# terms

id: MONDO:0000988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Discharge or drainage of fluid from the ear.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auditory system disorder","termid":"MONDO:0002409"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"discharging ear","secondary_identifiers":["DOID:10261","MEDGEN:57608","ICD9:388.60","UMLS:C0155540","ICD9:388.6"],"termid":"MONDO:0000988","xrefs":{"Monarch":{"xref_id":"0000988"}}}


id: PBO:0081736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF667 antisense RNA 1 (head to head)","termid":"PBO:0081736"}


id: PBO:0034322
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_evidence_for","termid":"PBO:0034322"}


id: GO:0047732
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: CDP-3,6-dideoxy-D-glucose = CDP-3,6-dideoxy-D-mannose.","definition_xrefs":["EC:5.1.3.10","RHEA:21656"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on carbohydrates and derivatives","termid":"GO:0016857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"CDP-abequose epimerase activity","secondary_identifiers":["MetaCyc:RXN-9160","KEGG_REACTION:R04266"],"synonyms":[{"name":"CDP-3,6-dideoxy-D-glucose 2-epimerase activity","type":"related"},{"name":"CDP-D-abequose 2-epimerase activity","type":"related"},{"name":"CDP-paratose 2-epimerase activity","type":"related"},{"name":"CDP-paratose epimerase activity","type":"related"},{"name":"CDP-tyvelose 2-epimerase activity","type":"related"},{"name":"cytidine diphosphate paratose-2-epimerase activity","type":"related"},{"name":"cytidine diphosphoabequose epimerase activity","type":"related"},{"name":"cytidine diphosphodideoxyglucose epimerase activity","type":"related"},{"name":"cytidine diphosphoparatose epimerase activity","type":"related"}],"termid":"GO:0047732"}


id: PBO:0082761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the SF3b subcomplex of the U2 snRNP; zinc cluster protein involved in pre-mRNA splicing and cycloheximide resistance","termid":"PBO:0082761"}


id: PBO:0114521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3-H4 chaperone, CAF assembly factor (CAF-1) complex WD repeat subunit C, Pcf3","termid":"PBO:0114521"}


id: MONDO:0008655
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vestibulocochlear dysfunction, progressive","secondary_identifiers":["MESH:C536346","MEDGEN:419730","OMIM:193005","UMLS:C2931176"],"synonyms":[{"name":"familial progressive vestibulocochlear dysfunction","type":"related"},{"name":"vestibulocochlear dysfunction, progressive","type":"exact"}],"termid":"MONDO:0008655","xrefs":{"Monarch":{"xref_id":"0008655"}}}


id: GO:0042418
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of epinephrine, a hormone produced by the medulla of the adrenal glands that increases heart activity, improves the power and prolongs the action of muscles, and increases the rate and depth of breathing. It is synthesized by the methylation of norepinephrine.","definition_xrefs":["ISBN:0192801023","GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epinephrine metabolic process","termid":"GO:0042414"},{"relation_name":"is_a","term_name":"catecholamine biosynthetic process","termid":"GO:0042423"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"epinephrine biosynthetic process","synonyms":[{"name":"adrenaline biosynthesis","type":"exact"},{"name":"adrenaline biosynthetic process","type":"exact"},{"name":"epinephrine anabolism","type":"exact"},{"name":"epinephrine biosynthesis","type":"exact"},{"name":"epinephrine formation","type":"exact"},{"name":"epinephrine synthesis","type":"exact"}],"termid":"GO:0042418"}


id: PBO:0064644
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPDPF pseudogene 1","termid":"PBO:0064644"}


id: GO:0050634
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: isovaleryl-CoA + 3 malonyl-CoA = 4 CoASH + 3 CO2 + 3-methyl-1-(2,4,6-trihydroxyphenyl)butan-1-one.","definition_xrefs":["EC:2.3.1.156","MetaCyc:2.3.1.156-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"phloroisovalerophenone synthase activity","secondary_identifiers":["RHEA:23572"],"synonyms":[{"name":"3-methyl-1-(trihydroxyphenyl)butan-1-one synthase activity","type":"related"},{"name":"isovaleryl-CoA:malonyl-CoA acyltransferase activity","type":"related"},{"name":"valerophenone synthase activity","type":"related"}],"termid":"GO:0050634"}


id: MONDO:0013084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroblastoma, susceptibility to, 4","secondary_identifiers":["UMLS:C2751680","OMIM:613015","MEDGEN:414082"],"synonyms":[{"name":"NBLST4","type":"exact"},{"name":"neuroblastoma, susceptibility to, 4","type":"exact"}],"termid":"MONDO:0013084","xrefs":{"Monarch":{"xref_id":"0013084"}}}


id: PBO:0001314
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed during sporulation","termid":"PBO:0001314"}


id: GO:0043896
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1->6)-alpha-D-glucosidic linkages in (1->6)-alpha-D-glucans and derived oligosaccharides.","definition_xrefs":["EC:3.2.1.70"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-glucosidase activity","termid":"GO:0090599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016798"],"is_obsolete":false,"name":"glucan 1,6-alpha-glucosidase activity","secondary_identifiers":["MetaCyc:3.2.1.70-RXN"],"synonyms":[{"name":"exo-1,6-alpha-glucosidase activity","type":"related"},{"name":"exo-1,6-beta-glucosidase","type":"related"},{"name":"glucan alpha-1,6-D-glucohydrolase activity","type":"related"},{"name":"glucan-1,6-alpha-glucosidase activity","type":"exact"},{"name":"glucodextranase activity","type":"related"},{"name":"glucodextrinase","type":"broad"}],"termid":"GO:0043896"}


id: MONDO:0006627
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete microscopic polyangiitis (obsolete MONDO:0006627)","termid":"MONDO:0006627","xrefs":{"Monarch":{"xref_id":"0006627"}}}


id: MONDO:0043099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"intellectual disability","termid":"MONDO:0001071"},{"relation_name":"is_a","term_name":"pulmonary valve stenosis","termid":"MONDO:0006936"},{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0005267"],"is_obsolete":false,"name":"Hordnes Engebretsen Knudtson syndrome","secondary_identifiers":["MESH:C536067","UMLS:C2931100","MEDGEN:419333","GARD:2736"],"synonyms":[{"name":"acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and intellectual disability","type":"related"},{"name":"acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and mental retardation","type":"related"}],"termid":"MONDO:0043099","xrefs":{"Monarch":{"xref_id":"0043099"}}}


id: PBO:0116787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFP69B divergent transcript","termid":"PBO:0116787"}


id: PR:O60083
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tfb6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1494.09c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1494.09c","synonyms":[{"name":"Spom972h-tfb6","type":"exact"}],"termid":"PR:O60083"}


id: PBO:0048322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 33","termid":"PBO:0048322"}


id: PBO:0049064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 79, pseudogene","termid":"PBO:0049064"}


id: GO:0018909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving dodecyl sulfate, commonly found as sodium dodecyl sulfate (SDS), a component of a variety of synthetic surfactants.","definition_xrefs":["UM-BBD_pathwayID:dds"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"xenobiotic metabolic process","termid":"GO:0006805"},{"relation_name":"is_a","term_name":"oxoacid metabolic process","termid":"GO:0043436"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"dodecyl sulfate metabolic process","synonyms":[{"name":"dodecyl sulfate metabolism","type":"exact"},{"name":"dodecyl sulphate metabolic process","type":"exact"},{"name":"dodecyl sulphate metabolism","type":"exact"}],"termid":"GO:0018909"}


id: GO:0097324
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of melanocytes from one site to another, often during the development of a multicellular organism. A melanocyte is a pigment cell derived from the neural crest. It contains melanin-filled pigment granules, which give a brown to black appearance.","definition_xrefs":["GOC:uh","PMID:22637532","CL:0000148"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell migration","termid":"GO:0010631"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"melanocyte migration","termid":"GO:0097324"}


id: GO:0017178
data:
  {"annotated_genes":["SJAG_04544"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77343],"is_not":false,"summary":null,"term":"GO:0017178"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + diphthine + NH4 = ADP + diphthamide + H+ + phosphate.","definition_xrefs":["RHEA:19753","EC:6.3.1.14"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-ammonia (or amide) ligase activity","termid":"GO:0016880"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04544":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"diphthine-ammonia ligase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R03613","MetaCyc:DIPHTINE--AMMONIA-LIGASE-RXN","Reactome:R-HSA-5358475"],"synonyms":[{"name":"diphthamide synthase activity","type":"related"},{"name":"diphthamide synthetase activity","type":"related"},{"name":"diphthine:ammonia ligase (ADP-forming)","type":"related"}],"termid":"GO:0017178","terms_by_termid":{"GO:0017178":null}}


id: MONDO:0001340
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the heart","direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular cancer","termid":"MONDO:0002100"},{"relation_name":"is_a","term_name":"thoracic cancer","termid":"MONDO:0003274"},{"relation_name":"is_a","term_name":"heart neoplasm","termid":"MONDO:0021209"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005267"],"is_obsolete":false,"name":"heart cancer","secondary_identifiers":["MESH:D006338","UMLS:C0153500","MEDGEN:57787","DOID:117","ICD9:164.1","NCIT:C3548"],"synonyms":[{"name":"Cardiac neoplasm, malignant","type":"exact"},{"name":"Cardiac tumor","type":"broad"},{"name":"Cardiac tumour","type":"broad"},{"name":"cancer of heart","type":"exact"},{"name":"heart cancer","type":"exact"},{"name":"malignant Cardiac neoplasm","type":"exact"},{"name":"malignant Cardiac tumor","type":"exact"},{"name":"malignant Cardiac tumour","type":"exact"},{"name":"malignant heart neoplasm","type":"exact"},{"name":"malignant heart tumor","type":"exact"},{"name":"malignant heart tumour","type":"exact"},{"name":"malignant neoplasm of heart","type":"exact"},{"name":"malignant neoplasm of the heart","type":"exact"},{"name":"malignant tumor of heart","type":"exact"},{"name":"malignant tumor of the heart","type":"exact"},{"name":"malignant tumour of heart","type":"exact"},{"name":"malignant tumour of the heart","type":"exact"},{"name":"tumor of heart","type":"broad"},{"name":"tumour of heart","type":"broad"}],"termid":"MONDO:0001340","xrefs":{"Monarch":{"xref_id":"0001340"}}}


id: PBO:0060199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MUC20 overlapping transcript","termid":"PBO:0060199"}


id: PBO:0086685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; identified by SAGE","termid":"PBO:0086685"}


id: GO:0050146
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a nucleotide + a 2'-deoxynucleoside = a nucleoside + a 2'-deoxynucleoside 5'-monophosphate.","definition_xrefs":["EC:2.7.1.77","MetaCyc:NUCLEOSIDE-PHOSPHOTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"nucleobase-containing compound kinase activity","termid":"GO:0019205"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"nucleoside phosphotransferase activity","secondary_identifiers":["Reactome:R-HSA-9754916","Reactome:R-HSA-2162066","RHEA:19961"],"synonyms":[{"name":"nonspecific nucleoside phosphotransferase activity","type":"related"},{"name":"nucleotide:2'-nucleoside 5'-phosphotransferase activity","type":"related"},{"name":"nucleotide:3'-deoxynucleoside 5'-phosphotransferase activity","type":"related"},{"name":"nucleotide:nucleoside 5'-phosphotransferase activity","type":"related"}],"termid":"GO:0050146"}


id: PBO:0018022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic septin Spn7","termid":"PBO:0018022"}


id: PBO:0080333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 97 pseudogene","termid":"PBO:0080333"}


id: PBO:0074349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMAD3 associated long non-coding RNA","termid":"PBO:0074349"}


id: PBO:0051225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (II)-1-1 (pseudogene)","termid":"PBO:0051225"}


id: PBO:0113040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chaperone for eEF1A; ribosome-associated chaperone dedicated to facilitating high-level expression of eEF1A; transiently binds nascent GTPase domain of eEF1A as soon as it emerges from ribosome tunnel; forms complex with NAC by binding UBA domain of Egd2p; inactivation results in disturbed proteostasis and Hsf1p activation due to abberant eEF1A biogenesis; overlapping phenotypes support notion that Chp1p functions in same eEF1A biogenesis pathway as chaperone Zpr1p-Aim29p","termid":"PBO:0113040"}


id: PBO:0017458
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-hyperparasitized_by","termid":"PBO:0017458"}


id: MONDO:0001290
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the small vessels of the skin that is mediated by the immune system.","definition_xrefs":["NCIT:C35119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atopic eczema","termid":"MONDO:0004980"},{"relation_name":"is_a","term_name":"hypersensitivity vasculitis","termid":"MONDO:0006794"},{"relation_name":"is_a","term_name":"cutaneous vasculitis","termid":"MONDO:0020576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"allergic cutaneous vasculitis","secondary_identifiers":["DOID:11450","MEDGEN:57718","UMLS:C0151436"],"synonyms":[{"name":"allergic cutaneous angiitis","type":"exact"},{"name":"autoimmune hypersensitivity angiitis","type":"exact"}],"termid":"MONDO:0001290","xrefs":{"Monarch":{"xref_id":"0001290"}}}


id: PR:Q02592
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-binding cassette sub-family B member 6, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heavy metal tolerance protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC737.09c","secondary_identifiers":["UniProtKB:Q02592"],"synonyms":[{"name":"Spom972h-ABCB6","type":"exact"}],"termid":"PR:Q02592"}


id: PBO:0047648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 4 pseudogene 1","termid":"PBO:0047648"}


id: PBO:0087869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional coactivator; bridges the DNA-binding region of Gcn4p and TATA-binding protein Spt15p; suppressor of frameshift mutations; protein abundance increases in response to DNA replication stress","termid":"PBO:0087869"}


id: FYPO:0004387
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which positive regulation of DNA-directed DNA polymerase activity occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah","PMID:14766746"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of catalytic activity","termid":"FYPO:0004916"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased positive regulation of DNA-directed DNA polymerase activity","synonyms":[{"name":"decreased activation of DNA-directed DNA polymerase activity","type":"narrow"},{"name":"decreased positive regulation of DNA polymerase activity","type":"broad"},{"name":"decreased positive regulation of DNA-directed DNA polymerase activity during mitotic cell cycle","type":"related"},{"name":"decreased positive regulation of DNA-directed DNA polymerase activity during vegetative growth","type":"exact"},{"name":"reduced positive regulation of DNA-directed DNA polymerase activity","type":"exact"}],"termid":"FYPO:0004387"}


id: MONDO:0007006
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disease involving the ulnar nerve from its origin in the brachial plexus to its termination in the hand. Clinical manifestations may include paresis or paralysis of wrist flexion, finger flexion, thumb adduction, finger abduction, and finger adduction. Sensation over the medial palm, fifth finger, and ulnar aspect of the ring finger may also be impaired. Common sites of injury include the axilla, cubital tunnel at the elbow, and Guyon's canal at the wrist. (From Joynt, Clinical Neurology, 1995, Ch51 pp43-5)","definition_xrefs":["MESH:D020424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mononeuropathy","termid":"MONDO:0001397"},{"relation_name":"is_a","term_name":"brachial plexus neuropathy","termid":"MONDO:0006683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"ulnar neuropathy","secondary_identifiers":["DOID:4613","SCTID:359837005","UMLS:C0154743","MEDGEN:57596","EFO:1001224"],"synonyms":[{"name":"mononeuropathy of ulnar nerve","type":"exact"},{"name":"ulnar nerve mononeuropathy","type":"exact"},{"name":"ulnar neuropathy","type":"exact"},{"name":"ulnar neuropathy (disorder) [ambiguous]","type":"exact"}],"termid":"MONDO:0007006","xrefs":{"Monarch":{"xref_id":"0007006"}}}


id: MONDO:0008420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A common benign skin neoplasm usually affecting older individuals. The lesions usually are multiple and arise in the face, chest, and shoulders. They appear as black or brown, slightly elevated skin lesions.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keratosis","termid":"MONDO:0006566"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"seborrheic keratosis","secondary_identifiers":["OMIM:182000","SCTID:398838000","MESH:D017492","UMLS:C0022603","Wikipedia:Seborrheic_keratosis","EFO:0005584","ICD10CM:L82","DOID:6498","ICD9:702.1","MEDGEN:5957","NCIT:C9006"],"synonyms":[{"name":"basal cell papilloma","type":"exact"},{"name":"keratosis Seborrheica","type":"exact"},{"name":"keratosis, seborrheic","type":"related"},{"name":"keratosis, seborrheic, somatic","type":"exact"}],"termid":"MONDO:0008420","xrefs":{"Monarch":{"xref_id":"0008420"}}}


id: GO:0004564
data:
  {"annotated_genes":["SJAG_04301"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004575"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a fructofuranosylated fructofuranosyl acceptor + H2O = a non fructofuranosylated fructofuranosyl acceptor + a beta-D-fructofuranoside.","definition_xrefs":["EC:3.2.1.26","MetaCyc:RXN-9985"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04301":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016798"],"is_obsolete":false,"name":"beta-fructofuranosidase activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"acid invertase activity","type":"broad"},{"name":"alkaline invertase activity","type":"broad"},{"name":"beta-D-fructofuranoside fructohydrolase activity","type":"exact"},{"name":"beta-fructosidase activity","type":"related"},{"name":"beta-h-fructosidase activity","type":"related"},{"name":"fructosylinvertase activity","type":"related"},{"name":"glucosucrase activity","type":"related"},{"name":"invertase activity","type":"broad"},{"name":"invertin activity","type":"broad"},{"name":"maxinvert L 1000 activity","type":"related"},{"name":"saccharase activity","type":"related"}],"termid":"GO:0004564","terms_by_termid":{"GO:0004575":null}}


id: MONDO:0017386
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant mesenchymal neoplasm with skeletal muscle differentiation, occurring in adults and rarely in children. The tumor is characterized by the presence of bizarre round, spindle, and polygonal cells. Clinical presentation includes a rapidly enlarging painful mass usually of the lower extremities.","definition_xrefs":["NCIT:C4258"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhabdomyosarcoma","termid":"MONDO:0005212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"pleomorphic rhabdomyosarcoma","secondary_identifiers":["SCTID:404054005","Orphanet:293199","ONCOTREE:PLRMS","UMLS:C0334480","MEDGEN:137770","DOID:3250","GARD:21165","ICD9:171.9"],"synonyms":[{"name":"anaplastic rhabdomyosarcoma","type":"exact"},{"name":"pleomorphic rhabdomyosarcoma","type":"exact"},{"name":"pleomorphic rhabdomyosarcoma, adult type","type":"exact"}],"termid":"MONDO:0017386","xrefs":{"Monarch":{"xref_id":"0017386"}}}


id: GO:0003277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process that contributes to the shaping of an endocardial cushion. The endocardial cushion is a specialized region of mesenchymal cells that will give rise to the heart septa and valves.","definition_xrefs":["GOC:mtg_heart","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process involved in heart morphogenesis","termid":"GO:0003278"},{"relation_name":"part_of","term_name":"endocardial cushion morphogenesis","termid":"GO:0003203"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"apoptotic process involved in endocardial cushion morphogenesis","synonyms":[{"name":"apoptosis involved in endocardial cushion morphogenesis","type":"narrow"}],"termid":"GO:0003277"}


id: PBO:0076837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TERF1 pseudogene 4","termid":"PBO:0076837"}


id: GO:0020028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of hemoglobin into a cell by receptor-mediated endocytosis.","definition_xrefs":["GOC:mb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor-mediated endocytosis","termid":"GO:0006898"},{"relation_name":"is_a","term_name":"protein transport","termid":"GO:0015031"},{"relation_name":"is_a","term_name":"establishment of protein localization to organelle","termid":"GO:0072594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"endocytic hemoglobin import into cell","synonyms":[{"name":"endocytic hemoglobin import","type":"related"},{"name":"haemoglobin uptake","type":"exact"},{"name":"hemoglobin uptake","type":"exact"}],"termid":"GO:0020028"}


id: FYPO:0005310
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which acetylation of lysine at position 14 of histone H3 occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K14 acetylation during vegetative growth","termid":"FYPO:0000788"},{"relation_name":"is_a","term_name":"increased histone H3 acetylation during vegetative growth","termid":"FYPO:0002363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0002494","FYPO:0000002","FYPO:0002274","FYPO:0005447"],"is_obsolete":false,"name":"increased histone H3-K14 acetylation during vegetative growth","synonyms":[{"name":"increased histone H3-K14 acetylation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0005310"}


id: MONDO:0025419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A persistent skin infection marked by the presence of furuncles, often chronic and recurrent. In salmonid fish (salmonids), the pathogen is Aeromonas salmonicida.","definition_xrefs":["MESH:D005667"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fish disease","termid":"MONDO:0024934"},{"relation_name":"is_a","term_name":"infectious disease, non-human animal","termid":"MONDO:0700049"},{"relation_name":"is_a","term_name":"inflammatory disease, non-human animal","termid":"MONDO:1011327"},{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"furunculosis, fish","secondary_identifiers":["icd11.foundation:1194531705","NCIT:C34629"],"synonyms":[{"name":"boils","type":"related"},{"name":"furuncle","type":"related"},{"name":"furuncles","type":"related"},{"name":"furunculoses","type":"related"}],"termid":"MONDO:0025419","xrefs":{"Monarch":{"xref_id":"0025419"}}}


id: SO:0001463
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Long, intervening non-coding RNA. A transcript that does not overlap within the start or end genomic coordinates of a coding gene or pseudogene on either strand.","definition_xrefs":["PMID:19182780","PMID:23463798","SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lncRNA","termid":"SO:0001877"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lincRNA","synonyms":[{"name":"large intervening non-coding RNA","type":"exact"},{"name":"long intergenic non-coding RNA","type":"exact"},{"name":"long intervening non-coding RNA","type":"exact"}],"termid":"SO:0001463"}


id: PBO:0040217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase family AAA domain containing 3B","termid":"PBO:0040217"}


id: PBO:0004268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inorganic phosphate transporter (predicted)","termid":"PBO:0004268"}


id: PBO:0062259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily D member 15 pseudogene","termid":"PBO:0062259"}


id: PR:Q9UT31
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug130 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UT31"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 130 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8F11.05c","synonyms":[{"name":"Spom972h-mug130","type":"exact"}],"termid":"PR:Q9UT31"}


id: PBO:0060565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBPF member 1","termid":"PBO:0060565"}


id: MONDO:0030071
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinitis pigmentosa 89","secondary_identifiers":["DOID:0112146","MEDGEN:1710499","UMLS:C5394552","OMIM:618955"],"synonyms":[{"name":"RETINITIS PIGMENTOSA 89","type":"exact"},{"name":"RP89","type":"exact"},{"name":"retinitis pigmentosa 89","type":"exact"}],"termid":"MONDO:0030071","xrefs":{"Monarch":{"xref_id":"0030071"}}}


id: PBO:0057692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1282","termid":"PBO:0057692"}


id: GO:0001842
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the neural fold is formed. The edges of the neural plate thicken and move up to form a U-shaped structure called the neural groove.","definition_xrefs":["ISBN:0878932437","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of embryonic epithelium","termid":"GO:0016331"},{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"is_a","term_name":"morphogenesis of an epithelial fold","termid":"GO:0060571"},{"relation_name":"part_of","term_name":"primary neural tube formation","termid":"GO:0014020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural fold formation","synonyms":[{"name":"neural groove formation","type":"related"}],"termid":"GO:0001842"}


id: FYPO:0002450
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that is septated and has abnormal morphology (i.e. size, shape, or structure), and that undergoes two or more rounds of cell division and then dies.","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, multiple cell divisions, abnormal morphology","termid":"FYPO:0002148"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0000005"],"is_obsolete":false,"name":"inviable after spore germination, multiple cell divisions, septated cell with abnormal morphology","synonyms":[{"name":"inviable following spore germination, multiple cell divisions, septated cell with abnormal morphology","type":"exact"},{"name":"inviable germinated spore, multiple cell divisions, septated cell with abnormal morphology","type":"exact"},{"name":"lethal after spore germination, multiple cell divisions, septated cell with abnormal morphology","type":"exact"}],"termid":"FYPO:0002450"}


id: GO:0140293
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (ADP-D-ribosyl)-L-glutamyl-[protein] + H2O = L-glutamyl-[protein] + ADP-ribose.","definition_xrefs":["PMID:23481255"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing N-glycosyl compounds","termid":"GO:0016799"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0140096","GO:0016787","GO:0016798","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"ADP-ribosylglutamate hydrolase activity","termid":"GO:0140293"}


id: GO:0003323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a type B pancreatic cell over time, from its formation to the mature structure. A type B pancreatic cell is a cell located towards center of the islets of Langerhans that secretes insulin.","definition_xrefs":["GOC:dph","CL:0000169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell development","termid":"GO:0002064"},{"relation_name":"part_of","term_name":"type B pancreatic cell differentiation","termid":"GO:0003309"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"type B pancreatic cell development","synonyms":[{"name":"pancreatic B cell development","type":"exact"},{"name":"pancreatic beta cell development","type":"exact"}],"termid":"GO:0003323"}


id: PBO:0076447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAFA chemokine like family member 3","termid":"PBO:0076447"}


id: PBO:0002067
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Berardinelli-Seip congenital lipodystrophy type 2, Silver spastic paraplegia syndrome, distal hereditary motor neuropathy type V","termid":"PBO:0002067"}


id: GO:0097667
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An SCF ubiquitin ligase complex in which the F-box protein is Rcy1 in S. cerevisiae (Pof6 in S. pombe).","definition_xrefs":["PMID:15147268","GOC:jd","PMID:14747994","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SCF ubiquitin ligase complex","termid":"GO:0019005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"SCF-Rcy1/Pof6 ubiquitin ligase complex","termid":"GO:0097667"}


id: PBO:0083217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps verified gene ARO9/YHR137W; identified by gene-trapping, expression analysis, and genome-wide homology searching","termid":"PBO:0083217"}


id: PBO:0039639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde oxidase 2, pseudogene","termid":"PBO:0039639"}


id: GO:0033266
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O = ADP + phosphate, to directly drive the transport of choline across a membrane.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choline transmembrane transporter activity","termid":"GO:0015220"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"ABC-type choline transporter activity","synonyms":[{"name":"ABC-type choline transmembrane transporter activity","type":"exact"},{"name":"ATP-dependent choline transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled choline transmembrane transporter activity","type":"related"},{"name":"choline-transporting ATPase activity","type":"related"}],"termid":"GO:0033266"}


id: PR:Q10435
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An E3 ubiquitin-protein ligase TRIP12 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01893","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin fusion degradation protein C12B10.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC12B10.01c","secondary_identifiers":["UniProtKB:Q10435"],"synonyms":[{"name":"Spom972h-TRIP12","type":"exact"}],"termid":"PR:Q10435"}


id: GO:0036489
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of neuromelanin. Neuromelanin is a polymer of 5,6-dihydroxyindole monomers.","definition_xrefs":["GOC:bf","Wiki:Neuromelanin","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neuromelanin biosynthetic process","synonyms":[{"name":"neuromelanin anabolism","type":"exact"},{"name":"neuromelanin biosynthesis","type":"exact"},{"name":"neuromelanin formation","type":"exact"},{"name":"neuromelanin synthesis","type":"exact"}],"termid":"GO:0036489"}


id: MONDO:0004142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of large cell neuroendocrine lung carcinoma characterized by the presence of large neuroendocrine cells in combination with adenocarcinoma, squamous cell carcinoma, giant cell carcinoma and/ or spindle cell carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary large cell neuroendocrine carcinoma","termid":"MONDO:0003960"},{"relation_name":"is_a","term_name":"combined lung carcinoma","termid":"MONDO:0006167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"lung combined large cell neuroendocrine carcinoma","secondary_identifiers":["DOID:7207","UMLS:C1333122","MEDGEN:232386","NCIT:C7267"],"synonyms":[{"name":"combined large cell lung neuroendocrine carcinoma","type":"exact"},{"name":"combined large cell neuroendocrine carcinoma of lung","type":"exact"},{"name":"combined large cell neuroendocrine carcinoma of the lung","type":"exact"},{"name":"pulmonary combined large cell neuroendocrine carcinoma","type":"exact"}],"termid":"MONDO:0004142","xrefs":{"Monarch":{"xref_id":"0004142"}}}


id: MONDO:0011769
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete familial aortic dissection (obsolete MONDO:0011769)","termid":"MONDO:0011769","xrefs":{"Monarch":{"xref_id":"0011769"}}}


id: PBO:0029332
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H2A_phosphorylation","termid":"PBO:0029332"}


id: GO:0140122
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Lewy body formation.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of inclusion body assembly","termid":"GO:0090083"},{"relation_name":"regulates","term_name":"Lewy body formation","termid":"GO:0140121"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"regulation of Lewy body formation","termid":"GO:0140122"}


id: GO:0044764
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that is carried out at the cellular level which involves another organism of the same or different species.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete multi-organism cellular process (obsolete GO:0044764)","termid":"GO:0044764"}


id: PR:Q9UT74
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- lys2 gene.","definition_xrefs":["UniProtKB:Q9UT74","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homoaconitase, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC343.16","synonyms":[{"name":"Spom972h-lys2","type":"exact"},{"name":"homoaconitate hydratase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT74"}


id: GO:0106332
data:
  {"annotated_genes":["SJAG_05237"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[101498],"is_not":false,"summary":null,"term":"GO:0106332"}]},"cv_name":"molecular_function","definition":"Catalysis of the endonucleolytic cleavage of double-stranded DNA near a double-strand/single-strand DNA junction.","definition_xrefs":["PMID:14528010"],"direct_ancestors":[{"relation_name":"is_a","term_name":"double-stranded DNA endonuclease activity","termid":"GO:1990238"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05237":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0140097","GO:0016788","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"ds/ssDNA junction-specific dsDNA endonuclease activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0106332","terms_by_termid":{"GO:0106332":null}}


id: PBO:0057485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 603","termid":"PBO:0057485"}


id: PBO:0060232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloid associated differentiation marker like 2","termid":"PBO:0060232"}


id: PBO:0030248
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_cold","termid":"PBO:0030248"}


id: GO:0120333
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The radial spoke of each group of radial spokes, whether grouped as triplets or doublets, that is most proximal to the base of the cilium. Radial spoke 1 (RS1), similarly to radial spoke 2, is comprised of four domains: 1) a very short base anchored to the A microtubule, 2) an elongaged stalk, 3) a bifurcated neck, and 4) an orthogonal head. The base of RS1 is connected to the tail of the inner dynein arm a/d.","definition_xrefs":["GOC:krc","PMID:22754630"],"direct_ancestors":[{"relation_name":"is_a","term_name":"radial spoke","termid":"GO:0001534"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"radial spoke 1","synonyms":[{"name":"RS1","type":"related"}],"termid":"GO:0120333"}


id: PBO:0052521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 34","termid":"PBO:0052521"}


id: PBO:0052772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 64","termid":"PBO:0052772"}


id: PBO:0034173
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-results_in_transport_to_from_or_in","termid":"PBO:0034173"}


id: PBO:0071486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 27","termid":"PBO:0071486"}


id: MONDO:0021130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of sphingolipid biosynthetic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"disorder of sphingolipid biosynthesis","synonyms":[{"name":"inborn error of sphingolipid biosynthetic process","type":"exact"},{"name":"inborn sphingolipid biosynthetic process disorder","type":"exact"},{"name":"rare inborn error of sphingolipid biosynthetic process","type":"exact"}],"termid":"MONDO:0021130","xrefs":{"Monarch":{"xref_id":"0021130"}}}


id: MONDO:0013139
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant severe congenital neutropenia in which the cause of the disease is a mutation in the GFI1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant severe congenital neutropenia","termid":"MONDO:0008742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"neutropenia, severe congenital, 2, autosomal dominant","secondary_identifiers":["GARD:15616","DOID:0112131","OMIM:613107","MESH:C567748","MEDGEN:413975","UMLS:C2751288"],"synonyms":[{"name":"GFI1 autosomal dominant severe congenital neutropenia","type":"exact"},{"name":"SCN2","type":"related"},{"name":"autosomal dominant severe congenital neutropenia caused by mutation in GFI1","type":"exact"},{"name":"neutropenia, severe congenital 2, autosomal dominant","type":"exact"},{"name":"neutropenia, severe congenital, 2, autosomal dominant","type":"exact"}],"termid":"MONDO:0013139","xrefs":{"Monarch":{"xref_id":"0013139"}}}


id: PBO:0086035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function found in mitochondria; expression is regulated by transcription factors involved in pleiotropic drug resistance, Pdr1p and Yrr1p; not an essential gene; YLR346C has a paralog, YGR035C, that arose from the whole genome duplication","termid":"PBO:0086035"}


id: PBO:0046523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endoplasmic reticulum metallopeptidase 1","termid":"PBO:0046523"}


id: PBO:0075883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST6 beta-galactoside alpha-2,6-sialyltransferase 1","termid":"PBO:0075883"}


id: PBO:0064900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 regulatory subunit B'epsilon","termid":"PBO:0064900"}


id: MONDO:0017134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Odonto-onycho dysplasia-alopecia syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by almost total alopecia with only sparse, thin, brittle, slow-growing scalp hair, fair and sparse eyebrows and eyelashes, absent axillary and pubic hair, fragile and brittle fingernails, thick and brittle toenails (both with a subungual corneal layer), hypodontia, microdontia, widely spaced teeth with hypoplastic enamel, mild palmoplantar keratosis, cafe-au-lait spots and areolae anomalies. There have been no further descriptions in the literature since 1985.","definition_xrefs":["Orphanet:2722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"odonto-onycho dysplasia-alopecia syndrome","secondary_identifiers":["MEDGEN:1648007","UMLS:C4706599","GARD:4051"],"synonyms":[{"name":"odonto onycho dysplasia with alopecia","type":"related"}],"termid":"MONDO:0017134","xrefs":{"Monarch":{"xref_id":"0017134"}}}


id: GO:0031578
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A signaling process that monitors and signals errors in the placement or orientation of the spindle in the cell. This delays the completion of anaphase until errors are corrected.","definition_xrefs":["GOC:mtg_cell_cycle","PMID:14616062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of exit from mitosis","termid":"GO:0001100"},{"relation_name":"is_a","term_name":"mitotic spindle checkpoint signaling","termid":"GO:0071174"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0044772"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044772"}],"interesting_parent_ids":["GO:0007049","GO:0023052","GO:0008150","GO:0044772"],"is_obsolete":false,"name":"mitotic spindle orientation checkpoint signaling","secondary_identifiers":["GO:0072483"],"synonyms":[{"name":"SOC","type":"exact"},{"name":"SPOC","type":"exact"},{"name":"mitotic cell cycle spindle orientation checkpoint","type":"exact"},{"name":"mitotic spindle orientation checkpoint","type":"exact"},{"name":"signal transduction involved in mitotic cell cycle spindle orientation checkpoint","type":"exact"},{"name":"spindle position checkpoint","type":"exact"}],"termid":"GO:0031578"}


id: MONDO:0017448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital absence/hypoplasia of fingers excluding thumb (obsolete MONDO:0017448)","secondary_identifiers":["Orphanet:294990"],"synonyms":[{"name":"digits 2-5 hypodactyly","type":"exact"},{"name":"digits 2-5 oligodactyly","type":"exact"}],"termid":"MONDO:0017448","xrefs":{"Monarch":{"xref_id":"0017448"}}}


id: GO:0098658
data:
  {"annotated_genes":["SJAG_02463"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902434"}]},"cv_name":"biological_process","definition":"The directed movement of inorganic anions from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inorganic anion transmembrane transport","termid":"GO:0098661"},{"relation_name":"is_a","term_name":"inorganic ion import across plasma membrane","termid":"GO:0099587"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02463":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"inorganic anion import across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"inorganic anion import into cell","type":"exact"}],"termid":"GO:0098658","terms_by_termid":{"GO:1902434":null}}


id: PBO:0000260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein disulfide isomerase (predicted)","termid":"PBO:0000260"}


id: MONDO:0004250
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenoma that arises from the extrahepatic bile ducts. It is characterized by the presence of a papillary growth pattern.","definition_xrefs":["NCIT:C5849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary adenoma","termid":"MONDO:0002533"},{"relation_name":"is_a","term_name":"extrahepatic bile duct adenoma","termid":"MONDO:0003445"},{"relation_name":"is_a","term_name":"bile duct papillary neoplasm","termid":"MONDO:0003455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"extrahepatic bile duct papillary adenoma","secondary_identifiers":["MEDGEN:232483","DOID:7503","UMLS:C1333510"],"synonyms":[{"name":"extrahepatic bile duct papillary adenoma","type":"exact"},{"name":"papillary adenoma of extrahepatic bile duct","type":"exact"},{"name":"papillary adenoma of the extrahepatic bile duct","type":"exact"}],"termid":"MONDO:0004250","xrefs":{"Monarch":{"xref_id":"0004250"}}}


id: PBO:0005255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphomethylpyrimidine kinase (predicted)","termid":"PBO:0005255"}


id: PBO:0042248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine receptor 10","termid":"PBO:0042248"}


id: GO:1901005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of ubiquinone-6.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete ubiquinone-6 catabolic process (obsolete GO:1901005)","synonyms":[{"name":"ubiquinone-6 breakdown","type":"exact"},{"name":"ubiquinone-6 catabolism","type":"exact"},{"name":"ubiquinone-6 degradation","type":"exact"}],"termid":"GO:1901005"}


id: GO:0070532
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the BRCA1-BARD1 heterodimer, BACH1 and TopBP1, and binds to DNA during S phase at DNA damage sites.","definition_xrefs":["GOC:mah","PMID:16391231"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0032991"],"is_obsolete":false,"name":"BRCA1-B complex","termid":"GO:0070532"}


id: GO:0043879
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of glycolate from one side of a membrane to the other. Glycolate is the smallest alpha-hydroxy acid (AHA).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transmembrane transporter activity","termid":"GO:0008028"},{"relation_name":"is_a","term_name":"alcohol transmembrane transporter activity","termid":"GO:0015665"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"glycolate transmembrane transporter activity","synonyms":[{"name":"glcA","type":"related"},{"name":"glycolate permease","type":"related"},{"name":"glycolic acid transmembrane transporter activity","type":"exact"},{"name":"hydroxyacetic acid transmembrane transporter activity","type":"exact"}],"termid":"GO:0043879"}


id: MONDO:0011131
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"tricho-oculo-dermo-vertebral syndrome","secondary_identifiers":["UMLS:C1866427","icd11.foundation:1206025469","MEDGEN:355714","OMIM:601701","Orphanet:3354","MESH:C537441"],"synonyms":[{"name":"Alves syndrome","type":"related"},{"name":"Alves-dos Santos-Castelo syndrome","type":"exact"},{"name":"Todv syndrome","type":"related"},{"name":"Trichooculodermovertebral syndrome","type":"related"},{"name":"arthrogryposis and ectodermal dysplasia","type":"related"},{"name":"ectodermal dysplasia - cataracts - kyphoscoliosis","type":"related"},{"name":"ectodermal dysplasia-cataracts-kyphoscoliosis syndrome","type":"exact"}],"termid":"MONDO:0011131","xrefs":{"Monarch":{"xref_id":"0011131"}}}


id: GO:0033096
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The double lipid bilayer enclosing the amyloplast and separating its contents from the rest of the cytoplasm; includes the intermembrane space.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid envelope","termid":"GO:0009526"},{"relation_name":"part_of","term_name":"amyloplast","termid":"GO:0009501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"amyloplast envelope","termid":"GO:0033096"}


id: PBO:0003020
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"possible frameshifts","termid":"PBO:0003020"}


id: GO:0099167
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic specialization membrane of a symmetric synapse consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of postsynaptic specialization membrane of symmetric synapse (obsolete GO:0099167)","termid":"GO:0099167"}


id: MONDO:0016866
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"},{"relation_name":"is_a","term_name":"chromosome 1 disorder","termid":"MONDO:0700008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of chromosome 1","secondary_identifiers":["Orphanet:261766","UMLS:C5679647","MEDGEN:1825957","GARD:20789"],"synonyms":[{"name":"partial deletion of chromosome type 1","type":"exact"},{"name":"partial monosomy of chromosome 1","type":"exact"}],"termid":"MONDO:0016866","xrefs":{"Monarch":{"xref_id":"0016866"}}}


id: GO:0033480
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of UDP-D-galacturonate, a substance composed of galacturonic acid in glycosidic linkage with uridine diphosphate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar biosynthetic process","termid":"GO:0009226"},{"relation_name":"is_a","term_name":"UDP-D-galacturonate metabolic process","termid":"GO:0033479"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"UDP-D-galacturonate biosynthetic process","secondary_identifiers":["MetaCyc:PWY-4"],"synonyms":[{"name":"UDP-D-galacturonate anabolism","type":"exact"},{"name":"UDP-D-galacturonate biosynthesis","type":"exact"},{"name":"UDP-D-galacturonate formation","type":"exact"},{"name":"UDP-D-galacturonate synthesis","type":"exact"}],"termid":"GO:0033480"}


id: MONDO:0858998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mesomelic dysplasia-digital anomalies-intellectual disability syndrome","secondary_identifiers":["Orphanet:632603","UMLS:C5816803","MEDGEN:1843408"],"termid":"MONDO:0858998","xrefs":{"Monarch":{"xref_id":"0858998"}}}


id: PBO:0087017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribonucleotide reductase inhibitor; intrinsically disordered protein that binds to and inhibits Rnr2p; involved in the Mec1p-mediated checkpoint pathway; transcription is induced by genotoxic stress and by activation of the Rad53p pathway; protein abundance increases in response to DNA replication stress","termid":"PBO:0087017"}


id: PBO:0042687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cat eye syndrome chromosome region","termid":"PBO:0042687"}


id: PBO:0057149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 297","termid":"PBO:0057149"}


id: MONDO:0021303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A adenoma that involves the small intestine.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small intestine neoplasm","termid":"MONDO:0004251"},{"relation_name":"is_a","term_name":"digestive system adenoma","termid":"MONDO:0006180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"adenoma of small intestine","secondary_identifiers":["NCIT:C5340","SCTID:399422005","MEDGEN:226995","UMLS:C1302392"],"synonyms":[{"name":"adenoma of small bowel","type":"exact"},{"name":"adenoma of the small bowel","type":"exact"},{"name":"adenoma of the small intestine","type":"exact"},{"name":"small bowel adenoma","type":"exact"},{"name":"small intestinal adenoma","type":"exact"},{"name":"small intestine adenoma","type":"exact"}],"termid":"MONDO:0021303","xrefs":{"Monarch":{"xref_id":"0021303"}}}


id: MONDO:0022921
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete short stature-microcephaly-heart defect syndrome (obsolete MONDO:0022921)","secondary_identifiers":["Orphanet:2861"],"synonyms":[{"name":"d'ercole syndrome","type":"related"},{"name":"short stature microcephaly heart defect","type":"related"}],"termid":"MONDO:0022921","xrefs":{"Monarch":{"xref_id":"0022921"}}}


id: FYPO:0003148
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase activity","termid":"FYPO:0003147"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000654","FYPO:0000661","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"increased UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase activity","termid":"FYPO:0003148"}


id: PBO:0042041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 92B","termid":"PBO:0042041"}


id: MONDO:0020324
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intravascular large B-cell lymphoma (IVLBCL) is a very rare form of diffuse large B-cell lymphoma characterized by the selective growth of lymphoma cells within the lumina of small blood vessels (especially the capillaries) that most often presents with a wide range of clinical manifestations (as potentially any tissue can be involved), with patients from Western countries more frequently manifesting with neurological and cutaneous symptoms while patients from Asian countries more frequently displaying hepatosplenomegaly and thrombocytopenia. IVLBCL is characterized by an absence of lymphadenopathy, an aggressive clinical course and a poor prognosis.","definition_xrefs":["Orphanet:98839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"intravascular large B-cell lymphoma","secondary_identifiers":["NCIT:C4342","ICD9:202.80","MedDRA:10069643","ICDO:9712/3","icd11.foundation:952730197","DOID:0081311","UMLS:C0334660","SCTID:255102004","GARD:19590","ONCOTREE:IVBCL","MEDGEN:90821"],"synonyms":[{"name":"IVBCL","type":"related"},{"name":"Tappeiner-Pfleger disease","type":"exact"},{"name":"angioendotheliomatosis proliferans systemisata","type":"exact"},{"name":"angiotropic large cell lymphoma","type":"exact"},{"name":"angiotropic lymphoma","type":"exact"},{"name":"intravascular B-cell lymphoma","type":"exact"},{"name":"intravascular large B-cell lymphoma","type":"exact"},{"name":"intravascular lymphomatosis","type":"exact"},{"name":"malignant angioendotheliomatosis","type":"exact"}],"termid":"MONDO:0020324","xrefs":{"Monarch":{"xref_id":"0020324"}}}


id: GO:0031840
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 2 neuromedin U receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuromedin U receptor binding","termid":"GO:0042922"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"type 2 neuromedin U receptor binding","synonyms":[{"name":"type 2 neuromedin U receptor ligand","type":"narrow"}],"termid":"GO:0031840"}


id: SO:0002067
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A deletion of the HERV mobile element with respect to a reference.","definition_xrefs":["NCBI:th"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"Endogenous_Retrovirus_LTR_retrotransposon","termid":"SO:0002268"},{"relation_name":"is_a","term_name":"mobile_element_deletion","termid":"SO:0002066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERV_deletion","synonyms":[{"name":"HERV deletion","type":"exact"}],"termid":"SO:0002067"}


id: PBO:0013816
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae TOP2","termid":"PBO:0013816"}


id: PBO:0027295
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_tetranucleate_vegetative_cell","termid":"PBO:0027295"}


id: GO:0032423
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mismatch repair.","definition_xrefs":["GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA repair","termid":"GO:0006282"},{"relation_name":"regulates","term_name":"mismatch repair","termid":"GO:0006298"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006281"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0006281","GO:0008150"],"is_obsolete":false,"name":"regulation of mismatch repair","termid":"GO:0032423"}


id: GO:0044388
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a small protein activating enzyme, such as ubiquitin-activating enzyme.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"small protein activating enzyme binding","termid":"GO:0044388"}


id: MOD:00757
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-proline residue to O4-galactosyl-L-hydroxyproline.","definition_xrefs":["RESID:AA0389"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O4-galactosyl-L-hydroxyproline","synonyms":[{"name":"(2S,4R)-4-(beta-D-galactopyranosyloxy)pyrrolidine-2-carboxylic acid","type":"exact"},{"name":"4-(beta-D-galactopyranosyloxy)proline","type":"exact"},{"name":"4-(galactosyloxy)proline","type":"exact"},{"name":"CARBOHYD O-linked (Gal) hydroxyproline","type":"exact"},{"name":"O4-galactosyl-L-hydroxyproline","type":"exact"},{"name":"O4-glycosyl-hydroxyproline","type":"exact"},{"name":"beta-galactopyranosyl-4-hydroxyproline","type":"exact"}],"termid":"MOD:00757"}


id: PBO:0070921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 29","termid":"PBO:0070921"}


id: PBO:0071366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 25","termid":"PBO:0071366"}


id: PBO:0113145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-binding protein of the rho subfamily of Ras-like small GTPases; involved in establishment of cell polarity; regulates protein kinase C (Pkc1p); positive regulatory subunit of the 1,3-beta-D-glucan synthase complex, activating 1,3-beta-glucan synthase (Fks1p and Gsc2p), an enzyme involved in cell wall biosynthesis","termid":"PBO:0113145"}


id: FYPO:0001622
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-threonine measured in the vacuole is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in vacuole","termid":"FYPO:0001603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001312","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal vacuolar threonine level","synonyms":[{"name":"normal level of threonine in vacuole","type":"exact"},{"name":"normal vacuolar L-threonine level","type":"exact"},{"name":"normal vacuolar threonine level during mitotic cell cycle","type":"related"},{"name":"normal vacuolar threonine level during vegetative growth","type":"exact"}],"termid":"FYPO:0001622"}


id: PBO:0029304
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cell_wall","termid":"PBO:0029304"}


id: PBO:0055186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2610","termid":"PBO:0055186"}


id: GO:0052050
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An interaction with the host organism mediated by a substance secreted by the other organism by a type IV secretion system. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete interaction with host via substance secreted by type IV secretion system (obsolete GO:0052050)","termid":"GO:0052050"}


id: PBO:0073736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC1A3 antisense RNA 1","termid":"PBO:0073736"}


id: FYECO:0000321
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which a copper chelator was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ copper chelator","synonyms":[{"name":"+ tetrathiomolybdate","type":"narrow"}],"termid":"FYECO:0000321"}


id: PBO:0047292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acyl-CoA reductase 1 pseudogene 1","termid":"PBO:0047292"}


id: GO:0031480
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A myosin complex containing one or more class X myosin heavy chains and associated light chains.","definition_xrefs":["PMID:27580874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unconventional myosin complex","termid":"GO:0016461"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0015629"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0015629"],"is_obsolete":false,"name":"myosin X complex","termid":"GO:0031480"}


id: PBO:0062379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily D member 1 pseudogene","termid":"PBO:0062379"}


id: FYPO:0004356
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the nucleolus is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to nucleus during vegetative growth","termid":"FYPO:0001130"},{"relation_name":"is_a","term_name":"abnormal protein localization to nucleolus","termid":"FYPO:0003687"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"increased protein localization to nucleolus","synonyms":[{"name":"increased protein localisation to nucleolus","type":"exact"},{"name":"increased protein localization to nucleolus during mitotic cell cycle","type":"related"},{"name":"increased protein localization to nucleolus during vegetative growth","type":"exact"}],"termid":"FYPO:0004356"}


id: FYPO:0004657
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, and has one nucleus and more than one septum.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"multiseptate vegetative cell","termid":"FYPO:0000118"},{"relation_name":"is_a","term_name":"multiseptate vegetative cell","termid":"FYPO:0000118"},{"relation_name":"is_a","term_name":"inviable mononucleate vegetative cell","termid":"FYPO:0006430"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0000631","FYPO:0000002","FYPO:0005447","FYPO:0000004","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"inviable mononucleate multiseptate vegetative cell","secondary_identifiers":["FYPO:0002001"],"synonyms":[{"name":"cytokinesis in the absence of nuclear division","type":"related"},{"name":"cytokinesis without nuclear division","type":"related"},{"name":"inviable mononucleate multiseptate cell during vegetative growth","type":"exact"},{"name":"inviable mononucleate multiseptate vegetative cell during mitotic cell cycle","type":"related"},{"name":"lethal; mononucleate multiseptate vegetative cell","type":"exact"},{"name":"mononucleate multiseptate vegetative cell","type":"exact"},{"name":"mononucleate multiseptate vegetative cell during mitotic cell cycle","type":"related"},{"name":"septation in the absence of nuclear division","type":"related"},{"name":"septation independent of mitosis","type":"related"},{"name":"septation without nuclear division","type":"related"},{"name":"vegetative cell with premature septation","type":"related"}],"termid":"FYPO:0004657"}


id: PBO:0058963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"makorin ring finger protein 6, pseudogene","termid":"PBO:0058963"}


id: PBO:0030315
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_myristoyl-CoA_ligase_activity","termid":"PBO:0030315"}


id: GO:0048370
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the lateral mesoderm. This process pertains to the initial formation of the structure from unspecified parts.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesoderm formation","termid":"GO:0001707"},{"relation_name":"part_of","term_name":"lateral mesoderm morphogenesis","termid":"GO:0048369"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral mesoderm formation","secondary_identifiers":["Reactome:R-HSA-9758920"],"synonyms":[{"name":"lateral plate mesoderm biosynthesis","type":"exact"},{"name":"lateral plate mesoderm formation","type":"exact"}],"termid":"GO:0048370"}


id: PBO:0070368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY5 pseudogene 6","termid":"PBO:0070368"}


id: MONDO:1012818
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital hypotrichosis that occurs in cats due to a mutation in the HR gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypotrichosis, non-human animal","termid":"MONDO:1012977"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis, HR-related, domestic cat","secondary_identifiers":["OMIA:002229-9685"],"termid":"MONDO:1012818","xrefs":{"Monarch":{"xref_id":"1012818"}}}


id: PBO:0031426
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_tert-butyl_hydroperoxide","termid":"PBO:0031426"}


id: MONDO:0017826
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-functioning pituitary adenoma","termid":"MONDO:0019613"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"null pituitary adenoma","secondary_identifiers":["MEDGEN:1813085","GARD:21393","ICD10CM:D35.2","UMLS:C5680967","Orphanet:314790","NCIT:C45924"],"termid":"MONDO:0017826","xrefs":{"Monarch":{"xref_id":"0017826"}}}


id: PBO:0084454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mannosylinositol phosphorylceramide (MIPC) synthase catalytic subunit; forms a complex with regulatory subunit Csg2p; function in sphingolipid biosynthesis is overlapping with that of Sur1p; CSH1 has a paralog, SUR1, that arose from the whole genome duplication","termid":"PBO:0084454"}


id: PBO:0088608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-I ortholog, inner centromere connector Mis6","termid":"PBO:0088608"}


id: GO:0019935
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An intracellular signaling cassette that starts with production or release of the cyclic nucleotide, and ends with the activation of downstream effectors that further transmit the signal within the cell.","definition_xrefs":["GOC:signaling"],"gene_count":0,"genotype_count":0,"name":"obsolete cyclic-nucleotide-mediated signaling (obsolete GO:0019935)","synonyms":[{"name":"cyclic-nucleotide-mediated signalling","type":"exact"}],"termid":"GO:0019935"}


id: PBO:0051356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2/OR2-8 (pseudogene)","termid":"PBO:0051356"}


id: PBO:0078930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon CCG) 1-2","termid":"PBO:0078930"}


id: GO:0031872
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1 proteinase activated receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteinase activated receptor binding","termid":"GO:0031871"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"type 1 proteinase activated receptor binding","synonyms":[{"name":"thrombin receptor binding","type":"exact"},{"name":"type 1 proteinase activated receptor ligand","type":"narrow"}],"termid":"GO:0031872"}


id: PBO:0080167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"voltage dependent anion channel 1 pseudogene 2","termid":"PBO:0080167"}


id: MONDO:0008631
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete renal agenesis (obsolete MONDO:0008631)","termid":"MONDO:0008631","xrefs":{"Monarch":{"xref_id":"0008631"}}}


id: FYPO:0000338
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the position or morphology of the mitotic spindle is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle","termid":"FYPO:0000120"},{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000120","FYPO:0000054","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0002399"],"is_obsolete":false,"name":"abnormal mitotic spindle","secondary_identifiers":["FYPO:0000277"],"synonyms":[{"name":"abnormal mitotic spindle during vegetative growth","type":"exact"},{"name":"abnormal spindle during mitotic cell cycle","type":"related"},{"name":"mitotic spindle defects","type":"exact"},{"name":"spindle polarity defects","type":"related"}],"termid":"FYPO:0000338"}


id: FYPO:0006884
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the mitotic spindle is thicker than normal during mitotic metaphase.","definition_xrefs":["PomBase:mah","PMID:30463883"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal bipolar mitotic spindle","termid":"FYPO:0001574"},{"relation_name":"is_a","term_name":"abnormal spindle morphology","termid":"FYPO:0003607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002399","FYPO:0001320","FYPO:0000120","FYPO:0005447","FYPO:0001985","FYPO:0000054"],"is_obsolete":false,"name":"thick mitotic spindle during mitotic metaphase","synonyms":[{"name":"increased mitotic spindle thickness during mitotic metaphase","type":"exact"},{"name":"thick mitotic spindle during mitotic metaphase during vegetative growth","type":"exact"},{"name":"thick spindle during mitotic metaphase of mitotic cell cycle","type":"exact"}],"termid":"FYPO:0006884"}


id: PBO:0072490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 19","termid":"PBO:0072490"}


id: PBO:0004387
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermine family transmembrane transporter Caf5","termid":"PBO:0004387"}


id: _global:is_bearer_of
data:
  {"annotation_feature_type":"gene","cv_name":"fypo_extension_relations","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_bearer_of","secondary_identifiers":["BFO:0000053"],"synonyms":[{"name":"has_color","type":"narrow"}],"termid":"_global:is_bearer_of"}


id: GO:0097696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An intracellular signal transduction process in which STAT proteins (Signal Transducers and Activators of Transcription) convey a signal to trigger a change in the activity or state of a cell. The STAT cascade begins with receptor activation followed by activation of STAT proteins by kinases. It proceeds through STA dimerization and subsequent nuclear translocation of STAT proteins, and ends with regulation of target gene expression by STAT proteins.","definition_xrefs":["PMID:21534947","GOC:rjd","PMID:24587195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway","termid":"GO:0007166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"cell surface receptor signaling pathway via STAT","synonyms":[{"name":"STAT signalling pathway","type":"exact"},{"name":"kinase activated-STAT cascade","type":"exact"},{"name":"kinase-STAT cascade","type":"exact"},{"name":"receptor signaling pathway via STAT","type":"exact"}],"termid":"GO:0097696"}


id: MONDO:0017242
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cutaneous collagenous vasculopathy (CCV) is a primary microangiopathy confined to the skin, characterized by multiple and widespread telangiectasias.","definition_xrefs":["Orphanet:280779"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin vascular disease","termid":"MONDO:0019293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"cutaneous collagenous vasculopathy","secondary_identifiers":["MEDGEN:930992","UMLS:C4305323","icd11.foundation:878108553","GARD:12428","SCTID:718634003"],"synonyms":[{"name":"CCV","type":"exact"},{"name":"cutaneus colagenous vasculopathy","type":"related"}],"termid":"MONDO:0017242","xrefs":{"Monarch":{"xref_id":"0017242"}}}


id: GO:1903859
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of dendrite extension.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:PARL","GOC:pad","PMID:24898855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell growth","termid":"GO:0001558"},{"relation_name":"is_a","term_name":"regulation of cell morphogenesis","termid":"GO:0022604"},{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"regulates","term_name":"dendrite extension","termid":"GO:0097484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of dendrite extension","termid":"GO:1903859"}


id: GO:0010385
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to double-stranded methylated DNA. Methylation of cytosine or adenine in DNA is an important mechanism for establishing stable heritable epigenetic marks.","definition_xrefs":["PMID:17242155","GOC:imk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"double-stranded DNA binding","termid":"GO:0003690"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003677"],"is_obsolete":false,"name":"double-stranded methylated DNA binding","termid":"GO:0010385"}


id: SO:0001605
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant within a CDS resulting in the gain of an amino acid to the resulting polypeptide.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_sequence_variant","termid":"SO:0001603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino_acid_insertion","synonyms":[{"name":"amino acid insertion","type":"exact"}],"termid":"SO:0001605"}


id: PBO:0031205
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_during_cellular_response_to_osmotic_stress","termid":"PBO:0031205"}


id: PBO:0062820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"organic solute carrier partner 1","termid":"PBO:0062820"}


id: GO:1901245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a B cell receptor (BCR) from the plasma membrane to the inside of the cell, which results in positive regulation of toll-like receptor 9 (TLR9) signaling. For example, internalized BCR signals to recruit TLR9 from multiple small endosomes to large autophagosome-like compartments to enhance TLR9 signaling.","definition_xrefs":["GOC:TermGenie","PMID:18513998","GOC:amm","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of toll-like receptor 9 signaling pathway","termid":"GO:0034165"},{"relation_name":"is_a","term_name":"B cell receptor internalization","termid":"GO:0036300"},{"relation_name":"is_a","term_name":"positive regulation of signal transduction by receptor internalization","termid":"GO:0038010"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0023052","GO:0016192"],"is_obsolete":false,"name":"positive regulation of toll-like receptor 9 signaling pathway by B cell receptor internalization","synonyms":[{"name":"BCR-induced TLR9 recruitment","type":"narrow"},{"name":"positive regulation of TLR9 signaling pathway by B cell receptor internalization","type":"exact"},{"name":"positive regulation of TLR9 signaling pathway by BCR endocytosis","type":"exact"},{"name":"positive regulation of TLR9 signaling pathway by BCR receptor internalization","type":"exact"},{"name":"positive regulation of toll-like receptor 9 signaling pathway by BCR endocytosis","type":"exact"},{"name":"positive regulation of toll-like receptor 9 signaling pathway by BCR receptor internalization","type":"exact"},{"name":"positive regulation of toll-like receptor 9 signalling pathway by B cell receptor internalization","type":"exact"},{"name":"positive regulation of toll-like receptor 9 signalling pathway by BCR endocytosis","type":"exact"},{"name":"positive regulation of toll-like receptor 9 signalling pathway by BCR receptor internalization","type":"exact"}],"termid":"GO:1901245"}


id: PBO:0000757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human WDR55 family, involved in ribosome biogenesis (predicted)","termid":"PBO:0000757"}


id: MONDO:0015420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cleft lip and alveolus is a fissure type embryopathy that involves the upper lip, nasal base and alveolar ridge in variable degrees.","definition_xrefs":["Orphanet:141291"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orofacial cleft","termid":"MONDO:0000358"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleft lip and alveolus","secondary_identifiers":["SCTID:373643003","UMLS:C1298692","icd11.foundation:1653169553","MEDGEN:720590","GARD:16976","ICD9:525.8"],"termid":"MONDO:0015420","xrefs":{"Monarch":{"xref_id":"0015420"}}}


id: CHEBI:32599
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"A magnesium salt having sulfate as the counterion.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"magnesium sulfate","termid":"CHEBI:32599"}


id: GO:0048341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the paraxial mesoderm. This process pertains to the initial formation of the structure from unspecified parts.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesoderm formation","termid":"GO:0001707"},{"relation_name":"part_of","term_name":"paraxial mesoderm morphogenesis","termid":"GO:0048340"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"paraxial mesoderm formation","secondary_identifiers":["Reactome:R-HSA-9793380"],"termid":"GO:0048341"}


id: PBO:0052698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 16 pseudogene 6","termid":"PBO:0052698"}


id: PBO:0005123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone lysine methyltransferase Set1","termid":"PBO:0005123"}


id: PBO:0067472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 602, pseudogene","termid":"PBO:0067472"}


id: MONDO:0010024
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Short rib-polydactyly syndrome (SRPS), Beemer-Langer type is an extremely rare type of SRPS developing prenatally or immediately after birth and characterized by short and narrow thorax with horizontally oriented ribs. Other bone features include small iliac bones, short tubular bones, bowing of long bones and rarely pre- and post-axial polydactyly. Brain defects are common and some cases of cleft lip, absent internal genitalia and renal, biliary and pancreatic cysts have been reported. The course is rapidly fatal.","definition_xrefs":["Orphanet:93268"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Jeune syndrome","termid":"MONDO:0018770"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"Beemer-Langer syndrome","secondary_identifiers":["MEDGEN:96578","MESH:C537599","OMIM:269860","UMLS:C0432198","DOID:9249","SCTID:254052001","GARD:4832","ICD9:756.9"],"synonyms":[{"name":"Beemer Langer syndrome","type":"related"},{"name":"Beemer-Langer syndrome","type":"exact"},{"name":"SRPS type 4","type":"related"},{"name":"SRTD12","type":"related"},{"name":"Srps 4","type":"related"},{"name":"short rib polydactyly syndrome Beemer-Langer type","type":"related"},{"name":"short rib syndrome, Beemer type","type":"related"},{"name":"short rib-polydactyly syndrome Beemer type","type":"related"},{"name":"short rib-polydactyly syndrome type 4","type":"exact"},{"name":"short rib-polydactyly syndrome type IV","type":"related"},{"name":"short rib-polydactyly syndrome, Beemer-Langer type","type":"related"},{"name":"short rib-polydactyly syndrome, type 4","type":"related"},{"name":"short-rib thoracic dysplasia 12","type":"related"},{"name":"type IV short rib polydactyly syndrome","type":"exact"}],"termid":"MONDO:0010024","xrefs":{"Monarch":{"xref_id":"0010024"}}}


id: PBO:0076323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synergin gamma","termid":"PBO:0076323"}


id: PBO:0091414
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human XPO1","termid":"PBO:0091414"}


id: PBO:0001085
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.4.2","termid":"PBO:0001085"}


id: PBO:0030546
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_cAMP_level","termid":"PBO:0030546"}


id: PATO:0001907
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A surface feature shape quality inhering in a bearer by virtue of the bearer's being like the surface of a compact mass of grapes.","definition_xrefs":["PATOC:cvs"],"direct_ancestors":[{"relation_name":"is_a","term_name":"surface feature shape","termid":"PATO:0001925"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"botryoidal","termid":"PATO:0001907"}


id: MONDO:0002755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A localized, clonal (malignant) plasma cell infiltrate in the bone, without peripheral blood involvement. The most commonly affected bones are the vertebrae, ribs, skull, pelvis and femur. X-rays examination reveals a solitary lytic lesion.","definition_xrefs":["NCIT:C7812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasmacytoma","termid":"MONDO:0005615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"solitary osseous plasmacytoma","secondary_identifiers":["UMLS:C0272256","SCTID:426336007","ICD9:238.6","DOID:3722","ONCOTREE:SPB","MEDGEN:75777"],"synonyms":[{"name":"SPB","type":"related"},{"name":"isolated osseous plasmacytoma","type":"exact"},{"name":"isolated plasmacytoma of bone","type":"exact"},{"name":"solitary plasmacytoma of bone","type":"exact"}],"termid":"MONDO:0002755","xrefs":{"Monarch":{"xref_id":"0002755"}}}


id: GO:0007093
data:
  {"annotated_genes":["SJAG_01082","SJAG_03720","SJAG_01330","SJAG_00071","SJAG_02771","SJAG_04999","SJAG_01677","SJAG_04597","SJAG_01084","SJAG_01605","SJAG_02336","SJAG_01297","SJAG_03529","SJAG_03942","SJAG_03695","SJAG_02563","SJAG_04126","SJAG_01076","SJAG_03681","SJAG_00486","SJAG_01146","SJAG_00169","SJAG_01680","SJAG_03353","SJAG_01010","SJAG_03160","SJAG_00883","SJAG_02098","SJAG_01837","SJAG_01210","SJAG_02026","SJAG_03927","SJAG_01044","SJAG_02074","SJAG_02169","SJAG_01855","SJAG_01873","SJAG_04699","SJAG_02576","SJAG_00327","SJAG_04287","SJAG_02392","SJAG_03602","SJAG_04884","SJAG_03126","SJAG_01679","SJAG_05373","SJAG_02451","SJAG_04280","SJAG_03898","SJAG_00640","SJAG_04671","SJAG_03073","SJAG_00429","SJAG_01429","SJAG_01205","SJAG_00623","SJAG_01401","SJAG_04140","SJAG_01708","SJAG_00364","SJAG_04332","SJAG_04259","SJAG_03048","SJAG_00082","SJAG_02266","SJAG_03026"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112267,99914,91062,107546,116200,104210,108567,114572,114085],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[100860,90336,94745,101757,116304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044878"},{"annotations":[93908,116532,78351,114770,80354,111507,116305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044773"},{"annotations":[79825,100861,94302,117401,71471,99683,109628,117573,117100,79166,112342,99516,72793,116360,91770,75104,106935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033314"},{"annotations":[109203,101939,116202,102675,89284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031568"},{"annotations":[109980,91647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[98754,116306,96183,94876],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031569"},{"annotations":[112038,117315,89461,118010,79767,99685,92133,109629,91771,106936,72791,90551,101371,100862,75598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007095"},{"annotations":[79772,116362,79164,89462,106937,99686,91772,90786,79540,101181,107979,112343,96344,89507,112039,102676,94877,74254,74778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031573"},{"annotations":[115857,99758,110216,102116,106638,114802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[94537],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[116973],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090267"}]},"cv_name":"biological_process","definition":"A signaling process that ensures accurate chromosome replication and segregation by preventing progression through a mitotic cell cycle until conditions are suitable for the cell to proceed to the next stage.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle checkpoint signaling","termid":"GO:0000075"},{"relation_name":"is_a","term_name":"negative regulation of mitotic cell cycle","termid":"GO:0045930"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"}],"gene_count":67,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00082":null,"SJAG_00169":null,"SJAG_00327":null,"SJAG_00364":null,"SJAG_00429":null,"SJAG_00486":null,"SJAG_00623":null,"SJAG_00640":null,"SJAG_00883":null,"SJAG_01010":null,"SJAG_01044":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01146":null,"SJAG_01205":null,"SJAG_01210":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01401":null,"SJAG_01429":null,"SJAG_01605":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01708":null,"SJAG_01837":null,"SJAG_01855":null,"SJAG_01873":null,"SJAG_02026":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02169":null,"SJAG_02266":null,"SJAG_02336":null,"SJAG_02392":null,"SJAG_02451":null,"SJAG_02563":null,"SJAG_02576":null,"SJAG_02771":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03073":null,"SJAG_03126":null,"SJAG_03160":null,"SJAG_03353":null,"SJAG_03529":null,"SJAG_03602":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03720":null,"SJAG_03898":null,"SJAG_03927":null,"SJAG_03942":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04332":null,"SJAG_04597":null,"SJAG_04671":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04999":null,"SJAG_05373":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"mitotic cell cycle checkpoint signaling","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0071780","GO:0072413","GO:0072474","GO:0072456","GO:0031575"],"synonyms":[{"name":"mitotic cell cycle checkpoint","type":"exact"},{"name":"mitotic checkpoint","type":"related"},{"name":"signal transduction involved in mitotic G2/M transition checkpoint","type":"narrow"},{"name":"signal transduction involved in mitotic cell cycle G1/S checkpoint","type":"narrow"},{"name":"signal transduction involved in mitotic cell cycle checkpoint","type":"exact"}],"termid":"GO:0007093","terms_by_termid":{"GO:0007094":null,"GO:0007095":null,"GO:0031568":null,"GO:0031569":null,"GO:0031571":null,"GO:0031573":null,"GO:0033314":null,"GO:0044773":null,"GO:0044878":null,"GO:0090267":null,"GO:0140499":null,"GO:1902426":null}}


id: PBO:0072170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15 pseudogene 7","termid":"PBO:0072170"}


id: GO:1903173
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving fatty alcohol.","definition_xrefs":["PMID:24036493","GOC:TermGenie","GOC:mengo_curators","GO_REF:0000068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol metabolic process","termid":"GO:0006066"},{"relation_name":"is_a","term_name":"fatty acid derivative metabolic process","termid":"GO:1901568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"fatty alcohol metabolic process","synonyms":[{"name":"fatty alcohol metabolism","type":"exact"}],"termid":"GO:1903173"}


id: PBO:0057268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 493","termid":"PBO:0057268"}


id: GO:0050385
data:
  {"annotated_genes":["SJAG_05287"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74698],"is_not":false,"summary":null,"term":"GO:0050385"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-ureidoglycolate = glyoxylate + urea.","definition_xrefs":["RHEA:11304","EC:4.3.2.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amidine-lyase activity","termid":"GO:0016842"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05287":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"ureidoglycolate lyase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:UREIDOGLYCOLATE-LYASE-RXN","KEGG_REACTION:R00776"],"synonyms":[{"name":"(S)-ureidoglycolate urea-lyase (glyoxylate-forming)","type":"related"},{"name":"(S)-ureidoglycolate urea-lyase activity","type":"related"},{"name":"ureidoglycolase activity","type":"related"},{"name":"ureidoglycolatase activity","type":"related"},{"name":"ureidoglycolate hydrolase activity","type":"related"}],"termid":"GO:0050385","terms_by_termid":{"GO:0050385":null}}


id: PBO:0031336
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_benomyl","termid":"PBO:0031336"}


id: MONDO:0014045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Cowden disease in which the cause of the disease is a mutation in the SDHD gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Cowden disease","termid":"MONDO:0016063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005093"],"is_obsolete":false,"name":"Cowden syndrome 3","secondary_identifiers":["OMIM:615106"],"synonyms":[{"name":"CWS3","type":"related"},{"name":"Cowden disease caused by mutation in SDHD","type":"exact"},{"name":"Cowden syndrome 3","type":"exact"},{"name":"Cowden syndrome type 3","type":"exact"},{"name":"SDHD Cowden disease","type":"exact"}],"termid":"MONDO:0014045","xrefs":{"Monarch":{"xref_id":"0014045"}}}


id: PBO:0071556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 21","termid":"PBO:0071556"}


id: GO:0097688
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The neurotransmitter-gated ion channel clustering process in which glutamate receptors are localized to distinct domains in the cell membrane.","definition_xrefs":["GOC:krc","PMID:19723286"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter-gated ion channel clustering","termid":"GO:0072578"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"glutamate receptor clustering","synonyms":[{"name":"glutamatergic receptor clustering","type":"exact"}],"termid":"GO:0097688"}


id: GO:0031036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a bipolar filament composed of myosin II molecules.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myosin filament assembly","termid":"GO:0031034"},{"relation_name":"is_a","term_name":"myosin II filament organization","termid":"GO:0031038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0030036","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"myosin II filament assembly","synonyms":[{"name":"myosin II polymerization","type":"related"}],"termid":"GO:0031036"}


id: GO:1902638
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any neural crest cell differentiation that is involved in parathyroid gland development.","definition_xrefs":["PMID:15741317","GOC:TermGenie","GO_REF:0000060","GOC:nhn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural crest cell differentiation","termid":"GO:0014033"},{"relation_name":"part_of","term_name":"parathyroid gland development","termid":"GO:0060017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural crest cell differentiation involved in parathyroid gland development","termid":"GO:1902638"}


id: PBO:0090834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane thiamine/proton high affinity transmembrane transporter Thi9","termid":"PBO:0090834"}


id: PBO:0045408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPPA3 pseudogene 10","termid":"PBO:0045408"}


id: GO:0097316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an N-acetyl-D-glucosamine stimulus.","definition_xrefs":["PMID:21700702","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to N-acetyl-D-glucosamine","termid":"GO:0097315"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to N-acetyl-D-glucosamine","termid":"GO:0097316"}


id: GO:1903512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving phytanic acid.","definition_xrefs":["PMID:16799769","GO_REF:0000068","GOC:dph","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid metabolic process","termid":"GO:0001676"},{"relation_name":"is_a","term_name":"methyl-branched fatty acid metabolic process","termid":"GO:0097089"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"phytanic acid metabolic process","synonyms":[{"name":"phytanic acid metabolism","type":"exact"}],"termid":"GO:1903512"}


id: PBO:0039526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD33B pseudogene 7","termid":"PBO:0039526"}


id: PBO:0002434
data:
  {"annotation_feature_type":"gene","cv_name":"pathway","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"links stress-activated MAPK (Sty1) pathway to cAMP-dependent protein kinase (Pka1) pathway","termid":"PBO:0002434"}


id: MONDO:0045036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A characteristic of an infectious disease in which the disease affects an immunologically normal host.","direct_ancestors":[{"relation_name":"is_a","term_name":"infectious disease characteristic","termid":"MONDO:0045034"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary infectious","termid":"MONDO:0045036","xrefs":{"Monarch":{"xref_id":"0045036"}}}


id: GO:0034466
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a chromaffin granule.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule lumen","termid":"GO:0034774"},{"relation_name":"part_of","term_name":"chromaffin granule","termid":"GO:0042583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"chromaffin granule lumen","termid":"GO:0034466"}


id: MONDO:0016871
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"},{"relation_name":"is_a","term_name":"chromosome 6 disorder","termid":"MONDO:0700013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of chromosome 6","secondary_identifiers":["MEDGEN:1826013","Orphanet:261791","UMLS:C5679654","GARD:20794"],"synonyms":[{"name":"partial deletion of chromosome type 6","type":"exact"},{"name":"partial monosomy of chromosome 6","type":"exact"}],"termid":"MONDO:0016871","xrefs":{"Monarch":{"xref_id":"0016871"}}}


id: MONDO:0019792
data:
  {"annotated_genes":["SJAG_00686","SJAG_00421","SJAG_02885","SJAG_01356","SJAG_01179","SJAG_02119","SJAG_02377","SJAG_02196","SJAG_01317","SJAG_00526"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011397"},{"annotations":[86522],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013886"},{"annotations":[87455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958231"},{"annotations":[85600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011439"},{"annotations":[86114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011781"},{"annotations":[87616],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008458"},{"annotations":[85538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012450"},{"annotations":[85998,85999],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007574"},{"annotations":[86193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013594"}]},"cv_name":"mondo","definition":"Autosomal dominant cerebellar ataxia (ADCA) type I is a group of spinocerebellar ataxias (SCAs) characterized by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement.","definition_xrefs":["Orphanet:94145"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia","termid":"MONDO:0020380"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00421":null,"SJAG_00526":null,"SJAG_00686":null,"SJAG_01179":null,"SJAG_01317":null,"SJAG_01356":null,"SJAG_02119":null,"SJAG_02196":null,"SJAG_02377":null,"SJAG_02885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0000426","MONDO:0005559"],"is_obsolete":false,"name":"autosomal dominant cerebellar ataxia type I","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5680259","GARD:19252","MEDGEN:1842696"],"synonyms":[{"name":"ADCA1","type":"exact"},{"name":"ADCAI","type":"exact"},{"name":"autosomal dominant cerebellar ataxia type 1","type":"exact"},{"name":"cerebellar plus syndrome","type":"exact"}],"termid":"MONDO:0019792","terms_by_termid":{"MONDO:0007574":null,"MONDO:0008458":null,"MONDO:0011397":null,"MONDO:0011439":null,"MONDO:0011781":null,"MONDO:0012450":null,"MONDO:0013594":null,"MONDO:0013886":null,"MONDO:0958231":null},"xrefs":{"Monarch":{"xref_id":"0019792"}}}


id: GO:0030959
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of two peptidyl-tyrosines to form a 3'-(3'-L-tyrosinyl)-L-tyrosine protein cross-link.","definition_xrefs":["RESID:AA0367"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via 3'-(3'-L-tyrosinyl)-L-tyrosine (obsolete GO:0030959)","termid":"GO:0030959"}


id: PBO:0061109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family pyrin domain containing 2","termid":"PBO:0061109"}


id: GO:0010339
data:
  {"annotated_genes":["SJAG_00239","SJAG_04720","SJAG_01975","SJAG_04723","SJAG_01755","SJAG_04864"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89031],"is_not":false,"summary":null,"term":"GO:0010339"},{"annotations":[103287,116861,103035,103286,107174],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070263"}]},"cv_name":"cellular_component","definition":"The side of the cell wall that is opposite to the side that faces the cell and its contents.","definition_xrefs":["GOC:tb","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cell wall","termid":"GO:0005618"},{"relation_name":"part_of","term_name":"cell surface","termid":"GO:0009986"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00239":null,"SJAG_01755":null,"SJAG_01975":null,"SJAG_04720":null,"SJAG_04723":null,"SJAG_04864":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005618"},{"rel_name":"part_of","termid":"GO:0009986"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0009986","GO:0005575","GO:0005618"],"is_obsolete":false,"name":"external side of cell wall","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010339","terms_by_termid":{"GO:0010339":null,"GO:0070263":null}}


id: PBO:0109647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taxilin gamma Y-linked (pseudogene)","termid":"PBO:0109647"}


id: GO:0051308
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which paired chromosomes are physically detached from each other during male meiosis.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male meiosis chromosome segregation","termid":"GO:0007060"},{"relation_name":"is_a","term_name":"meiotic chromosome separation","termid":"GO:0051307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0008150","GO:0140013","GO:0007049"],"is_obsolete":false,"name":"male meiosis chromosome separation","synonyms":[{"name":"chromosome separation during male meiosis","type":"exact"},{"name":"male meiosis chromosome resolution","type":"exact"}],"termid":"GO:0051308"}


id: PBO:0017952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex substrate recognition subunit Apc10","termid":"PBO:0017952"}


id: FYPO:0003570
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the attachment of spindle microtubules to the kinetochore during a mitotic or meiotic nuclear division is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype","termid":"FYPO:0000145"},{"relation_name":"is_a","term_name":"normal cell cycle process","termid":"FYPO:0006915"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal attachment of spindle microtubules to kinetochore","termid":"FYPO:0003570"}


id: FYPO:0004588
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitosis takes place abnormally after the cell has undergone a normal mitotic nuclear division and passed through the subsequent mitotic interphase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitosis","termid":"FYPO:0000337"},{"relation_name":"is_a","term_name":"abnormal vegetative cell phenotype following normal mitosis","termid":"FYPO:0004593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000337","FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal mitosis following normal mitosis","synonyms":[{"name":"abnormal mitosis following normal mitosis and interphase","type":"exact"},{"name":"abnormal mitosis following normal mitosis and passage through mitotic G1 phase","type":"exact"},{"name":"abnormal mitosis following normal mitosis during vegetative growth","type":"exact"},{"name":"abnormal mitotic nuclear division following normal mitotic nuclear division","type":"exact"},{"name":"abnormal nuclear division following normal nuclear division during mitotic cell cycle","type":"exact"}],"termid":"FYPO:0004588"}


id: PBO:0040933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein 3 pseudogene 4","termid":"PBO:0040933"}


id: MONDO:0001995
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that arises from the mucosal epithelial surface of the sphenoid sinus. Patients may present with nasal fullness, obstruction, and/or epistaxis.","definition_xrefs":["NCIT:C6066"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sphenoidal sinus cancer","termid":"MONDO:0001994"},{"relation_name":"is_a","term_name":"paranasal sinus squamous cell carcinoma","termid":"MONDO:0044705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"sphenoid sinus squamous cell carcinoma","secondary_identifiers":["MEDGEN:234802","UMLS:C1336039","DOID:14547","SCTID:707355002"],"synonyms":[{"name":"epidermoid carcinoma of sphenoid sinus","type":"exact"},{"name":"epidermoid carcinoma of sphenoidal sinus","type":"exact"},{"name":"epidermoid carcinoma of the sphenoid sinus","type":"exact"},{"name":"epidermoid carcinoma of the sphenoidal sinus","type":"exact"},{"name":"sphenoid sinus epidermoid carcinoma","type":"exact"},{"name":"sphenoid sinus squamous cell carcinoma","type":"exact"},{"name":"sphenoidal sinus epidermoid carcinoma","type":"exact"},{"name":"sphenoidal sinus squamous cell carcinoma","type":"exact"},{"name":"squamous cell carcinoma of sphenoid sinus","type":"exact"},{"name":"squamous cell carcinoma of sphenoidal sinus","type":"exact"},{"name":"squamous cell carcinoma of the sphenoid sinus","type":"exact"},{"name":"squamous cell carcinoma of the sphenoidal sinus","type":"exact"}],"termid":"MONDO:0001995","xrefs":{"Monarch":{"xref_id":"0001995"}}}


id: GO:0031638
data:
  {"annotated_genes":["SJAG_02432","SJAG_04785","SJAG_01868"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87818,92160,97964],"is_not":false,"summary":null,"term":"GO:0031638"}]},"cv_name":"biological_process","definition":"The proteolytic processing of an inactive enzyme to an active form.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein processing","termid":"GO:0016485"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01868":null,"SJAG_02432":null,"SJAG_04785":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0051604"],"is_obsolete":false,"name":"zymogen activation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"zymogen activation by proteolytic cleavage","type":"exact"}],"termid":"GO:0031638","terms_by_termid":{"GO:0031638":null}}


id: GO:0046247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of terpenes, any of a large group of hydrocarbons made up of isoprene units.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid catabolic process","termid":"GO:0008300"},{"relation_name":"is_a","term_name":"terpene metabolic process","termid":"GO:0042214"},{"relation_name":"is_a","term_name":"hydrocarbon catabolic process","termid":"GO:0120253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"terpene catabolic process","synonyms":[{"name":"terpene breakdown","type":"exact"},{"name":"terpene catabolism","type":"exact"},{"name":"terpene degradation","type":"exact"}],"termid":"GO:0046247"}


id: PBO:0076175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 1D member 1, pseudogene","termid":"PBO:0076175"}


id: FYECO:0000168
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells are initially grown at a high temperature. This is followed by a heat shock where the temperature is increased to a higher temperature, followed by recovery at the initial temperature.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping heat shock","termid":"FYECO:0000116"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock and recovery at high temperature","synonyms":[{"name":"heat shock for 20-30 min at 48 degrees C, preceeded and followed by growth at high temperature","type":"narrow"}],"termid":"FYECO:0000168"}


id: PBO:0055214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2640","termid":"PBO:0055214"}


id: GO:0004146
data:
  {"annotated_genes":["SJAG_01198"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71344],"is_not":false,"summary":null,"term":"GO:0004146"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,6,7,8-tetrahydrofolate + NADP+ = 7,8-dihydrofolate + NADPH + H+.","definition_xrefs":["EC:1.5.1.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01198":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"dihydrofolate reductase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:DIHYDROFOLATEREDUCT-RXN","Reactome:R-HSA-1497794","RHEA:15009"],"synonyms":[{"name":"5,6,7,8-tetrahydrofolate:NADP+ oxidoreductase activity","type":"related"},{"name":"7,8-dihydrofolate reductase activity","type":"related"},{"name":"DHFR","type":"related"},{"name":"NADPH-dihydrofolate reductase activity","type":"related"},{"name":"dihydrofolate reductase:thymidylate synthase activity","type":"related"},{"name":"dihydrofolate reduction","type":"exact"},{"name":"dihydrofolic acid reductase activity","type":"related"},{"name":"dihydrofolic reductase activity","type":"related"},{"name":"folic acid reductase activity","type":"related"},{"name":"folic reductase activity","type":"related"},{"name":"pteridine reductase:dihydrofolate reductase activity","type":"related"},{"name":"tetrahydrofolate dehydrogenase activity","type":"related"},{"name":"thymidylate synthetase-dihydrofolate reductase activity","type":"related"}],"termid":"GO:0004146","terms_by_termid":{"GO:0004146":null}}


id: MOD:01436
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to cyclo[(prolylserin)-O-yl] cysteinate.","definition_xrefs":["RESID:AA0489#CYS","PubMed:7961166"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclo[(prolylserin)-O-yl] cysteinate","termid":"MOD:01629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"cyclo[(prolylserin)-O-yl] cysteinate (Cys)","synonyms":[{"name":"(3,6-dioxopyrrolo[4,5-a]piperazin-2-yl)methyl cysteinate","type":"exact"},{"name":"MOD_RES Cyclo[(prolylserin)-O-yl] cysteinate","type":"exact"},{"name":"[(3S,8aS)-1,4-dioxooctahydropyrrolo[1,2-a]pyrazin-3-yl]methyl (2R)-2-amino-3-sulfanylpropanoate","type":"exact"},{"name":"cyclo[(prolylserin)-O-yl] cysteinate","type":"exact"}],"termid":"MOD:01436"}


id: MONDO:0001037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"corneal ulcer","termid":"MONDO:0004577"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"ring corneal ulcer","secondary_identifiers":["SCTID:111520007","MEDGEN:509766","DOID:10444","ICD9:370.02","UMLS:C0155068","icd11.foundation:1877531217"],"termid":"MONDO:0001037","xrefs":{"Monarch":{"xref_id":"0001037"}}}


id: PBO:0040416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V0 subunit c pseudogene 1","termid":"PBO:0040416"}


id: MONDO:0021128
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An characteristic of a disease in which the disease is manifested as an isolated feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic or isolated","termid":"MONDO:0021126"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has an isolated presentation","termid":"MONDO:0021128","xrefs":{"Monarch":{"xref_id":"0021128"}}}


id: PATO:0001725
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A male receptivity which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"male receptivity","termid":"PATO:0001721"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased male receptivity","synonyms":[{"name":"high male receptivity","type":"exact"}],"termid":"PATO:0001725"}


id: PBO:0031465
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_nigericin","termid":"PBO:0031465"}


id: MONDO:0005135
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A successful invasion of a host by an organism that uses the host for food and shelter.","definition_xrefs":["NCIT:C27864"],"direct_ancestors":[{"relation_name":"is_a","term_name":"infectious disease","termid":"MONDO:0005550"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parasitic infectious disease","secondary_identifiers":["UMLS:C0030499","DOID:1398","ICD9:134.9","ICD9:136.9","MESH:D010272","ICD9:129","EFO:0001067","ICD9:136.8","MEDGEN:45325","SCTID:17322007","ICD9:134.8","ICD9:376.13","ICD9:136.4","ICD9:360.13"],"synonyms":[{"name":"disease caused by parasite","type":"exact"},{"name":"disease, parasitic","type":"related"},{"name":"diseases, parasitic","type":"related"},{"name":"ectoparasitic disease","type":"narrow"},{"name":"infestation","type":"related"},{"name":"parasite infestation","type":"related"},{"name":"parasitemia","type":"narrow"},{"name":"parasitic disease","type":"exact"},{"name":"parasitic infection","type":"exact"},{"name":"parasitic infectious disease","type":"exact"},{"name":"parasitism","type":"related"},{"name":"parasitosis","type":"related"}],"termid":"MONDO:0005135","xrefs":{"Monarch":{"xref_id":"0005135"}}}


id: GO:0046223
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of aflatoxin, a fungal metabolite found as a contaminant in moldy grains that induces liver cancer. Aflatoxin induces a G to T transversion at codon 249 of p53, leading to its inactivation. Aflatoxin is converted to a chemical carcinogen by P450.","definition_xrefs":["PMID:20807200","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mycotoxin catabolic process","termid":"GO:0043387"},{"relation_name":"is_a","term_name":"aflatoxin metabolic process","termid":"GO:0046222"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0098754","GO:0019748"],"is_obsolete":false,"name":"aflatoxin catabolic process","synonyms":[{"name":"aflatoxin breakdown","type":"exact"},{"name":"aflatoxin catabolism","type":"exact"},{"name":"aflatoxin degradation","type":"exact"}],"termid":"GO:0046223"}


id: PBO:0078242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 22-1 (pseudogene)","termid":"PBO:0078242"}


id: PBO:0003323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial metalloendopeptidase (predicted)","termid":"PBO:0003323"}


id: PBO:0030439
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_tRNA_methylation","termid":"PBO:0030439"}


id: MONDO:0016776
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Frontal fibrosing alopecia (FFA) is a rare variant of lichen planopilaris characterized by symmetrical, progressive, band-like anterior hair loss of the scalp.","definition_xrefs":["Orphanet:254492"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia","termid":"MONDO:0004907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frontal fibrosing alopecia","secondary_identifiers":["GARD:10886","SCTID:717055000","icd11.foundation:1257078333","MEDGEN:899012","UMLS:C4255374","ICD10CM:L66.1"],"synonyms":[{"name":"FFA","type":"exact"}],"termid":"MONDO:0016776","xrefs":{"Monarch":{"xref_id":"0016776"}}}


id: GO:0102053
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (-)-jasmonate + L-isoleucine + ATP(4-) = H+ + (-)-jasmonoyl-L-isoleucine + AMP(2-) + diphosphoric acid.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete (-)-jasmonoyl-isoleucine synthetase activity (obsolete GO:0102053)","termid":"GO:0102053"}


id: PBO:0056635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 13L","termid":"PBO:0056635"}


id: GO:1900053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of retinoic acid biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hormone metabolic process","termid":"GO:0032351"},{"relation_name":"is_a","term_name":"negative regulation of isoprenoid metabolic process","termid":"GO:0045827"},{"relation_name":"is_a","term_name":"negative regulation of vitamin metabolic process","termid":"GO:0046137"},{"relation_name":"is_a","term_name":"negative regulation of lipid biosynthetic process","termid":"GO:0051055"},{"relation_name":"is_a","term_name":"regulation of retinoic acid biosynthetic process","termid":"GO:1900052"},{"relation_name":"negatively_regulates","term_name":"retinoic acid biosynthetic process","termid":"GO:0002138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006766"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006766"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006766","GO:0006629"],"is_obsolete":false,"name":"negative regulation of retinoic acid biosynthetic process","synonyms":[{"name":"down regulation of retinoic acid anabolic process","type":"exact"},{"name":"down regulation of retinoic acid biosynthetic process","type":"related"},{"name":"down-regulation of retinoic acid anabolic process","type":"exact"},{"name":"down-regulation of retinoic acid biosynthetic process","type":"related"},{"name":"downregulation of retinoic acid anabolic process","type":"exact"},{"name":"downregulation of retinoic acid biosynthetic process","type":"related"},{"name":"inhibition of retinoic acid anabolic process","type":"exact"},{"name":"inhibition of retinoic acid biosynthetic process","type":"related"},{"name":"negative regulation of retinoic acid anabolic process","type":"exact"}],"termid":"GO:1900053"}


id: MONDO:0015204
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microlissencephaly describes a heterogenous group of a rare cortical malformations characterized by lissencephaly in combination with severe congenital microcephaly, presenting with spasticity, severe developmental delay, and seizures and with survival varying from days to years.","definition_xrefs":["Orphanet:1083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lissencephaly spectrum disorders","termid":"MONDO:0018838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"microlissencephaly","secondary_identifiers":["DOID:0112234","icd11.foundation:169315445","UMLS:C1956147","MEDGEN:365439","GARD:16555"],"termid":"MONDO:0015204","xrefs":{"Monarch":{"xref_id":"0015204"}}}


id: GO:0060410
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of the chemical reactions and pathways involving acetylcholine, the acetic acid ester of the organic base choline. Acetylcholine is a major neurotransmitter and neuromodulator both in the central and peripheral nervous systems. It also acts as a paracrine signal in various non-neural tissues.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of amine metabolic process","termid":"GO:0033239"},{"relation_name":"is_a","term_name":"regulation of acetylcholine metabolic process","termid":"GO:0060408"},{"relation_name":"negatively_regulates","term_name":"acetylcholine metabolic process","termid":"GO:0008291"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of acetylcholine metabolic process","termid":"GO:0060410"}


id: GO:0045822
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of heart contraction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart contraction","termid":"GO:0008016"},{"relation_name":"is_a","term_name":"negative regulation of blood circulation","termid":"GO:1903523"},{"relation_name":"negatively_regulates","term_name":"heart contraction","termid":"GO:0060047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of heart contraction","synonyms":[{"name":"down regulation of heart contraction","type":"exact"},{"name":"down-regulation of heart contraction","type":"exact"},{"name":"downregulation of heart contraction","type":"exact"},{"name":"inhibition of heart contraction","type":"narrow"},{"name":"negative regulation of cardiac contraction","type":"related"}],"termid":"GO:0045822"}


id: MONDO:0018035
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndrome with combined immunodeficiency (obsolete MONDO:0018035)","secondary_identifiers":["NANDO:2100203","Orphanet:331217"],"termid":"MONDO:0018035","xrefs":{"Monarch":{"xref_id":"0018035"}}}


id: MONDO:0013043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"atypical hemolytic uremic syndrome with complement gene abnormality","termid":"MONDO:0035290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"atypical hemolytic-uremic syndrome with C3 anomaly","secondary_identifiers":["MEDGEN:442875","OMIM:612925","GARD:18555","Orphanet:93575","UMLS:C2752037"],"synonyms":[{"name":"AHUS5","type":"related"},{"name":"Ahus, susceptibility to, 5","type":"related"},{"name":"D-HUS with C3 anomaly","type":"exact"},{"name":"aHUS with C3 anomaly","type":"exact"},{"name":"atypical HUS with C3 anomaly","type":"exact"},{"name":"hemolytic uremic syndrome with DGKE deficiency","type":"exact"},{"name":"hemolytic uremic syndrome, atypical, susceptibility to, 5","type":"related"},{"name":"hemolytic uremic syndrome, atypical, susceptibility to, type 5","type":"exact"},{"name":"hemolytic-uremic syndrome without diarrhea with C3 anomaly","type":"exact"},{"name":"hemolytic-uremic syndrome without diarrhoea with C3 anomaly","type":"exact"},{"name":"susceptibility to atypical hemolytic uremic syndrome 5","type":"related"}],"termid":"MONDO:0013043","xrefs":{"Monarch":{"xref_id":"0013043"}}}


id: PBO:0063862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piezo type mechanosensitive ion channel component 1 pseudogene 1","termid":"PBO:0063862"}


id: PBO:0082475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cAMP-dependent protein kinase catalytic subunit; promotes vegetative growth in response to nutrients via the Ras-cAMP signaling pathway; partially redundant with Tpk1p and Tpk3p; localizes to P-bodies during stationary phase; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082475"}


id: MONDO:0032780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities","secondary_identifiers":["UMLS:C5193124","OMIM:618493","MEDGEN:1672905","Orphanet:656273"],"synonyms":[{"name":"HIDEA","type":"related"},{"name":"HYPOTONIA, HYPOVENTILATION, IMPAIRED INTELLECTUAL DEVELOPMENT, DYSAUTONOMIA, EPILEPSY, AND EYE ABNORMALITIES","type":"related"}],"termid":"MONDO:0032780","xrefs":{"Monarch":{"xref_id":"0032780"}}}


id: MONDO:0006735
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retrograde flow of duodenal contents (bile acids; pancreatic juice) into the stomach.","definition_xrefs":["MESH:D004383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"duodenal disorder","termid":"MONDO:0002866"},{"relation_name":"is_a","term_name":"gastroesophageal reflux disease","termid":"MONDO:0007186"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"duodenogastric reflux","secondary_identifiers":["MEDGEN:4420","MedDRA:10060865","EFO:1000909","DOID:4071","UMLS:C0013299"],"synonyms":[{"name":"duodenogastric reflux (finding)","type":"exact"}],"termid":"MONDO:0006735","xrefs":{"Monarch":{"xref_id":"0006735"}}}


id: PBO:0028800
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_chromatin_binding_at_mating-type_region_replication_fork_barrier","termid":"PBO:0028800"}


id: GO:0070168
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of biomineral tissue development, the formation of hard tissues that consist mainly of inorganic compounds.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of biomineral tissue development","termid":"GO:0070167"},{"relation_name":"negatively_regulates","term_name":"biomineral tissue development","termid":"GO:0031214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of biomineral tissue development","termid":"GO:0070168"}


id: PBO:0014298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S. pombe specific family","termid":"PBO:0014298"}


id: GO:0005230
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of an ion by a channel that opens when a specific extracellular ligand has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligand-gated monoatomic ion channel activity","termid":"GO:0015276"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"extracellular ligand-gated monoatomic ion channel activity","synonyms":[{"name":"extracellular ligand-gated ion channel activity","type":"broad"}],"termid":"GO:0005230"}


id: GO:0018029
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The palmitoylation of peptidyl-lysine to form peptidyl-N6-palmitoyl-L-lysine.","definition_xrefs":["RESID:AA0077"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-lysine palmitoylation (obsolete GO:0018029)","termid":"GO:0018029"}


id: PBO:0027586
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_meiotic_sister_chromatid_cohesion_at_centromere","termid":"PBO:0027586"}


id: GO:0003067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which hormones modulate the force with which blood passes through the circulatory system contributing to different values of blood pressure oscillating with a regularity of approximately 24 hours. A hormone is one of a group of substances formed in very small amounts in one specialized organ or group of cells and carried (sometimes in the bloodstream) to another organ or group of cells, in the same organism, upon which they have a specific regulatory action.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure by hormone","termid":"GO:0001990"},{"relation_name":"part_of","term_name":"circadian regulation of systemic arterial blood pressure","termid":"GO:0003052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"circadian regulation of systemic arterial blood pressure by hormone","termid":"GO:0003067"}


id: PBO:0034138
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-confers_advantage_in","termid":"PBO:0034138"}


id: PBO:0039041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AGBL carboxypeptidase 3","termid":"PBO:0039041"}


id: MONDO:0011029
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloid tumor suppressor","secondary_identifiers":["UMLS:C1832510","MEDGEN:318644","OMIM:601308"],"synonyms":[{"name":"myeloid leukemia-related locus","type":"related"},{"name":"myeloid tumor suppressor","type":"exact"}],"termid":"MONDO:0011029","xrefs":{"Monarch":{"xref_id":"0011029"}}}


id: FYPO:0005989
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype that affects the localization of a protein in a cell during conjugation with cellular fusion. A protein may be observed in a place where it is not normally found, absent from a place where it is normally found, or both.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization","termid":"FYPO:0001370"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein localization during mating","synonyms":[{"name":"abnormal cellular protein localisation during mating","type":"exact"},{"name":"abnormal cellular protein localization during mating","type":"exact"},{"name":"abnormal protein localisation during mating","type":"exact"},{"name":"abnormal protein localization during conjugation with cellular fusion","type":"exact"}],"termid":"FYPO:0005989"}


id: GO:1903792
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of anion transport.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:11336802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of monoatomic ion transport","termid":"GO:0043271"},{"relation_name":"is_a","term_name":"regulation of monoatomic anion transport","termid":"GO:0044070"},{"relation_name":"negatively_regulates","term_name":"monoatomic anion transport","termid":"GO:0006820"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of monoatomic anion transport","synonyms":[{"name":"down regulation of anion transport","type":"exact"},{"name":"down-regulation of anion transport","type":"exact"},{"name":"downregulation of anion transport","type":"exact"},{"name":"inhibition of anion transport","type":"narrow"},{"name":"negative regulation of anion transport","type":"broad"}],"termid":"GO:1903792"}


id: MONDO:0810000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An eye disorder described by the growth of new blood vessels that originate from the choroid through a break in the Bruch membrane into the sub–retinal pigment epithelium (sub-RPE) or subretinal space. Choroidal neovascularization (CNV) is a major cause of visual loss.","direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"choroidal neovascularization","secondary_identifiers":["MESH:D020256","MEDGEN:154726","UMLS:C0600518","HP:0011506"],"termid":"MONDO:0810000","xrefs":{"Monarch":{"xref_id":"0810000"}}}


id: PBO:0030076
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_arginine_import","termid":"PBO:0030076"}


id: GO:0045216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a cell-cell junction. A cell-cell junction is a specialized region of connection between two cells.","definition_xrefs":["GOC:dph","GOC:ai","GOC:mah","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell junction organization","termid":"GO:0034330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell-cell junction organization","secondary_identifiers":["Reactome:R-HSA-421270"],"synonyms":[{"name":"cell-cell junction assembly and maintenance","type":"exact"},{"name":"cell-cell junction biogenesis","type":"related"},{"name":"cell-cell junction organisation","type":"exact"},{"name":"intercellular junction assembly and maintenance","type":"exact"}],"termid":"GO:0045216"}


id: GO:0060708
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell of the ectoplacental cone acquires specialized features of a spongiotrophoblast of the placenta. A spongiotrophoblast cell is a basophilic cell.","definition_xrefs":["PMID:16269175","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation involved in embryonic placenta development","termid":"GO:0060706"},{"relation_name":"part_of","term_name":"spongiotrophoblast layer development","termid":"GO:0060712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"spongiotrophoblast differentiation","synonyms":[{"name":"spongiotrophoblast cell differentiation","type":"exact"}],"termid":"GO:0060708"}


id: PBO:0044779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DExD/H-box 60 like","termid":"PBO:0044779"}


id: MONDO:0024349
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A prevalent and benign dermatological condition that predominantly affects children and adolescents. The name \\\"pityriasis alba\\\" derives from its appearance, where \\\"pityriasis\\\" denotes the fine scales and \\\"alba\\\" signifies the pale color (hypopigmentation).","definition_xrefs":["PMID:28613715"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exanthem","termid":"MONDO:0006547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"pityriasis alba","secondary_identifiers":["MEDGEN:39322","ICD9:696.5","SCTID:402296004","UMLS:C0085657","icd11.foundation:1386947078"],"termid":"MONDO:0024349","xrefs":{"Monarch":{"xref_id":"0024349"}}}


id: PBO:0039221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldo-keto reductase family 7 member A2","termid":"PBO:0039221"}


id: PBO:0090732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQGAP domain cytoskeleton scaffold protein Rng2","termid":"PBO:0090732"}


id: GO:0097184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an azide stimulus.","definition_xrefs":["PMID:16846222","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to azide","termid":"GO:0097184"}


id: PBO:0075504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis associated serine rich 2","termid":"PBO:0075504"}


id: SO:0000916
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000916 edit_operation (obsolete SO:0000916)","synonyms":[{"name":"edit operation","type":"exact"}],"termid":"SO:0000916"}


id: PBO:0080433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS51 pseudogene 17","termid":"PBO:0080433"}


id: GO:0047236
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: methylazoxymethanol + UDP-D-glucose = H+ + cycasin + UDP.","definition_xrefs":["EC:2.4.1.171","MetaCyc:2.4.1.171-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016757","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"methyl-ONN-azoxymethanol beta-D-glucosyltransferase activity","secondary_identifiers":["RHEA:20205"],"synonyms":[{"name":"UDP-glucose:methyl-ONN-azoxymethanol beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose-methylazoxymethanol glucosyltransferase activity","type":"related"},{"name":"cycasin synthase activity","type":"related"},{"name":"methyl-ONN-azoxymethanol glucosyltransferase activity","type":"exact"},{"name":"uridine diphosphoglucose-methylazoxymethanol glucosyltransferase activity","type":"related"}],"termid":"GO:0047236"}


id: MONDO:0015009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lymphatic malformation","termid":"MONDO:0019313"},{"relation_name":"is_a","term_name":"EPHB4-associated vascular malformation spectrum","termid":"MONDO:0700080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"lymphatic malformation 7","secondary_identifiers":["OMIM:617300","MEDGEN:934596","UMLS:C4310629"],"synonyms":[{"name":"HFASD","type":"exact"},{"name":"hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to","type":"exact"},{"name":"hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to; HFASD","type":"exact"}],"termid":"MONDO:0015009","xrefs":{"Monarch":{"xref_id":"0015009"}}}


id: MONDO:0016775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lichen planus (LP) pemphigoides is a rare cross-over syndrome between lichen planus and bullous pemphigoid.","definition_xrefs":["Orphanet:254478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lichen planus","termid":"MONDO:0006572"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"lichen planus pemphigoides","secondary_identifiers":["UMLS:C0406369","SCTID:238653005","icd11.foundation:1373932539","GARD:12677","MEDGEN:590352"],"synonyms":[{"name":"LP pemphigoides","type":"exact"}],"termid":"MONDO:0016775","xrefs":{"Monarch":{"xref_id":"0016775"}}}


id: MONDO:0019101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinal cavernous hemangioma is a rare, benign, usually unilateral retinal vascular hamartoma that in most cases is asymptomatic but in some patients may present with blurred vision or floaters and that is characterized by the presence of grape-like vacuoles.","definition_xrefs":["Orphanet:71213"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital vitreoretinal dysplasia","termid":"MONDO:0020247"},{"relation_name":"is_a","term_name":"retina neoplasm","termid":"MONDO:0021231"},{"relation_name":"is_a","term_name":"vascular neoplasm","termid":"MONDO:0024296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0002320"],"is_obsolete":false,"name":"retinal capillary malformation","secondary_identifiers":["GARD:18908"],"termid":"MONDO:0019101","xrefs":{"Monarch":{"xref_id":"0019101"}}}


id: PBO:0038530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 4, N-acyl phospholipase B","termid":"PBO:0038530"}


id: MONDO:0006417
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse large B-cell lymphoma that arises from the small intestine.","definition_xrefs":["NCIT:C96055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"small intestine lymphoma","termid":"MONDO:0001852"},{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"small intestinal diffuse large B-cell lymphoma","secondary_identifiers":["EFO:1000534","MEDGEN:474155","UMLS:C3272522"],"synonyms":[{"name":"diffuse large B-cell lymphoma of small intestine","type":"exact"},{"name":"small intestinal diffuse large B-cell lymphoma","type":"exact"},{"name":"small intestine diffuse large B-cell lymphoma","type":"exact"}],"termid":"MONDO:0006417","xrefs":{"Monarch":{"xref_id":"0006417"}}}


id: PATO:0001074
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001074 absolute impulse (obsolete PATO:0001074)","termid":"PATO:0001074"}


id: PR:000027513
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- prz1 gene or a 1:1 ortholog thereof.","definition_xrefs":["PRO:CNA","PMID:12637524"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptional regulator prz1","pombase_gene_id":"SPAC4G8.13c","synonyms":[{"name":"Pbp1-responsive zinc finger protein 1","type":"exact"},{"name":"prz1","type":"exact"}],"termid":"PR:000027513"}


id: MONDO:0003372
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant smooth muscle neoplasm, arising from the vulva. It is characterized by a proliferation of neoplastic spindle cells.","definition_xrefs":["NCIT:C40318"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyosarcoma","termid":"MONDO:0005058"},{"relation_name":"is_a","term_name":"vulva sarcoma","termid":"MONDO:0005214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"vulvar leiomyosarcoma","secondary_identifiers":["DOID:5286","UMLS:C2168304","EFO:1001975","MEDGEN:378348"],"synonyms":[{"name":"leiomyosarcoma of mammalian vulva","type":"exact"},{"name":"mammalian vulva leiomyosarcoma","type":"exact"}],"termid":"MONDO:0003372","xrefs":{"Monarch":{"xref_id":"0003372"}}}


id: GO:0090277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of the regulated release of a peptide hormone from secretory granules.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of peptide secretion","termid":"GO:0002793"},{"relation_name":"is_a","term_name":"positive regulation of hormone secretion","termid":"GO:0046887"},{"relation_name":"is_a","term_name":"regulation of peptide hormone secretion","termid":"GO:0090276"},{"relation_name":"positively_regulates","term_name":"peptide hormone secretion","termid":"GO:0030072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of peptide hormone secretion","termid":"GO:0090277"}


id: GO:0140988
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of ADP from one side of a membrane to the other according to the reaction: ADP(out) + phosphate(in) = ADP(in) + phosphate(out).","definition_xrefs":["PMID:15123600"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ADP transmembrane transporter activity","termid":"GO:0015217"},{"relation_name":"is_a","term_name":"organophosphate:phosphate antiporter activity","termid":"GO:0015315"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"ADP:phosphate antiporter activity","secondary_identifiers":["RHEA:65844"],"synonyms":[{"name":"ADP:inorganic phosphate antiporter activity","type":"exact"},{"name":"inorganic phosphate:ADP antiporter activity","type":"exact"}],"termid":"GO:0140988"}


id: PBO:0060972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear transcription factor Y subunit gamma","termid":"PBO:0060972"}


id: MONDO:0700243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinopathy caused by a variant in the CACNA1F gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"CACNA1F-related retinopathy","synonyms":[{"name":"CACNA1F-related retinopathy","type":"exact"}],"termid":"MONDO:0700243","xrefs":{"Monarch":{"xref_id":"0700243"}}}


id: PBO:0065717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Prader Willi/Angelman region RNA 1","termid":"PBO:0065717"}


id: PBO:0067292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 377, pseudogene","termid":"PBO:0067292"}


id: PBO:0041782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcyphosine","termid":"PBO:0041782"}


id: MONDO:0013727
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any pregnancy loss, recurrent, susceptibility in which the cause of the disease is a mutation in the F5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pregnancy loss, recurrent, susceptibility","termid":"MONDO:0000144"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pregnancy loss, recurrent, susceptibility to, 1","secondary_identifiers":["UMLS:C3280670","OMIM:614389","MEDGEN:482300"],"synonyms":[{"name":"F5 pregnancy loss, recurrent, susceptibility","type":"exact"},{"name":"RPRGL1","type":"related"},{"name":"Rpl","type":"related"},{"name":"Rprgl","type":"related"},{"name":"abortion, spontaneous, recurrent","type":"related"},{"name":"embryonic loss, recurrent","type":"related"},{"name":"fetal loss, recurrent, susceptibility to","type":"related"},{"name":"foetal loss, recurrent, susceptibility to","type":"related"},{"name":"miscarriage, recurrent","type":"related"},{"name":"pregnancy loss, recurrent, susceptibility caused by mutation in F5","type":"exact"},{"name":"pregnancy loss, recurrent, susceptibility to, 1","type":"exact"},{"name":"pregnancy loss, recurrent, susceptibility to, type 1","type":"exact"},{"name":"stillbirth, recurrent","type":"related"}],"termid":"MONDO:0013727","xrefs":{"Monarch":{"xref_id":"0013727"}}}


id: GO:0003132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the transfer of information from mesodermal cells to endodermal cells that contributes to heart induction.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesodermal-endodermal cell signaling","termid":"GO:0003131"},{"relation_name":"part_of","term_name":"heart induction","termid":"GO:0003129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"mesodermal-endodermal cell signaling involved in heart induction","synonyms":[{"name":"mesodermal-endodermal cell signalling involved in heart induction","type":"exact"}],"termid":"GO:0003132"}


id: PBO:0077354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 94","termid":"PBO:0077354"}


id: MONDO:0024327
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Impairment of the renal function due to chronic kidney damage.","definition_xrefs":["NCIT:C9438"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney failure","termid":"MONDO:0001106"},{"relation_name":"is_a","term_name":"chronic kidney disease","termid":"MONDO:0005300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"chronic renal failure syndrome","secondary_identifiers":["MESH:D051436","MEDGEN:9637","NANDO:2100023","SCTID:90688005","ICD9:585.9","UMLS:C0022661"],"synonyms":[{"name":"CRF - chronic renal failure","type":"exact"},{"name":"Chronic renal disease","type":"exact"},{"name":"chronic kidney failure","type":"exact"},{"name":"chronic renal failure","type":"exact"},{"name":"chronic renal failure disease","type":"exact"},{"name":"kidney failure, chronic","type":"exact"}],"termid":"MONDO:0024327","xrefs":{"Monarch":{"xref_id":"0024327"}}}


id: GO:0062181
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catatlysis of the reaction: calcitriol + 2 H+ + O2 + 2 reduced [adrenodoxin] = 1alpha,23S,25-trihydroxycholecalciferol + H2O + 2 oxidized [adrenodoxin].","definition_xrefs":["PMID:22100522","PMID:30205156","RHEA:49192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin D 23-hydroxylase activity","termid":"GO:0062179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"1-alpha,25-dihydroxyvitamin D3 23-hydroxylase activity","termid":"GO:0062181"}


id: GO:0005900
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric receptor for the cytokine oncostatin-M (OSM). In humans the receptor complex is made up of the gene products gp130 and OSMR-beta.","definition_xrefs":["GOC:jl","PMID:8999038"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane signaling receptor complex","termid":"GO:0098802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"oncostatin-M receptor complex","termid":"GO:0005900"}


id: PBO:0054764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2176","termid":"PBO:0054764"}


id: GO:0031702
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1 angiotensin receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angiotensin receptor binding","termid":"GO:0031701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"type 1 angiotensin receptor binding","synonyms":[{"name":"AT1 receptor binding","type":"exact"},{"name":"type 1 angiotensin receptor ligand","type":"narrow"}],"termid":"GO:0031702"}


id: PBO:0064719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 55","termid":"PBO:0064719"}


id: MONDO:0001501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sarcoma involving a retroperitoneal space.","definition_xrefs":["MONDO:patterns/sarcoma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retroperitoneal cancer","termid":"MONDO:0005941"},{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"retroperitoneal sarcoma","secondary_identifiers":["SCTID:307219002","MEDGEN:107937","NCIT:C4832","UMLS:C0585129","DOID:12341"],"synonyms":[{"name":"retroperitoneal sarcoma","type":"exact"},{"name":"retroperitoneal space sarcoma","type":"exact"},{"name":"sarcoma of retroperitoneal space","type":"exact"}],"termid":"MONDO:0001501","xrefs":{"Monarch":{"xref_id":"0001501"}}}


id: PBO:0050451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOATZ cilia and flagella associated protein","termid":"PBO:0050451"}


id: PBO:0059627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MTCH1 pseudogene 2","termid":"PBO:0059627"}


id: MONDO:0034022
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Bethlem myopathy","termid":"MONDO:0008029"},{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"Bethlem myopathy 2","secondary_identifiers":["UMLS:C4225313","GARD:16121","Orphanet:536516","MEDGEN:907426","OMIM:616471"],"synonyms":[{"name":"BTHLM2","type":"exact"},{"name":"Bethlem myopathy 2","type":"exact"},{"name":"Bethlem myopathy caused by mutation in COL12A1","type":"exact"},{"name":"Bethlem myopathy type 2","type":"exact"},{"name":"COL12A1 Bethlem myopathy","type":"exact"},{"name":"EDS, myopathic type","type":"exact"},{"name":"Ehlers-Danlos syndrome, myopathic type","type":"exact"},{"name":"myopathic EDS","type":"exact"},{"name":"myopathic Ehlers-Danlos syndrome","type":"exact"}],"termid":"MONDO:0034022","xrefs":{"Monarch":{"xref_id":"0034022"}}}


id: PBO:0054459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1856","termid":"PBO:0054459"}


id: PBO:0062618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily X member 1","termid":"PBO:0062618"}


id: GO:0140905
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: R-CH + a halogen + H2O2 = R-C-halogen + H2O.","definition_xrefs":["PMID:28466644","PMID:34368824"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxidase activity","termid":"GO:0004601"},{"relation_name":"is_a","term_name":"halogenase activity","termid":"GO:0140906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"haloperoxidase activity","termid":"GO:0140905"}


id: PBO:0040867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bMERB domain containing 1","termid":"PBO:0040867"}


id: PBO:0000966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3 Meu34 (predicted)","termid":"PBO:0000966"}


id: PBO:0076444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 15","termid":"PBO:0076444"}


id: MONDO:0005868
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A laboratory test result indicating an abnormal amount of circulating nucleated red blood cells and immature red blood cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic aplastic anemia","termid":"MONDO:0012197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"myelophthisic anemia","secondary_identifiers":["DOID:2354","SCTID:2694001","NCIT:C36218","ICD9:285.8","UMLS:C0002890","EFO:0007388","MEDGEN:1529","ICD10CM:D61.82","MESH:D000750"],"synonyms":[{"name":"anaemia LEUKOERYTHROBLASTIC","type":"exact"},{"name":"anemia LEUKOERYTHROBLASTIC","type":"exact"},{"name":"anemia, leukoerythroblastic","type":"exact"},{"name":"leukoerythroblastic reaction","type":"exact"},{"name":"leukoerythroblastosis","type":"exact"},{"name":"myelophthisis","type":"related"}],"termid":"MONDO:0005868","xrefs":{"Monarch":{"xref_id":"0005868"}}}


id: PBO:0089677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COPII cargo receptor subunit Sec23a","termid":"PBO:0089677"}


id: MONDO:0017269
data:
  {"annotated_genes":["SJAG_02855"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"}]},"cv_name":"mondo","definition":"X-linked form of inherited ichthyosis syndromic form.","definition_xrefs":["MONDO:patterns/x_linked"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02855":null},"genotype_count":0,"is_obsolete":false,"name":"X-linked ichthyosis syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MedDRA:10048063","Orphanet:281210","GARD:21109"],"synonyms":[{"name":"X-linked inherited ichthyosis syndromic form","type":"exact"},{"name":"inherited ichthyosis syndromic form, X-linked","type":"exact"}],"termid":"MONDO:0017269","terms_by_termid":{"MONDO:0010621":null},"xrefs":{"Monarch":{"xref_id":"0017269"}}}


id: MONDO:0017062
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated spina bifida","termid":"MONDO:0019351"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"spina bifida aperta","secondary_identifiers":["GARD:20951","icd11.foundation:187581000","MEDGEN:181490","UMLS:C0917813","Orphanet:268369","SCTID:58557008"],"termid":"MONDO:0017062","xrefs":{"Monarch":{"xref_id":"0017062"}}}


id: PBO:0004706
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.13.-","termid":"PBO:0004706"}


id: MONDO:0004046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brain meningioma that occurs during childhood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pediatric meningioma","termid":"MONDO:0003057"},{"relation_name":"is_a","term_name":"brain neoplasm","termid":"MONDO:0021211"},{"relation_name":"is_a","term_name":"intracranial meningioma","termid":"MONDO:0850302"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood brain meningioma","secondary_identifiers":["DOID:6939","NCIT:C6253","UMLS:C1332949","MEDGEN:234122"],"synonyms":[{"name":"Brain meningioma","type":"exact"},{"name":"brain paediatric meningioma","type":"exact"},{"name":"brain pediatric meningioma","type":"exact"},{"name":"childhood meningioma of brain","type":"exact"},{"name":"childhood meningioma of the brain","type":"exact"},{"name":"paediatric brain meningioma","type":"exact"},{"name":"paediatric meningioma of brain","type":"exact"},{"name":"paediatric meningioma of the brain","type":"exact"},{"name":"pediatric brain meningioma","type":"exact"},{"name":"pediatric meningioma of brain","type":"exact"},{"name":"pediatric meningioma of the brain","type":"exact"}],"termid":"MONDO:0004046","xrefs":{"Monarch":{"xref_id":"0004046"}}}


id: FYPO:0000647
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An inviable phenotype in which a vegetative cell lyses, i.e. the plasma membrane ruptures and cytoplasm is lost. Note that in fission yeast cell lysis, the integrity of the cell wall is also compromised.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"is_a","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"is_a","term_name":"cell lysis","termid":"FYPO:0002488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"vegetative cell lysis","synonyms":[{"name":"cell lysis during vegetative growth","type":"exact"},{"name":"cytolysis during vegetative growth","type":"exact"},{"name":"inviable, lysed vegetative cell","type":"exact"},{"name":"vegetative cell lysis during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000647"}


id: PBO:0113228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N6-Methyladenosine (m6A) reader; co-transcriptionally recruited to specific methylated mRNAs during meiotic prophase, facilitating protein synthesis and subsequent decay of m6A modified transcripts, resulting in timely meiotic recombination; regulates PHO4 mRNA stability, binding to the 3'UTR in a phosphate-dependent manner; posttranscriptional regulator of phosphate and glucose metabolism; contains a conserved YTH domain with RNA-binding activity; human homolog YTHDF2 complements a null mutant","termid":"PBO:0113228"}


id: MONDO:0015907
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epimetaphyseal skeletal dysplasia","secondary_identifiers":["GARD:2176","Orphanet:1819"],"termid":"MONDO:0015907","xrefs":{"Monarch":{"xref_id":"0015907"}}}


id: GO:1904638
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a resveratrol stimulus.","definition_xrefs":["GO_REF:0000071","PMID:23555824","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stilbenoid","termid":"GO:0035634"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to resveratrol","termid":"GO:1904638"}


id: MONDO:0800114
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polyclonal hyperplasia of bronchiolar associated lymphoid tissue characterized by the development of lymphoid follicles with germinal centers in walls of the small airways.","definition_xrefs":["PMID:32040879"],"direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic interstitial pneumonia","termid":"MONDO:0002429"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"follicular bronchiolits","termid":"MONDO:0800114","xrefs":{"Monarch":{"xref_id":"0800114"}}}


id: MONDO:0016004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aminopterin/Methotrexate embryofetopathy is a syndrome of developmental anomalies characterized by growth deficiency, facial dysmorphism and skull, limb and neural defects secondary to maternal exposure to aminopterin or methotrexate (MTX) during pregnancy.","definition_xrefs":["Orphanet:1908"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxic or drug-related embryofetopathy","termid":"MONDO:0016677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminopterin/methotrexate embryofetopathy","secondary_identifiers":["MEDGEN:98491","SCTID:65986000","MedDRA:10071183","UMLS:C0432367","ICD9:759.89","NCIT:C98928"],"synonyms":[{"name":"aminopterin embryopathy syndrome","type":"exact"},{"name":"aminopterin fetopathy syndrome","type":"related"},{"name":"aminopterin syndrome","type":"related"},{"name":"fetal aminopterin syndrome","type":"exact"},{"name":"fetal methotrexate syndrome","type":"related"},{"name":"foetal aminopterin syndrome","type":"exact"},{"name":"foetal methotrexate syndrome","type":"related"}],"termid":"MONDO:0016004","xrefs":{"Monarch":{"xref_id":"0016004"}}}


id: GO:2000289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of photoreceptor cell axon guidance.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of axon guidance","termid":"GO:1902667"},{"relation_name":"regulates","term_name":"photoreceptor cell axon guidance","termid":"GO:0072499"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of photoreceptor cell axon guidance","synonyms":[{"name":"regulation of photoreceptor cell axon pathfinding","type":"exact"}],"termid":"GO:2000289"}


id: PBO:0028814
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_primary_amine_oxidase_activity","termid":"PBO:0028814"}


id: FYPO:0005193
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of torin1 than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000139","FYPO:0002682","FYPO:0000003"],"is_obsolete":false,"name":"resistance to torin1","synonyms":[{"name":"resistance to torin 1","type":"exact"},{"name":"resistance to torin1 during mitotic cell cycle","type":"related"},{"name":"resistance to torin1 during vegetative growth","type":"exact"},{"name":"resistant to torin1","type":"exact"}],"termid":"FYPO:0005193"}


id: PBO:0081423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 280A","termid":"PBO:0081423"}


id: PBO:0058748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6872","termid":"PBO:0058748"}


id: MONDO:0007144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aortic arch interruption, facial palsy, and retinal coloboma","secondary_identifiers":["OMIM:107550","UMLS:C1862681","MESH:C566271","MEDGEN:350733"],"synonyms":[{"name":"aortic arch interruption, facial palsy, and retinal coloboma","type":"exact"}],"termid":"MONDO:0007144","xrefs":{"Monarch":{"xref_id":"0007144"}}}


id: FYPO:0000138
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_01143:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"711-723","gene_uniquename":"SJAG_01143","name":"mid1-delta(711-723 a.a.)","uniquename":"SJAG_01143:allele-2"},"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"},"SJAG_01834:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01834","name":"pom152delta","uniquename":"SJAG_01834:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_03250:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03250","name":"sst4delta","uniquename":"SJAG_03250:allele-1"},"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03449:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"man1DHEH","gene_uniquename":"SJAG_03449","name":"Man1DHEH","uniquename":"SJAG_03449:allele-2"},"SJAG_03449:allele-3":{"allele_type":"amino_acid_insertion_and_deletion","description":"man1-1-488","gene_uniquename":"SJAG_03449","name":"man1-1-488","uniquename":"SJAG_03449:allele-3"},"SJAG_03596:allele-1":{"allele_type":"amino_acid_mutation","description":"L264P,P442T","gene_uniquename":"SJAG_03596","name":"cdc15-A","uniquename":"SJAG_03596:allele-1"},"SJAG_03783:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03783","name":"vps24delta","uniquename":"SJAG_03783:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"},"SJAG_03892:allele-2":{"allele_type":"amino_acid_mutation","description":"E233Q","gene_uniquename":"SJAG_03892","name":"Vps4-EQ","uniquename":"SJAG_03892:allele-2"},"SJAG_03892:allele-3":{"allele_type":"amino_acid_mutation","description":"I307T L327S","gene_uniquename":"SJAG_03892","name":"vps4-ts","uniquename":"SJAG_03892:allele-3"},"SJAG_04280:allele-2":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-2"},"SJAG_04349:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04349","name":"vps28delta","uniquename":"SJAG_04349:allele-1"},"SJAG_04489:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04489","name":"did4delta","uniquename":"SJAG_04489:allele-1"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"},"SJAG_04912:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04912","name":"vps25delta","uniquename":"SJAG_04912:allele-1"},"SJAG_05207:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_05207","name":"cmp7delta","uniquename":"SJAG_05207:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007771"},{"annotations":[119581],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005503"},{"annotations":[119863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001132"},{"annotations":[119583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007177"},{"annotations":[119579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003946"},{"annotations":[119800],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"}],"single_locus_phenotype":[{"annotations":[119848,119850,119849],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001440"},{"annotations":[119860,119859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001370"},{"annotations":[119862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004718"},{"annotations":[119602,119601],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000731"},{"annotations":[119851,119827,119828,119854,119858,119834,119837,119855,119835,119857,119853,119856,119838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007771"},{"annotations":[119808,119806,119575,119805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005503"},{"annotations":[119905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001375"},{"annotations":[119584,119580,119572,119573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007177"},{"annotations":[119603],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0002026"},{"annotations":[119831],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007073"},{"annotations":[119807],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002870"},{"annotations":[119836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007770"},{"annotations":[119883,119882,119881,119885],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0004890"},{"annotations":[119801],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"},{"annotations":[119576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000644"},{"annotations":[119830],"is_not":false,"rel_names":["output_of","is_a"],"summary":null,"term":"FYPO:0003657"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype that affects the localization of a structure or substance in a cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process phenotype","termid":"FYPO:0000114"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00030":null,"SJAG_01050":null,"SJAG_01143":null,"SJAG_01665":null,"SJAG_01745":null,"SJAG_01794":null,"SJAG_01834":null,"SJAG_02392":null,"SJAG_03250":null,"SJAG_03449":null,"SJAG_03581":null,"SJAG_03596":null,"SJAG_03703":null,"SJAG_03783":null,"SJAG_03892":null,"SJAG_04280":null,"SJAG_04349":null,"SJAG_04489":null,"SJAG_04498":null,"SJAG_04522":null,"SJAG_04912":null,"SJAG_05207":null},"genotype_count":25,"genotypes_by_uniquename":{"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Man1DHEH(man1DHEH)","display_uniquename":"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-2","expression":"Not assayed or wild type"}]}]},"Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"Vps4-EQ(E233Q aa)","display_uniquename":"Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-2","expression":"Not assayed or wild type"}]}]},"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta":{"display_name":"cdc15-A(L264P,P442T aa) mid1delta","display_uniquename":"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03596:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"cmp7delta":{"display_name":"cmp7delta","display_uniquename":"cmp7delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_05207:allele-1","expression":"Null"}]}]},"cmp7delta__vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cmp7delta vps4-ts(I307T L327S aa)","display_uniquename":"cmp7delta__vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_05207:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-3","expression":"Not assayed or wild type"}]}]},"did4delta":{"display_name":"did4delta","display_uniquename":"did4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04489:allele-1","expression":"Null"}]}]},"lem2delta":{"display_name":"lem2delta","display_uniquename":"lem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01745:allele-1","expression":"Null"}]}]},"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type":{"display_name":"man1-1-488(aa)","display_uniquename":"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-3","expression":"Not assayed or wild type"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]},"mid1-delta(711-723_a.a.)-711-723-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"mid1-delta(711-723 a.a.)(aa)","display_uniquename":"mid1-delta(711-723_a.a.)-711-723-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-2","expression":"Not assayed or wild type"}]}]},"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"nur1delta":{"display_name":"nur1delta","display_uniquename":"nur1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]}]},"nur1delta__vps4delta":{"display_name":"nur1delta vps4delta","display_uniquename":"nur1delta__vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]},"pom152delta":{"display_name":"pom152delta","display_uniquename":"pom152delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01834:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]},"sst4delta":{"display_name":"sst4delta","display_uniquename":"sst4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03250:allele-1","expression":"Null"}]}]},"vps24delta":{"display_name":"vps24delta","display_uniquename":"vps24delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03783:allele-1","expression":"Null"}]}]},"vps25delta":{"display_name":"vps25delta","display_uniquename":"vps25delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04912:allele-1","expression":"Null"}]}]},"vps28delta":{"display_name":"vps28delta","display_uniquename":"vps28delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04349:allele-1","expression":"Null"}]}]},"vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"vps4-ts(I307T L327S aa)","display_uniquename":"vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-3","expression":"Not assayed or wild type"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]},"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"wee1-as8(T582G aa)","display_uniquename":"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]}},"in_subsets":["fypo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_01143","SJAG_01050","SJAG_04280","SJAG_03892","SJAG_03596","SJAG_04522","SJAG_05207","SJAG_02392"],"name":"localization phenotype","references_by_uniquename":{"PMID:24184107":null,"PMID:25866389":null,"PMID:30664646":null,"PMID:32109380":null,"PMID:32243490":null},"single_locus_annotated_genes":["SJAG_04912","SJAG_02392","SJAG_03449","SJAG_03783","SJAG_04280","SJAG_03892","SJAG_01745","SJAG_04489","SJAG_04349","SJAG_05207","SJAG_01050","SJAG_01143","SJAG_03250","SJAG_01834","SJAG_04522"],"single_locus_genotype_uniquenames":["Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type","mid1-delta(711-723_a.a.)-711-723-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","did4delta","vps25delta","vps28delta","pom1delta","lem2delta","wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","sst4delta","pom152delta","vps24delta","cmp7delta","mid1delta","nur1delta","vps4delta","vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","man1delta","rga4delta","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"fission yeast localization phenotype","type":"exact"},{"name":"localisation phenotype","type":"exact"}],"termid":"FYPO:0000138","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000338":null,"FYPO:0000644":null,"FYPO:0000731":null,"FYPO:0001132":null,"FYPO:0001369":null,"FYPO:0001370":null,"FYPO:0001375":null,"FYPO:0001440":null,"FYPO:0002026":null,"FYPO:0002870":null,"FYPO:0003657":null,"FYPO:0003946":null,"FYPO:0004718":null,"FYPO:0004890":null,"FYPO:0005503":null,"FYPO:0007073":null,"FYPO:0007177":null,"FYPO:0007770":null,"FYPO:0007771":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null,"GO:0000815":null}}


id: MONDO:0012831
data:
  {"annotated_genes":["SJAG_03363"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87713],"is_not":false,"summary":null,"term":"MONDO:0012831"}]},"cv_name":"mondo","definition":"Any inflammatory bowel disease in which the cause of the disease is a mutation in the ABCB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03363":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"inflammatory bowel disease 13","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0110893","MESH:C567384","MEDGEN:394202","OMIM:612244","UMLS:C2677101"],"synonyms":[{"name":"ABCB1 inflammatory bowel disease","type":"exact"},{"name":"IBD13","type":"exact"},{"name":"inflammatory bowel disease 13","type":"exact"},{"name":"inflammatory bowel disease caused by mutation in ABCB1","type":"exact"},{"name":"inflammatory bowel disease type 13","type":"exact"}],"termid":"MONDO:0012831","terms_by_termid":{"MONDO:0012831":null},"xrefs":{"Monarch":{"xref_id":"0012831"}}}


id: PBO:0085375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PINc domain endonuclease; required for early cleavage of 35S pre-rRNA and maturation of 18S rRNA; component of the SSU (small subunit) processome involved in 40S ribosomal subunit biogenesis; copurifies with Faf1p","termid":"PBO:0085375"}


id: GO:0019776
data:
  {"annotated_genes":["SJAG_06309","SJAG_01561","SJAG_03136"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72659,110083,110588],"is_not":false,"summary":null,"term":"GO:0019776"}]},"cv_name":"molecular_function","definition":"Catalysis of the covalent attachment of the ubiquitin-like protein Atg8 family modifier to phosphatidylethanolamine or phosphatidylserine on a membrane.","definition_xrefs":["PMID:12826404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein ligase activity","termid":"GO:0061659"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01561":null,"SJAG_03136":null,"SJAG_06309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0019787"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016740","GO:0016746","GO:0003824","GO:0003674","GO:0019787","GO:0140096"],"is_obsolete":false,"name":"Atg8-family ligase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5681981"],"synonyms":[{"name":"APG8 ligase activity","type":"exact"},{"name":"Atg8 ligase activity","type":"narrow"},{"name":"Atg8-like ligase activity","type":"exact"}],"termid":"GO:0019776","terms_by_termid":{"GO:0019776":null}}


id: GO:0033762
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a glucagon stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to peptide hormone","termid":"GO:0043434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to glucagon","synonyms":[{"name":"response to glucagon stimulus","type":"exact"}],"termid":"GO:0033762"}


id: PBO:0028445
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_mitotic_spindle_midzone_during_anaphase_B","termid":"PBO:0028445"}


id: GO:0036308
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + guanosine(1516) in 16S rRNA = N(2)-methylguanosine(1516) in 16S rRNA + S-adenosyl-L-homocysteine.","definition_xrefs":["GOC:imk","PMID:22079366"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA (guanine-N2-)-methyltransferase activity","termid":"GO:0008990"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003824","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"16S rRNA (guanine(1516)-N(2))-methyltransferase activity","termid":"GO:0036308"}


id: FYPO:0004463
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the nucleus is abolished when the cell is subject to glucose starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus","termid":"FYPO:0003450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to nucleus during glucose starvation","synonyms":[{"name":"abolished protein localisation to nucleus during glucose starvation","type":"exact"},{"name":"abolished protein localization to nucleus during glucose depletion","type":"exact"},{"name":"abolished protein localization to nucleus during glucose deprivation","type":"exact"},{"name":"abolished protein localization to nucleus during glucose limitation","type":"related"},{"name":"nuclear exclusion during glucose starvation","type":"related"},{"name":"nuclear protein exclusion during glucose starvation","type":"related"},{"name":"protein localization to nucleus abolished during glucose starvation","type":"exact"}],"termid":"FYPO:0004463"}


id: MONDO:0043168
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"fibrous dysplasia","termid":"MONDO:0000845"},{"relation_name":"is_a","term_name":"primary myelofibrosis","termid":"MONDO:0009692"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992","MONDO:0002280"],"is_obsolete":false,"name":"panostotic fibrous dysplasia","secondary_identifiers":["MESH:C537164","UMLS:C2931430","MEDGEN:419799"],"synonyms":[{"name":"unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemia","type":"related"}],"termid":"MONDO:0043168","xrefs":{"Monarch":{"xref_id":"0043168"}}}


id: PBO:0072417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 22","termid":"PBO:0072417"}


id: GO:0022615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial attachment of a protein to a target membrane, mediated by a proteins protruding from the target membrane. Docking requires only that the proteins come close enough to interact and adhere.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane docking","termid":"GO:0022406"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein to membrane docking","synonyms":[{"name":"protein-membrane docking","type":"exact"}],"termid":"GO:0022615"}


id: PBO:0041042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRCA1/BRCA2-containing complex subunit 3","termid":"PBO:0041042"}


id: PR:P30316
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cdc6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P30316"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase delta catalytic subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC336.04","synonyms":[{"name":"DNA polymerase III (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-cdc6","type":"exact"}],"termid":"PR:P30316"}


id: MOD:01239
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification produced by formation of an adduct of an L-histidine residue with 4-hydroxynonenal.","definition_xrefs":["PubMed:15133838","PubMed:10717661","Unimod:53#H","PubMed:11327326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-hydroxynonenal adduct","termid":"MOD:00446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"histidine 4-hydroxynonenal adduct","synonyms":[{"name":"4-hydroxynonenal (HNE)","type":"related"},{"name":"HNE","type":"related"}],"termid":"MOD:01239"}


id: GO:0010424
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent transfer of a methyl group to C-5 or N-4 of a cytosine located within a CG sequence in a DNA molecule.","definition_xrefs":["PMID:17239600","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA methylation on cytosine within a CG sequence (obsolete GO:0010424)","synonyms":[{"name":"cytosine methylation within a CG sequence","type":"exact"}],"termid":"GO:0010424"}


id: PBO:0046202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELOA pseudogene 1","termid":"PBO:0046202"}


id: PBO:0076764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tudor domain containing 1","termid":"PBO:0076764"}


id: MONDO:0008658
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete virus Rd114 RNA Complementarity (obsolete MONDO:0008658)","secondary_identifiers":["OMIM:193070"],"synonyms":[{"name":"virus Rd114 RNA Complementarity","type":"exact"}],"termid":"MONDO:0008658","xrefs":{"Monarch":{"xref_id":"0008658"}}}


id: PBO:0000410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy C terminal domain family protein (predicted)","termid":"PBO:0000410"}


id: PBO:0065772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Q-nucleotide N-glycosylase 1","termid":"PBO:0065772"}


id: PBO:0060823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nectin cell adhesion molecule 1","termid":"PBO:0060823"}


id: PBO:0005811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin Sal3","termid":"PBO:0005811"}


id: PBO:0051864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster assembly enzyme pseudogene 1","termid":"PBO:0051864"}


id: PR:O74838
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- wtf10 gene.","definition_xrefs":["UniProtKB:O74838","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein wtf10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.10","synonyms":[{"name":"Spom972h-wtf10","type":"exact"}],"termid":"PR:O74838"}


id: GO:0042413
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of carnitine (hydroxy-trimethyl aminobutyric acid), a compound that participates in the transfer of acyl groups across the inner mitochondrial membrane.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid betaine catabolic process","termid":"GO:0006579"},{"relation_name":"is_a","term_name":"carnitine metabolic process","termid":"GO:0009437"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"carnitine catabolic process","synonyms":[{"name":"carnitine breakdown","type":"exact"},{"name":"carnitine catabolism","type":"exact"},{"name":"carnitine degradation","type":"exact"},{"name":"vitamin Bt catabolic process","type":"exact"},{"name":"vitamin Bt catabolism","type":"exact"}],"termid":"GO:0042413"}


id: PBO:0085730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in the regulation of endocytosis; transiently recruited to actin cortical patches in a SLA1-dependent manner after late coat component assembly; GFP-fusion protein localizes to the periphery, cytoplasm, bud, and bud neck","termid":"PBO:0085730"}


id: PBO:0041002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BORA aurora kinase A activator","termid":"PBO:0041002"}


id: FYPO:0000585
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which ascospore wall biogenesis does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal ascospore wall biogenesis","termid":"FYPO:0000580"},{"relation_name":"is_a","term_name":"abolished cell wall biogenesis","termid":"FYPO:0003639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000121"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000121","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"abolished ascospore wall biogenesis","synonyms":[{"name":"absent spore wall formation","type":"related"},{"name":"ascospore wall biogenesis abolished","type":"exact"},{"name":"spore wall formation abolished","type":"related"},{"name":"spore wall formation: absent","type":"related"}],"termid":"FYPO:0000585"}


id: SO:0000851
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a CDS.","definition_xrefs":["SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA_region","termid":"SO:0000836"},{"relation_name":"part_of","term_name":"CDS","termid":"SO:0000316"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDS_region","synonyms":[{"name":"CDS region","type":"exact"}],"termid":"SO:0000851"}


id: FYPO:0000670
data:
  {"alleles_by_uniquename":{"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03449:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"man1DHEH","gene_uniquename":"SJAG_03449","name":"Man1DHEH","uniquename":"SJAG_03449:allele-2"},"SJAG_03449:allele-3":{"allele_type":"amino_acid_insertion_and_deletion","description":"man1-1-488","gene_uniquename":"SJAG_03449","name":"man1-1-488","uniquename":"SJAG_03449:allele-3"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119888,119889,119890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000671"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid separation is abnormal. Mitotic sister chromatid separation is the process in which sister chromatids are physically detached from each other during mitosis.","definition_xrefs":["GO:0051306","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"part_of","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03449":null},"genotype_count":3,"genotypes_by_uniquename":{"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Man1DHEH(man1DHEH)","display_uniquename":"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-2","expression":"Not assayed or wild type"}]}]},"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type":{"display_name":"man1-1-488(aa)","display_uniquename":"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-3","expression":"Not assayed or wild type"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000337","FYPO:0000641","FYPO:0001320","FYPO:0000631"],"is_obsolete":false,"name":"abnormal mitotic sister chromatid separation","references_by_uniquename":{"PMID:24184107":null},"single_locus_annotated_genes":["SJAG_03449"],"single_locus_genotype_uniquenames":["man1delta","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal mitotic chromosome separation","type":"exact"},{"name":"abnormal sister chromatid separation during mitosis","type":"exact"},{"name":"abnormal sister chromatid separation during mitotic cell cycle","type":"related"},{"name":"abnormal sister chromatid separation during vegetative growth","type":"exact"},{"name":"aneuploidy","type":"related"},{"name":"mitotic chromosome missegregation","type":"related"}],"termid":"FYPO:0000670","terms_by_termid":{"FYPO:0000671":null}}


id: MONDO:1012589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculocutaneous albinism that occurs in Japanese medaka due to a mutation in the TYR gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism, non-human animal","termid":"MONDO:1012579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculocutaneous albinism, TYR-related, Japanese medaka","secondary_identifiers":["OMIA:000202-8090"],"synonyms":[{"name":"coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related in Oryzias latipes (Japanese medaka)","type":"exact"}],"termid":"MONDO:1012589","xrefs":{"Monarch":{"xref_id":"1012589"}}}


id: PBO:0000846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Vip1","termid":"PBO:0000846"}


id: PBO:0067907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 209","termid":"PBO:0067907"}


id: GO:0071438
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The portion of the plasma membrane surrounding an invadopodium.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete invadopodium membrane (obsolete GO:0071438)","termid":"GO:0071438"}


id: GO:0038013
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which internalization of a Wnt receptor activates or increases the frequency, rate or extent of the Wnt signaling pathway.","definition_xrefs":["GOC:signaling","PMID:17908284","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of Wnt signaling pathway by Wnt receptor internalization (obsolete GO:0038013)","synonyms":[{"name":"positive regulation of Wnt receptor signaling pathway by Frizzled internalization","type":"related"},{"name":"positive regulation of Wnt receptor signaling pathway by LRP6 internalization","type":"narrow"},{"name":"positive regulation of Wnt receptor signaling pathway by Wnt receptor internalization","type":"exact"},{"name":"positive regulation of Wnt receptor signalling pathway by Wnt receptor endocytosis","type":"exact"},{"name":"positive regulation of Wnt-activated signaling pathway by Wnt receptor internalization","type":"related"}],"termid":"GO:0038013"}


id: GO:0033988
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7alpha,12alpha-dihydroxy-3-oxochol-4-en-24-oate = 12alpha-hydroxy-3-oxochola-4,6-dien-24-oate + H2O.","definition_xrefs":["PMID:26650892","RHEA:10436"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"bile-acid 7alpha-dehydratase activity","secondary_identifiers":["EC:4.2.1.106","MetaCyc:BA7DEHYDRA-RXN","KEGG_REACTION:R07318"],"synonyms":[{"name":"7alpha,12alpha-dihydroxy-3-oxochol-4-enoate hydro-lyase (12alpha-hydroxy-3-oxochola-4,6-dienoate-forming) activity","type":"related"},{"name":"7alpha,12alpha-dihydroxy-3-oxochol-4-enoate hydro-lyase activity","type":"related"},{"name":"BA7 alpha dehydratase activity","type":"related"}],"termid":"GO:0033988"}


id: MONDO:0024876
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease that involves the tendon sheath.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disease of the tendon","termid":"MONDO:0100010"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tendon sheath disorder","secondary_identifiers":["ICD9:727.9","UMLS:C0729734","MEDGEN:675994","SCTID:312381009"],"synonyms":[{"name":"disease of tendon sheath","type":"exact"},{"name":"disease or disorder of tendon sheath","type":"exact"},{"name":"disorder of tendon sheath","type":"exact"},{"name":"tendon sheath disease","type":"exact"},{"name":"tendon sheath disease or disorder","type":"exact"},{"name":"tendon sheath disorder","type":"exact"}],"termid":"MONDO:0024876","xrefs":{"Monarch":{"xref_id":"0024876"}}}


id: PBO:0048003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FRMD4A antisense RNA 1","termid":"PBO:0048003"}


id: GO:0009107
data:
  {"annotated_genes":["SJAG_03198","SJAG_01271","SJAG_03553"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75490,97494,98191],"is_not":false,"summary":null,"term":"GO:0009107"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lipoate, 1,2-dithiolane-3-pentanoate, the anion derived from lipoic acid.","definition_xrefs":["GOC:ai","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid biosynthetic process","termid":"GO:0006633"},{"relation_name":"is_a","term_name":"lipoate metabolic process","termid":"GO:0009106"},{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01271":null,"SJAG_03198":null,"SJAG_03553":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006790","GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"lipoate biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0009105"],"synonyms":[{"name":"lipoate anabolism","type":"exact"},{"name":"lipoate biosynthesis","type":"exact"},{"name":"lipoate formation","type":"exact"},{"name":"lipoate synthesis","type":"exact"},{"name":"lipoic acid anabolism","type":"exact"},{"name":"lipoic acid biosynthesis","type":"exact"},{"name":"lipoic acid biosynthetic process","type":"exact"},{"name":"lipoic acid formation","type":"exact"},{"name":"lipoic acid synthesis","type":"exact"}],"termid":"GO:0009107","terms_by_termid":{"GO:0009107":null}}


id: FYPO:0001871
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell adhesion phenotype in which cells adhere to other cells of compatible mating type more strongly or to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell adhesion","termid":"FYPO:0001872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased agglutination","synonyms":[{"name":"increased agglutination involved in conjugation with cellular fusion","type":"exact"}],"termid":"FYPO:0001871"}


id: PBO:0074287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLIT and NTRK like family member 2","termid":"PBO:0074287"}


id: GO:0009517
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Protein-pigment complex associated with photosystem II.","definition_xrefs":["ISBN:0582227089","GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thylakoid light-harvesting complex","termid":"GO:0009503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"PSII associated light-harvesting complex II","synonyms":[{"name":"LHCII","type":"exact"}],"termid":"GO:0009517"}


id: GO:0052694
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: jasmonoyl-isoleucine + NADPH + H+ + O2 = 12-hydroxy-jasmonoyl-isoleucine + NADP+ + H2O.","definition_xrefs":["MetaCyc:RXN-12421","PMID:21576464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"jasmonoyl-isoleucine-12-hydroxylase activity","secondary_identifiers":["RHEA:54808"],"termid":"GO:0052694"}


id: PBO:0068174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 481","termid":"PBO:0068174"}


id: MONDO:0018431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete autosomal recessive hereditary sensory and autonomic neuropathy (obsolete MONDO:0015366)","termid":"MONDO:0015366"},{"relation_name":"is_a","term_name":"hereditary sensory and autonomic neuropathy","termid":"MONDO:0015364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"cold-induced sweating syndrome - hyperthermia spectrum","secondary_identifiers":["GARD:21708","MEDGEN:1842440","UMLS:C5681139","Orphanet:401993"],"termid":"MONDO:0018431","xrefs":{"Monarch":{"xref_id":"0018431"}}}


id: GO:0050628
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetoacetate + coenzyme M + NADP+ = 2-oxopropyl-coenzyme M + CO2 + NADPH.","definition_xrefs":["EC:1.8.1.5","RHEA:16977"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor","termid":"GO:0016668"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"2-oxopropyl-CoM reductase (carboxylating) activity","secondary_identifiers":["UM-BBD_reactionID:r0854","MetaCyc:1.8.1.5-RXN","KEGG_REACTION:R05713"],"synonyms":[{"name":"2-KPCC activity","type":"related"},{"name":"2-mercaptoethanesulfonate,acetoacetate:NADP+ oxidoreductase (decarboxylating)","type":"related"},{"name":"NADPH:2-(2-ketopropylthio)ethanesulfonate oxidoreductase/carboxylase activity","type":"related"},{"name":"NADPH:2-ketopropyl-coenzyme M oxidoreductase/carboxylase activity","type":"related"}],"termid":"GO:0050628"}


id: MONDO:0000618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"breast carcinoma by gene expression profile","termid":"MONDO:0006116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"Her2-receptor negative breast cancer","secondary_identifiers":["EFO:0009780","NCIT:C168519","MEDGEN:1684659","UMLS:C4733095","SCTID:431396003","DOID:0060080"],"termid":"MONDO:0000618","xrefs":{"Monarch":{"xref_id":"0000618"}}}


id: MONDO:0018905
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diffuse large B-cell lymphoma is the most common subtype of non-Hodgkin lymphoma (NHL) in adults characterized by a median age of presentation in the sixth decade of life (but also rarely occurring in adolescents and children) with the initial presentation being single or multiple rapidly growing masses (that may or may not be painful) in nodal or extranodal sites (such as thyroid, skin, breast, gastrointestinal tract, testes, bone, or brain) and that can be accompanied by symptoms of fever, night sweats and weight loss. DLBCL has an aggressive disease course, with the elderly having a poorer prognosis than younger patients, and with relapses being common.","definition_xrefs":["Orphanet:544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm of mature B-cells","termid":"MONDO:0004949"},{"relation_name":"is_a","term_name":"aggressive B-cell non-Hodgkin lymphoma","termid":"MONDO:0017595"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"diffuse large B-cell lymphoma","secondary_identifiers":["UMLS:C0079744","EFO:0000403","GARD:3178","DOID:0050745","NCIT:C8851","icd11.foundation:1946973604","MEDGEN:86954","MESH:D016403","ICD9:200.7","ICDO:9680/3","MedDRA:10012818"],"synonyms":[{"name":"DLBCL","type":"exact"},{"name":"diffuse large B-cell lymphoma","type":"exact"}],"termid":"MONDO:0018905","xrefs":{"Monarch":{"xref_id":"0018905"}}}


id: PR:Q10231
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A lanosterol synthase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00950"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lanosterol synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13G7.01c","secondary_identifiers":["UniProtKB:Q10231"],"synonyms":[{"name":"2,3-epoxysqualene--lanosterol cyclase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"OSC (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-LSS","type":"exact"},{"name":"oxidosqualene--lanosterol cyclase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10231"}


id: PBO:0047057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 118 member A","termid":"PBO:0047057"}


id: GO:0005604
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen-containing extracellular matrix consisting of a thin layer of dense material found in various animal tissues interposed between the cells and the adjacent connective tissue. It consists of the basal lamina plus an associated layer of reticulin fibers.","definition_xrefs":["PMID:33605520","PMID:39223427","PMID:22505934"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix","termid":"GO:0031012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"basement membrane","secondary_identifiers":["Wikipedia:Basement_membrane","GO:0005605","GO:0008003"],"synonyms":[{"name":"basal lamina","type":"related"},{"name":"basement lamina","type":"related"},{"name":"lamina densa","type":"related"}],"termid":"GO:0005604"}


id: FYPO:0007792
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a smaller than normal proportion of cells in the population remains viable when cells the population are subject to magnesium starvation.","definition_xrefs":["PMID:33970532","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"loss of viability upon nutrient depletion","termid":"FYPO:0000244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"loss of viability upon magnesium starvation","synonyms":[{"name":"decreased viability upon magnesium starvation","type":"exact"},{"name":"loss of cell population viability upon magnesium starvation","type":"exact"},{"name":"loss of viability upon magnesium depletion","type":"exact"},{"name":"loss of viability upon magnesium deprivation","type":"exact"},{"name":"loss of viability upon magnesium limitation","type":"exact"},{"name":"reduced viability upon magnesium starvation","type":"exact"}],"termid":"FYPO:0007792"}


id: GO:0046387
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving deoxyribose 1,5-bisphosphate, the diphosphorylated sugar 1,5-diphospho-2-deoxyribose.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyribose phosphate metabolic process","termid":"GO:0019692"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"deoxyribose 1,5-bisphosphate metabolic process","synonyms":[{"name":"deoxyribose 1,5-bisphosphate metabolism","type":"exact"}],"termid":"GO:0046387"}


id: PBO:0087384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sterol regulatory element binding protein; induces sterol biosynthetic genes, upon sterol depletion; acts as a sterol sensor, binding ergosterol in sterol rich conditions; relocates from intracellular membranes to perinuclear foci upon sterol depletion; redundant activator of filamentation with ECM22, up-regulating the expression of filamentous growth genes; contains a Zn[2]-Cys[6] binuclear cluster; UPC2 has a paralog, ECM22, that arose from the whole genome duplication","termid":"PBO:0087384"}


id: MONDO:1011279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Age-related macular degeneration that occurs in Rhesus monkey.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"age-related macular degeneration, non-human animal","termid":"MONDO:1010351"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"age-related macular degeneration, Rhesus monkey","secondary_identifiers":["OMIA:002142-9544"],"termid":"MONDO:1011279","xrefs":{"Monarch":{"xref_id":"1011279"}}}


id: MONDO:0700202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bunyaviridae infectious disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bunyaviridae infectious disease, non-human animal","termid":"MONDO:0700202","xrefs":{"Monarch":{"xref_id":"0700202"}}}


id: MONDO:0002303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Blockage of the central retinal vein.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vein disorder","termid":"MONDO:0004634"},{"relation_name":"is_a","term_name":"retinal vein occlusion","termid":"MONDO:0006951"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"central retinal vein occlusion","secondary_identifiers":["SCTID:68478007","UMLS:C0154841","icd11.foundation:1146548497","MEDGEN:509679","NCIT:C118859","Orphanet:411527","GARD:21734","DOID:2450","ICD9:362.35"],"synonyms":[{"name":"central retinal Venous occlusion","type":"exact"},{"name":"central retinal vein retinal vein occlusion","type":"exact"},{"name":"retinal vein occlusion of central retinal vein","type":"exact"}],"termid":"MONDO:0002303","xrefs":{"Monarch":{"xref_id":"0002303"}}}


id: PBO:0069845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1131, pseudogene","termid":"PBO:0069845"}


id: MONDO:0012638
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microphthalmia-brain atrophy (MOBA) syndrome is a rare genetic neurodegenerative disorder characterized by congenital microphthalmia, sunken eyes, blindness, microcephaly, severe intellectual disability, progressive spasticity, and seizures. Psychomotor development is normal in the first 6-8 months of life and thereafter declines rapidly and continuously. Brain MRI reveals progressive and extensive degenerative changes, especially cortex, cerebellum, brainstem, and corpus callosum atrophy, with complete loss of cerebral white matter.","definition_xrefs":["Orphanet:77299"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"eye degenerative disorder","termid":"MONDO:0004884"},{"relation_name":"is_a","term_name":"syndromic microphthalmia","termid":"MONDO:0016073"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005559"],"is_obsolete":false,"name":"microphthalmia-brain atrophy syndrome","secondary_identifiers":["OMIM:611222","MESH:C566985","MEDGEN:370809","SCTID:720010009","UMLS:C1970013","GARD:9292","DOID:0111812"],"synonyms":[{"name":"MCOPS10","type":"exact"},{"name":"MOBA","type":"related"},{"name":"MOBA syndrome","type":"exact"},{"name":"microphthalmia and brain atrophy","type":"related"},{"name":"microphthalmia syndromic 10","type":"related"},{"name":"microphthalmia, syndromic 10","type":"related"},{"name":"syndromic microphthalmia type 10","type":"exact"}],"termid":"MONDO:0012638","xrefs":{"Monarch":{"xref_id":"0012638"}}}


id: MONDO:0024532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any otofaciocervical syndrome in which the cause of the disease is a mutation in the EYA1 gene.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otofaciocervical syndrome","termid":"MONDO:0008163"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otofaciocervical syndrome 1","secondary_identifiers":["UMLS:C3714941","MEDGEN:811516","GARD:16502","OMIM:166780"],"synonyms":[{"name":"EYA1 otofaciocervical syndrome","type":"exact"},{"name":"OFC","type":"broad"},{"name":"OFC1","type":"related"},{"name":"OTFCS","type":"broad"},{"name":"otofaciocervical syndrome","type":"broad"},{"name":"otofaciocervical syndrome 1","type":"exact"},{"name":"otofaciocervical syndrome caused by mutation in EYA1","type":"exact"}],"termid":"MONDO:0024532","xrefs":{"Monarch":{"xref_id":"0024532"}}}


id: GO:0035759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The binding of a mesangial cell to the extracellular matrix via adhesion molecules. A mesangial cell is a cell that encapsulates the capillaries and venules in the kidney.","definition_xrefs":["PMID:15569314","GOC:BHF","CL:0000650"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-matrix adhesion","termid":"GO:0007160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"mesangial cell-matrix adhesion","termid":"GO:0035759"}


id: PBO:0062198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily U member 1 pseudogene","termid":"PBO:0062198"}


id: GO:0020036
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A disk-like structure that appears at the periphery of a red blood cell infected by an apicomplexan parasite, characterized by a translucent lumen and an electron-dense coat of variable thickness; often appears to be tethered to the host cell membrane by fibrous connections with the erythrocyte cytoskeleton.","definition_xrefs":["PMID:16705161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell cytoplasm part","termid":"GO:0033655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"Maurer's cleft","synonyms":[{"name":"Maurers cleft","type":"exact"}],"termid":"GO:0020036"}


id: MONDO:0003606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the adrenal medulla","direct_ancestors":[{"relation_name":"is_a","term_name":"adrenal gland cancer","termid":"MONDO:0002817"},{"relation_name":"is_a","term_name":"adrenal medulla neoplasm","termid":"MONDO:0021237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"adrenal medulla cancer","secondary_identifiers":["NCIT:C4396","GARD:5755","DOID:5719","MEDGEN:87485","UMLS:C0344456","SCTID:371965009"],"synonyms":[{"name":"adrenal medulla cancer","type":"exact"},{"name":"adrenal medulla neoplasm","type":"broad"},{"name":"adrenal medulla tumor","type":"broad"},{"name":"adrenal medulla tumour","type":"broad"},{"name":"cancer of adrenal medulla","type":"exact"},{"name":"malignant adrenal medulla neoplasm","type":"exact"},{"name":"malignant adrenal medulla tumor","type":"exact"},{"name":"malignant adrenal medulla tumour","type":"exact"},{"name":"malignant neoplasm of adrenal medulla","type":"exact"},{"name":"malignant neoplasm of the adrenal medulla","type":"exact"},{"name":"malignant tumor of adrenal medulla","type":"exact"},{"name":"malignant tumor of the adrenal medulla","type":"exact"},{"name":"malignant tumour of adrenal medulla","type":"exact"},{"name":"malignant tumour of the adrenal medulla","type":"exact"}],"termid":"MONDO:0003606","xrefs":{"Monarch":{"xref_id":"0003606"}}}


id: PBO:0068830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 68, pseudogene","termid":"PBO:0068830"}


id: MONDO:0024643
data:
  {"annotated_genes":["SJAG_03081"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859173"}]},"cv_name":"mondo","definition":"A disorder that affects the muscle tissue of the heart. Representative examples include myocardial infarction, myocarditis, and cardiomyopathy.","definition_xrefs":["NCIT:C35544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03081":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"myocardial disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:469033","UMLS:C3241958","SCTID:57809008"],"synonyms":[{"name":"disease of myocardium","type":"exact"},{"name":"disease or disorder of myocardium","type":"exact"},{"name":"disorder of heart muscle","type":"related"},{"name":"disorder of myocardium","type":"exact"},{"name":"myocardial disease","type":"exact"},{"name":"myocardial disorder","type":"exact"},{"name":"myocardium disease","type":"exact"},{"name":"myocardium disease or disorder","type":"exact"}],"termid":"MONDO:0024643","terms_by_termid":{"MONDO:0859173":null},"xrefs":{"Monarch":{"xref_id":"0024643"}}}


id: MONDO:0014961
data:
  {"annotated_genes":["SJAG_05196"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87536],"is_not":false,"summary":null,"term":"MONDO:0014961"}]},"cv_name":"mondo","definition":"Any azoospermia in which the cause of the disease is a mutation in the SUN5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05196":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 16","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070184","MEDGEN:934641","OMIM:617187","UMLS:C4310674"],"synonyms":[{"name":"SPGF16","type":"exact"},{"name":"SUN5 azoospermia","type":"exact"},{"name":"acephalic spermatozoa syndrome","type":"related"},{"name":"azoospermia caused by mutation in SUN5","type":"exact"},{"name":"spermatogenic failure 16","type":"exact"},{"name":"spermatogenic failure 16; SPGF16","type":"exact"},{"name":"spermatogenic failure type 16","type":"exact"}],"termid":"MONDO:0014961","terms_by_termid":{"MONDO:0014961":null},"xrefs":{"Monarch":{"xref_id":"0014961"}}}


id: FYPO:0002777
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the sumoylation of one or more specific proteins, or of specific protein sites, is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification during vegetative growth","termid":"FYPO:0000329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0001985","FYPO:0005447","FYPO:0002494","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal protein sumoylation during vegetative growth","synonyms":[{"name":"abnormal protein sumolation during vegetative growth","type":"exact"},{"name":"abnormal protein sumoylation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002777"}


id: PBO:0091858
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribose methyltransferase Mrm1","termid":"PBO:0091858"}


id: MONDO:0009614
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive form of methylmalonic aciduria, caused by mutation(s) in the MMAB gene, encoding cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial.","definition_xrefs":["NCIT:C142172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin B12-responsive methylmalonic acidemia","termid":"MONDO:0017214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"methylmalonic aciduria, cblB type","secondary_identifiers":["NANDO:1200796","OMIM:251110","MEDGEN:344420","Orphanet:79311","GARD:9479","DOID:0060743","NANDO:2201106","UMLS:C1855102"],"synonyms":[{"name":"methylmalonic acidemia cblB type","type":"exact"},{"name":"methylmalonic acidemia, cblB type","type":"exact"},{"name":"methylmalonic aciduria cblB type","type":"exact"},{"name":"methylmalonic aciduria, cblB type","type":"exact"},{"name":"methylmalonic aciduria, vitamin B12-responsive, cblB type","type":"exact"},{"name":"methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type","type":"exact"},{"name":"methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB type","type":"related"},{"name":"vitamin B12-responsive methylmalonic acidemia type cblB","type":"exact"},{"name":"vitamin B12-responsive methylmalonic aciduria, type cblB","type":"exact"}],"termid":"MONDO:0009614","xrefs":{"Monarch":{"xref_id":"0009614"}}}


id: MONDO:0009406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cantu syndrome is a rare disorder characterized by congenital hypertrichosis, osteochondrodysplasia, cardiomegaly, and dysmorphism.","definition_xrefs":["Orphanet:1517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"hypertrichotic osteochondrodysplasia Cantu type","secondary_identifiers":["UMLS:C0795905","DOID:0060569","GARD:8585","OMIM:239850","SCTID:239087008","MEDGEN:208647","MESH:C535572"],"synonyms":[{"name":"Cantu syndrome","type":"exact"},{"name":"Craniofaciocardioskeletal syndrome","type":"related"},{"name":"hypertrichotic osteochondrodysplasia","type":"related"},{"name":"hypertrichotic osteochondrodysplasia (Cantu syndrome)","type":"exact"},{"name":"hypertrichotic osteochondrodysplasia, Cantu type","type":"related"}],"termid":"MONDO:0009406","xrefs":{"Monarch":{"xref_id":"0009406"}}}


id: PBO:0067841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 143","termid":"PBO:0067841"}


id: PBO:0030325
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_actin_cortical_patch_localization","termid":"PBO:0030325"}


id: MONDO:0020579
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the mucous membranes.","definition_xrefs":["NCIT:C115965"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucositis","secondary_identifiers":["MESH:D052016","MEDGEN:87165","UMLS:C0333355"],"synonyms":[{"name":"inflammation of mucosa","type":"exact"},{"name":"mucosa inflammation","type":"exact"},{"name":"mucositis","type":"exact"}],"termid":"MONDO:0020579","xrefs":{"Monarch":{"xref_id":"0020579"}}}


id: GO:0048447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the sepal are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floral organ morphogenesis","termid":"GO:0048444"},{"relation_name":"part_of","term_name":"sepal development","termid":"GO:0048442"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"sepal morphogenesis","secondary_identifiers":["GO:0048422"],"termid":"GO:0048447"}


id: PBO:0048968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPALPP motifs containing 1","termid":"PBO:0048968"}


id: GO:0019439
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of aromatic compounds, any substance containing an aromatic carbon ring.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete aromatic compound catabolic process (obsolete GO:0019439)","termid":"GO:0019439"}


id: MONDO:0010090
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Summitt syndrome is an extremely rare disorder originally described in two brothers and characterized by mild to severe craniosynostosis and syndactyly, obesity, and normal intelligence. Acrocephaly, brachydactyly, clinodactyly, mild syndactyly of the hands and feet, genu valgum and marked obesity were later described in another patient. There have been no further descriptions in the literature since 1979. Summitt syndrome could be a variant of Carpenter syndrome.","definition_xrefs":["Orphanet:3210"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"Summitt syndrome","secondary_identifiers":["MESH:C538142","UMLS:C1802405","ICD10CM:Q82.0","NORD:1746","OMIM:272350","SCTID:733606001","GARD:127","MEDGEN:369198"],"synonyms":[{"name":"Summitt syndrome","type":"exact"},{"name":"Summitt's acrocephalosyndactyly","type":"related"},{"name":"recessive acrocephalosyndactyly with normal intelligence","type":"related"}],"termid":"MONDO:0010090","xrefs":{"Monarch":{"xref_id":"0010090"}}}


id: MONDO:0016548
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Megacystic-megaureter syndrome is an urinary tract malformation characterized by the presence of a massive primary non-obstructive vesicoureteral reflux and a large capacity, smooth, thin walled bladder due to the continual recycling of refluxed urine. Recurrent urinary infections are commonly associated with this condition.","definition_xrefs":["Orphanet:238637"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary system disorder","termid":"MONDO:0002118"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megacystis-megaureter syndrome","secondary_identifiers":["GARD:20638","icd11.foundation:1872503107","MEDGEN:609133","SCTID:253904001","UMLS:C0431752"],"synonyms":[{"name":"megaureter-megacystis syndrome","type":"exact"}],"termid":"MONDO:0016548","xrefs":{"Monarch":{"xref_id":"0016548"}}}


id: PR:000044588
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the sid4 gene in Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septation initiation protein sid4 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC244.01c","synonyms":[{"name":"Spom-sid4","type":"exact"}],"termid":"PR:000044588"}


id: GO:0005173
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a stem cell factor receptor (SCFR), a type III transmembrane kinase receptor.","definition_xrefs":["PMID:10698217","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor binding","termid":"GO:0005126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"stem cell factor receptor binding","synonyms":[{"name":"KIT binding","type":"narrow"},{"name":"SCF","type":"narrow"},{"name":"SCFR binding","type":"exact"},{"name":"stem cell factor","type":"narrow"},{"name":"stem cell factor receptor ligand","type":"narrow"}],"termid":"GO:0005173"}


id: MONDO:0002556
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The rarest histopathologic subtype of Schwannoma. The reported cases have been located in the gastrointestinal submucosa or subcutaneous tissue. Morphologically it is characterized by the presence of a microcyst-rich network of spindle cells with minimal amount of cytoplasm and Antoni A tissue.","definition_xrefs":["NCIT:C5321"],"direct_ancestors":[{"relation_name":"is_a","term_name":"schwannoma","termid":"MONDO:0002546"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microcystic/reticular schwannoma","secondary_identifiers":["MEDGEN:882329","UMLS:C4054526"],"synonyms":[{"name":"microcystic/reticular schwannoma","type":"exact"}],"termid":"MONDO:0002556","xrefs":{"Monarch":{"xref_id":"0002556"}}}


id: GO:0047687
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-ascorbate + H2O + O2 = L-threonate + 2 H+ + oxalate.","definition_xrefs":["EC:1.13.11.13"],"gene_count":0,"genotype_count":0,"name":"obsolete ascorbate 2,3-dioxygenase activity (obsolete GO:0047687)","synonyms":[{"name":"AAoxygenase activity","type":"exact"},{"name":"ascorbate 2,3-dioxygenase activity","type":"exact"},{"name":"ascorbate:oxygen 2,3-oxidoreductase (bond-cleaving)","type":"exact"}],"termid":"GO:0047687"}


id: MONDO:1012200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal motility disorder, non-human animal","termid":"MONDO:1011661"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"esophageal motility disorder, dog","secondary_identifiers":["OMIA:000738-9615"],"termid":"MONDO:1012200","xrefs":{"Monarch":{"xref_id":"1012200"}}}


id: PBO:0081219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc metallopeptidase STE24","termid":"PBO:0081219"}


id: FYPO:0004133
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of reactive oxygen species (ROS) measured in a cell that is subject to nitrogen starvation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell","termid":"FYPO:0001076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal reactive oxygen species level during nitrogen starvation","synonyms":[{"name":"normal ROS accumulation during nitrogen starvation","type":"related"},{"name":"normal ROS level during nitrogen starvation","type":"exact"},{"name":"normal cellular reactive oxygen species level during nitrogen starvation","type":"exact"},{"name":"normal reactive oxygen species level during nitrogen depletion","type":"exact"},{"name":"normal reactive oxygen species level during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0004133"}


id: PBO:0088602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"7,8-diamino-pelargonic acid aminotransferase (DAPA)","termid":"PBO:0088602"}


id: MONDO:1010272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Renal agenesis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"renal disease, non-human animal","termid":"MONDO:1011909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"renal agenesis, non-human animal","secondary_identifiers":["OMIA:002007"],"termid":"MONDO:1010272","xrefs":{"Monarch":{"xref_id":"1010272"}}}


id: PBO:0071432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 38","termid":"PBO:0071432"}


id: PBO:0113759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein, lipocalin-like","termid":"PBO:0113759"}


id: GO:0071708
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which immunoglobulin light chain V and J gene segments are recombined within a single locus utilizing the conserved heptamer and nonomer recombination signal sequences (RSS).","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin V(D)J recombination","termid":"GO:0033152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006310","GO:0010467","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"immunoglobulin light chain V-J recombination","synonyms":[{"name":"immunoglobulin V(D)J joining","type":"broad"},{"name":"immunoglobulin V(D)J recombination","type":"broad"},{"name":"immunoglobulin V-J joining","type":"exact"}],"termid":"GO:0071708"}


id: GO:0060965
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that decreases the rate, frequency, or extent of gene silencing by a microRNA (miRNA).","definition_xrefs":["GOC:aruk","GOC:dph","PMID:28379604","GOC:bc","GOC:rl","GOC:tb","PMID:23985560"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of miRNA-mediated gene silencing","termid":"GO:0060964"},{"relation_name":"is_a","term_name":"negative regulation of post-transcriptional gene silencing by regulatory ncRNA","termid":"GO:1900369"},{"relation_name":"negatively_regulates","term_name":"miRNA-mediated post-transcriptional gene silencing","termid":"GO:0035195"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of miRNA-mediated gene silencing","synonyms":[{"name":"negative regulation of gene silencing by miRNA","type":"exact"},{"name":"negative regulation of gene silencing by microRNA","type":"exact"}],"termid":"GO:0060965"}


id: PBO:0035946
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_spatial_extent_of_histone_H2B-K119_ubiquitination_at_double-strand_break_site_during_vegetative_growth","termid":"PBO:0035946"}


id: GO:0015184
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of L-cystine from one side of a membrane to the other.","definition_xrefs":["GOC:mtg_transport","ISBN:0198506732","GOC:go_curators","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur amino acid transmembrane transporter activity","termid":"GO:0000099"},{"relation_name":"is_a","term_name":"L-amino acid transmembrane transporter activity","termid":"GO:0015179"},{"relation_name":"is_a","term_name":"modified amino acid transmembrane transporter activity","termid":"GO:0072349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"L-cystine transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-5340130"],"synonyms":[{"name":"L-cystine transporter activity","type":"broad"},{"name":"cystine/diaminopimelate porter activity","type":"narrow"}],"termid":"GO:0015184"}


id: GO:1900101
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endoplasmic reticulum unfolded protein response.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"is_a","term_name":"regulation of response to endoplasmic reticulum stress","termid":"GO:1905897"},{"relation_name":"regulates","term_name":"endoplasmic reticulum unfolded protein response","termid":"GO:0030968"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of endoplasmic reticulum unfolded protein response","synonyms":[{"name":"regulation of ER unfolded protein response","type":"exact"},{"name":"regulation of SREBP-mediated signalling pathway","type":"related"},{"name":"regulation of erUPR","type":"exact"}],"termid":"GO:1900101"}


id: PBO:0058618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6750","termid":"PBO:0058618"}


id: PBO:0049842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HEAT repeat containing 5A","termid":"PBO:0049842"}


id: PBO:0057464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 583","termid":"PBO:0057464"}


id: PBO:0000862
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.3.43","termid":"PBO:0000862"}


id: PBO:0073208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semaphorin 3G","termid":"PBO:0073208"}


id: PBO:0068370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 152 pseudogene 1","termid":"PBO:0068370"}


id: PBO:0068056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 361","termid":"PBO:0068056"}


id: PBO:0076989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THAP domain containing 5 pseudogene 2","termid":"PBO:0076989"}


id: PBO:0083416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the ORF PTC2/YER089C; identified by gene-trapping, expression analysis, and homology searching","termid":"PBO:0083416"}


id: PBO:0116302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Leucine-zipper transcriptional activator; regulates the sulfur amino acid pathway; requires different combinations of auxiliary factors Cbf1p, Met28p, Met31p and Met32p; specific involvement in sulfur starvation-induced autophagy with Gcn4p; feedforward loop exists in the regulation of genes controlled by Met4p and Met32p; ubiquitinated by SCF-Met30p, leading to either degradation or maintenance in an inactive state; regulates degradation of its DNA-binding cofactors by SCF-Met30p targeting","termid":"PBO:0116302"}


id: MONDO:0002935
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal cell carcinoma of the penis with an indolent clinical course. It is usually superficial and arises from the shaft and rarely the glans.","definition_xrefs":["NCIT:C39961"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"},{"relation_name":"is_a","term_name":"squamous cell carcinoma of penis","termid":"MONDO:0018352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"penis basal cell carcinoma","secondary_identifiers":["MEDGEN:275349","DOID:4277","UMLS:C1518949"],"synonyms":[{"name":"basal cell carcinoma of the penis","type":"exact"},{"name":"penile basal cell cancer","type":"exact"},{"name":"penile basal cell carcinoma","type":"exact"},{"name":"penis skin basal cell carcinoma","type":"exact"},{"name":"skin basal cell carcinoma of penis","type":"exact"},{"name":"skin of penis skin basal cell carcinoma","type":"exact"}],"termid":"MONDO:0002935","xrefs":{"Monarch":{"xref_id":"0002935"}}}


id: PBO:0001259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lid2 complex subunit Snt2","termid":"PBO:0001259"}


id: PBO:0086773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; SWAT-GFP and mCherry fusion proteins localize to the cell periphery","termid":"PBO:0086773"}


id: PBO:0084370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lipid raft associated protein; interacts with the plasma membrane ATPase Pma1p and has a role in its targeting to the plasma membrane by influencing its incorporation into lipid rafts; sometimes classified in the medium-chain dehydrogenase/reductases (MDRs) superfamily; AST1 has a paralog, AST2, that arose from the whole genome duplication","termid":"PBO:0084370"}


id: PBO:0082741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the RSC chromatin remodeling complex; essential gene required for cell cycle progression and maintenance of proper ploidy; phosphorylated in the G1 phase of the cell cycle; Snf5p paralog; hSNF5 tumor suppressor ortholog","termid":"PBO:0082741"}


id: GO:1901502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ether.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"ether metabolic process","termid":"GO:0018904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"ether catabolic process","synonyms":[{"name":"ether breakdown","type":"exact"},{"name":"ether catabolism","type":"exact"},{"name":"ether degradation","type":"exact"}],"termid":"GO:1901502"}


id: PBO:0082568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chaperone with a role in facilitating mitochondrial protein import; ascomycete-specific member of the DnaJ-like family, closely related to Ydj1p; predicted to be C-terminally prenylated; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0082568"}


id: MONDO:0044996
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease or disorder that involves the cerebral cortex.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral cortex disorder","secondary_identifiers":["MEDGEN:688117","SCTID:128128003","UMLS:C1263847"],"synonyms":[{"name":"cerebral cortex disease","type":"exact"},{"name":"cerebral cortex disease or disorder","type":"exact"},{"name":"disease of cerebral cortex","type":"exact"},{"name":"disease or disorder of cerebral cortex","type":"exact"},{"name":"disorder of cerebral cortex","type":"exact"}],"termid":"MONDO:0044996","xrefs":{"Monarch":{"xref_id":"0044996"}}}


id: PR:Q9UT21
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A developmentally-regulated GTP-binding protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11702:SF8","OMA:SCHPO00593","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized GTP-binding protein C9.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9.07c","secondary_identifiers":["UniProtKB:Q9UT21"],"synonyms":[{"name":"Spom972h-DRG1","type":"exact"}],"termid":"PR:Q9UT21"}


id: GO:2000290
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of myotome development.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"myotome development","termid":"GO:0061055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of myotome development","termid":"GO:2000290"}


id: PBO:0114421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arachidonate epidermal lipoxygenase 3","termid":"PBO:0114421"}


id: PBO:0080573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat containing planar cell polarity effector","termid":"PBO:0080573"}


id: PBO:0028606
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_pyrithiamine","termid":"PBO:0028606"}


id: GO:0034515
data:
  {"annotated_genes":["SJAG_03638","SJAG_02900","SJAG_04088"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73454,80200,96732],"is_not":false,"summary":null,"term":"GO:0034515"}]},"cv_name":"cellular_component","definition":"An aggregation of proteasome core protease (CP) and regulatory particle (RP) complexes that localizes in the cytoplasm as dot-like structures when cells are in a quiescent state.","definition_xrefs":["GOC:rb","PMID:18504300","GOC:krc","PMID:30204036"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02900":null,"SJAG_03638":null,"SJAG_04088":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"proteasome storage granule","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"PSG","type":"related"}],"termid":"GO:0034515","terms_by_termid":{"GO:0034515":null}}


id: MONDO:0002373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign proliferative neoplasm made up of epithelial and mesenchymal cells of the mesothelium which make up part of the serosal covering and lining of various organ surfaces within the body.","definition_xrefs":["PMID:30285380"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesothelioma","termid":"MONDO:0005065"},{"relation_name":"is_a","term_name":"benign neoplasm","termid":"MONDO:0005165"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign mesothelioma","secondary_identifiers":["UMLS:C0348424","ICD10CM:C45","SCTID:254825007","DOID:2645","MESH:D008654","NCIT:C3234","MEDGEN:578420","ICD9:215.9"],"synonyms":[{"name":"benign tumor of mesothelial tissue","type":"exact"},{"name":"benign tumor of mesothelium","type":"exact"},{"name":"benign tumour of mesothelial tissue","type":"exact"},{"name":"benign tumour of mesothelium","type":"exact"},{"name":"mesothelioma, benign","type":"exact"}],"termid":"MONDO:0002373","xrefs":{"Monarch":{"xref_id":"0002373"}}}


id: PATO:0002537
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spheroid quality inhering in a bearer by virtue of the bearer's exhibiting a shape not quite ovoid. approximately ovoid.","definition_xrefs":["merriam-webster:http://www.merriam-webster.com/dictionary/subovoid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spheroid","termid":"PATO:0001865"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subovoid","termid":"PATO:0002537"}


id: GO:0098666
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that is capable of G protein-coupled serotonin receptor activity.","definition_xrefs":["GOC:TermGenie","GOC:bhm","GO_REF:0000088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor complex","termid":"GO:0043235"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"G protein-coupled serotonin receptor complex","synonyms":[{"name":"G-protein coupled serotonin receptor complex","type":"exact"}],"termid":"GO:0098666"}


id: SO:0000211
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding alanyl tRNA.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanine_tRNA_primary_transcript","synonyms":[{"name":"alanine tRNA primary transcript","type":"exact"}],"termid":"SO:0000211"}


id: PBO:0073011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sodium voltage-gated channel alpha subunit 11","termid":"PBO:0073011"}


id: PBO:0057136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 218-1","termid":"PBO:0057136"}


id: GO:0009951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process resulting in the establishment of polarity along the dorsal/ventral axis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of axis polarity","termid":"GO:0065001"},{"relation_name":"part_of","term_name":"dorsal/ventral axis specification","termid":"GO:0009950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"polarity specification of dorsal/ventral axis","synonyms":[{"name":"polarity specification of dorsal-ventral axis","type":"exact"},{"name":"polarity specification of dorsoventral axis","type":"exact"}],"termid":"GO:0009951"}


id: PBO:0074876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 58A","termid":"PBO:0074876"}


id: GO:0050878
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the levels of body fluids.","definition_xrefs":["GOC:tb","GOC:ai","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of body fluid levels","termid":"GO:0050878"}


id: PBO:0026968
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_swollen_pear-shaped_vegetative_cell","termid":"PBO:0026968"}


id: FYPO:0006094
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the assembly of actin filament bundles is abnormal.","definition_xrefs":["PomBase:mah","GO:0061572"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular component assembly during vegetative growth","termid":"FYPO:0001354"},{"relation_name":"is_a","term_name":"abnormal actin filament bundle organization","termid":"FYPO:0005979"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0004803","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abnormal actin filament bundle assembly","synonyms":[{"name":"abnormal actin bundling","type":"exact"},{"name":"abnormal actin filament bundle assembly during mitotic cell cycle","type":"related"},{"name":"abnormal actin filament bundle assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0006094"}


id: MONDO:0100522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Marie Unna hereditary hypotrichosis","termid":"MONDO:0018631"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis 4","secondary_identifiers":["OMIM:146550","MEDGEN:413053","UMLS:C2750815","DOID:0110701","GARD:15078","MESH:C567718"],"synonyms":[{"name":"HYPT4","type":"exact"},{"name":"MUHH1","type":"exact"},{"name":"Marie Unna hereditary hypotrichosis 1","type":"exact"},{"name":"hypotrichosis 4","type":"exact"},{"name":"hypotrichosis type 4","type":"exact"},{"name":"hypotrichosis, Marie Unna type, 1","type":"exact"}],"termid":"MONDO:0100522","xrefs":{"Monarch":{"xref_id":"0100522"}}}


id: GO:0044494
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism initiates, promotes, or enhances the activity of a voltage-gated sodium channel in another organism via the action of a venom.","definition_xrefs":["GOC:jl","PMID:21781281","GOC:fj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of voltage-gated sodium channel activity","termid":"GO:0044492"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"venom-mediated activation of voltage-gated sodium channel activity","synonyms":[{"name":"envenomation resulting in positive regulation of voltage-gated sodium channel activity in another organism","type":"exact"},{"name":"envenomation resulting in positive regulation of voltage-gated sodium channel activity in other organism","type":"exact"}],"termid":"GO:0044494"}


id: PBO:0051900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit alpha 8","termid":"PBO:0051900"}


id: MONDO:0007440
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"bipolar I disorder","termid":"MONDO:0001866"},{"relation_name":"is_a","term_name":"bipolar disorder","termid":"MONDO:0004985"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major affective disorder 1","secondary_identifiers":["MEDGEN:377615","OMIM:125480","MESH:C565111","DOID:0080220","UMLS:C1852197"],"synonyms":[{"name":"MAFD1","type":"exact"},{"name":"MAJOR affective disorder 1","type":"related"},{"name":"bipolar affective disorder","type":"related"},{"name":"major affective disorder 1","type":"exact"},{"name":"manic-depressive psychosis","type":"related"},{"name":"manic-depressive psychosis, autosomal","type":"related"}],"termid":"MONDO:0007440","xrefs":{"Monarch":{"xref_id":"0007440"}}}


id: PBO:0058146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4442","termid":"PBO:0058146"}


id: MONDO:0018934
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mucopolysaccharidosis type 1 (obsolete MONDO:0018934)","termid":"MONDO:0018934","xrefs":{"Monarch":{"xref_id":"0018934"}}}


id: FYPO:0001381
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a protein kinase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652","FYPO:0000654","FYPO:0000707","FYPO:0000661"],"is_obsolete":false,"name":"abnormal protein kinase activity","termid":"FYPO:0001381"}


id: GO:0019597
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of (R)-mandelate into other compounds, including benzoate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benzoate metabolic process","termid":"GO:0018874"},{"relation_name":"is_a","term_name":"mandelate catabolic process","termid":"GO:0019596"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"(R)-mandelate catabolic process to benzoate","synonyms":[{"name":"(R)-mandelate breakdown to benzoate","type":"exact"},{"name":"(R)-mandelate degradation to benzoate","type":"exact"}],"termid":"GO:0019597"}


id: PBO:0060825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NECTIN1 divergent transcript","termid":"PBO:0060825"}


id: PBO:0057928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3654","termid":"PBO:0057928"}


id: GO:0090186
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of pancreatic juice secretion, the regulated release of pancreatic juice by the exocrine pancreas into the upper part of the intestine.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of digestive system process","termid":"GO:0044058"},{"relation_name":"is_a","term_name":"regulation of body fluid levels","termid":"GO:0050878"},{"relation_name":"is_a","term_name":"regulation of secretion","termid":"GO:0051046"},{"relation_name":"regulates","term_name":"pancreatic juice secretion","termid":"GO:0030157"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of pancreatic juice secretion","termid":"GO:0090186"}


id: GO:0005518
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to collagen, a group of fibrous proteins of very high tensile strength that form the main component of connective tissue in animals. Collagen is highly enriched in glycine (some regions are 33% glycine) and proline, occurring predominantly as 3-hydroxyproline (about 20%).","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"collagen binding","termid":"GO:0005518"}


id: PBO:0056244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"magnesium transporter 1","termid":"PBO:0056244"}


id: PBO:0005908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar amino acid uptake transporter (predicted)","termid":"PBO:0005908"}


id: PBO:0072774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serum amyloid A3, pseudogene","termid":"PBO:0072774"}


id: PBO:0061065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sodium/potassium transporting ATPase interacting 4","termid":"PBO:0061065"}


id: PBO:0066979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 282","termid":"PBO:0066979"}


id: FYPO:0008066
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the mitotic cell cycle is no longer arrested during G1 phase when phosphate is removed. Arrest may either occur under conditions where arrest is not a normal occurrence, or may progress differently from normal under conditions where arrest normally does take place.","definition_xrefs":["PMID:36779416"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell cycle arrest in mitotic G1 phase","termid":"FYPO:0005097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished cell cycle arrest in mitotic G1 phase in response to phosphate starvation","termid":"FYPO:0008066"}


id: PBO:0065065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteoglycan 3, pro eosinophil major basic protein 2","termid":"PBO:0065065"}


id: GO:0006233
data:
  {"annotated_genes":["SJAG_04657"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71368],"is_not":false,"summary":null,"term":"GO:0006233"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dTDP, deoxyribosylthymine diphosphate (2'-deoxyribosylthymine5'-diphosphate).","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside diphosphate biosynthetic process","termid":"GO:0009197"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleotide biosynthetic process","termid":"GO:0009221"},{"relation_name":"is_a","term_name":"dTDP metabolic process","termid":"GO:0046072"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04657":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"dTDP biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"dTDP anabolism","type":"exact"},{"name":"dTDP biosynthesis","type":"exact"},{"name":"dTDP formation","type":"exact"},{"name":"dTDP synthesis","type":"exact"}],"termid":"GO:0006233","terms_by_termid":{"GO:0006233":null}}


id: PBO:0002225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis CGR1 family (predicted)","termid":"PBO:0002225"}


id: SO:0100015
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The more polar, carboxy-terminal region of the signal peptide (approx 3-7 aa).","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleaved_peptide_region","termid":"SO:0100011"},{"relation_name":"part_of","term_name":"signal_peptide","termid":"SO:0000418"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"c_terminal_region","synonyms":[{"name":"C-region","type":"related"}],"termid":"SO:0100015"}


id: PR:Q9UTD3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein YIPF1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00197"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein YIP5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC227.06","secondary_identifiers":["UniProtKB:Q9UTD3"],"synonyms":[{"name":"Spom972h-YIPF1","type":"exact"},{"name":"YPT-interacting protein 5 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTD3"}


id: GO:0047633
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: agmatine + ATP = N(4)-phosphoagmatine + ADP + 3 H+.","definition_xrefs":["EC:2.7.3.10","RHEA:15953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, nitrogenous group as acceptor","termid":"GO:0016775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"agmatine kinase activity","secondary_identifiers":["MetaCyc:AGMATINE-KINASE-RXN","KEGG_REACTION:R01417"],"synonyms":[{"name":"ATP:agmatine 4-N-phosphotransferase activity","type":"related"},{"name":"ATP:agmatine N4-phosphotransferase activity","type":"related"},{"name":"phosphagen phosphokinase activity","type":"related"}],"termid":"GO:0047633"}


id: MONDO:0032649
data:
  {"annotated_genes":["SJAG_00624"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86616],"is_not":false,"summary":null,"term":"MONDO:0032649"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypotrichosis","termid":"MONDO:0003037"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00624":null},"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis 14","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16335","DOID:0080582","MEDGEN:1648477","OMIM:618275","UMLS:C4748930"],"synonyms":[{"name":"HYPOTRICHOSIS 14","type":"related"},{"name":"HYPT14","type":"related"}],"termid":"MONDO:0032649","terms_by_termid":{"MONDO:0032649":null},"xrefs":{"Monarch":{"xref_id":"0032649"}}}


id: PBO:0077491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 212","termid":"PBO:0077491"}


id: PBO:0086156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for pre-rRNA processing; associated with the 90S pre-ribosome and 43S small ribosomal subunit precursor; interacts with U3 snoRNA; binds G-quadruplex (G4) structures in DNA; deletion mutant has synthetic fitness defect with an sgs1 deletion mutant","termid":"PBO:0086156"}


id: PBO:0053498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 477","termid":"PBO:0053498"}


id: PBO:0077452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM183A pseudogene 2","termid":"PBO:0077452"}


id: PBO:0059143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannose phosphate isomerase","termid":"PBO:0059143"}


id: GO:0044520
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant positive regulation of the activity of a vasoactive intestinal polypeptide receptor in the bitten organism.","definition_xrefs":["GOC:jl","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete envenomation resulting in positive regulation of vasoactive intestinal polypeptide receptor activity in another organism (obsolete GO:0044520)","synonyms":[{"name":"envenomation resulting in positive regulation of VIP receptor activity in other organism","type":"exact"},{"name":"envenomation resulting in positive regulation of vasoactive intestinal polypeptide receptor activity in other organism","type":"exact"}],"termid":"GO:0044520"}


id: PATO:0000914
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000914 continuant (obsolete PATO:0000914)","termid":"PATO:0000914"}


id: PR:000044504
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GTP-binding protein ypt5 (Schizosaccharomyces pombe) that is prenylated with Geranylgeranyl moieties on the Cys residues within the CxC motif. Example: UniProtKB:P36586-1, Cys-209/Cys-211, MOD:00113.","definition_xrefs":["PMID:1597466","PomBase:MAH","PMID:8226998"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GTP-binding protein ypt5 (Schizosaccharomyces pombe)","termid":"PR:000030005"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ypt5/Ip(C209,C211)","pombase_gene_id":"SPAC6F6.15","synonyms":[{"name":"PomBase_original_PRO_term_name: GTP-binding protein ypt5 prenylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"SpYPT5p prenylated","type":"related"},{"name":"ypt5/Ip(C209,C211)","type":"exact"}],"termid":"PR:000044504"}


id: PBO:0089472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WIP family cytoskeletal protein Bbc1","termid":"PBO:0089472"}


id: MONDO:0005140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm originating from the surface ovarian epithelium. It accounts for the greatest number of deaths from malignancies of the female genital tract and is the fifth leading cause of cancer fatalities in women. It is predominantly a disease of older white women of northern European extraction, but it is seen in all ages and ethnic groups. Adenocarcinomas constitute the vast majority of ovarian carcinomas. The pattern of metastatic spread in ovarian carcinoma is similar regardless of the microscopic type. The most common sites of involvement are the contralateral ovary, peritoneal cavity, para-aortic and pelvic lymph nodes, and liver. Lung and pleura are the most common sites of extra-abdominal spread. The primary form of therapy is surgical. The overall prognosis of ovarian carcinoma remains poor, a direct result of its rapid growth rate and the lack of early symptoms. --2002","definition_xrefs":["NCIT:C4908"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant epithelial tumor of ovary","termid":"MONDO:0018364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"ovarian carcinoma","secondary_identifiers":["UMLS:C4721610","DOID:4001","EFO:0001075","MEDGEN:1648335"],"synonyms":[{"name":"carcinoma of ovary","type":"exact"},{"name":"carcinoma of the ovary","type":"exact"},{"name":"epithelial ovarian cancer","type":"exact"},{"name":"ovarian cancer","type":"broad"},{"name":"ovarian carcinoma","type":"exact"},{"name":"ovarian epithelial cancer","type":"broad"},{"name":"ovary carcinoma","type":"exact"}],"termid":"MONDO:0005140","xrefs":{"Monarch":{"xref_id":"0005140"}}}


id: GO:0035299
data:
  {"annotated_genes":["SJAG_01148"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75144],"is_not":false,"summary":null,"term":"GO:0035299"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1,3,4,5,6-pentakisphosphate + ATP = 1D-myo-inositol hexakisphosphate + ADP + H+.","definition_xrefs":["RHEA:20313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol pentakisphosphate kinase activity","termid":"GO:0120517"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01148":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016301","GO:0003824"],"is_obsolete":false,"name":"inositol-1,3,4,5,6-pentakisphosphate 2-kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R05202","EC:2.7.1.158","Reactome:R-HSA-1855176","MetaCyc:RXN-7163","Reactome:R-HSA-1855179"],"synonyms":[{"name":"IP5 2-kinase activity","type":"related"},{"name":"Ins(1,3,4,5,6)P5 2-kinase activity","type":"related"},{"name":"inositol hexakisphosphate synthase","type":"related"},{"name":"inositol pentakisphosphate 2-kinase activity","type":"exact"},{"name":"inositol polyphosphate kinase activity","type":"related"},{"name":"inositol-pentakisphosphate 2-kinase activity","type":"related"}],"termid":"GO:0035299","terms_by_termid":{"GO:0035299":null}}


id: PR:Q02061
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerase II subunit RPB2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00333","PANTHER:PTHR20856:SF7","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase II subunit RPB2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23G3.01","secondary_identifiers":["UniProtKB:Q02061"],"synonyms":[{"name":"DNA-directed RNA polymerase II 138 kDa polypeptide (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerase II subunit 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerase II subunit B2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-POLR2B","type":"exact"}],"termid":"PR:Q02061"}


id: GO:1900631
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving tridecane.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkane metabolic process","termid":"GO:0043446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"tridecane metabolic process","synonyms":[{"name":"tridecane metabolism","type":"exact"}],"termid":"GO:1900631"}


id: PBO:0038953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adiponectin receptor 1","termid":"PBO:0038953"}


id: PBO:0040247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy related 4B cysteine peptidase","termid":"PBO:0040247"}


id: GO:1990794
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of a cell situated by the cell sides which interface adjacent cells and near the base. Often used in reference to animal polarized epithelial cells.","definition_xrefs":["PMID:18495799"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"basal part of cell","termid":"GO:0045178"},{"relation_name":"part_of","term_name":"lateral part of cell","termid":"GO:0097574"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"basolateral part of cell","termid":"GO:1990794"}


id: PBO:0087232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sensor of mitochondrial dysfunction; regulates the subcellular location of Rtg1p and Rtg3p, transcriptional activators of the retrograde (RTG) and TOR pathways; Rtg2p is inhibited by the phosphorylated form of Mks1p","termid":"PBO:0087232"}


id: GO:0052141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism towards a higher concentration of a specific chemical on or near its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive chemotaxis on or near host (obsolete GO:0052141)","termid":"GO:0052141"}


id: PBO:0052612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KRAB box domain containing 4","termid":"PBO:0052612"}


id: MONDO:1012381
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial thoracic aortic aneurysm, non-human animal","termid":"MONDO:1011648"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial thoracic aortic aneurysm, dog","secondary_identifiers":["OMIA:001419-9615"],"termid":"MONDO:1012381","xrefs":{"Monarch":{"xref_id":"1012381"}}}


id: PBO:0045045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dickkopf like acrosomal protein 1","termid":"PBO:0045045"}


id: PBO:0055211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2636","termid":"PBO:0055211"}


id: GO:0033877
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-2-benzylsuccinate + succinyl-CoA = (R)-2-benzylsuccinyl-CoA + succinate.","definition_xrefs":["RHEA:16469","EC:2.8.3.15"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-transferase activity","termid":"GO:0008410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016782"],"is_obsolete":false,"name":"succinyl-CoA:(R)-benzylsuccinate CoA-transferase activity","secondary_identifiers":["KEGG_REACTION:R05588","MetaCyc:RXN-864","GO:0018728","UM-BBD_reactionID:r0329"],"synonyms":[{"name":"benzylsuccinate CoA-transferase activity","type":"related"},{"name":"succinyl-CoA:(R)-2-benzylsuccinate CoA-transferase activity","type":"related"},{"name":"succinyl-CoA:benzylsuccinate CoA-transferase activity","type":"exact"}],"termid":"GO:0033877"}


id: GO:0170016
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together an endosome and an ER membrane either via membrane lipid binding or by interacting with an endosome protein, to establish and facilitate organelle exchange.","definition_xrefs":["PMID:33124732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum-organelle membrane tether activity","termid":"GO:0170009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030674"}],"interesting_parent_ids":["GO:0030674","GO:0003674","GO:0060090"],"is_obsolete":false,"name":"endoplasmic reticulum-endosome tether activity","termid":"GO:0170016"}


id: PR:O94404
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A NIF3-like protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13799:SF13","PRO:DNx","OMA:SCHPO04957"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein NIF3 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC126.12","secondary_identifiers":["UniProtKB:O94404"],"synonyms":[{"name":"Spom972h-NIF3L1","type":"exact"}],"termid":"PR:O94404"}


id: PBO:0005034
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.8.1.6","termid":"PBO:0005034"}


id: PBO:0081830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 764","termid":"PBO:0081830"}


id: PBO:0078794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (GTT) 16-1","termid":"PBO:0078794"}


id: PBO:0072756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S100A11 pseudogene 6","termid":"PBO:0072756"}


id: PBO:0044582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"drebrin 1","termid":"PBO:0044582"}


id: PBO:0047311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fas activated serine/threonine kinase","termid":"PBO:0047311"}


id: PBO:0055885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 8 VRAC subunit C","termid":"PBO:0055885"}


id: PBO:0057402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548h-4","termid":"PBO:0057402"}


id: PBO:0003765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase I complex subunit Rpa34 (predicted)","termid":"PBO:0003765"}


id: PBO:0067725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 23","termid":"PBO:0067725"}


id: PBO:0031678
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_cell_cycle_arrest_in_response_to_pheromone","termid":"PBO:0031678"}


id: PBO:0028700
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_RNA_catabolic_process","termid":"PBO:0028700"}


id: SO:0001685
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The score of an experimentally derived feature such as a p-value.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"experimental_feature_attribute","termid":"SO:0001684"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"score","termid":"SO:0001685"}


id: PBO:0029923
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-GGPP_absent_from_cell","termid":"PBO:0029923"}


id: MONDO:0013840
data:
  {"annotated_genes":["SJAG_01866"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86649],"is_not":false,"summary":null,"term":"MONDO:0013840"}]},"cv_name":"mondo","definition":"Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome is a rare mitochondrial disease due to a defect in coenzyme Q10 biosynthesis that manifests with a broad spectrum of signs and symptoms which may include: neonatal lactic acidosis, global developmental delay, tonus disorder, seizures, reduced spontaneous movements, ventricular hypertrophy, bradycardia, renal tubular dysfunction with massive lactic acid excretion in urine, severe biochemical defect of respiratory chain complexes II/III when assayed together and deficiency of coenzyme Q10 in skeletal muscle. Cerebral and cerebellar atrophy can be seen on magnetic resonance imaging and multiple choroid plexus cysts and symmetrical hyperechoic signal alterations in basal ganglia have been observed on ultrasound.","definition_xrefs":["Orphanet:319678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coenzyme Q10 deficiency","termid":"MONDO:0018151"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01866":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069","MONDO:0005244"],"is_obsolete":false,"name":"encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:614654","UMLS:C3553374","DOID:0070242","GARD:17470","MEDGEN:766288"],"synonyms":[{"name":"COQ10D5","type":"related"},{"name":"coenzyme Q10 deficiency, primary, 5","type":"related"},{"name":"coenzyme Q10 deficiency, primary, type 5","type":"exact"}],"termid":"MONDO:0013840","terms_by_termid":{"MONDO:0013840":null},"xrefs":{"Monarch":{"xref_id":"0013840"}}}


id: PBO:0089404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA (uridine) methyltransferase Trm9","termid":"PBO:0089404"}


id: MONDO:0001909
data:
  {"annotated_genes":["SJAG_00516","SJAG_01183"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85845],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011422"},{"annotations":[86490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011268"}]},"cv_name":"mondo","definition":"A group of genetic disorders of the kidney tubules characterized by the accumulation of metabolically produced acids with elevated plasma chloride, hyperchloremic metabolic acidosis. Defective renal acidification of urine (proximal tubules) or low renal acid excretion (distal tubules) can lead to complications such as hypokalemia, hypercalcinuria with nephrolithiasis and nephrocalcinosis, and rickets.","definition_xrefs":["MESH:D000141"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acidosis disorder","termid":"MONDO:0006022"},{"relation_name":"is_a","term_name":"renal tubular transport disease","termid":"MONDO:0006510"},{"relation_name":"is_a","term_name":"renal tubule disorder","termid":"MONDO:0021568"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00516":null,"SJAG_01183":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005240"],"is_obsolete":false,"name":"renal tubular acidosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:588.89","UMLS:C0001126","DOID:14219","MEDGEN:90","NANDO:2100019","NANDO:2200144","GARD:7552","icd11.foundation:1272869150","SCTID:1776003"],"termid":"MONDO:0001909","terms_by_termid":{"MONDO:0011268":null,"MONDO:0011422":null},"xrefs":{"Monarch":{"xref_id":"0001909"}}}


id: PBO:0000754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor Spt5","termid":"PBO:0000754"}


id: PBO:0041541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 17 open reading frame 99","termid":"PBO:0041541"}


id: FYPO:0002908
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription occurs to a greater extent than normal in telomeric regions. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription during vegetative growth","termid":"FYPO:0000780"},{"relation_name":"is_a","term_name":"abnormal transcription at telomere","termid":"FYPO:0007420"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000294","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased transcription at telomere during vegetative growth","synonyms":[{"name":"increased telomeric transcription during vegetative growth","type":"exact"},{"name":"increased transcription at telomere during mitotic cell cycle","type":"related"},{"name":"increased transcription from telomere during vegetative growth","type":"exact"}],"termid":"FYPO:0002908"}


id: PBO:0046706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ETS variant transcription factor 5","termid":"PBO:0046706"}


id: GO:0006941
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within striated muscle tissue, resulting in the shortening of the muscle. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis. Striated muscle is a type of muscle in which the repeating units (sarcomeres) of the contractile myofibrils are arranged in registry throughout the cell, resulting in transverse or oblique striations observable at the level of the light microscope.","definition_xrefs":["GOC:jl","GOC:mtg_muscle","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle contraction","termid":"GO:0006936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"striated muscle contraction","synonyms":[{"name":"sarcomeric muscle contraction","type":"exact"}],"termid":"GO:0006941"}


id: MONDO:1011266
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cone-rod dystrophy that occurs in dogs due to a mutation in the PDE6B gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy, non-human animal","termid":"MONDO:1012582"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cone-rod dystrophy, PDE6B-related dog","secondary_identifiers":["OMIA:001674-9615"],"synonyms":[{"name":"retinal atrophy - cone-rod dystrophy 1, dog","type":"related"}],"termid":"MONDO:1011266","xrefs":{"Monarch":{"xref_id":"1011266"}}}


id: PBO:0086022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; the authentic protein is detected in highly purified mitochondria in high-throughput studies; null mutant displays reduced frequency of mitochondrial genome loss","termid":"PBO:0086022"}


id: MONDO:0006701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epithelial neoplasm of the anterior pituitary gland in which the neoplastic cells do not stain with acidic or basic dyes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pituitary gland adenoma","termid":"MONDO:0006373"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromophobe adenoma","secondary_identifiers":["DOID:3828","EFO:1000867","ICDO:8270/0","MEDGEN:1747","MESH:D000238","UMLS:C0001432","NCIT:C2857"],"synonyms":[{"name":"chromophobe adenoma of pituitary gland","type":"exact"},{"name":"chromophobe adenoma of the pituitary gland","type":"exact"},{"name":"pituitary chromophobe adenoma","type":"exact"},{"name":"pituitary gland chromophobe adenoma","type":"exact"}],"termid":"MONDO:0006701","xrefs":{"Monarch":{"xref_id":"0006701"}}}


id: MOD:00712
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-proline residue to a methylated proline, such as N,N-dimethylproline.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"methylated proline","synonyms":[{"name":"MePro","type":"exact"}],"termid":"MOD:00712"}


id: PBO:0068904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 146, pseudogene","termid":"PBO:0068904"}


id: RO:0009003
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"\\\"immersed in\\\" is a relation between a (physical) entity and a fluid substance in which the entity is wholely or substantially surrounded by the substance.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immersed_in","termid":"RO:0009003"}


id: GO:0036101
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of leukotriene B4, a leukotriene composed of (6Z,8E,10E,14Z)-eicosatetraenoic acid having (5S)- and (12R)-hydroxy substituents.","definition_xrefs":["GOC:yaf","PMID:9799565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukotriene catabolic process","termid":"GO:0036100"},{"relation_name":"is_a","term_name":"leukotriene B4 metabolic process","termid":"GO:0036102"},{"relation_name":"is_a","term_name":"long-chain fatty acid catabolic process","termid":"GO:0042758"},{"relation_name":"is_a","term_name":"icosanoid catabolic process","termid":"GO:1901523"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"leukotriene B4 catabolic process","synonyms":[{"name":"LTB4 catabolism","type":"exact"},{"name":"leukotriene B4 breakdown","type":"exact"},{"name":"leukotriene B4 catabolism","type":"exact"},{"name":"leukotriene B4 degradation","type":"exact"}],"termid":"GO:0036101"}


id: PBO:0077045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid hormone receptor associated protein 3","termid":"PBO:0077045"}


id: PBO:0026749
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_torin1","termid":"PBO:0026749"}


id: PBO:0076177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 1E member 1","termid":"PBO:0076177"}


id: GO:0085042
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A host-derived membrane surrounding the symbiont arbuscule during symbiosis.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell membrane","termid":"GO:0033644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"periarbuscular membrane","termid":"GO:0085042"}


id: MONDO:0021805
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acromesomelic dysplasia","termid":"MONDO:0019696"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"acromesomelic dysplasia, Campailla Martinelli type","secondary_identifiers":["UMLS:C2930969","GARD:505","MEDGEN:418955","MESH:C535659"],"synonyms":[{"name":"acromesomelic dysplasia Campailla Martinelli type","type":"related"},{"name":"mesomelic dwarfism Campailla-Martinelli type","type":"related"}],"termid":"MONDO:0021805","xrefs":{"Monarch":{"xref_id":"0021805"}}}


id: PR:O14067
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1687.08 gene.","definition_xrefs":["UniProtKB:O14067","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1687.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.08","synonyms":[{"name":"Spom972h-SPAC1687.08","type":"exact"}],"termid":"PR:O14067"}


id: PBO:0044289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome X open reading frame 58","termid":"PBO:0044289"}


id: PBO:0064536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase mitochondrial pseudogene 1","termid":"PBO:0064536"}


id: MONDO:0043459
data:
  {"annotated_genes":["SJAG_00995","SJAG_03206","SJAG_01207"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011125"},{"annotations":[85647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014615"},{"annotations":[85648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014619"}]},"cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder which results from exposure to radiation. Examples of non-neoplastic disorders include dermatitis, enteritis, stomatitis, pneumonitis, and cerebritis. Examples of neoplastic disorders include myelodysplastic syndromes, leukemias, and sarcomas.","definition_xrefs":["NCIT:C26684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00995":null,"SJAG_01207":null,"SJAG_03206":null},"genotype_count":0,"is_obsolete":false,"name":"radiation-induced disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0009565","MEDGEN:734320","Orphanet:521132","GARD:22139","SCTID:85983004","UMLS:C1527225","MESH:D000016"],"synonyms":[{"name":"Abnormality, radiation-induced","type":"related"},{"name":"abnormalities, radiation induced","type":"related"},{"name":"radiation induced abnormalities","type":"related"},{"name":"radiation-induced Abnormality","type":"exact"},{"name":"radiation-induced abnormalities","type":"exact"},{"name":"radiation-induced disorder","type":"exact"}],"termid":"MONDO:0043459","terms_by_termid":{"MONDO:0011125":null,"MONDO:0014615":null,"MONDO:0014619":null},"xrefs":{"Monarch":{"xref_id":"0043459"}}}


id: MONDO:0017767
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A post-bacterial multisystem inflammatory disease occurring as a post-infectious, nonsuppurative sequela of untreated streptococcus pyogenes (Group A streptococcus [GAS]) pharyngitis, and mainly occurs in individuals aged 5 to 15 years. The most common presenting signs are fever, migratory polyarthritis and carditis.","definition_xrefs":["Orphanet:3099"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"connective tissue disorder","termid":"MONDO:0003900"},{"relation_name":"excluded_subClassOf","term_name":"bacterial infectious disease","termid":"MONDO:0005113"},{"relation_name":"excluded_subClassOf","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"rheumatic disorder","termid":"MONDO:0005554"},{"relation_name":"is_a","term_name":"post-bacterial disorder","termid":"MONDO:0021673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rheumatic fever","secondary_identifiers":["DOID:1586","NCIT:C34984","NORD:1668","SCTID:81077008","GARD:5699","ICD9:390","MedDRA:10039054","ICD10CM:I00-I02","EFO:1001160","ICD9:390-392.99","MESH:D012213","SCTID:58718002","MEDGEN:48448","UMLS:C0035436"],"synonyms":[{"name":"ARF","type":"exact"},{"name":"RHF - rheumatic fever","type":"exact"},{"name":"acute rheumatic fever","type":"exact"},{"name":"inflammatory rheumatism","type":"related"}],"termid":"MONDO:0017767","xrefs":{"Monarch":{"xref_id":"0017767"}}}


id: PBO:0046772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exophilin 5","termid":"PBO:0046772"}


id: PBO:0017015
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Orc4 binding footprint at replication origins is extended in G1 in the presence of Cdc1 and the MCM complex","termid":"PBO:0017015"}


id: PBO:0090411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterochromatin (HP1) family chromodomain protein Chp1","termid":"PBO:0090411"}


id: MOD:00893
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Natural or modified residues with a mass of 128.0-128.1 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at a resolution below 0.1 Da","termid":"MOD:00616"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"residues isobaric at 128.0-128.1","termid":"MOD:00893"}


id: FYPO:0002912
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an inviable cell that does not divide, is elongated, and contains more than one nucleus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated multinucleate vegetative cell","termid":"FYPO:0001493"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, elongated cell","termid":"FYPO:0004603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0001320","FYPO:0001985","FYPO:0000004","FYPO:0000002","FYPO:0005447","FYPO:0000005","FYPO:0000631"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, elongated multinucleate cell","synonyms":[{"name":"inviable after spore germination, multinucleate elongated cell","type":"exact"},{"name":"inviable after spore germination, undivided elongated multinucleate cell","type":"exact"},{"name":"inviable following spore germination, without cell division, elongated multinucleate cell","type":"exact"},{"name":"inviable germinated spore, without cell division, elongated multinucleate cell","type":"exact"},{"name":"lethal after spore germination, without cell division, elongated multinucleate cell","type":"exact"}],"termid":"FYPO:0002912"}


id: GO:0014864
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a muscle activity stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to muscle activity","termid":"GO:0014850"},{"relation_name":"is_a","term_name":"detection of activity","termid":"GO:0014865"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of muscle activity","termid":"GO:0014864"}


id: PBO:0069554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 826, pseudogene","termid":"PBO:0069554"}


id: PBO:0082259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Amidase; removes the amide group from N-terminal asparagine and glutamine residues to generate proteins with N-terminal aspartate and glutamate residues that are targets of ubiquitin-mediated degradation","termid":"PBO:0082259"}


id: GO:0043582
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the sporangium over time, from its formation to the mature structure. A sporangium is a structure producing and containing spores.","definition_xrefs":["Wikipedia:Sporagium","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spore-bearing structure development","termid":"GO:0075259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"sporangium development","synonyms":[{"name":"sporangia development","type":"exact"}],"termid":"GO:0043582"}


id: GO:0070707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of an RNA molecule by insertion of a dinucleotide.","definition_xrefs":["GOC:mah","GOC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA nucleotide insertion","termid":"GO:0070705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"RNA dinucleotide insertion","termid":"GO:0070707"}


id: RO:0002460
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"is_vector_for","termid":"RO:0002459"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_vector","termid":"RO:0002460"}


id: PBO:0071940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4X pseudogene 17","termid":"PBO:0071940"}


id: MONDO:0015683
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary malignant peritoneal tumor (obsolete MONDO:0015683)","secondary_identifiers":["Orphanet:168807"],"termid":"MONDO:0015683","xrefs":{"Monarch":{"xref_id":"0015683"}}}


id: GO:0102814
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: delphinidin 3,3',5-tri-O-beta-D-glucoside betaine + caffeoyl-CoA = delphinidin 3-O-glucosyl-5-O-(caffeoylglucoside-3'-O-glucoside) + coenzyme A.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete caffeoyl-CoA:delphinidin-3,5,3'-triglucoside 5-O-glucoside-6-O-hydroxycinnamoyltransferase activity (obsolete GO:0102814)","termid":"GO:0102814"}


id: PBO:0072107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S13 pseudogene 5","termid":"PBO:0072107"}


id: GO:0046572
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: versiconal = versicolorin B + H2O.","definition_xrefs":["PMID:8784203","MetaCyc:RXN-9494"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity","termid":"GO:0016835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"versicolorin B synthase activity","secondary_identifiers":["EC:4.2.1.143","RHEA:33859"],"termid":"GO:0046572"}


id: MONDO:0007986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Metatropic dysplasia (MTD) is a rare spondyloepimetaphyseal dysplasia characterized by a long trunk and short limbs in infancy followed by severe and progressive kyphoscoliosis causing a reversal in proportions during childhood (short trunk and long limbs) and a final short stature in adulthood.","definition_xrefs":["Orphanet:2635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"},{"relation_name":"is_a","term_name":"TRPV4-related bone disorder","termid":"MONDO:0018240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"metatropic dysplasia","secondary_identifiers":["NORD:1445","MEDGEN:82699","UMLS:C0265281","DOID:0111514","MESH:C537356","GARD:3571","NCIT:C175209","OMIM:156530","SCTID:22764001"],"synonyms":[{"name":"Metatropic Dysplasia I","type":"exact"},{"name":"Metatropic dwarfism","type":"exact"},{"name":"Metatropic dysplasia, nonlethal dominant","type":"related"},{"name":"metatropic dysplasia","type":"exact"}],"termid":"MONDO:0007986","xrefs":{"Monarch":{"xref_id":"0007986"}}}


id: PBO:0087707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; essential for basal and activated transcription; direct target of Cyc8p-Tup1p transcriptional corepressor","termid":"PBO:0087707"}


id: GO:0009738
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated by the binding of the plant hormone abscisic acid (ABA) to a receptor, and ending with modulation of a cellular process, e.g. transcription.","definition_xrefs":["GOC:sm","GOC:signaling","PMID:24269821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone-mediated signaling pathway","termid":"GO:0009755"},{"relation_name":"part_of","term_name":"cellular response to abscisic acid stimulus","termid":"GO:0071215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"abscisic acid-activated signaling pathway","synonyms":[{"name":"ABA signal transduction","type":"exact"},{"name":"ABA signaling","type":"exact"},{"name":"abscisic acid mediated signalling","type":"exact"},{"name":"abscisic acid signal transduction","type":"related"},{"name":"abscisic acid-mediated signaling pathway","type":"related"}],"termid":"GO:0009738"}


id: GO:0005893
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that binds interleukin-2; comprises alpha, beta, and gamma subunits.","definition_xrefs":["PMID:8266078","GOC:mah","PMID:3116143"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane signaling receptor complex","termid":"GO:0098802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"interleukin-2 receptor complex","synonyms":[{"name":"IL-2 receptor complex","type":"exact"}],"termid":"GO:0005893"}


id: FYPO:0004909
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein that is normally localized to discrete regions in the nucleus, visible as foci or dots by microscopy, is abnormally localized such that dots cannot be observed, and the protein is instead distributed throughout the nucleus.","definition_xrefs":["PomBase:mah","PMID:8937982"],"direct_ancestors":[{"relation_name":"is_a","term_name":"loss of punctate nuclear protein localization","termid":"FYPO:0005863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"loss of punctate nuclear protein localization, with protein distributed in nucleus","synonyms":[{"name":"abolished punctate nuclear protein localization, with protein distributed in nucleus","type":"exact"},{"name":"loss of punctate nuclear protein localisation, with protein distributed in nucleus","type":"exact"},{"name":"loss of punctate nuclear protein localization, with protein dispersed through nucleus","type":"exact"},{"name":"loss of punctate nuclear protein localization, with protein distributed in nucleus, during mitotic cell cycle","type":"related"},{"name":"loss of punctate nuclear protein localization, with protein distributed in nucleus, during vegetative growth","type":"exact"},{"name":"loss of punctate nuclear protein localization, with protein distributed throughout nucleus","type":"exact"}],"termid":"FYPO:0004909"}


id: PBO:0002000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartic protease Sxa1","termid":"PBO:0002000"}


id: GO:0005579
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex produced by sequentially activated components of the complement cascade inserted into a target cell membrane and forming a pore leading to cell lysis via ion and water flow.","definition_xrefs":["GOC:add","ISBN:068340007X","ISBN:0781735149","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pore complex","termid":"GO:0046930"},{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"membrane attack complex","secondary_identifiers":["Wikipedia:Complement_membrane_attack_complex"],"synonyms":[{"name":"MAC","type":"exact"},{"name":"TCC","type":"exact"},{"name":"membrane attack complex protein alphaM chain","type":"narrow"},{"name":"membrane attack complex protein beta2 chain","type":"narrow"},{"name":"terminal complement complex","type":"exact"}],"termid":"GO:0005579"}


id: PBO:0004195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INCENP, Pic1","termid":"PBO:0004195"}


id: GO:0033675
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bounded vesicle found near the apical, or pericanalicular, membrane of a hepatocyte; contains proteins involved in bile salt transport and other fluid and solute transport processes.","definition_xrefs":["PMID:9790571","PMID:15763347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle","termid":"GO:0031410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"pericanalicular vesicle","termid":"GO:0033675"}


id: PR:O43057
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A guanine nucleotide exchange factor MSS4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13276:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanine nucleotide exchange factor MSS4 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4C3.04c","secondary_identifiers":["UniProtKB:O43057"],"synonyms":[{"name":"Spom972h-RABIF","type":"exact"}],"termid":"PR:O43057"}


id: MONDO:0016053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Isolated cerebellar vermis hypoplasia is a rare, non-syndromic cerebellar malformation characterized by an underdeveloped cerebellar vermis. Patients may present a variable phenotype ranging from normal neurodevelopment to motor and/or language delay, variable degrees of cognitive impairment, hypotonia, equilibrium disturbances, static/dynamic ataxia, oculomotor abnormalities, epilepsy and/or clumsiness. Behavioral disorders such as attention deficit hyperactivity disorder and generalized anxiety have also been reported. Brain MRI may reveal diffuse or selective (mostly posterior) vermian cerebellar hypoplasia and EEG may show focal paroxysms.","definition_xrefs":["Orphanet:199630"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"isolated cerebellar vermis hypoplasia","secondary_identifiers":["GARD:20337","SCTID:766709000","UMLS:C4707794","MEDGEN:1638500"],"termid":"MONDO:0016053","xrefs":{"Monarch":{"xref_id":"0016053"}}}


id: MONDO:0008456
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinocerebellar ataxia with rigidity and peripheral neuropathy","secondary_identifiers":["MESH:C566669","UMLS:C1866770","MEDGEN:401079","OMIM:183050"],"synonyms":[{"name":"spinocerebellar ataxia with rigidity and peripheral neuropathy","type":"exact"}],"termid":"MONDO:0008456","xrefs":{"Monarch":{"xref_id":"0008456"}}}


id: PATO:0000536
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000536 water sensitivity value (obsolete PATO:0000536)","termid":"PATO:0000536"}


id: MONDO:0007199
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"blepharochalasis, superior","secondary_identifiers":["OMIM:110000","MEDGEN:349465","MESH:C566223","UMLS:C1862275"],"synonyms":[{"name":"blepharochalasis, superior","type":"exact"}],"termid":"MONDO:0007199","xrefs":{"Monarch":{"xref_id":"0007199"}}}


id: MONDO:0043343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Interposition of a portion of the colon (e.g., sigmoid colon) between the liver and the diaphragm. It is associated with abdominal pain, vomiting, constipation, anorexia and volvulus. Chilaiditi anomaly refers to asymptomatic interposition.","definition_xrefs":["MESH:D059269"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colonic disorder","termid":"MONDO:0003409"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"Chilaiditi syndrome","secondary_identifiers":["SCTID:14911005","UMLS:C0267494","MEDGEN:452355"],"synonyms":[{"name":"Chilaiditi anomaly","type":"related"},{"name":"Chilaiditi's anomaly","type":"related"},{"name":"Chilaiditi's syndrome","type":"related"},{"name":"Chilaiditis anomaly","type":"related"},{"name":"Chilaiditis syndrome","type":"related"},{"name":"anomaly, Chilaiditi","type":"related"},{"name":"anomaly, Chilaiditi's","type":"related"},{"name":"chilaiditi's syndrome","type":"related"},{"name":"hepatodiaphragmatic colonic interposition","type":"related"},{"name":"subphrenic interposition syndrome","type":"exact"},{"name":"syndrome, Chilaiditi","type":"related"},{"name":"syndrome, Chilaiditi's","type":"related"}],"termid":"MONDO:0043343","xrefs":{"Monarch":{"xref_id":"0043343"}}}


id: PBO:0068207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 514","termid":"PBO:0068207"}


id: FYPO:0004910
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein that is localized normally (i.e. indistinguishably from wild type) to discrete regions in the nucleus, visible as foci or dots by microscopy.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to nucleus during vegetative growth","termid":"FYPO:0000838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000138","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal punctate nuclear protein localization","synonyms":[{"name":"normal punctate nuclear protein localisation","type":"exact"},{"name":"normal punctate nuclear protein localization during mitotic cell cycle","type":"related"},{"name":"normal punctate nuclear protein localization during vegetative growth","type":"exact"}],"termid":"FYPO:0004910"}


id: MONDO:1010702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pyruvate kinase deficiency of erythrocyte that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate kinase deficiency of erythrocyte, non-human animal","termid":"MONDO:1010099"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate kinase deficiency of erythrocyte, domestic cat","secondary_identifiers":["OMIA:000844-9685"],"termid":"MONDO:1010702","xrefs":{"Monarch":{"xref_id":"1010702"}}}


id: GO:0043819
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + H2O + precorrin-5 = S-adenosyl-L-homocysteine + acetate + 2 H+ + precorrin-6X.","definition_xrefs":["EC:2.1.1.152","RHEA:18261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"precorrin-6A synthase (deacetylating) activity","secondary_identifiers":["MetaCyc:R322-RXN","KEGG_REACTION:R05219"],"synonyms":[{"name":"CobF","type":"related"},{"name":"S-adenosyl-L-methionine:precorrin-5 C1-methyltransferase (deacetylating)","type":"exact"},{"name":"precorrin-6X synthase (deacetylating) activity","type":"related"}],"termid":"GO:0043819"}


id: PBO:0017602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP cyclohydrolase Rib1 (predicted)","termid":"PBO:0017602"}


id: PBO:0066728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 25","termid":"PBO:0066728"}


id: GO:0061610
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways in which glycerol, 1,2,3-propanetriol, is converted to glycerone phosphate.","definition_xrefs":["ISBN:0201090910","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerol metabolic process","termid":"GO:0006071"},{"relation_name":"is_a","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"},{"relation_name":"is_a","term_name":"organophosphate metabolic process","termid":"GO:0019637"},{"relation_name":"is_a","term_name":"primary alcohol metabolic process","termid":"GO:0034308"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"glycerol to glycerone phosphate metabolic process","synonyms":[{"name":"glycerol metabolism to DHAP","type":"exact"},{"name":"glycerol metabolism to dihydroxyacetone phosphate","type":"exact"},{"name":"glycerol metabolism to glycerone phosphate","type":"exact"},{"name":"glycerol to DHAP metabolic process","type":"exact"},{"name":"glycerol to dihydroxyacetone phosphate metabolic process","type":"exact"}],"termid":"GO:0061610"}


id: MONDO:0022913
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cutler bass Romshe syndrome (obsolete MONDO:0022913)","termid":"MONDO:0022913","xrefs":{"Monarch":{"xref_id":"0022913"}}}


id: GO:1901837
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of transcription of nuclear large rRNA transcript mediated by RNA polymerase I.","definition_xrefs":["GOC:TermGenie","GOC:sart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transcription by RNA polymerase I","termid":"GO:0016479"},{"relation_name":"is_a","term_name":"regulation of transcription of nucleolar large rRNA by RNA polymerase I","termid":"GO:1901836"},{"relation_name":"negatively_regulates","term_name":"nucleolar large rRNA transcription by RNA polymerase I","termid":"GO:0042790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"negatively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"}],"interesting_parent_ids":["GO:0006355","GO:0008150","GO:0010467","GO:0006351"],"is_obsolete":false,"name":"negative regulation of transcription of nucleolar large rRNA by RNA polymerase I","synonyms":[{"name":"down regulation of transcription of nuclear large rRNA transcript from RNA polymerase I promoter","type":"exact"},{"name":"down regulation of transcription of nuclear rRNA large Pol I transcript","type":"exact"},{"name":"down-regulation of transcription of nuclear large rRNA transcript from RNA polymerase I promoter","type":"exact"},{"name":"down-regulation of transcription of nuclear rRNA large Pol I transcript","type":"exact"},{"name":"downregulation of transcription of nuclear large rRNA transcript from RNA polymerase I promoter","type":"exact"},{"name":"downregulation of transcription of nuclear rRNA large Pol I transcript","type":"exact"},{"name":"inhibition of transcription of nuclear large rRNA transcript from RNA polymerase I promoter","type":"narrow"},{"name":"inhibition of transcription of nuclear rRNA large Pol I transcript","type":"exact"},{"name":"negative regulation of transcription of nuclear large rRNA transcript from RNA polymerase I promoter","type":"exact"},{"name":"negative regulation of transcription of nuclear rRNA large Pol I transcript","type":"exact"}],"termid":"GO:1901837"}


id: MONDO:0001790
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign adipose tissue neoplasm of the spinal cord. It is usually associated with dysraphism in which the intraspinal component communicates with a subcutaneous lipoma through a defect in the posterior elements of the spine. Non-dysraphic intramedullary spinal cord lipomas are very rare.","definition_xrefs":["NCIT:C4619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system lipoma","termid":"MONDO:0003844"},{"relation_name":"is_a","term_name":"benign neoplasm of spinal cord","termid":"MONDO:0021506"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal cord lipoma","secondary_identifiers":["Orphanet:645276","ICD9:214.8","DOID:13743","SCTID:189017000","UMLS:C0347446","NANDO:2200815","MEDGEN:91131"],"synonyms":[{"name":"lipoma of spinal cord","type":"exact"},{"name":"spinal cord lipoma","type":"exact"}],"termid":"MONDO:0001790","xrefs":{"Monarch":{"xref_id":"0001790"}}}


id: GO:0016043
data:
  {"annotated_genes":["SJAG_00771","SJAG_04397","SJAG_01204","SJAG_00053","SJAG_05302","SJAG_04891","SJAG_04595","SJAG_02248","SJAG_04197","SJAG_02186","SJAG_04690","SJAG_02065","SJAG_03229","SJAG_03472","SJAG_03625","SJAG_01229","SJAG_00364","SJAG_03146","SJAG_04748","SJAG_02748","SJAG_02335","SJAG_04259","SJAG_02228","SJAG_01448","SJAG_00972","SJAG_02592","SJAG_02624","SJAG_01459","SJAG_03026","SJAG_04624","SJAG_02609","SJAG_02319","SJAG_03683","SJAG_03721","SJAG_02265","SJAG_00146","SJAG_04012","SJAG_00722","SJAG_03217","SJAG_02348","SJAG_03460","SJAG_04884","SJAG_04255","SJAG_00794","SJAG_04455","SJAG_05221","SJAG_02915","SJAG_03070","SJAG_04996","SJAG_02563","SJAG_04492","SJAG_03327","SJAG_04561","SJAG_06514","SJAG_04724","SJAG_00618","SJAG_01948","SJAG_00145","SJAG_03983","SJAG_00766","SJAG_02164","SJAG_00701","SJAG_04073","SJAG_02723","SJAG_01571","SJAG_00320","SJAG_04237","SJAG_01832","SJAG_03440","SJAG_02566","SJAG_02581","SJAG_00323","SJAG_01816","SJAG_00642","SJAG_03095","SJAG_04943","SJAG_00078","SJAG_03033","SJAG_00896","SJAG_03153","SJAG_03255","SJAG_02215","SJAG_02798","SJAG_02571","SJAG_01836","SJAG_01823","SJAG_03862","SJAG_03630","SJAG_00634","SJAG_04930","SJAG_02456","SJAG_02640","SJAG_00441","SJAG_01777","SJAG_01945","SJAG_01171","SJAG_03155","SJAG_04150","SJAG_04639","SJAG_00029","SJAG_00279","SJAG_03200","SJAG_01748","SJAG_00335","SJAG_03892","SJAG_03957","SJAG_05313","SJAG_03072","SJAG_01207","SJAG_00735","SJAG_04791","SJAG_02479","SJAG_04855","SJAG_04911","SJAG_02607","SJAG_01228","SJAG_05679","SJAG_04332","SJAG_03399","SJAG_05017","SJAG_02535","SJAG_00229","SJAG_03688","SJAG_01339","SJAG_02362","SJAG_01180","SJAG_03792","SJAG_04602","SJAG_01252","SJAG_02208","SJAG_03846","SJAG_03628","SJAG_03995","SJAG_05193","SJAG_02659","SJAG_01831","SJAG_05261","SJAG_04528","SJAG_02683","SJAG_04746","SJAG_02528","SJAG_02350","SJAG_00970","SJAG_04413","SJAG_04014","SJAG_03748","SJAG_01373","SJAG_03710","SJAG_01008","SJAG_00079","SJAG_03907","SJAG_04671","SJAG_02990","SJAG_04183","SJAG_01165","SJAG_05280","SJAG_02034","SJAG_01999","SJAG_03720","SJAG_02831","SJAG_03848","SJAG_02638","SJAG_02339","SJAG_03116","SJAG_01864","SJAG_00908","SJAG_02649","SJAG_00268","SJAG_04947","SJAG_01331","SJAG_03725","SJAG_03287","SJAG_00961","SJAG_04898","SJAG_00424","SJAG_04950","SJAG_05207","SJAG_01233","SJAG_00523","SJAG_02759","SJAG_02869","SJAG_03812","SJAG_01324","SJAG_05223","SJAG_02733","SJAG_00301","SJAG_03551","SJAG_03906","SJAG_02384","SJAG_01152","SJAG_04180","SJAG_00810","SJAG_00557","SJAG_03013","SJAG_03558","SJAG_03839","SJAG_03773","SJAG_01675","SJAG_00526","SJAG_04644","SJAG_01388","SJAG_01696","SJAG_05950","SJAG_03106","SJAG_01804","SJAG_01483","SJAG_04203","SJAG_03219","SJAG_00496","SJAG_01708","SJAG_00700","SJAG_02619","SJAG_01928","SJAG_00087","SJAG_00821","SJAG_02830","SJAG_04317","SJAG_05192","SJAG_00934","SJAG_02558","SJAG_00277","SJAG_04271","SJAG_06309","SJAG_01992","SJAG_04461","SJAG_00322","SJAG_04256","SJAG_04844","SJAG_01622","SJAG_03299","SJAG_02469","SJAG_02427","SJAG_00353","SJAG_03046","SJAG_03366","SJAG_00783","SJAG_05241","SJAG_04670","SJAG_00943","SJAG_04003","SJAG_04077","SJAG_00350","SJAG_01615","SJAG_01268","SJAG_03915","SJAG_03705","SJAG_04793","SJAG_03592","SJAG_03864","SJAG_00984","SJAG_01785","SJAG_03042","SJAG_01711","SJAG_01003","SJAG_00369","SJAG_01658","SJAG_03044","SJAG_00949","SJAG_00845","SJAG_02311","SJAG_02202","SJAG_01644","SJAG_04040","SJAG_02514","SJAG_04816","SJAG_00572","SJAG_04758","SJAG_02166","SJAG_02441","SJAG_01116","SJAG_02595","SJAG_02457","SJAG_01356","SJAG_04776","SJAG_03120","SJAG_00266","SJAG_02560","SJAG_03062","SJAG_02458","SJAG_02864","SJAG_02848","SJAG_00030","SJAG_01760","SJAG_03783","SJAG_03123","SJAG_03689","SJAG_04781","SJAG_02336","SJAG_01732","SJAG_00894","SJAG_02980","SJAG_04008","SJAG_02726","SJAG_00687","SJAG_02477","SJAG_02075","SJAG_04196","SJAG_07002","SJAG_03795","SJAG_00380","SJAG_05373","SJAG_00840","SJAG_03209","SJAG_01716","SJAG_03137","SJAG_02465","SJAG_03718","SJAG_00259","SJAG_03189","SJAG_03038","SJAG_02040","SJAG_00113","SJAG_04470","SJAG_00045","SJAG_05323","SJAG_03437","SJAG_00474","SJAG_02414","SJAG_02439","SJAG_02886","SJAG_04280","SJAG_00898","SJAG_00153","SJAG_04524","SJAG_04372","SJAG_00907","SJAG_00600","SJAG_04097","SJAG_00942","SJAG_04272","SJAG_00638","SJAG_00684","SJAG_02746","SJAG_06468","SJAG_04190","SJAG_02989","SJAG_00855","SJAG_02570","SJAG_04862","SJAG_00718","SJAG_04978","SJAG_05260","SJAG_03905","SJAG_00327","SJAG_02245","SJAG_00514","SJAG_04253","SJAG_03703","SJAG_01282","SJAG_02788","SJAG_01665","SJAG_01940","SJAG_03145","SJAG_01419","SJAG_03313","SJAG_04208","SJAG_04965","SJAG_00870","SJAG_03428","SJAG_00974","SJAG_00231","SJAG_00147","SJAG_03048","SJAG_02323","SJAG_03221","SJAG_03011","SJAG_01870","SJAG_04412","SJAG_02329","SJAG_04643","SJAG_01731","SJAG_02035","SJAG_00307","SJAG_00596","SJAG_04734","SJAG_03493","SJAG_01564","SJAG_03357","SJAG_00752","SJAG_01722","SJAG_03751","SJAG_04661","SJAG_01951","SJAG_01465","SJAG_03525","SJAG_00900","SJAG_01377","SJAG_00313","SJAG_04615","SJAG_01200","SJAG_04140","SJAG_03746","SJAG_01837","SJAG_02401","SJAG_02480","SJAG_02656","SJAG_00286","SJAG_05231","SJAG_01327","SJAG_02204","SJAG_04498","SJAG_07018","SJAG_04227","SJAG_03603","SJAG_00302","SJAG_03782","SJAG_03455","SJAG_04186","SJAG_05019","SJAG_02704","SJAG_01046","SJAG_04573","SJAG_00868","SJAG_03045","SJAG_04417","SJAG_01756","SJAG_02667","SJAG_04076","SJAG_01888","SJAG_01385","SJAG_02185","SJAG_04205","SJAG_03041","SJAG_04703","SJAG_03680","SJAG_00603","SJAG_00697","SJAG_02169","SJAG_02498","SJAG_03322","SJAG_01697","SJAG_03873","SJAG_02315","SJAG_04684","SJAG_01662","SJAG_03646","SJAG_02177","SJAG_01193","SJAG_05245","SJAG_05185","SJAG_01780","SJAG_01127","SJAG_01677","SJAG_04464","SJAG_03080","SJAG_03012","SJAG_01943","SJAG_03941","SJAG_03548","SJAG_02361","SJAG_03170","SJAG_00584","SJAG_01599","SJAG_04922","SJAG_02541","SJAG_03128","SJAG_04598","SJAG_05345","SJAG_05333","SJAG_01594","SJAG_01072","SJAG_04999","SJAG_02170","SJAG_03347","SJAG_03023","SJAG_00411","SJAG_04049","SJAG_01460","SJAG_00756","SJAG_03172","SJAG_03047","SJAG_02761","SJAG_02695","SJAG_01878","SJAG_00666","SJAG_03780","SJAG_00429","SJAG_03431","SJAG_00768","SJAG_04879","SJAG_01379","SJAG_03724","SJAG_03784","SJAG_02846","SJAG_00532","SJAG_03774","SJAG_00416","SJAG_03286","SJAG_00368","SJAG_01540","SJAG_01567","SJAG_04509","SJAG_01956","SJAG_02778","SJAG_01707","SJAG_01076","SJAG_02294","SJAG_03424","SJAG_00678","SJAG_04886","SJAG_03619","SJAG_02303","SJAG_05282","SJAG_07008","SJAG_05372","SJAG_02866","SJAG_04883","SJAG_03301","SJAG_01964","SJAG_03631","SJAG_01225","SJAG_04960","SJAG_04822","SJAG_00581","SJAG_00852","SJAG_01839","SJAG_05161","SJAG_04972","SJAG_04909","SJAG_00746","SJAG_06392","SJAG_03279","SJAG_04668","SJAG_03844","SJAG_04992","SJAG_01325","SJAG_02812","SJAG_04052","SJAG_00587","SJAG_02513","SJAG_01224","SJAG_04522","SJAG_04343","SJAG_04508","SJAG_02589","SJAG_02381","SJAG_16457","SJAG_01771","SJAG_01653","SJAG_04699","SJAG_02621","SJAG_00442","SJAG_01769","SJAG_04982","SJAG_03787","SJAG_02736","SJAG_04274","SJAG_00172","SJAG_00589","SJAG_03496","SJAG_01111","SJAG_01227","SJAG_03579","SJAG_03282","SJAG_04338","SJAG_01141","SJAG_04468","SJAG_00545","SJAG_00140","SJAG_02267","SJAG_01838","SJAG_00330","SJAG_04596","SJAG_03345","SJAG_05295","SJAG_01386","SJAG_03884","SJAG_03655","SJAG_04108","SJAG_01516","SJAG_01805","SJAG_00954","SJAG_00466","SJAG_00142","SJAG_00225","SJAG_01834","SJAG_00757","SJAG_03694","SJAG_04257","SJAG_03681","SJAG_01453","SJAG_01422","SJAG_01685","SJAG_04623","SJAG_00018","SJAG_03268","SJAG_02594","SJAG_05353","SJAG_00004","SJAG_06597","SJAG_01251","SJAG_02376","SJAG_03220","SJAG_04857","SJAG_03930","SJAG_05240","SJAG_06608","SJAG_01270","SJAG_02332","SJAG_02539","SJAG_00261","SJAG_04315","SJAG_03537","SJAG_00669","SJAG_04669","SJAG_02838","SJAG_04303","SJAG_06270","SJAG_04513","SJAG_04294","SJAG_05179","SJAG_03052","SJAG_03894","SJAG_02342","SJAG_00114","SJAG_02375","SJAG_05266","SJAG_01420","SJAG_03486","SJAG_00303","SJAG_01640","SJAG_03835","SJAG_00349","SJAG_03898","SJAG_02701","SJAG_04347","SJAG_01009","SJAG_01772","SJAG_01456","SJAG_01648","SJAG_04146","SJAG_03954","SJAG_02373","SJAG_01611","SJAG_02314","SJAG_05105","SJAG_05226","SJAG_03119","SJAG_00676","SJAG_00913","SJAG_03247","SJAG_03296","SJAG_01161","SJAG_02549","SJAG_03552","SJAG_02226","SJAG_02295","SJAG_02380","SJAG_01274","SJAG_03007","SJAG_01633","SJAG_03353","SJAG_03938","SJAG_01774","SJAG_00154","SJAG_04620","SJAG_02119","SJAG_03222","SJAG_00188","SJAG_00126","SJAG_01378","SJAG_02601","SJAG_01863","SJAG_04213","SJAG_03073","SJAG_01929","SJAG_03936","SJAG_01230","SJAG_02511","SJAG_04696","SJAG_00152","SJAG_00230","SJAG_02516","SJAG_01305","SJAG_03315","SJAG_01454","SJAG_02509","SJAG_02561","SJAG_04214","SJAG_03386","SJAG_01497","SJAG_02116","SJAG_00646","SJAG_01759","SJAG_02246","SJAG_02771","SJAG_01939","SJAG_06135","SJAG_02079","SJAG_01156","SJAG_03536","SJAG_00610","SJAG_00906","SJAG_01140","SJAG_00168","SJAG_07005","SJAG_00703","SJAG_01301","SJAG_00072","SJAG_00204","SJAG_01371","SJAG_00455","SJAG_04177","SJAG_00440","SJAG_02957","SJAG_03563","SJAG_01996","SJAG_00476","SJAG_00682","SJAG_01530","SJAG_00882","SJAG_04379","SJAG_00689","SJAG_00338","SJAG_01782","SJAG_00186","SJAG_02814","SJAG_04599","SJAG_04942","SJAG_03591","SJAG_00402","SJAG_03685","SJAG_01068","SJAG_04553","SJAG_02981","SJAG_02198","SJAG_02725","SJAG_01925","SJAG_00645","SJAG_05297","SJAG_00206","SJAG_00769","SJAG_03599","SJAG_01181","SJAG_04418","SJAG_04900","SJAG_03682","SJAG_03147","SJAG_02908","SJAG_02613","SJAG_03540","SJAG_04479","SJAG_05248","SJAG_01417","SJAG_05220","SJAG_00680","SJAG_03324","SJAG_04038","SJAG_01912","SJAG_04768","SJAG_03624","SJAG_02165","SJAG_04621","SJAG_03575","SJAG_00414","SJAG_01317","SJAG_02943","SJAG_00486","SJAG_03342","SJAG_03435","SJAG_04989","SJAG_01050","SJAG_04534","SJAG_00293","SJAG_03832","SJAG_00661","SJAG_01410","SJAG_04093","SJAG_02718","SJAG_02995","SJAG_01329","SJAG_01610","SJAG_03393","SJAG_03379","SJAG_00170","SJAG_02698","SJAG_04370","SJAG_02104","SJAG_04578","SJAG_05978","SJAG_01464","SJAG_03891","SJAG_03543","SJAG_02895","SJAG_05329","SJAG_00823","SJAG_01833","SJAG_01579","SJAG_02822","SJAG_02845","SJAG_02556","SJAG_03673","SJAG_00649","SJAG_04322","SJAG_02870","SJAG_05300","SJAG_00739","SJAG_03776","SJAG_02757","SJAG_00640","SJAG_03463","SJAG_02500","SJAG_03542","SJAG_04918","SJAG_01606","SJAG_02664","SJAG_00973","SJAG_00521","SJAG_01016","SJAG_01825","SJAG_01297","SJAG_05001","SJAG_04163","SJAG_01561","SJAG_02817","SJAG_03798","SJAG_02433","SJAG_01299","SJAG_00171","SJAG_03596","SJAG_00559","SJAG_00460","SJAG_03609","SJAG_04991","SJAG_03916","SJAG_05195","SJAG_00333","SJAG_01296","SJAG_04887","SJAG_03956","SJAG_04936","SJAG_01568","SJAG_06641","SJAG_04004","SJAG_02349","SJAG_03092","SJAG_02114","SJAG_04654","SJAG_01745","SJAG_04502","SJAG_06642","SJAG_04126","SJAG_05032","SJAG_03323","SJAG_02392","SJAG_01048","SJAG_04547","SJAG_01713","SJAG_00160","SJAG_04059","SJAG_01283","SJAG_01807","SJAG_03855","SJAG_01290","SJAG_02731","SJAG_03544","SJAG_04148","SJAG_00891","SJAG_02254","SJAG_01005","SJAG_04005","SJAG_02351","SJAG_04940","SJAG_04030","SJAG_00357","SJAG_04016","SJAG_02652","SJAG_02390","SJAG_04554","SJAG_02002","SJAG_01504","SJAG_00185","SJAG_01601","SJAG_03183","SJAG_04462","SJAG_05237","SJAG_04655","SJAG_03602","SJAG_03567","SJAG_01073","SJAG_05199","SJAG_02952","SJAG_02532","SJAG_03161","SJAG_05315","SJAG_01063","SJAG_04763","SJAG_01188","SJAG_00118","SJAG_00723","SJAG_03006","SJAG_03997","SJAG_03099","SJAG_03491","SJAG_02693","SJAG_03502","SJAG_03945","SJAG_04981","SJAG_00980","SJAG_02873","SJAG_03338","SJAG_04666","SJAG_16459","SJAG_00856","SJAG_05180","SJAG_05979","SJAG_04001","SJAG_01437","SJAG_00623","SJAG_02843","SJAG_01223","SJAG_01819","SJAG_02451","SJAG_02304","SJAG_01513","SJAG_02074","SJAG_04428","SJAG_00859","SJAG_02840","SJAG_01775","SJAG_02924","SJAG_02524","SJAG_03285","SJAG_05000","SJAG_01374","SJAG_04469","SJAG_04732","SJAG_03900","SJAG_00336","SJAG_01826","SJAG_02997","SJAG_00925","SJAG_01214","SJAG_03593","SJAG_01169","SJAG_04995","SJAG_03182","SJAG_04389","SJAG_02576","SJAG_04266","SJAG_03395","SJAG_03574","SJAG_02658","SJAG_00899","SJAG_00058","SJAG_00569","SJAG_02813","SJAG_01545","SJAG_03464","SJAG_04369","SJAG_02229","SJAG_05003","SJAG_01017","SJAG_06440","SJAG_02663","SJAG_01217","SJAG_00641","SJAG_04116","SJAG_03441","SJAG_00163","SJAG_02684","SJAG_05344","SJAG_00198","SJAG_04538","SJAG_03581","SJAG_02447","SJAG_02508","SJAG_02645","SJAG_03701","SJAG_01867","SJAG_04304","SJAG_03068","SJAG_02455","SJAG_01240","SJAG_03722","SJAG_00938","SJAG_00184","SJAG_03949","SJAG_04287","SJAG_01215","SJAG_00298","SJAG_02490","SJAG_02270","SJAG_03416","SJAG_02366","SJAG_02045","SJAG_01330","SJAG_01120","SJAG_01835","SJAG_01546","SJAG_00418","SJAG_00983","SJAG_05321","SJAG_00207","SJAG_04283","SJAG_01263","SJAG_00959","SJAG_03982","SJAG_00244","SJAG_02712","SJAG_03867","SJAG_02803","SJAG_01794","SJAG_02868","SJAG_03627","SJAG_00228","SJAG_04387","SJAG_04574","SJAG_01407","SJAG_01938","SJAG_01475","SJAG_03700","SJAG_00911","SJAG_04529","SJAG_02872","SJAG_00513","SJAG_05309","SJAG_01095","SJAG_01320","SJAG_03418","SJAG_04853","SJAG_03515","SJAG_03458","SJAG_02346","SJAG_05184","SJAG_05290","SJAG_04745","SJAG_03090","SJAG_00216","SJAG_03036","SJAG_03438","SJAG_04039","SJAG_03465","SJAG_04114","SJAG_02028","SJAG_04143","SJAG_00611","SJAG_02306","SJAG_00354","SJAG_04755","SJAG_01741","SJAG_03487","SJAG_00871","SJAG_03469","SJAG_04290","SJAG_00692","SJAG_02707","SJAG_01547","SJAG_02087","SJAG_04613","SJAG_05020","SJAG_03781","SJAG_01146","SJAG_05194","SJAG_02437","SJAG_00743","SJAG_05289","SJAG_04293","SJAG_03387","SJAG_03635","SJAG_03698","SJAG_00341","SJAG_03264","SJAG_01652","SJAG_03944","SJAG_05273","SJAG_00510","SJAG_03403","SJAG_00741","SJAG_02763","SJAG_01926","SJAG_03704","SJAG_04358","SJAG_00939","SJAG_02700","SJAG_04044","SJAG_01242","SJAG_03752","SJAG_04530","SJAG_03050","SJAG_03295","SJAG_04531","SJAG_02194","SJAG_00719","SJAG_02189","SJAG_02241","SJAG_03887","SJAG_04232","SJAG_04966","SJAG_04739","SJAG_04064","SJAG_03118","SJAG_05285","SJAG_04560","SJAG_05196","SJAG_02394","SJAG_00643","SJAG_02626","SJAG_03270","SJAG_05306","SJAG_05414","SJAG_01679","SJAG_01315","SJAG_00667","SJAG_00578","SJAG_01590","SJAG_03851","SJAG_01044","SJAG_02708","SJAG_02573","SJAG_04566","SJAG_04998","SJAG_01526","SJAG_02019","SJAG_02756","SJAG_01680","SJAG_02691","SJAG_00404","SJAG_04815","SJAG_01321","SJAG_02263","SJAG_04899","SJAG_01467","SJAG_00806","SJAG_01440","SJAG_02379","SJAG_01067","SJAG_04692","SJAG_04074","SJAG_01168","SJAG_00064","SJAG_06046","SJAG_02382","SJAG_00930","SJAG_00935","SJAG_00551","SJAG_04375","SJAG_02629","SJAG_01761","SJAG_02975","SJAG_03926","SJAG_00918","SJAG_02446","SJAG_03664","SJAG_01548","SJAG_01357","SJAG_05209","SJAG_04080","SJAG_00397","SJAG_00449","SJAG_01523","SJAG_00796","SJAG_02768","SJAG_01138","SJAG_03394","SJAG_05173","SJAG_01654","SJAG_04312","SJAG_02587","SJAG_00247","SJAG_04319","SJAG_00355","SJAG_01143","SJAG_04454","SJAG_02066","SJAG_02979","SJAG_03193","SJAG_02187","SJAG_05398","SJAG_00218","SJAG_03741","SJAG_01538","SJAG_01075","SJAG_00873","SJAG_02330","SJAG_00430","SJAG_04023","SJAG_04586","SJAG_01613","SJAG_03250","SJAG_02606","SJAG_03356","SJAG_03508","SJAG_03025","SJAG_00597","SJAG_04230","SJAG_03576","SJAG_00498","SJAG_02064","SJAG_03125","SJAG_01262","SJAG_02699","SJAG_01895","SJAG_00100","SJAG_03670","SJAG_03380","SJAG_01518","SJAG_04968","SJAG_03843","SJAG_02385","SJAG_04457","SJAG_03453","SJAG_01598","SJAG_01790","SJAG_04483","SJAG_01537","SJAG_02916","SJAG_00377","SJAG_01470","SJAG_03005","SJAG_03658","SJAG_00066","SJAG_02192","SJAG_02416","SJAG_02340","SJAG_00912","SJAG_03361","SJAG_04396","SJAG_04141","SJAG_00405","SJAG_02497","SJAG_00284","SJAG_00304","SJAG_02590","SJAG_02616","SJAG_01384","SJAG_01278","SJAG_03942","SJAG_00858","SJAG_04010","SJAG_03337","SJAG_02120","SJAG_03989","SJAG_01178","SJAG_01917","SJAG_02409","SJAG_01074","SJAG_01949","SJAG_02807","SJAG_01238","SJAG_00971","SJAG_03162","SJAG_01873","SJAG_03986","SJAG_04275","SJAG_02338","SJAG_02174","SJAG_02529","SJAG_02222","SJAG_01211","SJAG_03444","SJAG_02737","SJAG_02906","SJAG_04245","SJAG_03758","SJAG_02096","SJAG_03617","SJAG_04744","SJAG_04901","SJAG_02436","SJAG_00662","SJAG_01122","SJAG_03449","SJAG_02279","SJAG_03168","SJAG_05009","SJAG_02878","SJAG_00217","SJAG_03889","SJAG_02651","SJAG_03126","SJAG_02081","SJAG_01515","SJAG_02320","SJAG_02501","SJAG_04061","SJAG_00187","SJAG_01082","SJAG_02466","SJAG_02210","SJAG_01811","SJAG_03086","SJAG_02213","SJAG_03421","SJAG_04576","SJAG_03230","SJAG_00082","SJAG_02398","SJAG_01876","SJAG_00727","SJAG_00031","SJAG_05305","SJAG_04638","SJAG_01511","SJAG_02672","SJAG_03637","SJAG_02754","SJAG_05025","SJAG_02994","SJAG_04355","SJAG_03987","SJAG_05265","SJAG_01894","SJAG_02622","SJAG_00594","SJAG_00326","SJAG_00914","SJAG_04391","SJAG_04863","SJAG_04640","SJAG_02100","SJAG_03668","SJAG_02132","SJAG_04489","SJAG_02797","SJAG_04348","SJAG_03214","SJAG_02184","SJAG_00677","SJAG_04752","SJAG_03157","SJAG_03633","SJAG_02542","SJAG_04868","SJAG_01212","SJAG_01906","SJAG_02355","SJAG_02212","SJAG_00249","SJAG_04395","SJAG_01848","SJAG_02749","SJAG_04581","SJAG_02460","SJAG_03466","SJAG_01114","SJAG_06002","SJAG_00826","SJAG_02628","SJAG_01487","SJAG_00773","SJAG_03100","SJAG_04558","SJAG_04465","SJAG_01015","SJAG_00702","SJAG_00433","SJAG_01821","SJAG_03865","SJAG_04497","SJAG_01110","SJAG_02181","SJAG_02058","SJAG_02914","SJAG_03401","SJAG_00505","SJAG_04221","SJAG_01993","SJAG_00663","SJAG_02773","SJAG_04100","SJAG_03940","SJAG_01605","SJAG_01808","SJAG_01405","SJAG_04841","SJAG_04450","SJAG_03456","SJAG_04597","SJAG_00436","SJAG_00278","SJAG_02927","SJAG_02551","SJAG_04194","SJAG_01896","SJAG_01370","SJAG_02431","SJAG_03232","SJAG_00564","SJAG_02795","SJAG_04172","SJAG_02286","SJAG_03088","SJAG_03546","SJAG_01503","SJAG_05296","SJAG_07011","SJAG_00308","SJAG_02347","SJAG_02897","SJAG_04603","SJAG_04066","SJAG_05319","SJAG_00883","SJAG_00576","SJAG_05268"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93302,101928,68046,99567,93533,98587,103424,109991,114177,78516,110185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044571"},{"annotations":[88561,110172,109562,118153,101929,99260,93120],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044572"},{"annotations":[75592,77640,103627,91012,73652,73858,95133,79738,100187,105484,112472,103571,88490,110997,103380,112495,98243,100007],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000147"},{"annotations":[98049,105467,99222,95621,88596,99161],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0044396"},{"annotations":[89666],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0051764"},{"annotations":[102437,102829,118795,106730,97529,77545,107360,109055,115184,99860,117434,93997,61630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030036"},{"annotations":[98244,88491,100008,91013,103628,105486,99162,100188],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0090135"},{"annotations":[94163,77580,75291,71891,75942,76402,76705],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0051017"},{"annotations":[99973],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0061572"},{"annotations":[116477],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0061573"},{"annotations":[70324,73774],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0030042"},{"annotations":[71892],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0051639"},{"annotations":[105889],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007015"},{"annotations":[65083,94164,98050,99163],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030041"},{"annotations":[89708],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0045010"},{"annotations":[94914,90204,96180],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051519"},{"annotations":[108281],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0010846"},{"annotations":[111111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000915"},{"annotations":[108446,98613,98355,89668],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0071520"},{"annotations":[105470],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044837"},{"annotations":[80226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031032"},{"annotations":[68941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140331"},{"annotations":[78177,79394,80320,103055,80066,76783,78510,75115,98245,107476],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0034314"},{"annotations":[92109,88552,90587,89044],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030476"},{"annotations":[105297,73431,91840],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031321"},{"annotations":[95706,100227,102028,91630,110424,114234,105611,97917,99154,97880,107697,119314,118832,119132],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032120"},{"annotations":[104445,97881,100160,108030,100159,114235,103234,97201,92631,107150],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031322"},{"annotations":[98303,102837,106324,116077,113205,119197,93148,107749,92727,112448,103823,101056,100916,99503,111121,111750,79635,116076,100724,116948,89965,93554,109321],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1902626"},{"annotations":[109915],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990734"},{"annotations":[76687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060172"},{"annotations":[117238],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0030954"},{"annotations":[106764,100700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030953"},{"annotations":[88209,94170],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051456"},{"annotations":[90381,118443,88344,76158,105798,88096,110625,100701,116823,118957,73187,95892,72433,91723,110670,111992,98232,91332],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051315"},{"annotations":[72978,80675,72655,80006,60276,78674,72520,71100,70906,77137,80094,80038,103903,72508,94962,104924,71786,77318,73833,79090,93251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000045"},{"annotations":[75851,70908,72658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097352"},{"annotations":[94963],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016240"},{"annotations":[92665,76057,80555,79524],"is_not":false,"rel_names":["negatively_regulates","is_a","regulates"],"summary":null,"term":"GO:0051016"},{"annotations":[76653,68283,98272,80059,104368,73154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000492"},{"annotations":[77011,80576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000493"},{"annotations":[114713],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140708"},{"annotations":[100065,107171,116778,88396,111071,118202,103805],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051523"},{"annotations":[73818,96014,114227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006884"},{"annotations":[71732,80234,99463,89213,90403,114524,117994,95033,70589,93134,99715,106682,113418,115382,102385,107658,103222,116766,95804,119113],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0034080"},{"annotations":[102721,109972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140898"},{"annotations":[67483,76449,76886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051131"},{"annotations":[108050,88152,91261,110861,90013,96573,108132,117160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140588"},{"annotations":[57833,77904,113112,67325,113690,64524,106512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006325"},{"annotations":[98472,104948,58563,73155,60291,118017,68722,70547,65049,95653,65864,65186,110509,113386,113827,104749,61205,59348,106832,89166,68630,63998,67549,98798,108235,76654,59226,71361,94293,76829,58562,67876,58192,62083,65638,67437,58848,70770,63211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006338"},{"annotations":[118128],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000354"},{"annotations":[61647,78104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048268"},{"annotations":[80085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072318"},{"annotations":[115706,107660,110250,113870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140529"},{"annotations":[113908],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140719"},{"annotations":[71642,118041],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0048205"},{"annotations":[73402],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090114"},{"annotations":[78782,75394,75163,76847,76023,77436,71720],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090110"},{"annotations":[118203,100497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030866"},{"annotations":[107816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043622"},{"annotations":[78871,107632,75436,79238,89835,102021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042407"},{"annotations":[117254,88404,105894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017004"},{"annotations":[71502,68417,102639,102762,107737,112436,80250,117485,118958,99544,72086,100406,88097,97306],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031122"},{"annotations":[107489,95141,96813,74171,109474,109475,116328,117795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002184"},{"annotations":[104448,97397,111045,105539,95172,99787,87990,104597,92435,98304,116871,116872,111046,102838,104369,105123],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0180023"},{"annotations":[96200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042256"},{"annotations":[91062,108567,107546,114085,114572,99914,112267,116200,104210],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[90070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000917"},{"annotations":[76198,75464,65784,72616,65204],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000730"},{"annotations":[94943,104353,99288,89214,99229,118862,94643,113452,95404,100000,108041,105039,109377,90390,92713,91033,95161,93135,99464,99716,97552,107194,74175,104537,115019,115898],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140861"},{"annotations":[110252,74867,108042,115707,60865,90405,95162,101880,110529,111578,80235,101821,113909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006335"},{"annotations":[113482,59252,70804,72998,119236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006265"},{"annotations":[107974,99381,117095,88881,89502],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990918"},{"annotations":[111710,117240,97905,88098,114250,111362,91724,101050,103281,103573,91333,95542,92182],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030989"},{"annotations":[104191,70151,118143,71725],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070941"},{"annotations":[78770],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0016320"},{"annotations":[72234,90748,94014,119437,73911,74632],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0090158"},{"annotations":[101885,75161],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007029"},{"annotations":[64751],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0071788"},{"annotations":[108876,103773,115270,118886,108956],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990809"},{"annotations":[62331,60565,90749,97787,91822,72235,61472,111972,118459],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061817"},{"annotations":[99837,74930,79963,100039,71594,77472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034058"},{"annotations":[76806,80163,80537,102979,75446],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007032"},{"annotations":[116509,93734,119142,65601,59893,68598,91577],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0040029"},{"annotations":[102640],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031025"},{"annotations":[75235],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034087"},{"annotations":[105189,117241,104860,97308,76698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000132"},{"annotations":[72380],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034085"},{"annotations":[99650,89776,111072,88807,105677,96181,100498,73608],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030950"},{"annotations":[101593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030952"},{"annotations":[77370,79821,99545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030951"},{"annotations":[101423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905143"},{"annotations":[111648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070196"},{"annotations":[62084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903259"},{"annotations":[103539,94416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140718"},{"annotations":[59617,69793,72260,68779,63951,75455,97184,62455,64138,99255,59184,59883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001732"},{"annotations":[71772,78308,78731,73871,96417,118358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001731"},{"annotations":[116479,108448],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0070649"},{"annotations":[105472],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0110009"},{"annotations":[102263,100472,102264,89435,88618,111625,94361,108381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904541"},{"annotations":[110360,71313,79868,102771,74862,78254,71615,75632,80700,71260,77165,75548,76216,78175,76788,89675],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031505"},{"annotations":[78275,106100,58093],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000349"},{"annotations":[105171,73487,77684,109858],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000350"},{"annotations":[77351,94760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034203"},{"annotations":[78564,76805,77274,77969,102500,72679,79073,74813,75680,109807,119103,74389,72521],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007030"},{"annotations":[77970],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048194"},{"annotations":[96279],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048210"},{"annotations":[88497,91093,99230,99446,112920,103371,112921,115555,94417,96492,99472,118052,103540,113358,117421,112919],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0033696"},{"annotations":[70732,74081,73531,92948,94944,115310,115709,75166,114423,77037,94687,119565,119566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031507"},{"annotations":[91682,96981,117449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070828"},{"annotations":[90625,117358,115838,108133,114086,88153,98946,94134,101655],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031619"},{"annotations":[79261,108134,88099,111534,110862],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007129"},{"annotations":[117163,92130,118007,89701],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045143"},{"annotations":[111535,101753,106907],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032118"},{"annotations":[95643],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140456"},{"annotations":[78190,95644,76116],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000073"},{"annotations":[92825,75725],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007007"},{"annotations":[111636,94583,102928,109674,116519,108517,57480],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120009"},{"annotations":[97821,104360,91241,97882,101603,98956,106170,107834,108965,107057,116542,89569,109836,100849,107960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120010"},{"annotations":[106648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120011"},{"annotations":[102641,113072],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0031024"},{"annotations":[92744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009992"},{"annotations":[57359,59038,68826,89614,79403],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016226"},{"annotations":[111773,91725,117242,91334,78992,88100,99546],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000742"},{"annotations":[57113,64612,66939,80171,105799,66336,91118],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0051382"},{"annotations":[76159,91289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051383"},{"annotations":[108568],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099607"},{"annotations":[100413,104848],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903359"},{"annotations":[89933,117359],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030999"},{"annotations":[111299,114489,119177,89109,112369,62417,94986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140042"},{"annotations":[92098,106392,116736,100905,108062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043570"},{"annotations":[104693,90750],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051685"},{"annotations":[70489,96343,99607,101493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043007"},{"annotations":[88599,92854,99305,114624,98615,99224],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1904600"},{"annotations":[103636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140530"},{"annotations":[108031,117540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007127"},{"annotations":[106636,114799],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905318"},{"annotations":[105446,107151,108032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007135"},{"annotations":[90103,64705],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070197"},{"annotations":[87742,90104,100247,103134,105426],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032121"},{"annotations":[116224,100703,109454,102752,95646,99547,118960,118446,94137],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990571"},{"annotations":[116201,94138,113533,99448,104814,102114,114800,108135,101594,114087],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990813"},{"annotations":[72136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010032"},{"annotations":[71170],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051307"},{"annotations":[109957,90676,111437,109061,105198],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010780"},{"annotations":[78909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000707"},{"annotations":[110614,107976],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0010772"},{"annotations":[97250,101841,79263,88822,107977,100871,110615,117400],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000709"},{"annotations":[103594,111506],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140013"},{"annotations":[116359,106933,89400,114562],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0051598"},{"annotations":[94221,110492],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051755"},{"annotations":[104304,76794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051177"},{"annotations":[108136,117361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010789"},{"annotations":[70830,91262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051754"},{"annotations":[88345,111993,113534],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0045144"},{"annotations":[95107,97100],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0090306"},{"annotations":[75747,116966],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0033316"},{"annotations":[101754],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051232"},{"annotations":[99549,101755],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0140642"},{"annotations":[79386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000212"},{"annotations":[115425,94139],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1990395"},{"annotations":[100872,88823,79257],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010774"},{"annotations":[116244,117995,117859,97048],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0045141"},{"annotations":[114291],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0044821"},{"annotations":[100089,91633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061796"},{"annotations":[119505,119499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097753"},{"annotations":[60478,113954,69275,72523],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061025"},{"annotations":[71691,101983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061024"},{"annotations":[99018,100461],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1990949"},{"annotations":[100462,102606],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1990950"},{"annotations":[73404,78750,71077],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0007091"},{"annotations":[103365,97101,74374,99550],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990810"},{"annotations":[113073,97102,113083,118447,99551,97611,101756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001578"},{"annotations":[97612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062195"},{"annotations":[73223,77562,76481,93833,97906,104328,94185,77907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000226"},{"annotations":[118448,98947,89960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007019"},{"annotations":[72084,71500,79387],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007020"},{"annotations":[117243,101307,117488,100408,106766,100704],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0051415"},{"annotations":[118961,101308],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0051417"},{"annotations":[105190,104861],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0031023"},{"annotations":[95108,110215],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099606"},{"annotations":[79819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046785"},{"annotations":[96855,113084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051013"},{"annotations":[98501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090139"},{"annotations":[104334,107799,118648,104079,107486,72894,62066,59004,92826,89369,117352,107180,60733,94993,72362,78902,77090,95008,91993,97681,70620,89564,75971,102015],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0033617"},{"annotations":[90718],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032043"},{"annotations":[92903,102814,95071,97452,111893],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032042"},{"annotations":[103215,76706,112822,114206,99633,71564,103195,108868,96475],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043504"},{"annotations":[75209],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006264"},{"annotations":[99583,66966],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000266"},{"annotations":[72847,92278,96426],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008053"},{"annotations":[76748,96078,79563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000002"},{"annotations":[105227],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990627"},{"annotations":[108698,101609,112298],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1902775"},{"annotations":[103080,102822,95305],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0090149"},{"annotations":[107961,113324,93384,96952,109821,118149,107835,101604,106529,104703,106171,102533],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007006"},{"annotations":[59100,70318],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0070096"},{"annotations":[93615,101419,97653,107278],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035694"},{"annotations":[78451,110033,73850,110453,89385,74491],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0033615"},{"annotations":[95009,102878],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0097250"},{"annotations":[71123,67510,99575,107803],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0034553"},{"annotations":[78643,107908,113157,60595,77200],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0034551"},{"annotations":[95833,111832,102389,105024,98976,96270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070126"},{"annotations":[103081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000001"},{"annotations":[77922,72737,77586,80579,107070,107793,101215,75219,74289,91219,75929,77440,72603,111185,88586],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007005"},{"annotations":[70314,116911,80429,75123,70231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990456"},{"annotations":[112611,118177,92882,92932,99225,88600,98052,75289,119816,118761,98248,72899,102881,95622,112176,102738,76703,97977,75940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903475"},{"annotations":[77783],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1903479"},{"annotations":[101023,98358,112612,95623,99226,102739,118178,97978,88601,101251],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902404"},{"annotations":[111994,88346],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990893"},{"annotations":[70826,118008,77117,92131,98084,72134,72446,113691,104951,106514],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007076"},{"annotations":[100705,104212,108571],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007079"},{"annotations":[99614,108929,106446,113381,104983,102960,80778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140278"},{"annotations":[72394,78537,57521],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902977"},{"annotations":[108572,94535,98948,99554,104213],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990942"},{"annotations":[94177,101758],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0140515"},{"annotations":[98683,98013,110221,110634,93399,88235],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0101026"},{"annotations":[110772],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007077"},{"annotations":[119891,119455,119763],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0101024"},{"annotations":[96296,119918,91683,106879,98285,103462,119916,101210,119917,119919],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007084"},{"annotations":[103980],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0140516"},{"annotations":[103638,110872,115325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902985"},{"annotations":[100844,113535,114400,110201,118989,114801,117213,78346,90086,104214,103860,108573,89702,98950,102753,112926,94536,89482,112925,94172,99449,107817,109199,91320,112927],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990758"},{"annotations":[70872,104305,70190,88498,110863,72356,108052,57518,62845,101158,71185,67354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007064"},{"annotations":[91264,99450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071962"},{"annotations":[94639,96576,109455,109525,113858,117165,114439,105870,91119,116225,95034,112201,71733,114867,62521,106683,112490],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000070"},{"annotations":[102156,92094,101120,90686,95502,117878],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051306"},{"annotations":[97202,101309,110895,109919,118962],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0090307"},{"annotations":[99758,110216,114802,115857,106638,102116],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0007094"},{"annotations":[75853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051228"},{"annotations":[118963,107740,118450],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000022"},{"annotations":[95109,100707,103862],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0061805"},{"annotations":[108576,101760,97614,100708,98951,100181,104217],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0061804"},{"annotations":[99556,101761],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0140641"},{"annotations":[109170,95111,99557,97615,77543],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0051256"},{"annotations":[72060,76123,98600,114251,73660,76428,77399,88101,98131,112438],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007052"},{"annotations":[90469,107741,115426,113147,112945],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1903087"},{"annotations":[98601],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1905047"},{"annotations":[73488,101568],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000389"},{"annotations":[91905,98163,110939,95264,112674,102865,115548,106201,94340,95517,103026,95936,113583,110953,79907,110378],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000395"},{"annotations":[119016],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000348"},{"annotations":[77628,74608],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006376"},{"annotations":[74769],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0034496"},{"annotations":[75801],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010257"},{"annotations":[74791],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0034316"},{"annotations":[102678],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902424"},{"annotations":[91065],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051517"},{"annotations":[98602],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2000432"},{"annotations":[94916],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045806"},{"annotations":[93545,97546,93584,97656,103434,114449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045814"},{"annotations":[118248],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905560"},{"annotations":[99019],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902103"},{"annotations":[116604],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0090258"},{"annotations":[102365,106772],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0010637"},{"annotations":[102683],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903500"},{"annotations":[103595],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:2000816"},{"annotations":[94537],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[102688],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905757"},{"annotations":[77632,106970],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0061188"},{"annotations":[108284],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0045128"},{"annotations":[108806],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0060906"},{"annotations":[107548,110479,91066,73126,105363,99916,92071,101595,95972,116203,93185,93269,107854,93803,107413],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0031030"},{"annotations":[92080,106897,115639,106675,107718,106579],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045875"},{"annotations":[101773],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0061192"},{"annotations":[75472,71023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000280"},{"annotations":[78539,119460,92072,113053],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006998"},{"annotations":[70944,91684],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0071765"},{"annotations":[78993],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0048288"},{"annotations":[103776,92284,110039,119438,108033],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0071763"},{"annotations":[72522],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0031468"},{"annotations":[108077],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051292"},{"annotations":[76460,77331,80689,76750,74417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006999"},{"annotations":[96779,70228,73422,79189,91455,73565,114844,108044,91453],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006334"},{"annotations":[97416,90406,117201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006337"},{"annotations":[111579,113910,113599,75185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034728"},{"annotations":[109294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006294"},{"annotations":[80676],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071562"},{"annotations":[75449,80166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048284"},{"annotations":[59147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007008"},{"annotations":[77001,72116,76309,113192,73498,92893,74678],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033962"},{"annotations":[94419,98580,92412,72555,111580,108472,112928,112929,103095,104408,90552,103542,112930,114292,112414,113600,93168,114724,93789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031508"},{"annotations":[91686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140462"},{"annotations":[99584,92543,78093,78837],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0016559"},{"annotations":[107007],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045033"},{"annotations":[103082,100285,118474,80533],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007031"},{"annotations":[90860,90865,60040,75138,90864,101605,90859,74880,90857,102534,90863,109822,72480,73371,99799,90862,62827,73209,90858,90861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045332"},{"annotations":[92694,78233,95626,96702,110504],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0032220"},{"annotations":[114985,92240,104695,90752,90497,104192,111075,117831,118144,118763],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007009"},{"annotations":[73547],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0017121"},{"annotations":[72409,74322],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0097320"},{"annotations":[108579,104219],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070462"},{"annotations":[91067],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903024"},{"annotations":[116309,105502,112268],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902425"},{"annotations":[108969,108879],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2000786"},{"annotations":[97951],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1901098"},{"annotations":[106971],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0030307"},{"annotations":[94141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045793"},{"annotations":[104015],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045807"},{"annotations":[64749],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903373"},{"annotations":[99289],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0031453"},{"annotations":[89990,116972,102692],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905561"},{"annotations":[90208,111673,88236,91187,93822],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902917"},{"annotations":[88556,106017],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2001178"},{"annotations":[114090],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[108672,102694],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905263"},{"annotations":[95494],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905191"},{"annotations":[102169],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0031117"},{"annotations":[96079],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090297"},{"annotations":[109194],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090141"},{"annotations":[90339,94748],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903501"},{"annotations":[87876,113669,94917,94749,110834],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903473"},{"annotations":[116973],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[116974,102696],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903380"},{"annotations":[90209,105503,106703,94144,78274,118190,92759,115772,107364,113670],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140281"},{"annotations":[100463,94145,102426,115071,98025,102697,111683],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045842"},{"annotations":[94146,102698,111511,116976,90341],"is_not":false,"rel_names":["regulates","part_of"],"summary":null,"term":"GO:0140429"},{"annotations":[94750,90342],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902846"},{"annotations":[111744],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0110161"},{"annotations":[91524],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090053"},{"annotations":[94752,87877,92760],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905758"},{"annotations":[89402],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0010845"},{"annotations":[79924,90049],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045899"},{"annotations":[102702,110835,87878,94148,90343],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0031031"},{"annotations":[91525,94710,110656],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090055"},{"annotations":[107720],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045876"},{"annotations":[97515],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0032215"},{"annotations":[112271],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1904595"},{"annotations":[76834,68832,66593],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045905"},{"annotations":[97952,110578],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0061191"},{"annotations":[74582,70161,75822,70745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000973"},{"annotations":[114687,106430],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031671"},{"annotations":[90073,100474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030994"},{"annotations":[104659,57408,62620,59559,58317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043248"},{"annotations":[80374,99810,116036],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070682"},{"annotations":[80144,90106],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031848"},{"annotations":[105320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140454"},{"annotations":[73720,79901,71073,111699,70376,102581,72298,96804],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016558"},{"annotations":[70945,74152,62738],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016560"},{"annotations":[98898,115602,64249,117606],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016562"},{"annotations":[95761,90767,111700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045046"},{"annotations":[110712,114693,114141,106491,109648,68254,95167,108625,104798,105104,98919,92006,101513,71777,103828,98377,98690,112559,108714],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045048"},{"annotations":[90731,107903,88997,78224,75972,73837,74345,116567,113501,103239,107881],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[78644,58339,78903,74790,78854],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032979"},{"annotations":[107882,70313,59099,98557,112101,98908,76946,110710,110357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045040"},{"annotations":[97203,91636,114236],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902441"},{"annotations":[103410,97289,90776,90768,95762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006625"},{"annotations":[74352,75035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0022618"},{"annotations":[71174,92413,112415,72553,108473,104409,113601],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000183"},{"annotations":[93021,91145,71443,100907,100970,78198,93094,89936,115839,101465,69631,104645,104185,105162,91811,107042,79593],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007131"},{"annotations":[104743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045458"},{"annotations":[71853,96189,73704,78249,79286,99771,103160,110414,115620,78086,116784,73730,74424],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032956"},{"annotations":[107927],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032231"},{"annotations":[76970,68426,67297,77641,79783],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0030833"},{"annotations":[117227],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903023"},{"annotations":[115350],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051516"},{"annotations":[94881],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008361"},{"annotations":[111332,111977,119155],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000369"},{"annotations":[71690,76549],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0003400"},{"annotations":[78580,88238,75753],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032955"},{"annotations":[90212,92765,113671,93052,113541,77858,91303,103249,78694],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0030100"},{"annotations":[98758],"is_not":false,"rel_names":["regulates","part_of"],"summary":null,"term":"GO:0061387"},{"annotations":[111292,71916,87935],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0060237"},{"annotations":[91152,98893],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0031445"},{"annotations":[110495,94226],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090006"},{"annotations":[102708],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0062123"},{"annotations":[101658],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"},{"annotations":[97270],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0040020"},{"annotations":[113353,100505,105683,115621,91481,104021],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0070507"},{"annotations":[70973],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0031110"},{"annotations":[90154],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010821"},{"annotations":[94150,119900],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903499"},{"annotations":[111238],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0007088"},{"annotations":[94178,103983],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905557"},{"annotations":[71909],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1901673"},{"annotations":[115352],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0110162"},{"annotations":[90213],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0060236"},{"annotations":[97516,100624],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090052"},{"annotations":[101522,72331],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0097036"},{"annotations":[118053],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010964"},{"annotations":[103543],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902681"},{"annotations":[92203,118417,97517,118054,100625],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902801"},{"annotations":[101159],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0007063"},{"annotations":[116979],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904967"},{"annotations":[77245],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032210"},{"annotations":[74429],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006449"},{"annotations":[97717],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032889"},{"annotations":[113360,104410,108094,109430,107667,112165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031048"},{"annotations":[115326,102595,99688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031582"},{"annotations":[103447,76964,78567,105960,64520,70206,75723,116388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072344"},{"annotations":[74776,108461,79538,77043,117596,109396,110638,72050,75313,117746],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000712"},{"annotations":[72545,72682,71461,73158,66310],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000027"},{"annotations":[75086,76937,77014,77442,70196,70366,73616,75579,72964,118906,75095,73784,74870,74021,90274,95095,72110,77583,74953,72307],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000028"},{"annotations":[109019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042255"},{"annotations":[71027,105025,103927,74890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032790"},{"annotations":[74271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904802"},{"annotations":[118359,78877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990113"},{"annotations":[64205,68843,77879],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001188"},{"annotations":[78878,118360,102516],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990114"},{"annotations":[74047,94482,72297,77206,71706,75296,67585,70861,71057,74844,75967,77612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051123"},{"annotations":[118361,78879],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990115"},{"annotations":[103385,72161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070898"},{"annotations":[72185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010265"},{"annotations":[116120],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990344"},{"annotations":[110999],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032185"},{"annotations":[72786,100441,104238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000921"},{"annotations":[70528,98148,102086,117333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031106"},{"annotations":[116285,104411,111518,117996,119114,108474,118394,113976,99890,110797,94420,99453,95854,111581,113602,103545,114294,91612,108288,72000,112517,93096,104507,97061,112416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030466"},{"annotations":[116834,110798,104508,87839,91135,112417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902794"},{"annotations":[106629],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902795"},{"annotations":[114295],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141194"},{"annotations":[110799,117997,118282,116287,119115,91613,99454,111519,94432,114873,118396,95673,97062,106868,89119,113977,114609,110965,115725,89175,99892,112518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140727"},{"annotations":[109456],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031134"},{"annotations":[113374,73350],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0034462"},{"annotations":[76014],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0035493"},{"annotations":[57482,76736],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035494"},{"annotations":[116534],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0062209"},{"annotations":[106768,100410,117490,78631,70975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051225"},{"annotations":[114402,91322,89484,98954,110628,100846,101659,107819,109457,98233,110671,117215,105801,116226,94151,90088,102754,113536,95647,95893,108137,109201,110203],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051455"},{"annotations":[89986,95707],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0051300"},{"annotations":[76356,79309,93721,76027,74256,72724,105814,102060,72466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000245"},{"annotations":[88119,104835,78898,75303,57266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000390"},{"annotations":[98341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000393"},{"annotations":[89816,73066,76035,79676,96312,115419,109299,97172,104871,113584,62522,65438,72118,77447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000387"},{"annotations":[106869,76420,112556,63407,72933,114690,105815,78029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000244"},{"annotations":[100957],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000388"},{"annotations":[116271,100161,94841,100162,106335,100442],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0070583"},{"annotations":[114671,91969,115432],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006617"},{"annotations":[113632,73499,77002,72897,79296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034063"},{"annotations":[60753,65906,67067,59443],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061753"},{"annotations":[111582,92415,103546,110800,113978,117998,118397,91614,97063,90553,98581,119116,60053,90395,104412,104509,114296,99455,94421,112418,113603,108475],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031509"},{"annotations":[73194,75401,114432],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071816"},{"annotations":[65159,108246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904868"},{"annotations":[106667,115241,116706,116171,96161,108857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905323"},{"annotations":[92175,77241,63418,100047,116245,110683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016233"},{"annotations":[109691,79770,106280,71310,116556,104475,79162,113134,111840,70690,78605,117148,58925,91773,109869,72047,99390,99518,108349,101182,89463,108069,71934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000723"},{"annotations":[112042,113251,113253,113249,96514,113250,113252,80598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000722"},{"annotations":[114128,108431,80596,70938,90979,80638,116247,69965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007004"},{"annotations":[80141,92177,74513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010833"},{"annotations":[108432,100050,116248],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1905324"},{"annotations":[116510,94947,113911,93735,109097,114846,119143,111583,92720,95815,109092,90407,103879,91580,117202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140673"},{"annotations":[88832,109656,94472,104166,94458,93857,107756,109888,115312,95782,99467,88683,103096,88500,89451,98149,112061,117751,97418,107219,114526,116835,101881,105347,96780,110921,117914,98994,91049,106096,117866,94350,114701,90408,107995,91035,89624,90930,94120,94645,93136,104885,109379,113625,115689,88145,99717,108779,110786,103435,115703,96983,113435,96226,105355,116005,114537,113281,94548,114610,118265,89216,90136,108193,103682,105947,107643,117203,116587,88323,94979,101296,94520,98828,107067,116648,91751,92636,113454,115021,87998,94492,115557,117568,112857,98562,96219,117844,109780,95807],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045815"},{"annotations":[80772,75514,73996,77070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000972"},{"annotations":[77870,62187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006415"},{"annotations":[116836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141005"},{"annotations":[93608,97089,106566,71120,65498,88929,67410,93835,96886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007021"},{"annotations":[107082,114155,112756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903241"},{"annotations":[64294,116846,67613,102302,64093,110472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070072"},{"annotations":[103083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140572"},{"annotations":[94658,116482,99840,117852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097576"},{"annotations":[91511,101076,71511,104958,108594,109739,117125,100286,100578,101444,91637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042144"},{"annotations":[99014,96469,75447,73649,80164,107941,72940,92362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007033"},{"annotations":[107345,115505],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990854"},{"annotations":[74036,70369,71115,79613,76641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006900"},{"annotations":[95851],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006901"},{"annotations":[112993,117809,117854,78366,90919,98424,78072,109966,101175,76558,76923,72371,101402],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006906"},{"annotations":[78120,57752,76518,74246],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0048280"},{"annotations":[100287],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099050"},{"annotations":[118734],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099022"},{"annotations":[99875,60327,91087,118026,66289,88964,102240,114461],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090522"}]},"cv_name":"biological_process","definition":"A process that results in the assembly, arrangement of constituent parts, or disassembly of a cellular component.","definition_xrefs":["GOC:mah","GOC:jl","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component organization or biogenesis","termid":"GO:0071840"}],"gene_count":1396,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00018":null,"SJAG_00029":null,"SJAG_00030":null,"SJAG_00031":null,"SJAG_00045":null,"SJAG_00053":null,"SJAG_00058":null,"SJAG_00064":null,"SJAG_00066":null,"SJAG_00072":null,"SJAG_00078":null,"SJAG_00079":null,"SJAG_00082":null,"SJAG_00087":null,"SJAG_00100":null,"SJAG_00113":null,"SJAG_00114":null,"SJAG_00118":null,"SJAG_00126":null,"SJAG_00140":null,"SJAG_00142":null,"SJAG_00145":null,"SJAG_00146":null,"SJAG_00147":null,"SJAG_00152":null,"SJAG_00153":null,"SJAG_00154":null,"SJAG_00160":null,"SJAG_00163":null,"SJAG_00168":null,"SJAG_00170":null,"SJAG_00171":null,"SJAG_00172":null,"SJAG_00184":null,"SJAG_00185":null,"SJAG_00186":null,"SJAG_00187":null,"SJAG_00188":null,"SJAG_00198":null,"SJAG_00204":null,"SJAG_00206":null,"SJAG_00207":null,"SJAG_00216":null,"SJAG_00217":null,"SJAG_00218":null,"SJAG_00225":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00230":null,"SJAG_00231":null,"SJAG_00244":null,"SJAG_00247":null,"SJAG_00249":null,"SJAG_00259":null,"SJAG_00261":null,"SJAG_00266":null,"SJAG_00268":null,"SJAG_00277":null,"SJAG_00278":null,"SJAG_00279":null,"SJAG_00284":null,"SJAG_00286":null,"SJAG_00293":null,"SJAG_00298":null,"SJAG_00301":null,"SJAG_00302":null,"SJAG_00303":null,"SJAG_00304":null,"SJAG_00307":null,"SJAG_00308":null,"SJAG_00313":null,"SJAG_00320":null,"SJAG_00322":null,"SJAG_00323":null,"SJAG_00326":null,"SJAG_00327":null,"SJAG_00330":null,"SJAG_00333":null,"SJAG_00335":null,"SJAG_00336":null,"SJAG_00338":null,"SJAG_00341":null,"SJAG_00349":null,"SJAG_00350":null,"SJAG_00353":null,"SJAG_00354":null,"SJAG_00355":null,"SJAG_00357":null,"SJAG_00364":null,"SJAG_00368":null,"SJAG_00369":null,"SJAG_00377":null,"SJAG_00380":null,"SJAG_00397":null,"SJAG_00402":null,"SJAG_00404":null,"SJAG_00405":null,"SJAG_00411":null,"SJAG_00414":null,"SJAG_00416":null,"SJAG_00418":null,"SJAG_00424":null,"SJAG_00429":null,"SJAG_00430":null,"SJAG_00433":null,"SJAG_00436":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00442":null,"SJAG_00449":null,"SJAG_00455":null,"SJAG_00460":null,"SJAG_00466":null,"SJAG_00474":null,"SJAG_00476":null,"SJAG_00486":null,"SJAG_00496":null,"SJAG_00498":null,"SJAG_00505":null,"SJAG_00510":null,"SJAG_00513":null,"SJAG_00514":null,"SJAG_00521":null,"SJAG_00523":null,"SJAG_00526":null,"SJAG_00532":null,"SJAG_00545":null,"SJAG_00551":null,"SJAG_00557":null,"SJAG_00559":null,"SJAG_00564":null,"SJAG_00569":null,"SJAG_00572":null,"SJAG_00576":null,"SJAG_00578":null,"SJAG_00581":null,"SJAG_00584":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00594":null,"SJAG_00596":null,"SJAG_00597":null,"SJAG_00600":null,"SJAG_00603":null,"SJAG_00610":null,"SJAG_00611":null,"SJAG_00618":null,"SJAG_00623":null,"SJAG_00634":null,"SJAG_00638":null,"SJAG_00640":null,"SJAG_00641":null,"SJAG_00642":null,"SJAG_00643":null,"SJAG_00645":null,"SJAG_00646":null,"SJAG_00649":null,"SJAG_00661":null,"SJAG_00662":null,"SJAG_00663":null,"SJAG_00666":null,"SJAG_00667":null,"SJAG_00669":null,"SJAG_00676":null,"SJAG_00677":null,"SJAG_00678":null,"SJAG_00680":null,"SJAG_00682":null,"SJAG_00684":null,"SJAG_00687":null,"SJAG_00689":null,"SJAG_00692":null,"SJAG_00697":null,"SJAG_00700":null,"SJAG_00701":null,"SJAG_00702":null,"SJAG_00703":null,"SJAG_00718":null,"SJAG_00719":null,"SJAG_00722":null,"SJAG_00723":null,"SJAG_00727":null,"SJAG_00735":null,"SJAG_00739":null,"SJAG_00741":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00752":null,"SJAG_00756":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00768":null,"SJAG_00769":null,"SJAG_00771":null,"SJAG_00773":null,"SJAG_00783":null,"SJAG_00794":null,"SJAG_00796":null,"SJAG_00806":null,"SJAG_00810":null,"SJAG_00821":null,"SJAG_00823":null,"SJAG_00826":null,"SJAG_00840":null,"SJAG_00845":null,"SJAG_00852":null,"SJAG_00855":null,"SJAG_00856":null,"SJAG_00858":null,"SJAG_00859":null,"SJAG_00868":null,"SJAG_00870":null,"SJAG_00871":null,"SJAG_00873":null,"SJAG_00882":null,"SJAG_00883":null,"SJAG_00891":null,"SJAG_00894":null,"SJAG_00896":null,"SJAG_00898":null,"SJAG_00899":null,"SJAG_00900":null,"SJAG_00906":null,"SJAG_00907":null,"SJAG_00908":null,"SJAG_00911":null,"SJAG_00912":null,"SJAG_00913":null,"SJAG_00914":null,"SJAG_00918":null,"SJAG_00925":null,"SJAG_00930":null,"SJAG_00934":null,"SJAG_00935":null,"SJAG_00938":null,"SJAG_00939":null,"SJAG_00942":null,"SJAG_00943":null,"SJAG_00949":null,"SJAG_00954":null,"SJAG_00959":null,"SJAG_00961":null,"SJAG_00970":null,"SJAG_00971":null,"SJAG_00972":null,"SJAG_00973":null,"SJAG_00974":null,"SJAG_00980":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_01003":null,"SJAG_01005":null,"SJAG_01008":null,"SJAG_01009":null,"SJAG_01015":null,"SJAG_01016":null,"SJAG_01017":null,"SJAG_01044":null,"SJAG_01046":null,"SJAG_01048":null,"SJAG_01050":null,"SJAG_01063":null,"SJAG_01067":null,"SJAG_01068":null,"SJAG_01072":null,"SJAG_01073":null,"SJAG_01074":null,"SJAG_01075":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01095":null,"SJAG_01110":null,"SJAG_01111":null,"SJAG_01114":null,"SJAG_01116":null,"SJAG_01120":null,"SJAG_01122":null,"SJAG_01127":null,"SJAG_01138":null,"SJAG_01140":null,"SJAG_01141":null,"SJAG_01143":null,"SJAG_01146":null,"SJAG_01152":null,"SJAG_01156":null,"SJAG_01161":null,"SJAG_01165":null,"SJAG_01168":null,"SJAG_01169":null,"SJAG_01171":null,"SJAG_01178":null,"SJAG_01180":null,"SJAG_01181":null,"SJAG_01188":null,"SJAG_01193":null,"SJAG_01200":null,"SJAG_01204":null,"SJAG_01207":null,"SJAG_01211":null,"SJAG_01212":null,"SJAG_01214":null,"SJAG_01215":null,"SJAG_01217":null,"SJAG_01223":null,"SJAG_01224":null,"SJAG_01225":null,"SJAG_01227":null,"SJAG_01228":null,"SJAG_01229":null,"SJAG_01230":null,"SJAG_01233":null,"SJAG_01238":null,"SJAG_01240":null,"SJAG_01242":null,"SJAG_01251":null,"SJAG_01252":null,"SJAG_01262":null,"SJAG_01263":null,"SJAG_01268":null,"SJAG_01270":null,"SJAG_01274":null,"SJAG_01278":null,"SJAG_01282":null,"SJAG_01283":null,"SJAG_01290":null,"SJAG_01296":null,"SJAG_01297":null,"SJAG_01299":null,"SJAG_01301":null,"SJAG_01305":null,"SJAG_01315":null,"SJAG_01317":null,"SJAG_01320":null,"SJAG_01321":null,"SJAG_01324":null,"SJAG_01325":null,"SJAG_01327":null,"SJAG_01329":null,"SJAG_01330":null,"SJAG_01331":null,"SJAG_01339":null,"SJAG_01356":null,"SJAG_01357":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01373":null,"SJAG_01374":null,"SJAG_01377":null,"SJAG_01378":null,"SJAG_01379":null,"SJAG_01384":null,"SJAG_01385":null,"SJAG_01386":null,"SJAG_01388":null,"SJAG_01405":null,"SJAG_01407":null,"SJAG_01410":null,"SJAG_01417":null,"SJAG_01419":null,"SJAG_01420":null,"SJAG_01422":null,"SJAG_01437":null,"SJAG_01440":null,"SJAG_01448":null,"SJAG_01453":null,"SJAG_01454":null,"SJAG_01456":null,"SJAG_01459":null,"SJAG_01460":null,"SJAG_01464":null,"SJAG_01465":null,"SJAG_01467":null,"SJAG_01470":null,"SJAG_01475":null,"SJAG_01483":null,"SJAG_01487":null,"SJAG_01497":null,"SJAG_01503":null,"SJAG_01504":null,"SJAG_01511":null,"SJAG_01513":null,"SJAG_01515":null,"SJAG_01516":null,"SJAG_01518":null,"SJAG_01523":null,"SJAG_01526":null,"SJAG_01530":null,"SJAG_01537":null,"SJAG_01538":null,"SJAG_01540":null,"SJAG_01545":null,"SJAG_01546":null,"SJAG_01547":null,"SJAG_01548":null,"SJAG_01561":null,"SJAG_01564":null,"SJAG_01567":null,"SJAG_01568":null,"SJAG_01571":null,"SJAG_01579":null,"SJAG_01590":null,"SJAG_01594":null,"SJAG_01598":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01605":null,"SJAG_01606":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01622":null,"SJAG_01633":null,"SJAG_01640":null,"SJAG_01644":null,"SJAG_01648":null,"SJAG_01652":null,"SJAG_01653":null,"SJAG_01654":null,"SJAG_01658":null,"SJAG_01662":null,"SJAG_01665":null,"SJAG_01675":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01685":null,"SJAG_01696":null,"SJAG_01697":null,"SJAG_01707":null,"SJAG_01708":null,"SJAG_01711":null,"SJAG_01713":null,"SJAG_01716":null,"SJAG_01722":null,"SJAG_01731":null,"SJAG_01732":null,"SJAG_01741":null,"SJAG_01745":null,"SJAG_01748":null,"SJAG_01756":null,"SJAG_01759":null,"SJAG_01760":null,"SJAG_01761":null,"SJAG_01769":null,"SJAG_01771":null,"SJAG_01772":null,"SJAG_01774":null,"SJAG_01775":null,"SJAG_01777":null,"SJAG_01780":null,"SJAG_01782":null,"SJAG_01785":null,"SJAG_01790":null,"SJAG_01794":null,"SJAG_01804":null,"SJAG_01805":null,"SJAG_01807":null,"SJAG_01808":null,"SJAG_01811":null,"SJAG_01816":null,"SJAG_01819":null,"SJAG_01821":null,"SJAG_01823":null,"SJAG_01825":null,"SJAG_01826":null,"SJAG_01831":null,"SJAG_01832":null,"SJAG_01833":null,"SJAG_01834":null,"SJAG_01835":null,"SJAG_01836":null,"SJAG_01837":null,"SJAG_01838":null,"SJAG_01839":null,"SJAG_01848":null,"SJAG_01863":null,"SJAG_01864":null,"SJAG_01867":null,"SJAG_01870":null,"SJAG_01873":null,"SJAG_01876":null,"SJAG_01878":null,"SJAG_01888":null,"SJAG_01894":null,"SJAG_01895":null,"SJAG_01896":null,"SJAG_01906":null,"SJAG_01912":null,"SJAG_01917":null,"SJAG_01925":null,"SJAG_01926":null,"SJAG_01928":null,"SJAG_01929":null,"SJAG_01938":null,"SJAG_01939":null,"SJAG_01940":null,"SJAG_01943":null,"SJAG_01945":null,"SJAG_01948":null,"SJAG_01949":null,"SJAG_01951":null,"SJAG_01956":null,"SJAG_01964":null,"SJAG_01992":null,"SJAG_01993":null,"SJAG_01996":null,"SJAG_01999":null,"SJAG_02002":null,"SJAG_02019":null,"SJAG_02028":null,"SJAG_02034":null,"SJAG_02035":null,"SJAG_02040":null,"SJAG_02045":null,"SJAG_02058":null,"SJAG_02064":null,"SJAG_02065":null,"SJAG_02066":null,"SJAG_02074":null,"SJAG_02075":null,"SJAG_02079":null,"SJAG_02081":null,"SJAG_02087":null,"SJAG_02096":null,"SJAG_02100":null,"SJAG_02104":null,"SJAG_02114":null,"SJAG_02116":null,"SJAG_02119":null,"SJAG_02120":null,"SJAG_02132":null,"SJAG_02164":null,"SJAG_02165":null,"SJAG_02166":null,"SJAG_02169":null,"SJAG_02170":null,"SJAG_02174":null,"SJAG_02177":null,"SJAG_02181":null,"SJAG_02184":null,"SJAG_02185":null,"SJAG_02186":null,"SJAG_02187":null,"SJAG_02189":null,"SJAG_02192":null,"SJAG_02194":null,"SJAG_02198":null,"SJAG_02202":null,"SJAG_02204":null,"SJAG_02208":null,"SJAG_02210":null,"SJAG_02212":null,"SJAG_02213":null,"SJAG_02215":null,"SJAG_02222":null,"SJAG_02226":null,"SJAG_02228":null,"SJAG_02229":null,"SJAG_02241":null,"SJAG_02245":null,"SJAG_02246":null,"SJAG_02248":null,"SJAG_02254":null,"SJAG_02263":null,"SJAG_02265":null,"SJAG_02267":null,"SJAG_02270":null,"SJAG_02279":null,"SJAG_02286":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02303":null,"SJAG_02304":null,"SJAG_02306":null,"SJAG_02311":null,"SJAG_02314":null,"SJAG_02315":null,"SJAG_02319":null,"SJAG_02320":null,"SJAG_02323":null,"SJAG_02329":null,"SJAG_02330":null,"SJAG_02332":null,"SJAG_02335":null,"SJAG_02336":null,"SJAG_02338":null,"SJAG_02339":null,"SJAG_02340":null,"SJAG_02342":null,"SJAG_02346":null,"SJAG_02347":null,"SJAG_02348":null,"SJAG_02349":null,"SJAG_02350":null,"SJAG_02351":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_02362":null,"SJAG_02366":null,"SJAG_02373":null,"SJAG_02375":null,"SJAG_02376":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02381":null,"SJAG_02382":null,"SJAG_02384":null,"SJAG_02385":null,"SJAG_02390":null,"SJAG_02392":null,"SJAG_02394":null,"SJAG_02398":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02414":null,"SJAG_02416":null,"SJAG_02427":null,"SJAG_02431":null,"SJAG_02433":null,"SJAG_02436":null,"SJAG_02437":null,"SJAG_02439":null,"SJAG_02441":null,"SJAG_02446":null,"SJAG_02447":null,"SJAG_02451":null,"SJAG_02455":null,"SJAG_02456":null,"SJAG_02457":null,"SJAG_02458":null,"SJAG_02460":null,"SJAG_02465":null,"SJAG_02466":null,"SJAG_02469":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02480":null,"SJAG_02490":null,"SJAG_02497":null,"SJAG_02498":null,"SJAG_02500":null,"SJAG_02501":null,"SJAG_02508":null,"SJAG_02509":null,"SJAG_02511":null,"SJAG_02513":null,"SJAG_02514":null,"SJAG_02516":null,"SJAG_02524":null,"SJAG_02528":null,"SJAG_02529":null,"SJAG_02532":null,"SJAG_02535":null,"SJAG_02539":null,"SJAG_02541":null,"SJAG_02542":null,"SJAG_02549":null,"SJAG_02551":null,"SJAG_02556":null,"SJAG_02558":null,"SJAG_02560":null,"SJAG_02561":null,"SJAG_02563":null,"SJAG_02566":null,"SJAG_02570":null,"SJAG_02571":null,"SJAG_02573":null,"SJAG_02576":null,"SJAG_02581":null,"SJAG_02587":null,"SJAG_02589":null,"SJAG_02590":null,"SJAG_02592":null,"SJAG_02594":null,"SJAG_02595":null,"SJAG_02601":null,"SJAG_02606":null,"SJAG_02607":null,"SJAG_02609":null,"SJAG_02613":null,"SJAG_02616":null,"SJAG_02619":null,"SJAG_02621":null,"SJAG_02622":null,"SJAG_02624":null,"SJAG_02626":null,"SJAG_02628":null,"SJAG_02629":null,"SJAG_02638":null,"SJAG_02640":null,"SJAG_02645":null,"SJAG_02649":null,"SJAG_02651":null,"SJAG_02652":null,"SJAG_02656":null,"SJAG_02658":null,"SJAG_02659":null,"SJAG_02663":null,"SJAG_02664":null,"SJAG_02667":null,"SJAG_02672":null,"SJAG_02683":null,"SJAG_02684":null,"SJAG_02691":null,"SJAG_02693":null,"SJAG_02695":null,"SJAG_02698":null,"SJAG_02699":null,"SJAG_02700":null,"SJAG_02701":null,"SJAG_02704":null,"SJAG_02707":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02718":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02726":null,"SJAG_02731":null,"SJAG_02733":null,"SJAG_02736":null,"SJAG_02737":null,"SJAG_02746":null,"SJAG_02748":null,"SJAG_02749":null,"SJAG_02754":null,"SJAG_02756":null,"SJAG_02757":null,"SJAG_02759":null,"SJAG_02761":null,"SJAG_02763":null,"SJAG_02768":null,"SJAG_02771":null,"SJAG_02773":null,"SJAG_02778":null,"SJAG_02788":null,"SJAG_02795":null,"SJAG_02797":null,"SJAG_02798":null,"SJAG_02803":null,"SJAG_02807":null,"SJAG_02812":null,"SJAG_02813":null,"SJAG_02814":null,"SJAG_02817":null,"SJAG_02822":null,"SJAG_02830":null,"SJAG_02831":null,"SJAG_02838":null,"SJAG_02840":null,"SJAG_02843":null,"SJAG_02845":null,"SJAG_02846":null,"SJAG_02848":null,"SJAG_02864":null,"SJAG_02866":null,"SJAG_02868":null,"SJAG_02869":null,"SJAG_02870":null,"SJAG_02872":null,"SJAG_02873":null,"SJAG_02878":null,"SJAG_02886":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02906":null,"SJAG_02908":null,"SJAG_02914":null,"SJAG_02915":null,"SJAG_02916":null,"SJAG_02924":null,"SJAG_02927":null,"SJAG_02943":null,"SJAG_02952":null,"SJAG_02957":null,"SJAG_02975":null,"SJAG_02979":null,"SJAG_02980":null,"SJAG_02981":null,"SJAG_02989":null,"SJAG_02990":null,"SJAG_02994":null,"SJAG_02995":null,"SJAG_02997":null,"SJAG_03005":null,"SJAG_03006":null,"SJAG_03007":null,"SJAG_03011":null,"SJAG_03012":null,"SJAG_03013":null,"SJAG_03023":null,"SJAG_03025":null,"SJAG_03026":null,"SJAG_03033":null,"SJAG_03036":null,"SJAG_03038":null,"SJAG_03041":null,"SJAG_03042":null,"SJAG_03044":null,"SJAG_03045":null,"SJAG_03046":null,"SJAG_03047":null,"SJAG_03048":null,"SJAG_03050":null,"SJAG_03052":null,"SJAG_03062":null,"SJAG_03068":null,"SJAG_03070":null,"SJAG_03072":null,"SJAG_03073":null,"SJAG_03080":null,"SJAG_03086":null,"SJAG_03088":null,"SJAG_03090":null,"SJAG_03092":null,"SJAG_03095":null,"SJAG_03099":null,"SJAG_03100":null,"SJAG_03106":null,"SJAG_03116":null,"SJAG_03118":null,"SJAG_03119":null,"SJAG_03120":null,"SJAG_03123":null,"SJAG_03125":null,"SJAG_03126":null,"SJAG_03128":null,"SJAG_03137":null,"SJAG_03145":null,"SJAG_03146":null,"SJAG_03147":null,"SJAG_03153":null,"SJAG_03155":null,"SJAG_03157":null,"SJAG_03161":null,"SJAG_03162":null,"SJAG_03168":null,"SJAG_03170":null,"SJAG_03172":null,"SJAG_03182":null,"SJAG_03183":null,"SJAG_03189":null,"SJAG_03193":null,"SJAG_03200":null,"SJAG_03209":null,"SJAG_03214":null,"SJAG_03217":null,"SJAG_03219":null,"SJAG_03220":null,"SJAG_03221":null,"SJAG_03222":null,"SJAG_03229":null,"SJAG_03230":null,"SJAG_03232":null,"SJAG_03247":null,"SJAG_03250":null,"SJAG_03255":null,"SJAG_03264":null,"SJAG_03268":null,"SJAG_03270":null,"SJAG_03279":null,"SJAG_03282":null,"SJAG_03285":null,"SJAG_03286":null,"SJAG_03287":null,"SJAG_03295":null,"SJAG_03296":null,"SJAG_03299":null,"SJAG_03301":null,"SJAG_03313":null,"SJAG_03315":null,"SJAG_03322":null,"SJAG_03323":null,"SJAG_03324":null,"SJAG_03327":null,"SJAG_03337":null,"SJAG_03338":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03347":null,"SJAG_03353":null,"SJAG_03356":null,"SJAG_03357":null,"SJAG_03361":null,"SJAG_03366":null,"SJAG_03379":null,"SJAG_03380":null,"SJAG_03386":null,"SJAG_03387":null,"SJAG_03393":null,"SJAG_03394":null,"SJAG_03395":null,"SJAG_03399":null,"SJAG_03401":null,"SJAG_03403":null,"SJAG_03416":null,"SJAG_03418":null,"SJAG_03421":null,"SJAG_03424":null,"SJAG_03428":null,"SJAG_03431":null,"SJAG_03435":null,"SJAG_03437":null,"SJAG_03438":null,"SJAG_03440":null,"SJAG_03441":null,"SJAG_03444":null,"SJAG_03449":null,"SJAG_03453":null,"SJAG_03455":null,"SJAG_03456":null,"SJAG_03458":null,"SJAG_03460":null,"SJAG_03463":null,"SJAG_03464":null,"SJAG_03465":null,"SJAG_03466":null,"SJAG_03469":null,"SJAG_03472":null,"SJAG_03486":null,"SJAG_03487":null,"SJAG_03491":null,"SJAG_03493":null,"SJAG_03496":null,"SJAG_03502":null,"SJAG_03508":null,"SJAG_03515":null,"SJAG_03525":null,"SJAG_03536":null,"SJAG_03537":null,"SJAG_03540":null,"SJAG_03542":null,"SJAG_03543":null,"SJAG_03544":null,"SJAG_03546":null,"SJAG_03548":null,"SJAG_03551":null,"SJAG_03552":null,"SJAG_03558":null,"SJAG_03563":null,"SJAG_03567":null,"SJAG_03574":null,"SJAG_03575":null,"SJAG_03576":null,"SJAG_03579":null,"SJAG_03581":null,"SJAG_03591":null,"SJAG_03592":null,"SJAG_03593":null,"SJAG_03596":null,"SJAG_03599":null,"SJAG_03602":null,"SJAG_03603":null,"SJAG_03609":null,"SJAG_03617":null,"SJAG_03619":null,"SJAG_03624":null,"SJAG_03625":null,"SJAG_03627":null,"SJAG_03628":null,"SJAG_03630":null,"SJAG_03631":null,"SJAG_03633":null,"SJAG_03635":null,"SJAG_03637":null,"SJAG_03646":null,"SJAG_03655":null,"SJAG_03658":null,"SJAG_03664":null,"SJAG_03668":null,"SJAG_03670":null,"SJAG_03673":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03682":null,"SJAG_03683":null,"SJAG_03685":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03694":null,"SJAG_03698":null,"SJAG_03700":null,"SJAG_03701":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03705":null,"SJAG_03710":null,"SJAG_03718":null,"SJAG_03720":null,"SJAG_03721":null,"SJAG_03722":null,"SJAG_03724":null,"SJAG_03725":null,"SJAG_03741":null,"SJAG_03746":null,"SJAG_03748":null,"SJAG_03751":null,"SJAG_03752":null,"SJAG_03758":null,"SJAG_03773":null,"SJAG_03774":null,"SJAG_03776":null,"SJAG_03780":null,"SJAG_03781":null,"SJAG_03782":null,"SJAG_03783":null,"SJAG_03784":null,"SJAG_03787":null,"SJAG_03792":null,"SJAG_03795":null,"SJAG_03798":null,"SJAG_03812":null,"SJAG_03832":null,"SJAG_03835":null,"SJAG_03839":null,"SJAG_03843":null,"SJAG_03844":null,"SJAG_03846":null,"SJAG_03848":null,"SJAG_03851":null,"SJAG_03855":null,"SJAG_03862":null,"SJAG_03864":null,"SJAG_03865":null,"SJAG_03867":null,"SJAG_03873":null,"SJAG_03884":null,"SJAG_03887":null,"SJAG_03889":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03894":null,"SJAG_03898":null,"SJAG_03900":null,"SJAG_03905":null,"SJAG_03906":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03916":null,"SJAG_03926":null,"SJAG_03930":null,"SJAG_03936":null,"SJAG_03938":null,"SJAG_03940":null,"SJAG_03941":null,"SJAG_03942":null,"SJAG_03944":null,"SJAG_03945":null,"SJAG_03949":null,"SJAG_03954":null,"SJAG_03956":null,"SJAG_03957":null,"SJAG_03982":null,"SJAG_03983":null,"SJAG_03986":null,"SJAG_03987":null,"SJAG_03989":null,"SJAG_03995":null,"SJAG_03997":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04005":null,"SJAG_04008":null,"SJAG_04010":null,"SJAG_04012":null,"SJAG_04014":null,"SJAG_04016":null,"SJAG_04023":null,"SJAG_04030":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04040":null,"SJAG_04044":null,"SJAG_04049":null,"SJAG_04052":null,"SJAG_04059":null,"SJAG_04061":null,"SJAG_04064":null,"SJAG_04066":null,"SJAG_04073":null,"SJAG_04074":null,"SJAG_04076":null,"SJAG_04077":null,"SJAG_04080":null,"SJAG_04093":null,"SJAG_04097":null,"SJAG_04100":null,"SJAG_04108":null,"SJAG_04114":null,"SJAG_04116":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04141":null,"SJAG_04143":null,"SJAG_04146":null,"SJAG_04148":null,"SJAG_04150":null,"SJAG_04163":null,"SJAG_04172":null,"SJAG_04177":null,"SJAG_04180":null,"SJAG_04183":null,"SJAG_04186":null,"SJAG_04190":null,"SJAG_04194":null,"SJAG_04196":null,"SJAG_04197":null,"SJAG_04203":null,"SJAG_04205":null,"SJAG_04208":null,"SJAG_04213":null,"SJAG_04214":null,"SJAG_04221":null,"SJAG_04227":null,"SJAG_04230":null,"SJAG_04232":null,"SJAG_04237":null,"SJAG_04245":null,"SJAG_04253":null,"SJAG_04255":null,"SJAG_04256":null,"SJAG_04257":null,"SJAG_04259":null,"SJAG_04266":null,"SJAG_04271":null,"SJAG_04272":null,"SJAG_04274":null,"SJAG_04275":null,"SJAG_04280":null,"SJAG_04283":null,"SJAG_04287":null,"SJAG_04290":null,"SJAG_04293":null,"SJAG_04294":null,"SJAG_04303":null,"SJAG_04304":null,"SJAG_04312":null,"SJAG_04315":null,"SJAG_04317":null,"SJAG_04319":null,"SJAG_04322":null,"SJAG_04332":null,"SJAG_04338":null,"SJAG_04343":null,"SJAG_04347":null,"SJAG_04348":null,"SJAG_04355":null,"SJAG_04358":null,"SJAG_04369":null,"SJAG_04370":null,"SJAG_04372":null,"SJAG_04375":null,"SJAG_04379":null,"SJAG_04387":null,"SJAG_04389":null,"SJAG_04391":null,"SJAG_04395":null,"SJAG_04396":null,"SJAG_04397":null,"SJAG_04412":null,"SJAG_04413":null,"SJAG_04417":null,"SJAG_04418":null,"SJAG_04428":null,"SJAG_04450":null,"SJAG_04454":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04461":null,"SJAG_04462":null,"SJAG_04464":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04470":null,"SJAG_04479":null,"SJAG_04483":null,"SJAG_04489":null,"SJAG_04492":null,"SJAG_04497":null,"SJAG_04498":null,"SJAG_04502":null,"SJAG_04508":null,"SJAG_04509":null,"SJAG_04513":null,"SJAG_04522":null,"SJAG_04524":null,"SJAG_04528":null,"SJAG_04529":null,"SJAG_04530":null,"SJAG_04531":null,"SJAG_04534":null,"SJAG_04538":null,"SJAG_04547":null,"SJAG_04553":null,"SJAG_04554":null,"SJAG_04558":null,"SJAG_04560":null,"SJAG_04561":null,"SJAG_04566":null,"SJAG_04573":null,"SJAG_04574":null,"SJAG_04576":null,"SJAG_04578":null,"SJAG_04581":null,"SJAG_04586":null,"SJAG_04595":null,"SJAG_04596":null,"SJAG_04597":null,"SJAG_04598":null,"SJAG_04599":null,"SJAG_04602":null,"SJAG_04603":null,"SJAG_04613":null,"SJAG_04615":null,"SJAG_04620":null,"SJAG_04621":null,"SJAG_04623":null,"SJAG_04624":null,"SJAG_04638":null,"SJAG_04639":null,"SJAG_04640":null,"SJAG_04643":null,"SJAG_04644":null,"SJAG_04654":null,"SJAG_04655":null,"SJAG_04661":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04669":null,"SJAG_04670":null,"SJAG_04671":null,"SJAG_04684":null,"SJAG_04690":null,"SJAG_04692":null,"SJAG_04696":null,"SJAG_04699":null,"SJAG_04703":null,"SJAG_04724":null,"SJAG_04732":null,"SJAG_04734":null,"SJAG_04739":null,"SJAG_04744":null,"SJAG_04745":null,"SJAG_04746":null,"SJAG_04748":null,"SJAG_04752":null,"SJAG_04755":null,"SJAG_04758":null,"SJAG_04763":null,"SJAG_04768":null,"SJAG_04776":null,"SJAG_04781":null,"SJAG_04791":null,"SJAG_04793":null,"SJAG_04815":null,"SJAG_04816":null,"SJAG_04822":null,"SJAG_04841":null,"SJAG_04844":null,"SJAG_04853":null,"SJAG_04855":null,"SJAG_04857":null,"SJAG_04862":null,"SJAG_04863":null,"SJAG_04868":null,"SJAG_04879":null,"SJAG_04883":null,"SJAG_04884":null,"SJAG_04886":null,"SJAG_04887":null,"SJAG_04891":null,"SJAG_04898":null,"SJAG_04899":null,"SJAG_04900":null,"SJAG_04901":null,"SJAG_04909":null,"SJAG_04911":null,"SJAG_04918":null,"SJAG_04922":null,"SJAG_04930":null,"SJAG_04936":null,"SJAG_04940":null,"SJAG_04942":null,"SJAG_04943":null,"SJAG_04947":null,"SJAG_04950":null,"SJAG_04960":null,"SJAG_04965":null,"SJAG_04966":null,"SJAG_04968":null,"SJAG_04972":null,"SJAG_04978":null,"SJAG_04981":null,"SJAG_04982":null,"SJAG_04989":null,"SJAG_04991":null,"SJAG_04992":null,"SJAG_04995":null,"SJAG_04996":null,"SJAG_04998":null,"SJAG_04999":null,"SJAG_05000":null,"SJAG_05001":null,"SJAG_05003":null,"SJAG_05009":null,"SJAG_05017":null,"SJAG_05019":null,"SJAG_05020":null,"SJAG_05025":null,"SJAG_05032":null,"SJAG_05105":null,"SJAG_05161":null,"SJAG_05173":null,"SJAG_05179":null,"SJAG_05180":null,"SJAG_05184":null,"SJAG_05185":null,"SJAG_05192":null,"SJAG_05193":null,"SJAG_05194":null,"SJAG_05195":null,"SJAG_05196":null,"SJAG_05199":null,"SJAG_05207":null,"SJAG_05209":null,"SJAG_05220":null,"SJAG_05221":null,"SJAG_05223":null,"SJAG_05226":null,"SJAG_05231":null,"SJAG_05237":null,"SJAG_05240":null,"SJAG_05241":null,"SJAG_05245":null,"SJAG_05248":null,"SJAG_05260":null,"SJAG_05261":null,"SJAG_05265":null,"SJAG_05266":null,"SJAG_05268":null,"SJAG_05273":null,"SJAG_05280":null,"SJAG_05282":null,"SJAG_05285":null,"SJAG_05289":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05296":null,"SJAG_05297":null,"SJAG_05300":null,"SJAG_05302":null,"SJAG_05305":null,"SJAG_05306":null,"SJAG_05309":null,"SJAG_05313":null,"SJAG_05315":null,"SJAG_05319":null,"SJAG_05321":null,"SJAG_05323":null,"SJAG_05329":null,"SJAG_05333":null,"SJAG_05344":null,"SJAG_05345":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_05398":null,"SJAG_05414":null,"SJAG_05679":null,"SJAG_05950":null,"SJAG_05978":null,"SJAG_05979":null,"SJAG_06002":null,"SJAG_06046":null,"SJAG_06135":null,"SJAG_06270":null,"SJAG_06309":null,"SJAG_06392":null,"SJAG_06440":null,"SJAG_06468":null,"SJAG_06514":null,"SJAG_06597":null,"SJAG_06608":null,"SJAG_06641":null,"SJAG_06642":null,"SJAG_07002":null,"SJAG_07005":null,"SJAG_07008":null,"SJAG_07011":null,"SJAG_07018":null,"SJAG_16457":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular component organization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:21802294":null,"PMID:24184107":null,"PMID:26774782":null,"PMID:27059155":null,"PMID:28954740":null,"PMID:32243490":null,"PMID:32915139":null,"PMID:33495454":null,"PMID:35226668":null},"secondary_identifiers":["GO:0044235","GO:0071842"],"synonyms":[{"name":"cell organisation","type":"exact"},{"name":"cell organization and biogenesis","type":"related"},{"name":"cellular component organisation at cellular level","type":"exact"},{"name":"cellular component organisation in other organism","type":"exact"},{"name":"cellular component organization at cellular level","type":"exact"},{"name":"cellular component organization in other organism","type":"exact"}],"termid":"GO:0016043","terms_by_termid":{"GO:0000001":null,"GO:0000002":null,"GO:0000022":null,"GO:0000027":null,"GO:0000028":null,"GO:0000045":null,"GO:0000070":null,"GO:0000073":null,"GO:0000132":null,"GO:0000147":null,"GO:0000183":null,"GO:0000212":null,"GO:0000226":null,"GO:0000244":null,"GO:0000245":null,"GO:0000266":null,"GO:0000280":null,"GO:0000348":null,"GO:0000349":null,"GO:0000350":null,"GO:0000354":null,"GO:0000387":null,"GO:0000388":null,"GO:0000389":null,"GO:0000390":null,"GO:0000393":null,"GO:0000395":null,"GO:0000492":null,"GO:0000493":null,"GO:0000707":null,"GO:0000709":null,"GO:0000712":null,"GO:0000722":null,"GO:0000723":null,"GO:0000730":null,"GO:0000742":null,"GO:0000915":null,"GO:0000917":null,"GO:0000921":null,"GO:0000972":null,"GO:0000973":null,"GO:0001188":null,"GO:0001578":null,"GO:0001731":null,"GO:0001732":null,"GO:0002184":null,"GO:0003400":null,"GO:0006264":null,"GO:0006265":null,"GO:0006294":null,"GO:0006325":null,"GO:0006334":null,"GO:0006335":null,"GO:0006337":null,"GO:0006338":null,"GO:0006376":null,"GO:0006415":null,"GO:0006449":null,"GO:0006617":null,"GO:0006625":null,"GO:0006884":null,"GO:0006900":null,"GO:0006901":null,"GO:0006906":null,"GO:0006998":null,"GO:0006999":null,"GO:0007004":null,"GO:0007005":null,"GO:0007006":null,"GO:0007007":null,"GO:0007008":null,"GO:0007009":null,"GO:0007015":null,"GO:0007019":null,"GO:0007020":null,"GO:0007021":null,"GO:0007029":null,"GO:0007030":null,"GO:0007031":null,"GO:0007032":null,"GO:0007033":null,"GO:0007052":null,"GO:0007063":null,"GO:0007064":null,"GO:0007076":null,"GO:0007077":null,"GO:0007079":null,"GO:0007084":null,"GO:0007088":null,"GO:0007091":null,"GO:0007094":null,"GO:0007127":null,"GO:0007129":null,"GO:0007131":null,"GO:0007135":null,"GO:0008053":null,"GO:0008361":null,"GO:0009992":null,"GO:0010032":null,"GO:0010257":null,"GO:0010265":null,"GO:0010637":null,"GO:0010772":null,"GO:0010774":null,"GO:0010780":null,"GO:0010789":null,"GO:0010821":null,"GO:0010833":null,"GO:0010845":null,"GO:0010846":null,"GO:0010964":null,"GO:0016226":null,"GO:0016233":null,"GO:0016240":null,"GO:0016320":null,"GO:0016558":null,"GO:0016559":null,"GO:0016560":null,"GO:0016562":null,"GO:0017004":null,"GO:0017121":null,"GO:0022618":null,"GO:0030036":null,"GO:0030041":null,"GO:0030042":null,"GO:0030100":null,"GO:0030307":null,"GO:0030466":null,"GO:0030476":null,"GO:0030833":null,"GO:0030866":null,"GO:0030950":null,"GO:0030951":null,"GO:0030952":null,"GO:0030953":null,"GO:0030954":null,"GO:0030989":null,"GO:0030994":null,"GO:0030999":null,"GO:0031023":null,"GO:0031024":null,"GO:0031025":null,"GO:0031030":null,"GO:0031031":null,"GO:0031032":null,"GO:0031048":null,"GO:0031106":null,"GO:0031110":null,"GO:0031117":null,"GO:0031122":null,"GO:0031134":null,"GO:0031321":null,"GO:0031322":null,"GO:0031445":null,"GO:0031453":null,"GO:0031468":null,"GO:0031505":null,"GO:0031507":null,"GO:0031508":null,"GO:0031509":null,"GO:0031582":null,"GO:0031619":null,"GO:0031671":null,"GO:0031848":null,"GO:0032042":null,"GO:0032043":null,"GO:0032118":null,"GO:0032120":null,"GO:0032121":null,"GO:0032185":null,"GO:0032210":null,"GO:0032215":null,"GO:0032220":null,"GO:0032231":null,"GO:0032790":null,"GO:0032889":null,"GO:0032955":null,"GO:0032956":null,"GO:0032979":null,"GO:0033316":null,"GO:0033615":null,"GO:0033617":null,"GO:0033696":null,"GO:0033962":null,"GO:0034058":null,"GO:0034063":null,"GO:0034080":null,"GO:0034085":null,"GO:0034087":null,"GO:0034203":null,"GO:0034314":null,"GO:0034316":null,"GO:0034462":null,"GO:0034496":null,"GO:0034551":null,"GO:0034553":null,"GO:0034728":null,"GO:0035493":null,"GO:0035494":null,"GO:0035694":null,"GO:0040020":null,"GO:0040029":null,"GO:0042144":null,"GO:0042255":null,"GO:0042256":null,"GO:0042407":null,"GO:0043007":null,"GO:0043248":null,"GO:0043504":null,"GO:0043570":null,"GO:0043622":null,"GO:0044396":null,"GO:0044571":null,"GO:0044572":null,"GO:0044821":null,"GO:0044837":null,"GO:0045010":null,"GO:0045033":null,"GO:0045039":null,"GO:0045040":null,"GO:0045046":null,"GO:0045048":null,"GO:0045128":null,"GO:0045141":null,"GO:0045143":null,"GO:0045144":null,"GO:0045332":null,"GO:0045458":null,"GO:0045793":null,"GO:0045806":null,"GO:0045807":null,"GO:0045814":null,"GO:0045815":null,"GO:0045842":null,"GO:0045875":null,"GO:0045876":null,"GO:0045899":null,"GO:0045905":null,"GO:0046785":null,"GO:0048194":null,"GO:0048205":null,"GO:0048210":null,"GO:0048268":null,"GO:0048280":null,"GO:0048284":null,"GO:0048288":null,"GO:0051013":null,"GO:0051016":null,"GO:0051017":null,"GO:0051123":null,"GO:0051131":null,"GO:0051177":null,"GO:0051225":null,"GO:0051228":null,"GO:0051232":null,"GO:0051256":null,"GO:0051292":null,"GO:0051300":null,"GO:0051306":null,"GO:0051307":null,"GO:0051315":null,"GO:0051382":null,"GO:0051383":null,"GO:0051415":null,"GO:0051417":null,"GO:0051455":null,"GO:0051456":null,"GO:0051516":null,"GO:0051517":null,"GO:0051519":null,"GO:0051523":null,"GO:0051598":null,"GO:0051639":null,"GO:0051685":null,"GO:0051754":null,"GO:0051755":null,"GO:0051764":null,"GO:0060172":null,"GO:0060236":null,"GO:0060237":null,"GO:0060906":null,"GO:0061024":null,"GO:0061025":null,"GO:0061188":null,"GO:0061191":null,"GO:0061192":null,"GO:0061387":null,"GO:0061572":null,"GO:0061573":null,"GO:0061753":null,"GO:0061796":null,"GO:0061804":null,"GO:0061805":null,"GO:0061817":null,"GO:0062123":null,"GO:0062195":null,"GO:0062209":null,"GO:0070072":null,"GO:0070096":null,"GO:0070126":null,"GO:0070196":null,"GO:0070197":null,"GO:0070462":null,"GO:0070507":null,"GO:0070583":null,"GO:0070649":null,"GO:0070682":null,"GO:0070828":null,"GO:0070898":null,"GO:0070941":null,"GO:0071520":null,"GO:0071562":null,"GO:0071763":null,"GO:0071765":null,"GO:0071788":null,"GO:0071816":null,"GO:0071962":null,"GO:0072318":null,"GO:0072344":null,"GO:0090006":null,"GO:0090052":null,"GO:0090053":null,"GO:0090055":null,"GO:0090110":null,"GO:0090114":null,"GO:0090135":null,"GO:0090139":null,"GO:0090141":null,"GO:0090149":null,"GO:0090158":null,"GO:0090258":null,"GO:0090267":null,"GO:0090297":null,"GO:0090306":null,"GO:0090307":null,"GO:0090522":null,"GO:0097036":null,"GO:0097250":null,"GO:0097320":null,"GO:0097352":null,"GO:0097576":null,"GO:0097753":null,"GO:0099022":null,"GO:0099050":null,"GO:0099606":null,"GO:0099607":null,"GO:0101024":null,"GO:0101026":null,"GO:0110009":null,"GO:0110161":null,"GO:0110162":null,"GO:0120009":null,"GO:0120010":null,"GO:0120011":null,"GO:0120306":null,"GO:0140013":null,"GO:0140042":null,"GO:0140278":null,"GO:0140281":null,"GO:0140331":null,"GO:0140429":null,"GO:0140454":null,"GO:0140456":null,"GO:0140462":null,"GO:0140499":null,"GO:0140515":null,"GO:0140516":null,"GO:0140529":null,"GO:0140530":null,"GO:0140572":null,"GO:0140588":null,"GO:0140641":null,"GO:0140642":null,"GO:0140673":null,"GO:0140708":null,"GO:0140718":null,"GO:0140719":null,"GO:0140727":null,"GO:0140861":null,"GO:0140898":null,"GO:0141005":null,"GO:0141194":null,"GO:0180023":null,"GO:1901098":null,"GO:1901673":null,"GO:1902103":null,"GO:1902404":null,"GO:1902424":null,"GO:1902425":null,"GO:1902426":null,"GO:1902441":null,"GO:1902626":null,"GO:1902681":null,"GO:1902775":null,"GO:1902794":null,"GO:1902795":null,"GO:1902801":null,"GO:1902846":null,"GO:1902917":null,"GO:1902977":null,"GO:1902985":null,"GO:1903023":null,"GO:1903024":null,"GO:1903087":null,"GO:1903241":null,"GO:1903259":null,"GO:1903359":null,"GO:1903373":null,"GO:1903380":null,"GO:1903473":null,"GO:1903475":null,"GO:1903479":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:1904541":null,"GO:1904595":null,"GO:1904600":null,"GO:1904802":null,"GO:1904868":null,"GO:1904967":null,"GO:1905047":null,"GO:1905143":null,"GO:1905191":null,"GO:1905263":null,"GO:1905318":null,"GO:1905323":null,"GO:1905324":null,"GO:1905325":null,"GO:1905326":null,"GO:1905557":null,"GO:1905560":null,"GO:1905561":null,"GO:1905757":null,"GO:1905758":null,"GO:1990113":null,"GO:1990114":null,"GO:1990115":null,"GO:1990344":null,"GO:1990395":null,"GO:1990456":null,"GO:1990571":null,"GO:1990627":null,"GO:1990734":null,"GO:1990758":null,"GO:1990809":null,"GO:1990810":null,"GO:1990813":null,"GO:1990854":null,"GO:1990893":null,"GO:1990918":null,"GO:1990942":null,"GO:1990949":null,"GO:1990950":null,"GO:2000369":null,"GO:2000432":null,"GO:2000786":null,"GO:2000816":null,"GO:2001178":null}}


