# terms

id: MONDO:0004273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign and well circumscribed neoplasm that arises from the breast. It is characterized by the proliferation of epithelial cells with extensive apocrine metaplasia.","definition_xrefs":["NCIT:C40383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast adenoma","termid":"MONDO:0002058"},{"relation_name":"is_a","term_name":"apocrine adenoma","termid":"MONDO:0002804"},{"relation_name":"is_a","term_name":"sweat gland adenoma","termid":"MONDO:0021110"},{"relation_name":"is_a","term_name":"benign neoplasm of sweat gland","termid":"MONDO:0021489"},{"relation_name":"is_a","term_name":"benign epithelial skin neoplasm","termid":"MONDO:0024666"}],"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":"breast apocrine adenoma","secondary_identifiers":["icd11.foundation:636674012","DOID:7540","MEDGEN:235590","UMLS:C1388299"],"synonyms":[{"name":"apocrine adenoma of breast","type":"exact"},{"name":"breast apocrine adenoma","type":"exact"}],"termid":"MONDO:0004273","xrefs":{"Monarch":{"xref_id":"0004273"}}}


id: MONDO:0019360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spotted fever","termid":"MONDO:0001195"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rickettsialpox","secondary_identifiers":["ICD9:083.2","MESH:D012288","MEDGEN:19803","Orphanet:83312","UMLS:C0035597","MedDRA:10039137","SCTID:75096007","ICD10CM:A79.1","icd11.foundation:1005140361","GARD:19030","DOID:11103"],"synonyms":[{"name":"Rickettsia akari spotted fever","type":"exact"},{"name":"vesicular rickettsiosis","type":"exact"}],"termid":"MONDO:0019360","xrefs":{"Monarch":{"xref_id":"0019360"}}}


id: MONDO:0016385
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by the association of hypogonadism due to primary gonadal failure, mitral valve prolapse, mild intellectual deficit and short stature.","definition_xrefs":["Orphanet:2233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadism-mitral valve prolapse-intellectual disability syndrome","secondary_identifiers":["UMLS:C2931685","MEDGEN:444117","MESH:C537981","SCTID:721841001","GARD:1078"],"synonyms":[{"name":"Cantalamessa Baldini Ambrosi syndrome","type":"related"},{"name":"Cantalamessa-Baldini-Ambrosi syndrome","type":"exact"},{"name":"primary gonadal failure, short stature, mitral valve prolapse, and intellectual disability","type":"related"},{"name":"primary gonadal failure, short stature, mitral valve prolapse, and mental retardation","type":"related"}],"termid":"MONDO:0016385","xrefs":{"Monarch":{"xref_id":"0016385"}}}


id: GO:0070676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The invagination of the endosome membrane and resulting formation of a vesicle within the lumen of the endosome.","definition_xrefs":["PMID:19234443","GOC:jp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle budding from membrane","termid":"GO:0006900"},{"relation_name":"is_a","term_name":"endosome organization","termid":"GO:0007032"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192","GO:0061024"],"is_obsolete":false,"name":"intralumenal vesicle formation","synonyms":[{"name":"endosome membrane budding","type":"exact"}],"termid":"GO:0070676"}


id: GO:1903187
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of vitellogenesis.","definition_xrefs":["GO_REF:0000058","PMID:19467235","GOC:TermGenie","GOC:mr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of vitellogenesis","termid":"GO:1903186"},{"relation_name":"negatively_regulates","term_name":"vitellogenesis","termid":"GO:0007296"}],"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 vitellogenesis","synonyms":[{"name":"down regulation of vitellogenesis","type":"exact"},{"name":"down regulation of yolk production","type":"exact"},{"name":"down-regulation of vitellogenesis","type":"exact"},{"name":"down-regulation of yolk production","type":"exact"},{"name":"downregulation of vitellogenesis","type":"exact"},{"name":"downregulation of yolk production","type":"exact"},{"name":"inhibition of vitellogenesis","type":"narrow"},{"name":"inhibition of yolk production","type":"narrow"},{"name":"negative regulation of yolk production","type":"exact"}],"termid":"GO:1903187"}


id: MONDO:0851103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A female reproductive system disease that is located in Bartholin's gland.","definition_xrefs":["DOID:60002"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bartholin's gland disease","secondary_identifiers":["UMLS:C0477776","MEDGEN:635229"],"termid":"MONDO:0851103","xrefs":{"Monarch":{"xref_id":"0851103"}}}


id: PBO:0058123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4425","termid":"PBO:0058123"}


id: PBO:0069323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 581, pseudogene","termid":"PBO:0069323"}


id: GO:0006201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of guanosine monophosphate into other compounds, including inosine monophosphate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GMP catabolic process","termid":"GO:0046038"},{"relation_name":"is_a","term_name":"IMP metabolic process","termid":"GO:0046040"}],"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:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"GMP catabolic process to IMP","synonyms":[{"name":"GMP breakdown to IMP","type":"exact"},{"name":"GMP degradation to IMP","type":"exact"}],"termid":"GO:0006201"}


id: GO:0140572
data:
  {"annotated_genes":["SJAG_02848"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104723],"is_not":false,"summary":null,"term":"GO:0140572"}]},"cv_name":"biological_process","definition":"The division of a vacuole within a cell to form two or more separate vacuoles.","definition_xrefs":["PMID:19643199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle fission","termid":"GO:0048285"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02848":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"vacuole fission","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140572","terms_by_termid":{"GO:0140572":null}}


id: MONDO:0016180
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hematological disease associated with an acquired peripheral neuropathy (obsolete MONDO:0016180)","secondary_identifiers":["Orphanet:209016"],"termid":"MONDO:0016180","xrefs":{"Monarch":{"xref_id":"0016180"}}}


id: GO:0030010
data:
  {"annotated_genes":["SJAG_04724","SJAG_04509","SJAG_01901","SJAG_00216","SJAG_03596","SJAG_03453","SJAG_03754","SJAG_03705","SJAG_02651","SJAG_02838","SJAG_02695","SJAG_00594","SJAG_04322","SJAG_04624","SJAG_03486","SJAG_00845","SJAG_00317","SJAG_01794","SJAG_00514","SJAG_00030","SJAG_04522","SJAG_01373","SJAG_01456","SJAG_03126","SJAG_02536","SJAG_03625","SJAG_00140","SJAG_03581","SJAG_04653","SJAG_02737"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72628,80243,82034,92790,94217,95422,99145,116796],"is_not":false,"summary":null,"term":"GO:0030010"},{"annotations":[118479,119905,108824,101693,105440,90000,112751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051523"},{"annotations":[94537,106610,121415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061171"},{"annotations":[118947,106502,98924,106833,78222],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000132"},{"annotations":[92907],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1904846"},{"annotations":[114468,109584,105651],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0061173"},{"annotations":[118585,109585],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2000784"},{"annotations":[96532,70967],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000114"}]},"cv_name":"biological_process","definition":"The specification and formation of anisotropic intracellular organization or cell growth patterns.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment or maintenance of cell polarity","termid":"GO:0007163"}],"gene_count":30,"genes_by_uniquename":{"SJAG_00030":null,"SJAG_00140":null,"SJAG_00216":null,"SJAG_00317":null,"SJAG_00514":null,"SJAG_00594":null,"SJAG_00845":null,"SJAG_01373":null,"SJAG_01456":null,"SJAG_01794":null,"SJAG_01901":null,"SJAG_02536":null,"SJAG_02651":null,"SJAG_02695":null,"SJAG_02737":null,"SJAG_02838":null,"SJAG_03126":null,"SJAG_03453":null,"SJAG_03486":null,"SJAG_03581":null,"SJAG_03596":null,"SJAG_03625":null,"SJAG_03705":null,"SJAG_03754":null,"SJAG_04322":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04624":null,"SJAG_04653":null,"SJAG_04724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"establishment of cell polarity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:30664646":null},"secondary_identifiers":["GO:0000283","GO:0030468"],"synonyms":[{"name":"bud site selection/establishment of cell polarity","type":"narrow"},{"name":"cell polarization","type":"exact"}],"termid":"GO:0030010","terms_by_termid":{"GO:0000132":null,"GO:0030010":null,"GO:0051523":null,"GO:0061171":null,"GO:0061173":null,"GO:1904846":null,"GO:2000114":null,"GO:2000784":null}}


id: GO:0045965
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways involving ecdysteroids.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ecdysteroid metabolic process","termid":"GO:0007553"},{"relation_name":"is_a","term_name":"negative regulation of hormone metabolic process","termid":"GO:0032351"},{"relation_name":"is_a","term_name":"negative regulation of steroid metabolic process","termid":"GO:0045939"},{"relation_name":"negatively_regulates","term_name":"ecdysteroid metabolic process","termid":"GO:0045455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of ecdysteroid metabolic process","synonyms":[{"name":"down regulation of ecdysteroid metabolic process","type":"exact"},{"name":"down-regulation of ecdysteroid metabolic process","type":"exact"},{"name":"downregulation of ecdysteroid metabolic process","type":"exact"},{"name":"inhibition of ecdysteroid metabolic process","type":"narrow"},{"name":"negative regulation of ecdysteroid metabolism","type":"exact"}],"termid":"GO:0045965"}


id: GO:0044595
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: S-adenosyl-L-methionine + 3-decaprenyl-4,5-dihydroxybenzoate = S-adenosyl-L-homocysteine + 3-decaprenyl-4-hydroxy-5-methoxybenzoate.","definition_xrefs":["PMID:10777520"],"gene_count":0,"genotype_count":0,"name":"obsolete decaprenyldihydroxybenzoate methyltransferase activity (obsolete GO:0044595)","termid":"GO:0044595"}


id: PBO:0054914
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 2328","termid":"PBO:0054914"}


id: PBO:0089841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3, unknown biological role, implicated in protein catabolic process","termid":"PBO:0089841"}


id: MONDO:1011953
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal dysplasia, non-human animal","secondary_identifiers":["OMIA:000937"],"termid":"MONDO:1011953","xrefs":{"Monarch":{"xref_id":"1011953"}}}


id: PBO:0034266
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_iterative_homology_relationship_with","termid":"PBO:0034266"}


id: SO:0000963
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Structural unit composed of a self-replicating, single-stranded, linear RNA molecule.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"linear","termid":"SO:0000987"},{"relation_name":"is_a","term_name":"single_stranded_RNA_chromosome","termid":"SO:0000962"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"linear_single_stranded_RNA_chromosome","synonyms":[{"name":"linear single stranded RNA chromosome","type":"exact"}],"termid":"SO:0000963"}


id: PR:O59726
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fnx2 gene.","definition_xrefs":["UniProtKB:O59726","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":"vacuolar membrane amino acid uptake transporter fnx2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3E7.06c","synonyms":[{"name":"Spom972h-fnx2","type":"exact"}],"termid":"PR:O59726"}


id: PBO:0111798
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G-patch domain","termid":"PBO:0111798"}


id: GO:1905441
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 chondroitin 4'-sulfate stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:22365850"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"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 chondroitin 4'-sulfate","termid":"GO:1905441"}


id: MONDO:0004414
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A spectrum of endometrial abnormalities that occur in women who use tamoxifen to treat or prevent the development of breast cancer. These abnormalities include endometrial polyps, endometrial hyperplasia, and endometrial carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrial disorder","termid":"MONDO:0000931"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tamoxifen-related endometrial lesion","secondary_identifiers":["NCIT:C40159","MEDGEN:271571","DOID:7962","UMLS:C1515212"],"synonyms":[{"name":"tamoxifen-related endometrial disorder","type":"exact"}],"termid":"MONDO:0004414","xrefs":{"Monarch":{"xref_id":"0004414"}}}


id: MONDO:0007764
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sclerozing bone disorder characterized by generalized skeletal densification, particularly of the cranial vault and tubular long bones, which is not associated to an increased risk of fracture.","definition_xrefs":["Orphanet:2790"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with increased bone density (obsolete MONDO:0019703)","termid":"MONDO:0019703"},{"relation_name":"is_a","term_name":"hyperostosis","termid":"MONDO:0002185"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal dominant osteosclerosis, Worth type","secondary_identifiers":["OMIM:607636","UMLS:C0432273","DOID:0080037","MEDGEN:140932","GARD:390","OMIM:144750","SCTID:254131007","icd11.foundation:1038854228"],"synonyms":[{"name":"Ostéosclérose autosomique dominante type Worth","type":"exact"},{"name":"VBCH2","type":"related"},{"name":"Van Buchem disease type 2","type":"related"},{"name":"Van Buchem disease, type 2","type":"related"},{"name":"Worth syndrome","type":"exact"},{"name":"Worth's syndrome","type":"exact"},{"name":"autosomal dominant endosteal hyperostosis","type":"exact"},{"name":"autosomal dominant osteosclerosis","type":"exact"},{"name":"benign form of Worth hyperostosis corticalis generalisata with torus platinus","type":"exact"},{"name":"endosteal hyperostosis, Worth type","type":"exact"},{"name":"endosteal hyperostosis, autosomal dominant","type":"related"},{"name":"hyperostosis corticalis generalisata, benign form of Worth with torus palatinus","type":"related"},{"name":"hyperostosis corticalis generalisata, benign form of Worth, with torus palatinus","type":"related"},{"name":"hyperostosis, endosteal","type":"exact"},{"name":"osteosclerosis of the skull and enlarged mandible","type":"related"},{"name":"osteosclerosis, autosomal dominant","type":"related"},{"name":"osteosclerosis, autosomal dominant, Worth type","type":"related"}],"termid":"MONDO:0007764","xrefs":{"Monarch":{"xref_id":"0007764"}}}


id: PBO:0002303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing associated factor Saf2","termid":"PBO:0002303"}


id: MONDO:0013013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"auriculocondylar syndrome","termid":"MONDO:0000107"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"question mark ears, isolated","secondary_identifiers":["OMIM:612798","GARD:15583","UMLS:C2748545","MEDGEN:411238"],"synonyms":[{"name":"Cosman deformity of the auricle","type":"related"},{"name":"QME","type":"related"},{"name":"auricular cleft, congenital","type":"related"},{"name":"ears, prominent and constricted","type":"related"},{"name":"question MARK ears, isolated","type":"related"},{"name":"question mark ears, isolated","type":"exact"}],"termid":"MONDO:0013013","xrefs":{"Monarch":{"xref_id":"0013013"}}}


id: PBO:0114214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-lactate dehydrogenase Ldh1","termid":"PBO:0114214"}


id: GO:0044451
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any constituent part of the nucleoplasm, that part of the nuclear content other than the chromosomes or the nucleolus.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleoplasm part (obsolete GO:0044451)","termid":"GO:0044451"}


id: PBO:0089508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cornichon family protein Erv14","termid":"PBO:0089508"}


id: MONDO:0007370
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":"coracoclavicular joint, anomalous","secondary_identifiers":["OMIM:121350","UMLS:C1852561","MESH:C565161","MEDGEN:377706"],"synonyms":[{"name":"coracoclavicular joint, anomalous","type":"exact"}],"termid":"MONDO:0007370","xrefs":{"Monarch":{"xref_id":"0007370"}}}


id: PBO:0081926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 968, pseudogene","termid":"PBO:0081926"}


id: FYPO:0007091
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 negative regulation of transcription by zinc occurs to a greater extent than normal. Specific genes that are normally not transcribed in the presence of zinc ions are not derepressed in the mutant under conditions that derepress transcription in wild type cells.","definition_xrefs":["PMID:31515876","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal negative regulation of transcription during vegetative growth","termid":"FYPO:0000624"},{"relation_name":"is_a","term_name":"abnormal regulation of transcription by nutrient","termid":"FYPO:0007090"}],"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:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0006551","FYPO:0000298","FYPO:0000002"],"is_obsolete":false,"name":"increased negative regulation of transcription by zinc","synonyms":[{"name":"increased gene repression in response to zinc","type":"exact"},{"name":"increased negative regulation of transcription by zinc during mitotic cell cycle","type":"related"},{"name":"increased negative regulation of transcription by zinc during vegetative growth","type":"exact"},{"name":"increased negative regulation of transcription in response to zinc","type":"exact"}],"termid":"FYPO:0007091"}


id: GO:0160038
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a somatic sensory system over time from its formation to the mature structure. Somatic sensory system is the sensory system for the sense of touch and pain.","definition_xrefs":["PMID:31399790","PMID:25832476"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory system development","termid":"GO:0048880"}],"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":"somatic sensory system development","synonyms":[{"name":"somatosensory system development","type":"exact"}],"termid":"GO:0160038"}


id: PBO:0005673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uricase (predicted)","termid":"PBO:0005673"}


id: MONDO:0032889
data:
  {"annotated_genes":["SJAG_03931","SJAG_00142"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88741,88742],"is_not":false,"summary":null,"term":"MONDO:0032889"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00142":null,"SJAG_03931":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"Poirier-Bienvenu neurodevelopmental syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618732","Orphanet:689397","UMLS:C5231482","MEDGEN:1684718"],"synonyms":[{"name":"POBINDS","type":"related"},{"name":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME","type":"related"}],"termid":"MONDO:0032889","terms_by_termid":{"MONDO:0032889":null},"xrefs":{"Monarch":{"xref_id":"0032889"}}}


id: PBO:0051099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 1-2","termid":"PBO:0051099"}


id: GO:0043776
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosylmethionine + cobalt-precorrin 6B = S-adenosylhomocysteine + cobalt-precorrin 7.","definition_xrefs":["MetaCyc:RXN-8766"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"cobalt-precorrin-6B C5-methyltransferase activity","secondary_identifiers":["RHEA:36067"],"synonyms":[{"name":"cobalt-precorrin 6B C5-methyltransferase activity","type":"exact"},{"name":"precorrin-6 methyltransferase activity","type":"exact"},{"name":"precorrin-6Y C5,15-methyltransferase (decarboxylating)","type":"broad"},{"name":"precorrin-6Y methylase","type":"broad"}],"termid":"GO:0043776"}


id: MONDO:0009834
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pancreatic insufficiency, combined exocrine (obsolete MONDO:0009834)","termid":"MONDO:0009834","xrefs":{"Monarch":{"xref_id":"0009834"}}}


id: GO:1900961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of 17-methylnonadec-1-ene metabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of olefin metabolic process","termid":"GO:1900910"},{"relation_name":"is_a","term_name":"regulation of 17-methylnonadec-1-ene metabolic process","termid":"GO:1900959"},{"relation_name":"positively_regulates","term_name":"17-methylnonadec-1-ene metabolic process","termid":"GO:1900882"}],"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":"positive regulation of 17-methylnonadec-1-ene metabolic process","synonyms":[{"name":"activation of 17-methylnonadec-1-ene metabolic process","type":"narrow"},{"name":"activation of 17-methylnonadec-1-ene metabolism","type":"exact"},{"name":"positive regulation of 17-methylnonadec-1-ene metabolism","type":"exact"},{"name":"up regulation of 17-methylnonadec-1-ene metabolic process","type":"exact"},{"name":"up regulation of 17-methylnonadec-1-ene metabolism","type":"exact"},{"name":"up-regulation of 17-methylnonadec-1-ene metabolic process","type":"exact"},{"name":"up-regulation of 17-methylnonadec-1-ene metabolism","type":"exact"},{"name":"upregulation of 17-methylnonadec-1-ene metabolic process","type":"exact"},{"name":"upregulation of 17-methylnonadec-1-ene metabolism","type":"exact"}],"termid":"GO:1900961"}


id: PBO:0077257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMED7-TICAM2 readthrough","termid":"PBO:0077257"}


id: MOD:01039
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:00036. Remap to MOD:00036.","definition_xrefs":["PubMed:18688235"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01039 hydroxy aspartyl (obsolete MOD:01039)","termid":"MOD:01039"}


id: GO:0106264
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: GTP + L-seryl-[protein] = GDP + H+ + O-phospho-L-seryl-[protein].","definition_xrefs":["RHEA:64020","GOC:sp","PMID:32322062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase activity","termid":"GO:0004672"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0016740","GO:0003824","GO:0140096","GO:0004672"],"is_obsolete":false,"name":"protein serine kinase activity (using GTP as donor)","termid":"GO:0106264"}


id: GO:0062047
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-pipecolic acid + NAD(P)H + O2 + H+ = N-hydroxypipecolic acid + NAD(P)+ + H2O.","definition_xrefs":["PMID:27758894","PMID:28330936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"pipecolic acid N-hydroxylase","termid":"GO:0062047"}


id: MONDO:0971033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A thyroid gland carcinoma composed of groups of carcinoma cells with thymic epithelial differentiation.","definition_xrefs":["DOID:0081457"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid gland carcinoma","termid":"MONDO:0015075"}],"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":"intrathyroid thymic carcinoma","secondary_identifiers":["UMLS:C1704613","MEDGEN:316474"],"termid":"MONDO:0971033","xrefs":{"Monarch":{"xref_id":"0971033"}}}


id: PBO:0082692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the histone deacetylase Rpd3L complex; possibly involved in cell fusion and invasive growth; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082692"}


id: GO:0007417
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the central nervous system over time, from its formation to the mature structure. The central nervous system is the core nervous system that serves an integrating and coordinating function. In vertebrates it consists of the brain and spinal cord. In those invertebrates with a central nervous system it typically consists of a brain, cerebral ganglia and a nerve cord.","definition_xrefs":["ISBN:0582227089","GOC:jid","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"system development","termid":"GO:0048731"},{"relation_name":"part_of","term_name":"nervous system development","termid":"GO:0007399"}],"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":"central nervous system development","secondary_identifiers":["Wikipedia:Neural_development"],"synonyms":[{"name":"CNS development","type":"exact"}],"termid":"GO:0007417"}


id: PBO:0068546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 152, pseudogene","termid":"PBO:0068546"}


id: GO:0002452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of replacing receptors on B cells, in which RAG gene expression allows continued light-chain gene rearrangement and expression of a new light change which combines with the previous heavy chain to form a new receptor.","definition_xrefs":["GOC:jal","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic recombination of immunoglobulin gene segments","termid":"GO:0016447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0006310","GO:0010467"],"is_obsolete":false,"name":"B cell receptor editing","synonyms":[{"name":"B lymphocyte receptor editing","type":"exact"},{"name":"B-cell receptor editing","type":"exact"},{"name":"B-lymphocyte receptor editing","type":"exact"}],"termid":"GO:0002452"}


id: PBO:0070758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10 pseudogene 14","termid":"PBO:0070758"}


id: GO:0032662
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-19 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-19 production","termid":"GO:0032622"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of interleukin-19 production","secondary_identifiers":["GO:0045384"],"synonyms":[{"name":"regulation of IL-19 production","type":"exact"},{"name":"regulation of interleukin-19 biosynthetic process","type":"narrow"}],"termid":"GO:0032662"}


id: GO:0110054
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of actin filament annealing, i.e. the end-to-end joining of existing actin filaments.","definition_xrefs":["PMID:11575927","PMID:19244341","PMID:15743909","PMID:10585915","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament organization","termid":"GO:0110053"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"regulates","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0030036"],"is_obsolete":false,"name":"regulation of actin filament annealing","termid":"GO:0110054"}


id: PBO:0068319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 19B","termid":"PBO:0068319"}


id: GO:0005176
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a protein-tyrosine kinase receptor Neu/ErbB-2/HER2.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"ErbB-2 class receptor binding","synonyms":[{"name":"ErbB-2 class receptor ligand","type":"narrow"},{"name":"HER2 receptor binding","type":"exact"},{"name":"HER2 receptor ligand","type":"narrow"},{"name":"Neu receptor binding","type":"exact"},{"name":"Neu receptor ligand","type":"narrow"}],"termid":"GO:0005176"}


id: MONDO:0018616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Central serous chorioretinopathy is a disease that causes fluid to build up under the retina, the back part of the inner eye that sends sight information to the brain. The fluid leaks from thechoroid (theblood vessel layer under the retina). The cause of this condition is unknown but stress can be a risk factor. Signs and symptoms include dim and blurred blind spot in the center of vision, distortion of straight linesand seeingobjectsas smaller or farther away. Many cases of central serous chorioretinopathy improve without treatment after 1-2 months. Laser treatment may be an option for other individuals.","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"}],"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 serous chorioretinopathy","secondary_identifiers":["ICD9:362.41","GARD:200","MESH:D056833","Orphanet:443079","SCTID:312956001","MEDGEN:147591","UMLS:C0730328","ICD10CM:H35.71","icd11.foundation:1623925689","NCIT:C115124"],"synonyms":[{"name":"CSC","type":"exact"},{"name":"CSCR","type":"exact"},{"name":"central serous chorioretinopathy after bone marrow transplantation","type":"related"},{"name":"central serous choroidopathy","type":"related"},{"name":"central serous retinopathy","type":"exact"}],"termid":"MONDO:0018616","xrefs":{"Monarch":{"xref_id":"0018616"}}}


id: MONDO:0001186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by persistent or recurrent episodes of feeling detached from one's self (either one's body or one's mental processes), although the sufferer remains aware that this is only a feeling and does not represent reality.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dissociative disorder","termid":"MONDO:0001160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"depersonalization disorder","secondary_identifiers":["ICD9:300.6","DOID:11038","NCIT:C94331","MEDGEN:151919","SCTID:70764005","UMLS:C0683416"],"synonyms":[{"name":"neurotic derealization","type":"exact"}],"termid":"MONDO:0001186","xrefs":{"Monarch":{"xref_id":"0001186"}}}


id: MONDO:0002854
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant soft tissue neoplasm that arises from the prostate gland. Representative examples include leiomyosarcoma, rhabdomyosarcoma, and stromal sarcoma.","definition_xrefs":["NCIT:C7731"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostate cancer","termid":"MONDO:0008315"},{"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":"prostate sarcoma","secondary_identifiers":["UMLS:C0238393","MEDGEN:116060","DOID:4054"],"synonyms":[{"name":"prostate gland sarcoma","type":"exact"},{"name":"prostate sarcoma","type":"exact"},{"name":"sarcoma of prostate","type":"exact"},{"name":"sarcoma of prostate gland","type":"exact"},{"name":"sarcoma of the prostate","type":"exact"}],"termid":"MONDO:0002854","xrefs":{"Monarch":{"xref_id":"0002854"}}}


id: PBO:0045543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrouridine synthase 3 like","termid":"PBO:0045543"}


id: GO:1901910
data:
  {"annotated_genes":["SJAG_04870"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901911"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving adenosine 5'-(hexahydrogen pentaphosphate).","definition_xrefs":["PMID:10090752","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04870":null},"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:0008150","GO:0044281"],"is_obsolete":false,"name":"adenosine 5'-(hexahydrogen pentaphosphate) metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"adenosine 5'-(hexahydrogen pentaphosphate) metabolism","type":"exact"}],"termid":"GO:1901910","terms_by_termid":{"GO:1901911":null}}


id: GO:0002573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized myeloid precursor cell acquires the specialized features of any cell of the myeloid leukocyte lineage.","definition_xrefs":["GOC:add","PMID:16551251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte differentiation","termid":"GO:0002521"},{"relation_name":"is_a","term_name":"myeloid cell differentiation","termid":"GO:0030099"}],"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":"myeloid leukocyte differentiation","synonyms":[{"name":"myeloid leucocyte differentiation","type":"exact"}],"termid":"GO:0002573"}


id: SO:0000660
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000660 DNA_invertase_target_sequence (obsolete SO:0000660)","termid":"SO:0000660"}


id: PBO:0091495
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does not functionally complement S. cerevisiae HAL3","termid":"PBO:0091495"}


id: GO:0070368
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the rate or extent of hepatocyte differentiation.","definition_xrefs":["GOC:mah","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of epithelial cell differentiation","termid":"GO:0030858"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of hepatocyte differentiation","termid":"GO:0070366"},{"relation_name":"positively_regulates","term_name":"hepatocyte differentiation","termid":"GO:0070365"}],"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":"positive regulation of hepatocyte differentiation","synonyms":[{"name":"activation of hepatocyte differentiation","type":"narrow"},{"name":"positive regulation of liver cell differentiation","type":"exact"},{"name":"stimulation of hepatocyte differentiation","type":"narrow"},{"name":"up regulation of hepatocyte differentiation","type":"exact"},{"name":"up-regulation of hepatocyte differentiation","type":"exact"},{"name":"upregulation of hepatocyte differentiation","type":"exact"}],"termid":"GO:0070368"}


id: FYPO:0006857
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which methylation of lysine at position 37 of histone H3 is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K37 methylation","termid":"FYPO:0006855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0002274","FYPO:0000002","FYPO:0002494"],"is_obsolete":false,"name":"decreased histone H3-K37 methylation","synonyms":[{"name":"decreased histone H3 K37 methylation","type":"exact"},{"name":"decreased histone H3K37me","type":"exact"},{"name":"decreased histone lysine H3 K37 methylation","type":"exact"},{"name":"reduced histone H3-K37 trimethylation","type":"exact"}],"termid":"FYPO:0006857"}


id: PBO:0056898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"migration and invasion enhancer 1","termid":"PBO:0056898"}


id: PR:O60069
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- swf1 gene.","definition_xrefs":["UniProtKB:O60069","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":"palmitoyltransferase swf1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC13G1.07","synonyms":[{"name":"Spom972h-swf1","type":"exact"}],"termid":"PR:O60069"}


id: PBO:0027192
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cytoplasmic_microtubules_nucleated_from_equatorial_microtubule_organizing_center_present_in_decreased_numbers","termid":"PBO:0027192"}


id: PBO:0090730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S12 Mrps12a","termid":"PBO:0090730"}


id: PATO:0000212
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000212 neural function (obsolete PATO:0000212)","termid":"PATO:0000212"}


id: GO:0086087
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a potassium ion by a voltage-gated channel through the plasma membrane of a bundle of His cell contributing to the repolarization phase of an action potential. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel activity involved in cardiac muscle cell action potential repolarization","termid":"GO:0086008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"voltage-gated potassium channel activity involved in bundle of His cell action potential repolarization","termid":"GO:0086087"}


id: PBO:0051114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 1-69-2","termid":"PBO:0051114"}


id: PBO:0031389
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_methionine","termid":"PBO:0031389"}


id: PBO:0049040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 32","termid":"PBO:0049040"}


id: PBO:0000997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP1/OBG family","termid":"PBO:0000997"}


id: PBO:0073716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-phase kinase associated protein 1 pseudogene 3","termid":"PBO:0073716"}


id: GO:1902807
data:
  {"annotated_genes":["SJAG_03591","SJAG_02026","SJAG_00991","SJAG_01210","SJAG_00169","SJAG_01401","SJAG_00071","SJAG_05346","SJAG_00996","SJAG_03048","SJAG_03681"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103577,90888,110868,117901,104313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031568"},{"annotations":[111653,93255],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[100827,94106,93692,95274],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000134"}]},"cv_name":"biological_process","definition":"Any signaling pathway that decreases or inhibits the activity of a cell cycle cyclin-dependent protein kinase to modulate the switch from G1 phase to S phase of the cell cycle.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell cycle phase transition","termid":"GO:1901988"},{"relation_name":"is_a","term_name":"regulation of cell cycle G1/S phase transition","termid":"GO:1902806"},{"relation_name":"negatively_regulates","term_name":"cell cycle G1/S phase transition","termid":"GO:0044843"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00169":null,"SJAG_00991":null,"SJAG_00996":null,"SJAG_01210":null,"SJAG_01401":null,"SJAG_02026":null,"SJAG_03048":null,"SJAG_03591":null,"SJAG_03681":null,"SJAG_05346":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"negative regulation of cell cycle G1/S phase transition","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of cell cycle G1/S phase transition","type":"exact"},{"name":"down-regulation of cell cycle G1/S phase transition","type":"exact"},{"name":"downregulation of cell cycle G1/S phase transition","type":"exact"},{"name":"inhibition of cell cycle G1/S phase transition","type":"narrow"}],"termid":"GO:1902807","terms_by_termid":{"GO:0031568":null,"GO:0031571":null,"GO:2000134":null}}


id: MONDO:0100469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked form of anosmia, isolated congenital.","definition_xrefs":["MONDO:patterns/x_linked"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anosmia","termid":"MONDO:0010528"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anosmia, isolated congenital, X-linked","secondary_identifiers":["UMLS:C5562112","MEDGEN:1794322","OMIM:301700"],"termid":"MONDO:0100469","xrefs":{"Monarch":{"xref_id":"0100469"}}}


id: GO:0019005
data:
  {"annotated_genes":["SJAG_00439","SJAG_00192","SJAG_03651","SJAG_00615","SJAG_02591","SJAG_00341","SJAG_02822","SJAG_03219","SJAG_02162","SJAG_02044","SJAG_01022","SJAG_02651"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[61427,75959,82225,90509,97491,104823],"is_not":false,"summary":null,"term":"GO:0019005"},{"annotations":[96293,111055,106829,112306,99720,92546],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043224"}]},"cv_name":"cellular_component","definition":"A ubiquitin ligase complex in which a cullin from the Cul1 subfamily and a RING domain protein form the catalytic core; substrate specificity is conferred by a Skp1 adaptor and an F-box protein. SCF complexes are involved in targeting proteins for degradation by the proteasome. The best characterized complexes are those from yeast and mammals (with core subunits named Cdc53/Cul1, Rbx1/Hrt1/Roc1).","definition_xrefs":["PMID:15688063","PMID:15571813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cullin-RING ubiquitin ligase complex","termid":"GO:0031461"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00192":null,"SJAG_00341":null,"SJAG_00439":null,"SJAG_00615":null,"SJAG_01022":null,"SJAG_02044":null,"SJAG_02162":null,"SJAG_02591":null,"SJAG_02651":null,"SJAG_02822":null,"SJAG_03219":null,"SJAG_03651":null},"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":"SCF ubiquitin ligase complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Wikipedia:SCF_complex"],"synonyms":[{"name":"CDL1 complex","type":"exact"},{"name":"CRL1 complex","type":"exact"},{"name":"Cul1-RING ubiquitin ligase complex","type":"exact"},{"name":"SCF complex","type":"exact"},{"name":"SCF complex substrate recognition subunit","type":"narrow"},{"name":"Skp1/Cul1/F-box protein complex","type":"exact"},{"name":"cullin-RING ligase 1","type":"exact"}],"termid":"GO:0019005","terms_by_termid":{"GO:0019005":null,"GO:0043224":null}}


id: MONDO:0001388
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the glans penis.","direct_ancestors":[{"relation_name":"is_a","term_name":"penile cancer","termid":"MONDO:0001325"}],"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":"glans penis cancer","secondary_identifiers":["UMLS:C0153599","ICD9:187.2","NCIT:C194357","DOID:11839","MEDGEN:509337","ICD10CM:C60.1","SCTID:363451005"],"synonyms":[{"name":"cancer of glans penis","type":"exact"},{"name":"glans penis cancer","type":"exact"},{"name":"malignant glans penis neoplasm","type":"exact"},{"name":"malignant neoplasm of glans penis","type":"exact"},{"name":"malignant tumor of glans penis","type":"exact"},{"name":"malignant tumour of glans penis","type":"exact"}],"termid":"MONDO:0001388","xrefs":{"Monarch":{"xref_id":"0001388"}}}


id: GO:0042594
data:
  {"annotated_genes":["SJAG_00457","SJAG_02292","SJAG_01245","SJAG_02973","SJAG_03309","SJAG_00380","SJAG_03048","SJAG_00209","SJAG_02785","SJAG_00233","SJAG_02380","SJAG_01970","SJAG_04031","SJAG_04677","SJAG_02389","SJAG_03519","SJAG_02474","SJAG_03486","SJAG_00845","SJAG_04873","SJAG_00534","SJAG_00256","SJAG_04067","SJAG_02878","SJAG_04743","SJAG_01184","SJAG_01509","SJAG_01885","SJAG_03602","SJAG_02331","SJAG_00169","SJAG_02424","SJAG_04032","SJAG_02026","SJAG_03371","SJAG_02699","SJAG_00781"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75542,97174,74023,75886,96628,73427,77789,63078],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034198"},{"annotations":[100377,102397,59149,77972,71903,77939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042149"},{"annotations":[79604,102445,96058,114790,59795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010106"},{"annotations":[74123,109546,115334,115335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016036"},{"annotations":[79071,76612,82305,80218,96576,74420,78329,73517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009267"},{"annotations":[117587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031142"},{"annotations":[71248,68283],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903833"},{"annotations":[89797,103348],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905287"},{"annotations":[104342],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1904547"}]},"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 starvation stimulus, deprivation of nourishment.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"response to nutrient levels","termid":"GO:0031667"}],"gene_count":37,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00209":null,"SJAG_00233":null,"SJAG_00256":null,"SJAG_00380":null,"SJAG_00457":null,"SJAG_00534":null,"SJAG_00781":null,"SJAG_00845":null,"SJAG_01184":null,"SJAG_01245":null,"SJAG_01509":null,"SJAG_01885":null,"SJAG_01970":null,"SJAG_02026":null,"SJAG_02292":null,"SJAG_02331":null,"SJAG_02380":null,"SJAG_02389":null,"SJAG_02424":null,"SJAG_02474":null,"SJAG_02699":null,"SJAG_02785":null,"SJAG_02878":null,"SJAG_02973":null,"SJAG_03048":null,"SJAG_03309":null,"SJAG_03371":null,"SJAG_03486":null,"SJAG_03519":null,"SJAG_03602":null,"SJAG_04031":null,"SJAG_04032":null,"SJAG_04067":null,"SJAG_04677":null,"SJAG_04743":null,"SJAG_04873":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to starvation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0042594","terms_by_termid":{"GO:0009267":null,"GO:0010106":null,"GO:0016036":null,"GO:0031142":null,"GO:0034198":null,"GO:0042149":null,"GO:1903833":null,"GO:1904547":null,"GO:1905287":null}}


id: GO:0046877
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of saliva from a cell or a tissue.","definition_xrefs":["GOC:ai"],"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":"saliva secretion","termid":"GO:0046541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of saliva secretion","termid":"GO:0046877"}


id: GO:0061655
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Isoenergetic transfer of Pup from one protein to another via the reaction X-Pup + Y = Y-Pup + X, where both the X-Pup and Y-Pup linkages are thioester bonds between the C-terminal amino acid of Pup and a sulfhydryl side group of a cysteine residue.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein conjugating enzyme activity","termid":"GO:0061650"},{"relation_name":"is_a","term_name":"Pup transferase activity","termid":"GO:0072496"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"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:0019787","GO:0003674","GO:0140096","GO:0016746","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"Pup conjugating enzyme activity","synonyms":[{"name":"E2","type":"broad"}],"termid":"GO:0061655"}


id: PBO:0046459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidermal growth factor receptor pathway substrate 15 pseudogene 1","termid":"PBO:0046459"}


id: PBO:0030958
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_dimethylation_at_centromere_outer_repeat","termid":"PBO:0030958"}


id: FYPO:0007216
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 chromatin at promoters that contain MCB sites is abolished  during a cellular response to hydroxyurea.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to chromatin at MCB promoters","termid":"FYPO:0005460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to chromatin at MCB promoters during cellular response to hydroxyurea","synonyms":[{"name":"abolished protein localisation to chromatin at MCB promoters during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"abolished protein localization to chromatin at MCB promoters during cellular response to HU","type":"exact"},{"name":"abolished protein localization to chromatin at MCB promoters during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to chromatin at MCB target genes during cellular response to hydroxyurea","type":"related"},{"name":"abolished protein localization to chromatin at MCB-containing promoters during cellular response to hydroxyurea","type":"exact"},{"name":"protein localization to chromatin at MCB promoters during vegetative growth abolished during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0007216"}


id: PR:O43018
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC354.04 gene.","definition_xrefs":["UniProtKB:O43018","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 C354.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC354.04","synonyms":[{"name":"Spom972h-SPBC354.04","type":"exact"}],"termid":"PR:O43018"}


id: GO:0004510
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-tryptophan + tetrahydrobiopterin + O2 = 5-hydroxy-L-tryptophan + 4-alpha-hydroxytetrahydrobiopterin + H2O.","definition_xrefs":["EC:1.14.16.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen","termid":"GO:0016714"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"tryptophan 5-monooxygenase activity","secondary_identifiers":["Reactome:R-HSA-209828","RHEA:16709","MetaCyc:TRYPTOPHAN-5-MONOOXYGENASE-RXN"],"synonyms":[{"name":"L-tryptophan hydroxylase activity","type":"exact"},{"name":"L-tryptophan,tetrahydrobiopterin:oxygen oxidoreductase (5-hydroxylating)","type":"related"},{"name":"indoleacetic acid-5-hydroxylase activity","type":"related"},{"name":"tryptophan 5-hydroxylase activity","type":"related"},{"name":"tryptophan hydroxylase activity","type":"related"}],"termid":"GO:0004510"}


id: GO:0046829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the movement of RNA from the cytoplasm into the nucleus.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nucleobase-containing compound transport","termid":"GO:0032240"},{"relation_name":"is_a","term_name":"negative regulation of nucleocytoplasmic transport","termid":"GO:0046823"},{"relation_name":"is_a","term_name":"regulation of RNA import into nucleus","termid":"GO:0046828"},{"relation_name":"negatively_regulates","term_name":"RNA import into nucleus","termid":"GO:0006404"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006913"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006913"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006913","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of RNA import into nucleus","synonyms":[{"name":"down regulation of RNA import into nucleus","type":"exact"},{"name":"down-regulation of RNA import into nucleus","type":"exact"},{"name":"downregulation of RNA import into nucleus","type":"exact"},{"name":"inhibition of RNA import into nucleus","type":"narrow"},{"name":"negative regulation of RNA import into cell nucleus","type":"exact"},{"name":"negative regulation of RNA transport from cytoplasm to nucleus","type":"exact"},{"name":"negative regulation of RNA-nucleus import","type":"exact"}],"termid":"GO:0046829"}


id: MONDO:0017717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete metabolic disease due to other fatty acid oxidation disorder (obsolete MONDO:0017717)","secondary_identifiers":["Orphanet:309133"],"termid":"MONDO:0017717","xrefs":{"Monarch":{"xref_id":"0017717"}}}


id: GO:0098897
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding the spine apparatus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bounding membrane of organelle","termid":"GO:0098588"},{"relation_name":"part_of","term_name":"spine apparatus","termid":"GO:0097444"}],"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":"spine apparatus membrane","termid":"GO:0098897"}


id: PBO:0058222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4512","termid":"PBO:0058222"}


id: MONDO:0008191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete human papillomavirus type 18 integration site 2 (obsolete MONDO:0008191)","secondary_identifiers":["OMIM:167960"],"termid":"MONDO:0008191","xrefs":{"Monarch":{"xref_id":"0008191"}}}


id: PBO:0109454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LHX8 antisense RNA 1","termid":"PBO:0109454"}


id: FYPO:0002377
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 viable and has a larger volume than normal. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"swollen vegetative cell","termid":"FYPO:0000646"},{"relation_name":"has_part","term_name":"viable vegetative cell","termid":"FYPO:0001491"},{"relation_name":"is_a","term_name":"swollen vegetative cell","termid":"FYPO:0000646"},{"relation_name":"is_a","term_name":"viable vegetative cell","termid":"FYPO:0001491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000004","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"viable swollen vegetative cell","synonyms":[{"name":"viable enlarged vegetative cell","type":"related"},{"name":"viable large vegetative cell","type":"related"},{"name":"viable swollen cell during vegetative growth","type":"exact"},{"name":"viable swollen vegetative cell during mitotic cell cycle","type":"related"},{"name":"viable vegetative cell with increased cell size","type":"related"},{"name":"viable vegetative cell with increased cell volume","type":"exact"}],"termid":"FYPO:0002377"}


id: MONDO:0002788
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A craniopharyngioma composed of sheets of squamous epithelium which separate to form pseudopapillae. This variant typically lacks nuclear palisading, wet keratin, calcification, and cholesterol deposits. Clinically, endocrine deficiencies are more often associated with papillary craniopharyngioma than with the adamantinomatous type. (Adapted from WHO)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"craniopharyngioma","termid":"MONDO:0018907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papillary craniopharyngioma","secondary_identifiers":["NCIT:C4725","ICDO:9352/1","UMLS:C0431128","DOID:3847","MEDGEN:98125"],"synonyms":[{"name":"craniopharyngioma, papillary","type":"exact"},{"name":"craniopharyngioma, papillary (morphologic abnormality)","type":"exact"},{"name":"papillary Rathke pouch neoplasm","type":"exact"},{"name":"papillary Rathke's pouch neoplasm","type":"exact"},{"name":"papillary Rathke's pouch tumor","type":"exact"},{"name":"papillary Rathke's pouch tumour","type":"exact"},{"name":"papillary craniopharyngioma (morphologic abnormality)","type":"exact"},{"name":"papillary neoplasm of Rathke's pouch","type":"exact"},{"name":"papillary tumor of Rathke's pouch","type":"exact"},{"name":"papillary tumour of Rathke's pouch","type":"exact"}],"termid":"MONDO:0002788","xrefs":{"Monarch":{"xref_id":"0002788"}}}


id: PBO:0016053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor, Prp19 complex subunit Cdc5","termid":"PBO:0016053"}


id: PBO:0071183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 24","termid":"PBO:0071183"}


id: PBO:0036458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smaug family RNA binding protein involved in CCR4-NOT dependent deadenylation (predicted)","termid":"PBO:0036458"}


id: GO:0021782
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a glial cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:dgh","GOC:dph","GOC:cls","GO_REF:0000021","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"},{"relation_name":"part_of","term_name":"glial cell differentiation","termid":"GO:0010001"}],"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":"glial cell development","termid":"GO:0021782"}


id: GO:0000723
data:
  {"annotated_genes":["SJAG_05173","SJAG_02563","SJAG_02212","SJAG_04372","SJAG_04183","SJAG_01068","SJAG_05979","SJAG_01864","SJAG_03780","SJAG_03624","SJAG_01263","SJAG_06597","SJAG_00364","SJAG_03720","SJAG_02116","SJAG_05372","SJAG_01377","SJAG_01777","SJAG_03685","SJAG_00429","SJAG_01605","SJAG_01832","SJAG_00559","SJAG_04245","SJAG_04150","SJAG_02079","SJAG_05105","SJAG_04586","SJAG_01378","SJAG_03026","SJAG_00640","SJAG_00939","SJAG_04266","SJAG_01677","SJAG_01410","SJAG_03843","SJAG_03092","SJAG_05373","SJAG_02194","SJAG_02362","SJAG_05353","SJAG_04863","SJAG_03722","SJAG_06642","SJAG_03855","SJAG_02771"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59366,65297,72217,72937,73527,73568,80248,80809,81268,91069,93381,101143,102818,106113,107924,109728,110012,111364,111541,113525,114825,118254,118850],"is_not":false,"summary":null,"term":"GO:0000723"},{"annotations":[99132],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0032215"},{"annotations":[91715,81735],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0031848"},{"annotations":[78937],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032210"},{"annotations":[117943,112360,78936,64444,101675,93789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016233"},{"annotations":[98134,82098,114941,113726,114940,114942,114939,114938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000722"},{"annotations":[82103,71531,92584,117945,72564,82166,110094,115822],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007004"},{"annotations":[93791,81733,76012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010833"}]},"cv_name":"biological_process","definition":"Any process that contributes to the maintenance of proper telomeric length and structure by affecting and monitoring the activity of telomeric proteins, the length of telomeric DNA and the replication and repair of the DNA. These processes includes those that shorten, lengthen, replicate and repair the telomeric DNA sequences.","definition_xrefs":["GOC:rl","PMID:11092831","GOC:BHF","GOC:BHF_telomere","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolic process","termid":"GO:0006259"},{"relation_name":"is_a","term_name":"telomere organization","termid":"GO:0032200"}],"gene_count":46,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_00429":null,"SJAG_00559":null,"SJAG_00640":null,"SJAG_00939":null,"SJAG_01068":null,"SJAG_01263":null,"SJAG_01377":null,"SJAG_01378":null,"SJAG_01410":null,"SJAG_01605":null,"SJAG_01677":null,"SJAG_01777":null,"SJAG_01832":null,"SJAG_01864":null,"SJAG_02079":null,"SJAG_02116":null,"SJAG_02194":null,"SJAG_02212":null,"SJAG_02362":null,"SJAG_02563":null,"SJAG_02771":null,"SJAG_03026":null,"SJAG_03092":null,"SJAG_03624":null,"SJAG_03685":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03780":null,"SJAG_03843":null,"SJAG_03855":null,"SJAG_04150":null,"SJAG_04183":null,"SJAG_04245":null,"SJAG_04266":null,"SJAG_04372":null,"SJAG_04586":null,"SJAG_04863":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_05979":null,"SJAG_06597":null,"SJAG_06642":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0032200"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0032200"],"is_obsolete":false,"name":"telomere maintenance","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-157579"],"synonyms":[{"name":"regulation of telomere length","type":"related"}],"termid":"GO:0000723","terms_by_termid":{"GO:0000722":null,"GO:0000723":null,"GO:0007004":null,"GO:0010833":null,"GO:0016233":null,"GO:0031848":null,"GO:0032210":null,"GO:0032215":null}}


id: PBO:0012299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human LYAR homolog","termid":"PBO:0012299"}


id: PR:C6Y4D2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrp49 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4D2"],"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":"54S ribosomal protein MRP49, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1442.19","synonyms":[{"name":"Spom972h-mrp49","type":"exact"}],"termid":"PR:C6Y4D2"}


id: GO:0075048
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process in which the cell wall of the symbiont is strengthened or thickened during penetration into the body, tissues, or cells of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cell wall strengthening in symbiont involved in entry into host (obsolete GO:0075048)","synonyms":[{"name":"cell wall strengthening in symbiont during entry into host","type":"related"},{"name":"cell wall thickening in symbiont during entry into host","type":"related"},{"name":"symbiont cell wall strengthening during entry into host","type":"related"}],"termid":"GO:0075048"}


id: GO:0046024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of transcription from an RNA polymerase III that occurs during the mitotic cell cycle.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase III promoter during mitotic cell cycle (obsolete GO:0046024)","synonyms":[{"name":"activation of transcription from RNA polymerase III promoter during mitosis","type":"narrow"},{"name":"mitotic activation of transcription from Pol III promoter","type":"exact"},{"name":"positive regulation of transcription from Pol III promoter during mitosis","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase III promoter, mitotic","type":"exact"},{"name":"stimulation of transcription from RNA polymerase III promoter during mitosis","type":"narrow"},{"name":"up regulation of transcription from RNA polymerase III promoter during mitosis","type":"exact"},{"name":"up-regulation of transcription from RNA polymerase III promoter during mitosis","type":"exact"},{"name":"upregulation of transcription from RNA polymerase III promoter during mitosis","type":"exact"}],"termid":"GO:0046024"}


id: MONDO:0017287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A recently described mass-forming lesion that occurs in the pancreas, submandibular glands, lacrimal glands, lymph nodes, and hepatobiliary tract. It is characterized by the presence of marked tissue sclerosis and infiltration by numerous plasma cells. The plasma cells show immunohistochemical staining for IgG4 and the serum IgG4 levels are often increased.","definition_xrefs":["NCIT:C95992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"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":"immunoglobulin G4-related sclerosing disease","secondary_identifiers":["Orphanet:284264","UMLS:C3203653","MEDGEN:473761","MedDRA:10071569","DOID:0080356","Orphanet:596448","NANDO:1200923","GARD:12521","NANDO:1200924","icd11.foundation:99883782"],"synonyms":[{"name":"IgG4-RD","type":"exact"},{"name":"IgG4-associated disease","type":"related"},{"name":"IgG4-positive multiorgan lymphoproliferative syndrome","type":"related"},{"name":"IgG4-related autoimmune disease","type":"related"},{"name":"IgG4-related disease","type":"exact"},{"name":"IgG4-related sclerosing disease","type":"exact"},{"name":"IgG4-related systemic disease","type":"exact"},{"name":"IgG4-related systemic sclerosing disease","type":"related"},{"name":"IgG4-syndrome","type":"related"},{"name":"hyper-IgG4 disease","type":"related"},{"name":"immunoglobulin G4-related sclerosing disease","type":"exact"},{"name":"multifocal fibrosclerosis","type":"related"},{"name":"multifocal idiopathic fibrosclerosis","type":"related"},{"name":"systemic IgG4-related plasmacytic syndrome","type":"related"},{"name":"systemic IgG4-related sclerosing syndrome","type":"related"}],"termid":"MONDO:0017287","xrefs":{"Monarch":{"xref_id":"0017287"}}}


id: MONDO:0018661
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mosquito-born virus disease characterized by a clinical course that may be asymptomatic or mild with fever, conjunctivitis, muscle and joint pain, headache, exanthema, but may also be associated with severe neurological (meningitis, meningoencephalitis and myelitis) and auto-immune (Guillain-Barre syndrome) complications, as well as a potential increase of birth defects (microcephaly) if the infection occurs during pregnancy.","definition_xrefs":["Orphanet:448237"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Flaviviridae infectious disease","termid":"MONDO:0005763"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zika virus infectious disease","secondary_identifiers":["DOID:0060478","MEDGEN:547236","UMLS:C0276289","NCIT:C128423","icd11.foundation:1401438580","ICD10CM:A92.5","MESH:D000071243","GARD:12894","SCTID:3928002"],"synonyms":[{"name":"ZikV infection","type":"exact"},{"name":"Zika","type":"exact"},{"name":"Zika fever","type":"related"},{"name":"Zika virus caused disease or disorder","type":"exact"},{"name":"Zika virus disease","type":"exact"},{"name":"Zika virus disease or disorder","type":"exact"},{"name":"Zika virus infection","type":"exact"},{"name":"Zika virus infectious disease","type":"exact"},{"name":"congenital Zika syndrome","type":"narrow"},{"name":"congenital Zika virus infection","type":"narrow"},{"name":"fever, Zika","type":"related"}],"termid":"MONDO:0018661","xrefs":{"Monarch":{"xref_id":"0018661"}}}


id: PBO:0028991
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_proline_import","termid":"PBO:0028991"}


id: GO:0003390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of a dendrite over time by the attachment of a part of the neuron to an anchor and the subsequent migration of the cell body away from the anchor point.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retrograde extension","termid":"GO:0003389"},{"relation_name":"is_a","term_name":"dendrite development","termid":"GO:0016358"}],"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":"dendrite development by retrograde extension","synonyms":[{"name":"dendrite retrograde extension","type":"exact"}],"termid":"GO:0003390"}


id: GO:0043731
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the oxidative decarboxylation of 6-hydroxynicotinate to 2,5-dihydroxypyridine, dependent on O2, NADH +H+ and FAD.","definition_xrefs":["GOC:jl","PMID:10091591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"6-hydroxynicotinate 3-monooxygenase activity","secondary_identifiers":["EC:1.14.13.114","MetaCyc:RXN-7573","RHEA:27333"],"termid":"GO:0043731"}


id: GO:0044012
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H2A L-lysine (position 9) = CoA + histone H2A N6-acetyl-L-lysine (position 9).","definition_xrefs":["PMID:18552846"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2A acetyltransferase activity","termid":"GO:0043998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0034212","GO:0140096","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"histone H2AK9 acetyltransferase activity","synonyms":[{"name":"histone H2A-K9 acetyltransferase activity","type":"exact"},{"name":"histone acetylase activity (H2A-K9 specific)","type":"exact"},{"name":"histone acetyltransferase activity (H2A-K9 specific)","type":"exact"},{"name":"histone lysine N-acetyltransferase activity (H2A-K9 specific)","type":"exact"}],"termid":"GO:0044012"}


id: PBO:0062866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OTU deubiquitinase 4","termid":"PBO:0062866"}


id: GO:0050297
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-dopa + O2 = 4-(L-alanin-3-yl)-2-hydroxy-cis,cis-muconate 6-semialdehyde + H+.","definition_xrefs":["RHEA:21220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"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:0003824","GO:0016491"],"is_obsolete":false,"name":"stizolobate synthase activity","secondary_identifiers":["MetaCyc:RXN-8460","EC:1.13.11.29"],"synonyms":[{"name":"3,4-dihydroxy-L-phenylalanine:oxygen 4,5-oxidoreductase (recyclizing)","type":"related"},{"name":"DOPA dioxygenase activity","type":"exact"}],"termid":"GO:0050297"}


id: PBO:0027230
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_diglyceride_level","termid":"PBO:0027230"}


id: PBO:0002953
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmental disorders","termid":"PBO:0002953"}


id: FYPO:0000739
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype that affects the occurrence of pigment accumulation in a cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process phenotype during vegetative growth","termid":"FYPO:0001331"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"cellular pigment accumulation phenotype","synonyms":[{"name":"cellular pigment accumulation phenotype during mitotic cell cycle","type":"related"},{"name":"cellular pigment accumulation phenotype during vegetative growth","type":"exact"},{"name":"fission yeast cellular pigment accumulation phenotype","type":"exact"}],"termid":"FYPO:0000739"}


id: PBO:0041493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 12 open reading frame 43","termid":"PBO:0041493"}


id: PBO:0043394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X9-C motif containing 1","termid":"PBO:0043394"}


id: GO:0097519
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein-DNA complex consisting of a higher-order oligomer of strand exchange proteins (recombinases) on single-stranded DNA.","definition_xrefs":["GOC:cjm","PMID:10357855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex","termid":"GO:0032993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"DNA recombinase complex","termid":"GO:0097519"}


id: PBO:0052933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 21-1","termid":"PBO:0052933"}


id: MONDO:0004208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant smooth muscle neoplasm, arising from the superior vena cava. It is characterized by a proliferation of neoplastic spindle cells.","definition_xrefs":["NCIT:C6745"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"pulmonary artery leiomyosarcoma","termid":"MONDO:0004207"},{"relation_name":"is_a","term_name":"superior vena cava angiosarcoma","termid":"MONDO:0003032"},{"relation_name":"is_a","term_name":"leiomyosarcoma","termid":"MONDO:0005058"}],"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":"superior vena cava leiomyosarcoma","secondary_identifiers":["DOID:7390","MEDGEN:236963","UMLS:C1336531"],"synonyms":[{"name":"anterior vena cava leiomyosarcoma","type":"exact"},{"name":"leiomyosarcoma of Superior vena cava","type":"exact"},{"name":"leiomyosarcoma of anterior vena cava","type":"exact"},{"name":"leiomyosarcoma of the Superior vena cava","type":"exact"}],"termid":"MONDO:0004208","xrefs":{"Monarch":{"xref_id":"0004208"}}}


id: PBO:0072002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S7 pseudogene 4","termid":"PBO:0072002"}


id: PBO:0047388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 27","termid":"PBO:0047388"}


id: PBO:0056617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MDS1 and EVI1 complex locus","termid":"PBO:0056617"}


id: PBO:0040942
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 13","termid":"PBO:0040942"}


id: MONDO:1010013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cor triatriatum dexter that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cor triatriatum dexter, non-human animal","secondary_identifiers":["OMIA:000227"],"termid":"MONDO:1010013","xrefs":{"Monarch":{"xref_id":"1010013"}}}


id: PBO:0089201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human REX1BD ortholog, implicated in DNA repair","termid":"PBO:0089201"}


id: PBO:0111863
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1 domain","termid":"PBO:0111863"}


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: MONDO:0018965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies.","definition_xrefs":["Orphanet:63"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete lens shape anomaly (obsolete MONDO:0020237)","termid":"MONDO:0020237"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary nephritis","termid":"MONDO:0005334"}],"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":"Alport syndrome","secondary_identifiers":["NORD:756","NCIT:C34842","DOID:10983","ICD10CM:Q87.81","icd11.foundation:1170919425","GARD:5785","MEDGEN:339209","MESH:D009394","NANDO:2200126","NANDO:1200712","OMIMPS:301050","MedDRA:10001843","UMLS:C1567741"],"synonyms":[{"name":"Alport deafness-nephropathy","type":"exact"},{"name":"Alport syndrome","type":"exact"},{"name":"Alport's syndrome","type":"exact"},{"name":"hereditary nephritis","type":"broad"}],"termid":"MONDO:0018965","xrefs":{"Monarch":{"xref_id":"0018965"}}}


id: GO:0032163
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A septin band, i.e. a diffuse ring composed of a series of septin bars running parallel to the long axis of the cell, located at the junction between the mother cell and the germ tube (hypha) of a fungal cell growing filamentously.","definition_xrefs":["GOC:krc","GOC:mah","PMID:16151244"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septin band","termid":"GO:0032158"}],"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":"hyphal septin band","termid":"GO:0032163"}


id: PBO:0084238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Import and assembly protein in mitochondrial intermembrane space; component of MIA pathway which mediates import and oxidative folding of substrates including small proteins containing twin cysteine motifs; acts in concert with Erv1p, which oxidizes the cysteine residues of Mia40p to comprise a disulfide relay system that catalyzes import; also mediates folding of Atp23p via a chaperone-like activity; forms a dimer that binds iron-sulfur cluster in vitro","termid":"PBO:0084238"}


id: MONDO:0006126
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the cecum. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent.","definition_xrefs":["NCIT:C5501"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cecal neoplasm","termid":"MONDO:0005694"},{"relation_name":"is_a","term_name":"colon neuroendocrine tumor G1","termid":"MONDO:0006155"}],"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":"cecum neuroendocrine tumor G1","secondary_identifiers":["UMLS:C0854488","MEDGEN:167703"],"synonyms":[{"name":"caecal carcinoid tumor","type":"exact"},{"name":"caecal carcinoid tumour","type":"exact"},{"name":"caecum NET G1","type":"exact"},{"name":"caecum carcinoid tumor","type":"exact"},{"name":"caecum carcinoid tumor (disease)","type":"exact"},{"name":"caecum carcinoid tumour","type":"exact"},{"name":"caecum carcinoid tumour (disease)","type":"exact"},{"name":"caecum neuroendocrine neoplasm G1","type":"exact"},{"name":"caecum neuroendocrine tumor, well differentiated, low grade","type":"exact"},{"name":"carcinoid tumor of cecum","type":"exact"},{"name":"carcinoid tumor of the cecum","type":"exact"},{"name":"carcinoid tumour of cecum","type":"exact"},{"name":"carcinoid tumour of the cecum","type":"exact"},{"name":"cecal carcinoid tumor","type":"exact"},{"name":"cecal carcinoid tumour","type":"exact"},{"name":"cecum NET G1","type":"exact"},{"name":"cecum carcinoid tumor","type":"exact"},{"name":"cecum carcinoid tumour","type":"exact"},{"name":"cecum neuroendocrine tumor G1","type":"exact"},{"name":"grade 1 neuroendocrine neoplasm of caecum","type":"exact"}],"termid":"MONDO:0006126","xrefs":{"Monarch":{"xref_id":"0006126"}}}


id: GO:0072365
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of a cellular ketone metabolic process by stopping, preventing, or reducing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:mah","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular ketone metabolic process by negative regulation of transcription from RNA polymerase II promoter (obsolete GO:0072365)","synonyms":[{"name":"regulation of cellular ketone metabolic process by negative regulation of transcription from an RNA polymerase II promoter","type":"exact"},{"name":"regulation of cellular ketone metabolism by negative regulation of transcription from an RNA polymerase II promoter","type":"exact"}],"termid":"GO:0072365"}


id: PBO:0087573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of TFIIH complex; involved in transcription initiation, similar to 34 kDa subunit of human TFIIH; interacts with Ssl1p","termid":"PBO:0087573"}


id: GO:0009659
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 leucoplast. A leucoplast is a colorless plastid involved in the synthesis of monoterpenes.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid organization","termid":"GO:0009657"}],"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":"leucoplast organization","synonyms":[{"name":"leucoplast organisation","type":"exact"},{"name":"leucoplast organization and biogenesis","type":"related"}],"termid":"GO:0009659"}


id: MONDO:0002552
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spinal cord disorder","termid":"MONDO:0002545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular myelopathy","secondary_identifiers":["UMLS:C0154685","ICD10CM:G95.1","DOID:320","ICD9:336.1","MEDGEN:509629","SCTID:29774004"],"synonyms":[{"name":"vascular myelopathies","type":"exact"}],"termid":"MONDO:0002552","xrefs":{"Monarch":{"xref_id":"0002552"}}}


id: MONDO:0017190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sporadic pheochromocytoma/secreting paraganglioma are isolated, non-familial, catecholamin-producing tumors arising from neuroendocrine chromaffin cells in the adrenal medulla or in extra-adrenal chromaffin tissue, respectively. The majority of these tumors are benign and the presenting symptoms are typically caused by the increased catecholamine production of the tumor, including hypertension (often paroxysmal), tachycardia, anxiety and/or excessive sweating.","definition_xrefs":["Orphanet:276621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paraganglioma","termid":"MONDO:0000448"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sporadic pheochromocytoma/secreting paraganglioma","secondary_identifiers":["MEDGEN:1636854","UMLS:C4707333","GARD:7385"],"termid":"MONDO:0017190","xrefs":{"Monarch":{"xref_id":"0017190"}}}


id: MONDO:0015943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Eosinophilic granulomatosis with polyangiitis (EGPA), previously known as Churg-Strauss syndrome, is a systemic vasculitis of small-to medium vessels, characterized by asthma, transient pulmonary infiltrates, and hypereosinophilia.","definition_xrefs":["Orphanet:183"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete systemic inflammatory disease associated with an acquired peripheral neuropathy (obsolete MONDO:0016177)","termid":"MONDO:0016177"},{"relation_name":"excluded_subClassOf","term_name":"obsolete non-familial rare disease with dilated cardiomyopathy (obsolete MONDO:0017952)","termid":"MONDO:0017952"},{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"granulomatosis with polyangiitis","termid":"MONDO:0012105"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0005046"],"is_obsolete":false,"name":"eosinophilic granulomatosis with polyangiitis","secondary_identifiers":["NANDO:1200264","icd11.foundation:835880885","NCIT:C34481","ICD10CM:M30.1","DOID:3049","EFO:0007208","GARD:6111","MedDRA:10048594","MEDGEN:3088","MESH:D015267","NANDO:2200427","NORD:973","UMLS:C0008728","SCTID:82275008"],"synonyms":[{"name":"CSS","type":"exact"},{"name":"Churg Strauss Syndrome","type":"exact"},{"name":"Churg Strauss syndrome","type":"exact"},{"name":"Churg-Strauss syndrome","type":"exact"},{"name":"Churg-Strauss vasculitis","type":"exact"},{"name":"EGPA","type":"exact"},{"name":"allergic angiitides","type":"exact"},{"name":"allergic angiitides, granulomatous","type":"exact"},{"name":"allergic angiitis","type":"exact"},{"name":"allergic angiitis and granulomatosis","type":"exact"},{"name":"allergic angiitis, granulomatous","type":"exact"},{"name":"allergic granulomatoses","type":"exact"},{"name":"allergic granulomatosis","type":"exact"},{"name":"allergic granulomatosis angiitis","type":"exact"},{"name":"allergic granulomatous Angiitides","type":"exact"},{"name":"allergic granulomatous and angiitis","type":"exact"},{"name":"allergic granulomatous angiitis","type":"exact"},{"name":"angiitides, allergic","type":"exact"},{"name":"angiitides, allergic granulomatous","type":"exact"},{"name":"angiitides, granulomatous allergic","type":"exact"},{"name":"angiitis, allergic","type":"exact"},{"name":"angiitis, allergic granulomatous","type":"exact"},{"name":"angiitis, granulomatous allergic","type":"exact"},{"name":"eosinophilic granulomatous Vasculitides","type":"exact"},{"name":"eosinophilic granulomatous vasculitis","type":"exact"},{"name":"granulomatoses, allergic","type":"exact"},{"name":"granulomatosis, allergic","type":"exact"},{"name":"granulomatous allergic Angiitides","type":"exact"},{"name":"granulomatous allergic angiitis","type":"exact"},{"name":"granulomatous angiitides, allergic","type":"exact"},{"name":"granulomatous angiitis, allergic","type":"exact"},{"name":"granulomatous vasculitides, eosinophilic","type":"exact"},{"name":"granulomatous vasculitis, eosinophilic","type":"exact"},{"name":"syndrome, Churg-Strauss","type":"exact"},{"name":"vasculitides, eosinophilic granulomatous","type":"exact"},{"name":"vasculitis, Churg Strauss","type":"exact"},{"name":"vasculitis, Churg-Strauss","type":"exact"},{"name":"vasculitis, eosinophilic granulomatous","type":"exact"}],"termid":"MONDO:0015943","xrefs":{"Monarch":{"xref_id":"0015943"}}}


id: GO:0035202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of the tracheal pits, the first tube-like structures to form in the open tracheal system. Once cells are determined to their tracheal cell fate, the tracheal pits arise by invagination of each ectodermal cluster of tracheal placode cells, between 5 and 7 hours after egg laying. An example of this is found in Drosophila melanogaster.","definition_xrefs":["PMID:11992723","PMID:14570584","PMID:11063940","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"open tracheal system development","termid":"GO:0007424"}],"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":"tracheal pit formation in open tracheal system","synonyms":[{"name":"tracheal placode invagination","type":"related"},{"name":"tracheal sac formation","type":"broad"}],"termid":"GO:0035202"}


id: PBO:0117143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THUMP domain 2 tRNA and snRNA guanosine methyltransferase","termid":"PBO:0117143"}


id: PBO:0028226
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_alpha,alpha-trehalase_activity_during_cellular_response_to_heat","termid":"PBO:0028226"}


id: PBO:0043715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 6B1 pseudogene 3","termid":"PBO:0043715"}


id: MONDO:0000878
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection of the retina by cytomegalovirus characterized by retinal necrosis, hemorrhage, vessel sheathing, and retinal edema. Cytomegalovirus retinitis is a major opportunistic infection in aids patients and can cause blindness.","definition_xrefs":["MESH:D017726"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis","termid":"MONDO:0002708"},{"relation_name":"is_a","term_name":"cytomegalovirus infection","termid":"MONDO:0005132"},{"relation_name":"is_a","term_name":"endophthalmitis","termid":"MONDO:0016047"},{"relation_name":"is_a","term_name":"infectious disorder of the nervous system","termid":"MONDO:0020010"},{"relation_name":"is_a","term_name":"viral eye infection","termid":"MONDO:0020950"}],"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":"cytomegalovirus retinitis","secondary_identifiers":["GARD:9531","DOID:0080160","MEDGEN:61532","UMLS:C0206178","EFO:1001302","NCIT:C50521","SCTID:22455005"],"synonyms":[{"name":"CMV retinitis","type":"exact"},{"name":"Cytomegaloviral Retinitis","type":"exact"},{"name":"Cytomegalovirus caused retinitis","type":"exact"},{"name":"Cytomegalovirus retinitis","type":"exact"},{"name":"Retinitis, Cytomegaloviral","type":"exact"},{"name":"cytomegalovirus retinitis","type":"exact"}],"termid":"MONDO:0000878","xrefs":{"Monarch":{"xref_id":"0000878"}}}


id: GO:0002122
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Aggressive behavior associated with attempts to flee from a threat.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aggressive behavior","termid":"GO:0002118"}],"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":"fear-induced aggressive behavior","synonyms":[{"name":"fear-induced aggression","type":"exact"}],"termid":"GO:0002122"}


id: PBO:0052378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 21A","termid":"PBO:0052378"}


id: MONDO:0007657
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":"giant neutrophil leukocytes","secondary_identifiers":["OMIM:137500","UMLS:C1842039","MEDGEN:330754"],"synonyms":[{"name":"giant neutrophil leukocytes","type":"exact"}],"termid":"MONDO:0007657","xrefs":{"Monarch":{"xref_id":"0007657"}}}


id: PBO:0004337
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-consensus GC donor","termid":"PBO:0004337"}


id: PBO:0027283
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_nucleus,_with_protein_mislocalized_to_cytoplasm","termid":"PBO:0027283"}


id: PBO:0036485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arginine specific carbamoyl-phosphate synthase subunit Arg5","termid":"PBO:0036485"}


id: PBO:0046536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group 9 member 1","termid":"PBO:0046536"}


id: GO:0044739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism positively regulates the activity of a voltage-gated sodium channel in another organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of acid-sensing ion channel in another organism (obsolete GO:0044739)","synonyms":[{"name":"positive regulation of ASIC channel in other organism","type":"exact"},{"name":"positive regulation of acid-sensing ion channel in other organism","type":"exact"}],"termid":"GO:0044739"}


id: GO:2000698
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of epithelial cell differentiation involved in kidney development.","definition_xrefs":["GOC:yaf","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of epithelial cell differentiation","termid":"GO:0030858"},{"relation_name":"is_a","term_name":"regulation of epithelial cell differentiation involved in kidney development","termid":"GO:2000696"},{"relation_name":"positively_regulates","term_name":"epithelial cell differentiation involved in kidney development","termid":"GO:0035850"}],"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":"positive regulation of epithelial cell differentiation involved in kidney development","termid":"GO:2000698"}


id: GO:0061736
data:
  {"annotated_genes":["SJAG_05289"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110538],"is_not":false,"summary":null,"term":"GO:0061736"}]},"cv_name":"biological_process","definition":"The membrane invagination process by which an autophagosomal membrane surrounds an object that will be degraded by macroautophagy.","definition_xrefs":["GOC:pad","GOC:PARL","GOC:autophagy","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane invagination","termid":"GO:0010324"},{"relation_name":"part_of","term_name":"autophagosome assembly","termid":"GO:0000045"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0008150","GO:0061024","GO:0044085","GO:0006914"],"is_obsolete":false,"name":"engulfment of target by autophagosome","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061736","terms_by_termid":{"GO:0061736":null}}


id: MONDO:0017227
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Type 1 autoimmune pancreatitis is a form of autoimmune pancreatitis seen in elderly males (>60 years) and presenting with abdominal pain, steatorrhea, obstructive jaundice and other organ (bile duct, kidneys and retroperitoneum) involvement. It is thought to be due to an immunoglobulin G4 (IgG4)-associated systemic disease.","definition_xrefs":["Orphanet:280302"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic pancreatitis","termid":"MONDO:0005003"},{"relation_name":"is_a","term_name":"autoimmune pancreatitis","termid":"MONDO:0015175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"autoimmune pancreatitis type 1","secondary_identifiers":["EFO:1000780","UMLS:C4302243","PMID:25985088","GARD:21076","SCTID:722872000","MEDGEN:927912"],"synonyms":[{"name":"AIP type 1","type":"exact"},{"name":"IgG4-related pancreatitis","type":"exact"},{"name":"autoimmune pancreatitis type 1","type":"exact"},{"name":"lymphoplasmacytic sclerosing pancreatitis","type":"exact"}],"termid":"MONDO:0017227","xrefs":{"Monarch":{"xref_id":"0017227"}}}


id: GO:0000702
data:
  {"annotated_genes":["SJAG_02261","SJAG_01119","SJAG_03724"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034042"},{"annotations":[98099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034043"},{"annotations":[98100,75451,76184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034039"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of oxidized bases by cleaving the N-C1' glycosidic bond between the target damaged DNA base and the deoxyribose sugar. The reaction releases a free base and leaves an apurinic/apyrimidinic (AP) site.","definition_xrefs":["PMID:11554296","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA N-glycosylase activity","termid":"GO:0019104"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01119":null,"SJAG_02261":null,"SJAG_03724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0140097","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"oxidized base lesion DNA N-glycosylase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0000702","terms_by_termid":{"GO:0034039":null,"GO:0034042":null,"GO:0034043":null}}


id: PBO:0060139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial tRNA translation optimization 1","termid":"PBO:0060139"}


id: PBO:0089116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation elongation factor EF2 methyltransferase Efm3","termid":"PBO:0089116"}


id: GO:1990182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whereby a membrane-bounded vesicle is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane.","definition_xrefs":["PMID:10572093","PMID:12154376","GOC:hjd","PMID:18617898","PMID:16773132"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exocytosis","termid":"GO:0006887"},{"relation_name":"is_a","term_name":"establishment of vesicle localization","termid":"GO:0051650"},{"relation_name":"part_of","term_name":"extracellular exosome biogenesis","termid":"GO:0097734"}],"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":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0044085","GO:0051179","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"exosomal secretion","synonyms":[{"name":"exosomal protein secretion","type":"narrow"},{"name":"exosomal secretory pathway","type":"exact"},{"name":"extracellular vesicular exosome secretion","type":"exact"},{"name":"multi-vesicular body fusion with plasma membrane","type":"exact"},{"name":"secretion of exosome","type":"exact"}],"termid":"GO:1990182"}


id: PBO:0050061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLCS antisense RNA 1","termid":"PBO:0050061"}


id: FYPO:0000602
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the G1 phase of the mitotic cell cycle is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"},{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle phase","termid":"FYPO:0002736"}],"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:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000631","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal mitotic G1 phase progression","synonyms":[{"name":"abnormal G1 phase progression during mitotic cell cycle","type":"exact"},{"name":"abnormal mitotic G1 phase progression during vegetative growth","type":"exact"},{"name":"abnormal mitotic cell cycle progression in G1","type":"exact"},{"name":"mitotic cell cycle progression in G1 phase: abnormal","type":"related"}],"termid":"FYPO:0000602"}


id: PBO:0076765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tudor domain containing 3","termid":"PBO:0076765"}


id: GO:0075237
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of zoospore movement on or near its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of zoospore movement on or near host (obsolete GO:0075237)","termid":"GO:0075237"}


id: PR:Q92352
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An actin-related protein 2/3 complex subunit 4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["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":"actin-related protein 2/3 complex subunit 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6G9.07c","secondary_identifiers":["UniProtKB:Q92352"],"synonyms":[{"name":"SPAC6G9.07c","type":"related"},{"name":"Spom972h-ARPC4","type":"exact"},{"name":"arp2/3 complex 20 kDa (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"arp20","type":"related"},{"name":"p20-ARC (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q92352"}


id: PBO:0081569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 496","termid":"PBO:0081569"}


id: PATO:0000405
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's having parallel chains in undulate fashion on the border.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curled","termid":"PATO:0000405"}


id: GO:0102767
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-naringenin + S-adenosyl-L-methionine = 2 H+ + ponciretin + S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.231","GOC:pz"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016741","GO:0016740"],"is_obsolete":false,"name":"flavanone 4'-O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-12719","RHEA:31743"],"termid":"GO:0102767"}


id: GO:0033593
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex formed of BRCA2 and MAGE-D1; may mediate the synergistic activities of the two proteins in regulating cell growth.","definition_xrefs":["PMID:15930293"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"BRCA2-MAGE-D1 complex","termid":"GO:0033593"}


id: MONDO:0018343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial periodic paralysis","termid":"MONDO:0000995"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"hereditary neuromuscular disease","termid":"MONDO:0100546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"periodic paralysis with later-onset distal motor neuropathy","secondary_identifiers":["UMLS:C4751573","GARD:21634","MEDGEN:1670241","Orphanet:397750"],"termid":"MONDO:0018343","xrefs":{"Monarch":{"xref_id":"0018343"}}}


id: MONDO:0019140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute ackee fruit intoxication (also referred to as Jamaican vomiting syndrome or sickness) is caused by the ingestion of unripe Blighia sapida fruits. It is a serious intoxication that is frequent in certain countries in the Caribbean and Western Africa. In contrast, it is rare in France and other Western countries. Intoxication leads to toxic hypoglycaemia and inhibition of neoglucogenesis. The hypoglycaemia is caused by the effect of hypoglycin A, which is found in the arils.","definition_xrefs":["Orphanet:73423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute ackee fruit intoxication","secondary_identifiers":["MESH:C537562","ICD9:988.2","SCTID:49434001","GARD:9299"],"synonyms":[{"name":"Jamaican vomiting sickness","type":"exact"},{"name":"Jamaican vomiting syndrome","type":"exact"},{"name":"ackee poisoning","type":"related"},{"name":"acute intoxication by Blighia sapida","type":"exact"}],"termid":"MONDO:0019140","xrefs":{"Monarch":{"xref_id":"0019140"}}}


id: PBO:0013093
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Replication Uncoupled from Mitosis","termid":"PBO:0013093"}


id: PBO:0059958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 3","termid":"PBO:0059958"}


id: PBO:0004021
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mads BoX protein","termid":"PBO:0004021"}


id: MONDO:0007529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete acquired dermis elastic tissue disorder with increased elastic tissue (obsolete MONDO:0016436)","termid":"MONDO:0016436"},{"relation_name":"is_a","term_name":"dermis disorder","termid":"MONDO:0021154"}],"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":"elastosis perforans serpiginosa","secondary_identifiers":["GARD:10103","UMLS:C0221271","MedDRA:10014338","Orphanet:79148","MEDGEN:65137","ICD10CM:L87.2","OMIM:130100","icd11.foundation:1430012917","MESH:C536202","SCTID:49428008"],"synonyms":[{"name":"Miescher elastoma","type":"related"},{"name":"elastoma Intrapapillare perforans verruciformis","type":"related"},{"name":"elastosis perforans serpiginosa","type":"exact"},{"name":"eps","type":"related"}],"termid":"MONDO:0007529","xrefs":{"Monarch":{"xref_id":"0007529"}}}


id: PBO:0044798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin alpha 11, pseudogene","termid":"PBO:0044798"}


id: PBO:0003710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein Ymr1 (predicted)","termid":"PBO:0003710"}


id: GO:2000760
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of N-terminal peptidyl-lysine acetylation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein maturation","termid":"GO:1903318"},{"relation_name":"is_a","term_name":"negative regulation of peptidyl-lysine acetylation","termid":"GO:2000757"},{"relation_name":"is_a","term_name":"regulation of N-terminal peptidyl-lysine acetylation","termid":"GO:2000759"},{"relation_name":"negatively_regulates","term_name":"N-terminal peptidyl-lysine acetylation","termid":"GO:0018076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0051604"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0051604"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051604"],"is_obsolete":false,"name":"negative regulation of N-terminal peptidyl-lysine acetylation","termid":"GO:2000760"}


id: PBO:0059572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1X","termid":"PBO:0059572"}


id: SO:0000266
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A tRNA sequence that has a methionine anticodon, and a 3' methionine binding region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"methionine_tRNA_primary_transcript","termid":"SO:0000223"},{"relation_name":"is_a","term_name":"tRNA","termid":"SO:0000253"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methionyl_tRNA","synonyms":[{"name":"methionyl tRNA","type":"exact"},{"name":"methionyl-transfer RNA","type":"exact"},{"name":"methionyl-transfer ribonucleic acid","type":"exact"}],"termid":"SO:0000266"}


id: PBO:0080882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YPEL5 pseudogene 2","termid":"PBO:0080882"}


id: PBO:0050483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox A11","termid":"PBO:0050483"}


id: MONDO:0018191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tumor of testis and paratestis (obsolete MONDO:0018191)","secondary_identifiers":["Orphanet:363472"],"synonyms":[{"name":"testicular and paratesticular tumor","type":"exact"},{"name":"testicular and paratesticular tumour","type":"exact"}],"termid":"MONDO:0018191","xrefs":{"Monarch":{"xref_id":"0018191"}}}


id: GO:0102063
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate(3-) = diphosphoric acid + (-)-beta-curcumene.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete beta-curcumene synthase activity (obsolete GO:0102063)","termid":"GO:0102063"}


id: MONDO:0018975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A clinically heterogeneous, neurocutaneous genetic disorder characterized by cafe-au-lait spots, iris Lisch nodules, axillary and inguinal freckling, and multiple neurofibromas.","definition_xrefs":["Orphanet:636"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"excluded_subClassOf","term_name":"obsolete Moyamoya syndrome (obsolete MONDO:0018792)","termid":"MONDO:0018792"},{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"excluded_subClassOf","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"is_a","term_name":"RASopathy","termid":"MONDO:0021060"},{"relation_name":"is_a","term_name":"neurofibromatosis","termid":"MONDO:0021061"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"neurofibromatosis type 1","secondary_identifiers":["MESH:C538607","MESH:D009456","SCTID:92824003","MedDRA:10047712","DECIPHER:15","icd11.foundation:337970533","ICD10CM:Q85.01","NANDO:1200226","NANDO:2100287","NANDO:2201003","DOID:0111253","GARD:7866","NANDO:1200225","OMIM:162200","ICD9:237.71","MEDGEN:18013","NCIT:C3273","UMLS:C0027831","NORD:1502"],"synonyms":[{"name":"NF1","type":"exact"},{"name":"Neurofibromatosis 1","type":"exact"},{"name":"Nf1-Microdeletion syndrome","type":"exact"},{"name":"Recklinghausen's disease","type":"related"},{"name":"Von Recklinghausen disease","type":"related"},{"name":"neurofibromatosis","type":"broad"},{"name":"neurofibromatosis 1","type":"exact"},{"name":"neurofibromatosis type 1","type":"exact"},{"name":"neurofibromatosis type 1 microdeletion syndrome","type":"related"},{"name":"neurofibromatosis type i","type":"exact"},{"name":"neurofibromatosis, peripheral type","type":"related"},{"name":"neurofibromatosis, type 1","type":"exact"},{"name":"neurofibromatosis, type I","type":"related"},{"name":"nonmosaic NF1","type":"exact"},{"name":"nonmosaic neurofibromatosis type 1","type":"exact"},{"name":"peripheral neurofibromatosis","type":"exact"},{"name":"type 1 neurofibromatosis","type":"related"},{"name":"von Reklinghausen disease","type":"related"}],"termid":"MONDO:0018975","xrefs":{"Monarch":{"xref_id":"0018975"}}}


id: GO:0021787
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a branchiomotor neuron growth cone in the neural tube is directed to a specific target site in the neural tube in response to a repulsive chemical cue. Branchiomotor neurons are located in the hindbrain and innervate branchial arch-derived muscles that control jaw movements, facial expression, the larynx, and the pharynx.","definition_xrefs":["GOC:dgh","GOC:dph","GOC:jid","GOC:cls","PMID:14699587","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branchiomotor neuron axon guidance in neural tube","termid":"GO:0021786"},{"relation_name":"is_a","term_name":"chemorepulsion of branchiomotor axon","termid":"GO:0021793"}],"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":"chemorepulsion of branchiomotor neuron axon in neural tube","synonyms":[{"name":"negative chemotaxis of branchiomotor neuron axon in neural tube","type":"exact"}],"termid":"GO:0021787"}


id: FYPO:0001852
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 lower extent than normal when the cell is subject to iron ion starvation. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"decreased RNA level during cellular response to iron ion starvation","termid":"FYPO:0002042"},{"relation_name":"is_a","term_name":"decreased transcription during vegetative growth","termid":"FYPO:0000781"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000294","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased transcription during iron starvation","synonyms":[{"name":"decreased transcription during iron depletion","type":"exact"},{"name":"decreased transcription during iron deprivation","type":"exact"},{"name":"decreased transcription during iron ion starvation","type":"exact"},{"name":"decreased transcription during iron starvation during mitotic cell cycle","type":"related"},{"name":"decreased transcription during iron starvation during vegetative growth","type":"exact"},{"name":"reduced transcription during iron starvation","type":"exact"}],"termid":"FYPO:0001852"}


id: PBO:0016980
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"this is not NADH complex associated in yeast, which do not have the other 40 subunits that are present in that complex in mammals, see associated refs for more info on the human protein","termid":"PBO:0016980"}


id: PBO:0085376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"[PIN(+)] prion; an infectious protein conformation that is generally an ordered protein aggregate","termid":"PBO:0085376"}


id: GO:0097364
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a calcium ion by a channel that opens in response to a mechanical stress in the form of stretching, and contributing to the regulation of action potential.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11","PMID:21290758"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stretch-activated, monoatomic cation-selective, calcium channel activity","termid":"GO:0015275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"stretch-activated, monoatomic cation-selective, calcium channel activity involved in regulation of action potential","synonyms":[{"name":"stretch-activated, cation-selective, calcium channel activity involved in regulation of action potential","type":"broad"}],"termid":"GO:0097364"}


id: GO:0009085
data:
  {"annotated_genes":["SJAG_04688","SJAG_01955","SJAG_01574","SJAG_03312","SJAG_00502","SJAG_02388","SJAG_01630","SJAG_01061","SJAG_00869"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[66156,78555,65501,98314,72058,115447,78124,76921,79343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019878"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lysine, 2,6-diaminohexanoic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysine metabolic process","termid":"GO:0006553"},{"relation_name":"is_a","term_name":"aspartate family amino acid biosynthetic process","termid":"GO:0009067"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00502":null,"SJAG_00869":null,"SJAG_01061":null,"SJAG_01574":null,"SJAG_01630":null,"SJAG_01955":null,"SJAG_02388":null,"SJAG_03312":null,"SJAG_04688":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"lysine biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:LYSINE-SYN"],"synonyms":[{"name":"lysine anabolism","type":"exact"},{"name":"lysine biosynthesis","type":"exact"},{"name":"lysine formation","type":"exact"},{"name":"lysine synthesis","type":"exact"}],"termid":"GO:0009085","terms_by_termid":{"GO:0019878":null}}


id: PBO:0088810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein, LARP1 family Slr1","termid":"PBO:0088810"}


id: FYPO:0002072
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which a prospore has a nucleus in an abnormal location. The normal location is at the midpoint of the long axis of the cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized nucleus","termid":"FYPO:0002069"},{"relation_name":"output_of","term_name":"abnormal nucleus positioning in prospore","termid":"FYPO:0000942"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"mislocalized nucleus in prospore","synonyms":[{"name":"abnormal nucleus location in prospore","type":"exact"},{"name":"abnormal nucleus position in prospore","type":"exact"},{"name":"displaced nucleus in prospore","type":"exact"},{"name":"displaced nucleus prospore","type":"exact"},{"name":"mislocalised nucleus in prospore","type":"exact"},{"name":"mislocalized nucleus in forespore","type":"exact"},{"name":"mislocalized prospore nucleus","type":"exact"},{"name":"misplaced prospore nuclei","type":"exact"},{"name":"misplaced prospore nucleus","type":"exact"},{"name":"nuclear displacement in prospore","type":"exact"}],"termid":"FYPO:0002072"}


id: GO:0008693
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (3R)-3-hydroxydecanoyl-[acyl-carrier protein] = 2,3-decenoyl-[acyl-carrier protein] or 3,4-decenoyl-[acyl-carrier protein] + H2O.","definition_xrefs":["PMID:8910376"],"gene_count":0,"genotype_count":0,"name":"obsolete (3R)-3-hydroxydecanoyl-[acyl-carrier-protein] dehydratase activity (obsolete GO:0008693)","synonyms":[{"name":"(3R)-3-hydroxydecanoyl-acyl-carrier-protein hydro-lyase activity","type":"exact"},{"name":"3-hydroxydecanoyl-ACP dehydratase activity","type":"exact"},{"name":"3-hydroxydecanoyl-[acyl-carrier protein] dehydratase activity","type":"exact"},{"name":"3-hydroxydecanoyl-[acyl-carrier-protein] dehydratase activity","type":"exact"},{"name":"3-hydroxydecanoyl-acyl carrier protein dehydrase activity","type":"exact"},{"name":"3-hydroxydecanoyl-acyl carrier protein dehydratase activity","type":"exact"},{"name":"3-hydroxydecanoyl-acyl-carrier-protein dehydratase activity","type":"exact"},{"name":"beta-hydroxyacyl-ACP dehydrase activity","type":"exact"},{"name":"beta-hydroxyacyl-acyl carrier protein dehydratase activity","type":"exact"},{"name":"beta-hydroxydecanoate dehydrase activity","type":"exact"},{"name":"beta-hydroxydecanoyl thioester dehydrase activity","type":"exact"}],"termid":"GO:0008693"}


id: GO:0000182
data:
  {"annotated_genes":["SJAG_04766","SJAG_05253","SJAG_04527","SJAG_03354","SJAG_00247","SJAG_03905","SJAG_04855"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73980,76041,104131,104869],"is_not":false,"summary":null,"term":"GO:0000182"},{"annotations":[117026],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043110"},{"annotations":[104235],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110035"},{"annotations":[71700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001002"}]},"cv_name":"molecular_function","definition":"Binding to a DNA sequence encoding a ribosomal RNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sequence-specific double-stranded DNA binding","termid":"GO:1990837"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00247":null,"SJAG_03354":null,"SJAG_03905":null,"SJAG_04527":null,"SJAG_04766":null,"SJAG_04855":null,"SJAG_05253":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003677"],"is_obsolete":false,"name":"rDNA binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"ribosomal DNA binding","type":"exact"}],"termid":"GO:0000182","terms_by_termid":{"GO:0000182":null,"GO:0001002":null,"GO:0043110":null,"GO:0110035":null}}


id: GO:0006558
data:
  {"annotated_genes":["SJAG_03124","SJAG_03312"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79820,100292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009094"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving L-phenylalanine, the L-enantiomer of 2-amino-3-phenylpropanoic acid, i.e. (2S)-2-amino-3-phenylpropanoic acid.","definition_xrefs":["GOC:mah","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aromatic amino acid metabolic process","termid":"GO:0009072"},{"relation_name":"is_a","term_name":"L-amino acid metabolic process","termid":"GO:0170033"},{"relation_name":"is_a","term_name":"proteinogenic amino acid metabolic process","termid":"GO:0170039"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03124":null,"SJAG_03312":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"L-phenylalanine metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-8964208"],"synonyms":[{"name":"L-phenylalanine metabolism","type":"exact"},{"name":"phenylalanine metabolic process","type":"broad"},{"name":"phenylalanine metabolism","type":"broad"}],"termid":"GO:0006558","terms_by_termid":{"GO:0009094":null}}


id: MONDO:0700260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any type 1 interferonopathies in which the cause of the disease is a variation in the SAMHD1 gene. Individuals with variants in SAMHD1 can present with a variety of phenotypes, including Aicardi-Goutieres syndrome and chilblain lupus.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"type 1 interferonopathy","termid":"MONDO:0700264"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAMHD1-related type 1 interferonopathy","termid":"MONDO:0700260","xrefs":{"Monarch":{"xref_id":"0700260"}}}


id: PATO:0001823
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A wetness quality inhering in a bearer by virtue of the bearer's being covered by a liquid.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"wetness","termid":"PATO:0001822"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wet","termid":"PATO:0001823"}


id: PBO:0012845
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by H. sapiens SHFM1","termid":"PBO:0012845"}


id: GO:0010118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of opening or closing of stomata, which is directly related to the stomatal conductance (measuring rate of passage of either water vapor or carbon dioxide (CO2) through stomata).","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"}],"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":"stomatal movement","termid":"GO:0010118"}


id: MONDO:0013926
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the WDR11 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kallmann syndrome","termid":"MONDO:0018800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 14 with or without anosmia","secondary_identifiers":["ICD10CM:E23.0","OMIM:614858","DOID:0090087","GARD:15857","MEDGEN:761703","UMLS:C3540450"],"synonyms":[{"name":"HH14","type":"related"},{"name":"WDR11 hypogonadotropic hypogonadism","type":"exact"},{"name":"hypogonadotropic hypogonadism 14 with or without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism caused by mutation in WDR11","type":"exact"}],"termid":"MONDO:0013926","xrefs":{"Monarch":{"xref_id":"0013926"}}}


id: GO:0051945
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of catecholamine neurotransmitters into a neuron or glial cell.","definition_xrefs":["GOC:ai","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of neurotransmitter uptake","termid":"GO:0051581"},{"relation_name":"is_a","term_name":"regulation of catecholamine uptake involved in synaptic transmission","termid":"GO:0051940"},{"relation_name":"is_a","term_name":"negative regulation of amine transport","termid":"GO:0051953"},{"relation_name":"negatively_regulates","term_name":"catecholamine uptake involved in synaptic transmission","termid":"GO:0051934"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of catecholamine uptake involved in synaptic transmission","synonyms":[{"name":"down regulation of catecholamine uptake during transmission of nerve impulse","type":"exact"},{"name":"down-regulation of catecholamine uptake during transmission of nerve impulse","type":"exact"},{"name":"downregulation of catecholamine uptake during transmission of nerve impulse","type":"exact"},{"name":"inhibition of catecholamine uptake during transmission of nerve impulse","type":"narrow"},{"name":"negative regulation of catecholamine neurotransmitter reuptake","type":"exact"},{"name":"negative regulation of catecholamine neurotransmitter uptake","type":"exact"},{"name":"negative regulation of catecholamine uptake during transmission of nerve impulse","type":"broad"}],"termid":"GO:0051945"}


id: GO:1990348
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the removal of adenine misinserted into nascent strand opposite guanine in the template by adenine DNA glycosylase activity. The reaction leaves an apurinic AP site. I also requested same term but for Go/A mismatch. If you think it is better to make one term for mismatched adenine that is fine by me.","definition_xrefs":["PMID:9737967"],"gene_count":0,"genotype_count":0,"name":"obsolete G/A mismatch specific adenine DNA glycosylase activity (obsolete GO:1990348)","synonyms":[{"name":"G/A mismatch specific adenine DNA glycosylase activity","type":"exact"}],"termid":"GO:1990348"}


id: GO:0050445
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-sulfanyl-2-(sulfanylmethyl)propanoate + NAD+ = asparagusate + NADH + H+.","definition_xrefs":["RHEA:14881"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"asparagusate reductase (NADH) activity","secondary_identifiers":["EC:1.8.1.11","MetaCyc:ASPARAGUSATE-REDUCTASE-NADH-RXN","KEGG_REACTION:R03761"],"synonyms":[{"name":"3-mercapto-2-mercaptomethylpropanoate:NAD+ oxidoreductase activity","type":"related"},{"name":"NADH2:asparagusate oxidoreductase activity","type":"related"},{"name":"NADH:asparagusate oxidoreductase activity","type":"related"},{"name":"asparagusate dehydrogenase activity","type":"related"},{"name":"asparagusate reductase (NADH2)","type":"related"},{"name":"asparagusate reductase activity","type":"exact"},{"name":"asparagusic dehydrogenase activity","type":"related"}],"termid":"GO:0050445"}


id: FYPO:0003096
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 methylation of lysine at position 9 of histone H3 in centromere outer repeat regions occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000872"},{"relation_name":"is_a","term_name":"abnormal histone methylation at centromere during vegetative growth","termid":"FYPO:0007374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0002274","FYPO:0001985","FYPO:0001320","FYPO:0002494"],"is_obsolete":false,"name":"decreased histone H3-K9 methylation at centromere outer repeat during vegetative growth","synonyms":[{"name":"decreased histone H3 K9 methylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 methylation at centromere otr during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 methylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"decreased histone H3-K9 methylation at centromeric dg repeats during vegetative growth","type":"narrow"},{"name":"decreased histone H3-K9 methylation at centromeric outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 methylation at pericentric region during vegetative growth","type":"related"},{"name":"decreased histone H3-K9 methylation at pericentromeric region during vegetative growth","type":"related"},{"name":"decreased histone H3K9me at centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K9 methylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"reduced histone H3-K9 methylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0003096"}


id: PBO:0076265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI5 homologous recombination repair protein","termid":"PBO:0076265"}


id: PBO:0055676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIPE antisense RNA 1","termid":"PBO:0055676"}


id: PBO:0073697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spindle and kinetochore associated complex subunit 2 pseudogene 1","termid":"PBO:0073697"}


id: FYPO:0002118
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a specified transporter activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transmembrane transporter activity","termid":"FYPO:0002116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002114"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0002114","FYPO:0005447","FYPO:0000707"],"is_obsolete":false,"name":"decreased transporter activity","synonyms":[{"name":"reduced transporter activity","type":"exact"}],"termid":"FYPO:0002118"}


id: MONDO:0000132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypocalcemia (obsolete MONDO:0000132)","synonyms":[{"name":"obsolete hypocalcemia (disease)","type":"exact"}],"termid":"MONDO:0000132","xrefs":{"Monarch":{"xref_id":"0000132"}}}


id: GO:0008389
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: coumarin + O2 + NADPH + H+ = hydroxycoumarin + H2O + NADP+.","definition_xrefs":["PMID:2733794","PMID:10490589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"coumarin 7-hydroxylase activity","secondary_identifiers":["Reactome:R-HSA-76453","Reactome:R-HSA-211881"],"synonyms":[{"name":"cytochrome P450 CYP2A5","type":"narrow"}],"termid":"GO:0008389"}


id: MONDO:0003098
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurogenic tumor that arises from the mediastinum. Neural tumors are the most common tumors that arise from the posterior mediastinum. Representative examples include Schwannoma, neurofibroma, and neuroblastoma.","definition_xrefs":["NCIT:C6624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral nervous system neoplasm","termid":"MONDO:0001406"},{"relation_name":"is_a","term_name":"neoplasm of mediastinum","termid":"MONDO:0021386"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediastinal neural neoplasm","secondary_identifiers":["UMLS:C1334672","DOID:4691","MEDGEN:277353"],"synonyms":[{"name":"malignant mediastinal neurogenic neoplasm","type":"related"},{"name":"mediastinal neural neoplasm","type":"exact"},{"name":"mediastinal neural tumor","type":"exact"},{"name":"mediastinal neural tumour","type":"exact"},{"name":"mediastinal neurogenic neoplasm","type":"exact"},{"name":"mediastinal neurogenic tumor","type":"exact"},{"name":"mediastinal neurogenic tumour","type":"exact"},{"name":"neurogenic neoplasm of mediastinum","type":"exact"},{"name":"neurogenic neoplasm of the mediastinum","type":"exact"},{"name":"neurogenic tumor of mediastinum","type":"exact"},{"name":"neurogenic tumor of the mediastinum","type":"exact"},{"name":"neurogenic tumour of mediastinum","type":"exact"},{"name":"neurogenic tumour of the mediastinum","type":"exact"}],"termid":"MONDO:0003098","xrefs":{"Monarch":{"xref_id":"0003098"}}}


id: MONDO:0008195
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paramyotonia congenita of Von Eulenburg is characterized by exercise- or cold-induced myotonia and muscle weakness. Prevalence is unknown. The syndrome is nonprogressive and is transmitted as an autosomal dominant trait. It is caused by mutations in the gene encoding the alpha subunit of the type IV voltage-gated sodium channel (SCN4A; 17q23.3).","definition_xrefs":["Orphanet:684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myotonic syndrome","termid":"MONDO:0016120"},{"relation_name":"is_a","term_name":"hereditary skeletal muscle disorder","termid":"MONDO:0700223"},{"relation_name":"is_a","term_name":"SCN4A-related channelopathy","termid":"MONDO:0800468"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paramyotonia congenita of Von Eulenburg","secondary_identifiers":["icd11.foundation:1740060527","NCIT:C122790","OMIM:168300","SCTID:41574007","MEDGEN:113142","NANDO:1200501","UMLS:C0221055","DOID:0111538","GARD:7325","ICD9:359.29"],"synonyms":[{"name":"Eulenburg disease","type":"related"},{"name":"PMC","type":"related"},{"name":"Von Eulenburg paramyotonia congenita","type":"related"},{"name":"myotonia congenita intermittens","type":"related"},{"name":"paralysis periodica Paramyotonica","type":"related"},{"name":"paramyotonia congenita","type":"exact"},{"name":"paramyotonia congenita of VON Eulenburg","type":"related"},{"name":"paramyotonia congenita of Von Eulenburg","type":"exact"},{"name":"paramyotonia congenita without cold paralysis","type":"related"}],"termid":"MONDO:0008195","xrefs":{"Monarch":{"xref_id":"0008195"}}}


id: PBO:0050236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene14","termid":"PBO:0050236"}


id: GO:0102494
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A20 + O2 + a reduced electron acceptor = gibberellin A5 + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete GA20 2,3-desaturase activity (obsolete GO:0102494)","termid":"GO:0102494"}


id: FYPO:0007243
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell polarity phenotype in which the switch from the monopolar to bipolar mode of cell growth (new end take-off; NETO) is normal (i.e. indistinguishable from wild type) in one, and premature in the other, of the daughter cells formed as a result of the division of a mother cell in which NETO did not occurs. NETO is normal in the daughter cell that inherits the parent cell's old end, and begins earlier than normal in the daughter cell that inherits parent cell's new end. Normally, growth begins at the old end and then becomes bipolar with similar timing in both daughter cells.","definition_xrefs":["PMID:31719163","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal NETO in daughter cells","termid":"FYPO:0007240"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0005568"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0005568"],"is_obsolete":false,"name":"normal NETO in cell derived from growing end and premature NETO in cell derived from non-growing end","synonyms":[{"name":"normal NETO in cell derived from growing end and premature NETO in cell derived from non-growing end during mitotic cell cycle","type":"related"},{"name":"normal NETO in cell derived from growing end and premature NETO in cell derived from non-growing end during vegetative growth","type":"exact"},{"name":"normal activation of bipolar cell growth in cell derived from growing end and premature activation of bipolar cell growth in cell derived from non-growing end","type":"related"},{"name":"normal cell growth mode switching, monopolar to bipolar in cell derived from growing end and premature cell growth mode switching, monopolar to bipolar in cell derived from non-growing end","type":"exact"},{"name":"normal new end take-off in cell derived from growing end and premature NETO in cell derived from non-growing end","type":"exact"},{"name":"normal switch from monopolar to bipolar cell growth in cell derived from growing end and premature switch from monopolar to bipolar cell growth in cell derived from non-growing end","type":"exact"}],"termid":"FYPO:0007243"}


id: PBO:0051154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-33-2 (pseudogene)","termid":"PBO:0051154"}


id: MONDO:1011262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Non-progressive vision impairment in dim or absent lighting in dogs due to a variation in the LRIT3 gene.","definition_xrefs":["PMID:35316139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"congenital blindness, non-human animal","termid":"MONDO:1011975"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital stationary night blindness, LRIT3-related, dog","secondary_identifiers":["OMIA:001486-9615"],"termid":"MONDO:1011262","xrefs":{"Monarch":{"xref_id":"1011262"}}}


id: GO:0039703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cellular metabolic process in which a cell duplicates one or more molecules of RNA.","definition_xrefs":["GOC:jl","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA metabolic process","termid":"GO:0016070"}],"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 replication","termid":"GO:0039703"}


id: GO:0140248
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a ubiquitin molecule to histone 3 at the lysine-18 residue.","definition_xrefs":["PMID:27595565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 ubiquitin ligase activity","termid":"GO:0141055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0019787"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004842"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0019787","GO:0140096","GO:0016746","GO:0004842"],"is_obsolete":false,"name":"histone H3K18 ubiquitin ligase activity","termid":"GO:0140248"}


id: PBO:0091910
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHD Finger protein","termid":"PBO:0091910"}


id: MONDO:0000791
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A allergy involving a Cyprinus carpio.","definition_xrefs":["MONDO:patterns/allergy"],"gene_count":0,"genotype_count":0,"name":"obsolete carp allergy (obsolete MONDO:0000791)","secondary_identifiers":["DOID:0060516"],"synonyms":[{"name":"Cyprinus carpio allergic disease","type":"exact"},{"name":"Cyprinus carpio caused allergic disease","type":"exact"},{"name":"Cyprinus carpio fish allergy","type":"exact"},{"name":"allergy of Cyprinus carpio","type":"exact"}],"termid":"MONDO:0000791","xrefs":{"Monarch":{"xref_id":"0000791"}}}


id: SO:0000460
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Germline genomic DNA with the sequence for a V, D, C, or J portion of an immunoglobulin/T-cell receptor.","direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immune_system_gene_recombination_feature","termid":"SO:0000301"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vertebrate_immunoglobulin_T_cell_receptor_segment","synonyms":[{"name":"vertebrate immunoglobulin T cell receptor segment","type":"exact"},{"name":"vertebrate_immunoglobulin/T-cell receptor gene","type":"exact"}],"termid":"SO:0000460"}


id: PR:O13687
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- vma4 gene.","definition_xrefs":["UniProtKB:O13687","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":"V-type proton ATPase subunit E (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11E3.07","synonyms":[{"name":"Spom972h-vma4","type":"exact"},{"name":"V-ATPase subunit E (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"vacuolar proton pump subunit E (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13687"}


id: MONDO:0800386
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A poisoning that is caused by exposure to organophosphate.","definition_xrefs":["MONDO:patterns/patterns/poisoning"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"organophosphate poisoning","synonyms":[{"name":"insecticide poisoning","type":"exact"},{"name":"organophosphate exposure","type":"exact"}],"termid":"MONDO:0800386","xrefs":{"Monarch":{"xref_id":"0800386"}}}


id: PBO:0029882
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_dimethylation_at_silent_mating-type_cassette","termid":"PBO:0029882"}


id: MONDO:0034819
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A rare familial intestinal malformation characterized by failure of the rotation of the developing gastrointestinal tract around the superior mesenteric artery during embryonic development, resulting in a spectrum of abnormalities of intestinal position and fixation. Patients most typically present in the neonatal period with midgut volvulus, which can lead to short bowel syndrome or even death. Signs and symptoms include bilious vomiting, feeding intolerance, failure to thrive, constipation, bloody stools, or intermittent apnea. The condition may also manifest later in life with complications like kinking or hernias and a broad range of intestinal symptoms. It can be an isolated finding or occur in association with other anomalies.","definition_xrefs":["Orphanet:508410"],"gene_count":0,"genotype_count":0,"name":"obsolete familial intestinal malrotation (obsolete MONDO:0034819)","termid":"MONDO:0034819","xrefs":{"Monarch":{"xref_id":"0034819"}}}


id: GO:0004342
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucosamine 6-phosphate + H2O = beta-D-fructose 6-phosphate + NH4.","definition_xrefs":["RHEA:12172","EC:3.5.99.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016810","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"glucosamine-6-phosphate deaminase activity","secondary_identifiers":["KEGG_REACTION:R00765","MetaCyc:GLUCOSAMINE-6-P-DEAMIN-RXN","Reactome:R-HSA-6799604"],"synonyms":[{"name":"2-amino-2-deoxy-D-glucose-6-phosphate aminohydrolase (ketol isomerizing)","type":"related"},{"name":"GlcN6P deaminase activity","type":"related"},{"name":"aminodeoxyglucosephosphate isomerase activity","type":"related"},{"name":"glucosamine phosphate deaminase activity","type":"related"},{"name":"glucosamine-6-phosphate isomerase activity","type":"related"},{"name":"glucosaminephosphate isomerase","type":"broad"},{"name":"phosphoglucosamine isomerase activity","type":"related"},{"name":"phosphoglucosaminisomerase activity","type":"related"}],"termid":"GO:0004342"}


id: GO:0010626
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency or extent of the multiplication or reproduction of Schwann cells, resulting in the expansion of their population. Schwann cells are a type of glial cell in the peripheral nervous system.","definition_xrefs":["GOC:sl","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of Schwann cell proliferation","termid":"GO:0010624"},{"relation_name":"is_a","term_name":"negative regulation of glial cell proliferation","termid":"GO:0060253"},{"relation_name":"negatively_regulates","term_name":"Schwann cell proliferation","termid":"GO:0014010"}],"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 Schwann cell proliferation","termid":"GO:0010626"}


id: GO:0035072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process induced by ecdysone that directly activates salivary gland programmed cell death during salivary gland histolysis.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete ecdysone-mediated induction of salivary gland cell autophagic cell death (obsolete GO:0035072)","termid":"GO:0035072"}


id: GO:0034683
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An integrin complex that comprises one alphav subunit and one beta3 subunit.","definition_xrefs":["PMID:12297042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integrin complex","termid":"GO:0008305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"integrin alphav-beta3 complex","synonyms":[{"name":"ITGAV-ITGB3 complex","type":"narrow"},{"name":"alphav-beta3 integrin complex","type":"exact"}],"termid":"GO:0034683"}


id: PBO:0049566
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B histone pseudogene 2","termid":"PBO:0049566"}


id: PBO:0110384
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 3121","termid":"PBO:0110384"}


id: MONDO:1010466
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Patent ductus arteriosus that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"patent ductus arteriosus, non-human animal","termid":"MONDO:1010017"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"patent ductus arteriosus, domestic cat","secondary_identifiers":["OMIA:000779-9685"],"termid":"MONDO:1010466","xrefs":{"Monarch":{"xref_id":"1010466"}}}


id: MONDO:0019112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cancer associated retinopathy (CAR) is a paraneoplastic disease of the eye associated with the presence of extraocular malignancy and circulating autoantibodies against retinal proteins.","definition_xrefs":["Orphanet:71505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"},{"relation_name":"is_a","term_name":"paraneoplastic neurologic syndrome","termid":"MONDO:0018215"}],"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":"cancer-associated retinopathy","secondary_identifiers":["SCTID:404663008","icd11.foundation:1216073790","UMLS:C1321315","GARD:18912","ICD9:362.10","MESH:D059545","MEDGEN:729915"],"synonyms":[{"name":"CAR syndrome","type":"exact"},{"name":"paraneoplastic retinopathy","type":"exact"}],"termid":"MONDO:0019112","xrefs":{"Monarch":{"xref_id":"0019112"}}}


id: MONDO:0008440
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by variable spastic paraplegia, bilateral sensorineural deafness, intellectual deficit and progressive nephropathy.","definition_xrefs":["Orphanet:2820"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"autosomal dominant complex spastic paraplegia","termid":"MONDO:0015087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0000426"],"is_obsolete":false,"name":"spastic paraplegia-nephritis-deafness syndrome","secondary_identifiers":["UMLS:C1866853","MEDGEN:355816","OMIM:182690","GARD:2342","MESH:C537937"],"synonyms":[{"name":"Fitzsimmons Walson Mellor syndrome","type":"related"},{"name":"Fitzsimmons-Walson-Mellor syndrome","type":"exact"},{"name":"spastic paraplegia - nephritis - deafness","type":"related"},{"name":"spastic paraplegia, bilateral sensorineural deafness, intellectual retardation, and progressive nephropathy","type":"related"},{"name":"spastic paraplegia, sensorineural deafness, intellectual disability, and progressive nephropathy","type":"related"},{"name":"spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy","type":"related"}],"termid":"MONDO:0008440","xrefs":{"Monarch":{"xref_id":"0008440"}}}


id: PBO:0028051
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_spindle_pole_body_morphology_during_meiosis_II","termid":"PBO:0028051"}


id: PBO:0080992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 24","termid":"PBO:0080992"}


id: GO:1901625
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 ergosterol stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to sterol","termid":"GO:0036315"},{"relation_name":"is_a","term_name":"cellular response to alcohol","termid":"GO:0097306"}],"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 ergosterol","termid":"GO:1901625"}


id: PATO:0002101
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A cellular quality inhering in a bearer by virtue of having changed from one fully differentiated state into another.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular potency","termid":"PATO:0001397"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaplastic","synonyms":[{"name":"trans-differentiated","type":"related"}],"termid":"PATO:0002101"}


id: PBO:0112232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome-associated ubiquitin receptor, S. cerevisiae Rad23 homolog, Rhp23","termid":"PBO:0112232"}


id: PBO:0046385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endothelium and lymphocyte associated ASCH domain 2","termid":"PBO:0046385"}


id: PBO:0055238
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 2665","termid":"PBO:0055238"}


id: PBO:0001025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA export shuttling protein","termid":"PBO:0001025"}


id: FYPO:0004160
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the meiotic spindle is normal (i.e. indistinguishable from wild type) with respect to structure, composition, location, and orientation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal spindle","termid":"FYPO:0004568"}],"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:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal meiotic spindle","synonyms":[{"name":"normal spindle during meiosis","type":"exact"},{"name":"normal spindle during meiotic nuclear division","type":"exact"}],"termid":"FYPO:0004160"}


id: MONDO:0014918
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tall stature-intellectual disability-renal anomalies syndrome","secondary_identifiers":["UMLS:C4310715","GARD:17921","MEDGEN:934682","OMIM:617107","Orphanet:500095"],"synonyms":[{"name":"THAUVIN-robinet-Faivre syndrome","type":"related"},{"name":"TROFAS","type":"exact"},{"name":"Thauvin-robinet-Faivre syndrome","type":"exact"}],"termid":"MONDO:0014918","xrefs":{"Monarch":{"xref_id":"0014918"}}}


id: PBO:0083967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Global transcriptional regulator, component of SAGA, TREX-2 complexes; interacts with RNA polymerase II; involved in mRNA export coupled transcription activation and elongation; involved in post-transcriptional tethering of active genes to nuclear periphery and to non-nascent mRNP; plays role in negatively regulating telomere length through modulation of H2BK123 mono-ubiquitination and its interaction with nuclear pore complex","termid":"PBO:0083967"}


id: GO:0070679
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to inositol 1,4,5 trisphosphate.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"alcohol binding","termid":"GO:0043178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"inositol 1,4,5 trisphosphate binding","synonyms":[{"name":"IP3 binding","type":"exact"},{"name":"InsP3 binding","type":"exact"}],"termid":"GO:0070679"}


id: MONDO:0976128
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epilepsy, idiopathic generalized, susceptibility to, 19","secondary_identifiers":["OMIM:621064"],"termid":"MONDO:0976128","xrefs":{"Monarch":{"xref_id":"0976128"}}}


id: PBO:0074733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 91","termid":"PBO:0074733"}


id: PBO:0050636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSFY1 pseudogene 1","termid":"PBO:0050636"}


id: PBO:0058938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MISP family member 3","termid":"PBO:0058938"}


id: MONDO:0033014
data:
  {"annotated_genes":["SJAG_02488"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87441],"is_not":false,"summary":null,"term":"MONDO:0033014"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"erythrokeratodermia variabilis","termid":"MONDO:0017851"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02488":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"erythrokeratodermia variabilis et progressiva 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080250","MEDGEN:1372799","OMIM:617526","GARD:18590","UMLS:C4479620"],"synonyms":[{"name":"EKVP4","type":"related"},{"name":"erythrokeratodermia variabilis ET progressiva 4","type":"related"},{"name":"erythrokeratodermia variabilis et progressiva 4","type":"exact"}],"termid":"MONDO:0033014","terms_by_termid":{"MONDO:0033014":null},"xrefs":{"Monarch":{"xref_id":"0033014"}}}


id: PBO:0120922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC71A1 antisense RNA 1","termid":"PBO:0120922"}


id: GO:0030043
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The severing of actin filaments into numerous short fragments, usually mediated by actin severing proteins.","definition_xrefs":["ISBN:0815316194","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament depolymerization","termid":"GO:0030042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007010","GO:0030036","GO:0008150"],"is_obsolete":false,"name":"actin filament fragmentation","termid":"GO:0030043"}


id: MONDO:0015789
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-acquired combined pituitary hormone deficiencies without extra-pituitary malformations (obsolete MONDO:0015789)","secondary_identifiers":["ICD10CM:E23.0","Orphanet:178025"],"termid":"MONDO:0015789","xrefs":{"Monarch":{"xref_id":"0015789"}}}


id: GO:0009070
data:
  {"annotated_genes":["SJAG_01880","SJAG_00234","SJAG_04449","SJAG_02450","SJAG_00582","SJAG_03914","SJAG_03152","SJAG_00881","SJAG_02791","SJAG_01766","SJAG_02313","SJAG_04305","SJAG_02972"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112495],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019344"},{"annotations":[67866,78039,61202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006535"},{"annotations":[74011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006545"},{"annotations":[75223,73963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019264"},{"annotations":[73036,75494,117783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009090"},{"annotations":[112496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071269"},{"annotations":[81464,118909,61726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006564"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of amino acids of the serine family, comprising cysteine, glycine, homoserine, selenocysteine and serine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine family amino acid metabolic process","termid":"GO:0009069"},{"relation_name":"is_a","term_name":"alpha-amino acid biosynthetic process","termid":"GO:1901607"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00234":null,"SJAG_00582":null,"SJAG_00881":null,"SJAG_01766":null,"SJAG_01880":null,"SJAG_02313":null,"SJAG_02450":null,"SJAG_02791":null,"SJAG_02972":null,"SJAG_03152":null,"SJAG_03914":null,"SJAG_04305":null,"SJAG_04449":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"serine family amino acid biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"serine family amino acid anabolism","type":"exact"},{"name":"serine family amino acid biosynthesis","type":"exact"},{"name":"serine family amino acid formation","type":"exact"},{"name":"serine family amino acid synthesis","type":"exact"}],"termid":"GO:0009070","terms_by_termid":{"GO:0006535":null,"GO:0006545":null,"GO:0006564":null,"GO:0009090":null,"GO:0019264":null,"GO:0019344":null,"GO:0071269":null}}


id: PBO:0028309
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_RNA_level_during_cellular_response_to_methylglyoxal","termid":"PBO:0028309"}


id: PBO:0065417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit beta 4","termid":"PBO:0065417"}


id: GO:0072695
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of DNA recombination within the telomere.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA recombination","termid":"GO:0000018"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0006310","GO:0008150"],"is_obsolete":false,"name":"regulation of DNA recombination at telomere","synonyms":[{"name":"regulation of telomeric recombination","type":"exact"}],"termid":"GO:0072695"}


id: PBO:0053978
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 1290","termid":"PBO:0053978"}


id: GO:1990093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The negative regulation of the receptor clustering process in which N-methyl-D-aspartate (NMDA) receptors are localized to distinct domains in the cell membrane.","definition_xrefs":["PMID:18442977"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of N-methyl-D-aspartate receptor clustering (obsolete GO:1990093)","synonyms":[{"name":"negative regulation of N-methyl-D-aspartate receptor clustering","type":"exact"},{"name":"negative regulation of NMDA receptor clustering","type":"exact"}],"termid":"GO:1990093"}


id: RO:0002255
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of has developmental contribution from","direct_ancestors":[{"relation_name":"is_a","term_name":"developmentally_succeeded_by","termid":"RO:0002286"},{"relation_name":"is_a","term_name":"has_potential_to_developmentally_contribute_to","termid":"RO:0002385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmentally_contributes_to","termid":"RO:0002255"}


id: FYECO:0000317
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which urea was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ urea","synonyms":[{"name":"urea added","type":"exact"}],"termid":"FYECO:0000317"}


id: PBO:0108706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ski complex WD repeat subunit Ski8","termid":"PBO:0108706"}


id: PBO:0028979
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cell_population_growth_on_methionine_sulfur_source","termid":"PBO:0028979"}


id: GO:1904729
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of intestinal lipid absorption.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:18768481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intestinal absorption","termid":"GO:1904478"},{"relation_name":"regulates","term_name":"intestinal lipid absorption","termid":"GO:0098856"}],"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 intestinal lipid absorption","termid":"GO:1904729"}


id: PBO:0087221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scaffold protein responsible for phagophore assembly site organization; regulatory subunit of an autophagy-specific complex that includes Atg1p and Atg13p; stimulates Atg1p kinase activity; human ortholog RB1CC1/FIP200 interacts with p53, which inhibits autophagy in human cells","termid":"PBO:0087221"}


id: PBO:0079881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uroplakin 2","termid":"PBO:0079881"}


id: GO:0010440
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an unspecialized epidermal cell progresses through a series of divisions that culminate in the production of a stomatal complex.","definition_xrefs":["GOC:expert_db","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"},{"relation_name":"part_of","term_name":"stomatal complex development","termid":"GO:0010374"}],"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":"stomatal lineage progression","termid":"GO:0010440"}


id: FYPO:0007685
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell growth phenotype in which vegetative cell population growth is increased relative to normal under conditions of starvation for one or more nutrients.","definition_xrefs":["PomBase:mah","PMID:33574613"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002057","FYPO:0002058","FYPO:0000139","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"increased vegetative cell population growth during nutrient starvation","synonyms":[{"name":"fast vegetative cell population growth during nutrient starvation","type":"narrow"},{"name":"increased vegetative cell population growth during nutrient depletion","type":"exact"},{"name":"increased vegetative cell population growth during nutrient deprivation","type":"exact"},{"name":"increased vegetative cell population growth during nutrient limitation","type":"exact"},{"name":"increased vegetative cell population growth in response to nutrient starvation","type":"exact"},{"name":"resistant to nutrient starvation","type":"related"}],"termid":"FYPO:0007685"}


id: PBO:0090282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ndc80 complex subunit Spc25","termid":"PBO:0090282"}


id: PBO:0116814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endoregulin","termid":"PBO:0116814"}


id: PBO:0046841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid binding protein 5 pseudogene 14","termid":"PBO:0046841"}


id: PBO:0113475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of tRNA-specific adenosine-34 deaminase; forms a heterodimer with Tad2p that converts adenosine to inosine at the wobble position of several tRNAs; localizes to cytosol, nucleus and peroxisomes","termid":"PBO:0113475"}


id: PBO:0049618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 21","termid":"PBO:0049618"}


id: MONDO:0015115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic metabolic liver disease (obsolete MONDO:0015115)","secondary_identifiers":["Orphanet:101940","MedDRA:10019689"],"termid":"MONDO:0015115","xrefs":{"Monarch":{"xref_id":"0015115"}}}


id: PR:O14029
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A microtubule-associated protein 1A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02252"],"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":"COPII coat assembly protein sec16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29B12.07","secondary_identifiers":["UniProtKB:O14029"],"synonyms":[{"name":"Spom972h-MAP1A","type":"exact"},{"name":"protein transport protein sec16 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14029"}


id: PBO:0040010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor like GTPase 17B","termid":"PBO:0040010"}


id: MONDO:0017262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A inherited ichthyosis that is not part of a larger syndrome.","definition_xrefs":["MONDO:patterns/isolated"],"gene_count":0,"genotype_count":0,"name":"obsolete inherited non-syndromic ichthyosis (obsolete MONDO:0017262)","secondary_identifiers":["Orphanet:281082","icd11.foundation:213831678"],"synonyms":[{"name":"isolated inherited ichthyosis","type":"exact"},{"name":"nonsyndromic inherited ichthyosis","type":"exact"}],"termid":"MONDO:0017262","xrefs":{"Monarch":{"xref_id":"0017262"}}}


id: PATO:0000817
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000817 anosmia (obsolete PATO:0000817)","termid":"PATO:0000817"}


id: MONDO:0001464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the sigmoid colon.","direct_ancestors":[{"relation_name":"is_a","term_name":"sigmoid neoplasm","termid":"MONDO:0006971"},{"relation_name":"is_a","term_name":"malignant colon neoplasm","termid":"MONDO:0021063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"sigmoid colon cancer","secondary_identifiers":["MEDGEN:509292","SCTID:363410008","UMLS:C0153436","ICD9:153.3","DOID:12192","ICD10CM:C18.7"],"synonyms":[{"name":"Ca sigmoid colon","type":"exact"},{"name":"cancer of sigmoid colon","type":"exact"},{"name":"malignant neoplasm of sigmoid colon","type":"exact"},{"name":"malignant sigmoid colon neoplasm","type":"exact"},{"name":"malignant tumor of sigmoid colon","type":"exact"},{"name":"malignant tumour of sigmoid colon","type":"exact"},{"name":"sigmoid colon cancer","type":"exact"}],"termid":"MONDO:0001464","xrefs":{"Monarch":{"xref_id":"0001464"}}}


id: GO:1900948
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of isoprene biosynthetic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid biosynthetic process","termid":"GO:0051055"},{"relation_name":"is_a","term_name":"negative regulation of olefin biosynthetic process","termid":"GO:1900912"},{"relation_name":"is_a","term_name":"negative regulation of isoprene metabolic process","termid":"GO:1900945"},{"relation_name":"is_a","term_name":"regulation of isoprene biosynthetic process","termid":"GO:1900947"},{"relation_name":"negatively_regulates","term_name":"isoprene biosynthetic process","termid":"GO:0043612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of isoprene biosynthetic process","synonyms":[{"name":"down regulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"down regulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"down regulation of hemiterpene biosynthesis","type":"exact"},{"name":"down regulation of hemiterpene biosynthetic process","type":"exact"},{"name":"down regulation of isoprene biosynthetic process","type":"exact"},{"name":"down-regulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"down-regulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"down-regulation of hemiterpene biosynthesis","type":"exact"},{"name":"down-regulation of hemiterpene biosynthetic process","type":"exact"},{"name":"down-regulation of isoprene biosynthetic process","type":"exact"},{"name":"downregulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"downregulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"downregulation of hemiterpene biosynthesis","type":"exact"},{"name":"downregulation of hemiterpene biosynthetic process","type":"exact"},{"name":"downregulation of isoprene biosynthetic process","type":"exact"},{"name":"inhibition of 2-methyl-1,3-butadiene biosynthesis","type":"narrow"},{"name":"inhibition of 2-methyl-1,3-butadiene biosynthetic process","type":"narrow"},{"name":"inhibition of hemiterpene biosynthesis","type":"narrow"},{"name":"inhibition of hemiterpene biosynthetic process","type":"narrow"},{"name":"inhibition of isoprene biosynthetic process","type":"narrow"},{"name":"negative regulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"negative regulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"negative regulation of hemiterpene biosynthesis","type":"exact"},{"name":"negative regulation of hemiterpene biosynthetic process","type":"exact"}],"termid":"GO:1900948"}


id: MOD:01875
data:
  {"annotated_genes":["SJAG_03641","SJAG_00464"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[82591],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00126"},{"annotations":[82660],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00127"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an N6-amino hydrogen atom of L-lysine with an acyl group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acylated residue","termid":"MOD:00670"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00464":null,"SJAG_03641":null},"genotype_count":0,"is_obsolete":false,"name":"N6-acylated L-lysine","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"N6AcylLys","type":"exact"}],"termid":"MOD:01875","terms_by_termid":{"MOD:00126":null,"MOD:00127":null}}


id: GO:0140647
data:
  {"annotated_genes":["SJAG_04397"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71132],"is_not":false,"summary":null,"term":"GO:0140647"}]},"cv_name":"biological_process","definition":"A electron transport chain in which one or more electron carriers operate to transfer electrons from donors to a cytochrome P450 protein or domain. Electron carriers operating in this chain include FAD-containing flavoproteins or domains, FMN domains, ferredoxins and cytochrome b5. The reduced cytochrome P450 functions as the terminal oxidase and participates in a wide range of biochemical pathways.","definition_xrefs":["PMID:16042601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"electron transport chain","termid":"GO:0022900"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04397":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"P450-containing electron transport chain","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["Wikipedia:P450-containing_systems"],"synonyms":[{"name":"P450-containing system","type":"related"}],"termid":"GO:0140647","terms_by_termid":{"GO:0140647":null}}


id: PBO:0066739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 36","termid":"PBO:0066739"}


id: FYPO:0007192
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 rapid, back-and-forth movement of the mitotic spindle pole body (SPB), and associated chromosome movement, do not occur. Normally, SPB oscillation occurs during mitotic interphase (as well as prophase) but is restricted to a small space.","definition_xrefs":["PMID:31483748","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body-led chromosome movement during mitotic interphase","termid":"FYPO:0005348"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abolished spindle pole body-led chromosome movement during mitotic interphase","synonyms":[{"name":"abolished mitotic SPB oscillation during mitotic interphase","type":"exact"},{"name":"abolished mitotic spindle pole body movement during mitotic interphase","type":"exact"},{"name":"abolished mitotic spindle pole body oscillation during mitotic interphase","type":"exact"},{"name":"abolished spindle pole body-led chromosome movement during interphase of mitotic cell cycle","type":"related"},{"name":"abolished spindle pole body-led chromosome movement during mitotic interphase during vegetative growth","type":"exact"},{"name":"mitotic spindle pole body oscillation abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0007192"}


id: PBO:0030744
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_phosphatidylinositol-3-phosphate_level","termid":"PBO:0030744"}


id: PBO:0077116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIMM23B-AGAP6 readthrough (NMD candidate)","termid":"PBO:0077116"}


id: MONDO:0054862
data:
  {"annotated_genes":["SJAG_02294","SJAG_02690"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88333,88334],"is_not":false,"summary":null,"term":"MONDO:0054862"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bone marrow disorder","termid":"MONDO:0003225"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02294":null,"SJAG_02690":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0005047"],"is_obsolete":false,"name":"premature ovarian failure 15","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080872","MEDGEN:1648369","UMLS:C4748170","OMIM:618096"],"synonyms":[{"name":"POF15","type":"related"},{"name":"premature ovarian failure 15","type":"exact"}],"termid":"MONDO:0054862","terms_by_termid":{"MONDO:0054862":null},"xrefs":{"Monarch":{"xref_id":"0054862"}}}


id: PBO:0089595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H2A-H2B chaperone, FACT complex subunit Spt16","termid":"PBO:0089595"}


id: MONDO:0022607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Brenner tumor that involves the vagina.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal neoplasm","termid":"MONDO:0021050"},{"relation_name":"is_a","term_name":"Brenner tumor","termid":"MONDO:0024235"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extraovarian Brenner tumor of the vagina","synonyms":[{"name":"Brenner tumor of the vagina","type":"related"},{"name":"Brenner tumour of the vagina","type":"related"},{"name":"extraovarian Brenner tumor of the vagina","type":"exact"},{"name":"vagina Brenner tumor","type":"exact"},{"name":"vagina Brenner tumour","type":"exact"}],"termid":"MONDO:0022607","xrefs":{"Monarch":{"xref_id":"0022607"}}}


id: PBO:0113496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translation elongation factor eIF-5A; required for translation of proteins containing polyproline stretches; structural homolog of bacterial EF-P; undergoes an essential hypusination modification; HYP2 has paralog ANB1 that arose from whole genome duplication; in humans EIF5A variants cause a disorder characterized by variable combinations of developmental delay, microcephaly, micrognathia and dysmorphism; human EIF5A complements inviability of yeast hyp2 anb1 double null mutant","termid":"PBO:0113496"}


id: PBO:0027402
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_protein_phosphorylation_during_cellular_response_to_oxidative_stress","termid":"PBO:0027402"}


id: GO:0070573
data:
  {"annotated_genes":["SJAG_01542","SJAG_04858"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[61180,62157],"is_not":false,"summary":null,"term":"GO:0070573"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a dipeptide by a mechanism in which water acts as a nucleophile, one or two metal ions hold the water molecule in place, and charged amino acid side chains are ligands for the metal ions.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metalloexopeptidase activity","termid":"GO:0008235"},{"relation_name":"is_a","term_name":"dipeptidase activity","termid":"GO:0016805"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01542":null,"SJAG_04858":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0008233","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"metallodipeptidase activity","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["Reactome:R-HSA-2022405","Reactome:R-HSA-2022398","Reactome:R-HSA-2065355"],"synonyms":[{"name":"metallo-exo-dipeptidase activity","type":"exact"},{"name":"metalloexodipeptidase activity","type":"exact"}],"termid":"GO:0070573","terms_by_termid":{"GO:0070573":null}}


id: GO:0015792
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which arabitol is transported across a lipid bilayer, from one side of a membrane to the other. Arabitol is the pentitol derived from arabinose or lyxose by reduction of the aldehyde group. The D enantiomer is present in lichens and mushrooms.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyol transmembrane transport","termid":"GO:0015791"},{"relation_name":"is_a","term_name":"carbohydrate transmembrane transport","termid":"GO:0034219"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"arabinitol transmembrane transport","synonyms":[{"name":"arabinitol transport","type":"related"},{"name":"arabitol transport","type":"related"}],"termid":"GO:0015792"}


id: FYPO:0002304
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 RNA measured in a cell during a cellular response to salt stress is lower than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during cellular response to osmotic stress","termid":"FYPO:0002286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased RNA level during cellular response to salt stress","synonyms":[{"name":"decreased RNA level during cellular response to salt stress during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to salt stress during vegetative growth","type":"exact"},{"name":"decreased mRNA level during cellular response to salt stress","type":"narrow"},{"name":"decreased transcript level during cellular response to salt stress","type":"exact"},{"name":"reduced RNA level during cellular response to salt stress","type":"exact"}],"termid":"FYPO:0002304"}


id: GO:0036043
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A dynamic, actin-rich projection extending from the surface of a migrating animal cell.","definition_xrefs":["PMID:19095735","PMID:12153987","PMID:11429692"],"gene_count":0,"genotype_count":0,"name":"obsolete microspike (obsolete GO:0036043)","synonyms":[{"name":"microspike","type":"exact"}],"termid":"GO:0036043"}


id: PBO:0089167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MutL family protein Mlh1","termid":"PBO:0089167"}


id: GO:1990779
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transmembrane signaling receptor complex found exclusively on platelets. Involved in haemostasis and thrombosis where it aids blood coagulation.","definition_xrefs":["PMID:1730602","PMID:25297919","GOC:bhm","PMID:23336709"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoprotein complex","termid":"GO:0090665"},{"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:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"glycoprotein Ib-IX-V complex","synonyms":[{"name":"CD42","type":"exact"},{"name":"GPIb-IX-V complex","type":"exact"},{"name":"GPIb-V-IX complex","type":"exact"}],"termid":"GO:1990779"}


id: GO:0005125
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The activity of a soluble extracellular gene product that interacts with a receptor to effect a change in the activity of the receptor to control the survival, growth, differentiation and effector function of tissues and cells.","definition_xrefs":["PMID:11530802","ISBN:0198599471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor ligand activity","termid":"GO:0048018"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140677","GO:0005515","GO:0005488","GO:0003674","GO:0098772"],"is_obsolete":false,"name":"cytokine activity","synonyms":[{"name":"autocrine activity","type":"related"},{"name":"paracrine activity","type":"related"},{"name":"phytocytokine activity","type":"narrow"}],"termid":"GO:0005125"}


id: MONDO:0011643
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete permanent neonatal diabetes mellitus (obsolete MONDO:0011643)","termid":"MONDO:0011643","xrefs":{"Monarch":{"xref_id":"0011643"}}}


id: MONDO:0008810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial hyperlipidemia","termid":"MONDO:0001336"},{"relation_name":"is_a","term_name":"syndromic dyslipidemia","termid":"MONDO:0015905"},{"relation_name":"is_a","term_name":"familial chylomicronemia syndrome","termid":"MONDO:0018637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"familial apolipoprotein C-II deficiency","secondary_identifiers":["Orphanet:309020","icd11.foundation:877401371","UMLS:C1720779","MEDGEN:328375","OMIM:207750","GARD:759","DOID:0111418","SCTID:33513003"],"synonyms":[{"name":"Apoc2 deficiency","type":"related"},{"name":"C-II Anapolipoproteinemia","type":"related"},{"name":"apolipoprotein C-II deficiency","type":"related"},{"name":"familial apoC-II deficiency","type":"exact"},{"name":"familial apolipoprotein C-II deficiency","type":"exact"},{"name":"hyperlipoproteinemia, type 1B","type":"related"},{"name":"hyperlipoproteinemia, type IB","type":"exact"}],"termid":"MONDO:0008810","xrefs":{"Monarch":{"xref_id":"0008810"}}}


id: PBO:0089848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"blue light photoreceptor Wcs1","termid":"PBO:0089848"}


id: GO:0062014
data:
  {"annotated_genes":["SJAG_05314","SJAG_03130","SJAG_02380","SJAG_01187","SJAG_00685","SJAG_04422","SJAG_02104"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95831],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"},{"annotations":[72740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045717"},{"annotations":[74975,78030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"},{"annotations":[113365,117481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"},{"annotations":[120009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905707"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of a small molecule metabolic process.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of metabolic process","termid":"GO:0009892"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"negatively_regulates","term_name":"small molecule metabolic process","termid":"GO:0044281"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_01187":null,"SJAG_02104":null,"SJAG_02380":null,"SJAG_03130":null,"SJAG_04422":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"negative regulation of small molecule metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"negative regulation of small molecule metabolism","type":"exact"}],"termid":"GO:0062014","terms_by_termid":{"GO:0010895":null,"GO:0045717":null,"GO:0045820":null,"GO:1905707":null,"GO:2001211":null}}


id: GO:0075200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of symbiont haustorium neck formation for entry into host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of symbiont haustorium neck formation for entry into host (obsolete GO:0075200)","termid":"GO:0075200"}


id: GO:0004035
data:
  {"annotated_genes":["SJAG_03108","SJAG_02853"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74053,77657],"is_not":false,"summary":null,"term":"GO:0004035"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a phosphate monoester + H2O = an alcohol + phosphate, with an alkaline pH optimum.","definition_xrefs":["EC:3.1.3.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02853":null,"SJAG_03108":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016788","GO:0016787"],"is_obsolete":false,"name":"alkaline phosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:ALKAPHOSPHA-RXN","Reactome:R-HSA-8878787"],"synonyms":[{"name":"alkaline phenyl phosphatase activity","type":"related"},{"name":"alkaline phosphohydrolase activity","type":"related"},{"name":"alkaline phosphomonoesterase activity","type":"related"},{"name":"glycerophosphatase activity","type":"broad"},{"name":"orthophosphoric-monoester phosphohydrolase (alkaline optimum)","type":"related"},{"name":"phosphate-monoester phosphohydrolase (alkaline optimum)","type":"related"},{"name":"phosphomonoesterase activity","type":"broad"}],"termid":"GO:0004035","terms_by_termid":{"GO:0004035":null}}


id: FYPO:0006064
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 septin ring disassembly is abnormal.","definition_xrefs":["PMID:15385632","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cytoskeleton organization during vegetative growth","termid":"FYPO:0001328"},{"relation_name":"is_a","term_name":"abnormal cellular component assembly during vegetative growth","termid":"FYPO:0001354"}],"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:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal septin ring disassembly during vegetative growth","synonyms":[{"name":"abnormal septin ring disassembly during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006064"}


id: GO:0060704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized structural and/or functional features that characterize an acinar cell of the salivary gland. Acinar cells are protein-secreting cells in the gland.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell differentiation involved in salivary gland development","termid":"GO:0060690"},{"relation_name":"is_a","term_name":"acinar cell differentiation","termid":"GO:0090425"}],"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":"acinar cell differentiation involved in salivary gland development","termid":"GO:0060704"}


id: _global:results_in_transport_to_from_or_in
data:
  {"annotation_feature_type":"gene","cv_name":"external","direct_ancestors":[{"relation_name":"is_a","term_name":"related_via_localization_to","termid":"_global:related_via_localization_to"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_transport_to_from_or_in","secondary_identifiers":["RO:0002344"],"termid":"_global:results_in_transport_to_from_or_in"}


id: PBO:0043580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type XII alpha 1 chain","termid":"PBO:0043580"}


id: PBO:0030445
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_separation_after_cytokinesis","termid":"PBO:0030445"}


id: MONDO:0019754
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multicentric castleman disease (MCD) is an aggressive form of Castleman disease that mostly results from human herpesvirus 8 (HHV8) infection. It manifests by fever, diffuse lymphadenopathy, hepatosplenomegaly, Involvement of the respiratory system and increased C-reactive protein.","definition_xrefs":["Orphanet:93686"],"direct_ancestors":[{"relation_name":"is_a","term_name":"human herpesvirus 8-related tumor","termid":"MONDO:0015157"},{"relation_name":"is_a","term_name":"Castleman disease","termid":"MONDO:0015564"}],"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":"multicentric Castleman disease","secondary_identifiers":["NCIT:C27855","MEDGEN:233197","GARD:22310","DOID:0111152","icd11.foundation:1590444463","Orphanet:570438","UMLS:C1334815"],"synonyms":[{"name":"HHV-8-associated multicentric Castleman disease","type":"exact"},{"name":"Human herpesvirus-8-associated multicentric Castleman disease","type":"exact"},{"name":"MCD","type":"exact"},{"name":"PMCD","type":"exact"},{"name":"idiopathic multicentric Castleman's disease","type":"related"},{"name":"multicentric Angiofollicular lymphoid hyperplasia","type":"exact"},{"name":"multicentric Castleman's disease","type":"exact"},{"name":"multicentric giant lymph node hyperplasia","type":"exact"},{"name":"multicentric plasma cell variant of Castleman's disease","type":"related"},{"name":"plasmablastic multicentric Castleman disease","type":"exact"}],"termid":"MONDO:0019754","xrefs":{"Monarch":{"xref_id":"0019754"}}}


id: MONDO:0012101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"juvenile open angle glaucoma","termid":"MONDO:0020367"}],"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":"glaucoma 1, open angle, J","secondary_identifiers":["MEDGEN:324818","GARD:18228","MESH:C563874","OMIM:608695","UMLS:C1837528"],"synonyms":[{"name":"GLC1J","type":"exact"},{"name":"JOAG1J","type":"exact"},{"name":"JOAG2","type":"exact"},{"name":"glaucoma 1, open angle, J","type":"exact"},{"name":"glaucoma, primary open angle, juvenile-onset, 2","type":"related"}],"termid":"MONDO:0012101","xrefs":{"Monarch":{"xref_id":"0012101"}}}


id: PBO:0084574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Membrane protein of unknown function; overexpression suppresses NaCl sensitivity of sro7 mutant cells by restoring sodium pump (Ena1p) localization to the plasma membrane","termid":"PBO:0084574"}


id: GO:0060110
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The layer of cuticle most closely apposed to the hypodermal cells. The morphology of the basal layer varies with life stage. In adult C. elegans animals, the basal layers is comprised of three sublayers: two fibrous layers whose fibers run in clockwise and counter-clockwise directions meeting one another at a 60 degree angle, and an amorphous basal layer that lies underneath the fibrous layers and directly contacts the hypodermis. In C. elegans dauer and L1 larval stage animals, the basal layer is characterized by a striated pattern that appears to derive from interwoven laminae. An example of this component is found in Caenorhabditis elegans.","definition_xrefs":["ISSN:15518507","GOC:dph","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cuticular extracellular matrix","termid":"GO:0060102"}],"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":"basal layer of collagen and cuticulin-based cuticle extracellular matrix","synonyms":[{"name":"basal layer of collagen and cuticulin-based exoskeleton extracellular matrix","type":"related"}],"termid":"GO:0060110"}


id: PBO:0066547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of G protein signaling 10","termid":"PBO:0066547"}


id: PBO:0068675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 56, pseudogene","termid":"PBO:0068675"}


id: PBO:0036048
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-curved_mitotic_spindle_during_anaphase_B","termid":"PBO:0036048"}


id: GO:0098795
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A posttranscriptional gene silencing pathway that involves the cleavage of mRNAs in a non-gene-specific manner.","definition_xrefs":["PMID:15009896"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-transcriptional gene silencing","termid":"GO:0016441"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_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":"global gene silencing by mRNA cleavage","secondary_identifiers":["GO:0030423"],"synonyms":[{"name":"RNA interference, targeting of mRNA for destruction","type":"related"},{"name":"gene silencing by mRNA cleavage","type":"broad"},{"name":"mRNA cleavage involved in gene silencing","type":"broad"},{"name":"mRNA destabilization-mediated gene silencing","type":"related"},{"name":"targeting of mRNA for destruction involved in RNA interference","type":"related"}],"termid":"GO:0098795"}


id: GO:1905908
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of amyloid fibril formation.","definition_xrefs":["GOC:aruk","GOC:TermGenie","GOC:bc","PMID:23106396","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein metabolic process","termid":"GO:0051247"},{"relation_name":"is_a","term_name":"positive regulation of supramolecular fiber organization","termid":"GO:1902905"},{"relation_name":"is_a","term_name":"regulation of amyloid fibril formation","termid":"GO:1905906"},{"relation_name":"positively_regulates","term_name":"amyloid fibril formation","termid":"GO:1990000"}],"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":"positive regulation of amyloid fibril formation","synonyms":[{"name":"activation of amyloid fibril assembly","type":"related"},{"name":"activation of amyloid fibril formation","type":"narrow"},{"name":"activation of amyloid structure assembly","type":"related"},{"name":"activation of amyloid structure formation","type":"related"},{"name":"positive regulation of amyloid fibril assembly","type":"related"},{"name":"positive regulation of amyloid structure assembly","type":"related"},{"name":"positive regulation of amyloid structure formation","type":"related"},{"name":"up regulation of amyloid fibril assembly","type":"related"},{"name":"up regulation of amyloid fibril formation","type":"exact"},{"name":"up regulation of amyloid structure assembly","type":"related"},{"name":"up regulation of amyloid structure formation","type":"related"},{"name":"up-regulation of amyloid fibril assembly","type":"related"},{"name":"up-regulation of amyloid fibril formation","type":"exact"},{"name":"up-regulation of amyloid structure assembly","type":"related"},{"name":"up-regulation of amyloid structure formation","type":"related"},{"name":"upregulation of amyloid fibril assembly","type":"related"},{"name":"upregulation of amyloid fibril formation","type":"exact"},{"name":"upregulation of amyloid structure assembly","type":"related"},{"name":"upregulation of amyloid structure formation","type":"related"}],"termid":"GO:1905908"}


id: MONDO:0010264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A X-linked condition characterized by underdevelopment of the adrenal gland and adrenal insufficiency caused by mutation(s) in the NR0B1 gene, resulting in decreased activity of the nuclear receptor protein DAX1, which may be associated with hypogonadotropic hypogonadism.","definition_xrefs":["NCIT:C123725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"chronic primary adrenal insufficiency","termid":"MONDO:0015129"},{"relation_name":"is_a","term_name":"congenital hypogonadotropic hypogonadism","termid":"MONDO:0015770"},{"relation_name":"is_a","term_name":"alternating hemiplegia of childhood","termid":"MONDO:0016241"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0700092"],"is_obsolete":false,"name":"X-linked adrenal hypoplasia congenita","secondary_identifiers":["NANDO:2200357","NANDO:1200403","DOID:0080156","Orphanet:95702","OMIM:300200","SCTID:93235007","UMLS:C0342482","GARD:555","MEDGEN:87442"],"synonyms":[{"name":"AHC","type":"broad"},{"name":"AHC with HHG","type":"related"},{"name":"AHC with isolated gonadotropin deficiency","type":"related"},{"name":"Addison disease, X-linked","type":"related"},{"name":"X-linked AHC","type":"related"},{"name":"X-linked adrenal hypoplasia congenita","type":"exact"},{"name":"X-linked congenital adrenal hypoplasia","type":"exact"},{"name":"adrenal hypoplasia congenita","type":"broad"},{"name":"adrenal hypoplasia, congenital","type":"related"},{"name":"adrenal hypoplasia, congenital, X-linked recessive","type":"exact"},{"name":"adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism","type":"related"},{"name":"adrenal hypoplasia, congenital, with precocious puberty","type":"related"},{"name":"adrenal insufficiency, progressive, and hypogonadotropic hypogonadism","type":"related"},{"name":"congenital adrenal hypoplasia","type":"exact"},{"name":"cytomegalic adrenocortical hypoplasia","type":"related"},{"name":"cytomegalic congenital adrenal hypoplasia","type":"related"},{"name":"mineralocorticoid deficiency, isolated","type":"related"}],"termid":"MONDO:0010264","xrefs":{"Monarch":{"xref_id":"0010264"}}}


id: SO:0002293
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The non-coding region of the mitochondrial genome that controls RNA and DNA synthesis.","definition_xrefs":["PMID:10968878"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"mitochondrial_sequence","termid":"SO:0000737"},{"relation_name":"is_a","term_name":"origin_of_replication","termid":"SO:0000296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial_control_region","secondary_identifiers":["https://en.wikipedia.org/wiki/MtDNA_control_region"],"synonyms":[{"name":"Mitochondrial A+T region","type":"exact"},{"name":"Mitochondrial DNA control region","type":"exact"},{"name":"Mitochondrial NCR","type":"exact"},{"name":"Mitochondrial noncoding region","type":"exact"},{"name":"MtDNA control region","type":"exact"},{"name":"MtDNA_control_region","type":"exact"}],"termid":"SO:0002293"}


id: GO:0072019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the proximal convoluted tubule over time, from its formation to the mature structure. The proximal convoluted tubule is the most proximal portion of the proximal tubule and extends from the glomerular capsule to the proximal straight tubule.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron tubule development","termid":"GO:0072080"},{"relation_name":"part_of","term_name":"proximal tubule development","termid":"GO:0072014"}],"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":"proximal convoluted tubule development","termid":"GO:0072019"}


id: FYPO:0001782
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 nucleus is constricted in the middle, resembling a figure 8.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear morphology during vegetative growth","termid":"FYPO:0000062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002403","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"constricted nucleus","synonyms":[{"name":"constricted nuclei","type":"exact"},{"name":"constricted nucleus during mitotic cell cycle","type":"related"},{"name":"constricted nucleus during vegetative growth","type":"exact"}],"termid":"FYPO:0001782"}


id: PBO:0083469
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 verified gene PET130","termid":"PBO:0083469"}


id: PBO:0088823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab GAP Gyp3","termid":"PBO:0088823"}


id: GO:0086033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled acetylcholine receptor signaling pathway that contributes to a decrease in frequency or rate of heart contraction. Binding of acetylcholine to a G protein-coupled (muscarinic) receptor on the surface of the signal-receiving cell results in the alpha subunit of a coupled G-protein binding to GTP. This results in the separation of the beta-gamma complex from the alpha subunit. Both the alpha subunit, and the beta-gamma complex can continue to signal to bring about membrane hyperpolarization and a reduction in heart rate.","definition_xrefs":["Wikipedia:G_protein-gated_ion_channel","GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled acetylcholine receptor signaling pathway involved in heart process","termid":"GO:0086093"},{"relation_name":"part_of","term_name":"negative regulation of heart rate by acetylcholine","termid":"GO:0003063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"G protein-coupled acetylcholine receptor signaling pathway involved in negative regulation of heart rate","synonyms":[{"name":"G-protein coupled acetylcholine receptor signaling pathway involved in negative regulation of heart rate","type":"exact"},{"name":"M2 receptor signalling pathway involved in negative regulation of heart rate","type":"exact"},{"name":"muscarinic acetylcholine receptor signaling pathway involved in negative regulation of heart rate","type":"exact"},{"name":"muscarinic receptor signalling pathway involved in negative regulation of heart rate","type":"exact"}],"termid":"GO:0086033"}


id: PR:Q10300
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC22H10.06c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10300"],"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 C22H10.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22H10.06c","synonyms":[{"name":"Spom972h-SPAC22H10.06c","type":"exact"}],"termid":"PR:Q10300"}


id: PBO:0051893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit alpha 2b","termid":"PBO:0051893"}


id: PBO:0116410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S. pombe specific DUF999 family protein 6","termid":"PBO:0116410"}


id: GO:0042100
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of a B cell population by cell division. Follows B cell activation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell activation","termid":"GO:0042113"},{"relation_name":"is_a","term_name":"lymphocyte proliferation","termid":"GO:0046651"}],"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":"B cell proliferation","secondary_identifiers":["GO:0042114"],"synonyms":[{"name":"B lymphocyte proliferation","type":"exact"},{"name":"B-cell proliferation","type":"exact"},{"name":"B-lymphocyte proliferation","type":"exact"}],"termid":"GO:0042100"}


id: MONDO:0008895
data:
  {"annotated_genes":["SJAG_02580","SJAG_02959","SJAG_02582"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88859,88860,88861],"is_not":false,"summary":null,"term":"MONDO:0008895"}]},"cv_name":"mondo","definition":"Hereditary arterial and articular multiple calcification syndrome is a very rare genetic vascular disease of autosomal recessive inheritance, described in less than 20 patients to date, characterized by adult-onset (as early as the second decade of life) isolated calcification of the arteries of the lower extremities (including the iliac, femoral, and tibial arteries) as well as the capsule joints of the fingers, wrists, ankles and feet, and that usually manifests with mild paresthesias of the lower extremities, intense joint pain and swelling, and early onset arthritis of affected joints.","definition_xrefs":["Orphanet:289601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02580":null,"SJAG_02582":null,"SJAG_02959":null},"genotype_count":0,"is_obsolete":false,"name":"hereditary arterial and articular multiple calcification syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:211800","DOID:0111582","SCTID:718602007","UMLS:C1859372","MESH:C565891","GARD:10762","MEDGEN:347132"],"synonyms":[{"name":"ACDC","type":"related"},{"name":"CALJA","type":"exact"},{"name":"arterial calcification and distal joint calcification","type":"related"},{"name":"arterial calcification due to CD73 deficiency","type":"related"},{"name":"arterial calcification due to deficiency of Cd73","type":"related"},{"name":"calcification of joints and arteries","type":"exact"}],"termid":"MONDO:0008895","terms_by_termid":{"MONDO:0008895":null},"xrefs":{"Monarch":{"xref_id":"0008895"}}}


id: FYPO:0003034
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 RNA measured in a cell during a cellular response to ultraviolet light is lower than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0006551"],"is_obsolete":false,"name":"decreased RNA level during cellular response to UV","synonyms":[{"name":"decreased RNA accumulation during cellular response to ultraviolet light","type":"related"},{"name":"decreased RNA level during cellular response to UV during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to UV during vegetative growth","type":"exact"},{"name":"decreased RNA level during cellular response to ultraviolet light","type":"exact"},{"name":"decreased transcript level during cellular response to UV","type":"exact"},{"name":"reduced RNA level during cellular response to UV","type":"exact"}],"termid":"FYPO:0003034"}


id: GO:0042584
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a chromaffin granule, a specialized secretory vesicle found in the cells of adrenal glands and various other organs, which is concerned with the synthesis, storage, metabolism, and secretion of epinephrine and norepinephrine.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule membrane","termid":"GO:0030667"},{"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:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"chromaffin granule membrane","termid":"GO:0042584"}


id: GO:1901848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of nicotinate.","definition_xrefs":["GOC:yaf","GOC:TermGenie","UniPathway:UPA00830"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkaloid catabolic process","termid":"GO:0009822"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"},{"relation_name":"is_a","term_name":"pyridine-containing compound catabolic process","termid":"GO:0072526"},{"relation_name":"is_a","term_name":"nicotinate metabolic process","termid":"GO:1901847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"nicotinate catabolic process","synonyms":[{"name":"nicotinate breakdown","type":"exact"},{"name":"nicotinate catabolism","type":"exact"},{"name":"nicotinate degradation","type":"exact"}],"termid":"GO:1901848"}


id: PATO:0001354
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A optical quality inhering in a bearer by virtue of the bearer's exhibiting low opacity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opacity","termid":"PATO:0000957"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translucent","termid":"PATO:0001354"}


id: PBO:0108915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STAG3 cohesin complex component like 1 (pseudogene)","termid":"PBO:0108915"}


id: MONDO:0700344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any ciliopathy caused by variants in the CEP164 gene. This disease is characterized by a broad range of phenotypes including various combinations of nephronophthisis, respiratory system impact, retinal degeneration, developmental delay, CNS malformations, polydactyly, bronchiectasis and obesity.","definition_xrefs":["PMID:27708425","PMID:34132027","PMID:22863007","PMID:36273371","MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliopathy","termid":"MONDO:0005308"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"CEP164-related ciliopathy","synonyms":[{"name":"ciliopathy-CEP164","type":"exact"}],"termid":"MONDO:0700344","xrefs":{"Monarch":{"xref_id":"0700344"}}}


id: MONDO:0008920
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":"carnitine deficiency, myopathic","secondary_identifiers":["OMIM:212160","MESH:C536100","MEDGEN:347852","UMLS:C1859318"],"synonyms":[{"name":"carnitine deficiency, myopathic","type":"exact"},{"name":"myopathic carnitine deficiency","type":"related"}],"termid":"MONDO:0008920","xrefs":{"Monarch":{"xref_id":"0008920"}}}


id: MONDO:0002508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder involving inflammation of the gums; may affect surrounding and supporting structures of the teeth.","definition_xrefs":["NCIT:C34636"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gingival disorder","termid":"MONDO:0002021"},{"relation_name":"is_a","term_name":"stomatitis","termid":"MONDO:0004842"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gingivitis","secondary_identifiers":["ICD9:523.10","MESH:D005891","DOID:3087","ICD9:523.0","SCTID:66383009","ICD9:523.1","MEDGEN:4895","UMLS:C0017574"],"synonyms":[{"name":"acute gingivitis","type":"narrow"},{"name":"chronic gingivitis","type":"narrow"},{"name":"gingiva inflammation","type":"exact"},{"name":"gingivitis","type":"exact"},{"name":"inflammation of gingiva","type":"exact"}],"termid":"MONDO:0002508","xrefs":{"Monarch":{"xref_id":"0002508"}}}


id: PBO:0089378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate dehydrogenase e1 component alpha subunit Pda1","termid":"PBO:0089378"}


id: GO:0051477
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a mannosylglycerate from one side of a membrane to the other.","definition_xrefs":["GOC:ai","PMID:15034926"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transmembrane transporter activity","termid":"GO:0015144"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"},{"relation_name":"is_a","term_name":"carbohydrate derivative transmembrane transporter activity","termid":"GO:1901505"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"mannosylglycerate transmembrane transporter activity","termid":"GO:0051477"}


id: PBO:0077175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"talin 2","termid":"PBO:0077175"}


id: PBO:0053130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LCT antisense RNA 1","termid":"PBO:0053130"}


id: PATO:0001248
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of cyan hue and low brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyan","termid":"PATO:0000319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dark cyan","termid":"PATO:0001248"}


id: GO:0035091
data:
  {"annotated_genes":["SJAG_00115","SJAG_00368","SJAG_00216","SJAG_02468","SJAG_03756","SJAG_01324","SJAG_00971","SJAG_01135","SJAG_01309","SJAG_04221","SJAG_02613","SJAG_01769","SJAG_03705","SJAG_03250","SJAG_03405","SJAG_01945","SJAG_04024","SJAG_00118","SJAG_02248","SJAG_02492","SJAG_04275","SJAG_00970","SJAG_01564","SJAG_03721","SJAG_02657","SJAG_04077","SJAG_04010","SJAG_04960","SJAG_04963","SJAG_05179","SJAG_04644","SJAG_00638","SJAG_03170","SJAG_02392","SJAG_02728","SJAG_01519","SJAG_01143","SJAG_01748","SJAG_02166","SJAG_01382","SJAG_03851","SJAG_00173","SJAG_05245","SJAG_01783","SJAG_04219","SJAG_00821","SJAG_00314","SJAG_02852","SJAG_00907","SJAG_01722","SJAG_01516","SJAG_02587","SJAG_00663","SJAG_02572","SJAG_00152","SJAG_02989","SJAG_01794","SJAG_02912","SJAG_00117","SJAG_00053"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62103,62125,63722,67956,69327,69332,70078,74134,75870,77915,79221,80328,92360,99405,100932,106336,109601,114858,118241],"is_not":false,"summary":null,"term":"GO:0035091"},{"annotations":[75516,110184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005545"},{"annotations":[97809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901981"},{"annotations":[119466,104377,90006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005547"},{"annotations":[75288,73715,79636,81744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080025"},{"annotations":[101795,72390,74992,81741,76486,106795,111621,69059,73712,80191,82188,93454,101794,92525,111978,97883,75285,101656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032266"},{"annotations":[119537,64065,75517,74481,119042,101241,116883,103727,92694,108568,120998,89938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005546"},{"annotations":[101242,114494,79472,102082,119913,96458,104378],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070273"}]},"cv_name":"molecular_function","definition":"Binding to an inositol-containing glycerophospholipid, i.e. phosphatidylinositol (PtdIns) and its phosphorylated derivatives.","definition_xrefs":["ISBN:0198506732","PMID:11395417","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid binding","termid":"GO:0005543"}],"gene_count":60,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00115":null,"SJAG_00117":null,"SJAG_00118":null,"SJAG_00152":null,"SJAG_00173":null,"SJAG_00216":null,"SJAG_00314":null,"SJAG_00368":null,"SJAG_00638":null,"SJAG_00663":null,"SJAG_00821":null,"SJAG_00907":null,"SJAG_00970":null,"SJAG_00971":null,"SJAG_01135":null,"SJAG_01143":null,"SJAG_01309":null,"SJAG_01324":null,"SJAG_01382":null,"SJAG_01516":null,"SJAG_01519":null,"SJAG_01564":null,"SJAG_01722":null,"SJAG_01748":null,"SJAG_01769":null,"SJAG_01783":null,"SJAG_01794":null,"SJAG_01945":null,"SJAG_02166":null,"SJAG_02248":null,"SJAG_02392":null,"SJAG_02468":null,"SJAG_02492":null,"SJAG_02572":null,"SJAG_02587":null,"SJAG_02613":null,"SJAG_02657":null,"SJAG_02728":null,"SJAG_02852":null,"SJAG_02912":null,"SJAG_02989":null,"SJAG_03170":null,"SJAG_03250":null,"SJAG_03405":null,"SJAG_03705":null,"SJAG_03721":null,"SJAG_03756":null,"SJAG_03851":null,"SJAG_04010":null,"SJAG_04024":null,"SJAG_04077":null,"SJAG_04219":null,"SJAG_04221":null,"SJAG_04275":null,"SJAG_04644":null,"SJAG_04960":null,"SJAG_04963":null,"SJAG_05179":null,"SJAG_05245":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0008289"],"is_obsolete":false,"name":"phosphatidylinositol binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"phosphoinositide binding","type":"exact"}],"termid":"GO:0035091","terms_by_termid":{"GO:0005545":null,"GO:0005546":null,"GO:0005547":null,"GO:0032266":null,"GO:0035091":null,"GO:0070273":null,"GO:0080025":null,"GO:1901981":null}}


id: GO:0071333
data:
  {"annotated_genes":["SJAG_01754","SJAG_04026","SJAG_04312","SJAG_01254","SJAG_00574","SJAG_02444","SJAG_03081","SJAG_01699","SJAG_00472"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118562,103805,96174,107869,110992,108466,117532,108816,111502],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010619"}]},"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 a glucose stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular glucose homeostasis","termid":"GO:0001678"},{"relation_name":"is_a","term_name":"response to glucose","termid":"GO:0009749"},{"relation_name":"is_a","term_name":"cellular response to hexose stimulus","termid":"GO:0071331"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00472":null,"SJAG_00574":null,"SJAG_01254":null,"SJAG_01699":null,"SJAG_01754":null,"SJAG_02444":null,"SJAG_03081":null,"SJAG_04026":null,"SJAG_04312":null},"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 glucose stimulus","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0071333","terms_by_termid":{"GO:0010619":null}}


id: PBO:0078806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 23-1","termid":"PBO:0078806"}


id: GO:2000280
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of root development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"root development","termid":"GO:0048364"}],"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 root development","termid":"GO:2000280"}


id: CHEBI:52646
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"A leptomycin having a (2E,10E,12E,16Z,18E)-double bond configuration as well as an ethyl substituent at position 17.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leptomycin B","termid":"CHEBI:52646"}


id: MONDO:0011612
data:
  {"annotated_genes":["SJAG_02901","SJAG_03861"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958179"},{"annotations":[88319],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958192"}]},"cv_name":"mondo","definition":"Glycine encephalopathy (GE) is an inborn error of glycine metabolism characterized by accumulation of glycine in body fluids and tissues, including the brain, resulting in neurometabolic symptoms of variable severity.","definition_xrefs":["Orphanet:407"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"inborn disorder of serine family metabolism","termid":"MONDO:0019239"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02901":null,"SJAG_03861":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"glycine encephalopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1491869639","OMIMPS:605899","MEDGEN:155625","DOID:9268","GARD:7219","ICD9:270.7","NANDO:1200984","NANDO:2200476","NCIT:C84937","NORD:1512","SCTID:237939006","UMLS:C0751748"],"synonyms":[{"name":"GCE","type":"related"},{"name":"GLYCINE encephalopathy","type":"related"},{"name":"Glycine synthase deficiency","type":"related"},{"name":"NKA","type":"exact"},{"name":"Nonketotic Hyperglycinemia","type":"exact"},{"name":"glycine encephalopathy","type":"exact"},{"name":"hyperglycinemia nonketotic","type":"related"},{"name":"hyperglycinemia, Nonketotic","type":"related"},{"name":"hyperglycinemia, transient neonatal","type":"related"},{"name":"non-ketotic hyperglycinemia","type":"exact"},{"name":"nonketotic hyperglycinemia","type":"exact"}],"termid":"MONDO:0011612","terms_by_termid":{"MONDO:0958179":null,"MONDO:0958192":null},"xrefs":{"Monarch":{"xref_id":"0011612"}}}


id: PBO:0052857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 4-17, pseudogene","termid":"PBO:0052857"}


id: PBO:0069199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 453, pseudogene","termid":"PBO:0069199"}


id: GO:0048932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of compact myelin sheaths around the axons of the posterior lateral line nerve.","definition_xrefs":["PMID:12112375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myelination of lateral line nerve axons","termid":"GO:0048897"},{"relation_name":"part_of","term_name":"posterior lateral line nerve glial cell morphogenesis involved in differentiation","termid":"GO:0048942"}],"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":"myelination of posterior lateral line nerve axons","termid":"GO:0048932"}


id: PBO:0068626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 6, pseudogene","termid":"PBO:0068626"}


id: GO:0015982
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of coupled solute translocation in which two solutes equilibrate across an osmotic barrier, the translocation of solute being coupled to the translocation of the other in the opposite direction.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete antiport (obsolete GO:0015982)","synonyms":[{"name":"antiport","type":"exact"}],"termid":"GO:0015982"}


id: MONDO:0000784
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A fruit allergy triggered by Cucumis melo plant fruit food product.","definition_xrefs":["DOID:0060509"],"gene_count":0,"genotype_count":0,"name":"obsolete melon allergy (obsolete MONDO:0000784)","synonyms":[{"name":"Cucumis melo fruit allergy","type":"exact"}],"termid":"MONDO:0000784","xrefs":{"Monarch":{"xref_id":"0000784"}}}


id: SO:0002279
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The hAT terminal inverted repeat transposon superfamily elements were first found in maize (the Ac/Ds elements). Members of the hAT superfamily have TSDs of 8 bp, relatively short TIRs of 5–27 bp and overall lengths of less than 4 kb.","definition_xrefs":["PMID:11454746"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hAT_TIR_transposon","synonyms":[{"name":"Ac transposon","type":"exact"},{"name":"Ac/Ds transposon","type":"exact"},{"name":"DTA transposon","type":"exact"},{"name":"Ds transposon","type":"exact"},{"name":"hAT TIR transposon","type":"exact"},{"name":"hAT transposon","type":"exact"},{"name":"hAT-Ac transposon","type":"exact"}],"termid":"SO:0002279"}


id: FYPO:0006788
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of poly(A)-specific ribonuclease activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased ribonuclease activity","termid":"FYPO:0003822"},{"relation_name":"is_a","term_name":"abnormal poly(A)-specific ribonuclease activity","termid":"FYPO:0006787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000654","FYPO:0000652","FYPO:0001985","FYPO:0000661"],"is_obsolete":false,"name":"decreased poly(A)-specific ribonuclease activity","synonyms":[{"name":"reduced poly(A)-specific ribonuclease activity","type":"exact"}],"termid":"FYPO:0006788"}


id: PBO:0087205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-adenosylmethionine-dependent lysine methyltransferase; involved in the trimethylation of eEF1A (Tef1p/Tef2p) at lysine 79; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; required for replication of Brome mosaic virus in budding yeast; expresses a circular RNA; originally misclassified as a N-6-adenine specific DNA methyltransferase based on sequence similarity; both Efm5p and human ortholog N6AMT2 can methylate eEF1a from either species in vitro","termid":"PBO:0087205"}


id: GO:0033363
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 secretory granule. A secretory granule is a small subcellular vesicle, surrounded by a membrane, that is formed from the Golgi apparatus and contains a highly concentrated protein destined for secretion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle organization","termid":"GO:0016050"},{"relation_name":"part_of","term_name":"endomembrane system organization","termid":"GO:0010256"}],"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":"secretory granule organization","synonyms":[{"name":"secretory granule organisation","type":"exact"},{"name":"secretory granule organization and biogenesis","type":"related"}],"termid":"GO:0033363"}


id: GO:0008341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A change in state or activity of a mature individual as the result of a cocaine stimulus. As in, but not restricted to, the true insects (Insecta, ncbi_taxonomy_id:50557).","definition_xrefs":["GOC:jid","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete response to cocaine (sensu Insecta) (obsolete GO:0008341)","synonyms":[{"name":"response to cocaine (sensu Insecta)","type":"exact"}],"termid":"GO:0008341"}


id: PBO:0002979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purine transporter (predicted)","termid":"PBO:0002979"}


id: PBO:0088792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA replication termination factor Rtf2","termid":"PBO:0088792"}


id: FYPO:0007983
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed during mitotic interphase in which some microtubule bundles are not anchored to the nuclear membrane. See PMID:15068790","definition_xrefs":["PMID:15068790","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule bundle","termid":"FYPO:0005558"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002399"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0002399","FYPO:0000002","FYPO:0000054"],"is_obsolete":false,"name":"microtubule bundles detached from the nuclear envelope","termid":"FYPO:0007983"}


id: PBO:0027118
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_zygotic_meiosis_II","termid":"PBO:0027118"}


id: MONDO:0013746
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any ventricular septal defect in which the cause of the disease is a mutation in the GATA4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ventricular septal defect","termid":"MONDO:0002070"},{"relation_name":"is_a","term_name":"structural congenital heart disease, multiple types - GATA4","termid":"MONDO:0100009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"ventricular septal defect 1","secondary_identifiers":["MEDGEN:482407","OMIM:614429","UMLS:C3280777"],"synonyms":[{"name":"GATA4 ventricular septal defect (disease)","type":"exact"},{"name":"VSD1","type":"related"},{"name":"ventricular septal defect (disease) caused by mutation in GATA4","type":"exact"},{"name":"ventricular septal defect 1","type":"exact"},{"name":"ventricular septal defect type 1","type":"exact"}],"termid":"MONDO:0013746","xrefs":{"Monarch":{"xref_id":"0013746"}}}


id: PBO:0061699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUPR2 pseudogene 1","termid":"PBO:0061699"}


id: GO:0004713
data:
  {"annotated_genes":["SJAG_01181","SJAG_00996","SJAG_04280","SJAG_03854","SJAG_00718","SJAG_00402","SJAG_02104","SJAG_04980","SJAG_04457"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72578,73085,80471,91604,94114,95839,104893,112175,112975],"is_not":false,"summary":null,"term":"GO:0004713"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + a protein tyrosine = ADP + protein tyrosine phosphate.","definition_xrefs":["RHEA:10596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase activity","termid":"GO:0004672"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00402":null,"SJAG_00718":null,"SJAG_00996":null,"SJAG_01181":null,"SJAG_02104":null,"SJAG_03854":null,"SJAG_04280":null,"SJAG_04457":null,"SJAG_04980":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0016740","GO:0004672","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"protein tyrosine kinase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9026579","Reactome:R-HSA-5654587","Reactome:R-HSA-1470009","Reactome:R-HSA-9032532","GO:0004718","Reactome:R-HSA-373750","Reactome:R-HSA-391866","Reactome:R-HSA-1982066","Reactome:R-HSA-8848776","Reactome:R-HSA-873919","Reactome:R-HSA-372693","Reactome:R-HSA-388831","Reactome:R-HSA-9666425","Reactome:R-HSA-1963582","Reactome:R-HSA-9700175","Reactome:R-HSA-879925","Reactome:R-HSA-9865196","Reactome:R-HSA-9006332","Reactome:R-HSA-8851933","Reactome:R-HSA-8937728","Reactome:R-HSA-1433418","Reactome:R-HSA-8875817","Reactome:R-HSA-2029989","Reactome:R-HSA-8942607","Reactome:R-HSA-5654397","Reactome:R-HSA-5607750","Reactome:R-HSA-399946","Reactome:R-HSA-5654418","Reactome:R-HSA-1671691","Reactome:R-HSA-2404199","Reactome:R-HSA-2424484","Reactome:R-HSA-879909","Reactome:R-HSA-9027272","Reactome:R-HSA-373747","Reactome:R-HSA-210291","Reactome:R-HSA-202291","Reactome:R-HSA-2730860","Reactome:R-HSA-389083","Reactome:R-HSA-389762","Reactome:R-HSA-434836","Reactome:R-HSA-5654147","Reactome:R-HSA-9665704","Reactome:R-HSA-9700186","Reactome:R-HSA-2029459","Reactome:R-HSA-1251922","Reactome:R-HSA-9673761","Reactome:R-HSA-5690702","Reactome:R-HSA-8851890","Reactome:R-HSA-9712082","Reactome:R-HSA-186786","Reactome:R-HSA-8937844","Reactome:R-HSA-5683930","Reactome:R-HSA-1168394","Reactome:R-HSA-8857555","Reactome:R-HSA-2396594","Reactome:R-HSA-9011241","Reactome:R-HSA-2730851","Reactome:R-HSA-3215391","Reactome:R-HSA-191636","Reactome:R-HSA-4420206","Reactome:R-HSA-2023460","Reactome:R-HSA-508282","Reactome:R-HSA-2033485","Reactome:R-HSA-8874080","Reactome:R-HSA-9029151","Reactome:R-HSA-9665389","Reactome:R-HSA-9842648","Reactome:R-HSA-2029453","Reactome:R-HSA-1225952","Reactome:R-HSA-1307963","Reactome:R-HSA-9606159","Reactome:R-HSA-429441","Reactome:R-HSA-9612996","Reactome:R-HSA-8964242","Reactome:R-HSA-210872","Reactome:R-HSA-3928578","Reactome:R-HSA-1433488","Reactome:R-HSA-202307","Reactome:R-HSA-2424487","Reactome:R-HSA-5621370","Reactome:R-HSA-191062","Reactome:R-HSA-202233","Reactome:R-HSA-2395412","Reactome:R-HSA-9613023","Reactome:R-HSA-5654628","Reactome:R-HSA-2454239","Reactome:R-HSA-174164","Reactome:R-HSA-377640","Reactome:R-HSA-68954","Reactome:R-HSA-9026510","Reactome:R-HSA-389159","Reactome:R-HSA-8857925","Reactome:R-HSA-9700193","Reactome:R-HSA-9732738","Reactome:R-HSA-354073","Reactome:R-HSA-171011","Reactome:R-HSA-399947","Reactome:R-HSA-8847977","Reactome:R-HSA-909726","Reactome:R-HSA-452097","Reactome:R-HSA-8876246","Reactome:R-HSA-9612085","Reactome:R-HSA-3928604","Reactome:R-HSA-5654428","Reactome:R-HSA-9603420","Reactome:R-HSA-2038387","Reactome:R-HSA-3928583","Reactome:R-HSA-9733323","Reactome:R-HSA-9842651","Reactome:R-HSA-2395801","Reactome:R-HSA-9026890","Reactome:R-HSA-909729","Reactome:R-HSA-182969","Reactome:R-HSA-8848436","Reactome:R-HSA-445076","Reactome:R-HSA-9606163","Reactome:R-HSA-1248655","Reactome:R-HSA-445085","Reactome:R-HSA-170070","Reactome:R-HSA-389086","Reactome:R-HSA-399934","Reactome:R-HSA-8855237","Reactome:R-HSA-9624014","Reactome:R-HSA-9672173","Reactome:R-HSA-8848873","Reactome:R-HSA-177937","Reactome:R-HSA-2033490","Reactome:R-HSA-389354","Reactome:R-HSA-8848005","Reactome:R-HSA-2012087","Reactome:R-HSA-1295540","Reactome:R-HSA-9034875","Reactome:R-HSA-9006323","Reactome:R-HSA-909732","Reactome:R-HSA-2730886","Reactome:R-HSA-9695834","Reactome:R-HSA-9712086","Reactome:R-HSA-2012073","Reactome:R-HSA-9831136","Reactome:R-HSA-5654634","Reactome:R-HSA-418859","Reactome:R-HSA-3928648","Reactome:R-HSA-202165","Reactome:R-HSA-354124","Reactome:R-HSA-8853313","Reactome:R-HSA-8956659","Reactome:R-HSA-9021609","Reactome:R-HSA-9026502","Reactome:R-HSA-9032426","Reactome:R-HSA-1433506","Reactome:R-HSA-202216","Reactome:R-HSA-5654578","Reactome:R-HSA-9033284","Reactome:R-HSA-8849042","Reactome:R-HSA-9665709","Reactome:R-HSA-9700647","Reactome:R-HSA-2428926","Reactome:R-HSA-983703","Reactome:R-HSA-391871","Reactome:R-HSA-1169421","Reactome:R-HSA-1472121","Reactome:R-HSA-1250348","Reactome:R-HSA-380780","Reactome:R-HSA-5654631","Reactome:R-HSA-8848124","Reactome:R-HSA-1250195","Reactome:R-HSA-1839098","Reactome:R-HSA-2730888","Reactome:R-HSA-452100","Reactome:R-HSA-873918","Reactome:R-HSA-9012650","Reactome:R-HSA-2023455","Reactome:R-HSA-5218809","Reactome:R-HSA-5357429","Reactome:R-HSA-1963586","Reactome:R-HSA-9861469","Reactome:R-HSA-190388","Reactome:R-HSA-2197698","Reactome:R-HSA-9698003","Reactome:R-HSA-5218830","Reactome:R-HSA-1247844","Reactome:R-HSA-873922","Reactome:R-HSA-114600","Reactome:R-HSA-2012082","Reactome:R-HSA-9700171","Reactome:R-HSA-452122","Reactome:R-HSA-2671742","Reactome:R-HSA-9670412","Reactome:R-HSA-2404193","Reactome:R-HSA-9700168","Reactome:R-HSA-1888198","Reactome:R-HSA-9860759","Reactome:R-HSA-1225960","Reactome:R-HSA-5654655","Reactome:R-HSA-8937807","Reactome:R-HSA-9018572","Reactome:R-HSA-4420117","Reactome:R-HSA-443817","Reactome:R-HSA-205289","Reactome:R-HSA-170991","Reactome:R-HSA-418163","Reactome:R-HSA-445084","Reactome:R-HSA-5218642","Reactome:R-HSA-5218851","Reactome:R-HSA-3928610","Reactome:R-HSA-5655278","Reactome:R-HSA-8848077","Reactome:R-HSA-8849032","Reactome:R-HSA-9037040","Reactome:R-HSA-9625487","Reactome:R-HSA-9665032","Reactome:R-HSA-9670418","Reactome:R-HSA-202168","Reactome:R-HSA-8848606","Reactome:R-HSA-201521","Reactome:R-HSA-2586555","Reactome:R-HSA-2424486","Reactome:R-HSA-6806974","Reactome:R-HSA-418872","Reactome:R-HSA-388833","Reactome:R-HSA-873924","Reactome:R-HSA-9606162","Reactome:R-HSA-8848726","Reactome:R-HSA-9664275","Reactome:R-HSA-9664588","MetaCyc:2.7.10.1-RXN","Reactome:R-HSA-2201322","Reactome:R-HSA-6784006","EC:2.7.10.-","Reactome:R-HSA-8867041","Reactome:R-HSA-9634390","Reactome:R-HSA-5654222","Reactome:R-HSA-9034814","Reactome:R-HSA-9665411","Reactome:R-HSA-9700181","Reactome:R-HSA-2730862","Reactome:R-HSA-5621355","Reactome:R-HSA-2671829","Reactome:R-HSA-9028728","Reactome:R-HSA-202248","Reactome:R-HSA-190429","Reactome:R-HSA-5218828","Reactome:R-HSA-2029984","Reactome:R-HSA-8983872","Reactome:R-HSA-9674567","Reactome:R-HSA-9703437","Reactome:R-HSA-170156","Reactome:R-HSA-9706344","Reactome:R-HSA-5218640","Reactome:R-HSA-5621363","Reactome:R-HSA-8848818","Reactome:R-HSA-9027273","Reactome:R-HSA-9664278","Reactome:R-HSA-9032854","Reactome:R-HSA-5655270","Reactome:R-HSA-8848758","Reactome:R-HSA-190413","Reactome:R-HSA-9673756","Reactome:R-HSA-1839065","Reactome:R-HSA-5654582","Reactome:R-HSA-9712085","Reactome:R-HSA-1295609","Reactome:R-HSA-202174","Reactome:R-HSA-5654149","Reactome:R-HSA-9664976","Reactome:R-HSA-9712087","Reactome:R-HSA-112333","Reactome:R-HSA-5624486","Reactome:R-HSA-912629","Reactome:R-HSA-190326","Reactome:R-HSA-8964252","Reactome:R-HSA-6790087","Reactome:R-HSA-5218812","Reactome:R-HSA-5654605","Reactome:R-HSA-5637795","Reactome:R-HSA-9669890","Reactome:R-HSA-190427","Reactome:R-HSA-9669911","Reactome:R-HSA-2730882","Reactome:R-HSA-2029268","Reactome:R-HSA-9699578","Reactome:R-HSA-5654408","Reactome:R-HSA-4420121","Reactome:R-HSA-6784319","Reactome:R-HSA-9674558","Reactome:R-HSA-9733314","Reactome:R-HSA-9842666","Reactome:R-HSA-8853325","Reactome:R-HSA-9726848","Reactome:R-HSA-2671850","Reactome:R-HSA-3928580","Reactome:R-HSA-8849463","Reactome:R-HSA-4093332","Reactome:R-HSA-1839112","Reactome:R-HSA-2454208","Reactome:R-HSA-2395439","Reactome:R-HSA-419646","Reactome:R-HSA-451942","Reactome:R-HSA-9665705","Reactome:R-HSA-9860500","Reactome:R-HSA-374701","Reactome:R-HSA-909718","Reactome:R-HSA-9706350","Reactome:R-HSA-1433542","Reactome:R-HSA-391865","Reactome:R-HSA-69195","Reactome:R-HSA-9842667","Reactome:R-HSA-983707","Reactome:R-HSA-9029155","Reactome:R-HSA-9762209","Reactome:R-HSA-879907","Reactome:R-HSA-190385","Reactome:R-HSA-3928627","Reactome:R-HSA-9841924","Reactome:R-HSA-1839067","Reactome:R-HSA-1839110","Reactome:R-HSA-5686587","Reactome:R-HSA-9032601","Reactome:R-HSA-9672175","Reactome:R-HSA-8948143","Reactome:R-HSA-9703438","Reactome:R-HSA-2730833","Reactome:R-HSA-2038944","Reactome:R-HSA-5655341","Reactome:R-HSA-9934751","Reactome:R-HSA-8857583","Reactome:R-HSA-8849102","Reactome:R-HSA-2033488","Reactome:R-HSA-432129","Reactome:R-HSA-202245","Reactome:R-HSA-5655284","Reactome:R-HSA-1248694","Reactome:R-HSA-8874082","Reactome:R-HSA-5218806","Reactome:R-HSA-8857577","Reactome:R-HSA-212710","Reactome:R-HSA-1963581","Reactome:R-HSA-2586553","Reactome:R-HSA-428888","Reactome:R-HSA-8876948","Reactome:R-HSA-8848975","Reactome:R-HSA-429449","Reactome:R-HSA-1524186","Reactome:R-HSA-5654545","Reactome:R-HSA-391156","Reactome:R-HSA-3928594","Reactome:R-HSA-5654151","Reactome:R-HSA-2033486","Reactome:R-HSA-5655268","Reactome:R-HSA-5655243","Reactome:R-HSA-177934","Reactome:R-HSA-1433454","Reactome:R-HSA-2730858","Reactome:R-HSA-5607745","Reactome:R-HSA-8853309","Reactome:R-HSA-9701488","Reactome:R-HSA-445091","Reactome:R-HSA-4420128","Reactome:R-HSA-909730","Reactome:R-HSA-9700164","Reactome:R-HSA-9680248","Reactome:R-HSA-9709918","Reactome:R-HSA-5654653","Reactome:R-HSA-5655301","Reactome:R-HSA-2029449","Reactome:R-HSA-9664261","Reactome:R-HSA-8876230","Reactome:R-HSA-9034714","Reactome:R-HSA-2730884","Reactome:R-HSA-8874078","Reactome:R-HSA-983709","Reactome:R-HSA-2130194","Reactome:R-HSA-190408","Reactome:R-HSA-183058","Reactome:R-HSA-9604767","Reactome:R-HSA-8849068","Reactome:R-HSA-5654575","Reactome:R-HSA-5654407","Reactome:R-HSA-5654607","Reactome:R-HSA-9024726","Reactome:R-HSA-5637796","Reactome:R-HSA-8875451","Reactome:R-HSA-1250315","Reactome:R-HSA-5218820","Reactome:R-HSA-9026464","Reactome:R-HSA-9698005","Reactome:R-HSA-2730843","Reactome:R-HSA-9027425","Reactome:R-HSA-982807"],"synonyms":[{"name":"protein-tyrosine kinase activity","type":"exact"}],"termid":"GO:0004713","terms_by_termid":{"GO:0004713":null}}


id: PR:O13903
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An exosome complex component RRP40 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00475","PRO:DNx","PANTHER:PTHR21321:SF1"],"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":"exosome complex component rrp40 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22A12.12c","secondary_identifiers":["UniProtKB:O13903"],"synonyms":[{"name":"Spom972h-EXOSC3","type":"exact"},{"name":"ribosomal RNA-processing protein 40 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13903"}


id: GO:0010804
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate or extent of the tumor necrosis factor-mediated signaling pathway. The tumor necrosis factor-mediated signaling pathway is the series of molecular signals generated as a consequence of tumor necrosis factor binding to a cell surface receptor.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine-mediated signaling pathway","termid":"GO:0001960"},{"relation_name":"is_a","term_name":"regulation of tumor necrosis factor-mediated signaling pathway","termid":"GO:0010803"},{"relation_name":"negatively_regulates","term_name":"tumor necrosis factor-mediated signaling pathway","termid":"GO:0033209"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of tumor necrosis factor-mediated signaling pathway","synonyms":[{"name":"negative regulation of TNF signaling","type":"exact"},{"name":"negative regulation of TNF-mediated signaling pathway","type":"exact"},{"name":"negative regulation of tumor necrosis factor-mediated signalling pathway","type":"exact"}],"termid":"GO:0010804"}


id: PBO:0000553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin","termid":"PBO:0000553"}


id: PATO:0001043
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in an entity by virtue of the bearer's propensity to resist an external stimulus.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitivity toward","termid":"PATO:0000085"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"susceptibility toward","synonyms":[{"name":"susceptibility","type":"exact"}],"termid":"PATO:0001043"}


id: FYPO:0001005
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which DNA is broken into small fragments when the cell is subject to nitrogen starvation.","definition_xrefs":["PMID:19366728","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fragmented DNA","termid":"FYPO:0000160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"fragmented DNA during nitrogen starvation","synonyms":[{"name":"DNA fragmentation during nitrogen starvation","type":"exact"},{"name":"fragmented DNA during nitrogen depletion","type":"exact"},{"name":"fragmented DNA during nitrogen deprivation","type":"exact"},{"name":"fragmented nucleus during nitrogen starvation","type":"related"}],"termid":"FYPO:0001005"}


id: MONDO:0015921
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ARX-related epileptic encephalopathy (obsolete MONDO:0015921)","secondary_identifiers":["Orphanet:182079"],"termid":"MONDO:0015921","xrefs":{"Monarch":{"xref_id":"0015921"}}}


id: GO:0005755
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete hydrogen-transporting ATP synthase, coupling factor CF(0) (obsolete GO:0005755)","synonyms":[{"name":"hydrogen-transporting ATP synthase, coupling factor CF(0)","type":"exact"}],"termid":"GO:0005755"}


id: GO:2000794
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of epithelial cell proliferation involved in lung morphogenesis.","definition_xrefs":["PMID:21513708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation","termid":"GO:0050678"},{"relation_name":"regulates","term_name":"epithelial cell proliferation involved in lung morphogenesis","termid":"GO:0060502"}],"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 epithelial cell proliferation involved in lung morphogenesis","termid":"GO:2000794"}


id: PBO:0062447
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 E member 111 pseudogene","termid":"PBO:0062447"}


id: MONDO:0017918
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome is a very rare neurological condition. The few patients described in the medical literature were characterized by brain anomalies; an unusual face with broad nasal root, wide spaced eyes (hypertelorism) and a very small chin (micrognathia); failure to thrive; severe intellectual disability ;and lack of muscle tone (hypotonia). Exams of the brain showed a poor development (hypoplasia) of the pale part of the brain known as white matter, and an absent or abnormal corpus callosum (nerve fibers joining the two hemispheres of the brain). Only a few cases have being described. The cause is unknown but may be related to a disorder of axonal development. The described cases seem to be inherited in an autosomal recessive or X-linked way. Corpus callosum agenesis is one of the more frequent congenital malformations. It can be either asymptomatic or associated with intellectual disability, epilepsy, or psychiatric syndromes. It can be part of several genetic syndromes, such as Aicardi syndrome, Andermann syndrome and Apert syndrome, trisomies 13, 18 ; or result from metabolic causes; drugs (cocaine); or viral infection (influenza). Many patients with corpus callosum anomalies have other brain anomalies, including white matter hypoplasia. There is no information on specific treatment for this condition.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome","secondary_identifiers":["MEDGEN:419038","Orphanet:3207","UMLS:C2931292","GARD:12488","MESH:C536701"],"synonyms":[{"name":"Curatolo Cilio Pessagno syndrome","type":"related"},{"name":"Curatolo-Cilio-Pessagno syndrome","type":"exact"},{"name":"familial white matter hypoplasia, agenesis of the corpus callosum, intellectual disability and growth deficiency","type":"related"}],"termid":"MONDO:0017918","xrefs":{"Monarch":{"xref_id":"0017918"}}}


id: PBO:0002049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U5 snRNP-associated protein Aar2 (predicted)","termid":"PBO:0002049"}


id: MONDO:0008362
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":"ragweed sensitivity","secondary_identifiers":["UMLS:C1867394","MEDGEN:356768","OMIM:179450","MESH:C566725"],"synonyms":[{"name":"ragweed sensitivity","type":"exact"}],"termid":"MONDO:0008362","xrefs":{"Monarch":{"xref_id":"0008362"}}}


id: MONDO:0023663
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete macrocephaly mesodermal hamartoma spectrum (obsolete MONDO:0023663)","secondary_identifiers":["MESH:C537716"],"synonyms":[{"name":"Elattoproteus syndrome","type":"related"},{"name":"gigantism, partial, of hands and feet, nevi, hemihypertrophy, and macrocephaly","type":"related"},{"name":"hemihypertrophy and macrocephaly","type":"related"},{"name":"partial gigantism of hands and feet, nevi, hemihypertrophy, macrocephaly","type":"related"}],"termid":"MONDO:0023663","xrefs":{"Monarch":{"xref_id":"0023663"}}}


id: PBO:0001261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk13 (predicted)","termid":"PBO:0001261"}


id: GO:0005602
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of six subunits of C1q, each formed of the three homologous polypeptide chains C1QA, C1QB, and C1QB, and tetramer of two C1QR and two C1QS polypeptide chains.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"extracellular region","termid":"GO:0005576"}],"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:0005576"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005576"],"is_obsolete":false,"name":"complement component C1 complex","synonyms":[{"name":"complement component C1q complex","type":"narrow"}],"termid":"GO:0005602"}


id: GO:0098035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The encapsulation of the viral DNA genome within the capsid, which proceeds via cleavage of the viral DNA at specific sites by a viral terminase.","definition_xrefs":["GOC:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral DNA genome packaging","termid":"GO:0019073"}],"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":"viral DNA genome packaging via site-specific sequence recognition","termid":"GO:0098035"}


id: GO:0030245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of cellulose, a linear beta1-4 glucan of molecular mass 50-400 kDa with the pyranose units in the -4C1 conformation.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellulose metabolic process","termid":"GO:0030243"},{"relation_name":"is_a","term_name":"beta-glucan catabolic process","termid":"GO:0051275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"cellulose catabolic process","secondary_identifiers":["GO:0016179"],"synonyms":[{"name":"cellulose breakdown","type":"exact"},{"name":"cellulose catabolism","type":"exact"},{"name":"cellulose degradation","type":"exact"}],"termid":"GO:0030245"}


id: GO:0006781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions that utilize succinyl-CoA in the synthesis of protoporphyrin IX.","definition_xrefs":["GOC:isa_complete","ISBN:0879010479"],"direct_ancestors":[{"relation_name":"is_a","term_name":"succinyl-CoA metabolic process","termid":"GO:0006104"},{"relation_name":"is_a","term_name":"porphyrin-containing compound biosynthetic process","termid":"GO:0006779"},{"relation_name":"part_of","term_name":"uroporphyrinogen III biosynthetic process","termid":"GO:0006780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"part_of","termid":"GO:0044281"},{"rel_name":"part_of","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0033013","GO:0008150","GO:0006790"],"is_obsolete":false,"name":"succinyl-CoA pathway","synonyms":[{"name":"biosynthesis of protoporphyrin IX via succinyl CoA","type":"exact"},{"name":"biosynthesis of protoporphyrin IX via succinyl-CoA","type":"exact"},{"name":"biosynthetic process of protoporphyrin IX via succinyl CoA","type":"exact"},{"name":"biosynthetic process of protoporphyrin IX via succinyl-CoA","type":"exact"},{"name":"succinyl CoA pathway","type":"exact"}],"termid":"GO:0006781"}


id: PBO:0086520
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; conserved across S. cerevisiae strains; partially overlaps dubious ORF YFL015W-A; YFL015C is not an essential gene","termid":"PBO:0086520"}


id: PBO:0080733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WW domain containing oxidoreductase","termid":"PBO:0080733"}


id: PBO:0047287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibronectin type III and ankyrin repeat domains 1","termid":"PBO:0047287"}


id: PBO:0076446
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 2","termid":"PBO:0076446"}


id: GO:0018993
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The determination of sex and sexual phenotypes in an organism's soma.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sex determination","termid":"GO:0007530"},{"relation_name":"part_of","term_name":"multicellular organism development","termid":"GO:0007275"}],"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":"somatic sex determination","termid":"GO:0018993"}


id: PBO:0086376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative ATPase containing the DEAD/H helicase-related sequence motif; null mutant displays increased levels of spontaneous Rad52p foci; SWAT-GFP and mCherry fusion proteins localize to the nucleus","termid":"PBO:0086376"}


id: PBO:0076385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transforming acidic coiled-coil containing protein 2","termid":"PBO:0076385"}


id: MOD:00248
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-cysteine residue and an L-phenylalanine residue to form L-phenylalanine thiazole-4-carboxylic acid.","definition_xrefs":["RESID:AA0243","PubMed:1880060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiazole/thiazoline ring crosslinked residues","termid":"MOD:01420"},{"relation_name":"is_a","term_name":"didehydrogenated residue","termid":"MOD:01888"},{"relation_name":"is_a","term_name":"crosslinked L-phenylalanine residue","termid":"MOD:02053"}],"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":"L-phenylalanine thiazole-4-carboxylic acid","synonyms":[{"name":"2-[(1S)-1-amino-2-phenylethyl]-1,3-thiazole-4-carboxylic acid","type":"exact"},{"name":"2-[1-azanyl-2-phenylethyl]-1,3-thiazole-4-carboxylic acid","type":"exact"},{"name":"CROSSLNK Thiazole-4-carboxylic acid (Phe-Cys)","type":"exact"},{"name":"L-phenylalanine thiazole-4-carboxylic acid","type":"exact"}],"termid":"MOD:00248"}


id: MONDO:0013882
data:
  {"annotated_genes":["SJAG_03506"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88082],"is_not":false,"summary":null,"term":"MONDO:0013882"}]},"cv_name":"mondo","definition":"Any hyperphosphatasia-intellectual disability syndrome in which the cause of the disease is a mutation in the PIGO gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperphosphatasia-intellectual disability syndrome","termid":"MONDO:0016596"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03506":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"hyperphosphatasia with intellectual disability syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3553637","GARD:18351","DOID:0070434","MEDGEN:766551","OMIM:614749"],"synonyms":[{"name":"HPMRS2","type":"related"},{"name":"PIGO hyperphosphatasia-intellectual disability syndrome","type":"exact"},{"name":"glycosylphosphatidylinositol biosynthesis defect 6","type":"related"},{"name":"hyperphosphatasia with intellectual disability syndrome 2","type":"exact"},{"name":"hyperphosphatasia with intellectual disability syndrome type 2","type":"exact"},{"name":"hyperphosphatasia with mental retardation syndrome 2","type":"exact"},{"name":"hyperphosphatasia with mental retardation syndrome type 2","type":"exact"},{"name":"hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGO","type":"exact"}],"termid":"MONDO:0013882","terms_by_termid":{"MONDO:0013882":null},"xrefs":{"Monarch":{"xref_id":"0013882"}}}


id: MONDO:0012064
data:
  {"annotated_genes":["SJAG_04222"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87530],"is_not":false,"summary":null,"term":"MONDO:0012064"}]},"cv_name":"mondo","definition":"Choanal atresia - deafness - cardiac defects - dysmorphism syndrome, also known as Burn-McKeown syndrome, is an extremely rare multiple congenital anomaly syndrome characterized by bilateral choanal atresia associated with a characteristic cranio-facial dysmorphism (hypertelorism with narrow palpebral fissures, coloboma of inferior eyelid with presence of eyelashes medial to the defect, prominent nasal bridge, thin lips, prominent ears), that can be accompanied by hearing loss, unilateral cleft lip, preauricular tags, cardiac septal defects and anomalies of the kidneys. The features of this syndrome overlaps considerably with those of the CHARGE syndrome.","definition_xrefs":["Orphanet:1200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04222":null},"genotype_count":0,"is_obsolete":false,"name":"choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1837822","OMIM:608572","DOID:0080695","MEDGEN:325265","GARD:10041","MESH:C563682"],"synonyms":[{"name":"BMKS","type":"related"},{"name":"Burn-McKeown syndrome","type":"exact"},{"name":"bilateral choanal atresia, cardiac defects, deafness, and dysmorphic appearance","type":"related"},{"name":"choanal atresia deafness cardiac defects dysmorphism","type":"related"},{"name":"oculootofacial dysplasia","type":"exact"}],"termid":"MONDO:0012064","terms_by_termid":{"MONDO:0012064":null},"xrefs":{"Monarch":{"xref_id":"0012064"}}}


id: MONDO:0859332
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex cortical dysplasia with other brain malformations","termid":"MONDO:0000904"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortical dysplasia, complex, with other brain malformations 11","secondary_identifiers":["UMLS:C5774270","MEDGEN:1824043","OMIM:620156"],"termid":"MONDO:0859332","xrefs":{"Monarch":{"xref_id":"0859332"}}}


id: PBO:0035819
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-loss_of_punctate_nuclear_protein_localization","termid":"PBO:0035819"}


id: PBO:0041082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"break repair meiotic recombinase recruitment factor 1","termid":"PBO:0041082"}


id: MONDO:0010787
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Kearns-Sayre syndrome (KSS) is a mitochondrial disease characterized by progressive external ophthalmoplegia (PEO), pigmentary retinitis and an onset before the age of 20 years. Common additional features include deafness, cerebellar ataxia and heart block.","definition_xrefs":["Orphanet:480"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"progressive external ophthalmoplegia","termid":"MONDO:0005181"},{"relation_name":"is_a","term_name":"familial dilated cardiomyopathy","termid":"MONDO:0016333"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"disorder of visual system","termid":"MONDO:0024458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005336","MONDO:0004069","MONDO:0002320","MONDO:0005267","MONDO:0005244"],"is_obsolete":false,"name":"Kearns-Sayre syndrome","secondary_identifiers":["NORD:1323","OMIM:530000","MedDRA:10048804","SCTID:25792000","ICD10CM:H49.81","NANDO:1201064","MEDGEN:9618","GARD:6817","NCIT:C84798","UMLS:C0022541","icd11.foundation:399100745","MESH:D007625","DOID:12934","NANDO:2200529"],"synonyms":[{"name":"CPEO with myopathy","type":"related"},{"name":"CPEO with ragged red fibers","type":"related"},{"name":"CPEO with ragged red fibres","type":"related"},{"name":"CPEO with ragged-Red fibers","type":"related"},{"name":"CPEO with ragged-Red fibres","type":"related"},{"name":"KSS","type":"related"},{"name":"Kearns Sayre Syndrome","type":"exact"},{"name":"Kearns-Sayre syndrome","type":"exact"},{"name":"chronic progressive external ophthalmoplegia with myopathy","type":"related"},{"name":"mitochondrial Cytopathy","type":"related"},{"name":"oculocraniosomatic syndrome","type":"related"},{"name":"ophthalmoplegia plus syndrome","type":"related"},{"name":"ophthalmoplegia, pigmentary Degeneration of retina, and cardiomyopathy","type":"related"},{"name":"ophthalmoplegia, progressive external, with ragged red fibers","type":"related"},{"name":"ophthalmoplegia, progressive external, with ragged red fibres","type":"related"},{"name":"ophthalmoplegia, progressive external, with ragged-Red fibers","type":"related"},{"name":"ophthalmoplegia, progressive external, with ragged-Red fibres","type":"related"},{"name":"ophthalmoplegia-plus syndrome","type":"related"}],"termid":"MONDO:0010787","xrefs":{"Monarch":{"xref_id":"0010787"}}}


id: GO:1900137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of chemokine activity.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell migration","termid":"GO:0030336"},{"relation_name":"is_a","term_name":"negative regulation of chemotaxis","termid":"GO:0050922"},{"relation_name":"is_a","term_name":"negative regulation of cytokine activity","termid":"GO:0060302"},{"relation_name":"is_a","term_name":"regulation of chemokine activity","termid":"GO:1900136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of chemokine activity","synonyms":[{"name":"down regulation of chemokine activity","type":"exact"},{"name":"down-regulation of chemokine activity","type":"exact"},{"name":"downregulation of chemokine activity","type":"exact"},{"name":"inhibition of chemokine activity","type":"narrow"}],"termid":"GO:1900137"}


id: GO:1902073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hypoxia-inducible factor-1alpha signaling pathway.","definition_xrefs":["PMID:21685248","GOC:bf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hypoxia-inducible factor-1alpha signaling pathway","termid":"GO:1902071"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"hypoxia-inducible factor-1alpha signaling pathway","termid":"GO:0097411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of hypoxia-inducible factor-1alpha signaling pathway","synonyms":[{"name":"activation of HIF1alpha pathway","type":"exact"},{"name":"activation of hypoxia-inducible factor-1alpha signaling pathway","type":"narrow"},{"name":"activation of hypoxia-inducible factor-1alpha signalling pathway","type":"exact"},{"name":"hypoxic stabilization of HIF1A","type":"narrow"},{"name":"positive regulation of HIF1alpha pathway","type":"exact"},{"name":"positive regulation of hypoxia-inducible factor-1alpha signalling pathway","type":"exact"},{"name":"up regulation of HIF1alpha pathway","type":"exact"},{"name":"up regulation of hypoxia-inducible factor-1alpha signaling pathway","type":"exact"},{"name":"up regulation of hypoxia-inducible factor-1alpha signalling pathway","type":"exact"},{"name":"up-regulation of HIF1alpha pathway","type":"exact"},{"name":"up-regulation of hypoxia-inducible factor-1alpha signaling pathway","type":"exact"},{"name":"up-regulation of hypoxia-inducible factor-1alpha signalling pathway","type":"exact"},{"name":"upregulation of HIF1alpha pathway","type":"exact"},{"name":"upregulation of hypoxia-inducible factor-1alpha signaling pathway","type":"exact"},{"name":"upregulation of hypoxia-inducible factor-1alpha signalling pathway","type":"exact"}],"termid":"GO:1902073"}


id: GO:0150142
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of CD86 biosynthetic process.","definition_xrefs":["GOC:aruk"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of CD86 production (obsolete GO:0150142)","synonyms":[{"name":"positive regulation of CD86 biosynthetic process","type":"exact"}],"termid":"GO:0150142"}


id: MONDO:0005289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the paranasal sinuses. Representative examples of benign neoplasms include Schneiderian papilloma and salivary gland-type adenoma. Representative examples of malignant neoplasms include carcinoma and lymphoma.","definition_xrefs":["NCIT:C7488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paranasal sinus disorder","termid":"MONDO:0001735"},{"relation_name":"is_a","term_name":"skull neoplasm","termid":"MONDO:0024653"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paranasal sinus neoplasm","secondary_identifiers":["UMLS:C0030470","MEDGEN:18296","DOID:1350","HP:0030072","EFO:0003866","SCTID:126675008"],"synonyms":[{"name":"accessory sinus neoplasm","type":"exact"},{"name":"accessory sinus tumor","type":"exact"},{"name":"accessory sinus tumour","type":"exact"},{"name":"neoplasm of accessory sinus","type":"exact"},{"name":"neoplasm of paranasal sinus","type":"exact"},{"name":"neoplasm of the accessory sinus","type":"exact"},{"name":"neoplasm of the paranasal sinus","type":"exact"},{"name":"paranasal sinus neoplasm","type":"exact"},{"name":"paranasal sinus neoplasm (disease)","type":"exact"},{"name":"paranasal sinus neoplasms","type":"exact"},{"name":"paranasal sinus tumor","type":"exact"},{"name":"paranasal sinus tumour","type":"exact"},{"name":"tumor of accessory sinus","type":"exact"},{"name":"tumor of paranasal sinus","type":"exact"},{"name":"tumor of the accessory sinus","type":"exact"},{"name":"tumor of the paranasal sinus","type":"exact"},{"name":"tumour of accessory sinus","type":"exact"},{"name":"tumour of paranasal sinus","type":"exact"},{"name":"tumour of the accessory sinus","type":"exact"},{"name":"tumour of the paranasal sinus","type":"exact"}],"termid":"MONDO:0005289","xrefs":{"Monarch":{"xref_id":"0005289"}}}


id: PBO:0054006
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 1335","termid":"PBO:0054006"}


id: PR:Q10085
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC11D3.06 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10085"],"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 transporter C11D3.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11D3.06","synonyms":[{"name":"Spom972h-SPAC11D3.06","type":"exact"}],"termid":"PR:Q10085"}


id: MONDO:0011531
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome","termid":"MONDO:0018997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005046"],"is_obsolete":false,"name":"Noonan syndrome 2","secondary_identifiers":["DOID:0060580","NCIT:C176930","MESH:C548081","MEDGEN:344290","UMLS:C1854469","GARD:10698","OMIM:605275"],"synonyms":[{"name":"NS2","type":"exact"},{"name":"Noonan syndrome 2","type":"exact"},{"name":"Noonan syndrome autosomal recessive","type":"related"},{"name":"Noonan syndrome type 2","type":"exact"},{"name":"Noonan syndrome, autosomal recessive","type":"related"},{"name":"autosomal recessive Noonan syndrome","type":"related"}],"termid":"MONDO:0011531","xrefs":{"Monarch":{"xref_id":"0011531"}}}


id: PBO:0120125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitotic spindle midzone-localized microtubule bundling protein; microtubule-associated protein (MAP) family member; required for anaphase spindle elongation and stabilization; selectively increases the lifetime of antiparallel microtubule overlaps; undergoes cell cycle-regulated degradation by anaphase promoting complex; relative distribution to microtubules decreases upon DNA replication stress","termid":"PBO:0120125"}


id: PBO:0048056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin heavy chain 1 pseudogene 5","termid":"PBO:0048056"}


id: GO:0033542
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A fatty acid beta-oxidation pathway by which fatty acids having cis-double bonds on even-numbered carbons are degraded. Fatty acid beta-oxidation begins with the addition of coenzyme A to a fatty acid, and ends when only two or three carbons remain (as acetyl-CoA or propionyl-CoA respectively).","definition_xrefs":["MetaCyc:PWY-5138","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid beta-oxidation","termid":"GO:0006635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"fatty acid beta-oxidation, unsaturated, even number","termid":"GO:0033542"}


id: MONDO:0018420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"autosomal recessive spastic paraplegia type 68","secondary_identifiers":["Orphanet:401825"],"synonyms":[{"name":"SPG68","type":"exact"}],"termid":"MONDO:0018420","xrefs":{"Monarch":{"xref_id":"0018420"}}}


id: PBO:0054551
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 1951","termid":"PBO:0054551"}


id: PBO:0057297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 513a-2","termid":"PBO:0057297"}


id: MONDO:0019133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome is characterized by facial dysmorphology, neuropathic visceral dysmotility, neurogenic megacystis, intracerebral calcifications and developmental delay. It has been described in two siblings (brother and sister) born to consanguineous parents. The girl also had microcephaly and multicystic kidneys. The boy had a more extensive neuropathic visceral disorder, leading clinically to chronic intestinal pseudo-obstruction syndrome (CIPO).","definition_xrefs":["Orphanet:73246"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome","secondary_identifiers":["UMLS:C4304402","MEDGEN:930071","GARD:18923"],"termid":"MONDO:0019133","xrefs":{"Monarch":{"xref_id":"0019133"}}}


id: PATO:0002631
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An occurrence of a process during which time there is an inability to change the course, extent, or repetition of the process.","definition_xrefs":["PATO:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"occurrence","termid":"PATO:0000057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"refractory","termid":"PATO:0002631"}


id: GO:0046296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycolate, the anion of hydroxyethanoic acid (glycolic acid).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolate metabolic process","termid":"GO:0009441"},{"relation_name":"is_a","term_name":"primary alcohol catabolic process","termid":"GO:0034310"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"glycolate catabolic process","synonyms":[{"name":"glycolate breakdown","type":"exact"},{"name":"glycolate catabolism","type":"exact"},{"name":"glycolate degradation","type":"exact"}],"termid":"GO:0046296"}


id: PBO:0053825
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 1089","termid":"PBO:0053825"}


id: PBO:0117107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RFX2 antisense RNA 2","termid":"PBO:0117107"}


id: MONDO:0008344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary edema of mountaineers, susceptibility to","secondary_identifiers":["ICD9:993.2","OMIM:178400","UMLS:C0340552","ICD9:416.8","SCTID:233954004","MEDGEN:83314","MESH:C535833"],"synonyms":[{"name":"HAPH","type":"related"},{"name":"high altitude pulmonary hypertension","type":"related"},{"name":"pulmonary edema of mountaineers","type":"related"},{"name":"pulmonary edema of mountaineers, susceptibility to","type":"exact"},{"name":"pulmonary oedema of mountaineers","type":"related"}],"termid":"MONDO:0008344","xrefs":{"Monarch":{"xref_id":"0008344"}}}


id: GO:1903423
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of synaptic vesicle recycling.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:22745285","GOC:PARL","GOC:pad"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of transport","termid":"GO:0051050"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle recycling","termid":"GO:1903421"},{"relation_name":"positively_regulates","term_name":"synaptic vesicle recycling","termid":"GO:0036465"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of synaptic vesicle recycling","synonyms":[{"name":"activation of kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"activation of kiss-and-stay synaptic vesicle recycling","type":"narrow"},{"name":"activation of synaptic vesicle recycling","type":"narrow"},{"name":"positive regulation of kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"positive regulation of kiss-and-stay synaptic vesicle recycling","type":"narrow"},{"name":"up regulation of kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"up regulation of kiss-and-stay synaptic vesicle recycling","type":"narrow"},{"name":"up regulation of synaptic vesicle recycling","type":"exact"},{"name":"up-regulation of kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"up-regulation of kiss-and-stay synaptic vesicle recycling","type":"narrow"},{"name":"up-regulation of synaptic vesicle recycling","type":"exact"},{"name":"upregulation of kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"upregulation of kiss-and-stay synaptic vesicle recycling","type":"narrow"},{"name":"upregulation of synaptic vesicle recycling","type":"exact"}],"termid":"GO:1903423"}


id: PBO:0082380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Beta 1 subunit of the 20S proteasome; responsible for cleavage after acidic residues in peptides","termid":"PBO:0082380"}


id: PBO:0003397
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Suppressor of Activated Ras1","termid":"PBO:0003397"}


id: MONDO:0003571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete labyrinthine dysfunction (obsolete MONDO:0003571)","secondary_identifiers":["SCTID:5239005","ICD9:386.58","ICD10CM:H83.2","DOID:566","ICD9:386.5","ICD9:386.50"],"termid":"MONDO:0003571","xrefs":{"Monarch":{"xref_id":"0003571"}}}


id: PBO:0087845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TLC1 RNA-associated factor involved in telomere length regulation; recruitment subunit of telomerase; has G-quadruplex promoting activity required for telomere elongation; role in activating telomere-bound Est2p-TLC1-RNA; EST1 has a paralog, EBS1, that arose from the whole genome duplication","termid":"PBO:0087845"}


id: PBO:0041538
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 78","termid":"PBO:0041538"}


id: MONDO:0012248
data:
  {"annotated_genes":["SJAG_01491"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87112],"is_not":false,"summary":null,"term":"MONDO:0012248"}]},"cv_name":"mondo","definition":"Autosomal recessive limb-girdle muscular dystrophy type 2K (LGMD2K) is a form of limb-girdle muscular dystrophy characterized by the onset of slowly progressive proximal muscle weakness during childhood (with fatigue and difficulty running and climbing stairs) and developmental delay. Mild intellectual deficit and microcephaly, without any obvious structural brain abnormality, are found in all patients. Mild pseudohypertrophy and joint contractures of the ankles have also been reported.","definition_xrefs":["Orphanet:86812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type C","termid":"MONDO:0000173"},{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of protein O-mannosyltransferase 1","termid":"MONDO:0016184"},{"relation_name":"is_a","term_name":"myopathy caused by variation in POMT1","termid":"MONDO:0700070"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01491":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0002320","MONDO:0005066","MONDO:0024322","MONDO:0005336"],"is_obsolete":false,"name":"autosomal recessive limb-girdle muscular dystrophy type 2K","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:12535","UMLS:C1836373","DOID:0110297","NCIT:C133730","OMIM:609308","MEDGEN:332193","SCTID:720523006"],"synonyms":[{"name":"LGMD-POMT1 related","type":"exact"},{"name":"LGMD2K","type":"exact"},{"name":"MDDGC1","type":"exact"},{"name":"POMT1 autosomal recessive limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT1","type":"exact"},{"name":"limb-girdle muscular dystrophy - intellectual disability","type":"related"},{"name":"limb-girdle muscular dystrophy type 2K","type":"related"},{"name":"limb-girdle muscular dystrophy-intellectual disability syndrome","type":"exact"},{"name":"muscular dystrophy limb-girdle type 2K","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 2K","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (Limb-girdle) type C, 1","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1","type":"related"}],"termid":"MONDO:0012248","terms_by_termid":{"MONDO:0012248":null},"xrefs":{"Monarch":{"xref_id":"0012248"}}}


id: GO:0034437
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of a glycoprotein from one side of a membrane to the other.","definition_xrefs":["GOC:mah","GOC:rl","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete glycoprotein transmembrane transporter activity (obsolete GO:0034437)","synonyms":[{"name":"glycoprotein transporter activity","type":"related"}],"termid":"GO:0034437"}


id: PBO:0079949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 3","termid":"PBO:0079949"}


id: GO:0044167
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding the host cell endoplasmic reticulum.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell membrane","termid":"GO:0033644"},{"relation_name":"part_of","term_name":"host cell endomembrane system","termid":"GO:0033645"},{"relation_name":"part_of","term_name":"host cell endoplasmic reticulum","termid":"GO:0044165"}],"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":"host cell endoplasmic reticulum membrane","synonyms":[{"name":"host endoplasmic reticulum membrane","type":"exact"}],"termid":"GO:0044167"}


id: PBO:0033777
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_chromatin_organization_resulting_in_peripheral_chromatin_distribution","termid":"PBO:0033777"}


id: PBO:0083184
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 the Ty1 long terminal repeat, YPRWdelta12","termid":"PBO:0083184"}


id: SO:0001539
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that affects the functioning of a translational product with respect to a reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_abnormal","termid":"SO:0002218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translational_product_function_variant","synonyms":[{"name":"translational product variant","type":"exact"}],"termid":"SO:0001539"}


id: PBO:0054924
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 2338","termid":"PBO:0054924"}


id: FYPO:0006766
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the phosphorylation of one or more specific proteins occurs to a lower extent than normal during the meiotic cell cycle, in cells that have not arrested the meiotic cell cycle under conditions that normally trigger meiotic DNA replication checkpoint signaling and response.","definition_xrefs":["PMID:10521402","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during meiotic cell cycle","termid":"FYPO:0005577"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"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:0002274"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002494","FYPO:0005447","FYPO:0000002","FYPO:0002274"],"is_obsolete":false,"name":"decreased protein phosphorylation in absence of meiotic DNA replication checkpoint arrest","synonyms":[{"name":"decreased protein phosphorylation with abolished meiotic DNA replication checkpoint arrest","type":"exact"},{"name":"reduced protein phosphorylation in absence of meiotic DNA replication checkpoint arrest","type":"exact"}],"termid":"FYPO:0006766"}


id: PBO:0028242
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_swollen_vacuolated_spheroid_vegetative_cell","termid":"PBO:0028242"}


id: MONDO:0013986
data:
  {"annotated_genes":["SJAG_02615"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88978],"is_not":false,"summary":null,"term":"MONDO:0013986"}]},"cv_name":"mondo","definition":"Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the FARS2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02615":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation defect type 14","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:319519","DOID:0111477","OMIM:614946","MEDGEN:1663069","UMLS:C4755312","GARD:17455"],"synonyms":[{"name":"COXPD14","type":"exact"},{"name":"FARS2 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 14","type":"related"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in FARS2","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 14","type":"exact"}],"termid":"MONDO:0013986","terms_by_termid":{"MONDO:0013986":null},"xrefs":{"Monarch":{"xref_id":"0013986"}}}


id: RO:0002226
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x develops_in y if x is located in y whilst x is developing","direct_ancestors":[{"relation_name":"is_a","term_name":"developmentally_preceded_by","termid":"RO:0002258"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"develops_in","termid":"RO:0002226"}


id: GO:0031408
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of any oxylipin, any of a group of biologically active compounds formed by oxidative metabolism of polyunsaturated fatty acids.","definition_xrefs":["GOC:mah","PMID:11960741"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxylipin metabolic process","termid":"GO:0031407"},{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"oxylipin biosynthetic process","synonyms":[{"name":"oxylipin anabolism","type":"exact"},{"name":"oxylipin biosynthesis","type":"exact"},{"name":"oxylipin formation","type":"exact"},{"name":"oxylipin synthesis","type":"exact"}],"termid":"GO:0031408"}


id: PBO:0066590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ras homolog family member D","termid":"PBO:0066590"}


id: PBO:0058430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4800","termid":"PBO:0058430"}


id: SO:0000866
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A frameshift caused by deleting one base.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"frameshift","termid":"SO:0000865"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minus_1_frameshift","synonyms":[{"name":"minus 1 frameshift","type":"exact"}],"termid":"SO:0000866"}


id: MONDO:0002975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A melanoma that arises usually from the breast skin and less often from the breast glandular tissue. Primary breast melanomas are rare.","definition_xrefs":["NCIT:C8410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanoma","termid":"MONDO:0005105"},{"relation_name":"is_a","term_name":"breast cancer","termid":"MONDO:0007254"}],"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":"malignant breast melanoma","secondary_identifiers":["MEDGEN:138069","SCTID:188050009","DOID:4364","UMLS:C0346787"],"synonyms":[{"name":"breast melanoma","type":"exact"},{"name":"breast melanoma (disease)","type":"exact"},{"name":"malignant breast melanoma","type":"exact"},{"name":"malignant melanoma of breast","type":"exact"},{"name":"malignant melanoma of the breast","type":"exact"},{"name":"melanoma (disease) of breast","type":"exact"}],"termid":"MONDO:0002975","xrefs":{"Monarch":{"xref_id":"0002975"}}}


id: GO:0022411
data:
  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id: PBO:0062819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoclast associated Ig-like receptor","termid":"PBO:0062819"}


id: PBO:0036279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic protein, human CCDC82 ortholog","termid":"PBO:0036279"}


id: GO:0034001
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the exolytic cleavage of disaccharide residues from the non-reducing ends of both polymeric chondroitin sulfates and their oligosaccharide fragments.","definition_xrefs":["EC:4.2.2.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on polysaccharides","termid":"GO:0016837"}],"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:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"chondroitin-sulfate-ABC exolyase activity","secondary_identifiers":["MetaCyc:4.2.2.21-RXN"],"synonyms":[{"name":"ChS ABC lyase II activity","type":"related"},{"name":"ChS ABC lyase activity","type":"broad"},{"name":"chondroitin ABC eliminase activity","type":"broad"},{"name":"chondroitin sulfate ABC exoeliminase activity","type":"related"},{"name":"chondroitin sulfate ABC exolyase activity","type":"related"},{"name":"chondroitin sulfate ABC lyase activity","type":"broad"},{"name":"chondroitinase ABC activity","type":"broad"},{"name":"chondroitinase activity","type":"broad"}],"termid":"GO:0034001"}


id: PBO:0056908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"migration and invasion inhibitory protein","termid":"PBO:0056908"}


id: PBO:0053891
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 1173","termid":"PBO:0053891"}


id: GO:0046524
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + D-fructose 6-phosphate = UDP + sucrose 6-phosphate.","definition_xrefs":["EC:2.4.1.14"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"sucrose-phosphate synthase activity","secondary_identifiers":["MetaCyc:SUCROSE-PHOSPHATE-SYNTHASE-RXN","RHEA:22172"],"synonyms":[{"name":"SPS","type":"related"},{"name":"UDP-glucose-fructose-phosphate glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:D-fructose-6-phosphate 2-alpha-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose-fructose-phosphate glucosyltransferase activity","type":"related"},{"name":"UDPglucose:D-fructose-6-phosphate 2-alpha-D-glucosyltransferase activity","type":"related"},{"name":"sucrose 6-phosphate synthase activity","type":"related"},{"name":"sucrose phosphate synthetase activity","type":"related"},{"name":"sucrose phosphate-uridine diphosphate glucosyltransferase activity","type":"related"},{"name":"sucrosephosphate-UDP glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-fructose phosphate glucosyltransferase activity","type":"related"}],"termid":"GO:0046524"}


id: PBO:0024871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific multicopy membrane protein family 1","termid":"PBO:0024871"}


id: GO:1905825
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of selenocysteine metabolic process.","definition_xrefs":["PMID:19716792","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amino acid metabolic process","termid":"GO:0006521"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"regulates","term_name":"selenocysteine metabolic process","termid":"GO:0016259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"regulation of selenocysteine metabolic process","synonyms":[{"name":"regulation of selenocysteine metabolism","type":"exact"}],"termid":"GO:1905825"}


id: MONDO:0035433
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete calpain-3-related limb-girdle muscular dystrophy D4 (obsolete MONDO:0035433)","secondary_identifiers":["GARD:22272"],"termid":"MONDO:0035433","xrefs":{"Monarch":{"xref_id":"0035433"}}}


id: FYPO:0002921
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 histone ubiquitination is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone modification during vegetative growth","termid":"FYPO:0000330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0002274","FYPO:0001985"],"is_obsolete":false,"name":"abnormal histone ubiquitination during vegetative growth","synonyms":[{"name":"abnormal histone ubiquitination during mitotic cell cycle","type":"related"},{"name":"abnormal histone ubiquitinylation during vegetative growth","type":"exact"},{"name":"abnormal histone ubiquitylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002921"}


id: MONDO:0043373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sensorineural hearing loss which develops suddenly over a period of hours or a few days. It varies in severity from mild to total deafness. Sudden deafness can be due to head trauma, vascular diseases, infections, or can appear without obvious cause or warning.","definition_xrefs":["MESH:D003639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sudden hearing loss disorder","termid":"MONDO:0020677"},{"relation_name":"is_a","term_name":"sensorineural hearing loss disorder","termid":"MONDO:0020678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sudden sensorineural hearing loss","secondary_identifiers":["GARD:12927","MEDGEN:907022","Orphanet:90059","SCTID:715239002","UMLS:C4275242"],"synonyms":[{"name":"acute sensorineural hearing loss by acute acoustic trauma or sudden deafness or surgery induced acoustic trauma","type":"related"},{"name":"deafness, sudden","type":"related"},{"name":"sudden deafness","type":"related"},{"name":"sudden hearing loss","type":"broad"},{"name":"sudden sensorineural hearing loss","type":"exact"}],"termid":"MONDO:0043373","xrefs":{"Monarch":{"xref_id":"0043373"}}}


id: PBO:0045253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal light intermediate chain 1","termid":"PBO:0045253"}


id: PBO:0084912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitotic exit network (MEN) scaffold protein; core component of the SPB outer plaque that functions in astral microtubule organization via Spc72p; scaffold for recruitment of MEN components, such as Cdc15p, Tem1p and the Bfa1p-Bub2p checkpoint complex; phosphorylation by Cdc15p creates a Dbf2p-Mob1p phospho-docking site enabling Cdc15p-dependent complex activation and mitotic exit; acts through the MEN to specify Kar9p-mediated asymmetric SPB inheritance; homologous to mammalian centriolin","termid":"PBO:0084912"}


id: GO:0060126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized structural and/or functional features of a somatotropin secreting cell. A somatotropin secreting cell is an acidophilic cell of the anterior pituitary that produces growth hormone, somatotropin.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"adenohypophysis development","termid":"GO:0021984"}],"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":"somatotropin secreting cell differentiation","synonyms":[{"name":"growth hormone secreting cell differentiation","type":"exact"},{"name":"somatotrope differentiation","type":"related"},{"name":"somatotroph differentiation","type":"related"},{"name":"somatotrophin secreting cell differentiation","type":"exact"},{"name":"somatotropic cell differentiation","type":"related"},{"name":"somatrophic cell differentiation","type":"related"}],"termid":"GO:0060126"}


id: PBO:0004809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homoserine O-acetyltransferase Met6","termid":"PBO:0004809"}


id: MONDO:0019507
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Amelogenesis imperfecta (AI) represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body.","definition_xrefs":["Orphanet:88661"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"dental enamel hypoplasia","termid":"MONDO:0004038"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amelogenesis imperfecta","secondary_identifiers":["ICD9:520.5","MESH:D000567","SCTID:78494001","GARD:5791","NORD:765","DOID:2187","MEDGEN:240","OMIMPS:104500","UMLS:C0002452","CSP:0828-0533","icd11.foundation:1923123066"],"termid":"MONDO:0019507","xrefs":{"Monarch":{"xref_id":"0019507"}}}


id: PBO:0058335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4709","termid":"PBO:0058335"}


id: GO:0102532
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: genkwanin + O2 + reduced [NADPH--hemoprotein reductase] = H2O + oxidized [NADPH--hemoprotein reductase] + scutellarein 7-methyl ether.","definition_xrefs":["RHEA:73427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"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:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"genkwanin 6-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-14748"],"termid":"GO:0102532"}


id: PBO:0031086
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-translation_regulation_phenotype","termid":"PBO:0031086"}


id: PBO:0061399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"natriuretic peptide C","termid":"PBO:0061399"}


id: GO:0097590
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell motility due to the motion of one or more archaeal-type flagella. An archaeal-type flagellum (also called archaellum) is a non-membrane-bounded organelle superficially similar to a bacterial-type flagellum, but having a different molecular structure and lacking a central channel.","definition_xrefs":["GOC:cilia","GOC:krc","Wikipedia:Flagellum#Archaeal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"archaeal or bacterial-type flagellum-dependent cell motility","termid":"GO:0097588"}],"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":"archaeal-type flagellum-dependent cell motility","synonyms":[{"name":"archaeal-type flagellar cell motility","type":"related"}],"termid":"GO:0097590"}


id: MONDO:0015213
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-syndromic visceral malformation (obsolete MONDO:0015213)","secondary_identifiers":["Orphanet:108971"],"synonyms":[{"name":"isolated visceral malformation","type":"related"},{"name":"nonsyndromic visceral malformation","type":"exact"}],"termid":"MONDO:0015213","xrefs":{"Monarch":{"xref_id":"0015213"}}}


id: FYPO:0003359
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to myriocin. Cells stop growing (and may die) at a concentration of myriocin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"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:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0001985","FYPO:0005447","FYPO:0002683","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to myriocin during vegetative growth","synonyms":[{"name":"hypersensitive to myriocin during vegetative growth","type":"exact"},{"name":"sensitive to myriocin during mitotic cell cycle","type":"related"},{"name":"sensitivity to chemicals interfering with lipids during vegetative growth","type":"broad"}],"termid":"FYPO:0003359"}


id: MONDO:0003629
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete uterine corpus serous adenocarcinoma (obsolete MONDO:0003629)","termid":"MONDO:0003629","xrefs":{"Monarch":{"xref_id":"0003629"}}}


id: PBO:0043381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clustered mitochondria homolog pseudogene 11","termid":"PBO:0043381"}


id: GO:0017030
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Stabilization of the structure of beta-galactosidase.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete beta-galactosidase stabilization activity (obsolete GO:0017030)","synonyms":[{"name":"beta-galactosidase stabilization activity","type":"exact"}],"termid":"GO:0017030"}


id: PBO:0087411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit (17 kDa) of TFIID and SAGA complexes; involved in RNA polymerase II transcription initiation and in chromatin modification, similar to histone H3","termid":"PBO:0087411"}


id: MONDO:0011188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An arrhythmogenic right ventricular dysplasia associated with variation in the region 14q12-q22.","definition_xrefs":["PMID:8824801","DOID:0110072"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated arrhythmogenic right ventricular dysplasia","termid":"MONDO:0016342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"arrhythmogenic right ventricular dysplasia 3","secondary_identifiers":["OMIM:602086","MESH:C566584","MEDGEN:356108","UMLS:C1865882"],"synonyms":[{"name":"ARVC3","type":"exact"},{"name":"ARVD3","type":"exact"},{"name":"arrhythmogenic right ventricular cardiomyopathy 3","type":"exact"},{"name":"arrhythmogenic right ventricular dysplasia type 3","type":"exact"},{"name":"arrhythmogenic right ventricular dysplasia, familial, 3","type":"related"},{"name":"familial arrhythmogenic right ventricular dysplasia 3","type":"exact"}],"termid":"MONDO:0011188","xrefs":{"Monarch":{"xref_id":"0011188"}}}


id: PBO:0070987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L19 pseudogene 11","termid":"PBO:0070987"}


id: GO:0071037
data:
  {"annotated_genes":["SJAG_03745","SJAG_03984"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72166,72511],"is_not":false,"summary":null,"term":"GO:0071037"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways occurring in the nucleus and resulting in the breakdown of a small nuclear RNA (snRNA) molecule, initiated by the enzymatic addition of a sequence of adenylyl residues (polyadenylation) at the 3' end the target snRNA.","definition_xrefs":["GOC:dgf","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA catabolic process","termid":"GO:0016076"},{"relation_name":"is_a","term_name":"nuclear RNA surveillance","termid":"GO:0071027"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03745":null,"SJAG_03984":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016073"}],"interesting_parent_ids":["GO:0016073","GO:0008150"],"is_obsolete":false,"name":"nuclear polyadenylation-dependent snRNA catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"nuclear poly(A)-dependent snRNA catabolic process","type":"related"}],"termid":"GO:0071037","terms_by_termid":{"GO:0071037":null}}


id: PR:C6Y4B6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC12G12.17 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4B6"],"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":"non-classical export protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC12G12.17","synonyms":[{"name":"Spom972h-SPAC12G12.17","type":"exact"}],"termid":"PR:C6Y4B6"}


id: PBO:0064687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 23","termid":"PBO:0064687"}


id: PBO:0042037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 90B","termid":"PBO:0042037"}


id: PBO:0056105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysophospholipase 1","termid":"PBO:0056105"}


id: PR:B5BP47
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- vba2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:B5BP47"],"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 transporter C460.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC460.03","synonyms":[{"name":"Spom972h-vba2","type":"exact"}],"termid":"PR:B5BP47"}


id: PBO:0067660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 837, pseudogene","termid":"PBO:0067660"}


id: PBO:0077071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THY1 antisense RNA 1","termid":"PBO:0077071"}


id: GO:0019549
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of glutamate into succinate, that includes the conversion of 4-aminobutyrate to succinate semialdehyde by the pyruvate-dependent gamma aminobutyrate (GABA) transaminase.","definition_xrefs":["GOC:go_curators","GOC:bf","MetaCyc:PWY-4321"],"gene_count":0,"genotype_count":0,"name":"obsolete glutamate catabolic process to succinate via succinate semialdehyde (obsolete GO:0019549)","termid":"GO:0019549"}


id: PBO:0027984
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_elongated_multinucleate_cell_with_abnormal_septum_morphology","termid":"PBO:0027984"}


id: GO:0043249
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for an erythrocyte to attain its fully functional state.","definition_xrefs":["GOC:jl","GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell maturation","termid":"GO:0048469"},{"relation_name":"part_of","term_name":"erythrocyte development","termid":"GO:0048821"}],"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":"erythrocyte maturation","synonyms":[{"name":"RBC maturation","type":"exact"},{"name":"red blood cell maturation","type":"exact"}],"termid":"GO:0043249"}


id: FYPO:0002294
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an elongated germ tube, but does not go on to form a viable dividing cell, and instead lyses.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"vegetative cell lysis","termid":"FYPO:0000647"},{"relation_name":"is_a","term_name":"vegetative cell lysis","termid":"FYPO:0000647"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, with elongated germ tube","termid":"FYPO:0002379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000004","FYPO:0001985","FYPO:0000005"],"is_obsolete":false,"name":"inviable after spore germination with elongated germ tube and cell lysis","synonyms":[{"name":"inviable after spore germination with elongated cell and cell lysis","type":"exact"},{"name":"inviable after spore germination, without cell division, with elongated germ tube and cell lysis","type":"exact"},{"name":"inviable germinated spore with elongated germ tube and cell lysis","type":"exact"},{"name":"lethal after spore germination with elongated germ tube and cell lysis","type":"exact"},{"name":"lysed cell after spore germination with elongated germ tube","type":"exact"}],"termid":"FYPO:0002294"}


id: MONDO:0008567
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid gland papillary carcinoma","termid":"MONDO:0005075"},{"relation_name":"is_a","term_name":"familial nonmedullary thyroid carcinoma","termid":"MONDO:0017896"},{"relation_name":"is_a","term_name":"NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction","termid":"MONDO:0100520"}],"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":"thyroid cancer, nonmedullary, 1","secondary_identifiers":["MEDGEN:1648293","UMLS:C4721429","OMIM:188550"],"synonyms":[{"name":"NMTC1","type":"related"},{"name":"familial nonmedullary thyroid cancer, papillary","type":"related"},{"name":"nonmedullary thyroid carcinoma, papillary","type":"related"},{"name":"papillary carcinoma of thyroid","type":"related"},{"name":"thyroid cancer, nonmedullary, 1","type":"exact"},{"name":"thyroid cancer, nonmedullary, type 1","type":"exact"}],"termid":"MONDO:0008567","xrefs":{"Monarch":{"xref_id":"0008567"}}}


id: GO:0070425
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of a nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway (NLR) pathway.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039532"},{"relation_name":"is_a","term_name":"regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway","termid":"GO:0070424"},{"relation_name":"negatively_regulates","term_name":"nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway","termid":"GO:0035872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway","synonyms":[{"name":"negative regulation of NOD signaling pathway","type":"narrow"},{"name":"negative regulation of nucleotide-binding oligomerization domain containing signaling pathway","type":"narrow"},{"name":"negative regulation of nucleotide-binding oligomerization domain containing signalling pathway","type":"narrow"}],"termid":"GO:0070425"}


id: GO:1902674
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any ciliary basal body that is part of a right posteriolateral flagellum found in Giardia species (trophozoite stage).","definition_xrefs":["ISBN:9780124260207","PMID:5961344","GOC:TermGenie","GOC:giardia","PMID:16607022","GO_REF:0000064"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary basal body","termid":"GO:0036064"},{"relation_name":"part_of","term_name":"right posteriolateral flagellum","termid":"GO:0097557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005575","GO:0015630"],"is_obsolete":false,"name":"right posteriolateral basal body","synonyms":[{"name":"cilial basal body of right posteriolateral cilium","type":"exact"},{"name":"cilial basal body of right posteriolateral flagellum","type":"exact"},{"name":"cilial basal body of right posterolateral cilium","type":"exact"},{"name":"cilial basal body of right posterolateral flagellum","type":"exact"},{"name":"ciliary basal body of right posteriolateral cilium","type":"exact"},{"name":"ciliary basal body of right posteriolateral flagellum","type":"exact"},{"name":"ciliary basal body of right posterolateral cilium","type":"exact"},{"name":"ciliary basal body of right posterolateral flagellum","type":"exact"},{"name":"cilium basal body of right posteriolateral cilium","type":"exact"},{"name":"cilium basal body of right posteriolateral flagellum","type":"exact"},{"name":"cilium basal body of right posterolateral cilium","type":"exact"},{"name":"cilium basal body of right posterolateral flagellum","type":"exact"},{"name":"microtubule basal body of right posteriolateral cilium","type":"exact"},{"name":"microtubule basal body of right posteriolateral flagellum","type":"exact"},{"name":"microtubule basal body of right posterolateral cilium","type":"exact"},{"name":"microtubule basal body of right posterolateral flagellum","type":"exact"},{"name":"right posteriolateral flagellum ciliary basal body","type":"exact"}],"termid":"GO:1902674"}


id: SO:0002175
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An insertion that is the result of base-calling or assembly error.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_alteration_artifact","termid":"SO:0002172"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insertion_artifact","synonyms":[{"name":"insertion artifact","type":"exact"}],"termid":"SO:0002175"}


id: GO:0008180
data:
  {"annotated_genes":["SJAG_03325","SJAG_04948","SJAG_03733","SJAG_04011","SJAG_02764","SJAG_00662","SJAG_00720"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[64888,74022,78270,82323,94831,94953,102058],"is_not":false,"summary":null,"term":"GO:0008180"}]},"cv_name":"cellular_component","definition":"A protein complex that catalyzes the deneddylation of proteins, including the cullin component of SCF ubiquitin E3 ligase; deneddylation increases the activity of cullin family ubiquitin ligases. The signalosome is involved in many regulatory process, including some which control development, in many species; also regulates photomorphogenesis in plants; in many species its subunits are highly similar to those of the proteasome.","definition_xrefs":["PMID:12186635","PMID:14570571","PMID:11019806"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00662":null,"SJAG_00720":null,"SJAG_02764":null,"SJAG_03325":null,"SJAG_03733":null,"SJAG_04011":null,"SJAG_04948":null},"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:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"COP9 signalosome","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"synonyms":[{"name":"COP9 complex","type":"exact"},{"name":"CSN","type":"exact"},{"name":"signalosome","type":"broad"}],"termid":"GO:0008180","terms_by_termid":{"GO:0008180":null}}


id: PBO:0120118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dynamin-related GTPase involved in mitochondrial organization; required for mitochondrial fission and inheritance; self assembles on mitochondrial tubules at incipient division sites; involved in endocytosis; regulates peroxisome fission with Vps1p; role in nuclear envelope remodeling during nucleophagy; mutants in human ortholog DNM1L, which mediates mitochondrial fission, peroxisomal division, autophagy, and mitophagy, are associated with slowly progressive infantile encephalopathy","termid":"PBO:0120118"}


id: MONDO:0013907
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bilateral generalized polymicrogyria is a rare neurological disorder that affects the cerebral cortex (the outer surface of the brain). This is the most widespread form of polymicrogyria and typically affects the entire surface of the brain. Signs and symptoms include severe intellectual disability, problems with movement, and seizures that are difficult or impossible to treat. While the exact cause of bilateral generalized polymicrogyria is not fully understood, it is thought to be due to improper brain development during embryonic growth. Most cases appear to follow an autosomal recessive pattern of inheritance. Treatment is based on the signs and symptoms present in each person.","direct_ancestors":[{"relation_name":"is_a","term_name":"bilateral polymicrogyria","termid":"MONDO:0017091"},{"relation_name":"is_a","term_name":"microcephalic primordial dwarfism due to RTTN deficiency","termid":"MONDO:0018764"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"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":"bilateral generalized polymicrogyria","secondary_identifiers":["MEDGEN:1684616","Orphanet:208447","UMLS:C5139324","GARD:10786","DOID:0080920"],"synonyms":[{"name":"MSSP","type":"related"},{"name":"PMGYS","type":"related"},{"name":"bilateral generalized polymicrogyria","type":"exact"},{"name":"microcephaly, short stature, and polymicrogyria with or without seizures","type":"related"},{"name":"microcephaly, short stature, and polymicrogyria with seizures","type":"exact"},{"name":"polymicrogyria with seizures","type":"related"}],"termid":"MONDO:0013907","xrefs":{"Monarch":{"xref_id":"0013907"}}}


id: GO:0102891
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + 2',3,4,4',6'-pentahydroxychalcone = H+ + 2',3,4,4',6'-pentahydroxychalcone 4'-O-beta-D-glucoside + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 2'4'6'34-pentahydroxychalcone 4'-O-glucosyltransferase activity (obsolete GO:0102891)","termid":"GO:0102891"}


id: PBO:0053682
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 869","termid":"PBO:0053682"}


id: GO:1904872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of telomerase RNA localization to Cajal body.","definition_xrefs":["GO_REF:0000058","PMID:25467444","GOC:BHF","GOC:nc","GOC:BHF_telomere","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of localization","termid":"GO:0032879"},{"relation_name":"regulates","term_name":"telomerase RNA localization to Cajal body","termid":"GO:0090671"}],"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 telomerase RNA localization to Cajal body","termid":"GO:1904872"}


id: PBO:0012309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"middle-meiotic transcription factor Cuf2","termid":"PBO:0012309"}


id: PBO:0042894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement factor D","termid":"PBO:0042894"}


id: GO:0044217
data:
  {"annotated_genes":["SJAG_02392"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[121656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0085039"}]},"cv_name":"cellular_component","definition":"Any constituent part of a secondary organism with which the first organism is interacting.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02392":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"other organism part","references_by_uniquename":{"PMID:30726171":null},"termid":"GO:0044217","terms_by_termid":{"GO:0085039":null}}


id: PBO:0076601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1D22A antisense RNA 1","termid":"PBO:0076601"}


id: GO:0102284
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-threo-sphinganine + NADP = H+ + NADPH + 3-dehydrosphinganinium(1+).","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete L-threo-sphinganine reductase activity (obsolete GO:0102284)","termid":"GO:0102284"}


id: GO:0048927
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a posterior lateral line neuromast support cell. Support cells are non-sensory cells of the neuromast that extend between the sensory hair cells from the basement membrane to the apical surface; they are surrounded by mantle cells.","definition_xrefs":["ISBN:0387968377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuromast support cell differentiation","termid":"GO:0048889"},{"relation_name":"part_of","term_name":"posterior lateral line neuromast development","termid":"GO:0048919"}],"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":"posterior lateral line neuromast support cell differentiation","termid":"GO:0048927"}


id: PBO:0039687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APC regulator of WNT signaling pathway","termid":"PBO:0039687"}


id: PBO:0089108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces japonicus specific protein some similarity to proteases","termid":"PBO:0089108"}


id: PBO:0061415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptide Y","termid":"PBO:0061415"}


id: GO:1901632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of synaptic vesicle membrane organization.","definition_xrefs":["GOC:TermGenie","PMID:22426000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"synaptic vesicle membrane organization","termid":"GO:0048499"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"regulation of synaptic vesicle membrane organization","synonyms":[{"name":"regulation of SLMV biogenesis","type":"narrow"},{"name":"regulation of synaptic vesicle membrane organisation","type":"exact"},{"name":"regulation of synaptic vesicle membrane organization and biogenesis","type":"related"}],"termid":"GO:1901632"}


id: SO:0001062
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