# terms

id: PBO:0027465
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_wall_thickness_at_old_end_during_vegetative_growth","termid":"PBO:0027465"}


id: GO:0046121
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of any one of a family of organic molecules consisting of a purine or pyrimidine base covalently bonded to a sugar deoxyribose (a deoxyribonucleoside).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyribonucleoside metabolic process","termid":"GO:0009120"},{"relation_name":"is_a","term_name":"nucleoside catabolic process","termid":"GO:0009164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"deoxyribonucleoside catabolic process","synonyms":[{"name":"deoxyribonucleoside breakdown","type":"exact"},{"name":"deoxyribonucleoside catabolism","type":"exact"},{"name":"deoxyribonucleoside degradation","type":"exact"}],"termid":"GO:0046121"}


id: GO:0019525
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving keto-D-gluconate, the anion of keto-D-gluconic acid, an aldonic acid derived from glucose.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketogluconate metabolic process","termid":"GO:0019522"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"keto-D-gluconate metabolic process","synonyms":[{"name":"keto-D-gluconate metabolism","type":"exact"}],"termid":"GO:0019525"}


id: GO:0043010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the camera-type eye over time, from its formation to the mature structure. The camera-type eye is an organ of sight that receives light through an aperture and focuses it through a lens, projecting it on a photoreceptor field.","definition_xrefs":["GOC:go_curators","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye development","termid":"GO:0001654"}],"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":"camera-type eye development","secondary_identifiers":["GO:0001747","GO:0031075"],"termid":"GO:0043010"}


id: PBO:0028937
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_5-fluoroorotic_acid","termid":"PBO:0028937"}


id: GO:0009696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving of salicylic acid (2-hydroxybenzoic acid), a derivative of benzoic acid.","definition_xrefs":["ISBN:0943088399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"}],"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":"salicylic acid metabolic process","synonyms":[{"name":"salicylic acid metabolism","type":"exact"}],"termid":"GO:0009696"}


id: PBO:0030154
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_during_vegetative_growth","termid":"PBO:0030154"}


id: MONDO:0012804
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CSRP3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"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":"hypertrophic cardiomyopathy 12","secondary_identifiers":["OMIM:612124","MEDGEN:393755","UMLS:C2677491","DOID:0110318"],"synonyms":[{"name":"CMH12","type":"exact"},{"name":"CSRP3 hypertrophic cardiomyopathy","type":"exact"},{"name":"cardiomyopathy familial hypertrophic 12","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 12","type":"related"},{"name":"cardiomyopathy, familial hypertrophic, type 12","type":"exact"},{"name":"cardiomyopathy, hypertrophic, 12","type":"exact"},{"name":"hypertrophic cardiomyopathy 12","type":"exact"},{"name":"hypertrophic cardiomyopathy caused by mutation in CSRP3","type":"exact"},{"name":"hypertrophic cardiomyopathy type 12","type":"exact"}],"termid":"MONDO:0012804","xrefs":{"Monarch":{"xref_id":"0012804"}}}


id: GO:0019039
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete viral-cell fusion molecule activity (obsolete GO:0019039)","synonyms":[{"name":"viral-cell fusion molecule activity","type":"exact"}],"termid":"GO:0019039"}


id: GO:2000297
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of synapse maturation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of synapse maturation","termid":"GO:0090128"},{"relation_name":"is_a","term_name":"negative regulation of synapse organization","termid":"GO:1905809"},{"relation_name":"negatively_regulates","term_name":"synapse maturation","termid":"GO:0060074"}],"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 synapse maturation","synonyms":[{"name":"negative regulation of synaptic maturation","type":"exact"}],"termid":"GO:2000297"}


id: PBO:0039846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GTPase activating protein 12","termid":"PBO:0039846"}


id: PBO:0030285
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_sulfide_level","termid":"PBO:0030285"}


id: PBO:0067190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 252, pseudogene","termid":"PBO:0067190"}


id: PBO:0003222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S29 (predicted)","termid":"PBO:0003222"}


id: MONDO:0005233
data:
  {"annotated_genes":["SJAG_03689"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011014"}]},"cv_name":"mondo","definition":"A group of at least three distinct histological types of lung cancer, including non-small cell squamous cell carcinoma, adenocarcinoma, and large cell carcinoma. Non-small cell lung carcinomas have a poor response to conventional chemotherapy.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung carcinoma","termid":"MONDO:0005138"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03689":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"non-small cell lung carcinoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["HP:0030358","SCTID:254637007","MESH:D002289","EFO:0003060","ONCOTREE:NSCLC","Orphanet:488201","MEDGEN:40104","DOID:3908","NCIT:C2926","UMLS:C0007131"],"synonyms":[{"name":"NSCLC","type":"exact"},{"name":"NSCLC - non-small cell lung cancer","type":"exact"},{"name":"non-small cell cancer of lung","type":"exact"},{"name":"non-small cell cancer of the lung","type":"exact"},{"name":"non-small cell carcinoma of lung","type":"exact"},{"name":"non-small cell carcinoma of the lung","type":"exact"},{"name":"non-small cell lung cancer","type":"exact"},{"name":"non-small cell lung carcinoma","type":"exact"},{"name":"non-small cell lung carcinoma (disease)","type":"exact"}],"termid":"MONDO:0005233","terms_by_termid":{"MONDO:0011014":null},"xrefs":{"Monarch":{"xref_id":"0005233"}}}


id: PBO:0059441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane spanning 4-domains A12","termid":"PBO:0059441"}


id: GO:0032348
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 resulting in the formation of aldosterone.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of aldosterone metabolic process","termid":"GO:0032345"},{"relation_name":"is_a","term_name":"regulation of aldosterone biosynthetic process","termid":"GO:0032347"},{"relation_name":"is_a","term_name":"negative regulation of steroid hormone biosynthetic process","termid":"GO:0090032"},{"relation_name":"is_a","term_name":"negative regulation of alcohol biosynthetic process","termid":"GO:1902931"},{"relation_name":"negatively_regulates","term_name":"aldosterone biosynthetic process","termid":"GO:0032342"}],"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"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"negative regulation of aldosterone biosynthetic process","synonyms":[{"name":"down regulation of aldosterone biosynthetic process","type":"exact"},{"name":"down-regulation of aldosterone biosynthetic process","type":"exact"},{"name":"downregulation of aldosterone biosynthetic process","type":"exact"},{"name":"inhibition of aldosterone biosynthetic process","type":"narrow"}],"termid":"GO:0032348"}


id: GO:0031958
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A nuclear receptor-mediated signaling pathway initiated by a corticosteroid binding to an intracellular receptor of the nuclear receptor protein family, and ending with regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:11027914","PMID:12606724"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear receptor-mediated steroid hormone signaling pathway","termid":"GO:0030518"}],"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:0008150","GO:0023052"],"is_obsolete":false,"name":"nuclear receptor-mediated corticosteroid signaling pathway","synonyms":[{"name":"corticosteroid receptor signalling pathway","type":"broad"},{"name":"intracellular corticosteroid receptor signaling pathway","type":"exact"}],"termid":"GO:0031958"}


id: PBO:0065005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PR/SET domain 10","termid":"PBO:0065005"}


id: MONDO:0100403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly loss of chromosome 17p. (A cytogenetic abnormality that refers to the loss of all or part of the short arm of chromosome 17 (17p).)","definition_xrefs":["NCIT:C36499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"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:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"acute myeloid leukemia, loss of chromosome 17p","synonyms":[{"name":"AML, del(17p)","type":"exact"},{"name":"AML, loss of chromosome 17p","type":"exact"}],"termid":"MONDO:0100403","xrefs":{"Monarch":{"xref_id":"0100403"}}}


id: MONDO:0013465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any achromatopsia in which the cause of the disease is a mutation in the GNAT2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"achromatopsia","termid":"MONDO:0018852"},{"relation_name":"is_a","term_name":"GNAT2-related retinopathy","termid":"MONDO:0800392"}],"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":"achromatopsia 4","secondary_identifiers":["DOID:0110010","GARD:15723","MEDGEN:330669","MESH:C564206","UMLS:C1841721","OMIM:613856"],"synonyms":[{"name":"ACHM4","type":"exact"},{"name":"GNAT2 achromatopsia","type":"exact"},{"name":"achromatopsia 4","type":"exact"},{"name":"achromatopsia caused by mutation in GNAT2","type":"exact"},{"name":"achromatopsia type 4","type":"exact"}],"termid":"MONDO:0013465","xrefs":{"Monarch":{"xref_id":"0013465"}}}


id: PBO:0030416
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_duplication","termid":"PBO:0030416"}


id: PBO:0064044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 78","termid":"PBO:0064044"}


id: PBO:0091175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N alpha-acetylation related protein Nat2","termid":"PBO:0091175"}


id: PBO:0035997
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_methylation_at_centromere_central_core_during_vegetative_growth","termid":"PBO:0035997"}


id: PR:O94420
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1620.13 gene.","definition_xrefs":["UniProtKB:O94420","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":"phosphatase C1620.13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.13","synonyms":[{"name":"Spom972h-SPCC1620.13","type":"exact"}],"termid":"PR:O94420"}


id: PBO:0041693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CALCRL and TFPI antisense RNA 1","termid":"PBO:0041693"}


id: PBO:0116478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRR/PPR or ankyrin containing protein","termid":"PBO:0116478"}


id: MONDO:0859312
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities","secondary_identifiers":["UMLS:C5774251","MEDGEN:1824024","OMIM:620113"],"termid":"MONDO:0859312","xrefs":{"Monarch":{"xref_id":"0859312"}}}


id: MONDO:0009729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nephropathy-deafness-hyperparathyroidism syndrome is characterized by renal failure without haematuria, parathyroid hyperplasia and sensorineural deafness. It has been described in five children born to consanguineous patents. The mode of inheritance appears to be autosomal recessive.","definition_xrefs":["Orphanet:2668"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nephropathy - deafness - hyperparathyroidism syndrome","secondary_identifiers":["UMLS:C1850553","MESH:C536401","GARD:3940","OMIM:256120","MEDGEN:340569","SCTID:724093004"],"synonyms":[{"name":"Edwards Patton Dilly syndrome","type":"related"},{"name":"Edwards-Patton-Dilly syndrome","type":"exact"},{"name":"nephropathy - deafness - hyperparathyroidism","type":"related"},{"name":"nephropathy, deafness, and hyperparathyroidism","type":"related"}],"termid":"MONDO:0009729","xrefs":{"Monarch":{"xref_id":"0009729"}}}


id: MONDO:0008219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pemphigus is a group of chronic autoimmune skin diseases characterized by blister formations on the outer layer of the skin and the mucous membranes. Three clinical forms have been characterized, of which pemphigus vulgaris is the most frequent (75%).","definition_xrefs":["Orphanet:704"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pemphigus","termid":"MONDO:0006594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"pemphigus vulgaris","secondary_identifiers":["MEDGEN:10621","OMIM:169610","GARD:7355","NANDO:1200229","MESH:C536645","NCIT:C34910","DOID:0060851","SCTID:49420001","EFO:0004719","MedDRA:10052802","UMLS:C0030809","icd11.foundation:278358681","ICD10CM:L10.0"],"synonyms":[{"name":"familial pemphigus vulgaris","type":"exact"},{"name":"pemphigus vulgaris, familial","type":"related"}],"termid":"MONDO:0008219","xrefs":{"Monarch":{"xref_id":"0008219"}}}


id: MONDO:0006484
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplastic ductal proliferative lesion of the breast characterized by the formation of secondary lumens and prominent intraductal proliferation of a heterogeneous cellular population that may include epithelial cells, myoepithelial cells, or metaplastic apocrine cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast intraductal proliferative lesion","termid":"MONDO:0004007"},{"relation_name":"is_a","term_name":"hyperplasia","termid":"MONDO:0005043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"usual ductal breast hyperplasia","secondary_identifiers":["MEDGEN:759542","EFO:1000612","NCIT:C27941","UMLS:C3532429","SCTID:472905007","ICD9:611.89"],"synonyms":[{"name":"UDH","type":"exact"},{"name":"ductal breast hyperplasia of usual type","type":"exact"},{"name":"ordinary intraductal breast hyperplasia","type":"exact"}],"termid":"MONDO:0006484","xrefs":{"Monarch":{"xref_id":"0006484"}}}


id: PBO:0038414
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_o_transports_or_maintains_localization_of","termid":"PBO:0038414"}


id: GO:0046095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of deoxyinosine, hypoxanthine deoxyriboside.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyinosine metabolic process","termid":"GO:0046094"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside biosynthetic process","termid":"GO:0046123"}],"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:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"deoxyinosine biosynthetic process","synonyms":[{"name":"deoxyinosine anabolism","type":"exact"},{"name":"deoxyinosine biosynthesis","type":"exact"},{"name":"deoxyinosine formation","type":"exact"},{"name":"deoxyinosine synthesis","type":"exact"}],"termid":"GO:0046095"}


id: MONDO:0013322
data:
  {"annotated_genes":["SJAG_03657"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89015],"is_not":false,"summary":null,"term":"MONDO:0013322"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"benign adult familial myoclonic epilepsy","termid":"MONDO:0019448"},{"relation_name":"is_a","term_name":"epilepsy, familial adult myoclonic","termid":"MONDO:0000160"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03657":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"epilepsy, familial adult myoclonic, 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:462210","GARD:18084","MESH:C567098","DOID:0111695","OMIM:613608","UMLS:C3150860"],"synonyms":[{"name":"FAME3","type":"exact"},{"name":"cortical myoclonic tremor with epilepsy, familial, 3","type":"related"},{"name":"epilepsy, familial ADULT myoclonic, 3","type":"related"}],"termid":"MONDO:0013322","terms_by_termid":{"MONDO:0013322":null},"xrefs":{"Monarch":{"xref_id":"0013322"}}}


id: PBO:0067760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 60","termid":"PBO:0067760"}


id: PBO:0088692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"importin alpha family nuclear import signal receptor adaptor Imp1","termid":"PBO:0088692"}


id: MONDO:0008749
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pseudohypoparathyroidism type 2 (PHP2) is a type of pseudohypoparathyroidism (PHP) characterized by resistance to parathyroid hormone (PTH), which manifests with hypocalcemia, hyperphosphatemia and elevated PTH levels, absence of Albright's hereditary osteodystrophy (AHO), and normal expression of the Gs protein with a normal urinary cAMP response.","definition_xrefs":["Orphanet:94090"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudohypoparathyroidism","termid":"MONDO:0019992"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005240"],"is_obsolete":false,"name":"pseudohypoparathyroidism type 2","secondary_identifiers":["NANDO:1201078","icd11.foundation:1650158822","MESH:C548077","UMLS:C2932717","ICD9:275.49","OMIM:203330","SCTID:42183005","GARD:10682","MEDGEN:444371"],"synonyms":[{"name":"PHP II","type":"related"},{"name":"PHP2","type":"related"},{"name":"Php 2","type":"related"},{"name":"pseudohypoparathyroidism, type II","type":"related"}],"termid":"MONDO:0008749","xrefs":{"Monarch":{"xref_id":"0008749"}}}


id: MONDO:0012721
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the KCTD7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"},{"relation_name":"is_a","term_name":"neuronal ceroid lipofuscinosis","termid":"MONDO:0016295"},{"relation_name":"is_a","term_name":"progressive myoclonus epilepsy","termid":"MONDO:0020074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0024322","MONDO:0005027","MONDO:0002561","MONDO:0002320","MONDO:0005559","MONDO:0005066"],"is_obsolete":false,"name":"progressive myoclonic epilepsy type 3","secondary_identifiers":["SCTID:783064000","DOID:0111446","icd11.foundation:383417276","MEDGEN:388595","OMIM:611726","Orphanet:263516","GARD:2167","UMLS:C2673257","MESH:C567095"],"synonyms":[{"name":"EPM 3","type":"related"},{"name":"EPM3","type":"exact"},{"name":"KCTD7 progressive myoclonic epilepsy","type":"exact"},{"name":"PME type 3","type":"exact"},{"name":"ceroid lipofuscinosis, neuronal, 14","type":"related"},{"name":"epilepsy progressive myoclonic type 3","type":"related"},{"name":"epilepsy, progressive myoclonic 3, with or without intracellular inclusions","type":"exact"},{"name":"epilepsy, progressive myoclonic, 3, with or without intracellular inclusions","type":"related"},{"name":"progressive myoclonic epilepsy 3","type":"related"},{"name":"progressive myoclonic epilepsy caused by mutation in KCTD7","type":"exact"},{"name":"progressive myoclonic epilepsy due to KCTD7 deficiency","type":"exact"},{"name":"progressive myoclonic epilepsy type 3","type":"exact"},{"name":"progressive myoclonus epilepsy type 3","type":"exact"}],"termid":"MONDO:0012721","xrefs":{"Monarch":{"xref_id":"0012721"}}}


id: PR:Q10199
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An F-BAR domain only protein 2 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":"septation protein imp2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC11C11.02","secondary_identifiers":["UniProtKB:Q10199"],"synonyms":[{"name":"SPBC11C11.02","type":"related"},{"name":"Spom972h-FCHO2","type":"exact"}],"termid":"PR:Q10199"}


id: PBO:0054706
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 2115","termid":"PBO:0054706"}


id: GO:0160210
data:
  {"annotated_genes":["SJAG_04305"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103790],"is_not":false,"summary":null,"term":"GO:0160210"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-serine + succinyl-CoA = CoA + O-succinyl-L-serine.","definition_xrefs":["RHEA:52820","PMID:28581482"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-succinyltransferase activity","termid":"GO:0016750"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04305":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016746","GO:0003824"],"is_obsolete":false,"name":"L-serine O-succinyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0160210","terms_by_termid":{"GO:0160210":null}}


id: MONDO:0025622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1","secondary_identifiers":["OMIM:500013","UMLS:C5435765","MEDGEN:1731194"],"synonyms":[{"name":"CMTMA1","type":"exact"}],"termid":"MONDO:0025622","xrefs":{"Monarch":{"xref_id":"0025622"}}}


id: PBO:0076318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptopodin 2","termid":"PBO:0076318"}


id: PBO:0076778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TEA domain transcription factor 1","termid":"PBO:0076778"}


id: PBO:0048471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"germ cell nuclear acidic peptidase","termid":"PBO:0048471"}


id: PBO:0038825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 32","termid":"PBO:0038825"}


id: PBO:0034318
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-receives_input_from","termid":"PBO:0034318"}


id: MONDO:0020355
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coloboma","termid":"MONDO:0001476"}],"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":"coloboma of eye lens","secondary_identifiers":["icd11.foundation:1368271881","GARD:1433","MEDGEN:451043","Orphanet:98943","UMLS:C0344516"],"termid":"MONDO:0020355","xrefs":{"Monarch":{"xref_id":"0020355"}}}


id: PBO:0046539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group E member 2","termid":"PBO:0046539"}


id: MONDO:0012632
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Alzheimer disease 15 (obsolete MONDO:0012632)","termid":"MONDO:0012632","xrefs":{"Monarch":{"xref_id":"0012632"}}}


id: GO:0010015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of roots are generated and organized. The root is the usually underground part of a seed plant body that originates from the hypocotyl, functions as an organ of absorption, aeration, and food storage or as a means of anchorage and support.","definition_xrefs":["GOC:sm","ISBN:0877797099"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant organ morphogenesis","termid":"GO:1905392"},{"relation_name":"part_of","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":"root morphogenesis","termid":"GO:0010015"}


id: GO:0160224
data:
  {"annotated_genes":["SJAG_00459"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111232],"is_not":false,"summary":null,"term":"GO:0160224"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a 5-methoxy-2-methyl-3-(all-trans-polyprenyl)benzoquinone + NADH + O2 = a 3-demethylubiquinone + NAD+ + H2O.","definition_xrefs":["PMID:38425362","RHEA:81211","PMID:23445365"],"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":1,"genes_by_uniquename":{"SJAG_00459":null},"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:0016491","GO:0003674"],"is_obsolete":false,"name":"3-demethoxyubiquinone 3-hydroxylase (NADH) activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"5-methoxy-2-methyl-3-(all-trans-polyprenyl)benzoquinone,NADH:oxygen oxidoreductase (5-hydroxylating) activity","type":"exact"}],"termid":"GO:0160224","terms_by_termid":{"GO:0160224":null}}


id: GO:0004096
data:
  {"annotated_genes":["SJAG_04823"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72744],"is_not":false,"summary":null,"term":"GO:0004096"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 hydrogen peroxide = O2 + 2 H2O.","definition_xrefs":["EC:1.11.1.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxidase activity","termid":"GO:0004601"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04823":null},"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:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"catalase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["UM-BBD_enzymeID:r1335","Reactome:R-HSA-1222704","RHEA:20309","GO:0016952","MetaCyc:CATAL-RXN","GO:0016953","Reactome:R-HSA-76031"],"synonyms":[{"name":"CAT","type":"related"},{"name":"bacterial catalase-peroxidase activity","type":"narrow"},{"name":"caperase activity","type":"related"},{"name":"catalase reaction","type":"exact"},{"name":"catalase-peroxidase activity","type":"related"},{"name":"equilase activity","type":"related"},{"name":"haem catalase activity","type":"narrow"},{"name":"heme catalase activity","type":"narrow"},{"name":"hydrogen-peroxide:hydrogen-peroxide oxidoreductase activity","type":"related"},{"name":"manganese catalase activity","type":"narrow"},{"name":"optidase activity","type":"related"}],"termid":"GO:0004096","terms_by_termid":{"GO:0004096":null}}


id: PBO:0069858
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1145, pseudogene","termid":"PBO:0069858"}


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: PBO:0074236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 49 member 3","termid":"PBO:0074236"}


id: PBO:0116393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mug2/mug135/meu2 family protein","termid":"PBO:0116393"}


id: GO:0006653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving any 1,2-diacyl-sn-glycero-3-phosphocholine, the compounds most commonly designated lecithin.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylcholine metabolic process","termid":"GO:0046470"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"1,2-diacyl-sn-glycero-3-phosphocholine metabolic process","synonyms":[{"name":"1,2-diacyl-sn-glycero-3-phosphocholine metabolism","type":"exact"},{"name":"lecithin metabolic process","type":"broad"}],"termid":"GO:0006653"}


id: GO:0051046
data:
  {"annotated_genes":["SJAG_00661","SJAG_02366","SJAG_03763","SJAG_04509"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045921"},{"annotations":[61608,89709,100269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017157"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the controlled release of a substance from a cell or a tissue.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"secretion","termid":"GO:0046903"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00661":null,"SJAG_02366":null,"SJAG_03763":null,"SJAG_04509":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of secretion","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0051046","terms_by_termid":{"GO:0017157":null,"GO:0045921":null}}


id: PBO:0043329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC like kinase 4","termid":"PBO:0043329"}


id: PBO:0076812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TEN1-CDK3 readthrough (NMD candidate)","termid":"PBO:0076812"}


id: MONDO:0009975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An antiquated term that refers to a non-Hodgkin lymphoma composed of diffuse infiltrates of large, often anaplastic lymphocytes.","definition_xrefs":["NCIT:C27824"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphatic system cancer","termid":"MONDO:0000612"},{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"},{"relation_name":"is_a","term_name":"dendritic cell tumor","termid":"MONDO:0020082"}],"gene_count":0,"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:0004992"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"reticulum cell sarcoma","secondary_identifiers":["UMLS:C0024302","Orphanet:86900","GARD:16765","EFO:0005287","MedDRA:10038804","MESH:D054739","ICD9:200.00","MEDGEN:44224","DOID:8538","ICD9:200.0","MESH:D008228","SCTID:373168002","ICD9:200.7","OMIM:267730"],"synonyms":[{"name":"Reticulum cell sarcoma","type":"exact"},{"name":"histiocytic lymphoma","type":"exact"},{"name":"interdigitating cell sarcoma","type":"exact"},{"name":"large-cell Lymphomas","type":"exact"},{"name":"reticular cell sarcoma","type":"exact"},{"name":"reticulosarcoma","type":"exact"},{"name":"reticulum cell sarcoma","type":"exact"},{"name":"sarcoma of reticular cell","type":"exact"}],"termid":"MONDO:0009975","xrefs":{"Monarch":{"xref_id":"0009975"}}}


id: GO:0019420
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reduction of sulfate to hydrogen sulfide, which acts as a terminal electron acceptor. Sulfate is activated to adenosine-phosphosulfate (APS) which is then reduced to sulfite, which is in turn reduced to hydrogen sulfide.","definition_xrefs":["PMID:26680199","PMID:25400653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfate assimilation","termid":"GO:0000103"},{"relation_name":"is_a","term_name":"anaerobic respiration","termid":"GO:0009061"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006091","GO:0006790","GO:0008150"],"is_obsolete":false,"name":"dissimilatory sulfate reduction","secondary_identifiers":["Wikipedia:Sulfate-reducing_microorganism","MetaCyc:DISSULFRED-PWY"],"synonyms":[{"name":"dissimilatory sulphate reduction","type":"exact"}],"termid":"GO:0019420"}


id: PBO:0002980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino acid permease (predicted)","termid":"PBO:0002980"}


id: PBO:0075163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide C pseudogene 19","termid":"PBO:0075163"}


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:0700092","MONDO:0002320"],"is_obsolete":false,"name":"X-linked adrenal hypoplasia congenita","secondary_identifiers":["GARD:555","DOID:0080156","MEDGEN:87442","NANDO:2200357","NANDO:1200403","Orphanet:95702","SCTID:93235007","OMIM:300200","UMLS:C0342482"],"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: GO:0018077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of one or more iodine atoms to an amino acid residue in a protein.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete protein iodination (obsolete GO:0018077)","synonyms":[{"name":"protein amino acid iodination","type":"exact"}],"termid":"GO:0018077"}


id: PBO:0042190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin D2","termid":"PBO:0042190"}


id: PBO:0057521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 639","termid":"PBO:0057521"}


id: PBO:0078367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 11-1","termid":"PBO:0078367"}


id: PBO:0085655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in mitochondrial functions and stress response; overexpression suppresses growth defects of hap2, hap3, and hap4 mutants; MBR1 has a paralog, ISF1, that arose from the whole genome duplication","termid":"PBO:0085655"}


id: PBO:0001035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human 4F5S homolog","termid":"PBO:0001035"}


id: GO:0034361
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A triglyceride-rich lipoprotein particle that is typically composed of APOB100, APOE and APOCs and has a density of about 1.006 g/ml and a diameter of between 20-80 nm. It is found in blood and transports endogenous products (newly synthesized cholesterol and triglycerides) from the liver.","definition_xrefs":["GOC:expert_pt","GOC:BHF","GOC:rl","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triglyceride-rich plasma lipoprotein particle","termid":"GO:0034385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005575","GO:0005576","GO:0032991"],"is_obsolete":false,"name":"very-low-density lipoprotein particle","synonyms":[{"name":"VLDL complex","type":"exact"},{"name":"VLDL particle","type":"exact"},{"name":"very-low-density lipoprotein complex","type":"exact"}],"termid":"GO:0034361"}


id: MONDO:0018465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Insulin autoimmune syndrome is a rare condition that causes low blood sugar (hypoglycemia). This occurs because the body begins to make a specific kind of protein called antibodies to attack insulin. Insulin is a naturally occurring hormone that is responsible for keeping blood sugar at a normal level. When blood sugar levels get too high, insulin helps to store the sugar for future use. People affected by insulin autoimmune syndrome have antibodies that attack insulin, causing it to work too hard and the level of blood sugar to become too low. Insulin autoimmune syndrome most often begins during adulthood.","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of endocrine system","termid":"MONDO:0000569"},{"relation_name":"is_a","term_name":"hyperinsulinemic hypoglycemia","termid":"MONDO:0005803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0005046"],"is_obsolete":false,"name":"insulin autoimmune syndrome","secondary_identifiers":["UMLS:C0854359","GARD:10808","DOID:0040100","ICD9:279.49","Orphanet:411593","SCTID:408539000","MEDGEN:678528"],"synonyms":[{"name":"Hirata disease","type":"exact"},{"name":"insulin autoimmune hypoglycemia","type":"related"}],"termid":"MONDO:0018465","xrefs":{"Monarch":{"xref_id":"0018465"}}}


id: GO:0031086
data:
  {"annotated_genes":["SJAG_02370","SJAG_04640","SJAG_03023"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77801,80580],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031087"},{"annotations":[93510],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036450"}]},"cv_name":"biological_process","definition":"A pathway of degradation of nuclear-transcribed mRNAs that proceeds through a series of steps that is independent of deadenylation, but requires decapping followed by transcript decay, and that can regulate mRNA stability.","definition_xrefs":["PMID:15225544","GOC:krc","PMID:15225542"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear-transcribed mRNA catabolic process","termid":"GO:0000956"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02370":null,"SJAG_03023":null,"SJAG_04640":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"nuclear-transcribed mRNA catabolic process, deadenylation-independent decay","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"deadenylation-independent mRNA decay","type":"exact"},{"name":"deadenylylation-independent mRNA decay","type":"exact"},{"name":"mRNA breakdown, deadenylation-independent decay","type":"exact"},{"name":"mRNA catabolic process, deadenylation-independent","type":"exact"},{"name":"mRNA catabolic process, deadenylylation-independent","type":"exact"},{"name":"mRNA catabolism, deadenylation-independent","type":"exact"},{"name":"mRNA catabolism, deadenylation-independent decay","type":"exact"},{"name":"mRNA catabolism, deadenylylation-independent","type":"exact"},{"name":"mRNA degradation, deadenylation-independent decay","type":"exact"},{"name":"nuclear mRNA catabolic process, deadenylation-independent decay","type":"exact"}],"termid":"GO:0031086","terms_by_termid":{"GO:0031087":null,"GO:0036450":null}}


id: GO:0033289
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A microtubule located such that it threads through the conoid and projects through the polar ring.","definition_xrefs":["PMID:16518471","GOC:mah","PMID:11901169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule","termid":"GO:0005874"},{"relation_name":"part_of","term_name":"apical complex","termid":"GO:0020007"}],"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:0015630","GO:0005575"],"is_obsolete":false,"name":"intraconoid microtubule","termid":"GO:0033289"}


id: PBO:0067014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 23, pseudogene","termid":"PBO:0067014"}


id: PBO:0050142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 2","termid":"PBO:0050142"}


id: MONDO:0002219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the paraurethral gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vulvar neoplasm","termid":"MONDO:0021049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paraurethral gland neoplasm","secondary_identifiers":["DOID:2139","MEDGEN:574628","UMLS:C0341766","SCTID:126884005","ICD9:239.5"],"synonyms":[{"name":"neoplasm of paraurethral gland","type":"exact"},{"name":"neoplasm of paraurethral glands","type":"exact"},{"name":"paraurethral gland neoplasm (disease)","type":"exact"},{"name":"paraurethral gland tumor","type":"exact"},{"name":"paraurethral gland tumour","type":"exact"},{"name":"tumor of paraurethral gland","type":"exact"},{"name":"tumor of the paraurethral gland","type":"exact"},{"name":"tumour of paraurethral gland","type":"exact"},{"name":"tumour of the paraurethral gland","type":"exact"}],"termid":"MONDO:0002219","xrefs":{"Monarch":{"xref_id":"0002219"}}}


id: MOD:01603
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to 2x(15)N labeled L-lysine.","definition_xrefs":["PubMed:18688235","URL:http://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=609021|ALDRICH&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC&lang=en_US0.000000E+000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(15)N labeled residue","termid":"MOD:00843"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2x(15)N labeled L-lysine","termid":"MOD:01603"}


id: PBO:0108582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snoRNA primary transcript for snR46","termid":"PBO:0108582"}


id: GO:0003774
data:
  {"annotated_genes":["SJAG_04001","SJAG_03703","SJAG_01613","SJAG_03011","SJAG_01546","SJAG_00930","SJAG_02286","SJAG_02848","SJAG_00332","SJAG_02336","SJAG_02384","SJAG_02431","SJAG_00851","SJAG_00773","SJAG_00042","SJAG_00938","SJAG_04745","SJAG_01297","SJAG_00031"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061791"},{"annotations":[101849,104671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990606"},{"annotations":[72849,78427,81372,71912,76118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000146"},{"annotations":[62031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003777"},{"annotations":[59405,98651,67381,96638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008569"},{"annotations":[63003,77578,77705,79583,80622,105452,105653],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008574"}]},"cv_name":"molecular_function","definition":"Generation of force resulting in movement, for example along a microfilament or microtubule, or in torque resulting in membrane scission or rotation of a flagellum. The energy required is obtained either from the hydrolysis of a nucleoside triphosphate or by an electrochemical proton gradient (proton-motive force).","definition_xrefs":["GOC:vw","GOC:mah","PMID:11242086","PMID:29716949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00031":null,"SJAG_00042":null,"SJAG_00332":null,"SJAG_00773":null,"SJAG_00851":null,"SJAG_00930":null,"SJAG_00938":null,"SJAG_01297":null,"SJAG_01546":null,"SJAG_01613":null,"SJAG_02286":null,"SJAG_02336":null,"SJAG_02384":null,"SJAG_02431":null,"SJAG_02848":null,"SJAG_03011":null,"SJAG_03703":null,"SJAG_04001":null,"SJAG_04745":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"cytoskeletal motor activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-1861595"],"synonyms":[{"name":"motor activity","type":"broad"}],"termid":"GO:0003774","terms_by_termid":{"GO:0000146":null,"GO:0003777":null,"GO:0008569":null,"GO:0008574":null,"GO:0061791":null,"GO:1990606":null}}


id: GO:0047261
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: estradiol-17alpha 3-D-glucuronoside + UDP-N-acetyl-alpha-D-glucosamine = 17alpha-(N-acetyl-D-glucosaminyl)-estradiol 3-D-glucuronoside + H+ + UDP.","definition_xrefs":["EC:2.4.1.39","RHEA:14153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016757","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"steroid N-acetylglucosaminyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.39-RXN","KEGG_REACTION:R04451"],"synonyms":[{"name":"UDP-N-acetyl-D-glucosamine:estradiol-17alpha-3-D-glucuronoside 17alpha-N-acetylglucosaminyltransferase activity","type":"related"},{"name":"hydroxy steroid acetylglucosaminyltransferase activity","type":"related"},{"name":"steroid acetylglucosaminyltransferase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-steroid acetylglucosaminyltransferase activity","type":"related"}],"termid":"GO:0047261"}


id: PBO:0001024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP protein Utp14 (predicted)","termid":"PBO:0001024"}


id: PBO:0049120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPR107 adjacent cis regulating lncRNA","termid":"PBO:0049120"}


id: MONDO:0002290
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that affects the clitoris.","definition_xrefs":["NCIT:C3557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vulva cancer","termid":"MONDO:0001528"},{"relation_name":"is_a","term_name":"clitoris neoplasm","termid":"MONDO:0024877"}],"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":"clitoris cancer","secondary_identifiers":["UMLS:C0153589","DOID:2401","ICD9:184.3","MEDGEN:56312","SCTID:371979001"],"synonyms":[{"name":"cancer of clitoris","type":"exact"},{"name":"carcinoma of clitoris","type":"narrow"},{"name":"clitoral Ca","type":"exact"},{"name":"clitoris cancer","type":"exact"},{"name":"malignant clitoral neoplasm","type":"exact"},{"name":"malignant clitoral tumor","type":"exact"},{"name":"malignant clitoral tumour","type":"exact"},{"name":"malignant clitoris neoplasm","type":"exact"},{"name":"malignant clitoris tumor","type":"exact"},{"name":"malignant clitoris tumour","type":"exact"},{"name":"malignant neoplasm of clitoris","type":"exact"},{"name":"malignant neoplasm of the clitoris","type":"exact"},{"name":"malignant tumor of clitoris","type":"exact"},{"name":"malignant tumor of the clitoris","type":"exact"},{"name":"malignant tumour of clitoris","type":"exact"},{"name":"malignant tumour of the clitoris","type":"exact"}],"termid":"MONDO:0002290","xrefs":{"Monarch":{"xref_id":"0002290"}}}


id: GO:0009218
data:
  {"annotated_genes":["SJAG_04665","SJAG_03164","SJAG_00885","SJAG_00964","SJAG_03708","SJAG_00779","SJAG_05024","SJAG_04713","SJAG_02887","SJAG_00197","SJAG_03676","SJAG_04709","SJAG_00694","SJAG_00533","SJAG_04354","SJAG_00444"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[64132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044210"},{"annotations":[59762,57220,61627,59387,62632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044205"},{"annotations":[82219],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046705"},{"annotations":[109185,94277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046704"},{"annotations":[69582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009224"},{"annotations":[65593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006241"},{"annotations":[78223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046036"},{"annotations":[94812,69584],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044211"},{"annotations":[82218],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006225"},{"annotations":[78222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006256"},{"annotations":[93809,89267,94813,90265,69583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044206"},{"annotations":[65592],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006228"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving a pyrimidine ribonucleotide, a compound consisting of nucleoside (a pyrimidine base linked to a ribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleotide metabolic process","termid":"GO:0006220"},{"relation_name":"is_a","term_name":"ribonucleotide metabolic process","termid":"GO:0009259"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00444":null,"SJAG_00533":null,"SJAG_00694":null,"SJAG_00779":null,"SJAG_00885":null,"SJAG_00964":null,"SJAG_02887":null,"SJAG_03164":null,"SJAG_03676":null,"SJAG_03708":null,"SJAG_04354":null,"SJAG_04665":null,"SJAG_04709":null,"SJAG_04713":null,"SJAG_05024":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"pyrimidine ribonucleotide metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"pyrimidine ribonucleotide metabolism","type":"exact"}],"termid":"GO:0009218","terms_by_termid":{"GO:0006225":null,"GO:0006228":null,"GO:0006241":null,"GO:0006256":null,"GO:0009224":null,"GO:0044205":null,"GO:0044206":null,"GO:0044210":null,"GO:0044211":null,"GO:0046036":null,"GO:0046704":null,"GO:0046705":null}}


id: PATO:0002444
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A composition quality inhering in a bearer by virtue of the bearer's being composed of or possessing inorganic material.","definition_xrefs":["PATOC:WC"],"direct_ancestors":[{"relation_name":"is_a","term_name":"composition","termid":"PATO:0000025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mineralized","termid":"PATO:0002444"}


id: MONDO:0600029
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Decreased lung volume and inadequate ventilation due to parenchymal lung disorders (e.g., interstitial pulmonary fibrosis) or extrapulmonary disorders (e.g., scoliosis). Patients present with shortness of breath and cough.","definition_xrefs":["NCIT:C91762"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung disorder","termid":"MONDO:0005275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restrictive pulmonary disease","secondary_identifiers":["UMLS:C0085581","MEDGEN:43209","SCTID:36485005"],"synonyms":[{"name":"Restrictive lung disease (disorder)","type":"exact"},{"name":"restrictive lung disease","type":"exact"}],"termid":"MONDO:0600029","xrefs":{"Monarch":{"xref_id":"0600029"}}}


id: PBO:0056931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial intermediate peptidase pseudogene 3","termid":"PBO:0056931"}


id: GO:0102627
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: O2 + parthenolide + reduced [NADPH--hemoprotein reductase] = 3beta-hydroxyparthenolide + H+ + H2O + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:61328"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"parthenolide 3beta-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-15532"],"termid":"GO:0102627"}


id: PBO:0077506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 223","termid":"PBO:0077506"}


id: MONDO:1010802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Brachydactyly that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brachydactyly, non-human animal","termid":"MONDO:1010156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly, pig","secondary_identifiers":["OMIA:000146-9823"],"termid":"MONDO:1010802","xrefs":{"Monarch":{"xref_id":"1010802"}}}


id: MOD:00120
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links an L-cysteine residue and an L-serine residue by a thioether bond to form meso-lanthionine.","definition_xrefs":["RESID:AA0111","PubMed:15023056","PubMed:3769923"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"lanthionine","termid":"MOD:01841"},{"relation_name":"is_a","term_name":"crosslinked L-serine residue","termid":"MOD:02055"}],"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":"meso-lanthionine","synonyms":[{"name":"(2R,2'S)-3,3'-sulfanediylbis(2-aminopropanoic acid)","type":"exact"},{"name":"(2R,2'S)-3,3'-thiobis-(2-aminopropanoic acid)","type":"exact"},{"name":"(2R,6S)-2,6-diamino-4-thiaheptanedioic acid","type":"exact"},{"name":"(2R,6S)-meso-lanthionine","type":"exact"},{"name":"(2S)-2-amino-3-[[(2R)-2-amino-2-carboxyethyl]sulfanyl]propanoic acid","type":"exact"},{"name":"(2S,6R)-meso-lanthionine","type":"related"},{"name":"(R)-S-(2-amino-2-carboxyethyl)-D-cysteine","type":"exact"},{"name":"(R,S)-bis(2-amino-2-carboxyethyl)sulfide","type":"exact"},{"name":"3,3'-thiobis-meso-alanine","type":"exact"},{"name":"CROSSLNK Lanthionine (Cys-Ser)","type":"exact"},{"name":"CROSSLNK Lanthionine (Ser-Cys)","type":"exact"},{"name":"XLNK-SCys-(D)3Dha","type":"exact"},{"name":"cysteine-3-D-alanine thioether","type":"exact"},{"name":"meso-lanthionine","type":"exact"}],"termid":"MOD:00120"}


id: GO:0071236
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 antibiotic stimulus. An antibiotic is a chemical substance produced by a microorganism which has the capacity to inhibit the growth of or to kill other microorganisms.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to antibiotic","termid":"GO:0046677"},{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"}],"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 antibiotic","termid":"GO:0071236"}


id: GO:1900720
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of uterine smooth muscle relaxation.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of uterine smooth muscle relaxation","termid":"GO:1900719"},{"relation_name":"is_a","term_name":"negative regulation of relaxation of smooth muscle","termid":"GO:1901081"},{"relation_name":"negatively_regulates","term_name":"uterine smooth muscle relaxation","termid":"GO:0044558"}],"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 uterine smooth muscle relaxation","synonyms":[{"name":"down regulation of smooth muscle relaxation of the uterus","type":"exact"},{"name":"down regulation of uterine smooth muscle relaxation","type":"exact"},{"name":"down-regulation of smooth muscle relaxation of the uterus","type":"exact"},{"name":"down-regulation of uterine smooth muscle relaxation","type":"exact"},{"name":"downregulation of smooth muscle relaxation of the uterus","type":"exact"},{"name":"downregulation of uterine smooth muscle relaxation","type":"exact"},{"name":"inhibition of smooth muscle relaxation of the uterus","type":"exact"},{"name":"inhibition of uterine smooth muscle relaxation","type":"narrow"},{"name":"negative regulation of smooth muscle relaxation of the uterus","type":"exact"}],"termid":"GO:1900720"}


id: GO:0061347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of a Wnt protein to a receptor on the surface of the target cell where activated receptors signal via downstream effectors including C-Jun N-terminal kinase (JNK) to modulate cytoskeletal elements and control cell polarity that contributes to the shaping of the outflow tract.","definition_xrefs":["GOC:dph","GOC:mtg_heart","PMID:19056682"],"gene_count":0,"genotype_count":0,"name":"obsolete planar cell polarity pathway involved in outflow tract morphogenesis (obsolete GO:0061347)","termid":"GO:0061347"}


id: PBO:0052909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 13-1","termid":"PBO:0052909"}


id: GO:0072400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about DNA integrity is received and converted into a molecular signal, contributing to a mitotic DNA integrity checkpoint.","definition_xrefs":["GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in mitotic DNA integrity checkpoint (obsolete GO:0072400)","synonyms":[{"name":"DNA integrity checkpoint sensor mechanism","type":"related"},{"name":"DNA integrity checkpoint sensor process","type":"related"},{"name":"detection of stimulus involved in mitotic G2/M transition decatenation checkpoint","type":"related"},{"name":"mitotic G2/M transition decatenation checkpoint sensor mechanism","type":"related"},{"name":"mitotic G2/M transition decatenation checkpoint sensor process","type":"related"},{"name":"sensing involved in DNA integrity checkpoint","type":"related"},{"name":"sensing involved in mitotic G2/M transition decatenation checkpoint","type":"related"}],"termid":"GO:0072400"}


id: PR:O60060
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A carbamoyl-phosphate synthase small chain that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03990"],"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":"carbamoyl-phosphate synthase arginine-specific small chain (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC56F2.09c","secondary_identifiers":["UniProtKB:O60060"],"synonyms":[{"name":"CPS-A (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-carA","type":"exact"},{"name":"arginine-specific carbamoyl-phosphate synthetase, glutamine chain (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60060"}


id: PBO:0075208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide G pseudogene 20","termid":"PBO:0075208"}


id: GO:0001990
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which hormones modulate the force with which blood passes through the circulatory system. A hormone is one of a group of substances formed in very small amounts in one specialized organ or group of cells and carried (sometimes in the bloodstream) to another organ or group of cells, in the same organism, upon which they have a specific regulatory action.","definition_xrefs":["ISBN:0721643949","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure mediated by a chemical signal","termid":"GO:0003044"},{"relation_name":"is_a","term_name":"endocrine process","termid":"GO:0050886"}],"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 systemic arterial blood pressure by hormone","synonyms":[{"name":"blood pressure regulation by hormone","type":"exact"},{"name":"hormonal control of blood pressure","type":"related"},{"name":"hormonal regulation of blood pressure","type":"exact"}],"termid":"GO:0001990"}


id: PBO:0065144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolactin receptor","termid":"PBO:0065144"}


id: GO:0042574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving retinal, a compound that plays an important role in the visual process in most vertebrates. In the retina, retinal combines with opsins to form visual pigments. Retinal is one of the forms of vitamin A.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinoid metabolic process","termid":"GO:0001523"},{"relation_name":"is_a","term_name":"aldehyde metabolic process","termid":"GO:0006081"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"retinal metabolic process","synonyms":[{"name":"retinal metabolism","type":"exact"},{"name":"retinaldehyde metabolic process","type":"exact"},{"name":"retinaldehyde metabolism","type":"exact"}],"termid":"GO:0042574"}


id: SO:0000591
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A tertiary structure in RNA where nucleotides in a loop form base pairs with a region of RNA downstream of the loop.","definition_xrefs":["RSC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_secondary_structure","termid":"SO:0000002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudoknot","secondary_identifiers":["http://en.wikipedia.org/wiki/Pseudoknot"],"termid":"SO:0000591"}


id: PBO:0051894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit alpha 3","termid":"PBO:0051894"}


id: GO:0120256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of an olefinic compound, any compound which contains a carbon-carbon double bond (aka C=C).","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"}],"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":"olefinic compound catabolic process","synonyms":[{"name":"alkene substituted compound breakdown","type":"exact"},{"name":"alkene substituted compound catabolic process","type":"exact"},{"name":"alkene substituted compound catabolism","type":"exact"},{"name":"alkene substituted compound degradation","type":"exact"}],"termid":"GO:0120256"}


id: PATO:0000265
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000265 relative visual_ability (obsolete PATO:0000265)","termid":"PATO:0000265"}


id: GO:0061712
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: N(6)-L-threonylcarbamoyladenine(37) in tRNA + sulfur-(sulfur carrier) + 2 S-adenosyl-L-methionine = 2-methylthio-N(6)-L-threonylcarbamoyladenine(37) in tRNA + S-adenosyl-L-homocysteine + (sulfur carrier) + L-methionine + 5'-deoxyadenosine.","definition_xrefs":["GOC:rynl"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA (N(6)-L-threonylcarbamoyladenosine(37)-C(2))-methylthiotransferase (obsolete GO:0061712)","termid":"GO:0061712"}


id: PR:O60117
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC16G5.03 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60117"],"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 RING finger protein C16G5.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16G5.03","synonyms":[{"name":"Spom972h-SPBC16G5.03","type":"exact"}],"termid":"PR:O60117"}


id: PBO:0116290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Highly variable glycoprotein localized to cell wall via GPI anchor; serine/threonine rich and highly similar to HPF1 haze-protective mannoprotein; necessary and sufficient for haze-positive phenotype in brewing strains which correlates with an expansion in the N-terminal serine-rich region; transcript is induced in both high and low pH environments","termid":"PBO:0116290"}


id: PBO:0069561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 833, pseudogene","termid":"PBO:0069561"}


id: GO:0032938
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of translation as a result of oxidative stress, a state often resulting from exposure to high levels of reactive oxygen species, e.g. superoxide anions, hydrogen peroxide (H2O2), and hydroxyl radicals.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of translational initiation in response to stress","termid":"GO:0032057"},{"relation_name":"is_a","term_name":"regulation of translation in response to oxidative stress","termid":"GO:0043556"},{"relation_name":"is_a","term_name":"regulation of translational initiation in response to stress","termid":"GO:0043558"}],"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:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of translation in response to oxidative stress","termid":"GO:0032938"}


id: PBO:0074657
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 47","termid":"PBO:0074657"}


id: PBO:0086165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for sorting proteins to the vacuole; Mvp1p and Vps1p act in concert to promote membrane traffic to the vacuole; participates in transcription initiation and/or early elongation of specific genes; interacts with 'foot domain' of RNA polymerase II; deletion results in abnormal CTD-Ser5 phosphorylation of RNA polymerase II at specific promoter regions; protein abundance increases in response to DNA replication stress","termid":"PBO:0086165"}


id: PBO:0065719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Prader Willi/Angelman region RNA 5","termid":"PBO:0065719"}


id: GO:1903518
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of single strand break repair.","definition_xrefs":["GOC:rl","GOC:TermGenie","GO_REF:0000058","PMID:17395247","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA repair","termid":"GO:0045739"},{"relation_name":"is_a","term_name":"regulation of single strand break repair","termid":"GO:1903516"},{"relation_name":"positively_regulates","term_name":"single strand break repair","termid":"GO:0000012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006281"},{"rel_name":"positively_regulates","termid":"GO:0006281"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006281","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"positive regulation of single strand break repair","synonyms":[{"name":"activation of single strand break repair","type":"narrow"},{"name":"up regulation of single strand break repair","type":"exact"},{"name":"up-regulation of single strand break repair","type":"exact"},{"name":"upregulation of single strand break repair","type":"exact"}],"termid":"GO:1903518"}


id: MONDO:0014776
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type III","termid":"MONDO:0019793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005559","MONDO:0000426"],"is_obsolete":false,"name":"spinocerebellar ataxia type 42","secondary_identifiers":["OMIM:616795","Orphanet:458803","NCIT:C171269","MEDGEN:902592","UMLS:C4225205","DOID:0111742","EFO:0009059","GARD:17811"],"synonyms":[{"name":"SCA42","type":"exact"},{"name":"spinocerebellar ataxia 42","type":"exact"},{"name":"spinocerebellar ataxia type 42","type":"exact"}],"termid":"MONDO:0014776","xrefs":{"Monarch":{"xref_id":"0014776"}}}


id: PBO:0050868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin degrading enzyme","termid":"PBO:0050868"}


id: MONDO:0001814
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete patent ductus arteriosus (obsolete MONDO:0001814)","termid":"MONDO:0001814","xrefs":{"Monarch":{"xref_id":"0001814"}}}


id: FYPO:0005366
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, does not occur during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein phosphorylation during vegetative growth","termid":"FYPO:0002033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0002494","FYPO:0001985","FYPO:0005447","FYPO:0002274"],"is_obsolete":false,"name":"abolished protein phosphorylation during mitosis","synonyms":[{"name":"abolished protein phosphorylation during M phase of mitotic cell cycle","type":"related"},{"name":"abolished protein phosphorylation during mitosis during vegetative growth","type":"exact"},{"name":"abolished protein phosphorylation during mitotic M phase","type":"related"},{"name":"protein phosphorylation abolished during mitosis","type":"exact"}],"termid":"FYPO:0005366"}


id: MONDO:1012484
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hoof wall separation syndrome, non-human animal","termid":"MONDO:1011772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hoof wall separation syndrome, horse","secondary_identifiers":["OMIA:001897-9796"],"termid":"MONDO:1012484","xrefs":{"Monarch":{"xref_id":"1012484"}}}


id: PBO:0047646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 3","termid":"PBO:0047646"}


id: MONDO:0018403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete female infertility due to an implantation defect (obsolete MONDO:0018403)","secondary_identifiers":["Orphanet:399882","ICD10CM:N97.2"],"synonyms":[{"name":"rare female infertility due to an implantation defect","type":"related"}],"termid":"MONDO:0018403","xrefs":{"Monarch":{"xref_id":"0018403"}}}


id: GO:0010022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a meristem becomes determinate (i.e. ceases to produce lateral organs and may or may not terminally differentiate).","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"meristem maintenance","termid":"GO:0010073"}],"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":"meristem determinacy","termid":"GO:0010022"}


id: PBO:0085099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear pore protein; involved in nuclear export of pre-tRNA and in re-export of mature tRNAs after their retrograde import from the cytoplasm; deletion mutation extends replicative lifespan, as does exclusion of Los1p from the nucleus in response to caloric restriction","termid":"PBO:0085099"}


id: MONDO:0004723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the liver. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C5753"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign endocrine neoplasm","termid":"MONDO:0000627"},{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"liver and intrahepatic bile duct neoplasm","termid":"MONDO:0024477"},{"relation_name":"is_a","term_name":"hepatobiliary benign neoplasm","termid":"MONDO:0859689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"liver leiomyoma","secondary_identifiers":["DOID:917","MEDGEN:232276","UMLS:C1333968"],"synonyms":[{"name":"hepatic leiomyoma","type":"exact"},{"name":"leiomyoma of liver","type":"exact"},{"name":"leiomyoma of the liver","type":"exact"},{"name":"liver leiomyoma","type":"exact"}],"termid":"MONDO:0004723","xrefs":{"Monarch":{"xref_id":"0004723"}}}


id: MONDO:0010968
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital glaucoma","termid":"MONDO:0020366"}],"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 3, primary infantile, B","secondary_identifiers":["GARD:2490","MESH:C536824","OMIM:600975","MEDGEN:331409","UMLS:C1832977"],"synonyms":[{"name":"GLC3 type B","type":"related"},{"name":"GLC3B","type":"exact"},{"name":"Glc3, type B","type":"related"},{"name":"glaucoma 3 primary infantile B","type":"related"},{"name":"glaucoma 3, primary infantile, B","type":"exact"},{"name":"glaucoma primary congenita type 3B","type":"related"},{"name":"glaucoma, primary congenital, type B","type":"related"},{"name":"primary congenital glaucoma","type":"related"},{"name":"primary congenital glaucoma type 3B","type":"related"}],"termid":"MONDO:0010968","xrefs":{"Monarch":{"xref_id":"0010968"}}}


id: PBO:0059779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 5","termid":"PBO:0059779"}


id: SO:0002312
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An element that always exists within the promoter region of a prokaryotic gene.","definition_xrefs":["GREEKC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"core_promoter_element","termid":"SO:0002309"},{"relation_name":"part_of","term_name":"prokaryotic_promoter","termid":"SO:0002222"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"core_prokaryotic_promoter_element","synonyms":[{"name":"core prokaryotic promoter element","type":"exact"},{"name":"general transcription factor binding site","type":"related"}],"termid":"SO:0002312"}


id: GO:0141112
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of bringing together chromosomes fragments resulting from DNA damage. Broken chromosome tethering during mitosis ensures clustered segregation of the fragments to a single daughter cell nucleus, facilitating re-ligation with limited chromosome scattering and loss and enhancing genome integrity.","definition_xrefs":["PMID:37316668","PMID:37165191"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome organization","termid":"GO:0051276"},{"relation_name":"part_of","term_name":"DNA damage response","termid":"GO:0006974"}],"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":"broken chromosome clustering","termid":"GO:0141112"}


id: MONDO:0003486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma characterized by the presence of cells with hyperchromatic nuclei, scant amount of cytoplasm, and peripheral nuclear palisading.","definition_xrefs":["NCIT:C54244"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"basaloid carcinoma","termid":"MONDO:0006102"}],"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":"basaloid squamous cell carcinoma","secondary_identifiers":["DOID:5522","icd11.foundation:1738201981","ICDO:8083/3","MEDGEN:266085","EFO:1001940","UMLS:C1266005"],"synonyms":[{"name":"basaloid carcinoma","type":"broad"},{"name":"basaloid carcinoma (morphologic abnormality)","type":"broad"},{"name":"basaloid squamous cell carcinoma","type":"exact"},{"name":"basaloid squamous cell carcinoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003486","xrefs":{"Monarch":{"xref_id":"0003486"}}}


id: PBO:0083142
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; almost completely overlaps 3' end of verified gene NUP53/YMR153W","termid":"PBO:0083142"}


id: PBO:0073647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"salt inducible kinase 1","termid":"PBO:0073647"}


id: GO:0004994
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with somatostatin to initiate a change in cell activity. Somatostatin is a peptide hormone that regulates the endocrine system by signaling via G protein-coupled somatostatin receptors. Somatostatin has two active forms produced by proteolytic cleavage: a 14 amino acid peptide (SST-14) and a 28 amino acid peptide (SST-28).","definition_xrefs":["Wikipedia:Somatostatin","GOC:ai","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide receptor activity","termid":"GO:0008188"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"somatostatin receptor activity","synonyms":[{"name":"GHIH receptor activity","type":"exact"},{"name":"SRIF receptor activity","type":"exact"},{"name":"SST receptor activity","type":"exact"},{"name":"growth hormone-inhibiting hormone receptor activity","type":"exact"},{"name":"somatotrophin release inhibiting factor receptor activity","type":"exact"}],"termid":"GO:0004994"}


id: PBO:0040323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase F1 subunit epsilon pseudogene 2","termid":"PBO:0040323"}


id: MONDO:0007025
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The primary sore of syphilis, a painless indurated, eroded papule, occurring at the site of entry of the infection.","definition_xrefs":["EFO:1001247"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syphilis","termid":"MONDO:0005976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chancre","secondary_identifiers":["MEDGEN:671172","MESH:D002601","UMLS:C0600049"],"termid":"MONDO:0007025","xrefs":{"Monarch":{"xref_id":"0007025"}}}


id: GO:0014844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of myoblasts, resulting in the expansion of the cell population. This occurs as part of skeletal muscle regeneration. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["CL:0000056","GOC:mtg_muscle","GOC:ef","PMID:16607119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myoblast proliferation","termid":"GO:0051450"},{"relation_name":"part_of","term_name":"skeletal muscle tissue regeneration","termid":"GO:0043403"}],"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":"myoblast proliferation involved in skeletal muscle regeneration","termid":"GO:0014844"}


id: PBO:0109639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid early transcript 1F (pseudogene)","termid":"PBO:0109639"}


id: PBO:0039642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adaptor related protein complex 1 associated regulatory protein","termid":"PBO:0039642"}


id: MONDO:0012658
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Brachydactyly type B2 is a rare, genetic congenital limb malformation disorder characterized by hypoplasia/aplasia of distal and/or middle phalanges in fingers and toes II-V (frequently severe in fingers/toes IV-V, milder in fingers/toes II-III) in association with proximal, and occasionally distal, symphalangism, fusion of carpal/tarsal bones and partial cutaneous syndactyly. Additional reported features include proximal placement of thumbs, sensorineural hearing loss and farsightedness.","definition_xrefs":["Orphanet:140908"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome with brachydactyly (obsolete MONDO:0019066)","termid":"MONDO:0019066"},{"relation_name":"is_a","term_name":"brachydactyly type B","termid":"MONDO:0019676"},{"relation_name":"is_a","term_name":"NOG-related symphalangism spectrum disorder","termid":"MONDO:0100521"}],"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":"brachydactyly type B2","secondary_identifiers":["GARD:16963","DOID:0110975","UMLS:C1969652","icd11.foundation:891810441","SCTID:770406002","MEDGEN:409880","OMIM:611377"],"synonyms":[{"name":"BDB2","type":"exact"},{"name":"brachydactyly, type B2","type":"related"}],"termid":"MONDO:0012658","xrefs":{"Monarch":{"xref_id":"0012658"}}}


id: FYPO:0007669
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 a cell is viable, has a larger volume than normal, and undergoes one or more rounds of rereplication of the entire genome. 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":["PMID:8121488","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal negative regulation of mitotic DNA replication initiation","termid":"FYPO:0000216"},{"relation_name":"is_a","term_name":"viable swollen vegetative cell","termid":"FYPO:0002377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000631","FYPO:0000004","FYPO:0001320"],"is_obsolete":false,"name":"viable swollen vegetative cell with complete DNA rereplication","synonyms":[{"name":"viable enlarged vegetative cell with complete DNA rereplication","type":"related"},{"name":"viable large vegetative cell with complete DNA rereplication","type":"related"},{"name":"viable swollen cell with complete DNA rereplication during vegetative growth","type":"exact"},{"name":"viable swollen vegetative cell with abnormal negative regulation of mitotic DNA replication initiation resulting in complete rereplication","type":"exact"},{"name":"viable swollen vegetative cell with complete DNA rereplication during mitotic cell cycle","type":"related"},{"name":"viable swollen vegetative cell with increased ploidy","type":"exact"},{"name":"viable vegetative cell with increased cell size and complete DNA rereplication","type":"related"},{"name":"viable vegetative cell with increased cell volume and complete DNA rereplication","type":"exact"}],"termid":"FYPO:0007669"}


id: PBO:0117234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyamine transmembrane transporter family","termid":"PBO:0117234"}


id: GO:0120501
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-methionyl-[F-actin] + NADPH + O2 + H+ = L-methionyl-(R)-S-oxide-[F-actin] + NADP+ + H2O.","definition_xrefs":["RHEA:51308"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"F-actin monooxygenase activity","secondary_identifiers":["EC:1.14.13.225"],"termid":"GO:0120501"}


id: PBO:0079311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 5","termid":"PBO:0079311"}


id: GO:0036434
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ethylnitronate + FMNH(2) + O2 = acetaldehyde + FMN + H2O + H+ + nitrite.","definition_xrefs":["RHEA:26458"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of one atom of oxygen (internal monooxygenases or internal mixed function oxidases)","termid":"GO:0016703"}],"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:0003674","GO:0016491"],"is_obsolete":false,"name":"nitronate monooxygenase (FMN-linked) activity","secondary_identifiers":["KEGG_REACTION:R00025"],"termid":"GO:0036434"}


id: PBO:0070098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 12 pseudogene","termid":"PBO:0070098"}


id: MONDO:0020617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete blood group--ok (obsolete MONDO:0020617)","secondary_identifiers":["OMIM:111380"],"synonyms":[{"name":"BLOOD GROUP--OK","type":"related"},{"name":"OK","type":"related"},{"name":"blood group, OK","type":"exact"}],"termid":"MONDO:0020617","xrefs":{"Monarch":{"xref_id":"0020617"}}}


id: GO:0030111
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the activity of the Wnt signal transduction pathway.","definition_xrefs":["GOC:dph","GOC:tb","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"Wnt signaling pathway","termid":"GO:0016055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of Wnt signaling pathway","secondary_identifiers":["Reactome:R-HSA-8939256","GO:0008590"],"synonyms":[{"name":"regulation of Wnt receptor signaling pathway","type":"exact"},{"name":"regulation of Wnt receptor signalling pathway","type":"exact"},{"name":"regulation of Wnt-activated signaling pathway","type":"exact"},{"name":"regulation of frizzled signaling pathway","type":"exact"},{"name":"regulation of frizzled signalling pathway","type":"exact"}],"termid":"GO:0030111"}


id: PBO:0081276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 43","termid":"PBO:0081276"}


id: GO:0062092
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cytosolic complex that functions as an substrate-specific adaptor, linking the cytosolic iron-sulfur protein assembly (CIA) targeting complex to apo-Rli1p, an ABC protein involved in ribosome recycling, facilitating Fe-S cluster insertion and the maturation of the Rli1p.","definition_xrefs":["PMID:26182403"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005829"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005829","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"Yae1-Lto1 complex","termid":"GO:0062092"}


id: PBO:0083510
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 ORF CUP2/YGL166W","termid":"PBO:0083510"}


id: PBO:0075216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sentan, cilia apical structure protein","termid":"PBO:0075216"}


id: PBO:0052193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KCNMB2 antisense RNA 1","termid":"PBO:0052193"}


id: MONDO:0017909
data:
  {"annotated_genes":["SJAG_01351"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87597],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009947"},{"annotations":[88026],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009284"}]},"cv_name":"mondo","definition":"Glutathione synthetase deficiency is characterized by hemolytic anemia, associated with metabolic acidosis and 5-oxoprolinuria in moderate forms, and with progressive neurological symptoms and recurrent bacterial infections in the most severe forms.","definition_xrefs":["Orphanet:32"],"direct_ancestors":[{"relation_name":"is_a","term_name":"defective phagocytic cell engulfment","termid":"MONDO:0024626"},{"relation_name":"is_a","term_name":"inherited glutathione metabolism disease","termid":"MONDO:0040566"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01351":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019241"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005046","MONDO:0019241"],"is_obsolete":false,"name":"inherited glutathione synthetase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C536835","NCIT:C128193","SCTID:234589002","GARD:10047","DOID:0080699"],"synonyms":[{"name":"5-oxoprolinuria","type":"exact"},{"name":"GSSD","type":"exact"},{"name":"glutathione synthetase deficiency","type":"exact"},{"name":"inborn error of glutathione synthase activity","type":"exact"},{"name":"inborn glutathione synthase activity disorder","type":"exact"},{"name":"inherited glutathione synthetase deficiency","type":"exact"},{"name":"oxoprolinase deficiency","type":"related"},{"name":"pyroglutamic aciduria","type":"exact"},{"name":"pyroglutamicaciduria","type":"exact"},{"name":"rare inborn error of glutathione synthase activity","type":"exact"}],"termid":"MONDO:0017909","terms_by_termid":{"MONDO:0009284":null,"MONDO:0009947":null},"xrefs":{"Monarch":{"xref_id":"0017909"}}}


id: PBO:0001609
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.107","termid":"PBO:0001609"}


id: FYPO:0005744
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which protein transport is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization","termid":"FYPO:0001370"},{"relation_name":"is_a","term_name":"abnormal transport","termid":"FYPO:0001720"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein transport","termid":"FYPO:0005744"}


id: GO:0030133
data:
  {"annotated_genes":["SJAG_02282","SJAG_03153","SJAG_04509","SJAG_00669","SJAG_01189","SJAG_00379","SJAG_04517","SJAG_01633","SJAG_03915","SJAG_02349","SJAG_00916","SJAG_01309","SJAG_03558","SJAG_02539","SJAG_04565","SJAG_05345","SJAG_00072","SJAG_00557","SJAG_01939","SJAG_05344","SJAG_00284","SJAG_02240","SJAG_00906","SJAG_04609","SJAG_01809","SJAG_04023","SJAG_04513","SJAG_03907"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[76430,121308],"is_not":false,"summary":null,"term":"GO:0030133"},{"annotations":[62727,79399,114752,114964],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030121"},{"annotations":[58962,66569],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030130"},{"annotations":[97372,77404,76956,78870,76598,78294,73086,73208,74761,80242],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030127"},{"annotations":[102969,75649,68748,77879,72185],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0012507"},{"annotations":[89692,117448],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070382"},{"annotations":[73673,79078],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034044"},{"annotations":[102077],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030140"}]},"cv_name":"cellular_component","definition":"Any of the vesicles of the constitutive secretory pathway, which carry cargo from the endoplasmic reticulum to the Golgi, between Golgi cisternae, from the Golgi to the ER (retrograde transport) or to destinations within or outside the cell.","definition_xrefs":["GOC:mah","PMID:22160157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle","termid":"GO:0031410"},{"relation_name":"part_of","term_name":"endomembrane system","termid":"GO:0012505"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00072":null,"SJAG_00284":null,"SJAG_00379":null,"SJAG_00557":null,"SJAG_00669":null,"SJAG_00906":null,"SJAG_00916":null,"SJAG_01189":null,"SJAG_01309":null,"SJAG_01633":null,"SJAG_01809":null,"SJAG_01939":null,"SJAG_02240":null,"SJAG_02282":null,"SJAG_02349":null,"SJAG_02539":null,"SJAG_03153":null,"SJAG_03558":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_04023":null,"SJAG_04509":null,"SJAG_04513":null,"SJAG_04517":null,"SJAG_04565":null,"SJAG_04609":null,"SJAG_05344":null,"SJAG_05345":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0031410","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"transport vesicle","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"PMID:30726171":null},"secondary_identifiers":["NIF_Subcellular:sao885490876"],"synonyms":[{"name":"Golgi to vacuole transport vesicle","type":"narrow"},{"name":"Golgi-vacuole transport vesicle","type":"narrow"},{"name":"constitutive secretory pathway transport vesicle","type":"exact"},{"name":"secretory vesicle","type":"related"}],"termid":"GO:0030133","terms_by_termid":{"GO:0012507":null,"GO:0030121":null,"GO:0030127":null,"GO:0030130":null,"GO:0030133":null,"GO:0030140":null,"GO:0034044":null,"GO:0070382":null}}


id: MONDO:0004548
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare sex cord-stromal tumor that arises from the testis in adults. Gynecomastia is present in approximately a quarter of the patients. Several morphologic patterns have been identified and include insular, gyriform, trabecular, pseudosarcomatous, and solid. Metastases occur in approximately twenty percent of the cases.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"testicular granulosa cell tumor","termid":"MONDO:0003395"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adult type testicular granulosa cell tumor","secondary_identifiers":["DOID:8394","MEDGEN:272840","NCIT:C39946","UMLS:C1515284"],"synonyms":[{"name":"adult testicular granulosa cell tumor","type":"exact"},{"name":"adult testicular granulosa cell tumour","type":"exact"},{"name":"adult type testicular granulosa cell tumor","type":"exact"}],"termid":"MONDO:0004548","xrefs":{"Monarch":{"xref_id":"0004548"}}}


id: PBO:0055164
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 2584","termid":"PBO:0055164"}


id: GO:0003731
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Interacting selectively with the 7-methylguanosine cap at the 5' end of a nascent messenger RNA transcript.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete mRNA cap binding (obsolete GO:0003731)","synonyms":[{"name":"mRNA cap binding","type":"exact"}],"termid":"GO:0003731"}


id: PBO:0056901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIER family member 3","termid":"PBO:0056901"}


id: PBO:0029774
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_spore_population_with_abnormal_spore_shape_(obsolete_FYPO:0002465)","termid":"PBO:0029774"}


id: GO:0071834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of a mating pheromone, a peptide hormone that induces a behavioral or physiological response(s) from a responding organism or cell, that contributes to a process of sexual reproduction.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide hormone secretion","termid":"GO:0030072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0023052","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"mating pheromone secretion","synonyms":[{"name":"mating-type pheromone secretion","type":"exact"}],"termid":"GO:0071834"}


id: GO:0035386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the Roundabout signaling pathway.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"Roundabout signaling pathway","termid":"GO:0035385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of Roundabout signaling pathway","synonyms":[{"name":"regulation of Roundabout signalling pathway","type":"exact"}],"termid":"GO:0035386"}


id: GO:0014836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a satellite cell becomes restricted such that it will develop into a myoblast. This occurs as part of skeletal muscle regeneration. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["PMID:16607119","GOC:mtg_muscle","CL:0000056","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myoblast fate commitment","termid":"GO:0048625"},{"relation_name":"part_of","term_name":"myoblast differentiation involved in skeletal muscle regeneration","termid":"GO:0014835"}],"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":"myoblast fate commitment involved in skeletal muscle regeneration","termid":"GO:0014836"}


id: MONDO:0018837
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Vasculitis, characterized by inflammatory lesions in the wall of vessels, may be due to different viruses.","definition_xrefs":["Orphanet:48435"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary vasculitis","termid":"MONDO:0018640"},{"relation_name":"is_a","term_name":"post-infectious disorder","termid":"MONDO:0021669"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postinfectious vasculitis","secondary_identifiers":["GARD:18835","UMLS:C4510302","SCTID:724063005","MEDGEN:1376009"],"termid":"MONDO:0018837","xrefs":{"Monarch":{"xref_id":"0018837"}}}


id: GO:0060380
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of binding to single-stranded telomeric DNA.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of single-stranded telomeric DNA binding (obsolete GO:0060380)","synonyms":[{"name":"regulation of telomeric ssDNA binding","type":"exact"}],"termid":"GO:0060380"}


id: GO:0002128
data:
  {"annotated_genes":["SJAG_01269","SJAG_02352","SJAG_04649"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116802],"is_not":false,"summary":null,"term":"GO:0002128"},{"annotations":[99724,104792],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002130"}]},"cv_name":"biological_process","definition":"The process that results in the modification of the sugar of a nucleoside in tRNA at the 2'O position.","definition_xrefs":["ISBN:155581073X","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA methylation","termid":"GO:0030488"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01269":null,"SJAG_02352":null,"SJAG_04649":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0006399","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"tRNA nucleoside ribose methylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0002128","terms_by_termid":{"GO:0002128":null,"GO:0002130":null}}


id: MONDO:0011529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia.","definition_xrefs":["Orphanet:98768"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type I","termid":"MONDO:0019792"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"spinocerebellar ataxia type 13","secondary_identifiers":["DOID:0050963","MEDGEN:344297","icd11.foundation:1191033828","MESH:C537195","SCTID:719209002","GARD:9611","OMIM:605259","UMLS:C1854488"],"synonyms":[{"name":"SCA13","type":"exact"},{"name":"autosomal dominant cerebellar ataxia with intellectual disability","type":"related"},{"name":"autosomal dominant cerebellar ataxia with mental retardation","type":"related"},{"name":"cerebellar ataxia, autosomal dominant with intellectual disability","type":"related"},{"name":"cerebellar ataxia, autosomal dominant with mental retardation","type":"related"},{"name":"spinocerebellar ataxia 13","type":"related"},{"name":"spinocerebellar ataxia type 13","type":"exact"}],"termid":"MONDO:0011529","xrefs":{"Monarch":{"xref_id":"0011529"}}}


id: FYPO:0001691
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing paraquat.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0000257","FYPO:0002060","FYPO:0002058","FYPO:0000003","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on paraquat","synonyms":[{"name":"normal cell population growth in presence of paraquat","type":"exact"},{"name":"normal cell population growth on paraquat","type":"exact"},{"name":"normal cellular response to paraquat","type":"related"},{"name":"normal vegetative cell population growth on paraquat","type":"exact"}],"termid":"FYPO:0001691"}


id: GO:0106363
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-cysteinyl-[protein] + S-adenosyl-L-methionine = H+ + S-adenosyl-L-homocysteine + S-methyl-L-cysteinyl-[protein].","definition_xrefs":["PMID:21481189","PMID:25412445","RHEA:66544","PMID:24235145","GOC:sp","PMID:22158122"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-methyltransferase activity","termid":"GO:0008172"},{"relation_name":"is_a","term_name":"protein methyltransferase activity","termid":"GO:0008276"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0008276","GO:0140096","GO:0016741","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"protein-cysteine methyltransferase activity","synonyms":[{"name":"protein cysteine methylase activity","type":"exact"},{"name":"protein cysteine methyltransferase activity","type":"exact"}],"termid":"GO:0106363"}


id: PBO:0002398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial serine-tRNA ligase (predicted)","termid":"PBO:0002398"}


id: GO:1905057
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Any voltage-gated calcium channel activity that is involved in regulation of postsynaptic cytosolic calcium ion concentration.","definition_xrefs":["PMID:20734177","GOC:TermGenie","GO_REF:0000061"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated calcium channel activity involved in regulation of cytosolic calcium levels","termid":"GO:0099511"}],"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:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"voltage-gated calcium channel activity involved in regulation of postsynaptic cytosolic calcium levels","synonyms":[{"name":"depolarization-activated voltage gated calcium channel activity involved in regulation of postsynaptic cytosolic calcium ion concentration","type":"exact"},{"name":"depolarization-activated voltage-gated calcium channel activity involved in regulation of postsynaptic cytosolic calcium ion concentration","type":"exact"},{"name":"depolarization-activated voltage-gated calcium channel involved in regulation of postsynaptic cytosolic calcium ion concentration","type":"exact"},{"name":"dihydropyridine-sensitive calcium channel activity involved in regulation of postsynaptic cytosolic calcium ion concentration","type":"narrow"},{"name":"voltage gated calcium channel activity involved in regulation of postsynaptic cytosolic calcium ion concentration","type":"exact"},{"name":"voltage-dependent calcium channel activity involved in regulation of postsynaptic cytosolic calcium ion concentration","type":"exact"},{"name":"voltage-gated calcium channel activity involved in regulation of postsynaptic cytosolic calcium levels","type":"exact"},{"name":"voltage-gated calcium ion channel activity involved in regulation of postsynaptic cytosolic calcium ion concentration","type":"exact"},{"name":"voltage-sensitive calcium channel involved in regulation of postsynaptic cytosolic calcium ion concentration","type":"exact"}],"termid":"GO:1905057"}


id: PBO:0039817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor GTPase activating protein 1","termid":"PBO:0039817"}


id: PBO:0071017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 19","termid":"PBO:0071017"}


id: PBO:0113100
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dihydrouridine synthase; modifies pre-tRNAs at U20a and U20b of the D loop; member of a widespread family of conserved proteins including Smm1p, Dus1p, and Dus3p","termid":"PBO:0113100"}


id: GO:0060337
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by type I interferon binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription. Type I interferons include the interferon-alpha, beta, delta, episilon, zeta, kappa, tau, and omega gene families.","definition_xrefs":["GOC:add","GOC:dph","GOC:signaling","PMID:32464097"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interferon-mediated signaling pathway","termid":"GO:0140888"},{"relation_name":"part_of","term_name":"cellular response to type I interferon","termid":"GO:0071357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"type I interferon-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-909733"],"synonyms":[{"name":"type I interferon signaling pathway","type":"exact"},{"name":"type I interferon-activated signaling pathway","type":"exact"}],"termid":"GO:0060337"}


id: GO:0031380
data:
  {"annotated_genes":["SJAG_02725","SJAG_03193","SJAG_03356"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[71868,73670,119972],"is_not":false,"summary":null,"term":"GO:0031380"}]},"cv_name":"cellular_component","definition":"A complex required for RNAi mediated heterochromatin assembly. In S. pombe this contains RNA-directed RNA polymerase, a putative helicase and a protein containing a pap25 associated domain.","definition_xrefs":["PMID:15607976","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA-directed RNA polymerase complex","termid":"GO:0031379"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02725":null,"SJAG_03193":null,"SJAG_03356":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:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"nuclear RNA-directed RNA polymerase complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"RDRC","type":"exact"},{"name":"Rdr1 complex","type":"narrow"}],"termid":"GO:0031380","terms_by_termid":{"GO:0031380":null}}


id: FYPO:0002930
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which polyadenylated RNA molecules have poly(A) tails of that are shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal poly(A) tail length","termid":"FYPO:0002929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002929"}],"interesting_parent_ids":["FYPO:0002929","FYPO:0001985"],"is_obsolete":false,"name":"decreased poly(A) tail length","synonyms":[{"name":"decreased polyA sequence length","type":"exact"},{"name":"decreased polyA tail length","type":"exact"},{"name":"reduced poly(A) tail length","type":"exact"},{"name":"short poly(a) tails","type":"exact"}],"termid":"FYPO:0002930"}


id: GO:0003365
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification and formation of anisotropic intracellular organization that contributes to the self-propelled directed movement of an ameboid cell.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of cell polarity","termid":"GO:0030010"},{"relation_name":"part_of","term_name":"ameboidal-type cell migration","termid":"GO:0001667"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0008150","GO:0007163"],"is_obsolete":false,"name":"establishment of cell polarity involved in ameboidal cell migration","termid":"GO:0003365"}


id: GO:0072439
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about whether DNA replication is complete is received and converted into a molecular signal, contributing to a meiotic DNA replication checkpoint.","definition_xrefs":["GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in meiotic DNA replication checkpoint (obsolete GO:0072439)","synonyms":[{"name":"meiotic DNA replication checkpoint sensor mechanism","type":"related"},{"name":"meiotic DNA replication checkpoint sensor process","type":"related"},{"name":"sensing involved in meiotic DNA replication checkpoint","type":"related"}],"termid":"GO:0072439"}


id: MONDO:0100527
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare primary bone dysplasia with increased bone density characterized by lethal neonatal dwarfism with hydrops, narrow chest and short limbs with extensive cortical thickening of all long bones, ribs, clavicles and scapulae, and coronal clefts in vertebral bodies.","definition_xrefs":["Orphanet:2204"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysplastic cortical hyperostosis","termid":"MONDO:0016357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"dysplastic cortical hyperostosis, Kozlowski-Tsuruta type","secondary_identifiers":["GARD:2022","MEDGEN:1830504","UMLS:C5780027"],"synonyms":[{"name":"Kozlowski-Tsuruta syndrome","type":"exact"}],"termid":"MONDO:0100527","xrefs":{"Monarch":{"xref_id":"0100527"}}}


id: GO:0009154
data:
  {"annotated_genes":["SJAG_00461","SJAG_02135","SJAG_02369","SJAG_02945","SJAG_02785","SJAG_05314","SJAG_00605","SJAG_00027","SJAG_02107","SJAG_06622","SJAG_02796","SJAG_01310","SJAG_04334","SJAG_04048","SJAG_03828","SJAG_04495","SJAG_00685","SJAG_02009","SJAG_03903","SJAG_04870","SJAG_02481","SJAG_04192","SJAG_06621","SJAG_03660","SJAG_00839","SJAG_03373"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81054],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901911"},{"annotations":[118362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006198"},{"annotations":[107376,118333,111346,99868,111344,105284,107375,107745,107374,96380,105543,111343,79614,111341,100139,111342,111345,107746,111340,74188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"},{"annotations":[90422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061613"},{"annotations":[74840,77909],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045820"},{"annotations":[71751],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006110"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a purine ribonucleotide, a compound consisting of ribonucleoside (a purine base linked to a ribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide catabolic process","termid":"GO:0006195"},{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"ribonucleotide catabolic process","termid":"GO:0009261"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00461":null,"SJAG_00605":null,"SJAG_00685":null,"SJAG_00839":null,"SJAG_01310":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02369":null,"SJAG_02481":null,"SJAG_02785":null,"SJAG_02796":null,"SJAG_02945":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_04048":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_04870":null,"SJAG_05314":null,"SJAG_06621":null,"SJAG_06622":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":"purine ribonucleotide catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"purine ribonucleotide breakdown","type":"exact"},{"name":"purine ribonucleotide catabolism","type":"exact"},{"name":"purine ribonucleotide degradation","type":"exact"}],"termid":"GO:0009154","terms_by_termid":{"GO:0006110":null,"GO:0006198":null,"GO:0045820":null,"GO:0061613":null,"GO:0061621":null,"GO:1901911":null}}


id: PR:Q10446
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A glucose-induced degradation protein 8 homolog that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01905"],"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 C12B10.13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC12B10.13","secondary_identifiers":["UniProtKB:Q10446"],"synonyms":[{"name":"Spom972h-GID8","type":"exact"}],"termid":"PR:Q10446"}


id: GO:1901687
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glutathione derivative.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"},{"relation_name":"is_a","term_name":"glutathione derivative metabolic process","termid":"GO:1901685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006790"],"is_obsolete":false,"name":"glutathione derivative biosynthetic process","secondary_identifiers":["Reactome:R-HSA-156590"],"synonyms":[{"name":"glutathione derivative anabolism","type":"exact"},{"name":"glutathione derivative biosynthesis","type":"exact"},{"name":"glutathione derivative formation","type":"exact"},{"name":"glutathione derivative synthesis","type":"exact"}],"termid":"GO:1901687"}


id: MONDO:1011450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Xanthinuria that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"xanthinuria, non-human animal","secondary_identifiers":["OMIA:001283"],"termid":"MONDO:1011450","xrefs":{"Monarch":{"xref_id":"1011450"}}}


id: MONDO:0009396
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":"hyperparathyroidism, neonatal self-limited primary, with hypercalciuria","secondary_identifiers":["MEDGEN:344611","OMIM:239199","UMLS:C1855924","MESH:C565496"],"synonyms":[{"name":"hyperparathyroidism, neonatal self-limited primary, with hypercalciuria","type":"exact"}],"termid":"MONDO:0009396","xrefs":{"Monarch":{"xref_id":"0009396"}}}


id: PBO:0031690
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_oxidative_phosphorylation","termid":"PBO:0031690"}


id: PBO:0116973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADORA1 antisense RNA 1","termid":"PBO:0116973"}


id: MONDO:0030841
data:
  {"annotated_genes":["SJAG_02748"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87595],"is_not":false,"summary":null,"term":"MONDO:0030841"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mismatch repair cancer syndrome","termid":"MONDO:0031219"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02748":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0021190"],"is_obsolete":false,"name":"mismatch repair cancer syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619097","MEDGEN:1733656","UMLS:C5436807","GARD:18363"],"synonyms":[{"name":"MMRCS3","type":"exact"},{"name":"mismatch repair cancer syndrome 3","type":"exact"}],"termid":"MONDO:0030841","terms_by_termid":{"MONDO:0030841":null},"xrefs":{"Monarch":{"xref_id":"0030841"}}}


id: MONDO:0009576
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"corneal disorder","termid":"MONDO:0000942"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"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":"megalocornea","secondary_identifiers":["MEDGEN:1807965","MESH:C562829","DOID:0060305","SCTID:268158009","UMLS:C5574682","icd11.foundation:58849242","OMIM:249300","HP:0007660","HP:0000485"],"synonyms":[{"name":"anterior megalophthalmos","type":"exact"},{"name":"megalocornea","type":"exact"},{"name":"megalocornea (disease)","type":"exact"}],"termid":"MONDO:0009576","xrefs":{"Monarch":{"xref_id":"0009576"}}}


id: GO:0034485
data:
  {"annotated_genes":["SJAG_00063"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110245],"is_not":false,"summary":null,"term":"GO:0034485"}]},"cv_name":"molecular_function","definition":"1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol-3,4,5-trisphosphate) + H2O = 1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol-3,4-bisphosphate) + phosphate.","definition_xrefs":["EC:3.1.3.86","GOC:pf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol trisphosphate phosphatase activity","termid":"GO:0034594"},{"relation_name":"is_a","term_name":"phosphatidylinositol phosphate 5-phosphatase activity","termid":"GO:0034595"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00063":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:25528","MetaCyc:RXN-10036","Reactome:R-HSA-1675949"],"termid":"GO:0034485","terms_by_termid":{"GO:0034485":null}}


id: PBO:0053288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIMD1 antisense RNA 1","termid":"PBO:0053288"}


id: GO:0102805
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: codeine + 2-oxoglutarate + O2 = morphine + formaldehyde + succinate + CO2.","definition_xrefs":["RHEA:27413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"codeine O-demethylase activity","secondary_identifiers":["MetaCyc:RXN-8152","EC:1.14.11.32"],"termid":"GO:0102805"}


id: GO:1902132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (+)-lariciresinol.","definition_xrefs":["PMID:8910615","PMID:9872995","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan biosynthetic process","termid":"GO:0009807"},{"relation_name":"is_a","term_name":"primary alcohol biosynthetic process","termid":"GO:0034309"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"ether biosynthetic process","termid":"GO:1901503"},{"relation_name":"is_a","term_name":"(+)-lariciresinol metabolic process","termid":"GO:1902130"}],"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:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"(+)-lariciresinol biosynthetic process","synonyms":[{"name":"(+)-lariciresinol anabolism","type":"exact"},{"name":"(+)-lariciresinol biosynthesis","type":"exact"},{"name":"(+)-lariciresinol formation","type":"exact"},{"name":"(+)-lariciresinol synthesis","type":"exact"}],"termid":"GO:1902132"}


id: FYPO:0001762
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 tRNA modification, the covalent alteration of one or more nucleotides within a tRNA molecule, is normal (i.e. indistinguishable from wild type).","definition_xrefs":["GO:0006400","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA processing","termid":"FYPO:0001980"},{"relation_name":"is_a","term_name":"normal RNA metabolic process","termid":"FYPO:0004850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal tRNA modification","synonyms":[{"name":"normal tRNA modification during mitotic cell cycle","type":"related"},{"name":"normal tRNA modification during vegetative growth","type":"exact"}],"termid":"FYPO:0001762"}


id: MONDO:0016697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ependymoma","termid":"MONDO:0016698"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"low grade ependymoma","secondary_identifiers":["icd11.foundation:641455939","Orphanet:251633"],"termid":"MONDO:0016697","xrefs":{"Monarch":{"xref_id":"0016697"}}}


id: GO:0048692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of axon extension involved in regeneration.","definition_xrefs":["GOC:dgh","GOC:dph","GOC:jid","GOC:lm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of axon extension","termid":"GO:0030517"},{"relation_name":"is_a","term_name":"negative regulation of sprouting of injured axon","termid":"GO:0048688"},{"relation_name":"is_a","term_name":"regulation of axon extension involved in regeneration","termid":"GO:0048690"},{"relation_name":"negatively_regulates","term_name":"axon extension involved in regeneration","termid":"GO:0048677"}],"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 axon extension involved in regeneration","synonyms":[{"name":"down regulation of axon extension involved in regeneration","type":"exact"},{"name":"down-regulation of axon extension involved in regeneration","type":"exact"},{"name":"downregulation of axon extension involved in regeneration","type":"exact"},{"name":"inhibition of axon extension involved in regeneration","type":"narrow"}],"termid":"GO:0048692"}


id: GO:0005712
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A connection formed between chromatids, visible during meiosis, thought to be the point of the interchange involved in crossing-over.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"condensed nuclear chromosome","termid":"GO:0000794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005694","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"chiasma","secondary_identifiers":["Wikipedia:Chiasma_(genetics)"],"termid":"GO:0005712"}


id: PBO:0060117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 18","termid":"PBO:0060117"}


id: PR:O74345
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ucp3 gene.","definition_xrefs":["UniProtKB:O74345","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":"UBA domain-containing protein 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21D10.05c","synonyms":[{"name":"Spom972h-ucp3","type":"exact"}],"termid":"PR:O74345"}


id: PBO:0042535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDK5 regulatory subunit associated protein 2","termid":"PBO:0042535"}


id: FYPO:0001551
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 protein measured in a cell during a cellular response to zinc ion starvation is higher than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0006551","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased protein level during cellular response to zinc ion starvation","synonyms":[{"name":"increased protein accumulation during cellular response to zinc ion starvation","type":"related"},{"name":"increased protein level during cellular response to zinc ion depletion","type":"exact"},{"name":"increased protein level during cellular response to zinc ion deprivation","type":"exact"},{"name":"increased protein level during cellular response to zinc ion starvation during mitotic cell cycle","type":"related"},{"name":"increased protein level during cellular response to zinc ion starvation during vegetative growth","type":"exact"},{"name":"increased protein level during cellular response to zinc starvation","type":"exact"}],"termid":"FYPO:0001551"}


id: MONDO:0008297
data:
  {"annotated_genes":["SJAG_02876"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87551],"is_not":false,"summary":null,"term":"MONDO:0008297"},{"annotations":[88196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957577"}]},"cv_name":"mondo","definition":"Variegate porphyria is a form of acute hepatic porphyria characterized by the occurrence of neuro-visceral attacks with or without the presence of cutaneous lesions.","definition_xrefs":["Orphanet:79473"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hepatic porphyria","termid":"MONDO:0002520"},{"relation_name":"is_a","term_name":"inherited porphyria","termid":"MONDO:0019142"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02876":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019142"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005066","MONDO:0002515","MONDO:0019142","MONDO:0005093"],"is_obsolete":false,"name":"variegate porphyria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:1200814","GARD:7848","NCIT:C85219","SCTID:58275005","OMIM:176200","MESH:D046350","DOID:4346","MEDGEN:58118","NANDO:2201265","icd11.foundation:1227474618","UMLS:C0162532"],"synonyms":[{"name":"PPOX deficiency","type":"related"},{"name":"Protocoproporphyria","type":"exact"},{"name":"VP","type":"related"},{"name":"porphyria variegata","type":"related"},{"name":"porphyria variegata, susceptibility to","type":"related"},{"name":"porphyria variegate","type":"related"},{"name":"porphyria, South African type","type":"related"},{"name":"protoporphyrinogen oxidase deficiency","type":"exact"},{"name":"variegate porphyria","type":"exact"},{"name":"variegate porphyria, homozygous variant","type":"related"}],"termid":"MONDO:0008297","terms_by_termid":{"MONDO:0008297":null,"MONDO:0957577":null},"xrefs":{"Monarch":{"xref_id":"0008297"}}}


id: SO:0000549
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome generated by recombination between two inversions; has a duplication at one end and presumed to have a deficiency or duplication at the other end of the inversion.","definition_xrefs":["FB:km"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intrachromosomal_duplication","termid":"SO:1000038"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inversion_derived_duplication_plus_aneuploid","synonyms":[{"name":"inversion derived duplication plus aneuploid","type":"exact"}],"termid":"SO:0000549"}


id: PBO:0075734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRP14 pseudogene 2","termid":"PBO:0075734"}


id: MONDO:0010798
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome is characterized by onset of proximal tubulopathy in the first year of life, followed by progressive development during childhood of skin anomalies (erythrocyanosis and abnormal pigmentation), blindness, osteoporosis, cerebellar ataxia, mitochondrial myopathy, deafness and diabetes mellitus.","definition_xrefs":["Orphanet:3390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome","secondary_identifiers":["OMIM:560000","UMLS:C3151959","MESH:C564014","MEDGEN:463309"],"synonyms":[{"name":"proximal tubulopathy, diabetes mellitus and cerebellar ataxia","type":"related"},{"name":"renal tubulopathy, diabetes mellitus, and cerebellar ataxia","type":"related"},{"name":"renal tubulopathy, diabetes mellitus, and cerebellar ataxia due to duplication of mitochondrial DNA","type":"related"}],"termid":"MONDO:0010798","xrefs":{"Monarch":{"xref_id":"0010798"}}}


id: PBO:0068934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 177, pseudogene","termid":"PBO:0068934"}


id: MONDO:0100279
data:
  {"annotated_genes":["SJAG_04146","SJAG_02788"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89009,89010],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013967"}]},"cv_name":"mondo","definition":"Any peroxisome biogenesis disorder in which the cause of the disease is a mutation in the PEX11B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Zellweger spectrum disorders","termid":"MONDO:0019609"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02788":null,"SJAG_04146":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019053"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559","MONDO:0005244","MONDO:0005066","MONDO:0019053"],"is_obsolete":false,"name":"peroxisome biogenesis disorder due to PEX11B defect","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"PEX11B related peroxisome biogenesis disorder","type":"exact"},{"name":"peroxisome biogenesis disorder due to PEX11B defect","type":"exact"}],"termid":"MONDO:0100279","terms_by_termid":{"MONDO:0013967":null},"xrefs":{"Monarch":{"xref_id":"0100279"}}}


id: GO:0000950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the catabolism of branched chain amino acids to produce branched chain alcohols with one carbon less than the starting amino acid. In S. cerevisiae, this is known to occur for leucine, isoleucine, valine, methionine, phenylalanine, tyrosine, or tryptophan. When a branched chain family amino acid, leucine, isoleucine, or valine, is used as the substrate, 3-methylbutanol, 2-methylbutanol, or 2-methylpropanol, respectively, is produced. Often referred to as the Ehrlich pathway, these reactions generally occur during fermentation to produce a variety of alcohols, often collectively referred to as fusel alcohols. Depending on the redox state of the cells, carboxylic acid derivatives may be produced instead of alcohols.","definition_xrefs":["GOC:krc","PMID:18281432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid catabolic process to alcohol via Ehrlich pathway","termid":"GO:0000947"},{"relation_name":"is_a","term_name":"branched-chain amino acid catabolic process","termid":"GO:0009083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"branched-chain amino acid catabolic process to alcohol via Ehrlich pathway","synonyms":[{"name":"branched chain family amino acid catabolic process to alcohol via Ehrlich pathway","type":"exact"}],"termid":"GO:0000950"}


id: PBO:0086369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative aminopeptidase; SWAT-GFP fusion protein localizes to the endoplasmic reticulum and vacuole, while mCherry fusion localizes to the vacuole","termid":"PBO:0086369"}


id: GO:0008113
data:
  {"annotated_genes":["SJAG_00419"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[61030],"is_not":false,"summary":null,"term":"GO:0008113"}]},"cv_name":"molecular_function","definition":"Catalysis of the reactions: peptide-L-methionine + thioredoxin disulfide + H2O = peptide-L-methionine (S)-S-oxide + thioredoxin, and L-methionine + thioredoxin disulfide + H2O = L-methionine (S)-S-oxide + thioredoxin. Can act on oxidized methionine in peptide linkage with specificity for the S enantiomer. Thioredoxin disulfide is the oxidized form of thioredoxin.","definition_xrefs":["GOC:mah","GOC:vw","PMID:11169920","EC:1.8.4.11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor","termid":"GO:0016671"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00419":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"peptide-methionine (S)-S-oxide reductase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["Reactome:R-HSA-5676940","GO:0033742","Reactome:R-HSA-1222363","RHEA:14217","GO:0072561","MetaCyc:RXN-8668"],"synonyms":[{"name":"MsrA","type":"related"},{"name":"methionine S-oxide reductase (S-form oxidizing) activity","type":"related"},{"name":"methionine S-oxide reductase activity","type":"broad"},{"name":"methionine sulfoxide (protein) reductase activity","type":"exact"},{"name":"methionine sulfoxide reductase A activity","type":"related"},{"name":"methionine sulfoxide reductase activity","type":"broad"},{"name":"methionine sulphoxide reductase A activity","type":"related"},{"name":"peptide Met(O) reductase activity","type":"related"},{"name":"peptide methionine sulfoxide reductase activity","type":"related"},{"name":"peptide-L-methionine:thioredoxin-disulfide S-oxidoreductase [L-methionine (S)-S-oxide-forming] activity","type":"related"},{"name":"peptide-methionine-(S)-S-oxide reductase activity","type":"exact"},{"name":"protein-methionine-S-oxide reductase activity","type":"exact"}],"termid":"GO:0008113","terms_by_termid":{"GO:0008113":null}}


id: PBO:0014306
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paroxysmal nocturnal haemoglobinuria","termid":"PBO:0014306"}


id: MONDO:0005544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Age-related neuropathological condition with severe neuronal cell loss and gliosis in the hippocampus","definition_xrefs":["EFO:0005678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral cortex disorder","termid":"MONDO:0044996"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hippocampal sclerosis of aging","secondary_identifiers":["UMLS:C5691287","MEDGEN:1801569"],"termid":"MONDO:0005544","xrefs":{"Monarch":{"xref_id":"0005544"}}}


id: PBO:0027636
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_RNA_level_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0027636"}


id: MONDO:8000023
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, primary immunodeficiency. It is caused by a currently undetermined defect in the Fas-induced apoptosis pathway. No mutations in Fas, FASLG or CASP10 are detectable. Disruption of Fas-induced apoptosis impairs lymphocyte homeostasis and immune tolerance. Characteristic laboratory findings include an increase in circulating, double-negative (CD4-/CD8-) T cells in the setting of immune-mediated anemia, thrombocytopenia and neutropenia. Clinical signs present in childhood include fatigue, pallor, bruising, hepatosplenomegaly and chronic, non-malignant, non-infectious lymphadenopathy. The clinical course is influenced by a strong association with other autoimmune disorders and an increased risk for developing Hodgkin and non-Hodgkin lymphoma.","definition_xrefs":["NCIT:C39577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune lymphoproliferative syndrome","termid":"MONDO:0017979"}],"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":"type 3 autoimmune lymphoproliferative syndrome","secondary_identifiers":["UMLS:C1519711","MEDGEN:274327"],"termid":"MONDO:8000023","xrefs":{"Monarch":{"xref_id":"8000023"}}}


id: PBO:0068274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease A family member 11 (inactive)","termid":"PBO:0068274"}


id: PBO:0061199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NOBOX oogenesis homeobox","termid":"PBO:0061199"}


id: PR:O13681
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ima1 gene.","definition_xrefs":["UniProtKB:O13681","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":"integral inner nuclear membrane protein ima1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC737.03c","synonyms":[{"name":"Spom972h-ima1","type":"exact"}],"termid":"PR:O13681"}


id: PBO:0078687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon AAG) 1-3","termid":"PBO:0078687"}


id: PR:C6Y4B3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pga1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4B3"],"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":"GPI mannosyltransferase 2 subunit C167.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC167.09","synonyms":[{"name":"Spom972h-pga1","type":"exact"}],"termid":"PR:C6Y4B3"}


id: GO:0005024
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a transforming growth factor beta (TGFbeta) and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity by catalysis of the reaction: ATP protein serine = ADP + protein serine phosphate, and ATP + protein threonine = ADP + protein threonine phosphate.","definition_xrefs":["GOC:mah","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane receptor protein serine/threonine kinase activity","termid":"GO:0004675"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0140096","GO:0016301","GO:0004672","GO:0003674","GO:0003824","GO:0016740","GO:0038023"],"is_obsolete":false,"name":"transforming growth factor beta receptor activity","synonyms":[{"name":"TGF-beta receptor activity","type":"exact"},{"name":"TGFbeta receptor activity","type":"exact"},{"name":"TGFbeta-activated receptor activity","type":"exact"},{"name":"TGFbetaR","type":"exact"},{"name":"transforming growth factor beta-activated receptor activity","type":"exact"}],"termid":"GO:0005024"}


id: GO:0016902
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of an oxidation-reduction (redox) reaction in which a CH-OH group acts as a hydrogen or electron donor and reduces an acceptor other than a cytochrome, disulfide, NAD, NADP, oxygen or a quinone or similar compound.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete oxidoreductase activity, acting on the CH-OH group of donors, other acceptors (obsolete GO:0016902)","synonyms":[{"name":"oxidoreductase activity, acting on the CH-OH group of donors, other acceptors","type":"exact"}],"termid":"GO:0016902"}


id: GO:0048491
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of synaptic vesicle along axonal microtubules from the presynapse to the cell body.","definition_xrefs":["PMID:24762653","GOC:jid","GOC:lmg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retrograde axonal transport","termid":"GO:0008090"},{"relation_name":"is_a","term_name":"synaptic vesicle transport along microtubule","termid":"GO:0099517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"retrograde synaptic vesicle transport","synonyms":[{"name":"retrograde axonal transport of synaptic vesicle","type":"exact"}],"termid":"GO:0048491"}


id: GO:0043177
data:
  {"annotated_genes":["SJAG_03861"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016594"}]},"cv_name":"molecular_function","definition":"Binding to an organic acid, any acidic compound containing carbon in covalent linkage.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule binding","termid":"GO:0036094"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03861":null},"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":"organic acid binding","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0043177","terms_by_termid":{"GO:0016594":null}}


id: PBO:0062677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 14 subfamily J member 1","termid":"PBO:0062677"}


id: MONDO:0011260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of pancreas lymphoma that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreas lymphoma","termid":"MONDO:0002114"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0004335"],"is_obsolete":false,"name":"pancreatic lymphoma, familial","secondary_identifiers":["OMIM:602596","UMLS:C1865139","MESH:C566516","MEDGEN:355383"],"synonyms":[{"name":"hereditary pancreas lymphoma","type":"exact"},{"name":"pancreatic lymphoma, familial","type":"exact"}],"termid":"MONDO:0011260","xrefs":{"Monarch":{"xref_id":"0011260"}}}


id: PBO:0060043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 31","termid":"PBO:0060043"}


id: MONDO:1012940
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hearing loss that occurs in dogs due to a mutation in the CDH23 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss disorder, non-human animal","termid":"MONDO:1012969"},{"relation_name":"is_a","term_name":"inherited auditory system disease, non-human animal","termid":"MONDO:1012970"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deafness, CDH23-related, dog","secondary_identifiers":["OMIA:002584-9615"],"termid":"MONDO:1012940","xrefs":{"Monarch":{"xref_id":"1012940"}}}


id: MONDO:1011883
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dilute coat color with neurological defects, non-human animal","secondary_identifiers":["OMIA:001501"],"termid":"MONDO:1011883","xrefs":{"Monarch":{"xref_id":"1011883"}}}


id: MONDO:0008430
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":"skeletal dysplasia with delayed epiphyseal and carpal bone ossification","secondary_identifiers":["OMIM:182255","UMLS:C1866939","MEDGEN:356650","MESH:C566687"],"synonyms":[{"name":"skeletal dysplasia with delayed epiphyseal and carpal bone ossification","type":"exact"}],"termid":"MONDO:0008430","xrefs":{"Monarch":{"xref_id":"0008430"}}}


id: PBO:0050964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon lambda receptor 1","termid":"PBO:0050964"}


id: MONDO:0005360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Dupuytren contracture (obsolete MONDO:0005360)","synonyms":[{"name":"obsolete Dupuytren contracture (disease)","type":"exact"}],"termid":"MONDO:0005360","xrefs":{"Monarch":{"xref_id":"0005360"}}}


id: PBO:0068119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 426","termid":"PBO:0068119"}


id: PBO:0035911
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_ubiquitination_during_vegetative_growth","termid":"PBO:0035911"}


id: PBO:0039271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldolase, fructose-bisphosphate C","termid":"PBO:0039271"}


id: MONDO:0008027
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":"muscular atrophy, malignant neurogenic","secondary_identifiers":["OMIM:158650","MEDGEN:322469","UMLS:C1834689","MESH:C563559"],"synonyms":[{"name":"muscular atrophy, malignant neurogenic","type":"exact"}],"termid":"MONDO:0008027","xrefs":{"Monarch":{"xref_id":"0008027"}}}


id: MONDO:0009478
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Combined immunodeficiency due to dedicator of cytokinesis 8 protein (DOCK8) deficiency is a form of T and B cell immunodeficiency characterized by recurrent cutaneous viral infections, susceptibility to cancer and elevated serum levels of immunoglobulin E (IgE).","definition_xrefs":["Orphanet:217390"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"hyper-IgE syndrome","termid":"MONDO:0018037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"combined immunodeficiency due to DOCK8 deficiency","secondary_identifiers":["OMIM:243700","UMLS:C4722305","NCIT:C126343","MEDGEN:1648410","DOID:0080594","GARD:2816","icd11.foundation:136043326"],"synonyms":[{"name":"AR hyperimmunoglobulin E syndrome","type":"related"},{"name":"AR-HIES","type":"related"},{"name":"Cid due to DOCK8 deficiency","type":"exact"},{"name":"DOCK8 deficiency","type":"related"},{"name":"DOCK8 immunodeficiency syndrome","type":"exact"},{"name":"HIES autosomal recessive","type":"related"},{"name":"HIES, autosomal recessive","type":"related"},{"name":"autosomal recessive hyper IgE syndrome","type":"related"},{"name":"combined immunodeficiency due to DOCK8 deficiency","type":"exact"},{"name":"combined immunodeficiency due to dedicator of cytokinesis 8 protein deficiency","type":"exact"},{"name":"dedicator of cytokinesis 8 deficiency","type":"exact"},{"name":"hyper Ig E syndrome, autosomal recessive","type":"related"},{"name":"hyper-IgE recurrent infection syndrome, autosomal recessive","type":"related"},{"name":"hyper-IgE syndrome, autosomal recessive","type":"related"},{"name":"hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive","type":"related"}],"termid":"MONDO:0009478","xrefs":{"Monarch":{"xref_id":"0009478"}}}


id: GO:1901942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of (+)-epi-alpha-bisabolol.","definition_xrefs":["PMID:22867794","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpenoid catabolic process","termid":"GO:0016107"},{"relation_name":"is_a","term_name":"(+)-epi-alpha-bisabolol metabolic process","termid":"GO:1901941"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"(+)-epi-alpha-bisabolol catabolic process","synonyms":[{"name":"(+)-epi-alpha-bisabolol breakdown","type":"exact"},{"name":"(+)-epi-alpha-bisabolol catabolism","type":"exact"},{"name":"(+)-epi-alpha-bisabolol degradation","type":"exact"}],"termid":"GO:1901942"}


id: PBO:0081498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 396","termid":"PBO:0081498"}


id: PBO:0030137
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_GTPase_activity","termid":"PBO:0030137"}


id: GO:1990843
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A mitochondrion that occurs adjacent to the sarcolemma in striated muscle cells and responds in distinct ways to physiological triggers.","definition_xrefs":["PMID:23297307","PMID:26039174"],"gene_count":0,"genotype_count":0,"name":"obsolete subsarcolemmal mitochondrion (obsolete GO:1990843)","synonyms":[{"name":"SS mitochondrion","type":"exact"},{"name":"SSM","type":"exact"}],"termid":"GO:1990843"}


id: SO:0001207
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region (DNA) to which the T7 RNA polymerase binds, to begin transcription.","definition_xrefs":["xenbase:jb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Phage_RNA_Polymerase_Promoter","termid":"SO:0001204"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T7_RNA_Polymerase_Promoter","synonyms":[{"name":"T7 RNA Polymerase Promoter","type":"exact"}],"termid":"SO:0001207"}


id: PBO:0086886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative transcription factor, contains Forkhead Associated domain; found associated with chromatin; target of SBF transcription factor; induced in response to DNA damaging agents and deletion of telomerase; PLM2 has a paralog, TOS4, that arose from the whole genome duplication","termid":"PBO:0086886"}


id: PBO:0053663
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 840","termid":"PBO:0053663"}


id: GO:0140649
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directional movement of a hyphal filament from one host cell to another. This process involves the clearance of plant-derived plasmodesmal occlusion materials, cytoskeleton based constriction of invasive hypha to traverse plasmodesmata. Septins and F-actin are reorganized into an hourglass shape at the point of maximum hyphal constriction.","definition_xrefs":["PMID:29567712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated cell-to-cell migration in host","termid":"GO:0106259"}],"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":"symbiont-mediated cell-to-cell migration by invasive hypha","synonyms":[{"name":"cell-to-cell migration by invasive hypha","type":"exact"},{"name":"host tissue colonization","type":"broad"},{"name":"invasive growth","type":"broad"},{"name":"invasive hyphae formation","type":"exact"},{"name":"plant tissue colonization","type":"broad"}],"termid":"GO:0140649"}


id: GO:0050001
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + L-glutamine = NH3 + D-glutamate.","definition_xrefs":["EC:3.5.1.35","MetaCyc:D-GLUTAMINASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0016810","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"D-glutaminase activity","secondary_identifiers":["RHEA:22840"],"synonyms":[{"name":"D-glutamine amidohydrolase activity","type":"related"}],"termid":"GO:0050001"}


id: GO:0097619
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that acts as a protein trafficking machinery and is responsible for the export of proteins across the parasitophorous (symbiont-containing) vacuolar membrane and into the human host cell. The PTEX complex is located in the vacuole membrane. It is ATP-powered, and comprises heat shock protein 101 (HSP101; a ClpA/B-like ATPase from the AAA+ superfamily, of a type commonly associated with protein translocons), a parasite protein termed PTEX150, and exported protein 2 (EXP2). EXP2 is the potential channel, as it is the membrane-associated component of the core PTEX complex. Two other proteins, PTEX88 and thioredoxin 2 (TRX2), were also identified as PTEX components.","definition_xrefs":["PMID:25043043","PMID:19536257","GOC:pr","PMID:25043010"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"symbiont-containing vacuole membrane","termid":"GO:0020005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"PTEX complex","synonyms":[{"name":"Plasmodium translocon of exported proteins","type":"related"}],"termid":"GO:0097619"}


id: MONDO:0015792
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A common, self-limiting thyroid disorder seen in preterm infants that is characterized by abnormally low serum levels of thyroxine and free thyroxine with normal serum levels of thyroid stimulating hormone.","definition_xrefs":["NCIT:C113171"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypothyroidism","termid":"MONDO:0018612"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transient congenital hypothyroidism","secondary_identifiers":["Orphanet:178045","UMLS:C3827793","GARD:20142","SCTID:119181000119104","icd11.foundation:592246939","MEDGEN:820541"],"synonyms":[{"name":"THOP","type":"exact"},{"name":"hypothyroxinemia of prematurity","type":"exact"},{"name":"transient hypothyroxinemia of prematurity","type":"exact"}],"termid":"MONDO:0015792","xrefs":{"Monarch":{"xref_id":"0015792"}}}


id: PBO:0044614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDB1 and CUL4 associated factor 16","termid":"PBO:0044614"}


id: PR:P24488
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- php2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P24488"],"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":"transcriptional activator hap2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC725.11c","synonyms":[{"name":"Spom972h-php2","type":"exact"}],"termid":"PR:P24488"}


id: FYPO:0008398
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the level of cell damage is abnormal.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process","termid":"FYPO:0000628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal level of cell damage","termid":"FYPO:0008398"}


id: PBO:0062061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily Y member 1","termid":"PBO:0062061"}


id: PBO:0045415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmental pluripotency associated 5","termid":"PBO:0045415"}


id: PBO:0005418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-DBF type","termid":"PBO:0005418"}


id: PBO:0109111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase 2A, tRNA N3-cytidine","termid":"PBO:0109111"}


id: PBO:0073891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 12 member 7","termid":"PBO:0073891"}


id: PBO:0017413
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-precedes","termid":"PBO:0017413"}


id: GO:0005610
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A laminin complex composed of alpha3, beta3 and gamma2 polypeptide chains.","definition_xrefs":["GOC:jl","PMID:10842354"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laminin complex","termid":"GO:0043256"}],"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":"laminin-5 complex","synonyms":[{"name":"laminin-332 complex","type":"narrow"},{"name":"laminin-3A32 complex","type":"exact"},{"name":"laminin-5A complex","type":"exact"}],"termid":"GO:0005610"}


id: PBO:0053362
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 269","termid":"PBO:0053362"}


id: PBO:0065414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit beta 3","termid":"PBO:0065414"}


id: PATO:0001790
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A density which is lower relative to the normal or average.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"dense","termid":"PATO:0001164"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased mass density","synonyms":[{"name":"low density","type":"exact"}],"termid":"PATO:0001790"}


id: GO:0008171
data:
  {"annotated_genes":["SJAG_00722","SJAG_03332","SJAG_01269","SJAG_03773","SJAG_02660","SJAG_00559","SJAG_02817","SJAG_04642","SJAG_01375","SJAG_05016"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[66231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061542"},{"annotations":[116854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120537"},{"annotations":[77913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018423"},{"annotations":[77196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004671"},{"annotations":[109976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990276"},{"annotations":[91453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070039"},{"annotations":[77697,77452,80512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008650"},{"annotations":[111066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090486"},{"annotations":[60904,99727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106050"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a methyl group to the oxygen atom of an acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00559":null,"SJAG_00722":null,"SJAG_01269":null,"SJAG_01375":null,"SJAG_02660":null,"SJAG_02817":null,"SJAG_03332":null,"SJAG_03773":null,"SJAG_04642":null,"SJAG_05016":null},"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:0016741"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016741"],"is_obsolete":false,"name":"O-methyltransferase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5578717","Reactome:R-HSA-5629237","Reactome:R-HSA-5629218","Reactome:R-HSA-5629203","Reactome:R-HSA-6790907"],"termid":"GO:0008171","terms_by_termid":{"GO:0004671":null,"GO:0008650":null,"GO:0018423":null,"GO:0061542":null,"GO:0070039":null,"GO:0090486":null,"GO:0106050":null,"GO:0120537":null,"GO:1990276":null}}


id: GO:0061285
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the mesonephric capsule over time, from its formation to the mature structure. The mesonephric capsule is the tough fibrous layer surrounding the mesonephros, covered in a thick layer of perinephric adipose tissue.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal capsule development","termid":"GO:0072127"},{"relation_name":"part_of","term_name":"mesonephros development","termid":"GO:0001823"}],"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":"mesonephric capsule development","termid":"GO:0061285"}


id: GO:2000144
data:
  {"annotated_genes":["SJAG_00909","SJAG_00766","SJAG_04099","SJAG_04820","SJAG_01403","SJAG_03622","SJAG_03421","SJAG_04705","SJAG_01952","SJAG_05203","SJAG_00342","SJAG_02849","SJAG_02494","SJAG_00150","SJAG_03590","SJAG_02391","SJAG_03573","SJAG_02551","SJAG_05341","SJAG_00297","SJAG_04647","SJAG_01771","SJAG_00904"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91533,81360],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045899"},{"annotations":[92506,100549,96298,100902,65352,97243,105316,108299,107615,89256,105576,110695,97725,110668,103852,96183,92191,107972,108162,116712,120944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060261"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of DNA-templated transcription initiation.","definition_xrefs":["GOC:mah","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA-templated transcription","termid":"GO:0045893"},{"relation_name":"is_a","term_name":"regulation of DNA-templated transcription initiation","termid":"GO:2000142"},{"relation_name":"positively_regulates","term_name":"DNA-templated transcription initiation","termid":"GO:0006352"}],"gene_count":23,"genes_by_uniquename":{"SJAG_00150":null,"SJAG_00297":null,"SJAG_00342":null,"SJAG_00766":null,"SJAG_00904":null,"SJAG_00909":null,"SJAG_01403":null,"SJAG_01771":null,"SJAG_01952":null,"SJAG_02391":null,"SJAG_02494":null,"SJAG_02551":null,"SJAG_02849":null,"SJAG_03421":null,"SJAG_03573":null,"SJAG_03590":null,"SJAG_03622":null,"SJAG_04099":null,"SJAG_04647":null,"SJAG_04705":null,"SJAG_04820":null,"SJAG_05203":null,"SJAG_05341":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"positively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006355","GO:0006351","GO:0010467"],"is_obsolete":false,"name":"positive regulation of DNA-templated transcription initiation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"positive regulation of DNA-dependent transcription, initiation","type":"exact"},{"name":"positive regulation of DNA-templated transcription, initiation","type":"exact"},{"name":"positive regulation of initiation of DNA-dependent transcription","type":"exact"},{"name":"positive regulation of transcription initiation, DNA-dependent","type":"exact"},{"name":"transactivation","type":"related"},{"name":"transcriptional transactivation","type":"related"}],"termid":"GO:2000144","terms_by_termid":{"GO:0045899":null,"GO:0060261":null}}


id: MONDO:0021321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the extrahepatic bile duct.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bile duct cancer","termid":"MONDO:0003059"},{"relation_name":"is_a","term_name":"extrahepatic bile duct neoplasm","termid":"MONDO:0021385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992","MONDO:0002515"],"is_obsolete":false,"name":"malignant tumor of extrahepatic bile duct","secondary_identifiers":["SCTID:363416002","NCIT:C7483","MEDGEN:56304","UMLS:C0153453","ICD9:156.8","ICD9:156.1"],"synonyms":[{"name":"cancer of extrahepatic bile duct","type":"exact"},{"name":"extrahepatic bile duct cancer","type":"broad"},{"name":"malignant extrahepatic bile duct neoplasm","type":"exact"},{"name":"malignant extrahepatic bile duct tumor","type":"exact"},{"name":"malignant extrahepatic bile duct tumour","type":"exact"},{"name":"malignant neoplasm of extrahepatic bile duct","type":"exact"},{"name":"malignant neoplasm of the extrahepatic bile duct","type":"exact"},{"name":"malignant tumor of the extrahepatic bile duct","type":"exact"},{"name":"malignant tumour of the extrahepatic bile duct","type":"exact"}],"termid":"MONDO:0021321","xrefs":{"Monarch":{"xref_id":"0021321"}}}


id: PBO:0049709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan synthase 3","termid":"PBO:0049709"}


id: GO:0099120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a non-reproductive fruiting body over time, from its formation to the mature structure. A non-reproductive fruiting body is a colonial multicellular structure consisting of co-operating unicellular organisms, some of which are spores. An example of such a process is found in Dictyostelium discoideum and Myxococcus xanthus colonies.","definition_xrefs":["PMID:12448714","GOC:pf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"is_a","term_name":"biological process involved in intraspecies interaction between organisms","termid":"GO:0051703"}],"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":"socially cooperative development","secondary_identifiers":["GO:0090702"],"synonyms":[{"name":"colonial development","type":"exact"},{"name":"non-reproductive fruiting body development","type":"related"},{"name":"socially co-operative development","type":"exact"}],"termid":"GO:0099120"}


id: MONDO:0005115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A localization-related (focal) form of epilepsy characterized by recurrent seizures that arise from foci within the temporal lobe, most commonly from its mesial aspect. A wide variety of psychic phenomena may be associated, including illusions, hallucinations, dyscognitive states, and affective experiences. The majority of complex partial seizures (see epilepsy, complex partial) originate from the temporal lobes. Temporal lobe seizures may be classified by etiology as cryptogenic, familial, or symptomatic (i.e., related to an identified disease process or lesion). (From Adams et al., Principles of Neurology, 6th ed, p321)","definition_xrefs":["MESH:D004833"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial partial epilepsy","termid":"MONDO:0017704"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"temporal lobe epilepsy","secondary_identifiers":["SCTID:783739005","OMIMPS:600512","UMLS:C0014556","NCIT:C177244","DOID:3328","GARD:5135","SCTID:193000002","MEDGEN:4990","Orphanet:98819","NIFSTD:birnlex_12733","EFO:0000773"],"synonyms":[{"name":"epilepsy of temporal lobe","type":"exact"},{"name":"epilepsy, familial temporal lobe","type":"exact"},{"name":"epilepsy, temporal lobe","type":"exact"},{"name":"familial temporal lobe epilepsy syndrome","type":"exact"},{"name":"temporal lobe epilepsy","type":"exact"}],"termid":"MONDO:0005115","xrefs":{"Monarch":{"xref_id":"0005115"}}}


id: PBO:0074404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 10 like 2B","termid":"PBO:0074404"}


id: MONDO:0002838
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spindle cell carcinoma (obsolete MONDO:0002838)","termid":"MONDO:0002838","xrefs":{"Monarch":{"xref_id":"0002838"}}}


id: GO:0050439
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + glyoxylate + H+ = 2-hydroxy-3-oxoadipate + CO2.","definition_xrefs":["RHEA:14341","EC:2.2.1.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transketolase or transaldolase activity","termid":"GO:0016744"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016744"}],"interesting_parent_ids":["GO:0016744","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"2-hydroxy-3-oxoadipate synthase activity","secondary_identifiers":["MetaCyc:2-HYDROXY-3-OXOADIPATE-SYNTHASE-RXN","KEGG_REACTION:R00474"],"synonyms":[{"name":"2-hydroxy-3-oxoadipate glyoxylate-lyase (carboxylating) activity","type":"related"},{"name":"2-hydroxy-3-oxoadipate synthetase activity","type":"related"},{"name":"2-oxoglutarate:glyoxylate succinaldehydetransferase (decarboxylating)","type":"related"},{"name":"alpha-ketoglutaric-glyoxylic carboligase activity","type":"related"},{"name":"oxoglutarate: glyoxylate carboligase activity","type":"related"},{"name":"oxoglutarate:glyoxylate carboligase activity","type":"related"}],"termid":"GO:0050439"}


id: GO:0004984
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an odorant and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity in response to detection of smell.","definition_xrefs":["PMID:21041441","GOC:sart","GOC:bf","GOC:dph","PMID:19135896"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"olfactory receptor activity","synonyms":[{"name":"odorant receptor activity","type":"exact"}],"termid":"GO:0004984"}


id: GO:1903006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein K63-linked deubiquitination.","definition_xrefs":["GOC:bf","GO_REF:0000058","GOC:PARL","GOC:TermGenie","PMID:22970133"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein deubiquitination","termid":"GO:1903003"},{"relation_name":"is_a","term_name":"regulation of protein K63-linked deubiquitination","termid":"GO:1903004"},{"relation_name":"positively_regulates","term_name":"protein K63-linked deubiquitination","termid":"GO:0070536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"positively_regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0008150","GO:0070647"],"is_obsolete":false,"name":"positive regulation of protein K63-linked deubiquitination","synonyms":[{"name":"activation of protein K63-linked deubiquitination","type":"narrow"},{"name":"up regulation of protein K63-linked deubiquitination","type":"exact"},{"name":"up-regulation of protein K63-linked deubiquitination","type":"exact"},{"name":"upregulation of protein K63-linked deubiquitination","type":"exact"}],"termid":"GO:1903006"}


id: PBO:0077530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 243","termid":"PBO:0077530"}


id: PBO:0029817
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,_single_cell_division,_abnormal_cell_shape","termid":"PBO:0029817"}


id: PBO:0079502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin like 4B","termid":"PBO:0079502"}


id: PBO:0085340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphoinositide binding protein; required for vesicle formation in the cytoplasm-to-vacuole targeting (CVT) pathway, autophagy, micronucleophagy and mitophagy; binds to several phosphoinositides including: PtdIns(3,5)P2, PI3P and PI4P; involved in PI3P-dependent recruitment and organization of both the Atg12-Atg5-Atg16 complex and Atg8p at the pre-autophagosomal structure; necessary for oxidant-induced cell death; WD-40 repeat containing PROPPIN family member","termid":"PBO:0085340"}


id: PBO:0004057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell surface agglutination protein Map4","termid":"PBO:0004057"}


id: GO:0002108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the maturation of a precursor Large SubUnit (LSU) ribosomal RNA (rRNA) molecule into a mature LSU-rRNA molecule from the pre-rRNA molecule originally produced as a tricistronic rRNA transcript that contains the Small Subunit (SSU) rRNA, Large Subunit (LSU) the 5S rRNA in that order from 5' to 3' along the primary transcript.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maturation of LSU-rRNA","termid":"GO:0000470"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0010467","GO:0042254","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, LSU-rRNA,5S)","termid":"GO:0002108"}


id: PBO:0030705
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_4-nitroquinoline_N-oxide","termid":"PBO:0030705"}


id: PBO:0082639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of glutamine amidotransferase (GATase II); forms a complex with Dug3p to degrade glutathione (GSH) and other peptides containing a gamma-glu-X bond in an alternative pathway to GSH degradation by gamma-glutamyl transpeptidase (Ecm38p)","termid":"PBO:0082639"}


id: PBO:0078070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 60 (pseudogene)","termid":"PBO:0078070"}


id: PBO:0058059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4280","termid":"PBO:0058059"}


id: GO:0047905
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-fructose 6-phosphate + phosphate = acetyl phosphate + D-erythrose 4-phosphate + H2O.","definition_xrefs":["EC:4.1.2.22","MetaCyc:FRUCTOSE-6-PHOSPHATE-PHOSPHOKETOLASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"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:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"fructose-6-phosphate phosphoketolase activity","secondary_identifiers":["RHEA:12196"],"synonyms":[{"name":"D-fructose-6-phosphate D-erythrose-4-phosphate-lyase (adding phosphate; acetyl-phosphate-forming)","type":"related"},{"name":"D-fructose-6-phosphate D-erythrose-4-phosphate-lyase (phosphate-acetylating) activity","type":"related"}],"termid":"GO:0047905"}


id: PBO:0031366
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_2-deoxyglucose","termid":"PBO:0031366"}


id: MONDO:1011133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pneumothorax that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pneumothorax, non-human animal","termid":"MONDO:1010286"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pneumothorax, dog","secondary_identifiers":["OMIA:000804-9615"],"termid":"MONDO:1011133","xrefs":{"Monarch":{"xref_id":"1011133"}}}


id: GO:0042096
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete alpha-beta T cell receptor activity (obsolete GO:0042096)","synonyms":[{"name":"alpha-beta T cell receptor activity","type":"exact"}],"termid":"GO:0042096"}


id: MONDO:0001557
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A bursitis that involves the olecranon.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enthesopathy","termid":"MONDO:0002183"},{"relation_name":"is_a","term_name":"bursitis","termid":"MONDO:0002471"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olecranon bursitis","secondary_identifiers":["MEDGEN:538225","SCTID:425940002","DOID:12581","ICD10CM:M70.2","ICD9:726.33","UMLS:C0263962"],"synonyms":[{"name":"Miners' elbow","type":"exact"},{"name":"bursitis of elbow","type":"exact"},{"name":"bursitis of elbow region","type":"exact"},{"name":"bursitis of olecranon","type":"exact"},{"name":"capped elbow","type":"exact"},{"name":"elbow bursitis","type":"exact"},{"name":"elbow bursitis (& olecranon)","type":"exact"},{"name":"miner's elbow","type":"exact"},{"name":"olecranon bursitis","type":"exact"},{"name":"shoe boil","type":"exact"}],"termid":"MONDO:0001557","xrefs":{"Monarch":{"xref_id":"0001557"}}}


id: PBO:0028772
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_L-methionine_(R)-S-oxide","termid":"PBO:0028772"}


id: GO:0022803
data:
  {"annotated_genes":["SJAG_02019","SJAG_MIT09","SJAG_MIT37","SJAG_05229","SJAG_01090","SJAG_05342","SJAG_04731","SJAG_00133","SJAG_00048","SJAG_03925","SJAG_02532","SJAG_03895","SJAG_00985","SJAG_MIT15","SJAG_04471","SJAG_02598","SJAG_02322","SJAG_04136","SJAG_02105","SJAG_00836","SJAG_05204","SJAG_03114","SJAG_07003","SJAG_00438","SJAG_00915","SJAG_04668","SJAG_00542","SJAG_04122","SJAG_01168","SJAG_02564","SJAG_02877"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77124,71564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008519"},{"annotations":[74172,79033,116417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005262"},{"annotations":[74790,81627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005227"},{"annotations":[72154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005254"},{"annotations":[76209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008331"},{"annotations":[105669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140135"},{"annotations":[97545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008381"},{"annotations":[121088,121081,96705,71623,77585,57995,79590,71916,109838,74492,81112,121075,95715,79914,95124,109746,103716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046933"},{"annotations":[94189,94247,101510,115901],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015275"},{"annotations":[73435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008308"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a single solute from one side of a membrane to the other by a mechanism involving conformational change, either by facilitated diffusion or in a membrane potential dependent process if the solute is charged.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":31,"genes_by_uniquename":{"SJAG_00048":null,"SJAG_00133":null,"SJAG_00438":null,"SJAG_00542":null,"SJAG_00836":null,"SJAG_00915":null,"SJAG_00985":null,"SJAG_01090":null,"SJAG_01168":null,"SJAG_02019":null,"SJAG_02105":null,"SJAG_02322":null,"SJAG_02532":null,"SJAG_02564":null,"SJAG_02598":null,"SJAG_02877":null,"SJAG_03114":null,"SJAG_03895":null,"SJAG_03925":null,"SJAG_04122":null,"SJAG_04136":null,"SJAG_04471":null,"SJAG_04668":null,"SJAG_04731":null,"SJAG_05204":null,"SJAG_05229":null,"SJAG_05342":null,"SJAG_07003":null,"SJAG_MIT09":null,"SJAG_MIT15":null,"SJAG_MIT37":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"passive transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0022814","Wikipedia:Facilitated_diffusion"],"synonyms":[{"name":"facilitated diffusion","type":"related"},{"name":"porters","type":"broad"},{"name":"uniporter activity z","type":"narrow"}],"termid":"GO:0022803","terms_by_termid":{"GO:0005227":null,"GO:0005254":null,"GO:0005262":null,"GO:0008308":null,"GO:0008331":null,"GO:0008381":null,"GO:0008519":null,"GO:0015275":null,"GO:0046933":null,"GO:0140135":null}}


id: PBO:0078525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 16","termid":"PBO:0078525"}


id: FYPO:0002015
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 cells show increased sensitivity to iron ion starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to stress during vegetative growth","termid":"FYPO:0000304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000139","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to iron ion starvation","synonyms":[{"name":"decreased growth during cellular response to iron ion starvation","type":"exact"},{"name":"decreased vegetative cell population growth during cellular response to iron ion starvation","type":"exact"},{"name":"hypersensitive to iron ion starvation","type":"exact"},{"name":"sensitive to iron ion depletion","type":"exact"},{"name":"sensitive to iron ion deprivation","type":"exact"},{"name":"sensitive to iron ion starvation during mitotic cell cycle","type":"related"},{"name":"sensitive to iron ion starvation during vegetative growth","type":"exact"},{"name":"sensitive to iron starvation","type":"exact"}],"termid":"FYPO:0002015"}


id: PBO:0034355
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increases_expression_of","termid":"PBO:0034355"}


id: PBO:0085148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleoporin involved in nucleocytoplasmic transport; binds to either the nucleoplasmic or cytoplasmic faces of the nuclear pore complex depending on Ran-GTP levels; also has a role in chromatin organization","termid":"PBO:0085148"}


id: GO:0032586
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a protein storage vacuole.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant-type vacuole membrane","termid":"GO:0009705"},{"relation_name":"part_of","term_name":"protein storage vacuole","termid":"GO:0000326"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005773","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"protein storage vacuole membrane","termid":"GO:0032586"}


id: FYPO:0003344
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed when a cell population is in stationary phase in which a cell is elongated, has two or more nuclei and more than one septum, and the septa not grouped together, but are located so as to form separate compartments with a single nucleus in each.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated multinucleate multiseptate cell, single septa between nuclei","termid":"FYPO:0003343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0000631","FYPO:0000005","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"elongated multinucleate multiseptate cell, single septa between nuclei, during stationary phase","synonyms":[{"name":"elongated multinucleate multiseptate cell, single septa between nuclei during stationary phase","type":"exact"},{"name":"elongated multinucleate multiseptate cell, single septa between nuclei, during stationary phase during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003344"}


id: GO:0044293
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Small dendrites that makes up a brush structure found as the terminal specialization of a dendrite of a unipolar brush cell (UBC).","definition_xrefs":["PMID:8300904","GOC:jl","NIF_Subcellular:sao28175134","NIF_Subcellular:sao295057932"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite terminus","termid":"GO:0044292"}],"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":"dendriole","termid":"GO:0044293"}


id: GO:0102482
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-deoxy-D-glucuronate = 5-dehydro-2-deoxy-D-gluconate.","definition_xrefs":["RHEA:25840","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"5-deoxy-D-glucuronate isomerase activity","secondary_identifiers":["MetaCyc:RXN-14150","EC:5.3.1.30"],"termid":"GO:0102482"}


id: PBO:0054725
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 2134","termid":"PBO:0054725"}


id: PR:Q09813
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- taf111 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09813"],"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":"transcription initiation factor TFIID 111 kDa subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2G11.14","synonyms":[{"name":"Spom972h-taf111","type":"exact"},{"name":"TAFII-111 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"TBP-associated factor 111 kDa (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09813"}


id: GO:0032277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the regulated release of a gonadotropin.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gonadotropin secretion","termid":"GO:0032276"},{"relation_name":"is_a","term_name":"negative regulation of hormone secretion","termid":"GO:0046888"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"gonadotropin secretion","termid":"GO:0032274"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of gonadotropin secretion","synonyms":[{"name":"down regulation of gonadotropin secretion","type":"exact"},{"name":"down-regulation of gonadotropin secretion","type":"exact"},{"name":"downregulation of gonadotropin secretion","type":"exact"},{"name":"inhibition of gonadotropin secretion","type":"narrow"},{"name":"negative regulation of gonadotrophin secretion","type":"exact"}],"termid":"GO:0032277"}


id: MONDO:0008824
data:
  {"annotated_genes":["SJAG_01065"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100104"}]},"cv_name":"mondo","definition":"Fetal akinesia deformation sequence (FADS) is a condition characterized by decreased fetal movement (fetal akinesia) as well as intra-uterine growth restriction (IUGR), multiple joint contractures (arthrogryposis), facial anomalies, underdevelopment of the lungs (pulmonary hypoplasia) and other developmental abnormalities. It is generally accepted that this condition is not a true diagnosis or a specific syndrome, but rather a description of a group of abnormalities resulting from fetal akinesia. About 30% of affected individuals are stillborn; many liveborn infants survive only a short time due to complications of pulmonary hypoplasia. FADS may be inherited in an autosomal recessive manner in some cases and may sometimes be caused by mutations in the RAPSN or DOK7 genes.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic respiratory or mediastinal malformation (obsolete MONDO:0015221)","termid":"MONDO:0015221"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"},{"relation_name":"is_a","term_name":"thoracic malformation","termid":"MONDO:0015929"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01065":null},"genotype_count":0,"is_obsolete":false,"name":"fetal akinesia deformation sequence","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:754.89","DOID:0111375","MESH:C536647","GARD:9634","NCIT:C129071","OMIMPS:208150","SCTID:401138005"],"synonyms":[{"name":"FADS","type":"exact"},{"name":"arthrogryposis multiplex congenita with pulmonary hypoplasia","type":"related"},{"name":"arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome","type":"exact"},{"name":"fetal akinesia deformation sequence","type":"exact"},{"name":"fetal akinesia sequence","type":"related"},{"name":"foetal akinesia sequence","type":"related"}],"termid":"MONDO:0008824","terms_by_termid":{"MONDO:0100104":null},"xrefs":{"Monarch":{"xref_id":"0008824"}}}


id: GO:0010638
data:
  {"annotated_genes":["SJAG_03438","SJAG_02342","SJAG_04776","SJAG_05289","SJAG_04597","SJAG_01212","SJAG_02433","SJAG_02380","SJAG_00666","SJAG_04312","SJAG_00082","SJAG_02169","SJAG_04968","SJAG_01805","SJAG_03631","SJAG_02498","SJAG_03126","SJAG_03137","SJAG_02336","SJAG_03812","SJAG_00266","SJAG_03048","SJAG_03681","SJAG_01837","SJAG_04573","SJAG_00718","SJAG_03353","SJAG_04259","SJAG_03957","SJAG_03624","SJAG_02592","SJAG_01297","SJAG_02990","SJAG_02332","SJAG_00142","SJAG_00823","SJAG_03581","SJAG_01679","SJAG_00883","SJAG_02451","SJAG_03851","SJAG_03936"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010846"},{"annotations":[92549,109161,110193,113924,101468,105796,115755,116248,117883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[96044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[110505,110598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000786"},{"annotations":[99498],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901098"},{"annotations":[65651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903373"},{"annotations":[100841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031453"},{"annotations":[104273,118660,91474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905561"},{"annotations":[103747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031117"},{"annotations":[97607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090297"},{"annotations":[110827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090141"},{"annotations":[91822,96258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903501"},{"annotations":[115333,96436,112479,89337,96259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903473"},{"annotations":[104277,118662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903380"},{"annotations":[99572,113337,95649,104003,104278,116748,102027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045842"},{"annotations":[96260,91825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902846"},{"annotations":[113398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110161"},{"annotations":[93017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090053"},{"annotations":[90883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010845"},{"annotations":[96220,112297,93018],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090055"},{"annotations":[109341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045876"},{"annotations":[99057],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032215"},{"annotations":[112219,99499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061191"}]},"cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of a process involved in the formation, arrangement of constituent parts, or disassembly of an organelle.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organelle organization","termid":"GO:0033043"},{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"positively_regulates","term_name":"organelle organization","termid":"GO:0006996"}],"gene_count":42,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00142":null,"SJAG_00266":null,"SJAG_00666":null,"SJAG_00718":null,"SJAG_00823":null,"SJAG_00883":null,"SJAG_01212":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02380":null,"SJAG_02433":null,"SJAG_02451":null,"SJAG_02498":null,"SJAG_02592":null,"SJAG_02990":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03137":null,"SJAG_03353":null,"SJAG_03438":null,"SJAG_03581":null,"SJAG_03624":null,"SJAG_03631":null,"SJAG_03681":null,"SJAG_03812":null,"SJAG_03851":null,"SJAG_03936":null,"SJAG_03957":null,"SJAG_04259":null,"SJAG_04312":null,"SJAG_04573":null,"SJAG_04597":null,"SJAG_04776":null,"SJAG_04968":null,"SJAG_05289":null},"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 organelle organization","references_by_uniquename":{"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"positive regulation of organelle organisation","type":"exact"},{"name":"positive regulation of organelle organization and biogenesis","type":"related"}],"termid":"GO:0010638","terms_by_termid":{"GO:0010845":null,"GO:0010846":null,"GO:0031117":null,"GO:0031453":null,"GO:0032215":null,"GO:0045842":null,"GO:0045876":null,"GO:0061191":null,"GO:0090053":null,"GO:0090055":null,"GO:0090141":null,"GO:0090297":null,"GO:0110161":null,"GO:0140499":null,"GO:1901098":null,"GO:1902426":null,"GO:1902846":null,"GO:1903373":null,"GO:1903380":null,"GO:1903473":null,"GO:1903501":null,"GO:1905561":null,"GO:2000786":null}}


id: PBO:0064605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POU class 3 homeobox 3","termid":"PBO:0064605"}


id: GO:0031045
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Electron-dense organelle with a granular internal matrix; contains proteins destined to be secreted.","definition_xrefs":["NIF_Subcellular:sao772007592","PMID:14690495"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule","termid":"GO:0030141"}],"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":"is_a","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0031410","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"dense core granule","synonyms":[{"name":"dense core vesicle","type":"exact"}],"termid":"GO:0031045"}


id: GO:0030098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized precursor cell acquires specialized features of a lymphocyte. A lymphocyte is a leukocyte commonly found in the blood and lymph that has the characteristics of a large nucleus, a neutral staining cytoplasm, and prominent heterochromatin.","definition_xrefs":["CL:0000542","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphocyte activation","termid":"GO:0046649"},{"relation_name":"is_a","term_name":"mononuclear cell differentiation","termid":"GO:1903131"}],"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":"lymphocyte differentiation","secondary_identifiers":["GO:0046650"],"synonyms":[{"name":"lymphocyte cell differentiation","type":"exact"},{"name":"lymphocyte development","type":"related"},{"name":"lymphocytic blood cell differentiation","type":"exact"}],"termid":"GO:0030098"}


id: FYPO:0005661
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which transcription occurs to a greater extent than normal when the cell is subject to nitrogen starvation. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription","termid":"FYPO:0002875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0006551"],"is_obsolete":false,"name":"increased transcription during nitrogen starvation","synonyms":[{"name":"increased transcription during cellular response to nitrogen starvation","type":"exact"},{"name":"increased transcription during nitrogen depletion","type":"exact"},{"name":"increased transcription during nitrogen deprivation","type":"exact"},{"name":"increased transcription during nitrogen limitation","type":"exact"},{"name":"increased transcription in response to nitrogen starvation","type":"exact"},{"name":"increased transcriptional response to nitrogen starvation","type":"exact"}],"termid":"FYPO:0005661"}


id: PBO:0070583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 49","termid":"PBO:0070583"}


id: PBO:0062073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily A member 4 pseudogene","termid":"PBO:0062073"}


id: GO:0072114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the pronephros are generated and organized. In mammals, the pronephros is the first of the three embryonic kidneys to be established and exists only transiently. In lower vertebrates such as fish and amphibia, the pronephros is the fully functional embryonic kidney and is indispensable for larval life.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney morphogenesis","termid":"GO:0060993"},{"relation_name":"part_of","term_name":"pronephros development","termid":"GO:0048793"}],"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":"pronephros morphogenesis","synonyms":[{"name":"pronephric kidney morphogenesis","type":"exact"}],"termid":"GO:0072114"}


id: MONDO:0012583
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tooth agenesis","termid":"MONDO:0005486"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tooth agenesis, selective, 5","secondary_identifiers":["GARD:18248","UMLS:C1858210","MEDGEN:346764","MESH:C565757","OMIM:610926"],"synonyms":[{"name":"STHAG5","type":"exact"},{"name":"he-Zhao deficiency","type":"related"},{"name":"hypodontia/oligodontia 5","type":"related"},{"name":"tooth agenesis, selective, 5","type":"exact"}],"termid":"MONDO:0012583","xrefs":{"Monarch":{"xref_id":"0012583"}}}


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:25832476","PMID:31399790"],"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: GO:0008715
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: CDP-diacylglycerol + H2O = a phosphatidate + CMP + 2 H+.","definition_xrefs":["EC:3.6.1.26","RHEA:15221"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"CDP-diacylglycerol diphosphatase activity","secondary_identifiers":["MetaCyc:CDPDIGLYPYPHOSPHA-RXN","KEGG_REACTION:R01797"],"synonyms":[{"name":"CDP diacylglycerol hydrolase activity","type":"related"},{"name":"CDP-diacylglycerol phosphatidylhydrolase activity","type":"related"},{"name":"CDP-diacylglycerol pyrophosphatase activity","type":"exact"},{"name":"cytidine diphosphodiacylglycerol pyrophosphatase activity","type":"related"}],"termid":"GO:0008715"}


id: MONDO:0014916
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC1A2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early myoclonic encephalopathy","termid":"MONDO:0016022"},{"relation_name":"is_a","term_name":"undetermined early-onset epileptic encephalopathy","termid":"MONDO:0018614"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066","MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 41","secondary_identifiers":["OMIM:617105","DOID:0080442","MEDGEN:934684","UMLS:C4310717","GARD:16190"],"synonyms":[{"name":"DEE41","type":"exact"},{"name":"EIEE41","type":"exact"},{"name":"SLC1A2 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 41","type":"exact"},{"name":"developmental and epileptic encephalopathy, 41","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in SLC1A2","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 41","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 41; EIEE41","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 41","type":"exact"}],"termid":"MONDO:0014916","xrefs":{"Monarch":{"xref_id":"0014916"}}}


id: PBO:0047403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 41","termid":"PBO:0047403"}


id: GO:0015149
data:
  {"annotated_genes":["SJAG_00057","SJAG_03820","SJAG_03608","SJAG_02719"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104887],"is_not":false,"summary":null,"term":"GO:0015149"},{"annotations":[66034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0055056"},{"annotations":[112604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005354"},{"annotations":[116155],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140108"},{"annotations":[119203],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005358"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a hexose sugar, a monosaccharide with 6 carbon atoms, from one side of a membrane to the other.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide transmembrane transporter activity","termid":"GO:0015145"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00057":null,"SJAG_02719":null,"SJAG_03608":null,"SJAG_03820":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"hexose transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5638222","Reactome:R-HSA-189242"],"termid":"GO:0015149","terms_by_termid":{"GO:0005354":null,"GO:0005358":null,"GO:0015149":null,"GO:0055056":null,"GO:0140108":null}}


id: MONDO:1010458
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypertrophic cardiomyopathy that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrophic cardiomyopathy, non-human animal","termid":"MONDO:1010015"},{"relation_name":"is_a","term_name":"cardiomyopathy, dog","termid":"MONDO:1010441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrophic cardiomyopathy, dog","secondary_identifiers":["OMIA:000515-9615"],"termid":"MONDO:1010458","xrefs":{"Monarch":{"xref_id":"1010458"}}}


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: SO:0005850
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Non-covalent primer binding site for initiation of replication, transcription, or reverse transcription.","direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide_binding_site","termid":"SO:0001655"},{"relation_name":"part_of","term_name":"LTR_retrotransposon","termid":"SO:0000186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primer_binding_site","secondary_identifiers":["http://en.wikipedia.org/wiki/Primer_binding_site"],"synonyms":[{"name":"INSDC_feature:primer_bind","type":"exact"},{"name":"primer binding site","type":"exact"}],"termid":"SO:0005850"}


id: GO:0007157
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of an adhesion molecule in one cell to a nonidentical adhesion molecule in an adjacent cell.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion via plasma-membrane adhesion molecules","termid":"GO:0098742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules","synonyms":[{"name":"agglutination","type":"related"}],"termid":"GO:0007157"}


id: GO:2000703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of fibroblast growth factor receptor signaling pathway involved in ureteric bud formation.","definition_xrefs":["GOC:yaf","GOC:obol","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of fibroblast growth factor receptor signaling pathway","termid":"GO:0040037"},{"relation_name":"is_a","term_name":"regulation of fibroblast growth factor receptor signaling pathway involved in ureteric bud formation","termid":"GO:2000702"},{"relation_name":"negatively_regulates","term_name":"fibroblast growth factor receptor signaling pathway involved in ureteric bud formation","termid":"GO:2000699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of fibroblast growth factor receptor signaling pathway involved in ureteric bud formation","synonyms":[{"name":"negative regulation of FGF receptor signaling pathway of ureteric bud formation","type":"exact"},{"name":"negative regulation of FGF receptor signalling pathway of ureteric bud formation","type":"exact"},{"name":"negative regulation of FGFR signaling pathway of ureteric bud formation","type":"exact"},{"name":"negative regulation of fibroblast growth factor receptor signaling pathway of ureteric bud formation","type":"exact"},{"name":"negative regulation of fibroblast growth factor receptor signalling pathway of ureteric bud formation","type":"exact"}],"termid":"GO:2000703"}


id: PBO:0040756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB","termid":"PBO:0040756"}


id: GO:1904865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of beta-catenin-TCF complex assembly.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:bf","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"regulation of beta-catenin-TCF complex assembly","termid":"GO:1904863"},{"relation_name":"positively_regulates","term_name":"beta-catenin-TCF complex assembly","termid":"GO:1904837"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"positive regulation of beta-catenin-TCF complex assembly","synonyms":[{"name":"activation of beta-catenin-TCF complex assembly","type":"narrow"},{"name":"activation of beta-catenin-TCF complex formation","type":"narrow"},{"name":"activation of beta-catenin/LEF complex assembly","type":"narrow"},{"name":"activation of beta-catenin/LEF complex formation","type":"narrow"},{"name":"activation of beta-catenin/T-cell factor complex assembly","type":"related"},{"name":"activation of beta-catenin/T-cell factor complex formation","type":"related"},{"name":"activation of beta-catenin/lymphoid enhancer binding factor complex assembly","type":"related"},{"name":"activation of beta-catenin/lymphoid enhancer binding factor complex formation","type":"related"},{"name":"positive regulation of beta-catenin-TCF complex formation","type":"exact"},{"name":"positive regulation of beta-catenin/LEF complex assembly","type":"narrow"},{"name":"positive regulation of beta-catenin/LEF complex formation","type":"narrow"},{"name":"positive regulation of beta-catenin/T-cell factor complex assembly","type":"related"},{"name":"positive regulation of beta-catenin/T-cell factor complex formation","type":"related"},{"name":"positive regulation of beta-catenin/lymphoid enhancer binding factor complex assembly","type":"related"},{"name":"positive regulation of beta-catenin/lymphoid enhancer binding factor complex formation","type":"related"},{"name":"up regulation of beta-catenin-TCF complex assembly","type":"exact"},{"name":"up regulation of beta-catenin-TCF complex formation","type":"exact"},{"name":"up regulation of beta-catenin/LEF complex assembly","type":"narrow"},{"name":"up regulation of beta-catenin/LEF complex formation","type":"narrow"},{"name":"up regulation of beta-catenin/T-cell factor complex assembly","type":"related"},{"name":"up regulation of beta-catenin/T-cell factor complex formation","type":"related"},{"name":"up regulation of beta-catenin/lymphoid enhancer binding factor complex assembly","type":"related"},{"name":"up regulation of beta-catenin/lymphoid enhancer binding factor complex formation","type":"related"},{"name":"up-regulation of beta-catenin-TCF complex assembly","type":"exact"},{"name":"up-regulation of beta-catenin-TCF complex formation","type":"exact"},{"name":"up-regulation of beta-catenin/LEF complex assembly","type":"narrow"},{"name":"up-regulation of beta-catenin/LEF complex formation","type":"narrow"},{"name":"up-regulation of beta-catenin/T-cell factor complex assembly","type":"related"},{"name":"up-regulation of beta-catenin/T-cell factor complex formation","type":"related"},{"name":"up-regulation of beta-catenin/lymphoid enhancer binding factor complex assembly","type":"related"},{"name":"up-regulation of beta-catenin/lymphoid enhancer binding factor complex formation","type":"related"},{"name":"upregulation of beta-catenin-TCF complex assembly","type":"exact"},{"name":"upregulation of beta-catenin-TCF complex formation","type":"exact"},{"name":"upregulation of beta-catenin/LEF complex assembly","type":"narrow"},{"name":"upregulation of beta-catenin/LEF complex formation","type":"narrow"},{"name":"upregulation of beta-catenin/T-cell factor complex assembly","type":"related"},{"name":"upregulation of beta-catenin/T-cell factor complex formation","type":"related"},{"name":"upregulation of beta-catenin/lymphoid enhancer binding factor complex assembly","type":"related"},{"name":"upregulation of beta-catenin/lymphoid enhancer binding factor complex formation","type":"related"}],"termid":"GO:1904865"}


id: GO:0015905
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of bicyclomycin across a lipid bilayer, from one side of a membrane to the other. Bicyclomycin (or bicozamycin) is an antibacterial drug often used as a livestock feed additive.","definition_xrefs":["PMID:20067529"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"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:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"bicyclomycin transmembrane transport","synonyms":[{"name":"bicyclomycin transport","type":"broad"}],"termid":"GO:0015905"}


id: GO:0099548
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell-cell signaling between presynapse and postsynapse mediated by nitric oxide.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synaptic signaling by nitric oxide","termid":"GO:0099163"},{"relation_name":"is_a","term_name":"trans-synaptic signaling by soluble gas","termid":"GO:0099543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"trans-synaptic signaling by nitric oxide","termid":"GO:0099548"}


id: GO:0009150
data:
  {"annotated_genes":["SJAG_00985","SJAG_01081","SJAG_02135","SJAG_02785","SJAG_00685","SJAG_MIT37","SJAG_00133","SJAG_02038","SJAG_02364","SJAG_04123","SJAG_01070","SJAG_00044","SJAG_04681","SJAG_00964","SJAG_02850","SJAG_00836","SJAG_04122","SJAG_02107","SJAG_04048","SJAG_07003","SJAG_01471","SJAG_03373","SJAG_02945","SJAG_06621","SJAG_00438","SJAG_MIT15","SJAG_04334","SJAG_06634","SJAG_04634","SJAG_04870","SJAG_02481","SJAG_04192","SJAG_03903","SJAG_02105","SJAG_02009","SJAG_02887","SJAG_03114","SJAG_01859","SJAG_01661","SJAG_03828","SJAG_04495","SJAG_00027","SJAG_03660","SJAG_04422","SJAG_06622","SJAG_00605","SJAG_MIT09","SJAG_00542","SJAG_02796","SJAG_05314","SJAG_02564","SJAG_00136","SJAG_04849","SJAG_02598","SJAG_03140","SJAG_01310","SJAG_00461","SJAG_02369","SJAG_03925","SJAG_05204","SJAG_00839","SJAG_01814","SJAG_01298","SJAG_03355","SJAG_00915"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78755,80749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044208"},{"annotations":[60474,65385,58242,66761,73342,78530,57101,71658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006189"},{"annotations":[81054],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901911"},{"annotations":[73651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006172"},{"annotations":[59742,78167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046033"},{"annotations":[57253,75696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044209"},{"annotations":[68947,59743,68867],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046034"},{"annotations":[118362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006198"},{"annotations":[107376,107746,74188,111346,100139,118333,99868,111341,111345,105284,107374,107745,79614,111340,111342,107375,96380,105543,111343,111344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"},{"annotations":[65313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046710"},{"annotations":[90422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061613"},{"annotations":[59761,63848],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006177"},{"annotations":[65312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046037"},{"annotations":[103087,77407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"},{"annotations":[104134,76666,65591],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006183"},{"annotations":[80750],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046040"},{"annotations":[65904,77408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032264"},{"annotations":[77909,74840],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045820"},{"annotations":[120000],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905707"},{"annotations":[121079,90951,106930,117828,121085,110734,103714,121073,109744,105581,95122,94695,96703,95713,104937,109836,105555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042776"},{"annotations":[71751],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006110"},{"annotations":[77409,110213],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving a purine ribonucleotide, a compound consisting of ribonucleoside (a purine base linked to a ribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide metabolic process","termid":"GO:0006163"},{"relation_name":"is_a","term_name":"ribonucleotide metabolic process","termid":"GO:0009259"}],"gene_count":65,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00044":null,"SJAG_00133":null,"SJAG_00136":null,"SJAG_00438":null,"SJAG_00461":null,"SJAG_00542":null,"SJAG_00605":null,"SJAG_00685":null,"SJAG_00836":null,"SJAG_00839":null,"SJAG_00915":null,"SJAG_00964":null,"SJAG_00985":null,"SJAG_01070":null,"SJAG_01081":null,"SJAG_01298":null,"SJAG_01310":null,"SJAG_01471":null,"SJAG_01661":null,"SJAG_01814":null,"SJAG_01859":null,"SJAG_02009":null,"SJAG_02038":null,"SJAG_02105":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02364":null,"SJAG_02369":null,"SJAG_02481":null,"SJAG_02564":null,"SJAG_02598":null,"SJAG_02785":null,"SJAG_02796":null,"SJAG_02850":null,"SJAG_02887":null,"SJAG_02945":null,"SJAG_03114":null,"SJAG_03140":null,"SJAG_03355":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_03925":null,"SJAG_04048":null,"SJAG_04122":null,"SJAG_04123":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04422":null,"SJAG_04495":null,"SJAG_04634":null,"SJAG_04681":null,"SJAG_04849":null,"SJAG_04870":null,"SJAG_05204":null,"SJAG_05314":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06634":null,"SJAG_07003":null,"SJAG_MIT09":null,"SJAG_MIT15":null,"SJAG_MIT37":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"purine ribonucleotide metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"purine ribonucleotide metabolism","type":"exact"}],"termid":"GO:0009150","terms_by_termid":{"GO:0006110":null,"GO:0006172":null,"GO:0006177":null,"GO:0006183":null,"GO:0006189":null,"GO:0006198":null,"GO:0032263":null,"GO:0032264":null,"GO:0032265":null,"GO:0042776":null,"GO:0044208":null,"GO:0044209":null,"GO:0045820":null,"GO:0046033":null,"GO:0046034":null,"GO:0046037":null,"GO:0046040":null,"GO:0046710":null,"GO:0061613":null,"GO:0061621":null,"GO:1901911":null,"GO:1905707":null}}


id: GO:0002017
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the hormone aldosterone decreases the rate of diuresis and natriuresis resulting in increased blood volume.","definition_xrefs":["GOC:dph","GOC:tb","ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal system process involved in regulation of blood volume","termid":"GO:0001977"},{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure by hormone","termid":"GO:0001990"},{"relation_name":"is_a","term_name":"positive regulation of systemic arterial blood pressure","termid":"GO:0003084"}],"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 blood volume by renal aldosterone","synonyms":[{"name":"aldosterone mediated control of body fluids","type":"related"},{"name":"aldosterone mediated regulation of blood volume","type":"exact"},{"name":"renal regulation of blood volume by aldosterone","type":"exact"}],"termid":"GO:0002017"}


id: PBO:0006187
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_upstream_target","termid":"PBO:0006187"}


id: MONDO:1010616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital hypothyroidism in dogs in which the cause of the disease is a mutation in the SCL5AG gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypothyroidism, dog","termid":"MONDO:1010602"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital dyshormonogenic hypothyroidism with goiter, SLC5A5-related, dog","secondary_identifiers":["OMIA:002174-9615"],"termid":"MONDO:1010616","xrefs":{"Monarch":{"xref_id":"1010616"}}}


id: MONDO:0100271
data:
  {"annotated_genes":["SJAG_05950"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013938"},{"annotations":[89038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013939"}]},"cv_name":"mondo","definition":"Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX26 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Zellweger spectrum disorders","termid":"MONDO:0019609"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019053"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0005244","MONDO:0006025","MONDO:0019053"],"is_obsolete":false,"name":"peroxisome biogenesis disorder due to PEX26 defect","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"PEX26 related Zellweger spectrum disorder","type":"exact"},{"name":"peroxisome biogenesis disorder due to PEX26 defect","type":"exact"}],"termid":"MONDO:0100271","terms_by_termid":{"MONDO:0013938":null,"MONDO:0013939":null},"xrefs":{"Monarch":{"xref_id":"0100271"}}}


id: PBO:0065074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRICKLE2 antisense RNA 3","termid":"PBO:0065074"}


id: GO:0021743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the hypoglossal nucleus over time, from its formation to the mature structure.","definition_xrefs":["GOC:dph","GOC:cls","GOC:jid","GO_REF:0000021","GOC:dgh","GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"medulla oblongata development","termid":"GO:0021550"}],"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":"hypoglossal nucleus development","termid":"GO:0021743"}


id: PR:O74745
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- anp1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74745"],"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":"mannan polymerase II complex anp1 subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1734.04","synonyms":[{"name":"M-Pol II subunit anp1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-anp1","type":"exact"}],"termid":"PR:O74745"}


id: MONDO:0035785
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-syndromic anorectal malformation with vestibular fistula (obsolete MONDO:0035785)","secondary_identifiers":["Orphanet:600993"],"termid":"MONDO:0035785","xrefs":{"Monarch":{"xref_id":"0035785"}}}


id: PBO:0048478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosaminyl (N-acetyl) transferase 1 pseudogene 5","termid":"PBO:0048478"}


id: GO:0070468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release by odontoblasts of the extracellular matrix constituents, including collagen, that form the basis of dentin.","definition_xrefs":["PMID:12856968","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix constituent secretion","termid":"GO:0070278"},{"relation_name":"part_of","term_name":"odontogenesis of dentin-containing tooth","termid":"GO:0042475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"dentin extracellular matrix secretion","synonyms":[{"name":"dentin secretion","type":"related"},{"name":"dentine secretion","type":"related"},{"name":"predentin secretion","type":"related"}],"termid":"GO:0070468"}


id: GO:0015438
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + teichoic acid(in) = ADP + phosphate + teichoic acid(out).","definition_xrefs":["PMID:7565096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule transmembrane transporter activity","termid":"GO:0022884"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"},{"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:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ABC-type teichoic acid transporter activity","secondary_identifiers":["EC:7.5.2.4","GO:0015162","MetaCyc:3.6.3.40-RXN"],"synonyms":[{"name":"ABC-type teichoic-acid transporter","type":"exact"},{"name":"ATP-dependent teichoic acid transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled teichoic acid transmembrane transporter activity","type":"related"},{"name":"teichoic acid transmembrane transporter activity","type":"broad"},{"name":"teichoic-acid ABC transporter","type":"exact"},{"name":"teichoic-acid-transporting ATPase activity","type":"related"}],"termid":"GO:0015438"}


id: PBO:0109016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family member 17, pseudogene","termid":"PBO:0109016"}


id: MONDO:0030312
data:
  {"annotated_genes":["SJAG_00380"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88378],"is_not":false,"summary":null,"term":"MONDO:0030312"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00380":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"spinocerebellar ataxia, autosomal recessive 29","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619389","DOID:0070410","MEDGEN:1788435","UMLS:C5543595"],"synonyms":[{"name":"Barakat-Van Ham-Kaya syndrome","type":"exact"},{"name":"SCAR29","type":"exact"},{"name":"neurodevelopmental disorder with hypotonia and cerebellar ataxia","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 29","type":"exact"}],"termid":"MONDO:0030312","terms_by_termid":{"MONDO:0030312":null},"xrefs":{"Monarch":{"xref_id":"0030312"}}}


id: GO:0030246
data:
  {"annotated_genes":["SJAG_01991","SJAG_00530","SJAG_01858","SJAG_03824","SJAG_02839","SJAG_00839","SJAG_02131","SJAG_00667","SJAG_00981","SJAG_03818","SJAG_03280","SJAG_04495","SJAG_02951","SJAG_04334","SJAG_03535","SJAG_04571"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57957,58081,60831,66405,69695,69727,95389],"is_not":false,"summary":null,"term":"GO:0030246"},{"annotations":[61232],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030248"},{"annotations":[57552,65537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005536"},{"annotations":[112705,81022,115740,120529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005537"},{"annotations":[120532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001065"},{"annotations":[71947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048029"},{"annotations":[102041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030247"}]},"cv_name":"molecular_function","definition":"Binding to a carbohydrate, which includes monosaccharides, oligosaccharides and polysaccharides as well as substances derived from monosaccharides by reduction of the carbonyl group (alditols), by oxidation of one or more hydroxy groups to afford the corresponding aldehydes, ketones, or carboxylic acids, or by replacement of one or more hydroxy group(s) by a hydrogen atom. Cyclitols are generally not regarded as carbohydrates.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00530":null,"SJAG_00667":null,"SJAG_00839":null,"SJAG_00981":null,"SJAG_01858":null,"SJAG_01991":null,"SJAG_02131":null,"SJAG_02839":null,"SJAG_02951":null,"SJAG_03280":null,"SJAG_03535":null,"SJAG_03818":null,"SJAG_03824":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_04571":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"carbohydrate binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0005529"],"synonyms":[{"name":"selectin","type":"related"},{"name":"sugar binding","type":"exact"}],"termid":"GO:0030246","terms_by_termid":{"GO:0005536":null,"GO:0005537":null,"GO:0030246":null,"GO:0030247":null,"GO:0030248":null,"GO:0048029":null,"GO:2001065":null}}


id: PBO:0068821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 59, pseudogene","termid":"PBO:0068821"}


id: PBO:0035925
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H3-K9_dimethylation_at_centromere_inner_repeat_during_vegetative_growth","termid":"PBO:0035925"}


id: PBO:0081723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF652 antisense RNA 1","termid":"PBO:0081723"}


id: MONDO:0023726
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extragonadal non-seminomatous malignant germ cell tumor that arises from the mediastinum. It is characterized by the presence of small pale cells with small amount of cytoplasm and round to oval nuclei with small nucleoli forming a variety of patterns, including microcystic, macrocystic, pseudopapillary, myxomatous, hepatoid, polyvesicular vitelline, and solid. It manifests with respiratory distress, thoracic pain, fever, and superior vena cava syndrome.","definition_xrefs":["NCIT:C6443"],"direct_ancestors":[{"relation_name":"is_a","term_name":"yolk sac tumor","termid":"MONDO:0005744"},{"relation_name":"is_a","term_name":"mediastinal malignant germ cell tumor","termid":"MONDO:0006298"}],"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":"mediastinal yolk sac tumor","secondary_identifiers":["MEDGEN:233176","UMLS:C1334683"],"synonyms":[{"name":"EST","type":"related"},{"name":"endodermal sinus neoplasm of mediastinum","type":"exact"},{"name":"endodermal sinus neoplasm of the mediastinum","type":"exact"},{"name":"endodermal sinus tumor of mediastinum","type":"exact"},{"name":"endodermal sinus tumor of the mediastinum","type":"exact"},{"name":"endodermal sinus tumour of mediastinum","type":"exact"},{"name":"endodermal sinus tumour of the mediastinum","type":"exact"},{"name":"mediastinal endodermal sinus neoplasm","type":"exact"},{"name":"mediastinal endodermal sinus tumor","type":"exact"},{"name":"mediastinal endodermal sinus tumors","type":"related"},{"name":"mediastinal endodermal sinus tumour","type":"exact"},{"name":"mediastinal endodermal sinus tumours","type":"related"},{"name":"mediastinal yolk Sac neoplasm","type":"exact"},{"name":"mediastinal yolk Sac tumor","type":"exact"},{"name":"mediastinal yolk Sac tumour","type":"exact"},{"name":"mediastinum yolk sac tumor","type":"exact"},{"name":"mediastinum yolk sac tumour","type":"exact"},{"name":"yolk Sac neoplasm of mediastinum","type":"exact"},{"name":"yolk Sac neoplasm of the mediastinum","type":"exact"},{"name":"yolk Sac tumor of mediastinum","type":"exact"},{"name":"yolk Sac tumor of the mediastinum","type":"exact"},{"name":"yolk Sac tumour of mediastinum","type":"exact"},{"name":"yolk Sac tumour of the mediastinum","type":"exact"}],"termid":"MONDO:0023726","xrefs":{"Monarch":{"xref_id":"0023726"}}}


id: MONDO:0042913
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schrander-stumpel-Theunissen-Hulsmans syndrome","secondary_identifiers":["MESH:C536639","UMLS:C2931275","MEDGEN:419033"],"synonyms":[{"name":"Schrander-Stumpel Theunissen Hulsmans syndrome","type":"related"},{"name":"vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism","type":"related"},{"name":"vitiligo, psychomotor retardation, cleft palate and facial dysmorphism","type":"related"}],"termid":"MONDO:0042913","xrefs":{"Monarch":{"xref_id":"0042913"}}}


id: PBO:0076576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 3 pseudogene 4","termid":"PBO:0076576"}


id: MONDO:0013718
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the WDR19 gene on chromosome 4p14.","definition_xrefs":["DOID:0111121","PMID:22019273"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephronophthisis","termid":"MONDO:0019005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0006025"],"is_obsolete":false,"name":"nephronophthisis 13","secondary_identifiers":["OMIM:614377","UMLS:C3280612","MEDGEN:482242"],"synonyms":[{"name":"NPHP13","type":"exact"},{"name":"nephronophthisis 13","type":"exact"},{"name":"nephronophthisis type 13","type":"exact"}],"termid":"MONDO:0013718","xrefs":{"Monarch":{"xref_id":"0013718"}}}


id: MONDO:0007976
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":"mesomelic dwarfism of hypoplastic tibia and radius type","secondary_identifiers":["UMLS:C1835010","MESH:C563589","MEDGEN:322550","OMIM:156230"],"synonyms":[{"name":"mesomelic dwarfism of hypoplastic tibia and radius type","type":"exact"}],"termid":"MONDO:0007976","xrefs":{"Monarch":{"xref_id":"0007976"}}}


id: MONDO:0023670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Bardet-Biedl syndrome","termid":"MONDO:0015229"}],"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":"Bardet-Biedl syndrome 20","secondary_identifiers":["OMIM:619471","UMLS:C4310707","DOID:0081009","MEDGEN:934674"],"synonyms":[{"name":"BBS20","type":"exact"}],"termid":"MONDO:0023670","xrefs":{"Monarch":{"xref_id":"0023670"}}}


id: PBO:0066781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 79","termid":"PBO:0066781"}


id: GO:0150195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of substances (e.g. macromolecules, small molecules, ions) through the blood-cerebrospinal fluid barrier.","definition_xrefs":["PMID:21349151","GOC:bc","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular transport","termid":"GO:0010232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"transport across blood-cerebrospinal fluid barrier","synonyms":[{"name":"transport across BCSFB","type":"exact"},{"name":"transport across blood-CSF barrier","type":"exact"},{"name":"transport across blood/CSF barrier","type":"exact"},{"name":"transport across blood/cerebrospinal fluid barrier","type":"exact"}],"termid":"GO:0150195"}


id: GO:0044547
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a DNA topoisomerase.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"DNA topoisomerase binding","secondary_identifiers":["GO:0017033"],"synonyms":[{"name":"DNA topoisomerase I binding","type":"narrow"}],"termid":"GO:0044547"}


id: PBO:0065673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTPRT antisense RNA 1","termid":"PBO:0065673"}


id: MONDO:1012435
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hydranencephaly and cerebellar hypoplasia, non-human animal","termid":"MONDO:1011888"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital hydranencephaly and cerebellar hypoplasia, cattle","secondary_identifiers":["OMIA:001689-9913"],"termid":"MONDO:1012435","xrefs":{"Monarch":{"xref_id":"1012435"}}}


id: PBO:0071048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 50","termid":"PBO:0071048"}


id: FYPO:0000228
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 sister chromatids do not move towards the spindle poles at the same time during mitosis, but instead one or more chromosomes remain distant from the spindle pole after the bulk of the DNA has separated. Mitotic sister chromatid segregation may stop before completing separation of chromosomes, or may eventually be completed.","definition_xrefs":["PMID:20211136","PMID:11809834","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"is_a","term_name":"lagging chromosomes","termid":"FYPO:0002090"}],"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:0000337"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000641","FYPO:0001320","FYPO:0000002","FYPO:0000631","FYPO:0000337"],"is_obsolete":false,"name":"lagging mitotic chromosomes","synonyms":[{"name":"chromosome segregation defects, lagging mitotic chromosomes","type":"exact"},{"name":"lagging chromosomes during mitotic cell cycle","type":"related"},{"name":"lagging chromosomes during vegetative growth","type":"exact"},{"name":"lagging mitotic sister chromatids","type":"exact"}],"termid":"FYPO:0000228"}


id: PBO:0005875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"15S rRNA","termid":"PBO:0005875"}


id: PBO:0065092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase AMP-activated non-catalytic subunit gamma 1","termid":"PBO:0065092"}


id: PBO:0089537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H2B-K119 ubiquitin ligase complex (HULC) subunit, ubiquitin-protein ligase E3 Brl2","termid":"PBO:0089537"}


id: GO:0102202
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + solasodine = UDP + solasodine 3-O-beta-D-glucopyranoside + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete soladodine glucosyltransferase activity (obsolete GO:0102202)","termid":"GO:0102202"}


id: GO:0005599
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(X) chains; type X collagen triple helices form hexagonal networks (sheets).","definition_xrefs":["PMID:21421911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"network-forming collagen trimer","termid":"GO:0098642"},{"relation_name":"part_of","term_name":"interstitial hexagonal collagen network","termid":"GO:0098646"}],"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":"collagen type X trimer","termid":"GO:0005599"}


id: GO:1903305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of regulated secretory pathway.","definition_xrefs":["PMID:12526776","GO_REF:0000058","GOC:pad","GOC:TermGenie","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of exocytosis","termid":"GO:0017157"},{"relation_name":"regulates","term_name":"regulated exocytosis","termid":"GO:0045055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"regulation of regulated secretory pathway","termid":"GO:1903305"}


id: GO:0071900
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of protein serine/threonine kinase activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein kinase activity","termid":"GO:0045859"}],"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 protein serine/threonine kinase activity","termid":"GO:0071900"}


id: MONDO:0859189
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":"muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome","secondary_identifiers":["OMIM:619518","UMLS:C5561980","MEDGEN:1794190"],"termid":"MONDO:0859189","xrefs":{"Monarch":{"xref_id":"0859189"}}}


id: MONDO:1010056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypoparathyroidism that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoparathyroidism, non-human animal","secondary_identifiers":["OMIA:000528"],"termid":"MONDO:1010056","xrefs":{"Monarch":{"xref_id":"1010056"}}}


id: PBO:0066831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 130","termid":"PBO:0066831"}


id: PBO:0059584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylthioadenosine phosphorylase pseudogene 1","termid":"PBO:0059584"}


id: MONDO:1010964
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lymphangiosarcoma that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"canine sarcoma","termid":"MONDO:0700149"},{"relation_name":"is_a","term_name":"lymphangiosarcoma, non-human animal","termid":"MONDO:1010226"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lymphangiosarcoma, dog","secondary_identifiers":["OMIA:002476-9615"],"termid":"MONDO:1010964","xrefs":{"Monarch":{"xref_id":"1010964"}}}


id: GO:2000725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac muscle cell differentiation.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of striated muscle cell differentiation","termid":"GO:0051153"},{"relation_name":"is_a","term_name":"regulation of cardiocyte differentiation","termid":"GO:1905207"},{"relation_name":"regulates","term_name":"cardiac muscle cell differentiation","termid":"GO:0055007"}],"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 cardiac muscle cell differentiation","synonyms":[{"name":"regulation of cardiomyocyte differentiation","type":"exact"},{"name":"regulation of heart muscle cell differentiation","type":"related"}],"termid":"GO:2000725"}


id: PBO:0074984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 114-26","termid":"PBO:0074984"}


id: GO:0102619
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oryzalexin A + NAD(P) = oryzalexin C + H+ + NAD(P)H.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oryzalexin C synthase (oryzalexin A dependent) activity (obsolete GO:0102619)","termid":"GO:0102619"}


id: MONDO:0009342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare malformative association, described in only two siblings to date, and characterized by Hirschsprung disease (defined by the presence of an aganglionic segment of variable extent in the terminal part of the colon that leads to the symptoms of intestinal obstruction including constipation and abdominal distension), polydactyly of hands and/or feet, unilateral renal agenesis, hypertelorism and congenital deafness. There have been no further descriptions in the literature since 1988.","definition_xrefs":["Orphanet:2155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"intestinal motility disease","termid":"MONDO:0021189"}],"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":"Hirschsprung disease-hearing loss-polydactyly syndrome","secondary_identifiers":["GARD:157","MEDGEN:341066","MESH:C565518","OMIM:235740","UMLS:C1856112","SCTID:721221000"],"synonyms":[{"name":"Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness","type":"narrow"},{"name":"Hirschsprung disease with polydactyly, renal agenesis, and deafness","type":"narrow"},{"name":"Hirschsprung disease, deafness and polydactyly","type":"narrow"},{"name":"Hirschsprung disease-deafness-polydactyly syndrome","type":"narrow"},{"name":"Santos Mateus Leal syndrome","type":"related"},{"name":"Santos-Mateus-Leal syndrome","type":"exact"}],"termid":"MONDO:0009342","xrefs":{"Monarch":{"xref_id":"0009342"}}}


id: MONDO:0043187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pulmonary artery agenesis (obsolete MONDO:0043187)","termid":"MONDO:0043187","xrefs":{"Monarch":{"xref_id":"0043187"}}}


id: PBO:0091647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane amino acid transmembrane transporter Aat1","termid":"PBO:0091647"}


id: PBO:0001995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannosyl-oligosaccharide 1,2-alpha-mannosidase","termid":"PBO:0001995"}


id: PATO:0000092
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000092 abiotic stress sensitivity (obsolete PATO:0000092)","termid":"PATO:0000092"}


id: GO:0034611
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the exonucleolytic cleavage of oligoribonucleotides to yield ribonucleoside 5'-phosphates.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete oligoribonucleotidase activity (obsolete GO:0034611)","secondary_identifiers":["Reactome:R-HSA-9009950","Reactome:R-HSA-9615042"],"synonyms":[{"name":"RNA oligonucleotidase activity","type":"exact"}],"termid":"GO:0034611"}


id: PATO:0000375
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A distance which is lesser relative to the normal or average.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"distance","termid":"PATO:0000040"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased distance","synonyms":[{"name":"short distance","type":"related"}],"termid":"PATO:0000375"}


id: GO:0098752
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the plasma membrane consisting of the gene products that penetrate only the cytoplasmic side of the membrane.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of the cytoplasmic side of the plasma membrane (obsolete GO:0098752)","termid":"GO:0098752"}


id: MONDO:0026192
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic glomerular disease (obsolete MONDO:0026192)","secondary_identifiers":["Orphanet:183586"],"termid":"MONDO:0026192","xrefs":{"Monarch":{"xref_id":"0026192"}}}


id: GO:0070350
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of white fat cell proliferation.","definition_xrefs":["GOC:mah","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of fat cell proliferation","termid":"GO:0070344"},{"relation_name":"regulates","term_name":"white fat cell proliferation","termid":"GO:0070343"}],"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 white fat cell proliferation","synonyms":[{"name":"regulation of white adipocyte proliferation","type":"exact"},{"name":"regulation of white adipose cell proliferation","type":"exact"}],"termid":"GO:0070350"}


id: PBO:0064114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polycystin 1, transient receptor potential channel interacting pseudogene 1","termid":"PBO:0064114"}


id: MONDO:0045003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease or disorder that involves the scrotum.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scrotal disorder","secondary_identifiers":["UMLS:C0268919","SCTID:49701002","MEDGEN:541586"],"synonyms":[{"name":"disease of scrotum","type":"exact"},{"name":"disease or disorder of scrotum","type":"exact"},{"name":"disorder of scrotum","type":"exact"},{"name":"scrotum disease","type":"exact"},{"name":"scrotum disease or disorder","type":"exact"}],"termid":"MONDO:0045003","xrefs":{"Monarch":{"xref_id":"0045003"}}}


id: PBO:0063004
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"platelet activating factor acetylhydrolase 1b regulatory subunit 1 pseudogene 1","termid":"PBO:0063004"}


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


id: PBO:0080414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar protein sorting 45 homolog","termid":"PBO:0080414"}


id: PBO:0048149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FYN binding protein 1","termid":"PBO:0048149"}


id: GO:1900703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of orcinol biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"is_a","term_name":"regulation of orcinol biosynthetic process","termid":"GO:1900701"},{"relation_name":"positively_regulates","term_name":"orcinol biosynthetic process","termid":"GO:0046197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"positive regulation of orcinol biosynthetic process","synonyms":[{"name":"activation of orcinol anabolism","type":"exact"},{"name":"activation of orcinol biosynthesis","type":"exact"},{"name":"activation of orcinol biosynthetic process","type":"narrow"},{"name":"activation of orcinol formation","type":"exact"},{"name":"activation of orcinol synthesis","type":"exact"},{"name":"positive regulation of orcinol anabolism","type":"exact"},{"name":"positive regulation of orcinol biosynthesis","type":"exact"},{"name":"positive regulation of orcinol formation","type":"exact"},{"name":"positive regulation of orcinol synthesis","type":"exact"},{"name":"up regulation of orcinol anabolism","type":"exact"},{"name":"up regulation of orcinol biosynthesis","type":"exact"},{"name":"up regulation of orcinol biosynthetic process","type":"exact"},{"name":"up regulation of orcinol formation","type":"exact"},{"name":"up regulation of orcinol synthesis","type":"exact"},{"name":"up-regulation of orcinol anabolism","type":"exact"},{"name":"up-regulation of orcinol biosynthesis","type":"exact"},{"name":"up-regulation of orcinol biosynthetic process","type":"exact"},{"name":"up-regulation of orcinol formation","type":"exact"},{"name":"up-regulation of orcinol synthesis","type":"exact"},{"name":"upregulation of orcinol anabolism","type":"exact"},{"name":"upregulation of orcinol biosynthesis","type":"exact"},{"name":"upregulation of orcinol biosynthetic process","type":"exact"},{"name":"upregulation of orcinol formation","type":"exact"},{"name":"upregulation of orcinol synthesis","type":"exact"}],"termid":"GO:1900703"}


id: PBO:0082473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calpain-like cysteine protease; involved in proteolytic activation of Rim101p in response to alkaline pH; localizes to punctate structures in alkaline conditions and in vps4 mutant; has similarity to A. nidulans palB","termid":"PBO:0082473"}


id: FYPO:0001183
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of an alpha-glucosidase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000654","FYPO:0000652","FYPO:0001985","FYPO:0000661"],"is_obsolete":false,"name":"abnormal alpha-glucosidase activity","termid":"FYPO:0001183"}


id: PBO:0046322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enolase 1 pseudogene 3","termid":"PBO:0046322"}


id: MONDO:0000946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Involuntary spasm of the outer muscles of the vagina during penetration that results from a psychological cause.","definition_xrefs":["NCIT:C35113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"psychosexual disorder","termid":"MONDO:0000947"},{"relation_name":"is_a","term_name":"vaginismus","termid":"MONDO:0021723"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psychologic vaginismus","secondary_identifiers":["DOID:10131","MEDGEN:52970","SCTID:71787009","UMLS:C0042266","ICD9:306.51"],"synonyms":[{"name":"functional vaginismus","type":"exact"},{"name":"non-organic vaginismus","type":"exact"},{"name":"psychogenic vaginismus","type":"exact"}],"termid":"MONDO:0000946","xrefs":{"Monarch":{"xref_id":"0000946"}}}


id: GO:0009937
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of gibberellic acid mediated signaling.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"gibberellic acid mediated signaling pathway","termid":"GO:0009740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of gibberellic acid mediated signaling pathway","synonyms":[{"name":"regulation of gibberellic acid mediated signalling","type":"exact"}],"termid":"GO:0009937"}


id: PBO:0001215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-A chaperone Scm3","termid":"PBO:0001215"}


id: PBO:0088441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichyl-phosphate beta-glucosyltransferase Alg5","termid":"PBO:0088441"}


id: FYPO:0004480
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 from a calcineurin-dependent response element (CDRE)-containing promoter is decreased during a cellular response to micafungin.","definition_xrefs":["PMID:16928959","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased transcription from RNA polymerase II promoter during vegetative growth","termid":"FYPO:0005229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000294","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"decreased transcription from CDRE promoter in response to micafungin","synonyms":[{"name":"decreased transcription from CDRE promoter during cellular response to micafungin","type":"exact"},{"name":"decreased transcription from CDRE promoter in response to micafungin during mitotic cell cycle","type":"related"},{"name":"decreased transcription from CDRE promoter in response to micafungin during vegetative growth","type":"exact"},{"name":"reduced transcription from CDRE promoter in response to micafungin","type":"exact"}],"termid":"FYPO:0004480"}


id: PBQ:0000003
data:
  {"annotation_feature_type":"gene","cv_name":"pb_quiescence","definition":"Cell quiescence, i.e. a specialized resting state in which the cells do not grow or divide, and the gene expression pattern changes globally, that a cell enters following cell cycle arrest in G1 due to nitrogen limitation. In some cell types or under certain conditions, cellular metabolism may proceed.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell quiescence following G1 arrest","termid":"PBQ:0000002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell quiescence following G1 arrest due to nitrogen limitation","synonyms":[{"name":"cellular quiescence following G1 arrest due to nitrogen limitation","type":"exact"},{"name":"quiescence following G1 arrest due to nitrogen limitation","type":"broad"}],"termid":"PBQ:0000003"}


id: PBO:0042289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD2 cytoplasmic tail binding protein 2","termid":"PBO:0042289"}


id: PBO:0035812
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_H2A_phosphorylation_at_tRNA_genes_during_vegetative_growth","termid":"PBO:0035812"}


id: MONDO:0015917
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete malignant glioma (obsolete MONDO:0015917)","termid":"MONDO:0015917","xrefs":{"Monarch":{"xref_id":"0015917"}}}


id: MONDO:0011589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, isolated, with coloboma","termid":"MONDO:0000170"}],"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":"microphthalmia with coloboma 2","secondary_identifiers":["MEDGEN:343030","UMLS:C1854018","OMIM:605738","MESH:C565300","GARD:15385"],"synonyms":[{"name":"MCOPCB2","type":"exact"},{"name":"microphthalmia, colobomatous, isolated 2","type":"related"},{"name":"microphthalmia, isolated, with coloboma 2","type":"related"}],"termid":"MONDO:0011589","xrefs":{"Monarch":{"xref_id":"0011589"}}}


id: FYPO:0003737
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, begins later than normal during G2 phase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"delayed onset of protein phosphorylation during vegetative growth","termid":"FYPO:0002830"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0002494","FYPO:0002274"],"is_obsolete":false,"name":"delayed onset of protein phosphorylation during mitotic G2 phase","synonyms":[{"name":"delayed onset of protein phosphorylation during mitotic G2 phase during vegetative growth","type":"exact"},{"name":"delayed onset of protein phosphorylation during mitotic G2-phase","type":"exact"},{"name":"delayed onset of protein/peptide phosphorylation during mitotic G2 phase","type":"exact"},{"name":"delayed protein phosphorylation during mitotic G2 phase","type":"exact"}],"termid":"FYPO:0003737"}


id: FYPO:0002330
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 4 of histone H3 is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone methylation during vegetative growth","termid":"FYPO:0000457"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0002494","FYPO:0000002"],"is_obsolete":false,"name":"abnormal histone H3-K4 methylation during vegetative growth","synonyms":[{"name":"abnormal histone H3 K4 methylation during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K4 methylation during mitotic cell cycle","type":"related"},{"name":"abnormal histone H3K4me during vegetative growth","type":"exact"},{"name":"abnormal histone lysine H3 K4 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002330"}


id: MONDO:0005896
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with viruses of the family paramyxoviridae. This includes morbillivirus infections; respirovirus infections; pneumovirus infections; henipavirus infections; avulavirus infections; and rubulavirus infections.","definition_xrefs":["MESH:D018184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Mononegavirales infectious disease","termid":"MONDO:0005856"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Paramyxoviridae infectious disease","secondary_identifiers":["EFO:0007419"],"synonyms":[{"name":"Paramyxoviridae caused disease or disorder","type":"exact"},{"name":"Paramyxoviridae disease or disorder","type":"exact"}],"termid":"MONDO:0005896","xrefs":{"Monarch":{"xref_id":"0005896"}}}


id: PBO:0003430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically upregulated gene Mug97","termid":"PBO:0003430"}


id: PBO:0109407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA U2 snRNA-specific guide RNA","termid":"PBO:0109407"}


id: PBO:0059890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND1 pseudogene 13","termid":"PBO:0059890"}


id: PR:Q9P768
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A B(0,+)-type amino acid transporter 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01564"],"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 amino-acid permease P7G5.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP7G5.06","secondary_identifiers":["UniProtKB:Q9P768"],"synonyms":[{"name":"Spom972h-SLC7A9","type":"exact"}],"termid":"PR:Q9P768"}


id: MONDO:0003254
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare granular cell tumor that arises from the heart.","definition_xrefs":["NCIT:C5360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign granular cell tumor","termid":"MONDO:0003250"},{"relation_name":"is_a","term_name":"benign neoplasm of epicardium","termid":"MONDO:0021508"}],"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":"cardiac granular cell neoplasm","secondary_identifiers":["MEDGEN:232023","UMLS:C1332845","DOID:5044"],"synonyms":[{"name":"Cardiac granular cell neoplasm","type":"exact"},{"name":"Cardiac granular cell tumor","type":"exact"},{"name":"Cardiac granular cell tumour","type":"exact"},{"name":"granular cell neoplasm of heart","type":"exact"},{"name":"granular cell neoplasm of the heart","type":"exact"},{"name":"granular cell tumor of heart","type":"exact"},{"name":"granular cell tumor of the heart","type":"exact"},{"name":"granular cell tumour of heart","type":"exact"},{"name":"granular cell tumour of the heart","type":"exact"},{"name":"heart granular cell tumor","type":"exact"},{"name":"heart granular cell tumour","type":"exact"}],"termid":"MONDO:0003254","xrefs":{"Monarch":{"xref_id":"0003254"}}}


id: PBO:0090997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome assembly protein Rsa3","termid":"PBO:0090997"}


id: GO:0046189
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a phenol, any compound containing one or more hydroxyl groups directly attached to an aromatic carbon ring.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"}],"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":"phenol-containing compound biosynthetic process","synonyms":[{"name":"phenol-containing compound anabolism","type":"exact"},{"name":"phenol-containing compound biosynthesis","type":"exact"},{"name":"phenol-containing compound formation","type":"exact"},{"name":"phenol-containing compound synthesis","type":"exact"}],"termid":"GO:0046189"}


id: PR:Q9UT09
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAP8A3.07c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UT09"],"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":"phospho-2-dehydro-3-deoxyheptonate aldolase, tyrosine-inhibited (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP8A3.07c","synonyms":[{"name":"3-deoxy-D-arabino-heptulosonate 7-phosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DAHP synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPAP8A3.07c","type":"exact"},{"name":"phospho-2-keto-3-deoxyheptonate aldolase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT09"}


id: GO:0034733
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transcription factor TFIIIB-beta complex that contains the TATA-binding protein (TBP), B'' and BRF, and is involved in the regulation of transcription from type 2 RNA polymerase III promoters.","definition_xrefs":["PMID:11433012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription factor TFIIIB complex","termid":"GO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"transcription factor TFIIIB-beta complex","termid":"GO:0034733"}


id: PR:Q9URX3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A D-cysteine desulfhydrase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02270","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":"1-aminocyclopropane-1-carboxylate deaminase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC922.03","secondary_identifiers":["UniProtKB:Q9URX3"],"synonyms":[{"name":"ACC deaminase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ACCD (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-dcyD","type":"exact"}],"termid":"PR:Q9URX3"}


id: PBO:0042627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromodomain Y-linked 2B","termid":"PBO:0042627"}


id: FYPO:0000530
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the mitotic cell cycle arrest that normally occurs in response to pheromone is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of mitotic cell cycle","termid":"FYPO:0000148"},{"relation_name":"is_a","term_name":"abnormal response to pheromone","termid":"FYPO:0000302"},{"relation_name":"is_a","term_name":"abnormal occurrence of normal mitotic cell cycle arrest","termid":"FYPO:0001026"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001985","FYPO:0001320","FYPO:0000298","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal mitotic cell cycle arrest in response to pheromone","synonyms":[{"name":"abnormal pheromone-induced mitotic cell cycle arrest","type":"exact"},{"name":"pheromone-induced cell cycle arrest: abnormal","type":"related"}],"termid":"FYPO:0000530"}


id: PBO:0091540
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-terminal acetylation increases F-actin binding affinity","termid":"PBO:0091540"}


id: PBO:0052767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 59","termid":"PBO:0052767"}


id: MONDO:0011290
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":"dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability","secondary_identifiers":["OMIM:603133","UMLS:C1864183","MEDGEN:350359","MESH:C566408"],"synonyms":[{"name":"dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability","type":"exact"},{"name":"dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation","type":"exact"}],"termid":"MONDO:0011290","xrefs":{"Monarch":{"xref_id":"0011290"}}}


id: MONDO:0004406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mixed germ cell tumor of central nervous system that occurs in an adult.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult central nervous system germ cell tumor","termid":"MONDO:0003405"},{"relation_name":"is_a","term_name":"mixed germ cell tumor of central nervous system","termid":"MONDO:0016742"}],"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":"adult central nervous system mixed germ cell tumor","secondary_identifiers":["UMLS:C1332195","NCIT:C27402","DOID:7945","MEDGEN:231038"],"synonyms":[{"name":"adult central nervous system mixed germ cell tumor","type":"exact"},{"name":"adult mixed germ cell tumor of central nervous system","type":"exact"},{"name":"adult mixed germ cell tumour of central nervous system","type":"exact"},{"name":"central nervous system Mixed germ cell tumor","type":"broad"},{"name":"central nervous system Mixed germ cell tumour","type":"broad"},{"name":"mixed germ cell tumor of central nervous system of adults","type":"exact"},{"name":"mixed germ cell tumour of central nervous system of adults","type":"exact"}],"termid":"MONDO:0004406","xrefs":{"Monarch":{"xref_id":"0004406"}}}


id: PBO:0066005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ral guanine nucleotide dissociation stimulator","termid":"PBO:0066005"}


id: FYPO:0005625
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a normal proportion of cells in the population remains viable after exposure to ultraviolet light during S phase of the mitotic cell cycle.","definition_xrefs":["PMID:26652183","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal viability following cellular response to UV","termid":"FYPO:0004662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000003","FYPO:0002057"],"is_obsolete":false,"name":"normal viability following cellular response to UV during mitotic S phase","synonyms":[{"name":"normal cell population viability following cellular response to UV during mitotic S phase","type":"exact"},{"name":"normal viability following UV exposure during mitotic S phase","type":"exact"},{"name":"normal viability following cellular response to UV during S phase of mitotic cell cycle","type":"exact"},{"name":"normal viability following cellular response to ultraviolet light during mitotic S phase","type":"exact"}],"termid":"FYPO:0005625"}


id: PBO:0090292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G1/S-specific B-type cyclin Cig1","termid":"PBO:0090292"}


id: MONDO:0021157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cervicitis","termid":"MONDO:0002345"},{"relation_name":"is_a","term_name":"gonorrhea","termid":"MONDO:0004277"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gonococcal cervicitis","secondary_identifiers":["SCTID:237083000","UMLS:C0812378","icd11.foundation:1706835456","MEDGEN:678343"],"synonyms":[{"name":"gonorrhea of cervix","type":"exact"},{"name":"gonorrhea of uterine cervix","type":"exact"},{"name":"gonorrhoea of cervix","type":"exact"},{"name":"gonorrhoea of uterine cervix","type":"exact"}],"termid":"MONDO:0021157","xrefs":{"Monarch":{"xref_id":"0021157"}}}


id: GO:0072518
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Rho GTPase-dependent catalysis of the reaction: ATP + a protein = ADP + a phosphoprotein.","definition_xrefs":["PMID:20230755","GOC:ecd","PMID:12778124"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0004672","GO:0140096","GO:0003674","GO:0003824","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"Rho-dependent protein serine/threonine kinase activity","synonyms":[{"name":"ROCK kinase activity","type":"exact"},{"name":"Rho-associated protein kinase activity","type":"exact"}],"termid":"GO:0072518"}


id: PBO:0017845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cationic amino acid transmembrane transporter Cat1","termid":"PBO:0017845"}


id: GO:0043232
data:
  {"annotated_genes":["SJAG_04992","SJAG_00423","SJAG_03143","SJAG_02465","SJAG_04493","SJAG_01787","SJAG_05307","SJAG_04880","SJAG_03745","SJAG_02198","SJAG_00663","SJAG_01804","SJAG_02543","SJAG_01377","SJAG_03122","SJAG_02071","SJAG_04388","SJAG_02248","SJAG_02643","SJAG_03696","SJAG_02469","SJAG_02652","SJAG_00611","SJAG_06110","SJAG_02372","SJAG_00930","SJAG_00118","SJAG_04623","SJAG_04817","SJAG_02224","SJAG_02452","SJAG_01752","SJAG_01760","SJAG_03126","SJAG_04940","SJAG_01354","SJAG_01823","SJAG_04004","SJAG_03719","SJAG_05216","SJAG_04173","SJAG_02592","SJAG_04097","SJAG_02879","SJAG_00363","SJAG_03345","SJAG_03698","SJAG_01056","SJAG_00641","SJAG_04558","SJAG_00918","SJAG_02417","SJAG_00332","SJAG_00336","SJAG_03424","SJAG_00844","SJAG_02444","SJAG_03810","SJAG_02990","SJAG_04839","SJAG_00871","SJAG_00748","SJAG_04039","SJAG_02556","SJAG_03484","SJAG_01632","SJAG_00344","SJAG_02278","SJAG_02212","SJAG_04712","SJAG_02081","SJAG_02708","SJAG_02201","SJAG_03234","SJAG_01889","SJAG_00856","SJAG_02777","SJAG_01662","SJAG_02798","SJAG_04191","SJAG_04020","SJAG_00584","SJAG_02644","SJAG_01623","SJAG_04491","SJAG_05247","SJAG_04995","SJAG_04141","SJAG_04893","SJAG_02980","SJAG_02566","SJAG_01419","SJAG_00940","SJAG_01807","SJAG_01734","SJAG_00069","SJAG_04524","SJAG_01215","SJAG_00845","SJAG_02263","SJAG_01454","SJAG_00440","SJAG_00970","SJAG_04465","SJAG_00701","SJAG_00536","SJAG_06560","SJAG_04281","SJAG_00943","SJAG_03708","SJAG_03410","SJAG_01272","SJAG_01444","SJAG_00441","SJAG_00896","SJAG_02536","SJAG_03564","SJAG_03731","SJAG_00769","SJAG_02701","SJAG_03454","SJAG_03689","SJAG_00794","SJAG_00879","SJAG_04381","SJAG_05273","SJAG_01082","SJAG_01606","SJAG_03387","SJAG_04508","SJAG_02597","SJAG_02329","SJAG_03425","SJAG_04581","SJAG_03217","SJAG_00323","SJAG_01813","SJAG_04993","SJAG_03145","SJAG_01818","SJAG_04244","SJAG_01366","SJAG_00306","SJAG_03638","SJAG_03576","SJAG_02700","SJAG_01546","SJAG_02314","SJAG_02347","SJAG_02186","SJAG_00155","SJAG_03628","SJAG_03455","SJAG_04372","SJAG_02335","SJAG_00983","SJAG_01495","SJAG_01009","SJAG_04919","SJAG_02530","SJAG_01694","SJAG_03252","SJAG_02755","SJAG_01648","SJAG_00913","SJAG_03776","SJAG_01143","SJAG_01719","SJAG_04253","SJAG_02724","SJAG_04877","SJAG_01153","SJAG_05694","SJAG_01878","SJAG_02864","SJAG_01182","SJAG_01152","SJAG_02761","SJAG_03360","SJAG_00600","SJAG_01777","SJAG_00806","SJAG_04480","SJAG_05196","SJAG_01262","SJAG_01478","SJAG_02899","SJAG_02736","SJAG_01769","SJAG_02332","SJAG_04607","SJAG_00897","SJAG_00581","SJAG_00684","SJAG_00250","SJAG_02490","SJAG_04303","SJAG_00854","SJAG_04943","SJAG_02287","SJAG_01087","SJAG_02213","SJAG_03702","SJAG_04527","SJAG_04006","SJAG_02270","SJAG_02075","SJAG_02245","SJAG_04478","SJAG_03419","SJAG_00966","SJAG_00628","SJAG_16457","SJAG_03053","SJAG_02747","SJAG_00207","SJAG_03298","SJAG_04624","SJAG_02267","SJAG_02087","SJAG_05270","SJAG_00637","SJAG_01473","SJAG_02561","SJAG_03092","SJAG_01187","SJAG_00944","SJAG_01764","SJAG_04609","SJAG_03508","SJAG_02362","SJAG_04814","SJAG_00503","SJAG_03097","SJAG_04252","SJAG_00429","SJAG_03584","SJAG_03625","SJAG_01323","SJAG_05190","SJAG_01625","SJAG_02873","SJAG_02458","SJAG_03957","SJAG_04140","SJAG_03216","SJAG_03599","SJAG_00350","SJAG_01385","SJAG_03423","SJAG_02098","SJAG_02952","SJAG_05019","SJAG_00868","SJAG_02866","SJAG_04746","SJAG_04745","SJAG_04378","SJAG_01378","SJAG_00765","SJAG_04375","SJAG_01907","SJAG_02500","SJAG_04076","SJAG_03214","SJAG_02058","SJAG_04293","SJAG_02707","SJAG_02318","SJAG_02626","SJAG_02926","SJAG_01732","SJAG_01888","SJAG_02821","SJAG_02294","SJAG_04092","SJAG_05373","SJAG_02239","SJAG_03127","SJAG_02585","SJAG_02616","SJAG_04177","SJAG_00926","SJAG_05295","SJAG_03542","SJAG_03597","SJAG_02900","SJAG_03758","SJAG_04194","SJAG_03923","SJAG_02628","SJAG_02378","SJAG_02320","SJAG_03567","SJAG_05006","SJAG_04982","SJAG_03264","SJAG_00609","SJAG_04143","SJAG_01242","SJAG_02814","SJAG_01193","SJAG_02508","SJAG_04128","SJAG_04596","SJAG_00421","SJAG_02869","SJAG_00741","SJAG_03040","SJAG_01650","SJAG_02540","SJAG_00700","SJAG_03901","SJAG_04980","SJAG_00722","SJAG_01707","SJAG_02281","SJAG_04755","SJAG_04669","SJAG_00726","SJAG_01712","SJAG_00873","SJAG_00335","SJAG_01370","SJAG_04142","SJAG_03042","SJAG_00430","SJAG_04461","SJAG_02778","SJAG_04696","SJAG_02836","SJAG_06612","SJAG_04689","SJAG_01790","SJAG_04908","SJAG_03441","SJAG_02870","SJAG_00743","SJAG_03346","SJAG_03646","SJAG_04052","SJAG_03884","SJAG_01205","SJAG_03375","SJAG_01296","SJAG_02373","SJAG_01176","SJAG_04753","SJAG_00377","SJAG_00616","SJAG_02513","SJAG_01877","SJAG_01674","SJAG_03436","SJAG_00982","SJAG_00259","SJAG_00728","SJAG_02894","SJAG_00187","SJAG_03254","SJAG_03682","SJAG_01676","SJAG_04650","SJAG_02680","SJAG_02172","SJAG_04724","SJAG_04974","SJAG_00677","SJAG_02531","SJAG_04272","SJAG_01565","SJAG_03422","SJAG_02477","SJAG_00030","SJAG_04512","SJAG_06270","SJAG_04224","SJAG_00579","SJAG_01831","SJAG_05253","SJAG_01494","SJAG_04207","SJAG_05319","SJAG_05276","SJAG_04310","SJAG_02072","SJAG_01634","SJAG_04121","SJAG_04816","SJAG_03192","SJAG_04081","SJAG_03876","SJAG_03844","SJAG_01364","SJAG_02385","SJAG_03028","SJAG_04479","SJAG_02872","SJAG_02396","SJAG_04921","SJAG_01575","SJAG_03277","SJAG_02718","SJAG_05329","SJAG_02250","SJAG_04994","SJAG_00583","SJAG_04918","SJAG_02303","SJAG_01938","SJAG_04654","SJAG_04187","SJAG_01468","SJAG_01188","SJAG_04468","SJAG_03581","SJAG_04346","SJAG_04998","SJAG_00184","SJAG_00697","SJAG_03720","SJAG_02401","SJAG_03326","SJAG_03997","SJAG_00640","SJAG_02835","SJAG_03471","SJAG_02089","SJAG_00887","SJAG_00739","SJAG_00436","SJAG_00105","SJAG_03052","SJAG_03680","SJAG_05232","SJAG_05105","SJAG_00958","SJAG_03789","SJAG_02890","SJAG_01297","SJAG_00034","SJAG_01613","SJAG_07002","SJAG_01303","SJAG_02723","SJAG_00271","SJAG_03080","SJAG_00629","SJAG_01529","SJAG_01463","SJAG_02759","SJAG_04168","SJAG_02040","SJAG_05205","SJAG_01943","SJAG_02923","SJAG_01250","SJAG_00303","SJAG_05315","SJAG_02286","SJAG_00327","SJAG_03197","SJAG_03673","SJAG_00317","SJAG_03751","SJAG_03699","SJAG_04638","SJAG_00418","SJAG_04055","SJAG_05265","SJAG_01230","SJAG_04324","SJAG_01708","SJAG_02891","SJAG_04100","SJAG_03020","SJAG_02610","SJAG_05197","SJAG_03421","SJAG_02509","SJAG_03047","SJAG_02070","SJAG_00920","SJAG_03374","SJAG_03583","SJAG_03897","SJAG_04610","SJAG_03694","SJAG_02074","SJAG_04190","SJAG_01548","SJAG_00198","SJAG_00269","SJAG_03794","SJAG_03931","SJAG_04280","SJAG_01146","SJAG_03320","SJAG_00166","SJAG_03905","SJAG_00572","SJAG_00986","SJAG_02576","SJAG_05264","SJAG_00545","SJAG_04455","SJAG_03874","SJAG_04038","SJAG_04186","SJAG_03570","SJAG_00692","SJAG_02651","SJAG_05288","SJAG_00655","SJAG_02511","SJAG_02189","SJAG_04847","SJAG_03525","SJAG_02312","SJAG_02725","SJAG_03936","SJAG_03703","SJAG_01954","SJAG_04490","SJAG_02731","SJAG_01122","SJAG_05153","SJAG_00689","SJAG_00945","SJAG_03815","SJAG_01573","SJAG_04644","SJAG_01992","SJAG_02828","SJAG_03413","SJAG_00925","SJAG_03073","SJAG_03353","SJAG_01785","SJAG_01622","SJAG_01046","SJAG_00311","SJAG_01203","SJAG_02682","SJAG_00735","SJAG_01084","SJAG_02209","SJAG_02664","SJAG_03132","SJAG_05321","SJAG_03540","SJAG_01887","SJAG_02838","SJAG_01624","SJAG_03033","SJAG_02549","SJAG_01630","SJAG_01026","SJAG_03116","SJAG_00746","SJAG_03157","SJAG_00840","SJAG_03041","SJAG_01431","SJAG_02720","SJAG_04551","SJAG_02479","SJAG_00384","SJAG_01713","SJAG_03402","SJAG_00696","SJAG_03519","SJAG_04457","SJAG_01365","SJAG_04680","SJAG_02377","SJAG_00768","SJAG_03792","SJAG_03501","SJAG_01605","SJAG_00460","SJAG_04088","SJAG_01401","SJAG_00773","SJAG_03989","SJAG_02253","SJAG_06642","SJAG_02818","SJAG_05301","SJAG_00229","SJAG_00471","SJAG_03891","SJAG_02573","SJAG_00884","SJAG_04663","SJAG_03887","SJAG_00221","SJAG_00544","SJAG_01486","SJAG_01829","SJAG_04748","SJAG_04841","SJAG_03927","SJAG_00391","SJAG_03627","SJAG_03146","SJAG_00083","SJAG_01849","SJAG_05012","SJAG_01739","SJAG_03487","SJAG_04210","SJAG_01280","SJAG_02541","SJAG_02200","SJAG_03061","SJAG_04766","SJAG_04977","SJAG_00474","SJAG_04257","SJAG_02907","SJAG_02638","SJAG_04089","SJAG_01721","SJAG_04567","SJAG_00447","SJAG_01322","SJAG_03867","SJAG_02237","SJAG_01017","SJAG_00302","SJAG_03602","SJAG_03200","SJAG_01533","SJAG_05285","SJAG_01465","SJAG_02886","SJAG_01234","SJAG_00220","SJAG_03543","SJAG_02547","SJAG_03088","SJAG_02768","SJAG_04256","SJAG_00507","SJAG_01132","SJAG_03376","SJAG_02472","SJAG_04815","SJAG_00159","SJAG_02518","SJAG_02667","SJAG_02243","SJAG_03915","SJAG_02754","SJAG_04464","SJAG_02447","SJAG_03259","SJAG_01873","SJAG_03617","SJAG_00483","SJAG_05248","SJAG_01563","SJAG_00729","SJAG_04884","SJAG_03379","SJAG_02431","SJAG_04083","SJAG_04069","SJAG_04160","SJAG_01948","SJAG_04767","SJAG_00935","SJAG_03086","SJAG_02510","SJAG_01680","SJAG_01837","SJAG_02662","SJAG_02695","SJAG_04498","SJAG_04066","SJAG_01822","SJAG_01897","SJAG_00086","SJAG_03942","SJAG_02995","SJAG_00961","SJAG_01479","SJAG_00514","SJAG_00750","SJAG_02037","SJAG_02045","SJAG_01186","SJAG_02025","SJAG_02622","SJAG_04613","SJAG_02073","SJAG_04427","SJAG_00819","SJAG_01325","SJAG_01111","SJAG_04341","SJAG_03133","SJAG_01036","SJAG_MIT07","SJAG_02326","SJAG_03128","SJAG_00564","SJAG_04164","SJAG_01581","SJAG_03411","SJAG_04916","SJAG_03840","SJAG_03065","SJAG_01964","SJAG_02202","SJAG_02035","SJAG_03982","SJAG_01601","SJAG_04509","SJAG_05313","SJAG_02921","SJAG_02226","SJAG_00838","SJAG_01327","SJAG_02527","SJAG_04626","SJAG_05185","SJAG_05218","SJAG_04917","SJAG_03366","SJAG_02368","SJAG_00145","SJAG_03350","SJAG_04195","SJAG_02499","SJAG_02319","SJAG_05180","SJAG_05237","SJAG_03944","SJAG_03156","SJAG_03016","SJAG_02207","SJAG_03418","SJAG_03843","SJAG_16455","SJAG_02464","SJAG_02546","SJAG_04350","SJAG_04494","SJAG_04259","SJAG_03025","SJAG_00646","SJAG_02409","SJAG_00247","SJAG_02829","SJAG_01557","SJAG_02067","SJAG_03262","SJAG_03594","SJAG_03220","SJAG_00272","SJAG_00342","SJAG_01005","SJAG_03431","SJAG_03877","SJAG_00087","SJAG_04477","SJAG_02170","SJAG_02849","SJAG_03654","SJAG_02460","SJAG_04582","SJAG_02182","SJAG_00719","SJAG_06635","SJAG_03615","SJAG_02161","SJAG_00618","SJAG_02514","SJAG_04188","SJAG_02659","SJAG_00800","SJAG_04656","SJAG_04561","SJAG_02246","SJAG_01579","SJAG_04671","SJAG_03023","SJAG_04530","SJAG_02553","SJAG_03043","SJAG_00333","SJAG_02927","SJAG_00537","SJAG_03872","SJAG_04153","SJAG_02283","SJAG_03437","SJAG_03685","SJAG_04239","SJAG_02697","SJAG_00798","SJAG_05186","SJAG_02863","SJAG_02830","SJAG_05979","SJAG_02300","SJAG_04216","SJAG_02810","SJAG_05192","SJAG_02184","SJAG_00465","SJAG_04412","SJAG_03449","SJAG_04255","SJAG_01520","SJAG_03683","SJAG_00733","SJAG_03459","SJAG_04395","SJAG_01278","SJAG_04355","SJAG_01476","SJAG_04932","SJAG_03235","SJAG_02340","SJAG_04547","SJAG_02416","SJAG_01159","SJAG_02382","SJAG_00889","SJAG_00472","SJAG_00942","SJAG_06022","SJAG_04653","SJAG_04470","SJAG_00857","SJAG_02177","SJAG_04019","SJAG_01211","SJAG_01698","SJAG_00796","SJAG_04936","SJAG_02419","SJAG_04532","SJAG_03911","SJAG_01611","SJAG_04030","SJAG_02773","SJAG_01169","SJAG_02439","SJAG_02101","SJAG_07011","SJAG_04174","SJAG_00307","SJAG_00266","SJAG_05320","SJAG_03383","SJAG_05978","SJAG_02121","SJAG_04911","SJAG_01002","SJAG_02311","SJAG_05679","SJAG_05372","SJAG_01049","SJAG_02702","SJAG_04206","SJAG_01410","SJAG_04201","SJAG_05338","SJAG_02758","SJAG_04106","SJAG_04989","SJAG_04973","SJAG_02808","SJAG_03458","SJAG_02241","SJAG_00111","SJAG_05244","SJAG_03624","SJAG_03062","SJAG_04640","SJAG_03971","SJAG_00290","SJAG_02653","SJAG_02563","SJAG_04672","SJAG_02427","SJAG_02535","SJAG_00521","SJAG_04176","SJAG_00667","SJAG_00202","SJAG_00142","SJAG_02487","SJAG_00150","SJAG_01175","SJAG_06253","SJAG_03888","SJAG_04342","SJAG_03491","SJAG_02280","SJAG_00268","SJAG_00178","SJAG_01653","SJAG_01836","SJAG_03952","SJAG_03619","SJAG_04407","SJAG_03649","SJAG_00939","SJAG_04204","SJAG_03144","SJAG_01936","SJAG_00140","SJAG_01776","SJAG_01928","SJAG_01267","SJAG_03916","SJAG_02266","SJAG_02737","SJAG_04931","SJAG_04150","SJAG_00772","SJAG_05010","SJAG_00678","SJAG_00783","SJAG_03909","SJAG_02097","SJAG_00731","SJAG_00475","SJAG_01062","SJAG_04601","SJAG_01224","SJAG_00799","SJAG_04183","SJAG_00932","SJAG_00712","SJAG_03044","SJAG_00666","SJAG_06597","SJAG_00253","SJAG_03070","SJAG_03722","SJAG_00077","SJAG_03230","SJAG_04575","SJAG_00657","SJAG_04033","SJAG_01839","SJAG_01910","SJAG_04308","SJAG_00245","SJAG_02681","SJAG_05309","SJAG_00349","SJAG_03921","SJAG_07009","SJAG_02690","SJAG_00682","SJAG_00411","SJAG_01762","SJAG_02621","SJAG_05353","SJAG_04077","SJAG_03551","SJAG_01076","SJAG_05282","SJAG_02228","SJAG_01867","SJAG_05193","SJAG_00676","SJAG_01053","SJAG_00320","SJAG_01232","SJAG_03438","SJAG_02451","SJAG_01509","SJAG_03289","SJAG_03048","SJAG_01853","SJAG_02282","SJAG_04476","SJAG_02807","SJAG_01538","SJAG_01540","SJAG_02803","SJAG_03906","SJAG_00562","SJAG_05207","SJAG_03666","SJAG_03954","SJAG_01717","SJAG_01775","SJAG_02775","SJAG_02163","SJAG_00782","SJAG_00356","SJAG_02232","SJAG_03380","SJAG_02486","SJAG_03077","SJAG_04005","SJAG_01307","SJAG_01067","SJAG_02813","SJAG_00523","SJAG_03635","SJAG_03479","SJAG_02645","SJAG_01375","SJAG_01475","SJAG_03892","SJAG_02254","SJAG_01287","SJAG_00686","SJAG_04126","SJAG_03612","SJAG_03554","SJAG_00792","SJAG_03335","SJAG_00294","SJAG_00163","SJAG_00538","SJAG_04274","SJAG_05220","SJAG_03161","SJAG_00228","SJAG_01756","SJAG_04934","SJAG_03704","SJAG_05290","SJAG_04566","SJAG_01711","SJAG_03939","SJAG_04396","SJAG_02169","SJAG_03713","SJAG_01016","SJAG_03604","SJAG_04339","SJAG_04180","SJAG_04781","SJAG_00399","SJAG_00861","SJAG_03183","SJAG_02749","SJAG_04041","SJAG_04534","SJAG_04424","SJAG_04670","SJAG_03357","SJAG_01202","SJAG_02600","SJAG_02104","SJAG_03668","SJAG_00060","SJAG_03728","SJAG_01993","SJAG_02911","SJAG_01609","SJAG_03752","SJAG_03006","SJAG_02545","SJAG_04886","SJAG_01114","SJAG_02521","SJAG_05001","SJAG_MIT05","SJAG_01384","SJAG_03846","SJAG_00955","SJAG_03796","SJAG_00617","SJAG_02771","SJAG_03695","SJAG_00410","SJAG_03466","SJAG_00759","SJAG_02840","SJAG_02194","SJAG_03495","SJAG_01580","SJAG_02394","SJAG_02522","SJAG_03034","SJAG_03681","SJAG_03193","SJAG_02607","SJAG_05260","SJAG_01277","SJAG_04492","SJAG_03465","SJAG_03342","SJAG_02922","SJAG_02165","SJAG_00764","SJAG_00526","SJAG_01332","SJAG_02348","SJAG_01391","SJAG_00693","SJAG_04304","SJAG_02663","SJAG_00378","SJAG_03453","SJAG_04040","SJAG_00807","SJAG_01821","SJAG_01313","SJAG_03636","SJAG_05331","SJAG_03609","SJAG_00934","SJAG_00369","SJAG_04791","SJAG_04700","SJAG_04758","SJAG_00213","SJAG_01748","SJAG_01811","SJAG_04001","SJAG_04703","SJAG_00100","SJAG_04597","SJAG_00293","SJAG_00757","SJAG_00863","SJAG_04036","SJAG_02904","SJAG_00153","SJAG_04950","SJAG_01045","SJAG_01413","SJAG_02861","SJAG_01282","SJAG_01347","SJAG_02812","SJAG_02242","SJAG_03036","SJAG_00756","SJAG_03568","SJAG_04576","SJAG_04574","SJAG_04261","SJAG_04586","SJAG_01204","SJAG_00814","SJAG_00364","SJAG_03356","SJAG_03839","SJAG_03898","SJAG_01387","SJAG_02560","SJAG_00170","SJAG_00744","SJAG_00882","SJAG_04979","SJAG_03762","SJAG_05266","SJAG_02262","SJAG_03255","SJAG_02079","SJAG_03176","SJAG_04084","SJAG_02506","SJAG_04889","SJAG_04400","SJAG_04245","SJAG_00566","SJAG_01658","SJAG_01665","SJAG_00594","SJAG_04754","SJAG_04879","SJAG_00497","SJAG_00285","SJAG_02066","SJAG_03067","SJAG_01513","SJAG_00047","SJAG_01761","SJAG_05573","SJAG_00414","SJAG_03498","SJAG_03008","SJAG_00585","SJAG_01916","SJAG_00874","SJAG_00910","SJAG_02609","SJAG_04517","SJAG_03283","SJAG_02871","SJAG_00883","SJAG_01157","SJAG_04414","SJAG_02981","SJAG_00841","SJAG_01422","SJAG_05333","SJAG_03688","SJAG_00104","SJAG_03578","SJAG_05173","SJAG_04813","SJAG_00456","SJAG_03433","SJAG_00054","SJAG_16454","SJAG_05323","SJAG_02020","SJAG_03631","SJAG_00279","SJAG_01864","SJAG_00860","SJAG_03984","SJAG_01075","SJAG_03780","SJAG_04389","SJAG_02550","SJAG_00949","SJAG_02529","SJAG_04599","SJAG_04621","SJAG_03603","SJAG_04901","SJAG_00907","SJAG_00698","SJAG_02346","SJAG_02575","SJAG_01191","SJAG_05187","SJAG_02046","SJAG_02762","SJAG_01228","SJAG_03451","SJAG_02359","SJAG_04213","SJAG_04062","SJAG_03179","SJAG_00723","SJAG_01369","SJAG_01420","SJAG_00921","SJAG_03922","SJAG_02589","SJAG_03832","SJAG_04887","SJAG_00541","SJAG_02624","SJAG_01915","SJAG_01551","SJAG_01125","SJAG_01568","SJAG_04897","SJAG_02800","SJAG_01110","SJAG_04330","SJAG_02846","SJAG_02475","SJAG_00510","SJAG_03159","SJAG_03544","SJAG_03113","SJAG_03221","SJAG_03926","SJAG_04003","SJAG_01010","SJAG_03592","SJAG_00405","SJAG_01429","SJAG_02094","SJAG_02629","SJAG_03460","SJAG_04666","SJAG_01926","SJAG_02571","SJAG_03364","SJAG_01745","SJAG_07018","SJAG_00749","SJAG_00113","SJAG_04699","SJAG_03285","SJAG_00965","SJAG_03468","SJAG_04788","SJAG_01050","SJAG_00397","SJAG_03163","SJAG_01620","SJAG_03945","SJAG_06613","SJAG_02082","SJAG_04863","SJAG_03855","SJAG_03859","SJAG_04744","SJAG_00851","SJAG_02698","SJAG_04595","SJAG_02119","SJAG_04056","SJAG_04010","SJAG_03011","SJAG_01226","SJAG_01498","SJAG_02544","SJAG_02013","SJAG_01599","SJAG_01562","SJAG_03388","SJAG_03730","SJAG_02606","SJAG_02381","SJAG_04768","SJAG_00315","SJAG_01767","SJAG_02324","SJAG_03981","SJAG_01832","SJAG_03351","SJAG_04108","SJAG_03630","SJAG_04929","SJAG_07014","SJAG_01483","SJAG_02299","SJAG_03164","SJAG_03919","SJAG_04289","SJAG_03787","SJAG_00624","SJAG_05239","SJAG_03297","SJAG_00152","SJAG_01317","SJAG_03835","SJAG_01727","SJAG_01128","SJAG_04436","SJAG_01677","SJAG_MIT06","SJAG_00813","SJAG_02906","SJAG_03327","SJAG_01799","SJAG_00987","SJAG_01588","SJAG_00468","SJAG_01765","SJAG_01512","SJAG_02466","SJAG_01608","SJAG_03569","SJAG_01675","SJAG_04695","SJAG_02542","SJAG_01894","SJAG_03286","SJAG_04692","SJAG_00172","SJAG_04772","SJAG_01194","SJAG_01988","SJAG_03430","SJAG_00649","SJAG_01436","SJAG_03444","SJAG_04074","SJAG_03956","SJAG_01591","SJAG_04562","SJAG_02043","SJAG_02802","SJAG_07013","SJAG_02795","SJAG_02790","SJAG_03284","SJAG_04029","SJAG_01196","SJAG_05020","SJAG_01222","SJAG_01464","SJAG_02627","SJAG_02908","SJAG_03287","SJAG_00938","SJAG_03596","SJAG_00082","SJAG_04793","SJAG_02187","SJAG_01330","SJAG_01604","SJAG_01275","SJAG_01411","SJAG_01805","SJAG_02392","SJAG_00724","SJAG_04475","SJAG_01664","SJAG_03664","SJAG_00045","SJAG_04838","SJAG_03341","SJAG_03967","SJAG_03068","SJAG_03276","SJAG_03026","SJAG_01521","SJAG_02164","SJAG_03579","SJAG_01268","SJAG_01583","SJAG_03941","SJAG_04205","SJAG_01644","SJAG_02611","SJAG_00513","SJAG_03119","SJAG_02831","SJAG_02116","SJAG_01201","SJAG_04855","SJAG_04387","SJAG_01371","SJAG_01171","SJAG_01670","SJAG_00470","SJAG_00727","SJAG_02608","SJAG_04118","SJAG_01386","SJAG_02336","SJAG_00185","SJAG_00148"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[107057,103640,100764],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099079"},{"annotations":[91186],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030478"},{"annotations":[70955,75709,108960,112639,103641,104961,116294,78773,116861,97142,71843,70950,73937,102838,113627,79519,114124,107267,81984,69706,110997,108776,102806,114871,77793,76651,59219,118148,77018,120502,120866,76265,112980,66011,81083,104636,114151,101556,95489,67278,78629,104408,94419,99592,92493,64347,107076,80925,89958,107946,81369],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030479"},{"annotations":[82243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015629"},{"annotations":[77309,110998,73199,78502,97143],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005884"},{"annotations":[79027,121248,73197],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032432"},{"annotations":[121111,121113,121114,121247,121495,121112,121110],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005826"},{"annotations":[77010,74702,76619,72129],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005658"},{"annotations":[76652,81546,81825,78249,80082,80772,79571],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005885"},{"annotations":[101082,109353,114089,109139,105912],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000235"},{"annotations":[80715,61050],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990334"},{"annotations":[76262,79390,59436,82088],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031429"},{"annotations":[117096,97895],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015030"},{"annotations":[119139,93903,118502,108224,111609,93162,91881,113911],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061638"},{"annotations":[103956],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043505"},{"annotations":[110083,92603,119430,114141],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061838"},{"annotations":[100144,98732,101732],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061493"},{"annotations":[91466],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0005814"},{"annotations":[80721,74735,75662],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030896"},{"annotations":[68851,108346,68274,115813,94715,57206,64169,107308,108873,93368,105855,71857,108556,116059,91580,94826,102283,97546,90712,91910,108068,115491,120861,81749,108908,109762,100023,71604,102962,89213,90979,100017,103110,114774,115859,64981,99240,118518,121355,95899,113880,77657,107965,99161,68936,116233,91406,95574,80651,79961,105066,113502,74642,76159,95788,117684,98034,71938,90936,60638,106539,109164,98667,110572,111272,95776,90293,106197,96662,108976,109658,111436,117459,101820,58621,102106,96604,74273,111203,95554,97125,97767,81247,93085,102384,77684,82234,90198,101608,92243,90605,97659,99187,91074,96023,101502,59723,81935,93751,108926,109981,111067,113143,92020,99288,76276,109504,72157,111293,101232,110975,108850,113137,95799,114235,113859,92264,108237,115049,95131,90267,116773,117002,108748,118566,105453,99051,106765,66131,108655,110376,118329,111593,116643,58960,92156,98446,80418,112512,118475,111638,119323,99018,100006,112191,102183,118254,113341,115531,96205,119937,108504,111887,119472,92485,113598,100924,110448,119407,99105,101288,59012,96404,105073,103511,105884,109378,117858,119307,118448,81446,92532,106253,110988,113814,117081,118746,111260,120063,93549,104239,106876,107611,91391,105217,58743,114720,101060,80323,89184,100540,104854,113084,112970,114704,95986,101766,111130,114791,117411,119004,106120,108537,106348,100757,107541],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000785"},{"annotations":[103033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005694"},{"annotations":[78679,111158,75243,113852],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032133"},{"annotations":[113639,115347,118449,72278,91505,89805,90890,108113,116467,112259],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034506"},{"annotations":[111909,108190,71937,106404,60287,103157,113172,100925],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000775"},{"annotations":[118841,62278,108225,89671,120562,91867,113173,90891,61448,93164,110090,116255,116394,91176],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099115"},{"annotations":[121423,121268],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000781"},{"annotations":[60743,101433,109273,62024,93257,114897,90937,115253,108069,59456,64691,106049,59670,70944,90351,103025,72785,114059,94363,67417,113144,78971,106084,71320,58991,110091,120625,114894,118644,113682,108538,57698,67297,118297,114843,112163,114896,113490,67632,68692,71035,110053,100151,118228,114474,114895,101061,89200,60398,101334,93904,111048,114893,58840,58394,60147,114792,120084,101802,92453,104240,99289,102746],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140445"},{"annotations":[89288,100007,106198,113254,94071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071920"},{"annotations":[72212,119049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000793"},{"annotations":[100987,91883,93097,118842,92743,103960,109713,109749,89615,109666],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000779"},{"annotations":[82017,77550,76869,92744,80614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000794"},{"annotations":[78525,115348,73535,73925,57853],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000796"},{"annotations":[97224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030863"},{"annotations":[103318,101083,93207,100485,105782,110181],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0055028"},{"annotations":[89559,113360],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030981"},{"annotations":[99445,105644,97063],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903754"},{"annotations":[64218,112322],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990879"},{"annotations":[63441,79565,114705,71939,74406,78877,95800],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031390"},{"annotations":[79130,67388,81543,92813,67196],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005868"},{"annotations":[106779,106449,70159,92977,114729],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005881"},{"annotations":[102252],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905720"},{"annotations":[99139],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0062194"},{"annotations":[105784,98842,91441,104214,102253,116014,120659],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904511"},{"annotations":[93383,96408,78534,90168,75891,107587,113031,111831,76389,90975,91518,99658,101811,115590,68381,96641,91306,74774,80569,96207,81147,97946,96407,92089,74339,100801,119274,92013,89323,72346,94391,111933,115292,107234,107588,60504,94852,107494,57647,92131,91722,98979,108867,94851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010494"},{"annotations":[109266,93959,108145,111170,113312,103719,90664,104733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005856"},{"annotations":[72070,75093,78924,81849,92851,81999,79185,71895,80222,73645,78181,107567,69163,75562,118868,76680,73857,80225,79358,92852,77170,116456,116501,75820,64919,77961,81606,79938,71558,76127,76017,75362,114162,77179,98948,116500,76415,78237,74672,79823,89887,74972,76009,80855,75807,78154,73881,80173,73512,72053,72852,73034,75238,77540,77137,80935,96766,82178,107568,58341,75295,78591,96765,99031,73029,78616,76523,75982,114161,119417,73793,101041,79901,72922,73478,71932,73961,75811,72059,76487,78759,74207,73847],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022625"},{"annotations":[109829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0022626"},{"annotations":[115398,79011,107345,75209,107320,73678,76503,75143,75389,78421,80539,108635,107346,75488,76475,59126,103449,75509,75628,78929,101929,71717,76243,116174,80260,76284,76951,76320,72872,101670,76280,81898,80433,103448,72694,77699,71571,74997,101671,72170,81680,80144,77000,115396,81895,78433,75921,74521,76394,96615,72926,72940,76995,76222,116173,70372,77747,79411,93438,80904],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022627"},{"annotations":[64534,81454,76722,78313,63193,102405,64460,60952,69820,118901],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0042729"},{"annotations":[78649,76842,72733,104725],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043625"},{"annotations":[90640],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001651"},{"annotations":[82079,118230,78973],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005662"},{"annotations":[69065,113010,78419,82251,97065],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005869"},{"annotations":[93739,71532,73091],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036286"},{"annotations":[66001,79566,114794,74407,78878],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031391"},{"annotations":[109274,117383,115534,111889],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008622"},{"annotations":[104215,111546,114731,110786,102254,118923,101966,103320,112529,102870,108371,119177],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000923"},{"annotations":[108114,117960,113916,96180,66331,105313,108191,114008,113226,114061,115350,107294,115571],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000791"},{"annotations":[81985,80927],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008290"},{"annotations":[73161,79246],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035101"},{"annotations":[100157,110064,121625],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070648"},{"annotations":[101967,102871,80813,99518,108372,111547,119178,112530],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000931"},{"annotations":[102872,110788,112531,111548],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008275"},{"annotations":[81146,81764,72098,82046],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000811"},{"annotations":[117101,118924,110789,114605,111549,114807,112532],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061496"},{"annotations":[65488],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070823"},{"annotations":[101376,119173,106014,113840,90892,121288,98068,112165,90598,116550,96456,107295,116517,103393,95040,99081,109903],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000792"},{"annotations":[121293],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990343"},{"annotations":[120106,115254,94073,93098,119740,93698,95280,89289,120821,98100,100989,120086,92615,114062,118843],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990342"},{"annotations":[90240],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000123"},{"annotations":[121422],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140573"},{"annotations":[92815],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032117"},{"annotations":[76423,72970,95228,73053],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033503"},{"annotations":[117878,118645,115190,114144,101141,112261,116469],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000939"},{"annotations":[112533,104707,111550,102873,113390,110790],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061497"},{"annotations":[68135,78056,71635,73920,111001,90688,95850,103456,74677,89609,74385,57906,61672,115112,73518,117379,73395],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031011"},{"annotations":[98583,118925,111551,110791,104216,104708,102874,114732],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031021"},{"annotations":[98632,75598,77708,90771],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005871"},{"annotations":[105786,110183],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016938"},{"annotations":[74692,81669,91178,91807,115351,72288,111159,121250,106780,107391,96620,99141,113853,104243,66055,75241,114009,120862,101085,81236,81432,121354,105787,92604,77144,110184,98633,102019,78122,106451,117060],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000776"},{"annotations":[103228,115752],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0180019"},{"annotations":[93302,96605,111502,113086,106795,111595,90879,92158,117519],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030998"},{"annotations":[75751,116770,72660,119573,79050,67782,116160,96499,99553,80663,75717,91856,99642,100340,93732,76189,73227,91936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005811"},{"annotations":[119109,61224,98018,95917],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033193"},{"annotations":[116601,92668,94351,110004,103838,118155,95861,121627,90088,102033,90913,97227,113275,110065,103837,101429,95665],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990819"},{"annotations":[117948,107933,96354,101996],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032175"},{"annotations":[64577,117401,106085,115957,120564,114169,112245,112434,95918,61221,115019,98858,109586,119110,110092,92745,100990,105989,89672,89735,98597,101436,98019,114063,114563,73407,62280,74164,114562,119683,119741,119971,93099,120087,115255,116397,61450,95670,120822,111910],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031934"},{"annotations":[120646,119862,114743,58192,109890,103662,99691,101997,105819,102847],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0036391"},{"annotations":[109667,119050,89617,109750],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030893"},{"annotations":[107934,96355,101998,117949],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032152"},{"annotations":[104244,120662,113147,91179,115192,109751,117879,105175],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0072687"},{"annotations":[89561],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990574"},{"annotations":[118648,103321,105439,120698],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990385"},{"annotations":[93119,95704,101086,101784,109023,95631,104710,98634,120844,96622],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090619"},{"annotations":[89562,109024,107019,92816,101706,118910,112473,102830,101543,101804,102613,106031,113391,104817,104711,94129,91062,95705,94679,102735,101734,108310,110296,111552,113183,114606,115903,98635,96250,117451,95632,97066,99449,97168,93120,92544,98737,117102,113363,91582,89201,120135,101707,104245],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035974"},{"annotations":[98636,69569,75597,121351],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005874"},{"annotations":[96623,99142,106452,106781],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005875"},{"annotations":[74513,76408,76671,102457,74631,112712,79576,106991,79101,72469,77664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015630"},{"annotations":[102256,101088],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036449"},{"annotations":[80059,106232,101089],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005815"},{"annotations":[121307,81235,63004,106560,81797,101090,72452],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035371"},{"annotations":[101091],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005872"},{"annotations":[71609,76084,60695,81689],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000444"},{"annotations":[116111,96144,108289,115081,115522,96550,107464,99777,62474,91510,91862],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031511"},{"annotations":[101178,107860,90405,104775,121054,121055,104794,64565,121046],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000262"},{"annotations":[105585,118245,78415,71360,99834,73898,72503,79898,74556,81038,81198,107626,110166,79662,74817,113062,76579,99855,74222,98468,73568,112731,72945,114692,115419,79066,110017,111792,116690,118136,119911,68336,82229,80217,77381,81516,81652,116572,78386,114189,110116,77151,79926,108684],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005762"},{"annotations":[77505,103189,114031,90138,106052,112076,97604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042645"},{"annotations":[91779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005761"},{"annotations":[117995,93916,110281,112619,104207,75871,91753,96035,77494,97786,110021,74118,112084,108325,112336,114327,105906,70888,75919,74351,120079,96344,74983,78324,80127,98500,117574,99858,104981,99859,110527,107959],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005763"},{"annotations":[119629,121626,91147,91636,92545,78083,117796,94379,117880,95666,121229,108818,121234,121227,121232,103160,107271,112713,96432,100158,76703,120845,89695,103153,121236],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110085"},{"annotations":[111003,107063,102587,102421,119865],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120106"},{"annotations":[115327,108127,119883,105595,111004,97705,102820,119866,96797,92592,114268,99068,112754,98186,96252,91809,90085],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120105"},{"annotations":[58723,119021,118927,105821,80000,58191,99900,94162,99521,102000,102849,81556,110069,111005,108968],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120104"},{"annotations":[109668,73850,71670,92746],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030892"},{"annotations":[102001,102850,58193,105822],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032151"},{"annotations":[98637,64533,98342,102021,95779,113640,77579,74691,99248,97744,112520,108090,109677,105615,89809,110026,113893,98134,104341,91180,93145,107903,115375,90096,101515,100246,113458,102407,113401,66112,110643,108138,116987,93566,104795,91433,111160,101709,91684,70466,64459,94590,97898,117044,110969,111698,106162,111037,116518,97405,109159,101708,104947,116664,89399,91110,97068,113465,94765],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0072686"},{"annotations":[80623,63005,93211],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061673"},{"annotations":[98845],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905721"},{"annotations":[109433],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990941"},{"annotations":[108240,66683,103323,102258],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990498"},{"annotations":[78939,96625,93212,102423,113149,80619,102939,78016,91443,113855,120700,91811,95634,105441,92806,118649,119562,110188,104247],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990023"},{"annotations":[101093,109434,120139,100489],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990537"},{"annotations":[120140,102259],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097431"},{"annotations":[91434,92546,118496,110189,95577,99146,91063,109435,89202,94766,96097,98135,92807,96626,111503,112120,117881,104217,119285,100299,94130,105792,110699,93590,98256,101480,95099,102260,102487,114971,93213,112881,91949,115635,93012,99323,105720,108772,94365,96070,111911,72482,114439,98246,91468,96245,95780,92817,113459,117272,120768,121630,91812,108241,101968,108282,119179,70157,116932,105616,117984,66684,98187,95298,96253,98585,100490,110276,110684,112128,91566,99901,102022,114734,104948,102408,116665,113641,119191,121628,103514,106487,107400,90774,113011,116895,108373,119006,93167,121640,103161,116779,102424,72280,95635,110970,99676,118693,120224,98343,76436,98638,104036,107097,108557,102087,95719,111853,119265],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044732"},{"annotations":[70673,113642],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033551"},{"annotations":[80152,82003,77756],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034457"},{"annotations":[106339,101552,92577,107228],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036410"},{"annotations":[105152,97230,98739],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045160"},{"annotations":[81768,99523,73404,119869,74301],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016460"},{"annotations":[118158,110070],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031475"},{"annotations":[78916,77485,77647,76654],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031262"},{"annotations":[108312,113151,107273,101736,104713,112475,104249,92968,102832,109071],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071958"},{"annotations":[95795,108441,107229,109856],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033100"},{"annotations":[79632],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990467"},{"annotations":[100835,111006,74725,94211,81816,108803,75551,81944,78057,80861,74678,105937,79201,75425,69718,106630,80062],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035267"},{"annotations":[113424,114723,76154,76066,111205,77625,92617],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016604"},{"annotations":[89673,102468,70440,108540,112129,93596,104084,107993,95720,65387,98101,81165,97016,108115,112503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000228"},{"annotations":[70483,74404,114795,78240,78875,79563],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043599"},{"annotations":[109382,93699,113258,95282,120108,89293,106202,94075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990251"},{"annotations":[93214],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005880"},{"annotations":[75535,71703,76798,81315,62075,80547],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005664"},{"annotations":[115535,106053,97866,113346,113603,113228,105219,94398,99192,63579,61720,92488,104776,109275,106122,96927,92267,113862,120184,109767,79281,109987,102497,109659,114707,111890,115144,58529,57155,101179,101296,115123,96683,67298,105885,75621,94829,117384,61778],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043596"},{"annotations":[114476],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043601"},{"annotations":[104805,94203,97179,100425,108571,109723],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030874"},{"annotations":[72918,64489,73151,73497,101366,92917,106467,117284,120602,117372,60938],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005655"},{"annotations":[94846,117423,69449,77838,103574,93712,118860,90128,79410,115639,98540,117863,74575,108733,74427,74668,74623,108638,75519,78908,94491,106007,110108,93464,107569,116502,73337,97899,72087,74863,106204,94741,102290,101282,113856,93198,119636,102366,98120,117333,112594,74564,79859,98368,119419,70046,118567,92692,81354,102118,110264,112430,77681,115352,109206,109616,101489,107647,78833,118345,81957,121400,118911,78078,89400,119646,92855,115861,95127,108541,113904,120016,119763,104472,107321,115832,78009,119418,113175,78812,113984,116503,113306,75907,79275,72533,76890,116519,116528,116443,76108,72117,96975,101610,121352,105952,102359,76513,72352,74073,71684,81774,99367,115230,78967,90685,80072,78158,92653,95539,114258,100508,92856,105571,118845,75715,116701,74161,77205,104796,115401,118412,72461,107392,108637,76055,72693,81002,96976,115509,74589,76077,72320,72104,95969,107570,104060,78171,71787,72596,79304,116529,93482,72626,111520,81488,117334,102355,111492,97867,116328,118208,74507,80040,105268,102481,109928,80513,90603,108732,67428,119132,93231,59978,116912,73658,91767,72983,107591,113154,119647,80327,102925,80961,106762,103757,114846,98907,96169,74582,74614,75258,115286,93932,100661,74821,97490,109296,89495,89811,96741,106845,100509,75360,106324,117146,114477,112928,97662,109160,98251,107176,111038,100721,72339,106034,80443,107546,110953,76988,74134,75606,107666,107646,58517,101052,65196,73397,98326,99741,114011,101337,110470,103390,107592,90382,118535,79989,91869,92618,72292,99754,102530,74958,62174,114960,115987,108845,79738,81922,110265,116082,118327,74504,109383,73990,115400,74571,97582,81676,97282,81044,119595,78200,106006,73754,92854,114646,115549,120997,114064,79018,108267,113643,89888,89736,121353,79854,93059,97979,99840,107322,82184,113983,61655,111068,113167,114865,118181,96742,89552,78635,119216,80734,78326,92766,119966,108091,117049,114665,115399,91742,73482,105561,77112,80725],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005730"},{"annotations":[74954,114568,75539,114541,60873,78453,114543,114569,61557],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000786"},{"annotations":[101546,113157,108313,112536,104716,112477,116473,104252,106959,97498,114811,94681,109472,111555,110796],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071957"},{"annotations":[116474,120668,102262],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000940"},{"annotations":[110797,109026,118929],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061499"},{"annotations":[77800,78383,74898,92134,81499,114848,81433,77565,76000,118589,71978,78533,80678,81773,101813,75435,91520,117126,79559,80579,73456,81536,77246,79340,76358,71689,71665,72845,80583,74482,97451,81407,111834,79482,76164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000932"},{"annotations":[77975,75438,76602],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070545"},{"annotations":[89675,100992,109753,95672,116260,91871,109259,101486,93101,115959,98599,112436,89452,104677,105991,103731,108227,61452,117404,110094,94216,98021,118847,113169,101439,92748,114574,119974,115021,116399,120566,120824,95920,115641,116545,93172,91182,93906,114066,114575,117963,119112,100837,120088,106088,64579,114171,120702,62282,95936,115257,61223,115195,119743,119685,108470,93240],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005721"},{"annotations":[110191,105794],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005873"},{"annotations":[103326,96628],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005827"},{"annotations":[103327,98846],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905759"},{"annotations":[93216],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905760"},{"annotations":[105444,105795,110192],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990295"},{"annotations":[102003,96358,117951,107937],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0032169"},{"annotations":[81641,74880,62868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034515"},{"annotations":[94256,120590,60618,96893,106111,106915,111953,117481,118702,98404,102597,111954,92637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140453"},{"annotations":[81549,75354,78646,73139,73468],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034388"},{"annotations":[78876,95805,74405,90939,79564],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031389"},{"annotations":[62281,104169,91872,93702,114479,73408,61451,110095,115258,106089,118509,108228,118848,120825,113177,114067,115960,93173,116400],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033553"},{"annotations":[117255,101156,121424,103061],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030875"},{"annotations":[97868,96734,72166],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031422"},{"annotations":[80032,82169,101234],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031298"},{"annotations":[93102,120089,114172],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030958"},{"annotations":[77618,79268,69167,71838,92202,76948,72805,77511,78310,77304,104434,78733,58345,106802,117506,76295,75914,116193],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005736"},{"annotations":[81032,81665,77492],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070860"},{"annotations":[97436],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000120"},{"annotations":[80968,107193,73841,95015],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000500"},{"annotations":[79114,61488,77592,80761,64456,96494,77720,77911,63667,82058,90928,116211,108676],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033698"},{"annotations":[112427,80481,64457,77593,79917,82059,96495,61489,116121,79115,90929,106633,108677,76547,116212,95081,80762],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070210"},{"annotations":[74724,95622,97309,78362,74471,63666],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032221"},{"annotations":[74729,95852,59000,75444,81575,89466,67688,89968,95996,81437,72336,94134,97752,115096],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016586"},{"annotations":[78481,105263,73317,90305,119554,80665,77339,75550,75264,72679,58049,93241,62657,63935,75720,78938,113709,67685,118265],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000124"},{"annotations":[77214],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0005940"},{"annotations":[106090,80931,95082,80480,68367],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034967"},{"annotations":[96948,101600,81648,117922,93675,91586],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070187"},{"annotations":[114068,73409,110096,115259],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070824"},{"annotations":[117454,94682],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160065"},{"annotations":[100929,98785,77034,116261,109725,93261,113467,112775,104798,106330,106126,72875,78970,90982,95500,98036,105957,91415,113509,106056,118232,73443,104718,104856,102532,114481,91112,80719,92108,118498,120722,109679,118782,92024,99291,100838,111262,102941,105227,119193,102500,90445,113178,119709,93370,102470,101065,119287,75989,99021,94515,113685,109588,95782,98385,98991,79747,81182,77013,97869],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035861"},{"annotations":[58476,63937],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0046695"},{"annotations":[61026,67740],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033557"},{"annotations":[74255,76151,77036,119854,71962,89851,113448,76197],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030915"},{"annotations":[102877,80812],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0005819"},{"annotations":[63946,77581,78020,91569,78678,102410,105596],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005876"},{"annotations":[121594,121274,121251,121256],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005816"},{"annotations":[102852,103663],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032176"},{"annotations":[99150,103329,70154,116021,118930,66681,114735,102263],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099070"},{"annotations":[67239],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001725"},{"annotations":[72116],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0055120"},{"annotations":[115961,93909,117923,119686,100993,114173,120090,64575,95921,101440,120826,61219,114577,105992,115260,92749,98022,95673,106091,93103,112437,98600,119744,114069,119113,114578],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140720"},{"annotations":[109375,95977,78118,73073,71634,115097,89467,79451,74442,78815,97753,116989],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016514"},{"annotations":[109589,62538],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032798"},{"annotations":[89738,112248],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034974"},{"annotations":[109813,116694,94212,78055,78724,111009,115115,98520,74676,81815,75424,100108,115287,71828,100839,119440],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000812"},{"annotations":[74663,93882,78114,94479,112523,91059],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034455"},{"annotations":[109868],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000782"},{"annotations":[80350,79888,95581,77790,76351],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034456"}]},"cv_name":"cellular_component","definition":"Organized structure of distinctive morphology and function, not bounded by a lipid bilayer membrane and occurring within the cell. Includes ribosomes, the cytoskeleton and chromosomes.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membraneless organelle","termid":"GO:0043228"},{"relation_name":"is_a","term_name":"intracellular organelle","termid":"GO:0043229"}],"gene_count":1439,"genes_by_uniquename":{"SJAG_00030":null,"SJAG_00034":null,"SJAG_00045":null,"SJAG_00047":null,"SJAG_00054":null,"SJAG_00060":null,"SJAG_00069":null,"SJAG_00077":null,"SJAG_00082":null,"SJAG_00083":null,"SJAG_00086":null,"SJAG_00087":null,"SJAG_00100":null,"SJAG_00104":null,"SJAG_00105":null,"SJAG_00111":null,"SJAG_00113":null,"SJAG_00118":null,"SJAG_00140":null,"SJAG_00142":null,"SJAG_00145":null,"SJAG_00148":null,"SJAG_00150":null,"SJAG_00152":null,"SJAG_00153":null,"SJAG_00155":null,"SJAG_00159":null,"SJAG_00163":null,"SJAG_00166":null,"SJAG_00170":null,"SJAG_00172":null,"SJAG_00178":null,"SJAG_00184":null,"SJAG_00185":null,"SJAG_00187":null,"SJAG_00198":null,"SJAG_00202":null,"SJAG_00207":null,"SJAG_00213":null,"SJAG_00220":null,"SJAG_00221":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00245":null,"SJAG_00247":null,"SJAG_00250":null,"SJAG_00253":null,"SJAG_00259":null,"SJAG_00266":null,"SJAG_00268":null,"SJAG_00269":null,"SJAG_00271":null,"SJAG_00272":null,"SJAG_00279":null,"SJAG_00285":null,"SJAG_00290":null,"SJAG_00293":null,"SJAG_00294":null,"SJAG_00302":null,"SJAG_00303":null,"SJAG_00306":null,"SJAG_00307":null,"SJAG_00311":null,"SJAG_00315":null,"SJAG_00317":null,"SJAG_00320":null,"SJAG_00323":null,"SJAG_00327":null,"SJAG_00332":null,"SJAG_00333":null,"SJAG_00335":null,"SJAG_00336":null,"SJAG_00342":null,"SJAG_00344":null,"SJAG_00349":null,"SJAG_00350":null,"SJAG_00356":null,"SJAG_00363":null,"SJAG_00364":null,"SJAG_00369":null,"SJAG_00377":null,"SJAG_00378":null,"SJAG_00384":null,"SJAG_00391":null,"SJAG_00397":null,"SJAG_00399":null,"SJAG_00405":null,"SJAG_00410":null,"SJAG_00411":null,"SJAG_00414":null,"SJAG_00418":null,"SJAG_00421":null,"SJAG_00423":null,"SJAG_00429":null,"SJAG_00430":null,"SJAG_00436":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00447":null,"SJAG_00456":null,"SJAG_00460":null,"SJAG_00465":null,"SJAG_00468":null,"SJAG_00470":null,"SJAG_00471":null,"SJAG_00472":null,"SJAG_00474":null,"SJAG_00475":null,"SJAG_00483":null,"SJAG_00497":null,"SJAG_00503":null,"SJAG_00507":null,"SJAG_00510":null,"SJAG_00513":null,"SJAG_00514":null,"SJAG_00521":null,"SJAG_00523":null,"SJAG_00526":null,"SJAG_00536":null,"SJAG_00537":null,"SJAG_00538":null,"SJAG_00541":null,"SJAG_00544":null,"SJAG_00545":null,"SJAG_00562":null,"SJAG_00564":null,"SJAG_00566":null,"SJAG_00572":null,"SJAG_00579":null,"SJAG_00581":null,"SJAG_00583":null,"SJAG_00584":null,"SJAG_00585":null,"SJAG_00594":null,"SJAG_00600":null,"SJAG_00609":null,"SJAG_00611":null,"SJAG_00616":null,"SJAG_00617":null,"SJAG_00618":null,"SJAG_00624":null,"SJAG_00628":null,"SJAG_00629":null,"SJAG_00637":null,"SJAG_00640":null,"SJAG_00641":null,"SJAG_00646":null,"SJAG_00649":null,"SJAG_00655":null,"SJAG_00657":null,"SJAG_00663":null,"SJAG_00666":null,"SJAG_00667":null,"SJAG_00676":null,"SJAG_00677":null,"SJAG_00678":null,"SJAG_00682":null,"SJAG_00684":null,"SJAG_00686":null,"SJAG_00689":null,"SJAG_00692":null,"SJAG_00693":null,"SJAG_00696":null,"SJAG_00697":null,"SJAG_00698":null,"SJAG_00700":null,"SJAG_00701":null,"SJAG_00712":null,"SJAG_00719":null,"SJAG_00722":null,"SJAG_00723":null,"SJAG_00724":null,"SJAG_00726":null,"SJAG_00727":null,"SJAG_00728":null,"SJAG_00729":null,"SJAG_00731":null,"SJAG_00733":null,"SJAG_00735":null,"SJAG_00739":null,"SJAG_00741":null,"SJAG_00743":null,"SJAG_00744":null,"SJAG_00746":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00750":null,"SJAG_00756":null,"SJAG_00757":null,"SJAG_00759":null,"SJAG_00764":null,"SJAG_00765":null,"SJAG_00768":null,"SJAG_00769":null,"SJAG_00772":null,"SJAG_00773":null,"SJAG_00782":null,"SJAG_00783":null,"SJAG_00792":null,"SJAG_00794":null,"SJAG_00796":null,"SJAG_00798":null,"SJAG_00799":null,"SJAG_00800":null,"SJAG_00806":null,"SJAG_00807":null,"SJAG_00813":null,"SJAG_00814":null,"SJAG_00819":null,"SJAG_00838":null,"SJAG_00840":null,"SJAG_00841":null,"SJAG_00844":null,"SJAG_00845":null,"SJAG_00851":null,"SJAG_00854":null,"SJAG_00856":null,"SJAG_00857":null,"SJAG_00860":null,"SJAG_00861":null,"SJAG_00863":null,"SJAG_00868":null,"SJAG_00871":null,"SJAG_00873":null,"SJAG_00874":null,"SJAG_00879":null,"SJAG_00882":null,"SJAG_00883":null,"SJAG_00884":null,"SJAG_00887":null,"SJAG_00889":null,"SJAG_00896":null,"SJAG_00897":null,"SJAG_00907":null,"SJAG_00910":null,"SJAG_00913":null,"SJAG_00918":null,"SJAG_00920":null,"SJAG_00921":null,"SJAG_00925":null,"SJAG_00926":null,"SJAG_00930":null,"SJAG_00932":null,"SJAG_00934":null,"SJAG_00935":null,"SJAG_00938":null,"SJAG_00939":null,"SJAG_00940":null,"SJAG_00942":null,"SJAG_00943":null,"SJAG_00944":null,"SJAG_00945":null,"SJAG_00949":null,"SJAG_00955":null,"SJAG_00958":null,"SJAG_00961":null,"SJAG_00965":null,"SJAG_00966":null,"SJAG_00970":null,"SJAG_00982":null,"SJAG_00983":null,"SJAG_00986":null,"SJAG_00987":null,"SJAG_01002":null,"SJAG_01005":null,"SJAG_01009":null,"SJAG_01010":null,"SJAG_01016":null,"SJAG_01017":null,"SJAG_01026":null,"SJAG_01036":null,"SJAG_01045":null,"SJAG_01046":null,"SJAG_01049":null,"SJAG_01050":null,"SJAG_01053":null,"SJAG_01056":null,"SJAG_01062":null,"SJAG_01067":null,"SJAG_01075":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01087":null,"SJAG_01110":null,"SJAG_01111":null,"SJAG_01114":null,"SJAG_01122":null,"SJAG_01125":null,"SJAG_01128":null,"SJAG_01132":null,"SJAG_01143":null,"SJAG_01146":null,"SJAG_01152":null,"SJAG_01153":null,"SJAG_01157":null,"SJAG_01159":null,"SJAG_01169":null,"SJAG_01171":null,"SJAG_01175":null,"SJAG_01176":null,"SJAG_01182":null,"SJAG_01186":null,"SJAG_01187":null,"SJAG_01188":null,"SJAG_01191":null,"SJAG_01193":null,"SJAG_01194":null,"SJAG_01196":null,"SJAG_01201":null,"SJAG_01202":null,"SJAG_01203":null,"SJAG_01204":null,"SJAG_01205":null,"SJAG_01211":null,"SJAG_01215":null,"SJAG_01222":null,"SJAG_01224":null,"SJAG_01226":null,"SJAG_01228":null,"SJAG_01230":null,"SJAG_01232":null,"SJAG_01234":null,"SJAG_01242":null,"SJAG_01250":null,"SJAG_01262":null,"SJAG_01267":null,"SJAG_01268":null,"SJAG_01272":null,"SJAG_01275":null,"SJAG_01277":null,"SJAG_01278":null,"SJAG_01280":null,"SJAG_01282":null,"SJAG_01287":null,"SJAG_01296":null,"SJAG_01297":null,"SJAG_01303":null,"SJAG_01307":null,"SJAG_01313":null,"SJAG_01317":null,"SJAG_01322":null,"SJAG_01323":null,"SJAG_01325":null,"SJAG_01327":null,"SJAG_01330":null,"SJAG_01332":null,"SJAG_01347":null,"SJAG_01354":null,"SJAG_01364":null,"SJAG_01365":null,"SJAG_01366":null,"SJAG_01369":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01375":null,"SJAG_01377":null,"SJAG_01378":null,"SJAG_01384":null,"SJAG_01385":null,"SJAG_01386":null,"SJAG_01387":null,"SJAG_01391":null,"SJAG_01401":null,"SJAG_01410":null,"SJAG_01411":null,"SJAG_01413":null,"SJAG_01419":null,"SJAG_01420":null,"SJAG_01422":null,"SJAG_01429":null,"SJAG_01431":null,"SJAG_01436":null,"SJAG_01444":null,"SJAG_01454":null,"SJAG_01463":null,"SJAG_01464":null,"SJAG_01465":null,"SJAG_01468":null,"SJAG_01473":null,"SJAG_01475":null,"SJAG_01476":null,"SJAG_01478":null,"SJAG_01479":null,"SJAG_01483":null,"SJAG_01486":null,"SJAG_01494":null,"SJAG_01495":null,"SJAG_01498":null,"SJAG_01509":null,"SJAG_01512":null,"SJAG_01513":null,"SJAG_01520":null,"SJAG_01521":null,"SJAG_01529":null,"SJAG_01533":null,"SJAG_01538":null,"SJAG_01540":null,"SJAG_01546":null,"SJAG_01548":null,"SJAG_01551":null,"SJAG_01557":null,"SJAG_01562":null,"SJAG_01563":null,"SJAG_01565":null,"SJAG_01568":null,"SJAG_01573":null,"SJAG_01575":null,"SJAG_01579":null,"SJAG_01580":null,"SJAG_01581":null,"SJAG_01583":null,"SJAG_01588":null,"SJAG_01591":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01604":null,"SJAG_01605":null,"SJAG_01606":null,"SJAG_01608":null,"SJAG_01609":null,"SJAG_01611":null,"SJAG_01613":null,"SJAG_01620":null,"SJAG_01622":null,"SJAG_01623":null,"SJAG_01624":null,"SJAG_01625":null,"SJAG_01630":null,"SJAG_01632":null,"SJAG_01634":null,"SJAG_01644":null,"SJAG_01648":null,"SJAG_01650":null,"SJAG_01653":null,"SJAG_01658":null,"SJAG_01662":null,"SJAG_01664":null,"SJAG_01665":null,"SJAG_01670":null,"SJAG_01674":null,"SJAG_01675":null,"SJAG_01676":null,"SJAG_01677":null,"SJAG_01680":null,"SJAG_01694":null,"SJAG_01698":null,"SJAG_01707":null,"SJAG_01708":null,"SJAG_01711":null,"SJAG_01712":null,"SJAG_01713":null,"SJAG_01717":null,"SJAG_01719":null,"SJAG_01721":null,"SJAG_01727":null,"SJAG_01732":null,"SJAG_01734":null,"SJAG_01739":null,"SJAG_01745":null,"SJAG_01748":null,"SJAG_01752":null,"SJAG_01756":null,"SJAG_01760":null,"SJAG_01761":null,"SJAG_01762":null,"SJAG_01764":null,"SJAG_01765":null,"SJAG_01767":null,"SJAG_01769":null,"SJAG_01775":null,"SJAG_01776":null,"SJAG_01777":null,"SJAG_01785":null,"SJAG_01787":null,"SJAG_01790":null,"SJAG_01799":null,"SJAG_01804":null,"SJAG_01805":null,"SJAG_01807":null,"SJAG_01811":null,"SJAG_01813":null,"SJAG_01818":null,"SJAG_01821":null,"SJAG_01822":null,"SJAG_01823":null,"SJAG_01829":null,"SJAG_01831":null,"SJAG_01832":null,"SJAG_01836":null,"SJAG_01837":null,"SJAG_01839":null,"SJAG_01849":null,"SJAG_01853":null,"SJAG_01864":null,"SJAG_01867":null,"SJAG_01873":null,"SJAG_01877":null,"SJAG_01878":null,"SJAG_01887":null,"SJAG_01888":null,"SJAG_01889":null,"SJAG_01894":null,"SJAG_01897":null,"SJAG_01907":null,"SJAG_01910":null,"SJAG_01915":null,"SJAG_01916":null,"SJAG_01926":null,"SJAG_01928":null,"SJAG_01936":null,"SJAG_01938":null,"SJAG_01943":null,"SJAG_01948":null,"SJAG_01954":null,"SJAG_01964":null,"SJAG_01988":null,"SJAG_01992":null,"SJAG_01993":null,"SJAG_02013":null,"SJAG_02020":null,"SJAG_02025":null,"SJAG_02035":null,"SJAG_02037":null,"SJAG_02040":null,"SJAG_02043":null,"SJAG_02045":null,"SJAG_02046":null,"SJAG_02058":null,"SJAG_02066":null,"SJAG_02067":null,"SJAG_02070":null,"SJAG_02071":null,"SJAG_02072":null,"SJAG_02073":null,"SJAG_02074":null,"SJAG_02075":null,"SJAG_02079":null,"SJAG_02081":null,"SJAG_02082":null,"SJAG_02087":null,"SJAG_02089":null,"SJAG_02094":null,"SJAG_02097":null,"SJAG_02098":null,"SJAG_02101":null,"SJAG_02104":null,"SJAG_02116":null,"SJAG_02119":null,"SJAG_02121":null,"SJAG_02161":null,"SJAG_02163":null,"SJAG_02164":null,"SJAG_02165":null,"SJAG_02169":null,"SJAG_02170":null,"SJAG_02172":null,"SJAG_02177":null,"SJAG_02182":null,"SJAG_02184":null,"SJAG_02186":null,"SJAG_02187":null,"SJAG_02189":null,"SJAG_02194":null,"SJAG_02198":null,"SJAG_02200":null,"SJAG_02201":null,"SJAG_02202":null,"SJAG_02207":null,"SJAG_02209":null,"SJAG_02212":null,"SJAG_02213":null,"SJAG_02224":null,"SJAG_02226":null,"SJAG_02228":null,"SJAG_02232":null,"SJAG_02237":null,"SJAG_02239":null,"SJAG_02241":null,"SJAG_02242":null,"SJAG_02243":null,"SJAG_02245":null,"SJAG_02246":null,"SJAG_02248":null,"SJAG_02250":null,"SJAG_02253":null,"SJAG_02254":null,"SJAG_02262":null,"SJAG_02263":null,"SJAG_02266":null,"SJAG_02267":null,"SJAG_02270":null,"SJAG_02278":null,"SJAG_02280":null,"SJAG_02281":null,"SJAG_02282":null,"SJAG_02283":null,"SJAG_02286":null,"SJAG_02287":null,"SJAG_02294":null,"SJAG_02299":null,"SJAG_02300":null,"SJAG_02303":null,"SJAG_02311":null,"SJAG_02312":null,"SJAG_02314":null,"SJAG_02318":null,"SJAG_02319":null,"SJAG_02320":null,"SJAG_02324":null,"SJAG_02326":null,"SJAG_02329":null,"SJAG_02332":null,"SJAG_02335":null,"SJAG_02336":null,"SJAG_02340":null,"SJAG_02346":null,"SJAG_02347":null,"SJAG_02348":null,"SJAG_02359":null,"SJAG_02362":null,"SJAG_02368":null,"SJAG_02372":null,"SJAG_02373":null,"SJAG_02377":null,"SJAG_02378":null,"SJAG_02381":null,"SJAG_02382":null,"SJAG_02385":null,"SJAG_02392":null,"SJAG_02394":null,"SJAG_02396":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02416":null,"SJAG_02417":null,"SJAG_02419":null,"SJAG_02427":null,"SJAG_02431":null,"SJAG_02439":null,"SJAG_02444":null,"SJAG_02447":null,"SJAG_02451":null,"SJAG_02452":null,"SJAG_02458":null,"SJAG_02460":null,"SJAG_02464":null,"SJAG_02465":null,"SJAG_02466":null,"SJAG_02469":null,"SJAG_02472":null,"SJAG_02475":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02486":null,"SJAG_02487":null,"SJAG_02490":null,"SJAG_02499":null,"SJAG_02500":null,"SJAG_02506":null,"SJAG_02508":null,"SJAG_02509":null,"SJAG_02510":null,"SJAG_02511":null,"SJAG_02513":null,"SJAG_02514":null,"SJAG_02518":null,"SJAG_02521":null,"SJAG_02522":null,"SJAG_02527":null,"SJAG_02529":null,"SJAG_02530":null,"SJAG_02531":null,"SJAG_02535":null,"SJAG_02536":null,"SJAG_02540":null,"SJAG_02541":null,"SJAG_02542":null,"SJAG_02543":null,"SJAG_02544":null,"SJAG_02545":null,"SJAG_02546":null,"SJAG_02547":null,"SJAG_02549":null,"SJAG_02550":null,"SJAG_02553":null,"SJAG_02556":null,"SJAG_02560":null,"SJAG_02561":null,"SJAG_02563":null,"SJAG_02566":null,"SJAG_02571":null,"SJAG_02573":null,"SJAG_02575":null,"SJAG_02576":null,"SJAG_02585":null,"SJAG_02589":null,"SJAG_02592":null,"SJAG_02597":null,"SJAG_02600":null,"SJAG_02606":null,"SJAG_02607":null,"SJAG_02608":null,"SJAG_02609":null,"SJAG_02610":null,"SJAG_02611":null,"SJAG_02616":null,"SJAG_02621":null,"SJAG_02622":null,"SJAG_02624":null,"SJAG_02626":null,"SJAG_02627":null,"SJAG_02628":null,"SJAG_02629":null,"SJAG_02638":null,"SJAG_02643":null,"SJAG_02644":null,"SJAG_02645":null,"SJAG_02651":null,"SJAG_02652":null,"SJAG_02653":null,"SJAG_02659":null,"SJAG_02662":null,"SJAG_02663":null,"SJAG_02664":null,"SJAG_02667":null,"SJAG_02680":null,"SJAG_02681":null,"SJAG_02682":null,"SJAG_02690":null,"SJAG_02695":null,"SJAG_02697":null,"SJAG_02698":null,"SJAG_02700":null,"SJAG_02701":null,"SJAG_02702":null,"SJAG_02707":null,"SJAG_02708":null,"SJAG_02718":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02724":null,"SJAG_02725":null,"SJAG_02731":null,"SJAG_02736":null,"SJAG_02737":null,"SJAG_02747":null,"SJAG_02749":null,"SJAG_02754":null,"SJAG_02755":null,"SJAG_02758":null,"SJAG_02759":null,"SJAG_02761":null,"SJAG_02762":null,"SJAG_02768":null,"SJAG_02771":null,"SJAG_02773":null,"SJAG_02775":null,"SJAG_02777":null,"SJAG_02778":null,"SJAG_02790":null,"SJAG_02795":null,"SJAG_02798":null,"SJAG_02800":null,"SJAG_02802":null,"SJAG_02803":null,"SJAG_02807":null,"SJAG_02808":null,"SJAG_02810":null,"SJAG_02812":null,"SJAG_02813":null,"SJAG_02814":null,"SJAG_02818":null,"SJAG_02821":null,"SJAG_02828":null,"SJAG_02829":null,"SJAG_02830":null,"SJAG_02831":null,"SJAG_02835":null,"SJAG_02836":null,"SJAG_02838":null,"SJAG_02840":null,"SJAG_02846":null,"SJAG_02849":null,"SJAG_02861":null,"SJAG_02863":null,"SJAG_02864":null,"SJAG_02866":null,"SJAG_02869":null,"SJAG_02870":null,"SJAG_02871":null,"SJAG_02872":null,"SJAG_02873":null,"SJAG_02879":null,"SJAG_02886":null,"SJAG_02890":null,"SJAG_02891":null,"SJAG_02894":null,"SJAG_02899":null,"SJAG_02900":null,"SJAG_02904":null,"SJAG_02906":null,"SJAG_02907":null,"SJAG_02908":null,"SJAG_02911":null,"SJAG_02921":null,"SJAG_02922":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02927":null,"SJAG_02952":null,"SJAG_02980":null,"SJAG_02981":null,"SJAG_02990":null,"SJAG_02995":null,"SJAG_03006":null,"SJAG_03008":null,"SJAG_03011":null,"SJAG_03016":null,"SJAG_03020":null,"SJAG_03023":null,"SJAG_03025":null,"SJAG_03026":null,"SJAG_03028":null,"SJAG_03033":null,"SJAG_03034":null,"SJAG_03036":null,"SJAG_03040":null,"SJAG_03041":null,"SJAG_03042":null,"SJAG_03043":null,"SJAG_03044":null,"SJAG_03047":null,"SJAG_03048":null,"SJAG_03052":null,"SJAG_03053":null,"SJAG_03061":null,"SJAG_03062":null,"SJAG_03065":null,"SJAG_03067":null,"SJAG_03068":null,"SJAG_03070":null,"SJAG_03073":null,"SJAG_03077":null,"SJAG_03080":null,"SJAG_03086":null,"SJAG_03088":null,"SJAG_03092":null,"SJAG_03097":null,"SJAG_03113":null,"SJAG_03116":null,"SJAG_03119":null,"SJAG_03122":null,"SJAG_03126":null,"SJAG_03127":null,"SJAG_03128":null,"SJAG_03132":null,"SJAG_03133":null,"SJAG_03143":null,"SJAG_03144":null,"SJAG_03145":null,"SJAG_03146":null,"SJAG_03156":null,"SJAG_03157":null,"SJAG_03159":null,"SJAG_03161":null,"SJAG_03163":null,"SJAG_03164":null,"SJAG_03176":null,"SJAG_03179":null,"SJAG_03183":null,"SJAG_03192":null,"SJAG_03193":null,"SJAG_03197":null,"SJAG_03200":null,"SJAG_03214":null,"SJAG_03216":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03221":null,"SJAG_03230":null,"SJAG_03234":null,"SJAG_03235":null,"SJAG_03252":null,"SJAG_03254":null,"SJAG_03255":null,"SJAG_03259":null,"SJAG_03262":null,"SJAG_03264":null,"SJAG_03276":null,"SJAG_03277":null,"SJAG_03283":null,"SJAG_03284":null,"SJAG_03285":null,"SJAG_03286":null,"SJAG_03287":null,"SJAG_03289":null,"SJAG_03297":null,"SJAG_03298":null,"SJAG_03320":null,"SJAG_03326":null,"SJAG_03327":null,"SJAG_03335":null,"SJAG_03341":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03346":null,"SJAG_03350":null,"SJAG_03351":null,"SJAG_03353":null,"SJAG_03356":null,"SJAG_03357":null,"SJAG_03360":null,"SJAG_03364":null,"SJAG_03366":null,"SJAG_03374":null,"SJAG_03375":null,"SJAG_03376":null,"SJAG_03379":null,"SJAG_03380":null,"SJAG_03383":null,"SJAG_03387":null,"SJAG_03388":null,"SJAG_03402":null,"SJAG_03410":null,"SJAG_03411":null,"SJAG_03413":null,"SJAG_03418":null,"SJAG_03419":null,"SJAG_03421":null,"SJAG_03422":null,"SJAG_03423":null,"SJAG_03424":null,"SJAG_03425":null,"SJAG_03430":null,"SJAG_03431":null,"SJAG_03433":null,"SJAG_03436":null,"SJAG_03437":null,"SJAG_03438":null,"SJAG_03441":null,"SJAG_03444":null,"SJAG_03449":null,"SJAG_03451":null,"SJAG_03453":null,"SJAG_03454":null,"SJAG_03455":null,"SJAG_03458":null,"SJAG_03459":null,"SJAG_03460":null,"SJAG_03465":null,"SJAG_03466":null,"SJAG_03468":null,"SJAG_03471":null,"SJAG_03479":null,"SJAG_03484":null,"SJAG_03487":null,"SJAG_03491":null,"SJAG_03495":null,"SJAG_03498":null,"SJAG_03501":null,"SJAG_03508":null,"SJAG_03519":null,"SJAG_03525":null,"SJAG_03540":null,"SJAG_03542":null,"SJAG_03543":null,"SJAG_03544":null,"SJAG_03551":null,"SJAG_03554":null,"SJAG_03564":null,"SJAG_03567":null,"SJAG_03568":null,"SJAG_03569":null,"SJAG_03570":null,"SJAG_03576":null,"SJAG_03578":null,"SJAG_03579":null,"SJAG_03581":null,"SJAG_03583":null,"SJAG_03584":null,"SJAG_03592":null,"SJAG_03594":null,"SJAG_03596":null,"SJAG_03597":null,"SJAG_03599":null,"SJAG_03602":null,"SJAG_03603":null,"SJAG_03604":null,"SJAG_03609":null,"SJAG_03612":null,"SJAG_03615":null,"SJAG_03617":null,"SJAG_03619":null,"SJAG_03624":null,"SJAG_03625":null,"SJAG_03627":null,"SJAG_03628":null,"SJAG_03630":null,"SJAG_03631":null,"SJAG_03635":null,"SJAG_03636":null,"SJAG_03638":null,"SJAG_03646":null,"SJAG_03649":null,"SJAG_03654":null,"SJAG_03664":null,"SJAG_03666":null,"SJAG_03668":null,"SJAG_03673":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03682":null,"SJAG_03683":null,"SJAG_03685":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03694":null,"SJAG_03695":null,"SJAG_03696":null,"SJAG_03698":null,"SJAG_03699":null,"SJAG_03702":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03708":null,"SJAG_03713":null,"SJAG_03719":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03728":null,"SJAG_03730":null,"SJAG_03731":null,"SJAG_03745":null,"SJAG_03751":null,"SJAG_03752":null,"SJAG_03758":null,"SJAG_03762":null,"SJAG_03776":null,"SJAG_03780":null,"SJAG_03787":null,"SJAG_03789":null,"SJAG_03792":null,"SJAG_03794":null,"SJAG_03796":null,"SJAG_03810":null,"SJAG_03815":null,"SJAG_03832":null,"SJAG_03835":null,"SJAG_03839":null,"SJAG_03840":null,"SJAG_03843":null,"SJAG_03844":null,"SJAG_03846":null,"SJAG_03855":null,"SJAG_03859":null,"SJAG_03867":null,"SJAG_03872":null,"SJAG_03874":null,"SJAG_03876":null,"SJAG_03877":null,"SJAG_03884":null,"SJAG_03887":null,"SJAG_03888":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03901":null,"SJAG_03905":null,"SJAG_03906":null,"SJAG_03909":null,"SJAG_03911":null,"SJAG_03915":null,"SJAG_03916":null,"SJAG_03919":null,"SJAG_03921":null,"SJAG_03922":null,"SJAG_03923":null,"SJAG_03926":null,"SJAG_03927":null,"SJAG_03931":null,"SJAG_03936":null,"SJAG_03939":null,"SJAG_03941":null,"SJAG_03942":null,"SJAG_03944":null,"SJAG_03945":null,"SJAG_03952":null,"SJAG_03954":null,"SJAG_03956":null,"SJAG_03957":null,"SJAG_03967":null,"SJAG_03971":null,"SJAG_03981":null,"SJAG_03982":null,"SJAG_03984":null,"SJAG_03989":null,"SJAG_03997":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04005":null,"SJAG_04006":null,"SJAG_04010":null,"SJAG_04019":null,"SJAG_04020":null,"SJAG_04029":null,"SJAG_04030":null,"SJAG_04033":null,"SJAG_04036":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04040":null,"SJAG_04041":null,"SJAG_04052":null,"SJAG_04055":null,"SJAG_04056":null,"SJAG_04062":null,"SJAG_04066":null,"SJAG_04069":null,"SJAG_04074":null,"SJAG_04076":null,"SJAG_04077":null,"SJAG_04081":null,"SJAG_04083":null,"SJAG_04084":null,"SJAG_04088":null,"SJAG_04089":null,"SJAG_04092":null,"SJAG_04097":null,"SJAG_04100":null,"SJAG_04106":null,"SJAG_04108":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04126":null,"SJAG_04128":null,"SJAG_04140":null,"SJAG_04141":null,"SJAG_04142":null,"SJAG_04143":null,"SJAG_04150":null,"SJAG_04153":null,"SJAG_04160":null,"SJAG_04164":null,"SJAG_04168":null,"SJAG_04173":null,"SJAG_04174":null,"SJAG_04176":null,"SJAG_04177":null,"SJAG_04180":null,"SJAG_04183":null,"SJAG_04186":null,"SJAG_04187":null,"SJAG_04188":null,"SJAG_04190":null,"SJAG_04191":null,"SJAG_04194":null,"SJAG_04195":null,"SJAG_04201":null,"SJAG_04204":null,"SJAG_04205":null,"SJAG_04206":null,"SJAG_04207":null,"SJAG_04210":null,"SJAG_04213":null,"SJAG_04216":null,"SJAG_04224":null,"SJAG_04239":null,"SJAG_04244":null,"SJAG_04245":null,"SJAG_04252":null,"SJAG_04253":null,"SJAG_04255":null,"SJAG_04256":null,"SJAG_04257":null,"SJAG_04259":null,"SJAG_04261":null,"SJAG_04272":null,"SJAG_04274":null,"SJAG_04280":null,"SJAG_04281":null,"SJAG_04289":null,"SJAG_04293":null,"SJAG_04303":null,"SJAG_04304":null,"SJAG_04308":null,"SJAG_04310":null,"SJAG_04324":null,"SJAG_04330":null,"SJAG_04339":null,"SJAG_04341":null,"SJAG_04342":null,"SJAG_04346":null,"SJAG_04350":null,"SJAG_04355":null,"SJAG_04372":null,"SJAG_04375":null,"SJAG_04378":null,"SJAG_04381":null,"SJAG_04387":null,"SJAG_04388":null,"SJAG_04389":null,"SJAG_04395":null,"SJAG_04396":null,"SJAG_04400":null,"SJAG_04407":null,"SJAG_04412":null,"SJAG_04414":null,"SJAG_04424":null,"SJAG_04427":null,"SJAG_04436":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04461":null,"SJAG_04464":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04470":null,"SJAG_04475":null,"SJAG_04476":null,"SJAG_04477":null,"SJAG_04478":null,"SJAG_04479":null,"SJAG_04480":null,"SJAG_04490":null,"SJAG_04491":null,"SJAG_04492":null,"SJAG_04493":null,"SJAG_04494":null,"SJAG_04498":null,"SJAG_04508":null,"SJAG_04509":null,"SJAG_04512":null,"SJAG_04517":null,"SJAG_04524":null,"SJAG_04527":null,"SJAG_04530":null,"SJAG_04532":null,"SJAG_04534":null,"SJAG_04547":null,"SJAG_04551":null,"SJAG_04558":null,"SJAG_04561":null,"SJAG_04562":null,"SJAG_04566":null,"SJAG_04567":null,"SJAG_04574":null,"SJAG_04575":null,"SJAG_04576":null,"SJAG_04581":null,"SJAG_04582":null,"SJAG_04586":null,"SJAG_04595":null,"SJAG_04596":null,"SJAG_04597":null,"SJAG_04599":null,"SJAG_04601":null,"SJAG_04607":null,"SJAG_04609":null,"SJAG_04610":null,"SJAG_04613":null,"SJAG_04621":null,"SJAG_04623":null,"SJAG_04624":null,"SJAG_04626":null,"SJAG_04638":null,"SJAG_04640":null,"SJAG_04644":null,"SJAG_04650":null,"SJAG_04653":null,"SJAG_04654":null,"SJAG_04656":null,"SJAG_04663":null,"SJAG_04666":null,"SJAG_04669":null,"SJAG_04670":null,"SJAG_04671":null,"SJAG_04672":null,"SJAG_04680":null,"SJAG_04689":null,"SJAG_04692":null,"SJAG_04695":null,"SJAG_04696":null,"SJAG_04699":null,"SJAG_04700":null,"SJAG_04703":null,"SJAG_04712":null,"SJAG_04724":null,"SJAG_04744":null,"SJAG_04745":null,"SJAG_04746":null,"SJAG_04748":null,"SJAG_04753":null,"SJAG_04754":null,"SJAG_04755":null,"SJAG_04758":null,"SJAG_04766":null,"SJAG_04767":null,"SJAG_04768":null,"SJAG_04772":null,"SJAG_04781":null,"SJAG_04788":null,"SJAG_04791":null,"SJAG_04793":null,"SJAG_04813":null,"SJAG_04814":null,"SJAG_04815":null,"SJAG_04816":null,"SJAG_04817":null,"SJAG_04838":null,"SJAG_04839":null,"SJAG_04841":null,"SJAG_04847":null,"SJAG_04855":null,"SJAG_04863":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_04880":null,"SJAG_04884":null,"SJAG_04886":null,"SJAG_04887":null,"SJAG_04889":null,"SJAG_04893":null,"SJAG_04897":null,"SJAG_04901":null,"SJAG_04908":null,"SJAG_04911":null,"SJAG_04916":null,"SJAG_04917":null,"SJAG_04918":null,"SJAG_04919":null,"SJAG_04921":null,"SJAG_04929":null,"SJAG_04931":null,"SJAG_04932":null,"SJAG_04934":null,"SJAG_04936":null,"SJAG_04940":null,"SJAG_04943":null,"SJAG_04950":null,"SJAG_04973":null,"SJAG_04974":null,"SJAG_04977":null,"SJAG_04979":null,"SJAG_04980":null,"SJAG_04982":null,"SJAG_04989":null,"SJAG_04992":null,"SJAG_04993":null,"SJAG_04994":null,"SJAG_04995":null,"SJAG_04998":null,"SJAG_05001":null,"SJAG_05006":null,"SJAG_05010":null,"SJAG_05012":null,"SJAG_05019":null,"SJAG_05020":null,"SJAG_05105":null,"SJAG_05153":null,"SJAG_05173":null,"SJAG_05180":null,"SJAG_05185":null,"SJAG_05186":null,"SJAG_05187":null,"SJAG_05190":null,"SJAG_05192":null,"SJAG_05193":null,"SJAG_05196":null,"SJAG_05197":null,"SJAG_05205":null,"SJAG_05207":null,"SJAG_05216":null,"SJAG_05218":null,"SJAG_05220":null,"SJAG_05232":null,"SJAG_05237":null,"SJAG_05239":null,"SJAG_05244":null,"SJAG_05247":null,"SJAG_05248":null,"SJAG_05253":null,"SJAG_05260":null,"SJAG_05264":null,"SJAG_05265":null,"SJAG_05266":null,"SJAG_05270":null,"SJAG_05273":null,"SJAG_05276":null,"SJAG_05282":null,"SJAG_05285":null,"SJAG_05288":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05301":null,"SJAG_05307":null,"SJAG_05309":null,"SJAG_05313":null,"SJAG_05315":null,"SJAG_05319":null,"SJAG_05320":null,"SJAG_05321":null,"SJAG_05323":null,"SJAG_05329":null,"SJAG_05331":null,"SJAG_05333":null,"SJAG_05338":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_05573":null,"SJAG_05679":null,"SJAG_05694":null,"SJAG_05978":null,"SJAG_05979":null,"SJAG_06022":null,"SJAG_06110":null,"SJAG_06253":null,"SJAG_06270":null,"SJAG_06560":null,"SJAG_06597":null,"SJAG_06612":null,"SJAG_06613":null,"SJAG_06635":null,"SJAG_06642":null,"SJAG_07002":null,"SJAG_07009":null,"SJAG_07011":null,"SJAG_07013":null,"SJAG_07014":null,"SJAG_07018":null,"SJAG_16454":null,"SJAG_16455":null,"SJAG_16457":null,"SJAG_MIT05":null,"SJAG_MIT06":null,"SJAG_MIT07":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"intracellular membraneless organelle","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000044":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:21733045":null,"PMID:21802294":null,"PMID:23786411":null,"PMID:24184107":null,"PMID:25866389":null,"PMID:27059155":null,"PMID:27734801":null,"PMID:28655757":null,"PMID:30726171":null,"PMID:32109380":null,"PMID:32243490":null,"PMID:36148799":null},"synonyms":[{"name":"intracellular non-membrane-bounded organelle","type":"exact"},{"name":"intracellular non-membrane-enclosed organelle","type":"exact"}],"termid":"GO:0043232","terms_by_termid":{"GO:0000093":null,"GO:0000120":null,"GO:0000123":null,"GO:0000124":null,"GO:0000228":null,"GO:0000235":null,"GO:0000262":null,"GO:0000444":null,"GO:0000500":null,"GO:0000775":null,"GO:0000776":null,"GO:0000779":null,"GO:0000781":null,"GO:0000782":null,"GO:0000785":null,"GO:0000786":null,"GO:0000791":null,"GO:0000792":null,"GO:0000793":null,"GO:0000794":null,"GO:0000796":null,"GO:0000811":null,"GO:0000812":null,"GO:0000923":null,"GO:0000931":null,"GO:0000932":null,"GO:0000939":null,"GO:0000940":null,"GO:0001651":null,"GO:0001725":null,"GO:0005655":null,"GO:0005658":null,"GO:0005662":null,"GO:0005664":null,"GO:0005694":null,"GO:0005721":null,"GO:0005730":null,"GO:0005736":null,"GO:0005761":null,"GO:0005762":null,"GO:0005763":null,"GO:0005811":null,"GO:0005814":null,"GO:0005815":null,"GO:0005816":null,"GO:0005819":null,"GO:0005826":null,"GO:0005827":null,"GO:0005856":null,"GO:0005868":null,"GO:0005869":null,"GO:0005871":null,"GO:0005872":null,"GO:0005873":null,"GO:0005874":null,"GO:0005875":null,"GO:0005876":null,"GO:0005880":null,"GO:0005881":null,"GO:0005884":null,"GO:0005885":null,"GO:0005940":null,"GO:0008275":null,"GO:0008290":null,"GO:0008622":null,"GO:0010494":null,"GO:0015030":null,"GO:0015629":null,"GO:0015630":null,"GO:0016460":null,"GO:0016514":null,"GO:0016586":null,"GO:0016604":null,"GO:0016938":null,"GO:0022625":null,"GO:0022626":null,"GO:0022627":null,"GO:0030478":null,"GO:0030479":null,"GO:0030863":null,"GO:0030874":null,"GO:0030875":null,"GO:0030892":null,"GO:0030893":null,"GO:0030896":null,"GO:0030915":null,"GO:0030958":null,"GO:0030981":null,"GO:0030998":null,"GO:0031011":null,"GO:0031021":null,"GO:0031262":null,"GO:0031298":null,"GO:0031389":null,"GO:0031390":null,"GO:0031391":null,"GO:0031422":null,"GO:0031429":null,"GO:0031475":null,"GO:0031511":null,"GO:0031934":null,"GO:0032117":null,"GO:0032133":null,"GO:0032151":null,"GO:0032152":null,"GO:0032169":null,"GO:0032175":null,"GO:0032176":null,"GO:0032221":null,"GO:0032432":null,"GO:0032798":null,"GO:0033100":null,"GO:0033193":null,"GO:0033503":null,"GO:0033551":null,"GO:0033553":null,"GO:0033557":null,"GO:0033698":null,"GO:0034388":null,"GO:0034455":null,"GO:0034456":null,"GO:0034457":null,"GO:0034506":null,"GO:0034515":null,"GO:0034967":null,"GO:0034974":null,"GO:0035101":null,"GO:0035267":null,"GO:0035371":null,"GO:0035861":null,"GO:0035974":null,"GO:0036286":null,"GO:0036391":null,"GO:0036410":null,"GO:0036449":null,"GO:0042645":null,"GO:0042729":null,"GO:0043505":null,"GO:0043596":null,"GO:0043599":null,"GO:0043601":null,"GO:0043625":null,"GO:0044732":null,"GO:0045160":null,"GO:0046695":null,"GO:0055028":null,"GO:0055120":null,"GO:0061493":null,"GO:0061496":null,"GO:0061497":null,"GO:0061499":null,"GO:0061638":null,"GO:0061673":null,"GO:0061838":null,"GO:0062194":null,"GO:0070187":null,"GO:0070210":null,"GO:0070545":null,"GO:0070648":null,"GO:0070823":null,"GO:0070824":null,"GO:0070860":null,"GO:0071920":null,"GO:0071957":null,"GO:0071958":null,"GO:0072686":null,"GO:0072687":null,"GO:0090619":null,"GO:0097431":null,"GO:0099070":null,"GO:0099079":null,"GO:0099115":null,"GO:0110085":null,"GO:0120104":null,"GO:0120105":null,"GO:0120106":null,"GO:0140445":null,"GO:0140453":null,"GO:0140573":null,"GO:0140720":null,"GO:0160065":null,"GO:0180019":null,"GO:1903754":null,"GO:1904511":null,"GO:1905720":null,"GO:1905721":null,"GO:1905759":null,"GO:1905760":null,"GO:1990023":null,"GO:1990251":null,"GO:1990295":null,"GO:1990334":null,"GO:1990342":null,"GO:1990343":null,"GO:1990385":null,"GO:1990467":null,"GO:1990498":null,"GO:1990537":null,"GO:1990574":null,"GO:1990819":null,"GO:1990879":null,"GO:1990941":null}}


