# terms

id: PBO:0076346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin 13","termid":"PBO:0076346"}


id: PBO:0028714
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_rate_of_premeiotic_DNA_replication","termid":"PBO:0028714"}


id: GO:1903433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of constitutive secretory pathway.","definition_xrefs":["GOC:als","GOC:TermGenie","PMID:22899725","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of exocytosis","termid":"GO:0017157"},{"relation_name":"regulates","term_name":"constitutive secretory pathway","termid":"GO:0045054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"regulation of constitutive secretory pathway","termid":"GO:1903433"}


id: PBO:0041266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement C1q binding protein pseudogene 3","termid":"PBO:0041266"}


id: GO:0002844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of tolerance induction to tumor cell.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of peripheral tolerance induction","termid":"GO:0002659"},{"relation_name":"is_a","term_name":"negative regulation of immune response to tumor cell","termid":"GO:0002838"},{"relation_name":"is_a","term_name":"regulation of tolerance induction to tumor cell","termid":"GO:0002843"},{"relation_name":"negatively_regulates","term_name":"tolerance induction to tumor cell","termid":"GO:0002413"}],"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 tolerance induction to tumor cell","synonyms":[{"name":"down regulation of tolerance induction to tumor cell","type":"exact"},{"name":"down-regulation of tolerance induction to tumor cell","type":"exact"},{"name":"downregulation of tolerance induction to tumor cell","type":"exact"},{"name":"inhibition of tolerance induction to tumor cell","type":"narrow"},{"name":"negative regulation of tolerance induction to tumour cell","type":"exact"}],"termid":"GO:0002844"}


id: MONDO:0005898
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute or chronic infection of the soft tissues around the nail. Symptoms include pain, tenderness, erythema, and swelling around the nail. Acute infection results from minor trauma to the fingertip and Staphylococcus aureus is usually the causative agent. Chronic infection is usually caused by Candida albicans.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nail disorder","termid":"MONDO:0002884"},{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"paronychia","secondary_identifiers":["EFO:0007421","DOID:13117","ICD9:681.9","MEDGEN:45334","MESH:D010304","NCIT:C79702","UMLS:C0030578","HP:0001818","SCTID:71906005"],"synonyms":[{"name":"fungal nail infection","type":"exact"},{"name":"infected nailfold","type":"exact"},{"name":"onychia and paronychia of finger","type":"exact"},{"name":"onychia and paronychia of toe","type":"exact"},{"name":"paronychia","type":"exact"},{"name":"paronychia (disease)","type":"exact"},{"name":"paronychia inflammation","type":"related"}],"termid":"MONDO:0005898","xrefs":{"Monarch":{"xref_id":"0005898"}}}


id: PBO:0109257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 120 member A","termid":"PBO:0109257"}


id: PBO:0004555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNase P subunit Rpr2 (predicted)","termid":"PBO:0004555"}


id: PBO:0046728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"envoplakin","termid":"PBO:0046728"}


id: MONDO:0001015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Meningitis in which eosinophils predominate in the cerebrospinal fluid.","definition_xrefs":["NCIT:C128374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic meningitis","termid":"MONDO:0001007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eosinophilic meningitis","secondary_identifiers":["SCTID:25671008","DOID:10361","ICD9:322.1","MEDGEN:509620","UMLS:C0154652"],"termid":"MONDO:0001015","xrefs":{"Monarch":{"xref_id":"0001015"}}}


id: MONDO:0009923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare disorder of sex development (DSD) due to a defect in metabolizing testosterone to dihydrotestosterone and characterized by incomplete intrauterine masculinization which ranges from a female genitalia with a blind vaginal pouch to a fully male phenotype with pseudovaginal posterior hypospadias and micropenis.","definition_xrefs":["Orphanet:753"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency","secondary_identifiers":["GARD:5680","MESH:C535830","SCTID:57514000","MEDGEN:75667","NCIT:C98699","NANDO:2200389","OMIM:264600","icd11.foundation:1028755501","UMLS:C0268297","MedDRA:10000029"],"synonyms":[{"name":"3-oxo-5 Alpha-steroid Delta 4-dehydrogenase deficiency","type":"exact"},{"name":"46,XY DSD due to 5-alpha-reductase 2 deficiency","type":"exact"},{"name":"46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency","type":"exact"},{"name":"5 Alpha steroid reductase 2 deficiency","type":"exact"},{"name":"5-alpha reductase deficiency","type":"related"},{"name":"Male pseudohermaphroditism due to 5-Alpha-reductase deficiency","type":"related"},{"name":"Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency","type":"exact"},{"name":"PPSH","type":"related"},{"name":"familial incomplete Male pseudohermaphroditism, type 2","type":"related"},{"name":"micropenis","type":"related"},{"name":"pseudovaginal perineoscrotal hypospadias","type":"exact"},{"name":"steroid 5-alpha-reductase deficiency","type":"exact"}],"termid":"MONDO:0009923","xrefs":{"Monarch":{"xref_id":"0009923"}}}


id: MONDO:0025062
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A picornavirus infection producing symptoms similar to poliomyelitis in pigs.","definition_xrefs":["MESH:D004682"],"direct_ancestors":[{"relation_name":"is_a","term_name":"swine disease","termid":"MONDO:0024990"},{"relation_name":"is_a","term_name":"enterovirus infectious disease, non-human animal","termid":"MONDO:0700210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encephalomyelitis, enzootic porcine","synonyms":[{"name":"Talfan disease","type":"related"},{"name":"Teschen disease","type":"related"},{"name":"disease, Talfan","type":"related"},{"name":"disease, Teschen","type":"related"},{"name":"enzootic porcine encephalomyelitis","type":"related"},{"name":"poliomyelitis, porcine","type":"related"},{"name":"porcine encephalomyelitis, enzootic","type":"related"},{"name":"porcine poliomyelitis","type":"related"}],"termid":"MONDO:0025062","xrefs":{"Monarch":{"xref_id":"0025062"}}}


id: MONDO:0020390
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal origin of the pulmonary artery","termid":"MONDO:0015239"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary artery coming from patent ductus arteriosus","secondary_identifiers":["UMLS:C3163916","MEDGEN:756326","Orphanet:99049","GARD:19619"],"termid":"MONDO:0020390","xrefs":{"Monarch":{"xref_id":"0020390"}}}


id: PR:P87297
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dad1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87297"],"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":"DASH complex subunit dad1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16A10.05c","synonyms":[{"name":"Spom972h-dad1","type":"exact"},{"name":"outer kinetochore protein dad1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87297"}


id: PBO:0030868
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_actin_cytoskeleton_organization","termid":"PBO:0030868"}


id: FYPO:0001509
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during vegetative growth","termid":"FYPO:0000644"},{"relation_name":"is_a","term_name":"normal protein localization to chromatin","termid":"FYPO:0006163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0001312"],"is_obsolete":false,"name":"normal protein localization to chromatin during vegetative growth","synonyms":[{"name":"normal protein localisation to chromatin during vegetative growth","type":"exact"},{"name":"normal protein localization to chromatin during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001509"}


id: PBO:0000580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk14 (predicted)","termid":"PBO:0000580"}


id: GO:0006598
data:
  {"annotated_genes":["SJAG_03288"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009447"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of polyamines, any organic compound containing two or more amino groups.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine metabolic process","termid":"GO:0006595"},{"relation_name":"is_a","term_name":"biogenic amine catabolic process","termid":"GO:0042402"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03288":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"polyamine catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"polyamine breakdown","type":"exact"},{"name":"polyamine catabolism","type":"exact"},{"name":"polyamine degradation","type":"exact"}],"termid":"GO:0006598","terms_by_termid":{"GO:0009447":null}}


id: GO:0002830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of a type 2 immune response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of type 2 immune response","termid":"GO:0002828"},{"relation_name":"is_a","term_name":"positive regulation of immune response","termid":"GO:0050778"},{"relation_name":"positively_regulates","term_name":"type 2 immune response","termid":"GO:0042092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of type 2 immune response","synonyms":[{"name":"activation of type 2 immune response","type":"narrow"},{"name":"positive regulation of T-helper 2 type immune response","type":"narrow"},{"name":"positive regulation of Th2 immune response","type":"narrow"},{"name":"stimulation of type 2 immune response","type":"narrow"},{"name":"up regulation of type 2 immune response","type":"exact"},{"name":"up-regulation of type 2 immune response","type":"exact"},{"name":"upregulation of type 2 immune response","type":"exact"}],"termid":"GO:0002830"}


id: GO:0006620
data:
  {"annotated_genes":["SJAG_03396","SJAG_00175","SJAG_00959","SJAG_00064","SJAG_01496","SJAG_03955","SJAG_02354","SJAG_02330","SJAG_02588"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81203,97516,111161,111450],"is_not":false,"summary":null,"term":"GO:0006620"},{"annotations":[74847,99831,99114,110128,81943],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031204"}]},"cv_name":"biological_process","definition":"The targeting of proteins to a membrane that occurs after their translation. Some secretory proteins exhibit posttranslational transport into the endoplasmic reticulum (ER) lumen: they are synthesized in their entirety on free cytosolic ribosomes and then released into the cytosol, where they are bound by chaperones which keep them in an unfolded state, and subsequently are translocated across the ER membrane.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein targeting to membrane","termid":"GO:0006612"},{"relation_name":"is_a","term_name":"protein targeting to ER","termid":"GO:0045047"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00064":null,"SJAG_00175":null,"SJAG_00959":null,"SJAG_01496":null,"SJAG_02330":null,"SJAG_02354":null,"SJAG_02588":null,"SJAG_03396":null,"SJAG_03955":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006605","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"post-translational protein targeting to endoplasmic reticulum membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"SRP-independent endoplasmic reticulum protein-membrane targeting","type":"exact"},{"name":"posttranslational endoplasmic reticulum membrane targeting","type":"exact"},{"name":"posttranslational endoplasmic reticulum protein-membrane targeting","type":"exact"},{"name":"posttranslational protein endoplasmic reticulum membrane targeting","type":"exact"},{"name":"posttranslational protein targeting to ER membrane","type":"exact"},{"name":"posttranslational protein targeting to endoplasmic reticulum membrane","type":"exact"}],"termid":"GO:0006620","terms_by_termid":{"GO:0006620":null,"GO:0031204":null}}


id: PBO:0043238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride voltage-gated channel Kb","termid":"PBO:0043238"}


id: GO:0034070
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: acetyl-CoA + aminoglycoside = CoA + 1-N-acetylaminoglycoside. This is acetylation of the 1-amino group of the central deoxystreptamine ring.","definition_xrefs":["GOC:cb"],"gene_count":0,"genotype_count":0,"name":"obsolete aminoglycoside 1-N-acetyltransferase activity (obsolete GO:0034070)","termid":"GO:0034070"}


id: PBO:0048333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 44","termid":"PBO:0048333"}


id: PBO:0003108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L37a (predicted)","termid":"PBO:0003108"}


id: GO:0005127
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a ciliary neurotrophic factor receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor binding","termid":"GO:0005126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"ciliary neurotrophic factor receptor binding","synonyms":[{"name":"ciliary neurotrophic factor","type":"narrow"},{"name":"ciliary neurotrophic factor receptor ligand","type":"narrow"}],"termid":"GO:0005127"}


id: PBO:0040342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit f","termid":"PBO:0040342"}


id: PBO:0075291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNX30 divergent transcript","termid":"PBO:0075291"}


id: GO:0036356
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,3-diphosphoglycerate (DPG) + ATP = cyclic 2,3-diphosphoglycerate (cDPG) + ADP + phosphate.","definition_xrefs":["PMID:9811660","PMID:2226838","PMID:8320225","GOC:crds"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclase activity","termid":"GO:0009975"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0009975"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0009975","GO:0003674"],"is_obsolete":false,"name":"cyclic 2,3-diphosphoglycerate synthetase activity","synonyms":[{"name":"CPGS activity","type":"exact"},{"name":"cDPGS activity","type":"exact"}],"termid":"GO:0036356"}


id: MONDO:0008926
data:
  {"annotated_genes":["SJAG_00995","SJAG_02031","SJAG_02828","SJAG_04114"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008955"},{"annotations":[87418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012553"},{"annotations":[86731],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014696"},{"annotations":[87419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012554"},{"annotations":[88332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010216"}]},"cv_name":"mondo","definition":"Cerebrooculofacioskeletal (COFS) syndrome is a rare genetic disorder, belonging to a family of diseases of DNA repair, characterized by a severe sensorineural involvement.","definition_xrefs":["Orphanet:1466"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Cockayne syndrome","termid":"MONDO:0016006"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"syndromic microphthalmia","termid":"MONDO:0016073"},{"relation_name":"is_a","term_name":"DNA repair disease","termid":"MONDO:0021190"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00995":null,"SJAG_02031":null,"SJAG_02828":null,"SJAG_04114":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005066","MONDO:0021190","MONDO:0005328"],"is_obsolete":false,"name":"COFS syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NORD:913","UMLS:C5399761","MEDGEN:1762238","GARD:6027","OMIMPS:214150","DOID:0080910","NCIT:C3817"],"synonyms":[{"name":"COFS","type":"exact"},{"name":"Cerebro Oculo Facio Skeletal Syndrome","type":"exact"},{"name":"Pena-Shokeir syndrome type 2","type":"exact"},{"name":"cerebro-oculo-facio-skeletal syndrome","type":"exact"},{"name":"cerebrooculofacioskeletal syndrome","type":"exact"}],"termid":"MONDO:0008926","terms_by_termid":{"MONDO:0008955":null,"MONDO:0010216":null,"MONDO:0012553":null,"MONDO:0012554":null,"MONDO:0014696":null},"xrefs":{"Monarch":{"xref_id":"0008926"}}}


id: MONDO:0016501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hermansky-Pudlak syndrome with pulmonary fibrosis as a complication includes two types (HPS-1 and HPS-4) of Hermansky-Pudlak syndrome (HPS), a multi-system disorder characterized by oculocutaneous albinism, bleeding diathesis and, in some cases, pulmonary fibrosis or granulomatous colitis.","definition_xrefs":["Orphanet:231500"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interstitial lung disease specific to childhood","termid":"MONDO:0017014"},{"relation_name":"is_a","term_name":"Hermansky-Pudlak syndrome","termid":"MONDO:0019312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005570","MONDO:0005093"],"is_obsolete":false,"name":"Hermansky-Pudlak syndrome with pulmonary fibrosis","secondary_identifiers":["UMLS:C5679834","GARD:17168","MEDGEN:1843223","ICD10CM:E70.3","icd11.foundation:1086187623"],"synonyms":[{"name":"HPS with pulmonary fibrosis","type":"exact"}],"termid":"MONDO:0016501","xrefs":{"Monarch":{"xref_id":"0016501"}}}


id: PBO:0028449
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_meiotic_recombination_at_silent_mating-type_cassette","termid":"PBO:0028449"}


id: PR:P41838
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rae1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P41838"],"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":"poly(A)+ RNA export protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16A3.05c","synonyms":[{"name":"Spom972h-rae1","type":"exact"}],"termid":"PR:P41838"}


id: MONDO:0014285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital dyserythropoietic anemia type 1","termid":"MONDO:0020337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"congenital dyserythropoietic anemia type type 1B","secondary_identifiers":["OMIM:615631","UMLS:C3810185","GARD:15994","MEDGEN:816515","DOID:0111397"],"synonyms":[{"name":"CDA, type IB","type":"related"},{"name":"CDAN1B","type":"related"},{"name":"anemia, congenital dyserythropoietic, type IB","type":"exact"},{"name":"congenital dyserythropoietic anemia type type 1B","type":"exact"},{"name":"dyserythropoietic anemia, congenital, type IB","type":"exact"}],"termid":"MONDO:0014285","xrefs":{"Monarch":{"xref_id":"0014285"}}}


id: MONDO:0001272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"colonic disorder","termid":"MONDO:0003409"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"functional diarrhea","secondary_identifiers":["SCTID:47812002","MEDGEN:510199","UMLS:C0156173","ICD10CM:K59.1","DOID:11371","ICD9:564.5"],"termid":"MONDO:0001272","xrefs":{"Monarch":{"xref_id":"0001272"}}}


id: MONDO:0000798
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A allergic disease involving a mollusc food product.","definition_xrefs":["MONDO:patterns/allergy"],"gene_count":0,"genotype_count":0,"name":"obsolete mollusc allergy (obsolete MONDO:0000798)","secondary_identifiers":["DOID:0060523"],"synonyms":[{"name":"allergy of mollusc food product","type":"exact"},{"name":"mollusc food product allergic disease","type":"exact"}],"termid":"MONDO:0000798","xrefs":{"Monarch":{"xref_id":"0000798"}}}


id: GO:1904942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac ventricle formation.","definition_xrefs":["PMID:23575307","GO_REF:0000058","GOC:BHF_miRNA","GOC:bc","GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac chamber formation","termid":"GO:1901210"},{"relation_name":"regulates","term_name":"cardiac ventricle formation","termid":"GO:0003211"}],"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 ventricle formation","termid":"GO:1904942"}


id: GO:0043455
data:
  {"annotated_genes":["SJAG_00792"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95831],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905569"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of secondary metabolism, the chemical reactions and pathways involving compounds that are not necessarily required for growth and maintenance of cells, and are often unique to a taxon.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"secondary metabolic process","termid":"GO:0019748"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00792":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"regulation of secondary metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of secondary metabolism","type":"exact"}],"termid":"GO:0043455","terms_by_termid":{"GO:1905569":null}}


id: PBO:0043341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride nucleotide-sensitive channel 1A","termid":"PBO:0043341"}


id: MONDO:0010434
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Synovial sarcoma is an aggressive soft tissue sarcoma, occurring most commonly in adolescents and young adults (15 to 40 years), usually localized near the large joints of the extremities but also in the head and neck, mediastinum and viscera (lung, kidney etc), clinically presenting as a deep seated swelling or a painful mass often with an initial indolent course and is characterized by its local invasiveness and a propensity to metastasize. The origin of synovial sarcoma is likely from multipotent mesenchymal cells and not synovium (contrary to its name).","definition_xrefs":["Orphanet:3273"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"synovium cancer","termid":"MONDO:0002403"},{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"synovial sarcoma","secondary_identifiers":["NCIT:C3400","UMLS:C0039101","GARD:7721","EFO:0001376","ICD9:171.9","SCTID:302851001","ONCOTREE:SYNS","NANDO:2200061","HP:0012570","MedDRA:10042863","DOID:5485","OMIM:300813","ICDO:9040/3","MESH:D013584","MEDGEN:21050"],"synonyms":[{"name":"SS","type":"broad"},{"name":"Synovialosarcoma","type":"exact"},{"name":"sarcoma, synovial","type":"related"},{"name":"sarcoma, synovial, malignant","type":"exact"},{"name":"synovial sarcoma","type":"exact"},{"name":"synovial sarcoma (disease)","type":"exact"}],"termid":"MONDO:0010434","xrefs":{"Monarch":{"xref_id":"0010434"}}}


id: PBO:0000524
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STErile","termid":"PBO:0000524"}


id: GO:0097168
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of mesenchymal stem cells, resulting in the expansion of a stem cell population. A mesenchymal stem cell, or MSC, is a cell that retains the ability to divide and proliferate throughout life to provide progenitor cells that can differentiate into specialized mesenchymal cells.","definition_xrefs":["GOC:yaf","CL:0000134","PMID:20626275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stem cell proliferation","termid":"GO:0072089"}],"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":"mesenchymal stem cell proliferation","synonyms":[{"name":"MSC proliferation","type":"exact"}],"termid":"GO:0097168"}


id: PBO:0050189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosome binding domain 1 pseudogene 6","termid":"PBO:0050189"}


id: PBO:0036361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RhoGAP, GTPase activating protein Rga3","termid":"PBO:0036361"}


id: PBO:0004771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP complex subunit Trs23 (predicted)","termid":"PBO:0004771"}


id: MONDO:1012602
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lysosomal storage disease that occurs in dogs in which there is a buildup of GM2 gangliosides in tissues due to the lack of the enzyme hexosaminidase. It is characterised by progressive neuromuscular dysfunction and impaired growth from an early age.","definition_xrefs":["OMIA:000403-9615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gangliosidosis, dog","termid":"MONDO:1010840"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GM2 gangliosidosis, dog","synonyms":[{"name":"gangliosidosis, GM2, generic, dog","type":"related"}],"termid":"MONDO:1012602","xrefs":{"Monarch":{"xref_id":"1012602"}}}


id: PBO:0026746
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_polyubiquitination_during_cellular_response_to_UV","termid":"PBO:0026746"}


id: MONDO:1012268
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"androgen insensitivity syndrome, non-human animal","termid":"MONDO:1011919"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"androgen insensitivity syndrome, cattle","secondary_identifiers":["OMIA:000991-9913"],"synonyms":[{"name":"AIS, cattle","type":"exact"}],"termid":"MONDO:1012268","xrefs":{"Monarch":{"xref_id":"1012268"}}}


id: MONDO:0030036
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":"leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome","secondary_identifiers":["UMLS:C5394371","MEDGEN:1719764","OMIM:618878"],"synonyms":[{"name":"LEMSPAD","type":"exact"},{"name":"LEUKOENCEPHALOPATHY, MOTOR DELAY, SPASTICITY, AND DYSARTHRIA SYNDROME","type":"exact"},{"name":"Lemspad Syndrome","type":"exact"},{"name":"leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome","type":"exact"}],"termid":"MONDO:0030036","xrefs":{"Monarch":{"xref_id":"0030036"}}}


id: MONDO:1012310
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neuronal abiotrophy, non-human animal","termid":"MONDO:1011867"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal abiotrophy, dog","secondary_identifiers":["OMIA:001164-9615"],"termid":"MONDO:1012310","xrefs":{"Monarch":{"xref_id":"1012310"}}}


id: GO:0047818
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-fuconate = 2-dehydro-3-deoxy-D-fuconate + H2O.","definition_xrefs":["EC:4.2.1.67","RHEA:12949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"D-fuconate dehydratase activity","secondary_identifiers":["KEGG_REACTION:R03671","MetaCyc:D-FUCONATE-HYDRATASE-RXN"],"synonyms":[{"name":"D-fuconate hydratase activity","type":"exact"},{"name":"D-fuconate hydro-lyase (2-dehydro-3-deoxy-D-fuconate-forming)","type":"related"},{"name":"D-fuconate hydro-lyase activity","type":"related"}],"termid":"GO:0047818"}


id: PR:O14222
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fsv1 gene.","definition_xrefs":["UniProtKB:O14222","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":"syntaxin-like protein fsv1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F12.03c","synonyms":[{"name":"Spom972h-fsv1","type":"exact"}],"termid":"PR:O14222"}


id: PBO:0083998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), isozyme 3; involved in glycolysis and gluconeogenesis; tetramer that catalyzes the reaction of glyceraldehyde-3-phosphate to 1,3 bis-phosphoglycerate; detected in the cytoplasm and cell wall; GAPDH-derived antimicrobial peptides secreted by S. cerevisiae are active against a wide variety of wine-related yeasts and bacteria; binds AU-rich RNA","termid":"PBO:0083998"}


id: MONDO:0006133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare carcinoma that arises from the cervix. It is characterized by the presence of cystic spaces surrounded by palisaded epithelial cells. The cystic spaces contain eosinophilic hyaline material or mucin. Nuclear pleomorphism, necrotic changes, and a high mitotic rate are also present.","definition_xrefs":["NCIT:C6346"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenoid cystic carcinoma","termid":"MONDO:0004971"},{"relation_name":"is_a","term_name":"cervical adenocarcinoma","termid":"MONDO:0005153"}],"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":"cervical adenoid cystic carcinoma","secondary_identifiers":["GARD:20498","Orphanet:213823","UMLS:C1332911","EFO:1000161","ONCOTREE:CACC","ICD10CM:C53.0","MEDGEN:232337","DOID:4867"],"synonyms":[{"name":"adenoid cystic carcinoma of cervix","type":"exact"},{"name":"adenoid cystic carcinoma of cervix uteri","type":"exact"},{"name":"adenoid cystic carcinoma of the cervix","type":"exact"},{"name":"adenoid cystic carcinoma of the cervix uteri","type":"exact"},{"name":"adenoid cystic carcinoma of the uterine cervix","type":"exact"},{"name":"adenoid cystic carcinoma of uterine cervix","type":"exact"},{"name":"cervical adenoid cystic cancer","type":"exact"},{"name":"cervical adenoid cystic carcinoma","type":"exact"},{"name":"cervix uteri adenoid cystic carcinoma","type":"exact"},{"name":"uterine cervix adenoid cystic carcinoma","type":"exact"}],"termid":"MONDO:0006133","xrefs":{"Monarch":{"xref_id":"0006133"}}}


id: PBO:0042957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 11","termid":"PBO:0042957"}


id: MONDO:0001856
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"arterial disorder","termid":"MONDO:0000473"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splenic artery aneurysm","secondary_identifiers":["UMLS:C0155747","DOID:14006","ICD9:442.83","MEDGEN:510069","SCTID:70405009"],"termid":"MONDO:0001856","xrefs":{"Monarch":{"xref_id":"0001856"}}}


id: RO:0002342
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Holds between p and m when p is a transportation or localization process and the outcome of this process is to move c from one location to another, and the route taken by c follows a path that crosses m.","direct_ancestors":[{"relation_name":"is_a","term_name":"occurs_across","termid":"RO:0002021"},{"relation_name":"is_a","term_name":"results_in_transport_to_from_or_in","termid":"RO:0002344"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_transport_across","termid":"RO:0002342"}


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


id: PBO:0074301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLX1A-SULT1A3 readthrough (NMD candidate)","termid":"PBO:0074301"}


id: PBO:0116741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLIRP overlapping transcript 1","termid":"PBO:0116741"}


id: PBO:0044144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTBP2 pseudogene 10","termid":"PBO:0044144"}


id: MONDO:0016851
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome X disorder","termid":"MONDO:0700027"},{"relation_name":"is_a","term_name":"uniparental disomy","termid":"MONDO:0700086"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maternal uniparental disomy of chromosome X","secondary_identifiers":["icd11.foundation:573923144","MEDGEN:1673747","Orphanet:261519","GARD:20783","UMLS:C5191056"],"synonyms":[{"name":"UPD(X)mat","type":"exact"},{"name":"maternal uniparental disomy of chromosome type X","type":"exact"}],"termid":"MONDO:0016851","xrefs":{"Monarch":{"xref_id":"0016851"}}}


id: MONDO:0024280
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An arthritis affecting five or more separate joints.","definition_xrefs":["NCIT:C26996"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthritic joint disease","termid":"MONDO:0005578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyarticular arthritis","secondary_identifiers":["SCTID:416956002","UMLS:C0162323","MEDGEN:56408"],"synonyms":[{"name":"polyarthritis","type":"exact"},{"name":"polyarticular arthritis","type":"exact"}],"termid":"MONDO:0024280","xrefs":{"Monarch":{"xref_id":"0024280"}}}


id: PBO:0029948
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_tyrosine_phosphorylation_during_cellular_response_to_osmotic_stress","termid":"PBO:0029948"}


id: GO:0047156
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribose 5-phosphate + acetoin = 1-deoxy-D-altro-heptulose 7-phosphate + acetaldehyde.","definition_xrefs":["RHEA:21504"],"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:0016744"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016744","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"acetoin-ribose-5-phosphate transaldolase activity","secondary_identifiers":["EC:2.2.1.4","KEGG_REACTION:R02345","MetaCyc:2.2.1.4-RXN"],"synonyms":[{"name":"1-deoxy-D-altro-heptulose-7-phosphate synthase activity","type":"related"},{"name":"1-deoxy-D-altro-heptulose-7-phosphate synthetase activity","type":"related"},{"name":"3-hydroxybutan-2-one:D-ribose-5-phosphate aldehydetransferase activity","type":"related"},{"name":"3-hydroxybutan-3-one:D-ribose-5-phosphate aldehydetransferase activity","type":"related"}],"termid":"GO:0047156"}


id: FYECO:0000031
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which potassium ions were added to the assay buffer in excess compared to standard assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ ions","termid":"FYECO:0000030"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ K ions","synonyms":[{"name":"potassium ions added","type":"exact"}],"termid":"FYECO:0000031"}


id: PBO:0011502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexaprenyldihydroxybenzoate methyltransferase, Coq3 variant (predicted)","termid":"PBO:0011502"}


id: PBO:0084961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Myo-inositol transporter; member of the sugar transporter superfamily; expression is repressed by inositol and choline via Opi1p and derepressed via Ino2p and Ino4p; relative distribution to the vacuole increases upon DNA replication stress; ITR1 has a paralog, ITR2, that arose from the whole genome duplication","termid":"PBO:0084961"}


id: GO:0047249
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (25S)-5beta-spirostan-3beta-ol + UDP-D-glucose = (25S)-5beta-spirostan-3beta-yl beta-D-glucoside + H+ + UDP.","definition_xrefs":["EC:2.4.1.193","RHEA:14461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"sarsapogenin 3-beta-glucosyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.193-RXN","KEGG_REACTION:R04359"],"synonyms":[{"name":"UDP-glucose:(25S)-5beta-spirostan-3beta-ol 3-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:(25S)-5beta-spirostan-3beta-ol 3-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"sarsapogenin 3beta-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-sarsapogenin glucosyltransferase activity","type":"related"}],"termid":"GO:0047249"}


id: GO:0102893
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + betanidin = H+ + gomphrenin I + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete betanidin 6-O-glucosyltransferase activity (obsolete GO:0102893)","termid":"GO:0102893"}


id: PR:Q9UTN4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pfs2 gene.","definition_xrefs":["UniProtKB:Q9UTN4","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":"polyadenylation factor subunit 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC12G12.14c","synonyms":[{"name":"Spom972h-pfs2","type":"exact"}],"termid":"PR:Q9UTN4"}


id: MONDO:0013943
data:
  {"annotated_genes":["SJAG_03440"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88997],"is_not":false,"summary":null,"term":"MONDO:0013943"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"peroxisome biogenesis disorder","termid":"MONDO:0019234"},{"relation_name":"is_a","term_name":"peroxisome biogenesis disorder due to PEX16 defect","termid":"MONDO:0100269"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03440":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0019053","MONDO:0005244","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"peroxisome biogenesis disorder 8B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0081437","NCIT:C155763","OMIM:614877","MEDGEN:766874","UMLS:C3553960","GARD:15870"],"synonyms":[{"name":"PBD8B","type":"related"},{"name":"peroxisome biogenesis disorder 8B","type":"exact"},{"name":"peroxisome biogenesis disorder type 8B","type":"exact"}],"termid":"MONDO:0013943","terms_by_termid":{"MONDO:0013943":null},"xrefs":{"Monarch":{"xref_id":"0013943"}}}


id: GO:1905430
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 a glycine stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:18984164"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amino acid stimulus","termid":"GO:0071230"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to glycine","termid":"GO:1905429"}],"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 glycine","synonyms":[{"name":"cellular response to Gly","type":"exact"},{"name":"cellular response to aminoacetic acid","type":"exact"},{"name":"cellular response to aminoethanoic acid","type":"exact"},{"name":"cellular response to glycin","type":"exact"}],"termid":"GO:1905430"}


id: PBO:0002888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1770 family protein","termid":"PBO:0002888"}


id: PATO:0000796
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000796 regeneration value (obsolete PATO:0000796)","termid":"PATO:0000796"}


id: RO:0003302
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between an entity (e.g. a genotype, genetic variation, chemical, or environmental exposure) and a condition (a phenotype or disease), where the entity has some causal or contributing role that influences the condition.","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_related_to","termid":"RO:0002410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causes_or_contributes_to_condition","termid":"RO:0003302"}


id: FYPO:0007198
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cohesion between centromeres of sister chromatids is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","GO:0071962"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic sister chromatid cohesion","termid":"FYPO:0002390"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal mitotic centromeric sister chromatid cohesion","synonyms":[{"name":"normal centromeric sister chromatid cohesion during mitotic cell cycle","type":"related"},{"name":"normal mitotic centromeric sister chromatid cohesion during vegetative growth","type":"exact"},{"name":"normal mitotic chromosome cohesion at centromere","type":"exact"},{"name":"normal mitotic sister chromatid cohesion at centromere","type":"exact"},{"name":"normal sister chromatid cohesion at centromere during mitosis","type":"exact"}],"termid":"FYPO:0007198"}


id: PBO:0014615
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"antisense RNA complementary to adh1, minor transcript","termid":"PBO:0014615"}


id: MONDO:0021398
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polyp that involves the rectum.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rectal disorder","termid":"MONDO:0001593"},{"relation_name":"is_a","term_name":"polyp of large intestine","termid":"MONDO:0021392"}],"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":"polyp of rectum","secondary_identifiers":["NCIT:C3351","SCTID:39772007","ICD10CM:K62.1","MEDGEN:11150","UMLS:C0034887"],"synonyms":[{"name":"polyp of the rectum","type":"exact"},{"name":"rectal polyp","type":"exact"},{"name":"rectum polyp","type":"exact"}],"termid":"MONDO:0021398","xrefs":{"Monarch":{"xref_id":"0021398"}}}


id: MONDO:0100267
data:
  {"annotated_genes":["SJAG_02693"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013949"},{"annotations":[89004],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013950"}]},"cv_name":"mondo","definition":"Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX13 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_02693":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559","MONDO:0005066","MONDO:0019053","MONDO:0005244"],"is_obsolete":false,"name":"peroxisome biogenesis disorder due to PEX13 defect","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"PEX13 related Zellweger spectrum disorder","type":"exact"},{"name":"peroxisome biogenesis disorder due to PEX13 defect","type":"exact"}],"termid":"MONDO:0100267","terms_by_termid":{"MONDO:0013949":null,"MONDO:0013950":null},"xrefs":{"Monarch":{"xref_id":"0100267"}}}


id: PBO:0066568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhomboid like 1","termid":"PBO:0066568"}


id: MONDO:1011544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic pulmonary fibrosis that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic pulmonary fibrosis, non-human animal","termid":"MONDO:1011451"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic pulmonary fibrosis, domestic cat","secondary_identifiers":["OMIA:001417-9685"],"termid":"MONDO:1011544","xrefs":{"Monarch":{"xref_id":"1011544"}}}


id: MONDO:0850426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A B-cell lymphoma that is characterized by the abnormal rearrangement of two genes, MYC gene and either BCL2 or BCL6 genes.","definition_xrefs":["DOID:0081004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B-cell neoplasm","termid":"MONDO:0004095"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"high-grade B-cell lymphoma double-hit/triple-hit","termid":"MONDO:0850426","xrefs":{"Monarch":{"xref_id":"0850426"}}}


id: SO:0000402
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000402 enhancer_attribute (obsolete SO:0000402)","termid":"SO:0000402"}


id: GO:0033993
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a lipid stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to lipid","termid":"GO:0033993"}


id: PBO:0066002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RALGAPA1 pseudogene 1","termid":"PBO:0066002"}


id: MONDO:0859260
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":"Dworschak-Punetha neurodevelopmental syndrome","secondary_identifiers":["OMIM:619955","UMLS:C5677017","MEDGEN:1800957"],"termid":"MONDO:0859260","xrefs":{"Monarch":{"xref_id":"0859260"}}}


id: GO:2000883
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of starch catabolic process.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"regulation of starch catabolic process","termid":"GO:2000881"},{"relation_name":"is_a","term_name":"positive regulation of starch metabolic process","termid":"GO:2000906"},{"relation_name":"positively_regulates","term_name":"starch catabolic process","termid":"GO:0005983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"positive regulation of starch catabolic process","synonyms":[{"name":"positive regulation of starch breakdown","type":"exact"},{"name":"positive regulation of starch catabolism","type":"exact"},{"name":"positive regulation of starch degradation","type":"exact"}],"termid":"GO:2000883"}


id: FYPO:0000839
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell contains one nucleus, has no septum, is elongated, and is inviable. Progression through the mitotic cell cycle is arrested in all inviable elongated mononucleate aseptate cells.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"abnormally arrested mitotic cell cycle progression","termid":"FYPO:0000502"},{"relation_name":"is_a","term_name":"abnormally arrested mitotic cell cycle progression","termid":"FYPO:0000502"},{"relation_name":"is_a","term_name":"inviable elongated aseptate cell","termid":"FYPO:0002066"},{"relation_name":"is_a","term_name":"inviable aseptate mononucleate vegetative cell","termid":"FYPO:0003763"},{"relation_name":"is_a","term_name":"inviable elongated mononucleate vegetative cell","termid":"FYPO:0004255"},{"relation_name":"is_a","term_name":"elongated mononucleate aseptate vegetative cell","termid":"FYPO:0005773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000032"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000004","FYPO:0000032","FYPO:0000005","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"inviable elongated mononucleate aseptate cell","secondary_identifiers":["FYPO:0004923"],"synonyms":[{"name":"cell cycle-arrested elongated inviable mononucleate aseptate vegetative cell","type":"exact"},{"name":"elongated inviable mononucleate aseptate cell with mitotic cell cycle arrest during vegetative growth","type":"exact"},{"name":"elongated inviable mononucleate aseptate vegetative cell with cell cycle arrest","type":"exact"},{"name":"elongated mononucleate aseptate cell during vegetative growth","type":"exact"},{"name":"inviable elongated mononucleate aseptate cell during mitotic cell cycle","type":"related"},{"name":"inviable elongated mononucleate aseptate vegetative cell with arrested cell cycle","type":"exact"},{"name":"inviable elongated mononucleate aseptate vegetative cell with mitotic cell cycle arrest","type":"exact"},{"name":"lethal; elongated mononucleate aseptate cell","type":"exact"},{"name":"long aseptate mononucleate cell","type":"exact"},{"name":"mitotic cell cycle arrest with elongated inviable mononucleate aseptate cell","type":"exact"}],"termid":"FYPO:0000839"}


id: PBO:0111902
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SANT subfamily","termid":"PBO:0111902"}


id: PBO:0062863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OTU deubiquitinase, ubiquitin aldehyde binding 2","termid":"PBO:0062863"}


id: PBO:0113182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lipid-binding ER protein, enriched at nucleus-vacuolar junctions (NVJ); involved in nonvesicular transfer of ceramides from ER to Golgi during ER stress; may be involved in sterol metabolism or signaling at the NVJ; contains a synaptotagmin-like-mitochondrial-lipid binding protein (SMP) domain; binds phosphatidylinositols and other lipids in a large-scale study; may interact with ribosomes, based on co-purification experiments","termid":"PBO:0113182"}


id: MONDO:0032900
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 hypotonia and autistic features with or without hyperkinetic movements","secondary_identifiers":["MEDGEN:1684874","UMLS:C5231491","OMIM:618760"],"synonyms":[{"name":"NEDHAHM","type":"related"},{"name":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS","type":"related"}],"termid":"MONDO:0032900","xrefs":{"Monarch":{"xref_id":"0032900"}}}


id: MONDO:1012107
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hyperkinesis, non-human animal","termid":"MONDO:1011626"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperkinesis, dog","secondary_identifiers":["OMIA:000503-9615"],"termid":"MONDO:1012107","xrefs":{"Monarch":{"xref_id":"1012107"}}}


id: GO:0001561
data:
  {"annotated_genes":["SJAG_00706"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74919],"is_not":false,"summary":null,"term":"GO:0001561"}]},"cv_name":"biological_process","definition":"A metabolic pathway by which 3-methyl branched fatty acids are degraded. These compounds are not degraded by the normal peroxisomal beta-oxidation pathway, because the 3-methyl blocks the dehydrogenation of the hydroxyl group by hydroxyacyl-CoA dehydrogenase. The 3-methyl branched fatty acid is converted in several steps to pristenic acid, which can then feed into the beta-oxidative pathway.","definition_xrefs":["PMID:10198260"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid catabolic process","termid":"GO:0009062"},{"relation_name":"is_a","term_name":"fatty acid oxidation","termid":"GO:0019395"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00706":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"fatty acid alpha-oxidation","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:PWY-2501","Reactome:R-HSA-389599"],"termid":"GO:0001561","terms_by_termid":{"GO:0001561":null}}


id: PATO:0000787
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000787 neurobehavioral function value (obsolete PATO:0000787)","termid":"PATO:0000787"}


id: MONDO:0003592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant adipose tissue neoplasm of the stomach.","definition_xrefs":["NCIT:C5488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastric cancer","termid":"MONDO:0001056"},{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"gastric liposarcoma","secondary_identifiers":["DOID:5700","UMLS:C1333778","MEDGEN:272663"],"synonyms":[{"name":"gastric liposarcoma","type":"exact"},{"name":"liposarcoma of stomach","type":"exact"},{"name":"liposarcoma of the stomach","type":"exact"},{"name":"stomach liposarcoma","type":"exact"}],"termid":"MONDO:0003592","xrefs":{"Monarch":{"xref_id":"0003592"}}}


id: MONDO:0010538
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mononen-Karnes-Senac syndrome is characterized by skeletal dysplasia associated with finger malformations (brachydactyly with short and abducted thumbs, short index fingers, and markedly short and abducted great toes), variable mild short stature, and mild bowleg with overgrowth of the fibula. It has been described in two males, their mothers, and a maternal aunt. Females are less severely affected than males. X-linked dominant inheritance is suggested.","definition_xrefs":["Orphanet:2565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mononen-Karnes-Senac syndrome","secondary_identifiers":["MESH:C535914","OMIM:301940","SCTID:733095006","UMLS:C1844919","DOID:0110973","GARD:4886","MEDGEN:336815"],"synonyms":[{"name":"Mononen Karnes Senac syndrome","type":"related"},{"name":"Mononen type brachydactyly","type":"exact"},{"name":"brachydactyly Mononen type","type":"related"},{"name":"brachydactyly, Mononen type","type":"related"},{"name":"short and abducted thumbs and great toes","type":"exact"},{"name":"skeletal dysplasia brachydactyly","type":"related"},{"name":"skeletal dysplasia-brachydactyly syndrome","type":"exact"},{"name":"thumbs and great toes short and abducted","type":"related"},{"name":"thumbs and great toes, short and abducted","type":"related"}],"termid":"MONDO:0010538","xrefs":{"Monarch":{"xref_id":"0010538"}}}


id: PBO:0108838
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does not functionally complement S. japonicus mid1","termid":"PBO:0108838"}


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:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000294"],"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:0054624
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 2029","termid":"PBO:0054624"}


id: GO:0031247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly of actin rods, a cellular structure consisting of parallel, hexagonally arranged actin tubules.","definition_xrefs":["GOC:pg","PMID:14706699"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament bundle assembly","termid":"GO:0051017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0044085","GO:0030036"],"is_obsolete":false,"name":"actin rod assembly","synonyms":[{"name":"actin rod formation","type":"related"}],"termid":"GO:0031247"}


id: MOD:00235
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-nitrosyl-L-cysteine.","definition_xrefs":["PubMed:10442087","PubMed:11562475","PubMed:8637569","RESID:AA0230","Unimod:275","PubMed:15688001","PubMed:8626764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"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":"S-nitrosyl-L-cysteine","synonyms":[{"name":"(2R)-2-amino-3-nitrososulfanyl-propanoic acid","type":"exact"},{"name":"L-cysteine nitrite ester","type":"exact"},{"name":"MOD_RES S-nitrosocysteine","type":"exact"},{"name":"Nitrosyl","type":"related"},{"name":"S-nitrosocysteine","type":"exact"},{"name":"S-nitrosyl-L-cysteine","type":"exact"},{"name":"S-nitrosylation","type":"related"},{"name":"SNOCys","type":"exact"}],"termid":"MOD:00235"}


id: MONDO:0019645
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bilateral renal dysplasia is a form of renal dysplasia (RD), a renal tract malformation in which the development of both kidneys is abnormal and incomplete. Bilateral RD can be segmental, and of variable severity, with renal aplasia corresponding to extreme RD.","definition_xrefs":["Orphanet:93173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal dysplasia","termid":"MONDO:0019638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal dysplasia, bilateral","secondary_identifiers":["HP:0012582","MEDGEN:609101","GARD:19178","SCTID:204950001","UMLS:C0431698"],"synonyms":[{"name":"bilateral renal dysplasia","type":"exact"}],"termid":"MONDO:0019645","xrefs":{"Monarch":{"xref_id":"0019645"}}}


id: PBO:0074689
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 68B","termid":"PBO:0074689"}


id: PBO:0039413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase promoting complex subunit 16","termid":"PBO:0039413"}


id: FYPO:0004994
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the first meiotic nuclear division begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"delayed onset of meiosis","termid":"FYPO:0000477"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000631","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of meiosis I","synonyms":[{"name":"delayed meiosis I","type":"exact"},{"name":"delayed onset of first meiotic nuclear division","type":"exact"}],"termid":"FYPO:0004994"}


id: PBO:0113084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic ankyrin repeat-containing protein; co-purifies with Myo3p and Myo5p by large-scale affinity capture; localization of the long-tailed type I myosins is altered in the null mutant; N-terminally propionylated in vivo; contains three ankyrin repeats and an acidic tail; orthologous to human OSTF1","termid":"PBO:0113084"}


id: MONDO:0000301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An myiasis caused by infection with Oestrus ovis.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypodermyiasis","termid":"MONDO:0005805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"ophthalmomyiasis","secondary_identifiers":["DOID:0050268","MEDGEN:507965","SCTID:48216006","UMLS:C0027034"],"synonyms":[{"name":"Oestrus ovis caused myiasis","type":"exact"},{"name":"Oestrus ovis myiasis","type":"exact"},{"name":"ophthalmic myiasis","type":"exact"},{"name":"ophthalmomyiasis","type":"exact"}],"termid":"MONDO:0000301","xrefs":{"Monarch":{"xref_id":"0000301"}}}


id: GO:0002396
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form an MHC protein complex.","definition_xrefs":["PMID:15928678","ISBN:0781735149","PMID:15771591","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"MHC protein complex assembly","termid":"GO:0002396"}


id: PBO:0091076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uroporphyrinogen-III synthase Ups","termid":"PBO:0091076"}


id: GO:1900926
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of L-threonine import into cell.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amino acid import across plasma membrane","termid":"GO:0010958"},{"relation_name":"is_a","term_name":"regulation of organic acid transport","termid":"GO:0032890"},{"relation_name":"regulates","term_name":"L-threonine import across plasma membrane","termid":"GO:1903807"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"regulation of L-threonine import across plasma membrane","synonyms":[{"name":"regulation of L-threonine import","type":"broad"},{"name":"regulation of L-threonine uptake","type":"exact"}],"termid":"GO:1900926"}


id: PBO:0057845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3158-1","termid":"PBO:0057845"}


id: PBO:0072440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 4","termid":"PBO:0072440"}


id: GO:0071070
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha4-beta1 integrin complex bound to thrombospondin-2.","definition_xrefs":["PMID:11980922"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"alpha4-beta1 integrin-thrombospondin-2 complex","synonyms":[{"name":"ITGA4-ITGB1-THBS2 complex","type":"narrow"}],"termid":"GO:0071070"}


id: PBO:0034752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase complex ubiquitin-like protein ligase subunit Cti6","termid":"PBO:0034752"}


id: MONDO:0001084
data:
  {"annotated_genes":["SJAG_02848","SJAG_03588","SJAG_02384","SJAG_MIT13","SJAG_02007","SJAG_02641","SJAG_01179","SJAG_03972","SJAG_MIT03","SJAG_02656","SJAG_MIT15","SJAG_04376","SJAG_03957","SJAG_01816","SJAG_01630"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008134"},{"annotations":[87282,87283,87281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010788"},{"annotations":[87636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020737"},{"annotations":[88586],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015011"},{"annotations":[87123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033549"},{"annotations":[87512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008135"},{"annotations":[88002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957935"},{"annotations":[87797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957978"},{"annotations":[87200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008133"},{"annotations":[87408,87409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012543"},{"annotations":[87174,87173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014571"},{"annotations":[88371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007429"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"optic atrophy","termid":"MONDO:0003608"}],"gene_count":15,"genes_by_uniquename":{"SJAG_01179":null,"SJAG_01630":null,"SJAG_01816":null,"SJAG_02007":null,"SJAG_02384":null,"SJAG_02641":null,"SJAG_02656":null,"SJAG_02848":null,"SJAG_03588":null,"SJAG_03957":null,"SJAG_03972":null,"SJAG_04376":null,"SJAG_MIT03":null,"SJAG_MIT13":null,"SJAG_MIT15":null},"genotype_count":0,"is_obsolete":false,"name":"primary optic atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:377.11","SCTID:21098003","UMLS:C0155291","MEDGEN:509897","DOID:10627","ICD10CM:H47.21"],"termid":"MONDO:0001084","terms_by_termid":{"MONDO:0007429":null,"MONDO:0008133":null,"MONDO:0008134":null,"MONDO:0008135":null,"MONDO:0010788":null,"MONDO:0012543":null,"MONDO:0014571":null,"MONDO:0015011":null,"MONDO:0020737":null,"MONDO:0033549":null,"MONDO:0957935":null,"MONDO:0957978":null},"xrefs":{"Monarch":{"xref_id":"0001084"}}}


id: PBO:0074539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synuclein alpha interacting protein","termid":"PBO:0074539"}


id: MONDO:0015289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infectious epithelial keratitis is a rare, potentially sight-threatening, acquired ocular disease chracterized by corneal epithelium inflammation resulting from viral (mainly Herpes Simplex virus), bacterial, fungic or protist infection, manifesting with variable symptoms, such as conjunctival hyperemia, lacrimation, rapid onset of pain, blurred vision and/or photophobia, depending on the causative agent.","definition_xrefs":["Orphanet:137593"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"herpes simplex virus keratitis","termid":"MONDO:0015288"},{"relation_name":"is_a","term_name":"viral eye infection","termid":"MONDO:0020950"},{"relation_name":"is_a","term_name":"corneal infection","termid":"MONDO:0023865"}],"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":"infectious epithelial keratitis","secondary_identifiers":["icd11.foundation:2103923676","GARD:19877","UMLS:C4749790","MEDGEN:1660649"],"termid":"MONDO:0015289","xrefs":{"Monarch":{"xref_id":"0015289"}}}


id: PBO:0002767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PINT/PCI domain","termid":"PBO:0002767"}


id: PBO:0054053
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 1395","termid":"PBO:0054053"}


id: MONDO:0011600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital myasthenic syndrome characterized by postsynaptic neuromuscular junction defects, early-onset progressive muscle weakness, and prolonged opening and activity of the acetylcholine receptor channel that has material basis in heterozygous or rarely biallelic mutation in the CHRNE gene on chromosome 17p13.","definition_xrefs":["DOID:0110678","PMID:25792100","PMID:12141316","PMID:7531341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myasthenic syndrome 4","termid":"MONDO:1040021"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital myasthenic syndrome 4A","secondary_identifiers":["MEDGEN:908188","UMLS:C4225413","GARD:15387","OMIM:605809"],"synonyms":[{"name":"CMS Ia1","type":"exact"},{"name":"CMS1A1","type":"exact"},{"name":"CMS4A","type":"exact"},{"name":"Cms Ia1","type":"related"},{"name":"Cms Ia1, formerly","type":"related"},{"name":"congenital myasthenic syndrome 4A slow-channel","type":"exact"},{"name":"congenital myasthenic syndrome type 4A","type":"exact"},{"name":"congenital myasthenic syndrome type Ia1","type":"related"},{"name":"congenital myasthenic syndrome type Ia1, formerly","type":"related"},{"name":"congenital myasthenic syndrometype Ia1","type":"exact"},{"name":"myasthenic syndrome, congenital, 4A, slow-channel","type":"related"}],"termid":"MONDO:0011600","xrefs":{"Monarch":{"xref_id":"0011600"}}}


id: GO:0140021
data:
  {"annotated_genes":["SJAG_02050"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59112],"is_not":false,"summary":null,"term":"GO:0140021"}]},"cv_name":"biological_process","definition":"The process in which ADP is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:2541251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ADP transport","termid":"GO:0015866"},{"relation_name":"is_a","term_name":"purine-containing compound transmembrane transport","termid":"GO:0072530"},{"relation_name":"is_a","term_name":"nucleotide transmembrane transport","termid":"GO:1901679"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02050":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"mitochondrial ADP transmembrane transport","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:0140021","terms_by_termid":{"GO:0140021":null}}


id: PBO:0070878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15 pseudogene 9","termid":"PBO:0070878"}


id: MONDO:0005808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the conjunctiva in a newborn due to Chlamydia trachomatis which was acquired during labor and delivery.","definition_xrefs":["NCIT:C116817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chlamydia trachomatis infectious disease","termid":"MONDO:0005701"},{"relation_name":"is_a","term_name":"bacterial conjunctivitis","termid":"MONDO:0006668"}],"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":"inclusion conjunctivitis","secondary_identifiers":["SCTID:231861005","DOID:13800","EFO:0007324","ICD10CM:A74.0","ICD9:077.98","ICD9:077.0","MESH:D003235","UMLS:C0009770","MEDGEN:1095"],"synonyms":[{"name":"Chlamydial conjunctivitis","type":"exact"},{"name":"Paratrachoma","type":"related"},{"name":"Trachoma","type":"exact"},{"name":"adult inclusion conjunctivitis","type":"exact"},{"name":"inclusion blennorrhoea","type":"exact"},{"name":"inclusion blenorrhea","type":"exact"},{"name":"neonatal Chlamydia conjunctivitis","type":"exact"}],"termid":"MONDO:0005808","xrefs":{"Monarch":{"xref_id":"0005808"}}}


id: PBO:0031035
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitochondrion_organization","termid":"PBO:0031035"}


id: GO:0140083
data:
  {"annotated_genes":["SJAG_03780","SJAG_00475"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108764,114365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061995"}]},"cv_name":"molecular_function","definition":"Facilitating the removal of a protein or protein complex from a DNA molecule driven by ATP hydrolysis. This can be achieved for example by introducing non-canonical DNA structures or generating torque to directly inhibit a protein-DNA binding interaction.","definition_xrefs":["PMID:28552615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATP-dependent activity, acting on DNA","termid":"GO:0008094"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00475":null,"SJAG_03780":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:0140097"}],"interesting_parent_ids":["GO:0140097","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"ATP-dependent protein-DNA unloader activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"ATP-dependent protein-DNA unloading activity","type":"exact"},{"name":"protein-DNA unloading ATPase activity","type":"exact"}],"termid":"GO:0140083","terms_by_termid":{"GO:0061995":null}}


id: MONDO:0004348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal vascular disorder","termid":"MONDO:0002311"}],"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":"retinal telangiectasia","secondary_identifiers":["HP:0007763","SCTID:84884003","UMLS:C0154835","ICD9:362.15","MEDGEN:57598","DOID:7736"],"termid":"MONDO:0004348","xrefs":{"Monarch":{"xref_id":"0004348"}}}


id: MONDO:0007201
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Blepharophimosis, Ptosis, and Epicanthus Inversus syndrome (BPES) is an ophthalmic disorder characterized by blepharophimosis, ptosis, epicanthus inversus, and telecanthus, that can appear associated with (type I) or without premature ovarian failure (POF) (type II).","definition_xrefs":["Orphanet:126"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic developmental defect of the eye (obsolete MONDO:0015217)","termid":"MONDO:0015217"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"telecanthus","termid":"MONDO:0008537"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005047","MONDO:0000426"],"is_obsolete":false,"name":"blepharophimosis, ptosis, and epicanthus inversus syndrome","secondary_identifiers":["MESH:C562419","DOID:14778","OMIM:110100","GARD:23","MEDGEN:66312","NORD:862","SCTID:715391004","UMLS:C0220663"],"synonyms":[{"name":"BPES","type":"exact"},{"name":"BPES type 1","type":"related"},{"name":"BPES with Duane retraction syndrome","type":"related"},{"name":"BPES with ovarian failure","type":"related"},{"name":"BPES with premature ovarian failure","type":"related"},{"name":"BPES without ovarian failure","type":"related"},{"name":"BPES, type 1","type":"related"},{"name":"BPES, type 2","type":"related"},{"name":"BPES, type I, autosomal recessive","type":"related"},{"name":"Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome","type":"exact"},{"name":"blepharophimosis syndrome type 1","type":"related"},{"name":"blepharophimosis types 1 and 2","type":"exact"},{"name":"blepharophimosis, epicanthus inversus, and ptosis, type 1","type":"exact"},{"name":"blepharophimosis, epicanthus inversus, and ptosis, type 2","type":"exact"},{"name":"blepharophimosis, ptosis, and epicanthus inversus","type":"exact"},{"name":"blepharophimosis, ptosis, and epicanthus inversus syndrome","type":"exact"},{"name":"blepharophimosis, ptosis, and epicanthus inversus syndrome type 1","type":"related"},{"name":"blepharophimosis, ptosis, epicanthus inversus syndrome","type":"exact"},{"name":"blepharophimosis, ptosis, epicanthus inversus with ovarian failure","type":"related"},{"name":"blepharophimosis-epicanthus inversus-ptosis syndrome","type":"exact"}],"termid":"MONDO:0007201","xrefs":{"Monarch":{"xref_id":"0007201"}}}


id: PBO:0000654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCM binding protein homolog Mcb1 (predicted)","termid":"PBO:0000654"}


id: FYPO:0000903
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A microtubule cytoskeleton organization phenotype observed in the vegetative growth phase of the life cycle in which microtubule depolymerization, i.e. the removal of tubulin dimers from a microtubule, occurs at a lower rate, or speed, than normal.","definition_xrefs":["PomBase:mah","GO:0007019"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal rate of microtubule depolymerization during vegetative growth","termid":"FYPO:0007954"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000054","FYPO:0001320"],"is_obsolete":false,"name":"decreased rate of microtubule depolymerization during vegetative growth","synonyms":[{"name":"decreased microtubule depolymerization rate during vegetative growth","type":"exact"},{"name":"decreased rate of microtubule catastrophe during vegetative growth","type":"related"},{"name":"decreased rate of microtubule depolymerisation during vegetative growth","type":"exact"},{"name":"decreased rate of microtubule depolymerization during mitotic cell cycle","type":"related"},{"name":"decreased rate of microtubule shrinkage during vegetative growth","type":"related"},{"name":"increased microtubule stability during vegetative growth","type":"related"},{"name":"reduced rate of microtubule depolymerization during vegetative growth","type":"exact"}],"termid":"FYPO:0000903"}


id: MONDO:0971103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"Nicolau syndrome","secondary_identifiers":["MEDGEN:810780","Orphanet:664787","UMLS:C1142083"],"termid":"MONDO:0971103","xrefs":{"Monarch":{"xref_id":"0971103"}}}


id: GO:0039663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Merging of the virion membrane and a host membrane (host plasma membrane or host organelle membrane) that is involved in the uptake of a virus into a host cell.","definition_xrefs":["GOC:jl","UniProtKB-KW:KW-1168","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"}],"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":"membrane fusion involved in viral entry into host cell","synonyms":[{"name":"fusion of virus membrane with host membrane","type":"related"},{"name":"fusion of virus membrane with host membrane during viral entry","type":"related"},{"name":"viral entry into host cell via membrane fusion","type":"related"}],"termid":"GO:0039663"}


id: PBO:0072108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S13 pseudogene 6","termid":"PBO:0072108"}


id: SO:1000028
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosomal structure variation within a single chromosome.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"intrachromosomal","termid":"SO:0001510"},{"relation_name":"is_a","term_name":"chromosome_structure_variation","termid":"SO:1000183"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intrachromosomal_mutation","synonyms":[{"name":"intrachromosomal mutation","type":"exact"}],"termid":"SO:1000028"}


id: PBO:0035818
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_gene_conversion_during_vegetative_growth","termid":"PBO:0035818"}


id: GO:0075336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism stops, prevents, or reduces the frequency, rate or extent of its symbiont adenylate cyclase-mediated signal transduction as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of symbiont adenylate cyclase-mediated signal transduction in response to host (obsolete GO:0075336)","termid":"GO:0075336"}


id: PBO:0038965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activity dependent neuroprotector homeobox","termid":"PBO:0038965"}


id: PBO:0030660
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_Man9GlcNAc_level","termid":"PBO:0030660"}


id: GO:0016509
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a long-chain (3S)-3-hydroxy fatty acyl-CoA + NAD+ = a long-chain 3-oxo-fatty acyl-CoA + H+ + NADH. A long-chain fatty acid has an aliphatic tail containing 13 to 22 carbons.","definition_xrefs":["RHEA:52656"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3-hydroxyacyl-CoA dehydrogenase (NAD+) activity","termid":"GO:0003857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"long-chain-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity","secondary_identifiers":["EC:1.1.1.211","MetaCyc:1.1.1.211-RXN"],"synonyms":[{"name":"LCHAD","type":"related"},{"name":"beta-hydroxyacyl-CoA dehydrogenase activity","type":"related"},{"name":"long-chain 3-hydroxyacyl coenzyme A dehydrogenase activity","type":"related"},{"name":"long-chain-(S)-3-hydroxyacyl-CoA:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0016509"}


id: MONDO:0018268
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Medich giant platelet syndrome (MGPS) is a platelet granule disorder characterized by thrombocytopenia with giant platelets resulting in easy bleeding.","definition_xrefs":["Orphanet:370127"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha granule disease","termid":"MONDO:0020117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"Medich giant platelet syndrome","secondary_identifiers":["MEDGEN:931044","SCTID:718554005","GARD:21598","UMLS:C4305375"],"synonyms":[{"name":"Medich macrothrombocytopenia","type":"exact"}],"termid":"MONDO:0018268","xrefs":{"Monarch":{"xref_id":"0018268"}}}


id: MONDO:0017845
data:
  {"annotated_genes":["SJAG_00773","SJAG_01417","SJAG_16456","SJAG_00721","SJAG_01179","SJAG_00797"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958009"},{"annotations":[88491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012651"},{"annotations":[87225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012664"},{"annotations":[88823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013354"},{"annotations":[88414],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013776"},{"annotations":[87535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014803"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary ataxia","termid":"MONDO:0100309"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00721":null,"SJAG_00773":null,"SJAG_00797":null,"SJAG_01179":null,"SJAG_01417":null,"SJAG_16456":null},"genotype_count":0,"is_obsolete":false,"name":"spastic ataxia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:G11.4","DOID:0050952","OMIMPS:108600","GARD:21401","MEDGEN:376528","MESH:C564815","Orphanet:316226","UMLS:C1849156"],"synonyms":[{"name":"SPAX","type":"exact"}],"termid":"MONDO:0017845","terms_by_termid":{"MONDO:0012651":null,"MONDO:0012664":null,"MONDO:0013354":null,"MONDO:0013776":null,"MONDO:0014803":null,"MONDO:0958009":null},"xrefs":{"Monarch":{"xref_id":"0017845"}}}


id: PBO:0047726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibronectin 1","termid":"PBO:0047726"}


id: MONDO:0041850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial pneumonia","termid":"MONDO:0004652"},{"relation_name":"is_a","term_name":"gram-negative bacterial infections","termid":"MONDO:0021678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pneumonia caused by gram negative bacteria","secondary_identifiers":["UMLS:C0854248","SCTID:430395005","MEDGEN:678525"],"synonyms":[{"name":"gram negative pneumonia","type":"related"},{"name":"gramme negative pneumonia","type":"related"},{"name":"pneumonia caused by gram negative bacteria","type":"exact"},{"name":"pneumonia caused by gram-negative bacteria","type":"related"},{"name":"pneumonia due to gram negative bacteria","type":"exact"},{"name":"pneumonia due to gram-negative bacteria","type":"related"},{"name":"pneumonia due to gramme negative bacteria","type":"exact"}],"termid":"MONDO:0041850","xrefs":{"Monarch":{"xref_id":"0041850"}}}


id: SO:0005847
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is a member of a gene cassette, which is a mobile genetic element.","direct_ancestors":[{"relation_name":"is_a","term_name":"gene_cassette_member","termid":"SO:0005848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cassette_array_member","synonyms":[{"name":"cassette array member","type":"exact"}],"termid":"SO:0005847"}


id: PBO:0043606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen like tail subunit of asymmetric acetylcholinesterase","termid":"PBO:0043606"}


id: GO:0034346
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of type III interferon production. Interferon lambda is the only member of the type III interferon found so far.","definition_xrefs":["PMID:15546383","ISBN:0126896631","PMID:16734557","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytokine production","termid":"GO:0001819"},{"relation_name":"is_a","term_name":"regulation of type III interferon production","termid":"GO:0034344"},{"relation_name":"positively_regulates","term_name":"type III interferon production","termid":"GO:0034343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of type III interferon production","synonyms":[{"name":"activation of type III interferon production","type":"narrow"},{"name":"positive regulation of type III IFN production","type":"exact"},{"name":"stimulation of type III interferon production","type":"narrow"},{"name":"up regulation of type III interferon production","type":"exact"},{"name":"up-regulation of type III interferon production","type":"exact"},{"name":"upregulation of type III interferon production","type":"exact"}],"termid":"GO:0034346"}


id: MONDO:0012794
data:
  {"annotated_genes":["SJAG_02829"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88063],"is_not":false,"summary":null,"term":"MONDO:0012794"}]},"cv_name":"mondo","definition":"ANE syndrome is a rare, genetic, neuro-endocrino-cutaneous disorder characterized by highly variable degrees of alopecia, moderate to severe intellectual disability, progressive, late-onset motor deterioration and combined anterior pituitary hormone deficiency, manifesting with central hypogonadotropic hypogonadism, delayed or absent puberty, growth hormone deficiency (resulting in short stature), progressive central adrenal insufficiency and a hypoplastic anterior pituitary gland. Additional features include hypodontia, flexural reticulate hyperpigmentation, gynecomastia, microcephaly and kyphoscoliosis.","definition_xrefs":["Orphanet:157954"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital hypogonadotropic hypogonadism","termid":"MONDO:0015770"},{"relation_name":"is_a","term_name":"non-acquired combined pituitary hormone deficiency","termid":"MONDO:0018762"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02829":null},"genotype_count":0,"is_obsolete":false,"name":"ANE syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112244","UMLS:C2677535","MESH:C567425","OMIM:612079","MEDGEN:394313","GARD:16987"],"synonyms":[{"name":"ANE syndrome","type":"exact"},{"name":"alopecia, neurologic defects, and endocrinopathy syndrome","type":"related"},{"name":"alopecia-progressive neurological defect-endocrinopathy syndrome","type":"exact"},{"name":"anes","type":"related"}],"termid":"MONDO:0012794","terms_by_termid":{"MONDO:0012794":null},"xrefs":{"Monarch":{"xref_id":"0012794"}}}


id: GO:0071633
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: a dihydroceramide + H2O = a fatty acid + dihydrosphingosine.","definition_xrefs":["GOC:mah","PMID:10900202"],"gene_count":0,"genotype_count":0,"name":"obsolete dihydroceramidase activity (obsolete GO:0071633)","termid":"GO:0071633"}


id: GO:0061301
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the vasculature of the cerebellum is generated and organized.","definition_xrefs":["GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"cerebellum development","termid":"GO:0021549"},{"relation_name":"part_of","term_name":"cerebellum vasculature development","termid":"GO:0061300"}],"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":"cerebellum vasculature morphogenesis","termid":"GO:0061301"}


id: PBO:0039731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein C2","termid":"PBO:0039731"}


id: FYPO:0004992
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell during interphase of the meiotic cell cycle is lower than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during meiotic cell cycle","termid":"FYPO:0004991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein level during meiotic interphase","synonyms":[{"name":"decreased protein accumulation during meiotic interphase","type":"related"},{"name":"decreased protein level during interphase of meiotic cell cycle","type":"exact"},{"name":"reduced protein level during meiotic interphase","type":"exact"}],"termid":"FYPO:0004992"}


id: PBO:0086934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab family GTPase; involved in the exocytic pathway; mediates intra-Golgi traffic or the budding of post-Golgi vesicles from the trans-Golgi; YPT31 has a paralog, YPT32, that arose from the whole genome duplication; localizes to the transitional and late Golgi","termid":"PBO:0086934"}


id: MONDO:0013193
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any thyrotoxic periodic paralysis in which the cause of the disease is a mutation in the KCNJ18 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"thyrotoxic periodic paralysis","termid":"MONDO:0019201"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyrotoxic periodic paralysis, susceptibility to, 2","secondary_identifiers":["OMIM:613239","MEDGEN:413851","UMLS:C2750473"],"synonyms":[{"name":"KCNJ18 thyrotoxic periodic paralysis","type":"exact"},{"name":"TTPP2","type":"related"},{"name":"thyrotoxic periodic paralysis caused by mutation in KCNJ18","type":"exact"},{"name":"thyrotoxic periodic paralysis, susceptibility to, 2","type":"exact"},{"name":"thyrotoxic periodic paralysis, susceptibility to, type 2","type":"exact"}],"termid":"MONDO:0013193","xrefs":{"Monarch":{"xref_id":"0013193"}}}


id: PBO:0040560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-1,4-N-acetyl-galactosaminyltransferase 1","termid":"PBO:0040560"}


id: SO:1001260
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A Shine-Dalgarno sequence that stimulates recoding through interactions with the anti-Shine-Dalgarno in the RNA of small ribosomal subunits of translating ribosomes. The signal is only operative in Bacteria.","definition_xrefs":["SO:ke","PMID:12519954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"internal_ribosome_entry_site","termid":"SO:0000243"},{"relation_name":"is_a","term_name":"recoding_stimulatory_region","termid":"SO:1001268"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"internal_Shine_Dalgarno_sequence","synonyms":[{"name":"internal Shine Dalgarno sequence","type":"exact"},{"name":"internal Shine-Dalgarno sequence","type":"exact"}],"termid":"SO:1001260"}


id: GO:0102583
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cyanidin 3-O-beta-D-sambubioside + 4-coumaryl-CoA = cyanidin 3-O-[2''-O-xylosyl) 6''-O-(p-coumaroyl) glucoside + coenzyme A.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete cyanidin 3-O-glucoside-(2''-O-xyloside) 6''-O-acyltransferase activity (obsolete GO:0102583)","termid":"GO:0102583"}


id: PBO:0082929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic and mitochondrial alanyl-tRNA synthetase; required for protein synthesis; point mutation (cdc64-1 allele) causes cell cycle arrest at G1; lethality of null mutation is functionally complemented by human homolog AARS; mutations in human homolog AARS are associated with autoimmune disease polymyositis/dermatomyositis and with hereditary peripheral neuropathy, Charcot-Marie-Tooth (CMT) disease","termid":"PBO:0082929"}


id: PBO:0046170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELFN1 antisense RNA 1","termid":"PBO:0046170"}


id: PBO:0079276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription termination factor 2","termid":"PBO:0079276"}


id: PBO:0067148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 198, pseudogene","termid":"PBO:0067148"}


id: MONDO:0957247
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"congenital myopathy 22A, classic","secondary_identifiers":["OMIM:620351","UMLS:C5830453","DOID:0081354","MEDGEN:1841089"],"termid":"MONDO:0957247","xrefs":{"Monarch":{"xref_id":"0957247"}}}


id: PBO:0058109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4324","termid":"PBO:0058109"}


id: PBO:0068021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 326","termid":"PBO:0068021"}


id: GO:0102717
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: DIBOA-beta-D-glucoside + O2 + 2-oxoglutarate = TRIBOA-beta-D-glucoside + succinate + carbon dioxide.","definition_xrefs":["EC:1.14.11.59","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with 2-oxoglutarate as one donor, and the other dehydrogenated","termid":"GO:0050498"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"DIBOA-glucoside oxygenase activity","secondary_identifiers":["MetaCyc:RXN-6685","RHEA:32115"],"termid":"GO:0102717"}


id: PBO:0057581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 885","termid":"PBO:0057581"}


id: PBO:0027396
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_diacylglycerol_O-acyltransferase_activity","termid":"PBO:0027396"}


id: PBO:0050793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HTR3E antisense RNA 1","termid":"PBO:0050793"}


id: GO:0035506
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of myosin light chain kinase activity.","definition_xrefs":["GOC:bf","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of myosin light chain kinase activity (obsolete GO:0035506)","termid":"GO:0035506"}


id: GO:0035188
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The emergence of an immature organism from a protective structure.","definition_xrefs":["ISBN:0198612001","GOC:dgh","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organism emergence from protective structure","termid":"GO:0071684"},{"relation_name":"part_of","term_name":"multicellular organism development","termid":"GO:0007275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hatching","termid":"GO:0035188"}


id: PBO:0027094
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_rDNA_copy_number","termid":"PBO:0027094"}


id: PBO:0041357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement component 4 binding protein alpha","termid":"PBO:0041357"}


id: PR:Q9P7N4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tad3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7N4"],"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":"tRNA-specific adenosine deaminase subunit tad3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.04c","synonyms":[{"name":"Spom972h-tad3","type":"exact"},{"name":"tRNA-specific adenosine-34 deaminase subunit tad3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7N4"}


id: PBO:0070040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1337, pseudogene","termid":"PBO:0070040"}


id: PBO:0002613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cofactor for methionyl-and glutamyl-tRNA synthetases (predicted)","termid":"PBO:0002613"}


id: GO:0003284
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the septum primum over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrial septum development","termid":"GO:0003283"}],"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":"septum primum development","termid":"GO:0003284"}


id: PBO:0062971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A) binding protein cytoplasmic 3","termid":"PBO:0062971"}


id: GO:0004135
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1->6)-alpha-D-glucosidic branch linkages in glycogen phosphorylase limit dextrin. Limit dextrin is the highly branched core that remains after exhaustive treatment of glycogen with glycogen phosphorylase. It is formed because these enzymes cannot hydrolyze the (1->6) glycosidic linkages present.","definition_xrefs":["EC:3.2.1.33"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-glucosidase activity","termid":"GO:0090599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016798","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"amylo-alpha-1,6-glucosidase activity","secondary_identifiers":["MetaCyc:3.2.1.33-RXN","Reactome:R-HSA-71593"],"synonyms":[{"name":"amylo-1,6-glucosidase activity","type":"exact"},{"name":"amylopectin 1,6-glucosidase activity","type":"related"},{"name":"dextrin 6-alpha-D-glucosidase activity","type":"related"},{"name":"dextrin-1,6-glucosidase activity","type":"related"},{"name":"glycogen phosphorylase-limit dextrin alpha-1,6-glucohydrolase activity","type":"related"}],"termid":"GO:0004135"}


id: GO:1904857
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endothelial cell chemotaxis to vascular endothelial growth factor.","definition_xrefs":["PMID:21885851","GOC:BHF","GOC:BHF_miRNA","GOC:rph","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"is_a","term_name":"regulation of chemotaxis","termid":"GO:0050920"},{"relation_name":"is_a","term_name":"regulation of cellular response to vascular endothelial growth factor stimulus","termid":"GO:1902547"},{"relation_name":"regulates","term_name":"endothelial cell chemotaxis to vascular endothelial growth factor","termid":"GO:0090668"}],"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 endothelial cell chemotaxis to vascular endothelial growth factor","termid":"GO:1904857"}


id: PBO:0056843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B","termid":"PBO:0056843"}


id: PBO:0079925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"URB2 ribosome biogenesis homolog","termid":"PBO:0079925"}


id: MONDO:0007641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Futcher line (obsolete MONDO:0007641)","secondary_identifiers":["OMIM:137000"],"synonyms":[{"name":"Futcher line","type":"exact"},{"name":"Voigt lines","type":"exact"},{"name":"pigmentary demarcation lines","type":"exact"}],"termid":"MONDO:0007641","xrefs":{"Monarch":{"xref_id":"0007641"}}}


id: MONDO:0043291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An abnormality characterized by macroscopic or microscopic outpouchings of gallbladder mucosa into the muscle of the gallbladder wall. It may be associated with cholecystitis or gallstones.","definition_xrefs":["MESH:C535869"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"in situ carcinoma","termid":"MONDO:0004647"},{"relation_name":"is_a","term_name":"biliary tract disorder","termid":"MONDO:0004868"},{"relation_name":"is_a","term_name":"gallbladder disorder","termid":"MONDO:0005281"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"Rokitansky-Aschoff sinuses of the gallbladder","secondary_identifiers":["SCTID:22149007","MEDGEN:78636","UMLS:C0267892"],"synonyms":[{"name":"Aschoff-Rokitansky sinuses","type":"exact"},{"name":"Rokitansky-Aschoff sinuses","type":"related"},{"name":"intramural diverticulosis of the gallbladder","type":"related"}],"termid":"MONDO:0043291","xrefs":{"Monarch":{"xref_id":"0043291"}}}


id: MONDO:0004360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An osteosarcoma arising from the breast tissue.","definition_xrefs":["NCIT:C5189"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast sarcoma","termid":"MONDO:0002490"},{"relation_name":"is_a","term_name":"extraosseous osteosarcoma","termid":"MONDO:0002621"}],"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":"breast extraskeletal osteosarcoma","secondary_identifiers":["UMLS:C1335149","MEDGEN:235414","DOID:7787"],"synonyms":[{"name":"breast extraskeletal osteosarcoma","type":"exact"},{"name":"breast osteosarcoma","type":"exact"},{"name":"breast osteosarcoma (disease)","type":"exact"},{"name":"osteogenic breast sarcoma","type":"exact"},{"name":"osteogenic sarcoma of breast","type":"exact"},{"name":"osteogenic sarcoma of the breast","type":"exact"},{"name":"osteosarcoma of breast","type":"exact"},{"name":"osteosarcoma of the breast","type":"exact"}],"termid":"MONDO:0004360","xrefs":{"Monarch":{"xref_id":"0004360"}}}


id: GO:0030596
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of terminal non-reducing alpha-L-rhamnose residues in alpha-L-rhamnosides.","definition_xrefs":["EC:3.2.1.40"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"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:0016787","GO:0003674","GO:0003824","GO:0016798"],"is_obsolete":false,"name":"alpha-L-rhamnosidase activity","secondary_identifiers":["RHEA:17465","KEGG_REACTION:R02436","MetaCyc:3.2.1.40-RXN"],"synonyms":[{"name":"alpha-L-rhamnosidase N","type":"related"},{"name":"alpha-L-rhamnosidase T","type":"related"},{"name":"alpha-L-rhamnoside rhamnohydrolase activity","type":"related"}],"termid":"GO:0030596"}


id: PBO:0044759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 43","termid":"PBO:0044759"}


id: PBO:0084064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase-activating protein (RhoGAP) for Cdc42p and Rho5p; relocalizes from bud neck to cytoplasm upon DNA replication stress","termid":"PBO:0084064"}


id: GO:0045894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any mating-type specific process that stops, prevents or reduces the rate of cellular DNA-templated transcription.","definition_xrefs":["GOC:txnOH","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mating-type specific transcription, DNA-templated","termid":"GO:0007532"},{"relation_name":"is_a","term_name":"negative regulation of DNA-templated transcription","termid":"GO:0045892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006351"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006355","GO:0006351","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mating-type specific transcription, DNA-templated","synonyms":[{"name":"down regulation of transcription, mating-type specific","type":"exact"},{"name":"down-regulation of transcription, mating-type specific","type":"exact"},{"name":"downregulation of transcription, mating-type specific","type":"exact"},{"name":"inhibition of transcription, mating-type specific","type":"narrow"},{"name":"negative regulation of mating-type specific transcription, DNA-dependent","type":"exact"}],"termid":"GO:0045894"}


id: MONDO:0016481
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Silver-Russell syndrome","termid":"MONDO:0008394"},{"relation_name":"is_a","term_name":"partial duplication of the short arm of chromosome 11","termid":"MONDO:0016948"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"silver-Russell syndrome due to 11p15 microduplication","secondary_identifiers":["MEDGEN:1826103","Orphanet:231144","UMLS:C5680917","GARD:20605"],"termid":"MONDO:0016481","xrefs":{"Monarch":{"xref_id":"0016481"}}}


id: SO:0001557
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant which causes gain of polypeptide function with respect to a reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_function_variant","termid":"SO:0001554"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polypeptide_gain_of_function_variant","synonyms":[{"name":"polypeptide gain of function variant","type":"exact"}],"termid":"SO:0001557"}


id: PBO:0043276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 3 member A","termid":"PBO:0043276"}


id: GO:0001818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of production of a cytokine.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"is_a","term_name":"negative regulation of gene expression","termid":"GO:0010629"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cytokine production","secondary_identifiers":["GO:0042036","GO:0050710"],"synonyms":[{"name":"down regulation of cytokine biosynthetic process","type":"exact"},{"name":"down regulation of cytokine production","type":"exact"},{"name":"down-regulation of cytokine biosynthetic process","type":"exact"},{"name":"down-regulation of cytokine production","type":"exact"},{"name":"downregulation of cytokine biosynthetic process","type":"exact"},{"name":"downregulation of cytokine production","type":"exact"},{"name":"inhibition of cytokine biosynthetic process","type":"narrow"},{"name":"inhibition of cytokine production","type":"narrow"},{"name":"negative regulation of cytokine anabolism","type":"exact"},{"name":"negative regulation of cytokine biosynthesis","type":"exact"},{"name":"negative regulation of cytokine biosynthetic process","type":"narrow"},{"name":"negative regulation of cytokine formation","type":"exact"},{"name":"negative regulation of cytokine secretion","type":"narrow"},{"name":"negative regulation of cytokine synthesis","type":"exact"}],"termid":"GO:0001818"}


id: FYPO:0001435
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 erythromycin.","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:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002058","FYPO:0000139","FYPO:0000257","FYPO:0002060","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on erythromycin","synonyms":[{"name":"normal cell population growth in presence of erythromycin","type":"exact"},{"name":"normal cell population growth on erythromycin","type":"exact"},{"name":"normal cellular response to erythromycin","type":"related"},{"name":"normal vegetative cell population growth on erythromycin","type":"exact"}],"termid":"FYPO:0001435"}


id: GO:0044467
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of glial cell line-derived neurotrophic factor from a cell. Glial cell-derived neurotrophic factor (GDNF) is a small protein that potently promotes the survival of many types of neurons, notably dopaminergic and motor neurons.","definition_xrefs":["PMID:17505307","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"glial cell-derived neurotrophic factor production","synonyms":[{"name":"GDNF production","type":"exact"},{"name":"glial cell line-derived neurotrophic factor production","type":"related"},{"name":"glial cell-derived neurotrophic factor secretion","type":"narrow"}],"termid":"GO:0044467"}


id: GO:0031377
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A fatty acid synthase complex in which each polypeptide chain catalyzes a single activity, located in the mitochondrion.","definition_xrefs":["PMID:12957385","ISBN:0471331309","ISBN:0716720094","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial type II fatty acid synthase complex (obsolete GO:0031377)","synonyms":[{"name":"mitochondrial type II FAS complex","type":"exact"},{"name":"mitochondrial type II fatty acid synthase complex","type":"exact"}],"termid":"GO:0031377"}


id: PBO:0062473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily G member 1","termid":"PBO:0062473"}


id: MONDO:0011460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An arrhythmogenic right ventricular dysplasia associated with variation in the region 10p14-p12.","definition_xrefs":["PMID:10631146","DOID:0110075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated arrhythmogenic right ventricular dysplasia","termid":"MONDO:0016342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"arrhythmogenic right ventricular dysplasia 6","secondary_identifiers":["MEDGEN:346892","MESH:C565775","UMLS:C1858378","OMIM:604401"],"synonyms":[{"name":"ARVC6","type":"exact"},{"name":"ARVD6","type":"exact"},{"name":"arrhythmogenic right ventricular cardiomyopathy 6","type":"exact"},{"name":"arrhythmogenic right ventricular dysplasia type 6","type":"exact"},{"name":"arrhythmogenic right ventricular dysplasia, familial, 6","type":"related"},{"name":"familial arrhythmogenic right ventricular dysplasia 6","type":"exact"}],"termid":"MONDO:0011460","xrefs":{"Monarch":{"xref_id":"0011460"}}}


id: PBO:0052302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH-type splicing regulatory protein","termid":"PBO:0052302"}


id: GO:0030835
data:
  {"annotated_genes":["SJAG_01993","SJAG_01894","SJAG_02700","SJAG_00279"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81888,80835,77228,94097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of actin depolymerization.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament depolymerization","termid":"GO:0030834"},{"relation_name":"is_a","term_name":"negative regulation of cytoskeleton organization","termid":"GO:0051494"},{"relation_name":"is_a","term_name":"negative regulation of protein depolymerization","termid":"GO:1901880"},{"relation_name":"is_a","term_name":"negative regulation of supramolecular fiber organization","termid":"GO:1902904"},{"relation_name":"negatively_regulates","term_name":"actin filament depolymerization","termid":"GO:0030042"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00279":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02700":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0030036"],"is_obsolete":false,"name":"negative regulation of actin filament depolymerization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0030044"],"synonyms":[{"name":"actin filament stabilization","type":"exact"},{"name":"down regulation of actin filament depolymerization","type":"exact"},{"name":"down-regulation of actin filament depolymerization","type":"exact"},{"name":"downregulation of actin filament depolymerization","type":"exact"},{"name":"inhibition of actin filament depolymerization","type":"narrow"},{"name":"negative regulation of actin depolymerization","type":"exact"},{"name":"negative regulation of actin polymerization and/or depolymerization","type":"broad"}],"termid":"GO:0030835","terms_by_termid":{"GO:0051016":null}}


id: GO:0071611
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of granulocyte colony-stimulating factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:rv","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"granulocyte colony-stimulating factor production","synonyms":[{"name":"CSF3 production","type":"exact"},{"name":"G-CSF production","type":"exact"},{"name":"colony stimulating factor 3 (granulocyte) production","type":"exact"},{"name":"filgrastim production","type":"exact"},{"name":"granulocyte colony stimulating factor production","type":"exact"},{"name":"lenograstim production","type":"exact"},{"name":"pluripoietin production","type":"exact"}],"termid":"GO:0071611"}


id: MONDO:0004264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute endometritis","termid":"MONDO:0004265"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute gonococcal endometritis","secondary_identifiers":["SCTID:65295003","DOID:7527","UMLS:C0153196","MEDGEN:509198","ICD9:098.16"],"synonyms":[{"name":"acute gonorrhea of uterus","type":"exact"},{"name":"acute gonorrhoea of uterus","type":"exact"},{"name":"gonococcal endometritis","type":"exact"},{"name":"gonococcal endometritis (acute)","type":"exact"},{"name":"uterus - acute gonorrhea","type":"exact"},{"name":"uterus - acute gonorrhoea","type":"exact"}],"termid":"MONDO:0004264","xrefs":{"Monarch":{"xref_id":"0004264"}}}


id: MONDO:0054813
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Ehlers-Danlos syndrome, classic-like, 2","secondary_identifiers":["OMIM:618000","UMLS:C4693870","GARD:17975","Orphanet:536532","DOID:0080732","MEDGEN:1632001"],"synonyms":[{"name":"EDSCLL2","type":"exact"},{"name":"Ehlers-Danlos syndrome, classic-like, 2","type":"exact"}],"termid":"MONDO:0054813","xrefs":{"Monarch":{"xref_id":"0054813"}}}


id: PBO:0016105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamine-dependent NAD(+) synthetase Qns1 (predicted)","termid":"PBO:0016105"}


id: PBO:0067532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 676, pseudogene","termid":"PBO:0067532"}


id: GO:1903568
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein localization to ciliary membrane.","definition_xrefs":["GO_REF:0000058","GOC:krc","GOC:TermGenie","GOC:cilia","PMID:22072986"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein localization to cilium","termid":"GO:1903565"},{"relation_name":"is_a","term_name":"regulation of protein localization to ciliary membrane","termid":"GO:1903567"},{"relation_name":"is_a","term_name":"negative regulation of protein localization to cell periphery","termid":"GO:1904376"},{"relation_name":"is_a","term_name":"negative regulation of protein localization to membrane","termid":"GO:1905476"},{"relation_name":"negatively_regulates","term_name":"protein localization to ciliary membrane","termid":"GO:1903441"}],"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 protein localization to ciliary membrane","synonyms":[{"name":"down regulation of protein localisation in ciliary membrane","type":"exact"},{"name":"down regulation of protein localisation to ciliary membrane","type":"exact"},{"name":"down regulation of protein localization in ciliary membrane","type":"exact"},{"name":"down regulation of protein localization to ciliary membrane","type":"exact"},{"name":"down-regulation of protein localisation in ciliary membrane","type":"exact"},{"name":"down-regulation of protein localisation to ciliary membrane","type":"exact"},{"name":"down-regulation of protein localization in ciliary membrane","type":"exact"},{"name":"down-regulation of protein localization to ciliary membrane","type":"exact"},{"name":"downregulation of protein localisation in ciliary membrane","type":"exact"},{"name":"downregulation of protein localisation to ciliary membrane","type":"exact"},{"name":"downregulation of protein localization in ciliary membrane","type":"exact"},{"name":"downregulation of protein localization to ciliary membrane","type":"exact"},{"name":"inhibition of protein localisation in ciliary membrane","type":"narrow"},{"name":"inhibition of protein localisation to ciliary membrane","type":"narrow"},{"name":"inhibition of protein localization in ciliary membrane","type":"narrow"},{"name":"inhibition of protein localization to ciliary membrane","type":"narrow"},{"name":"negative regulation of protein localisation in ciliary membrane","type":"exact"},{"name":"negative regulation of protein localisation to ciliary membrane","type":"exact"},{"name":"negative regulation of protein localization in ciliary membrane","type":"exact"}],"termid":"GO:1903568"}


id: GO:0015928
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of fucosyl compounds, substances containing a group derived from a cyclic form of fucose or a fucose derivative.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016798"],"is_obsolete":false,"name":"fucosidase activity","termid":"GO:0015928"}


id: MONDO:0008397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aplasia of the lacrimal and salivary glands (ALSG) is a rare autosomal dominant disorder characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary glands leading to varying features since infancy such as recurrent eye infections, irritable eyes, epiphora, xerostomia, dental caries, dental erosion and oral inflammation.","definition_xrefs":["Orphanet:86815"],"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":"aplasia of lacrimal and salivary glands","secondary_identifiers":["GARD:16759","icd11.foundation:539255304","OMIM:180920","DOID:0111549","SCTID:715656004","UMLS:C0158667","MEDGEN:57641"],"synonyms":[{"name":"ALSG","type":"exact"},{"name":"aplasia of lacrimal and salivary glands","type":"exact"},{"name":"congenital absence of lacrimal puncta and salivary glands","type":"exact"},{"name":"parotid aplasia or hypoplasia","type":"related"},{"name":"salivary glands, absence of","type":"related"},{"name":"salivary glands, absence of, include","type":"related"}],"termid":"MONDO:0008397","xrefs":{"Monarch":{"xref_id":"0008397"}}}


id: PR:O74436
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A signal recognition particle subunit SRP68 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04287","PANTHER:PTHR12860:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal recognition particle subunit srp68 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1682.05c","secondary_identifiers":["UniProtKB:O74436"],"synonyms":[{"name":"Spom972h-SRP68","type":"exact"},{"name":"signal recognition particle 68 kDa protein homolog (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74436"}


id: PBO:0002213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane amino acid permease Per1","termid":"PBO:0002213"}


id: MONDO:0000818
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lethal congenital contracture syndrome 4 (obsolete MONDO:0000818)","termid":"MONDO:0000818","xrefs":{"Monarch":{"xref_id":"0000818"}}}


id: GO:0045239
data:
  {"annotated_genes":["SJAG_03163","SJAG_06382","SJAG_01524","SJAG_03290","SJAG_02464","SJAG_03813"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[71909,73436,108547,65112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045252"},{"annotations":[77015,116812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009361"}]},"cv_name":"cellular_component","definition":"Any of the heteromeric enzymes that act in the TCA cycle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01524":null,"SJAG_02464":null,"SJAG_03163":null,"SJAG_03290":null,"SJAG_03813":null,"SJAG_06382":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:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"tricarboxylic acid cycle heteromeric enzyme complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"TCA cycle enzyme complex","type":"exact"}],"termid":"GO:0045239","terms_by_termid":{"GO:0009361":null,"GO:0045252":null}}


id: GO:0060332
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of a response to type II interferon (interferon-gamma). Response to interferon gamma is a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interferon-gamma stimulus.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of innate immune response","termid":"GO:0045089"},{"relation_name":"is_a","term_name":"regulation of response to type II interferon","termid":"GO:0060330"},{"relation_name":"is_a","term_name":"positive regulation of response to cytokine stimulus","termid":"GO:0060760"},{"relation_name":"positively_regulates","term_name":"response to type II interferon","termid":"GO:0034341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of response to type II interferon","synonyms":[{"name":"positive regulation of response to gamma-interferon","type":"related"},{"name":"positive regulation of response to immune interferon","type":"exact"},{"name":"positive regulation of response to interferon-gamma","type":"exact"},{"name":"positive regulation of response to type II IFN","type":"broad"}],"termid":"GO:0060332"}


id: PBO:0017427
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-integral_part_of","termid":"PBO:0017427"}


id: GO:0014906
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a myotube cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell. This occurs as part of the process of skeletal muscle regeneration. Myotubes are multinucleated cells that are formed when proliferating myoblasts exit the cell cycle, differentiate and fuse.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myotube cell development","termid":"GO:0014904"},{"relation_name":"part_of","term_name":"myotube differentiation involved in skeletal muscle regeneration","termid":"GO:0014908"}],"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":"myotube cell development involved in skeletal muscle regeneration","termid":"GO:0014906"}


id: MONDO:1010571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes mellitus that occurs in domestic guinea pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetes mellitus, non-human animal","termid":"MONDO:1010052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetes mellitus, domestic guinea pig","secondary_identifiers":["OMIA:000279-10141"],"termid":"MONDO:1010571","xrefs":{"Monarch":{"xref_id":"1010571"}}}


id: MOD:01077
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:216"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ethanedithiol/TFA cyclic adduct","termid":"MOD:01077"}


id: PATO:0001243
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of blue hue and high brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blue","termid":"PATO:0000318"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"light blue","termid":"PATO:0001243"}


id: GO:1904866
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a ventral tegmental area (VTA) over time, from its formation to the mature structure.","definition_xrefs":["GOC:PARL","PMID:26548362","GO_REF:0000094","GOC:TermGenie","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"midbrain development","termid":"GO:0030901"}],"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":"ventral tegmental area development","synonyms":[{"name":"VTA development","type":"broad"},{"name":"a10a development","type":"exact"},{"name":"area tegmentalis ventralis (Tsai) development","type":"related"},{"name":"area tegmentalis ventralis development","type":"related"},{"name":"tegmentum ventrale development","type":"related"},{"name":"ventral brain stem development","type":"related"},{"name":"ventral tegmental area (Tsai) development","type":"related"},{"name":"ventral tegmental area of tsai development","type":"exact"},{"name":"ventral tegmental nucleus (Rioch) development","type":"related"},{"name":"ventral tegmental nucleus (tsai) development","type":"exact"},{"name":"ventral tegmental nucleus of tsai development","type":"exact"},{"name":"ventral tegmentum development","type":"exact"},{"name":"ventromedial mesencephalic tegmentum development","type":"related"}],"termid":"GO:1904866"}


id: PR:Q9P7L3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC21C3.10c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7L3"],"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":"2,5-diamino-6-ribosylamino-4(3H)-pyrimidinone 5'-phosphate reductase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21C3.10c","synonyms":[{"name":"2,5-diamino-6-(5-phospho-D-ribosylamino)pyrimidin-4(3H)-one reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"2,5-diamino-6-ribitylamino-4(3H)-pyrimidinone 5'-phosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DARIPP synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DAROPP reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DARP reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPBC21C3.10c","type":"exact"}],"termid":"PR:Q9P7L3"}


id: GO:0010024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phytochromobilin, which involves the oxidative cleavage of heme by a heme oxygenase(HO) to form biliverdin IX alpha.","definition_xrefs":["PMID:11402195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tetrapyrrole biosynthetic process","termid":"GO:0033014"},{"relation_name":"is_a","term_name":"dicarboxylic acid biosynthetic process","termid":"GO:0043650"},{"relation_name":"is_a","term_name":"phytochromobilin metabolic process","termid":"GO:0051202"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0033013"],"is_obsolete":false,"name":"phytochromobilin biosynthetic process","synonyms":[{"name":"phytochromobilin anabolism","type":"exact"},{"name":"phytochromobilin biosynthesis","type":"exact"},{"name":"phytochromobilin formation","type":"exact"},{"name":"phytochromobilin synthesis","type":"exact"}],"termid":"GO:0010024"}


id: GO:0047461
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = diphosphate + (+)-delta-cadinene.","definition_xrefs":["EC:4.2.3.13","MetaCyc:4.6.1.11-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpene synthase activity","termid":"GO:0010334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"(+)-delta-cadinene synthase activity","secondary_identifiers":["RHEA:19525"],"synonyms":[{"name":"2-trans,6-trans-farnesyl-diphosphate diphosphate-lyase (cyclizing, (+)-delta-cadinene-forming)","type":"related"},{"name":"D-cadinene synthase activity","type":"related"}],"termid":"GO:0047461"}


id: PBO:0061685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 153","termid":"PBO:0061685"}


id: GO:0070214
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the protein-tyrosine kinase CSK and the GTPase-activating protein (GAP)-associated p62 (GAP-A.p62); may mediate translocation of proteins, including GAP and CSK, to membrane or cytoskeletal regions upon c-Src activation.","definition_xrefs":["PMID:7544435"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"},{"relation_name":"part_of","term_name":"cell leading edge","termid":"GO:0031252"}],"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":"CSK-GAP-A.p62 complex","termid":"GO:0070214"}


id: PBO:0074062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 39","termid":"PBO:0074062"}


id: PBO:0030721
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_actinomycin_D","termid":"PBO:0030721"}


id: GO:0141153
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"NADP+ + sn-glycerol 3-phosphate = dihydroxyacetone phosphate + H+ + NADPH.","definition_xrefs":["PMID:15557260","RHEA:11096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerol-3-phosphate dehydrogenase [NAD(P)+] activity","termid":"GO:0047952"}],"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":"glycerol-3-phosphate dehydrogenase (NADP+) activity","secondary_identifiers":["KEGG_REACTION:R00844"],"synonyms":[{"name":"L-glycerol-3-phosphate:NADP oxidoreductase activity","type":"exact"},{"name":"glycerol phosphate dehydrogenase (nicotinamide adenine dinucleotide phosphate) activity","type":"exact"},{"name":"glycerol-3-phosphate dehydrogenase [NADP+] activity","type":"exact"}],"termid":"GO:0141153"}


id: PBO:0069808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1094, pseudogene","termid":"PBO:0069808"}


id: GO:0019544
data:
  {"annotated_genes":["SJAG_00495"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80097],"is_not":false,"summary":null,"term":"GO:0019544"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-arginine into other compounds, including L-glutamate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-arginine catabolic process","termid":"GO:0006527"},{"relation_name":"is_a","term_name":"glutamate metabolic process","termid":"GO:0006536"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"L-arginine catabolic process to L-glutamate","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"arginine breakdown to glutamate","type":"exact"},{"name":"arginine degradation to glutamate","type":"exact"}],"termid":"GO:0019544","terms_by_termid":{"GO:0019544":null}}


id: GO:1904204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of skeletal muscle hypertrophy.","definition_xrefs":["GO_REF:0000058","PMID:23470307","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of skeletal muscle adaptation","termid":"GO:0014733"},{"relation_name":"is_a","term_name":"regulation of muscle hypertrophy","termid":"GO:0014743"},{"relation_name":"regulates","term_name":"skeletal muscle hypertrophy","termid":"GO:0014734"}],"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 skeletal muscle hypertrophy","termid":"GO:1904204"}


id: MONDO:0021525
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the body of uterus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine benign neoplasm","termid":"MONDO:0000632"},{"relation_name":"is_a","term_name":"corpus uteri neoplasm","termid":"MONDO:0021254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of corpus uteri","secondary_identifiers":["UMLS:C0153998","SCTID:92021007","ICD9:219.1","NCIT:C3608","MEDGEN:57808"],"synonyms":[{"name":"benign corpus uteri neoplasm","type":"exact"},{"name":"benign corpus uteri tumor","type":"exact"},{"name":"benign corpus uteri tumour","type":"exact"},{"name":"benign neoplasm of body of uterus","type":"exact"},{"name":"benign neoplasm of the body of uterus","type":"exact"},{"name":"benign neoplasm of the corpus uteri","type":"exact"},{"name":"benign neoplasm of the uterine body","type":"exact"},{"name":"benign neoplasm of the uterine corpus","type":"exact"},{"name":"benign neoplasm of uterine body","type":"exact"},{"name":"benign neoplasm of uterine corpus","type":"exact"},{"name":"benign tumor of body of uterus","type":"exact"},{"name":"benign tumor of corpus uteri","type":"exact"},{"name":"benign tumor of the body of uterus","type":"exact"},{"name":"benign tumor of the corpus uteri","type":"exact"},{"name":"benign tumor of the uterine body","type":"exact"},{"name":"benign tumor of the uterine corpus","type":"exact"},{"name":"benign tumor of uterine body","type":"exact"},{"name":"benign tumor of uterine corpus","type":"exact"},{"name":"benign tumour of body of uterus","type":"exact"},{"name":"benign tumour of corpus uteri","type":"exact"},{"name":"benign tumour of the body of uterus","type":"exact"},{"name":"benign tumour of the corpus uteri","type":"exact"},{"name":"benign tumour of the uterine body","type":"exact"},{"name":"benign tumour of the uterine corpus","type":"exact"},{"name":"benign tumour of uterine body","type":"exact"},{"name":"benign tumour of uterine corpus","type":"exact"},{"name":"benign uterine body neoplasm","type":"exact"},{"name":"benign uterine body tumor","type":"exact"},{"name":"benign uterine body tumour","type":"exact"},{"name":"benign uterine corpus neoplasm","type":"exact"},{"name":"benign uterine corpus tumor","type":"exact"},{"name":"benign uterine corpus tumour","type":"exact"},{"name":"body of uterus benign neoplasm","type":"exact"}],"termid":"MONDO:0021525","xrefs":{"Monarch":{"xref_id":"0021525"}}}


id: GO:1900399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of pyrimidine nucleotide biosynthetic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of nucleotide biosynthetic process","termid":"GO:0030810"},{"relation_name":"is_a","term_name":"regulation of pyrimidine nucleotide biosynthetic process","termid":"GO:1900397"},{"relation_name":"positively_regulates","term_name":"pyrimidine nucleotide biosynthetic process","termid":"GO:0006221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"positive regulation of pyrimidine nucleotide biosynthetic process","synonyms":[{"name":"activation of pyrimidine nucleotide anabolism","type":"exact"},{"name":"activation of pyrimidine nucleotide biosynthesis","type":"exact"},{"name":"activation of pyrimidine nucleotide biosynthetic process","type":"narrow"},{"name":"activation of pyrimidine nucleotide formation","type":"exact"},{"name":"activation of pyrimidine nucleotide synthesis","type":"exact"},{"name":"positive regulation of pyrimidine nucleotide anabolism","type":"exact"},{"name":"positive regulation of pyrimidine nucleotide biosynthesis","type":"exact"},{"name":"positive regulation of pyrimidine nucleotide formation","type":"exact"},{"name":"positive regulation of pyrimidine nucleotide synthesis","type":"exact"},{"name":"up regulation of pyrimidine nucleotide anabolism","type":"exact"},{"name":"up regulation of pyrimidine nucleotide biosynthesis","type":"exact"},{"name":"up regulation of pyrimidine nucleotide biosynthetic process","type":"exact"},{"name":"up regulation of pyrimidine nucleotide formation","type":"exact"},{"name":"up regulation of pyrimidine nucleotide synthesis","type":"exact"},{"name":"up-regulation of pyrimidine nucleotide anabolism","type":"exact"},{"name":"up-regulation of pyrimidine nucleotide biosynthesis","type":"exact"},{"name":"up-regulation of pyrimidine nucleotide biosynthetic process","type":"exact"},{"name":"up-regulation of pyrimidine nucleotide formation","type":"exact"},{"name":"up-regulation of pyrimidine nucleotide synthesis","type":"exact"},{"name":"upregulation of pyrimidine nucleotide anabolism","type":"exact"},{"name":"upregulation of pyrimidine nucleotide biosynthesis","type":"exact"},{"name":"upregulation of pyrimidine nucleotide biosynthetic process","type":"exact"},{"name":"upregulation of pyrimidine nucleotide formation","type":"exact"},{"name":"upregulation of pyrimidine nucleotide synthesis","type":"exact"}],"termid":"GO:1900399"}


id: PBO:0031826
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_RNA_modification","termid":"PBO:0031826"}


id: PBO:0054990
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 2404","termid":"PBO:0054990"}


id: PBO:0040442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase phospholipid transporting 8B3","termid":"PBO:0040442"}


id: GO:0034804
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: benzo(a)pyrene + O2 = benzo(a)pyrene-11,12-epoxide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete benzo(a)pyrene 11,12-epoxidase activity (obsolete GO:0034804)","termid":"GO:0034804"}


id: GO:0102661
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: all-trans-nonaprenyl diphosphate + homogentisate + H+ = 2-methyl-6-all-trans-nonaprenyl-1,4-benzoquinone + carbon dioxide + diphosphoric acid.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete homogentisate solanyltransferase activity (obsolete GO:0102661)","termid":"GO:0102661"}


id: MONDO:0001597
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the submandibular gland.","direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland disorder","termid":"MONDO:0001142"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"submandibular gland disorder","secondary_identifiers":["MESH:D013364","MEDGEN:52535","UMLS:C0038557","DOID:12897"],"synonyms":[{"name":"disease of submandibular gland","type":"exact"},{"name":"disease or disorder of submandibular gland","type":"exact"},{"name":"disorder of submandibular gland","type":"exact"},{"name":"submandibular gland disease","type":"exact"},{"name":"submandibular gland disease or disorder","type":"exact"}],"termid":"MONDO:0001597","xrefs":{"Monarch":{"xref_id":"0001597"}}}


id: MONDO:0019290
data:
  {"annotated_genes":["SJAG_00108","SJAG_03011","SJAG_00938","SJAG_02453","SJAG_03960","SJAG_00115"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88792,88791],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008962"},{"annotations":[87862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014885"},{"annotations":[87716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011997"},{"annotations":[88840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011683"},{"annotations":[86878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014070"}]},"cv_name":"mondo","definition":"A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections.","definition_xrefs":["MESH:D017496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin pigmentation disorder","termid":"MONDO:0019288"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00108":null,"SJAG_00115":null,"SJAG_00938":null,"SJAG_02453":null,"SJAG_03011":null,"SJAG_03960":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hypopigmentation of the skin","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:79376","UMLS:C0162835","HP:0001010","MedDRA:10040868","MEDGEN:102477"],"synonyms":[{"name":"hypomelanoses","type":"related"},{"name":"hypomelanosis","type":"related"},{"name":"hypopigmentation of the skin","type":"exact"},{"name":"hypopigmentation of the skin (disease)","type":"exact"}],"termid":"MONDO:0019290","terms_by_termid":{"MONDO:0008962":null,"MONDO:0011683":null,"MONDO:0011997":null,"MONDO:0014070":null,"MONDO:0014885":null},"xrefs":{"Monarch":{"xref_id":"0019290"}}}


id: PR:O74969
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ght2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74969"],"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":"high-affinity glucose transporter ght2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4B4.08","synonyms":[{"name":"Spom972h-ght2","type":"exact"},{"name":"hexose transporter 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74969"}


id: PBO:0043550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type IV alpha 1 chain","termid":"PBO:0043550"}


id: PBO:0053874
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 1150","termid":"PBO:0053874"}


id: GO:1902310
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of peptidyl-serine dephosphorylation.","definition_xrefs":["GOC:TermGenie","PMID:11953308","GOC:BHF","GOC:mtg_cardiac_conduct_nov11","GOC:rl"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of peptidyl-serine dephosphorylation (obsolete GO:1902310)","synonyms":[{"name":"activation of peptidyl-serine dephosphorylation","type":"narrow"},{"name":"up regulation of peptidyl-serine dephosphorylation","type":"exact"},{"name":"up-regulation of peptidyl-serine dephosphorylation","type":"exact"},{"name":"upregulation of peptidyl-serine dephosphorylation","type":"exact"}],"termid":"GO:1902310"}


id: PBO:0017518
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Twin Horse Tails","termid":"PBO:0017518"}


id: PBO:0035761
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_tyrosine","termid":"PBO:0035761"}


id: GO:2000281
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of histone H3-T3 phosphorylation.","definition_xrefs":["GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone H3-T3 phosphorylation (obsolete GO:2000281)","termid":"GO:2000281"}


id: GO:0042169
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a SH2 domain (Src homology 2) of a protein, a protein domain of about 100 amino-acid residues and belonging to the alpha + beta domain class.","definition_xrefs":["GOC:go_curators","Pfam:PF00017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"SH2 domain binding","termid":"GO:0042169"}


id: PBO:0001316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fructose-2,6-bisphosphate 2-phosphatase activity (predicted)","termid":"PBO:0001316"}


id: FYPO:0006364
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which meiotic spindle microtubules become disconnected from the spindle pole body during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:24954111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle morphology during meiosis I","termid":"FYPO:0005652"},{"relation_name":"is_a","term_name":"abnormal spindle pole body morphology during meiosis I","termid":"FYPO:0006022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000121"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000631","FYPO:0002399","FYPO:0005447","FYPO:0000121","FYPO:0000120","FYPO:0000002","FYPO:0000054"],"is_obsolete":false,"name":"spindle microtubules detached from spindle pole body during meiosis I","synonyms":[{"name":"meiotic spindle microtubules detached from spindle pole body during meiosis I","type":"exact"},{"name":"non-polar spindle during meiosis I","type":"related"},{"name":"spindle microtubules detached from SPB during meiosis I","type":"exact"},{"name":"spindle microtubules detached from spindle pole body during first meiotic nuclear division","type":"exact"},{"name":"spindle pole body detached from spindle microtubules during meiosis I","type":"exact"}],"termid":"FYPO:0006364"}


id: GO:0030946
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: protein tyrosine phosphate + H2O = protein tyrosine + phosphate. This reaction requires metal ions.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein tyrosine phosphatase activity","termid":"GO:0004725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0004721","GO:0140096","GO:0003824","GO:0016787","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"protein tyrosine phosphatase activity, metal-dependent","termid":"GO:0030946"}


id: GO:0008123
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cholesterol + O2 + reduced [NADPH--hemoprotein reductase] = 7alpha-hydroxycholesterol + H+ + H2O + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:21812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid 7-alpha-hydroxylase activity","termid":"GO:0008387"},{"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"cholesterol 7-alpha-monooxygenase activity","secondary_identifiers":["MetaCyc:CHOLESTEROL-7-ALPHA-MONOOXYGENASE-RXN","Reactome:R-HSA-192051","EC:1.14.14.23"],"synonyms":[{"name":"cholesterol 7-alpha-hydroxylase activity","type":"exact"},{"name":"cholesterol 7alpha-hydroxylase activity","type":"related"},{"name":"cholesterol 7alpha-monooxygenase activity","type":"related"},{"name":"cholesterol,NADPH:oxygen oxidoreductase (7alpha-hydroxylating)","type":"related"},{"name":"cytochrome P450 CYP7A1","type":"narrow"}],"termid":"GO:0008123"}


id: PBO:0077870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPM4 pseudogene 1","termid":"PBO:0077870"}


id: PBO:0090999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial TOM complex TPR repeat subunit Tom70","termid":"PBO:0090999"}


id: GO:1904420
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of telomeric loop formation.","definition_xrefs":["GO_REF:0000058","GOC:BHF_telomere","GOC:TermGenie","GOC:BHF","PMID:22579284","GOC:nc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of telomere maintenance","termid":"GO:0032206"},{"relation_name":"is_a","term_name":"regulation of telomeric loop formation","termid":"GO:1904418"},{"relation_name":"positively_regulates","term_name":"telomeric loop formation","termid":"GO:0031627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"positively_regulates","termid":"GO:0032200"},{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0032200"}],"interesting_parent_ids":["GO:0006259","GO:0032200","GO:0008150"],"is_obsolete":false,"name":"positive regulation of telomeric loop formation","synonyms":[{"name":"activation of t-loop biosynthesis","type":"narrow"},{"name":"activation of t-loop formation","type":"narrow"},{"name":"activation of telomeric loop formation","type":"narrow"},{"name":"positive regulation of t-loop biosynthesis","type":"exact"},{"name":"positive regulation of t-loop formation","type":"exact"},{"name":"up regulation of t-loop biosynthesis","type":"exact"},{"name":"up regulation of t-loop formation","type":"exact"},{"name":"up regulation of telomeric loop formation","type":"exact"},{"name":"up-regulation of t-loop biosynthesis","type":"exact"},{"name":"up-regulation of t-loop formation","type":"exact"},{"name":"up-regulation of telomeric loop formation","type":"exact"},{"name":"upregulation of t-loop biosynthesis","type":"exact"},{"name":"upregulation of t-loop formation","type":"exact"},{"name":"upregulation of telomeric loop formation","type":"exact"}],"termid":"GO:1904420"}


id: PATO:0000496
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000496 phase value (obsolete PATO:0000496)","termid":"PATO:0000496"}


id: GO:0047873
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dolichyl phosphate + H2O = dolichol + phosphate.","definition_xrefs":["MetaCyc:DOLICHYL-PHOSPHATASE-RXN","EC:3.1.3.51"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"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:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"dolichyl-phosphatase activity","secondary_identifiers":["RHEA:13797"],"synonyms":[{"name":"Dol-P phosphatase activity","type":"related"},{"name":"Dol-P-P phosphohydrolase activity","type":"exact"},{"name":"dolichol monophosphatase activity","type":"related"},{"name":"dolichol phosphatase activity","type":"related"},{"name":"dolichol phosphate phosphatase activity","type":"related"},{"name":"dolichyl monophosphate phosphatase activity","type":"related"},{"name":"dolichyl phosphate phosphatase activity","type":"related"},{"name":"dolichyl pyrophosphate phosphatase activity","type":"exact"},{"name":"dolichyl-phosphate phosphohydrolase activity","type":"related"},{"name":"polyisoprenyl phosphate phosphatase activity","type":"related"},{"name":"polyprenylphosphate phosphatase activity","type":"related"}],"termid":"GO:0047873"}


id: PBO:0085365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphoribosyl-glycinamide transformylase; catalyzes a step in the 'de novo' purine nucleotide biosynthetic pathway","termid":"PBO:0085365"}


id: MONDO:0011501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Skeletal dysplasia with wormian bone-multiple fractures-dentinogenesis imperfecta is a skeletal disorder, reported in three patients to date, characterized clinically by multiple fractures, wormian bones of the skull, dentinogenesis imperfecta and facial dysmorphism (hypertelorism, periorbital fullness). Although the signs are very similar to osteogenesis imperfecta, characteristic cortical defects in the absence of osteopenia and collagen abnormalities are considered to be distinctive. There have been no further descriptions in the literature since 1999.","definition_xrefs":["Orphanet:166277"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete malformative syndrome with dentinogenesis imperfecta (obsolete MONDO:0015877)","termid":"MONDO:0015877"},{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia","secondary_identifiers":["GARD:10290","OMIM:604922","MEDGEN:387969","MESH:C565734","UMLS:C1858032"],"synonyms":[{"name":"Suarez-Stickler syndrome","type":"exact"},{"name":"cortical defects wormian bones and dentinogenesis imperfecta","type":"related"},{"name":"cortical defects, WORMIAN bones, and dentinogenesis imperfecta","type":"related"}],"termid":"MONDO:0011501","xrefs":{"Monarch":{"xref_id":"0011501"}}}


id: GO:0102607
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3beta-hydroxy-12,15-cassadiene-11-one + NADPH + O2 + H+ = 2beta,3beta-dihydroxy-12,15-cassadiene-11-one + NADP + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3beta-hydroxy-12,15-cassadiene-11-one 2-hydroxylase activity (obsolete GO:0102607)","termid":"GO:0102607"}


id: GO:0018467
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: formaldehyde + H2O + NAD+ = formate + 2 H+ + NADH.","definition_xrefs":["RHEA:16425"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde dehydrogenase (NAD+) activity","termid":"GO:0004029"}],"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":"formaldehyde dehydrogenase (NAD+) activity","secondary_identifiers":["MetaCyc:FORMALDEHYDE-DEHYDROGENASE-RXN","KEGG_REACTION:R00604","UM-BBD_reactionID:r0240","EC:1.2.1.46"],"synonyms":[{"name":"formaldehyde:NAD+ oxidoreductase activity","type":"related"},{"name":"glutathione-independent formaldehyde dehydrogenase activity","type":"exact"}],"termid":"GO:0018467"}


id: PBO:0015234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3 involved in sporulation Dbl4","termid":"PBO:0015234"}


id: PR:Q09856
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U4/U6 small nuclear ribonucleoprotein Prp3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR14212:SF0","PRO:DAN"],"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":"U4/U5/U6 small nuclear ribonucleoprotein prp3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29E6.02","secondary_identifiers":["UniProtKB:Q09856"],"synonyms":[{"name":"SPAC29E6.02","type":"related"},{"name":"Spom972h-PRPF3","type":"exact"},{"name":"pre-mRNA-splicing factor 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09856"}


id: MONDO:0001083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients.","definition_xrefs":["NCIT:C3034"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"renal tubular transport disease","termid":"MONDO:0006510"},{"relation_name":"is_a","term_name":"renal tubule disorder","termid":"MONDO:0021568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"Fanconi renotubular syndrome","secondary_identifiers":["GARD:9120","NANDO:2100027","NANDO:2200187","DOID:1062","SCTID:40488004","SCTID:236466005","UMLS:C0015624","MESH:D005198","MEDGEN:4653"],"synonyms":[{"name":"De toni-Fanconi syndrome","type":"exact"},{"name":"De toni-debre-Fanconi syndrome","type":"exact"},{"name":"Fanconi syndrome","type":"exact"},{"name":"Fanconi's syndrome","type":"exact"},{"name":"Fanconi-de toni syndrome","type":"exact"},{"name":"Fanconi-de-toni syndrome","type":"exact"},{"name":"Lignac-Fanconi syndrome","type":"exact"},{"name":"adult Fanconi syndrome","type":"narrow"},{"name":"congenital Fanconi syndrome","type":"narrow"},{"name":"deToni Fanconi syndrome","type":"exact"},{"name":"infantile nephropathic cystinosis","type":"related"},{"name":"toni-debre-Fanconi syndrome","type":"related"}],"termid":"MONDO:0001083","xrefs":{"Monarch":{"xref_id":"0001083"}}}


id: PBO:0051517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 1 beta","termid":"PBO:0051517"}


id: PBO:0068878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 118, pseudogene","termid":"PBO:0068878"}


id: MONDO:0007401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Craniosynostosis, Dandy-Walker malformation and hydrocephalus is a malformation disorder characterized by sagittal craniosynostosis, Dandy-Walker malformation, hydrocephalus, craniofacial dysmorphism (including dolichocephaly, hypertelorism, micrognathia, positional ear deformity) and variable developmental delay. The inheritance pattern appears to be autosomal dominant.","definition_xrefs":["Orphanet:1538"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrocephalus","termid":"MONDO:0001150"},{"relation_name":"is_a","term_name":"familial scaphocephaly syndrome","termid":"MONDO:0015704"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0020022"],"is_obsolete":false,"name":"craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome","secondary_identifiers":["MEDGEN:325006","SCTID:720813007","UMLS:C1838347","MESH:C563973","GARD:998","OMIM:123155"],"synonyms":[{"name":"Braddock Jones Superneau syndrome","type":"related"},{"name":"Braddock-Jones-Superneau syndrome","type":"exact"},{"name":"Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus","type":"related"},{"name":"HDCPH1","type":"related"},{"name":"craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome","type":"exact"},{"name":"hydrocephalus, autosomal dominant","type":"related"},{"name":"sagittal craniosynostosis, Dandy-Walker malformation and hydrocephalus","type":"related"}],"termid":"MONDO:0007401","xrefs":{"Monarch":{"xref_id":"0007401"}}}


id: SO:0001203
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region (DNA) to which RNA polymerase binds, to begin transcription.","definition_xrefs":["xenbase:jb"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0001203 RNA_polymerase_promoter (obsolete SO:0001203)","synonyms":[{"name":"RNA polymerase promoter","type":"exact"}],"termid":"SO:0001203"}


id: MOD:01615
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-cysteine residue and a glycine residue by a dithioester bond to form glycyl cysteine dithioester.","definition_xrefs":["PubMed:11438688","PubMed:16388576","RESID:AA0512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thioester crosslinked residues","termid":"MOD:00395"},{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"}],"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":"glycyl cysteine dithioester","synonyms":[{"name":"(2R)-2-amino-3-[(aminoacetyl)disulfanyl]propanoic acid","type":"exact"},{"name":"2-(glycyldithio)alanine","type":"exact"},{"name":"S-glycyl cysteine persulfide","type":"exact"},{"name":"S-glycyl thiocysteine","type":"exact"},{"name":"glycyl cysteine dithioester","type":"exact"},{"name":"thioglycine cysteine disulfide","type":"exact"}],"termid":"MOD:01615"}


id: GO:0034382
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a chylomicron remnant is removed from the blood via receptor-mediated endocytosis into liver cells and its constituent parts degraded.","definition_xrefs":["GOC:BHF","GOC:mah","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triglyceride-rich lipoprotein particle clearance","termid":"GO:0071830"}],"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":"chylomicron remnant clearance","secondary_identifiers":["Reactome:R-HSA-8964026"],"termid":"GO:0034382"}


id: GO:0031870
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a thromboxane A2 receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostanoid receptor binding","termid":"GO:0031862"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"thromboxane A2 receptor binding","synonyms":[{"name":"prostanoid TP receptor binding","type":"exact"},{"name":"thromboxane A2 receptor ligand","type":"narrow"}],"termid":"GO:0031870"}


id: PBO:0113550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPOUT domain containing methyltransferase, poorly characterised, conflicting annotations between species, implicated in ribosome associted, centrosome associated, gene expression","termid":"PBO:0113550"}


id: PBO:0055496
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 2930","termid":"PBO:0055496"}


id: MONDO:0002506
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete early myoclonic encephalopathy (obsolete MONDO:0002506)","termid":"MONDO:0002506","xrefs":{"Monarch":{"xref_id":"0002506"}}}


id: GO:0045031
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with ATP and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled purinergic nucleotide receptor activity","termid":"GO:0045028"}],"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":"G protein-coupled ATP receptor activity","synonyms":[{"name":"ATP-activated adenosine receptor activity","type":"related"},{"name":"ATP-activated nucleotide receptor activity","type":"broad"}],"termid":"GO:0045031"}


id: FYPO:0006500
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which disassembly of the cell wall at the site of cell-cell fusion during mating begins earlier than normal, e.g. before pairing with a partner cell. Premature cell wall breakdown often results in cell lysis.","definition_xrefs":["PMID:29453312","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell wall disassembly at cell fusion site","termid":"FYPO:0006499"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0004805"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0004805","FYPO:0000002","FYPO:0000301"],"is_obsolete":false,"name":"premature cell wall disassembly at cell fusion site","synonyms":[{"name":"advanced cell wall disassembly at cell fusion site","type":"exact"},{"name":"premature cell wall disassembly at cell fusion site during conjugation with cellular fusion","type":"exact"},{"name":"premature cell wall disassembly at cell fusion site during mating","type":"exact"},{"name":"premature cell wall disassembly at cell-cell fusion focus","type":"exact"},{"name":"premature cell wall disassembly at cell-cell fusion site","type":"exact"},{"name":"premature fungal-type cell wall disassembly at cell fusion site","type":"exact"},{"name":"premature fungal-type cell wall disassembly involved in conjugation with cellular fusion","type":"exact"}],"termid":"FYPO:0006500"}


id: PBO:0087724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the SAGA transcriptional regulatory complex; not present in SAGA-like complex SLIK/SALSA; required for SAGA-mediated inhibition at some promoters","termid":"PBO:0087724"}


id: FYPO:0007815
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to protein aggregate centers is normal (i.e. indistinguishable from wild type). Protein aggregate centers are composed of chaperones and misfolded proteins, and are reversibly formed in the nucleus and cytosol to shield thermosensitive proteins from degradation until conditions allow disaggregation and refolding.","definition_xrefs":["PomBase:mah","PMID:33386485"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during vegetative growth","termid":"FYPO:0000644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000138","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to protein aggregate center","synonyms":[{"name":"normal protein localisation to protein aggregate centre","type":"exact"},{"name":"normal protein localization to PAC","type":"exact"},{"name":"normal protein localization to PACs","type":"exact"},{"name":"normal protein localization to protein aggregate center during mitotic cell cycle","type":"related"},{"name":"normal protein localization to protein aggregate center during vegetative growth","type":"exact"}],"termid":"FYPO:0007815"}


id: GO:1990182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whereby a membrane-bounded vesicle is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane.","definition_xrefs":["PMID:12154376","PMID:16773132","PMID:18617898","PMID:10572093","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exocytosis","termid":"GO:0006887"},{"relation_name":"is_a","term_name":"establishment of vesicle localization","termid":"GO:0051650"},{"relation_name":"part_of","term_name":"extracellular exosome biogenesis","termid":"GO:0097734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0016192","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"exosomal secretion","synonyms":[{"name":"exosomal protein secretion","type":"narrow"},{"name":"exosomal secretory pathway","type":"exact"},{"name":"extracellular vesicular exosome secretion","type":"exact"},{"name":"multi-vesicular body fusion with plasma membrane","type":"exact"},{"name":"secretion of exosome","type":"exact"}],"termid":"GO:1990182"}


id: PBO:0044908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dexi homolog","termid":"PBO:0044908"}


id: GO:0034344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of type III interferon production. Interferon lambda is the only member of the type III interferon found so far.","definition_xrefs":["ISBN:0126896631","PMID:15546383","PMID:16734557","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"type III interferon production","termid":"GO:0034343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of type III interferon production","synonyms":[{"name":"regulation of type III IFN production","type":"exact"}],"termid":"GO:0034344"}


id: GO:0061370
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of testosterone, an androgen having 17beta-hydroxy and 3-oxo groups, together with unsaturation at C-4 C-5.","definition_xrefs":["GOC:yaf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid biosynthetic process","termid":"GO:0006694"},{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"olefinic compound biosynthetic process","termid":"GO:0120255"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"testosterone biosynthetic process","termid":"GO:0061370"}


id: GO:0007163
data:
  {"annotated_genes":["SJAG_00332","SJAG_00028","SJAG_00333","SJAG_02651","SJAG_00268","SJAG_02624","SJAG_01738","SJAG_01722","SJAG_02022","SJAG_00236","SJAG_01388","SJAG_02392","SJAG_01799","SJAG_01613","SJAG_00424","SJAG_03581","SJAG_00910","SJAG_00661","SJAG_02838","SJAG_00140","SJAG_03718","SJAG_01373","SJAG_00317","SJAG_02222","SJAG_04666","SJAG_04509","SJAG_01196","SJAG_03126","SJAG_01376","SJAG_03540","SJAG_00030","SJAG_00216","SJAG_04461","SJAG_02366","SJAG_02695","SJAG_04980","SJAG_04624","SJAG_00185","SJAG_02760","SJAG_00845","SJAG_03625","SJAG_03705","SJAG_00152","SJAG_04653","SJAG_03086","SJAG_03748","SJAG_04703","SJAG_00596","SJAG_01732","SJAG_03486","SJAG_04322","SJAG_02819","SJAG_03754","SJAG_00229","SJAG_02536","SJAG_00851","SJAG_00610","SJAG_01901","SJAG_01794","SJAG_02737","SJAG_03048","SJAG_03453","SJAG_01456","SJAG_04522","SJAG_03637","SJAG_04724","SJAG_00514","SJAG_00355","SJAG_00594","SJAG_03596","SJAG_03170"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61615,78236,92917,99702,105542,106171,106972,108705,110918],"is_not":false,"summary":null,"term":"GO:0007163"},{"annotations":[105283,119752,112588,101526,89821,108665,118323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051523"},{"annotations":[121198,106451,94362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061171"},{"annotations":[81853,92613,80058,116640,98978,94041,95248,72416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030010"},{"annotations":[106343,78018,118792,98757,106674],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000132"},{"annotations":[97629,90236,91208,107158,112589,74918,101107,101965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030950"},{"annotations":[109422,112690,115884,91640,101433,97630,101527,120507,106454,119754,114139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061245"},{"annotations":[103063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030952"},{"annotations":[78602,101002,81141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030951"},{"annotations":[73132,74990,72068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030011"},{"annotations":[92731],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1904846"},{"annotations":[109424,105494,114309],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0061173"},{"annotations":[109425,118429],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2000784"},{"annotations":[95516,101967,107160],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2000247"},{"annotations":[105496],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0061361"},{"annotations":[70750,96359],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000114"},{"annotations":[104186],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000099"},{"annotations":[96360,114884,97441,120655,106334,92911],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000100"},{"annotations":[92703,111244,71191,102179,95251,58870],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032878"},{"annotations":[89666,104645,107917,94198],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000769"}]},"cv_name":"biological_process","definition":"Any cellular process that results in the specification, formation or maintenance of anisotropic intracellular organization or cell growth patterns.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular 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or maintenance of cell polarity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:30664646":null},"secondary_identifiers":["GO:0030012","GO:0030467"],"synonyms":[{"name":"cell polarity","type":"related"},{"name":"establishment and/or maintenance of cell polarity","type":"related"},{"name":"establishment and/or maintenance of cell polarization","type":"related"}],"termid":"GO:0007163","terms_by_termid":{"GO:0000132":null,"GO:0007163":null,"GO:0030010":null,"GO:0030011":null,"GO:0030950":null,"GO:0030951":null,"GO:0030952":null,"GO:0032878":null,"GO:0051523":null,"GO:0061171":null,"GO:0061173":null,"GO:0061245":null,"GO:0061361":null,"GO:1904846":null,"GO:2000099":null,"GO:2000100":null,"GO:2000114":null,"GO:2000247":null,"GO:2000769":null,"GO:2000784":null}}


id: GO:0032880
data:
  {"annotated_genes":["SJAG_01084","SJAG_01245","SJAG_01311","SJAG_03602","SJAG_03453","SJAG_04343","SJAG_04597","SJAG_01373","SJAG_02392","SJAG_01805","SJAG_04312","SJAG_04464","SJAG_03048","SJAG_04509","SJAG_02645","SJAG_03970","SJAG_02592"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042997"},{"annotations":[107616],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042308"},{"annotations":[97635,92732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903067"},{"annotations":[96184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140325"},{"annotations":[116311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900181"},{"annotations":[97636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903077"},{"annotations":[95582,102228,112844,103647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046827"},{"annotations":[104182,92618,96147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042307"},{"annotations":[100212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120047"},{"annotations":[89668,93795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033157"},{"annotations":[109771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905391"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of any process in which a protein is transported to, or maintained in, a specific location.","definition_xrefs":["GOC:dph","GOC:mah","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of localization","termid":"GO:0032879"},{"relation_name":"regulates","term_name":"intracellular protein localization","termid":"GO:0008104"}],"gene_count":17,"genes_by_uniquename":{"SJAG_01084":null,"SJAG_01245":null,"SJAG_01311":null,"SJAG_01373":null,"SJAG_01805":null,"SJAG_02392":null,"SJAG_02592":null,"SJAG_02645":null,"SJAG_03048":null,"SJAG_03453":null,"SJAG_03602":null,"SJAG_03970":null,"SJAG_04312":null,"SJAG_04343":null,"SJAG_04464":null,"SJAG_04509":null,"SJAG_04597":null},"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 localization","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1903827"],"synonyms":[{"name":"regulation of cellular protein localisation","type":"exact"},{"name":"regulation of cellular protein localization","type":"exact"},{"name":"regulation of protein localisation","type":"exact"}],"termid":"GO:0032880","terms_by_termid":{"GO:0033157":null,"GO:0042307":null,"GO:0042308":null,"GO:0042997":null,"GO:0046827":null,"GO:0120047":null,"GO:0140325":null,"GO:1900181":null,"GO:1903067":null,"GO:1903077":null,"GO:1905391":null}}


id: PBO:0075447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis associated 2","termid":"PBO:0075447"}


id: GO:0052427
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in symbiont peptidase activity, the catalysis of the hydrolysis of peptide bonds in a protein. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by host of symbiont peptidase activity (obsolete GO:0052427)","synonyms":[{"name":"modulation by host of symbiont protease activity","type":"narrow"}],"termid":"GO:0052427"}


id: PBO:0064728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 64","termid":"PBO:0064728"}


id: GO:0002619
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of non-professional antigen presenting cell antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antigen processing and presentation","termid":"GO:0002577"},{"relation_name":"regulates","term_name":"non-professional antigen presenting cell antigen processing and presentation","termid":"GO:0002473"}],"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 non-professional antigen presenting cell antigen processing and presentation","termid":"GO:0002619"}


id: PBO:0071867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 5","termid":"PBO:0071867"}


id: GO:0047268
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: raffinose + 1-alpha-D-galactosyl-myo-inositol = stachyose + myo-inositol.","definition_xrefs":["EC:2.4.1.67","MetaCyc:2.4.1.67-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"galactosyltransferase activity","termid":"GO:0008378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016757","GO:0003824"],"is_obsolete":false,"name":"galactinol-raffinose galactosyltransferase activity","secondary_identifiers":["RHEA:20776"],"synonyms":[{"name":"alpha-D-(1->3)-galactosyl-myo-inositol:raffinose galactosyltransferase activity","type":"related"},{"name":"stachyose synthetase activity","type":"related"}],"termid":"GO:0047268"}


id: GO:0036346
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 a L-cysteine stimulus. L-cysteine is an optically active form of cysteine having L-configuration.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amino acid stimulus","termid":"GO:0071230"},{"relation_name":"is_a","term_name":"response to L-cysteine","termid":"GO:1901367"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to L-cysteine","termid":"GO:0036346"}


id: GO:0032718
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of interleukin-9 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of interleukin-9 production","termid":"GO:0032678"},{"relation_name":"negatively_regulates","term_name":"interleukin-9 production","termid":"GO:0032638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of interleukin-9 production","secondary_identifiers":["GO:0045418"],"synonyms":[{"name":"down regulation of interleukin-9 production","type":"exact"},{"name":"down-regulation of interleukin-9 production","type":"exact"},{"name":"downregulation of interleukin-9 production","type":"exact"},{"name":"inhibition of interleukin-9 production","type":"narrow"},{"name":"negative regulation of IL-9 production","type":"exact"},{"name":"negative regulation of interleukin-9 biosynthetic process","type":"narrow"}],"termid":"GO:0032718"}


id: MONDO:0002770
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Normal or abnormal secretions from the vagina. Mucus produced by the cervical glands is discharged from the vagina naturally, especially during the childbearing years. Causes of abnormal vaginal discharge include infectious agents (e.g., Neisseria gonorrhea, Chlamydia trachomatis, Trichomonas, and Candida albicans), the presence of foreign bodies, and cervical or vaginal cancer.","definition_xrefs":["NCIT:C50795"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal disorder","termid":"MONDO:0001433"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vaginal discharge","secondary_identifiers":["UMLS:C0227791","MEDGEN:65302","icd11.foundation:2123556104","DOID:3767","MESH:D019522"],"synonyms":[{"name":"Discharge, vaginal","type":"exact"}],"termid":"MONDO:0002770","xrefs":{"Monarch":{"xref_id":"0002770"}}}


id: FYPO:0003392
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of ubiquinone binding by a gene product (usually a protein) in a mutant is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal ubiquinone binding","termid":"FYPO:0003391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"decreased ubiquinone binding","synonyms":[{"name":"decreased coenzyme Q binding","type":"exact"},{"name":"reduced ubiquinone binding","type":"exact"}],"termid":"FYPO:0003392"}


id: GO:0001692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving histamine, a physiologically active amine, found in plant and animal tissue and released from mast cells as part of an allergic reaction in humans.","definition_xrefs":["ISBN:0395825172","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biogenic amine metabolic process","termid":"GO:0006576"},{"relation_name":"is_a","term_name":"imidazole-containing compound metabolic process","termid":"GO:0052803"},{"relation_name":"is_a","term_name":"ammonium ion metabolic process","termid":"GO:0097164"}],"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":"histamine metabolic process","synonyms":[{"name":"histamine metabolism","type":"exact"}],"termid":"GO:0001692"}


id: GO:0035921
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled breakdown of a desmosome. A desmosome is a patch-like intercellular junction found in vertebrate tissues, consisting of parallel zones of two cell membranes, separated by an space of 25-35 nm, and having dense fibrillar plaques in the subjacent cytoplasm.","definition_xrefs":["GOC:vk","GOC:BHF","ISBN:0198506732","PMID:9182671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"desmosome organization","termid":"GO:0002934"},{"relation_name":"is_a","term_name":"cell-cell junction disassembly","termid":"GO:0150147"}],"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":"desmosome disassembly","synonyms":[{"name":"desmosome dissociation","type":"exact"}],"termid":"GO:0035921"}


id: GO:0005596
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(XIV) chains; type XIV collagen triple helices may link sheet-forming or fibrillar collagens to other structures.","definition_xrefs":["ISBN:0721639976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"FACIT collagen trimer","termid":"GO:0005593"}],"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 XIV trimer","termid":"GO:0005596"}


id: PBO:0035924
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H2B-K119_ubiquitination_during_vegetative_growth","termid":"PBO:0035924"}


id: PBO:0077592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane serine protease 3","termid":"PBO:0077592"}


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:0000257"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"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: FYPO:0004853
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype that affects the localization of an RNA in a cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localization phenotype","termid":"FYPO:0000138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"RNA localization phenotype","synonyms":[{"name":"RNA localisation phenotype","type":"exact"},{"name":"fission yeast RNA localization phenotype","type":"exact"}],"termid":"FYPO:0004853"}


id: PBO:0054913
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 2327","termid":"PBO:0054913"}


id: PBO:0088084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBX domain-containing substrate adaptor for Cdc48p; ubiquitin regulatory X domain-containing protein that acts as a substrate recruiting cofactor for Cdc48p; positively regulates Glc7p PPase activity to promote growth and mitotic progression in complex with Cdc48p; ubiquitinated protein interactor involved in ER-associated degradation (ERAD); regulated by nuclear Ub-dependent degradation (INMAD pathway) independent of the Asi and Doa10 complexes; homolog of human p47 (NSFL1C)","termid":"PBO:0088084"}


id: FYPO:0006437
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the mitotic DNA damage checkpoint is normal (i.e. indistinguishable from wild type) when the cell is exposed to methyl methanesulfonate. The S phase DNA damage checkpoint slows progression through S phase in response to DNA damage.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic DNA damage checkpoint","termid":"FYPO:0001705"},{"relation_name":"is_a","term_name":"normal mitotic cell cycle regulation during cellular response to methyl methanesulfonate","termid":"FYPO:0005373"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000298","FYPO:0000631"],"is_obsolete":false,"name":"normal mitotic DNA damage checkpoint during cellular response to methyl methanesulfonate","synonyms":[{"name":"normal mitotic DNA damage checkpoint activation during cellular response to methyl methanesulfonate","type":"exact"},{"name":"normal mitotic DNA damage checkpoint during cellular response to MMS","type":"exact"},{"name":"normal mitotic DNA damage checkpoint during cellular response to methyl methanesulfonate during mitotic cell cycle","type":"exact"},{"name":"normal mitotic DNA damage checkpoint during cellular response to methyl methanesulfonate during vegetative growth","type":"exact"}],"termid":"FYPO:0006437"}


id: PBO:0056106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LYPLA1 pseudogene 1","termid":"PBO:0056106"}


id: PBO:0059173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class I-related","termid":"PBO:0059173"}


id: MONDO:0006652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myocardial infarction in which the anterior wall of the heart is involved. Anterior wall myocardial infarction is often caused by occlusion of the left anterior descending coronary artery. It can be categorized as anteroseptal or anterolateral wall myocardial infarction.","definition_xrefs":["MESH:D056988"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myocardial infarction","termid":"MONDO:0005068"}],"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":"anterolateral myocardial infarction","secondary_identifiers":["MedDRA:10068109","icd11.foundation:687792216","DOID:5845","EFO:1000812","MEDGEN:78086","UMLS:C0262564"],"synonyms":[{"name":"acute anterior wall myocardial infarction","type":"related"},{"name":"anterolateral myocardial infarction","type":"exact"},{"name":"anterolateral myocardial infarctions","type":"related"},{"name":"anteroseptal myocardial infarction","type":"related"},{"name":"anteroseptal myocardial infarctions","type":"related"},{"name":"infarction, anterolateral myocardial","type":"related"},{"name":"infarction, anteroseptal myocardial","type":"related"},{"name":"infarctions, anterolateral myocardial","type":"related"},{"name":"infarctions, anteroseptal myocardial","type":"related"},{"name":"myocardial infarction, anterior wall","type":"related"},{"name":"myocardial infarction, anterolateral","type":"related"},{"name":"myocardial infarction, anteroseptal","type":"related"},{"name":"myocardial infarctions, anterolateral","type":"related"},{"name":"myocardial infarctions, anteroseptal","type":"related"}],"termid":"MONDO:0006652","xrefs":{"Monarch":{"xref_id":"0006652"}}}


id: PBO:0057920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3622b","termid":"PBO:0057920"}


id: GO:0070160
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cell-cell junction that seals cells together in an epithelium in a way that prevents even small molecules from leaking from one side of the sheet to the other.","definition_xrefs":["ISBN:0815332181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell junction","termid":"GO:0005911"}],"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":"tight junction","secondary_identifiers":["Wikipedia:Tight_junction"],"synonyms":[{"name":"occluding cell junction","type":"exact"},{"name":"occluding junction","type":"exact"}],"termid":"GO:0070160"}


id: FYPO:0000416
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid separation begins before anaphase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid separation","termid":"FYPO:0000670"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"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:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000337","FYPO:0000641","FYPO:0000631","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"premature mitotic sister chromatid separation","synonyms":[{"name":"advanced mitotic sister chromatid separation","type":"exact"},{"name":"chromosome segregation: premature","type":"broad"},{"name":"premature chromosome separation during vegetative growth","type":"exact"},{"name":"premature mitotic chromosome separation","type":"exact"},{"name":"premature sister chromatid separation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000416"}


id: PBO:0051846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iroquois homeobox 2","termid":"PBO:0051846"}


id: MONDO:0005517
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm that affects the pharynx.","definition_xrefs":["NCIT:C7545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system cancer","termid":"MONDO:0000376"},{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"},{"relation_name":"is_a","term_name":"disorder of pharynx","termid":"MONDO:0020592"},{"relation_name":"is_a","term_name":"pharynx neoplasm","termid":"MONDO:0021246"},{"relation_name":"is_a","term_name":"malignant tumor of neck","termid":"MONDO:0021310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"pharynx cancer","secondary_identifiers":["EFO:0005577","MEDGEN:57554","DOID:0060119","MESH:D010610","UMLS:C0153405"],"synonyms":[{"name":"cancer of chordate pharynx","type":"exact"},{"name":"cancer of pharynx","type":"exact"},{"name":"chordate pharynx cancer","type":"exact"},{"name":"malignant chordate pharynx neoplasm","type":"exact"},{"name":"malignant neoplasm of chordate pharynx","type":"exact"},{"name":"malignant neoplasm of pharynx","type":"exact"},{"name":"malignant pharyngeal neoplasm","type":"exact"},{"name":"malignant pharyngeal tumor","type":"exact"},{"name":"malignant pharyngeal tumour","type":"exact"},{"name":"malignant pharynx neoplasm","type":"exact"},{"name":"malignant pharynx tumor","type":"exact"},{"name":"malignant pharynx tumour","type":"exact"},{"name":"malignant tumor of pharynx","type":"exact"},{"name":"malignant tumor of the pharynx","type":"exact"},{"name":"malignant tumour of pharynx","type":"exact"},{"name":"malignant tumour of the pharynx","type":"exact"},{"name":"pharyngeal cancer","type":"related"},{"name":"pharyngeal neoplasm","type":"exact"},{"name":"pharynx cancer","type":"exact"},{"name":"pharynx neoplasm","type":"broad"}],"termid":"MONDO:0005517","xrefs":{"Monarch":{"xref_id":"0005517"}}}


id: MONDO:0004370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the sphenocavernous region.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skull base meningioma","termid":"MONDO:0002998"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphenocavernous meningioma","secondary_identifiers":["DOID:7820","MEDGEN:234801","UMLS:C1336036","NCIT:C5313"],"termid":"MONDO:0004370","xrefs":{"Monarch":{"xref_id":"0004370"}}}


id: PBO:0003608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenosylhomocysteinase (predicted)","termid":"PBO:0003608"}


id: FYPO:0007989
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which karyogamy involved in conjugation with cellular fusion does not occur because the nuclei fail to come in physical contact.","definition_xrefs":["PomBase:mlr","PMID:25869666"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear congression during mating","termid":"FYPO:0003062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0000301","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abolished nuclear congression during mating","termid":"FYPO:0007989"}


id: MONDO:0004622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"},{"relation_name":"is_a","term_name":"vascular insufficiency disorder","termid":"MONDO:0020674"}],"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":"chronic intestinal vascular insufficiency","secondary_identifiers":["UMLS:C0311262","DOID:8633","ICD9:557.1","SCTID:111354009","MEDGEN:90228"],"synonyms":[{"name":"CMI - chronic mesenteric ischaemia","type":"exact"},{"name":"chronic mesenteric ischemia","type":"exact"}],"termid":"MONDO:0004622","xrefs":{"Monarch":{"xref_id":"0004622"}}}


id: PBO:0060102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 3","termid":"PBO:0060102"}


id: PR:Q7Z9H9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A polyphosphoinositide phosphatase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01912"],"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":"polyphosphoinositide phosphatase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1093.03","secondary_identifiers":["UniProtKB:Q7Z9H9"],"synonyms":[{"name":"Spom972h-FIG4","type":"exact"},{"name":"phosphatidylinositol 3,5-bisphosphate 5-phosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q7Z9H9"}


id: MONDO:0008291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Porokeratosis plantaris palmaris et disseminata (PPPD) is a rare form of porokeratosis occurring mainly in adolescence and characterized by small pruritic or painful keratotic papules that first appear on the palms and soles, and may gradually become generalized.","definition_xrefs":["Orphanet:737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porokeratosis","termid":"MONDO:0006602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"porokeratosis plantaris palmaris et disseminata","secondary_identifiers":["OMIM:175850","GARD:16542","UMLS:C0162838","MEDGEN:56517","SCTID:718218005"],"synonyms":[{"name":"POROK2","type":"related"},{"name":"palmar, plantar and disseminated porokeratosis","type":"exact"},{"name":"porokeratosis 2, palmar, plantar, and disseminated","type":"exact"},{"name":"porokeratosis 2, palmar, plantar, and disseminated type","type":"related"},{"name":"porokeratosis palmaris Et plantaris disseminata","type":"related"},{"name":"porokeratosis plantaris palmaris et disseminata","type":"exact"},{"name":"porokeratosis, palmar, plantar, and disseminated","type":"related"},{"name":"porokeratosis, palmar, plantar, and disseminated, 1","type":"related"}],"termid":"MONDO:0008291","xrefs":{"Monarch":{"xref_id":"0008291"}}}


id: MONDO:0007236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"branchio-oto-renal syndrome","termid":"MONDO:0007029"}],"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":"branchiootorenal syndrome 1","secondary_identifiers":["MEDGEN:1632634","UMLS:C4551702","DOID:0111423","OMIM:113650"],"synonyms":[{"name":"BOR1","type":"related"},{"name":"Melnick-Fraser syndrome","type":"related"},{"name":"branchiootorenal dysplasia","type":"related"},{"name":"branchiootorenal syndrome 1","type":"exact"},{"name":"branchiootorenal syndrome 1, with or without cataracts","type":"exact"},{"name":"branchiootorenal syndrome type 1","type":"exact"}],"termid":"MONDO:0007236","xrefs":{"Monarch":{"xref_id":"0007236"}}}


id: GO:0002684
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of an immune system process.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of immune system process","termid":"GO:0002682"},{"relation_name":"is_a","term_name":"positive regulation of biological process","termid":"GO:0048518"},{"relation_name":"positively_regulates","term_name":"immune system process","termid":"GO:0002376"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of immune system process","synonyms":[{"name":"activation of immune system process","type":"narrow"},{"name":"stimulation of immune system process","type":"narrow"},{"name":"up regulation of immune system process","type":"exact"},{"name":"up-regulation of immune system process","type":"exact"},{"name":"upregulation of immune system process","type":"exact"}],"termid":"GO:0002684"}


id: PBO:0078842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Pro (anticodon TGG) 4-1","termid":"PBO:0078842"}


id: PBO:0030538
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cAMP_level_during_glucose_starvation","termid":"PBO:0030538"}


id: MONDO:0003875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mature teratoma that arises from the central nervous system during childhood.","definition_xrefs":["NCIT:C27404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system mature teratoma","termid":"MONDO:0003733"},{"relation_name":"is_a","term_name":"childhood central nervous system germ cell tumor","termid":"MONDO:0003750"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood central nervous system mature teratoma","secondary_identifiers":["MEDGEN:232345","UMLS:C1332955","DOID:6423"],"synonyms":[{"name":"central nervous system mature teratoma of childhood","type":"exact"},{"name":"childhood central nervous system mature teratoma","type":"exact"},{"name":"paediatric central nervous system mature teratoma","type":"exact"},{"name":"pediatric central nervous system mature teratoma","type":"exact"}],"termid":"MONDO:0003875","xrefs":{"Monarch":{"xref_id":"0003875"}}}


id: PBO:0046461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eosinophil peroxidase","termid":"PBO:0046461"}


id: MONDO:0015946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic epidermal disorder (obsolete MONDO:0015946)","secondary_identifiers":["Orphanet:183426"],"synonyms":[{"name":"genetic epidermal disorder","type":"related"}],"termid":"MONDO:0015946","xrefs":{"Monarch":{"xref_id":"0015946"}}}


id: PBO:0111328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small subunit processome, U3 snoRNP-associated protein Nop58","termid":"PBO:0111328"}


id: MONDO:0011049
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by psychomotor delay, brachycephaly with flat face, small nose, microstomia, cleft palate, cataract, hearing loss, hypoplastic scrotum and digital anomalies.","definition_xrefs":["Orphanet:1272"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fine-Lubinsky syndrome","secondary_identifiers":["MESH:C537933","UMLS:C0795941","GARD:958","SCTID:720955004","OMIM:601353","MEDGEN:163198"],"synonyms":[{"name":"brachycephaly, deafness, cataract and intellectual disability","type":"related"},{"name":"brachycephaly, deafness, cataract and mental retardation","type":"related"},{"name":"brachycephaly, deafness, cataract, microstomia, and intellectual disability","type":"related"},{"name":"brachycephaly, deafness, cataract, microstomia, and mental retardation","type":"related"},{"name":"brachycephaly-deafness-cataract-intellectual disability syndrome","type":"exact"},{"name":"fine-Lubinsky syndrome","type":"exact"}],"termid":"MONDO:0011049","xrefs":{"Monarch":{"xref_id":"0011049"}}}


id: FYPO:0008015
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 import of glucose into the cell is decreased with respect to wild-type.","definition_xrefs":["PomBase:mlr","PMID:35781263"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glucose import","termid":"FYPO:0001827"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased glucose import","termid":"FYPO:0008015"}


id: GO:0030600
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: feruloyl-polysaccharide + H2O = ferulate + polysaccharide.","definition_xrefs":["EC:3.1.1.73"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"feruloyl esterase activity","secondary_identifiers":["MetaCyc:3.1.1.73-RXN"],"synonyms":[{"name":"4-hydroxy-3-methoxycinnamoyl-sugar hydrolase activity","type":"related"},{"name":"FAE-I","type":"related"},{"name":"FAE-II","type":"related"},{"name":"FAE-III","type":"related"},{"name":"FAEA","type":"related"},{"name":"cinnAE","type":"related"},{"name":"cinnamoyl ester hydrolase activity","type":"exact"},{"name":"ferulic acid esterase activity","type":"related"},{"name":"hemicellulase accessory","type":"related"},{"name":"hydroxycinnamoyl esterase activity","type":"related"}],"termid":"GO:0030600"}


id: MONDO:0010469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autism, susceptiblity to","termid":"MONDO:0020836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epsilon-trimethyllysine hydroxylase deficiency","secondary_identifiers":["UMLS:C3550875","OMIM:300872","MEDGEN:763789"],"synonyms":[{"name":"AUTSX6","type":"related"},{"name":"EPSILON-trimethyllysine HYDROXYLASE deficiency","type":"related"},{"name":"TMLHED","type":"related"},{"name":"autism, susceptibility to, X-linked 6","type":"related"},{"name":"autism, susceptibility to, X-linked 6, X-linked recessive","type":"exact"},{"name":"epsilon-trimethyllysine hydroxylase deficiency","type":"exact"},{"name":"susceptibility to X-linked autism 6","type":"related"}],"termid":"MONDO:0010469","xrefs":{"Monarch":{"xref_id":"0010469"}}}


id: MONDO:1010012
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Conotruncal heart malformations that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conotruncal heart malformations, non-human animal","secondary_identifiers":["OMIA:000224"],"termid":"MONDO:1010012","xrefs":{"Monarch":{"xref_id":"1010012"}}}


id: PBO:0067927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 229","termid":"PBO:0067927"}


id: PBO:0036068
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitotic_spindle_collapse_during_anaphase_B","termid":"PBO:0036068"}


id: FYPO:0008103
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the preinuclear endoplasmic reticulum is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:36799444"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0006378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000138","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to perinuclear endoplasmic reticulum","termid":"FYPO:0008103"}


id: GO:1990383
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 deprivation of biotin.","definition_xrefs":["PMID:12557275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to starvation","termid":"GO:0009267"}],"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 biotin starvation","termid":"GO:1990383"}


id: PBO:0070318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY3 pseudogene 7","termid":"PBO:0070318"}


id: FYPO:0002221
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through the anaphase of meiosis II is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of meiotic cell cycle phase","termid":"FYPO:0002220"}],"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:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased duration of meiotic anaphase II","synonyms":[{"name":"delayed meiotic anaphase II progression","type":"related"},{"name":"increased duration of meiotic anaphase II progression","type":"exact"},{"name":"prolonged meiotic anaphase II","type":"exact"}],"termid":"FYPO:0002221"}


id: PBO:0043522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly factor 4 homolog","termid":"PBO:0043522"}


id: MONDO:0009626
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Mendelian disease characterized by the presence of microcephaly and intracranial calcifications at birth accompanied by neurological delay, seizures and a clinical course similar to that seen in patients after intrauterine infection with Toxoplasma gondii, Rubella, Cytomegalovirus, Herpes simplex (so-called TORCH syndrome), or other agents, despite repeated tests revealing the absence of any known infectious agent.","definition_xrefs":["Orphanet:1229"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"pseudo-TORCH syndrome","secondary_identifiers":["GARD:12426","MEDGEN:483678","OMIMPS:251290","DOID:0050656","SCTID:722390006","UMLS:C3489725"],"synonyms":[{"name":"BLC-PMG","type":"exact"},{"name":"BLCPMG","type":"related"},{"name":"Baraitser Brett Piesowicz syndrome","type":"related"},{"name":"Baraitser-Brett-Piesowicz syndrome","type":"exact"},{"name":"Baraitser-Reardon syndrome","type":"exact"},{"name":"band-like calcification with simplified gyration and polymicrogyria","type":"exact"},{"name":"bilateral band-like calcification with polymicrogyria","type":"exact"},{"name":"congenital intrauterine infection-like syndrome","type":"related"},{"name":"microcephaly - intracranial calcification - intellectual disability","type":"related"},{"name":"microcephaly intracranial calcification","type":"related"},{"name":"microcephaly-intracranial calcification-intellectual disability syndrome","type":"exact"},{"name":"pseudo-TORCH syndrome","type":"exact"}],"termid":"MONDO:0009626","xrefs":{"Monarch":{"xref_id":"0009626"}}}


id: MONDO:0008893
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"C syndrome is a rare multiple congenital anomaly/intellectual disability syndrome characterized by trigonocephaly and metopic suture synostosis, dysmorphic facial features, short neck, skeletal anomalies, and variable intellectual disability.","definition_xrefs":["Orphanet:1308"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"C syndrome","secondary_identifiers":["GARD:5978","MEDGEN:167105","OMIM:211750","MESH:C537418","UMLS:C0796095","NORD:882","icd11.foundation:1482041278","DOID:0111581","SCTID:715409005"],"synonyms":[{"name":"C syndrome","type":"exact"},{"name":"OTCS","type":"exact"},{"name":"Opitz C trigonocephaly","type":"exact"},{"name":"Opitz trigonocephaly C syndrome","type":"exact"},{"name":"Opitz trigonocephaly syndrome","type":"exact"},{"name":"trigonocephaly C syndrome","type":"exact"},{"name":"trigonocephaly syndrome","type":"related"}],"termid":"MONDO:0008893","xrefs":{"Monarch":{"xref_id":"0008893"}}}


id: GO:0030027
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A thin sheetlike process extended by the leading edge of a migrating cell or extending cell process; contains a dense meshwork of actin filaments.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"},{"relation_name":"part_of","term_name":"cell leading edge","termid":"GO:0031252"}],"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":"lamellipodium","secondary_identifiers":["Wikipedia:Lamellipodia"],"termid":"GO:0030027"}


id: MONDO:0006216
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polypoid epithelial neoplasm that arises from the gallbladder. According to the neoplastic growth pattern, it is classified as tubular, tubulopapillary, or papillary.","definition_xrefs":["NCIT:C7720"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"biliary tract neoplasm","termid":"MONDO:0005304"},{"relation_name":"is_a","term_name":"digestive system adenoma","termid":"MONDO:0006180"},{"relation_name":"is_a","term_name":"gallbladder neoplasm","termid":"MONDO:0021253"},{"relation_name":"is_a","term_name":"polyp of gallbladder","termid":"MONDO:0021416"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"gallbladder adenoma","secondary_identifiers":["UMLS:C0238137","DOID:0050893","EFO:1000263","MEDGEN:116046"],"synonyms":[{"name":"adenoma of gallbladder","type":"exact"},{"name":"adenoma of the gallbladder","type":"exact"},{"name":"gall bladder adenoma","type":"exact"},{"name":"gallbladder adenoma","type":"exact"}],"termid":"MONDO:0006216","xrefs":{"Monarch":{"xref_id":"0006216"}}}


id: GO:1904888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a cranial skeletal system over time, from its formation to the mature structure. The cranial skeletal system is the skeletal subdivision of the head, and includes the skull (cranium plus mandible), pharyngeal and/or hyoid apparatus.","definition_xrefs":["GOC:PARL","PMID:11262227","GOC:bf","GOC:TermGenie","GO_REF:0000094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"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":"cranial skeletal system development","synonyms":[{"name":"cranial skeleton development","type":"narrow"},{"name":"craniofacial development","type":"narrow"},{"name":"cranium development","type":"related"},{"name":"osteocranium development","type":"narrow"}],"termid":"GO:1904888"}


id: MONDO:0018499
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"double outlet right ventricle","termid":"MONDO:0018089"}],"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":"double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy","secondary_identifiers":["GARD:21756","MEDGEN:1842277","Orphanet:423712","UMLS:C5680071"],"synonyms":[{"name":"DORV with atrioventricular septal defect, pulmonary stenosis, heterotaxy","type":"exact"}],"termid":"MONDO:0018499","xrefs":{"Monarch":{"xref_id":"0018499"}}}


id: MONDO:0020487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pontiac fever (PF) is a mild form of legionellosis manifesting with flu-like symptoms such as nausea, myalgia, fever, cough and headache but without pneumonia.","definition_xrefs":["Orphanet:99748"],"direct_ancestors":[{"relation_name":"is_a","term_name":"legionellosis","termid":"MONDO:0005823"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pontiac fever","secondary_identifiers":["NCIT:C128335","MedDRA:10054161","DOID:0050150","UMLS:C0343528","icd11.foundation:1670562980","GARD:13588","ICD9:041.89","MEDGEN:575661","SCTID:240447002"],"termid":"MONDO:0020487","xrefs":{"Monarch":{"xref_id":"0020487"}}}


id: PBO:0071024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 26","termid":"PBO:0071024"}


id: GO:0034518
data:
  {"annotated_genes":["SJAG_04360","SJAG_01954","SJAG_01830","SJAG_04772","SJAG_01064","SJAG_00507","SJAG_03223"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[76485,74153,75897,89283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016281"},{"annotations":[74994,117213,72117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005846"}]},"cv_name":"cellular_component","definition":"A protein complex that binds to an RNA cap structure to mediate RNA processing and/or translation initiation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00507":null,"SJAG_01064":null,"SJAG_01830":null,"SJAG_01954":null,"SJAG_03223":null,"SJAG_04360":null,"SJAG_04772":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"RNA cap binding complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0034518","terms_by_termid":{"GO:0005846":null,"GO:0016281":null}}


id: FYPO:0005979
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 actin filament bundle organization is abnormal. The process normally results in the assembly, arrangement of constituent parts, or disassembly of an actin filament bundle. Actin filament bundles are assemblies of actin filaments organized along a single axis.","definition_xrefs":["PomBase:mah","GO:0061572"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin filament organization during vegetative growth","termid":"FYPO:0000727"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"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:0004803","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal actin filament bundle organization","synonyms":[{"name":"abnormal actin filament bundle organisation during vegetative growth","type":"exact"},{"name":"abnormal actin filament bundle organization during mitotic cell cycle","type":"related"},{"name":"abnormal actin filament bundle organization during vegetative growth","type":"exact"}],"termid":"FYPO:0005979"}


id: MOD:01888
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes two neutral hydrogen atoms (proton and electron) from a residue.","definition_xrefs":["Unimod:401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dehydrogenated residue","termid":"MOD:00683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"didehydrogenated residue","synonyms":[{"name":"2dHRes","type":"exact"}],"termid":"MOD:01888"}


id: FYPO:0004476
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, occurs to a lower extent than normal during a cellular response to calcium ions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during vegetative growth","termid":"FYPO:0001838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0002494","FYPO:0002274"],"is_obsolete":false,"name":"decreased protein phosphorylation during cellular response to calcium ion","synonyms":[{"name":"decreased protein phosphorylation during cellular response to calcium","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to calcium ion during mitotic cell cycle","type":"related"},{"name":"decreased protein phosphorylation during cellular response to calcium ion during vegetative growth","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to calcium ion","type":"exact"}],"termid":"FYPO:0004476"}


id: GO:2000053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of Wnt signaling pathway involved in dorsal/ventral axis specification.","definition_xrefs":["GOC:yaf","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of Wnt signaling pathway involved in dorsal/ventral axis specification (obsolete GO:2000053)","synonyms":[{"name":"regulation of Wnt receptor signaling pathway involved in dorsal/ventral axis specification","type":"exact"},{"name":"regulation of Wnt receptor signalling pathway involved in dorsal/ventral axis specification","type":"exact"},{"name":"regulation of Wnt-activated signaling pathway involved in dorsal/ventral axis specification","type":"exact"}],"termid":"GO:2000053"}


id: GO:0070033
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains synaptobrevin 2 (VAMP2), SNAP-25, syntaxin 1a, and complexin II (or orthologs thereof).","definition_xrefs":["PMID:7553862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SNARE complex","termid":"GO:0031201"}],"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:0005737"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"synaptobrevin 2-SNAP-25-syntaxin-1a-complexin II complex","synonyms":[{"name":"SNARE complex (Vamp2, Snap25, Stx1a, Cplx2)","type":"narrow"},{"name":"Vamp2-Snap25-Stx1a-Cplx2 complex","type":"narrow"}],"termid":"GO:0070033"}


id: PBO:0044036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroitin sulfate proteoglycan 4 pseudogene 5","termid":"PBO:0044036"}


id: FYPO:0002185
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A mixed population phenotype in which all cells in a population are inviable, and the population includes a mixture of germinated spores and tapered vegetative cells. The tapered cells arise from division of some of the germinated spores, and may form a microcolony of up to 64 cells.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable mixed population including germinated spores and tapered cells (obsolete FYPO:0002185)","synonyms":[{"name":"inviable mixed population including germinated spores and bottle/skittle cells","type":"related"},{"name":"inviable mixed population including germinated spores and skittle-shaped cells","type":"exact"}],"termid":"FYPO:0002185"}


id: GO:0045088
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the innate immune response, the organism's first line of defense against infection.","definition_xrefs":["GOC:ebc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to biotic stimulus","termid":"GO:0002831"},{"relation_name":"is_a","term_name":"regulation of defense response","termid":"GO:0031347"},{"relation_name":"is_a","term_name":"regulation of response to external stimulus","termid":"GO:0032101"},{"relation_name":"is_a","term_name":"regulation of immune response","termid":"GO:0050776"},{"relation_name":"regulates","term_name":"innate immune response","termid":"GO:0045087"}],"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 innate immune response","termid":"GO:0045088"}


id: PR:P87312
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A crooked neck-like protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03851","PANTHER:PTHR11246:SF3","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":"pre-mRNA-splicing factor cwf4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC31F10.11c","secondary_identifiers":["UniProtKB:P87312"],"synonyms":[{"name":"Spom972h-CRNKL1","type":"exact"},{"name":"complexed with cdc5 protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87312"}


id: MONDO:0015976
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hyper-IgM syndrome without susceptibility to opportunistic infections (obsolete MONDO:0015976)","secondary_identifiers":["Orphanet:183666"],"synonyms":[{"name":"HIGM without susceptibility to opportunistic infections","type":"exact"}],"termid":"MONDO:0015976","xrefs":{"Monarch":{"xref_id":"0015976"}}}


id: SO:0000201
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An exon that is bounded by 5' and 3' splice sites.","definition_xrefs":["PMID:10373547"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exon","termid":"SO:0000147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interior_exon","synonyms":[{"name":"interior exon","type":"exact"}],"termid":"SO:0000201"}


id: GO:0048577
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces short-day photoperiodism, where the response associated with the photoperiodism is flowering. Flowering is defined by the switch from the vegetative to the reproductive phase.","definition_xrefs":["GOC:pj","ISBN:0582015952","ISBN:0709408862","ISBN:0697037754","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of post-embryonic development","termid":"GO:0048581"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of short-day photoperiodism, flowering","termid":"GO:0048587"},{"relation_name":"negatively_regulates","term_name":"short-day photoperiodism, flowering","termid":"GO:0048575"}],"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 short-day photoperiodism, flowering","synonyms":[{"name":"down regulation of short-day photoperiodism, flowering","type":"exact"},{"name":"down-regulation of short-day photoperiodism, flowering","type":"exact"},{"name":"downregulation of short-day photoperiodism, flowering","type":"exact"},{"name":"inhibition of short-day photoperiodism, flowering","type":"narrow"}],"termid":"GO:0048577"}


id: PBO:0042084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 150 pseudogene 1","termid":"PBO:0042084"}


id: GO:0007075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase III promoter as the cell leaves M phase. M phase is the part of the mitotic cell cycle during which mitosis and cytokinesis take place.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription involved in exit from mitosis, from RNA polymerase III promoter (obsolete GO:0007075)","synonyms":[{"name":"activation of transcription on exit from mitosis, from Pol III promoter","type":"narrow"},{"name":"activation of transcription on exit from mitosis, from RNA polymerase III promoter","type":"narrow"}],"termid":"GO:0007075"}


id: PBO:0070108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 22 pseudogene","termid":"PBO:0070108"}


id: GO:1901207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of heart looping.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of morphogenesis of an epithelium","termid":"GO:1905330"},{"relation_name":"regulates","term_name":"heart looping","termid":"GO:0001947"}],"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 heart looping","synonyms":[{"name":"regulation of cardiac looping","type":"exact"}],"termid":"GO:1901207"}


id: GO:0021759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the globus pallidus over time from its initial formation until its mature state. The globus pallidus is one of the basal ganglia involved with control of voluntary movement in the brain.","definition_xrefs":["GOC:jid","ISBN:0878937420","GOC:dph","GOC:cls","GOC:dgh","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"diencephalon development","termid":"GO:0021536"}],"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":"globus pallidus development","synonyms":[{"name":"pallidum development","type":"exact"}],"termid":"GO:0021759"}


id: PBO:0085827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; gene expression increases in cultures shifted to a lower temperature; protein abundance increases in response to DNA replication stress","termid":"PBO:0085827"}


id: GO:0018450
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: myrtenol + O2 + 2 H+ + 2 e- = 2 H2O + myrtenal.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete myrtenol dehydrogenase activity (obsolete GO:0018450)","termid":"GO:0018450"}


id: GO:2000525
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of T cell costimulation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of T cell activation","termid":"GO:0050870"},{"relation_name":"is_a","term_name":"regulation of T cell costimulation","termid":"GO:2000523"},{"relation_name":"positively_regulates","term_name":"T cell costimulation","termid":"GO:0031295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"positively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"positive regulation of T cell costimulation","synonyms":[{"name":"positive regulation of T cell co-stimulation","type":"exact"},{"name":"positive regulation of T lymphocyte costimulation","type":"exact"},{"name":"positive regulation of T-cell co-stimulation","type":"exact"},{"name":"positive regulation of T-cell costimulation","type":"exact"},{"name":"positive regulation of T-lymphocyte costimulation","type":"exact"}],"termid":"GO:2000525"}


id: PBO:0034288
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-indirectly_inhibits","termid":"PBO:0034288"}


id: PBO:0044056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystatin SA pseudogene 1","termid":"PBO:0044056"}


id: GO:0097291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A renal system process in which phosphate ions are taken up from the collecting ducts and proximal and distal loops of the nephron. In non-mammalian species, absorption may occur in related structures.","definition_xrefs":["PMID:18784102","GOC:lb","PMID:22506049"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal absorption","termid":"GO:0070293"}],"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":"renal phosphate ion absorption","synonyms":[{"name":"renal phosphate absorption","type":"exact"}],"termid":"GO:0097291"}


id: GO:0140431
data:
  {"annotated_genes":["SJAG_05257"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108879],"is_not":false,"summary":null,"term":"GO:0140431"}]},"cv_name":"molecular_function","definition":"Binding to a DNA site that has neither a purine nor a pyrimidine base. Apurinic sites can form spontaneously or when DNA glycosylase removes a damaged base.","definition_xrefs":["PMID:23245849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"damaged DNA binding","termid":"GO:0003684"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05257":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0003677"],"is_obsolete":false,"name":"DNA-(abasic site) binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA AP site binding","type":"exact"},{"name":"DNA-(apurinic site) binding","type":"narrow"},{"name":"DNA-(apurinic site/apyrimidinic site) binding","type":"exact"},{"name":"DNA-(apyrimidinic site) binding","type":"narrow"}],"termid":"GO:0140431","terms_by_termid":{"GO:0140431":null}}


id: PBO:0045146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal heavy chain 3","termid":"PBO:0045146"}


id: PBO:0075543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm antigen with calponin homology and coiled-coil domains 1","termid":"PBO:0075543"}


id: PBO:0089814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-2 adaptor complex sigma subunit Aps2","termid":"PBO:0089814"}


id: MONDO:0008076
data:
  {"annotated_genes":["SJAG_00663"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87901],"is_not":false,"summary":null,"term":"MONDO:0008076"}]},"cv_name":"mondo","definition":"An autosomal dominant form of recurrent focal neuropathy characterized clinically by acute, recurrent episodes of brachial plexus neuropathy with muscle weakness and atrophy preceded by severe pain in the affected arm.","definition_xrefs":["OMIM:162100"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"neuralgic amyotrophy","termid":"MONDO:0017362"},{"relation_name":"is_a","term_name":"brachial plexus neuropathy","termid":"MONDO:0006683"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00663":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"amyotrophic neuralgia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:353.5","SCTID:26609002","DOID:10383","GARD:3955","MESH:D020968","UMLS:C1834304","MEDGEN:320318"],"synonyms":[{"name":"HNA","type":"related"},{"name":"amyotrophy, hereditary neuralgic","type":"exact"},{"name":"amyotrophy, hereditary neuralgic, with predilection for brachial plexus","type":"exact"},{"name":"brachial plexus neuropathy, hereditary","type":"exact"},{"name":"hereditary brachial plexus neuropathy","type":"exact"},{"name":"hereditary neuralgic amyotrophy","type":"exact"},{"name":"neuralgic amyotrophy","type":"related"},{"name":"neuritis with brachial predilection","type":"exact"}],"termid":"MONDO:0008076","terms_by_termid":{"MONDO:0008076":null},"xrefs":{"Monarch":{"xref_id":"0008076"}}}


id: MONDO:0003826
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extragonadal malignant germ cell tumor that arises from the mediastinum. It is characterized by the presence of uniform cells with clear or eosinophilic cytoplasm, round nucleus with one or more nucleoli, and distinct cellular borders. It usually arises from the anterior mediastinum. It may present with respiratory distress, chest pain, or superior vena cava syndrome or it may be asymptomatic, with the tumor detected on routine chest x-ray. The prognosis of mediastinal pure seminomas is favorable compared to the mediastinal non-seminomatous malignant germ cell tumors.","definition_xrefs":["NCIT:C6812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extragonadal seminoma","termid":"MONDO:0003668"},{"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":"mediastinum seminoma","secondary_identifiers":["MEDGEN:277355","DOID:6249","UMLS:C1334680"],"synonyms":[{"name":"mediastinal seminoma","type":"exact"},{"name":"mediastinum seminoma","type":"exact"},{"name":"seminoma of mediastinum","type":"exact"},{"name":"seminoma of the mediastinum","type":"exact"}],"termid":"MONDO:0003826","xrefs":{"Monarch":{"xref_id":"0003826"}}}


id: MONDO:0020708
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurodegenerative condition characterized by asymmetric weakness in the upper extremities resulting from segmental lower motor neuron dysfunction.","definition_xrefs":["NCIT:C133085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"brachial amyotrophic diplegia","secondary_identifiers":["MEDGEN:1617621","UMLS:C4522181"],"synonyms":[{"name":"BAD","type":"broad"},{"name":"FAS","type":"exact"},{"name":"brachial amyotrophic diplegia","type":"exact"},{"name":"flail arm syndrome","type":"exact"},{"name":"man-in-barrel syndrome","type":"exact"}],"termid":"MONDO:0020708","xrefs":{"Monarch":{"xref_id":"0020708"}}}


id: PBO:0059298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L47","termid":"PBO:0059298"}


id: PBO:0059761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 35","termid":"PBO:0059761"}


id: GO:0008041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete storage protein of fat body (sensu Insecta) (obsolete GO:0008041)","synonyms":[{"name":"storage protein of fat body (sensu Insecta)","type":"exact"}],"termid":"GO:0008041"}


id: PBO:0032719
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_level_during_mitotic_metaphase","termid":"PBO:0032719"}


id: PBO:0054048
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 1389","termid":"PBO:0054048"}


id: GO:0045612
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hemocyte differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune system process","termid":"GO:0002684"},{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of hemocyte differentiation","termid":"GO:0045610"},{"relation_name":"positively_regulates","term_name":"hemocyte differentiation","termid":"GO:0042386"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of hemocyte differentiation","synonyms":[{"name":"activation of hemocyte differentiation","type":"narrow"},{"name":"positive regulation of arthropod blood cell differentiation","type":"exact"},{"name":"stimulation of hemocyte differentiation","type":"narrow"},{"name":"up regulation of hemocyte differentiation","type":"exact"},{"name":"up-regulation of hemocyte differentiation","type":"exact"},{"name":"upregulation of hemocyte differentiation","type":"exact"}],"termid":"GO:0045612"}


id: PBO:0079486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin domain containing 2","termid":"PBO:0079486"}


id: GO:0060698
data:
  {"annotated_genes":["SJAG_02594"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90605],"is_not":false,"summary":null,"term":"GO:0060698"}]},"cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of endoribonuclease.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonuclease inhibitor activity","termid":"GO:0008428"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02594":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0140678","GO:0004857","GO:0098772","GO:0003674","GO:0030234"],"is_obsolete":false,"name":"endoribonuclease inhibitor activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0060698","terms_by_termid":{"GO:0060698":null}}


id: PBO:0064497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit A","termid":"PBO:0064497"}


id: MONDO:0010218
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46,XX testicular disorder of sex development","termid":"MONDO:0100249"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"46,XX sex reversal 2","secondary_identifiers":["OMIM:278850","GARD:15249","MEDGEN:411414","UMLS:C2749215","DOID:0111763"],"synonyms":[{"name":"46,XX SEX reversal 2","type":"related"},{"name":"46,XX Sex reversal type 2","type":"exact"},{"name":"46,XX sex reversal 2","type":"exact"},{"name":"46XX sex reversal 2","type":"exact"},{"name":"SRXX2","type":"related"},{"name":"chromosome 17Q24 Duplication syndrome","type":"related"}],"termid":"MONDO:0010218","xrefs":{"Monarch":{"xref_id":"0010218"}}}


id: MONDO:0037821
data:
  {"annotated_genes":["SJAG_05283","SJAG_03785","SJAG_05213","SJAG_02876","SJAG_03363","SJAG_03961","SJAG_02896","SJAG_04109","SJAG_01372","SJAG_00938","SJAG_04944","SJAG_05194","SJAG_01344","SJAG_01841","SJAG_03011"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008294"},{"annotations":[88277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008822"},{"annotations":[88537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011559"},{"annotations":[88736,88735],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030810"},{"annotations":[87612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031040"},{"annotations":[87195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009902"},{"annotations":[87039,87040,87041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009380"},{"annotations":[87451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008296"},{"annotations":[87150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030048"},{"annotations":[87604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007369"},{"annotations":[87196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013000"},{"annotations":[88667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011156"},{"annotations":[87277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011214"},{"annotations":[86887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008319"},{"annotations":[87470],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008297"},{"annotations":[88123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957577"},{"annotations":[88467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010420"},{"annotations":[88465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020721"}]},"cv_name":"mondo","definition":"A disease that has its basis in the disruption of porphyrin-containing compound metabolic process.","definition_xrefs":["MONDO:patterns/basis_in_disruption_of_process"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_01344":null,"SJAG_01372":null,"SJAG_01841":null,"SJAG_02876":null,"SJAG_02896":null,"SJAG_03011":null,"SJAG_03363":null,"SJAG_03785":null,"SJAG_03961":null,"SJAG_04109":null,"SJAG_04944":null,"SJAG_05194":null,"SJAG_05213":null,"SJAG_05283":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"porphyrin metabolism disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:277.1","MEDGEN:10865","SCTID:29094004","UMLS:C0032708"],"synonyms":[{"name":"disorder of porphyrin and heme metabolism","type":"related"},{"name":"disorder of porphyrin metabolism","type":"exact"},{"name":"disorder of porphyrin-containing compound metabolic process","type":"exact"},{"name":"porphyrin-containing compound metabolic process disease","type":"exact"}],"termid":"MONDO:0037821","terms_by_termid":{"MONDO:0007369":null,"MONDO:0008294":null,"MONDO:0008296":null,"MONDO:0008297":null,"MONDO:0008319":null,"MONDO:0008822":null,"MONDO:0009380":null,"MONDO:0009902":null,"MONDO:0010420":null,"MONDO:0011156":null,"MONDO:0011214":null,"MONDO:0011559":null,"MONDO:0013000":null,"MONDO:0020721":null,"MONDO:0030048":null,"MONDO:0030810":null,"MONDO:0031040":null,"MONDO:0957577":null},"xrefs":{"Monarch":{"xref_id":"0037821"}}}


id: MONDO:0013620
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the SCN4A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"postsynaptic congenital myasthenic syndrome","termid":"MONDO:0020344"},{"relation_name":"is_a","term_name":"SCN4A-related myopathy, autosomal recessive","termid":"MONDO:0100121"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0006025","MONDO:0002320"],"is_obsolete":false,"name":"congenital myasthenic syndrome 16","secondary_identifiers":["GARD:15771","DOID:0110682","MEDGEN:481742","OMIM:614198","UMLS:C3280112"],"synonyms":[{"name":"CMS16","type":"exact"},{"name":"SCN4A congenital myasthenic syndrome","type":"exact"},{"name":"congenital myasthenic syndrome acetazolamide-responsive","type":"exact"},{"name":"congenital myasthenic syndrome caused by mutation in SCN4A","type":"exact"},{"name":"congenital myasthenic syndrome type 16","type":"exact"},{"name":"myasthenic syndrome, congenital, 16","type":"related"},{"name":"myasthenic syndrome, congenital, Acetazolamide-responsive","type":"related"},{"name":"myasthenic syndrome, congenital, type 16","type":"exact"}],"termid":"MONDO:0013620","xrefs":{"Monarch":{"xref_id":"0013620"}}}


id: FYPO:0006413
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 one or more histone RNAs measured in a cell is higher than normal (i.e. lower than observed in wild-type cells). Histone RNAs are transcribed from genes encoding histones.","definition_xrefs":["PomBase:mah","PMID:17452352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased level of histone gene mRNA during vegetative growth","synonyms":[{"name":"increased histone gene mRNA accumulation during vegetative growth","type":"related"},{"name":"increased level of histone gene RNA during vegetative growth","type":"exact"},{"name":"increased level of histone gene mRNA during mitotic cell cycle","type":"related"},{"name":"increased level of histone gene transcripts during vegetative growth","type":"exact"}],"termid":"FYPO:0006413"}


id: MONDO:0002786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer involving a diencephalon.","definition_xrefs":["MONDO:patterns/cancer"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supratentorial cancer","termid":"MONDO:0002071"}],"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":"diencephalic cancer","secondary_identifiers":["NCIT:C5126","DOID:3843","MEDGEN:233659","UMLS:C1334576"],"synonyms":[{"name":"cancer of diencephalon","type":"exact"},{"name":"diencephalic neoplasm","type":"related"},{"name":"diencephalon cancer","type":"exact"},{"name":"malignant diencephalic neoplasm","type":"exact"},{"name":"malignant diencephalic neoplasms","type":"exact"},{"name":"malignant diencephalic tumor","type":"exact"},{"name":"malignant diencephalic tumour","type":"exact"},{"name":"malignant diencephalon neoplasm","type":"exact"},{"name":"malignant neoplasm of diencephalon","type":"exact"},{"name":"tumor of diencephalon","type":"exact"},{"name":"tumour of diencephalon","type":"exact"}],"termid":"MONDO:0002786","xrefs":{"Monarch":{"xref_id":"0002786"}}}


id: PBO:0009146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium-dependent serine/threonine protein phosphatase calcineurin A, catalytic subunit Ppb1","termid":"PBO:0009146"}


id: internal:broad
data:
  {"annotation_feature_type":"gene","cv_name":"synonym_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"broad","termid":"internal:broad"}


id: GO:0032388
data:
  {"annotated_genes":["SJAG_03048","SJAG_01245","SJAG_04597","SJAG_02592","SJAG_01805","SJAG_04464","SJAG_03453","SJAG_04312"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902854"},{"annotations":[103647,95582,112844,102228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046827"},{"annotations":[96147,92618,104182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042307"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the directed movement of substances within cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular transport","termid":"GO:0032386"},{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of transport","termid":"GO:0051050"},{"relation_name":"positively_regulates","term_name":"intracellular transport","termid":"GO:0046907"}],"gene_count":8,"genes_by_uniquename":{"SJAG_01245":null,"SJAG_01805":null,"SJAG_02592":null,"SJAG_03048":null,"SJAG_03453":null,"SJAG_04312":null,"SJAG_04464":null,"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of intracellular transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of intracellular transport","type":"narrow"},{"name":"stimulation of intracellular transport","type":"narrow"},{"name":"up regulation of intracellular transport","type":"exact"},{"name":"up-regulation of intracellular transport","type":"exact"},{"name":"upregulation of intracellular transport","type":"exact"}],"termid":"GO:0032388","terms_by_termid":{"GO:0042307":null,"GO:0046827":null,"GO:1902854":null}}


id: PBO:0070449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L3 pseudogene 6","termid":"PBO:0070449"}


id: PBO:0060143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myotrophin","termid":"PBO:0060143"}


id: PBO:0036339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"claspin, Mrc1","termid":"PBO:0036339"}


id: GO:0048236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of plant spores derived from the products of meiosis. The spore gives rise to gametophytes.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sexual sporulation","termid":"GO:0034293"},{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"},{"relation_name":"is_a","term_name":"meiotic cell cycle","termid":"GO:0051321"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"plant-type sporogenesis","synonyms":[{"name":"plant spore formation","type":"exact"}],"termid":"GO:0048236"}


id: MONDO:0023267
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":"goldstein hutt syndrome","secondary_identifiers":["MEDGEN:419084","UMLS:C2931465","MESH:C537282"],"synonyms":[{"name":"long eyelashes, cataract, and hereditary spherocytosis","type":"related"},{"name":"trichomegaly, cataract, and hereditary spherocytosis","type":"related"}],"termid":"MONDO:0023267","xrefs":{"Monarch":{"xref_id":"0023267"}}}


id: FYPO:0007245
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the meiotic spindle pole bodies are normal (i.e. indistinguishable from wild type) with respect to structure, composition, location, and orientation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal spindle pole body","termid":"FYPO:0005379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal meiotic spindle pole body","synonyms":[{"name":"normal meiotic SPB","type":"exact"},{"name":"normal spindle pole body during meiotic cell cycle","type":"exact"}],"termid":"FYPO:0007245"}


id: GO:0090549
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a starvation stimulus, deprivation of a carbon source.","definition_xrefs":["GOC:tair_curators","PMID:18245858"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to starvation","termid":"GO:0042594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to carbon starvation","termid":"GO:0090549"}


id: PBO:0003847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Sof1 (predicted)","termid":"PBO:0003847"}


id: PBO:0002990
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae CAN1","termid":"PBO:0002990"}


id: PBO:0091901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scizosaccharomyces pombe specific protein","termid":"PBO:0091901"}


id: GO:1901002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of response to salt stress.","definition_xrefs":["PMID:22627139","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"is_a","term_name":"regulation of response to salt stress","termid":"GO:1901000"},{"relation_name":"positively_regulates","term_name":"response to salt stress","termid":"GO:0009651"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of response to salt stress","synonyms":[{"name":"activation of response to ionic osmotic stress","type":"exact"},{"name":"activation of response to salt stress","type":"narrow"},{"name":"activation of salinity response","type":"exact"},{"name":"positive regulation of response to ionic osmotic stress","type":"exact"},{"name":"positive regulation of salinity response","type":"exact"},{"name":"up regulation of response to ionic osmotic stress","type":"exact"},{"name":"up regulation of response to salt stress","type":"exact"},{"name":"up regulation of salinity response","type":"exact"},{"name":"up-regulation of response to ionic osmotic stress","type":"exact"},{"name":"up-regulation of response to salt stress","type":"exact"},{"name":"up-regulation of salinity response","type":"exact"},{"name":"upregulation of response to ionic osmotic stress","type":"exact"},{"name":"upregulation of response to salt stress","type":"exact"},{"name":"upregulation of salinity response","type":"exact"}],"termid":"GO:1901002"}


id: PBO:0044034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CSPG4 pseudogene 3 Y-linked","termid":"PBO:0044034"}


id: PBO:0012847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptide-methionine (R)-S-oxide reductase MsrB","termid":"PBO:0012847"}


id: PBO:0089801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S11","termid":"PBO:0089801"}


id: FYPO:0001479
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of alpha,alpha-trehalase 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:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"abnormal alpha,alpha-trehalase activity","synonyms":[{"name":"abnormal neutral trehalase activity","type":"exact"},{"name":"abnormal trehalase activity","type":"broad"}],"termid":"FYPO:0001479"}


id: MONDO:1010076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypereosinophilic syndrome that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"},{"relation_name":"is_a","term_name":"cardiomyopathy, non-human animal","termid":"MONDO:1010010"},{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"},{"relation_name":"is_a","term_name":"syndromic disease, non-human animal","termid":"MONDO:1011360"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypereosinophilic syndrome, non-human animal","secondary_identifiers":["OMIA:000502"],"termid":"MONDO:1010076","xrefs":{"Monarch":{"xref_id":"1010076"}}}


id: GO:0060126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized structural and/or functional features of a somatotropin secreting cell. A somatotropin secreting cell is an acidophilic cell of the anterior pituitary that produces growth hormone, somatotropin.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"adenohypophysis development","termid":"GO:0021984"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"somatotropin secreting cell differentiation","synonyms":[{"name":"growth hormone secreting cell differentiation","type":"exact"},{"name":"somatotrope differentiation","type":"related"},{"name":"somatotroph differentiation","type":"related"},{"name":"somatotrophin secreting cell differentiation","type":"exact"},{"name":"somatotropic cell differentiation","type":"related"},{"name":"somatrophic cell differentiation","type":"related"}],"termid":"GO:0060126"}


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


id: GO:0009615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus from a virus.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to other organism","termid":"GO:0051707"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to virus","secondary_identifiers":["Reactome:R-HSA-9824446"],"synonyms":[{"name":"response to viruses","type":"exact"}],"termid":"GO:0009615"}


id: PBO:0050968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon omega 1 pseudogene 2","termid":"PBO:0050968"}


id: PBO:0088058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-protein ligase; involved in proteasome-dependent degradation of aberrant nuclear proteins; targets substrates with regions of exposed hydrophobicity containing 5 or more contiguous hydrophobic residues; contains intrinsically disordered regions that contribute to substrate recognition; prefers a window of exposed hydrophobicity that causes a particular level of protein insolubility, suggesting that San1p evolved to target highly aggregation-prone proteins","termid":"PBO:0088058"}


id: PBO:0078964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ser (anticodon AGA) 3-1","termid":"PBO:0078964"}


id: MONDO:0000903
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myoclonus-dystonia syndrome (MDS) is a rare movement disorder characterized by mild to moderate dystonia along with 'lightning-like' myoclonic jerks.","definition_xrefs":["Orphanet:36899"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined dystonia","termid":"MONDO:0020065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"myoclonus-dystonia syndrome","secondary_identifiers":["NANDO:1200522","GARD:7139","ICD9:333.99","DOID:0090033","SCTID:439732004","MESH:C536096"],"synonyms":[{"name":"DYT-SGCE","type":"exact"},{"name":"DYT11","type":"related"},{"name":"Hereditary essential myoclonus","type":"related"},{"name":"alcohol-responsive dystonia","type":"related"},{"name":"dystonia 11","type":"related"},{"name":"dystonia 11, myoclonic","type":"related"},{"name":"dystonia with myoclonus","type":"exact"},{"name":"dystonia, alcohol responsive","type":"related"},{"name":"dystonia, alcohol-responsive","type":"related"},{"name":"dystonia-11, myoclonic","type":"related"},{"name":"hereditary essential myoclonus","type":"exact"},{"name":"myoclonic dystonia","type":"exact"},{"name":"myoclonus, hereditary essential","type":"related"},{"name":"myoclonus-Dystonia","type":"related"},{"name":"myoclonus-dystonia","type":"related"},{"name":"myoclonus-dystonia syndrome","type":"exact"}],"termid":"MONDO:0000903","xrefs":{"Monarch":{"xref_id":"0000903"}}}


id: GO:0034725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The controlled breakdown of nucleosomes on newly replicated DNA, coupled to strand elongation.","definition_xrefs":["GOC:mah","PMID:17510629"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA replication-dependent nucleosome disassembly (obsolete GO:0034725)","synonyms":[{"name":"DNA replication-dependent chromatin disassembly","type":"exact"}],"termid":"GO:0034725"}


id: PBO:0062650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 13 subfamily A member 1","termid":"PBO:0062650"}


id: GO:0008300
data:
  {"annotated_genes":["SJAG_04954"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016095"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of an isoprenoid compound, isoprene (2-methylbuta-1,3-diene) or compounds containing or derived from linked isoprene (3-methyl-2-butenylene) residues.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid metabolic process","termid":"GO:0006720"},{"relation_name":"is_a","term_name":"lipid catabolic process","termid":"GO:0016042"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04954":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"isoprenoid catabolic process","references_by_uniquename":{"GO_REF:0000104":null},"secondary_identifiers":["GO:0016097"],"synonyms":[{"name":"isoprenoid breakdown","type":"exact"},{"name":"isoprenoid catabolism","type":"exact"},{"name":"isoprenoid degradation","type":"exact"},{"name":"polyisoprenoid breakdown","type":"narrow"},{"name":"polyisoprenoid catabolic process","type":"narrow"},{"name":"polyisoprenoid catabolism","type":"narrow"},{"name":"polyisoprenoid degradation","type":"narrow"},{"name":"polyterpene catabolic process","type":"narrow"},{"name":"polyterpene catabolism","type":"narrow"}],"termid":"GO:0008300","terms_by_termid":{"GO:0016095":null}}


id: GO:0141024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a symbiont to its host by binding to a carbohydrate on the host cell surface. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:15210807","PMID:19527885","PMID:30736336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adhesion of symbiont to host cell","termid":"GO:0044650"}],"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":"adhesion of symbiont to host cell surface via host membrane carbohydrate","termid":"GO:0141024"}


id: PBO:0043405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CKLF like MARVEL transmembrane domain containing 2","termid":"PBO:0043405"}


id: GO:0018166
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The ATP-dependent addition of a tyrosine residue to the C-terminus of a protein; typically the addition of tyrosine to the C-terminus of detyrosinated alpha-tubulin by the enzyme tubulin-tyrosine ligase.","definition_xrefs":["RESID:AA0257"],"gene_count":0,"genotype_count":0,"name":"obsolete C-terminal protein-tyrosinylation (obsolete GO:0018166)","termid":"GO:0018166"}


id: FYECO:0000417
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in medium containing glucose (typically <2% w/v), salts, water and with L-glutamatic acid as the nitrogen source.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucose MM, methionine nitrogen source","synonyms":[{"name":"glucose minimal medium, methionine nitrogen source","type":"exact"},{"name":"standard glucose minimal medium, methionine nitrogen source","type":"related"}],"termid":"FYECO:0000417"}


id: MONDO:0014530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency is a rare, genetic, slowly progressive neurodegenerative disease resulting from GRID2 deficiency characterized by motor, speech and cognitive delay, hypotonia, truncal and appendicular ataxia, and eye movement abnormalities (tonic upgaze, nystagmus, oculomotor apraxia). Intention tremor may also be associated. Brain imaging reveals progressive cerebellar atrophy with cerebellar flocculus particularly affected.","definition_xrefs":["Orphanet:363432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome","termid":"MONDO:0018189"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"autosomal recessive spinocerebellar ataxia 18","secondary_identifiers":["MEDGEN:863942","DOID:0080042","GARD:17557","UMLS:C4015505","OMIM:616204"],"synonyms":[{"name":"GRID2 autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome","type":"exact"},{"name":"GRID2 autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome","type":"exact"},{"name":"SCAR18","type":"exact"},{"name":"autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome caused by mutation in GRID2","type":"exact"},{"name":"autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome caused by mutation in GRID2","type":"exact"},{"name":"autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency","type":"related"},{"name":"autosomal recessive congenital cerebellar ataxia due to ionotropic glutamate receptor delta-2 subunit deficiency","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia type 18","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 18","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive type 18","type":"exact"}],"termid":"MONDO:0014530","xrefs":{"Monarch":{"xref_id":"0014530"}}}


id: PBO:0088536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AAA family ATPase Gcn20","termid":"PBO:0088536"}


id: PBO:0053020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LanC like glutathione S-transferase 1","termid":"PBO:0053020"}


id: PBO:0057233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 412","termid":"PBO:0057233"}


id: MONDO:0008260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB), besides simplex, junctional and dystrophic forms, and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes.","definition_xrefs":["Orphanet:2908"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited epidermolysis bullosa","termid":"MONDO:0019276"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"Kindler syndrome","secondary_identifiers":["DOID:0060472","GARD:4391","MEDGEN:96060","NANDO:1200239","OMIM:173650","SCTID:238836000","icd11.foundation:726317303","MESH:C536321","UMLS:C0406557"],"synonyms":[{"name":"KINDLER syndrome","type":"related"},{"name":"KNDLRS","type":"related"},{"name":"KS","type":"exact"},{"name":"Kindler syndrome","type":"exact"},{"name":"bullous acrokeratotic poikiloderma of Kindler and Weary","type":"related"},{"name":"congenital bullous poikiloderma","type":"related"},{"name":"poikiloderma of Kindler","type":"exact"},{"name":"poikiloderma, congenital, with bullae, Weary type","type":"related"},{"name":"poikiloderma, hereditary acrokeratotic","type":"related"}],"termid":"MONDO:0008260","xrefs":{"Monarch":{"xref_id":"0008260"}}}


id: PBO:0072319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 5","termid":"PBO:0072319"}


id: PBO:0001730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA snR101","termid":"PBO:0001730"}


id: PBO:0025541
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae VAM7","termid":"PBO:0025541"}


id: PBO:0075167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein D2 pseudogene 1","termid":"PBO:0075167"}


id: MONDO:0032933
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"partial duplication of the short arm of chromosome 1","termid":"MONDO:0017012"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant","secondary_identifiers":["DOID:0070470","OMIM:618815","MEDGEN:1708515","Orphanet:656279","UMLS:C5394150"],"synonyms":[{"name":"CHROMOSOME 1p36.33 DUPLICATION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL DOMINANT","type":"related"}],"termid":"MONDO:0032933","xrefs":{"Monarch":{"xref_id":"0032933"}}}


id: GO:0097292
data:
  {"annotated_genes":["SJAG_01298","SJAG_06634"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110090,77326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving XMP, xanthosine monophosphate.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"purine ribonucleoside monophosphate metabolic process","termid":"GO:0009167"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01298":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"XMP metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"XMP metabolism","type":"exact"}],"termid":"GO:0097292","terms_by_termid":{"GO:0032265":null}}


id: MONDO:0030995
data:
  {"annotated_genes":["SJAG_03042"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87306],"is_not":false,"summary":null,"term":"MONDO:0030995"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03042":null},"genotype_count":0,"is_obsolete":false,"name":"global developmental delay with speech and behavioral abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619243","GARD:18541","UMLS:C5543226","MEDGEN:1787991"],"synonyms":[{"name":"GDSBA","type":"exact"}],"termid":"MONDO:0030995","terms_by_termid":{"MONDO:0030995":null},"xrefs":{"Monarch":{"xref_id":"0030995"}}}


id: PATO:0002046
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's being away from or on the opposite side of the central axis.","definition_xrefs":["medical-dictionary:http://medical-dictionary.thefreedictionary.com/abaxial"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abaxial to","termid":"PATO:0002046"}


id: PR:P25457
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 60S ribosomal protein L7 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01432","PANTHER:PTHR11524:SF5","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":"60S ribosomal protein L7-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3H5.07","secondary_identifiers":["UniProtKB:P25457"],"synonyms":[{"name":"Spom972h-RPL7","type":"exact"}],"termid":"PR:P25457"}


id: GO:0042444
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phenylethylamine, an amine with pharmacological properties similar to those of amphetamine, occurs naturally as a neurotransmitter in the brain, and is present in chocolate and oil of bitter almonds.","definition_xrefs":["GOC:jl","ISBN:0395825172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biogenic amine biosynthetic process","termid":"GO:0042401"},{"relation_name":"is_a","term_name":"phenylethylamine metabolic process","termid":"GO:0042443"},{"relation_name":"is_a","term_name":"primary amino compound biosynthetic process","termid":"GO:1901162"}],"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":"phenylethylamine biosynthetic process","synonyms":[{"name":"phenylethylamine anabolism","type":"exact"},{"name":"phenylethylamine biosynthesis","type":"exact"},{"name":"phenylethylamine formation","type":"exact"},{"name":"phenylethylamine synthesis","type":"exact"}],"termid":"GO:0042444"}


id: PBO:0053624
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 667","termid":"PBO:0053624"}


id: GO:0016493
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a C-C chemokine and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity. C-C chemokines do not have an amino acid between the first two cysteines of the characteristic four-cysteine motif.","definition_xrefs":["GOC:signaling","PMID:8662823"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine receptor activity","termid":"GO:0004950"}],"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":"C-C chemokine receptor activity","termid":"GO:0016493"}


id: PBO:0061000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NHP2 ribonucleoprotein","termid":"PBO:0061000"}


id: MONDO:0006553
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic skin disease most common in women aged 13-35 years.It is characterized by the development of intense itching in the underarm area, the pubic area, and around the nipple of the breast as a result of perspiration which becomes trapped in the sweat gland and surrounding areas. The cause is unknown, but heat, humidity, and stress may play a role. Treatment may include the use of retinoids, antibiotics, and immunosuppressants.","direct_ancestors":[{"relation_name":"is_a","term_name":"sweat gland disorder","termid":"MONDO:0006615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"Fox-Fordyce disease","secondary_identifiers":["NCIT:C84716","DOID:1381","SCTID:65038009","ICD10CM:L75.2","UMLS:C0016632","MEDGEN:42092","Wikipedia:Fox-Fordyce_disease","ICD9:705.82","MESH:D005588"],"synonyms":[{"name":"Fox Fordyce disease","type":"exact"},{"name":"Fox-Fordyce disease","type":"exact"},{"name":"Fox-Fordyce syndrome","type":"related"},{"name":"apocrine miliaria","type":"related"},{"name":"miliaria, apocrine","type":"related"}],"termid":"MONDO:0006553","xrefs":{"Monarch":{"xref_id":"0006553"}}}


id: GO:0090143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the nucleoid. The nucleoid is the region of a bacterial cell, virion, mitochondrion or chloroplast to which the DNA is confined.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ascb_2009"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleoid organization (obsolete GO:0090143)","synonyms":[{"name":"nucleoid organisation","type":"exact"}],"termid":"GO:0090143"}


id: RO:0002388
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x has potential to directly develop into y iff x directly develops into y or x is capable of directly developing into y","direct_ancestors":[{"relation_name":"is_a","term_name":"has_potential_to_develop_into","termid":"RO:0002387"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_potential_to_directly_develop_into","termid":"RO:0002388"}


id: PBO:0064758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase C","termid":"PBO:0064758"}


id: FYPO:0007784
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to protein aggregate centers is decreased. Protein aggregate centers are composed of chaperones and misfolded proteins, and are reversibly formed in the nucleus and cytosol to shield thermosensitive proteins from degradation until conditions allow disaggregation and refolding.","definition_xrefs":["PomBase:mah","PMID:33946513","PMID:32075773"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein localization to protein aggregate center","synonyms":[{"name":"decreased protein localisation to protein aggregate centre","type":"exact"},{"name":"decreased protein localization to PAC","type":"exact"},{"name":"decreased protein localization to PACs","type":"exact"},{"name":"decreased protein localization to protein aggregate center during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to protein aggregate center during vegetative growth","type":"exact"},{"name":"reduced protein localization to protein aggregate center","type":"exact"}],"termid":"FYPO:0007784"}


id: GO:0102312
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-coumaryl-CoA + 2-oxoglutarate + O2 = 2,4-dihydroxycinnamoyl-CoA + succinate + carbon dioxide.","definition_xrefs":["PMID:22168819","PMID:22169019","GOC:pz"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"4-coumaroyl 2'-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-12963","RHEA:57868","EC:1.14.11.62"],"termid":"GO:0102312"}


id: GO:0003085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that reduces the force with which blood travels through the systemic arterial circulatory system.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of blood pressure","termid":"GO:0045776"},{"relation_name":"part_of","term_name":"regulation of systemic arterial blood pressure","termid":"GO:0003073"}],"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 systemic arterial blood pressure","termid":"GO:0003085"}


id: PBO:0044847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 131B","termid":"PBO:0044847"}


id: PBO:0054493
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 1893","termid":"PBO:0054493"}


id: MOD:00091
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-arginine residue to L-arginine amide.","definition_xrefs":["PubMed:2229025","PubMed:2753890","PubMed:743209","RESID:AA0082","ChEBI:145897"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-arginine residue","termid":"MOD:00902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-arginine amide","synonyms":[{"name":"(2S)-2-amino-5-[(diaminomethylidene)amino]pentanamide","type":"exact"},{"name":"2-amino-5-carbamimidamidopentanamide","type":"exact"},{"name":"2-amino-5-guanidinopentanamide","type":"exact"},{"name":"ArgN","type":"exact"},{"name":"L-arginine amide","type":"exact"},{"name":"MOD_RES Arginine amide","type":"exact"},{"name":"amidated L-arginine","type":"exact"},{"name":"argininamide","type":"exact"}],"termid":"MOD:00091"}


id: PBO:0070722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 27","termid":"PBO:0070722"}


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


id: PBO:0119643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RFTN1 antisense RNA 1","termid":"PBO:0119643"}


id: PBO:0059186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MRFAP1 pseudogene 1","termid":"PBO:0059186"}


id: GO:0042483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the formation and development of a tooth or teeth.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of odontogenesis","termid":"GO:0042481"},{"relation_name":"is_a","term_name":"negative regulation of animal organ morphogenesis","termid":"GO:0110111"},{"relation_name":"negatively_regulates","term_name":"odontogenesis","termid":"GO:0042476"}],"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 odontogenesis","secondary_identifiers":["GO:0042486"],"synonyms":[{"name":"down regulation of odontogenesis","type":"exact"},{"name":"down-regulation of odontogenesis","type":"exact"},{"name":"downregulation of odontogenesis","type":"exact"},{"name":"inhibition of odontogenesis","type":"narrow"},{"name":"negative regulation of odontogenesis of calcareous or chitinous tooth","type":"narrow"},{"name":"negative regulation of tooth development","type":"exact"}],"termid":"GO:0042483"}


id: FYPO:0004932
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which one or more proteins is localized to the prospore membrane for a longer time than normal.","definition_xrefs":["PMID:20410137","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to prospore membrane","termid":"FYPO:0000677"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"increased duration of protein localization to prospore membrane","synonyms":[{"name":"increased duration of protein localisation to prospore membrane","type":"exact"},{"name":"increased duration of protein localization to forespore membrane","type":"exact"},{"name":"prolonged protein localization to prospore membrane","type":"exact"}],"termid":"FYPO:0004932"}


id: GO:0019290
data:
  {"annotated_genes":["SJAG_04031","SJAG_04032","SJAG_00469","SJAG_00792"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107199,95885,59554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031169"},{"annotations":[95831],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905569"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of siderophores, low molecular weight Fe(III)-chelating substances made by aerobic or facultatively anaerobic bacteria, especially when growing under iron deficient conditions. The complexes of Fe(3+)-siderophores have very high stability constants and are taken up by specific transport systems by microorganisms; the subsequent release of iron requires enzymatic action.","definition_xrefs":["PMID:20376388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore metabolic process","termid":"GO:0009237"},{"relation_name":"is_a","term_name":"nonribosomal peptide biosynthetic process","termid":"GO:0019184"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00469":null,"SJAG_00792":null,"SJAG_04031":null,"SJAG_04032":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"siderophore biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0031180","GO:0031178"],"synonyms":[{"name":"siderochrome biosynthesis","type":"narrow"},{"name":"siderochrome biosynthetic process","type":"narrow"},{"name":"siderophore anabolism","type":"exact"},{"name":"siderophore biosynthesis","type":"exact"},{"name":"siderophore biosynthetic process, peptide formation","type":"narrow"},{"name":"siderophore biosynthetic process, peptide modification","type":"narrow"},{"name":"siderophore formation","type":"exact"},{"name":"siderophore synthesis","type":"exact"}],"termid":"GO:0019290","terms_by_termid":{"GO:0031169":null,"GO:1905569":null}}


id: GO:1901126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of candicidin.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00101","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"candicidin metabolic process","termid":"GO:1901125"}],"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":"candicidin catabolic process","synonyms":[{"name":"candicidin breakdown","type":"exact"},{"name":"candicidin catabolism","type":"exact"},{"name":"candicidin degradation","type":"exact"}],"termid":"GO:1901126"}


id: PBO:0066502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger and WD repeat domain 3","termid":"PBO:0066502"}


id: PBO:0039331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arachidonate lipoxygenase 3 pseudogene 1","termid":"PBO:0039331"}


id: GO:0060263
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate frequency or extent of a phase of elevated metabolic activity, during which oxygen consumption increases; this leads to the production, by an NADH dependent system, of hydrogen peroxide (H2O2), superoxide anions and hydroxyl radicals.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"respiratory burst","termid":"GO:0045730"}],"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 respiratory burst","termid":"GO:0060263"}


id: PBO:0054091
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 1444","termid":"PBO:0054091"}


id: GO:0035201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation and/or maintenance of a lineage boundary between anterior and posterior compartments of the leg disc that cells cannot cross, thus separating the populations of cells in each compartment.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior/posterior lineage restriction, imaginal disc","termid":"GO:0048099"},{"relation_name":"part_of","term_name":"leg disc anterior/posterior pattern formation","termid":"GO:0035200"}],"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":"leg disc anterior/posterior lineage restriction","termid":"GO:0035201"}


id: GO:0019982
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to interleukin-7.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"},{"relation_name":"is_a","term_name":"cytokine binding","termid":"GO:0019955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"interleukin-7 binding","synonyms":[{"name":"IL-7 binding","type":"exact"}],"termid":"GO:0019982"}


id: PBO:0060109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 10","termid":"PBO:0060109"}


id: PBO:0053520
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 513","termid":"PBO:0053520"}


id: PBO:0073228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO specific peptidase 1","termid":"PBO:0073228"}


id: PBO:0080666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WAP four-disulfide core domain 11","termid":"PBO:0080666"}


id: GO:0106011
data:
  {"annotated_genes":["SJAG_03602","SJAG_04597"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140325"},{"annotations":[100212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120047"}]},"cv_name":"biological_process","definition":"Any process that regulates the localization of a protein to the medial cortex.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell division site","termid":"GO:1901900"},{"relation_name":"is_a","term_name":"regulation of protein localization to cell cortex","termid":"GO:1904776"},{"relation_name":"regulates","term_name":"protein localization to medial cortex","termid":"GO:0071574"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03602":null,"SJAG_04597":null},"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 localization to medial cortex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0106011","terms_by_termid":{"GO:0120047":null,"GO:0140325":null}}


id: GO:0099014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a neuronal dense core vesicle.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dense core granule organization","termid":"GO:0061109"}],"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":"neuronal dense core vesicle organization","termid":"GO:0099014"}


id: PBO:0046613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group MER34 member 1, envelope","termid":"PBO:0046613"}


id: PBO:0002678
data:
  {"annotated_genes":["SJAG_MIT03"],"annotation_feature_type":"gene","cv_annotations":{"EC numbers":[{"annotations":[56283],"is_not":false,"summary":null,"term":"PBO:0002678"}]},"cv_name":"EC numbers","gene_count":1,"genes_by_uniquename":{"SJAG_MIT03":null},"genotype_count":0,"is_obsolete":false,"name":"1.10.2.2","termid":"PBO:0002678","terms_by_termid":{"PBO:0002678":null}}


id: PBO:0040370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase peripheral stalk-membrane subunit b pseudogene 7","termid":"PBO:0040370"}


id: PBO:0012266
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferric reductase in pombe","termid":"PBO:0012266"}


id: PBO:0063690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphogluconate dehydrogenase pseudogene 2","termid":"PBO:0063690"}


id: PBO:0046739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exonuclease 5","termid":"PBO:0046739"}


id: GO:0050517
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reactions: ATP + 1D-myo-inositol hexakisphosphate = ADP + 5-diphospho-1D-myo-inositol (1,2,3,4,6)pentakisphosphate, and ATP + 1D-myo-inositol 1,3,4,5,6-pentakisphosphate = ADP + diphospho-1D-myo-inositol tetrakisphosphate (isomeric configuration unknown).","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete inositol hexakisphosphate kinase activity (obsolete GO:0050517)","synonyms":[{"name":"inositol hexakisphosphate kinase activity","type":"exact"},{"name":"inositol-hexakisphosphate kinase activity","type":"exact"}],"termid":"GO:0050517"}


id: GO:0048806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the genitalia over time, from its formation to the mature structure.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ development","termid":"GO:0048513"},{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"},{"relation_name":"part_of","term_name":"sex differentiation","termid":"GO:0007548"}],"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":"genitalia development","synonyms":[{"name":"genital development","type":"exact"}],"termid":"GO:0048806"}


id: GO:0032220
data:
  {"annotated_genes":["SJAG_04887","SJAG_00870","SJAG_02878","SJAG_02351","SJAG_02924"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79477,94126,97075,98155,112018],"is_not":false,"summary":null,"term":"GO:0032220"}]},"cv_name":"biological_process","definition":"The joining of two or more lipid bilayer membranes that surround cells, that contributes to cytogamy.","definition_xrefs":["GOC:mah","PMID:29134248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane fusion","termid":"GO:0045026"},{"relation_name":"part_of","term_name":"cytogamy","termid":"GO:0000755"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00870":null,"SJAG_02351":null,"SJAG_02878":null,"SJAG_02924":null,"SJAG_04887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0061024","GO:0000747","GO:0008150"],"is_obsolete":false,"name":"plasma membrane fusion involved in cytogamy","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0070872"],"synonyms":[{"name":"plasma membrane fusion during cytogamy","type":"related"},{"name":"plasma membrane organization involved in conjugation with cellular fusion","type":"exact"}],"termid":"GO:0032220","terms_by_termid":{"GO:0032220":null}}


id: GO:1901998
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a toxin into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:dph","GOC:TermGenie","PMID:17118486"],"gene_count":0,"genotype_count":0,"name":"obsolete toxin transport (obsolete GO:1901998)","termid":"GO:1901998"}


id: GO:0003361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an noradrenergic neuron that is part of the brainstem.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"noradrenergic neuron differentiation","termid":"GO:0003357"},{"relation_name":"part_of","term_name":"brainstem development","termid":"GO:0003360"}],"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":"noradrenergic neuron differentiation involved in brainstem development","termid":"GO:0003361"}


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:0090830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane TRP-like calcium ion channel Pkd2","termid":"PBO:0090830"}


id: MONDO:0000821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0000821 (obsolete MONDO:0000821)","termid":"MONDO:0000821","xrefs":{"Monarch":{"xref_id":"0000821"}}}


id: GO:1900468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of phosphatidylserine biosynthetic process.","definition_xrefs":["GOC:dgf","GOC:TermGenie","PMID:8614637","PMID:8056324"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phospholipid biosynthetic process","termid":"GO:0071071"},{"relation_name":"is_a","term_name":"regulation of phosphatidylserine metabolic process","termid":"GO:0150178"},{"relation_name":"regulates","term_name":"phosphatidylserine biosynthetic process","termid":"GO:0006659"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of phosphatidylserine biosynthetic process","synonyms":[{"name":"regulation of phosphatidylserine anabolism","type":"exact"},{"name":"regulation of phosphatidylserine biosynthesis","type":"exact"},{"name":"regulation of phosphatidylserine formation","type":"exact"},{"name":"regulation of phosphatidylserine synthesis","type":"exact"}],"termid":"GO:1900468"}


id: GO:0080021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a benzoic acid stimulus.","definition_xrefs":["PMID:18753285"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to benzoic acid","synonyms":[{"name":"response to benzoic acid stimulus","type":"exact"}],"termid":"GO:0080021"}


id: MONDO:0005515
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the oral cavity. The majority are squamous cell carcinomas.","definition_xrefs":["NCIT:C9314"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"},{"relation_name":"is_a","term_name":"oral cavity neoplasm","termid":"MONDO:0021245"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"oral cavity cancer","secondary_identifiers":["ICD9:144.9","ICD9:145.9","DOID:8618","ICD9:144.0","ICD9:145.8","EFO:0005570","ICD9:149.8","ICD9:144","MEDGEN:56298","UMLS:C0153381","ICD9:144.1","SCTID:363385007","SCTID:363505006"],"synonyms":[{"name":"cancer of oral cavity","type":"exact"},{"name":"malignant mouth neoplasm","type":"exact"},{"name":"malignant mouth tumor","type":"exact"},{"name":"malignant mouth tumour","type":"exact"},{"name":"malignant neoplasm of anterior portion of floor of mouth","type":"narrow"},{"name":"malignant neoplasm of floor of mouth","type":"narrow"},{"name":"malignant neoplasm of lateral floor of mouth","type":"narrow"},{"name":"malignant neoplasm of lateral portion of floor of mouth","type":"narrow"},{"name":"malignant neoplasm of mouth","type":"exact"},{"name":"malignant neoplasm of oral cavity","type":"exact"},{"name":"malignant neoplasm of the mouth","type":"exact"},{"name":"malignant oral cavity neoplasm","type":"exact"},{"name":"malignant oral cavity tumor","type":"exact"},{"name":"malignant oral cavity tumour","type":"exact"},{"name":"malignant tumor of anterior floor of mouth","type":"exact"},{"name":"malignant tumor of lateral floor of mouth","type":"exact"},{"name":"malignant tumor of mouth","type":"exact"},{"name":"malignant tumor of oral cavity","type":"exact"},{"name":"malignant tumor of the floor of the mouth","type":"narrow"},{"name":"malignant tumor of the mouth","type":"exact"},{"name":"malignant tumour of anterior floor of mouth","type":"exact"},{"name":"malignant tumour of lateral floor of mouth","type":"exact"},{"name":"malignant tumour of mouth","type":"exact"},{"name":"malignant tumour of oral cavity","type":"exact"},{"name":"malignant tumour of the floor of the mouth","type":"narrow"},{"name":"malignant tumour of the mouth","type":"exact"},{"name":"mouth cancer","type":"related"},{"name":"oral cavity cancer","type":"exact"}],"termid":"MONDO:0005515","xrefs":{"Monarch":{"xref_id":"0005515"}}}


id: PBO:0055895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 15","termid":"PBO:0055895"}


id: PBO:0087994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tryptophan 2,3-dioxygenase or indoleamine 2,3-dioxygenase; required for de novo biosynthesis of NAD+ from tryptophan via kynurenine; up-regulated by telomere uncapping, and interacts genetically with capping gene CDC13; overexpression reduces lipid droplet accumulation by skewing glycolytic flux towards biosynthesis of shikimate, aromatic amino acids, and NAD+ during aging and extends lifespan; regulated by Hst1p and Aftp","termid":"PBO:0087994"}


id: MONDO:0002278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm arising from the wall of the colon.","definition_xrefs":["NCIT:C2894"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colonic neoplasm","termid":"MONDO:0005401"},{"relation_name":"is_a","term_name":"benign neoplasm of large intestine","termid":"MONDO:0021444"}],"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":"benign colon neoplasm","secondary_identifiers":["MONDO:0021466","DOID:235","SCTID:92065004","ICD9:211.3","MEDGEN:525","UMLS:C0004991"],"synonyms":[{"name":"benign colon neoplasm","type":"exact"},{"name":"benign colon tumor","type":"exact"},{"name":"benign colon tumour","type":"exact"},{"name":"benign colonic neoplasm","type":"exact"},{"name":"benign colonic tumor","type":"exact"},{"name":"benign colonic tumour","type":"exact"},{"name":"benign neoplasm of colon","type":"exact"},{"name":"benign neoplasm of the colon","type":"exact"},{"name":"benign tumor of colon","type":"exact"},{"name":"benign tumor of the colon","type":"exact"},{"name":"benign tumour of colon","type":"exact"},{"name":"benign tumour of the colon","type":"exact"},{"name":"colon benign neoplasm","type":"exact"},{"name":"colon neoplasm","type":"broad"},{"name":"colonic Mass","type":"exact"},{"name":"colonic benign neoplasm","type":"related"},{"name":"colonic tumor","type":"broad"},{"name":"colonic tumour","type":"broad"}],"termid":"MONDO:0002278","xrefs":{"Monarch":{"xref_id":"0002278"}}}


id: PBO:0068839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 77, pseudogene","termid":"PBO:0068839"}


id: FYPO:0005304
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through interphase of the mitotic cell cycle is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of mitotic cell cycle phase","termid":"FYPO:0001069"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000631","FYPO:0001320"],"is_obsolete":false,"name":"increased duration of mitotic interphase","synonyms":[{"name":"decreased rate of mitotic interphase progression","type":"related"},{"name":"delayed mitotic interphase progression","type":"related"},{"name":"delayed mitotic interphase progression during vegetative growth","type":"related"},{"name":"increased duration of interphase during mitotic cell cycle","type":"exact"},{"name":"increased duration of mitotic interphase during vegetative growth","type":"exact"},{"name":"prolonged mitotic interphase","type":"exact"},{"name":"reduced rate of mitotic interphase progression","type":"related"}],"termid":"FYPO:0005304"}


id: MONDO:0029810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete laminopathy with striated muscle involvement (obsolete MONDO:0029810)","secondary_identifiers":["Orphanet:300755"],"termid":"MONDO:0029810","xrefs":{"Monarch":{"xref_id":"0029810"}}}


id: MONDO:0012062
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ABCC9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"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":"dilated cardiomyopathy 1O","secondary_identifiers":["UMLS:C1837839","GARD:15434","MEDGEN:325268","OMIM:608569","DOID:0110451","MESH:C563906"],"synonyms":[{"name":"ABCC9 familial isolated dilated cardiomyopathy","type":"exact"},{"name":"CMD1O","type":"exact"},{"name":"cardiomyopathy, dilated, 1O","type":"related"},{"name":"cardiomyopathy, dilated, type 1O","type":"exact"},{"name":"cardiomyopathy, dilated, with ventricular tachycardia","type":"related"},{"name":"dilated cardiomyopathy type 1O","type":"exact"},{"name":"dilated cardiomyopathy with ventricular tachycardia","type":"exact"},{"name":"familial isolated dilated cardiomyopathy caused by mutation in ABCC9","type":"exact"}],"termid":"MONDO:0012062","xrefs":{"Monarch":{"xref_id":"0012062"}}}


id: PR:Q09691
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrf1 gene.","definition_xrefs":["UniProtKB:Q09691","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":"peptide chain release factor 1, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2F7.17","synonyms":[{"name":"MRF-1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"MtRF-1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-mrf1","type":"exact"}],"termid":"PR:Q09691"}


id: PBO:0055090
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 2508","termid":"PBO:0055090"}


id: PR:Q09887
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cationic amino acid transporter 4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04711","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized amino-acid permease C584.13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC584.13","secondary_identifiers":["UniProtKB:Q09887"],"synonyms":[{"name":"Spom972h-SLC7A4","type":"exact"}],"termid":"PR:Q09887"}


id: PBO:0080841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y-box binding protein 1 pseudogene 5","termid":"PBO:0080841"}


id: PR:Q9USJ3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC4B3.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USJ3"],"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 C4B3.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4B3.03c","synonyms":[{"name":"Spom972h-SPCC4B3.03c","type":"exact"}],"termid":"PR:Q9USJ3"}


id: PBO:0018183
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae HMG2 catalytic domain","termid":"PBO:0018183"}


id: PBO:0064122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polycystin 2 like 2, transient receptor potential cation channel","termid":"PBO:0064122"}


id: GO:0034232
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of ascospore wall chitin, a linear polysaccharide consisting of P-1,4-linked N-acetyl-D-glucosamine residues, found in the walls of ascospores.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete ascospore wall chitin catabolic process (obsolete GO:0034232)","synonyms":[{"name":"ascospore wall chitin breakdown","type":"exact"},{"name":"ascospore wall chitin catabolism","type":"exact"},{"name":"ascospore wall chitin degradation","type":"exact"}],"termid":"GO:0034232"}


id: PBO:0064103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi like RNA-mediated gene silencing 4","termid":"PBO:0064103"}


id: GO:0033476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an indole-3-acetic acid amide conjugate, a form of indoleacetic acid covalently bound to an a sugar or polyol through an ester bond.","definition_xrefs":["GOC:mah","MetaCyc:PWY-1741"],"direct_ancestors":[{"relation_name":"is_a","term_name":"indoleacetic acid conjugate biosynthetic process","termid":"GO:0033474"}],"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":"indoleacetic acid ester conjugate biosynthetic process","synonyms":[{"name":"IAA ester conjugate biosynthetic process","type":"exact"},{"name":"indole acetic acid ester conjugate biosynthesis","type":"exact"},{"name":"indole acetic acid ester conjugate biosynthetic process","type":"exact"},{"name":"indoleacetic acid ester conjugate anabolism","type":"exact"},{"name":"indoleacetic acid ester conjugate biosynthesis","type":"exact"},{"name":"indoleacetic acid ester conjugate formation","type":"exact"},{"name":"indoleacetic acid ester conjugate synthesis","type":"exact"}],"termid":"GO:0033476"}


id: FYPO:0001705
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which any mitotic DNA damage checkpoint is normal (i.e. indistinguishable from wild type). A DNA damage checkpoint normally regulates progression through the cell cycle in response to DNA damage.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular response to stress during vegetative growth","termid":"FYPO:0000968"},{"relation_name":"is_a","term_name":"normal mitotic cell cycle checkpoint","termid":"FYPO:0001703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000631"],"is_obsolete":false,"name":"normal mitotic DNA damage checkpoint","synonyms":[{"name":"normal DNA damage checkpoint during mitotic cell cycle","type":"exact"},{"name":"normal mitotic DNA damage checkpoint activation","type":"exact"},{"name":"normal mitotic DNA damage checkpoint activation under non-stressed conditions","type":"narrow"},{"name":"normal mitotic DNA damage checkpoint during cellular response to DNA damage","type":"exact"},{"name":"normal mitotic DNA damage checkpoint during vegetative growth","type":"exact"}],"termid":"FYPO:0001705"}


id: MONDO:0034895
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare syndromic esophageal malformation characterized by severe congenital brachyesophagus with midline diaphragmatic hernia and secondary intrathoracic stomach, and vertebral anomalies (in particular rachischisis of the cervical/thoracic spine). Additional reported manifestations include intrauterine growth restriction, short neck, intestinal malrotation, herniation of other abdominal organs, and cleft lip, among others. The condition is mostly fatal in the neonatal or early infantile period.","definition_xrefs":["Orphanet:514352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome","secondary_identifiers":["UMLS:C5680208","MEDGEN:1807957","GARD:22076"],"synonyms":[{"name":"serpentine-like syndrome","type":"exact"}],"termid":"MONDO:0034895","xrefs":{"Monarch":{"xref_id":"0034895"}}}


id: PBO:0000964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inorganic diphosphatase (predicted)","termid":"PBO:0000964"}


id: GO:0003046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The intrinsic circulatory process resulting from stress relaxation that modulates the force with which blood travels through the systemic arterial circulatory system. Stress relaxation is the adaptation of vessels to a new size as a result of changes in pressure in storage areas such as veins, the liver, the spleen, and the lungs.","definition_xrefs":["GOC:mtg_cardio","ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure by physical factors","termid":"GO:0003045"},{"relation_name":"is_a","term_name":"negative regulation of systemic arterial blood pressure","termid":"GO:0003085"}],"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 stress relaxation","synonyms":[{"name":"blood pressure regulation by stress relaxation","type":"exact"}],"termid":"GO:0003046"}


id: PBO:0058887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 10524","termid":"PBO:0058887"}


id: GO:2001031
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of cellular glucuronidation.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cellular glucuronidation (obsolete GO:2001031)","synonyms":[{"name":"positive regulation of cellular glucuronide biosynthesis","type":"exact"},{"name":"positive regulation of cellular glucuronide biosynthetic process","type":"exact"},{"name":"positive regulation of cellular glucuronoside biosynthesis","type":"exact"},{"name":"positive regulation of cellular glucuronoside biosynthetic process","type":"exact"}],"termid":"GO:2001031"}


id: PBO:0030611
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_alpha-glucan_level","termid":"PBO:0030611"}


id: GO:0033602
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 dopamine.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of dopamine secretion","termid":"GO:0014059"},{"relation_name":"is_a","term_name":"negative regulation of catecholamine secretion","termid":"GO:0033604"},{"relation_name":"negatively_regulates","term_name":"dopamine secretion","termid":"GO:0014046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of dopamine secretion","synonyms":[{"name":"down regulation of dopamine secretion","type":"exact"},{"name":"down-regulation of dopamine secretion","type":"exact"},{"name":"downregulation of dopamine secretion","type":"exact"},{"name":"inhibition of dopamine secretion","type":"narrow"}],"termid":"GO:0033602"}


id: MONDO:0956996
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An IDH-mutant, and 1p/19q-codeleted oligodendroglioma that is characterized as a well differentiated tumor lacking anaplastic features (brisk mitotic activity, microvascular proliferation, necrosis).","definition_xrefs":["DOID:0081281"],"direct_ancestors":[{"relation_name":"is_a","term_name":"IDH-mutant and 1p/19q-codeleted oligodendroglioma","termid":"MONDO:0859592"}],"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":"oligodendroglioma, IDH-mutant and 1p/19q-codeleted grade 2","termid":"MONDO:0956996","xrefs":{"Monarch":{"xref_id":"0956996"}}}


id: MONDO:0009732
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital nephrotic syndrome, Finnish type is characterized by protein loss beginning during fetal life.","definition_xrefs":["Orphanet:839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial nephrotic syndrome","termid":"MONDO:0002350"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"congenital nephrotic syndrome, Finnish type","secondary_identifiers":["MEDGEN:98011","DOID:0080390","GARD:1500","MedDRA:10060740","SCTID:197601003","NANDO:2200110","NCIT:C122795","UMLS:C0403399","OMIM:256300"],"synonyms":[{"name":"CnF","type":"related"},{"name":"Finnish congenital nephrosis","type":"exact"},{"name":"NPHS1","type":"related"},{"name":"congenital nephrotic syndrome - Finnish type","type":"exact"},{"name":"congenital nephrotic syndrome 1","type":"related"},{"name":"congenital nephrotic syndrome Finnish type","type":"related"},{"name":"congenital nephrotic syndrome, Finnish type","type":"exact"},{"name":"nephrosis 1, congenital, Finnish type","type":"related"},{"name":"nephrosis, congenital","type":"related"},{"name":"nephrotic syndrome - NPHS1 associated","type":"exact"},{"name":"nephrotic syndrome, congenital","type":"related"},{"name":"nephrotic syndrome, type 1","type":"related"}],"termid":"MONDO:0009732","xrefs":{"Monarch":{"xref_id":"0009732"}}}


id: GO:0090307
data:
  {"annotated_genes":["SJAG_02246","SJAG_03116","SJAG_03540","SJAG_03073","SJAG_00794","SJAG_02609","SJAG_01613","SJAG_01224","SJAG_02336","SJAG_01546","SJAG_00773","SJAG_03062","SJAG_04745","SJAG_07018","SJAG_04841","SJAG_03835","SJAG_02761","SJAG_01215","SJAG_04464","SJAG_01297","SJAG_04901","SJAG_02332"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98652,102780,111433,112412,120532],"is_not":false,"summary":null,"term":"GO:0090307"},{"annotations":[79505,77501,97093],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000073"},{"annotations":[104848,75768,98551,101007],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990810"},{"annotations":[100407,103237,99063,102173,110079,105695,101643],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061804"},{"annotations":[101013,103238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140641"},{"annotations":[101014,110676,78859,96555,99064],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051256"},{"annotations":[113268],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0110161"},{"annotations":[73124],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1901673"}]},"cv_name":"biological_process","definition":"Mitotic bipolar spindle assembly begins with spindle microtubule nucleation from the separated spindle pole body, includes spindle elongation during prometaphase, and is complete when all kinetochores are stably attached the spindle, and the spindle assembly checkpoint is satisfied.","definition_xrefs":["GOC:tb","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic spindle organization","termid":"GO:0007052"},{"relation_name":"is_a","term_name":"spindle assembly","termid":"GO:0051225"},{"relation_name":"part_of","term_name":"mitotic sister chromatid segregation","termid":"GO:0000070"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00773":null,"SJAG_00794":null,"SJAG_01215":null,"SJAG_01224":null,"SJAG_01297":null,"SJAG_01546":null,"SJAG_01613":null,"SJAG_02246":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02609":null,"SJAG_02761":null,"SJAG_03062":null,"SJAG_03073":null,"SJAG_03116":null,"SJAG_03540":null,"SJAG_03835":null,"SJAG_04464":null,"SJAG_04745":null,"SJAG_04841":null,"SJAG_04901":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0000226"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0000070"}],"interesting_parent_ids":["GO:0007010","GO:0000226","GO:0000070","GO:0044085","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"mitotic spindle assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"spindle assembly involved in mitosis","type":"exact"}],"termid":"GO:0090307","terms_by_termid":{"GO:0000073":null,"GO:0051256":null,"GO:0061804":null,"GO:0090307":null,"GO:0110161":null,"GO:0140641":null,"GO:1901673":null,"GO:1990810":null}}


id: PBO:0087369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPOUT methyltransferase; catalyzes omega-monomethylation of Rps3p on Arg-146; not an essential gene; predicted to be involved in rRNA processing and ribosome biogenesis and in biopolymer catabolism","termid":"PBO:0087369"}


id: MONDO:0003437
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A small cell lung carcinoma detectable by sputum cytology only. The primary tumor is undetectable radiographically or during bronchoscopy; therefore, it can not be assessed.","definition_xrefs":["NCIT:C6683"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell lung carcinoma","termid":"MONDO:0008433"}],"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":"occult small cell lung carcinoma","secondary_identifiers":["DOID:5414","MEDGEN:233791","UMLS:C1335099"],"synonyms":[{"name":"lung occult small cell carcinoma","type":"related"},{"name":"occult small cell carcinoma of lung","type":"exact"},{"name":"occult small cell carcinoma of the lung","type":"exact"},{"name":"occult small cell lung carcinoma","type":"exact"}],"termid":"MONDO:0003437","xrefs":{"Monarch":{"xref_id":"0003437"}}}


id: PBO:0060960
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFKB inhibitor zeta","termid":"PBO:0060960"}


id: GO:1901054
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sarcosine.","definition_xrefs":["PMID:31402327","GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid biosynthetic process","termid":"GO:0042398"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid biosynthetic process","termid":"GO:0170043"},{"relation_name":"is_a","term_name":"sarcosine metabolic process","termid":"GO:1901052"},{"relation_name":"is_a","term_name":"alpha-amino acid biosynthetic process","termid":"GO:1901607"}],"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:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"sarcosine biosynthetic process","synonyms":[{"name":"sarcosine anabolism","type":"exact"},{"name":"sarcosine biosynthesis","type":"exact"},{"name":"sarcosine formation","type":"exact"},{"name":"sarcosine synthesis","type":"exact"}],"termid":"GO:1901054"}


id: PBO:0056343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase kinase kinase 2","termid":"PBO:0056343"}


id: FYPO:0003167
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of protein farnesyltransferase 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:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000652","FYPO:0000707","FYPO:0000661"],"is_obsolete":false,"name":"abnormal protein farnesyltransferase activity","termid":"FYPO:0003167"}


id: MONDO:0007935
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominantly inherited cystoid macular edema manifesting with macular atrophy, strabismus and, sometimes, pericentral retinitis pigmentosa. It is associated with a poor visual prognosis.","definition_xrefs":["Orphanet:75381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macular retinal edema","termid":"MONDO:0003005"}],"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":"cystoid macular edema","secondary_identifiers":["GARD:16694","ICD10CM:H35.5","UMLS:C0024440","DOID:4447","MEDGEN:7435","NCIT:C34794","OMIM:153880","SCTID:312921000"],"synonyms":[{"name":"DCMD","type":"exact"},{"name":"Mddc","type":"related"},{"name":"autosomal dominant cystoid macular edema","type":"exact"},{"name":"autosomal dominant cystoid macular oedema","type":"exact"},{"name":"cystoid macular dystrophy","type":"related"},{"name":"familial macular edema","type":"exact"},{"name":"familial macular oedema","type":"exact"},{"name":"macular dystrophy, dominant cystoid","type":"related"},{"name":"macular edema, cystoid","type":"related"}],"termid":"MONDO:0007935","xrefs":{"Monarch":{"xref_id":"0007935"}}}


id: MONDO:0035759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"factor V atlanta bleeding disorder","secondary_identifiers":["MEDGEN:1842929","GARD:22415","Orphanet:600194","UMLS:C5681543"],"termid":"MONDO:0035759","xrefs":{"Monarch":{"xref_id":"0035759"}}}


id: PBO:0085609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in cytochrome c oxidase (Complex IV) assembly; involved in delivery of copper to Complex IV; also required for efficient formation of respiratory supercomplexes comprised of Complexes III and IV; localizes to the mitochondrial intermembrane space; ortholog implicated in cardiac defects in zebrafish and human; transcription is induced in response to the DNA-damaging agent MMS; protein abundance increases in response to DNA replication stress","termid":"PBO:0085609"}


id: PATO:0002251
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A degree of pigmentation quality that is relative low.","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":"pigmented","termid":"PATO:0002248"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased pigmentation","synonyms":[{"name":"hypopigmented","type":"exact"}],"termid":"PATO:0002251"}


id: GO:0035567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A type of Wnt signaling pathway in which Wnt binding to its receptor on the surface of a target cell results in the by propagation of the molecular signals via effectors other than beta-catenin.","definition_xrefs":["PMID:37804416"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Wnt signaling pathway","termid":"GO:0016055"}],"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":"non-canonical Wnt signaling pathway","secondary_identifiers":["Reactome:R-HSA-3858494"],"synonyms":[{"name":"beta-catenin-independent Wnt receptor signaling pathway","type":"exact"},{"name":"non-canonical Wnt receptor signaling pathway","type":"exact"},{"name":"non-canonical Wnt receptor signalling pathway","type":"exact"},{"name":"non-canonical Wnt-activated signaling pathway","type":"exact"}],"termid":"GO:0035567"}


id: PBO:0070091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 5 pseudogene","termid":"PBO:0070091"}


id: GO:1905272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of proton-transporting ATP synthase activity, rotational mechanism.","definition_xrefs":["GO_REF:0000059","PMID:21106936","GOC:TermGenie","GOC:als"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of proton-transporting ATP synthase activity, rotational mechanism (obsolete GO:1905272)","synonyms":[{"name":"down regulation of H+-transporting ATP synthase activity","type":"exact"},{"name":"down regulation of hydrogen ion translocating F-type ATPase activity","type":"exact"},{"name":"down regulation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"down regulation of hydrogen ion transporting two-sector ATPase activity","type":"exact"},{"name":"down regulation of proton-transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"down-regulation of H+-transporting ATP synthase activity","type":"exact"},{"name":"down-regulation of hydrogen ion translocating F-type ATPase activity","type":"exact"},{"name":"down-regulation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"down-regulation of hydrogen ion transporting two-sector ATPase activity","type":"exact"},{"name":"down-regulation of proton-transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"downregulation of H+-transporting ATP synthase activity","type":"exact"},{"name":"downregulation of hydrogen ion translocating F-type ATPase activity","type":"exact"},{"name":"downregulation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"downregulation of hydrogen ion transporting two-sector ATPase activity","type":"exact"},{"name":"downregulation of proton-transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"inhibition of H+-transporting ATP synthase activity","type":"narrow"},{"name":"inhibition of hydrogen ion translocating F-type ATPase activity","type":"narrow"},{"name":"inhibition of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"narrow"},{"name":"inhibition of hydrogen ion transporting two-sector ATPase activity","type":"narrow"},{"name":"inhibition of proton-transporting ATP synthase activity, rotational mechanism","type":"narrow"},{"name":"negative regulation of H+-transporting ATP synthase activity","type":"exact"},{"name":"negative regulation of hydrogen ion translocating F-type ATPase activity","type":"exact"},{"name":"negative regulation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"negative regulation of hydrogen ion transporting two-sector ATPase activity","type":"exact"}],"termid":"GO:1905272"}


