# terms

id: MONDO:0012797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"otosclerosis","termid":"MONDO:0005349"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otosclerosis 8","secondary_identifiers":["MEDGEN:436965","MESH:C567421","OMIM:612096","UMLS:C2677515","DOID:0060926"],"synonyms":[{"name":"OTSC8","type":"exact"},{"name":"otosclerosis 8","type":"exact"}],"termid":"MONDO:0012797","xrefs":{"Monarch":{"xref_id":"0012797"}}}


id: GO:0005309
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: creatine(out) + Na+(out) = creatine(in) + Na+(in).","definition_xrefs":["TC:2.A.22.3.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"creatine transmembrane transporter activity","termid":"GO:0005308"},{"relation_name":"is_a","term_name":"organic acid:sodium symporter activity","termid":"GO:0005343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"creatine:sodium symporter activity","secondary_identifiers":["Reactome:R-HSA-200396"],"synonyms":[{"name":"sodium/chloride-dependent creatine transporter","type":"broad"}],"termid":"GO:0005309"}


id: PBO:0058429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4799","termid":"PBO:0058429"}


id: GO:0000244
data:
  {"annotated_genes":["SJAG_00278","SJAG_04497","SJAG_02915","SJAG_00643","SJAG_04529","SJAG_00414","SJAG_01547","SJAG_03214"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63153,72342,75947,77247,105254,106308,111996,114127],"is_not":false,"summary":null,"term":"GO:0000244"}]},"cv_name":"biological_process","definition":"The formation of a tri-snRNP complex containing U4 and U6 (or U4atac and U6atac) snRNAs and U5 snRNAs and associated proteins. This includes reannealing of U4 and U6 (or U4atac and U6atac) snRNAs released from previous rounds of splicing to reform the U4/U6 snRNP (or U4atac/U6atac snRNP) as well as the subsequent association of the U5 snRNP with the U4/U6 snRNP (or U4atac/U6atac snRNP) to form a tri-snRNP that is ready to reassemble into another spliceosome complex.","definition_xrefs":["PMID:9452384","ISBN:0879695897"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal snRNP assembly","termid":"GO:0000387"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00278":null,"SJAG_00414":null,"SJAG_00643":null,"SJAG_01547":null,"SJAG_02915":null,"SJAG_03214":null,"SJAG_04497":null,"SJAG_04529":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0044085","GO:0010467","GO:0016071","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"spliceosomal tri-snRNP complex assembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0000351","GO:0000355"],"synonyms":[{"name":"assembly of spliceosomal tri-snRNP","type":"exact"},{"name":"assembly of spliceosomal tri-snRNP U4/U6.U5","type":"narrow"},{"name":"assembly of spliceosomal tri-snRNP U4atac/U6atac.U5","type":"narrow"},{"name":"snRNP recycling","type":"broad"},{"name":"spliceosomal tri-snRNP U4/U6.U5 assembly","type":"narrow"},{"name":"spliceosomal tri-snRNP U4atac/U6atac.U5 assembly","type":"narrow"},{"name":"spliceosomal tri-snRNP assembly","type":"exact"}],"termid":"GO:0000244","terms_by_termid":{"GO:0000244":null}}


id: MONDO:0024455
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant Robinow syndrome in which the cause of the disease is a mutation in the WNT5A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant Robinow syndrome","termid":"MONDO:0008389"}],"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":"autosomal dominant Robinow syndrome 1","secondary_identifiers":["UMLS:C4551475","GARD:2013","DOID:0060766","MEDGEN:1641736","OMIM:180700"],"synonyms":[{"name":"DRS1","type":"exact"},{"name":"Robinow dwarfism","type":"related"},{"name":"Robinow syndrome, autosomal dominant 1","type":"exact"},{"name":"WNT5A autosomal dominant Robinow syndrome","type":"exact"},{"name":"acral dysostosis with Facial and genital abnormalities","type":"related"},{"name":"autosomal dominant Robinow syndrome caused by mutation in WNT5A","type":"exact"},{"name":"dysostosis acral with facial and genital abnormalities","type":"exact"},{"name":"fetal face syndrome","type":"related"},{"name":"foetal face syndrome","type":"related"}],"termid":"MONDO:0024455","xrefs":{"Monarch":{"xref_id":"0024455"}}}


id: FYPO:0003421
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 nitric oxide measured in a cell is lower than normal during a cellular response to cadmium.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular nitric oxide level during vegetative growth","termid":"FYPO:0003127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased cellular nitric oxide level during cellular response to cadmium ion","synonyms":[{"name":"decreased cellular NO level during cellular response to cadmium","type":"exact"},{"name":"decreased cellular nitric oxide level during cellular response to cadmium","type":"exact"},{"name":"decreased cellular nitric oxide level during cellular response to cadmium during mitotic cell cycle","type":"related"},{"name":"decreased cellular nitric oxide level during cellular response to cadmium during vegetative growth","type":"exact"},{"name":"decreased nitric oxide accumulation during cellular response to cadmium","type":"related"},{"name":"reduced cellular nitric oxide level during cellular response to cadmium","type":"exact"}],"termid":"FYPO:0003421"}


id: FYPO:0004685
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to radicicol. Cells stop growing (and may die) at a concentration of radicicol that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0000139","FYPO:0002683","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to radicicol","synonyms":[{"name":"hypersensitive to radicicol","type":"exact"},{"name":"sensitive to radicicol during mitotic cell cycle","type":"related"},{"name":"sensitive to radicicol during vegetative growth","type":"exact"}],"termid":"FYPO:0004685"}


id: MONDO:0020860
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection of the fauces by Corynebacterium diphtheriae.","definition_xrefs":["NCIT:C34545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diphtheria","termid":"MONDO:0005504"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"faucial diphtheria","secondary_identifiers":["UMLS:C0012556","MEDGEN:3857","ICD9:032.0","SCTID:3419005"],"synonyms":[{"name":"Diphtheritic membrane","type":"related"},{"name":"Diphtheritic membranous angina","type":"related"},{"name":"Faucial Diphtheria","type":"related"},{"name":"Faucial diphtheria","type":"related"},{"name":"diphtheritic membrane","type":"related"},{"name":"diphtheritic membranous angina","type":"related"},{"name":"faucial diphtheria","type":"exact"}],"termid":"MONDO:0020860","xrefs":{"Monarch":{"xref_id":"0020860"}}}


id: MONDO:0002206
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that affects the sweat glands.","definition_xrefs":["NCIT:C4810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sweat gland neoplasm","termid":"MONDO:0002381"},{"relation_name":"is_a","term_name":"skin cancer","termid":"MONDO:0002898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"sweat gland cancer","secondary_identifiers":["DOID:2095","UMLS:C1321904","MEDGEN:231171"],"synonyms":[{"name":"cancer of sweat gland","type":"exact"},{"name":"malignant neoplasm of sweat gland","type":"exact"},{"name":"malignant neoplasm of the sweat gland","type":"exact"},{"name":"malignant sweat gland neoplasm","type":"exact"},{"name":"malignant tumor of sweat gland","type":"exact"},{"name":"malignant tumor of the sweat gland","type":"exact"},{"name":"malignant tumour of sweat gland","type":"exact"},{"name":"malignant tumour of the sweat gland","type":"exact"},{"name":"sweat gland cancer","type":"exact"},{"name":"sweat gland neoplasms, malignant","type":"exact"}],"termid":"MONDO:0002206","xrefs":{"Monarch":{"xref_id":"0002206"}}}


id: MONDO:0005992
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete trichinosis (obsolete MONDO:0005992)","termid":"MONDO:0005992","xrefs":{"Monarch":{"xref_id":"0005992"}}}


id: PBO:0068281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease H1 pseudogene 2","termid":"PBO:0068281"}


id: PBO:0036011
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_threonine_phosphorylation_during_vegetative_growth","termid":"PBO:0036011"}


id: MONDO:0002466
data:
  {"annotated_genes":["SJAG_03677"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"}]},"cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the eye","direct_ancestors":[{"relation_name":"is_a","term_name":"head and neck carcinoma","termid":"MONDO:0002038"},{"relation_name":"is_a","term_name":"ocular cancer","termid":"MONDO:0002236"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03677":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"eye carcinoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0848866","DOID:295","MEDGEN:208855","NCIT:C6079"],"synonyms":[{"name":"carcinoma of eye","type":"exact"},{"name":"carcinoma of eyeball of camera-type eye","type":"exact"},{"name":"carcinoma of the eye","type":"exact"},{"name":"eye carcinoma","type":"exact"},{"name":"eyeball of camera-type eye carcinoma","type":"exact"},{"name":"ocular carcinoma","type":"exact"}],"termid":"MONDO:0002466","terms_by_termid":{"MONDO:0014937":null},"xrefs":{"Monarch":{"xref_id":"0002466"}}}


id: GO:0047116
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD+ + 1,6-dihydroxycyclohexa-2,4-diene-1-carboxylate = NADH + CO2 + catechol.","definition_xrefs":["EC:1.3.1.25","MetaCyc:1.3.1.25-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"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":"1,6-dihydroxycyclohexa-2,4-diene-1-carboxylate dehydrogenase activity","secondary_identifiers":["RHEA:11560"],"synonyms":[{"name":"(1R,6R)-1,6-dihydroxycyclohexa-2,4-diene-1-carboxylate:NAD+ oxidoreductase (decarboxylating)","type":"related"},{"name":"2-hydro-1,2-dihydroxybenzoate dehydrogenase activity","type":"related"},{"name":"3,5-cyclohexadiene-1,2-diol-1-carboxylate dehydrogenase activity","type":"related"},{"name":"3,5-cyclohexadiene-1,2-diol-1-carboxylic acid dehydrogenase activity","type":"related"},{"name":"DHB dehydrogenase activity","type":"related"},{"name":"DHBDH activity","type":"related"},{"name":"cis-1,2-dihydroxycyclohexa-3,5-diene-1-carboxylate:NAD(+) oxidoreductase activity","type":"related"},{"name":"cis-1,2-dihydroxycyclohexa-3,5-diene-1-carboxylate:NAD+ oxidoreductase activity","type":"related"},{"name":"dihydrodihydroxybenzoate dehydrogenase activity","type":"related"}],"termid":"GO:0047116"}


id: FYPO:0006243
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which mitotic chromosome condensation is abnormal over short (less than 90 kb) ranges within a chromosome arm.","definition_xrefs":["PMID:28825727","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete abnormal short range intra-arm mitotic chromosome condensation during interphase (obsolete FYPO:0006243)","synonyms":[{"name":"abnormal short range intra-arm chromosome condensation during interphase of mitotic cell cycle","type":"exact"},{"name":"abnormal short range intra-arm chromosome condensation during mitotic interphase","type":"exact"},{"name":"abnormal short range intra-arm mitotic chromosome condensation during interphase during vegetative growth","type":"exact"}],"termid":"FYPO:0006243"}


id: PR:Q10475
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A SAFB-like transcription modulator that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01863"],"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":"eukaryotic translation initiation factor 4 gamma (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17C9.03","secondary_identifiers":["UniProtKB:Q10475"],"synonyms":[{"name":"Spom972h-SLTM","type":"exact"},{"name":"eIF-4-gamma (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eIF-4G (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10475"}


id: PBO:0059115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mov10 RISC complex RNA helicase","termid":"PBO:0059115"}


id: GO:0010834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that contributes to the maintenance of proper telomeric length and structure by affecting and monitoring the activity of telomeric proteins and shortening the telomeric DNA.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete telomere maintenance via telomere shortening (obsolete GO:0010834)","synonyms":[{"name":"telomere maintenance via telomere shortening","type":"exact"}],"termid":"GO:0010834"}


id: PBO:0025530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial iron-sulfur cluster assembly protein Isa2","termid":"PBO:0025530"}


id: GO:0060976
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the blood vessels of the heart over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel development","termid":"GO:0001568"},{"relation_name":"part_of","term_name":"heart development","termid":"GO:0007507"}],"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":"coronary vasculature development","synonyms":[{"name":"cardiac blood vessel development","type":"exact"},{"name":"cardiac vasculature development","type":"exact"},{"name":"coronary blood vessel development","type":"exact"},{"name":"heart blood vessel development","type":"exact"},{"name":"heart vasculature development","type":"exact"}],"termid":"GO:0060976"}


id: GO:0042610
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a CD8, a receptor found on the surface of thymocytes and cytotoxic and suppressor T-lymphocytes.","definition_xrefs":["GOC:jl","MSH:D016827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"CD8 receptor binding","termid":"GO:0042610"}


id: GO:0043952
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which unfolded proteins are transported across the cytoplasmic membrane in Gram-positive and Gram-negative bacteria by the Sec complex, in a process involving proteolytic cleavage of an N-terminal signal peptide.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transmembrane transport","termid":"GO:0071806"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"protein transport by the Sec complex","synonyms":[{"name":"protein secretion by the Sec complex","type":"narrow"},{"name":"protein translocation by the Sec complex","type":"narrow"}],"termid":"GO:0043952"}


id: PBO:0027988
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_without_cell_division,_abnormal_septum_morphology,_enlarged_nucleus","termid":"PBO:0027988"}


id: PBO:0072215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S18 pseudogene 14","termid":"PBO:0072215"}


id: MONDO:0008001
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":"milia, multiple eruptive","secondary_identifiers":["MEDGEN:83356","MESH:C562823","OMIM:157400","UMLS:C0343079","SCTID:238749001"],"synonyms":[{"name":"MEM","type":"related"},{"name":"milia, multiple eruptive","type":"exact"}],"termid":"MONDO:0008001","xrefs":{"Monarch":{"xref_id":"0008001"}}}


id: PBO:0029906
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K4_dimethylation_at_centromere_outer_repeat","termid":"PBO:0029906"}


id: GO:2000540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein geranylgeranylation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein modification process","termid":"GO:0031400"},{"relation_name":"is_a","term_name":"regulation of protein geranylgeranylation","termid":"GO:2000539"},{"relation_name":"negatively_regulates","term_name":"protein geranylgeranylation","termid":"GO:0018344"}],"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 geranylgeranylation","synonyms":[{"name":"negative regulation of C-terminal protein geranylgeranylation","type":"related"},{"name":"negative regulation of protein amino acid geranylgeranylation","type":"exact"}],"termid":"GO:2000540"}


id: SO:0001502
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An experimental feature with high sequence identity to another sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"experimental_feature","termid":"SO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high_identity_region","synonyms":[{"name":"high identity region","type":"exact"}],"termid":"SO:0001502"}


id: PBO:0075231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 5 pseudogene 1","termid":"PBO:0075231"}


id: MONDO:0020137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete frontotemporal degeneration with dementia (obsolete MONDO:0020137)","secondary_identifiers":["Orphanet:98535"],"termid":"MONDO:0020137","xrefs":{"Monarch":{"xref_id":"0020137"}}}


id: GO:0120146
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to sulfatide, also known as 3-O-sulfogalactosylceramide, SM4, or sulfated galactocerebroside. Sulfatide is a class of sulfoglycolipid, which are glycolipids that contain a sulfate group.","definition_xrefs":["PMID:3549017","PMID:29497057","Wikipedia:Sulfatide","GOC:krc","PMID:23574804","PMID:21525289","PMID:22619219","PMID:22977233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolipid binding","termid":"GO:0051861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0008289","GO:0003674"],"is_obsolete":false,"name":"sulfatide binding","synonyms":[{"name":"3-O-sulfogalactosylceramide binding","type":"exact"},{"name":"SM4 binding","type":"exact"},{"name":"sulfated galactocerebroside binding","type":"exact"}],"termid":"GO:0120146"}


id: PBO:0047899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(7)(q22)","termid":"PBO:0047899"}


id: FYPO:0005953
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the duration of cell cycle arrest or delay due to regulation by the mitotic G2 DNA damage checkpoint is greater than in wild type during a cellular response to ionizing radiation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of mitotic DNA damage checkpoint during cellular response to ionizing radiation","termid":"FYPO:0003490"},{"relation_name":"is_a","term_name":"abnormal mitotic G2 DNA damage checkpoint","termid":"FYPO:0004373"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000298","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"name":"increased duration of mitotic G2 DNA damage checkpoint during cellular response to ionizing radiation","synonyms":[{"name":"delayed mitotic G2 DNA damage checkpoint deactivation during cellular response to ionizing radiation","type":"exact"},{"name":"increased duration of mitotic G2 DNA damage checkpoint during cellular response to IR","type":"exact"},{"name":"prolonged mitotic G2 DNA damage checkpoint during cellular response to ionizing radiation","type":"exact"}],"termid":"FYPO:0005953"}


id: PBO:0046529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endoplasmic reticulum protein 29","termid":"PBO:0046529"}


id: PBO:0082067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-methyl-adenine DNA glycosylase; initiates base excision repair (BER) by removing damaged bases to create abasic sites that are subsequently repaired; expansion of BER repair removes alkylated bases resulting from alkylating agent-induced DNA damage, compensating for the lack of DNA repair by oxidative dealkylation; protein abundance increases in response to DNA replication stress","termid":"PBO:0082067"}


id: FYPO:0003966
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of protein measured in a cell during a cellular response to salt stress is higher than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0006551","FYPO:0001320"],"is_obsolete":false,"name":"increased protein level during cellular response to salt stress","synonyms":[{"name":"increased protein accumulation during cellular response to salt stress","type":"related"},{"name":"increased protein level during cellular response to salt stress during mitotic cell cycle","type":"related"},{"name":"increased protein level during cellular response to salt stress during vegetative growth","type":"exact"}],"termid":"FYPO:0003966"}


id: PBO:0006191
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-not_exists_during","termid":"PBO:0006191"}


id: PBO:0031618
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transposition","termid":"PBO:0031618"}


id: GO:0060134
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a startle magnitude is reduced when the startling stimulus is preceded by a low-intensity prepulse.","definition_xrefs":["GOC:dph","PMID:10341260"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to external stimulus","termid":"GO:0032102"},{"relation_name":"part_of","term_name":"startle response","termid":"GO:0001964"}],"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":"prepulse inhibition","secondary_identifiers":["Wikipedia:Prepulse_inhibition"],"synonyms":[{"name":"PPI","type":"related"},{"name":"pre-pulse inhibition","type":"exact"}],"termid":"GO:0060134"}


id: PATO:0001097
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001097 relative force value (obsolete PATO:0001097)","termid":"PATO:0001097"}


id: MONDO:0009188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Epilepsy telangiectasia syndrome is characterized by intellectual deficit, epilepsy, palpebral conjunctival telangiectasias and diminished serum IgA, particular facies and a shortened fifth finger. It has been reported in six siblings from a Mexican family. It is probably transmitted as an autosomal recessive trait.","definition_xrefs":["Orphanet:1951"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"epilepsy syndrome","termid":"MONDO:0015650"},{"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":"epilepsy-telangiectasia syndrome","secondary_identifiers":["OMIM:226850","GARD:2168","MESH:C535497","UMLS:C1856929","MEDGEN:384017"],"synonyms":[{"name":"epilepsy telangiectasia","type":"related"},{"name":"epilepsy-telangiectasia","type":"related"},{"name":"intellectual disability, epilepsy, palpebral conjunctival telangiectasias and IgA deficiency","type":"related"},{"name":"mental retardation, epilepsy, palpebral conjunctival telangiectasias and IgA deficiency","type":"related"}],"termid":"MONDO:0009188","xrefs":{"Monarch":{"xref_id":"0009188"}}}


id: MONDO:0009772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculorenocerebellar syndrome","secondary_identifiers":["UMLS:C1850331","MEDGEN:340516","MESH:C537739","OMIM:257970","Orphanet:2715","GARD:4050"],"synonyms":[{"name":"ORC syndrome","type":"related"},{"name":"absence of the cerebellar granular layer, intellectual disability, tapetoretinal degeneration and progressive glomerulopathy","type":"related"},{"name":"absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy","type":"related"},{"name":"oculorenocerebellar syndrome","type":"exact"}],"termid":"MONDO:0009772","xrefs":{"Monarch":{"xref_id":"0009772"}}}


id: PBO:0079927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"URGCP-MRPS24 readthrough","termid":"PBO:0079927"}


id: GO:0043175
data:
  {"annotated_genes":["SJAG_04933","SJAG_04353","SJAG_02898","SJAG_01610","SJAG_00139","SJAG_00483","SJAG_02203","SJAG_03118","SJAG_01151","SJAG_00448","SJAG_01744"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67045],"is_not":false,"summary":null,"term":"GO:0043175"},{"annotations":[71238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001042"},{"annotations":[64940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099122"},{"annotations":[77854,72276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990269"},{"annotations":[70748,78446,78436,72088,76183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000993"},{"annotations":[73557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000994"}]},"cv_name":"molecular_function","definition":"Binding to an RNA polymerase core enzyme, containing a specific subunit composition defined as the core enzyme.","definition_xrefs":["GOC:jl","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase binding","termid":"GO:0070063"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00139":null,"SJAG_00448":null,"SJAG_00483":null,"SJAG_01151":null,"SJAG_01610":null,"SJAG_01744":null,"SJAG_02203":null,"SJAG_02898":null,"SJAG_03118":null,"SJAG_04353":null,"SJAG_04933":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"RNA polymerase core enzyme binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"termid":"GO:0043175","terms_by_termid":{"GO:0000993":null,"GO:0000994":null,"GO:0001042":null,"GO:0043175":null,"GO:0099122":null,"GO:1990269":null}}


id: MONDO:0013963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CABP2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 93","secondary_identifiers":["MEDGEN:854875","OMIM:614899","GARD:22645","DOID:0110537","UMLS:C3888355"],"synonyms":[{"name":"CABP2 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"DFNB93","type":"narrow"},{"name":"autosomal recessive deafness 93","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 93","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in CABP2","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 93","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 93","type":"exact"},{"name":"deafness, autosomal recessive 93","type":"narrow"},{"name":"deafness, autosomal recessive type 93","type":"narrow"}],"termid":"MONDO:0013963","xrefs":{"Monarch":{"xref_id":"0013963"}}}


id: PATO:0001670
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A susceptibility toward an external stimulus which is lower than normal/average.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"susceptible toward","termid":"PATO:0001152"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased susceptibility toward","synonyms":[{"name":"decreased susceptibility","type":"exact"},{"name":"low susceptibility toward","type":"exact"}],"termid":"PATO:0001670"}


id: MONDO:0010813
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":"pancreatic beta cell agenesis with neonatal diabetes mellitus","secondary_identifiers":["Orphanet:28455","MEDGEN:325072","MESH:C538111","UMLS:C1838655","OMIM:600089"],"synonyms":[{"name":"diabetes mellitus, insulin-dependent, neonatal","type":"exact"},{"name":"pancreatic beta cell agenesis with neonatal diabetes mellitus","type":"exact"}],"termid":"MONDO:0010813","xrefs":{"Monarch":{"xref_id":"0010813"}}}


id: GO:0043069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of programmed cell death, cell death resulting from activation of endogenous cellular processes.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of programmed cell death","termid":"GO:0043067"},{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"negatively_regulates","term_name":"programmed cell death","termid":"GO:0012501"}],"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 programmed cell death","secondary_identifiers":["GO:0043072"],"synonyms":[{"name":"down regulation of programmed cell death","type":"exact"},{"name":"down-regulation of programmed cell death","type":"exact"},{"name":"downregulation of programmed cell death","type":"exact"},{"name":"inhibition of programmed cell death","type":"narrow"},{"name":"negative regulation of non-apoptotic programmed cell death","type":"narrow"}],"termid":"GO:0043069"}


id: FYPO:0003727
data:
  {"alleles_by_uniquename":{"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119088],"is_not":false,"summary":null,"term":"FYPO:0003727"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the glycan moiety of a glycoprotein in the cell wall does not contain galactose residues. In wild-type cells, glycoprotein glycans contain mannose and galactose residues in a 1:1.2 ratio, and the galactose residues are connected by alpha-1,2 linkages.","definition_xrefs":["PMID:9125114","PMID:11378902","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell wall during vegetative growth","termid":"FYPO:0002628"},{"relation_name":"is_a","term_name":"galactose absent from glycoprotein glycan","termid":"FYPO:0003291"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04697":null},"genotype_count":1,"genotypes_by_uniquename":{"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002946"},{"rel_name":"output_of","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0002274"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0003290"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0002494","FYPO:0002274","FYPO:0001985","FYPO:0002946","FYPO:0003290","FYPO:0000002"],"is_obsolete":false,"name":"galactose absent from cell wall glycoprotein glycan","references_by_uniquename":{"PMID:36058798":null},"single_locus_annotated_genes":["SJAG_04697"],"single_locus_genotype_uniquenames":["gms1delta"],"synonyms":[{"name":"abolished galactosylation of cell surface proteins","type":"related"},{"name":"alpha 1,2-linked galactose residues absent from cell wall glycoprotein","type":"exact"},{"name":"galactose absent from cell wall glycoprotein oligosaccharide","type":"related"},{"name":"galactose absent from glycoprotein glycan in cell wall","type":"exact"}],"termid":"FYPO:0003727","terms_by_termid":{"FYPO:0003727":null,"FYPO_EXT:0000001":null}}


id: PBO:0071039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 41","termid":"PBO:0071039"}


id: PBO:0046480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERCC excision repair 5, endonuclease","termid":"PBO:0046480"}


id: PBO:0062419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 59 pseudogene","termid":"PBO:0062419"}


id: GO:0031692
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an alpha-1B adrenergic receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adrenergic receptor binding","termid":"GO:0031690"}],"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:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"alpha-1B adrenergic receptor binding","synonyms":[{"name":"alpha-1B adrenergic receptor ligand","type":"narrow"}],"termid":"GO:0031692"}


id: MONDO:1010351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Age-related macular degeneration that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal degeneration, non-human animal","termid":"MONDO:1010326"},{"relation_name":"is_a","term_name":"perceptual disorders, non-human animal","termid":"MONDO:1011343"},{"relation_name":"is_a","term_name":"hereditary neurological disease, non-human animal","termid":"MONDO:1012972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"age-related macular degeneration, non-human animal","secondary_identifiers":["OMIA:002142"],"termid":"MONDO:1010351","xrefs":{"Monarch":{"xref_id":"1010351"}}}


id: GO:0047030
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: trans-4-hydroxycyclohexanecarboxylate + NAD+ = 4-oxocyclohexanecarboxylate + H+ + NADH.","definition_xrefs":["RHEA:17429","EC:1.1.1.226"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"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":"4-hydroxycyclohexanecarboxylate dehydrogenase activity","secondary_identifiers":["MetaCyc:1.1.1.226-RXN","KEGG_REACTION:R04307"],"synonyms":[{"name":"trans-4-hydroxycyclohexanecarboxylate dehydrogenase activity","type":"related"},{"name":"trans-4-hydroxycyclohexanecarboxylate:NAD+ 4-oxidoreductase activity","type":"related"}],"termid":"GO:0047030"}


id: GO:0102906
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate(3-) = (-)-7-epi-alpha-selinene + diphosphoric acid.","definition_xrefs":["EC:4.2.3.86","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"7-epi-alpha-selinene synthase activity","secondary_identifiers":["MetaCyc:RXN-8609","RHEA:30383"],"termid":"GO:0102906"}


id: PBO:0109131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CRIPTO pseudogene 4","termid":"PBO:0109131"}


id: GO:0035048
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a pre-mRNA splicing factor from the cytoplasm into the nucleus, across the nuclear membrane.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete splicing factor protein import into nucleus (obsolete GO:0035048)","synonyms":[{"name":"splicing factor protein transport from cytoplasm to nucleus","type":"exact"},{"name":"splicing factor protein-nucleus import","type":"exact"}],"termid":"GO:0035048"}


id: MONDO:0034189
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cholangitis","termid":"MONDO:0004789"},{"relation_name":"is_a","term_name":"autoimmune hepatitis","termid":"MONDO:0016264"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome","secondary_identifiers":["UMLS:C5680117","Orphanet:562639","GARD:22250","MEDGEN:1812237"],"termid":"MONDO:0034189","xrefs":{"Monarch":{"xref_id":"0034189"}}}


id: PBO:0087056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L27A; homologous to mammalian ribosomal protein L27, no bacterial homolog; RPL27A has a paralog, RPL27B, that arose from the whole genome duplication","termid":"PBO:0087056"}


id: GO:0046001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of progression through the preblastoderm mitotic cell cycle.","definition_xrefs":["GOC:dph","GOC:go_curators","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of preblastoderm mitotic cell cycle","termid":"GO:0007347"},{"relation_name":"is_a","term_name":"negative regulation of mitotic cell cycle, embryonic","termid":"GO:0045976"},{"relation_name":"negatively_regulates","term_name":"preblastoderm mitotic cell cycle","termid":"GO:0035185"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of preblastoderm mitotic cell cycle","synonyms":[{"name":"down regulation of progression through preblastoderm mitotic cell cycle","type":"exact"},{"name":"down-regulation of progression through preblastoderm mitotic cell cycle","type":"exact"},{"name":"downregulation of progression through preblastoderm mitotic cell cycle","type":"exact"},{"name":"inhibition of progression through preblastoderm mitotic cell cycle","type":"narrow"},{"name":"negative regulation of preblastoderm mitotic cell cycle progression","type":"exact"},{"name":"negative regulation of progression through preblastoderm mitotic cell cycle","type":"exact"}],"termid":"GO:0046001"}


id: PBO:0061325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore complex interacting protein family member B3","termid":"PBO:0061325"}


id: PBO:0078356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 2-2","termid":"PBO:0078356"}


id: PBO:0075761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/arginine repetitive matrix 1 pseudogene 3","termid":"PBO:0075761"}


id: GO:0003036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which information about the levels of hydrogen ions are received and are converted to a molecular signal by chemoreceptors in an aortic body.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of pH by chemoreceptor signaling","termid":"GO:0003022"},{"relation_name":"part_of","term_name":"detection of hypoxic conditions in blood by aortic body chemoreceptor signaling","termid":"GO:0003033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of pH by aortic body chemoreceptor signaling","synonyms":[{"name":"detection of pH by aortic body chemoreceptor signalling","type":"exact"}],"termid":"GO:0003036"}


id: PBO:0062719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily Q member 1","termid":"PBO:0062719"}


id: GO:0106362
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-arginyl-[protein] + UDP-N-acetyl-alpha-D-glucosamine = H+ + N(omega)-(N-acetyl-beta-D-glucosaminyl)-L-arginyl-[protein] + UDP.","definition_xrefs":["GOC:sp","PMID:23955153","RHEA:66632","PMID:30619781"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein N-acetylglucosaminyltransferase activity","termid":"GO:0016262"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016757","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"protein-arginine N-acetylglucosaminyltransferase activity","termid":"GO:0106362"}


id: GO:0032329
data:
  {"annotated_genes":["SJAG_04588","SJAG_03256"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103590],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090516"},{"annotations":[65244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015825"},{"annotations":[90381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140300"}]},"cv_name":"biological_process","definition":"The directed movement of L-serine, 2-amino-3-hydroxypropanoic acid, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"neutral amino acid transport","termid":"GO:0015804"},{"relation_name":"is_a","term_name":"carboxylic acid transport","termid":"GO:0046942"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03256":null,"SJAG_04588":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"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"serine transport","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:0090478"],"synonyms":[{"name":"serine import","type":"narrow"}],"termid":"GO:0032329","terms_by_termid":{"GO:0015825":null,"GO:0090516":null,"GO:0140300":null}}


id: GO:0036363
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The release of transforming growth factor beta (TGF-beta) from its latent state. TGF-beta is secreted as part of a large latent complex (LLC) that is targeted to the extracellular matrix. Release of TGFbeta from its latent state is required for TGFbeta to bind to its receptors, and can occur by a variety of mechanisms.","definition_xrefs":["PMID:12482908","GOC:sl","GOC:bf","PMID:9170210"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta activation (obsolete GO:0036363)","synonyms":[{"name":"L-TGF-beta activation","type":"exact"},{"name":"TGF-B activation","type":"exact"},{"name":"TGF-beta activation","type":"exact"},{"name":"TGFB activation","type":"exact"},{"name":"TGFbeta activation","type":"exact"},{"name":"latent TGF-beta activation","type":"exact"}],"termid":"GO:0036363"}


id: MONDO:0013530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial atrial fibrillation in which the cause of the disease is a mutation in the SCN5A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial atrial fibrillation","termid":"MONDO:0018054"}],"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":"atrial fibrillation, familial, 10","secondary_identifiers":["GARD:15745","MEDGEN:462814","OMIM:614022","UMLS:C3151464"],"synonyms":[{"name":"ATFB10","type":"related"},{"name":"SCN5A familial atrial fibrillation","type":"exact"},{"name":"atrial fibrillation, familial, 10","type":"exact"},{"name":"atrial fibrillation, familial, type 10","type":"exact"},{"name":"familial atrial fibrillation caused by mutation in SCN5A","type":"exact"}],"termid":"MONDO:0013530","xrefs":{"Monarch":{"xref_id":"0013530"}}}


id: PR:Q9HE02
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- med13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HE02"],"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":"mediator of RNA polymerase II transcription subunit 13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC589.02c","synonyms":[{"name":"Spom972h-med13","type":"exact"},{"name":"mediator complex subunit 13 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"suppressor of RNA polymerase B srb9 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9HE02"}


id: GO:0021878
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into an astrocyte that resides in the forebrain.","definition_xrefs":["GOC:dgh","GOC:cls","GO_REF:0000021","GOC:dph","GOC:jid","PMID:16226447"],"direct_ancestors":[{"relation_name":"is_a","term_name":"astrocyte fate commitment","termid":"GO:0060018"},{"relation_name":"part_of","term_name":"forebrain astrocyte differentiation","termid":"GO:0021896"}],"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":"forebrain astrocyte fate commitment","termid":"GO:0021878"}


id: PBO:0001309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF726 family protein","termid":"PBO:0001309"}


id: GO:0050921
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the directed movement of a motile cell or organism in response to a specific chemical concentration gradient.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to external stimulus","termid":"GO:0032103"},{"relation_name":"is_a","term_name":"positive regulation of locomotion","termid":"GO:0040017"},{"relation_name":"is_a","term_name":"regulation of chemotaxis","termid":"GO:0050920"},{"relation_name":"positively_regulates","term_name":"chemotaxis","termid":"GO:0006935"}],"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 chemotaxis","synonyms":[{"name":"activation of chemotaxis","type":"narrow"},{"name":"stimulation of chemotaxis","type":"narrow"},{"name":"up regulation of chemotaxis","type":"exact"},{"name":"up-regulation of chemotaxis","type":"exact"},{"name":"upregulation of chemotaxis","type":"exact"}],"termid":"GO:0050921"}


id: GO:0090256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of the multiplication or reproduction of cells, resulting in the expansion of a cell population that contributes to imaginal disc-derived wing morphogenesis.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell population proliferation","termid":"GO:0042127"},{"relation_name":"is_a","term_name":"regulation of post-embryonic development","termid":"GO:0048580"},{"relation_name":"part_of","term_name":"imaginal disc-derived wing morphogenesis","termid":"GO:0007476"},{"relation_name":"regulates","term_name":"cell proliferation involved in imaginal disc-derived wing morphogenesis","termid":"GO:0090255"}],"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 cell proliferation involved in imaginal disc-derived wing morphogenesis","termid":"GO:0090256"}


id: PBO:0065202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRPF31 antisense RNA 1","termid":"PBO:0065202"}


id: PBO:0060569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBPF member 5, pseudogene","termid":"PBO:0060569"}


id: GO:1903784
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of sodium ion import across the plasma membrane.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:mtg_cardiac_conduct_nov11","PMID:19376779","GOC:BHF","GOC:nc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of sodium ion transmembrane transport","termid":"GO:1902307"},{"relation_name":"is_a","term_name":"regulation of sodium ion import across plasma membrane","termid":"GO:1903782"},{"relation_name":"positively_regulates","term_name":"sodium ion import across plasma membrane","termid":"GO:0098719"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"positive regulation of sodium ion import across plasma membrane","synonyms":[{"name":"activation of sodium ion import across plasma membrane","type":"narrow"},{"name":"up regulation of sodium ion import across plasma membrane","type":"exact"},{"name":"up-regulation of sodium ion import across plasma membrane","type":"exact"},{"name":"upregulation of sodium ion import across plasma membrane","type":"exact"}],"termid":"GO:1903784"}


id: GO:0097525
data:
  {"annotated_genes":["SJAG_00147","SJAG_03460","SJAG_04214","SJAG_04222","SJAG_03214","SJAG_01819","SJAG_01634","SJAG_01547","SJAG_01008","SJAG_00504","SJAG_04433","SJAG_03410","SJAG_00058","SJAG_02295","SJAG_00643","SJAG_01452","SJAG_00539","SJAG_01327","SJAG_00278","SJAG_05009","SJAG_03369","SJAG_03995","SJAG_02304","SJAG_04230","SJAG_03210","SJAG_00989","SJAG_05240","SJAG_04163","SJAG_02185","SJAG_02455","SJAG_01440","SJAG_03070","SJAG_04911","SJAG_00577","SJAG_03469","SJAG_01301","SJAG_00414","SJAG_02843","SJAG_02279","SJAG_02469","SJAG_05208","SJAG_01654","SJAG_01308","SJAG_03954","SJAG_03245","SJAG_04079","SJAG_00322","SJAG_04497","SJAG_03983","SJAG_04529","SJAG_01870","SJAG_01015","SJAG_00474","SJAG_00498","SJAG_00313","SJAG_04405","SJAG_03547","SJAG_05235","SJAG_04318","SJAG_00531","SJAG_04538"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70233,79323,76792,112112,113020,79147,72502,75419,69839,106699,72913,76595,76488,73808,102461,93762,73853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005685"},{"annotations":[77476,116143,76793,109252,72503,102164,108289,75567,73668,107639,79148,109816,71934,75191,114677,76489,115609,112627,73026,102956,77158,75420,112400,95578,80070,75765,70149,73749,70234,106101],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005686"},{"annotations":[74859,72504,76794,70235,76490,79149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005687"},{"annotations":[78267,105638,77225,78567,70236,110887,71284,75422,116145,105596,110376,61883,78104,100388,77249,63155,109817,70450,79012,92880,97766,72506,77146,74021,76073,108290,94938,79809,114603,77112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046540"},{"annotations":[102457,108291,97157,109818,115611,95580,117571,72501,70232,75948,106304,114679,116146,77111,79146,76791,75418,78266,76487,100389,112629,106103,72248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005682"},{"annotations":[70449,61882,71494,78566,79807,77224,78675,105251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005688"}]},"cv_name":"cellular_component","definition":"A small ribonucleoprotein complex involved in formation of the spliceosome.","definition_xrefs":["ISBN:0879695897","GOC:krc","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small nuclear ribonucleoprotein complex","termid":"GO:0030532"}],"gene_count":61,"genes_by_uniquename":{"SJAG_00058":null,"SJAG_00147":null,"SJAG_00278":null,"SJAG_00313":null,"SJAG_00322":null,"SJAG_00414":null,"SJAG_00474":null,"SJAG_00498":null,"SJAG_00504":null,"SJAG_00531":null,"SJAG_00539":null,"SJAG_00577":null,"SJAG_00643":null,"SJAG_00989":null,"SJAG_01008":null,"SJAG_01015":null,"SJAG_01301":null,"SJAG_01308":null,"SJAG_01327":null,"SJAG_01440":null,"SJAG_01452":null,"SJAG_01547":null,"SJAG_01634":null,"SJAG_01654":null,"SJAG_01819":null,"SJAG_01870":null,"SJAG_02185":null,"SJAG_02279":null,"SJAG_02295":null,"SJAG_02304":null,"SJAG_02455":null,"SJAG_02469":null,"SJAG_02843":null,"SJAG_03070":null,"SJAG_03210":null,"SJAG_03214":null,"SJAG_03245":null,"SJAG_03369":null,"SJAG_03410":null,"SJAG_03460":null,"SJAG_03469":null,"SJAG_03547":null,"SJAG_03954":null,"SJAG_03983":null,"SJAG_03995":null,"SJAG_04079":null,"SJAG_04163":null,"SJAG_04214":null,"SJAG_04222":null,"SJAG_04230":null,"SJAG_04318":null,"SJAG_04405":null,"SJAG_04433":null,"SJAG_04497":null,"SJAG_04529":null,"SJAG_04538":null,"SJAG_04911":null,"SJAG_05009":null,"SJAG_05208":null,"SJAG_05235":null,"SJAG_05240":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"spliceosomal snRNP complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0097525","terms_by_termid":{"GO:0005682":null,"GO:0005685":null,"GO:0005686":null,"GO:0005687":null,"GO:0005688":null,"GO:0046540":null}}


id: PBO:0030387
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cell_cortex_morphology_during_nitrogen_starvation","termid":"PBO:0030387"}


id: GO:0014737
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of muscle atrophy.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle atrophy","termid":"GO:0014735"},{"relation_name":"is_a","term_name":"positive regulation of muscle adaptation","termid":"GO:0014744"},{"relation_name":"positively_regulates","term_name":"muscle atrophy","termid":"GO:0014889"}],"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 muscle atrophy","termid":"GO:0014737"}


id: GO:0014068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of signal transduction mediated by the phosphatidylinositol 3-kinase cascade.","definition_xrefs":["GOC:ef"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of phosphatidylinositol 3-kinase signaling (obsolete GO:0014068)","synonyms":[{"name":"activation of phosphoinositide 3-kinase cascade","type":"narrow"},{"name":"positive regulation of PI 3-kinase cascade","type":"exact"},{"name":"positive regulation of PI3K cascade","type":"exact"},{"name":"positive regulation of phosphatidylinositol 3-kinase cascade","type":"related"},{"name":"positive regulation of phosphoinositide 3-kinase cascade","type":"exact"},{"name":"stimulation of phosphatidylinositol 3-kinase cascade","type":"narrow"},{"name":"up regulation of phosphatidylinositol 3-kinase cascade","type":"exact"},{"name":"up-regulation of phosphatidylinositol 3-kinase cascade","type":"exact"},{"name":"upregulation of phosphatidylinositol 3-kinase cascade","type":"exact"}],"termid":"GO:0014068"}


id: PBO:0044991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DExH-box helicase 58","termid":"PBO:0044991"}


id: GO:0010387
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a COP9 signalosome.","definition_xrefs":["PMID:17307927"],"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":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"COP9 signalosome assembly","synonyms":[{"name":"signalosome assembly","type":"broad"}],"termid":"GO:0010387"}


id: GO:0042461
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Development of a photoreceptor, a cell that responds to incident electromagnetic radiation, particularly visible light.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron development","termid":"GO:0048666"},{"relation_name":"part_of","term_name":"photoreceptor cell differentiation","termid":"GO:0046530"}],"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":"photoreceptor cell development","secondary_identifiers":["GO:0046531"],"synonyms":[{"name":"photoreceptor morphogenesis","type":"exact"}],"termid":"GO:0042461"}


id: MONDO:0015993
data:
  {"annotated_genes":["SJAG_01897","SJAG_04225"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014372"},{"annotations":[84860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014669"}]},"cv_name":"mondo","definition":"Inherited retinal dystrophies that belong to the group of pigmentary retinopathies.","definition_xrefs":["Orphanet:1872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01897":null,"SJAG_04225":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cone-rod dystrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:120970","GARD:10790","ICD10CM:H35.5","MESH:D000071700","UMLS:C4085590","MEDGEN:896366","DOID:0050572","NANDO:1200937"],"synonyms":[{"name":"CRD","type":"exact"},{"name":"cone rod dystrophy","type":"related"},{"name":"cone-rod retinal dystrophy","type":"exact"}],"termid":"MONDO:0015993","terms_by_termid":{"MONDO:0014372":null,"MONDO:0014669":null},"xrefs":{"Monarch":{"xref_id":"0015993"}}}


id: PBO:0040210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASXL transcriptional regulator 3","termid":"PBO:0040210"}


id: PBO:0050670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSPA5 pseudogene 1","termid":"PBO:0050670"}


id: GO:0040004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Attaching of a collagen and cuticulin-based cuticle to the epithelium underlying it. An example of this process is found in Caenorhabditis elegans.","definition_xrefs":["GOC:ems","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molting cycle process","termid":"GO:0022404"},{"relation_name":"part_of","term_name":"molting cycle, collagen and cuticulin-based cuticle","termid":"GO:0018996"}],"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":"collagen and cuticulin-based cuticle attachment to epithelium","synonyms":[{"name":"cuticular attachment to epithelium","type":"broad"}],"termid":"GO:0040004"}


id: GO:0044397
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process of actin cortical patch localization in which the patch moves from the cell surface to the inside of the cell.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete actin cortical patch internalization (obsolete GO:0044397)","termid":"GO:0044397"}


id: GO:0005764
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small lytic vacuole that has cell cycle-independent morphology found in most animal cells and that contains a variety of hydrolases, most of which have their maximal activities in the pH range 5-6. The contained enzymes display latency if properly isolated. About 40 different lysosomal hydrolases are known and lysosomes have a great variety of morphologies and functions.","definition_xrefs":["ISBN:0198506732","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lytic vacuole","termid":"GO:0000323"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005773"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005773"],"is_obsolete":false,"name":"lysosome","secondary_identifiers":["NIF_Subcellular:sao585356902","Wikipedia:Lysosome"],"termid":"GO:0005764"}


id: PBO:0058598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6730","termid":"PBO:0058598"}


id: PBO:0067023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 36, pseudogene","termid":"PBO:0067023"}


id: GO:0006904
data:
  {"annotated_genes":["SJAG_03499","SJAG_02587","SJAG_00280","SJAG_01697","SJAG_02320","SJAG_03005","SJAG_01772","SJAG_04966"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60168,69530,74744,79579,79883,90341,92096,117957],"is_not":false,"summary":null,"term":"GO:0006904"}]},"cv_name":"biological_process","definition":"The initial attachment of a vesicle membrane to a target membrane, mediated by proteins protruding from the membrane of the vesicle and the target membrane, that contributes to exocytosis.","definition_xrefs":["GOC:bc","GOC:jid","PMID:22438915","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle docking","termid":"GO:0048278"},{"relation_name":"is_a","term_name":"exocytic process","termid":"GO:0140029"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00280":null,"SJAG_01697":null,"SJAG_01772":null,"SJAG_02320":null,"SJAG_02587":null,"SJAG_03005":null,"SJAG_03499":null,"SJAG_04966":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0140056"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0140056","GO:0051179","GO:0016192"],"is_obsolete":false,"name":"vesicle docking involved in exocytosis","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"vesicle docking during exocytosis","type":"related"}],"termid":"GO:0006904","terms_by_termid":{"GO:0006904":null}}


id: MONDO:0957919
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"Lui-Jee-Baron syndrome","secondary_identifiers":["OMIM:301114","MEDGEN:1849943","UMLS:C5882664"],"termid":"MONDO:0957919","xrefs":{"Monarch":{"xref_id":"0957919"}}}


id: PBO:0034235
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-involved_in_positive_regulation_of","termid":"PBO:0034235"}


id: PBO:0057955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3678","termid":"PBO:0057955"}


id: GO:0018768
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,4E)-6-(2-aminophenyl)-2-hydroxy-6-oxohexa-2,4-dienoate + H2O = (2E)-2-hydroxypenta-2,4-dienoate + anthranilate + H+.","definition_xrefs":["RHEA:27870"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances","termid":"GO:0016823"}],"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:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"2-hydroxy-6-oxo-6-(2'-aminophenyl)hexa-2,4-dienoate hydrolase activity","secondary_identifiers":["EC:3.7.1.13","MetaCyc:RXN-11543","UM-BBD_reactionID:r0458"],"termid":"GO:0018768"}


id: MONDO:1010882
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lysosomal storage disease in springboks. There is a buildup of GM2 gangliosides in tissues due to the lack of the enzyme hexosaminidase.","definition_xrefs":["PMID:25232033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gangliosidosis, non-human animal","termid":"MONDO:1010167"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GM2 gangliosidosis, springbok","secondary_identifiers":["OMIA:001462-59523"],"synonyms":[{"name":"gangliosidosis, GM2, type II (Sandhoff or variant 0), springbok","type":"related"}],"termid":"MONDO:1010882","xrefs":{"Monarch":{"xref_id":"1010882"}}}


id: GO:0010596
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of the orderly movement of an endothelial cell into the extracellular matrix to form an endothelium.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of endothelial cell migration","termid":"GO:0010594"},{"relation_name":"is_a","term_name":"negative regulation of cell migration","termid":"GO:0030336"},{"relation_name":"negatively_regulates","term_name":"endothelial cell migration","termid":"GO:0043542"}],"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 endothelial cell migration","termid":"GO:0010596"}


id: GO:0030143
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A vesicle that mediates transport of cargo within the Golgi complex (for example, between cisternae of the Golgi stack).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport vesicle","termid":"GO:0030133"},{"relation_name":"is_a","term_name":"COPI-coated vesicle","termid":"GO:0030137"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0031410","GO:0005575"],"is_obsolete":false,"name":"COPI-coated inter-Golgi transport vesicle","secondary_identifiers":["GO:0005807","NIF_Subcellular:sao1382918459"],"synonyms":[{"name":"inter-Golgi transport constitutive secretory pathway transport vesicle","type":"exact"}],"termid":"GO:0030143"}


id: PBO:0067332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 424, pseudogene","termid":"PBO:0067332"}


id: MONDO:0018283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary qualitative or quantitative defects of alpha-dystroglycan (obsolete MONDO:0018283)","secondary_identifiers":["Orphanet:371040"],"synonyms":[{"name":"primary alpha-dystroglycanopathy","type":"exact"},{"name":"primary dystroglycanopathy","type":"exact"}],"termid":"MONDO:0018283","xrefs":{"Monarch":{"xref_id":"0018283"}}}


id: PBO:0074312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMAD3 antisense RNA 1","termid":"PBO:0074312"}


id: GO:0004953
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an icosanoid to initiate a change in cell activity.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"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":"icosanoid receptor activity","synonyms":[{"name":"eicosanoid receptor activity","type":"exact"}],"termid":"GO:0004953"}


id: GO:0018307
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of part of an enzyme to form the active site.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete enzyme active site formation (obsolete GO:0018307)","termid":"GO:0018307"}


id: GO:0047212
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: trans-2-coumarate + UDP-D-glucose = trans-beta-D-glucosyl-2-hydroxycinnamate + H+ + UDP.","definition_xrefs":["RHEA:10236","EC:2.4.1.114"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016757","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"2-coumarate O-beta-glucosyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.114-RXN","KEGG_REACTION:R03710"],"synonyms":[{"name":"UDP-glucose:trans-2-hydroxycinnamate O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPG:o-coumaric acid O-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:trans-2-hydroxycinnamate O-beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-o-coumarate glucosyltransferase activity","type":"related"}],"termid":"GO:0047212"}


id: PBO:0001430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LEM domain","termid":"PBO:0001430"}


id: MOD:01319
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other","definition_xrefs":["PubMed:11510821","PubMed:9448752","Unimod:176#H","PubMed:12422359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Michael addition of BHT quinone methide to cysteine and lysine","termid":"MOD:00534"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Michael addition of BHT quinone methide to histidine","synonyms":[{"name":"BHT","type":"related"},{"name":"Michael addition of BHT quinone methide to Cysteine and Lysine","type":"related"}],"termid":"MOD:01319"}


id: PBO:0002598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk2 (predicted)","termid":"PBO:0002598"}


id: PBO:0048138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FXYD domain containing ion transport regulator 2","termid":"PBO:0048138"}


id: MONDO:0015867
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma arising from the vaginal epithelium. The majority of vaginal carcinomas are squamous cell carcinomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal cancer","termid":"MONDO:0001402"},{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"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":"vaginal carcinoma","secondary_identifiers":["GARD:9348","Orphanet:180247","DOID:0050918","UMLS:C0262659","MEDGEN:82653","NCIT:C3917"],"synonyms":[{"name":"cancer of the vagina","type":"broad"},{"name":"cancer of vagina","type":"broad"},{"name":"carcinoma of the vagina","type":"exact"},{"name":"carcinoma of vagina","type":"exact"},{"name":"vagina cancer","type":"broad"},{"name":"vagina carcinoma","type":"exact"},{"name":"vaginal cancer","type":"broad"},{"name":"vaginal cancer, NOS","type":"broad"},{"name":"vaginal carcinoma","type":"exact"},{"name":"vaginal malignant epithelial tumor","type":"broad"},{"name":"vaginal malignant epithelial tumour","type":"broad"}],"termid":"MONDO:0015867","xrefs":{"Monarch":{"xref_id":"0015867"}}}


id: MONDO:0008667
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A familial cancer predisposition syndrome associated with a variety of malignant and benign neoplasms, most frequently retinal, cerebellar, and spinal hemangioblastoma, renal cell carcinoma (RCC), and pheochromocytoma.","definition_xrefs":["Orphanet:892"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"excluded_subClassOf","term_name":"multiple polyglandular tumor","termid":"MONDO:0015079"},{"relation_name":"excluded_subClassOf","term_name":"obsolete genetic central nervous system and retinal vascular disease (obsolete MONDO:0015953)","termid":"MONDO:0015953"},{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited nervous system cancer-predisposing syndrome (obsolete MONDO:0016756)","termid":"MONDO:0016756"},{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited renal cancer-predisposing syndrome (obsolete MONDO:0017891)","termid":"MONDO:0017891"},{"relation_name":"excluded_subClassOf","term_name":"familial cystic renal disease","termid":"MONDO:0019741"},{"relation_name":"excluded_subClassOf","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"excluded_subClassOf","term_name":"obsolete disorder of central nervous system or retinal vasculature (obsolete MONDO:0020676)","termid":"MONDO:0020676"},{"relation_name":"excluded_subClassOf","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"neurocutaneous syndrome","termid":"MONDO:0042983"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"von Hippel-Lindau disease","secondary_identifiers":["OMIM:193300","UMLS:C0019562","ICD9:759.6","SCTID:46659004","DOID:14175","NANDO:2200408","MedDRA:10047716","NANDO:2200829","MESH:D006623","GARD:7855","icd11.foundation:1985408165","NORD:1830","MEDGEN:42458","NCIT:C3105"],"synonyms":[{"name":"Hippel Lindau syndrome","type":"exact"},{"name":"Lindau disease","type":"exact"},{"name":"VHL","type":"exact"},{"name":"VHL syndrome","type":"related"},{"name":"Von Hippel Lindau disease","type":"related"},{"name":"Von Hippel-Lindau syndrome","type":"exact"},{"name":"Von Hippel-Lindau syndrome (VHL)","type":"exact"},{"name":"Von Hippel-Lindau syndrome, Modifiers of","type":"related"},{"name":"cerebroretinal angiomatosis","type":"exact"},{"name":"familial cerebelloretinal angiomatosis","type":"exact"},{"name":"von Hippel-Lindau disease","type":"exact"},{"name":"von Hippel-Lindau syndrome","type":"exact"},{"name":"von Hippel-Lindau syndrome, modifier of","type":"exact"}],"termid":"MONDO:0008667","xrefs":{"Monarch":{"xref_id":"0008667"}}}


id: PR:000050502
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the dis1 gene in Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOG/XMAP215 microtubule plus end tracking polymerase Dis1 (Schizosaccharomyces pombe)","pombase_gene_id":"SPCC736.14","synonyms":[{"name":"SPCC736.14","type":"related"},{"name":"Spom-dis1","type":"exact"},{"name":"dis1","type":"related"},{"name":"phosphoprotein p99","type":"exact"}],"termid":"PR:000050502"}


id: PBO:0087681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the mitochondrial (mt) i-AAA protease supercomplex; i-AAA degrades misfolded mitochondrial proteins; forms a subcomplex with Mgr3p that binds to substrates to facilitate proteolysis; required for growth of cells lacking mtDNA","termid":"PBO:0087681"}


id: GO:0038095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of the Fc portion of immunoglobulin E (IgE) to an Fc-epsilon receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription. The Fc portion of an immunoglobulin is its C-terminal constant region.","definition_xrefs":["PMID:12413516","GOC:phg","PMID:15048725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fc receptor signaling pathway","termid":"GO:0038093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"Fc-epsilon receptor signaling pathway","secondary_identifiers":["Reactome:R-HSA-2454202"],"synonyms":[{"name":"Fc-epsilon receptor signalling pathway","type":"exact"}],"termid":"GO:0038095"}


id: PATO:0001977
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's having at least one salient angle on the margin.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angular","synonyms":[{"name":"angulate","type":"exact"}],"termid":"PATO:0001977"}


id: PBO:0064172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group VI","termid":"PBO:0064172"}


id: PATO:0002204
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Handedness where the organism exhibits no overall dominance in the use of right or left hand or foot in the performance of tasks that require one hand or foot or a dominant hand or foot.","definition_xrefs":["birnlex:2042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"handedness","termid":"PATO:0002201"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ambidextrous handedness","termid":"PATO:0002204"}


id: PBO:0066716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 13","termid":"PBO:0066716"}


id: PBO:0038734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin like 7A","termid":"PBO:0038734"}


id: PBO:0055424
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 2854","termid":"PBO:0055424"}


id: PBO:0053093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"late cornified envelope 3A","termid":"PBO:0053093"}


id: PBO:0084359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Leucyl aminopeptidase yscIV with epoxide hydrolase activity; metalloenzyme containing one zinc atom; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus; also known as leukotriene A4 hydrolase","termid":"PBO:0084359"}


id: GO:0047301
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-methyl-2-oxopentanoate + L-valine = 3-methyl-2-oxobutanoate + L-isoleucine.","definition_xrefs":["EC:2.6.1.32","RHEA:11468"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016769","GO:0003824"],"is_obsolete":false,"name":"valine-3-methyl-2-oxovalerate transaminase activity","secondary_identifiers":["KEGG_REACTION:R02200","MetaCyc:2.6.1.32-RXN"],"synonyms":[{"name":"L-valine:(S)-3-methyl-2-oxopentanoate aminotransferase activity","type":"related"},{"name":"valine--3-methyl-2-oxovalerate aminotransferase activity","type":"related"},{"name":"valine--isoleucine aminotransferase activity","type":"related"},{"name":"valine--isoleucine transaminase activity","type":"related"},{"name":"valine-2-keto-methylvalerate aminotransferase activity","type":"related"},{"name":"valine-3-methyl-2-oxovalerate aminotransferase activity","type":"exact"}],"termid":"GO:0047301"}


id: MONDO:0014653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the ZNF408 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 72","secondary_identifiers":["MEDGEN:895867","UMLS:C4225315","GARD:16119","DOID:0110395","ICD10CM:H35.5","OMIM:616469"],"synonyms":[{"name":"RP72","type":"exact"},{"name":"ZNF408 retinitis pigmentosa","type":"exact"},{"name":"retinitis pigmentosa 72","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in ZNF408","type":"exact"},{"name":"retinitis pigmentosa type 72","type":"exact"}],"termid":"MONDO:0014653","xrefs":{"Monarch":{"xref_id":"0014653"}}}


id: PBO:0112955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rnacentral_2d_structure_id","termid":"PBO:0112955"}


id: MONDO:0005353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. The excessive use of marijuana with associated psychological symptoms and impairment in social or occupational functioning.","definition_xrefs":["EFO:0004218"],"gene_count":0,"genotype_count":0,"name":"obsolete marijuana dependence (obsolete MONDO:0005353)","termid":"MONDO:0005353","xrefs":{"Monarch":{"xref_id":"0005353"}}}


id: MONDO:0800424
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colorectal cancer, susceptibility to, on chromosome 15","secondary_identifiers":["MEDGEN:394249","UMLS:C2677291"],"termid":"MONDO:0800424","xrefs":{"Monarch":{"xref_id":"0800424"}}}


id: PBO:0081159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFPM2 antisense RNA 1","termid":"PBO:0081159"}


id: PBO:0078355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 2-1","termid":"PBO:0078355"}


id: MOD:00773
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Natural or modified residues with a mass of 181.00-181.02 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at a resolution below 0.01 Da","termid":"MOD:00770"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"residues isobaric at 181.00-181.02 Da","termid":"MOD:00773"}


id: PBO:0001284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Ebp2 (predicted)","termid":"PBO:0001284"}


id: GO:0086065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates interactions between a cell and its surroundings that contributes to the process of cardiac conduction. Encompasses interactions such as signaling or attachment between one cell and another cell, between a cell and an extracellular matrix, or between a cell and any other aspect of its environment.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell communication","termid":"GO:0007154"},{"relation_name":"part_of","term_name":"cardiac conduction","termid":"GO:0061337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell communication involved in cardiac conduction","termid":"GO:0086065"}


id: MONDO:0006807
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rupture in the wall of the small or large intestine due to traumatic or pathologic processes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"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":"intestinal perforation","secondary_identifiers":["DOID:2074","MEDGEN:9525","ICD9:569.83","EFO:1000987","MESH:D007416","ICD9:777.6","MedDRA:10022694","SCTID:56905009","UMLS:C0021845","NCIT:C39611"],"synonyms":[{"name":"bowel perforation","type":"exact"},{"name":"perforation of intestine","type":"exact"}],"termid":"MONDO:0006807","xrefs":{"Monarch":{"xref_id":"0006807"}}}


id: MONDO:0004613
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ischemia of the intestine that is rapid in onset.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ischemic bowel disorder","termid":"MONDO:0020675"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"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":"acute intestinal ischemia","secondary_identifiers":["MEDGEN:116","SCTID:91489000","ICD9:557.0","NCIT:C34356","DOID:8590","UMLS:C0001363"],"synonyms":[{"name":"acute intestinal ischemia","type":"exact"},{"name":"acute intestinal vascular insufficiency","type":"narrow"}],"termid":"MONDO:0004613","xrefs":{"Monarch":{"xref_id":"0004613"}}}


id: GO:0090060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of metaxylem development. Metaxylem development is the process whose specific outcome is the progression of the metaxylem over time, from its formation to the mature structure. The metaxylem is the part of the primary xylem that differentiates after the protoxylem and before the secondary xylem, if any of the latter is formed.","definition_xrefs":["GOC:dph","GOC:sdb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal development","termid":"GO:2000026"},{"relation_name":"regulates","term_name":"metaxylem development","termid":"GO:0090058"}],"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 metaxylem development","termid":"GO:0090060"}


id: GO:0004412
data:
  {"annotated_genes":["SJAG_03152"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70886],"is_not":false,"summary":null,"term":"GO:0004412"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-homoserine + NADP+ = L-aspartate-4-semialdehyde + NADPH + H+.","definition_xrefs":["EC:1.1.1.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03152":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"homoserine dehydrogenase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:15761","MetaCyc:HOMOSERDEHYDROG-RXN"],"termid":"GO:0004412","terms_by_termid":{"GO:0004412":null}}


id: MONDO:0001758
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant soft tissue neoplasm that arises from the paranasal sinus.","definition_xrefs":["NCIT:C6849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paranasal sinus carcinoma","termid":"MONDO:0000380"},{"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":"paranasal sinus sarcoma","secondary_identifiers":["DOID:1362","UMLS:C1335342","MEDGEN:233842"],"synonyms":[{"name":"accessory sinus sarcoma","type":"exact"},{"name":"paranasal sinus sarcoma","type":"exact"},{"name":"sarcoma of accessory sinus","type":"exact"},{"name":"sarcoma of paranasal sinus","type":"exact"},{"name":"sarcoma of the accessory sinus","type":"exact"},{"name":"sarcoma of the paranasal sinus","type":"exact"}],"termid":"MONDO:0001758","xrefs":{"Monarch":{"xref_id":"0001758"}}}


id: PBO:0029639
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_TPCK","termid":"PBO:0029639"}


id: GO:0048337
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mesoderm cell fate specification.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell fate specification","termid":"GO:0042660"},{"relation_name":"is_a","term_name":"regulation of mesodermal cell fate specification","termid":"GO:0042661"},{"relation_name":"is_a","term_name":"positive regulation of mesodermal cell differentiation","termid":"GO:1905772"},{"relation_name":"positively_regulates","term_name":"mesodermal cell fate specification","termid":"GO:0007501"}],"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 mesodermal cell fate specification","synonyms":[{"name":"activation of mesodermal cell fate specification","type":"narrow"},{"name":"stimulation of mesodermal cell fate specification","type":"narrow"},{"name":"up regulation of mesodermal cell fate specification","type":"exact"},{"name":"up-regulation of mesodermal cell fate specification","type":"exact"},{"name":"upregulation of mesodermal cell fate specification","type":"exact"}],"termid":"GO:0048337"}


id: RO:0002437
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"An interaction relationship in which at least one of the partners is an organism and the other is either an organism or an abiotic entity with which the organism interacts.","direct_ancestors":[{"relation_name":"is_a","term_name":"ecologically_related_to","termid":"RO:0002321"},{"relation_name":"is_a","term_name":"interacts_with","termid":"RO:0002434"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"biotically_interacts_with","termid":"RO:0002437"}


id: PBO:0000148
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"divergent duplication","termid":"PBO:0000148"}


id: GO:0030089
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any of the granules, approximately 32 nm x 48 nm and consisting of highly aggregated phycobiliproteins, that are attached in arrays to the external face of a thylakoid membrane in algae of the phyla Cyanophyta and Rhodophyta, where they function as light-harvesting devices in photosynthesis. Excitation energy in the phycobilisome flows in the sequence: phycoerythrin, phycocyanin, allophycocyanin before passing to the antenna chlorophyll of photosystem II.","definition_xrefs":["Wikipedia:Phycobilisome","GOC:jl","PMID:11734882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"light-harvesting complex","termid":"GO:0030076"},{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"thylakoid membrane","termid":"GO:0042651"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"phycobilisome","termid":"GO:0030089"}


id: MONDO:0010350
data:
  {"annotated_genes":["SJAG_04703"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86778],"is_not":false,"summary":null,"term":"MONDO:0010350"}]},"cv_name":"mondo","definition":"Any primary ovarian failure in which the cause of the disease is a mutation in the DIAPH2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04703":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"premature ovarian failure 2A","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080858","MEDGEN:336902","MESH:C564498","OMIM:300511","UMLS:C1845293"],"synonyms":[{"name":"DIAPH2 primary ovarian failure","type":"exact"},{"name":"POF2A","type":"related"},{"name":"premature ovarian failure 2A","type":"exact"},{"name":"premature ovarian failure 2A, X-linked dominant","type":"exact"},{"name":"premature ovarian failure type 2A","type":"exact"},{"name":"primary ovarian failure caused by mutation in DIAPH2","type":"exact"}],"termid":"MONDO:0010350","terms_by_termid":{"MONDO:0010350":null},"xrefs":{"Monarch":{"xref_id":"0010350"}}}


id: GO:0043858
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: arginine(out) + ornithine(in) = arginine(in) + ornithine(out).","definition_xrefs":["GOC:jl","PMID:17110979","RHEA:34991"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"amino acid transmembrane transporter activity","termid":"GO:0015171"},{"relation_name":"is_a","term_name":"antiporter activity","termid":"GO:0015297"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"arginine:ornithine antiporter activity","synonyms":[{"name":"ArcD","type":"related"},{"name":"arginine-ornithine antiporter activity","type":"exact"},{"name":"arginine/ornithine antiporter activity","type":"exact"}],"termid":"GO:0043858"}


id: PBO:0113485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"This gene is absent from the reference genome, but present in various other strains' genomes; similar to MAL63","termid":"PBO:0113485"}


id: PBO:0047674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fli-1 proto-oncogene, ETS transcription factor","termid":"PBO:0047674"}


id: PBO:0091614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminotransferase class-III, possible transaminase, unknown specificity, implicated in amino acid or cofactor metabolism","termid":"PBO:0091614"}


id: GO:0022809
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Small molecule produced by bacteria that carries an ion across the membrane by enclosing the ion and travelling with the ion across the membrane. It does not form a fully open pore across the membrane.","definition_xrefs":["GOC:pr","ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"mobile ion carrier activity","synonyms":[{"name":"ionophore","type":"broad"}],"termid":"GO:0022809"}


id: PBO:0113751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tudor domain superfamily protein, potential role in central carbon metabolism based on C. neoformans metabolic data, see PF11160","termid":"PBO:0113751"}


id: MONDO:1011785
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease, non-human animal","termid":"MONDO:1011360"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lethal multi-organ developmental dysplasia, non-human animal","secondary_identifiers":["OMIA:001722"],"termid":"MONDO:1011785","xrefs":{"Monarch":{"xref_id":"1011785"}}}


id: MONDO:0003849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A slow-growing malignant bone tumor arising from the remnants of the notochord and occurring in the clivus. It is characterized by a lobulated growth pattern, myxoid stroma formation, and the presence of physaliphorous cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skull base chordoma","termid":"MONDO:0002892"}],"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":"clivus chordoma","secondary_identifiers":["NCIT:C5412","DOID:6312","SCTID:446939001","ICD9:170.0","MEDGEN:232372","UMLS:C1333071"],"synonyms":[{"name":"chordoma (disease) of clivus of occipital bone","type":"exact"},{"name":"chordoma of clivus","type":"exact"},{"name":"chordoma of the clivus","type":"exact"},{"name":"clival chordoma","type":"exact"},{"name":"clivus of occipital bone chordoma (disease)","type":"exact"}],"termid":"MONDO:0003849","xrefs":{"Monarch":{"xref_id":"0003849"}}}


id: PBO:0044751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DExD-box helicase 39A","termid":"PBO:0044751"}


id: MONDO:0008136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary optic neuropathy","termid":"MONDO:0020249"},{"relation_name":"is_a","term_name":"PAX6-related ocular dysgenesis","termid":"MONDO:0800183"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005240","MONDO:0005328"],"is_obsolete":false,"name":"isolated optic nerve hypoplasia","secondary_identifiers":["DOID:0111531","icd11.foundation:609162974","NORD:1528","OMIM:165550","MEDGEN:322281","GARD:8419","Orphanet:137902","Orphanet:637061","SCTID:724999003","UMLS:C1833797"],"synonyms":[{"name":"Optic Nerve Hypoplasia","type":"exact"},{"name":"familial bilateral optic nerve hypoplasia","type":"exact"},{"name":"isolated optic nerve hypoplasia/aplasia","type":"related"},{"name":"optic nerve aplasia, bilateral","type":"related"},{"name":"optic nerve hypoplasia","type":"related"},{"name":"optic nerve hypoplasia, bilateral","type":"exact"},{"name":"optic nerve hypoplasia, familial bilateral","type":"exact"}],"termid":"MONDO:0008136","xrefs":{"Monarch":{"xref_id":"0008136"}}}


id: PBO:0051252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (III)-13-1 (pseudogene)","termid":"PBO:0051252"}


id: MONDO:0044717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 4","termid":"MONDO:0016903"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4q25 proximal deletion syndrome","secondary_identifiers":["MEDGEN:1814447","UMLS:C5680087","Orphanet:502437","GARD:22048"],"synonyms":[{"name":"proximal del(4)(q25)","type":"exact"},{"name":"proximal monosomy 4q25","type":"exact"}],"termid":"MONDO:0044717","xrefs":{"Monarch":{"xref_id":"0044717"}}}


id: PBO:0084890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial translational activator of the COB mRNA; interacts with translating ribosomes, acts on the COB mRNA 5'-untranslated leader","termid":"PBO:0084890"}


id: PBO:0003704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MBF complex negative regulatory component Yox1","termid":"PBO:0003704"}


id: GO:0052534
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of induced systemic resistance in the symbiont organism; induced systemic resistance is a response that confers broad spectrum systemic resistance to disease and that does not depend upon salicylic acid signaling. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of induced systemic resistance in symbiont (obsolete GO:0052534)","synonyms":[{"name":"positive regulation by organism of induced systemic resistance in symbiont","type":"exact"}],"termid":"GO:0052534"}


id: GO:0044114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of an organism from an initial condition to a later condition, occurring within the cells or tissues of the host organism. This may (but not necessarily) include a filamentous growth form, and also can include secretion of proteases and lipases to break down host tissue. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:jl","GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formation of structure involved in a symbiotic process","termid":"GO:0044111"}],"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":"development of symbiont in host","secondary_identifiers":["GO:0044124","GO:0044122"],"synonyms":[{"name":"development of symbiont in host intercellular space","type":"narrow"},{"name":"development of symbiont in host vascular tissue","type":"narrow"}],"termid":"GO:0044114"}


id: GO:0035245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of a methyl group onto a carbon atom of an arginine residue in a protein.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-arginine C-methylation (obsolete GO:0035245)","termid":"GO:0035245"}


id: PBO:0060440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NACA pseudogene 9","termid":"PBO:0060440"}


id: PBO:0085238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peptidyl-prolyl cis/trans-isomerase; also activates the phosphotyrosyl phosphatase activity of protein phosphatase 2A (PP2A); regulates G1 phase progression, the osmoresponse, microtubule dynamics; subunit of the Tap42p-Pph21p-Rrd2p complex; protein abundance increases in response to DNA replication stress","termid":"PBO:0085238"}


id: GO:0047529
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2R,3S)-2,3-dimethylmalate = propanoate + pyruvate.","definition_xrefs":["RHEA:10472","EC:4.1.3.32"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxo-acid-lyase activity","termid":"GO:0016833"}],"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:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"2,3-dimethylmalate lyase activity","secondary_identifiers":["MetaCyc:23-DIMETHYLMALATE-LYASE-RXN","KEGG_REACTION:R01355"],"synonyms":[{"name":"(2R,3S)-2,3-dimethylmalate pyruvate-lyase (propanoate-forming)","type":"related"},{"name":"(2R,3S)-2,3-dimethylmalate pyruvate-lyase activity","type":"related"},{"name":"2,3-dimethylmalate pyruvate-lyase activity","type":"related"}],"termid":"GO:0047529"}


id: PR:O94538
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U4/U6.U5 tri-snRNP-associated protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00627","PRO:DNx","PANTHER:PTHR14152:SF5"],"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/U6.U5 tri-snRNP-associated protein snu66 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC167.03c","secondary_identifiers":["UniProtKB:O94538"],"synonyms":[{"name":"Spom972h-SART1","type":"exact"}],"termid":"PR:O94538"}


id: FYPO:0001768
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 posttranscriptional addition of methyl groups to the C38 residue in a tRNA-Asp molecule is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal tRNA methylation","termid":"FYPO:0001766"},{"relation_name":"is_a","term_name":"abolished tRNA modification","termid":"FYPO:0008344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0006551","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000294"],"is_obsolete":false,"name":"abolished tRNA-Asp C38 methylation","synonyms":[{"name":"abolished tRNA-Asp C38 methylation during mitotic cell cycle","type":"related"},{"name":"abolished tRNA-Asp C38 methylation during vegetative growth","type":"exact"},{"name":"abolished tRNA-Asp methylation on C38","type":"exact"},{"name":"tRNA-Asp C38 methylation abolished","type":"exact"}],"termid":"FYPO:0001768"}


id: GO:0043430
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-decaprenyl-6-methoxy-1,4-benzoquinone + S-adenosyl-L-methionine = 2-decaprenyl-3-methyl-6-methoxy-1,4-benzoquinone + S-adenosyl-L-homocysteine.","definition_xrefs":["PMID:11583838","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-decaprenyl-6-methoxy-1,4-benzoquinone methyltransferase activity (obsolete GO:0043430)","synonyms":[{"name":"2-decaprenyl-6-methoxy-1,4-benzoquinone methylase activity","type":"exact"}],"termid":"GO:0043430"}


id: PR:000050504
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A TOG/XMAP215 microtubule plus end tracking polymerase Dis1 that has not been phosphorylated at the positions equivalent to Thr-279, Ser-293, Ser-300, Ser-551, Ser-556, and Ser-590 of the amino acid sequence represented by UniProtKB:Q09933. Example: UniProtKB:Q09933, Thr-279/Ser-293/Ser-300/Ser-551/Ser-556/Ser-590, PR:000026291.","definition_xrefs":["PomBase:VW","PRO:DAN","PMID:16920624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TOG/XMAP215 microtubule plus end tracking polymerase Dis1 (Schizosaccharomyces pombe)","termid":"PR:000050502"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dis1/UnPhos(T279,S293,S300,S551,S556,S590)","pombase_gene_id":"SPCC736.14","synonyms":[{"name":"PomBase_original_PRO_term_name: TOG/XMAP215 microtubule plus end tracking polymerase Dis1 unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-dis1/UnPhos:1","type":"exact"},{"name":"UniProtKB:Q09933, Thr-279/Ser-293/Ser-300/Ser-551/Ser-556/Ser-590, PR:000026291","type":"narrow"},{"name":"dis1/UnPhos(T279,S293,S300,S551,S556,S590)","type":"exact"}],"termid":"PR:000050504"}


id: PBO:0029090
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_microtubule_bundle_formation","termid":"PBO:0029090"}


id: MONDO:0958184
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolytic ichthyosis","termid":"MONDO:0007239"}],"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":"epidermolytic hyperkeratosis 2","secondary_identifiers":["DOID:0081359"],"termid":"MONDO:0958184","xrefs":{"Monarch":{"xref_id":"0958184"}}}


id: PBO:0051543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 6 receptor pseudogene 1","termid":"PBO:0051543"}


id: GO:0014874
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. This occurs as part of the regulation of muscle adaptation.","definition_xrefs":["GOC:ef","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stimulus","termid":"GO:0050896"},{"relation_name":"part_of","term_name":"regulation of muscle adaptation","termid":"GO:0043502"}],"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 stimulus involved in regulation of muscle adaptation","synonyms":[{"name":"response to stimulus involved in regulation of muscle plasticity","type":"related"}],"termid":"GO:0014874"}


id: GO:0021806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial stages of cell motility involved in the glial-mediated movement of cells in the developing cerebral cortex.","definition_xrefs":["GOC:dph","GO_REF:0000021","PMID:12626695","GOC:jid","GOC:dgh","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"},{"relation_name":"part_of","term_name":"ameboidal-type cell migration","termid":"GO:0001667"},{"relation_name":"part_of","term_name":"cell motility involved in cerebral cortex radial glia guided migration","termid":"GO:0021814"}],"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":"initiation of movement involved in cerebral cortex radial glia guided migration","synonyms":[{"name":"initiation of movement involved in cerebral cortex glial-mediated radial migration","type":"related"}],"termid":"GO:0021806"}


id: PBO:0072994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCML2 pseudogene 1","termid":"PBO:0072994"}


id: MONDO:0016629
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hemorrhagic disorder due to a platelet anomaly (obsolete MONDO:0016629)","secondary_identifiers":["Orphanet:248326"],"synonyms":[{"name":"rare bleeding disorder due to a platelet anomaly","type":"exact"},{"name":"rare bleeding disorder due to a thrombopathy and/or thrombocytopenia","type":"exact"},{"name":"rare coagulopathy due to a platelet anomaly","type":"exact"},{"name":"rare coagulopathy due to a thrombopathy and/or thrombocytopenia","type":"exact"},{"name":"rare hemorrhagic disorder due to a thrombopathy and/or thrombocytopenia","type":"exact"}],"termid":"MONDO:0016629","xrefs":{"Monarch":{"xref_id":"0016629"}}}


id: PBO:0034792
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncertain translation start point","termid":"PBO:0034792"}


id: GO:1990477
data:
  {"annotated_genes":["SJAG_00701","SJAG_02382","SJAG_00456","SJAG_03939","SJAG_04768"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87251,90552,109007,111600,112498],"is_not":false,"summary":null,"term":"GO:1990477"}]},"cv_name":"cellular_component","definition":"Protein complex formed by an RNA binding protein Red1, an RNA helicase Mtl1, Red5, Rmn1, Iss10/Pir1, and Ars2/Pir2. This complex is required for the recruitment of the nuclear exosome to Mmi1 nuclear focus. It is likely related to the human CBCN complex. This complex is also known as RNA silencing (NURS) complex.","definition_xrefs":["PMID:24210919","PMID:32012158","PMID:24713849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00456":null,"SJAG_00701":null,"SJAG_02382":null,"SJAG_03939":null,"SJAG_04768":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"MTREC complex","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1990345"],"synonyms":[{"name":"Mtl1-Red1 core complex","type":"exact"},{"name":"NURS complex","type":"exact"},{"name":"PAXT complex","type":"exact"}],"termid":"GO:1990477","terms_by_termid":{"GO:1990477":null}}


id: PBO:0002210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminoadipate-semialdehyde dehydrogenase","termid":"PBO:0002210"}


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


id: PBO:0054727
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 2136","termid":"PBO:0054727"}


id: FYPO:0001260
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to hypoxia is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during vegetative growth","termid":"FYPO:0001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal RNA level during cellular response to hypoxia","synonyms":[{"name":"normal RNA accumulation during cellular response to hypoxia","type":"related"},{"name":"normal RNA level during cellular response to hyperoxic stress","type":"exact"},{"name":"normal RNA level during cellular response to hypoxia during mitotic cell cycle","type":"related"},{"name":"normal RNA level during cellular response to hypoxia during vegetative growth","type":"exact"},{"name":"normal RNA level during cellular response to increased oxygen tension","type":"exact"},{"name":"normal mRNA level during cellular response to hypoxia","type":"narrow"},{"name":"normal transcript level during cellular response to hypoxia","type":"exact"}],"termid":"FYPO:0001260"}


id: MONDO:1011486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Complement component 2 deficiency that occurs in domestic guinea pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complement component 2 deficiency, non-human animal","termid":"MONDO:1011424"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement component 2 deficiency, domestic guinea pig","secondary_identifiers":["OMIA:001625-10141"],"synonyms":[{"name":"C2 deficiency, domestic guinea pig","type":"exact"}],"termid":"MONDO:1011486","xrefs":{"Monarch":{"xref_id":"1011486"}}}


id: MONDO:0957821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 88","secondary_identifiers":["MEDGEN:1845113","UMLS:C5882706","OMIM:620547","DOID:0070587"],"termid":"MONDO:0957821","xrefs":{"Monarch":{"xref_id":"0957821"}}}


id: FYPO:0004123
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a glutathione disulfide oxidoreductase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257","FYPO:0000654"],"is_obsolete":false,"name":"normal glutathione disulfide oxidoreductase activity","termid":"FYPO:0004123"}


id: GO:1904434
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ferrous iron binding.","definition_xrefs":["GOC:BHF","PMID:18353247","GOC:kom","GOC:TermGenie","GO_REF:0000059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of binding","termid":"GO:0051099"}],"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 ferrous iron binding","synonyms":[{"name":"activation of ferrous iron binding","type":"narrow"},{"name":"up regulation of ferrous iron binding","type":"exact"},{"name":"up-regulation of ferrous iron binding","type":"exact"},{"name":"upregulation of ferrous iron binding","type":"exact"}],"termid":"GO:1904434"}


id: PBO:0057685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1273h","termid":"PBO:0057685"}


id: PBO:0050640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock transcription factor Y-linked 5, pseudogene","termid":"PBO:0050640"}


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: GO:0018764
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-isopropylammelide + H2O = cyanuric acid + isopropylamine.","definition_xrefs":["EC:3.5.4.42"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds","termid":"GO:0016810"}],"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:0016787"},{"rel_name":"is_a","termid":"GO:0016810"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016810"],"is_obsolete":false,"name":"N-isopropylammelide isopropylaminohydrolase activity","secondary_identifiers":["RHEA:23608","MetaCyc:R123-RXN","UM-BBD_enzymeID:r0115"],"synonyms":[{"name":"AtzC","type":"related"}],"termid":"GO:0018764"}


id: MONDO:0023194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete frints de Smet Fabry Fryns syndrome (obsolete MONDO:0023194)","termid":"MONDO:0023194","xrefs":{"Monarch":{"xref_id":"0023194"}}}


id: FYPO:0006782
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 a protein measured in a complex that is a precursor of the large ribosomal subunit is lower than normal.","definition_xrefs":["PomBase:mah","PMID:27667686"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"},{"relation_name":"is_a","term_name":"abnormal protein complex composition","termid":"FYPO:0005003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0006551"],"is_obsolete":false,"name":"decreased protein level in large ribosomal subunit precursor","synonyms":[{"name":"decreased large ribosomal subunit precursor complex protein level during vegetative growth","type":"exact"},{"name":"decreased protein level in large ribosomal subunit precursor during mitotic cell cycle","type":"related"},{"name":"decreased protein level in large ribosomal subunit precursor during vegetative growth","type":"exact"},{"name":"decreased protein level in preribosome, large subunit precursor","type":"exact"},{"name":"reduced protein level in large ribosomal subunit precursor","type":"exact"}],"termid":"FYPO:0006782"}


id: MONDO:0007886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the body of the uterus. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C3434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"fibroma","termid":"MONDO:0005167"},{"relation_name":"is_a","term_name":"benign neoplasm of corpus uteri","termid":"MONDO:0021525"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterine corpus leiomyoma","secondary_identifiers":["ONCOTREE:ULM","SCTID:95315005","UMLS:C0042133","OMIM:150699","ICD9:218","EFO:0000731","ICD9:218.9","MEDGEN:21801","NCIT:C7052","DOID:13223","HP:0000131","MESH:D047708"],"synonyms":[{"name":"UL","type":"related"},{"name":"body of uterus fibroid","type":"exact"},{"name":"body of uterus leiomyoma","type":"exact"},{"name":"corpus uteri fibroid","type":"exact"},{"name":"corpus uteri leiomyoma","type":"exact"},{"name":"fibroid of body of uterus","type":"exact"},{"name":"fibroid of corpus uteri","type":"exact"},{"name":"fibroid of the body of uterus","type":"exact"},{"name":"fibroid of the corpus uteri","type":"exact"},{"name":"fibroid of the uterine body","type":"exact"},{"name":"fibroid of the uterine corpus","type":"exact"},{"name":"fibroid of uterine body","type":"exact"},{"name":"fibroid of uterine corpus","type":"exact"},{"name":"leiomyoma of body of uterus","type":"exact"},{"name":"leiomyoma of corpus uteri","type":"exact"},{"name":"leiomyoma of the body of uterus","type":"exact"},{"name":"leiomyoma of the corpus uteri","type":"exact"},{"name":"leiomyoma of the uterine body","type":"exact"},{"name":"leiomyoma of the uterine corpus","type":"exact"},{"name":"leiomyoma of uterine body","type":"exact"},{"name":"leiomyoma of uterine corpus","type":"exact"},{"name":"leiomyoma, uterine","type":"related"},{"name":"plexiform leiomyoma","type":"exact"},{"name":"uterine body fibroid","type":"exact"},{"name":"uterine body leiomyoma","type":"exact"},{"name":"uterine corpus fibroid","type":"exact"},{"name":"uterine corpus leiomyoma","type":"exact"},{"name":"uterine corpus leiomyomata","type":"exact"},{"name":"uterine fibroid","type":"exact"},{"name":"uterine leiomyoma","type":"related"},{"name":"uterus fibroma","type":"related"}],"termid":"MONDO:0007886","xrefs":{"Monarch":{"xref_id":"0007886"}}}


id: GO:0052110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism reduces the flow of fluid within its host's vascular system, the vessels and tissue that carry or circulate fluids, such as blood, lymph or sap, through the body of an animal or plant. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete occlusion by symbiont of host vascular system (obsolete GO:0052110)","termid":"GO:0052110"}


id: PBO:0040327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit c locus 1 pseudogene 2","termid":"PBO:0040327"}


id: GO:0047982
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-homocysteine + H2O = sulfide + NH3 + 2-oxobutanoate.","definition_xrefs":["MetaCyc:HOMOCYSTEINE-DESULFHYDRASE-RXN","EC:4.4.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"homocysteine desulfhydrase activity","secondary_identifiers":["RHEA:14501","Reactome:R-HSA-1614631"],"synonyms":[{"name":"L-homocysteine hydrogen-sulfide-lyase (deaminating)","type":"related"},{"name":"L-homocysteine hydrogen-sulfide-lyase (deaminating; 2-oxobutanoate-forming)","type":"related"},{"name":"homocysteine desulfurase activity","type":"related"}],"termid":"GO:0047982"}


id: PBO:0063895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol glycan anchor biosynthesis class S","termid":"PBO:0063895"}


id: GO:0070577
data:
  {"annotated_genes":["SJAG_05252","SJAG_02625","SJAG_02500","SJAG_00591","SJAG_02701","SJAG_00837"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70410,75094,76887,78581,78792,79798],"is_not":false,"summary":null,"term":"GO:0070577"}]},"cv_name":"molecular_function","definition":"Binding to a histone in which a lysine residue has been modified by acetylation.","definition_xrefs":["GOC:BHF","GOC:rl","GOC:mah","PMID:17582821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone binding","termid":"GO:0042393"},{"relation_name":"is_a","term_name":"acetylation-dependent protein binding","termid":"GO:0140033"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00591":null,"SJAG_00837":null,"SJAG_02500":null,"SJAG_02625":null,"SJAG_02701":null,"SJAG_05252":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"lysine-acetylated histone binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"acetylated histone residue binding","type":"broad"}],"termid":"GO:0070577","terms_by_termid":{"GO:0070577":null}}


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


id: PBO:0111341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SHREC complex subunit Clr2","termid":"PBO:0111341"}


id: MONDO:0007160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Stickler syndrome","termid":"MONDO:0019354"},{"relation_name":"is_a","term_name":"type 2 collagenopathy","termid":"MONDO:0022800"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0005328","MONDO:0005559"],"is_obsolete":false,"name":"Stickler syndrome type 1","secondary_identifiers":["UMLS:C2020284","DOID:0080676","GARD:5018","MESH:C537492","NANDO:2201354","NCIT:C168733","Orphanet:90653","icd11.foundation:203625278","OMIM:108300","MEDGEN:810955"],"synonyms":[{"name":"STL1","type":"related"},{"name":"Stickler syndrome type 1","type":"exact"},{"name":"Stickler syndrome, membranous vitreous type","type":"related"},{"name":"Stickler syndrome, type 1","type":"related"},{"name":"Stickler syndrome, type I","type":"related"},{"name":"Stickler syndrome, vitreous type 1","type":"related"},{"name":"arthroophthalmopathy, hereditary progressive","type":"related"}],"termid":"MONDO:0007160","xrefs":{"Monarch":{"xref_id":"0007160"}}}


id: PBO:0078605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 60 pseudogene 18","termid":"PBO:0078605"}


id: PBO:0045399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPPA3 pseudogene 1","termid":"PBO:0045399"}


id: GO:0002025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that results in an increase in the diameter of an artery during the norepinephrine-epinephrine response to blood pressure change.","definition_xrefs":["PMID:10358008","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of systemic arterial blood pressure","termid":"GO:0003085"},{"relation_name":"is_a","term_name":"vasodilation","termid":"GO:0042311"},{"relation_name":"part_of","term_name":"regulation of systemic arterial blood pressure by norepinephrine-epinephrine","termid":"GO:0001993"}],"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":"norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure","synonyms":[{"name":"noradrenaline-adrenaline vasodilation involved in regulation of blood pressure","type":"exact"},{"name":"norepinephrine-epinephrine vasodilation during blood pressure regulation","type":"exact"},{"name":"vasodilation by norepinephrine-epinephrine involved in regulation of systemic arterial blood pressure","type":"exact"}],"termid":"GO:0002025"}


id: PBO:0063144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate and testis expressed 4","termid":"PBO:0063144"}


id: PBO:0002186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-end-recognizing protein (predicted)","termid":"PBO:0002186"}


id: FYPO:0003503
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell has a normal length.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell size","termid":"FYPO:0001124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal vegetative cell length","synonyms":[{"name":"normal cell length during vegetative growth","type":"exact"},{"name":"normal vegetative cell length during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003503"}


id: GO:2000333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of blood microparticle formation.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"is_a","term_name":"regulation of blood microparticle formation","termid":"GO:2000332"},{"relation_name":"negatively_regulates","term_name":"blood microparticle formation","termid":"GO:0072564"}],"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 blood microparticle formation","synonyms":[{"name":"negative regulation of microparticle generation","type":"exact"},{"name":"negative regulation of microparticle release","type":"exact"}],"termid":"GO:2000333"}


id: PBO:0028378
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_xanthine_DNA_N-glycosylase_activity","termid":"PBO:0028378"}


id: GO:0102546
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2R)-2-O-(alpha-D-mannosyl)-glycerate + H2O = (R)-glycerate + D-mannose.","definition_xrefs":["RHEA:58456"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ether hydrolase activity","termid":"GO:0016803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"mannosylglycerate hydrolase activity","secondary_identifiers":["EC:3.2.1.170","MetaCyc:RXN-14900"],"termid":"GO:0102546"}


id: PBO:0065686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pituitary tumor-transforming 2","termid":"PBO:0065686"}


id: PBO:0051329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2-23 (pseudogene)","termid":"PBO:0051329"}


id: PBO:0089976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snoRNP assembly factor Naf1","termid":"PBO:0089976"}


id: PBO:0071463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 4","termid":"PBO:0071463"}


id: PBO:0117053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYO7B antisense RNA 1","termid":"PBO:0117053"}


id: MOD:00168
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-aspartic acid residue to N-(aspart-1-yl)-glycosylphosphatidylinositolethanolamine.","definition_xrefs":["PubMed:7120400","RESID:AA0159"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosylphosphatidylinositolated residue","termid":"MOD:00818"},{"relation_name":"is_a","term_name":"modified L-aspartic acid residue","termid":"MOD:00904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"},{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:01155","MOD:00764"],"is_obsolete":false,"name":"N-aspartyl-glycosylphosphatidylinositolethanolamine","synonyms":[{"name":"GPIAsp","type":"exact"},{"name":"LIPID GPI-anchor amidated aspartate","type":"exact"},{"name":"N-aspartyl-glycosylphosphatidylinositolethanolamine","type":"exact"}],"termid":"MOD:00168"}


id: GO:0016515
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-13 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:jl","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"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:0038023","GO:0003674"],"is_obsolete":false,"name":"interleukin-13 receptor activity","synonyms":[{"name":"IL-13 receptor activity","type":"exact"},{"name":"IL-13R","type":"exact"}],"termid":"GO:0016515"}


id: GO:0070320
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents, or reduces the activity of an inwardly rectifying potassium channel.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium channel inhibitor activity","termid":"GO:0019870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0098772","GO:0140678","GO:0003674"],"is_obsolete":false,"name":"inward rectifier potassium channel inhibitor activity","termid":"GO:0070320"}


id: PBO:0078339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (CTC) 5-1","termid":"PBO:0078339"}


id: PBO:0070293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, variant U1 small nuclear 34","termid":"PBO:0070293"}


id: PBO:0075515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPCS3 antisense RNA 1","termid":"PBO:0075515"}


id: PBO:0070170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 84 pseudogene","termid":"PBO:0070170"}


id: PBO:0068524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 123, pseudogene","termid":"PBO:0068524"}


id: MONDO:0004439
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the periocular region.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"periocular meningioma","secondary_identifiers":["UMLS:C1335383","DOID:8030","MEDGEN:233849","NCIT:C6777"],"termid":"MONDO:0004439","xrefs":{"Monarch":{"xref_id":"0004439"}}}


id: MONDO:0002850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm with skeletal muscle differentiation affecting the central nervous system.","definition_xrefs":["NCIT:C5464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system sarcoma","termid":"MONDO:0002217"},{"relation_name":"is_a","term_name":"rhabdomyosarcoma","termid":"MONDO:0005212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"central nervous system rhabdomyosarcoma","secondary_identifiers":["MEDGEN:232043","UMLS:C1332891","DOID:4048"],"synonyms":[{"name":"CNS rhabdomyosarcoma","type":"exact"},{"name":"central nervous system rhabdomyosarcoma","type":"exact"},{"name":"central nervous system rhabdomyosarcoma (disease)","type":"exact"},{"name":"rhabdomyosarcoma (disease) of central nervous system","type":"exact"},{"name":"rhabdomyosarcoma of CNS","type":"exact"},{"name":"rhabdomyosarcoma of central nervous system","type":"exact"},{"name":"rhabdomyosarcoma of the CNS","type":"exact"},{"name":"rhabdomyosarcoma of the central nervous system","type":"exact"}],"termid":"MONDO:0002850","xrefs":{"Monarch":{"xref_id":"0002850"}}}


id: FYPO:0000692
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of DNA-1,N6-ethenoadenine N-glycosylase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA N-glycosylase activity","termid":"FYPO:0008216"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000652","FYPO:0000661","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"abnormal DNA-1,N6-ethenoadenine N-glycosylase activity","termid":"FYPO:0000692"}


id: PBO:0080226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"viral integration site 1","termid":"PBO:0080226"}


id: PBO:0045882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 delta pseudogene 6","termid":"PBO:0045882"}


id: GO:0005200
data:
  {"annotated_genes":["SJAG_04387","SJAG_01384","SJAG_04003","SJAG_02509","SJAG_03145"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57978,60815,62979,77639,108821],"is_not":false,"summary":null,"term":"GO:0005200"}]},"cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of a cytoskeletal structure.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural molecule activity","termid":"GO:0005198"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01384":null,"SJAG_02509":null,"SJAG_03145":null,"SJAG_04003":null,"SJAG_04387":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005198"}],"interesting_parent_ids":["GO:0005198","GO:0003674"],"is_obsolete":false,"name":"structural constituent of cytoskeleton","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0005200","terms_by_termid":{"GO:0005200":null}}


id: MONDO:1012947
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited bone disorder that occurs in chickens and is characterized by abnormal limb development.","definition_xrefs":["PMID:10912683"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ametapodia, chicken","termid":"MONDO:1012947","xrefs":{"Monarch":{"xref_id":"1012947"}}}


id: MONDO:0003239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Camurati-Engelmann disease (obsolete MONDO:0003239)","termid":"MONDO:0003239","xrefs":{"Monarch":{"xref_id":"0003239"}}}


id: GO:0035185
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The first nine mitotic division cycles of the insect embryo, during which the dividing nuclei lie deep in the interior of the egg and divide nearly synchronously. This is the first phase of the syncytial period where nuclei divide in a common cytoplasm without cytokinesis.","definition_xrefs":["ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle comprising mitosis without cytokinesis","termid":"GO:0033301"},{"relation_name":"is_a","term_name":"mitotic cell cycle, embryonic","termid":"GO:0045448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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":"preblastoderm mitotic cell cycle","termid":"GO:0035185"}


id: PATO:0002390
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A length quality which is equal to the length of any straight line segment that passes from the center of a circle to any endpoint on the circular boundary. The radius is half of the diameter.","definition_xrefs":["PATO:DS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"length","termid":"PATO:0000122"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"radius","termid":"PATO:0002390"}


id: PBO:0036404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anamorsin family iron-sulfur cluster protein Dre2 (predicted)","termid":"PBO:0036404"}


id: GO:1902707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of hexose to ethanol.","definition_xrefs":["GO_REF:0000093","GOC:mengo_curators","GOC:TermGenie","PMID:19539744","PMID:18727018"],"gene_count":0,"genotype_count":0,"name":"obsolete hexose catabolic process to ethanol (obsolete GO:1902707)","synonyms":[{"name":"hexose breakdown to ethanol","type":"exact"},{"name":"hexose catabolism to ethanol","type":"exact"},{"name":"hexose degradation to ethanol","type":"exact"},{"name":"solventogenesis","type":"broad"}],"termid":"GO:1902707"}


id: GO:0035388
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the Roundabout signaling pathway.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of Roundabout signaling pathway","termid":"GO:0035386"},{"relation_name":"positively_regulates","term_name":"Roundabout signaling pathway","termid":"GO:0035385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of Roundabout signaling pathway","synonyms":[{"name":"positive regulation of Roundabout signalling pathway","type":"exact"}],"termid":"GO:0035388"}


id: GO:0004032
data:
  {"annotated_genes":["SJAG_04660","SJAG_02010","SJAG_03958","SJAG_01869"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74038,91576],"is_not":false,"summary":null,"term":"GO:0004032"},{"annotations":[100940,95510],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032866"},{"annotations":[95511,100941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032867"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: an alditol + NADP+ = an aldose + NADPH + H+.","definition_xrefs":["EC:1.1.1.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol dehydrogenase (NADP+) activity","termid":"GO:0008106"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01869":null,"SJAG_02010":null,"SJAG_03958":null,"SJAG_04660":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"aldose reductase (NADPH) activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-196060","KEGG_REACTION:R02820","Reactome:R-HSA-5652172","RHEA:12789"],"synonyms":[{"name":"aldehyde reductase activity","type":"related"},{"name":"alditol:NADP+ 1-oxidoreductase activity","type":"exact"},{"name":"aldose reductase activity","type":"related"},{"name":"polyol dehydrogenase (NADP(+)) activity","type":"related"}],"termid":"GO:0004032","terms_by_termid":{"GO:0004032":null,"GO:0032866":null,"GO:0032867":null}}


id: MONDO:0030934
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intellectual disability, autosomal dominant","termid":"MONDO:0100172"}],"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":"intellectual developmental disorder, autosomal dominant 64","secondary_identifiers":["OMIM:619188","UMLS:C5543067","GARD:16478","MEDGEN:1784554"],"synonyms":[{"name":"MRD64","type":"exact"},{"name":"intellectual developmental disorder, autosomal dominant 64","type":"exact"},{"name":"mental retardation, autosomal dominant 64","type":"exact"}],"termid":"MONDO:0030934","xrefs":{"Monarch":{"xref_id":"0030934"}}}


id: GO:0102866
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an (8Z,11Z,14Z)-icosatrienoyl-containing glycerolipid + 2 Fe(II)-[cytochrome b5] + 2 H+ + O2 = (5Z,8Z,11Z,14Z)-eicosatetraenoyl-containing glycerolipid + 2 Fe(III)-[cytochrome b5] + 2 H2O. Also converts an (8Z,11Z,14Z,17Z)-eicosatetraenoyl-containing glycerolipid into a (5Z,8Z,11Z,14Z,17Z)-eicosapentaenoyl-containing glycerolipid.","definition_xrefs":["EC:1.14.19.30"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water","termid":"GO:0016717"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"acyl-lipid (8-3)-desaturase activity","synonyms":[{"name":"Delta(5)-fatty-acid desaturase activity","type":"exact"},{"name":"acyl-lipid 5-desaturase activity","type":"related"},{"name":"di-homo-gamma-linolenate delta5 desaturase activity","type":"related"}],"termid":"GO:0102866"}


id: MONDO:0000634
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm arising from any of the organs of the thoracic cavity. Representative examples include pleural adenomatoid tumor, chest wall lipoma, mediastinal schwannoma, and lung hamartoma.","definition_xrefs":["NCIT:C4565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm","termid":"MONDO:0005165"},{"relation_name":"is_a","term_name":"neoplasm of thorax","termid":"MONDO:0021350"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thoracic benign neoplasm","secondary_identifiers":["MONDO:0021448","ICD9:229.8","MEDGEN:138065","UMLS:C0346440","DOID:0060097","SCTID:255059002"],"synonyms":[{"name":"benign neoplasm of the thorax","type":"exact"},{"name":"benign neoplasm of thorax","type":"exact"},{"name":"benign thoracic neoplasm","type":"exact"},{"name":"benign thoracic tumor","type":"exact"},{"name":"benign thoracic tumour","type":"exact"},{"name":"benign tumor of the thorax","type":"exact"},{"name":"benign tumor of thorax","type":"exact"},{"name":"benign tumour of the thorax","type":"exact"},{"name":"benign tumour of thorax","type":"exact"},{"name":"thoracic segment of trunk benign neoplasm","type":"exact"}],"termid":"MONDO:0000634","xrefs":{"Monarch":{"xref_id":"0000634"}}}


id: MOD:01640
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes or replaces an L-isoleucine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-isoleucine residue","termid":"MOD:00910"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue removal","termid":"MOD:01651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-isoleucine removal","termid":"MOD:01640"}


id: PBO:0062925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purinergic receptor P2Y12","termid":"PBO:0062925"}


id: GO:0047878
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + erythritol = D-erythritol 4-phosphate + ADP + 2 H+.","definition_xrefs":["EC:2.7.1.27","RHEA:20708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"erythritol kinase activity","secondary_identifiers":["MetaCyc:ERYTHRITOL-KINASE-RXN","KEGG_REACTION:R02430"],"synonyms":[{"name":"ATP:erythritol 4-phosphotransferase activity","type":"related"},{"name":"erythritol kinase (phosphorylating)","type":"related"}],"termid":"GO:0047878"}


id: GO:0009112
data:
  {"annotated_genes":["SJAG_00392","SJAG_00197","SJAG_01814","SJAG_01673","SJAG_03708","SJAG_01859","SJAG_00694","SJAG_00444","SJAG_04300","SJAG_02593","SJAG_01070","SJAG_05024","SJAG_04297","SJAG_03164","SJAG_02364","SJAG_04709","SJAG_01661","SJAG_00779","SJAG_01997","SJAG_01081","SJAG_06634","SJAG_04299","SJAG_00964","SJAG_03140","SJAG_05287","SJAG_04354"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71719,73762,57647,73172,87548,69796,71425,69505],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006207"},{"annotations":[117098,70444,110114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046084"},{"annotations":[97562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046083"},{"annotations":[73707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006168"},{"annotations":[67872],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006147"},{"annotations":[75236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046100"},{"annotations":[59951,114250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009113"},{"annotations":[91539,73313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006145"},{"annotations":[69665,75102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006144"},{"annotations":[74199,88955,114658,87226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006206"},{"annotations":[91735],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006223"},{"annotations":[117102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009115"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving a nucleobase, a nitrogenous base that is a constituent of a nucleic acid, e.g. the purines: adenine, guanine, hypoxanthine, xanthine and the pyrimidines: cytosine, uracil, thymine.","definition_xrefs":["GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleobase-containing small molecule metabolic process","termid":"GO:0055086"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00392":null,"SJAG_00444":null,"SJAG_00694":null,"SJAG_00779":null,"SJAG_00964":null,"SJAG_01070":null,"SJAG_01081":null,"SJAG_01661":null,"SJAG_01673":null,"SJAG_01814":null,"SJAG_01859":null,"SJAG_01997":null,"SJAG_02364":null,"SJAG_02593":null,"SJAG_03140":null,"SJAG_03164":null,"SJAG_03708":null,"SJAG_04297":null,"SJAG_04299":null,"SJAG_04300":null,"SJAG_04354":null,"SJAG_04709":null,"SJAG_05024":null,"SJAG_05287":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"nucleobase metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"nucleobase metabolism","type":"exact"}],"termid":"GO:0009112","terms_by_termid":{"GO:0006144":null,"GO:0006145":null,"GO:0006147":null,"GO:0006168":null,"GO:0006206":null,"GO:0006207":null,"GO:0006223":null,"GO:0009113":null,"GO:0009115":null,"GO:0046083":null,"GO:0046084":null,"GO:0046100":null}}


id: MONDO:0012407
data:
  {"annotated_genes":["SJAG_01881"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85270],"is_not":false,"summary":null,"term":"MONDO:0012407"}]},"cv_name":"mondo","definition":"A very rare neonatal epileptic encephalopathy disorder characterized clinically by onset of severe seizures within hours of birth that are not responsive to anticonvulsants, but are responsive to treatment with pyridoxal phosphate.","definition_xrefs":["Orphanet:79096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of pyridoxine metabolism","termid":"MONDO:0019237"},{"relation_name":"is_a","term_name":"metabolic epilepsy","termid":"MONDO:0100033"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01881":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0005066"],"is_obsolete":false,"name":"pyridoxal phosphate-responsive seizures","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:604024463","MESH:C566449","OMIM:610090","GARD:10730","DOID:0111329","icd11.foundation:1632334328","MEDGEN:350498","UMLS:C1864723","SCTID:724576005"],"synonyms":[{"name":"PNPO deficiency","type":"exact"},{"name":"PNPO-related neonatal epileptic encephalopathy","type":"exact"},{"name":"PNPOD","type":"related"},{"name":"Pnpo deficiency","type":"related"},{"name":"epileptic encephalopathy, neonatal, Pnpo-related","type":"related"},{"name":"pyridox(am)ine 5’-phosphate oxidase deficiency","type":"exact"},{"name":"pyridoxal 5'-phosphate-dependent epilepsy","type":"related"},{"name":"pyridoxal phosphate-dependent seizures","type":"exact"},{"name":"pyridoxamine 5'-oxidase deficiency","type":"exact"},{"name":"pyridoxamine 5'-phosphate oxidase deficiency","type":"exact"},{"name":"pyridoxamine 5-prime-phosphate oxidase deficiency","type":"related"},{"name":"pyridoxine 5' phosphate oxidase deficiency","type":"exact"},{"name":"pyridoxine-5'-phosphate oxidase deficiency","type":"related"},{"name":"seizures, pyridoxine-resistant, PLP-sensitive","type":"related"}],"termid":"MONDO:0012407","terms_by_termid":{"MONDO:0012407":null},"xrefs":{"Monarch":{"xref_id":"0012407"}}}


id: GO:0032703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of interleukin-2 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-2 production","termid":"GO:0032663"},{"relation_name":"negatively_regulates","term_name":"interleukin-2 production","termid":"GO:0032623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of interleukin-2 production","secondary_identifiers":["GO:0045085","GO:1900041"],"synonyms":[{"name":"down regulation of interleukin-2 production","type":"exact"},{"name":"down-regulation of interleukin-2 production","type":"exact"},{"name":"downregulation of interleukin-2 production","type":"exact"},{"name":"inhibition of interleukin-2 production","type":"narrow"},{"name":"negative regulation of IL-2 production","type":"exact"},{"name":"negative regulation of interleukin-2 biosynthetic process","type":"narrow"},{"name":"negative regulation of interleukin-2 secretion","type":"narrow"}],"termid":"GO:0032703"}


id: PBO:0058617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6749","termid":"PBO:0058617"}


id: SO:0000661
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000661 intron_attribute (obsolete SO:0000661)","termid":"SO:0000661"}


id: PBO:0089208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfite reductase NADPH flavoprotein subunit","termid":"PBO:0089208"}


id: MONDO:0008451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominant neurodegenerative disorder characterized by juvenile onset, distal motor weakness without sensory impairment, and anterior horn cell degeneration.","definition_xrefs":["NCIT:C132826"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuronopathy, distal hereditary motor (obsolete MONDO:0000075)","termid":"MONDO:0000075"},{"relation_name":"is_a","term_name":"neuronopathy, distal hereditary motor, autosomal dominant","termid":"MONDO:0015362"},{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559","MONDO:0005244"],"is_obsolete":false,"name":"neuronopathy, distal hereditary motor, autosomal dominant 1","secondary_identifiers":["OMIM:182960","DOID:0111200","UMLS:C1866784","MEDGEN:356618","GARD:16953","MESH:C566675","Orphanet:139518"],"synonyms":[{"name":"Charcot-Marie-Tooth disease, spinal, 1","type":"related"},{"name":"Charcot-Marie-Tooth disease, spinal, I","type":"exact"},{"name":"DHMN1","type":"exact"},{"name":"HMN 1","type":"related"},{"name":"HMN1","type":"related"},{"name":"autosomal dominant distal juvenile spinal muscular atrophy type 1","type":"exact"},{"name":"dHMN1","type":"exact"},{"name":"distal hereditary motor neuronopathy type I","type":"exact"},{"name":"neuronopathy, distal hereditary motor, type 1","type":"exact"},{"name":"neuronopathy, distal hereditary motor, type I","type":"related"},{"name":"neuropathy, distal hereditary motor, type 1","type":"related"},{"name":"spinal muscular atrophy, distal, juvenile, autosomal dominant, 1","type":"related"}],"termid":"MONDO:0008451","xrefs":{"Monarch":{"xref_id":"0008451"}}}


id: GO:0047323
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + L-seryl-[3-methyl-2-oxobutanoate dehydrogenase] = ADP + H+ + O-phospho-L-seryl-[3-methyl-2-oxobutanoate dehydrogenase].","definition_xrefs":["RHEA:17301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004672"}],"interesting_parent_ids":["GO:0004672","GO:0003674","GO:0003824","GO:0016301","GO:0016740","GO:0140096"],"is_obsolete":false,"name":"[3-methyl-2-oxobutanoate dehydrogenase (acetyl-transferring)] kinase activity","secondary_identifiers":["Reactome:R-HSA-9912480","MetaCyc:2.7.11.4-RXN","EC:2.7.11.4","Reactome:R-HSA-5693148"],"synonyms":[{"name":"3-methyl-2-oxobutanoate dehydrogenase (acetyl-transferring) kinase activity","type":"related"},{"name":"ATP:3-methyl-2-oxobutanoate dehydrogenase (acetyl-transferring) phosphotransferase activity","type":"related"},{"name":"BCK","type":"related"},{"name":"BCKD kinase activity","type":"related"},{"name":"BCODH kinase activity","type":"related"},{"name":"STK2","type":"related"},{"name":"[3-methyl-2-oxobutanoate dehydrogenase (lipoamide)] kinase activity","type":"exact"},{"name":"branched-chain 2-oxo acid dehydrogenase kinase activity","type":"related"},{"name":"branched-chain alpha-ketoacid dehydrogenase kinase activity","type":"related"},{"name":"branched-chain keto acid dehydrogenase kinase activity","type":"related"},{"name":"branched-chain oxo acid dehydrogenase kinase (phosphorylating) activity","type":"related"}],"termid":"GO:0047323"}


id: MONDO:0005167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm arising from the fibrous tissue. It is characterized by the presence of spindle-shaped fibroblasts.","definition_xrefs":["NCIT:C3041"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroblastic neoplasm","termid":"MONDO:0006209"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroma","secondary_identifiers":["ICD9:215.9","EFO:0002424","MEDGEN:42016","MESH:D005350","ICDO:8810/0","SCTID:424568000","UMLS:C0016045","DOID:0050871"],"synonyms":[{"name":"fibroma","type":"exact"},{"name":"fibroma, benign","type":"exact"}],"termid":"MONDO:0005167","xrefs":{"Monarch":{"xref_id":"0005167"}}}


id: GO:0008586
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which anatomical structures of the veins on an imaginal disc-derived wing are generated and organized.","definition_xrefs":["GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"imaginal disc-derived wing morphogenesis","termid":"GO:0007476"}],"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":"imaginal disc-derived wing vein morphogenesis","synonyms":[{"name":"wing vein morphogenesis","type":"exact"}],"termid":"GO:0008586"}


id: PBO:0058498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5692a-1","termid":"PBO:0058498"}


id: PBO:0001788
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"predominantly uniformly single copy (one ot one)","termid":"PBO:0001788"}


id: PBO:0046755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EXOC7 pseudogene 1","termid":"PBO:0046755"}


id: GO:0021637
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the oculomotor nerve. This process pertains to the physical shaping of a rudimentary structure. The trigeminal nerve is composed of three large branches. They are the ophthalmic (V1, sensory), maxillary (V2, sensory) and mandibular (V3, motor and sensory) branches. The sensory ophthalmic branch travels through the superior orbital fissure and passes through the orbit to reach the skin of the forehead and top of the head. The maxillary nerve contains sensory branches that reach the pterygopalatine fossa via the inferior orbital fissure (face, cheek and upper teeth) and pterygopalatine canal (soft and hard palate, nasal cavity and pharynx). The motor part of the mandibular branch is distributed to the muscles of mastication, the mylohyoid muscle and the anterior belly of the digastric. The mandibular nerve also innervates the tensor veli palatini and tensor tympani muscles. The sensory part of the mandibular nerve is composed of branches that carry general sensory information from the mucous membranes of the mouth and cheek, anterior two-thirds of the tongue, lower teeth, skin of the lower jaw, side of the head and scalp and meninges of the anterior and middle cranial fossae.","definition_xrefs":["GOC:jid","GOC:cls","ISBN:0838580343","GO_REF:0000021","GOC:dph","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve structural organization","termid":"GO:0021604"},{"relation_name":"part_of","term_name":"trigeminal nerve morphogenesis","termid":"GO:0021636"}],"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":"trigeminal nerve structural organization","synonyms":[{"name":"CN V structural organization","type":"related"},{"name":"trigeminal nerve structural organisation","type":"exact"}],"termid":"GO:0021637"}


id: GO:0002935
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: adenosine37 in tRNA + 2 reduced [2Fe-2S]-[ferredoxin] + 2 S-adenosyl-L-methionine = 2-methyladenosine37 in tRNA + 5'-deoxyadenosine + L-methionine + 2 oxidized [2Fe-2S]-[ferredoxin] + S-adenosyl-L-homocysteine.","definition_xrefs":["RHEA:43332","PMID:22891362"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-methyltransferase activity","termid":"GO:0008169"},{"relation_name":"is_a","term_name":"tRNA (adenine) methyltransferase activity","termid":"GO:0016426"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0140098","GO:0140101","GO:0016741","GO:0016740"],"is_obsolete":false,"name":"tRNA (adenine(37)-C2)-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN0-7007"],"synonyms":[{"name":"tRNA (adenine(37)-C(2))-methyltransferase activity","type":"exact"},{"name":"tRNA (adenosine(37)-C2-)-methyltransferase activity","type":"exact"}],"termid":"GO:0002935"}


id: GO:0005119
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a smoothened (smo) protein, which interacts with patched to transmit hedgehog signals.","definition_xrefs":["GOC:ceb","PMID:11731473"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"smoothened binding","synonyms":[{"name":"smo binding","type":"exact"},{"name":"smo ligand","type":"narrow"},{"name":"smoothened ligand","type":"narrow"}],"termid":"GO:0005119"}


id: GO:0070826
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cytoplasmic protein complex that contains integrin, mobilferrin and a flavin monooxygenase, is capable of reducing Fe(III) to Fe(II) utilizing NADPH, and is involved in iron transport. Fe(II) is required in the cell as the substrate for ferrochelatase in the synthesis of heme.","definition_xrefs":["GOC:mah","GOC:rph","PMID:11842004","PMID:8639593"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"paraferritin complex","termid":"GO:0070826"}


id: GO:1904873
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of telomerase RNA localization to Cajal body.","definition_xrefs":["GOC:nc","GOC:TermGenie","GOC:BHF","PMID:25467444","GO_REF:0000058","GOC:BHF_telomere"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biological process","termid":"GO:0048519"},{"relation_name":"is_a","term_name":"regulation of telomerase RNA localization to Cajal body","termid":"GO:1904872"},{"relation_name":"negatively_regulates","term_name":"telomerase RNA localization to Cajal body","termid":"GO:0090671"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of telomerase RNA localization to Cajal body","synonyms":[{"name":"down regulation of telomerase RNA localization to Cajal body","type":"exact"},{"name":"down-regulation of telomerase RNA localization to Cajal body","type":"exact"},{"name":"downregulation of telomerase RNA localization to Cajal body","type":"exact"},{"name":"inhibition of telomerase RNA localization to Cajal body","type":"narrow"}],"termid":"GO:1904873"}


id: MONDO:0015080
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete thymic tumor (obsolete MONDO:0015080)","termid":"MONDO:0015080","xrefs":{"Monarch":{"xref_id":"0015080"}}}


id: MONDO:0016407
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oligomeganephronia is a developmental anomaly of the kidneys, and the most severe form of renal hypoplasia, characterized by a reduction of 80% in nephron number and a marked hypertrophy of the glomeruli and tubules.","definition_xrefs":["Orphanet:2260"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"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":"oligomeganephronia","secondary_identifiers":["icd11.foundation:1283447040","MEDGEN:609100","NANDO:2200159","GARD:4066","SCTID:18417009","UMLS:C0431694","NCIT:C123202","DOID:0111142","ICD10CM:Q60.4"],"synonyms":[{"name":"Oligomeganephronic renal hypoplasia","type":"exact"}],"termid":"MONDO:0016407","xrefs":{"Monarch":{"xref_id":"0016407"}}}


id: GO:0051182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a coenzyme into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. A coenzyme is any of various nonprotein organic cofactors that are required, in addition to an enzyme and a substrate, for an enzymatic reaction to proceed.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete coenzyme transport (obsolete GO:0051182)","termid":"GO:0051182"}


id: PBO:0041587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbonic anhydrase 2","termid":"PBO:0041587"}


id: PBO:0063762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHC2 antisense RNA 1","termid":"PBO:0063762"}


id: PBO:0090911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane NiCoT heavy metal ion transmembrane transporter Nic1","termid":"PBO:0090911"}


id: PBO:0064213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase B domain containing 2","termid":"PBO:0064213"}


id: PBO:0031041
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_concentration_of_DHA_in_growth_medium","termid":"PBO:0031041"}


id: PBO:0059418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S36 pseudogene 4","termid":"PBO:0059418"}


id: GO:0060282
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate or extent of the process whose specific outcome is the progression of an oocyte over time, from initial commitment of the cell to its specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell development","termid":"GO:0010720"},{"relation_name":"is_a","term_name":"regulation of oocyte development","termid":"GO:0060281"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"oocyte development","termid":"GO:0048599"}],"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 oocyte development","termid":"GO:0060282"}


id: PBO:0028320
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_nucleus_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0028320"}


id: PATO:0001334
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A length quality which is equal to the length of any straight line segment that passes through the center of a circle and whose endpoints are on the circular boundary.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Diameter"],"direct_ancestors":[{"relation_name":"is_a","term_name":"length","termid":"PATO:0000122"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diameter","termid":"PATO:0001334"}


id: GO:0018846
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: styrene oxide = phenylacetaldehyde.","definition_xrefs":["EC:5.3.99.7","RHEA:21604"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity","termid":"GO:0016860"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"styrene-oxide isomerase activity","secondary_identifiers":["KEGG_REACTION:R02615","MetaCyc:STYRENE-OXIDE-ISOMERASE-RXN","UM-BBD_reactionID:r0034"],"synonyms":[{"name":"SOI activity","type":"related"},{"name":"styrene oxide isomerase activity","type":"exact"},{"name":"styrene-oxide isomerase (epoxide-cleaving)","type":"related"}],"termid":"GO:0018846"}


id: PBO:0089607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial serine/threonine protein phosphatase PP2C catalytic subunit Ptc4","termid":"PBO:0089607"}


id: PBO:0059233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L3 pseudogene 1","termid":"PBO:0059233"}


id: MONDO:0012257
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic renal or urinary tract malformation (obsolete MONDO:0019721)","termid":"MONDO:0019721"},{"relation_name":"excluded_subClassOf","term_name":"familial cystic renal disease","termid":"MONDO:0019741"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cerebrorenodigital syndrome","secondary_identifiers":["OMIM:609345","GARD:15458","MESH:C563731","Orphanet:1396","MEDGEN:373053","UMLS:C1836287"],"synonyms":[{"name":"CEREBRORENODIGITAL syndrome with limb malformations and triradiate acetabula","type":"related"}],"termid":"MONDO:0012257","xrefs":{"Monarch":{"xref_id":"0012257"}}}


id: GO:0106277
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: bilirubin IXalpha + NADP+ = biliverdin IXalpha + NADPH + H+.","definition_xrefs":["RHEA:15793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biliverdin reductase [NAD(P)+] activity","termid":"GO:0004074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"biliverdin reductase (NADP+) activity","termid":"GO:0106277"}


id: MONDO:0009098
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":"dextrocardia with unusual facies and microphthalmia","secondary_identifiers":["UMLS:C1857298","MEDGEN:346559","MESH:C538269","OMIM:221950"],"synonyms":[{"name":"Aughton syndrome","type":"related"},{"name":"dextrocardia with unusual facies and microphthalmia","type":"exact"},{"name":"dextrocardia, microphthalmia, cleft palate, choreoathetosis and intellectual disability","type":"related"},{"name":"dextrocardia, microphthalmia, cleft palate, choreoathetosis and mental retardation","type":"related"}],"termid":"MONDO:0009098","xrefs":{"Monarch":{"xref_id":"0009098"}}}


id: GO:1900445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of filamentous growth of a population of unicellular organisms in response to biotic stimulus.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to biotic stimulus","termid":"GO:0002833"},{"relation_name":"is_a","term_name":"positive regulation of filamentous growth of a population of unicellular organisms","termid":"GO:1900430"},{"relation_name":"is_a","term_name":"regulation of filamentous growth of a population of unicellular organisms in response to biotic stimulus","termid":"GO:1900443"},{"relation_name":"positively_regulates","term_name":"filamentous growth of a population of unicellular organisms in response to biotic stimulus","termid":"GO:0036180"}],"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 filamentous growth of a population of unicellular organisms in response to biotic stimulus","synonyms":[{"name":"activation of filamentous growth of a population of unicellular organisms in response to biotic stimulus","type":"narrow"},{"name":"up regulation of filamentous growth of a population of unicellular organisms in response to biotic stimulus","type":"exact"},{"name":"up-regulation of filamentous growth of a population of unicellular organisms in response to biotic stimulus","type":"exact"},{"name":"upregulation of filamentous growth of a population of unicellular organisms in response to biotic stimulus","type":"exact"}],"termid":"GO:1900445"}


id: GO:0032562
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to dAMP, deoxyadenosine monophosphate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenyl deoxyribonucleotide binding","termid":"GO:0032558"},{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"dAMP binding","termid":"GO:0032562"}


id: GO:0001164
data:
  {"annotated_genes":["SJAG_00692","SJAG_02813"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75384,78995],"is_not":false,"summary":null,"term":"GO:0001164"}]},"cv_name":"molecular_function","definition":"Binding to a regulatory region composed of the transcription start site and binding sites for transcription factors of the RNA polymerase I transcription machinery. This site is often referred to as the CORE element. In mammalian cells, the CORE element functions in conjunction with the Upstream Control Element (UCE), while in fungi, protozoa, and plants, the CORE element functions without a UCE.","definition_xrefs":["GOC:txnOH","PMID:14969726","PMID:12865296","PMID:8057832"],"direct_ancestors":[{"relation_name":"is_a","term_name":"core promoter sequence-specific DNA binding","termid":"GO:0001046"},{"relation_name":"is_a","term_name":"RNA polymerase I transcription regulatory region sequence-specific DNA binding","termid":"GO:0001163"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00692":null,"SJAG_02813":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0000976"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003677","GO:0000976","GO:0005488"],"is_obsolete":false,"name":"RNA polymerase I core promoter sequence-specific DNA binding","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0001187"],"synonyms":[{"name":"RNA polymerase I CORE element sequence-specific DNA binding","type":"exact"},{"name":"RNA polymerase I CORE element sequence-specific DNA binding transcription factor recruiting transcription factor activity","type":"related"},{"name":"transcription factor activity, RNA polymerase I CORE element binding transcription factor recruiting","type":"related"}],"termid":"GO:0001164","terms_by_termid":{"GO:0001164":null}}


id: PBO:0111352
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 Utp13","termid":"PBO:0111352"}


id: GO:0050071
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,2-diacyl-sn-glycero-3-phospho-(1'-sn-glycerol) + L-lysyl-tRNA(Lys) = 1,2-diacyl-sn-glycero-3-phospho-1'-(3'-O-L-lysyl)-sn-glycerol + tRNA(Lys).","definition_xrefs":["EC:2.3.2.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyltransferase activity","termid":"GO:0016755"}],"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:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016746","GO:0016740"],"is_obsolete":false,"name":"phosphatidylglycerol lysyltransferase activity","secondary_identifiers":["RHEA:10668","MetaCyc:LYSYLTRANSFERASE-RXN"],"synonyms":[{"name":"lysylphosphatidylglycerol synthase activity","type":"exact"},{"name":"lysyltransferase activity","type":"broad"}],"termid":"GO:0050071"}


id: GO:0004864
data:
  {"annotated_genes":["SJAG_04999","SJAG_02380","SJAG_03309","SJAG_04627","SJAG_03272"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70041,89140],"is_not":false,"summary":null,"term":"GO:0004864"},{"annotations":[87615,74417,75779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004865"}]},"cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of a protein phosphatase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase inhibitor activity","termid":"GO:0019212"},{"relation_name":"is_a","term_name":"protein phosphatase regulator activity","termid":"GO:0019888"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02380":null,"SJAG_03272":null,"SJAG_03309":null,"SJAG_04627":null,"SJAG_04999":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0004857"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0098772","GO:0004857","GO:0140678"],"is_obsolete":false,"name":"protein phosphatase inhibitor activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:1990681"],"synonyms":[{"name":"phosphoprotein phosphatase inhibitor activity","type":"exact"},{"name":"protein phosphatase 2 inhibitor activity","type":"narrow"},{"name":"protein phosphatase type 2A inhibitor activity","type":"narrow"}],"termid":"GO:0004864","terms_by_termid":{"GO:0004864":null,"GO:0004865":null}}


id: MONDO:0009300
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Perrault syndrome in which the cause of the disease is a mutation in the HSD17B4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Perrault syndrome","termid":"MONDO:0017312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005047"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0006025","MONDO:0005047","MONDO:0004069"],"is_obsolete":false,"name":"Perrault syndrome 1","secondary_identifiers":["MEDGEN:1640257","Orphanet:642945","OMIM:233400","UMLS:C4551721"],"synonyms":[{"name":"HSD17B4 Perrault syndrome","type":"exact"},{"name":"PRLTS1","type":"related"},{"name":"Perrault syndrome 1","type":"exact"},{"name":"Perrault syndrome caused by mutation in HSD17B4","type":"exact"},{"name":"Perrault syndrome type 1","type":"exact"},{"name":"gonadal dysgenesis, 20 type, with deafness","type":"related"},{"name":"ovarian dysgenesis with sensorineural deafness","type":"related"}],"termid":"MONDO:0009300","xrefs":{"Monarch":{"xref_id":"0009300"}}}


id: MONDO:0002365
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangiopericytoma arising from the kidney.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangiopericytoma","termid":"MONDO:0005094"},{"relation_name":"is_a","term_name":"kidney neoplasm","termid":"MONDO:0021163"}],"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":"kidney hemangiopericytoma","secondary_identifiers":["MEDGEN:1847044","DOID:262","SCTID:254923001","NCIT:C4527","UMLS:C5848097"],"synonyms":[{"name":"hemangiopericytoma of kidney","type":"exact"},{"name":"hemangiopericytoma of the kidney","type":"exact"},{"name":"kidney hemangiopericytoma","type":"exact"},{"name":"kidney spindle cell tumor","type":"exact"},{"name":"kidney spindle cell tumour","type":"exact"},{"name":"renal hemangiopericytoma","type":"exact"}],"termid":"MONDO:0002365","xrefs":{"Monarch":{"xref_id":"0002365"}}}


id: GO:0010434
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to a bract. This process pertains to the initial formation of a structure from unspecified parts. A bract is a leaf, usually different in form from the foliage leaves, subtending a flower or inflorescence.","definition_xrefs":["PMID:16554366","GOC:tb","PO:0009055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant organ formation","termid":"GO:1905393"},{"relation_name":"part_of","term_name":"bract morphogenesis","termid":"GO:0010433"}],"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":"bract formation","termid":"GO:0010434"}


id: GO:0005567
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cytosolic ribosomal RNA (obsolete GO:0005567)","synonyms":[{"name":"cytosolic ribosomal RNA","type":"exact"}],"termid":"GO:0005567"}


id: GO:0009136
data:
  {"annotated_genes":["SJAG_02038"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006172"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of purine nucleoside diphosphate, a compound consisting of a purine base linked to a ribose or deoxyribose sugar esterified with diphosphate on the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside diphosphate biosynthetic process","termid":"GO:0009133"},{"relation_name":"is_a","term_name":"purine nucleoside diphosphate metabolic process","termid":"GO:0009135"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02038":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"purine nucleoside diphosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"purine nucleoside diphosphate anabolism","type":"exact"},{"name":"purine nucleoside diphosphate biosynthesis","type":"exact"},{"name":"purine nucleoside diphosphate formation","type":"exact"},{"name":"purine nucleoside diphosphate synthesis","type":"exact"}],"termid":"GO:0009136","terms_by_termid":{"GO:0006172":null}}


id: PBO:0034349
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-derived_by_descent_from","termid":"PBO:0034349"}


id: GO:0018501
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the conversion of a di- or tetrachlorinated dienol to the corresponding catechol.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-chlorobenzene dihydrodiol dehydrogenase activity (obsolete GO:0018501)","termid":"GO:0018501"}


id: MONDO:0002309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Conjunctivitis that is characterized by the formation of papillae on the palpebral conjunctiva.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"conjunctivitis","termid":"MONDO:0003799"}],"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":"papillary conjunctivitis","secondary_identifiers":["ICD9:372.39","icd11.foundation:392841027","MEDGEN:167698","DOID:2458","NCIT:C35616","SCTID:416878008","UMLS:C0854165"],"termid":"MONDO:0002309","xrefs":{"Monarch":{"xref_id":"0002309"}}}


id: PBO:0116268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase of the DEAD-box protein family; strong preference for dsRNA; remodels RNP structure for efficient transcription termination; required for assembly of Yra1p, Nab2p and Mex67p onto mRNA and formation of nuclear mRNP; involved in mRNA decay and rRNA processing; may suppress transcription from cryptic initiation sites; promotes Mex67p-mediated nuclear export of mRNA by facilitating annealing with antisense RNAs to create dsRNAs; binds G-quadruplex (G4) nucleic acids","termid":"PBO:0116268"}


id: PBO:0069317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 575, pseudogene","termid":"PBO:0069317"}


id: PBO:0110826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, glucose starvation sensing, Rst2","termid":"PBO:0110826"}


id: MOD:01645
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes or replaces an L-proline.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue removal","termid":"MOD:01651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-proline removal","termid":"MOD:01645"}


id: FYPO:0002587
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 any mitochondrially-encoded polycistronic RNA precursors measured in the cell is higher than normal.","definition_xrefs":["PomBase:mah"],"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":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0006551","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased level of mitochondrial polycistronic RNA precursors","synonyms":[{"name":"increased accumulation of mitochondrial polycistronic RNA precursors","type":"related"},{"name":"increased level of mitochondrial polycistronic RNA precursors during mitotic cell cycle","type":"related"},{"name":"increased level of mitochondrial polycistronic RNA precursors during vegetative growth","type":"exact"}],"termid":"FYPO:0002587"}


id: GO:0106238
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction:peregrinol diphosphate = all-trans-geranylgeranyl diphosphate + H2O.","definition_xrefs":["PMID:29315936","PMID:24990389","RHEA:54652","GOC:emb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"peregrinol diphosphate synthase activity","secondary_identifiers":["EC:4.2.1.174"],"termid":"GO:0106238"}


id: GO:0035937
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of estrogen into the circulatory system. Estrogen is a steroid hormone that stimulates or controls the development and maintenance of female sex characteristics in mammals.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid hormone secretion","termid":"GO:0035929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"estrogen secretion","synonyms":[{"name":"oestrogen secretion","type":"related"}],"termid":"GO:0035937"}


id: PBO:0034061
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-immediate_transformation_of","termid":"PBO:0034061"}


id: GO:0035300
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reactions: ATP + 1D-myo-inositol 1,3,4-trisphosphate = ADP + 1D-myo-inositol 1,3,4,5-tetrakisphosphate, and ATP + 1D-myo-inositol 1,3,4-trisphosphate = ADP + 1D-myo-inositol 1,3,4,6-tetrakisphosphate.","definition_xrefs":["PMID:9126335"],"gene_count":0,"genotype_count":0,"name":"obsolete inositol-1,3,4-trisphosphate 5/6-kinase activity (obsolete GO:0035300)","synonyms":[{"name":"inositol 1,3,4-trisphosphate 5-kinase activity","type":"narrow"},{"name":"inositol 1,3,4-trisphosphate 6-kinase activity","type":"narrow"},{"name":"inositol-1,3,4-trisphosphate 5/6-kinase activity","type":"exact"}],"termid":"GO:0035300"}


id: GO:0002454
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The deletion of B cells by apoptotic process occurring as part of peripheral tolerance induction and B cell selection.","definition_xrefs":["ISBN:0781735149","GOC:mtg_apoptosis","GOC:jal","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell deletion","termid":"GO:0002516"},{"relation_name":"part_of","term_name":"peripheral B cell tolerance induction","termid":"GO:0002451"}],"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":"peripheral B cell deletion","synonyms":[{"name":"peripheral B lymphocyte deletion","type":"exact"},{"name":"peripheral B-cell deletion","type":"exact"},{"name":"peripheral B-lymphocyte deletion","type":"exact"}],"termid":"GO:0002454"}


id: MONDO:0017480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"amelia of lower limb","termid":"MONDO:0017438"}],"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":"amelia of lower limb, unilateral","secondary_identifiers":["Orphanet:295057","icd11.foundation:1342789404"],"termid":"MONDO:0017480","xrefs":{"Monarch":{"xref_id":"0017480"}}}


id: GO:0031711
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a bradykinin receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"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:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"bradykinin receptor binding","synonyms":[{"name":"bradykinin receptor ligand","type":"narrow"}],"termid":"GO:0031711"}


id: MONDO:0004702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The presence of whitish patches on the mucosal surface of the cervix. Histologic examination reveals hyperkeratosis. In a minority of cases, underlying dysplasia or carcinoma in situ is present.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervix disorder","termid":"MONDO:0002256"},{"relation_name":"is_a","term_name":"leukoplakia","termid":"MONDO:0043243"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterine cervix leukoplakia","secondary_identifiers":["SCTID:50923006","UMLS:C0269194","ICD10CM:N88.0","DOID:9043","ICD9:622.2","MEDGEN:124350","NCIT:C3976"],"synonyms":[{"name":"cervical leukoplakia","type":"exact"},{"name":"cervix leukoplakia","type":"exact"},{"name":"cervix uteri leukoplakia","type":"exact"},{"name":"leukoplakia of cervix","type":"exact"},{"name":"leukoplakia of cervix (uteri)","type":"exact"},{"name":"leukoplakia of cervix uteri","type":"exact"},{"name":"leukoplakia of the cervix","type":"exact"},{"name":"leukoplakia of the cervix uteri","type":"exact"},{"name":"leukoplakia of the uterine cervix","type":"exact"},{"name":"leukoplakia of uterine cervix","type":"exact"}],"termid":"MONDO:0004702","xrefs":{"Monarch":{"xref_id":"0004702"}}}


id: GO:2000418
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of eosinophil migration.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte migration","termid":"GO:0002687"},{"relation_name":"is_a","term_name":"regulation of eosinophil migration","termid":"GO:2000416"},{"relation_name":"positively_regulates","term_name":"eosinophil migration","termid":"GO:0072677"}],"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 eosinophil migration","termid":"GO:2000418"}


id: PBO:0113062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the kinetochore sub-complex COMA; COMA (Ctf19p, Okp1p, Mcm21p, Ame1p) bridges kinetochore subunits in contact with centromeric DNA with subunits bound to microtubules during kinetochore assembly; involved in minichromosome maintenance; modified by sumoylation; orthologous to human centromere constitutive-associated network (CCAN) subunit CENP-O","termid":"PBO:0113062"}


id: PR:Q9URT9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gsk31 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9URT9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase gsk31 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC8D2.01","synonyms":[{"name":"Spom972h-gsk31","type":"exact"}],"termid":"PR:Q9URT9"}


id: GO:0051970
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of transmission of a nerve impulse, the sequential electrochemical polarization and depolarization that travels across the membrane of a neuron in response to stimulation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell communication","termid":"GO:0010648"},{"relation_name":"is_a","term_name":"negative regulation of nervous system process","termid":"GO:0031645"},{"relation_name":"is_a","term_name":"regulation of transmission of nerve impulse","termid":"GO:0051969"},{"relation_name":"negatively_regulates","term_name":"transmission of nerve impulse","termid":"GO:0019226"}],"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 transmission of nerve impulse","synonyms":[{"name":"down regulation of transmission of nerve impulse","type":"exact"},{"name":"down-regulation of transmission of nerve impulse","type":"exact"},{"name":"downregulation of transmission of nerve impulse","type":"exact"},{"name":"inhibition of transmission of nerve impulse","type":"narrow"},{"name":"negative regulation of conduction of nerve impulse","type":"exact"}],"termid":"GO:0051970"}


id: PBO:0044583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dysbindin domain containing 1","termid":"PBO:0044583"}


id: GO:0075169
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism activates, maintains or increases the frequency, rate or extent of its protein kinase-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 positive regulation of symbiont protein kinase-mediated signal transduction in response to host (obsolete GO:0075169)","termid":"GO:0075169"}


id: SO:0001102
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A binding site that, in the polypeptide molecule, interacts selectively and non-covalently with tungsten ions.","definition_xrefs":["EBIBS:GAR","SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_metal_contact","termid":"SO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"polypeptide_tungsten_ion_contact_site","secondary_identifiers":["BS:00143"],"synonyms":[{"name":"W_contact_site","type":"exact"},{"name":"polypeptide tungsten ion contact site","type":"exact"}],"termid":"SO:0001102"}


id: MONDO:1011814
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cancer or benign tumor, non-human animal","termid":"MONDO:1011305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanoblastoma, non-human animal","secondary_identifiers":["OMIA:001324"],"termid":"MONDO:1011814","xrefs":{"Monarch":{"xref_id":"1011814"}}}


id: MONDO:1012565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dyserythropoietic anemia and myopathy syndrome, non-human animal","termid":"MONDO:1011708"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dyserythropoietic anemia and myopathy syndrome, dog","secondary_identifiers":["OMIA:002564-9615"],"termid":"MONDO:1012565","xrefs":{"Monarch":{"xref_id":"1012565"}}}


id: PBO:0060223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix remodeling associated 5","termid":"PBO:0060223"}


id: PBO:0003665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial RNA-binding protein (predicted)","termid":"PBO:0003665"}


id: MONDO:1012480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cervical vertebral compressive myelopathy, non-human animal","termid":"MONDO:1011891"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical vertebral compressive myelopathy, mountain zebra","secondary_identifiers":["OMIA:001894-9791"],"termid":"MONDO:1012480","xrefs":{"Monarch":{"xref_id":"1012480"}}}


id: MONDO:1011545
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Immunoglobulin A glomerulonephropathy that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerulonephritis, dog","termid":"MONDO:1011043"},{"relation_name":"is_a","term_name":"immunoglobulin A glomerulonephropathy, non-human animal","termid":"MONDO:1011449"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin A glomerulonephropathy, dog","secondary_identifiers":["OMIA:000553-9615"],"termid":"MONDO:1011545","xrefs":{"Monarch":{"xref_id":"1011545"}}}


id: PBO:0050918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IFITM3 pseudogene 1","termid":"PBO:0050918"}


id: PBO:0059516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded L-strand promoter","termid":"PBO:0059516"}


id: MONDO:0010293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"},{"relation_name":"is_a","term_name":"hypohidrotic ectodermal dysplasia","termid":"MONDO:0016535"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"ectodermal dysplasia and immune deficiency","secondary_identifiers":["NANDO:2200761","SCTID:703525006","MEDGEN:375786","Orphanet:98813","NCIT:C118844","UMLS:C1846006","DOID:0081077","MESH:C536181","GARD:9936","NANDO:1200360","OMIMPS:300291"],"synonyms":[{"name":"EDA-ID","type":"exact"},{"name":"HED-ID","type":"exact"},{"name":"Xhm-Ed","type":"related"},{"name":"anhidrotic ectodermal dysplasia with immune deficiency","type":"exact"},{"name":"anhidrotic ectodermal dysplasia with immunodeficiency","type":"exact"},{"name":"ectodermal dysplasia, anhidrotic, with immune deficiency","type":"related"},{"name":"ectodermal dysplasia, hypohidrotic, with immune deficiency","type":"related"},{"name":"hyper-IgM immunodeficiency, X-linked, with hypohidrotic ectodermal dysplasia","type":"related"},{"name":"hypohidrotic ectodermal dysplasia with immune deficiency","type":"exact"},{"name":"hypohidrotic ectodermal dysplasia with immunodeficiency","type":"exact"}],"termid":"MONDO:0010293","xrefs":{"Monarch":{"xref_id":"0010293"}}}


id: FYPO:0007582
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 duration of septation initiation network signaling is longer than normal. Signaling may continue after cytokinesis takes place.","definition_xrefs":["PomBase:mah","PomBase:vw","PMID:19736319"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal septation initiation network signaling","termid":"FYPO:0007569"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000298","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased duration of septation initiation network signaling","synonyms":[{"name":"increased duration of SIN signaling","type":"exact"},{"name":"increased duration of septation initiation network signaling during mitotic cell cycle","type":"related"},{"name":"increased duration of septation initiation network signaling during vegetative growth","type":"exact"},{"name":"increased duration of septation initiation network signalling","type":"exact"},{"name":"increased duration of septation initiation signaling","type":"exact"},{"name":"prolonged septation initiation network signaling","type":"exact"}],"termid":"FYPO:0007582"}


id: MONDO:0007126
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any spondyloarthropathy, susceptibility to in which the cause of the disease is a mutation in the HLA-B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloarthropathy, susceptibility to","termid":"MONDO:0024512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondyloarthropathy, susceptibility to, 1","secondary_identifiers":["DOID:0080603","MEDGEN:400145","UMLS:C1862852","OMIM:106300"],"synonyms":[{"name":"Bechterew syndrome","type":"related"},{"name":"HLA-B spondyloarthropathy, susceptibility to","type":"exact"},{"name":"Marie-Strumpell spondylitis","type":"related"},{"name":"SPDA1","type":"related"},{"name":"ankylosing spondylitis, susceptibility to","type":"related"},{"name":"spondyloarthropathy, susceptibility to caused by mutation in HLA-B","type":"exact"},{"name":"spondyloarthropathy, susceptibility to, 1","type":"exact"},{"name":"spondyloarthropathy, susceptibility to, type 1","type":"exact"},{"name":"susceptibility to spondyloarthropathy 1","type":"related"}],"termid":"MONDO:0007126","xrefs":{"Monarch":{"xref_id":"0007126"}}}


id: GO:1902241
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving copal-8-ol diphosphate(3-).","definition_xrefs":["PMID:22672125","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid metabolic process","termid":"GO:0006644"},{"relation_name":"is_a","term_name":"diterpenoid metabolic process","termid":"GO:0016101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"copal-8-ol diphosphate(3-) metabolic process","synonyms":[{"name":"copal-8-ol diphosphate(3-) metabolism","type":"exact"}],"termid":"GO:1902241"}


id: MONDO:0004354
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leukemia that occurs during the neonatal period.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood leukemia","termid":"MONDO:0004355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"neonatal leukemia","secondary_identifiers":["DOID:7756","UMLS:C0235813","MEDGEN:116003","NCIT:C3845"],"synonyms":[{"name":"neonatal leukemia","type":"exact"}],"termid":"MONDO:0004354","xrefs":{"Monarch":{"xref_id":"0004354"}}}


id: MONDO:0034099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete SYNGAP1-related developmental and epileptic encephalopathy (obsolete MONDO:0034099)","secondary_identifiers":["UMLS:C5680163","GARD:22232","MEDGEN:1810512"],"termid":"MONDO:0034099","xrefs":{"Monarch":{"xref_id":"0034099"}}}


id: MONDO:0015366
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal recessive form of hereditary sensory and autonomic neuropathy.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive hereditary sensory and autonomic neuropathy (obsolete MONDO:0015366)","secondary_identifiers":["Orphanet:140477"],"synonyms":[{"name":"hereditary sensory and autonomic neuropathy, autosomal recessive","type":"exact"}],"termid":"MONDO:0015366","xrefs":{"Monarch":{"xref_id":"0015366"}}}


id: GO:0071459
data:
  {"annotated_genes":["SJAG_04259","SJAG_03327","SJAG_02336","SJAG_01297","SJAG_02761","SJAG_03540","SJAG_04126"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77705,75072,59369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034501"},{"annotations":[100145,103657,108019,118407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140210"}]},"cv_name":"biological_process","definition":"Any process in which a protein is transported to, or maintained at, the centromeric region of a chromosome.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to chromosome","termid":"GO:0034502"}],"gene_count":7,"genes_by_uniquename":{"SJAG_01297":null,"SJAG_02336":null,"SJAG_02761":null,"SJAG_03327":null,"SJAG_03540":null,"SJAG_04126":null,"SJAG_04259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to chromosome, centromeric region","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"protein localisation to chromosome, centromeric region","type":"exact"},{"name":"protein localization to centromere","type":"exact"},{"name":"protein localization to chromosome, centric region","type":"exact"}],"termid":"GO:0071459","terms_by_termid":{"GO:0034501":null,"GO:0140210":null}}


id: GO:0045202
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The junction between an axon of one neuron and a dendrite of another neuron, a muscle fiber or a glial cell. As the axon approaches the synapse it enlarges into a specialized structure, the presynaptic terminal bouton, which contains mitochondria and synaptic vesicles. At the tip of the terminal bouton is the presynaptic membrane; facing it, and separated from it by a minute cleft (the synaptic cleft) is a specialized area of membrane on the receiving cell, known as the postsynaptic membrane. In response to the arrival of nerve impulses, the presynaptic terminal bouton secretes molecules of neurotransmitters into the synaptic cleft. These diffuse across the cleft and transmit the signal to the postsynaptic membrane.","definition_xrefs":["PMID:24619342","PMID:29383328","PMID:31998110","GOC:aruk","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell junction","termid":"GO:0030054"}],"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":"synapse","secondary_identifiers":["Wikipedia:Chemical_synapse","NIF_Subcellular:sao914572699"],"synonyms":[{"name":"electrotonic synapse","type":"related"},{"name":"mixed synapse","type":"narrow"},{"name":"synaptic junction","type":"exact"}],"termid":"GO:0045202"}


id: PBO:0049046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 37","termid":"PBO:0049046"}


id: PBO:0070006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1303, pseudogene","termid":"PBO:0070006"}


id: GO:1905564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of vascular endothelial cell proliferation.","definition_xrefs":["GOC:nc","GOC:TermGenie","GO_REF:0000058","PMID:23201774","GOC:BHF","GOC:BHF_telomere"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endothelial cell proliferation","termid":"GO:0001938"},{"relation_name":"is_a","term_name":"regulation of vascular endothelial cell proliferation","termid":"GO:1905562"},{"relation_name":"positively_regulates","term_name":"vascular endothelial cell proliferation","termid":"GO:0101023"}],"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 vascular endothelial cell proliferation","synonyms":[{"name":"activation of vascular endothelial cell proliferation","type":"narrow"},{"name":"up regulation of vascular endothelial cell proliferation","type":"exact"},{"name":"up-regulation of vascular endothelial cell proliferation","type":"exact"},{"name":"upregulation of vascular endothelial cell proliferation","type":"exact"}],"termid":"GO:1905564"}


id: GO:0045719
data:
  {"annotated_genes":["SJAG_01376","SJAG_00963"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76962,78661],"is_not":false,"summary":null,"term":"GO:0045719"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of glycogen.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glycogen biosynthetic process","termid":"GO:0005979"},{"relation_name":"is_a","term_name":"negative regulation of macromolecule biosynthetic process","termid":"GO:0010558"},{"relation_name":"is_a","term_name":"negative regulation of glycogen metabolic process","termid":"GO:0070874"},{"relation_name":"negatively_regulates","term_name":"glycogen biosynthetic process","termid":"GO:0005978"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00963":null,"SJAG_01376":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"negatively_regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0006091"],"is_obsolete":false,"name":"negative regulation of glycogen biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"down regulation of glycogen biosynthetic process","type":"exact"},{"name":"down-regulation of glycogen biosynthetic process","type":"exact"},{"name":"downregulation of glycogen biosynthetic process","type":"exact"},{"name":"inhibition of glycogen biosynthetic process","type":"narrow"},{"name":"negative regulation of glycogen anabolism","type":"exact"},{"name":"negative regulation of glycogen biosynthesis","type":"exact"},{"name":"negative regulation of glycogen formation","type":"exact"},{"name":"negative regulation of glycogen synthesis","type":"exact"}],"termid":"GO:0045719","terms_by_termid":{"GO:0045719":null}}


id: PBO:0085980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; protein-coding gene that evolved de novo via a series of point mutations in noncoding sequence; ORF exhibits genomic organization compatible with a translational readthrough-dependent mode of expression; readthrough is increased upon depletion of Sup35p; may be involved in DNA repair pathway during stationary phase and contribute to robustness of cells when shifted to a nutrient-poor environment","termid":"PBO:0085980"}


id: FYECO:0000185
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which sodium was added to the medium or assay buffers in a limiting quantity compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping limited","termid":"FYECO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ limited sodium","termid":"FYECO:0000185"}


id: GO:0008710
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-alanine + H+ + pimelyl-CoA = 8-amino-7-oxononanoate + CO2 + CoA.","definition_xrefs":["EC:2.3.1.47","RHEA:20712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016746","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"8-amino-7-oxononanoate synthase activity","secondary_identifiers":["MetaCyc:7KAPSYN-RXN","KEGG_REACTION:R03210"],"synonyms":[{"name":"6-carboxyhexanoyl-CoA:L-alanine C-carboxyhexanoyltransferase (decarboxylating)","type":"related"},{"name":"7-KAP synthetase activity","type":"related"},{"name":"7-keto-8-amino-pelargonic acid synthetase activity","type":"related"},{"name":"7-keto-8-aminopelargonic acid synthetase activity","type":"related"},{"name":"7-keto-8-aminopelargonic synthetase activity","type":"related"},{"name":"8-amino-7-ketopelargonate synthase activity","type":"related"},{"name":"8-amino-7-oxopelargonate synthase activity","type":"related"},{"name":"AONS activity","type":"related"}],"termid":"GO:0008710"}


id: MONDO:1010237
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polymicrogyria that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder, non-human animal","termid":"MONDO:1011308"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polymicrogyria, non-human animal","secondary_identifiers":["OMIA:001100"],"termid":"MONDO:1010237","xrefs":{"Monarch":{"xref_id":"1010237"}}}


id: PATO:0001936
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  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spheroid quality inhering in a bearer by virtue of the bearer's being egg-shaped and flat, with the narrow end attached to the base.","definition_xrefs":["wordreference:wordreference"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovate","termid":"PATO:0001891"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"obovate","synonyms":[{"name":"obovoid","type":"related"}],"termid":"PATO:0001936"}


id: GO:0001188
data:
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id: PBO:0052013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"JMJD1C antisense RNA 2","termid":"PBO:0052013"}


id: PBO:0070172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 86 pseudogene","termid":"PBO:0070172"}


id: PBO:0030264
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_N,N'-(p-xylylidene)bis-aminoguanidine_2HCl","termid":"PBO:0030264"}


id: GO:0071113
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id: GO:0102785
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: violaxanthin + 2 O2 = 2 5,6-epoxy-3-hydroxy-9-apo-beta-caroten-9-one + 4,9-dimethyldodeca-2,4,6,8,10-pentaenedial.","definition_xrefs":["GOC:pz","PMID:11316814"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"violaxanthin oxygenase activity","secondary_identifiers":["MetaCyc:RXN-7886"],"termid":"GO:0102785"}


id: GO:0046893
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The incorporation of iron into an L-cysteinyl diiron subcluster, found in Fe-hydrogenase.","definition_xrefs":["RESID:AA0334"],"gene_count":0,"genotype_count":0,"name":"obsolete iron incorporation into hydrogenase diiron subcluster via L-cysteine ligation (obsolete GO:0046893)","termid":"GO:0046893"}


id: PBO:0036208
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3_acetylation_during_vegetative_growth","termid":"PBO:0036208"}


id: PBO:0049126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor class C group 5 member C","termid":"PBO:0049126"}


id: PBO:0089972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-M, glycosylphosphatidylinositol-mannosyltransferase I complex subunit pig-M","termid":"PBO:0089972"}


id: PBO:0053834
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 1099","termid":"PBO:0053834"}


id: GO:0033554
data:
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id: FYPO:0009052
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population phenotype in which cell growth is increased relative to normal in a medium containing glutamate as the nitrogen source.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002057","FYPO:0002058","FYPO:0005447","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"increased cell population growth on glutamate nitrogen source","synonyms":[{"name":"increased growth on glutamate nitrogen source","type":"broad"},{"name":"increased vegetative cell growth on glutamate nitrogen source","type":"exact"}],"termid":"FYPO:0009052"}


id: MONDO:0001384
data:
  {"annotated_genes":["SJAG_04553","SJAG_03233"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85275],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032941"},{"annotations":[85816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012154"}]},"cv_name":"mondo","definition":"The condition in which the individual does not see far distances clearly.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"refractive error","termid":"MONDO:0004892"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03233":null,"SJAG_04553":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"myopia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1666440799","HP:0000545","UMLS:C0027092","SCTID:57190000","MESH:D009216","DOID:11830","ICD9:367.1","MEDGEN:44558","OMIMPS:160700","ICD10CM:H52.1"],"synonyms":[{"name":"myopia","type":"exact"},{"name":"myopia (disease)","type":"exact"},{"name":"near vision","type":"exact"},{"name":"near-sightedness","type":"exact"},{"name":"short-sightedness","type":"exact"}],"termid":"MONDO:0001384","terms_by_termid":{"MONDO:0012154":null,"MONDO:0032941":null},"xrefs":{"Monarch":{"xref_id":"0001384"}}}


id: PBO:0090393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clr6 histone deacetylase associated PHD finger protein Cph1","termid":"PBO:0090393"}


id: FYPO:0006760
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which centromeres do not detach properly from the spindle pole body (SPB) during the meiotic cell cycle. Normally, centromeres are located at the SPB during mitotic interphase, and upon entering meiosis, telomeres cluster at the SPB, followed by centromere detachment from the SPB.","definition_xrefs":["PomBase:mah","PMID:27611693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic chromosome organization","termid":"FYPO:0006759"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000641","FYPO:0000631","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal centromere detachment from spindle pole body during meiotic chromosome organization","synonyms":[{"name":"abnormal centromere detachment from SPB during meiotic chromosome organization","type":"exact"},{"name":"abnormal centromere detachment from spindle pole body during meiotic chromosome organisation","type":"exact"},{"name":"abnormal centromere detachment from spindle pole body involved in chromosome organization involved in meiotic cell cycle","type":"exact"},{"name":"abnormal centromere detachment from spindle pole body involved in meiotic chromosome organization","type":"exact"},{"name":"defective centromere detachment from the SPB during karyogamy and meiotic prophase","type":"exact"}],"termid":"FYPO:0006760"}


id: GO:1903937
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an acrylamide stimulus.","definition_xrefs":["GOC:TermGenie","GO_REF:0000071","PMID:16292499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to acrylamide","termid":"GO:1903937"}


id: FYPO:0006457
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at the central core of the centromeric regions is abolished during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization during meiotic cell cycle","termid":"FYPO:0005208"},{"relation_name":"is_a","term_name":"abolished protein localization to chromatin during meiosis I","termid":"FYPO:0006161"},{"relation_name":"is_a","term_name":"abnormal protein localization to centromere during meiotic cell cycle","termid":"FYPO:0006529"}],"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:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to centromere central core during meiosis I","synonyms":[{"name":"abolished protein localisation to centromere central core during meiosis I","type":"exact"},{"name":"abolished protein localisation to chromatin at centromere central core during meiosis I","type":"exact"},{"name":"abolished protein localization to centromere central core during first meiotic nuclear division","type":"exact"},{"name":"abolished protein localization to chromatin at centromere central core during meiosis I","type":"exact"},{"name":"protein localization to centromere central core abolished during meiosis I","type":"exact"},{"name":"protein localization to chromatin at centromere central core abolished during meiosis I","type":"exact"}],"termid":"FYPO:0006457"}


id: FYPO:0002052
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which the frequency of occurrence of ascospore formation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000003"],"is_obsolete":false,"name":"normal sporulation frequency","synonyms":[{"name":"normal ascospore formation frequency","type":"exact"},{"name":"normal sporulation occurrence","type":"exact"}],"termid":"FYPO:0002052"}


id: GO:2000073
data:
  {"annotated_genes":["SJAG_00845","SJAG_02392","SJAG_01787","SJAG_02380","SJAG_02838","SJAG_03309","SJAG_00256"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90532,110515,103456,119340],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903617"},{"annotations":[111124,87614,101144],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902472"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of site selection that occurs as part of cytokinesis.","definition_xrefs":["GOC:obol","GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokinetic process","termid":"GO:0032954"},{"relation_name":"regulates","term_name":"cytokinesis, division site positioning","termid":"GO:0007105"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00256":null,"SJAG_00845":null,"SJAG_01787":null,"SJAG_02380":null,"SJAG_02392":null,"SJAG_02838":null,"SJAG_03309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of cytokinesis, site selection","references_by_uniquename":{"GO_REF:0000107":null,"PMID:25866389":null},"synonyms":[{"name":"regulation of site selection involved in cell cycle cytokinesis","type":"exact"}],"termid":"GO:2000073","terms_by_termid":{"GO:1902472":null,"GO:1903617":null}}


id: FYPO:0005354
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 site-specific DNA replication termination at the RTS1 barrier in the mating type region is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal metabolic process during vegetative growth","termid":"FYPO:0000859"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal site-specific DNA replication termination at RTS1 barrier","synonyms":[{"name":"normal site-specific DNA replication termination at RTS1 barrier during mitotic cell cycle","type":"related"},{"name":"normal site-specific DNA replication termination at RTS1 barrier during vegetative growth","type":"exact"}],"termid":"FYPO:0005354"}


id: GO:0002654
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of tolerance induction dependent upon immune response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of tolerance induction","termid":"GO:0002645"},{"relation_name":"is_a","term_name":"regulation of tolerance induction dependent upon immune response","termid":"GO:0002652"},{"relation_name":"is_a","term_name":"positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains","termid":"GO:0002824"},{"relation_name":"positively_regulates","term_name":"tolerance induction dependent upon immune response","termid":"GO:0002461"}],"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 tolerance induction dependent upon immune response","synonyms":[{"name":"activation of tolerance induction dependent upon immune response","type":"narrow"},{"name":"positive regulation of immune response-dependent tolerance induction","type":"exact"},{"name":"stimulation of tolerance induction dependent upon immune response","type":"narrow"},{"name":"up regulation of tolerance induction dependent upon immune response","type":"exact"},{"name":"up-regulation of tolerance induction dependent upon immune response","type":"exact"},{"name":"upregulation of tolerance induction dependent upon immune response","type":"exact"}],"termid":"GO:0002654"}


id: GO:0021976
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Generation of a long process of a CNS neuron, that carries efferent (outgoing) action potentials from the cell body in the medulla towards target cells in the spinal cord.","definition_xrefs":["GOC:dph","GO_REF:0000021","GOC:dgh","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system projection neuron axonogenesis","termid":"GO:0021952"}],"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":"medulla reticulospinal tract morphogenesis","termid":"GO:0021976"}


id: GO:0034426
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Either of the lipid bilayers that surround a etioplast and form the etioplast envelope.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid membrane","termid":"GO:0042170"},{"relation_name":"part_of","term_name":"etioplast envelope","termid":"GO:0034425"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"etioplast membrane","termid":"GO:0034426"}


id: GO:0019148
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-cysteine + H2O = sulfide + NH3 + pyruvate.","definition_xrefs":["EC:4.4.1.15"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"D-cysteine desulfhydrase activity","secondary_identifiers":["MetaCyc:DCYSDESULF-RXN","RHEA:11268"],"synonyms":[{"name":"D-cysteine lyase activity","type":"related"},{"name":"D-cysteine sulfide-lyase (deaminating)","type":"related"},{"name":"D-cysteine sulfide-lyase (deaminating; pyruvate-forming)","type":"related"}],"termid":"GO:0019148"}


id: PBO:0016923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein Mug143","termid":"PBO:0016923"}


id: MONDO:0859309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"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":"spastic paraplegia 88, autosomal dominant","secondary_identifiers":["MEDGEN:1824020","DOID:0070457","UMLS:C5774247","OMIM:620106"],"termid":"MONDO:0859309","xrefs":{"Monarch":{"xref_id":"0859309"}}}


id: MONDO:0005011
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A gastrointestinal disorder characterized by chronic inflammation involving all layers of the intestinal wall, noncaseating granulomas affecting the intestinal wall and regional lymph nodes, and transmural fibrosis. Crohn disease most commonly involves the terminal ileum; the colon is the second most common site of involvement.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"Crohn disease","secondary_identifiers":["NANDO:1200444","Orphanet:206","EFO:0000384","icd11.foundation:1267652425","NANDO:1200446","MESH:D003424","NCIT:C2965","SCTID:34000006","ICD9:555.1","DOID:8778","MEDGEN:3664","NANDO:2200921","UMLS:C0010346","SCTID:7620006"],"synonyms":[{"name":"Crohn disease","type":"exact"},{"name":"Crohn's disease","type":"exact"},{"name":"Crohn's disease of colon","type":"exact"},{"name":"Crohn's disease of large bowel","type":"exact"},{"name":"granulomatous colitis","type":"exact"},{"name":"paediatric Crohn's disease","type":"exact"},{"name":"pediatric Crohn's disease","type":"exact"},{"name":"regional enteritis","type":"exact"}],"termid":"MONDO:0005011","xrefs":{"Monarch":{"xref_id":"0005011"}}}


id: PR:O74330
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 40S ribosomal protein S27-like protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02489","PANTHER:PTHR11594:SF0"],"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":"40S ribosomal protein S27 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1685.10","secondary_identifiers":["UniProtKB:O74330"],"synonyms":[{"name":"Spom972h-RPS27L","type":"exact"}],"termid":"PR:O74330"}


id: MONDO:0017189
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diazoxide-resistant hyperinsulism (DRH) is form of congenital isolated hyperinsulinism caused by an abnormal insulin production by b-cells in the pancreas that can be diffuse or focal and is characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia), recurrent episodes of profound hypoglycemia and resistance to medical management with diazoxide","definition_xrefs":["Orphanet:276608"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hyperinsulinism","termid":"MONDO:0017182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia","secondary_identifiers":["GARD:21056","SCTID:717044000","MEDGEN:907576","UMLS:C4274082"],"synonyms":[{"name":"NI-PHH","type":"exact"}],"termid":"MONDO:0017189","xrefs":{"Monarch":{"xref_id":"0017189"}}}


id: PBO:0089374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase Pyp2","termid":"PBO:0089374"}


id: GO:0001720
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification process that results in the conversion of lysine, carried by a specialized lysine-accepting tRNA (possessing a CUA anticodon), to pyrrolysine (a lysine with an amide linkage to a (4R,5R)-4-substituted pyrroline-5-carboxylate).","definition_xrefs":["PMID:12029132","PMID:12121639","PMID:12029131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"charged-tRNA amino acid modification","termid":"GO:0019988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006399","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"conversion of lysyl-tRNA to pyrrolysyl-tRNA","termid":"GO:0001720"}


id: MONDO:0044768
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant extra-adrenal parasympathetic paraganglioma arising from paraganglia in the vagus nerve. Patients may present with a slow growing, painless mass in the neck, hoarseness, vocal cord paralysis, and dysphagia.","definition_xrefs":["NCIT:C8427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vagus nerve neoplasm","termid":"MONDO:0001608"},{"relation_name":"is_a","term_name":"head and neck paraganglioma","termid":"MONDO:0006239"},{"relation_name":"is_a","term_name":"parasympathetic paraganglioma","termid":"MONDO:0021052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vagus nerve paraganglioma","secondary_identifiers":["GARD:8620","MEDGEN:141635","SCTID:253030004","UMLS:C0474819"],"synonyms":[{"name":"paraganglioma of the vagal body","type":"exact"},{"name":"paraganglioma of the vagus nerve","type":"exact"},{"name":"paraganglioma of vagal body","type":"exact"},{"name":"paraganglioma of vagus nerve","type":"exact"},{"name":"vagal body paraganglioma","type":"exact"},{"name":"vagal paraganglioma","type":"exact"},{"name":"vagus nerve paraganglioma","type":"exact"}],"termid":"MONDO:0044768","xrefs":{"Monarch":{"xref_id":"0044768"}}}


id: PBO:0084924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Monomeric glyoxalase I; catalyzes the detoxification of methylglyoxal (a by-product of glycolysis) via condensation with glutathione to produce S-D-lactoylglutathione; required for full activity of O-acetyl homoserine sulfhydrylase, Met17p; expression regulated by methylglyoxal levels and osmotic stress","termid":"PBO:0084924"}


id: PBO:0031031
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_plasma_membrane_organization","termid":"PBO:0031031"}


id: PBO:0076472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TANK antisense RNA 1","termid":"PBO:0076472"}


id: FYPO:0004210
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic spindle elongation begins, but mitotic sister chromatid segregation stops before completing separation of chromosomes, DNA remains in a single mass at or near the midpoint of the mitotic spindle, and centromeric DNA is not closely associated with the mitotic spindle.","definition_xrefs":["PomBase:mah","PomBase:vw","PMID:16855021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic spindle elongation without chromosome separation","termid":"FYPO:0003758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0000337","FYPO:0001985","FYPO:0000631"],"is_obsolete":false,"name":"mitotic spindle elongation without chromosome separation with centromeric DNA dissociated from spindle","synonyms":[{"name":"incomplete mitotic sister chromatid segregation, with unseparated DNA and centromeric DNA dissociated from spindle","type":"exact"},{"name":"mitotic spindle elongation without chromosome separation with centromeric DNA dissociated from spindle during vegetative growth","type":"exact"},{"name":"spindle elongation without chromosome separation with centromeric DNA dissociated from spindle during mitotic cell cycle","type":"related"}],"termid":"FYPO:0004210"}


id: PR:P0CT34
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- Tf2-1 gene.","definition_xrefs":["UniProtKB:P0CT34","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":"transposon Tf2-1 polyprotein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9.04","synonyms":[{"name":"Spom972h-Tf2-1","type":"exact"},{"name":"retrotransposable element Tf2 155 kDa protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P0CT34"}


id: PBO:0088343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial phosphatidic acid transfer protein Ups1","termid":"PBO:0088343"}


id: GO:0018156
data:
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id: PBO:0114351
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id: PBO:0084747
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id: GO:0006811
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id: MONDO:0002019
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id: PBO:0030367
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id: MONDO:1012453
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id: PBO:0065774
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id: MONDO:1011720
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id: PBO:0091194
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id: PBO:0054410
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id: PBO:0049283
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id: PBO:0004550
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id: GO:0017134
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id: GO:0097059
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id: PBO:0003226
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id: PBO:0017583
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id: PBO:0054442
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id: PBO:0065464
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id: MONDO:0004445
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare morphologic variant of bladder adenocarcinoma characterized by the presence of malignant glandular epithelial cells and clear cells forming a papillary pattern.","definition_xrefs":["NCIT:C39848"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bladder clear cell adenocarcinoma","termid":"MONDO:0003386"}],"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":"bladder papillary clear cell adenocarcinoma","secondary_identifiers":["DOID:8051","MEDGEN:307286","UMLS:C1511196"],"synonyms":[{"name":"bladder papillary clear cell adenocarcinoma","type":"exact"}],"termid":"MONDO:0004445","xrefs":{"Monarch":{"xref_id":"0004445"}}}


id: GO:1900396
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of kojic acid biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of kojic acid biosynthetic process","termid":"GO:1900394"},{"relation_name":"is_a","term_name":"positive regulation of alcohol biosynthetic process","termid":"GO:1902932"},{"relation_name":"positively_regulates","term_name":"kojic acid biosynthetic process","termid":"GO:2001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"positive regulation of kojic acid biosynthetic process","synonyms":[{"name":"activation of 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formation","type":"exact"},{"name":"activation of kojic acid synthesis","type":"exact"},{"name":"positive regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one anabolism","type":"exact"},{"name":"positive regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one biosynthesis","type":"exact"},{"name":"positive regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one biosynthetic process","type":"exact"},{"name":"positive regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one formation","type":"exact"},{"name":"positive regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one synthesis","type":"exact"},{"name":"positive regulation of C6H6O4 anabolism","type":"related"},{"name":"positive regulation of C6H6O4 biosynthesis","type":"related"},{"name":"positive regulation of C6H6O4 biosynthetic process","type":"related"},{"name":"positive regulation of C6H6O4 formation","type":"related"},{"name":"positive regulation of C6H6O4 synthesis","type":"related"},{"name":"positive regulation of kojic acid anabolism","type":"exact"},{"name":"positive regulation of kojic acid biosynthesis","type":"exact"},{"name":"positive regulation of kojic acid formation","type":"exact"},{"name":"positive regulation of kojic acid synthesis","type":"exact"},{"name":"up regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one anabolism","type":"exact"},{"name":"up regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one biosynthesis","type":"exact"},{"name":"up regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one biosynthetic process","type":"exact"},{"name":"up regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one formation","type":"exact"},{"name":"up regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one synthesis","type":"exact"},{"name":"up regulation of C6H6O4 anabolism","type":"related"},{"name":"up regulation of C6H6O4 biosynthesis","type":"related"},{"name":"up regulation of C6H6O4 biosynthetic process","type":"related"},{"name":"up regulation of C6H6O4 formation","type":"related"},{"name":"up regulation of C6H6O4 synthesis","type":"related"},{"name":"up regulation of kojic acid anabolism","type":"exact"},{"name":"up regulation of kojic acid biosynthesis","type":"exact"},{"name":"up regulation of kojic acid biosynthetic process","type":"exact"},{"name":"up regulation of kojic acid formation","type":"exact"},{"name":"up regulation of kojic acid synthesis","type":"exact"},{"name":"up-regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one anabolism","type":"exact"},{"name":"up-regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one biosynthesis","type":"exact"},{"name":"up-regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one biosynthetic process","type":"exact"},{"name":"up-regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one formation","type":"exact"},{"name":"up-regulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one synthesis","type":"exact"},{"name":"up-regulation of C6H6O4 anabolism","type":"related"},{"name":"up-regulation of C6H6O4 biosynthesis","type":"related"},{"name":"up-regulation of C6H6O4 biosynthetic process","type":"related"},{"name":"up-regulation of C6H6O4 formation","type":"related"},{"name":"up-regulation of C6H6O4 synthesis","type":"related"},{"name":"up-regulation of kojic acid anabolism","type":"exact"},{"name":"up-regulation of kojic acid biosynthesis","type":"exact"},{"name":"up-regulation of kojic acid biosynthetic process","type":"exact"},{"name":"up-regulation of kojic acid formation","type":"exact"},{"name":"up-regulation of kojic acid synthesis","type":"exact"},{"name":"upregulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one anabolism","type":"exact"},{"name":"upregulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one biosynthesis","type":"exact"},{"name":"upregulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one biosynthetic process","type":"exact"},{"name":"upregulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one formation","type":"exact"},{"name":"upregulation of 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one synthesis","type":"exact"},{"name":"upregulation of C6H6O4 anabolism","type":"related"},{"name":"upregulation of C6H6O4 biosynthesis","type":"related"},{"name":"upregulation of C6H6O4 biosynthetic process","type":"related"},{"name":"upregulation of C6H6O4 formation","type":"related"},{"name":"upregulation of C6H6O4 synthesis","type":"related"},{"name":"upregulation of kojic acid anabolism","type":"exact"},{"name":"upregulation of kojic acid biosynthesis","type":"exact"},{"name":"upregulation of kojic acid biosynthetic process","type":"exact"},{"name":"upregulation of kojic acid formation","type":"exact"},{"name":"upregulation of kojic acid synthesis","type":"exact"}],"termid":"GO:1900396"}


id: MONDO:0008854
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Bardet-Biedl syndrome that has material basis in homozygous mutation in the BBS1 gene on chromosome 11q13.","definition_xrefs":["DOID:0110123","PMID:20177705"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bardet-Biedl syndrome","termid":"MONDO:0015229"},{"relation_name":"is_a","term_name":"BBS1-related ciliopathy","termid":"MONDO:1040043"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Bardet-Biedl syndrome 1","secondary_identifiers":["MEDGEN:422452","OMIM:209900","GARD:820","MESH:C537909","UMLS:C2936862"],"synonyms":[{"name":"BBS1","type":"exact"},{"name":"Bardet-Biedl syndrome 1","type":"exact"},{"name":"Bardet-Biedl syndrome 1, modifier of","type":"exact"},{"name":"Bardet-Biedl syndrome type 1","type":"exact"}],"termid":"MONDO:0008854","xrefs":{"Monarch":{"xref_id":"0008854"}}}


id: PBO:0087244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine-rich, hydrophilic protein; overexpression suppresses growth defects of hap2, hap3, and hap4 mutants; expression is under glucose control; cotranscribed with NAM7 in a cyp1 mutant; ISF1 has a paralog, MBR1, that arose from the whole genome duplication","termid":"PBO:0087244"}


id: CHEBI:18291
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"manganese atom","termid":"CHEBI:18291"}


id: MONDO:0010059
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spinal muscular atrophy, type I, with congenital bone fractures (obsolete MONDO:0010059)","termid":"MONDO:0010059","xrefs":{"Monarch":{"xref_id":"0010059"}}}


id: PBO:0108953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM69 pseudogene 1","termid":"PBO:0108953"}


id: MONDO:1012198
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ocular squamous cell carcinoma, non-human animal","termid":"MONDO:1011812"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ocular squamous cell carcinoma, goat","secondary_identifiers":["OMIA:000735-9925"],"termid":"MONDO:1012198","xrefs":{"Monarch":{"xref_id":"1012198"}}}


id: MONDO:0004890
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary choroidal atrophy","termid":"MONDO:0004883"},{"relation_name":"is_a","term_name":"central areolar choroidal dystrophy","termid":"MONDO:0008982"}],"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":"partial central choroid dystrophy","secondary_identifiers":["UMLS:C0339427","ICD9:363.53","MEDGEN:573145","DOID:9822","NANDO:1200939","SCTID:193468002"],"synonyms":[{"name":"choroidal dystrophy, central areolar","type":"exact"},{"name":"circinate choroidal dystrophy","type":"related"},{"name":"partial central choroid dystrophy","type":"exact"},{"name":"partial central dystrophy of choroid","type":"related"}],"termid":"MONDO:0004890","xrefs":{"Monarch":{"xref_id":"0004890"}}}


id: MONDO:0000203
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Dehydrated hereditary stomatocytosis (obsolete MONDO:0000203)","termid":"MONDO:0000203","xrefs":{"Monarch":{"xref_id":"0000203"}}}


id: MONDO:1010038
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gingival hypertrophy that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mouth mucosa disorder, non-human animal","termid":"MONDO:1011334"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gingival hypertrophy, non-human animal","secondary_identifiers":["OMIA:000409"],"termid":"MONDO:1010038","xrefs":{"Monarch":{"xref_id":"1010038"}}}


id: FYPO:0007558
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 econazole.","definition_xrefs":["PomBase:mah","PMID:33223513"],"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:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0002060","FYPO:0000257","FYPO:0002057","FYPO:0000139","FYPO:0000003"],"is_obsolete":false,"name":"normal growth on econazole","synonyms":[{"name":"normal cell population growth in presence of econazole","type":"exact"},{"name":"normal cell population growth on ECZ","type":"exact"},{"name":"normal cell population growth on econazole","type":"exact"},{"name":"normal cellular response to econazole","type":"related"},{"name":"normal vegetative cell population growth on econazole","type":"exact"}],"termid":"FYPO:0007558"}


id: GO:0097479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a synaptic vesicle or vesicles are transported to, and/or maintained in, a specific location.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle localization","termid":"GO:0051648"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"synaptic vesicle localization","synonyms":[{"name":"establishment and maintenance of synaptic vesicle localization","type":"exact"},{"name":"establishment and maintenance of synaptic vesicle position","type":"exact"},{"name":"synaptic vesicle localisation","type":"exact"}],"termid":"GO:0097479"}


id: PBO:0061869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"one cut homeobox 1","termid":"PBO:0061869"}


id: PBO:0077518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 233","termid":"PBO:0077518"}


id: PBO:0082195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alkaline dihydroceramidase, involved in sphingolipid metabolism; preferentially hydrolyzes dihydroceramide to a free fatty acid and dihydrosphingosine; has a minor reverse activity; YDC1 has a paralog, YPC1, that arose from the whole genome duplication","termid":"PBO:0082195"}


id: FYPO:0001502
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 trehalose measured in a cell is higher than normal during a cellular response to osmotic stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular trehalose level during vegetative growth","termid":"FYPO:0001444"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular trehalose level during cellular response to osmotic stress","synonyms":[{"name":"increased cellular trehalose level during cellular response to osmotic stress during mitotic cell cycle","type":"related"},{"name":"increased cellular trehalose level during vegetative growth and during cellular response to osmotic stress","type":"exact"},{"name":"increased cellular trehalose level in response to osmotic stress","type":"exact"},{"name":"increased trehalose accumulation during cellular response to osmotic stress","type":"related"}],"termid":"FYPO:0001502"}


id: GO:0033008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of mast cell activation as part of an immune response.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mast cell activation","termid":"GO:0033005"},{"relation_name":"is_a","term_name":"regulation of mast cell activation involved in immune response","termid":"GO:0033006"},{"relation_name":"is_a","term_name":"positive regulation of immune response","termid":"GO:0050778"},{"relation_name":"positively_regulates","term_name":"mast cell activation involved in immune response","termid":"GO:0002279"}],"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 mast cell activation involved in immune response","synonyms":[{"name":"positive regulation of mast cell activation during immune response","type":"related"}],"termid":"GO:0033008"}


id: PBO:0055460
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 2893","termid":"PBO:0055460"}


id: FYPO:0003529
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that enters the cell cycle and undergoes two or more rounds of cell division, but then becomes elongated and undergoes cell cycle arrest in interphase of the mitotic cell cycle, and eventually dies.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, multiple cell divisions, elongated cell","termid":"FYPO:0002262"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001985","FYPO:0001320","FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"inviable after spore germination, multiple cell divisions, cell cycle arrest in mitotic interphase, elongated cells","synonyms":[{"name":"inviable after spore germination, multiple cell divisions, elongated aseptate cell","type":"exact"},{"name":"inviable after spore germination, multiple cell divisions, elongated cell arrested at interphase","type":"exact"},{"name":"inviable germinated spore, multiple cell divisions, cell cycle arrest in mitotic interphase, elongated cells","type":"exact"},{"name":"lethal after spore germination, multiple cell divisions, cell cycle arrest in mitotic interphase, elongated cells","type":"exact"}],"termid":"FYPO:0003529"}


id: GO:0032025
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 cobalt ion (Co2+) stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to metal ion","termid":"GO:0010038"}],"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 cobalt ion","termid":"GO:0032025"}


id: MONDO:0003290
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"focal epilepsy","termid":"MONDO:0005384"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"simple partial epilepsy","secondary_identifiers":["DOID:5129","ICD9:345.51"],"termid":"MONDO:0003290","xrefs":{"Monarch":{"xref_id":"0003290"}}}


id: MONDO:0019527
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune disorder which does not meet classification criteria used to establish the presence of other well-defined connective tissue diseases.","definition_xrefs":["NCIT:C116776"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"undifferentiated connective tissue syndrome","secondary_identifiers":["Orphanet:90002","GARD:19097","MedDRA:10071575","MEDGEN:592754","UMLS:C0409999","SCTID:239918008"],"synonyms":[{"name":"UCTD","type":"exact"},{"name":"undifferentiated connective tissue disease","type":"exact"}],"termid":"MONDO:0019527","xrefs":{"Monarch":{"xref_id":"0019527"}}}


id: PBO:0077181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toll like receptor 5","termid":"PBO:0077181"}


id: PBO:0073285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 14 pseudogene 6","termid":"PBO:0073285"}


id: PBO:0064360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"premelanosome protein","termid":"PBO:0064360"}


id: MONDO:0957230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited oocyte maturation defect","termid":"MONDO:0014769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"oocyte/zygote/embryo maturation arrest 18","secondary_identifiers":["UMLS:C5830441","MEDGEN:1841077","OMIM:620332"],"termid":"MONDO:0957230","xrefs":{"Monarch":{"xref_id":"0957230"}}}


id: PATO:0001567
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial pattern inhering in a bearer by virtue of the bearer's not being spread out or scattered about or divided up.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spatial pattern","termid":"PATO:0000060"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"undistributed","termid":"PATO:0001567"}


id: GO:0018985
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Synthesis and ordering of the envelope of pronuclei.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear envelope organization","termid":"GO:0006998"},{"relation_name":"part_of","term_name":"single fertilization","termid":"GO:0007338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"pronuclear envelope synthesis","termid":"GO:0018985"}


id: PBO:0040538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-1,3-galactosyltransferase 5","termid":"PBO:0040538"}


id: GO:0120233
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to prenyl-FMNH2, a flavin mononucleotide obtained by prenylation of the N-10 position of FMNH2 followed by cyclisation. An essential cofactor for the decarboxylase enzymes UbiD and Fdc1.","definition_xrefs":["PMID:26083743","GOC:krc","PMID:26083754","PMID:25647642"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleotide binding","termid":"GO:0032553"},{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"prenyl-FMNH2 binding","synonyms":[{"name":"prenylated FMNH2 binding","type":"exact"}],"termid":"GO:0120233"}


id: PBO:0068169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 476","termid":"PBO:0068169"}


id: PBO:0004657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complexed with Cdc5 protein Cwf4","termid":"PBO:0004657"}


id: PBO:0074395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 5","termid":"PBO:0074395"}


id: MONDO:0004145
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A WHO grade I meningioma characterized by the presence of tumor cells that form lobules. The tumor cells are generally uniform. Whorls and psammoma bodies are usually not present.","definition_xrefs":["NCIT:C4329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meningothelial meningioma","secondary_identifiers":["ICDO:9531/0","DOID:7212","MEDGEN:90814","UMLS:C0334605"],"synonyms":[{"name":"Meningotheliomatous meningioma","type":"exact"},{"name":"meningothelial meningioma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0004145","xrefs":{"Monarch":{"xref_id":"0004145"}}}


id: MONDO:0021334
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disorders characterized by abnormal proliferation of primary cells of the immune system or by excessive production of immunoglobulins.","definition_xrefs":["MESH:D007160"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"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":"immunoproliferative disorder","secondary_identifiers":["UMLS:C0021070","SCTID:127071007","ICD9:203.80","MEDGEN:7038"],"synonyms":[{"name":"Disorder, Immunoproliferative","type":"related"},{"name":"Disorders, Immunoproliferative","type":"related"},{"name":"Immunoproliferative Disorder","type":"related"},{"name":"Immunoproliferative Disorders","type":"related"},{"name":"Immunoproliferative disease","type":"related"},{"name":"Immunoproliferative disorder","type":"related"},{"name":"immunoproliferative disorder","type":"exact"}],"termid":"MONDO:0021334","xrefs":{"Monarch":{"xref_id":"0021334"}}}


id: PBO:0001587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial hydrogen/potassium transport system protein (predicted)","termid":"PBO:0001587"}


id: MONDO:0958204
data:
  {"annotated_genes":["SJAG_00898"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86861],"is_not":false,"summary":null,"term":"MONDO:0958204"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00898":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"intellectual developmental disorder, autosomal recessive 81","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5882758","MEDGEN:1844192","OMIM:620700"],"termid":"MONDO:0958204","terms_by_termid":{"MONDO:0958204":null},"xrefs":{"Monarch":{"xref_id":"0958204"}}}


id: GO:0016962
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete receptor-associated protein activity (obsolete GO:0016962)","synonyms":[{"name":"receptor-associated protein activity","type":"exact"}],"termid":"GO:0016962"}


id: FYPO:0003013
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 contractile ring disassembly is abnormal. Contractile ring disassembly is the part of cytokinesis in which the actomyosin contractile ring is disaggregated into its constituent components.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cytokinesis","termid":"FYPO:0000032"},{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring organization","termid":"FYPO:0004738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000032","FYPO:0000002","FYPO:0004803","FYPO:0000631","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abnormal actomyosin contractile ring disassembly","synonyms":[{"name":"abnormal actomyosin contractile ring disassembly during mitotic cell cycle","type":"related"},{"name":"abnormal actomyosin contractile ring disassembly during vegetative growth","type":"exact"},{"name":"abnormal contractile ring disassembly","type":"exact"},{"name":"abnormal cytokinesis, actomyosin contractile ring disassembly","type":"exact"},{"name":"abnormal cytokinetic contractile ring disassembly","type":"exact"},{"name":"abnormal cytokinetic ring disassembly","type":"related"},{"name":"abnormal mitotic actomyosin contractile ring disassembly","type":"exact"},{"name":"abnormal mitotic contractile ring disassembly","type":"exact"}],"termid":"FYPO:0003013"}


id: PBO:0031700
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_nuclear_fusion_during_mating","termid":"PBO:0031700"}


id: PBO:0013075
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements E. coli hisI","termid":"PBO:0013075"}


id: MONDO:0100311
data:
  {"annotated_genes":["SJAG_01854"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012166"}]},"cv_name":"mondo","definition":"Any ataxia in which the causes of the disease is a perturbation of the sensory system, leading to its dysfunction.","definition_xrefs":["PMID:32965955","MONDO:patterns/disease_by_dysfunctional_structure"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atactic disorder","termid":"MONDO:0100308"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01854":null},"genotype_count":0,"is_obsolete":false,"name":"sensory ataxia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:66020","UMLS:C0240991"],"termid":"MONDO:0100311","terms_by_termid":{"MONDO:0012166":null},"xrefs":{"Monarch":{"xref_id":"0100311"}}}


id: PBO:0084130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hexokinase isoenzyme 2; phosphorylates glucose in cytosol; predominant hexokinase during growth on glucose; represses expression of HXK1, GLK1, induces expression of its own gene; antiapoptotic; phosphorylation/dephosphorylation at Ser14 by kinase Snf1p, phosphatase Glc7p-Reg1p regulates nucleocytoplasmic shuttling of Hxk2p; functions downstream of Sit4p in control of cell cycle, mitochondrial function, oxidative stress resistance, chronological lifespan; has paralog HXK1","termid":"PBO:0084130"}


id: PATO:0000855
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000855 corneal reflex value (obsolete PATO:0000855)","termid":"PATO:0000855"}


id: PBO:0089391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation regulator, HEAT repeat protein Gcn1","termid":"PBO:0089391"}


id: PBO:0026681
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cell_population_growth_on_maltose_carbon_source","termid":"PBO:0026681"}


id: GO:0099623
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the establishment or extent of a change in membrane potential in the polarizing direction towards the resting potential in a cardiomyocyte.","definition_xrefs":["GOC:BHF","GOC:rl","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane repolarization","termid":"GO:0060306"},{"relation_name":"regulates","term_name":"cardiac muscle cell membrane repolarization","termid":"GO:0099622"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cardiac muscle cell membrane repolarization","synonyms":[{"name":"heart repolarization","type":"related"},{"name":"regulation of cardiac muscle cell repolarization","type":"exact"},{"name":"regulation of cardiomyocyte membrane repolarization","type":"exact"}],"termid":"GO:0099623"}


id: GO:0099018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont evades the DNA restriction modification system of its host. This process occurs in phages to protein themselves from bacterial restriction enzyme systems. Some viruses encode their own methyltransferase in order to protect their genome from host restriction enzymes. Others directly inhibit restriction enzymes while some use unusual bases in their genome to avoid restriction.","definition_xrefs":["PMID:24123737","VZ:3966","PMID:23979432","PMID:20348932"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated evasion of recognition by host innate immune effector","termid":"GO:0141177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated evasion of host restriction-modification system","synonyms":[{"name":"evasion by virus of host restriction-modification system","type":"related"},{"name":"evasion of host restriction-modification system","type":"exact"},{"name":"restriction-modification system evasion by virus","type":"exact"}],"termid":"GO:0099018"}


id: GO:1902276
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of pancreatic amylase secretion.","definition_xrefs":["GOC:jc","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein secretion","termid":"GO:0050708"},{"relation_name":"regulates","term_name":"pancreatic amylase secretion","termid":"GO:0036395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of pancreatic amylase secretion","termid":"GO:1902276"}


id: PBO:0001417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calchone related protein family","termid":"PBO:0001417"}


id: MONDO:0015397
data:
  {"annotated_genes":["SJAG_00539","SJAG_00322"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85498,85499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958175"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic developmental defect of the eye (obsolete MONDO:0015218)","termid":"MONDO:0015218"},{"relation_name":"excluded_subClassOf","term_name":"obsolete branchial arch or oral-acral syndrome (obsolete MONDO:0015334)","termid":"MONDO:0015334"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic palpebral coloboma (obsolete MONDO:0020157)","termid":"MONDO:0020157"},{"relation_name":"excluded_subClassOf","term_name":"obsolete bulbar conjunctival dermoid or conjunctival dermolipoma (obsolete MONDO:0020205)","termid":"MONDO:0020205"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic corneal dystrophy (obsolete MONDO:0020215)","termid":"MONDO:0020215"},{"relation_name":"excluded_subClassOf","term_name":"obsolete lens shape anomaly (obsolete MONDO:0020237)","termid":"MONDO:0020237"},{"relation_name":"excluded_subClassOf","term_name":"obsolete genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability (obsolete MONDO:0043008)","termid":"MONDO:0043008"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"oculoauriculovertebral spectrum with radial defects","termid":"MONDO:0007712"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00322":null,"SJAG_00539":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"craniofacial microsomia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:75554","Orphanet:141132","MESH:D006053","UMLS:C0265240","DOID:2907","SCTID:367462009","Orphanet:374","SCTID:109393007","GARD:12074","NCIT:C84740","Orphanet:141136","ICD9:759.89","OMIMPS:164210"],"synonyms":[{"name":"Expanded spectrum hemifacial microsomia","type":"exact"},{"name":"Expanded spectrum of hemifacial microsomia","type":"exact"},{"name":"Fav sequence","type":"related"},{"name":"Goldenhar disease","type":"exact"},{"name":"Goldenhar syndrome","type":"exact"},{"name":"HFM","type":"exact"},{"name":"Laterofacial microsomia","type":"exact"},{"name":"OAV (oculoauriculovertebral) dysplasia","type":"exact"},{"name":"OAV dysplasia","type":"exact"},{"name":"OAV spectrum","type":"exact"},{"name":"OAVD","type":"related"},{"name":"OAVS","type":"exact"},{"name":"facio-auriculo-vertebral spectrum","type":"exact"},{"name":"facioauriculovertebral dysplasia","type":"exact"},{"name":"facioauriculovertebral sequence","type":"related"},{"name":"first and second branchial arch syndrome","type":"exact"},{"name":"first arch syndrome","type":"exact"},{"name":"first branchial arch syndrome","type":"exact"},{"name":"hemifacial microsomia","type":"exact"},{"name":"oculo-auriculo-vertebral dysplasia","type":"related"},{"name":"oculo-auriculo-vertebral spectrum","type":"exact"},{"name":"oculoauriculovertebral dysplasia","type":"exact"},{"name":"oculoauriculovertebral spectrum","type":"exact"},{"name":"oculoauriculovertebral syndrome","type":"exact"},{"name":"otomandibular syndrome","type":"exact"},{"name":"unilateral or bilateral and asymmetric otomandibular dysplasia","type":"exact"}],"termid":"MONDO:0015397","terms_by_termid":{"MONDO:0958175":null},"xrefs":{"Monarch":{"xref_id":"0015397"}}}


id: PBO:0055498
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 2932","termid":"PBO:0055498"}


id: PBO:0070957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18a pseudogene 12","termid":"PBO:0070957"}


id: GO:0160080
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + indole(in) = ADP + phosphate + indole(out).","definition_xrefs":["PMID:37146609"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ABC-type indole transporter activity","termid":"GO:0160080"}


id: PBO:0069401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 661, pseudogene","termid":"PBO:0069401"}


id: PBO:0076219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfite oxidase","termid":"PBO:0076219"}


id: MONDO:0014972
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosome 19q13.11 deletion syndrome in which the proximal region was deleted.","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 19q13.11 deletion syndrome","termid":"MONDO:0013090"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 19q13.11 deletion syndrome, proximal","secondary_identifiers":["OMIM:617219","UMLS:C4311046","MEDGEN:935013"],"termid":"MONDO:0014972","xrefs":{"Monarch":{"xref_id":"0014972"}}}


id: GO:0008552
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: Me2+(in) + ATP = Me2+(out) + ADP + phosphate, where Me is Zn2+, Cd2+, Co2+, Ni2+ or Pb2+.","definition_xrefs":["TC:3.A.3.6.2"],"gene_count":0,"genotype_count":0,"name":"obsolete zinc, cadmium, cobalt, nickel, lead-efflux ATPase activity (obsolete GO:0008552)","synonyms":[{"name":"zinc, cadmium, cobalt, nickel, lead-efflux ATPase activity","type":"exact"}],"termid":"GO:0008552"}


id: PBO:0054234
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 1616","termid":"PBO:0054234"}


id: FYPO:0000532
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of mitotic cell cycle arrest in response to pheromone is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle arrest in response to pheromone","termid":"FYPO:0000530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0000298"],"is_obsolete":false,"name":"decreased mitotic cell cycle arrest in response to pheromone","synonyms":[{"name":"decreased pheromone-induced mitotic cell cycle arrest","type":"exact"},{"name":"pheromone-induced cell cycle arrest: decreased","type":"related"},{"name":"reduced mitotic cell cycle arrest in response to pheromone","type":"exact"}],"termid":"FYPO:0000532"}


id: PBO:0039325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arachidonate 12-lipoxygenase pseudogene 2","termid":"PBO:0039325"}


id: PBO:0108578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome large subunit export factor","termid":"PBO:0108578"}


id: GO:1904286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein-pyridoxal-5-phosphate linkage.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:25957689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein modification process","termid":"GO:0031400"},{"relation_name":"is_a","term_name":"regulation of protein-pyridoxal-5-phosphate linkage","termid":"GO:1904285"},{"relation_name":"negatively_regulates","term_name":"protein-pyridoxal-5-phosphate linkage","termid":"GO:0018352"}],"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-pyridoxal-5-phosphate linkage","synonyms":[{"name":"down regulation of protein-pyridoxal-5-phosphate linkage","type":"exact"},{"name":"down-regulation of protein-pyridoxal-5-phosphate linkage","type":"exact"},{"name":"downregulation of protein-pyridoxal-5-phosphate linkage","type":"exact"},{"name":"inhibition of protein-pyridoxal-5-phosphate linkage","type":"narrow"}],"termid":"GO:1904286"}


id: MONDO:0004965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the acinar cell","direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"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":"acinar cell carcinoma","secondary_identifiers":["icd11.foundation:1322159869","UMLS:C0206685","NCIT:C3768","ONCOTREE:ACCC","DOID:3025","EFO:0000216","MESH:D018267","MEDGEN:61660","ICDO:8550/3"],"synonyms":[{"name":"ACCC","type":"related"},{"name":"acinar adenocarcinoma","type":"exact"},{"name":"acinar carcinoma","type":"exact"},{"name":"acinar cell adenocarcinoma","type":"exact"},{"name":"acinar cell carcinoma","type":"exact"},{"name":"acinar cell carcinoma (morphologic abnormality)","type":"exact"},{"name":"acinic cell adenocarcinoma","type":"exact"},{"name":"acinic cell carcinoma","type":"exact"},{"name":"acinic cell tumor","type":"related"},{"name":"acinic cell tumour","type":"related"},{"name":"carcinoma of acinar cell","type":"exact"},{"name":"carcinoma, acinar cell, malignant","type":"exact"}],"termid":"MONDO:0004965","xrefs":{"Monarch":{"xref_id":"0004965"}}}


id: MONDO:0015093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nodular neuronal heterotopia","termid":"MONDO:0016292"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sub-cortical nodular heterotopia","secondary_identifiers":["GARD:19775","MEDGEN:1843064","UMLS:C5681805","icd11.foundation:1683302159","Orphanet:101029"],"termid":"MONDO:0015093","xrefs":{"Monarch":{"xref_id":"0015093"}}}


id: FYPO:0003857
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to mevastatin. Cells stop growing (and may die) at a concentration of mevastatin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0001985","FYPO:0005447","FYPO:0000003","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to mevastatin","synonyms":[{"name":"hypersensitive to mevastatin","type":"exact"},{"name":"sensitive to compactin","type":"exact"},{"name":"sensitive to mevastatin during mitotic cell cycle","type":"related"},{"name":"sensitive to mevastatin during vegetative growth","type":"exact"}],"termid":"FYPO:0003857"}


id: PBO:0056176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAF1 pseudogene 1","termid":"PBO:0056176"}


id: PBO:0077933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPTE2 pseudogene 6","termid":"PBO:0077933"}


id: PBO:0042689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cat eye syndrome chromosome region, candidate 3","termid":"PBO:0042689"}


id: MONDO:0023581
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"cleft lip","termid":"MONDO:0004747"},{"relation_name":"is_a","term_name":"cleft palate","termid":"MONDO:0016064"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kuster syndrome","secondary_identifiers":["GARD:3152","MEDGEN:419150","MESH:C538126","UMLS:C2931741"],"synonyms":[{"name":"cleft lip and palate, lower lip pits, and limb deficiency defects","type":"related"},{"name":"cleft lip palate lip pits limb deficiency","type":"related"}],"termid":"MONDO:0023581","xrefs":{"Monarch":{"xref_id":"0023581"}}}


id: SO:0000057
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A regulatory element of an operon to which activators or repressors bind thereby effecting translation of genes in that operon.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcriptional_cis_regulatory_region","termid":"SO:0001055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"operator","secondary_identifiers":["http://en.wikipedia.org/wiki/Operator_(biology)#Operator"],"synonyms":[{"name":"operator segment","type":"exact"}],"termid":"SO:0000057"}


id: GO:0042372
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phylloquinone, vitamin K1, a quinone-derived compound synthesized by green plants.","definition_xrefs":["PMID:27337968","PMID:23821151","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin K biosynthetic process","termid":"GO:0042371"},{"relation_name":"is_a","term_name":"phylloquinone metabolic process","termid":"GO:0042374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006766"],"is_obsolete":false,"name":"phylloquinone biosynthetic process","secondary_identifiers":["MetaCyc:PWY-5027"],"synonyms":[{"name":"phylloquinone anabolism","type":"exact"},{"name":"phylloquinone biosynthesis","type":"exact"},{"name":"phylloquinone formation","type":"exact"},{"name":"phylloquinone synthesis","type":"exact"},{"name":"phytomenadione biosynthesis","type":"exact"},{"name":"phytomenadione biosynthetic process","type":"exact"},{"name":"phytonadione biosynthesis","type":"exact"},{"name":"phytonadione biosynthetic process","type":"exact"},{"name":"phytylmenaquinone biosynthesis","type":"exact"},{"name":"phytylmenaquinone biosynthetic process","type":"exact"},{"name":"vitamin K1 biosynthesis","type":"exact"},{"name":"vitamin K1 biosynthetic process","type":"exact"}],"termid":"GO:0042372"}


id: PBO:0114869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [2Fe-2S] cluster assembly co-chaperone Jac1","termid":"PBO:0114869"}


id: PBO:0077026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymocyte selection associated","termid":"PBO:0077026"}


id: PBO:0086195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that activates Rub1p (NEDD8) before neddylation; acts together with Uba3p; may play a role in protein degradation","termid":"PBO:0086195"}


id: GO:0050467
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = diphosphate + pentalenene.","definition_xrefs":["RHEA:18081","EC:4.2.3.7"],"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:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"pentalenene synthase activity","secondary_identifiers":["MetaCyc:PENTALENENE-SYNTHASE-RXN","KEGG_REACTION:R02305"],"synonyms":[{"name":"2-trans,6-trans-farnesyl-diphosphate diphosphate-lyase (cyclizing, pentalenene-forming)","type":"related"},{"name":"2-trans,6-trans-farnesyldiphosphate diphosphate-lyase (cyclizing, pentalenene-forming)","type":"related"},{"name":"pentalenene synthetase activity","type":"related"}],"termid":"GO:0050467"}


id: PBO:0050526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"haptoglobin","termid":"PBO:0050526"}


id: PBO:0036389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ORMDL family protein Orm1 (predicted)","termid":"PBO:0036389"}


id: PBO:0018225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sec14 cytosolic factor family, glycerophospholipid-transfer protein (predicted)","termid":"PBO:0018225"}


id: GO:0018590
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: methylsilanetriol + O2 + 2 H+ + 2 e- = H2O + hydroxymethylsilanetriol.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete methylsilanetriol hydroxylase activity (obsolete GO:0018590)","termid":"GO:0018590"}


id: PATO:0001340
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A biological sex quality inhering in an organism or a population with both male and female sexual organs in one individual.","definition_xrefs":["MGED:MGED"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenotypic sex","termid":"PATO:0001894"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hermaphrodite","synonyms":[{"name":"intersex","type":"exact"}],"termid":"PATO:0001340"}


id: PBO:0087236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Separase/separin, a caspase-like cysteine protease; cleaves Mcd1p/Scc1p, a mitotic cohesin complex subunit, resulting in the dissociation of cohesin from chromatin and sister chromatid separation; cleaves meiotic-cohesin subunit Rec8p along chromosome arms in meiosis I and at centromeric sites during meiosis II; inhibits PP2A-Cdc55p to promote mitotic exit; inhibited by Pds1p (securin); relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0087236"}


id: MONDO:0020068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"infectious encephalitis","termid":"MONDO:0020067"},{"relation_name":"is_a","term_name":"post-infectious disorder","termid":"MONDO:0021669"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postinfectious encephalitis","secondary_identifiers":["MedDRA:10057235","MEDGEN:581376","SCTID:192727001","DOID:10993","Orphanet:98253","ICD9:323.6","UMLS:C0393459"],"termid":"MONDO:0020068","xrefs":{"Monarch":{"xref_id":"0020068"}}}


id: PBO:0088335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L22","termid":"PBO:0088335"}


id: MONDO:0859168
data:
  {"annotated_genes":["SJAG_01665"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86106],"is_not":false,"summary":null,"term":"MONDO:0859168"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myofibrillar myopathy","termid":"MONDO:0018943"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01665":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5561937","MEDGEN:1794147","OMIM:619424"],"termid":"MONDO:0859168","terms_by_termid":{"MONDO:0859168":null},"xrefs":{"Monarch":{"xref_id":"0859168"}}}


id: GO:0080126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the ovary septum over time, from its formation to the mature structure. The ovary septum is the thin partition that divides the ovary, the basal portion of a carpel or group of fused carpels, that encloses the ovule(s).","definition_xrefs":["PMID:17855426"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"plant septum development","termid":"GO:1905328"},{"relation_name":"part_of","term_name":"plant-type ovary development","termid":"GO:0035670"}],"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":"ovary septum development","termid":"GO:0080126"}


