# terms

id: GO:0015061
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 red-sensitive opsin (obsolete GO:0015061)","synonyms":[{"name":"red-sensitive opsin","type":"exact"}],"termid":"GO:0015061"}


id: PBO:0083024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Deleted ORF; does not encode a protein; originally included in genome annotation, but later deleted due to sequence correction","termid":"PBO:0083024"}


id: GO:0047130
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-saccharopine + H2O + NADP+ = 2-oxoglutarate + L-lysine + H+ + NADPH.","definition_xrefs":["EC:1.5.1.8","RHEA:19373"],"direct_ancestors":[{"relation_name":"is_a","term_name":"saccharopine dehydrogenase activity","termid":"GO:0004753"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"saccharopine dehydrogenase (NADP+, L-lysine-forming) activity","secondary_identifiers":["GO:0010010","Reactome:R-HSA-70938","KEGG_REACTION:R00716","MetaCyc:1.5.1.8-RXN"],"synonyms":[{"name":"6-N-(L-1,3-dicarboxypropyl)-L-lysine:NADP+ oxidoreductase (L-lysine-forming)","type":"related"},{"name":"L-lysine-alpha-ketoglutarate reductase activity","type":"related"},{"name":"N6-(L-1,3-dicarboxypropyl)-L-lysine:NADP+ oxidoreductase (L-lysine-forming)","type":"related"},{"name":"lysine:alpha-ketoglutarate:TPNH oxidoreductase (epsilon-N-[gultaryl-2]-L-lysine forming)","type":"related"},{"name":"saccharopine (nicotinamide adenine dinucleotide phosphate, lysine-forming) dehydrogenase activity","type":"related"}],"termid":"GO:0047130"}


id: PBO:0043333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calmin","termid":"PBO:0043333"}


id: PBO:0004658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Tma20 (predicted)","termid":"PBO:0004658"}


id: PBO:0059545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded tRNA-Leu (CUN) 2","termid":"PBO:0059545"}


id: GO:0050057
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + 2-hydroxy-2-methylpropanenitrile = UDP + linamarin.","definition_xrefs":["MetaCyc:LINAMARIN-SYNTHASE-RXN","EC:2.4.1.63"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glycosyltransferase activity","termid":"GO:0008194"},{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"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"}],"interesting_parent_ids":["GO:0016757","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"linamarin synthase activity","secondary_identifiers":["RHEA:20009"],"synonyms":[{"name":"UDP glucose ketone cyanohydrin glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:2-hydroxy-2-methylpropanenitrile beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:2-hydroxy-2-methylpropanenitrile beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:ketone cyanohydrin beta-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphate-glucose-ketone cyanohydrin beta-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-ketone cyanohydrin glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-ketone glucosyltransferase activity","type":"related"}],"termid":"GO:0050057"}


id: GO:0008915
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,3-bis(3-hydroxytetradecanoyl)-beta-D-glucosaminyl 1-phosphate + UDP-2,3-bis(3-hydroxytetradecanoyl)-D-glucosamine = 2,3-bis(3-hydroxytetradecanoyl)-D-glucosaminyl-(1->6)-beta-D-2,3-bis(3-hydroxytetradecanoyl)-beta-D-glucosaminyl 1-phosphate + H+ + UDP.","definition_xrefs":["EC:2.4.1.182","RHEA:22668"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glycosyltransferase activity","termid":"GO:0008194"},{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"lipid-A-disaccharide synthase activity","secondary_identifiers":["KEGG_REACTION:R04606","MetaCyc:LIPIDADISACCHARIDESYNTH-RXN"],"synonyms":[{"name":"UDP-2,3-bis(3-hydroxytetradecanoyl)glucosamine:2,3-bis-(3-hydroxytetradecanoyl)-beta-D-glucosaminyl-1-phosphate 2,3-bis(3-hydroxytetradecanoyl)-glucosaminyltransferase activity","type":"related"}],"termid":"GO:0008915"}


id: GO:0018115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of cysteine to form peptidyl-S-diphytanylglycerol diether-L-cysteine.","definition_xrefs":["PMID:7797461","RESID:AA0223"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-S-diphytanylglycerol diether-L-cysteine biosynthetic process from peptidyl-cysteine (obsolete GO:0018115)","synonyms":[{"name":"peptidyl-S-diphytanylglycerol diether-L-cysteine anabolism from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-diphytanylglycerol diether-L-cysteine formation from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-diphytanylglycerol diether-L-cysteine synthesis from peptidyl-cysteine","type":"exact"}],"termid":"GO:0018115"}


id: PR:O94356
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- meu6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94356"],"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":"meiotic expression up-regulated protein 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC428.07","synonyms":[{"name":"Spom972h-meu6","type":"exact"}],"termid":"PR:O94356"}


id: PBO:0002144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF654 family protein","termid":"PBO:0002144"}


id: PBO:0081501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 402, pseudogene","termid":"PBO:0081501"}


id: GO:0050138
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + NADP+ + nicotinate = 6-hydroxynicotinate + H+ + NADPH.","definition_xrefs":["RHEA:12236","EC:1.17.1.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH or CH2 groups, NAD or NADP as acceptor","termid":"GO:0016726"}],"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":"nicotinate dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN-7637","KEGG_REACTION:R01720"],"synonyms":[{"name":"nicotinate hydroxylase activity","type":"related"},{"name":"nicotinate:NADP+ 6-oxidoreductase (hydroxylating)","type":"related"},{"name":"nicotinic acid hydroxylase activity","type":"related"}],"termid":"GO:0050138"}


id: PBO:0051285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1-32 (pseudogene)","termid":"PBO:0051285"}


id: GO:0070231
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process in a T cell, a type of lymphocyte whose defining characteristic is the expression of a T cell receptor complex.","definition_xrefs":["ISBN:0781765196","GOC:mtg_apoptosis","GOC:add","CL:0000084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphocyte apoptotic process","termid":"GO:0070227"}],"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":"T cell apoptotic process","synonyms":[{"name":"T cell apoptosis","type":"narrow"},{"name":"T lymphocyte apoptosis","type":"exact"},{"name":"T-cell apoptosis","type":"exact"},{"name":"T-lymphocyte apoptosis","type":"exact"},{"name":"programmed cell death of T cells by apoptosis","type":"exact"}],"termid":"GO:0070231"}


id: MONDO:0011113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Charcot-Marie-Tooth disease type 4C (CMT4C) is a subtype of Charcot-Marie-Tooth type 4 characterized by childhood or adolescent-onset of a relatively mild, demyelinating sensorimotor neuropathy that contrasts with a severe, rapidly progressing, early-onset scoliosis, and the typical CMT phenotype (i.e. distal muscle weakness and atrophy, sensory loss, and often foot deformity). A wide spectrum of nerve conduction velocities are observed and cranial nerve involvement and kyphoscoliosis have also been reported.","definition_xrefs":["Orphanet:99949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 4","termid":"MONDO:0018995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease type 4C","secondary_identifiers":["MESH:C535423","MEDGEN:356581","OMIM:601596","NCIT:C129864","SCTID:715797002","icd11.foundation:382219984","GARD:9201","UMLS:C1866636","DOID:0110183"],"synonyms":[{"name":"CMT 4C","type":"related"},{"name":"CMT4C","type":"exact"},{"name":"Charcot Marie Tooth disease type 4C","type":"related"},{"name":"Charcot-Marie-Tooth disease type 4 caused by mutation in SH3TC2","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 4C","type":"exact"},{"name":"Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4C","type":"related"},{"name":"Charcot-Marie-Tooth disease, type 4C","type":"related"},{"name":"Charcot-Marie-Tooth neuropathy type 4C","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 4C","type":"related"},{"name":"SH3TC2 Charcot-Marie-Tooth disease type 4","type":"exact"},{"name":"autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4C","type":"exact"}],"termid":"MONDO:0011113","xrefs":{"Monarch":{"xref_id":"0011113"}}}


id: PBO:0030550
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histidine_import","termid":"PBO:0030550"}


id: MONDO:1030010
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cerebrovascular disorder characterized by an abnormal narrowing of a precerebral artery.","definition_xrefs":["SCTID:1055001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebrovascular disorder","termid":"MONDO:0011057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"precerebral artery stenosis","secondary_identifiers":["UMLS:C0265089","MEDGEN:539068","ICD10CM:I65"],"synonyms":[{"name":"narrowing of precerebral artery","type":"exact"}],"termid":"MONDO:1030010","xrefs":{"Monarch":{"xref_id":"1030010"}}}


id: GO:0061367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in the behaviour of an organism as a result of an acetic acid pain stimulus.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavioral response to chemical pain","termid":"GO:0061366"}],"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":"behavioral response to acetic acid induced pain","termid":"GO:0061367"}


id: MONDO:1011432
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Beta-mannosidosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease, non-human animal","termid":"MONDO:1010171"},{"relation_name":"is_a","term_name":"peripheral neuropathy, non-human animal","termid":"MONDO:1010239"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis, non-human animal","termid":"MONDO:1011310"},{"relation_name":"is_a","term_name":"hereditary neurological disease, non-human animal","termid":"MONDO:1012972"},{"relation_name":"is_a","term_name":"skeletal dysplasia, non-human animal","termid":"MONDO:1012973"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-mannosidosis, non-human animal","secondary_identifiers":["OMIA:000626"],"termid":"MONDO:1011432","xrefs":{"Monarch":{"xref_id":"1011432"}}}


id: MONDO:0020624
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete blood group--waldner type (obsolete MONDO:0020624)","secondary_identifiers":["OMIM:112010"],"synonyms":[{"name":"BLOOD GROUP--WALDNER TYPE","type":"related"},{"name":"WD","type":"related"},{"name":"Waldner Blood Group Antigen","type":"related"},{"name":"blood group, Waldner","type":"exact"}],"termid":"MONDO:0020624","xrefs":{"Monarch":{"xref_id":"0020624"}}}


id: GO:1904452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of hydrogen:potassium-exchanging ATPase activity.","definition_xrefs":["GOC:TermGenie","GO_REF:0000059","PMID:11897793"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of potassium:proton exchanging ATPase activity (obsolete GO:1904452)","synonyms":[{"name":"down regulation of (K+ + H+)-ATPase activity","type":"exact"},{"name":"down regulation of ATP phosphohydrolase (H+/K+-exchanging)","type":"exact"},{"name":"down regulation of H+-K+-ATPase activity","type":"exact"},{"name":"down regulation of H+/K(+)-ATPase activity","type":"exact"},{"name":"down regulation of H+/K(+)-exchanging ATPase activity","type":"exact"},{"name":"down regulation of H+/K+-ATPase activity","type":"exact"},{"name":"down regulation of H+/K+-exchanging ATPase activity","type":"exact"},{"name":"down regulation of H,K-ATPase activity","type":"exact"},{"name":"down regulation of gastric H+/K(+) ATPase activity","type":"narrow"},{"name":"down regulation of gastric H+/K+ ATPase","type":"narrow"},{"name":"down regulation of hydrogen/potassium-exchanging ATPase activity","type":"exact"},{"name":"down regulation of hydrogen:potassium exchanging ATPase activity","type":"exact"},{"name":"down regulation of hydrogen:potassium-exchanging ATPase activity","type":"exact"},{"name":"down-regulation of (K+ + H+)-ATPase activity","type":"exact"},{"name":"down-regulation of ATP phosphohydrolase (H+/K+-exchanging)","type":"exact"},{"name":"down-regulation of H+-K+-ATPase activity","type":"exact"},{"name":"down-regulation of H+/K(+)-ATPase activity","type":"exact"},{"name":"down-regulation of H+/K(+)-exchanging ATPase activity","type":"exact"},{"name":"down-regulation of H+/K+-ATPase activity","type":"exact"},{"name":"down-regulation of H+/K+-exchanging ATPase activity","type":"exact"},{"name":"down-regulation of H,K-ATPase activity","type":"exact"},{"name":"down-regulation of gastric H+/K(+) ATPase activity","type":"narrow"},{"name":"down-regulation of gastric H+/K+ ATPase","type":"narrow"},{"name":"down-regulation of hydrogen/potassium-exchanging ATPase activity","type":"exact"},{"name":"down-regulation of hydrogen:potassium exchanging ATPase activity","type":"exact"},{"name":"down-regulation of hydrogen:potassium-exchanging ATPase activity","type":"exact"},{"name":"downregulation of (K+ + H+)-ATPase activity","type":"exact"},{"name":"downregulation of ATP phosphohydrolase (H+/K+-exchanging)","type":"exact"},{"name":"downregulation of H+-K+-ATPase activity","type":"exact"},{"name":"downregulation of H+/K(+)-ATPase activity","type":"exact"},{"name":"downregulation of H+/K(+)-exchanging ATPase activity","type":"exact"},{"name":"downregulation of H+/K+-ATPase activity","type":"exact"},{"name":"downregulation of H+/K+-exchanging ATPase activity","type":"exact"},{"name":"downregulation of H,K-ATPase activity","type":"exact"},{"name":"downregulation of gastric H+/K(+) ATPase activity","type":"narrow"},{"name":"downregulation of gastric H+/K+ ATPase","type":"narrow"},{"name":"downregulation of hydrogen/potassium-exchanging ATPase activity","type":"exact"},{"name":"downregulation of hydrogen:potassium exchanging ATPase activity","type":"exact"},{"name":"downregulation of hydrogen:potassium-exchanging ATPase activity","type":"exact"},{"name":"inhibition of (K+ + H+)-ATPase activity","type":"narrow"},{"name":"inhibition of ATP phosphohydrolase (H+/K+-exchanging)","type":"narrow"},{"name":"inhibition of H+-K+-ATPase activity","type":"narrow"},{"name":"inhibition of H+/K(+)-ATPase activity","type":"narrow"},{"name":"inhibition of H+/K(+)-exchanging ATPase activity","type":"narrow"},{"name":"inhibition of H+/K+-ATPase activity","type":"narrow"},{"name":"inhibition of H+/K+-exchanging ATPase activity","type":"narrow"},{"name":"inhibition of H,K-ATPase activity","type":"narrow"},{"name":"inhibition of gastric H+/K(+) ATPase activity","type":"narrow"},{"name":"inhibition of gastric H+/K+ ATPase","type":"narrow"},{"name":"inhibition of hydrogen/potassium-exchanging ATPase activity","type":"narrow"},{"name":"inhibition of hydrogen:potassium exchanging ATPase activity","type":"narrow"},{"name":"inhibition of hydrogen:potassium-exchanging ATPase activity","type":"narrow"},{"name":"negative regulation of (K+ + H+)-ATPase activity","type":"exact"},{"name":"negative regulation of ATP phosphohydrolase (H+/K+-exchanging)","type":"exact"},{"name":"negative regulation of H+-K+-ATPase activity","type":"exact"},{"name":"negative regulation of H+/K(+)-ATPase activity","type":"exact"},{"name":"negative regulation of H+/K(+)-exchanging ATPase activity","type":"exact"},{"name":"negative regulation of H+/K+-ATPase activity","type":"exact"},{"name":"negative regulation of H+/K+-exchanging ATPase activity","type":"exact"},{"name":"negative regulation of H,K-ATPase activity","type":"exact"},{"name":"negative regulation of gastric H+/K(+) ATPase activity","type":"narrow"},{"name":"negative regulation of gastric H+/K+ ATPase","type":"narrow"},{"name":"negative regulation of hydrogen/potassium-exchanging ATPase activity","type":"exact"},{"name":"negative regulation of hydrogen:potassium exchanging ATPase activity","type":"exact"},{"name":"negative regulation of hydrogen:potassium-exchanging ATPase activity","type":"exact"}],"termid":"GO:1904452"}


id: GO:1904755
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of gut granule assembly.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:17535251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organelle assembly","termid":"GO:1902115"},{"relation_name":"regulates","term_name":"gut granule assembly","termid":"GO:1902900"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of gut granule assembly","synonyms":[{"name":"regulation of gut granule biogenesis","type":"exact"},{"name":"regulation of gut granule formation","type":"exact"}],"termid":"GO:1904755"}


id: PBO:0017520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial NAD transmembrane transporter Yea6 (predicted)","termid":"PBO:0017520"}


id: PBO:0041257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1 open reading frame 216","termid":"PBO:0041257"}


id: MONDO:0015272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Camptodactyly-taurinuria syndrome is a congenital malformation syndrome characterized by the association of a permanent camptodactyly of the fingers with the over excretion of taurine in the urine. Camptodactyly mainly affects the little finger, although any finger may be involved. The disease has been described in 17 affected patients from 4 unrelated families. An autosomal dominant inheritance has been suggested. There have been no further descriptions in the literature since 1966.","definition_xrefs":["Orphanet:1325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"camptodactyly-taurinuria syndrome","secondary_identifiers":["MESH:C537972","SCTID:733466005","MEDGEN:419871","UMLS:C2931681","GARD:1069"],"synonyms":[{"name":"camptodactyly taurinuria","type":"related"},{"name":"camptodactyly with taurinuria","type":"related"},{"name":"familial streblodactyly with amino-aciduria","type":"exact"}],"termid":"MONDO:0015272","xrefs":{"Monarch":{"xref_id":"0015272"}}}


id: GO:0097018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A renal system process in which albumin is taken up from the collecting ducts, glomerulus and proximal and distal loops of the nephron.","definition_xrefs":["GOC:yaf","PMID:18431508"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal protein absorption","termid":"GO:0097017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal albumin absorption","termid":"GO:0097018"}


id: FYPO:0007517
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 chromatin moves within the nucleus to a greater extent than normal.","definition_xrefs":["PMID:33153481","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin organization during vegetative growth","termid":"FYPO:0001352"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000641","FYPO:0001320"],"is_obsolete":false,"name":"increased chromatin mobility","synonyms":[{"name":"increased chromatin mobility during mitotic cell cycle","type":"related"},{"name":"increased chromatin mobility during vegetative growth","type":"exact"},{"name":"increased chromatin motility","type":"exact"},{"name":"increased chromatin movement","type":"exact"}],"termid":"FYPO:0007517"}


id: MONDO:0008184
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic agenesis","termid":"MONDO:0009832"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pancreas, dorsal, agenesis of","secondary_identifiers":["GARD:15104","MESH:C538109","MEDGEN:357024","OMIM:167755","UMLS:C1868659"],"synonyms":[{"name":"agenesis of the dorsal pancreas","type":"related"},{"name":"complete agenesis of the dorsal pancreas","type":"related"},{"name":"congenital short pancreas","type":"related"},{"name":"pancreas agenesis, dorsal","type":"related"},{"name":"pancreas, dorsal, agenesis of","type":"exact"},{"name":"partial agenesis of the dorsal pancreas","type":"related"}],"termid":"MONDO:0008184","xrefs":{"Monarch":{"xref_id":"0008184"}}}


id: GO:0043913
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A trimeric protein complex which in E. coli is composed of the subunits MreB, MreC and MreD. The complex directs longitudinal cell wall synthesis, maintaining cell morphology.","definition_xrefs":["PMID:15612918","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete chromosome segregation-directing complex (obsolete GO:0043913)","synonyms":[{"name":"MreBCD complex","type":"narrow"},{"name":"chromosome segregation directing complex","type":"exact"},{"name":"longitudinal peptidoglycan synthesis-directing complex","type":"exact"}],"termid":"GO:0043913"}


id: PBO:0047226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 228 member B","termid":"PBO:0047226"}


id: PBO:0061794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"odontogenic, ameloblast associated","termid":"PBO:0061794"}


id: PBO:0056866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule associated monooxygenase, calponin and LIM domain containing 2","termid":"PBO:0056866"}


id: PBO:0079372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin alpha pseudogene 7","termid":"PBO:0079372"}


id: PATO:0000146
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality of the thermal energy of a system.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"temperature","termid":"PATO:0000146"}


id: GO:0047177
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-alkyl-2-lyso-sn-glycero-3-phosphoethanolamine + 1-alkyl-2-arachidonyl-sn-glycero-3-phosphocholine = 1-alkyl-2-lyso-sn-glycero-3-phosphocholine + 1-alkyl-2-arachidonyl-sn-glycero-3-phosphoethanolamine.","definition_xrefs":["EC:2.3.1.147","MetaCyc:2.3.1.147-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016746"],"is_obsolete":false,"name":"glycerophospholipid arachidonoyl-transferase (CoA-independent) activity","secondary_identifiers":["RHEA:15409"],"synonyms":[{"name":"1-organyl-2-arachidonoyl-sn-glycero-3-phosphocholine:1-organyl-2-lyso-sn-glycero-3-phosphoethanolamine arachidonoyltransferase (CoA-independent)","type":"related"},{"name":"1-organyl-2-arachidonyl-sn-glycero-3-phosphocholine:1-organyl-2-lyso-sn-glycero-3-phosphoethanolamine arachidonoyltransferase (CoA-independent)","type":"related"}],"termid":"GO:0047177"}


id: PBO:0078343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (CTC) 9-1","termid":"PBO:0078343"}


id: GO:0097333
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 olanzapine stimulus.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to olanzapine","termid":"GO:0097333"}


id: FYPO:0005575
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"Auxotrophy in which a cell requires magnesium ions in the medium for vegetative cell growth.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxotrophy","termid":"FYPO:0000128"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype","termid":"FYPO:0004638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"growth auxotrophic for magnesium","synonyms":[{"name":"growth auxotrophic for magnesium during mitotic cell cycle","type":"related"},{"name":"growth auxotrophic for magnesium during vegetative growth","type":"exact"},{"name":"growth auxotrophic for magnesium ion","type":"exact"},{"name":"magnesium auxotrophy","type":"exact"}],"termid":"FYPO:0005575"}


id: GO:0070914
data:
  {"annotated_genes":["SJAG_00814","SJAG_01648","SJAG_02334","SJAG_02200","SJAG_04877","SJAG_00272","SJAG_01010","SJAG_02182","SJAG_00863","SJAG_00208","SJAG_04190","SJAG_01262","SJAG_05197","SJAG_02818","SJAG_00729","SJAG_02199","SJAG_04150","SJAG_02828","SJAG_03898"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60311,65061,66005,66647,67864,69185,70439,76010,88353,94006,96350,97453,104545,106267,113135],"is_not":false,"summary":null,"term":"GO:0070914"},{"annotations":[77250,95571,103142,109420],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"}]},"cv_name":"biological_process","definition":"A DNA repair process that is initiated by an endonuclease that introduces a single-strand incision immediately 5' of a UV-induced damage site. UV-damage excision repair acts on both cyclobutane pyrimidine dimers (CPDs) and pyrimidine-pyrimidone 6-4 photoproducts (6-4PPs).","definition_xrefs":["GOC:mah","PMID:9619100"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA repair","termid":"GO:0006281"},{"relation_name":"is_a","term_name":"cellular response to UV","termid":"GO:0034644"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00208":null,"SJAG_00272":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00863":null,"SJAG_01010":null,"SJAG_01262":null,"SJAG_01648":null,"SJAG_02182":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02334":null,"SJAG_02818":null,"SJAG_02828":null,"SJAG_03898":null,"SJAG_04150":null,"SJAG_04190":null,"SJAG_04877":null,"SJAG_05197":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006281"}],"interesting_parent_ids":["GO:0006281","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"UV-damage excision repair","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"AER","type":"related"},{"name":"UV-damaged DNA endonuclease-dependent excision repair","type":"exact"},{"name":"UVDE-dependent excision repair","type":"exact"},{"name":"UVER","type":"exact"},{"name":"alternative excision repair","type":"related"}],"termid":"GO:0070914","terms_by_termid":{"GO:0070914":null,"GO:1904161":null}}


id: MONDO:0013568
data:
  {"annotated_genes":["SJAG_02431","SJAG_03703"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87656,87657],"is_not":false,"summary":null,"term":"MONDO:0013568"}]},"cv_name":"mondo","definition":"Any familial sick sinus syndrome in which the cause of the disease is a mutation in the MYH6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02431":null,"SJAG_03703":null},"genotype_count":0,"is_obsolete":false,"name":"sick sinus syndrome 3, susceptibility to","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:481421","UMLS:C3279791","OMIM:614090"],"synonyms":[{"name":"MYH6 familial sick sinus syndrome","type":"exact"},{"name":"SSS3","type":"related"},{"name":"familial sick sinus syndrome caused by mutation in MYH6","type":"exact"},{"name":"sick sinus syndrome 3","type":"exact"},{"name":"sick sinus syndrome 3, susceptibility to","type":"exact"},{"name":"susceptibility to sick sinus syndrome 3","type":"related"}],"termid":"MONDO:0013568","terms_by_termid":{"MONDO:0013568":null},"xrefs":{"Monarch":{"xref_id":"0013568"}}}


id: PBO:0066501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"raftlin family member 2","termid":"PBO:0066501"}


id: GO:1990150
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A homodimeric, extracellular protein complex containing two VEGF-A monomers. Binds to and activates a receptor tyrosine kinase.","definition_xrefs":["GOC:bf","GOC:bhm","PMID:12207021","PMID:19658168"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor complex","termid":"GO:0036454"}],"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":"VEGF-A complex","synonyms":[{"name":"vascular endothelial growth factor A complex","type":"exact"}],"termid":"GO:1990150"}


id: PBO:0040628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B cell scaffold protein with ankyrin repeats 1","termid":"PBO:0040628"}


id: GO:0004987
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Combining with an opioid to initiate a change in cell activity, with the pharmacological characteristics of kappa-opioid receptors, including high affinity for dynorphins.","definition_xrefs":["IUPHAR_RECEPTOR:318"],"gene_count":0,"genotype_count":0,"name":"obsolete kappa-opioid receptor activity (obsolete GO:0004987)","secondary_identifiers":["Wikipedia:Kappa_Opioid_receptor"],"synonyms":[{"name":"kappa-opioid receptor activity","type":"exact"}],"termid":"GO:0004987"}


id: PBO:0065740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paxillin","termid":"PBO:0065740"}


id: PBO:0072392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS27A pseudogene 18","termid":"PBO:0072392"}


id: PBO:0048996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPC5 antisense RNA 2","termid":"PBO:0048996"}


id: FYPO:0004115
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an inviable cell that does not divide, and that has a septum with abnormal size, shape, or structure and a nucleus that is larger than normal.","definition_xrefs":["PomBase:mah","PMID:15116432"],"direct_ancestors":[{"relation_name":"has_part","term_name":"enlarged nucleus during vegetative growth","termid":"FYPO:0000344"},{"relation_name":"is_a","term_name":"enlarged nucleus during vegetative growth","termid":"FYPO:0000344"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, abnormal septum morphology","termid":"FYPO:0004114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0002403"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000032","FYPO:0000004","FYPO:0001985","FYPO:0001320","FYPO:0000631","FYPO:0002403"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, abnormal septum morphology, enlarged nucleus","synonyms":[{"name":"inviable after spore germination, undivided cell, abnormal septum morphology, enlarged nucleus","type":"exact"},{"name":"inviable after spore germination, without cell division, abnormal septum formation, enlarged nucleus","type":"exact"},{"name":"inviable following spore germination, without cell division, abnormal septum morphology, enlarged nucleus","type":"exact"},{"name":"inviable germinated spore, without cell division, abnormal septum morphology, enlarged nucleus","type":"exact"},{"name":"lethal after spore germination, without cell division, abnormal septum morphology, enlarged nucleus","type":"exact"}],"termid":"FYPO:0004115"}


id: SO:0001075
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Polypeptide region present in the lipid bilayer.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_structural_region","termid":"SO:0001070"},{"relation_name":"part_of","term_name":"membrane_structure","termid":"SO:0001071"}],"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":"intramembrane_polypeptide_region","secondary_identifiers":["BS:00156"],"synonyms":[{"name":"intramembrane","type":"related"},{"name":"intramembrane polypeptide region","type":"exact"}],"termid":"SO:0001075"}


id: MONDO:0003884
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign adipose tissue neoplasm of the rectum.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colorectal lipoma","termid":"MONDO:0003885"},{"relation_name":"is_a","term_name":"benign neoplasm of rectum","termid":"MONDO:0021462"}],"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":"lipoma of the rectum","secondary_identifiers":["UMLS:C1335684","MEDGEN:233392","DOID:6459","NCIT:C5551"],"synonyms":[{"name":"lipoma of rectum","type":"exact"},{"name":"rectal lipoma","type":"exact"},{"name":"rectum lipoma","type":"exact"}],"termid":"MONDO:0003884","xrefs":{"Monarch":{"xref_id":"0003884"}}}


id: PBO:0061517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSA2 pseudogene 7","termid":"PBO:0061517"}


id: PBO:0013836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choline transmembrane transporter family protein Ctl1","termid":"PBO:0013836"}


id: GO:0102618
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oryzalexin D + NAD(P) = oryzalexin B + H+ + NAD(P)H.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oryzalexin B synthase activity (obsolete GO:0102618)","termid":"GO:0102618"}


id: GO:0010872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of cholesterol esterification. Cholesterol esterification is the lipid modification process in which a sterol ester is formed by the combination of a carboxylic acid (often a fatty acid) and cholesterol. In the blood this process is associated with the conversion of free cholesterol into cholesteryl ester, which is then sequestered into the core of a lipoprotein particle.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cholesterol esterification (obsolete GO:0010872)","termid":"GO:0010872"}


id: PR:Q9URY6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A sodium-coupled monocarboxylate transporter 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02284","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":"urea active transporter 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC869.03c","secondary_identifiers":["UniProtKB:Q9URY6"],"synonyms":[{"name":"Spom972h-SLC5A8","type":"exact"}],"termid":"PR:Q9URY6"}


id: PR:P78813
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ent3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P78813"],"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":"ENTH domain-containing protein C794.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC794.11c","synonyms":[{"name":"Spom972h-ent3","type":"exact"}],"termid":"PR:P78813"}


id: PBO:0050291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HNF4A antisense RNA 1","termid":"PBO:0050291"}


id: MONDO:0001634
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well-circumscribed benign smooth muscle neoplasm arising from the bladder. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C6178"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bladder benign neoplasm","termid":"MONDO:0000384"},{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bladder leiomyoma","secondary_identifiers":["DOID:13109","UMLS:C1332560","MEDGEN:272371"],"synonyms":[{"name":"bladder leiomyoma","type":"exact"},{"name":"leiomyoma of bladder","type":"exact"},{"name":"leiomyoma of the bladder","type":"exact"},{"name":"leiomyoma of the urinary bladder","type":"exact"},{"name":"leiomyoma of urinary bladder","type":"exact"},{"name":"urinary bladder leiomyoma","type":"exact"}],"termid":"MONDO:0001634","xrefs":{"Monarch":{"xref_id":"0001634"}}}


id: PBO:0052077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"katanin regulatory subunit B1 like 1 pseudogene 2","termid":"PBO:0052077"}


id: PBO:0060371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myozenin 1","termid":"PBO:0060371"}


id: PBO:0030818
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_glucose_import","termid":"PBO:0030818"}


id: FYPO:0007139
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the medial cortical nodes is abolished during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to medial cortical node","termid":"FYPO:0003919"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to medial cortical node during mitotic interphase","synonyms":[{"name":"abolished protein localisation to medial cortical node during mitotic interphase","type":"exact"},{"name":"abolished protein localization to cortical medial dot during mitotic interphase","type":"exact"},{"name":"abolished protein localization to cytokinetic nodes during mitotic interphase","type":"related"},{"name":"abolished protein localization to medial cortical node during interphase during vegetative growth","type":"exact"},{"name":"abolished protein localization to medial cortical node during interphase of mitotic cell cycle","type":"exact"},{"name":"abolished protein localization to medial cortical nodes during mitotic interphase","type":"exact"},{"name":"abolished protein recruitment to medial cortical node during mitotic interphase","type":"related"},{"name":"protein localization to medial cortical node abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0007139"}


id: GO:0033108
data:
  {"annotated_genes":["SJAG_00703","SJAG_06135","SJAG_02979","SJAG_04116","SJAG_00852","SJAG_01996","SJAG_07008","SJAG_03337","SJAG_02229","SJAG_06468","SJAG_01838","SJAG_03099","SJAG_03322","SJAG_03046","SJAG_01140","SJAG_01895","SJAG_03574","SJAG_04450","SJAG_05199","SJAG_04553","SJAG_07005","SJAG_03873","SJAG_06392","SJAG_04899","SJAG_06046","SJAG_01405","SJAG_04603","SJAG_00449","SJAG_03296","SJAG_02480","SJAG_05302","SJAG_01141","SJAG_05305","SJAG_04560","SJAG_01503","SJAG_03399","SJAG_04348","SJAG_05398","SJAG_02975"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72362,89369,104334,107486,97681,107180,77090,117352,94993,62066,59004,60733,70620,89564,91993,102015,104079,72894,95008,107799,118648,78902,75971,92826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033617"},{"annotations":[74491,110453,89385,78451,110033,73850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033615"},{"annotations":[95009,102878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097250"},{"annotations":[99575,71123,67510,107803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034553"},{"annotations":[78643,107908,113157,60595,77200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034551"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a mitochondrial respiratory chain complex or between respiratory chain complexes to form high-order structures.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"mitochondrion organization","termid":"GO:0007005"}],"gene_count":39,"genes_by_uniquename":{"SJAG_00449":null,"SJAG_00703":null,"SJAG_00852":null,"SJAG_01140":null,"SJAG_01141":null,"SJAG_01405":null,"SJAG_01503":null,"SJAG_01838":null,"SJAG_01895":null,"SJAG_01996":null,"SJAG_02229":null,"SJAG_02480":null,"SJAG_02975":null,"SJAG_02979":null,"SJAG_03046":null,"SJAG_03099":null,"SJAG_03296":null,"SJAG_03322":null,"SJAG_03337":null,"SJAG_03399":null,"SJAG_03574":null,"SJAG_03873":null,"SJAG_04116":null,"SJAG_04348":null,"SJAG_04450":null,"SJAG_04553":null,"SJAG_04560":null,"SJAG_04603":null,"SJAG_04899":null,"SJAG_05199":null,"SJAG_05302":null,"SJAG_05305":null,"SJAG_05398":null,"SJAG_06046":null,"SJAG_06135":null,"SJAG_06392":null,"SJAG_06468":null,"SJAG_07005":null,"SJAG_07008":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0007005"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150","GO:0007005"],"is_obsolete":false,"name":"mitochondrial respiratory chain complex assembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0033108","terms_by_termid":{"GO:0033615":null,"GO:0033617":null,"GO:0034551":null,"GO:0034553":null,"GO:0097250":null}}


id: PBO:0070079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 36, pseudogene","termid":"PBO:0070079"}


id: GO:0097440
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A dendrite that emerges near the apical pole of a neuron. In bipolar neurons, apical dendrites are located on the opposite side of the soma from the axon.","definition_xrefs":["NIF_Subcellular:sao273773228"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite","termid":"GO:0030425"}],"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":"apical dendrite","termid":"GO:0097440"}


id: PBO:0040543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B3GAT1 divergent transcript","termid":"PBO:0040543"}


id: MONDO:0018344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete periodic paralysis with transient compartment-like syndrome (obsolete MONDO:0018344)","secondary_identifiers":["Orphanet:397755"],"termid":"MONDO:0018344","xrefs":{"Monarch":{"xref_id":"0018344"}}}


id: PBO:0029629
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-lagging_meiotic_chromosomes","termid":"PBO:0029629"}


id: GO:1902599
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of sulfathiazole across a membrane.","definition_xrefs":["GO_REF:0000069","GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide transport","termid":"GO:0042886"},{"relation_name":"is_a","term_name":"azole transmembrane transport","termid":"GO:0045117"},{"relation_name":"is_a","term_name":"sulfur compound transport","termid":"GO:0072348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"sulfathiazole transmembrane transport","secondary_identifiers":["GO:0015906"],"synonyms":[{"name":"sulfathiazole transport","type":"broad"},{"name":"sulphathiazole transport","type":"broad"}],"termid":"GO:1902599"}


id: PBO:0038493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily C member 4","termid":"PBO:0038493"}


id: MOD:00285
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct between an aspartic acid residue, a glutamic acid residue, a methionine residue (forming a sulfonium ether), and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron.","definition_xrefs":["PubMed:1320128","PubMed:10480885","RESID:AA0280","PubMed:10447690","PubMed:7840679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin modified residue","termid":"MOD:00699"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-aspartic acid residue","termid":"MOD:02066"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-glutamic acid residue","termid":"MOD:02068"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-methionine residue","termid":"MOD:02071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydroxyheme-L-aspartate ester-L-glutamate ester-L-methionine sulfonium","synonyms":[{"name":"1,5-bishydroxymethyl protoporphyrin IX 1-glutamate ester 5-aspartate ester 2-methionine sulfonium","type":"exact"},{"name":"BINDING Heme (covalent; via 3 links)","type":"exact"},{"name":"[13-[(S)-(4-amino-4-carboxy)butanoyloxymethyl]-3-[(S)-(3-amino-3-carboxy)propanoyloxymethyl]-12-[(S)-(3-amino-3-carboxy)propylsulfoniumethyl]-7-ethenyl-8,17-dimethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate","type":"exact"},{"name":"dihydroxyheme-L-aspartate ester-L-glutamate ester-L-methionine sulfonium","type":"exact"},{"name":"myeloperoxidase heme cofactor","type":"exact"}],"termid":"MOD:00285"}


id: PBO:0078294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRD antisense RNA 1","termid":"PBO:0078294"}


id: PBO:0076628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TANK binding kinase 1","termid":"PBO:0076628"}


id: GO:0075253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of uredospore formation, a process in which an asexual, dikaryotic, often rusty-colored spore, is formed in a structure called a uredinium.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043945"},{"relation_name":"is_a","term_name":"regulation of uredospore formation","termid":"GO:0075252"},{"relation_name":"positively_regulates","term_name":"uredospore formation","termid":"GO:0075251"}],"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 uredospore formation","synonyms":[{"name":"positive regulation of ureidospore formation","type":"exact"}],"termid":"GO:0075253"}


id: GO:0002331
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Expression of a single heavy chain allele during pre-B cell differentiation.","definition_xrefs":["GOC:add","GOC:jal","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gene expression","termid":"GO:0010468"},{"relation_name":"part_of","term_name":"pre-B cell differentiation","termid":"GO:0002329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"pre-B cell allelic exclusion","synonyms":[{"name":"pre-B lymphocyte allelic exclusion","type":"exact"}],"termid":"GO:0002331"}


id: PBO:0083793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential protein of the mitochondrial intermembrane space; forms a complex with Tim10p (TIM10 complex) that delivers hydrophobic proteins to the TIM22 complex for insertion into the inner membrane","termid":"PBO:0083793"}


id: GO:0015393
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 uracil/uridine permease activity (obsolete GO:0015393)","synonyms":[{"name":"uracil/uridine permease activity","type":"exact"}],"termid":"GO:0015393"}


id: GO:0018444
data:
  {"annotated_genes":["SJAG_01696","SJAG_00338"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72819,74170],"is_not":false,"summary":null,"term":"GO:0018444"}]},"cv_name":"cellular_component","definition":"A heterodimeric complex involved in the release of a nascent polypeptide chain from a ribosome.","definition_xrefs":["ISBN:0198547684"],"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":2,"genes_by_uniquename":{"SJAG_00338":null,"SJAG_01696":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"translation release factor complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"eukaryotic peptide chain release factor","type":"exact"},{"name":"peptide chain release factor","type":"broad"}],"termid":"GO:0018444","terms_by_termid":{"GO:0018444":null}}


id: GO:1902021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of bacterial-type flagellum-dependent cell motility.","definition_xrefs":["GOC:jl","GOC:cilia","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell motility","termid":"GO:2000145"},{"relation_name":"regulates","term_name":"bacterial-type flagellum-dependent cell motility","termid":"GO:0071973"}],"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 bacterial-type flagellum-dependent cell motility","synonyms":[{"name":"regulation of bacterial-type flagellar cell motility","type":"related"},{"name":"regulation of bacterial-type flagellum cell motility","type":"exact"},{"name":"regulation of flagellin-based flagellar cell motility","type":"exact"}],"termid":"GO:1902021"}


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


id: GO:1900292
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of galactotriose transport.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"regulation of galactotriose transport","termid":"GO:1900291"},{"relation_name":"negatively_regulates","term_name":"galactotriose transport","termid":"GO:2001093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of galactotriose transport","synonyms":[{"name":"down regulation of galactotriose transport","type":"exact"},{"name":"down-regulation of galactotriose transport","type":"exact"},{"name":"downregulation of galactotriose transport","type":"exact"},{"name":"inhibition of galactotriose transport","type":"narrow"}],"termid":"GO:1900292"}


id: GO:1904902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form an ESCRT III complex.","definition_xrefs":["GO_REF:0000079","GOC:pad","PMID:20588296","GOC:TermGenie","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ESCRT complex assembly","termid":"GO:1904895"}],"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:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"ESCRT III complex assembly","synonyms":[{"name":"ESCRT III complex formation","type":"exact"}],"termid":"GO:1904902"}


id: PBO:0002212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L10","termid":"PBO:0002212"}


id: PBO:0077378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 120A","termid":"PBO:0077378"}


id: PBO:0047454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCH and double SH3 domains 1","termid":"PBO:0047454"}


id: GO:0043915
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + L-seryl-tRNA(Sec) = ADP + O-phospho-L-seryl-tRNA(Sec).","definition_xrefs":["PMID:16201757","RHEA:25037","GOC:jl"],"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"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0140101","GO:0016301","GO:0016740","GO:0003824","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"L-seryl-tRNA(Sec) kinase activity","secondary_identifiers":["MetaCyc:RXN-10038","EC:2.7.1.164"],"synonyms":[{"name":"O-phosphoseryl-tRNA(Sec) kinase activity","type":"exact"}],"termid":"GO:0043915"}


id: MONDO:0013979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the LRRC6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 19","secondary_identifiers":["UMLS:C3543826","DOID:0110608","GARD:15883","MEDGEN:762332","OMIM:614935"],"synonyms":[{"name":"CILD19","type":"exact"},{"name":"LRRC6 primary ciliary dyskinesia","type":"exact"},{"name":"ciliary dyskinesia, primary, 19","type":"related"},{"name":"ciliary dyskinesia, primary, 19, with or without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 19","type":"exact"},{"name":"primary ciliary dyskinesia 19","type":"exact"},{"name":"primary ciliary dyskinesia 19 with or without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in LRRC6","type":"exact"},{"name":"primary ciliary dyskinesia type 19","type":"exact"}],"termid":"MONDO:0013979","xrefs":{"Monarch":{"xref_id":"0013979"}}}


id: GO:0006337
data:
  {"annotated_genes":["SJAG_01653","SJAG_04038","SJAG_02314"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90406,97416,117201],"is_not":false,"summary":null,"term":"GO:0006337"}]},"cv_name":"biological_process","definition":"The controlled breakdown of nucleosomes, the beadlike structural units of eukaryotic chromatin composed of histones and DNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex disassembly","termid":"GO:0032986"},{"relation_name":"is_a","term_name":"nucleosome organization","termid":"GO:0034728"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01653":null,"SJAG_02314":null,"SJAG_04038":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006325","GO:0008150"],"is_obsolete":false,"name":"nucleosome disassembly","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0006337","terms_by_termid":{"GO:0006337":null}}


id: PBO:0029812
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_actin_cable_organization_during_mitosis","termid":"PBO:0029812"}


id: PR:P79083
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A eukaryotic translation initiation factor 3 subunit I that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02224","PRO:DNx","PANTHER:PTHR19877:SF1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit I (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.05","secondary_identifiers":["UniProtKB:P79083"],"synonyms":[{"name":"Spom972h-EIF3I","type":"exact"},{"name":"eIF-3 39 kDa subunit homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eIF3 p39 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eIF3i (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eukaryotic translation initiation factor 3 39 kDa subunit homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"suppressor of uncontrolled mitosis 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P79083"}


id: PBO:0002376
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ageing","termid":"PBO:0002376"}


id: PBO:0053075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LBX1 antisense RNA 1","termid":"PBO:0053075"}


id: PBO:0117015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1191 antisense RNA 1","termid":"PBO:0117015"}


id: PBO:0052241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel tetramerization domain containing 11","termid":"PBO:0052241"}


id: PBO:0058889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 10526","termid":"PBO:0058889"}


id: GO:0097739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate of ferrichrome biosynthetic process in response to an iron stimulus.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of ferrichrome biosynthetic process","termid":"GO:1905569"},{"relation_name":"part_of","term_name":"cellular response to iron ion","termid":"GO:0071281"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"negatively_regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"negative regulation of ferrichrome biosynthetic process in response to iron","termid":"GO:0097739"}


id: PR:Q10341
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cys2 gene.","definition_xrefs":["UniProtKB:Q10341","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":"serine-O-acetyltransferase cys2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC106.17c","synonyms":[{"name":"Spom972h-cys2","type":"exact"}],"termid":"PR:Q10341"}


id: MONDO:0014868
data:
  {"annotated_genes":["SJAG_00261"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86442],"is_not":false,"summary":null,"term":"MONDO:0014868"}]},"cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the ARV1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 38","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16175","DOID:0080417","OMIM:617020","UMLS:C4310762","MEDGEN:934729"],"synonyms":[{"name":"ARV1 early infantile epileptic encephalopathy","type":"exact"},{"name":"DEE38","type":"exact"},{"name":"EIEE38","type":"exact"},{"name":"developmental and epileptic encephalopathy 38","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in ARV1","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 38","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 38; EIEE38","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 38","type":"exact"}],"termid":"MONDO:0014868","terms_by_termid":{"MONDO:0014868":null},"xrefs":{"Monarch":{"xref_id":"0014868"}}}


id: PBO:0084043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI lipid remodelase; responsible for introducing ceramides into GPI anchors having a C26:0 fatty acid in sn-2 of the glycerol moiety; can also use lyso-GPI protein anchors and various base resistant lipids as substrates; contains 14-16 transmembrane segments and several putative glycosylation and phosphorylation sites; null mutation is synthetically lethal with pkc1 deletion","termid":"PBO:0084043"}


id: PBO:0080260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 23 pseudogene","termid":"PBO:0080260"}


id: PBO:0089290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"But2 family protein But2, similar to cell surface molecules","termid":"PBO:0089290"}


id: PBO:0074137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 35 member A2","termid":"PBO:0074137"}


id: MONDO:0013580
data:
  {"annotated_genes":["SJAG_03064"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86278],"is_not":false,"summary":null,"term":"MONDO:0013580"}]},"cv_name":"mondo","definition":"Pyruvate dehydrogenase E1-beta deficiency is an extremely rare form of pyruvate dehydrogenase deficiency (PDHD) characterized by severe lactic acidosis, developmental delay and hypotonia.","definition_xrefs":["Orphanet:255138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate dehydrogenase deficiency","termid":"MONDO:0019169"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03064":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005244","MONDO:0004069","MONDO:0037792"],"is_obsolete":false,"name":"pyruvate dehydrogenase E1-beta deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3279841","GARD:17236","MESH:C566729","OMIM:614111","MEDGEN:481471"],"synonyms":[{"name":"PDHBD","type":"exact"},{"name":"pyruvate dehydrogenase E1-BETA deficiency","type":"related"},{"name":"pyruvate dehydrogenase E1-beta deficiency","type":"exact"},{"name":"pyruvate dehydrogenase complex E1 component subunit beta deficiency","type":"exact"}],"termid":"MONDO:0013580","terms_by_termid":{"MONDO:0013580":null},"xrefs":{"Monarch":{"xref_id":"0013580"}}}


id: PBO:0046956
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 78 member A","termid":"PBO:0046956"}


id: MONDO:1010730
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any severe combined immunodeficiency disease in golden hamsters in which the cause of the disease is a mutation in the IL2RG gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"severe combined immunodeficiency disease, non-human animal","termid":"MONDO:1011422"},{"relation_name":"is_a","term_name":"X-linked disease, non-human animal","termid":"MONDO:1012575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked severe combined immunodeficiency disease, IL2RG-related, golden hamster","secondary_identifiers":["OMIA:000899-10036"],"termid":"MONDO:1010730","xrefs":{"Monarch":{"xref_id":"1010730"}}}


id: PBO:0088965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi mannan polymerase I complex subunit Mnn9","termid":"PBO:0088965"}


id: MONDO:0009241
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fountain syndrome is an extremely rare multi-systemic genetic disorder characterized by intellectual disability, deafness, skeletal abnormalities and coarse facial features.","definition_xrefs":["Orphanet:3219"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fountain syndrome","secondary_identifiers":["GARD:64","OMIM:229120","MEDGEN:208650","MESH:C537270","SCTID:720957007","UMLS:C0795944"],"synonyms":[{"name":"deafness, skeletal dysplasia, lip granuloma","type":"related"},{"name":"deafness-skeletal dysplasia-coarse face with full lips syndrome","type":"exact"},{"name":"deafness-skeletal dysplasia-lip granuloma syndrome","type":"exact"},{"name":"fountain syndrome","type":"exact"},{"name":"intellectual disability, deafness, skeletal abnormalities, coarse face with full lips","type":"related"},{"name":"intellectual disability, sensorineural deafness, skeletal abnormalities, and coarse face with full lips","type":"related"},{"name":"mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips","type":"related"}],"termid":"MONDO:0009241","xrefs":{"Monarch":{"xref_id":"0009241"}}}


id: PBO:0030633
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_7-methylguanosine_cap_hypermethylation","termid":"PBO:0030633"}


id: MONDO:0850129
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A gastrointestinal system cancer that is located in the proximal esophagus and the distal stomach.","definition_xrefs":["DOID:0080374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"gastroesophageal cancer","secondary_identifiers":["MEDGEN:577508","UMLS:C0346619"],"termid":"MONDO:0850129","xrefs":{"Monarch":{"xref_id":"0850129"}}}


id: MONDO:0010603
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemophilia A","termid":"MONDO:0010602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"hemophilia A with vascular abnormality","secondary_identifiers":["OMIM:306800","MEDGEN:336105","MESH:C564415","UMLS:C1844137"],"synonyms":[{"name":"hemophilia A with vascular abnormality","type":"exact"}],"termid":"MONDO:0010603","xrefs":{"Monarch":{"xref_id":"0010603"}}}


id: MONDO:0017216
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Calciphylaxis cutis is a life-threatening syndrome characterized by progressive and painful skin ulcerations associated with media calcification of medium-size and small cutaneous arterial vessels. It affects mainly patients on dialysis or after renal transplantation.","definition_xrefs":["Orphanet:280065"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calciphylaxis","termid":"MONDO:0017215"},{"relation_name":"is_a","term_name":"skin vascular disease","termid":"MONDO:0019293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"calciphylaxis cutis","secondary_identifiers":["UMLS:C4274083","MEDGEN:900547","SCTID:717043006","GARD:21070"],"termid":"MONDO:0017216","xrefs":{"Monarch":{"xref_id":"0017216"}}}


id: PBO:0051763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"importin 7 pseudogene 2","termid":"PBO:0051763"}


id: PBO:0000939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHCH domain","termid":"PBO:0000939"}


id: FYPO:0007799
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a protein that is not normally found at the cell surface is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized protein during vegetative growth","termid":"FYPO:0000782"}],"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:0000138"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"protein mislocalized to cell surface during vegetative growth","synonyms":[{"name":"ectopic protein localization to cell surface during vegetative growth","type":"exact"},{"name":"protein mislocalised to cell surface during vegetative growth","type":"exact"},{"name":"protein mislocalized to cell surface during mitotic cell cycle","type":"related"}],"termid":"FYPO:0007799"}


id: GO:0019632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving shikimate, (3R,4S,5R)--3,4,5-trihydroxycyclohex-1-ene-1-carboxylate, the anion of shikimic acid. It is an important intermediate in the biosynthesis of aromatic amino acids.","definition_xrefs":["ISBN:0198547684","GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"shikimate metabolic process","synonyms":[{"name":"shikimate metabolism","type":"exact"}],"termid":"GO:0019632"}


id: SO:0001991
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A consensus AFLP fragment is an AFLP sequence produced from any alignment algorithm which uses assembled multiple AFLP sequences as input.","definition_xrefs":["GMOD:ea"],"direct_ancestors":[{"relation_name":"is_a","term_name":"consensus_region","termid":"SO:0000994"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"consensus_AFLP_fragment","synonyms":[{"name":"consensus AFLP fragment","type":"exact"},{"name":"consensus amplified fragment length polymorphism fragment","type":"exact"}],"termid":"SO:0001991"}


id: GO:0042116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change in morphology and behavior of a macrophage resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor.","definition_xrefs":["GOC:mgi_curators","ISBN:0781735149","PMID:14506301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukocyte activation","termid":"GO:0002274"}],"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":"macrophage activation","synonyms":[{"name":"macrophage polarization","type":"exact"}],"termid":"GO:0042116"}


id: MONDO:0007651
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"}],"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":"gastrocutaneous syndrome","secondary_identifiers":["MEDGEN:338154","OMIM:137270","icd11.foundation:1431211717","GARD:2438","MESH:C535651","Orphanet:2069","UMLS:C1850899"],"synonyms":[{"name":"gastrocutaneous syndrome","type":"exact"},{"name":"peptic Ulcer/hiatal hernia, multiple lentigines/cafe-Au-lait Spots, hypertelorism, myopia","type":"related"}],"termid":"MONDO:0007651","xrefs":{"Monarch":{"xref_id":"0007651"}}}


id: GO:0035746
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of granzyme A due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"production of molecular mediator of immune response","termid":"GO:0002440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"granzyme A production","termid":"GO:0035746"}


id: PBO:0002072
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.4.1.15","termid":"PBO:0002072"}


id: PBO:0031042
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cytoskeleton_organization","termid":"PBO:0031042"}


id: PBO:0117094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PSD3 antisense RNA 1","termid":"PBO:0117094"}


id: PBO:0049096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 153","termid":"PBO:0049096"}


id: GO:1904110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of plus-end directed microfilament motor activity.","definition_xrefs":["GOC:TermGenie","GOC:kmv","PMID:25717181","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of plus-end directed microfilament motor activity (obsolete GO:1904110)","synonyms":[{"name":"regulation of barbed-end directed actin-filament motor activity","type":"exact"},{"name":"regulation of plus-end directed actin filament motor activity","type":"related"},{"name":"regulation of plus-end directed actin-filament motor activity","type":"exact"}],"termid":"GO:1904110"}


id: PBO:0011071
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in eukaryotes only","termid":"PBO:0011071"}


id: GO:0000341
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to the trimethylguanosine (m(3)(2,2,7)-GTP) group located at the 5' end of some RNA molecules. Such trimethylated cap structures, generally produced by posttranscriptional modification of a 7-methylguanosine cap, are often found on snRNAs and snoRNAs transcribed by RNA polymerase II, but have also be found on snRNAs transcribed by RNA polymerase III. They have also been found on a subset of the mRNA population in some species, e.g. C. elegans.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA cap binding","termid":"GO:0000339"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003723","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"RNA trimethylguanosine cap binding","synonyms":[{"name":"RNA m2,2,7G cap binding","type":"exact"}],"termid":"GO:0000341"}


id: GO:0007236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of Ssk1 protein (obsolete GO:0007236)","synonyms":[{"name":"activation of Ssk1 protein","type":"exact"}],"termid":"GO:0007236"}


id: GO:0010983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of high-density lipoprotein particle clearance. High-density lipoprotein particle clearance is the process in which a high-density lipoprotein particle is removed from the blood via receptor-mediated endocytosis and its constituent parts degraded.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of high-density lipoprotein particle clearance","termid":"GO:0010982"},{"relation_name":"is_a","term_name":"positive regulation of lipoprotein particle clearance","termid":"GO:0010986"},{"relation_name":"positively_regulates","term_name":"high-density lipoprotein particle clearance","termid":"GO:0034384"}],"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 high-density lipoprotein particle clearance","termid":"GO:0010983"}


id: PBO:0080131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VANGL planar cell polarity protein 1","termid":"PBO:0080131"}


id: MONDO:0011312
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial papillary or follicular thyroid carcinoma","termid":"MONDO:0017895"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"thyroid carcinoma, nonmedullary, with or without cell oxyphilia","secondary_identifiers":["UMLS:C1863925","GARD:15354","OMIM:603386","MEDGEN:400409","MESH:C537842"],"synonyms":[{"name":"TCO","type":"related"},{"name":"TCO 1","type":"related"},{"name":"TCO1","type":"related"},{"name":"nonmedullary thyroid carcinoma, with or without cell oxyphilia","type":"related"},{"name":"thyroid carcinoma, nonmedullary, with cell oxyphilia","type":"exact"},{"name":"thyroid carcinoma, nonmedullary, with or without cell oxyphilia","type":"exact"}],"termid":"MONDO:0011312","xrefs":{"Monarch":{"xref_id":"0011312"}}}


id: MONDO:0015280
data:
  {"annotated_genes":["SJAG_00993","SJAG_03453","SJAG_02342","SJAG_01181"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014112"},{"annotations":[85380,85381,85382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014113"},{"annotations":[85385,85386,85387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014114"}]},"cv_name":"mondo","definition":"Cardiofaciocutaneous (CFC) syndrome is a RASopathy characterized by craniofacial dysmorphology, congenital heart disease, dermatological abnormalities (most commonly hyperkeratotic skin and sparse, curly hair), growth retardation and intellectual disability.","definition_xrefs":["Orphanet:1340"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"Noonan syndrome and Noonan-related syndrome","termid":"MONDO:0020297"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00993":null,"SJAG_01181":null,"SJAG_02342":null,"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005093"],"is_obsolete":false,"name":"cardiofaciocutaneous syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NORD:891","OMIMPS:115150","DOID:0060233","NANDO:1200462","SCTID:403770008","NCIT:C84617","GARD:9146","UMLS:C1275081","NANDO:2200967","MESH:C535579","MEDGEN:266149"],"synonyms":[{"name":"CFC","type":"exact"},{"name":"CFC syndrome","type":"exact"},{"name":"cardio-facial-cutaneous syndrome","type":"exact"},{"name":"cardio-facio-cutaneous syndrome","type":"related"},{"name":"cardiofaciocutaneous (CFC) syndrome","type":"exact"},{"name":"cardiofaciocutaneous syndrome","type":"exact"},{"name":"congenital heart defects characteristic facial appearance ectodermal abnormalities and growth failure","type":"related"}],"termid":"MONDO:0015280","terms_by_termid":{"MONDO:0014112":null,"MONDO:0014113":null,"MONDO:0014114":null},"xrefs":{"Monarch":{"xref_id":"0015280"}}}


id: GO:1903042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of chondrocyte hypertrophy.","definition_xrefs":["PMID:23928032","GO_REF:0000058","GOC:TermGenie","GOC:mr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell growth","termid":"GO:0030308"},{"relation_name":"is_a","term_name":"negative regulation of developmental growth","termid":"GO:0048640"},{"relation_name":"is_a","term_name":"negative regulation of chondrocyte development","termid":"GO:0061182"},{"relation_name":"is_a","term_name":"regulation of chondrocyte hypertrophy","termid":"GO:1903041"},{"relation_name":"negatively_regulates","term_name":"chondrocyte hypertrophy","termid":"GO:0003415"}],"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 chondrocyte hypertrophy","synonyms":[{"name":"down regulation of chondrocyte hypertrophy","type":"exact"},{"name":"down-regulation of chondrocyte hypertrophy","type":"exact"},{"name":"downregulation of chondrocyte hypertrophy","type":"exact"},{"name":"inhibition of chondrocyte hypertrophy","type":"narrow"}],"termid":"GO:1903042"}


id: FYPO:0004143
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 nitrite (NO2-) ions measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular nitrite level","synonyms":[{"name":"increased cellular nitrite accumulation","type":"related"},{"name":"increased cellular nitrite ion level","type":"exact"},{"name":"increased cellular nitrite level during mitotic cell cycle","type":"related"},{"name":"increased cellular nitrite level during vegetative growth","type":"exact"}],"termid":"FYPO:0004143"}


id: MONDO:0859215
data:
  {"annotated_genes":["SJAG_MIT09"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86443],"is_not":false,"summary":null,"term":"MONDO:0859215"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_MIT09":null},"genotype_count":0,"is_obsolete":false,"name":"dystonia, early-onset, and/or spastic paraplegia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1794261","UMLS:C5562051","OMIM:619681","DOID:0070445"],"termid":"MONDO:0859215","terms_by_termid":{"MONDO:0859215":null},"xrefs":{"Monarch":{"xref_id":"0859215"}}}


id: GO:0015954
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways by which a pyrimidine ribonucleotide is synthesized from another pyrimidine ribonucleotide.","definition_xrefs":["GOC:mah","ISBN:0306444747","ISBN:0471394831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide metabolic process","termid":"GO:0009218"},{"relation_name":"is_a","term_name":"pyrimidine nucleotide interconversion","termid":"GO:0015953"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"pyrimidine ribonucleotide interconversion","termid":"GO:0015954"}


id: PBO:0072001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S7 pseudogene 3","termid":"PBO:0072001"}


id: PBO:0090553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-K ortholog Sim4","termid":"PBO:0090553"}


id: PBO:0052618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KRI1 homolog","termid":"PBO:0052618"}


id: PBO:0087129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein; promotes elongation, regulates termination, and carries poly(A) mRNA from nucleus to cytoplasm; represses translation initiation by binding eIF4G; required for pre-mRNA splicing; interacts with E3 ubiquitin ligase Bre1p, linking histone ubiquitination to mRNA processing; may have role in telomere maintenance; dissociation from mRNAs promoted by Mtr10p; phosphorylated by Sky1p in cytoplasm; protein abundance increases in response to DNA replication stress","termid":"PBO:0087129"}


id: PBO:0078781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 6-1","termid":"PBO:0078781"}


id: MONDO:0012950
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intracranial berry aneurysm","termid":"MONDO:0016483"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aneurysm, intracranial berry, 10","secondary_identifiers":["OMIM:612587","MEDGEN:390811","DOID:0080973","GARD:18328","MESH:C567237","UMLS:C2675484"],"synonyms":[{"name":"ANIB10","type":"exact"},{"name":"aneurysm, intracranial BERRY, 10","type":"related"}],"termid":"MONDO:0012950","xrefs":{"Monarch":{"xref_id":"0012950"}}}


id: GO:0046016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involving glucose that activates or increases the rate of transcription.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon catabolite activation of transcription","termid":"GO:0045991"},{"relation_name":"is_a","term_name":"regulation of transcription by glucose","termid":"GO:0046015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"positively_regulates","termid":"GO:0006351"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006355"}],"interesting_parent_ids":["GO:0006351","GO:0008150","GO:0010467","GO:0006355"],"is_obsolete":false,"name":"positive regulation of transcription by glucose","synonyms":[{"name":"activation of transcription by glucose","type":"narrow"},{"name":"stimulation of transcription by glucose","type":"narrow"},{"name":"up regulation of transcription by glucose","type":"exact"},{"name":"up-regulation of transcription by glucose","type":"exact"},{"name":"upregulation of transcription by glucose","type":"exact"}],"termid":"GO:0046016"}


id: PBO:0068359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNF139 divergent transcript","termid":"PBO:0068359"}


id: GO:1903532
data:
  {"annotated_genes":["SJAG_00661"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045921"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of secretion by cell.","definition_xrefs":["GOC:pm","PMID:12130530","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of secretion","termid":"GO:0051047"},{"relation_name":"is_a","term_name":"regulation of secretion by cell","termid":"GO:1903530"},{"relation_name":"positively_regulates","term_name":"secretion by cell","termid":"GO:0032940"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00661":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of secretion by cell","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of cellular secretion","type":"narrow"},{"name":"activation of secretion by cell","type":"narrow"},{"name":"positive regulation of cellular secretion","type":"exact"},{"name":"up regulation of cellular secretion","type":"exact"},{"name":"up regulation of secretion by cell","type":"exact"},{"name":"up-regulation of cellular secretion","type":"exact"},{"name":"up-regulation of secretion by cell","type":"exact"},{"name":"upregulation of cellular secretion","type":"exact"},{"name":"upregulation of secretion by cell","type":"exact"}],"termid":"GO:1903532","terms_by_termid":{"GO:0045921":null}}


id: MONDO:0100018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pityriasis rubra pilaris that occurs around the fifth or sixth decade of life.","direct_ancestors":[{"relation_name":"is_a","term_name":"pityriasis rubra pilaris","termid":"MONDO:0100017"}],"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":"adult onset pityriasis rubra pilaris","synonyms":[{"name":"adult onset PRP","type":"exact"}],"termid":"MONDO:0100018","xrefs":{"Monarch":{"xref_id":"0100018"}}}


id: MONDO:0010565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Protanopia is a severe type of color vision deficiency caused by the complete absence of red retinal photoreceptors. Protans have difficulties distinguishing between blue and green colors and also between red and green colors. It is a form of dichromatism in which the subject can only perceive light wavelengths from 400 to 650 nm, instead of the usual 700 nm. Pure reds cannot be seen, instead appearing black; purple colors cannot be distinguished from blues; more orange-tinted reds may appear as very dim yellows, and all orange-yellow-green shades of too long a wavelength to stimulate the blue receptors appear as a similar yellow hue. It is hereditary, sex-linked, and present in 1% of males.","definition_xrefs":["EFO:0005580"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color vision disorder","termid":"MONDO:0001703"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"red color blindness","secondary_identifiers":["SCTID:51445007","ICD10CM:H53.54","UMLS:C0155015","Orphanet:319691","OMIM:303900","DOID:13910","ICD9:368.51","MEDGEN:56350"],"synonyms":[{"name":"CBP","type":"related"},{"name":"colorblindness, partial, protan series","type":"related"},{"name":"colorblindness, protan","type":"exact"},{"name":"partial achromatopsia, protan type","type":"exact"},{"name":"protan defect","type":"exact"},{"name":"protanomaly","type":"related"},{"name":"protanopia","type":"exact"},{"name":"red color blindness","type":"exact"},{"name":"red colorblindness","type":"related"}],"termid":"MONDO:0010565","xrefs":{"Monarch":{"xref_id":"0010565"}}}


id: GO:0072000
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of polysaccharides in the ascus wall that contributes to the release of ascospores from the ascus.","definition_xrefs":["GOC:mah","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete extracellular polysaccharide catabolic process involved in ascospore release from ascus (obsolete GO:0072000)","synonyms":[{"name":"ascus catabolic process","type":"related"},{"name":"ascus endolysis","type":"related"},{"name":"extracellular polysaccharide breakdown involved in ascospore release from ascus","type":"exact"},{"name":"extracellular polysaccharide catabolism involved in ascospore release from ascus","type":"exact"},{"name":"extracellular polysaccharide degradation involved in ascospore release from ascus","type":"exact"}],"termid":"GO:0072000"}


id: PBO:0072904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretory carrier membrane protein 2","termid":"PBO:0072904"}


id: PBO:0083697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Epsilon subunit of the F1 sector of mitochondrial F1F0 ATP synthase; which is a large, evolutionarily conserved enzyme complex required for ATP synthesis; F1 translationally regulates ATP6 and ATP8 expression to achieve a balanced output of ATP synthase genes encoded in nucleus and mitochondria; phosphorylated","termid":"PBO:0083697"}


id: MONDO:0016266
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that involves the body of uterus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"uterine carcinoma","termid":"MONDO:0005213"},{"relation_name":"is_a","term_name":"uterine corpus cancer","termid":"MONDO:0006003"}],"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":"squamous cell carcinoma of the corpus uteri","secondary_identifiers":["UMLS:C4707099","GARD:20479","ICD10CM:C54.1","MEDGEN:1633992","Orphanet:213716"],"synonyms":[{"name":"body of uterus squamous cell carcinoma","type":"exact"},{"name":"endometrial squamous cell carcinoma","type":"related"}],"termid":"MONDO:0016266","xrefs":{"Monarch":{"xref_id":"0016266"}}}


id: GO:0005985
data:
  {"annotated_genes":["SJAG_04301"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77168],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005987"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving sucrose, the disaccharide fructofuranosyl-glucopyranoside.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disaccharide metabolic process","termid":"GO:0005984"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04301":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"sucrose metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"sucrose metabolism","type":"exact"}],"termid":"GO:0005985","terms_by_termid":{"GO:0005987":null}}


id: PBO:0050410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HNRNPD divergent transcript","termid":"PBO:0050410"}


id: MONDO:0020626
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete yt blood group antigen (obsolete MONDO:0020626)","secondary_identifiers":["OMIM:112100"],"synonyms":[{"name":"Cartwright Antigen","type":"related"},{"name":"YT BLOOD GROUP ANTIGEN","type":"related"},{"name":"blood group, Yt system","type":"exact"}],"termid":"MONDO:0020626","xrefs":{"Monarch":{"xref_id":"0020626"}}}


id: GO:0018555
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: phenanthrene + NADH + H+ + O2 = NAD+ + cis-3,4-dihydroxy-3,4-dihydrophenanthrene.","definition_xrefs":["UM-BBD_reactionID:r0455"],"gene_count":0,"genotype_count":0,"name":"obsolete phenanthrene dioxygenase activity (obsolete GO:0018555)","termid":"GO:0018555"}


id: GO:2000867
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of estrone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of steroid hormone secretion","termid":"GO:2000831"},{"relation_name":"regulates","term_name":"estrone secretion","termid":"GO:0035943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of estrone secretion","synonyms":[{"name":"regulation of 3-hydroxy-1,3,5(10)-estratrien-17-one secretion","type":"exact"},{"name":"regulation of folliculin secretion","type":"exact"}],"termid":"GO:2000867"}


id: GO:0048829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the root cap over time, from its formation to the mature structure. The root cap protects the root meristem from friction as the root grows through the soil. The cap is made up of a group of parenchyma cells which secrete a glycoprotein mucilage as a lubricant.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"root development","termid":"GO:0048364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"root cap development","termid":"GO:0048829"}


id: MONDO:0002955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A slow growing, locally infiltrating carcinoma that arises from the vulva. It is characterized by the presence of malignant cells that resemble the basal cells that are present in the epidermis.","definition_xrefs":["NCIT:C6381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"},{"relation_name":"is_a","term_name":"vulvar squamous cell carcinoma","termid":"MONDO:0024609"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"vulva basal cell carcinoma","secondary_identifiers":["Orphanet:494451","DOID:4301","icd11.foundation:247568702","GARD:22006","MEDGEN:234481","UMLS:C1336977","SCTID:717731002"],"synonyms":[{"name":"basal cell carcinoma of the vulva","type":"exact"},{"name":"basal cell carcinoma of vulva","type":"exact"},{"name":"mammalian vulva skin basal cell carcinoma","type":"exact"},{"name":"skin basal cell carcinoma of mammalian vulva","type":"exact"},{"name":"vulvar basal cell cancer","type":"exact"},{"name":"vulvar basal cell carcinoma","type":"exact"}],"termid":"MONDO:0002955","xrefs":{"Monarch":{"xref_id":"0002955"}}}


id: PBO:0113445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit beta1 of the nascent polypeptide-associated complex (NAC); involved in protein targeting to mitochondria; peripheral component of cytoplasmic ribosomes; regulates Atg32p phosphorylation to promote respiration-induced mitophagy; enhances DNA binding of the Gal4p; homolog of human BTF3b; EGD1 has a paralog, BTT1, that arose from the whole genome duplication","termid":"PBO:0113445"}


id: FYPO:0003257
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of proline into the cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased amino acid import during vegetative growth","termid":"FYPO:0001360"},{"relation_name":"is_a","term_name":"abnormal proline import","termid":"FYPO:0003256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased proline import","synonyms":[{"name":"decreased L-proline import","type":"exact"},{"name":"decreased L-proline import across plasma membrane","type":"exact"},{"name":"decreased proline import during mitotic cell cycle","type":"related"},{"name":"decreased proline import during vegetative growth","type":"exact"},{"name":"decreased proline import into cell","type":"exact"},{"name":"decreased proline uptake","type":"exact"},{"name":"reduced proline import","type":"exact"}],"termid":"FYPO:0003257"}


id: GO:0009184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of purine deoxyribonucleoside diphosphate, a compound consisting of a purine base linked to a deoxyribose sugar esterified with diphosphate on the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleoside diphosphate catabolic process","termid":"GO:0009137"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside diphosphate metabolic process","termid":"GO:0009182"},{"relation_name":"is_a","term_name":"deoxyribonucleoside diphosphate catabolic process","termid":"GO:0009192"}],"gene_count":0,"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:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"purine deoxyribonucleoside diphosphate catabolic process","synonyms":[{"name":"purine deoxyribonucleoside diphosphate breakdown","type":"exact"},{"name":"purine deoxyribonucleoside diphosphate catabolism","type":"exact"},{"name":"purine deoxyribonucleoside diphosphate degradation","type":"exact"}],"termid":"GO:0009184"}


id: PBO:0040525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"antizyme inhibitor 2","termid":"PBO:0040525"}


id: MONDO:0000653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the integumental system","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"}],"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":"integumentary system cancer","secondary_identifiers":["DOID:0060122"],"synonyms":[{"name":"cancer of integumental system","type":"exact"},{"name":"integumental system cancer","type":"exact"},{"name":"malignant integumental system neoplasm","type":"exact"},{"name":"malignant neoplasm of integumental system","type":"exact"}],"termid":"MONDO:0000653","xrefs":{"Monarch":{"xref_id":"0000653"}}}


id: RO:HOM0000055
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Paralogy that is characterized by duplication of adjacent sequences on a chromosome segment.","definition_xrefs":["ISBN:978-0878932665"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in_paralogy_relationship_with","termid":"RO:HOM0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_tandem_paralogy_relationship_with","synonyms":[{"name":"iterative paralogy","type":"related"},{"name":"serial paralogy","type":"related"},{"name":"tandem paralogous to","type":"exact"}],"termid":"RO:HOM0000055"}


id: GO:1901629
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of presynaptic membrane organization.","definition_xrefs":["GOC:TermGenie","PMID:22426000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synapse organization","termid":"GO:0050807"},{"relation_name":"regulates","term_name":"presynaptic membrane organization","termid":"GO:0097090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"regulation of presynaptic membrane organization","synonyms":[{"name":"regulation of pre-synaptic membrane organization","type":"exact"},{"name":"regulation of presynaptic membrane organisation","type":"exact"}],"termid":"GO:1901629"}


id: MONDO:0009371
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"3 hydroxyisobutyric aciduria is characterized by ketoacidotic episodes, cerebral anomalies and facial dysmorphism. It is an organic aciduria that involves valine metabolism. Thirteen cases have been described in the literature so far. Transmission is thought to be autosomal recessive.","definition_xrefs":["Orphanet:939"],"direct_ancestors":[{"relation_name":"is_a","term_name":"classic organic aciduria","termid":"MONDO:0019215"},{"relation_name":"is_a","term_name":"inborn disorder of branched-chain amino acid metabolism","termid":"MONDO:0019242"},{"relation_name":"is_a","term_name":"valine metabolism disease","termid":"MONDO:0037870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"3-hydroxyisobutyric aciduria","secondary_identifiers":["UMLS:C0342737","icd11.foundation:1293648631","MESH:C535312","SCTID:237957007","ICD9:791.9","MEDGEN:90996","OMIM:236795","GARD:5662"],"synonyms":[{"name":"3-hydroxyisobutyric aciduria","type":"exact"},{"name":"disorder of valine metabolism","type":"related"}],"termid":"MONDO:0009371","xrefs":{"Monarch":{"xref_id":"0009371"}}}


id: GO:0036381
data:
  {"annotated_genes":["SJAG_00283"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[63908],"is_not":false,"summary":null,"term":"GO:0036381"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribose 5-phosphate + D-glyceraldehyde 3-phosphate + L-glutamine = pyridoxal 5'-phosphate + L-glutamate + 3 H2O + phosphate. The reaction occurs in two steps: L-glutamine + H2O = L-glutamate + NH3, and subsequently D-ribose 5-phosphate + D-glyceraldehyde 3-phosphate + NH3 = pyridoxal 5'-phosphate + 4 H2O + phosphate.","definition_xrefs":["EC:4.3.3.6","GOC:rs"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amine-lyase activity","termid":"GO:0016843"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00283":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"pyridoxal 5'-phosphate synthase (glutamine hydrolysing) activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["RHEA:31507","KEGG_REACTION:R10089","MetaCyc:RXN-11322"],"synonyms":[{"name":"PdxST activity","type":"related"},{"name":"pyridoxal 5'-phosphate synthase (glutamine hydrolyzing) activity","type":"related"}],"termid":"GO:0036381","terms_by_termid":{"GO:0036381":null}}


id: GO:1902005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of proline biosynthetic process.","definition_xrefs":["GOC:TermGenie","PMID:23415322"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proline metabolic process","termid":"GO:2000214"},{"relation_name":"is_a","term_name":"regulation of amino acid biosynthetic process","termid":"GO:2000282"},{"relation_name":"regulates","term_name":"proline biosynthetic process","termid":"GO:0006561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"regulation of proline biosynthetic process","synonyms":[{"name":"regulation of proline anabolism","type":"exact"},{"name":"regulation of proline biosynthesis","type":"exact"},{"name":"regulation of proline formation","type":"exact"},{"name":"regulation of proline synthesis","type":"exact"}],"termid":"GO:1902005"}


id: PBO:0001976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNAP receptor, synaptobrevin family","termid":"PBO:0001976"}


id: PR:O74892
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 40S ribosomal protein S2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04937","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":"40S ribosomal protein S2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC576.08c","secondary_identifiers":["UniProtKB:O74892"],"synonyms":[{"name":"Spom972h-RPS2","type":"exact"}],"termid":"PR:O74892"}


id: GO:0017148
data:
  {"annotated_genes":["SJAG_00786","SJAG_00169","SJAG_02592","SJAG_03869","SJAG_05000","SJAG_03501","SJAG_02638","SJAG_00423","SJAG_02026","SJAG_01942","SJAG_00690","SJAG_04291"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99766,118528,115154,95922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000766"},{"annotations":[91648,112462],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904689"},{"annotations":[70305,94704,75585,109982,99660,115916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"},{"annotations":[75722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001125"},{"annotations":[99774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141014"}]},"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 proteins by the translation of mRNA or circRNA.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation","termid":"GO:0006417"},{"relation_name":"is_a","term_name":"negative regulation of gene expression","termid":"GO:0010629"},{"relation_name":"is_a","term_name":"negative regulation of protein metabolic process","termid":"GO:0051248"},{"relation_name":"negatively_regulates","term_name":"translation","termid":"GO:0006412"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00423":null,"SJAG_00690":null,"SJAG_00786":null,"SJAG_01942":null,"SJAG_02026":null,"SJAG_02592":null,"SJAG_02638":null,"SJAG_03501":null,"SJAG_03869":null,"SJAG_04291":null,"SJAG_05000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of translation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0016478"],"synonyms":[{"name":"down regulation of protein biosynthetic process","type":"exact"},{"name":"down-regulation of protein biosynthetic process","type":"exact"},{"name":"downregulation of protein biosynthetic process","type":"exact"},{"name":"inhibition of protein biosynthetic process","type":"narrow"},{"name":"negative regulation of protein anabolism","type":"exact"},{"name":"negative regulation of protein biosynthesis","type":"exact"},{"name":"negative regulation of protein biosynthetic process","type":"exact"},{"name":"negative regulation of protein formation","type":"exact"},{"name":"negative regulation of protein synthesis","type":"exact"},{"name":"protein biosynthesis inhibitor activity","type":"related"},{"name":"protein biosynthetic process inhibitor activity","type":"related"}],"termid":"GO:0017148","terms_by_termid":{"GO:0141014":null,"GO:1904689":null,"GO:1990625":null,"GO:2000766":null,"GO:2001125":null}}


id: PBO:0110268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase II complex subunit Rpb3","termid":"PBO:0110268"}


id: MONDO:0006935
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The obstruction of the right ventricular outflow tract that originates within the body of the right ventricle, that exists at the time of birth; it often occurs in association with other intracardiac anomalies.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary valve stenosis","termid":"MONDO:0006936"}],"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":"pulmonary subvalvular stenosis","secondary_identifiers":["NANDO:2100092","EFO:1001137","SCTID:204370002","UMLS:C0034084","DOID:8861","ICD9:746.83","MEDGEN:11030","MESH:D011662","NCIT:C34961","NANDO:2200276"],"synonyms":[{"name":"congenital infundibular stenosis","type":"exact"},{"name":"infundibular pulmonic stenosis","type":"exact"},{"name":"infundibular pulmonic stenosis, congenital","type":"exact"},{"name":"pulmonary infundibular stenosis","type":"exact"},{"name":"subvalvular pulmonic stenosis","type":"exact"}],"termid":"MONDO:0006935","xrefs":{"Monarch":{"xref_id":"0006935"}}}


id: PBO:0078798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 16-5","termid":"PBO:0078798"}


id: PR:O13782
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cpp1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13782"],"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 farnesyltransferase subunit beta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.04c","synonyms":[{"name":"CAAX farnesyltransferase subunit beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"FTase-beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-cpp1","type":"exact"},{"name":"ras proteins prenyltransferase subunit beta (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13782"}


id: PBO:0038893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADGB divergent transcript","termid":"PBO:0038893"}


id: PBO:0047504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fer-1 like family member 5","termid":"PBO:0047504"}


id: PBO:0071923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4 X-linked","termid":"PBO:0071923"}


id: GO:0072041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the occurrence or rate of mesenchymal stem cell death by apoptotic process that contributes to the shaping of the nephron.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal cell apoptotic process involved in nephron morphogenesis","termid":"GO:0072039"},{"relation_name":"is_a","term_name":"positive regulation of apoptotic process involved in morphogenesis","termid":"GO:1902339"},{"relation_name":"is_a","term_name":"positive regulation of somatic stem cell population maintenance","termid":"GO:1904674"},{"relation_name":"is_a","term_name":"positive regulation of mesenchymal cell apoptotic process","termid":"GO:2001055"},{"relation_name":"positively_regulates","term_name":"mesenchymal stem cell maintenance involved in nephron morphogenesis","termid":"GO:0072038"},{"relation_name":"positively_regulates","term_name":"mesenchymal cell apoptotic process involved in nephron morphogenesis","termid":"GO:1901145"}],"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 mesenchymal cell apoptotic process involved in nephron morphogenesis","synonyms":[{"name":"positive regulation of mesenchymal stem cell apoptosis involved in nephron morphogenesis","type":"narrow"},{"name":"positive regulation of mesenchymal stem cell apoptotic process involved in nephron morphogenesis","type":"exact"}],"termid":"GO:0072041"}


id: MONDO:1012527
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ichthyosis fetalis, non-human animal","termid":"MONDO:1011764"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ichthyosis fetalis, sheep","secondary_identifiers":["OMIA:002193-9940"],"termid":"MONDO:1012527","xrefs":{"Monarch":{"xref_id":"1012527"}}}


id: PBO:0091242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxylic acid transmembrane transporter","termid":"PBO:0091242"}


id: GO:0034182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the extent to which the association between sister chromatids of a replicated chromosome is maintained during a mitotic cell cycle.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of maintenance of sister chromatid cohesion","termid":"GO:0034091"},{"relation_name":"regulates","term_name":"maintenance of mitotic sister chromatid cohesion","termid":"GO:0034088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of maintenance of mitotic sister chromatid cohesion","termid":"GO:0034182"}


id: GO:0015743
data:
  {"annotated_genes":["SJAG_01406","SJAG_02140","SJAG_02011"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63954],"is_not":false,"summary":null,"term":"GO:0015743"},{"annotations":[101973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098714"},{"annotations":[67747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071423"}]},"cv_name":"biological_process","definition":"The directed movement of malate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C4-dicarboxylate transport","termid":"GO:0015740"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01406":null,"SJAG_02011":null,"SJAG_02140":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"malate transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial alpha-ketoglutarate/malate transport","type":"related"}],"termid":"GO:0015743","terms_by_termid":{"GO:0015743":null,"GO:0071423":null,"GO:0098714":null}}


id: MONDO:0000571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete CD3zeta deficiency (obsolete MONDO:0000571)","termid":"MONDO:0000571","xrefs":{"Monarch":{"xref_id":"0000571"}}}


id: PBO:0062201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily X member 1","termid":"PBO:0062201"}


id: GO:0046152
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving ommochromes, any of a large group of natural polycyclic pigments commonly found in the Arthropoda, particularly in the ommatidia of the compound eye.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye pigment metabolic process","termid":"GO:0042441"},{"relation_name":"is_a","term_name":"ocellus pigment metabolic process","termid":"GO:0046158"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"ommochrome metabolic process","synonyms":[{"name":"ommochrome metabolism","type":"exact"}],"termid":"GO:0046152"}


id: GO:0150147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of a cell-cell junction into its constituent components.","definition_xrefs":["PMID:25490267","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell junction organization","termid":"GO:0045216"},{"relation_name":"is_a","term_name":"cell junction disassembly","termid":"GO:0150146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell-cell junction disassembly","termid":"GO:0150147"}


id: PBO:0068836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 74, pseudogene","termid":"PBO:0068836"}


id: MONDO:0011877
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant osteopetrosis type I (ADO I) is a sclerosing bone disorder characterized by skeletal densification that predominantly involves the cranial vault.","definition_xrefs":["Orphanet:2783"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant osteopetrosis","termid":"MONDO:0020645"}],"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 osteopetrosis 1","secondary_identifiers":["MEDGEN:335932","MESH:C536056","DOID:0110937","UMLS:C1843330","OMIM:607634","GARD:4151"],"synonyms":[{"name":"LRP5 osteopetrosis (disease)","type":"exact"},{"name":"OPTA1","type":"exact"},{"name":"autosomal dominant osteopetrosis type 1","type":"exact"},{"name":"osteopetrosis (disease) caused by mutation in LRP5","type":"exact"},{"name":"osteopetrosis autosomal dominant type 1","type":"related"},{"name":"osteopetrosis, autosomal dominant 1","type":"related"},{"name":"osteopetrosis, autosomal dominant type 1","type":"exact"},{"name":"osteopetrosis, autosomal dominant, type 1","type":"related"}],"termid":"MONDO:0011877","xrefs":{"Monarch":{"xref_id":"0011877"}}}


id: GO:0000806
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The sex chromosome present in males of species in which the male is the heterogametic sex; generally, the sex chromosome that pairs with the X chromosome in the heterogametic sex. The Y chromosome is absent from the cells of females and present in one copy in the somatic cells of males.","definition_xrefs":["Wikipedia:XY_sex-determination_system","GOC:mr","PMID:20622855","GOC:mah","ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sex chromosome","termid":"GO:0000803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0005575"],"is_obsolete":false,"name":"Y chromosome","secondary_identifiers":["Wikipedia:Y_chromosome"],"termid":"GO:0000806"}


id: SO:0000478
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene including C-region (and introns if present) with 5' UTR (SO:0000204) and 3' UTR (SO:0000205).","direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_segment","termid":"SO:0000460"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C_gene_segment","synonyms":[{"name":"C gene","type":"exact"},{"name":"C_GENE","type":"exact"},{"name":"INSDC_feature:C_region","type":"exact"},{"name":"constant gene","type":"exact"}],"termid":"SO:0000478"}


id: MONDO:0009326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Heart block that occurs on or before 28 days of life.","definition_xrefs":["PMID:22368629"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete genetic cardiac rhythm disease (obsolete MONDO:0015110)","termid":"MONDO:0015110"},{"relation_name":"is_a","term_name":"atrioventricular block","termid":"MONDO:0000465"}],"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":"congenital heart block","secondary_identifiers":["OMIM:234700","ICD10CM:Q24.6","MESH:C535758","DOID:990","icd11.foundation:1096954866","MedDRA:10019263","ICD9:746.86","MEDGEN:57432","NORD:1218","Orphanet:60041","NANDO:2200214","SCTID:46619002","UMLS:C0149530","GARD:6164"],"synonyms":[{"name":"congenital atrioventricular block","type":"exact"},{"name":"heart block, congenital","type":"related"}],"termid":"MONDO:0009326","xrefs":{"Monarch":{"xref_id":"0009326"}}}


id: GO:0141095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A retrotransposon silencing mechanism in which a methylated cytosine residues in the genome promote heterochromatin assembly. Heterochromatin is a chromatin conformation that is refractory to transcription.","definition_xrefs":["PMID:15318244"],"gene_count":0,"genotype_count":0,"name":"obsolete retrotransposon silencing by DNA methylation-dependent heterochromatin formation (obsolete GO:0141095)","termid":"GO:0141095"}


id: MONDO:0015804
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A botulism that occurs between 28 days to one year of life..","definition_xrefs":["MONDO:patterns/infantile"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal botulism","termid":"MONDO:0015805"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infant botulism","secondary_identifiers":["DOID:0050354","NCIT:C128343","MEDGEN:68649","ICD10CM:A48.51","Orphanet:178478","SCTID:414488002","UMLS:C0238027","GARD:20150"],"synonyms":[{"name":"botulism of infancy","type":"exact"},{"name":"infant intestinal botulism","type":"exact"},{"name":"infant intestinal toxaemia botulism","type":"exact"},{"name":"infant intestinal toxemia botulism","type":"exact"},{"name":"infant intestinal toxin-mediated botulism","type":"exact"},{"name":"infantile botulism","type":"exact"},{"name":"infantile onset botulism","type":"exact"}],"termid":"MONDO:0015804","xrefs":{"Monarch":{"xref_id":"0015804"}}}


id: PBO:0048635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gap junction protein alpha 4","termid":"PBO:0048635"}


id: FYPO:0007271
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 nuclear chromatin organization is abnormal, such regions containing transposons (Tf2 elements) are tethered to the centromere to a greater extent than normal.","definition_xrefs":["PMID:23084836","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin organization during vegetative growth","termid":"FYPO:0001352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000641","FYPO:0005447","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased Tf body tethering to centromere","synonyms":[{"name":"increased Tf body tethering to centromere during mitotic cell cycle","type":"related"},{"name":"increased Tf body tethering to centromere during vegetative growth","type":"exact"},{"name":"increased Tf2 body tethering to centromere","type":"exact"},{"name":"increased centromere tethering of Tf2 bodies","type":"exact"}],"termid":"FYPO:0007271"}


id: PBO:0116781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ventricular heart development associated lncRNA","termid":"PBO:0116781"}


id: PBO:0057923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3648-2","termid":"PBO:0057923"}


id: PBO:0082099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"8-oxo-dGTP diphosphatase; prevents spontaneous mutagenesis via sanitization of oxidized purine nucleoside triphosphates; can also act as peroxisomal pyrophosphatase with specificity for coenzyme A and CoA derivatives, may function to remove potentially toxic oxidized CoA disulfide from peroxisomes to maintain the capacity for beta-oxidation of fatty acids; nudix hydrolase family member; similar E. coli MutT and human, rat and mouse MTH1","termid":"PBO:0082099"}


id: GO:0014745
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of muscle adaptation.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle adaptation","termid":"GO:0043502"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"muscle adaptation","termid":"GO:0043500"}],"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 muscle adaptation","synonyms":[{"name":"negative regulation of muscle plasticity","type":"related"}],"termid":"GO:0014745"}


id: MONDO:1011980
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinal dystrophy, non-human animal","secondary_identifiers":["OMIA:000869"],"termid":"MONDO:1011980","xrefs":{"Monarch":{"xref_id":"1011980"}}}


id: PBO:0113085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic aspartyl aminopeptidase with possible vacuole function; targeted to vacuole via Vps10p-dependent endosomal vacuolar protein sorting pathway and via CVT pathway; cleaves unblocked N-terminal acidic amino acids from peptide substrates; forms 12-subunit homo-oligomer; M18 metalloprotease family","termid":"PBO:0113085"}


id: PBO:0075134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein U1 subunit 70","termid":"PBO:0075134"}


id: MONDO:1010907
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Central core myopathy that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central core myopathy, non-human animal","termid":"MONDO:1010192"},{"relation_name":"is_a","term_name":"myofibrillar myopathy, horse","termid":"MONDO:1010936"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"central core myopathy, horse","secondary_identifiers":["OMIA:000172-9796"],"termid":"MONDO:1010907","xrefs":{"Monarch":{"xref_id":"1010907"}}}


id: FYPO:0002460
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is viable, branched, septated, elongated, and is curved along the long axis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable curved elongated vegetative cell","termid":"FYPO:0002215"},{"relation_name":"is_a","term_name":"viable branched, elongated vegetative cell","termid":"FYPO:0002459"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000004"],"is_obsolete":false,"name":"viable branched, curved, elongated vegetative cell","secondary_identifiers":["FYPO:0002477"],"synonyms":[{"name":"viable branched curved cell","type":"exact"},{"name":"viable branched, curved cell during vegetative growth","type":"exact"},{"name":"viable branched, curved septated cell","type":"exact"},{"name":"viable branched, curved vegetative cell","type":"exact"},{"name":"viable branched, curved vegetative cell during mitotic cell cycle","type":"related"},{"name":"viable branched, curved, elongated cell during vegetative growth","type":"exact"},{"name":"viable branched, curved, elongated vegetative cell during mitotic cell cycle","type":"related"},{"name":"viable branched, elongated, curved septated cell","type":"exact"},{"name":"viable branched, long, curved, septated cell","type":"exact"},{"name":"viable curved branched cell","type":"exact"},{"name":"viable elongated branched curved cell","type":"exact"}],"termid":"FYPO:0002460"}


id: GO:0017119
data:
  {"annotated_genes":["SJAG_00041","SJAG_00578","SJAG_03054","SJAG_01071","SJAG_02211","SJAG_01459","SJAG_03158"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[69970,70704,75681,77713,89302,109803,117129],"is_not":false,"summary":null,"term":"GO:0017119"}]},"cv_name":"cellular_component","definition":"A multisubunit tethering complex of the CATCHR family (complexes associated with tethering containing helical rods) that has a role in tethering vesicles to the Golgi prior to fusion. Composed of 8 subunits COG1-8.","definition_xrefs":["PMID:11980916","GOC:krc","PMID:20972446","PMID:9792665"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle tethering complex","termid":"GO:0099023"},{"relation_name":"part_of","term_name":"Golgi apparatus","termid":"GO:0005794"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00041":null,"SJAG_00578":null,"SJAG_01071":null,"SJAG_01459":null,"SJAG_02211":null,"SJAG_03054":null,"SJAG_03158":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737","GO:0005794"],"is_obsolete":false,"name":"Golgi transport complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"COG complex","type":"exact"},{"name":"Sec34/35 complex","type":"narrow"},{"name":"conserved oligomeric Golgi complex","type":"exact"}],"termid":"GO:0017119","terms_by_termid":{"GO:0017119":null}}


id: PBO:0003936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic recombination protein Rec15","termid":"PBO:0003936"}


id: PBO:0043776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxypeptidase A2","termid":"PBO:0043776"}


id: GO:1904274
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a tricellular tight junction.","definition_xrefs":["GO_REF:0000079","PMID:4203962","GOC:TermGenie","GOC:mr","PMID:25097825","PMID:22640933"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tight junction assembly","termid":"GO:0120192"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"tricellular tight junction assembly","synonyms":[{"name":"tricellular tight junction formation","type":"exact"}],"termid":"GO:1904274"}


id: MONDO:0009390
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":"hyperlysinuria with hyperammonemia","secondary_identifiers":["MEDGEN:120650","SCTID:342553006","ICD9:270.7","OMIM:238750","UMLS:C0268555"],"synonyms":[{"name":"hyperlysinemia, periodic","type":"related"},{"name":"hyperlysinuria with hyperammonemia","type":"exact"}],"termid":"MONDO:0009390","xrefs":{"Monarch":{"xref_id":"0009390"}}}


id: PBO:0079332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 18","termid":"PBO:0079332"}


id: GO:0090518
data:
  {"annotated_genes":["SJAG_03256"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104147],"is_not":false,"summary":null,"term":"GO:0090518"}]},"cv_name":"biological_process","definition":"The directed movement of L-arginine into the vacuole across the vacuolar membrane.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"basic amino acid transmembrane import into vacuole","termid":"GO:0034490"},{"relation_name":"is_a","term_name":"L-arginine transmembrane transport","termid":"GO:1903826"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03256":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"L-arginine transmembrane import into vacuole","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0090458"],"synonyms":[{"name":"arginine transmembrane import into vacuole","type":"broad"},{"name":"vacuolar arginine import","type":"exact"}],"termid":"GO:0090518","terms_by_termid":{"GO:0090518":null}}


id: GO:0045328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent linkage of heme to cytochrome P450 4A1 via hydroxyheme-L-glutamyl ester.","definition_xrefs":["RESID:AA0324","GOC:cjm"],"gene_count":0,"genotype_count":0,"name":"obsolete cytochrome P450 4A1-heme linkage (obsolete GO:0045328)","synonyms":[{"name":"cytochrome P450 4A1-haem linkage","type":"exact"}],"termid":"GO:0045328"}


id: PBO:0086936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab family GTPase involved in the exocytic pathway; mediates intra-Golgi traffic or the budding of post-Golgi vesicles from the trans-Golgi; protein abundance increases in response to DNA replication stress; YPT32 has a paralog, YPT31, that arose from the whole genome duplication","termid":"PBO:0086936"}


id: PBO:0047026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 91 member A1","termid":"PBO:0047026"}


id: MONDO:0017376
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Reactive arthritis (ReA) is an autoimmune disorder belonging to the group of seronegative spondyloarthropathies and is characterized by the classic triad of arthritis, urethritis and conjunctivitis.","definition_xrefs":["Orphanet:29207"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rheumatic disorder","termid":"MONDO:0005554"},{"relation_name":"is_a","term_name":"arthritic joint disease","termid":"MONDO:0005578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reactive arthritis","secondary_identifiers":["DOID:6196","NORD:1650","ICD9:099.3","MedDRA:10003267","MEDGEN:39047","MESH:D016918","SCTID:129133005","MedDRA:10038294","NCIT:C128332","GARD:5693","ICD9:711.40","ICD9:711.30","ICD9:711.3","UMLS:C0085435","EFO:0007460"],"synonyms":[{"name":"Fiessinger Leroy Reiter syndrome","type":"exact"},{"name":"Fiessinger-Leroy disease","type":"exact"},{"name":"Fiessinger-Leroy-Reiter syndrome","type":"exact"},{"name":"PIRA","type":"related"},{"name":"Reiter disease","type":"exact"},{"name":"Reiter syndrome","type":"exact"},{"name":"Reiter's disease","type":"exact"},{"name":"Reiter's syndrome","type":"exact"},{"name":"arthritis urethritica","type":"exact"},{"name":"polyarthritis enterica","type":"exact"},{"name":"post-bacterial arthropathy","type":"exact"},{"name":"post-infectious arthritis","type":"related"},{"name":"post-infectious reactive arthropathy","type":"related"},{"name":"postdysenteric arthropathy","type":"exact"},{"name":"reactive arthritis","type":"exact"},{"name":"venereal arthritis","type":"exact"}],"termid":"MONDO:0017376","xrefs":{"Monarch":{"xref_id":"0017376"}}}


id: MONDO:0008740
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Agnathia-holoprosencephaly-situs inversus syndrome is an extremely rare and fatal association syndrome, characterized by absence of the mandible, cerebral malformations with facial anomalies related to a defect in cleavage in the embryonic brain (e.g. synophthalmia, malformed and low-set ears fused in midline (otocephaly), agenesis of the olfactory bulbs, microstomia, hypoglossia/aglossia) and situs inversus partialis or totalis.","definition_xrefs":["Orphanet:990"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"agnathia-otocephaly complex","secondary_identifiers":["NCIT:C124568","UMLS:C0265242","OMIM:202650","MEDGEN:78541","GARD:9126","DOID:0060341","SCTID:48180002","ICD9:759.89"],"synonyms":[{"name":"AGOTC","type":"related"},{"name":"Dysgnathia Complex agnathia-holoprosencephaly","type":"related"},{"name":"agnathia-holoprosencephaly","type":"related"},{"name":"agnathia-holoprosencephaly-situs inversus syndrome","type":"exact"},{"name":"agnathia-otocephaly complex","type":"exact"},{"name":"dysgnathia complex agnathia-holoprosencephaly","type":"exact"},{"name":"holoprosencephaly-agnathia","type":"exact"},{"name":"otocephaly","type":"exact"}],"termid":"MONDO:0008740","xrefs":{"Monarch":{"xref_id":"0008740"}}}


id: PBO:0072855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretion associated Ras related GTPase 1B","termid":"PBO:0072855"}


id: PBO:0057633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1208","termid":"PBO:0057633"}


id: GO:0034919
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-methyl-3-oxohexanoyl-CoA + CoA = propanoyl-CoA + butyryl-CoA.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete butyryl-CoA 2-C-propionyltransferase activity (obsolete GO:0034919)","termid":"GO:0034919"}


id: MONDO:0011021
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neuronal intestinal dysplasia","termid":"MONDO:0000858"},{"relation_name":"is_a","term_name":"chronic intestinal pseudoobstruction","termid":"MONDO:0017574"}],"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":"neuronal intestinal dysplasia, type B","secondary_identifiers":["DOID:0080680","UMLS:C1832589","MEDGEN:318658","OMIM:601223"],"synonyms":[{"name":"NID B","type":"exact"},{"name":"neuronal intestinal dysplasia, type B","type":"exact"}],"termid":"MONDO:0011021","xrefs":{"Monarch":{"xref_id":"0011021"}}}


id: GO:0019214
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. The action of reducing the surface tension of a liquid.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete surfactant activity (obsolete GO:0019214)","synonyms":[{"name":"surfactant activity","type":"exact"}],"termid":"GO:0019214"}


id: RO:0002010
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x 'regulates in other organism' y if and only if: (x is the realization of a function to exert an effect on the frequency, rate or extent of y) AND (the agents of x are produced by organism o1 and the agents of y are produced by organism o2).","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_upstream_of_or_within","termid":"RO:0002418"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulates_in_other_organism","termid":"RO:0002010"}


id: MONDO:0011761
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 6p24.1-p22.3.","definition_xrefs":["DOID:0110551","PMID:10764236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 21","secondary_identifiers":["GARD:18116","MESH:C564634","MEDGEN:339643","OMIM:607017","UMLS:C1846922"],"synonyms":[{"name":"DFNA21","type":"narrow"},{"name":"autosomal dominant deafness 21","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 21","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 21","type":"narrow"},{"name":"deafness, autosomal dominant 21","type":"narrow"}],"termid":"MONDO:0011761","xrefs":{"Monarch":{"xref_id":"0011761"}}}


id: GO:0099074
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Vesicle-mediated transport of cargo from the mitochondrion to the lysosome, mediated by a mitochondrion-derived vesicle.","definition_xrefs":["GOC:PARL-UCL","GOC:pad","PMID:20619655","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal transport","termid":"GO:0007041"},{"relation_name":"is_a","term_name":"mitochondrion-derived vesicle mediated transport","termid":"GO:0099075"}],"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:0016192"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"mitochondrion to lysosome vesicle-mediated transport","synonyms":[{"name":"mitochondrion to lysosome transport","type":"exact"}],"termid":"GO:0099074"}


id: CHEBI:37903
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":"lysyl group","termid":"CHEBI:37903"}


id: PBO:0017924
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nemaline Myopathy","termid":"PBO:0017924"}


id: GO:0002306
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a CD4-positive, gamma-delta intraepithelial T cell. Intraepithelial T cells are found among epithelial cells in mucosal areas and have distinct phenotypes and developmental pathways.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gamma-delta intraepithelial T cell differentiation","termid":"GO:0002304"}],"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":"CD4-positive gamma-delta intraepithelial T cell differentiation","synonyms":[{"name":"CD4-positive, gamma-delta intraepithelial T cell development","type":"related"},{"name":"CD4-positive, gamma-delta intraepithelial T lymphocyte differentiation","type":"exact"},{"name":"CD4-positive, gamma-delta intraepithelial T-cell differentiation","type":"exact"},{"name":"CD4-positive, gamma-delta intraepithelial T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002306"}


id: PBO:0064051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 85","termid":"PBO:0064051"}


id: GO:0019435
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sophorosyloxydocosanoate, 13-sophorosyloxydocosanoate 6',6''-diacetate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolipid biosynthetic process","termid":"GO:0009247"},{"relation_name":"is_a","term_name":"sophorosyloxydocosanoate metabolic process","termid":"GO:0019434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"sophorosyloxydocosanoate biosynthetic process","secondary_identifiers":["MetaCyc:SOPHOROSYLOXYDOCOSANOATE-SYN-PWY"],"synonyms":[{"name":"sophorosyloxydocosanoate anabolism","type":"exact"},{"name":"sophorosyloxydocosanoate biosynthesis","type":"exact"},{"name":"sophorosyloxydocosanoate formation","type":"exact"},{"name":"sophorosyloxydocosanoate synthesis","type":"exact"}],"termid":"GO:0019435"}


id: MONDO:1010967
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dandy-Walker syndrome that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Dandy-Walker syndrome, non-human animal","termid":"MONDO:1010228"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dandy-Walker syndrome, sheep","secondary_identifiers":["OMIA:000258-9940"],"termid":"MONDO:1010967","xrefs":{"Monarch":{"xref_id":"1010967"}}}


id: GO:0022025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of leukemia inhibitory factor to its receptor on the surface of the target cell, that contributes to the commitment of a neuroblast to a neuronal fate. The neuron will reside in the forebrain.","definition_xrefs":["GOC:dph","GOC:signaling","GOC:jid","GOC:cls","GOC:dgh","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukemia inhibitory factor signaling pathway","termid":"GO:0048861"},{"relation_name":"part_of","term_name":"commitment of multipotent stem cells to neuronal lineage in forebrain","termid":"GO:0021898"}],"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":"leukemia inhibitory factor signaling pathway involved in forebrain neuron fate commitment","synonyms":[{"name":"leukemia inhibitory factor signalling pathway involved in forebrain neuron fate commitment","type":"exact"}],"termid":"GO:0022025"}


id: MONDO:0004790
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A reversible condition wherein large vacuoles of triglyceride fat accumulate in liver cells via the process of steatosis.","definition_xrefs":["Wikipedia:Fatty_liver"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver disorder","termid":"MONDO:0005154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"fatty liver disease","secondary_identifiers":["MESH:D005234","UMLS:C2711227","ICD9:571.0","SCTID:197321007","MEDGEN:398225","ICD9:571.8","DOID:9452","SCTID:371330000"],"synonyms":[{"name":"fatty change of liver","type":"exact"},{"name":"fatty liver","type":"exact"},{"name":"hepatic lipidosis","type":"exact"},{"name":"steatosis of liver","type":"exact"}],"termid":"MONDO:0004790","xrefs":{"Monarch":{"xref_id":"0004790"}}}


id: GO:0043190
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex for the transport of metabolites into and out of the cell, typically comprised of four domains; two membrane-associated domains and two ATP-binding domains at the intracellular face of the membrane, that form a central pore through the plasma membrane. Each of the four core domains may be encoded as a separate polypeptide or the domains can be fused in any one of a number of ways into multidomain polypeptides. In Bacteria and Archaebacteria, ABC transporters also include substrate binding proteins to bind substrate external to the cytoplasm and deliver it to the transporter.","definition_xrefs":["PMID:11421269","GOC:jl","GOC:mtg_sensu","PMID:15111107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase dependent transmembrane transport complex","termid":"GO:0098533"},{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"ATP-binding cassette (ABC) transporter complex","secondary_identifiers":["GO:0043192","GO:0043191"],"synonyms":[{"name":"ABC-type efflux permease complex","type":"narrow"},{"name":"ABC-type efflux porter complex","type":"narrow"},{"name":"ABC-type uptake permease complex","type":"narrow"},{"name":"mating pheromone exporter","type":"narrow"}],"termid":"GO:0043190"}


id: MONDO:0011084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"psoriasis, susceptibility to","termid":"MONDO:0100171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psoriasis 3, susceptibility to","secondary_identifiers":["UMLS:C1832345","DOID:0111283","MEDGEN:316964","OMIM:601454"],"synonyms":[{"name":"PSORS3","type":"exact"},{"name":"psoriasis 3, susceptibility to","type":"exact"},{"name":"psoriasis susceptibility 3","type":"exact"}],"termid":"MONDO:0011084","xrefs":{"Monarch":{"xref_id":"0011084"}}}


id: PBO:0074222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 45 member 1","termid":"PBO:0074222"}


id: PR:Q10496
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A TBC1 domain family member 2B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase activating protein Gyp51 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26F1.09","secondary_identifiers":["UniProtKB:Q10496"],"synonyms":[{"name":"SPAC26F1.09","type":"related"},{"name":"Spom972h-TBC1D2B","type":"exact"}],"termid":"PR:Q10496"}


id: PBO:0070338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY4 pseudogene 10","termid":"PBO:0070338"}


id: MONDO:0019629
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A corneal disease in which the cornea blends with sclera, resulting in clouding of the cornea.","definition_xrefs":["PMID:3994576","DOID:0060252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corneal disorder","termid":"MONDO:0000942"}],"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":"sclerocornea","secondary_identifiers":["GARD:16800","MEDGEN:344000","icd11.foundation:995798428","Orphanet:91490","MESH:C565209","HP:0000647","UMLS:C1853235"],"synonyms":[{"name":"isolated congenital sclerocornea","type":"exact"},{"name":"sclerocornea","type":"exact"},{"name":"sclerocornea (disease)","type":"exact"}],"termid":"MONDO:0019629","xrefs":{"Monarch":{"xref_id":"0019629"}}}


id: FYPO:0002809
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 6,7-dimethyl-8-ribityllumazine synthase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal 6,7-dimethyl-8-ribityllumazine synthase activity","termid":"FYPO:0002808"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000654","FYPO:0000707","FYPO:0000661","FYPO:0000652"],"is_obsolete":false,"name":"decreased 6,7-dimethyl-8-ribityllumazine synthase activity","synonyms":[{"name":"reduced 6,7-dimethyl-8-ribityllumazine synthase activity","type":"exact"}],"termid":"FYPO:0002809"}


id: PBO:0087680
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 Mgr1p that binds to substrates to facilitate proteolysis; required for growth of cells lacking mtDNA","termid":"PBO:0087680"}


id: GO:0033628
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of cell adhesion mediated by integrin.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell adhesion","termid":"GO:0030155"},{"relation_name":"regulates","term_name":"cell adhesion mediated by integrin","termid":"GO:0033627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"regulation of cell adhesion mediated by integrin","synonyms":[{"name":"regulation of cell adhesion mediated by integrin complex","type":"exact"}],"termid":"GO:0033628"}


id: PBO:0061272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADPH oxidase 4","termid":"PBO:0061272"}


id: PBO:0043442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calponin 2 pseudogene 2","termid":"PBO:0043442"}


id: GO:0047291
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cytolipin-H + CMP-N-acetylneuraminate = alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,4-beta-D-glucosylceramide + CMP. Alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,4-beta-D-glucosylceramide is also known as GM3.","definition_xrefs":["MetaCyc:2.4.99.9-RXN","EC:2.4.3.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sialyltransferase activity","termid":"GO:0008373"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016757","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"lactosylceramide alpha-2,3-sialyltransferase activity","secondary_identifiers":["RHEA:18417"],"synonyms":[{"name":"CMP-acetylneuraminate-lactosylceramide-sialyltransferase","type":"broad"},{"name":"GM3 synthase activity","type":"related"},{"name":"cytidine monophosphoacetylneuraminate-lactosylceramide alpha2,3- sialyltransferase activity","type":"related"},{"name":"cytidine monophosphoacetylneuraminate-lactosylceramide sialyltransferase","type":"broad"},{"name":"ganglioside GM3 synthase activity","type":"related"}],"termid":"GO:0047291"}


id: GO:0042350
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of GDP-L-fucose, a substance composed of L-fucose in glycosidic linkage with guanosine diphosphate.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar biosynthetic process","termid":"GO:0009226"},{"relation_name":"is_a","term_name":"GDP-L-fucose metabolic process","termid":"GO:0046368"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"GDP-L-fucose biosynthetic process","secondary_identifiers":["Reactome:R-HSA-6787639"],"synonyms":[{"name":"GDP-L-fucose anabolism","type":"exact"},{"name":"GDP-L-fucose biosynthesis","type":"exact"},{"name":"GDP-L-fucose formation","type":"exact"},{"name":"GDP-L-fucose synthesis","type":"exact"}],"termid":"GO:0042350"}


id: PBO:0067986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 288","termid":"PBO:0067986"}


id: GO:0090230
data:
  {"annotated_genes":["SJAG_03048","SJAG_01837","SJAG_04638","SJAG_00718"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905560"},{"annotations":[89990,116972,102692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905561"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of centromere complex assembly, the aggregation, arrangement and bonding together of proteins and centromeric DNA molecules to form a centromeric protein-DNA complex.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chromosome organization","termid":"GO:0033044"},{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"regulates","term_name":"centromere complex assembly","termid":"GO:0034508"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00718":null,"SJAG_01837":null,"SJAG_03048":null,"SJAG_04638":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"regulation of centromere complex assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"centromere licensing","type":"related"}],"termid":"GO:0090230","terms_by_termid":{"GO:1905560":null,"GO:1905561":null}}


id: GO:0010543
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate or frequency of platelet activation. Platelet activation is a series of progressive, overlapping events triggered by exposure of the platelets to subendothelial tissue.","definition_xrefs":["GOC:tb","GOC:dph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell activation","termid":"GO:0050865"},{"relation_name":"regulates","term_name":"platelet activation","termid":"GO:0030168"}],"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 platelet activation","termid":"GO:0010543"}


id: GO:0052804
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of nitroimidazoles, imidazole derivatives with a nitro group attached to one ring.","definition_xrefs":["PMID:19039139","PMID:16387854"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imidazole-containing compound catabolic process","termid":"GO:0052805"}],"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":"nitroimidazole catabolic process","synonyms":[{"name":"nitroimidazole breakdown","type":"exact"},{"name":"nitroimidazole catabolism","type":"exact"},{"name":"nitroimidazole degradation","type":"exact"}],"termid":"GO:0052804"}


id: GO:0043530
data:
  {"annotated_genes":["SJAG_01231"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[114994],"is_not":false,"summary":null,"term":"GO:0043530"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: adenosine 5'-monophosphoramidate + H2O = AMP + NH4+. Other substrates include AMP-morpholidate, AMP-N-alanine methyl ester and AMP-alpha-acetyl lysine methyl ester.","definition_xrefs":["PMID:11805111","RHEA:67916"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01231":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"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:0003824","GO:0016787","GO:0016810"],"is_obsolete":false,"name":"adenosine 5'-monophosphoramidase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"adenosine 5' monophosphoramidase activity","type":"exact"},{"name":"adenosine 5'-monophosphoramidate hydrolase activity","type":"exact"}],"termid":"GO:0043530","terms_by_termid":{"GO:0043530":null}}


id: GO:0039665
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Induction of organellar membrane permeabilization triggered by an interaction between the host membrane and a membrane-penetration protein associated with a viral capsid. Results in release of the virus contents from an organelle into the host cell cytoplasm.","definition_xrefs":["VZ:985","GOC:bf","GOC:jl","UniProtKB-KW:KW-1173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"},{"relation_name":"part_of","term_name":"symbiont entry into host cell via permeabilization of host membrane","termid":"GO:0140267"}],"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":"permeabilization of host organelle membrane involved in viral entry into host cell","synonyms":[{"name":"viral entry into host cell via permeabilization of host organelle membrane","type":"related"},{"name":"viral membrane-penetration protein","type":"related"},{"name":"viral penetration via host endosomal membrane disruption by virus","type":"exact"},{"name":"viral penetration via perforation of host organellar membrane by virus","type":"exact"},{"name":"viral penetration via permeabilization of host organellar membrane","type":"exact"}],"termid":"GO:0039665"}


id: MONDO:0012236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"keratoconus","termid":"MONDO:0015486"}],"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":"keratoconus 4","secondary_identifiers":["UMLS:C1836473","MESH:C563752","OMIM:609271","MEDGEN:332217"],"synonyms":[{"name":"KTCN4","type":"exact"},{"name":"keratoconus 4","type":"exact"}],"termid":"MONDO:0012236","xrefs":{"Monarch":{"xref_id":"0012236"}}}


id: GO:2001131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a methane from a dimethyl sulfide.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"methanogenesis","termid":"GO:0015948"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0008150","GO:0006091","GO:0006790"],"is_obsolete":false,"name":"methane biosynthetic process from dimethyl sulfide","termid":"GO:2001131"}


id: GO:0098855
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cation ion channel with a preference for K+ over Na+ ions, which is activated by membrane hyperpolarization, and consists of a tetramer of HCN family members. Some members of this family (HCN1, HCN2 and HCN4) are also activated when cAMP binds to their cyclic nucleotide binding domain (CNBD). Channel complexes of this family play an important role in the control of pacemaker activity in the heart.","definition_xrefs":["PMID:20829353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel complex","termid":"GO:0008076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"HCN channel complex","secondary_identifiers":["GO:1990746","GO:1990759"],"synonyms":[{"name":"HCN1 channel complex","type":"narrow"},{"name":"HCN2 channel complex","type":"narrow"},{"name":"HCN3 channel complex","type":"narrow"},{"name":"HCN4 channel complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated channel 3 complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated cyclic nucleotide-gated channel 1 complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated cyclic nucleotide-gated channel 2 complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated cyclic nucleotide-gated channel 4 complex","type":"narrow"},{"name":"K/Na hyperpolarization-activated cyclic nucleotide-gated channel complex","type":"exact"},{"name":"potassium/sodium hyperpolarization-activated channel 3 complex","type":"narrow"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 complex","type":"narrow"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 complex","type":"narrow"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2 tetramer","type":"related"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 complex","type":"narrow"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 tetramer","type":"related"},{"name":"potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel complex","type":"exact"}],"termid":"GO:0098855"}


id: GO:0099645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a neurotransmitter is transported to, or maintained in, a location within the membrane adjacent to a postsynaptic specialization (e.g. postsynaptic density).","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor localization to synapse","termid":"GO:0097120"},{"relation_name":"is_a","term_name":"regulation of postsynaptic membrane neurotransmitter receptor levels","termid":"GO:0099072"},{"relation_name":"is_a","term_name":"protein localization to postsynaptic specialization membrane","termid":"GO:0099633"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"neurotransmitter receptor localization to postsynaptic specialization membrane","synonyms":[{"name":"neurotransmitter receptor localisation in postsynaptic specialization membrane","type":"exact"}],"termid":"GO:0099645"}


id: PBO:0065879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB30, member RAS oncogene family","termid":"PBO:0065879"}


id: FYPO:0007745
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which assembly of the meiotic spindle is abnormal during the first meiotic nuclear division.","definition_xrefs":["PMID:32723864","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle assembly","termid":"FYPO:0000737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000054","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal spindle assembly during meiosis I","synonyms":[{"name":"abnormal meiosis I spindle assembly","type":"exact"},{"name":"abnormal meiosis I spindle formation","type":"exact"},{"name":"abnormal meiotic spindle assembly during meiosis I","type":"exact"}],"termid":"FYPO:0007745"}


id: PBO:0055242
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 2669","termid":"PBO:0055242"}


id: MONDO:0022941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deafness hypospadias metacarpal and metatarsal syndrome","termid":"MONDO:0022941","xrefs":{"Monarch":{"xref_id":"0022941"}}}


id: PBO:0083336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps the telomere on the right arm of chromosome 13","termid":"PBO:0083336"}


id: GO:1904916
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of L-lysine from the lysosomal lumen across the lysosomal membrane and into the cytosol.","definition_xrefs":["GO_REF:0000078","GOC:kmv","GOC:TermGenie","PMID:22822152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-lysine transmembrane export from vacuole","termid":"GO:0089707"},{"relation_name":"is_a","term_name":"transmembrane transport from lysosomal lumen to cytosol","termid":"GO:0170063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"L-lysine transmembrane transport from lysosomal lumen to cytosol","synonyms":[{"name":"transmembrane L-lysine transport from lysosomal lumen to cytosol","type":"exact"}],"termid":"GO:1904916"}


id: FYPO:0000981
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutamate dehydrogenase activity using NAD+ as a cofactor 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:0000257"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"normal glutamate dehydrogenase (NAD+) activity","synonyms":[{"name":"normal NAD-GDH activity","type":"exact"}],"termid":"FYPO:0000981"}


id: GO:0033853
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-arogenate + oxaloacetate = prephenate + L-aspartate.","definition_xrefs":["RHEA:20445"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016769","GO:0003674"],"is_obsolete":false,"name":"aspartate-prephenate aminotransferase activity","secondary_identifiers":["EC:2.6.1.78","MetaCyc:PREPHENATE-ASP-TRANSAMINE-RXN"],"synonyms":[{"name":"L-arogenate:oxaloacetate aminotransferase activity","type":"related"},{"name":"L-aspartate:prephenate aminotransferase activity","type":"related"},{"name":"PAT","type":"related"},{"name":"prephenate aspartate aminotransferase activity","type":"related"},{"name":"prephenate transaminase activity","type":"broad"}],"termid":"GO:0033853"}


id: PBO:0054758
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 2169","termid":"PBO:0054758"}


id: GO:1902737
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small, membranous protrusion found primarily on dendritic stretches of developing neurons. May receive synaptic input, and can develop into dendritic spines.","definition_xrefs":["GO_REF:0000064","GOC:PARL","GOC:pad","PMID:24464040","GOC:TermGenie","Wikipedia:Dendritic_filopodia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"filopodium","termid":"GO:0030175"},{"relation_name":"is_a","term_name":"neuron projection","termid":"GO:0043005"},{"relation_name":"part_of","term_name":"dendrite","termid":"GO:0030425"}],"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":"dendritic filopodium","synonyms":[{"name":"dendrite filopodium","type":"exact"}],"termid":"GO:1902737"}


id: PBO:0082486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Carnitine acetyltransferase; has similarity to Yat1p, which is a carnitine acetyltransferase associated with the mitochondrial outer membrane","termid":"PBO:0082486"}


id: PBO:0065440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, ATPase 1 pseudogene 13","termid":"PBO:0065440"}


id: FYPO:0002191
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, is shaped in the form of a spheroid, has one or more septa, and has a larger volume than normal. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable swollen spheroid vegetative cell","termid":"FYPO:0002190"},{"relation_name":"is_a","term_name":"swollen septated spheroid vegetative cell","termid":"FYPO:0002240"},{"relation_name":"is_a","term_name":"inviable septated vegetative cell with abnormal cell morphology","termid":"FYPO:0002452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000004","FYPO:0000005","FYPO:0001320"],"is_obsolete":false,"name":"inviable swollen septated spheroid vegetative cell","synonyms":[{"name":"inviable enlarged septated spheroid vegetative cell","type":"related"},{"name":"inviable enlarged volume septated spheroid vegetative cell","type":"exact"},{"name":"inviable septated large spheroid vegetative cell","type":"related"},{"name":"inviable swollen septated rounded vegetative cell","type":"exact"},{"name":"inviable swollen septated spheroid cell during vegetative growth","type":"exact"},{"name":"inviable swollen septated spheroid vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable, septated, increased spheroid vegetative cell size","type":"related"},{"name":"inviable, septated, increased spheroid vegetative cell volume","type":"exact"},{"name":"lethal; swollen septated spheroid vegetative cell","type":"exact"}],"termid":"FYPO:0002191"}


id: PBO:0111861
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTB/POZ domain","termid":"PBO:0111861"}


id: GO:0034528
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-carboxy-2-hydroxy-8-carboxychromene = 2-hydroxy-3-carboxybenzalpyruvate.","definition_xrefs":["UM-BBD_reactionID:r0791"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-carboxy-2-hydroxy-8-carboxychromene isomerase activity (obsolete GO:0034528)","termid":"GO:0034528"}


id: GO:0061316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes that contributes to the progression of the heart over time. In this pathway, the activated receptor signals via downstream effectors that result in the inhibition of beta-catenin phosphorylation, thereby preventing degradation of beta-catenin. Stabilized beta-catenin can then accumulate and travel to the nucleus to trigger changes in transcription of target genes.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Wnt signaling pathway involved in heart development","termid":"GO:0003306"},{"relation_name":"is_a","term_name":"canonical Wnt signaling pathway","termid":"GO:0060070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"canonical Wnt signaling pathway involved in heart development","synonyms":[{"name":"canonical Wnt receptor signaling pathway involved in heart development","type":"exact"},{"name":"canonical Wnt receptor signalling pathway involved in heart development","type":"exact"},{"name":"canonical Wnt-activated signaling pathway involved in heart development","type":"exact"}],"termid":"GO:0061316"}


id: PBO:0058389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4761","termid":"PBO:0058389"}


id: PBO:0087233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sensor-transducer of the stress-activated PKC1-MPK1 kinase pathway; involved in maintenance of cell wall integrity; required for mitophagy; involved in organization of the actin cytoskeleton; secretory pathway Wsc1p is required for the arrest of secretion response","termid":"PBO:0087233"}


id: PBO:0055637
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 3076","termid":"PBO:0055637"}


id: MONDO:0016418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple system atrophy, cerebellar type (MSA-c) is a form of multiple system atrophy (MSA) with predominant cerebellar features (gait and limb ataxia, oculomotor dysfunction, and dysarthria).","definition_xrefs":["Orphanet:227510"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-hereditary degenerative ataxia (obsolete MONDO:0016592)","termid":"MONDO:0016592"},{"relation_name":"is_a","term_name":"multiple system atrophy","termid":"MONDO:0007803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0021179"],"is_obsolete":false,"name":"multiple system atrophy, cerebellar type","secondary_identifiers":["MEDGEN:1843304","GARD:20565","icd11.foundation:1585600114","NANDO:1200035","UMLS:C5554234"],"synonyms":[{"name":"MSA, cerebellar type","type":"exact"},{"name":"MSA-c","type":"exact"},{"name":"sporadic OPCA type 1","type":"exact"},{"name":"sporadic olivopontocerebellar atrophy type 1","type":"exact"}],"termid":"MONDO:0016418","xrefs":{"Monarch":{"xref_id":"0016418"}}}


id: PBO:0027116
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_premeiotic_DNA_replication_during_azygotic_meiosis","termid":"PBO:0027116"}


id: GO:0072435
data:
  {"annotated_genes":["SJAG_04332","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94882,102711],"is_not":false,"summary":null,"term":"GO:0072435"}]},"cv_name":"biological_process","definition":"A process that occurs in response to signals generated as a result of mitotic G2/M transition DNA damage checkpoint signaling.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to mitotic cell cycle checkpoint signaling","termid":"GO:0072414"},{"relation_name":"is_a","term_name":"response to G2 DNA damage checkpoint signaling","termid":"GO:0072426"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03048":null,"SJAG_04332":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to mitotic G2 DNA damage checkpoint signaling","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0072458"],"synonyms":[{"name":"mitotic G2/M transition DNA damage checkpoint effector process","type":"exact"},{"name":"mitotic G2/M transition decatenation checkpoint effector process","type":"related"},{"name":"response to mitotic G2/M transition DNA damage checkpoint signaling","type":"exact"},{"name":"response to mitotic G2/M transition decatenation checkpoint signaling","type":"related"},{"name":"response to signal involved in mitotic G2/M transition DNA damage checkpoint","type":"exact"},{"name":"response to signal involved in mitotic G2/M transition decatenation checkpoint","type":"related"}],"termid":"GO:0072435","terms_by_termid":{"GO:0072435":null}}


id: PBO:0083913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Forkhead family transcription factor; rate-limiting replication origin activator; evolutionarily conserved lifespan regulator; binds multiple chromosomal elements with distinct specificities, cell cycle dynamics; regulates transcription elongation, chromatin silencing at mating loci, expression of G2/M phase genes; facilitates clustering, activation of early-firing replication origins; binds HML recombination enhancer, regulates donor preference during mating-type switching","termid":"PBO:0083913"}


id: GO:0019073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The packing of viral DNA into a capsid.","definition_xrefs":["ISBN:0781702534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral genome packaging","termid":"GO:0019072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"viral DNA genome packaging","termid":"GO:0019073"}


id: PBO:0004346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial DNA repair protein (predicted)","termid":"PBO:0004346"}


id: PBO:0085369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphotyrosine-specific phosphatase; major role in osmolarity sensing through dephosphorylation of the Hog1p MAPK with a minor role by Ptp3p; inactivates and regulates Hog1p localization; major role in the cell wall integrity pathway through dephosphorylation of MAPK Slt2p with a minor role by Ptp3p; minor role with Msg5p in the pheromone adaptive response through dephosphorylation of MAPK Fus3p with major role by Ptp3p; co-regulates the calcium signaling pathway with Msg5p; nuclear localized","termid":"PBO:0085369"}


id: MONDO:0013745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the TMEM237 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome with oculorenal defect","termid":"MONDO:0009480"},{"relation_name":"is_a","term_name":"Joubert syndrome with ocular defect","termid":"MONDO:0016364"},{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0020022","MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"Joubert syndrome 14","secondary_identifiers":["OMIM:614424","GARD:15801","UMLS:C3280766","DOID:0110983","MEDGEN:482396"],"synonyms":[{"name":"JBTS14","type":"exact"},{"name":"Joubert syndrome 14","type":"exact"},{"name":"Joubert syndrome caused by mutation in TMEM237","type":"exact"},{"name":"Joubert syndrome type 14","type":"exact"},{"name":"TMEM237 Joubert syndrome","type":"exact"}],"termid":"MONDO:0013745","xrefs":{"Monarch":{"xref_id":"0013745"}}}


id: PR:O94418
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nuclear pore complex protein Nup93 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 87 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.11","secondary_identifiers":["UniProtKB:O94418"],"synonyms":[{"name":"Spom972h-NUP93","type":"exact"}],"termid":"PR:O94418"}


id: GO:0048757
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Steps required to form a membrane-bounded organelle into a pigment granule containing pigment. Maturation is a developmental process, independent of morphogenetic (shape) change, that is required for a cell or structure to attain its fully functional state.","definition_xrefs":["GOC:jid","GOC:dgh","GOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental maturation","termid":"GO:0021700"},{"relation_name":"is_a","term_name":"cellular pigment accumulation","termid":"GO:0043482"},{"relation_name":"part_of","term_name":"pigment cell differentiation","termid":"GO:0050931"}],"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":"pigment granule maturation","termid":"GO:0048757"}


id: MONDO:0700259
data:
  {"annotated_genes":["SJAG_02039"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012472"}]},"cv_name":"mondo","definition":"Any type 1 interferonopathies in which the cause of the disease is a variation in the RNASEH2A gene. Individuals with variants in RNASEH2A can present with a variety of phenotypes, including Aicardi-Goutieres syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"type 1 interferonopathy","termid":"MONDO:0700264"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02039":null},"genotype_count":0,"is_obsolete":false,"name":"RNASEH2A-related type 1 interferonopathy","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0700259","terms_by_termid":{"MONDO:0012472":null},"xrefs":{"Monarch":{"xref_id":"0700259"}}}


id: GO:0097520
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A multiprotein complex involved in damage recognition, DNA helix unwinding, and endonucleolytic cleavage at the site of DNA damage.","definition_xrefs":["GOC:cjm","PMID:10197977","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex","termid":"GO:0032993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"nucleotide-excision repair, preincision complex","synonyms":[{"name":"UvrA(2)-UvrB(2) complex","type":"narrow"},{"name":"UvrA(2)B(2) complex","type":"narrow"},{"name":"UvrB dimer","type":"narrow"}],"termid":"GO:0097520"}


id: PBO:0077187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toll like receptor 10","termid":"PBO:0077187"}


id: GO:0140608
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases the activity of a cysteine-type endopeptidase.","definition_xrefs":["PMID:32558991"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endopeptidase activator activity","termid":"GO:0061133"},{"relation_name":"positively_regulates","term_name":"cysteine-type endopeptidase activity","termid":"GO:0004197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"positively_regulates","termid":"GO:0008233"},{"rel_name":"regulates","termid":"GO:0016787"},{"rel_name":"regulates","termid":"GO:0003824"},{"rel_name":"regulates","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"positively_regulates","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"positively_regulates","termid":"GO:0003824"},{"rel_name":"regulates","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003674","GO:0140096","GO:0003824","GO:0008233","GO:0098772","GO:0016787","GO:0030234","GO:0140677"],"is_obsolete":false,"name":"cysteine-type endopeptidase activator activity","synonyms":[{"name":"caspase activator activator activity","type":"narrow"}],"termid":"GO:0140608"}


id: MONDO:0009821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Generalized osteosclerosis with periosteal bone formation, characteristic facial dysmorphism, brain abnormalities including intracerebral calcifications, and neonatal lethal course.","definition_xrefs":["Orphanet:1832"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal osteosclerotic dysplasia","termid":"MONDO:0019702"}],"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":"lethal osteosclerotic bone dysplasia","secondary_identifiers":["MEDGEN:342416","MESH:C535282","OMIM:259660","MESH:C564916","GARD:282","icd11.foundation:1306493470","UMLS:C1850106","OMIM:259775"],"synonyms":[{"name":"RAINE syndrome","type":"exact"},{"name":"RNS","type":"related"},{"name":"Raine syndrome","type":"exact"},{"name":"combination of microcephaly, exophthalmos, hypoplastic nose and midface, gum hyperplasia, cleft palate, apparently low-set ears, and osteosclerosis","type":"related"},{"name":"lethal osteosclerotic bone dysplasia","type":"exact"},{"name":"osteomalacia, sclerosing, with cerebral calcification","type":"exact"},{"name":"osteosclerotic bone dysplasia, lethal","type":"exact"}],"termid":"MONDO:0009821","xrefs":{"Monarch":{"xref_id":"0009821"}}}


id: MONDO:0015839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"uterine disorder","termid":"MONDO:0002654"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septate uterus","secondary_identifiers":["UMLS:C0152240","SCTID:22504001","MEDGEN:56272","icd11.foundation:1959106408","MedDRA:10062606","GARD:20180","Orphanet:180122"],"termid":"MONDO:0015839","xrefs":{"Monarch":{"xref_id":"0015839"}}}


id: GO:2000034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of seed maturation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of seed development","termid":"GO:0080050"},{"relation_name":"regulates","term_name":"seed maturation","termid":"GO:0010431"}],"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 seed maturation","termid":"GO:2000034"}


id: RO:0002244
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Any relationship between an exposure event or process and any other entity.","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_related_to","termid":"RO:0002410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"related_via_exposure_to","termid":"RO:0002244"}


id: MONDO:0008290
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"porokeratosis of Mibelli","termid":"MONDO:0019141"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"porokeratosis 1, Mibelli type","secondary_identifiers":["GARD:15108","OMIM:175800"],"synonyms":[{"name":"POROK1","type":"exact"},{"name":"porokeratosis 1, MIBELLI type","type":"related"},{"name":"porokeratosis 1, multiple types","type":"related"},{"name":"porokeratosis of Mibelli","type":"related"}],"termid":"MONDO:0008290","xrefs":{"Monarch":{"xref_id":"0008290"}}}


id: PBO:0071779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein lateral stalk subunit P0 pseudogene 7","termid":"PBO:0071779"}


id: MONDO:0006637
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute renal failure caused by the cell death of the renal tubules. Causes include nephrotoxins, cytotoxic drugs, and antibiotics.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute kidney failure","termid":"MONDO:0002492"}],"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":"acute kidney tubular necrosis","secondary_identifiers":["HP:0008682","MedDRA:10023441","MESH:D007683","ICD9:584.5","EFO:1000794","SCTID:35455006","SCTID:23697004","MEDGEN:7213","NCIT:C34749","DOID:12556","UMLS:C0022672"],"synonyms":[{"name":"ATN - acute tubular necrosis","type":"exact"},{"name":"acute renal failure with lesion of tubular necrosis","type":"exact"},{"name":"acute renal failure with tubular necrosis","type":"exact"},{"name":"acute tubular necrosis","type":"exact"},{"name":"acute tubule necrosis","type":"exact"}],"termid":"MONDO:0006637","xrefs":{"Monarch":{"xref_id":"0006637"}}}


id: PBO:0075634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small proline rich protein 2D","termid":"PBO:0075634"}


id: GO:0090152
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a protein to a specific location in the mitochondrial membrane that contributes to mitochondrial fission.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of protein localization to mitochondrial membrane","termid":"GO:0090151"},{"relation_name":"part_of","term_name":"mitochondrial fission","termid":"GO:0000266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0007005"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0007005","GO:0061024"],"is_obsolete":false,"name":"establishment of protein localization to mitochondrial membrane involved in mitochondrial fission","synonyms":[{"name":"establishment of protein localisation in mitochondrial membrane involved in mitochondrial fission","type":"exact"},{"name":"establishment of protein localization in mitochondrial membrane involved in mitochondrial fission","type":"exact"}],"termid":"GO:0090152"}


id: PBO:0084274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Integral membrane protein; required for the biogenesis of ER-derived COPII transport vesicles; interacts with Yif1p and Yos1p; localizes to the Golgi, the ER, and COPII vesicles; human homolog YIPF5 can complement yeast yip1 mutant","termid":"PBO:0084274"}


id: GO:0106145
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalyzes of the reaction: scopoletin + 2-oxoglutarate+O2=fraxetin +succinate+ CO2).","definition_xrefs":["GOC:lr","RHEA:57848","PMID:29581584","PMID:29361149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"scopoletin 8-hydroxylase activity","secondary_identifiers":["EC:1.14.11.60"],"termid":"GO:0106145"}


id: MONDO:0007539
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":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"Mendelian encephalopathy","termid":"MONDO:0100198"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encephalopathy, recurrent, of childhood","secondary_identifiers":["GARD:3949","MEDGEN:342069","MESH:C536407","Orphanet:2672","OMIM:130950","UMLS:C1851708"],"synonyms":[{"name":"Neuhauser Eichner Opitz syndrome","type":"related"},{"name":"encephalopathy recurrent of childhood","type":"exact"},{"name":"encephalopathy, recurrent, of childhood","type":"exact"}],"termid":"MONDO:0007539","xrefs":{"Monarch":{"xref_id":"0007539"}}}


id: PBO:0068101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 408","termid":"PBO:0068101"}


id: GO:0048700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a seed acquires tolerance to severe drying, before entering into a dry, either dormant or quiescent state.","definition_xrefs":["GOC:ki","ISBN:9781405139830","GOC:PO_curators","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"acquisition of desiccation tolerance","termid":"GO:0097439"},{"relation_name":"part_of","term_name":"seed dormancy process","termid":"GO:0010162"}],"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":"acquisition of desiccation tolerance in seed","synonyms":[{"name":"acquisition of desiccation tolerance","type":"broad"}],"termid":"GO:0048700"}


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: GO:2000522
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of immunological synapse formation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"regulation of immunological synapse formation","termid":"GO:2000520"},{"relation_name":"positively_regulates","term_name":"immunological synapse formation","termid":"GO:0001771"}],"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 immunological synapse formation","synonyms":[{"name":"positive regulation of formation of immunological synapse","type":"exact"}],"termid":"GO:2000522"}


id: PATO:0001423
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A reflectivity quality inhering in the bearer by virtue of the bearer's ability to refract light.","definition_xrefs":["biology-online:biology-online"],"direct_ancestors":[{"relation_name":"is_a","term_name":"refractivity","termid":"PATO:0001372"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"refractile","termid":"PATO:0001423"}


id: FYPO:0006368
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 heterochromatin is assembled over a normal (i.e. indistinguishable from wild type) portion of the centromeric region of the chromosome.","definition_xrefs":["PMID:29214404","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal chromatin organization","termid":"FYPO:0007940"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal spatial extent of centromeric heterochromatin assembly","synonyms":[{"name":"normal spatial extent of centromeric heterochromatin assembly during mitotic cell cycle","type":"related"},{"name":"normal spatial extent of centromeric heterochromatin assembly during vegetative growth","type":"exact"},{"name":"normal spatial extent of centromeric heterochromatin formation","type":"exact"}],"termid":"FYPO:0006368"}


id: MONDO:1011719
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intestinal cobalamin (vitamin B12) malabsorption, non-human animal","secondary_identifiers":["OMIA:001791"],"termid":"MONDO:1011719","xrefs":{"Monarch":{"xref_id":"1011719"}}}


id: GO:0102499
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: hydrogenphosphate + a plant soluble heteroglycan = alpha-D-glucose 1-phosphate + a plant soluble heteroglycan.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete SHG alpha-glucan phosphorylase activity (obsolete GO:0102499)","termid":"GO:0102499"}


id: GO:0007247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Upregulation of MAP kinase activity in the context of transduction of mating pheromone signal, as described for Saccharomyces.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of MAPK (mating sensu Saccharomyces) (obsolete GO:0007247)","synonyms":[{"name":"activation of MAPK (mating sensu Saccharomyces)","type":"exact"}],"termid":"GO:0007247"}


id: PBO:0005768
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex subunit Sgf73","termid":"PBO:0005768"}


id: PBO:0060078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 25","termid":"PBO:0060078"}


id: GO:0044237
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways by which individual cells transform chemical substances.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular metabolic process (obsolete GO:0044237)","secondary_identifiers":["Reactome:R-HSA-1428517"],"synonyms":[{"name":"cellular metabolism","type":"exact"},{"name":"intermediary metabolism","type":"related"}],"termid":"GO:0044237"}


id: GO:0070009
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a single N-terminal amino acid residue from a polypeptide chain by a catalytic mechanism that involves a catalytic triad consisting of a serine nucleophile that is activated by a proton relay involving an acidic residue (e.g. aspartate or glutamate) and a basic residue (usually histidine).","direct_ancestors":[{"relation_name":"is_a","term_name":"aminopeptidase activity","termid":"GO:0004177"},{"relation_name":"is_a","term_name":"serine-type exopeptidase activity","termid":"GO:0070008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0008233","GO:0003824","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"serine-type aminopeptidase activity","termid":"GO:0070009"}


id: PBO:0082942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic GTPase-activating protein; activates Ypt/Rab transport GTPases Ypt6p, Ypt31p and Sec4p; involved in recycling of internalized proteins and regulation of Golgi secretory function","termid":"PBO:0082942"}


id: PBO:0047855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, 5-azacytidine type, common, fra(1)(q42)","termid":"PBO:0047855"}


id: GO:0016573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a histone by the addition of an acetyl group.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete histone acetylation (obsolete GO:0016573)","termid":"GO:0016573"}


id: MONDO:0008167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cystic teratoma that arises from the ovary. It presents as a cystic mass that contains sebaceous material admixed with hairs. In a minority of cases it is bilateral.","definition_xrefs":["NCIT:C3856"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermoid cyst","termid":"MONDO:0002378"},{"relation_name":"is_a","term_name":"ovarian cystic teratoma","termid":"MONDO:0003281"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dermoid cyst of ovary","secondary_identifiers":["DOID:5117","icd11.foundation:1067463359","MEDGEN:68637","OMIM:166950","UMLS:C0237020","MESH:C562731"],"synonyms":[{"name":"dermoid cyst (& [ovarian])","type":"exact"},{"name":"dermoid cyst of ovary","type":"exact"},{"name":"dermoid cyst of the ovary","type":"exact"},{"name":"dermoid cyst, ovarian","type":"related"},{"name":"ovarian dermoid cyst","type":"exact"},{"name":"ovary dermoid cyst","type":"exact"},{"name":"teratoma, ovarian","type":"related"}],"termid":"MONDO:0008167","xrefs":{"Monarch":{"xref_id":"0008167"}}}


id: GO:1903396
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of secondary cell septum biogenesis.","definition_xrefs":["GOC:di","GO_REF:0000058","GOC:TermGenie","PMID:23878277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mitotic division septum assembly","termid":"GO:0140280"},{"relation_name":"is_a","term_name":"regulation of secondary cell septum biogenesis","termid":"GO:1903395"},{"relation_name":"negatively_regulates","term_name":"secondary cell septum biogenesis","termid":"GO:1990344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0000281"},{"rel_name":"negatively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0000281"}],"interesting_parent_ids":["GO:0008150","GO:0007049","GO:0000281","GO:0044085"],"is_obsolete":false,"name":"negative regulation of secondary cell septum biogenesis","synonyms":[{"name":"down regulation of secondary cell septum biogenesis","type":"exact"},{"name":"down-regulation of secondary cell septum biogenesis","type":"exact"},{"name":"downregulation of secondary cell septum biogenesis","type":"exact"},{"name":"inhibition of secondary cell septum biogenesis","type":"narrow"}],"termid":"GO:1903396"}


id: GO:0015174
data:
  {"annotated_genes":["SJAG_00051","SJAG_00877","SJAG_02029","SJAG_04787","SJAG_04637","SJAG_03256","SJAG_03400","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90738,94930,96033],"is_not":false,"summary":null,"term":"GO:0015174"},{"annotations":[97687,100683,79473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061459"},{"annotations":[97688,79466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005290"},{"annotations":[110340,97689,103120,79470,100684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015189"}]},"cv_name":"molecular_function","definition":"Enables the transfer of basic amino acids from one side of a membrane to the other. Basic amino acids have side chains with a positive charge at pH 7.3.","definition_xrefs":["ISBN:0815340729","GOC:ai","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid transmembrane transporter activity","termid":"GO:0015171"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00051":null,"SJAG_00877":null,"SJAG_02029":null,"SJAG_03256":null,"SJAG_03400":null,"SJAG_04637":null,"SJAG_04725":null,"SJAG_04787":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"basic amino acid transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0005286","Reactome:R-HSA-8932851","Reactome:R-HSA-8959781","GO:0015326"],"synonyms":[{"name":"basic amino acid permease activity","type":"exact"},{"name":"basic amino acid transporter activity","type":"broad"},{"name":"cationic amino acid transmembrane transporter activity","type":"related"}],"termid":"GO:0015174","terms_by_termid":{"GO:0005290":null,"GO:0015174":null,"GO:0015189":null,"GO:0061459":null}}


id: MONDO:0006646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, slow-growing neoplasm that arises from the dermis or subcutaneous tissue. It is characterized by the presence of well-differentiated smooth muscle cells which are arranged around numerous vessels.","definition_xrefs":["NCIT:C3747"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"benign perivascular tumor","termid":"MONDO:0003342"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angioleiomyoma","secondary_identifiers":["DOID:4265","MESH:D018229","UMLS:C0206653","EFO:1000084","ICDO:8894/0","MEDGEN:60202"],"synonyms":[{"name":"angioleiomyoma","type":"exact"},{"name":"angiomyoma","type":"exact"},{"name":"angiomyoma (morphologic abnormality)","type":"exact"},{"name":"vascular leiomyoma","type":"exact"}],"termid":"MONDO:0006646","xrefs":{"Monarch":{"xref_id":"0006646"}}}


id: GO:0047298
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-amino-2-methylpropanoate + 2-oxoglutarate = 2-methyl-3-oxopropanoate + L-glutamate.","definition_xrefs":["EC:2.6.1.22","RHEA:13993"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016769"}],"interesting_parent_ids":["GO:0003674","GO:0016769","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"(S)-3-amino-2-methylpropionate transaminase activity","secondary_identifiers":["KEGG_REACTION:R04188","MetaCyc:2.6.1.22-RXN"],"synonyms":[{"name":"(S)-3-amino-2-methylpropanoate:2-oxoglutarate aminotransferase activity","type":"related"},{"name":"(S)-3-amino-2-methylpropionate aminotransferase activity","type":"exact"},{"name":"L-3-aminoisobutyrate aminotransferase activity","type":"related"},{"name":"L-3-aminoisobutyrate transaminase activity","type":"related"},{"name":"L-3-aminoisobutyric aminotransferase activity","type":"related"},{"name":"L-AIBAT activity","type":"related"},{"name":"beta-aminobutyric transaminase activity","type":"related"},{"name":"beta-aminoisobutyrate-alpha-ketoglutarate transaminase activity","type":"related"}],"termid":"GO:0047298"}


id: MONDO:0013701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MRT32 (obsolete MONDO:0013701)","secondary_identifiers":["OMIM:614339"],"termid":"MONDO:0013701","xrefs":{"Monarch":{"xref_id":"0013701"}}}


id: PBO:0059823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metadherin pseudogene 3","termid":"PBO:0059823"}


id: PBO:0061420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptide Y receptor Y4-2","termid":"PBO:0061420"}


id: PBO:0068498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 83, pseudogene","termid":"PBO:0068498"}


id: PBO:0070704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 8","termid":"PBO:0070704"}


id: PBO:0084738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial intermembrane space protein; forms complex with Ups2p that transfers phosphatidylserine from outer membrane to inner membrane for phosphatidylethanolamine synthesis; mutation affects mitochondrial distribution and morphology; contains twin cysteine-x9-cysteine motifs; protein abundance increases in response to DNA replication stress","termid":"PBO:0084738"}


id: MONDO:0000569
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hypersensitivity reaction type II disease that involves the endocrine system.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"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":"autoimmune disorder of endocrine system","secondary_identifiers":["UMLS:C0342552","SCTID:237822008","MEDGEN:575099","ICD9:279.49","DOID:0060005"],"synonyms":[{"name":"endocrine system autoimmune disease","type":"exact"},{"name":"endocrine system hypersensitivity reaction type II disease","type":"exact"}],"termid":"MONDO:0000569","xrefs":{"Monarch":{"xref_id":"0000569"}}}


id: PBO:0085886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; involved in invasive and pseudohyphal growth; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm in a punctate pattern","termid":"PBO:0085886"}


id: GO:1905214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of RNA binding.","definition_xrefs":["GOC:PARL","GOC:TermGenie","GO_REF:0000059","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of RNA binding (obsolete GO:1905214)","termid":"GO:1905214"}


id: PBO:0077239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane and coiled-coil domains 1","termid":"PBO:0077239"}


id: FYPO:0004683
data:
  {"alleles_by_uniquename":{"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119777,119887],"is_not":false,"summary":null,"term":"FYPO:0004683"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the nucleolus is partitioned to daughter cells unequally during cell division.","definition_xrefs":["PomBase:mah","PMID:16478992","PMID:1661641"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process phenotype during vegetative growth","termid":"FYPO:0001331"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03449":null,"SJAG_03575":null},"genotype_count":2,"genotypes_by_uniquename":{"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"apc2-361(E548K ts)","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"unequal nucleolus inheritance","references_by_uniquename":{"PMID:23786411":null,"PMID:24184107":null},"single_locus_annotated_genes":["SJAG_03449","SJAG_03575"],"single_locus_genotype_uniquenames":["man1delta","apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"unequal mitotic nucleolar partitioning","type":"exact"},{"name":"unequal mitotic nucleolar segregation","type":"exact"},{"name":"unequal nucleolar inheritance","type":"exact"},{"name":"unequal nucleolus distribution","type":"exact"},{"name":"unequal nucleolus inheritance during mitotic cell cycle","type":"related"},{"name":"unequal nucleolus inheritance during vegetative growth","type":"exact"},{"name":"unequal nucleolus partitioning","type":"exact"},{"name":"unequal nucleolus segregation","type":"exact"},{"name":"unequal rDNA segregation","type":"related"}],"termid":"FYPO:0004683","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000137":null,"FYPO:0004683":null}}


id: GO:0060568
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of peptide hormone processing. Peptide hormone processing is the generation of a mature peptide hormone by posttranslational processing of a prohormone.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hormone metabolic process","termid":"GO:0032350"},{"relation_name":"is_a","term_name":"regulation of amide metabolic process","termid":"GO:0034248"},{"relation_name":"is_a","term_name":"regulation of protein processing","termid":"GO:0070613"},{"relation_name":"regulates","term_name":"peptide hormone processing","termid":"GO:0016486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0051604"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051604","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of peptide hormone processing","termid":"GO:0060568"}


id: GO:2001157
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of proline catabolic process to glutamate.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of amine catabolic process","termid":"GO:0033242"},{"relation_name":"is_a","term_name":"negative regulation of glutamate metabolic process","termid":"GO:2000212"},{"relation_name":"is_a","term_name":"negative regulation of proline metabolic process","termid":"GO:2000215"},{"relation_name":"is_a","term_name":"regulation of proline catabolic process to glutamate","termid":"GO:2001156"},{"relation_name":"negatively_regulates","term_name":"proline catabolic process to glutamate","termid":"GO:0010133"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"negative regulation of proline catabolic process to glutamate","synonyms":[{"name":"negative regulation of proline breakdown to glutamate","type":"exact"},{"name":"negative regulation of proline degradation to glutamate","type":"exact"},{"name":"negative regulation of proline oxidation","type":"related"}],"termid":"GO:2001157"}


id: PBO:0016059
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae RAT1","termid":"PBO:0016059"}


id: MONDO:0005698
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A clinical diagnosis presenting with painless cervical dilatation and spontaneous mid-trimester birth in recurrent pregnancies in the absence of spontaneous membrane rupture, bleeding or clinical chorioamnionitis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervix disorder","termid":"MONDO:0002256"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical incompetence","secondary_identifiers":["EFO:0007202","SCTID:17382005","ICD9:622.5","UMLS:C0007871","ICD9:654.50","MESH:D002581","DOID:9681","MEDGEN:2972"],"termid":"MONDO:0005698","xrefs":{"Monarch":{"xref_id":"0005698"}}}


id: PBO:0068388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 207","termid":"PBO:0068388"}


id: GO:0072369
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of lipid transport by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:BHF","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of lipid transport by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:0072369)","synonyms":[{"name":"regulation of lipid transport by positive regulation of transcription from an RNA polymerase II promoter","type":"exact"}],"termid":"GO:0072369"}


id: PBO:0006175
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_input","termid":"PBO:0006175"}


id: PBO:0049671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxyacyl-CoA dehydratase 3","termid":"PBO:0049671"}


id: FYPO:0002300
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A mixed population phenotype in which all cells in a population are inviable, and the population includes a mixture of germinated spores with elongated germ tubes and elongated vegetative cells. The elongated cells arise from division of some of the germinated spores, and may form a microcolony of up to 64 cells.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable mixed population including germinated spores with elongated germ tubes and elongated cells (obsolete FYPO:0002300)","synonyms":[{"name":"inviable mixed population including germinated spores with elongated germ tubes and long cells","type":"exact"}],"termid":"FYPO:0002300"}


id: MONDO:0008097
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86236],"is_not":false,"summary":null,"term":"MONDO:0008097"}]},"cv_name":"mondo","definition":"Linear nevus sebaceous syndrome (LNSS) is characterized by the association of a large sebaceous nevus, usually appearing on the face or on the scalp, with a broad spectrum of abnormalities that may affect every organ system, including the central nervous system (brain neoplasms, hemimegalencephaly and lateral ventricle enlargement).","definition_xrefs":["Orphanet:2612"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hamartoma","termid":"MONDO:0006499"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"is_a","term_name":"palpebral nevus","termid":"MONDO:0020179"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"linear nevus sebaceous syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4552097","DOID:0111530","OMIM:163200","NCIT:C4678","MEDGEN:1646345","GARD:10291","NORD:1692"],"synonyms":[{"name":"Epidermal Nevus syndrome, formerly","type":"related"},{"name":"JNP","type":"related"},{"name":"Jadassohn Nevus phakomatosis","type":"related"},{"name":"Jadassohn nevus phakomatosis","type":"related"},{"name":"Nevus Sebaceus Syndrome","type":"exact"},{"name":"Nevus sebaceous of Jadassohn","type":"exact"},{"name":"Nevus sebaceus of Jadassohn","type":"exact"},{"name":"Nevus sebaceus syndrome","type":"exact"},{"name":"SCHIMMELPENNING-FEUERSTEIN-MIMS syndrome","type":"related"},{"name":"SFM","type":"related"},{"name":"SFM syndrome","type":"related"},{"name":"Schimmelpenning Feuerstein Mims syndrome","type":"related"},{"name":"Schimmelpenning syndrome","type":"exact"},{"name":"Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic","type":"exact"},{"name":"Sfm syndrome","type":"related"},{"name":"Solomon syndrome","type":"exact"},{"name":"epidermal nevus syndrome","type":"related"},{"name":"linear sebaceous Nevus","type":"exact"},{"name":"linear sebaceous Nevus syndrome","type":"related"},{"name":"organoid Nevus","type":"exact"},{"name":"organoid Nevus phakomatosis","type":"related"},{"name":"organoid nevus phakomatosis","type":"related"},{"name":"organoid nevus syndrome","type":"exact"},{"name":"sebaceous Nevus syndrome, linear","type":"related"},{"name":"sebaceous nevus syndrome linear","type":"related"}],"termid":"MONDO:0008097","terms_by_termid":{"MONDO:0008097":null},"xrefs":{"Monarch":{"xref_id":"0008097"}}}


id: PBO:0045074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLG associated protein 2","termid":"PBO:0045074"}


id: PBO:0054684
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 2092","termid":"PBO:0054684"}


id: PBO:0053325
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 114","termid":"PBO:0053325"}


id: GO:0046605
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the centrosome cycle, the processes of centrosome duplication and separation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of microtubule-based process","termid":"GO:0032886"},{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"centrosome cycle","termid":"GO:0007098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of centrosome cycle","termid":"GO:0046605"}


id: PBO:0042518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 1","termid":"PBO:0042518"}


id: PBO:0077838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPBGL antisense RNA 1","termid":"PBO:0077838"}


id: GO:0051330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle 'gap' phase which is the interval between the completion of DNA segregation by meiosis and the beginning of DNA synthesis.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G1 phase","termid":"GO:0051318"},{"relation_name":"part_of","term_name":"meiotic interphase","termid":"GO:0051328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0051328"}],"interesting_parent_ids":["GO:0008150","GO:0051328"],"is_obsolete":false,"name":"meiotic G1 phase","synonyms":[{"name":"G1 phase of meiotic cell cycle","type":"exact"}],"termid":"GO:0051330"}


id: PBO:0057295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 512-2","termid":"PBO:0057295"}


id: PBO:0034181
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-results_in_developmental_regression_of","termid":"PBO:0034181"}


id: PBO:0068499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 84, pseudogene","termid":"PBO:0068499"}


id: FYPO:0001001
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the mitotic cell cycle is arrested at the mitotic G2/M phase transition, instead of the normal G1 phase, when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah","PMID:19366728"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle arrest in response to nitrogen starvation","termid":"FYPO:0000710"},{"relation_name":"is_a","term_name":"cell cycle arrest at mitotic G2/M phase transition during starvation","termid":"FYPO:0001151"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000631","FYPO:0000002","FYPO:0000298"],"is_obsolete":false,"name":"abnormal cell cycle arrest at mitotic G2/M phase transition during nitrogen starvation","synonyms":[{"name":"abnormal cell cycle arrest at mitotic G2/M phase transition during nitrogen depletion","type":"exact"},{"name":"abnormal cell cycle arrest at mitotic G2/M phase transition during nitrogen deprivation","type":"exact"},{"name":"abnormal cell cycle arrest in mitotic G2 phase during nitrogen starvation","type":"related"},{"name":"abnormal mitotic cell cycle arrest at mitotic G2/M phase transition during nitrogen starvation","type":"exact"},{"name":"abolished mitotic G2/M phase transition during nitrogen starvation","type":"related"},{"name":"advanced nitrogen deprivation-induced G1 arrest","type":"related"},{"name":"cell cycle arrest at mitotic G2/M phase transition during nitrogen starvation","type":"exact"},{"name":"mitotic G2/M phase transition arrest during nitrogen starvation","type":"exact"}],"termid":"FYPO:0001001"}


id: PBO:0048541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GET1-SH3BGR readthrough","termid":"PBO:0048541"}


id: FYPO:0000987
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular response phenotype in which pheromone-responsive positive regulation of transcription from an RNA polymerase II promoter results in a lower-than-normal level of transcription at a given pheromone level.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete decreased transcriptional response to pheromone at normal pheromone level (obsolete FYPO:0000987)","synonyms":[{"name":"decreased positive regulation of transcription from RNA polymerase II promoter by pheromones at normal pheromone level","type":"exact"},{"name":"decreased sensitivity of positive regulation of transcription from RNA polymerase II promoter by pheromones to pheromone","type":"related"},{"name":"decreased transcriptional response to pheromone","type":"related"},{"name":"reduced transcriptional response to pheromone at normal pheromone level","type":"exact"},{"name":"resistant to pheromone","type":"related"}],"termid":"FYPO:0000987"}


id: GO:0044320
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a leptin stimulus. Leptin is a hormone manufactured primarily in the adipocytes of white adipose tissue, and the level of circulating leptin is directly proportional to the total amount of fat in the body. It plays a key role in regulating energy intake and energy expenditure, including appetite and metabolism.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to hormone stimulus","termid":"GO:0032870"},{"relation_name":"is_a","term_name":"response to leptin","termid":"GO:0044321"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to leptin stimulus","termid":"GO:0044320"}


id: MONDO:0016522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11.","definition_xrefs":["Orphanet:2351"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kousseff syndrome","secondary_identifiers":["SCTID:726083008","MESH:C537223","GARD:4752","MEDGEN:444057","UMLS:C2931444"],"synonyms":[{"name":"sacral meningocele conotruncal heart defects","type":"related"},{"name":"sacral meningocele, conotruncal heart defects, and minor anomalies of head and neck","type":"related"},{"name":"sacral meningocele-conotruncal heart defects syndrome","type":"exact"}],"termid":"MONDO:0016522","xrefs":{"Monarch":{"xref_id":"0016522"}}}


id: GO:0009972
data:
  {"annotated_genes":["SJAG_03771","SJAG_01673"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70176,70274],"is_not":false,"summary":null,"term":"GO:0009972"}]},"cv_name":"biological_process","definition":"The removal of amino group in the presence of water.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytidine catabolic process","termid":"GO:0006216"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01673":null,"SJAG_03771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"cytidine deamination","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0009972","terms_by_termid":{"GO:0009972":null}}


id: PBO:0090066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snRNP binding protein Sgt1","termid":"PBO:0090066"}


id: MONDO:0014438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the BBS10 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bardet-Biedl syndrome","termid":"MONDO:0015229"},{"relation_name":"is_a","term_name":"BBS10-related ciliopathy","termid":"MONDO:0700237"}],"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 10","secondary_identifiers":["OMIM:615987","UMLS:C1859568","MEDGEN:347909","MESH:C565919","DOID:0110132","GARD:10209"],"synonyms":[{"name":"BBS10","type":"exact"},{"name":"BBS10 Bardet-Biedl syndrome","type":"exact"},{"name":"Bardet-Biedl syndrome 10","type":"exact"},{"name":"Bardet-Biedl syndrome caused by mutation in BBS10","type":"exact"},{"name":"Bardet-Biedl syndrome type 10","type":"exact"}],"termid":"MONDO:0014438","xrefs":{"Monarch":{"xref_id":"0014438"}}}


id: MOD:00113
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-geranylgeranyl-L-cysteine.","definition_xrefs":["PubMed:15609361","DeltaMass:0","OMSSA:49","PubMed:1483450","RESID:AA0104","Unimod:48#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"geranylgeranylated residue","termid":"MOD:00441"},{"relation_name":"is_a","term_name":"isoprenylated cysteine","termid":"MOD:01110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"},{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905","MOD:01155"],"is_obsolete":false,"name":"S-geranylgeranyl-L-cysteine","synonyms":[{"name":"(2R)-2-amino-3-([(2E,6E,10Z)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]sulfanyl)propanoic acid","type":"exact"},{"name":"2-amino-3-(3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenylthio)propanoic acid","type":"exact"},{"name":"Geranyl-geranyl","type":"related"},{"name":"GeranylGeranyl","type":"related"},{"name":"LIPID S-geranylgeranyl cysteine","type":"exact"},{"name":"S-geranylgeranyl","type":"exact"},{"name":"S-geranylgeranyl-L-cysteine","type":"exact"},{"name":"SGergerCys","type":"exact"},{"name":"geranylgeranylc","type":"exact"}],"termid":"MOD:00113"}


id: MONDO:0003757
data:
  {"annotated_genes":["SJAG_00773","SJAG_03457","SJAG_05289","SJAG_02615","SJAG_04757","SJAG_01857","SJAG_04628","SJAG_04123","SJAG_03320","SJAG_00660","SJAG_04566","SJAG_04325","SJAG_02322","SJAG_04913","SJAG_01537","SJAG_01854","SJAG_00199","SJAG_01530","SJAG_02306","SJAG_01848","SJAG_03866","SJAG_04145","SJAG_04110","SJAG_04292","SJAG_00564","SJAG_00308","SJAG_01159","SJAG_04537","SJAG_04506","SJAG_03895"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85371,85372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014702"},{"annotations":[87342,87341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014975"},{"annotations":[87608],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030669"},{"annotations":[85790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014567"},{"annotations":[86005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009748"},{"annotations":[86058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011489"},{"annotations":[87410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011532"},{"annotations":[85531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010043"},{"annotations":[85536,85534,85535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012256"},{"annotations":[85421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012476"},{"annotations":[85541],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012453"},{"annotations":[87393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012866"},{"annotations":[86663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012787"},{"annotations":[86852,86851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008438"},{"annotations":[87111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012928"},{"annotations":[85638,85639,85637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014018"},{"annotations":[85636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014020"},{"annotations":[85997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014305"},{"annotations":[85981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014282"},{"annotations":[85468],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014644"},{"annotations":[86471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014882"},{"annotations":[86843,86842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011006"},{"annotations":[85452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014679"},{"annotations":[87096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012651"},{"annotations":[86882],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957221"},{"annotations":[86392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957958"},{"annotations":[87050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032906"},{"annotations":[86394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030482"},{"annotations":[86438],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030512"},{"annotations":[87190,87189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031019"},{"annotations":[86687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957308"},{"annotations":[86688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957309"}]},"cv_name":"mondo","definition":"Complete paralysis of the lower half of the body including both legs, often caused by damage to the spinal cord.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"central nervous system disorder","termid":"MONDO:0002602"},{"relation_name":"is_a","term_name":"palsy","termid":"MONDO:0006496"}],"gene_count":30,"genes_by_uniquename":{"SJAG_00199":null,"SJAG_00308":null,"SJAG_00564":null,"SJAG_00660":null,"SJAG_00773":null,"SJAG_01159":null,"SJAG_01530":null,"SJAG_01537":null,"SJAG_01848":null,"SJAG_01854":null,"SJAG_01857":null,"SJAG_02306":null,"SJAG_02322":null,"SJAG_02615":null,"SJAG_03320":null,"SJAG_03457":null,"SJAG_03866":null,"SJAG_03895":null,"SJAG_04110":null,"SJAG_04123":null,"SJAG_04145":null,"SJAG_04292":null,"SJAG_04325":null,"SJAG_04506":null,"SJAG_04537":null,"SJAG_04566":null,"SJAG_04628":null,"SJAG_04757":null,"SJAG_04913":null,"SJAG_05289":null},"genotype_count":0,"is_obsolete":false,"name":"paraplegia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:607","EFO:0009679","MEDGEN:45323","icd11.foundation:1212533558","UMLS:C0030486","NCIT:C50687","ICD9:344.1","MESH:D010264","SCTID:60389000"],"synonyms":[{"name":"paraplegia, lower","type":"exact"},{"name":"severe or complete loss of motor function in the lower extremities and lower portions of the trunk","type":"related"}],"termid":"MONDO:0003757","terms_by_termid":{"MONDO:0008438":null,"MONDO:0009748":null,"MONDO:0010043":null,"MONDO:0011006":null,"MONDO:0011489":null,"MONDO:0011532":null,"MONDO:0012256":null,"MONDO:0012453":null,"MONDO:0012476":null,"MONDO:0012651":null,"MONDO:0012787":null,"MONDO:0012866":null,"MONDO:0012928":null,"MONDO:0014018":null,"MONDO:0014020":null,"MONDO:0014282":null,"MONDO:0014305":null,"MONDO:0014567":null,"MONDO:0014644":null,"MONDO:0014679":null,"MONDO:0014702":null,"MONDO:0014882":null,"MONDO:0014975":null,"MONDO:0030482":null,"MONDO:0030512":null,"MONDO:0030669":null,"MONDO:0031019":null,"MONDO:0032906":null,"MONDO:0957221":null,"MONDO:0957308":null,"MONDO:0957309":null,"MONDO:0957958":null},"xrefs":{"Monarch":{"xref_id":"0003757"}}}


id: PBO:0042948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 2","termid":"PBO:0042948"}


id: GO:0000208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a MAP kinase to the nucleus during osmolarity sensing.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete MAPK import into nucleus involved in osmosensory signaling pathway (obsolete GO:0000208)","synonyms":[{"name":"MAPK import into nucleus during osmolarity sensing","type":"exact"},{"name":"MAPK import into nucleus involved in osmosensory signalling pathway","type":"exact"},{"name":"nuclear translocation of MAPK during osmolarity sensing","type":"exact"},{"name":"nuclear translocation of MAPK involved in osmosensory signaling pathway","type":"narrow"},{"name":"nuclear translocation of MAPK involved in osmosensory signalling pathway","type":"narrow"},{"name":"osmolarity sensing, MAPK import into nucleus","type":"exact"},{"name":"osmolarity sensing, nuclear translocation of MAPK","type":"narrow"}],"termid":"GO:0000208"}


id: GO:0090296
data:
  {"annotated_genes":["SJAG_03957"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090297"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of the process in which new strands of DNA are synthesized in the mitochondrion.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA-templated DNA replication","termid":"GO:0090329"},{"relation_name":"is_a","term_name":"regulation of mitochondrial DNA metabolic process","termid":"GO:1901858"},{"relation_name":"regulates","term_name":"mitochondrial DNA replication","termid":"GO:0006264"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03957":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006260"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0006260"],"is_obsolete":false,"name":"regulation of mitochondrial DNA replication","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of mitochondrial DNA synthesis","type":"related"}],"termid":"GO:0090296","terms_by_termid":{"GO:0090297":null}}


id: GO:0014877
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 muscle inactivity stimulus. This process 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 muscle inactivity","termid":"GO:0014870"},{"relation_name":"is_a","term_name":"response to stimulus involved in regulation of muscle adaptation","termid":"GO:0014874"}],"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 muscle inactivity involved in regulation of muscle adaptation","termid":"GO:0014877"}


id: _global:precedes
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"x precedes y if and only if the time point at which x ends is before or equivalent to the time point at which y starts. Formally: x precedes y iff ω(x) <= α(y), where α is a function that maps a process to a start point, and ω is a function that maps a process to an end point.","direct_ancestors":[{"relation_name":"is_a","term_name":"temporally_related_to","termid":"_global:temporally_related_to"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"precedes","secondary_identifiers":["BFO:0000063"],"termid":"_global:precedes"}


id: PBO:0044545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DAP divergent transcript","termid":"PBO:0044545"}


id: GO:0070161
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cell junction that mechanically attaches a cell (and its cytoskeleton) to neighboring cells or to the extracellular matrix.","definition_xrefs":["ISBN:0815332181"],"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":"anchoring junction","synonyms":[{"name":"anchoring cell junction","type":"exact"}],"termid":"GO:0070161"}


id: PBO:0030841
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_adenine_import","termid":"PBO:0030841"}


id: GO:0046358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of butyrate, the anion of butyric acid.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"butyrate metabolic process","termid":"GO:0019605"},{"relation_name":"is_a","term_name":"short-chain fatty acid biosynthetic process","termid":"GO:0051790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"butyrate biosynthetic process","secondary_identifiers":["GO:0043439"],"synonyms":[{"name":"butanoic acid anabolism","type":"exact"},{"name":"butanoic acid biosynthesis","type":"exact"},{"name":"butanoic acid biosynthetic process","type":"exact"},{"name":"butanoic acid formation","type":"exact"},{"name":"butanoic acid synthesis","type":"exact"},{"name":"butyrate anabolism","type":"exact"},{"name":"butyrate biosynthesis","type":"exact"},{"name":"butyrate formation","type":"exact"},{"name":"butyrate synthesis","type":"exact"}],"termid":"GO:0046358"}


id: MONDO:0800353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"congenital disorder of glycosylation, type Ibb","secondary_identifiers":["UMLS:C4693133","MEDGEN:1637983"],"synonyms":[{"name":"CDG1BB","type":"exact"}],"termid":"MONDO:0800353","xrefs":{"Monarch":{"xref_id":"0800353"}}}


id: GO:0031595
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A proteasome found in the nucleus of a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome complex","termid":"GO:0000502"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear lumen","termid":"GO:0031981"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"nuclear proteasome complex","termid":"GO:0031595"}


id: GO:0035576
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals generated as a consequence of a retinoic acid receptor binding to one of its physiological ligands that results in regions of the embryo being delineated into the area in which the pronephric kidney will develop.","definition_xrefs":["GOC:bf","PMID:16979153","PMID:19909807"],"gene_count":0,"genotype_count":0,"name":"obsolete retinoic acid receptor signaling pathway involved in pronephric field specification (obsolete GO:0035576)","synonyms":[{"name":"retinoic acid receptor signalling pathway involved in pronephric field specification","type":"exact"}],"termid":"GO:0035576"}


id: GO:0097154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a neuroblast acquires the specialized structural and functional features of a GABAergic neuron.","definition_xrefs":["GOC:kmv","PMID:11517269"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron differentiation","termid":"GO:0030182"}],"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":"GABAergic neuron differentiation","termid":"GO:0097154"}


id: PBO:0056980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 29c","termid":"PBO:0056980"}


id: MONDO:1012524
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse cystic renal dysplasia and hepatic fibrosis, non-human animal","termid":"MONDO:1011915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diffuse cystic renal dysplasia and hepatic fibrosis, dog","secondary_identifiers":["OMIA:002173-9615"],"termid":"MONDO:1012524","xrefs":{"Monarch":{"xref_id":"1012524"}}}


id: FYPO:0005222
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 histone H3 to chromatin at one or more protein-coding genes is decreased.","definition_xrefs":["PMID:23028377","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to chromatin during vegetative growth","termid":"FYPO:0000452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased histone H3 localization to chromatin at protein coding gene","synonyms":[{"name":"decreased histone H3 localisation to chromatin at protein coding gene","type":"exact"},{"name":"decreased histone H3 localization to chromatin at protein coding gene during mitotic cell cycle","type":"related"},{"name":"decreased histone H3 localization to chromatin at protein-coding gene during vegetative growth","type":"exact"},{"name":"reduced histone H3 localization to chromatin at protein coding gene","type":"exact"}],"termid":"FYPO:0005222"}


id: PBO:0083008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Daughter cell-specific secreted protein with similarity to glucanases; degrades cell wall from the daughter side causing daughter to separate from mother; localizes in birth scars; expression is repressed by cAMP","termid":"PBO:0083008"}


id: GO:0033039
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of an ion by a channel that opens when a soluble salty compound has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["PMID:36332657","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ionotropic taste receptor activity","termid":"GO:0170021"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0038023","GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"ionotropic salty taste receptor activity","termid":"GO:0033039"}


id: PBO:0058595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6727","termid":"PBO:0058595"}


id: MONDO:0014503
data:
  {"annotated_genes":["SJAG_05212"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87060],"is_not":false,"summary":null,"term":"MONDO:0014503"}]},"cv_name":"mondo","definition":"Any autosomal recessive congenital cerebellar ataxia in which the cause of the disease is a mutation in the CWF19L1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"autosomal recessive congenital cerebellar ataxia","termid":"MONDO:0020043"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05212":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive spinocerebellar ataxia 17","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080064","MEDGEN:863738","OMIM:616127","Orphanet:453521","UMLS:C4015301","GARD:17786"],"synonyms":[{"name":"CWF19L1 autosomal recessive congenital cerebellar ataxia","type":"exact"},{"name":"SCAR17","type":"exact"},{"name":"autosomal recessive cerebellar ataxia due to CWF19L1 deficiency","type":"related"},{"name":"autosomal recessive congenital cerebellar ataxia caused by mutation in CWF19L1","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia type 17","type":"exact"},{"name":"spinocerebellar ataxia autosomal recessive type 17","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 17","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive type 17","type":"exact"}],"termid":"MONDO:0014503","terms_by_termid":{"MONDO:0014503":null},"xrefs":{"Monarch":{"xref_id":"0014503"}}}


id: GO:1902675
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any ciliary basal body that is part of a left ventral flagellum found in Giardia species (trophozoite stage).","definition_xrefs":["GO_REF:0000064","GOC:TermGenie","PMID:16607022","GOC:giardia","ISBN:9780124260207","PMID:5961344"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary basal body","termid":"GO:0036064"},{"relation_name":"part_of","term_name":"left ventral flagellum","termid":"GO:0097558"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005575","GO:0015630"],"is_obsolete":false,"name":"left ventral basal body","synonyms":[{"name":"cilial basal body of left ventral cilium","type":"exact"},{"name":"cilial basal body of left ventral flagellum","type":"exact"},{"name":"ciliary basal body of left ventral cilium","type":"exact"},{"name":"ciliary basal body of left ventral flagellum","type":"exact"},{"name":"cilium basal body of left ventral cilium","type":"exact"},{"name":"cilium basal body of left ventral flagellum","type":"exact"},{"name":"left ventral flagellum ciliary basal body","type":"exact"},{"name":"microtubule basal body of left ventral cilium","type":"exact"},{"name":"microtubule basal body of left ventral flagellum","type":"exact"}],"termid":"GO:1902675"}


id: PBO:0089262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(U)-specific exoribonuclease, producing 3' uridine cyclic phosphate ends Mpn1","termid":"PBO:0089262"}


id: GO:0060113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells, acquire specialized structural and/or functional features of inner ear receptor cells. Inner ear receptor cells are mechanorecptors found in the inner ear responsible for transducing signals involved in balance and sensory perception of sound.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mechanoreceptor differentiation","termid":"GO:0042490"},{"relation_name":"part_of","term_name":"inner ear development","termid":"GO:0048839"}],"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":"inner ear receptor cell differentiation","synonyms":[{"name":"inner ear hair cell differentiation","type":"exact"}],"termid":"GO:0060113"}


id: FYPO:0001674
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of L-aminoadipate-semialdehyde dehydrogenase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal oxidoreductase activity","termid":"FYPO:0000689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0001985","FYPO:0000707","FYPO:0000661"],"is_obsolete":false,"name":"abnormal L-aminoadipate-semialdehyde dehydrogenase activity","synonyms":[{"name":"abnormal alpha-aminoadipate reductase activity","type":"exact"}],"termid":"FYPO:0001674"}


id: GO:0001554
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The lysis or structural demise of the corpus luteum. During normal luteolysis, two closely related events occur. First, there is loss of the capacity to synthesize and secrete progesterone (functional luteolysis) followed by loss of the cells that comprise the corpus luteum (structural luteolysis). Preventing luteolysis is crucial to maintain pregnancy.","definition_xrefs":["PMID:10617764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovulation cycle process","termid":"GO:0022602"},{"relation_name":"part_of","term_name":"female gonad development","termid":"GO:0008585"}],"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":"luteolysis","secondary_identifiers":["Wikipedia:Luteolysis"],"termid":"GO:0001554"}


id: PBO:0034358
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-correlated_with","termid":"PBO:0034358"}


id: GO:0046448
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving tropane alkaloids, compounds containing the 8-methyl-8-azabicyclo(3.2.1)octane ring system.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkaloid metabolic process","termid":"GO:0009820"}],"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":"tropane alkaloid metabolic process","synonyms":[{"name":"tropane alkaloid metabolism","type":"exact"}],"termid":"GO:0046448"}


id: GO:1903807
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of L-threonine from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:23895341","GO_REF:0000075","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"threonine transport","termid":"GO:0015826"},{"relation_name":"is_a","term_name":"amino acid import across plasma membrane","termid":"GO:0089718"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"L-threonine import across plasma membrane","secondary_identifiers":["GO:0036231"],"synonyms":[{"name":"L-threonine import","type":"broad"},{"name":"L-threonine import into cell","type":"exact"},{"name":"L-threonine uptake","type":"exact"}],"termid":"GO:1903807"}


id: PR:O43091
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A decaprenyl-diphosphate synthase subunit 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02552"],"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":"decaprenyl-diphosphate synthase subunit 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBPJ4664.01","secondary_identifiers":["UniProtKB:O43091"],"synonyms":[{"name":"Spom972h-PDSS1","type":"exact"},{"name":"all-trans-decaprenyl-diphosphate synthase subunit 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"decaprenyl pyrophosphate synthase subunit 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43091"}


id: PBO:0117246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sepiapterin reductase Nre1","termid":"PBO:0117246"}


id: GO:0030780
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 12-hydroxydihydrochelirubine + S-adenosyl-L-methionine(1+) = S-adenosyl-L-homocysteine + dihydromacarpine + H+.","definition_xrefs":["EC:2.1.1.120","RHEA:21092"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"12-hydroxydihydrochelirubine 12-O-methyltransferase activity","secondary_identifiers":["MetaCyc:2.1.1.120-RXN","KEGG_REACTION:R04705"],"synonyms":[{"name":"S-adenosyl-L-methionine:12-hydroxydihydrochelirubine 12-O-methyltransferase activity","type":"related"}],"termid":"GO:0030780"}


id: PBO:0077497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 216","termid":"PBO:0077497"}


id: PBO:0081873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 815, pseudogene","termid":"PBO:0081873"}


id: MONDO:0000990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of subendocardial myocardial infarction.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"subendocardial myocardial infarction","termid":"MONDO:0003674"},{"relation_name":"is_a","term_name":"acute myocardial infarction","termid":"MONDO:0004781"}],"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":"acute subendocardial myocardial infarction","secondary_identifiers":["ICD9:410.7","SCTID:70422006","ICD9:410.72","ICD9:410.71","DOID:10266","ICD9:410.70","MEDGEN:538778","UMLS:C0264710"],"synonyms":[{"name":"acute nontransmural infarction","type":"related"},{"name":"acute subendocardial infarction","type":"exact"},{"name":"subendocardial infarction acute myocardial infarction","type":"related"},{"name":"subendocardial myocardial infarction, acute","type":"exact"}],"termid":"MONDO:0000990","xrefs":{"Monarch":{"xref_id":"0000990"}}}


id: PR:P0CT64
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps1601 gene.","definition_xrefs":["UniProtKB:P0CT64","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":"40S ribosomal protein S16-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18H10.14","synonyms":[{"name":"Spom972h-rps1601","type":"exact"}],"termid":"PR:P0CT64"}


id: FYPO:0001767
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 C48, C49, C60, C61 and C62 residues in a tRNA-Asp molecule, occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal tRNA methylation","termid":"FYPO:0001766"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0000294","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"decreased tRNA-Asp C48, C49, C60, C61 and C62 methylation","synonyms":[{"name":"decreased tRNA-Asp C48, C49, C60, C61 and C62 methylation during mitotic cell cycle","type":"related"},{"name":"decreased tRNA-Asp C48, C49, C60, C61 and C62 methylation during vegetative growth","type":"exact"},{"name":"decreased tRNA-Asp methylation on C48, C49, C60, C61 and C62","type":"exact"},{"name":"reduced tRNA-Asp C48, C49, C60, C61 and C62 methylation","type":"exact"}],"termid":"FYPO:0001767"}


id: PBO:0109104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF217 antisense RNA 1","termid":"PBO:0109104"}


id: PBO:0085830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to both the cytoplasm and the nucleus; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0085830"}


id: GO:0008864
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 10-formyltetrahydrofolate + H2O = (6S)-5,6,7,8-tetrahydrofolate + formate + H+.","definition_xrefs":["EC:3.5.1.10","RHEA:19833"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"formyltetrahydrofolate deformylase activity","secondary_identifiers":["KEGG_REACTION:R00944","MetaCyc:FORMYLTHFDEFORMYL-RXN"],"synonyms":[{"name":"10-formyltetrahydrofolate amidohydrolase activity","type":"related"},{"name":"formyl-FH(4) hydrolase activity","type":"related"},{"name":"formyltetrahydrofolate hydrolase activity","type":"related"}],"termid":"GO:0008864"}


id: PBO:0047053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 114 member A1","termid":"PBO:0047053"}


id: PBO:0074073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 47 pseudogene 1","termid":"PBO:0074073"}


id: MONDO:0006994
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tarsal tunnel syndrome is a nerve disorder that is characterized by pain in the ankle, foot, and toes. This condition is caused by compression of the posterior tibial nerve, which runs through a canal near the heel into the sole of the foot. When tissues around this nerve become inflamed, they can press on the nerve and cause the pain associated with tarsal tunnel syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"tibial neuropathy","termid":"MONDO:0006997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"tarsal tunnel syndrome","secondary_identifiers":["icd11.foundation:854657246","MESH:D013641","UMLS:C0039319","NCIT:C85183","EFO:1001208","GARD:7733","DOID:12526","SCTID:47374004","MedDRA:10043121","MEDGEN:52646","ICD9:355.5","ICD10CM:G57.5"],"synonyms":[{"name":"neuropathy of the posterior tibial nerve and its branches","type":"related"},{"name":"posterior tibial nerve neuralgia","type":"related"}],"termid":"MONDO:0006994","xrefs":{"Monarch":{"xref_id":"0006994"}}}


id: PBO:0048231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G antigen 2B","termid":"PBO:0048231"}


id: MONDO:0004228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypogonadotropism (obsolete MONDO:0004228)","termid":"MONDO:0004228","xrefs":{"Monarch":{"xref_id":"0004228"}}}


id: GO:0072204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the transfer of information from one cell to another and contributes to the progression of the metanephros over time, from its formation to the mature organ.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling involved in kidney development","termid":"GO:0060995"},{"relation_name":"part_of","term_name":"metanephros development","termid":"GO:0001656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"cell-cell signaling involved in metanephros development","synonyms":[{"name":"cell-cell signalling involved in metanephros development","type":"exact"}],"termid":"GO:0072204"}


id: PBO:0054777
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 2190","termid":"PBO:0054777"}


id: PBO:0088876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphopantothenate-cysteine ligase Cab2","termid":"PBO:0088876"}


id: FYPO:0003062
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which nuclear migration involved in conjugation with cellular fusion is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating","termid":"FYPO:0000031"},{"relation_name":"is_a","term_name":"abnormal nucleus positioning","termid":"FYPO:0000517"},{"relation_name":"is_a","term_name":"abnormal transport","termid":"FYPO:0001720"},{"relation_name":"is_a","term_name":"abnormal microtubule-based movement","termid":"FYPO:0007163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000301","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"abnormal nuclear congression during mating","synonyms":[{"name":"abnormal nuclear congression during karyogamy","type":"related"},{"name":"abnormal nuclear migration during mating","type":"exact"},{"name":"abnormal nuclear migration involved in conjugation with cellular fusion","type":"exact"},{"name":"abnormal nuclear movement during mating","type":"exact"},{"name":"abnormal nuclear movement during shmooing","type":"related"}],"termid":"FYPO:0003062"}


id: MONDO:0020053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete total autosomal monosomy (obsolete MONDO:0020053)","secondary_identifiers":["Orphanet:98141","icd11.foundation:599695253"],"termid":"MONDO:0020053","xrefs":{"Monarch":{"xref_id":"0020053"}}}


id: PBO:0085374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIK-related protein kinase and rapamycin target; subunit of TORC1, a complex that regulates growth in response to nutrients and TORC2, a complex that regulates cell-cycle dependent polarization of the actin cytoskeleton; involved in meiosis; TOR2 has a paralog, TOR1, that arose from the whole genome duplication","termid":"PBO:0085374"}


id: GO:0150071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of arginase activity.","definition_xrefs":["GOC:bc","GOC:aruk"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of arginase activity (obsolete GO:0150071)","termid":"GO:0150071"}


id: PBO:0030281
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mislocalized_equatorial_microtubule_organizing_center","termid":"PBO:0030281"}


id: PBO:0060694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 2","termid":"PBO:0060694"}


id: PBO:0040421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP6V0D1 divergent transcript","termid":"PBO:0040421"}


id: MONDO:0020189
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete eyebrow/eyelashes structural anomaly (obsolete MONDO:0020189)","secondary_identifiers":["Orphanet:98599"],"termid":"MONDO:0020189","xrefs":{"Monarch":{"xref_id":"0020189"}}}


id: PBO:0061939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 1 subfamily N member 2","termid":"PBO:0061939"}


id: PBO:0058018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3944","termid":"PBO:0058018"}


id: GO:0014062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of serotonin.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of monoatomic ion transport","termid":"GO:0043269"},{"relation_name":"is_a","term_name":"regulation of secretion by cell","termid":"GO:1903530"},{"relation_name":"regulates","term_name":"serotonin secretion","termid":"GO:0001820"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of serotonin secretion","synonyms":[{"name":"regulation of serotonin release","type":"related"}],"termid":"GO:0014062"}


id: PBO:0046354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 12","termid":"PBO:0046354"}


id: GO:0062127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of primary fatty amides.","definition_xrefs":["PMID:11128635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid primary amide metabolic process","termid":"GO:0062126"},{"relation_name":"is_a","term_name":"fatty acid derivative catabolic process","termid":"GO:1901569"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"fatty acid primary amide catabolic process","synonyms":[{"name":"primary fatty amide catabolic process","type":"exact"}],"termid":"GO:0062127"}


id: GO:0004245
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the preferential cleavage at the amino group of hydrophobic residues in insulin, casein, hemoglobin, and a number of other proteins and polypeptides.","definition_xrefs":["GOC:curator"],"gene_count":0,"genotype_count":0,"name":"obsolete neprilysin activity (obsolete GO:0004245)","synonyms":[{"name":"CALLA","type":"related"},{"name":"CALLA (common acute lymphoblastic leukemia-associated) antigens","type":"related"},{"name":"CALLA antigen","type":"related"},{"name":"CALLA glycoprotein","type":"related"},{"name":"CALLA glycoproteins","type":"related"},{"name":"CD10","type":"related"},{"name":"acute lymphoblastic leukemia antigen","type":"related"},{"name":"common acute lymphoblastic leukemia antigen","type":"related"},{"name":"common acute lymphoblastic leukemia-associated antigens","type":"related"},{"name":"endopeptidase 24.11","type":"related"},{"name":"endopeptidase-2 activity","type":"broad"},{"name":"enkephalinase activity","type":"related"},{"name":"kidney-brush-border neutral endopeptidase","type":"narrow"},{"name":"kidney-brush-border neutral peptidase","type":"narrow"},{"name":"kidney-brush-border neutral proteinase activity","type":"narrow"},{"name":"membrane metalloendopeptidase activity","type":"narrow"},{"name":"neprilysin activity","type":"exact"},{"name":"neutral endopeptidase 24.11","type":"related"},{"name":"neutral endopeptidase activity","type":"related"},{"name":"neutral metallendopeptidase activity","type":"related"}],"termid":"GO:0004245"}


id: GO:0072710
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 hydroxyurea stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to hydroxyurea","synonyms":[{"name":"response to HU","type":"exact"}],"termid":"GO:0072710"}


id: PBO:0116601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KANK1 antisense RNA 1","termid":"PBO:0116601"}


id: PBO:0059977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 22","termid":"PBO:0059977"}


id: MONDO:0012136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The neonatal form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the lethal form of the disease which presents with multisystem failure.","definition_xrefs":["Orphanet:228308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carnitine palmitoyltransferase II deficiency","termid":"MONDO:0015515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"carnitine palmitoyl transferase II deficiency, neonatal form","secondary_identifiers":["NANDO:2201132","GARD:17151","UMLS:C1833518","OMIM:608836","MESH:C563463","MEDGEN:318896"],"synonyms":[{"name":"CARNITINE PALMITOYLTRANSFERASE II deficiency, lethal neonatal","type":"related"},{"name":"CPT 2 deficiency, lethal neonatal","type":"related"},{"name":"CPT II deficiency, lethal neonatal","type":"exact"},{"name":"CPT2, lethal systemic form","type":"exact"},{"name":"CPT2, neonatal form","type":"exact"},{"name":"CPTII, lethal systemic form","type":"exact"},{"name":"CPTII, neonatal form","type":"exact"},{"name":"Carnitine Palmitoyltransferase 2 deficiency, antenatal","type":"related"},{"name":"Carnitine Palmitoyltransferase 2 deficiency, lethal neonatal","type":"related"},{"name":"Carnitine Palmitoyltransferase 2 deficiency, neonatal","type":"related"},{"name":"Carnitine palmitoyl transferase II deficiency, lethal systemic form","type":"exact"},{"name":"Carnitine palmitoyl transferase deficiency type 2, lethal systemic form","type":"exact"},{"name":"Carnitine palmitoyl transferase deficiency type 2, neonatal form","type":"exact"},{"name":"Cpt2 deficiency, lethal neonatal","type":"related"},{"name":"carnitine palmitoyl transferase II deficiency, neonatal form","type":"exact"}],"termid":"MONDO:0012136","xrefs":{"Monarch":{"xref_id":"0012136"}}}


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:0010137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOXA2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial thyroid dyshormonogenesis","termid":"MONDO:0010132"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"thyroid dyshormonogenesis 5","secondary_identifiers":["GARD:18192","OMIM:274900","MESH:C562771","UMLS:C0342196","MEDGEN:87430","SCTID:63127008","DOID:0112184"],"synonyms":[{"name":"DUOXA2 familial thyroid dyshormonogenesis","type":"exact"},{"name":"TDH5","type":"exact"},{"name":"familial thyroid dyshormonogenesis caused by mutation in DUOXA2","type":"exact"},{"name":"hypothyroidism, congenital, due to dyshormonogenesis, 5","type":"exact"},{"name":"thyroid dyshormonogenesis 5","type":"exact"},{"name":"thyroid dyshormonogenesis type 5","type":"exact"},{"name":"thyroid hormonogenesis, genetic defect in, 5","type":"exact"}],"termid":"MONDO:0010137","xrefs":{"Monarch":{"xref_id":"0010137"}}}


id: GO:0051055
data:
  {"annotated_genes":["SJAG_02380","SJAG_03940","SJAG_01906","SJAG_00053","SJAG_03170","SJAG_02104","SJAG_03130","SJAG_01187"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90751,104694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[94222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"},{"annotations":[71211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045717"},{"annotations":[115781,111680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"},{"annotations":[113052,110038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071072"}]},"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 lipids.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"negative regulation of lipid metabolic process","termid":"GO:0045833"},{"relation_name":"is_a","term_name":"regulation of lipid biosynthetic process","termid":"GO:0046890"},{"relation_name":"negatively_regulates","term_name":"lipid biosynthetic process","termid":"GO:0008610"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_01187":null,"SJAG_01906":null,"SJAG_02104":null,"SJAG_02380":null,"SJAG_03130":null,"SJAG_03170":null,"SJAG_03940":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of lipid biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of lipid biosynthetic process","type":"exact"},{"name":"down-regulation of lipid biosynthetic process","type":"exact"},{"name":"downregulation of lipid biosynthetic process","type":"exact"},{"name":"inhibition of lipid biosynthetic process","type":"narrow"},{"name":"negative regulation of lipid anabolism","type":"exact"},{"name":"negative regulation of lipid biosynthesis","type":"exact"},{"name":"negative regulation of lipid formation","type":"exact"},{"name":"negative regulation of lipid synthesis","type":"exact"},{"name":"negative regulation of lipogenesis","type":"exact"}],"termid":"GO:0051055","terms_by_termid":{"GO:0010895":null,"GO:0045717":null,"GO:0071072":null,"GO:1902647":null,"GO:2001211":null}}


id: PBO:0027384
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-incomplete_mitotic_sister_chromatid_segregation,_with_chromatin_bridge","termid":"PBO:0027384"}


id: PBO:0065222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 4","termid":"PBO:0065222"}


id: PBO:0117040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AOPEP antisense RNA 1","termid":"PBO:0117040"}


id: PBO:0018062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 Ubc8 (predicted)","termid":"PBO:0018062"}


id: GO:0000741
data:
  {"annotated_genes":["SJAG_01370","SJAG_01613","SJAG_02737","SJAG_02286","SJAG_04936","SJAG_02045","SJAG_00810"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99546,91725,88100,111773,117242,91334,78992],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000742"},{"annotations":[78993],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048288"}]},"cv_name":"biological_process","definition":"The creation of a single nucleus from multiple nuclei as a result of fusing the lipid bilayers that surround each nuclei.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus organization","termid":"GO:0006997"},{"relation_name":"is_a","term_name":"organelle fusion","termid":"GO:0048284"},{"relation_name":"part_of","term_name":"nucleus organization","termid":"GO:0006997"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00810":null,"SJAG_01370":null,"SJAG_01613":null,"SJAG_02045":null,"SJAG_02286":null,"SJAG_02737":null,"SJAG_04936":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"karyogamy","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Karyogamy","GO:0007335"],"synonyms":[{"name":"nuclear fusion","type":"exact"},{"name":"nuclear fusion during karyogamy","type":"exact"}],"termid":"GO:0000741","terms_by_termid":{"GO:0000742":null,"GO:0048288":null}}


id: PBO:0073585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shieldin complex subunit 2 pseudogene 1","termid":"PBO:0073585"}


id: PBO:0027352
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_oxygen_consumption_during_stationary_phase","termid":"PBO:0027352"}


id: SO:0002282
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Terminal inverted repeat (TIR) transposons of the superfamily Transib contain the DDE motif, which is related to the RAG1 protein involved in V(D)J recombination.","definition_xrefs":["PMID:17984973"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transib_TIR_transposon","synonyms":[{"name":"DTR transposon","type":"exact"},{"name":"Transib TIR transposon","type":"exact"},{"name":"transib transposon","type":"exact"}],"termid":"SO:0002282"}


id: PBO:0063750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 15","termid":"PBO:0063750"}


id: PBO:0060861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIMA-related kinase 4 pseudogene 3","termid":"PBO:0060861"}


id: GO:0009337
data:
  {"annotated_genes":["SJAG_01693","SJAG_05027"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70553,117776],"is_not":false,"summary":null,"term":"GO:0009337"}]},"cv_name":"cellular_component","definition":"A multisubunit iron flavoprotein, which in yeast is composed of 2 alpha and 2 beta subunits. Catalyzes the reduction of sulfite to sulfide.","definition_xrefs":["GOC:jl","PMID:6751400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01693":null,"SJAG_05027":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"sulfite reductase complex (NADPH)","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"sulphite reductase complex (NADPH)","type":"exact"}],"termid":"GO:0009337","terms_by_termid":{"GO:0009337":null}}


id: GO:0051519
data:
  {"annotated_genes":["SJAG_03581","SJAG_02392","SJAG_00514"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90204,94914,96180],"is_not":false,"summary":null,"term":"GO:0051519"}]},"cv_name":"biological_process","definition":"Any process that initiates the inactive process of bipolar cell growth, polarized growth from both ends of a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of bipolar cell growth","termid":"GO:0051518"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_02392":null,"SJAG_03581":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"activation of bipolar cell growth","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0051519","terms_by_termid":{"GO:0051519":null}}


id: PBO:0059155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallophosphoesterase 1","termid":"PBO:0059155"}


id: PR:O13647
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC8D2.11 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C8D2.11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC8D2.11","synonyms":[{"name":"Spom972h-SPBC8D2.11","type":"exact"}],"termid":"PR:O13647"}


id: FYPO:0002372
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which all cells in the population are viable and are shaped in the form of spheroids.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete viable spheroid vegetative cell population (obsolete FYPO:0002372)","synonyms":[{"name":"population of spheroid viable cells","type":"exact"},{"name":"viable rounded vegetative cell population","type":"exact"}],"termid":"FYPO:0002372"}


id: PBO:0090145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pex16 family peroxisome import protein Pex16","termid":"PBO:0090145"}


id: PBO:0108777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulator of Heat Sensitivity","termid":"PBO:0108777"}


id: GO:0014885
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events by which an injury stimulus is received and converted into a molecular signal. This occurs as part of the regulation of muscle adaptation.","definition_xrefs":["GOC:mtg_muscle","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of wounding","termid":"GO:0014822"},{"relation_name":"is_a","term_name":"response to injury involved in regulation of muscle adaptation","termid":"GO:0014876"}],"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 injury involved in regulation of muscle adaptation","synonyms":[{"name":"detection of injury involved in regulation of muscle plasticity","type":"related"}],"termid":"GO:0014885"}


id: GO:0044360
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism effects a change in the frequency, rate or extent of the activity of a voltage-gated potassium channel in another organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of voltage-gated potassium channel activity in another organism (obsolete GO:0044360)","synonyms":[{"name":"modulation of voltage-gated potassium channel activity in other organism","type":"exact"}],"termid":"GO:0044360"}


id: PBO:0065259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 23C","termid":"PBO:0065259"}


id: GO:0048834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the number of petals formed in a flower.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of floral organ number","termid":"GO:0048833"},{"relation_name":"part_of","term_name":"corolla development","termid":"GO:0048465"}],"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":"specification of petal number","termid":"GO:0048834"}


id: PATO:0001304
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A variability quality inhering in a bearer by virtue of whether the bearer exhibits temperature variation or change.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"variability","termid":"PATO:0001303"},{"relation_name":"towards","term_name":"temperature","termid":"PATO:0000146"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variability of temperature","termid":"PATO:0001304"}


id: PBO:0053508
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 492","termid":"PBO:0053508"}


id: PR:O60153
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC19C7.04c gene.","definition_xrefs":["UniProtKB:O60153","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C19C7.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C7.04c","synonyms":[{"name":"Spom972h-SPBC19C7.04c","type":"exact"}],"termid":"PR:O60153"}


id: GO:0010271
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of chlorophyll.","definition_xrefs":["PMID:16361392"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chlorophyll metabolic process","termid":"GO:0090056"},{"relation_name":"is_a","term_name":"regulation of tetrapyrrole catabolic process","termid":"GO:1901404"},{"relation_name":"regulates","term_name":"chlorophyll catabolic process","termid":"GO:0015996"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"regulation of chlorophyll catabolic process","termid":"GO:0010271"}


id: MONDO:1010120
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sudden death in children < 19 years of age that remains unexplained after a thorough case investigation, including performance of a complete autopsy with ancillary testing, and review of the clinical history and circumstances of death.","definition_xrefs":["PMID:28679642"],"direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sudden unexpected death in pediatrics","synonyms":[{"name":"SUDP","type":"exact"}],"termid":"MONDO:1010120","xrefs":{"Monarch":{"xref_id":"1010120"}}}


id: PBO:0091634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sub-telomeric 5Tm protein family Ftm3","termid":"PBO:0091634"}


id: MONDO:0030366
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dilated cardiomyopathy that is characterized by neonatal or early childhood onset of dilated cardiomyopathy, with rapid progression to cardiac failure and death unless patients undergo cardiac transplantation and that has material basis in homozygous or compound heterozygous mutation in the JPH2 gene on chromosome 20q13.","definition_xrefs":["DOID:0081161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiomyopathy, dilated, 2E","secondary_identifiers":["MEDGEN:1794180","OMIM:619492","UMLS:C5561970"],"synonyms":[{"name":"CMD2E","type":"exact"},{"name":"cardiomyopathy, dilated, 2E","type":"exact"}],"termid":"MONDO:0030366","xrefs":{"Monarch":{"xref_id":"0030366"}}}


id: GO:0004018
data:
  {"annotated_genes":["SJAG_02850"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77153],"is_not":false,"summary":null,"term":"GO:0004018"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: N6-(1,2-dicarboxyethyl)AMP = fumarate + AMP.","definition_xrefs":["RHEA:16853"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amidine-lyase activity","termid":"GO:0016842"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02850":null},"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":"N6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R01083","MetaCyc:AMPSYN-RXN"],"synonyms":[{"name":"6-N-(1,2-dicarboxyethyl)AMP AMP-lyase activity","type":"related"},{"name":"N6-(1,2-dicarboxyethyl)AMP AMP-lyase activity","type":"related"},{"name":"adenylosuccinase activity","type":"broad"},{"name":"adenylosuccinate lyase activity","type":"broad"},{"name":"succino AMP-lyase activity","type":"broad"}],"termid":"GO:0004018","terms_by_termid":{"GO:0004018":null}}


id: GO:1904967
data:
  {"annotated_genes":["SJAG_01837"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116979],"is_not":false,"summary":null,"term":"GO:1904967"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of attachment of spindle microtubules to kinetochore involved in homologous chromosome segregation.","definition_xrefs":["GOC:vw","PMID:21920317","PMID:23770679","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of attachment of spindle microtubules to kinetochore","termid":"GO:0051988"},{"relation_name":"is_a","term_name":"repair of kinetochore microtubule attachment defect","termid":"GO:0140274"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"part_of","term_name":"meiotic metaphase I homologous chromosome alignment","termid":"GO:0043060"},{"relation_name":"regulates","term_name":"spindle attachment to meiosis I kinetochore","termid":"GO:0051455"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01837":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0140013","GO:0008150"],"is_obsolete":false,"name":"regulation of spindle attachment to meiosis I kinetochore","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0090699"],"synonyms":[{"name":"correction of merotelic kinetochore attachment, meiosis I","type":"related"},{"name":"regulation of attachment of spindle microtubules to kinetochore during meiosis I","type":"related"},{"name":"regulation of attachment of spindle microtubules to kinetochore involved in homologous chromosome segregation","type":"exact"},{"name":"regulation of attachment of spindle microtubules to kinetochore involved in meiosis I","type":"exact"},{"name":"regulation of monopolar attachment","type":"exact"},{"name":"regulation of sister kinetochore mono-orientation","type":"exact"},{"name":"repair of merotelic kinetochore attachment defect, meiosis I","type":"related"}],"termid":"GO:1904967","terms_by_termid":{"GO:1904967":null}}


id: GO:0000991
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to an RNA polymerase II (Pol II) complex, typically composed of twelve subunits, in order to modulate transcription. A protein binding transcription factor may or may not also interact with the template nucleic acid (either DNA or RNA) as well.","definition_xrefs":["GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription factor activity, core RNA polymerase II binding (obsolete GO:0000991)","synonyms":[{"name":"core RNA polymerase II binding transcription factor activity","type":"exact"}],"termid":"GO:0000991"}


id: PBO:0064649
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTPRF interacting protein alpha 1","termid":"PBO:0064649"}


id: PBO:0051628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ilvB acetolactate synthase like","termid":"PBO:0051628"}


id: PBO:0003715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein Pop3","termid":"PBO:0003715"}


id: GO:0072086
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the loop of Henle of the kidney nephron acquires its identity.","definition_xrefs":["GOC:bf","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of nephron tubule identity","termid":"GO:0072081"},{"relation_name":"part_of","term_name":"loop of Henle development","termid":"GO:0072070"}],"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":"specification of loop of Henle identity","secondary_identifiers":["GO:0072083"],"synonyms":[{"name":"specification of intermediate tubule identity","type":"exact"}],"termid":"GO:0072086"}


id: GO:0050978
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive an electrical stimulus relating to a magnetic field, convert it to a molecular signal, and recognize and characterize the signal. Movement in a magnetic field results in an induced electric field, which can be perceived by organisms such as elasmobranch fish.","definition_xrefs":["PMID:15886990","Wikipedia:Magnetoception","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory perception of electrical stimulus","termid":"GO:0050952"},{"relation_name":"is_a","term_name":"magnetoreception","termid":"GO:0050958"}],"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":"magnetoreception by sensory perception of electrical stimulus","synonyms":[{"name":"magnetoreception by electrical stimulus","type":"exact"},{"name":"magnetoreception through electrical stimulus","type":"exact"},{"name":"magnetoreception, sensory perception of electrical stimulus","type":"exact"},{"name":"magnetoreception, using electrical stimulus","type":"exact"}],"termid":"GO:0050978"}


id: MONDO:1010278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent Mullerian duct syndrome that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"difference of sexual differentiation, non-human animal","termid":"MONDO:0700105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent Mullerian duct syndrome, non-human animal","secondary_identifiers":["OMIA:000791"],"termid":"MONDO:1010278","xrefs":{"Monarch":{"xref_id":"1010278"}}}


id: GO:1902516
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to sn-glycerol 3-phosphate.","definition_xrefs":["PMID:23013274","GOC:TermGenie","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"carbohydrate derivative binding","termid":"GO:0097367"}],"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":"sn-glycerol 3-phosphate binding","termid":"GO:1902516"}


id: PBO:0080806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-ray repair cross complementing 2","termid":"PBO:0080806"}


id: MONDO:0010582
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete diabetes insipidus, neurohypophyseal type, X-linked inheritance (obsolete MONDO:0010582)","secondary_identifiers":["OMIM:304900","DOID:0081059"],"synonyms":[{"name":"diabetes insipidus, neurohypophyseal type","type":"exact"}],"termid":"MONDO:0010582","xrefs":{"Monarch":{"xref_id":"0010582"}}}


id: PBO:0045894
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 gamma pseudogene 6","termid":"PBO:0045894"}


id: PBO:0042471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell division cycle associated 8","termid":"PBO:0042471"}


id: PBO:0090035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclophilin family peptidyl-prolyl cis-trans isomerase Cyp3","termid":"PBO:0090035"}


id: PBO:0045698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein light chain Tctex-type 3 pseudogene 2","termid":"PBO:0045698"}


id: MONDO:0021075
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"polyp","termid":"MONDO:0005079"},{"relation_name":"is_a","term_name":"precancerous condition","termid":"MONDO:0021074"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplastic polyp","secondary_identifiers":["NCIT:C7068","MEDGEN:233751","UMLS:C1334941"],"synonyms":[{"name":"neoplastic polyp","type":"exact"}],"termid":"MONDO:0021075","xrefs":{"Monarch":{"xref_id":"0021075"}}}


id: GO:0015820
data:
  {"annotated_genes":["SJAG_00991","SJAG_03591","SJAG_03970","SJAG_05346"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88431],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905533"},{"annotations":[93676,92082,99205],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905534"}]},"cv_name":"biological_process","definition":"The directed movement of L-leucine, 2-amino-4-methylpentanoic 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:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"branched-chain amino acid transport","termid":"GO:0015803"},{"relation_name":"is_a","term_name":"neutral amino acid transport","termid":"GO:0015804"},{"relation_name":"is_a","term_name":"L-amino acid transport","termid":"GO:0015807"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00991":null,"SJAG_03591":null,"SJAG_03970":null,"SJAG_05346":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"L-leucine transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"leucine transport","type":"broad"}],"termid":"GO:0015820","terms_by_termid":{"GO:1905533":null,"GO:1905534":null}}


id: GO:1903159
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any malate transmembrane transporter activity that is involved in malate import into cell.","definition_xrefs":["GO_REF:0000061","GOC:TermGenie","ISBN:0-8249-3695-6","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete malate transmembrane transporter activity involved in malate import into cell (obsolete GO:1903159)","synonyms":[{"name":"dicarboxylate (succinate/fumarate/malate) antiporter activity involved in malate import into cell","type":"related"},{"name":"malate transmembrane transporter activity involved in malate import into cell","type":"exact"}],"termid":"GO:1903159"}


id: PBO:0030066
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_phosphoglycerate_mutase_activity","termid":"PBO:0030066"}


id: GO:0001814
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of antibody-dependent cellular cytotoxicity.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of type IIa hypersensitivity","termid":"GO:0001797"},{"relation_name":"is_a","term_name":"regulation of antibody-dependent cellular cytotoxicity","termid":"GO:0001813"},{"relation_name":"is_a","term_name":"negative regulation of leukocyte mediated cytotoxicity","termid":"GO:0001911"},{"relation_name":"negatively_regulates","term_name":"antibody-dependent cellular cytotoxicity","termid":"GO:0001788"}],"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 antibody-dependent cellular cytotoxicity","synonyms":[{"name":"down regulation of antibody-dependent cellular cytotoxicity","type":"exact"},{"name":"down-regulation of antibody-dependent cellular cytotoxicity","type":"exact"},{"name":"downregulation of antibody-dependent cellular cytotoxicity","type":"exact"},{"name":"inhibition of antibody-dependent cellular cytotoxicity","type":"narrow"},{"name":"negative regulation of antibody dependent cell death","type":"exact"},{"name":"negative regulation of antibody dependent cell killing","type":"exact"},{"name":"negative regulation of antibody-dependent cell death","type":"exact"},{"name":"negative regulation of antibody-dependent cell killing","type":"exact"}],"termid":"GO:0001814"}


id: PBO:0034585
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-slow_vegetative_cell_population_growth_followed_by_return_to_normal_growth_rate","termid":"PBO:0034585"}


id: PBO:0059896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND1 pseudogene 19","termid":"PBO:0059896"}


id: GO:1904668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ubiquitin protein ligase activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","GOC:vw","GOC:dph","PMID:10921876","PMID:26216882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of ubiquitin-protein transferase activity","termid":"GO:0051443"},{"relation_name":"is_a","term_name":"regulation of ubiquitin protein ligase activity","termid":"GO:1904666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"positively_regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"positive regulation of ubiquitin protein ligase activity","secondary_identifiers":["GO:0051488","GO:0090623","GO:1903835","GO:0007092"],"synonyms":[{"name":"activation of APC-Cdc20 complex activity","type":"narrow"},{"name":"activation of APC-fizzy related complex activity","type":"narrow"},{"name":"activation of E3","type":"related"},{"name":"activation of anaphase-promoting complex activity","type":"narrow"},{"name":"activation of protein ubiquitination activity","type":"narrow"},{"name":"activation of ubiquitin ligase activity","type":"narrow"},{"name":"activation of ubiquitin protein ligase activity","type":"narrow"},{"name":"positive regulation of APC-fizzy related complex activity","type":"narrow"},{"name":"positive regulation of E3","type":"related"},{"name":"positive regulation of protein ubiquitination activity","type":"exact"},{"name":"positive regulation of ubiquitin ligase activity","type":"related"},{"name":"up regulation of APC-fizzy related complex activity","type":"narrow"},{"name":"up regulation of E3","type":"related"},{"name":"up regulation of protein ubiquitination activity","type":"exact"},{"name":"up regulation of ubiquitin ligase activity","type":"exact"},{"name":"up regulation of ubiquitin protein ligase activity","type":"exact"},{"name":"up-regulation of APC-fizzy related complex activity","type":"narrow"},{"name":"up-regulation of E3","type":"related"},{"name":"up-regulation of protein ubiquitination activity","type":"exact"},{"name":"up-regulation of ubiquitin ligase activity","type":"exact"},{"name":"up-regulation of ubiquitin protein ligase activity","type":"exact"},{"name":"upregulation of APC-fizzy related complex activity","type":"narrow"},{"name":"upregulation of E3","type":"related"},{"name":"upregulation of protein ubiquitination activity","type":"exact"},{"name":"upregulation of ubiquitin ligase activity","type":"exact"},{"name":"upregulation of ubiquitin protein ligase activity","type":"exact"}],"termid":"GO:1904668"}


id: PBO:0074253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLCO1B3-SLCO1B7 readthrough","termid":"PBO:0074253"}


id: PBO:0050014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class I, B","termid":"PBO:0050014"}


id: SO:0001361
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Five_methoxycarbonylmethyl_2_prime_O_methyluridine is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_methoxycarbonylmethyl_two_prime_O_methyluridine","secondary_identifiers":["RNAMOD:069"],"synonyms":[{"name":"5-methoxycarbonylmethyl-2'-O-methyluridine","type":"exact"},{"name":"five methoxycarbonylmethyl two prime O methyluridine","type":"exact"},{"name":"mcm5Um","type":"exact"}],"termid":"SO:0001361"}


id: GO:0032126
data:
  {"annotated_genes":["SJAG_02989","SJAG_02626","SJAG_02087","SJAG_04227","SJAG_02338","SJAG_02707"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[99302,104188,118142],"is_not":false,"summary":null,"term":"GO:0032126"},{"annotations":[70150,92239,71724],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036286"}]},"cv_name":"cellular_component","definition":"A cell part that is composed of the eisosome membrane or MCC domain, a furrow-like plasma membrane sub-domain and associated integral transmembrane proteins, and the proteins (eisosome filaments) that form a scaffolding lattice on the cytoplasmic face. Eisosomes broadly affect overall plasma membrane organization.","definition_xrefs":["GOC:vw","PMID:16496001","GOC:al","PMID:22368779"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02087":null,"SJAG_02338":null,"SJAG_02626":null,"SJAG_02707":null,"SJAG_02989":null,"SJAG_04227":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"eisosome","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Eisosome"],"termid":"GO:0032126","terms_by_termid":{"GO:0032126":null,"GO:0036286":null}}


id: PBO:0082954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic proteinase A (Pep4p) inhibitor; dependent on Pbs2p and Hog1p protein kinases for osmotic induction; intrinsically unstructured, N-terminal half becomes ordered in the active site of proteinase A upon contact","termid":"PBO:0082954"}


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


id: MONDO:0000519
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A oligodendroglioma that involves the corpus callosum.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain oligodendroglioma","termid":"MONDO:0002544"},{"relation_name":"is_a","term_name":"cerebral hemisphere cancer","termid":"MONDO:0002731"}],"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":"corpus callosum oligodendroglioma","secondary_identifiers":["DOID:0050901"],"synonyms":[{"name":"corpus callosum oligodendroglioma","type":"exact"},{"name":"oligodendroglioma of corpus callosum","type":"exact"}],"termid":"MONDO:0000519","xrefs":{"Monarch":{"xref_id":"0000519"}}}


id: SO:0001803
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript processing variant whereby polyadenylation of the encoded transcript is decreased with respect to the reference.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyadenylation_variant","termid":"SO:0001545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased_polyadenylation_variant","synonyms":[{"name":"decreased polyadenylation variant","type":"exact"}],"termid":"SO:0001803"}


id: FYPO:0008124
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A abnormal nuclear envelope organization phenotype in which SPB fenestra in the nuclear envelope are larger than normal. SPB fenestra are the result of SPB extrusion.","definition_xrefs":["PMID:37783794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear envelope organization","termid":"FYPO:0000815"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased nuclear envelope SPB fenestra size","termid":"FYPO:0008124"}


id: MONDO:0019257
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemochromatosis type 2 (juvenile) is the early-onset and most severe form of rare hereditary hemochromatosis (HH), a group of diseases characterized by excessive tissue iron deposition of genetic origin.","definition_xrefs":["Orphanet:79230"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemochromatosis","termid":"MONDO:0006507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hemochromatosis type 2","secondary_identifiers":["SCTID:50855007","NORD:1315","GARD:10092","DOID:0111034","UMLS:C0268060","MEDGEN:82769","MESH:C537247"],"synonyms":[{"name":"HFE2","type":"exact"},{"name":"JHH","type":"exact"},{"name":"Juvenile Hemochromatosis","type":"exact"},{"name":"hemochromatosis juvenile","type":"related"},{"name":"iron overload disease juvenile","type":"related"},{"name":"juvenile hemochromatosis","type":"exact"}],"termid":"MONDO:0019257","xrefs":{"Monarch":{"xref_id":"0019257"}}}


id: PBO:0117115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SFSWAP antisense RNA 1","termid":"PBO:0117115"}


id: PBO:0050347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 50","termid":"PBO:0050347"}


id: GO:0051669
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of terminal, non-reducing 2,1- and 2,6-linked beta-D-fructofuranose residues in fructans.","definition_xrefs":["EC:3.2.1.80"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016798","GO:0003824"],"is_obsolete":false,"name":"fructan beta-fructosidase activity","secondary_identifiers":["MetaCyc:3.2.1.80-RXN"],"synonyms":[{"name":"beta-D-fructan fructohydrolase activity","type":"related"},{"name":"exo-beta-D-fructosidase activity","type":"exact"},{"name":"exo-beta-fructosidase activity","type":"exact"},{"name":"fructan b-fructosidase activity","type":"exact"},{"name":"fructan exohydrolase activity","type":"exact"},{"name":"fructanase activity","type":"related"},{"name":"polysaccharide beta-fructofuranosidase activity","type":"exact"}],"termid":"GO:0051669"}


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":["ICD9:032.0","MEDGEN:3857","SCTID:3419005","UMLS:C0012556"],"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: PBO:0088052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-like protein involved in thiolation of cytoplasmic tRNAs; receives sulfur from the E1-like enzyme Uba4p and transfers it to tRNA; also functions as a protein tag with roles in nutrient sensing and oxidative stress response","termid":"PBO:0088052"}


id: MONDO:1012937
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurodegenerative disease characterized by severe ataxia, rigidity, and tremor with neuronal loss, spongiosis, and widespread Lewy body-like inclusions in many regions of the brain including the midbrain, basal ganglia, and neocortex that occurs in yellow-crowned parrot due to a mutation in the CADPS2 gene.","definition_xrefs":["PMID:36086934"],"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":"neurodegenerative disease, non-human animal","termid":"MONDO:1012953"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lewy body-like disease, CADPS2-related, yellow-crowned parrot","secondary_identifiers":["OMIA:002573-151761"],"termid":"MONDO:1012937","xrefs":{"Monarch":{"xref_id":"1012937"}}}


id: PBO:0090326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lgl family protein Sro7","termid":"PBO:0090326"}


id: GO:1903750
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of intrinsic apoptotic signaling pathway in response to hydrogen peroxide.","definition_xrefs":["GO_REF:0000058","PMID:18681888","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hydrogen peroxide-mediated programmed cell death","termid":"GO:1901298"},{"relation_name":"is_a","term_name":"regulation of oxidative stress-induced intrinsic apoptotic signaling pathway","termid":"GO:1902175"},{"relation_name":"regulates","term_name":"intrinsic apoptotic signaling pathway in response to hydrogen peroxide","termid":"GO:0036481"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","synonyms":[{"name":"regulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"regulation of hydrogen peroxide-induced apoptosis","type":"broad"},{"name":"regulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"regulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"}],"termid":"GO:1903750"}


id: PR:O74872
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug111 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 111 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC31H12.06","synonyms":[{"name":"Spom972h-mug111","type":"exact"}],"termid":"PR:O74872"}


id: PBO:0003001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nitric oxide dioxygenase (predicted)","termid":"PBO:0003001"}


id: RO:0002089
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"temporally_related_to","termid":"RO:0002222"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"starts_before","termid":"RO:0002089"}


id: GO:0045967
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces the rate of growth of all or part of an organism.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of growth rate","termid":"GO:0040009"},{"relation_name":"is_a","term_name":"negative regulation of growth","termid":"GO:0045926"}],"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 growth rate","synonyms":[{"name":"down regulation of growth rate","type":"exact"},{"name":"down-regulation of growth rate","type":"exact"},{"name":"downregulation of growth rate","type":"exact"},{"name":"inhibition of growth rate","type":"narrow"}],"termid":"GO:0045967"}


id: GO:0043377
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of CD8-positive, alpha-beta T cell differentiation.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of CD8-positive, alpha-beta T cell differentiation","termid":"GO:0043376"},{"relation_name":"is_a","term_name":"negative regulation of alpha-beta T cell differentiation","termid":"GO:0046639"},{"relation_name":"is_a","term_name":"negative regulation of CD8-positive, alpha-beta T cell activation","termid":"GO:2001186"},{"relation_name":"negatively_regulates","term_name":"CD8-positive, alpha-beta T cell differentiation","termid":"GO:0043374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of CD8-positive, alpha-beta T cell differentiation","synonyms":[{"name":"down regulation of CD8-positive, alpha-beta T cell differentiation","type":"exact"},{"name":"down-regulation of CD8-positive, alpha-beta T cell differentiation","type":"exact"},{"name":"downregulation of CD8-positive, alpha-beta T cell differentiation","type":"exact"},{"name":"inhibition of CD8-positive, alpha-beta T cell differentiation","type":"narrow"},{"name":"negative regulation of CD8-positive T lymphocyte differentiation","type":"exact"},{"name":"negative regulation of CD8-positive T-cell differentiation","type":"exact"},{"name":"negative regulation of CD8-positive T-lymphocyte differentiation","type":"exact"},{"name":"negative regulation of CD8-positive, alpha beta T lymphocyte differentiation","type":"exact"},{"name":"negative regulation of CD8-positive, alpha beta T-cell differentiation","type":"exact"},{"name":"negative regulation of CD8-positive, alpha beta T-lymphocyte differentiation","type":"exact"},{"name":"negative regulation of CD8-positive, alpha-beta T cell development","type":"related"}],"termid":"GO:0043377"}


id: PBO:0044700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 3 pseudogene 3","termid":"PBO:0044700"}


id: PBO:0044126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTAGE family member 12, pseudogene","termid":"PBO:0044126"}


id: FYPO:0006547
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A localization phenotype observed in the vegetative growth phase of the life cycle in which the distribution of phosphatidylserine (PS) in the plasma membrane is abnormal such that the PS level is lower than normal at one or both cell tips. Normally, PS shows a polarized distribution with a higher concentration at the cell tips than in the lateral plasma membrane.","definition_xrefs":["PMID:27852900","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal plasma membrane phosphatidylserine distribution","termid":"FYPO:0006497"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"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:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"abnormal plasma membrane phosphatidylserine distribution resulting in decreased concentration at cell tip","synonyms":[{"name":"abnormal plasma membrane PS distribution resulting in decreased concentration at cell tip","type":"exact"},{"name":"abnormal plasma membrane phosphatidylserine distribution resulting in decreased concentration at cell tip during mitotic cell cycle","type":"related"},{"name":"abnormal plasma membrane phosphatidylserine distribution resulting in decreased concentration at cell tip during vegetative growth","type":"exact"},{"name":"abnormal plasma membrane phosphatidylserine distribution resulting in reduced concentration at cell tip","type":"exact"},{"name":"decreased plasma membrane phosphatidylserine polarity","type":"related"},{"name":"reduced plasma membrane phosphatidylserine polarity","type":"related"}],"termid":"FYPO:0006547"}


id: PBO:0049032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 19","termid":"PBO:0049032"}


id: PBO:0015661
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae AOS1","termid":"PBO:0015661"}


id: PBO:0001384
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stress response pathway signalling (SRP), mediated phosphorylation of Ser402 regulates the timing of commitment to mitosis","termid":"PBO:0001384"}


id: PBO:0043499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contactin 6","termid":"PBO:0043499"}


id: PBO:0054462
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 1859","termid":"PBO:0054462"}


id: MOD:00973
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Oxidation of proline (to glutamic acid)","termid":"MOD:00973"}


id: MOD:01573
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-119 reporter+balance group.","definition_xrefs":["Unimod:731#Y"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"},{"relation_name":"is_a","term_name":"iTRAQ8plex-119 reporter+balance reagent acylated residue","termid":"MOD:01570"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent O-acylated residue","termid":"MOD:01714"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-119 reporter+balance reagent O4'-acylated tyrosine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Accurate mass for 115, 118, 119 & 121","type":"related"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"iTRAQ8plex:13C(6)15N(2)","type":"related"}],"termid":"MOD:01573"}


id: PBO:0041005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BLOC-1 related complex subunit 7","termid":"PBO:0041005"}


id: PBO:0004376
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.39","termid":"PBO:0004376"}


id: GO:1904021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of G protein-coupled receptor internalization.","definition_xrefs":["GO_REF:0000058","PMID:24732013","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of receptor internalization","termid":"GO:0002091"},{"relation_name":"is_a","term_name":"regulation of G protein-coupled receptor internalization","termid":"GO:1904020"},{"relation_name":"negatively_regulates","term_name":"G protein-coupled receptor internalization","termid":"GO:0002031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052","GO:0016192"],"is_obsolete":false,"name":"negative regulation of G protein-coupled receptor internalization","synonyms":[{"name":"down regulation of G-protein coupled receptor internalization","type":"exact"},{"name":"down-regulation of G-protein coupled receptor internalization","type":"exact"},{"name":"downregulation of G-protein coupled receptor internalization","type":"exact"},{"name":"inhibition of G-protein coupled receptor internalization","type":"narrow"},{"name":"negative regulation of G-protein coupled receptor internalization","type":"exact"}],"termid":"GO:1904021"}


id: MONDO:0008250
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated congenital growth hormone deficiency","termid":"MONDO:0000050"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"isolated growth hormone deficiency type II","secondary_identifiers":["DOID:0060872","MEDGEN:124405","Orphanet:231679","MESH:C562704","GARD:1696","OMIM:173100","SCTID:237687003","UMLS:C0271567"],"synonyms":[{"name":"Growth hormone deficiency, isolated autosomal dominant","type":"related"},{"name":"Growth hormone deficiency, isolated, autosomal dominant","type":"related"},{"name":"IGHD 2","type":"related"},{"name":"IGHD II","type":"exact"},{"name":"IGHD2","type":"related"},{"name":"autosomal dominant isolated growth hormone deficiency","type":"exact"},{"name":"autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency","type":"exact"},{"name":"congenital IGHD type II","type":"exact"},{"name":"congenital isolated GH deficiency type II","type":"exact"},{"name":"congenital isolated growth hormone deficiency type II","type":"exact"},{"name":"growth hormone deficiency, isolated, type II","type":"exact"},{"name":"isolated Growth hormone deficiency, type 2","type":"related"},{"name":"isolated growth hormone deficiency type 2","type":"related"},{"name":"isolated growth hormone deficiency, type II","type":"related"},{"name":"pituitary dwarfism due to isolated Growth hormone deficiency, autosomal dominant","type":"related"},{"name":"pituitary dwarfism due to isolated growth hormone deficiency autosomal dominant","type":"related"}],"termid":"MONDO:0008250","xrefs":{"Monarch":{"xref_id":"0008250"}}}


id: GO:0002413
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process of tolerance induction which leads to immunological tolerance of a tumor.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune response to tumor cell","termid":"GO:0002418"},{"relation_name":"is_a","term_name":"peripheral tolerance induction","termid":"GO:0002465"}],"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":"tolerance induction to tumor cell","termid":"GO:0002413"}


id: PBO:0031062
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,_with_elongated,_septated_germ_tube","termid":"PBO:0031062"}


id: PBO:0054236
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 1618","termid":"PBO:0054236"}


id: PBO:0088815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ragulator complex subunit, human LAMTOR4 ortholog","termid":"PBO:0088815"}


id: PBO:0007962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphotyrosyl phosphatase activator Ypa2","termid":"PBO:0007962"}


id: PBO:0029830
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_curved_stubby_vegetative_cell_population_(obsolete_FYPO:0002407)","termid":"PBO:0029830"}


id: FYPO:0000650
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which the septation index is higher than normal. The septation index is the proportion of the population undergoing septation at any given time, and is usually around 10% (varying between 7-15%) for wild type.","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"increased septation index","synonyms":[{"name":"increased number of septated cells","type":"exact"},{"name":"increased septation","type":"related"},{"name":"septated","type":"related"}],"termid":"FYPO:0000650"}


id: GO:0052621
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 GTP = cyclic di-3',5'-guanylate + 2 diphosphate + 2 H+.","definition_xrefs":["EC:2.7.7.65","RHEA:24898"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotidyltransferase activity","termid":"GO:0016779"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016779","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"diguanylate cyclase activity","secondary_identifiers":["KEGG_REACTION:R08057","MetaCyc:RXN0-5359","GO:0043789"],"synonyms":[{"name":"GTP:GTP guanylyltransferase activity","type":"broad"}],"termid":"GO:0052621"}


id: RO:0002452
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relation that holds between a disease or an organism and a phenotype","direct_ancestors":[{"relation_name":"is_a","term_name":"has_phenotype","termid":"RO:0002200"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_symptom","termid":"RO:0002452"}


id: PBO:0077881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin polymerization promoting protein","termid":"PBO:0077881"}


id: GO:0062062
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an oligosaccharyltransferase complex.","definition_xrefs":["PMID:12887896"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"oligosaccharyltransferase complex binding","termid":"GO:0062062"}


id: CHEBI:2639
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":"amiloride","termid":"CHEBI:2639"}


id: MONDO:0024573
data:
  {"annotated_genes":["SJAG_00547","SJAG_01665","SJAG_02431","SJAG_02536","SJAG_02785","SJAG_03703","SJAG_03126","SJAG_03453","SJAG_01181","SJAG_00228","SJAG_02923","SJAG_03077","SJAG_03145","SJAG_00993","SJAG_02342"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86175],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000015"},{"annotations":[85379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014112"},{"annotations":[85380,85382,85381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014113"},{"annotations":[85385,85386,85387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014114"},{"annotations":[86049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012557"},{"annotations":[85543],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009026"},{"annotations":[85521,85522],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008647"},{"annotations":[86801],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012112"},{"annotations":[86563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012799"},{"annotations":[86811,86810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013197"},{"annotations":[85695],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010946"},{"annotations":[86806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012111"},{"annotations":[87610,87609,87611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008104"},{"annotations":[86129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033669"},{"annotations":[86999],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012371"},{"annotations":[86796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013186"},{"annotations":[85866,85867],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054588"}]},"cv_name":"mondo","definition":"Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.","definition_xrefs":["NCIT:C84773"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrophic cardiomyopathy","termid":"MONDO:0005045"},{"relation_name":"is_a","term_name":"familial cardiomyopathy","termid":"MONDO:0005217"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00228":null,"SJAG_00547":null,"SJAG_00993":null,"SJAG_01181":null,"SJAG_01665":null,"SJAG_02342":null,"SJAG_02431":null,"SJAG_02536":null,"SJAG_02785":null,"SJAG_02923":null,"SJAG_03077":null,"SJAG_03126":null,"SJAG_03145":null,"SJAG_03453":null,"SJAG_03703":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"familial hypertrophic cardiomyopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D024741","DOID:0080326","OMIMPS:192600","Orphanet:155","SCTID:471885006","UMLS:C0949658","MEDGEN:183649"],"synonyms":[{"name":"cardiomyopathy, familial hypertrophic","type":"exact"},{"name":"familial hypertrophic cardiomyopathy","type":"exact"},{"name":"familila or idiopathic hypertrophic obstructive cardiomyopathy","type":"exact"},{"name":"hereditary hypertrophic cardiomyopathy","type":"exact"},{"name":"hypertrophic familial cardiomyopathy","type":"exact"}],"termid":"MONDO:0024573","terms_by_termid":{"MONDO:0008104":null,"MONDO:0008647":null,"MONDO:0009026":null,"MONDO:0010946":null,"MONDO:0012111":null,"MONDO:0012112":null,"MONDO:0012371":null,"MONDO:0012557":null,"MONDO:0012799":null,"MONDO:0013186":null,"MONDO:0013197":null,"MONDO:0014112":null,"MONDO:0014113":null,"MONDO:0014114":null,"MONDO:0033669":null,"MONDO:0054588":null,"MONDO:8000015":null},"xrefs":{"Monarch":{"xref_id":"0024573"}}}


id: MONDO:0012893
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteoarthritis in which the cause of the disease is a mutation in the GDF5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoarthritis susceptibility 5","secondary_identifiers":["SCTID:239872002","OMIM:612400","MEDGEN:1674605","UMLS:C4759728"],"synonyms":[{"name":"GDF5 osteoarthritis","type":"exact"},{"name":"OS5","type":"related"},{"name":"osteoarthritis caused by mutation in GDF5","type":"exact"},{"name":"osteoarthritis of hip","type":"related"},{"name":"osteoarthritis susceptibility 5","type":"exact"},{"name":"osteoarthritis susceptibility type 5","type":"exact"},{"name":"osteoarthritis-5","type":"exact"}],"termid":"MONDO:0012893","xrefs":{"Monarch":{"xref_id":"0012893"}}}


id: GO:0006287
data:
  {"annotated_genes":["SJAG_02818","SJAG_02908"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74536,75381],"is_not":false,"summary":null,"term":"GO:0006287"}]},"cv_name":"biological_process","definition":"Repair of the damaged strand by the combined action of an apurinic endouclease that degrades a few bases on the damaged strand and a polymerase that synthesizes a 'patch' in the 5' to 3' direction, using the undamaged strand as a template.","definition_xrefs":["ISBN:1550091131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolic process","termid":"GO:0006259"},{"relation_name":"part_of","term_name":"base-excision repair","termid":"GO:0006284"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02818":null,"SJAG_02908":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0006281"],"is_obsolete":false,"name":"base-excision repair, gap-filling","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-73933"],"termid":"GO:0006287","terms_by_termid":{"GO:0006287":null}}


id: PBO:0026937
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_localization_to_chromosome","termid":"PBO:0026937"}


id: GO:0042778
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the 3'-terminal CCA of a tRNA is removed and restored. This often happens to uncharged tRNA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA metabolic process","termid":"GO:0006399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0008150","GO:0006399"],"is_obsolete":false,"name":"tRNA end turnover","termid":"GO:0042778"}


id: PBO:0028243
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_glycosylated_protein_in_cell","termid":"PBO:0028243"}


id: GO:0032076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or reduces the rate of deoxyribonuclease activity, the hydrolysis of ester linkages within deoxyribonucleic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nuclease activity","termid":"GO:0032074"},{"relation_name":"is_a","term_name":"negative regulation of DNA metabolic process","termid":"GO:0051053"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"negative regulation of deoxyribonuclease activity","synonyms":[{"name":"DNase inhibitor","type":"related"},{"name":"deoxyribonuclease inhibitor","type":"related"},{"name":"down regulation of deoxyribonuclease activity","type":"exact"},{"name":"down-regulation of deoxyribonuclease activity","type":"exact"},{"name":"downregulation of deoxyribonuclease activity","type":"exact"},{"name":"inhibition of deoxyribonuclease activity","type":"narrow"}],"termid":"GO:0032076"}


id: PBO:0052070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine acetyltransferase 14","termid":"PBO:0052070"}


id: PBO:0047659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 10","termid":"PBO:0047659"}


id: PBO:0061124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family pyrin domain containing 13","termid":"PBO:0061124"}


id: PBO:0030006
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_middle_meiotic_gene_mRNA_during_late_meiosis","termid":"PBO:0030006"}


id: GO:0140569
data:
  {"annotated_genes":["SJAG_01435"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101335],"is_not":false,"summary":null,"term":"GO:0140569"}]},"cv_name":"biological_process","definition":"The removal of a mislocalized protein from the endoplasmic reticulum (ER) membrane.","definition_xrefs":["PMID:32973005"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extraction of mislocalized protein from membrane","termid":"GO:0140568"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01435":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"extraction of mislocalized protein from ER membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140569","terms_by_termid":{"GO:0140569":null}}


id: PR:Q09681
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gmh2 gene.","definition_xrefs":["UniProtKB:Q09681","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":"alpha-1,2-galactosyltransferase gmh2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5H10.13c","synonyms":[{"name":"Spom972h-gmh2","type":"exact"}],"termid":"PR:Q09681"}


id: GO:0010366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of an ethylene biosynthetic process.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ethylene biosynthetic process","termid":"GO:0010364"},{"relation_name":"is_a","term_name":"negative regulation of sulfur amino acid metabolic process","termid":"GO:0031336"},{"relation_name":"is_a","term_name":"negative regulation of olefin biosynthetic process","termid":"GO:1900912"},{"relation_name":"negatively_regulates","term_name":"ethylene biosynthetic process","termid":"GO:0009693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"negatively_regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006790","GO:0008150"],"is_obsolete":false,"name":"negative regulation of ethylene biosynthetic process","termid":"GO:0010366"}


id: GO:1901363
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