# terms

id: PBO:0080214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"villin like","termid":"PBO:0080214"}


id: MONDO:0016359
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Limited systemic sclerosis (lSSc) (or SSc sine scleroderma) is a subset of systemic sclerosis (SSc) characterized by organ involvement in the absence of fibrosis of the skin.","definition_xrefs":["Orphanet:220407"],"direct_ancestors":[{"relation_name":"is_a","term_name":"systemic sclerosis","termid":"MONDO:0005100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"limited systemic sclerosis","secondary_identifiers":["GARD:9749","icd11.foundation:187455179","NCIT:C116789","MEDGEN:220934","SCTID:128461001","UMLS:C1290138"],"synonyms":[{"name":"SSC without skin involvement","type":"exact"},{"name":"Scleroderma, sine","type":"related"},{"name":"progressive systemic sclerosis sine scleroderma","type":"related"},{"name":"systemic sclerosis sine scleroderma","type":"exact"},{"name":"systemic sclerosis without skin involvement","type":"exact"}],"termid":"MONDO:0016359","xrefs":{"Monarch":{"xref_id":"0016359"}}}


id: FYPO:0005385
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the first meiotic nuclear division (part of the meiotic cell cycle) is arrested in metaphase under conditions where arrest does not normally occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"abolished mitotic sister chromatid separation","termid":"FYPO:0001946"},{"relation_name":"is_a","term_name":"abnormally arrested meiosis I","termid":"FYPO:0002817"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abnormal cell cycle arrest in meiotic metaphase I","secondary_identifiers":["FYPO:0006769"],"synonyms":[{"name":"abnormal cell cycle arrest in metaphase I","type":"exact"},{"name":"abnormal cell cycle arrest in metaphase I during meiotic cell cycle","type":"exact"},{"name":"abnormal cell cycle arrest in metaphase during first meiotic nuclear division","type":"exact"},{"name":"abnormal cell cycle arrest in metaphase of meiosis I","type":"exact"},{"name":"abnormal meiotic cell cycle arrest in metaphase I","type":"exact"},{"name":"abolished meiosis I metaphase/anaphase transition","type":"related"}],"termid":"FYPO:0005385"}


id: MOD:00737
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with an N-acetylneuraminic acid (sialic acid) group through a glycosidic bond.","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosylated residue","termid":"MOD:00693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"N-acetylneuraminylated","synonyms":[{"name":"N-acetylneuraminic acid (Sialic acid, NeuAc, NANA, SA)","type":"exact"},{"name":"NeuNAc","type":"exact"}],"termid":"MOD:00737"}


id: GO:1905392
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process by which a plant organ is generated and organized.","definition_xrefs":["GO_REF:0000083","GOC:tb","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"plant organ development","termid":"GO:0099402"}],"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":"plant organ morphogenesis","termid":"GO:1905392"}


id: PBO:0076247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUV39H2 histone lysine methyltransferase","termid":"PBO:0076247"}


id: PBO:0052498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 10","termid":"PBO:0052498"}


id: PBO:0003688
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.7.4","termid":"PBO:0003688"}


id: GO:1902712
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of G protein-coupled GABA receptor activity. In human, it is usually a heterodimer composed of GABA-B receptor subunits 1 and 2.","definition_xrefs":["GOC:bhm","GO_REF:0000088","GOC:TermGenie","PMID:18790874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor dimeric complex","termid":"GO:0038037"},{"relation_name":"is_a","term_name":"GABA receptor complex","termid":"GO:1902710"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"G protein-coupled GABA receptor complex","synonyms":[{"name":"G-protein coupled GABA receptor complex","type":"exact"}],"termid":"GO:1902712"}


id: GO:0009886
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring after animal embryonic development, by which anatomical structures are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"post-embryonic development","termid":"GO:0009791"}],"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":"post-embryonic animal morphogenesis","synonyms":[{"name":"post-embryonic morphogenesis of an anatomical structure","type":"exact"}],"termid":"GO:0009886"}


id: MONDO:0014563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"mitochondrial disease","termid":"MONDO:0044970"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency","secondary_identifiers":["Orphanet:653880","UMLS:C4225391","GARD:13019","MEDGEN:902729","DOID:0070540","OMIM:616277"],"synonyms":[{"name":"ECHS1D","type":"related"},{"name":"mitochondrial short-chain ENOYL-CoA hydratase 1 deficiency","type":"related"},{"name":"mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency","type":"exact"},{"name":"short-chain enoyl-CoA hydratase deficiency","type":"related"}],"termid":"MONDO:0014563","xrefs":{"Monarch":{"xref_id":"0014563"}}}


id: PBO:0041466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 10 open reading frame 126","termid":"PBO:0041466"}


id: FYPO:0003896
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of the mitochondrion is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitochondrion","termid":"FYPO:0006034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal mitochondrial morphology","synonyms":[{"name":"normal mitochondrial morphology during mitotic cell cycle","type":"related"},{"name":"normal mitochondrial morphology during vegetative growth","type":"exact"},{"name":"normal mitochondrial tubular network morphology","type":"exact"}],"termid":"FYPO:0003896"}


id: GO:0045884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of survival gene product expression; survival gene products are those that antagonize the apoptotic program. Regulation can be at the transcriptional, translational, or posttranslational level.","definition_xrefs":["GOC:mtg_apoptosis","GOC:dph","GOC:go_curators","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of survival gene product expression (obsolete GO:0045884)","synonyms":[{"name":"regulation of survival gene product activity","type":"broad"},{"name":"regulation of survival gene product expression","type":"exact"},{"name":"regulation of survival gene products","type":"broad"}],"termid":"GO:0045884"}


id: GO:1905662
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of telomerase RNA reverse transcriptase activity.","definition_xrefs":["PMID:22633954","GOC:TermGenie","GOC:nc","GOC:BHF_telomere","GOC:BHF","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of telomerase RNA reverse transcriptase activity (obsolete GO:1905662)","synonyms":[{"name":"down regulation of telomerase RNA reverse transcriptase activity","type":"exact"},{"name":"down regulation of telomerase, catalyst","type":"exact"},{"name":"down-regulation of telomerase RNA reverse transcriptase activity","type":"exact"},{"name":"down-regulation of telomerase, catalyst","type":"exact"},{"name":"downregulation of telomerase RNA reverse transcriptase activity","type":"exact"},{"name":"downregulation of telomerase, catalyst","type":"exact"},{"name":"inhibition of telomerase RNA reverse transcriptase activity","type":"narrow"},{"name":"inhibition of telomerase, catalyst","type":"narrow"},{"name":"negative regulation of telomerase, catalyst","type":"exact"}],"termid":"GO:1905662"}


id: PBO:0117092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKCE antisense RNA 2","termid":"PBO:0117092"}


id: MONDO:0958127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bronchiolitis obliterans syndrome","termid":"MONDO:0015265"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transplant-related bronchiolitis obliterans","secondary_identifiers":["Orphanet:658602","MEDGEN:1808244","UMLS:C5574736"],"termid":"MONDO:0958127","xrefs":{"Monarch":{"xref_id":"0958127"}}}


id: PBO:0026769
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_cell_surface","termid":"PBO:0026769"}


id: PBO:0079150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspanin 11","termid":"PBO:0079150"}


id: PBO:0001585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-ZZ type","termid":"PBO:0001585"}


id: GO:0044628
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of complement activation by the classical pathway, in a different organism.","definition_xrefs":["GOC:jl","PMID:20837040"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of complement activation, classical pathway in another organism (obsolete GO:0044628)","synonyms":[{"name":"positive regulation of complement activation, classical pathway in other organism","type":"exact"}],"termid":"GO:0044628"}


id: PR:000050546
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GTP-binding protein gtr2 (Schizosaccharomyces pombe) that is non-covalently bound to GTP.","definition_xrefs":["PomBase:VW","PPRO:DAN","PMID:27227887"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"},{"relation_name":"is_a","term_name":"GTP-binding protein gtr2 (Schizosaccharomyces pombe)","termid":"PR:000050544"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gtr2/GTP+","pombase_gene_id":"SPCC777.05","synonyms":[{"name":"PomBase_original_PRO_term_name: GTP-binding protein gtr2, GTP-bound form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-gtr2/GTP+","type":"exact"},{"name":"gtr2/GTP+","type":"exact"},{"name":"Gtr2/GTP+","type":"exact"}],"termid":"PR:000050546"}


id: MONDO:0100421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly GATA1 gene mutation. (A change in the nucleotide sequence of the GATA1 gene.)","definition_xrefs":["NCIT:C82340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia, GATA1 gene mutation","synonyms":[{"name":"AML, ERYF1 Gene Mutation","type":"exact"},{"name":"AML, GATA Binding Protein 1 Gene Mutation","type":"exact"},{"name":"AML, GATA-1 Gene Mutation","type":"exact"},{"name":"AML, GATA1 Mutation","type":"exact"},{"name":"AML, GATA1 gene mutation","type":"exact"},{"name":"AML, GF-1 Gene Mutation","type":"exact"},{"name":"AML, GF1 Gene Mutation","type":"exact"},{"name":"AML, NF-E1 Gene Mutation","type":"exact"},{"name":"AML, NFE1 Gene Mutation","type":"exact"}],"termid":"MONDO:0100421","xrefs":{"Monarch":{"xref_id":"0100421"}}}


id: GO:0019889
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving pteridine, pyrazino(2,3-dipyrimidine), the parent structure of pterins and the pteroyl group.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pteridine-containing compound metabolic process","termid":"GO:0042558"}],"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":"pteridine metabolic process","synonyms":[{"name":"pteridine metabolism","type":"exact"}],"termid":"GO:0019889"}


id: MONDO:0010945
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the CA4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 17","secondary_identifiers":["DOID:0110404","ICD10CM:H35.5","OMIM:600852","GARD:10387","MEDGEN:322153","UMLS:C1833245","MESH:C563437"],"synonyms":[{"name":"CA4 retinitis pigmentosa","type":"exact"},{"name":"RP 17","type":"related"},{"name":"RP17","type":"exact"},{"name":"retinitis pigmentosa 17","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in CA4","type":"exact"},{"name":"retinitis pigmentosa type 17","type":"exact"}],"termid":"MONDO:0010945","xrefs":{"Monarch":{"xref_id":"0010945"}}}


id: PBO:0072393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS27A pseudogene 19","termid":"PBO:0072393"}


id: MONDO:0008946
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":"cerebral angiopathy, dysphoric","secondary_identifiers":["UMLS:C1859283","MEDGEN:349128","OMIM:213500","MESH:C565864"],"synonyms":[{"name":"cerebral angiopathy, dysphoric","type":"exact"}],"termid":"MONDO:0008946","xrefs":{"Monarch":{"xref_id":"0008946"}}}


id: PBO:0044035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CSPG4 pseudogene 4 Y-linked","termid":"PBO:0044035"}


id: GO:0071899
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of estrogen receptor binding, interacting selectively with an estrogen receptor.","definition_xrefs":["GOC:mah","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of estrogen receptor binding (obsolete GO:0071899)","termid":"GO:0071899"}


id: MONDO:0023153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type of abdominal tuberculosis that is characterized by accumulation of fluid in the abdomen, a swollen abdomen, and slightly raised tubercles of 1–2 mm all over the peritoneum.","definition_xrefs":["doi:10.5772/intechopen.70417"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"tuberculosis","termid":"MONDO:0018076"},{"relation_name":"is_a","term_name":"abdominal tuberculosis","termid":"MONDO:0000369"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tuberculous ascites","secondary_identifiers":["NCIT:C27076","MEDGEN:78815","SCTID:4501007","UMLS:C0275919","icd11.foundation:1747509566"],"synonyms":[{"name":"tuberculous ascites","type":"exact"}],"termid":"MONDO:0023153","xrefs":{"Monarch":{"xref_id":"0023153"}}}


id: PBO:0039622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annexin A5","termid":"PBO:0039622"}


id: PBO:0090197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [4Fe-4S] cluster transfer protein Uvi31","termid":"PBO:0090197"}


id: PBO:0079529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-yW synthesizing protein 3 homolog","termid":"PBO:0079529"}


id: PBO:0082206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha1,2-mannosyltransferase of the Golgi; involved in protein mannosylation; KRE2 has a paralog, KTR6, that arose from the whole genome duplication","termid":"PBO:0082206"}


id: PR:O13688
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nse6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13688"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-structural maintenance of chromosome element 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11E3.08c","synonyms":[{"name":"Spom972h-nse6","type":"exact"},{"name":"core protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"non-SMC element 6 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13688"}


id: PBO:0076147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUN domain containing ossification factor","termid":"PBO:0076147"}


id: GO:0019674
data:
  {"annotated_genes":["SJAG_03091","SJAG_00714","SJAG_03946","SJAG_02889","SJAG_01566","SJAG_01753","SJAG_01500","SJAG_00522","SJAG_02191","SJAG_03298","SJAG_04693","SJAG_02154","SJAG_03306","SJAG_02618","SJAG_01582"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58756,68129,70745],"is_not":false,"summary":null,"term":"GO:0019674"},{"annotations":[98485,89710,118581,113815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043490"},{"annotations":[76524,79434,115097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009435"},{"annotations":[72566,81870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034355"},{"annotations":[74157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019677"},{"annotations":[97020,97021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006735"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving nicotinamide adenine dinucleotide (NAD+), a coenzyme that interconverts with its reduced form, NADH, in many redox and catabolic reactions.","definition_xrefs":["PMID:28648096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide metabolic process","termid":"GO:0006163"},{"relation_name":"is_a","term_name":"nicotinamide nucleotide metabolic process","termid":"GO:0046496"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00522":null,"SJAG_00714":null,"SJAG_01500":null,"SJAG_01566":null,"SJAG_01582":null,"SJAG_01753":null,"SJAG_02154":null,"SJAG_02191":null,"SJAG_02618":null,"SJAG_02889":null,"SJAG_03091":null,"SJAG_03298":null,"SJAG_03306":null,"SJAG_03946":null,"SJAG_04693":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"NAD+ metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-196807"],"synonyms":[{"name":"NAD (oxidized) metabolic process","type":"exact"},{"name":"NAD (oxidized) metabolism","type":"exact"},{"name":"NAD metabolic process","type":"exact"},{"name":"NAD metabolism","type":"exact"},{"name":"NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"oxidized NAD metabolic process","type":"exact"},{"name":"oxidized NAD metabolism","type":"exact"},{"name":"oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"}],"termid":"GO:0019674","terms_by_termid":{"GO:0006735":null,"GO:0009435":null,"GO:0019674":null,"GO:0019677":null,"GO:0034355":null,"GO:0043490":null}}


id: MONDO:0019361
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete boutonneuse fever (obsolete MONDO:0019361)","termid":"MONDO:0019361","xrefs":{"Monarch":{"xref_id":"0019361"}}}


id: GO:0051907
data:
  {"annotated_genes":["SJAG_05256"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97448],"is_not":false,"summary":null,"term":"GO:0051907"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-(hydroxymethyl)glutathione = formaldehyde + glutathione.","definition_xrefs":["RHEA:22488","EC:4.4.1.22"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05256":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"S-(hydroxymethyl)glutathione synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["UM-BBD_reactionID:r1145","KEGG_REACTION:R06982","MetaCyc:RXN-2961"],"synonyms":[{"name":"Gfa","type":"related"},{"name":"S-(hydroxymethyl)glutathione formaldehyde-lyase (glutathione-forming)","type":"related"},{"name":"S-(hydroxymethyl)glutathione formaldehyde-lyase activity","type":"related"},{"name":"glutathione-dependent formaldehyde-activating enzyme activity","type":"exact"}],"termid":"GO:0051907","terms_by_termid":{"GO:0051907":null}}


id: MONDO:0002381
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm arising from the sweat glands.","definition_xrefs":["NCIT:C3398"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal appendage tumor","termid":"MONDO:0002297"},{"relation_name":"is_a","term_name":"sweat gland disorder","termid":"MONDO:0006615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"sweat gland neoplasm","secondary_identifiers":["ICD9:239.2","EFO:1001204","SCTID:126490003","MEDGEN:21039","ICDO:8400/1","MONDO:0021219","UMLS:C0038987","MESH:D013544","DOID:2664"],"synonyms":[{"name":"neoplasm of sweat gland","type":"exact"},{"name":"neoplasm of the sweat gland","type":"exact"},{"name":"sweat gland neoplasm","type":"exact"},{"name":"sweat gland neoplasm (disease)","type":"exact"},{"name":"sweat gland neoplasms","type":"exact"},{"name":"sweat gland tumor","type":"exact"},{"name":"sweat gland tumor (morphologic abnormality)","type":"exact"},{"name":"sweat gland tumor NOS (morphologic abnormality)","type":"exact"},{"name":"sweat gland tumour","type":"exact"},{"name":"sweat gland tumour (morphologic abnormality)","type":"exact"},{"name":"sweat gland tumour NOS (morphologic abnormality)","type":"exact"},{"name":"tumor of sweat gland","type":"exact"},{"name":"tumor of the sweat gland","type":"exact"},{"name":"tumour of sweat gland","type":"exact"},{"name":"tumour of the sweat gland","type":"exact"}],"termid":"MONDO:0002381","xrefs":{"Monarch":{"xref_id":"0002381"}}}


id: PBO:0042888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 410","termid":"PBO:0042888"}


id: PBO:0091999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein P1 Rpp103","termid":"PBO:0091999"}


id: PBO:0063476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein disulfide isomerase family A member 4","termid":"PBO:0063476"}


id: PBO:0111911
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-AN1 type","termid":"PBO:0111911"}


id: PBO:0031367
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_DNA_recombination","termid":"PBO:0031367"}


id: PBO:0028434
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_superoxide_dismutase_activity","termid":"PBO:0028434"}


id: PR:P87303
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A general transcription factor IIH subunit 4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03841","PANTHER:PTHR13152:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II transcription factor B subunit 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC13G1.13","secondary_identifiers":["UniProtKB:P87303"],"synonyms":[{"name":"RNA polymerase II transcription factor B 52 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerase II transcription factor B p52 subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-GTF2H4","type":"exact"}],"termid":"PR:P87303"}


id: FYPO:0005605
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 sites at which the protein Ssb1 accumulates remain present for longer than normal during a cellular response to ionizing radiation.","definition_xrefs":["PomBase:mah","PMID:27098497"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"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"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased duration of Ssb1 focus presence during cellular response to ionizing radiation","synonyms":[{"name":"delayed peak level of Ssb1 foci","type":"related"},{"name":"increased duration of RPA focus presence during cellular response to ionizing radiation","type":"exact"},{"name":"increased duration of Rad11 focus presence during cellular response to ionizing radiation","type":"exact"},{"name":"increased duration of Rpa1 focus presence during cellular response to ionizing radiation","type":"exact"},{"name":"increased duration of Ssb1 focus presence during cellular response to ionizing radiation during mitotic cell cycle","type":"related"},{"name":"increased duration of Ssb1 focus presence during cellular response to ionizing radiation during vegetative growth","type":"exact"},{"name":"increased persistence of Ssb1 foci during cellular response to ionizing radiation","type":"exact"},{"name":"prolonged Ssb1 focus presence during cellular response to ionizing radiation","type":"exact"}],"termid":"FYPO:0005605"}


id: MONDO:0019291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic dermis disorder (obsolete MONDO:0019291)","secondary_identifiers":["Orphanet:79377"],"synonyms":[{"name":"dermis disorder","type":"related"}],"termid":"MONDO:0019291","xrefs":{"Monarch":{"xref_id":"0019291"}}}


id: MONDO:0006570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A long-term skin condition that mainly affects the skin of the genitals. It usually causes itching and white patches to appear on the affected skin.","definition_xrefs":["EFO:1000724"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"lichen disease","secondary_identifiers":["ICD9:697.9","MEDGEN:507920","SCTID:88996004","DOID:8574","ICD9:697","UMLS:C0023643","ICD9:697.8"],"synonyms":[{"name":"lichen","type":"exact"},{"name":"lichen condition","type":"related"}],"termid":"MONDO:0006570","xrefs":{"Monarch":{"xref_id":"0006570"}}}


id: MONDO:0001637
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"entropion","termid":"MONDO:0001519"}],"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":"cicatricial entropion","secondary_identifiers":["MEDGEN:509840","UMLS:C0155191","DOID:13113","SCTID:67383002","ICD9:374.04"],"termid":"MONDO:0001637","xrefs":{"Monarch":{"xref_id":"0001637"}}}


id: PBO:0031574
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-small_vegetative_cell","termid":"PBO:0031574"}


id: GO:0090475
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any protein processing achieved by the cleavage of a peptide bond after two consecutive lysine amino acid residues within a protein.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dibasic protein processing","termid":"GO:0090472"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051604","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"lys-lys specific dibasic protein processing","termid":"GO:0090475"}


id: GO:0044167
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding the host cell endoplasmic reticulum.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell membrane","termid":"GO:0033644"},{"relation_name":"part_of","term_name":"host cell endomembrane system","termid":"GO:0033645"},{"relation_name":"part_of","term_name":"host cell endoplasmic reticulum","termid":"GO:0044165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell endoplasmic reticulum membrane","synonyms":[{"name":"host endoplasmic reticulum membrane","type":"exact"}],"termid":"GO:0044167"}


id: PBO:0070365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY5 pseudogene 3","termid":"PBO:0070365"}


id: MONDO:0024551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, primary immunodeficiency disorder characterized by an abnormal immune response to Epstein-Barr virus (EBV) infection, caused by hemizygous mutations in the X-linked SH2D1A gene, resulting in B cell lymphoproliferation and manifesting with various phenotypes which include EBV-driven severe or fulminant mononucleosis, hemophagocytic lymphohistiocytosis (presenting with fulminant hepatitis, hepatic necrosis, bone marrow hypoplasia, and neurological involvement), hypogammaglobulinemia, and B-cell lymphoma. Additional variable manifestations include vasculitis, lymphomatoid granulomatosis, aplastic anemia, and chronic gastritis. Occasionally, T-cell lymphoma may be observed. Laboratory findings include normal or increased activated T cells and reduced memory B cells.","definition_xrefs":["Orphanet:538931"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked lymphoproliferative syndrome","termid":"MONDO:0010627"},{"relation_name":"is_a","term_name":"X-linked recessive disease","termid":"MONDO:0020605"}],"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":"X-linked lymphoproliferative disease due to SH2D1A deficiency","secondary_identifiers":["UMLS:C5399825","OMIM:308240","GARD:7906","MEDGEN:1770239"],"synonyms":[{"name":"Duncan disease","type":"related"},{"name":"EBV infection, Severe, susceptibility to","type":"related"},{"name":"Epstein-Barr Virus infection, familial fatal","type":"related"},{"name":"Lyp","type":"related"},{"name":"Purtilo syndrome","type":"related"},{"name":"X-linked lymphoproliferative disease due to SH2D1A deficiency","type":"exact"},{"name":"XLP1","type":"related"},{"name":"Xlp","type":"related"},{"name":"immunodeficiency 5","type":"related"},{"name":"immunodeficiency, X-linked progressive combined variable","type":"related"},{"name":"infectious mononucleosis, Severe, susceptibility to","type":"related"},{"name":"lymphoproliferative disease, X-linked","type":"related"},{"name":"lymphoproliferative syndrome, X-linked, 1","type":"related"},{"name":"lymphoproliferative syndrome, X-linked, 1, X-linked recessive","type":"exact"}],"termid":"MONDO:0024551","xrefs":{"Monarch":{"xref_id":"0024551"}}}


id: MONDO:1012046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar cortical atrophy, non-human animal","termid":"MONDO:1011836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellar cortical atrophy, domestic cat","secondary_identifiers":["OMIA:000177-9685"],"termid":"MONDO:1012046","xrefs":{"Monarch":{"xref_id":"1012046"}}}


id: PBO:0067354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 452, pseudogene","termid":"PBO:0067354"}


id: SO:0000306
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A nucleotide modified by methylation.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_DNA_base","termid":"SO:0000305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylated_DNA_base_feature","synonyms":[{"name":"methylated base feature","type":"exact"}],"termid":"SO:0000306"}


id: PBO:0067467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 596, pseudogene","termid":"PBO:0067467"}


id: GO:1901797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of signal transduction by p53 class mediator.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction by p53 class mediator","termid":"GO:1901796"},{"relation_name":"is_a","term_name":"negative regulation of intracellular signal transduction","termid":"GO:1902532"},{"relation_name":"negatively_regulates","term_name":"signal transduction by p53 class mediator","termid":"GO:0072331"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of signal transduction by p53 class mediator","synonyms":[{"name":"down regulation of signal transduction by p53 class mediator","type":"exact"},{"name":"down-regulation of signal transduction by p53 class mediator","type":"exact"},{"name":"downregulation of signal transduction by p53 class mediator","type":"exact"},{"name":"inhibition of signal transduction by p53 class mediator","type":"narrow"}],"termid":"GO:1901797"}


id: GO:0071423
data:
  {"annotated_genes":["SJAG_02140","SJAG_01406"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68911],"is_not":false,"summary":null,"term":"GO:0071423"},{"annotations":[103599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098714"}]},"cv_name":"biological_process","definition":"A process in which a malate ion is transported across a membrane.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malate transport","termid":"GO:0015743"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01406":null,"SJAG_02140":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"malate transmembrane transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"malate membrane transport","type":"exact"},{"name":"transmembrane malate transport","type":"exact"}],"termid":"GO:0071423","terms_by_termid":{"GO:0071423":null,"GO:0098714":null}}


id: GO:0099605
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that regulates the frequency of action potentials in a spike train.","definition_xrefs":["ISBN:978-0071390118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of action potential","termid":"GO:0098900"}],"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 action potential firing rate","termid":"GO:0099605"}


id: MONDO:0005657
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aspergillosis is an infection, growth, or allergic response caused by the Aspergillus fungus. There are several different kinds of aspergillosis. One kind is allergic bronchopulmonary aspergillosis (also called ABPA), a condition where the fungus causes allergic respiratory symptoms similar to asthma, such as wheezing and coughing, but does not actually invade and destroy tissue. Another kind of aspergillosis is invasive aspergillosis. This infection usually affects people with weakened immune systems due to cancer, AIDS, leukemia, organ transplantation, chemotherapy, or other conditions or events that reduce the number of normal white blood cells. In this condition, the fungus invades and damages tissues in the body. Invasive aspergillosis most commonly affects the lungs, but can also cause infection in many other organs and can spread throughout the body (commonly affecting the kidneys and brain). Aspergilloma, a growth (fungus ball) that develops in an area of previous lung disease such as tuberculosis or lung abscess, is a third kind of aspergillosis. This type of aspergillosis is composed of a tangled mass of fungus fibers, blood clots, and white blood cells. The fungus ball gradually enlarges, destroying lung tissue in the process, but usually does not spread to other areas.","direct_ancestors":[{"relation_name":"is_a","term_name":"opportunistic mycosis","termid":"MONDO:0002312"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspergillosis","secondary_identifiers":["EFO:0007157","Orphanet:1163","ICD9:117.3","DOID:13564","SCTID:65553006","MESH:D001228","UMLS:C0004030","icd11.foundation:1913468488","MEDGEN:13939","ICD10CM:B44","MedDRA:10003488","CSP:1988-4002","GARD:5856","NCIT:C2886","NORD:814"],"synonyms":[{"name":"infection due to Aspergillus","type":"exact"}],"termid":"MONDO:0005657","xrefs":{"Monarch":{"xref_id":"0005657"}}}


id: MONDO:0013461
data:
  {"annotated_genes":["SJAG_03797"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88597],"is_not":false,"summary":null,"term":"MONDO:0013461"}]},"cv_name":"mondo","definition":"An inherited condition caused by mutation(s) in the ITPA gene, encoding inosine triphosphate pyrophosphatase. It is characterized by elevated concentrations of inosine triphosphate in erythrocytes.","definition_xrefs":["NCIT:C129974"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03797":null},"genotype_count":0,"is_obsolete":false,"name":"inosine triphosphatase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:238011005","UMLS:C0342800","ICD9:277.2","MEDGEN:452450","OMIM:613850","Orphanet:319684","MESH:C564127"],"synonyms":[{"name":"inosine triphosphatase deficiency","type":"exact"},{"name":"inosine triphosphate pyrophosphohydrolase deficiency","type":"related"}],"termid":"MONDO:0013461","terms_by_termid":{"MONDO:0013461":null},"xrefs":{"Monarch":{"xref_id":"0013461"}}}


id: PBO:0045052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deleted in lymphocytic leukemia 1","termid":"PBO:0045052"}


id: PR:O60158
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- bqt4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60158"],"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":"bouquet formation protein 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C7.10","synonyms":[{"name":"Spom972h-bqt4","type":"exact"}],"termid":"PR:O60158"}


id: PBO:0087377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STE20-family GCKIII protein kinase; required for prospore membrane closure, efficient spore packaging, and localization of enzymes involved in spore wall synthesis; component of a non-canonical Hippo pathway with Cdc15p involved in spindle disassembly and sustained release of Cdc14p during anaphase II; forms a complex with Cdc15p;  phosphorylation requires Cdc15p; required for Ssp1p phosphorylation and turnover; interacts with 14-3-3 proteins; expressed in late meiosis; nuclear and cytoplasmic","termid":"PBO:0087377"}


id: FYPO:0001945
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 protein secretion is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein transport during vegetative growth","termid":"FYPO:0004848"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000138"],"is_obsolete":false,"name":"normal protein secretion","synonyms":[{"name":"normal protein secretion during mitotic cell cycle","type":"related"},{"name":"normal protein secretion during vegetative growth","type":"exact"}],"termid":"FYPO:0001945"}


id: PBO:0034073
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_many_to_many_homology_relationship_with","termid":"PBO:0034073"}


id: MONDO:0015034
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lissencephaly with cerebellar hypoplasia type A (LCHa) is a form of lissencephaly with cerebellar hypoplasia that encompasses classical lissencephaly with thickened cortical gray matter with either no discernible gradient, a gradient with posterior predominance, or a gradient with anterior predominance, and cerebellar vermis hypoplasia.","definition_xrefs":["Orphanet:100011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lissencephaly with cerebellar hypoplasia","termid":"MONDO:0019450"}],"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":"lissencephaly with cerebellar hypoplasia type A","secondary_identifiers":["MEDGEN:1679234","GARD:19731","UMLS:C5191423","icd11.foundation:853428618"],"termid":"MONDO:0015034","xrefs":{"Monarch":{"xref_id":"0015034"}}}


id: RO:0002004
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"The relationship that holds between a trachea or tracheole and an antomical structure that is contained in (and so provides an oxygen supply to).","direct_ancestors":[{"relation_name":"is_a","term_name":"contained_in","termid":"RO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tracheates","termid":"RO:0002004"}


id: PBO:0050737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family E (Hsp10) member 1","termid":"PBO:0050737"}


id: GO:0098986
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A T-shaped presynpatic density. These are common in arhropod central nervous systems.","definition_xrefs":["GOC:dos","PMID:26780543"],"direct_ancestors":[{"relation_name":"is_a","term_name":"presynaptic density","termid":"GO:0098980"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005938"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005938"],"is_obsolete":false,"name":"T-bar","termid":"GO:0098986"}


id: PBO:0058714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6842","termid":"PBO:0058714"}


id: MONDO:0700019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which chromosome 12 is affected.","definition_xrefs":["MONDO:patterns/chromosome_type"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal anomaly","termid":"MONDO:0020049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 12 disorder","termid":"MONDO:0700019","xrefs":{"Monarch":{"xref_id":"0700019"}}}


id: GO:0009367
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. An enzyme complex that catalyzes the cleavage of a Gly-Phe bond to release an N-terminal, basic peptide of 5-8 residues from type IV prepilin, and then N-methylates the new N-terminal amino group.","definition_xrefs":["EC:3.4.23.43"],"gene_count":0,"genotype_count":0,"name":"obsolete prepilin peptidase complex (obsolete GO:0009367)","synonyms":[{"name":"prepilin peptidase complex","type":"exact"}],"termid":"GO:0009367"}


id: MONDO:1012130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin A deficiency, non-human animal","termid":"MONDO:1011726"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin A deficiency, dog","secondary_identifiers":["OMIA:000552-9615"],"termid":"MONDO:1012130","xrefs":{"Monarch":{"xref_id":"1012130"}}}


id: PR:000085730
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.2, initiator methionine removed form (Schizosaccharomyces pombe) that has been methylated on Lys-9 but not phosphorylated on Ser-10. Example: UniProtKB:P09988, 2-136, Lys-10, MOD:00663|Ser-11, PR:000026291.","definition_xrefs":["PRO:DAN","PomBase:VW","PMID:19362535"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3.2, initiator methionine removed form (Schizosaccharomyces pombe)","termid":"PR:000027580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hht2/Me:(K9),UnPhos(S10)","pombase_gene_id":"SPBC8D2.04","synonyms":[{"name":"PRO_0000221366, Lys-10, MOD:00663|Ser-11, PR:000026291","type":"related"},{"name":"PomBase_original_PRO_term_name: histone H3.2, initiator methionine removed K9-methylated and unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hht2/InitMet-/K9MeUnPhos:1","type":"exact"},{"name":"UniProtKB:P09988, 2-136, Lys-10, MOD:00663|Ser-11, PR:000026291","type":"related"},{"name":"hht2/Me:(K9),UnPhos(S10)","type":"exact"}],"termid":"PR:000085730"}


id: PBO:0055884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 8 VRAC subunit B","termid":"PBO:0055884"}


id: GO:0071568
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of UFM1 from one protein to another via the reaction X-UFM1 + Y = Y-UFM1 + X, where both X-UFM1 and Y-UFM1 are covalent linkages.","definition_xrefs":["GOC:sp","PMID:20018847"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein transferase activity","termid":"GO:0019787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0019787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0019787","GO:0003674","GO:0016740","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"UFM1 transferase activity","termid":"GO:0071568"}


id: MONDO:0016458
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The newly described 8q12 microduplication syndrome is associated with unusual and characteristic multi-organ clinical features, which include hearing loss, congenital heart defects, intellectual disability, hypotonia in infancy, and Duane anomaly.","definition_xrefs":["Orphanet:228399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 8","termid":"MONDO:0016959"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"8q12 microduplication syndrome","secondary_identifiers":["GARD:12816","SCTID:719684000","UMLS:C4304504","MEDGEN:930173"],"synonyms":[{"name":"chromosome 8q12 microduplication syndrome","type":"related"},{"name":"dup(8)(q12)","type":"exact"},{"name":"trisomy 8q12","type":"exact"}],"termid":"MONDO:0016458","xrefs":{"Monarch":{"xref_id":"0016458"}}}


id: PBO:0040458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase 13A1","termid":"PBO:0040458"}


id: FYPO:0004788
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype in which the phosphorylation of serine residues in one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal when the cell is subject to glucose starvation.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete increased protein serine phosphorylation during glucose starvation (obsolete FYPO:0004788)","synonyms":[{"name":"increased peptidyl-serine phosphorylation during glucose starvation","type":"exact"},{"name":"increased protein serine phosphorylation during cellular response to glucose starvation","type":"exact"},{"name":"increased protein serine phosphorylation during glucose depletion","type":"exact"},{"name":"increased protein serine phosphorylation during glucose deprivation","type":"exact"},{"name":"increased protein serine phosphorylation during glucose limitation","type":"related"},{"name":"increased serine phosphorylation during glucose starvation","type":"exact"}],"termid":"FYPO:0004788"}


id: GO:0001775
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A multicellular organismal process by which exposure to an activating factor such as a cellular or soluble ligand results in a change in the morphology or behavior of a cell.","definition_xrefs":["GOC:mgi_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"},{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"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 activation","termid":"GO:0001775"}


id: GO:0021778
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into an oligodendrocyte in an environment that is neutral with respect to the developmental pathway. Upon specification, the cell fate can be reversed.","definition_xrefs":["GOC:dph","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell fate specification","termid":"GO:0021780"},{"relation_name":"part_of","term_name":"oligodendrocyte cell fate commitment","termid":"GO:0021779"}],"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":"oligodendrocyte cell fate specification","termid":"GO:0021778"}


id: MONDO:0020207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare isolated myopia is a rare, genetic, refraction anomaly disorder characterized by non-syndromic severe myopia, which may be associated with cataract and vitreoretinal degeneration (retinal detachment) that may lead to blindness.","definition_xrefs":["Orphanet:98619"],"gene_count":0,"genotype_count":0,"name":"obsolete rare isolated myopia (obsolete MONDO:0020207)","termid":"MONDO:0020207","xrefs":{"Monarch":{"xref_id":"0020207"}}}


id: GO:0034212
data:
  {"annotated_genes":["SJAG_04791","SJAG_01204","SJAG_00676","SJAG_01826","SJAG_02773","SJAG_02990","SJAG_03537","SJAG_02165","SJAG_04631","SJAG_04131","SJAG_02726","SJAG_03900"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[66536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004402"},{"annotations":[75796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043998"},{"annotations":[92639,93303],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036408"},{"annotations":[93304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043993"},{"annotations":[100894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044016"},{"annotations":[74345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032931"},{"annotations":[93305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043992"},{"annotations":[100895,75798],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010485"},{"annotations":[90300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043997"},{"annotations":[90301],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043995"},{"annotations":[90302],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043996"},{"annotations":[117367,105531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120518"},{"annotations":[79141,75799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990189"},{"annotations":[105942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061733"},{"annotations":[120025],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004596"},{"annotations":[91276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008999"},{"annotations":[79142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990190"}]},"cv_name":"molecular_function","definition":"Catalysis of the acetylation of an amino acid residue of a peptide or protein, according to the reaction: acetyl-CoA + peptide = CoA + N-acetylpeptide.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetyltransferase activity","termid":"GO:0008080"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00676":null,"SJAG_01204":null,"SJAG_01826":null,"SJAG_02165":null,"SJAG_02726":null,"SJAG_02773":null,"SJAG_02990":null,"SJAG_03537":null,"SJAG_03900":null,"SJAG_04131":null,"SJAG_04631":null,"SJAG_04791":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"protein N-acetyltransferase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9760081","Reactome:R-HSA-3371554"],"synonyms":[{"name":"RHEA:45948","type":"broad"},{"name":"peptide N-acetyltransferase activity","type":"exact"}],"termid":"GO:0034212","terms_by_termid":{"GO:0004402":null,"GO:0004596":null,"GO:0008999":null,"GO:0010485":null,"GO:0032931":null,"GO:0036408":null,"GO:0043992":null,"GO:0043993":null,"GO:0043995":null,"GO:0043996":null,"GO:0043997":null,"GO:0043998":null,"GO:0044016":null,"GO:0061733":null,"GO:0120518":null,"GO:1990189":null,"GO:1990190":null}}


id: RO:0002337
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship that holds via some process of localization","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"related_via_localization_to","termid":"RO:0002337"}


id: PBO:0000589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcineurin responsive transcription factor Prz1","termid":"PBO:0000589"}


id: MONDO:0000979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An endemic bacterial infection caused by Treponema carateum. It is manifested with chronic cutaneous lesions. The early lesions consist of papules and erythematous plaques. The late lesions consist of hypochromic, achromic, hyperpigmented and atrophic lesions. The late skin lesions may cause destruction of bones and cartilage and produce disfiguring changes.","definition_xrefs":["NCIT:C85011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"Treponema infectious disease","termid":"MONDO:0007000"},{"relation_name":"is_a","term_name":"skin disease caused by bacterial infection","termid":"MONDO:0024295"}],"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":"pinta disease","secondary_identifiers":["ICD9:103","ICD9:103.0","ICD9:103.1","ICD9:103.3","ICD9:103.9","DOID:1022","MESH:D010874","NORD:1580","SCTID:22064009","UMLS:C0031946","MEDGEN:45926","ICD9:103.2"],"synonyms":[{"name":"Azul","type":"related"},{"name":"Carate","type":"related"},{"name":"Empeines","type":"related"},{"name":"Lota","type":"related"},{"name":"Mal del pinto","type":"related"},{"name":"Pinta","type":"exact"},{"name":"Tina","type":"related"},{"name":"endemic treponematosis caused by Treponema carateum","type":"related"},{"name":"infection by Treponema carateum","type":"related"},{"name":"pinta","type":"exact"}],"termid":"MONDO:0000979","xrefs":{"Monarch":{"xref_id":"0000979"}}}


id: GO:0042382
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Discrete subnuclear bodies in the interchromatin nucleoplasmic space, often located adjacent to nuclear specks. 10-20 paraspeckles are typically found in human cell nuclei.","definition_xrefs":["PMID:11790299","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear ribonucleoprotein granule","termid":"GO:0140168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005654","GO:0005634"],"is_obsolete":false,"name":"paraspeckles","secondary_identifiers":["Wikipedia:Paraspeckle"],"termid":"GO:0042382"}


id: GO:1902136
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving (-)-secoisolariciresinol.","definition_xrefs":["PMID:9872995","GOC:TermGenie","PMID:8910615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan metabolic process","termid":"GO:0009806"},{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"diol metabolic process","termid":"GO:0034311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"(-)-secoisolariciresinol metabolic process","synonyms":[{"name":"(-)-secoisolariciresinol metabolism","type":"exact"}],"termid":"GO:1902136"}


id: MONDO:1010981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hydranencephaly that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydranencephaly, non-human animal","termid":"MONDO:1010232"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydranencephaly, sheep","secondary_identifiers":["OMIA:000486-9940"],"termid":"MONDO:1010981","xrefs":{"Monarch":{"xref_id":"1010981"}}}


id: PBO:0059169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myelin protein zero","termid":"PBO:0059169"}


id: MONDO:0007840
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":"internal carotid artery, spontaneous dissection of","secondary_identifiers":["MESH:C564125","OMIM:147820","MEDGEN:333477","UMLS:C1840073"],"synonyms":[{"name":"internal carotid artery, spontaneous dissection of","type":"exact"}],"termid":"MONDO:0007840","xrefs":{"Monarch":{"xref_id":"0007840"}}}


id: PBO:0053034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LARGE intronic transcript 1","termid":"PBO:0053034"}


id: PBO:0089937
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WW domain protein Wwm1","termid":"PBO:0089937"}


id: GO:0001324
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. 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.) occurring in non-dividing cells as they age as a result of oxidative stress, where the change varies according to the age of the cell or organism.","definition_xrefs":["GOC:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete age-dependent response to oxidative stress involved in chronological cell aging (obsolete GO:0001324)","synonyms":[{"name":"age-dependent response to oxidative stress during chronological cell ageing","type":"related"},{"name":"age-dependent response to oxidative stress during chronological cell aging","type":"related"}],"termid":"GO:0001324"}


id: PBO:0038717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin gamma 1 pseudogene 12","termid":"PBO:0038717"}


id: GO:0019391
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glucuronosides, compound composed of a hydroxy compound linked to a glucuronate residue.","definition_xrefs":["PMID:28389557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoside catabolic process","termid":"GO:0016139"}],"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":"glucuronoside catabolic process","secondary_identifiers":["MetaCyc:GLUCUROCAT-PWY"],"synonyms":[{"name":"glucuronide catabolic process","type":"exact"},{"name":"glucuronide catabolism","type":"exact"},{"name":"glucuronoside breakdown","type":"exact"},{"name":"glucuronoside catabolism","type":"exact"},{"name":"glucuronoside degradation","type":"exact"}],"termid":"GO:0019391"}


id: PBO:0045642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox A","termid":"PBO:0045642"}


id: PR:O94669
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- apm3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94669"],"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":"AP-3 complex subunit mu (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC651.11c","synonyms":[{"name":"Spom972h-apm3","type":"exact"},{"name":"adaptor-related protein complex 3 subunit mu (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94669"}


id: PR:Q9UTN4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pfs2 gene.","definition_xrefs":["UniProtKB:Q9UTN4","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyadenylation factor subunit 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC12G12.14c","synonyms":[{"name":"Spom972h-pfs2","type":"exact"}],"termid":"PR:Q9UTN4"}


id: GO:0009729
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a brassinosteroid stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of hormone stimulus","termid":"GO:0009720"},{"relation_name":"is_a","term_name":"response to brassinosteroid","termid":"GO:0009741"}],"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 brassinosteroid stimulus","synonyms":[{"name":"perception of brassinosteroid stimulus","type":"related"}],"termid":"GO:0009729"}


id: GO:0048580
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of post-embryonic development. Post-embryonic development is defined as the process whose specific outcome is the progression of the organism over time, from the completion of embryonic development to the mature structure.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal development","termid":"GO:2000026"},{"relation_name":"regulates","term_name":"post-embryonic development","termid":"GO:0009791"}],"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 post-embryonic development","termid":"GO:0048580"}


id: _global:regulates_o_results_in_movement_of
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","definition":"A relation that holds between a process that regulates locomotion and the cell or organism whose locomotion is being regulated.","definition_xrefs":["GOC:dph","GOC:mtg_berkeley_2012_08_27","GOC:cjm"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulates_process_that_results_in_movement_of","secondary_identifiers":["GOREL:0001005"],"synonyms":[{"name":"regulates_o_results_in_movement_of","type":"exact"}],"termid":"_global:regulates_o_results_in_movement_of"}


id: PATO:0002154
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curvature quality inhering in a bearer by virtue of the bearer's being curved outwards the abdomen of an organism.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"splayed","termid":"PATO:0001785"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splayed ventral","synonyms":[{"name":"splayed anterior (human torso)","type":"exact"},{"name":"splayed inferior (human head)","type":"exact"}],"termid":"PATO:0002154"}


id: FYPO:0007148
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to transplatin. Cells stop growing (and may die) at a concentration of transplatin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002683","FYPO:0001985","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to transplatin","synonyms":[{"name":"hypersensitive to transplatin","type":"exact"},{"name":"sensitive to transplatin during mitotic cell cycle","type":"related"},{"name":"sensitive to v during vegetative growth","type":"exact"}],"termid":"FYPO:0007148"}


id: FYPO:0003702
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of the microtubule cytoskeleton is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal microtubule cytoskeleton morphology during vegetative growth","synonyms":[{"name":"normal microtubule cytoskeleton morphology during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003702"}


id: PBO:0077261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane p24 trafficking protein 10 pseudogene 1","termid":"PBO:0077261"}


id: PBO:0111932
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIT family","termid":"PBO:0111932"}


id: GO:0051060
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1,6)-alpha-D-glucosidic linkages in pullulan (a linear polymer of alpha-(1,6)-linked maltotriose units) and in amylopectin and glycogen, and the a- and b-limit dextrins of amylopectin and glycogen.","definition_xrefs":["EC:3.2.1.41"],"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:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824","GO:0016798"],"is_obsolete":false,"name":"pullulanase activity","secondary_identifiers":["MetaCyc:RXN-1824"],"synonyms":[{"name":"R-enzyme","type":"related"},{"name":"alpha-dextrin endo-1,6-alpha-glucosidase activity","type":"exact"},{"name":"amylopectin 6-glucanohydrolase activity","type":"exact"},{"name":"bacterial debranching enzyme","type":"related"},{"name":"debranching enzyme activity","type":"broad"},{"name":"limit dextrinase","type":"related"},{"name":"pullulan 6-glucanohydrolase activity","type":"exact"},{"name":"pullulan alpha-1,6-glucanohydrolase activity","type":"related"}],"termid":"GO:0051060"}


id: PBO:0067919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 221","termid":"PBO:0067919"}


id: PBO:0089505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA adenine glycosylase Myh1","termid":"PBO:0089505"}


id: GO:0098923
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell-cell signaling from postsynapse to presynapse, across the synaptic cleft, mediated by an soluble gas ligand.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retrograde trans-synaptic signaling","termid":"GO:0098917"},{"relation_name":"is_a","term_name":"trans-synaptic signaling by soluble gas","termid":"GO:0099543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"retrograde trans-synaptic signaling by soluble gas","termid":"GO:0098923"}


id: GO:0150022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an apical dendrite over time, from its formation to the mature structure.","definition_xrefs":["PMID:22683681","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite development","termid":"GO:0016358"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"apical dendrite development","termid":"GO:0150022"}


id: PBO:0065866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB23, member RAS oncogene family","termid":"PBO:0065866"}


id: PBO:0110106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi-specific 1-phosphatidylinositol 4-kinase, type III-beta Pik1","termid":"PBO:0110106"}


id: PBO:0081435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 286A","termid":"PBO:0081435"}


id: PBO:0056911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MER1 repeat containing imprinted transcript 1","termid":"PBO:0056911"}


id: PBO:0040130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASB15 antisense RNA 1","termid":"PBO:0040130"}


id: GO:0035348
data:
  {"annotated_genes":["SJAG_04325"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59920],"is_not":false,"summary":null,"term":"GO:0035348"}]},"cv_name":"biological_process","definition":"The process in which acetyl-CoA is transported across a membrane. Acetyl-CoA is a derivative of coenzyme A in which the sulfhydryl group is acetylated; it is a metabolite derived from several pathways (e.g. glycolysis, fatty acid oxidation, amino-acid catabolism) and is further metabolized by the tricarboxylic acid cycle. It is a key intermediate in lipid and terpenoid biosynthesis.","definition_xrefs":["GO:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetyl-CoA transport","termid":"GO:0015876"},{"relation_name":"is_a","term_name":"purine-containing compound transmembrane transport","termid":"GO:0072530"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04325":null},"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:0008150","GO:0006810","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"acetyl-CoA transmembrane transport","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"acetyl-CoA membrane transport","type":"exact"}],"termid":"GO:0035348","terms_by_termid":{"GO:0035348":null}}


id: MONDO:0020673
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Complete closure of the normally patent lumen of the blood vessels which carry blood away from the heart.","definition_xrefs":["NCIT:C35318"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arterial disorder","termid":"MONDO:0000473"},{"relation_name":"is_a","term_name":"vascular occlusion disorder","termid":"MONDO:0020672"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arterial occlusion","secondary_identifiers":["MEDGEN:78117","UMLS:C0264995"],"synonyms":[{"name":"arterial obstruction","type":"exact"},{"name":"arterial occlusion","type":"exact"}],"termid":"MONDO:0020673","xrefs":{"Monarch":{"xref_id":"0020673"}}}


id: MONDO:0005072
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuroblastoma (NB) is the most common solid, extracranial childhood tumor. It is an aggressive pediatric cancer that originates from neural crest tissues of the sympathetic nervous system.","definition_xrefs":["PMID:32903387"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autonomic nervous system neoplasm","termid":"MONDO:0002366"},{"relation_name":"excluded_subClassOf","term_name":"central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor","termid":"MONDO:0016713"},{"relation_name":"is_a","term_name":"neuroblastic tumor","termid":"MONDO:0006316"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroblastoma","secondary_identifiers":["NCIT:C3270","EFO:0000621","GARD:7185","MEDGEN:18012","SCTID:432328008","ICDO:9500/3","MESH:D009447","DOID:769","MedDRA:10029260","NANDO:2200040","ONCOTREE:NBL","Orphanet:635","NIFSTD:birnlex_12631","UMLS:C0027819"],"synonyms":[{"name":"NB","type":"related"},{"name":"neural Crest tumor, malignant","type":"exact"},{"name":"neuroblastoma","type":"exact"},{"name":"neuroblastoma (Schwannian Stroma-poor)","type":"exact"},{"name":"neuroblastoma, malignant","type":"exact"}],"termid":"MONDO:0005072","xrefs":{"Monarch":{"xref_id":"0005072"}}}


id: MONDO:0012801
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autism, susceptiblity to","termid":"MONDO:0020836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autism, susceptibility to, 15","secondary_identifiers":["MEDGEN:394302","UMLS:C2677504","OMIM:612100"],"synonyms":[{"name":"AUTS15","type":"related"},{"name":"autism susceptibility 15","type":"exact"},{"name":"autism, susceptibility to, 15","type":"exact"},{"name":"autism, susceptibility to, type 15","type":"exact"},{"name":"susceptibility to autism 15","type":"related"}],"termid":"MONDO:0012801","xrefs":{"Monarch":{"xref_id":"0012801"}}}


id: PBO:0002904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F1-ATPase alpha subunit","termid":"PBO:0002904"}


id: PBO:0055846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat, Ig-like and transmembrane domains 2","termid":"PBO:0055846"}


id: GO:0062098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of programmed necrotic cell death.","definition_xrefs":["GOC:rph","PMID:27258785","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of programmed cell death","termid":"GO:0043067"},{"relation_name":"regulates","term_name":"programmed necrotic cell death","termid":"GO:0097300"}],"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 programmed necrotic cell death","termid":"GO:0062098"}


id: PBO:0087484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of cleavage polyadenylation factor (CPF); interacts directly with poly(A) polymerase (Pap1p) to regulate its activity; bridging factor that links Pap1p and the CPF complex via Yth1p","termid":"PBO:0087484"}


id: MONDO:0005317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fatty liver (obsolete MONDO:0005317)","termid":"MONDO:0005317","xrefs":{"Monarch":{"xref_id":"0005317"}}}


id: GO:0045693
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of embryo sac central cell differentiation.","definition_xrefs":["GOC:go_curators","GOC:mtg_plant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of embryo sac central cell differentiation","termid":"GO:0045691"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"embryo sac central cell differentiation","termid":"GO:0009559"}],"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 embryo sac central cell differentiation","synonyms":[{"name":"activation of female gametophyte central cell differentiation","type":"narrow"},{"name":"positive regulation of female gametophyte central cell differentiation","type":"exact"},{"name":"stimulation of female gametophyte central cell differentiation","type":"narrow"},{"name":"up regulation of female gametophyte central cell differentiation","type":"exact"},{"name":"up-regulation of female gametophyte central cell differentiation","type":"exact"},{"name":"upregulation of female gametophyte central cell differentiation","type":"exact"}],"termid":"GO:0045693"}


id: PBO:0062551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily Q member 1","termid":"PBO:0062551"}


id: PBO:0088575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF3245 nucleolar protein, conserved in fungi and plant family","termid":"PBO:0088575"}


id: GO:1900010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of corticotropin-releasing hormone receptor activity.","definition_xrefs":["GOC:TermGenie","GOC:yaf","PMID:18234674"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of corticotropin-releasing hormone receptor activity (obsolete GO:1900010)","synonyms":[{"name":"regulation of CRF receptor activity","type":"exact"},{"name":"regulation of CRH receptor activity","type":"exact"},{"name":"regulation of adrenocorticotropin-releasing hormone receptor activity","type":"exact"},{"name":"regulation of corticotropin-releasing factor receptor activity","type":"exact"}],"termid":"GO:1900010"}


id: PBO:0015652
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-occupancy","termid":"PBO:0015652"}


id: PBO:0078614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 64E, pseudogene","termid":"PBO:0078614"}


id: MONDO:0017412
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete 2q31.1 microduplication syndrome (obsolete MONDO:0017412)","termid":"MONDO:0017412","xrefs":{"Monarch":{"xref_id":"0017412"}}}


id: PBO:0049697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan and proteoglycan link protein 3","termid":"PBO:0049697"}


id: MONDO:0012476
data:
  {"annotated_genes":["SJAG_00773"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86886],"is_not":false,"summary":null,"term":"MONDO:0012476"}]},"cv_name":"mondo","definition":"Autosomal spastic paraplegia type 30 (SPG30) is a form of hereditary spastic paraplegia characterized by either a pure spastic paraplegia phenotype, usually presenting in the first or second decade of life, with spastic lower extremities, usteady spastic gait, hyperreflexia and extensor plantar responses, or as a complicated phenotype with the additional manifestations of distal wasting, saccadic ocular movements, mild cerebellar ataxia and mild, distal, axonal neuropathy.","definition_xrefs":["Orphanet:101010"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"},{"relation_name":"is_a","term_name":"KIF1A related neurological disorder","termid":"MONDO:0700055"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00773":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 30","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:610357","MESH:C563677","UMLS:C5235139","SCTID:763377006","GARD:16942","MEDGEN:1710020","DOID:0110781"],"synonyms":[{"name":"KIF1A hereditary spastic paraplegia","type":"exact"},{"name":"SPG30","type":"exact"},{"name":"autosomal recessive spastic paraplegia 30","type":"exact"},{"name":"autosomal spastic paraplegia type 30","type":"exact"},{"name":"hereditary spastic paraplegia caused by mutation in KIF1A","type":"exact"},{"name":"hereditary spastic paraplegia type 30","type":"exact"},{"name":"spastic paraplegia 30, autosomal dominant","type":"exact"},{"name":"spastic paraplegia 30, autosomal recessive","type":"related"}],"termid":"MONDO:0012476","terms_by_termid":{"MONDO:0012476":null},"xrefs":{"Monarch":{"xref_id":"0012476"}}}


id: PBO:0066961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 263","termid":"PBO:0066961"}


id: PBO:0026755
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_transport_gene_mRNA_during_vegetative_growth","termid":"PBO:0026755"}


id: PBO:0059372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MRPS18C pseudogene 5","termid":"PBO:0059372"}


id: MONDO:0000215
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epilepsy, familial focal, with variable foci (obsolete MONDO:0000215)","termid":"MONDO:0000215","xrefs":{"Monarch":{"xref_id":"0000215"}}}


id: MONDO:0013100
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial atrial fibrillation","termid":"MONDO:0018054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"atrial fibrillation, familial, 8","secondary_identifiers":["MEDGEN:414420","GARD:15609","MESH:C567802","UMLS:C2751607","OMIM:613055"],"synonyms":[{"name":"ATFB8","type":"exact"},{"name":"atrial fibrillation, familial, 8","type":"exact"}],"termid":"MONDO:0013100","xrefs":{"Monarch":{"xref_id":"0013100"}}}


id: MONDO:0029136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"LAMA2-related muscular dystrophy","termid":"MONDO:0100228"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0006025"],"is_obsolete":false,"name":"muscular dystrophy, limb-girdle, autosomal recessive 23","secondary_identifiers":["UMLS:C4748327","GARD:22270","Orphanet:565837","MEDGEN:1648462","OMIM:618138"],"synonyms":[{"name":"LGMDR23","type":"related"},{"name":"laminin subunit alpha 2-related limb-girdle muscular dystrophy R23","type":"exact"},{"name":"muscular dystrophy, limb-girdle, autosomal recessive 23","type":"exact"}],"termid":"MONDO:0029136","xrefs":{"Monarch":{"xref_id":"0029136"}}}


id: GO:1903851
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cristae formation.","definition_xrefs":["GOC:pad","GO_REF:0000058","GOC:PARL","GOC:TermGenie","PMID:19279012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of organelle organization","termid":"GO:0010639"},{"relation_name":"is_a","term_name":"regulation of cristae formation","termid":"GO:1903850"},{"relation_name":"negatively_regulates","term_name":"cristae formation","termid":"GO:0042407"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007005"},{"rel_name":"regulates","termid":"GO:0007005"},{"rel_name":"negatively_regulates","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024","GO:0007005"],"is_obsolete":false,"name":"negative regulation of cristae formation","synonyms":[{"name":"down regulation of cristae formation","type":"exact"},{"name":"down-regulation of cristae formation","type":"exact"},{"name":"downregulation of cristae formation","type":"exact"},{"name":"inhibition of cristae formation","type":"narrow"}],"termid":"GO:1903851"}


id: PBO:0077987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon TGC) 9-1","termid":"PBO:0077987"}


id: MONDO:0015280
data:
  {"annotated_genes":["SJAG_00993","SJAG_02342","SJAG_01181","SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014112"},{"annotations":[86846,86844,86845],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014113"},{"annotations":[86851,86850,86849],"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:0005093"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005267"],"is_obsolete":false,"name":"cardiofaciocutaneous syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C535579","MEDGEN:266149","SCTID:403770008","NANDO:1200462","UMLS:C1275081","NORD:891","DOID:0060233","GARD:9146","NANDO:2200967","NCIT:C84617","OMIMPS:115150"],"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:0060581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of cells to specific cell fates and their capacity to differentiate into particular kinds of cells within a field of cells that will exhibit a certain pattern of differentiation. Positional information is established through protein signals that emanate from a localized source within a developmental field resulting in specification of a cell type. Those signals are then interpreted in a cell-autonomous manner resulting in the determination of the cell type.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate commitment","termid":"GO:0045165"},{"relation_name":"part_of","term_name":"pattern specification process","termid":"GO:0007389"}],"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 fate commitment involved in pattern specification","termid":"GO:0060581"}


id: FYPO:0007089
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 normally at the mitotic G2/M phase transition when the cell is subject to sulfur starvation.","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normally arrested mitotic cell cycle progression","termid":"FYPO:0001025"},{"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal cell cycle arrest at mitotic G2/M phase transition during sulfur starvation","synonyms":[{"name":"normal cell cycle arrest at mitotic G2/M phase transition during sulfur depletion","type":"exact"},{"name":"normal cell cycle arrest at mitotic G2/M phase transition during sulfur deprivation","type":"exact"},{"name":"normal cell cycle arrest at mitotic G2/M phase transition during sulfur limitation","type":"exact"},{"name":"normal cell cycle arrest in mitotic G2 phase during sulfur starvation","type":"related"},{"name":"normal mitotic cell cycle arrest at mitotic G2/M phase transition during sulfur starvation","type":"exact"}],"termid":"FYPO:0007089"}


id: FYECO:0000434
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed on normal medium after a short incubation in medium containing hydroxyurea.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transient hydroxyurea treatment","secondary_identifiers":["PMID:37200372"],"synonyms":[{"name":"acute hydroxyurea treatment","type":"broad"}],"termid":"FYECO:0000434"}


id: MONDO:0014163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any left ventricular noncompaction in which the cause of the disease is a mutation in the MYBPC3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"left ventricular noncompaction","termid":"MONDO:0018901"},{"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":"left ventricular noncompaction 10","secondary_identifiers":["MEDGEN:811617","UMLS:C3715165","OMIM:615396","GARD:15956"],"synonyms":[{"name":"LVNC10","type":"related"},{"name":"MYBPC3 left ventricular noncompaction","type":"exact"},{"name":"cardiomyopathy, dilated, 1Mm","type":"related"},{"name":"left ventricular noncompaction 10","type":"exact"},{"name":"left ventricular noncompaction caused by mutation in MYBPC3","type":"exact"},{"name":"left ventricular noncompaction type 10","type":"exact"}],"termid":"MONDO:0014163","xrefs":{"Monarch":{"xref_id":"0014163"}}}


id: MONDO:0018671
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"},{"relation_name":"is_a","term_name":"immunoglobulin G4-related sclerosing disease","termid":"MONDO:0017287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0005046"],"is_obsolete":false,"name":"IgG4-related kidney disease","secondary_identifiers":["UMLS:C5392056","GARD:21882","MEDGEN:1708840","Orphanet:449395","NANDO:1200930","icd11.foundation:1877692678"],"termid":"MONDO:0018671","xrefs":{"Monarch":{"xref_id":"0018671"}}}


id: PBO:0068458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 34, pseudogene","termid":"PBO:0068458"}


id: PR:O42869
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spa2 gene.","definition_xrefs":["UniProtKB:O42869","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 C3G9.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3G9.05","synonyms":[{"name":"Spom972h-spa2","type":"exact"}],"termid":"PR:O42869"}


id: _global:trans_spliced_from
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trans_spliced_from","termid":"_global:trans_spliced_from"}


id: GO:0042724
data:
  {"annotated_genes":["SJAG_00827","SJAG_04067","SJAG_02421","SJAG_03538","SJAG_04282","SJAG_03362","SJAG_02420","SJAG_02406","SJAG_04866","SJAG_00381","SJAG_01970"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90915,115695],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090180"},{"annotations":[62152,78791,71820,80239,75756,75698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009228"},{"annotations":[115607,79996,66817,115601,118042,68862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009229"},{"annotations":[112442,112441,101456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036172"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of thiamine (vitamin B1), and related compounds.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"water-soluble vitamin biosynthetic process","termid":"GO:0042364"},{"relation_name":"is_a","term_name":"thiamine-containing compound metabolic process","termid":"GO:0042723"},{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"},{"relation_name":"is_a","term_name":"pyrimidine-containing compound biosynthetic process","termid":"GO:0072528"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00381":null,"SJAG_00827":null,"SJAG_01970":null,"SJAG_02406":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_03362":null,"SJAG_03538":null,"SJAG_04067":null,"SJAG_04282":null,"SJAG_04866":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0006766","GO:0006790","GO:0008150"],"is_obsolete":false,"name":"thiamine-containing compound biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"thiamin and derivative biosynthesis","type":"exact"},{"name":"thiamin and derivative biosynthetic process","type":"exact"},{"name":"thiamin-containing compound biosynthetic process","type":"exact"},{"name":"thiamine and derivative biosynthesis","type":"exact"},{"name":"thiamine and derivative biosynthetic process","type":"exact"},{"name":"thiamine-containing compound anabolism","type":"exact"},{"name":"thiamine-containing compound biosynthesis","type":"exact"},{"name":"thiamine-containing compound formation","type":"exact"},{"name":"thiamine-containing compound synthesis","type":"exact"},{"name":"vitamin B1 and derivative biosynthesis","type":"exact"},{"name":"vitamin B1 and derivative biosynthetic process","type":"exact"}],"termid":"GO:0042724","terms_by_termid":{"GO:0009228":null,"GO:0009229":null,"GO:0036172":null,"GO:0090180":null}}


id: PATO:0001093
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001093 relative flux value (obsolete PATO:0001093)","termid":"PATO:0001093"}


id: PBO:0085254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peripheral membrane protein of the plasma membrane; interacts with Mid2p; regulates the cell integrity pathway mediated by Pkc1p and Slt2p; the authentic protein is detected in a phosphorylated state in highly purified mitochondria","termid":"PBO:0085254"}


id: PBO:0050809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HUNK antisense RNA 1","termid":"PBO:0050809"}


id: GO:0009152
data:
  {"annotated_genes":["SJAG_02038","SJAG_01859","SJAG_02598","SJAG_04123","SJAG_04849","SJAG_02887","SJAG_03925","SJAG_01298","SJAG_05204","SJAG_01081","SJAG_00985","SJAG_01661","SJAG_02364","SJAG_MIT15","SJAG_00836","SJAG_04634","SJAG_01814","SJAG_03140","SJAG_02564","SJAG_00915","SJAG_06634","SJAG_00438","SJAG_03114","SJAG_02850","SJAG_04681","SJAG_00964","SJAG_02105","SJAG_00044","SJAG_MIT37","SJAG_04122","SJAG_04422","SJAG_MIT09","SJAG_07003","SJAG_01070","SJAG_03355","SJAG_00542","SJAG_00133"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80750,78764],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044208"},{"annotations":[66780,65405,60495,58263,57122,73353,71677,78539],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006189"},{"annotations":[73662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006172"},{"annotations":[57274,75706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044209"},{"annotations":[63868,59782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006177"},{"annotations":[103136,77416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"},{"annotations":[104183,76675,65611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006183"},{"annotations":[65924,77417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032264"},{"annotations":[120038],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905707"},{"annotations":[95173,95764,109785,121124,106977,96754,105627,103763,109877,91007,94746,121118,117867,110775,104984,105601,121112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042776"},{"annotations":[77418,110254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a purine ribonucleotide, a compound consisting of ribonucleoside (a purine base linked to a ribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide biosynthetic process","termid":"GO:0006164"},{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"ribonucleotide biosynthetic process","termid":"GO:0009260"}],"gene_count":37,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00133":null,"SJAG_00438":null,"SJAG_00542":null,"SJAG_00836":null,"SJAG_00915":null,"SJAG_00964":null,"SJAG_00985":null,"SJAG_01070":null,"SJAG_01081":null,"SJAG_01298":null,"SJAG_01661":null,"SJAG_01814":null,"SJAG_01859":null,"SJAG_02038":null,"SJAG_02105":null,"SJAG_02364":null,"SJAG_02564":null,"SJAG_02598":null,"SJAG_02850":null,"SJAG_02887":null,"SJAG_03114":null,"SJAG_03140":null,"SJAG_03355":null,"SJAG_03925":null,"SJAG_04122":null,"SJAG_04123":null,"SJAG_04422":null,"SJAG_04634":null,"SJAG_04681":null,"SJAG_04849":null,"SJAG_05204":null,"SJAG_06634":null,"SJAG_07003":null,"SJAG_MIT09":null,"SJAG_MIT15":null,"SJAG_MIT37":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"purine ribonucleotide biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"purine ribonucleotide anabolism","type":"exact"},{"name":"purine ribonucleotide biosynthesis","type":"exact"},{"name":"purine ribonucleotide formation","type":"exact"},{"name":"purine ribonucleotide synthesis","type":"exact"}],"termid":"GO:0009152","terms_by_termid":{"GO:0006172":null,"GO:0006177":null,"GO:0006183":null,"GO:0006189":null,"GO:0032263":null,"GO:0032264":null,"GO:0032265":null,"GO:0042776":null,"GO:0044208":null,"GO:0044209":null,"GO:1905707":null}}


id: PBO:0077044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid hormone receptor alpha","termid":"PBO:0077044"}


id: GO:0050260
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribose 5-phosphate + ATP + NH4 = 5-phospho-D-ribosylamine + ADP + 2 H+ + phosphate.","definition_xrefs":["RHEA:13777","EC:6.3.4.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"ribose-5-phosphate-ammonia ligase activity","secondary_identifiers":["MetaCyc:RIBOSE-5-PHOSPHATE--AMMONIA-LIGASE-RXN","KEGG_REACTION:R01053"],"synonyms":[{"name":"5-phosphoribosylamine synthetase activity","type":"related"},{"name":"ammonia-ribose 5-phosphate aminotransferase activity","type":"related"},{"name":"ribose 5-phosphate aminotransferase activity","type":"related"},{"name":"ribose-5-phosphate:ammonia ligase (ADP-forming)","type":"related"}],"termid":"GO:0050260"}


id: GO:0002910
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of peripheral B cell deletion.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of peripheral tolerance induction","termid":"GO:0002660"},{"relation_name":"is_a","term_name":"positive regulation of B cell mediated immunity","termid":"GO:0002714"},{"relation_name":"is_a","term_name":"positive regulation of B cell deletion","termid":"GO:0002869"},{"relation_name":"is_a","term_name":"regulation of peripheral B cell deletion","termid":"GO:0002908"},{"relation_name":"positively_regulates","term_name":"peripheral B cell deletion","termid":"GO:0002454"}],"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 peripheral B cell deletion","synonyms":[{"name":"activation of peripheral B cell deletion","type":"narrow"},{"name":"stimulation of peripheral B cell deletion","type":"narrow"},{"name":"up regulation of peripheral B cell deletion","type":"exact"},{"name":"up-regulation of peripheral B cell deletion","type":"exact"},{"name":"upregulation of peripheral B cell deletion","type":"exact"}],"termid":"GO:0002910"}


id: MONDO:0002056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign tumor of the breast characterized by the presence of stromal and epithelial elements. It presents as a painless, solitary, slow growing, firm, and mobile mass. It is the most common benign breast lesion. It usually occurs in women of childbearing age. The majority of fibroadenomas do not recur after complete excision. A slightly increased risk of developing cancer within fibroadenomas or in the breast tissue of patients previously treated for fibroadenomas has been reported.","definition_xrefs":["NCIT:C3744"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"breast fibroepithelial neoplasm","termid":"MONDO:0021046"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast fibroadenoma","secondary_identifiers":["ONCOTREE:FA","SCTID:254847007","UMLS:C0178421","ICDO:9010/0","MEDGEN:64231","DOID:1618","MESH:D018226"],"synonyms":[{"name":"Complex fibroadenoma of breast","type":"exact"},{"name":"FA","type":"related"},{"name":"breast fibroadenoma","type":"exact"},{"name":"cellular fibroadenoma","type":"exact"},{"name":"fibroadenoma","type":"exact"},{"name":"fibroadenoma of breast","type":"exact"},{"name":"fibroadenoma of the breast","type":"exact"},{"name":"fibroadenoma, benign","type":"exact"},{"name":"juvenile fibroadenoma","type":"exact"},{"name":"juvenile fibroadenoma (morphologic abnormality)","type":"exact"},{"name":"juvenile fibroadenoma of breast","type":"exact"}],"termid":"MONDO:0002056","xrefs":{"Monarch":{"xref_id":"0002056"}}}


id: PBO:0081634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 562","termid":"PBO:0081634"}


id: PBO:0042723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENPB DNA-binding domain containing 1, pseudogene","termid":"PBO:0042723"}


id: PATO:0001090
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001090 absolute elasticity value (obsolete PATO:0001090)","termid":"PATO:0001090"}


id: GO:0102586
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cyanidin 3-O-[2''-O-(xylosyl)-6''-O-(p-coumaroyl) glucoside] 5-O-malonylglucoside + 1-O-sinapoyl-beta-D-glucose = cyanidin 3-O-[2''-O-(2''-O-(sinapoyl) xylosyl) 6'-O-(p-coumaroyl) glucoside] 5-O-[6''-O-(malonyl) glucoside + beta-D-glucose.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete cyanidin 3-O-[2''-O-(2''-O-(sinapoyl) xylosyl) 6''-O-(p-coumaroyl) glucoside] 5-O-[6''-O-(malonyl) glucoside] sinapoyltransferase activity (obsolete GO:0102586)","termid":"GO:0102586"}


id: GO:0044181
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a multicellular organism grows in a threadlike, filamentous shape.","definition_xrefs":["GOC:mtg_cambridge_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"filamentous growth","termid":"GO:0030447"},{"relation_name":"is_a","term_name":"developmental growth involved in morphogenesis","termid":"GO:0060560"}],"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":"filamentous growth of a multicellular organism","termid":"GO:0044181"}


id: PR:O42976
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC20F10.07 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42976"],"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 membrane protein C20F10.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC20F10.07","synonyms":[{"name":"Spom972h-SPBC20F10.07","type":"exact"}],"termid":"PR:O42976"}


id: PBO:0047832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box P3","termid":"PBO:0047832"}


id: GO:0033059
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The deposition or aggregation of coloring matter in a cell.","definition_xrefs":["GOC:mtg_MIT_16mar07"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"},{"relation_name":"is_a","term_name":"pigmentation","termid":"GO:0043473"}],"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 pigmentation","termid":"GO:0033059"}


id: GO:0103023
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ITP + H2O = IDP + H+ + phosphate.","definition_xrefs":["PMID:16216582","RHEA:28330","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoside triphosphate phosphatase activity","termid":"GO:0017111"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"ITPase activity","secondary_identifiers":["EC:3.6.1.73","MetaCyc:RXN0-5073"],"termid":"GO:0103023"}


id: PBO:0036395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human MAPK organizer 1 (MORG1) family Wdr83 (predicted)","termid":"PBO:0036395"}


id: PATO:0000015
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A chromatic scalar-circular quality inhering in an object that manifests in an observer by virtue of the dominant wavelength of the visible light; may be subject to fiat divisions, typically into 7 or 8 spectra.","definition_xrefs":["PATOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatic property","termid":"PATO:0001301"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"color hue","termid":"PATO:0000015"}


id: PATO:0000771
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A preference quality in a bearer by virtue of the bearer's disliking a perceived stimulus.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"preference","termid":"PATO:0000773"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aversion","termid":"PATO:0000771"}


id: GO:0030711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of border cell delamination.","definition_xrefs":["PMID:10822261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of border follicle cell delamination","termid":"GO:0030710"},{"relation_name":"is_a","term_name":"positive regulation of biological process","termid":"GO:0048518"},{"relation_name":"positively_regulates","term_name":"border follicle cell delamination","termid":"GO:0030709"}],"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":"positive regulation of border follicle cell delamination","synonyms":[{"name":"activation of border follicle cell delamination","type":"narrow"},{"name":"positive regulation of border cell delamination","type":"broad"},{"name":"stimulation of border follicle cell delamination","type":"narrow"},{"name":"up regulation of border follicle cell delamination","type":"exact"},{"name":"up-regulation of border follicle cell delamination","type":"exact"},{"name":"upregulation of border follicle cell delamination","type":"exact"}],"termid":"GO:0030711"}


id: PBO:0086529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved among S. cerevisiae strains","termid":"PBO:0086529"}


id: PBO:0083985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glutamine synthetase (GS); synthesizes glutamine from glutamate and ammonia; with Glt1p, forms the secondary pathway for glutamate biosynthesis from ammonia; expression regulated by nitrogen source and by amino acid limitation; forms filaments of back-to-back stacks of cylindrical homo-decamers at low pH, leading to enzymatic inactivation and storage during states of advanced cellular starvation; relocalizes from nucleus to cytoplasmic foci upon DNA replication stress","termid":"PBO:0083985"}


id: PBO:0045240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 8","termid":"PBO:0045240"}


id: PBO:0074309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMAD1 antisense RNA 2","termid":"PBO:0074309"}


id: FYPO:0004569
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the presence, distribution, or morphology of the meiotic spindle is normal (i.e. indistinguishable from wild type) during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal spindle","termid":"FYPO:0004568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal spindle during meiosis I","synonyms":[{"name":"normal meiosis I spindle","type":"exact"},{"name":"normal meiotic spindle during meiosis I","type":"exact"},{"name":"normal spindle during first meiotic nuclear division","type":"related"}],"termid":"FYPO:0004569"}


id: PBO:0072884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SET binding factor 2","termid":"PBO:0072884"}


id: PR:O94728
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1604.16c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94728"],"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 C1604.16c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.16c","synonyms":[{"name":"Spom972h-SPBC1604.16c","type":"exact"}],"termid":"PR:O94728"}


id: PBO:0002831
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protease S. Pombe","termid":"PBO:0002831"}


id: MONDO:1010147
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Stiff skin syndrome that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stiff skin syndrome, non-human animal","secondary_identifiers":["OMIA:002018"],"termid":"MONDO:1010147","xrefs":{"Monarch":{"xref_id":"1010147"}}}


id: MONDO:0014629
data:
  {"annotated_genes":["SJAG_04569"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89142],"is_not":false,"summary":null,"term":"MONDO:0014629"}]},"cv_name":"mondo","definition":"A respiratory disease characterized by interstitial lung disease (often with pulmonary hemorrhage) and inflammatory arthritis, associated with high-titer autoantibodies (including anti-nuclear and anti-neutrophil cytoplasmic antibodies, and rheumatoid factor). Patients present from infancy to adolescence with tachypnea, cough, hemoptysis, and/or joint pain. Some patients may also develop glomerular disease.","definition_xrefs":["Orphanet:444092"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary interstitial lung disease specific to childhood associated with a systemic disease (obsolete MONDO:0017020)","termid":"MONDO:0017020"},{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"type 1 interferonopathy of childhood","termid":"MONDO:0957408"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04569":null},"genotype_count":0,"is_obsolete":false,"name":"autoimmune interstitial lung disease-arthritis syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1800821","NORD:1973","OMIM:616414","DOID:0081242","GARD:17762","UMLS:C5243948"],"synonyms":[{"name":"AILJK","type":"related"},{"name":"COPA Syndrome","type":"exact"},{"name":"autoimmune interstitial lung, joint, and kidney disease","type":"related"},{"name":"copa defect","type":"exact"},{"name":"copa syndrome","type":"exact"}],"termid":"MONDO:0014629","terms_by_termid":{"MONDO:0014629":null},"xrefs":{"Monarch":{"xref_id":"0014629"}}}


id: PBO:0039202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldo-keto reductase family 1 member B1 pseudogene 5","termid":"PBO:0039202"}


id: GO:0007078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which lamin is depolymerized.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein depolymerization","termid":"GO:0051261"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic nuclear membrane disassembly","termid":"GO:0007077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"lamin depolymerization","termid":"GO:0007078"}


id: GO:0106005
data:
  {"annotated_genes":["SJAG_04034"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60386],"is_not":false,"summary":null,"term":"GO:0106005"}]},"cv_name":"biological_process","definition":"The process whereby a guanine in 5-cap is methylated at the N7 position of guanine.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA (guanine-N7)-methylation","termid":"GO:0036265"},{"relation_name":"part_of","term_name":"7-methylguanosine RNA capping","termid":"GO:0009452"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04034":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"RNA 5'-cap (guanine-N7)-methylation","references_by_uniquename":{"GO_REF:0000108":null},"termid":"GO:0106005","terms_by_termid":{"GO:0106005":null}}


id: MONDO:0004350
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinoblastoma during childhood that has spread beyond the eye.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extraocular retinoblastoma","termid":"MONDO:0003078"},{"relation_name":"is_a","term_name":"childhood malignant neoplasm","termid":"MONDO:0006517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004992"],"is_obsolete":false,"name":"pediatric extraocular retinoblastoma","secondary_identifiers":["MEDGEN:230837","UMLS:C1321870","NCIT:C9048","DOID:7747"],"synonyms":[{"name":"childhood extraocular retinoblastoma","type":"exact"},{"name":"childhood metastatic retinoblastoma","type":"exact"},{"name":"extraocular retinoblastoma","type":"broad"},{"name":"extraocular retinoblastoma of childhood","type":"exact"},{"name":"pediatric extraocular retinoblastoma","type":"exact"}],"termid":"MONDO:0004350","xrefs":{"Monarch":{"xref_id":"0004350"}}}


id: PBO:0090674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hrd1 ubiquitin ligase complex subunit Ufd1","termid":"PBO:0090674"}


id: PBO:0004519
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.5.4.12","termid":"PBO:0004519"}


id: GO:0140120
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H2A ubiquitinated at lysine 15.","definition_xrefs":["PMID:23760478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2A reader activity","termid":"GO:0140054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140566"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0060090","GO:0030674","GO:0140566","GO:0003674"],"is_obsolete":false,"name":"histone H2AK15ub reader activity","termid":"GO:0140120"}


id: PBO:0060246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYCBP2 antisense RNA 1","termid":"PBO:0060246"}


id: PBO:0030530
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_L-aminoadipate-semialdehyde_dehydrogenase_activity","termid":"PBO:0030530"}


id: GO:1900694
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of (+)-kotanin biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"is_a","term_name":"regulation of (+)-kotanin biosynthetic process","termid":"GO:1900692"},{"relation_name":"positively_regulates","term_name":"(+)-kotanin biosynthetic process","termid":"GO:1900596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"positive regulation of (+)-kotanin biosynthetic process","synonyms":[{"name":"activation of (+)-kotanin anabolism","type":"exact"},{"name":"activation of (+)-kotanin biosynthesis","type":"exact"},{"name":"activation of (+)-kotanin biosynthetic process","type":"narrow"},{"name":"activation of (+)-kotanin formation","type":"exact"},{"name":"activation of (+)-kotanin synthesis","type":"exact"},{"name":"positive regulation of (+)-kotanin anabolism","type":"exact"},{"name":"positive regulation of (+)-kotanin biosynthesis","type":"exact"},{"name":"positive regulation of (+)-kotanin formation","type":"exact"},{"name":"positive regulation of (+)-kotanin synthesis","type":"exact"},{"name":"up regulation of (+)-kotanin anabolism","type":"exact"},{"name":"up regulation of (+)-kotanin biosynthesis","type":"exact"},{"name":"up regulation of (+)-kotanin biosynthetic process","type":"exact"},{"name":"up regulation of (+)-kotanin formation","type":"exact"},{"name":"up regulation of (+)-kotanin synthesis","type":"exact"},{"name":"up-regulation of (+)-kotanin anabolism","type":"exact"},{"name":"up-regulation of (+)-kotanin biosynthesis","type":"exact"},{"name":"up-regulation of (+)-kotanin biosynthetic process","type":"exact"},{"name":"up-regulation of (+)-kotanin formation","type":"exact"},{"name":"up-regulation of (+)-kotanin synthesis","type":"exact"},{"name":"upregulation of (+)-kotanin anabolism","type":"exact"},{"name":"upregulation of (+)-kotanin biosynthesis","type":"exact"},{"name":"upregulation of (+)-kotanin biosynthetic process","type":"exact"},{"name":"upregulation of (+)-kotanin formation","type":"exact"},{"name":"upregulation of (+)-kotanin synthesis","type":"exact"}],"termid":"GO:1900694"}


id: MONDO:0009283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glutaryl-CoA oxidase deficiency is a peroxisomal disorder leading to glutaric aciduria. The prevalence is unknown. There is no distinctive phenotype associated with this disorder and one of the reported cases was asymptomatic. Transmission appears to be autosomal recessive.","definition_xrefs":["Orphanet:35706"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete disorder of peroxisomal alpha-, beta- and omega-oxidation (obsolete MONDO:0017753)","termid":"MONDO:0017753"},{"relation_name":"is_a","term_name":"glutaric aciduria","termid":"MONDO:0000129"},{"relation_name":"is_a","term_name":"inborn organic aciduria","termid":"MONDO:0000688"}],"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":"glutaric acidemia type 3","secondary_identifiers":["MESH:C562818","GARD:12469","MEDGEN:87464","ICD10CM:E72.3","ICD9:270.2","UMLS:C0342873","OMIM:231690","SCTID:238070003","DOID:0112246"],"synonyms":[{"name":"GA III","type":"related"},{"name":"GA3","type":"related"},{"name":"Ga 3","type":"related"},{"name":"SUGCT glutaric aciduria (disease)","type":"exact"},{"name":"glutaric acidemia type 3","type":"exact"},{"name":"glutaric acidemia type III","type":"related"},{"name":"glutaric aciduria (disease) caused by mutation in SUGCT","type":"exact"},{"name":"glutaric aciduria 3","type":"related"},{"name":"glutaric aciduria III","type":"related"},{"name":"glutaric aciduria type 3","type":"exact"},{"name":"glutaric aciduria type III","type":"related"},{"name":"glutaryl-CoA oxidase deficiency","type":"exact"},{"name":"glutaryl-Coa oxidase deficiency","type":"related"}],"termid":"MONDO:0009283","xrefs":{"Monarch":{"xref_id":"0009283"}}}


id: GO:0001722
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Low molecular weight (10-45 kDa) proteins that associate with intermediate filaments by lateral binding of the filaments and have the effect of creating tight macrofilament aggregates.","definition_xrefs":["GOC:ajp","PMID:9484600"],"gene_count":0,"genotype_count":0,"name":"obsolete type I intermediate filament associated protein (obsolete GO:0001722)","synonyms":[{"name":"type I intermediate filament associated protein","type":"exact"}],"termid":"GO:0001722"}


id: PBO:0078814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trophinin","termid":"PBO:0078814"}


id: PBO:0002728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-HIT protein Hit1 (predicted)","termid":"PBO:0002728"}


id: PBO:0087010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribonuclease H2 catalytic subunit; removes RNA primers during Okazaki fragment synthesis and errant ribonucleotides misincorporated during DNA replication; role in ribonucleotide excision repair; homolog of RNAse HI; related to human AGS4 which causes Aicardi-Goutieres syndrome","termid":"PBO:0087010"}


id: PBO:0090627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SDA1 family protein","termid":"PBO:0090627"}


id: GO:0097664
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An SCF ubiquitin ligase complex in which the F-box protein is Grr1 in S. cerevisiae (Pof2 in S. pombe).","definition_xrefs":["PMID:10213692","PMID:15147268","GOC:jd","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SCF ubiquitin ligase complex","termid":"GO:0019005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"SCF-Grr1/Pof2 ubiquitin ligase complex","termid":"GO:0097664"}


id: MONDO:0005719
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Virus diseases caused by the coronavirus genus. Some specifics include transmissible enteritis of turkeys (enteritis, transmissible, of turkeys); feline infectious peritonitis; and transmissible gastroenteritis of swine (gastroenteritis, transmissible, of swine).","definition_xrefs":["MESH:D018352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Coronaviridae infectious disease","termid":"MONDO:0005718"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Coronavinae infectious disease","secondary_identifiers":["EFO:0007224"],"termid":"MONDO:0005719","xrefs":{"Monarch":{"xref_id":"0005719"}}}


id: GO:0009317
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that catalyzes the first step in long-chain fatty acid biosynthesis. For example, in E. coli the complex is heterohexameric and composed of biotin carbonyl carrier protein, biotin carboxylase and the acetate CoA-transferase complex.","definition_xrefs":["PMID:12121720","GOC:mah","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"acetyl-CoA carboxylase complex","synonyms":[{"name":"ACCase complex","type":"exact"}],"termid":"GO:0009317"}


id: PBO:0076591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 12","termid":"PBO:0076591"}


id: GO:0045961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the consistent predetermined time point at which an integrated living unit or organism progresses from an initial condition to a later condition and decreases the rate at which this time point is reached.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of development, heterochronic","termid":"GO:0040034"}],"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 development, heterochronic","synonyms":[{"name":"down regulation of development, heterochronic","type":"exact"},{"name":"down-regulation of development, heterochronic","type":"exact"},{"name":"downregulation of development, heterochronic","type":"exact"},{"name":"inhibition of development, heterochronic","type":"narrow"}],"termid":"GO:0045961"}


id: PBO:0042120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 192","termid":"PBO:0042120"}


id: PBO:0108907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1191 pseudogene 1","termid":"PBO:0108907"}


id: GO:0102742
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + 3,4-dihydroxyphenylpyruvate + NADPH = (2R)-3-(3,4-dihydroxyphenyl)lactate + NADP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete R(+)-3,4-dihydroxyphenyllactate:NADP+ oxidoreductase activity (obsolete GO:0102742)","termid":"GO:0102742"}


id: PBO:0001250
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAtabolism of Arginine, after cerevisiae","termid":"PBO:0001250"}


id: PBO:0028987
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_sporulation_resulting_in_formation_of_ascus_with_more_than_four_spores","termid":"PBO:0028987"}


id: MONDO:0019044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tumor of hematopoietic and lymphoid tissues (obsolete MONDO:0019044)","secondary_identifiers":["Orphanet:68347"],"termid":"MONDO:0019044","xrefs":{"Monarch":{"xref_id":"0019044"}}}


id: PBO:0063853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol binding clathrin assembly protein","termid":"PBO:0063853"}


id: GO:0010855
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and decreases the activity of adenylate cyclase.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclase inhibitor activity","termid":"GO:0010852"},{"relation_name":"is_a","term_name":"adenylate cyclase regulator activity","termid":"GO:0010854"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0004857","GO:0030234","GO:0098772","GO:0003674","GO:0140678"],"is_obsolete":false,"name":"adenylate cyclase inhibitor activity","secondary_identifiers":["Reactome:R-HSA-400097"],"termid":"GO:0010855"}


id: MONDO:0022573
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"biliary atresia","termid":"MONDO:0008867"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"biliary atresia intrahepatic non syndromic form","secondary_identifiers":["GARD:887"],"termid":"MONDO:0022573","xrefs":{"Monarch":{"xref_id":"0022573"}}}


id: MONDO:0003614
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign neoplasm characterized by the presence of smooth muscle cells growing within veins.","definition_xrefs":["NCIT:C4518"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyomatosis","termid":"MONDO:0003295"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intravenous leiomyomatosis","secondary_identifiers":["DOID:5729","ICD9:238.1","MEDGEN:83417","UMLS:C0346200","SCTID:254883003"],"synonyms":[{"name":"intravenous leiomyomatosis","type":"exact"}],"termid":"MONDO:0003614","xrefs":{"Monarch":{"xref_id":"0003614"}}}


id: MONDO:0006921
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with bacteria of the order actinomycetales.","definition_xrefs":["MESH:D000193"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gram-positive bacterial infections","termid":"MONDO:0021679"},{"relation_name":"is_a","term_name":"anaerobic bacteria infectious disease","termid":"MONDO:0024389"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Actinomycetales infectious disease","secondary_identifiers":["SCTID:11817007","EFO:1001122","UMLS:C0001255","ICD9:039.8","SCTID:721751007","MEDGEN:1732","ICD9:039.9","NCIT:C84534"],"synonyms":[{"name":"actinomycetales caused disease or disorder","type":"exact"},{"name":"actinomycetales disease or disorder","type":"exact"},{"name":"actinomycetales infection","type":"exact"},{"name":"actinomycetales infections","type":"exact"},{"name":"actinomycete infection","type":"exact"},{"name":"actinomycete infections","type":"exact"},{"name":"actinomycosis","type":"related"},{"name":"actinomycotic infection","type":"exact"},{"name":"actinomycotic infectious disease","type":"exact"},{"name":"infection caused by actinomycetales","type":"related"},{"name":"infection, actinomycetales","type":"exact"},{"name":"infection, actinomycete","type":"exact"},{"name":"infections, actinomycetales","type":"exact"},{"name":"infections, actinomycete","type":"exact"}],"termid":"MONDO:0006921","xrefs":{"Monarch":{"xref_id":"0006921"}}}


id: PBO:0047475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"farnesyl diphosphate synthase pseudogene 2","termid":"PBO:0047475"}


id: PBO:0064463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase delta 1, catalytic subunit","termid":"PBO:0064463"}


id: MONDO:0016239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cystinosis is a metabolic disease characterized by an accumulation of cystine inside the lysosomes, causing damage in different organs and tissues, particularly in the kidneys and eyes. Three clinical forms have been described: nephropathic infantile, nephropathic juvenile and ocular.","definition_xrefs":["Orphanet:213"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of lysosomal amino acid transport","termid":"MONDO:0019246"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0005066"],"is_obsolete":false,"name":"cystinosis","secondary_identifiers":["NORD:1028","SCTID:190681003","UMLS:C4316899","MESH:D003554","DOID:1064","ICD10CM:E72.04","GARD:6236","NANDO:2200571","NANDO:1200161","icd11.foundation:733715856","MedDRA:10011777","NCIT:C2976","MEDGEN:1384792"],"synonyms":[{"name":"Cystinoses","type":"related"},{"name":"Protein defect of cystin transport","type":"exact"},{"name":"cystine diathesis","type":"related"},{"name":"cystine disease","type":"related"},{"name":"cystine storage disease","type":"exact"},{"name":"cystinosis","type":"exact"}],"termid":"MONDO:0016239","xrefs":{"Monarch":{"xref_id":"0016239"}}}


id: GO:0050476
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + acetylenedicarboxylate = CO2 + pyruvate.","definition_xrefs":["EC:4.1.1.78"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"acetylenedicarboxylate decarboxylase activity","secondary_identifiers":["MetaCyc:4.1.1.78-RXN","RHEA:17733"],"synonyms":[{"name":"acetylenedicarboxylate carboxy-lyase (pyruvate-forming)","type":"related"},{"name":"acetylenedicarboxylate carboxy-lyase activity","type":"related"},{"name":"acetylenedicarboxylate hydrase activity","type":"related"},{"name":"acetylenedicarboxylate hydratase activity","type":"related"}],"termid":"GO:0050476"}


id: PBO:0055703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LLPH pseudogene 2","termid":"PBO:0055703"}


id: PBO:0049522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A.P histone","termid":"PBO:0049522"}


id: FYPO:0005771
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone H2A phosphorylation occurs to a greater extent than normal in regions where nucleosomes are depleted. All histone H2A phosphorylation may be affected, or phosphorylation of specific sites on histone H2A may be increased.","definition_xrefs":["PMID:27611590","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H2A phosphorylation during vegetative growth","termid":"FYPO:0002596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0002274","FYPO:0001985","FYPO:0000002","FYPO:0002494"],"is_obsolete":false,"name":"increased histone H2A phosphorylation at nucleosome-depleted regions during vegetative growth","synonyms":[{"name":"increased histone H2A phosphorylation at nucleosome-depleted regions during mitotic cell cycle","type":"related"}],"termid":"FYPO:0005771"}


id: PBO:0045211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C5 beta","termid":"PBO:0045211"}


id: GO:0038120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of the C-C chemokine CCL21 to a C-C chemokine type 7 receptor (CCR7) on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:15059845","GOC:nhn","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine (C-C motif) ligand 21 signaling pathway","termid":"GO:0038116"},{"relation_name":"is_a","term_name":"C-C chemokine receptor CCR7 signaling pathway","termid":"GO:0038118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"CCL21-activated CCR7 signaling pathway","synonyms":[{"name":"CCL21-activated CCR7 signalling pathway","type":"exact"}],"termid":"GO:0038120"}


id: PR:P79009
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps2502 gene.","definition_xrefs":["UniProtKB:P79009","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 S25-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC694.05c","synonyms":[{"name":"S31-A (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rps2502","type":"exact"}],"termid":"PR:P79009"}


id: MONDO:0011108
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Stüve-Wiedemann syndrome (obsolete MONDO:0011108)","termid":"MONDO:0011108","xrefs":{"Monarch":{"xref_id":"0011108"}}}


id: PBO:0091077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall and secondary septum 1,6 branched 1,3-beta-glucan synthase catalytic subunit Bgs4","termid":"PBO:0091077"}


id: GO:1900722
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein adenylylation.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification process","termid":"GO:0031399"},{"relation_name":"regulates","term_name":"protein adenylylation","termid":"GO:0018117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of protein adenylylation","synonyms":[{"name":"regulation of protein AMPylation","type":"exact"},{"name":"regulation of protein adenylation","type":"exact"},{"name":"regulation of protein amino acid adenylylation","type":"exact"}],"termid":"GO:1900722"}


id: MONDO:1012118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypoplasia of mammary gland, non-human animal","termid":"MONDO:1011677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital hypoplasia of mammary gland, sheep","secondary_identifiers":["OMIA:000529-9940"],"termid":"MONDO:1012118","xrefs":{"Monarch":{"xref_id":"1012118"}}}


id: GO:0034923
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: phenanthrene-4,5-dicarboxylate + H+ = phenanthrene-4-carboxylate + CO2.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete phenanthrene-4,5-dicarboxylate decarboxylase activity (obsolete GO:0034923)","termid":"GO:0034923"}


id: GO:0030604
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-C-methyl-D-erythritol 4-phosphate + NADP+ = 1-deoxy-D-xylulose 5-phosphate + H+ + NADPH.","definition_xrefs":["EC:1.1.1.267","RHEA:13717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"1-deoxy-D-xylulose-5-phosphate reductoisomerase activity","secondary_identifiers":["KEGG_REACTION:R05688","MetaCyc:DXPREDISOM-RXN"],"synonyms":[{"name":"1-deoxy-D-xylulose-5-phosphate isomeroreductase activity","type":"related"},{"name":"1-deoxyxylulose-5-phosphate reductoisomerase activity","type":"related"},{"name":"2-C-methyl-D-erythritol-4-phosphate:NADP+ oxidoreductase (isomerizing)","type":"related"},{"name":"2C-methyl-D-erythritol-4-phosphate (MEP) synthase activity","type":"related"},{"name":"DOXP reductoisomerase activity","type":"exact"},{"name":"DXP-reductoisomerase activity","type":"related"}],"termid":"GO:0030604"}


id: PBO:0004030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial outer membrane translocase complex Tom5 (predicted)","termid":"PBO:0004030"}


id: PBO:0038547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABHD17A pseudogene 1","termid":"PBO:0038547"}


id: GO:0042402
data:
  {"annotated_genes":["SJAG_03288"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009447"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways occurring at the level of individual cells resulting in the breakdown of biogenic amines, any of a group of naturally occurring, biologically active amines, such as norepinephrine, histamine, and serotonin, many of which act as neurotransmitters.","definition_xrefs":["ISBN:0198506732","GOC:go_curators","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amine catabolic process","termid":"GO:0009310"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03288":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"biogenic amine catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"biogenic amine breakdown","type":"exact"},{"name":"biogenic amine catabolism","type":"exact"},{"name":"biogenic amine degradation","type":"exact"}],"termid":"GO:0042402","terms_by_termid":{"GO:0009447":null}}


id: GO:0016262
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-glucosamine + protein = UDP + 4-N-(N-acetyl-D-glucosaminyl)-protein.","definition_xrefs":["EC:2.4.1.94"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0140096","GO:0016757","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"protein N-acetylglucosaminyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.94-RXN","RHEA:16533","GO:0016253"],"synonyms":[{"name":"N-GlcNAc transferase activity","type":"related"},{"name":"UDP-N-acetyl-D-glucosamine:protein beta-N-acetyl-D-glucosaminyl-transferase activity","type":"exact"},{"name":"UDP-N-acetylglucosamine-peptide N-acetylglucosaminyltransferase activity","type":"exact"},{"name":"protein N-GlcNAc transferase activity","type":"exact"},{"name":"uridine diphospho-N-acetylglucosamine:polypeptide beta-N-acetylglucosaminyltransferase activity","type":"exact"},{"name":"uridine diphosphoacetylglucosamine-protein acetylglucosaminyltransferase activity","type":"exact"}],"termid":"GO:0016262"}


id: MONDO:1011745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"comedo syndrome, non-human animal","secondary_identifiers":["OMIA:001272"],"termid":"MONDO:1011745","xrefs":{"Monarch":{"xref_id":"1011745"}}}


id: PBO:0042174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cellular communication network factor 4","termid":"PBO:0042174"}


id: PBO:0085488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Proliferating cell nuclear antigen (PCNA); functions as the sliding replication clamp for DNA polymerase delta; may function as a docking site for other proteins required for mitotic and meiotic chromosomal DNA replication and for DNA repair; PCNA ubiquitination at K164 plays a crucial role during Okazaki fragment processing","termid":"PBO:0085488"}


id: GO:1901063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of guaiacyl lignin.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignin biosynthetic process","termid":"GO:0009809"},{"relation_name":"is_a","term_name":"guaiacyl lignin metabolic process","termid":"GO:1901061"}],"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":"guaiacyl lignin biosynthetic process","synonyms":[{"name":"G-lignin biosynthetic process","type":"exact"},{"name":"guaiacyl lignin anabolism","type":"exact"},{"name":"guaiacyl lignin biosynthesis","type":"exact"},{"name":"guaiacyl lignin formation","type":"exact"},{"name":"guaiacyl lignin synthesis","type":"exact"}],"termid":"GO:1901063"}


id: GO:0050205
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: carbamoyl phosphate + oxamate = oxalurate + phosphate.","definition_xrefs":["EC:2.1.3.5","RHEA:22984"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxyl- or carbamoyltransferase activity","termid":"GO:0016743"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"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:0016741","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"oxamate carbamoyltransferase activity","secondary_identifiers":["MetaCyc:OXAMATE-CARBAMOYLTRANSFERASE-RXN","KEGG_REACTION:R02937"],"synonyms":[{"name":"carbamoyl-phosphate:oxamate carbamoyltransferase activity","type":"related"},{"name":"oxamic transcarbamylase activity","type":"related"}],"termid":"GO:0050205"}


id: PBO:0086690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; induced by cell wall perturbation","termid":"PBO:0086690"}


id: MONDO:0017816
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary systemic amyloidosis (PSA) is a form of AL amyloidosis caused by the aggregation and deposition of insoluble amyloid fibrils derived from misfolded monoclonal immunoglobulin light chains usually produced by a plasma cell tumor and characterized by multiple organ involvement.","definition_xrefs":["Orphanet:314701"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AL amyloidosis","termid":"MONDO:0019438"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"primary systemic amyloidosis","secondary_identifiers":["SCTID:89449005","MEDGEN:129028","NCIT:C8299","UMLS:C0281479","NANDO:1200209","GARD:17431"],"synonyms":[{"name":"systemic AL amyloidosis","type":"exact"},{"name":"systemic Immunoglobulin Light chain amyloidosis","type":"exact"},{"name":"systemic amyloidosis","type":"exact"}],"termid":"MONDO:0017816","xrefs":{"Monarch":{"xref_id":"0017816"}}}


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


id: PBO:0080594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 24","termid":"PBO:0080594"}


id: PR:Q9HGP1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC29B5.04c gene.","definition_xrefs":["UniProtKB:Q9HGP1","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 C29B5.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29B5.04c","synonyms":[{"name":"Spom972h-SPBC29B5.04c","type":"exact"}],"termid":"PR:Q9HGP1"}


id: FYPO:0003648
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which a cell population does not grow in a medium containing xanthine as the nitrogen source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished vegetative cell population growth","termid":"FYPO:0001575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985","FYPO:0005447","FYPO:0000139","FYPO:0002060","FYPO:0002058","FYPO:0002057"],"is_obsolete":false,"name":"abolished cell population growth on xanthine nitrogen source","synonyms":[{"name":"abolished growth on xanthine nitrogen source","type":"broad"},{"name":"abolished vegetative cell population growth on xanthine nitrogen source","type":"exact"},{"name":"abolished xanthine utilization","type":"related"},{"name":"cell population growth on xanthine nitrogen source abolished","type":"exact"}],"termid":"FYPO:0003648"}


id: PBO:0075867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family pseudogene 7","termid":"PBO:0075867"}


id: GO:0004230
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the release of a N-terminal glutamate (and to a lesser extent aspartate) from a peptide.","definition_xrefs":["EC:3.4.11.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminopeptidase activity","termid":"GO:0004177"}],"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:0008233"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0008233","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"glutamyl aminopeptidase activity","secondary_identifiers":["MetaCyc:3.4.11.7-RXN"],"synonyms":[{"name":"Ca2+-activated glutamate aminopeptidase activity","type":"related"},{"name":"L-aspartate aminopeptidase activity","type":"related"},{"name":"aminopeptidase A","type":"related"},{"name":"angiotensinase A","type":"related"},{"name":"angiotensinase A2","type":"related"},{"name":"antigen BP-1/6C3 of mouse B lymphocytes","type":"related"},{"name":"aspartate aminopeptidase activity","type":"related"},{"name":"glutamyl peptidase activity","type":"related"},{"name":"membrane aminopeptidase II","type":"related"}],"termid":"GO:0004230"}


id: GO:0051658
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which the nucleus is maintained in a specific location within a cell and prevented from moving elsewhere.","definition_xrefs":["GOC:dph","GOC:ai","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus localization","termid":"GO:0051647"},{"relation_name":"is_a","term_name":"maintenance of organelle location","termid":"GO:0051657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"maintenance of nucleus location","synonyms":[{"name":"maintenance of cell nucleus location","type":"exact"},{"name":"maintenance of nucleus localization","type":"related"}],"termid":"GO:0051658"}


id: PR:Q09744
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC12C2.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09744"],"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 FAD-binding protein C12C2.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12C2.03c","synonyms":[{"name":"Spom972h-SPBC12C2.03c","type":"exact"}],"termid":"PR:Q09744"}


id: PBO:0087313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Small subunit of the clathrin-associated adaptor complex AP-1; AP-1 is involved in protein sorting at the trans-Golgi network; homolog of the sigma subunit of the mammalian clathrin AP-1 complex","termid":"PBO:0087313"}


id: MONDO:1012091
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"gastric dilatation volvulus syndrome, non-human animal","termid":"MONDO:1011659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gastric dilatation volvulus syndrome, dog","secondary_identifiers":["OMIA:000404-9615"],"termid":"MONDO:1012091","xrefs":{"Monarch":{"xref_id":"1012091"}}}


id: GO:0043534
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of an endothelial cell into the extracellular matrix in order to form new blood vessels during angiogenesis.","definition_xrefs":["PMID:11166264"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell migration","termid":"GO:0043542"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"blood vessel endothelial cell migration","termid":"GO:0043534"}


id: GO:0051040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the attachment of one cell to another cell via adhesion molecules that do not require the presence of calcium for the interaction.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell-cell adhesion","termid":"GO:0022407"},{"relation_name":"regulates","term_name":"calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules","termid":"GO:0016338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"regulation of calcium-independent cell-cell adhesion","termid":"GO:0051040"}


id: PBO:0039651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adaptor related protein complex 1 subunit mu 2","termid":"PBO:0039651"}


id: GO:0160120
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A mitochondrial complex that catalyzes the oxidative decarboxylation of branched-chain alpha-keto acids derived from L-leucine, L-isoleucine, and L-valine to branched-chain acyl-CoAs. The complex is organized around a 24-meric cubic core of the dihydrolipoyl transacylase (E2) with multiple (about 6 to 12) copies of the branched-chain alpha-ketoacid dehydrogenase (E1, consisting of alpha and beta subunits), about 6 copies of the dimeric dihydrolipoyl dehydrogenase (E3), and a small number of copies of the E1-specific kinase and phosphatase.","definition_xrefs":["PMID:9582350","PMID:10745006","PMID:3593587"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial branched-chain alpha-keto acid dehydrogenase complex (obsolete GO:0160120)","synonyms":[{"name":"BCKD complex","type":"exact"}],"termid":"GO:0160120"}


id: MONDO:0018397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete female infertility due to hypothalamic-pituitary-gonadal axis disorder (obsolete MONDO:0018397)","secondary_identifiers":["Orphanet:399831"],"synonyms":[{"name":"rare female infertility due to gonadotropic axis disorder","type":"exact"},{"name":"rare female infertility due to hypothalamic-pituitary-ovarian axis disorder","type":"exact"}],"termid":"MONDO:0018397","xrefs":{"Monarch":{"xref_id":"0018397"}}}


id: PBO:0059575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 2 pseudogene 1","termid":"PBO:0059575"}


id: PBO:0031516
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_binding","termid":"PBO:0031516"}


id: GO:1990912
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. 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 microwave radiation stimulus.","definition_xrefs":["PMID:21241601"],"gene_count":0,"genotype_count":0,"name":"obsolete response to microwave radiation (obsolete GO:1990912)","termid":"GO:1990912"}


id: PBO:0055278
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 2705","termid":"PBO:0055278"}


id: GO:0160145
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of GDF15-GFRAL signaling pathway.","definition_xrefs":["PMID:35177851"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"negatively_regulates","term_name":"GDF15-GFRAL signaling pathway","termid":"GO:0160144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of GDF15-GFRAL signaling pathway","termid":"GO:0160145"}


id: PBO:0003405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein intermediate chain Dic1","termid":"PBO:0003405"}


id: GO:0031868
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a prostaglandin F2-alpha receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostanoid receptor binding","termid":"GO:0031862"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"prostaglandin F2-alpha receptor binding","synonyms":[{"name":"prostaglandin F2-alpha receptor ligand","type":"narrow"},{"name":"prostanoid FP receptor binding","type":"exact"}],"termid":"GO:0031868"}


id: PBO:0068282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease H1 pseudogene 3","termid":"PBO:0068282"}


id: PBO:0092030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Tyrosine (gua), mitochondrial","termid":"PBO:0092030"}


id: GO:0042344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of indole glucosinolates, sulfur-containing compounds that have a common structure linked to an R group derived from tryptophan.","definition_xrefs":["PMID:29122987"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosinolate catabolic process","termid":"GO:0019762"},{"relation_name":"is_a","term_name":"indole glucosinolate metabolic process","termid":"GO:0042343"},{"relation_name":"is_a","term_name":"indole-containing compound catabolic process","termid":"GO:0042436"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006790","GO:0008150"],"is_obsolete":false,"name":"indole glucosinolate catabolic process","synonyms":[{"name":"indole glucosinolate breakdown","type":"exact"},{"name":"indole glucosinolate catabolism","type":"exact"},{"name":"indole glucosinolate degradation","type":"exact"}],"termid":"GO:0042344"}


id: PBO:0085022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nicotinic acid mononucleotide adenylyltransferase; catalyzes the transfer of the adenylyl moiety of ATP to nicotinamide mononucleotide to form NAD; involved in pathways of NAD biosynthesis, including the de novo, NAD(+) salvage, and nicotinamide riboside salvage pathways; homolog of human NMNAT; NMA1 has a paralog, NMA2, that arose from the whole genome duplication","termid":"PBO:0085022"}


id: PR:O42967
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1E8.02 gene.","definition_xrefs":["UniProtKB:O42967","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 ubiquitin-like protein C1E8.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1E8.02","synonyms":[{"name":"Spom972h-SPBC1E8.02","type":"exact"}],"termid":"PR:O42967"}


id: PBO:0039868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GTPase activating protein 27 pseudogene 2","termid":"PBO:0039868"}


id: PATO:0001077
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001077 absolute pressure (obsolete PATO:0001077)","termid":"PATO:0001077"}


id: MONDO:0018946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rhombencephalosynapsis (RS) is a rare malformation of the cerebellum characterized by the association of agenesis (total or partial) of the vermis and fusion of the cerebellar hemispheres.","definition_xrefs":["Orphanet:59315"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"rhombencephalosynapsis","secondary_identifiers":["icd11.foundation:2112180041","MEDGEN:356456","SCTID:442300000","GARD:18855","ICD9:742.4","UMLS:C1866130"],"termid":"MONDO:0018946","xrefs":{"Monarch":{"xref_id":"0018946"}}}


id: PBO:0089729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol-3-phosphate O-acyltransferase Sct1/Gpt1","termid":"PBO:0089729"}


id: PBO:0051444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 3-30 (pseudogene)","termid":"PBO:0051444"}


id: MONDO:0019809
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dysfunction of the aortic valve characterized by incomplete valve closure that is present at birth.","definition_xrefs":["NCIT:C103936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aortic valve insufficiency","termid":"MONDO:0005648"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"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 aortic valve insufficiency","secondary_identifiers":["UMLS:C0158617","MedDRA:10010370","ICD9:746.4","MEDGEN:510599","Orphanet:95449","SCTID:28656008"],"synonyms":[{"name":"Congential aortic valve insufficiency","type":"exact"},{"name":"congenital aortic insufficiency","type":"exact"},{"name":"congenital insufficiency of aortic valve","type":"exact"}],"termid":"MONDO:0019809","xrefs":{"Monarch":{"xref_id":"0019809"}}}


id: GO:0009923
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A tetrameric complex of four different subunits which catalyzes the elongation of a fatty acid chain 2 carbon units at a time in the synthesis of very long chain fatty acids.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"endoplasmic reticulum protein-containing complex","termid":"GO:0140534"},{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"},{"relation_name":"part_of","term_name":"endoplasmic reticulum membrane","termid":"GO:0005789"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"part_of","termid":"GO:0005789"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005783","GO:0032991","GO:0005737","GO:0005789","GO:0005575"],"is_obsolete":false,"name":"fatty acid elongase complex","termid":"GO:0009923"}


id: PBO:0091973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol-3-phosphate dehydrogenase Gut2","termid":"PBO:0091973"}


id: MONDO:0013079
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary biliary cholangitis","termid":"MONDO:0005388"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0019303","MONDO:0002515"],"is_obsolete":false,"name":"primary biliary cholangitis 2","secondary_identifiers":["MESH:C567817","DOID:0070359","OMIM:613007","UMLS:C2751696","GARD:15601","MEDGEN:442791"],"synonyms":[{"name":"PBC2","type":"related"},{"name":"biliary cirrhosis, primary, 2","type":"related"}],"termid":"MONDO:0013079","xrefs":{"Monarch":{"xref_id":"0013079"}}}


id: PBO:0028236
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-protein_mislocalized_to_nucleus_during_meiosis_I","termid":"PBO:0028236"}


id: FYECO:0000217
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells were grown for more than 24 hours.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping growth timing","termid":"FYECO:0000122"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth >24 hrs","synonyms":[{"name":"growth >24 hours","type":"exact"}],"termid":"FYECO:0000217"}


id: FYPO:0004556
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 phosphatidylcholine measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased cellular phosphatidylcholine level","synonyms":[{"name":"decreased cellular PC level","type":"exact"},{"name":"decreased cellular phosphatidylcholine level during mitotic cell cycle","type":"related"},{"name":"decreased cellular phosphatidylcholine level during vegetative growth","type":"exact"},{"name":"decreased phosphatidylcholine accumulation","type":"related"},{"name":"reduced cellular phosphatidylcholine level","type":"exact"}],"termid":"FYPO:0004556"}


id: PR:P40997
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ceg1 gene.","definition_xrefs":["UniProtKB:P40997","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":"mRNA-capping enzyme subunit alpha (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2F12.08c","synonyms":[{"name":"GTP--RNA guanylyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"GTase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ceg1","type":"exact"},{"name":"mRNA guanylyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P40997"}


id: GO:0015107
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of chlorate, ClO3-, from one side of a membrane to the other.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inorganic anion transmembrane transporter activity","termid":"GO:0015103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"chlorate transmembrane transporter activity","termid":"GO:0015107"}


id: GO:0002769
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by an extracellular ligand binding to a receptor on the surface of a natural killer cell capable of inhibiting an immune effector process contributing to an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add","PMID:15771571"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune response-inhibiting cell surface receptor signaling pathway","termid":"GO:0002767"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"natural killer cell inhibitory signaling pathway","synonyms":[{"name":"Ly49 inhibitory receptor signaling pathway","type":"related"},{"name":"NK cell inhibitory signaling pathway","type":"exact"},{"name":"inhibitory KIR signaling pathway","type":"narrow"},{"name":"killer cell inhibitory receptor signaling pathway","type":"narrow"},{"name":"natural killer cell inhibitory signalling pathway","type":"exact"}],"termid":"GO:0002769"}


id: PBO:0071792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease P/MRP subunit p38","termid":"PBO:0071792"}


id: GO:0044788
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a host organism modulates the frequency, rate or extent of any of a process being mediated by a virus with which it is infected.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host-mediated perturbation of symbiont process","termid":"GO:0051851"}],"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":"modulation by host of viral process","termid":"GO:0044788"}


id: PBO:0091427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenase","termid":"PBO:0091427"}


id: RO:0002576
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of has skeleton","direct_ancestors":[{"relation_name":"is_a","term_name":"part_of","termid":"BFO:0000050"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"skeleton_of","termid":"RO:0002576"}


id: GO:1990082
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that inhibits unwinding of DNA at the origin of replication and assembly of the pre-primosome. In E. coli, this complex is composed of DnaA and of the ribosomal protein L2.","definition_xrefs":["GOC:bhm","PMID:21288885"],"direct_ancestors":[{"relation_name":"is_a","term_name":"replication inhibiting complex","termid":"GO:1990078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005694","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"DnaA-L2 complex","termid":"GO:1990082"}


id: GO:0170013
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that spans a membrane and forms a water-filled channel across the phospholipid bilayer allowing selective ion transport down its electrochemical gradient.","definition_xrefs":["PMID:10839820"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"channel complex","termid":"GO:0170013"}


id: MONDO:0015236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital abnormalities of the aortic arch result from aberrant development of one or more components of the embyronic pharangeal arch system. Any component of this system can regress or persist abnormally, resulting in an extensive array of aortic arch anomalies. Clinically, they are classified by those that cause (or are likely to cause) physiolgogical abnormalities and those that do not. Physiologic abnormalities include tracheobronchial compression, esophageeal compression, and abnormal blood flow patteren.","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital anomaly of the great arteries","termid":"MONDO:0020292"},{"relation_name":"is_a","term_name":"branchial arch disease","termid":"MONDO:0022606"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aortic arch defects","secondary_identifiers":["Orphanet:1132","UMLS:C5680872","MEDGEN:1842770","GARD:741"],"termid":"MONDO:0015236","xrefs":{"Monarch":{"xref_id":"0015236"}}}


id: PR:O14202
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug116 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14202"],"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 116 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5D6.10c","synonyms":[{"name":"Spom972h-mug116","type":"exact"}],"termid":"PR:O14202"}


id: GO:0160112
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A structural network of microtubule inner proteins (MIPs) located inside the lumen of the B tubule of the axonemal microtubule doublet that helps stabilize the B tubule.","definition_xrefs":["GOC:krc","PMID:37295417","PMID:29430673"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"A axonemal microtubule","termid":"GO:0097649"},{"relation_name":"part_of","term_name":"axonemal microtubule doublet inner sheath","termid":"GO:0160110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0015630"],"is_obsolete":false,"name":"axonemal B tubule inner sheath","termid":"GO:0160112"}


id: PBO:0065166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein interacting with cyclin A1","termid":"PBO:0065166"}


id: GO:0005248
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a sodium ion by a voltage-gated channel. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium channel activity","termid":"GO:0005272"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"voltage-gated sodium channel activity","secondary_identifiers":["Reactome:R-HSA-5576895"],"synonyms":[{"name":"voltage gated sodium channel activity","type":"exact"},{"name":"voltage-dependent sodium channel activity","type":"exact"},{"name":"voltage-gated sodium ion channel activity","type":"exact"},{"name":"voltage-sensitive sodium channel","type":"exact"}],"termid":"GO:0005248"}


id: GO:0098932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disruption by a symbiont of host cell wall peptidoglycans to allow entry into the host cell.","definition_xrefs":["VZ:3940","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated disruption of host cell wall","termid":"GO:0052009"},{"relation_name":"part_of","term_name":"symbiont entry into host cell","termid":"GO:0046718"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont entry into host cell via disruption of host cell wall peptidoglycan","synonyms":[{"name":"catabolism of host cell wall peptidoglycan by virus","type":"exact"},{"name":"degradation of host cell wall peptidoglycan by virus","type":"exact"},{"name":"degradation of host peptidoglycans during virus entry","type":"exact"},{"name":"disassembly by virus of host cell wall peptidoglycan","type":"exact"},{"name":"disruption by virus of host cell wall peptidoglycan during virus entry","type":"exact"}],"termid":"GO:0098932"}


id: MONDO:0002392
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lymphangiosarcoma (obsolete MONDO:0002392)","termid":"MONDO:0002392","xrefs":{"Monarch":{"xref_id":"0002392"}}}


id: PBO:0085262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Permease identified in lager brewing yeast strain Weihenstephan Nr.34; also in RM11-1a, but not S288C; subject to nitrogen catabolite repression and post-translational control, cellular localization dependent on nitrogen source quality","termid":"PBO:0085262"}


id: GO:0052193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of an organism or motile cell on, within or near its symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete movement in symbiont environment (obsolete GO:0052193)","termid":"GO:0052193"}


id: PBO:0082216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha 5 subunit of the 20S proteasome; involved in ubiquitin-dependent catabolism; human homolog is subunit zeta","termid":"PBO:0082216"}


id: GO:0048003
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigen-presenting cell expresses lipid antigen in association with an MHC class Ib protein complex on its cell surface, including lipid extraction, degradation, and transport steps for the lipid antigen both prior to and following assembly with the MHC protein complex. The lipid antigen may originate from an endogenous or exogenous source of lipid. Class Ib here refers to non-classical class I molecules, such as those of the CD1 family.","definition_xrefs":["GOC:add","PMID:10375559","PMID:15928680","PMID:15928678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation via MHC class Ib","termid":"GO:0002475"}],"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":"antigen processing and presentation of lipid antigen via MHC class Ib","synonyms":[{"name":"antigen presentation, lipid antigen","type":"exact"},{"name":"lipid antigen processing and presentation via MHC class Ib","type":"exact"}],"termid":"GO:0048003"}


id: PR:O60081
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trm72 gene.","definition_xrefs":["UniProtKB:O60081","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 C1494.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1494.07","synonyms":[{"name":"Spom972h-trm72","type":"exact"}],"termid":"PR:O60081"}


id: GO:1903594
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of histamine secretion by mast cell.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:18253931","GOC:als"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hormone secretion","termid":"GO:0046888"},{"relation_name":"is_a","term_name":"negative regulation of inflammatory response","termid":"GO:0050728"},{"relation_name":"is_a","term_name":"regulation of histamine secretion by mast cell","termid":"GO:1903593"},{"relation_name":"negatively_regulates","term_name":"histamine secretion by mast cell","termid":"GO:0002553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of histamine secretion by mast cell","synonyms":[{"name":"down regulation of histamine secretion by mast cell","type":"exact"},{"name":"down-regulation of histamine secretion by mast cell","type":"exact"},{"name":"downregulation of histamine secretion by mast cell","type":"exact"},{"name":"inhibition of histamine secretion by mast cell","type":"narrow"}],"termid":"GO:1903594"}


id: GO:0014046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of dopamine by a cell. Dopamine is a catecholamine and a precursor of adrenaline and noradrenaline. It acts as a neurotransmitter in the central nervous system but it is also produced peripherally and acts as a hormone.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dopamine transport","termid":"GO:0015872"},{"relation_name":"is_a","term_name":"signal release","termid":"GO:0023061"},{"relation_name":"is_a","term_name":"catecholamine secretion","termid":"GO:0050432"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"dopamine secretion","termid":"GO:0014046"}


id: GO:0075344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The alteration by an organism of protein levels in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by symbiont of host protein levels (obsolete GO:0075344)","termid":"GO:0075344"}


id: FYPO:0006515
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which telomere length is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal telomere morphology","termid":"FYPO:0006512"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal telomere length","termid":"FYPO:0006515"}


id: PBO:0113192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Major CTP synthase isozyme (see also URA8); catalyzes ATP-dependent transfer of amide nitrogen from glutamine to UTP, forming CTP, final step in de novo biosynthesis of pyrimidines; involved in phospholipid biosynthesis; targeted to vacuole via AP-3 pathway; capable of forming cytoplasmic filaments termed cytoophidium, especially during conditions of glucose depletion; URA7 has paralog URA8 that arose from the whole genome duplication","termid":"PBO:0113192"}


id: PBO:0086957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulator of peroxisome abundance; peroxisomal membrane protein, remote homolog to several curvature-generating human proteins; functionally interacts with vesicle-budding-inducing ADP-ribosylation factor Arf1p","termid":"PBO:0086957"}


id: MONDO:0003849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A slow-growing malignant bone tumor arising from the remnants of the notochord and occurring in the clivus. It is characterized by a lobulated growth pattern, myxoid stroma formation, and the presence of physaliphorous cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skull base chordoma","termid":"MONDO:0002892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"clivus chordoma","secondary_identifiers":["ICD9:170.0","NCIT:C5412","MEDGEN:232372","SCTID:446939001","UMLS:C1333071","DOID:6312"],"synonyms":[{"name":"chordoma (disease) of clivus of occipital bone","type":"exact"},{"name":"chordoma of clivus","type":"exact"},{"name":"chordoma of the clivus","type":"exact"},{"name":"clival chordoma","type":"exact"},{"name":"clivus of occipital bone chordoma (disease)","type":"exact"}],"termid":"MONDO:0003849","xrefs":{"Monarch":{"xref_id":"0003849"}}}


id: MONDO:0006972
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of alveolitis or pneumonitis caused by hypersensitivity to high level of inhaled nitrogen oxides, decomposition products of silage.","definition_xrefs":["MESH:D012832"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung disorder","termid":"MONDO:0005275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"silo filler disease","secondary_identifiers":["SCTID:61233003","MEDGEN:11428","icd11.foundation:1960063586","UMLS:C0037120","DOID:4374"],"synonyms":[{"name":"silo filler disease","type":"exact"},{"name":"silo filler's disease","type":"related"},{"name":"silo-fillers' disease","type":"exact"}],"termid":"MONDO:0006972","xrefs":{"Monarch":{"xref_id":"0006972"}}}


id: GO:0046095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of deoxyinosine, hypoxanthine deoxyriboside.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyinosine metabolic process","termid":"GO:0046094"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside biosynthetic process","termid":"GO:0046123"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"deoxyinosine biosynthetic process","synonyms":[{"name":"deoxyinosine anabolism","type":"exact"},{"name":"deoxyinosine biosynthesis","type":"exact"},{"name":"deoxyinosine formation","type":"exact"},{"name":"deoxyinosine synthesis","type":"exact"}],"termid":"GO:0046095"}


id: PBO:0079210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis specific serine kinase 2","termid":"PBO:0079210"}


id: PBO:0056731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MEST intronic transcript 1, antisense RNA","termid":"PBO:0056731"}


id: PR:000050485
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A Ras GTPase-activating-like protein rng2 (Schizosaccharomyces pombe) that has not been phosphorylated at the positions equivalent to Ser-199 and Ser-207 of the amino acid sequence represented by UniProtKB:O14188. Example: UniProtKB:O14188, Ser-199/Ser-207, PR:000026291.","definition_xrefs":["PMID:33131769","PRO:DAN","PomBase:VW"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ras GTPase-activating-like protein rng2 (Schizosaccharomyces pombe)","termid":"PR:000050483"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rng2/UnPhos(S199,S207)","pombase_gene_id":"SPAC4F8.13c","synonyms":[{"name":"PomBase_original_PRO_term_name: Ras GTPase-activating-like protein rng2 unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-rng2/UnPhos:1","type":"exact"},{"name":"UniProtKB:O14188, Ser-199/Ser-207, PR:000026291","type":"narrow"},{"name":"rng2/UnPhos(S199,S207)","type":"exact"}],"termid":"PR:000050485"}


id: MONDO:0009301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46,XY complete gonadal dysgenesis","termid":"MONDO:0010765"}],"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":"46,XY sex reversal 7","secondary_identifiers":["UMLS:C1856273","DOID:0111774","GARD:15174","MEDGEN:383876","OMIM:233420","MESH:C565537"],"synonyms":[{"name":"46,XY SEX reversal 7","type":"related"},{"name":"46,XY Sex reversal type 7","type":"exact"},{"name":"46,XY Sex reversal, partial or complete, Dhh-related","type":"related"},{"name":"46,XY gonadal dysgenesis, partial or complete, Dhh-related","type":"related"},{"name":"46,XY sex reversal 7","type":"exact"},{"name":"46XY sex reversal 7","type":"exact"},{"name":"SRXY7","type":"related"},{"name":"gonadal dysgenesis, XY, Male-limited","type":"related"}],"termid":"MONDO:0009301","xrefs":{"Monarch":{"xref_id":"0009301"}}}


id: PBO:0059388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S23 pseudogene 1","termid":"PBO:0059388"}


id: GO:0090295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transcription regulation process in which the presence of one nitrogen source leads to a decrease in the frequency, rate, or extent of transcription of specific genes involved in the metabolism of other nitrogen sources.","definition_xrefs":["GOC:mah","GOC:rb","PMID:19104072"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of DNA-templated transcription","termid":"GO:0045892"},{"relation_name":"is_a","term_name":"catabolite repression","termid":"GO:0061984"},{"relation_name":"is_a","term_name":"nitrogen catabolite regulation of transcription","termid":"GO:0090293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006351","GO:0008150","GO:0006355","GO:0010467"],"is_obsolete":false,"name":"nitrogen catabolite repression of transcription","synonyms":[{"name":"negative regulation of transcription by nitrogen catabolites","type":"exact"},{"name":"nitrogen catabolite repression","type":"exact"}],"termid":"GO:0090295"}


id: PBO:0074937
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 103B","termid":"PBO:0074937"}


id: GO:0006257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of dUDP, deoxyuridine (5'-)diphosphate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside diphosphate catabolic process","termid":"GO:0009198"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleotide catabolic process","termid":"GO:0009223"},{"relation_name":"is_a","term_name":"dUDP metabolic process","termid":"GO:0046077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"dUDP catabolic process","synonyms":[{"name":"dUDP breakdown","type":"exact"},{"name":"dUDP catabolism","type":"exact"},{"name":"dUDP degradation","type":"exact"}],"termid":"GO:0006257"}


id: PBO:0000166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-methyl-2-oxobutanoatehydroxymethyltransferase(predicted)","termid":"PBO:0000166"}


id: PBO:0073168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secreted and transmembrane 1","termid":"PBO:0073168"}


id: PBO:0089544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Set1C complex WD repeat protein Swd3","termid":"PBO:0089544"}


id: PBO:0062091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily A member 41 pseudogene","termid":"PBO:0062091"}


id: GO:0015325
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA(out) + CoA(in) = acetyl-CoA(in) + CoA(out).","definition_xrefs":["TC:2.A.1.25.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetyl-CoA transmembrane transporter activity","termid":"GO:0008521"},{"relation_name":"is_a","term_name":"coenzyme A transmembrane transporter activity","termid":"GO:0015228"},{"relation_name":"is_a","term_name":"antiporter activity","termid":"GO:0015297"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"acetyl-CoA:CoA antiporter activity","termid":"GO:0015325"}


id: PBO:0091318
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Recovery of STe11 expression","termid":"PBO:0091318"}


id: GO:0005276
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of a solute or solutes from one side of a vesicle membrane to the other according to the reaction: H+(in) + amino acid(out) = H+(out) + amino acid(in).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete vesicular amino acid:proton antiporter activity (obsolete GO:0005276)","synonyms":[{"name":"hydrogen:vesicular amine antiporter activity","type":"exact"},{"name":"vesicular hydrogen:amino acid antiporter activity","type":"exact"}],"termid":"GO:0005276"}


id: MONDO:0003665
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cervical adenocarcinoma with the histologic characteristics of the endometrioid adenocarcinoma of the endometrium.","definition_xrefs":["NCIT:C6343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrioid adenocarcinoma","termid":"MONDO:0005026"},{"relation_name":"is_a","term_name":"cervical adenocarcinoma","termid":"MONDO:0005153"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"cervical endometrioid adenocarcinoma","secondary_identifiers":["ONCOTREE:CEEN","EFO:1000164","DOID:5830","MEDGEN:272450","UMLS:C1332913"],"synonyms":[{"name":"cervical endometrioid adenocarcinoma","type":"exact"},{"name":"cervical endometrioid carcinoma","type":"exact"},{"name":"cervix endometrioid adenocarcinoma","type":"exact"},{"name":"cervix endometrioid carcinoma","type":"exact"},{"name":"cervix uteri endometrioid adenocarcinoma","type":"exact"},{"name":"cervix uteri endometrioid carcinoma","type":"exact"},{"name":"endometrioid adenocarcinoma of cervix","type":"exact"},{"name":"endometrioid adenocarcinoma of cervix uteri","type":"exact"},{"name":"endometrioid adenocarcinoma of the cervix","type":"exact"},{"name":"endometrioid adenocarcinoma of the cervix uteri","type":"exact"},{"name":"endometrioid adenocarcinoma of the uterine cervix","type":"exact"},{"name":"endometrioid adenocarcinoma of uterine cervix","type":"exact"},{"name":"endometrioid carcinoma of cervix","type":"exact"},{"name":"endometrioid carcinoma of cervix uteri","type":"exact"},{"name":"endometrioid carcinoma of the cervix","type":"exact"},{"name":"endometrioid carcinoma of the cervix uteri","type":"exact"},{"name":"endometrioid carcinoma of the uterine cervix","type":"exact"},{"name":"endometrioid carcinoma of uterine cervix","type":"exact"},{"name":"uterine cervix endometrioid adenocarcinoma","type":"exact"},{"name":"uterine cervix endometrioid carcinoma","type":"exact"}],"termid":"MONDO:0003665","xrefs":{"Monarch":{"xref_id":"0003665"}}}


id: FYPO:0000272
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A septation phenotype observed in the vegetative growth phase of the life cycle in which a cell fails to form a septum.","definition_xrefs":["PMID:9649519","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal septum assembly","termid":"FYPO:0000117"},{"relation_name":"is_a","term_name":"abolished cytokinesis","termid":"FYPO:0000417"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0001320","FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abolished septum assembly","synonyms":[{"name":"abolished division septum assembly","type":"exact"},{"name":"abolished septation","type":"broad"},{"name":"abolished septum assembly during mitotic cell cycle","type":"related"},{"name":"abolished septum formation","type":"exact"},{"name":"septum assembly abolished","type":"exact"},{"name":"septum assembly abolished during vegetative growth","type":"exact"},{"name":"septum formation: absent","type":"related"},{"name":"septum initiation defective","type":"related"}],"termid":"FYPO:0000272"}


id: _global:has_role
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"a relation between an independent continuant (the bearer) and a role, in which the role specifically depends on the bearer for its existence","direct_ancestors":[{"relation_name":"is_a","term_name":"has_characteristic","termid":"_global:has_characteristic"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_role","secondary_identifiers":["RO:0000087"],"termid":"_global:has_role"}


id: GO:0030223
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a myeloid precursor cell acquires the specialized features of a neutrophil.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"granulocyte differentiation","termid":"GO:0030851"}],"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":"neutrophil differentiation","synonyms":[{"name":"neutrophil cell differentiation","type":"exact"},{"name":"neutrophil granulocyte differentiation","type":"exact"},{"name":"neutrophil granulocytopoiesis","type":"exact"}],"termid":"GO:0030223"}


id: PBO:0075753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRP receptor subunit beta","termid":"PBO:0075753"}


id: GO:0035065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the addition of an acetyl group to a histone protein.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone acetylation (obsolete GO:0035065)","termid":"GO:0035065"}


id: PBO:0049389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP binding protein 2","termid":"PBO:0049389"}


id: MONDO:0007577
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":"esophageal ring, lower","secondary_identifiers":["ICD9:750.3","OMIM:133240","UMLS:C0341137","SCTID:235623002","MEDGEN:83320","MESH:C562765"],"synonyms":[{"name":"esophageal ring, lower","type":"exact"}],"termid":"MONDO:0007577","xrefs":{"Monarch":{"xref_id":"0007577"}}}


id: FYPO:0000402
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of progression through the G2/M transition of the mitotic cell cycle is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic G2/M phase transition","termid":"FYPO:0000399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased mitotic G2/M phase transition","synonyms":[{"name":"cell cycle progression through the G2/M phase transition: increased","type":"related"},{"name":"increased G2/M phase transition during mitotic cell cycle","type":"exact"},{"name":"increased cell cycle progression through mitotic G2/M phase transition","type":"exact"},{"name":"increased occurrence of mitotic G2/M phase transition during vegetative growth","type":"exact"}],"termid":"FYPO:0000402"}


id: SO:0001385
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A post translationally modified amino acid feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_amino_acid_feature","synonyms":[{"name":"modified amino acid feature","type":"exact"}],"termid":"SO:0001385"}


id: PBO:0068479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 58, pseudogene","termid":"PBO:0068479"}


id: PBO:0001579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-3 adaptor complex subunit Apl6 (predicted)","termid":"PBO:0001579"}


id: PBO:0028114
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-snoRNA_guided_rRNA_2'-O-methylation_abolished_at_specific_site","termid":"PBO:0028114"}


id: PBO:0070244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 185 pseudogene","termid":"PBO:0070244"}


id: MONDO:0017122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature (obsolete MONDO:0017122)","secondary_identifiers":["Orphanet:269573"],"termid":"MONDO:0017122","xrefs":{"Monarch":{"xref_id":"0017122"}}}


id: GO:0010624
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency or rate of multiplication or reproduction of Schwann cells, resulting in the expansion of their population. Schwann cells are a type of glial cell in the peripheral nervous system.","definition_xrefs":["GOC:sl","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glial cell proliferation","termid":"GO:0060251"},{"relation_name":"regulates","term_name":"Schwann cell proliferation","termid":"GO:0014010"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of Schwann cell proliferation","termid":"GO:0010624"}


id: FYPO_EXT:0000004
data:
  {"annotation_feature_type":"gene","cv_name":"fypo_extensions","definition":"all cells (penetrance)","definition_xrefs":["PomBase:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"FYPO penetrance extension","termid":"FYPO_EXT:1000002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complete","synonyms":[{"name":"100%","type":"exact"},{"name":"full","type":"exact"}],"termid":"FYPO_EXT:0000004"}


id: MONDO:0001858
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic painful nonsuppurative swellings of one or more costal cartilages, especially of the second rib. The anterior chest pain may mimic that of coronary artery disease.","definition_xrefs":["MESH:D013991"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"arthropathy","termid":"MONDO:0006816"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tietze syndrome","secondary_identifiers":["SCTID:30128009","UMLS:C0040213","MEDGEN:52753","NCIT:C168333","DOID:14021","ICD9:733.6"],"synonyms":[{"name":"Chondropathia tuberosa","type":"related"},{"name":"Costalchondritis","type":"exact"},{"name":"Costochondritis","type":"exact"},{"name":"Tietze syndrome","type":"exact"},{"name":"Tietze's disease","type":"exact"},{"name":"Tietze's syndrome","type":"exact"},{"name":"costochondral joint syndromic disease","type":"exact"},{"name":"costochondral junction syndrome","type":"exact"},{"name":"slipping rib syndrome","type":"exact"},{"name":"syndromic disease of costochondral joint","type":"exact"}],"termid":"MONDO:0001858","xrefs":{"Monarch":{"xref_id":"0001858"}}}


id: GO:1990239
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a steroid hormone.","definition_xrefs":["GOC:ln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid binding","termid":"GO:0005496"},{"relation_name":"is_a","term_name":"hormone binding","termid":"GO:0042562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0008289"],"is_obsolete":false,"name":"steroid hormone binding","termid":"GO:1990239"}


id: GO:0033868
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + Goodpasture antigen-binding protein = ADP + Goodpasture antigen-binding phosphoprotein.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete Goodpasture-antigen-binding protein kinase activity (obsolete GO:0033868)","termid":"GO:0033868"}


id: MONDO:0012068
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":"brachial palsy, familial congenital","secondary_identifiers":["UMLS:C1837810","MEDGEN:324884","OMIM:608585","MESH:C563901"],"synonyms":[{"name":"brachial palsy, familial congenital","type":"exact"}],"termid":"MONDO:0012068","xrefs":{"Monarch":{"xref_id":"0012068"}}}


id: PBO:0047401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 39","termid":"PBO:0047401"}


id: GO:0016129
data:
  {"annotated_genes":["SJAG_04499","SJAG_00717","SJAG_00453","SJAG_02982","SJAG_03509","SJAG_04217","SJAG_02855","SJAG_01474","SJAG_03715","SJAG_03235","SJAG_03598","SJAG_02104","SJAG_03531","SJAG_03249","SJAG_02719","SJAG_00413","SJAG_00624","SJAG_03929","SJAG_00370","SJAG_03750","SJAG_04270","SJAG_03024","SJAG_04810","SJAG_04018","SJAG_02044","SJAG_00770","SJAG_03018","SJAG_01307"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118568,75728,76073,91539,109819,82102,72680,71606,73505,78279,82128,67109,73299,90346,81916,74922,111235,78271,96540,109505,117252,79008,77914,112077],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006696"},{"annotations":[95777],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0010895"},{"annotations":[111843],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0070452"},{"annotations":[90435,107806],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032443"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phytosteroids, steroids that differ from animal steroids in having substitutions at C24 and/or a double bond at C22. Phytosteroids are so named because they occur in higher plants; some, notably ergosterol, are also found in fungi.","definition_xrefs":["GOC:mah","GOC:go_curators","ISBN:0471331309"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid biosynthetic process","termid":"GO:0006694"},{"relation_name":"is_a","term_name":"phytosteroid metabolic process","termid":"GO:0016128"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00370":null,"SJAG_00413":null,"SJAG_00453":null,"SJAG_00624":null,"SJAG_00717":null,"SJAG_00770":null,"SJAG_01307":null,"SJAG_01474":null,"SJAG_02044":null,"SJAG_02104":null,"SJAG_02719":null,"SJAG_02855":null,"SJAG_02982":null,"SJAG_03018":null,"SJAG_03024":null,"SJAG_03235":null,"SJAG_03249":null,"SJAG_03509":null,"SJAG_03531":null,"SJAG_03598":null,"SJAG_03715":null,"SJAG_03750":null,"SJAG_03929":null,"SJAG_04018":null,"SJAG_04217":null,"SJAG_04270":null,"SJAG_04499":null,"SJAG_04810":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"phytosteroid biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"phytosteroid anabolism","type":"exact"},{"name":"phytosteroid biosynthesis","type":"exact"},{"name":"phytosteroid formation","type":"exact"},{"name":"phytosteroid synthesis","type":"exact"}],"termid":"GO:0016129","terms_by_termid":{"GO:0006696":null,"GO:0010895":null,"GO:0032443":null,"GO:0070452":null}}


id: PBO:0045447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPYD intronic transcript 1","termid":"PBO:0045447"}


id: PBO:0086904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative type-1 protein phosphatase targeting subunit; tethers Glc7p type-1 protein phosphatase to Gsy2p glycogen synthase; PIG2 has a paralog, GIP2, that arose from the whole genome duplication","termid":"PBO:0086904"}


id: PATO:0002506
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A surface feature shape quality inhering in a bearer by virtue of the bearer's not having undulating edges forming lobes.","definition_xrefs":["PATOC:DOS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"surface feature shape","termid":"PATO:0001925"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alobate","termid":"PATO:0002506"}


id: MONDO:0017754
data:
  {"annotated_genes":["SJAG_02896","SJAG_01372","SJAG_03961","SJAG_02876","SJAG_00938","SJAG_03011","SJAG_05283","SJAG_01344","SJAG_04109","SJAG_03785","SJAG_03363","SJAG_05213","SJAG_04944","SJAG_05194","SJAG_01841"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008294"},{"annotations":[88375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008822"},{"annotations":[88636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011559"},{"annotations":[88834,88835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030810"},{"annotations":[87710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031040"},{"annotations":[87294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009902"},{"annotations":[87140,87139,87138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009380"},{"annotations":[87550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008296"},{"annotations":[87249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030048"},{"annotations":[87702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007369"},{"annotations":[87295],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013000"},{"annotations":[88766],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011156"},{"annotations":[87376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011214"},{"annotations":[86986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008319"},{"annotations":[87569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008297"},{"annotations":[88221],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957577"},{"annotations":[88566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010420"},{"annotations":[88564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020721"}]},"cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of porphyrin-containing compound metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"porphyrin metabolism disease","termid":"MONDO:0037821"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_01344":null,"SJAG_01372":null,"SJAG_01841":null,"SJAG_02876":null,"SJAG_02896":null,"SJAG_03011":null,"SJAG_03363":null,"SJAG_03785":null,"SJAG_03961":null,"SJAG_04109":null,"SJAG_04944":null,"SJAG_05194":null,"SJAG_05213":null,"SJAG_05283":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"inborn disorder of porphyrin metabolism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:E80.4","GARD:21346","Orphanet:309813","SCTID:403832004"],"synonyms":[{"name":"disorder of porphyrin and haem metabolism","type":"broad"},{"name":"inborn disorder of porphyrin and haem metabolism","type":"exact"},{"name":"inborn error of porphyrin-containing compound metabolic process","type":"exact"},{"name":"inborn porphyrin-containing compound metabolic process disorder","type":"exact"},{"name":"inherited disorder of porphyrin metabolism","type":"exact"},{"name":"rare inborn error of porphyrin-containing compound metabolic process","type":"exact"}],"termid":"MONDO:0017754","terms_by_termid":{"MONDO:0007369":null,"MONDO:0008294":null,"MONDO:0008296":null,"MONDO:0008297":null,"MONDO:0008319":null,"MONDO:0008822":null,"MONDO:0009380":null,"MONDO:0009902":null,"MONDO:0010420":null,"MONDO:0011156":null,"MONDO:0011214":null,"MONDO:0011559":null,"MONDO:0013000":null,"MONDO:0020721":null,"MONDO:0030048":null,"MONDO:0030810":null,"MONDO:0031040":null,"MONDO:0957577":null},"xrefs":{"Monarch":{"xref_id":"0017754"}}}


id: PBO:0113040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chaperone for eEF1A; ribosome-associated chaperone dedicated to facilitating high-level expression of eEF1A; transiently binds nascent GTPase domain of eEF1A as soon as it emerges from ribosome tunnel; forms complex with NAC by binding UBA domain of Egd2p; inactivation results in disturbed proteostasis and Hsf1p activation due to abberant eEF1A biogenesis; overlapping phenotypes support notion that Chp1p functions in same eEF1A biogenesis pathway as chaperone Zpr1p-Aim29p","termid":"PBO:0113040"}


id: PBO:0114420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AIF family member 3","termid":"PBO:0114420"}


id: MONDO:0006898
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the tissues around a joint. (Dorland, 27th ed)","definition_xrefs":["MESH:D010489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bursitis","termid":"MONDO:0002471"},{"relation_name":"is_a","term_name":"arthritic joint disease","termid":"MONDO:0005578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"periarthritis","secondary_identifiers":["SCTID:50921008","EFO:1001097","MedDRA:10034464","DOID:2964","UMLS:C0031037","MEDGEN:45397"],"termid":"MONDO:0006898","xrefs":{"Monarch":{"xref_id":"0006898"}}}


id: MONDO:0700156
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Soft tissue sarcoma occurring in a dog.","definition_xrefs":["NCIT:C132276"],"direct_ancestors":[{"relation_name":"is_a","term_name":"canine sarcoma","termid":"MONDO:0700149"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canine soft tissue sarcoma","termid":"MONDO:0700156","xrefs":{"Monarch":{"xref_id":"0700156"}}}


id: FYPO:0001747
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 nickel ions into a cell is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal nickel import","synonyms":[{"name":"abnormal cellular nickel import","type":"exact"},{"name":"abnormal nickel cation import","type":"exact"},{"name":"abnormal nickel import across plasma membrane","type":"exact"},{"name":"abnormal nickel import during mitotic cell cycle","type":"related"},{"name":"abnormal nickel import during vegetative growth","type":"exact"},{"name":"abnormal nickel import into cell","type":"exact"},{"name":"abnormal nickel ion import","type":"exact"}],"termid":"FYPO:0001747"}


id: PBO:0068963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 207, pseudogene","termid":"PBO:0068963"}


id: GO:0060526
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the prostate glandular acini are generated and organized. The glandular acini are the saclike structures of the gland.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostate gland epithelium morphogenesis","termid":"GO:0060740"},{"relation_name":"part_of","term_name":"prostate glandular acinus development","termid":"GO:0060525"}],"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":"prostate glandular acinus morphogenesis","termid":"GO:0060526"}


id: PBO:0025551
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"combined malonic and methylmalonic aciduria","termid":"PBO:0025551"}


id: GO:1900325
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of maltotriulose 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 maltotriulose transport","termid":"GO:1900324"},{"relation_name":"negatively_regulates","term_name":"maltotriulose transport","termid":"GO:2001090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of maltotriulose transport","synonyms":[{"name":"down regulation of maltotriulose transport","type":"exact"},{"name":"down-regulation of maltotriulose transport","type":"exact"},{"name":"downregulation of maltotriulose transport","type":"exact"},{"name":"inhibition of maltotriulose transport","type":"narrow"}],"termid":"GO:1900325"}


id: MONDO:0017979
data:
  {"annotated_genes":["SJAG_01787","SJAG_03453","SJAG_00610"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013767"},{"annotations":[87653,87652],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000024"}]},"cv_name":"mondo","definition":"Autoimmune lymphoproliferative syndrome (ALPS) is a rare, inherited disorder characterized by non-malignant lymphoproliferation, multilineage cytopenias, and a lifelong increased risk of Hodgkin's and non-Hodgkin's lymphoma.","definition_xrefs":["Orphanet:3261"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lymphoid hemopathy","termid":"MONDO:0015757"},{"relation_name":"is_a","term_name":"type IV hypersensitivity disease","termid":"MONDO:0002459"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"},{"relation_name":"is_a","term_name":"lymphoproliferative syndrome","termid":"MONDO:0016537"},{"relation_name":"is_a","term_name":"neoplastic syndrome","termid":"MONDO:0021058"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune lymphoproliferative syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2200726","GARD:8686","NANDO:1200352","MESH:D056735","MedDRA:10069521","CSP:1560-5548","ICD9:279.41","NCIT:C37864","icd11.foundation:1072688797","DOID:6688"],"synonyms":[{"name":"ALPS","type":"exact"},{"name":"ALPS (autoimmune lymphoproliferative syndrome)","type":"exact"},{"name":"Canale-Smith syndrome","type":"exact"},{"name":"FAS deficiency","type":"exact"},{"name":"autoimmune lymphoproliferative syndrome type 1, autosomal dominant","type":"related"}],"termid":"MONDO:0017979","terms_by_termid":{"MONDO:0013767":null,"MONDO:8000024":null},"xrefs":{"Monarch":{"xref_id":"0017979"}}}


id: PBO:0062356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily Q member 1","termid":"PBO:0062356"}


id: PBO:0087019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribose-5-phosphate ketol-isomerase; catalyzes the interconversion of ribose 5-phosphate and ribulose 5-phosphate in the pentose phosphate pathway; participates in pyridoxine biosynthesis","termid":"PBO:0087019"}


id: MONDO:1012532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"calvarial hyperostotic syndrome, non-human animal","termid":"MONDO:1011658"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calvarial hyperostotic syndrome, dog","secondary_identifiers":["OMIA:002245-9615"],"termid":"MONDO:1012532","xrefs":{"Monarch":{"xref_id":"1012532"}}}


id: GO:0010700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the regulated release of norepinephrine.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of norepinephrine secretion","termid":"GO:0014061"},{"relation_name":"is_a","term_name":"negative regulation of catecholamine secretion","termid":"GO:0033604"},{"relation_name":"negatively_regulates","term_name":"norepinephrine secretion","termid":"GO:0048243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of norepinephrine secretion","termid":"GO:0010700"}


id: PBO:0066314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding protein, mRNA processing factor","termid":"PBO:0066314"}


id: MONDO:0018368
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian serous adenocarcinoma","termid":"MONDO:0005211"},{"relation_name":"is_a","term_name":"primary peritoneal serous adenocarcinoma","termid":"MONDO:0006386"}],"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":"primary peritoneal serous/papillary carcinoma","secondary_identifiers":["Orphanet:398980","NCIT:C7695","UMLS:C1368918","GARD:21653","DOID:6228","MEDGEN:237154"],"synonyms":[{"name":"PPSPC","type":"exact"},{"name":"peritoneal serous papillary adenocarcinoma","type":"exact"},{"name":"primary peritoneal serous papillary adenocarcinoma","type":"exact"},{"name":"primary peritoneal serous papillary carcinoma","type":"exact"},{"name":"primary serous papillary carcinoma of peritoneum","type":"exact"}],"termid":"MONDO:0018368","xrefs":{"Monarch":{"xref_id":"0018368"}}}


id: PBO:0029504
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_vegetative_cell_population_after_spore_germination,_elongated_germ_tubes_(obsolete_FYPO:0002211)","termid":"PBO:0029504"}


id: PBO:0054913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2327","termid":"PBO:0054913"}


id: MONDO:0015337
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A craniosynostosis that is not part of a larger syndrome.","definition_xrefs":["MONDO:patterns/isolated"],"direct_ancestors":[{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"}],"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":"isolated craniosynostosis","secondary_identifiers":["NANDO:2200843","MEDGEN:1863457","Orphanet:139390","UMLS:C5848302"],"synonyms":[{"name":"nonsyndromic craniosynostosis","type":"exact"}],"termid":"MONDO:0015337","xrefs":{"Monarch":{"xref_id":"0015337"}}}


id: PBO:0027589
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_duration_of_protein_tyrosine_phosphorylation_during_cellular_response_to_salt_stress","termid":"PBO:0027589"}


id: PBO:0079690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin like 4A","termid":"PBO:0079690"}


id: MONDO:0012492
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":"restless legs syndrome, susceptibility to","termid":"MONDO:0100170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restless legs syndrome, susceptibility to, 3","secondary_identifiers":["MEDGEN:355315","OMIM:610438","UMLS:C1864875"],"synonyms":[{"name":"RLS3","type":"exact"},{"name":"restless legs syndrome 3","type":"exact"},{"name":"restless legs syndrome, susceptibility to, 3","type":"exact"}],"termid":"MONDO:0012492","xrefs":{"Monarch":{"xref_id":"0012492"}}}


id: PBO:0056483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrin 3","termid":"PBO:0056483"}


id: PBO:0060970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear transcription factor Y subunit beta","termid":"PBO:0060970"}


id: PBO:0055749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lncRNA negative regulator of antiviral signaling","termid":"PBO:0055749"}


id: MONDO:0010566
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked cone-rod dystrophy","termid":"MONDO:0021155"},{"relation_name":"is_a","term_name":"RPGR-related retinopathy","termid":"MONDO:0100437"}],"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":"X-linked cone-rod dystrophy 1","secondary_identifiers":["UMLS:C1844776","DOID:0111008","MEDGEN:336777","OMIM:304020","GARD:10652","MESH:C564438"],"synonyms":[{"name":"COD1","type":"exact"},{"name":"CORDX1","type":"exact"},{"name":"X-linked cone dystrophy 1","type":"exact"},{"name":"X-linked cone-rod dystrophy type 1","type":"exact"},{"name":"cone dystrophy 1, X-linked","type":"related"},{"name":"cone dystrophy X-linked 1","type":"related"},{"name":"cone-rod dystrophy X-linked 1","type":"related"},{"name":"cone-rod dystrophy, X-linked, 1","type":"related"},{"name":"cone-rod dystrophy, X-linked, 1, X-linked recessive","type":"exact"},{"name":"cone-rod dystrophy, X-linked, type 1","type":"exact"}],"termid":"MONDO:0010566","xrefs":{"Monarch":{"xref_id":"0010566"}}}


id: GO:0003687
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA replication factor (obsolete GO:0003687)","synonyms":[{"name":"DNA replication factor","type":"exact"}],"termid":"GO:0003687"}


id: GO:0140541
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cellular synthesis of Piwi-interacting RNA piRNAs, a class of 24- to 30-nucleotide RNA derived from repeat or complex DNA sequence elements and processed by a Dicer-independent mechanism.","definition_xrefs":["PMID:28847004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription","termid":"GO:0006351"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0006351","GO:0010467"],"is_obsolete":false,"name":"piRNA transcription","synonyms":[{"name":"PIWI-interacting RNA transcription","type":"exact"},{"name":"Piwi-associated RNA transcription","type":"exact"}],"termid":"GO:0140541"}


id: GO:0048201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which vesicles formed at the plasma membrane are directed to specific destinations in endosome membranes, mediated by molecules at the vesicle membrane and target membrane surfaces.","definition_xrefs":["GOC:mah","ISBN:0716731363","PMID:10219233","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle targeting","termid":"GO:0006903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"vesicle targeting, plasma membrane to endosome","synonyms":[{"name":"plasma membrane to endosome targeting","type":"exact"}],"termid":"GO:0048201"}


id: MONDO:0012046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"otosclerosis","termid":"MONDO:0005349"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital corneal opacities, cornea guttata, and corectopia","secondary_identifiers":["MESH:C563921","OMIM:608484","UMLS:C1837970","MEDGEN:324911"],"synonyms":[{"name":"congenital corneal opacities, cornea guttata, and corectopia","type":"exact"},{"name":"corneal opacities, congenital, with cornea guttata and corectopia","type":"related"}],"termid":"MONDO:0012046","xrefs":{"Monarch":{"xref_id":"0012046"}}}


id: GO:0014835
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized satellite cell acquires specialized features of a myoblast. This occurs as part of skeletal muscle regeneration. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["GOC:ef","CL:0000056","PMID:16607119","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myoblast differentiation","termid":"GO:0045445"},{"relation_name":"part_of","term_name":"skeletal muscle tissue regeneration","termid":"GO:0043403"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"myoblast differentiation involved in skeletal muscle regeneration","termid":"GO:0014835"}


id: PBO:0038275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase allele types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino_acid_insertion_and_mutation","termid":"PBO:0038275"}


id: MONDO:0016200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase (obsolete MONDO:0016200)","secondary_identifiers":["Orphanet:209203"],"synonyms":[{"name":"qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase type -","type":"exact"}],"termid":"MONDO:0016200","xrefs":{"Monarch":{"xref_id":"0016200"}}}


id: SO:0005853
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that can be substituted for a related gene at a different site in the genome.","definition_xrefs":["SGD:se"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene_cassette","secondary_identifiers":["http://en.wikipedia.org/wiki/Gene_cassette"],"synonyms":[{"name":"gene cassette","type":"exact"}],"termid":"SO:0005853"}


id: GO:0018137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a peptidyl cysteine-peptidyl glycine cross-link by the condensation of a cysteine thiol with the carbonyl of the preceding residue and alpha-beta dehydrogenation.","definition_xrefs":["RESID:AA0241"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via glycine thiazolecarboxylic acid (obsolete GO:0018137)","termid":"GO:0018137"}


id: GO:0001744
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Establishment of the optic lobe placode. In Drosophila, for example, the placode appears in the dorsolateral region of the head in late stage 11 embryos and is the precursor to the larval visual system.","definition_xrefs":["GOC:mtg_sensu","PMID:8402833"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal placode formation","termid":"GO:0060788"},{"relation_name":"part_of","term_name":"insect visual primordium development","termid":"GO:0001748"}],"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":"insect visual primordium formation","secondary_identifiers":["GO:0007457"],"synonyms":[{"name":"optic lobe and Bolwig's organ precursor formation","type":"exact"},{"name":"optic lobe placode formation","type":"exact"}],"termid":"GO:0001744"}


id: GO:0061057
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by binding of peptidoglycan to a receptor and ending with regulation of a downstream cellular process. The main outcome of the Imd signaling is the production of antimicrobial peptides.","definition_xrefs":["PMID:24706930","PMID:18688280","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern recognition receptor signaling pathway","termid":"GO:0002221"},{"relation_name":"part_of","term_name":"defense response to bacterium","termid":"GO:0042742"}],"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":"peptidoglycan recognition protein signaling pathway","synonyms":[{"name":"Imd signaling pathway","type":"exact"},{"name":"Imd signalling pathway","type":"exact"},{"name":"PGRP signaling pathway","type":"related"},{"name":"immune deficiency pathway","type":"related"},{"name":"immune deficiency signaling pathway","type":"related"}],"termid":"GO:0061057"}


id: GO:0010482
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the physical partitioning and separation of an epidermal cell into daughter cells. An epidermal cell is any of the cells that make up the epidermis.","definition_xrefs":["PMID:17450124"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell division","termid":"GO:0051302"},{"relation_name":"regulates","term_name":"epidermal cell division","termid":"GO:0010481"}],"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 epidermal cell division","synonyms":[{"name":"regulation of hypodermal cell division","type":"related"}],"termid":"GO:0010482"}


id: PBO:0044240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cupin superfamily member 1, pseudogene","termid":"PBO:0044240"}


id: PBO:0090996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Atg8-interacting ER-phagy receptor Epr1","termid":"PBO:0090996"}


id: GO:0018161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dipyrrins (pyrromethanes), compounds containing two pyrrole rings linked through a methine, -CH=, group.","definition_xrefs":["PMID:17430001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"dipyrrin metabolic process","termid":"GO:0046453"}],"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":"dipyrrin biosynthetic process","synonyms":[{"name":"dipyrrin anabolism","type":"exact"},{"name":"dipyrrin biosynthesis","type":"exact"},{"name":"dipyrrin formation","type":"exact"},{"name":"dipyrrin synthesis","type":"exact"},{"name":"dipyrromethane biosynthesis","type":"exact"},{"name":"dipyrromethane biosynthetic process","type":"exact"}],"termid":"GO:0018161"}


id: PBO:0085658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in mRNA export; component of the transcription export (TREX) complex","termid":"PBO:0085658"}


id: PBO:0018125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malate dehydrogenase Mdh1 (predicted)","termid":"PBO:0018125"}


id: SO:0001060
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence_variant is a non exact copy of a sequence_feature or genome exhibiting one or more sequence_alteration.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence_variant","synonyms":[{"name":"ANNOVAR:unknown","type":"related"},{"name":"Jannovar:sequence_variant","type":"exact"},{"name":"VAAST:sequence_variant","type":"exact"},{"name":"sequence variant","type":"exact"}],"termid":"SO:0001060"}


id: MONDO:0004850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete yellow fever (obsolete MONDO:0004850)","termid":"MONDO:0004850","xrefs":{"Monarch":{"xref_id":"0004850"}}}


id: PBO:0060236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYB proto-oncogene like 1","termid":"PBO:0060236"}


id: GO:0140907
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: R-CH + a halogen + FADH2 + O2 = R-C-halogen + FAD + H2O.","definition_xrefs":["PMID:34368824","PMID:28466644"],"direct_ancestors":[{"relation_name":"is_a","term_name":"halogenase activity","termid":"GO:0140906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"flavin-dependent halogenase activity","termid":"GO:0140907"}


id: MONDO:1012294
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"polymicrogyria and asymmetrical ventricular dilation, non-human animal","termid":"MONDO:1011864"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polymicrogyria and asymmetrical ventricular dilation, dog","secondary_identifiers":["OMIA:001098-9615"],"termid":"MONDO:1012294","xrefs":{"Monarch":{"xref_id":"1012294"}}}


id: GO:0006369
data:
  {"annotated_genes":["SJAG_03179","SJAG_02156","SJAG_03923","SJAG_04006","SJAG_04527","SJAG_02037","SJAG_04942","SJAG_03624","SJAG_01713","SJAG_03689","SJAG_03126","SJAG_02242"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[57553,61588,76077,76165,81146,109671,118010],"is_not":false,"summary":null,"term":"GO:0006369"},{"annotations":[113968],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1904595"},{"annotations":[99171,61944,109439,66363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030847"}]},"cv_name":"biological_process","definition":"A transcription termination process that completes the production of a primary RNA polymerase II transcript.","definition_xrefs":["GOC:mah","GOC:txnOH","PMID:27371117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription termination","termid":"GO:0006353"},{"relation_name":"part_of","term_name":"transcription by RNA polymerase II","termid":"GO:0006366"}],"gene_count":12,"genes_by_uniquename":{"SJAG_01713":null,"SJAG_02037":null,"SJAG_02156":null,"SJAG_02242":null,"SJAG_03126":null,"SJAG_03179":null,"SJAG_03624":null,"SJAG_03689":null,"SJAG_03923":null,"SJAG_04006":null,"SJAG_04527":null,"SJAG_04942":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006351"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006351","GO:0010467"],"is_obsolete":false,"name":"termination of RNA polymerase II transcription","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0019224","Reactome:R-HSA-73856"],"synonyms":[{"name":"RNA 3'-end formation by RNA polymerase II","type":"exact"},{"name":"RNA polymerase II transcription termination","type":"exact"},{"name":"RNA polymerase II transcription termination factor activity","type":"related"},{"name":"transcription termination from Pol II promoter","type":"exact"},{"name":"transcription termination from RNA polymerase II promoter","type":"exact"}],"termid":"GO:0006369","terms_by_termid":{"GO:0006369":null,"GO:0030847":null,"GO:1904595":null}}


id: _global:indirectly_causally_upstream_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"p is indirectly causally upstream of q iff p is causally upstream of q and there exists some process r such that p is causally upstream of r and r is causally upstream of q.","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_upstream_of","termid":"_global:causally_upstream_of"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"indirectly_causally_upstream_of","secondary_identifiers":["RO:0012011"],"termid":"_global:indirectly_causally_upstream_of"}


id: PBO:0086769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; similar to transcriptional regulators from the Zn[2]-Cys[6] binuclear cluster protein family; mRNA is weakly cell cycle regulated, peaking in S phase; induced rapidly upon MMS treatment","termid":"PBO:0086769"}


id: MONDO:0001450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete arachnoiditis (obsolete MONDO:0001450)","termid":"MONDO:0001450","xrefs":{"Monarch":{"xref_id":"0001450"}}}


id: PBO:0057803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3125","termid":"PBO:0057803"}


id: GO:0090404
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region at growing end of the pollen tube cell, where polarized growth occurs.","definition_xrefs":["PO:0025281","PO:0025195","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growing cell tip","termid":"GO:0035838"},{"relation_name":"part_of","term_name":"pollen tube","termid":"GO:0090406"}],"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":"pollen tube tip","termid":"GO:0090404"}


id: PBO:0089919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol phoshorylceramide synthase regulatory subunit Kei1","termid":"PBO:0089919"}


id: PBO:0085230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Part of the heteromeric co-chaperone GimC/prefoldin complex; complex promotes efficient protein folding","termid":"PBO:0085230"}


id: SO:0000522
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one V-gene, one VDJ-gene and one J-gene.","direct_ancestors":[{"relation_name":"has_part","term_name":"V_gene_segment","termid":"SO:0000466"},{"relation_name":"has_part","term_name":"J_gene_segment","termid":"SO:0000470"},{"relation_name":"has_part","term_name":"VDJ_gene_segment","termid":"SO:0000574"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_gene_cluster","termid":"SO:0000938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V_VDJ_J_cluster","synonyms":[{"name":"V VDJ J cluster","type":"exact"},{"name":"V-(VDJ)-J-CLUSTER","type":"related"}],"termid":"SO:0000522"}


id: GO:0009867
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by jasmonic acid.","definition_xrefs":["PMID:19522558","GOC:jy","PMID:16478936","PMID:20159850"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone-mediated signaling pathway","termid":"GO:0009755"},{"relation_name":"part_of","term_name":"cellular response to jasmonic acid stimulus","termid":"GO:0071395"}],"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":"jasmonic acid mediated signaling pathway","synonyms":[{"name":"JA signaling","type":"exact"},{"name":"jasmonate signaling","type":"related"},{"name":"jasmonic acid mediated signalling pathway","type":"exact"}],"termid":"GO:0009867"}


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


id: MONDO:0060777
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually solitary polypoid lesion that arises from the cervix. It usually affects women in their reproductive years. It is characterized by the presence of a connective tissue core and overlying epithelium.","definition_xrefs":["NCIT:C40200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical polyp","termid":"MONDO:0000751"},{"relation_name":"is_a","term_name":"fibroepithelial polyp","termid":"MONDO:0060765"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical fibroepithelial polyp","secondary_identifiers":["UMLS:C1516413","MEDGEN:308945"],"synonyms":[{"name":"Cervical fibroepithelial polyp","type":"exact"},{"name":"uterine cervix fibroepithelial polyp","type":"exact"}],"termid":"MONDO:0060777","xrefs":{"Monarch":{"xref_id":"0060777"}}}


id: GO:0140853
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cholesterol + glycyl-L-cysteinyl-[protein] + H+ = [protein]-C-terminal glycyl cholesterol ester + N-terminal L-cysteinyl-[protein].","definition_xrefs":["PMID:8824192","RHEA:59504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity","termid":"GO:0016740"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"cholesterol-protein transferase activity","synonyms":[{"name":"cholesterol transferase activity","type":"broad"}],"termid":"GO:0140853"}


id: GO:0042581
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Granule with a membranous, tubular internal structure, found primarily in mature neutrophil cells. Most are released into the extracellular fluid. Specific granules contain lactoferrin, lysozyme, vitamin B12 binding protein and elastase.","definition_xrefs":["ISBN:0721662544","PMID:7334549","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule","termid":"GO:0030141"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"specific granule","secondary_identifiers":["Wikipedia:Specific_granule"],"synonyms":[{"name":"secondary granule","type":"exact"}],"termid":"GO:0042581"}


id: PBO:0091738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAR adaptor protein, human endophilin A1-like ortholog, implicated in endocytosis","termid":"PBO:0091738"}


id: MONDO:0010746
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":"thumbs, congenital Clasped","secondary_identifiers":["UMLS:C0431886","MEDGEN:98140","OMIM:314100"],"synonyms":[{"name":"Clasped thumbs, congenital","type":"related"},{"name":"adducted thumbs syndrome","type":"related"},{"name":"thumbs, congenital Clasped","type":"exact"}],"termid":"MONDO:0010746","xrefs":{"Monarch":{"xref_id":"0010746"}}}


id: MONDO:0001922
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An abscess that is located in the ureter.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ureteral disorder","termid":"MONDO:0001926"},{"relation_name":"is_a","term_name":"abscess","termid":"MONDO:0005227"},{"relation_name":"is_a","term_name":"urinary tract infection","termid":"MONDO:0100338"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyoureter","secondary_identifiers":["MEDGEN:19600","UMLS:C0034223","DOID:1425","NCIT:C35666","ICD9:593.89","icd11.foundation:692694709","SCTID:85884009"],"synonyms":[{"name":"ureter abscess","type":"exact"}],"termid":"MONDO:0001922","xrefs":{"Monarch":{"xref_id":"0001922"}}}


id: PBO:0073321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine incorporator 4","termid":"PBO:0073321"}


id: FYPO:0003766
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which mitochondrial DNA molecules are interlinked by unresolved recombination junctions.","definition_xrefs":["PMID:10954073","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromosome morphology during vegetative growth","termid":"FYPO:0000848"}],"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:0000661"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0001985","FYPO:0001320","FYPO:0000641","FYPO:0000652","FYPO:0005447","FYPO:0000002","FYPO:0000654"],"is_obsolete":false,"name":"aggregated mtDNA","synonyms":[{"name":"aggregated mitochondrial DNA","type":"exact"},{"name":"aggregated mitochondrial chromosomes","type":"exact"},{"name":"aggregated mtDNA during mitotic cell cycle","type":"related"},{"name":"aggregated mtDNA during vegetative growth","type":"exact"},{"name":"fused mitochondrial chromosomes","type":"related"},{"name":"fused mtDNA","type":"related"},{"name":"interlinked mtDNA","type":"exact"}],"termid":"FYPO:0003766"}


id: GO:0043727
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 5-aminoimidazole + CO2 = 5-amino-4-imidazole carboxylate.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete 5-amino-4-imidazole carboxylate lyase activity (obsolete GO:0043727)","termid":"GO:0043727"}


id: PR:Q9UTF6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cytochrome c oxidase subunit 5A, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01180","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":"cytochrome c oxidase subunit 6, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B2.04","secondary_identifiers":["UniProtKB:Q9UTF6"],"synonyms":[{"name":"Spom972h-COX5A","type":"exact"},{"name":"cytochrome c oxidase polypeptide VI (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTF6"}


id: GO:0030152
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a bacteriocin, any of a heterogeneous group of polypeptide antibiotics that are secreted by certain bacterial strains and are able to kill cells of other susceptible (frequently related) strains after adsorption at specific receptors on the cell surface. They include the colicins, and their mechanisms of action vary.","definition_xrefs":["ISBN:0198506732","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxin biosynthetic process","termid":"GO:0009403"},{"relation_name":"is_a","term_name":"peptide antibiotic biosynthetic process","termid":"GO:0030651"},{"relation_name":"is_a","term_name":"bacteriocin metabolic process","termid":"GO:0046224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"bacteriocin biosynthetic process","synonyms":[{"name":"bacteriocin anabolism","type":"exact"},{"name":"bacteriocin biosynthesis","type":"exact"},{"name":"bacteriocin formation","type":"exact"},{"name":"bacteriocin synthesis","type":"exact"}],"termid":"GO:0030152"}


id: GO:0045662
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of myoblast differentiation. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["CL:0000056","GOC:go_curators","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"is_a","term_name":"regulation of myoblast differentiation","termid":"GO:0045661"},{"relation_name":"negatively_regulates","term_name":"myoblast differentiation","termid":"GO:0045445"}],"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 myoblast differentiation","synonyms":[{"name":"down regulation of myoblast differentiation","type":"exact"},{"name":"down-regulation of myoblast differentiation","type":"exact"},{"name":"downregulation of myoblast differentiation","type":"exact"},{"name":"inhibition of myoblast differentiation","type":"narrow"}],"termid":"GO:0045662"}


id: GO:0043006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals that leads to the upregulation of calcium-dependent phospholipase A2 activity in response to the signal.","definition_xrefs":["GOC:jl","GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of phospholipase A2 activity by calcium-mediated signaling (obsolete GO:0043006)","synonyms":[{"name":"activation of phospholipase A2 activity by calcium-mediated signalling","type":"exact"},{"name":"calcium-dependent activation of phospholipase A2","type":"exact"},{"name":"calcium-dependent phospholipase A2 activation","type":"exact"}],"termid":"GO:0043006"}


id: PBO:0044884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENND10 pseudogene 1","termid":"PBO:0044884"}


id: PBO:0076842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TERF2 interacting protein","termid":"PBO:0076842"}


id: PBO:0084664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial 5'-3' exonuclease and sliding exonuclease; required for mitochondrial genome maintenance; distantly related to the RecB nuclease domain of bacterial RecBCD recombinases; may be regulated by the transcription factor Ace2","termid":"PBO:0084664"}


id: GO:0044007
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The movement of an organism from a host to another host or from a host to another place in the environment. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:cc"],"gene_count":0,"genotype_count":0,"name":"obsolete dissemination or transmission of symbiont from host (obsolete GO:0044007)","synonyms":[{"name":"dissemination or transmission of organism from host","type":"exact"}],"termid":"GO:0044007"}


id: PBO:0041312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 66","termid":"PBO:0041312"}


id: PBO:0108973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ciliary microtubule inner protein 4","termid":"PBO:0108973"}


id: MONDO:1010211
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mycosis fungoides that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-hodgkin lymphoma, non-human animal","termid":"MONDO:1010214"},{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"},{"relation_name":"is_a","term_name":"cancer, non-human animal","termid":"MONDO:1011828"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mycosis fungoides, non-human animal","secondary_identifiers":["OMIA:001109"],"termid":"MONDO:1010211","xrefs":{"Monarch":{"xref_id":"1010211"}}}


id: MONDO:0036511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that affects the kidney and occurs in childhood.","definition_xrefs":["NCIT:C123907"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney cancer","termid":"MONDO:0002367"},{"relation_name":"is_a","term_name":"childhood kidney neoplasm","termid":"MONDO:0002730"},{"relation_name":"is_a","term_name":"childhood malignant neoplasm","termid":"MONDO:0006517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"childhood malignant kidney neoplasm","secondary_identifiers":["MEDGEN:904186","UMLS:C4086162"],"synonyms":[{"name":"childhood kidney cancer","type":"exact"},{"name":"childhood malignant kidney neoplasm","type":"exact"},{"name":"childhood malignant kidney tumor","type":"exact"},{"name":"childhood malignant kidney tumour","type":"exact"},{"name":"childhood malignant renal neoplasm","type":"exact"},{"name":"childhood malignant renal tumor","type":"exact"},{"name":"childhood malignant renal tumour","type":"exact"},{"name":"kidney cancer of childhood","type":"exact"},{"name":"paediatric kidney cancer","type":"exact"},{"name":"pediatric kidney cancer","type":"exact"}],"termid":"MONDO:0036511","xrefs":{"Monarch":{"xref_id":"0036511"}}}


id: FYPO:0006306
data:
  {"alleles_by_uniquename":{"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_03596:allele-1":{"allele_type":"amino_acid_mutation","description":"L264P,P442T","gene_uniquename":"SJAG_03596","name":"cdc15-A","uniquename":"SJAG_03596:allele-1"},"SJAG_04280:allele-2":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-2"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"},"SJAG_04703:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04703","name":"for3delta","uniquename":"SJAG_04703:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000231"},{"annotations":[121282],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[121678],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"}],"single_locus_phenotype":[{"annotations":[121270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000231"},{"annotations":[121682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000198"},{"annotations":[121205,121220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002998"},{"annotations":[121658],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0003315"},{"annotations":[121303],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0002026"},{"annotations":[121547,121271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[121679],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which an actin filament-based process, i.e. any process that depends upon or alters the actin cytoskeleton, is abnormal.","definition_xrefs":["GO:0030029","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":7,"genes_by_uniquename":{"SJAG_01143":null,"SJAG_02392":null,"SJAG_02592":null,"SJAG_03596":null,"SJAG_04280":null,"SJAG_04522":null,"SJAG_04703":null},"genotype_count":10,"genotypes_by_uniquename":{"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cdc15-A(L264P,P442T aa)","display_uniquename":"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03596:allele-1","expression":"Not assayed or wild type"}]}]},"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta":{"display_name":"cdc15-A(L264P,P442T aa) mid1delta","display_uniquename":"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03596:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"for3delta":{"display_name":"for3delta","display_uniquename":"for3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04703:allele-1","expression":"Null"}]}]},"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]},"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"wee1-as8(T582G aa)","display_uniquename":"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04280","SJAG_04522","SJAG_03596","SJAG_01143","SJAG_02392"],"name":"abnormal actin filament-based process","references_by_uniquename":{"PMID:25866389":null,"PMID:27059155":null,"PMID:30664646":null,"PMID:30726171":null,"PMID:32915139":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_04522","SJAG_03596","SJAG_04280","SJAG_04703","SJAG_01143","SJAG_02392","SJAG_02592"],"single_locus_genotype_uniquenames":["pom1delta","rga4delta","mid1delta","cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type","wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","for3delta","sty1delta"],"synonyms":[{"name":"abnormal actin filament-based process during mitotic cell cycle","type":"related"},{"name":"abnormal actin filament-based process during vegetative growth","type":"exact"},{"name":"abnormal microfilament-based process","type":"related"}],"termid":"FYPO:0006306","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000248":null,"FYECO:0000338":null,"FYPO:0000198":null,"FYPO:0000231":null,"FYPO:0000729":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO:0002998":null,"FYPO:0003315":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:0071252
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 sulfur dioxide (SO2) stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to sulfur dioxide","termid":"GO:0010477"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to sulfur dioxide","termid":"GO:0071252"}


id: PBO:0089784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shuttle craft like transcriptional repressor/ubiquitin-protein ligase E3","termid":"PBO:0089784"}


id: PBO:0079738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBX domain protein 4","termid":"PBO:0079738"}


id: PBO:0091349
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rec12 is released from double-strand breaks covalently bound to oligonucleotides 17-27 nt long","termid":"PBO:0091349"}


id: PBO:0091949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf element Wtf12 (truncated)","termid":"PBO:0091949"}


id: GO:0032836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the glomerular basement membrane over time, from its formation to the mature structure. The glomerular basement membrane is the basal laminal portion of the glomerulus which performs the actual filtration.","definition_xrefs":["GOC:sr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix organization","termid":"GO:0030198"},{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"glomerulus development","termid":"GO:0032835"}],"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":"glomerular basement membrane development","termid":"GO:0032836"}


id: GO:0102854
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-18:2-2-18:1-phosphatidylcholine + O2 + a reduced electron acceptor = 1-18:3-2-18:1-phosphatidylcholine + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-18:2-2-18:1-phosphatidylcholine desaturase activity (obsolete GO:0102854)","termid":"GO:0102854"}


id: GO:0071979
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell motility in which contractile cytoskeletal elements alter cell shape, resulting in the smooth movement of a cell through a liquid medium.","definition_xrefs":["PMID:18461074"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell swimming","termid":"GO:0071975"}],"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":"cytoskeleton-mediated cell swimming","synonyms":[{"name":"cytoskeleton-mediated swimming motility","type":"exact"}],"termid":"GO:0071979"}


id: PBO:0029965
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_cell_cycle_regulation_during_cellular_response_to_hydroxyurea","termid":"PBO:0029965"}


id: MONDO:0016185
data:
  {"annotated_genes":["SJAG_04053","SJAG_04316"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88512,88511],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan","termid":"MONDO:0016155"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04053":null,"SJAG_04316":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322","MONDO:0002320"],"is_obsolete":false,"name":"qualitative or quantitative defects of protein O-mannosyltransferase 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5680852","MEDGEN:1842845","GARD:20424","Orphanet:209033"],"synonyms":[{"name":"qualitative or quantitative defects of protein O-mannosyltransferase type 2","type":"exact"}],"termid":"MONDO:0016185","terms_by_termid":{"MONDO:0013162":null},"xrefs":{"Monarch":{"xref_id":"0016185"}}}


id: PBO:0000558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron responsive transcriptional regulator, peptidase family (predicted)","termid":"PBO:0000558"}


id: MOD:00470
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:92"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NHS-LC-Biotin","synonyms":[{"name":"NHS-LC-Biotin","type":"related"}],"termid":"MOD:00470"}


id: PBO:0035977
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_acetylation_during_vegetative_growth","termid":"PBO:0035977"}


id: PBO:0031675
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_spindle_pole_body_localization","termid":"PBO:0031675"}


id: PBO:0001835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cAMP-independent regulatory protein Pac2","termid":"PBO:0001835"}


id: PBO:0028306
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_phosphorylation_during_mitotic_S_phase","termid":"PBO:0028306"}


id: PR:O94460
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A queuine tRNA-ribosyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00369","PANTHER:PTHR11962:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"queuine tRNA-ribosyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.19c","secondary_identifiers":["UniProtKB:O94460"],"synonyms":[{"name":"Spom972h-QTRT1","type":"exact"},{"name":"guanine insertion enzyme (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tRNA-guanine transglycosylase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94460"}


id: PBO:0090732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQGAP domain cytoskeleton scaffold protein Rng2","termid":"PBO:0090732"}


id: FYPO:0000382
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the rate, or speed, of macroautophagy is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal macroautophagy","termid":"FYPO:0000163"}],"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"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased rate of macroautophagy","synonyms":[{"name":"autophagy: decreased rate","type":"broad"},{"name":"decreased rate of autophagy","type":"broad"},{"name":"reduced rate of macroautophagy","type":"exact"}],"termid":"FYPO:0000382"}


id: GO:0008351
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 microtubule severing activity (obsolete GO:0008351)","synonyms":[{"name":"microtubule severing activity","type":"exact"}],"termid":"GO:0008351"}


id: PBO:0086319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with similarity to GPI-anchored aspartic proteases; such proteases are Yap1p and Yap3p; mCherry fusion protein localizes to the vacuole","termid":"PBO:0086319"}


id: PATO:0002442
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A surface feature shape in which the bearer's surface is lacking ridges, pits, rugosity or other surface structures.","definition_xrefs":["PATOC:AD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ornamentation","termid":"PATO:0002440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unornamented","termid":"PATO:0002442"}


id: PBO:0002532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESCRT III complex subunit Vps24","termid":"PBO:0002532"}


id: FYPO:0003948
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of sulfite reductase 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:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0000654","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"abnormal sulfite reductase activity","synonyms":[{"name":"abnormal sulphite reductase activity","type":"exact"}],"termid":"FYPO:0003948"}


id: PBO:0060012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 32","termid":"PBO:0060012"}


id: GO:2000244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of FtsZ-dependent cytokinesis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokinesis","termid":"GO:0032465"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"FtsZ-dependent cytokinesis","termid":"GO:0043093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of FtsZ-dependent cytokinesis","synonyms":[{"name":"regulation of prokaryote-type cytokinesis","type":"related"},{"name":"regulation of prokaryotic fission","type":"related"}],"termid":"GO:2000244"}


id: PBO:0003009
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteomics data indicates an N terminally extended version of this gene which would contain and upstream stop codon and a frameshift","termid":"PBO:0003009"}


id: PATO:0001748
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality in which a portion of the outermost boundary of an entity folds in space such that a portion that was originally convex is now concave.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"concave","termid":"PATO:0001857"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"invaginated","termid":"PATO:0001748"}


id: FYPO:0004408
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing triplatin tetranitrate (also called BBR 3464).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0000139","FYPO:0002060","FYPO:0000003","FYPO:0000257","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on triplatin tetranitrate","synonyms":[{"name":"normal cell population growth in presence of triplatin tetranitrate","type":"exact"},{"name":"normal cell population growth on BBR 3464","type":"exact"},{"name":"normal cell population growth on triplatin tetranitrate","type":"exact"},{"name":"normal cellular response to triplatin tetranitrate","type":"related"},{"name":"normal vegetative cell population growth on triplatin tetranitrate","type":"exact"}],"termid":"FYPO:0004408"}


id: PBO:0030703
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_Gentian_violet","termid":"PBO:0030703"}


id: FYPO:0003658
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 membrane of any part of the Golgi apparatus is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to Golgi apparatus","termid":"FYPO:0002332"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to Golgi membrane","synonyms":[{"name":"normal protein localisation to Golgi membrane","type":"exact"},{"name":"normal protein localization to Golgi membrane during mitotic cell cycle","type":"related"},{"name":"normal protein localization to Golgi membrane during vegetative growth","type":"exact"}],"termid":"FYPO:0003658"}


id: PBO:0051688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"indolethylamine N-methyltransferase","termid":"PBO:0051688"}


id: GO:0031882
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 5 somatostatin receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatostatin receptor binding","termid":"GO:0031877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"type 5 somatostatin receptor binding","synonyms":[{"name":"type 5 somatostatin receptor ligand","type":"narrow"}],"termid":"GO:0031882"}


id: PBO:0073015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sodium channel epithelial 1 subunit delta","termid":"PBO:0073015"}


id: PBO:0002920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZIP zinc transporter 1 (predicted)","termid":"PBO:0002920"}


id: PBO:0116720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"popeye domain cAMP effector 2","termid":"PBO:0116720"}


id: PBO:0070566
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 32","termid":"PBO:0070566"}


id: PBO:0083745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential component of the Rpd3S histone deacetylase complex; interacts with Eaf3p","termid":"PBO:0083745"}


id: PBO:0059858
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translational initiation factor 2","termid":"PBO:0059858"}


id: GO:0061444
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an endocardial cushion cell over time, from its formation to the mature state.","definition_xrefs":["GOC:dph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac cell development","termid":"GO:0055006"},{"relation_name":"part_of","term_name":"endocardial cushion cell differentiation","termid":"GO:0061443"}],"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":"endocardial cushion cell development","termid":"GO:0061444"}


id: PR:O59805
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC550.07 gene.","definition_xrefs":["UniProtKB:O59805","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":"amidase C550.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC550.07","synonyms":[{"name":"Spom972h-SPCC550.07","type":"exact"}],"termid":"PR:O59805"}


id: GO:0033160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the vectorial transfer of a protein from the cytoplasm into the nucleus, across the nuclear membrane.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of protein import into nucleus, translocation (obsolete GO:0033160)","synonyms":[{"name":"positive regulation of protein import into cell nucleus, translocation","type":"exact"}],"termid":"GO:0033160"}


id: SO:0001626
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant where at least one base of the final codon of an incompletely annotated transcript is changed.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminator_codon_variant","termid":"SO:0001590"},{"relation_name":"is_a","term_name":"inframe_variant","termid":"SO:0001650"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"incomplete_terminal_codon_variant","secondary_identifiers":["http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences"],"synonyms":[{"name":"VEP:incomplete_terminal_codon_variant","type":"exact"},{"name":"incomplete terminal codon variant","type":"exact"},{"name":"partial_codon","type":"exact"}],"termid":"SO:0001626"}


id: PBO:0076181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 6B member 1","termid":"PBO:0076181"}


id: SO:0001054
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A portion of a transposon, interrupted by the insertion of another element.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"repeat_component","termid":"SO:0000840"},{"relation_name":"part_of","term_name":"nested_transposon","termid":"SO:0001648"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transposon_fragment","synonyms":[{"name":"transposon fragment","type":"exact"}],"termid":"SO:0001054"}


id: PBO:0050959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon lambda 2","termid":"PBO:0050959"}


id: MONDO:0005941
data:
  {"annotated_genes":["SJAG_00260","SJAG_01671","SJAG_01895"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[87466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[87675],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"}]},"cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the retroperitoneum. The vast majority of cases are carcinomas, lymphomas, or sarcomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"retroperitoneal neoplasm","termid":"MONDO:0024645"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_01671":null,"SJAG_01895":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"retroperitoneal cancer","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:5875","EFO:0007466","ICD9:158.0","ICD9:158","MEDGEN:57559","MESH:D012186","SCTID:126872008","UMLS:C0153465","NCIT:C3357","NCIT:C3537"],"synonyms":[{"name":"cancer of retroperitoneal space","type":"exact"},{"name":"malignant neoplasm of retroperitoneal space","type":"exact"},{"name":"malignant neoplasm of retroperitoneum","type":"related"},{"name":"malignant neoplasm of retroperitoneum and peritoneum","type":"exact"},{"name":"malignant retroperitoneal cancer","type":"related"},{"name":"malignant retroperitoneal neoplasm","type":"exact"},{"name":"malignant retroperitoneal space neoplasm","type":"exact"},{"name":"malignant tumor of peritoneum and retroperitoneum","type":"exact"},{"name":"malignant tumour of peritoneum and retroperitoneum","type":"exact"},{"name":"neoplasm of retroperitoneum","type":"broad"},{"name":"neoplasm of the retroperitoneum","type":"broad"},{"name":"retroperitoneal neoplasm","type":"broad"},{"name":"retroperitoneal space cancer","type":"exact"},{"name":"tumor of retroperitoneum","type":"broad"},{"name":"tumour of retroperitoneum","type":"broad"}],"termid":"MONDO:0005941","terms_by_termid":{"MONDO:0007273":null,"MONDO:0011121":null,"MONDO:0013602":null},"xrefs":{"Monarch":{"xref_id":"0005941"}}}


id: PR:O74743
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tif452 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74743"],"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 4E-2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1709.18","synonyms":[{"name":"Spom972h-tif452","type":"exact"},{"name":"eIF-4E-2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eIF-4F 25 kDa subunit 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eIF4E-2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"mRNA cap-binding protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74743"}


id: MONDO:0013332
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":"brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability","secondary_identifiers":["MEDGEN:462240","OMIM:613627","UMLS:C3150890","SCTID:719162001"],"synonyms":[{"name":"Tsukahara syndrome","type":"related"},{"name":"brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability","type":"exact"},{"name":"brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation","type":"exact"}],"termid":"MONDO:0013332","xrefs":{"Monarch":{"xref_id":"0013332"}}}


id: _global:regulates_o_results_in_formation_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"This is the combination of the regulates relation with the results_in_formation_of relation.","definition_xrefs":["GOC:mtg_berkeley_2013"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulates_formation_of","secondary_identifiers":["GOREL:0001025"],"termid":"_global:regulates_o_results_in_formation_of"}


id: MONDO:0004608
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm that affects the oropharynx.","definition_xrefs":["NCIT:C7398"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pharynx cancer","termid":"MONDO:0005517"},{"relation_name":"is_a","term_name":"neoplasm of oropharynx","termid":"MONDO:0021364"}],"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:0004335","MONDO:0004992"],"is_obsolete":false,"name":"oropharynx cancer","secondary_identifiers":["DOID:8557","ICD9:146.6","EFO:1001931","ICD9:146.5","ICD9:146.7","ICD9:146","MESH:D009959","MEDGEN:57783","ICD9:146.9","ICD10CM:C10","UMLS:C0153382"],"synonyms":[{"name":"cancer of oropharynx","type":"exact"},{"name":"malignant neoplasm of junctional region of oropharynx","type":"exact"},{"name":"malignant neoplasm of lateral wall of oropharynx","type":"exact"},{"name":"malignant neoplasm of oropharynx","type":"exact"},{"name":"malignant neoplasm of posterior wall of oropharynx","type":"exact"},{"name":"malignant neoplasm of the oropharynx","type":"exact"},{"name":"malignant oropharyngeal neoplasm","type":"exact"},{"name":"malignant oropharyngeal tumor","type":"exact"},{"name":"malignant oropharyngeal tumour","type":"exact"},{"name":"malignant oropharynx neoplasm","type":"exact"},{"name":"malignant tumor of mesopharynx","type":"exact"},{"name":"malignant tumor of oropharynx","type":"exact"},{"name":"malignant tumor of posterior wall of oropharynx","type":"exact"},{"name":"malignant tumor of the oropharynx","type":"exact"},{"name":"malignant tumour of mesopharynx","type":"exact"},{"name":"malignant tumour of oropharynx","type":"exact"},{"name":"malignant tumour of posterior wall of oropharynx","type":"exact"},{"name":"malignant tumour of the oropharynx","type":"exact"},{"name":"oropharyngeal cancer","type":"exact"},{"name":"oropharyngeal carcinoma","type":"narrow"},{"name":"oropharynx cancer","type":"exact"},{"name":"primary malignant neoplasm of lateral wall of oropharynx","type":"exact"}],"termid":"MONDO:0004608","xrefs":{"Monarch":{"xref_id":"0004608"}}}


id: MONDO:0001718
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the sclera.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"scleral disorder","termid":"MONDO:0001269"}],"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":"scleritis","secondary_identifiers":["MESH:D015423","DOID:13452","icd11.foundation:2097802831","ICD9:379.00","NCIT:C119046","MEDGEN:48585","HP:0100532","SCTID:78370002","UMLS:C0036416"],"synonyms":[{"name":"scleritis","type":"exact"},{"name":"scleritis (disease)","type":"exact"}],"termid":"MONDO:0001718","xrefs":{"Monarch":{"xref_id":"0001718"}}}


id: PBO:0070875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15 pseudogene 6","termid":"PBO:0070875"}


id: MONDO:1012627
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any progressive degenerative myeloencephalopathy that occurs in cattle due to a mutation in the PNPLA8 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"degenerative myeloencephalopathy, non-human animal","termid":"MONDO:1011866"},{"relation_name":"is_a","term_name":"hereditary neurological disease, non-human animal","termid":"MONDO:1012972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive degenerative myeloencephalopathy, PNPLA8-related, cattle","secondary_identifiers":["OMIA:000827-9913"],"synonyms":[{"name":"Weaver syndrome, cattle","type":"related"},{"name":"bovine degenerative progressive myeloencephalopathy","type":"related"},{"name":"haplotype BHW, cattle","type":"related"},{"name":"myeloencephalopathy, progressive degenerative, PNPLA8-related, cattle","type":"exact"}],"termid":"MONDO:1012627","xrefs":{"Monarch":{"xref_id":"1012627"}}}


id: GO:0098600
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-Selenomethionine + H2O => Methaneselenol + Ammonia + 2-oxobutanoic acid.","definition_xrefs":["PMID:16444005","PMID:11578145","PMID:16037612"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"selenomethionine gamma-lyase activity","secondary_identifiers":["Reactome:R-HSA-2408537"],"termid":"GO:0098600"}


id: MONDO:0024388
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with bacteria of the genus clostridium.","definition_xrefs":["MESH:D003015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gram-positive bacterial infections","termid":"MONDO:0021679"},{"relation_name":"is_a","term_name":"anaerobic bacteria infectious disease","termid":"MONDO:0024389"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clostridium infectious disease","secondary_identifiers":["ICD9:040.89","SCTID:56688005","EFO:1000874"],"synonyms":[{"name":"Clostridium infection","type":"related"},{"name":"commensal Clostridium infection","type":"related"},{"name":"commensal infection, Clostridium","type":"related"},{"name":"commensal infections, Clostridium","type":"related"},{"name":"infection, Clostridium","type":"related"},{"name":"infections, Clostridium","type":"related"}],"termid":"MONDO:0024388","xrefs":{"Monarch":{"xref_id":"0024388"}}}


id: MONDO:1010758
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acrodermatitis enteropathica that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acrodermatitis enteropathica, non-human animal","termid":"MONDO:1010133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acrodermatitis enteropathica, domestic cat","secondary_identifiers":["OMIA:000593-9685"],"termid":"MONDO:1010758","xrefs":{"Monarch":{"xref_id":"1010758"}}}


id: MONDO:0000068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mucolipidosis (obsolete MONDO:0000068)","termid":"MONDO:0000068","xrefs":{"Monarch":{"xref_id":"0000068"}}}


id: PBO:0057311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 517b","termid":"PBO:0057311"}


id: MONDO:0009346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"histidinemia","termid":"MONDO:0009345"},{"relation_name":"is_a","term_name":"inborn disorder of amino acid transport","termid":"MONDO:0019216"}],"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":"histidinuria due to a renal tubular defect","secondary_identifiers":["MEDGEN:82825","GARD:2708","OMIM:235830","MESH:C538321","Orphanet:2158","UMLS:C0268642"],"synonyms":[{"name":"histidinuria due to a renal tubular defect","type":"exact"},{"name":"histidinuria-renal tubular defect syndrome","type":"exact"}],"termid":"MONDO:0009346","xrefs":{"Monarch":{"xref_id":"0009346"}}}


id: MONDO:0008828
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Camptodactyly-arthropathy-coxa-vara-pericarditis (CACP) syndrome is a rare, genetic, rheumatologic disease characterized by congenital or early-onset camptodactyly and symmetrical, polyarticular, non-inflammatory, large joint arthropathy with synovial hyperplasia, as well as progressive coxa vara deformity and, occasionally, non-inflammatory pericarditis.","definition_xrefs":["Orphanet:2848"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rheumatic disorder","termid":"MONDO:0005554"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"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":"camptodactyly-arthropathy-coxa vara-pericarditis syndrome","secondary_identifiers":["OMIM:208250","DOID:0090127","MESH:C537560","UMLS:C1859690","GARD:306","EFO:0009028","MEDGEN:349226"],"synonyms":[{"name":"CACP","type":"exact"},{"name":"CACP syndrome","type":"exact"},{"name":"Jacobs syndrome","type":"exact"},{"name":"PAC syndrome","type":"exact"},{"name":"arthropathy camptodactyly syndrome","type":"related"},{"name":"arthropathy-camptodactyly syndrome","type":"exact"},{"name":"camptodactyly arthropathy coxa vara pericarditis syndrome","type":"related"},{"name":"camptodactyly arthropathy pericarditis syndrome","type":"related"},{"name":"camptodactyly-arthropathy-coxa vara-pericarditis syndrome","type":"exact"},{"name":"camptodactyly-arthropathy-coxa-vara-pericarditis syndrome","type":"related"},{"name":"camptodactyly-arthropathy-pericarditis syndrome","type":"exact"},{"name":"congenital familial hypertrophic synovitis","type":"exact"},{"name":"familial fibrosing serositis","type":"exact"},{"name":"fibrosing serositis, familial","type":"related"},{"name":"hypertrophic synovitis, congenital familial","type":"related"},{"name":"pericarditis arthropathy camptodactyly syndrome","type":"related"},{"name":"pericarditis-arthropathy-camptodactyly syndrome","type":"exact"}],"termid":"MONDO:0008828","xrefs":{"Monarch":{"xref_id":"0008828"}}}


id: MONDO:0002826
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tuberculosis (obsolete MONDO:0002826)","termid":"MONDO:0002826","xrefs":{"Monarch":{"xref_id":"0002826"}}}


id: MONDO:0011421
data:
  {"annotated_genes":["SJAG_01503"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87329],"is_not":false,"summary":null,"term":"MONDO:0011421"}]},"cv_name":"mondo","definition":"Any mitochondrial proton-transporting ATP synthase complex deficiency in which the cause of the disease is a mutation in the ATPAF2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex deficiency","termid":"MONDO:0000066"},{"relation_name":"is_a","term_name":"mitochondrial proton-transporting ATP synthase complex deficiency","termid":"MONDO:0014471"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01503":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial complex V (ATP synthase) deficiency, nuclear type 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:604273","DOID:0050768","MEDGEN:477906","UMLS:C3276276","GARD:18660"],"synonyms":[{"name":"ATPAF2 mitochondrial proton-transporting ATP synthase complex deficiency","type":"exact"},{"name":"Complex 5 mitochondrial respiratory chain deficiency","type":"related"},{"name":"MC5DN1","type":"exact"},{"name":"mitochondrial Complex 5 (ATP synthase) deficiency, Atpaf2 type","type":"related"},{"name":"mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 1","type":"related"},{"name":"mitochondrial complex V (ATP synthase) deficiency, nuclear type 1","type":"exact"},{"name":"mitochondrial complex V deficiency","type":"broad"},{"name":"mitochondrial proton-transporting ATP synthase complex deficiency caused by mutation in ATPAF2","type":"exact"}],"termid":"MONDO:0011421","terms_by_termid":{"MONDO:0011421":null},"xrefs":{"Monarch":{"xref_id":"0011421"}}}


id: PBO:0017654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stationary phase-specific homeobox transcription factor Phx1","termid":"PBO:0017654"}


id: PBO:0073101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate dehydrogenase complex subunit D pseudogene 5","termid":"PBO:0073101"}


id: PBO:0054263
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 1648","termid":"PBO:0054263"}


id: PBO:0029550
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_cell_at_low_temperature","termid":"PBO:0029550"}


id: PBO:0088029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UbiB family mitochondrial protein; involved in mobilization of CoQ from its site of synthesis on the inner mitochondrial membrane to other sites of action; contains transmembrane domain and mitochondrial targeting sequence","termid":"PBO:0088029"}


id: MONDO:0006703
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete chronic interstitial cystitis (obsolete MONDO:0006703)","termid":"MONDO:0006703","xrefs":{"Monarch":{"xref_id":"0006703"}}}


id: FYPO:0006135
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 citrate 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:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular citrate level","synonyms":[{"name":"increased cellular citrate anion level","type":"exact"},{"name":"increased cellular citrate level during mitotic cell cycle","type":"related"},{"name":"increased cellular citrate level during vegetative growth","type":"exact"},{"name":"increased citrate accumulation","type":"related"}],"termid":"FYPO:0006135"}


id: PBO:0028662
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_replication_slippage_during_replication_fork_processing","termid":"PBO:0028662"}


id: PBO:0040104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arsenite methyltransferase","termid":"PBO:0040104"}


id: PBO:0053586
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 609","termid":"PBO:0053586"}


id: PBO:0049546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B clustered histone 9","termid":"PBO:0049546"}


id: GO:0030835
data:
  {"annotated_genes":["SJAG_00279","SJAG_02700","SJAG_01993","SJAG_01894"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94217,80930,77320,81987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of actin depolymerization.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament depolymerization","termid":"GO:0030834"},{"relation_name":"is_a","term_name":"negative regulation of cytoskeleton organization","termid":"GO:0051494"},{"relation_name":"is_a","term_name":"negative regulation of protein depolymerization","termid":"GO:1901880"},{"relation_name":"is_a","term_name":"negative regulation of supramolecular fiber organization","termid":"GO:1902904"},{"relation_name":"negatively_regulates","term_name":"actin filament depolymerization","termid":"GO:0030042"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00279":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02700":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0030036"],"is_obsolete":false,"name":"negative regulation of actin filament depolymerization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0030044"],"synonyms":[{"name":"actin filament stabilization","type":"exact"},{"name":"down regulation of actin filament depolymerization","type":"exact"},{"name":"down-regulation of actin filament depolymerization","type":"exact"},{"name":"downregulation of actin filament depolymerization","type":"exact"},{"name":"inhibition of actin filament depolymerization","type":"narrow"},{"name":"negative regulation of actin depolymerization","type":"exact"},{"name":"negative regulation of actin polymerization and/or depolymerization","type":"broad"}],"termid":"GO:0030835","terms_by_termid":{"GO:0051016":null}}


id: FYPO:0007783
data:
  {"alleles_by_uniquename":{"SJAG_00028:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00028","name":"rga6delta","uniquename":"SJAG_00028:allele-1"},"SJAG_04280:allele-2":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-2"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121676,121681],"is_not":false,"summary":null,"term":"FYPO:0007783"}],"single_locus_phenotype":[{"annotations":[121677],"is_not":false,"summary":null,"term":"FYPO:0007783"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which cellular geometry scaling, by which cells normally maintain a fairly constant length:diameter (width) ratio upon changes in cell volume, does not occur.","definition_xrefs":["PMID:30664646","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"abnormal vegetative cell morphology","termid":"FYPO:0001118"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00028":null,"SJAG_04280":null,"SJAG_04522":null},"genotype_count":3,"genotypes_by_uniquename":{"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]},"rga6delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga6delta wee1-as8(T582G aa)","display_uniquename":"rga6delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00028:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04280","SJAG_04522","SJAG_00028"],"name":"abolished geometry scaling","references_by_uniquename":{"PMID:30664646":null},"single_locus_annotated_genes":["SJAG_04522"],"single_locus_genotype_uniquenames":["rga4delta"],"synonyms":[{"name":"abolished cell geometry scaling","type":"exact"},{"name":"abolished cellular geometry scaling","type":"exact"},{"name":"abolished geometry scaling during mitotic cell cycle","type":"related"},{"name":"abolished geometry scaling during vegetative growth","type":"exact"},{"name":"geometry scaling abolished","type":"exact"}],"termid":"FYPO:0007783","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000338":null,"FYPO:0007783":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PBO:0030449
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_phosphatase_activity","termid":"PBO:0030449"}


id: PBO:0052078
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 3","termid":"PBO:0052078"}


id: MONDO:0013974
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pure hair and nail ectodermal dysplasia","termid":"MONDO:0019071"}],"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":"ectodermal dysplasia 6, hair/nail type","secondary_identifiers":["OMIM:614928","UMLS:C3554111","DOID:0111659","MEDGEN:767025","GARD:18064"],"synonyms":[{"name":"ECTD6","type":"exact"},{"name":"ectodermal dysplasia 6, hair/nail type","type":"exact"}],"termid":"MONDO:0013974","xrefs":{"Monarch":{"xref_id":"0013974"}}}


id: MONDO:0013831
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 6","secondary_identifiers":["OMIM:614623","UMLS:C3553306","MEDGEN:766220"],"synonyms":[{"name":"KTCN6","type":"exact"},{"name":"keratoconus 6","type":"exact"}],"termid":"MONDO:0013831","xrefs":{"Monarch":{"xref_id":"0013831"}}}


id: MONDO:0018954
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Loeys-Dietz syndrome is a rare genetic connective tissue disorder characterized by a broad spectrum of craniofacial, vascular and skeletal manifestations with four genetic subtypes described forming a clinical continuum.","definition_xrefs":["Orphanet:60030"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"},{"relation_name":"is_a","term_name":"Marfan and Marfan-related disorder","termid":"MONDO:0017310"}],"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":"Loeys-Dietz syndrome","secondary_identifiers":["GARD:10788","ICD9:759.89","MEDGEN:395827","DOID:0050466","NANDO:2200969","OMIMPS:609192","SCTID:446263001","NORD:91173","NCIT:C75006","UMLS:C2697932","MESH:D055947"],"synonyms":[{"name":"Loeys-Dietz syndrome","type":"exact"},{"name":"aortic aneurysm syndrome due to TGF-beta receptors anomalies","type":"exact"},{"name":"aortic aneurysm syndrome, Loeys-Dietz type","type":"related"}],"termid":"MONDO:0018954","xrefs":{"Monarch":{"xref_id":"0018954"}}}


id: PBO:0074975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 114-17","termid":"PBO:0074975"}


id: FYPO:0004721
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which minus-end specific microtubule depolymerization, i.e. the removal of tubulin dimers from the minus end of a microtubule, occurs at a lower rate, or speed, than normal.","definition_xrefs":["GO:0036078","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete decreased rate of microtubule depolymerization at minus end (obsolete FYPO:0004721)","synonyms":[{"name":"decreased microtubule depolymerization rate at minus end","type":"exact"},{"name":"decreased microtubule minus end shrinkage","type":"related"},{"name":"decreased rate of microtubule catastrophe at minus end","type":"related"},{"name":"decreased rate of microtubule depolymerisation at minus end","type":"exact"},{"name":"decreased rate of microtubule depolymerization at minus end during mitotic cell cycle","type":"related"},{"name":"decreased rate of microtubule depolymerization at minus end during vegetative growth","type":"exact"},{"name":"decreased rate of minus-end specific microtubule depolymerization","type":"exact"},{"name":"increased microtubule stability","type":"related"},{"name":"reduced rate of microtubule depolymerization at minus end","type":"exact"}],"termid":"FYPO:0004721"}


id: PBO:0035993
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_methylation_during_vegetative_growth","termid":"PBO:0035993"}


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


id: PBO:0082252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha subunit of the translation initiation factor eIF2; eIF2 is involved in identification of the start codon; phosphorylation of Ser51 is required for regulation of translation by inhibiting the exchange of GDP for GTP; protein abundance increases in response to DNA replication stress","termid":"PBO:0082252"}


id: GO:2000660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of interleukin-1-mediated signaling pathway.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine-mediated signaling pathway","termid":"GO:0001960"},{"relation_name":"is_a","term_name":"regulation of interleukin-1-mediated signaling pathway","termid":"GO:2000659"},{"relation_name":"negatively_regulates","term_name":"interleukin-1-mediated signaling pathway","termid":"GO:0070498"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of interleukin-1-mediated signaling pathway","synonyms":[{"name":"negative regulation of IL-1 alpha-mediated signaling pathway","type":"related"},{"name":"negative regulation of IL-1 beta-mediated signaling pathway","type":"related"},{"name":"negative regulation of IL-1-mediated signaling pathway","type":"exact"},{"name":"negative regulation of interleukin-1 alpha-mediated signaling pathway","type":"related"},{"name":"negative regulation of interleukin-1 beta-mediated signaling pathway","type":"related"},{"name":"negative regulation of interleukin-1-mediated signalling pathway","type":"exact"}],"termid":"GO:2000660"}


id: FYPO:0000361
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of the nucleolus is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"output_of","term_name":"abnormal nucleolus organization","termid":"FYPO:0000814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abnormal nucleolar morphology","synonyms":[{"name":"abnormal nucleolar morphology during mitotic cell cycle","type":"related"},{"name":"abnormal nucleolar morphology during vegetative growth","type":"exact"},{"name":"nucleolar morphology: abnormal","type":"related"}],"termid":"FYPO:0000361"}


id: PBO:0024869
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does not bind rpb1 CTD peptides in vitro","termid":"PBO:0024869"}


id: PBO:0005152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase regulator Vps3 (predicted)","termid":"PBO:0005152"}


id: PBO:0062335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily C member 74","termid":"PBO:0062335"}


id: GO:0022870
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + mannose(out) = protein histidine + mannose phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"},{"relation_name":"is_a","term_name":"mannose transmembrane transporter activity","termid":"GO:0015578"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-mannose phosphotransferase system transporter activity","synonyms":[{"name":"mannose PTS transporter activity","type":"exact"}],"termid":"GO:0022870"}


id: PBO:0044335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 18","termid":"PBO:0044335"}


id: GO:0150116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell-substrate junction organization.","definition_xrefs":["GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"cell-substrate junction organization","termid":"GO:0150115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell-substrate junction organization","termid":"GO:0150116"}


id: PBO:0029400
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_nucleoplasm","termid":"PBO:0029400"}


id: MONDO:0000259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dengue disease","termid":"MONDO:0005502"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asymptomatic dengue","secondary_identifiers":["DOID:0050143"],"termid":"MONDO:0000259","xrefs":{"Monarch":{"xref_id":"0000259"}}}


id: GO:0038068
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the concomitant phosphorylation of threonine (T) and tyrosine (Y) residues in a Thr-Glu-Tyr (TEY) thiolester sequence in a MAP kinase (MAPK) substrate, as part of a MAPK signaling cascade that contributes to cell wall organization or biogenesis.","definition_xrefs":["GOC:signaling"],"gene_count":0,"genotype_count":0,"name":"obsolete MAP kinase kinase activity involved in cell wall organization or biogenesis (obsolete GO:0038068)","synonyms":[{"name":"MAP kinase kinase activity involved in cell wall biogenesis","type":"narrow"},{"name":"MAP2K activity involved in cell wall integrity","type":"exact"},{"name":"MAPKK activity involved in cell wall integrity","type":"exact"}],"termid":"GO:0038068"}


id: GO:1904646
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 amyloid-beta stimulus.","definition_xrefs":["PMID:23555824","GOC:TermGenie","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to amyloid-beta","termid":"GO:1904645"}],"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 amyloid-beta","synonyms":[{"name":"cellular response to beta-amyloid","type":"exact"},{"name":"cellular response to beta-amyloids","type":"related"}],"termid":"GO:1904646"}


id: PBO:0050037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class II, DR beta 5","termid":"PBO:0050037"}


id: GO:0070917
data:
  {"annotated_genes":["SJAG_03015"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78033],"is_not":false,"summary":null,"term":"GO:0070917"}]},"cv_name":"molecular_function","definition":"Binds to and modulates the activity of inositol phosphoceramide synthase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme regulator activity","termid":"GO:0030234"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03015":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0098772","GO:0030234","GO:0003674"],"is_obsolete":false,"name":"inositol phosphoceramide synthase regulator activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"IPC synthase regulator activity","type":"exact"}],"termid":"GO:0070917","terms_by_termid":{"GO:0070917":null}}


id: MONDO:0004528
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A myofibroblastoma arising from the inguinal lymph nodes. It is characterized by the presence of nuclear palisading.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lymph node cancer","termid":"MONDO:0001082"},{"relation_name":"is_a","term_name":"lymph node neoplasm","termid":"MONDO:0024339"},{"relation_name":"is_a","term_name":"myofibroblastoma","termid":"MONDO:0040675"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"lymph node palisaded myofibroblastoma","secondary_identifiers":["DOID:8304","NCIT:C6584","MEDGEN:757257","UMLS:C3164851"],"synonyms":[{"name":"palisaded lymph node myofibroblastoma","type":"exact"},{"name":"palisaded myofibroblastoma of lymph node","type":"exact"},{"name":"palisaded myofibroblastoma of the lymph node","type":"exact"}],"termid":"MONDO:0004528","xrefs":{"Monarch":{"xref_id":"0004528"}}}


id: SO:0000889
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is paternally imprinted.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"paternally_imprinted","termid":"SO:0000136"},{"relation_name":"is_a","term_name":"epigenetically_modified_gene","termid":"SO:0000898"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paternally_imprinted_gene","synonyms":[{"name":"paternally imprinted gene","type":"exact"}],"termid":"SO:0000889"}


id: MONDO:0044321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structural heart defects and renal anomalies syndrome","secondary_identifiers":["OMIM:617478","UMLS:C4479549","MEDGEN:1387412"],"synonyms":[{"name":"SHDRA","type":"related"},{"name":"structural heart defects and renal anomalies syndrome","type":"exact"}],"termid":"MONDO:0044321","xrefs":{"Monarch":{"xref_id":"0044321"}}}


id: PBO:0016117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein Ssa2","termid":"PBO:0016117"}


id: FYPO:0005946
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of one or more cell cycle-regulated mRNAs measured in a cell is lower than normal (i.e. lower than observed in wild-type cells). Cell cycle-regulated mRNAs are transcribed from genes whose level of transcription varies depending on cell cycle phase.","definition_xrefs":["PMID:15195092","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased level of cell cycle regulated gene mRNA during vegetative growth","synonyms":[{"name":"decreased cell cycle regulated gene mRNA accumulation during vegetative growth","type":"related"},{"name":"decreased level of cell cycle regulated gene RNA during vegetative growth","type":"exact"},{"name":"decreased level of cell cycle regulated gene mRNA during mitotic cell cycle","type":"related"},{"name":"decreased level of cell cycle regulated gene transcripts during vegetative growth","type":"exact"},{"name":"decreased level of cell cycle-regulated gene mRNA during vegetative growth","type":"exact"},{"name":"reduced level of cell cycle regulated gene mRNA during vegetative growth","type":"exact"}],"termid":"FYPO:0005946"}


id: PBO:0061197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nitric oxide associated 1","termid":"PBO:0061197"}


id: MOD:01439
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-[2-(pyridin-4-yl)ethyl]-L-cysteine.","definition_xrefs":["PubMed:6528972","PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-pyridylethyl-L-cysteine","termid":"MOD:00424"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-[2-(pyridin-4-yl)ethyl]-L-cysteine","synonyms":[{"name":"4-PEC","type":"exact"},{"name":"Pyridylethyl","type":"related"},{"name":"Pyridylethyl Cystenyl","type":"exact"},{"name":"S-(pyridin-4-ylethyl)-L-cysteine","type":"exact"},{"name":"S-pyridylethylation","type":"related"}],"termid":"MOD:01439"}


id: GO:0097469
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + a protein tyrosine = ADP + protein tyrosine phosphate. This reaction requires the binding of a regulatory cyclin subunit.","definition_xrefs":["PMID:1372994","GOC:vw","GOC:al"],"gene_count":0,"genotype_count":0,"name":"obsolete cyclin-dependent protein tyrosine kinase activity (obsolete GO:0097469)","synonyms":[{"name":"cyclin-dependent protein tyrosine kinase activity","type":"exact"}],"termid":"GO:0097469"}


id: FYPO:0000083
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to enfumafungin. Cells stop growing (and may die) at a concentration of enfumafungin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0001985","FYPO:0000003","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to enfumafungin","synonyms":[{"name":"hypersensitive to enfumafungin","type":"exact"},{"name":"sensitive to enfumafungin during mitotic cell cycle","type":"related"},{"name":"sensitive to enfumafungin during vegetative growth","type":"exact"},{"name":"sensitive to glucan synthase inhibitor","type":"broad"}],"termid":"FYPO:0000083"}


id: PATO:0000783
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000783 digestive function value (obsolete PATO:0000783)","termid":"PATO:0000783"}


id: PBO:0046982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 86 member F, pseudogene","termid":"PBO:0046982"}


id: GO:1900776
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving fumiquinazoline A.","definition_xrefs":["GOC:di","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete fumiquinazoline A metabolic process (obsolete GO:1900776)","synonyms":[{"name":"fumiquinazoline A metabolism","type":"exact"}],"termid":"GO:1900776"}


id: MONDO:0002009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An episode of depression lasting two or more weeks without an intervening episode of mania.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"depressive disorder","termid":"MONDO:0002050"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major depressive disorder","secondary_identifiers":["ICD9:296.30","SCTID:300706003","MEDGEN:266123","OMIM:608516","DOID:1470","SCTID:370143000","UMLS:C1269683","ICD9:296.3","NCIT:C35094","ICD9:296.20","MFOMD:0000143","MESH:D003865","ICD9:296.2","EFO:0003761"],"synonyms":[{"name":"major depression","type":"exact"},{"name":"major depressive disorder","type":"exact"},{"name":"major depressive disorder 1","type":"broad"},{"name":"major depressive disorder 2","type":"broad"},{"name":"major depressive disorder and accelerated response to antidepressant drug treatment","type":"exact"},{"name":"major depressive disorder, response to citalopram therapy in","type":"exact"},{"name":"recurrent major depression","type":"exact"},{"name":"single major depressive episode","type":"exact"},{"name":"unipolar depression","type":"exact"},{"name":"unipolar depression, susceptibility to","type":"exact"}],"termid":"MONDO:0002009","xrefs":{"Monarch":{"xref_id":"0002009"}}}


id: PBO:0001231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"argonaute binding protein 1","termid":"PBO:0001231"}


id: PR:O43086
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- elg1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43086"],"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":"telomere length regulation protein elg1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC947.11c","synonyms":[{"name":"Spom972h-elg1","type":"exact"},{"name":"telomere elongation suppressor elg1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43086"}


id: GO:0102614
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: germacra-1(10),4,11(13)-trien-12-oate + O2 + reduced [NADPH--hemoprotein reductase] = 8beta-hydroxygermacra-1(10),4,11(13)-trien-12-oate + H(+) + H2O + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:57964"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"germacrene A acid 8beta-hydroxylase activity","secondary_identifiers":["EC:1.14.14.168","MetaCyc:RXN-15460"],"termid":"GO:0102614"}


id: PBO:0038779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activin A receptor type 2A","termid":"PBO:0038779"}


id: PR:000044697
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.1, initiator methionine removed K9-methylated form (Schizosaccharomyces pombe) whose methylation type is monomethylation. Example: UniProtKB:P09988-1, 2-136, Lys-10, MOD:00085.","definition_xrefs":["PRO:DAN","PMID:23849629"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hht1/Me(K9)","termid":"PR:000027578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.1, initiator methionine removed K9-monomethylated form (Schizosaccharomyces pombe)","pombase_gene_id":"SPAC1834.04","synonyms":[{"name":"Spom-hht1/InitMet-/K9me1","type":"exact"}],"termid":"PR:000044697"}


id: PBO:0061045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIPA like domain containing 1","termid":"PBO:0061045"}


id: PR:000027571
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3 that is a translation product of the Schizosaccharomyces pombe 972h- hht2 gene or a 1:1 ortholog thereof in fungi.","definition_xrefs":["PMID:11242054","PMID:20929775","PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fungal histone H3.2","pombase_gene_id":"SPBC8D2.04","synonyms":[{"name":"hht2","type":"exact"}],"termid":"PR:000027571"}


id: PBO:0116638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARF guanine nucleotide exchange factor 1","termid":"PBO:0116638"}


id: PBO:0086530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved among S. cerevisiae strains; located in the upstream region of PMA1; deletion leads to polyamine resistance due to downregulation of PMA1","termid":"PBO:0086530"}


id: SO:0001417
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A flanking region located three prime of a specific region.","definition_xrefs":["SO:chado"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flanking_region","termid":"SO:0000239"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_flanking_region","synonyms":[{"name":"3' flanking region","type":"related"},{"name":"three prime flanking region","type":"exact"}],"termid":"SO:0001417"}


id: GO:0000151
data:
  {"annotated_genes":["SJAG_04309","SJAG_03651","SJAG_02044","SJAG_03130","SJAG_03219","SJAG_01068","SJAG_01678","SJAG_02299","SJAG_00666","SJAG_00146","SJAG_04142","SJAG_00439","SJAG_03417","SJAG_02685","SJAG_03809","SJAG_01585","SJAG_02162","SJAG_00071","SJAG_02119","SJAG_03841","SJAG_03575","SJAG_01657","SJAG_02319","SJAG_03561","SJAG_04035","SJAG_05329","SJAG_00341","SJAG_01392","SJAG_03351","SJAG_04574","SJAG_01637","SJAG_03454","SJAG_03350","SJAG_04971","SJAG_05297","SJAG_04087","SJAG_02003","SJAG_03037","SJAG_01480","SJAG_00756","SJAG_01573","SJAG_00651","SJAG_02186","SJAG_03302","SJAG_01886","SJAG_01253","SJAG_02197","SJAG_03385","SJAG_01956","SJAG_00819","SJAG_05012","SJAG_00262","SJAG_04335","SJAG_01051","SJAG_01801","SJAG_03728","SJAG_02041","SJAG_01617","SJAG_05236","SJAG_04540","SJAG_02703","SJAG_03093","SJAG_00656","SJAG_02837","SJAG_03680","SJAG_05274","SJAG_01709","SJAG_02591","SJAG_01022","SJAG_01472","SJAG_01572","SJAG_04619","SJAG_01134","SJAG_03218","SJAG_04520","SJAG_04853","SJAG_01540","SJAG_00552","SJAG_03006","SJAG_02651","SJAG_03345","SJAG_03858","SJAG_00320","SJAG_02822","SJAG_04151","SJAG_04384","SJAG_01533","SJAG_04661","SJAG_00033","SJAG_00435","SJAG_02753","SJAG_00293","SJAG_00192","SJAG_04612","SJAG_00615"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[63690,72367,75342,75935,76050,76149,76996,78731,79245,91216,101562,103418,106551,109198,113033,114991,117668,118775,118872],"is_not":false,"summary":null,"term":"GO:0000151"},{"annotations":[82182,58023,74803,72384,72617,78355,67496,75740,80167,79602,71838,80915,65506,81744,97077,80889,74924,80779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005680"},{"annotations":[98645,120857,96240,119719,115996,112473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043494"},{"annotations":[76685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031463"},{"annotations":[107304,77987,92791,72605,98603,92743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080008"},{"annotations":[71755],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031464"},{"annotations":[81116,99415,77726,81304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035361"},{"annotations":[91125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031461"},{"annotations":[109981,118410,72888,114823,90860,66014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044695"},{"annotations":[72745,79153,81786,90162,82176,116270,80823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034657"},{"annotations":[119184,107261,91134,105916,109646,111556,106778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000836"},{"annotations":[95279,76432,72989,73072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033503"},{"annotations":[112311,106829,92482,99696,96243,111063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043224"},{"annotations":[78905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097505"},{"annotations":[61196,104817,82143,97453,90432,75836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019005"},{"annotations":[93427,111954,98608],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033768"}]},"cv_name":"cellular_component","definition":"A protein complex that includes a ubiquitin-protein ligase and enables ubiquitin protein ligase activity. The complex also contains other proteins that may confer substrate specificity on the complex.","definition_xrefs":["GOC:jh2","PMID:9529603"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"}],"gene_count":95,"genes_by_uniquename":{"SJAG_00033":null,"SJAG_00071":null,"SJAG_00146":null,"SJAG_00192":null,"SJAG_00262":null,"SJAG_00293":null,"SJAG_00320":null,"SJAG_00341":null,"SJAG_00435":null,"SJAG_00439":null,"SJAG_00552":null,"SJAG_00615":null,"SJAG_00651":null,"SJAG_00656":null,"SJAG_00666":null,"SJAG_00756":null,"SJAG_00819":null,"SJAG_01022":null,"SJAG_01051":null,"SJAG_01068":null,"SJAG_01134":null,"SJAG_01253":null,"SJAG_01392":null,"SJAG_01472":null,"SJAG_01480":null,"SJAG_01533":null,"SJAG_01540":null,"SJAG_01572":null,"SJAG_01573":null,"SJAG_01585":null,"SJAG_01617":null,"SJAG_01637":null,"SJAG_01657":null,"SJAG_01678":null,"SJAG_01709":null,"SJAG_01801":null,"SJAG_01886":null,"SJAG_01956":null,"SJAG_02003":null,"SJAG_02041":null,"SJAG_02044":null,"SJAG_02119":null,"SJAG_02162":null,"SJAG_02186":null,"SJAG_02197":null,"SJAG_02299":null,"SJAG_02319":null,"SJAG_02591":null,"SJAG_02651":null,"SJAG_02685":null,"SJAG_02703":null,"SJAG_02753":null,"SJAG_02822":null,"SJAG_02837":null,"SJAG_03006":null,"SJAG_03037":null,"SJAG_03093":null,"SJAG_03130":null,"SJAG_03218":null,"SJAG_03219":null,"SJAG_03302":null,"SJAG_03345":null,"SJAG_03350":null,"SJAG_03351":null,"SJAG_03385":null,"SJAG_03417":null,"SJAG_03454":null,"SJAG_03561":null,"SJAG_03575":null,"SJAG_03651":null,"SJAG_03680":null,"SJAG_03728":null,"SJAG_03809":null,"SJAG_03841":null,"SJAG_03858":null,"SJAG_04035":null,"SJAG_04087":null,"SJAG_04142":null,"SJAG_04151":null,"SJAG_04309":null,"SJAG_04335":null,"SJAG_04384":null,"SJAG_04520":null,"SJAG_04540":null,"SJAG_04574":null,"SJAG_04612":null,"SJAG_04619":null,"SJAG_04661":null,"SJAG_04853":null,"SJAG_04971":null,"SJAG_05012":null,"SJAG_05236":null,"SJAG_05274":null,"SJAG_05297":null,"SJAG_05329":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"ubiquitin ligase complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0000151","terms_by_termid":{"GO:0000151":null,"GO:0000836":null,"GO:0005680":null,"GO:0019005":null,"GO:0031461":null,"GO:0031463":null,"GO:0031464":null,"GO:0033503":null,"GO:0033768":null,"GO:0034657":null,"GO:0035361":null,"GO:0043224":null,"GO:0043494":null,"GO:0044695":null,"GO:0080008":null,"GO:0097505":null}}


id: PBO:0062055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily W member 2 pseudogene","termid":"PBO:0062055"}


id: GO:0006696
data:
  {"annotated_genes":["SJAG_03509","SJAG_03018","SJAG_04810","SJAG_04217","SJAG_02104","SJAG_04018","SJAG_04270","SJAG_00370","SJAG_01307","SJAG_02982","SJAG_00413","SJAG_01474","SJAG_03249","SJAG_04499","SJAG_03531","SJAG_00624","SJAG_03929","SJAG_00453","SJAG_02855","SJAG_03235","SJAG_00770","SJAG_02044","SJAG_03715","SJAG_03598","SJAG_03024","SJAG_02719","SJAG_03750","SJAG_00717"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67109,71606,72680,73299,73505,74922,75728,76073,77914,78271,78279,79008,81916,82102,82128,90346,91539,96540,109505,109819,111235,112077,117252,118568],"is_not":false,"summary":null,"term":"GO:0006696"},{"annotations":[95777],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0010895"},{"annotations":[111843],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0070452"},{"annotations":[90435,107806],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032443"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ergosterol, (22E)-ergosta-5,7,22-trien-3-beta-ol, a sterol found in ergot, yeast and moulds.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ergosterol metabolic process","termid":"GO:0008204"},{"relation_name":"is_a","term_name":"sterol biosynthetic process","termid":"GO:0016126"},{"relation_name":"is_a","term_name":"phytosteroid biosynthetic process","termid":"GO:0016129"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00370":null,"SJAG_00413":null,"SJAG_00453":null,"SJAG_00624":null,"SJAG_00717":null,"SJAG_00770":null,"SJAG_01307":null,"SJAG_01474":null,"SJAG_02044":null,"SJAG_02104":null,"SJAG_02719":null,"SJAG_02855":null,"SJAG_02982":null,"SJAG_03018":null,"SJAG_03024":null,"SJAG_03235":null,"SJAG_03249":null,"SJAG_03509":null,"SJAG_03531":null,"SJAG_03598":null,"SJAG_03715":null,"SJAG_03750":null,"SJAG_03929":null,"SJAG_04018":null,"SJAG_04217":null,"SJAG_04270":null,"SJAG_04499":null,"SJAG_04810":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"ergosterol biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"ergosterol anabolism","type":"exact"},{"name":"ergosterol biosynthesis","type":"exact"},{"name":"ergosterol formation","type":"exact"},{"name":"ergosterol synthesis","type":"exact"}],"termid":"GO:0006696","terms_by_termid":{"GO:0006696":null,"GO:0010895":null,"GO:0032443":null,"GO:0070452":null}}


id: GO:0009480
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 class IIb cytochrome c (obsolete GO:0009480)","synonyms":[{"name":"class IIb cytochrome c","type":"exact"}],"termid":"GO:0009480"}


id: PBO:0086196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that activates Rub1p (NEDD8) before neddylation; acts together with Ula1p; may play a role in protein degradation; GFP-fusion protein localizes to the cytoplasm in a punctate pattern","termid":"PBO:0086196"}


id: GO:1990053
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: DNA containing 5-methylcytosine + H2O = DNA with abasic site + 5-methylcytosine. This reaction is the hydrolysis of DNA by cleavage of the N-C1' glycosidic bond between the DNA 5-methylcytosine and the deoxyribose sugar to remove the 5-methylcytosine, leaving an abasic site.","definition_xrefs":["PMID:23316050"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkylbase DNA N-glycosylase activity","termid":"GO:0003905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140097","GO:0016798","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"DNA-5-methylcytosine glycosylase activity","termid":"GO:1990053"}


id: GO:2000692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of seed maturation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of seed maturation","termid":"GO:2000034"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"negatively_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":"negative regulation of seed maturation","termid":"GO:2000692"}


id: GO:0043132
data:
  {"annotated_genes":["SJAG_04328"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94798],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990549"}]},"cv_name":"biological_process","definition":"The directed movement of nicotinamide adenine dinucleotide into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore; transport may be of either the oxidized form, NAD, or the reduced form, NADH.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenine nucleotide transport","termid":"GO:0051503"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04328":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:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"NAD transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"NAD (oxidized) transport","type":"exact"},{"name":"NAD (reduced) transport","type":"exact"},{"name":"NADH transport","type":"exact"},{"name":"nicotinamide adenine dinucleotide transport","type":"exact"},{"name":"oxidized NAD transport","type":"exact"},{"name":"oxidized nicotinamide adenine dinucleotide transport","type":"exact"},{"name":"reduced NAD transport","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide transport","type":"exact"}],"termid":"GO:0043132","terms_by_termid":{"GO:1990549":null}}


id: MONDO:0020979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hamartoma characterized by localized pilosebaceous apparatus malformation.","definition_xrefs":["NCIT:C5565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hamartoma of skin appendage","termid":"MONDO:0021539"}],"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":"pilosebaceous hamartoma","secondary_identifiers":["icd11.foundation:59912591","MEDGEN:277515","UMLS:C1335410"],"synonyms":[{"name":"pilosebaceous hamartoma","type":"exact"}],"termid":"MONDO:0020979","xrefs":{"Monarch":{"xref_id":"0020979"}}}


id: MONDO:0003286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from an extrahepatic bile duct. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C5855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver leiomyoma","termid":"MONDO:0004723"},{"relation_name":"is_a","term_name":"extrahepatic bile duct neoplasm","termid":"MONDO:0021385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"extrahepatic bile duct leiomyoma","secondary_identifiers":["UMLS:C1333507","DOID:5125","MEDGEN:232169"],"synonyms":[{"name":"extrahepatic bile duct leiomyoma","type":"exact"},{"name":"leiomyoma of extrahepatic bile duct","type":"exact"},{"name":"leiomyoma of the extrahepatic bile duct","type":"exact"}],"termid":"MONDO:0003286","xrefs":{"Monarch":{"xref_id":"0003286"}}}


id: MONDO:1012688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lysosomal storage disease that occurs in pigs due to a mutation in the HEXA gene.","definition_xrefs":["OMIA:001461-9823"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gangliosidosis, pig","termid":"MONDO:1010842"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GM2 gangliosidosis, HEXA-related, pig","synonyms":[{"name":"gangliosidosis, GM2, type I (B variant), pig","type":"related"}],"termid":"MONDO:1012688","xrefs":{"Monarch":{"xref_id":"1012688"}}}


id: PBO:0071834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 29","termid":"PBO:0071834"}


id: PBO:0027509
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_mitotic_chromosome_condensation","termid":"PBO:0027509"}


id: PBO:0013764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy protein Atg14","termid":"PBO:0013764"}


id: PBO:0075813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSBP3 pseudogene 2","termid":"PBO:0075813"}


id: GO:1904756
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of gut granule assembly.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:17535251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of organelle assembly","termid":"GO:1902116"},{"relation_name":"is_a","term_name":"regulation of gut granule assembly","termid":"GO:1904755"},{"relation_name":"negatively_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:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of gut granule assembly","synonyms":[{"name":"down regulation of gut granule assembly","type":"exact"},{"name":"down regulation of gut granule biogenesis","type":"exact"},{"name":"down regulation of gut granule formation","type":"exact"},{"name":"down-regulation of gut granule assembly","type":"exact"},{"name":"down-regulation of gut granule biogenesis","type":"exact"},{"name":"down-regulation of gut granule formation","type":"exact"},{"name":"downregulation of gut granule assembly","type":"exact"},{"name":"downregulation of gut granule biogenesis","type":"exact"},{"name":"downregulation of gut granule formation","type":"exact"},{"name":"inhibition of gut granule assembly","type":"narrow"},{"name":"inhibition of gut granule biogenesis","type":"narrow"},{"name":"inhibition of gut granule formation","type":"narrow"},{"name":"negative regulation of gut granule biogenesis","type":"exact"},{"name":"negative regulation of gut granule formation","type":"exact"}],"termid":"GO:1904756"}


id: PBO:0071802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulation of nuclear pre-mRNA domain containing 2","termid":"PBO:0071802"}


id: GO:0102056
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3'-phosphonato-5'-adenylyl sulfate + an 11-hydroxyjasmonate = adenosine 3',5'-bismonophosphate + H+ + an 11-hydroxyjasmonate sulfate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 11-hydroxyjasmonate sulfotransferase activity (obsolete GO:0102056)","termid":"GO:0102056"}


id: PBO:0076565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 3F","termid":"PBO:0076565"}


