# terms

id: GO:0098900
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of action potential creation, propagation or termination. This typically occurs via modulation of the activity or expression of voltage-gated ion channels.","definition_xrefs":["GOC:go_curators","GOC:dos","GOC:tb","ISBN:978-0-07-139011-8","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane potential","termid":"GO:0042391"},{"relation_name":"is_a","term_name":"regulation of biological process","termid":"GO:0050789"},{"relation_name":"regulates","term_name":"action potential","termid":"GO:0001508"}],"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","termid":"GO:0098900"}


id: FYPO:0007886
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 dimethylation of lysine at position 9 of histone H3 does not occur.","definition_xrefs":["PMID:34524082","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished histone H3-K9 methylation during vegetative growth","termid":"FYPO:0002566"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0002274","FYPO:0001320"],"is_obsolete":false,"name":"abolished histone H3-K9 dimethylation during vegetative growth","synonyms":[{"name":"abolished histone H3 K9 dimethylation during vegetative growth","type":"exact"},{"name":"abolished histone H3-K9 dimethylation during mitotic cell cycle","type":"related"},{"name":"abolished histone H3K9me2 during vegetative growth","type":"exact"},{"name":"abolished histone lysine H3 K9 dimethylation during vegetative growth","type":"exact"},{"name":"histone H3-K9 dimethylation abolished during vegetative growth","type":"exact"},{"name":"histone H3-K9 dimethylation absent during vegetative growth","type":"exact"}],"termid":"FYPO:0007886"}


id: GO:0006035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of cuticle chitin, a linear polysaccharide consisting of beta-(1->4)-linked N-acetyl-D-glucosamine residues, found in cuticles.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cuticle chitin biosynthetic process (obsolete GO:0006035)","synonyms":[{"name":"cuticle chitin anabolism","type":"exact"},{"name":"cuticle chitin biosynthesis","type":"exact"},{"name":"cuticle chitin formation","type":"exact"},{"name":"cuticle chitin synthesis","type":"exact"}],"termid":"GO:0006035"}


id: GO:0097183
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex that contains protein C inhibitor (SERPINA5) and coagulation factor XI (F11); formation of the complex inhibits the serine protease activity of coagulation factor XI.","definition_xrefs":["PMID:2844223","GOC:ans"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine protease inhibitor complex","termid":"GO:0097180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"protein C inhibitor-coagulation factor XI complex","synonyms":[{"name":"PCI-coagulation factor XI complex","type":"exact"},{"name":"SERPINA5-coagulation factor XI complex","type":"exact"},{"name":"plasma serine protease inhibitor-coagulation factor XI complex","type":"exact"},{"name":"protein C inhibitor-F11 complex","type":"exact"},{"name":"serpin A5-coagulation factor XI complex","type":"exact"}],"termid":"GO:0097183"}


id: MONDO:1011209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited disorder affecting the structure, composition, and quantity of tooth enamel in dogs due to a variation in the ACP4 gene.","definition_xrefs":["PMID:30877375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amelogenesis imperfecta, non-human animal","termid":"MONDO:1012952"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amelogenesis imperfecta, ACP4-related, dog","secondary_identifiers":["OMIA:002177-9615"],"termid":"MONDO:1011209","xrefs":{"Monarch":{"xref_id":"1011209"}}}


id: PBO:0090239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane glucose/fructose:proton symporter Ght6","termid":"PBO:0090239"}


id: PBO:0048031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fascin actin-bundling protein 2, retinal","termid":"PBO:0048031"}


id: GO:1902974
data:
  {"annotated_genes":["SJAG_03720","SJAG_00364","SJAG_03438","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108432,104172,118073,90832],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1904514"}]},"cv_name":"biological_process","definition":"Any DNA replication initiation involved in meiotic cell cycle DNA replication.","definition_xrefs":["GOC:TermGenie","PMID:10888871","GO_REF:0000060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear cell cycle DNA replication initiation","termid":"GO:1902315"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_03048":null,"SJAG_03438":null,"SJAG_03720":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0007049","GO:0008150","GO:0006260"],"is_obsolete":false,"name":"meiotic DNA replication initiation","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0072691"],"synonyms":[{"name":"DNA replication initiation involved in meiotic DNA replication","type":"exact"},{"name":"DNA replication initiation involved in meiotic cell cycle DNA replication","type":"exact"},{"name":"initiation of meiotic DNA synthesis","type":"related"},{"name":"initiation of premeiotic DNA replication","type":"related"},{"name":"initiation of premeiotic DNA synthesis","type":"related"},{"name":"premeiotic DNA replication initiation","type":"related"}],"termid":"GO:1902974","terms_by_termid":{"GO:1904514":null}}


id: PBO:0085344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phospholipase; preferentially hydrolyses phosphatidylserine, with minor activity against cardiolipin and phosphatidylethanolamine; required for lysis of autophagic and CVT bodies; targeted to intravacuolar vesicles during autophagy via the multivesicular body (MVB) pathway; required for the maintenance of lipid droplet quantity after the diauxic shift; regulates lipolysis; expression regulated by Yap1p during autophagy","termid":"PBO:0085344"}


id: PBO:0077562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 269","termid":"PBO:0077562"}


id: GO:2000785
data:
  {"annotated_genes":["SJAG_05289","SJAG_03851"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110380,110471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000786"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of autophagosome assembly.","definition_xrefs":["GOC:BHF","GOC:autophagy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vacuole organization","termid":"GO:0044088"},{"relation_name":"is_a","term_name":"regulation of organelle assembly","termid":"GO:1902115"},{"relation_name":"regulates","term_name":"autophagosome assembly","termid":"GO:0000045"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03851":null,"SJAG_05289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of autophagosome assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of PAS formation","type":"related"},{"name":"regulation of autophagic vacuole assembly","type":"exact"},{"name":"regulation of autophagic vacuole formation","type":"related"},{"name":"regulation of autophagosome biosynthesis","type":"exact"},{"name":"regulation of autophagosome formation","type":"exact"}],"termid":"GO:2000785","terms_by_termid":{"GO:2000786":null}}


id: GO:0033670
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of NAD kinase activity, the catalysis of the transfer of a phosphate group, usually from ATP, to an NAD molecule.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of NAD+ kinase activity (obsolete GO:0033670)","synonyms":[{"name":"NAD kinase regulator","type":"narrow"},{"name":"regulation of NAD kinase activity","type":"exact"}],"termid":"GO:0033670"}


id: PBO:0042305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD22 molecule","termid":"PBO:0042305"}


id: GO:1905833
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of microtubule nucleation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:27689799"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of microtubule nucleation","termid":"GO:0010968"},{"relation_name":"is_a","term_name":"negative regulation of microtubule polymerization","termid":"GO:0031115"},{"relation_name":"negatively_regulates","term_name":"microtubule nucleation","termid":"GO:0007020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0000226"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"negatively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0007010","GO:0044085","GO:0000226","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"negative regulation of microtubule nucleation","synonyms":[{"name":"down regulation of microtubule nucleation","type":"exact"},{"name":"down-regulation of microtubule nucleation","type":"exact"},{"name":"downregulation of microtubule nucleation","type":"exact"},{"name":"inhibition of microtubule nucleation","type":"narrow"}],"termid":"GO:1905833"}


id: PBO:0018152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA endoribonuclease involved in mRNP quality control Swt1 (predicted)","termid":"PBO:0018152"}


id: FYPO:0001472
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 tacrolimus during a cellular response to osmotic stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal growth during cellular response to osmotic stress","termid":"FYPO:0001021"},{"relation_name":"is_a","term_name":"normal growth on tacrolimus","termid":"FYPO:0001470"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0002057","FYPO:0000257","FYPO:0000139","FYPO:0000003","FYPO:0002060"],"is_obsolete":false,"name":"normal growth on tacrolimus during osmotic stress","synonyms":[{"name":"normal cell population growth in presence of tacrolimus during osmotic stress","type":"exact"},{"name":"normal cell population growth on tacrolimus and sorbitol","type":"narrow"},{"name":"normal cell population growth on tacrolimus during osmotic stress","type":"exact"},{"name":"normal cellular response to FK506 during osmotic stress","type":"exact"},{"name":"normal cellular response to tacrolimus and osmotic stress","type":"related"},{"name":"normal cellular response to tacrolimus and sorbitol","type":"related"},{"name":"normal cellular response to tacrolimus during osmotic stress","type":"related"},{"name":"normal vegetative cell population growth on tacrolimus during osmotic stress","type":"exact"}],"termid":"FYPO:0001472"}


id: SO:0001983
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A 5' UTR variant where a premature start codon is introduced, moved or lost.","definition_xrefs":["SANGER:am"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5_prime_UTR_variant","termid":"SO:0001623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5_prime_UTR_premature_start_codon_variant","synonyms":[{"name":"5' UTR premature start codon variant","type":"exact"}],"termid":"SO:0001983"}


id: PBO:0045311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNMT3L antisense RNA 1","termid":"PBO:0045311"}


id: GO:0016252
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any function that supports transcription of genes by RNA polymerase II, and is not specific to a particular gene or gene set.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete nonspecific RNA polymerase II transcription factor activity (obsolete GO:0016252)","synonyms":[{"name":"nonspecific RNA polymerase II transcription factor activity","type":"exact"}],"termid":"GO:0016252"}


id: PBO:0112564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane ammonium transmembrane transporter, high affinity Amt1","termid":"PBO:0112564"}


id: GO:0000131
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the budding yeast plasma membrane where a daughter cell will emerge. The yeast marks this spot with bud-site selection proteins before bud emergence occurs. Actin is polarized to this spot just prior to and during bud emergence.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"site of polarized growth","termid":"GO:0030427"}],"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":"incipient cellular bud site","termid":"GO:0000131"}


id: PBO:0003183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory subunit Rpn7","termid":"PBO:0003183"}


id: PBO:0046083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4A1 pseudogene 8","termid":"PBO:0046083"}


id: PATO:0002299
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A cylindrical shape that is hollow.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cylindrical","termid":"PATO:0001873"},{"relation_name":"is_a","term_name":"hollow","termid":"PATO:0002078"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubular","synonyms":[{"name":"tube like","type":"exact"},{"name":"tube-shaped","type":"exact"},{"name":"tubulate","type":"exact"}],"termid":"PATO:0002299"}


id: GO:0003942
data:
  {"annotated_genes":["SJAG_00636"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73106],"is_not":false,"summary":null,"term":"GO:0003942"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acetyl-L-glutamate 5-semialdehyde + NADP+ + phosphate = N-acetyl-5-glutamyl phosphate + NADPH + H+.","definition_xrefs":["RHEA:21588"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00636":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"N-acetyl-gamma-glutamyl-phosphate reductase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:N-ACETYLGLUTPREDUCT-RXN","EC:1.2.1.38"],"synonyms":[{"name":"N-acetyl-L-glutamate gamma-semialdehyde:NADP oxidoreductase (phosphorylating)","type":"related"},{"name":"N-acetyl-L-glutamate-5-semialdehyde:NADP+ 5-oxidoreductase (phosphorylating)","type":"related"},{"name":"N-acetyl-glutamate semialdehyde dehydrogenase activity","type":"related"},{"name":"N-acetylglutamate 5-semialdehyde dehydrogenase activity","type":"related"},{"name":"N-acetylglutamic gamma-semialdehyde dehydrogenase activity","type":"related"},{"name":"NAGSA dehydrogenase activity","type":"broad"},{"name":"reductase, acetyl-gamma-glutamyl phosphate","type":"related"}],"termid":"GO:0003942","terms_by_termid":{"GO:0003942":null}}


id: PBO:0040223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATE1 opposite strand, pseudogene","termid":"PBO:0040223"}


id: PBO:0080051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 22","termid":"PBO:0080051"}


id: PBO:0042565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDKN1A antisense RNA 1","termid":"PBO:0042565"}


id: GO:0005588
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen heterotrimer containing type V alpha chains; [alpha1(V)]2alpha2(V) and alpha1(V)alpha2(V)alpha3(V) trimers have been observed; type V collagen triple helices associate to form fibrils.","definition_xrefs":["ISBN:0721639976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibrillar collagen trimer","termid":"GO:0005583"}],"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":"collagen type V trimer","termid":"GO:0005588"}


id: PBO:0074388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMG9 nonsense mediated mRNA decay factor","termid":"PBO:0074388"}


id: GO:0009056
data:
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id: PBO:0049613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 16","termid":"PBO:0049613"}


id: PBO:0001460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetyl-gamma-glutamyl-phosphate reductase/acetylglutamate kinase","termid":"PBO:0001460"}


id: PR:O13901
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ethanolaminephosphotransferase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00472"],"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 CDP-alcohol phosphatidyltransferase class-I family protein C22A12.10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22A12.10","secondary_identifiers":["UniProtKB:O13901"],"synonyms":[{"name":"Spom972h-EPT1","type":"exact"}],"termid":"PR:O13901"}


id: GO:0070561
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A nuclear receptor-mediated signaling pathway initiated by vitamin D binding to an intracellular receptor of the nuclear receptor protein family, and ending with regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:BHF","GOC:mah","PMID:12637589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone-mediated signaling pathway","termid":"GO:0009755"},{"relation_name":"is_a","term_name":"nuclear receptor-mediated signaling pathway","termid":"GO:0141193"},{"relation_name":"part_of","term_name":"cellular response to vitamin D","termid":"GO:0071305"}],"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":"vitamin D receptor signaling pathway","synonyms":[{"name":"VDR signaling pathway","type":"exact"},{"name":"calcitriol signaling pathway","type":"narrow"},{"name":"intracellular vitamin D receptor signaling pathway","type":"exact"},{"name":"nuclear receptor-mediated vitamin D signaling pathway","type":"exact"},{"name":"vitamin D receptor signalling pathway","type":"exact"}],"termid":"GO:0070561"}


id: MONDO:0001633
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Blockage of the central retinal artery.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal artery occlusion","termid":"MONDO:0006948"},{"relation_name":"is_a","term_name":"arterial occlusion","termid":"MONDO:0020673"}],"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":"central retinal artery occlusion","secondary_identifiers":["UMLS:C0007688","DOID:13098","Orphanet:648684","ICD10CM:H34.1","MEDGEN:40177","SCTID:38742007","NCIT:C34456","icd11.foundation:613330234","ICD9:362.31"],"synonyms":[{"name":"central retinal arterial occlusion","type":"exact"}],"termid":"MONDO:0001633","xrefs":{"Monarch":{"xref_id":"0001633"}}}


id: PBO:0043144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 12","termid":"PBO:0043144"}


id: MOD:01937
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue to N-palmitoyl-L-methionine.","definition_xrefs":["PubMed:20942504","RESID:AA0591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"},{"relation_name":"is_a","term_name":"alpha-amino palmitoylated residue","termid":"MOD:01685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"N-palmitoyl-L-methionine","synonyms":[{"name":"(2S)-2-(hexadecanoylamino)-4-(methylsulfanyl)butanoic acid","type":"exact"},{"name":"2-(hexadecanamido)-4-(methylsulfanyl)butanoic acid","type":"exact"},{"name":"LIPID N-palmitoyl methionine","type":"exact"},{"name":"N-(1-oxohexadecyl)methionine","type":"exact"},{"name":"N-palmitoyl-L-methionine","type":"exact"}],"termid":"MOD:01937"}


id: PBO:0055665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LINGO1 antisense RNA 2","termid":"PBO:0055665"}


id: PBO:0044889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEP domain containing 1B","termid":"PBO:0044889"}


id: GO:0005968
data:
  {"annotated_genes":["SJAG_02063","SJAG_03810","SJAG_04434"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[75512,80651,81233],"is_not":false,"summary":null,"term":"GO:0005968"}]},"cv_name":"cellular_component","definition":"An protein-containing complex which catalyzes of the transfer of a geranyl-geranyl group from geranylgeranyl pyrophosphate to a Rab protein. In mammals it is composed of an alpha and a beta subunit, and associates with an accessory protein Rep (Rab escort protein).","definition_xrefs":["PMID:11886217","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02063":null,"SJAG_03810":null,"SJAG_04434":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"Rab-protein geranylgeranyltransferase complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"GGTase-II complex","type":"exact"},{"name":"Rab geranylgeranyltransferase complex","type":"exact"},{"name":"RabGGTase complex","type":"exact"}],"termid":"GO:0005968","terms_by_termid":{"GO:0005968":null}}


id: PBO:0079277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TELO2 interacting protein 1","termid":"PBO:0079277"}


id: GO:0010260
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process that occurs in an animal organ near the end of its active life that is associated with the dismantling of cell components and membranes, and an overall decline in metabolism.","definition_xrefs":["GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete animal organ senescence (obsolete GO:0010260)","termid":"GO:0010260"}


id: MONDO:0004356
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cystic neoplasm which arises from the kidney and occurs in children. It includes the cystic partially differentiated nephroblastoma and cases in which nephroblastomatous elements are not present.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood kidney neoplasm","termid":"MONDO:0002730"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"childhood multilocular cystic kidney neoplasm","secondary_identifiers":["NCIT:C6566","MEDGEN:232064","UMLS:C1332983","DOID:7762"],"synonyms":[{"name":"benign multilocular cystic renal tumor","type":"related"},{"name":"benign multilocular cystic renal tumour","type":"related"},{"name":"childhood multilocular cystic kidney neoplasm","type":"exact"},{"name":"childhood multilocular cystic kidney tumor","type":"exact"},{"name":"childhood multilocular cystic kidney tumour","type":"exact"},{"name":"childhood multilocular cystic renal neoplasm","type":"exact"},{"name":"childhood multilocular cystic renal tumor","type":"exact"},{"name":"childhood multilocular cystic renal tumour","type":"exact"},{"name":"paediatric multilocular cystic kidney neoplasm","type":"exact"},{"name":"paediatric multilocular cystic kidney tumour","type":"exact"},{"name":"paediatric multilocular cystic renal neoplasm","type":"exact"},{"name":"paediatric multilocular cystic renal tumour","type":"exact"},{"name":"pediatric multilocular cystic kidney neoplasm","type":"exact"},{"name":"pediatric multilocular cystic kidney tumor","type":"exact"},{"name":"pediatric multilocular cystic renal neoplasm","type":"exact"},{"name":"pediatric multilocular cystic renal tumor","type":"exact"}],"termid":"MONDO:0004356","xrefs":{"Monarch":{"xref_id":"0004356"}}}


id: PBO:0069306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 562, pseudogene","termid":"PBO:0069306"}


id: GO:0038151
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of the C-C chemokine CCL2 to a C-C chemokine type 2 receptor (CCR2) on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:nhn","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine (C-C motif) ligand 2 signaling pathway","termid":"GO:0038148"},{"relation_name":"is_a","term_name":"C-C chemokine receptor CCR2 signaling pathway","termid":"GO:0038150"}],"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":"CCL2-activated CCR2 signaling pathway","synonyms":[{"name":"CCL2/CCR2 signaling pathway","type":"exact"}],"termid":"GO:0038151"}


id: MONDO:0004177
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormal growth of the cells of the urethra (lower urinary tract) without malignant characteristics.","definition_xrefs":["NCIT:C3619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign urinary system neoplasm","termid":"MONDO:0004180"},{"relation_name":"is_a","term_name":"urethra neoplasm","termid":"MONDO:0021239"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign urethral neoplasm","secondary_identifiers":["DOID:730","UMLS:C0154019","MEDGEN:57812","ICD10CM:D30.4","ICD9:223.81","SCTID:92466006"],"synonyms":[{"name":"benign neoplasm of the urethra","type":"exact"},{"name":"benign neoplasm of urethra","type":"exact"},{"name":"benign tumor of the urethra","type":"exact"},{"name":"benign tumor of urethra","type":"exact"},{"name":"benign tumour of the urethra","type":"exact"},{"name":"benign tumour of urethra","type":"exact"},{"name":"benign urethra neoplasm","type":"exact"},{"name":"benign urethra tumor","type":"exact"},{"name":"benign urethra tumour","type":"exact"},{"name":"benign urethral neoplasm","type":"exact"},{"name":"benign urethral tumor","type":"exact"},{"name":"benign urethral tumour","type":"exact"},{"name":"neoplasm. urethra","type":"exact"},{"name":"urethra benign neoplasm","type":"exact"},{"name":"urethral benign neoplasm","type":"related"}],"termid":"MONDO:0004177","xrefs":{"Monarch":{"xref_id":"0004177"}}}


id: MONDO:0006008
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic inflammation of the vestibular nerve, characterized clinically by the acute or subacute onset of vertigo; nausea; and imbalance. The cochlear nerve is typically spared and hearing loss and tinnitus do not usually occur. Symptoms usually resolve over a period of days to weeks. (Adams et al., Principles of Neurology, 6th ed, p304)","definition_xrefs":["MESH:D020338"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibulocochlear nerve disorder","termid":"MONDO:0001563"},{"relation_name":"is_a","term_name":"neuritis","termid":"MONDO:0002122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"vestibular neuronitis","secondary_identifiers":["ICD10CM:H81.2","ICD9:386.12","MEDGEN:155655","EFO:0007537","DOID:12683","ICD9:078.81","SCTID:186738001","UMLS:C0751908"],"synonyms":[{"name":"epidemic neurolabyrinthitis","type":"exact"},{"name":"vestibular neuritis","type":"exact"}],"termid":"MONDO:0006008","xrefs":{"Monarch":{"xref_id":"0006008"}}}


id: PBO:0036385
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by Bulleromyces albus DPS1","termid":"PBO:0036385"}


id: GO:0039644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces a host NF-kappaB cascade.","definition_xrefs":["PMID:25275128","PMID:10920188"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host NF-kappaB cascade (obsolete GO:0039644)","synonyms":[{"name":"inhibition of host NF-kappa-B by virus","type":"exact"},{"name":"suppression by virus of host NF-kappaB transcription factor activity","type":"related"}],"termid":"GO:0039644"}


id: MOD:00861
data:
  {"annotated_genes":["SJAG_02183","SJAG_00331","SJAG_02498","SJAG_02592","SJAG_04972","SJAG_01671","SJAG_03012","SJAG_02763","SJAG_04551","SJAG_00318","SJAG_02472","SJAG_01587"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[82389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00226"},{"annotations":[82271,82292,82364,82414,82372,82208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00042"},{"annotations":[121315,121156,82432,82433,121157,121317,121318,121316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00046"},{"annotations":[82361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00159"},{"annotations":[120971,121206,121207,121208,121494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00696"}]},"cv_name":"PSI-MOD","definition":"A protein modification that produces an amino acid residue containing a phosphorus atom.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00318":null,"SJAG_00331":null,"SJAG_01587":null,"SJAG_01671":null,"SJAG_02183":null,"SJAG_02472":null,"SJAG_02498":null,"SJAG_02592":null,"SJAG_02763":null,"SJAG_03012":null,"SJAG_04551":null,"SJAG_04972":null},"genotype_count":0,"is_obsolete":false,"name":"phosphorus containing modified residue","references_by_uniquename":{"PMID:26774782":null,"PMID:31150379":null,"PMID:32915139":null,"PMID:33791858":null,"PMID:34198697":null,"PMID:36408920":null},"termid":"MOD:00861","terms_by_termid":{"GO:0034599":null,"GO:0034605":null,"GO:0036460":null,"GO:0042149":null,"GO:0071475":null,"GO:0120306":null,"GO:1904547":null,"MOD:00042":null,"MOD:00046":null,"MOD:00159":null,"MOD:00226":null,"MOD:00696":null}}


id: PBO:0113444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit a of vacuolar-ATPase V0 domain; encodes one of two isoforms, located in both Golgi and endosomal V-ATPase complexes while VPH1 encodes second isoform and is located in vacuolar V-ATPase complexes; interaction with PI(4)P is required for efficient localization and function of Stv1-containing V-ATPases; targeted to vacuole via AP-3 pathway","termid":"PBO:0113444"}


id: MONDO:0013985
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the OTOG gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 18B","secondary_identifiers":["UMLS:C3554163","DOID:0110474","MEDGEN:767077","GARD:22648","OMIM:614945"],"synonyms":[{"name":"DFNB18B","type":"narrow"},{"name":"OTOG autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 18B","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 18B","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in OTOG","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 18B","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 18B","type":"exact"},{"name":"deafness, autosomal recessive 18B","type":"narrow"},{"name":"deafness, autosomal recessive 18b","type":"narrow"},{"name":"deafness, autosomal recessive type 18B","type":"narrow"}],"termid":"MONDO:0013985","xrefs":{"Monarch":{"xref_id":"0013985"}}}


id: GO:0051902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the change in the membrane potential of the mitochondria from negative to positive.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitochondrial depolarization","termid":"GO:0051900"},{"relation_name":"is_a","term_name":"negative regulation of membrane depolarization","termid":"GO:1904180"},{"relation_name":"negatively_regulates","term_name":"mitochondrial depolarization","termid":"GO:0051882"}],"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 mitochondrial depolarization","synonyms":[{"name":"down regulation of mitochondrial depolarization","type":"exact"},{"name":"down-regulation of mitochondrial depolarization","type":"exact"},{"name":"downregulation of mitochondrial depolarization","type":"exact"},{"name":"inhibition of mitochondrial depolarization","type":"narrow"}],"termid":"GO:0051902"}


id: FYPO:0009076
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is increased relative to normal in a medium containing sucrose as the carbon source.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0005447","FYPO:0002058","FYPO:0000003","FYPO:0001985","FYPO:0002057"],"is_obsolete":false,"name":"increased cell population growth on sucrose carbon source","synonyms":[{"name":"increased growth on sucrose carbon source","type":"broad"},{"name":"increased vegetative cell growth on sucrose carbon source","type":"exact"}],"termid":"FYPO:0009076"}


id: GO:0032405
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a MutLalpha mismatch repair complex.","definition_xrefs":["GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mismatch repair complex binding","termid":"GO:0032404"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"MutLalpha complex binding","termid":"GO:0032405"}


id: MONDO:0005103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A locally aggressive malignant neoplasm composed of mature adipocytes showing cell size variation and nuclear atypia. It is often associated with the presence of hyperchromatic multinucleated stromal cells, and varying numbers of lipoblasts. There are three histologic subtypes, sclerosing, inflammatory, and spindle cell liposarcoma. These tumors do not usually metastasize unless they undergo dedifferentiation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"well-differentiated liposarcoma","secondary_identifiers":["ONCOTREE:WDLS","NCIT:C4250","ICDO:8851/3","MEDGEN:237164","UMLS:C1370889","EFO:0000736","GARD:19721","Orphanet:99971"],"synonyms":[{"name":"ALT","type":"exact"},{"name":"WDLS","type":"exact"},{"name":"atypical lipoma","type":"exact"},{"name":"atypical lipomatous tumor","type":"broad"},{"name":"atypical lipomatous tumour","type":"broad"},{"name":"well differentiated liposarcoma","type":"exact"},{"name":"well differentiated liposarcoma of deep soft tissue","type":"exact"},{"name":"well-differentiated liposarcoma","type":"exact"}],"termid":"MONDO:0005103","xrefs":{"Monarch":{"xref_id":"0005103"}}}


id: PBO:0011469
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"this is not NADH complex associated in yeast (which do not have the other 40 subunits that are present in that complex in mammals), possibly involved in iron sulpher protein assembly or lipid metabolism, see associated refs for more info on the human protein","termid":"PBO:0011469"}


id: PBO:0081536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 445","termid":"PBO:0081536"}


id: PBO:0086269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein translocase and chaperone required for Complex III assembly; member of the AAA ATPase family; forms a homo-oligomeric complex in the mitochondrial inner membrane that translocates the C-terminal domain of Rip1p from the matrix across the inner membrane and delivers it to an assembly intermediate of respiratory Complex III; also required for assembly of the Qcr10p subunit; mutation is functionally complemented by human homolog BCS1L, linked to neonatal diseases","termid":"PBO:0086269"}


id: GO:0043457
data:
  {"annotated_genes":["SJAG_02592","SJAG_02433","SJAG_00698","SJAG_01062"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113711,99408,111514,96150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903715"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular respiration, the enzymatic release of energy from organic compounds.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of generation of precursor metabolites and energy","termid":"GO:0043467"},{"relation_name":"regulates","term_name":"cellular respiration","termid":"GO:0045333"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00698":null,"SJAG_01062":null,"SJAG_02433":null,"SJAG_02592":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"regulation of cellular respiration","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0043457","terms_by_termid":{"GO:1903715":null}}


id: PBO:0080691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WNK lysine deficient protein kinase 3","termid":"PBO:0080691"}


id: PBO:0013443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMARCAD1 family ATP-dependent DNA helicase Fft1 (predicted)","termid":"PBO:0013443"}


id: GO:0045905
data:
  {"annotated_genes":["SJAG_02812","SJAG_05265","SJAG_02189"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67770,70235,78222],"is_not":false,"summary":null,"term":"GO:0045905"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of translational termination.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translational termination","termid":"GO:0006449"},{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex disassembly","termid":"GO:0043243"},{"relation_name":"is_a","term_name":"positive regulation of translation","termid":"GO:0045727"},{"relation_name":"positively_regulates","term_name":"translational termination","termid":"GO:0006415"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02189":null,"SJAG_02812":null,"SJAG_05265":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of translational termination","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null},"synonyms":[{"name":"activation of translational termination","type":"narrow"},{"name":"stimulation of translational termination","type":"narrow"},{"name":"up regulation of translational termination","type":"exact"},{"name":"up-regulation of translational termination","type":"exact"},{"name":"upregulation of translational termination","type":"exact"}],"termid":"GO:0045905","terms_by_termid":{"GO:0045905":null}}


id: PBO:0004742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome C oxidase copper chaperone Cox17 (predicted)","termid":"PBO:0004742"}


id: PBO:0070627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 like 1 pseudogene 11","termid":"PBO:0070627"}


id: MONDO:0013069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An optic atrophy that is caused by a mutation in the TMEM126A gene.","definition_xrefs":["OMIM:612989"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"hereditary optic atrophy","termid":"MONDO:0043878"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005559","MONDO:0005066"],"is_obsolete":false,"name":"autosomal recessive optic atrophy, OPA7 type","secondary_identifiers":["MEDGEN:414112","MESH:C567833","GARD:17143","Orphanet:227976","DOID:0111437","UMLS:C2751812"],"synonyms":[{"name":"OPA7","type":"related"},{"name":"TMEM126A-related optic atrophy with or without extraocular features","type":"exact"},{"name":"optic atrophy 7","type":"exact"},{"name":"optic atrophy 7 with or without auditory neuropathy","type":"related"}],"termid":"MONDO:0013069","xrefs":{"Monarch":{"xref_id":"0013069"}}}


id: PBO:0062921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P2Y receptor family member 8","termid":"PBO:0062921"}


id: MONDO:0100348
data:
  {"annotated_genes":["SJAG_02517"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87515],"is_not":false,"summary":null,"term":"MONDO:0100348"}]},"cv_name":"mondo","definition":"An autosomal recessive disorder characterized by global developmental delay apparent in infancy. Affected individuals have delayed walking with variable gait abnormalities, impaired intellectual development with poor or absent speech and language, and progressive microcephaly. More variable features include hypotonia, early-onset seizures, and a peripheral demyelinating or axonal peripheral sensorimotor neuropathy. The disease follows a neurodegenerative course in many patients; clinical features suggest involvement of both the central and peripheral nervous systems.","definition_xrefs":["OMIM:619091"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02517":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0006025"],"is_obsolete":false,"name":"neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1731507","GARD:18534","UMLS:C5436783"],"synonyms":[{"name":"NEDMILG, AR","type":"exact"},{"name":"neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive","type":"exact"}],"termid":"MONDO:0100348","terms_by_termid":{"MONDO:0100348":null},"xrefs":{"Monarch":{"xref_id":"0100348"}}}


id: GO:0009881
data:
  {"annotated_genes":["SJAG_02860"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[121260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009882"}]},"cv_name":"molecular_function","definition":"The function of absorbing and responding to incidental electromagnetic radiation, particularly visible light. The response may involve a change in conformation.","definition_xrefs":["GOC:ai","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor activity","termid":"GO:0038023"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02860":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"photoreceptor activity","references_by_uniquename":{"PMID:23873862":null},"synonyms":[{"name":"UV-sensitive opsin","type":"narrow"},{"name":"blue-sensitive opsin","type":"narrow"},{"name":"green-sensitive opsin","type":"narrow"},{"name":"long-wave-sensitive opsin","type":"narrow"},{"name":"opsin","type":"narrow"},{"name":"red-sensitive opsin","type":"narrow"},{"name":"short-wave-sensitive opsin","type":"narrow"},{"name":"violet-sensitive opsin","type":"narrow"}],"termid":"GO:0009881","terms_by_termid":{"GO:0009882":null}}


id: GO:0030744
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: S-adenosyl-L-methionine + luteolin = 4',5,7-trihydroxy-3'-methoxyflavone + S-adenosyl-L-homocysteine + H+.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete luteolin O-methyltransferase activity (obsolete GO:0030744)","termid":"GO:0030744"}


id: GO:0034435
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A lipid modification process in which a sterol ester is formed by the combination of a carboxylic acid (often a fatty acid) and cholesterol. In the blood this process is associated with the conversion of free cholesterol into cholesteryl ester, which is then sequestered into the core of a lipoprotein particle.","definition_xrefs":["GOC:pde","GOC:rl","GOC:BHF","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete cholesterol esterification (obsolete GO:0034435)","termid":"GO:0034435"}


id: PATO:0001153
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's lacking susceptibilty toward an external stimulus.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"susceptibility toward","termid":"PATO:0001043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insusceptible toward","synonyms":[{"name":"insusceptible","type":"exact"}],"termid":"PATO:0001153"}


id: PBO:0080431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS51 pseudogene 15","termid":"PBO:0080431"}


id: GO:2000452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of CD8-positive, alpha-beta cytotoxic T cell extravasation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of CD8-positive, alpha-beta T cell extravasation","termid":"GO:2000449"},{"relation_name":"regulates","term_name":"CD8-positive, alpha-beta cytotoxic T cell extravasation","termid":"GO:0035698"}],"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 CD8-positive, alpha-beta cytotoxic T cell extravasation","termid":"GO:2000452"}


id: GO:0047897
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7,8-dihydrofolate + ATP + formate = 10-formyldihydrofolate + ADP + H+ + phosphate.","definition_xrefs":["EC:6.3.4.17","RHEA:24328"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"formate-dihydrofolate ligase activity","secondary_identifiers":["MetaCyc:FORMATE--DIHYDROFOLATE-LIGASE-RXN","KEGG_REACTION:R02238"],"synonyms":[{"name":"dihydrofolate formyltransferase activity","type":"related"},{"name":"formate:dihydrofolate ligase (ADP-forming)","type":"related"},{"name":"formyl dihydrofolate synthase activity","type":"related"}],"termid":"GO:0047897"}


id: GO:0004496
data:
  {"annotated_genes":["SJAG_04865"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[81865],"is_not":false,"summary":null,"term":"GO:0004496"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-mevalonate + ATP = (R)-5-phosphomevalonate + ADP + 2 H+.","definition_xrefs":["RHEA:17065","EC:2.7.1.36"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04865":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"mevalonate kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:MEVALONATE-KINASE-RXN","Reactome:R-HSA-191380","KEGG_REACTION:R02245"],"synonyms":[{"name":"ATP:(R)-mevalonate 5-phosphotransferase activity","type":"related"},{"name":"ATP:mevalonate 5-phosphotransferase activity","type":"related"},{"name":"MVA kinase activity","type":"related"},{"name":"mevalonate 5-phosphotransferase activity","type":"related"},{"name":"mevalonate kinase (phosphorylating)","type":"related"},{"name":"mevalonate phosphokinase activity","type":"related"},{"name":"mevalonic acid kinase activity","type":"related"},{"name":"mevalonic kinase activity","type":"related"}],"termid":"GO:0004496","terms_by_termid":{"GO:0004496":null}}


id: GO:0006293
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The stabilization of the multiprotein complex involved in damage recognition, DNA helix unwinding, and endonucleolytic cleavage at the site of DNA damage as well as the unwound DNA. The stabilization of the protein-DNA complex ensures proper positioning of the preincision complex before the phosphodiester backbone of the damaged strand is cleaved 3' and 5' of the site of DNA damage.","definition_xrefs":["GOC:elh","PMID:10197977"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"part_of","term_name":"nucleotide-excision repair","termid":"GO:0006289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0008150","GO:0006281","GO:0044085","GO:0006259","GO:0065003"],"is_obsolete":false,"name":"nucleotide-excision repair, preincision complex stabilization","termid":"GO:0006293"}


id: GO:0047710
data:
  {"annotated_genes":["SJAG_04939"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[113282],"is_not":false,"summary":null,"term":"GO:0047710"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: P(1),P(3)-bis(5'-adenosyl) triphosphate + H2O = ADP + AMP + 2 H+.","definition_xrefs":["EC:3.6.1.29","RHEA:13893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04939":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"bis(5'-adenosyl)-triphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:BIS5-ADENOSYL-TRIPHOSPHATASE-RXN","KEGG_REACTION:R00187"],"synonyms":[{"name":"1-P,3-P-bis(5'-adenosyl)-triphosphate adenylohydrolase activity","type":"related"},{"name":"AP(3)A hydrolase activity","type":"related"},{"name":"AP(3)Aase activity","type":"related"},{"name":"AP3A hydrolase activity","type":"related"},{"name":"AP3Aase activity","type":"related"},{"name":"P1,P3-bis(5'-adenosyl)-triphosphate adenylohydrolase activity","type":"related"},{"name":"diadenosine 5',5'''-P(1),P(3)-triphosphate hydrolase activity","type":"related"},{"name":"diadenosine 5',5'''-P1,P3-triphosphate hydrolase activity","type":"related"},{"name":"diadenosine 5,5-P1,P3-triphosphatase activity","type":"related"},{"name":"dinucleosidetriphosphatase activity","type":"related"}],"termid":"GO:0047710","terms_by_termid":{"GO:0047710":null}}


id: GO:0102284
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-threo-sphinganine + NADP = H+ + NADPH + 3-dehydrosphinganinium(1+).","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete L-threo-sphinganine reductase activity (obsolete GO:0102284)","termid":"GO:0102284"}


id: GO:0033797
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 e(-) + 2 H+ + selenate = H2O + selenite.","definition_xrefs":["RHEA:14029"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity","termid":"GO:0016491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"selenate reductase activity","secondary_identifiers":["KEGG_REACTION:R07229","MetaCyc:RXN0-2101","UM-BBD_reactionID:r0828","EC:1.97.1.9"],"synonyms":[{"name":"selenite:reduced acceptor oxidoreductase activity","type":"related"}],"termid":"GO:0033797"}


id: MONDO:0005461
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma arising from the uterine body cavity. This is the most frequent malignant tumor affecting the uterine body, and is linked to estrogen therapy. Most patients present with uterine bleeding and are over age 40 at the time of diagnosis. The prognosis depends on the stage of the tumor, the depth of the uterine wall invasion, and the histologic subtype. Endometrioid adenocarcinoma is the most frequently seen morphologic variant of endometrial adenocarcinoma.","definition_xrefs":["NCIT:C7359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrial carcinoma","termid":"MONDO:0002447"},{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"endometrium adenocarcinoma","secondary_identifiers":["NCIT:C6287","UMLS:C1153706","DOID:2870","EFO:0005232","MEDGEN:218862"],"synonyms":[{"name":"adenocarcinoma of endometrium","type":"exact"},{"name":"adenocarcinoma of the endometrium","type":"exact"},{"name":"adenocarcinoma of uterus","type":"exact"},{"name":"adenocarcinoma, endometrial, malignant","type":"exact"},{"name":"endometrial adenoacanthoma","type":"exact"},{"name":"endometrial adenocarcinoma","type":"exact"},{"name":"endometrial endometrioid adenocarcinoma","type":"related"},{"name":"endometrial endometrioid adenocarcinoma with squamous differentiation","type":"exact"},{"name":"endometrioid adenoma or carcinoma","type":"exact"},{"name":"endometrioid adenoma or carcinoma NOS (morphologic abnormality)","type":"exact"},{"name":"endometrioid adenomas and carcinomas","type":"exact"},{"name":"endometrioid adenomas and carcinomas (morphologic abnormality)","type":"exact"},{"name":"endometrioid carcinoma of endometrium","type":"broad"},{"name":"endometrium adenocarcinoma","type":"exact"}],"termid":"MONDO:0005461","xrefs":{"Monarch":{"xref_id":"0005461"}}}


id: MOD:00723
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to either N2-acetyl-L-lysine, or N6-acetyl-L-lysine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetylated residue","termid":"MOD:00408"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00408"}],"interesting_parent_ids":["MOD:00408"],"is_obsolete":false,"name":"N-acetylated L-lysine","synonyms":[{"name":"NAcLys","type":"exact"}],"termid":"MOD:00723"}


id: PBO:0071222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 63","termid":"PBO:0071222"}


id: PBO:0117245
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine cleavage complex subunit H, Gcv3","termid":"PBO:0117245"}


id: PBO:0044955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenase/reductase 2","termid":"PBO:0044955"}


id: GO:1900784
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of fumiquinazoline F.","definition_xrefs":["GOC:di","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete fumiquinazoline F biosynthetic process (obsolete GO:1900784)","synonyms":[{"name":"fumiquinazoline F anabolism","type":"exact"},{"name":"fumiquinazoline F biosynthesis","type":"exact"},{"name":"fumiquinazoline F formation","type":"exact"},{"name":"fumiquinazoline F synthesis","type":"exact"}],"termid":"GO:1900784"}


id: PR:C6Y4B2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC57A7.15c gene.","definition_xrefs":["UniProtKB:C6Y4B2","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 C57A7.15c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A7.15c","synonyms":[{"name":"Spom972h-SPAC57A7.15c","type":"exact"}],"termid":"PR:C6Y4B2"}


id: PBO:0065833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB8A, member RAS oncogene family","termid":"PBO:0065833"}


id: MONDO:0017139
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oromandibular-limb hypogenesis syndromes (OLHS) are a group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) characterized by the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies).","definition_xrefs":["Orphanet:2749"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"oromandibular-limb anomalies syndrome","termid":"MONDO:0015498"}],"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":"oromandibular-limb hypogenesis syndrome","secondary_identifiers":["MEDGEN:1843329","UMLS:C5679764","GARD:4116","icd11.foundation:1665391511"],"synonyms":[{"name":"Oroacral syndrome","type":"exact"},{"name":"oro-mandibular-limb hypogenesis syndrome","type":"related"}],"termid":"MONDO:0017139","xrefs":{"Monarch":{"xref_id":"0017139"}}}


id: PBO:0072791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spalt like transcription factor 1 pseudogene 1","termid":"PBO:0072791"}


id: GO:0003300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The enlargement or overgrowth of all or part of the heart muscle due to an increase in size of cardiac muscle cells without cell division.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striated muscle hypertrophy","termid":"GO:0014897"}],"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":"cardiac muscle hypertrophy","termid":"GO:0003300"}


id: PBO:0073352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family B member 11","termid":"PBO:0073352"}


id: PBO:0045532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deltex E3 ubiquitin ligase 3","termid":"PBO:0045532"}


id: PBO:0050940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon alpha 11, pseudogene","termid":"PBO:0050940"}


id: GO:0031174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation and growth of otoliths throughout the life of the organism. Otoliths are the large extracellular ear-stones of the fish inner ear, produced by precipitation of specific crystal forms of calcium carbonate on organic matrices. The otolith enlarges throughout the life of the fish, as layers of calcium carbonate are added.","definition_xrefs":["GOC:dsf","PMID:15581873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otolith mineralization","termid":"GO:0045299"}],"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":"lifelong otolith mineralization","termid":"GO:0031174"}


id: GO:0008235
data:
  {"annotated_genes":["SJAG_00969","SJAG_00181","SJAG_00451","SJAG_01542","SJAG_01088","SJAG_01896","SJAG_06636","SJAG_03022","SJAG_04858","SJAG_03586","SJAG_03009","SJAG_04103","SJAG_02033","SJAG_03744"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[69392,70708],"is_not":false,"summary":null,"term":"GO:0008235"},{"annotations":[76156,99625,60601,64732,65526,57898,74324,116293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070006"},{"annotations":[76080,58368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004181"},{"annotations":[60938,61916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070573"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a peptide bond not more than three residues from the N- or C-terminus of a polypeptide chain by a mechanism in which water acts as a nucleophile, one or two metal ions hold the water molecule in place, and charged amino acid side chains are ligands for the metal ions.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metallopeptidase activity","termid":"GO:0008237"},{"relation_name":"is_a","term_name":"exopeptidase activity","termid":"GO:0008238"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_00451":null,"SJAG_00969":null,"SJAG_01088":null,"SJAG_01542":null,"SJAG_01896":null,"SJAG_02033":null,"SJAG_03009":null,"SJAG_03022":null,"SJAG_03586":null,"SJAG_03744":null,"SJAG_04103":null,"SJAG_04858":null,"SJAG_06636":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0140096","GO:0008233","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"metalloexopeptidase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0008235","terms_by_termid":{"GO:0004181":null,"GO:0008235":null,"GO:0070006":null,"GO:0070573":null}}


id: MONDO:0011979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Adult-onset foveomacular vitelliform dystrophy (AOFVD) is a genetic macular dystrophy characterized by blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated, yellow, egg yolk-like lesion located in the foveal or parafoveal region.","definition_xrefs":["Orphanet:99000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitelliform macular dystrophy","termid":"MONDO:0000390"}],"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":"adult-onset foveomacular vitelliform dystrophy","secondary_identifiers":["GARD:10909","MEDGEN:334280","SCTID:232049001","ICD10CM:H35.5","UMLS:C1842914","icd11.foundation:558806410"],"synonyms":[{"name":"AOFMD","type":"exact"},{"name":"AVMD","type":"exact"},{"name":"Gass disease","type":"exact"},{"name":"VMD3","type":"related"},{"name":"adult-onset foveomacular dystrophy","type":"exact"},{"name":"adult-onset foveomacular dystrophy with choroidal neovascularization","type":"exact"},{"name":"adult-onset vitelliform macular dystrophy","type":"exact"},{"name":"foveomacular dystrophy, adult-onset, with choroidal neovascularization","type":"related"},{"name":"foveomacular dystrophy, adult-onset; AOFMD","type":"related"},{"name":"macular dystrophy, vitelliform, 3","type":"related"},{"name":"macular dystrophy, vitelliform, adult-onset","type":"related"},{"name":"macular dystrophy, vitelliform, type 3","type":"exact"},{"name":"pseudo-Best disease","type":"exact"},{"name":"pseudo-vitelliform macular dystrophy","type":"exact"}],"termid":"MONDO:0011979","xrefs":{"Monarch":{"xref_id":"0011979"}}}


id: GO:0052334
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in the structure or function of the cytoskeleton of a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete modification by organism of cytoskeleton of other organism involved in symbiotic interaction (obsolete GO:0052334)","synonyms":[{"name":"modification by organism of cytoskeleton of other organism during symbiotic interaction","type":"related"}],"termid":"GO:0052334"}


id: FYPO:0003652
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription initiation from an RNA polymerase III promoter is abnormal.","definition_xrefs":["PomBase:mah","GO:0006384"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transcription during vegetative growth","termid":"FYPO:0004064"}],"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"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0006551","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal transcription initiation from RNA polymerase III promoter","synonyms":[{"name":"abnormal transcription initiation from RNA polymerase III promoter during mitotic cell cycle","type":"related"},{"name":"abnormal transcription initiation from RNA polymerase III promoter during vegetative growth","type":"exact"}],"termid":"FYPO:0003652"}


id: SO:0002314
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that alters the level or amount of gene product produced. This high level term can be applied where the direction of level change (increased vs decreased gene product level) is unknown or not confirmed.","definition_xrefs":["GenCC:AR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functional_effect_variant","termid":"SO:0001536"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"altered_gene_product_level","synonyms":[{"name":"altered gene product level","type":"exact"},{"name":"altered transcription level","type":"exact"},{"name":"altered_transcription_level","type":"exact"}],"termid":"SO:0002314"}


id: PBO:0085032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-canonical poly(A) polymerase; involved in nuclear RNA degradation as a component of the TRAMP complex; catalyzes polyadenylation of hypomodified tRNAs, and snoRNA and rRNA precursors; overlapping but non-redundant functions with Pap2p","termid":"PBO:0085032"}


id: GO:0039569
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the activity of host STAT2 (signal transducer and activator of transcription-2) by promoting the ubiquitin-dependent degradation of STAT2, mediated by the proteasome.","definition_xrefs":["PMID:19279106","PMID:11336548","PMID:17251292","VZ:257"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host STAT2 activity by positive regulation of STAT2 catabolic process (obsolete GO:0039569)","synonyms":[{"name":"promotion by virus of proteosome-dependent STAT2 degradation","type":"exact"},{"name":"suppression by virus of host STAT2 activity by positive promotion of STAT2 proteasome-mediated degradation","type":"exact"},{"name":"targeting STAT2 for proteasome-mediated degradation","type":"exact"}],"termid":"GO:0039569"}


id: FYPO:0001432
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of ethidium bromide than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002682","FYPO:0005447","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"resistance to ethidium bromide","synonyms":[{"name":"resistance to EtBr","type":"exact"},{"name":"resistance to ethidium bromide during mitotic cell cycle","type":"related"},{"name":"resistance to ethidium bromide during vegetative growth","type":"exact"},{"name":"resistant to ethidium bromide","type":"exact"}],"termid":"FYPO:0001432"}


id: PR:Q9P6J4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1683.06c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6J4"],"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 C1683.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1683.06c","synonyms":[{"name":"Spom972h-SPBC1683.06c","type":"exact"}],"termid":"PR:Q9P6J4"}


id: PBO:0057153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 301a","termid":"PBO:0057153"}


id: GO:0018183
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transient selenylation of peptidyl-cysteine to form S-selenyl-L-cysteine.","definition_xrefs":["RESID:AA0277"],"gene_count":0,"genotype_count":0,"name":"obsolete enzyme active site formation via S-selenyl-L-cysteine (obsolete GO:0018183)","synonyms":[{"name":"enzyme active site formation via S-selenyl-L-cysteine","type":"exact"}],"termid":"GO:0018183"}


id: PBO:0030178
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_3'-5'-exoribonuclease_activity","termid":"PBO:0030178"}


id: MONDO:0018395
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete male infertility due to sperm motility disorder (obsolete MONDO:0018395)","secondary_identifiers":["Orphanet:399813"],"synonyms":[{"name":"Male infertility due to asthenozoospermia","type":"exact"}],"termid":"MONDO:0018395","xrefs":{"Monarch":{"xref_id":"0018395"}}}


id: GO:0035220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Progression of the wing disc over time, from its initial formation through to its metamorphosis to form adult structures including the wing hinge, wing blade and pleura.","definition_xrefs":["ISBN:0879694238","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc development","termid":"GO:0007444"}],"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":"wing disc development","termid":"GO:0035220"}


id: GO:0003261
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a myocardial progenitor cell toward the midline to form the heart field. Cardiac muscle progenitor cells are non-terminally differentiated, mesoderm-derived cells that are committed to differentiate into myocardial cells of the heart.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardioblast migration to the midline involved in heart field formation","termid":"GO:0060975"}],"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":"cardiac muscle progenitor cell migration to the midline involved in heart field formation","synonyms":[{"name":"myocardial progenitor cell midline convergence","type":"exact"}],"termid":"GO:0003261"}


id: MONDO:0019789
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cytophagic histiocytic panniculitis (CHP) is a very rare form of panniculitis manifesting as recurrent multiple subcutaneous nodules (which may progressively become ecchymotic and ulcerated), and histologically characterized by lobular panniculitis with lymphocytic and histiocytic infiltration in the subcutaneous adipose tissue.","definition_xrefs":["Orphanet:94087"],"direct_ancestors":[{"relation_name":"is_a","term_name":"panniculitis","termid":"MONDO:0006591"},{"relation_name":"is_a","term_name":"subcutaneous tissue disorder","termid":"MONDO:0019296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytophagic histiocytic panniculitis","secondary_identifiers":["GARD:19249","SCTID:238883003","UMLS:C0406594","icd11.foundation:1978274002","MEDGEN:590528"],"synonyms":[{"name":"CHP","type":"exact"},{"name":"Winkelmann cytophagic panniculitis","type":"exact"}],"termid":"MONDO:0019789","xrefs":{"Monarch":{"xref_id":"0019789"}}}


id: PBO:0064743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 79","termid":"PBO:0064743"}


id: SO:0001034
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A de-branched intron which mimics the structure of pre-miRNA and enters the miRNA processing pathway without Drosha mediated cleavage.","definition_xrefs":["SO:ma","PMID:17589500"],"direct_ancestors":[{"relation_name":"has_part","term_name":"pre_miRNA","termid":"SO:0001244"},{"relation_name":"is_a","term_name":"intron_domain","termid":"SO:0001014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"miRtron","termid":"SO:0001034"}


id: MONDO:1010197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myositis ossificans that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myopathy, non-human animal","termid":"MONDO:1010195"},{"relation_name":"is_a","term_name":"inflammatory disease, non-human animal","termid":"MONDO:1011327"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myositis ossificans, non-human animal","secondary_identifiers":["OMIA:000697"],"termid":"MONDO:1010197","xrefs":{"Monarch":{"xref_id":"1010197"}}}


id: GO:0044728
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of adding or removing a methyl group from one or more nucleotides within an DNA molecule.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA methylation or demethylation (obsolete GO:0044728)","synonyms":[{"name":"changes in DNA methylation","type":"related"}],"termid":"GO:0044728"}


id: PBO:0108917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sSTAG3 cohesin complex component like 3 (pseudogene)","termid":"PBO:0108917"}


id: PBO:0030360
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_cellular_response_to_hypoxia","termid":"PBO:0030360"}


id: PBO:0041390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 5 open reading frame 58","termid":"PBO:0041390"}


id: MONDO:0001350
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the parametrium.","direct_ancestors":[{"relation_name":"is_a","term_name":"broad ligament malignant neoplasm","termid":"MONDO:0001108"}],"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":"parametrium malignant neoplasm","secondary_identifiers":["UMLS:C0153581","ICD10CM:C57.3","SCTID:448674007","MEDGEN:509332","DOID:11746","ICD9:183.4"],"synonyms":[{"name":"cancer of parametrium","type":"exact"},{"name":"malignant neoplasm of parametrium","type":"exact"},{"name":"malignant parametrium neoplasm","type":"exact"},{"name":"parametrium cancer","type":"exact"}],"termid":"MONDO:0001350","xrefs":{"Monarch":{"xref_id":"0001350"}}}


id: MONDO:1010637
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Factor XI deficiency that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"factor XI deficiency, non-human animal","termid":"MONDO:1010073"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"factor XI deficiency, domestic cat","secondary_identifiers":["OMIA:000363-9685"],"termid":"MONDO:1010637","xrefs":{"Monarch":{"xref_id":"1010637"}}}


id: PBO:0001038
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"promoter contains RLM1 element","termid":"PBO:0001038"}


id: GO:2000114
data:
  {"annotated_genes":["SJAG_03581","SJAG_00317","SJAG_04522","SJAG_02536","SJAG_01373","SJAG_03126","SJAG_00845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70750,96359],"is_not":false,"summary":null,"term":"GO:2000114"},{"annotations":[92731],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904846"},{"annotations":[114309,105494,109424],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061173"},{"annotations":[109425,118429],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000784"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of establishment of cell polarity.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of establishment or maintenance of cell polarity","termid":"GO:0032878"},{"relation_name":"regulates","term_name":"establishment of cell polarity","termid":"GO:0030010"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00317":null,"SJAG_00845":null,"SJAG_01373":null,"SJAG_02536":null,"SJAG_03126":null,"SJAG_03581":null,"SJAG_04522":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"regulation of establishment of cell polarity","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"regulation of bud site selection/establishment of cell polarity","type":"related"},{"name":"regulation of cell polarization","type":"exact"}],"termid":"GO:2000114","terms_by_termid":{"GO:0061173":null,"GO:1904846":null,"GO:2000114":null,"GO:2000784":null}}


id: GO:0003689
data:
  {"annotated_genes":["SJAG_00806","SJAG_02610","SJAG_02563","SJAG_00272","SJAG_00729","SJAG_00863","SJAG_02373","SJAG_01010","SJAG_02182","SJAG_04150"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70434,72802,74337,78159,78796,79484,93490,98100,114581,114672],"is_not":false,"summary":null,"term":"GO:0003689"}]},"cv_name":"molecular_function","definition":"Facilitating the opening of the ring structure of the PCNA complex, or any of the related sliding clamp complexes, and their closing around the DNA duplex, driven by ATP hydrolysis.","definition_xrefs":["GOC:vw","GOC:mah","PMID:16082778"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATP-dependent activity, acting on DNA","termid":"GO:0008094"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00272":null,"SJAG_00729":null,"SJAG_00806":null,"SJAG_00863":null,"SJAG_01010":null,"SJAG_02182":null,"SJAG_02373":null,"SJAG_02563":null,"SJAG_02610":null,"SJAG_04150":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0140097","GO:0003824"],"is_obsolete":false,"name":"DNA clamp loader activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0033170","Reactome:R-HSA-174439","Reactome:R-HSA-176264"],"synonyms":[{"name":"DNA clamp loading ATPase activity","type":"exact"},{"name":"DNA-protein loading ATPase activity","type":"related"},{"name":"PCNA loading activity","type":"narrow"},{"name":"PCNA loading complex activity","type":"narrow"},{"name":"protein-DNA loading ATPase activity","type":"related"}],"termid":"GO:0003689","terms_by_termid":{"GO:0003689":null}}


id: PBO:0005544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA export factor Rsm1","termid":"PBO:0005544"}


id: MONDO:0032721
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"}],"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":"spondyloepiphyseal dysplasia, kondo-fu type","secondary_identifiers":["NORD:2027","OMIM:618392","DOID:0112283","MEDGEN:1683128","UMLS:C5193071"],"synonyms":[{"name":"SEDKF","type":"related"},{"name":"SPONDYLOEPIPHYSEAL DYSPLASIA, KONDO-FU TYPE","type":"related"},{"name":"Sed With Elevated Blood Lysosomal Enzymes","type":"related"}],"termid":"MONDO:0032721","xrefs":{"Monarch":{"xref_id":"0032721"}}}


id: PBO:0048820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 5 pseudogene 4","termid":"PBO:0048820"}


id: MONDO:0015215
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A diaphragmatic or abdominal wall malformation that is not part of a larger syndrome.","definition_xrefs":["MONDO:patterns/isolated"],"gene_count":0,"genotype_count":0,"name":"obsolete non-syndromic diaphragmatic or abdominal wall malformation (obsolete MONDO:0015215)","secondary_identifiers":["Orphanet:108977"],"synonyms":[{"name":"isolated diaphragmatic or abdominal wall malformation","type":"exact"},{"name":"nonsyndromic diaphragmatic or abdominal wall malformation","type":"exact"}],"termid":"MONDO:0015215","xrefs":{"Monarch":{"xref_id":"0015215"}}}


id: GO:0048224
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An extracellular matrix part that consists of lignin in the form of a three-dimensional polymeric network. Lignins are complex racemic aromatic heteropolymers derived from a variety of phenylpropane monomers coupled together by an assortment of carbon-carbon and ether linkages. Lignin is crucial for structural integrity of the cell wall and stiffness and strength of the stem. In addition, lignin waterproofs the cell wall, enabling transport of water and solutes through the vascular system, and plays a role in protecting plants against pathogens.","definition_xrefs":["GOC:jid","PMID:16662709","GOC:mah","PMID:14503002"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"secondary cell wall","termid":"GO:0009531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005618"}],"interesting_parent_ids":["GO:0005575","GO:0005618"],"is_obsolete":false,"name":"lignin network","termid":"GO:0048224"}


id: MONDO:0020526
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute megakaryoblastic leukemia","termid":"MONDO:0018872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute megakaryoblastic leukemia in down syndrome","secondary_identifiers":["MEDGEN:1863778","Orphanet:99887","UMLS:C5925108","GARD:19697"],"synonyms":[{"name":"DS-AMKL","type":"exact"}],"termid":"MONDO:0020526","xrefs":{"Monarch":{"xref_id":"0020526"}}}


id: PBO:0090231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit Med9","termid":"PBO:0090231"}


id: GO:0000166
data:
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id: PBO:0064670
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 5","termid":"PBO:0064670"}


id: GO:0006167
data:
  {"annotated_genes":["SJAG_01859","SJAG_01070","SJAG_02850","SJAG_00044"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78671,80656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044208"},{"annotations":[75623,57284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044209"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of AMP, adenosine monophosphate.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide biosynthetic process","termid":"GO:0009152"},{"relation_name":"is_a","term_name":"purine ribonucleoside monophosphate biosynthetic process","termid":"GO:0009168"},{"relation_name":"is_a","term_name":"AMP metabolic process","termid":"GO:0046033"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_01070":null,"SJAG_01859":null,"SJAG_02850":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:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"AMP biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null},"synonyms":[{"name":"AMP anabolism","type":"exact"},{"name":"AMP biosynthesis","type":"exact"},{"name":"AMP formation","type":"exact"},{"name":"AMP synthesis","type":"exact"}],"termid":"GO:0006167","terms_by_termid":{"GO:0044208":null,"GO:0044209":null}}


id: FYPO:0000636
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a cell population in the vegetative growth phase of the life cycle grows at a faster rate than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell population growth","termid":"FYPO:0001356"},{"relation_name":"is_a","term_name":"increased cell population growth","termid":"FYPO:0003937"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002058","FYPO:0001985","FYPO:0005447","FYPO:0000003","FYPO:0002057"],"is_obsolete":false,"name":"increased cell population growth rate","synonyms":[{"name":"enhanced cell population growth","type":"related"},{"name":"fast cell population growth","type":"exact"},{"name":"increased cell population growth rate during mitotic cell cycle","type":"related"},{"name":"increased cell population growth rate during vegetative growth","type":"exact"},{"name":"increased cell population proliferation","type":"related"},{"name":"increased cell proliferation","type":"related"}],"termid":"FYPO:0000636"}


id: MONDO:0003591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant adipose tissue neoplasm of the fat cells surrounding the kidney, usually of the well-differentiated or myxoid type. It may be associated with tuberous sclerosis.","definition_xrefs":["NCIT:C6185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney sarcoma","termid":"MONDO:0002930"},{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005240"],"is_obsolete":false,"name":"kidney liposarcoma","secondary_identifiers":["UMLS:C1335745","MEDGEN:235546","DOID:5699"],"synonyms":[{"name":"kidney liposarcoma","type":"exact"},{"name":"liposarcoma of kidney","type":"exact"},{"name":"liposarcoma of the kidney","type":"exact"},{"name":"renal liposarcoma","type":"exact"}],"termid":"MONDO:0003591","xrefs":{"Monarch":{"xref_id":"0003591"}}}


id: GO:0052204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism stops, prevents, or reduces the frequency, rate or extent of the functional activity of proteins in a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of molecular function in other organism involved in symbiotic interaction (obsolete GO:0052204)","synonyms":[{"name":"down regulation of protein function in other organism during symbiotic interaction","type":"exact"},{"name":"down-regulation of protein function in other organism during symbiotic interaction","type":"exact"},{"name":"downregulation of protein function in other organism during symbiotic interaction","type":"exact"},{"name":"inhibition of protein function in other organism","type":"exact"},{"name":"inhibition of protein function in other organism during symbiotic interaction","type":"narrow"},{"name":"negative regulation of protein function in other organism during symbiotic interaction","type":"exact"}],"termid":"GO:0052204"}


id: GO:0018330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transient guanylylation of lysine to form N6-(phospho-5'-guanosine)-L-lysine, found in the guanylyltransferase active site of mRNA capping enzyme.","definition_xrefs":["RESID:AA0228"],"gene_count":0,"genotype_count":0,"name":"obsolete enzyme active site formation via N6-(phospho-5'-guanosine)-L-lysine (obsolete GO:0018330)","termid":"GO:0018330"}


id: FYPO:0001505
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 phosphatidylserine measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased phospholipid level","termid":"FYPO:0001288"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular phosphatidylserine level","synonyms":[{"name":"increased cellular PS level","type":"exact"},{"name":"increased cellular phosphatidyl-L-serine level","type":"exact"},{"name":"increased cellular phosphatidylserine level during mitotic cell cycle","type":"related"},{"name":"increased cellular phosphatidylserine level during vegetative growth","type":"exact"},{"name":"increased phosphatidylserine accumulation","type":"related"}],"termid":"FYPO:0001505"}


id: PBO:0039257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase 6 family member A1","termid":"PBO:0039257"}


id: GO:0046319
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of glucosylceramide.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucosylceramide biosynthetic process","termid":"GO:0046317"},{"relation_name":"is_a","term_name":"positive regulation of ceramide biosynthetic process","termid":"GO:2000304"},{"relation_name":"positively_regulates","term_name":"glucosylceramide biosynthetic process","termid":"GO:0006679"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"positive regulation of glucosylceramide biosynthetic process","synonyms":[{"name":"activation of glucosylceramide biosynthetic process","type":"narrow"},{"name":"positive regulation of glucosylceramide anabolism","type":"exact"},{"name":"positive regulation of glucosylceramide biosynthesis","type":"exact"},{"name":"positive regulation of glucosylceramide formation","type":"exact"},{"name":"positive regulation of glucosylceramide synthesis","type":"exact"},{"name":"stimulation of glucosylceramide biosynthetic process","type":"narrow"},{"name":"up regulation of glucosylceramide biosynthetic process","type":"exact"},{"name":"up-regulation of glucosylceramide biosynthetic process","type":"exact"},{"name":"upregulation of glucosylceramide biosynthetic process","type":"exact"}],"termid":"GO:0046319"}


id: PBO:0082081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-methylthioribose-1-phosphate isomerase; catalyzes the isomerization of 5-methylthioribose-1-phosphate to 5-methylthioribulose-1-phosphate in the methionine salvage pathway","termid":"PBO:0082081"}


id: PBO:0027354
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_pyruvate_decarboxylase_activity_during_stationary_phase","termid":"PBO:0027354"}


id: GO:0002067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a glandular epithelial cell. A glandular epithelial cell is a columnar/cuboidal epithelial cell found in a two dimensional sheet with a free surface exposed to the lumen of a gland.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"columnar/cuboidal epithelial cell differentiation","termid":"GO:0002065"}],"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":"glandular epithelial cell differentiation","termid":"GO:0002067"}


id: GO:0141033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or function of the host actin cytoskeleton by polymerizing the host filamentous actin. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:18331467","PMID:25293534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host actin cytoskeleton","termid":"GO:0141027"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host actin cytoskeleton via actin polymerization","synonyms":[{"name":"perturbation by symbiont of host actin cytoskeleton via actin polymerization","type":"exact"}],"termid":"GO:0141033"}


id: PBO:0029543
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_mixed_population,_vegetative_cells_with_abnormal_morphology,_including_long_cells_(obsolete_FYPO:0002179)","termid":"PBO:0029543"}


id: PBO:0080575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 3","termid":"PBO:0080575"}


id: MONDO:1010752
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypertrichosis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis, non-human animal","termid":"MONDO:1010130"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrichosis, dog","secondary_identifiers":["OMIA:000513-9615"],"termid":"MONDO:1010752","xrefs":{"Monarch":{"xref_id":"1010752"}}}


id: PBO:0029482
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_elongated_vegetative_cell_population_(obsolete_FYPO:0002233)","termid":"PBO:0029482"}


id: PBO:0063805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphorylase kinase regulatory subunit beta","termid":"PBO:0063805"}


id: PBO:0040373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase peripheral stalk subunit d pseudogene 1","termid":"PBO:0040373"}


id: PBO:0000418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prefoldin subunit 2 (predicted)","termid":"PBO:0000418"}


id: GO:1902662
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of peptidyl-L-cysteine S-palmitoylation.","definition_xrefs":["PMID:23444136","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein lipidation","termid":"GO:1903059"},{"relation_name":"regulates","term_name":"peptidyl-L-cysteine S-palmitoylation","termid":"GO:0018230"}],"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 peptidyl-L-cysteine S-palmitoylation","synonyms":[{"name":"regulation of peptidyl-S-palmitoyl-L-cysteine anabolism from peptidyl-cysteine","type":"exact"},{"name":"regulation of peptidyl-S-palmitoyl-L-cysteine biosynthetic process from peptidyl-cysteine","type":"exact"},{"name":"regulation of peptidyl-S-palmitoyl-L-cysteine formation from peptidyl-cysteine","type":"exact"},{"name":"regulation of peptidyl-S-palmitoyl-L-cysteine synthesis from peptidyl-cysteine","type":"exact"},{"name":"regulation of peptidyl-cysteine S-palmitoylation","type":"exact"}],"termid":"GO:1902662"}


id: PATO:0001139
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001139 urine glucose composition (obsolete PATO:0001139)","termid":"PATO:0001139"}


id: PBO:0042526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 3","termid":"PBO:0042526"}


id: PBO:0090188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar sorting protein Vps68","termid":"PBO:0090188"}


id: PBO:0053607
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 640","termid":"PBO:0053607"}


id: GO:0039618
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The protein coat that surrounds the infective nucleic acid in some virus particles where the subunits (capsomeres) are arranged to form an icosahedron with pseudo T=3 symmetry. The T=pseudo3 capsid is composed of 12 pentameric and 20 hexameric capsomeres.","definition_xrefs":["VZ:809"],"direct_ancestors":[{"relation_name":"is_a","term_name":"icosahedral viral capsid","termid":"GO:0019030"}],"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":"T=pseudo3 icosahedral viral capsid","termid":"GO:0039618"}


id: PBO:0083065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dihydrosphingosine 1-phosphate phosphatase; membrane protein involved in sphingolipid metabolism; YSR3 has a paralog, LCB3, that arose from the whole genome duplication","termid":"PBO:0083065"}


id: GO:0007165
data:
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id: GO:0050842
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The incorporation of copper into a protein by L-cysteinyl copper sulfido molybdopterin cytosine dinucleotide.","definition_xrefs":["RESID:AA0355"],"gene_count":0,"genotype_count":0,"name":"obsolete copper incorporation via L-cysteinyl copper sulfido molybdopterin cytosine dinucleotide (obsolete GO:0050842)","termid":"GO:0050842"}


id: MONDO:0013195
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNC1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"hypertrophic cardiomyopathy 13","secondary_identifiers":["DOID:0110319","MEDGEN:442487","MESH:C567686","OMIM:613243","UMLS:C2750472"],"synonyms":[{"name":"CMH13","type":"exact"},{"name":"TNNC1 hypertrophic cardiomyopathy","type":"exact"},{"name":"cardiomyopathy familial hypertrophic 13","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 13","type":"related"},{"name":"cardiomyopathy, familial hypertrophic, type 13","type":"exact"},{"name":"cardiomyopathy, hypertrophic, 13","type":"exact"},{"name":"hypertrophic cardiomyopathy caused by mutation in TNNC1","type":"exact"},{"name":"hypertrophic cardiomyopathy type 13","type":"exact"}],"termid":"MONDO:0013195","xrefs":{"Monarch":{"xref_id":"0013195"}}}


id: GO:0044485
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism initiates, promotes, or enhances fibrinogenolysis in another organism via the action of a venom. Fibrinogenolysis is the degradation of fibrinogen by proteolytic cleavage.","definition_xrefs":["GOC:fj","PMID:17433397","PMID:17544404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated depletion of circulating fibrinogen","termid":"GO:0044536"}],"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":"venom-mediated fibrinogenolysis","synonyms":[{"name":"envenomation resulting in fibrinogenolysis in another organism","type":"exact"},{"name":"envenomation resulting in fibrinogenolysis in other organism","type":"exact"}],"termid":"GO:0044485"}


id: MONDO:0005623
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammatory disease of the thyroid gland due to autoimmune responses leading to lymphocytic infiltration of the gland. It is characterized by the presence of circulating thyroid antigen-specific T-cells and thyroid autoantibodies. The clinical signs can range from hypothyroidism to thyrotoxicosis depending on the type of autoimmune thyroiditis.","definition_xrefs":["MESH:D013967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of endocrine system","termid":"MONDO:0000569"},{"relation_name":"is_a","term_name":"thyroiditis","termid":"MONDO:0004126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune thyroid disease","secondary_identifiers":["UMLS:C0920350","Wikipedia:Autoimmune_thyroiditis","MEDGEN:183088","EFO:0006812"],"synonyms":[{"name":"autoimmune thyroid gland inflammation","type":"exact"},{"name":"autoimmune thyroiditides","type":"related"},{"name":"autoimmune thyroiditis","type":"related"},{"name":"lymphocytic thyroiditides","type":"related"},{"name":"lymphocytic thyroiditis","type":"related"},{"name":"lymphomatous thyroiditides","type":"related"},{"name":"lymphomatous thyroiditis","type":"related"},{"name":"thyroiditides, autoimmune","type":"related"},{"name":"thyroiditides, lymphocytic","type":"related"},{"name":"thyroiditides, lymphomatous","type":"related"},{"name":"thyroiditis, lymphocytic","type":"related"},{"name":"thyroiditis, lymphomatous","type":"related"}],"termid":"MONDO:0005623","xrefs":{"Monarch":{"xref_id":"0005623"}}}


id: GO:0043483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of the pigment anthocyanin, contributing to anthocyanin accumulation in a tissue in response to a UV light stimulus.","definition_xrefs":["GOC:dph","GOC:jl","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anthocyanin-containing compound biosynthetic process","termid":"GO:0009718"},{"relation_name":"is_a","term_name":"pigment biosynthetic process involved in pigment accumulation","termid":"GO:0043477"},{"relation_name":"part_of","term_name":"anthocyanin accumulation in tissues in response to UV light","termid":"GO:0043481"}],"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":"anthocyanin biosynthetic process involved in anthocyanin accumulation in response to UV light","synonyms":[{"name":"anthocyanin biosynthesis during anthocyanin accumulation in tissues in response to UV light stimulus","type":"related"},{"name":"anthocyanin biosynthetic process during anthocyanin accumulation in response to UV light","type":"related"},{"name":"anthocyanin biosynthetic process during anthocyanin accumulation in tissues in response to UV light stimulus","type":"related"}],"termid":"GO:0043483"}


id: SO:0001419
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Intronic 2 bp region bordering exon. A splice_site that adjacent_to exon and overlaps intron.","definition_xrefs":["SO:ke","SO:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"splice_site","termid":"SO:0000162"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cis_splice_site","synonyms":[{"name":"cis splice site","type":"exact"}],"termid":"SO:0001419"}


id: GO:0021590
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for the cerebellum to attain its fully functional state. The cerebellum is the portion of the brain in the back of the head between the cerebrum and the pons. The cerebellum controls balance for walking and standing, modulates the force and range of movement and is involved in the learning of motor skills.","definition_xrefs":["GOC:dgh","GOC:dph","GOC:jid","ISBN:0838580343","GOC:cls","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure maturation","termid":"GO:0071695"},{"relation_name":"part_of","term_name":"cerebellum development","termid":"GO:0021549"},{"relation_name":"part_of","term_name":"hindbrain maturation","termid":"GO:0021578"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebellum maturation","termid":"GO:0021590"}


id: MONDO:0009596
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"metaphyseal chondrodysplasia","termid":"MONDO:0000138"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaphyseal chondrodysplasia, Pena type","secondary_identifiers":["OMIM:250300","UMLS:C1855195","MEDGEN:343289","MESH:C565399"],"synonyms":[{"name":"metaphyseal chondrodysplasia, Pena type","type":"exact"}],"termid":"MONDO:0009596","xrefs":{"Monarch":{"xref_id":"0009596"}}}


id: PBO:0001489
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choline kinase (predicted)","termid":"PBO:0001489"}


id: GO:0007207
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A phospholipase C-activating G protein-coupled receptor signaling pathway initiated by acetylcholine binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:tb","GOC:signaling","GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase C-activating G protein-coupled receptor signaling pathway","termid":"GO:0007200"},{"relation_name":"is_a","term_name":"G protein-coupled acetylcholine receptor signaling pathway","termid":"GO:0007213"}],"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":"phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway","synonyms":[{"name":"activation of phospholipase C activity by G-protein coupled acetylcholine receptor signaling pathway","type":"related"},{"name":"activation of phospholipase C activity by muscarinic acetylcholine receptor signaling pathway","type":"related"},{"name":"activation of phospholipase C activity by muscarinic acetylcholine receptor signalling pathway","type":"exact"},{"name":"muscarinic acetylcholine receptor, phospholipase C activating pathway","type":"related"},{"name":"muscarinic receptor signaling pathway via activation of PLC","type":"exact"},{"name":"phospholipase C-activating G-protein coupled acetylcholine receptor signaling pathway","type":"exact"}],"termid":"GO:0007207"}


id: PBO:0045986
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EI24 autophagy associated transmembrane protein","termid":"PBO:0045986"}


id: _global:symbiotically_interacts_with
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"A biotic interaction in which the two organisms live together in more or less intimate association.","direct_ancestors":[{"relation_name":"is_a","term_name":"participates_in_a_biotic-biotic_interaction_with","termid":"_global:participates_in_a_biotic-biotic_interaction_with"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"symbiotically_interacts_with","secondary_identifiers":["RO:0002440"],"termid":"_global:symbiotically_interacts_with"}


id: GO:1905935
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell fate determination.","definition_xrefs":["PMID:25793578","GOC:bhm","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of cell fate determination","termid":"GO:1905933"},{"relation_name":"positively_regulates","term_name":"cell fate determination","termid":"GO:0001709"}],"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 cell fate determination","synonyms":[{"name":"activation of cell fate determination","type":"narrow"},{"name":"up regulation of cell fate determination","type":"exact"},{"name":"up-regulation of cell fate determination","type":"exact"},{"name":"upregulation of cell fate determination","type":"exact"}],"termid":"GO:1905935"}


id: MONDO:0044663
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aquagenic syringeal acrokeratoderma is a rare condition affecting the palms of the hands. It is characterized by the appearance or worsening of a palmar eruption, following brief exposure to water. The palmar eruption is made up of small, white or shining pimples that can conjoin into plaques. The feet are unaffected. Symptoms include a burning pain and a tightening sensation in the palms, as well as too much sweating. There are two variants. Most commonly, it is a temporary and recurrent condition that appears after submersion in water, known as the bhand in the bucket sign,b that gets better within minutes to hours of drying. A less common variant is characterized by persistent lesions that are worsened after water submersion. The cause of aquagenic syringeal acrokeratoderma is unknown, but likely relates to sweating. Several studies have found that it is present in about 40% to 84% of cystic fibrosis patients and also in carriers, which suggest that it may be caused by mutations in the CFTR gene. It is more often found in young women. Besides cystic fibrosis, it is also seen in wasting (marasmus) and nephrotic syndrome and also with the use of aspirin and other drugs such as rofecoxib and celecoxib. In most cases it does not need any treatment and resolves spontaneously. When necessary, it can be treated with topical aluminum chloride or salicylic acid ointment or with tap water iontophoresis.","definition_xrefs":["GARD:0012991"],"direct_ancestors":[{"relation_name":"is_a","term_name":"palmoplantar keratosis","termid":"MONDO:0006590"},{"relation_name":"is_a","term_name":"epidermal disease","termid":"MONDO:0019268"}],"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":"aquagenic palmoplantar keratoderma","secondary_identifiers":["Orphanet:498359","MEDGEN:1789947","GARD:12991","UMLS:C4087301"],"synonyms":[{"name":"Transient reactive papulotranslucent acrokeratoderma","type":"related"},{"name":"aquagenic keratoderma","type":"exact"},{"name":"aquagenic palmoplantar keratoderma","type":"exact"},{"name":"aquagenic syringeal acrokeratoderma","type":"exact"},{"name":"aquagenic wrinkling of the hands","type":"related"},{"name":"aquagenic wrinkling of the palms","type":"exact"},{"name":"transient reactive papulotranslucent acrokeratoderma","type":"exact"}],"termid":"MONDO:0044663","xrefs":{"Monarch":{"xref_id":"0044663"}}}


id: PBO:0028269
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_nitric_oxide_level_during_cellular_response_to_cadmium_ion","termid":"PBO:0028269"}


id: GO:0071278
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 cesium stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cesium ion","termid":"GO:0010164"},{"relation_name":"is_a","term_name":"cellular response to metal ion","termid":"GO:0071248"}],"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 cesium ion","synonyms":[{"name":"cellular response to cesium","type":"exact"}],"termid":"GO:0071278"}


id: MONDO:0018420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"autosomal recessive spastic paraplegia type 68","secondary_identifiers":["Orphanet:401825"],"synonyms":[{"name":"SPG68","type":"exact"}],"termid":"MONDO:0018420","xrefs":{"Monarch":{"xref_id":"0018420"}}}


id: GO:0018072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-glutamic acid residues by the covalent attachment of ethanolamine, itself further modified by the addition of a phosphoglycerol unit.","definition_xrefs":["PMID:2569467","RESID:AA0170"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-L-glutamyl 5-glycerylphosphorylethanolamine biosynthetic process from peptidyl-glutamic acid (obsolete GO:0018072)","synonyms":[{"name":"peptidyl-L-glutamyl 5-glycerylphosphorylethanolamine anabolism from peptidyl-glutamic acid","type":"exact"},{"name":"peptidyl-L-glutamyl 5-glycerylphosphorylethanolamine formation from peptidyl-glutamic acid","type":"exact"},{"name":"peptidyl-L-glutamyl 5-glycerylphosphorylethanolamine synthesis from peptidyl-glutamic acid","type":"exact"}],"termid":"GO:0018072"}


id: PBO:0062191
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 Q member 3","termid":"PBO:0062191"}


id: GO:0060088
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a stereocilium. A stereocilium is an actin-based protrusion from the apical surface of auditory hair cells.","definition_xrefs":["PMID:10978835","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner ear receptor cell stereocilium organization","termid":"GO:0060122"},{"relation_name":"part_of","term_name":"auditory receptor cell morphogenesis","termid":"GO:0002093"}],"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":"auditory receptor cell stereocilium organization","synonyms":[{"name":"auditory receptor cell stereocilium organisation","type":"exact"},{"name":"auditory receptor cell stereocilium organization and biogenesis","type":"related"}],"termid":"GO:0060088"}


id: GO:0016361
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with activin-bound type II activin receptor to initiate a change in cell activity; upon binding, acts as a downstream transducer of activin signals.","definition_xrefs":["GOC:mah","PMID:8622651"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activin receptor activity","termid":"GO:0017002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0004672"}],"interesting_parent_ids":["GO:0004672","GO:0016301","GO:0038023","GO:0140096","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"activin receptor activity, type I","synonyms":[{"name":"type I activin receptor activity","type":"exact"}],"termid":"GO:0016361"}


id: MONDO:0044753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A spinal stenosis that involves the lumbar region of vertebral column.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spinal stenosis","termid":"MONDO:0005965"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lumbar spinal stenosis","secondary_identifiers":["UMLS:C0158288","HP:0004610","ICD9:724.02","SCTID:18347007","NCIT:C177445","MEDGEN:488791"],"synonyms":[{"name":"lumbar region of vertebral column spinal stenosis","type":"exact"},{"name":"lumbar spinal stenosis","type":"exact"},{"name":"spinal stenosis of lumbar region","type":"exact"},{"name":"spinal stenosis of lumbar region of vertebral column","type":"exact"}],"termid":"MONDO:0044753","xrefs":{"Monarch":{"xref_id":"0044753"}}}


id: FYECO:0000051
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which linolenic acid was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ fatty acid","termid":"FYECO:0000042"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ linolenic acid","termid":"FYECO:0000051"}


id: PBO:0089845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3 beta-hydroxysteroid dehydrogenase/delta 5-->4-isomerase Erg26","termid":"PBO:0089845"}


id: MONDO:0009018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Central cloudy dystrophy of François is a very rare form of stromal corneal dystrophy characterized by polygonal or rounded stromal opacities surrounded by clear tissue, and generally no effect on vision.","definition_xrefs":["Orphanet:98972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stromal corneal dystrophy","termid":"MONDO:0020213"},{"relation_name":"is_a","term_name":"posterior corneal dystrophy","termid":"MONDO:0020214"}],"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":"central cloudy dystrophy of François","secondary_identifiers":["SCTID:419074008","UMLS:C1622427","MEDGEN:302006","GARD:16881","MESH:C563262","OMIM:217600"],"synonyms":[{"name":"CCDF","type":"exact"},{"name":"central cloudy corneal dystrophy of François","type":"exact"},{"name":"central cloudy dystrophy of Francois","type":"exact"},{"name":"central cloudy dystrophy of François","type":"exact"},{"name":"corneal dystrophy, central type","type":"related"}],"termid":"MONDO:0009018","xrefs":{"Monarch":{"xref_id":"0009018"}}}


id: PBO:0051757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol polyphosphate multikinase pseudogene 1","termid":"PBO:0051757"}


id: GO:0005184
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action characteristic of a neuropeptide hormone, any peptide hormone that acts in the central nervous system. A neuropeptide is any of several types of molecules found in brain tissue, composed of short chains of amino acids; they include endorphins, enkephalins, vasopressin, and others. They are often localized in axon terminals at synapses and are classified as putative neurotransmitters, although some are also hormones.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone activity","termid":"GO:0005179"},{"relation_name":"is_a","term_name":"neuropeptide activity","termid":"GO:0160041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0140677","GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"neuropeptide hormone activity","secondary_identifiers":["Wikipedia:Neurohormone"],"synonyms":[{"name":"neurohormone","type":"exact"}],"termid":"GO:0005184"}


id: PBO:0072187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S17 pseudogene 3","termid":"PBO:0072187"}


id: PR:Q10174
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC27F1.05c gene.","definition_xrefs":["UniProtKB:Q10174","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 aminotransferase C27F1.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC27F1.05c","synonyms":[{"name":"Spom972h-SPAC27F1.05c","type":"exact"}],"termid":"PR:Q10174"}


id: MONDO:0020159
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":"congenital entropion","secondary_identifiers":["MedDRA:10014923","MEDGEN:540011","SCTID:20392000","UMLS:C0266579","Orphanet:98568","ICD10CM:Q10.2"],"termid":"MONDO:0020159","xrefs":{"Monarch":{"xref_id":"0020159"}}}


id: MONDO:0009660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme beta galactosidase. It is characterized by skeletal dysplasia and short stature.","definition_xrefs":["NCIT:C84902"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis type 4","termid":"MONDO:0018938"},{"relation_name":"is_a","term_name":"lysosomal storage disease with skeletal involvement","termid":"MONDO:0800088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"mucopolysaccharidosis type 4B","secondary_identifiers":["SCTID:238044004","ICD10CM:E76.211","OMIM:253010","UMLS:C0086652","MEDGEN:43376","icd11.foundation:1479415032","NANDO:1200107","NANDO:2201179","DOID:0111392","Orphanet:309310","GARD:3786"],"synonyms":[{"name":"Beta-D-galactosidase deficiency","type":"exact"},{"name":"MPS 4B","type":"exact"},{"name":"MPS IV B","type":"exact"},{"name":"MPS IVB","type":"related"},{"name":"MPS4B","type":"exact"},{"name":"MPSIVB","type":"exact"},{"name":"Morquio disease type B","type":"exact"},{"name":"Morquio syndrome B","type":"exact"},{"name":"mucopolysaccharidosis type IVB","type":"exact"},{"name":"mucopolysaccharidosis type IVB (Morquio)","type":"exact"},{"name":"mucopolysaccharidosis, type 4B","type":"related"},{"name":"mucopolysaccharidosis, type IVB","type":"related"}],"termid":"MONDO:0009660","xrefs":{"Monarch":{"xref_id":"0009660"}}}


id: PR:Q09893
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC24B11.05 gene.","definition_xrefs":["UniProtKB:Q09893","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 C24B11.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24B11.05","synonyms":[{"name":"Spom972h-SPAC24B11.05","type":"exact"}],"termid":"PR:Q09893"}


id: FYPO:0002268
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which glutamate-ammonia ligase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished catalytic activity","termid":"FYPO:0000664"},{"relation_name":"is_a","term_name":"abnormal glutamate-ammonia ligase activity","termid":"FYPO:0002267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"abolished glutamate-ammonia ligase activity","synonyms":[{"name":"abolished GS activity","type":"exact"},{"name":"abolished glutamine synthetase activity","type":"exact"},{"name":"abolished glutamylhydroxamic synthetase activity","type":"exact"},{"name":"glutamate-ammonia ligase activity abolished","type":"exact"}],"termid":"FYPO:0002268"}


id: PR:O42870
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phenylalanine--tRNA ligase alpha subunit that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01327","PRO:DNx","PANTHER:PTHR11538:SF15"],"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":"phenylalanine--tRNA ligase alpha subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3G9.06","secondary_identifiers":["UniProtKB:O42870"],"synonyms":[{"name":"PheRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-FARSA","type":"exact"},{"name":"phenylalanyl-tRNA synthetase alpha subunit (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42870"}


id: PBO:0045093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal-less homeobox 4","termid":"PBO:0045093"}


id: PBO:0050927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon induced transmembrane protein 4 pseudogene","termid":"PBO:0050927"}


id: GO:0102744
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + 2-trans,6-trans,10-trans-geranylgeranyl diphosphate + NADPH = dihydrogeranylgeranyl-PP + NADP.","definition_xrefs":["GOC:pz","EC:1.3.1.-"],"gene_count":0,"genotype_count":0,"name":"obsolete all-trans-geranyl-geranyl diphosphate reductase activity (obsolete GO:0102744)","termid":"GO:0102744"}


id: PBO:0002964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNF2 family helicase Ino80","termid":"PBO:0002964"}


id: PBO:0050496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox B6","termid":"PBO:0050496"}


id: MOD:01981
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form 3-methyllanthionine with unresolved stereospecificity.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"beta-carbon thioether crosslinked residues","termid":"MOD:01993"},{"relation_name":"is_a","term_name":"crosslinked L-threonine residue","termid":"MOD:02056"}],"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":"3-methyllanthionine","synonyms":[{"name":"2,6-diamino-3-methyl-4-thiaheptanedioic acid","type":"exact"},{"name":"2-amino-3-([2-amino-2-carboxyethyl]sulfanyl)butanoic acid","type":"exact"},{"name":"2-amino-3-[(2-amino-2-carboxyethyl)thio]butanoic acid","type":"exact"},{"name":"2-azanyl-3-[(2-azanyl-2-carboxyethyl)sulfanyl]butanoic acid","type":"exact"},{"name":"3-methyllanthionine","type":"exact"},{"name":"cysteine-3-L-butyrine thioether","type":"exact"}],"termid":"MOD:01981"}


id: PBO:0067981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 283","termid":"PBO:0067981"}


id: GO:0032971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of muscle filament sliding.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle contraction","termid":"GO:0006937"},{"relation_name":"is_a","term_name":"regulation of intracellular transport","termid":"GO:0032386"},{"relation_name":"is_a","term_name":"regulation of actin filament-based movement","termid":"GO:1903115"},{"relation_name":"regulates","term_name":"muscle filament sliding","termid":"GO:0030049"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of muscle filament sliding","termid":"GO:0032971"}


id: PBO:0030493
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-coenzyme_Q10_absent_from_cell","termid":"PBO:0030493"}


id: GO:0070873
data:
  {"annotated_genes":["SJAG_00963","SJAG_01376"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80716,78783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045719"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving glycogen.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polysaccharide metabolic process","termid":"GO:0032881"},{"relation_name":"is_a","term_name":"regulation of generation of precursor metabolites and energy","termid":"GO:0043467"},{"relation_name":"regulates","term_name":"glycogen metabolic process","termid":"GO:0005977"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00963":null,"SJAG_01376":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0006091"],"is_obsolete":false,"name":"regulation of glycogen metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"regulation of glycogen metabolism","type":"exact"}],"termid":"GO:0070873","terms_by_termid":{"GO:0045719":null}}


id: FYPO:0002281
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a germ tube with abnormal size, shape, or structure.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination","termid":"FYPO:0000316"},{"relation_name":"is_a","term_name":"inviable vegetative cell with abnormal cell morphology","termid":"FYPO:0002273"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000004","FYPO:0000005","FYPO:0000002"],"is_obsolete":false,"name":"inviable after spore germination with abnormal germ tube morphology","synonyms":[{"name":"inviable following spore germination with abnormal germ tube morphology","type":"exact"},{"name":"inviable germinated spore with abnormal germ tube morphology","type":"exact"},{"name":"lethal after spore germination with abnormal germ tube morphology","type":"exact"}],"termid":"FYPO:0002281"}


id: PBO:0049783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 18","termid":"PBO:0049783"}


id: PBO:0076957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transforming growth factor beta induced","termid":"PBO:0076957"}


id: PBO:0045251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal light chain 1","termid":"PBO:0045251"}


id: MONDO:0022464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete anophthalmia microcephaly hypogonadism (obsolete MONDO:0022464)","termid":"MONDO:0022464","xrefs":{"Monarch":{"xref_id":"0022464"}}}


id: PR:Q09948
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rsc4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09948"],"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":"chromatin structure-remodeling complex subunit rsc4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1734.15","synonyms":[{"name":"RSC complex subunit rsc4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rsc4","type":"exact"},{"name":"bromodomain-containing protein brd1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09948"}


id: GO:0099107
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Modulation of the activity of an ion channel via direct interaction with it as part of G protein-coupled receptor signaling.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete ion channel regulator activity involved in G protein-coupled receptor signaling pathway (obsolete GO:0099107)","synonyms":[{"name":"ion channel regulator activity involved in G-protein coupled receptor signaling pathway","type":"exact"}],"termid":"GO:0099107"}


id: GO:0075346
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism adds one or more ubiquitin groups to a protein of 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 modification by symbiont of host protein by ubiquitination (obsolete GO:0075346)","synonyms":[{"name":"modification by symbiont of host protein by ubiquitinylation","type":"exact"},{"name":"modification by symbiont of host protein by ubiquitylation","type":"exact"}],"termid":"GO:0075346"}


id: PBO:0005202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-type ATPase P5 type (predicted)","termid":"PBO:0005202"}


id: FYPO:0000547
data:
  {"alleles_by_uniquename":{"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121213],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001038"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of protein modification is increased. All modifications may be affected, or only modifications of a certain type, or on specific proteins, or even specific sites within specific proteins.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification during vegetative growth","termid":"FYPO:0000329"},{"relation_name":"is_a","term_name":"increased protein modification","termid":"FYPO:0002499"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01787":null,"SJAG_04551":null},"genotype_count":1,"genotypes_by_uniquename":{"pck1delta":{"display_name":"pck1delta","display_uniquename":"pck1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0002494","FYPO:0002274"],"is_obsolete":false,"name":"increased protein modification during vegetative growth","references_by_uniquename":{"PMID:34198697":null},"single_locus_annotated_genes":["SJAG_01787"],"single_locus_genotype_uniquenames":["pck1delta"],"synonyms":[{"name":"increased protein modification during mitotic cell cycle","type":"related"},{"name":"increased protein/peptide modification during vegetative growth","type":"exact"}],"termid":"FYPO:0000547","terms_by_termid":{"FYPO:0001038":null}}


id: MONDO:0003717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A papillary tumor originating in the renal pelvis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary urothelial neoplasm","termid":"MONDO:0003443"},{"relation_name":"is_a","term_name":"renal pelvis neoplasm","termid":"MONDO:0003719"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal pelvis papillary tumor","secondary_identifiers":["MEDGEN:163120","NCIT:C8603","UMLS:C0853688","DOID:5975"],"synonyms":[{"name":"papillary neoplasm of renal pelvis","type":"exact"},{"name":"papillary neoplasm of the renal pelvis","type":"exact"},{"name":"papillary tumor of renal pelvis","type":"exact"},{"name":"papillary tumor of the renal pelvis","type":"exact"},{"name":"papillary tumour of renal pelvis","type":"exact"},{"name":"papillary tumour of the renal pelvis","type":"exact"},{"name":"renal pelvis papillary tumor","type":"exact"},{"name":"renal pelvis papillary urothelial neoplasm","type":"exact"}],"termid":"MONDO:0003717","xrefs":{"Monarch":{"xref_id":"0003717"}}}


id: PBO:0054067
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 1414","termid":"PBO:0054067"}


id: MONDO:0017404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal Xq28 microduplication syndrome is a rare, hereditary, syndromic intellectual disability characterized by cognitive impairment, behavioral and psychiatric problems, recurrent infections, atopic diseases, and distinctive facial features in males. Females are clinically asymptomatic or mildly affected, presenting mild learning difficulties and facial dysmorphism.","definition_xrefs":["Orphanet:293939"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"chromosome Xq28 duplication syndrome","termid":"MONDO:0010436"}],"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":"distal Xq28 microduplication syndrome","secondary_identifiers":["GARD:17350","UMLS:C4751127","DECIPHER:88","MEDGEN:1655645"],"synonyms":[{"name":"Xq28 Microduplication","type":"exact"},{"name":"distal dup(X)q(28)","type":"exact"},{"name":"distal trisomy Xq28","type":"exact"}],"termid":"MONDO:0017404","xrefs":{"Monarch":{"xref_id":"0017404"}}}


id: PBO:0113314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in recycling of membrane transporters from endosome to plasma membrane; plays a role in the multivesicular body sorting pathway; functions and forms a complex with Did2p; recruitment to endosomes is mediated by the Vps2p-Vps24p subcomplex of ESCRT-III; also interacts with Vps4p","termid":"PBO:0113314"}


id: SO:0001129
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Left handed type I (dihedral angles):- Residue(i): -140 degrees < chi (1) -120 degrees < -20 degrees, -90 degrees < psi +120 degrees < +40 degrees. Residue(i+1): -140 degrees < phi < -20 degrees, -90 degrees < psi < +40 degrees.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asx_turn","termid":"SO:0000912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"asx_turn_left_handed_type_one","secondary_identifiers":["BS:00206"],"synonyms":[{"name":"asx turn left handed type one","type":"exact"},{"name":"asx_turn_il","type":"related"}],"termid":"SO:0001129"}


id: PBO:0003116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EH domains","termid":"PBO:0003116"}


id: GO:0017017
data:
  {"annotated_genes":["SJAG_03263"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72756],"is_not":false,"summary":null,"term":"GO:0017017"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: MAP kinase serine/threonine/tyrosine phosphate + H2O = MAP kinase serine/threonine/tyrosine + phosphate.","definition_xrefs":["PMID:12184814","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein tyrosine/serine/threonine phosphatase activity","termid":"GO:0008138"},{"relation_name":"is_a","term_name":"MAP kinase phosphatase activity","termid":"GO:0033549"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03263":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016788","GO:0140096","GO:0016787","GO:0004721"],"is_obsolete":false,"name":"MAP kinase tyrosine/serine/threonine phosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"dual-specificity MAP kinase phosphatase activity","type":"exact"}],"termid":"GO:0017017","terms_by_termid":{"GO:0017017":null}}


id: FYPO:0000118
data:
  {"alleles_by_uniquename":{"SJAG_00118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00118","name":"mid2delta","uniquename":"SJAG_00118:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121066],"is_not":false,"summary":null,"term":"FYPO:0000118"}],"single_locus_phenotype":[{"annotations":[121055,121056],"is_not":false,"summary":null,"term":"FYPO:0000118"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle characterized by the presence of more than one septum in a cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"septated vegetative cell","termid":"FYPO:0002342"},{"relation_name":"is_a","term_name":"multiseptate cell","termid":"FYPO:0004295"},{"relation_name":"output_of","term_name":"abnormal cytokinesis during vegetative growth","termid":"FYPO:0000032"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00118":null,"SJAG_01143":null},"genotype_count":3,"genotypes_by_uniquename":{"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__mid2delta":{"display_name":"mid1delta mid2delta","display_uniquename":"mid1delta__mid2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_00118:allele-1","expression":"Null"}]}]},"mid2delta":{"display_name":"mid2delta","display_uniquename":"mid2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00118:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0000631","FYPO:0000032"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_00118","SJAG_01143"],"name":"multiseptate vegetative cell","references_by_uniquename":{"PMID:25866389":null},"single_locus_annotated_genes":["SJAG_01143","SJAG_00118"],"single_locus_genotype_uniquenames":["mid2delta","mid1delta"],"synonyms":[{"name":"multiseptate during mitotic cell cycle","type":"related"},{"name":"multiseptate during vegetative growth","type":"exact"},{"name":"septation defects, multiple septa during vegetative growth","type":"exact"}],"termid":"FYPO:0000118","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000118":null}}


id: MONDO:0010752
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"VACTERL/vater association","termid":"MONDO:0008642"},{"relation_name":"is_a","term_name":"VACTERL with hydrocephalus","termid":"MONDO:0010172"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VACTERL association, X-linked, with or without hydrocephalus","secondary_identifiers":["GARD:15309","UMLS:C2931228","MEDGEN:419019","OMIM:314390","DOID:0111766"],"synonyms":[{"name":"VACTERL association with hydrocephaly, X-linked","type":"related"},{"name":"VACTERL association, X-linked, X-linked recessive","type":"exact"},{"name":"VACTERL association, X-linked, with or without hydrocephalus","type":"exact"},{"name":"VACTERL-H, X-linked","type":"related"},{"name":"VACTERLX","type":"related"},{"name":"X-linked VACTERL-H syndrome","type":"related"}],"termid":"MONDO:0010752","xrefs":{"Monarch":{"xref_id":"0010752"}}}


id: FYPO:0005995
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 mature long non-coding RNA (lncRNA) measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased ncRNA level during vegetative growth","termid":"FYPO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0006551","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased lncRNA level","synonyms":[{"name":"increased lncRNA accumulation","type":"related"},{"name":"increased lncRNA level during mitotic cell cycle","type":"related"},{"name":"increased lncRNA level during vegetative growth","type":"exact"},{"name":"increased lncRNA transcript level","type":"broad"},{"name":"increased long non-coding RNA level","type":"exact"},{"name":"increased mature lncRNA level","type":"exact"}],"termid":"FYPO:0005995"}


id: PBO:0052867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 5-10","termid":"PBO:0052867"}


id: PBO:0080257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 20 pseudogene","termid":"PBO:0080257"}


id: PBO:0066925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 227","termid":"PBO:0066925"}


id: MONDO:0005601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive adenocarcinoma that arises from the ovary and is characterized by the presence of malignant epithelial cells that contain intracytoplasmic mucin. There is cellular atypia, increased layering of cells, complexity of glands, and papillary formations.","definition_xrefs":["NCIT:C5243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian adenocarcinoma","termid":"MONDO:0002752"},{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"},{"relation_name":"is_a","term_name":"mucinous ovarian cancer","termid":"MONDO:0024282"}],"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":"ovarian mucinous adenocarcinoma","secondary_identifiers":["Orphanet:398961","UMLS:C1335167","DOID:3606","GARD:21651","icd11.foundation:869438441","EFO:0006462","MEDGEN:235418"],"synonyms":[{"name":"mucinous adenocarcinoma of ovary","type":"exact"},{"name":"mucinous adenocarcinoma of the ovary","type":"exact"},{"name":"mucinous carcinoma of ovary","type":"exact"},{"name":"mucinous carcinoma of the ovary","type":"exact"},{"name":"ovarian mucinous adenocarcinoma","type":"exact"},{"name":"ovarian mucinous carcinoma","type":"exact"},{"name":"ovary mucinous adenocarcinoma","type":"exact"}],"termid":"MONDO:0005601","xrefs":{"Monarch":{"xref_id":"0005601"}}}


id: GO:0021770
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the parahippocampal gyrus over time from its initial formation until its mature state. The parahippocampal gyrus is a ridge in the cerebral cortex.","definition_xrefs":["GOC:jid","GO_REF:0000021","ISBN:0878937420","GOC:cls","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"limbic system development","termid":"GO:0021761"}],"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":"parahippocampal gyrus development","secondary_identifiers":["Wikipedia:parahippocampal_gyrus"],"synonyms":[{"name":"hippocampal gyrus development","type":"exact"}],"termid":"GO:0021770"}


id: FYPO:0003080
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 genetic imprinting at the mating-type locus does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal genetic imprinting at mating-type locus","termid":"FYPO:0003079"},{"relation_name":"is_a","term_name":"abolished biological process","termid":"FYPO:0005448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0000293","FYPO:0001985"],"is_obsolete":false,"name":"abolished genetic imprinting at mating-type locus","synonyms":[{"name":"abolished genetic imprinting at mating-type locus during mitotic cell cycle","type":"related"},{"name":"genetic imprinting at mating-type locus abolished","type":"exact"},{"name":"genetic imprinting at mating-type locus abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0003080"}


id: PBO:0027039
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_mitotically_up-regulated_gene_mRNA_during_vegetative_growth","termid":"PBO:0027039"}


id: PBO:0074636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 30","termid":"PBO:0074636"}


id: PBO:0044310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b5 reductase like","termid":"PBO:0044310"}


id: GO:0030531
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A complex composed of RNA of the small cytoplasmic RNA (scRNA) class and protein, found in the cytoplasm.","definition_xrefs":["GOC:mah","GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete small cytoplasmic ribonucleoprotein complex (obsolete GO:0030531)","synonyms":[{"name":"scRNP","type":"exact"},{"name":"small cytoplasmic ribonucleoprotein","type":"exact"},{"name":"small cytoplasmic ribonucleoprotein complex","type":"exact"}],"termid":"GO:0030531"}


id: GO:0097119
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The clustering process in which postsynaptic density protein 95 (PSD-95) molecules are localized to distinct domains in the cell membrane. PSD-95 is mostly located in the post synaptic density of neurons, and is involved in anchoring synaptic proteins.","definition_xrefs":["GOC:BHF","GOC:sjp","PMID:10433269"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to membrane","termid":"GO:0072657"},{"relation_name":"part_of","term_name":"postsynaptic membrane organization","termid":"GO:0001941"},{"relation_name":"part_of","term_name":"postsynaptic density organization","termid":"GO:0097106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0061024"],"is_obsolete":false,"name":"postsynaptic density protein 95 clustering","synonyms":[{"name":"Dlg4 clustering","type":"exact"},{"name":"PSD-95 clustering","type":"exact"},{"name":"post-synaptic density protein 95 clustering","type":"exact"}],"termid":"GO:0097119"}


id: GO:1903603
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of thermospermine.","definition_xrefs":["PMID:24906355","GOC:TermGenie","GO_REF:0000068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine biosynthetic process","termid":"GO:0006596"},{"relation_name":"is_a","term_name":"thermospermine metabolic process","termid":"GO:1903601"}],"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":"thermospermine biosynthetic process","synonyms":[{"name":"thermospermine anabolism","type":"exact"},{"name":"thermospermine biosynthesis","type":"exact"},{"name":"thermospermine formation","type":"exact"},{"name":"thermospermine synthesis","type":"exact"}],"termid":"GO:1903603"}


id: GO:0045458
data:
  {"annotated_genes":["SJAG_04816"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106222],"is_not":false,"summary":null,"term":"GO:0045458"}]},"cv_name":"biological_process","definition":"Genetic recombination within the DNA of the genes coding for ribosomal RNA.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA recombination","termid":"GO:0006310"},{"relation_name":"is_a","term_name":"maintenance of rDNA","termid":"GO:0043007"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04816":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0006310","GO:0008150"],"is_obsolete":false,"name":"recombination within rDNA repeats","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"recombination within ribosomal DNA repeats","type":"exact"}],"termid":"GO:0045458","terms_by_termid":{"GO:0045458":null}}


id: PBO:0031588
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_biofilm_formation","termid":"PBO:0031588"}


id: MONDO:0034820
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability characterized by unilateral or bilateral cleft lip and palate and craniofacial dysmorphism (including frontal bossing, hypertelorism, broad flat nasal bridge, cupped ears/thickened helices, and micrognathia). Additional manifestations are variable congenital cardiac anomalies, pectus excavatum, abnormalities of the hands and feet, ocular abnormalities (myopia, cataract, staphyloma), and conductive or sensorineural hearing loss.","definition_xrefs":["Orphanet:508476"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome","secondary_identifiers":["MEDGEN:1800190","UMLS:C5568767","GARD:22068"],"synonyms":[{"name":"cleft lip and palate-craniofacial dysmorphism-congenital heart defect-deafness syndrome","type":"exact"},{"name":"hyaluronidase 2 deficiency","type":"exact"}],"termid":"MONDO:0034820","xrefs":{"Monarch":{"xref_id":"0034820"}}}


id: PBO:0039375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiomotin","termid":"PBO:0039375"}


id: PBO:0069125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 375, pseudogene","termid":"PBO:0069125"}


id: MONDO:0010939
data:
  {"annotated_genes":["SJAG_03363"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87081],"is_not":false,"summary":null,"term":"MONDO:0010939"}]},"cv_name":"mondo","definition":"Low phospholipid associated cholelithiasis is a rare genetic hepatic disease characterized by cholesterol gallstones and intrahepatic stones developing before the age of 40 years.","definition_xrefs":["Orphanet:69663"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholecystitis","termid":"MONDO:0002155"},{"relation_name":"is_a","term_name":"hereditary gallbladder disorder","termid":"MONDO:0700225"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03363":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"low phospholipid associated cholelithiasis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MedDRA:10068936","UMLS:C2609268","icd11.foundation:1261516421","OMIM:600803","MEDGEN:760527","SCTID:715577009","GARD:16683"],"synonyms":[{"name":"ABCB4 gene mutation-associated cholelithiasis","type":"exact"},{"name":"GBD1","type":"related"},{"name":"LPAC","type":"exact"},{"name":"cholelithiasis with ABCB4 gene mutation","type":"exact"},{"name":"cholelithiasis, Low phospholipid-associated","type":"related"},{"name":"gallbladder disease 1","type":"related"},{"name":"gallbladder disease type 1","type":"exact"}],"termid":"MONDO:0010939","terms_by_termid":{"MONDO:0010939":null},"xrefs":{"Monarch":{"xref_id":"0010939"}}}


id: PBO:0001453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate kinase Adk1","termid":"PBO:0001453"}


id: GO:1904938
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any Wnt signaling pathway, planar cell polarity pathway that is involved in axon guidance.","definition_xrefs":["GOC:bf","GO_REF:0000060","GOC:PARL","GOC:TermGenie","PMID:21106844","PMID:23517308"],"gene_count":0,"genotype_count":0,"name":"obsolete planar cell polarity pathway involved in axon guidance (obsolete GO:1904938)","synonyms":[{"name":"PCP pathway involved in axon chemotaxis","type":"related"},{"name":"PCP pathway involved in axon growth cone guidance","type":"narrow"},{"name":"PCP pathway involved in axon guidance","type":"exact"},{"name":"PCP pathway involved in axon pathfinding","type":"exact"},{"name":"Wnt receptor signaling pathway, planar cell polarity pathway involved in axon chemotaxis","type":"related"},{"name":"Wnt receptor signaling pathway, planar cell polarity pathway involved in axon growth cone guidance","type":"narrow"},{"name":"Wnt receptor signaling pathway, planar cell polarity pathway involved in axon guidance","type":"exact"},{"name":"Wnt receptor signaling pathway, planar cell polarity pathway involved in axon pathfinding","type":"exact"},{"name":"Wnt receptor signalling pathway, planar cell polarity pathway involved in axon chemotaxis","type":"related"},{"name":"Wnt receptor signalling pathway, planar cell polarity pathway involved in axon growth cone guidance","type":"narrow"},{"name":"Wnt receptor signalling pathway, planar cell polarity pathway involved in axon guidance","type":"exact"},{"name":"Wnt receptor signalling pathway, planar cell polarity pathway involved in axon pathfinding","type":"exact"},{"name":"Wnt signaling pathway, planar cell polarity pathway involved in axon chemotaxis","type":"related"},{"name":"Wnt signaling pathway, planar cell polarity pathway involved in axon growth cone guidance","type":"narrow"},{"name":"Wnt signaling pathway, planar cell polarity pathway involved in axon guidance","type":"exact"},{"name":"Wnt signaling pathway, planar cell polarity pathway involved in axon pathfinding","type":"exact"},{"name":"Wnt-JNK signaling pathway involved in axon chemotaxis","type":"related"},{"name":"Wnt-JNK signaling pathway involved in axon growth cone guidance","type":"related"},{"name":"Wnt-JNK signaling pathway involved in axon guidance","type":"related"},{"name":"Wnt-JNK signaling pathway involved in axon pathfinding","type":"related"},{"name":"Wnt-PCP signaling involved in axon guidance","type":"exact"},{"name":"Wnt-PCP signaling pathway involved in axon chemotaxis","type":"related"},{"name":"Wnt-PCP signaling pathway involved in axon growth cone guidance","type":"related"},{"name":"Wnt-PCP signaling pathway involved in axon guidance","type":"related"},{"name":"Wnt-PCP signaling pathway involved in axon pathfinding","type":"related"},{"name":"Wnt-activated signaling pathway, planar cell polarity pathway involved in axon chemotaxis","type":"related"},{"name":"Wnt-activated signaling pathway, planar cell polarity pathway involved in axon growth cone guidance","type":"narrow"},{"name":"Wnt-activated signaling pathway, planar cell polarity pathway involved in axon guidance","type":"exact"},{"name":"Wnt-activated signaling pathway, planar cell polarity pathway involved in axon pathfinding","type":"exact"},{"name":"non-canonical Wnt signaling pathway involved in axon chemotaxis","type":"related"},{"name":"non-canonical Wnt signaling pathway involved in axon growth cone guidance","type":"related"},{"name":"non-canonical Wnt signaling pathway involved in axon guidance","type":"related"},{"name":"non-canonical Wnt signaling pathway involved in axon pathfinding","type":"related"},{"name":"planar cell polarity pathway involved in axon chemotaxis","type":"related"},{"name":"planar cell polarity pathway involved in axon growth cone guidance","type":"narrow"},{"name":"planar cell polarity pathway involved in axon pathfinding","type":"exact"}],"termid":"GO:1904938"}


id: PBO:0061051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIPBL cohesin loading factor","termid":"PBO:0061051"}


id: PBO:0005461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic cohesin complex, non-SMC subunit Rad21 (kleisin)","termid":"PBO:0005461"}


id: MONDO:0022755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"monosomy","termid":"MONDO:0020639"},{"relation_name":"is_a","term_name":"chromosome 18 disorder","termid":"MONDO:0700125"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 18 mosaic monosomy","secondary_identifiers":["MEDGEN:419755","UMLS:C2931250","MESH:C536581"],"synonyms":[{"name":"Mosaic monosomy 18","type":"related"},{"name":"Mosaic monosomy chromosome 18","type":"related"},{"name":"monosomy 18 mosaicism","type":"related"}],"termid":"MONDO:0022755","xrefs":{"Monarch":{"xref_id":"0022755"}}}


id: GO:0007390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The spreading of the amnioserosa from its compressed state to cover the whole of the dorsal surface. Initiating in the thorax and spreading posteriorly, it is accompanied by the transition from a parasegmental to segmental division of the embryo.","definition_xrefs":["GOC:bf","PMID:12147138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"embryonic development via the syncytial blastoderm","termid":"GO:0001700"}],"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":"germ-band shortening","synonyms":[{"name":"germ-band retraction","type":"exact"}],"termid":"GO:0007390"}


id: PBO:0090699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIM23 translocase complex-associated motor subunit Pam17","termid":"PBO:0090699"}


id: MONDO:0017436
data:
  {"annotated_genes":["SJAG_03847","SJAG_01863"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009670"},{"annotations":[87218],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012656"}]},"cv_name":"mondo","definition":"A syndrome characterized by congenital nonprogressive joint contractures. The contractures can involve the upper or lower limbs and/or the vertebral column, leading to various degrees of flexion or extension limitations evident at birth.","definition_xrefs":["PMID:22610851","DOID:0060558"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"arthrogryposis syndrome","termid":"MONDO:0015225"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01863":null,"SJAG_03847":null},"genotype_count":0,"is_obsolete":false,"name":"lethal congenital contracture syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:253310","UMLS:C5848326","GARD:12643","MEDGEN:1863860","icd11.foundation:1866017256","Orphanet:294965"],"synonyms":[{"name":"LCCS","type":"exact"}],"termid":"MONDO:0017436","terms_by_termid":{"MONDO:0009670":null,"MONDO:0012656":null},"xrefs":{"Monarch":{"xref_id":"0017436"}}}


id: PBO:0055811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LPGAT1 antisense RNA 1","termid":"PBO:0055811"}


id: GO:0007564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of chitin-based cuticular tanning.","definition_xrefs":["GOC:go_curators","GOC:mtg_sensu","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal development","termid":"GO:2000026"},{"relation_name":"regulates","term_name":"chitin-based cuticle sclerotization","termid":"GO:0007593"}],"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 chitin-based cuticle tanning","synonyms":[{"name":"regulation of cuticle hardening","type":"narrow"},{"name":"regulation of cuticle tanning","type":"exact"}],"termid":"GO:0007564"}


id: GO:0044297
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of a cell bearing surface projections such as axons, dendrites, cilia, or flagella that includes the nucleus, but excludes all cell projections.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"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":"cell body","secondary_identifiers":["Wikipedia:Cell_body","FBbt:00005107","FMA:67301"],"synonyms":[{"name":"cell soma","type":"exact"}],"termid":"GO:0044297"}


id: MONDO:1012898
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteopetrosis that occurs in cattle due to a mutation in the SLC4A2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteopetrosis, cattle","termid":"MONDO:1011181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteopetrosis, SLC4A2-related, cattle","secondary_identifiers":["OMIA:002443-9913"],"termid":"MONDO:1012898","xrefs":{"Monarch":{"xref_id":"1012898"}}}


id: GO:0160062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the cutin-based cuticle over time, from its formation to the mature structure. Cutin-based cuticle is an extracellular structure composed of a covalently linked macromolecular scaffold of cutin and a variety of organic solvent-soluble lipids that are collectively termed waxes. Such structures are found on the external face of polysaccharide cell walls in land plants.","definition_xrefs":["PMID:23893170"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cutin-based cuticle development","termid":"GO:0160062"}


id: GO:0046464
data:
  {"annotated_genes":["SJAG_02089","SJAG_01036","SJAG_03604","SJAG_02543"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93670,119432,73170,100249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019433"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of acylglycerol, any mono-, di- or triester of glycerol with (one or more) fatty acids.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylglycerol metabolic process","termid":"GO:0006639"},{"relation_name":"is_a","term_name":"neutral lipid catabolic process","termid":"GO:0046461"},{"relation_name":"is_a","term_name":"glycerolipid catabolic process","termid":"GO:0046503"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01036":null,"SJAG_02089":null,"SJAG_02543":null,"SJAG_03604":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:0006629","GO:0008150"],"is_obsolete":false,"name":"acylglycerol catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"acylglycerol breakdown","type":"exact"},{"name":"acylglycerol catabolism","type":"exact"},{"name":"acylglycerol degradation","type":"exact"}],"termid":"GO:0046464","terms_by_termid":{"GO:0019433":null}}


id: FYPO:0002874
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the medial cortex begins earlier than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to medial cortex during vegetative growth","termid":"FYPO:0000731"},{"relation_name":"is_a","term_name":"premature protein localization to cell division site","termid":"FYPO:0007829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"premature protein localization to medial cortex during vegetative growth","synonyms":[{"name":"advanced protein localization to medial cortex during vegetative growth","type":"exact"},{"name":"faster protein localization to medial cortex during vegetative growth","type":"related"},{"name":"premature protein localisation to medial cortex during vegetative growth","type":"exact"},{"name":"premature protein localization to medial cortex during mitotic cell cycle","type":"related"},{"name":"premature protein localization to medial ring during vegetative growth","type":"exact"}],"termid":"FYPO:0002874"}


id: MONDO:0020628
data:
  {"annotated_genes":["SJAG_04816"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88158],"is_not":false,"summary":null,"term":"MONDO:0020628"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"microcephaly, growth restriction and increased sister chromatid exchange","termid":"MONDO:0020629"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04816":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"microcephaly, growth restriction, and increased sister chromatid exchange 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618097","GARD:18507","UMLS:C4748176","MEDGEN:1648384"],"synonyms":[{"name":"MGRISCE2","type":"related"},{"name":"microcephaly, growth restriction, and increased sister chromatid exchange 2","type":"exact"}],"termid":"MONDO:0020628","terms_by_termid":{"MONDO:0020628":null},"xrefs":{"Monarch":{"xref_id":"0020628"}}}


id: MOD:01854
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively adds one oxygen atom to a sulfur atom of a residue without removing hydrogen atoms.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur oxygenated residue","termid":"MOD:00680"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfur monooxygenated residue","termid":"MOD:01854"}


id: PBO:0057727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1302-11","termid":"PBO:0057727"}


id: MONDO:0800130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoinflammatory syndrome characterized by onset of various autoimmune features usually in the first decades of life, although later onset has been reported. Typical features include autoimmune cytopenia, hemolytic anemia, thrombocytopenia, and lymphadenopathy. More variable features may include autoimmune thyroiditis, psoriasis or eczema, nephritis, hepatitis, and symptoms of systemic lupus erythematosus (SL). Some patients may have recurrent infections or exacerbation of the disease with acute infection. Laboratory studies show variable findings, often decreased numbers of naive B cells, lymphopenia with skewed subsets, hypogammaglobulinemia, presence of autoantibodies, and a hyperinflammatory state. The disorder shows autosomal dominant inheritance with incomplete penetrance.","definition_xrefs":["OMIM:619375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoinflammatory syndrome with immunodeficiency","secondary_identifiers":["MEDGEN:1784363","UMLS:C5543547"],"termid":"MONDO:0800130","xrefs":{"Monarch":{"xref_id":"0800130"}}}


id: MONDO:0012695
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Meckel syndrome in which the cause of the disease is a mutation in the RPGRIP1L gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Meckel syndrome","termid":"MONDO:0018921"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meckel syndrome, type 5","secondary_identifiers":["GARD:15520","DOID:0070119","MESH:C566915","MEDGEN:409740","UMLS:C1969052","OMIM:611561"],"synonyms":[{"name":"MKS5","type":"exact"},{"name":"Meckel syndrome 5","type":"related"},{"name":"Meckel syndrome caused by mutation in RPGRIP1L","type":"exact"},{"name":"Meckel syndrome, type 5","type":"exact"},{"name":"Meckel-Gruber syndrome, type 5","type":"exact"},{"name":"RPGRIP1L Meckel syndrome","type":"exact"}],"termid":"MONDO:0012695","xrefs":{"Monarch":{"xref_id":"0012695"}}}


id: MONDO:0045020
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease that has its basis in the disruption of glycine metabolic process.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid metabolism disease","termid":"MONDO:0037871"},{"relation_name":"is_a","term_name":"disorder of organic acid metabolism","termid":"MONDO:0045022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"glycine metabolism disease","secondary_identifiers":["MEDGEN:541361","UMLS:C0268558","SCTID:83076007"],"synonyms":[{"name":"disorder of glycine metabolic process","type":"exact"},{"name":"disorder of glycine metabolism","type":"exact"},{"name":"glycine metabolic process disease","type":"exact"},{"name":"glycine metabolism disease","type":"exact"}],"termid":"MONDO:0045020","xrefs":{"Monarch":{"xref_id":"0045020"}}}


id: GO:1990034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of calcium ions from inside of a cell, across the plasma membrane and into the extracellular region.","definition_xrefs":["GOC:mah","PMID:2145281"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium ion transmembrane transport","termid":"GO:0070588"},{"relation_name":"is_a","term_name":"export across plasma membrane","termid":"GO:0140115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"calcium ion export across plasma membrane","synonyms":[{"name":"calcium ion efflux from cell","type":"exact"},{"name":"calcium ion export from cell","type":"exact"}],"termid":"GO:1990034"}


id: PBO:0087600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the BLOC-1 complex involved in endosomal maturation; interacts with Vps21p-GFP; has potential role in vacuolar function, as suggested by its ability to bind Vac8p; likely member of; Vab2p-GFP-fusion localizes to cytoplasm in punctate pattern","termid":"PBO:0087600"}


id: PBO:0004844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane alkaline phosphatase (predicted)","termid":"PBO:0004844"}


id: GO:0045819
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of glycogen.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glycogen catabolic process","termid":"GO:0005981"},{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"positive regulation of glycogen metabolic process","termid":"GO:0070875"},{"relation_name":"positively_regulates","term_name":"glycogen catabolic process","termid":"GO:0005980"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006091"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"positively_regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0006091","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"positive regulation of glycogen catabolic process","synonyms":[{"name":"activation of glycogen catabolic process","type":"narrow"},{"name":"positive regulation of glycogen breakdown","type":"exact"},{"name":"positive regulation of glycogen catabolism","type":"exact"},{"name":"positive regulation of glycogen degradation","type":"exact"},{"name":"positive regulation of glycogenolysis","type":"exact"},{"name":"stimulation of glycogen catabolic process","type":"narrow"},{"name":"up regulation of glycogen catabolic process","type":"exact"},{"name":"up-regulation of glycogen catabolic process","type":"exact"},{"name":"upregulation of glycogen catabolic process","type":"exact"}],"termid":"GO:0045819"}


id: MONDO:0002234
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-infectious or infectious inflammatory process affecting the vagina.","definition_xrefs":["NCIT:C26911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal disorder","termid":"MONDO:0001433"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vaginitis","secondary_identifiers":["UMLS:C0042267","SCTID:30800001","ICD9:616.1","icd11.foundation:290861382","MEDGEN:21815","DOID:2170","HP:0030683","MESH:D014627","ICD9:616.10"],"synonyms":[{"name":"inflammation of vagina","type":"exact"},{"name":"vagina inflammation","type":"exact"},{"name":"vaginal Inflammation","type":"exact"},{"name":"vaginal inflammation","type":"exact"},{"name":"vaginitis","type":"exact"},{"name":"vaginitis (disease)","type":"exact"}],"termid":"MONDO:0002234","xrefs":{"Monarch":{"xref_id":"0002234"}}}


id: GO:0016363
data:
  {"annotated_genes":["SJAG_02661","SJAG_03025"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[57443,81240],"is_not":false,"summary":null,"term":"GO:0016363"}]},"cv_name":"cellular_component","definition":"A dynamic, proteinaceous framework within the nucleus of eukaryotic cells, composed of proteins and RNA, that provides structural support for chromatin organization, gene regulation, and nuclear processes.","definition_xrefs":["PMID:15608168","PMID:3058729","PMID:39789220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"nuclear lumen","termid":"GO:0031981"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02661":null,"SJAG_03025":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0005575"],"is_obsolete":false,"name":"nuclear matrix","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000044":null},"secondary_identifiers":["Wikipedia:Nuclear_matrix"],"synonyms":[{"name":"nucleoskeleton","type":"exact"}],"termid":"GO:0016363","terms_by_termid":{"GO:0016363":null}}


id: GO:0060291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that modulates synaptic plasticity such that synapses are changed resulting in the increase in the rate, or frequency of synaptic transmission at the synapse.","definition_xrefs":["GOC:dph","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synaptic plasticity","termid":"GO:0048167"},{"relation_name":"is_a","term_name":"positive regulation of synaptic transmission","termid":"GO:0050806"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"long-term synaptic potentiation","synonyms":[{"name":"LTP","type":"related"},{"name":"long-term potentiation","type":"broad"}],"termid":"GO:0060291"}


id: GO:0004423
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of the 2-sulfate groups of the L-iduronate 2-sulfate units of dermatan sulfate, heparan sulfate and heparin.","definition_xrefs":["EC:3.1.6.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfuric ester hydrolase activity","termid":"GO:0008484"}],"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:0016788"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"iduronate-2-sulfatase activity","secondary_identifiers":["Reactome:R-HSA-1793182","MetaCyc:3.1.6.13-RXN","Reactome:R-HSA-9036046","Reactome:R-HSA-1678650","Reactome:R-HSA-2262743"],"synonyms":[{"name":"2-sulfo-L-iduronate 2-sulfatase activity","type":"related"},{"name":"L-iduronate 2-sulfate sulfatase activity","type":"related"},{"name":"L-iduronate-2-sulfate 2-sulfohydrolase activity","type":"related"},{"name":"L-idurono sulfate sulfatase activity","type":"related"},{"name":"L-iduronosulfatase activity","type":"related"},{"name":"chondroitinsulfatase","type":"broad"},{"name":"iduronate sulfatase activity","type":"related"},{"name":"iduronate sulfate sulfatase activity","type":"related"},{"name":"iduronate-2-sulfate sulfatase activity","type":"related"},{"name":"iduronate-2-sulphatase activity","type":"exact"},{"name":"iduronide-2-sulfate sulfatase activity","type":"related"},{"name":"idurono-2-sulfatase activity","type":"related"},{"name":"sulfo-L-iduronate sulfatase activity","type":"related"},{"name":"sulfoiduronate sulfohydrolase activity","type":"related"}],"termid":"GO:0004423"}


id: PBO:0027696
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_curved_cytoplasmic_microtubules","termid":"PBO:0027696"}


id: MONDO:0002467
data:
  {"annotated_genes":["SJAG_05313","SJAG_04755"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88939,88940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0968980"}]},"cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder affecting the inner ear. Causes are inner ear infections, head injuries, and neoplasms (e.g., acoustic schwannoma). Symptoms include dizziness, imbalance, nausea, and vision problems.","definition_xrefs":["NCIT:C27166"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auditory system disorder","termid":"MONDO:0002409"},{"relation_name":"is_a","term_name":"disorder of ear","termid":"MONDO:0021205"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04755":null,"SJAG_05313":null},"genotype_count":0,"is_obsolete":false,"name":"inner ear disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0009672","ICD10CM:H80-H83","UMLS:C0494559","SCTID:232297009","MESH:D007759","MEDGEN:141671","DOID:2952"],"synonyms":[{"name":"disease of internal ear","type":"exact"},{"name":"disease or disorder of internal ear","type":"exact"},{"name":"disorder of internal ear","type":"exact"},{"name":"inner Ear disorder","type":"exact"},{"name":"internal Ear disorder","type":"exact"},{"name":"internal ear disease","type":"exact"},{"name":"internal ear disease or disorder","type":"exact"},{"name":"labyrinthine disease","type":"exact"},{"name":"vestibular disorder","type":"narrow"}],"termid":"MONDO:0002467","terms_by_termid":{"MONDO:0968980":null},"xrefs":{"Monarch":{"xref_id":"0002467"}}}


id: MONDO:1011028
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ataxia telangiectasia that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ataxia telangiectasia, non-human animal","termid":"MONDO:1010249"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxia telangiectasia, pig","secondary_identifiers":["OMIA:002044-9823"],"termid":"MONDO:1011028","xrefs":{"Monarch":{"xref_id":"1011028"}}}


id: MONDO:0859346
data:
  {"annotated_genes":["SJAG_04884"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87346],"is_not":false,"summary":null,"term":"MONDO:0859346"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mosaic variegated aneuploidy syndrome","termid":"MONDO:0000141"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04884":null},"genotype_count":0,"is_obsolete":false,"name":"mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060982","UMLS:C5774284","MEDGEN:1824057","OMIM:620189"],"termid":"MONDO:0859346","terms_by_termid":{"MONDO:0859346":null},"xrefs":{"Monarch":{"xref_id":"0859346"}}}


id: MONDO:0023142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fetal brain disruption sequence","termid":"MONDO:0023142","xrefs":{"Monarch":{"xref_id":"0023142"}}}


id: GO:0018196
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-asparagine.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-asparagine modification (obsolete GO:0018196)","termid":"GO:0018196"}


id: PBO:0087139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein that binds specific mRNAs and interacts with She3p; part of the mRNA localization machinery that restricts accumulation of certain proteins to the bud; binds to ER-derived membranes and targets mRNAs to cortical ER","termid":"PBO:0087139"}


id: PBO:0058091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4307 host gene","termid":"PBO:0058091"}


id: GO:0019782
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the activation of the small ubiquitin-related modifier ISG15, through the formation of an ATP-dependent high-energy thiolester bond.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like modifier activating enzyme activity","termid":"GO:0008641"}],"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:0016874"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016874","GO:0140096"],"is_obsolete":false,"name":"ISG15 activating enzyme activity","synonyms":[{"name":"UBE1L","type":"narrow"}],"termid":"GO:0019782"}


id: FYPO:0002311
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of GMP binding by a gene product (usually a protein) in a mutant is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal GMP binding","termid":"FYPO:0002310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"decreased GMP binding","synonyms":[{"name":"reduced GMP binding","type":"exact"}],"termid":"FYPO:0002311"}


id: MONDO:0012122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Moyamoya disease","termid":"MONDO:0016820"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"moyamoya disease 3","secondary_identifiers":["MEDGEN:373326","OMIM:608796","UMLS:C1837418","GARD:15442","MESH:C536993"],"synonyms":[{"name":"MYMY3","type":"exact"},{"name":"Moyamoya disease 3","type":"related"}],"termid":"MONDO:0012122","xrefs":{"Monarch":{"xref_id":"0012122"}}}


id: MONDO:0006059
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that arises from the nasal cavity mucosa. Signs and symptoms include nasal fullness and obstruction, pain, epistaxis, and the presence of a nasal mass.","definition_xrefs":["NCIT:C8192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nasal cavity carcinoma","termid":"MONDO:0003212"},{"relation_name":"is_a","term_name":"head and neck squamous cell carcinoma","termid":"MONDO:0010150"}],"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":"nasal cavity squamous cell carcinoma","secondary_identifiers":["UMLS:C0280333","DOID:5515","EFO:1000057","MEDGEN:79104"],"synonyms":[{"name":"nasal cavity squamous cell carcinoma","type":"exact"},{"name":"squamous cell carcinoma of nasal cavity","type":"exact"},{"name":"squamous cell carcinoma of the nasal cavity","type":"exact"}],"termid":"MONDO:0006059","xrefs":{"Monarch":{"xref_id":"0006059"}}}


id: PBO:0083608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame unlikely to encode a functional protein; overlaps essential RRN5 gene which encodes a member of the UAF transcription factor involved in transcription of rDNA by RNA polymerase I","termid":"PBO:0083608"}


id: PBO:0053763
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 1005","termid":"PBO:0053763"}


id: MONDO:0018352
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma arising from the penis. It occurs chiefly in the squamous epithelium of the glans, coronal sulcus, and foreskin. Etiologic factors include phimosis, lichen sclerosus, smoking, ultraviolet irradiation, history of warts or condylomas, and lack of circumcision. Human papilloma virus is present in a subset of penile squamous cell carcinomas. Patients may present with an exophytic or flat ulcerative mass in the glans or a large primary tumor with inguinal nodal and skin metastases. Morphologic variants include the basaloid carcinoma, warty (condylomatous) carcinoma, verrucous carcinoma, and sarcomatoid (spindle cell) carcinoma. (WHO, 2004)","definition_xrefs":["NCIT:C7729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"penile carcinoma","termid":"MONDO:0006360"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"squamous cell carcinoma of penis","secondary_identifiers":["Orphanet:398058","DOID:5518","MEDGEN:116057","icd11.foundation:186592209","UMLS:C0238348","GARD:21639","ONCOTREE:PSCC","SCTID:403468003"],"synonyms":[{"name":"PSCC","type":"related"},{"name":"epidermoid carcinoma of penis","type":"exact"},{"name":"epidermoid carcinoma of the penis","type":"exact"},{"name":"epidermoid cell carcinoma of penis","type":"exact"},{"name":"epidermoid cell carcinoma of the penis","type":"exact"},{"name":"penile epidermoid carcinoma","type":"exact"},{"name":"penile epidermoid cell carcinoma","type":"exact"},{"name":"penile squamous car.(epidermoid)","type":"exact"},{"name":"penile squamous carcinoma (epidermoid)","type":"exact"},{"name":"penile squamous cell cancer","type":"exact"},{"name":"penile squamous cell carcinoma","type":"exact"},{"name":"penis squamous cell carcinoma","type":"exact"},{"name":"squamous cell carcinoma of penis","type":"exact"},{"name":"squamous cell carcinoma of the penis","type":"exact"}],"termid":"MONDO:0018352","xrefs":{"Monarch":{"xref_id":"0018352"}}}


id: RO:0002332
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"p regulates levels of c if p regulates some amount (PATO:0000070) of c","direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_related_to","termid":"RO:0002328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulates_levels_of","termid":"RO:0002332"}


id: GO:0048377
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into a lateral mesoderm cell in an environment that is neutral with respect to the developmental pathway; upon specification, the cell fate can be reversed.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesodermal cell fate specification","termid":"GO:0007501"},{"relation_name":"part_of","term_name":"lateral mesodermal cell fate commitment","termid":"GO:0048372"}],"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":"lateral mesodermal cell fate specification","synonyms":[{"name":"lateral mesoderm cell fate specification","type":"exact"},{"name":"lateral plate mesoderm cell fate specification","type":"exact"},{"name":"lateral plate mesodermal cell fate specification","type":"exact"}],"termid":"GO:0048377"}


id: PBO:0088171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xanthine-guanine phosphoribosyl transferase; required for xanthine utilization and for optimal utilization of guanine","termid":"PBO:0088171"}


id: PBO:0069557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 829, pseudogene","termid":"PBO:0069557"}


id: MONDO:0000534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mucoepidermoid carcinoma that involves the trachea.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucoepidermoid carcinoma","termid":"MONDO:0003036"},{"relation_name":"is_a","term_name":"trachea carcinoma","termid":"MONDO:0003184"}],"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":"trachea mucoepidermoid carcinoma","secondary_identifiers":["DOID:0050919","MEDGEN:835970","SCTID:707379000","UMLS:C3873401"],"synonyms":[{"name":"trachea mucoepidermoid carcinoma","type":"exact"}],"termid":"MONDO:0000534","xrefs":{"Monarch":{"xref_id":"0000534"}}}


id: PBO:0043373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clustered mitochondria homolog pseudogene 3","termid":"PBO:0043373"}


id: PBO:0053571
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 589","termid":"PBO:0053571"}


id: GO:0047257
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,2-diacyl-3-O-(alpha-D-glucopyranosyl)-sn-glycerol + UDP-D-glucose = UDP + 1,2-diacyl-3-O-(alpha-D-glucopyranosyl(1,2)-O-alpha-D-glucopyranosyl)-sn-glycerol.","definition_xrefs":["MetaCyc:2.4.1.208-RXN","EC:2.4.1.208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glycosyltransferase activity","termid":"GO:0008194"},{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"diglucosyl diacylglycerol synthase activity","secondary_identifiers":["RHEA:19165"],"synonyms":[{"name":"DGlcDAG synthase activity","type":"related"},{"name":"MGlcDAG (1->2) glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:1,2-diacyl-3-O-(alpha-D-glucopyranosyl)-sn-glycerol (1->2) glucosyltransferase activity","type":"related"},{"name":"diglucosyl diacylglycerol (DGlcDAG) synthase activity","type":"exact"},{"name":"monoglucosyl diacylglycerol (1->2) glucosyltransferase activity","type":"related"}],"termid":"GO:0047257"}


id: FYPO:0004478
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a protein that is not normally found in the mitochondrion is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein mislocalized to cytoplasm during vegetative growth","termid":"FYPO:0000783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"protein mislocalized to mitochondrion","synonyms":[{"name":"ectopic protein localization to mitochondrion","type":"exact"},{"name":"protein mislocalised to mitochondrion","type":"exact"},{"name":"protein mislocalised to mitochondrion during vegetative growth","type":"exact"},{"name":"protein mislocalized to mitochondrion during mitotic cell cycle","type":"related"},{"name":"protein mislocalized to mitochondrion during vegetative growth","type":"exact"}],"termid":"FYPO:0004478"}


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


id: PBO:0051364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 3-25 (pseudogene)","termid":"PBO:0051364"}


id: MONDO:0975958
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 97","secondary_identifiers":["OMIM:621057"],"termid":"MONDO:0975958","xrefs":{"Monarch":{"xref_id":"0975958"}}}


id: PBO:0052028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"JPT1 pseudogene 1","termid":"PBO:0052028"}


id: GO:0015195
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of L-threonine from one side of a membrane to the other. L-threonine is (2R*,3S*)-2-amino-3-hydroxybutanoic acid.","definition_xrefs":["GOC:mtg_transport","GOC:ai","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"},{"relation_name":"is_a","term_name":"L-amino acid transmembrane transporter activity","termid":"GO:0015179"}],"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":"L-threonine transmembrane transporter activity","secondary_identifiers":["GO:0015512"],"synonyms":[{"name":"L-threonine permease activity","type":"related"},{"name":"L-threonine transporter activity","type":"broad"},{"name":"threonine/serine:sodium symporter activity","type":"related"}],"termid":"GO:0015195"}


id: FYPO:0004352
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 nucleus is decreased during a cellular response to methylglyoxal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to nucleus during vegetative growth","termid":"FYPO:0001514"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein localization to nucleus during cellular response to methylglyoxal","synonyms":[{"name":"decreased protein localisation to nucleus during cellular response to methylglyoxal","type":"exact"},{"name":"decreased protein localization to nucleus during cellular response to methylglyoxal during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to nucleus during cellular response to methylglyoxal during vegetative growth","type":"exact"},{"name":"reduced protein localization to nucleus during cellular response to methylglyoxal","type":"exact"}],"termid":"FYPO:0004352"}


id: MONDO:0024880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant tumor that has spread from its original (primary) site of growth to another site close to or distant from the primary site.","definition_xrefs":["NCIT:C36263"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary malignant neoplasm","termid":"MONDO:0024881"},{"relation_name":"is_a","term_name":"metastatic neoplasm","termid":"MONDO:0024883"}],"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":"metastatic malignant neoplasm","secondary_identifiers":["MEDGEN:422475","UMLS:C2939419"],"synonyms":[{"name":"malignant metastatic neoplasm","type":"exact"},{"name":"metastatic cancer","type":"exact"},{"name":"metastatic malignant neoplasm","type":"exact"},{"name":"metastatic neoplasm, malignant","type":"exact"}],"termid":"MONDO:0024880","xrefs":{"Monarch":{"xref_id":"0024880"}}}


id: PBO:0056861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIB E3 ubiquitin protein ligase 1","termid":"PBO:0056861"}


id: PR:O13967
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- bgs2 gene.","definition_xrefs":["UniProtKB:O13967","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1,3-beta-glucan synthase component bgs2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24C9.07c","synonyms":[{"name":"1,3-beta-D-glucan-UDP glucosyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-bgs2","type":"exact"},{"name":"meiotic expression up-regulated protein 21 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13967"}


id: PBO:0050564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HRG pseudogene 2","termid":"PBO:0050564"}


id: FYPO:0004516
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 number of sites at which the protein Rad52 (also called Rad22) accumulates is lower than normal.","definition_xrefs":["PomBase:mah","PMID:22064477"],"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:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased number of Rad52 foci during vegetative growth","synonyms":[{"name":"decreased number of Rad22 foci during vegetative growth","type":"exact"},{"name":"decreased number of Rad52 foci during mitotic cell cycle","type":"related"},{"name":"reduced number of Rad52 foci during vegetative growth","type":"exact"}],"termid":"FYPO:0004516"}


id: PBO:0081665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 587","termid":"PBO:0081665"}


id: PBO:0062046
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 T member 33","termid":"PBO:0062046"}


id: PBO:0051394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda joining 2","termid":"PBO:0051394"}


id: MONDO:1012835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any muscular dystrophy that occurs in dogs due to a mutation in the COL6A3 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy, dog","termid":"MONDO:1010911"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscular dystrophy, COL6A3-related, dog","secondary_identifiers":["OMIA:002274-9615"],"synonyms":[{"name":"muscular dystrophy, Ullrich type, COL6A3-related, dog","type":"related"}],"termid":"MONDO:1012835","xrefs":{"Monarch":{"xref_id":"1012835"}}}


id: PBO:0038374
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-related_via_exposure_to","termid":"PBO:0038374"}


id: MONDO:0002596
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete chordoma (obsolete MONDO:0002596)","termid":"MONDO:0002596","xrefs":{"Monarch":{"xref_id":"0002596"}}}


id: PBO:0059985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 5","termid":"PBO:0059985"}


id: GO:0072292
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of epithelial cells within a renal tubule that contributes to metanephric proximal tubule morphogenesis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell migration involved in proximal tubule morphogenesis","termid":"GO:0072159"},{"relation_name":"is_a","term_name":"epithelial cell migration involved in metanephric nephron tubule morphogenesis","termid":"GO:0072290"},{"relation_name":"part_of","term_name":"metanephric proximal tubule morphogenesis","termid":"GO:0072288"}],"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":"epithelial cell migration involved in metanephric proximal tubule morphogenesis","termid":"GO:0072292"}


id: GO:0035334
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The proteolytic cleavages to the Notch protein that occur prior to ligand binding. A primary cleavage event within the extracellular domain whilst the Notch protein in still in the secretory pathway, leads to the transportation of a processed heterodimer to the cell surface.","definition_xrefs":["GOC:bf","PMID:12651094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein processing","termid":"GO:0016485"},{"relation_name":"part_of","term_name":"Notch receptor processing","termid":"GO:0007220"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051604","GO:0010467"],"is_obsolete":false,"name":"Notch receptor processing, ligand-independent","synonyms":[{"name":"Notch S1 cleavage","type":"narrow"}],"termid":"GO:0035334"}


id: PBO:0046515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endoplasmic reticulum lectin 1","termid":"PBO:0046515"}


id: PBO:0059275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L35 pseudogene 4","termid":"PBO:0059275"}


id: PBO:0028111
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_bis(5'-adenosyl)-hexaphosphatase_activity","termid":"PBO:0028111"}


id: GO:0000992
data:
  {"annotated_genes":["SJAG_03120","SJAG_03354","SJAG_05339","SJAG_00421"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89954],"is_not":false,"summary":null,"term":"GO:0000992"},{"annotations":[71484],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001002"},{"annotations":[71485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001003"},{"annotations":[79255,97366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001006"}]},"cv_name":"molecular_function","definition":"Binding to a specific upstream regulatory DNA sequence (transcription factor recognition sequence or binding site) located in cis relative to the transcription start site (i.e., on the same strand of DNA) of a gene transcribed by RNA polymerase III. The transcribed region might be contain a single gene or a cistron containing multiple genes.","definition_xrefs":["GOC:txnOH","PMID:12381659"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cis-regulatory region sequence-specific DNA binding","termid":"GO:0000987"},{"relation_name":"is_a","term_name":"RNA polymerase III transcription regulatory region sequence-specific DNA binding","termid":"GO:0001016"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00421":null,"SJAG_03120":null,"SJAG_03354":null,"SJAG_05339":null},"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:0003677"},{"rel_name":"is_a","termid":"GO:0000976"}],"interesting_parent_ids":["GO:0005488","GO:0000976","GO:0003674","GO:0003677"],"is_obsolete":false,"name":"RNA polymerase III cis-regulatory region sequence-specific DNA binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0000992","terms_by_termid":{"GO:0000992":null,"GO:0001002":null,"GO:0001003":null,"GO:0001006":null}}


id: PR:Q9C0Y4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- agl1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C0Y4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-glucosidase Agl1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB24D3.10c","synonyms":[{"name":"SPAPB24D3.10c","type":"related"},{"name":"Spom972h-agl1","type":"exact"},{"name":"agl","type":"related"},{"name":"maltase (Schizosaccharomyces pombe 972h-)","type":"broad"}],"termid":"PR:Q9C0Y4"}


id: GO:0007484
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the genitalia over time, from formation as part of the genital disc to the mature structure. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:ai","GOC:sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genitalia development","termid":"GO:0048806"},{"relation_name":"part_of","term_name":"genital disc development","termid":"GO:0035215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"imaginal disc-derived genitalia development","synonyms":[{"name":"genital development","type":"broad"}],"termid":"GO:0007484"}


id: GO:1904565
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a 1-oleoyl-sn-glycerol 3-phosphate stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:12139919"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"relation_name":"is_a","term_name":"response to organophosphorus","termid":"GO:0046683"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to 1-oleoyl-sn-glycerol 3-phosphate","synonyms":[{"name":"response to 1-oleoyl lysophosphatidic acid","type":"exact"},{"name":"response to LPA","type":"exact"},{"name":"response to lysophosphatidic acid","type":"exact"},{"name":"response to oleoyl lysophosphatidic acid","type":"exact"},{"name":"response to oleoyl-L-alpha-lysophosphatidic acid","type":"exact"}],"termid":"GO:1904565"}


id: MOD:01279
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other -","definition_xrefs":["Unimod:253#H","PubMed:11283024","PubMed:1443554"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crotonaldehyde","termid":"MOD:00576"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crotonaldehyde - site H","synonyms":[{"name":"Crotonaldehyde","type":"related"}],"termid":"MOD:01279"}


id: PBO:0005515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongator complex subunit Elp4 (predicted)","termid":"PBO:0005515"}


id: PBO:0052215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel modifier subfamily S member 2","termid":"PBO:0052215"}


id: GO:0046074
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of dTMP, deoxyribosylthymine monophosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside monophosphate catabolic process","termid":"GO:0009178"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleotide catabolic process","termid":"GO:0009223"},{"relation_name":"is_a","term_name":"dTMP metabolic process","termid":"GO:0046073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"dTMP catabolic process","synonyms":[{"name":"dTMP breakdown","type":"exact"},{"name":"dTMP catabolism","type":"exact"},{"name":"dTMP degradation","type":"exact"}],"termid":"GO:0046074"}


id: PBO:0079087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Tyr (anticodon GTA) 4-1","termid":"PBO:0079087"}


id: MONDO:0018330
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mucinous adenocarcinoma of the appendix is a very rare, slow growing, well-differentiated epithelial neoplasm of the appendix characterized by abundant mucin production. Clinically, it presents as acute appendicitis (with abdominal pain, fever, leukocytosis) or as pseudomyxoma peritonei (wide-spread presence of mucin within the peritoneal cavity), however some patients may be completely asymptomatic at the time of diagnosis. In many cases, a second gastrointestinal malignancy is present.","definition_xrefs":["Orphanet:391723"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon mucinous adenocarcinoma","termid":"MONDO:0005007"},{"relation_name":"is_a","term_name":"appendix adenocarcinoma","termid":"MONDO:0006087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"mucinous adenocarcinoma of the appendix","secondary_identifiers":["MEDGEN:317382","ONCOTREE:MAAP","GARD:21629","icd11.foundation:425095558","NCIT:C43558","UMLS:C1706832"],"synonyms":[{"name":"appendiceal mucinous adenocarcinoma","type":"exact"},{"name":"appendix mucinous adenocarcinoma","type":"exact"},{"name":"vermiform appendix mucinous adenocarcinoma","type":"exact"}],"termid":"MONDO:0018330","xrefs":{"Monarch":{"xref_id":"0018330"}}}


id: PR:O14295
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- plr1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14295"],"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":"pyridoxal reductase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9E9.11","synonyms":[{"name":"PL reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PL-red (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-plr1","type":"exact"}],"termid":"PR:O14295"}


id: FYPO:0007205
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 replication fork arrest at sites within the eukaryotic rDNA repeat spacer is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype during vegetative growth","termid":"FYPO:0001334"},{"relation_name":"is_a","term_name":"DNA metabolism phenotype during vegetative growth","termid":"FYPO:0001346"},{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal replication fork arrest","termid":"FYPO:0008191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000002","FYPO:0001312","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal replication fork arrest at rDNA repeats","synonyms":[{"name":"normal replication fork arrest at rDNA repeats during mitotic cell cycle","type":"related"},{"name":"normal replication fork arrest at rDNA repeats during vegetative growth","type":"exact"},{"name":"normal replication fork arrest at ribosomal DNA repeats","type":"exact"}],"termid":"FYPO:0007205"}


id: PBO:0060827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NECTIN2 pseudogene 1","termid":"PBO:0060827"}


id: FYPO:0003992
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to menadione is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during vegetative growth","termid":"FYPO:0001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal RNA level during cellular response to menadione","synonyms":[{"name":"normal RNA accumulation during cellular response to menadione","type":"related"},{"name":"normal RNA level during cellular response to menadione during mitotic cell cycle","type":"related"},{"name":"normal RNA level during cellular response to menadione during vegetative growth","type":"exact"},{"name":"normal mRNA level during cellular response to menadione","type":"narrow"},{"name":"normal transcript level during cellular response to menadione","type":"exact"}],"termid":"FYPO:0003992"}


id: MONDO:1060107
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any disorder of oxysterol accumulation caused by biallelic loss of function variants in the CYP7B1 gene. A disorder of oxysterol accumulation is a condition where there is an abnormal buildup of oxysterols, which are oxidized cholesterol derivatives, in the body.","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"CYP7B1-related disorder of oxysterol accumulation","synonyms":[{"name":"CYP7B1-related disorder of oxysterol accumulation","type":"exact"}],"termid":"MONDO:1060107","xrefs":{"Monarch":{"xref_id":"1060107"}}}


id: PBO:0040897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 ribosome biogenesis factor","termid":"PBO:0040897"}


id: GO:1902295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any DNA replication, synthesis of RNA primer that is involved in cell cycle DNA replication.","definition_xrefs":["GOC:TermGenie","GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete synthesis of RNA primer involved in cell cycle DNA replication (obsolete GO:1902295)","synonyms":[{"name":"DNA replication, synthesis of RNA primer involved in cell cycle DNA replication","type":"exact"},{"name":"replication priming involved in cell cycle DNA replication","type":"related"}],"termid":"GO:1902295"}


id: PBO:0071551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 16","termid":"PBO:0071551"}


id: PBO:0040025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"armadillo repeat containing X-linked 1","termid":"PBO:0040025"}


id: SO:0000822
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome originating in a cyanelle.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"cyanelle_sequence","termid":"SO:0000746"},{"relation_name":"is_a","term_name":"chromosome","termid":"SO:0000340"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyanelle_chromosome","synonyms":[{"name":"cyanelle chromosome","type":"exact"}],"termid":"SO:0000822"}


id: PR:000085729
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.1, 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":["PMID:19362535","PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3.1, initiator methionine removed form (Schizosaccharomyces pombe)","termid":"PR:000027574"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hht1/Me:(K9),UnPhos(S10)","pombase_gene_id":"SPAC1834.04","synonyms":[{"name":"PRO_0000221366, Lys-10, MOD:00663|Ser-11, PR:000026291","type":"related"},{"name":"PomBase_original_PRO_term_name: histone H3.1, initiator methionine removed K9-methylated and unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hht1/InitMet-/K9MeUnPhos:1","type":"exact"},{"name":"UniProtKB:P09988, 2-136, Lys-10, MOD:00663|Ser-11, PR:000026291","type":"related"},{"name":"hht1/Me:(K9),UnPhos(S10)","type":"exact"}],"termid":"PR:000085729"}


id: PBO:0041097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain and WD repeat domain containing 1 pseudogene 2","termid":"PBO:0041097"}


id: PBO:0053695
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 895","termid":"PBO:0053695"}


id: PATO:0001297
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A radiation reflective quality inhering in a bearer by virtue of the ratio of the energy of a wave reflected from its surface to the energy possessed by the wave striking the bearer's surface.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"radiation reflective quality","termid":"PATO:0001294"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reflectivity","termid":"PATO:0001297"}


id: PBO:0059101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mortality factor 4 like 1 pseudogene 7","termid":"PBO:0059101"}


id: PBO:0090329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichyl-phosphate-glucose-glycolipid alpha-glucosyltransferase Alg10, low frequency splice site, possible frameshifted","termid":"PBO:0090329"}


id: GO:0000767
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The change in form (cell shape and size) that occurs during sexual reproduction in order to facilitate direct contact between the compatible mating types.","definition_xrefs":["GOC:elh"],"gene_count":0,"genotype_count":0,"name":"obsolete cell morphogenesis involved in conjugation (obsolete GO:0000767)","termid":"GO:0000767"}


id: GO:0032875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of DNA endoreduplication.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of DNA-templated DNA replication","termid":"GO:0090329"},{"relation_name":"regulates","term_name":"DNA endoreduplication","termid":"GO:0042023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0006260","GO:0007049"],"is_obsolete":false,"name":"regulation of DNA endoreduplication","synonyms":[{"name":"regulation of DNA endoreplication","type":"exact"},{"name":"regulation of DNA re-duplication","type":"exact"}],"termid":"GO:0032875"}


id: PBO:0072761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S100 calcium binding protein A12","termid":"PBO:0072761"}


id: PBO:0057969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3689b","termid":"PBO:0057969"}


id: GO:1990103
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein-DNA complex containing DNA-bound DnaA attached to HU. HU is a dimer encoded by two closely related genes. Essential for the initiation of replication in bacteria; stimulates the DnaA-dependent unwinding of oriC.","definition_xrefs":["GOC:bhm","PMID:18179598"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primosome complex","termid":"GO:1990077"}],"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:0032991"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005694","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"DnaA-HU complex","synonyms":[{"name":"DnaA-HU-DNA complex","type":"exact"}],"termid":"GO:1990103"}


id: PBO:0040922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast cancer associated ESR1 regulating natural antisense transcript 1","termid":"PBO:0040922"}


id: FYPO:0007983
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed during mitotic interphase in which some microtubule bundles are not anchored to the nuclear membrane. See PMID:15068790","definition_xrefs":["PomBase:mlr","PMID:15068790"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule bundle","termid":"FYPO:0005558"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0002399","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"microtubule bundles detached from the nuclear envelope","termid":"FYPO:0007983"}


id: PBO:0048782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit alpha 13","termid":"PBO:0048782"}


id: GO:2000548
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of dendritic cell dendrite assembly.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of plasma membrane bounded cell projection assembly","termid":"GO:0120033"},{"relation_name":"is_a","term_name":"regulation of dendritic cell dendrite assembly","termid":"GO:2000547"},{"relation_name":"negatively_regulates","term_name":"dendritic cell dendrite assembly","termid":"GO:0097026"}],"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 dendritic cell dendrite assembly","synonyms":[{"name":"negative regulation of dendritic extension","type":"related"}],"termid":"GO:2000548"}


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


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


id: SO:0000761
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000761 phagemid_clone (obsolete SO:0000761)","termid":"SO:0000761"}


id: GO:0140775
data:
  {"annotated_genes":["SJAG_03025"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94315],"is_not":false,"summary":null,"term":"GO:0140775"}]},"cv_name":"molecular_function","definition":"Binding to an actin filament and promoting the dissociation of an actin filament branch.","definition_xrefs":["PMID:20362448"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex destabilizing activity","termid":"GO:0140776"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03025":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"actin filament debranching activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"actin debranching activity","type":"exact"}],"termid":"GO:0140775","terms_by_termid":{"GO:0140775":null}}


id: MONDO:0012412
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any classic complement early component deficiency in which the cause of the disease is a mutation in the C7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"classic complement early component deficiency","termid":"MONDO:0000015"},{"relation_name":"is_a","term_name":"immunodeficiency due to a late component of complement deficiency","termid":"MONDO:0015700"}],"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":"complement component 7 deficiency","secondary_identifiers":["OMIM:610102","MEDGEN:355270","NANDO:2200785","DOID:0060300","UMLS:C1864694","GARD:18290","MESH:C566443"],"synonyms":[{"name":"C7 classic complement early component deficiency","type":"exact"},{"name":"C7 deficiency","type":"related"},{"name":"C7D","type":"related"},{"name":"classic complement early component deficiency caused by mutation in C7","type":"exact"},{"name":"complement component 7 deficiency","type":"exact"}],"termid":"MONDO:0012412","xrefs":{"Monarch":{"xref_id":"0012412"}}}


id: PBO:0086655
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; haploid deletion mutant exhibits synthetic phenotype with alpha-synuclein; SWAT-GFP fusion protein localizes to the endoplasmic reticulum while mCherry fusion protein localizes to both the endoplasmic reticulum and vacuole","termid":"PBO:0086655"}


id: GO:0019373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways by which arachidonic acid is converted to other compounds including epoxyeicosatrienoic acids and dihydroxyeicosatrienoic acids.","definition_xrefs":["PMID:17979511","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arachidonate metabolic process","termid":"GO:0019369"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"epoxygenase P450 pathway","secondary_identifiers":["Reactome:R-HSA-2142670"],"termid":"GO:0019373"}


id: GO:0070731
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of cyclic GMP (cGMP), into, out of or within a cell.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanine nucleotide transport","termid":"GO:0001408"},{"relation_name":"is_a","term_name":"organic anion transport","termid":"GO:0015711"},{"relation_name":"is_a","term_name":"purine ribonucleotide transport","termid":"GO:0015868"},{"relation_name":"is_a","term_name":"cyclic nucleotide transport","termid":"GO:0070729"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"cGMP transport","synonyms":[{"name":"cyclic GMP transport","type":"exact"}],"termid":"GO:0070731"}


id: GO:0140781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ilicicolin H, a 4-hydroxy-2-pyridone alkaloid that has potent and broad antifungal activities by inhibiting the mitochondrial respiration chain.","definition_xrefs":["PMID:30905148","PMID:34947016","PMID:31216742"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkaloid biosynthetic process","termid":"GO:0009821"},{"relation_name":"is_a","term_name":"polyketide biosynthetic process","termid":"GO:0030639"},{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"mycotoxin biosynthetic process","termid":"GO:0043386"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"pyridine-containing compound biosynthetic process","termid":"GO:0072525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"ilicicolin H biosynthetic process","synonyms":[{"name":"ilicicolin H anabolism","type":"exact"},{"name":"ilicicolin H biosynthesis","type":"exact"},{"name":"ilicicolin H formation","type":"exact"},{"name":"ilicicolin H synthesis","type":"exact"}],"termid":"GO:0140781"}


id: PBO:0031248
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_poly(A)+_mRNA_export_from_nucleus","termid":"PBO:0031248"}


id: GO:0075086
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism stops, prevents, or reduces the frequency, rate or extent of transmembrane receptor-mediated cAMP signal transduction in the symbiont. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by host of symbiont transmembrane receptor-mediated cAMP signal transduction (obsolete GO:0075086)","synonyms":[{"name":"downregulation by host of symbiont transmembrane receptor-mediated cAMP signal transduction","type":"exact"},{"name":"inhibition by host of symbiont transmembrane receptor-mediated cAMP signal transduction","type":"narrow"},{"name":"negative regulation by host of symbiont transmembrane receptor-mediated cAMP signaling","type":"exact"}],"termid":"GO:0075086"}


id: FYPO:0001181
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of maltose alpha-glucosidase (also known as maltase) activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal alpha-glucosidase activity","termid":"FYPO:0001182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000257","FYPO:0000652"],"is_obsolete":false,"name":"normal maltase activity","synonyms":[{"name":"normal maltose alpha-glucosidase activity","type":"exact"}],"termid":"FYPO:0001181"}


id: PBO:0116305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translation termination factor eRF3; has a role in mRNA deadenylation and decay; altered protein conformation creates the [PSI(+)] prion, self-perpetuating amyloid fibrils that modify cellular fitness, alter translational fidelity by affecting reading frame selection, and result in a nonsense suppressor phenotype; forms reversible liquid condensates in response to both acidic and osmotic stress to promote survival; many stress-response genes are repressed in the presence of [PSI(+)]","termid":"PBO:0116305"}


id: GO:1905752
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of argininosuccinate synthase activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:19491403"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of argininosuccinate synthase activity (obsolete GO:1905752)","synonyms":[{"name":"regulation of L-citrulline:L-aspartate ligase (AMP-forming)","type":"exact"},{"name":"regulation of arginine succinate synthetase activity","type":"exact"},{"name":"regulation of argininosuccinate synthetase activity","type":"exact"},{"name":"regulation of argininosuccinic acid synthetase activity","type":"exact"},{"name":"regulation of arginosuccinate synthetase activity","type":"exact"},{"name":"regulation of citrulline--aspartate ligase activity","type":"exact"}],"termid":"GO:1905752"}


id: PBO:0043685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COTL1 pseudogene 1","termid":"PBO:0043685"}


id: MONDO:0003223
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A solitary fibrous tumor/hemangiopericytoma that arises from the meninges.","definition_xrefs":["NCIT:C4660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangiopericytoma","termid":"MONDO:0005094"},{"relation_name":"is_a","term_name":"malignant tumor of meninges","termid":"MONDO:0021322"}],"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":"meninges hemangiopericytoma","secondary_identifiers":["DOID:4957","MEDGEN:83894","ONCOTREE:HPCCNS","UMLS:C0349622","SCTID:277522009"],"synonyms":[{"name":"hemangiopericytoma of meninges","type":"exact"},{"name":"hemangiopericytoma of the central nervous system","type":"related"},{"name":"hemangiopericytoma of the meninges","type":"exact"},{"name":"meningeal cluster hemangiopericytoma","type":"exact"},{"name":"meningeal cluster spindle cell tumor","type":"exact"},{"name":"meningeal cluster spindle cell tumour","type":"exact"},{"name":"meningeal hemangiopericytoma","type":"exact"},{"name":"meningeal solitary fibrous tumor/hemangiopericytoma","type":"exact"},{"name":"meninges hemangiopericytoma","type":"exact"}],"termid":"MONDO:0003223","xrefs":{"Monarch":{"xref_id":"0003223"}}}


id: MONDO:0011396
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse palmoplantar keratoderma, characterized by honeycomb palmoplantar hyperkeratosis associated with pseudoainhum of the fifth digit of the hand, ichthyosis and deafness. Keratoderma hereditarium mutilans with ichthyosis follows an autosomal dominant mode of transmission.","definition_xrefs":["Orphanet:79395"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse palmoplantar keratoderma","termid":"MONDO:0017666"}],"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":"loricrin keratoderma","secondary_identifiers":["MESH:C565826","GARD:16719","SCTID:717183001","UMLS:C1858805","MEDGEN:395099","OMIM:604117"],"synonyms":[{"name":"Camisa disease","type":"exact"},{"name":"Vohwinkel syndrome with ichthyosis","type":"exact"},{"name":"Vohwinkel syndrome, variant form","type":"related"},{"name":"keratoderma hereditarium mutilans with ichthyosis","type":"exact"},{"name":"keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome","type":"exact"},{"name":"loricrin keratoderma","type":"exact"},{"name":"mutilating keratoderma with ichthyosis","type":"related"}],"termid":"MONDO:0011396","xrefs":{"Monarch":{"xref_id":"0011396"}}}


id: MONDO:0000459
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A molecular subtype of glioblastoma characterized by the presence of NF1 mutations.","definition_xrefs":["NCIT:C111695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glioblastoma","termid":"MONDO:0018177"}],"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":"mesenchymal glioblastoma","secondary_identifiers":["DOID:0050805","UMLS:C3829122","MEDGEN:821870"],"synonyms":[{"name":"glioblastoma mesenchymal subtype","type":"related"},{"name":"mesenchymal glioblastoma","type":"exact"}],"termid":"MONDO:0000459","xrefs":{"Monarch":{"xref_id":"0000459"}}}


id: MOD:00169
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to N-cysteinyl-glycosylphosphatidylinositolethanolamine.","definition_xrefs":["PubMed:2897081","RESID:AA0160"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosylphosphatidylinositolated residue","termid":"MOD:00818"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"},{"rel_name":"is_a","termid":"MOD:01155"},{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764","MOD:01155","MOD:00905"],"is_obsolete":false,"name":"N-cysteinyl-glycosylphosphatidylinositolethanolamine","synonyms":[{"name":"GPICys","type":"exact"},{"name":"LIPID GPI-anchor amidated cysteine","type":"exact"},{"name":"N-cysteinyl-glycosylphosphatidylinositolethanolamine","type":"exact"}],"termid":"MOD:00169"}


id: GO:0097626
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of L-arginine from one side of a membrane to the other. In low-affinity transport the transporter is able to bind the solute only if it is present at very high concentrations.","definition_xrefs":["PMID:8195186","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-arginine transmembrane transporter activity","termid":"GO:0061459"},{"relation_name":"is_a","term_name":"low-affinity basic amino acid transmembrane transporter activity","termid":"GO:0097625"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"low-affinity L-arginine transmembrane transporter activity","synonyms":[{"name":"low affinity L-arginine transmembrane transporter activity","type":"exact"}],"termid":"GO:0097626"}


id: PBO:0086840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein with sequence similar to hydroxyacid dehydrogenases; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm","termid":"PBO:0086840"}


id: PATO:0002469
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Structural quality inhereing in a bearer in which a joint has apposed bony surfaces united by fibrous tissue, permitting no movement; found only between bones.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sutured to","termid":"PATO:0002469"}


id: FYPO:0000632
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype that affects mitochondrial translation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation phenotype","termid":"FYPO:0000291"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"mitochondrial translation phenotype","synonyms":[{"name":"fission yeast mitochondrial translation phenotype","type":"exact"},{"name":"mitochondrial translation phenotype during mitotic cell cycle","type":"related"},{"name":"mitochondrial translation phenotype during vegetative growth","type":"exact"}],"termid":"FYPO:0000632"}


id: SO:0001049
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An island that contains genes for integration/excision and the gene and site for the initiation of intercellular transfer by conjugation. It can be complemented for transfer by a conjugative transposon.","definition_xrefs":["Phigo:ariane"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genomic_island","termid":"SO:0000772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defective_conjugative_transposon","synonyms":[{"name":"defective conjugative transposon","type":"exact"}],"termid":"SO:0001049"}


id: PBO:0073369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SERTA domain containing 2","termid":"PBO:0073369"}


id: PBO:0076002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stromal interaction molecule 1","termid":"PBO:0076002"}


id: GO:1900947
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of isoprene biosynthetic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lipid biosynthetic process","termid":"GO:0046890"},{"relation_name":"is_a","term_name":"regulation of olefin biosynthetic process","termid":"GO:1900911"},{"relation_name":"is_a","term_name":"regulation of isoprene metabolic process","termid":"GO:1900944"},{"relation_name":"regulates","term_name":"isoprene biosynthetic process","termid":"GO:0043612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of isoprene biosynthetic process","synonyms":[{"name":"regulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"regulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"regulation of hemiterpene biosynthesis","type":"exact"},{"name":"regulation of hemiterpene biosynthetic process","type":"exact"}],"termid":"GO:1900947"}


id: MONDO:0100372
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any peroxisomal single enzyme/protein defect that disrupts peroxisomal transport.","definition_xrefs":["PMID:26611709","MONDO:patterns/specific_disease_by_disrupted_process","PMID:17055078"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisomal single enzyme/protein defect","termid":"MONDO:0100257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0019053","MONDO:0005066"],"is_obsolete":false,"name":"disorder of peroxisomal transporter","synonyms":[{"name":"disorder of peroxisomal transporter defect","type":"exact"}],"termid":"MONDO:0100372","xrefs":{"Monarch":{"xref_id":"0100372"}}}


id: GO:0070833
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The phosphatidylcholine biosynthetic process that begins with an initial N-methylation with phospho-base phosphoethanolamine, followed by two downstream N-methylations on phosphatidyl-bases, phosphatidyl-N-methylethanolamine and phosphatidyl-N-dimethylethanolamine. The process ends with the conversion of a phosphatidyl-N-dimethylethanolamine to a phosphatidylcholine.","definition_xrefs":["MetaCyc:PWY4FS-3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylcholine biosynthetic process","termid":"GO:0006656"},{"relation_name":"is_a","term_name":"primary amino compound metabolic process","termid":"GO:1901160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"phosphatidylcholine biosynthesis from phosphoryl-ethanolamine via CDP-N-methylethanolamine","termid":"GO:0070833"}


id: GO:1900427
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A regulation of transcription from RNA polymerase II promoter that results in regulation of cellular response to oxidative stress.","definition_xrefs":["GOC:mah","GOC:TermGenie","PMID:10348908"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular response to oxidative stress by regulation of transcription from RNA polymerase II promoter (obsolete GO:1900427)","synonyms":[{"name":"regulation of adaptive response to oxidative stress by regulation of transcription from RNA polymerase II promoter","type":"narrow"}],"termid":"GO:1900427"}


id: GO:0019898
data:
  {"annotated_genes":["SJAG_01043","SJAG_04026","SJAG_01911","SJAG_00852","SJAG_03563","SJAG_00655","SJAG_04860","SJAG_00933","SJAG_02699","SJAG_02233","SJAG_00576","SJAG_00114","SJAG_01876","SJAG_04000","SJAG_03403","SJAG_01249","SJAG_04552","SJAG_00230","SJAG_02605","SJAG_03081","SJAG_02444","SJAG_04642","SJAG_05398","SJAG_00721","SJAG_03456"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104749],"is_not":false,"summary":null,"term":"GO:0019898"},{"annotations":[112365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031234"},{"annotations":[105556,102242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099616"},{"annotations":[103069,61181,62742,108672,109980,108012,111331,64692,92646,66208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031314"},{"annotations":[109023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031315"},{"annotations":[96396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097629"},{"annotations":[96397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097632"},{"annotations":[76982,108306,82093,75892],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005834"},{"annotations":[73243,78974,96400,78459,113350],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034271"},{"annotations":[78975,107517,73244,78460],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034272"}]},"cv_name":"cellular_component","definition":"The component of a membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:mah","GOC:dos","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"membrane","termid":"GO:0016020"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_00230":null,"SJAG_00576":null,"SJAG_00655":null,"SJAG_00721":null,"SJAG_00852":null,"SJAG_00933":null,"SJAG_01043":null,"SJAG_01249":null,"SJAG_01876":null,"SJAG_01911":null,"SJAG_02233":null,"SJAG_02444":null,"SJAG_02605":null,"SJAG_02699":null,"SJAG_03081":null,"SJAG_03403":null,"SJAG_03456":null,"SJAG_03563":null,"SJAG_04000":null,"SJAG_04026":null,"SJAG_04552":null,"SJAG_04642":null,"SJAG_04860":null,"SJAG_05398":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"extrinsic component of membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0030396","Wikipedia:Peripheral_membrane_protein"],"synonyms":[{"name":"extrinsic to membrane","type":"exact"},{"name":"peripheral membrane protein","type":"exact"}],"termid":"GO:0019898","terms_by_termid":{"GO:0005834":null,"GO:0019898":null,"GO:0031234":null,"GO:0031314":null,"GO:0031315":null,"GO:0034271":null,"GO:0034272":null,"GO:0097629":null,"GO:0097632":null,"GO:0099616":null}}


id: PBO:0082235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-glucoside permease; transports maltose, maltotriose, alpha-methylglucoside, and turanose; almost identical to Mph3p; encoded in a subtelomeric position in a region likely to have undergone duplication","termid":"PBO:0082235"}


id: PBO:0038720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin gamma 1 pseudogene 15","termid":"PBO:0038720"}


id: PBO:0081848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 781","termid":"PBO:0081848"}


id: GO:0090570
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex, located in the nucleus, that possesses activity that prevents or downregulates transcription from a RNA polymerase I promoter.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription repressor complex","termid":"GO:0017053"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"RNA polymerase I transcription repressor complex","termid":"GO:0090570"}


id: GO:0052807
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: aflatoxin + 1,5-dihydrocoenzyme F420 = aflatoxin with reduced furanocoumarin moiety + coenzyme F420. 1,5-dihydrocoenzyme F420 is also known as reduced coenzyme F420.","definition_xrefs":["GOC:mengo_curators","PMID:20807200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors","termid":"GO:0016667"}],"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":"aflatoxin reductase (coenzyme F420) activity","synonyms":[{"name":"aflatoxin:coenzyme F420 oxidoreductase activity","type":"exact"},{"name":"aflatoxin:reduced coenzyme F420 reductase activity","type":"exact"},{"name":"coenzyme F420-aflatoxin reductase activity","type":"exact"},{"name":"coenzyme F420-dependent aflatoxin reductase activity","type":"exact"}],"termid":"GO:0052807"}


id: PBO:0091917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase, translational elongation factor eEF1","termid":"PBO:0091917"}


id: PBO:0001387
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"function depends on a functional spindle assembly checkpoint","termid":"PBO:0001387"}


