# terms

id: PR:O74363
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sqs1 gene.","definition_xrefs":["UniProtKB:O74363","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":"G-patch and R3H domain-containing protein C30B4.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC30B4.02c","synonyms":[{"name":"Spom972h-sqs1","type":"exact"}],"termid":"PR:O74363"}


id: PBO:0038441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha and gamma adaptin binding protein","termid":"PBO:0038441"}


id: PBO:0084079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-cyclohydrolase I, catalyzes first step in folic acid biosynthesis; human homolog GCH1 is implicated in dopa-responsive dystonia (DRD), and can complement yeast null mutant","termid":"PBO:0084079"}


id: GO:2000616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of histone H3-K9 acetylation.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of histone H3-K9 acetylation (obsolete GO:2000616)","synonyms":[{"name":"negative regulation of histone H3 acetylation at K9","type":"exact"},{"name":"negative regulation of histone H3K9 acetylation","type":"exact"}],"termid":"GO:2000616"}


id: PBO:0039273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG1 like 1, pseudogene","termid":"PBO:0039273"}


id: MONDO:1012000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sudden acquired retinal degeneration syndrome, non-human animal","secondary_identifiers":["OMIA:002169"],"synonyms":[{"name":"SARDS","type":"exact"}],"termid":"MONDO:1012000","xrefs":{"Monarch":{"xref_id":"1012000"}}}


id: GO:0004109
data:
  {"annotated_genes":["SJAG_04944"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[80248],"is_not":false,"summary":null,"term":"GO:0004109"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: coproporphyrinogen III + 2 H+ + O2 = 2 CO2 + 2 H2O + protoporphyrinogen IX.","definition_xrefs":["EC:1.3.3.3","RHEA:18257"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor","termid":"GO:0016634"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04944":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"coproporphyrinogen oxidase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R03220","MetaCyc:RXN0-1461","Reactome:R-HSA-189421"],"synonyms":[{"name":"coprogen oxidase activity","type":"exact"},{"name":"coproporphyrinogen-III oxidase activity","type":"exact"},{"name":"coproporphyrinogen:oxygen oxidoreductase (decarboxylating)","type":"related"},{"name":"coproporphyrinogenase activity","type":"exact"}],"termid":"GO:0004109","terms_by_termid":{"GO:0004109":null}}


id: PBO:0005585
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orthologous to S. cerevisiae YBR194W","termid":"PBO:0005585"}


id: PBO:0012283
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"switching of mating type","termid":"PBO:0012283"}


id: MONDO:0011264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary dystonia DYT6 type is characterized by focal, predominantly cranio-cervical dystonia with dysarthria and dysphagia, or limb dystonia in some cases.","definition_xrefs":["Orphanet:98806"],"direct_ancestors":[{"relation_name":"is_a","term_name":"generalized dystonia","termid":"MONDO:0000476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"torsion dystonia 6","secondary_identifiers":["SCTID:702448007","DOID:0090039","UMLS:C1414216","GARD:9630","NANDO:1200517","NCIT:C156361","OMIM:602629","MEDGEN:236274","MESH:C538003"],"synonyms":[{"name":"DYT-THAP1","type":"exact"},{"name":"DYT6","type":"exact"},{"name":"THAP1 generalised isolated dystonia","type":"exact"},{"name":"THAP1 generalized isolated dystonia","type":"exact"},{"name":"adolescent-onset dystonia of mixed type","type":"related"},{"name":"dystonia 6","type":"related"},{"name":"dystonia 6, torsion","type":"related"},{"name":"generalised cervical and upper-limb-onset dystonia","type":"exact"},{"name":"generalised isolated dystonia caused by mutation in THAP1","type":"exact"},{"name":"generalized cervical and upper-limb-onset dystonia","type":"exact"},{"name":"generalized isolated dystonia caused by mutation in THAP1","type":"exact"},{"name":"idiopathic torsion dystonia of mixed type","type":"exact"},{"name":"primary dystonia, DYT6 type","type":"related"},{"name":"torsion dystonia adult onset mixed type","type":"related"},{"name":"torsion dystonia type 6","type":"exact"},{"name":"torsion dystonia, adult-onset, mixed type","type":"related"}],"termid":"MONDO:0011264","xrefs":{"Monarch":{"xref_id":"0011264"}}}


id: PATO:0000775
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000775 learning value (obsolete PATO:0000775)","termid":"PATO:0000775"}


id: PBO:0083704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER integral membrane protein, ERMES complex subunit; ERMES links the ER to mitochondria and may promote inter-organellar calcium and phospholipid exchange as well as coordinating mitochondrial DNA replication and growth; required for mitophagy; ERMES complex is often co-localized with peroxisomes and with concentrated areas of pyruvate dehydrogenase","termid":"PBO:0083704"}


id: MONDO:0017054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Thiamine-responsive maple syrup urine disease (thiamine-responsive MSUD) is a less severe variant of MSUD that manifests with a phenotype similar to intermediate MSUD but that responds positively to treatment with thiamine.","definition_xrefs":["Orphanet:268184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maple syrup urine disease","termid":"MONDO:0009563"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"thiamine-responsive maple syrup urine disease","secondary_identifiers":["GARD:17266","UMLS:C0751285","NANDO:2201081","MEDGEN:199627"],"synonyms":[{"name":"thiamine-responsive BCKD deficiency","type":"exact"},{"name":"thiamine-responsive MSUD","type":"exact"},{"name":"thiamine-responsive branched-chain 2-ketoacid dehydrogenase deficiency","type":"exact"},{"name":"thiamine-responsive branched-chain alpha-ketoacid dehydrogenase deficiency","type":"exact"},{"name":"thiamine-responsive maple syrup urine disease","type":"exact"}],"termid":"MONDO:0017054","xrefs":{"Monarch":{"xref_id":"0017054"}}}


id: GO:0021796
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process that results in the creation of areas within the cerebral cortex that will direct the behavior of cell migration and differentiation as the cortex develops.","definition_xrefs":["GOC:dph","GOC:jid","GO_REF:0000021","GOC:cls","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"part_of","term_name":"telencephalon regionalization","termid":"GO:0021978"},{"relation_name":"part_of","term_name":"cerebral cortex development","termid":"GO:0021987"}],"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":"cerebral cortex regionalization","synonyms":[{"name":"cerebral cortex arealization","type":"exact"},{"name":"cerebral cortex pattern biosynthesis","type":"exact"},{"name":"cerebral cortex pattern formation","type":"exact"}],"termid":"GO:0021796"}


id: GO:0032008
data:
  {"annotated_genes":["SJAG_00457","SJAG_06588","SJAG_00143","SJAG_05030","SJAG_00209","SJAG_02424","SJAG_03089","SJAG_00561","SJAG_02605","SJAG_05184","SJAG_03371","SJAG_03405","SJAG_04910","SJAG_04496","SJAG_02231","SJAG_03907"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69614,73381],"is_not":false,"summary":null,"term":"GO:0032008"},{"annotations":[77120,88631,76215,113191,74379,96420,94643,72870,76605,75768,110868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904263"},{"annotations":[91518,107319,98070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904515"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of TOR signaling.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of TOR signaling","termid":"GO:0032006"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"TOR signaling","termid":"GO:0031929"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00143":null,"SJAG_00209":null,"SJAG_00457":null,"SJAG_00561":null,"SJAG_02231":null,"SJAG_02424":null,"SJAG_02605":null,"SJAG_03089":null,"SJAG_03371":null,"SJAG_03405":null,"SJAG_03907":null,"SJAG_04496":null,"SJAG_04910":null,"SJAG_05030":null,"SJAG_05184":null,"SJAG_06588":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of TOR signaling","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"activation of TOR signaling pathway","type":"narrow"},{"name":"positive regulation of TOR signaling cascade","type":"related"},{"name":"positive regulation of TOR signaling pathway","type":"exact"},{"name":"positive regulation of TOR signalling pathway","type":"exact"},{"name":"positive regulation of target of rapamycin signaling pathway","type":"exact"},{"name":"positive regulation of target of rapamycin signalling pathway","type":"exact"},{"name":"stimulation of TOR signaling pathway","type":"narrow"},{"name":"up regulation of TOR signaling pathway","type":"exact"},{"name":"up-regulation of TOR signaling pathway","type":"exact"},{"name":"upregulation of TOR signaling pathway","type":"exact"}],"termid":"GO:0032008","terms_by_termid":{"GO:0032008":null,"GO:1904263":null,"GO:1904515":null}}


id: PR:O74312
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atg9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74312"],"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":"autophagy-related protein 9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC15D4.07c","synonyms":[{"name":"Spom972h-atg9","type":"exact"}],"termid":"PR:O74312"}


id: PBO:0062380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily D member 2","termid":"PBO:0062380"}


id: MONDO:0016808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial DNA depletion syndrome, hepatocerebral form (obsolete MONDO:0016808)","termid":"MONDO:0016808","xrefs":{"Monarch":{"xref_id":"0016808"}}}


id: PBO:0041489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 12 open reading frame 4","termid":"PBO:0041489"}


id: MONDO:0022200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete treatment for disease (obsolete MONDO:0022200)","termid":"MONDO:0022200","xrefs":{"Monarch":{"xref_id":"0022200"}}}


id: PBO:0036398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribose diphosphatase, NudF subfamily Ysa1 (predicted)","termid":"PBO:0036398"}


id: GO:0033739
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7-aminomethyl-7-deazaguanine + 2 NADP+ = 7-cyano-7-deazaguanine + 3 H+ + 2 NADPH.","definition_xrefs":["EC:1.7.1.13","RHEA:13409"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor","termid":"GO:0046857"}],"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:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"preQ1 synthase activity","secondary_identifiers":["KEGG_REACTION:R07605","MetaCyc:RXN0-4022"],"synonyms":[{"name":"7-aminomethyl-7-carbaguanine:NADP+ oxidoreductase activity","type":"exact"},{"name":"7-cyano-7-deazaguanine reductase activity","type":"related"},{"name":"QueF","type":"related"},{"name":"YkvM","type":"related"},{"name":"preQ0 oxidoreductase activity","type":"related"},{"name":"preQ0 reductase activity","type":"related"},{"name":"queuine synthase activity","type":"related"},{"name":"queuine:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0033739"}


id: MONDO:0016445
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial anetoderma is an extremely rare genetic skin disease characterized by loss of elastin tissue leading to localized areas of flaccid skin and a family history of the disorder.","definition_xrefs":["Orphanet:228277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermis disorder","termid":"MONDO:0021154"}],"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":"familial anetoderma","secondary_identifiers":["SCTID:733467001","GARD:20585","UMLS:C4518793","MEDGEN:1387956"],"synonyms":[{"name":"hereditary anetoderma","type":"exact"},{"name":"hereditary macular atrophy","type":"exact"}],"termid":"MONDO:0016445","xrefs":{"Monarch":{"xref_id":"0016445"}}}


id: MOD:01442
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links an L-valine residue and an L-tyrosine residue by an ether bond to form 3-(O4'-L-tyrosyl)-L-valine.","definition_xrefs":["PubMed:19321420","RESID:AA0490"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uncategorized crosslinked residues","termid":"MOD:00692"},{"relation_name":"is_a","term_name":"crosslinked L-tyrosine residue","termid":"MOD:02058"},{"relation_name":"is_a","term_name":"crosslinked L-valine residue","termid":"MOD:02059"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-(O4'-L-tyrosyl)-L-valine","synonyms":[{"name":"(2S)-2-amino-3-(4-[(2S)-2-amino-2-carboxyethyl]phenoxy)-3-methylbutanoic acid","type":"exact"},{"name":"3-(O4'-L-tyrosyl)-L-valine","type":"exact"},{"name":"CROSSLNK 3-(O4'-tyrosyl)-valine (Val-Tyr)","type":"exact"}],"termid":"MOD:01442"}


id: MONDO:0016392
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cerebellar hypoplasia-tapetoretinal degeneration syndrome is a rare syndrome with a cerebellar malformation as a major feature characterized by cerebellar hypoplasia, bilateral retinal pigmentary changes, intellectual disability that can range from mild to moderate and pronounced language development delay. It presents with early developmental delay, central and peripheral non-progressive visual impairment or asymptomatic retinal changes, hypotonia, non-progressive ataxia and nystagmus.","definition_xrefs":["Orphanet:2246"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellar hypoplasia-tapetoretinal degeneration syndrome","secondary_identifiers":["MEDGEN:902621","DOID:0070339","GARD:1196","UMLS:C4275139"],"synonyms":[{"name":"cerebellar hypoplasia tapetoretinal degeneration","type":"related"}],"termid":"MONDO:0016392","xrefs":{"Monarch":{"xref_id":"0016392"}}}


id: PBO:0041470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 11 open reading frame 24","termid":"PBO:0041470"}


id: GO:0046378
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving enterobacterial common antigen, an acidic polysaccharide containing N-acetyl-D-glucosamine, N-acetyl-D-mannosaminouronic acid, and 4-acetamido-4,6-dideoxy-D-galactose. A major component of the cell wall outer membrane of Gram-negative bacteria.","definition_xrefs":["GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide metabolic process","termid":"GO:0005976"},{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"enterobacterial common antigen metabolic process","synonyms":[{"name":"enterobacterial common antigen metabolism","type":"exact"}],"termid":"GO:0046378"}


id: GO:0018733
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3,4-dihydrocoumarin + H2O = 3-(2-hydroxyphenyl) propionate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 3,4-dihydrocoumarin hydrolase activity (obsolete GO:0018733)","termid":"GO:0018733"}


id: GO:1901964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell proliferation involved in outflow tract morphogenesis.","definition_xrefs":["GOC:TermGenie","GOC:mtg_heart","GOC:dph","PMID:21419760"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell proliferation involved in outflow tract morphogenesis","termid":"GO:1901963"},{"relation_name":"is_a","term_name":"positive regulation of cell proliferation involved in heart morphogenesis","termid":"GO:2000138"},{"relation_name":"positively_regulates","term_name":"cell proliferation involved in outflow tract morphogenesis","termid":"GO:0061325"}],"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 proliferation involved in outflow tract morphogenesis","synonyms":[{"name":"activation of cell proliferation involved in outflow tract morphogenesis","type":"narrow"},{"name":"up regulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"},{"name":"up-regulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"},{"name":"upregulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"}],"termid":"GO:1901964"}


id: PR:O74520
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trp663 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74520"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized membrane protein C663.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC663.14c","synonyms":[{"name":"Spom972h-trp663","type":"exact"}],"termid":"PR:O74520"}


id: GO:0016408
data:
  {"annotated_genes":["SJAG_04178","SJAG_04107","SJAG_04972","SJAG_00413","SJAG_02305"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003985"},{"annotations":[59922,58545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004321"},{"annotations":[77188,79218],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004758"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of an acyl group to a carbon atom on the acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00413":null,"SJAG_02305":null,"SJAG_04107":null,"SJAG_04178":null,"SJAG_04972":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016746","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"C-acyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null},"termid":"GO:0016408","terms_by_termid":{"GO:0003985":null,"GO:0004321":null,"GO:0004758":null}}


id: PBO:0084067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase component of U5 snRNP involved in mRNA splicing via spliceosome; binds directly to U5 snRNA; proposed to be involved in conformational changes of the spliceosome; similarity to ribosomal translocation factor EF-2","termid":"PBO:0084067"}


id: PBO:0086045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function involved in prospore membrane assembly; involved in the assembly of the prospore membrane during sporulation; interacts with Spo14p","termid":"PBO:0086045"}


id: GO:0046409
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: shikimate or quinate ester of p-coumaric acid + NADPH + H+ + O2 = caffeic acid conjugate (caffeoyl shikimic acid or chlorogenic acid) + H2O + NADP+.","definition_xrefs":["PMID:11891223","PMID:11429408"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"p-coumarate 3-hydroxylase activity","synonyms":[{"name":"cytochrome P450 CYP98A3","type":"narrow"}],"termid":"GO:0046409"}


id: MONDO:0000027
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epilepsy, absence (obsolete MONDO:0000027)","termid":"MONDO:0000027","xrefs":{"Monarch":{"xref_id":"0000027"}}}


id: PBO:0030644
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_pH","termid":"PBO:0030644"}


id: PBO:0034688
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_curved_vegetative_cell_with_long_curved_cytoplasmic_microtubules","termid":"PBO:0034688"}


id: GO:0070387
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A procollagen-proline 4-dioxygenase complex that contains alpha subunits of the type II isoform; its activity is inhibited by poly(L-proline) only at high concentrations.","definition_xrefs":["PMID:7753822","PMID:14500733"],"direct_ancestors":[{"relation_name":"is_a","term_name":"procollagen-proline 4-dioxygenase complex","termid":"GO:0016222"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005783"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005783","GO:0032991"],"is_obsolete":false,"name":"procollagen-proline 4-dioxygenase complex, alpha(II) type","synonyms":[{"name":"procollagen-proline, 2-oxoglutarate-4-dioxygenase complex, alpha(II) type","type":"exact"},{"name":"prolyl 4-hydroxylase complex (alpha(II)-type)","type":"broad"}],"termid":"GO:0070387"}


id: PBO:0034759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex subunit Ngg1/Ada3","termid":"PBO:0034759"}


id: PBO:0077117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of inner mitochondrial membrane 29","termid":"PBO:0077117"}


id: PBO:0034059
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_start_sequence_of","termid":"PBO:0034059"}


id: PBO:0084960
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Myo-inositol transporter; member of the sugar transporter superfamily; expressed constitutively; ITR2 has a paralog, ITR1, that arose from the whole genome duplication","termid":"PBO:0084960"}


id: GO:0035820
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which angiotensin decreases the amount of sodium that is excreted in urine over a unit of time.","definition_xrefs":["GOC:yaf","GOC:mtg_25march11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of renal output by angiotensin","termid":"GO:0003083"},{"relation_name":"is_a","term_name":"negative regulation of renal sodium excretion","termid":"GO:0035814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of renal sodium excretion by angiotensin","termid":"GO:0035820"}


id: GO:0015645
data:
  {"annotated_genes":["SJAG_00947","SJAG_03471","SJAG_03909"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031956"},{"annotations":[105923,113756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090432"},{"annotations":[105924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090434"},{"annotations":[105925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090433"}]},"cv_name":"molecular_function","definition":"Catalysis of the ligation of a fatty acid to an acceptor, coupled to the hydrolysis of ATP.","definition_xrefs":["GOC:cjk","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-thiol ligase activity","termid":"GO:0016878"},{"relation_name":"is_a","term_name":"ATP-dependent activity","termid":"GO:0140657"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00947":null,"SJAG_03471":null,"SJAG_03909":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016874"],"is_obsolete":false,"name":"fatty acid ligase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"fatty acid CoA ligase activity","type":"related"},{"name":"fatty acyl-coenzyme A synthetase activity","type":"related"},{"name":"fatty-acid ligase activity","type":"exact"}],"termid":"GO:0015645","terms_by_termid":{"GO:0031956":null,"GO:0090432":null,"GO:0090433":null,"GO:0090434":null}}


id: PBO:0072958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCEL antisense RNA 1","termid":"PBO:0072958"}


id: MONDO:0001540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An occupational lung disorder caused by inhalation of bagasse dust. In the acute phase, it manifests as cough, dyspnea, fever, chills, and weakness. Chronic exposure may lead to interstitial lung fibrosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypersensitivity pneumonitis","termid":"MONDO:0017853"}],"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":"bagassosis","secondary_identifiers":["MEDGEN:2539","DOID:12522","MESH:D011009","ICD10CM:J67.1","ICD9:495.1","NCIT:C34409","icd11.foundation:1123061945","UMLS:C0004681","SCTID:67242002"],"synonyms":[{"name":"bagasse extrinsic allergic alveolitis","type":"exact"},{"name":"bagasse workers lung","type":"exact"},{"name":"extrinsic allergic alveolitis from bagasse","type":"exact"},{"name":"sugar cane worker pneumonitis","type":"exact"}],"termid":"MONDO:0001540","xrefs":{"Monarch":{"xref_id":"0001540"}}}


id: PBO:0002547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit Pmc3/Med27","termid":"PBO:0002547"}


id: MONDO:0002924
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm arising from smooth muscle.","definition_xrefs":["NCIT:C6511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle cancer","termid":"MONDO:0005864"},{"relation_name":"is_a","term_name":"smooth muscle tumor","termid":"MONDO:0006975"}],"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":"smooth muscle cancer","secondary_identifiers":["DOID:4230","UMLS:C1334620","MEDGEN:233670"],"synonyms":[{"name":"cancer of smooth muscle","type":"exact"},{"name":"cancer of the smooth muscle","type":"exact"},{"name":"malignant neoplasm of smooth muscle","type":"exact"},{"name":"malignant neoplasm of the smooth muscle","type":"exact"},{"name":"malignant smooth muscle neoplasm","type":"exact"},{"name":"malignant smooth muscle tumor","type":"exact"},{"name":"malignant smooth muscle tumour","type":"exact"},{"name":"malignant tumor of smooth muscle","type":"exact"},{"name":"malignant tumor of the smooth muscle","type":"exact"},{"name":"malignant tumour of smooth muscle","type":"exact"},{"name":"malignant tumour of the smooth muscle","type":"exact"},{"name":"smooth muscle cancer","type":"exact"}],"termid":"MONDO:0002924","xrefs":{"Monarch":{"xref_id":"0002924"}}}


id: PBO:0062869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OTU deubiquitinase 6A","termid":"PBO:0062869"}


id: PBO:0068252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 28S ribosomal N4","termid":"PBO:0068252"}


id: GO:1900594
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving (+)-kotanin.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"(+)-kotanin metabolic process","synonyms":[{"name":"(+)-kotanin metabolism","type":"exact"}],"termid":"GO:1900594"}


id: MONDO:0007039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tumor-prone disorder characterized by the development of multiple schwannomas and meningiomas.","definition_xrefs":["Orphanet:637"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibromatosis","termid":"MONDO:0021061"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"NF2-related schwannomatosis","secondary_identifiers":["ICD10CM:Q85.02","MEDGEN:18014","OMIM:101000","DOID:0111252","MESH:D009464","SCTID:92503002","MedDRA:10029271","UMLS:C0027832","GARD:7193","MedDRA:10000523","ICD9:237.72","NANDO:1200227","NCIT:C3274","icd11.foundation:14808714"],"synonyms":[{"name":"NF2","type":"exact"},{"name":"NF2-related schwannomatosis","type":"exact"},{"name":"SWNV","type":"exact"},{"name":"acoustic Schwannomas, bilateral","type":"related"},{"name":"acoustic neurinoma bilateral","type":"related"},{"name":"acoustic neurinoma, bilateral","type":"related"},{"name":"acoustic neurofibromatosis","type":"broad"},{"name":"acoustic schwannomas bilateral","type":"related"},{"name":"bilateral acoustic neurofibromatosis","type":"exact"},{"name":"central neurofibromatosis","type":"exact"},{"name":"full NF2","type":"exact"},{"name":"full neurofibromatosis type 2","type":"exact"},{"name":"neurofibromatosis 2","type":"exact"},{"name":"neurofibromatosis central type","type":"related"},{"name":"neurofibromatosis type 2","type":"exact"},{"name":"neurofibromatosis type II","type":"related"},{"name":"neurofibromatosis, central type","type":"related"},{"name":"neurofibromatosis, type 2","type":"related"},{"name":"neurofibromatosis, type II","type":"related"},{"name":"nonmosaic NF2-related schwannomatosis","type":"exact"},{"name":"nonmosaic neurofibromatosis type 2","type":"exact"},{"name":"vestibular schwannomatosis","type":"exact"}],"termid":"MONDO:0007039","xrefs":{"Monarch":{"xref_id":"0007039"}}}


id: PBO:0039225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldo-keto reductase family 7 like (gene/pseudogene)","termid":"PBO:0039225"}


id: PBO:0052167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium inwardly rectifying channel subfamily J member 15","termid":"PBO:0052167"}


id: PBO:0076374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TGF-beta activated kinase 1 (MAP3K7) binding protein 2","termid":"PBO:0076374"}


id: MONDO:0016299
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A central nervous system malformation syndrome characterized by holoprosencephaly with microcephaly, abnormal eye morphology (hypotelorism, cyclopia, exophthalmos), nasal anomalies (single nostril or absent nose), and cleft lip/palate, combined with signs of caudal regression (sacral agenesis, sirenomelia with absent external genitalia).","definition_xrefs":["Orphanet:2165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"holoprosencephaly-caudal dysgenesis syndrome","secondary_identifiers":["UMLS:C4749731","GARD:2722","MEDGEN:1653112","ICD10CM:Q04.2"],"termid":"MONDO:0016299","xrefs":{"Monarch":{"xref_id":"0016299"}}}


id: PBO:0027053
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_curved_vegetative_cell_with_long_curved_microtubules","termid":"PBO:0027053"}


id: MONDO:0016684
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anaplastic astrocytoma is a rare, high-grade, malignant glial tumor, histologically characterized by abundance of pleomorphic astrocytes and multiple mitotic figures, often associated with diffuse infiltration of the surrounding tissue, considerable edema and mass effect and involvement of the contralateral brain. Depending on the primary localization of the tumor, patients can present with signs of raised intracranial pressure (headache, vomiting, papilledema), seizures, progressive neurological deficits, and/or behavioral changes. The tumor is most commonly localized in the frontal and temporal lobes, brain stem and spinal cord.","definition_xrefs":["Orphanet:251589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"high grade astrocytic tumor","termid":"MONDO:0016680"},{"relation_name":"is_a","term_name":"astrocytoma (excluding glioblastoma)","termid":"MONDO:0019781"},{"relation_name":"is_a","term_name":"anaplastic cancer","termid":"MONDO:0020633"}],"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":"anaplastic astrocytoma","secondary_identifiers":["EFO:0002499","ICDO:9401/3","MedDRA:10060971","MEDGEN:137784","NORD:769","ONCOTREE:AASTR","NCIT:C9477","DOID:3078","UMLS:C0334579","GARD:5860","MedDRA:10002224","NANDO:2200086"],"synonyms":[{"name":"anaplastic astrocytoma","type":"exact"},{"name":"astrocytoma, anaplastic, malignant","type":"exact"},{"name":"grade III astrocytic neoplasm","type":"exact"},{"name":"grade III astrocytic tumor","type":"exact"},{"name":"grade III astrocytic tumour","type":"exact"},{"name":"grade III astrocytoma","type":"exact"},{"name":"malignant astrocytoma","type":"exact"}],"termid":"MONDO:0016684","xrefs":{"Monarch":{"xref_id":"0016684"}}}


id: PBO:0071165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 4","termid":"PBO:0071165"}


id: PBO:0082577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chitin transglycosylase; functions in the transfer of chitin to beta(1-6) and beta(1-3) glucans in the cell wall; similar to and functionally redundant with Crh1; glycosylphosphatidylinositol (GPI)-anchored protein localized to bud neck","termid":"PBO:0082577"}


id: GO:0035799
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for the ureter to attain its fully functional state. The ureter is a muscular tube that transports urine from the kidney to the urinary bladder or from the Malpighian tubule to the hindgut.","definition_xrefs":["GOC:yaf","GOC:bf","PMID:17881463","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ maturation","termid":"GO:0048799"},{"relation_name":"part_of","term_name":"ureter development","termid":"GO:0072189"}],"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":"ureter maturation","termid":"GO:0035799"}


id: PBO:0079296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin tyrosine ligase like 13","termid":"PBO:0079296"}


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


id: MONDO:0011316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteosclerotic chondrodysplasia, lethal, with intracellular inclusions","secondary_identifiers":["MEDGEN:350298","OMIM:603393","UMLS:C1863920","MESH:C566378"],"synonyms":[{"name":"osteosclerotic chondrodysplasia, lethal, with intracellular inclusions","type":"exact"}],"termid":"MONDO:0011316","xrefs":{"Monarch":{"xref_id":"0011316"}}}


id: PBO:0042696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chymotrypsin like elastase 2B","termid":"PBO:0042696"}


id: PR:Q9HDX8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An L-gulonolactone oxidase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-arabinono-1,4-lactone oxidase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB1A10.12c","secondary_identifiers":["UniProtKB:Q9HDX8"],"synonyms":[{"name":"ALO (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"L-galactono-gamma-lactone oxidase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAPB1A10.12c","type":"related"},{"name":"Spom972h-Gulo","type":"exact"}],"termid":"PR:Q9HDX8"}


id: PBO:0047186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 204 member B, pseudogene","termid":"PBO:0047186"}


id: MONDO:0024546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary hypertrophic osteoarthropathy in which the cause of the disease is a mutation in the HPGD gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary hypertrophic osteoarthropathy","termid":"MONDO:0016620"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrophic osteoarthropathy, primary, autosomal recessive, 1","secondary_identifiers":["GARD:15216","MEDGEN:1641972","OMIM:259100","UMLS:C4551679"],"synonyms":[{"name":"Cranioosteoarthropathy","type":"related"},{"name":"Currarino idiopathic osteoarthropathy","type":"related"},{"name":"HPGD primary hypertrophic osteoarthropathy","type":"exact"},{"name":"PDP, autosomal recessive","type":"related"},{"name":"PHOAR1","type":"related"},{"name":"Pho, autosomal recessive","type":"related"},{"name":"Touraine-Solente-Gole syndrome","type":"related"},{"name":"familial idiopathic osteoarthropathy of childhood","type":"related"},{"name":"hypertrophic osteoarthropathy, primary, autosomal recessive 1","type":"exact"},{"name":"hypertrophic osteoarthropathy, primary, autosomal recessive, 1","type":"exact"},{"name":"pachydermoperiostosis, autosomal recessive","type":"related"},{"name":"primary hypertrophic osteoarthropathy caused by mutation in HPGD","type":"exact"}],"termid":"MONDO:0024546","xrefs":{"Monarch":{"xref_id":"0024546"}}}


id: MONDO:0957815
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmental delay with or without epilepsy","secondary_identifiers":["UMLS:C5882702","MEDGEN:1848555","OMIM:620540"],"termid":"MONDO:0957815","xrefs":{"Monarch":{"xref_id":"0957815"}}}


id: GO:0014055
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of acetylcholine by a cell. The acetylcholine acts as a neurotransmitter that acts in both the peripheral nervous system (PNS) and central nervous system (CNS).","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter secretion","termid":"GO:0007269"},{"relation_name":"is_a","term_name":"acetylcholine secretion","termid":"GO:0061526"},{"relation_name":"part_of","term_name":"synaptic transmission, cholinergic","termid":"GO:0007271"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"acetylcholine secretion, neurotransmission","termid":"GO:0014055"}


id: PBO:0047277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FA complementation group D2","termid":"PBO:0047277"}


id: PBO:0078760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase subunit 11-2 pseudogene 3","termid":"PBO:0078760"}


id: GO:0021930
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of neuroblasts that will give rise to granule cells. A granule cell is a glutamatergic interneuron found in the cerebellar cortex.","definition_xrefs":["GOC:cls","GO_REF:0000021","GOC:dph","GOC:jid","GOC:dgh","PMID:15157725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell proliferation in external granule layer","termid":"GO:0021924"}],"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":"cerebellar granule cell precursor proliferation","termid":"GO:0021930"}


id: RO:0002559
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"causal_relation_between_material_entities","termid":"RO:0002506"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causally_influenced_by","termid":"RO:0002559"}


id: GO:0046235
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of gallate, the anion of gallic acid (3,4,5-trihydroxybenzoic acid).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete gallate biosynthetic process (obsolete GO:0046235)","synonyms":[{"name":"gallate anabolism","type":"exact"},{"name":"gallate biosynthesis","type":"exact"},{"name":"gallate formation","type":"exact"},{"name":"gallate synthesis","type":"exact"},{"name":"gallic acid biosynthesis","type":"exact"},{"name":"gallic acid biosynthetic process","type":"exact"}],"termid":"GO:0046235"}


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


id: PBO:0084819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein of unknown function; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0084819"}


id: GO:1905717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cornification.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:26014679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of programmed cell death","termid":"GO:0043068"},{"relation_name":"is_a","term_name":"regulation of cornification","termid":"GO:1905715"},{"relation_name":"positively_regulates","term_name":"cornification","termid":"GO:0070268"}],"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 cornification","synonyms":[{"name":"activation of cornification","type":"narrow"},{"name":"up regulation of cornification","type":"exact"},{"name":"up-regulation of cornification","type":"exact"},{"name":"upregulation of cornification","type":"exact"}],"termid":"GO:1905717"}


id: GO:1901810
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving beta-carotene.","definition_xrefs":["GOC:yaf","PMID:11387982","UniPathway:UPA00802","GOC:TermGenie","MetaCyc:PWY-5943"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid metabolic process","termid":"GO:0016116"},{"relation_name":"is_a","term_name":"carotene metabolic process","termid":"GO:0016119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"beta-carotene metabolic process","synonyms":[{"name":"beta-carotene metabolism","type":"exact"}],"termid":"GO:1901810"}


id: GO:0009211
data:
  {"annotated_genes":["SJAG_04627","SJAG_04487","SJAG_04657","SJAG_04665","SJAG_00885"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68976,92762,71357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006235"},{"annotations":[79787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046081"},{"annotations":[107581],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009212"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving pyrimidine deoxyribonucleoside triphosphate, a compound consisting of a pyrimidine base linked to a deoxyribose sugar esterified with triphosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside triphosphate metabolic process","termid":"GO:0009147"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00885":null,"SJAG_04487":null,"SJAG_04627":null,"SJAG_04657":null,"SJAG_04665":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"pyrimidine deoxyribonucleoside triphosphate metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"pyrimidine deoxyribonucleoside triphosphate metabolism","type":"exact"}],"termid":"GO:0009211","terms_by_termid":{"GO:0006235":null,"GO:0009212":null,"GO:0046081":null}}


id: PBO:0034187
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_orthology_relationship_with","termid":"PBO:0034187"}


id: GO:0060277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stop, prevents or decreases transcription as part of the G1 phase of the mitotic cell cycle.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transcription involved in G1 phase of mitotic cell cycle (obsolete GO:0060277)","synonyms":[{"name":"negative regulation of transcription from RNA polymerase II promoter during G1 phase of mitotic cell cycle","type":"related"},{"name":"negative regulation of transcription involved in G1 phase of mitotic cell cycle","type":"exact"}],"termid":"GO:0060277"}


id: PBO:0084845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the large subunit; homolog of human Bcl-2 interacting protein BMRP","termid":"PBO:0084845"}


id: MONDO:0000060
data:
  {"annotated_genes":["SJAG_02246"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008872"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"microcephaly","termid":"MONDO:0001149"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02246":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"microcephalic osteodysplastic primordial dwarfism","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0000060","terms_by_termid":{"MONDO:0008872":null},"xrefs":{"Monarch":{"xref_id":"0000060"}}}


id: PBO:0059339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MRPS9 antisense RNA 1","termid":"PBO:0059339"}


id: FYPO:0001015
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 phosphatidylinositol-4-phosphate measured in a cell differs from normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered cellular phosphoinositide level","termid":"FYPO:0001290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"altered cellular phosphatidylinositol-4-phosphate level","synonyms":[{"name":"abnormal cellular phosphatidylinositol-4-phosphate level","type":"exact"},{"name":"altered PI-4-P accumulation","type":"related"},{"name":"altered cellular PI(4)P level","type":"exact"},{"name":"altered cellular PI-4-P level","type":"exact"},{"name":"altered cellular phosphatidylinositol-4-phosphate level during mitotic cell cycle","type":"related"},{"name":"altered cellular phosphatidylinositol-4-phosphate level during vegetative growth","type":"exact"}],"termid":"FYPO:0001015"}


id: MONDO:0005304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm that involves the biliary tract.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biliary tract disorder","termid":"MONDO:0004868"},{"relation_name":"is_a","term_name":"liver and intrahepatic bile duct neoplasm","termid":"MONDO:0024477"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"biliary tract neoplasm","secondary_identifiers":["DOID:0050625","EFO:0003891","HP:0100574","MEDGEN:14118","SCTID:126853008","ONCOTREE:BILIARYTRACT","UMLS:C0005426"],"synonyms":[{"name":"biliary tract neoplasm","type":"exact"},{"name":"biliary tract neoplasm (disease)","type":"exact"},{"name":"biliary tree neoplasm","type":"exact"},{"name":"biliary tree neoplasm (disease)","type":"exact"},{"name":"biliary tree tumor","type":"exact"},{"name":"biliary tree tumour","type":"exact"},{"name":"neoplasm of biliary tree","type":"exact"},{"name":"neoplasm of extrahepatic bile ducts","type":"exact"},{"name":"tumor of biliary tree","type":"exact"},{"name":"tumour of biliary tree","type":"exact"},{"name":"tumour of the extrahepatic bile duct","type":"related"}],"termid":"MONDO:0005304","xrefs":{"Monarch":{"xref_id":"0005304"}}}


id: GO:0071126
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaV-beta6 integrin complex bound to osteopontin.","definition_xrefs":["PMID:16005200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"alphaV-beta6 integrin-osteopontin complex","synonyms":[{"name":"ITGAV-ITGB6-SPP1 complex","type":"narrow"}],"termid":"GO:0071126"}


id: GO:0052576
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The accumulation and maintenance in cells or tissues of carbohydrates, any of a group of organic compounds based of the general formula Cx(H2O)y.","definition_xrefs":["PMID:10758476"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate localization","termid":"GO:0052575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"carbohydrate storage","termid":"GO:0052576"}


id: PR:O13835
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U3 small nucleolar ribonucleoprotein protein IMP3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11831:SF1","OMA:SCHPO02165"],"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":"U3 small nucleolar ribonucleoprotein protein imp3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19D5.05c","secondary_identifiers":["UniProtKB:O13835"],"synonyms":[{"name":"Spom972h-IMP3","type":"exact"},{"name":"U3 snoRNP protein imp3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13835"}


id: GO:1900344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of methane biosynthetic process from dimethyl sulfide.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of sulfur metabolic process","termid":"GO:0051176"},{"relation_name":"is_a","term_name":"regulation of methane biosynthetic process from dimethyl sulfide","termid":"GO:1900342"},{"relation_name":"is_a","term_name":"positive regulation of alkane biosynthetic process","termid":"GO:1901579"},{"relation_name":"is_a","term_name":"positive regulation of cellular respiration","termid":"GO:1901857"},{"relation_name":"positively_regulates","term_name":"methane biosynthetic process from dimethyl sulfide","termid":"GO:2001131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"positively_regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0006091"],"is_obsolete":false,"name":"positive regulation of methane biosynthetic process from dimethyl sulfide","synonyms":[{"name":"activation of methane biosynthetic process from dimethyl sulfide","type":"narrow"},{"name":"up regulation of methane biosynthetic process from dimethyl sulfide","type":"exact"},{"name":"up-regulation of methane biosynthetic process from dimethyl sulfide","type":"exact"},{"name":"upregulation of methane biosynthetic process from dimethyl sulfide","type":"exact"}],"termid":"GO:1900344"}


id: PBO:0028776
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ubiquitinyl_hydrolase_activity","termid":"PBO:0028776"}


id: PR:O36033
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tetratricopeptide repeat protein 27 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02024","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":"TPR repeat-containing protein C19B12.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19B12.01","secondary_identifiers":["UniProtKB:O36033"],"synonyms":[{"name":"Spom972h-TTC27","type":"exact"}],"termid":"PR:O36033"}


id: MONDO:0014983
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the SLC18A3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myasthenic syndrome","termid":"MONDO:0018940"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital myasthenic syndrome 21","secondary_identifiers":["GARD:16212","MEDGEN:934621","UMLS:C4310654","DOID:0110672","OMIM:617239"],"synonyms":[{"name":"CMS21","type":"exact"},{"name":"SLC18A3 congenital myasthenic syndrome","type":"exact"},{"name":"congenital myasthenic syndrome 21, presynaptic","type":"exact"},{"name":"congenital myasthenic syndrome caused by mutation in SLC18A3","type":"exact"},{"name":"congenital myasthenic syndrome type 21","type":"exact"},{"name":"myasthenic syndrome, congenital, 21, presynaptic","type":"exact"}],"termid":"MONDO:0014983","xrefs":{"Monarch":{"xref_id":"0014983"}}}


id: PBO:0014614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"antisense RNA complementary to adh1, major transcript","termid":"PBO:0014614"}


id: PBO:0065855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB12, member RAS oncogene family","termid":"PBO:0065855"}


id: PBO:0043491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centlein","termid":"PBO:0043491"}


id: MONDO:0020217
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete secondary dysgenetic glaucoma associated with neural crest cell migration anomaly (obsolete MONDO:0020217)","secondary_identifiers":["Orphanet:98632"],"synonyms":[{"name":"glaucoma associated with neural crest cell migration anomaly","type":"related"}],"termid":"MONDO:0020217","xrefs":{"Monarch":{"xref_id":"0020217"}}}


id: PBO:0109297
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"codon-optimization decreases protein concentration","termid":"PBO:0109297"}


id: PBO:0046848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid binding protein 9","termid":"PBO:0046848"}


id: PBO:0109607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A15","termid":"PBO:0109607"}


id: PBO:0029688
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_hydrogen_peroxide-induced_proteins_during_vegetative_growth","termid":"PBO:0029688"}


id: MONDO:0019014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mutilating palmoplantar keratoderma with periorificial keratotic plaques (obsolete MONDO:0019014)","termid":"MONDO:0019014","xrefs":{"Monarch":{"xref_id":"0019014"}}}


id: PBO:0065167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein C receptor","termid":"PBO:0065167"}


id: PBO:0044138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTBP2 pseudogene 4","termid":"PBO:0044138"}


id: GO:0004971
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"An ionotropic glutamate receptor activity that exhibits fast gating by glutamate and acts by opening a cation channel permeable to sodium, potassium, and, in the absence of a GluR2 subunit, calcium.","definition_xrefs":["GOC:mah","PMID:8804111","PMID:10049997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamate-gated receptor activity","termid":"GO:0004970"},{"relation_name":"is_a","term_name":"inorganic cation transmembrane transporter activity","termid":"GO:0022890"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"AMPA glutamate receptor activity","synonyms":[{"name":"AMPA receptor activity","type":"exact"},{"name":"alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate selective glutamate receptor activity","type":"exact"}],"termid":"GO:0004971"}


id: PBO:0006832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin-like protein, Ino80 complex subunit Arp8","termid":"PBO:0006832"}


id: PBO:0058447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5047","termid":"PBO:0058447"}


id: MONDO:0011634
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign myopathy with symptoms and signs of muscular hyperexcitability. The typical finding is electrically silent muscle contractions provoked by mechanical stimuli and stretch","definition_xrefs":["doi:10.1002/mus.10156"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"rippling muscle disease","secondary_identifiers":["MedDRA:10069417","icd11.foundation:894802822","ICD9:359.29","MEDGEN:342944","UMLS:C1853698","SCTID:709281006"],"termid":"MONDO:0011634","xrefs":{"Monarch":{"xref_id":"0011634"}}}


id: FYPO:0008278
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 5-diphospho-1D-myo-inositol 1,2,3,4,6-pentakisphosphate (5-IP7) is higher than normal.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular myo-inositol level","termid":"FYPO:0006950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular 5-IP7 level","termid":"FYPO:0008278"}


id: GO:0070596
data:
  {"annotated_genes":["SJAG_02916","SJAG_02278","SJAG_04236","SJAG_03057","SJAG_00424","SJAG_04666","SJAG_00610","SJAG_04184","SJAG_01028"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78988,71796,70974,73738,73920],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070600"},{"annotations":[92750,89761,103167,95266],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0070610"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (1->3)-alpha-D-glucans, compounds composed of glucose residues linked by (1->3)-alpha-D-glucosidic bonds.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-glucan biosynthetic process","termid":"GO:0030979"},{"relation_name":"is_a","term_name":"(1->3)-alpha-glucan metabolic process","termid":"GO:0070595"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00424":null,"SJAG_00610":null,"SJAG_01028":null,"SJAG_02278":null,"SJAG_02916":null,"SJAG_03057":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04666":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"(1->3)-alpha-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"1,3-alpha-glucan anabolism","type":"exact"},{"name":"1,3-alpha-glucan biosynthesis","type":"exact"},{"name":"1,3-alpha-glucan biosynthetic process","type":"exact"},{"name":"1,3-alpha-glucan formation","type":"exact"},{"name":"1,3-alpha-glucan synthesis","type":"exact"},{"name":"alpha-1,3 glucan anabolism","type":"exact"},{"name":"alpha-1,3 glucan biosynthesis","type":"exact"},{"name":"alpha-1,3 glucan biosynthetic process","type":"exact"},{"name":"alpha-1,3 glucan formation","type":"exact"},{"name":"alpha-1,3 glucan synthesis","type":"exact"}],"termid":"GO:0070596","terms_by_termid":{"GO:0070600":null,"GO:0070610":null}}


id: MONDO:0009564
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Marden-Walker syndrome (MWS) is a malformation syndrome characterized by multiple joint contractures (arthrogryposis), a mask-like face with blepharophimosis, micrognathia, high-arched or cleft palate, low-set ears, decreased muscular bulk, kyphoscoliosis and arachnodactyly.","definition_xrefs":["Orphanet:2461"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome or malformation associated with head and neck malformations (obsolete MONDO:0015501)","termid":"MONDO:0015501"},{"relation_name":"is_a","term_name":"ciliopathy","termid":"MONDO:0005308"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Marden-Walker syndrome","secondary_identifiers":["NORD:1402","icd11.foundation:1983460876","MEDGEN:163206","SCTID:449824004","ICD9:759.89","GARD:6973","MESH:C535910","OMIM:248700","UMLS:C0796033"],"synonyms":[{"name":"MARDEN-WALKER syndrome","type":"related"},{"name":"MWKS","type":"related"},{"name":"Marden Walker Syndrome","type":"exact"},{"name":"Marden-Walker syndrome","type":"exact"},{"name":"Mws","type":"related"},{"name":"connective tissue disorder Marden Walker type","type":"related"}],"termid":"MONDO:0009564","xrefs":{"Monarch":{"xref_id":"0009564"}}}


id: GO:0038156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-3 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:signaling","GOC:nhn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"interleukin-3-mediated signaling pathway","synonyms":[{"name":"IL-3-mediated signaling pathway","type":"exact"},{"name":"interleukin-3-mediated signalling pathway","type":"exact"}],"termid":"GO:0038156"}


id: GO:0071680
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an indole-3-methanol stimulus.","definition_xrefs":["GOC:yaf","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to alcohol","termid":"GO:0097305"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to indole-3-methanol","synonyms":[{"name":"response to indole-3-carbinol","type":"exact"}],"termid":"GO:0071680"}


id: MONDO:0020366
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A developmental glaucoma that results from the abnormal development of the aqueous drainage structure, characterized by an elevated intra-ocular pressure, enlargement of globe (buphthalmos), corneal edema and optic nerve cupping, and presenting clinically with the characteristic triad of epiphora, photophobia and blepharospasm.","definition_xrefs":["Orphanet:98976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary glaucoma","termid":"MONDO:0018174"}],"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 glaucoma","secondary_identifiers":["NCIT:C50648","SCTID:204113001","UMLS:C0020302","ICD9:743.2","ICD9:743.20","DOID:11212","MEDGEN:42532","MESH:D006871"],"synonyms":[{"name":"Buphthalmus","type":"exact"},{"name":"buphthalmia","type":"exact"},{"name":"buphthalmos","type":"exact"},{"name":"hydrophthalmos","type":"exact"},{"name":"primary congenital glaucoma","type":"narrow"}],"termid":"MONDO:0020366","xrefs":{"Monarch":{"xref_id":"0020366"}}}


id: FYPO:0003419
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of malate dehydrogenase (decarboxylating) (NAD+) activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal malate dehydrogenase (decarboxylating) (NAD+) activity","termid":"FYPO:0002621"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000707","FYPO:0000652","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"increased malate dehydrogenase (decarboxylating) (NAD+) activity","synonyms":[{"name":"increased 'malic' enzyme activity","type":"related"},{"name":"increased (S)-malate:NAD+ oxidoreductase (oxaloacetate-decarboxylating) activity","type":"exact"},{"name":"increased NAD-linked malic enzyme activity","type":"related"},{"name":"increased NAD-malic enzyme activity","type":"broad"},{"name":"increased NAD-specific malic enzyme activity","type":"related"},{"name":"increased malate dehydrogenase (oxaloacetate-decarboxylating) activity","type":"exact"}],"termid":"FYPO:0003419"}


id: PBO:0005402
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.1.1.37","termid":"PBO:0005402"}


id: MONDO:0010152
data:
  {"annotated_genes":["SJAG_04110"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87287],"is_not":false,"summary":null,"term":"MONDO:0010152"}]},"cv_name":"mondo","definition":"Trichomegaly-retina pigmentary degeneration-dwarfism syndrome, also known as Oliver-McFarlane syndrome, is an extremely rare genetic disorder characterized by hair abnormalities, severe chorioretinal atrophy, hypopituitarism, short stature, and intellectual disability.","definition_xrefs":["Orphanet:3363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04110":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"trichomegaly-retina pigmentary degeneration-dwarfism syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:719944006","MEDGEN:338532","UMLS:C1848745","DOID:0111271","GARD:5266","MESH:C536554","OMIM:275400"],"synonyms":[{"name":"OMCS","type":"related"},{"name":"Oliver McFarlane syndrome","type":"related"},{"name":"Oliver-McFarlane syndrome","type":"exact"},{"name":"eyelashes, long with intellectual disability","type":"related"},{"name":"eyelashes, long, with intellectual disability","type":"related"},{"name":"eyelashes, long, with mental retardation","type":"related"},{"name":"long eyelashes-intellectual disability syndrome","type":"exact"},{"name":"trichomegaly with intellectual disability, dwarfism and pigmentary degeneration of retina","type":"related"},{"name":"trichomegaly with intellectual disability, dwarfism, and pigmentary Degeneration of retina","type":"related"},{"name":"trichomegaly with mental retardation, dwarfism, and pigmentary Degeneration of retina","type":"related"}],"termid":"MONDO:0010152","terms_by_termid":{"MONDO:0010152":null},"xrefs":{"Monarch":{"xref_id":"0010152"}}}


id: PBO:0013838
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PhosphoPantothenate-Cysteine","termid":"PBO:0013838"}


id: GO:0034781
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: N-cyclohexylformamide + OH- = cyclohexylamine + formate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete N-cyclohexylformamide amidohydrolase activity (obsolete GO:0034781)","termid":"GO:0034781"}


id: PBO:0084655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Minor sphingoid long-chain base kinase; possibly involved in synthesis of long-chain base phosphates, which function as signaling molecules; LCB5 has a paralog, LCB4, that arose from the whole genome duplication","termid":"PBO:0084655"}


id: PR:000027580
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A fungal histone H3.2, initiator methionine removed form in Schizosaccharomyces pombe.","definition_xrefs":["PMID:20929775","PomBase:MAH","PMID:11242054"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3.2 (Schizosaccharomyces pombe)","termid":"PR:000027572"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.2, initiator methionine removed form (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC8D2.04","synonyms":[{"name":"Spom-hht2/InitMet-","type":"exact"}],"termid":"PR:000027580"}


id: PBO:0026727
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_kinetochore_during_mitosis","termid":"PBO:0026727"}


id: GO:0060278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ovulation, the release of a mature ovum/oocyte from an ovary.","definition_xrefs":["GOC:kmv","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"ovulation","termid":"GO:0030728"}],"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 ovulation","termid":"GO:0060278"}


id: PBO:0110501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TGFBR1 pseudogene 1","termid":"PBO:0110501"}


id: GO:1904367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chemokinesis.","definition_xrefs":["GOC:TermGenie","PMID:8679543","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to external stimulus","termid":"GO:0032103"},{"relation_name":"is_a","term_name":"regulation of chemokinesis","termid":"GO:1904365"},{"relation_name":"positively_regulates","term_name":"chemokinesis","termid":"GO:0042466"}],"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 chemokinesis","synonyms":[{"name":"activation of chemokinesis","type":"narrow"},{"name":"up regulation of chemokinesis","type":"exact"},{"name":"up-regulation of chemokinesis","type":"exact"},{"name":"upregulation of chemokinesis","type":"exact"}],"termid":"GO:1904367"}


id: PBO:0040706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 like 12","termid":"PBO:0040706"}


id: PBO:0030114
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_tRNA_processing","termid":"PBO:0030114"}


id: FYPO:0002638
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the mitotic spindle assembly checkpoint is activated more frequently than normal, typically under conditions that do not cause checkpoint activation in wild-type cells. The mitotic spindle assembly checkpoint normally delays the metaphase/anaphase transition of a mitotic nuclear division until the spindle is correctly assembled and chromosomes are attached to the spindle.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic spindle assembly checkpoint","termid":"FYPO:0000168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0000002","FYPO:0000298","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased activation of mitotic spindle assembly checkpoint","synonyms":[{"name":"activation of mitotic spindle assembly checkpoint increased","type":"exact"},{"name":"increased Bub1 foci","type":"related"},{"name":"increased Mad2 foci","type":"related"},{"name":"increased activation of mitotic cell cycle spindle assembly checkpoint","type":"exact"},{"name":"increased mitotic cell cycle spindle assembly checkpoint activation","type":"exact"}],"termid":"FYPO:0002638"}


id: MONDO:0011476
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Immunodeficiency by defective expression of HLA class 1 is a very rare, primary, genetic, immunodeficiency disorder characterized by partial or complete absence of human leukocyte antigen class I expression resulting in a non-specific clinical picture of impaired immune response and susceptibility to infections.","definition_xrefs":["Orphanet:34592"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"severe combined immunodeficiency","termid":"MONDO:0015974"},{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"combined immunodeficiency","termid":"MONDO:0015131"}],"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":"MHC class I deficiency","secondary_identifiers":["NANDO:2200701","OMIMPS:604571","UMLS:C1858266","SCTID:725136003","NANDO:1200328","MEDGEN:346868","DOID:0060009","GARD:8427","icd11.foundation:489749747"],"synonyms":[{"name":"BARE lymphocyte syndrome, type I","type":"related"},{"name":"BLS type 1","type":"related"},{"name":"BLS, type I","type":"exact"},{"name":"BLSI","type":"exact"},{"name":"Bare lymphocyte syndrome type 1","type":"exact"},{"name":"Bare lymphocyte syndrome, type 1","type":"related"},{"name":"Bls, type 1","type":"related"},{"name":"HLA CLASS I deficiency","type":"exact"},{"name":"HLA Class 1 deficiency","type":"related"},{"name":"bare lymphocyte syndrome type I","type":"exact"},{"name":"immunodeficiency by defective expression of HLA class 1","type":"exact"},{"name":"immunodeficiency by defective expression of HLA class type 1","type":"exact"}],"termid":"MONDO:0011476","xrefs":{"Monarch":{"xref_id":"0011476"}}}


id: PBO:0062292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily M member 3","termid":"PBO:0062292"}


id: MONDO:0018506
data:
  {"annotated_genes":["SJAG_00260","SJAG_03920"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87131,87132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011719"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"small intestine neoplasm","termid":"MONDO:0004251"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_03920":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"mesenchymal tumor of small intestine","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:21761","UMLS:C5680077","MEDGEN:1843104","Orphanet:423798"],"synonyms":[{"name":"mesenchymal tumor of small bowel","type":"exact"},{"name":"mesenchymal tumour of small bowel","type":"exact"}],"termid":"MONDO:0018506","terms_by_termid":{"MONDO:0011719":null},"xrefs":{"Monarch":{"xref_id":"0018506"}}}


id: PBO:0051131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 2-70","termid":"PBO:0051131"}


id: PBO:0116995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTDC1 antisense RNA 1","termid":"PBO:0116995"}


id: PBO:0078209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 7-2","termid":"PBO:0078209"}


id: PBO:0028819
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_chromatin_at_replication_forks_during_cellular_response_to_hydroxyurea","termid":"PBO:0028819"}


id: GO:0033972
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: amidinoproclavaminate + H2O = proclavaminate + urea.","definition_xrefs":["EC:3.5.3.22","RHEA:17001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines","termid":"GO:0016813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"proclavaminate amidinohydrolase activity","secondary_identifiers":["MetaCyc:3.5.3.22-RXN","KEGG_REACTION:R05357"],"synonyms":[{"name":"PAH","type":"related"},{"name":"proclavaminate amidino hydrolase activity","type":"related"},{"name":"proclavaminic acid amidino hydrolase activity","type":"related"}],"termid":"GO:0033972"}


id: GO:0031044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The stepwise addition of carbohydrate or carbohydrate derivative residues to the initially added O-linked residue (usually GalNAc) to form the core 8 O-glycan structure, Gal-alpha-(1->3)-GalNAc.","definition_xrefs":["GOC:mah","GOC:pr","PMID:10580130"],"gene_count":0,"genotype_count":0,"name":"obsolete O-glycan processing, core 8 (obsolete GO:0031044)","termid":"GO:0031044"}


id: MONDO:1012763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuroaxonal dystrophy that occurs in dogs due to a mutation in the TECPR2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"neuroaxonal dystrophy, dog","termid":"MONDO:1011561"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroaxonal dystrophy, TECPR2-related, dog","secondary_identifiers":["OMIA:001975-9615"],"termid":"MONDO:1012763","xrefs":{"Monarch":{"xref_id":"1012763"}}}


id: GO:1904328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of myofibroblast contraction.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:19239477"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament-based movement","termid":"GO:1903115"},{"relation_name":"regulates","term_name":"myofibroblast contraction","termid":"GO:1990764"}],"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 myofibroblast contraction","synonyms":[{"name":"regulation of MF contraction","type":"exact"},{"name":"regulation of MFB contraction","type":"exact"}],"termid":"GO:1904328"}


id: PBO:0071709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 7","termid":"PBO:0071709"}


id: PBO:0040912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 16","termid":"PBO:0040912"}


id: GO:0016577
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histones by removal of methyl groups.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete histone demethylation (obsolete GO:0016577)","termid":"GO:0016577"}


id: PBO:0058842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8071-2","termid":"PBO:0058842"}


id: PBO:0116709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily J member 3 (gene/pseudogene)","termid":"PBO:0116709"}


id: PBO:0073992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 2","termid":"PBO:0073992"}


id: MONDO:0011289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apraxia of eyelid opening","secondary_identifiers":["UMLS:C1864184","MEDGEN:350360","OMIM:603119"],"synonyms":[{"name":"apraxia of eyelid opening","type":"exact"}],"termid":"MONDO:0011289","xrefs":{"Monarch":{"xref_id":"0011289"}}}


id: PBO:0052313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA0825","termid":"PBO:0052313"}


id: PBO:0056897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial elongation factor 2","termid":"PBO:0056897"}


id: PBO:0109103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 41, pseudogene","termid":"PBO:0109103"}


id: GO:0110041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of nematode pharynx morphogenesis, the process in which the anatomical structure of the pharynx is generated and organized.","definition_xrefs":["GOC:rz","PMID:20805556"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of animal organ morphogenesis","termid":"GO:2000027"},{"relation_name":"regulates","term_name":"nematode pharynx morphogenesis","termid":"GO:0110040"}],"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 nematode pharynx morphogenesis","termid":"GO:0110041"}


id: PBO:0076350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SYT15 antisense RNA 1","termid":"PBO:0076350"}


id: PR:Q9P6Q1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A proline synthase co-transcribed bacterial homolog protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10146:SF0","PRO:DNx","OMA:SCHPO01126"],"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":"UPF0001 protein C644.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC644.09","secondary_identifiers":["UniProtKB:Q9P6Q1"],"synonyms":[{"name":"Spom972h-PROSC","type":"exact"}],"termid":"PR:Q9P6Q1"}


id: PBO:0059364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S18A pseudogene 1","termid":"PBO:0059364"}


id: PBO:0069110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 359, pseudogene","termid":"PBO:0069110"}


id: PBO:0065569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostaglandin I2 synthase","termid":"PBO:0065569"}


id: PBO:0057394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548f-2","termid":"PBO:0057394"}


id: GO:0015660
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of formate from the inside of the cell to the outside of the cell across a membrane.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formate transmembrane transporter activity","termid":"GO:0015499"},{"relation_name":"is_a","term_name":"efflux transmembrane transporter activity","termid":"GO:0015562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"formate efflux transmembrane transporter activity","secondary_identifiers":["GO:0015509"],"synonyms":[{"name":"formate efflux permease activity","type":"related"}],"termid":"GO:0015660"}


id: GO:0002238
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus by molecules of fungal origin such as chito-octamer oligosaccharide.","definition_xrefs":["GOC:rl","GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to external biotic stimulus","termid":"GO:0043207"},{"relation_name":"part_of","term_name":"response to fungus","termid":"GO:0009620"}],"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 molecule of fungal origin","synonyms":[{"name":"response to fungus associated molecule","type":"exact"}],"termid":"GO:0002238"}


id: PBO:0052795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 35","termid":"PBO:0052795"}


id: GO:1901754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of vitamin D3.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin D catabolic process","termid":"GO:0042369"},{"relation_name":"is_a","term_name":"alcohol catabolic process","termid":"GO:0046164"},{"relation_name":"is_a","term_name":"vitamin D3 metabolic process","termid":"GO:0070640"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0006766","GO:0008150"],"is_obsolete":false,"name":"vitamin D3 catabolic process","synonyms":[{"name":"calciol breakdown","type":"exact"},{"name":"calciol catabolic process","type":"exact"},{"name":"calciol catabolism","type":"exact"},{"name":"calciol degradation","type":"exact"},{"name":"cholecalciferol catabolic process","type":"exact"},{"name":"cholecalciferol catabolism","type":"exact"},{"name":"vitamin D3 breakdown","type":"exact"},{"name":"vitamin D3 catabolism","type":"exact"},{"name":"vitamin D3 degradation","type":"exact"}],"termid":"GO:1901754"}


id: PBO:0078613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 64D, pseudogene","termid":"PBO:0078613"}


id: MONDO:0002938
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A skin carcinoma displaying cytological characteristics intermediate to nodular basal cell carcinoma and squamous cell carcinoma.","definition_xrefs":["NCIT:C66903"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"metatypical basal cell carcinoma","secondary_identifiers":["DOID:4281","ICDO:8095/3","SCTID:254702000"],"synonyms":[{"name":"basosquamous carcinoma of skin","type":"exact"},{"name":"skin metatypical basal cell carcinoma","type":"exact"},{"name":"skin metatypical carcinoma","type":"exact"}],"termid":"MONDO:0002938","xrefs":{"Monarch":{"xref_id":"0002938"}}}


id: PBO:0072081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S12 pseudogene 11","termid":"PBO:0072081"}


id: MONDO:0011615
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"},{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"East Texas bleeding disorder","secondary_identifiers":["MEDGEN:342980","GARD:17613","OMIM:605913","UMLS:C1853831","MESH:C565275","Orphanet:391320"],"synonyms":[{"name":"Bdet","type":"related"},{"name":"bleeding disorder, EAST Texas type","type":"related"}],"termid":"MONDO:0011615","xrefs":{"Monarch":{"xref_id":"0011615"}}}


id: MONDO:0013855
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"influenza, severe, susceptibility to","secondary_identifiers":["MEDGEN:766376","OMIM:614680","UMLS:C3553462"],"synonyms":[{"name":"influenza, severe, susceptibility to","type":"exact"},{"name":"susceptibility to severe influenza","type":"related"}],"termid":"MONDO:0013855","xrefs":{"Monarch":{"xref_id":"0013855"}}}


id: PBO:0089777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate decarboxylase family protein","termid":"PBO:0089777"}


id: GO:1900993
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of (-)-secologanin.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00328","GOC:yaf"],"gene_count":0,"genotype_count":0,"name":"obsolete (-)-secologanin catabolic process (obsolete GO:1900993)","synonyms":[{"name":"(-)-secologanin breakdown","type":"exact"},{"name":"(-)-secologanin catabolism","type":"exact"},{"name":"(-)-secologanin degradation","type":"exact"}],"termid":"GO:1900993"}


id: PBO:0064821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 3C","termid":"PBO:0064821"}


id: PBO:0005811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin Sal3","termid":"PBO:0005811"}


id: GO:0020035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The adherence of symbiont-infected erythrocytes to microvascular endothelium via symbiont proteins embedded in the membrane of the erythrocyte.","definition_xrefs":["PMID:10362584","GOC:mb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adhesion of symbiont to host cell","termid":"GO:0044650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"adhesion of symbiont to microvasculature","secondary_identifiers":["GO:0043706"],"synonyms":[{"name":"cytoadherence to microvasculature, mediated by parasite protein","type":"narrow"},{"name":"cytoadherence to microvasculature, mediated by symbiont protein","type":"exact"},{"name":"heterophilic cell adhesion involved in cytoadherence to microvasculature, mediated by parasite protein","type":"narrow"},{"name":"parasite-protein-mediated cytoadherence to microvasculature","type":"narrow"},{"name":"symbiont-protein-mediated cytoadherence to microvasculature","type":"broad"}],"termid":"GO:0020035"}


id: PBO:0002734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1,3-beta-glucan synthase subunit Bgs3","termid":"PBO:0002734"}


id: PBO:0000183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP complex subunit Trs33 (predicted)","termid":"PBO:0000183"}


id: GO:1903296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of glutamate secretion, where glutamate acts as a neurotransmitter.","definition_xrefs":["GOC:TermGenie","PMID:16782817","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of neurotransmitter secretion","termid":"GO:0001956"},{"relation_name":"is_a","term_name":"positive regulation of glutamate secretion","termid":"GO:0014049"},{"relation_name":"is_a","term_name":"positive regulation of synaptic transmission, glutamatergic","termid":"GO:0051968"},{"relation_name":"is_a","term_name":"regulation of glutamate secretion, neurotransmission","termid":"GO:1903294"},{"relation_name":"positively_regulates","term_name":"glutamate secretion, neurotransmission","termid":"GO:0061535"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of glutamate secretion, neurotransmission","synonyms":[{"name":"activation of glutamate secretion, neurotransmission","type":"narrow"},{"name":"up regulation of glutamate secretion, neurotransmission","type":"exact"},{"name":"up-regulation of glutamate secretion, neurotransmission","type":"exact"},{"name":"upregulation of glutamate secretion, neurotransmission","type":"exact"}],"termid":"GO:1903296"}


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


id: GO:0033402
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a UUC codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0060090","GO:0003674","GO:0005488","GO:0003723"],"is_obsolete":false,"name":"UUC codon-amino acid adaptor activity","synonyms":[{"name":"TTC codon-amino acid adaptor activity","type":"exact"},{"name":"phenylalanine tRNA","type":"related"}],"termid":"GO:0033402"}


id: PBO:0087218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scaffold protein; assists in association of proteasome core particle with regulatory particle; inhibitor of proteasome in vivo and in vitro; inhibits proteasomal ATPase activity; degraded by the mature proteasome after assembly; contains HEAT-like repeats; protein increases in abundance and relocalizes from nucleus to cytoplasm upon DNA replication stress","termid":"PBO:0087218"}


id: PBO:0080156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"valosin containing protein","termid":"PBO:0080156"}


id: PBO:0071288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 11","termid":"PBO:0071288"}


id: PBO:0044181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"catenin delta 1","termid":"PBO:0044181"}


id: PR:Q09926
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pcr1 gene.","definition_xrefs":["UniProtKB:Q09926","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":"transcription factor pcr1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC21E11.03c","synonyms":[{"name":"Spom972h-pcr1","type":"exact"},{"name":"transcription factor mts2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09926"}


id: PBO:0065680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidyl-tRNA hydrolase 2","termid":"PBO:0065680"}


id: PBO:0089429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human WDR55 family, involved in ribosome biogenesis","termid":"PBO:0089429"}


id: GO:0050151
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-10-hydroxystearate = H2O + oleate.","definition_xrefs":["RHEA:21852","EC:4.2.1.53"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"oleate hydratase activity","secondary_identifiers":["KEGG_REACTION:R02813","MetaCyc:OLEATE-HYDRATASE-RXN"],"synonyms":[{"name":"(R)-10-hydroxystearate 10-hydro-lyase (oleate-forming)","type":"related"},{"name":"(R)-10-hydroxystearate 10-hydro-lyase activity","type":"related"}],"termid":"GO:0050151"}


id: PBO:0059735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 9","termid":"PBO:0059735"}


id: GO:0006352
data:
  {"annotated_genes":["SJAG_04274","SJAG_03206","SJAG_02494","SJAG_00349","SJAG_02600","SJAG_04977","SJAG_03944","SJAG_00116","SJAG_02541","SJAG_01016","SJAG_02391","SJAG_04758","SJAG_01475","SJAG_01230","SJAG_02813","SJAG_05192","SJAG_02747","SJAG_00758","SJAG_03095","SJAG_01808","SJAG_04647","SJAG_01110","SJAG_00202","SJAG_00087","SJAG_01622","SJAG_03884","SJAG_00584","SJAG_00766","SJAG_00995","SJAG_00441","SJAG_04097","SJAG_03599","SJAG_00045","SJAG_02066","SJAG_00119","SJAG_02458","SJAG_03285","SJAG_00769","SJAG_02773","SJAG_03758","SJAG_02815","SJAG_03421","SJAG_03787","SJAG_02254","SJAG_04852","SJAG_03752","SJAG_04576","SJAG_04099","SJAG_00741","SJAG_05331","SJAG_04614","SJAG_02872","SJAG_04205","SJAG_03900","SJAG_03145","SJAG_03618","SJAG_00735","SJAG_02174","SJAG_01611","SJAG_02906","SJAG_01403","SJAG_02768","SJAG_02571","SJAG_01465","SJAG_00873","SJAG_05339","SJAG_00297","SJAG_01562","SJAG_00421","SJAG_04894","SJAG_01207","SJAG_02927","SJAG_02549","SJAG_04755","SJAG_03255","SJAG_03366","SJAG_00540","SJAG_02303","SJAG_02869","SJAG_01711","SJAG_04038","SJAG_01804","SJAG_03576","SJAG_04989","SJAG_03120","SJAG_03431","SJAG_04596","SJAG_02846","SJAG_02981","SJAG_00896","SJAG_02329","SJAG_04030","SJAG_03035","SJAG_03956","SJAG_03776","SJAG_00650","SJAG_03573","SJAG_01523","SJAG_00159","SJAG_02500","SJAG_00184","SJAG_01952","SJAG_00581","SJAG_02170","SJAG_05020","SJAG_05203","SJAG_00872","SJAG_00095","SJAG_00585","SJAG_04213","SJAG_01710","SJAG_03579","SJAG_03107","SJAG_04194","SJAG_03839","SJAG_02385","SJAG_03694","SJAG_02691","SJAG_01713","SJAG_00067","SJAG_00868","SJAG_02101","SJAG_01653","SJAG_00342","SJAG_00634","SJAG_02551","SJAG_02849","SJAG_01744","SJAG_01765","SJAG_00458","SJAG_00512","SJAG_04917","SJAG_03590","SJAG_01827","SJAG_00150","SJAG_04368","SJAG_00739","SJAG_03668","SJAG_01658","SJAG_01771","SJAG_03014","SJAG_04820","SJAG_01436","SJAG_07011","SJAG_03033","SJAG_05313","SJAG_00440","SJAG_04420","SJAG_04613","SJAG_03211","SJAG_00641","SJAG_00746","SJAG_00904","SJAG_05341","SJAG_02798","SJAG_01712","SJAG_03441","SJAG_01513","SJAG_04654","SJAG_04705","SJAG_04766","SJAG_00901","SJAG_04005","SJAG_01325","SJAG_02447","SJAG_00909","SJAG_00743","SJAG_02466","SJAG_03007","SJAG_03289","SJAG_01111","SJAG_03622","SJAG_02589","SJAG_03354","SJAG_00692","SJAG_02314"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79898,90032],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045899"},{"annotations":[103735,95705,94773,99346,102276,103993,106563,106698,115064,115627,98997,91004,90691,106374,87768,119264,106021,94662,109073,96185,109046],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0060261"},{"annotations":[68837,64201,77856],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001188"},{"annotations":[70850,75276,71046,72279,75947,67581,77589,71694,94468,74028,77183,74824],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051123"},{"annotations":[72143,103389],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070898"},{"annotations":[87732,98499,95462],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006391"},{"annotations":[108004,71753,93501,110105,95900,110062,72674,79503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006361"},{"annotations":[92359,95901,94235,94420,97135,70470,103474,113297,114559,115472,108806,71205,80733,79482,73123,108209,105831,90214,76529,92498,67939,103934,105791,57537,79302,70662,112417,115160,100548,80655,108017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006367"},{"annotations":[107250,71466,56989,80142,88507,115696,95902,74110,89242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006384"},{"annotations":[94478,98559,112882,109793,113480,101298,114637,117944,107649,98824,105358,108198,97409,94534,95797,88663,94506,88121,115718,90915,115732,114728,99463,88479,93120,90391,94334,98990,104166,116616,107762,104888,107075,88302,91034,88813,91020,113306,118295,87973,116034,113461,117600,96208,108000,94104,115586,96215,90119,96771,99713,89605,105350,109390,112082,101882,114552,114563,115342,94458,107227,116677,117235,115050,91735,105950,113650,117874,110938,92619,106099,93839,103100,108786,116866,117896,95772,109669,117781,89433,110803,94444,96974,89198,98145,94966,94631,103439,103686,109901],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045815"},{"annotations":[77587],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001174"}]},"cv_name":"biological_process","definition":"The initial step of transcription, consisting of the assembly of the RNA polymerase preinitiation complex (PIC) at a gene promoter, as well as the formation of the first few bonds of the RNA transcript. 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id: GO:0034668
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An integrin complex that comprises one alpha4 subunit and one beta1 subunit.","definition_xrefs":["PMID:12297042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integrin complex","termid":"GO:0008305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"integrin alpha4-beta1 complex","synonyms":[{"name":"ITGA4-ITGB1 complex","type":"narrow"},{"name":"VLA-4 complex","type":"exact"},{"name":"alpha4-beta1 integrin complex","type":"exact"}],"termid":"GO:0034668"}


id: PBO:0081800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 729","termid":"PBO:0081800"}


id: SO:1000023
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Change of a purine nucleotide, A or G , into a pyrimidine nucleotide C or T.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transversion","termid":"SO:1000017"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purine_to_pyrimidine_transversion","synonyms":[{"name":"purine to pyrimidine transversion","type":"exact"}],"termid":"SO:1000023"}


id: PBO:0043005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chitinase, acidic pseudogene 3","termid":"PBO:0043005"}


id: PBO:0088229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, zf-fungal binuclear cluster type","termid":"PBO:0088229"}


id: PBO:0041694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caldesmon 1","termid":"PBO:0041694"}


id: PBO:0114381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane carboxylic acid transmembrane transporter","termid":"PBO:0114381"}


id: MONDO:0008841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ataxia telangiectasia","termid":"MONDO:0008840"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005047","MONDO:0005046","MONDO:0005559"],"is_obsolete":false,"name":"ataxia-telangiectasia with generalized skin pigmentation and early death","secondary_identifiers":["GARD:15141","OMIM:208910","MESH:C565930","UMLS:C1859615","MEDGEN:395306"],"synonyms":[{"name":"ataxia-telangiectasia with generalized skin pigmentation and early death","type":"exact"}],"termid":"MONDO:0008841","xrefs":{"Monarch":{"xref_id":"0008841"}}}


id: MONDO:0014239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"46,XY partial gonadal dysgenesis","termid":"MONDO:0016674"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testicular anomalies with or without congenital heart disease","secondary_identifiers":["UMLS:C3809858","GARD:18360","MEDGEN:816188","OMIM:615542"],"synonyms":[{"name":"TACHD","type":"related"},{"name":"testicular anomalies with or without congenital heart disease","type":"exact"}],"termid":"MONDO:0014239","xrefs":{"Monarch":{"xref_id":"0014239"}}}


id: PBO:0061003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NHS actin remodeling regulator","termid":"PBO:0061003"}


id: PBO:0043326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC like kinase 3","termid":"PBO:0043326"}


id: GO:0044489
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 activity of a voltage-gated sodium channel in another organism.","definition_xrefs":["GOC:jl","GOC:fj","PMID:21781281"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of voltage-gated sodium channel activity in another organism (obsolete GO:0044489)","synonyms":[{"name":"negative regulation of voltage-gated sodium channel activity in other organism","type":"exact"}],"termid":"GO:0044489"}


id: PBO:0113113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endocytic adaptor; K63-specific Ub-chain binding protein involved in receptor endocytosis; scaffold protein that localizes to nascent endocytic sites after homo-oligomerization and organizes the endocytic machinery; role in autophagy of aberrant clathrin-mediated endocytosis protein condensates; binds membranes in a Ub-dependent manner; interacts with and functions upstream of Cmk2p to suppress stress-induced non-apoptotic cell death; putative cytokinesis regulator;  homolog of mammalian Eps15","termid":"PBO:0113113"}


id: PBO:0086371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative aryl alcohol dehydrogenase; similar to Phanerochaete chrysosporium aryl alcohol dehydrogenase; ORFs AAD6/YFL056C and AAD16/YFL057C are displaced from one another by -1 frameshift; members of the AAD gene family comprise three pairs (AAD3 + AAD15, AAD6/AAD16 + AAD4, AAD10 + AAD14) whose two genes are more related to one another than to other members of the family","termid":"PBO:0086371"}


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


id: MONDO:0958179
data:
  {"annotated_genes":["SJAG_03861"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85337],"is_not":false,"summary":null,"term":"MONDO:0958179"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"glycine encephalopathy","termid":"MONDO:0011612"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03861":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"glycine encephalopathy 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:605899"],"termid":"MONDO:0958179","terms_by_termid":{"MONDO:0958179":null},"xrefs":{"Monarch":{"xref_id":"0958179"}}}


id: PBO:0000919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex subunit Apc8","termid":"PBO:0000919"}


id: PBO:0075209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide N","termid":"PBO:0075209"}


id: MONDO:0017603
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"ALK-negative anaplastic large cell lymphoma (ALK- ALCL) is a type of ALCL, a rare and aggressive peripheral T-cell non-Hodgkin lymphoma affecting lymph nodes and extranodal sites, which is characterized by the lack of expression of a protein called anaplastic lymphoma kinase (ALK).","definition_xrefs":["Orphanet:300903"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anaplastic large cell lymphoma","termid":"MONDO:0020325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"ALK-negative anaplastic large cell lymphoma","secondary_identifiers":["ICDO:9702/3","UMLS:C1332078","EFO:1000083","GARD:21252","MEDGEN:272266","NCIT:C37194"],"synonyms":[{"name":"ALCL, ALK-","type":"exact"},{"name":"ALK- ALCL","type":"exact"},{"name":"ALK- anaplastic large cell lymphoma","type":"exact"},{"name":"ALK-negative anaplastic large cell lymphoma","type":"exact"},{"name":"anaplastic large cell lymphoma, ALK-negative","type":"exact"}],"termid":"MONDO:0017603","xrefs":{"Monarch":{"xref_id":"0017603"}}}


id: MONDO:0010099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"GM2 gangliosidosis, AB variant is an extremely rare, severe genetic disorder characterized by progressive neurological decline due to ganglioside activator deficiency.","definition_xrefs":["Orphanet:309246"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GM2 gangliosidosis","termid":"MONDO:0017720"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002525","MONDO:0002561","MONDO:0005066"],"is_obsolete":false,"name":"Tay-Sachs disease AB variant","secondary_identifiers":["NANDO:2201201","NANDO:1200073","MEDGEN:78657","GARD:17406","NCIT:C133084","UMLS:C0268275","DOID:4795","MESH:D049290","SCTID:71253000","OMIM:272750"],"synonyms":[{"name":"Ab variant GM2-gangliosidosis","type":"related"},{"name":"GM2 activator deficiency","type":"related"},{"name":"GM2 gangliosidosis, AB variant","type":"related"},{"name":"GM2-gangliosidosis, AB variant","type":"related"},{"name":"Tay-Sachs disease, AB variant","type":"related"},{"name":"Tay-Sachs disease, variant AB","type":"exact"},{"name":"hexosaminidase activator deficiency","type":"exact"}],"termid":"MONDO:0010099","xrefs":{"Monarch":{"xref_id":"0010099"}}}


id: GO:0071452
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 singlet oxygen stimulus. Singlet oxygen is a dioxygen (O2) molecule in which two 2p electrons have similar spin. Singlet oxygen is more highly reactive than the form in which these electrons are of opposite spin, and it is produced in mutant chloroplasts lacking carotenoids and by leukocytes during metabolic burst.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to singlet oxygen","termid":"GO:0000304"},{"relation_name":"is_a","term_name":"cellular response to reactive oxygen species","termid":"GO:0034614"}],"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 singlet oxygen","termid":"GO:0071452"}


id: GO:1904593
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to prostaglandin.","definition_xrefs":["GO_REF:0000067","GOC:TermGenie","PMID:21445266"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid derivative binding","termid":"GO:1901567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008289"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0008289"],"is_obsolete":false,"name":"prostaglandin binding","termid":"GO:1904593"}


id: GO:0042354
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving L-fucose, 6-deoxy-L-galactose, a sugar that occurs in fucans, a class of polysaccharides in seaweeds, especially Fucus species, and in the cell wall matrix of higher plants.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fucose metabolic process","termid":"GO:0006004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"L-fucose metabolic process","synonyms":[{"name":"L-fucose metabolism","type":"exact"}],"termid":"GO:0042354"}


id: PBO:0034049
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-child_nucleus_of_in_male","termid":"PBO:0034049"}


id: FYPO:0000458
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 methylation of lysine at position 9 of histone H3 is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone methylation during vegetative growth","termid":"FYPO:0000457"},{"relation_name":"is_a","term_name":"abnormal histone H3-K9 methylation","termid":"FYPO:0007466"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0005447","FYPO:0001985","FYPO:0002494","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal histone H3-K9 methylation during vegetative growth","synonyms":[{"name":"abnormal histone H3 K9 methylation during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K9 methylation during mitotic cell cycle","type":"related"},{"name":"abnormal histone H3K9me during vegetative growth","type":"exact"},{"name":"abnormal histone lysine H3 K9 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000458"}


id: PBO:0051666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inner centromere protein","termid":"PBO:0051666"}


id: PBO:0052097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel modulatory factor 1","termid":"PBO:0052097"}


id: GO:0008821
data:
  {"annotated_genes":["SJAG_00623","SJAG_03675","SJAG_01044","SJAG_05237","SJAG_02708","SJAG_04752"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[59689,74754,78881,79510,95062,101497],"is_not":false,"summary":null,"term":"GO:0008821"}]},"cv_name":"molecular_function","definition":"Catalysis of the endonucleolytic cleavage at a junction such as a reciprocal single-stranded crossover between two homologous DNA duplexes (Holliday junction).","definition_xrefs":["EC:3.1.21.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA endonuclease activity, producing 3'-phosphomonoesters","termid":"GO:0016889"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00623":null,"SJAG_01044":null,"SJAG_02708":null,"SJAG_03675":null,"SJAG_04752":null,"SJAG_05237":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0140097","GO:0016788","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"crossover junction DNA endonuclease activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:3.1.22.4-RXN","GO:0008844"],"synonyms":[{"name":"Hje endonuclease activity","type":"related"},{"name":"Holliday junction endonuclease CCE1 activity","type":"narrow"},{"name":"Holliday junction nuclease activity","type":"related"},{"name":"Holliday junction resolvase activity","type":"narrow"},{"name":"RusA endonuclease activity","type":"narrow"},{"name":"RuvC endonuclease activity","type":"narrow"},{"name":"SpCCe1 Holliday junction resolvase activity","type":"narrow"},{"name":"SpCCe1 holliday junction resolvase","type":"narrow"},{"name":"crossover junction endodeoxyribonuclease activity","type":"exact"},{"name":"crossover junction endoribonuclease activity","type":"exact"},{"name":"cruciform-cutting endonuclease activity","type":"related"},{"name":"endo X3","type":"related"},{"name":"endodeoxyribonuclease RUS activity","type":"exact"},{"name":"endonuclease RuvC activity","type":"narrow"},{"name":"endonuclease VII activity","type":"narrow"},{"name":"endonuclease X3 activity","type":"narrow"}],"termid":"GO:0008821","terms_by_termid":{"GO:0008821":null}}


id: MONDO:1010952
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Embryonal rhabdomyosarcoma that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bovine neoplasm","termid":"MONDO:0700134"},{"relation_name":"is_a","term_name":"embryonal rhabdomyosarcoma, non-human animal","termid":"MONDO:1010216"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"embryonal rhabdomyosarcoma, cattle","secondary_identifiers":["OMIA:001921-9913"],"termid":"MONDO:1010952","xrefs":{"Monarch":{"xref_id":"1010952"}}}


id: PBO:0003736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sm snRNP core protein Smd3","termid":"PBO:0003736"}


id: PATO:0002437
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's being locked together or interconnected to another entity.","definition_xrefs":["merriam-webster:merriam-webster"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interlocked with","termid":"PATO:0002437"}


id: PR:Q9P7L8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sap62 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7L8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA-splicing factor sap62 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21C3.05","synonyms":[{"name":"Spom972h-sap62","type":"exact"},{"name":"spliceosome-associated protein 62 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7L8"}


id: PBO:0027736
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-protein_mislocalized_to_nucleolus_during_mitotic_telophase","termid":"PBO:0027736"}


id: PBO:0076721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trichohyalin like 1","termid":"PBO:0076721"}


id: PBO:0072811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterile alpha motif domain containing 7","termid":"PBO:0072811"}


id: MONDO:0017301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pericardial and diaphragmatic defect is a rare combination of absent pericardium with congenital diaphragmatic defect.","definition_xrefs":["Orphanet:2847"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pericardial and diaphragmatic defect","secondary_identifiers":["UMLS:C4510305","GARD:18780","MEDGEN:1373904"],"termid":"MONDO:0017301","xrefs":{"Monarch":{"xref_id":"0017301"}}}


id: PBO:0013766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-actin capping protein beta subunit Acp2","termid":"PBO:0013766"}


id: PBO:0089904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ThiJ domain protein, implicated in cellular detoxification","termid":"PBO:0089904"}


id: MONDO:0008151
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gnathodiaphyseal dysplasia (GDD) is a bone dysplasia characterized by bone fragility, frequent bone fractures at a young age, cemento-osseous lesions of the jaw bones, bowing of tubular bones (tibia and fibula) and diaphyseal sclerosis of long bones associated with generalized osteopenia. GD follows an autosomal dominant mode of transmission.","definition_xrefs":["Orphanet:53697"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"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":"gnathodiaphyseal dysplasia","secondary_identifiers":["icd11.foundation:1984860886","UMLS:C1833736","MEDGEN:331575","MESH:C536039","SCTID:715568002","DOID:0111533","OMIM:166260","GARD:8698"],"synonyms":[{"name":"GDD","type":"exact"},{"name":"GNATHODIAPHYSEAL dysplasia","type":"related"},{"name":"Gnathodiaphyseal sclerosis","type":"related"},{"name":"Levin syndrome 2","type":"related"},{"name":"gnathodiaphyseal dysplasia","type":"exact"},{"name":"osteogenesis imperfecta Levin type","type":"related"},{"name":"osteogenesis imperfecta with unusual skeletal lesions","type":"related"}],"termid":"MONDO:0008151","xrefs":{"Monarch":{"xref_id":"0008151"}}}


id: SO:0000636
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Snall nuclear RNAs that are incorporated into the pre-mRNAs to replace the 5' end in some eukaryotes.","definition_xrefs":["PMID:24130571"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary_transcript_region","termid":"SO:0000835"},{"relation_name":"part_of","term_name":"mini_exon_donor_RNA","termid":"SO:0000635"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spliced_leader_RNA","synonyms":[{"name":"mini-exon","type":"related"},{"name":"spliced leader RNA","type":"exact"}],"termid":"SO:0000636"}


id: SO:0001895
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature ablation whereby the deleted region includes a transcription factor binding site.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulatory_region_ablation","termid":"SO:0001894"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFBS_ablation","secondary_identifiers":["http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences"],"synonyms":[{"name":"TFBS ablation","type":"exact"},{"name":"VEP:TFBS_ablation","type":"exact"},{"name":"transcription factor binding site ablation","type":"exact"}],"termid":"SO:0001895"}


id: MONDO:1010856
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Krabbe disease that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Krabbe disease, non-human animal","termid":"MONDO:1010170"},{"relation_name":"is_a","term_name":"lysosomal storage disease, domestic cat","termid":"MONDO:1010861"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Krabbe disease, domestic cat","secondary_identifiers":["OMIA:000578-9685"],"termid":"MONDO:1010856","xrefs":{"Monarch":{"xref_id":"1010856"}}}


id: PBO:0074800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 13E","termid":"PBO:0074800"}


id: GO:0080033
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 nitrite stimulus.","definition_xrefs":["PMID:17951451","GOC:dhl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to nitrite","termid":"GO:0080033"}


id: GO:0051786
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: all-trans-13,14-dihydroretinol + A = all-trans-retinol + AH(2). Note that this reaction has only been observed to occur in the opposite direction.","definition_xrefs":["RHEA:19193","EC:1.3.99.23"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors","termid":"GO:0016627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"all-trans-retinol 13,14-reductase activity","secondary_identifiers":["KEGG_REACTION:R07163","Reactome:R-HSA-8956427","MetaCyc:1.3.99.23-RXN"],"synonyms":[{"name":"(13,14)-all-trans-retinol saturase activity","type":"exact"},{"name":"RetSat activity","type":"related"},{"name":"all-trans-13,14-dihydroretinol:acceptor 13,14-oxidoreductase activity","type":"exact"},{"name":"all-trans-retinol:all-trans-13,14-dihydroretinol saturase activity","type":"exact"},{"name":"retinol saturase activity","type":"related"}],"termid":"GO:0051786"}


id: PomGeneEx:0000006
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneEx","definition":"A gene expression qualifier that indicates that an RNA or protein is not detectable under a given set of conditions or at an indicated time.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene expression qualifier","termid":"PomGeneEx:0000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"absent","synonyms":[{"name":"gene expression absent","type":"exact"},{"name":"gene product absent","type":"exact"}],"termid":"PomGeneEx:0000006"}


id: GO:0061562
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to creating the structural organization of a cranial ganglion. This process pertains to the physical shaping of a rudimentary structure.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ganglion structural organization","termid":"GO:0061555"},{"relation_name":"part_of","term_name":"cranial nerve structural organization","termid":"GO:0021604"},{"relation_name":"part_of","term_name":"cranial ganglion morphogenesis","termid":"GO:0061559"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cranial ganglion structural organization","synonyms":[{"name":"cranial ganglia structural organization","type":"related"}],"termid":"GO:0061562"}


id: GO:0100006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that positively regulates sulfite transport.","definition_xrefs":["GOC:obol","GOC:cjm"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of sulfite transport by transcription from RNA polymerase II promoter (obsolete GO:0100006)","termid":"GO:0100006"}


id: GO:0120042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of macrophage proliferation.","definition_xrefs":["GOC:rph","GOC:BHF","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte proliferation","termid":"GO:0070664"},{"relation_name":"is_a","term_name":"regulation of macrophage proliferation","termid":"GO:0120040"},{"relation_name":"negatively_regulates","term_name":"macrophage proliferation","termid":"GO:0061517"}],"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 macrophage proliferation","termid":"GO:0120042"}


id: PBO:0086824
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; YNL033W has a paralog, YNL019C, that arose from a segmental duplication","termid":"PBO:0086824"}


id: SO:0002028
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An open reading frame that encodes a peptide of less than 100 amino acids.","definition_xrefs":["PMID:24705786","POMBASE:mah","PMID:23970561"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ORF","termid":"SO:0000236"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sORF","synonyms":[{"name":"smORF","type":"exact"},{"name":"small ORF","type":"exact"}],"termid":"SO:0002028"}


id: PBO:0081850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 783","termid":"PBO:0081850"}


id: GO:0052710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of N-alpha,N-alpha,N-alpha-trimethyl-L-histidine, also known as histidine betaine or hercynine, a trimethylated derivative of histidine.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid betaine catabolic process","termid":"GO:0006579"},{"relation_name":"is_a","term_name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolic process","termid":"GO:0052708"},{"relation_name":"is_a","term_name":"L-amino acid catabolic process","termid":"GO:0170035"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid catabolic process","termid":"GO:0170044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine catabolic process","synonyms":[{"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine breakdown","type":"exact"},{"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine catabolism","type":"exact"},{"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine degradation","type":"exact"},{"name":"hercynine breakdown","type":"exact"},{"name":"hercynine catabolic process","type":"exact"},{"name":"hercynine catabolism","type":"exact"},{"name":"hercynine degradation","type":"exact"},{"name":"histidine betaine breakdown","type":"exact"},{"name":"histidine betaine catabolic process","type":"exact"},{"name":"histidine betaine catabolism","type":"exact"},{"name":"histidine betaine degradation","type":"exact"}],"termid":"GO:0052710"}


id: FYPO:0001324
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell is lower than normal when the cell is in the vegetative growth phase of the life cycle. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level","termid":"FYPO:0000835"},{"relation_name":"is_a","term_name":"altered protein level during vegetative growth","termid":"FYPO:0001325"},{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0006551","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein level during vegetative growth","synonyms":[{"name":"decreased protein accumulation during vegetative growth","type":"related"},{"name":"decreased protein level during mitotic cell cycle","type":"related"},{"name":"reduced protein level during vegetative growth","type":"exact"}],"termid":"FYPO:0001324"}


id: PBO:0040760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beclin 1","termid":"PBO:0040760"}


id: GO:0044178
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding any of the compartments of the host cell Golgi apparatus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell membrane","termid":"GO:0033644"},{"relation_name":"part_of","term_name":"host cell endomembrane system","termid":"GO:0033645"},{"relation_name":"part_of","term_name":"host cell Golgi apparatus","termid":"GO:0044177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell Golgi membrane","synonyms":[{"name":"host Golgi membrane","type":"exact"}],"termid":"GO:0044178"}


id: GO:1905694
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of phosphatidic acid biosynthetic process.","definition_xrefs":["GO_REF:0000058","GOC:PARL","GOC:TermGenie","PMID:23767959","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of phospholipid biosynthetic process","termid":"GO:0071072"},{"relation_name":"is_a","term_name":"regulation of phosphatidic acid biosynthetic process","termid":"GO:1905693"},{"relation_name":"negatively_regulates","term_name":"phosphatidic acid biosynthetic process","termid":"GO:0006654"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of phosphatidic acid biosynthetic process","synonyms":[{"name":"down regulation of phosphatidic acid anabolism","type":"exact"},{"name":"down regulation of phosphatidic acid biosynthesis","type":"exact"},{"name":"down regulation of phosphatidic acid biosynthetic process","type":"exact"},{"name":"down regulation of phosphatidic acid formation","type":"exact"},{"name":"down regulation of phosphatidic acid synthesis","type":"exact"},{"name":"down-regulation of phosphatidic acid anabolism","type":"exact"},{"name":"down-regulation of phosphatidic acid biosynthesis","type":"exact"},{"name":"down-regulation of phosphatidic acid biosynthetic process","type":"exact"},{"name":"down-regulation of phosphatidic acid formation","type":"exact"},{"name":"down-regulation of phosphatidic acid synthesis","type":"exact"},{"name":"downregulation of phosphatidic acid anabolism","type":"exact"},{"name":"downregulation of phosphatidic acid biosynthesis","type":"exact"},{"name":"downregulation of phosphatidic acid biosynthetic process","type":"exact"},{"name":"downregulation of phosphatidic acid formation","type":"exact"},{"name":"downregulation of phosphatidic acid synthesis","type":"exact"},{"name":"inhibition of phosphatidic acid anabolism","type":"narrow"},{"name":"inhibition of phosphatidic acid biosynthesis","type":"narrow"},{"name":"inhibition of phosphatidic acid biosynthetic process","type":"narrow"},{"name":"inhibition of phosphatidic acid formation","type":"narrow"},{"name":"inhibition of phosphatidic acid synthesis","type":"narrow"},{"name":"negative regulation of phosphatidic acid anabolism","type":"exact"},{"name":"negative regulation of phosphatidic acid biosynthesis","type":"exact"},{"name":"negative regulation of phosphatidic acid formation","type":"exact"},{"name":"negative regulation of phosphatidic acid synthesis","type":"exact"}],"termid":"GO:1905694"}


id: GO:0042057
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binds to transforming growth factor beta receptor and anchors it to a particular subcellular location.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor anchoring activity (obsolete GO:0042057)","synonyms":[{"name":"TGF-beta receptor anchoring activity","type":"exact"},{"name":"TGFbeta receptor anchoring activity","type":"exact"},{"name":"transforming growth factor beta receptor anchor activity","type":"exact"},{"name":"transforming growth factor beta receptor anchoring activity","type":"exact"}],"termid":"GO:0042057"}


id: PBO:0056981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 30a","termid":"PBO:0056981"}


id: RO:0002134
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Relation between a 'neuron projection bundle' and a region in which one or more of its component neuron projections either synapses to targets or receives synaptic input.\\nT innervates some R\\nExpands_to: T has_fasciculating_neuron_projection that synapse_in some R.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"innervates","termid":"RO:0002134"}


id: FYPO:0005665
data:
  {"alleles_by_uniquename":{"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_04280:allele-1":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-1"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"},"SJAG_04703:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04703","name":"for3delta","uniquename":"SJAG_04703:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001369"}],"single_locus_phenotype":[{"annotations":[119546],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003315"},{"annotations":[119802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002026"},{"annotations":[119519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001369"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the amount, distribution, or morphology of all or part of the actin cytoskeleton is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cytoskeleton","termid":"FYPO:0002397"},{"relation_name":"output_of","term_name":"abnormal actin cytoskeleton organization","termid":"FYPO:0004803"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02392":null,"SJAG_04280":null,"SJAG_04522":null,"SJAG_04703":null},"genotype_count":4,"genotypes_by_uniquename":{"for3delta":{"display_name":"for3delta","display_uniquename":"for3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04703:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0004803","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04522","SJAG_04280"],"name":"abnormal actin cytoskeleton","references_by_uniquename":{"PMID:25866389":null,"PMID:30664646":null,"PMID:30726171":null},"single_locus_annotated_genes":["SJAG_02392","SJAG_04522","SJAG_04703"],"single_locus_genotype_uniquenames":["for3delta","rga4delta","pom1delta"],"synonyms":[{"name":"abnormal actin cytoskeleton physical object quality","type":"exact"}],"termid":"FYPO:0005665","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000338":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO:0003315":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PBO:0069986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1281, pseudogene","termid":"PBO:0069986"}


id: PBO:0051863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster assembly enzyme","termid":"PBO:0051863"}


id: GO:0034581
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-methyloct-2-enoyl-CoA + H2O = 3-hydroxy-4-methyloctanoyl-CoA.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 4-methyloct-2-enoyl-CoA hydratase activity (obsolete GO:0034581)","termid":"GO:0034581"}


id: MONDO:0005510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Collection of urine in the renal pelvis that results in dilatation of the renal pelvis and calyces. It is caused by obstruction of urine flow, nephrolithiasis, or vesicoureteral reflux. Signs and symptoms include flank pain, nausea, vomiting, fever, and dysuria.","definition_xrefs":["EFO:0005562"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary tract obstruction","termid":"MONDO:0003330"},{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"hydronephrosis","secondary_identifiers":["DOID:11111","NCIT:C26796","MEDGEN:42531","ICD9:591","SCTID:43064006","UMLS:C0020295","MESH:D006869"],"termid":"MONDO:0005510","xrefs":{"Monarch":{"xref_id":"0005510"}}}


id: PBO:0057439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 556","termid":"PBO:0057439"}


id: PR:O74477
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pca1 gene.","definition_xrefs":["UniProtKB:O74477","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":"metacaspase-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1840.04","synonyms":[{"name":"Spom972h-pca1","type":"exact"}],"termid":"PR:O74477"}


id: FYPO:0001173
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 hypermethylation of the 7-(mono)methylguanosine (m(7)G) cap structure at the 2' position of the guanosine residue to form a 2,2,7-trimethylguanosine cap structure is abolished.","definition_xrefs":["PomBase:mah","GO:0036261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished RNA modification","termid":"FYPO:0000371"},{"relation_name":"is_a","term_name":"abnormal 7-methylguanosine cap hypermethylation","termid":"FYPO:0001172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0006551","FYPO:0001985","FYPO:0000294","FYPO:0005447"],"is_obsolete":false,"name":"abolished 7-methylguanosine cap hypermethylation","synonyms":[{"name":"2,2,7-trimethylguanosine cap formation abolished","type":"exact"},{"name":"7-methylguanosine cap hypermethylation abolished","type":"exact"},{"name":"7-methylguanosine cap hypermethylation abolished during vegetative growth","type":"exact"},{"name":"TMG cap formation abolished","type":"exact"},{"name":"abolished 7-methylguanosine cap hypermethylation during mitotic cell cycle","type":"related"},{"name":"conversion of m(7)G to m(3)G abolished","type":"exact"},{"name":"snRNA capping abolished","type":"narrow"},{"name":"snoRNA capping abolished","type":"narrow"}],"termid":"FYPO:0001173"}


id: GO:1905128
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of axo-dendritic protein transport.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:20694152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of intracellular protein transport","termid":"GO:0090316"},{"relation_name":"is_a","term_name":"regulation of axo-dendritic protein transport","termid":"GO:1905126"},{"relation_name":"positively_regulates","term_name":"axo-dendritic protein transport","termid":"GO:0099640"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of axo-dendritic protein transport","synonyms":[{"name":"activation of axo-dendritic protein transport","type":"narrow"},{"name":"activation of axonal protein transport","type":"narrow"},{"name":"positive regulation of axonal protein transport","type":"narrow"},{"name":"up regulation of axo-dendritic protein transport","type":"exact"},{"name":"up regulation of axonal protein transport","type":"narrow"},{"name":"up-regulation of axo-dendritic protein transport","type":"exact"},{"name":"up-regulation of axonal protein transport","type":"narrow"},{"name":"upregulation of axo-dendritic protein transport","type":"exact"},{"name":"upregulation of axonal protein transport","type":"narrow"}],"termid":"GO:1905128"}


id: MONDO:0001999
data:
  {"annotated_genes":["SJAG_04757","SJAG_03866"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86960,86959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009935"}]},"cv_name":"mondo","definition":"Increased blood pressure in the arteries of the lungs; the etiology is unknown.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic pulmonary heart disease","termid":"MONDO:0001493"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03866":null,"SJAG_04757":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"primary pulmonary hypertension","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:14557","UMLS:C0152171","MEDGEN:57749","ICD10CM:I27.0","ICD9:416.0"],"synonyms":[{"name":"primary pulmonary hypertension","type":"exact"},{"name":"pulmonary hypertension, primary","type":"exact"}],"termid":"MONDO:0001999","terms_by_termid":{"MONDO:0009935":null},"xrefs":{"Monarch":{"xref_id":"0001999"}}}


id: GO:0009847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The physiological and developmental changes that occur in a spore following release from dormancy up to the earliest signs of growth (e.g. emergence from a spore wall).","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"}],"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":"spore germination","secondary_identifiers":["GO:0075005"],"synonyms":[{"name":"spore germination on or near host","type":"narrow"}],"termid":"GO:0009847"}


id: GO:0090317
data:
  {"annotated_genes":["SJAG_01311"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042308"}]},"cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the directed movement of proteins within cells.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of intracellular transport","termid":"GO:0032387"},{"relation_name":"is_a","term_name":"regulation of intracellular protein transport","termid":"GO:0033157"},{"relation_name":"is_a","term_name":"negative regulation of protein transport","termid":"GO:0051224"},{"relation_name":"negatively_regulates","term_name":"intracellular protein transport","termid":"GO:0006886"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01311":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of intracellular protein transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0090317","terms_by_termid":{"GO:0042308":null}}


id: MONDO:0003652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis in which the composition of the stones is predominantly urate.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephrolithiasis","termid":"MONDO:0008171"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"acute urate nephropathy","secondary_identifiers":["UMLS:C0341712","DOID:580","MEDGEN:574593","ICD9:583.9","NCIT:C123037","ICD9:274.11","SCTID:236496000","icd11.foundation:1011901523"],"synonyms":[{"name":"uric acid nephrolithiasis","type":"exact"},{"name":"uric acid urolithiasis","type":"exact"}],"termid":"MONDO:0003652","xrefs":{"Monarch":{"xref_id":"0003652"}}}


id: MONDO:0014662
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hereditary sensory neuropathy characterized by congenital insensitivity to pain and decreased sweating and tear production that has material basis in homozygous mutation in the PRDM12 gene on chromosome 9q34.","definition_xrefs":["DOID:0070153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"hereditary sensory and autonomic neuropathy","termid":"MONDO:0015364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0002320"],"is_obsolete":false,"name":"congenital insensitivity to pain-hypohidrosis syndrome","secondary_identifiers":["GARD:17866","OMIM:616488","Orphanet:478664","UMLS:C4225308","MEDGEN:894363"],"synonyms":[{"name":"CIP-hypohidrosis syndrome","type":"exact"},{"name":"HSAN 8","type":"related"},{"name":"HSAN8","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type 8","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type VIII","type":"exact"},{"name":"neuropathy, hereditary sensory and autonomic, type 8","type":"related"},{"name":"neuropathy, hereditary sensory and autonomic, type VIII","type":"related"}],"termid":"MONDO:0014662","xrefs":{"Monarch":{"xref_id":"0014662"}}}


id: GO:0018848
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: pinocarveol = carveol.","definition_xrefs":["UM-BBD_reactionID:r0715"],"gene_count":0,"genotype_count":0,"name":"obsolete pinocarveol isomerase activity (obsolete GO:0018848)","termid":"GO:0018848"}


id: MONDO:0011732
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial digital arthropathy-brachydactyly is characterized by the association of arthropathy of interphalangeal, metacarpophalangeal and metatarsophalangeal joints with brachydactyly of the middle and distal phalanges. It has been described in numerous members from five generations of one large family. Inheritance is autosomal dominant.","definition_xrefs":["Orphanet:85169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TRPV4-related bone disorder","termid":"MONDO:0018240"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial digital arthropathy-brachydactyly","secondary_identifiers":["MESH:C564656","NCIT:C175208","GARD:16735","MEDGEN:335678","UMLS:C1847406","OMIM:606835"],"synonyms":[{"name":"FDAB","type":"related"},{"name":"digital arthropathy-brachydactyly, familial","type":"related"}],"termid":"MONDO:0011732","xrefs":{"Monarch":{"xref_id":"0011732"}}}


id: PBO:0045849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 39","termid":"PBO:0045849"}


id: GO:0106200
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the translocation of amino acids and peptides linked to the hydrolysis of a nucleoside triphosphate.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete translocase activity acting on amio acids and peptides linked to the hydrolysis of a nucleoside triphosphate (obsolete GO:0106200)","termid":"GO:0106200"}


id: GO:0052521
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates, maintains or increases the frequency, rate or extent of phagocytosis, the engulfing by phagocytes of external particulate material, in the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by host of symbiont phagocytosis (obsolete GO:0052521)","synonyms":[{"name":"activation by host of symbiont phagocytosis","type":"narrow"},{"name":"stimulation by host of symbiont phagocytosis","type":"narrow"},{"name":"up regulation by host of symbiont phagocytosis","type":"exact"},{"name":"up-regulation by host of symbiont phagocytosis","type":"exact"},{"name":"upregulation by host of symbiont phagocytosis","type":"exact"}],"termid":"GO:0052521"}


id: PBO:0054316
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 1708","termid":"PBO:0054316"}


id: MONDO:0007651
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"gastrocutaneous syndrome","secondary_identifiers":["MEDGEN:338154","MESH:C535651","OMIM:137270","icd11.foundation:1431211717","Orphanet:2069","UMLS:C1850899","GARD:2438"],"synonyms":[{"name":"gastrocutaneous syndrome","type":"exact"},{"name":"peptic Ulcer/hiatal hernia, multiple lentigines/cafe-Au-lait Spots, hypertelorism, myopia","type":"related"}],"termid":"MONDO:0007651","xrefs":{"Monarch":{"xref_id":"0007651"}}}


id: GO:0002780
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an antibacterial peptide.","definition_xrefs":["PMID:11807545","GOC:add","ISBN:0781735149","PMID:15638771"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antimicrobial peptide biosynthetic process","termid":"GO:0002777"},{"relation_name":"part_of","term_name":"antibacterial peptide production","termid":"GO:0002778"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"antibacterial peptide biosynthetic process","termid":"GO:0002780"}


id: GO:0019596
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of mandelate, the anion of mandelic acid. Mandelic acid (alpha-hydroxybenzeneacetic acid) is an 8-carbon alpha-hydroxy acid (AHA) that is used in organic chemistry and as a urinary antiseptic.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mandelate metabolic process","termid":"GO:0018924"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"mandelate catabolic process","synonyms":[{"name":"mandelate breakdown","type":"exact"},{"name":"mandelate catabolism","type":"exact"},{"name":"mandelate degradation","type":"exact"}],"termid":"GO:0019596"}


id: PBO:0073234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO specific peptidase 7","termid":"PBO:0073234"}


id: PBO:0054494
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 1894","termid":"PBO:0054494"}


id: MONDO:0016272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A transitional cell carcinoma that involves the body of uterus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine carcinoma","termid":"MONDO:0005213"},{"relation_name":"is_a","term_name":"uterine corpus cancer","termid":"MONDO:0006003"},{"relation_name":"is_a","term_name":"transitional cell carcinoma","termid":"MONDO:0006474"}],"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":"transitional cell carcinoma of the corpus uteri","secondary_identifiers":["Orphanet:213746","MEDGEN:1676303","UMLS:C5191668","GARD:20484"],"synonyms":[{"name":"body of uterus transitional cell carcinoma","type":"exact"},{"name":"endometrial transitional cell carcinoma","type":"related"}],"termid":"MONDO:0016272","xrefs":{"Monarch":{"xref_id":"0016272"}}}


id: FYPO:0002556
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 of a cell is decreased, and the protein is instead detected distributed throughout the cell cortex of half of the cell nearer the non-growing end. There may be little or no protein detected at the medial cortex.","definition_xrefs":["PomBase:vw","PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to medial cortex, with protein distributed in cell cortex, during vegetative growth","termid":"FYPO:0006638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to medial cortex, with protein distributed in cell cortex near non-growing end, during vegetative growth","synonyms":[{"name":"abolished protein localization to medial cortex during vegetative growth, with protein distributed in cortex of non-growing half of cell","type":"narrow"},{"name":"decreased protein localisation to medial cortex during vegetative growth, with protein distributed in cell cortex near non-growing end","type":"exact"},{"name":"decreased protein localization to medial cortex during vegetative growth, with protein distributed in cell cortex near non-growing end","type":"exact"},{"name":"decreased protein localization to medial cortex during vegetative growth, with protein distributed in cell cortex near non-growing end, during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to medial cortex during vegetative growth, with protein distributed in cortex of non-growing half of cell","type":"exact"},{"name":"decreased protein localization to medial ring, with protein distributed in cell cortex near non-growing end, during vegetative growth","type":"exact"},{"name":"reduced protein localization to medial cortex during vegetative growth, with protein distributed in cell cortex near non-growing end","type":"exact"}],"termid":"FYPO:0002556"}


id: PR:O74764
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-dependent RNA helicase DDX55 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03226","PANTHER:PTHR24031:SF26","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":"ATP-dependent rRNA helicase spb4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC24C6.02","secondary_identifiers":["UniProtKB:O74764"],"synonyms":[{"name":"Spom972h-DDX55","type":"exact"}],"termid":"PR:O74764"}


id: FYPO:0001322
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_00426:allele-1":{"allele_type":"amino_acid_mutation","description":"P363S","gene_uniquename":"SJAG_00426","name":"bbl1-P363S","uniquename":"SJAG_00426:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"},"SJAG_01834:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01834","name":"pom152delta","uniquename":"SJAG_01834:allele-1"},"SJAG_01906:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01906","name":"nem1delta","uniquename":"SJAG_01906:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02763:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02763","name":"ned1delta","uniquename":"SJAG_02763:allele-1"},"SJAG_02763:allele-2":{"allele_type":"amino_acid_mutation","description":"D422E,D424E","gene_uniquename":"SJAG_02763","name":"ned1cat","synonyms":[{"name":"Catalytic 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physical cellular phenotype in which the amount, distribution, morphology, or other physical characteristic of a cell part is abnormal in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative 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subcellular component during mitotic cell cycle","type":"related"},{"name":"abnormal subcellular structure during vegetative growth","type":"related"}],"termid":"FYPO:0001322","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000338":null,"FYPO:0000118":null,"FYPO:0000356":null,"FYPO:0001369":null,"FYPO:0001556":null,"FYPO:0001784":null,"FYPO:0002026":null,"FYPO:0003315":null,"FYPO:0003727":null,"FYPO:0003779":null,"FYPO:0003976":null,"FYPO:0004890":null,"FYPO:0006433":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: MONDO:0011867
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microphthalmia with cyst, bilateral facial clefts, and limb anomalies","secondary_identifiers":["MEDGEN:375210","UMLS:C1843492","OMIM:607597","MESH:C564370"],"synonyms":[{"name":"microphthalmia with cyst, bilateral facial clefts, and limb anomalies","type":"exact"}],"termid":"MONDO:0011867","xrefs":{"Monarch":{"xref_id":"0011867"}}}


id: GO:0032145
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to succinate-semialdehyde dehydrogenase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"succinate-semialdehyde dehydrogenase binding","synonyms":[{"name":"succinic semialdehyde dehydrogenase binding","type":"exact"}],"termid":"GO:0032145"}


id: PBO:0034110
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-existence_starts_at_point","termid":"PBO:0034110"}


id: MONDO:0008275
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary osteolysis","termid":"MONDO:0019707"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial expansile osteolysis","secondary_identifiers":["MESH:C536335","MEDGEN:96593","DOID:0111542","Orphanet:85195","icd11.foundation:1161028858","GARD:9168","OMIM:174810","ICD9:756.9","UMLS:C0432292","SCTID:254153009"],"synonyms":[{"name":"EOF","type":"related"},{"name":"FEO","type":"related"},{"name":"HEPOD","type":"related"},{"name":"McCabe disease","type":"exact"},{"name":"Mccabe disease","type":"related"},{"name":"expansile osteolysis, familial","type":"related"},{"name":"familial expansile osteolysis","type":"exact"},{"name":"hereditary expansile polyostotic osteolytic dysplasia","type":"exact"},{"name":"osteolysis, familial expansile","type":"related"},{"name":"polyostotic osteolytic dysplasia, hereditary expansile","type":"related"}],"termid":"MONDO:0008275","xrefs":{"Monarch":{"xref_id":"0008275"}}}


id: PBO:0064247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLD5 pseudogene 1","termid":"PBO:0064247"}


id: FYPO:0001004
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which cells to resume growth normally upon exiting G0 phase.","definition_xrefs":["PMID:19366728","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable cell","termid":"FYPO:0000124"},{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"viable upon G0 to G1 transition","termid":"FYPO:0001004"}


id: PBO:0029498
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_curved_elongated_vegetative_cell_population_(obsolete_FYPO:0002217)","termid":"PBO:0029498"}


id: PBO:0079640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2Q2 pseudogene 11","termid":"PBO:0079640"}


id: SO:0001369
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"5_carboxymethylaminomethyluridine is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_carboxymethylaminomethyluridine","secondary_identifiers":["RNAMOD:077"],"synonyms":[{"name":"5-carboxymethylaminomethyluridine","type":"exact"},{"name":"cmnm5U","type":"exact"},{"name":"five carboxymethylaminomethyluridine","type":"exact"}],"termid":"SO:0001369"}


id: MONDO:0012124
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sudden infant death with dysgenesis of the testes (SIDDT) syndrome is a lethal condition in infants with dysgenesis of testes.","definition_xrefs":["Orphanet:168593"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sudden infant death-dysgenesis of the testes syndrome","secondary_identifiers":["MEDGEN:332428","MESH:C563856","GARD:12382","OMIM:608800","UMLS:C1837371"],"synonyms":[{"name":"SIDDT","type":"exact"},{"name":"sudden infant death - dysgenesis of the testes","type":"related"},{"name":"sudden infant death with dysgenesis of the testes syndrome","type":"related"}],"termid":"MONDO:0012124","xrefs":{"Monarch":{"xref_id":"0012124"}}}


id: GO:1990906
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cilium-like cell projection emanating from the inner segment and running alongside the outer segment of photoreceptors.","definition_xrefs":["PMID:25125189","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection","termid":"GO:0043005"}],"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":"accessory outer segment","termid":"GO:1990906"}


id: PBO:0040823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bridging integrator 2 pseudogene 1","termid":"PBO:0040823"}


id: PBO:0057805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3127","termid":"PBO:0057805"}


id: PBO:0003855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial manganese ion transporter (predicted)","termid":"PBO:0003855"}


id: PBO:0042108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 181","termid":"PBO:0042108"}


id: PBO:0039171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"A-kinase anchoring protein 3","termid":"PBO:0039171"}


id: PBO:0029496
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_chromosome_disjunction_at_meiosis_I","termid":"PBO:0029496"}


id: GO:1902012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of poly(ribitol phosphate) teichoic acid.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00790","PMID:11882717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teichoic acid biosynthetic process","termid":"GO:0019350"},{"relation_name":"is_a","term_name":"poly(ribitol phosphate) teichoic acid metabolic process","termid":"GO:1902011"}],"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":"part_of","termid":"GO:0071554"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044281","GO:0044085","GO:0071554","GO:0008150"],"is_obsolete":false,"name":"poly(ribitol phosphate) teichoic acid biosynthetic process","synonyms":[{"name":"poly(ribitol phosphate) teichoic acid anabolism","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid biosynthesis","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid formation","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid synthesis","type":"exact"}],"termid":"GO:1902012"}


id: PBO:0034553
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transcription_from_CRE_promoter","termid":"PBO:0034553"}


id: PBO:0062814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxysterol binding protein like 9 pseudogene 5","termid":"PBO:0062814"}


id: MOD:00495
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label","definition_xrefs":["Unimod:124#C","PubMed:12185208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"isotope tagged reagent derivatized residue","termid":"MOD:01426"}],"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":"N-iodoacetyl, p-chlorobenzyl-13C6-glucamine","synonyms":[{"name":"ICAT-H:13C(6)","type":"related"},{"name":"N-iodoacetyl, p-chlorobenzyl-13C6-glucamine","type":"related"}],"termid":"MOD:00495"}


id: MONDO:0008529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T-cell Subgroups, non-HLA-linked","secondary_identifiers":["OMIM:186950","MEDGEN:348312","UMLS:C1861277"],"synonyms":[{"name":"T-cell Subgroups, non-HLA-linked","type":"exact"}],"termid":"MONDO:0008529","xrefs":{"Monarch":{"xref_id":"0008529"}}}


id: GO:0016434
data:
  {"annotated_genes":["SJAG_03877","SJAG_02417"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95942,79286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009383"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + rRNA = S-adenosyl-L-homocysteine + rRNA containing methylcytosine.","definition_xrefs":["GOC:go-curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA methyltransferase activity","termid":"GO:0008649"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02417":null,"SJAG_03877":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:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0016741","GO:0140098","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"rRNA (cytosine) methyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0016434","terms_by_termid":{"GO:0009383":null}}


id: PBO:0039059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 8","termid":"PBO:0039059"}


id: MONDO:0011897
data:
  {"annotated_genes":["SJAG_00637","SJAG_04934"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86503,86504],"is_not":false,"summary":null,"term":"MONDO:0011897"}]},"cv_name":"mondo","definition":"A syndrome is characterized by ataxia, delayed dentition, hypomyelination and cerebral atrophy. So far, eight cases have been described.","definition_xrefs":["Orphanet:137639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"POLR3A-related disorder","termid":"MONDO:0700276"},{"relation_name":"is_a","term_name":"POLR3-related leukodystrophy","termid":"MONDO:0700282"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00637":null,"SJAG_04934":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060794","UMLS:C4706676","GARD:16948","SCTID:721846006","NANDO:2201297","MEDGEN:1639554","OMIM:607694","NANDO:1200585"],"synonyms":[{"name":"4H syndrome","type":"related"},{"name":"HLD7","type":"exact"},{"name":"ataxia, delayed dentition, and hypomyelination","type":"related"},{"name":"ataxia-delayed dentition-hypomyelination syndrome","type":"exact"},{"name":"ataxia-delayed dentition-hypomyelination syndrome; odontoleukodystrophy","type":"exact"},{"name":"dentoleukoencephalopathy","type":"related"},{"name":"hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism","type":"related"},{"name":"hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome","type":"related"},{"name":"hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome","type":"related"},{"name":"leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism","type":"related"},{"name":"leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism","type":"related"},{"name":"leukoencephalopathy, hypomyelinating, with ataxia and delayed dentition","type":"related"},{"name":"leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome","type":"exact"}],"termid":"MONDO:0011897","terms_by_termid":{"MONDO:0011897":null},"xrefs":{"Monarch":{"xref_id":"0011897"}}}


id: GO:0048625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a myoblast. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["GOC:dph","GOC:mtg_muscle","CL:0000056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate commitment","termid":"GO:0045165"},{"relation_name":"part_of","term_name":"myoblast differentiation","termid":"GO:0045445"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"myoblast fate commitment","termid":"GO:0048625"}


id: GO:0097207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A dormancy process in which dormancy (sometimes called a dormant state) is induced, maintained or broken in a bud. Bud dormancy is a suspension of most physiological activity and growth that can be reactivated. It may be a response to environmental conditions such as seasonality or extreme heat, drought, or cold. The exit from bud dormancy is marked by the resumed growth of the bud.","definition_xrefs":["GOC:PO_curators","PO_REF:00009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dormancy process","termid":"GO:0022611"},{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"bud dormancy process","synonyms":[{"name":"bud dormancy","type":"related"}],"termid":"GO:0097207"}


id: PBO:0072276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S23 pseudogene 5","termid":"PBO:0072276"}


id: MONDO:0009786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"optic atrophy 6","secondary_identifiers":["Orphanet:99012","UMLS:C1850281","GARD:10200","MESH:C537127","MEDGEN:338012","DOID:0111435","OMIM:258500"],"synonyms":[{"name":"OPA6","type":"exact"},{"name":"optic atrophy 6","type":"exact"},{"name":"optic atrophy, congenital or early infantile, autosomal recessive","type":"related"}],"termid":"MONDO:0009786","xrefs":{"Monarch":{"xref_id":"0009786"}}}


id: GO:0047330
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-D-glucose + long chain polyphosphate = glucose-6-phosphate + long chain polyphosphate.","definition_xrefs":["EC:2.7.1.63","MetaCyc:2.7.1.63-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016301","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"polyphosphate-glucose phosphotransferase activity","secondary_identifiers":["RHEA:22036"],"synonyms":[{"name":"polyphosphate glucokinase activity","type":"related"},{"name":"polyphosphate-D-(+)-glucose-6-phosphotransferase activity","type":"related"},{"name":"polyphosphate-glucose 6-phosphotransferase activity","type":"related"},{"name":"polyphosphate:D-glucose 6-phosphotransferase activity","type":"related"}],"termid":"GO:0047330"}


id: MONDO:0800457
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neurodevelopmental disorder in which the cause of the disease is a variation in the HNRNPC gene. It is characterized by global developmental delay, intellectual disability, behavioral abnormalities, and subtle facial dysmorphism. It is caused by heterozygous HNRNPC germline variants.","definition_xrefs":["PMID:37541189","MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"HNRNPC-related neurodevelopmental disorder","termid":"MONDO:0800457","xrefs":{"Monarch":{"xref_id":"0800457"}}}


id: PBO:0059224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maestro heat like repeat family member 6","termid":"PBO:0059224"}


id: PBO:0005754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S20 (predicted)","termid":"PBO:0005754"}


id: PBO:0068226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 533","termid":"PBO:0068226"}


id: MONDO:0005664
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infectious disease produced by bacteria of the genus Bartonella.","definition_xrefs":["Wikipedia:Bartonellosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"Bartonellaceae infectious disease","termid":"MONDO:0006924"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bartonellosis","secondary_identifiers":["NCIT:C84586","UMLS:C0004771","MEDGEN:504","DOID:11102","ICD9:088.0","SCTID:266123003","EFO:0007166","ICD10CM:A44","icd11.foundation:1938462328","MESH:D001474"],"synonyms":[{"name":"Bartonella caused disease or disorder","type":"exact"},{"name":"Bartonella disease or disorder","type":"exact"},{"name":"Bartonella infection","type":"exact"},{"name":"Bartonella infectious disease","type":"exact"},{"name":"Rochalimaea infection","type":"related"},{"name":"Rochalimaea infection (disorder)","type":"exact"},{"name":"Rochalimaea infections","type":"related"},{"name":"bartonelliasis","type":"exact"}],"termid":"MONDO:0005664","xrefs":{"Monarch":{"xref_id":"0005664"}}}


id: PBO:0088420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterol transfer protein Osh3","termid":"PBO:0088420"}


id: MONDO:0022202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"locational disease characteristic","termid":"MONDO:0045040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disseminated","termid":"MONDO:0022202","xrefs":{"Monarch":{"xref_id":"0022202"}}}


id: GO:0010833
data:
  {"annotated_genes":["SJAG_03092","SJAG_02194","SJAG_03855","SJAG_01677","SJAG_00939","SJAG_04586","SJAG_05979","SJAG_03685","SJAG_01378","SJAG_01864","SJAG_02212","SJAG_04266"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74494,80115,92162],"is_not":false,"summary":null,"term":"GO:0010833"},{"annotations":[77222],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032210"},{"annotations":[114155,70927,116276,69959,80612,80570,90964,108438],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007004"}]},"cv_name":"biological_process","definition":"Any process that contributes to the maintenance of proper telomeric length and structure by affecting and monitoring the activity of telomeric proteins and lengthening the telomeric DNA.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomere maintenance","termid":"GO:0000723"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00939":null,"SJAG_01378":null,"SJAG_01677":null,"SJAG_01864":null,"SJAG_02194":null,"SJAG_02212":null,"SJAG_03092":null,"SJAG_03685":null,"SJAG_03855":null,"SJAG_04266":null,"SJAG_04586":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0032200"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0032200","GO:0008150"],"is_obsolete":false,"name":"telomere maintenance via telomere lengthening","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0010833","terms_by_termid":{"GO:0007004":null,"GO:0010833":null,"GO:0032210":null}}


id: MONDO:0007836
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"IVIC syndrome is a very rare genetic malformation syndrome characterized by upper limb anomalies (radial ray defects, carpal bone fusion), extraocular motor disturbances, and congenital bilateral non-progressive mixed hearing loss.","definition_xrefs":["Orphanet:2307"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"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":"IVIC syndrome","secondary_identifiers":["MEDGEN:233003","DOID:0111381","SCTID:722019000","UMLS:C1327918","OMIM:147750","MESH:C535544","GARD:269"],"synonyms":[{"name":"IVIC syndrome","type":"exact"},{"name":"Instituto venezolano de Investigaciones Cientificas syndrome","type":"related"},{"name":"OORS","type":"related"},{"name":"oculo-oto-radial syndrome","type":"exact"},{"name":"oculootoradial syndrome","type":"related"},{"name":"radial Ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia","type":"related"},{"name":"radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia","type":"exact"}],"termid":"MONDO:0007836","xrefs":{"Monarch":{"xref_id":"0007836"}}}


id: GO:0009628
data:
  {"annotated_genes":["SJAG_03319","SJAG_01648","SJAG_05242","SJAG_04388","SJAG_02860","SJAG_05197","SJAG_02199","SJAG_04018","SJAG_02828","SJAG_02818","SJAG_02592","SJAG_03949","SJAG_01584","SJAG_03898","SJAG_02182","SJAG_03345","SJAG_04082","SJAG_01186","SJAG_04055","SJAG_02426","SJAG_00409","SJAG_02091","SJAG_04187","SJAG_02883","SJAG_04150","SJAG_03815","SJAG_04726","SJAG_00272","SJAG_00661","SJAG_04877","SJAG_04567","SJAG_04205","SJAG_02258","SJAG_04190","SJAG_00863","SJAG_01150","SJAG_00642","SJAG_04791","SJAG_01262","SJAG_02334","SJAG_03185","SJAG_02266","SJAG_00436","SJAG_01084","SJAG_04668","SJAG_00729","SJAG_00814","SJAG_02200","SJAG_03893","SJAG_02342","SJAG_01585","SJAG_03527","SJAG_00208","SJAG_00221","SJAG_00596","SJAG_01010","SJAG_02381"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[66573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009785"},{"annotations":[104635,79387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070370"},{"annotations":[92725],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071474"},{"annotations":[119670,119669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071483"},{"annotations":[89835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071473"},{"annotations":[96012,89164,115828,105605,110329,91135,115829,96803,100861,105321,110330,92408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034605"},{"annotations":[112041,117314,101542,110175],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[94688,117407,114795,106826,92211,96292,103112,110670,116612,104848],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071470"},{"annotations":[100497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071472"},{"annotations":[91136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071502"},{"annotations":[108769],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050982"},{"annotations":[95561,103146,109431,77227],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[73524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031990"},{"annotations":[89584,116719],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1900039"},{"annotations":[78307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009314"},{"annotations":[79949,110338],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009651"},{"annotations":[106272,69179,60307,104545,65057,96339,67860,70429,97444,66643,66001,88332,75989,93988,113160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070914"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an abiotic (not derived from living organisms) stimulus.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to 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to abiotic stimulus","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:23873862":null},"synonyms":[{"name":"response to abiotic stress","type":"narrow"}],"termid":"GO:0009628","terms_by_termid":{"GO:0009314":null,"GO:0009651":null,"GO:0009785":null,"GO:0031990":null,"GO:0034605":null,"GO:0050982":null,"GO:0070370":null,"GO:0070914":null,"GO:0071456":null,"GO:0071470":null,"GO:0071472":null,"GO:0071473":null,"GO:0071474":null,"GO:0071483":null,"GO:0071502":null,"GO:1900039":null,"GO:1904161":null}}


id: GO:0103007
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: indole-3-acetate + S-adenosyl-L-methionine = methyl (indol-3-yl)acetate + S-adenosyl-L-homocysteine.","definition_xrefs":["GOC:pz","EC:2.1.1.278"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016741","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"indole-3-acetate carboxyl methyltransferase activity","secondary_identifiers":["RHEA:36131","MetaCyc:RXN-9825"],"termid":"GO:0103007"}


id: GO:0070795
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of conidiophore development, a process that leads to the formation of a conidiophore. The conidiophore is a specialized hypha that extends aerially from the growth substrate and bears conidia, or asexual spores.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of conidiophore development","termid":"GO:0070793"},{"relation_name":"is_a","term_name":"positive regulation of spore-bearing organ development","termid":"GO:0075261"},{"relation_name":"positively_regulates","term_name":"conidiophore development","termid":"GO:0070787"}],"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 conidiophore development","termid":"GO:0070795"}


id: GO:0031946
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of glucocorticoids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucocorticoid metabolic process","termid":"GO:0031943"},{"relation_name":"is_a","term_name":"regulation of steroid hormone biosynthetic process","termid":"GO:0090030"},{"relation_name":"regulates","term_name":"glucocorticoid biosynthetic process","termid":"GO:0006704"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of glucocorticoid biosynthetic process","termid":"GO:0031946"}


id: MONDO:0008163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic developmental defect during embryogenesis characterized by distinct facial features (long triangular face, broad forehead, narrow nose and mandible, high arched palate), prominent, dysmorphic ears (low-set and cup-shaped with large conchae and hypoplastic tragus, antitragus and lobe), long neck, preauricular and/or branchial fistulas and/or cysts, hypoplastic cervical muscles with sloping shoulders and clavicles, winged, low, and laterally-set scapulae, hearing impairment and mild intellectual deficit. Vertebral defects and short stature may also be associated.","definition_xrefs":["Orphanet:2792"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mandibulofacial dysostosis","termid":"MONDO:0015483"},{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otofaciocervical syndrome","secondary_identifiers":["MEDGEN:322257","GARD:4169","MESH:C537074","MESH:C563481","OMIMPS:166780","UMLS:C1833691"],"synonyms":[{"name":"Fara Chlupackova syndrome","type":"exact"},{"name":"Fara-Chlupackova syndrome","type":"exact"},{"name":"OFC syndrome","type":"exact"},{"name":"familial oto-facio-cervical dysmorphia","type":"related"}],"termid":"MONDO:0008163","xrefs":{"Monarch":{"xref_id":"0008163"}}}


id: MONDO:0019798
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acute hepatic porphyria (obsolete MONDO:0019798)","termid":"MONDO:0019798","xrefs":{"Monarch":{"xref_id":"0019798"}}}


id: PBO:0111379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clr6 histone deacetylase complex, chromodomain subunit Alp13/Eaf3","termid":"PBO:0111379"}


id: PBO:0070426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribulose-5-phosphate-3-epimerase pseudogene 4","termid":"PBO:0070426"}


id: PBO:0055730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM domain only 4","termid":"PBO:0055730"}


id: PBO:0085896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; localizes to the cytoplasm and nucleus; overexpression affects protein trafficking through the endocytic pathway","termid":"PBO:0085896"}


id: SO:0000880
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute describing a sequence that contains the code for more than one gene product.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_attribute","termid":"SO:0000237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polycistronic","termid":"SO:0000880"}


id: MONDO:0011558
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of Usher syndrome type 2 that features a heterozygous frameshift mutation in the GPR98 gene and a heterozygous frameshift mutation in the PDZD7 gene. It is inherited in an autosomal recessive manner.","definition_xrefs":["OMIM:605472"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Usher syndrome type 2","termid":"MONDO:0016484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Usher syndrome type 2C","secondary_identifiers":["DOID:0110839","GARD:8497","MEDGEN:419359","NCIT:C153174","ICD10CM:H35.5","MESH:C536492","UMLS:C2931213"],"synonyms":[{"name":"USH2C","type":"exact"},{"name":"USHER syndrome, type IIC","type":"related"},{"name":"Usher syndrome type IIC","type":"exact"},{"name":"Usher syndrome, type 2C","type":"related"},{"name":"Usher syndrome, type 2C, GPR98/PDZD7 digenic, autosomal recessive, digenic dominant","type":"exact"},{"name":"Usher syndrome, type 2C, autosomal recessive, digenic dominant","type":"exact"},{"name":"Usher syndrome, type IIC, GPR98/PDZD7 digenic, autosomal recessive, digenic dominant","type":"exact"},{"name":"Usher syndrome, type IIb","type":"related"},{"name":"Usher syndrome, type IIb, formerly","type":"related"},{"name":"Usher syndrome, type IIc, Gpr98/Pdzd7, digenic","type":"related"}],"termid":"MONDO:0011558","xrefs":{"Monarch":{"xref_id":"0011558"}}}


id: GO:0060095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of glycinergic synaptic transmission in the presence of zinc. Glycinergic synaptic transmission is the process of communication from a neuron to another neuron across a synapse using the neurotransmitter glycine.","definition_xrefs":["GOC:dms","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of synaptic transmission, glycinergic","termid":"GO:0060094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"zinc potentiation of synaptic transmission, glycinergic","synonyms":[{"name":"zinc potentiation of glycinergic synaptic transmission","type":"exact"}],"termid":"GO:0060095"}


id: PBO:0078622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 71","termid":"PBO:0078622"}


id: PATO:0001706
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A behavioral quality inhering in a bearer by virtue of the bearer's disposition to lack activity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavioural activity","termid":"PATO:0002265"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"behavioural inactive","termid":"PATO:0001706"}


id: MONDO:0008353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"urticaria","termid":"MONDO:0005492"},{"relation_name":"is_a","term_name":"pregnancy disorder","termid":"MONDO:0024575"}],"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":"pruritic urticarial papules and plaques of pregnancy","secondary_identifiers":["UMLS:C0269680","MESH:C535817","icd11.foundation:968694549","ICD9:646.80","MedDRA:10066100","GARD:9635","MEDGEN:78710","ICD9:692.9","Orphanet:64745","OMIM:178995","SCTID:88697005"],"synonyms":[{"name":"PUPPP","type":"related"},{"name":"polymorphic eruption of pregnancy","type":"exact"},{"name":"pruritic urticarial papules and plaques of pregnancy","type":"exact"},{"name":"pruritic urticarial papules and plaques of pregnancy, familial (subtype)","type":"related"},{"name":"pruritic urticarial papules plaques of pregnancy","type":"related"}],"termid":"MONDO:0008353","xrefs":{"Monarch":{"xref_id":"0008353"}}}


id: PBO:0043997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chorionic somatomammotropin hormone 2","termid":"PBO:0043997"}


id: GO:1905237
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 cyclosporin A stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:24914722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cyclosporin A","synonyms":[{"name":"response to cyclophilin","type":"exact"}],"termid":"GO:1905237"}


id: GO:0009528
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The inner, i.e. lumen-facing, lipid bilayer of the plastid envelope; also faces the plastid stroma.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle inner membrane","termid":"GO:0019866"},{"relation_name":"is_a","term_name":"plastid membrane","termid":"GO:0042170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"plastid inner membrane","termid":"GO:0009528"}


id: GO:0070657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regrowth of a neuromast following its loss or destruction.","definition_xrefs":["GOC:dsf","PMID:19381250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mechanosensory epithelium regeneration","termid":"GO:0070655"}],"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":"neuromast regeneration","termid":"GO:0070657"}


id: PBO:0002684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylyl-sulfate kinase (predicted)","termid":"PBO:0002684"}


id: MONDO:0016459
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The newly described 2q23.1 microdeletion syndrome includes severe intellectual deficit with pronounced speech delay, behavioral abnormalities including hyperactivity and inappropriate laughter, short stature and seizures.","definition_xrefs":["Orphanet:228402"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"epilepsy","termid":"MONDO:0005027"},{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 2","termid":"MONDO:0016901"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2q23.1 microdeletion syndrome","secondary_identifiers":["MEDGEN:930201","SCTID:719657001","UMLS:C4304532","GARD:10998"],"synonyms":[{"name":"Del(2)(q23.1)","type":"exact"},{"name":"chromosome 2q23.1 microdeletion syndrome","type":"related"},{"name":"monosomy 2q23.1","type":"exact"},{"name":"pseudo-Angelman syndrome","type":"exact"}],"termid":"MONDO:0016459","xrefs":{"Monarch":{"xref_id":"0016459"}}}


id: PBO:0087395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S/T protein kinase; required for PM lipid and protein homeostasis; involved in sphingolipid-mediated and cell integrity signaling pathways and endocytosis; phosphorylates and downregulates Fpk1p; phosphorylates and inactivates Orm1p/2p when sphingolipid synthesis is compromised; role in TORC1/2-dependent Rps6a/b phosphorylation; phosphorylated and activated by TORC2 and by Pkh1/2p in the presence of phytosphingosine; human homolog SGK1 complements the null and inviability of a ypk1 ypk2 mutant","termid":"PBO:0087395"}


id: PBO:0116749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF related BAF chromatin remodeling complex subunit C1","termid":"PBO:0116749"}


id: FYECO:0000110
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells are first grown in minimal medium lacking nitrogen and are then allowed to recover in rich medium.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping sequential growth conditions","termid":"FYECO:0000094"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nitrogen starvation and recovery","synonyms":[{"name":"recovery from nitrogen depletion","type":"exact"},{"name":"recovery from nitrogen starvation","type":"exact"}],"termid":"FYECO:0000110"}


id: MONDO:0015669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disease with dentinogenesis imperfecta (obsolete MONDO:0015669)","secondary_identifiers":["Orphanet:167762"],"termid":"MONDO:0015669","xrefs":{"Monarch":{"xref_id":"0015669"}}}


id: FYPO:0007665
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which a cell is viable, and contains one nucleus and one septum. The septum divides the cell into two compartments, one of which contains the nucleus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable vegetative cell","termid":"FYPO:0001491"},{"relation_name":"is_a","term_name":"mononucleate monoseptate vegetative cell with anucleate compartment","termid":"FYPO:0007664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000004"],"is_obsolete":false,"name":"viable mononucleate monoseptate vegetative cell with anucleate compartment","synonyms":[{"name":"displaced nucleus with septum","type":"related"},{"name":"viable mononucleate monoseptate cell during vegetative growth","type":"exact"},{"name":"viable mononucleate monoseptate vegetative cell","type":"exact"},{"name":"viable mononucleate monoseptate vegetative cell during mitotic cell cycle","type":"related"},{"name":"viable with septation in the absence of nuclear division","type":"related"},{"name":"viable with septation independent of mitosis","type":"related"},{"name":"viable with septation without nuclear division","type":"related"}],"termid":"FYPO:0007665"}


id: GO:0043478
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation of coloring matter in a particular location in an organism, tissue or cell, occurring in response to a UV light stimulus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to UV","termid":"GO:0009411"},{"relation_name":"is_a","term_name":"pigment accumulation","termid":"GO:0043476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"pigment accumulation in response to UV light","termid":"GO:0043478"}


id: PBO:0108557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Esf1","termid":"PBO:0108557"}


id: MONDO:0012563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any holoprosencephaly in which the cause of the disease is a mutation in the GLI2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microform holoprosencephaly","termid":"MONDO:0017219"},{"relation_name":"is_a","term_name":"lobar holoprosencephaly","termid":"MONDO:0019756"},{"relation_name":"is_a","term_name":"alobar holoprosencephaly","termid":"MONDO:0019757"}],"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":"holoprosencephaly 9","secondary_identifiers":["DOID:0110873","MEDGEN:324369","UMLS:C1835819","OMIM:610829"],"synonyms":[{"name":"GLI2 holoprosencephaly","type":"exact"},{"name":"HPE9","type":"exact"},{"name":"holoprosencephaly 9","type":"exact"},{"name":"holoprosencephaly caused by mutation in GLI2","type":"exact"},{"name":"holoprosencephaly type 9","type":"exact"},{"name":"holoprosencephaly with microphthalmia and first branchial Arch anomalies","type":"related"},{"name":"holoprosencephaly with microphthalmia and first branchial arch anomalies","type":"exact"},{"name":"pituitary anomalies with holoprosencephaly-like features","type":"exact"}],"termid":"MONDO:0012563","xrefs":{"Monarch":{"xref_id":"0012563"}}}


id: GO:0034053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a symbiont modulates the frequency, rate or extent of defense-related programmed cell death in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete symbiont-mediated perturbation of host defense-related programmed cell death (obsolete GO:0034053)","synonyms":[{"name":"modulation by symbiont of host HR","type":"narrow"},{"name":"modulation by symbiont of host defense-related PCD","type":"exact"},{"name":"modulation by symbiont of host defense-related programmed cell death","type":"exact"},{"name":"modulation by symbiont of host hypersensitive response","type":"narrow"},{"name":"modulation by symbiont of plant HR","type":"narrow"},{"name":"modulation by symbiont of plant hypersensitive response","type":"narrow"}],"termid":"GO:0034053"}


id: PBO:0064553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POM121 transmembrane nucleoporin like 15, pseudogene","termid":"PBO:0064553"}


id: GO:0102588
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cyanidin 3-O-beta-D-glucoside betaine + malonyl-CoA = cyanidin 3-O-(6-O-malonyl-beta-D-glucoside) + coenzyme A.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete cyanidin 3-O-glucoside 6''-O-malonyltransferase activity (obsolete GO:0102588)","termid":"GO:0102588"}


id: FYPO:0001046
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cells enter mitosis earlier, relative to cell size or DNA integrity checkpoint status, than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mistimed mitosis","termid":"FYPO:0001204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000337"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000337","FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"premature mitosis","synonyms":[{"name":"advanced mitosis","type":"exact"},{"name":"early mitosis","type":"exact"},{"name":"premature mitosis during mitotic cell cycle","type":"related"},{"name":"premature mitosis during vegetative growth","type":"exact"}],"termid":"FYPO:0001046"}


id: PBO:0040681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain enriched myelin associated protein 1","termid":"PBO:0040681"}


id: PBO:0049177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth regulating estrogen receptor binding 1","termid":"PBO:0049177"}


id: FYPO:0006717
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 sodium chloride, usually at a higher level than in standard media.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000003","FYPO:0002060","FYPO:0002058","FYPO:0000257","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on sodium chloride","synonyms":[{"name":"normal cell population growth in presence of sodium chloride","type":"exact"},{"name":"normal cell population growth on sodium chloride","type":"exact"},{"name":"normal cellular response to sodium chloride","type":"related"},{"name":"normal growth on NaCl","type":"exact"},{"name":"normal vegetative cell population growth on sodium chloride","type":"exact"}],"termid":"FYPO:0006717"}


id: PBO:0012610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-amino-5-hydroxymethyl-2-methylpyrimidine phosphate synthase Nmt1","termid":"PBO:0012610"}


id: PBO:0064434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PNP pseudogene 1","termid":"PBO:0064434"}


id: PBO:0085716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in SRP-independent targeting of substrates to the ER; component of an alternative ER targeting pathway that has partial functional redundancy with the GET pathway; preference for substrates with downstream transmembrane domains; interacts with Env10p/Snd2p and Pho88p/Snd3p; can compensate for loss of SRP; co-purifies with ribosomes; GFP-fusion protein localizes to the cytoplasm","termid":"PBO:0085716"}


id: MONDO:0011654
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism","secondary_identifiers":["MEDGEN:342889","MESH:C565246","UMLS:C1853480","OMIM:606242"],"synonyms":[{"name":"Kondoh syndrome","type":"related"},{"name":"intellectual disability, microcephaly, growth retardation, JOINT contractures, and facial dysmorphism","type":"related"},{"name":"mental retardation, microcephaly, growth retardation, JOINT contractures, and facial dysmorphism","type":"related"}],"termid":"MONDO:0011654","xrefs":{"Monarch":{"xref_id":"0011654"}}}


id: PBO:0084473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MATalpha-specific a-factor blocker; contributes to mating efficiency under certain conditions; localizes to the cell wall; predicted to be a GPI-attached protein; upregulated by Mcm1p-Alpha1p transcription factor; partially overlaps the dubious ORF YLR041W","termid":"PBO:0084473"}


id: PR:Q9P6I8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An uncharacterized zinc-type alcohol dehydrogenase-like protein YbdR that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02347","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":"zinc-type alcohol dehydrogenase-like protein C1198.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.01","secondary_identifiers":["UniProtKB:Q9P6I8"],"synonyms":[{"name":"Spom972h-ybdR","type":"exact"}],"termid":"PR:Q9P6I8"}


id: PBO:0005368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE Psy1","termid":"PBO:0005368"}


id: PR:O94288
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nucleolar complex protein 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03754","PRO:DNx","PANTHER:PTHR14428:SF5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar complex-associated protein 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC887.03c","secondary_identifiers":["UniProtKB:O94288"],"synonyms":[{"name":"Spom972h-NOC3L","type":"exact"}],"termid":"PR:O94288"}


id: PBO:0056610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malic enzyme 2 pseudogene 1","termid":"PBO:0056610"}


id: PBO:0077206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane 6 superfamily member 1","termid":"PBO:0077206"}


id: FYPO:0008025
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed during mitotic M-phase in which the localization of a protein to the CENP-A containing chromatin is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:35970865","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to CENP-A containing chromatin","termid":"FYPO:0004314"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to CENP-A containing chromatin during mitosis","synonyms":[{"name":"normal protein localization to CENP-A containing chromatin during mitotic M-phase","type":"exact"},{"name":"normal protein localization to centromeric core region chromatin during mitosis","type":"exact"}],"termid":"FYPO:0008025"}


id: PBO:0065068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich protein HaeIII subfamily 2","termid":"PBO:0065068"}


id: GO:0097449
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A prolongation or process extending from the soma of an astrocyte and wrapping around neurons.","definition_xrefs":["NIF_Subcellular:sao1630537580"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell projection","termid":"GO:0097386"}],"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":"astrocyte projection","synonyms":[{"name":"astrocyte process","type":"exact"},{"name":"peripheral astrocyte process","type":"related"},{"name":"vellous process","type":"related"}],"termid":"GO:0097449"}


id: MONDO:0005803
data:
  {"annotated_genes":["SJAG_04334","SJAG_00154","SJAG_03266","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859362"},{"annotations":[86817,86818],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011236"},{"annotations":[87146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011717"}]},"cv_name":"mondo","definition":"An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the pancreas and congenital hyperinsulinism. It is due to focal hyperplasia of pancreatic islet cells budding off from the ductal structures and forming new islets of langerhans. Mutations in the islet cells involve the potassium channel gene kcnj11 or the atp-binding cassette transporter gene abcc8, both on chromosome 11.","definition_xrefs":["MESH:D046768"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"relation_name":"is_a","term_name":"inborn carbohydrate metabolic disorder","termid":"MONDO:0019214"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00154":null,"SJAG_03266":null,"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"hyperinsulinemic hypoglycemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["HP:0000825","OMIMPS:256450","GARD:21849","DOID:13317","SCTID:42681006","NANDO:2100143","NCIT:C4375","UMLS:C1864903","EFO:0007318","MEDGEN:351247","NANDO:2200399","Orphanet:443095"],"synonyms":[{"name":"hyperinsulinemia hypoglycemia","type":"exact"},{"name":"hyperinsulinemic hypoglycemia (disease)","type":"exact"},{"name":"islet cell hyperplasia","type":"exact"},{"name":"nesidioblastosis","type":"related"},{"name":"persistent hyperinsulinemia hypoglycemia of infancy","type":"exact"}],"termid":"MONDO:0005803","terms_by_termid":{"MONDO:0011236":null,"MONDO:0011717":null,"MONDO:0859362":null},"xrefs":{"Monarch":{"xref_id":"0005803"}}}


id: PBO:0089879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane protein complex subunit Emc4","termid":"PBO:0089879"}


id: PBO:0060183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucin 3B, cell surface associated","termid":"PBO:0060183"}


id: PBO:0045639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 51 (pseudogene)","termid":"PBO:0045639"}


id: PBO:0110346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDCA7 pseudogene 2","termid":"PBO:0110346"}


id: MONDO:0010460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intellectual disability-alacrima-achalasia syndrome is a rare, genetic intellectual disability syndrome characterized by delayed motor and cognitive development, absence or severe delay in speech development, intellectual disability, and alacrima. Achalasia/dysphagia and mild autonomic dysfunction (i.e. anisocoria) have also been reported in some patients. The phenotype is similar to the one observed in autosomal recessive Triple A syndrome, but differs by the presence of intellectual disability in all affected individuals.","definition_xrefs":["Orphanet:289483"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndromic X-linked intellectual disability 17","secondary_identifiers":["DOID:0060803","MEDGEN:477091","GARD:17326","OMIM:300858","UMLS:C3275460"],"synonyms":[{"name":"MRXS17","type":"related"},{"name":"X-linked intellectual disability with alacrima and achalasia","type":"exact"},{"name":"X-linked mental retardation with alacrima and achalasia","type":"exact"},{"name":"intellectual disability, X-linked, syndromic 17","type":"exact"},{"name":"intellectual disability, X-linked, with alacrima and achalasia","type":"related"},{"name":"intellectual disability-alacrima-achalasia syndrome","type":"exact"},{"name":"mental retardation, X-linked, syndromic 17","type":"exact"},{"name":"mental retardation, X-linked, syndromic 17, X-linked recessive","type":"exact"},{"name":"mental retardation, X-linked, with alacrima and achalasia","type":"related"},{"name":"syndromic X-linked intellectual disability type 17","type":"exact"}],"termid":"MONDO:0010460","xrefs":{"Monarch":{"xref_id":"0010460"}}}


id: FYPO:0000414
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype in which plasma membrane fusion involved in cytogamy is decreased.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete decreased cell fusion during mating (obsolete FYPO:0000414)","synonyms":[{"name":"cell fusion: decreased","type":"related"},{"name":"decreased cell fusion during conjugation","type":"exact"},{"name":"decreased plasma membrane fusion involved in cytogamy","type":"exact"},{"name":"reduced cell fusion during mating","type":"exact"}],"termid":"FYPO:0000414"}


id: PBO:0033820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"substrate-specific mitotic G1 APC coactivator Srw1/Ste9","termid":"PBO:0033820"}


id: PBO:0040846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"biogenesis of lysosomal organelles complex 1 subunit 1","termid":"PBO:0040846"}


id: FYPO:0003917
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the degradation of messenger RNA (mRNA) molecules that contain nonsense mutations is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA catabolic process during vegetative growth","termid":"FYPO:0002137"},{"relation_name":"is_a","term_name":"abnormal nonsense-mediated decay","termid":"FYPO:0003916"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0000294","FYPO:0006551"],"is_obsolete":false,"name":"decreased nonsense-mediated decay","synonyms":[{"name":"decreased NMD","type":"exact"},{"name":"decreased nonsense-mediated decay during mitotic cell cycle","type":"related"},{"name":"decreased nonsense-mediated decay during vegetative growth","type":"exact"},{"name":"decreased nuclear-transcribed mRNA catabolic process, nonsense-mediated decay","type":"exact"},{"name":"reduced nonsense-mediated decay","type":"exact"}],"termid":"FYPO:0003917"}


id: PBO:0116984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FOS antisense RNA 1","termid":"PBO:0116984"}


id: PBO:0064007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 41","termid":"PBO:0064007"}


id: PR:P05764
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 40S ribosomal protein S21 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03124","PANTHER:PTHR10442:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18E5.06","secondary_identifiers":["UniProtKB:P05764"],"synonyms":[{"name":"S28 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-RPS21","type":"exact"}],"termid":"PR:P05764"}


id: PR:Q9P371
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sst2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P371"],"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":"AMSH-like protease sst2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19B12.10","synonyms":[{"name":"Spom972h-sst2","type":"exact"},{"name":"suppressor of ste12 deletion protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P371"}


id: MONDO:0010399
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn glycerol kinase deficiency","termid":"MONDO:0010613"},{"relation_name":"is_a","term_name":"partial monosomy of the short arm of chromosome X","termid":"MONDO:0017004"}],"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":"chromosome Xp21 deletion syndrome","secondary_identifiers":["ICD9:277.6","SCTID:297257004","Orphanet:261476","MEDGEN:1373978","UMLS:C4505291","DOID:0060427","OMIM:300679","GARD:17246"],"synonyms":[{"name":"Complex Glycerol kinase deficiency","type":"related"},{"name":"Del(X)(p21)","type":"exact"},{"name":"Glycerol kinase deficiency-contiguous gene syndrome","type":"exact"},{"name":"Xp21 contiguous gene deletion syndrome","type":"exact"},{"name":"Xp21 microdeletion syndrome","type":"exact"},{"name":"chromosome Xp21 deletion syndrome","type":"exact"},{"name":"complex glycerol kinase deficiency","type":"exact"},{"name":"monosomy Xp21","type":"exact"}],"termid":"MONDO:0010399","xrefs":{"Monarch":{"xref_id":"0010399"}}}


id: GO:0009220
data:
  {"annotated_genes":["SJAG_04713","SJAG_04354","SJAG_03164","SJAG_05024","SJAG_00533","SJAG_00779","SJAG_02887","SJAG_00444","SJAG_00197","SJAG_03708","SJAG_00694","SJAG_04709","SJAG_00964"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044210"},{"annotations":[57233,59498,61990,61234,59164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044205"},{"annotations":[80736],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046705"},{"annotations":[68203],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009224"},{"annotations":[64613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006241"},{"annotations":[93295,68205],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044211"},{"annotations":[80738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006225"},{"annotations":[68204,87779,88771,92293,93296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044206"},{"annotations":[64612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006228"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a pyrimidine ribonucleotide, a compound consisting of nucleoside (a pyrimidine base linked to a ribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleotide biosynthetic process","termid":"GO:0006221"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide metabolic process","termid":"GO:0009218"},{"relation_name":"is_a","term_name":"ribonucleotide biosynthetic process","termid":"GO:0009260"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00444":null,"SJAG_00533":null,"SJAG_00694":null,"SJAG_00779":null,"SJAG_00964":null,"SJAG_02887":null,"SJAG_03164":null,"SJAG_03708":null,"SJAG_04354":null,"SJAG_04709":null,"SJAG_04713":null,"SJAG_05024":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"pyrimidine ribonucleotide biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["MetaCyc:PWY0-162"],"synonyms":[{"name":"pyrimidine ribonucleotide anabolism","type":"exact"},{"name":"pyrimidine ribonucleotide biosynthesis","type":"exact"},{"name":"pyrimidine ribonucleotide formation","type":"exact"},{"name":"pyrimidine ribonucleotide synthesis","type":"exact"}],"termid":"GO:0009220","terms_by_termid":{"GO:0006225":null,"GO:0006228":null,"GO:0006241":null,"GO:0009224":null,"GO:0044205":null,"GO:0044206":null,"GO:0044210":null,"GO:0044211":null,"GO:0046705":null}}


id: PBO:0055586
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 3022","termid":"PBO:0055586"}


id: GO:0034697
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 prostagladin I stimulus.","definition_xrefs":["GOC:vk","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to prostaglandin","termid":"GO:0034694"},{"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 prostaglandin I","synonyms":[{"name":"response to prostaglandin I stimulus","type":"exact"}],"termid":"GO:0034697"}


id: PBO:0080126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicle associated membrane protein 4","termid":"PBO:0080126"}


id: FYECO:0000457
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which the Type 4 phosphodiesterase (PDE4) inhibitor rolipram was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ rolipram","termid":"FYECO:0000457"}


id: PBO:0068208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 515","termid":"PBO:0068208"}


id: MONDO:0003674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An electrocardiographic finding of an injury in leads corresponding to the anatomic region of the subendocardial layer of the wall of the heart.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myocardial infarction","termid":"MONDO:0005068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"subendocardial myocardial infarction","secondary_identifiers":["MEDGEN:75500","DOID:5849","UMLS:C0262568"],"synonyms":[{"name":"myocardial infarction (disease) of subendocardium layer","type":"exact"},{"name":"subendocardium layer myocardial infarction (disease)","type":"exact"}],"termid":"MONDO:0003674","xrefs":{"Monarch":{"xref_id":"0003674"}}}


id: PBO:0065281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich and Gla domain 1","termid":"PBO:0065281"}


id: GO:2000613
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of thyroid-stimulating hormone secretion.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of peptide hormone secretion","termid":"GO:0090278"},{"relation_name":"is_a","term_name":"regulation of thyroid-stimulating hormone secretion","termid":"GO:2000612"},{"relation_name":"negatively_regulates","term_name":"thyroid-stimulating hormone secretion","termid":"GO:0070460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"negative regulation of thyroid-stimulating hormone secretion","synonyms":[{"name":"negative regulation of TSH secretion","type":"exact"},{"name":"negative regulation of thyroid stimulating hormone secretion","type":"exact"}],"termid":"GO:2000613"}


id: GO:0035193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Reorganization of the pre-existing, functional larval central nervous system into one that can serve the novel behavioral needs of the adult. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["GOC:sensu","PMID:9647692"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"instar larval or pupal development","termid":"GO:0002165"},{"relation_name":"part_of","term_name":"central nervous system development","termid":"GO:0007417"}],"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":"larval central nervous system remodeling","synonyms":[{"name":"CNS metamorphosis","type":"exact"},{"name":"central nervous system metamorphosis","type":"exact"},{"name":"larval central nervous system remodelling","type":"exact"}],"termid":"GO:0035193"}


id: PBO:0080075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 38","termid":"PBO:0080075"}


id: PBO:0045213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C6","termid":"PBO:0045213"}


id: MOD:00095
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamine residue to L-glutamine amide.","definition_xrefs":["PubMed:7673220","PubMed:9048550","RESID:AA0086"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-glutamine residue","termid":"MOD:00907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-glutamine amide","synonyms":[{"name":"(2S)-2-aminopentanediamide","type":"exact"},{"name":"GlnN","type":"exact"},{"name":"L-glutamine amide","type":"exact"},{"name":"MOD_RES Glutamine amide","type":"exact"},{"name":"amidated L-glutamine","type":"exact"},{"name":"glutaminamide","type":"exact"}],"termid":"MOD:00095"}


id: PBO:0084236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Imidazoleglycerol-phosphate dehydratase; catalyzes the sixth step in histidine biosynthesis; mutations cause histidine auxotrophy and sensitivity to Cu, Co, and Ni salts; transcription is regulated by general amino acid control via Gcn4p","termid":"PBO:0084236"}


id: GO:0098004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a virus tail fiber.","definition_xrefs":["VZ:3956","GOC:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"},{"relation_name":"part_of","term_name":"viral tail assembly","termid":"GO:0098003"}],"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":"virus tail fiber assembly","termid":"GO:0098004"}


id: GO:2000944
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of amylopectin metabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of macromolecule metabolic process","termid":"GO:0010604"},{"relation_name":"is_a","term_name":"regulation of amylopectin metabolic process","termid":"GO:2000942"},{"relation_name":"positively_regulates","term_name":"amylopectin metabolic process","termid":"GO:2000896"}],"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 amylopectin metabolic process","synonyms":[{"name":"positive regulation of Amylopectin metabolism","type":"exact"}],"termid":"GO:2000944"}


id: GO:0018980
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 2,4,5-trichlorophenoxyacetic acid, a chlorinated aromatic compound which is widely used as a herbicide, often as a weed killer for home lawns.","definition_xrefs":["UM-BBD_pathwayID:2,4,5-t"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ether metabolic process","termid":"GO:0018904"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"organohalogen metabolic process","termid":"GO:0090345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"2,4,5-trichlorophenoxyacetic acid metabolic process","secondary_identifiers":["UM-BBD_pathwayID:2\\,4\\,5-t"],"synonyms":[{"name":"2,4,5-T metabolic process","type":"exact"},{"name":"2,4,5-T metabolism","type":"exact"},{"name":"2,4,5-trichlorophenoxyacetic acid metabolism","type":"exact"}],"termid":"GO:0018980"}


id: FYPO:0008178
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 RNAs transcribed from the centromere inner repeat region are present at normal levels (i.e. indistinguishable from wild-type).","direct_ancestors":[{"relation_name":"is_a","term_name":"normal centromeric RNA level during vegetative growth","termid":"FYPO:0008177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal centromeric inner repeat transcript level","termid":"FYPO:0008178"}


id: PBO:0018210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial proton-transporting ATP synthase inhibitor (predicted)","termid":"PBO:0018210"}


id: PBO:0049141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamic--pyruvic transaminase 2","termid":"PBO:0049141"}


id: MONDO:1010476
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent truncus arteriosus that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"persistent truncus arteriosus, non-human animal","termid":"MONDO:1010018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent truncus arteriosus, sheep","secondary_identifiers":["OMIA:000795-9940"],"termid":"MONDO:1010476","xrefs":{"Monarch":{"xref_id":"1010476"}}}


id: GO:1901151
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of vistamycin.","definition_xrefs":["UniPathway:UPA00972","GOC:yaf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoglycoside antibiotic catabolic process","termid":"GO:0030649"},{"relation_name":"is_a","term_name":"polyol catabolic process","termid":"GO:0046174"},{"relation_name":"is_a","term_name":"vistamycin metabolic process","termid":"GO:1901150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"vistamycin catabolic process","synonyms":[{"name":"ribostamycin breakdown","type":"exact"},{"name":"ribostamycin catabolic process","type":"exact"},{"name":"ribostamycin catabolism","type":"exact"},{"name":"ribostamycin degradation","type":"exact"},{"name":"vistamycin breakdown","type":"exact"},{"name":"vistamycin catabolism","type":"exact"},{"name":"vistamycin degradation","type":"exact"}],"termid":"GO:1901151"}


id: PBO:0052029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Jupiter microtubule associated homolog 2","termid":"PBO:0052029"}


id: MONDO:1011498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Enteropathy-associated T cell lymphoma that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-hodgkin lymphoma, domestic cat","termid":"MONDO:1010949"},{"relation_name":"is_a","term_name":"enteropathy-associated T cell lymphoma, non-human animal","termid":"MONDO:1011442"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enteropathy-associated T cell lymphoma, domestic cat","secondary_identifiers":["OMIA:002526-9685"],"termid":"MONDO:1011498","xrefs":{"Monarch":{"xref_id":"1011498"}}}


id: GO:0071369
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 an ethylene (ethene) stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to ethylene","termid":"GO:0009723"},{"relation_name":"is_a","term_name":"cellular response to hormone stimulus","termid":"GO:0032870"}],"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 ethylene stimulus","synonyms":[{"name":"cellular response to ethene stimulus","type":"exact"}],"termid":"GO:0071369"}


id: MONDO:0032617
data:
  {"annotated_genes":["SJAG_03782"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86570],"is_not":false,"summary":null,"term":"MONDO:0032617"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, nuclear type","termid":"MONDO:0100223"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03782":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex 1 deficiency, nuclear type 11","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112089","UMLS:C4748769","GARD:16321","OMIM:618234","MEDGEN:1648356"],"synonyms":[{"name":"MC1DN11","type":"related"},{"name":"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11","type":"related"}],"termid":"MONDO:0032617","terms_by_termid":{"MONDO:0032617":null},"xrefs":{"Monarch":{"xref_id":"0032617"}}}


id: PBO:0042762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 55","termid":"PBO:0042762"}


id: PBO:0082689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the HAT/Core module of the SAGA, SLIK, and ADA complexes; HAT/Core module also contains Gcn5p, Ngg1p, and Ada2p; binds methylated histone H3K4; involved in transcriptional regulation through SAGA and TBP recruitment to target promoters and H3 acetylation","termid":"PBO:0082689"}


id: GO:0120287
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of intramembrane cleaving aspartic-type endopeptidase activity.","definition_xrefs":["GOC:krc","PMID:32616437"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of aspartic endopeptidase activity, intramembrane cleaving (obsolete GO:0120287)","termid":"GO:0120287"}


id: PR:P78958
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A glyceraldehyde-3-phosphate dehydrogenase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03431"],"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":"glyceraldehyde-3-phosphate dehydrogenase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC32F12.11","secondary_identifiers":["UniProtKB:P78958"],"synonyms":[{"name":"GAPDH 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-GAPDH","type":"exact"}],"termid":"PR:P78958"}


id: FYPO:0004488
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the methylation of one or more lysine residues in specific proteins, or at specific protein sites, does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein modification during vegetative growth","termid":"FYPO:0000544"},{"relation_name":"is_a","term_name":"abnormal protein acetylation during vegetative growth","termid":"FYPO:0002392"},{"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:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0002494","FYPO:0001985","FYPO:0002274"],"is_obsolete":false,"name":"abolished protein lysine methylation during vegetative growth","synonyms":[{"name":"abolished peptidyl-lysine methylation during vegetative growth","type":"exact"},{"name":"abolished protein acetylation during mitotic cell cycle","type":"related"},{"name":"protein lysine methylation abolished during vegetative growth","type":"exact"},{"name":"protein lysine methylation absent during vegetative growth","type":"exact"}],"termid":"FYPO:0004488"}


id: GO:1901741
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of myoblast fusion.","definition_xrefs":["GOC:TermGenie","GOC:rl","PMID:21364645","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of syncytium formation by plasma membrane fusion","termid":"GO:0060143"},{"relation_name":"is_a","term_name":"regulation of myoblast fusion","termid":"GO:1901739"},{"relation_name":"positively_regulates","term_name":"myoblast fusion","termid":"GO:0007520"}],"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 myoblast fusion","synonyms":[{"name":"activation of myoblast fusion","type":"narrow"},{"name":"up regulation of myoblast fusion","type":"exact"},{"name":"up-regulation of myoblast fusion","type":"exact"},{"name":"upregulation of myoblast fusion","type":"exact"}],"termid":"GO:1901741"}


id: PBO:0090589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial MIB complex subunit, human DNAJC11 ortholog","termid":"PBO:0090589"}


id: MONDO:0007849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratitis fugax hereditaria","secondary_identifiers":["MESH:C563650","UMLS:C1835697","MEDGEN:372107","OMIM:148200","Orphanet:647815"],"synonyms":[{"name":"KEFH","type":"related"},{"name":"KERATOENDOTHELIITIS fugax hereditaria","type":"related"},{"name":"Keratoendotheliitis fugax hereditaria","type":"related"},{"name":"keratitis fugax hereditaria","type":"exact"},{"name":"keratoendotheliitis fugax hereditaria","type":"exact"},{"name":"keratoendothelitis fugax hereditaria","type":"exact"}],"termid":"MONDO:0007849","xrefs":{"Monarch":{"xref_id":"0007849"}}}


id: GO:0072542
data:
  {"annotated_genes":["SJAG_00369","SJAG_03681","SJAG_01142","SJAG_00078","SJAG_00526","SJAG_00095","SJAG_04638","SJAG_04968","SJAG_03353","SJAG_01270"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73004,74946,76770,79243,93254,98024,115313,118280],"is_not":false,"summary":null,"term":"GO:0072542"},{"annotations":[72038,76098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008160"}]},"cv_name":"molecular_function","definition":"Binds to and increases the activity of a protein phosphatase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activator activity","termid":"GO:0019211"},{"relation_name":"is_a","term_name":"protein phosphatase regulator activity","termid":"GO:0019888"},{"relation_name":"positively_regulates","term_name":"phosphoprotein phosphatase activity","termid":"GO:0004721"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00078":null,"SJAG_00095":null,"SJAG_00369":null,"SJAG_00526":null,"SJAG_01142":null,"SJAG_01270":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04638":null,"SJAG_04968":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"positively_regulates","termid":"GO:0140096"},{"rel_name":"positively_regulates","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"regulates","termid":"GO:0016787"},{"rel_name":"regulates","termid":"GO:0140096"},{"rel_name":"positively_regulates","termid":"GO:0016787"},{"rel_name":"positively_regulates","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"regulates","termid":"GO:0003824"},{"rel_name":"regulates","termid":"GO:0016788"},{"rel_name":"regulates","termid":"GO:0004721"}],"interesting_parent_ids":["GO:0140677","GO:0098772","GO:0016788","GO:0016787","GO:0030234","GO:0140096","GO:0003824","GO:0003674","GO:0004721"],"is_obsolete":false,"name":"protein phosphatase activator activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0072543","GO:0071862"],"synonyms":[{"name":"protein phosphatase 2 activator activity","type":"narrow"},{"name":"protein phosphatase type 1 activator activity","type":"narrow"},{"name":"protein phosphatase type 2A activator activity","type":"narrow"}],"termid":"GO:0072542","terms_by_termid":{"GO:0008160":null,"GO:0072542":null}}


id: GO:0001798
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of type IIa hypersensitivity, a type of inflammatory response.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of type IIa hypersensitivity","termid":"GO:0001796"},{"relation_name":"is_a","term_name":"positive regulation of type II hypersensitivity","termid":"GO:0002894"},{"relation_name":"positively_regulates","term_name":"type IIa hypersensitivity","termid":"GO:0001794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of type IIa hypersensitivity","synonyms":[{"name":"activation of type IIa hypersensitivity","type":"narrow"},{"name":"stimulation of type IIa hypersensitivity","type":"narrow"},{"name":"up regulation of type IIa hypersensitivity","type":"exact"},{"name":"up-regulation of type IIa hypersensitivity","type":"exact"},{"name":"upregulation of type IIa hypersensitivity","type":"exact"}],"termid":"GO:0001798"}


id: PBO:0027356
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_nitrogen_starvation_gene_mRNA_during_vegetative_growth","termid":"PBO:0027356"}


id: GO:0061596
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction 2,3-dihydroxypropane-1-sulfonate + NAD+ = 3-sulfolactaldehyde + NADH + H+.","definition_xrefs":["PMID:24463506","EC:1.1.1.373","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"3-sulfolactaldehyde reductase activity","secondary_identifiers":["MetaCyc:RXN-15299","RHEA:40511"],"termid":"GO:0061596"}


id: GO:0050972
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events involved in echolocation in which a mechanical stimulus is received and converted into a molecular signal. The stimulus is in the form of a reflected sound wave (an echo), which the organism uses to determine the distance to the object that reflected the sound wave.","definition_xrefs":["GOC:ai","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of mechanical stimulus involved in sensory perception","termid":"GO:0050974"},{"relation_name":"part_of","term_name":"echolocation","termid":"GO:0050959"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of mechanical stimulus involved in echolocation","synonyms":[{"name":"echolocation, detection of mechanical stimulus","type":"exact"},{"name":"echolocation, sensory detection of mechanical stimulus","type":"exact"},{"name":"echolocation, sensory transduction of mechanical stimulus","type":"exact"},{"name":"sensory detection of mechanical stimulus during echolocation","type":"exact"},{"name":"sensory transduction of mechanical stimulus during echolocation","type":"exact"}],"termid":"GO:0050972"}


id: GO:0045049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process of protein insertion into the endoplasmic reticulum (ER) membrane in which N-terminal cleaved signal sequences direct polypeptides to the ER.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein insertion into ER membrane","termid":"GO:0045048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0061024","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein insertion into ER membrane by N-terminal cleaved signal sequence","synonyms":[{"name":"N-terminal cleaved signal sequence mediated protein insertion into ER membrane","type":"exact"},{"name":"protein insertion into ER membrane, N-terminal cleaved signal sequence mediated","type":"exact"},{"name":"protein insertion into endoplasmic reticulum membrane by N-terminal cleaved signal sequence","type":"exact"},{"name":"protein-ER insertion by N-terminal cleaved signal sequence","type":"exact"},{"name":"protein-endoplasmic reticulum insertion by N-terminal cleaved signal sequence","type":"exact"}],"termid":"GO:0045049"}


id: PBO:0109463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR9-2 host gene","termid":"PBO:0109463"}


id: MONDO:0859200
data:
  {"annotated_genes":["SJAG_04153"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86575],"is_not":false,"summary":null,"term":"MONDO:0859200"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04153":null},"genotype_count":0,"is_obsolete":false,"name":"cerebellar ataxia, brain abnormalities, and cardiac conduction defects","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:641361","MEDGEN:1794215","UMLS:C5562005","OMIM:619576"],"synonyms":[{"name":"neurodevelopmental delay-hypotonia-cerebellar ataxia-cardiac conduction defects syndrome","type":"exact"}],"termid":"MONDO:0859200","terms_by_termid":{"MONDO:0859200":null},"xrefs":{"Monarch":{"xref_id":"0859200"}}}


id: MONDO:0003566
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete choroid plexus carcinoma (obsolete MONDO:0003566)","termid":"MONDO:0003566","xrefs":{"Monarch":{"xref_id":"0003566"}}}


id: PBO:0082125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Acid trehalase required for utilization of extracellular trehalose; involved in intracellular trehalose degradation during growth recovery after saline stress","termid":"PBO:0082125"}


id: GO:0015577
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a galactitol from one side of a membrane to the other. Galactitol is the hexitol derived by the reduction of the aldehyde group of either D- or L-galactose.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transmembrane transporter activity","termid":"GO:0015144"},{"relation_name":"is_a","term_name":"polyol transmembrane transporter activity","termid":"GO:0015166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"galactitol transmembrane transporter activity","secondary_identifiers":["GO:0015588"],"synonyms":[{"name":"galactitol permease activity","type":"exact"}],"termid":"GO:0015577"}


id: FYPO:0000919
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of citrate (Si)-synthase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal citrate (Si)-synthase activity","termid":"FYPO:0000917"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000654","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"increased citrate (Si)-synthase activity","synonyms":[{"name":"increased citrate synthase activity","type":"broad"}],"termid":"FYPO:0000919"}


id: GO:0001958
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Replacement ossification wherein bone tissue replaces cartilage.","definition_xrefs":["ISBN:0878932437","GO_REF:0000034"],"direct_ancestors":[{"relation_name":"is_a","term_name":"replacement ossification","termid":"GO:0036075"},{"relation_name":"part_of","term_name":"endochondral bone morphogenesis","termid":"GO:0060350"}],"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":"endochondral ossification","secondary_identifiers":["Wikipedia:Endochondral_ossification"],"termid":"GO:0001958"}


id: GO:1900598
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of demethylkotanin.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolite catabolic process","termid":"GO:0090487"},{"relation_name":"is_a","term_name":"demethylkotanin metabolic process","termid":"GO:1900597"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"demethylkotanin catabolic process","synonyms":[{"name":"demethylkotanin breakdown","type":"exact"},{"name":"demethylkotanin catabolism","type":"exact"},{"name":"demethylkotanin degradation","type":"exact"}],"termid":"GO:1900598"}


id: PBO:0114346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane amino acid transmembrane transporter Isp5","termid":"PBO:0114346"}


id: PBO:0054704
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 2113","termid":"PBO:0054704"}


id: PBO:0002471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP-type peptidyl-prolyl cis-trans isomerase (predicted)","termid":"PBO:0002471"}


id: PBO:0060991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NHERF family PDZ scaffold protein 2","termid":"PBO:0060991"}


id: GO:0051398
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of a lysine residue from the N-terminal of an oligopeptide or polypeptide chain.","definition_xrefs":["PMID:12799365","GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal lysine aminopeptidase activity (obsolete GO:0051398)","synonyms":[{"name":"N-terminal lysine aminopeptidase activity","type":"exact"},{"name":"lysine aminopeptidase activity","type":"broad"},{"name":"lysyl aminopeptidase activity","type":"broad"}],"termid":"GO:0051398"}


id: PBO:0074698
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 70H","termid":"PBO:0074698"}


id: GO:1905621
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of alpha-(1->3)-fucosyltransferase activity.","definition_xrefs":["GOC:TermGenie","PMID:15364955","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of alpha-(1->3)-fucosyltransferase activity (obsolete GO:1905621)","synonyms":[{"name":"activation of alpha(1,3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-(1,3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-(1->3)-fucosyltransferase activity","type":"narrow"},{"name":"activation of alpha-1,3-fucosyltransferase activity","type":"narrow"},{"name":"positive regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"positive regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"positive regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"up regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"up-regulation of alpha-1,3-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha(1,3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-(1,3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-(1->3)-fucosyltransferase activity","type":"exact"},{"name":"upregulation of alpha-1,3-fucosyltransferase activity","type":"exact"}],"termid":"GO:1905621"}


id: PBO:0034729
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"although this is demonstrated to be a DNA polymerase epsilon interactor and named Dpb3, it appears to be the ortholog of S. cerevisiae BUR6 and human DRAP1. The Dpb3 ortholog appears to be the recently identified SPCC16C4.22","termid":"PBO:0034729"}


id: GO:0098794
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The part of a synapse that is part of the post-synaptic cell.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"synapse","termid":"GO:0045202"}],"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":"postsynapse","termid":"GO:0098794"}


id: MONDO:0021052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant, usually non-functioning, extra-adrenal paraganglioma that arises from paraganglia located along the parasympathetic nerves. Representative examples include aorticopulmonary, carotid body, jugulotympanic, and mediastinal paragangliomas.","definition_xrefs":["NCIT:C4217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paraganglioma","termid":"MONDO:0000448"},{"relation_name":"is_a","term_name":"parasympathetic nervous system disorder","termid":"MONDO:0044995"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parasympathetic paraganglioma","secondary_identifiers":["MEDGEN:90779","ICDO:8682/1","UMLS:C0334416"],"synonyms":[{"name":"paraganglioma of parasympathetic nervous system","type":"exact"},{"name":"parasympathetic Extra-adrenal paraganglioma","type":"exact"},{"name":"parasympathetic Paraganglionic neoplasm","type":"exact"},{"name":"parasympathetic nervous system paraganglioma","type":"exact"},{"name":"parasympathetic paraganglioma","type":"exact"}],"termid":"MONDO:0021052","xrefs":{"Monarch":{"xref_id":"0021052"}}}


id: PBO:0083475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene SKP1","termid":"PBO:0083475"}


id: PBO:0058442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5007","termid":"PBO:0058442"}


id: PBO:0054144
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 1511","termid":"PBO:0054144"}


id: GO:0070174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of enamel mineralization, the deposition of calcium salts in tooth enamel.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of tooth mineralization","termid":"GO:0070171"},{"relation_name":"is_a","term_name":"regulation of enamel mineralization","termid":"GO:0070173"},{"relation_name":"negatively_regulates","term_name":"enamel mineralization","termid":"GO:0070166"}],"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 enamel mineralization","termid":"GO:0070174"}


id: MONDO:0013851
data:
  {"annotated_genes":["SJAG_01840"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86632],"is_not":false,"summary":null,"term":"MONDO:0013851"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bone marrow failure syndrome","termid":"MONDO:0000159"},{"relation_name":"is_a","term_name":"inherited aplastic anemia","termid":"MONDO:0001713"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01840":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280","MONDO:0005046"],"is_obsolete":false,"name":"autosomal dominant aplasia and myelodysplasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3808553","MEDGEN:814883","OMIM:614675","GARD:17420","Orphanet:314399","NANDO:1200301"],"synonyms":[{"name":"BMFS1","type":"related"},{"name":"autosomal dominant aplastic anaemia and myelodysplasia","type":"exact"},{"name":"autosomal dominant aplastic anemia and myelodysplasia","type":"exact"},{"name":"bone marrow failure syndrome 1","type":"related"},{"name":"bone marrow failure syndrome type 1","type":"exact"}],"termid":"MONDO:0013851","terms_by_termid":{"MONDO:0013851":null},"xrefs":{"Monarch":{"xref_id":"0013851"}}}


id: FYPO:0005077
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a cell becomes elongated, i.e. has a greater length and length:diameter ratio than normal, when the cell is subject to glucose starvation.","definition_xrefs":["PMID:17179073","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated cell","termid":"FYPO:0000017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000005"],"is_obsolete":false,"name":"elongated cell during glucose starvation","synonyms":[{"name":"cell morphology, elongated cell during glucose starvation","type":"exact"},{"name":"elongated cell during glucose depletion","type":"exact"},{"name":"elongated cell during glucose deprivation","type":"exact"},{"name":"long cell during glucose starvation","type":"exact"}],"termid":"FYPO:0005077"}


id: GO:0010632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of epithelial cell migration.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"epithelial cell migration","termid":"GO:0010631"}],"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 epithelial cell migration","termid":"GO:0010632"}


id: MONDO:0001536
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the vagina. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C6373"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign vaginal neoplasm","termid":"MONDO:0000647"},{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vaginal leiomyoma","secondary_identifiers":["DOID:125","UMLS:C1336939","MEDGEN:277859"],"synonyms":[{"name":"leiomyoma of the vagina","type":"exact"},{"name":"leiomyoma of vagina","type":"exact"},{"name":"vagina leiomyoma","type":"exact"},{"name":"vaginal leiomyoma","type":"exact"}],"termid":"MONDO:0001536","xrefs":{"Monarch":{"xref_id":"0001536"}}}


id: PBO:0028174
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_double-strand_break_repair_during_vegetative_growth","termid":"PBO:0028174"}


id: GO:0050841
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The hydroxylation of peptidyl-N6,N6,N6-trimethyl-L-lysine to form peptidyl-N6,N6,N6-trimethyl-5-hydroxy-L-lysine.","definition_xrefs":["RESID:AA0359"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-N6,N6,N6-trimethyl-lysine hydroxylation to peptidyl-N6,N6,N6-trimethyl-5-hydroxy-L-lysine (obsolete GO:0050841)","synonyms":[{"name":"peptidyl trimethyl lysine hydroxylase activity","type":"exact"},{"name":"peptidyl-trimethyl-lysine hydroxylase activity","type":"exact"}],"termid":"GO:0050841"}


id: PBO:0043248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLDN7 pseudogene 1","termid":"PBO:0043248"}


id: PBO:0088678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-rRNA processing protein Esf1","termid":"PBO:0088678"}


id: PBO:0056883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MICOS10 pseudogene 3","termid":"PBO:0056883"}


id: GO:0106373
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-deoxyglucosone + H2O + NAD+ = 2-dehydro-3-deoxy-D-gluconate + 2 H+ + NADH.","definition_xrefs":["RHEA:67244","PMID:17175089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde dehydrogenase (NAD+) activity","termid":"GO:0004029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"3-deoxyglucosone dehydrogenase activity","termid":"GO:0106373"}


id: GO:0045300
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 H+ + O2 + octadecanoyl-[ACP] + 2 reduced [2Fe-2S]-[ferredoxin] = (9Z)-octadecenoyl-[ACP] + 2 H2O + 2 oxidized [2Fe-2S]-[ferredoxin].","definition_xrefs":["RHEA:11776"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water","termid":"GO:0016717"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"stearoyl-[ACP] desaturase activity","secondary_identifiers":["MetaCyc:RXN-7903","KEGG_REACTION:R03370","EC:1.14.19.2"],"synonyms":[{"name":"acyl-[acyl-carrier-protein] desaturase activity","type":"related"},{"name":"acyl-acyl-carrier-protein desaturase activity","type":"related"},{"name":"acyl-acyl-carrier-protein, hydrogen-donor:oxygen oxidoreductase activity","type":"related"},{"name":"stearyl acyl carrier protein desaturase activity","type":"related"},{"name":"stearyl-ACP desaturase activity","type":"related"}],"termid":"GO:0045300"}


id: MOD:00251
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-serine residue and the 5'-end of DNA through a phosphodiester bond to form O-(phospho-5'-DNA)-L-serine.","definition_xrefs":["PubMed:7142163","RESID:AA0246","PubMed:7265205"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyribonucleic acid linked residue","termid":"MOD:00750"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-(phospho-5'-DNA)-L-serine","synonyms":[{"name":"(S)-2-amino-3-(5'-deoxyribonucleic acid phosphonoxy)propanoic acid","type":"exact"},{"name":"ACT_SITE O-(5'-phospho-DNA)-serine intermediate","type":"exact"},{"name":"MOD_RES O-(5'-phospho-DNA)-serine","type":"exact"},{"name":"O-(phospho-5'-DNA)-L-serine","type":"exact"},{"name":"O3-(phospho-5'-DNA)-L-serine","type":"exact"},{"name":"O3-L-serine 5'-DNA phosphodiester","type":"exact"}],"termid":"MOD:00251"}


id: MONDO:0011280
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A schizophrenia that has material basis in an autosomal dominant mutation of SCZD6 on chromosome 8p21.","definition_xrefs":["DOID:0070082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"schizophrenia, susceptibility to","termid":"MONDO:0100182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schizophrenia 6","secondary_identifiers":["OMIM:603013","MEDGEN:350380","UMLS:C1864275"],"synonyms":[{"name":"SCZD6","type":"exact"},{"name":"schizophrenia 6","type":"exact"},{"name":"schizophrenia susceptibility locus, chromosome 8P-related","type":"exact"}],"termid":"MONDO:0011280","xrefs":{"Monarch":{"xref_id":"0011280"}}}


id: GO:1905514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of short-term synaptic potentiation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:15470145","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of biological process","termid":"GO:0048518"},{"relation_name":"is_a","term_name":"regulation of short-term synaptic potentiation","termid":"GO:1905512"},{"relation_name":"positively_regulates","term_name":"short-term synaptic potentiation","termid":"GO:1990926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of short-term synaptic potentiation","synonyms":[{"name":"activation of short-term synaptic potentiation","type":"narrow"},{"name":"activation of synaptic facilitation","type":"narrow"},{"name":"positive regulation of synaptic facilitation","type":"exact"},{"name":"up regulation of short-term synaptic potentiation","type":"exact"},{"name":"up regulation of synaptic facilitation","type":"exact"},{"name":"up-regulation of short-term synaptic potentiation","type":"exact"},{"name":"up-regulation of synaptic facilitation","type":"exact"},{"name":"upregulation of short-term synaptic potentiation","type":"exact"},{"name":"upregulation of synaptic facilitation","type":"exact"}],"termid":"GO:1905514"}


id: MONDO:0014492
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Woolly hair-palmoplantar keratoderma syndrome is a very rare, hereditary epidermal disorder characterized by hypotrichosis/wooly scalp hair, sparse body hair, eyelashes and eyebrows, leukonychia, and striate palmoplantar keratoderma (more severe on the soles than the palms), which progressively worsens with age. Pseudo ainhum of the fifth toes was also reported. Although wooly hair-palmoplantar keratoderma syndrome shares clinical similarities with both Naxos disease and Carvajal syndrome, cardiomyopathy is notably absent.","definition_xrefs":["Orphanet:420686"],"direct_ancestors":[{"relation_name":"is_a","term_name":"focal palmoplantar keratoderma","termid":"MONDO:0017672"}],"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":"wooly hair-palmoplantar keratoderma syndrome","secondary_identifiers":["MEDGEN:863639","DOID:0070554","GARD:17697","OMIM:616099","SCTID:764108000","UMLS:C4015202"],"synonyms":[{"name":"KWWH type IV","type":"exact"},{"name":"PPKWH","type":"related"},{"name":"keratoderma with woolly hair type IV","type":"exact"},{"name":"keratoderma with wooly hair type IV","type":"exact"},{"name":"palmoplantar keratoderma and woolly hair","type":"related"},{"name":"palmoplantar keratoderma and wooly hair","type":"related"},{"name":"woolly hair-palmoplantar hyperkeratosis syndrome","type":"exact"},{"name":"wooly hair-palmoplantar hyperkeratosis syndrome","type":"exact"}],"termid":"MONDO:0014492","xrefs":{"Monarch":{"xref_id":"0014492"}}}


id: MONDO:0013683
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial vesicoureteral reflux","termid":"MONDO:0017329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicoureteral reflux 5","secondary_identifiers":["GARD:18422","OMIM:614318","MEDGEN:482070","UMLS:C3280440"],"synonyms":[{"name":"VUR5","type":"exact"},{"name":"vesicoureteral reflux 5","type":"exact"}],"termid":"MONDO:0013683","xrefs":{"Monarch":{"xref_id":"0013683"}}}


id: MONDO:0032913
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital heart defects, multiple types, 7","secondary_identifiers":["OMIM:618780","UMLS:C5394062","MEDGEN:1714491"],"synonyms":[{"name":"CHTD7","type":"related"},{"name":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 7","type":"related"}],"termid":"MONDO:0032913","xrefs":{"Monarch":{"xref_id":"0032913"}}}


id: MONDO:0003707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from the common bile duct distal to the insertion of the cystic duct.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrahepatic bile duct carcinoma","termid":"MONDO:0003090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515","MONDO:0004992"],"is_obsolete":false,"name":"distal biliary tract carcinoma","secondary_identifiers":["NCIT:C7109","UMLS:C1333308","MEDGEN:232133","DOID:5923"],"synonyms":[{"name":"carcinoma of distal biliary tract","type":"exact"},{"name":"carcinoma of the distal biliary tract","type":"exact"},{"name":"distal bile duct cancer","type":"exact"},{"name":"distal bile duct carcinoma","type":"exact"},{"name":"distal biliary tract carcinoma","type":"exact"},{"name":"extrahepatic (distal) bile duct cancer","type":"exact"}],"termid":"MONDO:0003707","xrefs":{"Monarch":{"xref_id":"0003707"}}}


id: GO:0140774
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N6-octadecanoyl-L-lysyl-[protein] + NAD+ + H2O = octadecanoyl-ADP-D-ribose + L-lysyl-[protein] + nicotinamide.","definition_xrefs":["RHEA:70563","PMID:23552949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"NAD-dependent protein depalmitoylase activity","termid":"GO:0140774"}


id: PBO:0051695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INO80 complex subunit D","termid":"PBO:0051695"}


id: PBO:0117244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial peptidyl tRNA hydrolase, stalled-ribosome rescue factor srRF1, Pth4","termid":"PBO:0117244"}


id: PBO:0057346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 541","termid":"PBO:0057346"}


id: PBO:0072865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAM and SH3 domain containing 3","termid":"PBO:0072865"}


id: MONDO:0007920
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A frequent form of late-onset, primary lymphedema characterized by lower limb lymphedema typically developing during puberty.","definition_xrefs":["Orphanet:90186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"craniofacial dystonia","termid":"MONDO:0000486"},{"relation_name":"is_a","term_name":"lymphatic malformation","termid":"MONDO:0019313"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"},{"relation_name":"is_a","term_name":"inherited dystonia","termid":"MONDO:0044807"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0003441"],"is_obsolete":false,"name":"lymphatic malformation 5","secondary_identifiers":["SCTID:230325003","GARD:3324","MESH:C562467","SCTID:400040008","DOID:0070213","MedDRA:10027138","UMLS:C4746631","MEDGEN:1648463","OMIM:153200"],"synonyms":[{"name":"LMPH2","type":"exact"},{"name":"Meige disease","type":"exact"},{"name":"Meige lymphedema","type":"exact"},{"name":"hereditary lymphedema type II","type":"exact"},{"name":"late-onset lymphedema","type":"exact"},{"name":"late-onset primary lymphedema","type":"exact"},{"name":"lymphedema hereditary type 2","type":"related"},{"name":"lymphedema praecox","type":"related"},{"name":"lymphedema preacox","type":"exact"},{"name":"lymphedema, hereditary, II","type":"related"},{"name":"lymphedema, late-onset","type":"related"}],"termid":"MONDO:0007920","xrefs":{"Monarch":{"xref_id":"0007920"}}}


id: PBO:0072154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 31","termid":"PBO:0072154"}


id: PBO:0074944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 109A","termid":"PBO:0074944"}


id: PR:B5BP48
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An alpha-ketoglutarate-dependent taurine dioxygenase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00004"],"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-ketoglutarate-dependent sulfonate dioxygenase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC460.04c","secondary_identifiers":["UniProtKB:B5BP48"],"synonyms":[{"name":"Spom972h-tauD","type":"exact"}],"termid":"PR:B5BP48"}


id: GO:1900218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of apoptotic process involved in metanephric nephron tubule development.","definition_xrefs":["GOC:yaf","GOC:TermGenie","PMID:17314325","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process involved in metanephric nephron tubule development","termid":"GO:1900217"},{"relation_name":"is_a","term_name":"negative regulation of apoptotic process involved in development","termid":"GO:1904746"},{"relation_name":"negatively_regulates","term_name":"apoptotic process involved in metanephric nephron tubule development","termid":"GO:1900205"}],"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 apoptotic process involved in metanephric nephron tubule development","synonyms":[{"name":"down regulation of apoptosis of metanephric nephron tubule development","type":"narrow"},{"name":"down regulation of apoptotic cell death of metanephric nephron tubule development","type":"exact"},{"name":"down regulation of apoptotic process involved in metanephric nephron tubule development","type":"exact"},{"name":"down regulation of apoptotic process of metanephric nephron tubule development","type":"exact"},{"name":"down regulation of apoptotic program of metanephric nephron tubule development","type":"narrow"},{"name":"down regulation of apoptotic programmed cell death of metanephric nephron tubule development","type":"exact"},{"name":"down regulation of programmed cell death by apoptosis of metanephric nephron tubule development","type":"exact"},{"name":"down regulation of signaling (initiator) caspase activity of metanephric nephron tubule development","type":"related"},{"name":"down regulation of type I programmed cell death of metanephric nephron tubule development","type":"narrow"},{"name":"down-regulation of apoptosis of metanephric nephron tubule development","type":"narrow"},{"name":"down-regulation of apoptotic cell death of metanephric nephron tubule development","type":"exact"},{"name":"down-regulation of apoptotic process involved in metanephric nephron tubule development","type":"exact"},{"name":"down-regulation of apoptotic process of metanephric nephron tubule development","type":"exact"},{"name":"down-regulation of apoptotic program of metanephric nephron tubule development","type":"narrow"},{"name":"down-regulation of apoptotic programmed cell death of metanephric nephron tubule development","type":"exact"},{"name":"down-regulation of programmed cell death by apoptosis of metanephric nephron tubule development","type":"exact"},{"name":"down-regulation of signaling (initiator) caspase activity of metanephric nephron tubule development","type":"related"},{"name":"down-regulation of type I programmed cell death of metanephric nephron tubule development","type":"narrow"},{"name":"downregulation of apoptosis of metanephric nephron tubule development","type":"narrow"},{"name":"downregulation of apoptotic cell death of metanephric nephron tubule development","type":"exact"},{"name":"downregulation of apoptotic process involved in metanephric nephron tubule development","type":"exact"},{"name":"downregulation of apoptotic process of metanephric nephron tubule development","type":"exact"},{"name":"downregulation of apoptotic program of metanephric nephron tubule development","type":"narrow"},{"name":"downregulation of apoptotic programmed cell death of metanephric nephron tubule development","type":"exact"},{"name":"downregulation of programmed cell death by apoptosis of metanephric nephron tubule development","type":"exact"},{"name":"downregulation of signaling (initiator) caspase activity of metanephric nephron tubule development","type":"related"},{"name":"downregulation of type I programmed cell death of metanephric nephron tubule development","type":"narrow"},{"name":"inhibition of apoptosis of metanephric nephron tubule development","type":"narrow"},{"name":"inhibition of apoptotic cell death of metanephric nephron tubule development","type":"exact"},{"name":"inhibition of apoptotic process involved in metanephric nephron tubule development","type":"narrow"},{"name":"inhibition of apoptotic process of metanephric nephron tubule development","type":"exact"},{"name":"inhibition of apoptotic program of metanephric nephron tubule development","type":"narrow"},{"name":"inhibition of apoptotic programmed cell death of metanephric nephron tubule development","type":"exact"},{"name":"inhibition of programmed cell death by apoptosis of metanephric nephron tubule development","type":"exact"},{"name":"inhibition of signaling (initiator) caspase activity of metanephric nephron tubule development","type":"related"},{"name":"inhibition of type I programmed cell death of metanephric nephron tubule development","type":"narrow"},{"name":"negative regulation of apoptosis of metanephric nephron tubule development","type":"narrow"},{"name":"negative regulation of apoptotic cell death of metanephric nephron tubule development","type":"exact"},{"name":"negative regulation of apoptotic process of metanephric nephron tubule development","type":"exact"},{"name":"negative regulation of apoptotic program of metanephric nephron tubule development","type":"narrow"},{"name":"negative regulation of apoptotic programmed cell death of metanephric nephron tubule development","type":"exact"},{"name":"negative regulation of programmed cell death by apoptosis of metanephric nephron tubule development","type":"exact"},{"name":"negative regulation of signaling (initiator) caspase activity of metanephric nephron tubule development","type":"related"},{"name":"negative regulation of type I programmed cell death of metanephric nephron tubule development","type":"narrow"}],"termid":"GO:1900218"}


id: MONDO:0008185
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary chronic pancreatitis (HCP), a rare inherited form of pancreatitis is defined as recurrent acute pancreatitis and/or chronic pancreatitis in two first-degree relatives or 3 or more second-degree relatives in 2 or more generations, for which no predisposing factors are identified. HCP is characterized by irreversible damage to both exocrine and endocrine components of the pancreas.","definition_xrefs":["Orphanet:676"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"chronic pancreatitis","termid":"MONDO:0005003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"hereditary chronic pancreatitis","secondary_identifiers":["GARD:6632","MESH:C537262","UMLS:C0238339","icd11.foundation:1287702961","OMIM:167800","NANDO:2200942","ICD9:577.8","MEDGEN:116056","NCIT:C95436","SCTID:68072000","NANDO:1200921"],"synonyms":[{"name":"HPC","type":"related"},{"name":"Hp","type":"related"},{"name":"PCTT","type":"related"},{"name":"autosomal dominant hereditary pancreatitis","type":"related"},{"name":"familial pancreatitis","type":"related"},{"name":"hereditary chronic pancreatitis","type":"exact"},{"name":"hereditary pancreatitis","type":"exact"},{"name":"pancreatitis, calcific","type":"related"},{"name":"pancreatitis, calcific, included","type":"related"},{"name":"pancreatitis, chronic","type":"related"},{"name":"pancreatitis, chronic pancreatitis, chronic, susceptibility to, included","type":"related"},{"name":"pancreatitis, chronic, protection against","type":"related"},{"name":"pancreatitis, chronic, protection against, included","type":"related"},{"name":"pancreatitis, chronic, susceptibility to","type":"related"},{"name":"pancreatitis, hereditary","type":"related"}],"termid":"MONDO:0008185","xrefs":{"Monarch":{"xref_id":"0008185"}}}


id: MONDO:0004310
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An embryonal tumor with multilayered rosettes, C19MC-altered, occurring in adults.","definition_xrefs":["NCIT:C8290"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult central nervous system primitive neuroectodermal neoplasm","termid":"MONDO:0002795"},{"relation_name":"is_a","term_name":"ependymoblastoma","termid":"MONDO:0016715"}],"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":"adult embryonal tumor with multilayered rosettes, c19mc-altered","secondary_identifiers":["UMLS:C0281330","DOID:7631","MEDGEN:83792"],"synonyms":[{"name":"adult embryonal tumor with multilayered rosettes, C19MC-altered","type":"exact"},{"name":"adult embryonal tumour with multilayered rosettes, C19MC-altered","type":"exact"},{"name":"adult ependymoblastoma","type":"exact"},{"name":"embryonal tumor with multilayered rosettes, C19MC-altered","type":"broad"},{"name":"embryonal tumour with multilayered rosettes, C19MC-altered","type":"broad"},{"name":"ependymoblastoma of adults","type":"exact"}],"termid":"MONDO:0004310","xrefs":{"Monarch":{"xref_id":"0004310"}}}


id: GO:0021525
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which differentiating motor neurons in the neural tube acquire the specialized structural and/or functional features of lateral motor column neurons. Lateral motor column neurons are generated only on limb levels and send axons into the limb mesenchyme. Differentiation includes the processes involved in commitment of a cell to a specific fate.","definition_xrefs":["GO_REF:0000021","GOC:jid","GOC:cls","GOC:dgh","GOC:dph","PMID:11262869"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spinal cord motor neuron differentiation","termid":"GO:0021522"},{"relation_name":"part_of","term_name":"somatic motor neuron differentiation","termid":"GO:0021523"}],"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 motor column neuron differentiation","termid":"GO:0021525"}


id: GO:0009049
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage of a signal peptide from a protein precursor by an aspartic endopeptidase mechanism.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete aspartic-type signal peptidase activity (obsolete GO:0009049)","synonyms":[{"name":"aspartic-type signal peptidase activity","type":"exact"}],"termid":"GO:0009049"}


id: MONDO:0030293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary angioedema","termid":"MONDO:0019623"}],"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":"angioedema, hereditary, 5","secondary_identifiers":["MEDGEN:1780904","OMIM:619361","UMLS:C5543508"],"synonyms":[{"name":"HAE5","type":"exact"},{"name":"angioedema, hereditary, 5","type":"exact"}],"termid":"MONDO:0030293","xrefs":{"Monarch":{"xref_id":"0030293"}}}


id: PBO:0067247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 320, pseudogene","termid":"PBO:0067247"}


id: PBO:0001323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arginine-tRNA protein transferase (predicted)","termid":"PBO:0001323"}


id: GO:0002448
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the carrying out of an immune response by a mast cell.","definition_xrefs":["ISBN:0781735149","GO_REF:0000022","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukocyte mediated immunity","termid":"GO:0002444"}],"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":"mast cell mediated immunity","termid":"GO:0002448"}


id: PATO:0002487
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a process by virtue of that process having exactly one organism as a participant.","definition_xrefs":["PATOC:DS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"process quality","termid":"PATO:0001236"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"single organismal process quality","termid":"PATO:0002487"}


id: PBO:0086895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative transporter; member of the sugar porter family","termid":"PBO:0086895"}


id: GO:0048208
data:
  {"annotated_genes":["SJAG_04615","SJAG_00906"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76526,71678],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0003400"}]},"cv_name":"biological_process","definition":"The addition of COPII proteins and adaptor proteins to ER membranes during the formation of transport vesicles, forming a vesicle coat.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ascb_2009","GOC:mah","ISBN:0716731363","GOC:jid","PMID:10219233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle coating","termid":"GO:0006901"},{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"vesicle targeting, rough ER to cis-Golgi","termid":"GO:0048207"},{"relation_name":"part_of","term_name":"COPII-coated vesicle budding","termid":"GO:0090114"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00906":null,"SJAG_04615":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0065003","GO:0008150","GO:0061024","GO:0016192","GO:0044085"],"is_obsolete":false,"name":"COPII vesicle coating","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-204005"],"synonyms":[{"name":"COPII coating of ER-derived vesicle","type":"exact"},{"name":"COPII vesicle coat assembly","type":"exact"},{"name":"COPII vesicle coat formation","type":"exact"}],"termid":"GO:0048208","terms_by_termid":{"GO:0003400":null}}


id: PBO:0058694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6822","termid":"PBO:0058694"}


id: FYPO:0005547
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 protein targeting to the vacuole occurs to a lower extent than normal, and some of the protein is secreted.","definition_xrefs":["PMID:22484924","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein targeting to vacuole","termid":"FYPO:0000676"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein targeting to vacuole, with protein secreted","synonyms":[{"name":"decreased protein targeting to vacuole, with protein secreted, during mitotic cell cycle","type":"related"},{"name":"decreased protein targeting to vacuole, with protein secreted, during vegetative growth","type":"exact"},{"name":"protein partially mislocalized from vacuole to extracellular region","type":"related"},{"name":"reduced protein targeting to vacuole, with protein secreted","type":"exact"}],"termid":"FYPO:0005547"}


id: GO:0071499
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 laminar fluid shear stress stimulus. Laminar fluid flow is the force acting on an object in a system where the fluid is moving across a solid surface in parallel layers.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to laminar fluid shear stress","termid":"GO:0034616"},{"relation_name":"is_a","term_name":"cellular response to fluid shear stress","termid":"GO:0071498"}],"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 laminar fluid shear stress","termid":"GO:0071499"}


id: PBO:0064880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 catalytic subunit alpha","termid":"PBO:0064880"}


id: GO:0046974
data:
  {"annotated_genes":["SJAG_04574"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110821],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140948"},{"annotations":[63068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140949"},{"annotations":[110823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140947"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + histone H3 L-lysine (position 9) = S-adenosyl-L-homocysteine + histone H3 N6-methyl-L-lysine (position 9). This reaction is the addition of up to three methyl groups to the lysine residue at position 9 of the histone H3 protein.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-lysine N-methyltransferase activity","termid":"GO:0016279"},{"relation_name":"is_a","term_name":"histone H3 methyltransferase activity","termid":"GO:0140938"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04574":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0140096","GO:0016741","GO:0008276","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"histone H3K9 methyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-427527","Reactome:R-HSA-427336"],"synonyms":[{"name":"histone H3K9 methylase activity","type":"exact"},{"name":"histone lysine N-methyltransferase activity (H3-K9 specific)","type":"exact"},{"name":"histone methylase activity (H3-K9 specific)","type":"exact"},{"name":"histone methyltransferase activity (H3-K9 specific)","type":"exact"},{"name":"histone-H3K9 methyltransferase activity","type":"exact"}],"termid":"GO:0046974","terms_by_termid":{"GO:0140947":null,"GO:0140948":null,"GO:0140949":null}}


id: PBO:0024480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PITH domain-containing protein","termid":"PBO:0024480"}


id: PBO:0002823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor Hsf1","termid":"PBO:0002823"}


id: PBO:0074130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 31 member 2","termid":"PBO:0074130"}


id: MONDO:0007502
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ear pits, posterior helical","secondary_identifiers":["OMIM:128710","UMLS:C1851900","MEDGEN:342119"],"synonyms":[{"name":"ear pits, posterior helical","type":"exact"},{"name":"earlobe Indentations, posterior","type":"related"},{"name":"posterior helical Ear pits","type":"related"}],"termid":"MONDO:0007502","xrefs":{"Monarch":{"xref_id":"0007502"}}}


id: PBO:0109145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRUNE1 pseudogene 1","termid":"PBO:0109145"}


id: GO:0035581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of binding or confining an extracellular signaling ligand, such that the ligand is unable to bind to its cell surface receptor.","definition_xrefs":["GOC:signaling","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular negative regulation of signal transduction","termid":"GO:1900116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"sequestering of extracellular ligand from receptor","synonyms":[{"name":"extracellular sequestering of receptor ligand","type":"exact"},{"name":"negative regulation of protein bioavailability","type":"related"}],"termid":"GO:0035581"}


id: PBO:0068042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 347","termid":"PBO:0068042"}


id: PBO:0001627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE Tlg2 (predicted)","termid":"PBO:0001627"}


id: PBO:0036279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic protein, human CCDC82 ortholog","termid":"PBO:0036279"}


id: GO:0044074
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a symbiont organism stops, prevents, or reduces the frequency, rate or extent of translation, the chemical reactions and pathways resulting in the formation of a protein, in its host organism.","definition_xrefs":["MITRE:tk"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by symbiont of host translation (obsolete GO:0044074)","synonyms":[{"name":"negative regulation of host translation by symbiont","type":"exact"}],"termid":"GO:0044074"}


id: GO:0008371
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. These are terms that have been removed from the active process ontology.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete biological process (obsolete GO:0008371)","termid":"GO:0008371"}


id: GO:0006205
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete pyrimidine metabolic process (obsolete GO:0006205)","synonyms":[{"name":"pyrimidine metabolic process","type":"exact"}],"termid":"GO:0006205"}


id: PBO:0067411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 521, pseudogene","termid":"PBO:0067411"}


id: MONDO:0100298
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abdominal wall malformation","termid":"MONDO:0100298","xrefs":{"Monarch":{"xref_id":"0100298"}}}


id: PBO:0002706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin depolymerizing factor, cofilin","termid":"PBO:0002706"}


id: GO:0062066
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a PSII associated light-harvesting complex II.","definition_xrefs":["PMID:17400553"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"PSII associated light-harvesting complex II binding","termid":"GO:0062066"}


id: PBO:0080291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 55 pseudogene","termid":"PBO:0080291"}


id: PBO:0012017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"simialar to S. pombe SPAC1F8.07c (paralog)","termid":"PBO:0012017"}


id: MONDO:0019846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acquired central diabetes insipidus (acquired CDI) is a subtype of central diabetes insipidus (CDI), characterized by polyuria and polydipsia, due to an idiopathic or secondary decrease in vasopressin (AVP) production.","definition_xrefs":["Orphanet:95626"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central diabetes insipidus","termid":"MONDO:0015790"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acquired central diabetes insipidus","secondary_identifiers":["MEDGEN:1843437","icd11.foundation:1677009817","GARD:19291","ICD10CM:E23.2","UMLS:C5680256"],"synonyms":[{"name":"acquired CDI","type":"exact"},{"name":"acquired central diabetes insipidus","type":"exact"},{"name":"acquired neurogenic diabetes insipidus","type":"exact"}],"termid":"MONDO:0019846","xrefs":{"Monarch":{"xref_id":"0019846"}}}


id: GO:2001283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any Roundabout signaling pathway that is involved in the directed movement of a muscle cell towards a tendon cell in response to an external stimulus.","definition_xrefs":["GOC:obol","GOC:bf","GOC:sart","PMID:19793885"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Roundabout signaling pathway","termid":"GO:0035385"},{"relation_name":"part_of","term_name":"muscle cell chemotaxis toward tendon cell","termid":"GO:0036061"}],"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":"Roundabout signaling pathway involved in muscle cell chemotaxis toward tendon cell","synonyms":[{"name":"ROBO signaling pathway involved in muscle cell attraction","type":"related"},{"name":"ROBO signaling pathway involved in muscle cell chemotaxis toward tendon cell","type":"exact"},{"name":"ROBO signaling pathway involved in muscle cell chemotaxis towards tendon cell","type":"exact"},{"name":"ROBO/SLIT signaling pathway involved in muscle cell attraction","type":"related"},{"name":"ROBO/SLIT signaling pathway involved in muscle cell chemotaxis toward tendon cell","type":"exact"},{"name":"ROBO/SLIT signaling pathway involved in muscle cell chemotaxis towards tendon cell","type":"exact"},{"name":"Roundabout signaling pathway involved in muscle cell attraction","type":"related"},{"name":"Roundabout signaling pathway involved in muscle cell chemotaxis towards tendon cell","type":"exact"},{"name":"Roundabout signalling pathway involved in muscle cell attraction","type":"related"},{"name":"Roundabout signalling pathway involved in muscle cell chemotaxis toward tendon cell","type":"exact"},{"name":"Roundabout signalling pathway involved in muscle cell chemotaxis towards tendon cell","type":"exact"}],"termid":"GO:2001283"}


id: PBO:0062355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily P member 1","termid":"PBO:0062355"}


id: PBO:0064571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"popeye domain containing 3","termid":"PBO:0064571"}


id: PBO:0058556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6165","termid":"PBO:0058556"}


id: GO:0032359
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The molecular events that lead to the excision of a viral genome from the host genome.","definition_xrefs":["VZ:3969","GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"release from viral latency","termid":"GO:0019046"}],"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":"provirus excision","synonyms":[{"name":"prophage excision","type":"exact"}],"termid":"GO:0032359"}


id: GO:0009678
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: diphosphate + H+(in) + H2O = 2 H+(out) + 2 phosphate.","definition_xrefs":["Wikipedia:Proton-pumping_pyrophosphatase","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton transmembrane transporter activity","termid":"GO:0015078"},{"relation_name":"is_a","term_name":"active monoatomic ion transmembrane transporter activity","termid":"GO:0022853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"diphosphate hydrolysis-driven proton transmembrane transporter activity","secondary_identifiers":["EC:7.1.3.1","TC:3.A.10","RHEA:13973","MetaCyc:TRANS-RXN-370"],"synonyms":[{"name":"H+-exporting diphosphatase","type":"related"},{"name":"PP(i) hydrolysis-driven proton transmembrane transporter activity","type":"exact"},{"name":"hydrogen-translocating pyrophosphatase activity","type":"related"},{"name":"proton-pumping diphosphatase","type":"related"},{"name":"proton-pumping pyrophosphatase","type":"related"},{"name":"proton-translocating pyrophosphatase activity","type":"exact"},{"name":"pyrophosphate hydrolysis-driven proton transmembrane transporter activity","type":"related"}],"termid":"GO:0009678"}


id: PBO:0026657
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-heterochromatin_assembly_beyond_boundary_element_IRC1L","termid":"PBO:0026657"}


id: GO:0098950
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic early endosome membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:mah","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of postsynaptic early endosome membrane (obsolete GO:0098950)","synonyms":[{"name":"intrinsic to postsynaptic early endosome membrane","type":"narrow"}],"termid":"GO:0098950"}


id: PBO:0027488
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_level_during_G0","termid":"PBO:0027488"}


id: PBO:0069006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 250, pseudogene","termid":"PBO:0069006"}


id: PBO:0074337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2","termid":"PBO:0074337"}


id: MONDO:0015295
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intractable diarrhea-choanal atresia-eye anomalies syndrome is characterized by the association of intractable diarrhea of infancy with choanal atresia. Short stature, a prominent and broad nasal bridge, micrognathia, single palmar creases, chronic corneal inflammation, cytopenia, and abnormal hair texture were also reported. So far, the syndrome has been described in three children from the same family. The absence of intellectual deficit and immune deficiency allow this syndrome to be distinguished from other forms of intractable diarrhea of infancy described previously.","definition_xrefs":["Orphanet:137622"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"intractable diarrhea-choanal atresia-eye anomalies syndrome","secondary_identifiers":["MEDGEN:929976","UMLS:C4304307","GARD:19882"],"termid":"MONDO:0015295","xrefs":{"Monarch":{"xref_id":"0015295"}}}


id: MONDO:0017736
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease","termid":"MONDO:0002561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561"],"is_obsolete":false,"name":"disorder of sialic acid metabolism","secondary_identifiers":["GARD:21332","SCTID:238050009","UMLS:C0342851","icd11.foundation:1709765980","MEDGEN:575253","ICD9:277.89","Orphanet:309319"],"termid":"MONDO:0017736","xrefs":{"Monarch":{"xref_id":"0017736"}}}


id: MONDO:0001533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"enthesopathy","termid":"MONDO:0002183"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pes anserinus tendinitis or bursitis","secondary_identifiers":["MEDGEN:592819","UMLS:C0410086","DOID:12475","ICD9:726.61"],"termid":"MONDO:0001533","xrefs":{"Monarch":{"xref_id":"0001533"}}}


id: MONDO:0014739
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 MET 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:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 97","secondary_identifiers":["GARD:22655","OMIM:616705","DOID:0110539","MEDGEN:899875","UMLS:C4084709"],"synonyms":[{"name":"DFNB97","type":"narrow"},{"name":"MET autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 97","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 97","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in MET","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 97","type":"narrow"},{"name":"deafness, autosomal recessive 97","type":"narrow"},{"name":"deafness, autosomal recessive type 97","type":"narrow"}],"termid":"MONDO:0014739","xrefs":{"Monarch":{"xref_id":"0014739"}}}


id: GO:0006420
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of coupling arginine to arginyl-tRNA, catalyzed by arginyl-tRNA synthetase. The arginyl-tRNA synthetase is a class-I synthetase. The activated amino acid is transferred to the 2'-OH group of an alanine accetping tRNA. The 2'-O-aminoacyl-tRNA will ultimately migrate to the 3' position via transesterification.","definition_xrefs":["GOC:mcc","ISBN:0716730510"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA aminoacylation for protein translation","termid":"GO:0006418"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0008150","GO:0006399","GO:0006520","GO:0010467"],"is_obsolete":false,"name":"arginyl-tRNA aminoacylation","termid":"GO:0006420"}


id: GO:0052488
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by organism of pathogen-associated molecular pattern-induced symbiont innate immunity (obsolete GO:0052488)","synonyms":[{"name":"negative regulation by organism of pathogen-associated molecular pattern-induced symbiont innate immunity","type":"exact"},{"name":"suppression of MAMP induced symbiont innate immunity","type":"exact"},{"name":"suppression of MAMP-induced symbiont innate immunity","type":"exact"},{"name":"suppression of PAMP induced symbiont innate immunity","type":"exact"},{"name":"suppression of PAMP-induced symbiont innate immunity","type":"exact"},{"name":"suppression of general elicitor induced symbiont innate immunity","type":"exact"},{"name":"suppression of general elicitor-induced symbiont innate immunity","type":"exact"},{"name":"suppression of pathogen-associated molecular pattern-induced symbiont innate immunity","type":"exact"}],"termid":"GO:0052488"}


id: PBO:0076635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transducin beta like 2","termid":"PBO:0076635"}


id: MONDO:0014248
data:
  {"annotated_genes":["SJAG_04697"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86144],"is_not":false,"summary":null,"term":"MONDO:0014248"}]},"cv_name":"mondo","definition":"SLC35A3-CDG is a form of congenital disorders of N-linked glycosylation characterized by distal arthrogryposis (mild flexion contractures of the fingers, deviation of the distal phalanges, swan-neck deformity), retromicrognathia, general muscle hypotonia, delayed psychomotor development, autism spectrum disorder (speech delay, abnormal use of speech, difficulties in initiating, understanding and maintaining social interaction, limited non-verbal communication and repetitive behavior), seizures, microcephaly and mild to moderate intellectual disability that becomes apparent with age. The disease is caused by mutations in the gene SLC35A3 (1p21).","definition_xrefs":["Orphanet:370943"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"},{"relation_name":"is_a","term_name":"distal arthrogryposis","termid":"MONDO:0019942"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04697":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"autism spectrum disorder - epilepsy - arthrogryposis syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:816240","OMIM:615553","GARD:17604","UMLS:C3809910"],"synonyms":[{"name":"AMRS","type":"related"},{"name":"SLC35A3-CDG","type":"exact"},{"name":"arthrogryposis, impaired intellectual development, and seizures","type":"exact"},{"name":"arthrogryposis, intellectual disability, and seizures","type":"related"},{"name":"arthrogryposis, mental retardation, and seizures","type":"related"}],"termid":"MONDO:0014248","terms_by_termid":{"MONDO:0014248":null},"xrefs":{"Monarch":{"xref_id":"0014248"}}}


id: PBO:0089360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane PTR family peptide transmembrane transporter Ptr2","termid":"PBO:0089360"}


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


id: PBO:0108900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 13","termid":"PBO:0108900"}


id: GO:1990537
data:
  {"annotated_genes":["SJAG_01613","SJAG_01224","SJAG_00918","SJAG_02624"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[98937,99537,107819,118471],"is_not":false,"summary":null,"term":"GO:1990537"}]},"cv_name":"cellular_component","definition":"Any of the mitotic spindle microtubules that come from each pole and overlap at the spindle midzone.","definition_xrefs":["PMID:16079915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polar microtubule","termid":"GO:0005827"},{"relation_name":"is_a","term_name":"mitotic spindle microtubule","termid":"GO:1990498"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00918":null,"SJAG_01224":null,"SJAG_01613":null,"SJAG_02624":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"part_of","termid":"GO:0072686"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0015630","GO:0005575","GO:0072686"],"is_obsolete":false,"name":"mitotic spindle polar microtubule","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990537","terms_by_termid":{"GO:1990537":null}}


id: GO:0061016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of snRNA, small nuclear ribonucleic acid, to a Cajal body.","definition_xrefs":["GOC:ascb_2009","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA localization to Cajal body","termid":"GO:0090670"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"snRNA localization to Cajal body","termid":"GO:0061016"}


id: PBO:0069728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1009, pseudogene","termid":"PBO:0069728"}


id: GO:0060797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by an extracellular ligand binding to a transforming growth factor beta receptor on the surface of a target cell, which contributes to an unspecified cell adopting a mesoderm fate.","definition_xrefs":["GOC:sdb_2009","GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment (obsolete GO:0060797)","synonyms":[{"name":"transforming growth factor beta receptor signalling pathway involved in primary germ layer cell fate commitment","type":"exact"}],"termid":"GO:0060797"}


id: MONDO:0009544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"megalencephaly","termid":"MONDO:0016608"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macrocephaly/megalencephaly syndrome, autosomal recessive","secondary_identifiers":["MESH:C537453","OMIM:248000","MEDGEN:812742","UMLS:C3806412"],"synonyms":[{"name":"Fryns Dereymaeker Haegeman syndrome","type":"related"},{"name":"MGCPH","type":"related"},{"name":"intellectual disability, macrocephaly, short stature and craniofacial dysmorphism","type":"related"},{"name":"macrocephaly/megalencephaly syndrome, autosomal recessive","type":"exact"},{"name":"mental retardation, macrocephaly, short stature and craniofacial dysmorphism","type":"related"}],"termid":"MONDO:0009544","xrefs":{"Monarch":{"xref_id":"0009544"}}}


id: PBO:0087875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional regulator; facilitates elongation through factors that modify RNAP II; role in peroxide resistance involving Rad2p; role in nonhomologous end-joining (NHEJ) of ds breaks in plasmid DNA, but not chromosomal DNA; role in the hyperosmotic stress response through polymerase recruitment at RNAP II and RNAP III genes; negatively regulates sporulation; protein abundance increases in response to DNA replication stress; functionally complemented by human SUB1 (PC4)","termid":"PBO:0087875"}


id: PBO:0048033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibronectin type III and SPRY domain containing 1","termid":"PBO:0048033"}


id: PBO:0047549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblast growth factor 7 pseudogene 8","termid":"PBO:0047549"}


id: PBO:0056562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minichromosome maintenance 9 homologous recombination repair factor","termid":"PBO:0056562"}


id: GO:0036387
data:
  {"annotated_genes":["SJAG_02348","SJAG_03927","SJAG_01267","SJAG_01762","SJAG_01354","SJAG_02607","SJAG_02394","SJAG_00857","SJAG_02800","SJAG_04210","SJAG_00884","SJAG_05301","SJAG_03451","SJAG_02074","SJAG_04062"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[58436,74122,62810,113504,103637,108149,108367,111712,72017,61124,57158,61348,111970,110885,66299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005656"}]},"cv_name":"cellular_component","definition":"A protein-DNA complex that forms at the origin of replication during the initial step of DNA replication and allows the origin to become competent, or 'licensed', for replication.","definition_xrefs":["GOC:jh2","Wikipedia:Pre-replication_complex","GOC:bhm","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex","termid":"GO:0032993"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00857":null,"SJAG_00884":null,"SJAG_01267":null,"SJAG_01354":null,"SJAG_01762":null,"SJAG_02074":null,"SJAG_02348":null,"SJAG_02394":null,"SJAG_02607":null,"SJAG_02800":null,"SJAG_03451":null,"SJAG_03927":null,"SJAG_04062":null,"SJAG_04210":null,"SJAG_05301":null},"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":"pre-replicative complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"pre-RC","type":"exact"},{"name":"pre-replication complex","type":"exact"}],"termid":"GO:0036387","terms_by_termid":{"GO:0005656":null}}


id: PBO:0074939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 104","termid":"PBO:0074939"}


id: SO:0000374
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An RNA with catalytic activity.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"ribozymic","termid":"SO:0001186"},{"relation_name":"is_a","term_name":"enzymatic_RNA","termid":"SO:0000372"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribozyme","secondary_identifiers":["http://en.wikipedia.org/wiki/Ribozyme"],"synonyms":[{"name":"INSDC_feature:ncRNA","type":"broad"},{"name":"INSDC_qualifier:ribozyme","type":"exact"}],"termid":"SO:0000374"}


id: PBO:0092006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Serine (gcu), mitochondrial","termid":"PBO:0092006"}


id: GO:0010351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of lithium ion into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["PMID:17270011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metal ion transport","termid":"GO:0030001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"lithium ion transport","synonyms":[{"name":"lithium transport","type":"exact"}],"termid":"GO:0010351"}


id: MONDO:0023659
data:
  {"annotated_genes":["SJAG_00330"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86860],"is_not":false,"summary":null,"term":"MONDO:0023659"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00330":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy 96","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5543446","OMIM:619340","MEDGEN:1780167","DOID:0070377","GARD:16445"],"synonyms":[{"name":"DEE96","type":"exact"}],"termid":"MONDO:0023659","terms_by_termid":{"MONDO:0023659":null},"xrefs":{"Monarch":{"xref_id":"0023659"}}}


id: PBO:0080435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS51 pseudogene 19","termid":"PBO:0080435"}


id: MONDO:0013305
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the fourth decade of life with high frequency progressive hearing loss and has material basis in a 269-kb duplication of chromosome 9q21.11 involving the TJP2 and FAM189A2 genes.","definition_xrefs":["DOID:0110577","PMID:20602916"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 51","secondary_identifiers":["MEDGEN:463625","OMIM:613558","UMLS:C3160736","GARD:18133"],"synonyms":[{"name":"DFNA51","type":"narrow"},{"name":"autosomal dominant deafness 51","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 51","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 51","type":"narrow"},{"name":"chromosome 9Q21.11 Duplication syndrome","type":"narrow"},{"name":"chromosome 9q21.11 duplication syndrome","type":"exact"},{"name":"deafness, autosomal dominant 51","type":"narrow"},{"name":"deafness, autosomal dominant type 51","type":"narrow"}],"termid":"MONDO:0013305","xrefs":{"Monarch":{"xref_id":"0013305"}}}


id: GO:0140999
data:
  {"annotated_genes":["SJAG_00769"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58699],"is_not":false,"summary":null,"term":"GO:0140999"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-lysyl4-[histone H3] + 3 S-adenosyl-L-methionine = 2 H+ + N6,N6-trimethyl-L-lysyl4-[histone H3] + 3 S-adenosyl-L-homocysteine. This reaction is the successive addition of three methyl groups to the unmethylated lysine residue at position 4 of histone H3, producing histone H3K4me3.","definition_xrefs":["PMID:18375658","RHEA:60260"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3K4 methyltransferase activity","termid":"GO:0042800"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00769":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016741","GO:0003824","GO:0140096","GO:0008276","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"histone H3K4 trimethyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["EC:2.1.1.354"],"synonyms":[{"name":"histone H3-K4 trimethylation","type":"broad"},{"name":"histone H3K4 trimethylase activity","type":"exact"},{"name":"histone H3K4 trimethylation","type":"broad"},{"name":"histone lysine N-trimethyltransferase activity (H3-K4 specific)","type":"exact"}],"termid":"GO:0140999","terms_by_termid":{"GO:0140999":null}}


id: PBO:0042303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD14 molecule","termid":"PBO:0042303"}


id: FYECO:0000332
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which 2-deoxyglucose 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":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 2-DG","synonyms":[{"name":"2-deoxy-D-glucose added","type":"exact"},{"name":"2-deoxyglucose added","type":"exact"}],"termid":"FYECO:0000332"}


id: PBO:0051650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine monophosphate dehydrogenase 1 pseudogene 5","termid":"PBO:0051650"}


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":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001985","FYPO:0001320","FYPO:0000004","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"}


