# terms

id: MOD:00411
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label. OBSOLETE because Unimod:18 is now merged with entry 258 remap to MOD:00581 'single 018 label'","definition_xrefs":["PubMed:18688235"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:00411 O18 label (obsolete MOD:00411)","termid":"MOD:00411"}


id: GO:0031633
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A chromatophore containing yellow pigment.","definition_xrefs":["ISBN:0395825172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane-derived chromatophore","termid":"GO:0042716"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"xanthophore","termid":"GO:0031633"}


id: GO:1990855
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of myo-inositol from outside of a cell into the intracellular region of a cell across the plasma membrane.","definition_xrefs":["PMID:9560432"],"gene_count":0,"genotype_count":0,"name":"obsolete myo-inositol import across plasma membrane (obsolete GO:1990855)","termid":"GO:1990855"}


id: PBO:0078322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor delta joining 4","termid":"PBO:0078322"}


id: MONDO:0002013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign lesion composed of dilated lymphatic channels. Painless swelling is the usual clinical manifestation.","definition_xrefs":["NCIT:C8965"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular organ benign neoplasm","termid":"MONDO:0000629"},{"relation_name":"is_a","term_name":"lymphatic vessel neoplasm","termid":"MONDO:0036870"}],"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":"lymphangioma","secondary_identifiers":["DOID:1475","UMLS:C0024221","MEDGEN:6153","SCTID:254836000","ICDO:9170/0","MESH:D008202","GARD:9789","NANDO:2201032","Orphanet:2415","SCTID:400178008","ICD9:228.1"],"synonyms":[{"name":"LM","type":"related"},{"name":"benign lymphangioma","type":"exact"},{"name":"benign lymphangioma (morphologic abnormality)","type":"exact"},{"name":"congenital lymphangioma","type":"narrow"},{"name":"lymphangioma","type":"exact"},{"name":"lymphangioma, benign","type":"exact"}],"termid":"MONDO:0002013","xrefs":{"Monarch":{"xref_id":"0002013"}}}


id: GO:2001312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a lysobisphosphatidic acid. A lysobisphosphatidic acid is a lysophosphatidic acid having the unusual property of a phosphodiester moiety linked to positions sn-1 and sn1' of glycerol; and two additional fatty acids esterified to the glycerol head group.","definition_xrefs":["GOC:mw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerophospholipid biosynthetic process","termid":"GO:0046474"},{"relation_name":"is_a","term_name":"carbohydrate derivative biosynthetic process","termid":"GO:1901137"},{"relation_name":"is_a","term_name":"lysobisphosphatidic acid metabolic process","termid":"GO:2001311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"lysobisphosphatidic acid biosynthetic process","secondary_identifiers":["Reactome:R-HSA-1483171"],"synonyms":[{"name":"LBPA anabolism","type":"exact"},{"name":"LBPA biosynthesis","type":"exact"},{"name":"LBPA biosynthetic process","type":"exact"},{"name":"LBPA formation","type":"exact"},{"name":"LBPA synthesis","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate (BMP) anabolism","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate (BMP) biosynthesis","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate (BMP) biosynthetic process","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate (BMP) formation","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate (BMP) synthesis","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate anabolism","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate biosynthesis","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate biosynthetic process","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate formation","type":"exact"},{"name":"bis(monoacylglycerol) hydrogen phosphate synthesis","type":"exact"},{"name":"lysobisphosphatidic acid anabolism","type":"exact"},{"name":"lysobisphosphatidic acid biosynthesis","type":"exact"},{"name":"lysobisphosphatidic acid formation","type":"exact"},{"name":"lysobisphosphatidic acid synthesis","type":"exact"}],"termid":"GO:2001312"}


id: PR:P30290
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mik1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P30290"],"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":"mitosis inhibitor protein kinase mik1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC660.14","synonyms":[{"name":"Spom972h-mik1","type":"exact"}],"termid":"PR:P30290"}


id: RO:0002455
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"mutualistically_interacts_with","termid":"RO:0002442"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pollinates","termid":"RO:0002455"}


id: PBO:0044137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTBP2 pseudogene 3","termid":"PBO:0044137"}


id: PBO:0084377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Long chain fatty acyl-CoA synthetase; activates imported fatty acids with a preference for C16:0-C18:0 chain lengths; green fluorescent protein (GFP)-fusion protein localizes to the cell periphery","termid":"PBO:0084377"}


id: MONDO:0021017
data:
  {"annotated_genes":["SJAG_00924","SJAG_01872","SJAG_03056","SJAG_04821","SJAG_00826","SJAG_04728"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012518"},{"annotations":[87909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013883"},{"annotations":[87146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014543"},{"annotations":[87143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014542"},{"annotations":[86986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014590"},{"annotations":[87776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012157"},{"annotations":[88018],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032596"}]},"cv_name":"mondo","definition":"A disease caused by dysfunction of synapses.","definition_xrefs":["Wikipedia:Synaptopathy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00826":null,"SJAG_00924":null,"SJAG_01872":null,"SJAG_03056":null,"SJAG_04728":null,"SJAG_04821":null},"genotype_count":0,"is_obsolete":false,"name":"synaptopathy","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0021017","terms_by_termid":{"MONDO:0012157":null,"MONDO:0012518":null,"MONDO:0013883":null,"MONDO:0014542":null,"MONDO:0014543":null,"MONDO:0014590":null,"MONDO:0032596":null},"xrefs":{"Monarch":{"xref_id":"0021017"}}}


id: GO:0047428
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 H2O + 4-chlorophenylacetonitrile = 4-chlorophenylacetate + NH3.","definition_xrefs":["EC:3.5.5.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrilase activity","termid":"GO:0000257"}],"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:0016810"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0016810","GO:0003674"],"is_obsolete":false,"name":"arylacetonitrilase activity","secondary_identifiers":["MetaCyc:3.5.5.5-RXN","RHEA:20657"],"synonyms":[{"name":"arylacetonitrile aminohydrolase activity","type":"related"}],"termid":"GO:0047428"}


id: MONDO:0015970
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic parathyroid disease and phosphocalcic metabolism disorder (obsolete MONDO:0015970)","secondary_identifiers":["Orphanet:183634"],"termid":"MONDO:0015970","xrefs":{"Monarch":{"xref_id":"0015970"}}}


id: GO:0047393
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycerol 1,2-cyclic phosphate + H2O = glycerol 1-phosphate + H+.","definition_xrefs":["EC:3.1.4.42","RHEA:16493"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoric diester hydrolase activity","termid":"GO:0008081"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016788"],"is_obsolete":false,"name":"glycerol-1,2-cyclic-phosphate 2-phosphodiesterase activity","secondary_identifiers":["MetaCyc:3.1.4.42-RXN","KEGG_REACTION:R02648"],"synonyms":[{"name":"rac-glycerol 1:2-cyclic phosphate 2-phosphodiesterase activity","type":"related"},{"name":"rac-glycerol-1,2-cyclic-phosphate 2-glycerophosphohydrolase activity","type":"related"}],"termid":"GO:0047393"}


id: GO:0140330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that reduces or removes the toxicity of a xenobiotic by exporting it outside the cell through the outer membrane.","definition_xrefs":["PMID:11948170"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xenobiotic transport","termid":"GO:0042908"},{"relation_name":"is_a","term_name":"export across cell outer membrane","termid":"GO:0140317"},{"relation_name":"part_of","term_name":"detoxification","termid":"GO:0098754"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0098754","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"xenobiotic detoxification by transmembrane export across the cell outer membrane","termid":"GO:0140330"}


id: MONDO:0033546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"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":"neurodegeneration, infantile-onset, biotin-responsive","secondary_identifiers":["MEDGEN:1771692","UMLS:C5436520","OMIM:618973"],"synonyms":[{"name":"NERIB","type":"exact"},{"name":"SMVT deficiency","type":"exact"},{"name":"sodium-dependent multivitamin transporter deficiency","type":"exact"}],"termid":"MONDO:0033546","xrefs":{"Monarch":{"xref_id":"0033546"}}}


id: PBO:0069237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 492, pseudogene","termid":"PBO:0069237"}


id: GO:1904024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glucose catabolic process to lactate via pyruvate.","definition_xrefs":["GOC:dph","PMID:20935145","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"negative regulation of fermentation","termid":"GO:1901003"},{"relation_name":"is_a","term_name":"regulation of glucose catabolic process to lactate via pyruvate","termid":"GO:1904023"},{"relation_name":"negatively_regulates","term_name":"glucose catabolic process to lactate via pyruvate","termid":"GO:0019661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"negatively_regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281","GO:0006091"],"is_obsolete":false,"name":"negative regulation of glucose catabolic process to lactate via pyruvate","synonyms":[{"name":"down regulation of glucose catabolic process to lactate via pyruvate","type":"exact"},{"name":"down regulation of glucose fermentation to lactate via pyruvate","type":"exact"},{"name":"down regulation of homofermentation","type":"exact"},{"name":"down regulation of homofermentative lactate fermentation","type":"exact"},{"name":"down regulation of homofermentative pathway","type":"exact"},{"name":"down regulation of homolactate fermentation","type":"exact"},{"name":"down regulation of homolactic fermentation","type":"exact"},{"name":"down-regulation of glucose catabolic process to lactate via pyruvate","type":"exact"},{"name":"down-regulation of glucose fermentation to lactate via pyruvate","type":"exact"},{"name":"down-regulation of homofermentation","type":"exact"},{"name":"down-regulation of homofermentative lactate fermentation","type":"exact"},{"name":"down-regulation of homofermentative pathway","type":"exact"},{"name":"down-regulation of homolactate fermentation","type":"exact"},{"name":"down-regulation of homolactic fermentation","type":"exact"},{"name":"downregulation of glucose catabolic process to lactate via pyruvate","type":"exact"},{"name":"downregulation of glucose fermentation to lactate via pyruvate","type":"exact"},{"name":"downregulation of homofermentation","type":"exact"},{"name":"downregulation of homofermentative lactate fermentation","type":"exact"},{"name":"downregulation of homofermentative pathway","type":"exact"},{"name":"downregulation of homolactate fermentation","type":"exact"},{"name":"downregulation of homolactic fermentation","type":"exact"},{"name":"inhibition of glucose catabolic process to lactate via pyruvate","type":"narrow"},{"name":"inhibition of glucose fermentation to lactate via pyruvate","type":"narrow"},{"name":"inhibition of homofermentation","type":"narrow"},{"name":"inhibition of homofermentative lactate fermentation","type":"narrow"},{"name":"inhibition of homofermentative pathway","type":"narrow"},{"name":"inhibition of homolactate fermentation","type":"narrow"},{"name":"inhibition of homolactic fermentation","type":"narrow"},{"name":"negative regulation of glucose fermentation to lactate via pyruvate","type":"exact"},{"name":"negative regulation of homofermentation","type":"exact"},{"name":"negative regulation of homofermentative lactate fermentation","type":"exact"},{"name":"negative regulation of homofermentative pathway","type":"exact"},{"name":"negative regulation of homolactate fermentation","type":"exact"},{"name":"negative regulation of homolactic fermentation","type":"exact"}],"termid":"GO:1904024"}


id: GO:0072342
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 anion stress, an increase or decrease in the concentration of negatively charged ions in the environment.","definition_xrefs":["GOC:cvs","PMID:19641131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to salt stress","termid":"GO:0009651"}],"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 anion stress","termid":"GO:0072342"}


id: PBO:0064604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POU class 3 homeobox 2","termid":"PBO:0064604"}


id: PBO:0112595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly protein, copper-binding, Cmc2","termid":"PBO:0112595"}


id: PBO:0046274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"essential meiotic structure-specific endonuclease 1","termid":"PBO:0046274"}


id: MONDO:0008232
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":"phagocytic cell dysfunction","termid":"MONDO:0024627"}],"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":"phagocytosis, plasma-related defect 1N","secondary_identifiers":["MESH:C566808","OMIM:171100","UMLS:C1868402","MEDGEN:356965"],"synonyms":[{"name":"phagocytosis, plasma-RELATED defect IN","type":"related"},{"name":"phagocytosis, plasma-related defect type 1N","type":"exact"}],"termid":"MONDO:0008232","xrefs":{"Monarch":{"xref_id":"0008232"}}}


id: PBO:0059266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L32","termid":"PBO:0059266"}


id: GO:0036417
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the stability of a tRNA molecule, making it more vulnerable to degradative processes.","definition_xrefs":["GOC:aa","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tRNA stability","termid":"GO:0036415"},{"relation_name":"is_a","term_name":"RNA destabilization","termid":"GO:0050779"},{"relation_name":"is_a","term_name":"positive regulation of tRNA catabolic process","termid":"GO:1902372"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006399"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006399"],"is_obsolete":false,"name":"tRNA destabilization","termid":"GO:0036417"}


id: GO:0006840
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of alpha-ketoglutarate and malate into, out of or within a mitochondrion.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial alpha-ketoglutarate/malate transport (obsolete GO:0006840)","synonyms":[{"name":"mitochondrial alpha-ketoglutarate/malate transport","type":"exact"},{"name":"mitochondrial oxoglutarate/malate transport","type":"exact"}],"termid":"GO:0006840"}


id: PBO:0086559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved among S. cerevisiae strains; YML122C is not an essential gene","termid":"PBO:0086559"}


id: GO:0102926
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + solanidine = H+ + gamma-chaconine + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete solanidine glucosyltransferase activity (obsolete GO:0102926)","termid":"GO:0102926"}


id: MONDO:0054837
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant non-syndromic intellectual disability","termid":"MONDO:0015802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual disability, autosomal dominant 57","secondary_identifiers":["UMLS:C4748003","OMIM:618050","MEDGEN:1648280"],"synonyms":[{"name":"MRD57","type":"related"},{"name":"TLK2-Related Neurodevelopmental Disorder","type":"exact"},{"name":"TLK2-related neurodevelopmental disorder","type":"exact"},{"name":"TLK2-related syndrome","type":"exact"},{"name":"intellectual developmental disorder, autosomal dominant 57","type":"exact"},{"name":"intellectual disability, autosomal dominant 57","type":"exact"},{"name":"mental retardation, autosomal dominant 57","type":"related"}],"termid":"MONDO:0054837","xrefs":{"Monarch":{"xref_id":"0054837"}}}


id: PBO:0083665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endoplasmic reticulum membrane protein; required for mannosylation of inositolphosphorylceramide and for growth at high calcium concentrations; protein abundance increases in response to DNA replication stress","termid":"PBO:0083665"}


id: PBO:0079634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2Q2 pseudogene 5, Y-linked","termid":"PBO:0079634"}


id: MONDO:0054846
data:
  {"annotated_genes":["SJAG_03042"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88137],"is_not":false,"summary":null,"term":"MONDO:0054846"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epilepsy, familial adult myoclonic","termid":"MONDO:0000160"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03042":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"epilepsy, familial adult myoclonic, 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618074","DOID:0111696","MEDGEN:1648448","UMLS:C4748079"],"synonyms":[{"name":"FAME6","type":"related"},{"name":"benign Adult Familial myoclonic epilepsy 6","type":"related"},{"name":"cortical myoclonic tremor with epilepsy, Familial, 6","type":"related"},{"name":"epilepsy, FAMILIAL ADULT myoclonic, 6","type":"related"}],"termid":"MONDO:0054846","terms_by_termid":{"MONDO:0054846":null},"xrefs":{"Monarch":{"xref_id":"0054846"}}}


id: PATO:0000244
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000244 ocular reflex (obsolete PATO:0000244)","termid":"PATO:0000244"}


id: PBO:0045100
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DMAC1 pseudogene 1","termid":"PBO:0045100"}


id: PBO:0091359
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dpb4-interacting, RRM and IDR-containing factor","termid":"PBO:0091359"}


id: GO:0000111
data:
  {"annotated_genes":["SJAG_01049","SJAG_01887"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73830,74339],"is_not":false,"summary":null,"term":"GO:0000111"}]},"cv_name":"cellular_component","definition":"One of several protein complexes involved in nucleotide-excision repair; possesses damaged DNA binding activity. In S. cerevisiae, it is composed of Rad4p and Rad23p.","definition_xrefs":["PMID:10915862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-excision repair complex","termid":"GO:0000109"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01049":null,"SJAG_01887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0032991"],"is_obsolete":false,"name":"nucleotide-excision repair factor 2 complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"NEF2 complex","type":"exact"}],"termid":"GO:0000111","terms_by_termid":{"GO:0000111":null}}


id: MONDO:0000352
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hereditary sensory neuropathy (obsolete MONDO:0000352)","termid":"MONDO:0000352","xrefs":{"Monarch":{"xref_id":"0000352"}}}


id: PR:O43058
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sep1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43058"],"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":"forkhead protein sep1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4C3.12","synonyms":[{"name":"Spom972h-sep1","type":"exact"}],"termid":"PR:O43058"}


id: PBO:0063912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha","termid":"PBO:0063912"}


id: MOD:01434
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to a 4-hydroxy-L-glutamic acid.","definition_xrefs":["ChEBI:141845","PubMed:893891","RESID:AA0487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monohydroxylated residue","termid":"MOD:00425"},{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-hydroxy-L-glutamic acid","synonyms":[{"name":"(2S,4Xi)-2-amino-4-hydroxypentanedioic acid","type":"exact"},{"name":"4-hydroxy-L-glutamic acid","type":"exact"},{"name":"MOD_RES 4-hydroxyglutamate","type":"exact"},{"name":"gamma-hydroxy glutaminic acid","type":"exact"},{"name":"threo-4-hydroxy-L-glutamic acid","type":"exact"}],"termid":"MOD:01434"}


id: MONDO:0001158
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by an enduring pattern of inflexibility, extreme orderliness, and perfectionism which interfere with efficiency and which may manifest in many different contexts, including work and leisure activities, financial matters, and issues of morality or ethics.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"personality disorder","termid":"MONDO:0002028"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"obsessive-compulsive personality disorder","secondary_identifiers":["ICD10CM:F60.5","ICD9:301.4","MESH:D003193","DOID:10932","UMLS:C0009595","SCTID:1376001","NCIT:C92638","MEDGEN:40432"],"synonyms":[{"name":"OCD","type":"exact"},{"name":"OCPD","type":"exact"},{"name":"anankastic personality disorder","type":"related"},{"name":"obsessional personality","type":"related"}],"termid":"MONDO:0001158","xrefs":{"Monarch":{"xref_id":"0001158"}}}


id: PATO:0000031
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000031 metabolite composition (obsolete PATO:0000031)","termid":"PATO:0000031"}


id: PBO:0029573
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_abnormal_morphology","termid":"PBO:0029573"}


id: PBO:0080451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-set and immunoglobulin domain containing 10 like 2","termid":"PBO:0080451"}


id: MONDO:0023664
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 54","secondary_identifiers":["DOID:0112335","MEDGEN:1782493","OMIM:619379","UMLS:C5543570"],"synonyms":[{"name":"SPGF54","type":"exact"}],"termid":"MONDO:0023664","xrefs":{"Monarch":{"xref_id":"0023664"}}}


id: PBO:0028249
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_actin_cytoskeleton","termid":"PBO:0028249"}


id: PBO:0043081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor nicotinic beta 1 subunit","termid":"PBO:0043081"}


id: PBO:0065708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudouridylate synthase 7 pseudogene 1","termid":"PBO:0065708"}


id: MONDO:0017533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"postaxial polydactyly type B","termid":"MONDO:0019674"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postaxial polydactyly type B, unilateral","secondary_identifiers":["icd11.foundation:154207037","Orphanet:295167"],"termid":"MONDO:0017533","xrefs":{"Monarch":{"xref_id":"0017533"}}}


id: GO:2001278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of L-leucine biosynthetic process.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"is_a","term_name":"positive regulation of amino acid biosynthetic process","termid":"GO:2000284"},{"relation_name":"is_a","term_name":"regulation of L-leucine biosynthetic process","termid":"GO:2001276"},{"relation_name":"positively_regulates","term_name":"L-leucine biosynthetic process","termid":"GO:0009098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"positive regulation of L-leucine biosynthetic process","synonyms":[{"name":"positive regulation of L-leucine anabolism","type":"exact"},{"name":"positive regulation of L-leucine biosynthesis","type":"exact"},{"name":"positive regulation of L-leucine formation","type":"exact"},{"name":"positive regulation of L-leucine synthesis","type":"exact"},{"name":"positive regulation of leucine biosynthetic process","type":"broad"}],"termid":"GO:2001278"}


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


id: PR:O74880
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An mRNA cap guanine-N7 methyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12189: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":"mRNA cap guanine-N7 methyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC330.10","secondary_identifiers":["UniProtKB:O74880"],"synonyms":[{"name":"SPCC330.10","type":"related"},{"name":"Spom972h-RNMT","type":"exact"},{"name":"mRNA (guanine-N(7)-)-methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"mRNA cap methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74880"}


id: MONDO:0011480
data:
  {"annotated_genes":["SJAG_03145"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87592],"is_not":false,"summary":null,"term":"MONDO:0011480"}]},"cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the ACTG1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03145":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 20","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0110550","OMIM:604717","GARD:18111","MEDGEN:346852","MESH:C565754","UMLS:C1858172"],"synonyms":[{"name":"ACTG1 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"DFNA20","type":"narrow"},{"name":"DFNA26","type":"narrow"},{"name":"autosomal dominant deafness 20","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 20","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in ACTG1","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 20","type":"narrow"},{"name":"deafness, autosomal dominant 20","type":"narrow"},{"name":"deafness, autosomal dominant 20/26","type":"narrow"},{"name":"deafness, autosomal dominant type 20","type":"narrow"}],"termid":"MONDO:0011480","terms_by_termid":{"MONDO:0011480":null},"xrefs":{"Monarch":{"xref_id":"0011480"}}}


id: PATO:0002021
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A convex 3-D shape quality inhering in a bearer by virtue of the bearer's resembling a cone (a 3-D shape with a round cross section that tapers).","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Cone_(geometry)"],"direct_ancestors":[{"relation_name":"is_a","term_name":"convex 3-D shape","termid":"PATO:0002007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conical","secondary_identifiers":["Image:http\\://upload.wikimedia.org/wikipedia/commons/d/d2/Cone_3d.png"],"synonyms":[{"name":"cone-shaped","type":"exact"}],"termid":"PATO:0002021"}


id: GO:1903488
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of lactation.","definition_xrefs":["GOC:TermGenie","GOC:mr","PMID:19563620","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of secretion","termid":"GO:0051048"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of lactation","termid":"GO:1903487"},{"relation_name":"negatively_regulates","term_name":"lactation","termid":"GO:0007595"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of lactation","synonyms":[{"name":"down regulation of lactation","type":"exact"},{"name":"down-regulation of lactation","type":"exact"},{"name":"downregulation of lactation","type":"exact"},{"name":"inhibition of lactation","type":"narrow"}],"termid":"GO:1903488"}


id: GO:0140789
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a phosphorylated histone + H2O = a protein + phosphate.","definition_xrefs":["PMID:19351884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoprotein phosphatase activity","termid":"GO:0004721"},{"relation_name":"is_a","term_name":"histone modifying activity","termid":"GO:0140993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0140096","GO:0016787","GO:0004721","GO:0016788","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"histone phosphatase activity","termid":"GO:0140789"}


id: PBO:0068605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 56, pseudogene","termid":"PBO:0068605"}


id: PBO:0053974
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 1285","termid":"PBO:0053974"}


id: PBO:0077430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 167A pseudogene 1","termid":"PBO:0077430"}


id: PBO:0046978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 86 member C1, pseudogene","termid":"PBO:0046978"}


id: GO:0032915
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of production of transforming growth factor-beta2.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transforming growth factor beta2 production","termid":"GO:0032909"},{"relation_name":"is_a","term_name":"positive regulation of transforming growth factor beta production","termid":"GO:0071636"},{"relation_name":"positively_regulates","term_name":"transforming growth factor beta2 production","termid":"GO:0032906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of transforming growth factor beta2 production","synonyms":[{"name":"activation of transforming growth factor-beta2 production","type":"narrow"},{"name":"positive regulation of TGF-B2 production","type":"exact"},{"name":"positive regulation of TGFB2 production","type":"exact"},{"name":"positive regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"stimulation of transforming growth factor-beta2 production","type":"narrow"},{"name":"up regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"up-regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"upregulation of transforming growth factor-beta2 production","type":"exact"}],"termid":"GO:0032915"}


id: PBO:0065063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"perforin 1","termid":"PBO:0065063"}


id: GO:0001770
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed orientation of natural killer cell signaling molecules and associated membrane rafts towards a chemokine gradient or a contact point with a cell displaying natural killer cell activating ligands.","definition_xrefs":["PMID:12615886","GOC:mgi_curators","PMID:9759849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of lymphocyte polarity","termid":"GO:0001767"},{"relation_name":"part_of","term_name":"natural killer cell activation","termid":"GO:0030101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"establishment of natural killer cell polarity","synonyms":[{"name":"NK cell polarization","type":"exact"},{"name":"establishment of NK cell polarity","type":"exact"},{"name":"natural killer cell polarization","type":"exact"}],"termid":"GO:0001770"}


id: PBO:0064714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 50","termid":"PBO:0064714"}


id: PBO:0031910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridylate kinase Ura6 (predicted)","termid":"PBO:0031910"}


id: PBO:0092024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Glutamine (uug), mitochondrial","termid":"PBO:0092024"}


id: PBO:0043656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COPI coat complex subunit zeta 2","termid":"PBO:0043656"}


id: PBO:0049221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor kinase 4","termid":"PBO:0049221"}


id: MONDO:0024471
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-inflammatory vasculopathy (obsolete MONDO:0024471)","secondary_identifiers":["Orphanet:496924"],"termid":"MONDO:0024471","xrefs":{"Monarch":{"xref_id":"0024471"}}}


id: PR:Q9UUJ9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A propionyl-CoA:succinate CoA transferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02074"],"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":"acetyl-CoA hydrolase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1952.09c","secondary_identifiers":["UniProtKB:Q9UUJ9"],"synonyms":[{"name":"Spom972h-scpC","type":"exact"},{"name":"acetyl-CoA acylase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"acetyl-CoA deacylase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UUJ9"}


id: MONDO:0003946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenoma that arises from the vagina and is characterized by a villous architectural pattern.","definition_xrefs":["NCIT:C40259"],"direct_ancestors":[{"relation_name":"is_a","term_name":"villous adenoma","termid":"MONDO:0000502"},{"relation_name":"is_a","term_name":"vaginal adenoma","termid":"MONDO:0003434"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vaginal villous adenoma","secondary_identifiers":["MEDGEN:275577","UMLS:C1519936","DOID:6613"],"synonyms":[{"name":"vagina villous adenoma","type":"exact"},{"name":"vaginal villous adenoma","type":"exact"}],"termid":"MONDO:0003946","xrefs":{"Monarch":{"xref_id":"0003946"}}}


id: PBO:0017503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-glutamate O-methyltransferase (predicted)","termid":"PBO:0017503"}


id: PBO:0048803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit alpha transducin 3","termid":"PBO:0048803"}


id: PBO:0086128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for high temperature survival during stationary phase; not required for growth on nonfermentable carbon sources; SWAT-GFP and mCherry fusion proteins localize to the endoplasmic reticulum","termid":"PBO:0086128"}


id: GO:1903968
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 micafungin stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:16928959"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to micafungin","termid":"GO:1903967"}],"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 micafungin","termid":"GO:1903968"}


id: PBO:0050348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 51","termid":"PBO:0050348"}


id: MONDO:0017508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital absence/hypoplasia of fingers excluding thumb, bilateral (obsolete MONDO:0017508)","secondary_identifiers":["Orphanet:295114"],"synonyms":[{"name":"Adactyly of hand, bilateral","type":"exact"},{"name":"digits 2-5 hypodactyly, bilateral","type":"exact"},{"name":"digits 2-5 oligodactyly, bilateral","type":"exact"}],"termid":"MONDO:0017508","xrefs":{"Monarch":{"xref_id":"0017508"}}}


id: MONDO:0100020
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A childhood-onset epilepsy that is characterized by frequent seizures of multiple types, including nocturnal focal motor and fronto-parietal opercular seizures, and daytime focal motor seizures with negative myoclonus and atypical absence seizures. Centrotemporal sharp waves are seen on EEG. During the phase of the epilepsy when seizures are frequent, neuropsychological deficits and motor impairment may be present. These deficits improve when seizures remit.","direct_ancestors":[{"relation_name":"is_a","term_name":"childhood-onset epilepsy syndrome","termid":"MONDO:0020072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"atypical childhood epilepsy with centrotemporal spikes","synonyms":[{"name":"atonic-benign childhood epilepsy with centrotemporal spikes","type":"exact"},{"name":"atypical benign partial epilepsy of childhood","type":"exact"},{"name":"pseudo-Lennox syndrome","type":"exact"}],"termid":"MONDO:0100020","xrefs":{"Monarch":{"xref_id":"0100020"}}}


id: _global:regulates_o_has_agent
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"A relationship between the regulation of a process and the agent that executes that process.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulates_o_has_agent","secondary_identifiers":["GOREL:0001011"],"synonyms":[{"name":"regulates_o_has_agent","type":"exact"}],"termid":"_global:regulates_o_has_agent"}


id: SO:0001373
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"1_methyl_3_3_amino_3_carboxypropyl_pseudouridine 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":"one_methyl_three_three_amino_three_carboxypropyl_pseudouridine","secondary_identifiers":["RNAMOD:086"],"synonyms":[{"name":"1-methyl-3-(3-amino-3-carboxypropyl) pseudouridine","type":"exact"},{"name":"m1acp3Y","type":"exact"}],"termid":"SO:0001373"}


id: PBO:0070775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 5","termid":"PBO:0070775"}


id: PBO:0045604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 15 (pseudogene)","termid":"PBO:0045604"}


id: GO:0140162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism initiates, promotes, or enhances vasodilation via the action of a venom that activates bradykinin-dependent signaling, concomittantly reducing blood pressure in the bitten/stung organism. This can take place via several mechanisms that affect endogenous bradykinin: either increasing its release by kallikrein-like proteases, increasing bradykinin action by potentiation, or inhibiting bradykinin degradation.","definition_xrefs":["PMID:31370142"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of G protein-coupled receptor signaling pathway","termid":"GO:0044513"},{"relation_name":"is_a","term_name":"venom-mediated vasodilation","termid":"GO:0044551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"venom-mediated vasodilation by activation of bradykinin-dependent signaling","synonyms":[{"name":"venom-mediated vasodilation through activity of bradykinin","type":"exact"}],"termid":"GO:0140162"}


id: MOD:00416
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A change resulting in an alteration of the measured molecular mass of a peptide or protein hydroxyl amino acid phosphorylated promptly followed by secondary loss of a neutral trihydrogen phosphate molecular fragment.","definition_xrefs":["Unimod:23"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified residue with neutral loss of phosphate","termid":"MOD:00432"},{"relation_name":"is_a","term_name":"dehydrated residue","termid":"MOD:00704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphorylation of an hydroxyl amino acid with prompt loss of phosphate","synonyms":[{"name":"Dehydrated","type":"related"},{"name":"Dehydration","type":"related"}],"termid":"MOD:00416"}


id: PBO:0055996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long stress-induced non-coding transcript 5","termid":"PBO:0055996"}


id: PBO:0083650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endochitinase; required for cell separation after mitosis; transcriptional activation during the G1 phase of the cell cycle is mediated by transcription factor Ace2p","termid":"PBO:0083650"}


id: MONDO:0014726
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the SPG11 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease axonal type 2X","secondary_identifiers":["UMLS:C5569024","EFO:1001983","DOID:0110176","Orphanet:466775","GARD:17830","MEDGEN:1800447","OMIM:616668"],"synonyms":[{"name":"ARCMT2X","type":"exact"},{"name":"CMT2X","type":"exact"},{"name":"Charcot-Marie-Tooth disease caused by mutation in SPG11","type":"exact"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2X","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2X","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2x","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy type 2X","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 2X","type":"related"},{"name":"SPG11 Charcot-Marie-Tooth disease","type":"exact"},{"name":"autosomal recessive Charcot Marie Tooth disease type 2X","type":"related"},{"name":"autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation","type":"exact"},{"name":"autosomal recessive Charcot-Marie-Tooth disease type 2X","type":"related"},{"name":"autosomal recessive axonal Charcot-Marie-Tooth disease type 2X","type":"exact"}],"termid":"MONDO:0014726","xrefs":{"Monarch":{"xref_id":"0014726"}}}


id: FYPO:0007679
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which replication fork arrest at the RTS1 barrier (normally located in the mating-type region) occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah","PMID:33568651"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal replication fork arrest","termid":"FYPO:0003088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased replication fork arrest at RTS1 barrier","termid":"FYPO:0007679"}


id: MONDO:0006119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extranodal marginal zone B-cell lymphoma of mucosa associated lymphoid tissue that arises from the breast as a primary tumor.","definition_xrefs":["NCIT:C35688"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"MALT lymphoma","termid":"MONDO:0007650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"breast mucosa-associated lymphoid tissue lymphoma","secondary_identifiers":["UMLS:C1332633","MEDGEN:234051"],"synonyms":[{"name":"breast MALT lymphoma","type":"exact"},{"name":"breast mucosa-associated lymphoid tissue lymphoma","type":"exact"}],"termid":"MONDO:0006119","xrefs":{"Monarch":{"xref_id":"0006119"}}}


id: PBO:0083379
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 ALT2/YDR111C; null mutant displays increased levels of spontaneous Rad52p foci","termid":"PBO:0083379"}


id: PBO:0120053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial RNA degradosome protein Pet127","termid":"PBO:0120053"}


id: PBO:0084850
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; involved together with Mrpl35p in assembly of cytochrome c oxidase","termid":"PBO:0084850"}


id: PBO:0060370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myotilin","termid":"PBO:0060370"}


id: MONDO:0013975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any pure hair and nail ectodermal dysplasia in which the cause of the disease is a mutation in the KRT74 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pure hair and nail ectodermal dysplasia","termid":"MONDO:0019071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"ectodermal dysplasia 7, hair/nail type","secondary_identifiers":["OMIM:614929","DOID:0111660","UMLS:C3554117","GARD:18065","MEDGEN:767031"],"synonyms":[{"name":"ECTD7","type":"related"},{"name":"KRT74 pure hair and nail ectodermal dysplasia","type":"exact"},{"name":"ectodermal dysplasia 7, hair/nail type","type":"exact"},{"name":"pure hair and nail ectodermal dysplasia caused by mutation in KRT74","type":"exact"}],"termid":"MONDO:0013975","xrefs":{"Monarch":{"xref_id":"0013975"}}}


id: PBO:0069285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 541, pseudogene","termid":"PBO:0069285"}


id: PBO:0076136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUCLA2 pseudogene 1","termid":"PBO:0076136"}


id: SO:0000680
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A start codon that is not the usual AUG sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"start_codon","termid":"SO:0000318"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non_canonical_start_codon","synonyms":[{"name":"non ATG start codon","type":"exact"},{"name":"non canonical start codon","type":"exact"},{"name":"non-canonical start codon","type":"exact"}],"termid":"SO:0000680"}


id: FYPO:0008406
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 endoplasmic reticulum is abnorma and some of the protein is present in the cytoplasmic aggregates instead.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0003777"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal protein localization to endoplasmic reticulum with cytoplasmic aggregation","termid":"FYPO:0008406"}


id: MONDO:0958352
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare open neural tube defect characterized by no other malformation than myeloschisis (spina bifida with a neural placode exposed at or below the skin plane and Chiari II malformation).","definition_xrefs":["Orphanet:645401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloschisis","termid":"MONDO:0958076"}],"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":"true myeloschisis","secondary_identifiers":["MEDGEN:1853154","UMLS:C5816711"],"termid":"MONDO:0958352","xrefs":{"Monarch":{"xref_id":"0958352"}}}


id: MOD:00129
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-retinylidene-L-lysine, the adduct of retinal.","definition_xrefs":["PubMed:6794028","PubMed:6870827","Unimod:380#K","RESID:AA0120"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N6-retinylidene-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-[(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)-2,4,6,8-nonatetraenylidene]aminohexanoic acid","type":"exact"},{"name":"MOD_RES N6-(retinylidene)lysine","type":"exact"},{"name":"N6-retinal-L-lysine","type":"exact"},{"name":"N6-retinyl-lysine","type":"exact"},{"name":"N6-retinylidene-L-lysine","type":"exact"},{"name":"N6RetalLys","type":"exact"},{"name":"Retinylidene","type":"related"},{"name":"retinal","type":"related"}],"termid":"MOD:00129"}


id: GO:0044201
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The inner, i.e. lumen-facing, lipid bilayer of the host nuclear envelope.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell nuclear membrane","termid":"GO:0044200"}],"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 nuclear inner membrane","termid":"GO:0044201"}


id: PBO:0058737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6862-1","termid":"PBO:0058737"}


id: PBO:0090186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein Crt10, involved in ribosomal RNA decay","termid":"PBO:0090186"}


id: MONDO:0004601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ulcer of lower limbs is a chronic ulcer of skin where the ulcer is not a decubitus ulcer.","definition_xrefs":["DOID:8529"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic ulcer of skin","termid":"MONDO:0004605"}],"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":"ulcer of lower limbs","secondary_identifiers":["ICD9:707.13","MEDGEN:9701","SCTID:419193008","UMLS:C0023223"],"synonyms":[{"name":"Ulcer of ankle","type":"narrow"},{"name":"Ulcer of calf","type":"narrow"},{"name":"Ulcer of heel and midfoot","type":"narrow"},{"name":"Ulcer of thigh","type":"narrow"}],"termid":"MONDO:0004601","xrefs":{"Monarch":{"xref_id":"0004601"}}}


id: PBO:0053677
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 862","termid":"PBO:0053677"}


id: MOD:02027
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks the N6-amino of a peptidyl lysine with the carboxyl-terminal glycine of a URM1 protein.","definition_xrefs":["PubMed:10713047","PubMed:21209336"],"direct_ancestors":[{"relation_name":"contains","term_name":"N6-glycyl-L-lysine","termid":"MOD:00134"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"},{"relation_name":"is_a","term_name":"crosslinked L-lysine residue","termid":"MOD:02051"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"urmylated lysine","termid":"MOD:02027"}


id: GO:0060357
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, frequency or extent of leucine import. Leucine import is the directed movement of leucine into a cell or organelle.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of L-leucine import (obsolete GO:0060357)","synonyms":[{"name":"regulation of L-leucine import","type":"narrow"},{"name":"regulation of L-leucine uptake","type":"narrow"},{"name":"regulation of leucine import","type":"broad"},{"name":"regulation of leucine uptake","type":"exact"}],"termid":"GO:0060357"}


id: PR:O94523
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1281.06c gene.","definition_xrefs":["UniProtKB:O94523","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":"acyl-CoA desaturase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1281.06c","synonyms":[{"name":"Spom972h-SPCC1281.06c","type":"exact"},{"name":"delta(9)-desaturase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"delta-9 desaturase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"fatty acid desaturase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"stearoyl-CoA desaturase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94523"}


id: PBO:0087629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the Dcp1p-Dcp2p decapping enzyme complex; decapping complex removes the 5' cap structure from mRNAs prior to their degradation; enhances the activity of catalytic subunit Dcp2p; regulated by DEAD box protein Dhh1p; forms cytoplasmic foci upon DNA replication stress","termid":"PBO:0087629"}


id: MONDO:0958104
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Alport syndrome","termid":"MONDO:0018965"}],"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":"digenic Alport syndrome","secondary_identifiers":["Orphanet:653722","MEDGEN:1863937","UMLS:C5925113"],"termid":"MONDO:0958104","xrefs":{"Monarch":{"xref_id":"0958104"}}}


id: PBO:0059747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 21","termid":"PBO:0059747"}


id: PBO:0067669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 849, pseudogene","termid":"PBO:0067669"}


id: PBO:0041631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CACNA1C antisense RNA 1","termid":"PBO:0041631"}


id: MONDO:0014522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066","MONDO:0005328"],"is_obsolete":false,"name":"retinal dystrophy and obesity","secondary_identifiers":["OMIM:616188","UMLS:C4015424","MEDGEN:863861"],"synonyms":[{"name":"RDOB","type":"related"},{"name":"retinal dystrophy and obesity","type":"exact"}],"termid":"MONDO:0014522","xrefs":{"Monarch":{"xref_id":"0014522"}}}


id: PBO:0080745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X antigen family member 1A","termid":"PBO:0080745"}


id: MONDO:0004932
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute lymphoblastic leukemia","termid":"MONDO:0004967"}],"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":"null-cell leukemia","secondary_identifiers":["DOID:9954","MEDGEN:507917","SCTID:277574007","UMLS:C0023483"],"synonyms":[{"name":"null cell acute lymphoblastic leukaemia","type":"exact"},{"name":"null cell acute lymphoblastic leukemia","type":"exact"}],"termid":"MONDO:0004932","xrefs":{"Monarch":{"xref_id":"0004932"}}}


id: GO:0035173
data:
  {"annotated_genes":["SJAG_00678","SJAG_01837","SJAG_00364","SJAG_01082","SJAG_03720"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[118077,108435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140995"},{"annotations":[116342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072371"},{"annotations":[118528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035175"},{"annotations":[79933],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072354"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a phosphate group to a histone.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase activity","termid":"GO:0004672"},{"relation_name":"is_a","term_name":"histone modifying activity","termid":"GO:0140993"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_00678":null,"SJAG_01082":null,"SJAG_01837":null,"SJAG_03720":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0004672","GO:0016740","GO:0003674","GO:0003824","GO:0016301","GO:0140096"],"is_obsolete":false,"name":"histone kinase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0035173","terms_by_termid":{"GO:0035175":null,"GO:0072354":null,"GO:0072371":null,"GO:0140995":null}}


id: MONDO:0800066
data:
  {"annotated_genes":["SJAG_01213"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010408"}]},"cv_name":"mondo","definition":"Any skeletal dysplasia that is characterizedby polydactyly, syndactyly and triphalangism, where a digit has three phalanges instead of two.","definition_xrefs":["PMID:19125433","PMID:31633310"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"},{"relation_name":"is_a","term_name":"syndactyly","termid":"MONDO:0021002"},{"relation_name":"is_a","term_name":"polydactyly","termid":"MONDO:0021003"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01213":null},"genotype_count":0,"is_obsolete":false,"name":"polydactyly-syndactyly-triphalangism","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0800066","terms_by_termid":{"MONDO:0010408":null},"xrefs":{"Monarch":{"xref_id":"0800066"}}}


id: MONDO:0034143
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"osteopetrosis","termid":"MONDO:0017198"},{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"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":"early-onset calcifying leukoencephalopathy-skeletal dysplasia","secondary_identifiers":["UMLS:C5681333","GARD:22246","MEDGEN:1805057","Orphanet:556985"],"termid":"MONDO:0034143","xrefs":{"Monarch":{"xref_id":"0034143"}}}


id: GO:1903218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of malate dehydrogenase (decarboxylating) (NADP+) activity.","definition_xrefs":["GO_REF:0000059","GOC:sart","GOC:TermGenie","PMID:12398416"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of malate dehydrogenase (decarboxylating) (NADP+) activity (obsolete GO:1903218)","synonyms":[{"name":"regulation of 'malic' enzyme","type":"related"},{"name":"regulation of (S)-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating)","type":"exact"},{"name":"regulation of L-malate:NADP oxidoreductase activity","type":"exact"},{"name":"regulation of NADP-linked decarboxylating malic enzyme","type":"related"},{"name":"regulation of NADP-malic enzyme activity","type":"exact"},{"name":"regulation of NADP-specific malate dehydrogenase activity","type":"exact"},{"name":"regulation of NADP-specific malic enzyme","type":"related"},{"name":"regulation of malate dehydrogenase (NADP, decarboxylating)","type":"exact"},{"name":"regulation of malate dehydrogenase (decarboxylating, NADP)","type":"exact"}],"termid":"GO:1903218"}


id: PR:P05933
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A calmodulin that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00584","PANTHER:PTHR23050:SF20","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":"calmodulin (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A12.14","secondary_identifiers":["UniProtKB:P05933"],"synonyms":[{"name":"CaM (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CALM","type":"exact"}],"termid":"PR:P05933"}


id: PBO:0039391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"archaelysin family metallopeptidase 2","termid":"PBO:0039391"}


id: GO:0035970
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of phosphoric residues from peptidyl-O-phospho-L-threonine to form peptidyl-threonine.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein dephosphorylation","termid":"GO:0006470"}],"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":"peptidyl-threonine dephosphorylation","termid":"GO:0035970"}


id: PBO:0040286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase Na+/K+ transporting subunit beta 1 pseudogene 1","termid":"PBO:0040286"}


id: MOD:00937
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Post-translational","definition_xrefs":["Unimod:505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"levuglandinyl (prostaglandin H2) adduct","termid":"MOD:00846"},{"relation_name":"is_a","term_name":"modified L-arginine residue","termid":"MOD:00902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Levuglandinyl - arginine lactam adduct","synonyms":[{"name":"LG-lactam-R","type":"related"},{"name":"Levuglandinyl - arginine lactam adduct","type":"related"}],"termid":"MOD:00937"}


id: MONDO:0006003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the body of uterus.","direct_ancestors":[{"relation_name":"is_a","term_name":"uterine cancer","termid":"MONDO:0002715"},{"relation_name":"is_a","term_name":"corpus uteri neoplasm","termid":"MONDO:0021254"}],"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":"uterine corpus cancer","secondary_identifiers":["SCTID:371972005","ICD9:182","MEDGEN:364875","NCIT:C61574","UMLS:C1883486","DOID:9460","EFO:0007532"],"synonyms":[{"name":"body of uterus cancer","type":"exact"},{"name":"cancer of body of uterus","type":"exact"},{"name":"cancer of the corpus uteri","type":"exact"},{"name":"corpus uteri cancer","type":"exact"},{"name":"endometrial cancer","type":"related"},{"name":"malignant body of uterus neoplasm","type":"exact"},{"name":"malignant neoplasm of body of uterus","type":"exact"},{"name":"uterine (including endometrial) cancer","type":"exact"},{"name":"uterine corpus cancer","type":"exact"}],"termid":"MONDO:0006003","xrefs":{"Monarch":{"xref_id":"0006003"}}}


id: MONDO:0008920
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":"carnitine deficiency, myopathic","secondary_identifiers":["UMLS:C1859318","MESH:C536100","OMIM:212160","MEDGEN:347852"],"synonyms":[{"name":"carnitine deficiency, myopathic","type":"exact"},{"name":"myopathic carnitine deficiency","type":"related"}],"termid":"MONDO:0008920","xrefs":{"Monarch":{"xref_id":"0008920"}}}


id: MONDO:0006598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dermatitis caused or precipitated by exposure to ultraviolet sunlight, or by mediating phototoxic or photoallergic material in response to ultraviolet sunlight.","definition_xrefs":["NCIT:C4816"],"direct_ancestors":[{"relation_name":"is_a","term_name":"irritant dermatitis","termid":"MONDO:0006564"},{"relation_name":"is_a","term_name":"photosensitivity disease","termid":"MONDO:0006597"}],"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":"phototoxic dermatitis","secondary_identifiers":["Wikipedia:Photodermatitis","DOID:4407","EFO:1000753","MEDGEN:58188","MESH:D017484","SCTID:53597009","UMLS:C0162830"],"synonyms":[{"name":"Photodermatitis","type":"exact"},{"name":"Photosensitisation reaction","type":"exact"},{"name":"photosensitive dermatitis","type":"exact"},{"name":"photosensitiveness","type":"exact"},{"name":"photosensitivity reaction","type":"exact"}],"termid":"MONDO:0006598","xrefs":{"Monarch":{"xref_id":"0006598"}}}


id: PBO:0038594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA dehydrogenase long chain","termid":"PBO:0038594"}


id: PBO:0050945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon alpha 17","termid":"PBO:0050945"}


id: GO:0050010
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: isovitexin + UDP-D-glucose = H+ + isovitexin 2''-O-beta-D-glucoside + UDP.","definition_xrefs":["RHEA:19529","EC:2.4.1.106"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"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:0016757","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"isovitexin beta-glucosyltransferase activity","secondary_identifiers":["KEGG_REACTION:R03686","MetaCyc:ISOVITEXIN-BETA-GLUCOSYLTRANSFERASE-RXN"],"synonyms":[{"name":"UDP-glucose:isovitexin 2''-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:isovitexin 2''-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"isovitexin b-glucosyltransferase activity","type":"exact"},{"name":"uridine diphosphoglucose-isovitexin 2''-glucosyltransferase activity","type":"related"}],"termid":"GO:0050010"}


id: PBO:0059781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 7","termid":"PBO:0059781"}


id: PBO:0038824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 30","termid":"PBO:0038824"}


id: PBO:0088277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"delta-1-pyrroline-5-carboxylate reductase Pro3","termid":"PBO:0088277"}


id: PBO:0077339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 78","termid":"PBO:0077339"}


id: MONDO:0025425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A contagious disease caused by canine adenovirus (adenoviruses, canine) infecting the liver, the eye, the kidney, and other organs in dogs, other canids, and bears. Symptoms include fever; edema; vomiting; and diarrhea.","definition_xrefs":["MESH:D006522"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dog disease","termid":"MONDO:0024919"},{"relation_name":"is_a","term_name":"hepatitis, viral, animal","termid":"MONDO:0025085"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hepatitis, infectious canine","synonyms":[{"name":"Hepatitides, canine infectious","type":"related"},{"name":"Hepatitides, infectious canine","type":"related"},{"name":"Hepatitis, canine infectious","type":"related"},{"name":"canine Hepatitides, infectious","type":"related"},{"name":"canine Hepatitis, infectious","type":"related"},{"name":"canine infectious Hepatitides","type":"related"},{"name":"canine infectious Hepatitis","type":"related"},{"name":"infectious Hepatitides, canine","type":"related"},{"name":"infectious Hepatitis, canine","type":"related"},{"name":"infectious canine Hepatitides","type":"related"},{"name":"infectious canine Hepatitis","type":"related"}],"termid":"MONDO:0025425","xrefs":{"Monarch":{"xref_id":"0025425"}}}


id: FYPO:0002658
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of trehalose 6-phosphate measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular trehalose 6-phosphate level","synonyms":[{"name":"increased cellular trehalose 6-phosphate level during mitotic cell cycle","type":"related"},{"name":"increased cellular trehalose 6-phosphate level during vegetative growth","type":"exact"},{"name":"increased cellular trehalose-6P level","type":"exact"},{"name":"increased trehalose 6-phosphate accumulation","type":"related"}],"termid":"FYPO:0002658"}


id: MONDO:0005609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A common dermal and neurologic disorder caused by reactivation of the varicella-zoster virus that has remained dormant within dorsal root ganglia, often for decades, after the patient's initial exposure to the virus in the form of varicella (chickenpox). It is characterized by severe neuralgic pain along the distribution of the affected nerve and crops of clustered vesicles over the area.","definition_xrefs":["NCIT:C71079"],"direct_ancestors":[{"relation_name":"is_a","term_name":"varicella zoster infection","termid":"MONDO:0005608"},{"relation_name":"is_a","term_name":"vesiculobullous skin disease","termid":"MONDO:0006617"},{"relation_name":"is_a","term_name":"post-viral disorder","termid":"MONDO:0021674"},{"relation_name":"is_a","term_name":"skin disorder caused by infection","termid":"MONDO:0024294"},{"relation_name":"is_a","term_name":"disease arising from reactivation of latent virus","termid":"MONDO:0100330"}],"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":"herpes zoster","secondary_identifiers":["ICD10CM:B02","SCTID:4740000","DOID:8536","ICD9:053","MEDGEN:42437","EFO:0006510","MESH:D006562","UMLS:C0019360"],"synonyms":[{"name":"Zoster","type":"exact"},{"name":"herpes Zoster","type":"exact"},{"name":"herpes zona","type":"exact"},{"name":"postherpetic neuralgia","type":"related"},{"name":"shingles","type":"exact"}],"termid":"MONDO:0005609","xrefs":{"Monarch":{"xref_id":"0005609"}}}


id: PBO:0044118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTAGE family member 3, pseudogene","termid":"PBO:0044118"}


id: PR:O94493
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC417.12 gene.","definition_xrefs":["UniProtKB:O94493","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized esterase/lipase C417.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC417.12","synonyms":[{"name":"Spom972h-SPCC417.12","type":"exact"}],"termid":"PR:O94493"}


id: PBO:0069628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 905, pseudogene","termid":"PBO:0069628"}


id: MONDO:0021530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the subglottis.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"subglottis neoplasm","termid":"MONDO:0000933"},{"relation_name":"is_a","term_name":"benign laryngeal neoplasm","termid":"MONDO:0002354"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of subglottis","secondary_identifiers":["UMLS:C0345749","NCIT:C4427","SCTID:92412003","MEDGEN:83388"],"synonyms":[{"name":"benign neoplasm of the subglottis","type":"exact"},{"name":"benign subglottic neoplasm","type":"exact"},{"name":"benign subglottic tumor","type":"exact"},{"name":"benign subglottic tumour","type":"exact"},{"name":"benign subglottis neoplasm","type":"exact"},{"name":"benign subglottis tumor","type":"exact"},{"name":"benign subglottis tumour","type":"exact"},{"name":"benign tumor of subglottis","type":"exact"},{"name":"benign tumor of the subglottis","type":"exact"},{"name":"benign tumour of subglottis","type":"exact"},{"name":"benign tumour of the subglottis","type":"exact"},{"name":"subglottis benign neoplasm","type":"exact"}],"termid":"MONDO:0021530","xrefs":{"Monarch":{"xref_id":"0021530"}}}


id: GO:0007348
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cell cycle process that modulates the rate or extent of the progression through the syncytial blastoderm mitotic cell cycle.","definition_xrefs":["GOC:tb","GOC:dph","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle, embryonic","termid":"GO:0009794"},{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"regulates","term_name":"syncytial blastoderm mitotic cell cycle","termid":"GO:0035186"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of syncytial blastoderm mitotic cell cycle","synonyms":[{"name":"modulation of syncytial blastoderm cell cycle progression","type":"exact"},{"name":"regulation of progression through syncytial blastoderm mitotic cell cycle","type":"exact"},{"name":"regulation of syncytial blastoderm cell cycle","type":"exact"},{"name":"regulation of syncytial blastoderm cell cycle progression","type":"exact"},{"name":"syncytial blastoderm cell cycle modulation","type":"exact"},{"name":"syncytial blastoderm cell cycle regulation","type":"exact"},{"name":"syncytial blastoderm cell cycle regulator","type":"related"}],"termid":"GO:0007348"}


id: PBO:0049081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 137","termid":"PBO:0049081"}


id: GO:0030297
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases the activity of a transmembrane receptor protein tyrosine kinase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein tyrosine kinase activator activity","termid":"GO:0030296"},{"relation_name":"is_a","term_name":"signaling receptor activator activity","termid":"GO:0030546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140677","GO:0030234","GO:0003674","GO:0098772"],"is_obsolete":false,"name":"transmembrane receptor protein tyrosine kinase activator activity","termid":"GO:0030297"}


id: PBO:0055729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM domain only 3","termid":"PBO:0055729"}


id: PBO:0064690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 26","termid":"PBO:0064690"}


id: PBO:0091162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ReqQ-type subtelomeric helicase fragment","termid":"PBO:0091162"}


id: SO:0002111
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A processed_transcript supported by EST and/or mRNA evidence that aligns unambiguously to a pseudogene locus (i.e. alignment to the pseudogene locus clearly better than alignment to parent locus).","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"processed_transcript","termid":"SO:0001503"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudogene_processed_transcript","synonyms":[{"name":"pseudogene processed transcript","type":"exact"}],"termid":"SO:0002111"}


id: MONDO:0009581
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome is characterized by moderate intellectual deficit, craniofacial dysmorphism (including broad nose with coloboma of the alea nasi, deep-set eyes, prognathism), hypergonadotropic hypogonadism, eunuchoid habitus, type 1 diabetes mellitus, and epilepsy. It has been described in four patients (three brothers and their sister). This syndrome is probably transmitted as an autosomal recessive trait.","definition_xrefs":["Orphanet:3044"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome","secondary_identifiers":["OMIM:249599","GARD:9811","MEDGEN:343317","UMLS:C1855303","MESH:C537447","SCTID:722454003"],"synonyms":[{"name":"Belgian type intellectual disability syndrome","type":"related"},{"name":"Belgian type mental retardation syndrome","type":"related"},{"name":"intellectual disability syndrome, Belgian type","type":"related"},{"name":"mental retardation syndrome, Belgian type","type":"related"}],"termid":"MONDO:0009581","xrefs":{"Monarch":{"xref_id":"0009581"}}}


id: GO:0071619
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of introducing a phosphate group onto a serine residue at position 2 within the heptapeptide repeat (YSPTSPS) of the C-terminal domain of RNA polymerase II. Typically, phosphorylation of serine 2 (Ser2) occurs subsequent to phosphorylation of serine 5 and is thus seen in the middle and 3' ends of genes. In vivo, Ser2 phosphorylation is primarily performed by CTDK-I in S. cerevisiae or CDK9 in metazoans.","definition_xrefs":["GOC:krc","PMID:17079683"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphorylation of RNA polymerase II C-terminal domain serine 2 residues (obsolete GO:0071619)","termid":"GO:0071619"}


id: PBO:0056763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase like 15 pseudogene 2","termid":"PBO:0056763"}


id: PBO:0026752
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_phosphorylation_during_cellular_response_to_arginine","termid":"PBO:0026752"}


id: MONDO:1012075
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple exostoses, non-human animal","termid":"MONDO:1011944"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple exostoses, pig","secondary_identifiers":["OMIA:000354-9823"],"termid":"MONDO:1012075","xrefs":{"Monarch":{"xref_id":"1012075"}}}


id: PBO:0035998
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K9_methylation_at_silent_mating-type_cassette_during_vegetative_growth","termid":"PBO:0035998"}


id: GO:0120201
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Stack of disc membranes located inside a cone photoreceptor outer segment, and containing densely packed molecules of opsin photoreceptor proteins that traverse the lipid bilayer. Cone disc membranes arise as evaginations of the ciliary membrane during the development of the cone outer segment and remain contiguous with the ciliary membrane.","definition_xrefs":["GOC:krc","PMID:19501669","PMID:6771304","GOC:pde","PMID:26574505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary membrane","termid":"GO:0060170"},{"relation_name":"is_a","term_name":"photoreceptor disc membrane","termid":"GO:0097381"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"cone photoreceptor disc membrane","termid":"GO:0120201"}


id: GO:0097180
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex that contains a serine protease inhibitor and a protease; formation of the complex inhibits serine protease activity.","definition_xrefs":["PMID:6323392","GOC:ans"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protease inhibitor complex","termid":"GO:0097179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"serine protease inhibitor complex","synonyms":[{"name":"serine-type endopeptidase inhibitor complex","type":"exact"},{"name":"serpin complex","type":"exact"}],"termid":"GO:0097180"}


id: PBO:0079781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP glucuronosyltransferase family 1 member A2, pseudogene","termid":"PBO:0079781"}


id: GO:0045147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the activation, by acetate, of the chemical reactions and pathways resulting in the breakdown of acetate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of acetate catabolic process","termid":"GO:0045734"},{"relation_name":"is_a","term_name":"regulation of response to acetate","termid":"GO:1901457"},{"relation_name":"regulates","term_name":"initiation of acetate catabolic process by acetate","termid":"GO:0045146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"regulation of initiation of acetate catabolic process by acetate","synonyms":[{"name":"regulation of initiation of acetate breakdown by acetate","type":"exact"},{"name":"regulation of initiation of acetate degradation by acetate","type":"exact"}],"termid":"GO:0045147"}


id: GO:0070840
data:
  {"annotated_genes":["SJAG_00594","SJAG_02651"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106347,106680],"is_not":false,"summary":null,"term":"GO:0070840"}]},"cv_name":"molecular_function","definition":"Binding to a dynein complex, a protein complex that contains two or three dynein heavy chains and several light chains, and has microtubule motor activity.","definition_xrefs":["GOC:BHF","GOC:mah","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00594":null,"SJAG_02651":null},"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":"dynein complex binding","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0045502"],"synonyms":[{"name":"dynein binding","type":"related"}],"termid":"GO:0070840","terms_by_termid":{"GO:0070840":null}}


id: PBO:0029325
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H2A_phosphorylation_at_rDNA","termid":"PBO:0029325"}


id: GO:0014888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which striated muscle adapts, with consequent modifications to structural and/or functional phenotypes, in response to a stimulus. Stimuli include contractile activity, loading conditions, substrate supply, and environmental factors. These adaptive events occur in both muscle fibers and associated structures (motoneurons and capillaries), and they involve alterations in regulatory mechanisms, contractile properties and metabolic capacities.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle adaptation","termid":"GO:0043500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"striated muscle adaptation","synonyms":[{"name":"striated muscle plasticity","type":"related"}],"termid":"GO:0014888"}


id: PBO:0036142
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_iron","termid":"PBO:0036142"}


id: PBO:0049633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 36","termid":"PBO:0049633"}


id: MOD:00997
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclohexyl ester","synonyms":[{"name":"OcHex","type":"exact"}],"termid":"MOD:00997"}


id: PBO:0082834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Constituent of 66S pre-ribosomal particles; has similarity to human translation initiation factor 6 (eIF6); may be involved in the biogenesis and or stability of 60S ribosomal subunits","termid":"PBO:0082834"}


id: PBO:0116806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLGAP1 antisense RNA 6","termid":"PBO:0116806"}


id: GO:0070651
data:
  {"annotated_genes":["SJAG_03728","SJAG_01191","SJAG_04321","SJAG_03507","SJAG_04283","SJAG_04084","SJAG_04006","SJAG_04824","SJAG_04153","SJAG_04818","SJAG_01818","SJAG_03179","SJAG_01521","SJAG_00854","SJAG_03745"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76229,94014,94847,97695,99021,99277,103875,106196,107064,108276,109269,109358,117285,117724,120166],"is_not":false,"summary":null,"term":"GO:0070651"}]},"cv_name":"biological_process","definition":"An rRNA catabolic process that results in the targeted detection and degradation of aberrant rRNAs contained within translationally defective ribosomes, thereby acting as a quality-control system.","definition_xrefs":["PMID:17188037","GOC:rn","GOC:mah","PMID:19390089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA catabolic process","termid":"GO:0016075"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00854":null,"SJAG_01191":null,"SJAG_01521":null,"SJAG_01818":null,"SJAG_03179":null,"SJAG_03507":null,"SJAG_03728":null,"SJAG_03745":null,"SJAG_04006":null,"SJAG_04084":null,"SJAG_04153":null,"SJAG_04283":null,"SJAG_04321":null,"SJAG_04818":null,"SJAG_04824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"nonfunctional rRNA decay","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"NRD","type":"related"}],"termid":"GO:0070651","terms_by_termid":{"GO:0070651":null}}


id: GO:0004917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-7 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:signaling","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"interleukin-7 receptor activity","synonyms":[{"name":"IL-7 receptor activity","type":"exact"},{"name":"IL-7R","type":"exact"}],"termid":"GO:0004917"}


id: PATO:0001073
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001073 relative impulse (obsolete PATO:0001073)","termid":"PATO:0001073"}


id: GO:0099136
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Development of a non-reproductive fruiting body formed by aggregation of cells with different genotypes.","definition_xrefs":["PMID:18272966"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chimeric colonial development","termid":"GO:0099135"}],"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":"chimeric non-reproductive fruiting body development","termid":"GO:0099136"}


id: PBO:0041457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C10orf71 antisense RNA 1","termid":"PBO:0041457"}


id: MOD:00985
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes a hydrogen atom of an L-tyrosine residue with a halogen atom.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"halogen containing residue","termid":"MOD:00694"},{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"halogenated tyrosine","synonyms":[{"name":"HalTyr","type":"exact"}],"termid":"MOD:00985"}


id: PBO:0087715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; general transcription factor involved in telomere maintenance","termid":"PBO:0087715"}


id: PBO:0090110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA(Ser) Um(44) 2'-O-methyltransferasetRNA Trm44","termid":"PBO:0090110"}


id: GO:1900212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mesenchymal cell apoptotic process involved in metanephros development.","definition_xrefs":["GOC:yaf","GOC:mtg_kidney_jan10","GOC:mtg_apoptosis","GOC:TermGenie","PMID:17314325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal cell apoptotic process involved in metanephros development","termid":"GO:1900211"},{"relation_name":"is_a","term_name":"negative regulation of apoptotic process involved in development","termid":"GO:1904746"},{"relation_name":"is_a","term_name":"negative regulation of mesenchymal cell apoptotic process","termid":"GO:2001054"},{"relation_name":"negatively_regulates","term_name":"mesenchymal cell apoptotic process involved in metanephros development","termid":"GO:1900200"}],"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 mesenchymal cell apoptotic process involved in metanephros development","synonyms":[{"name":"down regulation of mesenchymal cell apoptosis involved in metanephros development","type":"exact"},{"name":"down-regulation of mesenchymal cell apoptosis involved in metanephros development","type":"exact"},{"name":"downregulation of mesenchymal cell apoptosis involved in metanephros development","type":"exact"},{"name":"inhibition of mesenchymal cell apoptosis involved in metanephros development","type":"narrow"},{"name":"negative regulation of mesenchymal cell apoptosis involved in metanephros development","type":"narrow"}],"termid":"GO:1900212"}


id: PBO:0081674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 595","termid":"PBO:0081674"}


id: GO:0051796
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of timing of catagen, the regression phase of the hair cycle.","definition_xrefs":["GOC:pr","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hair follicle maturation","termid":"GO:0048817"},{"relation_name":"is_a","term_name":"regulation of timing of catagen","termid":"GO:0051794"},{"relation_name":"negatively_regulates","term_name":"catagen","termid":"GO:0042637"}],"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 timing of catagen","synonyms":[{"name":"down regulation of catagen","type":"related"},{"name":"down-regulation of catagen","type":"related"},{"name":"downregulation of catagen","type":"related"},{"name":"inhibition of catagen","type":"narrow"},{"name":"negative regulation of catagen","type":"related"}],"termid":"GO:0051796"}


id: GO:0048313
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The partitioning of Golgi apparatus between daughter cells at cell division.","definition_xrefs":["GOC:jid","PMID:12851069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi organization","termid":"GO:0007030"},{"relation_name":"is_a","term_name":"organelle inheritance","termid":"GO:0048308"}],"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":"Golgi inheritance","secondary_identifiers":["Reactome:R-HSA-162658"],"synonyms":[{"name":"Golgi apparatus inheritance","type":"exact"},{"name":"Golgi division","type":"exact"},{"name":"Golgi partitioning","type":"exact"}],"termid":"GO:0048313"}


id: PBO:0059629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MTCH2 pseudogene 1","termid":"PBO:0059629"}


id: PBO:0049236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate metabotropic receptor 7","termid":"PBO:0049236"}


id: MONDO:0009389
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hyperlysinemia","termid":"MONDO:0009388"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"hyperlysinemia due to defect in lysine transport into mitochondria","secondary_identifiers":["MESH:C565499","OMIM:238710","UMLS:C1855927","MEDGEN:341010","GARD:15183"],"synonyms":[{"name":"hyperlysinemia due to defect in lysine TRANSPORT into mitochondria","type":"related"}],"termid":"MONDO:0009389","xrefs":{"Monarch":{"xref_id":"0009389"}}}


id: FYECO:0000107
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which aminopyrimidine 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":"+ aminopyrimidine","termid":"FYECO:0000107"}


id: PBO:0049693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HAO2 intronic transcript 1","termid":"PBO:0049693"}


id: PBO:0054401
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 1797","termid":"PBO:0054401"}


id: GO:0010783
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the proboscis that are derived from the eye-antennal disc are generated and organized.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"eye-antennal disc morphogenesis","termid":"GO:0007455"},{"relation_name":"part_of","term_name":"proboscis morphogenesis","termid":"GO:0048734"}],"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":"proboscis morphogenesis, eye-antennal disc-derived","termid":"GO:0010783"}


id: PBO:0065699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purine rich element binding protein A","termid":"PBO:0065699"}


id: PBO:0043574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type IX alpha 2 chain","termid":"PBO:0043574"}


id: PR:O59855
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ssa2 gene.","definition_xrefs":["UniProtKB:O59855","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":"heat shock protein ssa2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1739.13","synonyms":[{"name":"Spom972h-ssa2","type":"exact"}],"termid":"PR:O59855"}


id: PBO:0004197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-2 adaptor complex subunit Aps2 (predicted)","termid":"PBO:0004197"}


id: PBO:0091022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mating-type transcription factor (Mc-like)","termid":"PBO:0091022"}


id: MONDO:0014912
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary periodic fever syndrome","termid":"MONDO:0017953"},{"relation_name":"is_a","term_name":"autoinflammation, panniculitis, and dermatosis syndrome","termid":"MONDO:0975955"}],"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":"autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive","secondary_identifiers":["OMIM:617099","Orphanet:500062","GARD:13198","DOID:0080163","MEDGEN:934581","SCTID:765435009","UMLS:C4310614"],"synonyms":[{"name":"AIPDS","type":"exact"},{"name":"AUTOINFLAMMATION, panniculitis, and dermatosis syndrome","type":"related"},{"name":"Autoinflammation, panniculitis, and dermatosis syndrome","type":"exact"},{"name":"ORAS","type":"exact"},{"name":"autoinflammation, panniculitis and dermatosis syndrome","type":"exact"},{"name":"otulin deficiency","type":"exact"},{"name":"otulin-related autoinflammatory syndrome","type":"exact"},{"name":"otulipenia","type":"exact"}],"termid":"MONDO:0014912","xrefs":{"Monarch":{"xref_id":"0014912"}}}


id: PBO:0068590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 41, pseudogene","termid":"PBO:0068590"}


id: GO:0160246
data:
  {"annotated_genes":["SJAG_00972"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[65695],"is_not":false,"summary":null,"term":"GO:0160246"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 oxidized [2Fe-2S]-[protein] + NADPH = 2 reduced [2Fe-2S]-[protein] + NADP+ + H+.","definition_xrefs":["RHEA:67716"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor","termid":"GO:0016731"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00972":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"NADPH-iron-sulfur [2Fe-2S] protein oxidoreductase activity","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:0160246","terms_by_termid":{"GO:0160246":null}}


id: MONDO:0001762
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tooth erosion, non-bacterial that involves the dentine.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tooth erosion, non-bacterial","termid":"MONDO:0002325"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dentine erosion","secondary_identifiers":["MEDGEN:1843465","DOID:13629","UMLS:C1456162","ICD9:521.32"],"synonyms":[{"name":"dentine tooth erosion, non-bacterial","type":"exact"},{"name":"tooth erosion, non-bacterial of dentine","type":"exact"}],"termid":"MONDO:0001762","xrefs":{"Monarch":{"xref_id":"0001762"}}}


id: PBO:0001624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF3c","termid":"PBO:0001624"}


id: PBO:0055244
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 2671","termid":"PBO:0055244"}


id: MONDO:1012412
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"type 2 polysaccharide storage myopathy, non-human animal","termid":"MONDO:1011801"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"type 2 polysaccharide storage myopathy, horse","secondary_identifiers":["OMIA:001537-9796"],"termid":"MONDO:1012412","xrefs":{"Monarch":{"xref_id":"1012412"}}}


id: PBO:0027187
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_actomyosin_contractile_ring_organization","termid":"PBO:0027187"}


id: PBO:0056180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAF bZIP transcription factor F","termid":"PBO:0056180"}


id: PBO:0067126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 172, pseudogene","termid":"PBO:0067126"}


id: PBO:0076653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T-box transcription factor 10","termid":"PBO:0076653"}


id: MONDO:0009593
data:
  {"annotated_genes":["SJAG_01216"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86886],"is_not":false,"summary":null,"term":"MONDO:0009593"}]},"cv_name":"mondo","definition":"Spondylometaphyseal dysplasia (SEMD), Sedaghatian type is a neonatal lethal form of spondylometaphyseal dysplasia characterized by severe metaphyseal chondrodysplasia, mild rhizomelic shortness of the upper limbs, and mild platyspondyly.","definition_xrefs":["Orphanet:93317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"},{"relation_name":"is_a","term_name":"inherited glutathione metabolism disease","termid":"MONDO:0040566"},{"relation_name":"is_a","term_name":"severe spondylodysplastic dysplasia","termid":"MONDO:0800080"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01216":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019241"}],"interesting_parent_ids":["MONDO:0019241","MONDO:0005066"],"is_obsolete":false,"name":"spondylometaphyseal dysplasia, Sedaghatian type","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:340816","MESH:C535798","DOID:0112298","GARD:4993","icd11.foundation:975738106","UMLS:C1855229","OMIM:250220"],"synonyms":[{"name":"SMDS","type":"related"},{"name":"Sedaghatian chondrodysplasia","type":"related"},{"name":"lethal metaphyseal dysplasia","type":"related"},{"name":"metaphyseal chondrodysplasia, congenital lethal","type":"related"},{"name":"spondylometaphyseal dysplasia Sedaghatian type","type":"related"},{"name":"spondylometaphyseal dysplasia, Sedaghatian type","type":"exact"}],"termid":"MONDO:0009593","terms_by_termid":{"MONDO:0009593":null},"xrefs":{"Monarch":{"xref_id":"0009593"}}}


id: GO:0061829
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Actin-based structures involved in establishing the blood-testis barrier of the Sertoli cell.","definition_xrefs":["PMID:22510523","PMID:20403871"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tubulobulbar complex","termid":"GO:0036284"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"basal tubulobulbar complex","synonyms":[{"name":"basal TBC","type":"exact"}],"termid":"GO:0061829"}


id: MONDO:0017001
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete X chromosome number anomaly with male phenotype (obsolete MONDO:0017001)","secondary_identifiers":["Orphanet:263720"],"termid":"MONDO:0017001","xrefs":{"Monarch":{"xref_id":"0017001"}}}


id: GO:0046969
data:
  {"annotated_genes":["SJAG_04186","SJAG_01075"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79035,116265],"is_not":false,"summary":null,"term":"GO:0046969"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H3 N6-acetyl-L-lysine (position 9) + NAD+ + H2O = histone H3 L-lysine (position 9) + 2''-O-acetyl-ADP-D-ribose + nicotinamide. This reaction transfers an acetyl group attached to a lysine residue in H3K9 to NAD, producing nicotinamide.","definition_xrefs":["PMID:28450737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone deacetylase activity, NAD-dependent","termid":"GO:0017136"},{"relation_name":"is_a","term_name":"histone H3K deacetylase activity","termid":"GO:0141050"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01075":null,"SJAG_04186":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0033558"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016746","GO:0140096","GO:0003824","GO:0003674","GO:0019213","GO:0033558","GO:0016740"],"is_obsolete":false,"name":"histone H3K9 deacetylase activity, NAD-dependent","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9604829"],"synonyms":[{"name":"NAD-dependent H3-K9 histone deacetylase activity","type":"exact"},{"name":"NAD-dependent histone H3K9 deacetylase activity","type":"exact"},{"name":"NAD-dependent histone deacetylase activity (H3-K9 specific)","type":"exact"}],"termid":"GO:0046969","terms_by_termid":{"GO:0046969":null}}


id: GO:0019411
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The metabolic process in which ferrous ions (Fe2+) are oxidized to ferric ions (Fe3+) to generate energy, coupled to the reduction of carbon dioxide.","definition_xrefs":["ISBN:3131084111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aerobic respiration","termid":"GO:0009060"},{"relation_name":"is_a","term_name":"energy derivation by oxidation of reduced inorganic compounds","termid":"GO:0015975"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"aerobic respiration, using ferrous ions as electron donor","termid":"GO:0019411"}


id: PBO:0029014
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_centromeric_outer_repeat_transcript-derived_siRNA_level","termid":"PBO:0029014"}


id: PBO:0049609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 12","termid":"PBO:0049609"}


id: PBO:0028843
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_heterochromatin_assembly","termid":"PBO:0028843"}


id: GO:0110083
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein localization to cell division site involved in mitotic actomyosin contractile ring assembly.","definition_xrefs":["GOC:vw","PMID:29343550"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","termid":"GO:0110082"},{"relation_name":"is_a","term_name":"positive regulation of protein localization","termid":"GO:1903829"},{"relation_name":"positively_regulates","term_name":"protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","termid":"GO:1903476"}],"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 protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","termid":"GO:0110083"}


id: MONDO:0003664
data:
  {"annotated_genes":["SJAG_00988","SJAG_00605","SJAG_02009","SJAG_01077","SJAG_05283","SJAG_00846","SJAG_02796","SJAG_03153","SJAG_04192","SJAG_04495","SJAG_04881","SJAG_03497","SJAG_04334","SJAG_02539","SJAG_00930","SJAG_01351","SJAG_01183","SJAG_00839","SJAG_01162","SJAG_02297","SJAG_04731"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010480"},{"annotations":[87191,87190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009134"},{"annotations":[87234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007109"},{"annotations":[88134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008494"},{"annotations":[87195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009902"},{"annotations":[87038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012204"},{"annotations":[87643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009259"},{"annotations":[87953],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009284"},{"annotations":[87414],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009295"},{"annotations":[88834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009113"},{"annotations":[87925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013275"},{"annotations":[88615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019531"},{"annotations":[89099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859172"},{"annotations":[87205],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012981"},{"annotations":[88207,88208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009340"},{"annotations":[88146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008493"},{"annotations":[87184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012992"},{"annotations":[88664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010438"},{"annotations":[87697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014166"},{"annotations":[87335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009950"},{"annotations":[86936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012700"},{"annotations":[88967],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019107"},{"annotations":[87376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008165"},{"annotations":[87527],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014221"}]},"cv_name":"mondo","definition":"Anemia resulting from the premature destruction of the peripheral blood red cells. It may be congenital or it may be caused by infections, medications, or malignancies.","definition_xrefs":["NCIT:C34376"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normocytic anemia","termid":"MONDO:0004139"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00605":null,"SJAG_00839":null,"SJAG_00846":null,"SJAG_00930":null,"SJAG_00988":null,"SJAG_01077":null,"SJAG_01162":null,"SJAG_01183":null,"SJAG_01351":null,"SJAG_02009":null,"SJAG_02297":null,"SJAG_02539":null,"SJAG_02796":null,"SJAG_03153":null,"SJAG_03497":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_04731":null,"SJAG_04881":null,"SJAG_05283":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"hemolytic anemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2200636","DOID:583","MEDGEN:1916","SCTID:61261009","UMLS:C0002878","MESH:D000743","ICD10CM:D55-D59"],"synonyms":[{"name":"anaemia hemolytic","type":"exact"},{"name":"anemia hemolytic","type":"exact"},{"name":"anemia, hemolytic","type":"exact"},{"name":"hemolytic anemia","type":"exact"}],"termid":"MONDO:0003664","terms_by_termid":{"MONDO:0007109":null,"MONDO:0008165":null,"MONDO:0008493":null,"MONDO:0008494":null,"MONDO:0009113":null,"MONDO:0009134":null,"MONDO:0009259":null,"MONDO:0009284":null,"MONDO:0009295":null,"MONDO:0009340":null,"MONDO:0009902":null,"MONDO:0009950":null,"MONDO:0010438":null,"MONDO:0010480":null,"MONDO:0012204":null,"MONDO:0012700":null,"MONDO:0012981":null,"MONDO:0012992":null,"MONDO:0013275":null,"MONDO:0014166":null,"MONDO:0014221":null,"MONDO:0019107":null,"MONDO:0019531":null,"MONDO:0859172":null},"xrefs":{"Monarch":{"xref_id":"0003664"}}}


id: GO:1900141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of oligodendrocyte apoptotic process.","definition_xrefs":["GOC:yaf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glial cell apoptotic process","termid":"GO:0034350"},{"relation_name":"regulates","term_name":"oligodendrocyte apoptotic process","termid":"GO:0097252"}],"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 oligodendrocyte apoptotic process","synonyms":[{"name":"regulation of oligodendrocyte apoptosis","type":"narrow"}],"termid":"GO:1900141"}


id: PBO:0116580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane and mitochondrial outer membrane, implicated in cell integrity signaling, conserved fungal protein","termid":"PBO:0116580"}


id: PBO:0070086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear variant sequence with SNRPE pseudogene sequence","termid":"PBO:0070086"}


id: PBO:0046212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin C pseudogene 5","termid":"PBO:0046212"}


id: GO:0032121
data:
  {"annotated_genes":["SJAG_01777","SJAG_05260","SJAG_03287","SJAG_05196","SJAG_03092"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89162,91538,101712,104617,106910],"is_not":false,"summary":null,"term":"GO:0032121"}]},"cv_name":"biological_process","definition":"The meiotic cell cycle process in which physical connections are formed between telomeric heterochromatin and the spindle pole body, facilitating bouquet formation.","definition_xrefs":["PMID:16615890","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule-based process","termid":"GO:0007017"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"meiotic telomere clustering","termid":"GO:0045141"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01777":null,"SJAG_03092":null,"SJAG_03287":null,"SJAG_05196":null,"SJAG_05260":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0140013","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"meiotic attachment of telomeric heterochromatin to spindle pole body","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"attachment of telomeres to spindle pole body","type":"broad"},{"name":"attachment of telomeric chromatin to spindle pole body","type":"broad"}],"termid":"GO:0032121","terms_by_termid":{"GO:0032121":null}}


id: PBO:0084286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Integral membrane protein required for V-ATPase function; not an actual component of the vacuolar H+-ATPase (V-ATPase) complex; functions in the assembly of the V-ATPase; localized to the endoplasmic reticulum (ER); involved in methionine restriction extension of chronological lifespan in an autophagy-dependent manner","termid":"PBO:0084286"}


id: PBO:0062192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily R member 1 pseudogene","termid":"PBO:0062192"}


id: PBO:0052864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 5-7","termid":"PBO:0052864"}


id: PBO:0086829
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; YPL034W is not essential gene","termid":"PBO:0086829"}


id: PBO:0041589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CA3 antisense RNA 1","termid":"PBO:0041589"}


id: PBO:0078425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon GCC) 2-6","termid":"PBO:0078425"}


id: PBO:0055969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRR binding FLII interacting protein 1 pseudogene 1","termid":"PBO:0055969"}


id: PBO:0068018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 323","termid":"PBO:0068018"}


id: PBO:0038942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alcohol dehydrogenase 6 (class V)","termid":"PBO:0038942"}


id: PBO:0116754
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 E1","termid":"PBO:0116754"}


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


id: PBO:0047383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 17","termid":"PBO:0047383"}


id: GO:0052708
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 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 metabolic process","termid":"GO:0006577"},{"relation_name":"is_a","term_name":"L-amino acid metabolic process","termid":"GO:0170033"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid metabolic process","termid":"GO:0170041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolic process","synonyms":[{"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolism","type":"exact"},{"name":"hercynine metabolic process","type":"exact"},{"name":"hercynine metabolism","type":"exact"},{"name":"histidine betaine metabolic process","type":"exact"},{"name":"histidine betaine metabolism","type":"exact"}],"termid":"GO:0052708"}


id: PBO:0071482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 23","termid":"PBO:0071482"}


id: PBO:0003169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin ligase complex subunit, involved in proteasome-dependent catabolite inactivation of FBPase (predicted)","termid":"PBO:0003169"}


id: PBO:0080153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"versican","termid":"PBO:0080153"}


id: FYPO:0001471
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing tacrolimus, when the cell is subject to salt stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal growth during cellular response to salt stress","termid":"FYPO:0001037"},{"relation_name":"is_a","term_name":"normal growth on tacrolimus during osmotic stress","termid":"FYPO:0001472"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0000003","FYPO:0002058","FYPO:0002057","FYPO:0000139","FYPO:0000257"],"is_obsolete":false,"name":"normal growth on tacrolimus during salt stress","synonyms":[{"name":"normal cell population growth in presence of tacrolimus during salt stress","type":"exact"},{"name":"normal cell population growth on FK506 during salt stress","type":"exact"},{"name":"normal cell population growth on tacrolimus during salt stress","type":"exact"},{"name":"normal cellular response to salt stress and tacrolimus","type":"related"},{"name":"normal cellular response to tacrolimus and salt stress","type":"related"},{"name":"normal cellular response to tacrolimus during salt stress","type":"related"},{"name":"normal vegetative cell population growth on tacrolimus during salt stress","type":"exact"}],"termid":"FYPO:0001471"}


id: PBO:0063949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIN2 (TERF1) interacting telomerase inhibitor 1","termid":"PBO:0063949"}


id: PBO:0058244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4531","termid":"PBO:0058244"}


id: PBO:0056032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukotriene A4 hydrolase","termid":"PBO:0056032"}


id: PBO:0075429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm adhesion molecule 1","termid":"PBO:0075429"}


id: PR:O14443
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GPN-loop GTPase 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR21231:SF4","OMA:SCHPO02232","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":"GPN-loop GTPase 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.12c","secondary_identifiers":["UniProtKB:O14443"],"synonyms":[{"name":"Spom972h-GPN3","type":"exact"},{"name":"factor of eukaryotic transcription 5 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14443"}


id: GO:0004173
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: Ecdysone + palmitoyl-CoA = CoA + ecdysone palmitate.","definition_xrefs":["EC:2.3.1.139","RHEA:15217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016746","GO:0003824"],"is_obsolete":false,"name":"ecdysone O-acyltransferase activity","secondary_identifiers":["MetaCyc:ECDYSONE-O-ACYLTRANSFERASE-RXN","KEGG_REACTION:R02375"],"synonyms":[{"name":"acyl-CoA:ecdysone acyltransferase activity","type":"related"},{"name":"fatty acyl-CoA:ecdysone acyltransferase activity","type":"related"},{"name":"palmitoyl-CoA:ecdysone palmitoyltransferase activity","type":"related"}],"termid":"GO:0004173"}


id: GO:0097348
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a host cell endocytic vesicle.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell cytoplasmic vesicle membrane","termid":"GO:0044162"}],"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 endocytic vesicle membrane","termid":"GO:0097348"}


id: PBO:0050508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox C8","termid":"PBO:0050508"}


id: GO:0061438
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the renal system vasculature is generated and organized. Morphogenesis pertains to the creation of form.","definition_xrefs":["PMID:11891195","GOC:dph","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"renal system vasculature development","termid":"GO:0061437"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal system vasculature morphogenesis","termid":"GO:0061438"}


id: PBO:0063844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol 4-kinase beta","termid":"PBO:0063844"}


id: GO:0004167
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-dopachrome = 5,6-dihydroxyindole-2-carboxylate.","definition_xrefs":["EC:5.3.3.12","RHEA:13041"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, transposing C=C bonds","termid":"GO:0016863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"dopachrome isomerase activity","secondary_identifiers":["MetaCyc:DOPACHROME-DELTA-ISOMERASE-RXN","GO:0048059","KEGG_REACTION:R03673"],"synonyms":[{"name":"DCF activity","type":"related"},{"name":"DCT activity","type":"related"},{"name":"L-dopachrome isomerase activity","type":"related"},{"name":"L-dopachrome keto-enol isomerase activity","type":"related"},{"name":"L-dopachrome-methyl ester tautomerase activity","type":"related"},{"name":"TRP activity","type":"related"},{"name":"TRP-1","type":"related"},{"name":"TRP-2","type":"related"},{"name":"TRP2","type":"related"},{"name":"dopachrome Delta(7),Delta(2)-isomerase activity","type":"related"},{"name":"dopachrome conversion activity","type":"broad"},{"name":"dopachrome conversion factor activity","type":"broad"},{"name":"dopachrome delta-isomerase activity","type":"exact"},{"name":"dopachrome delta7,Delta2-isomerase activity","type":"related"},{"name":"dopachrome keto-enol isomerase activity","type":"related"},{"name":"dopachrome oxidoreductase activity","type":"related"},{"name":"dopachrome rearranging enzyme activity","type":"related"},{"name":"dopachrome tautomerase activity","type":"related"},{"name":"dopachrome-rearranging enzyme","type":"related"},{"name":"tryosinase-related protein-2","type":"related"},{"name":"tyrosinase-related protein 2 activity","type":"related"}],"termid":"GO:0004167"}


id: PBO:0078995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (anticodon AGT) 2-2","termid":"PBO:0078995"}


id: MONDO:0020751
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited orthostatic hypotension","termid":"MONDO:0021272"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orthostatic hypotension 2","secondary_identifiers":["UMLS:C4748569","MEDGEN:1648282","OMIM:618182"],"termid":"MONDO:0020751","xrefs":{"Monarch":{"xref_id":"0020751"}}}


id: GO:0031539
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chemical reactions and pathways involving anthocyanins.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of metabolic process","termid":"GO:0009893"},{"relation_name":"is_a","term_name":"regulation of anthocyanin metabolic process","termid":"GO:0031537"},{"relation_name":"positively_regulates","term_name":"anthocyanin-containing compound metabolic process","termid":"GO:0046283"}],"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 anthocyanin metabolic process","synonyms":[{"name":"activation of anthocyanin metabolic process","type":"narrow"},{"name":"positive regulation of anthocyanin metabolism","type":"exact"},{"name":"stimulation of anthocyanin metabolic process","type":"narrow"},{"name":"up regulation of anthocyanin metabolic process","type":"exact"},{"name":"up-regulation of anthocyanin metabolic process","type":"exact"},{"name":"upregulation of anthocyanin metabolic process","type":"exact"}],"termid":"GO:0031539"}


id: GO:0045433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process during wing vibration where the male insect produces a species-specific acoustic signal called a love song.","definition_xrefs":["GOC:mtg_sensu","PMID:11092827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male courtship behavior","termid":"GO:0008049"},{"relation_name":"part_of","term_name":"male courtship behavior, veined wing vibration","termid":"GO:0016545"}],"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":"male courtship behavior, veined wing generated song production","synonyms":[{"name":"male courtship behavior, song production","type":"broad"},{"name":"male courtship behaviour, song production","type":"broad"},{"name":"male courtship behaviour, veined wing generated song production","type":"exact"}],"termid":"GO:0045433"}


id: GO:0000421
data:
  {"annotated_genes":["SJAG_02414","SJAG_06309"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72202,73762],"is_not":false,"summary":null,"term":"GO:0000421"}]},"cv_name":"cellular_component","definition":"The lipid bilayer surrounding an autophagosome, a double-membrane-bounded vesicle in which endogenous cellular material is sequestered.","definition_xrefs":["GOC:autophagy","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuolar membrane","termid":"GO:0005774"},{"relation_name":"part_of","term_name":"autophagosome","termid":"GO:0005776"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02414":null,"SJAG_06309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005773"],"is_obsolete":false,"name":"autophagosome membrane","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"autophagic vacuole membrane","type":"exact"}],"termid":"GO:0000421","terms_by_termid":{"GO:0000421":null}}


id: FYPO:0000934
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 microtubule cytoskeleton does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000931"},{"relation_name":"is_a","term_name":"abolished protein localization during vegetative growth","termid":"FYPO:0001179"},{"relation_name":"is_a","term_name":"abolished protein localization to microtubule cytoskeleton","termid":"FYPO:0004091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to microtubule cytoskeleton during vegetative growth","synonyms":[{"name":"abolished protein localisation to microtubule cytoskeleton during vegetative growth","type":"exact"},{"name":"abolished protein localization to microtubule cytoskeleton during mitotic cell cycle","type":"related"},{"name":"protein absent from microtubule cytoskeleton during vegetative growth","type":"related"},{"name":"protein localization to microtubule cytoskeleton abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0000934"}


id: MONDO:0017673
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A focal palmoplantar keratoderma that is not part of a larger syndrome.","definition_xrefs":["MONDO:patterns/isolated"],"gene_count":0,"genotype_count":0,"name":"obsolete isolated focal palmoplantar keratoderma (obsolete MONDO:0017673)","secondary_identifiers":["Orphanet:307846"],"synonyms":[{"name":"isolated focal PPK","type":"exact"},{"name":"isolated focal keratosis palmoplantaris","type":"exact"},{"name":"isolated focal palmoplantar hyperkeratosis","type":"exact"},{"name":"nonsyndromic focal palmoplantar keratoderma","type":"exact"}],"termid":"MONDO:0017673","xrefs":{"Monarch":{"xref_id":"0017673"}}}


id: MONDO:0006858
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the mouth.","direct_ancestors":[{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mouth disorder","secondary_identifiers":["DOID:403","ICD9:528.9","MEDGEN:6448","UMLS:C0026636","EFO:1001047","NCIT:C3240","SCTID:118938008","MESH:D009059"],"synonyms":[{"name":"disease of mouth","type":"exact"},{"name":"disease or disorder of mouth","type":"exact"},{"name":"disorder of mouth","type":"exact"},{"name":"mouth disease","type":"exact"},{"name":"mouth disease or disorder","type":"exact"},{"name":"oral disease","type":"exact"},{"name":"oral disorder","type":"exact"}],"termid":"MONDO:0006858","xrefs":{"Monarch":{"xref_id":"0006858"}}}


id: GO:0030388
data:
  {"annotated_genes":["SJAG_00605"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79528],"is_not":false,"summary":null,"term":"GO:0030388"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving fructose 1,6-bisphosphate, also known as FBP. The D enantiomer is a metabolic intermediate in glycolysis and gluconeogenesis.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"},{"relation_name":"is_a","term_name":"organophosphate metabolic process","termid":"GO:0019637"},{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00605":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"fructose 1,6-bisphosphate metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"fructose 1,6-bisphosphate metabolism","type":"exact"}],"termid":"GO:0030388","terms_by_termid":{"GO:0030388":null}}


id: PBO:0017483
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-causal_relation_between_processes","termid":"PBO:0017483"}


id: MONDO:0020488
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atypical progressive supranuclear palsy (atypical PSP) is a group of clinical syndromes associated with underlying PSP-tau pathology, that do not conform to the classic presentation of PSP (Richardson syndrome), a rare late-onset neurodegenerative disease. The group comprises PSP-Parkinsonism (PSP-P), PSP-Pure akinesia with gait freezing (PSP-PAGF), PSP-corticobasal syndrome (PSP-CBS) and PSP-progressive non fluent aphasia (PSP-PNFA).","definition_xrefs":["Orphanet:99750"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive supranuclear palsy","termid":"MONDO:0019037"}],"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":"atypical progressive supranuclear palsy syndrome","secondary_identifiers":["UMLS:C5548371","GARD:4507","MEDGEN:1779597"],"synonyms":[{"name":"atypical PSP syndrome","type":"exact"}],"termid":"MONDO:0020488","xrefs":{"Monarch":{"xref_id":"0020488"}}}


id: GO:0046097
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of deoxyuridine, 2-deoxyribosyluracil, one of the four major nucleosides of DNA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyuridine metabolic process","termid":"GO:0046096"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside biosynthetic process","termid":"GO:0046126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"deoxyuridine biosynthetic process","synonyms":[{"name":"deoxyuridine anabolism","type":"exact"},{"name":"deoxyuridine biosynthesis","type":"exact"},{"name":"deoxyuridine formation","type":"exact"},{"name":"deoxyuridine synthesis","type":"exact"}],"termid":"GO:0046097"}


id: PBO:0080882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YPEL5 pseudogene 2","termid":"PBO:0080882"}


id: GO:0022036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a rhombomere cell.","definition_xrefs":["GO_REF:0000021","GOC:jid","GOC:cls","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"rhombomere development","termid":"GO:0021546"}],"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":"rhombomere cell differentiation","termid":"GO:0022036"}


id: GO:0048518
data:
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id: PBO:0001555
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id: GO:0120235
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id: PBO:0000942
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id: PBO:0111816
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id: MONDO:0002255
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id: PBO:0046681
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id: PBO:0001743
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id: GO:0042376
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id: PATO:0000949
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id: MONDO:0012160
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id: MOD:00836
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id: MONDO:0008189
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign neoplasm that arises in the area of the nipple. Clinically, it usually presents as a tender erythematous crusting lesion with hardening of the nipple. Morphologically, there is proliferation of ducts lined with epithelial and myoepithelial cells and focal erosion of the epidermis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papillomatosis, florid, of nipple","secondary_identifiers":["OMIM:167950","SCTID:237467005","UMLS:C1868647","MESH:C537167","NCIT:C4383","MEDGEN:401492"],"synonyms":[{"name":"erosive adenomatosis of nipple","type":"exact"},{"name":"erosive adenomatosis of the nipple","type":"related"},{"name":"erosive nipple adenomatosis","type":"exact"},{"name":"florid papillomatosis","type":"related"},{"name":"florid papillomatosis of the nipple","type":"related"},{"name":"papillomatosis florid of nipple","type":"related"},{"name":"papillomatosis, florid, of nipple","type":"exact"}],"termid":"MONDO:0008189","xrefs":{"Monarch":{"xref_id":"0008189"}}}


id: FYPO:0005084
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at ribosomal RNA (rRNA) genes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:21151114","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin at ncRNA gene","termid":"FYPO:0005083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal protein localization to chromatin at rRNA gene","synonyms":[{"name":"normal protein localisation to chromatin at rRNA gene","type":"exact"},{"name":"normal protein localization to chromatin at rDNA","type":"exact"},{"name":"normal protein localization to chromatin at rRNA gene during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at rRNA gene during vegetative growth","type":"exact"},{"name":"normal protein localization to chromatin at ribosomal DNA","type":"exact"}],"termid":"FYPO:0005084"}


id: PBO:0051345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2D-28","termid":"PBO:0051345"}


id: PBO:0117427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZDHHC20 pseudogene 2","termid":"PBO:0117427"}


id: GO:0042446
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of any hormone, naturally occurring substances secreted by specialized cells that affects the metabolism or behavior of other cells possessing functional receptors for the hormone.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"hormone metabolic process","termid":"GO:0042445"}],"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":"hormone biosynthetic process","synonyms":[{"name":"hormone anabolism","type":"exact"},{"name":"hormone biosynthesis","type":"exact"},{"name":"hormone formation","type":"exact"},{"name":"hormone synthesis","type":"exact"}],"termid":"GO:0042446"}


id: PBO:0071565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 31","termid":"PBO:0071565"}


id: PBO:0061513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSA2 pseudogene 3","termid":"PBO:0061513"}


id: PBO:0059963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 8","termid":"PBO:0059963"}


id: FYPO:0001677
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the medial cortex is increased in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to medial cortex during vegetative growth","termid":"FYPO:0000731"},{"relation_name":"is_a","term_name":"increased protein localization to cell division site","termid":"FYPO:0004655"},{"relation_name":"is_a","term_name":"increased protein localization to cell cortex during vegetative growth","termid":"FYPO:0009059"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"increased protein localization to medial cortex during vegetative growth","synonyms":[{"name":"increased protein localisation to medial cortex during vegetative growth","type":"exact"},{"name":"increased protein localization to medial cortex during mitotic cell cycle","type":"related"},{"name":"increased protein localization to medial ring during vegetative growth","type":"exact"}],"termid":"FYPO:0001677"}


id: PBO:0091633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADP-dependent aldo/keto reductase, unknown biological role, implicated in cellular detoxification","termid":"PBO:0091633"}


id: GO:0097691
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Small membrane vesicle (< 1 um) that buds off a prokaryotic cell plasma membrane, able to carry proteins, phospholipids, lipopolysaccharides, nucleic acids, viruses, and more. Important in intercellular communication and pathogenesis; can exist within host cells.","definition_xrefs":["GOC:aa","PMID:25704309"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular vesicle","termid":"GO:1903561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005576","GO:0005575"],"is_obsolete":false,"name":"bacterial extracellular vesicle","termid":"GO:0097691"}


id: PR:O60109
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pho8 gene.","definition_xrefs":["UniProtKB:O60109","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":"alkaline phosphatase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC14F5.13c","synonyms":[{"name":"Spom972h-pho8","type":"exact"}],"termid":"PR:O60109"}


id: MONDO:0014401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tall stature-scoliosis-macrodactyly of the great toes syndrome is a rare, genetic, overgrowth or tall stature syndrome with skeletal involvement characterized by early and proportional overgrowth, osteopenia, lumbar scoliosis, arachnodactyly of the hands and feet, macrodactyly of the hallux, coxa valga with epiphyseal dysplasia of the femoral capital epiphyses and susceptibility to slipped capital femoral epiphysis.","definition_xrefs":["Orphanet:329191"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tall stature-scoliosis-macrodactyly of the great toes syndrome","secondary_identifiers":["DOID:0070316","MEDGEN:863127","UMLS:C4014690","OMIM:615923","GARD:17495"],"synonyms":[{"name":"ECDM","type":"related"},{"name":"Miura type epiphyseal chondrodysplasia","type":"related"},{"name":"epiphyseal chondrodysplasia, MIURA type","type":"related"},{"name":"tall stature-scoliosis-macrodactyly of the halluces syndrome","type":"exact"}],"termid":"MONDO:0014401","xrefs":{"Monarch":{"xref_id":"0014401"}}}


id: GO:0070884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the calcineurin-NFAT signaling cascade.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of calcineurin-mediated signaling","termid":"GO:0106056"},{"relation_name":"regulates","term_name":"calcineurin-NFAT signaling cascade","termid":"GO:0033173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of calcineurin-NFAT signaling cascade","secondary_identifiers":["GO:0051532","GO:0051531"],"synonyms":[{"name":"NFAT protein import into nucleus","type":"narrow"},{"name":"regulation of NFAT protein import into nucleus","type":"narrow"},{"name":"regulation of calcineurin-NFAT signaling pathway","type":"related"},{"name":"regulation of calcineurin-NFAT signalling cascade","type":"exact"}],"termid":"GO:0070884"}


id: MONDO:0001023
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mature B- or T- cell leukemia with progressive clinical course. It is characterized by the presence of medium-sized lymphocytes with visible nucleoli (prolymphocytes) in the peripheral blood, bone marrow, and spleen.","definition_xrefs":["NCIT:C3181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic leukemia","termid":"MONDO:0001014"},{"relation_name":"is_a","term_name":"acute lymphoblastic leukemia","termid":"MONDO:0004967"}],"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":"prolymphocytic leukemia","secondary_identifiers":["MESH:D015463","DOID:1039","ICD9:204.80","UMLS:C0023486","SCTID:110006004","GARD:11965","ICDO:9832/3","MEDGEN:6062"],"synonyms":[{"name":"PLL","type":"exact"},{"name":"prolymphocytic leukaemia (B or T)","type":"exact"},{"name":"prolymphocytic leukaemia (B or T-cell)","type":"exact"},{"name":"prolymphocytic leukemia","type":"exact"},{"name":"prolymphocytic leukemia (B or T)","type":"exact"},{"name":"prolymphocytic leukemia (B or T-cell)","type":"exact"}],"termid":"MONDO:0001023","xrefs":{"Monarch":{"xref_id":"0001023"}}}


id: FYPO:0004667
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cohesion between sister chromatids is normal (i.e. indistinguishable from wild type) at the centromeric regions during meiosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal meiotic sister chromatid cohesion","termid":"FYPO:0002094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal meiotic sister chromatid cohesion at centromere","synonyms":[{"name":"normal meiotic sister chromatid cohesion, centromeric","type":"exact"},{"name":"normal sister chromatid cohesion at centromere during meiosis","type":"exact"}],"termid":"FYPO:0004667"}


id: PBO:0011116
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dynein LIc","termid":"PBO:0011116"}


id: GO:0015919
data:
  {"annotated_genes":["SJAG_05315","SJAG_02797","SJAG_00702","SJAG_02997","SJAG_03324","SJAG_04857","SJAG_04763","SJAG_00891","SJAG_02693","SJAG_02619","SJAG_04428","SJAG_02034","SJAG_00326","SJAG_03781","SJAG_05950","SJAG_03440","SJAG_01165"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113223,71822,72335,75002,73732,98256,81360,104057],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016558"},{"annotations":[72360,75394,63370],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016560"},{"annotations":[65222,119156,100354,117140],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016562"},{"annotations":[97210,92196,113224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045046"}]},"cv_name":"biological_process","definition":"The directed movement of substances to, from or across the peroxisomal membrane.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisomal transport","termid":"GO:0043574"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null,"SJAG_00891":null,"SJAG_01165":null,"SJAG_02034":null,"SJAG_02619":null,"SJAG_02693":null,"SJAG_02797":null,"SJAG_02997":null,"SJAG_03324":null,"SJAG_03440":null,"SJAG_03781":null,"SJAG_04428":null,"SJAG_04763":null,"SJAG_04857":null,"SJAG_05315":null,"SJAG_05950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"peroxisomal membrane transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0015919","terms_by_termid":{"GO:0016558":null,"GO:0016560":null,"GO:0016562":null,"GO:0045046":null}}


id: PBO:0069681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 958, pseudogene","termid":"PBO:0069681"}


id: PBO:0029529
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_alpha-glucanase","termid":"PBO:0029529"}


id: MONDO:0024429
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorienting neuropsychological condition that affects perception. People experience size distortion such as micropsia, macropsia, pelopsia, or teleopsia. Size distortion may occur of other sensory modalities.","definition_xrefs":["Wikipedia:Alice_in_Wonderland_syndrome"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"vision disorder","termid":"MONDO:0021084"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alice in Wonderland syndrome","secondary_identifiers":["MESH:D062026","MEDGEN:473310","NCIT:C116362","UMLS:C0854348"],"termid":"MONDO:0024429","xrefs":{"Monarch":{"xref_id":"0024429"}}}


id: PBO:0069757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1040, pseudogene","termid":"PBO:0069757"}


id: PBO:0084932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA export factor; required for biogenesis of the small ribosomal subunit; component of TREX-2 complex (Sac3p-Thp1p-Sus1p-Cdc31p) involved in transcription elongation and mRNA export from the nucleus; involved in post-transcriptional tethering of active genes to the nuclear periphery and to non-nascent mRNP; similar to the human germinal center-associated nuclear protein (GANP)","termid":"PBO:0084932"}


id: GO:0030391
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of fructosamine, a fructose molecule containing an amino group in place of a hydroxyl group.","definition_xrefs":["GOC:jl","ISBN:0192801023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fructosamine metabolic process","termid":"GO:0030389"},{"relation_name":"is_a","term_name":"amino sugar biosynthetic process","termid":"GO:0046349"}],"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":"fructosamine biosynthetic process","synonyms":[{"name":"fructosamine anabolism","type":"exact"},{"name":"fructosamine biosynthesis","type":"exact"},{"name":"fructosamine formation","type":"exact"},{"name":"fructosamine synthesis","type":"exact"}],"termid":"GO:0030391"}


id: PBO:0025422
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino acid metabolism disorders","termid":"PBO:0025422"}


id: PBO:0052145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KCNIP1 overlapping transcript 1","termid":"PBO:0052145"}


id: PBO:0068740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U5B small nuclear 3, pseudogene","termid":"PBO:0068740"}


id: GO:0106105
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-alanyl-tRNA(Thr) + H2O = tRNA(Thr) + L-alanine + H+.","definition_xrefs":["RHEA:17793","PMID:29410408"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyl-tRNA deacylase activity","termid":"GO:0002161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0140098","GO:0140101"],"is_obsolete":false,"name":"Ala-tRNA(Thr) deacylase activity","synonyms":[{"name":"L-alanyl-tRNA(Thr) deacylase","type":"exact"}],"termid":"GO:0106105"}


id: PBO:0073293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 14 pseudogene 15","termid":"PBO:0073293"}


id: FYPO:0001724
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of GTP binding by a gene product (usually a protein) in a mutant is increased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal GTP binding","termid":"FYPO:0001528"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"increased GTP binding","termid":"FYPO:0001724"}


id: PBO:0110027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACCSL pseudogene 1","termid":"PBO:0110027"}


id: GO:2000819
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of nucleotide-excision repair.","definition_xrefs":["GOC:jp","PMID:18836076"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA repair","termid":"GO:0006282"},{"relation_name":"regulates","term_name":"nucleotide-excision repair","termid":"GO:0006289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006281"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006281","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"regulation of nucleotide-excision repair","synonyms":[{"name":"regulation of NER","type":"exact"},{"name":"regulation of interstrand crosslink repair","type":"related"},{"name":"regulation of intrastrand cross-link repair","type":"related"},{"name":"regulation of pyrimidine-dimer repair, DNA damage excision","type":"exact"}],"termid":"GO:2000819"}


id: PBO:0046060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit J","termid":"PBO:0046060"}


id: PBO:0047970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FREM2 antisense RNA 1","termid":"PBO:0047970"}


id: PBO:0076992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THAP7 antisense RNA 1","termid":"PBO:0076992"}


id: FYPO:0007372
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of chlorpromazine than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002682","FYPO:0000139","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"resistance to chlorpromazine","synonyms":[{"name":"resistance to chlorpromazine during mitotic cell cycle","type":"related"},{"name":"resistance to chlorpromazine during vegetative growth","type":"exact"},{"name":"resistant to chlorpromazine","type":"exact"}],"termid":"FYPO:0007372"}


id: FYPO:0003545
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the duration of mitotic cell cycle arrest or delay due to regulation by the DNA replication checkpoint is greater than normal. The DNA replication checkpoint normally prevents the initiation of mitosis until DNA replication is complete.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle DNA replication checkpoint","termid":"FYPO:0000173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0005447","FYPO:0000298","FYPO:0001320"],"is_obsolete":false,"name":"increased duration of mitotic cell cycle DNA replication checkpoint","synonyms":[{"name":"increased duration of DNA replication checkpoint","type":"broad"},{"name":"increased duration of mitotic cell cycle DNA replication checkpoint activation","type":"exact"},{"name":"mitotic cell cycle DNA replication checkpoint activated","type":"related"},{"name":"prolonged mitotic cell cycle DNA replication checkpoint","type":"exact"}],"termid":"FYPO:0003545"}


id: PBO:0046296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EMSY transcriptional repressor, BRCA2 interacting","termid":"PBO:0046296"}


id: GO:1904389
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a rod bipolar cell.","definition_xrefs":["GO_REF:0000086","GOC:TermGenie","PMID:16914133"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal bipolar neuron differentiation","termid":"GO:0060040"}],"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":"rod bipolar cell differentiation","termid":"GO:1904389"}


id: GO:2000514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of CD4-positive, alpha-beta T cell activation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of alpha-beta T cell activation","termid":"GO:0046634"},{"relation_name":"regulates","term_name":"CD4-positive, alpha-beta T cell activation","termid":"GO:0035710"}],"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 CD4-positive, alpha-beta T cell activation","termid":"GO:2000514"}


id: PBO:0089745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Mpp10","termid":"PBO:0089745"}


id: MONDO:0018982
data:
  {"annotated_genes":["SJAG_01407"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011873"}]},"cv_name":"mondo","definition":"NPC is a complex lipid storage disease mainly characterized by the accumulation of unesterified cholesterol in the late endosomal/lysosomal compartment.","definition_xrefs":["PMID:21502308"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lysosomal storage disease","termid":"MONDO:0002561"},{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease (obsolete MONDO:0017037)","termid":"MONDO:0017037"},{"relation_name":"excluded_subClassOf","term_name":"obsolete sphingolipidosis with epilepsy (obsolete MONDO:0018299)","termid":"MONDO:0018299"},{"relation_name":"excluded_subClassOf","term_name":"obsolete neurometabolic disease (obsolete MONDO:0019058)","termid":"MONDO:0019058"},{"relation_name":"excluded_subClassOf","term_name":"lysosomal lipid storage disorder","termid":"MONDO:0019245"},{"relation_name":"excluded_subClassOf","term_name":"cerebral lipidosis with dementia","termid":"MONDO:0020143"},{"relation_name":"excluded_subClassOf","term_name":"obsolete unclassified primitive or secondary maculopathy (obsolete MONDO:0020244)","termid":"MONDO:0020244"},{"relation_name":"excluded_subClassOf","term_name":"supranuclear oculomotor palsy","termid":"MONDO:0020257"},{"relation_name":"is_a","term_name":"Niemann-Pick disease","termid":"MONDO:0001982"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01407":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005046","MONDO:0002525","MONDO:0002561","MONDO:0005066"],"is_obsolete":false,"name":"Niemann-Pick disease type C","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:67399","NORD:1509","ICD10CM:E75.242","SCTID:66751000","UMLS:C0220756","MESH:D052556","NANDO:1200063","Orphanet:646","icd11.foundation:812702125","GARD:7207"],"synonyms":[{"name":"NPC","type":"broad"},{"name":"Niemann Pick Disease Type C","type":"exact"}],"termid":"MONDO:0018982","terms_by_termid":{"MONDO:0011873":null},"xrefs":{"Monarch":{"xref_id":"0018982"}}}


id: PBO:0054974
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 2388","termid":"PBO:0054974"}


id: PBO:0087637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the eukaryotic translation initiation factor 3 (eIF3); component of unknown function; deletion causes defects in mitochondrial organization but not in growth or translation initiation; can rescue cytokinesis and mitochondrial organization defects of the Dictyostelium cluA- mutant; eIF3 is also involved in programmed stop codon readthrough","termid":"PBO:0087637"}


id: PBO:0002682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"box H/ACA snoRNP complex subunit Nhp2","termid":"PBO:0002682"}


id: MONDO:0007032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Prune belly syndrome is a rare congenital disorder, belonging to the group of fetal lower urinary tract obstructions (LUTO), involving variable dilation of the lower urinary tract in association with partial or complete absence of the lateral and inferior abdominal wall musculature and in males bilateral non-palpable undescended testes.","definition_xrefs":["Orphanet:2970"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"fetal lower urinary tract obstruction","termid":"MONDO:0018559"},{"relation_name":"is_a","term_name":"inherited kidney disorder","termid":"MONDO:0100191"}],"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":"prune belly syndrome","secondary_identifiers":["MedDRA:10051025","icd11.foundation:1393408621","GARD:7479","NCIT:C85033","NORD:1623","SCTID:5187006","DOID:0060889","UMLS:C0033770","MEDGEN:18718","OMIM:100100","NANDO:2200185","ICD9:756.71","MESH:D011535","MESH:C536477","ICD10CM:Q79.4"],"synonyms":[{"name":"Obrinsky syndrome","type":"exact"},{"name":"Obrisnksy syndrome","type":"exact"},{"name":"PBS","type":"related"},{"name":"abdominal muscle deficiency syndrome","type":"exact"},{"name":"abdominal muscles, absence of, with urinary tract Abnormality and cryptorchidism","type":"related"},{"name":"eagle-Barret syndrome","type":"exact"},{"name":"eagle-Barrett syndrome","type":"related"},{"name":"prune belly syndrome","type":"exact"},{"name":"syndrome of agenesis of abdominal muscles","type":"exact"},{"name":"triad syndrome","type":"exact"}],"termid":"MONDO:0007032","xrefs":{"Monarch":{"xref_id":"0007032"}}}


id: PBO:0005739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIN component scaffold protein, centriolin ortholog Cdc11","termid":"PBO:0005739"}


id: PBO:0110190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial membrane protein involved in heme biosynthesis, TMEM14 superfamily Aim19","termid":"PBO:0110190"}


id: PBO:0062499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily D member 4","termid":"PBO:0062499"}


id: GO:0021669
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to rhombomere 6. This process pertains to the initial formation of a structure from unspecified parts. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates. Rhombomeres are numbered in anterior to posterior order.","definition_xrefs":["GOC:curators","GOC:dgh","GOC:cls","GOC:dph","GOC:jid","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhombomere formation","termid":"GO:0021594"},{"relation_name":"part_of","term_name":"rhombomere 6 morphogenesis","termid":"GO:0021667"}],"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":"rhombomere 6 formation","termid":"GO:0021669"}


id: GO:0016027
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex of proteins that are involved in phototransduction and attached to the transient receptor potential (TRP) channel. The protein connections are mediated through inaD.","definition_xrefs":["PMID:9796815","GOC:hb","PMID:9010208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"},{"relation_name":"part_of","term_name":"rhabdomere","termid":"GO:0016028"},{"relation_name":"part_of","term_name":"extrinsic component of plasma membrane","termid":"GO:0019897"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"inaD signaling complex","synonyms":[{"name":"inaD signalling complex","type":"exact"}],"termid":"GO:0016027"}


id: PBO:0047427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fc epsilon receptor Ig","termid":"PBO:0047427"}


id: PATO:0001828
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A biological sex quality inhering in an individual or a population by virtue of having internal reproductive organs of male and external sexual characteristics of female.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudohermaphrodite","termid":"PATO:0001827"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"male pseudohermaphrodite","termid":"PATO:0001828"}


id: PBO:0034265
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_biological_homology_relationship_with","termid":"PBO:0034265"}


id: PBO:0063495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZ and LIM domain 3","termid":"PBO:0063495"}


id: FYPO:0000491
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 mitochondrial genome maintenance does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrial genome maintenance","termid":"FYPO:0000490"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished mitochondrial genome maintenance","synonyms":[{"name":"abolished mitochondrial genome maintenance during mitotic cell cycle","type":"related"},{"name":"absent mitochondrial genome maintenance","type":"exact"},{"name":"mitochondrial genome maintenance abolished","type":"exact"},{"name":"mitochondrial genome maintenance abolished during vegetative growth","type":"exact"},{"name":"mitochondrial genome maintenance: absent","type":"related"}],"termid":"FYPO:0000491"}


id: GO:0120112
data:
  {"annotated_genes":["SJAG_04162"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114209],"is_not":false,"summary":null,"term":"GO:0120112"}]},"cv_name":"biological_process","definition":"The directed movement of UDP-glucose from cytosol to endoplasmic reticulum.","definition_xrefs":["PMID:27587357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucose transmembrane transport","termid":"GO:0015786"},{"relation_name":"is_a","term_name":"cytosol to endoplasmic reticulum transport","termid":"GO:0046967"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04162":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"UDP-glucose transmembrane transport into endoplasmic reticulum","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0120112","terms_by_termid":{"GO:0120112":null}}


id: MONDO:0020022
data:
  {"annotated_genes":["SJAG_00112","SJAG_00639","SJAG_00991","SJAG_04084","SJAG_03120","SJAG_03067","SJAG_01818","SJAG_04123","SJAG_00754","SJAG_04824","SJAG_04067","SJAG_02723","SJAG_00653","SJAG_00900","SJAG_01260","SJAG_05346","SJAG_05277","SJAG_01970","SJAG_04907","SJAG_00379","SJAG_04822","SJAG_01712","SJAG_03328","SJAG_01645","SJAG_00773","SJAG_01791","SJAG_00289","SJAG_04321","SJAG_00637","SJAG_03601","SJAG_04902"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014601"},{"annotations":[87131],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014529"},{"annotations":[87001],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044701"},{"annotations":[87261],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013722"},{"annotations":[88355,88353,88352,88356,88354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011818"},{"annotations":[87160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014552"},{"annotations":[87747,87746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014716"},{"annotations":[88140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014349"},{"annotations":[88051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013853"},{"annotations":[88348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010190"},{"annotations":[88837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012890"},{"annotations":[88841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012891"},{"annotations":[88172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014370"},{"annotations":[87285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009166"},{"annotations":[87061],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012438"},{"annotations":[87050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012683"},{"annotations":[88800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013990"},{"annotations":[88142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014351"},{"annotations":[87997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032643"},{"annotations":[88700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032831"},{"annotations":[88251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030258"},{"annotations":[88252],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030259"},{"annotations":[87964,87965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030438"},{"annotations":[88656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014485"},{"annotations":[88135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054844"},{"annotations":[88253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030261"},{"annotations":[87833],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014874"},{"annotations":[88634],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010574"},{"annotations":[87363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014848"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"}],"gene_count":31,"genes_by_uniquename":{"SJAG_00112":null,"SJAG_00289":null,"SJAG_00379":null,"SJAG_00637":null,"SJAG_00639":null,"SJAG_00653":null,"SJAG_00754":null,"SJAG_00773":null,"SJAG_00900":null,"SJAG_00991":null,"SJAG_01260":null,"SJAG_01645":null,"SJAG_01712":null,"SJAG_01791":null,"SJAG_01818":null,"SJAG_01970":null,"SJAG_02723":null,"SJAG_03067":null,"SJAG_03120":null,"SJAG_03328":null,"SJAG_03601":null,"SJAG_04067":null,"SJAG_04084":null,"SJAG_04123":null,"SJAG_04321":null,"SJAG_04822":null,"SJAG_04824":null,"SJAG_04902":null,"SJAG_04907":null,"SJAG_05277":null,"SJAG_05346":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"is_obsolete":false,"name":"central nervous system malformation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2200118","Orphanet:98044","UMLS:C1839543","MESH:D009421","GARD:19394","ICD10CM:Q00-Q07","MEDGEN:374250"],"termid":"MONDO:0020022","terms_by_termid":{"MONDO:0009166":null,"MONDO:0010190":null,"MONDO:0010574":null,"MONDO:0011818":null,"MONDO:0012438":null,"MONDO:0012683":null,"MONDO:0012890":null,"MONDO:0012891":null,"MONDO:0013722":null,"MONDO:0013853":null,"MONDO:0013990":null,"MONDO:0014349":null,"MONDO:0014351":null,"MONDO:0014370":null,"MONDO:0014485":null,"MONDO:0014529":null,"MONDO:0014552":null,"MONDO:0014601":null,"MONDO:0014716":null,"MONDO:0014848":null,"MONDO:0014874":null,"MONDO:0030258":null,"MONDO:0030259":null,"MONDO:0030261":null,"MONDO:0030438":null,"MONDO:0032643":null,"MONDO:0032831":null,"MONDO:0044701":null,"MONDO:0054844":null},"xrefs":{"Monarch":{"xref_id":"0020022"}}}


id: GO:0002237
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 bacterial origin such as peptides derived from bacterial flagellin.","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 bacterium","termid":"GO:0009617"}],"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 bacterial origin","synonyms":[{"name":"response to bacteria associated molecule","type":"exact"},{"name":"response to bacterial associated molecule","type":"exact"},{"name":"response to bacterium associated molecule","type":"exact"}],"termid":"GO:0002237"}


id: GO:0102924
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2 H+ + gibberellin A44 + 2-oxoglutarate + O2 = gibberellin A98 + succinate + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A44,2-oxoglutarate:oxygen oxidoreductase activity (obsolete GO:0102924)","termid":"GO:0102924"}


id: GO:0003437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell communication that contributes to the shaping of the growth plate cartilage.","definition_xrefs":["GOC:dph","GOC:ascb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication","termid":"GO:0010646"},{"relation_name":"part_of","term_name":"growth plate cartilage morphogenesis","termid":"GO:0003422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell communication involved in growth plate cartilage morphogenesis","termid":"GO:0003437"}


id: GO:0140921
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of thermomorphogenesis.","definition_xrefs":["PMID:27250752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of post-embryonic development","termid":"GO:0048581"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of thermomorphogenesis","termid":"GO:0140920"},{"relation_name":"negatively_regulates","term_name":"thermomorphogenesis","termid":"GO:0140919"}],"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 thermomorphogenesis","termid":"GO:0140921"}


id: PBO:0070921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 29","termid":"PBO:0070921"}


id: MONDO:0020509
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Secondary syringomyelia is a rare medullar disease defined as a development of a fluid-filled cavity or syrinx within the spinal cord due to blockage of CSF circulation (e.g., due to basal archnoiditis, meningeal carcinomatosis, various mass lesions), spinal cord injury (e.g., due to trauma, radiation necrosis, hemorrhage, spinal abscess), spinal dysraphism or intramedullary tumors. It presents with neuropathic pain, numbness, muscular weakness, changes in tone or spasticity or autonomic changes (hyperhidrosis, heart rate or blood pressure instability). Selective loss of pain and temperature with relative preservation of dorsal column function (touch and pressure) are classic findings.","definition_xrefs":["Orphanet:99857"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syringomyelia","termid":"MONDO:0017987"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary syringomyelia","secondary_identifiers":["UMLS:C4749399","MEDGEN:1649806","GARD:19692"],"termid":"MONDO:0020509","xrefs":{"Monarch":{"xref_id":"0020509"}}}


id: MONDO:0030690
data:
  {"annotated_genes":["SJAG_03855"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88892],"is_not":false,"summary":null,"term":"MONDO:0030690"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary fibrosis and/or bone marrow failure, telomere-related","termid":"MONDO:0000148"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03855":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0019303"],"is_obsolete":false,"name":"pulmonary fibrosis and/or bone marrow failure, telomere-related, 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5676927","OMIM:619767","MEDGEN:1805650"],"synonyms":[{"name":"PFBMFT6","type":"exact"},{"name":"pulmonary fibrosis and/or bone marrow failure, telomere-related, 6","type":"exact"}],"termid":"MONDO:0030690","terms_by_termid":{"MONDO:0030690":null},"xrefs":{"Monarch":{"xref_id":"0030690"}}}


id: GO:0036283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the movement of a transcription factor from the cytoplasm to the nucleus under conditions of oxidative stress.","definition_xrefs":["PMID:9585505","GOC:al"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription factor import into nucleus in response to oxidative stress (obsolete GO:0036283)","synonyms":[{"name":"positive regulation of transcription factor import into nucleus in response to hydrogen peroxide","type":"related"}],"termid":"GO:0036283"}


id: MONDO:0017851
data:
  {"annotated_genes":["SJAG_02488"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033014"}]},"cv_name":"mondo","definition":"A rare genetic chronic skin disorder characterized by hyperkeratosis and transient erythema.","definition_xrefs":["NCIT:C84696"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Papillon-Lefevre disease","termid":"MONDO:0009490"},{"relation_name":"excluded_subClassOf","term_name":"obsolete erythrokeratoderma variabilis progressiva (obsolete MONDO:0017681)","termid":"MONDO:0017681"},{"relation_name":"is_a","term_name":"diffuse palmoplantar keratoderma","termid":"MONDO:0017666"},{"relation_name":"is_a","term_name":"erythrokeratoderma","termid":"MONDO:0019270"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02488":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"erythrokeratodermia variabilis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:317","DOID:0050467","MEDGEN:75587","icd11.foundation:551200965","UMLS:C0265961","MedDRA:10049048","GARD:16528","MESH:D056266","NORD:1285","OMIMPS:133200","MESH:C536154","Orphanet:316","SCTID:70041004","Orphanet:308166"],"synonyms":[{"name":"Darier-Gottron disease","type":"exact"},{"name":"EKV","type":"exact"},{"name":"EKVP","type":"related"},{"name":"Ichthyosis, Erythrokeratodermia Variabilis","type":"exact"},{"name":"erythrokeratodermia figurata variabilis","type":"exact"},{"name":"erythrokeratodermia figurata, congenital familial, in plaques","type":"related"},{"name":"erythrokeratodermia progressiva symmetrica","type":"exact"},{"name":"erythrokeratodermia variabilis","type":"exact"},{"name":"erythrokeratodermia variabilis ET progressiva","type":"related"},{"name":"erythrokeratodermia variabilis with erythema Gyratum Repens","type":"related"},{"name":"erythrokeratodermia variabilis with erythema gyratum repens","type":"related"},{"name":"erythrokeratodermia variabilis, Mendes da Costa type","type":"exact"},{"name":"erythrokeratodermia, progressive symmetric","type":"related"},{"name":"keratoderma palmoplantaris transgrediens","type":"related"},{"name":"keratosis extremitatum hereditaria progrediens","type":"related"},{"name":"keratosis palmoplantaris transgrediens et progrediens","type":"related"},{"name":"progressive symmetric erythrokeratodermia","type":"exact"},{"name":"progressive symmetric erythrokeratodermia, Gottron type","type":"exact"}],"termid":"MONDO:0017851","terms_by_termid":{"MONDO:0033014":null},"xrefs":{"Monarch":{"xref_id":"0017851"}}}


id: FYPO:0007192
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 rapid, back-and-forth movement of the mitotic spindle pole body (SPB), and associated chromosome movement, do not occur. Normally, SPB oscillation occurs during mitotic interphase (as well as prophase) but is restricted to a small space.","definition_xrefs":["PMID:31483748","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body-led chromosome movement during mitotic interphase","termid":"FYPO:0005348"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"abolished spindle pole body-led chromosome movement during mitotic interphase","synonyms":[{"name":"abolished mitotic SPB oscillation during mitotic interphase","type":"exact"},{"name":"abolished mitotic spindle pole body movement during mitotic interphase","type":"exact"},{"name":"abolished mitotic spindle pole body oscillation during mitotic interphase","type":"exact"},{"name":"abolished spindle pole body-led chromosome movement during interphase of mitotic cell cycle","type":"related"},{"name":"abolished spindle pole body-led chromosome movement during mitotic interphase during vegetative growth","type":"exact"},{"name":"mitotic spindle pole body oscillation abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0007192"}


id: PBO:0070710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 15","termid":"PBO:0070710"}


id: PBO:0062653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 13 subfamily C member 3","termid":"PBO:0062653"}


id: PBO:0081747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 677","termid":"PBO:0081747"}


id: PBO:0034321
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-transitively_provides_input_for","termid":"PBO:0034321"}


id: PBO:0052830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 223, pseudogene","termid":"PBO:0052830"}


id: GO:0046395
data:
  {"annotated_genes":["SJAG_03671","SJAG_03434","SJAG_02496","SJAG_01903","SJAG_00706","SJAG_03861","SJAG_03398","SJAG_03312","SJAG_03743","SJAG_04827","SJAG_02450","SJAG_03804","SJAG_04570","SJAG_00937","SJAG_04145","SJAG_02235","SJAG_00944","SJAG_00674","SJAG_02901","SJAG_02763","SJAG_00714","SJAG_04842","SJAG_00281","SJAG_01432","SJAG_03293","SJAG_00495","SJAG_02734","SJAG_03641"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009074"},{"annotations":[75562,72855,73178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000949"},{"annotations":[82067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019478"},{"annotations":[80645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036088"},{"annotations":[74919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001561"},{"annotations":[73059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009062"},{"annotations":[89201,90189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009450"},{"annotations":[79742,75859,98192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019464"},{"annotations":[102819,106895],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009436"},{"annotations":[70142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042853"},{"annotations":[80097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019544"},{"annotations":[80095,115041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010121"},{"annotations":[72558],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006533"},{"annotations":[115774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019450"},{"annotations":[93483,81317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006538"},{"annotations":[71936,79820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010133"},{"annotations":[73805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006567"},{"annotations":[74771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006574"},{"annotations":[82102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903457"},{"annotations":[115602],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042758"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of carboxylic acids, any organic acid containing one or more carboxyl (-COOH) groups.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic acid catabolic process","termid":"GO:0016054"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00281":null,"SJAG_00495":null,"SJAG_00674":null,"SJAG_00706":null,"SJAG_00714":null,"SJAG_00937":null,"SJAG_00944":null,"SJAG_01432":null,"SJAG_01903":null,"SJAG_02235":null,"SJAG_02450":null,"SJAG_02496":null,"SJAG_02734":null,"SJAG_02763":null,"SJAG_02901":null,"SJAG_03293":null,"SJAG_03312":null,"SJAG_03398":null,"SJAG_03434":null,"SJAG_03641":null,"SJAG_03671":null,"SJAG_03743":null,"SJAG_03804":null,"SJAG_03861":null,"SJAG_04145":null,"SJAG_04570":null,"SJAG_04827":null,"SJAG_04842":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"carboxylic acid catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"carboxylic acid breakdown","type":"exact"},{"name":"carboxylic acid catabolism","type":"exact"},{"name":"carboxylic acid degradation","type":"exact"}],"termid":"GO:0046395","terms_by_termid":{"GO:0000949":null,"GO:0001561":null,"GO:0006533":null,"GO:0006538":null,"GO:0006567":null,"GO:0006574":null,"GO:0009062":null,"GO:0009074":null,"GO:0009436":null,"GO:0009450":null,"GO:0010121":null,"GO:0010133":null,"GO:0019450":null,"GO:0019464":null,"GO:0019478":null,"GO:0019544":null,"GO:0036088":null,"GO:0042758":null,"GO:0042853":null,"GO:1903457":null}}


id: PBO:0057764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 2053","termid":"PBO:0057764"}


id: PBO:0057497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 615","termid":"PBO:0057497"}


id: PBO:0086940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ran GTPase; GTP binding protein (mammalian Ranp homolog) involved in the maintenance of nuclear organization, RNA processing and transport; regulated by Srm1p, Rna1p, Yrb1p, Yrb2p, Yrp4p, Yrb30p, Cse1p and Kap95p; GSP1 has a paralog, GSP2, that arose from the whole genome duplication","termid":"PBO:0086940"}


id: PBO:0001348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RecA family ATPase Rhp57","termid":"PBO:0001348"}


id: GO:0043711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a pilus, a short filamentous structure on a bacterial cell, flagella-like in structure and generally present in many copies.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell projection organization","termid":"GO:0030030"}],"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":"pilus organization","synonyms":[{"name":"pilus organisation","type":"exact"},{"name":"pilus organization and biogenesis","type":"related"}],"termid":"GO:0043711"}


id: FYPO:0004010
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 occurrence of translation of one or more ribosomal proteins is decreased.","definition_xrefs":["PMID:2839305","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased translation","termid":"FYPO:0001798"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0006551","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased translation of ribosomal proteins during vegetative growth","synonyms":[{"name":"decreased translation of ribosomal proteins during mitotic cell cycle","type":"related"},{"name":"reduced translation of ribosomal proteins during vegetative growth","type":"exact"}],"termid":"FYPO:0004010"}


id: PBO:0065837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB9A, member RAS oncogene family pseudogene 2","termid":"PBO:0065837"}


id: GO:1901840
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of RNA polymerase I regulatory region sequence-specific DNA binding.","definition_xrefs":["GOC:TermGenie","GOC:sart"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of RNA polymerase I regulatory region sequence-specific DNA binding (obsolete GO:1901840)","synonyms":[{"name":"down regulation of RNA polymerase I regulatory region sequence-specific DNA binding","type":"exact"},{"name":"down-regulation of RNA polymerase I regulatory region sequence-specific DNA binding","type":"exact"},{"name":"downregulation of RNA polymerase I regulatory region sequence-specific DNA binding","type":"exact"},{"name":"inhibition of RNA polymerase I regulatory region sequence-specific DNA binding","type":"narrow"}],"termid":"GO:1901840"}


id: GO:0060188
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein desumoylation. Protein desumoylation is the process in which a SUMO protein (small ubiquitin-related modifier) is cleaved from its target protein.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification by small protein conjugation or removal","termid":"GO:1903320"},{"relation_name":"regulates","term_name":"protein desumoylation","termid":"GO:0016926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0008150","GO:0070647"],"is_obsolete":false,"name":"regulation of protein desumoylation","termid":"GO:0060188"}


id: GO:0090062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of trehalose metabolism, the chemical reactions and pathways involving trehalose, a disaccharide that consists of two molecules of glucose and is isomeric with sucrose.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of carbohydrate metabolic process","termid":"GO:0006109"},{"relation_name":"regulates","term_name":"trehalose metabolic process","termid":"GO:0005991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of trehalose metabolic process","termid":"GO:0090062"}


id: PBO:0119984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGEF25 antisense RNA 1","termid":"PBO:0119984"}


id: PBO:0069484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 751, pseudogene","termid":"PBO:0069484"}


id: GO:0140702
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to cyclic GMP-AMP (cGAMP) nucleotide.","definition_xrefs":["PMID:23258412"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclic nucleotide binding","termid":"GO:0030551"}],"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":"cyclic GMP-AMP binding","termid":"GO:0140702"}


id: MONDO:0014598
data:
  {"annotated_genes":["SJAG_02384","SJAG_02848"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87002,87003],"is_not":false,"summary":null,"term":"MONDO:0014598"}]},"cv_name":"mondo","definition":"Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene.","definition_xrefs":["OMIM:616346","MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Lennox-Gastaut syndrome","termid":"MONDO:0016532"},{"relation_name":"is_a","term_name":"undetermined early-onset epileptic encephalopathy","termid":"MONDO:0018614"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"},{"relation_name":"is_a","term_name":"DNM1-encephalopathy and neurodevelopmental disorder","termid":"MONDO:0700339"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02384":null,"SJAG_02848":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 31A","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4225357","GARD:16094","DOID:0080437","MEDGEN:894942"],"synonyms":[{"name":"DEE31","type":"broad"},{"name":"DEE31A","type":"exact"},{"name":"DNM1 early infantile epileptic encephalopathy","type":"exact"},{"name":"DNM1-encephalopathy and neurodevelopmental disorder","type":"broad"},{"name":"DNM1-related epilepsy and neurodevelopmental disorder","type":"broad"},{"name":"EIEE31","type":"broad"},{"name":"developmental and epileptic encephalopathy 31","type":"broad"},{"name":"developmental and epileptic encephalopathy 31A, autosomal dominant","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in DNM1","type":"broad"},{"name":"epileptic encephalopathy, early infantile, 31","type":"broad"},{"name":"epileptic encephalopathy, early infantile, type 31","type":"broad"}],"termid":"MONDO:0014598","terms_by_termid":{"MONDO:0014598":null},"xrefs":{"Monarch":{"xref_id":"0014598"}}}


id: SO:0001628
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant located in the intergenic region, between genes.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feature_variant","termid":"SO:0001878"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intergenic_variant","secondary_identifiers":["http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences","http://snp.gs.washington.edu/SeattleSeqAnnotation137/HelpHowToUse.jsp","http://snpeff.sourceforge.net/SnpEff_manual.html"],"synonyms":[{"name":"ANNOVAR:intergenic","type":"related"},{"name":"Jannovar:intergenic_variant","type":"exact"},{"name":"Seattleseq:intergenic","type":"exact"},{"name":"VEP:intergenic_variant","type":"exact"},{"name":"intergenic","type":"exact"},{"name":"intergenic variant","type":"exact"},{"name":"snpEff:INTERGENIC","type":"exact"}],"termid":"SO:0001628"}


id: MONDO:0035819
data:
  {"annotated_genes":["SJAG_03892"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88314],"is_not":false,"summary":null,"term":"MONDO:0035819"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03892":null},"genotype_count":0,"is_obsolete":false,"name":"cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18020","MEDGEN:1780242","OMIM:619273","UMLS:C5543287","Orphanet:603448"],"synonyms":[{"name":"CIMDAG syndrome","type":"exact"}],"termid":"MONDO:0035819","terms_by_termid":{"MONDO:0035819":null},"xrefs":{"Monarch":{"xref_id":"0035819"}}}


id: RO:0002630
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Process(P1) directly negatively regulates process(P2) iff: P1 negatively regulates P2 via direct physical interaction between an agent executing P1 (or some part of P1) and an agent executing P2 (or some part of P2).  For example, if protein A has protein binding activity(P1) that targets protein B and this binding  negatively regulates the kinase activity (P2) of protein B then P1 directly negatively regulates P2.","direct_ancestors":[{"relation_name":"is_a","term_name":"negatively_regulates","termid":"RO:0002212"},{"relation_name":"is_a","term_name":"directly_regulates","termid":"RO:0002578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"directly_negatively_regulates","termid":"RO:0002630"}


id: PBO:0109370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 5","termid":"PBO:0109370"}


id: PBO:0042845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 53","termid":"PBO:0042845"}


id: PBO:0055115
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 2534","termid":"PBO:0055115"}


id: PBO:0071051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 53","termid":"PBO:0071051"}


id: PBO:0051577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 17 receptor A","termid":"PBO:0051577"}


id: GO:0016508
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: a medium-chain (3S)-3-hydroxyacyl-CoA = a medium-chain (2E)-enoyl-CoA + H2O. A long-chain acyl-CoA is an acyl-CoA thioester where the acyl chain contains 13 to 22 carbon atoms.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete long-chain-enoyl-CoA hydratase activity (obsolete GO:0016508)","termid":"GO:0016508"}


id: GO:0051009
data:
  {"annotated_genes":["SJAG_02972"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112336],"is_not":false,"summary":null,"term":"GO:0051009"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: O-acetyl-L-homoserine + hydrogen sulfide = homocysteine + acetate.","definition_xrefs":["RHEA:27822","MetaCyc:ACETYLHOMOSER-CYS-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetylhomoserine aminocarboxypropyltransferase activity","termid":"GO:0003961"},{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity","termid":"GO:0016835"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02972":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016829","GO:0016765","GO:0003824"],"is_obsolete":false,"name":"O-acetylhomoserine sulfhydrylase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"homocysteine synthase","type":"exact"}],"termid":"GO:0051009","terms_by_termid":{"GO:0051009":null}}


id: PBO:0091700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA ligase","termid":"PBO:0091700"}


id: PBO:0047779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FOXD1 antisense RNA 1","termid":"PBO:0047779"}


id: GO:0106395
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of a palmitic acid catabolic process.","definition_xrefs":["PMID:14677856"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of fatty acid metabolic process","termid":"GO:0045923"},{"relation_name":"is_a","term_name":"positive regulation of lipid catabolic process","termid":"GO:0050996"},{"relation_name":"is_a","term_name":"regulation of palmitic acid catabolic process","termid":"GO:0106393"},{"relation_name":"positively_regulates","term_name":"palmitic acid catabolic process","termid":"GO:1900534"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"positively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"positive regulation of palmitic acid catabolic process","termid":"GO:0106395"}


id: MONDO:0009077
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":"deafness, congenital, and familial myoclonic epilepsy","secondary_identifiers":["OMIM:220300","MEDGEN:346569","MESH:C565649","UMLS:C1857348"],"synonyms":[{"name":"deafness, congenital, and familial myoclonic epilepsy","type":"exact"}],"termid":"MONDO:0009077","xrefs":{"Monarch":{"xref_id":"0009077"}}}


id: PBO:0042949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 3","termid":"PBO:0042949"}


id: PBO:0062475
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 G member 3","termid":"PBO:0062475"}


id: GO:0048184
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to the peptide hormone follistatin.","definition_xrefs":["GOC:jid","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete follistatin binding (obsolete GO:0048184)","synonyms":[{"name":"follistatin binding","type":"exact"}],"termid":"GO:0048184"}


id: PBO:0050289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HNF1 homeobox B","termid":"PBO:0050289"}


id: PBO:0084965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetylglucosaminyltransferase; capable of modification of N-linked glycans in the Golgi apparatus","termid":"PBO:0084965"}


id: MONDO:0044217
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete asparagus, specific smell hypersensitivity (obsolete MONDO:0044217)","secondary_identifiers":["OMIM:108390"],"synonyms":[{"name":"asparagus, specific smell hypersensitivity","type":"related"}],"termid":"MONDO:0044217","xrefs":{"Monarch":{"xref_id":"0044217"}}}


id: PR:Q92355
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sen1 gene.","definition_xrefs":["UniProtKB:Q92355","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":"helicase sen1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6G9.10c","synonyms":[{"name":"Spom972h-sen1","type":"exact"}],"termid":"PR:Q92355"}


id: FYPO:0006851
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of one or more meiotic cell cycle phases is shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased duration of cell cycle phase","termid":"FYPO:0000410"},{"relation_name":"is_a","term_name":"abnormal meiotic cell cycle phase","termid":"FYPO:0002738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased duration of meiotic cell cycle phase","synonyms":[{"name":"reduced duration of meiotic cell cycle phase","type":"exact"}],"termid":"FYPO:0006851"}


id: GO:0120238
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The carbohydrate rich layer at the outermost periphery of a sperm cell.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycocalyx","termid":"GO:0030112"}],"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":"sperm glycocalyx","termid":"GO:0120238"}


id: PBO:0003111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation elongation factor EF-Ts Tsf1","termid":"PBO:0003111"}


id: PBO:0036079
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transport_along_microtubule_during_vegetative_growth","termid":"PBO:0036079"}


id: PBO:0086685
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; identified by SAGE","termid":"PBO:0086685"}


id: PBO:0001614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipase (predicted)","termid":"PBO:0001614"}


id: GO:0010469
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a signaling receptor activity. Receptor activity is when a molecule combines with an extracellular or intracellular messenger to initiate a change in cell activity.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"is_a","term_name":"regulation of molecular function","termid":"GO:0065009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of signaling receptor activity","synonyms":[{"name":"regulation of receptor activity","type":"broad"},{"name":"regulation of signalling receptor activity","type":"exact"}],"termid":"GO:0010469"}


id: PBO:0074897
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 71","termid":"PBO:0074897"}


id: PBO:0040451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase phospholipid transporting 11A","termid":"PBO:0040451"}


id: PBO:0060529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetyltransferase 2","termid":"PBO:0060529"}


id: MONDO:0016510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Epibulbar lipodermoid B preauricular appendages B polythelia is a branchial arch syndrome described in seven sibs of one Danish family and characterized by supernumerary nipples (polythelia), preauricular appendages and often binocular epibulbar lipodermoids or unilateral subconjunctival lipodermoids.","definition_xrefs":["Orphanet:231742"],"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":"epibulbar lipodermoid-preauricular appendage-polythelia syndrome","secondary_identifiers":["MEDGEN:1808551","UMLS:C5680927","GARD:20625"],"termid":"MONDO:0016510","xrefs":{"Monarch":{"xref_id":"0016510"}}}


id: FYPO:0001566
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 L-citrulline measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular amino acid level","termid":"FYPO:0003986"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular citrulline level","synonyms":[{"name":"increased cellular L-citrulline level","type":"exact"},{"name":"increased cellular citrulline level during mitotic cell cycle","type":"related"},{"name":"increased cellular citrulline level during vegetative growth","type":"exact"},{"name":"increased citrulline accumulation","type":"related"}],"termid":"FYPO:0001566"}


id: PBO:0004168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paxillin-like protein Pxl1","termid":"PBO:0004168"}


id: PBO:0057780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 2682","termid":"PBO:0057780"}


id: GO:0009525
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A flattened membranous vesicle containing cell wall components.","definition_xrefs":["ISBN:0943088399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"phragmosome","secondary_identifiers":["Wikipedia:Phragmosome"],"termid":"GO:0009525"}


id: MONDO:0800088
data:
  {"annotated_genes":["SJAG_04295","SJAG_02139","SJAG_05194","SJAG_01868","SJAG_05182","SJAG_04706","SJAG_05175","SJAG_04819"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87113,87114,87111,87115,87112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010027"},{"annotations":[87208,87209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009737"},{"annotations":[88585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015012"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":8,"genes_by_uniquename":{"SJAG_01868":null,"SJAG_02139":null,"SJAG_04295":null,"SJAG_04706":null,"SJAG_04819":null,"SJAG_05175":null,"SJAG_05182":null,"SJAG_05194":null},"genotype_count":0,"is_obsolete":false,"name":"lysosomal storage disease with skeletal involvement","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:93448","GARD:19203","ICD9:756.9","SCTID:279081001","SCTID:254069004"],"synonyms":[{"name":"dysostosis multiplex","type":"exact"}],"termid":"MONDO:0800088","terms_by_termid":{"MONDO:0009737":null,"MONDO:0010027":null,"MONDO:0015012":null},"xrefs":{"Monarch":{"xref_id":"0800088"}}}


id: PBO:0051241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (II)-53-1 (pseudogene)","termid":"PBO:0051241"}


id: GO:1990820
data:
  {"annotated_genes":["SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104189],"is_not":false,"summary":null,"term":"GO:1990820"}]},"cv_name":"biological_process","definition":"A process that occurs in response to signals generated as a result of mitotic DNA integrity checkpoint signaling.","definition_xrefs":["PMID:7548844"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to DNA integrity checkpoint signaling","termid":"GO:0072402"},{"relation_name":"is_a","term_name":"response to mitotic cell cycle checkpoint signaling","termid":"GO:0072414"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to mitotic DNA integrity checkpoint signaling","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"response to signal involved in mitotic DNA integrity checkpoint","type":"exact"}],"termid":"GO:1990820","terms_by_termid":{"GO:1990820":null}}


id: GO:0042999
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transport of Cystic Fibrosis Transmembrane conductance Regulator (CFTR) protein from the Golgi to the plasma membrane.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of Golgi to plasma membrane CFTR protein transport (obsolete GO:0042999)","termid":"GO:0042999"}


id: MONDO:1012556
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitral valve dysplasia, non-human animal","termid":"MONDO:1011652"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitral valve dysplasia, ass","secondary_identifiers":["OMIA:002521-9793"],"termid":"MONDO:1012556","xrefs":{"Monarch":{"xref_id":"1012556"}}}


id: GO:0018887
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 4-carboxy-4'-sulfoazobenzene, a sulfonated azo compound synthesized by nitro-amine condensation from sulfanilic acid and 4-nitrobenzoic acid.","definition_xrefs":["PMID:9603860"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"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"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0044281"],"is_obsolete":false,"name":"4-carboxy-4'-sulfoazobenzene metabolic process","secondary_identifiers":["UM-BBD_pathwayID:csab"],"synonyms":[{"name":"4-carboxy-4'-sulfoazobenzene metabolism","type":"exact"},{"name":"4-carboxy-4'-sulphoazobenzene metabolic process","type":"exact"},{"name":"4-carboxy-4'-sulphoazobenzene metabolism","type":"exact"}],"termid":"GO:0018887"}


id: PR:O14157
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- myp2 gene.","definition_xrefs":["UniProtKB:O14157","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":"myosin type-2 heavy chain 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4A8.05c","synonyms":[{"name":"Spom972h-myp2","type":"exact"},{"name":"myosin type II heavy chain 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14157"}


id: MONDO:0019162
data:
  {"annotated_genes":["SJAG_04335"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013782"}]},"cv_name":"mondo","definition":"A rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function.","definition_xrefs":["Orphanet:757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited pseudohypoaldosteronism","termid":"MONDO:0100323"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04335":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"pseudohypoaldosteronism type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1449844","NANDO:2200369","icd11.foundation:715347509","NCIT:C123252","GARD:4553","SCTID:15689008","ICD9:588.89","OMIMPS:145260","MEDGEN:259599"],"synonyms":[{"name":"Gordon hyperkalemia-hypertension syndrome","type":"exact"},{"name":"Gordon syndrome","type":"related"},{"name":"PHA2","type":"exact"},{"name":"PHAII","type":"exact"},{"name":"Spitzer-Weinstein syndrome","type":"exact"},{"name":"chloride shunt syndrome","type":"exact"},{"name":"familial hyperkalemic hypertension","type":"exact"},{"name":"hyperkalemia-hypertension syndrome, Gordon type","type":"exact"},{"name":"hyperpotassemia and hypertension familial","type":"related"},{"name":"hypertensive hyperkalemia","type":"exact"},{"name":"mineralocorticoid resistant hyperkalemia","type":"exact"},{"name":"pseudohypoaldosteronism, type 2","type":"exact"},{"name":"pseudohypoaldosteronism, type II","type":"exact"}],"termid":"MONDO:0019162","terms_by_termid":{"MONDO:0013782":null},"xrefs":{"Monarch":{"xref_id":"0019162"}}}


id: PBO:0078485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon AAT) 5-5","termid":"PBO:0078485"}


id: PBO:0082732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Rpd3L histone deacetylase complex; involved in transcriptional regulation of PHO5; affects termination of snoRNAs and cryptic unstable transcripts (CUTs); C-terminus shares significant sequence identity with the human candidate tumor suppressor p33-ING1 and its isoform ING3","termid":"PBO:0082732"}


id: PBO:0065650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase receptor type C associated protein","termid":"PBO:0065650"}


id: GO:0043491
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An intracellular signaling cassette that starts with phosphatidylinositol 3-kinase (PI3K) activation, production of phosphatidylinositol 3-phosphate (PI3P), activation of PDK1, which recruits and ending with the activation of protein kinase B (PKB, also known as Akt). PI3K is activated by cell surface receptors. Note that PTEN is an inhibitor of the pathway.","definition_xrefs":["PMID:22952397","PMID:20517722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signaling cassette","termid":"GO:0141124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"phosphatidylinositol 3-kinase/protein kinase B signal transduction","secondary_identifiers":["Reactome:R-HSA-198203","Reactome:R-HSA-198323","Reactome:R-HSA-198693"],"synonyms":[{"name":"AKT signal transduction","type":"related"},{"name":"AKT signaling","type":"related"},{"name":"AKT signaling cascade","type":"related"},{"name":"AKT signalling cascade","type":"related"},{"name":"PI3K-PKB/Akt pathway","type":"exact"},{"name":"PI3K/Akt signal transduction","type":"exact"},{"name":"PI3K/PKB signal transduction","type":"exact"},{"name":"PKB signal transduction","type":"related"},{"name":"PKB signaling","type":"related"},{"name":"PKB signaling cascade","type":"related"},{"name":"PKB signalling cascade","type":"related"},{"name":"phosphatidylinositol 3-kinase signaling/protein kinase B signal transduction","type":"exact"},{"name":"protein kinase B signal transduction","type":"related"},{"name":"protein kinase B signaling","type":"related"},{"name":"protein kinase B signaling cascade","type":"related"},{"name":"protein kinase B signalling cascade","type":"related"}],"termid":"GO:0043491"}


id: PR:Q9URW1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAPJ695.01c gene.","definition_xrefs":["UniProtKB:Q9URW1","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":"UPF0321 protein PJ695.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPJ695.01c","synonyms":[{"name":"Spom972h-SPAPJ695.01c","type":"exact"}],"termid":"PR:Q9URW1"}


id: PBO:0116247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-type ATPase V0 subunit f","termid":"PBO:0116247"}


id: PBO:0053739
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 964","termid":"PBO:0053739"}


id: GO:0034676
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An integrin complex that comprises one alpha6 subunit and one beta4 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":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"integrin alpha6-beta4 complex","synonyms":[{"name":"ITGA6-ITGB4 complex","type":"narrow"},{"name":"alpha6-beta4 integrin complex","type":"exact"}],"termid":"GO:0034676"}


id: PBO:0044989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAH-box helicase 40 pseudogene 1","termid":"PBO:0044989"}


id: PBO:0090262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L4","termid":"PBO:0090262"}


id: PBO:0058534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6079","termid":"PBO:0058534"}


id: MONDO:0003542
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dental pulp disorder","termid":"MONDO:0003394"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dental pulp calcification","secondary_identifiers":["UMLS:C0011401","ICD10CM:K04.2","DOID:5608","MEDGEN:41471","icd11.foundation:1672640309","MESH:D003784","SCTID:57602001"],"synonyms":[{"name":"pulp calcification","type":"exact"},{"name":"pulp calcifications","type":"exact"},{"name":"pulpal calcifications","type":"exact"}],"termid":"MONDO:0003542","xrefs":{"Monarch":{"xref_id":"0003542"}}}


id: GO:0015161
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transbilayer of capsular-polysaccharides (Und-PP-GlcNAc-ManNAcA-Fuc4NAc (lipid III)) from the inner to the outer leaflet of the cytoplasmic membrane during the assembly of ECA. Capsular polysaccharides make up the capsule, a protective structure surrounding some species of bacteria and fungi.","definition_xrefs":["GOC:ai","GOC:mtg_transport","PMID:16816184","PMID:12621029"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floppase activity","termid":"GO:0140328"}],"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:0140303"}],"interesting_parent_ids":["GO:0005215","GO:0140303","GO:0003674"],"is_obsolete":false,"name":"lipid III floppase activity","secondary_identifiers":["TC:2.A.66.2.12","TC:2.A.66.2.3"],"synonyms":[{"name":"capsular polysaccharide transmembrane transporter activity","type":"related"},{"name":"capsule polysaccharide transporter activity","type":"broad"},{"name":"undecaprenol-pyrophosphate O-antigen flippase activity","type":"exact"}],"termid":"GO:0015161"}


id: PBO:0070656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 27","termid":"PBO:0070656"}


id: PR:Q8WZK5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC839.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q8WZK5"],"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":"arrestin-related trafficking adapter C839.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC839.02","synonyms":[{"name":"Spom972h-SPBC839.02","type":"exact"}],"termid":"PR:Q8WZK5"}


id: PBO:0083744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential component of the outer kinetochore MIND complex; joins kinetochore subunits contacting DNA to those contacting microtubules; required for kinetochore bi-orientation and accurate chromosome segregation; complex consists of Mtw1p, Nnf1p, Nsl1p and Dsn1p; homologous to metazoan CENP-H proteins","termid":"PBO:0083744"}


id: PBO:0091676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1773 family protein","termid":"PBO:0091676"}


id: MONDO:1010115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"C8 deficiency that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"c8 deficiency, non-human animal","secondary_identifiers":["OMIA:000156"],"termid":"MONDO:1010115","xrefs":{"Monarch":{"xref_id":"1010115"}}}


id: PBO:0003149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-AN1 type zinc finger protein","termid":"PBO:0003149"}


id: PBO:0078075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocation associated membrane protein 1 like 1","termid":"PBO:0078075"}


id: PR:O94334
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pof13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94334"],"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":"F-box protein pof13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1271.01c","synonyms":[{"name":"Spom972h-pof13","type":"exact"}],"termid":"PR:O94334"}


id: MONDO:0800045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoinflammatory syndrome, familial, Behcet-like","termid":"MONDO:0031384"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoinflammatory syndrome, familial, Behcet-like 1","secondary_identifiers":["DOID:0080944","UMLS:C4225218","MEDGEN:898541","Orphanet:674762","GARD:17848","Orphanet:476102","OMIM:616744"],"synonyms":[{"name":"AISBL","type":"broad"},{"name":"Behçet-like disease due to HA20","type":"exact"},{"name":"Behçet-like disease due to haploinsufficiency of A20","type":"exact"},{"name":"autoinflammatory syndrome, familial, Behcet-like","type":"broad"},{"name":"autoinflammatory syndrome, familial, Behcet-like 1","type":"exact"},{"name":"hereditary paediatric Behçet-like disease","type":"exact"},{"name":"hereditary pediatric Behçet-like disease","type":"exact"}],"termid":"MONDO:0800045","xrefs":{"Monarch":{"xref_id":"0800045"}}}


id: GO:0005990
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of lactose, the disaccharide galactopyranosyl-glucose.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lactose metabolic process","termid":"GO:0005988"},{"relation_name":"is_a","term_name":"disaccharide catabolic process","termid":"GO:0046352"}],"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:0008150","GO:0005975"],"is_obsolete":false,"name":"lactose catabolic process","synonyms":[{"name":"lactose breakdown","type":"exact"},{"name":"lactose catabolism","type":"exact"},{"name":"lactose degradation","type":"exact"}],"termid":"GO:0005990"}


id: GO:0046412
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving phenylmercury acetate, an organomercurial compound composed of a mercury atom attached to a benzene ring and an acetate group.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organometal metabolic process","termid":"GO:0018942"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"}],"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":"phenylmercury acetate metabolic process","synonyms":[{"name":"phenylmercury acetate metabolism","type":"exact"}],"termid":"GO:0046412"}


id: PR:O94322
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC725.03 gene.","definition_xrefs":["UniProtKB:O94322","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C725.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC725.03","synonyms":[{"name":"Spom972h-SPBC725.03","type":"exact"}],"termid":"PR:O94322"}


id: PR:Q9P7G8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A UPF0382 inner membrane protein YgdD that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01977","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":"UPF0382 membrane protein C1782.12c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1782.12c","secondary_identifiers":["UniProtKB:Q9P7G8"],"synonyms":[{"name":"Spom972h-ygdD","type":"exact"}],"termid":"PR:Q9P7G8"}


id: PBO:0081555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 474","termid":"PBO:0081555"}


id: PBO:0042881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 221","termid":"PBO:0042881"}


id: PBO:0070032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1329, pseudogene","termid":"PBO:0070032"}


id: PBO:0057224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 380","termid":"PBO:0057224"}


id: GO:0038026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of reelin (a secreted glycoprotein) to a receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:bf","PMID:12827279","PMID:20223215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway","termid":"GO:0007166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"reelin-mediated signaling pathway","synonyms":[{"name":"reeler-mediated signaling pathway","type":"exact"},{"name":"reelin-mediated signal transduction pathway","type":"exact"},{"name":"reelin-mediated signalling pathway","type":"exact"}],"termid":"GO:0038026"}


id: GO:0035670
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an ovary that produces an ovule over time, from its formation to the mature structure. The ovary is the enlarged basal portion of a carpel and matures into a fruit. An ovule is the multicellular structure that gives rise to and contains the female reproductive cells, and develops into a seed.","definition_xrefs":["GOC:tb","ISBN:0879015322","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"},{"relation_name":"part_of","term_name":"carpel development","termid":"GO:0048440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"plant-type ovary development","termid":"GO:0035670"}


id: PR:Q09897
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cfh1 gene.","definition_xrefs":["UniProtKB:Q09897","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":"chitin synthase regulatory factor 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24B11.10c","synonyms":[{"name":"Chs four homolog 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-cfh1","type":"exact"}],"termid":"PR:Q09897"}


id: GO:0071561
data:
  {"annotated_genes":["SJAG_01329","SJAG_01116","SJAG_04552","SJAG_04221"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[78971,108135,108836,117041],"is_not":false,"summary":null,"term":"GO:0071561"}]},"cv_name":"cellular_component","definition":"An organelle membrane contact site formed between the vacuole membrane and the outer nuclear membrane. In S. cerevisiae these contacts are mediated through direct physical interaction between Vac8p and Nvj1p.","definition_xrefs":["PMID:16709156","GOC:jp","PMID:16806880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle membrane contact site","termid":"GO:0044232"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01116":null,"SJAG_01329":null,"SJAG_04221":null,"SJAG_04552":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"nucleus-vacuole junction","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"NV junction","type":"exact"},{"name":"NVJ","type":"exact"},{"name":"nucleus-vacuole membrane contact site","type":"exact"}],"termid":"GO:0071561","terms_by_termid":{"GO:0071561":null}}


id: FYPO:0002727
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of saccharopine dehydrogenase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal saccharopine dehydrogenase activity","termid":"FYPO:0002726"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000661","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"decreased saccharopine dehydrogenase activity","synonyms":[{"name":"reduced saccharopine dehydrogenase activity","type":"exact"}],"termid":"FYPO:0002727"}


id: PBO:0047658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 9 pseudogene 1","termid":"PBO:0047658"}


id: MONDO:0858992
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive spastic paraplegia type 87 (obsolete MONDO:0858992)","termid":"MONDO:0858992","xrefs":{"Monarch":{"xref_id":"0858992"}}}


id: PBO:0051492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin superfamily member 9B","termid":"PBO:0051492"}


id: PBO:0053274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukocyte immunoglobulin like receptor B1","termid":"PBO:0053274"}


id: GO:0002300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a CD8-positive, alpha-beta intraepithelial T cell. Intraepithelial T cells are found among epithelial cells in mucosal areas and have distinct phenotypes and developmental pathways.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-beta intraepithelial T cell differentiation","termid":"GO:0002299"},{"relation_name":"is_a","term_name":"CD8-positive, alpha-beta T cell differentiation","termid":"GO:0043374"}],"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":"CD8-positive, alpha-beta intraepithelial T cell differentiation","synonyms":[{"name":"CD8-positive, alpha-beta intraepithelial T cell development","type":"related"},{"name":"CD8-positive, alpha-beta intraepithelial T lymphocyte differentiation","type":"exact"},{"name":"CD8-positive, alpha-beta intraepithelial T-cell differentiation","type":"exact"},{"name":"CD8-positive, alpha-beta intraepithelial T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002300"}


id: PBO:0057368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548aj-2","termid":"PBO:0057368"}


id: SO:0002114
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A protein coding transcript that contains a CDS but has one or more splice junctions >50bp downstream of stop codon, making it susceptible to nonsense mediated decay.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein_coding_primary_transcript","termid":"SO:0000120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMD_transcript","secondary_identifiers":["http://www.gencodegenes.org/gencode_biotypes.html"],"synonyms":[{"name":"NMD transcript","type":"exact"},{"name":"nonsense mediated decay transcript","type":"exact"},{"name":"protein_coding_NMD","type":"exact"}],"termid":"SO:0002114"}


id: PBO:0042596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CMT1A duplicated region transcript 11","termid":"PBO:0042596"}


id: MOD:01601
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-121 reagent derivatized residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"iTRAQ8plex-121 reporter+balance reagent acylated residue","termid":"MOD:01577"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter fragment","termid":"MOD:01593"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-121 reporter fragment","synonyms":[{"name":"4-methyl-1-methylidenepiperazin-1-ium","type":"exact"}],"termid":"MOD:01601"}


id: RO:0002638
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A sub-relation of endoparasite-of in which the parasite inhabits the spaces between host cells.","direct_ancestors":[{"relation_name":"is_a","term_name":"endoparasite_of","termid":"RO:0002634"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intercellular_endoparasite_of","termid":"RO:0002638"}


id: PBO:0091736
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heteromeric(8)","termid":"PBO:0091736"}


id: PBO:0089287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane transporter","termid":"PBO:0089287"}


id: GO:0099166
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic specialization membrane of a symmetric synapse 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:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of postsynaptic specialization membrane of symmetric synapse (obsolete GO:0099166)","synonyms":[{"name":"intrinsic to postsynaptic specialization membrane of symmetric synapse","type":"narrow"}],"termid":"GO:0099166"}


id: GO:0042696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The beginning of the menstrual cycle; the first menstrual cycle in an individual.","definition_xrefs":["GOC:curators","PMID:16311040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"menstrual cycle phase","termid":"GO:0022601"}],"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":"menarche","secondary_identifiers":["Wikipedia:Menarche"],"termid":"GO:0042696"}


id: GO:0001228
data:
  {"annotated_genes":["SJAG_01243","SJAG_05006","SJAG_00802","SJAG_02472","SJAG_02730","SJAG_02810","SJAG_02326","SJAG_03519","SJAG_01916","SJAG_04855","SJAG_03241","SJAG_04749","SJAG_01583","SJAG_01532","SJAG_05247","SJAG_03183","SJAG_00698","SJAG_00693","SJAG_00210","SJAG_04813","SJAG_00266","SJAG_02218","SJAG_04009","SJAG_03143","SJAG_00163","SJAG_04839","SJAG_04036","SJAG_03538","SJAG_00987","SJAG_01694","SJAG_01307","SJAG_02252","SJAG_05288","SJAG_04092","SJAG_01062","SJAG_02406","SJAG_03879","SJAG_02311","SJAG_03484","SJAG_04249","SJAG_05153","SJAG_04388","SJAG_04712","SJAG_03346","SJAG_03735"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57351,61932,62171,64076,64963,68165,68560,70263,74169,76507,76725,77493,79091,79133,81116,81832,89364,89728,89798,90225,90561,90812,91239,93691,94528,98359,99074,100201,101287,102290,104075,106242,107647,107922,109391,109794,110628,110867,111179,111516,113714,115525,116421,117914,118313],"is_not":false,"summary":null,"term":"GO:0001228"}]},"cv_name":"molecular_function","definition":"A DNA-binding transcription factor activity that activates or increases transcription of specific gene sets transcribed by RNA polymerase II.","definition_xrefs":["GOC:aruk","GOC:txnOH-2018","PMID:27145859","PMID:20737563"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-binding transcription factor activity, RNA polymerase II-specific","termid":"GO:0000981"},{"relation_name":"is_a","term_name":"DNA-binding transcription activator activity","termid":"GO:0001216"}],"gene_count":45,"genes_by_uniquename":{"SJAG_00163":null,"SJAG_00210":null,"SJAG_00266":null,"SJAG_00693":null,"SJAG_00698":null,"SJAG_00802":null,"SJAG_00987":null,"SJAG_01062":null,"SJAG_01243":null,"SJAG_01307":null,"SJAG_01532":null,"SJAG_01583":null,"SJAG_01694":null,"SJAG_01916":null,"SJAG_02218":null,"SJAG_02252":null,"SJAG_02311":null,"SJAG_02326":null,"SJAG_02406":null,"SJAG_02472":null,"SJAG_02730":null,"SJAG_02810":null,"SJAG_03143":null,"SJAG_03183":null,"SJAG_03241":null,"SJAG_03346":null,"SJAG_03484":null,"SJAG_03519":null,"SJAG_03538":null,"SJAG_03735":null,"SJAG_03879":null,"SJAG_04009":null,"SJAG_04036":null,"SJAG_04092":null,"SJAG_04249":null,"SJAG_04388":null,"SJAG_04712":null,"SJAG_04749":null,"SJAG_04813":null,"SJAG_04839":null,"SJAG_04855":null,"SJAG_05006":null,"SJAG_05153":null,"SJAG_05247":null,"SJAG_05288":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140110"},{"rel_name":"is_a","termid":"GO:0003700"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0001216"}],"interesting_parent_ids":["GO:0140110","GO:0003700","GO:0003674","GO:0001216"],"is_obsolete":false,"name":"DNA-binding transcription activator activity, RNA polymerase II-specific","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-9856549","GO:0001213","GO:0001209","Reactome:R-HSA-9856604","Reactome:R-HSA-9856550","GO:0001205","GO:0001077","Reactome:R-HSA-9856539","Reactome:R-HSA-9856548","GO:0001212","GO:0001211","Reactome:R-HSA-9856546"],"synonyms":[{"name":"RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription","type":"narrow"},{"name":"RNA polymerase II distal enhancer sequence-specific DNA-binding transcription factor activity involved in positive regulation of transcription","type":"narrow"},{"name":"RNA polymerase II transcription regulatory region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription","type":"exact"},{"name":"RNA polymerase II transcriptional activator activity, copper ion regulated proximal promoter sequence-specific DNA binding","type":"narrow"},{"name":"RNA polymerase II transcriptional activator activity, metal ion regulated core promoter proximal region sequence-specific binding","type":"narrow"},{"name":"RNA polymerase II transcriptional activator activity, metal ion regulated proximal promoter sequence-specific DNA binding","type":"narrow"},{"name":"RNA polymerase II transcriptional activator activity, zinc ion regulated core promoter proximal region sequence-specific binding","type":"narrow"},{"name":"RNA polymerase II transcriptional activator activity, zinc ion regulated proximal promoter sequence-specific DNA binding","type":"narrow"},{"name":"copper ion regulated core promoter proximal region sequence-specific DNA binding RNA polymerase II transcription factor activity involved in positive regulation of transcription","type":"narrow"},{"name":"distal enhancer DNA-binding transcription activator activity, RNA polymerase II-specific","type":"narrow"},{"name":"metal ion regulated core promoter proximal region sequence-specific DNA binding RNA polymerase II transcription factor activity involved in positive regulation of transcription","type":"narrow"},{"name":"metal ion regulated sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription","type":"narrow"},{"name":"proximal promoter DNA-binding transcription activator activity, RNA polymerase II-specific","type":"narrow"},{"name":"sequence-specific distal enhancer binding RNA polymerase II transcription factor activity involved in positive regulation of transcription","type":"narrow"},{"name":"transcriptional activator activity, RNA polymerase II core promoter proximal region sequence-specific binding","type":"narrow"},{"name":"transcriptional activator activity, RNA polymerase II distal enhancer sequence-specific DNA binding","type":"narrow"},{"name":"transcriptional activator activity, RNA polymerase II proximal promoter sequence-specific DNA binding","type":"narrow"},{"name":"transcriptional activator activity, RNA polymerase II transcription regulatory region sequence-specific DNA binding","type":"exact"},{"name":"transcriptional activator activity, metal ion regulated sequence-specific DNA binding","type":"narrow"},{"name":"zinc ion regulated core promoter proximal region sequence-specific DNA binding RNA polymerase II transcription factor activity involved in positive regulation of transcription","type":"narrow"}],"termid":"GO:0001228","terms_by_termid":{"GO:0001228":null}}


id: MONDO:0022462
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by bilateral anophthalmia, esophageal atresia, and cryptorchidism. This is an n-of-1 use case where only one patient or family has been described with this disorder.","definition_xrefs":["PMID:1352427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anophthalmia esophageal atresia cryptorchidism","termid":"MONDO:0022462","xrefs":{"Monarch":{"xref_id":"0022462"}}}


id: MONDO:0005132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A herpesvirus infection caused by Cytomegalovirus. Healthy individuals generally do not produce symptoms. However, the infection may be life-threatening in affected immunocompromised patients. The virus may cause retinitis, esophagitis, gastritis, and colitis. Morphologically, it is characterized by the presence of intranuclear inclusion bodies.","definition_xrefs":["NCIT:C53649"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytomegalovirus infection","secondary_identifiers":["MEDGEN:8239","UMLS:C0010823","MESH:D003586","SCTID:28944009","EFO:0001062","ICD9:078.5"],"synonyms":[{"name":"CMV infection","type":"exact"},{"name":"Cytomegaloviral infection","type":"exact"},{"name":"HCMV infection","type":"exact"}],"termid":"MONDO:0005132","xrefs":{"Monarch":{"xref_id":"0005132"}}}


id: FYPO:0007442
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 endoplasmic reticulum membrane is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0006378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to endoplasmic reticulum membrane","synonyms":[{"name":"normal protein localization to ER membrane","type":"exact"},{"name":"normal protein localization to endoplasmic reticulum membrane during mitotic cell cycle","type":"related"},{"name":"normal protein localization to endoplasmic reticulum membrane during vegetative growth","type":"exact"}],"termid":"FYPO:0007442"}


id: PBO:0072574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonucleotide reductase M2 polypeptide pseudogene 2","termid":"PBO:0072574"}


id: PBO:0056242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mago homolog 3, pseudogene","termid":"PBO:0056242"}


id: MONDO:0001562
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hiatus hernia","termid":"MONDO:0007721"}],"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":"displacement of cardia through esophageal hiatus","secondary_identifiers":["MEDGEN:510622","UMLS:C0158674","DOID:12641","ICD10CM:Q40.1","ICD9:750.6","SCTID:47028006"],"synonyms":[{"name":"congenital hiatus hernia","type":"exact"}],"termid":"MONDO:0001562","xrefs":{"Monarch":{"xref_id":"0001562"}}}


id: PR:P87244
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- alp16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87244"],"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":"spindle pole body component alp16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4G3.19","synonyms":[{"name":"Spom972h-alp16","type":"exact"},{"name":"altered polarity protein 16 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87244"}


id: PR:000059591
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An arresting-related substrate adaptor Any1 (Schizosaccharomyces pombe) that has been ubiquitinated at the position equivalent to Lys-263 of the amino acid sequence represented by UniProtKB:O60150. Example: UniProtKB:O60150, Lys-263, MOD:01148.","definition_xrefs":["PRO:DAN","PomBase:VW","PMID:24876389"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Any1/Ub(K263)","pombase_gene_id":"SPBC18H10.20c","synonyms":[{"name":"Any1/Ub(K263)","type":"exact"},{"name":"PomBase_original_PRO_term_name: arrestin-related substrate adaptor Any1 ubiquitinated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-any1/Ubiq:1","type":"exact"},{"name":"UniProtKB:O60150, Lys-263, MOD:01148","type":"exact"}],"termid":"PR:000059591"}


id: MONDO:1010297
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteoarthritis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory disease, non-human animal","termid":"MONDO:1011327"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoarthritis, non-human animal","secondary_identifiers":["OMIA:000747"],"termid":"MONDO:1010297","xrefs":{"Monarch":{"xref_id":"1010297"}}}


id: GO:0007354
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification of the anterior/posterior axis of the embryo by products of genes expressed in the zygote; exemplified in insects by the gap genes, pair rule genes and segment polarity gene cascade.","definition_xrefs":["ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior/posterior axis specification, embryo","termid":"GO:0008595"}],"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":"zygotic determination of anterior/posterior axis, embryo","termid":"GO:0007354"}


id: PBO:0063711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PGM5 antisense RNA 1","termid":"PBO:0063711"}


id: MONDO:0001285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"endometriosis","termid":"MONDO:0005133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endometriosis of pelvic peritoneum","secondary_identifiers":["UMLS:C0156345","ICD10CM:N80.3","DOID:11429","ICD9:617.3","MEDGEN:510249","icd11.foundation:1015401835","SCTID:198251001"],"termid":"MONDO:0001285","xrefs":{"Monarch":{"xref_id":"0001285"}}}


id: GO:0141125
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: queuosine34 in tRNA + UDP-alpha-D-galactose = H+ + O-5''-beta-D-galactosylqueuosine34 in tRNATyr + UDP. Substrates include tRNA(Tyr) and tRNA(Asp).","definition_xrefs":["PMID:37992713"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0140098","GO:0140101","GO:0003674","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"tRNA-queuosine(34) galactosyltransferase activity","secondary_identifiers":["RHEA:78231"],"synonyms":[{"name":"tRNA queuosine galactosyltransferase activity","type":"broad"},{"name":"tRNA queuosine(34) galactosyltransferase activity","type":"exact"}],"termid":"GO:0141125"}


id: PBO:0033755
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_spindle_pole_body_organization","termid":"PBO:0033755"}


id: GO:0099168
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic specialization membrane of a symmetric synapse consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete extrinsic component of postsynaptic specialization membrane of symmetric synapse (obsolete GO:0099168)","termid":"GO:0099168"}


id: PBO:0005473
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nbs1-Interacting Protein 1","termid":"PBO:0005473"}


id: PBO:0045553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 5 pseudogene 2","termid":"PBO:0045553"}


id: FYECO:0000260
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells were blocked using hydroxyurea and subsequently released from the block.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping condition combinations","termid":"FYECO:0000238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HU block and release","termid":"FYECO:0000260"}


id: MONDO:0700210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Enterovirus infectious disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enterovirus infectious disease, non-human animal","termid":"MONDO:0700210","xrefs":{"Monarch":{"xref_id":"0700210"}}}


id: GO:0002377
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of immunoglobulin due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"production of molecular mediator of immune response","termid":"GO:0002440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"immunoglobulin production","secondary_identifiers":["GO:0048305","GO:0002378"],"synonyms":[{"name":"antibody production","type":"exact"},{"name":"immunoglobulin biosynthetic process","type":"narrow"},{"name":"immunoglobulin secretion","type":"narrow"}],"termid":"GO:0002377"}


id: GO:0047747
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: (1) ATP + cholate + CoA = AMP + diphosphate + choloyl-CoA and (2) ATP + (25R)-3alpha,7alpha,12alpha-trihydroxy-5beta-cholestan-26-oate + CoA = AMP + diphosphate + (25R)-3alpha,7alpha,12alpha-trihydroxy-5beta-cholestanoyl-CoA. This reaction is the first step in the conjugation of bile acids with amino acids, converting bile acids into their acyl-CoA thioesters. Chenodeoxycholate, deoxycholate, lithocholate and trihydroxycoprostanoate can also act as substrates.","definition_xrefs":["EC:6.2.1.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-ligase activity","termid":"GO:0016405"},{"relation_name":"is_a","term_name":"acid-thiol ligase activity","termid":"GO:0016878"}],"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:0016874"}],"interesting_parent_ids":["GO:0003674","GO:0016874","GO:0003824"],"is_obsolete":false,"name":"cholate-CoA ligase activity","secondary_identifiers":["GO:0047477","MetaCyc:CHOLATE--COA-LIGASE-RXN"],"synonyms":[{"name":"3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanate--CoA ligase activity","type":"related"},{"name":"3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanate-CoA ligase activity","type":"exact"},{"name":"3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanate:CoA ligase (AMP-forming) activity","type":"related"},{"name":"3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoate-CoA ligase activity","type":"related"},{"name":"3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoate-CoA synthetase activity","type":"related"},{"name":"3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl coenzyme A synthetase activity","type":"related"},{"name":"3alpha,7alpha,12alpha-trihydroxy-5beta-cholestanate-CoA ligase activity","type":"related"},{"name":"3alpha,7alpha,12alpha-trihydroxy-5beta-cholestanate:CoA ligase (AMP-forming)","type":"related"},{"name":"3alpha,7alpha,12alpha-trihydroxy-5beta-cholestanoate-CoA ligase activity","type":"related"},{"name":"3alpha,7alpha,12alpha-trihydroxy-5beta-cholestanoate-CoA synthetase activity","type":"related"},{"name":"3alpha,7alpha,12alpha-trihydroxy-5beta-cholestanoyl coenzyme A synthetase activity","type":"related"},{"name":"BAL activity","type":"related"},{"name":"THCA-CoA ligase activity","type":"related"},{"name":"bile acid CoA ligase activity","type":"related"},{"name":"bile acid coenzyme A ligase activity","type":"related"},{"name":"cholate thiokinase activity","type":"related"},{"name":"cholate:CoA ligase (AMP-forming)","type":"related"},{"name":"cholic acid:CoA ligase activity","type":"related"},{"name":"cholic thiokinase activity","type":"related"},{"name":"choloyl coenzyme A synthetase activity","type":"related"},{"name":"choloyl-CoA synthetase activity","type":"related"},{"name":"cholyl-CoA synthetase activity","type":"related"},{"name":"trihydroxycoprostanoyl-CoA synthetase activity","type":"related"}],"termid":"GO:0047747"}


id: GO:1900923
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glycine import into a cell.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amino acid import across plasma membrane","termid":"GO:0010958"},{"relation_name":"is_a","term_name":"regulation of organic acid transport","termid":"GO:0032890"},{"relation_name":"regulates","term_name":"glycine import across plasma membrane","termid":"GO:1903804"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"regulation of glycine import across plasma membrane","synonyms":[{"name":"regulation of glycine import","type":"broad"}],"termid":"GO:1900923"}


id: MONDO:1012253
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spastic paresis, non-human animal","termid":"MONDO:1011859"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spastic paresis, cattle","secondary_identifiers":["OMIA:000928-9913"],"termid":"MONDO:1012253","xrefs":{"Monarch":{"xref_id":"1012253"}}}


id: MONDO:0001395
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"keratitis","termid":"MONDO:0003085"}],"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":"macular keratitis","secondary_identifiers":["DOID:11871","ICD9:370.22","MEDGEN:509772","SCTID:2853006","icd11.foundation:1283506871","UMLS:C0155076","ICD10CM:H16.11"],"termid":"MONDO:0001395","xrefs":{"Monarch":{"xref_id":"0001395"}}}


id: PBO:0054080
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 1430","termid":"PBO:0054080"}


id: PBO:0041617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium binding protein 2","termid":"PBO:0041617"}


id: MONDO:0019095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Plague is a severe bacterial infection caused by the gram-negative bacterium Yersinia pestis.","definition_xrefs":["Orphanet:707"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"Yersinia infectious disease","termid":"MONDO:0007023"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plague","secondary_identifiers":["ICD9:020.9","EFO:0009425","MedDRA:10061416","ICD9:020","MedDRA:10035148","NCIT:C85015","icd11.foundation:1596449540","MESH:D015009","ICD9:136.8","SCTID:58750007","MEDGEN:10785","GARD:18702","MESH:D010930","UMLS:C0032064","DOID:3482","ICD10CM:A20","NORD:1583"],"synonyms":[{"name":"Yersiniosis","type":"broad"},{"name":"black death","type":"related"},{"name":"infection by Yersinia pestis","type":"related"},{"name":"pest","type":"related"},{"name":"pestilential fever","type":"related"},{"name":"plague","type":"exact"}],"termid":"MONDO:0019095","xrefs":{"Monarch":{"xref_id":"0019095"}}}


id: MONDO:1012064
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Ancon dwarfism, non-human animal","termid":"MONDO:1011941"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ancon dwarfism, sheep","secondary_identifiers":["OMIA:000302-9940"],"termid":"MONDO:1012064","xrefs":{"Monarch":{"xref_id":"1012064"}}}


id: PBO:0109135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SHOX homeobox","termid":"PBO:0109135"}


id: MONDO:0014812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration (obsolete MONDO:0014812)","termid":"MONDO:0014812","xrefs":{"Monarch":{"xref_id":"0014812"}}}


id: PBO:0046481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERCC excision repair 6, chromatin remodeling factor","termid":"PBO:0046481"}


id: PBO:0059538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded transcription factor binding site X","termid":"PBO:0059538"}


id: GO:0006651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of diacylglycerol, a glyceride in which any two of the R groups (positions not specified) are acyl groups while the remaining R group can be either H or an alkyl group.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diacylglycerol metabolic process","termid":"GO:0046339"},{"relation_name":"is_a","term_name":"acylglycerol biosynthetic process","termid":"GO:0046463"}],"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":"diacylglycerol biosynthetic process","synonyms":[{"name":"diacylglycerol anabolism","type":"exact"},{"name":"diacylglycerol biosynthesis","type":"exact"},{"name":"diacylglycerol formation","type":"exact"},{"name":"diacylglycerol synthesis","type":"exact"},{"name":"diglyceride biosynthesis","type":"exact"}],"termid":"GO:0006651"}


id: GO:0009264
data:
  {"annotated_genes":["SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035863"},{"annotations":[81188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046081"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a deoxyribonucleotide, a compound consisting of deoxyribonucleoside (a base linked to a deoxyribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide catabolic process","termid":"GO:0009166"},{"relation_name":"is_a","term_name":"deoxyribonucleotide metabolic process","termid":"GO:0009262"},{"relation_name":"is_a","term_name":"carbohydrate derivative catabolic process","termid":"GO:1901136"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04487":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"deoxyribonucleotide catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"deoxyribonucleotide breakdown","type":"exact"},{"name":"deoxyribonucleotide catabolism","type":"exact"},{"name":"deoxyribonucleotide degradation","type":"exact"}],"termid":"GO:0009264","terms_by_termid":{"GO:0035863":null,"GO:0046081":null}}


id: PBO:0043031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHMP4A pseudogene 1","termid":"PBO:0043031"}


id: GO:0016114
data:
  {"annotated_genes":["SJAG_03715","SJAG_03352","SJAG_04568","SJAG_00413","SJAG_00580","SJAG_00624","SJAG_04499","SJAG_04307","SJAG_01474","SJAG_03349","SJAG_04865","SJAG_03360"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116745,115587,75987,96220,90466,81815,101380,103675,108339,111305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010142"},{"annotations":[101381,111306],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033386"},{"annotations":[67746,62511],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016104"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of terpenoids, any member of a class of compounds characterized by an isoprenoid chemical structure.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpenoid metabolic process","termid":"GO:0006721"},{"relation_name":"is_a","term_name":"isoprenoid biosynthetic process","termid":"GO:0008299"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00413":null,"SJAG_00580":null,"SJAG_00624":null,"SJAG_01474":null,"SJAG_03349":null,"SJAG_03352":null,"SJAG_03360":null,"SJAG_03715":null,"SJAG_04307":null,"SJAG_04499":null,"SJAG_04568":null,"SJAG_04865":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"terpenoid biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Terpenoid"],"synonyms":[{"name":"terpenoid anabolism","type":"exact"},{"name":"terpenoid biosynthesis","type":"exact"},{"name":"terpenoid formation","type":"exact"},{"name":"terpenoid synthesis","type":"exact"}],"termid":"GO:0016114","terms_by_termid":{"GO:0010142":null,"GO:0016104":null,"GO:0033386":null}}


id: PBO:0088932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycosylceramide biosynthesis protein Cwh43","termid":"PBO:0088932"}


id: GO:0102149
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-[(2E,6E)-farnesyl]-L-cysteine + O2 + H2O = (2-trans,6-trans)-farnesal + L-cysteine + hydrogen peroxide.","definition_xrefs":["EC:1.8.3.6","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor","termid":"GO:0016670"}],"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":"farnesylcysteine lyase activity","secondary_identifiers":["RHEA:30231","MetaCyc:RXN-11623"],"termid":"GO:0102149"}


id: GO:0001619
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Combining with lysosphingolipid or lysophosphatidic acid to initiate a change in cell activity.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete lysosphingolipid and lysophosphatidic acid receptor activity (obsolete GO:0001619)","synonyms":[{"name":"lysosphingolipid and lysophosphatidic acid receptor activity","type":"exact"}],"termid":"GO:0001619"}


id: MONDO:0971032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acquired metabolic disease that is characterized by ethanol fermentation in the bladder and the absence of alcoholic intoxication.","definition_xrefs":["DOID:0081456"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired metabolic disease","termid":"MONDO:0006504"}],"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":"bladder fermentation syndrome","termid":"MONDO:0971032","xrefs":{"Monarch":{"xref_id":"0971032"}}}


id: PATO:0000396
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An intensity which is extremely bad or unpleasant in type or degree or effect or force.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intensity","termid":"PATO:0000049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"severe intensity","termid":"PATO:0000396"}


id: PBO:0050400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein C pseudogene 1","termid":"PBO:0050400"}


id: GO:2000721
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of transcription from RNA polymerase II promoter that is involved in smooth muscle cell differentiation.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter involved in smooth muscle cell differentiation (obsolete GO:2000721)","synonyms":[{"name":"activation of global transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"related"},{"name":"activation of global transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"related"},{"name":"activation of transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"exact"},{"name":"activation of transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"exact"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"related"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter of nonstriated muscle cell differentiation","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter of smooth muscle cell differentiation","type":"related"},{"name":"positive regulation of transcription from Pol II promoter of nonstriated muscle cell differentiation","type":"exact"},{"name":"positive regulation of transcription from Pol II promoter of smooth muscle cell differentiation","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter, global of nonstriated muscle cell differentiation","type":"related"},{"name":"positive regulation of transcription from RNA polymerase II promoter, global of smooth muscle cell differentiation","type":"related"},{"name":"stimulation of global transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"related"},{"name":"stimulation of global transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"related"},{"name":"stimulation of transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"exact"},{"name":"stimulation of transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"exact"},{"name":"up regulation of global transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"related"},{"name":"up regulation of global transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"related"},{"name":"up regulation of transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"exact"},{"name":"up regulation of transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"exact"},{"name":"up-regulation of global transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"related"},{"name":"up-regulation of global transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"related"},{"name":"up-regulation of transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"exact"},{"name":"up-regulation of transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"exact"},{"name":"upregulation of global transcription from RNA polymerase II promoter of nonstriated muscle cell differentiation","type":"related"},{"name":"upregulation of global transcription from RNA polymerase II promoter of smooth muscle cell differentiation","type":"exact"}],"termid":"GO:2000721"}


id: FYPO:0006610
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 a protein that is normally localized intermittently to the Cdr2 medial cortical node complex is associated with the complex for periods of longer duration than normal.","definition_xrefs":["PomBase:mah","PMID:29514920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal intermittent protein localization to Cdr2 medial cortical node complex","termid":"FYPO:0006607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"increased protein dwell time during intermittent localization to Cdr2 medial cortical node complex","synonyms":[{"name":"increased duration of bursts of intermittent protein localization to Cdr2 medial cortical node complex","type":"related"},{"name":"increased duration of protein localization bursts to Cdr2 medial cortical node complex","type":"related"},{"name":"increased duration of protein visits to Cdr2 medial cortical node complex","type":"related"},{"name":"increased protein dwell time during intermittent localization to Cdr2 medial cortical node complex during mitotic cell cycle","type":"related"},{"name":"increased protein dwell time during intermittent localization to Cdr2 medial cortical node complex during vegetative growth","type":"exact"},{"name":"increased protein dwell time during transient localization to Cdr2 medial cortical node complex","type":"exact"}],"termid":"FYPO:0006610"}


id: PR:Q9P7N0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- meu32 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7N0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 11 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.08c","synonyms":[{"name":"Spom972h-meu32","type":"exact"},{"name":"meiotic expression up-regulated protein 32 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7N0"}


id: PR:Q9P6I6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1198.03c gene.","definition_xrefs":["UniProtKB:Q9P6I6","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1198.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.03c","synonyms":[{"name":"Spom972h-SPBC1198.03c","type":"exact"}],"termid":"PR:Q9P6I6"}


id: PBO:0044999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DIAPH3 antisense RNA 2","termid":"PBO:0044999"}


id: PBO:0049797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperpolarization activated cyclic nucleotide gated potassium channel 3","termid":"PBO:0049797"}


id: GO:0022409
data:
  {"annotated_genes":["SJAG_03484","SJAG_01253","SJAG_02380","SJAG_00910","SJAG_03802","SJAG_04191"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107703,113206,110576,117983,115923,110450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900735"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the rate or extent of cell adhesion to another cell.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell-cell adhesion","termid":"GO:0022407"},{"relation_name":"is_a","term_name":"positive regulation of cell adhesion","termid":"GO:0045785"},{"relation_name":"positively_regulates","term_name":"cell-cell adhesion","termid":"GO:0098609"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00910":null,"SJAG_01253":null,"SJAG_02380":null,"SJAG_03484":null,"SJAG_03802":null,"SJAG_04191":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"positive regulation of cell-cell adhesion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of cell-cell adhesion","type":"narrow"},{"name":"stimulation of cell-cell adhesion","type":"narrow"},{"name":"up regulation of cell-cell adhesion","type":"exact"},{"name":"up-regulation of cell-cell adhesion","type":"exact"},{"name":"upregulation of cell-cell adhesion","type":"exact"}],"termid":"GO:0022409","terms_by_termid":{"GO:1900735":null}}


id: GO:0045875
data:
  {"annotated_genes":["SJAG_05978","SJAG_03591","SJAG_01716","SJAG_00369","SJAG_00823","SJAG_01825"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93517,108068,108166,108391,109220,117177],"is_not":false,"summary":null,"term":"GO:0045875"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of sister chromatid cohesion.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sister chromatid cohesion","termid":"GO:0007063"},{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"negative regulation of chromosome organization","termid":"GO:2001251"},{"relation_name":"negatively_regulates","term_name":"sister chromatid cohesion","termid":"GO:0007062"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00369":null,"SJAG_00823":null,"SJAG_01716":null,"SJAG_01825":null,"SJAG_03591":null,"SJAG_05978":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of sister chromatid cohesion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of sister chromatid cohesion","type":"exact"},{"name":"down-regulation of sister chromatid cohesion","type":"exact"},{"name":"downregulation of sister chromatid cohesion","type":"exact"},{"name":"inhibition of sister chromatid cohesion","type":"narrow"}],"termid":"GO:0045875","terms_by_termid":{"GO:0045875":null}}


id: _global:complete_evidence_for_feature
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"B is complete_evidence_for_feature A if the extent (5' and 3' boundaries) and internal boundaries of B fully support the extent and internal boundaries of A.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"evidence_for_feature","termid":"_global:evidence_for_feature"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complete_evidence_for_feature","termid":"_global:complete_evidence_for_feature"}


id: PBO:0069129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 379, pseudogene","termid":"PBO:0069129"}


id: GO:0051599
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 hydrostatic pressure stimulus. Hydrostatic pressure is the force acting on an object in a system where the fluid is at rest (as opposed to moving). The weight of the fluid above the object creates pressure on it.","definition_xrefs":["Wikipedia:Hydrostatic_pressure"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"response to water","termid":"GO:0009415"}],"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 hydrostatic pressure","synonyms":[{"name":"response to biomechanical stress","type":"broad"},{"name":"response to static fluid pressure","type":"exact"}],"termid":"GO:0051599"}


id: SO:0001092
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A binding site that, in the polypeptide molecule, interacts selectively and non-covalently with metal ions.","definition_xrefs":["SO:cb","UniProt:curation_manual","EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metal_binding_site","termid":"SO:0001656"},{"relation_name":"is_a","term_name":"molecular_contact_region","termid":"SO:0100002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"polypeptide_metal_contact","secondary_identifiers":["BS:00027"],"synonyms":[{"name":"metal_binding","type":"related"}],"termid":"SO:0001092"}


id: MONDO:0007295
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A childhood-onset epilepsy syndrome that is characterized by onset of seizures between 3 and 14 years (peak 8-9 years) that usually resolve by age 13 years, but can occasionally occur up to age 18 years of age. Both sexes are affected. Antecedent, birth and neonatal history is normal. A history of febrile seizure (in 5-15%) may be seen. A history of Panayiotopoulos syndrome may be present in a very small number of cases. Neurological exam and head size is normal. Development and cognition prior to onset of seizures is normal. During the course of the active epilepsy, behavioral and neuropsychological deficits may be found, particularly in language and executive functioning. These deficits improve when seizures remit.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"epilepsy","termid":"MONDO:0005027"},{"relation_name":"excluded_subClassOf","term_name":"Landau-Kleffner syndrome","termid":"MONDO:0009509"},{"relation_name":"is_a","term_name":"familial partial epilepsy","termid":"MONDO:0017704"},{"relation_name":"is_a","term_name":"childhood-onset self-limited focal epilepsy syndrome","termid":"MONDO:0800502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"self-limited epilepsy with centrotemporal spikes","secondary_identifiers":["GARD:10287","NCIT:C116538","UMLS:C0376532","MEDGEN:138210","DOID:3329","SCTID:44145005","Orphanet:1945","icd11.foundation:1046279423","OMIM:117100","ICD9:345.80"],"synonyms":[{"name":"BCECTS","type":"exact"},{"name":"BECRS","type":"exact"},{"name":"BECTS","type":"exact"},{"name":"BRE","type":"exact"},{"name":"Rolandic epilepsy","type":"exact"},{"name":"benign Rolandic epilepsy","type":"exact"},{"name":"benign Rolandic epilepsy (BRE)","type":"exact"},{"name":"benign Rolandic epilepsy of childhood (BREC)","type":"exact"},{"name":"benign childhood epilepsy with centrotemporal spike","type":"exact"},{"name":"benign childhood epilepsy with centrotemporal spikes","type":"exact"},{"name":"benign epilepsy of childhood with centrotemporal spikes","type":"exact"},{"name":"benign epilepsy of childhood with centrotemporal spikes (BECCT)","type":"related"},{"name":"benign epilepsy with centro-temporal spikes (BECTS)","type":"related"},{"name":"benign epilepsy with centrotemporal spikes","type":"exact"},{"name":"benign familial epilepsy of childhood with rolandic spikes","type":"exact"},{"name":"centralopathic epilepsy","type":"exact"},{"name":"centrotemporal epilepsy","type":"exact"},{"name":"centrotemporal epilepsy, isolated cases","type":"exact"},{"name":"childhood epilepsy with centrotemporal spikes","type":"exact"},{"name":"sylvan seizures","type":"exact"},{"name":"temporal-central focal epilepsy","type":"exact"}],"termid":"MONDO:0007295","xrefs":{"Monarch":{"xref_id":"0007295"}}}


id: PBO:0086826
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; YNL165W is not an essential gene","termid":"PBO:0086826"}


id: MONDO:0008048
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy.","definition_xrefs":["Orphanet:169189"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"congenital structural myopathy","termid":"MONDO:0002921"},{"relation_name":"is_a","term_name":"centronuclear myopathy","termid":"MONDO:0018947"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant centronuclear myopathy","secondary_identifiers":["GARD:12719","DOID:0111217","MEDGEN:1645741","NCIT:C126689","DOID:0111223","OMIM:614408","UMLS:C4551952","OMIM:160150","SCTID:716696006"],"synonyms":[{"name":"AD-CNM","type":"exact"},{"name":"CNM1","type":"exact"},{"name":"CNM3","type":"related"},{"name":"DNM2-related centronuclear myopathy","type":"related"},{"name":"autosomal dominant centronuclear myopathy","type":"exact"},{"name":"autosomal dominant centronuclear myopathy caused by mutation in MYF6","type":"exact"},{"name":"centronuclear myopathy 1","type":"exact"},{"name":"centronuclear myopathy, autosomal dominant","type":"exact"},{"name":"centronuclear myopathy, autosomal, modifier of","type":"exact"},{"name":"myopathy, centronuclear, 1","type":"exact"},{"name":"myopathy, centronuclear, 3","type":"exact"},{"name":"myopathy, centronuclear, autosomal dominant","type":"exact"},{"name":"myopathy, centronuclear, type 1","type":"exact"},{"name":"myopathy, centronuclear, type 3","type":"exact"},{"name":"myotubular myopathy, autosomal dominant","type":"exact"}],"termid":"MONDO:0008048","xrefs":{"Monarch":{"xref_id":"0008048"}}}


id: GO:0004697
data:
  {"annotated_genes":["SJAG_01787","SJAG_00610"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[69334],"is_not":false,"summary":null,"term":"GO:0004697"},{"annotations":[92542],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004699"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + a protein = ADP + a phosphoprotein. This reaction requires diacylglycerol.","definition_xrefs":["EC:2.7.11.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004672"}],"interesting_parent_ids":["GO:0016740","GO:0004672","GO:0016301","GO:0003674","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"diacylglycerol-dependent serine/threonine kinase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-450550","Reactome:R-HSA-751040","Reactome:R-HSA-5623667","Reactome:R-HSA-374664","Reactome:R-HSA-909552","Reactome:R-HSA-8932284","Reactome:R-HSA-9626817","Reactome:R-HSA-9796053","Reactome:R-HSA-927889","Reactome:R-HSA-5218805","Reactome:R-HSA-5671749","Reactome:R-HSA-450533","Reactome:R-HSA-429698","Reactome:R-HSA-1433508","Reactome:R-HSA-9632858","GO:0004701","Reactome:R-HSA-2730863","Reactome:R-HSA-5218823","Reactome:R-HSA-198314","Reactome:R-HSA-8934446","Reactome:R-HSA-5138432","Reactome:R-HSA-2179413","Reactome:R-HSA-9010681","Reactome:R-HSA-5229194","Reactome:R-HSA-193703","Reactome:R-HSA-5625784","Reactome:R-HSA-9021357","Reactome:R-HSA-74615"],"synonyms":[{"name":"ATP:protein phosphotransferase (diacylglycerol-dependent) activity","type":"related"},{"name":"PKC","type":"related"},{"name":"PKC activity","type":"exact"},{"name":"PKCalpha","type":"related"},{"name":"PKCbeta","type":"related"},{"name":"PKCdelta","type":"related"},{"name":"PKCepsilon","type":"related"},{"name":"PKCgamma","type":"related"},{"name":"Pkc1p","type":"related"},{"name":"STK24","type":"related"},{"name":"cPKC","type":"related"},{"name":"cPKCalpha","type":"related"},{"name":"cPKCbeta","type":"related"},{"name":"cPKCgamma","type":"related"},{"name":"diacylglycerol-activated phospholipid-dependent PKC activity","type":"exact"},{"name":"diacylglycerol-activated phospholipid-dependent protein kinase C activity","type":"exact"},{"name":"nPKC","type":"related"},{"name":"nPKCdelta","type":"related"},{"name":"nPKCepsilon","type":"related"},{"name":"nPKCeta","type":"related"},{"name":"nPKCtheta","type":"related"},{"name":"protein kinase Cepsilon activity","type":"narrow"}],"termid":"GO:0004697","terms_by_termid":{"GO:0004697":null,"GO:0004699":null}}


id: PBO:0110023
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Social Distancing Gene","termid":"PBO:0110023"}


id: MONDO:0015489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete predominantly medium-vessel vasculitis (obsolete MONDO:0015489)","secondary_identifiers":["Orphanet:156143"],"termid":"MONDO:0015489","xrefs":{"Monarch":{"xref_id":"0015489"}}}


id: MONDO:0000601
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A hypersensitivity reaction type II disease that involves the genitourinary system.","definition_xrefs":["MONDO:patterns/location"],"gene_count":0,"genotype_count":0,"name":"obsolete autoimmune disorder of urogenital tract (obsolete MONDO:0000601)","secondary_identifiers":["DOID:0060049"],"synonyms":[{"name":"autoimmune disease of genitourinary system","type":"exact"},{"name":"genitourinary system autoimmune disease","type":"exact"},{"name":"genitourinary system hypersensitivity reaction type II disease","type":"exact"}],"termid":"MONDO:0000601","xrefs":{"Monarch":{"xref_id":"0000601"}}}


id: PBO:0079031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon AAC) 1-4","termid":"PBO:0079031"}


id: GO:1905421
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of plant organ morphogenesis.","definition_xrefs":["GO_REF:0000058","GOC:tb","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"regulates","term_name":"plant organ morphogenesis","termid":"GO:1905392"}],"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 plant organ morphogenesis","termid":"GO:1905421"}


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


id: MONDO:0002545
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disease involving the spinal cord.","direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system disorder","termid":"MONDO:0002602"}],"gene_count":40,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00106":null,"SJAG_00668":null,"SJAG_00754":null,"SJAG_00853":null,"SJAG_01260":null,"SJAG_01317":null,"SJAG_01352":null,"SJAG_01466":null,"SJAG_01522":null,"SJAG_01537":null,"SJAG_02242":null,"SJAG_02286":null,"SJAG_02289":null,"SJAG_02399":null,"SJAG_02509":null,"SJAG_02695":null,"SJAG_02919":null,"SJAG_03170":null,"SJAG_03328":null,"SJAG_03345":null,"SJAG_03495":null,"SJAG_03598":null,"SJAG_03712":null,"SJAG_03815":null,"SJAG_03894":null,"SJAG_03923":null,"SJAG_04042":null,"SJAG_04084":null,"SJAG_04156":null,"SJAG_04178":null,"SJAG_04321":null,"SJAG_04387":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04489":null,"SJAG_04567":null,"SJAG_04907":null,"SJAG_05289":null,"SJAG_07000":null},"genotype_count":0,"is_obsolete":false,"name":"spinal cord disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D013118","SCTID:48522003","ICD9:336.9","UMLS:C0037928","DOID:319","ICD9:336.8","MEDGEN:11550","EFO:0009488","NCIT:C97110"],"synonyms":[{"name":"disease of spinal cord","type":"exact"},{"name":"disease of the spinal cord","type":"exact"},{"name":"disease or disorder of spinal cord","type":"exact"},{"name":"disorder of spinal cord","type":"exact"},{"name":"myelopathy","type":"related"},{"name":"spinal cord disease","type":"exact"},{"name":"spinal cord disease or disorder","type":"exact"},{"name":"spinal cord disorder","type":"exact"}],"termid":"MONDO:0002545","terms_by_termid":{"MONDO:0007103":null,"MONDO:0008025":null,"MONDO:0008026":null,"MONDO:0008453":null,"MONDO:0008458":null,"MONDO:0009669":null,"MONDO:0009672":null,"MONDO:0009673":null,"MONDO:0010043":null,"MONDO:0010056":null,"MONDO:0010190":null,"MONDO:0010338":null,"MONDO:0010459":null,"MONDO:0010532":null,"MONDO:0010936":null,"MONDO:0011120":null,"MONDO:0011223":null,"MONDO:0011436":null,"MONDO:0011585":null,"MONDO:0011879":null,"MONDO:0012077":null,"MONDO:0012080":null,"MONDO:0012890":null,"MONDO:0012891":null,"MONDO:0012945":null,"MONDO:0013243":null,"MONDO:0013501":null,"MONDO:0013715":null,"MONDO:0013853":null,"MONDO:0013884":null,"MONDO:0014485":null,"MONDO:0014531":null,"MONDO:0014874":null,"MONDO:0015353":null,"MONDO:0030860":null,"MONDO:0060585":null,"MONDO:0859529":null},"xrefs":{"Monarch":{"xref_id":"0002545"}}}


id: PBO:0038722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin gamma 1 pseudogene 17","termid":"PBO:0038722"}


id: PBO:0044567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deleted in azoospermia like","termid":"PBO:0044567"}


id: PR:A6X980
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sfc7 gene.","definition_xrefs":["UniProtKB:A6X980","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 tau subunit sfc7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1250.07","synonyms":[{"name":"Spom972h-sfc7","type":"exact"},{"name":"TFIIIC subunit sfc7 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"transcription factor C subunit 7 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:A6X980"}


id: PBO:0114080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific methyltransferase","termid":"PBO:0114080"}


id: PBO:0002985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homologous Pmf1 factor 1, implicated in isoleucine biosynthesis (predicted)","termid":"PBO:0002985"}


id: PBO:0038366
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_component_process","termid":"PBO:0038366"}


id: PR:O42944
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- omh2 gene.","definition_xrefs":["UniProtKB:O42944","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":"O-glycoside alpha-1,2-mannosyltransferase homolog 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16H5.09c","synonyms":[{"name":"Spom972h-omh2","type":"exact"}],"termid":"PR:O42944"}


id: GO:0110079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of placenta blood vessel development.","definition_xrefs":["GOC:rph","GOC:BHF_miRNA","PMID:27748453","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vasculature development","termid":"GO:1901342"},{"relation_name":"regulates","term_name":"placenta blood vessel development","termid":"GO:0060674"}],"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 placenta blood vessel development","termid":"GO:0110079"}


id: PBO:0075586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine peptidase inhibitor Kazal type 13","termid":"PBO:0075586"}


id: GO:0046120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of any one of a family of organic molecules consisting of a purine or pyrimidine base covalently bonded to a sugar deoxyribose (a deoxyribonucleoside).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyribonucleoside metabolic process","termid":"GO:0009120"},{"relation_name":"is_a","term_name":"nucleoside biosynthetic process","termid":"GO:0009163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"deoxyribonucleoside biosynthetic process","synonyms":[{"name":"deoxyribonucleoside anabolism","type":"exact"},{"name":"deoxyribonucleoside biosynthesis","type":"exact"},{"name":"deoxyribonucleoside formation","type":"exact"},{"name":"deoxyribonucleoside synthesis","type":"exact"}],"termid":"GO:0046120"}


id: PBO:0041882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cation channel sperm associated 1","termid":"PBO:0041882"}


id: GO:0030289
data:
  {"annotated_genes":["SJAG_00823","SJAG_00369"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[74310,109218],"is_not":false,"summary":null,"term":"GO:0030289"}]},"cv_name":"cellular_component","definition":"A protein serine/threonine phosphatase complex formed by the catalytic subunit of protein phosphatase 4 plus one or more regulatory subunits.","definition_xrefs":["GOC:bhm","PMID:10026142"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine phosphatase complex","termid":"GO:0008287"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00369":null,"SJAG_00823":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":"protein phosphatase 4 complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0030289","terms_by_termid":{"GO:0030289":null}}


