# terms

id: GO:1901435
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of toluene catabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"regulation of toluene catabolic process","termid":"GO:1901434"},{"relation_name":"is_a","term_name":"negative regulation of toluene metabolic process","termid":"GO:1901438"},{"relation_name":"negatively_regulates","term_name":"toluene catabolic process","termid":"GO:0042203"}],"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 toluene catabolic process","synonyms":[{"name":"down regulation of toluene breakdown","type":"exact"},{"name":"down regulation of toluene catabolic process","type":"exact"},{"name":"down regulation of toluene catabolism","type":"exact"},{"name":"down regulation of toluene degradation","type":"exact"},{"name":"down-regulation of toluene breakdown","type":"exact"},{"name":"down-regulation of toluene catabolic process","type":"exact"},{"name":"down-regulation of toluene catabolism","type":"exact"},{"name":"down-regulation of toluene degradation","type":"exact"},{"name":"downregulation of toluene breakdown","type":"exact"},{"name":"downregulation of toluene catabolic process","type":"exact"},{"name":"downregulation of toluene catabolism","type":"exact"},{"name":"downregulation of toluene degradation","type":"exact"},{"name":"inhibition of toluene breakdown","type":"exact"},{"name":"inhibition of toluene catabolic process","type":"narrow"},{"name":"inhibition of toluene catabolism","type":"exact"},{"name":"inhibition of toluene degradation","type":"exact"},{"name":"negative regulation of toluene breakdown","type":"exact"},{"name":"negative regulation of toluene catabolism","type":"exact"},{"name":"negative regulation of toluene degradation","type":"exact"}],"termid":"GO:1901435"}


id: GO:1990517
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process in which a protein is transported to, or maintained in, a location within a photoreceptor outer segment, which is a portion of a modified sensory cilium.","definition_xrefs":["PMID:20212494","GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete protein localization to photoreceptor outer segment (obsolete GO:1990517)","termid":"GO:1990517"}


id: GO:0051515
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of monopolar cell growth, polarized growth from one end of a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of unidimensional cell growth","termid":"GO:0051512"},{"relation_name":"is_a","term_name":"regulation of monopolar cell growth","termid":"GO:0051513"},{"relation_name":"positively_regulates","term_name":"monopolar cell growth","termid":"GO:0042814"}],"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 monopolar cell growth","synonyms":[{"name":"stimulation of monopolar cell growth","type":"narrow"},{"name":"up regulation of monopolar cell growth","type":"exact"},{"name":"up-regulation of monopolar cell growth","type":"exact"},{"name":"upregulation of monopolar cell growth","type":"exact"}],"termid":"GO:0051515"}


id: PBO:0067111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 153, pseudogene","termid":"PBO:0067111"}


id: GO:0032780
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or reduces the rate of an ATP-dependent activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ATP-dependent activity","termid":"GO:0043462"},{"relation_name":"is_a","term_name":"negative regulation of molecular function","termid":"GO:0044092"}],"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 ATP-dependent activity","synonyms":[{"name":"down regulation of ATPase activity","type":"exact"},{"name":"down-regulation of ATPase activity","type":"exact"},{"name":"downregulation of ATPase activity","type":"exact"},{"name":"inhibition of ATPase activity","type":"narrow"},{"name":"negative regulation of ATPase activity","type":"exact"},{"name":"negative regulation of adenosinetriphosphatase activity","type":"exact"}],"termid":"GO:0032780"}


id: PBO:0068329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNF32 divergent transcript","termid":"PBO:0068329"}


id: MONDO:0009154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the NKX2-5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypothyroidism, congenital, nongoitrous","termid":"MONDO:0000045"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypothyroidism, congenital, nongoitrous, 5","secondary_identifiers":["OMIM:225250","MESH:C567123","DOID:0070125","UMLS:C2673630","GARD:15165","MEDGEN:388687"],"synonyms":[{"name":"CHNG5","type":"exact"},{"name":"NKX2-5 hypothyroidism, congenital, nongoitrous","type":"exact"},{"name":"congenital nongoitrous hypothyroidism 5","type":"related"},{"name":"hypothyroidism, congenital nongoitrous, 5","type":"exact"},{"name":"hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5","type":"exact"},{"name":"hypothyroidism, congenital, nongoitrous, 5","type":"exact"},{"name":"hypothyroidism, congenital, nongoitrous, type 5","type":"exact"}],"termid":"MONDO:0009154","xrefs":{"Monarch":{"xref_id":"0009154"}}}


id: PBO:0051815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 1 receptor associated kinase 1","termid":"PBO:0051815"}


id: PBO:0062016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily L member 6 pseudogene","termid":"PBO:0062016"}


id: MONDO:0001704
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that arises from the vagina and is characterized by the presence of neoplastic glandular epithelial cells. Representative examples include adenoma, endometrioid adenocarcinoma, and clear cell adenocarcinoma.","definition_xrefs":["NCIT:C40250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal neoplasm","termid":"MONDO:0021050"},{"relation_name":"is_a","term_name":"glandular cell neoplasm","termid":"MONDO:0024276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vaginal glandular neoplasm","secondary_identifiers":["DOID:134","MEDGEN:275574","UMLS:C1519921"],"synonyms":[{"name":"vagina glandular cell neoplasm","type":"exact"},{"name":"vaginal glandular neoplasm","type":"exact"},{"name":"vaginal glandular tumor","type":"exact"},{"name":"vaginal glandular tumour","type":"exact"}],"termid":"MONDO:0001704","xrefs":{"Monarch":{"xref_id":"0001704"}}}


id: PBO:0085265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peroxin; required for targeting of peroxisomal matrix proteins containing PTS2; interacts with Pex7p; partially redundant with Pex21p; primarily responsible for peroxisomal import during growth on oleate, and expression is induced during oleate growth","termid":"PBO:0085265"}


id: MONDO:0010960
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":"protocadherin 3","secondary_identifiers":["MEDGEN:371487","UMLS:C1833117","OMIM:600931"],"synonyms":[{"name":"Pcdh3","type":"related"},{"name":"protocadherin 3","type":"exact"},{"name":"protocadherin type 3","type":"exact"}],"termid":"MONDO:0010960","xrefs":{"Monarch":{"xref_id":"0010960"}}}


id: FYPO:0004335
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to another does not occur during a cellular response to hydrogen peroxide. The relevant proteins may include the one encoded by the mutated gene, or may both be encoded by different genes.","definition_xrefs":["PMID:22139357","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein-protein interaction during cellular response to rapamycin","termid":"FYPO:0003425"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000652","FYPO:0000702"],"is_obsolete":false,"name":"abolished protein-protein interaction during cellular response to hydrogen peroxide","synonyms":[{"name":"abolished protein binding cellular response to hydrogen peroxide","type":"exact"},{"name":"abolished protein-protein interaction during cellular response to H2O2","type":"exact"},{"name":"protein-protein interaction abolished during cellular response to hydrogen peroxide","type":"exact"}],"termid":"FYPO:0004335"}


id: PBO:0064447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"podocan","termid":"PBO:0064447"}


id: GO:0010942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the rate or frequency of cell death. Cell death is the specific activation or halting of processes within a cell so that its vital functions markedly cease, rather than simply deteriorating gradually over time, which culminates in cell death.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cell death (obsolete GO:0010942)","termid":"GO:0010942"}


id: GO:0140068
data:
  {"annotated_genes":["SJAG_02773","SJAG_02990"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90618,98163],"is_not":false,"summary":null,"term":"GO:0140068"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: crotonyl-CoA + histone = CoA + crotonyl-histone.","definition_xrefs":["PMID:25818647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide crotonyltransferase activity","termid":"GO:0140064"},{"relation_name":"is_a","term_name":"histone modifying activity","termid":"GO:0140993"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02773":null,"SJAG_02990":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016746","GO:0140096","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"histone crotonyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140068","terms_by_termid":{"GO:0140068":null}}


id: PBO:0052521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 34","termid":"PBO:0052521"}


id: GO:0017188
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-aspartate + acetyl-CoA = N-acetyl-L-aspartate + CoA + H+.","definition_xrefs":["RHEA:14165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetyltransferase activity","termid":"GO:0008080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016746","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"aspartate N-acetyltransferase activity","secondary_identifiers":["Reactome:R-HSA-8954468","KEGG_REACTION:R00487","EC:2.3.1.17","MetaCyc:ASPARTATE-N-ACETYLTRANSFERASE-RXN"],"synonyms":[{"name":"L-aspartate N-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:L-aspartate N-acetyltransferase activity","type":"related"},{"name":"aspartate acetyltransferase activity","type":"related"}],"termid":"GO:0017188"}


id: PBO:0082903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cys-Gly metallo-di-peptidase; forms a complex with Dug2p and Dug3p to degrade glutathione (GSH) and other peptides containing a gamma-glu-X bond in an alternative pathway to GSH degradation by gamma-glutamyl transpeptidase (Ecm38p); human homolog CNDP2 can complement yeast dug1 mutant","termid":"PBO:0082903"}


id: MONDO:0018863
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete leptospirosis (obsolete MONDO:0018863)","termid":"MONDO:0018863","xrefs":{"Monarch":{"xref_id":"0018863"}}}


id: PR:P40902
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- isp7 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P40902"],"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":"sexual differentiation process protein isp7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25B8.13c","synonyms":[{"name":"Spom972h-isp7","type":"exact"}],"termid":"PR:P40902"}


id: PBO:0025533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein, CENP-C ortholog Cnp3","termid":"PBO:0025533"}


id: PBO:0005388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper binding protein of the mitchondrial inner membrane Cmc2 (predicted)","termid":"PBO:0005388"}


id: MONDO:0006709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tumor or cancer of the common bile duct including the ampulla of vater and the sphincter of oddi.","definition_xrefs":["MESH:D003138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"common bile duct disorder","termid":"MONDO:0002886"},{"relation_name":"is_a","term_name":"extrahepatic bile duct neoplasm","termid":"MONDO:0021385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"common bile duct neoplasm","secondary_identifiers":["UMLS:C0009442","DOID:4608","SCTID:126857009","MEDGEN:3178"],"synonyms":[{"name":"common bile duct neoplasm (disease)","type":"exact"},{"name":"common bile duct tumor","type":"exact"},{"name":"common bile duct tumour","type":"exact"},{"name":"neoplasm of common bile duct","type":"exact"},{"name":"tumor of common bile duct","type":"exact"},{"name":"tumour of common bile duct","type":"exact"}],"termid":"MONDO:0006709","xrefs":{"Monarch":{"xref_id":"0006709"}}}


id: MONDO:1011646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent truncus arteriosus with ventricular septal defect and patent foramen ovale, non-human animal","secondary_identifiers":["OMIA:001218"],"termid":"MONDO:1011646","xrefs":{"Monarch":{"xref_id":"1011646"}}}


id: PATO:0000340
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000340 relative compatability value (obsolete PATO:0000340)","termid":"PATO:0000340"}


id: GO:0047256
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a beta-D-Gal-(1->4)-beta-D-Glc-(1<->1)-Cer(d18:1(4E)) + UDP-N-acetyl-alpha-D-glucosamine = a beta-D-GlcNAc-(1->3)-beta-D-Gal-(1->4)-beta-D-Glc-(1<->1)-Cer(d18:1(4E)) + H+ + UDP.","definition_xrefs":["RHEA:13905"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016757","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase activity","secondary_identifiers":["Reactome:R-HSA-9846501","MetaCyc:2.4.1.206-RXN","EC:2.4.1.206"],"synonyms":[{"name":"LA2 synthase activity","type":"related"},{"name":"UDP-N-acetyl-D-glucosamine:D-galactosyl-1,4-beta-D-glucosylceramide beta-1,3-acetylglucosaminyltransferase activity","type":"related"},{"name":"beta1->3-N-acetylglucosaminyltransferase activity","type":"related"},{"name":"lactosylceramide beta-acetylglucosaminyltransferase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-lactosylceramide beta-acetylglucosaminyltransferase activity","type":"related"}],"termid":"GO:0047256"}


id: GO:1904744
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of telomeric DNA binding.","definition_xrefs":["GOC:nc","GOC:TermGenie","PMID:24415760","GO_REF:0000059","GOC:BHF_telomere","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA binding","termid":"GO:0043388"},{"relation_name":"is_a","term_name":"regulation of telomeric DNA binding","termid":"GO:1904742"}],"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 telomeric DNA binding","synonyms":[{"name":"activation of telomere binding","type":"narrow"},{"name":"activation of telomeric DNA binding","type":"narrow"},{"name":"activation of telomeric repeat binding","type":"narrow"},{"name":"positive regulation of telomere binding","type":"exact"},{"name":"positive regulation of telomeric repeat binding","type":"exact"},{"name":"up regulation of telomere binding","type":"exact"},{"name":"up regulation of telomeric DNA binding","type":"exact"},{"name":"up regulation of telomeric repeat binding","type":"exact"},{"name":"up-regulation of telomere binding","type":"exact"},{"name":"up-regulation of telomeric DNA binding","type":"exact"},{"name":"up-regulation of telomeric repeat binding","type":"exact"},{"name":"upregulation of telomere binding","type":"exact"},{"name":"upregulation of telomeric DNA binding","type":"exact"},{"name":"upregulation of telomeric repeat binding","type":"exact"}],"termid":"GO:1904744"}


id: PBO:0057321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 519a-2","termid":"PBO:0057321"}


id: GO:1902969
data:
  {"annotated_genes":["SJAG_00247","SJAG_02690","SJAG_00863","SJAG_05197","SJAG_01823","SJAG_03451","SJAG_02908","SJAG_02162","SJAG_03160","SJAG_03843","SJAG_01068","SJAG_04183","SJAG_01354","SJAG_03898","SJAG_00874","SJAG_01677","SJAG_02439","SJAG_02294","SJAG_02172","SJAG_00729","SJAG_00536","SJAG_02667","SJAG_02198","SJAG_05239","SJAG_04995","SJAG_01210","SJAG_01221","SJAG_02822","SJAG_02079","SJAG_00884","SJAG_03780","SJAG_04877","SJAG_00272","SJAG_02074","SJAG_05232","SJAG_00573","SJAG_00198","SJAG_01762","SJAG_04341","SJAG_00327","SJAG_02199","SJAG_00857","SJAG_00814","SJAG_02607","SJAG_00618","SJAG_02348","SJAG_06022","SJAG_02182","SJAG_04671","SJAG_04272","SJAG_01010","SJAG_04879","SJAG_03048","SJAG_01884","SJAG_01374","SJAG_03695","SJAG_00400","SJAG_02992","SJAG_01832","SJAG_01076","SJAG_02818","SJAG_04190","SJAG_04210","SJAG_03495","SJAG_01410"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105586],"is_not":false,"summary":null,"term":"GO:1902969"},{"annotations":[106507,114541,112288,111651,102006,94429,93158,111411,103399,88782,109098,112698,106141,108259,104093,94463],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902983"},{"annotations":[106406,109370,92188,98552,110529,112289,106508,98615,114412,114543,93749,91160,109702,114241,105587,116467,96624],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902975"},{"annotations":[94431,102008,103403,108261,117309,104095],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903459"},{"annotations":[94464,104096,106142,103404,88783,93160,94432,106509],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903460"},{"annotations":[108276,110901],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990505"},{"annotations":[109703,89653,98616],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902977"},{"annotations":[102498,109704,114154],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902985"},{"annotations":[106889,106913,95372,108708,111653,97445,95209,88375,108233,90157,94266,98258,115937,94024,98144],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990426"},{"annotations":[115983,108041],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903464"},{"annotations":[101552,108042,96965],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903467"},{"annotations":[100687,99796,103329,94253,99832,91851,91762],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903461"},{"annotations":[116406,102499,111178],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903468"},{"annotations":[101562],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903465"},{"annotations":[87515,103330,102126,111654],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903469"}]},"cv_name":"biological_process","definition":"Any nuclear DNA replication that is involved in a mitotic cell cycle.","definition_xrefs":["GOC:TermGenie","GO_REF:0000060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear DNA replication","termid":"GO:0033260"},{"relation_name":"is_a","term_name":"mitotic cell cycle 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DNA replication","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA replication during S phase involved in mitotic cell cycle","type":"related"},{"name":"DNA replication involved in S phase involved in mitotic cell cycle","type":"exact"},{"name":"DNA replication involved in S-phase involved in mitotic cell cycle","type":"exact"},{"name":"mitotic cell cycle DNA replication","type":"exact"},{"name":"mitotic nuclear cell cycle DNA replication","type":"exact"},{"name":"nuclear cell cycle DNA replication involved in mitotic cell cycle","type":"related"}],"termid":"GO:1902969","terms_by_termid":{"GO:1902969":null,"GO:1902975":null,"GO:1902977":null,"GO:1902983":null,"GO:1902985":null,"GO:1903459":null,"GO:1903460":null,"GO:1903461":null,"GO:1903464":null,"GO:1903465":null,"GO:1903467":null,"GO:1903468":null,"GO:1903469":null,"GO:1990426":null,"GO:1990505":null}}


id: PBO:0071578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35 pseudogene 7","termid":"PBO:0071578"}


id: MONDO:0957274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"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":"spastic paraplegia 89, autosomal recessive","secondary_identifiers":["OMIM:620379","MEDGEN:1841167","UMLS:C5830531","DOID:0070458"],"termid":"MONDO:0957274","xrefs":{"Monarch":{"xref_id":"0957274"}}}


id: GO:0001818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of production of a cytokine.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"is_a","term_name":"negative regulation of gene expression","termid":"GO:0010629"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of cytokine production","secondary_identifiers":["GO:0042036","GO:0050710"],"synonyms":[{"name":"down regulation of cytokine biosynthetic process","type":"exact"},{"name":"down regulation of cytokine production","type":"exact"},{"name":"down-regulation of cytokine biosynthetic process","type":"exact"},{"name":"down-regulation of cytokine production","type":"exact"},{"name":"downregulation of cytokine biosynthetic process","type":"exact"},{"name":"downregulation of cytokine production","type":"exact"},{"name":"inhibition of cytokine biosynthetic process","type":"narrow"},{"name":"inhibition of cytokine production","type":"narrow"},{"name":"negative regulation of cytokine anabolism","type":"exact"},{"name":"negative regulation of cytokine biosynthesis","type":"exact"},{"name":"negative regulation of cytokine biosynthetic process","type":"narrow"},{"name":"negative regulation of cytokine formation","type":"exact"},{"name":"negative regulation of cytokine secretion","type":"narrow"},{"name":"negative regulation of cytokine synthesis","type":"exact"}],"termid":"GO:0001818"}


id: GO:0047994
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-hydroxy-3-methylglutaryl-CoA + H2O = 3-hydroxy-3-methylglutarate + CoA + H+.","definition_xrefs":["RHEA:16305","EC:3.1.2.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA hydrolase activity","termid":"GO:0016289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"hydroxymethylglutaryl-CoA hydrolase activity","secondary_identifiers":["KEGG_REACTION:R02083","MetaCyc:HYDROXYMETHYLGLUTARYL-COA-HYDROLASE-RXN"],"synonyms":[{"name":"(S)-3-hydroxy-3-methylglutaryl-CoA hydrolase activity","type":"related"},{"name":"3-hydroxy-3-methylglutaryl-CoA hydrolase activity","type":"related"},{"name":"beta-hydroxy-beta-methylglutaryl coenzyme A deacylase activity","type":"related"},{"name":"beta-hydroxy-beta-methylglutaryl coenzyme A hydrolase activity","type":"related"},{"name":"hydroxymethylglutaryl coenzyme A deacylase activity","type":"related"},{"name":"hydroxymethylglutaryl coenzyme A hydrolase activity","type":"related"}],"termid":"GO:0047994"}


id: PBO:0064506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit G","termid":"PBO:0064506"}


id: FYPO:0006628
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of phosphatidylinositol-4-phosphate measured in the plasma membrane is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased phosphatidylinositol phosphate level in plasma membrane","termid":"FYPO:0006222"},{"relation_name":"is_a","term_name":"decreased cellular phosphatidylinositol-4-phosphate level","termid":"FYPO:0006775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased phosphatidylinositol-4-phosphate level in plasma membrane","synonyms":[{"name":"decreased 1-phosphatidyl-1D-myo-inositol 4-phosphate level in plasma membrane","type":"exact"},{"name":"decreased phosphatidylinositol-4-phosphate level in cell membrane","type":"exact"},{"name":"decreased phosphatidylinositol-4-phosphate level in plasma membrane during mitotic cell cycle","type":"related"},{"name":"decreased phosphatidylinositol-4-phosphate level in plasma membrane during vegetative growth","type":"exact"},{"name":"decreased plasma membrane PI(5)P level","type":"exact"},{"name":"decreased plasma membrane phosphatidylinositol-4-phosphate level","type":"exact"},{"name":"reduced phosphatidylinositol-4-phosphate level in plasma membrane","type":"exact"}],"termid":"FYPO:0006628"}


id: MONDO:0007835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Telescoping or invagination of a part of the intestine into an adjacent segment.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"intestinal obstruction","termid":"MONDO:0004565"}],"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":"intussusception","secondary_identifiers":["DOID:8446","UMLS:C0021933","OMIM:147710","ICD10CM:K56.1","ICD9:560.0","SCTID:49723003","MESH:D007443","MEDGEN:43940"],"synonyms":[{"name":"intussusception","type":"exact"},{"name":"intussusception (morphologic abnormality)","type":"exact"},{"name":"intussusception of intestine","type":"exact"},{"name":"invagination of intestine or colon","type":"exact"}],"termid":"MONDO:0007835","xrefs":{"Monarch":{"xref_id":"0007835"}}}


id: PBO:0018108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi to ER protein (predicted)","termid":"PBO:0018108"}


id: PBO:0045118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DMRT like family A2","termid":"PBO:0045118"}


id: MONDO:1011431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gaucher disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease, non-human animal","termid":"MONDO:1010171"},{"relation_name":"is_a","term_name":"disorder of orbital region, non-human animal","termid":"MONDO:1011315"},{"relation_name":"is_a","term_name":"disorder of visual system, non-human animal","termid":"MONDO:1011316"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gaucher disease, non-human animal","secondary_identifiers":["OMIA:000405"],"termid":"MONDO:1011431","xrefs":{"Monarch":{"xref_id":"1011431"}}}


id: PBO:0054006
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 1335","termid":"PBO:0054006"}


id: GO:0051181
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a cofactor into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. A cofactor is a substance that is required for the activity of an enzyme or other protein.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cofactor transport (obsolete GO:0051181)","synonyms":[{"name":"vitamin or cofactor transport","type":"broad"}],"termid":"GO:0051181"}


id: MONDO:0013485
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 35 (SCA35) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, intention tremor, hyperreflexia and spasmodic torticollis.","definition_xrefs":["Orphanet:276193"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type I","termid":"MONDO:0019792"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039","MONDO:0000426"],"is_obsolete":false,"name":"spinocerebellar ataxia type 35","secondary_identifiers":["DOID:0050982","GARD:12366","icd11.foundation:1674449075","MEDGEN:854733","OMIM:613908","SCTID:719300001","UMLS:C3888031"],"synonyms":[{"name":"SCA35","type":"exact"},{"name":"spinocerebellar ataxia 35","type":"related"},{"name":"spinocerebellar ataxia type 35","type":"exact"}],"termid":"MONDO:0013485","xrefs":{"Monarch":{"xref_id":"0013485"}}}


id: PBO:0005904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Glutamic acid, mitochondrial","termid":"PBO:0005904"}


id: PBO:0056384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase 14","termid":"PBO:0056384"}


id: PBO:0002284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome component alpha 5, Pup2 (predicted)","termid":"PBO:0002284"}


id: MONDO:0000958
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuroretinitis is an inflammation of the neural retina and optic nerve. Pathology: Direct invasion or autoimmune activation against the optic nerve may cause optic nerve vascular inflammation with secondary inflammation and edema in the nerve fiber layer of the retina.","direct_ancestors":[{"relation_name":"is_a","term_name":"neuritis","termid":"MONDO:0002122"},{"relation_name":"is_a","term_name":"retinal nerve fiber layer disorder","termid":"MONDO:0003579"},{"relation_name":"is_a","term_name":"optic papillitis","termid":"MONDO:0006879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005244"],"is_obsolete":false,"name":"neuroretinitis","secondary_identifiers":["DOID:10176","icd11.foundation:418437487","MEDGEN:57826","ICD9:363.05","MESH:D012173","UMLS:C0154874"],"synonyms":[{"name":"Juxtapapillary focal retinitis and retinochoroiditis","type":"narrow"},{"name":"focal retinitis and retinochoroiditis, juxtapapillary","type":"narrow"},{"name":"papilloretinitis","type":"narrow"}],"termid":"MONDO:0000958","xrefs":{"Monarch":{"xref_id":"0000958"}}}


id: MONDO:0035408
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"furuncular myiasis","termid":"MONDO:0018941"}],"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":"furuncular myiasis due to Cordylobia rodhaini","secondary_identifiers":["UMLS:C5231033","GARD:22261","ICD10CM:B87.0","MEDGEN:1685143","Orphanet:563690"],"synonyms":[{"name":"furunculoid myiasis due to Cordylobia rodhaini","type":"exact"},{"name":"furunculous myiasis due to Cordylobia rodhaini","type":"exact"}],"termid":"MONDO:0035408","xrefs":{"Monarch":{"xref_id":"0035408"}}}


id: MOD:01909
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a residue to the 6x(13)C labeled 4-sulfophenyl isothiocyanate adduct, alpha-amino-[(4-sulfophenyl)carbamothioyl] residue.","definition_xrefs":["Unimod:464#N-term","PubMed:16526082","PubMed:11467524"],"direct_ancestors":[{"relation_name":"is_a","term_name":"6x(13)C labeled 4-sulfophenyl isothiocyanate derivatized residue","termid":"MOD:00880"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C labeled 4-sulfophenyl isothiocyanate alpha-amino derivatized residue","synonyms":[{"name":"4-sulfophenyl isothiocyanate (Heavy C13)","type":"related"},{"name":"SPITC:13C(6)","type":"related"}],"termid":"MOD:01909"}


id: GO:1905959
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cellular response to alcohol.","definition_xrefs":["PMID:26434723","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of response to alcohol","termid":"GO:1901421"},{"relation_name":"is_a","term_name":"regulation of cellular response to alcohol","termid":"GO:1905957"},{"relation_name":"positively_regulates","term_name":"cellular response to alcohol","termid":"GO:0097306"}],"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 cellular response to alcohol","synonyms":[{"name":"activation of cellular response to alcohol","type":"narrow"},{"name":"up regulation of cellular response to alcohol","type":"exact"},{"name":"up-regulation of cellular response to alcohol","type":"exact"},{"name":"upregulation of cellular response to alcohol","type":"exact"}],"termid":"GO:1905959"}


id: PBO:0069637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 914, pseudogene","termid":"PBO:0069637"}


id: GO:0106141
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dimethylallyl phosphate + FMNH2 = phosphate + prenyl-FMNH2.","definition_xrefs":["PMID:26083743","RHEA:37743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenyltransferase activity","termid":"GO:0004659"}],"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:0016765"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016765"],"is_obsolete":false,"name":"flavin prenyltransferase activity","secondary_identifiers":["EC:2.5.1.129"],"termid":"GO:0106141"}


id: MONDO:0958190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bradyopsia","termid":"MONDO:0012033"}],"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":"prolonged electroretinal response suppression 2","secondary_identifiers":["DOID:0070364","MEDGEN:1841088","UMLS:C5830452","OMIM:620344"],"termid":"MONDO:0958190","xrefs":{"Monarch":{"xref_id":"0958190"}}}


id: GO:0070447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the rate or extent of oligodendrocyte progenitor proliferation.","definition_xrefs":["GOC:mah","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of gliogenesis","termid":"GO:0014015"},{"relation_name":"is_a","term_name":"regulation of oligodendrocyte progenitor proliferation","termid":"GO:0070445"},{"relation_name":"is_a","term_name":"positive regulation of neural precursor cell proliferation","termid":"GO:2000179"},{"relation_name":"positively_regulates","term_name":"oligodendrocyte progenitor proliferation","termid":"GO:0070444"}],"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 oligodendrocyte progenitor proliferation","synonyms":[{"name":"positive regulation of oligodendrocyte precursor proliferation","type":"exact"}],"termid":"GO:0070447"}


id: GO:0033713
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: choline + O2 = betaine aldehyde + hydrogen peroxide.","definition_xrefs":["EC:1.1.3.17","RHEA:13505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"choline:oxygen 1-oxidoreductase activity","secondary_identifiers":["MetaCyc:CHOLINE-OXIDASE-RXN"],"synonyms":[{"name":"choline oxidase activity","type":"broad"}],"termid":"GO:0033713"}


id: GO:0050426
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H2O + peptidyl-glycinamide = glycinamide + peptide. Cleavage of C-terminal glycinamide from a polypeptide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-glycinamidase activity (obsolete GO:0050426)","synonyms":[{"name":"peptidyl-glycinamidase activity","type":"exact"}],"termid":"GO:0050426"}


id: GO:0042402
data:
  {"annotated_genes":["SJAG_03288"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[86624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009447"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways occurring at the level of individual cells resulting in the breakdown of biogenic amines, any of a group of naturally occurring, biologically active amines, such as norepinephrine, histamine, and serotonin, many of which act as neurotransmitters.","definition_xrefs":["GOC:go_curators","GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amine catabolic process","termid":"GO:0009310"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03288":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"biogenic amine catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"biogenic amine breakdown","type":"exact"},{"name":"biogenic amine catabolism","type":"exact"},{"name":"biogenic amine degradation","type":"exact"}],"termid":"GO:0042402","terms_by_termid":{"GO:0009447":null}}


id: PBO:0012529
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-results_in_formation_of","termid":"PBO:0012529"}


id: PBO:0062517
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 K member 3 (gene/pseudogene)","termid":"PBO:0062517"}


id: GO:0014813
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a satellite cell.","definition_xrefs":["GOC:ef","GOC:mtg_muscle","PMID:16607119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate commitment","termid":"GO:0045165"},{"relation_name":"part_of","term_name":"skeletal muscle satellite cell differentiation","termid":"GO:0014816"}],"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":"skeletal muscle satellite cell commitment","termid":"GO:0014813"}


id: GO:1900053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of retinoic acid biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hormone metabolic process","termid":"GO:0032351"},{"relation_name":"is_a","term_name":"negative regulation of isoprenoid metabolic process","termid":"GO:0045827"},{"relation_name":"is_a","term_name":"negative regulation of vitamin metabolic process","termid":"GO:0046137"},{"relation_name":"is_a","term_name":"negative regulation of lipid biosynthetic process","termid":"GO:0051055"},{"relation_name":"is_a","term_name":"regulation of retinoic acid biosynthetic process","termid":"GO:1900052"},{"relation_name":"negatively_regulates","term_name":"retinoic acid biosynthetic process","termid":"GO:0002138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006766"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006766"}],"interesting_parent_ids":["GO:0044281","GO:0006766","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of retinoic acid biosynthetic process","synonyms":[{"name":"down regulation of retinoic acid anabolic process","type":"exact"},{"name":"down regulation of retinoic acid biosynthetic process","type":"related"},{"name":"down-regulation of retinoic acid anabolic process","type":"exact"},{"name":"down-regulation of retinoic acid biosynthetic process","type":"related"},{"name":"downregulation of retinoic acid anabolic process","type":"exact"},{"name":"downregulation of retinoic acid biosynthetic process","type":"related"},{"name":"inhibition of retinoic acid anabolic process","type":"exact"},{"name":"inhibition of retinoic acid biosynthetic process","type":"related"},{"name":"negative regulation of retinoic acid anabolic process","type":"exact"}],"termid":"GO:1900053"}


id: FYPO:0007111
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which microtubule depolymerization, i.e. the removal of tubulin dimers from a microtubule, is abnormal.","definition_xrefs":["PomBase:mah","GO:0007019"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton organization","termid":"FYPO:0000054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000054"],"is_obsolete":false,"name":"abnormal microtubule depolymerization","synonyms":[{"name":"abnormal microtubule catastrophe","type":"related"},{"name":"abnormal microtubule depolymerisation","type":"exact"},{"name":"abnormal microtubule shrinkage","type":"related"}],"termid":"FYPO:0007111"}


id: PBO:0072045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 15","termid":"PBO:0072045"}


id: GO:0043673
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The outer, sculptured layer of the exine, which lies above the nexine.","definition_xrefs":["PMID:5722147"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"exine","termid":"GO:0043668"}],"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":"sexine","termid":"GO:0043673"}


id: PBO:0057977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3692","termid":"PBO:0057977"}


id: MONDO:0013656
data:
  {"annotated_genes":["SJAG_00773"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85062],"is_not":false,"summary":null,"term":"MONDO:0013656"}]},"cv_name":"mondo","definition":"An autosomal dominant condition caused by mutation(s) in the KIF1A gene, encoding kinesin-like protein KIF1A. It is characterized by microcephaly, intellectual disability, and delayed psychomotor development. The condition is progressive, occurs in early infancy, and is of variable severity.","definition_xrefs":["NCIT:C133742"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intellectual disability, autosomal dominant","termid":"MONDO:0100172"},{"relation_name":"is_a","term_name":"KIF1A related neurological disorder","termid":"MONDO:0700055"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00773":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual disability, autosomal dominant 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5393830","DOID:0070039","MEDGEN:1714250","OMIM:614255","Orphanet:662367","GARD:16459"],"synonyms":[{"name":"KIF1A autosomal dominant non-syndromic intellectual disability","type":"exact"},{"name":"MRD9","type":"exact"},{"name":"NESCAV syndrome","type":"exact"},{"name":"autosomal dominant intellectual disability 9","type":"exact"},{"name":"autosomal dominant mental retardation 9","type":"exact"},{"name":"autosomal dominant non-syndromic intellectual disability 9","type":"related"},{"name":"autosomal dominant non-syndromic intellectual disability caused by mutation in KIF1A","type":"exact"},{"name":"intellectual disability, autosomal dominant 9","type":"exact"},{"name":"intellectual disability, autosomal dominant type 9","type":"exact"},{"name":"mental retardation, autosomal dominant 9","type":"related"},{"name":"mental retardation, autosomal dominant type 9","type":"exact"}],"termid":"MONDO:0013656","terms_by_termid":{"MONDO:0013656":null},"xrefs":{"Monarch":{"xref_id":"0013656"}}}


id: FYPO:0000633
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to G418. Cells stop growing (and may die) at a concentration of G418 that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0005447","FYPO:0001985","FYPO:0000003","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to G418","synonyms":[{"name":"hypersensitive to G418","type":"exact"},{"name":"sensitive to G418 during mitotic cell cycle","type":"related"},{"name":"sensitive to G418 during vegetative growth","type":"exact"},{"name":"sensitive to Geneticin","type":"exact"}],"termid":"FYPO:0000633"}


id: PBO:0064022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 56","termid":"PBO:0064022"}


id: GO:1904525
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of DNA amplification.","definition_xrefs":["PMID:26195783","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA amplification","termid":"GO:1904523"},{"relation_name":"is_a","term_name":"positive regulation of DNA biosynthetic process","termid":"GO:2000573"},{"relation_name":"positively_regulates","term_name":"DNA amplification","termid":"GO:0006277"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"positively_regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"positive regulation of DNA amplification","synonyms":[{"name":"activation of DNA amplification","type":"narrow"},{"name":"up regulation of DNA amplification","type":"exact"},{"name":"up-regulation of DNA amplification","type":"exact"},{"name":"upregulation of DNA amplification","type":"exact"}],"termid":"GO:1904525"}


id: PBO:0053850
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 1119","termid":"PBO:0053850"}


id: PBO:0011129
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AAA ATPase Like Fidgetin","termid":"PBO:0011129"}


id: GO:0015749
data:
  {"annotated_genes":["SJAG_03608","SJAG_03820","SJAG_00057"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109788,113307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046323"},{"annotations":[113308,116340],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098708"},{"annotations":[109789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140425"},{"annotations":[102159],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008645"}]},"cv_name":"biological_process","definition":"The process in which a monosaccharide is transported across a lipid bilayer, from one side of a membrane to the other. Monosaccharides are the simplest carbohydrates; they are polyhydric alcohols containing either an aldehyde or a keto group and between three to ten or more carbon atoms. They form the constitutional repeating units of oligo- and polysaccharides.","definition_xrefs":["GO_REF:0000069","GOC:TermGenie","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transmembrane transport","termid":"GO:0034219"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00057":null,"SJAG_03608":null,"SJAG_03820":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"monosaccharide transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1905950"],"synonyms":[{"name":"monosaccharide transport","type":"related"}],"termid":"GO:0015749","terms_by_termid":{"GO:0008645":null,"GO:0046323":null,"GO:0098708":null,"GO:0140425":null}}


id: GO:0070029
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphav-beta3 integrin complex bound to osteopontin.","definition_xrefs":["PMID:7532190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"alphav-beta3 integrin-osteopontin complex","synonyms":[{"name":"ITGAV-ITGB3-SPP1 complex","type":"narrow"}],"termid":"GO:0070029"}


id: MONDO:0016148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete qualitative or quantitative defects of collagen 6 (obsolete MONDO:0016148)","termid":"MONDO:0016148","xrefs":{"Monarch":{"xref_id":"0016148"}}}


id: SO:0000737
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"DNA belonging to the genome of a mitochondria.","direct_ancestors":[{"relation_name":"is_a","term_name":"organelle_sequence","termid":"SO:0000736"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial_sequence","synonyms":[{"name":"mitochondrial sequence","type":"exact"}],"termid":"SO:0000737"}


id: FYPO:0007895
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 ubiquitination of lysine at position 119 of histone H2B is increased at pericentromeric heterochromatin. Lysine 119 corresponds to the conserved C-terminal lysine of H2B.","definition_xrefs":["PMID:34731638"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein ubiquitination during vegetative growth","termid":"FYPO:0002082"},{"relation_name":"is_a","term_name":"abnormal histone H2B-K119 ubiquitination during vegetative growth","termid":"FYPO:0005607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002494","FYPO:0001320","FYPO:0001985","FYPO:0002274","FYPO:0000002"],"is_obsolete":false,"name":"increased histone H2B-K119 ubiquitination at pericentromeric heterochromatin","termid":"FYPO:0007895"}


id: PBO:0047198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 216 member A","termid":"PBO:0047198"}


id: GO:0022001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency or rate at which a cell adopts an anterior neural cell fate.","definition_xrefs":["GO_REF:0000021","GOC:jid","GOC:tb","GOC:dgh","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate commitment","termid":"GO:0010454"},{"relation_name":"is_a","term_name":"negative regulation of nervous system development","termid":"GO:0051961"},{"relation_name":"part_of","term_name":"neural plate anterior/posterior regionalization","termid":"GO:0021999"}],"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 anterior neural cell fate commitment of the neural plate","synonyms":[{"name":"caudalization of neural plate","type":"exact"},{"name":"down regulation of anterior neural cell fate of the neural plate","type":"exact"},{"name":"down-regulation of anterior neural cell fate of the neural plate","type":"exact"},{"name":"downregulation of anterior neural cell fate of the neural plate","type":"exact"},{"name":"inhibition of anterior neural cell fate of the neural plate","type":"narrow"},{"name":"negative regulation of anterior neural cell fate of the neural plate","type":"exact"},{"name":"posteriorization","type":"broad"}],"termid":"GO:0022001"}


id: GO:0060117
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an auditory receptor cell over time, from its formation to the mature structure. Cell development does not include the steps involved in committing a cell to a specific fate.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner ear receptor cell development","termid":"GO:0060119"},{"relation_name":"part_of","term_name":"inner ear auditory receptor cell differentiation","termid":"GO:0042491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"auditory receptor cell development","synonyms":[{"name":"auditory hair cell development","type":"exact"}],"termid":"GO:0060117"}


id: PBO:0084930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA-binding protein of the PUF family; binds to specific mRNAs, often in the 3' UTR; has broad specificity and binds to more than 1000 mRNAs (16% of the transcriptome); recruits the CCR4-NOT deadenylase complex to mRNAs along with Dhh1p and Dcp1p to promote deadenylation, decapping, and decay; also interacts with the Caf20p translational initiation repressor, affecting its mRNA target specificity","termid":"PBO:0084930"}


id: GO:1901823
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of delta-carotene.","definition_xrefs":["GOC:TermGenie","GOC:yaf","MetaCyc:PWY-5946","PMID:8837512","UniPathway:UPA00801"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid catabolic process","termid":"GO:0016118"},{"relation_name":"is_a","term_name":"carotene catabolic process","termid":"GO:0016121"},{"relation_name":"is_a","term_name":"delta-carotene metabolic process","termid":"GO:1901822"}],"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:0008150","GO:0006629"],"is_obsolete":false,"name":"delta-carotene catabolic process","synonyms":[{"name":"delta-carotene breakdown","type":"exact"},{"name":"delta-carotene catabolism","type":"exact"},{"name":"delta-carotene degradation","type":"exact"}],"termid":"GO:1901823"}


id: PBO:0059789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 15","termid":"PBO:0059789"}


id: PBO:0061021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 4","termid":"PBO:0061021"}


id: MONDO:0004795
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the anatomical structures of the outer ear and ear canal secondary to an infectious process. Bacterial etiology is most common, but fungal infection is also possible. Symptoms include erythema, edema, and pain.","definition_xrefs":["NCIT:C3299"],"direct_ancestors":[{"relation_name":"is_a","term_name":"external ear disorder","termid":"MONDO:0002776"},{"relation_name":"is_a","term_name":"ear infection","termid":"MONDO:0021666"},{"relation_name":"is_a","term_name":"post-infectious disorder","termid":"MONDO:0021669"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otitis externa","secondary_identifiers":["EFO:0009560","ICD9:380.1","DOID:9463","ICD10CM:H60","MESH:D010032","MEDGEN:10505","NCIT:C79601","SCTID:3135009","UMLS:C0029878","icd11.foundation:1303990434","ICD9:380.10"],"synonyms":[{"name":"external Ear infection","type":"exact"},{"name":"infectious otitis externa","type":"exact"},{"name":"otitis externa","type":"exact"},{"name":"outer Ear infection","type":"exact"},{"name":"swimmer's Ear","type":"exact"},{"name":"swimmer's ear","type":"exact"}],"termid":"MONDO:0004795","xrefs":{"Monarch":{"xref_id":"0004795"}}}


id: RO:0002433
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"p contributes to morphology of w if and only if a change in the morphology of p entails a change in the morphology of w. Examples: every skull contributes to morphology of the head which it is a part of. Counter-example: nuclei do not generally contribute to the morphology of the cell they are part of, as they are buffered by cytoplasm.","direct_ancestors":[{"relation_name":"is_a","term_name":"overlaps","termid":"RO:0002131"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contributes_to_morphology_of","termid":"RO:0002433"}


id: MONDO:0000205
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete radioulnar synostosis with amegakaryocytic thrombocytopenia (obsolete MONDO:0000205)","termid":"MONDO:0000205","xrefs":{"Monarch":{"xref_id":"0000205"}}}


id: PBO:0034428
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_iron_ion_starvation-induced_proteins_during_glutathione_starvation","termid":"PBO:0034428"}


id: FYPO:0000707
data:
  {"alleles_by_uniquename":{"SJAG_02796:allele-1":{"allele_type":"amino_acid_mutation","description":"A343T","gene_uniquename":"SJAG_02796","name":"pyk1-A343T","uniquename":"SJAG_02796:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007363"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a specific molecular function is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular function phenotype","termid":"FYPO:0000652"},{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02796":null},"genotype_count":1,"genotypes_by_uniquename":{"pyk1-A343T-A343T-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pyk1-A343T(aa)","display_uniquename":"pyk1-A343T-A343T-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02796:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652"],"is_obsolete":false,"name":"abnormal molecular function","references_by_uniquename":{"PMID:37164017":null},"single_locus_annotated_genes":["SJAG_02796"],"single_locus_genotype_uniquenames":["pyk1-A343T-A343T-amino_acid_mutation-expression-not_assayed_or_wild_type"],"termid":"FYPO:0000707","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYPO:0007363":null,"FYPO_EXT:0000002":null}}


id: GO:0071131
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaV-beta3 integrin complex bound to laminin alpha-4.","definition_xrefs":["PMID:16824487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"alphaV-beta3 integrin-laminin alpha-4 complex","synonyms":[{"name":"ITGAV-ITGB3-LAMA4 complex","type":"narrow"}],"termid":"GO:0071131"}


id: PBO:0051762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"importin 7 pseudogene 1","termid":"PBO:0051762"}


id: GO:0032623
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-2 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-2 production","secondary_identifiers":["GO:0042094","GO:0070970"],"synonyms":[{"name":"IL-2 production","type":"exact"},{"name":"interleukin-2 biosynthetic process","type":"narrow"},{"name":"interleukin-2 secretion","type":"narrow"}],"termid":"GO:0032623"}


id: GO:0006096
data:
  {"annotated_genes":["SJAG_01310","SJAG_02945","SJAG_00605","SJAG_04495","SJAG_03660","SJAG_03828","SJAG_06621","SJAG_03373","SJAG_04334","SJAG_00685","SJAG_05314","SJAG_00461","SJAG_02785","SJAG_02107","SJAG_03852","SJAG_02369","SJAG_02135","SJAG_04192","SJAG_04048","SJAG_02009","SJAG_06622","SJAG_00633","SJAG_03903","SJAG_02796","SJAG_00839","SJAG_00027"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103643],"is_not":false,"summary":null,"term":"GO:0006096"},{"annotations":[108546,108540,102818,104987,108077,108081,108082,94210,103641,104618,108079,108541,108542,108545,97188,104617,104616,97466,108076,108078,93723,102562,108080,108543,108544,115486,104986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"},{"annotations":[87818],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061613"},{"annotations":[97384,110719],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061688"},{"annotations":[72412,75326],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0045820"},{"annotations":[88421],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006110"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a carbohydrate into pyruvate, with the concomitant production of a small amount of ATP and the reduction of NAD(P) to NAD(P)H. Glycolysis begins with the metabolism of a carbohydrate to generate products that can enter the pathway and ends with the production of pyruvate. Pyruvate may be converted to acetyl-coenzyme A, ethanol, lactate, or other small molecules.","definition_xrefs":["ISBN:0201090910","ISBN:0716720094","ISBN:0879010479","Wikipedia:Glycolysis","GOC:bf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate metabolic process","termid":"GO:0006090"},{"relation_name":"is_a","term_name":"generation of precursor metabolites and energy","termid":"GO:0006091"},{"relation_name":"is_a","term_name":"carbohydrate catabolic process","termid":"GO:0016052"},{"relation_name":"is_a","term_name":"pyridine nucleotide catabolic process","termid":"GO:0019364"},{"relation_name":"is_a","term_name":"ADP catabolic process","termid":"GO:0046032"},{"relation_name":"is_a","term_name":"ATP metabolic process","termid":"GO:0046034"},{"relation_name":"is_a","term_name":"nicotinamide nucleotide metabolic process","termid":"GO:0046496"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00461":null,"SJAG_00605":null,"SJAG_00633":null,"SJAG_00685":null,"SJAG_00839":null,"SJAG_01310":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02369":null,"SJAG_02785":null,"SJAG_02796":null,"SJAG_02945":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03828":null,"SJAG_03852":null,"SJAG_03903":null,"SJAG_04048":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_05314":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0005975","GO:0044281","GO:0006091","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"glycolytic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0019641","GO:0019642","MetaCyc:GLYCOLYSIS-VARIANTS"],"synonyms":[{"name":"Embden-Meyerhof pathway","type":"related"},{"name":"Embden-Meyerhof-Parnas pathway","type":"related"},{"name":"anaerobic glycolysis","type":"related"},{"name":"glycolysis","type":"related"},{"name":"modified Embden-Meyerhof pathway","type":"related"}],"termid":"GO:0006096","terms_by_termid":{"GO:0006096":null,"GO:0006110":null,"GO:0045820":null,"GO:0061613":null,"GO:0061621":null,"GO:0061688":null}}


id: PBO:0063794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHD finger protein 21B","termid":"PBO:0063794"}


id: PBO:0049024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 3","termid":"PBO:0049024"}


id: PBO:0049439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GUSB pseudogene 16","termid":"PBO:0049439"}


id: MONDO:0020368
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Axenfeld's anomaly is a rare congenital ocular defect caused by anterior segment dysgenesis and is characterized by anteriorly displaced Schwalbe's line and iris bands extending into the cornea. In contrast, Rieger's anomaly includes characteristic iris and pupil anomalies.","definition_xrefs":["Orphanet:98978"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete goniodysgenesis (obsolete MONDO:0020218)","termid":"MONDO:0020218"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"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":"Axenfeld anomaly","secondary_identifiers":["ICD9:743.44","SCTID:204152008","icd11.foundation:1703498511","MedDRA:10058653","UMLS:C0266548","GARD:16485","MEDGEN:78611"],"termid":"MONDO:0020368","xrefs":{"Monarch":{"xref_id":"0020368"}}}


id: PBO:0079897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome c reductase complex assembly factor 6","termid":"PBO:0079897"}


id: MONDO:0024516
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of hidradenitis suppurativa that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hidradenitis suppurativa","termid":"MONDO:0006559"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"familial acne inversa","secondary_identifiers":["OMIMPS:142690","UMLS:C1840560","MEDGEN:326766"],"synonyms":[{"name":"ACNINV","type":"exact"},{"name":"familial hidradenitis suppurativa","type":"exact"},{"name":"hereditary hidradenitis suppurativa","type":"exact"}],"termid":"MONDO:0024516","xrefs":{"Monarch":{"xref_id":"0024516"}}}


id: GO:0008999
data:
  {"annotated_genes":["SJAG_04631"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88604],"is_not":false,"summary":null,"term":"GO:0008999"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + N-terminal L-alanyl-[protein] = CoA + H+ + N-terminal N(alpha)-acetyl-L-alanyl-[protein].","definition_xrefs":["RHEA:50500"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide alpha-N-acetyltransferase activity","termid":"GO:0004596"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04631":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0034212"}],"interesting_parent_ids":["GO:0003674","GO:0034212","GO:0016746","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"peptide-alanine-alpha-N-acetyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:RXN-17860"],"synonyms":[{"name":"acetyl-CoA:ribosomal-protein-L-alanine N-acetyltransferase activity","type":"related"},{"name":"ribosomal protein S18 acetyltransferase activity","type":"related"},{"name":"ribosomal-protein-alanine N-acetyltransferase activity","type":"broad"}],"termid":"GO:0008999","terms_by_termid":{"GO:0008999":null}}


id: PBO:0039276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG1 like 5, pseudogene","termid":"PBO:0039276"}


id: PBO:0070311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, Ro60-associated Y3","termid":"PBO:0070311"}


id: MONDO:0008795
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aniridia-cerebellar ataxia-intellectual disability syndrome, also known as Gillespie syndrome, is a rare, congenital, neurological disorder characterized by the association of partial bilateral aniridia with non-progressive cerebellar ataxia, and intellectual disability.","definition_xrefs":["Orphanet:1065"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"iridogoniodysgenesis","termid":"MONDO:0011119"}],"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":"aniridia-cerebellar ataxia-intellectual disability syndrome","secondary_identifiers":["SCTID:253176002","GARD:13","UMLS:C0431401","MESH:C536370","OMIM:206700","NORD:786","MEDGEN:96563","ICD9:759.89","DOID:0111578"],"synonyms":[{"name":"Aniridia Cerebellar Ataxia Mental Deficiency","type":"exact"},{"name":"GILLESPIE syndrome","type":"exact"},{"name":"GLSP","type":"exact"},{"name":"Gillespie syndrome","type":"exact"},{"name":"aniridia, cerebellar ataxia and mental deficiency","type":"exact"},{"name":"aniridia, cerebellar ataxia, and intellectual disability","type":"exact"},{"name":"aniridia, cerebellar ataxia, and mental retardation","type":"exact"}],"termid":"MONDO:0008795","xrefs":{"Monarch":{"xref_id":"0008795"}}}


id: PBO:0084711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane half-type ABC transporter; mediates export of peptides generated upon proteolysis of mitochondrial proteins; plays a role in the regulation of cellular resistance to oxidative stress","termid":"PBO:0084711"}


id: PBO:0074964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 114-6","termid":"PBO:0074964"}


id: PR:O14208
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- bit2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14208"],"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 C6B12.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6B12.03c","synonyms":[{"name":"Spom972h-bit2","type":"exact"}],"termid":"PR:O14208"}


id: PBO:0058488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5682","termid":"PBO:0058488"}


id: MONDO:0006712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hazy, swollen cornea.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corneal disorder","termid":"MONDO:0000942"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"corneal edema","secondary_identifiers":["SCTID:27194006","EFO:1000879","ICD9:371.2","ICD9:371.20","MedDRA:10011007","UMLS:C0010037","DOID:11030","MESH:D015715","MEDGEN:3242"],"synonyms":[{"name":"corneal edema","type":"exact"}],"termid":"MONDO:0006712","xrefs":{"Monarch":{"xref_id":"0006712"}}}


id: PBO:0001950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal-ubiquitin fusion protein Ubi3 (predicted)","termid":"PBO:0001950"}


id: MONDO:0859577
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"LADD syndrome","termid":"MONDO:0007872"}],"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":"lacrimoauriculodentodigital syndrome 2","secondary_identifiers":["MEDGEN:1824059","OMIM:620192","DOID:0081371","UMLS:C5774286"],"termid":"MONDO:0859577","xrefs":{"Monarch":{"xref_id":"0859577"}}}


id: GO:0018744
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: limonene-1,2-epoxide + H2O = limonene-1,2-diol. Other substrates include alicyclic and 1-methyl-substituted epoxides, such as 1-methylcyclohexene oxide, indene oxide and cyclohexene oxide.","definition_xrefs":["EC:3.3.2.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epoxide hydrolase activity","termid":"GO:0004301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"limonene-1,2-epoxide hydrolase activity","secondary_identifiers":["UM-BBD_reactionID:r0734","RHEA:10700","MetaCyc:3.3.2.8-RXN"],"synonyms":[{"name":"limonene oxide hydrolase activity","type":"related"}],"termid":"GO:0018744"}


id: PBO:0049838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HEAT repeat containing 1","termid":"PBO:0049838"}


id: PATO:0001559
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A functionality quality which is held by the bearer when the latter is able to perform additional or different function(s).","definition_xrefs":["PATO:MAH"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"functionality","termid":"PATO:0001509"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"having extra function","synonyms":[{"name":"having supernumerary functions","type":"exact"}],"termid":"PATO:0001559"}


id: PBO:0091477
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"I:g.3460318_3460319insC","termid":"PBO:0091477"}


id: GO:0007280
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a pole cell (germline progenitors in insects) from its site of production at the posterior pole of the embryo through to the site where the gonads will form.","definition_xrefs":["GOC:bf","PMID:9988212"],"gene_count":0,"genotype_count":0,"name":"obsolete pole cell migration (obsolete GO:0007280)","termid":"GO:0007280"}


id: GO:1901973
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to proline.","definition_xrefs":["PMID:7730362","GOC:TermGenie","GOC:pm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid binding","termid":"GO:0016597"},{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"organic cyclic compound binding","termid":"GO:0097159"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"}],"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":"proline binding","termid":"GO:1901973"}


id: PBO:0039363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anti-Mullerian hormone","termid":"PBO:0039363"}


id: PBO:0087611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the COMPASS (Set1C) histone H3K4 methyltransferase complex; required for Set1C stability and optimal activity; COMPASS methylates histone H3 on lys 4 and is involved in telomeric silencing; subunit of CPF (cleavage and polyadenylation factor), a complex involved in RNAP II transcription termination","termid":"PBO:0087611"}


id: GO:0071162
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the GINS complex, Cdc45p, and the heterohexameric MCM complex, and that is involved in unwinding DNA during replication.","definition_xrefs":["PMID:19228417","GOC:rb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA replication preinitiation complex","termid":"GO:0031261"},{"relation_name":"part_of","term_name":"nuclear chromosome","termid":"GO:0000228"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005654","GO:0005694","GO:0005634","GO:0032991"],"is_obsolete":false,"name":"CMG complex","synonyms":[{"name":"unwindosome","type":"exact"}],"termid":"GO:0071162"}


id: MONDO:0013271
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"frontonasal dysplasia","termid":"MONDO:0016643"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome","secondary_identifiers":["DOID:0081047","Orphanet:306542","GARD:12640","OMIM:613456","MEDGEN:462056","UMLS:C3150706"],"synonyms":[{"name":"ALX1-related frontonasal dysplasia","type":"exact"},{"name":"FND3","type":"related"},{"name":"frontonasal dysplasia 3","type":"related"},{"name":"frontonasal dysplasia type 3","type":"exact"}],"termid":"MONDO:0013271","xrefs":{"Monarch":{"xref_id":"0013271"}}}


id: PBO:0084077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-binding protein of the rho subfamily of Ras-like proteins; involved in establishment of cell polarity; regulates protein kinase C (Pkc1p) and the cell wall synthesizing enzyme 1,3-beta-glucan synthase (Fks1p and Gsc2p)","termid":"PBO:0084077"}


id: FYPO:0002358
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 dimethylation of lysine at position 9 of histone H3 in silent mating-type cassettes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H3-K9 methylation at silent mating-type cassette during vegetative growth","termid":"FYPO:0005865"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001312","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal histone H3-K9 dimethylation at silent mating-type cassette during vegetative growth","synonyms":[{"name":"normal histone H3-K9 dimethylation at mating-type region heterochromatin during vegetative growth","type":"exact"},{"name":"normal histone H3-K9 dimethylation at silent mating-type cassette during mitotic cell cycle","type":"related"},{"name":"normal histone H3K9me2 at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"normal silent mating-type cassette histone H3-K9 dimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002358"}


id: PBO:0029256
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_chromatin_during_mitotic_S_phase","termid":"PBO:0029256"}


id: GO:0032798
data:
  {"annotated_genes":["SJAG_03221","SJAG_01708"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[106815,109441],"is_not":false,"summary":null,"term":"GO:0032798"}]},"cv_name":"cellular_component","definition":"A conserved DNA recombinase mediator complex that contains two Swi5 monomers and one Sfr1 monomer in Schizosaccharomyces, or orthologs thereof (e.g. Sae3p and Mei5p in Saccharomyces).","definition_xrefs":["PMID:15620352","PMID:16921379"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA recombinase mediator complex","termid":"GO:0033061"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear chromosome","termid":"GO:0000228"},{"relation_name":"part_of","term_name":"chromatin","termid":"GO:0000785"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01708":null,"SJAG_03221":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"Swi5-Sfr1 complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Sae3-Mei5 complex","type":"exact"},{"name":"Swi5 complex","type":"broad"}],"termid":"GO:0032798","terms_by_termid":{"GO:0032798":null}}


id: GO:0042063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in the generation of glial cells. This includes the production of glial progenitors and their differentiation into mature glia.","definition_xrefs":["GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurogenesis","termid":"GO:0022008"}],"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":"gliogenesis","synonyms":[{"name":"glial cell generation","type":"exact"}],"termid":"GO:0042063"}


id: PBO:0087450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of a complex that associates with actin filaments; forms a complex with Tda2p that inhibits barbed end F-actin assembly; elevates actin monomer pools to increase endocytotic efficiency and to regulate the distribution of actin between cables and patches; Aim21p/Tda2p forms a larger complex with actin capping proteins Cap1p and Cap2p; involved in mitochondrial migration along actin filaments; recruited to cortical actin patches by SH3 domain-containing proteins Bbc1p and Abp1p","termid":"PBO:0087450"}


id: GO:0045857
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any heritable epigenetic process that stops, prevents, or reduces the frequency, rate or extent of protein function by self-perpetuating conformational conversions of normal proteins in healthy cells. This is distinct from, though mechanistically analogous to, disease states associated with prion propagation and amyloidogenesis. A single protein, if it carries a glutamine/asparagine-rich ('prion') domain, can sometimes stably exist in at least two distinct physical states, each associated with a different phenotype; propagation of one of these traits is achieved by a self-perpetuating change in the protein from one form to the other, mediated by conformational changes in the glutamine/asparagine-rich domain. Prion domains are both modular and transferable to other proteins, on which they can confer a heritable epigenetic alteration of function; existing bioinformatics data indicate that they are rare in non-eukarya, but common in eukarya.","definition_xrefs":["GOC:go_curators","GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of molecular function, epigenetic (obsolete GO:0045857)","synonyms":[{"name":"down regulation of protein activity, epigenetic","type":"exact"},{"name":"down-regulation of protein activity, epigenetic","type":"exact"},{"name":"downregulation of protein activity, epigenetic","type":"exact"},{"name":"inhibition of protein activity, epigenetic","type":"narrow"},{"name":"negative regulation of protein activity, epigenetic","type":"exact"}],"termid":"GO:0045857"}


id: GO:0016191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of the protein coat on a synaptic vesicle following the pinching step at the end of budding from the presynaptic membrane.","definition_xrefs":["PMID:10099709","GOC:curators","PMID:24596248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin coat disassembly","termid":"GO:0072318"},{"relation_name":"part_of","term_name":"synaptic vesicle endocytosis","termid":"GO:0048488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"synaptic vesicle uncoating","synonyms":[{"name":"synaptic vesicle coat depolymerization","type":"exact"},{"name":"synaptic vesicle coat protein depolymerization","type":"exact"}],"termid":"GO:0016191"}


id: MONDO:0005564
data:
  {"annotated_genes":["SJAG_03689","SJAG_05313","SJAG_00579","SJAG_04213","SJAG_01111","SJAG_04755"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007959"},{"annotations":[85576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011014"},{"annotations":[84411,84412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012252"},{"annotations":[86551,86550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013224"}]},"cv_name":"mondo","definition":"A usually malignant neoplasm composed of primitive (immature) tissues that resemble fetal tissues. Medulloblastoma, Ependymoblastoma, Pineoblastoma, and Wilms tumor are representative embryonal neoplasms. --2003","definition_xrefs":["NCIT:C3264"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00579":null,"SJAG_01111":null,"SJAG_03689":null,"SJAG_04213":null,"SJAG_04755":null,"SJAG_05313":null},"genotype_count":0,"is_obsolete":false,"name":"embryonal neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0027654","DOID:688","EFO:0005784","MEDGEN:45034","MESH:D009373","ONCOTREE:EMBT"],"synonyms":[{"name":"EMBT","type":"related"},{"name":"embryo neoplasm","type":"exact"},{"name":"embryonal cancer","type":"related"},{"name":"embryonal neoplasm","type":"exact"},{"name":"embryonal tumor","type":"exact"},{"name":"embryonal tumour","type":"exact"}],"termid":"MONDO:0005564","terms_by_termid":{"MONDO:0007959":null,"MONDO:0011014":null,"MONDO:0012252":null,"MONDO:0013224":null},"xrefs":{"Monarch":{"xref_id":"0005564"}}}


id: MONDO:0008040
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A myeloid proliferation occurring in newborns with Down syndrome. It is clinically and morphologically indistinguishable from acute myeloid leukemia and is associated with GATA1 mutations. The blasts display morphologic and immunophenotypic features of megakaryocytic lineage. In the majority of patients the myeloid proliferation undergoes spontaneous remission.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloproliferative neoplasm","termid":"MONDO:0020076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"transient myeloproliferative syndrome","secondary_identifiers":["NCIT:C82339","ICDO:9898/1","GARD:12765","ONCOTREE:TAM","OMIM:159595","MESH:C563551","MEDGEN:331782","Orphanet:420611","UMLS:C1834582","HP:0005534","SCTID:721307000","DOID:0060888"],"synonyms":[{"name":"MST","type":"exact"},{"name":"Mst","type":"related"},{"name":"TAM","type":"exact"},{"name":"TMD","type":"exact"},{"name":"Transient abnormal myelopoiesis associated with Down syndrome","type":"exact"},{"name":"leukemia, transient","type":"related"},{"name":"leukemia, transient, of Down syndrome","type":"exact"},{"name":"myeloproliferative syndrome, transient","type":"related"},{"name":"transient abnormal myelopoiesis","type":"exact"},{"name":"transient leukaemia","type":"exact"},{"name":"transient leukemia","type":"exact"},{"name":"transient leurkemia of Down syndrome","type":"exact"},{"name":"transient myeloproliferative disease","type":"exact"},{"name":"transient myeloproliferative disorder","type":"exact"},{"name":"transient myeloproliferative syndrome","type":"exact"},{"name":"transient myeloproliferative syndrome (disease)","type":"exact"}],"termid":"MONDO:0008040","xrefs":{"Monarch":{"xref_id":"0008040"}}}


id: PBO:0072996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scm polycomb group protein like 4","termid":"PBO:0072996"}


id: PBO:0065087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase AMP-activated non-catalytic subunit beta 2","termid":"PBO:0065087"}


id: PBO:0062273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily H member 4 pseudogene","termid":"PBO:0062273"}


id: FYPO:0005938
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 late replication origins is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:24656819","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin at replication origin","termid":"FYPO:0004962"}],"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:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to chromatin at late replication origin","synonyms":[{"name":"normal protein localisation to chromatin at late replication origin","type":"exact"},{"name":"normal protein localization to chromatin at late origin","type":"exact"},{"name":"normal protein localization to chromatin at late replication origin during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at late replication origin during vegetative growth","type":"exact"}],"termid":"FYPO:0005938"}


id: PBO:0083922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Formylkynurenine formamidase; involved in the de novo biosynthesis of NAD from tryptophan via kynurenine","termid":"PBO:0083922"}


id: PBO:0031110
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_regulation_of_translation_in_response_to_stress","termid":"PBO:0031110"}


id: MONDO:0017846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant form of spastic ataxia.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"spastic ataxia","termid":"MONDO:0017845"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant spastic ataxia","secondary_identifiers":["UMLS:C5679899","GARD:21402","ICD10CM:G11.4","icd11.foundation:1327229348","Orphanet:316235","MEDGEN:1842682"],"synonyms":[{"name":"AD-SPAX","type":"exact"},{"name":"spastic ataxia, autosomal dominant","type":"exact"}],"termid":"MONDO:0017846","xrefs":{"Monarch":{"xref_id":"0017846"}}}


id: PBO:0072106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S13 pseudogene 4","termid":"PBO:0072106"}


id: PBO:0049510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 17","termid":"PBO:0049510"}


id: FYPO:0005331
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 repair of pyrimidine-pyrimidone 6-4 photoproducts by error-prone translesion synthesis occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah","PMID:20453833"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal error-prone translesion synthesis","termid":"FYPO:0003892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000298","FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased error-prone translesion synthesis of pyrimidine-pyrimidone 6-4 photoproducts","synonyms":[{"name":"decreased error-prone translesion synthesis across TT-(6-4)","type":"exact"},{"name":"decreased error-prone translesion synthesis of pyrimidine-pyrimidone 6-4 photoproducts during mitotic cell cycle","type":"related"},{"name":"decreased error-prone translesion synthesis of pyrimidine-pyrimidone 6-4 photoproducts during vegetative growth","type":"exact"}],"termid":"FYPO:0005331"}


id: MONDO:0005007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive adenocarcinoma of the colon characterized by the presence of pools of extracellular mucin. Malignant glandular epithelial cells are present in the mucin collections. Mucin constitutes more than 50% of the lesion.","definition_xrefs":["NCIT:C7966"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon adenocarcinoma","termid":"MONDO:0002271"},{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"colon mucinous adenocarcinoma","secondary_identifiers":["DOID:3029","MEDGEN:76007","EFO:0000364","UMLS:C0279639"],"synonyms":[{"name":"colloid adenocarcinoma of colon","type":"exact"},{"name":"colloid adenocarcinoma of the colon","type":"exact"},{"name":"colloid colon adenocarcinoma","type":"exact"},{"name":"colloidal adenocarcinoma of colon","type":"exact"},{"name":"colloidal adenocarcinoma of the colon","type":"exact"},{"name":"colloidal colon adenocarcinoma","type":"exact"},{"name":"colon colloid adenocarcinoma","type":"exact"},{"name":"colon colloidal adenocarcinoma","type":"exact"},{"name":"colon mucinous adenocarcinoma","type":"exact"},{"name":"colonic colloid adenocarcinoma","type":"exact"},{"name":"colonic colloidal adenocarcinoma","type":"exact"},{"name":"colonic mucinous adenocarcinoma","type":"exact"},{"name":"mucinous adenocarcinoma of colon","type":"exact"},{"name":"mucinous adenocarcinoma of the colon","type":"exact"},{"name":"mucinous colon adenocarcinoma","type":"exact"}],"termid":"MONDO:0005007","xrefs":{"Monarch":{"xref_id":"0005007"}}}


id: GO:0061823
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ring-like structure observed at the base of the ciliary cap of insect spermatids. This structure may anchor the axoneme to the ciliary cap membrane and/or act as a diffusion barrier, proposed to be analogous to the annulus of mammalian sperm flagellum.","definition_xrefs":["PMID:4903810","PMID:25447994"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cilium","termid":"GO:0005929"}],"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":"ring centriole","termid":"GO:0061823"}


id: PR:P05734
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl1901 gene.","definition_xrefs":["UniProtKB:P05734","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":"60S ribosomal protein L19-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC56F2.02","synonyms":[{"name":"Spom972h-rpl1901","type":"exact"},{"name":"YL15 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P05734"}


id: PBO:0052413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2","termid":"PBO:0052413"}


id: PBO:0062949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasomal ATPase associated factor 1","termid":"PBO:0062949"}


id: MONDO:0054561
data:
  {"annotated_genes":["SJAG_04582"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86110],"is_not":false,"summary":null,"term":"MONDO:0054561"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"anauxetic dysplasia","termid":"MONDO:0011773"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04582":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"anauxetic dysplasia 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080962","OMIM:617396","UMLS:C4479357","MEDGEN:1384439"],"synonyms":[{"name":"ANXD2","type":"related"},{"name":"anauxetic dysplasia 2","type":"exact"}],"termid":"MONDO:0054561","terms_by_termid":{"MONDO:0054561":null},"xrefs":{"Monarch":{"xref_id":"0054561"}}}


id: GO:0044847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which a symbiont acquires iron from its host, either from heme or other iron containing molecules such as transferrin and lactoferrin. Begins with either the secretion of symbiont gene products that bind iron- or heme-containing molecules (siderophores and hemophores) from the symbiont cell into the host, or by expression of receptors that bind iron- or heme-containing molecules on the symbiont cell surface. Ends when the iron-containing compound is transported into the symbiont cell.","definition_xrefs":["PMID:15487950","PMID:22865843"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquisition of nutrients from host","termid":"GO:0044002"}],"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":"iron acquisition from host","secondary_identifiers":["GO:0052099"],"synonyms":[{"name":"acquisition by organism of nutrients from host via siderophores","type":"related"},{"name":"acquisition by symbiont of nutrients from host via siderophores","type":"narrow"},{"name":"heme acquisition","type":"related"},{"name":"iron acquisition","type":"broad"},{"name":"iron acquisition by symbiont from host","type":"exact"},{"name":"iron acquisition by symbiont from host heme","type":"narrow"}],"termid":"GO:0044847"}


id: MONDO:0003702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign neoplasm characterized by the presence of smooth muscle cells growing within the veins of the uterine corpus. The intravascular neoplasm growth occurs outside the confines of an adjacent leiomyoma.","definition_xrefs":["NCIT:C5356"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"uterine corpus diffuse leiomyomatosis","termid":"MONDO:0003704"},{"relation_name":"is_a","term_name":"uterine benign neoplasm","termid":"MONDO:0000632"},{"relation_name":"is_a","term_name":"intravenous leiomyomatosis","termid":"MONDO:0003614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterus intravascular leiomyomatosis","secondary_identifiers":["DOID:5915"],"synonyms":[{"name":"intravascular leiomyomatosis of the uterus","type":"exact"},{"name":"intravascular leiomyomatosis of uterus","type":"exact"},{"name":"intravenous leiomyomatosis of the uterus","type":"exact"},{"name":"intravenous leiomyomatosis of uterus","type":"exact"},{"name":"uterine corpus intravenous leiomyomatosis","type":"exact"},{"name":"uterus intravenous leiomyomatosis","type":"exact"}],"termid":"MONDO:0003702","xrefs":{"Monarch":{"xref_id":"0003702"}}}


id: MONDO:0100533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing intracerebral hemorrhage.","definition_xrefs":["MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemorrhage, intracerebral, susceptibility to","secondary_identifiers":["MEDGEN:482735","OMIM:614519","UMLS:C3281105"],"synonyms":[{"name":"ICH","type":"exact"}],"termid":"MONDO:0100533","xrefs":{"Monarch":{"xref_id":"0100533"}}}


id: GO:0045443
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of juvenile hormones, the three sesquiterpenoid derivatives that function to maintain the larval state of insects at molting and that may be required for other processes, e.g. oogenesis.","definition_xrefs":["GOC:go_curators","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpenoid transport","termid":"GO:0046865"},{"relation_name":"is_a","term_name":"endocrine hormone secretion","termid":"GO:0060986"},{"relation_name":"is_a","term_name":"lipid export from cell","termid":"GO:0140353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"juvenile hormone secretion","termid":"GO:0045443"}


id: MONDO:0043862
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pathologic process in the larynx that affects the production of speech. Causes include vocal cord paresis, vocal cord nodule, vocal cord polyp, and laryngitis.","definition_xrefs":["NCIT:C3441"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laryngeal disorder","termid":"MONDO:0004382"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"voice disorders","secondary_identifiers":["MEDGEN:12120","UMLS:C0042940","SCTID:71941009","EFO:0009692","MESH:D014832"],"synonyms":[{"name":"neurologic dysphonia","type":"related"},{"name":"neurologic voice disorder","type":"exact"},{"name":"voice disorder","type":"exact"}],"termid":"MONDO:0043862","xrefs":{"Monarch":{"xref_id":"0043862"}}}


id: PBO:0091650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane inorganic phosphate transmembrane transporter Pho841","termid":"PBO:0091650"}


id: MONDO:0014385
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any amelogenesis imperfecta in which the cause of the disease is a mutation in the SLC24A4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amelogenesis imperfecta type 2","termid":"MONDO:0015048"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amelogenesis imperfecta hypomaturation type 2A5","secondary_identifiers":["DOID:0110063","GARD:16028","MEDGEN:863015","UMLS:C4014578","OMIM:615887"],"synonyms":[{"name":"AI2A5","type":"exact"},{"name":"SLC24A4 amelogenesis imperfecta","type":"exact"},{"name":"amelogenesis imperfecta caused by mutation in SLC24A4","type":"exact"},{"name":"amelogenesis imperfecta hypomaturation type IIA5","type":"exact"},{"name":"amelogenesis imperfecta type IIA5","type":"exact"},{"name":"amelogenesis imperfecta, hypomaturation type, IIA5","type":"related"},{"name":"amelogenesis imperfecta, type IIA5","type":"exact"}],"termid":"MONDO:0014385","xrefs":{"Monarch":{"xref_id":"0014385"}}}


id: PR:G2TRS2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- new20 gene.","definition_xrefs":["UniProtKB:G2TRS2","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 new20 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC839.19","synonyms":[{"name":"Spom972h-new20","type":"exact"}],"termid":"PR:G2TRS2"}


id: PBO:0052782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 19 pseudogene 6","termid":"PBO:0052782"}


id: PBO:0114949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-CHY type zinc finger protein involved in rescue of stalled ribosomes","termid":"PBO:0114949"}


id: PBO:0078871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transient receptor potential cation channel subfamily M member 5","termid":"PBO:0078871"}


id: PBO:0000358
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5.4.2.3","termid":"PBO:0000358"}


id: MONDO:0002460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the lacrimal apparatus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"ocular cancer","termid":"MONDO:0002236"},{"relation_name":"is_a","term_name":"lacrimal apparatus disorder","termid":"MONDO:0001854"},{"relation_name":"is_a","term_name":"ocular cancer","termid":"MONDO:0002236"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004992"],"is_obsolete":false,"name":"lacrimal system cancer","secondary_identifiers":["NCIT:C5102","UMLS:C1334361","MEDGEN:272790","SCTID:416510003","DOID:292"],"synonyms":[{"name":"cancer of lacrimal apparatus","type":"exact"},{"name":"lacrimal apparatus cancer","type":"exact"},{"name":"lacrimal system neoplasm","type":"exact"},{"name":"lacrimal system neoplasms","type":"exact"},{"name":"lacrimal system tumor","type":"exact"},{"name":"lacrimal system tumour","type":"exact"},{"name":"malignant lacrimal apparatus neoplasm","type":"exact"},{"name":"malignant neoplasm of lacrimal apparatus","type":"exact"},{"name":"neoplasm of lacrimal system","type":"exact"},{"name":"neoplasm of the lacrimal system","type":"exact"},{"name":"tumor of lacrimal system","type":"exact"},{"name":"tumor of the lacrimal system","type":"exact"},{"name":"tumour of lacrimal system","type":"exact"},{"name":"tumour of the lacrimal system","type":"exact"}],"termid":"MONDO:0002460","xrefs":{"Monarch":{"xref_id":"0002460"}}}


id: PBO:0028064
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_plasma_membrane_of_cell_tip_during_vegetative_growth","termid":"PBO:0028064"}


id: GO:0075041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of turgor formation in the symbiont appressorium.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of establishment of turgor in appressorium (obsolete GO:0075041)","termid":"GO:0075041"}


id: PBO:0040422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V0 subunit d2","termid":"PBO:0040422"}


id: GO:0050131
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an N-methyl-L-amino acid + H2O + O2 = an L-amino acid + formaldehyde + H2O2.","definition_xrefs":["EC:1.5.3.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor","termid":"GO:0016647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"N-methyl-L-amino-acid oxidase activity","secondary_identifiers":["MetaCyc:N-METHYL-L-AMINO-ACID-OXIDASE-RXN","RHEA:11472"],"synonyms":[{"name":"N-methyl-L-amino-acid:oxygen oxidoreductase (demethylating)","type":"related"},{"name":"N-methylamino acid oxidase activity","type":"related"}],"termid":"GO:0050131"}


id: MONDO:0012351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndactyly type 1","termid":"MONDO:0008512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zygodactyly type 1","secondary_identifiers":["UMLS:C1853294","GARD:17357","DOID:0111820","OMIM:609815","MESH:C565223","MEDGEN:377870","Orphanet:295187","icd11.foundation:1671375617"],"synonyms":[{"name":"SD1, Weidenreich type","type":"exact"},{"name":"SD1a","type":"exact"},{"name":"ZYGODACTYLY 1","type":"related"},{"name":"Zd1","type":"related"},{"name":"Zygodactyly, Weidenreich type","type":"exact"},{"name":"syndactyly type 1, Weidenreich type","type":"exact"},{"name":"syndactyly type 1a","type":"exact"},{"name":"zygodactyly type 1","type":"exact"}],"termid":"MONDO:0012351","xrefs":{"Monarch":{"xref_id":"0012351"}}}


id: PBO:0036452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin Aly1 related Aly2","termid":"PBO:0036452"}


id: PBO:0061221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein 12","termid":"PBO:0061221"}


id: PBO:0063398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"programmed cell death 10","termid":"PBO:0063398"}


id: PBO:0038626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atypical chemokine receptor 2","termid":"PBO:0038626"}


id: GO:0061122
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of directed movement of a motile cell or organism up a concentration gradient of 3',5'-cAMP.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of positive chemotaxis","termid":"GO:0050927"},{"relation_name":"is_a","term_name":"regulation of positive chemotaxis to cAMP","termid":"GO:0061118"},{"relation_name":"positively_regulates","term_name":"chemotaxis to cAMP","termid":"GO:0043327"}],"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 positive chemotaxis to cAMP","termid":"GO:0061122"}


id: PBO:0002145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPR repeat protein, SGT2 family (predicted)","termid":"PBO:0002145"}


id: PBO:0017645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choline/ethanolamine kinase Eki1 (predicted)","termid":"PBO:0017645"}


id: MOD:01694
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct between an L-cysteine residue and the bioluminescent compound didehydrocoelenterazine to form S-(coelenterazin-3a-yl)-L-cysteine.","definition_xrefs":["RESID:AA0526","ChEBI:2311","PubMed:18997450"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-(coelenterazin-3a-yl)-L-cysteine","synonyms":[{"name":"(2R)-2-amino-3-([(4-hydroxyphenyl)(8-benzyl-3-oxo-6-[4-hydroxyphenyl]-3,7-dihydroimidazo[1,2-a]pyrazin-2-yl)methyl]sulfanyl)propanoic acid","type":"exact"},{"name":"MOD_RES S-(coelenterazin-3a-yl)cysteine","type":"exact"},{"name":"S-(coelenterazin-3a-yl)-L-cysteine","type":"exact"},{"name":"dehydrocoelenterazine cysteine adduct","type":"exact"},{"name":"symplectin chromophore","type":"exact"}],"termid":"MOD:01694"}


id: GO:0042287
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a major histocompatibility complex molecule; a set of molecules displayed on cell surfaces that are responsible for lymphocyte recognition and antigen presentation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"MHC protein binding","synonyms":[{"name":"major histocompatibility complex binding","type":"exact"},{"name":"major histocompatibility complex ligand","type":"narrow"}],"termid":"GO:0042287"}


id: MONDO:0014816
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"split-foot malformation-mesoaxial polydactyly syndrome","secondary_identifiers":["UMLS:C5567487","GARD:17889","MEDGEN:1798910","OMIM:616890","Orphanet:488232"],"synonyms":[{"name":"SFMMP","type":"exact"},{"name":"split-foot malformation with mesoaxial polydactyly","type":"exact"},{"name":"split-foot malformation-mesoaxial polydactyly-nail abnormalities-sensorineural hearing loss syndrome","type":"exact"}],"termid":"MONDO:0014816","xrefs":{"Monarch":{"xref_id":"0014816"}}}


id: PBO:0042321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD40 ligand","termid":"PBO:0042321"}


id: GO:0047414
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2Z)-2-(acetamidomethylene)-3-(hydroxymethyl)succinate + 2 H2O + H+ = 2-(hydroxymethyl)-4-oxobutanoate + acetate + CO2 + NH4.","definition_xrefs":["RHEA:17677","EC:3.5.1.66"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016810"],"is_obsolete":false,"name":"2-(hydroxymethyl)-3-(acetamidomethylene)succinate hydrolase activity","secondary_identifiers":["KEGG_REACTION:R04397","MetaCyc:3.5.1.66-RXN","Wikipedia:2-(hydroxymethyl)-3-(acetamidomethylene)succinate_amidohydrolase_(deaminating\\,_decarboxylating)"],"synonyms":[{"name":"2-(hydroxymethyl)-3-(acetamidomethylene)succinate amidohydrolase (deaminating, decarboxylating)","type":"related"},{"name":"alpha-hydroxymethyl-alpha'-(N-acetylaminomethylene)succinic acid hydrolase activity","type":"related"},{"name":"compound B hydrolase activity","type":"related"}],"termid":"GO:0047414"}


id: PBO:0027470
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_NAD(P)H_oxidase_activity","termid":"PBO:0027470"}


id: GO:0097030
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a centromere-specific nucleosome, a form of nucleosome located only at the centromere, in which the histone H3 is replaced by the variant form CENP-A (sometimes known as CenH3).","definition_xrefs":["GOC:jp","PMID:21412236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleosome binding","termid":"GO:0031491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"CENP-A containing nucleosome binding","synonyms":[{"name":"centromere-specific nucleosome binding","type":"related"},{"name":"centromeric nucleosome binding","type":"related"}],"termid":"GO:0097030"}


id: MONDO:0006365
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hamartomatous polyp that occurs in the stomach, small and large intestines, and rarely within the esophagus, nasopharynx and the urinary tract. The Peutz-Jeghers polyps are grossly lobulated and dark. Microscopically, they have a central core of smooth muscle covered by mucosa. The smooth muscle shows tree-like branching. The question of whether or not the Peutz-Jeghers polyp is precancerous is a matter of controversy. The loss of heterozygosity on chromosome 19p (where the responsible gene LKB1 is located) suggests that the increased risk of malignancy may be due to malignant transformation from hamartoma to adenocarcinoma. --2002","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastrointestinal hamartoma","termid":"MONDO:0006231"}],"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":"Peutz-Jeghers polyp","secondary_identifiers":["EFO:1000470","NCIT:C4733","UMLS:C0456487","MEDGEN:141582"],"synonyms":[{"name":"Peutz Jeghers polyp","type":"exact"},{"name":"Peutz-Jeghers polyp","type":"exact"}],"termid":"MONDO:0006365","xrefs":{"Monarch":{"xref_id":"0006365"}}}


id: MONDO:0007462
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple sclerosis, susceptibility to","secondary_identifiers":["MEDGEN:358269","OMIMPS:126200","UMLS:C1868685"],"synonyms":[{"name":"MS","type":"related"},{"name":"disseminated sclerosis","type":"related"}],"termid":"MONDO:0007462","xrefs":{"Monarch":{"xref_id":"0007462"}}}


id: PBO:0056454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methionyl-tRNA synthetase 2, mitochondrial","termid":"PBO:0056454"}


id: MONDO:0019333
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hyperinsulinemic hypoglycemia, familial, 1","termid":"MONDO:0009734"},{"relation_name":"is_a","term_name":"diazoxide-resistant diffuse hyperinsulinism","termid":"MONDO:0015625"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0004335"],"is_obsolete":false,"name":"autosomal recessive hyperinsulinism due to SUR1 deficiency","secondary_identifiers":["Orphanet:79643","MEDGEN:1683144","UMLS:C5191077","GARD:16726"],"synonyms":[{"name":"autosomal recessive hyperinsulinemic hypoglycemia due to SUR1 deficiency","type":"exact"}],"termid":"MONDO:0019333","xrefs":{"Monarch":{"xref_id":"0019333"}}}


id: PBO:0005309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U4/U6 x U5 tri-snRNP complex subunit Dim1","termid":"PBO:0005309"}


id: MONDO:0971011
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"MHC class I deficiency","termid":"MONDO:0011476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"MHC class I deficiency 2","secondary_identifiers":["OMIM:620813"],"termid":"MONDO:0971011","xrefs":{"Monarch":{"xref_id":"0971011"}}}


id: GO:0016071
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id: GO:0007565
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id: MONDO:0014313
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id: PBO:0061710
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id: GO:1901167
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id: PBO:0045144
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id: PBO:0089000
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id: PBO:0082457
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id: FYPO:0001399
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id: GO:0015165
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id: GO:0004291
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id: MONDO:0000324
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id: PBO:0039234
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id: PBO:0050842
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id: MONDO:0011644
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id: MONDO:0015748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"White sponge nevus (WSN) is a rare and autosomal dominant genetic disease in which the oral mucosa is white or grayish, thickened, folded, and spongy. The onset is early in life, and both sexes are affected equally. Other common sites include the tongue, floor of the mouth, and alveolar mucosa.","definition_xrefs":["Orphanet:171723"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"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":"hereditary mucosal leukokeratosis","secondary_identifiers":["GARD:8501","DOID:0050448","ICD9:528.6","NCIT:C84760","MEDGEN:328433","MESH:D053529","UMLS:C1721005","OMIMPS:193900","SCTID:389203001"],"synonyms":[{"name":"White sponge nevus of Cannon","type":"exact"},{"name":"hereditary mucosal leukokeratosis","type":"exact"},{"name":"white sponge nevus","type":"exact"},{"name":"white sponge nevus of Cannon","type":"exact"}],"termid":"MONDO:0015748","xrefs":{"Monarch":{"xref_id":"0015748"}}}


id: GO:1900238
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of regulation of metanephric mesenchymal cell migration, by platelet-derived growth factor receptor-beta signaling pathway.","definition_xrefs":["GOC:yaf","GOC:TermGenie","PMID:19019919","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"platelet-derived growth factor receptor-beta signaling pathway","termid":"GO:0035791"},{"relation_name":"is_a","term_name":"regulation of metanephric mesenchymal cell migration","termid":"GO:2000589"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signaling pathway","synonyms":[{"name":"regulation of metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signalling pathway","type":"exact"},{"name":"regulation of metanephric mesenchyme chemotaxis by platelet-derived growth factor receptor-beta signaling pathway","type":"related"}],"termid":"GO:1900238"}


id: GO:0008583
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an undifferentiated cell acquires the features of a mystery cell. The mystery cells are a precluster of cells that emerge from the compound eye morphogenetic furrow, normally positioned between R3 and R4. They then disappear into the surrounding pool of undifferentiated cells and have no known fate in the mature ommatidium. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["ISBN:0632030488","PMID:1295747"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"compound eye morphogenesis","termid":"GO:0001745"}],"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":"mystery cell differentiation","termid":"GO:0008583"}


id: PBO:0044251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CWC25 spliceosome associated protein homolog","termid":"PBO:0044251"}


id: GO:1902459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of stem cell population maintenance.","definition_xrefs":["GOC:TermGenie","PMID:22969033","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of stem cell population maintenance","termid":"GO:2000036"},{"relation_name":"positively_regulates","term_name":"stem cell population maintenance","termid":"GO:0019827"}],"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 stem cell population maintenance","synonyms":[{"name":"activation of maintenance of pluripotency","type":"related"},{"name":"activation of stem cell maintenance","type":"narrow"},{"name":"positive regulation of maintenance of pluripotency","type":"related"},{"name":"up regulation of maintenance of pluripotency","type":"related"},{"name":"up regulation of stem cell maintenance","type":"exact"},{"name":"up-regulation of maintenance of pluripotency","type":"related"},{"name":"up-regulation of stem cell maintenance","type":"exact"},{"name":"upregulation of maintenance of pluripotency","type":"related"},{"name":"upregulation of stem cell maintenance","type":"exact"}],"termid":"GO:1902459"}


id: MONDO:0015407
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cerebrofacial arteriovenous metameric syndrome","termid":"MONDO:0015405"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebrofacial arteriovenous metameric syndrome type 3","secondary_identifiers":["SCTID:703268008","UMLS:C3838691","GARD:19960","icd11.foundation:1048965538","MEDGEN:824537","Orphanet:141199"],"synonyms":[{"name":"CAMS3","type":"exact"}],"termid":"MONDO:0015407","xrefs":{"Monarch":{"xref_id":"0015407"}}}


id: GO:0046257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of 2,4,6-trinitrotoluene, 1-methyl-2,4,6-trinitrobenzene, a highly explosive pale yellow crystalline solid, in the absence of oxygen.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete anaerobic 2,4,6-trinitrotoluene biosynthetic process (obsolete GO:0046257)","synonyms":[{"name":"anaerobic 2,4,6-trinitrotoluene anabolism","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene biosynthesis","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene biosynthetic process","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene formation","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene synthesis","type":"exact"}],"termid":"GO:0046257"}


id: MONDO:0018276
data:
  {"annotated_genes":["SJAG_03188","SJAG_05219","SJAG_04053","SJAG_01491","SJAG_04316","SJAG_00831"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012248"},{"annotations":[85891,85892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"},{"annotations":[85173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014142"},{"annotations":[84515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014023"},{"annotations":[84387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013049"},{"annotations":[85078,85079,85080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009364"},{"annotations":[85166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014140"},{"annotations":[85885,85886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013154"},{"annotations":[84475],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033556"},{"annotations":[85890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013159"},{"annotations":[85171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014141"},{"annotations":[85889,85888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013160"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00831":null,"SJAG_01491":null,"SJAG_03188":null,"SJAG_04053":null,"SJAG_04316":null,"SJAG_05219":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:12584","Orphanet:370953","UMLS:C5679911","DOID:0112374","MEDGEN:1842215"],"synonyms":[{"name":"CMD due to dystroglycanopathy","type":"exact"},{"name":"congenital muscular dystrophy due to dystroglycanopathy","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy","type":"exact"}],"termid":"MONDO:0018276","terms_by_termid":{"MONDO:0009364":null,"MONDO:0012248":null,"MONDO:0013049":null,"MONDO:0013154":null,"MONDO:0013159":null,"MONDO:0013160":null,"MONDO:0013162":null,"MONDO:0014023":null,"MONDO:0014140":null,"MONDO:0014141":null,"MONDO:0014142":null,"MONDO:0033556":null},"xrefs":{"Monarch":{"xref_id":"0018276"}}}


id: GO:0003846
data:
  {"annotated_genes":["SJAG_03609"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[113321],"is_not":false,"summary":null,"term":"GO:0003846"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acyl-CoA + 2-acylglycerol = CoA + diacylglycerol.","definition_xrefs":["RHEA:16741","PMID:4016575"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylglycerol O-acyltransferase activity","termid":"GO:0016411"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03609":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"2-acylglycerol O-acyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:2.3.1.22","MetaCyc:2-ACYLGLYCEROL-O-ACYLTRANSFERASE-RXN","Reactome:R-HSA-5696448","Reactome:R-HSA-6800334"],"synonyms":[{"name":"acyl coenzyme A-monoglyceride acyltransferase activity","type":"related"},{"name":"acyl-CoA:2-acylglycerol O-acyltransferase activity","type":"related"},{"name":"acylglycerol palmitoyltransferase activity","type":"related"},{"name":"monoacylglycerol acyltransferase activity","type":"related"},{"name":"monoglyceride acyltransferase activity","type":"related"}],"termid":"GO:0003846","terms_by_termid":{"GO:0003846":null}}


id: GO:0030329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving prenylcysteine, 3-methyl-2-buten-1-yl-cysteine, a derivative of the amino acid cysteine formed by the covalent addition of a prenyl residue.","definition_xrefs":["GOC:ai","PMID:16627894"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"}],"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":"prenylcysteine metabolic process","synonyms":[{"name":"prenylcysteine metabolism","type":"exact"}],"termid":"GO:0030329"}


id: PATO:0000336
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color quality inhering in a bearer by virtue of the bearer's having color.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color","termid":"PATO:0000014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colored","secondary_identifiers":["PATO:0000332"],"synonyms":[{"name":"pigmented","type":"related"}],"termid":"PATO:0000336"}


id: PBO:0050341
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 43","termid":"PBO:0050341"}


id: PBO:0030471
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_spindle_pole_body_separation","termid":"PBO:0030471"}


id: PBO:0048738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate-ammonia ligase","termid":"PBO:0048738"}


id: PBO:0027712
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_branched,_swollen,_elongated,_multiseptate_vegetative_cell","termid":"PBO:0027712"}


id: GO:0106402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a Lewis x epitope, a trisaccharide (beta-D-galactosyl-(1,4)-[alpha-L-fucosyl-(1,3)]-N-acetyl-beta-D-glucosamine) expressed on several glycolipids, glycoproteins, and proteoglycans of the nervous system. The related Lewis x epitope is formed by alpha(1,3) fucosylation of the N-acetylglucosaminyl residue of a type 2 histo-blood group antigen precursor disaccharide.","definition_xrefs":["PMID:23000574","PMID:16973732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate derivative biosynthetic process","termid":"GO:1901137"}],"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":"Lewis x epitope biosynthetic process","synonyms":[{"name":"sLeX biosynthetic process","type":"related"},{"name":"sialyl-Lewis X biosynthetic process","type":"related"}],"termid":"GO:0106402"}


id: PR:O94703
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerase I subunit RPA12 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11239:SF3","OMA:SCHPO04551","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":"DNA-directed RNA polymerase I subunit RPA12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1259.03","secondary_identifiers":["UniProtKB:O94703"],"synonyms":[{"name":"DNA-directed RNA polymerase I 13.1 kDa polypeptide (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ZNRD1","type":"exact"}],"termid":"PR:O94703"}


id: PBO:0054573
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 1975","termid":"PBO:0054573"}


id: GO:0050128
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-feruloylglycine + H2O = ferulate + glycine.","definition_xrefs":["RHEA:10484","EC:3.5.1.71"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"N-feruloylglycine deacylase activity","secondary_identifiers":["KEGG_REACTION:R03579","MetaCyc:N-FERULOYLGLYCINE-DEACYLASE-RXN"],"synonyms":[{"name":"N-feruloylglycine amidohydrolase activity","type":"related"},{"name":"N-feruloylglycine hydrolase activity","type":"related"}],"termid":"GO:0050128"}


id: PBO:0078312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asp (GTC) 8-1","termid":"PBO:0078312"}


id: PR:Q7Z996
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pop8 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q7Z996"],"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":"ribonucleases P protein subunit pop8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1709.20","synonyms":[{"name":"Spom972h-pop8","type":"exact"}],"termid":"PR:Q7Z996"}


id: GO:0034196
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of an acylglycerol into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. An acylglycerol is any mono-, di- or triester of glycerol with (one or more) fatty acids.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transport","termid":"GO:0006869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"acylglycerol transport","synonyms":[{"name":"glyceride transport","type":"exact"}],"termid":"GO:0034196"}


id: GO:0045182
data:
  {"annotated_genes":["SJAG_03147","SJAG_03629","SJAG_02471","SJAG_01659","SJAG_02353","SJAG_01517","SJAG_03550","SJAG_02601","SJAG_02376","SJAG_01487","SJAG_00308","SJAG_03788","SJAG_05003","SJAG_01249","SJAG_02738","SJAG_02189","SJAG_02180","SJAG_02995","SJAG_01813","SJAG_02164","SJAG_01518","SJAG_05221","SJAG_00466","SJAG_00786","SJAG_01696","SJAG_02390","SJAG_04772","SJAG_00507","SJAG_02628","SJAG_04157","SJAG_04900","SJAG_04744","SJAG_03232","SJAG_00662","SJAG_03472","SJAG_02493","SJAG_04283","SJAG_04891","SJAG_05000","SJAG_05332","SJAG_02812","SJAG_04981","SJAG_01079","SJAG_01438","SJAG_02307","SJAG_02017","SJAG_01117","SJAG_02638","SJAG_02856","SJAG_01954","SJAG_00338","SJAG_02043","SJAG_03461","SJAG_01851","SJAG_01576","SJAG_05271","SJAG_03996","SJAG_03223","SJAG_04635","SJAG_03433","SJAG_03678","SJAG_01643","SJAG_04959","SJAG_03732"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115957],"is_not":false,"summary":null,"term":"GO:0045182"},{"annotations":[118041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000900"},{"annotations":[111805,87782,98648,99647,101098,97905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008494"},{"annotations":[111546,111285,116088,97505,102066,112006,113861,108322,118083,94322,117607,118082,117608,92804,92806,111545,117609,94321,97504,111544,108323,94539,72094,92805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003746"},{"annotations":[104751,95861,89149,96431,101816,95783,96987,97007,96051,96926,91972,93988,106470,99691,103929,104486,104583,109758,113111,110484,99292,114753,97583,104770,86741,95068,102392,89571,103234,89112,109844,104779,98126,106179],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003743"},{"annotations":[116629,90303,95135,106339,97851,101254,115170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003747"},{"annotations":[97852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016150"},{"annotations":[90304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016149"},{"annotations":[111298],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030371"},{"annotations":[94324,103877,94323,108325,108324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008079"}]},"cv_name":"molecular_function","definition":"Any molecular function involved in the initiation, activation, perpetuation, repression or termination of polypeptide synthesis at the ribosome.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":64,"genes_by_uniquename":{"SJAG_00308":null,"SJAG_00338":null,"SJAG_00466":null,"SJAG_00507":null,"SJAG_00662":null,"SJAG_00786":null,"SJAG_01079":null,"SJAG_01117":null,"SJAG_01249":null,"SJAG_01438":null,"SJAG_01487":null,"SJAG_01517":null,"SJAG_01518":null,"SJAG_01576":null,"SJAG_01643":null,"SJAG_01659":null,"SJAG_01696":null,"SJAG_01813":null,"SJAG_01851":null,"SJAG_01954":null,"SJAG_02017":null,"SJAG_02043":null,"SJAG_02164":null,"SJAG_02180":null,"SJAG_02189":null,"SJAG_02307":null,"SJAG_02353":null,"SJAG_02376":null,"SJAG_02390":null,"SJAG_02471":null,"SJAG_02493":null,"SJAG_02601":null,"SJAG_02628":null,"SJAG_02638":null,"SJAG_02738":null,"SJAG_02812":null,"SJAG_02856":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03223":null,"SJAG_03232":null,"SJAG_03433":null,"SJAG_03461":null,"SJAG_03472":null,"SJAG_03550":null,"SJAG_03629":null,"SJAG_03678":null,"SJAG_03732":null,"SJAG_03788":null,"SJAG_03996":null,"SJAG_04157":null,"SJAG_04283":null,"SJAG_04635":null,"SJAG_04744":null,"SJAG_04772":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04959":null,"SJAG_04981":null,"SJAG_05000":null,"SJAG_05003":null,"SJAG_05221":null,"SJAG_05271":null,"SJAG_05332":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"translation regulator activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"translation factor activity","type":"exact"}],"termid":"GO:0045182","terms_by_termid":{"GO:0000900":null,"GO:0003743":null,"GO:0003746":null,"GO:0003747":null,"GO:0008079":null,"GO:0008494":null,"GO:0016149":null,"GO:0016150":null,"GO:0030371":null,"GO:0045182":null}}


id: RO:0002206
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x expressed in y if and only if there is a gene expression process (GO:0010467) that occurs in y, and one of the following holds: (i) x is a gene, and x is transcribed into a transcript as part of the gene expression process (ii) x is a transcript, and the transcription of x is part of the gene expression process (iii) x is a mature gene product such as a protein, and x was translated or otherwise processes from a transcript that was transcribed as part of this gene expression process","direct_ancestors":[{"relation_name":"is_a","term_name":"genomically_related_to","termid":"RO:0002330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed_in","termid":"RO:0002206"}


id: GO:0009337
data:
  {"annotated_genes":["SJAG_05027","SJAG_01693"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[86978,116606],"is_not":false,"summary":null,"term":"GO:0009337"}]},"cv_name":"cellular_component","definition":"A multisubunit iron flavoprotein, which in yeast is composed of 2 alpha and 2 beta subunits. Catalyzes the reduction of sulfite to sulfide.","definition_xrefs":["GOC:jl","PMID:6751400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01693":null,"SJAG_05027":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"sulfite reductase complex (NADPH)","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"sulphite reductase complex (NADPH)","type":"exact"}],"termid":"GO:0009337","terms_by_termid":{"GO:0009337":null}}


id: MONDO:0017837
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may include eye involvement (optic atrophy, diplopia), neuromuscular involvement (ataxia, pyramidal syndrome, gait disturbance) and sensory disorder. There have been no further descriptions in the literature since 1992.","definition_xrefs":["Orphanet:3151"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"},{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"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":"multiple sclerosis-ichthyosis-factor VIII deficiency syndrome","secondary_identifiers":["MEDGEN:1391655","UMLS:C4518551","GARD:18787"],"termid":"MONDO:0017837","xrefs":{"Monarch":{"xref_id":"0017837"}}}


id: GO:0018342
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The covalent attachment of a prenyl group to a protein; geranyl, farnesyl, or geranylgeranyl groups may be added.","definition_xrefs":["GOC:di","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"},{"relation_name":"is_a","term_name":"prenylation","termid":"GO:0097354"}],"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":"protein prenylation","secondary_identifiers":["GO:0018346"],"synonyms":[{"name":"C-terminal protein prenylation","type":"narrow"},{"name":"protein amino acid prenylation","type":"exact"}],"termid":"GO:0018342"}


id: PBO:0004338
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.2.1.51","termid":"PBO:0004338"}


id: MONDO:1011705
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"combined deficiency of factors VIII, IX, and X, non-human animal","secondary_identifiers":["OMIA:001983"],"termid":"MONDO:1011705","xrefs":{"Monarch":{"xref_id":"1011705"}}}


id: PBO:0087801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tail-anchored ER membrane protein of unknown function; substrate of the phosphatase calcineurin; interacts with homolog Frt2p; promotes cell growth in stress conditions, possibly via a role in posttranslational translocation; FRT1 has a paralog, FRT2, that arose from the whole genome duplication","termid":"PBO:0087801"}


id: GO:0051445
data:
  {"annotated_genes":["SJAG_04853","SJAG_01082","SJAG_02404","SJAG_03501","SJAG_03720","SJAG_03525","SJAG_04280","SJAG_04140","SJAG_05153","SJAG_05288","SJAG_04126","SJAG_02592","SJAG_03887","SJAG_04287","SJAG_02723","SJAG_00266","SJAG_03371","SJAG_01311","SJAG_01113","SJAG_01680","SJAG_03438","SJAG_02169","SJAG_04682","SJAG_00145","SJAG_01345","SJAG_01837","SJAG_01000","SJAG_01330","SJAG_00457","SJAG_03529","SJAG_01401","SJAG_04332","SJAG_02712","SJAG_00364","SJAG_03048","SJAG_01515","SJAG_04813","SJAG_01956","SJAG_02771","SJAG_03327","SJAG_06638","SJAG_04259","SJAG_00993","SJAG_03854","SJAG_02481","SJAG_00987","SJAG_03486"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89019,91339,92494,93575,103506],"is_not":false,"summary":null,"term":"GO:0051445"},{"annotations":[107125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010846"},{"annotations":[89551,108196,94350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051728"},{"annotations":[105477,113631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[105773,115193,90635],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[77255,115194,88268,113391,105774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051598"},{"annotations":[115802,100981,105478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033316"},{"annotations":[110342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[101546,103618,108416,117489,105807,105130,104972],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:0110045"},{"annotations":[115142,110707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110031"},{"annotations":[110343,115517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051447"},{"annotations":[97892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902103"},{"annotations":[107128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045128"},{"annotations":[101473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[89937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[115620,117355],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:0140648"},{"annotations":[93741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110032"},{"annotations":[88269,105779,115369,101558],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904514"},{"annotations":[112916],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:1905326"},{"annotations":[96241,106212,118212,101474,101560,118213,94352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051446"},{"annotations":[94353],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905191"},{"annotations":[88270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010845"},{"annotations":[91389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"},{"annotations":[100808,101570,93742,104077,108198],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0110044"},{"annotations":[100520],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:1905325"},{"annotations":[96134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0040020"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate or extent of progression through the meiotic cell cycle.","definition_xrefs":["GOC:ai","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle","termid":"GO:0051726"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"meiotic cell cycle","termid":"GO:0051321"}],"gene_count":47,"genes_by_uniquename":{"SJAG_00145":null,"SJAG_00266":null,"SJAG_00364":null,"SJAG_00457":null,"SJAG_00987":null,"SJAG_00993":null,"SJAG_01000":null,"SJAG_01082":null,"SJAG_01113":null,"SJAG_01311":null,"SJAG_01330":null,"SJAG_01345":null,"SJAG_01401":null,"SJAG_01515":null,"SJAG_01680":null,"SJAG_01837":null,"SJAG_01956":null,"SJAG_02169":null,"SJAG_02404":null,"SJAG_02481":null,"SJAG_02592":null,"SJAG_02712":null,"SJAG_02723":null,"SJAG_02771":null,"SJAG_03048":null,"SJAG_03327":null,"SJAG_03371":null,"SJAG_03438":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03525":null,"SJAG_03529":null,"SJAG_03720":null,"SJAG_03854":null,"SJAG_03887":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04332":null,"SJAG_04682":null,"SJAG_04813":null,"SJAG_04853":null,"SJAG_05153":null,"SJAG_05288":null,"SJAG_06638":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of meiotic cell cycle","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"meiotic cell cycle modulation","type":"exact"},{"name":"meiotic cell cycle regulation","type":"exact"},{"name":"meiotic cell cycle regulator","type":"related"},{"name":"modulation of meiotic cell cycle progression","type":"exact"},{"name":"regulation of meiotic cell cycle progression","type":"exact"},{"name":"regulation of progression through meiotic cell cycle","type":"exact"}],"termid":"GO:0051445","terms_by_termid":{"GO:0010845":null,"GO:0010846":null,"GO:0033315":null,"GO:0033316":null,"GO:0034307":null,"GO:0040020":null,"GO:0045128":null,"GO:0051445":null,"GO:0051446":null,"GO:0051447":null,"GO:0051598":null,"GO:0051728":null,"GO:0075296":null,"GO:0075297":null,"GO:0110031":null,"GO:0110032":null,"GO:0110044":null,"GO:0110045":null,"GO:0140648":null,"GO:1902103":null,"GO:1903024":null,"GO:1904514":null,"GO:1905191":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null}}


id: PBO:0067145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 193, pseudogene","termid":"PBO:0067145"}


id: PBO:0064065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 99","termid":"PBO:0064065"}


id: FYPO:0005239
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-tyrosine 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 tyrosine level","synonyms":[{"name":"increased cellular L-tyrosine level","type":"exact"},{"name":"increased cellular tyrosine level during mitotic cell cycle","type":"related"},{"name":"increased cellular tyrosine level during vegetative growth","type":"exact"},{"name":"increased tyrosine accumulation","type":"related"}],"termid":"FYPO:0005239"}


id: SO:0000613
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A DNA sequence to which bacterial RNA polymerase binds, to begin transcription.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prokaryotic_promoter","termid":"SO:0002222"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bacterial_RNApol_promoter","synonyms":[{"name":"bacterial RNApol promoter","type":"exact"}],"termid":"SO:0000613"}


id: PBO:0074779
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 3 pseudogene 1","termid":"PBO:0074779"}


id: GO:0010247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a phosphate ion stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of chemical stimulus","termid":"GO:0009593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of phosphate ion","synonyms":[{"name":"phosphate ion detection","type":"exact"},{"name":"phosphate ion perception","type":"related"},{"name":"phosphate ion sensing","type":"related"}],"termid":"GO:0010247"}


id: PBO:0030609
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_calcium_level","termid":"PBO:0030609"}


id: PR:O74449
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC16C4.04 gene.","definition_xrefs":["UniProtKB:O74449","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 C16C4.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16C4.04","synonyms":[{"name":"Spom972h-SPCC16C4.04","type":"exact"}],"termid":"PR:O74449"}


id: FYPO:0003053
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which homologous chromosome pairing during meiosis (synapsis) is increased (i.e. occurs to a greater extent) at a cis-acting homologous chromosome pairing region such as the sme2 locus.","definition_xrefs":["PomBase:mah","PMID:24173580","PMID:22582262","PMID:23117617"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal homologous chromosome pairing at cis-acting homologous chromosome pairing region","termid":"FYPO:0003052"}],"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":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000641"],"is_obsolete":false,"name":"increased homologous chromosome pairing at cis-acting homologous chromosome pairing region","synonyms":[{"name":"increased homologous chromosome pairing at meiosis at cis-acting homologous chromosome pairing region","type":"exact"},{"name":"increased homologous chromosome pairing at sme2 locus","type":"narrow"},{"name":"increased synapsis at cis-acting homologous chromosome pairing region","type":"exact"}],"termid":"FYPO:0003053"}


id: PBO:0046428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPH receptor B3","termid":"PBO:0046428"}


id: MONDO:0011811
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome is a rare hereditary ataxia characterized by a progressive cerebellar ataxia associated with disruption of visual fixation by saccadic intrusions (overshooting horizontal saccades with macrosaccadic oscillations and increased velocity of larger saccades). It presents with progressive gait, trunk and limb ataxia with pyramidal tract signs (increased tendon reflexes and Babinski sign), myoclonic jerks, fasciculations, cerebellar dysarthria, sensorimotor axonal neuropathy with impaired joint position, vibration, temperature, pain sensations, pes cavus, and saccadic intrusions with characteristic overshooting horizontal saccades, macrosaccadic oscillations, and increased velocity of larger saccades, without other eye movement disturbances.","definition_xrefs":["Orphanet:95434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive syndromic cerebellar ataxia","termid":"MONDO:0020047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive cerebellar ataxia-saccadic intrusion syndrome","secondary_identifiers":["OMIM:607317","DOID:0111611","MESH:C537310","GARD:4952","UMLS:C1846492","MEDGEN:335442"],"synonyms":[{"name":"SCAR4","type":"exact"},{"name":"SCASI","type":"exact"},{"name":"spinocerebellar ataxia 24","type":"related"},{"name":"spinocerebellar ataxia 24 (formerly)","type":"related"},{"name":"spinocerebellar ataxia 24, formerly","type":"related"},{"name":"spinocerebellar ataxia autosomal recessive 4","type":"related"},{"name":"spinocerebellar ataxia with saccadic Intrusions","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive 4","type":"related"}],"termid":"MONDO:0011811","xrefs":{"Monarch":{"xref_id":"0011811"}}}


id: MONDO:0019224
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An inherited metabolic disease that is has its basis in the disruption of gamma-aminobutyric acid metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"gene_count":0,"genotype_count":0,"name":"obsolete inborn disorder of gamma-aminobutyric acid metabolism (obsolete MONDO:0019224)","synonyms":[{"name":"disorder of GABA metabolism","type":"exact"},{"name":"disorder of gamma-aminobutyric acid metabolism","type":"related"},{"name":"inborn error of gamma-aminobutyric acid metabolic process","type":"exact"},{"name":"inborn gamma-aminobutyric acid metabolic process disorder","type":"exact"},{"name":"rare inborn error of gamma-aminobutyric acid metabolic process","type":"exact"}],"termid":"MONDO:0019224","xrefs":{"Monarch":{"xref_id":"0019224"}}}


id: GO:0046163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of heme C, a derivative of heme found in cytochromes c, b4, and f.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heme catabolic process","termid":"GO:0042167"},{"relation_name":"is_a","term_name":"heme C metabolic process","termid":"GO:0046162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"heme C catabolic process","synonyms":[{"name":"haem C catabolic process","type":"exact"},{"name":"haem C catabolism","type":"exact"},{"name":"heme C breakdown","type":"exact"},{"name":"heme C catabolism","type":"exact"},{"name":"heme C degradation","type":"exact"}],"termid":"GO:0046163"}


id: GO:0035469
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Determination of the asymmetric location of the pancreas with respect to the left and right halves of the organism.","definition_xrefs":["GOC:dgh","PMID:12702646"],"direct_ancestors":[{"relation_name":"is_a","term_name":"determination of left/right symmetry","termid":"GO:0007368"},{"relation_name":"part_of","term_name":"pancreas development","termid":"GO:0031016"}],"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":"determination of pancreatic left/right asymmetry","termid":"GO:0035469"}


id: GO:1990825
data:
  {"annotated_genes":["SJAG_00338"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90302],"is_not":false,"summary":null,"term":"GO:1990825"}]},"cv_name":"molecular_function","definition":"Binding to messenger RNA (mRNA) of a specific nucleotide composition or a specific sequence motif.","definition_xrefs":["PMID:11886857"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA binding","termid":"GO:0003729"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00338":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003723","GO:0005488"],"is_obsolete":false,"name":"sequence-specific mRNA binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990825","terms_by_termid":{"GO:1990825":null}}


id: GO:0016463
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + Zn2+(in) = ADP + phosphate + Zn2+(out).","definition_xrefs":["RHEA:20621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"zinc ion transmembrane transporter activity","termid":"GO:0005385"},{"relation_name":"is_a","term_name":"P-type ion transporter activity","termid":"GO:0015662"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"P-type zinc transporter activity","secondary_identifiers":["EC:7.2.2.12","MetaCyc:RXN0-5205"],"synonyms":[{"name":"ATP phosphohydrolase (Zn2+-exporting)","type":"exact"},{"name":"P(1B)-type ATPase activity","type":"narrow"},{"name":"P1B-type ATPase activity","type":"related"},{"name":"Zn(2+)-exporting ATPase activity","type":"related"},{"name":"Zn2+-exporting ATPase activity","type":"related"},{"name":"zinc exporting ATPase activity","type":"broad"},{"name":"zinc transmembrane transporter activity, phosphorylative mechanism","type":"related"},{"name":"zinc-exporting ATPase activity","type":"related"},{"name":"zinc-translocating P-type ATPase activity","type":"exact"}],"termid":"GO:0016463"}


id: PBO:0063847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PILR alpha associated neural protein","termid":"PBO:0063847"}


id: PBO:0040815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRD4 interacting chromatin remodeling complex associated protein","termid":"PBO:0040815"}


id: MONDO:1011846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypothalamic dysplasia, non-human animal","secondary_identifiers":["OMIA:000535"],"termid":"MONDO:1011846","xrefs":{"Monarch":{"xref_id":"1011846"}}}


id: MONDO:1012302
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylosis deformans, non-human animal","termid":"MONDO:1011955"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondylosis deformans, domestic cat","secondary_identifiers":["OMIA:001132-9685"],"termid":"MONDO:1012302","xrefs":{"Monarch":{"xref_id":"1012302"}}}


id: MONDO:0011158
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune lymphoproliferative syndrome","termid":"MONDO:0017979"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune lymphoproliferative syndrome type 1","secondary_identifiers":["OMIM:601859","SCTID:702444009","UMLS:C1328840","MEDGEN:231300","ICD9:279.41"],"synonyms":[{"name":"ALPS","type":"related"},{"name":"Canale-Smith syndrome","type":"related"},{"name":"autoimmune lymphoproliferative syndrome","type":"related"},{"name":"autoimmune lymphoproliferative syndrome type 1","type":"exact"},{"name":"autoimmune lymphoproliferative syndrome, type 1A","type":"narrow"},{"name":"autoimmune lymphoproliferative syndrome, type 1B","type":"narrow"},{"name":"autoimmune lymphoproliferative syndrome, type I, autosomal dominant","type":"related"},{"name":"autoimmune lymphoproliferative syndrome, type I, autosomal recessive","type":"related"},{"name":"autoimmune lymphoproliferative syndrome, type IA","type":"exact"},{"name":"autoimmune lymphoproliferative syndrome, type IB","type":"exact"}],"termid":"MONDO:0011158","xrefs":{"Monarch":{"xref_id":"0011158"}}}


id: PBO:0070108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 22 pseudogene","termid":"PBO:0070108"}


id: MONDO:0016554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare endocrine disease characterized by the appearance of transient hypothyroidism, usually in preterm newborns, following long or short-term topical iodine exposure. Parenteral exposure from iodinated contrast agents may similarly alter thyroid function in term neonates.","definition_xrefs":["Orphanet:238688"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"transient congenital hypothyroidism due to neonatal factor","termid":"MONDO:0016556"},{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neonatal iodine exposure","secondary_identifiers":["GARD:20644","UMLS:C4751432","MEDGEN:1669806"],"synonyms":[{"name":"iodine antenatal exposure","type":"related"}],"termid":"MONDO:0016554","xrefs":{"Monarch":{"xref_id":"0016554"}}}


id: GO:0018126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of a hydroxy group to a protein amino acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"}],"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":"protein hydroxylation","synonyms":[{"name":"protein amino acid hydroxylation","type":"exact"}],"termid":"GO:0018126"}


id: PBO:0047924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, folic acid type, rare, fra(11)(q23.3)","termid":"PBO:0047924"}


id: PBO:0051479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable (V)-58 (pseudogene)","termid":"PBO:0051479"}


id: PBO:0050656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein 90 alpha family class B member 6, pseudogene","termid":"PBO:0050656"}


id: FYPO:0007533
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 arrested replication forks colocalize normally (i.e. indistinguishably from wild type) with nuclear pore complexes (NPCs). Normally, arrested replication forks relocate to NPCs as part of replication fork processing, and remain anchored at NPCs while recombination-dependent replication takes place.","definition_xrefs":["PMID:33159083","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal replication fork processing","termid":"FYPO:0007254"}],"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:0000293"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0001312","FYPO:0000257","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal replication fork colocalization with nuclear pore complex","synonyms":[{"name":"normal replication fork colocalization with NPC","type":"exact"},{"name":"normal replication fork colocalization with nuclear pore","type":"exact"},{"name":"normal replication fork colocalization with nuclear pore complex during mitotic S phase","type":"exact"},{"name":"normal replication fork colocalization with nuclear pore complex during mitotic cell cycle","type":"related"},{"name":"normal replication fork colocalization with nuclear pore complex during vegetative growth","type":"exact"},{"name":"normal replication fork relocation to nuclear pore complex","type":"exact"},{"name":"normal replication fork relocation to nuclear pore complex during mitotic S phase","type":"exact"}],"termid":"FYPO:0007533"}


id: PBO:0047730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formin binding protein 1","termid":"PBO:0047730"}


id: PBO:0085288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peroxisomal ubiquitin conjugating enzyme; required for peroxisomal matrix protein import and peroxisome biogenesis","termid":"PBO:0085288"}


id: MONDO:0044205
data:
  {"annotated_genes":["SJAG_02171"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85225],"is_not":false,"summary":null,"term":"MONDO:0044205"}]},"cv_name":"mondo","definition":"Shwachman-Diamond syndrome-2 (SDS2) is characterized by exocrine pancreatic dysfunction, hematopoietic abnormalities, short stature, and metaphyseal dysplasia ({1:Stepensky et al., 2017}).nnFor a discussion of genetic heterogeneity of Shwachman-Diamond syndrome, see SDS1 (OMIM:260400).","definition_xrefs":["OMIM:617941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Shwachman-Diamond syndrome","termid":"MONDO:0009833"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02171":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Shwachman-Diamond syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1634617","UMLS:C4693704","GARD:16272"],"synonyms":[{"name":"SDS2","type":"related"},{"name":"Shwachman-Diamond syndrome 2","type":"exact"}],"termid":"MONDO:0044205","terms_by_termid":{"MONDO:0044205":null},"xrefs":{"Monarch":{"xref_id":"0044205"}}}


id: FYPO:0000374
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 RNA modification is increased. All RNA modification may be increased, or one or more specific RNA modifications may be selectively affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA modification","termid":"FYPO:0000370"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0000294","FYPO:0001985"],"is_obsolete":false,"name":"increased RNA modification","synonyms":[{"name":"RNA modification: increased","type":"related"},{"name":"increased RNA modification during mitotic cell cycle","type":"related"},{"name":"increased RNA modification during vegetative growth","type":"exact"}],"termid":"FYPO:0000374"}


id: MONDO:0011501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Skeletal dysplasia with wormian bone-multiple fractures-dentinogenesis imperfecta is a skeletal disorder, reported in three patients to date, characterized clinically by multiple fractures, wormian bones of the skull, dentinogenesis imperfecta and facial dysmorphism (hypertelorism, periorbital fullness). Although the signs are very similar to osteogenesis imperfecta, characteristic cortical defects in the absence of osteopenia and collagen abnormalities are considered to be distinctive. There have been no further descriptions in the literature since 1999.","definition_xrefs":["Orphanet:166277"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete malformative syndrome with dentinogenesis imperfecta (obsolete MONDO:0015877)","termid":"MONDO:0015877"},{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia","secondary_identifiers":["GARD:10290","MESH:C565734","UMLS:C1858032","OMIM:604922","MEDGEN:387969"],"synonyms":[{"name":"Suarez-Stickler syndrome","type":"exact"},{"name":"cortical defects wormian bones and dentinogenesis imperfecta","type":"related"},{"name":"cortical defects, WORMIAN bones, and dentinogenesis imperfecta","type":"related"}],"termid":"MONDO:0011501","xrefs":{"Monarch":{"xref_id":"0011501"}}}


id: FYPO:0003851
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 MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0002060","FYPO:0002058","FYPO:0000003","FYPO:0002057","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on MTT","synonyms":[{"name":"normal cell population growth in presence of MTT","type":"exact"},{"name":"normal cell population growth on MTT","type":"exact"},{"name":"normal cellular response to MTT","type":"related"},{"name":"normal growth on 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide","type":"exact"},{"name":"normal vegetative cell population growth on MTT","type":"exact"}],"termid":"FYPO:0003851"}


id: GO:0015076
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the directed movement of heavy metal ions into, out of or within a cell, or between cells. Heavy metals are those that can form a coordination bond with a protein, as opposed to an alkali or alkaline-earth metal that can only form an ionic bond; this definition includes the following biologically relevant heavy metals: Cd, Co, Cu, Fe, Hg, Mn, Mo, Ni, V, W, Zn.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete heavy metal ion transporter activity (obsolete GO:0015076)","synonyms":[{"name":"heavy metal ion transporter activity","type":"exact"}],"termid":"GO:0015076"}


id: GO:0005041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a low-density lipoprotein particle and delivering the low-density lipoprotein particle into the cell via endocytosis.","definition_xrefs":["GOC:bf","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle receptor activity","termid":"GO:0030228"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038024"}],"interesting_parent_ids":["GO:0038024","GO:0003674"],"is_obsolete":false,"name":"low-density lipoprotein particle receptor activity","secondary_identifiers":["Reactome:R-HSA-2424254","GO:0008032","Reactome:R-HSA-2404131","Wikipedia:LDL_receptor"],"synonyms":[{"name":"LDL receptor","type":"exact"},{"name":"LDLR activity","type":"exact"},{"name":"low-density lipoprotein receptor activity","type":"related"}],"termid":"GO:0005041"}


id: PBO:0071865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 3","termid":"PBO:0071865"}


id: PBO:0004576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Man5GlcNac2-PP-Dol translocation protein Rft1 (predicted)","termid":"PBO:0004576"}


id: PBO:0004198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-H (predicted)","termid":"PBO:0004198"}


id: FYPO:0003704
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of histone deacetylase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal histone deacetylase activity","termid":"FYPO:0003703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0001985","FYPO:0000654","FYPO:0000652","FYPO:0000661","FYPO:0005447","FYPO:0000002","FYPO:0000707"],"is_obsolete":false,"name":"decreased histone deacetylase activity","synonyms":[{"name":"reduced histone deacetylase activity","type":"exact"}],"termid":"FYPO:0003704"}


id: GO:0042184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of xylene, a mixture of three colorless, aromatic hydrocarbon liquids, ortho-, meta- and para-xylene.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xylene metabolic process","termid":"GO:0018948"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"hydrocarbon catabolic process","termid":"GO:0120253"}],"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":"xylene catabolic process","synonyms":[{"name":"xylene breakdown","type":"exact"},{"name":"xylene catabolism","type":"exact"},{"name":"xylene degradation","type":"exact"}],"termid":"GO:0042184"}


id: PR:Q9P7G3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAP14E8.05c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7G3"],"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":"TMEM14 protein homolog P14E8.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP14E8.05c","synonyms":[{"name":"Spom972h-SPAP14E8.05c","type":"exact"}],"termid":"PR:Q9P7G3"}


id: PBO:0065237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 13 pseudogene 5","termid":"PBO:0065237"}


id: PBO:0076446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAFA chemokine like family member 2","termid":"PBO:0076446"}


id: PBO:0030537
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_processing","termid":"PBO:0030537"}


id: GO:0039697
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A viral transcription process that uses negative stranded (-) single stranded (ss) RNA as a template.","definition_xrefs":["VZ:1096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA-templated viral transcription","termid":"GO:0039696"}],"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 stranded viral RNA transcription","termid":"GO:0039697"}


id: PBO:0055641
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 3080","termid":"PBO:0055641"}


id: GO:0050395
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-D-glucose + vitexin = H+ + UDP + vitexin 2''-O-beta-D-glucoside.","definition_xrefs":["EC:2.4.1.105","RHEA:21956"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"vitexin beta-glucosyltransferase activity","secondary_identifiers":["KEGG_REACTION:R03565","MetaCyc:VITEXIN-BETA-GLUCOSYLTRANSFERASE-RXN"],"synonyms":[{"name":"UDP-glucose:vitexin 2''-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:vitexin 2''-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-vitexin 2''-glucosyltransferase activity","type":"related"},{"name":"vitexin b-glucosyltransferase activity","type":"exact"}],"termid":"GO:0050395"}


id: GO:0044564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with a resultant blocking of a voltage-gated potassium channel, inhibiting the pore's activity, in the bitten/stung organism.","definition_xrefs":["GOC:fj","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in negative regulation of voltage-gated potassium channel activity in another organism","termid":"GO:0044562"}],"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":"envenomation resulting in occlusion of the pore of voltage-gated potassium channel in another organism","synonyms":[{"name":"envenomation resulting in occlusion of the pore of voltage-gated potassium channel in other organism","type":"exact"}],"termid":"GO:0044564"}


id: PBO:0029239
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_chromatin","termid":"PBO:0029239"}


id: MONDO:0014021
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial episodic pain syndrome","termid":"MONDO:0018319"}],"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":"familial episodic pain syndrome with predominantly upper body involvement","secondary_identifiers":["DOID:0111729","GARD:17618","MEDGEN:814997","OMIM:615040","Orphanet:391389","UMLS:C3808667"],"synonyms":[{"name":"FEPS1","type":"related"},{"name":"episodic pain syndrome, familial, 1","type":"related"},{"name":"episodic pain syndrome, familial, type 1","type":"exact"}],"termid":"MONDO:0014021","xrefs":{"Monarch":{"xref_id":"0014021"}}}


id: GO:1902958
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mitochondrial electron transport, NADH to ubiquinone.","definition_xrefs":["GOC:TermGenie","PMID:23530063","GOC:dph","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular respiration","termid":"GO:1901857"},{"relation_name":"is_a","term_name":"regulation of mitochondrial electron transport, NADH to ubiquinone","termid":"GO:1902956"},{"relation_name":"positively_regulates","term_name":"mitochondrial electron transport, NADH to ubiquinone","termid":"GO:0006120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006091"},{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"positive regulation of mitochondrial electron transport, NADH to ubiquinone","synonyms":[{"name":"activation of complex I (NADH to ubiquinone)","type":"related"},{"name":"activation of mitochondrial electron transport, NADH to ubiquinone","type":"narrow"},{"name":"activation of oxidative phosphorylation, NADH to ubiquinone","type":"narrow"},{"name":"positive regulation of complex I (NADH to ubiquinone)","type":"related"},{"name":"positive regulation of oxidative phosphorylation, NADH to ubiquinone","type":"exact"},{"name":"up regulation of complex I (NADH to ubiquinone)","type":"related"},{"name":"up regulation of mitochondrial electron transport, NADH to ubiquinone","type":"exact"},{"name":"up regulation of oxidative phosphorylation, NADH to ubiquinone","type":"exact"},{"name":"up-regulation of complex I (NADH to ubiquinone)","type":"related"},{"name":"up-regulation of mitochondrial electron transport, NADH to ubiquinone","type":"exact"},{"name":"up-regulation of oxidative phosphorylation, NADH to ubiquinone","type":"exact"},{"name":"upregulation of complex I (NADH to ubiquinone)","type":"related"},{"name":"upregulation of mitochondrial electron transport, NADH to ubiquinone","type":"exact"},{"name":"upregulation of oxidative phosphorylation, NADH to ubiquinone","type":"exact"}],"termid":"GO:1902958"}


id: PBO:0005086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBF1/Su(H)/LAG-1 family transcription factor Cbf11","termid":"PBO:0005086"}


id: PBO:0080812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-ray repair cross complementing 6 pseudogene 2","termid":"PBO:0080812"}


id: PBO:0041858
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase 4 like, pseudogene","termid":"PBO:0041858"}


id: PBO:0058039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4260","termid":"PBO:0058039"}


id: MOD:01609
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tryptophan residue to 7'-hydroxy-2'-alpha-mannosyl-L-tryptophan.","definition_xrefs":["RESID:AA0506","PubMed:19584055"],"direct_ancestors":[{"relation_name":"has_functional_parent","term_name":"2'-alpha-mannosyl-L-tryptophan","termid":"MOD:00222"},{"relation_name":"has_functional_parent","term_name":"7'-hydroxy-L-tryptophan","termid":"MOD:01664"},{"relation_name":"is_a","term_name":"modified L-tryptophan residue","termid":"MOD:00918"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"7'-hydroxy-2'-alpha-mannosyl-L-tryptophan","synonyms":[{"name":"(2S)-2-amino-3-[7-hydroxy-2-(alpha-D-mannopyranosyl)-1H-indol-3-yl]propanoic acid","type":"exact"},{"name":"7'-hydroxy-2'-alpha-mannosyl-L-tryptophan","type":"exact"},{"name":"CARBOHYD C-linked (Man) hydroxytryptophan","type":"exact"}],"termid":"MOD:01609"}


id: GO:0140691
data:
  {"annotated_genes":["SJAG_03460","SJAG_00886","SJAG_04266","SJAG_03070","SJAG_00195","SJAG_02469","SJAG_01819"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97684,106430,107695,112025,112958,114073,115007],"is_not":false,"summary":null,"term":"GO:0140691"}]},"cv_name":"molecular_function","definition":"Binding to an RNA or an RNA-containing complex to assist the folding process.","definition_xrefs":["PMID:31165735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00195":null,"SJAG_00886":null,"SJAG_01819":null,"SJAG_02469":null,"SJAG_03070":null,"SJAG_03460":null,"SJAG_04266":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"RNA folding chaperone","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140691","terms_by_termid":{"GO:0140691":null}}


id: GO:0008587
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the imaginal disc-derived wing margin are generated and organized. The wing margin is a strip of cells in the third instar disc at the boundary between the presumptive dorsal and ventral surfaces of the wing blade.","definition_xrefs":["GOC:bf","GOC:mtg_sensu","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"imaginal disc-derived wing morphogenesis","termid":"GO:0007476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"imaginal disc-derived wing margin morphogenesis","synonyms":[{"name":"wing margin morphogenesis","type":"exact"}],"termid":"GO:0008587"}


id: PBO:0051939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integral membrane protein 2A","termid":"PBO:0051939"}


id: PBO:0038320
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pubmed_entrez_date","termid":"PBO:0038320"}


id: GO:0048737
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an appendage over time, from its formation in the imaginal disc to the mature structure. An appendage is an organ or part that is attached to the trunk of an organism.","definition_xrefs":["GOC:mtg_sensu","GOC:rc","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"appendage development","termid":"GO:0048736"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"imaginal disc-derived appendage development","termid":"GO:0048737"}


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


id: PBO:0004380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase Ypt7","termid":"PBO:0004380"}


id: GO:0043950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process which activates, maintains or increases the frequency, rate or extent of cAMP-mediated signaling.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cAMP-mediated signaling","termid":"GO:0043949"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"cAMP-mediated signaling","termid":"GO:0019933"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of cAMP-mediated signaling","synonyms":[{"name":"positive regulation of cAMP-mediated signalling","type":"exact"}],"termid":"GO:0043950"}


id: PBO:0058131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4432 host gene","termid":"PBO:0058131"}


id: PATO:0001234
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's being located further from a more centrally located entity.","definition_xrefs":["PATOC:nw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal to","synonyms":[{"name":"distal","type":"exact"}],"termid":"PATO:0001234"}


id: GO:0006069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An ethanol metabolic process in which ethanol is converted to acetyl-CoA via acetaldehyde and acetate.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete ethanol oxidation (obsolete GO:0006069)","termid":"GO:0006069"}


id: GO:0070092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of glucagon.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of peptide hormone secretion","termid":"GO:0090276"},{"relation_name":"regulates","term_name":"glucagon secretion","termid":"GO:0070091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"regulation of glucagon secretion","termid":"GO:0070092"}


id: FYPO:0000974
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the cellular response to zinc ions is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular response to chemical stimulus during vegetative growth","termid":"FYPO:0001318"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0000298","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal cellular response to zinc ion","synonyms":[{"name":"normal cellular response to zinc","type":"exact"},{"name":"normal cellular response to zinc ion during mitotic cell cycle","type":"related"},{"name":"normal cellular response to zinc ion during vegetative growth","type":"exact"}],"termid":"FYPO:0000974"}


id: PBO:0036419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L7a involved in ribosome biogenesis","termid":"PBO:0036419"}


id: PBO:0059426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myocardin related transcription factor A","termid":"PBO:0059426"}


id: GO:2000727
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardiac muscle cell differentiation.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of striated muscle cell differentiation","termid":"GO:0051155"},{"relation_name":"is_a","term_name":"positive regulation of cardiocyte differentiation","termid":"GO:1905209"},{"relation_name":"is_a","term_name":"regulation of cardiac muscle cell differentiation","termid":"GO:2000725"},{"relation_name":"positively_regulates","term_name":"cardiac muscle cell differentiation","termid":"GO:0055007"}],"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 cardiac muscle cell differentiation","synonyms":[{"name":"positive regulation of cardiomyocyte differentiation","type":"exact"},{"name":"positive regulation of heart muscle cell differentiation","type":"related"}],"termid":"GO:2000727"}


id: MONDO:0006966
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition with a clinical picture similar to that of Parkinson disease, but which is caused by external factors, including medication.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"}],"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":"secondary Parkinson disease","secondary_identifiers":["MESH:D010302","NCIT:C34899","ICD9:332.1","SCTID:265377002","UMLS:C0030569","DOID:13548","EFO:1001175","MEDGEN:10592"],"synonyms":[{"name":"disorder presenting primarily with parkinsonism","type":"exact"},{"name":"secondary Parkinsonism","type":"exact"},{"name":"secondary parkinsonism (disorder) [ambiguous]","type":"exact"},{"name":"secondary parkinsonism, unspecified","type":"exact"},{"name":"symptomatic parkinsonism","type":"exact"}],"termid":"MONDO:0006966","xrefs":{"Monarch":{"xref_id":"0006966"}}}


id: PBO:0063744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 9","termid":"PBO:0063744"}


id: PBO:0051057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 3-9","termid":"PBO:0051057"}


id: MONDO:0011485
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive congenital ichthyosis characterized by fine white or greyish-white scales, hyperkeratosis, moderate acanthosis, and moderate parakeratosis that has material basis in homozygous mutation in the CYP4F22 gene on chromosome 19p13.","definition_xrefs":["PMID:16436457","PMID:10712223","DOID:0060714"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive congenital ichthyosis","termid":"MONDO:0017265"},{"relation_name":"is_a","term_name":"lamellar ichthyosis","termid":"MONDO:0017778"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005093"],"is_obsolete":false,"name":"autosomal recessive congenital ichthyosis 5","secondary_identifiers":["UMLS:C1858133","GARD:9734","MESH:C537265","OMIM:604777","MEDGEN:347628"],"synonyms":[{"name":"ARCI5","type":"exact"},{"name":"LI3, formerly","type":"related"},{"name":"NNCI","type":"related"},{"name":"autosomal recessive congenital ichthyosis 5","type":"exact"},{"name":"autosomal recessive congenital ichthyosis type 5","type":"exact"},{"name":"autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis","type":"exact"},{"name":"ichthyosis congenita 3","type":"related"},{"name":"ichthyosis congenita III","type":"related"},{"name":"ichthyosis lamellar 3","type":"related"},{"name":"ichthyosis, NONLAMELLAR and NONERYTHRODERMIC, congenital, autosomal recessive","type":"related"},{"name":"ichthyosis, Nonlamellar and Nonerythrodermic, congenital, autosomal recessive","type":"related"},{"name":"ichthyosis, congenital, autosomal recessive 5","type":"related"},{"name":"ichthyosis, congenital, autosomal recessive type 5","type":"exact"},{"name":"ichthyosis, lamellar, 3","type":"related"},{"name":"ichthyosis, lamellar, 3, formerly","type":"related"},{"name":"lamellar ichthyosis, type 3","type":"related"},{"name":"type 3 lamellar ichthyosis","type":"related"}],"termid":"MONDO:0011485","xrefs":{"Monarch":{"xref_id":"0011485"}}}


id: MOD:01462
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an L-proline alpha imino hydrogen with a methyl group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated proline","termid":"MOD:00712"},{"relation_name":"is_a","term_name":"alpha-amino methylated residue","termid":"MOD:01460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"N-methylated proline","termid":"MOD:01462"}


id: FYPO:0002368
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 trimethylation of lysine at position 4 of histone H3 occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased histone H3-K4 methylation during vegetative growth","termid":"FYPO:0002366"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0005447","FYPO:0002494","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased histone H3-K4 trimethylation during vegetative growth","synonyms":[{"name":"decreased histone H3 K4 trimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3-K4 trimethylation during mitotic cell cycle","type":"related"},{"name":"decreased histone H3K4 trimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3K4me3 during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K4 trimethylation during vegetative growth","type":"exact"},{"name":"reduced histone H3-K4 trimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002368"}


id: MONDO:0859286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures","secondary_identifiers":["OMIM:620029","DOID:0070536","MEDGEN:1823986","UMLS:C5774213"],"termid":"MONDO:0859286","xrefs":{"Monarch":{"xref_id":"0859286"}}}


id: MOD:01605
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to 5-glutamyl 2-aminoadipic acid.","definition_xrefs":["RESID:AA0502","ChEBI:78503","PubMed:19620981"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amidated residue","termid":"MOD:00674"},{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-glutamyl 2-aminoadipic acid","synonyms":[{"name":"(2S)-2-([(4S)-4-amino-4-carboxybutanoyl]amino)hexanedioic acid","type":"exact"},{"name":"5-glutamyl 2-aminoadipic acid","type":"exact"},{"name":"MOD_RES 5-glutamyl 2-aminoadipic acid","type":"exact"},{"name":"N2-(gamma-glutamyl)-2-aminoadipic acid","type":"exact"},{"name":"N2-(isoglutamyl)-2-aminoadipic acid","type":"exact"}],"termid":"MOD:01605"}


id: PBO:0090460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell surface fascilin domain protein, implicated in adhesion Mug57","termid":"PBO:0090460"}


id: PBO:0041364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 4 open reading frame 19","termid":"PBO:0041364"}


id: PBO:0088267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-myristoyltransferase Myr1","termid":"PBO:0088267"}


id: GO:1905356
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of snRNA pseudouridine synthesis.","definition_xrefs":["GOC:TermGenie","PMID:27268497","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of RNA metabolic process","termid":"GO:0051252"},{"relation_name":"regulates","term_name":"snRNA pseudouridine synthesis","termid":"GO:0031120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016073"}],"interesting_parent_ids":["GO:0008150","GO:0016073"],"is_obsolete":false,"name":"regulation of snRNA pseudouridine synthesis","termid":"GO:1905356"}


id: GO:0046171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of octanol, the 8-carbon alcohol with the formula C8H17OH.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"octanol metabolic process","termid":"GO:0006070"},{"relation_name":"is_a","term_name":"primary alcohol biosynthetic process","termid":"GO:0034309"},{"relation_name":"is_a","term_name":"fatty alcohol biosynthetic process","termid":"GO:1903175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"octanol biosynthetic process","synonyms":[{"name":"octanol anabolism","type":"exact"},{"name":"octanol biosynthesis","type":"exact"},{"name":"octanol formation","type":"exact"},{"name":"octanol synthesis","type":"exact"}],"termid":"GO:0046171"}


id: PBO:0061956
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily A member 12","termid":"PBO:0061956"}


id: PBO:0051214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 5-10-1","termid":"PBO:0051214"}


id: PBO:0071913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 52","termid":"PBO:0071913"}


id: MONDO:0014673
data:
  {"annotated_genes":["SJAG_00624"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84319],"is_not":false,"summary":null,"term":"MONDO:0014673"}]},"cv_name":"mondo","definition":"Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the LSS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset non-syndromic cataract","termid":"MONDO:0011060"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00624":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cataract 44","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4225300","DOID:0110267","GARD:16127","OMIM:616509","MEDGEN:907487"],"synonyms":[{"name":"CTRCT44","type":"exact"},{"name":"LSS early-onset non-syndromic cataract","type":"exact"},{"name":"cataract 44","type":"exact"},{"name":"cataract type 44","type":"exact"},{"name":"early-onset non-syndromic cataract caused by mutation in LSS","type":"exact"},{"name":"total early-onset cataract","type":"broad"}],"termid":"MONDO:0014673","terms_by_termid":{"MONDO:0014673":null},"xrefs":{"Monarch":{"xref_id":"0014673"}}}


id: PBO:0062785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ORAI calcium release-activated calcium modulator 3","termid":"PBO:0062785"}


id: MONDO:0004687
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"background diabetic retinopathy","termid":"MONDO:0001661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"severe nonproliferative diabetic retinopathy","secondary_identifiers":["icd11.foundation:561966379","SCTID:312905005","MEDGEN:676487","ICD9:362.06","DOID:8946","UMLS:C0730278"],"synonyms":[{"name":"high risk non proliferative diabetic retinopathy","type":"exact"},{"name":"severe NPDR","type":"exact"},{"name":"severe nonproliferative diabetic retinopathy","type":"exact"},{"name":"severe nonproliferative retinopathy","type":"related"},{"name":"severe npdr","type":"related"}],"termid":"MONDO:0004687","xrefs":{"Monarch":{"xref_id":"0004687"}}}


id: PBO:0000893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-binding protein (predicted)","termid":"PBO:0000893"}


id: MONDO:0019035
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pancreatoblastoma is a rare malignant epithelial pancreatic neoplasm, most often found in children, which usually presents with the non-specific symptoms of a palpable mass, vomiting abdominal pain, jaundice, and weight loss/failure to thrive, and is characterized histologically by multiple lines of differentiation (acinar, ductal, mesenchymal, neuroendocrine) and the presence of squamoid nests.","definition_xrefs":["Orphanet:677"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant exocrine pancreas neoplasm","termid":"MONDO:0002116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"pancreatoblastoma","secondary_identifiers":["UMLS:C0334489","ONCOTREE:PB","DOID:6823","MESH:C537162","NANDO:2200082","GARD:4210","icd11.foundation:733863058","MEDGEN:87250","NCIT:C4265","icd11.foundation:1310236105"],"synonyms":[{"name":"PB","type":"related"},{"name":"pancreatoblastoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0019035","xrefs":{"Monarch":{"xref_id":"0019035"}}}


id: FYPO:0004147
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of pyridoxine:NADP 4-dehydrogenase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal pyridoxine:NADP 4-dehydrogenase activity","termid":"FYPO:0004145"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000654","FYPO:0000707","FYPO:0000652","FYPO:0000661"],"is_obsolete":false,"name":"increased pyridoxine:NADP 4-dehydrogenase activity","termid":"FYPO:0004147"}


id: PBO:0016075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongator complex subunit Elp3 (predicted)","termid":"PBO:0016075"}


id: GO:0000009
data:
  {"annotated_genes":["SJAG_03555","SJAG_00437","SJAG_00816","SJAG_03056","SJAG_00295","SJAG_04770","SJAG_01276"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[86722,86723,97081,104113,111833],"is_not":false,"summary":null,"term":"GO:0000009"},{"annotations":[104164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052917"},{"annotations":[101484],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102704"},{"annotations":[86724,90430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033164"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a mannose residue to an oligosaccharide, forming an alpha-(1->6) linkage.","definition_xrefs":["GOC:mcc","PMID:2644248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannosyltransferase activity","termid":"GO:0000030"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00295":null,"SJAG_00437":null,"SJAG_00816":null,"SJAG_01276":null,"SJAG_03056":null,"SJAG_03555":null,"SJAG_04770":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016757"],"is_obsolete":false,"name":"alpha-1,6-mannosyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-449718"],"synonyms":[{"name":"1,6-alpha-mannosyltransferase activity","type":"exact"}],"termid":"GO:0000009","terms_by_termid":{"GO:0000009":null,"GO:0033164":null,"GO:0052917":null,"GO:0102704":null}}


id: FYPO:0006396
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which interphase microtubule organizing center (iMTOC) assembly is abnormal. iMTOC assembly is the aggregation, arrangement and bonding together of a set of components to form an interphase microtubule organizing center.","definition_xrefs":["GO:0031024","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton organization during vegetative growth","termid":"FYPO:0001350"},{"relation_name":"is_a","term_name":"abnormal cellular component assembly during vegetative growth","termid":"FYPO:0001354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000054","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abnormal iMTOC assembly","synonyms":[{"name":"abnormal iMTOC assembly during mitotic cell cycle","type":"related"},{"name":"abnormal iMTOC assembly during vegetative growth","type":"exact"},{"name":"abnormal iMTOC formation","type":"exact"},{"name":"abnormal interphase microtubule organizing center assembly","type":"exact"},{"name":"abnormal interphase microtubule organizing center formation","type":"exact"}],"termid":"FYPO:0006396"}


id: GO:0034667
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An integrin complex that comprises one alpha3 subunit and one beta1 subunit.","definition_xrefs":["PMID:12297042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integrin complex","termid":"GO:0008305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"integrin alpha3-beta1 complex","synonyms":[{"name":"ITGA3-ITGB1 complex","type":"narrow"},{"name":"VLA-3 complex","type":"exact"},{"name":"alpha3-beta1 integrin complex","type":"exact"}],"termid":"GO:0034667"}


id: PBO:0087358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Splicing factor that reanneals snRNPs during spliceosome recycling; reanneals U4 and U6 snRNPs","termid":"PBO:0087358"}


id: GO:0070375
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A MAPK cascade containing at least the ERK5 MAP kinase (MAPK7; also called BMK1). It starts with the activation of a MAP3K, and the consecutive activation of a MPK2K and of ERK5. The cascade can also contain an additional tier: the upstream MAP4K. The kinases in each tier phosphorylate and activate the kinases in the downstream tier. The ERK5 cascade is activated by stress, mitogens, and by G protein-coupled receptors, and results in cellular responses such as cell growth, cell differentiation and development.","definition_xrefs":["PMID:16880823","PMID:28903453","PMID:16376520","PMID:20811974","PMID:23125017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"MAPK cascade","termid":"GO:0000165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"ERK5 cascade","synonyms":[{"name":"BMK cascade","type":"exact"},{"name":"BMK signaling pathway","type":"exact"},{"name":"BMK signalling pathway","type":"exact"},{"name":"BMK1 cascade","type":"exact"},{"name":"ERK5 signaling pathway","type":"exact"},{"name":"MAPK7 cascade","type":"exact"},{"name":"big MAP kinase signaling cascade","type":"exact"},{"name":"extracellular signal-regulated kinase 5 cascade","type":"exact"}],"termid":"GO:0070375"}


id: PR:Q9Y7V2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC645.13 gene.","definition_xrefs":["UniProtKB:Q9Y7V2","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 bye1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC645.13","synonyms":[{"name":"Spom972h-SPCC645.13","type":"exact"}],"termid":"PR:Q9Y7V2"}


id: GO:0035808
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that initiates the formation of double-strand breaks (DSBs) required for meiotic recombination. Consists of a protein that catalyses formation of the double-strand breaks (Spo11 in S. cerevisiae and Rec12 in S. pombe), and a number of accessory proteins.","definition_xrefs":["PMID:12897161","GOC:vw","PMID:20364342","PMID:21429938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"condensed nuclear chromosome","termid":"GO:0000794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"meiotic recombination initiation complex","termid":"GO:0035808"}


id: PBO:0035957
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_checkpoint_complex_assembly","termid":"PBO:0035957"}


id: GO:0051787
data:
  {"annotated_genes":["SJAG_00354"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76448],"is_not":false,"summary":null,"term":"GO:0051787"}]},"cv_name":"molecular_function","definition":"Binding to a misfolded protein.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00354":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"misfolded protein binding","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-5324632"],"termid":"GO:0051787","terms_by_termid":{"GO:0051787":null}}


id: PBO:0040664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bardet-Biedl syndrome 10","termid":"PBO:0040664"}


id: PBO:0057142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 221","termid":"PBO:0057142"}


id: GO:0043573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation of two or more leucoplasts by division of one leucoplast. A leucoplast is a colorless plastid involved in the synthesis of monoterpenes.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid fission","termid":"GO:0043572"}],"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":"leucoplast fission","termid":"GO:0043573"}


id: MONDO:1011767
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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":"laminitis, non-human animal","secondary_identifiers":["OMIA:001225"],"termid":"MONDO:1011767","xrefs":{"Monarch":{"xref_id":"1011767"}}}


id: GO:0090332
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of closing of stomata, pores in the epidermis of leaves and stems bordered by two guard cells and serving in gas exchange.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stomatal movement","termid":"GO:0010118"}],"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":"stomatal closure","termid":"GO:0090332"}


id: GO:1990653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a monounsaturated fatty acid. A monounsaturated fatty acid has one double bond in the fatty acid chain with all of the remainder carbon atoms being single-bonded, as opposed to polyunsaturated fatty acids.","definition_xrefs":["PMID:16443825","GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete monounsaturated fatty acid biosynthetic process (obsolete GO:1990653)","termid":"GO:1990653"}


id: GO:0017164
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nicotinic acetylcholine receptor-associated protein activity (obsolete GO:0017164)","synonyms":[{"name":"nicotinic acetylcholine receptor-associated protein activity","type":"exact"}],"termid":"GO:0017164"}


id: GO:2000296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of hydrogen peroxide catabolic process.","definition_xrefs":["GOC:BHF"],"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 hydrogen peroxide metabolic process","termid":"GO:0010727"},{"relation_name":"is_a","term_name":"regulation of hydrogen peroxide catabolic process","termid":"GO:2000295"},{"relation_name":"negatively_regulates","term_name":"hydrogen peroxide catabolic process","termid":"GO:0042744"}],"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 hydrogen peroxide catabolic process","synonyms":[{"name":"negative regulation of H2O2 catabolic process","type":"exact"},{"name":"negative regulation of H2O2 scavenging","type":"related"},{"name":"negative regulation of detoxification of H2O2","type":"related"},{"name":"negative regulation of detoxification of hydrogen peroxide","type":"related"},{"name":"negative regulation of hydrogen peroxide breakdown","type":"exact"},{"name":"negative regulation of hydrogen peroxide catabolism","type":"exact"},{"name":"negative regulation of hydrogen peroxide degradation","type":"exact"},{"name":"negative regulation of hydrogen peroxide removal","type":"related"},{"name":"negative regulation of hydrogen peroxide scavenging","type":"related"}],"termid":"GO:2000296"}


id: PBO:0068491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 75, pseudogene","termid":"PBO:0068491"}


id: PBO:0017837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"predicted GTPAse with a role in RNA polymerase localization (predicted)","termid":"PBO:0017837"}


id: GO:0097268
data:
  {"annotated_genes":["SJAG_05024"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[86993],"is_not":false,"summary":null,"term":"GO:0097268"}]},"cv_name":"cellular_component","definition":"A subcellular filamentary structure where CTP synthase is compartmentalized in a range of organisms including bacteria, yeast, fruit fly, rat and human.","definition_xrefs":["PMID:21930098","GOC:mag","PMID:20513629","Wikipedia:CTP_synthase#Cytoophidium"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supramolecular fiber","termid":"GO:0099512"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05024":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"cytoophidium","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0097268","terms_by_termid":{"GO:0097268":null}}


id: GO:0030450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the classical pathway of complement activation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of humoral immune response mediated by circulating immunoglobulin","termid":"GO:0002923"},{"relation_name":"is_a","term_name":"regulation of complement activation","termid":"GO:0030449"},{"relation_name":"regulates","term_name":"complement activation, classical pathway","termid":"GO:0006958"}],"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 complement activation, classical pathway","synonyms":[{"name":"regulation of complement cascade, classical pathway","type":"exact"}],"termid":"GO:0030450"}


id: PBO:0077344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 86A","termid":"PBO:0077344"}


id: GO:0021547
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process that gives rise to the midbrain-hindbrain boundary. The midbrain-hindbrain domain of the embryonic brain is comprised of the mesencephalic vesicle and the first rhombencephalic vesicle at early somitogenesis stages. An organizing center at the boundary patterns the midbrain and hindbrain primordia of the neural plate.","definition_xrefs":["GOC:dgh","GO_REF:0000021","GOC:dph","GOC:isa_complete","GOC:jid","PMID:15541513","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"is_a","term_name":"formation of anatomical boundary","termid":"GO:0048859"},{"relation_name":"part_of","term_name":"neural plate anterior/posterior regionalization","termid":"GO:0021999"},{"relation_name":"part_of","term_name":"midbrain-hindbrain boundary development","termid":"GO:0030917"}],"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":"midbrain-hindbrain boundary initiation","synonyms":[{"name":"MHB biosynthesis","type":"exact"},{"name":"MHB formation","type":"exact"},{"name":"isthmus biosynthesis","type":"related"},{"name":"isthmus formation","type":"related"},{"name":"midbrain-hindbrain boundary biosynthesis","type":"exact"},{"name":"midbrain-hindbrain boundary formation","type":"exact"}],"termid":"GO:0021547"}


id: PBO:0078350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon CTC) 16-1","termid":"PBO:0078350"}


id: GO:0043918
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cadaverine + S-adenosyl 3-(methylsulfanyl)propylamine = aminopropylcadaverine + H+ + S-methyl-5'-thioadenosine.","definition_xrefs":["PMID:17545282","RHEA:33387"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016765"}],"interesting_parent_ids":["GO:0016765","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"cadaverine aminopropyltransferase activity","synonyms":[{"name":"cadaverine aminopropyl transferase activity","type":"exact"}],"termid":"GO:0043918"}


id: PBO:0063277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin gamma subfamily A, 3","termid":"PBO:0063277"}


id: MONDO:0002001
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disease of cellular proliferation (obsolete MONDO:0002001)","termid":"MONDO:0002001","xrefs":{"Monarch":{"xref_id":"0002001"}}}


id: GO:0061265
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the cells of the mesonephric nephron tubule as it progresses from its formation to the mature state.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation involved in mesonephros development","termid":"GO:0061208"},{"relation_name":"is_a","term_name":"nephron tubule epithelial cell differentiation","termid":"GO:0072160"},{"relation_name":"part_of","term_name":"mesonephric nephron tubule development","termid":"GO:0061242"}],"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":"mesonephric nephron tubule epithelial cell differentiation","termid":"GO:0061265"}


id: GO:0090149
data:
  {"annotated_genes":["SJAG_02848","SJAG_05261","SJAG_03464"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94164,101689,101945],"is_not":false,"summary":null,"term":"GO:0090149"}]},"cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the separation of a single continuous mitochondrial membrane into two membranes and contributes to mitochondrial fission.","definition_xrefs":["GOC:dph","GOC:ascb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane fission","termid":"GO:0090148"},{"relation_name":"part_of","term_name":"mitochondrial fission","termid":"GO:0000266"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02848":null,"SJAG_03464":null,"SJAG_05261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007005","GO:0061024"],"is_obsolete":false,"name":"mitochondrial membrane fission","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"membrane fission involved in mitochondrial fission","type":"exact"},{"name":"mitochondrial membrane scission","type":"exact"}],"termid":"GO:0090149","terms_by_termid":{"GO:0090149":null}}


id: PBO:0084762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial mitophagy-specific protein; required primarily for mitophagy induced at post-log phase; not required for other types of selective autophagy or macroautophagy; conserved within fungi, but not in higher eukaryotes; ATG33 has a paralog, SCM4, that arose from the whole genome duplication","termid":"PBO:0084762"}


id: GO:2000411
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of thymocyte migration.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell migration","termid":"GO:2000405"},{"relation_name":"is_a","term_name":"regulation of thymocyte migration","termid":"GO:2000410"},{"relation_name":"negatively_regulates","term_name":"thymocyte migration","termid":"GO:0072679"}],"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 thymocyte migration","synonyms":[{"name":"negative regulation of immature T cell migration","type":"related"},{"name":"negative regulation of immature T lymphocyte migration","type":"related"},{"name":"negative regulation of immature T-cell migration","type":"related"},{"name":"negative regulation of immature T-lymphocyte migration","type":"related"},{"name":"negative regulation of thymic lymphocyte migration","type":"exact"}],"termid":"GO:2000411"}


id: PBO:0068946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 190, pseudogene","termid":"PBO:0068946"}


id: GO:0061238
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Coordinated organization of groups of cells in the plane of an epithelium that contributes to the shaping of a nephron in the mesonephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of planar polarity involved in nephron morphogenesis","termid":"GO:0072046"},{"relation_name":"part_of","term_name":"mesonephric nephron morphogenesis","termid":"GO:0061228"}],"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":"establishment of planar polarity involved in mesonephric nephron morphogenesis","synonyms":[{"name":"establishment of planar cell polarity involved in mesonephric nephron morphogenesis","type":"narrow"}],"termid":"GO:0061238"}


id: GO:0031305
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the mitochondrial inner membrane consisting of the gene products having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of mitochondrial inner membrane (obsolete GO:0031305)","synonyms":[{"name":"integral to mitochondrial inner membrane","type":"narrow"}],"termid":"GO:0031305"}


id: PBO:0070665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 36","termid":"PBO:0070665"}


id: GO:0070668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the rate or extent of mast cell proliferation.","definition_xrefs":["GOC:add","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte proliferation","termid":"GO:0070665"},{"relation_name":"is_a","term_name":"regulation of mast cell proliferation","termid":"GO:0070666"},{"relation_name":"positively_regulates","term_name":"mast cell proliferation","termid":"GO:0070662"}],"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 mast cell proliferation","synonyms":[{"name":"activation of mast cell proliferation","type":"narrow"},{"name":"stimulation of mast cell proliferation","type":"narrow"},{"name":"up regulation of mast cell proliferation","type":"exact"},{"name":"up-regulation of mast cell proliferation","type":"exact"},{"name":"upregulation of mast cell proliferation","type":"exact"}],"termid":"GO:0070668"}


id: SO:0001151
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A motif of four consecutive peptide residues, of which the i+2 residue is proline, and that may contain one H-bond, which, if present, is between the main-chain CO of the first residue and the main-chain NH of the fourth and is characterized by the dihedral angles: Residue(i+1): phi ~ -60 degrees, psi ~ 120 degrees. Residue(i+2): phi ~ -90 degrees, psi ~ 0 degrees.","definition_xrefs":["PMID:2371257","SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta_turn_type_six","termid":"SO:0001150"}],"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":"beta_turn_type_six_a","synonyms":[{"name":"beta turn type six a","type":"exact"},{"name":"type VIa beta turn","type":"exact"},{"name":"type VIa turn","type":"exact"}],"termid":"SO:0001151"}


id: FYPO:0008273
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of histone H4 binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type). The affected gene product may be encoded by the mutated gene, or by a different gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone binding","termid":"FYPO:0008271"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000702","FYPO:0000257"],"is_obsolete":false,"name":"normal histone H4 binding","termid":"FYPO:0008273"}


id: PR:O13877
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerases I, II, and III subunit RPABC5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02059","PANTHER:PTHR23413:SF2","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":"DNA-directed RNA polymerases I, II, and III subunit RPABC5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B3.12c","secondary_identifiers":["UniProtKB:O13877"],"synonyms":[{"name":"ABC10-beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DNA-directed RNA polymerases I, II, and III 8.3 kDa polypeptide (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerases I, II, and III subunit ABC5 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RPC8 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-POLR2L","type":"exact"}],"termid":"PR:O13877"}


id: PBO:0038431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aladin WD repeat nucleoporin","termid":"PBO:0038431"}


id: PBO:0085524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the small (40S) ribosomal subunit; homologous to mammalian ribosomal protein S25, no bacterial homolog; RPS25B has a paralog, RPS25A, that arose from the whole genome duplication","termid":"PBO:0085524"}


id: MONDO:1012510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"facial dysplasia syndrome, non-human animal","termid":"MONDO:1011656"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"facial dysplasia syndrome, cattle","secondary_identifiers":["OMIA:002090-9913"],"termid":"MONDO:1012510","xrefs":{"Monarch":{"xref_id":"1012510"}}}


id: MONDO:0003363
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the dermis.","direct_ancestors":[{"relation_name":"is_a","term_name":"dermis tumor","termid":"MONDO:0002300"},{"relation_name":"is_a","term_name":"skin cancer","termid":"MONDO:0002898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"malignant dermis tumor","secondary_identifiers":["MEDGEN:87564","DOID:5274","NCIT:C4574","SCTID:255096006","UMLS:C0346811"],"synonyms":[{"name":"cancer of dermis","type":"exact"},{"name":"dermis cancer","type":"exact"},{"name":"malignant dermal neoplasm","type":"exact"},{"name":"malignant dermis neoplasm","type":"exact"},{"name":"malignant dermis tumor","type":"exact"},{"name":"malignant neoplasm of dermis","type":"exact"},{"name":"malignant neoplasm of the dermis","type":"exact"},{"name":"malignant tumor of dermis","type":"exact"},{"name":"malignant tumor of the dermis","type":"exact"},{"name":"malignant tumour of dermis","type":"exact"},{"name":"malignant tumour of the dermis","type":"exact"}],"termid":"MONDO:0003363","xrefs":{"Monarch":{"xref_id":"0003363"}}}


id: GO:1990229
data:
  {"annotated_genes":["SJAG_03701","SJAG_03862","SJAG_04016","SJAG_02895","SJAG_00532","SJAG_02497","SJAG_00894","SJAG_00186","SJAG_02306","SJAG_03222","SJAG_04397","SJAG_02994","SJAG_02866","SJAG_01238","SJAG_01063","SJAG_00040"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[98128,99217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904564"},{"annotations":[86853,99218,113895,88175],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097361"},{"annotations":[92156,92384,102281,113003,97458,108832,106035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099128"},{"annotations":[116980,91973,103930,109013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120510"}]},"cv_name":"cellular_component","definition":"A protein complex capable of assembling an iron-sulfur (Fe-S) cluster.","definition_xrefs":["GOC:bhm","PMID:17350958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00040":null,"SJAG_00186":null,"SJAG_00532":null,"SJAG_00894":null,"SJAG_01063":null,"SJAG_01238":null,"SJAG_02306":null,"SJAG_02497":null,"SJAG_02866":null,"SJAG_02895":null,"SJAG_02994":null,"SJAG_03222":null,"SJAG_03701":null,"SJAG_03862":null,"SJAG_04016":null,"SJAG_04397":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0005737","GO:0005829","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"iron-sulfur cluster assembly complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Fe-S cluster assembly complex","type":"narrow"},{"name":"SufBCD complex","type":"narrow"}],"termid":"GO:1990229","terms_by_termid":{"GO:0097361":null,"GO:0099128":null,"GO:0120510":null,"GO:1904564":null}}


id: MONDO:0009256
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Excessive or inappropriate lactation in females or males, and not necessarily related to pregnancy. Galactorrhea can occur either unilaterally or bilaterally, and be profuse or sparse. Its most common cause is hyperprolactinemia.","definition_xrefs":["MESH:D005687"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lactation disease","termid":"MONDO:0045019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactorrhea","secondary_identifiers":["NCIT:C113343","ICD9:611.6","SCTID:78622004","HP:0100829","MEDGEN:777088","UMLS:C3665358"],"synonyms":[{"name":"galactorrhea","type":"exact"},{"name":"galactorrhea (disease)","type":"exact"}],"termid":"MONDO:0009256","xrefs":{"Monarch":{"xref_id":"0009256"}}}


id: PBO:0036341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic protein, human C2orf76 ortholog, implicated in mitochondrial organisation","termid":"PBO:0036341"}


id: FYPO:0007376
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a region of the genome that is normally stably assembled and maintained as heterochromatin over successive generations entirely loses heterochromatic structure.","definition_xrefs":["PMID:29899117","PMID:31278118","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal epigenetic heterochromatin inheritance","termid":"FYPO:0007477"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0007477"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0007477","FYPO:0001985"],"is_obsolete":false,"name":"abolished epigenetic heterochromatin inheritance","synonyms":[{"name":"abolished PEV","type":"related"},{"name":"abolished epigenetic heterochromatin propagation","type":"exact"},{"name":"abolished epigenetic inheritance of heterochromatin","type":"exact"}],"termid":"FYPO:0007376"}


id: PBO:0064339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDX1 associated lncRNA, upregulator of transcription","termid":"PBO:0064339"}


id: PBO:0081109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFAND2A divergent transcript","termid":"PBO:0081109"}


id: PBO:0053109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine carboxyl methyltransferase 1","termid":"PBO:0053109"}


id: GO:0070781
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 biotin stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to organic cyclic compound","termid":"GO:0014070"},{"relation_name":"is_a","term_name":"response to vitamin","termid":"GO:0033273"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to biotin","synonyms":[{"name":"response to Bios IIB","type":"exact"},{"name":"response to coenzyme R","type":"exact"},{"name":"response to vitamin B7","type":"exact"},{"name":"response to vitamin H","type":"exact"}],"termid":"GO:0070781"}


id: GO:0044423
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any constituent part of a virion, a complete fully infectious extracellular virus particle.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular_component","termid":"GO:0005575"}],"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":"virion component","secondary_identifiers":["Wikipedia:Virus","GO:0019012"],"synonyms":[{"name":"complete virus particle","type":"related"},{"name":"virion","type":"related"},{"name":"virion part","type":"exact"}],"termid":"GO:0044423"}


id: PBO:0017763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intramembrane aspartyl protease of the perinuclear ER membrane Ypf1 (predicted)","termid":"PBO:0017763"}


id: PBO:0071588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 5","termid":"PBO:0071588"}


id: GO:0018379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The linkage of cytochromes and other heme proteins to heme via heme-bis-L-cysteine.","definition_xrefs":["RESID:AA0134"],"gene_count":0,"genotype_count":0,"name":"obsolete cytochrome c-heme linkage via heme-bis-L-cysteine (obsolete GO:0018379)","synonyms":[{"name":"cytochrome c-haem linkage via haem-bis-L-cysteine","type":"exact"}],"termid":"GO:0018379"}


id: MONDO:0004920
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrocele","secondary_identifiers":["MEDGEN:318568","DOID:9912","ICD9:603.9","ICD9:603.8","SCTID:55434001","UMLS:C1720771"],"termid":"MONDO:0004920","xrefs":{"Monarch":{"xref_id":"0004920"}}}


id: GO:0008781
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: CTP + N-acylneuraminate = diphosphate + CMP-N-acylneuraminate.","definition_xrefs":["EC:2.7.7.43"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytidylyltransferase activity","termid":"GO:0070567"}],"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:0016779"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016779","GO:0016740"],"is_obsolete":false,"name":"N-acylneuraminate cytidylyltransferase activity","secondary_identifiers":["Reactome:R-HSA-4084982","RHEA:11344","MetaCyc:RXN-9990"],"synonyms":[{"name":"CMP-N-acetylneuraminate synthase activity","type":"related"},{"name":"CMP-N-acetylneuraminate synthetase activity","type":"related"},{"name":"CMP-N-acetylneuraminic acid synthase activity","type":"related"},{"name":"CMP-N-acetylneuraminic acid synthetase activity","type":"related"},{"name":"CMP-NANA synthetase activity","type":"related"},{"name":"CMP-Neu5Ac synthetase activity","type":"related"},{"name":"CMP-NeuAc synthetase activity","type":"related"},{"name":"CMP-NeuNAc synthetase activity","type":"related"},{"name":"CMP-sialate diphosphorylase activity","type":"related"},{"name":"CMP-sialate pyrophosphorylase activity","type":"related"},{"name":"CMP-sialate synthase activity","type":"related"},{"name":"CMP-sialate synthetase activity","type":"related"},{"name":"CMP-sialic acid synthetase activity","type":"related"},{"name":"CMP-sialic synthetase activity","type":"related"},{"name":"CTP:N-acylneuraminate cytidylyltransferase activity","type":"exact"},{"name":"acetylneuraminate cytidylyltransferase activity","type":"related"},{"name":"acylneuraminate cytidyltransferase activity","type":"related"},{"name":"cytidine 5'-monophospho-N-acetylneuraminic acid synthetase activity","type":"related"},{"name":"cytidine 5'-monophosphosialic acid synthetase activity","type":"related"},{"name":"cytidine 5-monophosphate N-acetylneuraminic acid synthetase activity","type":"related"},{"name":"cytidine monophosphoacetylneuraminic synthetase activity","type":"related"},{"name":"cytidine monophosphosialate pyrophosphorylase activity","type":"related"},{"name":"cytidine monophosphosialate synthetase activity","type":"related"},{"name":"cytidine monophosphosialic acid synthetase activity","type":"related"}],"termid":"GO:0008781"}


id: GO:0047810
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-alanine + 2-oxoglutarate = pyruvate + D-glutamate.","definition_xrefs":["EC:2.6.1.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016769","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"D-alanine-2-oxoglutarate aminotransferase activity","secondary_identifiers":["MetaCyc:D-ALANINE-AMINOTRANSFERASE-RXN","RHEA:15869"],"synonyms":[{"name":"D-alanine aminotransferase activity","type":"exact"},{"name":"D-alanine transaminase activity","type":"broad"},{"name":"D-alanine-D-glutamate transaminase activity","type":"related"},{"name":"D-amino acid aminotransferase activity","type":"broad"},{"name":"D-amino acid transaminase activity","type":"broad"},{"name":"D-amino-acid transaminase activity","type":"broad"},{"name":"D-aspartate aminotransferase activity","type":"related"},{"name":"D-aspartate transaminase activity","type":"related"},{"name":"D-aspartic aminotransferase activity","type":"related"}],"termid":"GO:0047810"}


id: GO:0045666
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of neuron differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of neuron differentiation","termid":"GO:0045664"},{"relation_name":"positively_regulates","term_name":"neuron differentiation","termid":"GO:0030182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of neuron differentiation","synonyms":[{"name":"activation of neuron differentiation","type":"narrow"},{"name":"stimulation of neuron differentiation","type":"narrow"},{"name":"up regulation of neuron differentiation","type":"exact"},{"name":"up-regulation of neuron differentiation","type":"exact"},{"name":"upregulation of neuron differentiation","type":"exact"}],"termid":"GO:0045666"}


id: PBO:0082605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Co-chaperone for Hsp40p; anchored in the ER membrane; with its homolog Ydj1p promotes ER-associated protein degradation (ERAD) of integral membrane substrates; similar to E. coli DnaJ","termid":"PBO:0082605"}


id: PBO:0087258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine/threonine protein kinase; regulates the orientation checkpoint, the morphogenesis checkpoint and the metabolic switch from fermentative to oxidative metabolism by phosphorylating the activation loop of Kin4p, Hsl1p and Snf1p respectively; cooperates with Hsl7p in recruiting Hsl1p to the septin ring, a prerequisite for subsequent recruitment, phosphorylation, and degradation of Swe1p; forms part of the bud neck ring; regulates cytokinesis","termid":"PBO:0087258"}


id: MONDO:0001931
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the tissue surrounding the biliary ducts.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholangitis","termid":"MONDO:0004789"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"pericholangitis","secondary_identifiers":["NCIT:C34916","MEDGEN:18381","SCTID:111373008","UMLS:C0031052","DOID:14272"],"termid":"MONDO:0001931","xrefs":{"Monarch":{"xref_id":"0001931"}}}


id: MONDO:0001707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sarcoidosis affecting the tissues of the heart.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-familial restrictive cardiomyopathy","termid":"MONDO:0016345"},{"relation_name":"is_a","term_name":"sarcoidosis","termid":"MONDO:0019338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiac sarcoidosis","secondary_identifiers":["SCTID:75403004","DOID:13405","NCIT:C35589","MEDGEN:140260","UMLS:C0392077"],"synonyms":[{"name":"heart sarcoidosis","type":"exact"},{"name":"sarcoidosis of heart","type":"exact"}],"termid":"MONDO:0001707","xrefs":{"Monarch":{"xref_id":"0001707"}}}


id: FYPO:0001404
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A colony morphology phenotype in which the outline of a colony growing on a solid surface is not symmetrical.","definition_xrefs":["PomBase:mah","PomBase:mp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal colony morphology","termid":"FYPO:0000150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"irregular colony morphology","synonyms":[{"name":"wavy-edged colony","type":"related"}],"termid":"FYPO:0001404"}


id: PBO:0057334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 521-1","termid":"PBO:0057334"}


id: GO:0180015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of nucleoside from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:21998139","PMID:30658162"],"direct_ancestors":[{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"nucleoside transmembrane transport","termid":"GO:1901642"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"nucleoside import across plasma membrane","termid":"GO:0180015"}


id: GO:0046564
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + oxalate = CO2 + formate.","definition_xrefs":["RHEA:16509","EC:4.1.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"oxalate decarboxylase activity","secondary_identifiers":["KEGG_REACTION:R00522","MetaCyc:OXALATE-DECARBOXYLASE-RXN"],"synonyms":[{"name":"oxalate carboxy-lyase (formate-forming)","type":"related"},{"name":"oxalate carboxy-lyase activity","type":"related"}],"termid":"GO:0046564"}


id: GO:0016578
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histones by removal of ubiquitin groups.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete histone deubiquitination (obsolete GO:0016578)","synonyms":[{"name":"histone deubiquitinylation","type":"exact"},{"name":"histone deubiquitylation","type":"exact"}],"termid":"GO:0016578"}


id: GO:0033192
data:
  {"annotated_genes":["SJAG_03631"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112499],"is_not":false,"summary":null,"term":"GO:0033192"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: protein serine/threonine phosphate + H2O = protein serine/threonine + phosphate, dependent on the presence of calcium-bound calmodulin.","definition_xrefs":["PMID:15359118","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium-dependent protein serine/threonine phosphatase activity","termid":"GO:0004723"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03631":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016788","GO:0140096","GO:0004721","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"calmodulin-dependent protein phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-2730849","Reactome:R-HSA-4551451"],"synonyms":[{"name":"Ca2+/CaM-dependent protein phosphatase activity","type":"related"},{"name":"calcineurin activity","type":"narrow"},{"name":"calcium- and calmodulin-dependent protein phosphatase activity","type":"exact"},{"name":"calcium/calmodulin-dependent protein phosphatase activity","type":"exact"}],"termid":"GO:0033192","terms_by_termid":{"GO:0033192":null}}


id: MONDO:0100478
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brain disorder caused by pathogenic variants in NFIA that is characterized by developmental delay, corpus callosum agenesis/hypoplasia and craniofacial dysmorphism, such as macrocephaly (caused by hydrocephalus or ventriculomegaly), low-set ears, anteverted nostrils and micrognathia. Urinary tract defects (e.g. vesicoureteral reflux, urinary incontinence) are also frequently associated. Other reported variable manifestations include hypotonia, tethered spinal cord, Chiari type I malformation and seizures.","direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain malformations with or without urinary tract defects","secondary_identifiers":["OMIM:613735"],"termid":"MONDO:0100478","xrefs":{"Monarch":{"xref_id":"0100478"}}}


id: GO:0032909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates 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 beta production","termid":"GO:0071634"},{"relation_name":"regulates","term_name":"transforming growth factor beta2 production","termid":"GO:0032906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of transforming growth factor beta2 production","synonyms":[{"name":"regulation of TGF-B2 production","type":"exact"},{"name":"regulation of TGFB2 production","type":"exact"},{"name":"regulation of transforming growth factor-beta2 production","type":"exact"}],"termid":"GO:0032909"}


id: PBO:0058652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6780b","termid":"PBO:0058652"}


id: PBO:0067332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 424, pseudogene","termid":"PBO:0067332"}


id: PBO:0001472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S5 (predicted)","termid":"PBO:0001472"}


id: MOD:01652
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that is produced by formation of an adduct with a sulfonyl halide compound used as a reagent.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfonyl halide reagent derivatized residue","termid":"MOD:01652"}


id: MONDO:0006512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of breast cancer that is estrogen-receptor positive","definition_xrefs":["EFO:1000649"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast carcinoma by gene expression profile","termid":"MONDO:0006116"}],"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":"estrogen-receptor positive breast cancer","secondary_identifiers":["MEDGEN:1843470","DOID:0060075","UMLS:C2938924"],"synonyms":[{"name":"ER+ breast cancer","type":"exact"},{"name":"estrogen receptor positive breast cancer","type":"exact"},{"name":"oestrogen receptor positive breast cancer","type":"exact"}],"termid":"MONDO:0006512","xrefs":{"Monarch":{"xref_id":"0006512"}}}


id: PBO:0076146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate receptor 1","termid":"PBO:0076146"}


id: GO:0061498
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Structure between the central and outer plaques of the mitotic spindle pole body.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate layer of spindle pole body","termid":"GO:0005821"},{"relation_name":"part_of","term_name":"mitotic spindle pole body","termid":"GO:0044732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005816"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005575","GO:0015630","GO:0005816"],"is_obsolete":false,"name":"intermediate layer of mitotic spindle pole body","termid":"GO:0061498"}


id: PBO:0085656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in mitochondrion organization; functions with Nca2p to regulate mitochondrial expression of subunits 6 (Atp6p) and 8 (Atp8p) of the Fo-F1 ATP synthase; SWAT-GFP, seamless-GFP and mCherry fusion proteins localize to the vacuole; member of the SUN family; expression induced in cells treated with the mycotoxin patulin; NCA3 has a paralog, UTH1, that arose from the whole genome duplication","termid":"PBO:0085656"}


id: MONDO:1012425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital merosin-deficient muscular dystrophy, non-human animal","termid":"MONDO:1011802"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital merosin-deficient muscular dystrophy, domestic cat","secondary_identifiers":["OMIA:001619-9685"],"termid":"MONDO:1012425","xrefs":{"Monarch":{"xref_id":"1012425"}}}


id: MONDO:1012371
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dysplasia epiphysealis hememelica, non-human animal","termid":"MONDO:1011769"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dysplasia epiphysealis hememelica, dog","secondary_identifiers":["OMIA:001361-9615"],"termid":"MONDO:1012371","xrefs":{"Monarch":{"xref_id":"1012371"}}}


id: MONDO:0002601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-seminomatous germ cell tumor characterized by the presence of various tissues which correspond to the different germinal layers (endoderm, mesoderm, and ectoderm). It occurs in the testis, ovary, and extragonadal sites including central nervous system, mediastinum, lung, and stomach. According to the level of differentiation of the tissues which comprise the tumor, teratomas are classified as mature or immature. Mature teratomas are composed of well differentiated, adult-type tissues. Immature teratomas are composed of immature, fetal-type tissues. Testicular teratomas in children follow a benign clinical course. Mature ovarian teratomas without a fetal-type component have an excellent outcome. The prognosis of immature ovarian teratomas is related to the grade and stage of the tumor.","definition_xrefs":["NCIT:C3403"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete germ cell and embryonal cancer (obsolete MONDO:0002510)","termid":"MONDO:0002510"},{"relation_name":"is_a","term_name":"nongerminomatous germ cell tumor","termid":"MONDO:0021656"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"teratoma","secondary_identifiers":["DOID:3307","ICDO:9080/1","UMLS:C0039538","MESH:D013724","ONCOTREE:TT","SCTID:36591000119102","MEDGEN:21097"],"synonyms":[{"name":"teratoma","type":"exact"}],"termid":"MONDO:0002601","xrefs":{"Monarch":{"xref_id":"0002601"}}}


id: PBO:0084032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi membrane protein with similarity to mammalian CASP; packaged into COPII vesicles for trafficking between ER and Golgi; genetic interactions with GOS1 (encoding a Golgi snare protein) suggest a role in Golgi function","termid":"PBO:0084032"}


id: GO:0016533
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that has protein serine/threonine kinase activity; in mammals composed of catalytic subunit CDK5 and regulatory subunits CDK5R1 or CDK5R2. Contrary to its gene symbol, CDK5 is not cyclin-dependent.","definition_xrefs":["PMID:15689152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine/threonine protein kinase complex","termid":"GO:1902554"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"protein kinase 5 complex","synonyms":[{"name":"cyclin-dependent protein kinase 5 holoenzyme complex","type":"related"}],"termid":"GO:0016533"}


id: PBO:0017574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ino80 complex HMG box subunit Nht1","termid":"PBO:0017574"}


id: PBO:0047164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 192 member B, pseudogene","termid":"PBO:0047164"}


id: MONDO:0011486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital muscular dystrophy type 1B is a rare, genetic neuromuscular disorder characterized by proximal and symmetrical muscle weakness (particularly of neck, sternomastoid, facial and diaphragm muscles), spinal rigidity, joint contractures (Achilles tendon, elbows, hands), generalized muscle hypertrophy and early respiratory failure (usually in the first decade of life). Patients typically present delayed motor milestones and grossly elevated serum creatine kinase levels, and with disease progression, forced expiratory abdominal squeeze and nocturnal hypoventilation.","definition_xrefs":["Orphanet:98893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"congenital muscular dystrophy 1B","secondary_identifiers":["DOID:0110634","GARD:12586","MEDGEN:346746","OMIM:604801","MESH:C565748","SCTID:764944006","UMLS:C1858118"],"synonyms":[{"name":"CMD1B","type":"exact"},{"name":"MDC1B","type":"exact"},{"name":"congenital muscular dystrophy type 1B","type":"exact"},{"name":"muscular dystrophy, congenital, 1B","type":"related"}],"termid":"MONDO:0011486","xrefs":{"Monarch":{"xref_id":"0011486"}}}


id: GO:1990401
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process occurring during the embryonic phase whose specific outcome is the progression of the lung over time, from its formation to the mature structure.","definition_xrefs":["PMID:24785085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic organ development","termid":"GO:0048568"}],"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":"embryonic lung development","termid":"GO:1990401"}


id: MONDO:0011531
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome","termid":"MONDO:0018997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005267"],"is_obsolete":false,"name":"Noonan syndrome 2","secondary_identifiers":["UMLS:C1854469","GARD:10698","MESH:C548081","NCIT:C176930","DOID:0060580","OMIM:605275","MEDGEN:344290"],"synonyms":[{"name":"NS2","type":"exact"},{"name":"Noonan syndrome 2","type":"exact"},{"name":"Noonan syndrome autosomal recessive","type":"related"},{"name":"Noonan syndrome type 2","type":"exact"},{"name":"Noonan syndrome, autosomal recessive","type":"related"},{"name":"autosomal recessive Noonan syndrome","type":"related"}],"termid":"MONDO:0011531","xrefs":{"Monarch":{"xref_id":"0011531"}}}


id: GO:0010338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to a leaf. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant organ development","termid":"GO:0099402"},{"relation_name":"is_a","term_name":"plant organ formation","termid":"GO:1905393"},{"relation_name":"part_of","term_name":"leaf morphogenesis","termid":"GO:0009965"}],"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":"leaf formation","termid":"GO:0010338"}


id: PBO:0003852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-ATPase assembly factor Pkr1 (predicted)","termid":"PBO:0003852"}


id: PBO:0090778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-O ortholog Mal2","termid":"PBO:0090778"}


id: GO:0045991
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transcription regulation process in which the presence of one carbon source leads to an increase in the frequency, rate, or extent of transcription of specific genes involved in the metabolism of other carbon sources.","definition_xrefs":["PMID:10559153","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA-templated transcription","termid":"GO:0045893"},{"relation_name":"is_a","term_name":"carbon catabolite regulation of transcription","termid":"GO:0045990"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"positively_regulates","termid":"GO:0006351"},{"rel_name":"regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0010467","GO:0006351","GO:0008150","GO:0006355"],"is_obsolete":false,"name":"carbon catabolite activation of transcription","synonyms":[{"name":"positive regulation of transcription by carbon catabolites","type":"exact"}],"termid":"GO:0045991"}


id: GO:0098948
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic specialization membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:mah","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of postsynaptic specialization membrane (obsolete GO:0098948)","synonyms":[{"name":"intrinsic to postsynaptic specialization membrane","type":"narrow"}],"termid":"GO:0098948"}


id: GO:2000306
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of photomorphogenesis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of photomorphogenesis","termid":"GO:0010099"},{"relation_name":"is_a","term_name":"positive regulation of post-embryonic development","termid":"GO:0048582"},{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"positively_regulates","term_name":"photomorphogenesis","termid":"GO:0009640"}],"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 photomorphogenesis","synonyms":[{"name":"positive regulation of plant development in response to light","type":"exact"}],"termid":"GO:2000306"}


id: PBO:0109121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycoside hydrolase family protein Ghs2","termid":"PBO:0109121"}


id: GO:0075108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont stops, prevents, or reduces the frequency, rate or extent of the host adenylate cyclase activity, which catalyze the reaction: ATP = 3',5'-cyclic AMP + diphosphate. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by symbiont of host adenylate cyclase activity (obsolete GO:0075108)","synonyms":[{"name":"Negative regulation by symbiont of host 3',5'-cyclic AMP synthetase activity","type":"exact"},{"name":"Negative regulation by symbiont of host ATP diphosphate-lyase (cyclizing ; 3',5'-cyclic-AMP-forming) activity","type":"exact"},{"name":"Negative regulation by symbiont of host ATP diphosphate-lyase (cyclizing) activity","type":"exact"},{"name":"Negative regulation by symbiont of host ATP pyrophosphate-lyase activity","type":"exact"},{"name":"Negative regulation by symbiont of host adenyl cyclase activity","type":"exact"},{"name":"Negative regulation by symbiont of host adenylyl cyclase activity","type":"exact"},{"name":"Negative regulation by symbiont of host adenylylcyclase activity","type":"exact"},{"name":"Negative regulation by symbiont of host cAMP generating peptide activity","type":"related"}],"termid":"GO:0075108"}


id: PBO:0077204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TM4SF19-DYNLT2B readthrough (NMD candidate)","termid":"PBO:0077204"}


id: MONDO:0014187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial thoracic aortic aneurysm and aortic dissection in which the cause of the disease is a mutation in the PRKG1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial thoracic aortic aneurysm and aortic dissection","termid":"MONDO:0019625"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aortic aneurysm, familial thoracic 8","secondary_identifiers":["OMIM:615436","MEDGEN:815843","UMLS:C3809513","GARD:15966"],"synonyms":[{"name":"AAT8","type":"related"},{"name":"PRKG1 familial thoracic aortic aneurysm and aortic dissection","type":"exact"},{"name":"aortic aneurysm, familial thoracic 8","type":"exact"},{"name":"aortic aneurysm, familial thoracic type 8","type":"exact"},{"name":"familial thoracic aortic aneurysm and aortic dissection caused by mutation in PRKG1","type":"exact"}],"termid":"MONDO:0014187","xrefs":{"Monarch":{"xref_id":"0014187"}}}


id: PBO:0062914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purinergic receptor P2X 6","termid":"PBO:0062914"}


id: MONDO:0018473
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hyperlipoproteinemia (HLP) type 3 is a rare combined hyperlipidemia characterized by high levels of cholesterol and triglycerides, transported by intermediate density lipoproteins (IDLs), and a high risk of premature atherosclerosis and cardiovascular disease.","definition_xrefs":["Orphanet:412"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hyperlipidemia","termid":"MONDO:0001336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"hyperlipoproteinemia type 3","secondary_identifiers":["OMIM:617347","GARD:6703","SCTID:398796005","DOID:3145","UMLS:C0020479","MedDRA:10060751","MEDGEN:9364"],"synonyms":[{"name":"Broad beta disease","type":"related"},{"name":"Broad-betalipoproteinemia","type":"exact"},{"name":"HLP type 3","type":"exact"},{"name":"apolipoprotein E, deficiency or defect of","type":"related"},{"name":"carbohydrate induced hyperlipemia","type":"exact"},{"name":"coronary artery disease, Severe, Susceptibility to","type":"related"},{"name":"dysbetalipoproteinemia","type":"related"},{"name":"dysbetalipoproteinemia due to defect in apolipoprotein E-D","type":"related"},{"name":"dyslipidaemia type 3","type":"exact"},{"name":"dyslipidemia type 3","type":"exact"},{"name":"familial Hyperbeta- and Prebetalipoproteinemia","type":"related"},{"name":"familial dysbetalipoproteinemia","type":"exact"},{"name":"familial hypercholesterolaemia with hyperlipaemia","type":"related"},{"name":"familial hypercholesterolemia with hyperlipemia","type":"related"},{"name":"familial hyperlipoproteinemia type 3","type":"exact"},{"name":"familial type 3 hyperlipoproteinemia","type":"exact"},{"name":"floating-betalipoproteinemia","type":"related"},{"name":"hyperlipemia with Familial Hypercholesterolemic xanthomatosis","type":"related"},{"name":"hyperlipidemia type 3","type":"exact"},{"name":"hyperlipoproteinemia type III","type":"exact"},{"name":"hyperlipoproteinemia, type III","type":"related"},{"name":"low density lipoprotein cholesterol level quantitative trait locus 5","type":"related"},{"name":"remnant disease","type":"exact"},{"name":"remnant hyperlipidemia","type":"exact"},{"name":"remnant removal disease","type":"related"}],"termid":"MONDO:0018473","xrefs":{"Monarch":{"xref_id":"0018473"}}}


id: SO:0001575
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A splice variant that changes the 2 base pair region at the 5' end of an intron.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"splice_site_variant","termid":"SO:0001629"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splice_donor_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":"Jannovar:splice_donor_variant","type":"exact"},{"name":"Seattleseq:splice-donor","type":"exact"},{"name":"VAAST:splice_donor_variant","type":"exact"},{"name":"VEP:splice_donor_variant","type":"exact"},{"name":"snpEff:SPLICE_SITE_DONOR","type":"exact"},{"name":"splice donor variant","type":"exact"}],"termid":"SO:0001575"}


id: PBO:0082581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chorismate mutase; catalyzes the conversion of chorismate to prephenate to initiate the tyrosine/phenylalanine-specific branch of aromatic amino acid biosynthesis","termid":"PBO:0082581"}


id: PBO:0073570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shisa family member 3","termid":"PBO:0073570"}


id: MONDO:0001492
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chronic pulmonary heart disease","termid":"MONDO:0001493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"kyphoscoliotic heart disease","secondary_identifiers":["SCTID:45650007","ICD9:416.1","ICD10CM:I27.1","icd11.foundation:1361660141","MEDGEN:508888","DOID:12325","UMLS:C0152102"],"termid":"MONDO:0001492","xrefs":{"Monarch":{"xref_id":"0001492"}}}


id: PBO:0054490
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 1890","termid":"PBO:0054490"}


id: PBO:0088066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-specific protease; cleaves ubiquitin from ubiquitinated proteins; present in the nucleus and cytoplasm","termid":"PBO:0088066"}


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: FYPO:0002629
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 galactose measured in the cell wall is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance absent from cell during vegetative growth","termid":"FYPO:0001208"},{"relation_name":"is_a","term_name":"decreased level of substance in cell wall during vegetative growth","termid":"FYPO:0002628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002946"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002946","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"galactose absent from cell wall","synonyms":[{"name":"galactose absent from cell surface","type":"related"},{"name":"galactose absent from cell wall during mitotic cell cycle","type":"related"},{"name":"galactose absent from cell wall during vegetative growth","type":"exact"}],"termid":"FYPO:0002629"}


id: PBO:0000461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase D, Pld1","termid":"PBO:0000461"}


id: PBO:0087434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit d of the V0 integral membrane domain of V-ATPase; part of the electrogenic proton pump found in the endomembrane system; required for V1 domain assembly on the vacuolar membrane; the V0 integral membrane domain of vacuolar H+-ATPase (V-ATPase) has five subunits","termid":"PBO:0087434"}


id: PBO:0075461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis associated 12","termid":"PBO:0075461"}


id: GO:0048214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Golgi vesicle fusion to target membrane.","definition_xrefs":["GOC:jid","ISBN:0716731363","PMID:10219233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vesicle fusion","termid":"GO:0031338"},{"relation_name":"regulates","term_name":"Golgi vesicle fusion to target membrane","termid":"GO:0048210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0061024","GO:0016192"],"is_obsolete":false,"name":"regulation of Golgi vesicle fusion to target membrane","termid":"GO:0048214"}


id: GO:0038036
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the sphingolipid sphingosine-1-phosphate (S1P), and transmitting the signal across the membrane by activating an associated G-protein.","definition_xrefs":["GOC:bf","PMID:12728273","Wikipedia:S1PR1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bioactive lipid receptor activity","termid":"GO:0045125"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"sphingosine-1-phosphate receptor activity","synonyms":[{"name":"S1P receptor activity","type":"exact"}],"termid":"GO:0038036"}


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


id: PBO:0058070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4289","termid":"PBO:0058070"}


id: PBO:0075792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine and arginine rich splicing factor 11","termid":"PBO:0075792"}


id: MONDO:0004524
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A thyroid gland adenoma with increased cellularity and nuclear atypia. There is no capsular or vascular invasion. The clinical course is benign.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"follicular thyroid adenoma","termid":"MONDO:0005032"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid gland atypical follicular adenoma","secondary_identifiers":["UMLS:C1266046","DOID:8292","MEDGEN:224756","NCIT:C27729","ICDO:8330/1"],"synonyms":[{"name":"atypical follicular adenoma","type":"exact"},{"name":"atypical follicular adenoma (morphologic abnormality)","type":"exact"},{"name":"thyroid gland atypical follicular adenoma","type":"exact"}],"termid":"MONDO:0004524","xrefs":{"Monarch":{"xref_id":"0004524"}}}


id: MONDO:0020109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete constitutional megaloblastic anemia due to vitamin B12 metabolism disorder (obsolete MONDO:0020109)","secondary_identifiers":["Orphanet:98396"],"termid":"MONDO:0020109","xrefs":{"Monarch":{"xref_id":"0020109"}}}


id: MONDO:0005480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory skin condition caused by direct contact between the skin and either an irritating substance or an allergen.","definition_xrefs":["NCIT:C26743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatitis","termid":"MONDO:0002406"}],"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":"contact dermatitis","secondary_identifiers":["UMLS:C0011616","ICD9:692.89","ICD9:692.9","MEDGEN:8329","SCTID:40275004","MESH:D003877","EFO:0005319","DOID:2773"],"synonyms":[{"name":"contact dermatitis","type":"exact"},{"name":"contact dermatitis/eczema","type":"exact"},{"name":"contact eczema","type":"narrow"},{"name":"dermatitis venenata","type":"exact"},{"name":"dermatitis, venenata","type":"exact"}],"termid":"MONDO:0005480","xrefs":{"Monarch":{"xref_id":"0005480"}}}


id: GO:0019824
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A subform of peroxisome that corresponds to an intermediate in a peroxisome assembly pathway, which operates by conversion of peroxisomal subforms in the direction P1, P2 -> P3 -> P4 -> P5 -> P6. P6 peroxisomes are distinguished from the other subforms on the bases of buoyant density and protein content, and are equivalent to mature peroxisomes.","definition_xrefs":["PMID:10629216"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisome","termid":"GO:0005777"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005777"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005777","GO:0005737"],"is_obsolete":false,"name":"P6 peroxisome","synonyms":[{"name":"peroxisome vesicle","type":"broad"}],"termid":"GO:0019824"}


id: GO:1900867
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving sarcinapterin.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tricarboxylic acid metabolic process","termid":"GO:0072350"},{"relation_name":"is_a","term_name":"methanopterin-containing compound metabolic process","termid":"GO:2001115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"sarcinapterin metabolic process","synonyms":[{"name":"sarcinapterin metabolism","type":"exact"}],"termid":"GO:1900867"}


id: PBO:0045750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Epstein Barr virus modification site 1","termid":"PBO:0045750"}


id: GO:1901691
data:
  {"annotated_genes":["SJAG_01669","SJAG_01129"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[86918,86919],"is_not":false,"summary":null,"term":"GO:1901691"}]},"cv_name":"molecular_function","definition":"Binding to proton.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01129":null,"SJAG_01669":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":"proton binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"hydrogen ion binding","type":"exact"}],"termid":"GO:1901691","terms_by_termid":{"GO:1901691":null}}


id: GO:0042159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of any conjugated, water-soluble protein in which the covalently attached nonprotein group consists of a lipid or lipids.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein catabolic process","termid":"GO:0030163"},{"relation_name":"is_a","term_name":"lipoprotein metabolic process","termid":"GO:0042157"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0030163"],"is_obsolete":false,"name":"lipoprotein catabolic process","synonyms":[{"name":"lipoprotein breakdown","type":"exact"},{"name":"lipoprotein catabolism","type":"exact"},{"name":"lipoprotein degradation","type":"exact"}],"termid":"GO:0042159"}


id: FYPO:0006845
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of H3-K9 specific histone methyltransferase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"},{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000257","FYPO:0000652","FYPO:0000002"],"is_obsolete":false,"name":"normal histone methyltransferase activity (H3-K9 specific) activity","synonyms":[{"name":"normal H3-K9 specific histone methyltransferase activity","type":"exact"}],"termid":"FYPO:0006845"}


id: PBO:0081939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger HIT-type containing 2","termid":"PBO:0081939"}


id: GO:0035032
data:
  {"annotated_genes":["SJAG_02699","SJAG_00114","SJAG_04552","SJAG_04860","SJAG_03403","SJAG_01876"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[110660,96779,93823,91824,101310],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034271"},{"annotations":[91825,101311,96780,104871],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034272"}]},"cv_name":"cellular_component","definition":"A phosphatidylinositol 3-kinase complex that contains a catalytic class III phosphoinositide 3-kinase (PI3K) subunit bound to a regulatory (adaptor) subunit. Additional adaptor proteins may be present. Class III PI3Ks have a substrate specificity restricted to phosphatidylinositol (PI).","definition_xrefs":["PMID:9255069","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol 3-kinase complex","termid":"GO:0005942"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_01876":null,"SJAG_02699":null,"SJAG_03403":null,"SJAG_04552":null,"SJAG_04860":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"phosphatidylinositol 3-kinase complex, class III","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"class III PI3K complex","type":"exact"},{"name":"phosphoinositide 3-kinase complex, class III","type":"exact"}],"termid":"GO:0035032","terms_by_termid":{"GO:0034271":null,"GO:0034272":null}}


id: PBO:0053103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"late cornified envelope pseudogene 2","termid":"PBO:0053103"}


id: PBO:0059050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloid cell nuclear differentiation antigen","termid":"PBO:0059050"}


id: GO:0060875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progession of the lateral semicircular canal from its initial formation to the mature structure.","definition_xrefs":["GOC:sdb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"semicircular canal development","termid":"GO:0060872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral semicircular canal development","termid":"GO:0060875"}


id: PBO:0055608
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 3047","termid":"PBO:0055608"}


id: GO:1903577
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 L-arginine stimulus.","definition_xrefs":["GO_REF:0000071","PMID:6394628","GOC:mr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amino acid stimulus","termid":"GO:0071230"},{"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 L-arginine","termid":"GO:1903576"}],"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 L-arginine","termid":"GO:1903577"}


id: FYPO:0003080
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which genetic imprinting at the mating-type locus does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal genetic imprinting at mating-type locus","termid":"FYPO:0003079"},{"relation_name":"is_a","term_name":"abolished biological process","termid":"FYPO:0005448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abolished genetic imprinting at mating-type locus","synonyms":[{"name":"abolished genetic imprinting at mating-type locus during mitotic cell cycle","type":"related"},{"name":"genetic imprinting at mating-type locus abolished","type":"exact"},{"name":"genetic imprinting at mating-type locus abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0003080"}


id: MONDO:0012945
data:
  {"annotated_genes":["SJAG_02289"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86002],"is_not":false,"summary":null,"term":"MONDO:0012945"}]},"cv_name":"mondo","definition":"Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the FIG4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"amyotrophic lateral sclerosis type 11","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C567244","OMIM:612577","UMLS:C2675491","DOID:0060202","GARD:10496","MEDGEN:393399"],"synonyms":[{"name":"ALS11","type":"exact"},{"name":"FIG4 amyotrophic lateral sclerosis","type":"exact"},{"name":"amyotrophic lateral sclerosis 11","type":"exact"},{"name":"amyotrophic lateral sclerosis caused by mutation in FIG4","type":"exact"},{"name":"amyotrophic lateral sclerosis type 11","type":"exact"}],"termid":"MONDO:0012945","terms_by_termid":{"MONDO:0012945":null},"xrefs":{"Monarch":{"xref_id":"0012945"}}}


id: PBO:0110044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THAP3 pseudogene 1","termid":"PBO:0110044"}


id: GO:0106167
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by the detection of extracellular ATP.","definition_xrefs":["PMID:20817461","GOC:tb","PMID:29274390","PMID:12948585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signal transduction","termid":"GO:0007165"},{"relation_name":"is_a","term_name":"cellular response to ATP","termid":"GO:0071318"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"extracellular ATP signaling","termid":"GO:0106167"}


id: GO:0002516
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The apoptotic death of B cells which is part of B cell tolerance induction.","definition_xrefs":["GOC:add","ISBN:0781735149","GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell apoptotic process","termid":"GO:0001783"},{"relation_name":"is_a","term_name":"apoptotic process involved in development","termid":"GO:1902742"},{"relation_name":"part_of","term_name":"B cell tolerance induction","termid":"GO:0002514"}],"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":"B cell deletion","synonyms":[{"name":"B lymphocyte deletion","type":"exact"},{"name":"B-cell deletion","type":"exact"},{"name":"B-lymphocyte deletion","type":"exact"}],"termid":"GO:0002516"}


id: PATO:0002286
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Branchiness quality inhering in a bearer by virtue of decreasing the degree to which there are subdivisions or offshoots in a bearer entity.","definition_xrefs":["PATOC:CVS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branched","termid":"PATO:0000402"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased branchiness","termid":"PATO:0002286"}


id: PR:P24487
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP synthase subunit alpha, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase subunit alpha, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC14C4.14","secondary_identifiers":["UniProtKB:P24487"],"synonyms":[{"name":"Spom972h-ATP5A1","type":"exact"}],"termid":"PR:P24487"}


id: PBO:0086778
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; SWAT-GFP and mCherry fusion proteins localize to the endoplasmic reticulum; YDL241W is not an essential gene","termid":"PBO:0086778"}


id: MONDO:0000069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete multiple endocrine neoplasia (obsolete MONDO:0000069)","termid":"MONDO:0000069","xrefs":{"Monarch":{"xref_id":"0000069"}}}


id: PBO:0034070
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-before_or_simultaneous_with","termid":"PBO:0034070"}


id: GO:0050389
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucurono-6,2-lactone + H2O = D-glucuronate.","definition_xrefs":["EC:3.1.1.19","MetaCyc:URONOLACTONASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0016788","GO:0003674"],"is_obsolete":false,"name":"uronolactonase activity","secondary_identifiers":["RHEA:13337"],"synonyms":[{"name":"D-glucurono-6,2-lactone lactonohydrolase activity","type":"related"},{"name":"glucuronolactonase activity","type":"related"}],"termid":"GO:0050389"}


id: MONDO:0003186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infrequent esophageal carcinoma arising from esophageal glands. (WHO)","definition_xrefs":["NCIT:C5342"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenoid cystic carcinoma","termid":"MONDO:0004971"},{"relation_name":"is_a","term_name":"esophageal adenocarcinoma","termid":"MONDO:0005028"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"esophageal adenoid cystic carcinoma","secondary_identifiers":["MEDGEN:232468","DOID:4878","UMLS:C1333441"],"synonyms":[{"name":"adenoid cystic carcinoma of esophagus","type":"exact"},{"name":"adenoid cystic carcinoma of oesophagus","type":"exact"},{"name":"adenoid cystic carcinoma of the esophagus","type":"exact"},{"name":"adenoid cystic carcinoma of the oesophagus","type":"exact"},{"name":"adenoid cystic carcinoma, esophagus","type":"exact"},{"name":"adenoid cystic carcinoma, oesophagus","type":"exact"},{"name":"adenoid cystic esophagus carcinoma","type":"exact"},{"name":"adenoid cystic oesophagus carcinoma","type":"exact"},{"name":"esophageal adenoid cystic cancer","type":"exact"},{"name":"esophageal adenoid cystic carcinoma","type":"exact"},{"name":"esophagus adenoid cystic carcinoma","type":"exact"},{"name":"oesophagus adenoid cystic carcinoma","type":"exact"}],"termid":"MONDO:0003186","xrefs":{"Monarch":{"xref_id":"0003186"}}}


id: PR:Q9USU7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hmo1 gene.","definition_xrefs":["UniProtKB:Q9USU7","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":"HMG box-containing protein C28F2.11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC28F2.11","synonyms":[{"name":"Spom972h-hmo1","type":"exact"}],"termid":"PR:Q9USU7"}


id: PBO:0036101
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_binucleate_aseptate_cell_with_mitotic_cell_cycle_arrest_before_cell_separation","termid":"PBO:0036101"}


id: MONDO:0010096
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":"tardive dyskinesia","secondary_identifiers":["SCTID:102449007","MEDGEN:151939","MESH:D000071057","OMIM:272620","UMLS:C0686347","HP:0040141"],"synonyms":[{"name":"tardive dyskinesia","type":"exact"},{"name":"tardive dyskinesia (disease)","type":"exact"}],"termid":"MONDO:0010096","xrefs":{"Monarch":{"xref_id":"0010096"}}}


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:0052636
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of an arabinosyl group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"arabinosyltransferase activity","synonyms":[{"name":"arabinosyl transferase activity","type":"exact"}],"termid":"GO:0052636"}


id: MONDO:0005030
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A fetus that does not grow beyond the 10th percentile of conventionally accepted weight for gestational age.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"placenta disorder","termid":"MONDO:0005917"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fetal growth restriction","secondary_identifiers":["ICD9:764.91","UMLS:C0015934","ICD9:764.97","NCIT:C114875","ICD9:764.94","MEDGEN:4693","ICD9:764.92","ICD9:764.95","ICD9:764.96","ICD9:764.99","MESH:D005317","ICD9:764.98","SCTID:22033007","EFO:0000495","ICD9:764.93","ICD9:764.90","ICD9:764.9"],"synonyms":[{"name":"IUGR","type":"exact"},{"name":"fetal Growth retardation","type":"exact"},{"name":"fetal SGA","type":"exact"},{"name":"fetal growth retardation","type":"exact"},{"name":"fetal small for gestational Age","type":"exact"},{"name":"fetus small for gestational Age","type":"exact"},{"name":"foetal Growth retardation","type":"exact"},{"name":"foetal SGA","type":"exact"},{"name":"foetal growth retardation","type":"exact"},{"name":"foetal small for gestational Age","type":"exact"},{"name":"foetus small for gestational Age","type":"exact"},{"name":"intrauterine Growth restriction","type":"exact"},{"name":"intrauterine Growth retardation","type":"exact"}],"termid":"MONDO:0005030","xrefs":{"Monarch":{"xref_id":"0005030"}}}


id: MONDO:0014329
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any atrial standstill in which the cause of the disease is a mutation in the NPPA gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrial standstill","termid":"MONDO:0015281"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"atrial standstill 2","secondary_identifiers":["OMIM:615745","UMLS:C3810401","DOID:0080663","GARD:18612","MEDGEN:816731"],"synonyms":[{"name":"ATRST2","type":"related"},{"name":"NPPA atrial standstill","type":"exact"},{"name":"atrial dilation and standstill","type":"related"},{"name":"atrial standstill 2","type":"exact"},{"name":"atrial standstill caused by mutation in NPPA","type":"exact"},{"name":"atrial standstill type 2","type":"exact"},{"name":"cardiomyopathy, atrial dilated, with atrial standstill","type":"related"}],"termid":"MONDO:0014329","xrefs":{"Monarch":{"xref_id":"0014329"}}}


id: PBO:0084081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP/GDP exchange factor for Rsr1p (Bud1p); required for both axial and bipolar budding patterns; mutants exhibit random budding in all cell types","termid":"PBO:0084081"}


id: FYPO:0003318
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell adhesion phenotype observed in the vegetative growth phase of the life cycle in which galactose-specific flocculation does not occur. Galactose-specific flocculation is the non-sexual aggregation of cells, mediated via the binding of cell wall proteins on one cell to galactose residues on the other.","definition_xrefs":["PomBase:mah","GO:0036349"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished galactose-specific flocculation","termid":"FYPO:0005504"},{"relation_name":"is_a","term_name":"abolished flocculation during vegetative growth","termid":"FYPO:0009112"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished galactose-specific flocculation during vegetative growth","synonyms":[{"name":"abolished cell-cell adhesion involved in galactose-specific flocculation during vegetative growth","type":"exact"},{"name":"abolished galactose-specific flocculation during mitotic cell cycle","type":"related"},{"name":"galactose-specific flocculation abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0003318"}


id: PBO:0087938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translational repressor;  involved in polar growth, wall integrity, autodiploidization; regulated by Cbk1p phosphorylation to affect bud-specific translational control and localization of specific mRNAs; binds 5'UTRs of mRNAs encoding cell wall proteins; recognizes CNYTCNYT motif in RNA; interacts with TOR pathway components; nucleocytoplasmic shuttling appears to be critical to Ssd1p function; W303 lacks a functional SSD1 gene product; pseudonuclease descended from Dis3L2-family nucleases","termid":"PBO:0087938"}


id: PBO:0084966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetyltransferase; confers resistance to the sphingolipid biosynthesis inhibitor myriocin (ISP-1) by converting it into N-acetyl-myriocin, co-operates with Ypk1p in mediating resistance to myriocin","termid":"PBO:0084966"}


id: PBO:0066967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 269","termid":"PBO:0066967"}


id: GO:0014722
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of skeletal muscle contraction by changing the calcium ion signals that trigger contraction.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of skeletal muscle contraction","termid":"GO:0014819"},{"relation_name":"is_a","term_name":"calcium-mediated signaling","termid":"GO:0019722"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of skeletal muscle contraction by calcium ion signaling","synonyms":[{"name":"regulation of skeletal muscle contraction by calcium ion signalling","type":"exact"}],"termid":"GO:0014722"}


id: PBO:0064034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 68","termid":"PBO:0064034"}


id: MONDO:1011073
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis that occurs in Francois's langur.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urolithiasis, Francois's langur","secondary_identifiers":["OMIA:001033-54180"],"termid":"MONDO:1011073","xrefs":{"Monarch":{"xref_id":"1011073"}}}


id: MONDO:0006399
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rhabdoid tumor of the kidney (obsolete MONDO:0006399)","termid":"MONDO:0006399","xrefs":{"Monarch":{"xref_id":"0006399"}}}


id: PBO:0029926
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_GMP_binding","termid":"PBO:0029926"}


id: GO:0103044
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-glutamate + ATP + a [protein] C-terminal L-glutamate = ADP + hydrogenphosphate + H+ + a [protein] with C-terminal alpha-L-glutamate-alpha-L-glutamate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete ribosomal protein S6 glutamate-glutamate ligase activity (obsolete GO:0103044)","termid":"GO:0103044"}


id: MONDO:0005511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Deficiency of janus kinase-3 causing the near absence of T lymphocytes and Natural killer cells; and normal or elevated B lymphocytes due to an autosomal recessive variant of severe combined immunodeficiency.","definition_xrefs":["EFO:0005565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"severe combined immunodeficiency","termid":"MONDO:0015974"}],"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":"janus kinase-3 deficiency","secondary_identifiers":["Wikipedia:Janus_kinase_3_deficiency","DOID:0060008"],"termid":"MONDO:0005511","xrefs":{"Monarch":{"xref_id":"0005511"}}}


id: PATO:0002525
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer being in a position that produces a separation in, or acting to separate, another entity.","definition_xrefs":["PATOC:EJS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"separating","termid":"PATO:0002525"}


id: MONDO:0030317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiomyopathy, familial hypertrophic, 28","secondary_identifiers":["UMLS:C5543616","MEDGEN:1779612","OMIM:619402"],"synonyms":[{"name":"CMH28","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 28","type":"exact"}],"termid":"MONDO:0030317","xrefs":{"Monarch":{"xref_id":"0030317"}}}


id: PBO:0039079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-acylglycerol-3-phosphate O-acyltransferase 5 pseudogene 1","termid":"PBO:0039079"}


id: PBO:0087439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit F of the V1 peripheral membrane domain of V-ATPase; part of the electrogenic proton pump found throughout the endomembrane system; required for the V1 domain to assemble onto the vacuolar membrane; the V1 peripheral membrane domain of vacuolar H+-ATPase (V-ATPase) has eight subunits","termid":"PBO:0087439"}


id: PBO:0044001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CUB and Sushi multiple domains 1","termid":"PBO:0044001"}


id: MONDO:0004908
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete galactosemia (obsolete MONDO:0004908)","termid":"MONDO:0004908","xrefs":{"Monarch":{"xref_id":"0004908"}}}


id: GO:0018661
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + NADH + O2 + orcinol = 2,3,5-trihydroxytoluene + H2O + NAD+.","definition_xrefs":["EC:1.14.13.6","RHEA:19601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"orcinol 2-monooxygenase activity","secondary_identifiers":["UM-BBD_reactionID:r0092","MetaCyc:ORCINOL-2-MONOOXYGENASE-RXN","KEGG_REACTION:R02830"],"synonyms":[{"name":"orcinol hydroxylase activity","type":"exact"},{"name":"orcinol,NADH:oxygen oxidoreductase (2-hydroxylating)","type":"related"}],"termid":"GO:0018661"}


id: PBO:0082589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cis-Golgi localized monothiol glutaredoxin, binds Fe-S cluster; more similar in activity to dithiol than other monothiol glutaredoxins; involved in the oxidative stress response; GRX6 has a paralog, GRX7, that arose from the whole genome duplication","termid":"PBO:0082589"}


id: GO:0060518
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of epithelial cells from one site to another contributing to the elongation of the primary prostatic bud.","definition_xrefs":["GOC:dph","PMID:18977204"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell migration","termid":"GO:0010631"},{"relation_name":"part_of","term_name":"primary prostatic bud elongation","termid":"GO:0060516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell migration involved in prostatic bud elongation","termid":"GO:0060518"}


id: PR:O74492
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 5-hydroxyisourate hydrolase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04832","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":"5-hydroxyisourate hydrolase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC285.04","secondary_identifiers":["UniProtKB:O74492"],"synonyms":[{"name":"HIU hydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"HIUHase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-Urah","type":"exact"},{"name":"transthyretin-like protein C285.04 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74492"}


id: MOD:01769
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to O-palmitoleyl-L-threonine.","definition_xrefs":["OMSSA:188","PubMed:6642431","Unimod:431#T","RESID:AA0079#var","PubMed:8413602"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-palmitoleylated residue","termid":"MOD:01768"},{"relation_name":"is_a","term_name":"O3-acylated L-threonine","termid":"MOD:02004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"O-palmitoleyl-L-threonine","synonyms":[{"name":"(2S,3R)-2-amino-3-((Z)-9-hexadecenoyloxy)butanoic acid","type":"exact"},{"name":"L-threonine cis-9-hexadecenoate ester","type":"exact"},{"name":"O-palmitoleylated L-threonine","type":"exact"},{"name":"O3-palmitoleyl-threonine","type":"exact"},{"name":"Palmitoleyl","type":"related"},{"name":"mod188","type":"exact"},{"name":"palmitoleyl","type":"related"}],"termid":"MOD:01769"}


id: GO:0031499
data:
  {"annotated_genes":["SJAG_16455","SJAG_01176","SJAG_03984"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87582,98805,112394],"is_not":false,"summary":null,"term":"GO:0031499"}]},"cv_name":"cellular_component","definition":"A multiprotein complex having distributive polyadenylation activity of a variety of RNA substrates including hypomodified and incorrectly folded tRNAs, pre-snRNAs, pre-snoRNAs, incorrectly spliced or processed pre-mRNAs, cryptic unstable transcripts (CUTs), pre-rRNAs and rRNA fragments released as part of rRNA processing. In S. cerevisiae, the complex consists of either Pap2 (also known as Trf4) or Trf5, Air1 or Air2, and Mtr4, and is involved in RNA 3'-end processing and in RNA surveillance and quality control.","definition_xrefs":["PMID:16973437","PMID:16374505","PMID:16431988","PMID:15828860","PMID:15935759","PMID:16373491","PMID:15173578","PMID:17410208","PMID:17652137","PMID:15935758"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01176":null,"SJAG_03984":null,"SJAG_16455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"TRAMP complex","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:TRAMP_complex"],"synonyms":[{"name":"TRAMP4 complex","type":"narrow"},{"name":"TRAMP5 complex","type":"narrow"},{"name":"Trf4 complex","type":"narrow"},{"name":"Trf4 poly(A) polymerase complex","type":"narrow"},{"name":"Trf4p-Air2p-Mtr4p polyadenylation complex","type":"narrow"}],"termid":"GO:0031499","terms_by_termid":{"GO:0031499":null}}


id: MONDO:0010088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple sulfatase deficiency (MSD) is a very rare and fatal lysosomal storage disease characterized by a clinical phenotype that combines the features of different sulfatase deficiencies (whether lysosomal or not) that can have neonatal (most severe), infantile (most common) and juvenile (rare) presentations with manifestations including hypotonia, coarse facial features, mild deafness, skeletal anomalies, ichthyosis, hepatomegaly, developmental delay, progressive neurologic deterioration and hydrocephalus.","definition_xrefs":["Orphanet:585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"sphingolipidosis","termid":"MONDO:0019255"},{"relation_name":"is_a","term_name":"lysosomal storage disease with skeletal involvement","termid":"MONDO:0800088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525","MONDO:0002561"],"is_obsolete":false,"name":"mucosulfatidosis","secondary_identifiers":["NCIT:C84908","OMIM:272200","NORD:1471","GARD:5061","NANDO:2200566","DOID:0050441","MESH:D052517","UMLS:C0268263","MEDGEN:75664","NANDO:1200083","icd11.foundation:848083807","SCTID:54898003","NANDO:1200624"],"synonyms":[{"name":"MSD","type":"exact"},{"name":"Multiple Sulfatase Deficiency","type":"exact"},{"name":"juvenile sulfatidosis","type":"related"},{"name":"juvenile sulfatidosis, Austin type","type":"exact"},{"name":"mucosulfatidosis","type":"exact"},{"name":"multiple sulfatase deficiency","type":"related"},{"name":"multiple sulfatase deficiency disease","type":"exact"},{"name":"sulfatidosis juvenile, Austin type","type":"related"},{"name":"sulfatidosis, juvenile, Austin type","type":"exact"}],"termid":"MONDO:0010088","xrefs":{"Monarch":{"xref_id":"0010088"}}}


id: MONDO:0003685
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor that involves the retroperitoneal space.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"retroperitoneal cancer","termid":"MONDO:0005941"},{"relation_name":"is_a","term_name":"germ cell tumor","termid":"MONDO:0005040"},{"relation_name":"is_a","term_name":"retroperitoneal neoplasm","termid":"MONDO:0024645"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retroperitoneal germ cell neoplasm","secondary_identifiers":["NCIT:C6447","MEDGEN:233406","UMLS:C1335776","DOID:5874"],"synonyms":[{"name":"germ cell neoplasm of retroperitoneum","type":"exact"},{"name":"germ cell neoplasm of the retroperitoneum","type":"exact"},{"name":"germ cell tumor of retroperitoneum","type":"exact"},{"name":"germ cell tumor of the retroperitoneum","type":"exact"},{"name":"germ cell tumour of retroperitoneum","type":"exact"},{"name":"germ cell tumour of the retroperitoneum","type":"exact"},{"name":"retroperitoneal germ cell tumor","type":"exact"},{"name":"retroperitoneal germ cell tumour","type":"exact"}],"termid":"MONDO:0003685","xrefs":{"Monarch":{"xref_id":"0003685"}}}


id: PBO:0036077
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-stubby_vegetative_cell","termid":"PBO:0036077"}


id: FYPO:0002592
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone phosphorylation does not occur. All histone phosphorylation may be affected, or phosphorylation of specific sites on specific histones may be abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein modification during vegetative growth","termid":"FYPO:0000544"},{"relation_name":"is_a","term_name":"abnormal histone phosphorylation during vegetative growth","termid":"FYPO:0002591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002274","FYPO:0002494","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished histone phosphorylation during vegetative growth","synonyms":[{"name":"abolished histone phosphorylation during mitotic cell cycle","type":"related"},{"name":"histone phosphorylation abolished during vegetative growth","type":"exact"},{"name":"histone phosphorylation absent during vegetative growth","type":"exact"}],"termid":"FYPO:0002592"}


id: PBO:0091499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PI31 proteasome inhibitor Fub1","termid":"PBO:0091499"}


id: GO:0033409
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a UAU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0060090","GO:0003674","GO:0005488","GO:0003723"],"is_obsolete":false,"name":"UAU codon-amino acid adaptor activity","synonyms":[{"name":"TAT codon-amino acid adaptor activity","type":"exact"},{"name":"tyrosine tRNA","type":"related"}],"termid":"GO:0033409"}


id: PBO:0080811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-ray repair cross complementing 6 pseudogene 1","termid":"PBO:0080811"}


id: PBO:0039706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloid beta precursor like protein 1","termid":"PBO:0039706"}


id: GO:2000579
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of ATP-dependent microtubule motor activity, minus-end-directed.","definition_xrefs":["GOC:kmv","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of microtubule motor activity, minus-end-directed (obsolete GO:2000579)","synonyms":[{"name":"positive regulation of ATP-dependent microtubule motor activity, minus-end-directed","type":"exact"},{"name":"positive regulation of kinesin ATP phosphohydrolase (minus-end-directed)","type":"exact"},{"name":"positive regulation of minus-end-directed kinesin ATPase activity","type":"exact"},{"name":"positive regulation of minus-end-directed microtubule motor activity","type":"broad"}],"termid":"GO:2000579"}


