# terms

id: MONDO:0006515
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute inflammatory process that leads to necrosis of the pancreatic parenchyma. Signs and symptoms include severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock. Causes include alcohol consumption, presence of gallstones, trauma, and drugs.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatitis","termid":"MONDO:0004982"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"acute pancreatitis","secondary_identifiers":["ICD9:577.0","NCIT:C95437","MEDGEN:7872","DOID:2913","icd11.foundation:698285441","UMLS:C0001339","Wikipedia:Acute_pancreatitis","HP:0001735","SCTID:7881005","EFO:1000652"],"synonyms":[{"name":"acute pancreatitis (disorder) [ambiguous]","type":"exact"},{"name":"pancreatitis, acute","type":"exact"}],"termid":"MONDO:0006515","xrefs":{"Monarch":{"xref_id":"0006515"}}}


id: MONDO:0009430
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive hypophosphatemic rickets in which the cause of the disease is a mutation in the DMP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive hypophosphatemic rickets","termid":"MONDO:0017324"},{"relation_name":"is_a","term_name":"abnormal mineralization disorder","termid":"MONDO:0800096"}],"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":"hypophosphatemic rickets, autosomal recessive, 1","secondary_identifiers":["OMIM:241520","GARD:18416","MEDGEN:1632314","UMLS:C4551495","MESH:C562792"],"synonyms":[{"name":"ARHR1","type":"related"},{"name":"Arhr","type":"related"},{"name":"DMP1 autosomal recessive hypophosphatemic rickets","type":"exact"},{"name":"autosomal recessive hypophosphatemic rickets caused by mutation in DMP1","type":"exact"},{"name":"hypophosphatemia, autosomal recessive","type":"related"},{"name":"hypophosphatemic rickets, AR","type":"exact"},{"name":"hypophosphatemic rickets, autosomal recessive, 1","type":"exact"},{"name":"hypophosphatemic rickets, autosomal recessive, type 1","type":"exact"}],"termid":"MONDO:0009430","xrefs":{"Monarch":{"xref_id":"0009430"}}}


id: PBO:0040833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"baculoviral IAP repeat containing 7","termid":"PBO:0040833"}


id: GO:2000237
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of tRNA processing.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of gene expression","termid":"GO:0010628"},{"relation_name":"is_a","term_name":"positive regulation of tRNA metabolic process","termid":"GO:1903328"},{"relation_name":"is_a","term_name":"regulation of tRNA processing","termid":"GO:2000235"},{"relation_name":"positively_regulates","term_name":"tRNA processing","termid":"GO:0008033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0006399","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of tRNA processing","synonyms":[{"name":"positive regulation of tRNA maturation","type":"exact"}],"termid":"GO:2000237"}


id: PBO:0077720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNPO3 pseudogene 1","termid":"PBO:0077720"}


id: FYPO:0002255
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the nucleus is larger than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear morphology","termid":"FYPO:0002256"}],"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:0002403"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002403","FYPO:0000002"],"is_obsolete":false,"name":"enlarged nucleus","synonyms":[{"name":"enlarged nuclei","type":"exact"}],"termid":"FYPO:0002255"}


id: PBO:0051930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inter-alpha-trypsin inhibitor heavy chain 2","termid":"PBO:0051930"}


id: GO:0035103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The proteolytic release of a transcriptionally active sterol regulatory element binding protein (SREBP) from intracellular membranes, freeing it to move to the nucleus to upregulate transcription of target genes, in response to altered levels of one or more lipids.","definition_xrefs":["GOC:bf","GOC:vw","PMID:12923525"],"gene_count":0,"genotype_count":0,"name":"obsolete sterol regulatory element binding protein cleavage (obsolete GO:0035103)","synonyms":[{"name":"SREBP cleavage","type":"exact"},{"name":"sterol depletion response, SREBP cleavage","type":"exact"},{"name":"sterol regulatory element binding protein cleavage involved in ER-nuclear sterol response pathway","type":"narrow"}],"termid":"GO:0035103"}


id: PBO:0063639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"profilin 5, pseudogene","termid":"PBO:0063639"}


id: FYPO:0002628
data:
  {"alleles_by_uniquename":{"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119003],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003727"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of a specific substance measured in the cell wall is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"},{"relation_name":"is_a","term_name":"altered level of substance in cell wall during vegetative growth","termid":"FYPO:0002627"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04697":null},"genotype_count":1,"genotypes_by_uniquename":{"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002946"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002946","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased level of substance in cell wall during vegetative growth","references_by_uniquename":{"PMID:36058798":null},"single_locus_annotated_genes":["SJAG_04697"],"single_locus_genotype_uniquenames":["gms1delta"],"synonyms":[{"name":"decreased level of substance in cell wall during mitotic cell cycle","type":"related"},{"name":"reduced level of substance in cell wall during vegetative growth","type":"exact"}],"termid":"FYPO:0002628","terms_by_termid":{"FYPO:0003727":null,"FYPO_EXT:0000001":null}}


id: GO:0052455
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The alteration by an organism of the levels of jasmonic acid in the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of jasmonic acid levels in symbiont (obsolete GO:0052455)","synonyms":[{"name":"modulation by organism of jasmonic acid levels in symbiont","type":"exact"}],"termid":"GO:0052455"}


id: GO:0050210
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dimethylallyl diphosphate + H2O = diphosphate + prenol.","definition_xrefs":["RHEA:21496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diphosphoric monoester hydrolase activity","termid":"GO:0016794"}],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"prenyl-diphosphatase activity","secondary_identifiers":["EC:3.1.7.1","MetaCyc:PRENYL-PYROPHOSPHATASE-RXN"],"synonyms":[{"name":"prenol pyrophosphatase activity","type":"related"},{"name":"prenyl-diphosphate diphosphohydrolase activity","type":"related"},{"name":"prenyl-pyrophosphatase activity","type":"exact"},{"name":"prenylphosphatase activity","type":"related"}],"termid":"GO:0050210"}


id: PBO:0042903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cofilin 1","termid":"PBO:0042903"}


id: GO:0005124
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to scavenger receptors, a family of proteins that are expressed on myeloid cells and are involved in the uptake of effete cellular components and foreign particles.","definition_xrefs":["GOC:ceb"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"scavenger receptor binding","synonyms":[{"name":"scavenger receptor ligand","type":"narrow"}],"termid":"GO:0005124"}


id: PR:O94410
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug163 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 163 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.03","synonyms":[{"name":"Spom972h-mug163","type":"exact"}],"termid":"PR:O94410"}


id: MONDO:0021459
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the esophagus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign digestive system neoplasm","termid":"MONDO:0000385"},{"relation_name":"is_a","term_name":"thoracic benign neoplasm","termid":"MONDO:0000634"},{"relation_name":"is_a","term_name":"neoplasm of esophagus","termid":"MONDO:0021355"}],"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":"benign neoplasm of esophagus","secondary_identifiers":["SCTID:92091003","ICD10CM:D13.0","UMLS:C0153942","ICD9:211.0","MEDGEN:102297","NCIT:C3598"],"synonyms":[{"name":"benign esophageal neoplasm","type":"exact"},{"name":"benign esophageal tumor","type":"exact"},{"name":"benign esophageal tumour","type":"exact"},{"name":"benign esophagus neoplasm","type":"exact"},{"name":"benign esophagus tumor","type":"exact"},{"name":"benign neoplasm of the esophagus","type":"exact"},{"name":"benign neoplasm of the oesophagus","type":"exact"},{"name":"benign oesophagus neoplasm","type":"exact"},{"name":"benign oesophagus tumour","type":"exact"},{"name":"benign tumor of esophagus","type":"exact"},{"name":"benign tumor of the esophagus","type":"exact"},{"name":"benign tumour of oesophagus","type":"exact"},{"name":"benign tumour of the oesophagus","type":"exact"},{"name":"esophagus benign neoplasm","type":"exact"},{"name":"oesophagus benign neoplasm","type":"exact"}],"termid":"MONDO:0021459","xrefs":{"Monarch":{"xref_id":"0021459"}}}


id: GO:0062013
data:
  {"annotated_genes":["SJAG_04018","SJAG_02406","SJAG_03538","SJAG_01672","SJAG_00685","SJAG_05006"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070452"},{"annotations":[96079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001172"},{"annotations":[89204],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905857"},{"annotations":[113123,88551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090180"},{"annotations":[88703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904775"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of a small molecule metabolic process.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of metabolic process","termid":"GO:0009893"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"positively_regulates","term_name":"small molecule metabolic process","termid":"GO:0044281"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_01672":null,"SJAG_02406":null,"SJAG_03538":null,"SJAG_04018":null,"SJAG_05006":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"positive regulation of small molecule metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"positive regulation of small molecule metabolism","type":"exact"}],"termid":"GO:0062013","terms_by_termid":{"GO:0070452":null,"GO:0090180":null,"GO:1904775":null,"GO:1905857":null,"GO:2001172":null}}


id: PBO:0058266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4644","termid":"PBO:0058266"}


id: PBO:0070879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15 pseudogene 11","termid":"PBO:0070879"}


id: MONDO:0018603
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary pulmonary alveolar proteinosis","termid":"MONDO:0012580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SFTPC- related interstitial lung disease","secondary_identifiers":["GARD:17744","Orphanet:440392"],"synonyms":[{"name":"SFTPC-related ILD","type":"exact"},{"name":"interstitial lung disease due to SP-C deficiency","type":"exact"},{"name":"interstitial lung disease due to surfactant protein C deficiency","type":"exact"}],"termid":"MONDO:0018603","xrefs":{"Monarch":{"xref_id":"0018603"}}}


id: GO:0102859
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a (9Z,12Z)-octadecadienoyl-containing glycerolipid + 2 Fe(II)-[cytochrome b5] + 2 H+ + O2 = (9Z,12Z,15Z)-octadecatrienoyl-containing glycerolipid + 2 Fe(III)-[cytochrome b5] + 2 H2O.","definition_xrefs":["RHEA:46404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water","termid":"GO:0016717"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"acyl-lipid omega-3 desaturase (cytochrome b5) activity","secondary_identifiers":["EC:1.14.19.25","MetaCyc:RXN-16046"],"synonyms":[{"name":"1-18:1-2-18:2-phosphatidylcholine desaturase activity (SN2-18:3 forming)","type":"exact"}],"termid":"GO:0102859"}


id: GO:0061731
data:
  {"annotated_genes":["SJAG_02948","SJAG_04665","SJAG_00885"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106732,91949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051063"},{"annotations":[71392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004748"}]},"cv_name":"molecular_function","definition":"Catalysis of the formation of 2'-deoxyribonucleoside diphosphate from ribonucleoside diphosphate, using either thioredoxin disulfide or glutaredoxin disulfide as an acceptor.","definition_xrefs":["PMID:16756507","GOC:dph","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH or CH2 groups, disulfide as acceptor","termid":"GO:0016728"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00885":null,"SJAG_02948":null,"SJAG_04665":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"ribonucleoside-diphosphate reductase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"RNR","type":"related"},{"name":"adenosylcobalamin-dependent ribonucleotide reductase activity","type":"related"},{"name":"aerobic non-heme iron-dependent ribonucleotide reductase activity","type":"related"},{"name":"anaerobic iron-sulfur-dependent ribonucleotide reductase activity","type":"related"},{"name":"class I ribonucleotide reductase activity","type":"related"},{"name":"class II ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"class II ribonucleotide reductase activity","type":"related"},{"name":"class III ribonucleotide reductase activity","type":"related"},{"name":"nucleoside diphosphate reductase activity","type":"related"},{"name":"purine/pyrimidine nucleoside diphosphate reduction","type":"related"},{"name":"ribonucleoside 5'-diphosphate reductase activity","type":"exact"},{"name":"ribonucleotide diphosphate reductase activity","type":"exact"},{"name":"ribonucleotide reductase activity","type":"broad"}],"termid":"GO:0061731","terms_by_termid":{"GO:0004748":null,"GO:0051063":null}}


id: PBO:0076384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transforming acidic coiled-coil containing protein 1 pseudogene 1","termid":"PBO:0076384"}


id: PBO:0017688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved protein Mug70","termid":"PBO:0017688"}


id: PBO:0063718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycolate phosphatase","termid":"PBO:0063718"}


id: GO:0055094
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 lipoprotein particle stimulus.","definition_xrefs":["GOC:rl","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to endogenous stimulus","termid":"GO:0009719"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to lipoprotein particle","synonyms":[{"name":"response to lipoprotein particle stimulus","type":"exact"}],"termid":"GO:0055094"}


id: GO:0106422
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: Zeaxanthin + O2 = (3R)-11-cis-3-hydroxyretinal + (3R)-all-trans-3-hydroxyretinal.","definition_xrefs":["RHEA:33931","PMID:19020100","PMID:19889630"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid dioxygenase activity","termid":"GO:0010436"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"carotenoid isomerooxygenase activity","secondary_identifiers":["EC:1.13.11.65"],"termid":"GO:0106422"}


id: PBO:0057064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 147a","termid":"PBO:0057064"}


id: FYPO:0002807
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 arsenate ions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal growth on arsenic","termid":"FYPO:0004368"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0002060","FYPO:0002057","FYPO:0000003","FYPO:0000257","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on arsenate","synonyms":[{"name":"normal cell population growth in presence of arsenate","type":"exact"},{"name":"normal cell population growth on arsenate","type":"exact"},{"name":"normal cell population growth on arsenate ion","type":"exact"},{"name":"normal cellular response to arsenate","type":"related"},{"name":"normal growth on arsenate ions","type":"exact"},{"name":"normal vegetative cell population growth on arsenate","type":"exact"}],"termid":"FYPO:0002807"}


id: PBO:0044540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DXZ4 associated non-coding transcript 1, proximal","termid":"PBO:0044540"}


id: MONDO:1012274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thrombopathia, non-human animal","termid":"MONDO:1011695"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombopathia, pig","secondary_identifiers":["OMIA:001003-9823"],"termid":"MONDO:1012274","xrefs":{"Monarch":{"xref_id":"1012274"}}}


id: MONDO:0003093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare carcinoma of the esophagus which contains squamous cells, mucus secreting cells, and cells of an intermediate type. (WHO)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucoepidermoid carcinoma","termid":"MONDO:0003036"},{"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":"mucoepidermoid esophageal carcinoma","secondary_identifiers":["DOID:4686","UMLS:C1333461","NCIT:C5343","MEDGEN:234232"],"synonyms":[{"name":"esophagus mucoepidermoid carcinoma","type":"exact"},{"name":"mucoepidermoid carcinoma of the esophagus","type":"exact"},{"name":"mucoepidermoid carcinoma of the oesophagus","type":"exact"},{"name":"oesophagus mucoepidermoid carcinoma","type":"exact"}],"termid":"MONDO:0003093","xrefs":{"Monarch":{"xref_id":"0003093"}}}


id: PBO:0029122
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-DNA_content_increased","termid":"PBO:0029122"}


id: MONDO:0007887
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked diffuse leiomyomatosis-Alport syndrome","termid":"MONDO:0010641"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"leiomyoma of vulva and esophagus","secondary_identifiers":["GARD:10097","MEDGEN:320616","UMLS:C1835488","MESH:C537006","OMIM:150700"],"synonyms":[{"name":"esophagogastric and vulvar leiomyomatosis","type":"related"},{"name":"leiomyoma of vulva and esophagus","type":"exact"},{"name":"leiomyomatosis, esophagogastric and vulvar","type":"related"}],"termid":"MONDO:0007887","xrefs":{"Monarch":{"xref_id":"0007887"}}}


id: GO:0021688
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the cerebellar molecular layer. This process pertains to the initial formation of a structure from unspecified parts. The molecular layer is the outermost layer of the cerebellar cortex. It contains the parallel fibers of the granule cells, interneurons such as stellate and basket cells, and the dendrites of the underlying Purkinje cells.","definition_xrefs":["GOC:dph","GO_REF:0000021","ISBN:0838580343","GOC:cls","GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"cerebellar molecular layer morphogenesis","termid":"GO:0021687"},{"relation_name":"part_of","term_name":"cerebellar cortex formation","termid":"GO:0021697"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebellar molecular layer formation","termid":"GO:0021688"}


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:0002039","MONDO:0000426","MONDO:0005559"],"is_obsolete":false,"name":"spinocerebellar ataxia type 35","secondary_identifiers":["UMLS:C3888031","icd11.foundation:1674449075","MEDGEN:854733","OMIM:613908","SCTID:719300001","DOID:0050982","GARD:12366"],"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: GO:0032207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a recombinational process involved in the maintenance of proper telomeric length.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic recombination","termid":"GO:0000019"},{"relation_name":"is_a","term_name":"regulation of telomere maintenance","termid":"GO:0032204"},{"relation_name":"is_a","term_name":"regulation of DNA recombination at telomere","termid":"GO:0072695"},{"relation_name":"regulates","term_name":"telomere maintenance via recombination","termid":"GO:0000722"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0032200"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006310","GO:0006259","GO:0008150","GO:0032200"],"is_obsolete":false,"name":"regulation of telomere maintenance via recombination","termid":"GO:0032207"}


id: PBO:0069334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 593, pseudogene","termid":"PBO:0069334"}


id: PBO:0000138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-fungal Zn(2)-Cys(6) binuclear cluster domain","termid":"PBO:0000138"}


id: PBO:0055087
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 2505","termid":"PBO:0055087"}


id: FYPO:0007874
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which exocytosis occurs to a lower extent than normal at the shmoo tip.","definition_xrefs":["PMID:34382996","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal exocytosis","termid":"FYPO:0007873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"decreased exocytosis at shmoo tip","synonyms":[{"name":"decreased exocytosis at mating projection tip","type":"exact"},{"name":"decreased exocytosis at shmoo projection","type":"exact"},{"name":"reduced exocytosis at shmoo tip","type":"exact"}],"termid":"FYPO:0007874"}


id: MONDO:0968979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"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 and seizures","secondary_identifiers":["OMIM:620790"],"termid":"MONDO:0968979","xrefs":{"Monarch":{"xref_id":"0968979"}}}


id: PBO:0074642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 35","termid":"PBO:0074642"}


id: PBO:0053710
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 919","termid":"PBO:0053710"}


id: MONDO:0004418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"infiltrating bladder urothelial carcinoma","termid":"MONDO:0003890"}],"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":"microcystic variant infiltrating bladder urothelial carcinoma","secondary_identifiers":["MEDGEN:268574","NCIT:C39820","UMLS:C1512740","DOID:7971"],"synonyms":[{"name":"infiltrating bladder urothelial carcinoma, microcystic variant","type":"exact"}],"termid":"MONDO:0004418","xrefs":{"Monarch":{"xref_id":"0004418"}}}


id: GO:0009969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of xyloglucan, the cross-linking glycan composed of (1->4)-beta-D glucan backbone substituted at regular intervals with beta-D-xylosyl-(1->6) residues, which is present in the primary cell wall of most higher plants.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucan biosynthetic process","termid":"GO:0009250"},{"relation_name":"is_a","term_name":"xyloglucan metabolic process","termid":"GO:0010411"},{"relation_name":"is_a","term_name":"cell wall polysaccharide biosynthetic process","termid":"GO:0070592"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0071554","GO:0008150"],"is_obsolete":false,"name":"xyloglucan biosynthetic process","synonyms":[{"name":"xyloglucan anabolism","type":"exact"},{"name":"xyloglucan biosynthesis","type":"exact"},{"name":"xyloglucan formation","type":"exact"},{"name":"xyloglucan synthesis","type":"exact"}],"termid":"GO:0009969"}


id: PBO:0082569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Checkpoint protein; involved in the activation of the DNA damage and meiotic pachytene checkpoints; subunit of a clamp loader that loads Rad17p-Mec3p-Ddc1p onto DNA; homolog of human and S. pombe Rad17 protein","termid":"PBO:0082569"}


id: GO:1900452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of long term synaptic depression.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synaptic plasticity","termid":"GO:0048167"},{"relation_name":"regulates","term_name":"long-term synaptic depression","termid":"GO:0060292"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of long-term synaptic depression","synonyms":[{"name":"regulation of LTD","type":"related"},{"name":"regulation of long term depression","type":"broad"},{"name":"regulation of long term synaptic depression","type":"exact"}],"termid":"GO:1900452"}


id: PBO:0057330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 520e","termid":"PBO:0057330"}


id: GO:0060200
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A clathrin-sculpted lipid bilayer membrane-enclosed vesicle after clathrin release and containing acetylcholine.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport vesicle","termid":"GO:0030133"},{"relation_name":"is_a","term_name":"clathrin-sculpted vesicle","termid":"GO:0060198"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0031410","GO:0005575"],"is_obsolete":false,"name":"clathrin-sculpted acetylcholine transport vesicle","synonyms":[{"name":"clathrin sculpted acetylcholine constitutive secretory pathway transport vesicle","type":"exact"},{"name":"clathrin sculpted acetylcholine transport vesicle","type":"exact"}],"termid":"GO:0060200"}


id: PR:Q10428
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- par1 gene.","definition_xrefs":["UniProtKB:Q10428","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":"serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta 1 isoform (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC188.02","synonyms":[{"name":"PP2A, B subunit, B' delta 1 isoform (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-par1","type":"exact"}],"termid":"PR:Q10428"}


id: MONDO:0015367
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Charlie M syndrome is a rare bone developmental disorder which belongs to a group of oromandibular limb hypogenesis syndromes that includes hypoglossia-hypodactyly and glossopalatine ankylosis. The major anomalies which occur commonly in this group are hypoplasia of the mandible, syndactyly and ectrodactyly, small mouth, cleft palate, hypodontia, and facial paralysis. Patients with Charlie M syndrome also present with hypertelorism, absent or conically crowned incisors, and variable degrees of hypodactyly of the hands and feet. There have been no further descriptions in the literature since 1976.","definition_xrefs":["Orphanet:1406"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"oromandibular-limb hypogenesis syndrome","termid":"MONDO:0017139"}],"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":"Charlie M syndrome","secondary_identifiers":["GARD:1261","MEDGEN:1379887","icd11.foundation:1284734481","UMLS:C4518555","SCTID:733034007"],"termid":"MONDO:0015367","xrefs":{"Monarch":{"xref_id":"0015367"}}}


id: GO:0140791
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H2AX serine phosphate (position 140) + H2O = histone H2AX serine (position 140) + phosphate.","definition_xrefs":["PMID:18614045"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone phosphatase activity","termid":"GO:0140789"}],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003674","GO:0016788","GO:0140096","GO:0016787","GO:0004721","GO:0003824"],"is_obsolete":false,"name":"histone H2AXS140 phosphatase activity","synonyms":[{"name":"histone H2-S140 serine phosphatase activity","type":"exact"},{"name":"histone H2S140 phosphatase activity","type":"related"},{"name":"histone serine phosphatase activity (H2-S140 specific)","type":"exact"}],"termid":"GO:0140791"}


id: GO:0045821
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of glycolysis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glycolytic process","termid":"GO:0006110"},{"relation_name":"is_a","term_name":"positive regulation of purine nucleotide catabolic process","termid":"GO:0033123"},{"relation_name":"is_a","term_name":"positive regulation of carbohydrate metabolic process","termid":"GO:0045913"},{"relation_name":"is_a","term_name":"positive regulation of ATP metabolic process","termid":"GO:1903580"},{"relation_name":"positively_regulates","term_name":"glycolytic process","termid":"GO:0006096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0005975"},{"rel_name":"positively_regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0005975","GO:0055086","GO:0008150","GO:0044281","GO:0006091"],"is_obsolete":false,"name":"positive regulation of glycolytic process","synonyms":[{"name":"activation of glycolysis","type":"narrow"},{"name":"stimulation of glycolysis","type":"narrow"},{"name":"up regulation of glycolysis","type":"exact"},{"name":"up-regulation of glycolysis","type":"exact"},{"name":"upregulation of glycolysis","type":"exact"}],"termid":"GO:0045821"}


id: PBO:0045669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein cytoplasmic 1 heavy chain 1","termid":"PBO:0045669"}


id: PBO:0051307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1/OR1-1 (pseudogene)","termid":"PBO:0051307"}


id: PBO:0085419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane transporter of the major facilitator superfamily; member of the 12-spanner drug:H(+) antiporter DHA1 family; exports copper; has broad substrate specificity and can transport many mono- and divalent cations; transports a variety of drugs and is required for resistance to quinidine, barban, cisplatin, and bleomycin; contributes to potassium homeostasis; expression is regulated by copper","termid":"PBO:0085419"}


id: FYPO:0003304
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A microtubule cytoskeleton organization phenotype observed in the vegetative growth phase of the life cycle in which formation of the mitotic spindle midzone, the area in the center of the mitotic spindle where the spindle microtubules from opposite poles overlap, is abnormal.","definition_xrefs":["GO:0051256","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic spindle elongation","termid":"FYPO:0000131"},{"relation_name":"is_a","term_name":"abnormal mitotic spindle assembly","termid":"FYPO:0000177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000337","FYPO:0001320","FYPO:0000631","FYPO:0000641","FYPO:0001985","FYPO:0000054"],"is_obsolete":false,"name":"abnormal mitotic spindle midzone assembly","synonyms":[{"name":"abnormal mitotic spindle midzone assembly during vegetative growth","type":"exact"},{"name":"abnormal spindle midzone assembly during mitotic cell cycle","type":"related"},{"name":"abnormal spindle midzone assembly involved in mitosis","type":"exact"}],"termid":"FYPO:0003304"}


id: PBO:0072556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RRAGAP1 antisense RNA 1","termid":"PBO:0072556"}


id: MONDO:0020068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"infectious encephalitis","termid":"MONDO:0020067"},{"relation_name":"is_a","term_name":"post-infectious disorder","termid":"MONDO:0021669"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postinfectious encephalitis","secondary_identifiers":["SCTID:192727001","UMLS:C0393459","DOID:10993","ICD9:323.6","MedDRA:10057235","MEDGEN:581376","Orphanet:98253"],"termid":"MONDO:0020068","xrefs":{"Monarch":{"xref_id":"0020068"}}}


id: PBO:0027312
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_5'_deoxyribonuclease_(pyrimidine_dimer)_activity","termid":"PBO:0027312"}


id: MONDO:0100374
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly t(16;16)(p13.1;q22). (A chromosomal translocation that involves chromosome 16. It is often associated with the development of acute myeloid leukemia CBFB-MYH11, acute myelomonocytic leukemia with abnormal eosinophils, and granulocytic sarcoma.)","definition_xrefs":["NCIT:C27759"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"acute myeloid leukemia, t(16;16)(p13.1;q22)","secondary_identifiers":["NCIT:C9019"],"synonyms":[{"name":"AML, t(16;16)(p13.1;q22)","type":"exact"},{"name":"AML, t(16;16)(p13.1;q22.1)","type":"exact"},{"name":"AML, t(16;16)(p13.1q22)","type":"exact"},{"name":"AML, t(16;16)(p13.1q22.1)","type":"exact"},{"name":"AML, t(16;16)(p13;q22)","type":"exact"},{"name":"AML, t(16;16)(p13q22)","type":"exact"}],"termid":"MONDO:0100374","xrefs":{"Monarch":{"xref_id":"0100374"}}}


id: PBO:0080792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XPC complex subunit, DNA damage recognition and repair factor","termid":"PBO:0080792"}


id: GO:0080031
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + methyl salicylate = H+ + methanol + salicylate.","definition_xrefs":["PMID:18467465","RHEA:33611","PMID:18643994"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"methyl salicylate esterase activity","secondary_identifiers":["MetaCyc:RXNQT-4366"],"synonyms":[{"name":"MESA esterase activity","type":"exact"},{"name":"methyl SA esterase activity","type":"exact"},{"name":"methylsalicylate esterase activity","type":"exact"},{"name":"salicylic acid methyl ester esterase activity","type":"exact"}],"termid":"GO:0080031"}


id: GO:0061507
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to 2',3' cyclic GMP-AMP (cGAMP) nucleotide, a cyclic purine dinucleotide that consists of AMP and GMP units cyclized via 2',5' and 3',5' linkages.","definition_xrefs":["GOC:dph","PMID:23258412","PMID:23910378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenyl ribonucleotide binding","termid":"GO:0032559"},{"relation_name":"is_a","term_name":"guanyl ribonucleotide binding","termid":"GO:0032561"},{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"cyclic GMP-AMP binding","termid":"GO:0140702"}],"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:0005488","GO:0003674"],"is_obsolete":false,"name":"2',3'-cyclic GMP-AMP binding","secondary_identifiers":["GO:0098546"],"synonyms":[{"name":"2',3' cGAMP binding","type":"exact"},{"name":"2',3' cyclic GAMP binding","type":"exact"},{"name":"2',3'-cGAMP binding","type":"exact"},{"name":"2',3'-cyclic GAMP binding","type":"exact"},{"name":"2',5-3',5'-cyclic GMP-AMP binding","type":"exact"},{"name":"c[G(2',5')pA(3',5')p] binding","type":"exact"},{"name":"cyclic-GMP-AMP binding","type":"broad"}],"termid":"GO:0061507"}


id: GO:0050748
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways involving lipoproteins, any conjugated, water-soluble protein in which the nonprotein group consists of a lipid or lipids.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lipoprotein metabolic process","termid":"GO:0050746"},{"relation_name":"is_a","term_name":"negative regulation of protein metabolic process","termid":"GO:0051248"},{"relation_name":"negatively_regulates","term_name":"lipoprotein metabolic process","termid":"GO:0042157"}],"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 lipoprotein metabolic process","synonyms":[{"name":"down regulation of lipoprotein metabolic process","type":"exact"},{"name":"down-regulation of lipoprotein metabolic process","type":"exact"},{"name":"downregulation of lipoprotein metabolic process","type":"exact"},{"name":"inhibition of lipoprotein metabolic process","type":"narrow"},{"name":"negative regulation of lipoprotein metabolism","type":"exact"}],"termid":"GO:0050748"}


id: MONDO:0005917
data:
  {"annotated_genes":["SJAG_01156"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032747"}]},"cv_name":"mondo","definition":"A disease involving the placenta.","direct_ancestors":[{"relation_name":"is_a","term_name":"uterine disorder","termid":"MONDO:0002654"},{"relation_name":"is_a","term_name":"pregnancy disorder","termid":"MONDO:0024575"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01156":null},"genotype_count":0,"is_obsolete":false,"name":"placenta disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:10781","UMLS:C0032045","MESH:D010922","NCIT:C26857","EFO:0007441","SCTID:125586008","ICD9:646.9","DOID:780","ICD9:656.70"],"synonyms":[{"name":"disease of placenta","type":"exact"},{"name":"disease or disorder of placenta","type":"exact"},{"name":"disease, placenta","type":"related"},{"name":"disease, placental","type":"related"},{"name":"diseases, placenta","type":"related"},{"name":"diseases, placental","type":"related"},{"name":"disorder of placenta","type":"exact"},{"name":"disorder, placenta","type":"related"},{"name":"disorders, placenta","type":"related"},{"name":"placenta disease","type":"exact"},{"name":"placenta disease or disorder","type":"exact"},{"name":"placenta diseases","type":"exact"},{"name":"placenta disorder","type":"exact"},{"name":"placenta disorders","type":"exact"},{"name":"placental disease","type":"related"},{"name":"placental diseases","type":"related"},{"name":"placental disorder","type":"exact"}],"termid":"MONDO:0005917","terms_by_termid":{"MONDO:0032747":null},"xrefs":{"Monarch":{"xref_id":"0005917"}}}


id: PBO:0027258
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_chromatin_at_tRNA_genes","termid":"PBO:0027258"}


id: GO:0022033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of microglial cells through the telencephalon.","definition_xrefs":["GO_REF:0000021","GOC:cls","GOC:jid","GOC:dph","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telencephalon glial cell migration","termid":"GO:0022030"}],"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":"telencephalon microglial cell migration","termid":"GO:0022033"}


id: SO:0001715
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An ISRE is a transcriptional cis regulatory region, containing the consensus region: YAGTTTC(A/T)YTTTYCC, responsible for increased transcription via interferon binding.","direct_ancestors":[{"relation_name":"is_a","term_name":"TF_binding_site","termid":"SO:0000235"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ISRE","synonyms":[{"name":"interferon stimulated response element","type":"exact"}],"termid":"SO:0001715"}


id: PR:Q10422
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC25G10.01 gene.","definition_xrefs":["UniProtKB:Q10422","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 RNA-binding protein C25G10.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25G10.01","synonyms":[{"name":"Spom972h-SPAC25G10.01","type":"exact"}],"termid":"PR:Q10422"}


id: PBO:0027017
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_telomeric_repeat_sequence","termid":"PBO:0027017"}


id: PBO:0085553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein constituent of 66S pre-ribosomal particles; contributes to processing of the 27S pre-rRNA; recruited by ribosomal proteins L17, L35, and L37 to assembling ribosomes after 27SB pre-rRNA is generated, immediately preceding removal of ITS2","termid":"PBO:0085553"}


id: PBO:0044914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DGAT2 divergent transcript","termid":"PBO:0044914"}


id: PBO:0112847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asynchronous replication autosomal RNA 8-1","termid":"PBO:0112847"}


id: FYPO:0004690
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 acetylation of lysine at position 9 of histone H3 at the silent mating-type cassettes occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 acetylation during vegetative growth","termid":"FYPO:0000892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0002274","FYPO:0000002"],"is_obsolete":false,"name":"increased histone H3-K9 acetylation at silent mating-type cassette during vegetative growth","synonyms":[{"name":"increased histone H3-K9 acetylation at mating-type region heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 acetylation at silent mating-type cassette during mitotic cell cycle","type":"related"},{"name":"increased histone H3K9 acetylation at silent mating-type cassette during vegetative growth","type":"exact"}],"termid":"FYPO:0004690"}


id: PBO:0076428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 11 like 4","termid":"PBO:0076428"}


id: GO:0004085
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: butanoyl-CoA + H+ + oxidized [electron-transfer flavoprotein] = (2E)-butenoyl-CoA + reduced [electron-transfer flavoprotein].","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete butyryl-CoA dehydrogenase activity (obsolete GO:0004085)","termid":"GO:0004085"}


id: GO:0071190
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the cell adhesion molecules protocadherin-alpha-v7 and protocadherin-gamma-b2, and is involved in the regulation of protein localization to the plasma membrane.","definition_xrefs":["PMID:15347688"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protocadherin-alpha-protocadherin-gamma complex","termid":"GO:0071183"}],"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:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"protocadherin-alpha-v7-protocadherin-gamma-b2 complex","synonyms":[{"name":"Pcdha7-Pcdhgb4 complex","type":"narrow"}],"termid":"GO:0071190"}


id: PBO:0039425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiopoietin like 5","termid":"PBO:0039425"}


id: PBO:0056303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule associated protein 2","termid":"PBO:0056303"}


id: PBO:0066860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 160","termid":"PBO:0066860"}


id: PBO:0005824
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5.1.1.1","termid":"PBO:0005824"}


id: PBO:0085219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Palmitoyltransferase that acts on transmembrane proteins; including the SNAREs Snc1p, Syn8p, Tlg1p and likely all SNAREs; contains an Asp-His-His-Cys-cysteine rich (DHHC-CRD) domain; may have a role in vacuole fusion","termid":"PBO:0085219"}


id: MONDO:0021132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An overproduction of parathyroid hormone that is autonomous and often associated with chronic secondary hyperparathyroidism.","definition_xrefs":["NCIT:C114821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperparathyroidism","termid":"MONDO:0001741"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tertiary hyperparathyroidism","secondary_identifiers":["ICD9:588.89","MEDGEN:488837","SCTID:78200003","icd11.foundation:10683191","UMLS:C0271858"],"synonyms":[{"name":"tertiary hyperparathyroidism","type":"exact"}],"termid":"MONDO:0021132","xrefs":{"Monarch":{"xref_id":"0021132"}}}


id: MONDO:0008115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies.","definition_xrefs":["Orphanet:391641"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Feingold syndrome","termid":"MONDO:0015267"}],"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":"Feingold syndrome type 1","secondary_identifiers":["ICD9:759.89","SCTID:702431004","UMLS:C4551774","OMIM:164280","MEDGEN:1637716","GARD:17624"],"synonyms":[{"name":"Brunner-Winter syndrome type 1","type":"exact"},{"name":"FGLDS1","type":"exact"},{"name":"FS1","type":"exact"},{"name":"Feingold syndrome","type":"related"},{"name":"Feingold syndrome 1","type":"related"},{"name":"Feingold syndrome caused by mutation in MYCN","type":"exact"},{"name":"Feingold syndrome type 1","type":"exact"},{"name":"MMT type 1","type":"exact"},{"name":"MODED syndrome type 1","type":"exact"},{"name":"MYCN Feingold syndrome","type":"exact"},{"name":"Mmt syndrome","type":"related"},{"name":"ODED syndrome type 1","type":"exact"},{"name":"Oded syndrome","type":"related"},{"name":"digital anomalies with short palpebral fissures and atresia of esophagus or duodenum","type":"related"},{"name":"digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1","type":"exact"},{"name":"digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum","type":"related"},{"name":"digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1","type":"exact"},{"name":"microcephaly and digital abnormalities with normal intelligence","type":"related"},{"name":"microcephaly, intellectual disability, and tracheoesophageal fistula syndrome","type":"related"},{"name":"microcephaly, mental retardation, and tracheoesophageal fistula syndrome","type":"related"},{"name":"microcephaly-digital anomalies-normal intelligence syndrome type 1","type":"exact"},{"name":"microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1","type":"exact"},{"name":"microcephaly-oculo-digito-esophageal-duodenal syndrome","type":"related"},{"name":"microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1","type":"exact"},{"name":"oculo-digito-esophageal-duodenal syndrome type 1","type":"exact"},{"name":"oculodigitoesophagoduodenal syndrome","type":"related"}],"termid":"MONDO:0008115","xrefs":{"Monarch":{"xref_id":"0008115"}}}


id: PATO:0001505
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's not being in contact with another entity, or of no longer being connected or joined with another entity.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"separated from","synonyms":[{"name":"discontiguous","type":"related"},{"name":"divided_from","type":"related"},{"name":"splitted from","type":"related"}],"termid":"PATO:0001505"}


id: MONDO:1040037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinopathy caused by autosomal recessive variants in the IMPG1 gene.","definition_xrefs":["PMID:23993198","PMID:28644393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0006025"],"is_obsolete":false,"name":"IMPG1-related recessive retinopathy","synonyms":[{"name":"IMPG1-related recessive retinopathy","type":"exact"}],"termid":"MONDO:1040037","xrefs":{"Monarch":{"xref_id":"1040037"}}}


id: PBO:0065461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PSMD6 antisense RNA 1","termid":"PBO:0065461"}


id: PBO:0040133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and SOCS box containing 17","termid":"PBO:0040133"}


id: MONDO:0018977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polyneuropathy associated with IgM monoclonal gammapathy (MG) with anti-MAG (myelin-associated-glycoprotein) activity is a demyelinating polyneuropathy characterized clinically by sensory ataxia, tremor, paresthesia, and impaired gait.","definition_xrefs":["Orphanet:639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired peripheral neuropathy","termid":"MONDO:0015923"}],"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":"polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG","secondary_identifiers":["MEDGEN:1434346","GARD:13173","UMLS:C1736154"],"synonyms":[{"name":"anti-MAG neuropathy","type":"exact"},{"name":"neuropathy associated with monoclonal IgM antibodies to myelin-associated glycoprotein","type":"exact"}],"termid":"MONDO:0018977","xrefs":{"Monarch":{"xref_id":"0018977"}}}


id: GO:0090229
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of the red or far-red signaling pathway, the series of molecular signals initiated upon sensing by photoreceptor molecules of red light or far red light.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of red or far-red light signaling pathway","termid":"GO:0090227"},{"relation_name":"negatively_regulates","term_name":"red or far-red light signaling pathway","termid":"GO:0010017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of red or far-red light signaling pathway","synonyms":[{"name":"negative regulation of phytochrome signaling pathway","type":"exact"},{"name":"negative regulation of red or far-red light signalling pathway","type":"exact"}],"termid":"GO:0090229"}


id: GO:0001666
data:
  {"annotated_genes":["SJAG_01150","SJAG_01585","SJAG_00221","SJAG_03345","SJAG_00642","SJAG_04018"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109310,116428,100711,111162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[88775,115838],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1900039"}]},"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 stimulus indicating lowered oxygen tension. Hypoxia, defined as a decline in O2 levels below normoxic levels of 20.8 - 20.95%, results in metabolic adaptation at both the cellular and organismal level.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"response to decreased oxygen levels","termid":"GO:0036293"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00221":null,"SJAG_00642":null,"SJAG_01150":null,"SJAG_01585":null,"SJAG_03345":null,"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to hypoxia","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"response to hypoxic stress","type":"exact"},{"name":"response to intermittent hypoxia","type":"narrow"},{"name":"response to lowered oxygen tension","type":"exact"},{"name":"response to sustained hypoxia","type":"narrow"}],"termid":"GO:0001666","terms_by_termid":{"GO:0071456":null,"GO:1900039":null}}


id: GO:0090674
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The binding of an endothelial cell to the extracellular matrix via fibronectin.","definition_xrefs":["PMID:19460962","GOC:BHF","GOC:bc","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell-matrix adhesion","termid":"GO:0090673"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"endothelial cell-matrix adhesion via fibronectin","termid":"GO:0090674"}


id: PBO:0053664
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 841","termid":"PBO:0053664"}


id: PBO:0077104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIMM9 pseudogene 2","termid":"PBO:0077104"}


id: MONDO:0003273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the sternum","direct_ancestors":[{"relation_name":"is_a","term_name":"bone cancer","termid":"MONDO:0002129"},{"relation_name":"is_a","term_name":"thoracic cancer","termid":"MONDO:0003274"},{"relation_name":"is_a","term_name":"sternal neoplasm","termid":"MONDO:0021578"}],"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":"sternum cancer","secondary_identifiers":["NCIT:C8408","DOID:5090","MEDGEN:277996","UMLS:C1382025"],"synonyms":[{"name":"cancer of sternum","type":"exact"},{"name":"malignant neoplasm of sternum","type":"exact"},{"name":"malignant neoplasm of the sternum","type":"exact"},{"name":"malignant sternal neoplasm","type":"exact"},{"name":"malignant sternal tumor","type":"exact"},{"name":"malignant sternal tumour","type":"exact"},{"name":"malignant sternum neoplasm","type":"exact"},{"name":"malignant tumor of sternum","type":"exact"},{"name":"malignant tumor of the sternum","type":"exact"},{"name":"malignant tumour of sternum","type":"exact"},{"name":"malignant tumour of the sternum","type":"exact"},{"name":"neoplasm of sternum","type":"broad"},{"name":"sternal tumour","type":"broad"},{"name":"sternum cancer","type":"exact"}],"termid":"MONDO:0003273","xrefs":{"Monarch":{"xref_id":"0003273"}}}


id: GO:1904099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein O-linked glycosylation.","definition_xrefs":["GO_REF:0000058","PMID:24509081","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein glycosylation","termid":"GO:0060051"},{"relation_name":"is_a","term_name":"regulation of protein O-linked glycosylation","termid":"GO:1904098"},{"relation_name":"negatively_regulates","term_name":"protein O-linked glycosylation","termid":"GO:0006493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006486"},{"rel_name":"negatively_regulates","termid":"GO:0006486"}],"interesting_parent_ids":["GO:0008150","GO:0006486"],"is_obsolete":false,"name":"negative regulation of protein O-linked glycosylation","synonyms":[{"name":"down regulation of protein O-linked glycosylation","type":"exact"},{"name":"down regulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"down-regulation of protein O-linked glycosylation","type":"exact"},{"name":"down-regulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"downregulation of protein O-linked glycosylation","type":"exact"},{"name":"downregulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"inhibition of protein O-linked glycosylation","type":"narrow"},{"name":"inhibition of protein amino acid O-linked glycosylation","type":"narrow"},{"name":"negative regulation of protein amino acid O-linked glycosylation","type":"exact"}],"termid":"GO:1904099"}


id: GO:1901380
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of potassium ion transmembrane transport.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of potassium ion transport","termid":"GO:0043267"},{"relation_name":"is_a","term_name":"regulation of potassium ion transmembrane transport","termid":"GO:1901379"},{"relation_name":"is_a","term_name":"negative regulation of cation transmembrane transport","termid":"GO:1904063"},{"relation_name":"negatively_regulates","term_name":"potassium ion transmembrane transport","termid":"GO:0071805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of potassium ion transmembrane transport","synonyms":[{"name":"down regulation of potassium ion transmembrane transport","type":"exact"},{"name":"down-regulation of potassium ion transmembrane transport","type":"exact"},{"name":"downregulation of potassium ion transmembrane transport","type":"exact"},{"name":"inhibition of potassium ion transmembrane transport","type":"narrow"},{"name":"negative regulation of potassium ion membrane transport","type":"exact"}],"termid":"GO:1901380"}


id: PBO:0001177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate-tRNA ligase (predicted)","termid":"PBO:0001177"}


id: MONDO:0013235
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial pancreatic carcinoma in which the cause of the disease is a mutation in the BRCA2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"familial pancreatic carcinoma","termid":"MONDO:0015278"},{"relation_name":"is_a","term_name":"BRCA2-related cancer predisposition","termid":"MONDO:0700269"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pancreatic cancer, susceptibility to, 2","secondary_identifiers":["MEDGEN:461896","OMIM:613347","UMLS:C3150546"],"synonyms":[{"name":"BRCA2 familial pancreatic carcinoma","type":"exact"},{"name":"Pnca2","type":"related"},{"name":"familial pancreatic carcinoma caused by mutation in BRCA2","type":"exact"},{"name":"pancreatic cancer 2","type":"exact"},{"name":"pancreatic cancer, susceptibility to, 2","type":"exact"},{"name":"pancreatic cancer, susceptibility to, type 2","type":"exact"},{"name":"susceptibility to pancreatic cancer 2","type":"related"}],"termid":"MONDO:0013235","xrefs":{"Monarch":{"xref_id":"0013235"}}}


id: GO:0050931
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a pigmented cell, such as a melanocyte.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"developmental pigmentation","termid":"GO:0048066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"pigment cell differentiation","secondary_identifiers":["GO:0043357","GO:0043358"],"synonyms":[{"name":"chromatophore differentiation","type":"exact"},{"name":"pigmented cell differentiation","type":"exact"}],"termid":"GO:0050931"}


id: GO:2000408
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of T cell extravasation.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular extravasation","termid":"GO:0002692"},{"relation_name":"is_a","term_name":"negative regulation of T cell migration","termid":"GO:2000405"},{"relation_name":"is_a","term_name":"regulation of T cell extravasation","termid":"GO:2000407"},{"relation_name":"negatively_regulates","term_name":"T cell extravasation","termid":"GO:0072683"}],"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 T cell extravasation","synonyms":[{"name":"negative regulation of T lymphocyte extravasation","type":"exact"},{"name":"negative regulation of T-cell extravasation","type":"exact"},{"name":"negative regulation of T-lymphocyte extravasation","type":"exact"}],"termid":"GO:2000408"}


id: FYPO:0005803
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 movement of one or more proteins within the plasma membrane of the lateral part of the cell occurs more slowly than normal.","definition_xrefs":["PomBase:mah","PMID:25837586"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein movement within plasma membrane during vegetative growth","termid":"FYPO:0005800"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased rate of protein movement within plasma membrane at cell side","synonyms":[{"name":"decreased rate of protein movement within plasma membrane at cell side during mitotic cell cycle","type":"related"},{"name":"decreased rate of protein movement within plasma membrane at cell side during vegetative growth","type":"exact"},{"name":"decreased rate of protein movement within plasma membrane at lateral part of cell","type":"exact"},{"name":"reduced rate of protein movement within plasma membrane at cell side","type":"exact"},{"name":"slow protein movement within plasma membrane at cell side","type":"exact"}],"termid":"FYPO:0005803"}


id: PBO:0063930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paired immunoglobin like type 2 receptor alpha","termid":"PBO:0063930"}


id: GO:0005185
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action characteristic of a neurohypophyseal hormone, any of a family of structurally and functionally related nonapeptides that are synthesized as part of a larger precursor molecule comprising a signal peptide, the nonapeptide hormone, and a neurophysin.","definition_xrefs":["PMID:19243634","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide hormone activity","termid":"GO:0005184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0140677"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0098772","GO:0005488","GO:0140677"],"is_obsolete":false,"name":"neurohypophyseal hormone activity","synonyms":[{"name":"neurohypophysial hormone activity","type":"exact"}],"termid":"GO:0005185"}


id: PBO:0110973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF4504 family protein, human C1orf74 ortholog, implicated in transcription or signalling, possibly phosphate starvation response","termid":"PBO:0110973"}


id: PATO:0002128
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering a bearer by virtue of the bearer's containing or resembling serum.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"composition","termid":"PATO:0000025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serous","termid":"PATO:0002128"}


id: MONDO:0023039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"eccrine carcinoma","termid":"MONDO:0024240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"eccrine mucinous carcinoma","secondary_identifiers":["UMLS:C0346020","MEDGEN:577240"],"termid":"MONDO:0023039","xrefs":{"Monarch":{"xref_id":"0023039"}}}


id: GO:0047981
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-histidine + acetyl-CoA = N(alpha)-acetyl-L-histidine + CoA + H+.","definition_xrefs":["RHEA:24596","EC:2.3.1.33"],"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: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:0016746","GO:0003824"],"is_obsolete":false,"name":"histidine N-acetyltransferase activity","secondary_identifiers":["MetaCyc:HISTIDINE-N-ACETYLTRANSFERASE-RXN","KEGG_REACTION:R01160"],"synonyms":[{"name":"acetyl-CoA:L-histidine N-acetyltransferase activity","type":"related"},{"name":"acetylhistidine synthetase activity","type":"related"},{"name":"histidine acetyltransferase activity","type":"related"}],"termid":"GO:0047981"}


id: PBO:0005308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin Snx12 (predicted)","termid":"PBO:0005308"}


id: PBO:0060349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYO16 antisense RNA 1","termid":"PBO:0060349"}


id: PBO:0040493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxin 10","termid":"PBO:0040493"}


id: GO:0080148
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a response to water deprivation. Response to water deprivation is 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 water deprivation stimulus, prolonged deprivation of water.","definition_xrefs":["PMID:18835996"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of response to water deprivation","termid":"GO:2000070"},{"relation_name":"negatively_regulates","term_name":"response to water deprivation","termid":"GO:0009414"}],"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 response to water deprivation","termid":"GO:0080148"}


id: PBO:0113050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Co-chaperone that binds Hsp82p and activates its ATPase activity; plays a role in determining prion variants; similar to Hch1p; involved in the nuclear import of Hsp82p after DNA damage; expression is regulated by stresses such as heat shock; protein abundance increases in response to DNA replication stress","termid":"PBO:0113050"}


id: GO:0034591
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the rhoptry membrane.","definition_xrefs":["GOC:rph","PMID:17997128"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle lumen","termid":"GO:0043233"},{"relation_name":"part_of","term_name":"rhoptry","termid":"GO:0020008"}],"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":"rhoptry lumen","termid":"GO:0034591"}


id: PBO:0090827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex platform subcomplex scaffold TPR subunit Apc5","termid":"PBO:0090827"}


id: PBO:0003346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TENA/THI family protein","termid":"PBO:0003346"}


id: PBO:0048876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A6 family member B","termid":"PBO:0048876"}


id: PBO:0004240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human C17orf28 ortholog 2","termid":"PBO:0004240"}


id: GO:0031699
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a beta-3 adrenergic receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adrenergic receptor binding","termid":"GO:0031690"}],"gene_count":0,"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:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"beta-3 adrenergic receptor binding","synonyms":[{"name":"beta-3 adrenergic receptor ligand","type":"narrow"}],"termid":"GO:0031699"}


id: PBO:0111309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase chadoprop types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UniProt-GOA_version","termid":"PBO:0111309"}


id: GO:0072040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces the occurrence or rate of mesenchymal stem cell death by apoptotic process that contributes to the shaping of the nephron.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal cell apoptotic process involved in nephron morphogenesis","termid":"GO:0072039"},{"relation_name":"is_a","term_name":"negative regulation of apoptotic process involved in morphogenesis","termid":"GO:1902338"},{"relation_name":"is_a","term_name":"negative regulation of somatic stem cell population maintenance","termid":"GO:1904673"},{"relation_name":"is_a","term_name":"negative regulation of mesenchymal cell apoptotic process","termid":"GO:2001054"},{"relation_name":"negatively_regulates","term_name":"mesenchymal stem cell maintenance involved in nephron morphogenesis","termid":"GO:0072038"},{"relation_name":"negatively_regulates","term_name":"mesenchymal cell apoptotic process involved in nephron morphogenesis","termid":"GO:1901145"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of mesenchymal cell apoptotic process involved in nephron morphogenesis","synonyms":[{"name":"negative regulation of mesenchymal stem cell apoptosis involved in nephron morphogenesis","type":"narrow"},{"name":"negative regulation of mesenchymal stem cell apoptotic process involved in nephron morphogenesis","type":"exact"}],"termid":"GO:0072040"}


id: PBO:0061607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear casein kinase and cyclin dependent kinase substrate 1","termid":"PBO:0061607"}


id: GO:1902240
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator.","definition_xrefs":["GOC:krc","GOC:TermGenie","PMID:16571598","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of intrinsic apoptotic signaling pathway in response to osmotic stress","termid":"GO:1902220"},{"relation_name":"is_a","term_name":"regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator","termid":"GO:1902238"},{"relation_name":"is_a","term_name":"positive regulation of intrinsic apoptotic signaling pathway by p53 class mediator","termid":"GO:1902255"},{"relation_name":"positively_regulates","term_name":"intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator","termid":"GO:1990127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator","synonyms":[{"name":"activation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator","type":"narrow"},{"name":"up regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator","type":"exact"},{"name":"up-regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator","type":"exact"},{"name":"upregulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator","type":"exact"}],"termid":"GO:1902240"}


id: MONDO:0013739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any chilblain lupus in which the cause of the disease is a mutation in the SAMHD1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial chilblain lupus","termid":"MONDO:0018827"},{"relation_name":"is_a","term_name":"SAMHD1-related type 1 interferonopathy","termid":"MONDO:0700260"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"chilblain lupus 2","secondary_identifiers":["GARD:18494","OMIM:614415","UMLS:C3280721","MEDGEN:482351"],"synonyms":[{"name":"CHBL2","type":"related"},{"name":"Chilblain lupus type 2","type":"exact"},{"name":"SAMHD1 chilblain lupus","type":"exact"},{"name":"chilblain lupus 2","type":"exact"},{"name":"chilblain lupus caused by mutation in SAMHD1","type":"exact"}],"termid":"MONDO:0013739","xrefs":{"Monarch":{"xref_id":"0013739"}}}


id: PBO:0076863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 13A","termid":"PBO:0076863"}


id: PR:Q9Y7J6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppk21 gene.","definition_xrefs":["UniProtKB:Q9Y7J6","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":"serine/threonine-protein kinase ppk21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1778.10c","synonyms":[{"name":"Spom972h-ppk21","type":"exact"}],"termid":"PR:Q9Y7J6"}


id: PBO:0003773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin C-terminal hydrolase Ubp4","termid":"PBO:0003773"}


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


id: GO:0090540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cellulose, a linear beta1-4 glucan of molecular mass 50-400 kDa with the pyranose units in the -4C1 conformation, as it occurs in certain types of bacteria, mainly Acetobacter, Sarcina ventriculi and Agrobacteria.","definition_xrefs":["GOC:yaf","PMID:24097954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellulose biosynthetic process","termid":"GO:0030244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"bacterial cellulose biosynthetic process","synonyms":[{"name":"bacterial cellulose biosynthesis","type":"exact"}],"termid":"GO:0090540"}


id: MONDO:0014366
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any azoospermia in which the cause of the disease is a mutation in the ZMYND15 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 14","secondary_identifiers":["GARD:16020","MEDGEN:862891","OMIM:615842","UMLS:C4014454","DOID:0070179"],"synonyms":[{"name":"SPGF14","type":"related"},{"name":"ZMYND15 azoospermia","type":"exact"},{"name":"azoospermia caused by mutation in ZMYND15","type":"exact"},{"name":"spermatogenic failure 14","type":"exact"},{"name":"spermatogenic failure type 14","type":"exact"}],"termid":"MONDO:0014366","xrefs":{"Monarch":{"xref_id":"0014366"}}}


id: MONDO:0017101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated focal cortical dysplasia type II","termid":"MONDO:0011818"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"isolated focal cortical dysplasia type IIa","secondary_identifiers":["Orphanet:269001","UMLS:C1846386","NANDO:1200568","GARD:17270","MEDGEN:375876"],"synonyms":[{"name":"FCD type IIa","type":"exact"}],"termid":"MONDO:0017101","xrefs":{"Monarch":{"xref_id":"0017101"}}}


id: MONDO:0859183
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":"Parkinson disease 24, autosomal dominant, susceptibility to","secondary_identifiers":["UMLS:C5561969","MEDGEN:1794179","OMIM:619491"],"termid":"MONDO:0859183","xrefs":{"Monarch":{"xref_id":"0859183"}}}


id: MONDO:0015485
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary hereditary glaucoma (obsolete MONDO:0015485)","secondary_identifiers":["Orphanet:156005"],"synonyms":[{"name":"primary glaucoma","type":"related"}],"termid":"MONDO:0015485","xrefs":{"Monarch":{"xref_id":"0015485"}}}


id: PBO:0068438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 8, pseudogene","termid":"PBO:0068438"}


id: PBO:0088265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminotransferase, class I/classII","termid":"PBO:0088265"}


id: GO:0045631
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mechanoreceptor differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neuron differentiation","termid":"GO:0045664"},{"relation_name":"regulates","term_name":"mechanoreceptor differentiation","termid":"GO:0042490"}],"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 mechanoreceptor differentiation","termid":"GO:0045631"}


id: GO:2000853
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of corticosterone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glucocorticoid secretion","termid":"GO:2000850"},{"relation_name":"is_a","term_name":"regulation of corticosterone secretion","termid":"GO:2000852"},{"relation_name":"negatively_regulates","term_name":"corticosterone secretion","termid":"GO:0035934"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"negative regulation of corticosterone secretion","termid":"GO:2000853"}


id: PBO:0072633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arginine and serine rich protein 1","termid":"PBO:0072633"}


id: GO:0021853
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of GABAergic interneuron precursors from the subpallium to the cerebral cortex.","definition_xrefs":["GOC:jid","PMID:12626695","GO_REF:0000021","GOC:dgh","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interneuron migration from the subpallium to the cortex","termid":"GO:0021830"},{"relation_name":"is_a","term_name":"interneuron migration","termid":"GO:1904936"},{"relation_name":"part_of","term_name":"cerebral cortex GABAergic interneuron development","termid":"GO:0021894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebral cortex GABAergic interneuron migration","termid":"GO:0021853"}


id: MONDO:0012089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ichthyosis prematurity syndrome is a rare, syndromic congenital ichthyosis characterized by premature birth (at gestational weeks 30-32, in general) in addition to thick, caseous and desquamating epidermis, neonatal respiratory asphyxia, and persistent eosinophilia. After the perinatal period, a spontaneous improvement in the health of affected patients is observed and skin features (vernix caseosa-like scale) evolve into a mild presentation of flat follicular hyperkeratosis with atopy.","definition_xrefs":["Orphanet:88621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"pneumonitis","termid":"MONDO:0043905"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ichthyosis prematurity syndrome","secondary_identifiers":["OMIM:608649","SCTID:12381000132107","UMLS:C1837610","MESH:C536271","GARD:9886","MEDGEN:324839","NCIT:C62590"],"synonyms":[{"name":"IPS","type":"exact"},{"name":"congenital ichthyosis type 4","type":"exact"},{"name":"ichthyosis congenita 4","type":"related"},{"name":"ichthyosis congenita IV","type":"related"},{"name":"ichthyosis prematurity syndrome","type":"exact"},{"name":"ichthyosis-prematurity syndrome","type":"related"},{"name":"idiopathic pneumonia syndrome","type":"exact"}],"termid":"MONDO:0012089","xrefs":{"Monarch":{"xref_id":"0012089"}}}


id: FYECO:0000165
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which sodium sulfide (Na2S) was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ Na2S","synonyms":[{"name":"sodium sulfide added","type":"exact"}],"termid":"FYECO:0000165"}


id: SO:1000030
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An interchromosomal mutation where a region of the chromosome is inverted with respect to wild type.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inversion","termid":"SO:1000036"},{"relation_name":"is_a","term_name":"intrachromosomal_mutation","termid":"SO:1000028"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosomal_inversion","secondary_identifiers":["http://en.wikipedia.org/wiki/Chromosomal_inversion"],"synonyms":[{"name":"(Drosophila)In","type":"related"},{"name":"(bacteria)IN","type":"related"},{"name":"(fungi)In","type":"related"},{"name":"chromosomal inversion","type":"exact"}],"termid":"SO:1000030"}


id: GO:0002564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The generation of alternate transcripts of immunoglobulin genes through alternate splicing of exons.","definition_xrefs":["PMID:9185563","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of immune receptors via alternate splicing","termid":"GO:0002563"},{"relation_name":"is_a","term_name":"somatic diversification of immunoglobulins","termid":"GO:0016445"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"alternate splicing of immunoglobulin genes","synonyms":[{"name":"alternate splicing of antibody genes","type":"exact"}],"termid":"GO:0002564"}


id: GO:0062206
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 8-hydroxycopalyl diphosphate = (13R)-manoyl oxide + diphosphate.","definition_xrefs":["PMID:24990389","RHEA:54516"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"manoyl oxide synthase activity","secondary_identifiers":["EC:4.2.3.190"],"termid":"GO:0062206"}


id: PBO:0057494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 612","termid":"PBO:0057494"}


id: MONDO:0002160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cerebral palsy (obsolete MONDO:0002160)","termid":"MONDO:0002160","xrefs":{"Monarch":{"xref_id":"0002160"}}}


id: PBO:0003750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L17","termid":"PBO:0003750"}


id: PBO:0090185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-O","termid":"PBO:0090185"}


id: MONDO:0018115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by lesions occurring on the face, scalp, or neck which consist of congenital hypoplastic malformations of cutaneous structures and which over time undergo verrucous hyperplasia. Additionally it is associated with neurological symptoms and skeletal, ophthalmological, urogenital, and cardiovascular abnormalities.","definition_xrefs":["MESH:D054000"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"melanocytic nevus","termid":"MONDO:0005073"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidermal nevus syndrome","secondary_identifiers":["Orphanet:35125","MedDRA:10014985","MEDGEN:1847175","GARD:18813","SCTID:239112008","UMLS:C5848385"],"synonyms":[{"name":"Epidermal hamartoma syndrome","type":"exact"}],"termid":"MONDO:0018115","xrefs":{"Monarch":{"xref_id":"0018115"}}}


id: PBO:0029056
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-large_vacuoles_present_in_decreased_numbers_during_vegetative_growth","termid":"PBO:0029056"}


id: GO:1902832
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cell proliferation in dorsal spinal cord.","definition_xrefs":["GOC:TermGenie","PMID:21730158","GO_REF:0000058","GOC:mr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell proliferation in dorsal spinal cord","termid":"GO:0021921"},{"relation_name":"is_a","term_name":"negative regulation of neural precursor cell proliferation","termid":"GO:2000178"},{"relation_name":"negatively_regulates","term_name":"cell proliferation in dorsal spinal cord","termid":"GO:0010456"}],"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 cell proliferation in dorsal spinal cord","synonyms":[{"name":"down regulation of cell proliferation in dorsal spinal cord","type":"exact"},{"name":"down-regulation of cell proliferation in dorsal spinal cord","type":"exact"},{"name":"downregulation of cell proliferation in dorsal spinal cord","type":"exact"},{"name":"inhibition of cell proliferation in dorsal spinal cord","type":"narrow"}],"termid":"GO:1902832"}


id: FYECO:0000176
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which ethylenediaminetetraacetic acid (EDTA) was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ EDTA","synonyms":[{"name":"EDTA added","type":"exact"},{"name":"ethylenediaminetetraacetic acid added","type":"exact"}],"termid":"FYECO:0000176"}


id: PBO:0028475
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_NADH_dehydrogenase_(ubiquinone)_activity","termid":"PBO:0028475"}


id: PBO:0039130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminoacyl tRNA synthetase complex interacting multifunctional protein 1","termid":"PBO:0039130"}


id: PBO:0085529
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 S28, no bacterial homolog; has an extraribosomal function in autoregulation, in which Rps28Bp binds to a decapping complex via Edc3p, which then binds to RPS28B mRNA leading to its decapping and degradation; RPS28B has a paralog, RPS28A, that arose from the whole genome duplication","termid":"PBO:0085529"}


id: PBO:0068552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 3, pseudogene","termid":"PBO:0068552"}


id: PBO:0078537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 29","termid":"PBO:0078537"}


id: PBO:0073773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 4 member 7","termid":"PBO:0073773"}


id: PBO:0113030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic subunit of the DNA polymerase I alpha-primase complex; required for the initiation of DNA replication during mitotic DNA synthesis and premeiotic DNA synthesis; H3-H4 histone chaperone, downstream of Pol32p, involved in the transfer of parental histones to the lagging strand during DNA replication","termid":"PBO:0113030"}


id: SO:0002333
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A stop codon with the DNA sequence TAG.","direct_ancestors":[{"relation_name":"is_a","term_name":"stop_codon","termid":"SO:0000319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amber_stop_codon","synonyms":[{"name":"Amber stop codon","type":"exact"}],"termid":"SO:0002333"}


id: PBO:0047606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FHL1 pseudogene 1","termid":"PBO:0047606"}


id: MONDO:0002227
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma that affects the ovary. Lymphomatous involvement of the ovary is rare and in approximately half of the cases both ovaries are affected.","definition_xrefs":["NCIT:C40021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma","termid":"MONDO:0005062"},{"relation_name":"is_a","term_name":"ovarian cancer","termid":"MONDO:0008170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"ovarian lymphoma","secondary_identifiers":["DOID:2150","MEDGEN:276669","UMLS:C1518720"],"synonyms":[{"name":"lymphoma of ovary","type":"exact"},{"name":"ovarian lymphoma","type":"exact"},{"name":"ovary lymphoma","type":"exact"},{"name":"primary ovarian lymphoma","type":"exact"}],"termid":"MONDO:0002227","xrefs":{"Monarch":{"xref_id":"0002227"}}}


id: GO:0071918
data:
  {"annotated_genes":["SJAG_02125"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106548],"is_not":false,"summary":null,"term":"GO:0071918"}]},"cv_name":"biological_process","definition":"The process in which urea, the water-soluble compound H2N-CO-NH2, is transported from one side of a membrane to the other by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urea transport","termid":"GO:0015840"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02125":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"urea transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"urea membrane transport","type":"exact"}],"termid":"GO:0071918","terms_by_termid":{"GO:0071918":null}}


id: PBO:0039451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and MYND domain containing 2","termid":"PBO:0039451"}


id: PBO:0070221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 154 pseudogene","termid":"PBO:0070221"}


id: PBO:0090993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HbrB family protein involved in TOR signaling Bit2","termid":"PBO:0090993"}


id: PBO:0041525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 16 open reading frame 86","termid":"PBO:0041525"}


id: MONDO:0044622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"EMILIN-1-related connective tissue disease","secondary_identifiers":["UMLS:C5681244","GARD:21994","Orphanet:485418","MEDGEN:1814474"],"termid":"MONDO:0044622","xrefs":{"Monarch":{"xref_id":"0044622"}}}


id: GO:0019290
data:
  {"annotated_genes":["SJAG_00792","SJAG_04031","SJAG_00469","SJAG_04032"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104865],"is_not":false,"summary":null,"term":"GO:0019290"},{"annotations":[93618,93610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031169"},{"annotations":[93564],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905569"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of siderophores, low molecular weight Fe(III)-chelating substances made by aerobic or facultatively anaerobic bacteria, especially when growing under iron deficient conditions. The complexes of Fe(3+)-siderophores have very high stability constants and are taken up by specific transport systems by microorganisms; the subsequent release of iron requires enzymatic action.","definition_xrefs":["PMID:20376388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore metabolic process","termid":"GO:0009237"},{"relation_name":"is_a","term_name":"nonribosomal peptide biosynthetic process","termid":"GO:0019184"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00469":null,"SJAG_00792":null,"SJAG_04031":null,"SJAG_04032":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"siderophore biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0031178","GO:0031180"],"synonyms":[{"name":"siderochrome biosynthesis","type":"narrow"},{"name":"siderochrome biosynthetic process","type":"narrow"},{"name":"siderophore anabolism","type":"exact"},{"name":"siderophore biosynthesis","type":"exact"},{"name":"siderophore biosynthetic process, peptide formation","type":"narrow"},{"name":"siderophore biosynthetic process, peptide modification","type":"narrow"},{"name":"siderophore formation","type":"exact"},{"name":"siderophore synthesis","type":"exact"}],"termid":"GO:0019290","terms_by_termid":{"GO:0019290":null,"GO:0031169":null,"GO:1905569":null}}


id: GO:0071540
data:
  {"annotated_genes":["SJAG_02164","SJAG_02995","SJAG_03472","SJAG_03147","SJAG_04981","SJAG_04744","SJAG_02376","SJAG_02628"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[94291,97228,97287,98429,104788,105074,110147,110789],"is_not":false,"summary":null,"term":"GO:0071540"}]},"cv_name":"cellular_component","definition":"An eukaryotic translation initiation factor 3 complex that contains the PCI-domain protein eIF3e.","definition_xrefs":["PMID:15904532","PMID:19061185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eukaryotic translation initiation factor 3 complex","termid":"GO:0005852"}],"gene_count":8,"genes_by_uniquename":{"SJAG_02164":null,"SJAG_02376":null,"SJAG_02628":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03472":null,"SJAG_04744":null,"SJAG_04981":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 complex, eIF3e","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"eIF3e-containing eukaryotic translation initiation factor 3 complex","type":"exact"}],"termid":"GO:0071540","terms_by_termid":{"GO:0071540":null}}


id: PBO:0061011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicolin 1, tubulin polyglutamylase complex subunit","termid":"PBO:0061011"}


id: PBO:0046486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERCC8 antisense RNA 1","termid":"PBO:0046486"}


id: PBO:0088875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidinol dehydrogenase His2","termid":"PBO:0088875"}


id: MONDO:0800419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast cancer, familial, susceptibility to, 2","termid":"MONDO:0800419","xrefs":{"Monarch":{"xref_id":"0800419"}}}


id: PBO:0069975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1270, pseudogene","termid":"PBO:0069975"}


id: SO:0000050
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A part of a gene, that has no other route in the ontology back to region. This concept is necessary for logical inference as these parts must have the properties of region. It also allows us to associate all the parts of genes with a gene.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000050 gene_part (obsolete SO:0000050)","termid":"SO:0000050"}


id: GO:0007170
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete transmembrane receptor protein tyrosine kinase ligand binding (obsolete GO:0007170)","synonyms":[{"name":"transmembrane receptor protein tyrosine kinase ligand binding","type":"exact"}],"termid":"GO:0007170"}


id: PBO:0064356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phorbol-12-myristate-13-acetate-induced protein 1","termid":"PBO:0064356"}


id: GO:0018495
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-hydroxycyclohexane-1-carboxyl-CoA = 2 H+ + 2 e- + 2-ketocyclohexane-1-carboxyl-CoA.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-hydroxycyclohexane-1-carboxyl-CoA dehydrogenase activity (obsolete GO:0018495)","termid":"GO:0018495"}


id: GO:1901964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell proliferation involved in outflow tract morphogenesis.","definition_xrefs":["GOC:TermGenie","GOC:dph","PMID:21419760","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell proliferation involved in outflow tract morphogenesis","termid":"GO:1901963"},{"relation_name":"is_a","term_name":"positive regulation of cell proliferation involved in heart morphogenesis","termid":"GO:2000138"},{"relation_name":"positively_regulates","term_name":"cell proliferation involved in outflow tract morphogenesis","termid":"GO:0061325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cell proliferation involved in outflow tract morphogenesis","synonyms":[{"name":"activation of cell proliferation involved in outflow tract morphogenesis","type":"narrow"},{"name":"up regulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"},{"name":"up-regulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"},{"name":"upregulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"}],"termid":"GO:1901964"}


id: MONDO:0015233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Caudal appendage-deafness syndrome is characterized by caudal appendage, short terminal phalanges, deafness, cryptorchidism, intellectual deficit, short stature and dysmorphism. It has been described in monozygotic twin boys.","definition_xrefs":["Orphanet:1123"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caudal appendage-deafness syndrome","secondary_identifiers":["UMLS:C2931593","GARD:1163","MEDGEN:419843","SCTID:726621009","MESH:C537713"],"synonyms":[{"name":"Lynch Lee Murday syndrome","type":"related"},{"name":"Lynch-Lee-Murday syndrome","type":"exact"},{"name":"caudal appendage deafness","type":"related"},{"name":"caudal appendage, short terminal phalanges, deafness, cryptorchidism and intellectual disability","type":"related"},{"name":"caudal appendage, short terminal phalanges, deafness, cryptorchidism and mental retardation","type":"related"}],"termid":"MONDO:0015233","xrefs":{"Monarch":{"xref_id":"0015233"}}}


id: PBO:0069712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 992, pseudogene","termid":"PBO:0069712"}


id: MONDO:0021089
data:
  {"annotated_genes":["SJAG_01895","SJAG_00260","SJAG_01671"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86549],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[85162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[85371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"}]},"cv_name":"mondo","definition":"Malignant growth of cells in the peripheral nervous system (PNS)or Autonomic Nervous System (ANS), without specification as to location","definition_xrefs":["NCIT:C4961"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral nervous system neoplasm","termid":"MONDO:0001406"},{"relation_name":"is_a","term_name":"nervous system cancer","termid":"MONDO:0005872"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_01671":null,"SJAG_01895":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"peripheral nervous system cancer","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0751428","ICD9:171.9","MEDGEN:155556","SCTID:254986007"],"synonyms":[{"name":"cancer of peripheral nervous system","type":"exact"},{"name":"malignant PNS neoplasm","type":"exact"},{"name":"malignant PNS tumor","type":"exact"},{"name":"malignant PNS tumour","type":"exact"},{"name":"malignant neoplasm of PNS","type":"exact"},{"name":"malignant neoplasm of peripheral nerve","type":"exact"},{"name":"malignant neoplasm of peripheral nervous system","type":"exact"},{"name":"malignant neoplasm of the PNS","type":"exact"},{"name":"malignant neoplasm of the peripheral nerve","type":"exact"},{"name":"malignant neoplasm of the peripheral nervous system","type":"exact"},{"name":"malignant neoplasms, peripheral nerve","type":"exact"},{"name":"malignant peripheral nerve neoplasm","type":"exact"},{"name":"malignant peripheral nerve tumor","type":"exact"},{"name":"malignant peripheral nerve tumour","type":"exact"},{"name":"malignant peripheral nervous system neoplasm","type":"exact"},{"name":"malignant peripheral nervous system tumor","type":"exact"},{"name":"malignant peripheral nervous system tumour","type":"exact"},{"name":"malignant tumor of PNS","type":"exact"},{"name":"malignant tumor of peripheral nerve","type":"exact"},{"name":"malignant tumor of peripheral nervous system","type":"exact"},{"name":"malignant tumor of the PNS","type":"exact"},{"name":"malignant tumor of the peripheral nerve","type":"exact"},{"name":"malignant tumor of the peripheral nervous system","type":"exact"},{"name":"malignant tumour of PNS","type":"exact"},{"name":"malignant tumour of peripheral nerve","type":"exact"},{"name":"malignant tumour of peripheral nervous system","type":"exact"},{"name":"malignant tumour of the PNS","type":"exact"},{"name":"malignant tumour of the peripheral nerve","type":"exact"},{"name":"malignant tumour of the peripheral nervous system","type":"exact"},{"name":"peripheral nervous system cancer","type":"exact"},{"name":"peripheral nervous system neoplasms, malignant","type":"exact"}],"termid":"MONDO:0021089","terms_by_termid":{"MONDO:0007273":null,"MONDO:0011121":null,"MONDO:0013602":null},"xrefs":{"Monarch":{"xref_id":"0021089"}}}


id: MONDO:0042486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary mixed polyposis syndrome","termid":"MONDO:0011023"}],"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":"polyposis syndrome, hereditary mixed, 1","secondary_identifiers":["MEDGEN:331320","OMIM:601228","UMLS:C1832587","DOID:0111685"],"synonyms":[{"name":"HMPS1","type":"related"},{"name":"chromosome 15Q13-q14 Duplication syndrome, 40-Kb","type":"related"},{"name":"colorectal adenoma and carcinoma 1","type":"related"},{"name":"colorectal cancer, susceptibility to, 4","type":"related"},{"name":"colorectal cancer, susceptibility to, on chromosome 15","type":"related"},{"name":"polyposis syndrome, hereditary mixed 1","type":"exact"},{"name":"polyposis syndrome, hereditary mixed, 1","type":"exact"}],"termid":"MONDO:0042486","xrefs":{"Monarch":{"xref_id":"0042486"}}}


id: FYPO:0002548
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 4'-phosphopantothenate measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular 4'-phosphopantothenate level","synonyms":[{"name":"increased 4'-phosphopantothenate accumulation","type":"related"},{"name":"increased cellular 4'-phosphopantothenate level during mitotic cell cycle","type":"related"},{"name":"increased cellular 4'-phosphopantothenate level during vegetative growth","type":"exact"}],"termid":"FYPO:0002548"}


id: PR:Q09801
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pre-mRNA 3'-end-processing factor FIP1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DAN","PANTHER:PTHR13484:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA polyadenylation factor fip1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22G7.10","secondary_identifiers":["UniProtKB:Q09801"],"synonyms":[{"name":"Spom972h-FIP1L1","type":"exact"}],"termid":"PR:Q09801"}


id: GO:0021646
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the vagus nerve. This process pertains to the initial formation of a structure from unspecified parts. This nerve is primarily sensory but also has visceromotor components. It originates in the brain stem and controls many autonomic functions of the heart, lungs, stomach, pharynx, larynx, trachea, esophagus and other gastrointestinal tract components. It controls some motor functions such as speech. The sensory branches mediate sensation from the pharynx, larynx, thorax and abdomen; it also innervates taste buds in the epiglottis.","definition_xrefs":["GOC:dgh","GOC:jid","ISBN:0838580343","GO_REF:0000021","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve formation","termid":"GO:0021603"},{"relation_name":"part_of","term_name":"vagus nerve morphogenesis","termid":"GO:0021644"}],"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":"vagus nerve formation","synonyms":[{"name":"CN X biosynthesis","type":"related"},{"name":"CN X formation","type":"related"}],"termid":"GO:0021646"}


id: PBO:0056399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPRE3 antisense RNA 1","termid":"PBO:0056399"}


id: PBO:0014266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome regulatory particle, lid subcomplex subunit Rpn15/Dss11","termid":"PBO:0014266"}


id: GO:0001764
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The characteristic movement of an immature neuron from germinal zones to specific positions where they will reside as they mature.","definition_xrefs":["GOC:go_curators","CL:0000540"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"generation of neurons","termid":"GO:0048699"}],"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":"neuron migration","secondary_identifiers":["Wikipedia:Neuron_migration","Wikipedia:Neural_development#Neuron_migration"],"synonyms":[{"name":"neuron chemotaxis","type":"exact"},{"name":"neuron guidance","type":"related"},{"name":"neuronal migration","type":"exact"}],"termid":"GO:0001764"}


id: MONDO:0020469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"48,XYYY syndrome is a rare Y chromosome number anomaly that affects only males and is characterized by mild-moderate developmental delay (especially speech), normal to mild intellectual disability, large, irregular teeth with poor enamel, tall stature and acne. Radioulnar stenosis and clinodactyly have also been associated. Boys generally present normal genitalia, while hypogonadism and infertility is frequently reported in adult males.","definition_xrefs":["Orphanet:99329"],"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":"tetrasomy","termid":"MONDO:0030502"},{"relation_name":"is_a","term_name":"chromosome Y disorder","termid":"MONDO:0700028"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"48,XYYY syndrome","secondary_identifiers":["GARD:11985","MEDGEN:1371767","UMLS:C4518082","SCTID:733625003"],"synonyms":[{"name":"48,XYYY","type":"related"}],"termid":"MONDO:0020469","xrefs":{"Monarch":{"xref_id":"0020469"}}}


id: GO:1905136
data:
  {"annotated_genes":["SJAG_02779"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91569],"is_not":false,"summary":null,"term":"GO:1905136"}]},"cv_name":"biological_process","definition":"The directed movement of dethiobiotin from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:TermGenie","GO_REF:0000075","PMID:12557275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transport","termid":"GO:0015718"},{"relation_name":"is_a","term_name":"amide transport","termid":"GO:0042886"},{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02779":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"dethiobiotin import across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1901690","GO:0044757"],"synonyms":[{"name":"dethiobiotin import","type":"related"},{"name":"dethiobiotin import into cell","type":"exact"}],"termid":"GO:1905136","terms_by_termid":{"GO:1905136":null}}


id: PBO:0040179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartate beta-hydroxylase","termid":"PBO:0040179"}


id: PBO:0028923
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_transcription_during_glucose_starvation","termid":"PBO:0028923"}


id: MONDO:0100125
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A perceptual disorder caused by intoxication with hallucinogen drugs, especially LSD. It is characterized by the recurrence of perceptive disturbances that first develop during intoxication. The contents of the perception and visual imagery range extensively and symptoms may include visual disturbances, hallucinations, and psychoses.","definition_xrefs":["PMID:29547576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"perceptual disorders","termid":"MONDO:0024417"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hallucinogen-persisting perception disorder","secondary_identifiers":["ICD10CM:F16.183"],"synonyms":[{"name":"hallucinogen abuse with hallucinogen persisting perception disorder","type":"narrow"}],"termid":"MONDO:0100125","xrefs":{"Monarch":{"xref_id":"0100125"}}}


id: MONDO:0018854
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. PF may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of PF that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic PF.","definition_xrefs":["Orphanet:49566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purpura fulminans","termid":"MONDO:0000809"},{"relation_name":"is_a","term_name":"thrombotic disease","termid":"MONDO:0000831"}],"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":"acquired purpura fulminans","secondary_identifiers":["GARD:18838","UMLS:C4510896","MESH:D014884","MedDRA:10037556","MEDGEN:1377273","MESH:D055665","SCTID:725157006"],"synonyms":[{"name":"acquired PF","type":"exact"},{"name":"acquired purpura fulminans","type":"exact"}],"termid":"MONDO:0018854","xrefs":{"Monarch":{"xref_id":"0018854"}}}


id: GO:0006112
data:
  {"annotated_genes":["SJAG_01783","SJAG_01089","SJAG_01319","SJAG_03964","SJAG_01970","SJAG_01209","SJAG_02178","SJAG_00132","SJAG_03851","SJAG_00570","SJAG_06309","SJAG_00115","SJAG_04067","SJAG_02076","SJAG_01080","SJAG_00963","SJAG_01376","SJAG_01561","SJAG_03442","SJAG_04963"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88615,95293,106141,106373,106374,111237,113957,115295],"is_not":false,"summary":null,"term":"GO:0006112"},{"annotations":[108359],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005978"},{"annotations":[102787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005980"},{"annotations":[113885,117924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005977"},{"annotations":[89596,108109,109231,99775,97105,98109],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061723"},{"annotations":[78413,90445],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0045719"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways by which a cell derives energy from stored compounds such as fats or glycogen.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"energy derivation by oxidation of organic compounds","termid":"GO:0015980"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00115":null,"SJAG_00132":null,"SJAG_00570":null,"SJAG_00963":null,"SJAG_01080":null,"SJAG_01089":null,"SJAG_01209":null,"SJAG_01319":null,"SJAG_01376":null,"SJAG_01561":null,"SJAG_01783":null,"SJAG_01970":null,"SJAG_02076":null,"SJAG_02178":null,"SJAG_03442":null,"SJAG_03851":null,"SJAG_03964":null,"SJAG_04067":null,"SJAG_04963":null,"SJAG_06309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"energy reserve metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"energy reserve metabolism","type":"exact"}],"termid":"GO:0006112","terms_by_termid":{"GO:0005977":null,"GO:0005978":null,"GO:0005980":null,"GO:0006112":null,"GO:0045719":null,"GO:0061723":null}}


id: GO:0110025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The 5' to 3' exonucleolytic resection of DNA at the site of a stalled replication fork that contributes to replication fork processing.","definition_xrefs":["GOC:mah","PMID:28475874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolic process","termid":"GO:0006259"},{"relation_name":"part_of","term_name":"replication fork processing","termid":"GO:0031297"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006260"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0006260"],"is_obsolete":false,"name":"DNA strand resection involved in replication fork processing","termid":"GO:0110025"}


id: MONDO:0030674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Teebi hypertelorism syndrome","termid":"MONDO:0030639"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Teebi hypertelorism syndrome 2","secondary_identifiers":["MEDGEN:1809276","OMIM:619736","UMLS:C5676911","DOID:0081074"],"synonyms":[{"name":"TBHS2","type":"exact"},{"name":"Teebi hypertelorism syndrome 2","type":"exact"}],"termid":"MONDO:0030674","xrefs":{"Monarch":{"xref_id":"0030674"}}}


id: PBO:0001700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin family protein, human UBTD1 homolog","termid":"PBO:0001700"}


id: GO:0006488
data:
  {"annotated_genes":["SJAG_03656","SJAG_04954","SJAG_04363","SJAG_02102","SJAG_03311","SJAG_04952","SJAG_00747","SJAG_03056","SJAG_00924","SJAG_00437","SJAG_01950","SJAG_03764","SJAG_00394","SJAG_00334","SJAG_03774","SJAG_04821"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61218,89886,90636,93400,97847,97897,98185,99283,99486,101788,103056,104471,108749,110536,112000,116182],"is_not":false,"summary":null,"term":"GO:0006488"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dolichol-linked oligosaccharide, usually by a stepwise addition of glycosyl chains to endoplasmic reticulum membrane-bound dolichol-P.","definition_xrefs":["GOC:jl","ISBN:0471331309"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate derivative biosynthetic process","termid":"GO:1901137"},{"relation_name":"part_of","term_name":"protein N-linked glycosylation via asparagine","termid":"GO:0018279"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00334":null,"SJAG_00394":null,"SJAG_00437":null,"SJAG_00747":null,"SJAG_00924":null,"SJAG_01950":null,"SJAG_02102":null,"SJAG_03056":null,"SJAG_03311":null,"SJAG_03656":null,"SJAG_03764":null,"SJAG_03774":null,"SJAG_04363":null,"SJAG_04821":null,"SJAG_04952":null,"SJAG_04954":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006486"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006486","GO:0008150"],"is_obsolete":false,"name":"dolichol-linked oligosaccharide biosynthetic process","references_by_uniquename":{"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-446193"],"synonyms":[{"name":"N-linked glycan precursor biosynthesis","type":"exact"},{"name":"N-linked glycan precursor biosynthetic process","type":"exact"},{"name":"dolichol-linked oligosaccharide anabolism","type":"exact"},{"name":"dolichol-linked oligosaccharide biosynthesis","type":"exact"},{"name":"dolichol-linked oligosaccharide formation","type":"exact"},{"name":"dolichol-linked oligosaccharide synthesis","type":"exact"},{"name":"oligosaccharide-PP-dolichol assembly","type":"exact"}],"termid":"GO:0006488","terms_by_termid":{"GO:0006488":null}}


id: FYPO:0002510
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 palmitoylation of one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein modification during vegetative growth","termid":"FYPO:0000547"},{"relation_name":"is_a","term_name":"abnormal protein palmitoylation during vegetative growth","termid":"FYPO:0002506"},{"relation_name":"is_a","term_name":"increased protein palmitoylation","termid":"FYPO:0002509"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0002494","FYPO:0001320","FYPO:0002274","FYPO:0005447"],"is_obsolete":false,"name":"increased protein palmitoylation during vegetative growth","synonyms":[{"name":"increased protein palmitoylation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002510"}


id: PBO:0054932
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 2346","termid":"PBO:0054932"}


id: PBO:0059719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO2 pseudogene 27","termid":"PBO:0059719"}


id: GO:0008181
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete tumor suppressor (obsolete GO:0008181)","synonyms":[{"name":"tumor suppressor","type":"exact"}],"termid":"GO:0008181"}


id: GO:0019659
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The anaerobic enzymatic chemical reactions and pathways resulting in the breakdown of glucose to lactate, and possibly ethanol, yielding energy in the form of adenosine triphosphate (ATP).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucose catabolic process","termid":"GO:0006007"},{"relation_name":"is_a","term_name":"lactate metabolic process","termid":"GO:0006089"},{"relation_name":"is_a","term_name":"fermentation","termid":"GO:0006113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006091","GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"glucose catabolic process to lactate","secondary_identifiers":["Wikipedia:Lactic_acid_fermentation"],"synonyms":[{"name":"glucose fermentation to lactate","type":"exact"},{"name":"lactate fermentation","type":"exact"}],"termid":"GO:0019659"}


id: GO:0030108
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a MHC class I molecule of the HLA-A subclass to mediate signaling that activates a lymphocyte.","definition_xrefs":["PMID:11929129","GOC:mah","PMID:9368779","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activating MHC class I receptor activity","termid":"GO:0032397"}],"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":"HLA-A specific activating MHC class I receptor activity","termid":"GO:0030108"}


id: PBO:0081633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF561 antisense RNA 1 (head to head)","termid":"PBO:0081633"}


id: GO:0005332
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: gamma-aminobutyric acid(out) + Na+(out) + Cl-(out) = gamma-aminobutyric acid(in) + Na+(in) + Cl(in).","definition_xrefs":["PMID:7589472","PMID:7861179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid:sodium symporter activity","termid":"GO:0005283"},{"relation_name":"is_a","term_name":"gamma-aminobutyric acid transmembrane transporter activity","termid":"GO:0015185"},{"relation_name":"is_a","term_name":"sodium:chloride symporter activity","termid":"GO:0015378"},{"relation_name":"is_a","term_name":"monocarboxylate:sodium symporter activity","termid":"GO:0140161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"gamma-aminobutyric acid:sodium:chloride symporter activity","secondary_identifiers":["Reactome:R-HSA-444007","TC:2.A.22.3.2"],"synonyms":[{"name":"4-aminobutanoate:sodium symporter activity","type":"exact"},{"name":"4-aminobutyrate:sodium symporter activity","type":"exact"},{"name":"GABA:sodium symporter activity","type":"exact"},{"name":"betaine/GABA:sodium symporter activity","type":"exact"},{"name":"gamma-aminobutyric acid:sodium symporter activity","type":"exact"},{"name":"sodium/chloride-dependent GABA transporter activity","type":"broad"}],"termid":"GO:0005332"}


id: PBO:0061170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear-encoded mitochondrial tRNA-Gln (CTG) 1-1","termid":"PBO:0061170"}


id: PBO:0113190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lysolipid acyltransferase; involved in the synthesis of phosphatidic acid from 1-acyl-2-hydroxy-sn-glycero-3-phosphate using oleoyl-CoA as acyl donor and in phospholipid remodeling, incorporating palmitic acid into the sn-1 position of phosphatidylserine and phosphatidylethanolamine; localizes to ER membranes associated with mitochondria (MAMs); contains three predicted transmembrane domains; similar to C. elegans F55A11.5 and maize 1-acyl-glycerol-3-phosphate acyltransferase","termid":"PBO:0113190"}


id: GO:1904971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of viral translation.","definition_xrefs":["GOC:TermGenie","GOC:bhm","GO_REF:0000058","PMID:19666601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of viral process","termid":"GO:0050792"},{"relation_name":"regulates","term_name":"viral translation","termid":"GO:0019081"}],"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 viral translation","synonyms":[{"name":"regulation of viral protein anabolism","type":"exact"},{"name":"regulation of viral protein biosynthesis","type":"exact"},{"name":"regulation of viral protein biosynthetic process","type":"exact"},{"name":"regulation of viral protein formation","type":"exact"},{"name":"regulation of viral protein synthesis","type":"exact"}],"termid":"GO:1904971"}


id: PBO:0026705
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_tryptophan_level","termid":"PBO:0026705"}


id: GO:0030204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving chondroitin sulfate, any member of a group of 10-60 kDa glycosaminoglycans, widely distributed in cartilage and other mammalian connective tissues, the repeat units of which consist of beta-(1,4)-linked D-glucuronyl beta-(1,3)-N-acetyl-D-galactosamine sulfate. They usually occur linked to a protein to form proteoglycans. Two subgroups exist, one in which the sulfate is on the 4-position (chondroitin sulfate A) and the second in which it is in the 6-position (chondroitin sulfate C). They often are polydisperse and often differ in the degree of sulfation from tissue to tissue. The chains of repeating disaccharide are covalently linked to the side chains of serine residues in the polypeptide backbone of a protein by a glycosidic attachment through the trisaccharide unit galactosyl-galactosyl-xylosyl. Chondroitin sulfate B is more usually known as dermatan sulfate.","definition_xrefs":["ISBN:0198506732","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"mucopolysaccharide metabolic process","termid":"GO:1903510"},{"relation_name":"part_of","term_name":"chondroitin sulfate proteoglycan metabolic process","termid":"GO:0050654"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0006790","GO:0008150"],"is_obsolete":false,"name":"chondroitin sulfate metabolic process","secondary_identifiers":["Reactome:R-HSA-1793185"],"synonyms":[{"name":"chondroitin sulfate metabolism","type":"exact"},{"name":"chondroitin sulphate metabolic process","type":"exact"},{"name":"chondroitin sulphate metabolism","type":"exact"}],"termid":"GO:0030204"}


id: PBO:0004499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF2A (predicted)","termid":"PBO:0004499"}


id: PBO:0038569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin binding LIM protein family member 3","termid":"PBO:0038569"}


id: PBO:0054936
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 2350","termid":"PBO:0054936"}


id: GO:0061100
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a neuroendocrine cell of the lung epithelium.","definition_xrefs":["PMID:9126746","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroendocrine cell differentiation","termid":"GO:0061101"},{"relation_name":"is_a","term_name":"lung secretory cell differentiation","termid":"GO:0061140"}],"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":"lung neuroendocrine cell differentiation","termid":"GO:0061100"}


id: MONDO:0007369
data:
  {"annotated_genes":["SJAG_04944"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85398],"is_not":false,"summary":null,"term":"MONDO:0007369"}]},"cv_name":"mondo","definition":"A form of acute hepatic porphyria characterized by the occurrence of neuro-visceral attacks and, more rarely, by the presence of cutaneous lesions.","definition_xrefs":["Orphanet:79273"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hepatic porphyria","termid":"MONDO:0002520"},{"relation_name":"is_a","term_name":"CPOX-related hereditary coproporphyria","termid":"MONDO:0800180"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04944":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0019142"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005066","MONDO:0005093","MONDO:0002515","MONDO:0019142"],"is_obsolete":false,"name":"hereditary coproporphyria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:7425008","UMLS:C0162531","MedDRA:10019866","MESH:D046349","GARD:6619","MEDGEN:57931","DOID:13269","NORD:1228","icd11.foundation:1365918274","NCIT:C84759","NANDO:1200813","NANDO:2201264","OMIM:121300"],"synonyms":[{"name":"CPRO deficiency","type":"related"},{"name":"Cpo deficiency","type":"related"},{"name":"Cpox deficiency","type":"related"},{"name":"Cpx deficiency","type":"related"},{"name":"HCP","type":"related"},{"name":"Harderoporphyria","type":"related"},{"name":"coproporphyria","type":"related"},{"name":"coproporphyria hereditary","type":"related"},{"name":"coproporphyria, hereditary","type":"related"},{"name":"coproporphyrinogen oxidase deficiency","type":"exact"},{"name":"hereditary coproporphyria","type":"exact"},{"name":"hereditary coproporphyria porphyria","type":"exact"},{"name":"porphyria hepatica II","type":"related"},{"name":"porphyria hepatica coproporphyria","type":"related"}],"termid":"MONDO:0007369","terms_by_termid":{"MONDO:0007369":null},"xrefs":{"Monarch":{"xref_id":"0007369"}}}


id: MONDO:0971000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 93","secondary_identifiers":["OMIM:620849","DOID:0070592"],"termid":"MONDO:0971000","xrefs":{"Monarch":{"xref_id":"0971000"}}}


id: GO:0016867
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of an acyl group from one position to another within a single molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"intramolecular acyltransferase activity","secondary_identifiers":["EC:5.4.1.-"],"synonyms":[{"name":"intramolecular transferase activity, transferring acyl groups","type":"exact"}],"termid":"GO:0016867"}


id: PBO:0078889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gln (anticodon CTG) 2-1","termid":"PBO:0078889"}


id: PBO:0045926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EGF containing fibulin extracellular matrix protein 2","termid":"PBO:0045926"}


id: PATO:0001643
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A size quality inhering in a bearer by virtue of the bearer's having a short, stocky build.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stubby","termid":"PATO:0001643"}


id: MOD:00265
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct between two cysteine residues and the tetrapyrrole compound phycourobilin.","definition_xrefs":["RESID:AA0260","PubMed:8876649","PubMed:3208761","PubMed:3838747","PubMed:3838665"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tetrapyrrole modified residue","termid":"MOD:00700"},{"relation_name":"is_a","term_name":"crosslinked L-cysteine residue","termid":"MOD:02044"}],"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":"phycourobilin-bis-L-cysteine","synonyms":[{"name":"3,18-bis(1-[(R)-2-amino-2-carboxyethyl]sulfanylethyl)-2,7,13,17-tetramethyl-1,19-dioxo-4,5,15,16-tetrahydro-(21H,22H,24H)-bilene-b-8,12-dipropanoic acid","type":"exact"},{"name":"3,18-bis(1-[(R)-2-amino-2-carboxyethyl]sulfanylethyl)-8,12-bis(2-carboxyethyl)-2,7,13,17-tetramethyl-4,5,15,16-tetrahydro-(21H,22H,24H)-bilene-b-1,19(4H,16H)-dione","type":"exact"},{"name":"BINDING Phycourobilin chromophore (covalent; via 2 links)","type":"exact"},{"name":"PUB","type":"exact"},{"name":"phycourobilin biscysteine adduct","type":"exact"},{"name":"phycourobilin-bis-L-cysteine","type":"exact"}],"termid":"MOD:00265"}


id: GO:2000399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of thymocyte aggregation.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte cell-cell adhesion","termid":"GO:1903038"},{"relation_name":"is_a","term_name":"regulation of thymocyte aggregation","termid":"GO:2000398"},{"relation_name":"negatively_regulates","term_name":"thymocyte aggregation","termid":"GO:0071594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of thymocyte aggregation","synonyms":[{"name":"negative regulation of T cell precursor aggregation","type":"exact"},{"name":"negative regulation of immature T cell aggregation","type":"related"},{"name":"negative regulation of immature T-cell aggregation","type":"related"},{"name":"negative regulation of immature T-lymphocyte aggregation","type":"exact"},{"name":"negative regulation of thymic lymphocyte aggregation","type":"exact"}],"termid":"GO:2000399"}


id: GO:0035355
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex containing Toll-like receptor 2 (TLR2) and Toll-like receptor 6 (TLR6).","definition_xrefs":["GOC:add","GOC:signaling","PMID:21481769","PMID:19931471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane signaling receptor complex","termid":"GO:0098802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"Toll-like receptor 2-Toll-like receptor 6 protein complex","secondary_identifiers":["GO:0038126"],"synonyms":[{"name":"TLR2-TLR6 protein complex","type":"exact"},{"name":"TLR2:TLR6 heterodimer","type":"exact"},{"name":"TLR6:TLR2 complex","type":"exact"},{"name":"toll-like receptor TLR6:TLR2 heterodimeric complex","type":"exact"}],"termid":"GO:0035355"}


id: MONDO:0019840
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acro-pectoro-renal field defect is a very rare association of a Poland anomaly, that is characterized by unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal head) and a variable degree of ipsilateral hand anomalies (including symbrachydactyly, brachydactyly, absent thumb and hypoplastic fingers), combined with a genito-urinary anomaly. Associated genito-urinary anomalies reported include renal hypoplasia or agenesis, duplex collecting system, ureteropelvic junction obstruction, hypospadias and undescended testicles.","definition_xrefs":["Orphanet:956"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic breast hypoplasia/aplasia","termid":"MONDO:0015856"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acropectororenal dysplasia","secondary_identifiers":["GARD:511","SCTID:720413004"],"synonyms":[{"name":"acro-pectoro-renal field defect","type":"related"},{"name":"brachydactyly, absent pectoral muscles and agenesis/hypoplasia of kidneys","type":"related"}],"termid":"MONDO:0019840","xrefs":{"Monarch":{"xref_id":"0019840"}}}


id: MONDO:0001504
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by recurrent sexual urges, fantasies, or behaviors involving the use of nonliving objects (the \\\"fetish\\\").","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paraphilic disorder","termid":"MONDO:0000596"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fetishistic disorder","secondary_identifiers":["NCIT:C94353","UMLS:C0015957","MEDGEN:8827","ICD9:302.81","ICD10CM:F65.0","MESH:D005329","SCTID:59174009","DOID:1235"],"synonyms":[{"name":"fetishism","type":"exact"}],"termid":"MONDO:0001504","xrefs":{"Monarch":{"xref_id":"0001504"}}}


id: GO:0035840
data:
  {"annotated_genes":["SJAG_04566","SJAG_01196","SJAG_02916","SJAG_00424","SJAG_02222","SJAG_02838","SJAG_00030","SJAG_00152","SJAG_04058","SJAG_01290","SJAG_04901","SJAG_03119"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88276,88946,91093,96370,98820,102548,104124,105568,112218,113485,113818],"is_not":false,"summary":null,"term":"GO:0035840"},{"annotations":[110211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035842"}]},"cv_name":"cellular_component","definition":"A cell tip which has existed for at least one complete cell cycle, and at which polarized growth occurs. For example, in fission yeast the cell end that existed prior to cell division grows immediately after division, and contains a distinctive complement of proteins including actin cytoskeletal structures.","definition_xrefs":["GOC:expert_jd","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growing cell tip","termid":"GO:0035838"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00030":null,"SJAG_00152":null,"SJAG_00424":null,"SJAG_01196":null,"SJAG_01290":null,"SJAG_02222":null,"SJAG_02838":null,"SJAG_02916":null,"SJAG_03119":null,"SJAG_04058":null,"SJAG_04566":null,"SJAG_04901":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"old growing cell tip","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"old growing cell end","type":"exact"}],"termid":"GO:0035840","terms_by_termid":{"GO:0035840":null,"GO:0035842":null}}


id: GO:0010572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate or frequency of platelet activation. Platelet activation is a series of progressive, overlapping events triggered by exposure of the platelets to subendothelial tissue.","definition_xrefs":["GOC:dph","GOC:sl","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of platelet activation","termid":"GO:0010543"},{"relation_name":"is_a","term_name":"positive regulation of cell activation","termid":"GO:0050867"},{"relation_name":"positively_regulates","term_name":"platelet activation","termid":"GO:0030168"}],"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 platelet activation","termid":"GO:0010572"}


id: PBO:0078630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif family like 1","termid":"PBO:0078630"}


id: PBO:0004860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribokinase (predicted)","termid":"PBO:0004860"}


id: PBO:0038932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor V1","termid":"PBO:0038932"}


id: PBO:0088552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gpl1-Gih35-Wdr83 complex WD repeat subunit Wdr83","termid":"PBO:0088552"}


id: GO:0031731
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a CCR6 chemokine receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CCR chemokine receptor binding","termid":"GO:0048020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"CCR6 chemokine receptor binding","synonyms":[{"name":"CCR6 chemokine receptor ligand","type":"narrow"},{"name":"LARC receptor binding","type":"exact"}],"termid":"GO:0031731"}


id: PR:Q09749
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An adiponectin receptor protein 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03283","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":"ADIPOR-like receptor SPBC12C2.09c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12C2.09c","secondary_identifiers":["UniProtKB:Q09749"],"synonyms":[{"name":"Spom972h-ADIPOR2","type":"exact"}],"termid":"PR:Q09749"}


id: GO:0046279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 3,4-dihydroxybenzoate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catechol-containing compound biosynthetic process","termid":"GO:0009713"},{"relation_name":"is_a","term_name":"3,4-dihydroxybenzoate metabolic process","termid":"GO:0046278"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"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:0008150","GO:0044281"],"is_obsolete":false,"name":"3,4-dihydroxybenzoate biosynthetic process","synonyms":[{"name":"protocatechuate anabolism","type":"exact"},{"name":"protocatechuate biosynthesis","type":"exact"},{"name":"protocatechuate biosynthetic process","type":"exact"},{"name":"protocatechuate formation","type":"exact"},{"name":"protocatechuate synthesis","type":"exact"}],"termid":"GO:0046279"}


id: MONDO:0012321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An Alzheimer's disease that is characterized by an associated with variation in the region 7q36.","definition_xrefs":["DOID:0110043","PMID:16175510"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset autosomal dominant Alzheimer disease","termid":"MONDO:0015140"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"Alzheimer disease 10","secondary_identifiers":["MESH:C566465","OMIM:609636","GARD:16514","UMLS:C1864828","MEDGEN:351228"],"synonyms":[{"name":"AD10","type":"exact"},{"name":"Ad10","type":"related"},{"name":"Alzheimer disease 10","type":"exact"},{"name":"Alzheimer disease familial 10","type":"exact"},{"name":"Alzheimer disease type 10","type":"exact"},{"name":"Alzheimer disease, familial, 10","type":"related"},{"name":"Alzheimer disease-10","type":"exact"},{"name":"Alzheimer's disease 10","type":"exact"},{"name":"Alzheimer's disease type 10","type":"exact"}],"termid":"MONDO:0012321","xrefs":{"Monarch":{"xref_id":"0012321"}}}


id: PR:O13709
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC14C4.01c gene.","definition_xrefs":["UniProtKB:O13709","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 C14C4.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC14C4.01c","synonyms":[{"name":"Spom972h-SPAC14C4.01c","type":"exact"}],"termid":"PR:O13709"}


id: PBO:0075847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSU72 pseudogene 6","termid":"PBO:0075847"}


id: PBO:0071036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 38","termid":"PBO:0071036"}


id: GO:0005599
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(X) chains; type X collagen triple helices form hexagonal networks (sheets).","definition_xrefs":["PMID:21421911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"short-chain collagen trimer","termid":"GO:0005598"},{"relation_name":"is_a","term_name":"sheet-forming collagen trimer","termid":"GO:0030935"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"collagen type X trimer","termid":"GO:0005599"}


id: PBO:0071084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 86","termid":"PBO:0071084"}


id: PR:O42903
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rud3 gene.","definition_xrefs":["UniProtKB:O42903","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":"GRIP domain-containing protein C119.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC119.12","synonyms":[{"name":"Spom972h-rud3","type":"exact"}],"termid":"PR:O42903"}


id: PBO:0044516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-2-hydroxyglutarate dehydrogenase","termid":"PBO:0044516"}


id: MONDO:1012877
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dilated cardiomyopathy that occurs in dogs due to a mutation in the RBM20 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dilated cardiomyopathy, dog","termid":"MONDO:1010448"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dilated cardiomyopathy, RBM20-related, dog","secondary_identifiers":["OMIA:002365-9615"],"synonyms":[{"name":"cardiomyopathy, dilated, RBM20-related, dog","type":"related"}],"termid":"MONDO:1012877","xrefs":{"Monarch":{"xref_id":"1012877"}}}


id: PBO:0070770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12","termid":"PBO:0070770"}


id: PBO:0083979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glucosyl hydrolase required for beta-1,6-glucan biosynthesis; type II integral membrane protein that localizes to ER, plasma membrane, sites of polarized growth and secretory vesicles; functionally redundant with Skn1p; KRE6 has a paralog, SKN1, that arose from the whole genome duplication","termid":"PBO:0083979"}


id: GO:0044094
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any constituent part of a host cell's nucleus, a membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. The host is the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host intracellular part","termid":"GO:0033646"},{"relation_name":"part_of","term_name":"host cell nucleus","termid":"GO:0042025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell nuclear part","termid":"GO:0044094"}


id: GO:1903238
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of leukocyte tethering or rolling.","definition_xrefs":["GOC:TermGenie","PMID:18308860","GOC:als","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte tethering or rolling","termid":"GO:1903236"},{"relation_name":"is_a","term_name":"positive regulation of leukocyte adhesion to vascular endothelial cell","termid":"GO:1904996"},{"relation_name":"positively_regulates","term_name":"leukocyte tethering or rolling","termid":"GO:0050901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"positive regulation of leukocyte tethering or rolling","synonyms":[{"name":"activation of leukocyte tethering or rolling","type":"narrow"},{"name":"up regulation of leukocyte tethering or rolling","type":"exact"},{"name":"up-regulation of leukocyte tethering or rolling","type":"exact"},{"name":"upregulation of leukocyte tethering or rolling","type":"exact"}],"termid":"GO:1903238"}


id: PBO:0083854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Exosome non-catalytic core component; involved in 3'-5' RNA processing and degradation in both the nucleus and the cytoplasm; predicted to contain RNA binding domains; mutations in the human ortholog, EXOSC2, cause SHRF (Short stature, Hearing loss, Retinitis pigmentosa and distinctive Facies) syndrome, an RNA exosomopathy","termid":"PBO:0083854"}


id: MONDO:0000314
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary bacterial infectious disease","secondary_identifiers":["DOID:0050338"],"termid":"MONDO:0000314","xrefs":{"Monarch":{"xref_id":"0000314"}}}


id: PBO:0082354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP sulfurylase; catalyzes the primary step of intracellular sulfate activation, essential for assimilatory reduction of sulfate to sulfide, involved in methionine metabolism; human homolog PAPSS2 complements yeast null mutant","termid":"PBO:0082354"}


id: GO:1903512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving phytanic acid.","definition_xrefs":["GOC:dph","GO_REF:0000068","PMID:16799769","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid metabolic process","termid":"GO:0001676"},{"relation_name":"is_a","term_name":"methyl-branched fatty acid metabolic process","termid":"GO:0097089"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"phytanic acid metabolic process","synonyms":[{"name":"phytanic acid metabolism","type":"exact"}],"termid":"GO:1903512"}


id: SO:0002297
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The possible discontinous stretch of DNA that encompass all the TFRSs that regulate a promoter.","definition_xrefs":["PMID:32665585","Bacterial_regulation_working_group:CMA"],"direct_ancestors":[{"relation_name":"has_part","term_name":"transcription_factor_regulatory_site","termid":"SO:0002295"},{"relation_name":"is_a","term_name":"transcriptional_cis_regulatory_region","termid":"SO:0001055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFRS_collection","synonyms":[{"name":"TFRS collection","type":"exact"},{"name":"transcription factor regulatory site collection","type":"exact"}],"termid":"SO:0002297"}


id: GO:2000560
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of CD24 biosynthetic process.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of glycoprotein biosynthetic process","termid":"GO:0010560"},{"relation_name":"is_a","term_name":"regulation of CD24 production","termid":"GO:2000559"},{"relation_name":"positively_regulates","term_name":"CD24 biosynthetic process","termid":"GO:0035724"}],"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 CD24 production","synonyms":[{"name":"positive regulation of CD24 anabolism","type":"exact"},{"name":"positive regulation of CD24 biosynthesis","type":"exact"},{"name":"positive regulation of CD24 biosynthetic process","type":"exact"},{"name":"positive regulation of CD24 formation","type":"exact"},{"name":"positive regulation of CD24 synthesis","type":"exact"}],"termid":"GO:2000560"}


id: PBO:0045556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 8","termid":"PBO:0045556"}


id: FYPO:0004883
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the mitotic spindle midzone is abnormal. The mitotic spindle midzone is the area in the center of the mitotic spindle where the spindle microtubules from opposite poles overlap.","definition_xrefs":["GO:1990023","GO:1902967","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to mitotic spindle","termid":"FYPO:0002824"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization to mitotic spindle midzone","synonyms":[{"name":"abnormal protein localisation to mitotic spindle midzone","type":"exact"},{"name":"abnormal protein localization to spindle midzone during mitotic cell cycle","type":"related"},{"name":"abnormal protein localization to spindle midzone during vegetative growth","type":"exact"}],"termid":"FYPO:0004883"}


id: PBO:0113370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with NADP(H) oxidoreductase activity; transcription is regulated by Stb5p in response to NADPH depletion induced by diamide; promoter contains an Stb5p binding site and Stb5p binding is enriched at the promoter; negative regulator of nonselective autophagy; protein abundance increases in response to DNA replication stress","termid":"PBO:0113370"}


id: PBO:0089866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIA machinery CIA1/CFD1 fusion protein","termid":"PBO:0089866"}


id: MONDO:0002222
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the urethra. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"benign urethral neoplasm","termid":"MONDO:0004177"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urethra leiomyoma","secondary_identifiers":["MEDGEN:237035","UMLS:C1336888","DOID:2142","NCIT:C6171"],"synonyms":[{"name":"leiomyoma of the urethra","type":"exact"},{"name":"leiomyoma of urethra","type":"exact"},{"name":"urethra leiomyoma","type":"exact"},{"name":"urethral leiomyoma","type":"exact"}],"termid":"MONDO:0002222","xrefs":{"Monarch":{"xref_id":"0002222"}}}


id: GO:0070358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process involved in the controlled movement of a bacterial cell powered by the continuous polymerization of actin at one pole of the cell.","definition_xrefs":["PMID:15773977","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell motility","termid":"GO:0048870"}],"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":"actin polymerization-dependent cell motility","synonyms":[{"name":"cell motility by actin tail formation","type":"exact"}],"termid":"GO:0070358"}


id: GO:0015593
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of allose from one side of a membrane to the other. Allose is an aldohexose similar to glucose, differing only in the configuration of the hydroxyl group of C-3.","definition_xrefs":["GOC:mtg_transport","GOC:ai","ISBN:0815340729"],"gene_count":0,"genotype_count":0,"name":"obsolete allose transmembrane transporter activity (obsolete GO:0015593)","termid":"GO:0015593"}


id: PBO:0048834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein nucleolar 2","termid":"PBO:0048834"}


id: GO:0036366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The release of transforming growth factor beta 3 (TGF-beta3) from its latent state.","definition_xrefs":["PMID:12482908","PMID:9170210","GOC:sl"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta3 activation (obsolete GO:0036366)","synonyms":[{"name":"TGF-beta 3 activation","type":"exact"},{"name":"TGFB3 activation","type":"exact"},{"name":"TGFbeta 3 activation","type":"exact"}],"termid":"GO:0036366"}


id: PBO:0055780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LON peptidase N-terminal domain and ring finger 2","termid":"PBO:0055780"}


id: FYPO:0007841
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of peptide alpha-N-acetyltransferase activity is decreased.","definition_xrefs":["PomBase:mah","PMID:34019809"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal peptide alpha-N-acetyltransferase activity","termid":"FYPO:0007839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000661","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"decreased peptide alpha-N-acetyltransferase activity","synonyms":[{"name":"decreased NAT activity","type":"related"},{"name":"decreased protein N-terminal acetyltransferase activity","type":"exact"},{"name":"reduced peptide alpha-N-acetyltransferase activity","type":"exact"}],"termid":"FYPO:0007841"}


id: PBO:0087240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine kinase involved in cell cycle regulation and rDNA integrity; associated with late pre-40S particles via its conserved C-terminal domain; prevents premature use of pre-40S particles in translation; association with pre-40S particles regulated by its catalytic ATPase site and likely occurs after the release of Rio2p from these particles; involved in cell cycle progression and processing of the 20S pre-rRNA into mature 18S rRNA; phosphorylates Rpa43p in anaphase to remove Pol I from rDNA","termid":"PBO:0087240"}


id: PBO:0034085
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-disposition_of","termid":"PBO:0034085"}


id: PBO:0053557
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 564","termid":"PBO:0053557"}


id: GO:0097351
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a toxin to prevent it from interacting with other partners or to inhibit its localization to the area of the cell or complex where it is active.","definition_xrefs":["PMID:21819231","GOC:rs","PMID:22545240","PMID:19143615","PMID:19325885","Wikipedia:Toxin-antitoxin_system#Type_II","PMID:24806488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular sequestering activity","termid":"GO:0140313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140313"}],"interesting_parent_ids":["GO:0140313","GO:0003674"],"is_obsolete":false,"name":"toxin sequestering activity","synonyms":[{"name":"toxin-antitoxin pair type I binding","type":"narrow"},{"name":"toxin-antitoxin pair type II binding","type":"narrow"}],"termid":"GO:0097351"}


id: PBO:0004386
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"after human IQWD1","termid":"PBO:0004386"}


id: GO:0140870
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of RNA polymerase.","definition_xrefs":["PMID:18313387","PMID:15300239","PMID:31048766"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0140678","GO:0004857","GO:0098772"],"is_obsolete":false,"name":"RNA polymerase inhibitor activity","termid":"GO:0140870"}


id: PBO:0049288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase alpha 7, pseudogene","termid":"PBO:0049288"}


id: MONDO:0005188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Kaposi sarcoma that develops after organ transplantation or immunosuppressive treatment.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kaposi's sarcoma","termid":"MONDO:0005055"},{"relation_name":"is_a","term_name":"nosocomial infection","termid":"MONDO:0043544"}],"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":"iatrogenic Kaposi's sarcoma","secondary_identifiers":["NCIT:C35873","MEDGEN:235203","UMLS:C1334149"],"synonyms":[{"name":"iatrogenic Kaposi sarcoma","type":"exact"},{"name":"iatrogenic Kaposi's sarcoma","type":"exact"}],"termid":"MONDO:0005188","xrefs":{"Monarch":{"xref_id":"0005188"}}}


id: SO:0002337
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Cytosolic 2S rRNA is a 30 nucleotide RNA component of the large subunit of cytosolic ribosomes in Drosophila and at least some other Diptera. It is homologous to the 3' part of other 5.8S rRNA molecules. The 3' end of the 5.8S molecule is able to base-pair with the 5' end of the 2S rRNA to generate a helical region equivalent in position to the 'GC-rich hairpin' found in all previously sequenced 5.8S molecules.","definition_xrefs":["PMID:10788608","PMID:407103","PMID:768488","PMID:4847940"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"cytosolic_rRNA_2S_gene","termid":"SO:0002336"},{"relation_name":"is_a","term_name":"cytosolic_LSU_rRNA","termid":"SO:0000651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic_2S_rRNA","synonyms":[{"name":"cytosolic 2S rRNA","type":"exact"},{"name":"cytosolic rRNA 2S","type":"exact"}],"termid":"SO:0002337"}


id: PBO:0043710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COX6A1 pseudogene 7","termid":"PBO:0043710"}


id: PBO:0055900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 23","termid":"PBO:0055900"}


id: GO:0009176
data:
  {"annotated_genes":["SJAG_03771","SJAG_04487","SJAG_04627"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88889,107839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006231"},{"annotations":[98491,107840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006226"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving pyrimidine deoxynucleoside monophosphate, a compound consisting of a pyrimidine base linked to a deoxyribose sugar esterified with phosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside monophosphate metabolic process","termid":"GO:0009129"},{"relation_name":"is_a","term_name":"deoxyribonucleoside monophosphate metabolic process","termid":"GO:0009162"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03771":null,"SJAG_04487":null,"SJAG_04627":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"pyrimidine deoxyribonucleoside monophosphate metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pyrimidine deoxyribonucleoside monophosphate metabolism","type":"exact"}],"termid":"GO:0009176","terms_by_termid":{"GO:0006226":null,"GO:0006231":null}}


id: FYPO:0001135
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 the 35S rRNA primary transcript measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased rRNA precursor level","termid":"FYPO:0003600"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0006551","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased 35S rRNA precursor level","synonyms":[{"name":"increased 35S rRNA precursor accumulation","type":"related"},{"name":"increased 35S rRNA precursor level during mitotic cell cycle","type":"related"},{"name":"increased 35S rRNA precursor level during vegetative growth","type":"exact"},{"name":"increased 35S rRNA precursor transcript level","type":"exact"},{"name":"increased 35S rRNA primary transcript level","type":"exact"}],"termid":"FYPO:0001135"}


id: GO:0102172
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4alpha-hydroxymethyl,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-ergost-24(241)-en-3beta-ol + NADH + O2 + H+ = 4alpha-formyl,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-ergost-24(241)-en-3beta-ol + NAD + 2 H2O.","definition_xrefs":["RHEA:58860","GOC:pz"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"4alpha-hydroxymethyl,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-ergost-24(241)-en-3beta-ol-4alpha-methyl oxidase activity","secondary_identifiers":["MetaCyc:RXN-11925"],"termid":"GO:0102172"}


id: MONDO:1012213
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"persistent right aortic arch, non-human animal","termid":"MONDO:1011644"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent right aortic arch, domestic cat","secondary_identifiers":["OMIA:000794-9685"],"termid":"MONDO:1012213","xrefs":{"Monarch":{"xref_id":"1012213"}}}


id: PBO:0090301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA methyltransferase Rrp8","termid":"PBO:0090301"}


id: MONDO:0018191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tumor of testis and paratestis (obsolete MONDO:0018191)","secondary_identifiers":["Orphanet:363472"],"synonyms":[{"name":"testicular and paratesticular tumor","type":"exact"},{"name":"testicular and paratesticular tumour","type":"exact"}],"termid":"MONDO:0018191","xrefs":{"Monarch":{"xref_id":"0018191"}}}


id: GO:1905804
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 manganese ion.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:23721876"],"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 stimulus","termid":"GO:0048584"},{"relation_name":"is_a","term_name":"regulation of cellular response to manganese ion","termid":"GO:1905802"},{"relation_name":"positively_regulates","term_name":"cellular response to manganese ion","termid":"GO:0071287"}],"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 manganese ion","synonyms":[{"name":"activation of cellular response to manganese","type":"narrow"},{"name":"activation of cellular response to manganese ion","type":"narrow"},{"name":"positive regulation of cellular response to manganese","type":"exact"},{"name":"up regulation of cellular response to manganese","type":"exact"},{"name":"up regulation of cellular response to manganese ion","type":"exact"},{"name":"up-regulation of cellular response to manganese","type":"exact"},{"name":"up-regulation of cellular response to manganese ion","type":"exact"},{"name":"upregulation of cellular response to manganese","type":"exact"},{"name":"upregulation of cellular response to manganese ion","type":"exact"}],"termid":"GO:1905804"}


id: GO:0150159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of interleukin-34 production.","definition_xrefs":["GOC:aruk","PMID:26754294"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of interleukin-34 production","termid":"GO:0150157"},{"relation_name":"negatively_regulates","term_name":"interleukin-34 production","termid":"GO:0150155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of interleukin-34 production","secondary_identifiers":["GO:0150162"],"synonyms":[{"name":"negative regulation of interleukin-34 biosynthetic process","type":"narrow"}],"termid":"GO:0150159"}


id: MONDO:0004943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant soft tissue neoplasm that arises from the structures of the orbit. The majority of the cases are rhabdomyosarcomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orbital cancer","termid":"MONDO:0002889"},{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"}],"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":"orbit sarcoma","secondary_identifiers":["UMLS:C1335131","DOID:9987","NCIT:C6095","MEDGEN:277449","SCTID:699354006"],"synonyms":[{"name":"orbit of skull sarcoma","type":"exact"},{"name":"orbital sarcoma","type":"exact"},{"name":"sarcoma of orbit","type":"exact"},{"name":"sarcoma of orbit of skull","type":"exact"},{"name":"sarcoma of the orbit","type":"exact"}],"termid":"MONDO:0004943","xrefs":{"Monarch":{"xref_id":"0004943"}}}


id: GO:0060321
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The recognition and acceptance of pollen by cells in the stigma, mediated by the sharing and interaction of the single locus incompatibility haplotypes.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"recognition of pollen","termid":"GO:0048544"},{"relation_name":"part_of","term_name":"pollen-pistil interaction","termid":"GO:0009875"}],"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":"acceptance of pollen","synonyms":[{"name":"acceptance of non-self pollen","type":"related"},{"name":"acceptance of self pollen","type":"narrow"},{"name":"self-compatibility","type":"related"}],"termid":"GO:0060321"}


id: GO:0060573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process involved in the specification of the identity of a cell in a field of cells that is being instructed as to how to differentiate. Once specification has taken place, that cell will be committed to differentiate down a specific pathway if left in its normal environment.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate specification","termid":"GO:0001708"},{"relation_name":"part_of","term_name":"cell fate commitment involved in pattern specification","termid":"GO:0060581"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell fate specification involved in pattern specification","termid":"GO:0060573"}


id: GO:0017190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The acetylation of the N-terminal aspartic acid of proteins; catalyzed by aspartate N-acetyltransferase.","definition_xrefs":["RESID:AA0042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-terminal protein amino acid acetylation","termid":"GO:0006474"},{"relation_name":"is_a","term_name":"peptidyl-aspartic acid modification","termid":"GO:0018197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0051604"],"is_obsolete":false,"name":"N-terminal peptidyl-aspartic acid acetylation","termid":"GO:0017190"}


id: PBO:0076492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell-interacting, activating receptor on myeloid cells 1","termid":"PBO:0076492"}


id: MONDO:0001284
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Endometriosis that affects the intesines.","direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"},{"relation_name":"is_a","term_name":"endometriosis","termid":"MONDO:0005133"}],"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":"endometriosis of intestine","secondary_identifiers":["SCTID:5562006","icd11.foundation:706777963","ICD9:617.5","MEDGEN:510251","UMLS:C0156347","DOID:11428","ICD10CM:N80.5"],"synonyms":[{"name":"endometriosis (disease) of intestine","type":"exact"},{"name":"intestine endometriosis (disease)","type":"exact"}],"termid":"MONDO:0001284","xrefs":{"Monarch":{"xref_id":"0001284"}}}


id: GO:0016635
data:
  {"annotated_genes":["SJAG_01671","SJAG_02876","SJAG_00260","SJAG_00197"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98003],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106430"},{"annotations":[91853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070819"},{"annotations":[88701,88337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008177"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a CH-CH group acts as a hydrogen or electron donor and reduces a quinone or related compound.","definition_xrefs":["EC:1.3.5.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors","termid":"GO:0016627"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00260":null,"SJAG_01671":null,"SJAG_02876":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0016635","terms_by_termid":{"GO:0008177":null,"GO:0070819":null,"GO:0106430":null}}


id: PR:O94574
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1773.17c gene.","definition_xrefs":["UniProtKB:O94574","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":"2-hydroxyacid dehydrogenase C1773.17c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1773.17c","synonyms":[{"name":"Spom972h-SPBC1773.17c","type":"exact"}],"termid":"PR:O94574"}


id: PBO:0056439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MARK2 pseudogene 12","termid":"PBO:0056439"}


id: PBO:0055588
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 3024","termid":"PBO:0055588"}


id: GO:2000045
data:
  {"annotated_genes":["SJAG_02810","SJAG_03699","SJAG_03048","SJAG_03591","SJAG_01311","SJAG_00996","SJAG_00071","SJAG_01825","SJAG_02723","SJAG_03681","SJAG_05346","SJAG_01210","SJAG_02404","SJAG_01401","SJAG_04140","SJAG_00169","SJAG_00991","SJAG_02026"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91252,105440,116517],"is_not":false,"summary":null,"term":"GO:2000045"},{"annotations":[101848,115346,108346,88458,101111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031568"},{"annotations":[90817,109132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[88459,92831,98377,108347,91248,91668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000134"},{"annotations":[105284,105439,116515,101113,108644,106122,101863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900087"},{"annotations":[101115,110656,114784,115348,91254,108352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007089"}]},"cv_name":"biological_process","definition":"Any signaling pathway that modulates the activity of a cell cycle cyclin-dependent protein kinase to modulate the switch from G1 phase to S phase of the mitotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle phase transition","termid":"GO:1901990"},{"relation_name":"is_a","term_name":"regulation of cell cycle G1/S phase transition","termid":"GO:1902806"},{"relation_name":"regulates","term_name":"G1/S transition of mitotic cell cycle","termid":"GO:0000082"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00169":null,"SJAG_00991":null,"SJAG_00996":null,"SJAG_01210":null,"SJAG_01311":null,"SJAG_01401":null,"SJAG_01825":null,"SJAG_02026":null,"SJAG_02404":null,"SJAG_02723":null,"SJAG_02810":null,"SJAG_03048":null,"SJAG_03591":null,"SJAG_03681":null,"SJAG_03699":null,"SJAG_04140":null,"SJAG_05346":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044772"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0044772"],"is_obsolete":false,"name":"regulation of G1/S transition of mitotic cell cycle","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:2000045","terms_by_termid":{"GO:0007089":null,"GO:0031568":null,"GO:0031571":null,"GO:1900087":null,"GO:2000045":null,"GO:2000134":null}}


id: GO:0140058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a neuron projection are generated and organized into branches. A neuron projection is any process extending from a neural cell, such as axons or dendrites.","definition_xrefs":["PMID:23764288","PMID:17114044","GOC:bc","GOC:aruk","PMID:23270857"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection morphogenesis","termid":"GO:0048812"}],"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":"neuron projection arborization","synonyms":[{"name":"branching morphogenesis of a neurite","type":"related"},{"name":"branching morphogenesis of a neuron projection","type":"related"},{"name":"neurite arborization","type":"exact"},{"name":"neurite branching","type":"exact"},{"name":"neuron projection branching","type":"exact"}],"termid":"GO:0140058"}


id: PR:O14269
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- iss10 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14269"],"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 C7D4.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC7D4.14c","synonyms":[{"name":"Spom972h-iss10","type":"exact"}],"termid":"PR:O14269"}


id: PBO:0078391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Phe (anticodon GAA) 1-6","termid":"PBO:0078391"}


id: PBO:0041983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 27","termid":"PBO:0041983"}


id: GO:0090343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the rate, frequency, or extent of cell aging. Cell aging is the progression of the cell from its inception to the end of its lifespan.","definition_xrefs":["GOC:dph","GOC:BHF","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cell aging (obsolete GO:0090343)","termid":"GO:0090343"}


id: GO:0000783
data:
  {"annotated_genes":["SJAG_01864","SJAG_02362","SJAG_01777","SJAG_04245","SJAG_02194","SJAG_01378","SJAG_03685","SJAG_03092"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104569],"is_not":false,"summary":null,"term":"GO:0000783"},{"annotations":[109822,114052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990879"},{"annotations":[104572,115384,94589,89274,99218,91343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070187"}]},"cv_name":"cellular_component","definition":"A complex of DNA and protein located at the end of a linear chromosome in the nucleus that protects and stabilizes a linear chromosome.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomere cap complex","termid":"GO:0000782"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":8,"genes_by_uniquename":{"SJAG_01378":null,"SJAG_01777":null,"SJAG_01864":null,"SJAG_02194":null,"SJAG_02362":null,"SJAG_03092":null,"SJAG_03685":null,"SJAG_04245":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"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0032991","GO:0005694"],"is_obsolete":false,"name":"nuclear telomere cap complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000783","terms_by_termid":{"GO:0000783":null,"GO:0070187":null,"GO:1990879":null}}


id: GO:0010800
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of peptidyl-threonine phosphorylation. Peptidyl-threonine phosphorylation is the phosphorylation of peptidyl-threonine to form peptidyl-O-phospho-L-threonine.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein phosphorylation","termid":"GO:0001934"},{"relation_name":"is_a","term_name":"regulation of peptidyl-threonine phosphorylation","termid":"GO:0010799"},{"relation_name":"positively_regulates","term_name":"peptidyl-threonine phosphorylation","termid":"GO:0018107"}],"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 peptidyl-threonine phosphorylation","termid":"GO:0010800"}


id: GO:0035062
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A nucleoplasmic speckle distributed in the interchromatin space of cells in close proximity to chromatin. Omega speckles are distinct from interchromatin granules and contain heterogeneous nuclear RNA-binding proteins (hnRNPs).","definition_xrefs":["PMID:10984439","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear speck","termid":"GO:0016607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005654"}],"interesting_parent_ids":["GO:0005654","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"omega speckle","termid":"GO:0035062"}


id: PBO:0113016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bacterially-derived sulfatase; required for use of alkyl sulfates as sulfur source","termid":"PBO:0113016"}


id: MONDO:0005731
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A parasitic infection caused by genus of filarial worms called Dipetalonema. It produces microfilariae in the blood and body fluids.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Rhabditida infectious disease","termid":"MONDO:0005943"},{"relation_name":"is_a","term_name":"filariasis","termid":"MONDO:0016075"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dipetalonemiasis","secondary_identifiers":["UMLS:C0012517","NORD:705","DOID:14422","GARD:4","ICD9:125.4","MEDGEN:4329","NCIT:C34540","MESH:D004154","SCTID:15629006"],"synonyms":[{"name":"Acanthocheilonema perstans infection","type":"related"},{"name":"Acanthocheilonemiasis","type":"related"},{"name":"Dipetalonema infection","type":"exact"},{"name":"Dipetalonema infections","type":"exact"},{"name":"Dipetalonema infectious disease","type":"exact"},{"name":"Mansonella perstans","type":"exact"},{"name":"Mansonella perstans caused disease or disorder","type":"exact"},{"name":"Mansonella perstans disease or disorder","type":"exact"},{"name":"Mansonella perstans infectious disease","type":"exact"},{"name":"dipetalonemiasis","type":"exact"},{"name":"infection by Dipetalonema","type":"exact"},{"name":"infection by Dipetalonema perstans","type":"exact"},{"name":"infection by Dipetalonema perstans (disorder) [ambiguous]","type":"exact"}],"termid":"MONDO:0005731","xrefs":{"Monarch":{"xref_id":"0005731"}}}


id: FYPO:0007570
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 septation initiation network signaling takes place at both mitotic spindle pole bodies. Normally, SIN signaling occurs only at the new SPB.","definition_xrefs":["PMID:15132994","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal septation initiation network signaling","termid":"FYPO:0007569"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000298","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"septation initiation network signaling from both mitotic spindle pole bodies","synonyms":[{"name":"SIN signaling from both mitotic SPBs","type":"exact"},{"name":"SIN signaling from both mitotic spindle pole bodies","type":"exact"},{"name":"abnormal septation initiation network signaling from both mitotic spindle pole bodies","type":"exact"},{"name":"septation initiation network signaling from both mitotic SPBs","type":"exact"},{"name":"septation initiation network signaling from both mitotic spindle pole bodies during mitotic cell cycle","type":"related"},{"name":"septation initiation network signaling from both mitotic spindle pole bodies during vegetative growth","type":"exact"},{"name":"septation initiation network signaling from old and new mitotic SPBs","type":"exact"},{"name":"septation initiation network signaling from old and new mitotic spindle pole bodies","type":"exact"},{"name":"septation initiation network signalling from both mitotic spindle pole bodies","type":"exact"},{"name":"septation initiation signaling from both mitotic spindle pole bodies","type":"exact"}],"termid":"FYPO:0007570"}


id: GO:0019234
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive a fast pain stimulus, convert it to a molecular signal, and recognize and characterize the signal. This is a neurological process. Fast pain is often subjectively described as a sharp or stabbing pain; in humans, the signals from a fast pain stimulus are perceived and relayed along myelinated A-delta fibers to the central nervous system, reaching their target in about 0.1 seconds.","definition_xrefs":["PMID:38704307"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory perception of pain","termid":"GO:0019233"}],"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":"sensory perception of fast pain","termid":"GO:0019234"}


id: MONDO:1012777
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dwarfism that occurs in horses due to a mutation in the B4GALT7 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"dwarfism, non-human animal","termid":"MONDO:1012971"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dwarfism, B4GALT7-related, horse","secondary_identifiers":["OMIA:002068-9796"],"synonyms":[{"name":"dwarfism, Friesian horse","type":"related"}],"termid":"MONDO:1012777","xrefs":{"Monarch":{"xref_id":"1012777"}}}


id: PBO:0043056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroitin polymerizing factor 2","termid":"PBO:0043056"}


id: MONDO:0005134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune demyelinating disease of the central nervous system that is produced experimentally in animals by the injection of homogenized brain or spinal cord in Freund's adjuvant. Myelin basic protein appears to be the antigen that elicits the hypersensitivity immune response which is characterized by focal areas of lymphocyte and macrophage infiltration into the brain, associated with demyelination and destruction of the blood-brain barrier. Experimental allergic encephalomyelitis (EAE) is used as an animal model for demyelinating diseases of the human central nervous system such as multiple sclerosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"encephalomyelitis","termid":"MONDO:0005156"},{"relation_name":"excluded_subClassOf","term_name":"CNS demyelinating autoimmune disease","termid":"MONDO:0006704"},{"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":"experimental autoimmune encephalomyelitis","secondary_identifiers":["EFO:0001066","MESH:D004681"],"termid":"MONDO:0005134","xrefs":{"Monarch":{"xref_id":"0005134"}}}


id: GO:0090514
data:
  {"annotated_genes":["SJAG_03256"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103324],"is_not":false,"summary":null,"term":"GO:0090514"}]},"cv_name":"biological_process","definition":"The directed movement of L-tyrosine into the vacuole across the vacuolar membrane.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tyrosine transport","termid":"GO:0015828"},{"relation_name":"is_a","term_name":"amino acid transmembrane import into vacuole","termid":"GO:0032975"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03256":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"L-tyrosine transmembrane import into vacuole","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0090514","terms_by_termid":{"GO:0090514":null}}


id: PBO:0051201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 4-28","termid":"PBO:0051201"}


id: MONDO:0014257
data:
  {"annotated_genes":["SJAG_00933"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85361],"is_not":false,"summary":null,"term":"MONDO:0014257"}]},"cv_name":"mondo","definition":"Any nephrotic syndrome in which the cause of the disease is a mutation in the COQ8B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial idiopathic steroid-resistant nephrotic syndrome","termid":"MONDO:0019006"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00933":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"nephrotic syndrome, type 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:816295","UMLS:C3809965","DOID:0080391","OMIM:615573","GARD:15989"],"synonyms":[{"name":"COQ8B nephrotic syndrome","type":"exact"},{"name":"NPHS9","type":"related"},{"name":"nephrotic syndrome caused by mutation in COQ8B","type":"exact"},{"name":"nephrotic syndrome, type 9","type":"exact"}],"termid":"MONDO:0014257","terms_by_termid":{"MONDO:0014257":null},"xrefs":{"Monarch":{"xref_id":"0014257"}}}


id: PBO:0074873
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 56","termid":"PBO:0074873"}


id: PBO:0085601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in cell separation during budding; one of two S. cerevisiae homologs (Sds23p and Sds24p) of the S. pombe Sds23 protein, which is implicated in APC/cyclosome regulation; SDS23 has a paralog, SDS24, that arose from the whole genome duplication","termid":"PBO:0085601"}


id: MONDO:0010713
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, hereditary, primary immunodeficiency due to a complement cascade protein anomaly characterized by significantly increased susceptibility to Neisseria species infections. It only affects males, typically presenting with severe or fulminant meningococcal disease.","definition_xrefs":["Orphanet:2966"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"}],"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":"properdin deficiency, X-linked","secondary_identifiers":["MESH:C537241","ICD9:279.8","OMIM:312060","DOID:0111768","UMLS:C1839454","GARD:4513","SCTID:81166004","NANDO:2200789","MEDGEN:333322"],"synonyms":[{"name":"CFPD","type":"related"},{"name":"PFD","type":"related"},{"name":"complement Factor properdin deficiency","type":"related"},{"name":"properdin P Factor deficiency","type":"related"},{"name":"properdin deficiency, X-linked","type":"exact"},{"name":"properdin deficiency, X-linked, X-linked recessive","type":"exact"},{"name":"properdin deficiency, type 1","type":"related"},{"name":"properdin deficiency, type 2","type":"related"},{"name":"properdin deficiency, type 3","type":"related"}],"termid":"MONDO:0010713","xrefs":{"Monarch":{"xref_id":"0010713"}}}


id: PBO:0091897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small non-coding RNA, probably longer, possible ght6 antisense","termid":"PBO:0091897"}


id: PBO:0047404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 42","termid":"PBO:0047404"}


id: GO:0034986
data:
  {"annotated_genes":["SJAG_01418","SJAG_03862"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100067,113323],"is_not":false,"summary":null,"term":"GO:0034986"}]},"cv_name":"molecular_function","definition":"Directly binding to and delivering iron ions to a target protein.","definition_xrefs":["GOC:vk","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metallochaperone activity","termid":"GO:0016530"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01418":null,"SJAG_03862":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140104"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0140104"],"is_obsolete":false,"name":"iron chaperone activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9854405","Reactome:R-HSA-9854984","Reactome:R-HSA-9866272"],"termid":"GO:0034986","terms_by_termid":{"GO:0034986":null}}


id: PR:Q10075
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pcs2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10075"],"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":"glutathione gamma-glutamylcysteinyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3H1.10","synonyms":[{"name":"Spom972h-pcs2","type":"exact"},{"name":"phytochelatin synthase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10075"}


id: FYPO:0004503
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 protein having high molecular mass due to polyubiquitin conjugation is greater than normal.","definition_xrefs":["PMID:16149916","PMID:8247131","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0006551"],"is_obsolete":false,"name":"increased cellular HMW ubiquitin conjugate level","synonyms":[{"name":"accumulation of HMW ubiquitin conjugates","type":"exact"},{"name":"accumulation of high molecular mass ubiquitin conjugates","type":"exact"},{"name":"accumulation of high molecular weight ubiquitin conjugates","type":"exact"},{"name":"increased HMW ubiquitin conjugate accumulation","type":"related"},{"name":"increased cellular HMW ubiquitin conjugate level during mitotic cell cycle","type":"related"},{"name":"increased cellular HMW ubiquitin conjugate level during vegetative growth","type":"exact"},{"name":"increased cellular high molecular mass ubiquitin conjugate level during vegetative growth","type":"exact"},{"name":"increased cellular high molecular weight ubiquitin conjugate level during vegetative growth","type":"exact"}],"termid":"FYPO:0004503"}


id: MONDO:0012664
data:
  {"annotated_genes":["SJAG_16456"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85020],"is_not":false,"summary":null,"term":"MONDO:0012664"}]},"cv_name":"mondo","definition":"Any autosomal recessive spastic ataxia in which the cause of the disease is a mutation in the MARS2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"autosomal recessive spastic ataxia","termid":"MONDO:0017847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"spastic ataxia 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:17425","ICD10CM:G11.4","UMLS:C1969645","OMIM:611390","Orphanet:314603","MEDGEN:370715","DOID:0050942","MESH:C566956"],"synonyms":[{"name":"ARSAL","type":"exact"},{"name":"MARS2 autosomal recessive spastic ataxia","type":"exact"},{"name":"SPAX3","type":"exact"},{"name":"autosomal recessive spastic ataxia caused by mutation in MARS2","type":"exact"},{"name":"autosomal recessive spastic ataxia type 3","type":"exact"},{"name":"autosomal recessive spastic ataxia with leukoencephalopathy","type":"related"},{"name":"spastic ataxia 3, autosomal recessive","type":"related"},{"name":"spastic ataxia type 3","type":"exact"}],"termid":"MONDO:0012664","terms_by_termid":{"MONDO:0012664":null},"xrefs":{"Monarch":{"xref_id":"0012664"}}}


id: GO:0070437
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains Grb2 and the adaptor protein Shc, and is involved in linking epidermal growth factor receptor (EGFR) activation to the p21-Ras pathway.","definition_xrefs":["GOC:mah","PMID:7798267"],"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:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Grb2-Shc complex","synonyms":[{"name":"Grb2-Shc complex, EGF stimulated","type":"narrow"}],"termid":"GO:0070437"}


id: PBO:0074247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC66A2 pseudogene 1","termid":"PBO:0074247"}


id: PBO:0074450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"survival of motor neuron 2, centromeric","termid":"PBO:0074450"}


id: PBO:0058038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4259","termid":"PBO:0058038"}


id: PBO:0034809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smc5-6 complex non-SMC MAGE family subunit Nse3","termid":"PBO:0034809"}


id: MONDO:0017956
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mixed autoinflammatory and autoimmune syndrome (obsolete MONDO:0017956)","secondary_identifiers":["Orphanet:324933"],"termid":"MONDO:0017956","xrefs":{"Monarch":{"xref_id":"0017956"}}}


id: GO:0103037
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sn-glycerol 3-phosphate + NADP = H+ + L-glyceraldehyde 3-phosphate + NADPH.","definition_xrefs":["GOC:pz","PMID:18620424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"L-glyceraldehyde 3-phosphate reductase activity","secondary_identifiers":["MetaCyc:RXN0-5410"],"termid":"GO:0103037"}


id: PBO:0060981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nerve growth factor receptor","termid":"PBO:0060981"}


id: PBO:0068189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 496","termid":"PBO:0068189"}


id: GO:0070256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the regulated release of mucus from a cell or a tissue.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of secretion","termid":"GO:0051048"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of mucus secretion","termid":"GO:0070255"},{"relation_name":"negatively_regulates","term_name":"mucus secretion","termid":"GO:0070254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of mucus secretion","synonyms":[{"name":"negative regulation of mucus production","type":"exact"}],"termid":"GO:0070256"}


id: MONDO:0013471
data:
  {"annotated_genes":["SJAG_01941","SJAG_02463"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86286,86287],"is_not":false,"summary":null,"term":"MONDO:0013471"}]},"cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SLC26A5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01941":null,"SJAG_02463":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 61","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3151230","GARD:22639","MEDGEN:462580","OMIM:613865","DOID:0110513"],"synonyms":[{"name":"DFNB61","type":"narrow"},{"name":"SLC26A5 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 61","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 61","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in SLC26A5","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 61","type":"narrow"},{"name":"deafness, autosomal recessive 61","type":"narrow"},{"name":"deafness, autosomal recessive type 61","type":"narrow"}],"termid":"MONDO:0013471","terms_by_termid":{"MONDO:0013471":null},"xrefs":{"Monarch":{"xref_id":"0013471"}}}


id: PBO:0069817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1103, pseudogene","termid":"PBO:0069817"}


id: FYPO:0001675
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of L-aminoadipate-semialdehyde 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 L-aminoadipate-semialdehyde dehydrogenase activity","termid":"FYPO:0001674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0000661","FYPO:0000654","FYPO:0001985"],"is_obsolete":false,"name":"increased L-aminoadipate-semialdehyde dehydrogenase activity","synonyms":[{"name":"increased alpha-aminoadipate reductase activity","type":"exact"}],"termid":"FYPO:0001675"}


id: GO:0043801
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribulose 5-phosphate + formaldehyde = D-arabino-3-hexulose 6-phosphate.","definition_xrefs":["PMID:16075199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"hexulose-6-phosphate synthase activity","secondary_identifiers":["EC:4.1.2.43","RHEA:25201","MetaCyc:R10-RXN"],"termid":"GO:0043801"}


id: PBO:0082457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-8 sterol isomerase; catalyzes isomerization of delta-8 double bond to delta-7 position at an intermediate step in ergosterol biosynthesis; transcriptionally down-regulated when ergosterol is in excess; mutation is functionally complemented by human EBP","termid":"PBO:0082457"}


id: GO:0007453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures derived from the clypeo-labral disc are generated and organized. This includes the transformation of a clypeo-labal imaginal disc from a monolayered epithelium in the larvae of holometabolous insects into recognizable adult structures including the labrum, anterior and posterior cibarial plates, fish trap bristles, epistomal sclerite and clypeus.","definition_xrefs":["GOC:bf","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc morphogenesis","termid":"GO:0007560"},{"relation_name":"part_of","term_name":"clypeo-labral disc development","termid":"GO:0035213"}],"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":"clypeo-labral disc morphogenesis","synonyms":[{"name":"clypeo-labral disc metamorphosis","type":"exact"},{"name":"morphogenesis of structures derived from the clypeo-labral disc","type":"exact"}],"termid":"GO:0007453"}


id: PBO:0045324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dedicator of cytokinesis 4","termid":"PBO:0045324"}


id: GO:0070159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of coupling threonine to threonyl-tRNA in a mitochondrion, catalyzed by threonyl-tRNA synthetase. In tRNA aminoacylation, the amino acid is first activated by linkage to AMP and then transferred to either the 2'- or the 3'-hydroxyl group of the 3'-adenosine residue of the tRNA.","definition_xrefs":["GOC:mah","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"threonyl-tRNA aminoacylation","termid":"GO:0006435"},{"relation_name":"is_a","term_name":"tRNA aminoacylation for mitochondrial protein translation","termid":"GO:0070127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0140053"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0008150","GO:0006399","GO:0010467","GO:0140053","GO:0006520"],"is_obsolete":false,"name":"mitochondrial threonyl-tRNA aminoacylation","termid":"GO:0070159"}


id: GO:0009683
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving indole-3-acetic acid, a compound which functions as a growth regulator in plants.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxin metabolic process","termid":"GO:0009850"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"indole-containing compound metabolic process","termid":"GO:0042430"}],"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:0008150","GO:0044281"],"is_obsolete":false,"name":"indoleacetic acid metabolic process","synonyms":[{"name":"IAA metabolic process","type":"exact"},{"name":"indole acetic acid metabolic process","type":"exact"},{"name":"indole acetic acid metabolism","type":"exact"},{"name":"indoleacetic acid metabolism","type":"exact"}],"termid":"GO:0009683"}


id: PBO:0058862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 9500","termid":"PBO:0058862"}


id: GO:0097204
data:
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id: PBO:0068033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 338","termid":"PBO:0068033"}


id: GO:0000911
data:
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id: PBO:0031654
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id: GO:0008553
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id: GO:0051337
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id: GO:1904879
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id: GO:0072594
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id: PBO:0079708
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id: SO:1001272
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id: GO:0033706
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id: CHEBI:16240
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id: PBO:0066750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 48","termid":"PBO:0066750"}


id: FYPO:0005062
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the methylation of lysine at position 4 of histone H3 in telomeric regions occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone methylation during vegetative growth","termid":"FYPO:0000869"},{"relation_name":"is_a","term_name":"abnormal histone H3-K4 methylation during vegetative growth","termid":"FYPO:0002330"},{"relation_name":"is_a","term_name":"abnormal histone methylation at telomere during vegetative growth","termid":"FYPO:0007375"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0002274","FYPO:0002494"],"is_obsolete":false,"name":"increased histone H3-K4 methylation at telomere during vegetative growth","synonyms":[{"name":"increased histone H3 K4 methylation at telomere","type":"exact"},{"name":"increased histone H3-K4 methylation at telomere during mitotic cell cycle during vegetative growth","type":"related"},{"name":"increased histone H3-K4 methylation at telomeric region","type":"exact"},{"name":"increased histone H3K4 methylation at telomere","type":"exact"},{"name":"increased histone H3K4me at telomere","type":"exact"},{"name":"increased histone lysine H3 K4 methylation at telomere","type":"exact"}],"termid":"FYPO:0005062"}


id: PBO:0028217
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-septation_following_abnormal_chromosome_segregation,_with_binucleate_and_anucleate_compartment_formation_during_cellular_response_to_salt_stress","termid":"PBO:0028217"}


id: GO:0042303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The periodic casting off and regeneration of an outer covering of cuticle, feathers, hair, horns, skin, etc.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"molting cycle","termid":"GO:0042303"}


id: PBO:0071501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 4","termid":"PBO:0071501"}


id: PBO:0000328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HEAT repeat","termid":"PBO:0000328"}


id: PBO:0044823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 109F (pseudogene)","termid":"PBO:0044823"}


id: MONDO:1010744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atopic dermatitis that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atopic dermatitis, non-human animal","termid":"MONDO:1010126"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atopic dermatitis, domestic cat","secondary_identifiers":["OMIA:000269-9685"],"termid":"MONDO:1010744","xrefs":{"Monarch":{"xref_id":"1010744"}}}


id: FYPO:0005734
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutamate dehydrogenase activity using NAPD+ as a cofactor is decreased during a cellular response to iron ion starvation.","definition_xrefs":["PMID:20435771","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased glutamate dehydrogenase (NADP+) activity","termid":"FYPO:0000983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000654","FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"decreased glutamate dehydrogenase (NADP+) activity during cellular response to iron ion starvation","synonyms":[{"name":"decreased NAD(P)H-dependent glutamate dehydrogenase activity during cellular response to iron ion starvation","type":"exact"},{"name":"decreased NADP-GDH activity during cellular response to iron ion starvation","type":"exact"},{"name":"decreased glutamate dehydrogenase (NADP+) activity during iron ion starvation","type":"exact"}],"termid":"FYPO:0005734"}


id: GO:0048104
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Orientation of hairs or sensory bristles that cover the body surface of an adult, such that they all point in a uniform direction along the plane of the epithelium from which they project.","definition_xrefs":["GOC:jid","GOC:dph","GOC:ascb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of planar polarity","termid":"GO:0001736"}],"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 body hair or bristle planar orientation","termid":"GO:0048104"}


id: GO:0071712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of misfolded proteins transported from the endoplasmic reticulum and targeted to cytoplasmic proteasomes for degradation.","definition_xrefs":["PMID:19520858","PMID:14607247"],"gene_count":0,"genotype_count":0,"name":"obsolete ER-associated misfolded protein catabolic process (obsolete GO:0071712)","synonyms":[{"name":"endoplasmic reticulum-associated misfolded protein catabolism","type":"exact"}],"termid":"GO:0071712"}


id: PBO:0063290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin gamma subfamily B, 4","termid":"PBO:0063290"}


id: MONDO:1011933
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder, non-human animal","termid":"MONDO:0700104"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary surfactant metabolism dysfunction, non-human animal","secondary_identifiers":["OMIA:002251"],"termid":"MONDO:1011933","xrefs":{"Monarch":{"xref_id":"1011933"}}}


id: FYPO:0007976
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A microtubule cytoskeleton organization phenotype observed during anaphase B in which the duration of interpolar microtubule growth events is longer.","definition_xrefs":["PMID:35293864","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal duration of microtubule growth event","termid":"FYPO:0007956"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased duration of interpolar microtubule growth events during anaphase B","termid":"FYPO:0007976"}


id: PBO:0044844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 130C (pseudogene)","termid":"PBO:0044844"}


id: PBO:0082419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bifunctional inositol pyrophosphate kinase and phosphatase; contains an N-terminal PP-InsP kinase domain that phosphorylates inositol hexakisphosphate and heptakisphosphate, and a C-terminal phosphatase domain that hydrolyzes both 1PP-InsP5 and 5PP-InsP5; IP7 levels decrease during starvation, suggesting a role for PP-InsP enzymes in Pi homeostasis; may regulate the dimorphic switch and the function of the cortical actin cytoskeleton","termid":"PBO:0082419"}


id: PBO:0081746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 676","termid":"PBO:0081746"}


id: GO:0075201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly by the symbiont of a threadlike, tubular structure, which may contain multiple nuclei and may or may not be divided internally by septa or cross-walls, for the purpose of penetration into its host organism. In the case of an appressorium existing, this term is defined in further details as the process in which the symbiont penetration peg expands to form a hypha which traverses the epidermal cell and emerges into the intercellular space of the mesophyll tissue. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:26441323","GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formation of infection structure","termid":"GO:0075015"}],"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":"penetration hypha formation","synonyms":[{"name":"formation of symbiont penetration hypha for entry into host","type":"related"},{"name":"symbiont penetration hypha formation for entry into host","type":"related"}],"termid":"GO:0075201"}


id: PBO:0090026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folylpolyglutamate synthase Met7","termid":"PBO:0090026"}


id: PBO:0043174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIR1 pseudogene 1","termid":"PBO:0043174"}


id: MONDO:0003803
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the aortic valve.","direct_ancestors":[{"relation_name":"is_a","term_name":"heart valve disorder","termid":"MONDO:0002869"},{"relation_name":"is_a","term_name":"aortic disorder","termid":"MONDO:0005561"},{"relation_name":"is_a","term_name":"cardiac ventricle disorder","termid":"MONDO:0045001"}],"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":"aortic valve disorder","secondary_identifiers":["ICD9:395","ICD9:424.1","MEDGEN:226776","NCIT:C78650","DOID:62","EFO:0009531","UMLS:C1260873"],"synonyms":[{"name":"aortic valve disease","type":"exact"},{"name":"aortic valve disease or disorder","type":"exact"},{"name":"aortic valve disorder","type":"exact"},{"name":"disease of aortic valve","type":"exact"},{"name":"disease or disorder of aortic valve","type":"exact"},{"name":"disorder of aortic valve","type":"exact"}],"termid":"MONDO:0003803","xrefs":{"Monarch":{"xref_id":"0003803"}}}


id: PR:Q9UT36
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- glo2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UT36"],"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":"hydroxyacylglutathione hydrolase C824.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC824.07","synonyms":[{"name":"Glx II (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-glo2","type":"exact"},{"name":"glyoxalase II (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT36"}


id: PBO:0029850
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_telomeric_heterochromatin_during_vegetative_growth","termid":"PBO:0029850"}


id: MONDO:1011345
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Poisoning that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poisoning, non-human animal","termid":"MONDO:1011345","xrefs":{"Monarch":{"xref_id":"1011345"}}}


id: PBO:0003745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptional activator, MBF subunit Rep2","termid":"PBO:0003745"}


id: GO:0075236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates, maintains or increases the frequency, rate or extent of zoospore movement on or near its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of zoospore movement on or near host (obsolete GO:0075236)","termid":"GO:0075236"}


id: GO:0000315
data:
  {"annotated_genes":["SJAG_01829","SJAG_05218","SJAG_05270","SJAG_00844","SJAG_05221","SJAG_03192","SJAG_03402","SJAG_01478","SJAG_01473","SJAG_02836","SJAG_04889","SJAG_04244","SJAG_06110","SJAG_00799","SJAG_05244","SJAG_04207","SJAG_01727","SJAG_01463","SJAG_01045","SJAG_01591","SJAG_03176","SJAG_03284","SJAG_01719","SJAG_03040","SJAG_04490","SJAG_07009","SJAG_02762","SJAG_04689","SJAG_04493","SJAG_03636","SJAG_02071","SJAG_06253","SJAG_03649","SJAG_00315","SJAG_04216","SJAG_01413","SJAG_04893","SJAG_01303","SJAG_03297","SJAG_00497","SJAG_05573","SJAG_01630","SJAG_00086","SJAG_03459","SJAG_04019"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[98598,90975,100585,114813,105172,103846,111668,88987,113752,101423,111904,112889,97460,102815,114036,114679,115598,114155,116556,96398,107542,105322,114860,116441,115708,110550,87866,112163,117357,107640,95763,98153,110225,102924,88537,103171,112338,95726,97481,102104,107687,104335,109300,96097,106220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005762"}]},"cv_name":"cellular_component","definition":"The larger of the two subunits of an organellar ribosome. Two sites on the ribosomal large subunit are involved in translation: the aminoacyl site (A site) and peptidyl site (P site).","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"large ribosomal subunit","termid":"GO:0015934"},{"relation_name":"part_of","term_name":"organellar ribosome","termid":"GO:0000313"}],"gene_count":45,"genes_by_uniquename":{"SJAG_00086":null,"SJAG_00315":null,"SJAG_00497":null,"SJAG_00799":null,"SJAG_00844":null,"SJAG_01045":null,"SJAG_01303":null,"SJAG_01413":null,"SJAG_01463":null,"SJAG_01473":null,"SJAG_01478":null,"SJAG_01591":null,"SJAG_01630":null,"SJAG_01719":null,"SJAG_01727":null,"SJAG_01829":null,"SJAG_02071":null,"SJAG_02762":null,"SJAG_02836":null,"SJAG_03040":null,"SJAG_03176":null,"SJAG_03192":null,"SJAG_03284":null,"SJAG_03297":null,"SJAG_03402":null,"SJAG_03459":null,"SJAG_03636":null,"SJAG_03649":null,"SJAG_04019":null,"SJAG_04207":null,"SJAG_04216":null,"SJAG_04244":null,"SJAG_04490":null,"SJAG_04493":null,"SJAG_04689":null,"SJAG_04889":null,"SJAG_04893":null,"SJAG_05218":null,"SJAG_05221":null,"SJAG_05244":null,"SJAG_05270":null,"SJAG_05573":null,"SJAG_06110":null,"SJAG_06253":null,"SJAG_07009":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:0032991","GO:0005575"],"is_obsolete":false,"name":"organellar large ribosomal subunit","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000315","terms_by_termid":{"GO:0005762":null}}


id: GO:1901205
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of a cardiac adrenergic receptor signaling pathway.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11","GOC:TermGenie","GOC:rl"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of adrenergic receptor signaling pathway involved in heart process (obsolete GO:1901205)","synonyms":[{"name":"down regulation of adrenergic receptor signaling pathway involved in heart process","type":"exact"},{"name":"down regulation of adrenergic receptor signalling pathway involved in heart process","type":"exact"},{"name":"down regulation of beta-adrenergic receptor signalling pathway involved in heart process","type":"narrow"},{"name":"down-regulation of adrenergic receptor signaling pathway involved in heart process","type":"exact"},{"name":"down-regulation of adrenergic receptor signalling pathway involved in heart process","type":"exact"},{"name":"down-regulation of beta-adrenergic receptor signalling pathway involved in heart process","type":"narrow"},{"name":"downregulation of adrenergic receptor signaling pathway involved in heart process","type":"exact"},{"name":"downregulation of adrenergic receptor signalling pathway involved in heart process","type":"exact"},{"name":"downregulation of beta-adrenergic receptor signalling pathway involved in heart process","type":"narrow"},{"name":"inhibition of adrenergic receptor signaling pathway involved in heart process","type":"narrow"},{"name":"inhibition of adrenergic receptor signalling pathway involved in heart process","type":"exact"},{"name":"inhibition of beta-adrenergic receptor signalling pathway involved in heart process","type":"narrow"},{"name":"negative regulation of adrenergic receptor signalling pathway involved in heart process","type":"exact"},{"name":"negative regulation of beta-adrenergic receptor signalling pathway involved in heart process","type":"narrow"}],"termid":"GO:1901205"}


id: PBO:0063938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIMREG pseudogene 3","termid":"PBO:0063938"}


id: GO:0002428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigen-presenting cell expresses peptide antigen in association with an MHC class Ib protein complex on its cell surface. The peptide antigen may originate from an endogenous or exogenous protein. Class Ib here refers to non-classical class I molecules, such as those of the HLA-E family.","definition_xrefs":["GOC:add","PMID:15928678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation via MHC class Ib","termid":"GO:0002475"},{"relation_name":"is_a","term_name":"antigen processing and presentation of peptide antigen","termid":"GO:0048002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"antigen processing and presentation of peptide antigen via MHC class Ib","synonyms":[{"name":"peptide antigen processing and presentation via MHC class Ib","type":"exact"}],"termid":"GO:0002428"}


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


id: PBO:0085211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Oxysterol-binding phosphatidylserine transferase; part of family with seven members in S. cerevisiae; family members have overlapping, redundant functions in sterol metabolism and collectively perform a function essential for viability; OSH7 has a paralog, OSH6, that arose from the whole genome duplication","termid":"PBO:0085211"}


id: GO:0086015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An action potential that occurs in a sinoatrial node cardiac muscle cell.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell action potential","termid":"GO:0086001"},{"relation_name":"part_of","term_name":"SA node cell to atrial cardiac muscle cell signaling","termid":"GO:0086018"}],"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":"SA node cell action potential","synonyms":[{"name":"SA node cardiac muscle cell action potential","type":"exact"},{"name":"SAN cardiac muscle cell action potential","type":"exact"},{"name":"sinoatrial node cardiac muscle cell action potential","type":"exact"},{"name":"sinus node cardiac muscle cell action potential","type":"narrow"}],"termid":"GO:0086015"}


id: GO:0036110
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 deprivation of inositol.","definition_xrefs":["GOC:al","PMID:19606215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to starvation","termid":"GO:0009267"}],"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 inositol starvation","termid":"GO:0036110"}


id: GO:0051351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ligase activity, the catalysis of the ligation of two substances with concomitant breaking of a diphosphate linkage, usually in a nucleoside triphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catalytic activity","termid":"GO:0043085"}],"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 ligase activity","synonyms":[{"name":"activation of ligase activity","type":"narrow"},{"name":"ligase activator","type":"exact"},{"name":"stimulation of ligase activity","type":"narrow"},{"name":"up regulation of ligase activity","type":"exact"},{"name":"up-regulation of ligase activity","type":"exact"},{"name":"upregulation of ligase activity","type":"exact"}],"termid":"GO:0051351"}


id: PR:Q10092
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hsp3104 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10092"],"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":"glutathione-independent glyoxalase hsp3104 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11D3.13","synonyms":[{"name":"Spom972h-hsp3104","type":"exact"},{"name":"glyoxalase 3 homolog 4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"heat shock protein 31 homolog 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10092"}


id: PBO:0073500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small glutamine rich tetratricopeptide repeat co-chaperone alpha","termid":"PBO:0073500"}


id: GO:0003405
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental growth that results in the lengthening of the optic vesicle in the posterior direction.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental growth involved in morphogenesis","termid":"GO:0060560"},{"relation_name":"part_of","term_name":"optic vesicle morphogenesis","termid":"GO:0003404"}],"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":"optic vesicle elongation","termid":"GO:0003405"}


id: PBO:0060050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 38","termid":"PBO:0060050"}


id: PBO:0055364
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 2793","termid":"PBO:0055364"}


id: PBO:0042547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 11B","termid":"PBO:0042547"}


id: GO:0060063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of the specialized region of the embryonic shield of the embryo that acts as the main signaling center establishing the teleost body plan.","definition_xrefs":["GOC:dph","PMID:9442883"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Spemann organizer formation","termid":"GO:0060061"}],"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":"Spemann organizer formation at the embryonic shield","synonyms":[{"name":"Spemann's organizer formation at the embryonic shield","type":"exact"},{"name":"Spemann-Mangold organizer formation at the embryonic shield","type":"exact"}],"termid":"GO:0060063"}


id: GO:0015549
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of carbonyl cyanide m-chlorophenylhydrazone from one side of a membrane to the other. Carbonyl cyanide m-chlorophenylhydrazone is a proton ionophore, commonly used as an uncoupling agent and inhibitor of photosynthesis because of its effects on mitochondrial and chloroplast membranes.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete carbonyl cyanide m-chlorophenylhydrazone transmembrane transporter activity (obsolete GO:0015549)","synonyms":[{"name":"CCCP transporter activity","type":"exact"},{"name":"carbonyl cyanide m-chlorophenylhydrazone transporter activity","type":"related"},{"name":"carbonyl cyanide m-chlorophenylhydrazone/nalidixic acid/organomercurials:hydrogen antiporter activity","type":"related"}],"termid":"GO:0015549"}


id: PBO:0063078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pappalysin 1","termid":"PBO:0063078"}


id: PBO:0084706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane ADP/ATP translocator; exchanges cytosolic ADP for mitochondrially synthesized ATP; expressed under anaerobic conditions; similar to Aac1p; has roles in maintenance of viability and in respiration; AAC3 has a paralog, PET9, that arose from the whole genome duplication","termid":"PBO:0084706"}


id: PBO:0062882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian adenocarcinoma amplified long non-coding RNA","termid":"PBO:0062882"}


id: PBO:0002312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal-ubiquitin fusion protein Ubi1 (predicted)","termid":"PBO:0002312"}


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


id: FYPO:0004340
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which mitochondrial fission, the division of a mitochondrion into two or more separate compartments, is abnormal.","definition_xrefs":["GO:0000266","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrion organization","termid":"FYPO:0000809"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal mitochondrial fission","synonyms":[{"name":"abnormal mitochondrial division","type":"exact"},{"name":"abnormal mitochondrial fission during mitotic cell cycle","type":"related"},{"name":"abnormal mitochondrial fission during vegetative growth","type":"exact"},{"name":"abnormal mitochondrial proliferation","type":"related"}],"termid":"FYPO:0004340"}


id: MONDO:0016877
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 12","termid":"MONDO:0017277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of the long arm of chromosome 12","secondary_identifiers":["icd11.foundation:1206066048","MEDGEN:1826014","Orphanet:261821","GARD:20800","UMLS:C5679656"],"synonyms":[{"name":"partial deletion of chromosome 12q","type":"exact"},{"name":"partial deletion of the long arm of chromosome type 12","type":"exact"},{"name":"partial monosomy of chromosome 12q","type":"exact"},{"name":"partial monosomy of the long arm of chromosome 12","type":"exact"}],"termid":"MONDO:0016877","xrefs":{"Monarch":{"xref_id":"0016877"}}}


id: GO:1903404
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of renal phosphate excretion.","definition_xrefs":["GOC:pm","GOC:TermGenie","GO_REF:0000058","PMID:8700837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of renal phosphate excretion","termid":"GO:1903402"},{"relation_name":"positively_regulates","term_name":"renal phosphate excretion","termid":"GO:0044722"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of renal phosphate excretion","synonyms":[{"name":"activation of renal phosphate excretion","type":"narrow"},{"name":"activation of renal phosphate ion excretion","type":"narrow"},{"name":"positive regulation of renal phosphate ion excretion","type":"exact"},{"name":"up regulation of renal phosphate excretion","type":"exact"},{"name":"up regulation of renal phosphate ion excretion","type":"exact"},{"name":"up-regulation of renal phosphate excretion","type":"exact"},{"name":"up-regulation of renal phosphate ion excretion","type":"exact"},{"name":"upregulation of renal phosphate excretion","type":"exact"},{"name":"upregulation of renal phosphate ion excretion","type":"exact"}],"termid":"GO:1903404"}


id: MONDO:0009328
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":"hemangiomatosis, cutaneous, with associated features","secondary_identifiers":["OMIM:234800","UMLS:C0220738","MESH:C562438","MEDGEN:67397"],"synonyms":[{"name":"hemangiomatosis, cutaneous, with associated features","type":"exact"}],"termid":"MONDO:0009328","xrefs":{"Monarch":{"xref_id":"0009328"}}}


id: FYPO:0001146
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 misfolded glycoprotein degradation is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased proteasomal ubiquitin-dependent protein degradation","termid":"FYPO:0004545"}],"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:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002274","FYPO:0001985","FYPO:0002494","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased misfolded glycoprotein degradation during vegetative growth","synonyms":[{"name":"decreased misfolded glycoprotein catabolic process during vegetative growth","type":"exact"},{"name":"decreased misfolded glycoprotein catabolism during vegetative growth","type":"exact"},{"name":"decreased misfolded glycoprotein degradation during mitotic cell cycle","type":"related"},{"name":"reduced misfolded glycoprotein degradation during vegetative growth","type":"exact"}],"termid":"FYPO:0001146"}


id: MONDO:0004065
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Choroid melanoma characterized by the presence of intermediate cells which are similar to but smaller than epithelioid cells.","definition_xrefs":["NCIT:C6100"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant choroid melanoma","termid":"MONDO:0003878"},{"relation_name":"is_a","term_name":"intermediate cell type uveal melanoma","termid":"MONDO:0004062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004992"],"is_obsolete":false,"name":"intermediate cell type choroid melanoma","secondary_identifiers":["DOID:6996","MEDGEN:272760","UMLS:C1334208"],"synonyms":[{"name":"Intermediate cell type choroid melanoma","type":"exact"},{"name":"intermediate cell type uveal melanoma of optic choroid","type":"exact"},{"name":"mixed cell melanoma of choroid","type":"exact"},{"name":"optic choroid intermediate cell type uveal melanoma","type":"exact"}],"termid":"MONDO:0004065","xrefs":{"Monarch":{"xref_id":"0004065"}}}


id: FYPO:0006144
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 gluconate measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased cellular gluconate level","synonyms":[{"name":"decreased cellular gluconate level during mitotic cell cycle","type":"related"},{"name":"decreased cellular gluconate level during vegetative growth","type":"exact"},{"name":"decreased gluconate accumulation","type":"related"},{"name":"reduced cellular gluconate level","type":"exact"}],"termid":"FYPO:0006144"}


id: PBO:0026882
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_chromatin_at_RNA_polymerase_II-regulated_genes_during_nitrogen_starvation","termid":"PBO:0026882"}


id: PBO:0029824
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_curved_vegetative_cell_population_(obsolete_FYPO:0002413)","termid":"PBO:0029824"}


id: PBO:0029902
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_chromatin_silencing","termid":"PBO:0029902"}


id: PBO:0050804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HtrA serine peptidase 4","termid":"PBO:0050804"}


id: PBO:0074837
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 31B","termid":"PBO:0074837"}


id: SO:0001872
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a chromosome, where the chromosome has undergone a large structural rearrangement that altered the genome organization. There is no longer synteny to the reference genome.","definition_xrefs":["NCBI:th","PMID:18564416"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"},{"relation_name":"is_a","term_name":"structural_alteration","termid":"SO:0001785"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rearrangement_region","synonyms":[{"name":"rearrangement region","type":"exact"}],"termid":"SO:0001872"}


id: GO:0034013
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an aliphatic aldoxime = an aliphatic nitrile + H2O.","definition_xrefs":["RHEA:11316"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrogen-oxygen hydrolyase activity","termid":"GO:0141122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"aliphatic aldoxime dehydratase activity","secondary_identifiers":["EC:4.8.1.2","MetaCyc:4.99.1.5-RXN"],"synonyms":[{"name":"aliphatic aldoxime hydro-lyase activity","type":"exact"}],"termid":"GO:0034013"}


id: PBO:0017530
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Multicopy suppressor of Sporulation Abnormal mutant","termid":"PBO:0017530"}


id: PBO:0061645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUDT19 pseudogene 3","termid":"PBO:0061645"}


id: GO:0052452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism modulates the frequency, rate or extent of the innate immune response of the symbiont organism; the innate immune response is the symbiont's first line of defense against infection. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of symbiont innate immunity (obsolete GO:0052452)","synonyms":[{"name":"modulation by organism of symbiont innate immunity","type":"exact"},{"name":"modulation of symbiont innate immune response","type":"exact"}],"termid":"GO:0052452"}


id: MONDO:1010170
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Krabbe 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":"leukodystrophy, non-human animal","termid":"MONDO:1010238"},{"relation_name":"is_a","term_name":"peripheral neuropathy, non-human animal","termid":"MONDO:1010239"},{"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":"Krabbe disease, non-human animal","secondary_identifiers":["OMIA:000578"],"termid":"MONDO:1010170","xrefs":{"Monarch":{"xref_id":"1010170"}}}


id: PBO:0041565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 20 open reading frame 85","termid":"PBO:0041565"}


id: GO:0140527
data:
  {"annotated_genes":["SJAG_02295","SJAG_00266","SJAG_01677","SJAG_07002","SJAG_02616","SJAG_00980","SJAG_01156","SJAG_03720","SJAG_00100","SJAG_01419","SJAG_05295","SJAG_04303","SJAG_00908","SJAG_02465","SJAG_02822","SJAG_00377","SJAG_00935","SJAG_03525","SJAG_04950","SJAG_04748","SJAG_02267","SJAG_05373","SJAG_03221","SJAG_01076","SJAG_00727","SJAG_02460","SJAG_04205","SJAG_03219","SJAG_02708","SJAG_02181","SJAG_02294","SJAG_02652","SJAG_03751","SJAG_03567","SJAG_01410","SJAG_00623","SJAG_02311","SJAG_02339","SJAG_00172","SJAG_00757","SJAG_03438","SJAG_05333","SJAG_01044","SJAG_01138","SJAG_02592","SJAG_02556","SJAG_02490","SJAG_01708","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107433],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0010846"},{"annotations":[107126,116241,98559,88057,88674],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990918"},{"annotations":[110576,89849,109109,108206,104346],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010780"},{"annotations":[109758,107128],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010772"},{"annotations":[109759,96421,92384,101012,87997,107129,100038,116546],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000709"},{"annotations":[100039,87998,92385],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010774"},{"annotations":[107436],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0045128"},{"annotations":[101867,107817],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905263"},{"annotations":[88575],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0010845"},{"annotations":[107439,100074,107132,89801,88064,90318,104347,106192,114981,103813,104319,89850,92256,103352,88576,101014,94253,118200,100139,90983,110577,89109,92751,100635,88807,116550,100041,96422,92184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007131"},{"annotations":[93884,115731,88681],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010520"},{"annotations":[76405,116890,118201,105663,109782,101016,107612,108544,116739,116552],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000712"},{"annotations":[115680],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0062209"}]},"cv_name":"biological_process","definition":"A DNA recombination process that results in the bidirectional exchange of genetic material between highly homologous DNA molecules.","definition_xrefs":["PMID:17846636"],"direct_ancestors":[{"relation_name":"is_a","term_name":"homologous recombination","termid":"GO:0035825"}],"gene_count":49,"genes_by_uniquename":{"SJAG_00100":null,"SJAG_00172":null,"SJAG_00266":null,"SJAG_00377":null,"SJAG_00623":null,"SJAG_00727":null,"SJAG_00757":null,"SJAG_00908":null,"SJAG_00935":null,"SJAG_00980":null,"SJAG_01044":null,"SJAG_01076":null,"SJAG_01138":null,"SJAG_01156":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01677":null,"SJAG_01708":null,"SJAG_02181":null,"SJAG_02267":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02311":null,"SJAG_02339":null,"SJAG_02460":null,"SJAG_02465":null,"SJAG_02490":null,"SJAG_02556":null,"SJAG_02592":null,"SJAG_02616":null,"SJAG_02652":null,"SJAG_02708":null,"SJAG_02822":null,"SJAG_03048":null,"SJAG_03219":null,"SJAG_03221":null,"SJAG_03438":null,"SJAG_03525":null,"SJAG_03567":null,"SJAG_03720":null,"SJAG_03751":null,"SJAG_04205":null,"SJAG_04303":null,"SJAG_04748":null,"SJAG_04950":null,"SJAG_05295":null,"SJAG_05333":null,"SJAG_05373":null,"SJAG_07002":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006310","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"reciprocal homologous recombination","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0140527","terms_by_termid":{"GO:0000709":null,"GO:0000712":null,"GO:0007131":null,"GO:0010520":null,"GO:0010772":null,"GO:0010774":null,"GO:0010780":null,"GO:0010845":null,"GO:0010846":null,"GO:0045128":null,"GO:0062209":null,"GO:1905263":null,"GO:1990918":null}}


id: MONDO:0018068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterized by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation.","definition_xrefs":["Orphanet:3378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"excluded_subClassOf","term_name":"obsolete chromosomal anomaly with cataract (obsolete MONDO:0020226)","termid":"MONDO:0020226"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital vitreoretinal dysplasia","termid":"MONDO:0020247"},{"relation_name":"is_a","term_name":"chromosome 13 disorder","termid":"MONDO:0700020"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0002320"],"is_obsolete":false,"name":"trisomy 13","secondary_identifiers":["icd11.foundation:1435958084","SCTID:21111006","UMLS:C0152095","NANDO:2200964","MESH:C536305","ICD9:758.1","NCIT:C101223","NCIT:C36529","MedDRA:10044686","NORD:1796","GARD:7341","DOID:11665","MEDGEN:56261"],"synonyms":[{"name":"D trisomy syndrome (formerly)","type":"related"},{"name":"D1 trisomy","type":"related"},{"name":"Patau syndrome","type":"exact"},{"name":"Patau's syndrome","type":"exact"},{"name":"Trisomy 13 Syndrome","type":"exact"},{"name":"chromosome 13, trisomy 13 complete","type":"related"},{"name":"trisomy 13","type":"exact"},{"name":"trisomy type 13","type":"exact"}],"termid":"MONDO:0018068","xrefs":{"Monarch":{"xref_id":"0018068"}}}


id: PBO:0075383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRY-box transcription factor 30","termid":"PBO:0075383"}


id: PBO:0040894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bone morphogenetic protein receptor type 1B","termid":"PBO:0040894"}


id: GO:1900230
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of single-species biofilm formation in or on host organism.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of single-species biofilm formation","termid":"GO:1900192"},{"relation_name":"is_a","term_name":"regulation of single-species biofilm formation in or on host organism","termid":"GO:1900228"},{"relation_name":"positively_regulates","term_name":"single-species biofilm formation in or on host organism","termid":"GO:0044407"}],"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 single-species biofilm formation in or on host organism","synonyms":[{"name":"activation of single-species biofilm formation in or on host organism","type":"narrow"},{"name":"up regulation of single-species biofilm formation in or on host organism","type":"exact"},{"name":"up-regulation of single-species biofilm formation in or on host organism","type":"exact"},{"name":"upregulation of single-species biofilm formation in or on host organism","type":"exact"}],"termid":"GO:1900230"}


id: MONDO:0007734
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare disorder caused by mutations in the TGIF gene mapped to chromosome 18p11.3. It is characterized by semilobar holoprosencephaly, hypotelorism, and ptosis.","definition_xrefs":["NCIT:C75475"],"direct_ancestors":[{"relation_name":"is_a","term_name":"holoprosencephaly","termid":"MONDO:0016296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"holoprosencephaly 4","secondary_identifiers":["MEDGEN:374488","OMIM:142946","UMLS:C1840528","DOID:0110880","MESH:C564180"],"synonyms":[{"name":"HPE4","type":"exact"},{"name":"TGIF1 holoprosencephaly","type":"exact"},{"name":"holoprosencephaly 4","type":"exact"},{"name":"holoprosencephaly caused by mutation in TGIF1","type":"exact"},{"name":"holoprosencephaly type 4","type":"exact"}],"termid":"MONDO:0007734","xrefs":{"Monarch":{"xref_id":"0007734"}}}


id: PBO:0049980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIKESHI pseudogene 1","termid":"PBO:0049980"}


id: GO:0007442
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the hindgut are generated and organized.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"digestive tract morphogenesis","termid":"GO:0048546"},{"relation_name":"part_of","term_name":"hindgut development","termid":"GO:0061525"}],"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":"hindgut morphogenesis","termid":"GO:0007442"}


id: RO:0002633
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of ectoparasite of","direct_ancestors":[{"relation_name":"is_a","term_name":"parasitized_by","termid":"RO:0002445"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_ectoparasite","termid":"RO:0002633"}


id: GO:0043982
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H4 by the addition of an acetyl group to a lysine residue at position 8 of the histone.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H4-K8 acetylation (obsolete GO:0043982)","synonyms":[{"name":"histone H4 acetylation at K8","type":"exact"}],"termid":"GO:0043982"}


id: PBO:0074786
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 7","termid":"PBO:0074786"}


id: MONDO:0011650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any atrioventricular septal defect in which the cause of the disease is a mutation in the CRELD1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrioventricular septal defect, susceptibility to, 2","secondary_identifiers":["MEDGEN:381193","UMLS:C1853508","MESH:C565249","OMIM:606217"],"synonyms":[{"name":"AVSD2","type":"related"},{"name":"CRELD1 atrioventricular septal defect","type":"exact"},{"name":"atrioventricular septal defect caused by mutation in CRELD1","type":"exact"},{"name":"atrioventricular septal defect, partial, with heterotaxy syndrome","type":"related"},{"name":"atrioventricular septal defect, susceptibility to, 2","type":"exact"},{"name":"atrioventricular septal defect, susceptibility to, type 2","type":"exact"},{"name":"susceptibility to atrioventricular septal defect 2","type":"related"}],"termid":"MONDO:0011650","xrefs":{"Monarch":{"xref_id":"0011650"}}}


id: PBO:0058607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6739","termid":"PBO:0058607"}


id: PBO:0066353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reticulocalbin 1 pseudogene 1","termid":"PBO:0066353"}


id: PBO:0058329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4703","termid":"PBO:0058329"}


id: PBO:0060448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEDD8 activating enzyme E1 subunit 1","termid":"PBO:0060448"}


id: PBO:0004145
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed during nucleotide depletion","termid":"PBO:0004145"}


id: PBO:0040072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin domain containing 1","termid":"PBO:0040072"}


id: PBO:0045173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member A2","termid":"PBO:0045173"}


id: PBO:0085092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear exosome exonuclease component; has 3'-5' exonuclease activity that is regulated by Lrp1p; involved in RNA processing, maturation, surveillance, degradation, tethering, and export; role in sn/snoRNAs precursor degradation; forms a stable heterodimer with Lrp1p; has similarity to E. coli RNase D and to human PM-Sc1 100 (EXOSC10); mutant displays reduced transcription elongation in the G-less-based","termid":"PBO:0085092"}


id: MONDO:0043131
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46,XX disorder of sex development","termid":"MONDO:0017576"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Michels Caskey syndrome","secondary_identifiers":["GARD:3590","MEDGEN:419102","MESH:C537576","UMLS:C2931537"],"synonyms":[{"name":"Mullerian aplasia with hypoplastic thumbs","type":"related"},{"name":"Mullerian aplasia with unilateral hypoplasia of the thumbs and skeletal spine deformities","type":"related"}],"termid":"MONDO:0043131","xrefs":{"Monarch":{"xref_id":"0043131"}}}


id: PBO:0046799
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coagulation factor V","termid":"PBO:0046799"}


id: PR:G2TRR4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- new19 gene.","definition_xrefs":["UniProtKB:G2TRR4","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":"microsomal signal peptidase subunit 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC887.22","synonyms":[{"name":"Spom972h-new19","type":"exact"}],"termid":"PR:G2TRR4"}


id: MONDO:0012622
data:
  {"annotated_genes":["SJAG_04094"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86445],"is_not":false,"summary":null,"term":"MONDO:0012622"}]},"cv_name":"mondo","definition":"This disease is characterized by progressive cerebellar ataxia with pyramidal and spinal cord dysfunction, associated with distinctive MRI anomalies and increased lactate in the abnormal white matter.","definition_xrefs":["Orphanet:137898"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04094":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NORD:1941","MESH:C567009","MEDGEN:370845","OMIM:611105","UMLS:C1970180","GARD:12652","SCTID:703537008"],"synonyms":[{"name":"LBSL","type":"exact"},{"name":"Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation","type":"exact"},{"name":"leukoencephalopathy with brain stem and spinal cord involvement - high lactate","type":"related"},{"name":"leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation","type":"related"},{"name":"leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation","type":"related"},{"name":"leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome","type":"exact"},{"name":"leukoencephalopathy with brain stem and spinal cord involvement-lactate elevation syndrome","type":"exact"},{"name":"leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation","type":"related"},{"name":"mitochondrial aspartyl-tRNA synthetase deficiency","type":"related"}],"termid":"MONDO:0012622","terms_by_termid":{"MONDO:0012622":null},"xrefs":{"Monarch":{"xref_id":"0012622"}}}


id: PBO:0030857
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_calcium_level_during_cellular_response_to_salt_stress","termid":"PBO:0030857"}


id: MONDO:0003793
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete uterine carcinosarcoma (obsolete MONDO:0003793)","termid":"MONDO:0003793","xrefs":{"Monarch":{"xref_id":"0003793"}}}


id: GO:1902274
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of (R)-carnitine transmembrane transport.","definition_xrefs":["GOC:TermGenie","PMID:23755272"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of transmembrane transport","termid":"GO:0034764"},{"relation_name":"is_a","term_name":"regulation of (R)-carnitine transmembrane transport","termid":"GO:1902272"},{"relation_name":"positively_regulates","term_name":"(R)-carnitine transmembrane transport","termid":"GO:1902270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"positive regulation of (R)-carnitine transmembrane transport","synonyms":[{"name":"activation of (R)-carnitine transmembrane transport","type":"narrow"},{"name":"up regulation of (R)-carnitine transmembrane transport","type":"exact"},{"name":"up-regulation of (R)-carnitine transmembrane transport","type":"exact"},{"name":"upregulation of (R)-carnitine transmembrane transport","type":"exact"}],"termid":"GO:1902274"}


id: GO:1905389
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 leukotriene B4 stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:14656734"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to fatty acid","termid":"GO:0070542"}],"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 leukotriene B4","synonyms":[{"name":"response to LTB4","type":"exact"}],"termid":"GO:1905389"}


id: PBO:0090010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L22","termid":"PBO:0090010"}


id: MONDO:0021441
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the exocrine pancreas.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic exocrine neoplasm","termid":"MONDO:0021076"},{"relation_name":"is_a","term_name":"benign neoplasm of pancreas","termid":"MONDO:0021470"}],"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":"benign neoplasm of exocrine pancreas","secondary_identifiers":["MEDGEN:138080","NCIT:C4613","SCTID:271956003","UMLS:C0347285","DOID:0080781"],"synonyms":[{"name":"benign exocrine pancreas neoplasm","type":"exact"},{"name":"benign exocrine pancreas tumor","type":"exact"},{"name":"benign exocrine pancreas tumour","type":"exact"},{"name":"benign exocrine pancreatic neoplasm","type":"exact"},{"name":"benign neoplasm of the exocrine pancreas","type":"exact"},{"name":"benign tumor of exocrine pancreas","type":"exact"},{"name":"benign tumor of the exocrine pancreas","type":"exact"},{"name":"benign tumour of exocrine pancreas","type":"exact"},{"name":"benign tumour of the exocrine pancreas","type":"exact"},{"name":"exocrine pancreas benign neoplasm","type":"exact"}],"termid":"MONDO:0021441","xrefs":{"Monarch":{"xref_id":"0021441"}}}


id: GO:0045353
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Blocks the binding of interleukin-1 to interleukin-1 type II receptors.","definition_xrefs":["GOC:ebc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interleukin-1 receptor antagonist activity","termid":"GO:0005152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0140678","GO:0003674","GO:0005515","GO:0005488","GO:0098772"],"is_obsolete":false,"name":"interleukin-1 type II receptor antagonist activity","synonyms":[{"name":"IL-1ra type II","type":"exact"}],"termid":"GO:0045353"}


id: MONDO:0004267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign squamous neoplasm characterized by a papillary growth pattern, diffusely involving a specific anatomic site.","definition_xrefs":["NCIT:C9009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillomatosis","termid":"MONDO:0021098"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"squamous papillomatosis","secondary_identifiers":["MEDGEN:235130","DOID:7532","UMLS:C1378340","ICDO:8060/0"],"synonyms":[{"name":"squamous papillomatosis","type":"exact"}],"termid":"MONDO:0004267","xrefs":{"Monarch":{"xref_id":"0004267"}}}


id: MONDO:0015353
data:
  {"annotated_genes":["SJAG_01352"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84849],"is_not":false,"summary":null,"term":"MONDO:0015353"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neuronopathy, distal hereditary motor, type 5","termid":"MONDO:0100350"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01352":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0000426","MONDO:0005244"],"is_obsolete":false,"name":"neuronopathy, distal hereditary motor, type 5A","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18266","DOID:0111204","OMIM:600794"],"synonyms":[{"name":"HMN 5A","type":"exact"},{"name":"HMN5A","type":"exact"},{"name":"dHMN 5A","type":"exact"},{"name":"dHMN5","type":"broad"},{"name":"distal HMN V","type":"broad"},{"name":"distal hereditary motor neuropathy type V","type":"broad"},{"name":"distal spinal muscular atrophy type 5","type":"broad"},{"name":"neuronopathy, distal hereditary motor, type 5","type":"broad"},{"name":"neuronopathy, distal hereditary motor, type 5A","type":"exact"},{"name":"neuronopathy, distal hereditary motor, type VA","type":"exact"},{"name":"neuropathy, distal hereditary motor, type 5A","type":"exact"},{"name":"spinal muscular atrophy, distal, type 5","type":"broad"},{"name":"spinal muscular atrophy, distal, type 5A","type":"exact"},{"name":"spinal muscular atrophy, distal, with upper limb predominance","type":"exact"}],"termid":"MONDO:0015353","terms_by_termid":{"MONDO:0015353":null},"xrefs":{"Monarch":{"xref_id":"0015353"}}}


id: MONDO:0014263
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 8","termid":"MONDO:0016907"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"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":"8q24.3 microdeletion syndrome","secondary_identifiers":["OMIM:615583","MEDGEN:816353","GARD:12814","UMLS:C3810023","Orphanet:508488"],"synonyms":[{"name":"VRJS","type":"related"},{"name":"Verheij syndrome","type":"exact"},{"name":"chromosome 8Q24.3 deletion syndrome","type":"related"}],"termid":"MONDO:0014263","xrefs":{"Monarch":{"xref_id":"0014263"}}}


id: PBO:0059442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane spanning 4-domains A13","termid":"PBO:0059442"}


id: MONDO:0019646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital megacalycosis","termid":"MONDO:0019639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"unilateral congenital megacalycosis","secondary_identifiers":["MEDGEN:1842948","GARD:19179","UMLS:C5681456","Orphanet:93176"],"termid":"MONDO:0019646","xrefs":{"Monarch":{"xref_id":"0019646"}}}


id: MONDO:0020382
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multifocal pattern dystrophy simulating fundus flavimaculatus is a patterned dystrophy of the retinal pigment epithelium characterized by multiple yellowish irregular flecks scattered or interconnected around the macula, simulating what is observed in Stargardt disease, and usually asymptomatic until adulthood when patients present with a slowly progressive loss of vision that often only becomes apparent in old age.","definition_xrefs":["Orphanet:99003"],"direct_ancestors":[{"relation_name":"is_a","term_name":"patterned dystrophy of the retinal pigment epithelium","termid":"MONDO:0018973"}],"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":"multifocal pattern dystrophy simulating fundus flavimaculatus","secondary_identifiers":["ICD10CM:H35.5","GARD:19612","MEDGEN:1376850","icd11.foundation:1819044742","SCTID:723408004","UMLS:C4509881"],"synonyms":[{"name":"multifocal pattern dystrophy simulating Stargardt disease","type":"exact"}],"termid":"MONDO:0020382","xrefs":{"Monarch":{"xref_id":"0020382"}}}


id: PBO:0091915
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRE1-Like","termid":"PBO:0091915"}


id: PBO:0063944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl cis/trans isomerase, NIMA-interacting 4 pseudogene 1","termid":"PBO:0063944"}


id: PBO:0061453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor subfamily 5 group A member 1","termid":"PBO:0061453"}


id: GO:1901379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of potassium ion transmembrane transport.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of potassium ion transport","termid":"GO:0043266"},{"relation_name":"is_a","term_name":"regulation of monoatomic cation transmembrane transport","termid":"GO:1904062"},{"relation_name":"regulates","term_name":"potassium ion transmembrane transport","termid":"GO:0071805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"regulation of potassium ion transmembrane transport","synonyms":[{"name":"regulation of potassium ion membrane transport","type":"exact"}],"termid":"GO:1901379"}


id: GO:0050570
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-(phosphooxy)-L-threonine + NAD+ = 3-amino-2-oxopropyl phosphate + CO2 + NADH.","definition_xrefs":["EC:1.1.1.262","RHEA:32275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"4-hydroxythreonine-4-phosphate dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN-13179"],"synonyms":[{"name":"L-threonine 4-phosphate dehydrogenase activity","type":"related"},{"name":"NAD(+)-dependent threonine 4-phosphate dehydrogenase activity","type":"related"},{"name":"NAD+-dependent threonine 4-phosphate dehydrogenase activity","type":"related"}],"termid":"GO:0050570"}


id: FYPO:0007701
data:
  {"alleles_by_uniquename":{"SJAG_04332:allele-1":{"allele_type":"amino_acid_mutation","description":"I30T,T572P","gene_uniquename":"SJAG_04332","name":"cdc25-D9","uniquename":"SJAG_04332:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118973],"is_not":false,"summary":null,"term":"FYPO:0007701"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, is longer than normal, has one nucleus, and the mitotic cell cycle is arrested with nuclei at the mitotic G2/M phase transition.","definition_xrefs":["PMID:33683349","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated mononucleate vegetative cell","termid":"FYPO:0004255"},{"relation_name":"is_a","term_name":"inviable elongated cell with cell cycle arrest at mitotic G2/M phase transition","termid":"FYPO:0007702"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04332":null},"genotype_count":1,"genotypes_by_uniquename":{"cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cdc25-D9(I30T,T572P aa)","display_uniquename":"cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04332:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0000004","FYPO:0001320","FYPO:0005447","FYPO:0000005","FYPO:0001985"],"is_obsolete":false,"name":"inviable elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition","references_by_uniquename":{"PMID:25866389":null},"single_locus_annotated_genes":["SJAG_04332"],"single_locus_genotype_uniquenames":["cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"inviable elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition during mitotic cell cycle","type":"related"},{"name":"inviable elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition during vegetative growth","type":"exact"},{"name":"inviable elongated mononucleate cell with cell cycle arrest in mitotic G2 phase","type":"related"},{"name":"inviable elongated mononucleate vegetative cell with cell cycle arrest at mitotic G2/M phase transition","type":"exact"},{"name":"lethal; elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition","type":"exact"}],"termid":"FYPO:0007701","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000137":null,"FYPO:0007701":null,"FYPO_EXT:0000001":null}}


id: MONDO:0007587
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"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":"external auditory canal atresia-vertical talus-hypertelorism syndrome","secondary_identifiers":["MEDGEN:361813","UMLS:C1876181","GARD:4638","OMIM:133705","Orphanet:3023"],"synonyms":[{"name":"Rasmussen Johnsen Thomsen syndrome","type":"related"},{"name":"Rasmussen syndrome","type":"related"},{"name":"Rasmussen-Johnsen-Thomsen syndrome","type":"exact"},{"name":"external auditory canal, bilateral atresia of, with congenital vertical talus","type":"related"},{"name":"inherited congenital bilateral atresia of the external auditory canal, congenital bilateral vertical talus and increased interocular distance","type":"related"}],"termid":"MONDO:0007587","xrefs":{"Monarch":{"xref_id":"0007587"}}}


id: PBO:0067428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 547, pseudogene","termid":"PBO:0067428"}


id: GO:0071232
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 histidine stimulus.","definition_xrefs":["GOC:mah"],"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 organic cyclic compound","termid":"GO:0071407"},{"relation_name":"is_a","term_name":"response to histidine","termid":"GO:0080052"},{"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"}],"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 histidine","termid":"GO:0071232"}


id: PBO:0027716
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_nucleosome_occupancy","termid":"PBO:0027716"}


id: MONDO:0030259
data:
  {"annotated_genes":["SJAG_00639"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86037],"is_not":false,"summary":null,"term":"MONDO:0030259"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pontocerebellar hypoplasia","termid":"MONDO:0020135"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00639":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"pontocerebellar hypoplasia, type 15","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619302","UMLS:C5543326","GARD:18563","DOID:0112326","MEDGEN:1781311"],"synonyms":[{"name":"PCH15","type":"exact"},{"name":"pontocerebellar hypoplasia, type 15","type":"exact"}],"termid":"MONDO:0030259","terms_by_termid":{"MONDO:0030259":null},"xrefs":{"Monarch":{"xref_id":"0030259"}}}


id: PR:000027566
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H2A-alpha phosphorylated 2 in Schizosaccharomyces pombe. Example: UniProtKB:P04909-1, Ser-122, MOD:00046.","definition_xrefs":["PMID:19965387","PomBase:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2A-alpha (Schizosaccharomyces pombe 972h-)","termid":"PR:P04909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hta1/Phos(S121)","pombase_gene_id":"SPCC622.08c","synonyms":[{"name":"PomBase_original_PRO_term_name: histone H2A-alpha phosphorylated 2 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hta1/Phos:2","type":"exact"},{"name":"histone H2A.1 phosphorylated 2 (Schizosaccharomyces pombe)","type":"exact"},{"name":"hta1/Phos(S121)","type":"exact"},{"name":"hta1/Phos:(S122)","type":"exact"}],"termid":"PR:000027566"}


id: PBO:0072872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SATB homeobox 2","termid":"PBO:0072872"}


id: MONDO:0010457
data:
  {"annotated_genes":["SJAG_04631"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86417],"is_not":false,"summary":null,"term":"MONDO:0010457"}]},"cv_name":"mondo","definition":"Ogden syndrome is a rare, genetic progeroid syndrome characterized by a variable phenotype including postnatal growth delay, severe global developmental delay, hypotonia, non-specific dysmorphic facies with aged appearance and cryptorchidism, as well as cardiac arrthymias and skeletal anomalies. Patients typically present with widely opened fontanels, mainly truncal hypotonia, a waddling gait with hypertonia of the extremities, small hands and feet, broad great toes, scoliosis and redundant skin with lack of subcutaneous fat.","definition_xrefs":["Orphanet:276432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progeroid syndrome","termid":"MONDO:0015333"},{"relation_name":"is_a","term_name":"NAA10-related syndrome","termid":"MONDO:0100124"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04631":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0019303"],"is_obsolete":false,"name":"Ogden syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:300855","DOID:0050781","HGNC:7645","NCIT:C188215","UMLS:C3275447","MESH:C536107","MEDGEN:477078","GARD:17281"],"synonyms":[{"name":"Acetyl-CoA:arylamine n-acetyltransferase","type":"related"},{"name":"N acetyltransferase 1 deficiency","type":"related"},{"name":"N acetyltransferase deficiency","type":"related"},{"name":"N-alpha-acetyltransferase","type":"exact"},{"name":"N-terminal acetyltransferase deficiency","type":"exact"},{"name":"NAT1 deficiency","type":"related"},{"name":"OGDNS","type":"exact"},{"name":"Ogden syndrome","type":"exact"},{"name":"Ogden syndrome, X-linked recessive, X-linked dominant","type":"exact"},{"name":"X-linked malformation and infantile lethality syndrome","type":"exact"},{"name":"arylamine n-acetyltransferase 1","type":"related"},{"name":"premature ageing appearance-developmental delay-cardiac arrhythmia syndrome","type":"exact"},{"name":"premature aging appearance-developmental delay-cardiac arrhythmia syndrome","type":"exact"}],"termid":"MONDO:0010457","terms_by_termid":{"MONDO:0010457":null},"xrefs":{"Monarch":{"xref_id":"0010457"}}}


id: GO:0031176
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the endohydrolysis of (1->4)-beta-D-xylosidic linkages in xylans.","definition_xrefs":["EC:3.2.1.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xylanase activity","termid":"GO:0097599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016798","GO:0003824"],"is_obsolete":false,"name":"endo-1,4-beta-xylanase activity","secondary_identifiers":["MetaCyc:3.2.1.8-RXN"],"synonyms":[{"name":"1,4-beta-D-xylan xylanohydrolase activity","type":"related"},{"name":"1,4-beta-xylan xylanohydrolase activity","type":"related"},{"name":"beta-1,4-xylan xylanohydrolase activity","type":"related"},{"name":"beta-1,4-xylanase activity","type":"related"},{"name":"beta-D-xylanase activity","type":"related"},{"name":"beta-xylanase activity","type":"related"},{"name":"endo-(1,4)-beta-xylanase(1,4)-beta-xylan 4-xylanohydrolase activity","type":"related"},{"name":"endo-(1->4)-beta-xylanase(1->4)-beta-xylan 4-xylanohydrolase activity","type":"related"},{"name":"endo-1,4-beta-D-xylanase activity","type":"related"},{"name":"endo-1,4-xylanase activity","type":"related"},{"name":"endo-beta-1,4-xylanase activity","type":"related"},{"name":"xylanase","type":"broad"}],"termid":"GO:0031176"}


id: PBO:0078238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 20-1","termid":"PBO:0078238"}


id: GO:0099605
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that regulates the frequency of action potentials in a spike train.","definition_xrefs":["ISBN:978-0071390118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of action potential","termid":"GO:0098900"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of action potential firing rate","termid":"GO:0099605"}


id: MONDO:0005484
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis.","definition_xrefs":["NCIT:C5673"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colorectal neoplasm","termid":"MONDO:0005335"},{"relation_name":"is_a","term_name":"digestive system adenoma","termid":"MONDO:0006180"}],"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":"colorectal adenoma","secondary_identifiers":["SCTID:399432003","DOID:0050860","DOID:0050914","UMLS:C1302401","EFO:0005406","MEDGEN:224904"],"synonyms":[{"name":"adenoma of large bowel","type":"exact"},{"name":"adenoma of large intestine","type":"exact"},{"name":"adenoma of the large bowel","type":"exact"},{"name":"adenoma of the large intestine","type":"exact"},{"name":"colorectal adenoma","type":"exact"},{"name":"colorectum adenoma","type":"exact"},{"name":"large bowel adenoma","type":"exact"},{"name":"large intestine adenoma","type":"exact"}],"termid":"MONDO:0005484","xrefs":{"Monarch":{"xref_id":"0005484"}}}


id: MONDO:0013365
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 9p23-p21.2.","definition_xrefs":["DOID:0110528"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 83","secondary_identifiers":["UMLS:C3888310","GARD:22637","OMIM:613685","MEDGEN:854856"],"synonyms":[{"name":"DFNB83","type":"narrow"},{"name":"autosomal recessive deafness 83","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 83","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 83","type":"narrow"},{"name":"deafness, autosomal recessive 83","type":"narrow"}],"termid":"MONDO:0013365","xrefs":{"Monarch":{"xref_id":"0013365"}}}


id: GO:0008949
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + oxalyl-CoA = CO2 + formyl-CoA.","definition_xrefs":["EC:4.1.1.8","RHEA:19333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"oxalyl-CoA decarboxylase activity","secondary_identifiers":["MetaCyc:OXALYL-COA-DECARBOXYLASE-RXN","KEGG_REACTION:R01908"],"synonyms":[{"name":"oxalyl coenzyme A decarboxylase activity","type":"related"},{"name":"oxalyl-CoA carboxy-lyase (formyl-CoA-forming)","type":"related"},{"name":"oxalyl-CoA carboxy-lyase activity","type":"related"}],"termid":"GO:0008949"}


id: PR:O74450
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pop23 gene.","definition_xrefs":["UniProtKB:O74450","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":"ribonucleases P/MRP protein subunit pop3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16C4.05","synonyms":[{"name":"RNA-processing protein pop3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-pop23","type":"exact"}],"termid":"PR:O74450"}


id: FYPO:0006608
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which a protein that is normally localized intermittently to the Cdr2 medial cortical node complex shows a pattern of localization to the complex over time that is not correlated with cell size as normal.","definition_xrefs":["PMID:29514920","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal intermittent protein localization to Cdr2 medial cortical node complex","termid":"FYPO:0006607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"intermittent protein localization to Cdr2 medial cortical node complex decoupled from cell size","synonyms":[{"name":"bursts of intermittent protein localization to Cdr2 medial cortical node complex decoupled from cell size","type":"related"},{"name":"intermittent protein localization to Cdr2 medial cortical node complex decoupled from cell size during mitotic cell cycle","type":"related"},{"name":"intermittent protein localization to Cdr2 medial cortical node complex decoupled from cell size during vegetative growth","type":"exact"},{"name":"loss of correlation between intermittent protein localization to Cdr2 medial cortical node complex and cell size","type":"exact"},{"name":"pattern of protein visits to Cdr2 medial cortical node complex decoupled from cell size","type":"related"},{"name":"protein localization bursts to Cdr2 medial cortical node complex decoupled from cell size","type":"related"},{"name":"transient protein localization to Cdr2 medial cortical node complex decoupled from cell size","type":"exact"}],"termid":"FYPO:0006608"}


id: GO:0004443
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: D-myo-inositol 3,4-bisphosphate + H2O = D-myo-inositol 3-monophosphate + phosphate.","definition_xrefs":["EC:3.1.3.66","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete inositol-1,4,-bisphosphate 4-phosphatase (obsolete GO:0004443)","synonyms":[{"name":"inositol-1,4,-bisphosphate 4-phosphatase","type":"exact"}],"termid":"GO:0004443"}


id: GO:0008548
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: GTP + H2O = GDP + phosphate. Activity is associated with the signal-recognition particle, a protein and RNA-containing structure involved in endoplasmic reticulum-associated protein synthesis.","definition_xrefs":["EC:3.6.5.4","MetaCyc:3.6.1.49-RXN"],"gene_count":0,"genotype_count":0,"name":"obsolete signal-recognition-particle GTPase activity (obsolete GO:0008548)","synonyms":[{"name":"signal-recognition-particle GTPase activity","type":"exact"}],"termid":"GO:0008548"}


id: GO:0004674
data:
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SA-450463","Reactome:R-HSA-9022314","Reactome:R-HSA-163418","Reactome:R-HSA-202222","Reactome:R-HSA-9610153","Reactome:R-HSA-163416","Reactome:R-HSA-112342","Reactome:R-HSA-170055","Reactome:R-HSA-3239019","Reactome:R-HSA-198611","Reactome:R-HSA-3371435","Reactome:R-HSA-5632672","Reactome:R-HSA-8940100","Reactome:R-HSA-377186","Reactome:R-HSA-3371567","Reactome:R-HSA-3858480","Reactome:R-HSA-442724","Reactome:R-HSA-8948146","Reactome:R-HSA-5635841","Reactome:R-HSA-3928640","Reactome:R-HSA-9815501","Reactome:R-HSA-188350","Reactome:R-HSA-166286","Reactome:R-HSA-77071","Reactome:R-HSA-195283","Reactome:R-HSA-165777","Reactome:R-HSA-5690250","Reactome:R-HSA-9613530","Reactome:R-HSA-9835011","Reactome:R-HSA-2028661","Reactome:R-HSA-6798374","Reactome:R-HSA-199935","Reactome:R-HSA-6795460","Reactome:R-HSA-934559","Reactome:R-HSA-198731","Reactome:R-HSA-3209160","Reactome:R-HSA-9652165","Reactome:R-HSA-1638803","Reactome:R-HSA-176298","Reactome:R-HSA-9860800","Reactome:R-HSA-4793911","Reactome:R-HSA-6805479","Reactome:R-HSA-9007539","Reactome:R-HSA-4608825","Reactome:R-HSA-8873929","Reactome:R-HSA-198347","Reactome:R-HSA-109862","Reactome:R-HSA-2399992","Reactome:R-HSA-9008480","Reactome:R-HSA-211583","Reactome:R-HSA-428961","Reactome:R-HSA-1181156","Reactome:R-HSA-2399966","Reactome:R-HSA-5671763","Reactome:R-HSA-5683425","Reactome:R-HSA-5668947","Reactome:R-HSA-2574840","Reactome:R-HSA-419087","Reactome:R-HSA-198746","Reactome:R-HSA-2028555","Reactome:R-HSA-446701","Reactome:R-HSA-450337","Reactome:R-HSA-5687094","Reactome:R-HSA-9824994","Reactome:R-HSA-5682026","Reactome:R-HSA-2028679","Reactome:R-HSA-1632857","Reactome:R-HSA-187688","Reactome:R-HSA-198609","Reactome:R-HSA-419083","Reactome:R-HSA-3229102","Reactome:R-HSA-9619515","Reactome:R-HSA-9648888","Reactome:R-HSA-445072","Reactome:R-HSA-3222006","Reactome:R-HSA-2243942","Reactome:R-HSA-448948","Reactome:R-HSA-8852317","Reactome:R-HSA-8944454","Reactome:R-HSA-165726","Reactome:R-HSA-5693598","Reactome:R-HSA-9769115","Reactome:R-HSA-9831712","Reactome:R-HSA-6802926","Reactome:R-HSA-6810233","Reactome:R-HSA-9762094","Reactome:R-HSA-166119","Reactome:R-HSA-2730876","Reactome:R-HSA-3928620","Reactome:R-HSA-429714","Reactome:R-HSA-1362270","Reactome:R-HSA-198613","Reactome:R-HSA-8854908","Reactome:R-HSA-5675198","Reactome:R-HSA-975853","Reactome:R-HSA-200421","Reactome:R-HSA-6811454","Reactome:R-HSA-4332388","Reactome:R-HSA-5607722","Reactome:R-HSA-6805059","Reactome:R-HSA-9818789","Reactome:R-HSA-399950","Reactome:R-HSA-450222","Reactome:R-HSA-9032863","Reactome:R-HSA-448955","Reactome:R-HSA-8853419","Reactome:R-HSA-9729300","Reactome:R-HSA-2399941","Reactome:R-HSA-3229152","Reactome:R-HSA-9604328","Reactome:R-HSA-912470","Reactome:R-HSA-5672978","Reactome:R-HSA-399978","Reactome:R-HSA-6805785","Reactome:R-HSA-2466068","Reactome:R-HSA-198621","Reactome:R-HSA-75028","Reactome:R-HSA-9817397","Reactome:R-HSA-195275","Reactome:R-HSA-1449597","Reactome:R-HSA-201717","Reactome:R-HSA-9731111","Reactome:R-HSA-2028598","Reactome:R-HSA-8932322","Reactome:R-HSA-9612980","Reactome:R-HSA-5671919","Reactome:R-HSA-399939","Reactome:R-HSA-2028629","Reactome:R-HSA-5260201","Reactome:R-HSA-5672010","Reactome:R-HSA-4411402","Reactome:R-HSA-5218826","Reactome:R-HSA-211164","Reactome:R-HSA-193647","Reactome:R-HSA-199299","Reactome:R-HSA-5687121","Reactome:R-HSA-9824582","Reactome:R-HSA-166284","Reactome:R-HSA-198599","Reactome:R-HSA-5672828","Reactome:R-HSA-2399985","Reactome:R-HSA-9032751","Reactome:R-HSA-8868344","Reactome:R-HSA-167084","Reactome:R-HSA-5229343","Reactome:R-HSA-5082405","Reactome:R-HSA-211650","Reactome:R-HSA-109702","Reactome:R-HSA-1181149","Reactome:R-HSA-6805640","Reactome:R-HSA-9796081","Reactome:R-HSA-69604","Reactome:R-HSA-163010","Reactome:R-HSA-168053","Reactome:R-HSA-8939963","Reactome:R-HSA-6788392","Reactome:R-HSA-442739","Reactome:R-HSA-199917","Reactome:R-HSA-399944","Reactome:R-HSA-9766532","Reactome:R-HSA-3000327","Reactome:R-HSA-446694","Reactome:R-HSA-9831514","Reactome:R-HSA-5357472","Reactome:R-HSA-9705323","Reactome:R-HSA-2029460","Reactome:R-HSA-5607742","Reactome:R-HSA-3132737","Reactome:R-HSA-6801675","Reactome:R-HSA-3928577","Reactome:R-HSA-392752","Reactome:R-HSA-450474","Reactome:R-HSA-5357477","Reactome:R-HSA-419197","Reactome:R-HSA-5687090","Reactome:R-HSA-6802911","Reactome:R-HSA-6795290","Reactome:R-HSA-198270","Reactome:R-HSA-201691","Reactome:R-HSA-2470508","Reactome:R-HSA-5684140","Reactome:R-HSA-9725030","Reactome:R-HSA-2399996","Reactome:R-HSA-8853444","Reactome:R-HSA-9824999","Reactome:R-HSA-399951","Reactome:R-HSA-1168638","Reactome:R-HSA-200143","Reactome:R-HSA-166245","Reactome:R-HSA-202500","Reactome:R-HSA-5686704","Reactome:R-HSA-198371","Reactome:R-HSA-6799332","Reactome:R-HSA-9853369","Reactome:R-HSA-349444","Reactome:R-HSA-5693540","Reactome:R-HSA-165758","Reactome:R-HSA-1454699","Reactome:R-HSA-2399982","Reactome:R-HSA-9824897","Reactome:R-HSA-111970","Reactome:R-HSA-195318","Reactome:R-HSA-8878054","Reactome:R-HSA-5672973","GO:0004695","Reactome:R-HSA-1458463","Reactome:R-HSA-9610156","Reactome:R-HSA-5693609","Reactome:R-HSA-450499","Reactome:R-HSA-5682598","Reactome:R-HSA-5693575","Reactome:R-HSA-6802933","Reactome:R-HSA-9861642","Reactome:R-HSA-2028583","Reactome:R-HSA-349455","Reactome:R-HSA-6804276","Reactome:R-HSA-9834076","Reactome:R-HSA-168184","Reactome:R-HSA-199298","Reactome:R-HSA-2399981","Reactome:R-HSA-349426","Reactome:R-HSA-9825704","Reactome:R-HSA-937059","Reactome:R-HSA-8877691","Reactome:R-HSA-2399969","GO:0004696","Reactome:R-HSA-3228469","Reactome:R-HSA-3239014","Reactome:R-HSA-5672948","Reactome:R-HSA-975134","Reactome:R-HSA-2422927","Reactome:R-HSA-2028284","Reactome:R-HSA-9612501","Reactome:R-HSA-2028635","Reactome:R-HSA-6804955","Reactome:R-HSA-2730856","Reactome:R-HSA-5693549","Reactome:R-HSA-975160","Reactome:R-HSA-5218854","Reactome:R-HSA-198756","Reactome:R-HSA-9758486","Reactome:R-HSA-3857329","Reactome:R-HSA-6805285","Reactome:R-HSA-381111","Reactome:R-HSA-2730896","Reactome:R-HSA-6795473","Reactome:R-HSA-6799246","Reactome:R-HSA-9705320","Reactome:R-HSA-69685","Reactome:R-HSA-4332358","Reactome:R-HSA-170087","Reactome:R-HSA-202459","Reactome:R-HSA-8852306","Reactome:R-HSA-9839363","Reactome:R-HSA-156699","Reactome:R-HSA-1445144","Reactome:R-HSA-8863895","Reactome:R-HSA-9773803","Reactome:R-HSA-5683801","Reactome:R-HSA-9855910","Reactome:R-HSA-5218821","Reactome:R-HSA-918229","GO:0106311","Reactome:R-HSA-6805103","Reactome:R-HSA-9610163","Reactome:R-HSA-9627089","Reactome:R-HSA-165718","Reactome:R-HSA-5082387","Reactome:R-HSA-5218916","Reactome:R-HSA-5683964","Reactome:R-HSA-419644","Reactome:R-HSA-139908","Reactome:R-HSA-975180","Reactome:R-HSA-2529020","Reactome:R-HSA-389756","Reactome:R-HSA-975861","Reactome:R-HSA-202510","Reactome:R-HSA-9819106","Reactome:R-HSA-2399977","Reactome:R-HSA-8868567","Reactome:R-HSA-2028589","Reactome:R-HSA-9632868","Reactome:R-HSA-9832782","Reactome:R-HSA-156673","Reactome:R-HSA-2214351","Reactome:R-HSA-450827","Reactome:R-HSA-8942836","Reactome:R-HSA-199895","Reactome:R-HSA-9824977","Reactome:R-HSA-8933446","Reactome:R-HSA-9009208","Reactome:R-HSA-187949","Reactome:R-HSA-5357831","Reactome:R-HSA-3772435","Reactome:R-HSA-5686578","Reactome:R-HSA-5684887","Reactome:R-HSA-2430535","Reactome:R-HSA-6802935","Reactome:R-HSA-156678","Reactome:R-HSA-1225894","Reactome:R-HSA-8952289","Reactome:R-HSA-69891","Reactome:R-HSA-5687086","Reactome:R-HSA-975878","Reactome:R-HSA-8856813","Reactome:R-HSA-3857328","Reactome:R-HSA-5632670","Reactome:R-HSA-6802919","Reactome:R-HSA-8863011","Reactome:R-HSA-4551570","Reactome:R-HSA-165766","Reactome:R-HSA-450346","Reactome:R-HSA-380272"],"synonyms":[{"name":"protein serine kinase activity","type":"narrow"},{"name":"protein serine-threonine kinase activity","type":"related"},{"name":"protein threonine kinase activity","type":"narrow"},{"name":"protein-serine kinase activity","type":"narrow"},{"name":"serine kinase activity","type":"narrow"},{"name":"serine protein kinase activity","type":"narrow"},{"name":"serine(threonine) protein kinase activity","type":"related"},{"name":"serine-specific protein kinase activity","type":"narrow"},{"name":"serine/threonine protein kinase activity","type":"related"},{"name":"threonine-specific protein kinase activity","type":"narrow"}],"termid":"GO:0004674","terms_by_termid":{"GO:0004674":null,"GO:0004676":null,"GO:0004683":null,"GO:0004691":null,"GO:0004693":null,"GO:0004694":null,"GO:0004697":null,"GO:0004699":null,"GO:0004706":null,"GO:0004707":null,"GO:0004709":null,"GO:0004711":null,"GO:0004740":null,"GO:0008349":null,"GO:0008353":null,"GO:0035175":null,"GO:0072354":null,"GO:0072371":null,"GO:0140834":null,"GO:0140836":null}}


id: MONDO:0020282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete metabolic disease with macular cherry-red spot (obsolete MONDO:0020282)","secondary_identifiers":["Orphanet:98714"],"termid":"MONDO:0020282","xrefs":{"Monarch":{"xref_id":"0020282"}}}


id: MONDO:0017027
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary interstitial lung disease specific to adulthood (obsolete MONDO:0017027)","secondary_identifiers":["Orphanet:264740"],"synonyms":[{"name":"primary ILD specific to adulthood","type":"exact"}],"termid":"MONDO:0017027","xrefs":{"Monarch":{"xref_id":"0017027"}}}


id: GO:0019975
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a member of the interleukin-17 family of cytokines.","definition_xrefs":["GOC:jl","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine binding","termid":"GO:0019955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"interleukin-17 binding","synonyms":[{"name":"IL-17 binding","type":"exact"}],"termid":"GO:0019975"}


id: MONDO:0026404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X inactivation, familial skewed","termid":"MONDO:0100209"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X inactivation, familial skewed, 1","secondary_identifiers":["UMLS:C1848138","MESH:C564716","MEDGEN:338394","OMIM:300087"],"synonyms":[{"name":"SXI1","type":"related"},{"name":"X INACTIVATION, FAMILIAL SKEWED, 1","type":"related"},{"name":"X inactivation, familial skewed, 1","type":"exact"},{"name":"X-inactivation, familial skewed","type":"exact"},{"name":"X-inactivation, familial skewed, 1","type":"exact"}],"termid":"MONDO:0026404","xrefs":{"Monarch":{"xref_id":"0026404"}}}


id: GO:0018962
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 3-phenylpropionate, the anion of phenylpropanoic acid. It is produced from putrefaction of proteins in soil or breakdown of several constituents of plants, such as lignin, various oils and resins.","definition_xrefs":["GOC:ai","UM-BBD_pathwayID:ppa"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"3-phenylpropionate metabolic process","synonyms":[{"name":"3-phenylpropionate metabolism","type":"exact"},{"name":"hydrocinnamic acid metabolic process","type":"exact"},{"name":"hydrocinnamic acid metabolism","type":"exact"},{"name":"phenylpropanoate metabolic process","type":"exact"},{"name":"phenylpropanoate metabolism","type":"exact"}],"termid":"GO:0018962"}


id: GO:0060201
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a clathrin-sculpted acetylcholine transport vesicle.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport vesicle membrane","termid":"GO:0030658"},{"relation_name":"is_a","term_name":"clathrin-coated vesicle membrane","termid":"GO:0030665"},{"relation_name":"part_of","term_name":"clathrin-sculpted acetylcholine transport vesicle","termid":"GO:0060200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005737","GO:0031410","GO:0005575"],"is_obsolete":false,"name":"clathrin-sculpted acetylcholine transport vesicle membrane","synonyms":[{"name":"clathrin sculpted acetylcholine constitutive secretory pathway transport vesicle membrane","type":"exact"},{"name":"clathrin sculpted acetylcholine transport vesicle membrane","type":"exact"}],"termid":"GO:0060201"}


id: PBO:0042539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 7","termid":"PBO:0042539"}


id: PBO:0051640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IMP U3 small nucleolar ribonucleoprotein 4","termid":"PBO:0051640"}


id: MONDO:0971105
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"neonatal renal venous thrombosis","secondary_identifiers":["Orphanet:664912"],"termid":"MONDO:0971105","xrefs":{"Monarch":{"xref_id":"0971105"}}}


id: MONDO:0005016
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis.","definition_xrefs":["NCIT:C84417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"},{"relation_name":"is_a","term_name":"chronic kidney disease","termid":"MONDO:0005300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005240"],"is_obsolete":false,"name":"diabetic kidney disease","secondary_identifiers":["icd11.foundation:615062102","EFO:0000401","SCTID:127013003","SCTID:50620007","ICD9:583.81","UMLS:C0011881","ICD9:250.4","MEDGEN:8352","MESH:D003928","ICD9:250.40"],"synonyms":[{"name":"DKD","type":"exact"},{"name":"diabetic nephropathy","type":"exact"},{"name":"type 1 diabetes nephropathy","type":"narrow"},{"name":"type 2 diabetes nephropathy","type":"narrow"}],"termid":"MONDO:0005016","xrefs":{"Monarch":{"xref_id":"0005016"}}}


id: FYPO:0001055
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An inviable phenotype in which a cell enters mitosis normally, in that the spindle forms normally and chromosomes condense normally, but then undergoes septation despite abnormal chromosome segregation, giving rise to a cut phenotype.","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cut","termid":"FYPO:0000229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000032"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"has_part","termid":"FYPO:0000337"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000641"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000337","FYPO:0000032","FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000004","FYPO:0000641"],"is_obsolete":false,"name":"cut following normal mitotic chromosome condensation","synonyms":[{"name":"cut following normal chromosome condensation during mitotic cell cycle","type":"exact"},{"name":"cut following normal entry into mitosis","type":"related"},{"name":"cut following normal mitotic chromosome condensation during vegetative growth","type":"exact"},{"name":"cut following normal mitotic entry","type":"related"},{"name":"cut with normal mitotic chromosome condensation","type":"exact"},{"name":"septation following abnormal mitotic chromosome segregation, with normal chromosome condensation","type":"exact"}],"termid":"FYPO:0001055"}


