# terms

id: PBO:0040001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor like GTPase 13B","termid":"PBO:0040001"}


id: PBO:0040879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bone morphogenetic protein 4","termid":"PBO:0040879"}


id: GO:0044674
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A hexameric complex consisting of three polypeptides in an alpha2beta2gamma2 arrangement. Involved in the reduction of the coenzyme M-bound methyl group to methane, which is the final step in methanogenesis.","definition_xrefs":["GOC:mengo_curators","PMID:9367957"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"methyl coenzyme M reductase complex","termid":"GO:0044674"}


id: PBO:0072202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S18 pseudogene 1","termid":"PBO:0072202"}


id: GO:0140210
data:
  {"annotated_genes":["SJAG_02336","SJAG_02761","SJAG_01297","SJAG_03540"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102309,105836,110231,120698],"is_not":false,"summary":null,"term":"GO:0140210"}]},"cv_name":"biological_process","definition":"Any process in which a protein is transported to the kinetochore along a microtubule.","definition_xrefs":["PMID:25472718"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to kinetochore","termid":"GO:0034501"},{"relation_name":"is_a","term_name":"establishment of protein localization to chromosome","termid":"GO:0070199"},{"relation_name":"is_a","term_name":"protein transport along microtubule","termid":"GO:0098840"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01297":null,"SJAG_02336":null,"SJAG_02761":null,"SJAG_03540":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"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"protein transport along microtubule to kinetochore","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140210","terms_by_termid":{"GO:0140210":null}}


id: FYPO:0000262
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which cells do not respond normally to reactive oxygen species, resulting in accumulation of oxidative damage including DNA damage, during G0 phase.","definition_xrefs":["PomBase:mah","PMID:19197239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to oxidative stress","termid":"FYPO:0000180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal cellular response to reactive oxygen species during G0","synonyms":[{"name":"abnormal cellular response to reactive oxygen species during cell quiescence","type":"exact"},{"name":"abnormal cellular response to reactive oxygen species during quiescence","type":"exact"},{"name":"protects against physiological oxidative damage in G0","type":"related"}],"termid":"FYPO:0000262"}


id: PBO:0025497
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic Trna thioUridilase","termid":"PBO:0025497"}


id: PBO:0044684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDIT4L antisense RNA 1","termid":"PBO:0044684"}


id: FYPO:0004015
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which a cell contains a normal number of mitochondria.","definition_xrefs":["PMID:2065367","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitochondrion","termid":"FYPO:0006034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"mitochondria present in normal numbers","synonyms":[{"name":"mitochondria present in normal numbers during mitotic cell cycle","type":"exact"},{"name":"mitochondria present in normal numbers during vegetative growth","type":"exact"}],"termid":"FYPO:0004015"}


id: PBO:0013076
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does not functionally complement E. coli hisA","termid":"PBO:0013076"}


id: MONDO:0013406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any age-related macular degeneration in which the cause of the disease is a mutation in the RAX2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"age-related macular degeneration","termid":"MONDO:0005150"}],"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":"age related macular degeneration 6","secondary_identifiers":["MEDGEN:462410","MESH:C563674","OMIM:613757","DOID:0110018","UMLS:C3151060"],"synonyms":[{"name":"ARMD6","type":"exact"},{"name":"RAX2 age-related macular degeneration","type":"exact"},{"name":"age related macular degeneration type 6","type":"exact"},{"name":"age-related macular degeneration caused by mutation in RAX2","type":"exact"},{"name":"macular Degeneration, age-related, type 6","type":"exact"},{"name":"macular degeneration, age-related, 6","type":"related"}],"termid":"MONDO:0013406","xrefs":{"Monarch":{"xref_id":"0013406"}}}


id: GO:0014906
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a myotube cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell. This occurs as part of the process of skeletal muscle regeneration. Myotubes are multinucleated cells that are formed when proliferating myoblasts exit the cell cycle, differentiate and fuse.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myotube cell development","termid":"GO:0014904"},{"relation_name":"part_of","term_name":"myotube differentiation involved in skeletal muscle regeneration","termid":"GO:0014908"}],"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":"myotube cell development involved in skeletal muscle regeneration","termid":"GO:0014906"}


id: PBO:0066308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBPJ pseudogene 2","termid":"PBO:0066308"}


id: MONDO:0009239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FSHB gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadotropic hypogonadism","termid":"MONDO:0018555"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 24 without anosmia","secondary_identifiers":["MESH:C537070","MEDGEN:1806136","Orphanet:52901","UMLS:C5574957","GARD:10128","DOID:0090088","OMIM:229070","SCTID:758664007"],"synonyms":[{"name":"FSHB hypogonadotropic hypogonadism","type":"exact"},{"name":"HH24","type":"related"},{"name":"follicle-stimulating hormone deficiency, isolated","type":"related"},{"name":"hypogonadotropic hypogonadism 24 without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism caused by mutation in FSHB","type":"exact"},{"name":"isolated FSH deficiency","type":"exact"},{"name":"isolated follicle stimulating hormone deficiency","type":"related"},{"name":"isolated follicle-stimulating hormone (FSH) deficiency","type":"related"},{"name":"isolated follicle-stimulating hormone deficiency","type":"exact"}],"termid":"MONDO:0009239","xrefs":{"Monarch":{"xref_id":"0009239"}}}


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


id: PBO:0027454
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_triphosphatase_activity","termid":"PBO:0027454"}


id: GO:2000437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of monocyte extravasation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular extravasation","termid":"GO:0002691"},{"relation_name":"is_a","term_name":"regulation of mononuclear cell migration","termid":"GO:0071675"},{"relation_name":"regulates","term_name":"monocyte extravasation","termid":"GO:0035696"}],"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 monocyte extravasation","termid":"GO:2000437"}


id: PBO:0005295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-amylase homolog Aah3","termid":"PBO:0005295"}


id: PBO:0079884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uroplakin 3B like 1","termid":"PBO:0079884"}


id: MONDO:0019509
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cutaneous leukocytoclastic angiitis is a small-vessel vasculitis presenting with palpable purpura and urticarial lesions which predate the purpuric lesions most frequently observed on the legs. Systemic symptoms including fever, cough, hemoptysis, sinusitis, arthralgia, arthritis, myalgia, abdominal pain, diarrhea, hematochezia, paresthesia, weakness, and hematuria may be observed. Skin biopsy reveals exudates rich in neutrophils, endothelial damage, fibrin deposition, and leukocytoclasis in postcapillary venules of small vessels. Cutaneous leukocytoclastic angiitis can be idiopathic (in up to 50% of cases) or secondary to infections, medications (such as antituberculosis medication), collagen vascular diseases, or neoplasms.","definition_xrefs":["Orphanet:889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune complex mediated vasculitis","termid":"MONDO:0015491"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cutaneous leukocytoclastic angiitis","secondary_identifiers":["icd11.foundation:71458216","UMLS:C4049638","MEDGEN:881641","NCIT:C122919","GARD:7851","SCTID:718217000"],"synonyms":[{"name":"cutaneous hypersensitivity vasculitis","type":"exact"},{"name":"cutaneous leukocytoclastic vasculitis","type":"exact"},{"name":"cutaneous small vessel vasculitis","type":"exact"},{"name":"cutaneous small-vessel vasculitis","type":"exact"},{"name":"hypersensitivity angiitis","type":"exact"},{"name":"leukocytoclastic angiitis","type":"related"}],"termid":"MONDO:0019509","xrefs":{"Monarch":{"xref_id":"0019509"}}}


id: MONDO:0020592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder that affects the pharynx. Representative examples include pharyngitis and carcinoma.","definition_xrefs":["NCIT:C26850"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disorder of pharynx","secondary_identifiers":["UMLS:C0031345","SCTID:75860007","MEDGEN:10691"],"synonyms":[{"name":"chordate pharynx disease","type":"exact"},{"name":"chordate pharynx disease or disorder","type":"exact"},{"name":"disease of chordate pharynx","type":"exact"},{"name":"disease or disorder of chordate pharynx","type":"exact"},{"name":"disorder of chordate pharynx","type":"exact"},{"name":"pharyngeal disease","type":"exact"},{"name":"pharyngeal disorder","type":"exact"}],"termid":"MONDO:0020592","xrefs":{"Monarch":{"xref_id":"0020592"}}}


id: PBO:0090902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NuA4 histone acetyltransferase complex subunit Eaf7","termid":"PBO:0090902"}


id: GO:0071670
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a smooth muscle cell in response to an external stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smooth muscle cell migration","termid":"GO:0014909"},{"relation_name":"is_a","term_name":"cell chemotaxis","termid":"GO:0060326"}],"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":"smooth muscle cell chemotaxis","termid":"GO:0071670"}


id: GO:0006486
data:
  {"annotated_genes":["SJAG_03790","SJAG_01021","SJAG_03764","SJAG_00831","SJAG_02783","SJAG_03555","SJAG_03082","SJAG_01264","SJAG_01950","SJAG_00394","SJAG_01972","SJAG_05219","SJAG_01595","SJAG_00924","SJAG_02163","SJAG_03774","SJAG_01006","SJAG_01491","SJAG_03333","SJAG_01069","SJAG_00598","SJAG_04090","SJAG_02648","SJAG_04906","SJAG_03676","SJAG_02056","SJAG_03656","SJAG_02102","SJAG_00334","SJAG_03149","SJAG_03188","SJAG_03056","SJAG_03150","SJAG_00816","SJAG_04363","SJAG_04401","SJAG_03871","SJAG_05348","SJAG_04770","SJAG_04095","SJAG_01276","SJAG_00747","SJAG_04231","SJAG_00554","SJAG_00183","SJAG_04821","SJAG_04954","SJAG_03311","SJAG_01389","SJAG_04728","SJAG_04127","SJAG_02903","SJAG_02519","SJAG_04316","SJAG_03330","SJAG_02996","SJAG_00437","SJAG_04053","SJAG_03032","SJAG_04952","SJAG_04571"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58990,64118,64422,68138,70202,73821,76200,77196,97608,101953,110355,115954,119837],"is_not":false,"summary":null,"term":"GO:0006486"},{"annotations":[95783,101703,93005,78624,70730,74881,78995,76596,62340,106955,113073,101915,65431,64338,66861,81803],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006488"},{"annotations":[81118,77113,75404,81696,112685,76575,80129,79789,76447,78745,77591,79297,112691,80984,71812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006487"},{"annotations":[81326,78183,81036,100695,102252,120070,100693,80663,100694,89357,76190,71503,100692,59934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018279"},{"annotations":[79298,112686,81119,76576,112692,120071,63925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006493"},{"annotations":[103474,107919,94917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035269"}]},"cv_name":"biological_process","definition":"A protein modification process that results in the addition of a carbohydrate or carbohydrate derivative unit to a protein amino acid, e.g. the addition of glycan chains to proteins.","definition_xrefs":["GOC:curators","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"},{"relation_name":"is_a","term_name":"macromolecule glycosylation","termid":"GO:0043413"},{"relation_name":"part_of","term_name":"glycoprotein biosynthetic process","termid":"GO:0009101"}],"gene_count":61,"genes_by_uniquename":{"SJAG_00183":null,"SJAG_00334":null,"SJAG_00394":null,"SJAG_00437":null,"SJAG_00554":null,"SJAG_00598":null,"SJAG_00747":null,"SJAG_00816":null,"SJAG_00831":null,"SJAG_00924":null,"SJAG_01006":null,"SJAG_01021":null,"SJAG_01069":null,"SJAG_01264":null,"SJAG_01276":null,"SJAG_01389":null,"SJAG_01491":null,"SJAG_01595":null,"SJAG_01950":null,"SJAG_01972":null,"SJAG_02056":null,"SJAG_02102":null,"SJAG_02163":null,"SJAG_02519":null,"SJAG_02648":null,"SJAG_02783":null,"SJAG_02903":null,"SJAG_02996":null,"SJAG_03032":null,"SJAG_03056":null,"SJAG_03082":null,"SJAG_03149":null,"SJAG_03150":null,"SJAG_03188":null,"SJAG_03311":null,"SJAG_03330":null,"SJAG_03333":null,"SJAG_03555":null,"SJAG_03656":null,"SJAG_03676":null,"SJAG_03764":null,"SJAG_03774":null,"SJAG_03790":null,"SJAG_03871":null,"SJAG_04053":null,"SJAG_04090":null,"SJAG_04095":null,"SJAG_04127":null,"SJAG_04231":null,"SJAG_04316":null,"SJAG_04363":null,"SJAG_04401":null,"SJAG_04571":null,"SJAG_04728":null,"SJAG_04770":null,"SJAG_04821":null,"SJAG_04906":null,"SJAG_04952":null,"SJAG_04954":null,"SJAG_05219":null,"SJAG_05348":null},"genotype_count":0,"in_subsets":["bp_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein glycosylation","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0065006"],"synonyms":[{"name":"protein amino acid glycosylation","type":"exact"},{"name":"protein-carbohydrate complex assembly","type":"related"}],"termid":"GO:0006486","terms_by_termid":{"GO:0006486":null,"GO:0006487":null,"GO:0006488":null,"GO:0006493":null,"GO:0018279":null,"GO:0035269":null}}


id: CHEBI:22907
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bleomycin","termid":"CHEBI:22907"}


id: GO:0060756
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Behavior by which an organism locates food.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavior","termid":"GO:0007610"}],"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":"foraging behavior","termid":"GO:0060756"}


id: PBO:0000659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ENTH/VHS domain protein (predicted)","termid":"PBO:0000659"}


id: PR:Q92338
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- abc1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q92338"],"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":"protein ABC1 homolog, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2D10.18","synonyms":[{"name":"Spom972h-abc1","type":"exact"}],"termid":"PR:Q92338"}


id: MONDO:0007210
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":"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay","secondary_identifiers":["MESH:C566206","OMIM:112370","UMLS:C1862171","MEDGEN:396307"],"synonyms":[{"name":"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay","type":"exact"}],"termid":"MONDO:0007210","xrefs":{"Monarch":{"xref_id":"0007210"}}}


id: GO:0102384
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 19-O-beta-glucopyranosyl-steviol + UDP-alpha-D-glucose = rubusoside + UDP + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 19-O-beta-glucopyranosyl-steviol glucosyltransferase activity (obsolete GO:0102384)","termid":"GO:0102384"}


id: PBO:0060756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B4","termid":"PBO:0060756"}


id: GO:0086029
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the transfer of information from a Purkinje myocyte to a ventricular cardiac muscle cell.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling involved in cardiac conduction","termid":"GO:0086019"},{"relation_name":"is_a","term_name":"Purkinje myocyte to ventricular cardiac muscle cell communication","termid":"GO:0086068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"Purkinje myocyte to ventricular cardiac muscle cell signaling","synonyms":[{"name":"Purkinje myocyte to ventricular cardiac muscle cell signalling","type":"exact"}],"termid":"GO:0086029"}


id: PR:P87027
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spg1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87027"],"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":"septum-promoting GTP-binding protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1565.06c","synonyms":[{"name":"GTPase spg1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-spg1","type":"exact"},{"name":"sid3 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87027"}


id: MONDO:0007903
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Li-Fraumeni syndrome 1 (obsolete MONDO:0007903)","termid":"MONDO:0007903","xrefs":{"Monarch":{"xref_id":"0007903"}}}


id: GO:0071554
data:
  {"annotated_genes":["SJAG_04666","SJAG_01888","SJAG_02519","SJAG_04851","SJAG_04771","SJAG_01835","SJAG_04462","SJAG_02916","SJAG_01021","SJAG_01276","SJAG_02192","SJAG_03753","SJAG_04659","SJAG_04668","SJAG_04184","SJAG_01227","SJAG_02278","SJAG_02222","SJAG_01774","SJAG_01181","SJAG_03631","SJAG_00974","SJAG_01264","SJAG_03705","SJAG_03444","SJAG_00424","SJAG_03646","SJAG_04595","SJAG_05272","SJAG_04236","SJAG_02446","SJAG_04483","SJAG_02649","SJAG_04770","SJAG_03295","SJAG_00667","SJAG_04551","SJAG_05001","SJAG_00610","SJAG_02718","SJAG_02468","SJAG_00310","SJAG_01787","SJAG_03082","SJAG_03188","SJAG_04522","SJAG_03057","SJAG_04868","SJAG_01028","SJAG_01171","SJAG_01255","SJAG_05285","SJAG_04864","SJAG_02258","SJAG_03704","SJAG_04073","SJAG_03655","SJAG_02684","SJAG_01017","SJAG_01290","SJAG_00816","SJAG_03123","SJAG_01963","SJAG_02733","SJAG_03483","SJAG_01453","SJAG_04327","SJAG_00163","SJAG_01288","SJAG_04620","SJAG_04906","SJAG_00598","SJAG_02727","SJAG_03013","SJAG_04238","SJAG_01426","SJAG_00876","SJAG_01321","SJAG_00218","SJAG_04878","SJAG_02845","SJAG_00661","SJAG_03587","SJAG_04850","SJAG_02590"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96352],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034413"},{"annotations":[90072,93654,92118,90566],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030476"},{"annotations":[74759],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034412"},{"annotations":[116079,119801,119793,111043,106104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070591"},{"annotations":[82219,79791,76449,76578,81121,79300,73768,78748,89354],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000032"},{"annotations":[95904,102072],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044347"},{"annotations":[80554,72388,75287,75115,73175],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070600"},{"annotations":[117822,115155,108058,93480,76281,74762,77632,72816],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071970"},{"annotations":[104574,80002],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070880"},{"annotations":[110031,103875,97003,103874],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070879"},{"annotations":[71953,95216,72294,76782,102546,81171,73123,97154,119919,72454,104386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009272"},{"annotations":[90963,90139,95906,103876,103877,110032,113302,102073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904541"},{"annotations":[82033,81346,79689,73086,77631,79673,78207,77047,72851,76280,78576,104387,76947,91204,72815,112026],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031505"},{"annotations":[119469,94144,91602,64610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071852"},{"annotations":[108650,74282],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071966"},{"annotations":[104078,112963],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903340"},{"annotations":[89369,94302],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0140748"},{"annotations":[107867,69405,92643,107293,119921,94286,120054],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090334"},{"annotations":[75909,109573,110413,112082],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903338"},{"annotations":[104782,94308,91309,96839],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0070610"},{"annotations":[67913,104081,102105],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032995"},{"annotations":[89452,112964,73303],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0060237"}]},"cv_name":"biological_process","definition":"A process that results in the biosynthesis of constituent macromolecules, assembly, arrangement of constituent parts, or disassembly of a cell wall.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular 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wall organization or biogenesis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0070882"],"synonyms":[{"name":"cell wall organisation or biogenesis","type":"exact"},{"name":"cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"cellular cell wall organisation or biogenesis","type":"exact"},{"name":"cellular cell wall organization or biogenesis","type":"exact"}],"termid":"GO:0071554","terms_by_termid":{"GO:0000032":null,"GO:0009272":null,"GO:0030476":null,"GO:0031505":null,"GO:0032995":null,"GO:0034412":null,"GO:0034413":null,"GO:0044347":null,"GO:0060237":null,"GO:0070591":null,"GO:0070600":null,"GO:0070610":null,"GO:0070879":null,"GO:0070880":null,"GO:0071852":null,"GO:0071966":null,"GO:0071970":null,"GO:0090334":null,"GO:0140748":null,"GO:1903338":null,"GO:1903340":null,"GO:1904541":null}}


id: PBO:0089602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear import protein Nxt2","termid":"PBO:0089602"}


id: PBO:0003442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anamorsin family protein, involved in iron-sulphur cluster assembly (predicted)","termid":"PBO:0003442"}


id: PBO:0031058
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_mixed_population_including_spores_and_divided_germinated_spores_(obsolete_FYPO:0000319)","termid":"PBO:0031058"}


id: GO:0070738
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the posttranslational transfer of one or more glycine residues to a specific glutamate residue on a target tubulin molecule; acts on alpha or beta tubulin.","definition_xrefs":["GOC:mah","PMID:19524510"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-glycine ligase activity","termid":"GO:0070735"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"tubulin-glycine ligase activity","synonyms":[{"name":"tubulin glycylase activity","type":"exact"}],"termid":"GO:0070738"}


id: PBO:0030787
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-aseptate","termid":"PBO:0030787"}


id: PBO:0078588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 60 pseudogene 1, Y-linked","termid":"PBO:0078588"}


id: PBO:0088902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi UDP-galactose transmembrane transporter Gms2","termid":"PBO:0088902"}


id: PBO:0040292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1","termid":"PBO:0040292"}


id: GO:0031643
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the formation of a myelin sheath around nerve axons.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of myelination","termid":"GO:0031641"},{"relation_name":"is_a","term_name":"positive regulation of nervous system process","termid":"GO:0031646"},{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"positively_regulates","term_name":"myelination","termid":"GO:0042552"}],"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 myelination","synonyms":[{"name":"activation of myelination","type":"narrow"},{"name":"stimulation of myelination","type":"narrow"},{"name":"up regulation of myelination","type":"exact"},{"name":"up-regulation of myelination","type":"exact"},{"name":"upregulation of myelination","type":"exact"}],"termid":"GO:0031643"}


id: FYPO:0006320
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 increase in small deletions or duplications (\\\"replication slippage\\\") that normally results from processing arrested replication forks is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:29215009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal replication slippage during replication fork processing","synonyms":[{"name":"normal replication slippage during replication fork processing during vegetative growth","type":"related"},{"name":"normal replication slippage during replication fork processing during vegetative growth during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006320"}


id: PATO:0000217
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000217 immune function (obsolete PATO:0000217)","termid":"PATO:0000217"}


id: GO:0072692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Repression of transcription of DNA at the central core of a regional centromere by altering the structure of chromatin.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete chromatin silencing at centromere central core (obsolete GO:0072692)","synonyms":[{"name":"centromere central core chromatin silencing","type":"exact"},{"name":"chromatin silencing at centromeric central core","type":"exact"},{"name":"chromatin silencing at chromosome kinetochore domain","type":"exact"},{"name":"heterochromatic silencing at centromere central core","type":"exact"}],"termid":"GO:0072692"}


id: GO:0030144
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-glucosamine + N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl-R = UDP + N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl-R. Only branched mannose glycopeptides with non-reducing N-acetylglucosamine terminal residues act as acceptors.","definition_xrefs":["EC:2.4.1.155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a glycoprotein","termid":"GO:0140103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016740","GO:0016757","GO:0140096","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase activity","secondary_identifiers":["Reactome:R-HSA-9696980","MetaCyc:2.4.1.155-RXN","RHEA:16921","Reactome:R-HSA-975916"],"synonyms":[{"name":"GnTV activity","type":"related"},{"name":"N-acetylglucosaminyltransferase V activity","type":"related"},{"name":"UDP-N-acetyl-D-glucosamine:6-[2-(N-acetyl-beta-D-glucosaminyl)-alpha-D-mannosyl]-glycoprotein 6-beta-N-acetyl-D-glucosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetylglucosamine:alpha-mannoside-beta-1,6 N-acetylglucosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetylglucosamine:alpha-mannoside-beta1,6 N-acetylglucosaminyltransferase activity","type":"related"},{"name":"alpha-1,3(6)-mannosylglycoprotein beta-1,6-N-acetylglucosaminyltransferase activity","type":"exact"},{"name":"alpha-1,6-mannosyl-glycoprotein 6-beta-N-acetylglucosaminyltransferase activity","type":"exact"},{"name":"alpha-mannoside beta-1,6-N-acetylglucosaminyltransferase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-alpha-mannoside beta-1->6-acetylglucosaminyltransferase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-alpha-mannoside beta1->6-acetylglucosaminyltransferase activity","type":"related"}],"termid":"GO:0030144"}


id: MONDO:0001371
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A nutritional deficit that is caused by inadequate protein or calorie intake.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nutritional deficiency disease","termid":"MONDO:0006873"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-energy malnutrition","secondary_identifiers":["EFO:0009563","ICD9:263.9","MESH:D011502","ICD9:263.8","DOID:11801","SCTID:238107002","UMLS:C0033677","ICD9:269.8","NCIT:C34952","MEDGEN:19521"],"synonyms":[{"name":"Protein energy malnutrition","type":"exact"}],"termid":"MONDO:0001371","xrefs":{"Monarch":{"xref_id":"0001371"}}}


id: MONDO:0009437
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bamforth-Lazarus syndrome is a very rare syndrome of congenital hypothyroidism characterized by thyroid dysgenesis (in most cases athyreosis), cleft palate and spiky hair, with or without choanal atresia, and bifid epiglottis. Facial dysmorphism and porencephaly have been reported in isolated cases.","definition_xrefs":["Orphanet:1226"],"direct_ancestors":[{"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":"endocrine system disorder","termid":"MONDO:0005151"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bamforth-Lazarus syndrome","secondary_identifiers":["SCTID:722375007","DOID:0050655","MESH:C537901","UMLS:C1855794","GARD:414","MEDGEN:343420","OMIM:241850","icd11.foundation:1747690671"],"synonyms":[{"name":"Athyroidal hypothyroidism-spiky hair-cleft palate syndrome","type":"exact"},{"name":"Bamforth syndrome","type":"exact"},{"name":"Bamforth-Lazarus syndrome","type":"exact"},{"name":"hypothyroidism cleft palate hypothyroidism, athyroidal, with spiky hair and cleft palate","type":"related"},{"name":"hypothyroidism, ATHYROIDAL, with spiky hair and cleft palate","type":"exact"},{"name":"hypothyroidism, thyroidal or ATHYROIDAL, with spiky hair and cleft palate","type":"related"},{"name":"hypothyroidism-cleft palate syndrome","type":"exact"}],"termid":"MONDO:0009437","xrefs":{"Monarch":{"xref_id":"0009437"}}}


id: PBO:0064537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POM121 transmembrane nucleoporin","termid":"PBO:0064537"}


id: GO:0000276
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. All non-F1 subunits of the mitochondrial hydrogen-transporting ATP synthase, including integral and peripheral mitochondrial inner membrane proteins.","definition_xrefs":["PMID:10838056","GOC:mtg_sensu"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial proton-transporting ATP synthase complex, coupling factor F(o) (obsolete GO:0000276)","termid":"GO:0000276"}


id: PBO:0027979
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_level_during_cellular_response_to_cadmium_ion","termid":"PBO:0027979"}


id: MONDO:0859336
data:
  {"annotated_genes":["SJAG_04513"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87421],"is_not":false,"summary":null,"term":"MONDO:0859336"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04513":null},"genotype_count":0,"is_obsolete":false,"name":"muscular dystrophy, congenital, with or without seizures","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5774274","MEDGEN:1824047","OMIM:620166"],"termid":"MONDO:0859336","terms_by_termid":{"MONDO:0859336":null},"xrefs":{"Monarch":{"xref_id":"0859336"}}}


id: MONDO:0017006
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete X and Y chromosomal anomaly (obsolete MONDO:0017006)","secondary_identifiers":["Orphanet:263749"],"termid":"MONDO:0017006","xrefs":{"Monarch":{"xref_id":"0017006"}}}


id: PBO:0042844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 52","termid":"PBO:0042844"}


id: MONDO:0008593
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":"trichomegaly","secondary_identifiers":["OMIM:190330","UMLS:C0854699","MEDGEN:163139"],"synonyms":[{"name":"TCMGLY","type":"related"},{"name":"eyelashes, long","type":"related"},{"name":"trichomegaly","type":"exact"}],"termid":"MONDO:0008593","xrefs":{"Monarch":{"xref_id":"0008593"}}}


id: PBO:0081714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 639","termid":"PBO:0081714"}


id: MOD:01524
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"The protein modification reporter fragment produced by an Applied Biosystems iTRAQ4plex 116 reagent derivatized residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"iTRAQ4plex-116 reporter+balance reagent acylated residue","termid":"MOD:01499"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter fragment","termid":"MOD:01521"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ4plex-116 reporter fragment","synonyms":[{"name":"4-methyl-1-methylidenepiperazin-1-ium","type":"exact"}],"termid":"MOD:01524"}


id: PBO:0045403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPPA3 pseudogene 5","termid":"PBO:0045403"}


id: MONDO:0800446
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, isolated constitutional thrombocytopenia disease characterized by impaired platelet aggregation resulting from a defect in thromboxane synthesis or signaling, manifesting with mild to moderate mucocutaneous, gastrointestinal or surgical bleeding (e.g. easy bruising, prolonged epistaxis, excessive bleeding after a tooth extraction).","definition_xrefs":["Orphanet:220443"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"}],"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":"bleeding diathesis due to thromboxane synthesis deficiency","secondary_identifiers":["icd11.foundation:1676860885","UMLS:C5190857","MEDGEN:1678745","GARD:17132"],"termid":"MONDO:0800446","xrefs":{"Monarch":{"xref_id":"0800446"}}}


id: PBO:0083551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps verfied gene PMT5/YDL093W; YDL094C is not essential","termid":"PBO:0083551"}


id: GO:0018343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The covalent attachment of a farnesyl group to a protein.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein prenylation","termid":"GO:0018342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein farnesylation","secondary_identifiers":["GO:0018347"],"synonyms":[{"name":"C-terminal protein farnesylation","type":"narrow"},{"name":"protein amino acid farnesylation","type":"exact"}],"termid":"GO:0018343"}


id: PBO:0078762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase subunit 11-2 pseudogene 5","termid":"PBO:0078762"}


id: PBO:0074216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 44 member 2","termid":"PBO:0074216"}


id: PBO:0073984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 24 member 4","termid":"PBO:0073984"}


id: MONDO:0009150
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome is characterized by alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction (primary hypothyroidism), hypohidrosis, ephelides, enteropathy, and respiratory tract infections due to ciliary dyskinesia, leading to suggestion of the acronym ANother syndrome as alternative name for this condition. It has been described in three patients (two brothers and an unrelated girl). Transmission is autosomal recessive.","definition_xrefs":["Orphanet:1882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome","secondary_identifiers":["GARD:2049","MESH:C565604","SCTID:239050000","UMLS:C1857052","MEDGEN:384046","OMIM:225050"],"synonyms":[{"name":"HEDH syndrome","type":"exact"},{"name":"another syndrome","type":"exact"},{"name":"ectodermal dysplasia hypohidrotic with hypothyroidism and ciliary dyskinesia","type":"related"},{"name":"ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia","type":"related"},{"name":"hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia","type":"related"},{"name":"hypohidrotic ectodermal dysplasia with hypothyroidism","type":"related"},{"name":"hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia","type":"related"}],"termid":"MONDO:0009150","xrefs":{"Monarch":{"xref_id":"0009150"}}}


id: MONDO:0009919
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy.","definition_xrefs":["Orphanet:2971"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of peroxisomal beta oxidation","termid":"MONDO:0019233"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019053"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0019053"],"is_obsolete":false,"name":"peroxisomal acyl-CoA oxidase deficiency","secondary_identifiers":["DOID:0050797","NCIT:C170437","NANDO:1200765","OMIM:264470","icd11.foundation:927825451","ICD9:255.41","MEDGEN:376636","MESH:C536662","SCTID:238069004","UMLS:C1849678","GARD:4543"],"synonyms":[{"name":"ACOX1 deficiency","type":"exact"},{"name":"Pseudoadrenoleukodystrophy","type":"exact"},{"name":"Pseudoneonatal adrenoleukodystrophy","type":"related"},{"name":"peroxisomal acyl-CoA oxidase deficiency","type":"exact"},{"name":"peroxisomal acyl-coenzyme A oxidase","type":"exact"},{"name":"pseudo-NALD","type":"exact"},{"name":"pseudo-neonatal adrenoleukodystrophy","type":"exact"},{"name":"straight-chain acyl-Coa oxidase deficiency","type":"related"}],"termid":"MONDO:0009919","xrefs":{"Monarch":{"xref_id":"0009919"}}}


id: PBO:0066249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMS3 antisense RNA 2","termid":"PBO:0066249"}


id: MONDO:0003502
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare squamous cell carcinoma that arises from the ureter.","definition_xrefs":["NCIT:C6154"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"ureter carcinoma","termid":"MONDO:0006481"}],"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":"ureter squamous cell carcinoma","secondary_identifiers":["MEDGEN:237032","UMLS:C1336879","DOID:5539"],"synonyms":[{"name":"epidermoid carcinoma of the ureter","type":"exact"},{"name":"epidermoid carcinoma of ureter","type":"exact"},{"name":"squamous cell carcinoma of the ureter","type":"exact"},{"name":"squamous cell carcinoma of ureter","type":"exact"},{"name":"ureter epidermoid carcinoma","type":"exact"},{"name":"ureter squamous cell carcinoma","type":"exact"},{"name":"ureteral epidermoid carcinoma","type":"exact"},{"name":"ureteral squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0003502","xrefs":{"Monarch":{"xref_id":"0003502"}}}


id: PBO:0061889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OPCML intronic transcript 2","termid":"PBO:0061889"}


id: PBO:0027835
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_septum_disassembly","termid":"PBO:0027835"}


id: MONDO:0009327
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"congenital heart malformation","termid":"MONDO:0019512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heart, malformation of","secondary_identifiers":["OMIM:140500","OMIM:234750"],"synonyms":[{"name":"heart, malformation of","type":"exact"}],"termid":"MONDO:0009327","xrefs":{"Monarch":{"xref_id":"0009327"}}}


id: MONDO:0017556
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Madelung deformity","termid":"MONDO:0018154"}],"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":"Madelung deformity, unilateral","secondary_identifiers":["icd11.foundation:1964514438","Orphanet:295221"],"termid":"MONDO:0017556","xrefs":{"Monarch":{"xref_id":"0017556"}}}


id: PR:O74520
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trp663 gene.","definition_xrefs":["UniProtKB:O74520","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 membrane protein C663.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC663.14c","synonyms":[{"name":"Spom972h-trp663","type":"exact"}],"termid":"PR:O74520"}


id: PBO:0088616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial outer membrane protein, TspO/MBR-related, implicated in lipid/sterol transport, tspO","termid":"PBO:0088616"}


id: PBO:0044456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily F member 35, pseudogene","termid":"PBO:0044456"}


id: PBO:0048835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein nucleolar 2 pseudogene 1","termid":"PBO:0048835"}


id: PBO:0002104
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DRE Element Binding","termid":"PBO:0002104"}


id: PBO:0051423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 2-34 (pseudogene)","termid":"PBO:0051423"}


id: GO:0018229
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a C-terminal peptidyl-cysteine to form peptidyl-L-cysteine methyl ester.","definition_xrefs":["RESID:AA0105"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-L-cysteine methyl ester biosynthetic process from peptidyl-cysteine (obsolete GO:0018229)","synonyms":[{"name":"peptidyl-L-cysteine methyl ester anabolism from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-L-cysteine methyl ester formation from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-L-cysteine methyl ester synthesis from peptidyl-cysteine","type":"exact"}],"termid":"GO:0018229"}


id: GO:0003115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of reductions in the diameter of blood vessels as a result of secretion of epinephrine into the bloodstream or released by nerve endings.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vasoconstriction","termid":"GO:0019229"}],"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 vasoconstriction by epinephrine","termid":"GO:0003115"}


id: PBO:0084189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Histone H2A; core histone protein required for chromatin assembly and chromosome function; one of two nearly identical (see also HTA1) subtypes; DNA damage-dependent phosphorylation by Mec1p facilitates DNA repair; acetylated by Nat4p","termid":"PBO:0084189"}


id: PR:Q9Y7T0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DnaJ homolog subfamily C member 11 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04469"],"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 J domain-containing protein C63.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC63.03","secondary_identifiers":["UniProtKB:Q9Y7T0"],"synonyms":[{"name":"Spom972h-DNAJC11","type":"exact"}],"termid":"PR:Q9Y7T0"}


id: GO:0034644
data:
  {"annotated_genes":["SJAG_01262","SJAG_05197","SJAG_02200","SJAG_00814","SJAG_01010","SJAG_03898","SJAG_00272","SJAG_02334","SJAG_01648","SJAG_02828","SJAG_02182","SJAG_00863","SJAG_02818","SJAG_04877","SJAG_04190","SJAG_04150","SJAG_00729","SJAG_00208","SJAG_02199"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78653,111079,97139,104761],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[70512,71793,66022,97920,106164,107896,114822,95543,66914,99034,77439,89869,67868,60750,69013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070914"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an ultraviolet radiation (UV light) stimulus. Ultraviolet radiation is electromagnetic radiation with a wavelength in the range of 10 to 380 nanometers.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to UV","termid":"GO:0009411"},{"relation_name":"is_a","term_name":"cellular response to light stimulus","termid":"GO:0071482"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00208":null,"SJAG_00272":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00863":null,"SJAG_01010":null,"SJAG_01262":null,"SJAG_01648":null,"SJAG_02182":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02334":null,"SJAG_02818":null,"SJAG_02828":null,"SJAG_03898":null,"SJAG_04150":null,"SJAG_04190":null,"SJAG_04877":null,"SJAG_05197":null},"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 UV","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"cellular response to UV light stimulus","type":"exact"},{"name":"cellular response to UV radiation stimulus","type":"exact"},{"name":"cellular response to ultraviolet light stimulus","type":"exact"},{"name":"cellular response to ultraviolet radiation stimulus","type":"exact"}],"termid":"GO:0034644","terms_by_termid":{"GO:0070914":null,"GO:1904161":null}}


id: PBO:0049696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan and proteoglycan link protein 2","termid":"PBO:0049696"}


id: FYPO:0004640
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of CAAX-protein geranylgeranyltransferase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000654","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"abnormal CAAX-protein geranylgeranyltransferase activity","termid":"FYPO:0004640"}


id: PBO:0090718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome base subcomplex ATPase subunit Rpt3","termid":"PBO:0090718"}


id: MONDO:0007191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.","definition_xrefs":["Orphanet:117"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete predominantly large-vessel vasculitis (obsolete MONDO:0015488)","termid":"MONDO:0015488"},{"relation_name":"excluded_subClassOf","term_name":"obsolete inflammatory and autoimmune disease with epilepsy (obsolete MONDO:0015657)","termid":"MONDO:0015657"},{"relation_name":"excluded_subClassOf","term_name":"obsolete systemic diseases with anterior uveitis (obsolete MONDO:0017259)","termid":"MONDO:0017259"},{"relation_name":"excluded_subClassOf","term_name":"obsolete systemic diseases with posterior uveitis (obsolete MONDO:0017260)","termid":"MONDO:0017260"},{"relation_name":"excluded_subClassOf","term_name":"obsolete systemic diseases with panuveitis (obsolete MONDO:0017261)","termid":"MONDO:0017261"},{"relation_name":"excluded_subClassOf","term_name":"obsolete autoinflammatory syndrome with skin involvement (obsolete MONDO:0017370)","termid":"MONDO:0017370"},{"relation_name":"excluded_subClassOf","term_name":"obsolete unclassified autoinflammatory syndrome (obsolete MONDO:0017957)","termid":"MONDO:0017957"},{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"skin vascular disease","termid":"MONDO:0019293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"Behcet disease","secondary_identifiers":["NCIT:C34416","OMIM:109650","DOID:13241","SCTID:310701003","UMLS:C0004943","ICD9:136.1","GARD:848","NANDO:1200284","NANDO:2200422","MEDGEN:2568","icd11.foundation:1668927157","MedDRA:10004213","MESH:D001528","EFO:0003780"],"synonyms":[{"name":"Adamantiades-Behcet disease","type":"exact"},{"name":"BD","type":"related"},{"name":"Bechet syndrome","type":"exact"},{"name":"Behcet disease","type":"exact"},{"name":"Behcet syndrome","type":"exact"},{"name":"Behcet's disease","type":"related"},{"name":"Behcet's syndrome","type":"exact"},{"name":"Behet's syndrome","type":"exact"},{"name":"Behçet disease","type":"exact"},{"name":"Behçet syndrome","type":"exact"},{"name":"Behçet's disease","type":"related"},{"name":"Behçet's syndrome","type":"exact"},{"name":"Behçet-Adamantiades syndrome","type":"exact"},{"name":"Behçet’s disease","type":"related"},{"name":"Morbus Behçet's syndrome","type":"exact"},{"name":"silk road disease","type":"exact"},{"name":"triple symptom complex","type":"exact"}],"termid":"MONDO:0007191","xrefs":{"Monarch":{"xref_id":"0007191"}}}


id: MONDO:0100245
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acquired paroxysmal nocturnal hemoglobinuria (obsolete MONDO:0100245)","termid":"MONDO:0100245","xrefs":{"Monarch":{"xref_id":"0100245"}}}


id: MONDO:0006633
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the gallbladder in the absence of gallstones.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholecystitis","termid":"MONDO:0002155"},{"relation_name":"is_a","term_name":"cystitis","termid":"MONDO:0006032"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"acalculous cholecystitis","secondary_identifiers":["SCTID:19968009","DOID:2828","MedDRA:10000347","MEDGEN:82762","UMLS:C0267841","NCIT:C35578","EFO:1000790","MESH:D042101"],"synonyms":[{"name":"acute acalculous cholecystitis","type":"narrow"},{"name":"acute cholecystitis without calculus","type":"exact"},{"name":"cholecystitis without calculus","type":"exact"}],"termid":"MONDO:0006633","xrefs":{"Monarch":{"xref_id":"0006633"}}}


id: PBO:0082791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Trk1p-Trk2p potassium transport system; contributes to K(+) supply and maintenance of plasma-membrane potential; TRK2 has a paralog, TRK1, that arose from the whole genome duplication","termid":"PBO:0082791"}


id: PBO:0031177
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitotic_catastrophe,_small_cell","termid":"PBO:0031177"}


id: MONDO:1012623
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any X-linked tremor that occurs in dogs due to a mutation in the PLP1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tremor, dog","termid":"MONDO:1012279"},{"relation_name":"is_a","term_name":"X-linked disease, non-human animal","termid":"MONDO:1012575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked canine shaking pup, PLP1-related, dog","secondary_identifiers":["OMIA:000770-9615"],"synonyms":[{"name":"SHP","type":"exact"},{"name":"tremor, X-linked, dog","type":"related"}],"termid":"MONDO:1012623","xrefs":{"Monarch":{"xref_id":"1012623"}}}


id: MONDO:0010922
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Satoyoshi syndrome is a rare syndrome characterized by progressive, painful, intermittent muscle spasms. These muscle spasms usually start between 6-15 years old. Other symptoms of the syndrome may include diarrhea and an inability of the digestive tract to absorb certain foods, especially carbohydrates (malabsorption). People affected by Satoyoshi syndrome may also have loss of hair on the head and body (alopecia universalis), short stature, and skeletal abnormalities. Women with Satoyoshi syndrome may not have a menstrual cycle (amenorrhea). In all published cases, only one person in a family has Satoyoshi syndrome. This is even true when the person with Satoyoshi syndrome comes from a large family. Satoyoshi syndrome seems to be more common in Japan. The exact cause of the syndrome is unknown, but some researchers think it may be an autoimmune disease. Satoyoshi syndrome can be diagnosed when a doctor sees symptoms that are consistent with the syndrome. The diagnosis can be confirmed by a variety of laboratory tests. Treatment for Satoyoshi syndrome includes medication to suppress the immune system.","direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia","termid":"MONDO:0004907"},{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005047"],"is_obsolete":false,"name":"Satoyoshi syndrome","secondary_identifiers":["SCTID:763630007","MedDRA:10070579","GARD:160","UMLS:C1833454","Orphanet:3130","OMIM:600705","MESH:C536616","MEDGEN:318882"],"synonyms":[{"name":"Komuragaeri disease","type":"exact"},{"name":"Satoyoshi syndrome","type":"exact"},{"name":"muscle spasms, intermittent with alopecia, diarrhea and skeletal abnormalities","type":"related"},{"name":"muscle spasms, intermittent with alopecia, diarrhoea and skeletal abnormalities","type":"related"},{"name":"muscle spasms, intermittent, with alopecia, diarrhea, and skeletal abnormalities","type":"related"}],"termid":"MONDO:0010922","xrefs":{"Monarch":{"xref_id":"0010922"}}}


id: PBO:0116790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholesin","termid":"PBO:0116790"}


id: PBO:0027877
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_nucleosome_binding","termid":"PBO:0027877"}


id: PBO:0030295
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cell-substrate_adhesion","termid":"PBO:0030295"}


id: GO:0033179
data:
  {"annotated_genes":["SJAG_05294","SJAG_00516","SJAG_02782","SJAG_03406","SJAG_03962","SJAG_01913","SJAG_02023"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[105841,62670,97550,92030,101865,93934,97731],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000220"}]},"cv_name":"cellular_component","definition":"A protein complex that forms part of a proton-transporting V-type ATPase and mediates proton transport across a membrane. The V0 complex consists of at least four different subunits (a,c,d and e); six or more c subunits form a proton-binding rotor ring.","definition_xrefs":["ISBN:0716743663","PMID:16449553","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton-transporting two-sector ATPase complex, proton-transporting domain","termid":"GO:0033177"},{"relation_name":"part_of","term_name":"proton-transporting V-type ATPase complex","termid":"GO:0033176"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00516":null,"SJAG_01913":null,"SJAG_02023":null,"SJAG_02782":null,"SJAG_03406":null,"SJAG_03962":null,"SJAG_05294":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"proton-transporting V-type ATPase, V0 domain","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"termid":"GO:0033179","terms_by_termid":{"GO:0000220":null}}


id: MONDO:1012235
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Kidney disorder that occurs in dogs.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal disease, non-human animal","termid":"MONDO:1011909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"renal disease, dog","secondary_identifiers":["OMIA:000856-9615"],"termid":"MONDO:1012235","xrefs":{"Monarch":{"xref_id":"1012235"}}}


id: GO:0001765
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a membrane raft, a small (10-200 nm), heterogeneous, highly dynamic, sterol- and sphingolipid-enriched membrane domains that compartmentalizes cellular processes.","definition_xrefs":["PMID:16645198","PMID:12803918","PMID:12648772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane raft organization","termid":"GO:0031579"},{"relation_name":"is_a","term_name":"membrane assembly","termid":"GO:0071709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0061024"],"is_obsolete":false,"name":"membrane raft assembly","synonyms":[{"name":"lipid raft assembly","type":"exact"},{"name":"lipid raft formation","type":"related"},{"name":"membrane raft formation","type":"related"}],"termid":"GO:0001765"}


id: MONDO:0020487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pontiac fever (PF) is a mild form of legionellosis manifesting with flu-like symptoms such as nausea, myalgia, fever, cough and headache but without pneumonia.","definition_xrefs":["Orphanet:99748"],"direct_ancestors":[{"relation_name":"is_a","term_name":"legionellosis","termid":"MONDO:0005823"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pontiac fever","secondary_identifiers":["DOID:0050150","UMLS:C0343528","MedDRA:10054161","MEDGEN:575661","NCIT:C128335","icd11.foundation:1670562980","GARD:13588","ICD9:041.89","SCTID:240447002"],"termid":"MONDO:0020487","xrefs":{"Monarch":{"xref_id":"0020487"}}}


id: GO:0009879
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment of an organism's body plan or a part of an organism such that it is symmetric around a central axis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of symmetry","termid":"GO:0009799"},{"relation_name":"part_of","term_name":"radial pattern formation","termid":"GO:0009956"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"determination of radial symmetry","synonyms":[{"name":"determination of radial asymmetry","type":"exact"}],"termid":"GO:0009879"}


id: PR:P41887
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A heat shock protein HSP 90-alpha that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01614","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein 90 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC926.04c","secondary_identifiers":["UniProtKB:P41887"],"synonyms":[{"name":"Spom972h-HSP90AA1","type":"exact"}],"termid":"PR:P41887"}


id: MONDO:0002412
data:
  {"annotated_genes":["SJAG_02107","SJAG_02369","SJAG_03660","SJAG_03149","SJAG_03824","SJAG_02131","SJAG_02009","SJAG_00461","SJAG_00605","SJAG_03150","SJAG_02785"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86979,86980,86981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013046"},{"annotations":[89093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010392"},{"annotations":[87667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009865"},{"annotations":[87051,87052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009290"},{"annotations":[87503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009295"},{"annotations":[89073,89074],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013291"},{"annotations":[88067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009867"},{"annotations":[88564,88565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014526"}]},"cv_name":"mondo","definition":"An inherited metabolic disorder characterized either by defects in glycogen synthesis or defects in the breaking down of glycogen. It results either in the creation of abnormal forms of glycogen or accumulation of glycogen in the tissues.","definition_xrefs":["NCIT:C61272"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete inborn glycogen metabolism disorder (obsolete MONDO:0000422)","termid":"MONDO:0000422"},{"relation_name":"is_a","term_name":"inborn carbohydrate metabolic disorder","termid":"MONDO:0019214"},{"relation_name":"is_a","term_name":"inborn disorder of energy metabolism","termid":"MONDO:0019243"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00461":null,"SJAG_00605":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02131":null,"SJAG_02369":null,"SJAG_02785":null,"SJAG_03149":null,"SJAG_03150":null,"SJAG_03660":null,"SJAG_03824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"disorder of glycogen metabolism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18973","ICD10CM:E74.0","ICD9:271.0","MESH:D006008","icd11.foundation:1187107383","DOID:0050728","DOID:2747","MedDRA:10061990","NANDO:1200838","Orphanet:79201","OMIMPS:232200","SCTID:29633007","UMLS:C0017919","MEDGEN:6639"],"synonyms":[{"name":"GSD","type":"exact"},{"name":"glycogen metabolism disorder","type":"exact"},{"name":"glycogen storage disease","type":"exact"},{"name":"glycogen storage disorder","type":"exact"},{"name":"glycogenoses","type":"exact"},{"name":"glycogenosis","type":"exact"},{"name":"inborn error of glycogen metabolic process","type":"exact"},{"name":"inborn glycogen metabolic process disorder","type":"exact"},{"name":"inborn glycogen storage disorder","type":"exact"},{"name":"rare inborn error of glycogen metabolic process","type":"exact"}],"termid":"MONDO:0002412","terms_by_termid":{"MONDO:0009290":null,"MONDO:0009295":null,"MONDO:0009865":null,"MONDO:0009867":null,"MONDO:0010392":null,"MONDO:0013046":null,"MONDO:0013291":null,"MONDO:0014526":null},"xrefs":{"Monarch":{"xref_id":"0002412"}}}


id: PBO:0072298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 16","termid":"PBO:0072298"}


id: PBO:0090849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial tRNA N6-threonyl-carbamoyl-adenosine (t6A) Sua5","termid":"PBO:0090849"}


id: PBO:0005324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial outer membrane ATPase Msp1 (predicted)","termid":"PBO:0005324"}


id: GO:0071009
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A spliceosomal snRNP complex that is formed by the association of the U4atac/U6atac and U5 snRNPs.","definition_xrefs":["GOC:pr","ISBN:0879695897","GOC:krc","PMID:16201866","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal tri-snRNP complex","termid":"GO:0097526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"U4atac/U6atac x U5 tri-snRNP complex","synonyms":[{"name":"U4atac/U6atac.U5 snRNP complex","type":"exact"}],"termid":"GO:0071009"}


id: GO:0120017
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Removes a ceramide from a membrane or a monolayer lipid particle, transports it through the aqueous phase while protected in a hydrophobic pocket, and brings it to an acceptor membrane or lipid particle.","definition_xrefs":["PMID:24220498","PMID:25797198","GOC:krc","PMID:20823909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sphingolipid transfer activity","termid":"GO:0120016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0120013"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0120013"],"is_obsolete":false,"name":"ceramide transfer activity","secondary_identifiers":["GO:0035620"],"synonyms":[{"name":"ceramide carrier activity","type":"exact"},{"name":"ceramide transporter activity","type":"broad"},{"name":"intermembrane ceramide transfer activity","type":"narrow"}],"termid":"GO:0120017"}


id: PBO:0068850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 88, pseudogene","termid":"PBO:0068850"}


id: PBO:0059679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 45","termid":"PBO:0059679"}


id: PBO:0038470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily A member 9","termid":"PBO:0038470"}


id: GO:0015535
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: fucose(out) + H+(out) = fucose(in) + H+(in).","definition_xrefs":["TC:2.A.1.7.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexose:proton symporter activity","termid":"GO:0009679"},{"relation_name":"is_a","term_name":"fucose transmembrane transporter activity","termid":"GO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"fucose:proton symporter activity","secondary_identifiers":["MetaCyc:TRANS-RXN-20","RHEA:29023"],"synonyms":[{"name":"fucose:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015535"}


id: MONDO:0021221
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the vestibulocochlear nerve.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibulocochlear nerve disorder","termid":"MONDO:0001563"},{"relation_name":"is_a","term_name":"cranial nerve neoplasm","termid":"MONDO:0002633"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vestibulocochlear nerve neoplasm","secondary_identifiers":["SCTID:387891008","MEDGEN:91099","NCIT:C5120","UMLS:C0346330"],"synonyms":[{"name":"Vestibuloacoustic nerve neoplasms","type":"exact"},{"name":"acoustic nerve neoplasm","type":"exact"},{"name":"acoustic nerve tumor","type":"exact"},{"name":"acoustic nerve tumour","type":"exact"},{"name":"cranial nerve eight neoplasms","type":"exact"},{"name":"eighth cranial nerve neoplasm","type":"exact"},{"name":"eighth cranial nerve neoplasms","type":"exact"},{"name":"eighth cranial nerve tumor","type":"exact"},{"name":"eighth cranial nerve tumour","type":"exact"},{"name":"neoplasm of acoustic nerve","type":"exact"},{"name":"neoplasm of eighth cranial nerve","type":"exact"},{"name":"neoplasm of the acoustic nerve","type":"exact"},{"name":"neoplasm of the eighth cranial nerve","type":"exact"},{"name":"neoplasm of the vestibulocochlear nerve","type":"exact"},{"name":"neoplasm of vestibulocochlear nerve","type":"exact"},{"name":"tumor of acoustic nerve","type":"exact"},{"name":"tumor of eighth cranial nerve","type":"exact"},{"name":"tumor of the acoustic nerve","type":"exact"},{"name":"tumor of the eighth cranial nerve","type":"exact"},{"name":"tumor of the vestibulocochlear nerve","type":"exact"},{"name":"tumor of vestibulocochlear nerve","type":"exact"},{"name":"tumour of acoustic nerve","type":"exact"},{"name":"tumour of eighth cranial nerve","type":"exact"},{"name":"tumour of the acoustic nerve","type":"exact"},{"name":"tumour of the eighth cranial nerve","type":"exact"},{"name":"tumour of the vestibulocochlear nerve","type":"exact"},{"name":"tumour of vestibulocochlear nerve","type":"exact"},{"name":"vestibulocochlear nerve neoplasm (disease)","type":"exact"},{"name":"vestibulocochlear nerve neoplasms","type":"exact"},{"name":"vestibulocochlear nerve tumor","type":"exact"},{"name":"vestibulocochlear nerve tumour","type":"exact"}],"termid":"MONDO:0021221","xrefs":{"Monarch":{"xref_id":"0021221"}}}


id: PBO:0004462
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Accumulation of Condensin at RDNA","termid":"PBO:0004462"}


id: PBO:0041251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1 open reading frame 167","termid":"PBO:0041251"}


id: PBO:0087515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of heterotrimeric Replication Protein A (RPA); RPA is a highly conserved single-stranded DNA binding protein complex involved in DNA replication, repair, recombination; RPA protects against inappropriate telomere recombination, and upon telomere uncapping, prevents cell proliferation by a checkpoint-independent pathway; with Sgs1p-Top2p-Rmi1p, stimulates DNA catenation/decatenation activity of Top3p; protein abundance increases in response to DNA replication stress","termid":"PBO:0087515"}


id: PBO:0111892
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM domain","termid":"PBO:0111892"}


id: PBO:0067802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 104","termid":"PBO:0067802"}


id: PBO:0061791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"outer dynein arm docking complex subunit 2 pseudogene 1","termid":"PBO:0061791"}


id: PBO:0044671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"damage specific DNA binding protein 2","termid":"PBO:0044671"}


id: GO:0000225
data:
  {"annotated_genes":["SJAG_01416"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72405],"is_not":false,"summary":null,"term":"GO:0000225"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acetyl-D-glucosaminylphosphatidylinositol + H2O = D-glucosaminylphosphatidylinositol + acetate. This reaction is the second step of the biosynthesis of glycosylphosphatidylinositol (GPI), used to anchor various eukaryotic proteins to the cell-surface membrane.","definition_xrefs":["EC:3.5.1.89"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"},{"relation_name":"is_a","term_name":"deacetylase activity","termid":"GO:0019213"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01416":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0016810","GO:0003674","GO:0016787","GO:0019213"],"is_obsolete":false,"name":"N-acetylglucosaminylphosphatidylinositol deacetylase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:11660","Reactome:R-HSA-162857","MetaCyc:3.1.1.69-RXN"],"synonyms":[{"name":"6-(N-acetyl-alpha-D-glucosaminyl)-1-phosphatidyl-1D-myo-inositol acetylhydrolase activity","type":"related"},{"name":"GlcNAc-PI de-N-acetylase activity","type":"related"},{"name":"GlcNAc-PI deacetylase activity","type":"related"},{"name":"N-acetyl-D-glucosaminylphosphatidylinositol acetylhydrolase activity","type":"related"},{"name":"N-acetylglucosaminylphosphatidylinositol de-N-acetylase activity","type":"related"},{"name":"acetylglucosaminylphosphatidylinositol deacetylase activity","type":"related"}],"termid":"GO:0000225","terms_by_termid":{"GO:0000225":null}}


id: GO:0000419
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"RNA polymerase V is a multisubunit RNA polymerase complex found in the nucleus of plants and involved in accumulation of siRNAs and in DNA methylation-dependent silencing of endogenous repeated sequences. Pol V is composed of subunits that are paralogous or identical to the 12 subunits of Pol II. Two large subunits comprise the most conserved portion including the catalytic site and share similarity with other eukaryotic and bacterial multisubunit RNA polymerases. The second largest subunit is also found in RNA polymerase IVa, while the largest subunit is found only in the IVa complex and contains an extended C-terminal domain (CTD) that includes multiple repeats of a 16 amino-acid consensus sequence as well as other sequences. The remainder of the complex is composed of smaller subunits.","definition_xrefs":["PMID:19110459","GOC:krc","PMID:16140984","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear DNA-directed RNA polymerase complex","termid":"GO:0055029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"RNA polymerase V complex","secondary_identifiers":["GO:0080137"],"synonyms":[{"name":"DNA-directed RNA polymerase IVb complex","type":"exact"},{"name":"DNA-directed RNA polymerase V complex","type":"exact"}],"termid":"GO:0000419"}


id: GO:0033077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a T cell via a differentiation pathway dependent upon transit through the thymus.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell differentiation","termid":"GO:0030217"}],"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":"T cell differentiation in thymus","synonyms":[{"name":"T cell development in thymus","type":"related"},{"name":"thymic T cell differentiation","type":"exact"},{"name":"thymocyte cell differentiation","type":"exact"},{"name":"thymocyte differentiation","type":"exact"}],"termid":"GO:0033077"}


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


id: MONDO:1010503
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Endocardial fibroelastosis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocardial fibroelastosis, non-human animal","termid":"MONDO:1010027"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endocardial fibroelastosis, dog","secondary_identifiers":["OMIA:001803-9615"],"termid":"MONDO:1010503","xrefs":{"Monarch":{"xref_id":"1010503"}}}


id: GO:0060629
data:
  {"annotated_genes":["SJAG_02104","SJAG_04457","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95770,112161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090006"},{"annotations":[104323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062123"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of homologous chromosome segregation, the cell cycle process in which replicated homologous chromosomes are organized and then physically separated and apportioned to two sets during the first division of the meiotic cell cycle. Each replicated chromosome, composed of two sister chromatids, aligns at the cell equator, paired with its homologous partner; this pairing off, referred to as synapsis, permits genetic recombination. One homolog (both sister chromatids) of each morphologic type goes into each of the resulting chromosome sets.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chromosome segregation","termid":"GO:0051983"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"homologous chromosome segregation","termid":"GO:0045143"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02104":null,"SJAG_03048":null,"SJAG_04457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of homologous chromosome segregation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0060629","terms_by_termid":{"GO:0062123":null,"GO:0090006":null}}


id: GO:0101014
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: [isocitrate dehydrogenase] phosphate + H2O = [isocitrate dehydrogenase] + phosphate.","definition_xrefs":["PMID:6292732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoprotein phosphatase activity","termid":"GO:0004721"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016787","GO:0004721","GO:0003824","GO:0003674","GO:0016788","GO:0140096"],"is_obsolete":false,"name":"[isocitrate dehydrogenase (NADP+)] phosphatase activity","secondary_identifiers":["MetaCyc:ICITDEHASE-KIN-PHOSPHA"],"synonyms":[{"name":"isocitrate dehydrogenase kinase/phosphatase activity","type":"broad"}],"termid":"GO:0101014"}


id: GO:0070517
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex containing three of the five subunits of eukaryotic replication factor C, those corresponding to human p40, p38, and p37.","definition_xrefs":["PMID:8692848","PMID:9582326","PMID:9228079"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear DNA replication factor C complex","termid":"GO:0043599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"DNA replication factor C core complex","synonyms":[{"name":"RFC core complex","type":"exact"}],"termid":"GO:0070517"}


id: GO:0015323
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mtg_transport"],"gene_count":0,"genotype_count":0,"name":"obsolete type V protein secretor activity (obsolete GO:0015323)","synonyms":[{"name":"type V protein secretor activity","type":"exact"}],"termid":"GO:0015323"}


id: GO:0043433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the activity of a transcription factor, any factor involved in the initiation or regulation of transcription.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of molecular function","termid":"GO:0044092"},{"relation_name":"is_a","term_name":"regulation of DNA-binding transcription factor activity","termid":"GO:0051090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006355","GO:0006351","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of DNA-binding transcription factor activity","secondary_identifiers":["GO:2000824","GO:1904168"],"synonyms":[{"name":"down regulation of transcription factor activity","type":"exact"},{"name":"down-regulation of transcription factor activity","type":"exact"},{"name":"downregulation of transcription factor activity","type":"exact"},{"name":"inhibition of transcription factor activity","type":"narrow"},{"name":"negative regulation of DNA binding transcription factor activity","type":"exact"},{"name":"negative regulation of androgen receptor activity","type":"narrow"},{"name":"negative regulation of sequence-specific DNA binding transcription factor activity","type":"exact"},{"name":"negative regulation of thyroid hormone receptor activity","type":"narrow"},{"name":"negative regulation of transcription factor activity","type":"broad"}],"termid":"GO:0043433"}


id: PBO:0049297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase mu 1","termid":"PBO:0049297"}


id: FYPO:0000600
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 vacuolar transport begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vacuolar transport during vegetative growth","termid":"FYPO:0000597"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"delayed onset of vacuolar transport","synonyms":[{"name":"delayed onset of vacuolar protein transport","type":"narrow"},{"name":"delayed onset of vacuolar transport during mitotic cell cycle","type":"related"},{"name":"delayed onset of vacuolar transport during vegetative growth","type":"exact"},{"name":"delayed vacuolar transport","type":"exact"},{"name":"vacuolar transport: delayed","type":"related"}],"termid":"FYPO:0000600"}


id: GO:0150050
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the septin cytoskeleton contained within the postsynapse.","definition_xrefs":["PMID:28065648","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septin cytoskeleton","termid":"GO:0032156"},{"relation_name":"is_a","term_name":"postsynaptic cytoskeleton","termid":"GO:0099571"}],"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":"postsynaptic septin cytoskeleton","termid":"GO:0150050"}


id: GO:0110040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the nematode pharynx are generated and organized.","definition_xrefs":["PMID:20805556","GOC:rz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"}],"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":"nematode pharynx morphogenesis","termid":"GO:0110040"}


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


id: PBO:0083894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FG-nucleoporin component of central core of the nuclear pore complex; contributes directly to nucleocytoplasmic transport and maintenance of the nuclear pore complex (NPC) permeability barrier and is involved in gene tethering at the nuclear periphery; relocalizes to the cytosol in response to hypoxia; both NUP1 and NUP60 are homologous to human NUP153","termid":"PBO:0083894"}


id: GO:0030292
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Stops, prevents or reduces the activity of a protein tyrosine kinase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase inhibitor activity","termid":"GO:0004860"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0004857","GO:0030234","GO:0098772","GO:0140678"],"is_obsolete":false,"name":"protein tyrosine kinase inhibitor activity","termid":"GO:0030292"}


id: GO:1904637
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an ionomycin stimulus.","definition_xrefs":["GOC:TermGenie","PMID:17516843","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to ether","termid":"GO:0071362"},{"relation_name":"is_a","term_name":"cellular response to fatty acid","termid":"GO:0071398"},{"relation_name":"is_a","term_name":"response to ionomycin","termid":"GO:1904636"}],"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 ionomycin","termid":"GO:1904637"}


id: PBO:0086689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; includes a potential transmembrane domain; deletion results in slightly lengthened telomeres; SWAT-GFP and mCherry fusion proteins localize to the endoplasmic reticulum and vacuole respectively","termid":"PBO:0086689"}


id: MONDO:0000186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spondyloepimetaphyseal dysplasia with joint laxity (obsolete MONDO:0000186)","termid":"MONDO:0000186","xrefs":{"Monarch":{"xref_id":"0000186"}}}


id: PR:Q9HGQ0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC212.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HGQ0"],"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 C212.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC212.02","synonyms":[{"name":"Spom972h-SPAC212.02","type":"exact"}],"termid":"PR:Q9HGQ0"}


id: MONDO:0006745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm that affects the uterine corpus, and rarely, the ovaries, cervix, and vagina. In the uterine corpus it is classified as low grade or high grade endometrial stromal sarcoma. In the remainder of the anatomic sites it is classified as low grade endometrioid stromal sarcoma.","definition_xrefs":["NCIT:C8973"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare cancer of corpus uteri (obsolete MONDO:0016253)","termid":"MONDO:0016253"},{"relation_name":"is_a","term_name":"endometrial stromal tumor","termid":"MONDO:0003311"},{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"},{"relation_name":"is_a","term_name":"endometrial cancer","termid":"MONDO:0011962"}],"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":"endometrioid stromal sarcoma","secondary_identifiers":["MEDGEN:60196","MedDRA:10057649","ICDO:8930/3","MESH:D018203","Orphanet:213711","SCTID:699356008","ONCOTREE:ESS","DOID:4226","UMLS:C0206630","MedDRA:10048397","NORD:1086","GARD:6339","EFO:1000919"],"synonyms":[{"name":"ESS","type":"exact"},{"name":"Empty Sella Syndrome","type":"exact"},{"name":"endometrial stromal sarcoma","type":"exact"},{"name":"endometrial stromal sarcoma, high grade","type":"exact"},{"name":"endometrial stromal sarcomas","type":"exact"},{"name":"endometrioid stromal sarcoma","type":"exact"},{"name":"ess","type":"exact"},{"name":"sarcomas, endometrial stromal","type":"exact"},{"name":"stromal sarcoma of the corpus uteri","type":"exact"},{"name":"stromal sarcoma, endometrial","type":"exact"},{"name":"stromal sarcoma, endometrial, malignant","type":"exact"},{"name":"stromal sarcomas, endometrial","type":"exact"},{"name":"undifferentiated endometrial sarcoma","type":"exact"}],"termid":"MONDO:0006745","xrefs":{"Monarch":{"xref_id":"0006745"}}}


id: PATO:0000960
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000960 absolute opacity (obsolete PATO:0000960)","termid":"PATO:0000960"}


id: PBO:0036274
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Coiled-coil domain Telomerase Regulatory protein","termid":"PBO:0036274"}


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: PBO:0004204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione peroxidase Gpx1","termid":"PBO:0004204"}


id: GO:2000898
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glucomannan catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polysaccharide metabolic process","termid":"GO:0032881"},{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"regulates","term_name":"glucomannan catabolic process","termid":"GO:2000884"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of glucomannan catabolic process","synonyms":[{"name":"regulation of glucomannan catabolism","type":"exact"}],"termid":"GO:2000898"}


id: GO:0035358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the peroxisome proliferator activated receptor signaling pathway.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"peroxisome proliferator activated receptor signaling pathway","termid":"GO:0035357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of peroxisome proliferator activated receptor signaling pathway","synonyms":[{"name":"regulation of PPAR signaling pathway","type":"exact"},{"name":"regulation of peroxisome proliferator activated receptor signalling pathway","type":"exact"},{"name":"regulation of peroxisome proliferator-activated receptor signaling pathway","type":"exact"}],"termid":"GO:0035358"}


id: GO:0070596
data:
  {"annotated_genes":["SJAG_04184","SJAG_03057","SJAG_00610","SJAG_00424","SJAG_01028","SJAG_02916","SJAG_02278","SJAG_04666","SJAG_04236"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80554,72388,75115,75287,73175],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070600"},{"annotations":[104782,96839,94308,91309],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0070610"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (1->3)-alpha-D-glucans, compounds composed of glucose residues linked by (1->3)-alpha-D-glucosidic bonds.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-glucan biosynthetic process","termid":"GO:0030979"},{"relation_name":"is_a","term_name":"(1->3)-alpha-glucan metabolic process","termid":"GO:0070595"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00424":null,"SJAG_00610":null,"SJAG_01028":null,"SJAG_02278":null,"SJAG_02916":null,"SJAG_03057":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04666":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"(1->3)-alpha-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"1,3-alpha-glucan anabolism","type":"exact"},{"name":"1,3-alpha-glucan biosynthesis","type":"exact"},{"name":"1,3-alpha-glucan biosynthetic process","type":"exact"},{"name":"1,3-alpha-glucan formation","type":"exact"},{"name":"1,3-alpha-glucan synthesis","type":"exact"},{"name":"alpha-1,3 glucan anabolism","type":"exact"},{"name":"alpha-1,3 glucan biosynthesis","type":"exact"},{"name":"alpha-1,3 glucan biosynthetic process","type":"exact"},{"name":"alpha-1,3 glucan formation","type":"exact"},{"name":"alpha-1,3 glucan synthesis","type":"exact"}],"termid":"GO:0070596","terms_by_termid":{"GO:0070600":null,"GO:0070610":null}}


id: PBO:0042656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule 5","termid":"PBO:0042656"}


id: PR:O74549
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A NEDD8-conjugating enzyme Ubc12 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR24067:SF17","OMA:SCHPO04749"],"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":"NEDD8-conjugating enzyme ubc12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC777.10c","secondary_identifiers":["UniProtKB:O74549"],"synonyms":[{"name":"RUB1-conjugating enzyme (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RUB1-protein ligase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-UBE2M","type":"exact"},{"name":"ubiquitin carrier protein 12 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74549"}


id: PBO:0070694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L8 pseudogene 3","termid":"PBO:0070694"}


id: PBO:0002316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk18 (predicted)","termid":"PBO:0002316"}


id: MONDO:0850346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rhabdomyosarcoma located in the oral cavity.","definition_xrefs":["DOID:0080900"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhabdomyosarcoma","termid":"MONDO:0005212"},{"relation_name":"is_a","term_name":"oral cavity cancer","termid":"MONDO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"oral rhabdomyosarcoma","termid":"MONDO:0850346","xrefs":{"Monarch":{"xref_id":"0850346"}}}


id: FYPO:0001720
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a specific transport process is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport phenotype","termid":"FYPO:0000149"},{"relation_name":"is_a","term_name":"abnormal cellular process","termid":"FYPO:0000628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abnormal transport","termid":"FYPO:0001720"}


id: PR:P87146
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitochondrial import inner membrane translocase subunit Tim22 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR14110:SF0","OMA:SCHPO03639","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":"mitochondrial import inner membrane translocase subunit tim22 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC25H2.04c","secondary_identifiers":["UniProtKB:P87146"],"synonyms":[{"name":"Spom972h-TIMM22","type":"exact"}],"termid":"PR:P87146"}


id: PBO:0067753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 52","termid":"PBO:0067753"}


id: SO:0000594
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Members of the box H/ACA family contain an ACA triplet, exactly 3 nt upstream from the 3' end and an H-box in a hinge region that links two structurally similar functional domains of the molecule. Both boxes are important for snoRNA biosynthesis and function. A few box H/ACA snoRNAs are involved in rRNA processing; most others are known or predicted to participate in selection of uridine nucleosides in rRNA to be converted to pseudouridines. Site selection is mediated by direct base pairing of the snoRNA with rRNA through one or both targeting domains.","direct_ancestors":[{"relation_name":"derives_from","term_name":"H_ACA_box_snoRNA_primary_transcript","termid":"SO:0000596"},{"relation_name":"is_a","term_name":"snoRNA","termid":"SO:0000275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H_ACA_box_snoRNA","synonyms":[{"name":"H ACA box snoRNA","type":"exact"},{"name":"H/ACA box snoRNA","type":"exact"},{"name":"SNORA","type":"exact"},{"name":"box H/ACA snoRNA","type":"exact"}],"termid":"SO:0000594"}


id: PBO:0052948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratinocyte differentiation associated protein","termid":"PBO:0052948"}


id: MONDO:0007485
data:
  {"annotated_genes":["SJAG_05979"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87730],"is_not":false,"summary":null,"term":"MONDO:0007485"}]},"cv_name":"mondo","definition":"A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERC on chromosome 3q26.2.","definition_xrefs":["DOID:0070014"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dyskeratosis congenita","termid":"MONDO:0015780"},{"relation_name":"is_a","term_name":"telomere syndrome","termid":"MONDO:0100137"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019303"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0019303","MONDO:0005093"],"is_obsolete":false,"name":"dyskeratosis congenita, autosomal dominant 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C565079","UMLS:C4551974","OMIM:127550","SCTID:707273001","GARD:6299","MEDGEN:1645250","NCIT:C176921"],"synonyms":[{"name":"DKCA","type":"related"},{"name":"DKCA1","type":"exact"},{"name":"autosomal dominant dyskeratosis congenita","type":"related"},{"name":"autosomal dominant dyskeratosis congenita 1","type":"related"},{"name":"dyskeratosis congenita Scoggins type","type":"related"},{"name":"dyskeratosis congenita autosomal dominant","type":"related"},{"name":"dyskeratosis congenita, Scoggins type","type":"exact"},{"name":"dyskeratosis congenita, autosomal dominant 1","type":"exact"},{"name":"dyskeratosis congenita, autosomal dominant type 1","type":"exact"}],"termid":"MONDO:0007485","terms_by_termid":{"MONDO:0007485":null},"xrefs":{"Monarch":{"xref_id":"0007485"}}}


id: PBO:0002932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sec7 domain protein, ARF GEF (predicted)","termid":"PBO:0002932"}


id: PBO:0079278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TELO2 interacting protein 2","termid":"PBO:0079278"}


id: PR:000037083
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein complex composed of two subunits of Schizosaccharomyces pombe tropomyosin cdc8.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tropomyosin cdc8","termid":"PR:000028197"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomyosin cdc8 homodimer (Schizosaccharomyces pombe)","pombase_gene_id":"SPAC27F1.02c","synonyms":[{"name":"Spom-(cdc8)*2","type":"exact"}],"termid":"PR:000037083"}


id: PBO:0116541
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in vertebrsates","termid":"PBO:0116541"}


id: GO:2001043
data:
  {"annotated_genes":["SJAG_01774","SJAG_02645"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91603,109916],"is_not":false,"summary":null,"term":"GO:2001043"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the process of physically separating the septal cell wall material by enzymatic digestion, that occurs after daughter cells are separated by cytokinesis.","definition_xrefs":["GOC:obol","GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of septum digestion after cytokinesis","termid":"GO:0010590"},{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"positively_regulates","term_name":"septum digestion after cytokinesis","termid":"GO:0000920"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01774":null,"SJAG_02645":null},"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 septum digestion after cytokinesis","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"positive regulation of cell separation after cytokinesis","type":"related"},{"name":"positive regulation of cytokinetic cell separation","type":"related"}],"termid":"GO:2001043","terms_by_termid":{"GO:2001043":null}}


id: GO:0045860
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein kinase activity.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein phosphorylation","termid":"GO:0001934"},{"relation_name":"is_a","term_name":"positive regulation of kinase activity","termid":"GO:0033674"},{"relation_name":"is_a","term_name":"regulation of protein kinase activity","termid":"GO:0045859"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein kinase activity","synonyms":[{"name":"stimulation of protein kinase activity","type":"narrow"},{"name":"up regulation of protein kinase activity","type":"exact"},{"name":"up-regulation of protein kinase activity","type":"exact"},{"name":"upregulation of protein kinase activity","type":"exact"}],"termid":"GO:0045860"}


id: PBO:0041506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 14 open reading frame 28","termid":"PBO:0041506"}


id: GO:0043445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of acetone, propan-2-one.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete acetone biosynthetic process (obsolete GO:0043445)","synonyms":[{"name":"2-propanone biosynthesis","type":"exact"},{"name":"2-propanone biosynthetic process","type":"exact"},{"name":"acetone anabolism","type":"exact"},{"name":"acetone biosynthesis","type":"exact"},{"name":"acetone formation","type":"exact"},{"name":"acetone synthesis","type":"exact"},{"name":"dimethyl ketone biosynthesis","type":"exact"},{"name":"dimethyl ketone biosynthetic process","type":"exact"},{"name":"propan-2-one biosynthesis","type":"exact"},{"name":"propan-2-one biosynthetic process","type":"exact"}],"termid":"GO:0043445"}


id: PBO:0086545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved among S. cerevisiae strains; YDR102C is not an essential gene; homozygous diploid deletion strain exhibits high budding index","termid":"PBO:0086545"}


id: PBO:0049602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 5","termid":"PBO:0049602"}


id: PBO:0046922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 41 member A, Y-linked 1","termid":"PBO:0046922"}


id: GO:0030070
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of mature insulin by proteolysis of the precursor preproinsulin. The signal sequence is first cleaved from preproinsulin to form proinsulin; proinsulin is then cleaved to release the C peptide, leaving the A and B chains of mature insulin linked by disulfide bridges.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide hormone processing","termid":"GO:0016486"},{"relation_name":"is_a","term_name":"insulin metabolic process","termid":"GO:1901142"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0051604","GO:0008150"],"is_obsolete":false,"name":"insulin processing","secondary_identifiers":["Reactome:R-HSA-264876"],"termid":"GO:0030070"}


id: PR:G2TRK9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- new13 gene.","definition_xrefs":["UniProtKB:G2TRK9","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 new13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.14","synonyms":[{"name":"Spom972h-new13","type":"exact"}],"termid":"PR:G2TRK9"}


id: GO:0072354
data:
  {"annotated_genes":["SJAG_00678"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[80020],"is_not":false,"summary":null,"term":"GO:0072354"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H3-threonine (position 3) + ATP = histone H3-phosphothreonine (position 3) + ADP. This reaction is the addition of a phosphate group to the threonine residue at position 3 of histone H3.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"},{"relation_name":"is_a","term_name":"histone H3 kinase activity","termid":"GO:0140996"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00678":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016301","GO:0140096","GO:0003824","GO:0003674","GO:0016740","GO:0004672"],"is_obsolete":false,"name":"histone H3T3 kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"histone H3-T3 kinase activity","type":"exact"},{"name":"histone kinase activity (H3-T3 specific)","type":"exact"},{"name":"histone threonine kinase activity (H3-T3 specific)","type":"exact"},{"name":"histone-threonine kinase activity (H3-T3 specific)","type":"exact"}],"termid":"GO:0072354","terms_by_termid":{"GO:0072354":null}}


id: PBO:0040211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASXL3 divergent transcript","termid":"PBO:0040211"}


id: GO:0071960
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the association between sister chromatids of a replicated chromosome along the length of the centromeric region is maintained as chromosomes condense, attach to the spindle in a bipolar orientation, and congress to the metaphase plate during a mitotic cell cycle.","definition_xrefs":["PMID:1708436","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of mitotic sister chromatid cohesion","termid":"GO:0034088"},{"relation_name":"part_of","term_name":"mitotic sister chromatid cohesion, centromeric","termid":"GO:0071962"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"maintenance of mitotic sister chromatid cohesion, centromeric","synonyms":[{"name":"maintenance of centromeric mitotic sister chromatin cohesion","type":"exact"},{"name":"maintenance of mitotic sister chromatin cohesion at centromere","type":"exact"},{"name":"maintenance of sister chromatin cohesion at centromere at mitosis","type":"exact"}],"termid":"GO:0071960"}


id: PBO:0016096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MBF complex corepressor Nrm1","termid":"PBO:0016096"}


id: GO:0004258
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the release of a C-terminal amino acid with a broad specificity.","definition_xrefs":["EC:3.4.16.5"],"gene_count":0,"genotype_count":0,"name":"obsolete vacuolar carboxypeptidase Y (obsolete GO:0004258)","synonyms":[{"name":"vacuolar carboxypeptidase Y","type":"exact"}],"termid":"GO:0004258"}


id: MONDO:0014139
data:
  {"annotated_genes":["SJAG_00183"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87860],"is_not":false,"summary":null,"term":"MONDO:0014139"}]},"cv_name":"mondo","definition":"Any Ehlers-Danlos syndrome, spondylodysplastic type in which the cause of the disease is a mutation in the B3GALT6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome, spondylodysplastic type","termid":"MONDO:0007526"},{"relation_name":"is_a","term_name":"B3GALT6-congenital disorder of glycosylation","termid":"MONDO:0100586"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00183":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"Ehlers-Danlos syndrome, spondylodysplastic type, 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:815540","GARD:15947","Orphanet:536467","OMIM:615349","UMLS:C3809210"],"synonyms":[{"name":"B3GALT6 Ehlers-Danlos syndrome progeroid type","type":"exact"},{"name":"B3GALT6-related spEDS","type":"exact"},{"name":"B3GALT6-related spondylodysplastic EDS","type":"exact"},{"name":"Beta3GalT6-deficient EDS","type":"exact"},{"name":"EDSP2","type":"exact"},{"name":"EDSSPD2","type":"exact"},{"name":"Ehlers-Danlos syndrome progeroid type 2","type":"exact"},{"name":"Ehlers-Danlos syndrome progeroid type caused by mutation in B3GALT6","type":"exact"},{"name":"Ehlers-Danlos syndrome, progeroid type, 2","type":"exact"},{"name":"Ehlers-Danlos syndrome, progeroid type, 2, formerly","type":"related"},{"name":"Ehlers-Danlos syndrome, spondylodysplastic type, 2","type":"exact"},{"name":"spEDS-B3GALT6","type":"exact"}],"termid":"MONDO:0014139","terms_by_termid":{"MONDO:0014139":null},"xrefs":{"Monarch":{"xref_id":"0014139"}}}


id: FYPO:0004127
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the dimethylation of lysine at position 4 of histone H3 at protein-coding genes occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K4 methylation during vegetative growth","termid":"FYPO:0002330"},{"relation_name":"is_a","term_name":"decreased histone H3-K4 dimethylation during vegetative growth","termid":"FYPO:0002367"}],"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"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0002274","FYPO:0002494"],"is_obsolete":false,"name":"decreased histone H3-K4 dimethylation at protein coding gene during vegetative growth","synonyms":[{"name":"decreased histone H3 K4 dimethylation at protein coding gene during vegetative growth","type":"exact"},{"name":"decreased histone H3-K4 dimethylation at protein coding gene during mitotic cell cycle","type":"related"},{"name":"decreased histone H3K4 dimethylation at protein coding gene during vegetative growth","type":"exact"},{"name":"decreased histone H3K4me2 at protein coding gene during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K4 dimethylation at protein coding gene during vegetative growth","type":"exact"},{"name":"reduced histone H3-K4 dimethylation at protein coding gene during vegetative growth","type":"exact"}],"termid":"FYPO:0004127"}


id: FYPO:0006015
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell has more than one septum, and forms a mating projection.","definition_xrefs":["PomBase:mah","PMID:28410370"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiseptate cell","termid":"FYPO:0004295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"multiseptate cell with shmoo","synonyms":[{"name":"large non-mated cells","type":"related"},{"name":"multiseptate shmooing cell","type":"exact"}],"termid":"FYPO:0006015"}


id: GO:0033945
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of cellobiose from the reducing end of xyloglucans consisting of a beta-(1->4) linked glucan carrying alpha-D-xylosyl groups on O-6 of the glucose residues. To be a substrate, the first residue must be unsubstituted, the second residue may bear a xylosyl group, whether further glycosylated or not, and the third residue, which becomes the new terminus by the action of the enzyme, is preferably xylosylated, but this xylose residue must not be further substituted.","definition_xrefs":["EC:3.2.1.150"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824","GO:0016798"],"is_obsolete":false,"name":"oligoxyloglucan reducing-end-specific cellobiohydrolase activity","secondary_identifiers":["MetaCyc:3.2.1.150-RXN"],"synonyms":[{"name":"oligoxyloglucan reducing end-specific cellobiohydrolase activity","type":"related"},{"name":"oligoxyloglucan reducing-end cellobiohydrolase activity","type":"related"}],"termid":"GO:0033945"}


id: PBO:0053492
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 470","termid":"PBO:0053492"}


id: PBO:0049889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERC2 pseudogene 8","termid":"PBO:0049889"}


id: PBO:0077451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM183A pseudogene 1","termid":"PBO:0077451"}


id: MONDO:0971050
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated optic neuritis","termid":"MONDO:0044688"}],"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":"relapsing isolated optic neuritis","secondary_identifiers":["Orphanet:659634","UMLS:C5925139","MEDGEN:1863611"],"termid":"MONDO:0971050","xrefs":{"Monarch":{"xref_id":"0971050"}}}


id: GO:0007147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which the second meiotic division occurs in the female germline.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiosis II","termid":"GO:0007135"},{"relation_name":"is_a","term_name":"female meiotic nuclear division","termid":"GO:0007143"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0140013"],"is_obsolete":false,"name":"female meiosis II","synonyms":[{"name":"female meiosis II nuclear division","type":"exact"}],"termid":"GO:0007147"}


id: PBO:0069313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 571, pseudogene","termid":"PBO:0069313"}


id: PBO:0067588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 749, pseudogene","termid":"PBO:0067588"}


id: PBO:0089976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snoRNP assembly factor Naf1","termid":"PBO:0089976"}


id: PBO:0084155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-affinity S-methylmethionine permease; required for utilization of S-methylmethionine as a sulfur source; has similarity to S-adenosylmethionine permease Sam3p","termid":"PBO:0084155"}


id: PBO:0073646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sigma non-opioid intracellular receptor 1","termid":"PBO:0073646"}


id: PATO:0002228
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A tapered shape quality inhering in a bearer by virtue of the bearer's tapering gradually to a sharp point.","direct_ancestors":[{"relation_name":"is_a","term_name":"tapered","termid":"PATO:0001500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acuminate","termid":"PATO:0002228"}


id: PBO:0017458
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-hyperparasitized_by","termid":"PBO:0017458"}


id: PBO:0047762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folate receptor 3 pseudogene 1","termid":"PBO:0047762"}


id: GO:1905639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mitochondrial mRNA catabolic process.","definition_xrefs":["PMID:27122350","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mitochondrial RNA catabolic process","termid":"GO:0000962"},{"relation_name":"is_a","term_name":"positive regulation of mRNA catabolic process","termid":"GO:0061014"},{"relation_name":"is_a","term_name":"regulation of mitochondrial mRNA catabolic process","termid":"GO:1905637"},{"relation_name":"positively_regulates","term_name":"mitochondrial mRNA catabolic process","termid":"GO:0000958"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0016071"],"is_obsolete":false,"name":"positive regulation of mitochondrial mRNA catabolic process","synonyms":[{"name":"activation of mitochondrial mRNA catabolic process","type":"narrow"},{"name":"up regulation of mitochondrial mRNA catabolic process","type":"exact"},{"name":"up-regulation of mitochondrial mRNA catabolic process","type":"exact"},{"name":"upregulation of mitochondrial mRNA catabolic process","type":"exact"}],"termid":"GO:1905639"}


id: PBO:0040368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase peripheral stalk-membrane subunit b pseudogene 5","termid":"PBO:0040368"}


id: GO:0044196
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small, dense body one or more of which are present in the nucleus of eukaryotic host cells.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell nuclear part","termid":"GO:0044094"}],"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 nucleolus","termid":"GO:0044196"}


id: GO:0034177
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of toll-like receptor 12 signaling pathway.","definition_xrefs":["GOC:add","PMID:16551253","PMID:17328678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of toll-like receptor 12 signaling pathway","termid":"GO:0034175"},{"relation_name":"is_a","term_name":"positive regulation of pattern recognition receptor signaling pathway","termid":"GO:0062208"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"toll-like receptor 12 signaling pathway","termid":"GO:0034174"}],"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:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of toll-like receptor 12 signaling pathway","synonyms":[{"name":"positive regulation of TLR12 signaling pathway","type":"exact"},{"name":"positive regulation of toll-like receptor 12 signalling pathway","type":"exact"}],"termid":"GO:0034177"}


id: PBO:0091274
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"I:g.682994delC","termid":"PBO:0091274"}


id: GO:0008035
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to high-density lipoprotein particle, a lipoprotein particle with a high density (typically 1.063-1.21 g/ml) and a diameter of 5-10 nm that contains APOAs and may contain APOCs and APOE.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle binding","termid":"GO:0071813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"high-density lipoprotein particle binding","synonyms":[{"name":"HDL binding","type":"exact"}],"termid":"GO:0008035"}


id: GO:1900558
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving austinol.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"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":"austinol metabolic process","synonyms":[{"name":"austinol metabolism","type":"exact"}],"termid":"GO:1900558"}


id: MONDO:0007326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete paroxysmal nonkinesigenic dyskinesia 1 (obsolete MONDO:0007326)","secondary_identifiers":["NANDO:1200519"],"termid":"MONDO:0007326","xrefs":{"Monarch":{"xref_id":"0007326"}}}


id: PR:O74926
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rbd2 gene.","definition_xrefs":["UniProtKB:O74926","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":"rhomboid protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC790.03","synonyms":[{"name":"Spom972h-rbd2","type":"exact"}],"termid":"PR:O74926"}


id: PBO:0109396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 23B","termid":"PBO:0109396"}


id: PBO:0083398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps ORF TPD3/YAL016W","termid":"PBO:0083398"}


id: PBO:0028103
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_galactose_carbon_source","termid":"PBO:0028103"}


id: PBO:0081677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 598, E3 ubiquitin ligase","termid":"PBO:0081677"}


id: GO:0051915
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a chemical substance activates synaptic plasticity, the ability of synapses to change as circumstances require.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of synaptic plasticity by chemical substance","termid":"GO:0051914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"induction of synaptic plasticity by chemical substance","synonyms":[{"name":"activation of synaptic plasticity by chemical substance","type":"exact"},{"name":"activation of synaptic plasticity by drug","type":"narrow"},{"name":"induction of synaptic plasticity by drug","type":"narrow"}],"termid":"GO:0051915"}


id: PBO:0086460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative metalloprotease; overproduction suppresses lethality due to expression of the dominant PET9 allele AAC2-A128P","termid":"PBO:0086460"}


id: GO:0071978
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Bacterial-type flagellum-dependent cell motility in which the action of numerous flagella results in the smooth movement of a group of cells along a solid surface. Swarming motility is observed in groups of bacteria.","definition_xrefs":["PMID:14527279","GOC:cilia","PMID:18461074"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial-type flagellum-dependent cell motility","termid":"GO:0071973"}],"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":"bacterial-type flagellum-dependent swarming motility","synonyms":[{"name":"bacterial-type flagellar swarming motility","type":"related"},{"name":"bacterial-type flagellum-mediated cell swarming","type":"exact"}],"termid":"GO:0071978"}


id: MONDO:0100152
data:
  {"annotated_genes":["SJAG_04754"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010584"}]},"cv_name":"mondo","definition":"Any dyskeratosis congenita in which the cause of the disease is a mutation in the DKC1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene","PMID:12437656","PMID:14648217","PMID:10583221","PMID:19633571"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dyskeratosis congenita","termid":"MONDO:0015780"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04754":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"DKC1-related disorder","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"DKC1-related disorder","type":"exact"}],"termid":"MONDO:0100152","terms_by_termid":{"MONDO:0010584":null},"xrefs":{"Monarch":{"xref_id":"0100152"}}}


id: PBO:0067689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5.8S ribosomal N1","termid":"PBO:0067689"}


id: PBO:0067767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 67","termid":"PBO:0067767"}


id: PBO:0060249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYCL proto-oncogene, bHLH transcription factor","termid":"PBO:0060249"}


id: GO:0048330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of axial mesoderm cell fate specification.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of axial mesodermal cell fate specification","termid":"GO:0048328"},{"relation_name":"is_a","term_name":"positive regulation of mesodermal cell fate specification","termid":"GO:0048337"},{"relation_name":"positively_regulates","term_name":"axial mesodermal cell fate specification","termid":"GO:0048327"}],"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 axial mesodermal cell fate specification","synonyms":[{"name":"activation of axial mesodermal cell fate specification","type":"narrow"},{"name":"stimulation of axial mesodermal cell fate specification","type":"narrow"},{"name":"up regulation of axial mesodermal cell fate specification","type":"exact"},{"name":"up-regulation of axial mesodermal cell fate specification","type":"exact"},{"name":"upregulation of axial mesodermal cell fate specification","type":"exact"}],"termid":"GO:0048330"}


id: PBO:0049185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"grainyhead like transcription factor 2","termid":"PBO:0049185"}


id: GO:0048087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of the developmental process that results in the deposition of coloring matter in an organism.","definition_xrefs":["GOC:jid","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental pigmentation","termid":"GO:0048070"},{"relation_name":"is_a","term_name":"positive regulation of biological process","termid":"GO:0048518"},{"relation_name":"positively_regulates","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":"positive regulation of developmental pigmentation","synonyms":[{"name":"activation of developmental pigmentation","type":"narrow"},{"name":"stimulation of developmental pigmentation","type":"narrow"},{"name":"up regulation of developmental pigmentation","type":"exact"},{"name":"up-regulation of developmental pigmentation","type":"exact"},{"name":"upregulation of developmental pigmentation","type":"exact"}],"termid":"GO:0048087"}


id: PBO:0040819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BH3 interacting domain death agonist","termid":"PBO:0040819"}


id: GO:0090304
data:
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id: GO:0051784
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id: GO:0030513
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id: PBO:0055950
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id: MONDO:0003302
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id: MONDO:0014703
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id: GO:0102966
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id: PBO:0046691
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id: GO:0010194
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id: PBO:0063392
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id: PBO:0073553
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id: MONDO:0014824
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id: PBO:0059610
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id: GO:0097292
data:
  {"annotated_genes":["SJAG_01298","SJAG_06634"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77412,110238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving XMP, xanthosine monophosphate.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"purine ribonucleoside monophosphate metabolic process","termid":"GO:0009167"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01298":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"XMP metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"XMP metabolism","type":"exact"}],"termid":"GO:0097292","terms_by_termid":{"GO:0032265":null}}


id: PBO:0065574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostaglandin-endoperoxide synthase 2","termid":"PBO:0065574"}


id: GO:0010485
data:
  {"annotated_genes":["SJAG_00676","SJAG_03537","SJAG_02990"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75794,100883],"is_not":false,"summary":null,"term":"GO:0010485"},{"annotations":[90291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043997"},{"annotations":[90292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043995"},{"annotations":[90293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043996"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H4 = CoA + acetyl-histone H4.","definition_xrefs":["PMID:19056256"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone acetyltransferase activity","termid":"GO:0004402"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00676":null,"SJAG_02990":null,"SJAG_03537":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0034212","GO:0003674","GO:0016740","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"histone H4 acetyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"H4 histone acetylase activity","type":"exact"},{"name":"H4 histone acetyltransferase activity","type":"exact"}],"termid":"GO:0010485","terms_by_termid":{"GO:0010485":null,"GO:0043995":null,"GO:0043996":null,"GO:0043997":null}}


id: GO:1900767
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving fonsecin.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol metabolic process","termid":"GO:0006066"},{"relation_name":"is_a","term_name":"ether metabolic process","termid":"GO:0018904"},{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"polyketide metabolic process","termid":"GO:0030638"},{"relation_name":"is_a","term_name":"naphtho-gamma-pyrone metabolic process","termid":"GO:1900785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"fonsecin metabolic process","synonyms":[{"name":"fonsecin metabolism","type":"exact"}],"termid":"GO:1900767"}


id: PBO:0051202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 4-30-1","termid":"PBO:0051202"}


id: GO:1990330
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterotetrameric protein complex involved in the sulfur transfer during iron-sulfur cluster assembly and in the modification of tRNA wobble positions. In E. coli it consists of a central IscS dimer with the IscU protomers attached to one of the IscS units each via a disulfide (-SSH) group.","definition_xrefs":["GOC:bhm","PMID:20404999"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-cysteine desulfurase complex","termid":"GO:1990221"},{"relation_name":"is_a","term_name":"iron-sulfur cluster assembly complex","termid":"GO:1990229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005829","GO:0032991"],"is_obsolete":false,"name":"IscS-IscU complex","termid":"GO:1990330"}


id: PBO:0081774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 705B","termid":"PBO:0081774"}


id: GO:0075269
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of aecium development, a process in which a cuplike structure containing chains of aeciospores is formed.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of spore-bearing organ development","termid":"GO:0075261"},{"relation_name":"is_a","term_name":"regulation of aecium development","termid":"GO:0075268"},{"relation_name":"positively_regulates","term_name":"aecium development","termid":"GO:0075267"}],"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 aecium development","termid":"GO:0075269"}


id: GO:1901945
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of miltiradiene.","definition_xrefs":["GOC:TermGenie","PMID:22027823"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpene catabolic process","termid":"GO:0046247"},{"relation_name":"is_a","term_name":"miltiradiene metabolic process","termid":"GO:1901944"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"miltiradiene catabolic process","synonyms":[{"name":"miltiradiene breakdown","type":"exact"},{"name":"miltiradiene catabolism","type":"exact"},{"name":"miltiradiene degradation","type":"exact"}],"termid":"GO:1901945"}


id: MONDO:0011910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal dominant limb-girdle muscular dystrophy type 1C (obsolete MONDO:0011910)","secondary_identifiers":["SCTID:719986000","MESH:C563362","OMIM:607801","Orphanet:265","DOID:0110302","NCIT:C148318"],"termid":"MONDO:0011910","xrefs":{"Monarch":{"xref_id":"0011910"}}}


id: PBO:0047480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"farnesyl diphosphate synthase pseudogene 7","termid":"PBO:0047480"}


id: FYPO:0007016
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at the 3' ends of rRNA genes in ribosomal DNA repeat regions is increased.","definition_xrefs":["PomBase:mah","PMID:31294478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to chromatin at rDNA","termid":"FYPO:0004032"},{"relation_name":"is_a","term_name":"abnormal protein localization to chromatin at 3' end of genes","termid":"FYPO:0007733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased protein localization to chromatin at 3' end of rRNA genes","synonyms":[{"name":"increased protein localisation to chromatin at 3' end of rRNA genes","type":"exact"},{"name":"increased protein localization to chromatin at 3' end of rRNA genes during mitotic cell cycle","type":"related"},{"name":"increased protein localization to chromatin at 3' end of rRNA genes during vegetative growth","type":"exact"},{"name":"increased protein localization to chromatin at 3' end of ribosomal RNA genes","type":"exact"},{"name":"increased protein localization to chromatin at rRNA genes at 3' end","type":"exact"}],"termid":"FYPO:0007016"}


id: PBO:0002152
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by Cuf1","termid":"PBO:0002152"}


id: PBO:0042483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDH8 antisense RNA 1","termid":"PBO:0042483"}


id: GO:0019121
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of linking a protein to peptidoglycan via the epsilon amino group of lysine to the diaminopimelic acid of the peptidoglycan.","definition_xrefs":["RESID:AA0218"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidoglycan-protein cross-linking via N6-mureinyl-L-lysine (obsolete GO:0019121)","termid":"GO:0019121"}


id: SO:0000564
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one V-gene, one DJ-gene, one J-gene and one C-gene.","direct_ancestors":[{"relation_name":"has_part","term_name":"V_gene_segment","termid":"SO:0000466"},{"relation_name":"has_part","term_name":"J_gene_segment","termid":"SO:0000470"},{"relation_name":"has_part","term_name":"C_gene_segment","termid":"SO:0000478"},{"relation_name":"has_part","term_name":"DJ_gene_segment","termid":"SO:0000572"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_gene_cluster","termid":"SO:0000938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V_DJ_J_C_cluster","synonyms":[{"name":"V DJ J C cluster","type":"exact"},{"name":"V-(DJ)-J-C-CLUSTER","type":"exact"}],"termid":"SO:0000564"}


id: PR:O60184
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ssn6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60184"],"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":"general transcriptional corepressor ssn6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC23E6.09","synonyms":[{"name":"Spom972h-ssn6","type":"exact"}],"termid":"PR:O60184"}


id: GO:0061635
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that affects the structure and integrity of a protein complex by altering the likelihood of its assembly or disassembly.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"}],"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 protein complex stability","termid":"GO:0061635"}


id: PBO:0069579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 853, pseudogene","termid":"PBO:0069579"}


id: PBO:0061893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opsin 1, medium wave sensitive","termid":"PBO:0061893"}


id: GO:0002044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of endothelial cells into the extracellular matrix in order to form new blood vessels during intussusceptive angiogenesis.","definition_xrefs":["PMID:16391003"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel endothelial cell migration","termid":"GO:0043534"},{"relation_name":"part_of","term_name":"intussusceptive angiogenesis","termid":"GO:0002041"}],"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":"blood vessel endothelial cell migration involved in intussusceptive angiogenesis","termid":"GO:0002044"}


id: GO:0102214
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: coenzyme A + ATP + an omega-hydroxy fatty acid = diphosphoric acid + AMP + a omega-hydroxyacyl-CoA.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete omega-hydroxy fatty acyl-CoA synthetase activity (obsolete GO:0102214)","termid":"GO:0102214"}


id: GO:0004777
data:
  {"annotated_genes":["SJAG_00674","SJAG_03293"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77801,79325],"is_not":false,"summary":null,"term":"GO:0004777"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: succinate semialdehyde + NAD+ + H2O = succinate + NADH + H+.","definition_xrefs":["RHEA:13217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"succinate-semialdehyde dehydrogenase [NAD(P)+] activity","termid":"GO:0009013"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00674":null,"SJAG_03293":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:0003824","GO:0016491"],"is_obsolete":false,"name":"succinate-semialdehyde dehydrogenase (NAD+) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-888548","EC:1.2.1.24","GO:0008952","MetaCyc:SUCCINATE-SEMIALDEHYDE-DEHYDROGENASE-RXN"],"synonyms":[{"name":"succinate semialdehyde dehydrogenase activity","type":"broad"},{"name":"succinate semialdehyde:NAD+ oxidoreductase activity","type":"related"},{"name":"succinate-semialdehyde dehydrogenase activity","type":"broad"},{"name":"succinate-semialdehyde:NAD+ oxidoreductase activity","type":"related"},{"name":"succinic semialdehyde dehydrogenase activity","type":"broad"},{"name":"succinyl semialdehyde dehydrogenase activity","type":"related"}],"termid":"GO:0004777","terms_by_termid":{"GO:0004777":null}}


id: MONDO:0004317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple meningiomas that arises from the spinal meninges.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intraspinal meningioma","termid":"MONDO:0001279"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple spinal canal and spinal cord meningioma","secondary_identifiers":["NCIT:C5275","DOID:7646","MEDGEN:235341","UMLS:C1334825"],"synonyms":[{"name":"multiple Meningiomas of spinal canal and spinal cord","type":"exact"},{"name":"multiple intraspinal Meningiomas","type":"exact"},{"name":"multiple meningiomas of the spinal canal and spinal cord","type":"exact"},{"name":"multiple spinal canal and spinal cord Meningiomas","type":"exact"}],"termid":"MONDO:0004317","xrefs":{"Monarch":{"xref_id":"0004317"}}}


id: PATO:0000497
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000497 relative rhythym value (obsolete PATO:0000497)","termid":"PATO:0000497"}


id: GO:0071257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an electrical stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to electrical stimulus","termid":"GO:0051602"},{"relation_name":"is_a","term_name":"cellular response to abiotic stimulus","termid":"GO:0071214"}],"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 electrical stimulus","synonyms":[{"name":"cellular response to electricity","type":"related"}],"termid":"GO:0071257"}


id: FYPO:0006614
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 termination of transcription by RNA polymerase II occurs to a greater extent than normal. Termination of all transcripts, or a subset of transcripts, may be affected.","definition_xrefs":["PomBase:mah","GO:0006369"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription during vegetative growth","termid":"FYPO:0000780"},{"relation_name":"is_a","term_name":"abnormal termination of RNA polymerase II transcription","termid":"FYPO:0004811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000294","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"increased termination of RNA polymerase II transcription","synonyms":[{"name":"increased RNA polymerase II transcription termination","type":"exact"},{"name":"increased termination of RNA polymerase II transcription during mitotic cell cycle","type":"related"},{"name":"increased termination of RNA polymerase II transcription during vegetative growth","type":"exact"}],"termid":"FYPO:0006614"}


id: PBO:0073492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingosine-1-phosphate phosphatase 1","termid":"PBO:0073492"}


id: GO:0003790
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete actin modulating activity (obsolete GO:0003790)","synonyms":[{"name":"actin modulating activity","type":"exact"}],"termid":"GO:0003790"}


id: PBO:0088519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoskeletal protein binding protein Sla1 family, Shd1","termid":"PBO:0088519"}


id: PBO:0000605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G-patch domain","termid":"PBO:0000605"}


id: PR:O59697
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppk25 gene.","definition_xrefs":["UniProtKB:O59697","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 ppk25 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC32C12.03c","synonyms":[{"name":"Spom972h-ppk25","type":"exact"}],"termid":"PR:O59697"}


id: FYPO:0000812
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 vacuole organization is abnormal. Vacuole organization results in the assembly, arrangement of constituent parts, or disassembly of a vacuole.","definition_xrefs":["PomBase:mah","GO:0007033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular component organization during vegetative growth","termid":"FYPO:0001353"},{"relation_name":"is_a","term_name":"abnormal vacuole organization","termid":"FYPO:0002803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abnormal vacuole organization during vegetative growth","synonyms":[{"name":"abnormal vacuolar organisation during vegetative growth","type":"exact"},{"name":"abnormal vacuolar organization during vegetative growth","type":"exact"},{"name":"abnormal vacuole organisation during vegetative growth","type":"exact"},{"name":"abnormal vacuole organization during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000812"}


id: PBO:0116684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARF like GTPase 14 effector protein","termid":"PBO:0116684"}


id: MONDO:0014650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has material basis in heterozygous mutation in the GAL gene on chromosome 11q13.","definition_xrefs":["PMID:25691535","DOID:0060754"],"direct_ancestors":[{"relation_name":"is_a","term_name":"temporal lobe epilepsy","termid":"MONDO:0005115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"familial temporal lobe epilepsy 8","secondary_identifiers":["OMIM:616461","MEDGEN:909158","GARD:16116","UMLS:C4225318"],"synonyms":[{"name":"ETL8","type":"exact"},{"name":"epilepsy, familial temporal lobe, 8","type":"related"},{"name":"epilepsy, familial temporal lobe, type 8","type":"exact"},{"name":"familial temporal lobe epilepsy type 8","type":"exact"}],"termid":"MONDO:0014650","xrefs":{"Monarch":{"xref_id":"0014650"}}}


id: MONDO:0006304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma that arises from the minor salivary glands.","definition_xrefs":["NCIT:C5948"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"minor salivary gland carcinoma","termid":"MONDO:0045069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"minor salivary gland adenocarcinoma","secondary_identifiers":["UMLS:C1334768","EFO:1000379","MEDGEN:235328"],"synonyms":[{"name":"adenocarcinoma of minor salivary gland","type":"exact"},{"name":"adenocarcinoma of the minor salivary gland","type":"exact"}],"termid":"MONDO:0006304","xrefs":{"Monarch":{"xref_id":"0006304"}}}


id: PBO:0072897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SR-related CTD associated factor 1","termid":"PBO:0072897"}


id: PBO:0109361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 1","termid":"PBO:0109361"}


id: PBO:0066801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 100","termid":"PBO:0066801"}


id: GO:0022842
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transport of a solute across a membrane via a narrow pore channel that may be gated or ungated.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"channel activity","termid":"GO:0015267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"narrow pore channel activity","termid":"GO:0022842"}


id: MONDO:0014084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2","termid":"MONDO:0018996"},{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"ataxia with oculomotor apraxia type 3","secondary_identifiers":["GARD:13112","MEDGEN:767604","DOID:0060557","OMIM:615217","UMLS:C3554690"],"synonyms":[{"name":"AOA3","type":"related"},{"name":"ataxia-oculomotor apraxia 3","type":"exact"},{"name":"ataxia-oculomotor apraxia type 3","type":"exact"},{"name":"ataxia-oculomotor apraxia-3","type":"related"}],"termid":"MONDO:0014084","xrefs":{"Monarch":{"xref_id":"0014084"}}}


id: SO:0000262
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A tRNA sequence that has a histidine anticodon, and a 3' histidine binding region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"histidine_tRNA_primary_transcript","termid":"SO:0000219"},{"relation_name":"is_a","term_name":"tRNA","termid":"SO:0000253"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidyl_tRNA","synonyms":[{"name":"histidyl tRNA","type":"exact"},{"name":"histidyl-transfer RNA","type":"exact"},{"name":"histidyl-transfer ribonucleic acid","type":"exact"}],"termid":"SO:0000262"}


id: PBO:0042158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine ligand 19","termid":"PBO:0042158"}


id: PBO:0077568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 274, pseudogene","termid":"PBO:0077568"}


id: PBO:0028399
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_ricinoleic_acid","termid":"PBO:0028399"}


id: FYPO:0001744
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 import of biotin into the cell is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abnormal biotin import","synonyms":[{"name":"abnormal biotin import across plasma membrane","type":"exact"},{"name":"abnormal biotin import during mitotic cell cycle","type":"related"},{"name":"abnormal biotin import during vegetative growth","type":"exact"},{"name":"abnormal biotin import into cell","type":"exact"},{"name":"abnormal biotin uptake","type":"exact"}],"termid":"FYPO:0001744"}


id: PBO:0001620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribose-phosphate pyrophosphokinase (predicted)","termid":"PBO:0001620"}


id: GO:0060208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The estrous cycle phase in which there is heightened follicular activity.","definition_xrefs":["GOC:dph","ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"estrous cycle phase","termid":"GO:0060206"}],"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":"proestrus","termid":"GO:0060208"}


id: PBO:0049179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GREB1L divergent transcript","termid":"PBO:0049179"}


id: MONDO:0007293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leukocyte adhesion deficiency type I (LAD-I) is a form of LAD characterized by life-threatening, recurrent bacterial infections.","definition_xrefs":["Orphanet:99842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte adhesion deficiency","termid":"MONDO:0017570"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"leukocyte adhesion deficiency 1","secondary_identifiers":["GARD:6893","DOID:0110910","MEDGEN:98310","SCTID:234582006","UMLS:C0398738","NCIT:C4689","OMIM:116920","MESH:C535887"],"synonyms":[{"name":"ITGB2 leukocyte adhesion deficiency","type":"exact"},{"name":"LAD-I","type":"exact"},{"name":"LAD1","type":"exact"},{"name":"LFA 1 immunodeficiency","type":"related"},{"name":"LFA-I deficiency","type":"exact"},{"name":"LFA1 immunodeficiency","type":"exact"},{"name":"Lad1","type":"related"},{"name":"Lfa1 immunodeficiency","type":"related"},{"name":"lad","type":"related"},{"name":"lad 1","type":"related"},{"name":"lad-I","type":"exact"},{"name":"lad-type I","type":"exact"},{"name":"leukocyte adhesion deficiency","type":"broad"},{"name":"leukocyte adhesion deficiency 1","type":"exact"},{"name":"leukocyte adhesion deficiency caused by mutation in ITGB2","type":"exact"},{"name":"leukocyte adhesion deficiency type 1","type":"exact"},{"name":"leukocyte adhesion deficiency type I","type":"exact"},{"name":"leukocyte adhesion deficiency, type 1","type":"related"},{"name":"leukocyte adhesion deficiency, type I","type":"related"},{"name":"lymphocyte function-associated antigen 1 immunodeficiency","type":"exact"}],"termid":"MONDO:0007293","xrefs":{"Monarch":{"xref_id":"0007293"}}}


id: SO:0000973
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A terminal_inverted_repeat_element that is bacterial and only encodes the functions required for its transposition between these inverted repeats.","definition_xrefs":["SO:as"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insertion_sequence","secondary_identifiers":["http://en.wikipedia.org/wiki/Insertion_sequence"],"synonyms":[{"name":"IS","type":"related"},{"name":"insertion sequence","type":"exact"}],"termid":"SO:0000973"}


id: GO:0061327
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the anterior Malpighian tubule over time, from its formation to the mature structure. The pair of anterior tubules arise from a dorsal region of the embryonic hindgut and projects forwards through the body cavity. A Malpighian tubule is a fine, thin-walled excretory tubule in insects which connects with the posterior part of the gut.","definition_xrefs":["GOC:mtg_kidney_jan10","PMID:19783135","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Malpighian tubule development","termid":"GO:0072002"}],"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":"anterior Malpighian tubule development","termid":"GO:0061327"}


id: FYPO:0001836
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the spindle pole body is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to cytoskeleton","termid":"FYPO:0004096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to spindle pole body","synonyms":[{"name":"normal protein localisation to spindle pole body","type":"exact"},{"name":"normal protein localization to SPB","type":"exact"}],"termid":"FYPO:0001836"}


id: GO:0040028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of development of the vulva. Vulval development is the process whose specific outcome is the progression of the egg-laying organ of female and hermaphrodite nematodes over time, from its formation to the mature structure. In nematodes, the vulva is formed from ventral epidermal cells during larval stages to give rise to a fully formed vulva in the adult.","definition_xrefs":["GOC:ma","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"vulval development","termid":"GO:0040025"}],"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 vulval development","termid":"GO:0040028"}


id: MONDO:0032936
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myopathy, congenital, with respiratory insufficiency and bone fractures","secondary_identifiers":["MEDGEN:1718097","UMLS:C5394189","OMIM:618822","DOID:0081343"],"synonyms":[{"name":"MYOPATHY, CONGENITAL, WITH RESPIRATORY INSUFFICIENCY AND BONE FRACTURES","type":"related"},{"name":"MYORIBF","type":"related"}],"termid":"MONDO:0032936","xrefs":{"Monarch":{"xref_id":"0032936"}}}


id: GO:0047535
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-butyne-1,4-diol + NAD+ = 4-hydroxy-2-butynal + H+ + NADH.","definition_xrefs":["RHEA:19101","EC:1.1.1.165"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"2-alkyn-1-ol dehydrogenase activity","secondary_identifiers":["MetaCyc:2-ALKYN-1-OL-DEHYDROGENASE-RXN","KEGG_REACTION:R03963"],"synonyms":[{"name":"2-butyne-1,4-diol:NAD+ 1-oxidoreductase activity","type":"related"}],"termid":"GO:0047535"}


id: GO:0100034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that regulates 4,6-pyruvylated galactose residue biosynthetic process.","definition_xrefs":["GOC:obol","GOC:cjm"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of 4,6-pyruvylated galactose residue biosynthetic process by transcription from RNA polymerase II promoter (obsolete GO:0100034)","termid":"GO:0100034"}


id: GO:0010541
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The unidirectional movement of auxin from the base towards the apex of an organ, including the shoot, leaf, primary root, or lateral root.","definition_xrefs":["PMID:10677441"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxin polar transport","termid":"GO:0009926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"acropetal auxin transport","termid":"GO:0010541"}


id: PBO:0111464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA N1-methyladenine (m1A58) demethylase","termid":"PBO:0111464"}


id: MONDO:0800381
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":"46,XX true hermaphroditism, SRY-positive","termid":"MONDO:0800381","xrefs":{"Monarch":{"xref_id":"0800381"}}}


id: GO:0070681
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A tRNA aminoacylation process in which glutaminyl-tRNAGln is formed by a tRNA-dependent two-step pathway. In the first step a non-discriminating glutamyl-tRNAGlx synthetase generates the misacylated L-glutamyl-tRNAGln species, and in the second step it is amidated to the correctly charged L-glutaminyl-tRNAGln by a glutamyl-tRNAGln amidotransferase.","definition_xrefs":["MetaCyc:PWY-5921","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA aminoacylation","termid":"GO:0043039"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0006399"],"is_obsolete":false,"name":"glutaminyl-tRNAGln biosynthesis via transamidation","termid":"GO:0070681"}


id: PBO:0091334
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatase Z Homolog","termid":"PBO:0091334"}


id: GO:1904888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a cranial skeletal system over time, from its formation to the mature structure. The cranial skeletal system is the skeletal subdivision of the head, and includes the skull (cranium plus mandible), pharyngeal and/or hyoid apparatus.","definition_xrefs":["PMID:11262227","GOC:PARL","GOC:bf","GOC:TermGenie","GO_REF:0000094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cranial skeletal system development","synonyms":[{"name":"cranial skeleton development","type":"narrow"},{"name":"craniofacial development","type":"narrow"},{"name":"cranium development","type":"related"},{"name":"osteocranium development","type":"narrow"}],"termid":"GO:1904888"}


id: GO:0032918
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of spermidine by addition of acetyl groups.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spermidine metabolic process","termid":"GO:0008216"},{"relation_name":"is_a","term_name":"polyamine acetylation","termid":"GO:0032917"}],"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":"spermidine acetylation","termid":"GO:0032918"}


id: MONDO:0017702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete glycerol kinase deficiency (obsolete MONDO:0017702)","termid":"MONDO:0017702","xrefs":{"Monarch":{"xref_id":"0017702"}}}


id: PBO:0029981
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_mononucleate_monoseptate_vegetative_cell","termid":"PBO:0029981"}


id: GO:1905719
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within the perinuclear region of the cytoplasm.","definition_xrefs":["GOC:TermGenie","PMID:15177031","GO_REF:0000087"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization","termid":"GO:0008104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to perinuclear region of cytoplasm","synonyms":[{"name":"protein localisation in perinuclear region of cytoplasm","type":"exact"},{"name":"protein localisation to perinuclear region of cytoplasm","type":"exact"},{"name":"protein localization in perinuclear region of cytoplasm","type":"exact"},{"name":"protein localization to perinuclear cytoplasm","type":"exact"}],"termid":"GO:1905719"}


id: FYPO:0002586
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 tRNA 3'-end processing is normal (i.e. indistinguishable from wild type). In mitochondrial tRNA 3'-end processing, the 3' end of a mitochondrial pre-tRNA molecule is converted to that of a mature mitochondrial tRNA.","definition_xrefs":["GO:0006396","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA processing","termid":"FYPO:0001980"},{"relation_name":"is_a","term_name":"normal RNA metabolic process","termid":"FYPO:0004850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal mitochondrial tRNA 3'-end processing","synonyms":[{"name":"normal mitochondrial tRNA 3'-end processing during mitotic cell cycle","type":"related"},{"name":"normal mitochondrial tRNA 3'-end processing during vegetative growth","type":"exact"},{"name":"normal mitochondrial transfer RNA 3'-end processing","type":"exact"}],"termid":"FYPO:0002586"}


id: MONDO:1010796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Darier disease that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Darier disease, non-human animal","termid":"MONDO:1010153"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Darier disease, dog","secondary_identifiers":["OMIA:002265-9615"],"termid":"MONDO:1010796","xrefs":{"Monarch":{"xref_id":"1010796"}}}


id: PBO:0031297
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_multinucleate_vegetative_cell","termid":"PBO:0031297"}


id: PBO:0070851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13 pseudogene 4","termid":"PBO:0070851"}


id: MONDO:0022560
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare disorder that affects women with a history of uterine leiomyoma, which is found to metastasise within extrauterine sites.The disease develops as a proliferation of multiple nodules composed of smooth muscle cells.The most frequent site of metastasis is the lungs, although other areas may also be affected as well, including some atypical locations, e.g. the heart or spinal cord.","definition_xrefs":["PMID:28426767"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign metastasizing leiomyoma","secondary_identifiers":["MEDGEN:307261","UMLS:C1511090"],"termid":"MONDO:0022560","xrefs":{"Monarch":{"xref_id":"0022560"}}}


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


id: PBO:0045390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPP10 antisense RNA 1","termid":"PBO:0045390"}


id: PBO:0064950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 1","termid":"PBO:0064950"}


id: MOD:01884
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with a 4-aminobutyl group, usually derived from spermidine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkylated residue","termid":"MOD:00001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-aminobutylated residue","termid":"MOD:01884"}


id: GO:0016622
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which an aldehyde or ketone (oxo) group acts as a hydrogen or electron donor and reduces a cytochrome.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors","termid":"GO:0016903"}],"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":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, cytochrome as acceptor","secondary_identifiers":["EC:1.2.2.-"],"termid":"GO:0016622"}


id: PBO:0005131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma tubulin complex subunit Alp16","termid":"PBO:0005131"}


id: PBO:0081289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 72B, pseudogene","termid":"PBO:0081289"}


id: PBO:0057229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 384","termid":"PBO:0057229"}


id: MONDO:0005068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gross necrosis of the myocardium, as a result of interruption of the blood supply to the area, as in coronary thrombosis.","definition_xrefs":["NCIT:C27996"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"coronary artery disorder","termid":"MONDO:0005010"},{"relation_name":"is_a","term_name":"myocardial disorder","termid":"MONDO:0024643"}],"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":"myocardial infarction","secondary_identifiers":["EFO:0000612","ICD10CM:I21","SCTID:22298006","DOID:5844","MEDGEN:10150","UMLS:C0027051","NANDO:2200248","MESH:D009203","HP:0001658"],"synonyms":[{"name":"MI","type":"exact"},{"name":"MI, myocardial infarction","type":"exact"},{"name":"heart attack","type":"exact"},{"name":"infarction (MI), myocardial","type":"exact"},{"name":"myocardial infarct","type":"exact"},{"name":"myocardial infarction","type":"exact"},{"name":"myocardial infarction (disease)","type":"exact"},{"name":"myocardial infarction, (MI)","type":"exact"}],"termid":"MONDO:0005068","xrefs":{"Monarch":{"xref_id":"0005068"}}}


id: GO:0002436
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of immune complex clearance by monocytes or macrophages.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune complex clearance","termid":"GO:0002434"}],"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":"immune complex clearance by monocytes and macrophages","termid":"GO:0002436"}


id: PBO:0066240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 47","termid":"PBO:0066240"}


id: FYPO:0003296
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of ribosome binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein complex binding","termid":"FYPO:0005232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257","FYPO:0000702"],"is_obsolete":false,"name":"normal ribosome binding","termid":"FYPO:0003296"}


id: PBO:0043173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"corepressor interacting with RBPJ, CIR1","termid":"PBO:0043173"}


id: GO:0006711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of estrogens, C18 steroid hormones that can stimulate the development of female sexual characteristics. Also found in plants.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid catabolic process","termid":"GO:0006706"},{"relation_name":"is_a","term_name":"estrogen metabolic process","termid":"GO:0008210"},{"relation_name":"is_a","term_name":"hormone catabolic process","termid":"GO:0042447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"estrogen catabolic process","synonyms":[{"name":"estrogen breakdown","type":"exact"},{"name":"estrogen catabolism","type":"exact"},{"name":"estrogen degradation","type":"exact"},{"name":"oestrogen catabolic process","type":"exact"},{"name":"oestrogen catabolism","type":"exact"}],"termid":"GO:0006711"}


id: MONDO:0015852
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete excess breast volume or number (obsolete MONDO:0015852)","secondary_identifiers":["Orphanet:180170"],"termid":"MONDO:0015852","xrefs":{"Monarch":{"xref_id":"0015852"}}}


id: PBO:0091626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formamidase-like protein, implicated in cellular detoxification","termid":"PBO:0091626"}


id: GO:0060694
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, frequency, or extent of cholesterol transporter activity.","definition_xrefs":["GOC:dph","GOC:tb","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cholesterol transporter activity (obsolete GO:0060694)","termid":"GO:0060694"}


id: PBO:0087511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of heterodimeric peroxisomal ABC transport complex, with Pxa2p; required for import of long-chain fatty acids into peroxisomes; similar to human adrenoleukodystrophy transporters ABCD1and ABCD2, and ALD-related proteins; mutations in ABCD1 cause X-linked adrenoleukodystrophy (X-ALD), a peroxisomal disorder; human ABCD1 and ABCD2 can each partially complement yeast pxa1 pxa2 double null mutant","termid":"PBO:0087511"}


id: MONDO:0015618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic pancreatic disease (obsolete MONDO:0015618)","secondary_identifiers":["Orphanet:165661"],"termid":"MONDO:0015618","xrefs":{"Monarch":{"xref_id":"0015618"}}}


id: PBO:0035860
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_protein_movement_within_plasma_membrane_at_cell_tip","termid":"PBO:0035860"}


id: PBO:0085418
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; confers resistance to short-chain monocarboxylic acids and quinidine; involved in the excretion of excess amino acids; AQR1 has a paralog, QDR1, that arose from the whole genome duplication; relocalizes from plasma membrane to cytoplasm upon DNA replication stress","termid":"PBO:0085418"}


id: GO:0010550
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the chemical reactions and pathways resulting in the breakdown of one or more components of the light-harvesting complex of photosystem II.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein catabolic process","termid":"GO:0042176"},{"relation_name":"regulates","term_name":"PSII associated light-harvesting complex II catabolic process","termid":"GO:0010304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0030163"],"is_obsolete":false,"name":"regulation of PSII associated light-harvesting complex II catabolic process","synonyms":[{"name":"regulation of LHCII catabolism","type":"exact"},{"name":"regulation of LHCII degradation","type":"exact"}],"termid":"GO:0010550"}


id: MONDO:0018332
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple acyl-CoA dehydrogenase deficiency","termid":"MONDO:0009282"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005066","MONDO:0002525","MONDO:0004069"],"is_obsolete":false,"name":"multiple acyl-CoA dehydrogenase deficiency, severe neonatal type","secondary_identifiers":["MEDGEN:1842925","UMLS:C5680029","Orphanet:394529","GARD:17626"],"synonyms":[{"name":"MAD deficiency, severe neonatal type","type":"exact"},{"name":"MADD, severe neonatal type","type":"exact"},{"name":"glutaric aciduria type 2, severe neonatal type","type":"exact"}],"termid":"MONDO:0018332","xrefs":{"Monarch":{"xref_id":"0018332"}}}


id: PBO:0068213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 520","termid":"PBO:0068213"}


id: FYPO:0000049
data:
  {"alleles_by_uniquename":{"SJAG_00370:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00370","name":"erg1delta","uniquename":"SJAG_00370:allele-1"},"SJAG_00409:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00409","name":"gpd1delta","uniquename":"SJAG_00409:allele-1"},"SJAG_00871:allele-1":{"allele_type":"amino_acid_mutation","description":"cut3-T19E","gene_uniquename":"SJAG_00871","name":"cut3-T19E","uniquename":"SJAG_00871:allele-1"},"SJAG_03360:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03360","name":"shc1delta","uniquename":"SJAG_03360:allele-1"},"SJAG_04332:allele-1":{"allele_type":"amino_acid_mutation","description":"I30T,T572P","gene_uniquename":"SJAG_04332","name":"cdc25-D9","uniquename":"SJAG_04332:allele-1"},"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"},"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":{"multi_locus_phenotype":[{"annotations":[121373],"is_not":false,"summary":null,"term":"FYPO:0000049"},{"annotations":[121557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001489"}],"single_locus_phenotype":[{"annotations":[121349],"is_not":false,"rel_names":["has_part","is_a"],"summary":null,"term":"FYPO:0008029"},{"annotations":[121427],"is_not":false,"rel_names":["has_part","is_a"],"summary":null,"term":"FYPO:0007701"},{"annotations":[121152],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001489"},{"annotations":[121554],"is_not":false,"rel_names":["is_a","has_part"],"summary":null,"term":"FYPO:0003976"}]},"cv_name":"fission_yeast_phenotype","definition":"A viability phenotype in which a cell is unable to survive under conditions in which wild type cells survive.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell viability","termid":"FYPO:0000004"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00370":null,"SJAG_00409":null,"SJAG_00871":null,"SJAG_03360":null,"SJAG_04332":null,"SJAG_04464":null,"SJAG_04697":null},"genotype_count":6,"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"}]}]},"cut3-T19E-cut3-T19E-amino_acid_mutation-expression-not_assayed_or_wild_type__pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cut3-T19E(aa) 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shc1delta","display_uniquename":"erg1delta__shc1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00370:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03360:allele-1","expression":"Null"}]}]},"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]},"gpd1delta":{"display_name":"gpd1delta","display_uniquename":"gpd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00409:allele-1","expression":"Null"}]}]},"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000004"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_00370","SJAG_00871","SJAG_04464","SJAG_03360"],"name":"inviable cell","references_by_uniquename":{"PMID:25866389":null,"PMID:28954740":null,"PMID:36058798":null,"PMID:37164017":null,"PMID:40195311":null},"single_locus_annotated_genes":["SJAG_04332","SJAG_00409","SJAG_04697","SJAG_04464"],"single_locus_genotype_uniquenames":["pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type","gpd1delta","gms1delta"],"synonyms":[{"name":"lethal in cell","type":"exact"}],"termid":"FYPO:0000049","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYPO:0000049":null,"FYPO:0001489":null,"FYPO:0003976":null,"FYPO:0007701":null,"FYPO:0008029":null,"FYPO_EXT:0000001":null}}


id: PBO:0065329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 53","termid":"PBO:0065329"}


id: PATO:0000052
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphological quality inhering in a bearer by virtue of the bearer's ratios of distances between its features (points, edges, surfaces and also holes etc).","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphology","termid":"PATO:0000051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shape","secondary_identifiers":["PATO:0001647"],"synonyms":[{"name":"relational shape quality","type":"exact"}],"termid":"PATO:0000052"}


id: GO:0045345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of MHC class I.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of macromolecule biosynthetic process","termid":"GO:0010557"},{"relation_name":"is_a","term_name":"regulation of MHC class I biosynthetic process","termid":"GO:0045343"},{"relation_name":"positively_regulates","term_name":"MHC class I biosynthetic process","termid":"GO:0045341"}],"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 MHC class I biosynthetic process","synonyms":[{"name":"activation of MHC class I biosynthetic process","type":"narrow"},{"name":"positive regulation of MHC class I anabolism","type":"exact"},{"name":"positive regulation of MHC class I biosynthesis","type":"exact"},{"name":"positive regulation of MHC class I formation","type":"exact"},{"name":"positive regulation of MHC class I synthesis","type":"exact"},{"name":"positive regulation of major histocompatibility complex class I biosynthesis","type":"exact"},{"name":"positive regulation of major histocompatibility complex class I biosynthetic process","type":"exact"},{"name":"stimulation of MHC class I biosynthetic process","type":"narrow"},{"name":"up regulation of MHC class I biosynthetic process","type":"exact"},{"name":"up-regulation of MHC class I biosynthetic process","type":"exact"},{"name":"upregulation of MHC class I biosynthetic process","type":"exact"}],"termid":"GO:0045345"}


id: GO:0009927
data:
  {"annotated_genes":["SJAG_06592","SJAG_00331"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70242,79653],"is_not":false,"summary":null,"term":"GO:0009927"}]},"cv_name":"molecular_function","definition":"Serves as a phospho-His intermediate enabling the transfer of phospho group between a hybrid kinase and a response regulator.","definition_xrefs":["PMID:11842140","PMID:31386843"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase activity","termid":"GO:0004672"},{"relation_name":"is_a","term_name":"molecular transducer activity","termid":"GO:0060089"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00331":null,"SJAG_06592":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003674","GO:0004672","GO:0016740","GO:0016301","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"histidine phosphotransfer kinase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"termid":"GO:0009927","terms_by_termid":{"GO:0009927":null}}


id: MONDO:0019296
data:
  {"annotated_genes":["SJAG_00031","SJAG_01926"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88522],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007908"},{"annotations":[87365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011213"}]},"cv_name":"mondo","definition":"A disease involving the superficial fascia.","definition_xrefs":["MONDO:patterns/location_top"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare genetic skin disease (obsolete MONDO:0019043)","termid":"MONDO:0019043"},{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00031":null,"SJAG_01926":null},"genotype_count":0,"is_obsolete":false,"name":"subcutaneous tissue disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:712397","Orphanet:79382","UMLS:C1290008"],"synonyms":[{"name":"disease of superficial fascia","type":"exact"},{"name":"disease or disorder of superficial fascia","type":"exact"},{"name":"disorder of superficial fascia","type":"exact"},{"name":"superficial fascia disease","type":"exact"},{"name":"superficial fascia disease or disorder","type":"exact"}],"termid":"MONDO:0019296","terms_by_termid":{"MONDO:0007908":null,"MONDO:0011213":null},"xrefs":{"Monarch":{"xref_id":"0019296"}}}


id: GO:0046106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of thymine, 5-methyluracil, one of the two major pyrimidine bases present (as thymidine) in DNA but not found in RNA other than (as ribothymidine) in transfer RNA, where it is a minor base.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleobase biosynthetic process","termid":"GO:0019856"},{"relation_name":"is_a","term_name":"thymine metabolic process","termid":"GO:0019859"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"thymine biosynthetic process","synonyms":[{"name":"thymine anabolism","type":"exact"},{"name":"thymine biosynthesis","type":"exact"},{"name":"thymine formation","type":"exact"},{"name":"thymine synthesis","type":"exact"}],"termid":"GO:0046106"}


id: MONDO:0049222
data:
  {"annotated_genes":["SJAG_05326"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87749],"is_not":false,"summary":null,"term":"MONDO:0049222"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05326":null},"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 107","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1639885","GARD:22698","OMIM:301013","DOID:0112054","UMLS:C4692652"],"synonyms":[{"name":"MRX107","type":"related"},{"name":"intellectual developmental disorder, X-linked 107","type":"exact"},{"name":"intellectual disability, X-linked 107","type":"exact"},{"name":"mental retardation, X-linked 107","type":"related"}],"termid":"MONDO:0049222","terms_by_termid":{"MONDO:0049222":null},"xrefs":{"Monarch":{"xref_id":"0049222"}}}


id: GO:0090021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of Wnt protein to a frizzled family receptor on the surface of the target cell and increasing the rate or extent of posterior neural plate formation.","definition_xrefs":["GOC:sdb_2009","GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of posterior neural plate formation by Wnt signaling pathway (obsolete GO:0090021)","synonyms":[{"name":"positive regulation of posterior neural plate formation by Wnt receptor signaling pathway","type":"exact"},{"name":"positive regulation of posterior neural plate formation by Wnt receptor signalling pathway","type":"exact"},{"name":"positive regulation of posterior neural plate formation by Wnt-activated signaling pathway","type":"exact"}],"termid":"GO:0090021"}


id: MONDO:1011961
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachygnathia, cardiomegaly and renal hypoplasia syndrome, non-human animal","secondary_identifiers":["OMIA:001595"],"termid":"MONDO:1011961","xrefs":{"Monarch":{"xref_id":"1011961"}}}


id: PR:O14092
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 5-aminolevulinate synthase, erythroid-specific, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR13693:SF7","OMA:SCHPO01637"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-aminolevulinate synthase, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2F3.09","secondary_identifiers":["UniProtKB:O14092"],"synonyms":[{"name":"5-aminolevulinic acid synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ALAS2","type":"exact"},{"name":"delta-ALA synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"delta-aminolevulinate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14092"}


id: PBO:0044293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CXXC finger protein 1 pseudogene 1","termid":"PBO:0044293"}


id: GO:1901524
data:
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id: GO:0032559
data:
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of non-chaperonin molecular chaperone ATPase activity","type":"related"},{"name":"inhibition of protein complex assembly, multichaperone pathway","type":"related"},{"name":"inhibition of protein folding","type":"narrow"},{"name":"negative regulation of alpha-tubulin folding","type":"narrow"},{"name":"negative regulation of beta-tubulin folding","type":"narrow"},{"name":"negative regulation of chaperone activity","type":"related"},{"name":"negative regulation of chaperonin ATPase activity","type":"related"},{"name":"negative regulation of chaperonin-mediated tubulin folding","type":"narrow"},{"name":"negative regulation of co-chaperone activity","type":"related"},{"name":"negative regulation of co-chaperonin activity","type":"related"},{"name":"negative regulation of glycoprotein-specific chaperone activity","type":"related"},{"name":"negative regulation of non-chaperonin molecular chaperone ATPase activity","type":"related"},{"name":"negative regulation of protein complex assembly, multichaperone pathway","type":"related"}],"termid":"GO:1903333"}


id: PBO:0051857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster assembly 1 pseudogene 3","termid":"PBO:0051857"}


id: PBO:0056901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIER family member 3","termid":"PBO:0056901"}


id: PBO:0047179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 199, Y-linked, pseudogene","termid":"PBO:0047179"}


id: MONDO:0007463
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":"distal osteosclerosis","secondary_identifiers":["UMLS:C1852063","MEDGEN:338863","OMIM:126250","MESH:C565093"],"synonyms":[{"name":"distal osteosclerosis","type":"exact"},{"name":"osteosclerosis, distal","type":"related"}],"termid":"MONDO:0007463","xrefs":{"Monarch":{"xref_id":"0007463"}}}


id: PBO:0028396
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_27S_rRNA_precursor_level","termid":"PBO:0028396"}


id: PBO:0071244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 85","termid":"PBO:0071244"}


id: PBO:0005006
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cullin-associated Methyltransferase complex subunit","termid":"PBO:0005006"}


id: PBO:0054674
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 2080","termid":"PBO:0054674"}


id: MONDO:0017674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disease in which focal palmoplantar keratoderma is a major feature..","gene_count":0,"genotype_count":0,"name":"obsolete disease with focal palmoplantar keratoderma as a major feature (obsolete MONDO:0017674)","secondary_identifiers":["Orphanet:307871"],"synonyms":[{"name":"disease with focal palmoplantar hyperkeratosis as a major feature","type":"exact"}],"termid":"MONDO:0017674","xrefs":{"Monarch":{"xref_id":"0017674"}}}


id: PBO:0043322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAP-Gly domain containing linker protein family member 4","termid":"PBO:0043322"}


id: GO:0036040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of the polyphenol, curcumin.","definition_xrefs":["PMID:21467222"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"curcumin metabolic process","termid":"GO:0036039"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"olefinic compound catabolic process","termid":"GO:0120256"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"curcumin catabolic process","synonyms":[{"name":"(1E,6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione breakdown","type":"exact"},{"name":"(1E,6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione catabolic process","type":"exact"},{"name":"(1E,6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione catabolism","type":"exact"},{"name":"(1E,6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione degradation","type":"exact"},{"name":"curcumin breakdown","type":"exact"},{"name":"curcumin catabolism","type":"exact"},{"name":"curcumin degradation","type":"exact"},{"name":"diferuloylmethane breakdown","type":"exact"},{"name":"diferuloylmethane catabolic process","type":"exact"},{"name":"diferuloylmethane catabolism","type":"exact"},{"name":"diferuloylmethane degradation","type":"exact"},{"name":"turmeric yellow breakdown","type":"exact"},{"name":"turmeric yellow catabolic process","type":"exact"},{"name":"turmeric yellow catabolism","type":"exact"},{"name":"turmeric yellow degradation","type":"exact"}],"termid":"GO:0036040"}


id: GO:0033518
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of removing one or more phosphate group from myo-inositol hexakisphosphate.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete myo-inositol hexakisphosphate dephosphorylation (obsolete GO:0033518)","synonyms":[{"name":"phytate dephosphorylation","type":"exact"}],"termid":"GO:0033518"}


id: GO:0010180
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a thioglucosidase enzyme.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"thioglucosidase binding","synonyms":[{"name":"myrosinase binding","type":"exact"}],"termid":"GO:0010180"}


id: GO:0015258
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"gene_count":0,"genotype_count":0,"name":"obsolete gluconate channel activity (obsolete GO:0015258)","synonyms":[{"name":"gluconate channel activity","type":"exact"}],"termid":"GO:0015258"}


id: MONDO:0012260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract that has material basis in variation in the region 19q13.","definition_xrefs":["DOID:0110261","PMID:15671291"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset nuclear cataract","termid":"MONDO:0020376"}],"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":"cataract 35","secondary_identifiers":["MEDGEN:373050","OMIM:609376","UMLS:C1836272","MESH:C563728","GARD:9492"],"synonyms":[{"name":"CATCN1","type":"exact"},{"name":"CTRCT35","type":"exact"},{"name":"autosomal recessive congenital nuclear cataract 1","type":"exact"},{"name":"cataract 35","type":"exact"},{"name":"cataract 35, congenital nuclear","type":"exact"},{"name":"cataract type 35","type":"exact"},{"name":"cataract, congenital nuclear, autosomal recessive 1","type":"related"}],"termid":"MONDO:0012260","xrefs":{"Monarch":{"xref_id":"0012260"}}}


id: GO:0061176
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Terminal inflated portion of the axon of a glutamatergic neuron, containing the specialized apparatus necessary for the tonic release neurotransmitters that will induce the contraction of muscle. Type Ib terminal boutons are larger than type Is terminal boutons.","definition_xrefs":["GOC:mc","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"type I terminal bouton","termid":"GO:0061174"}],"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":"type Ib terminal bouton","synonyms":[{"name":"type Ib terminal button","type":"exact"}],"termid":"GO:0061176"}


id: GO:0075705
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The uptake of a virus into a host cell that begins by invagination of a specific region of the host cell plasma membrane around the bound virus to form a clathrin-coated pit, which then pinches off to form a clathrin-coated endocytic vesicles containing the virus. The vesicle then delivers its viral content to early endosomes, and the process ends when the viral nucleic acid is released into the host cytoplasm by its injection through the endosome membrane.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete viral entry into host cell via clathrin-mediated endocytosis followed by genetic injection through the endosome membrane (obsolete GO:0075705)","synonyms":[{"name":"viral entry into host cell via clathrin-mediated endocytosis followed by genetic injection through the endosome membrane","type":"exact"},{"name":"viral penetration via endocytosis followed by genetic injection through the endosome membrane","type":"exact"}],"termid":"GO:0075705"}


id: PBO:0046685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation termination factor 1 pseudogene 3","termid":"PBO:0046685"}


id: MONDO:0011562
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A late onset Parkinson disease that has material basis in heterozygous triplication of the alpha-synuclein gene (SNCA) on chromosome 4q22.","definition_xrefs":["PMID:14755720","DOID:0060895","PMID:17251522"],"direct_ancestors":[{"relation_name":"is_a","term_name":"late-onset Parkinson disease","termid":"MONDO:0008199"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal dominant Parkinson disease 4","secondary_identifiers":["MEDGEN:381361","UMLS:C1854182","GARD:18475","MESH:C565324","OMIM:605543"],"synonyms":[{"name":"PARK4","type":"related"},{"name":"Parkinson disease 4, autosomal dominant","type":"related"},{"name":"Parkinson disease 4, autosomal dominant Lewy body","type":"related"},{"name":"autosomal dominant Lewy body Parkinson disease 4","type":"exact"},{"name":"autosomal dominant Parkinson disease 4","type":"exact"},{"name":"autosomal dominant Parkinson disease type 4","type":"exact"},{"name":"autosomal dominant Parkinson's disease 4","type":"related"}],"termid":"MONDO:0011562","xrefs":{"Monarch":{"xref_id":"0011562"}}}


id: MONDO:0013113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any metaphyseal anadysplasia in which the cause of the disease is a mutation in the MMP9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metaphyseal anadysplasia","termid":"MONDO:0015177"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaphyseal anadysplasia 2","secondary_identifiers":["OMIM:613073","UMLS:C2751322","MEDGEN:414350","MESH:C567771","GARD:15610"],"synonyms":[{"name":"MANDP2","type":"related"},{"name":"MMP9 metaphyseal anadysplasia","type":"exact"},{"name":"metaphyseal anadysplasia 2","type":"exact"},{"name":"metaphyseal anadysplasia caused by mutation in MMP9","type":"exact"},{"name":"metaphyseal anadysplasia type 2","type":"exact"}],"termid":"MONDO:0013113","xrefs":{"Monarch":{"xref_id":"0013113"}}}


id: FYPO:0007071
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 rate, or speed, of mitotic spindle elongation is increased during anaphase a.","definition_xrefs":["PomBase:mah","PMID:31427431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased rate of mitotic spindle elongation","termid":"FYPO:0007958"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000054","FYPO:0005447","FYPO:0000641","FYPO:0000337","FYPO:0000631","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased rate of mitotic spindle elongation during anaphase A","synonyms":[{"name":"increased rate of mitotic spindle elongation during anaphase A during vegetative growth","type":"exact"},{"name":"increased rate of mitotic spindle elongation during mitotic anaphase A","type":"exact"},{"name":"increased rate of mitotic spindle extension during anaphase A","type":"exact"},{"name":"increased rate of spindle elongation during anaphase A of mitosis","type":"exact"}],"termid":"FYPO:0007071"}


id: MONDO:0030733
data:
  {"annotated_genes":["SJAG_02006"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88943],"is_not":false,"summary":null,"term":"MONDO:0030733"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02006":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 70","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070569","OMIM:619828","UMLS:C5676962","MEDGEN:1809945"],"synonyms":[{"name":"SPGF70","type":"exact"},{"name":"spermatogenic failure 70","type":"exact"}],"termid":"MONDO:0030733","terms_by_termid":{"MONDO:0030733":null},"xrefs":{"Monarch":{"xref_id":"0030733"}}}


id: MONDO:1010316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypophosphatasia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental defect during embryogenesis, non-human animal","termid":"MONDO:1011310"},{"relation_name":"is_a","term_name":"inborn errors of metabolism, non-human animal","termid":"MONDO:1012979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypophosphatasia, non-human animal","secondary_identifiers":["OMIA:002162"],"termid":"MONDO:1010316","xrefs":{"Monarch":{"xref_id":"1010316"}}}


id: GO:0004788
data:
  {"annotated_genes":["SJAG_03362"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79991],"is_not":false,"summary":null,"term":"GO:0004788"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + thiamine = AMP + thiamine diphosphate.","definition_xrefs":["RHEA:11576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diphosphotransferase activity","termid":"GO:0016778"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03362":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"thiamine diphosphokinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-196761","EC:2.7.6.2","MetaCyc:THIAMIN-PYROPHOSPHOKINASE-RXN"],"synonyms":[{"name":"ATP:thiamin pyrophosphotransferase activity","type":"related"},{"name":"ATP:thiamine diphosphotransferase activity","type":"related"},{"name":"TPTase activity","type":"related"},{"name":"thiamin diphosphokinase activity","type":"exact"},{"name":"thiamin pyrophosphokinase activity","type":"exact"},{"name":"thiamin pyrophosphotransferase activity","type":"related"},{"name":"thiamin:ATP pyrophosphotransferase activity","type":"related"},{"name":"thiamine pyrophosphokinase activity","type":"exact"},{"name":"thiaminokinase activity","type":"related"}],"termid":"GO:0004788","terms_by_termid":{"GO:0004788":null}}


id: FYPO:0003313
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an elongated germ tube, and in which the nucleus does not divide. The cell does not divide, and eventually dies.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, with elongated germ tube","termid":"FYPO:0002379"},{"relation_name":"is_a","term_name":"inviable elongated mononucleate vegetative cell","termid":"FYPO:0004255"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0001985","FYPO:0000005","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, mononucleate cell with elongated germ tube","synonyms":[{"name":"inviable after spore germination, without cell division, elongated mononucleate cell","type":"exact"},{"name":"inviable germinated spore, without cell division, mononucleate cell with elongated germ tube","type":"exact"},{"name":"inviable mononucleate germinated spore with elongated germ tube","type":"exact"},{"name":"lethal after spore germination, without cell division, mononucleate cell with elongated germ tube","type":"exact"},{"name":"mononucleate after spore germination with elongated germ tube","type":"exact"}],"termid":"FYPO:0003313"}


id: GO:0031381
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A virus-specific protein complex that possesses RNA-dependent RNA polymerase activity and replicates the genome of an RNA virus.","definition_xrefs":["PMID:15574411","GOC:mah","PMID:15613301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA-directed RNA polymerase complex","termid":"GO:0031379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"viral RNA-directed RNA polymerase complex","termid":"GO:0031381"}


id: PBO:0064741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 77","termid":"PBO:0064741"}


id: MONDO:0021451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the brain.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system organ benign neoplasm","termid":"MONDO:0000628"},{"relation_name":"is_a","term_name":"brain neoplasm","termid":"MONDO:0021211"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of brain","secondary_identifiers":["EFO:1000107","ICD9:225.0","NCIT:C4781","SCTID:92030004","UMLS:C0496899","MEDGEN:99225"],"synonyms":[{"name":"benign brain neoplasm","type":"exact"},{"name":"benign brain tumor","type":"exact"},{"name":"benign brain tumour","type":"exact"},{"name":"benign neoplasm of the brain","type":"exact"},{"name":"benign tumor of brain","type":"exact"},{"name":"benign tumor of the brain","type":"exact"},{"name":"benign tumour of brain","type":"exact"},{"name":"benign tumour of the brain","type":"exact"},{"name":"brain benign neoplasm","type":"exact"},{"name":"brain neoplasms, benign","type":"exact"}],"termid":"MONDO:0021451","xrefs":{"Monarch":{"xref_id":"0021451"}}}


id: PBO:0003403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pex16 family peroxisome import protein (predicted)","termid":"PBO:0003403"}


id: PR:O13811
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pdi2 gene.","definition_xrefs":["UniProtKB:O13811","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":"protein disulfide-isomerase C17H9.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17H9.14c","synonyms":[{"name":"Spom972h-pdi2","type":"exact"}],"termid":"PR:O13811"}


id: PBO:0002623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved ATP binding protein, implicated in sister chroamtid cohesion","termid":"PBO:0002623"}


id: GO:0019283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"he chemical reactions and pathways resulting in the formation of L-methionine from L-homoserine, via the intermediates O-phospho-L-homoserine and cystathionine.","definition_xrefs":["MetaCyc:PWY-702","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"},{"relation_name":"is_a","term_name":"organophosphate metabolic process","termid":"GO:0019637"},{"relation_name":"is_a","term_name":"'de novo' L-methionine biosynthetic process","termid":"GO:0071266"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid metabolic process","termid":"GO:0170041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0006790","GO:0044281"],"is_obsolete":false,"name":"L-methionine biosynthetic process from L-homoserine via O-phospho-L-homoserine and cystathionine","synonyms":[{"name":"L-methionine formation from O-phospho-L-homoserine and cystathionine","type":"exact"},{"name":"L-methionine synthesis from O-phospho-L-homoserine and cystathionine","type":"exact"},{"name":"methionine biosynthetic process from O-phospho-L-homoserine and cystathionine","type":"exact"}],"termid":"GO:0019283"}


id: PBO:0045327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dedicator of cytokinesis 6","termid":"PBO:0045327"}


id: GO:0055097
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by the detection of high density lipoprotein particle.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle mediated signaling","termid":"GO:0055095"},{"relation_name":"part_of","term_name":"cellular response to high density lipoprotein particle stimulus","termid":"GO:0071403"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"high density lipoprotein particle mediated signaling","synonyms":[{"name":"high density lipoprotein mediated signalling","type":"exact"},{"name":"high density lipoprotein particle mediated signal transduction","type":"exact"},{"name":"high density lipoprotein particle-mediated signaling","type":"exact"}],"termid":"GO:0055097"}


id: MONDO:1010663
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune thrombocytopenic purpura that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune thrombocytopenic purpura, non-human animal","termid":"MONDO:1010081"},{"relation_name":"is_a","term_name":"autoimmune thrombocytopenia, dog","termid":"MONDO:1010625"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune thrombocytopenic purpura, dog","secondary_identifiers":["OMIA:001104-9615"],"termid":"MONDO:1010663","xrefs":{"Monarch":{"xref_id":"1010663"}}}


id: PBO:0079110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA splicing endonuclease subunit 2","termid":"PBO:0079110"}


id: PBO:0065095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKAG2 antisense RNA 2","termid":"PBO:0065095"}


id: GO:0002068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a glandular epithelial cell over time, from its formation to the mature structure. A glandular epithelial cell is a columnar/cuboidal epithelial cell is a cell found in a two dimensional sheet with a free surface exposed to the lumen of a gland.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"columnar/cuboidal epithelial cell development","termid":"GO:0002066"},{"relation_name":"part_of","term_name":"glandular epithelial cell differentiation","termid":"GO:0002067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"glandular epithelial cell development","termid":"GO:0002068"}


