# terms

id: GO:0035609
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of a C-terminal, gene-encoded glutamate residue from a protein.","definition_xrefs":["PMID:21074048","GOC:sp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-terminal protein amino acid modification","termid":"GO:0018410"},{"relation_name":"is_a","term_name":"protein deglutamylation","termid":"GO:0035608"}],"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":"C-terminal protein deglutamylation","synonyms":[{"name":"protein primary sequence deglutamylation","type":"exact"}],"termid":"GO:0035609"}


id: PATO:0000560
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000560 height value (obsolete PATO:0000560)","termid":"PATO:0000560"}


id: GO:0102478
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-L-arabinofuranosyl-(1->2)-beta-L-arabinofuranose + H2O = 2 beta-L-arabinofuranose.","definition_xrefs":["GOC:pz","RHEA:36051"],"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:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0016798","GO:0003674"],"is_obsolete":false,"name":"beta-L-arabinofuranosidase activity","secondary_identifiers":["EC:3.2.1.185","MetaCyc:RXN-14089"],"termid":"GO:0102478"}


id: PBO:0074494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptosome associated protein 23","termid":"PBO:0074494"}


id: GO:0032010
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bounded intracellular vesicle formed by maturation of an early phagosome following the ingestion of particulate material by phagocytosis; during maturation, phagosomes acquire markers of late endosomes and lysosomes.","definition_xrefs":["GOC:mah","PMID:12388753","PMID:14733906"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary lysosome","termid":"GO:0005767"},{"relation_name":"is_a","term_name":"phagocytic vesicle","termid":"GO:0045335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005773"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005773","GO:0005737"],"is_obsolete":false,"name":"phagolysosome","secondary_identifiers":["Wikipedia:Phagolysosome"],"synonyms":[{"name":"late phagocytic vesicle","type":"related"},{"name":"late phagosome","type":"related"}],"termid":"GO:0032010"}


id: MONDO:0010018
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":"second metatarsal-metacarpal syndrome","secondary_identifiers":["MEDGEN:341415","MESH:C564824","OMIM:269630","UMLS:C1849259"],"synonyms":[{"name":"second metatarsal-metacarpal syndrome","type":"exact"}],"termid":"MONDO:0010018","xrefs":{"Monarch":{"xref_id":"0010018"}}}


id: PBO:0041304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2 calcium dependent domain containing 6","termid":"PBO:0041304"}


id: MONDO:0030525
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa simplex","termid":"MONDO:0017610"}],"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":"epidermolysis bullosa simplex 2B, generalized intermediate","secondary_identifiers":["UMLS:C5562009","MEDGEN:1794219","OMIM:619588"],"synonyms":[{"name":"EBS2B","type":"exact"}],"termid":"MONDO:0030525","xrefs":{"Monarch":{"xref_id":"0030525"}}}


id: MONDO:0004555
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An angiomyolipoma arising from the kidney.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney benign neoplasm","termid":"MONDO:0002513"},{"relation_name":"is_a","term_name":"angiomyolipoma","termid":"MONDO:0002603"},{"relation_name":"is_a","term_name":"benign PEComa","termid":"MONDO:0020581"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"kidney angiomyolipoma","secondary_identifiers":["ONCOTREE:RAML","SCTID:254921004","UMLS:C0241961","NCIT:C3888","DOID:8411","MEDGEN:69146"],"synonyms":[{"name":"RAML","type":"related"},{"name":"angiomyolipoma of kidney","type":"exact"},{"name":"angiomyolipoma of the kidney","type":"exact"},{"name":"kidney angiomyolipoma","type":"exact"},{"name":"renal angiomyolipoma","type":"exact"}],"termid":"MONDO:0004555","xrefs":{"Monarch":{"xref_id":"0004555"}}}


id: MONDO:0019930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Leydig cell hypoplasia, type 1","termid":"MONDO:0009384"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Leydig cell hypoplasia due to complete LH resistance","secondary_identifiers":["MEDGEN:1776152","Orphanet:96265","DOID:0112260","GARD:16851","UMLS:C5438974"],"synonyms":[{"name":"46,XY DSD due to complete LH receptor inactivation","type":"exact"},{"name":"46,XY DSD due to complete LH resistance","type":"exact"},{"name":"46,XY DSD due to complete luteinizing hormone receptor inactivation","type":"exact"},{"name":"46,XY DSD due to complete luteinizing hormone resistance","type":"exact"},{"name":"46,XY disorder of sex development due to complete LH receptor inactivation","type":"exact"},{"name":"46,XY disorder of sex development due to complete LH resistance","type":"exact"},{"name":"46,XY disorder of sex development due to complete luteinizing hormone receptor inactivation","type":"exact"},{"name":"46,XY disorder of sex development due to complete luteinizing hormone resistance","type":"exact"},{"name":"Leydig cell hypoplasia due to complete LH receptor inactivation","type":"exact"},{"name":"Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation","type":"exact"},{"name":"Leydig cell hypoplasia due to complete luteinizing hormone resistance","type":"exact"}],"termid":"MONDO:0019930","xrefs":{"Monarch":{"xref_id":"0019930"}}}


id: GO:0019432
data:
  {"annotated_genes":["SJAG_03162","SJAG_04041","SJAG_02763","SJAG_03609"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73268,76456,78944,91980],"is_not":false,"summary":null,"term":"GO:0019432"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a triglyceride, any triester of glycerol.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triglyceride metabolic process","termid":"GO:0006641"},{"relation_name":"is_a","term_name":"acylglycerol biosynthetic process","termid":"GO:0046463"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02763":null,"SJAG_03162":null,"SJAG_03609":null,"SJAG_04041":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"triglyceride biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-75109","MetaCyc:TRIGLSYN-PWY"],"synonyms":[{"name":"triacylglycerol biosynthesis","type":"exact"},{"name":"triacylglycerol biosynthetic process","type":"exact"},{"name":"triglyceride anabolism","type":"exact"},{"name":"triglyceride biosynthesis","type":"exact"},{"name":"triglyceride formation","type":"exact"},{"name":"triglyceride synthesis","type":"exact"}],"termid":"GO:0019432","terms_by_termid":{"GO:0019432":null}}


id: PBO:0068836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 74, pseudogene","termid":"PBO:0068836"}


id: GO:2000443
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of toll-like receptor 21 signaling pathway.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of toll-like receptor signaling pathway","termid":"GO:0034121"},{"relation_name":"regulates","term_name":"toll-like receptor 21 signaling pathway","termid":"GO:0035682"}],"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 toll-like receptor 21 signaling pathway","synonyms":[{"name":"regulation of TLR21 signaling pathway","type":"exact"},{"name":"regulation of toll-like receptor 21 signalling pathway","type":"exact"}],"termid":"GO:2000443"}


id: PBO:0053430
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 375","termid":"PBO:0053430"}


id: PBO:0062829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oncostatin M receptor","termid":"PBO:0062829"}


id: PBO:0042674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule pseudogene 8","termid":"PBO:0042674"}


id: PBO:0001979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BC10 family protein","termid":"PBO:0001979"}


id: GO:0051636
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to a component on the surface of a Gram-negative bacterial cell.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete Gram-negative bacterial cell surface binding (obsolete GO:0051636)","synonyms":[{"name":"Gram-negative bacterial binding","type":"exact"},{"name":"Gram-negative bacterial cell surface binding","type":"exact"},{"name":"Gram-negative bacterium binding","type":"exact"},{"name":"Gram-negative bacterium cell surface binding","type":"exact"},{"name":"binding to Gram-negative bacterium","type":"exact"}],"termid":"GO:0051636"}


id: PBO:0063392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"programmed cell death 6 interacting protein","termid":"PBO:0063392"}


id: PR:O74560
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- raf2 gene.","definition_xrefs":["UniProtKB:O74560","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":"rik1-associated factor 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC970.07c","synonyms":[{"name":"De-localization of swi6 protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-raf2","type":"exact"},{"name":"cryptic loci regulator 7 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74560"}


id: PBO:0080000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 10 pseudogene 1","termid":"PBO:0080000"}


id: PBO:0081276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 43","termid":"PBO:0081276"}


id: GO:0048441
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the petal over time, from its formation to the mature structure.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floral organ development","termid":"GO:0048437"},{"relation_name":"is_a","term_name":"phyllome development","termid":"GO:0048827"},{"relation_name":"part_of","term_name":"corolla development","termid":"GO:0048465"}],"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":"petal development","secondary_identifiers":["GO:0048417"],"termid":"GO:0048441"}


id: MONDO:0008418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"systemic sclerosis","termid":"MONDO:0005100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"scleroderma, familial progressive","secondary_identifiers":["MEDGEN:356661","UMLS:C1866983","OMIM:181750"],"synonyms":[{"name":"Crest syndrome","type":"related"},{"name":"scleroderma, familial progressive","type":"exact"},{"name":"systemic sclerosis, susceptibility to","type":"related"}],"termid":"MONDO:0008418","xrefs":{"Monarch":{"xref_id":"0008418"}}}


id: PBO:0029594
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_plasma_membrane_during_vegetative_growth","termid":"PBO:0029594"}


id: PBO:0076545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAT antisense RNA 1","termid":"PBO:0076545"}


id: RO:0003302
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between an entity (e.g. a genotype, genetic variation, chemical, or environmental exposure) and a condition (a phenotype or disease), where the entity has some causal or contributing role that influences the condition.","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_related_to","termid":"RO:0002410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causes_or_contributes_to_condition","termid":"RO:0003302"}


id: FYPO:0003820
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 fewer mitochondria than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"mitochondria present in decreased numbers during vegetative growth","synonyms":[{"name":"decreased number of mitochondria during vegetative growth","type":"exact"},{"name":"fewer mitochondria during vegetative growth","type":"exact"},{"name":"mitochondria present in decreased numbers during mitotic cell cycle","type":"related"},{"name":"mitochondria present in reduced numbers during vegetative growth","type":"exact"}],"termid":"FYPO:0003820"}


id: PBO:0002658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNP complex (predicted)","termid":"PBO:0002658"}


id: PBO:0039785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aquaporin 12A","termid":"PBO:0039785"}


id: PBO:0084568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Membrane protein involved in the synthesis of GlcNAc-PI; N-acetylglucosaminyl phosphatidylinositol (GlcNAc-PI) is the first intermediate in the synthesis of glycosylphosphatidylinositol (GPI) anchors; human and mouse GPI1 are functional homologs","termid":"PBO:0084568"}


id: MONDO:0017916
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pure or complex X-linked spastic paraplegia (obsolete MONDO:0017916)","secondary_identifiers":["Orphanet:320350"],"synonyms":[{"name":"Pure or complicated X-linked spastic paraplegia","type":"exact"}],"termid":"MONDO:0017916","xrefs":{"Monarch":{"xref_id":"0017916"}}}


id: PBO:0030350
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_kinetochore_during_vegetative_growth","termid":"PBO:0030350"}


id: FYPO:0004101
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 sister chromatids do not move towards the spindle poles at the same time during mitosis prior to completion of chromosome segregation. Although one or more chromosomes remain distant from the spindle pole after the bulk of the DNA has separated, mitotic sister chromatid segregation does eventually go on to complete separation of chromosomes.","definition_xrefs":["PMID:17561805","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lagging mitotic chromosomes","termid":"FYPO:0000228"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000641","FYPO:0001320","FYPO:0000337","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"lagging mitotic chromosomes, with complete sister chromatid separation","synonyms":[{"name":"chromosome segregation defects, lagging mitotic chromosomes, with complete sister chromatid separation","type":"exact"},{"name":"lagging chromosomes, with complete sister chromatid separation during mitotic cell cycle","type":"related"},{"name":"lagging chromosomes, with complete sister chromatid separation, during vegetative growth","type":"exact"},{"name":"lagging mitotic chromosomes, with complete chromosome separation","type":"exact"},{"name":"lagging mitotic sister chromatids, with complete sister chromatid separation","type":"exact"}],"termid":"FYPO:0004101"}


id: MONDO:0000082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormal descent of a pelvic organ resulting in the protrusion of the organ beyond its normal anatomical confines. Symptoms often include vaginal discomfort, dyspareunia; urinary stress incontinence; and fecal incontinence.","definition_xrefs":["MESH:D056887"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pelvic organ prolapse","secondary_identifiers":["icd11.foundation:148580117","EFO:0004710","SCTID:237113009","MEDGEN:209090","UMLS:C0877015"],"termid":"MONDO:0000082","xrefs":{"Monarch":{"xref_id":"0000082"}}}


id: PBO:0088940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [2Fe-2S] cluster assembly and type II fatty acid synthase component","termid":"PBO:0088940"}


id: GO:0009245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lipid A, the glycolipid group of bacterial lipopolysaccharides, consisting of four to six fatty acyl chains linked to two glucosamine residues. Further modifications of the backbone are common.","definition_xrefs":["PMID:22216004","ISBN:0198506732","PMID:20974832"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid biosynthetic process","termid":"GO:0008654"},{"relation_name":"is_a","term_name":"glycolipid biosynthetic process","termid":"GO:0009247"},{"relation_name":"is_a","term_name":"lipid A metabolic process","termid":"GO:0046493"},{"relation_name":"is_a","term_name":"lipooligosaccharide biosynthetic process","termid":"GO:1901271"}],"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":"lipid A biosynthetic process","secondary_identifiers":["MetaCyc:NAGLIPASYN-PWY"],"synonyms":[{"name":"lipid A anabolism","type":"exact"},{"name":"lipid A biosynthesis","type":"exact"},{"name":"lipid A formation","type":"exact"},{"name":"lipid A synthesis","type":"exact"}],"termid":"GO:0009245"}


id: GO:0019877
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of diaminopimelate, both as an intermediate in lysine biosynthesis and as a component (as meso-diaminopimelate) of the peptidoglycan of Gram-negative bacterial cell walls.","definition_xrefs":["GOC:ma","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid biosynthetic process","termid":"GO:0008652"},{"relation_name":"is_a","term_name":"dicarboxylic acid biosynthetic process","termid":"GO:0043650"},{"relation_name":"is_a","term_name":"diaminopimelate metabolic process","termid":"GO:0046451"},{"relation_name":"is_a","term_name":"fatty acid derivative biosynthetic process","termid":"GO:1901570"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"diaminopimelate biosynthetic process","synonyms":[{"name":"diaminopimelate anabolism","type":"exact"},{"name":"diaminopimelate biosynthesis","type":"exact"},{"name":"diaminopimelate formation","type":"exact"},{"name":"diaminopimelate synthesis","type":"exact"}],"termid":"GO:0019877"}


id: MONDO:0010304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Graves disease","termid":"MONDO:0005364"},{"relation_name":"is_a","term_name":"autoimmune thyroid disease, susceptibility to","termid":"MONDO:0000162"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Graves disease, susceptibility to, X-linked 1","secondary_identifiers":["UMLS:C2678151","OMIM:300351","MEDGEN:395552"],"synonyms":[{"name":"Graves disease, susceptibility to, X-linked","type":"exact"},{"name":"Graves disease, susceptibility to, X-linked 1","type":"exact"},{"name":"Graves disease, susceptibility to, X-linked 2","type":"related"},{"name":"Graves disease, susceptibility to, X-linked type 1","type":"exact"},{"name":"Grdx1","type":"related"}],"termid":"MONDO:0010304","xrefs":{"Monarch":{"xref_id":"0010304"}}}


id: GO:0140961
data:
  {"annotated_genes":["SJAG_02599","SJAG_01344","SJAG_01351","SJAG_00988","SJAG_03497","SJAG_04516"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72743,98998,120213,98960,110406,95253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098849"}]},"cv_name":"biological_process","definition":"Any process carried out at the cellular level that reduces or removes the toxicity of a metal ion.","definition_xrefs":["PMID:26729300","PMID:33046888","PMID:34442707"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detoxification of inorganic compound","termid":"GO:0061687"},{"relation_name":"is_a","term_name":"cellular detoxification","termid":"GO:1990748"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00988":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_02599":null,"SJAG_03497":null,"SJAG_04516":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"cellular detoxification of metal ion","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"cellular detoxification of metal cation","type":"exact"}],"termid":"GO:0140961","terms_by_termid":{"GO:0098849":null}}


id: GO:0016247
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and modulates the activity of a channel. A channel catalyzes energy-independent facilitated diffusion, mediated by passage of a solute through a transmembrane aqueous pore or channel.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transporter regulator activity","termid":"GO:0141108"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0003674","GO:0098772"],"is_obsolete":false,"name":"channel regulator activity","termid":"GO:0016247"}


id: MONDO:0017993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare but serious cerebrovascular disorder involving thrombosis of the cerebral venous system. It affects children from the newborn period through childhood and adolescence. In childhood CSVT, acute infections of the head and neck such as mastoiditis are most common, followed by chronic underlying diseases such as nephrotic syndrome, cancer, and inflammatory bowel disease. Signs and symptoms are also age related. Seizures and altered mental status are the commonest manifestations in newborns. Headache, vomiting, and lethargy, sometimes with 6th nerve palsy, are the most common symptoms in children and adolescents.","definition_xrefs":["PMID:28798906"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebrovascular disorder","termid":"MONDO:0011057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral sinovenous thrombosis","secondary_identifiers":["GARD:21485","Orphanet:329217"],"synonyms":[{"name":"CSVT","type":"exact"}],"termid":"MONDO:0017993","xrefs":{"Monarch":{"xref_id":"0017993"}}}


id: PBO:0052037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"jumping translocation breakpoint pseudogene 1","termid":"PBO:0052037"}


id: PBO:0064557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein O-mannose kinase","termid":"PBO:0064557"}


id: PBO:0029851
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_heterochromatin_at_centromere_outer_repeat","termid":"PBO:0029851"}


id: GO:0102133
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (4R)-limonene + O2 + NADH + H+ = (4R)-perillyl alcohol + NAD + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete limonene hydroxylase activity (obsolete GO:0102133)","termid":"GO:0102133"}


id: GO:0021652
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to rhombomere 1. This process pertains to the initial formation of a structure from unspecified parts. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates. Rhombomeres are numbered in anterior to posterior order.","definition_xrefs":["GO_REF:0000021","GOC:cls","GOC:curators","GOC:jid","GOC:dph","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhombomere formation","termid":"GO:0021594"},{"relation_name":"part_of","term_name":"rhombomere 1 morphogenesis","termid":"GO:0021651"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"rhombomere 1 formation","termid":"GO:0021652"}


id: GO:0016798
data:
  {"annotated_genes":["SJAG_02718","SJAG_01883","SJAG_02261","SJAG_02799","SJAG_01119","SJAG_02949","SJAG_02649","SJAG_02590","SJAG_03295","SJAG_00620","SJAG_03280","SJAG_03444","SJAG_03646","SJAG_02446","SJAG_02131","SJAG_04850","SJAG_05272","SJAG_04851","SJAG_04859","SJAG_01017","SJAG_02478","SJAG_01888","SJAG_01171","SJAG_04927","SJAG_04301","SJAG_00667","SJAG_01974","SJAG_02192","SJAG_00485","SJAG_02711","SJAG_00096","SJAG_03724","SJAG_04238","SJAG_04327","SJAG_01781","SJAG_01029","SJAG_02179","SJAG_01971","SJAG_00310","SJAG_00957","SJAG_03824","SJAG_04864","SJAG_01858","SJAG_03032","SJAG_05001","SJAG_04789","SJAG_02076","SJAG_02528","SJAG_02435","SJAG_04363"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034042"},{"annotations":[77664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070694"},{"annotations":[98099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034043"},{"annotations":[98100,76184,75451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034039"},{"annotations":[73370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004555"},{"annotations":[103557,103558],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004558"},{"annotations":[60840,65034,60207,69038,68004,62325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004556"},{"annotations":[69772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004557"},{"annotations":[90251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004559"},{"annotations":[89389,117628,110373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008422"},{"annotations":[80050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004568"},{"annotations":[103538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052820"},{"annotations":[103539],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008725"},{"annotations":[103540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043916"},{"annotations":[62905,71183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052861"},{"annotations":[89320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106407"},{"annotations":[80665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004573"},{"annotations":[60724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004339"},{"annotations":[58188,70258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051118"},{"annotations":[75981,79791,81946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042973"},{"annotations":[103906,75155,103907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046557"},{"annotations":[72481,72378,75152,97056,78946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004338"},{"annotations":[78688,77067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015926"},{"annotations":[64366,77908,90638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004553"},{"annotations":[58191,57808,58422,98880,64268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008496"},{"annotations":[68336,80644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004571"},{"annotations":[92600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070635"},{"annotations":[92601],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070636"},{"annotations":[77152,114168],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008477"},{"annotations":[75455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000701"},{"annotations":[100539,100540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106432"},{"annotations":[78692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004575"},{"annotations":[80171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004844"},{"annotations":[92603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045437"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any glycosyl bond.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase 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activity, acting on glycosyl bonds","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-2065233","EC:3.2.-.-","Reactome:R-HSA-1793176","Reactome:R-HSA-5333609"],"synonyms":[{"name":"N-glycosylase","type":"narrow"},{"name":"glycosidase 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id: PBO:0116733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRCA1 interacting DNA helicase 1","termid":"PBO:0116733"}


id: GO:1904428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of tubulin deacetylation.","definition_xrefs":["PMID:23886946","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein modification process","termid":"GO:0031400"},{"relation_name":"is_a","term_name":"regulation of tubulin deacetylation","termid":"GO:0090043"},{"relation_name":"negatively_regulates","term_name":"tubulin deacetylation","termid":"GO:0090042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of tubulin deacetylation","synonyms":[{"name":"down regulation of tubulin deacetylation","type":"exact"},{"name":"down-regulation of tubulin deacetylation","type":"exact"},{"name":"downregulation of tubulin deacetylation","type":"exact"},{"name":"inhibition of tubulin deacetylation","type":"narrow"}],"termid":"GO:1904428"}


id: GO:0099075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Vesicle-mediated transport of cargo from the mitochondrion by a mitochondrion-derived vesicle.","definition_xrefs":["GOC:PARL-UCL","PMID:20619655","GOC:bc","GOC:pad","PMID:37131163"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle-mediated transport","termid":"GO:0016192"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"mitochondrion-derived vesicle mediated transport","termid":"GO:0099075"}


id: MONDO:8000018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic recurrent vertigo associated with positional nystagmus. It is associated with a vestibular loss without other neurological or auditory signs. Unlike in labyrinthitis and vestibular neuronitis inflammation in the ear is not observed.","definition_xrefs":["MESH:D065635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral vertigo","termid":"MONDO:0004900"},{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"},{"relation_name":"is_a","term_name":"inherited auditory system disease","termid":"MONDO:0037940"},{"relation_name":"is_a","term_name":"hereditary neuromuscular disease","termid":"MONDO:0100546"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign paroxysmal positional vertigo","secondary_identifiers":["ICD9:386.11","OMIM:193007","DOID:13941","MEDGEN:57837","UMLS:C0155502","SCTID:111541001"],"synonyms":[{"name":"BPPV","type":"exact"},{"name":"BRV","type":"exact"},{"name":"benign paroxysmal positional nystagmus","type":"exact"},{"name":"benign paroxysmal positional vertigo","type":"exact"},{"name":"familial benign recurrent vertigo","type":"exact"},{"name":"familial vestibulopathy","type":"exact"},{"name":"vertigo, benign paroxysmal positional","type":"exact"},{"name":"vertigo, benign recurrent","type":"exact"},{"name":"vestibulopathy, familial","type":"exact"}],"termid":"MONDO:8000018","xrefs":{"Monarch":{"xref_id":"8000018"}}}


id: PBO:0076538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 67 pseudogene","termid":"PBO:0076538"}


id: GO:0018455
data:
  {"annotated_genes":["SJAG_02963","SJAG_03821","SJAG_01869","SJAG_03958","SJAG_00038","SJAG_03370","SJAG_02010","SJAG_01414","SJAG_00240","SJAG_03822","SJAG_04660","SJAG_03196","SJAG_01457","SJAG_00242","SJAG_00237","SJAG_01543"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73059,80021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004022"},{"annotations":[94419,79399,108508,108509],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008106"},{"annotations":[76197,93766],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004032"},{"annotations":[103142,97702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032866"},{"annotations":[116612,116611,100683,100684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120542"},{"annotations":[93769],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047018"},{"annotations":[103143,97703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032867"},{"annotations":[74507],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003939"},{"annotations":[116393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050236"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: an alcohol + NAD(P)+ = an aldehyde or ketone + NAD(P)H + H+.","definition_xrefs":["GOC:curators"],"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":16,"genes_by_uniquename":{"SJAG_00038":null,"SJAG_00237":null,"SJAG_00240":null,"SJAG_00242":null,"SJAG_01414":null,"SJAG_01457":null,"SJAG_01543":null,"SJAG_01869":null,"SJAG_02010":null,"SJAG_02963":null,"SJAG_03196":null,"SJAG_03370":null,"SJAG_03821":null,"SJAG_03822":null,"SJAG_03958":null,"SJAG_04660":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"alcohol dehydrogenase [NAD(P)+] activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"alcohol:NAD(P)+ oxidoreductase activity","type":"related"},{"name":"aldehyde reductase (NADPH/NADH)","type":"related"}],"termid":"GO:0018455","terms_by_termid":{"GO:0003939":null,"GO:0004022":null,"GO:0004032":null,"GO:0008106":null,"GO:0032866":null,"GO:0032867":null,"GO:0047018":null,"GO:0050236":null,"GO:0120542":null}}


id: MONDO:0033635
data:
  {"annotated_genes":["SJAG_03173"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87648],"is_not":false,"summary":null,"term":"MONDO:0033635"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex IV deficiency, nuclear-type","termid":"MONDO:0033885"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03173":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex 4 deficiency, nuclear type 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619046","UMLS:C5436682","DOID:0070492","GARD:16404","MEDGEN:1764816"],"synonyms":[{"name":"MC4DN3","type":"exact"},{"name":"mitochondrial complex IV deficiency, nuclear type 3","type":"exact"}],"termid":"MONDO:0033635","terms_by_termid":{"MONDO:0033635":null},"xrefs":{"Monarch":{"xref_id":"0033635"}}}


id: GO:0061961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency or rate of heme oxygenase activity.","definition_xrefs":["GOC:rph","GOC:BHF","GOC:BHF_miRNA","PMID:24844779"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of heme oxygenase activity (obsolete GO:0061961)","termid":"GO:0061961"}


id: MONDO:0958343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare autoinflammatory syndrome characterized by a chronic-relapsing course of the combination of pyogenic arthritis, pyoderma gangrenosum, acne, and hidradenitis suppurativa (which, in addition to axillae and inguinal folds, can be observed on the face, neck, scalp, back, and buttocks, among others). Typical age of onset is adolescence to young adulthood, with the different signs and symptoms appearing simultaneously or subsequently.","definition_xrefs":["Orphanet:641380"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAPASH syndrome","secondary_identifiers":["UMLS:C5816787","MEDGEN:1853140"],"termid":"MONDO:0958343","xrefs":{"Monarch":{"xref_id":"0958343"}}}


id: MONDO:0017621
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital sucrase-isomaltase deficiency","termid":"MONDO:0009114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"congenital sucrase-isomaltase deficiency with starch and lactose intolerance","secondary_identifiers":["Orphanet:306474"],"synonyms":[{"name":"CSID with starch and lactose intolerance","type":"exact"},{"name":"congenital sucrase-isomaltose malabsorption with starch and lactose intolerance","type":"exact"},{"name":"congenital sucrose intolerance with starch and lactose intolerance","type":"exact"},{"name":"disaccharide intolerance with starch and lactose intolerance","type":"exact"}],"termid":"MONDO:0017621","xrefs":{"Monarch":{"xref_id":"0017621"}}}


id: PBO:0084785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial phosphatidylglycerophosphatase (PGP phosphatase); dephosphorylates phosphatidylglycerolphosphate to generate phosphatidylglycerol, an essential step during cardiolipin biosynthesis; null mutant is sensitive to tunicamycin, DTT","termid":"PBO:0084785"}


id: GO:1902814
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:10499580","GOC:mr"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry (obsolete GO:1902814)","synonyms":[{"name":"activation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"narrow"},{"name":"activation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"narrow"},{"name":"activation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"narrow"},{"name":"positive regulation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"exact"},{"name":"positive regulation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"up regulation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"up regulation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"exact"},{"name":"up regulation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"up-regulation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"up-regulation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"exact"},{"name":"up-regulation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"upregulation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"upregulation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"exact"},{"name":"upregulation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"}],"termid":"GO:1902814"}


id: GO:0141207
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: lactate + ATP + L-lysyl-[protein] = N(6)-lactoyl-L-lysyl-[protein]+ AMP + diphosphate. Can also act on free lactate.","definition_xrefs":["PMID:38653238","RHEA:80271","PMID:38512451"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming phosphoric ester bonds","termid":"GO:0016886"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003674","GO:0016874","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"peptide lactyltransferase (ATP-dependent) activity","synonyms":[{"name":"peptide lactyltransferase (ATP dependent) activity","type":"exact"},{"name":"peptide lactyltransferase activity","type":"broad"}],"termid":"GO:0141207"}


id: GO:0070294
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A renal system process in which sodium ions are taken up from the collecting ducts and proximal and distal loops of the nephron. In non-mammalian species, absorption may occur in related structures.","definition_xrefs":["GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal sodium ion transport","termid":"GO:0003096"},{"relation_name":"is_a","term_name":"renal absorption","termid":"GO:0070293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"renal sodium ion absorption","synonyms":[{"name":"nephron sodium ion absorption","type":"exact"},{"name":"renal sodium ion reabsorption","type":"exact"}],"termid":"GO:0070294"}


id: GO:1990411
data:
  {"annotated_genes":["SJAG_03856"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72825],"is_not":false,"summary":null,"term":"GO:1990411"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: hercynylcysteine sulfoxide + 2H+ = ergothioneine + pyruvate + ammonium.","definition_xrefs":["PMID:24828577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03856":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"hercynylcysteine sulfoxide lyase activity (ergothioneine-forming)","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:42688","MetaCyc:RXN-14428"],"termid":"GO:1990411","terms_by_termid":{"GO:1990411":null}}


id: PBO:0005035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMR domain protein, possibly involved in DNA repair","termid":"PBO:0005035"}


id: GO:0003417
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the cartilage that will provide a scaffold for mineralization of endochondral bones as they elongate or grow.","definition_xrefs":["GOC:dph","GOC:ascb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cartilage development involved in endochondral bone morphogenesis","termid":"GO:0060351"},{"relation_name":"is_a","term_name":"connective tissue development","termid":"GO:0061448"},{"relation_name":"part_of","term_name":"endochondral bone growth","termid":"GO:0003416"}],"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":"growth plate cartilage development","termid":"GO:0003417"}


id: PBO:0073241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenophosphate synthetase 1 pseudogene 6","termid":"PBO:0073241"}


id: PBO:0088487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA translocase/ SUMO-targeted ubiquitin ligase E3","termid":"PBO:0088487"}


id: GO:0004029
data:
  {"annotated_genes":["SJAG_00482","SJAG_03786","SJAG_02961"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77937,80488],"is_not":false,"summary":null,"term":"GO:0004029"},{"annotations":[102826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140087"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: an aldehyde + H2O + NAD+ = a carboxylate + 2 H+ + NADH.","definition_xrefs":["RHEA:16185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde dehydrogenase [NAD(P)+] activity","termid":"GO:0004030"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00482":null,"SJAG_02961":null,"SJAG_03786":null},"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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"aldehyde dehydrogenase (NAD+) activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-71723","Reactome:R-HSA-6808496","Reactome:R-HSA-6808487","Reactome:R-HSA-5696091","MetaCyc:ALDHDEHYDROG-RXN","Reactome:R-HSA-6813749","UM-BBD_reactionID:r0605","Reactome:R-HSA-5692261","Reactome:R-HSA-389609","EC:1.2.1.3","UM-BBD_reactionID:r0023","Reactome:R-HSA-71691","UM-BBD_reactionID:r0003","Wikipedia:Aldehyde_dehydrogenase_(NAD+)","Reactome:R-HSA-380608"],"synonyms":[{"name":"CoA-independent aldehyde dehydrogenase activity","type":"related"},{"name":"NAD-aldehyde dehydrogenase activity","type":"related"},{"name":"NAD-dependent 4-hydroxynonenal dehydrogenase activity","type":"related"},{"name":"NAD-dependent aldehyde dehydrogenase activity","type":"related"},{"name":"NAD-linked aldehyde dehydrogenase activity","type":"related"},{"name":"aldehyde dehydrogenase (NAD+)","type":"related"},{"name":"aldehyde:NAD+ oxidoreductase activity","type":"related"},{"name":"m-methylbenzaldehyde dehydrogenase activity","type":"related"},{"name":"propionaldehyde dehydrogenase activity","type":"related"}],"termid":"GO:0004029","terms_by_termid":{"GO:0004029":null,"GO:0140087":null}}


id: PBO:0066015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor activity modifying protein 2","termid":"PBO:0066015"}


id: PBO:0065993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid induced 2","termid":"PBO:0065993"}


id: GO:0070718
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the platelet-derived growth factor alpha receptor (alphaPDGFR; PDGFRA) and the adaptor protein SHP-2, and is involved signaling via the PDGFR signaling pathway.","definition_xrefs":["GOC:mah","PMID:8943348"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"alphaPDGFR-SHP-2 complex","synonyms":[{"name":"PDGFRA-SHP-2 complex, PDGF stimulated","type":"narrow"}],"termid":"GO:0070718"}


id: GO:1904583
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a polyamine macromolecule stimulus.","definition_xrefs":["PMID:20805360","GO_REF:0000071","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to polyamine macromolecule","synonyms":[{"name":"response to polyamine","type":"exact"},{"name":"response to polyamines","type":"exact"}],"termid":"GO:1904583"}


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


id: FYPO:0005739
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid segregation results in the division of chromosomes into two distinct unequal masses containing unseparated sister chromatids, located at or near the ends of an elongated mitotic spindle.","definition_xrefs":["PomBase:mah","PMID:11792803","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complete but unequal mitotic sister chromatid segregation","termid":"FYPO:0001270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000641","FYPO:0005447","FYPO:0000337","FYPO:0001320","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"complete but unequal mitotic sister chromatid segregation with unseparated chromosomes","termid":"FYPO:0005739"}


id: MONDO:0011517
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypertension due to gain-of-function mutations in the mineralocorticoid receptor is a rare genetic hypertension characterized by a familial severe hypertension with an onset before age 20 years, associated with suppressed plasma renin and low aldosterone levels in the presence of low or normal levels of the mineralocorticoid aldosterone, that is highly resistant to antihypertensive medication. During pregnancy, there is a marked exacerbation of hypertension, accompanied by low serum potassium levels and undetectable aldosterone levels, but without signs of preeclampsia, requiring early delivery.","definition_xrefs":["Orphanet:88660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"pregnancy disorder","termid":"MONDO:0024575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudohyperaldosteronism type 2","secondary_identifiers":["icd11.foundation:538048714","UMLS:C1854631","GARD:19093","MEDGEN:343170","MESH:C565359","SCTID:766937004","OMIM:605115"],"synonyms":[{"name":"early-onset hypertension with exacerbation in pregnancy","type":"exact"},{"name":"hypertension due to gain-of-function mutations in the mineralocorticoid receptor","type":"exact"},{"name":"hypertension, early-onset, autosomal dominant, with Severe exacerbation in pregnancy","type":"related"},{"name":"hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy","type":"exact"},{"name":"hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy","type":"related"}],"termid":"MONDO:0011517","xrefs":{"Monarch":{"xref_id":"0011517"}}}


id: PBO:0071688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L37 pseudogene 20","termid":"PBO:0071688"}


id: PBO:0049209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate ionotropic receptor NMDA type subunit 2C","termid":"PBO:0049209"}


id: GO:1903091
data:
  {"annotated_genes":["SJAG_03652","SJAG_02152","SJAG_03808","SJAG_02962"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92086,92087,119473,120771],"is_not":false,"summary":null,"term":"GO:1903091"}]},"cv_name":"biological_process","definition":"The process in which pyridoxamine is transported across a membrane.","definition_xrefs":["GO_REF:0000069","GOC:TermGenie","PMID:15701794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyridoxamine transport","termid":"GO:0031922"},{"relation_name":"is_a","term_name":"vitamin transmembrane transport","termid":"GO:0035461"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02152":null,"SJAG_02962":null,"SJAG_03652":null,"SJAG_03808":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"pyridoxamine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1903091","terms_by_termid":{"GO:1903091":null}}


id: PBO:0044596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDB1 and CUL4 associated factor 4 like 2","termid":"PBO:0044596"}


id: MONDO:0018353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Refractory celiac disease (RCD) is a complex autoimmune disorder much like the more common celiac disease but, unlike celiac disease, it is resistant or unresponsive to at least 12 months of treatment with a strict gluten-free diet. Gliadin, a component of the wheat storage protein gluten, together with similar proteins in barley and rye, are the villains that trigger the immune reaction in celiac disease. The diagnosis of RCD is made by exclusion, especially of any other disorder that can affect the huge number of thread-like projections that line the interior of the intestine (intestinal villi), such as intestinal lymphoma, Crohn's disease, small intestinal bacterial overgrowth or hypogammaglobulinemia.","direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"refractory celiac disease","secondary_identifiers":["EFO:0009266","GARD:21640","ICD10CM:K90.0","UMLS:C4749333","MEDGEN:1670595","NORD:1653","Orphanet:398063"],"synonyms":[{"name":"intractable celiac sprue","type":"exact"},{"name":"intractable coeliac sprue","type":"exact"},{"name":"refractory CD","type":"exact"},{"name":"refractory sprue","type":"exact"},{"name":"type I refractory sprue","type":"narrow"},{"name":"type II refractory sprue","type":"narrow"}],"termid":"MONDO:0018353","xrefs":{"Monarch":{"xref_id":"0018353"}}}


id: MONDO:0003791
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A male urethral cancer that involves the prostatic urethra.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male urethral cancer","termid":"MONDO:0004197"}],"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":"prostatic urethral cancer","secondary_identifiers":["MEDGEN:308065","NCIT:C39870","DOID:6167","UMLS:C1514523"],"synonyms":[{"name":"male urethral cancer of prostatic urethra","type":"exact"},{"name":"prostatic urethra male urethral cancer","type":"exact"},{"name":"prostatic urethral malignant neoplasm","type":"exact"}],"termid":"MONDO:0003791","xrefs":{"Monarch":{"xref_id":"0003791"}}}


id: PBO:0063961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-4-phosphate 5-kinase type 1 pseudogene 2","termid":"PBO:0063961"}


id: GO:0034400
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A plastid found in senescing, formerly green tissues that is derived from a chloroplast that undergoes an organized developmental program of senescence.","definition_xrefs":["PMID:24668747","PMID:12654863"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid","termid":"GO:0009536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"gerontoplast","termid":"GO:0034400"}


id: GO:0030042
data:
  {"annotated_genes":["SJAG_00279","SJAG_03380","SJAG_01993","SJAG_02700","SJAG_01894","SJAG_03025"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71999,75262],"is_not":false,"summary":null,"term":"GO:0030042"},{"annotations":[94272,82069,81020,77432],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0051016"}]},"cv_name":"biological_process","definition":"Disassembly of actin filaments by the removal of actin monomers from a filament.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin polymerization or depolymerization","termid":"GO:0008154"},{"relation_name":"is_a","term_name":"protein depolymerization","termid":"GO:0051261"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00279":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02700":null,"SJAG_03025":null,"SJAG_03380":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0030036","GO:0007010","GO:0008150"],"is_obsolete":false,"name":"actin filament depolymerization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"actin depolymerization","type":"exact"},{"name":"actin depolymerizing activity","type":"related"}],"termid":"GO:0030042","terms_by_termid":{"GO:0030042":null,"GO:0051016":null}}


id: PBO:0027933
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H3-K9_dimethylation_at_centromere","termid":"PBO:0027933"}


id: GO:0031092
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding the platelet alpha granule.","definition_xrefs":["PMID:8467233","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule membrane","termid":"GO:0030667"},{"relation_name":"part_of","term_name":"platelet alpha granule","termid":"GO:0031091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"platelet alpha granule membrane","synonyms":[{"name":"platelet alpha-granule membrane","type":"exact"}],"termid":"GO:0031092"}


id: _global:has_functional_parent
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"'Entity A' has_functional_parent 'Entity B' implies that 'Entity B' has at least one chacteristic group from which 'Entity A' can be derived by functional modification.","definition_xrefs":["PubMed:18688235"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_functional_parent","termid":"_global:has_functional_parent"}


id: MONDO:1010509
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cerebral amyloid angiopathy that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral amyloid angiopathy, non-human animal","termid":"MONDO:1010028"},{"relation_name":"is_a","term_name":"amyloidosis, domestic cat","termid":"MONDO:1011468"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral amyloid angiopathy, domestic cat","secondary_identifiers":["OMIA:002138-9685"],"termid":"MONDO:1010509","xrefs":{"Monarch":{"xref_id":"1010509"}}}


id: PBO:0055158
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 2577","termid":"PBO:0055158"}


id: GO:0035742
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of an activated CD8-positive, alpha-beta T cell population by cell division.","definition_xrefs":["GOC:BHF","CL:0000906"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CD8-positive, alpha-beta T cell proliferation","termid":"GO:0035740"}],"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":"activated CD8-positive, alpha-beta T cell proliferation","termid":"GO:0035742"}


id: MONDO:0034671
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-syndromic complex polydactyly (obsolete MONDO:0034671)","secondary_identifiers":["Orphanet:498470"],"termid":"MONDO:0034671","xrefs":{"Monarch":{"xref_id":"0034671"}}}


id: PBO:0082683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the ESCRT-II complex; ESCRT-II is involved in ubiquitin-dependent sorting of proteins into the endosome; appears to be functionally related to SNF7; involved in glucose derepression","termid":"PBO:0082683"}


id: MONDO:0022394
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dysplasia of cervix","termid":"MONDO:0006736"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical intraepithelial neoplasia","secondary_identifiers":["SCTID:285636001","NCIT:C3782","UMLS:C0206708","GARD:9244","MEDGEN:60214"],"synonyms":[{"name":"Cervical Dysplasia","type":"related"},{"name":"Cervical Intraepithelial Neoplasia","type":"related"},{"name":"Cervical Intraepithelial Neoplasm","type":"related"},{"name":"Cervical Intraepithelial Neoplasms","type":"related"},{"name":"Cervical intraepithelial neoplasia","type":"related"},{"name":"Cervix Intraepithelial Neoplasia","type":"related"},{"name":"Cervix Uteri Intraepithelial Neoplasia","type":"related"},{"name":"Intraepithelial Neoplasia of Cervix","type":"related"},{"name":"Intraepithelial Neoplasia of Cervix Uteri","type":"related"},{"name":"Intraepithelial Neoplasia of Uterine Cervix","type":"related"},{"name":"Intraepithelial Neoplasia of the Cervix","type":"related"},{"name":"Intraepithelial Neoplasia of the Cervix Uteri","type":"related"},{"name":"Intraepithelial Neoplasia of the Uterine Cervix","type":"related"},{"name":"Intraepithelial Neoplasia, Cervical","type":"related"},{"name":"Intraepithelial Neoplasm, Cervical","type":"related"},{"name":"Intraepithelial Neoplasms, Cervical","type":"related"},{"name":"NEOPL CERVICAL INTRAEPITHELIAL","type":"related"},{"name":"Neoplasia, Cervical Intraepithelial","type":"related"},{"name":"Neoplasm, Cervical Intraepithelial","type":"related"},{"name":"Neoplasms, Cervical Intraepithelial","type":"related"},{"name":"Uterine Cervix Intraepithelial Neoplasia","type":"related"}],"termid":"MONDO:0022394","xrefs":{"Monarch":{"xref_id":"0022394"}}}


id: PBO:0046824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid binding protein 3","termid":"PBO:0046824"}


id: GO:0030811
data:
  {"annotated_genes":["SJAG_05314","SJAG_00685","SJAG_02785"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78030,74975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"},{"annotations":[71907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006110"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of nucleotides.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nucleotide metabolic process","termid":"GO:0006140"},{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"},{"relation_name":"regulates","term_name":"nucleotide catabolic process","termid":"GO:0009166"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_02785":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"regulation of nucleotide catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"regulation of nucleotide breakdown","type":"exact"},{"name":"regulation of nucleotide catabolism","type":"exact"},{"name":"regulation of nucleotide degradation","type":"exact"}],"termid":"GO:0030811","terms_by_termid":{"GO:0006110":null,"GO:0045820":null}}


id: PBO:0056274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAN1B1 divergent transcript","termid":"PBO:0056274"}


id: SO:0001966
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A modified DNA cytosine base feature, modified by a carboxy group at the 5 carbon.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytosine","termid":"SO:0001963"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5_carboxylcytosine","secondary_identifiers":["http:http\\://www.pacificbiosciences.com/pdf/WP_Detecting_DNA_Base_Modifications_Using_SMRT_Sequencing.pdf"],"synonyms":[{"name":"5-caC","type":"exact"},{"name":"5-carboxycytosine","type":"exact"}],"termid":"SO:0001966"}


id: MONDO:0013420
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 CX3CR1 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 12","secondary_identifiers":["DOID:0110024","OMIM:613784","MEDGEN:462429","UMLS:C3151079"],"synonyms":[{"name":"ARMD12","type":"exact"},{"name":"CX3CR1 age-related macular degeneration","type":"exact"},{"name":"age related macular degeneration type 12","type":"exact"},{"name":"age-related macular degeneration caused by mutation in CX3CR1","type":"exact"},{"name":"macular Degeneration, age-related, type 12","type":"exact"},{"name":"macular degeneration, age-related, 12","type":"related"}],"termid":"MONDO:0013420","xrefs":{"Monarch":{"xref_id":"0013420"}}}


id: GO:0045157
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the directed movement of electrons within the noncyclic electron transport pathway of photosynthesis.","definition_xrefs":["GOC:ai","ISBN:0716731363"],"gene_count":0,"genotype_count":0,"name":"obsolete electron transporter, transferring electrons within the noncyclic electron transport pathway of photosynthesis activity (obsolete GO:0045157)","termid":"GO:0045157"}


id: PBO:0109358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LAMTOR5 and SLC16A4 antisense RNA 1","termid":"PBO:0109358"}


id: GO:0002638
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of immunoglobulin production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of immunoglobulin production","termid":"GO:0002637"},{"relation_name":"is_a","term_name":"negative regulation of production of molecular mediator of immune response","termid":"GO:0002701"},{"relation_name":"negatively_regulates","term_name":"immunoglobulin production","termid":"GO:0002377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of immunoglobulin production","secondary_identifiers":["GO:0002641","GO:0051025"],"synonyms":[{"name":"down regulation of immunoglobulin production","type":"exact"},{"name":"down-regulation of immunoglobulin production","type":"exact"},{"name":"downregulation of immunoglobulin production","type":"exact"},{"name":"inhibition of immunoglobulin production","type":"narrow"},{"name":"negative regulation of immunoglobulin biosynthetic process","type":"narrow"},{"name":"negative regulation of immunoglobulin secretion","type":"narrow"}],"termid":"GO:0002638"}


id: MONDO:0007847
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":"keloid formation","secondary_identifiers":["UMLS:C3149494","OMIM:148100","MEDGEN:460844"],"synonyms":[{"name":"keloid formation","type":"exact"}],"termid":"MONDO:0007847","xrefs":{"Monarch":{"xref_id":"0007847"}}}


id: PBO:0028757
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_mitotic_G1_phase_entry_during_cellular_response_to_ionizing_radiation","termid":"PBO:0028757"}


id: PBO:0034410
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_acquisition_of_features_of","termid":"PBO:0034410"}


id: MONDO:0017234
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of prion disease that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary dementia","termid":"MONDO:0015547"},{"relation_name":"excluded_subClassOf","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"genotype_count":0,"name":"obsolete inherited prion disease (obsolete MONDO:0017234)","secondary_identifiers":["NANDO:1200188","Orphanet:280400"],"synonyms":[{"name":"familial prion disease","type":"exact"},{"name":"hereditary prion disease","type":"exact"}],"termid":"MONDO:0017234","xrefs":{"Monarch":{"xref_id":"0017234"}}}


id: MONDO:0800397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited retinopathy caused by bi-allelic variants in the GRM6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"GRM6-related retinopathy","termid":"MONDO:0800397","xrefs":{"Monarch":{"xref_id":"0800397"}}}


id: MONDO:0006098
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lobular neoplasia characterized by lobular epithelial proliferation that does not completely fill the lobular unit of the breast.","definition_xrefs":["NCIT:C4730"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system cancer","termid":"MONDO:0000653"},{"relation_name":"is_a","term_name":"lobular neoplasia","termid":"MONDO:0002486"},{"relation_name":"is_a","term_name":"hyperplasia","termid":"MONDO:0005043"}],"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":"atypical lobular breast hyperplasia","secondary_identifiers":["EFO:1000100","MEDGEN:277968","ICD9:610.8","SCTID:450697004","UMLS:C1368920"],"synonyms":[{"name":"ALH","type":"exact"},{"name":"atypical breast lobular hyperplasia","type":"exact"},{"name":"atypical lobular breast hyperplasia","type":"exact"},{"name":"atypical lobular hyperplasia","type":"exact"},{"name":"atypical lobular hyperplasia of breast","type":"exact"},{"name":"atypical lobular hyperplasia of the breast","type":"exact"}],"termid":"MONDO:0006098","xrefs":{"Monarch":{"xref_id":"0006098"}}}


id: GO:0051984
data:
  {"annotated_genes":["SJAG_03681","SJAG_03126","SJAG_02169","SJAG_04597","SJAG_03048","SJAG_04259","SJAG_01837","SJAG_01679","SJAG_00082","SJAG_01297","SJAG_04280","SJAG_02451","SJAG_00883","SJAG_03353","SJAG_02336","SJAG_01805","SJAG_04140","SJAG_05290"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116267,115780,113954,117899,110230,92668,101540,105846,109202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[96146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[107146,118007,113955],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902425"},{"annotations":[113194,95755,118678,104336,91948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140429"},{"annotations":[91949,96361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902846"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chromosome segregation, the process in which genetic material, in the form of chromosomes, is organized and then physically separated and apportioned to two or more sets.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chromosome segregation","termid":"GO:0051983"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"positively_regulates","term_name":"chromosome segregation","termid":"GO:0007059"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00883":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04140":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04597":null,"SJAG_05290":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"positive regulation of chromosome segregation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of chromosome segregation","type":"narrow"},{"name":"stimulation of chromosome segregation","type":"narrow"},{"name":"up regulation of chromosome segregation","type":"exact"},{"name":"up-regulation of chromosome segregation","type":"exact"},{"name":"upregulation of chromosome segregation","type":"exact"}],"termid":"GO:0051984","terms_by_termid":{"GO:0140429":null,"GO:0140499":null,"GO:1902425":null,"GO:1902426":null,"GO:1902846":null}}


id: GO:0036212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which the contractile ring is maintained, typically in response to an internal or external cue.","definition_xrefs":["GOC:vw","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete contractile ring maintenance (obsolete GO:0036212)","termid":"GO:0036212"}


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


id: PBO:0072939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small Cajal body-specific RNA 18B","termid":"PBO:0072939"}


id: GO:0140430
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of a chromosome passenger complex localization to kinetochore.","definition_xrefs":["PMID:20739936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein localization to kinetochore","termid":"GO:1905342"},{"relation_name":"positively_regulates","term_name":"chromosome passenger complex localization to kinetochore","termid":"GO:0072356"}],"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 chromosome passenger complex localization to kinetochore","termid":"GO:0140430"}


id: GO:0050322
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: taurine + 2-oxoglutarate = sulfoacetaldehyde + L-glutamate.","definition_xrefs":["RHEA:16353","PMID:16535664"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016769","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"taurine-2-oxoglutarate transaminase activity","secondary_identifiers":["EC:2.6.1.55","MetaCyc:RXN-2301"],"synonyms":[{"name":"taurine aminotransferase activity","type":"exact"},{"name":"taurine transaminase activity","type":"exact"},{"name":"taurine--alpha-ketoglutarate aminotransferase activity","type":"related"},{"name":"taurine--glutamate transaminase activity","type":"related"},{"name":"taurine:2-oxoglutarate aminotransferase activity","type":"related"}],"termid":"GO:0050322"}


id: PR:O43026
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gpd3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde-3-phosphate dehydrogenase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC354.12","synonyms":[{"name":"GAPDH 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gpd3","type":"exact"}],"termid":"PR:O43026"}


id: PBO:0077321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 59 like","termid":"PBO:0077321"}


id: PBO:0085072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-proteolytic ATPase of the AAA family; stimulates incorporation of the pyridoxal phosphate cofactor into Hem1p (5-aminolevulinic acid synthase); localized to the mitochondrial matrix; ortholog of vertebrate CLPX, which promotes erythropoiesis","termid":"PBO:0085072"}


id: GO:1904725
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any TFIIB-class transcription factor binding that is involved in negative regulation of DNA-templated transcription.","definition_xrefs":["PMID:12461786","GOC:rb","GOC:TermGenie","GO_REF:0000061"],"gene_count":0,"genotype_count":0,"name":"obsolete TFIIB-class transcription factor binding involved in negative regulation of transcription (obsolete GO:1904725)","synonyms":[{"name":"TFIIB-class transcription factor binding involved in down regulation of gene-specific transcription","type":"related"},{"name":"TFIIB-class transcription factor binding involved in down regulation of transcription, DNA-dependent","type":"exact"},{"name":"TFIIB-class transcription factor binding involved in down-regulation of gene-specific transcription","type":"related"},{"name":"TFIIB-class transcription factor binding involved in down-regulation of transcription, DNA-dependent","type":"exact"},{"name":"TFIIB-class transcription factor binding involved in downregulation of gene-specific transcription","type":"related"},{"name":"TFIIB-class transcription factor binding involved in downregulation of transcription, DNA-dependent","type":"exact"},{"name":"TFIIB-class transcription factor binding involved in inhibition of gene-specific transcription","type":"related"},{"name":"TFIIB-class transcription factor binding involved in inhibition of transcription, DNA-dependent","type":"narrow"},{"name":"TFIIB-class transcription factor binding involved in negative regulation of cellular transcription, DNA-dependent","type":"exact"},{"name":"TFIIB-class transcription factor binding involved in negative regulation of gene-specific transcription","type":"related"},{"name":"TFIIB-class transcription factor binding involved in negative regulation of transcription, DNA-dependent","type":"exact"},{"name":"TFIIB-class transcription factor binding involved in negative regulation of transcription, DNA-templated","type":"exact"},{"name":"TFIIB-class transcription factor binding involved in transcription repressor activity","type":"related"}],"termid":"GO:1904725"}


id: PBO:0041087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain and PHD finger containing 3","termid":"PBO:0041087"}


id: GO:0003986
data:
  {"annotated_genes":["SJAG_02985","SJAG_02769"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77333,78673],"is_not":false,"summary":null,"term":"GO:0003986"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + H2O = acetate + CoA + H+.","definition_xrefs":["EC:3.1.2.1","RHEA:20289"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA hydrolase activity","termid":"GO:0016289"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02769":null,"SJAG_02985":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0016788","GO:0003824"],"is_obsolete":false,"name":"acetyl-CoA hydrolase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-2066779","Reactome:R-HSA-390304","MetaCyc:ACETYL-COA-HYDROLASE-RXN","KEGG_REACTION:R00227"],"synonyms":[{"name":"acetyl-CoA deacylase activity","type":"related"},{"name":"acetyl-CoA thiol esterase activity","type":"related"},{"name":"acetyl coenzyme A acylase activity","type":"related"},{"name":"acetyl coenzyme A deacylase activity","type":"related"},{"name":"acetyl coenzyme A hydrolase activity","type":"related"},{"name":"acetyl-CoA acylase activity","type":"related"}],"termid":"GO:0003986","terms_by_termid":{"GO:0003986":null}}


id: MONDO:0011729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stroke, susceptibility to, 1","secondary_identifiers":["MEDGEN:335696","UMLS:C1847482","OMIM:606799"],"synonyms":[{"name":"Strk1","type":"related"},{"name":"stroke, susceptibility to, 1","type":"exact"},{"name":"stroke, susceptibility to, type 1","type":"exact"}],"termid":"MONDO:0011729","xrefs":{"Monarch":{"xref_id":"0011729"}}}


id: GO:1903632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of aminoacyl-tRNA ligase activity.","definition_xrefs":["GO_REF:0000059","PMID:2280766","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of aminoacyl-tRNA ligase activity (obsolete GO:1903632)","synonyms":[{"name":"activation of aminoacyl-tRNA ligase activity","type":"narrow"},{"name":"activation of aminoacyl-tRNA synthetase activity","type":"narrow"},{"name":"activation of aminoacyl-tRNA synthetase auxiliary protein activity","type":"related"},{"name":"positive regulation of aminoacyl-tRNA synthetase activity","type":"exact"},{"name":"positive regulation of aminoacyl-tRNA synthetase auxiliary protein activity","type":"related"},{"name":"up regulation of aminoacyl-tRNA ligase activity","type":"exact"},{"name":"up regulation of aminoacyl-tRNA synthetase activity","type":"exact"},{"name":"up regulation of aminoacyl-tRNA synthetase auxiliary protein activity","type":"related"},{"name":"up-regulation of aminoacyl-tRNA ligase activity","type":"exact"},{"name":"up-regulation of aminoacyl-tRNA synthetase activity","type":"exact"},{"name":"up-regulation of aminoacyl-tRNA synthetase auxiliary protein activity","type":"related"},{"name":"upregulation of aminoacyl-tRNA ligase activity","type":"exact"},{"name":"upregulation of aminoacyl-tRNA synthetase activity","type":"exact"},{"name":"upregulation of aminoacyl-tRNA synthetase auxiliary protein activity","type":"related"}],"termid":"GO:1903632"}


id: PBO:0057867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3178","termid":"PBO:0057867"}


id: PBO:0002219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA repair protein Rad50","termid":"PBO:0002219"}


id: PBO:0005746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfonate dioxygenase (predicted)","termid":"PBO:0005746"}


id: MONDO:0002720
data:
  {"annotated_genes":["SJAG_03429"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm that occurs in sella turcica. Representative examples include craniopharyngioma and pituitary gland adenoma.","definition_xrefs":["NCIT:C4944"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skull base neoplasm","termid":"MONDO:0002785"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03429":null},"genotype_count":0,"is_obsolete":false,"name":"sella turcica neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ONCOTREE:SELT","DOID:3643","MEDGEN:148188","UMLS:C0748616"],"synonyms":[{"name":"neoplasm of sella turcica","type":"exact"},{"name":"neoplasm of the sella turcica","type":"exact"},{"name":"sella turcica neoplasm","type":"exact"},{"name":"sella turcica tumor","type":"exact"},{"name":"sella turcica tumour","type":"exact"},{"name":"sellar neoplasm","type":"exact"},{"name":"sellar tumor","type":"exact"},{"name":"sellar tumour","type":"exact"},{"name":"selt","type":"related"},{"name":"tumor of sella turcica","type":"exact"},{"name":"tumor of the sella turcica","type":"exact"},{"name":"tumour of sella turcica","type":"exact"},{"name":"tumour of the sella turcica","type":"exact"}],"termid":"MONDO:0002720","terms_by_termid":{"MONDO:0009050":null},"xrefs":{"Monarch":{"xref_id":"0002720"}}}


id: MOD:01009
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"},{"relation_name":"is_a","term_name":"didehydrogenated residue","termid":"MOD:01888"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenated proline","termid":"MOD:01009"}


id: GO:0036296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus reflecting an increase in the level of oxygen.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxygen levels","termid":"GO:0070482"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to increased oxygen levels","synonyms":[{"name":"response to raised oxygen levels","type":"exact"}],"termid":"GO:0036296"}


id: PBO:0077178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toll like receptor 2","termid":"PBO:0077178"}


id: PBO:0072573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonucleotide reductase regulatory TP53 inducible subunit M2B","termid":"PBO:0072573"}


id: GO:0018592
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-nitrocatechol + NAD(P)H + O2 = 2-hydroxy-1,4-benzoquinone + nitrite + NAD(P)+ + H2O.","definition_xrefs":["EC:1.14.13.166"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"4-nitrocatechol 4-monooxygenase activity","secondary_identifiers":["UM-BBD_reactionID:r0231"],"termid":"GO:0018592"}


id: PBO:0027290
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_glutathione_peroxidase_activity","termid":"PBO:0027290"}


id: PBO:0080892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YTH N6-methyladenosine RNA binding protein F2","termid":"PBO:0080892"}


id: PR:O60055
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A small subunit processome component 20 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03996","PANTHER:PTHR17695:SF11","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":"U3 small nucleolar RNA-associated protein 20 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC56F2.04","secondary_identifiers":["UniProtKB:O60055"],"synonyms":[{"name":"Spom972h-UTP20","type":"exact"},{"name":"U3 snoRNA-associated protein 20 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60055"}


id: MONDO:0019608
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete 46,XX disorder of sex development induced by maternal-derived androgen (obsolete MONDO:0019608)","secondary_identifiers":["Orphanet:91144","icd11.foundation:293874628"],"synonyms":[{"name":"46,XX DSD induced by maternal-derived androgen","type":"exact"}],"termid":"MONDO:0019608","xrefs":{"Monarch":{"xref_id":"0019608"}}}


id: MONDO:0032862
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":"hydrocephalus, congenital communicating, 1","secondary_identifiers":["MEDGEN:1684770","OMIM:618667","GARD:18090","UMLS:C5231454"],"synonyms":[{"name":"HYDCC1","type":"related"},{"name":"HYDROCEPHALUS, CONGENITAL COMMUNICATING, 1","type":"related"}],"termid":"MONDO:0032862","xrefs":{"Monarch":{"xref_id":"0032862"}}}


id: GO:0033379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protease is maintained in a secretory granule in a T cell and prevented from moving elsewhere.","definition_xrefs":["GOC:tb","GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of protein location in T cell secretory granule","termid":"GO:0033377"},{"relation_name":"part_of","term_name":"protease localization to T cell secretory granule","termid":"GO:0033375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"maintenance of protease location in T cell secretory granule","synonyms":[{"name":"maintenance of protease localization in T cell secretory granule","type":"related"},{"name":"maintenance of protease localization in T lymphocyte secretory granule","type":"exact"},{"name":"maintenance of protease localization in T-cell secretory granule","type":"exact"},{"name":"maintenance of protease localization in T-lymphocyte secretory granule","type":"exact"}],"termid":"GO:0033379"}


id: MONDO:0012222
data:
  {"annotated_genes":["SJAG_02949"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87091],"is_not":false,"summary":null,"term":"MONDO:0012222"}]},"cv_name":"mondo","definition":"Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 2 is a very rare mild adult type of NAGA deficiency with the features of angiokeratoma corporis diffusum and mild sensory neuropathy.","definition_xrefs":["Orphanet:79280"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-N-acetylgalactosaminidase deficiency","termid":"MONDO:0017779"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02949":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0002561","MONDO:0005066"],"is_obsolete":false,"name":"alpha-N-acetylgalactosaminidase deficiency type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:609242","GARD:9161","DOID:0112319","icd11.foundation:266505438","NANDO:1200136","SCTID:880065001","UMLS:C1836522","MEDGEN:324539"],"synonyms":[{"name":"Alpha-N-acetylgalactosaminidase deficiency adult onset","type":"related"},{"name":"Alpha-N-acetylgalactosaminidase deficiency, adult-onset","type":"related"},{"name":"Alpha-N-acetylgalactosaminidase deficiency, type 2","type":"related"},{"name":"KANZAKI disease","type":"related"},{"name":"Kanzaki disease","type":"exact"},{"name":"NAGA deficiency type 2","type":"exact"},{"name":"Naga deficiency, type 2","type":"related"},{"name":"Schindler disease type 2","type":"exact"},{"name":"Schindler disease, type 2","type":"related"},{"name":"adult-onset Alpha-N-acetylgalactosaminidase deficiency","type":"exact"}],"termid":"MONDO:0012222","terms_by_termid":{"MONDO:0012222":null},"xrefs":{"Monarch":{"xref_id":"0012222"}}}


id: GO:0034885
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gamma-N-formylaminovinylacetate + H2O = gamma-aminovinylacetate + HCOOH.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete gamma-N-formylaminovinylacetate hydrolase activity (obsolete GO:0034885)","termid":"GO:0034885"}


id: MONDO:0005173
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A precancerous lesion of the skin composed of atypical keratinocytes. It is characterized by the presence of thick, scaly patches of skin. Several histologic variants have been described, including atrophic, acantholytic, and hyperkeratotic variants.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pre-malignant neoplasm","termid":"MONDO:0000611"},{"relation_name":"is_a","term_name":"skin neoplasm","termid":"MONDO:0002531"}],"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":"actinic keratosis","secondary_identifiers":["ICD10CM:L57.0","ICD9:702.0","HP:0025127","DOID:8866","SCTID:201101007","SCTID:46795000","UMLS:C0022602","icd11.foundation:1803982621","EFO:0002496","MESH:D055623","NCIT:C3148","MEDGEN:9627","ICD9:702.19"],"synonyms":[{"name":"SK - solar keratosis","type":"exact"},{"name":"Senile hyperkeratosis","type":"related"},{"name":"Senile keratosis","type":"related"},{"name":"actinic (solar) keratosis","type":"exact"},{"name":"actinic keratosis","type":"exact"},{"name":"actinic keratosis (disease)","type":"exact"},{"name":"senile keratosis","type":"related"},{"name":"solar keratosis","type":"exact"}],"termid":"MONDO:0005173","xrefs":{"Monarch":{"xref_id":"0005173"}}}


id: PBO:0030449
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_phosphatase_activity","termid":"PBO:0030449"}


id: GO:0042736
data:
  {"annotated_genes":["SJAG_01566","SJAG_01582","SJAG_03946"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[93874,98412,99423],"is_not":false,"summary":null,"term":"GO:0042736"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + NADH = ADP + 2 H+ + NADPH.","definition_xrefs":["RHEA:12260","EC:2.7.1.86"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01566":null,"SJAG_01582":null,"SJAG_03946":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"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016301","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"NADH kinase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:NADH-KINASE-RXN","KEGG_REACTION:R00105"],"synonyms":[{"name":"ATP:NADH 2'-phosphotransferase activity","type":"related"},{"name":"DPNH kinase activity","type":"related"},{"name":"reduced diphosphopyridine nucleotide kinase activity","type":"related"},{"name":"reduced nicotinamide adenine dinucleotide kinase (phosphorylating)","type":"related"}],"termid":"GO:0042736","terms_by_termid":{"GO:0042736":null}}


id: GO:0072085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the connecting tubule of the kidney nephron acquires its identity.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of nephron tubule identity","termid":"GO:0072081"},{"relation_name":"part_of","term_name":"connecting tubule development","termid":"GO:0072027"}],"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":"specification of connecting tubule identity","termid":"GO:0072085"}


id: GO:0034640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a mitochondrion by attachment to a microtubule, followed by elongation of the microtubule by tubulin polymerization.","definition_xrefs":["PMID:12972644","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of mitochondrion localization, microtubule-mediated","termid":"GO:0034643"},{"relation_name":"is_a","term_name":"microtubule polymerization based movement","termid":"GO:0099098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"establishment of mitochondrion localization by microtubule attachment","synonyms":[{"name":"establishment of mitochondrion localisation by microtubule attachment","type":"exact"},{"name":"mitochondrial localization by microtubule attachment","type":"exact"},{"name":"mitochondrial migration by microtubule attachment","type":"exact"},{"name":"mitochondrion migration by microtubule attachment","type":"exact"}],"termid":"GO:0034640"}


id: PBO:0038407
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-directly_regulates_activity_of","termid":"PBO:0038407"}


id: GO:0072311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a glomerular epithelial cell. Glomerular epithelial cells are specialized epithelial cells that form part of the glomerulus; there are two types, glomerular parietal epithelial cells and glomerular visceral epithelial cells.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell differentiation involved in kidney development","termid":"GO:0035850"},{"relation_name":"part_of","term_name":"glomerular epithelium development","termid":"GO:0072010"}],"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":"glomerular epithelial cell differentiation","termid":"GO:0072311"}


id: PBO:0064576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protection of telomeres 1","termid":"PBO:0064576"}


id: GO:0010890
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of sequestering of triglyceride. Triglyceride sequestration is the process of binding or confining any triester of glycerol such that it is separated from other components of a biological system.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid storage","termid":"GO:0010884"},{"relation_name":"is_a","term_name":"regulation of triglyceride storage","termid":"GO:0010889"},{"relation_name":"positively_regulates","term_name":"triglyceride storage","termid":"GO:0030730"}],"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 triglyceride storage","synonyms":[{"name":"positive regulation of sequestering of triacylglycerol","type":"exact"},{"name":"positive regulation of sequestering of triglyceride","type":"exact"},{"name":"positive regulation of triglyceride sequestration","type":"exact"}],"termid":"GO:0010890"}


id: PBO:0061064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sodium/potassium transporting ATPase interacting 3","termid":"PBO:0061064"}


id: GO:0090147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the directed movement of mitochondria to the correct region of the cell that contributes to the process of mitochondrial fission.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of establishment of mitochondrion localization involved in mitochondrial fission (obsolete GO:0090147)","synonyms":[{"name":"regulation of establishment of mitochondrion localisation involved in mitochondrial fission","type":"exact"},{"name":"regulation of mitochondrial localization involved in mitochondrial fission","type":"related"}],"termid":"GO:0090147"}


id: GO:0047112
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + O2 + phosphate + pyruvate = acetyl phosphate + CO2 + H2O2.","definition_xrefs":["RHEA:20848"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor","termid":"GO:0016623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"pyruvate oxidase activity","secondary_identifiers":["MetaCyc:1.2.3.3-RXN","EC:1.2.3.3","KEGG_REACTION:R00207"],"synonyms":[{"name":"phosphate-dependent pyruvate oxidase activity","type":"related"},{"name":"pyruvate:oxygen 2-oxidoreductase (phosphorylating)","type":"related"},{"name":"pyruvic oxidase activity","type":"related"}],"termid":"GO:0047112"}


id: PBO:0066841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 141","termid":"PBO:0066841"}


id: PBO:0062799
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OS9 endoplasmic reticulum lectin","termid":"PBO:0062799"}


id: FYPO:0000126
data:
  {"alleles_by_uniquename":{"SJAG_00610:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00610","name":"pck2delta","uniquename":"SJAG_00610:allele-1"},"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"},"SJAG_04551:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04551","name":"pmk1delta","uniquename":"SJAG_04551:allele-1"},"SJAG_04551:allele-2":{"allele_type":"amino_acid_insertion","description":"82-NITCIYDLDIIINPYNFNEVYIYEE-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sj(ins82-105)","uniquename":"SJAG_04551:allele-2"},"SJAG_04551:allele-3":{"allele_type":"other","description":"Pmk1 from S. pombe","gene_uniquename":"SJAG_04551","name":"Pmk1Sp","uniquename":"SJAG_04551:allele-3"},"SJAG_04551:allele-4":{"allele_type":"partial_amino_acid_deletion","description":"Pmk1 from S. pombe with deleted residues 82-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sp(delta82-105)","uniquename":"SJAG_04551:allele-4"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005152"},{"annotations":[121238,121223,121244,121249,121252],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007521"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased resistance to a chemical stimulus. Resistance to a chemical is usually measured by determining the maximum concentration of the chemical at which a population of cells grow and divide, and cells are deemed resistant to a chemical if they survive at a concentration of the chemical that does not allow wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell population growth","termid":"FYPO:0001356"},{"relation_name":"is_a","term_name":"increased resistance to chemical","termid":"FYPO:0002682"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_04551":null},"genotype_count":6,"genotypes_by_uniquename":{"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sj(ins82-105)(82-NITCIYDLDIIINPYNFNEVYIYEE-105)","display_uniquename":"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-2","expression":"Not assayed or wild type"}]}]},"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(delta82-105)(Pmk1 from S. pombe with deleted residues 82-105 Δaa)","display_uniquename":"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-4","expression":"Not assayed or wild type"}]}]},"Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(Pmk1 from S. pombe)","display_uniquename":"Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-3","expression":"Not assayed or wild type"}]}]},"pck1delta":{"display_name":"pck1delta","display_uniquename":"pck1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]}]},"pck2delta":{"display_name":"pck2delta","display_uniquename":"pck2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00610:allele-1","expression":"Null"}]}]},"pmk1delta":{"display_name":"pmk1delta","display_uniquename":"pmk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0002682","FYPO:0001985","FYPO:0000003","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"increased resistance to chemical during vegetative growth","references_by_uniquename":{"PMID:34198697":null},"single_locus_annotated_genes":["SJAG_04551","SJAG_00610","SJAG_01787"],"single_locus_genotype_uniquenames":["pck1delta","pmk1delta","Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","pck2delta"],"synonyms":[{"name":"increased resistance to chemical during mitotic cell cycle","type":"related"},{"name":"resistance to chemicals: increased during vegetative growth","type":"exact"},{"name":"resistant to chemical during vegetative growth","type":"exact"}],"termid":"FYPO:0000126","terms_by_termid":{"FYPO:0005152":null,"FYPO:0007521":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:1901854
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 5,6,7,8-tetrahydrosarcinapterin.","definition_xrefs":["GOC:yaf","UniPathway:UPA00069","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pteridine-containing compound catabolic process","termid":"GO:0042560"},{"relation_name":"is_a","term_name":"organophosphate catabolic process","termid":"GO:0046434"},{"relation_name":"is_a","term_name":"tricarboxylic acid catabolic process","termid":"GO:0072352"},{"relation_name":"is_a","term_name":"5,6,7,8-tetrahydrosarcinapterin metabolic process","termid":"GO:1901853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"5,6,7,8-tetrahydrosarcinapterin catabolic process","synonyms":[{"name":"5,6,7,8-tetrahydrosarcinapterin breakdown","type":"exact"},{"name":"5,6,7,8-tetrahydrosarcinapterin catabolism","type":"exact"},{"name":"5,6,7,8-tetrahydrosarcinapterin degradation","type":"exact"}],"termid":"GO:1901854"}


id: PBO:0055963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 75B","termid":"PBO:0055963"}


id: MONDO:0018933
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mazabraud syndrome is a rare primary bone dysplasia characterized by the association of fibrous dysplasia with intramuscular myxomas. Fibrous dysplasia (usually polyostotic, sometimes monostotic) occurs during the growth period and can be asymptomatic or can present with pain, skeletal deformities or fractures while intramuscular myxoma, associated with polyostotic fibrous dysplasia is usually multifocal, typically occurring in the vicinity of skeletal lesions, and presents in adulthood as a painless soft-tissue mass (most commonly in the thigh). Although it is a benign condition, local recurrences of myxomas after incomplete excision and malignant transformation of a fibrous dysplastic lesion into osteogenic sarcoma have been reported.","definition_xrefs":["Orphanet:57782"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"soft tissue neoplasm","termid":"MONDO:0006424"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mazabraud syndrome","secondary_identifiers":["UMLS:C3697137","GARD:18853","ICD9:733.29","icd11.foundation:1153435718","MEDGEN:784403","ICD9:215.9","SCTID:699251001"],"synonyms":[{"name":"Myxoma with fibrous dysplasia","type":"exact"}],"termid":"MONDO:0018933","xrefs":{"Monarch":{"xref_id":"0018933"}}}


id: PBO:0004991
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.11.1.6","termid":"PBO:0004991"}


id: PATO:0000296
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000296 speed value (obsolete PATO:0000296)","termid":"PATO:0000296"}


id: MONDO:0016263
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primitive neuroectodermal tumor that involves the body of uterus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primitive neuroectodermal tumor","termid":"MONDO:0005462"},{"relation_name":"is_a","term_name":"corpus uteri neoplasm","termid":"MONDO:0021254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primitive neuroectodermal tumor of the corpus uteri","secondary_identifiers":["UMLS:C4707724","GARD:20478","MEDGEN:1640822","Orphanet:213630"],"synonyms":[{"name":"body of uterus primitive neuroectodermal tumor","type":"exact"},{"name":"body of uterus primitive neuroectodermal tumour","type":"exact"},{"name":"malignant peripheral neuroectodermal tumor of the corpus uteri","type":"exact"},{"name":"malignant peripheral neuroectodermal tumour of the corpus uteri","type":"exact"},{"name":"peripheral neuroectodermal cancer of the corpus uteri","type":"exact"},{"name":"primitive neuroectodermal tumor of body of uterus","type":"exact"},{"name":"primitive neuroectodermal tumour of body of uterus","type":"exact"}],"termid":"MONDO:0016263","xrefs":{"Monarch":{"xref_id":"0016263"}}}


id: MONDO:0008110
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ocular dominance (obsolete MONDO:0008110)","secondary_identifiers":["OMIM:164190"],"synonyms":[{"name":"ocular dominance","type":"exact"}],"termid":"MONDO:0008110","xrefs":{"Monarch":{"xref_id":"0008110"}}}


id: MONDO:0014724
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the TCTN2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome 24","secondary_identifiers":["OMIM:616654","UMLS:C4084841","MEDGEN:905319","GARD:16150","DOID:0110993"],"synonyms":[{"name":"JBTS24","type":"exact"},{"name":"Joubert syndrome 24","type":"exact"},{"name":"Joubert syndrome caused by mutation in TCTN2","type":"exact"},{"name":"Joubert syndrome type 24","type":"exact"},{"name":"TCTN2 Joubert syndrome","type":"exact"}],"termid":"MONDO:0014724","xrefs":{"Monarch":{"xref_id":"0014724"}}}


id: GO:0048191
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Strengthening of a bond between peptides. Peptides are compounds of two or more amino acids where the alpha carboxyl group of one is bound to the alpha amino group of another.","definition_xrefs":["GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide stabilization activity (obsolete GO:0048191)","synonyms":[{"name":"peptide stabilization activity","type":"exact"}],"termid":"GO:0048191"}


id: GO:0032087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of a type IV restriction endodeoxyribonuclease activity.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of type IV site-specific deoxyribonuclease activity (obsolete GO:0032087)","synonyms":[{"name":"regulation of type IV restriction endodeoxyribonuclease activity","type":"exact"},{"name":"type IV restriction endodeoxyribonuclease regulator","type":"related"},{"name":"type IV restriction enzyme regulator","type":"related"}],"termid":"GO:0032087"}


id: PBO:0036532
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human COQ3 with an S. pombe MTS","termid":"PBO:0036532"}


id: MONDO:0011239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"disorder of visual system","termid":"MONDO:0024458"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colobomatous macrophthalmia-microcornea syndrome","secondary_identifiers":["OMIM:602499","UMLS:C1865286","GARD:17844","MEDGEN:400728","Orphanet:468672","MESH:C566533"],"synonyms":[{"name":"MACOM","type":"related"},{"name":"MACOM syndrome","type":"exact"},{"name":"macrophthalmia, colobomatous, with microcornea","type":"related"}],"termid":"MONDO:0011239","xrefs":{"Monarch":{"xref_id":"0011239"}}}


id: PBO:0043088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholesterol induced regulator of metabolism RNA","termid":"PBO:0043088"}


id: GO:0021597
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the central nervous system structure. The central nervous system is the core nervous system that serves an integrating and coordinating function. In vertebrates it consists of the brain, spinal cord and spinal nerves. In those invertebrates with a central nervous system it typically consists of a brain, cerebral ganglia and a nerve cord.","definition_xrefs":["GOC:dgh","ISBN:0582227089","GO_REF:0000021","GOC:cls","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"central nervous system morphogenesis","termid":"GO:0021551"}],"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":"central nervous system structural organization","synonyms":[{"name":"central nervous system structural organisation","type":"exact"}],"termid":"GO:0021597"}


id: PBO:0058380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4752","termid":"PBO:0058380"}


id: PBO:0076537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 64 pseudogene","termid":"PBO:0076537"}


id: PBO:0068620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 72, pseudogene","termid":"PBO:0068620"}


id: PBO:0108939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 18","termid":"PBO:0108939"}


id: GO:0035409
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the addition of a phosphate group to a tyrosine residue at position 41 of the histone.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-Y41 phosphorylation (obsolete GO:0035409)","termid":"GO:0035409"}


id: MONDO:1010056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypoparathyroidism that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoparathyroidism, non-human animal","secondary_identifiers":["OMIA:000528"],"termid":"MONDO:1010056","xrefs":{"Monarch":{"xref_id":"1010056"}}}


id: GO:0039519
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus effect a change in the frequency, rate or extent of autophagy in the host.","definition_xrefs":["GOC:bf","GOC:sp"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by virus of host autophagy (obsolete GO:0039519)","synonyms":[{"name":"regulation by virus of host autophagy","type":"exact"}],"termid":"GO:0039519"}


id: GO:0097401
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The acidification of the synaptic vesicle lumen via transport of protons into the vesicle. The resulting electrochemical gradient powers neurotransmitter loading.","definition_xrefs":["GOC:dsf","PMID:22875945","PMID:21172605"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"is_a","term_name":"neuron cellular homeostasis","termid":"GO:0070050"},{"relation_name":"is_a","term_name":"proton transmembrane transport","termid":"GO:1902600"},{"relation_name":"part_of","term_name":"synaptic vesicle maturation","termid":"GO:0016188"},{"relation_name":"part_of","term_name":"synaptic vesicle cycle","termid":"GO:0099504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0055085","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"synaptic vesicle lumen acidification","synonyms":[{"name":"synaptic vesicle lumen pH reduction","type":"exact"},{"name":"synaptic vesicle proton loading","type":"exact"}],"termid":"GO:0097401"}


id: MONDO:0800204
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calvarial doughnut lesions with bone fragility and spondylometaphyseal dysplasia","secondary_identifiers":["MEDGEN:1674505","UMLS:C5193004"],"synonyms":[{"name":"CDLSMD","type":"exact"}],"termid":"MONDO:0800204","xrefs":{"Monarch":{"xref_id":"0800204"}}}


id: PBO:0034597
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_onset_of_metaphase/anaphase_transition_of_meiosis_I","termid":"PBO:0034597"}


id: MONDO:0014147
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the CTSF gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult neuronal ceroid lipofuscinosis","termid":"MONDO:0019260"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0005559","MONDO:0002039","MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"neuronal ceroid lipofuscinosis 13","secondary_identifiers":["Orphanet:352709","UMLS:C3715049","GARD:17527","MEDGEN:811566","OMIM:615362","DOID:0110727"],"synonyms":[{"name":"CLN13","type":"exact"},{"name":"CLN13 disease","type":"related"},{"name":"CTSF neuronal ceroid lipofuscinosis","type":"exact"},{"name":"ceroid lipofuscinosis, neuronal, 13","type":"related"},{"name":"ceroid lipofuscinosis, neuronal, 13 (Kufs type)","type":"exact"},{"name":"ceroid lipofuscinosis, neuronal, 13, Kufs type","type":"related"},{"name":"ceroid lipofuscinosis, neuronal, type 13","type":"exact"},{"name":"neuronal ceroid lipofuscinosis 13 Kufs type","type":"exact"},{"name":"neuronal ceroid lipofuscinosis caused by mutation in CTSF","type":"exact"},{"name":"neuronal ceroid lipofuscinosis type 13","type":"exact"}],"termid":"MONDO:0014147","xrefs":{"Monarch":{"xref_id":"0014147"}}}


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


id: GO:0015047
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADPH + H+ + 2 ferricytochrome c2 = NADP+ + 2 ferrocytochrome c2.","definition_xrefs":["EC:1.6.2.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor","termid":"GO:0016653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"NADPH-cytochrome-c2 reductase activity","secondary_identifiers":["RHEA:15237","MetaCyc:NADPH--CYTOCHROME-C2-REDUCTASE-RXN"],"synonyms":[{"name":"NADPH:ferricytochrome-c2 oxidoreductase activity","type":"related"},{"name":"cytochrome c2 reductase (reduced nicotinamide adinine dinucleotide phosphate, NADPH)","type":"related"},{"name":"reductase, cytochrome c2 (reduced nicotinamide adenine dinucleotide phosphate)","type":"related"}],"termid":"GO:0015047"}


id: GO:0042767
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-dehydro-2,22-dideoxyecdysone + 2 reduced [adrenodoxin] + O2 + 2 H+ = 3-dehydro-2-deoxyecdysone + 2 oxidized [adrenodoxin] + H2O. Other substrates include 3-dehydro-2,22,25-deoxyecdysone and 2,22-dideoxyecdysone.","definition_xrefs":["PMID:12177427","EC:1.14.15.44"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid hydroxylase activity","termid":"GO:0008395"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016713"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"ecdysteroid 22-hydroxylase activity","synonyms":[{"name":"3-dehydro-2,22-dideoxyecdysone 22-hydroxylase activity","type":"narrow"}],"termid":"GO:0042767"}


id: SO:0000225
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding prolyl tRNA (SO:0000268).","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline_tRNA_primary_transcript","synonyms":[{"name":"proline tRNA primary transcript","type":"exact"}],"termid":"SO:0000225"}


id: PR:P0CT84
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl1202 gene.","definition_xrefs":["UniProtKB:P0CT84","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L12-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC31H12.04c","synonyms":[{"name":"Spom972h-rpl1202","type":"exact"}],"termid":"PR:P0CT84"}


id: PBO:0057545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 661","termid":"PBO:0057545"}


id: GO:0039686
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A viral DNA replication process where replication occurs in both directions from the starting point. This creates two replication forks, moving in opposite directions.","definition_xrefs":["GOC:bf","GOC:jl","VZ:1939"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral DNA genome replication","termid":"GO:0039693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"bidirectional double-stranded viral DNA replication","synonyms":[{"name":"viral bidirectional dsDNA replication","type":"exact"}],"termid":"GO:0039686"}


id: GO:0030288
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region between the inner (cytoplasmic or plasma) membrane and outer membrane of organisms with two membranes such as Gram negative bacteria. These periplasmic spaces are relatively thick and contain a thin peptidoglycan layer (PGL), also referred to as a thin cell wall.","definition_xrefs":["GOC:mtg_sensu","GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"periplasmic space","termid":"GO:0042597"},{"relation_name":"part_of","term_name":"cell envelope","termid":"GO:0030313"}],"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":"outer membrane-bounded periplasmic space","secondary_identifiers":["Wikipedia:Periplasmic_space"],"synonyms":[{"name":"outer membrane bounded periplasmic space","type":"exact"},{"name":"outer membrane-enclosed periplasmic space","type":"exact"}],"termid":"GO:0030288"}


id: PBO:0026846
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  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_binucleate_septated_cell","termid":"PBO:0026846"}


id: PBO:0054552
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  {"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 1953","termid":"PBO:0054552"}


id: FYPO:0003855
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). Cells stop growing (and may die) at a concentration of MTT that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002683","FYPO:0001985","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to MTT","synonyms":[{"name":"hypersensitive to MTT","type":"exact"},{"name":"sensitive to 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide","type":"exact"},{"name":"sensitive to MTT during mitotic cell cycle","type":"related"},{"name":"sensitive to MTT during vegetative growth","type":"exact"}],"termid":"FYPO:0003855"}


id: PBO:0086529
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  {"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","termid":"PBO:0086529"}


id: SO:0000591
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  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A tertiary structure in RNA where nucleotides in a loop form base pairs with a region of RNA downstream of the loop.","definition_xrefs":["RSC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_secondary_structure","termid":"SO:0000002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudoknot","secondary_identifiers":["http://en.wikipedia.org/wiki/Pseudoknot"],"termid":"SO:0000591"}


id: MONDO:0100309
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ataxia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0004138","DOID:0050951","ICD10CM:G11","EFO:0009671","icd11.foundation:442347652","MESH:C531684","SCTID:763597000","GARD:20286","MEDGEN:2478","Orphanet:183518","ICD10WHO:G11"],"synonyms":[{"name":"SCA","type":"related"},{"name":"rare hereditary 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id: PR:Q9USY2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A squamous cell carcinoma antigen recognized by T-cells 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04004","PANTHER:PTHR23269:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized RNA-binding protein C1861.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1861.04c","secondary_identifiers":["UniProtKB:Q9USY2"],"synonyms":[{"name":"Spom972h-SART3","type":"exact"}],"termid":"PR:Q9USY2"}


id: PR:O60182
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A replication factor C subunit 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03884","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":"replication factor C subunit 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC23E6.07c","secondary_identifiers":["UniProtKB:O60182"],"synonyms":[{"name":"Spom972h-RFC1","type":"exact"},{"name":"replication factor C1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60182"}


id: MOD:01796
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue containing common isotopes to 1x(13)C,3x(2)H C(6)-labeled L-methionine sulfoxide.","definition_xrefs":["PubMed:18688235","PubMed:15782174"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(2)H deuterium labeled residue","termid":"MOD:00839"},{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"},{"relation_name":"is_a","term_name":"1x(13)C,3x(2)H labeled monomethylated residue","termid":"MOD:01794"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1x(13)C,3x(2)H C(6)-labeled L-methionine sulfoxide","termid":"MOD:01796"}


id: PBO:0050875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IDH3B divergent transcript","termid":"PBO:0050875"}


id: PBO:0042139
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 3","termid":"PBO:0042139"}


id: MONDO:0006190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive epithelial neoplasm arising from the temporal bone. It is characterized by the presence of a papillary pattern, and has been described as an adenoma or carcinoma in the literature. There is disagreement regarding its relationship to endolymphatic sac tumor.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary epithelial neoplasm","termid":"MONDO:0021096"},{"relation_name":"is_a","term_name":"inner ear neoplasm","termid":"MONDO:0024320"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endolymphatic sac tumor","secondary_identifiers":["MEDGEN:389657","EFO:1000230","HP:0030393","ICD9:212.0","UMLS:C2348239","ICDO:8260/1","NCIT:C67560","SCTID:699817008"],"synonyms":[{"name":"ELST","type":"exact"},{"name":"aggressive papillary tumor of the temporal bone","type":"exact"},{"name":"aggressive papillary tumour of the temporal bone","type":"exact"},{"name":"endolymphatic sac neoplasm","type":"exact"},{"name":"endolymphatic sac neoplasm (disease)","type":"exact"},{"name":"endolymphatic sac tumor","type":"exact"},{"name":"endolymphatic sac tumor (disease)","type":"exact"},{"name":"endolymphatic sac tumour (disease)","type":"exact"},{"name":"neoplasm of endolymphatic sac","type":"exact"},{"name":"tumor of endolymphatic sac","type":"exact"},{"name":"tumour of endolymphatic sac","type":"exact"}],"termid":"MONDO:0006190","xrefs":{"Monarch":{"xref_id":"0006190"}}}


id: PBO:0080821
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XXYLT1 antisense RNA 2","termid":"PBO:0080821"}


id: GO:0042277
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  {"annotated_genes":["SJAG_01282","SJAG_02208","SJAG_00702","SJAG_03662","SJAG_01759","SJAG_03729","SJAG_00840","SJAG_04996","SJAG_00326","SJAG_03299","SJAG_01909","SJAG_03684","SJAG_01640","SJAG_02330","SJAG_02998","SJAG_01840","SJAG_02418","SJAG_01488","SJAG_01013","SJAG_03358","SJAG_00962","SJAG_04411","SJAG_03959","SJAG_03781"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77444,60701,57242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030942"},{"annotations":[115628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045015"},{"annotations":[75869,81031,75325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030943"},{"annotations":[80553,76873,98079,75612,77469,79796,95940,74744,75550,78212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008139"},{"annotations":[75600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005052"},{"annotations":[72544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005053"},{"annotations":[92374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033328"},{"annotations":[118644,75105,75514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005048"},{"annotations":[106020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010209"}]},"cv_name":"molecular_function","definition":"Binding to a peptide, an organic compound comprising two or more amino acids linked by peptide bonds.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":24,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null,"SJAG_00840":null,"SJAG_00962":null,"SJAG_01013":null,"SJAG_01282":null,"SJAG_01488":null,"SJAG_01640":null,"SJAG_01759":null,"SJAG_01840":null,"SJAG_01909":null,"SJAG_02208":null,"SJAG_02330":null,"SJAG_02418":null,"SJAG_02998":null,"SJAG_03299":null,"SJAG_03358":null,"SJAG_03662":null,"SJAG_03684":null,"SJAG_03729":null,"SJAG_03781":null,"SJAG_03959":null,"SJAG_04411":null,"SJAG_04996":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"peptide binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0042277","terms_by_termid":{"GO:0005048":null,"GO:0005052":null,"GO:0005053":null,"GO:0008139":null,"GO:0010209":null,"GO:0030942":null,"GO:0030943":null,"GO:0033328":null,"GO:0045015":null}}


id: PBO:0074465
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id: GO:0034607
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The sharp ventral turn performed by the male as he approaches either the hermaphrodite head or tail, whilst trying to locate his partner's vulva. Turning occurs via a sharp ventral coil of the male's tail.","definition_xrefs":["PMID:18050467","WB_REF:WBPaper00002109"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male mating behavior","termid":"GO:0060179"}],"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":"turning behavior involved in mating","synonyms":[{"name":"turning behavior during mating","type":"exact"}],"termid":"GO:0034607"}


id: MONDO:0005800
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute, localized swelling of the eyelid that may be external or internal and usually is a pyogenic (typically staphylococcal) infection or abscess.","direct_ancestors":[{"relation_name":"is_a","term_name":"blepharitis","termid":"MONDO:0004785"},{"relation_name":"is_a","term_name":"staphylococcus aureus infection","termid":"MONDO:0005545"},{"relation_name":"is_a","term_name":"skin disease caused by bacterial infection","termid":"MONDO:0024295"},{"relation_name":"is_a","term_name":"eye infectious disorder","termid":"MONDO:0043885"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005093"],"is_obsolete":false,"name":"hordeolum","secondary_identifiers":["icd11.foundation:1259721857","MEDGEN:6884","DOID:9909","MESH:D006726","NCIT:C118722","SCTID:397513003","UMLS:C0019917"],"synonyms":[{"name":"Stye","type":"exact"},{"name":"blepharitis of eyelid gland","type":"exact"},{"name":"boil of eyelid","type":"exact"},{"name":"eyelid gland blepharitis","type":"exact"},{"name":"furuncle of eyelid","type":"exact"}],"termid":"MONDO:0005800","xrefs":{"Monarch":{"xref_id":"0005800"}}}


id: PBO:0043215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC28 protein kinase regulatory subunit 2","termid":"PBO:0043215"}


id: GO:1990078
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that inhibits multiple events of replication initiation during one replication cycle.","definition_xrefs":["GOC:bhm","PMID:21708944"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"replisome","termid":"GO:0030894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005694","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"replication inhibiting complex","termid":"GO:1990078"}


id: MONDO:0017982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete humeroradial synostosis (obsolete MONDO:0017982)","termid":"MONDO:0017982","xrefs":{"Monarch":{"xref_id":"0017982"}}}


id: MONDO:0002273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited metabolic disorder that involves plasma protein metabolism malfunction.","definition_xrefs":["DOID:2345"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"plasma protein metabolism disease","secondary_identifiers":["UMLS:C3875058","MEDGEN:840208","ICD9:273.8"],"termid":"MONDO:0002273","xrefs":{"Monarch":{"xref_id":"0002273"}}}


id: MONDO:0002610
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A small blood vessel hemorrhage into the skin and/or mucous membranes. Newer lesions appear reddish in color. Older lesions are usually a darker purple color and eventually become a brownish-yellow color.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"purpura","secondary_identifiers":["DOID:3326","UMLS:C0034150","MESH:D011693","SCTID:387778001","MEDGEN:19584","HP:0000979"],"synonyms":[{"name":"purpura","type":"exact"},{"name":"purpura (disease)","type":"exact"},{"name":"purpuric disorder","type":"exact"}],"termid":"MONDO:0002610","xrefs":{"Monarch":{"xref_id":"0002610"}}}


id: PBO:0086479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative mitochondrial ribosomal protein of the large subunit; required for respiratory growth and for efficient translation of mitochondrial COX1 and COX3;  conditional mutant has reduced cytochrome c oxidase activity; protein increases in abundance and relocalizes to the plasma membrane upon DNA replication stress; contains and N-terminal mitochondrial targeting sequence; similar to E. coli L34 ribosomal protein","termid":"PBO:0086479"}


id: MONDO:0008463
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":"split-hand and split-foot with hypodontia","secondary_identifiers":["MESH:C566665","MEDGEN:357125","UMLS:C1866742","OMIM:183500"],"synonyms":[{"name":"split-hand and split-foot with hypodontia","type":"exact"}],"termid":"MONDO:0008463","xrefs":{"Monarch":{"xref_id":"0008463"}}}


id: PBO:0072164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15 pseudogene 1","termid":"PBO:0072164"}


id: MONDO:0002881
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mixed epithelial and mesenchymal neoplasm that arises from the vagina and is characterized by the presence of a malignant mesenchymal component and a benign or atypical mullerian-type epithelial component.","definition_xrefs":["NCIT:C40277"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"vaginal carcinosarcoma","termid":"MONDO:0006488"},{"relation_name":"is_a","term_name":"vaginal cancer","termid":"MONDO:0001402"},{"relation_name":"is_a","term_name":"adenosarcoma","termid":"MONDO:0005636"}],"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":"vaginal adenosarcoma","secondary_identifiers":["DOID:4117","MEDGEN:274378","UMLS:C1519914"],"synonyms":[{"name":"adenosarcoma of vagina","type":"exact"},{"name":"vagina adenosarcoma","type":"exact"},{"name":"vaginal Mullerian adenosarcoma","type":"exact"},{"name":"vaginal Müllerian adenosarcoma","type":"exact"},{"name":"vaginal adenosarcoma","type":"exact"}],"termid":"MONDO:0002881","xrefs":{"Monarch":{"xref_id":"0002881"}}}


id: MONDO:0018267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"combined dystonia","termid":"MONDO:0020065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"combined cervical dystonia","secondary_identifiers":["Orphanet:370114"],"termid":"MONDO:0018267","xrefs":{"Monarch":{"xref_id":"0018267"}}}


id: GO:0030202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving heparin proteoglycans, which consist of a core protein linked to a heparin glycosaminoglycan. The heparin chain is composed of the repeating disaccharide unit beta-(1,4)-N-acetyl-D-glucosamine-alpha-(1,4)-hexuronic acid, the former being either sulfated or deacetylated on its amino group as well as sulfated on one of its hydroxyl groups, and the latter being e a mixture of sulfated and nonsulfated D-glucuronic and L-iduronic acids. Heparin is similar to heparan sulfate but it contains more N-sulfate and O-sulfate groups. Heparin proteoglycans are stored selectively in the secretory granules of mammalian mast cells.","definition_xrefs":["PMID:22566225"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteoglycan metabolic process","termid":"GO:0006029"}],"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":"heparin proteoglycan metabolic process","synonyms":[{"name":"heparan sulfate metabolic process","type":"related"},{"name":"heparin metabolism","type":"exact"}],"termid":"GO:0030202"}


id: MONDO:0000166
data:
  {"annotated_genes":["SJAG_02520"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011953"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"post-infectious disorder","termid":"MONDO:0021669"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02520":null},"genotype_count":0,"is_obsolete":false,"name":"encephalopathy, acute, infection-induced","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:610551"],"termid":"MONDO:0000166","terms_by_termid":{"MONDO:0011953":null},"xrefs":{"Monarch":{"xref_id":"0000166"}}}


id: FYPO:0005110
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 export of sodium ions out of a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal transport","termid":"FYPO:0001071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0000257","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal sodium export","synonyms":[{"name":"normal cellular sodium export","type":"exact"},{"name":"normal sodium export during mitotic cell cycle","type":"related"},{"name":"normal sodium export during vegetative growth","type":"exact"},{"name":"normal sodium export from cell","type":"exact"},{"name":"normal sodium ion export","type":"exact"}],"termid":"FYPO:0005110"}


id: PBO:0049487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H1.9 linker histone, pseudogene","termid":"PBO:0049487"}


id: FYPO:0002912
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an inviable cell that does not divide, is elongated, and contains more than one nucleus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated multinucleate vegetative cell","termid":"FYPO:0001493"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, elongated cell","termid":"FYPO:0004603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000032","FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000005","FYPO:0000631"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, elongated multinucleate cell","synonyms":[{"name":"inviable after spore germination, multinucleate elongated cell","type":"exact"},{"name":"inviable after spore germination, undivided elongated multinucleate cell","type":"exact"},{"name":"inviable following spore germination, without cell division, elongated multinucleate cell","type":"exact"},{"name":"inviable germinated spore, without cell division, elongated multinucleate cell","type":"exact"},{"name":"lethal after spore germination, without cell division, elongated multinucleate cell","type":"exact"}],"termid":"FYPO:0002912"}


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


id: MONDO:0016575
data:
  {"annotated_genes":["SJAG_03794"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014909"}]},"cv_name":"mondo","definition":"A rare, genetically heterogeneous, primarily respiratory disorder characterized by chronic upper and lower respiratory tract disease. Approximately half of PCD patients have an organ laterality defect (situs inversus totalis or situs ambiguus/heterotaxy).","definition_xrefs":["Orphanet:244"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete male infertility due to sperm motility disorder (obsolete MONDO:0018395)","termid":"MONDO:0018395"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"ciliopathy","termid":"MONDO:0005308"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03794":null},"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1713839459","MESH:D007619","DOID:9562","NANDO:2200204","UMLS:C0008780","MEDGEN:3467","NCIT:C84797","MedDRA:10069713","NANDO:2200203","GARD:4484","OMIMPS:244400","SCTID:42402006","DOID:0050144","MESH:D002925","NORD:1605","NANDO:2100034","SCTID:86204009"],"synonyms":[{"name":"Dextrocardia bronchiectasis and sinusitis","type":"related"},{"name":"Dextrocardia-bronchiectasis-sinusitis syndrome","type":"related"},{"name":"ICS","type":"related"},{"name":"Immotile cilia syndrome, Kartagener type","type":"related"},{"name":"Kartagener syndrome","type":"exact"},{"name":"Kartagener's syndrome","type":"exact"},{"name":"PCD","type":"exact"},{"name":"Primary ciliary dyskinesia and situs inversus","type":"related"},{"name":"Primary ciliary dyskinesia, Kartagener type","type":"related"},{"name":"Siewert syndrome","type":"related"},{"name":"bronchiectasis, chronic sinusitis and dextrocardia syndrome","type":"related"},{"name":"ciliary dyskinesia primary","type":"related"},{"name":"ciliary motility disorder","type":"exact"},{"name":"immotile ciliary syndrome","type":"exact"}],"termid":"MONDO:0016575","terms_by_termid":{"MONDO:0014909":null},"xrefs":{"Monarch":{"xref_id":"0016575"}}}


id: GO:0047177
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-alkyl-2-lyso-sn-glycero-3-phosphoethanolamine + 1-alkyl-2-arachidonyl-sn-glycero-3-phosphocholine = 1-alkyl-2-lyso-sn-glycero-3-phosphocholine + 1-alkyl-2-arachidonyl-sn-glycero-3-phosphoethanolamine.","definition_xrefs":["EC:2.3.1.147","MetaCyc:2.3.1.147-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"glycerophospholipid arachidonoyl-transferase (CoA-independent) activity","secondary_identifiers":["RHEA:15409"],"synonyms":[{"name":"1-organyl-2-arachidonoyl-sn-glycero-3-phosphocholine:1-organyl-2-lyso-sn-glycero-3-phosphoethanolamine arachidonoyltransferase (CoA-independent)","type":"related"},{"name":"1-organyl-2-arachidonyl-sn-glycero-3-phosphocholine:1-organyl-2-lyso-sn-glycero-3-phosphoethanolamine arachidonoyltransferase (CoA-independent)","type":"related"}],"termid":"GO:0047177"}


id: PBO:0082838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Constituent of 66S pre-ribosomal particles; required for ribosomal large subunit maturation; functionally redundant with Ssf2p; member of the Brix family; SSF1 has a paralog, SSF2, that arose from the whole genome duplication","termid":"PBO:0082838"}


id: PBO:0117172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLDND1 antisense RNA 1","termid":"PBO:0117172"}


id: GO:1901345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a L-thialysine stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to amino acid","termid":"GO:0043200"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to L-thialysine","synonyms":[{"name":"response to thialysine","type":"broad"}],"termid":"GO:1901345"}


id: GO:0007494
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the midgut over time, from its formation to the mature structure. The midgut is the middle part of the alimentary canal from the stomach, or entrance of the bile duct, to, or including, the large intestine.","definition_xrefs":["GOC:jid","UBERON:0001045"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive tract development","termid":"GO:0048565"}],"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":"midgut development","termid":"GO:0007494"}


id: PBO:0003709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA transporter (predicted)","termid":"PBO:0003709"}


id: PBO:0072900
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 11","termid":"PBO:0072900"}


id: GO:0021894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a cerebral cortex GABAergic interneuron over time, from initial commitment to its fate, to the fully functional differentiated cell.","definition_xrefs":["GO_REF:0000021","PMID:12626695","GOC:cls","GOC:dph","GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"forebrain neuron development","termid":"GO:0021884"},{"relation_name":"part_of","term_name":"cerebral cortex GABAergic interneuron differentiation","termid":"GO:0021892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebral cortex GABAergic interneuron development","termid":"GO:0021894"}


id: MONDO:0000319
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete infant botulism (obsolete MONDO:0000319)","termid":"MONDO:0000319","xrefs":{"Monarch":{"xref_id":"0000319"}}}


id: PBO:0073377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sestrin 1","termid":"PBO:0073377"}


id: MONDO:0008316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary thrombophilia due to congenital protein C deficiency","termid":"MONDO:0019145"}],"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":"thrombophilia due to protein C deficiency, autosomal dominant","secondary_identifiers":["MEDGEN:436138","UMLS:C2674321","DOID:0111909","GARD:18574","OMIM:176860"],"synonyms":[{"name":"Proc deficiency, autosomal dominant","type":"related"},{"name":"Protein C deficiency, acquired","type":"related"},{"name":"Protein C deficiency, autosomal dominant","type":"related"},{"name":"THPH3","type":"related"},{"name":"thrombophilia 3 due to protein C deficiency, autosomal dominant","type":"exact"},{"name":"thrombophilia due to PROTEIN C deficiency, autosomal dominant","type":"related"},{"name":"thrombophilia due to protein C deficiency, autosomal dominant","type":"exact"}],"termid":"MONDO:0008316","xrefs":{"Monarch":{"xref_id":"0008316"}}}


id: PBO:0058466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5195","termid":"PBO:0058466"}


id: PBO:0005180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation elongation factor 2 (EF-2) Eft2,B","termid":"PBO:0005180"}


id: MONDO:0054868
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Small intestinal obstruction that results from the impaction of thick meconium in the distal small intestine.","definition_xrefs":["NCIT:C98979"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ileus","termid":"MONDO:0004567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"meconium ileus","secondary_identifiers":["MESH:D000074270","MEDGEN:473705","SCTID:206523001","UMLS:C2939175"],"synonyms":[{"name":"meconium ileus","type":"exact"}],"termid":"MONDO:0054868","xrefs":{"Monarch":{"xref_id":"0054868"}}}


id: GO:0019940
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete SUMO-dependent protein catabolic process (obsolete GO:0019940)","synonyms":[{"name":"SUMO-dependent protein breakdown","type":"exact"},{"name":"SUMO-dependent protein catabolic process","type":"exact"},{"name":"SUMO-dependent protein catabolism","type":"exact"},{"name":"SUMO-dependent protein degradation","type":"exact"}],"termid":"GO:0019940"}


id: PBO:0079571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin B pseudogene 3","termid":"PBO:0079571"}


id: GO:0046606
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the centrosome cycle.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"regulation of centrosome cycle","termid":"GO:0046605"},{"relation_name":"is_a","term_name":"negative regulation of cytoskeleton organization","termid":"GO:0051494"},{"relation_name":"negatively_regulates","term_name":"centrosome cycle","termid":"GO:0007098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0007010","GO:0008150"],"is_obsolete":false,"name":"negative regulation of centrosome cycle","synonyms":[{"name":"down regulation of centrosome cycle","type":"exact"},{"name":"down-regulation of centrosome cycle","type":"exact"},{"name":"downregulation of centrosome cycle","type":"exact"},{"name":"inhibition of centrosome cycle","type":"narrow"}],"termid":"GO:0046606"}


id: PBO:0077058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THSD4 antisense RNA 1","termid":"PBO:0077058"}


id: MONDO:0005831
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tuberculosis of the lymph node.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrapulmonary tuberculosis","termid":"MONDO:0000368"},{"relation_name":"is_a","term_name":"lymph node disorder","termid":"MONDO:0004928"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"lymph node tuberculosis","secondary_identifiers":["MESH:D014388","ICD10CM:A18.2","UMLS:C0041316","SCTID:10893003","EFO:0007350","MEDGEN:11946","NCIT:C26896","DOID:4889"],"synonyms":[{"name":"king's evil","type":"exact"},{"name":"lymph node tuberculosis","type":"exact"},{"name":"scrofula","type":"exact"},{"name":"tuberculous adenitis","type":"exact"},{"name":"tuberculous lymphadenopathy","type":"exact"}],"termid":"MONDO:0005831","xrefs":{"Monarch":{"xref_id":"0005831"}}}


id: GO:1905959
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cellular response to alcohol.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:26434723"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of response to alcohol","termid":"GO:1901421"},{"relation_name":"is_a","term_name":"regulation of cellular response to alcohol","termid":"GO:1905957"},{"relation_name":"positively_regulates","term_name":"cellular response to alcohol","termid":"GO:0097306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cellular response to alcohol","synonyms":[{"name":"activation of cellular response to alcohol","type":"narrow"},{"name":"up regulation of cellular response to alcohol","type":"exact"},{"name":"up-regulation of cellular response to alcohol","type":"exact"},{"name":"upregulation of cellular response to alcohol","type":"exact"}],"termid":"GO:1905959"}


id: SOFP:evidenceGB
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"evidenceGB","termid":"SOFP:evidenceGB"}


id: PBO:0001929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinate phosphoribosyltransferase (predicted)","termid":"PBO:0001929"}


id: PBO:0058558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6500","termid":"PBO:0058558"}


id: PBO:0075081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 131","termid":"PBO:0075081"}


id: GO:0061935
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The binding and fusion of a sperm, with the plasma membrane of the oocyte as part of the process of double fertilization forming two zygotes.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"is_a","term_name":"plasma membrane fusion","termid":"GO:0045026"},{"relation_name":"part_of","term_name":"double fertilization forming two zygotes","termid":"GO:0009677"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"fusion of sperm to egg plasma membrane involved in double fertilization forming two zygotes","termid":"GO:0061935"}


id: MONDO:0957783
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited ichthyosis","termid":"MONDO:0015947"}],"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":"ichthyosis with erythrokeratoderma","secondary_identifiers":["OMIM:620507","UMLS:C5882691","MEDGEN:1852819"],"termid":"MONDO:0957783","xrefs":{"Monarch":{"xref_id":"0957783"}}}


id: PBO:0003177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L25 (predicted)","termid":"PBO:0003177"}


id: GO:0002361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a CD4-positive, CD25-positive, alpha-beta regulatory T cell.","definition_xrefs":["GOC:add","PMID:15207821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CD4-positive, alpha-beta T cell differentiation","termid":"GO:0043367"},{"relation_name":"is_a","term_name":"regulatory T cell differentiation","termid":"GO:0045066"}],"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":"CD4-positive, CD25-positive, alpha-beta regulatory T cell differentiation","synonyms":[{"name":"CD4-positive, CD25-positive, alpha-beta regulatory T cell development","type":"related"},{"name":"CD4-positive, CD25-positive, alpha-beta regulatory T lymphocyte differentiation","type":"exact"},{"name":"CD4-positive, CD25-positive, alpha-beta regulatory T-cell differentiation","type":"exact"},{"name":"CD4-positive, CD25-positive, alpha-beta regulatory T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002361"}


id: PBO:0026889
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-translation_regulation_phenotype_during_vegetative_growth","termid":"PBO:0026889"}


id: GO:0003180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the structure of the aortic valve is generated and organized.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart valve morphogenesis","termid":"GO:0003179"},{"relation_name":"part_of","term_name":"aortic valve development","termid":"GO:0003176"}],"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":"aortic valve morphogenesis","termid":"GO:0003180"}


id: MONDO:0008121
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":"onychogryposis, pedal, with keratosis plantaris and coarse hair","secondary_identifiers":["MESH:C563506","MEDGEN:331637","OMIM:164680","UMLS:C1833997"],"synonyms":[{"name":"onychogryposis, pedal, with keratosis plantaris and coarse hair","type":"exact"}],"termid":"MONDO:0008121","xrefs":{"Monarch":{"xref_id":"0008121"}}}


id: PBO:0054768
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 2180","termid":"PBO:0054768"}


id: PBO:0073198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEM1 26S proteasome subunit","termid":"PBO:0073198"}


id: GO:0060118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a vestibular receptor cell over time, from its formation to the mature structure. Cell development does not include the steps involved in committing a cell to a specific fate.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner ear receptor cell development","termid":"GO:0060119"},{"relation_name":"part_of","term_name":"vestibular receptor cell differentiation","termid":"GO:0060114"}],"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":"vestibular receptor cell development","synonyms":[{"name":"vestibular hair cell development","type":"exact"}],"termid":"GO:0060118"}


id: GO:0051408
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: glyceraldehyde 3-phosphate(out) + phosphate(in) = glyceraldehyde 3-phosphate(in) + phosphate(out).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"triose-phosphate:phosphate antiporter activity","termid":"GO:0009670"}],"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:0003674","GO:0022857"],"is_obsolete":false,"name":"glyceraldehyde 3-phosphate:phosphate antiporter activity","synonyms":[{"name":"glyceraldehyde 3-phosphate:inorganic phosphate antiporter activity","type":"exact"}],"termid":"GO:0051408"}


id: PBO:0056356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP9 antisense RNA 1","termid":"PBO:0056356"}


id: PBO:0069973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1268, pseudogene","termid":"PBO:0069973"}


id: GO:0002843
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of tolerance induction to tumor cell.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of peripheral tolerance induction","termid":"GO:0002658"},{"relation_name":"is_a","term_name":"regulation of immune response to tumor cell","termid":"GO:0002837"},{"relation_name":"regulates","term_name":"tolerance induction to tumor cell","termid":"GO:0002413"}],"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 tolerance induction to tumor cell","synonyms":[{"name":"regulation of tolerance induction to tumour cell","type":"exact"}],"termid":"GO:0002843"}


id: GO:0019242
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of methylglyoxal, CH3-CO-CHO, the aldehyde of pyruvic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylglyoxal metabolic process","termid":"GO:0009438"},{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"aldehyde biosynthetic process","termid":"GO:0046184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"methylglyoxal biosynthetic process","synonyms":[{"name":"methylglyoxal anabolism","type":"exact"},{"name":"methylglyoxal biosynthesis","type":"exact"},{"name":"methylglyoxal formation","type":"exact"},{"name":"methylglyoxal synthesis","type":"exact"}],"termid":"GO:0019242"}


id: MONDO:1012501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hydrallantois, non-human animal","termid":"MONDO:1011672"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrallantois, water buffalo","secondary_identifiers":["OMIA:002053-89462"],"termid":"MONDO:1012501","xrefs":{"Monarch":{"xref_id":"1012501"}}}


id: GO:0007141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cell cycle process comprising the steps by which a cell progresses through male meiosis I, the first meiotic division in the male germline.","definition_xrefs":["GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiosis I","termid":"GO:0007127"},{"relation_name":"is_a","term_name":"male meiotic nuclear division","termid":"GO:0007140"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0008150","GO:0140013","GO:0007049"],"is_obsolete":false,"name":"male meiosis I","synonyms":[{"name":"male meiosis I nuclear division","type":"exact"}],"termid":"GO:0007141"}


id: MONDO:0016096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant germ cell tumor other than dysgerminoma that arises from the ovary.","definition_xrefs":["NCIT:C102870"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian primitive germ cell tumor","termid":"MONDO:0003408"},{"relation_name":"is_a","term_name":"nongerminomatous germ cell tumor","termid":"MONDO:0021656"}],"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":"malignant non-dysgerminomatous germ cell tumor of ovary","secondary_identifiers":["GARD:20349","MEDGEN:1826164","Orphanet:206538","UMLS:C5679783"],"synonyms":[{"name":"non-dysgerminomatous germ cell cancer of ovary","type":"exact"},{"name":"ovarian Nondysgerminomatous germ cell tumor","type":"exact"},{"name":"ovarian Nondysgerminomatous germ cell tumour","type":"exact"},{"name":"ovarian non-dysgerminomatous germ cell tumor","type":"exact"},{"name":"ovarian non-dysgerminomatous germ cell tumour","type":"exact"}],"termid":"MONDO:0016096","xrefs":{"Monarch":{"xref_id":"0016096"}}}


id: GO:0051234
data:
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id: PBO:0084079
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id: GO:0090710
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-5-phosphomevalonate + ATP = ADP + CO2 + isopentenyl phosphate + phosphate.","definition_xrefs":["PMID:24375100","RHEA:40955"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"phosphomevalonate decarboxylase activity","secondary_identifiers":["EC:4.1.1.99","MetaCyc:RXN-10067"],"termid":"GO:0090710"}


id: PBO:0063979
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id: GO:0043063
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id: MONDO:0016009
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fetal trimethadione syndrome is a drug-related embryofetopathy that can occur when an embryo/fetus is exposed to trimethadione and that is characterized by pre- and post-natal growth retardation, intellectual deficit, developmental and speech delay, craniofacial anomalies (with some similarities to those seen in fetal valproate syndrome), and less commonly, cleft palate, malformations of the heart, urogenital system and limbs. Trimethadione is an antiepileptic drug that has been removed from the market in Europe and is no longer used much in other countries due to teratogenicity and potential side effects.","definition_xrefs":["Orphanet:1913"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxic or drug-related embryofetopathy","termid":"MONDO:0016677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fetal trimethadione syndrome","secondary_identifiers":["UMLS:C0265373","GARD:18750","icd11.foundation:1743242235","MESH:C537798","MEDGEN:120538","SCTID:66351003","ICD9:759.89"],"termid":"MONDO:0016009","xrefs":{"Monarch":{"xref_id":"0016009"}}}


id: GO:0060479
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells, e.g. embryonic or regenerative cells, acquire specialized structural and/or functional features of a mature cell found in the lung. Differentiation includes the processes involved in commitment of a cell to a specific fate.","definition_xrefs":["GOC:dph","GOC:mtg_lung"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"lung development","termid":"GO:0030324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lung cell differentiation","synonyms":[{"name":"pulmonary cell differentiation","type":"exact"}],"termid":"GO:0060479"}


id: GO:1904414
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardiac ventricle development.","definition_xrefs":["PMID:19590510","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of cardiac ventricle development","termid":"GO:1904412"},{"relation_name":"positively_regulates","term_name":"cardiac ventricle development","termid":"GO:0003231"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cardiac ventricle development","synonyms":[{"name":"activation of cardiac ventricle development","type":"narrow"},{"name":"up regulation of cardiac ventricle development","type":"exact"},{"name":"up-regulation of cardiac ventricle development","type":"exact"},{"name":"upregulation of cardiac ventricle development","type":"exact"}],"termid":"GO:1904414"}


id: PBO:0039386
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amylase alpha 1C","termid":"PBO:0039386"}


id: PBO:0058433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4803","termid":"PBO:0058433"}


id: PBO:0056207
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member B2","termid":"PBO:0056207"}


id: MONDO:0958205
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Yuksel-Vogel-Bauer syndrome","secondary_identifiers":["MEDGEN:1847314","OMIM:620703","UMLS:C5882751"],"termid":"MONDO:0958205","xrefs":{"Monarch":{"xref_id":"0958205"}}}


id: GO:0106130
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  {"annotated_genes":["SJAG_01859","SJAG_06634"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003999"},{"annotations":[95708],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052657"},{"annotations":[77527],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004422"},{"annotations":[95711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000310"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: RMP + diphosphate = R + 5-phospho-alpha-D-ribose 1-diphosphate.","definition_xrefs":["PMID:5123876"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01859":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016757","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"purine phosphoribosyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-74215","Reactome:R-HSA-9734274","Reactome:R-HSA-9748951"],"termid":"GO:0106130","terms_by_termid":{"GO:0000310":null,"GO:0003999":null,"GO:0004422":null,"GO:0052657":null}}


id: PBO:0055524
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  {"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 2958","termid":"PBO:0055524"}


id: PBO:0004704
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme Ubc8 (predicted)","termid":"PBO:0004704"}


id: FYPO:0001156
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which cells cause the pH of their growth medium to decrease by a greater amount than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered effect on growth medium","termid":"FYPO:0001155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001155"}],"interesting_parent_ids":["FYPO:0001155","FYPO:0001985"],"is_obsolete":false,"name":"decreased pH of growth medium","synonyms":[{"name":"decreased pH level of growth medium","type":"exact"},{"name":"increased growth medium acidification","type":"exact"},{"name":"reduced pH of growth medium","type":"exact"}],"termid":"FYPO:0001156"}


id: GO:0060933
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a His-Purkinje cell over time, from its formation to the mature state. These cells form the fibers that regulate cardiac muscle contraction in the ventricles.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac cell development","termid":"GO:0055006"},{"relation_name":"part_of","term_name":"His-Purkinje system cell differentiation","termid":"GO:0060932"}],"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":"His-Purkinje system cell development","termid":"GO:0060933"}


id: PBO:0044563
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deleted in azoospermia 4","termid":"PBO:0044563"}


id: GO:0046799
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The recruitment of the helicase-primase complex to viral DNA lesions during viral DNA repair.","definition_xrefs":["ISBN:0781718325"],"gene_count":0,"genotype_count":0,"name":"obsolete recruitment of helicase-primase complex to DNA lesions (obsolete GO:0046799)","termid":"GO:0046799"}


id: PBO:0087084
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L43B; homologous to mammalian ribosomal protein L37A, no bacterial homolog; RPL43B has a paralog, RPL43A, that arose from the whole genome duplication; protein abundance increases in response to DNA replication stress","termid":"PBO:0087084"}


id: GO:0016929
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id: GO:0098556
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the rough endoplasmic reticulum membrane that faces the cytoplasm.","definition_xrefs":["GOC:ab","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic side of endoplasmic reticulum membrane","termid":"GO:0098554"},{"relation_name":"part_of","term_name":"rough endoplasmic reticulum membrane","termid":"GO:0030867"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005789"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005783"}],"interesting_parent_ids":["GO:0005737","GO:0005783","GO:0005789","GO:0005575"],"is_obsolete":false,"name":"cytoplasmic side of rough endoplasmic reticulum membrane","termid":"GO:0098556"}


id: PBO:0085090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear exosome-associated nucleic acid binding protein; involved in RNA processing, surveillance, degradation, tethering, and export; forms a stable heterodimer with Rrp6p and regulates its exonucleolytic activity; rapidly degraded by the proteasome in the absence of Rrp6p; homolog of mammalian nuclear matrix protein C1D involved in regulation of DNA repair and recombination","termid":"PBO:0085090"}


id: PBO:0044203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cathepsin L pseudogene 1","termid":"PBO:0044203"}


id: PBO:0061317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore complex interacting protein family member A2","termid":"PBO:0061317"}


id: PBO:0039550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD44 intronic transcript 1","termid":"PBO:0039550"}


id: GO:0050575
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-(S)-hydroxypropyl-coenzyme M + NAD+ = 2-oxopropyl-coenzyme M + H+ + NADH.","definition_xrefs":["EC:1.1.1.269","RHEA:21052"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"2-(S)-hydroxypropyl-CoM dehydrogenase activity","secondary_identifiers":["UM-BBD_reactionID:r0853","KEGG_REACTION:R05690","MetaCyc:1.1.1.269-RXN"],"synonyms":[{"name":"2-(2-(S)-hydroxypropylthio)ethanesulfonate dehydrogenase activity","type":"related"},{"name":"2-[2-(S)-hydroxypropylthio]ethanesulfonate:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0050575"}


id: GO:0090332
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of closing of stomata, pores in the epidermis of leaves and stems bordered by two guard cells and serving in gas exchange.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stomatal movement","termid":"GO:0010118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"stomatal closure","termid":"GO:0090332"}


id: SO:0001518
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An inversion event that includes the centromere.","direct_ancestors":[{"relation_name":"is_a","term_name":"inversion_attribute","termid":"SO:0001517"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pericentric","termid":"SO:0001518"}


id: PBO:0121006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDAP1 pseudogene 3","termid":"PBO:0121006"}


id: PBO:0046564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K member 6, envelope","termid":"PBO:0046564"}


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


id: GO:0021685
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the cerebellar granule layer. This process pertains to the physical shaping of a rudimentary structure. The granular layer is the innermost layer of the cerebellar cortex. This layer contains densely packed small neurons, mostly granule cells. Some Golgi cells are found at the outer border. Granule neurons send parallel fibers to the upper molecular layer, where they synapse with Purkinje cell dendrites. Mossy fibers from the pontine nuclei in the white matter synapse with granule cell axons, Golgi cell axons and unipolar brush interneuron axons at cerebellar glomeruli in the granule cell layer.","definition_xrefs":["GOC:jid","ISBN:0838580343","GOC:dgh","GO_REF:0000021","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"cerebellar granular layer morphogenesis","termid":"GO:0021683"},{"relation_name":"part_of","term_name":"cerebellar cortex structural organization","termid":"GO:0021698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebellar granular layer structural organization","synonyms":[{"name":"cerebellar granular layer structural organisation","type":"exact"}],"termid":"GO:0021685"}


id: MONDO:0015149
data:
  {"annotated_genes":["SJAG_01848","SJAG_04506","SJAG_00199","SJAG_04325","SJAG_05289","SJAG_04292"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87620],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011489"},{"annotations":[87095,87097,87096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012256"},{"annotations":[88686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012928"},{"annotations":[87543],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014282"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00199":null,"SJAG_01848":null,"SJAG_04292":null,"SJAG_04325":null,"SJAG_04506":null,"SJAG_05289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"pure hereditary spastic paraplegia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:19822","MEDGEN:581445","UMLS:C0393555","SCTID:230260007","NANDO:1200053","Orphanet:102012"],"synonyms":[{"name":"Pure HSP","type":"exact"},{"name":"Pure SPG","type":"exact"},{"name":"Pure familial spastic paraplegia","type":"exact"},{"name":"uncomplicated HSP","type":"exact"},{"name":"uncomplicated SPG","type":"exact"},{"name":"uncomplicated familial spastic paraplegia","type":"exact"},{"name":"uncomplicated hereditary spastic paraplegia","type":"exact"}],"termid":"MONDO:0015149","terms_by_termid":{"MONDO:0011489":null,"MONDO:0012256":null,"MONDO:0012928":null,"MONDO:0014282":null},"xrefs":{"Monarch":{"xref_id":"0015149"}}}


id: GO:0016975
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Inhibition of proteinase by a mechanism involving a bait region which contains specific sites, cleavage of which induces a conformational change that results in trapping of the proteinase; following cleavage in the bait region a thiolester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase; subsequently epsilon-amino groups of the proteinase react with thiolester linkages in the inhibitor to form stable amide links; the entrapped proteinase can now only act on low molecular mass substrates.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete alpha-2 macroglobulin (obsolete GO:0016975)","synonyms":[{"name":"alpha-2 macroglobulin","type":"exact"}],"termid":"GO:0016975"}


id: GO:0039598
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a virus increases the frequency, rate or extent of the breakdown of host messenger RNA (mRNA) initiated by the enzymatic addition of a sequence of adenylyl residues (polyadenylation) at the 3' end the target mRNA.","definition_xrefs":["GOC:sp"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by virus of host nuclear polyadenylation-dependent mRNA catabolic process (obsolete GO:0039598)","synonyms":[{"name":"induction by virus of host nuclear poly(A)-dependent mRNA catabolic process","type":"related"},{"name":"induction by virus of host nuclear polyadenylation-dependent mRNA catabolic process","type":"exact"},{"name":"virus-mediated host mRNA decay by hyperadenylation","type":"narrow"}],"termid":"GO:0039598"}


id: PR:O14260
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC7D4.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14260"],"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":"UPF0592 membrane protein C7D4.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC7D4.03c","synonyms":[{"name":"Spom972h-SPAC7D4.03c","type":"exact"}],"termid":"PR:O14260"}


id: PBO:0065989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recombination activating 1","termid":"PBO:0065989"}


id: GO:0006655
data:
  {"annotated_genes":["SJAG_00168","SJAG_03563","SJAG_03700","SJAG_04317"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81938,73156,94988,119851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032049"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phosphatidylglycerols, any of a class of phospholipids in which the phosphatidyl group is esterified to the hydroxyl group of glycerol.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylglycerol metabolic process","termid":"GO:0046471"},{"relation_name":"is_a","term_name":"glycerophospholipid biosynthetic process","termid":"GO:0046474"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00168":null,"SJAG_03563":null,"SJAG_03700":null,"SJAG_04317":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"phosphatidylglycerol biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-1483148"],"synonyms":[{"name":"phosphatidylglycerol anabolism","type":"exact"},{"name":"phosphatidylglycerol biosynthesis","type":"exact"},{"name":"phosphatidylglycerol formation","type":"exact"},{"name":"phosphatidylglycerol synthesis","type":"exact"}],"termid":"GO:0006655","terms_by_termid":{"GO:0032049":null}}


id: MONDO:0015775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nonrhizomelic chondrodysplasia punctata is a form of chondrodysplasia punctata, a group of diseases in which the common characteristic is bone calcifications near joints from birth. Nonrhizomelic chondrodysplasia punctata is not an entity in itself but covers several diseases with variable clinical findings and modes of transmission.","definition_xrefs":["Orphanet:176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chondrodysplasia punctata","termid":"MONDO:0019701"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-rhizomelic chondrodysplasia punctata","secondary_identifiers":["GARD:18679","MEDGEN:1842643","UMLS:C5681009"],"termid":"MONDO:0015775","xrefs":{"Monarch":{"xref_id":"0015775"}}}


id: PBO:0039826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor related protein 1","termid":"PBO:0039826"}


id: PBO:0060987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NGRN pseudogene 3","termid":"PBO:0060987"}


id: GO:0036118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that results in the aggregation, arrangement and bonding together of a hyaluranon cable, a cable structure, surrounding some cell types (e.g. proximal or bronchial tubular epithelial cells), and composed of hyaluranon (HA), a ubiquitous connective tissue glycosaminoglycan.","definition_xrefs":["PMID:16900089","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"hyaluranon cable assembly","synonyms":[{"name":"HA cable assembly","type":"exact"}],"termid":"GO:0036118"}


id: PBO:0090412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L15","termid":"PBO:0090412"}


id: GO:0046347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of mannosomine, 2-amino-2-deoxymannose; the D-isomer is a constituent of neuraminic acids as well as mucolipids and mucoproteins.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino sugar biosynthetic process","termid":"GO:0046349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mannosamine biosynthetic process","synonyms":[{"name":"mannosamine anabolism","type":"exact"},{"name":"mannosamine biosynthesis","type":"exact"},{"name":"mannosamine formation","type":"exact"},{"name":"mannosamine synthesis","type":"exact"}],"termid":"GO:0046347"}


id: PBO:0076832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomerase RNA component","termid":"PBO:0076832"}


id: GO:1905544
data:
  {"annotated_genes":["SJAG_00991"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95278],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905626"}]},"cv_name":"biological_process","definition":"The directed movement of L-methionine from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:TermGenie","PMID:17556368","GO_REF:0000075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"},{"relation_name":"is_a","term_name":"methionine import across plasma membrane","termid":"GO:1903692"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00991":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"L-methionine import across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1903813"],"synonyms":[{"name":"L-methionine import into cell","type":"exact"}],"termid":"GO:1905544","terms_by_termid":{"GO:1905626":null}}


id: MONDO:0043089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an acquired, inflammatory eye condition affecting the retina, retinal pigment epithelium (pigmented layer of the retina), and choroid. It usually affects both eyes and is characterized by multiple, yellow-white lesions in the back of the eye. The condition can significantly impair visual acuity if the macula is involved. APMPPE typically resolves on its own in weeks to months. While the cause is unknown, about a third of cases appear to develop after a flu-like illness. Non-ocular symptoms are uncommon, but cerebral vasculitis can be present and may cause permanent and/or severe neurological complications.","definition_xrefs":["GARD:0002183"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"multifocal choroiditis","termid":"MONDO:0023833"}],"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":"acute posterior multifocal placoid pigment epitheliopathy","secondary_identifiers":["GARD:2183","MEDGEN:56348","ICD10CM:H30.14","NORD:1101","icd11.foundation:2036282532","UMLS:C0154884","SCTID:89188001"],"synonyms":[{"name":"AMPPE","type":"related"},{"name":"APMPPE","type":"related"},{"name":"Epitheliopathy, Acute Posterior Multifocal Placoid Pigment","type":"exact"},{"name":"acute multifocal placoid pigment epitheliopathy","type":"related"},{"name":"acute placoid pigment epitheliopathy","type":"related"},{"name":"acute posterior multifocal placoid pigment epitheliopathy","type":"exact"},{"name":"amppe - acute multifocal placoid pigment epitheliopathy","type":"related"},{"name":"apmppe","type":"related"},{"name":"epitheliopathy, acute posterior multifocal placoid pigment","type":"related"},{"name":"multifocal placoid pigment epitheliopathy","type":"related"},{"name":"pigment epitheliopathy, disseminated retinitis and retinochoroiditis","type":"related"}],"termid":"MONDO:0043089","xrefs":{"Monarch":{"xref_id":"0043089"}}}


id: GO:0002517
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process involving any mechanism for tolerance induction in T cells.","definition_xrefs":["ISBN:0781735149","GOC:jal","PMID:16551263"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tolerance induction","termid":"GO:0002507"}],"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 tolerance induction","synonyms":[{"name":"T lymphocyte tolerance induction","type":"exact"},{"name":"T-cell tolerance induction","type":"exact"},{"name":"T-lymphocyte tolerance induction","type":"exact"}],"termid":"GO:0002517"}


id: GO:0019607
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of phenylethylamine, an amine with pharmacological properties similar to those of amphetamine, occurs naturally as a neurotransmitter in the brain, and is present in chocolate and oil of bitter almonds.","definition_xrefs":["GOC:jl","ISBN:0395825172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biogenic amine catabolic process","termid":"GO:0042402"},{"relation_name":"is_a","term_name":"phenylethylamine metabolic process","termid":"GO:0042443"},{"relation_name":"is_a","term_name":"primary amino compound catabolic process","termid":"GO:1901161"}],"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":"phenylethylamine catabolic process","secondary_identifiers":["MetaCyc:2PHENDEG-PWY"],"synonyms":[{"name":"phenylethylamine breakdown","type":"exact"},{"name":"phenylethylamine catabolism","type":"exact"},{"name":"phenylethylamine degradation","type":"exact"}],"termid":"GO:0019607"}


id: MONDO:1011085
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis that occurs in goat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urolithiasis, goat","secondary_identifiers":["OMIA:001033-9925"],"termid":"MONDO:1011085","xrefs":{"Monarch":{"xref_id":"1011085"}}}


id: PBO:0089003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar phytochelatin and glutathione S-conjugate ABC family transmembrane transporter Abc2","termid":"PBO:0089003"}


id: PBO:0117148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TSPAN16 antisense RNA 1","termid":"PBO:0117148"}


id: PBO:0050741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family E (Hsp10) member 1 pseudogene 3","termid":"PBO:0050741"}


id: PBO:0063555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paternally expressed 13","termid":"PBO:0063555"}


id: PBO:0084915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitotic spindle protein; interacts with components of the Dam1 (DASH) complex, its effector Sli15p, and microtubule-associated protein Bim1p; also localizes to nuclear microtubules and to the bud neck in a ring-shaped structure; inhibits dynein function","termid":"PBO:0084915"}


id: PBO:0004097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exonuclease I Exo1","termid":"PBO:0004097"}


id: GO:0045600
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of adipocyte differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of fat cell differentiation","termid":"GO:0045598"},{"relation_name":"positively_regulates","term_name":"fat cell differentiation","termid":"GO:0045444"}],"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 fat cell differentiation","synonyms":[{"name":"activation of fat cell differentiation","type":"narrow"},{"name":"positive regulation of adipocyte cell differentiation","type":"exact"},{"name":"positive regulation of adipocyte differentiation","type":"exact"},{"name":"stimulation of fat cell differentiation","type":"narrow"},{"name":"up regulation of fat cell differentiation","type":"exact"},{"name":"up-regulation of fat cell differentiation","type":"exact"},{"name":"upregulation of fat cell differentiation","type":"exact"}],"termid":"GO:0045600"}


id: PBO:0046103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4B pseudogene 6","termid":"PBO:0046103"}


id: MONDO:0019694
data:
  {"annotated_genes":["SJAG_00339","SJAG_00373","SJAG_01216","SJAG_02463","SJAG_04528","SJAG_01941"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008701"},{"annotations":[87115,87116],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010966"},{"annotations":[88217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013223"},{"annotations":[88839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010013"},{"annotations":[87067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009593"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00339":null,"SJAG_00373":null,"SJAG_01216":null,"SJAG_01941":null,"SJAG_02463":null,"SJAG_04528":null},"genotype_count":0,"is_obsolete":false,"name":"spondylodysplastic dysplasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:19193","MEDGEN:1843363","icd11.foundation:329165933","Orphanet:93434","UMLS:C4736216"],"termid":"MONDO:0019694","terms_by_termid":{"MONDO:0008701":null,"MONDO:0009593":null,"MONDO:0010013":null,"MONDO:0010966":null,"MONDO:0013223":null},"xrefs":{"Monarch":{"xref_id":"0019694"}}}


id: MONDO:0005077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A contagious bacterial respiratory infection caused by Bordetella pertussis. It is characterized by severe and uncontrollable cough, resulting in a whooping sound during breathing following the cough.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"commensal bacterial infectious disease","termid":"MONDO:0000315"},{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"bordetellosis","termid":"MONDO:0037872"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pertussis","secondary_identifiers":["GARD:8692","ICD9:033.9","MEDGEN:12159","NCIT:C85231","SCTID:27836007","Orphanet:1489","MESH:D014917","ICD9:033","MedDRA:10047974","ICD10CM:A37.1","EFO:0000650","MedDRA:10034738","ICD9:033.0","NORD:1569","UMLS:C0043167","DOID:1116"],"synonyms":[{"name":"Bordetella infection","type":"broad"},{"name":"Bordetella pertussis caused disease or disorder","type":"exact"},{"name":"Bordetella pertussis disease or disorder","type":"exact"},{"name":"Bordetella pertussis infection","type":"exact"},{"name":"Bordetella pertussis infectious disease","type":"exact"},{"name":"WC - whooping cough","type":"exact"},{"name":"infection due to Bordetella pertussis","type":"related"},{"name":"pertussis","type":"exact"},{"name":"whooping cough","type":"exact"}],"termid":"MONDO:0005077","xrefs":{"Monarch":{"xref_id":"0005077"}}}


id: GO:0035897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the hydrolysis of proteins in another organism by cleavage of their peptide bonds.","definition_xrefs":["GOC:fj","PMID:15922779","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete proteolysis in other organism (obsolete GO:0035897)","termid":"GO:0035897"}


id: MONDO:0009811
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":"osteoma of middle ear","secondary_identifiers":["MESH:C564917","UMLS:C1850142","MEDGEN:342425","OMIM:259650"],"synonyms":[{"name":"osteoma of middle ear","type":"exact"}],"termid":"MONDO:0009811","xrefs":{"Monarch":{"xref_id":"0009811"}}}


id: SO:0002182
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that encodes an antisense long, non-coding RNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"lncRNA_gene","termid":"SO:0002127"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"antisense_lncRNA_gene","synonyms":[{"name":"antisense lncRNA gene","type":"exact"}],"termid":"SO:0002182"}


id: PBO:0052426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KISS1 receptor","termid":"PBO:0052426"}


id: PATO:0001863
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A duration quality of a process inhering in a bearer by virtue of the bearer's having slow progressive course of indefinite duration.","definition_xrefs":["PATOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"duration","termid":"PATO:0001309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic","termid":"PATO:0001863"}


id: GO:2000303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a ceramide biosynthetic process.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amide metabolic process","termid":"GO:0034248"},{"relation_name":"is_a","term_name":"regulation of sphingolipid biosynthetic process","termid":"GO:0090153"},{"relation_name":"regulates","term_name":"ceramide biosynthetic process","termid":"GO:0046513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044085"],"is_obsolete":false,"name":"regulation of ceramide biosynthetic process","synonyms":[{"name":"regulation of ceramide anabolism","type":"exact"},{"name":"regulation of ceramide biosynthesis","type":"exact"},{"name":"regulation of ceramide formation","type":"exact"},{"name":"regulation of ceramide synthesis","type":"exact"}],"termid":"GO:2000303"}


id: GO:0018956
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of phenanthrene, a tricyclic aromatic hydrocarbon, where trans-9(R),10(R)-dihydrodiolphenanthrene is the principal intermediate metabolite.","definition_xrefs":["UM-BBD_pathwayID:pha3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenanthrene catabolic process","termid":"GO:0042216"}],"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":"phenanthrene catabolic process via trans-9(R),10(R)-dihydrodiolphenanthrene","synonyms":[{"name":"phenanthrene breakdown via trans-9(R),10(R)-dihydrodiolphenanthrene","type":"exact"},{"name":"phenanthrene degradation via trans-9(R),10(R)-dihydrodiolphenanthrene","type":"exact"}],"termid":"GO:0018956"}


id: GO:0004107
data:
  {"annotated_genes":["SJAG_03485"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74609],"is_not":false,"summary":null,"term":"GO:0004107"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-O-(1-carboxyvinyl)-3-phosphoshikimate = chorismate + phosphate.","definition_xrefs":["RHEA:21020","EC:4.2.3.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03485":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"chorismate synthase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R01714","MetaCyc:CHORISMATE-SYNTHASE-RXN"],"synonyms":[{"name":"5-O-(1-carboxyvinyl)-3-phosphoshikimate phosphate-lyase (chorismate-forming)","type":"related"},{"name":"5-O-(1-carboxyvinyl)-3-phosphoshikimate phosphate-lyase activity","type":"related"},{"name":"5-enolpyruvylshikimate-3-phosphate phospholyase activity","type":"related"}],"termid":"GO:0004107","terms_by_termid":{"GO:0004107":null}}


id: FYPO:0009072
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population phenotype in which cell growth is increased relative to normal in a medium containing lysine as the nitrogen source.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000139","FYPO:0002058","FYPO:0000003","FYPO:0005447","FYPO:0002057"],"is_obsolete":false,"name":"increased cell population growth on lysine nitrogen source","synonyms":[{"name":"increased growth on lysine nitrogen source","type":"broad"},{"name":"increased vegetative cell growth on lysine nitrogen source","type":"exact"}],"termid":"FYPO:0009072"}


id: PBO:0078814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trophinin","termid":"PBO:0078814"}


id: PBO:0091798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-Pro dipeptidase","termid":"PBO:0091798"}


id: MONDO:0008493
data:
  {"annotated_genes":["SJAG_04731"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88324],"is_not":false,"summary":null,"term":"MONDO:0008493"}]},"cv_name":"mondo","definition":"Overhydrated hereditary stomatocytosis (OHSt) is a disorder of red cell membrane permeability to monovalent cations and is characterized clinically by hemolytic anemia.","definition_xrefs":["Orphanet:3203"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hemolytic anemia","termid":"MONDO:0003689"},{"relation_name":"is_a","term_name":"hereditary stomatocytosis","termid":"MONDO:0020102"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04731":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"overhydrated hereditary stomatocytosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111562","icd11.foundation:595647587","SCTID:722125003","GARD:4183","MESH:C566111","UMLS:C1861455","OMIM:185000","MEDGEN:348876"],"synonyms":[{"name":"OHS","type":"related"},{"name":"OHST","type":"related"},{"name":"OVERHYDRATED hereditary stomatocytosis","type":"related"},{"name":"Potassium sodium disorder of erythrocyte","type":"related"},{"name":"Potassium-sodium disorder of erythrocyte","type":"related"},{"name":"overhydrated hereditary stomatocytosis","type":"exact"},{"name":"stomatocytosis 1","type":"related"},{"name":"stomatocytosis I","type":"related"}],"termid":"MONDO:0008493","terms_by_termid":{"MONDO:0008493":null},"xrefs":{"Monarch":{"xref_id":"0008493"}}}


id: GO:0097228
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The segment of the sperm flagellum where the mitochondrial sheath ends, and the outer dense fibers (ODFs) associated with outer axonemal doublets 3 and 8 are replaced by the 2 longitudinal columns of the fibrous sheath (FS) which run the length of the principal piece and are stabilized by circumferential ribs. The principal piece makes up ~2/3 of the length of the sperm flagellum and is defined by the presence of the FS and of only 7 (rather than 9) ODFs which taper and then terminate near the distal end of the principal piece.","definition_xrefs":["GOC:cjm","MP:0009836"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"sperm flagellum","termid":"GO:0036126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"sperm principal piece","termid":"GO:0097228"}


id: PBO:0070030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1327, pseudogene","termid":"PBO:0070030"}


id: PBO:0002806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-coding RNA, poly(A) bearing (predicted)","termid":"PBO:0002806"}


id: CHEBI:16236
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":"ethanol","termid":"CHEBI:16236"}


id: PBO:0065519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pentatricopeptide repeat domain 1","termid":"PBO:0065519"}


id: PBO:0111860
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calponin homology (CH) domain","termid":"PBO:0111860"}


id: GO:0035599
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the methylthiolation (-SCH3 addition) of the beta-carbon of peptidyl-aspartic acid to form peptidyl-L-beta-methylthioaspartic acid.","definition_xrefs":["PMID:18252828","PMID:8844851","RESID:AA0232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylthiotransferase activity","termid":"GO:0035596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016782","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"aspartic acid methylthiotransferase activity","termid":"GO:0035599"}


id: SO:1000076
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Mutation affects the process of transcription, its initiation, progression or termination.","definition_xrefs":["EBI:www.ebi.ac.uk/mutations/recommendations/mutevent.html"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000076 sequence_variant_affecting_transcription (obsolete SO:1000076)","synonyms":[{"name":"mutation affecting transcription","type":"related"},{"name":"sequence variant affecting transcription","type":"exact"}],"termid":"SO:1000076"}


id: PBO:0110985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cis-acting regulatory lncRNA nam1, byr2 repressing","termid":"PBO:0110985"}


id: PBO:0055050
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 2465","termid":"PBO:0055050"}


id: PBO:0064556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)","termid":"PBO:0064556"}


id: GO:0036523
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a symbiont activates, maintains or increases the frequency, rate or extent of cytokine production by the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:bf","GOC:PARL","PMID:25063865"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by symbiont of host cytokine production (obsolete GO:0036523)","synonyms":[{"name":"'induction by symbiont of host cytokine secretion'","type":"narrow"},{"name":"induction by symbiont of host cytokine secretion","type":"related"},{"name":"positive regulation by symbiont of host cytokine secretion","type":"narrow"}],"termid":"GO:0036523"}


id: PBO:0065951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD17 pseudogene 2","termid":"PBO:0065951"}


id: PBO:0029143
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_kinase_activity","termid":"PBO:0029143"}


id: PBO:0061301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neural proliferation, differentiation and control 1","termid":"PBO:0061301"}


id: PBO:0045749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EBP like","termid":"PBO:0045749"}


id: PBO:0114537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial DUF3818 and PXA domain conserved fungal protein, potential lipid transport protein implicated in membrane organization, ergosterol distribution","termid":"PBO:0114537"}


id: FYECO:0000166
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which sodium chloride (NaCl) was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ NaCl","synonyms":[{"name":"sodium chloride added","type":"exact"}],"termid":"FYECO:0000166"}


id: MONDO:0859577
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"LADD syndrome","termid":"MONDO:0007872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"lacrimoauriculodentodigital syndrome 2","secondary_identifiers":["UMLS:C5774286","DOID:0081371","MEDGEN:1824059","OMIM:620192"],"termid":"MONDO:0859577","xrefs":{"Monarch":{"xref_id":"0859577"}}}


id: PBO:0057511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 629","termid":"PBO:0057511"}


id: GO:0150144
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of CD80 biosynthetic process.","definition_xrefs":["GOC:aruk","PMID:26936882"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of CD80 production (obsolete GO:0150144)","synonyms":[{"name":"negative regulation of CD80 biosynthetic process","type":"exact"}],"termid":"GO:0150144"}


id: PBO:0086452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative membrane glycoprotein; has strong similarity to Vth2p and Pep1p/Vps10p; may be involved in vacuolar protein sorting","termid":"PBO:0086452"}


id: PBO:0062390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 11 pseudogene","termid":"PBO:0062390"}


id: GO:0047568
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 3-oxo-5-beta-steroid + acceptor = a 3-oxo-D4-steroid + reduced acceptor.","definition_xrefs":["EC:1.3.99.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid dehydrogenase activity, acting on the CH-CH group of donors","termid":"GO:0033765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"3-oxo-5-beta-steroid 4-dehydrogenase activity","secondary_identifiers":["RHEA:24172","MetaCyc:3-OXO-5-BETA-STEROID-4-DEHYDROGENASE-RXN"],"synonyms":[{"name":"3-oxo-5beta-steroid 4-dehydrogenase activity","type":"related"},{"name":"3-oxo-5beta-steroid:(acceptor) delta4-oxidoreductase activity","type":"related"},{"name":"3-oxo-5beta-steroid:acceptor delta4-oxidoreductase activity","type":"related"},{"name":"delta4-3-ketosteroid 5-beta-reductase activity","type":"related"}],"termid":"GO:0047568"}


id: PBO:0055065
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 2481","termid":"PBO:0055065"}


id: PBO:0048531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gem nuclear organelle associated protein 7","termid":"PBO:0048531"}


id: PBO:0119877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial respiratory chain complex III assembly protein Cbp4","termid":"PBO:0119877"}


id: PBO:0058246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4534","termid":"PBO:0058246"}


id: GO:0047683
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an aromatic aldehyde + NADP+ + AMP + diphosphate + H2O = an aromatic acid + NADPH + ATP.","definition_xrefs":["RHEA:19229"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde dehydrogenase (NADP+) activity","termid":"GO:0033721"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"aryl-aldehyde dehydrogenase (NADP+) activity","secondary_identifiers":["EC:1.2.1.30","MetaCyc:1.2.1.30-RXN"],"synonyms":[{"name":"aromatic acid reductase activity","type":"related"},{"name":"aryl-aldehyde:NADP+ oxidoreductase (ATP-forming)","type":"related"}],"termid":"GO:0047683"}


id: PBO:0087294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Single stranded DNA-binding protein found at TG1-3 telomere G-tails; key roles in regulation of telomerase, telomere end protection, conventional telomere replication; regulates telomere replication through recruitment of specific sub-complexes, essential function is telomere capping; forms homodimer via N-terminus; disruption of dimerization leads to short telomeres; autophagy and proteasome are involved in Cdc13p degradation; differentially phosphorylated through cell cycle","termid":"PBO:0087294"}


id: GO:0090334
data:
  {"annotated_genes":["SJAG_04771","SJAG_04668","SJAG_01787","SJAG_01255","SJAG_00610","SJAG_04462","SJAG_04666","SJAG_04659","SJAG_03705"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69566,92717,94352,107309,107880,119910,120043],"is_not":false,"summary":null,"term":"GO:0090334"},{"annotations":[89457,94368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of the chemical reactions and pathways resulting in the formation of (1->3)-beta-D-glucans, compounds composed of glucose residues linked by (1->3)-beta-D-glucosidic bonds, found in the walls of cells.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell wall macromolecule metabolic process","termid":"GO:0010981"},{"relation_name":"is_a","term_name":"regulation of (1->3)-beta-D-glucan biosynthetic process","termid":"GO:0032953"},{"relation_name":"is_a","term_name":"regulation of cell wall organization or biogenesis","termid":"GO:1903338"},{"relation_name":"regulates","term_name":"cell wall (1->3)-beta-D-glucan biosynthetic process","termid":"GO:0034411"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01255":null,"SJAG_01787":null,"SJAG_03705":null,"SJAG_04462":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0071554"],"is_obsolete":false,"name":"regulation of cell wall (1->3)-beta-D-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"regulation of cell wall 1,3-beta-D-glucan biosynthetic process","type":"broad"},{"name":"regulation of cell wall 1,3-beta-glucan biosynthetic process","type":"broad"}],"termid":"GO:0090334","terms_by_termid":{"GO:0090334":null,"GO:0140748":null}}


id: GO:0003203
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the endocardial cushion is generated and organized. The endocardial cushion is a specialized region of mesenchymal cells that will give rise to the heart septa and valves.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesenchyme morphogenesis","termid":"GO:0072132"},{"relation_name":"part_of","term_name":"heart morphogenesis","termid":"GO:0003007"},{"relation_name":"part_of","term_name":"endocardial cushion development","termid":"GO:0003197"}],"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":"endocardial cushion morphogenesis","termid":"GO:0003203"}


id: PBO:0069642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 919, pseudogene","termid":"PBO:0069642"}


id: GO:0021710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which neuroblasts acquire specialized structural and/or functional features that characterize the mature cerebellar stellate cell. Differentiation includes the processes involved in commitment of a neuroblast to a cerebellar stellate cell fate. A cerebellar stellate cell is an inhibitory GABAergic interneuron found in the cerebellar cortex.","definition_xrefs":["GOC:jid","GO_REF:0000021","GOC:dph","GOC:cls","GOC:dgh","PMID:15157725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation in hindbrain","termid":"GO:0021533"},{"relation_name":"is_a","term_name":"central nervous system neuron differentiation","termid":"GO:0021953"},{"relation_name":"part_of","term_name":"cerebellar molecular layer formation","termid":"GO:0021688"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebellar stellate cell differentiation","termid":"GO:0021710"}


id: PBO:0063596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal biogenesis factor 11 alpha","termid":"PBO:0063596"}


id: MONDO:0010796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Parkinson disease","termid":"MONDO:0005180"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Parkinson disease, mitochondrial","secondary_identifiers":["OMIM:556500","UMLS:C1838867","MEDGEN:333199","MESH:C564015"],"synonyms":[{"name":"Parkinson disease, mitochondrial","type":"exact"}],"termid":"MONDO:0010796","xrefs":{"Monarch":{"xref_id":"0010796"}}}


id: MONDO:0200000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare adenosarcoma that arises from the uterine ligament.","definition_xrefs":["NCIT:C102570"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical adenosarcoma","termid":"MONDO:0002876"},{"relation_name":"is_a","term_name":"uterine ligament cancer","termid":"MONDO:0003612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"uterine ligament adenosarcoma","synonyms":[{"name":"adenosarcoma of uterine ligament","type":"exact"},{"name":"uterine ligament adenosarcoma","type":"exact"}],"termid":"MONDO:0200000","xrefs":{"Monarch":{"xref_id":"0200000"}}}


id: MONDO:0018261
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"NEVADA (Nevus Epidermicus Verrucosus with AngioDysplasia and Aneurysms) syndrome is a rare, life-threatening, cutaneous disease characterized by a keratinocytic epidermal nevus presenting thick, hystrix-like, white or brownish hyperkeratosis associated with multiple extracutaneous vascular malformations, including angiodysplasia that involves large-vessel arteriovenous shunts that may be fatal during the neonatal period.","definition_xrefs":["Orphanet:370059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"}],"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":"Nevada syndrome","secondary_identifiers":["MEDGEN:1667994","GARD:21593","UMLS:C4751431"],"synonyms":[{"name":"Nevus epidermicus verrucosus with angiodysplasia and aneurysms","type":"exact"}],"termid":"MONDO:0018261","xrefs":{"Monarch":{"xref_id":"0018261"}}}


id: MONDO:0800491
data:
  {"annotated_genes":["SJAG_00760"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012245"}]},"cv_name":"mondo","definition":"A neonatal/infantile epilepsy syndrome characterized by frequent drug-resistant seizures that begin ≤3 months of age, with abnormal interictal EEG and neurological examination. In up to 80% of patients, EIDEE is caused by an underlying structural, genetic, or metabolic reason.","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100620"},{"relation_name":"is_a","term_name":"neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy","termid":"MONDO:0800490"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00760":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"early-infantile DEE","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C116593","Orphanet:1934","SCTID:44423001","MedDRA:10071545","Orphanet:1935","SCTID:230429005","icd11.foundation:1877241469","SCTID:28055006","DOID:2481","DOID:308","DOID:0050709","ICD9:345.6"],"synonyms":[{"name":"EIDEE","type":"exact"},{"name":"EIEE","type":"exact"},{"name":"EME","type":"exact"},{"name":"Ohtahara syndrome","type":"exact"},{"name":"early infantile epileptic encephalopathy","type":"exact"},{"name":"early infantile epileptic encephalopathy with burst-suppression","type":"exact"},{"name":"early infantile epileptic encephalopathy with suppression-bursts","type":"exact"},{"name":"early myoclonic encephalopathy","type":"exact"},{"name":"early myoclonic encephalopathy with suppression-bursts","type":"exact"},{"name":"early-infantile developmental and epileptic encephalopathy syndrome","type":"exact"},{"name":"epileptic encephalopathy, early infantile","type":"exact"},{"name":"epileptic encephalopathy, infantile","type":"exact"},{"name":"epileptic seizures - myoclonic","type":"broad"},{"name":"epileptic seizures, myoclonic","type":"broad"},{"name":"infantile epileptic encephalopathy","type":"exact"},{"name":"myoclonia epileptica","type":"broad"},{"name":"myoclonic epilepsy","type":"broad"},{"name":"myoclonic seizure","type":"broad"},{"name":"myoclonic seizure disorder","type":"broad"},{"name":"myoclonus epilepsy","type":"related"}],"termid":"MONDO:0800491","terms_by_termid":{"MONDO:0012245":null},"xrefs":{"Monarch":{"xref_id":"0800491"}}}


id: FYPO:0004265
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the cortical microtubule cytoskeleton is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton","termid":"FYPO:0004090"},{"relation_name":"is_a","term_name":"abnormal protein localization to cell cortex","termid":"FYPO:0006867"}],"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"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein localization to cortical microtubule cytoskeleton","synonyms":[{"name":"abnormal protein localisation to cortical microtubule cytoskeleton","type":"exact"}],"termid":"FYPO:0004265"}


id: PBO:0047257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 241 member B","termid":"PBO:0047257"}


id: GO:0060763
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The morphogenetic growth of the large, club-shaped terminal end of a mammary gland duct during prepubertal growth and during puberty.","definition_xrefs":["PMID:10804170","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental growth involved in morphogenesis","termid":"GO:0060560"},{"relation_name":"part_of","term_name":"mammary gland duct morphogenesis","termid":"GO:0060603"}],"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":"mammary duct terminal end bud growth","termid":"GO:0060763"}


id: MONDO:0010779
data:
  {"annotated_genes":["SJAG_MIT04"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87852],"is_not":false,"summary":null,"term":"MONDO:0010779"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"prelingual non-syndromic genetic hearing loss","termid":"MONDO:0016297"},{"relation_name":"excluded_subClassOf","term_name":"postlingual non-syndromic genetic hearing loss","termid":"MONDO:0016298"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"}],"gene_count":1,"genes_by_uniquename":{"SJAG_MIT04":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial non-syndromic sensorineural hearing loss","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:90641","MEDGEN:463247","DOID:0111751","GARD:16792","OMIM:500008","UMLS:C3151897"],"synonyms":[{"name":"deafness, isolated, due to mitochondrial transmission","type":"narrow"},{"name":"deafness, nonsyndromic sensorineural, mitochondrial","type":"related"},{"name":"isolated mitochondrial neurosensory deafness","type":"narrow"},{"name":"isolated mitochondrial sensorineural deafness","type":"narrow"},{"name":"mitochondrial non-syndromic neurosensory deafness","type":"narrow"},{"name":"mitochondrial non-syndromic sensorineural deafness","type":"narrow"}],"termid":"MONDO:0010779","terms_by_termid":{"MONDO:0010779":null},"xrefs":{"Monarch":{"xref_id":"0010779"}}}


id: PBO:0077172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tolloid like 1","termid":"PBO:0077172"}


id: GO:1900450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glutamate receptor signaling pathway.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of glutamate receptor signaling pathway","termid":"GO:1900449"},{"relation_name":"negatively_regulates","term_name":"glutamate receptor signaling pathway","termid":"GO:0007215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of glutamate receptor signaling pathway","synonyms":[{"name":"down regulation of glutamate receptor signaling pathway","type":"exact"},{"name":"down regulation of glutamate signaling pathway","type":"exact"},{"name":"down regulation of glutamate signalling pathway","type":"exact"},{"name":"down-regulation of glutamate receptor signaling pathway","type":"exact"},{"name":"down-regulation of glutamate signaling pathway","type":"exact"},{"name":"down-regulation of glutamate signalling pathway","type":"exact"},{"name":"downregulation of glutamate receptor signaling pathway","type":"exact"},{"name":"downregulation of glutamate signaling pathway","type":"exact"},{"name":"downregulation of glutamate signalling pathway","type":"exact"},{"name":"inhibition of glutamate receptor signaling pathway","type":"narrow"},{"name":"inhibition of glutamate signaling pathway","type":"exact"},{"name":"inhibition of glutamate signalling pathway","type":"exact"},{"name":"negative regulation of glutamate signaling pathway","type":"exact"},{"name":"negative regulation of glutamate signalling pathway","type":"exact"}],"termid":"GO:1900450"}


id: PBO:0078221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 10-2","termid":"PBO:0078221"}


id: PBO:0069596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 873, pseudogene","termid":"PBO:0069596"}


id: PATO:0002459
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's similarity to the appearance of a sepal,","definition_xrefs":["PATOC:JL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sepal-like","termid":"PATO:0002459"}


id: PBO:0027543
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-fragmented_mitochondria","termid":"PBO:0027543"}


id: FYPO:0006759
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which chromosome organization is abnormal during the meiotic cell cycle.","definition_xrefs":["PomBase:mah","GO:0070192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromosome organization","termid":"FYPO:0000641"},{"relation_name":"is_a","term_name":"abnormal meiotic cell cycle process","termid":"FYPO:0002739"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000641","FYPO:0000631"],"is_obsolete":false,"name":"abnormal meiotic chromosome organization","synonyms":[{"name":"abnormal chromosome organization during meiotic cell cycle","type":"exact"},{"name":"abnormal chromosome organization involved in meiotic cell cycle","type":"exact"},{"name":"abnormal meiotic chromosome organisation","type":"exact"}],"termid":"FYPO:0006759"}


id: GO:1902628
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of assembly of a large subunit precursor of preribosome.","definition_xrefs":["GO_REF:0000058","GOC:di","GOC:TermGenie","PMID:22735702"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"regulation of assembly of large subunit precursor of preribosome","termid":"GO:1902627"},{"relation_name":"positively_regulates","term_name":"assembly of large subunit precursor of preribosome","termid":"GO:1902626"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"positively_regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"positive regulation of assembly of large subunit precursor of preribosome","synonyms":[{"name":"activation of 66S preribosome assembly","type":"narrow"},{"name":"activation of 66S preribosome formation","type":"narrow"},{"name":"activation of assembly of large subunit precursor of preribosome","type":"narrow"},{"name":"activation of preribosome, large subunit precursor formation","type":"narrow"},{"name":"positive regulation of 66S preribosome assembly","type":"narrow"},{"name":"positive regulation of 66S preribosome formation","type":"narrow"},{"name":"positive regulation of preribosome, large subunit precursor formation","type":"exact"},{"name":"up regulation of 66S preribosome assembly","type":"narrow"},{"name":"up regulation of 66S preribosome formation","type":"narrow"},{"name":"up regulation of assembly of large subunit precursor of preribosome","type":"exact"},{"name":"up regulation of preribosome, large subunit precursor formation","type":"exact"},{"name":"up-regulation of 66S preribosome assembly","type":"narrow"},{"name":"up-regulation of 66S preribosome formation","type":"narrow"},{"name":"up-regulation of assembly of large subunit precursor of preribosome","type":"exact"},{"name":"up-regulation of preribosome, large subunit precursor formation","type":"exact"},{"name":"upregulation of 66S preribosome assembly","type":"narrow"},{"name":"upregulation of 66S preribosome formation","type":"narrow"},{"name":"upregulation of assembly of large subunit precursor of preribosome","type":"exact"},{"name":"upregulation of preribosome, large subunit precursor formation","type":"exact"}],"termid":"GO:1902628"}


id: PBO:0076953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TGFB2 antisense RNA 1 (head to head)","termid":"PBO:0076953"}


id: GO:0014036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into a neural crest cell in an environment that is neutral with respect to the developmental pathway; upon specification, the cell fate can be reversed.","definition_xrefs":["GOC:dh","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stem cell fate specification","termid":"GO:0048866"},{"relation_name":"part_of","term_name":"neural crest cell fate commitment","termid":"GO:0014034"}],"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":"neural crest cell fate specification","termid":"GO:0014036"}


id: FYPO:0006376
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular metabolism phenotype in which the observed occurrence of protein processing is decreased when the cell is subject to nitrogen starvation.","definition_xrefs":["PMID:25803873","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein processing","termid":"FYPO:0006374"},{"relation_name":"is_a","term_name":"decreased proteolysis","termid":"FYPO:0006527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0006551","FYPO:0002494","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein processing during nitrogen starvation","synonyms":[{"name":"decreased protein cleavage during nitrogen starvation","type":"related"},{"name":"decreased protein maturation by peptide bond cleavage during nitrogen starvation","type":"exact"},{"name":"decreased protein maturation by peptide bond hydrolysis during nitrogen starvation","type":"exact"},{"name":"decreased protein processing during nitrogen depletion","type":"exact"},{"name":"decreased protein processing during nitrogen deprivation","type":"exact"},{"name":"reduced protein processing during nitrogen starvation","type":"exact"}],"termid":"FYPO:0006376"}


id: PBO:0076896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 50","termid":"PBO:0076896"}


id: PBO:0052555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell lectin like receptor F2","termid":"PBO:0052555"}


id: PBO:0114412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific microprotein Tam11","termid":"PBO:0114412"}


id: MONDO:0019905
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 9 syndrome is an autosomal anomaly characterized by variable clinical features, most commonly including developmental delay, some degree of intellectual disability, facial dysmorphism, microcephaly, congenital heart anomalies, and variable genital, limb and skeletal anomalies.","definition_xrefs":["Orphanet:96173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 9 disorder","termid":"MONDO:0700016"},{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 9","secondary_identifiers":["UMLS:C0265430","NORD:962","MEDGEN:539244","MESH:C538022","SCTID:60650002","GARD:1348"],"synonyms":[{"name":"Chromosome 9 Ring","type":"exact"},{"name":"Ring 9","type":"exact"},{"name":"Ring chromosome 9 syndrome","type":"related"},{"name":"Ring chromosome type 9","type":"exact"},{"name":"chromosome 9 ring","type":"related"},{"name":"r9","type":"related"}],"termid":"MONDO:0019905","xrefs":{"Monarch":{"xref_id":"0019905"}}}


id: GO:0097214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of the passage or uptake of molecules by the lysosomal membrane.","definition_xrefs":["PMID:20544854","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lysosomal membrane permeability","termid":"GO:0097213"},{"relation_name":"is_a","term_name":"positive regulation of membrane permeability","termid":"GO:1905710"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"positive regulation of lysosomal membrane permeability","synonyms":[{"name":"positive regulation of lysosome membrane permeability","type":"exact"}],"termid":"GO:0097214"}


id: GO:0070939
data:
  {"annotated_genes":["SJAG_01166","SJAG_04956"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[66455,101976],"is_not":false,"summary":null,"term":"GO:0070939"}]},"cv_name":"cellular_component","definition":"A multisubunit tethering complex, i.e. a protein complex involved in mediating the initial interaction between vesicles and the membranes with which they fuse, that is involved in trafficking from the Golgi apparatus to the ER. In Saccharomyces cerevisiae the Dsl1p complex contains Dsl1p, Tip20p, and Sec39p.","definition_xrefs":["PMID:21550981","GOC:jh","PMID:19151722","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle tethering complex","termid":"GO:0099023"},{"relation_name":"is_a","term_name":"endoplasmic reticulum protein-containing complex","termid":"GO:0140534"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01166":null,"SJAG_04956":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005783","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"Dsl1/NZR complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"CATCHR family complex","type":"broad"},{"name":"Dsl1p complex","type":"exact"},{"name":"NZR complex","type":"exact"}],"termid":"GO:0070939","terms_by_termid":{"GO:0070939":null}}


id: PBO:0079605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2F pseudogene 2","termid":"PBO:0079605"}


id: PBO:0055636
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 3075","termid":"PBO:0055636"}


id: MONDO:0700123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Variants in SMARCC1 cause a novel human syndrome characterized by developmental delay, cerebral ventriculomegaly and aqueductal stenosis, and other associated structural brain and cardiac defects.","direct_ancestors":[{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMARCC1-associated developmental dysgenesis syndrome","synonyms":[{"name":"SMARCC1-related BAFopathy","type":"exact"}],"termid":"MONDO:0700123","xrefs":{"Monarch":{"xref_id":"0700123"}}}


id: GO:0002094
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the transfer of multiple prenyl groups from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete polyprenyltransferase activity (obsolete GO:0002094)","termid":"GO:0002094"}


id: PATO:0001599
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An oriented quality inhering in a bearer by virtue of the bearer's being relocated around an axis.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oriented","termid":"PATO:0000614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rotated","synonyms":[{"name":"rotation","type":"exact"}],"termid":"PATO:0001599"}


id: GO:0090553
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cell projection part that is the apical most portion of a unicellular trichome apex.","definition_xrefs":["GOC:PO_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"unicellular trichome apex","termid":"GO:0090552"}],"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":"unicellular trichome tip","termid":"GO:0090553"}


id: GO:0060153
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process in which a virus interferes with the normal progression through the host cell cycle. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete perturbation by virus of host cell cycle progression (obsolete GO:0060153)","synonyms":[{"name":"modulation by virus of host cell cycle","type":"related"},{"name":"modulation of host cell cycle by virus","type":"exact"},{"name":"regulation by virus of host cell cycle","type":"exact"},{"name":"regulation of host cell cycle by virus","type":"exact"},{"name":"viral process regulating host cell cycle","type":"exact"}],"termid":"GO:0060153"}


id: MONDO:0011951
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the FUS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"},{"relation_name":"is_a","term_name":"frontotemporal dementia with motor neuron disease","termid":"MONDO:0017161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"amyotrophic lateral sclerosis type 6","secondary_identifiers":["UMLS:C2931786","DOID:0060198","GARD:9874","MESH:C567699","OMIM:608030","MEDGEN:419901"],"synonyms":[{"name":"ALS6","type":"exact"},{"name":"FUS amyotrophic lateral sclerosis","type":"exact"},{"name":"amyotrophic lateral sclerosis 6 with or without frontotemporal dementia","type":"related"},{"name":"amyotrophic lateral sclerosis 6, with or without frontotemporal dementia","type":"exact"},{"name":"amyotrophic lateral sclerosis caused by mutation in FUS","type":"exact"},{"name":"autosomal recessive amyotrophic lateral sclerosis 6","type":"exact"}],"termid":"MONDO:0011951","xrefs":{"Monarch":{"xref_id":"0011951"}}}


id: PBO:0049616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 19","termid":"PBO:0049616"}


id: PBO:0081762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 692","termid":"PBO:0081762"}


id: GO:1902749
data:
  {"annotated_genes":["SJAG_00117","SJAG_04671","SJAG_01605","SJAG_02392","SJAG_02576","SJAG_00256","SJAG_03486","SJAG_03592","SJAG_03695","SJAG_01901","SJAG_00216","SJAG_01873","SJAG_01205","SJAG_01118","SJAG_00082","SJAG_06592","SJAG_03073","SJAG_02098","SJAG_00640","SJAG_02723","SJAG_00883","SJAG_03160","SJAG_00214","SJAG_03309","SJAG_03126","SJAG_04287","SJAG_01010","SJAG_02332","SJAG_03602","SJAG_00364","SJAG_03026","SJAG_03927","SJAG_04597","SJAG_01084","SJAG_03067","SJAG_04332","SJAG_03942","SJAG_01000","SJAG_04140","SJAG_05373","SJAG_02342","SJAG_00600","SJAG_01855","SJAG_02266","SJAG_02858","SJAG_03854","SJAG_01076","SJAG_02074","SJAG_01456","SJAG_02771","SJAG_01044","SJAG_00526","SJAG_04280","SJAG_02563","SJAG_01146","SJAG_01837","SJAG_01429","SJAG_02592","SJAG_04486","SJAG_00318","SJAG_01805","SJAG_01680","SJAG_04394"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93377,118056,108585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[102496,96356,103398,91943,118002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044878"},{"annotations":[119281,101307,80812,114029,118802,93378,111299,81402,73009,102497,119108,108588,76791,118058,95912,101141,74220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033314"},{"annotations":[100378,96489,118004,97799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031569"},{"annotations":[113722,119021,103011,91067,60996,67987,108589,77143,61704,93379,111300,62528,101309,81275,74222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007095"},{"annotations":[102957,58988,108620,80470,113428,60894,95164,108983,95508,114474,116466,106457,113810,96315],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010972"},{"annotations":[80472,72579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110031"},{"annotations":[94086,118673,89993,113193,93686,90002,100379,72627,105442,96358,95751,103715,96319,110550,112331,75366,118484,100951,109204],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010971"},{"annotations":[103348,89797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905287"},{"annotations":[75368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110032"},{"annotations":[113960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010389"}]},"cv_name":"biological_process","definition":"Any signaling pathway that modulates the activity of a cell cycle cyclin-dependent protein kinase to modulate the switch from G2 phase to M phase of the cell cycle.","definition_xrefs":["GO_REF:0000058","GOC:jl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle phase transition","termid":"GO:1901987"},{"relation_name":"regulates","term_name":"cell cycle G2/M phase transition","termid":"GO:0044839"}],"gene_count":63,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00117":null,"SJAG_00214":null,"SJAG_00216":null,"SJAG_00256":null,"SJAG_00318":null,"SJAG_00364":null,"SJAG_00526":null,"SJAG_00600":null,"SJAG_00640":null,"SJAG_00883":null,"SJAG_01000":null,"SJAG_01010":null,"SJAG_01044":null,"SJAG_01076":null,"SJAG_01084":null,"SJAG_01118":null,"SJAG_01146":null,"SJAG_01205":null,"SJAG_01429":null,"SJAG_01456":null,"SJAG_01605":null,"SJAG_01680":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_01855":null,"SJAG_01873":null,"SJAG_01901":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02266":null,"SJAG_02332":null,"SJAG_02342":null,"SJAG_02392":null,"SJAG_02563":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02723":null,"SJAG_02771":null,"SJAG_02858":null,"SJAG_03026":null,"SJAG_03067":null,"SJAG_03073":null,"SJAG_03126":null,"SJAG_03160":null,"SJAG_03309":null,"SJAG_03486":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03695":null,"SJAG_03854":null,"SJAG_03927":null,"SJAG_03942":null,"SJAG_04140":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04332":null,"SJAG_04394":null,"SJAG_04486":null,"SJAG_04597":null,"SJAG_04671":null,"SJAG_05373":null,"SJAG_06592":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of cell cycle G2/M phase transition","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-8852276"],"termid":"GO:1902749","terms_by_termid":{"GO:0007095":null,"GO:0010389":null,"GO:0010971":null,"GO:0010972":null,"GO:0031569":null,"GO:0033314":null,"GO:0033315":null,"GO:0044878":null,"GO:0110031":null,"GO:0110032":null,"GO:1905287":null}}


id: PBO:0065481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome activator subunit 2","termid":"PBO:0065481"}


id: PBO:0044099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer/testis antigen family 47 member A7","termid":"PBO:0044099"}


id: PBO:0059262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L28","termid":"PBO:0059262"}


id: PBO:0055494
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 2928","termid":"PBO:0055494"}


id: PBO:0075364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRY-box transcription factor 4","termid":"PBO:0075364"}


id: PBO:0000289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human WDR21 family","termid":"PBO:0000289"}


id: MOD:01105
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-bromobenzyloxycarbonyl","synonyms":[{"name":"BrZ","type":"exact"}],"termid":"MOD:01105"}


id: GO:0002648
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of central tolerance induction.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of tolerance induction","termid":"GO:0002645"},{"relation_name":"is_a","term_name":"regulation of central tolerance induction","termid":"GO:0002646"},{"relation_name":"positively_regulates","term_name":"central tolerance induction","termid":"GO:0002508"}],"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 central tolerance induction","synonyms":[{"name":"activation of central tolerance induction","type":"narrow"},{"name":"stimulation of central tolerance induction","type":"narrow"},{"name":"up regulation of central tolerance induction","type":"exact"},{"name":"up-regulation of central tolerance induction","type":"exact"},{"name":"upregulation of central tolerance induction","type":"exact"}],"termid":"GO:0002648"}


id: PBO:0080093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase like 1","termid":"PBO:0080093"}


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


id: GO:0019085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The first phase of viral transcription that occurs after entry of the virus into the host cell, but prior to viral genome replication. It involves the transcription of genes for non-structural proteins, and for lytic viruses, the early gene products are involved in establishing control over the host cell.","definition_xrefs":["GOC:jh2","GOC:jl","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral transcription","termid":"GO:0019083"}],"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":"early viral transcription","synonyms":[{"name":"immediate early viral mRNA transcription","type":"related"}],"termid":"GO:0019085"}


id: PBO:0078535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 27","termid":"PBO:0078535"}


id: MONDO:0004812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of dacryoadenitis.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dacryoadenitis","termid":"MONDO:0004804"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"acute dacryoadenitis","secondary_identifiers":["ICD9:375.01","SCTID:2589008","ICD10CM:H04.01","MEDGEN:508387","UMLS:C0149505","DOID:952"],"synonyms":[{"name":"dacryoadenitis, acute","type":"exact"}],"termid":"MONDO:0004812","xrefs":{"Monarch":{"xref_id":"0004812"}}}


id: GO:0097248
data:
  {"annotated_genes":["SJAG_00661","SJAG_01017","SJAG_01738"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95970,102137,112853],"is_not":false,"summary":null,"term":"GO:0097248"}]},"cv_name":"biological_process","definition":"A process in which a protein or protein complex is maintained in a specific location in the cell cortex of a cell tip, and is prevented from moving elsewhere. The cell cortex of a cell tip is the region directly beneath the plasma membrane at either end of the longest axis of a cylindrical or elongated cell.","definition_xrefs":["GOC:al","PMID:19646873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of protein location in cell cortex","termid":"GO:0032065"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00661":null,"SJAG_01017":null,"SJAG_01738":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"maintenance of protein location in cell cortex of cell tip","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0097248","terms_by_termid":{"GO:0097248":null}}


id: GO:1900605
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of tensidol A.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"tensidol A metabolic process","termid":"GO:1900603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"tensidol A biosynthetic process","synonyms":[{"name":"tensidol A anabolism","type":"exact"},{"name":"tensidol A biosynthesis","type":"exact"},{"name":"tensidol A formation","type":"exact"},{"name":"tensidol A synthesis","type":"exact"}],"termid":"GO:1900605"}


id: GO:1905042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of epithelium regeneration.","definition_xrefs":["GOC:rph","GO_REF:0000058","GOC:TermGenie","PMID:23221517","GOC:BHF_miRNA","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental growth","termid":"GO:0048640"},{"relation_name":"is_a","term_name":"regulation of epithelium regeneration","termid":"GO:1905041"},{"relation_name":"negatively_regulates","term_name":"epithelium regeneration","termid":"GO:1990399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of epithelium regeneration","synonyms":[{"name":"down regulation of epithelium regeneration","type":"exact"},{"name":"down regulation of regeneration of epithelium","type":"exact"},{"name":"down-regulation of epithelium regeneration","type":"exact"},{"name":"down-regulation of regeneration of epithelium","type":"exact"},{"name":"downregulation of epithelium regeneration","type":"exact"},{"name":"downregulation of regeneration of epithelium","type":"exact"},{"name":"inhibition of epithelium regeneration","type":"narrow"},{"name":"inhibition of regeneration of epithelium","type":"narrow"},{"name":"negative regulation of regeneration of epithelium","type":"exact"}],"termid":"GO:1905042"}


id: GO:0015547
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of nalidixic acid from one side of a membrane to the other. Nalidixic acid is a synthetic antibiotic that interferes with DNA gyrase and inhibits prokaryotic replication.","definition_xrefs":["GOC:curators","PMID:12702699","PubChem_Compound:4221"],"gene_count":0,"genotype_count":0,"name":"obsolete nalidixic acid transmembrane transporter activity (obsolete GO:0015547)","synonyms":[{"name":"carbonyl cyanide m-chlorophenylhydrazone/nalidixic acid/organomercurials:hydrogen antiporter activity","type":"related"},{"name":"nalidixic acid transporter activity","type":"related"}],"termid":"GO:0015547"}


id: GO:0002610
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of plasmacytoid dendritic cell antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of dendritic cell antigen processing and presentation","termid":"GO:0002604"},{"relation_name":"regulates","term_name":"plasmacytoid dendritic cell antigen processing and presentation","termid":"GO:0002470"}],"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 plasmacytoid dendritic cell antigen processing and presentation","termid":"GO:0002610"}


id: FYPO:0007175
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the plasma membrane surrounding the cell division site is abolished during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to plasma membrane at cell division site during vegetative growth","termid":"FYPO:0006936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein localization to plasma membrane at cell division site during mitotic interphase","synonyms":[{"name":"abolished protein localisation to plasma membrane at cell division site during mitotic interphase","type":"exact"},{"name":"abolished protein localization in plasma membrane at cell division site during mitotic interphase","type":"exact"},{"name":"abolished protein localization to cell membrane at cell division site during mitotic interphase","type":"exact"},{"name":"abolished protein localization to plasma membrane at cell division site during interphase during vegetative growth","type":"exact"},{"name":"abolished protein localization to plasma membrane at cell division site during interphase of mitotic cell cycle","type":"exact"},{"name":"protein localization to plasma membrane at cell division site abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0007175"}


id: PBO:0053011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"late endosomal/lysosomal adaptor, MAPK and MTOR activator 1","termid":"PBO:0053011"}


id: GO:1990664
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transcription factor complex formed by two or more subunits of Nkx-2.5. Nkx-2.5 is an evolutionary conserved transcription factor important for the specification and differentiation of cardiomyocytes during heart development. It is also required for spleen development. It binds DNA either as a monomer, or a homodimer, or a heterodimer complex to activate or inhibit expression of genes.","definition_xrefs":["GOC:ame","PMID:22849347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"Nkx-2.5 complex","synonyms":[{"name":"NKX.2-5 homodimer complex","type":"related"},{"name":"NKX2.5 complex","type":"related"},{"name":"NKX2E homodimer complex","type":"related"},{"name":"Nkx-2.5 homodimer complex","type":"narrow"}],"termid":"GO:1990664"}


id: MONDO:0017043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low grade childhood congenital malignant neoplasm arising from the kidney. It is characterized by the presence of fibroblastic cells. The majority of cases occur in the first year of life. Complete excision is usually associated with an excellent prognosis.","definition_xrefs":["NCIT:C6569"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesoblastic nephroma","termid":"MONDO:0003130"},{"relation_name":"is_a","term_name":"embryonal neoplasm","termid":"MONDO:0005564"},{"relation_name":"is_a","term_name":"childhood malignant kidney neoplasm","termid":"MONDO:0036511"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005240"],"is_obsolete":false,"name":"congenital mesoblastic nephroma","secondary_identifiers":["MedDRA:10070665","GARD:1493","Orphanet:2665","DOID:4773","icd11.foundation:2001572901","MEDGEN:232058","UMLS:C1332965","ICDO:8960/1"],"synonyms":[{"name":"CMN","type":"exact"},{"name":"CMn","type":"exact"},{"name":"congenital mesoblastic nephroma","type":"exact"},{"name":"mesoblastic nephroma","type":"broad"},{"name":"stromal nephroma, malignant","type":"exact"}],"termid":"MONDO:0017043","xrefs":{"Monarch":{"xref_id":"0017043"}}}


id: PBO:0050274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 4","termid":"PBO:0050274"}


