# terms

id: PBO:0046012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 1 pseudogene 7","termid":"PBO:0046012"}


id: MONDO:0002781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paralysis of the glossopharyngeal nerve.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glossopharyngeal nerve disorder","termid":"MONDO:0002639"},{"relation_name":"is_a","term_name":"cranial nerve palsy","termid":"MONDO:0002782"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glossopharyngeal nerve paralysis","secondary_identifiers":["NCIT:C27335","UMLS:C5231192","MEDGEN:1696475","DOID:3816"],"synonyms":[{"name":"cranial nerve palsy of glossopharyngeal nerve","type":"exact"},{"name":"glossopharyngeal nerve cranial nerve palsy","type":"exact"}],"termid":"MONDO:0002781","xrefs":{"Monarch":{"xref_id":"0002781"}}}


id: GO:1900537
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of glucose homeostasis.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of glucose homeostasis (obsolete GO:1900537)","synonyms":[{"name":"down regulation of glucose homeostasis","type":"exact"},{"name":"down-regulation of glucose homeostasis","type":"exact"},{"name":"downregulation of glucose homeostasis","type":"exact"},{"name":"inhibition of glucose homeostasis","type":"narrow"},{"name":"negative regulation of glucose homeostasis","type":"exact"}],"termid":"GO:1900537"}


id: MONDO:0019688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sulfation-related bone disorder (obsolete MONDO:0019688)","secondary_identifiers":["Orphanet:93423"],"synonyms":[{"name":"inborn error of sulphation","type":"exact"},{"name":"sulphation disorder","type":"exact"}],"termid":"MONDO:0019688","xrefs":{"Monarch":{"xref_id":"0019688"}}}


id: PBO:0073929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 17 member 2","termid":"PBO:0073929"}


id: GO:1901260
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any peptidyl-lysine hydroxylation that is involved in bacterial-type EF-P lysine modification.","definition_xrefs":["PMID:22706199","GOC:TermGenie","GOC:imk"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-lysine hydroxylation involved in bacterial-type EF-P lysine modification (obsolete GO:1901260)","synonyms":[{"name":"EF-P lysine hydroxylation","type":"related"}],"termid":"GO:1901260"}


id: PBO:0058339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4713","termid":"PBO:0058339"}


id: MONDO:0010949
data:
  {"annotated_genes":["SJAG_03137","SJAG_03072"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85101,85102],"is_not":false,"summary":null,"term":"MONDO:0010949"}]},"cv_name":"mondo","definition":"Autosomal dominant Charcot-Marie-Tooth disease type 2B (CMT2B) is a severe form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2B onset, in the 2nd or 3rd decade, is characterized by ulcerations and infections of feet. Symmetric and distal weakness develops mostly in the legs together with a severe symmetric distal sensory loss, tendon reflexes are only reduced at ankles and foot deformities, including pes cavus or planus and hammer toes, appear in childhood.","definition_xrefs":["Orphanet:99936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03072":null,"SJAG_03137":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease type 2B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1833219","GARD:9192","SCTID:717008005","MESH:C537989","OMIM:600882","DOID:0110159","icd11.foundation:1425224652","MEDGEN:371512"],"synonyms":[{"name":"CMT 2B","type":"related"},{"name":"CMT2B","type":"exact"},{"name":"Charcot Marie Tooth disease type 2B","type":"related"},{"name":"Charcot-Marie-Tooth disease type 2 caused by mutation in RAB7A","type":"exact"},{"name":"Charcot-Marie-Tooth disease, autosomal dominant, type 2B","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2B","type":"related"},{"name":"Charcot-Marie-Tooth disease, neuronal, type 2B","type":"related"},{"name":"Charcot-Marie-Tooth disease, type 2B","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy type 2B","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 2B","type":"related"},{"name":"HMSN IIB","type":"exact"},{"name":"HMSN2B","type":"exact"},{"name":"RAB7A Charcot-Marie-Tooth disease type 2","type":"exact"},{"name":"autosomal dominant Charcot-Marie-Tooth disease type 2B","type":"exact"},{"name":"hereditary motor and sensory neuropathy 2 B (HMSN 2 B)","type":"related"},{"name":"hereditary motor and sensory neuropathy 2B","type":"related"},{"name":"hereditary motor and sensory nueropathy IIB","type":"exact"},{"name":"peripheral sensory neuropathy, autosomal dominant (PSN)","type":"related"}],"termid":"MONDO:0010949","terms_by_termid":{"MONDO:0010949":null},"xrefs":{"Monarch":{"xref_id":"0010949"}}}


id: PBO:0113111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Eisosome core component involved in endocytosis; mitochondria phosphoprotein that localizes to the outer membrane and is involved in maintaining mitochondrial morphology and mitophagy; phosphorylated (T233) upon Pkc1p hyperactivation in a Slt2p MAPK-dependent fashion; null mutant shows activation of Pkc1p/Ypk1p stress resistance pathways; BAR domain family member; protein increases in abundance and relocalizes from the plasma membrane to cytoplasm upon DNA replication stress","termid":"PBO:0113111"}


id: MOD:00068
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a glycine residue to N-myristoylglycine.","definition_xrefs":["PubMed:6436247","RESID:AA0059","OMSSA:80","PubMed:11955007","PubMed:1326520","PubMed:7543369","PubMed:1386601","Unimod:45#G","PubMed:11955008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-myristoylated residue","termid":"MOD:00650"},{"relation_name":"is_a","term_name":"modified glycine residue","termid":"MOD:00908"},{"relation_name":"is_a","term_name":"alpha-amino acylated residue","termid":"MOD:01696"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"N-myristoylglycine","synonyms":[{"name":"(tetradecanoylamino)ethanoic acid","type":"exact"},{"name":"LIPID N-myristoyl glycine","type":"exact"},{"name":"Myristoyl","type":"related"},{"name":"Myristoylation","type":"related"},{"name":"N-(1-oxotetradecyl)glycine","type":"exact"},{"name":"N-(C14:0 aliphatic acyl)glycine","type":"exact"},{"name":"N-myristoyl-glycine","type":"exact"},{"name":"N-myristoylated glycine","type":"exact"},{"name":"N-myristylglycine","type":"exact"},{"name":"N-tetradecanoylglycine","type":"exact"},{"name":"NMyrGly","type":"exact"},{"name":"ntermpepmyristoylationg","type":"exact"}],"termid":"MOD:00068"}


id: MONDO:0016328
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy (obsolete MONDO:0016328)","secondary_identifiers":["Orphanet:217591"],"termid":"MONDO:0016328","xrefs":{"Monarch":{"xref_id":"0016328"}}}


id: GO:0141011
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transposable element silencing mechanism in which mRNAs transcribed from transposons are targeted for degradation by a siRNA.","definition_xrefs":["PMID:36570931"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transposable element silencing by mRNA destabilization","termid":"GO:0141008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0010467","GO:0006325","GO:0016071","GO:0008150"],"is_obsolete":false,"name":"transposable element silencing by siRNA-mediated mRNA destabilization","synonyms":[{"name":"siRNA-mediated post-transcriptional retrotransposon silencing","type":"exact"},{"name":"siRNA-mediated retrotransposon silencing by mRNA destabilization","type":"narrow"}],"termid":"GO:0141011"}


id: PBO:0085843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm in a punctate pattern; non-essential gene; upregulated by and required for tolerance to 4-Methylcyclohexane methanol; induced by treatment with 8-methoxypsoralen and UVA irradiation; contains 10-11 predicted transmembrane domains","termid":"PBO:0085843"}


id: MONDO:1010618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microcephaly that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microcephaly, non-human animal","termid":"MONDO:1010066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microcephaly, sheep","secondary_identifiers":["OMIA:000645-9940"],"termid":"MONDO:1010618","xrefs":{"Monarch":{"xref_id":"1010618"}}}


id: PBO:0090507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, DDB1 and CUL4-associated factor Dca7","termid":"PBO:0090507"}


id: PBO:0001386
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"function depends on recruitment to the spindle pole body","termid":"PBO:0001386"}


id: PBO:0061061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NKAIN1 pseudogene 1","termid":"PBO:0061061"}


id: MONDO:0021301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A adenoma that involves the nipple.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system benign neoplasm","termid":"MONDO:0000652"},{"relation_name":"is_a","term_name":"breast adenoma","termid":"MONDO:0002058"},{"relation_name":"is_a","term_name":"nipple neoplasm","termid":"MONDO:0002482"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenoma of nipple","secondary_identifiers":["ICDO:8506/0","NCIT:C4192","SCTID:302829009","UMLS:C0334378","MEDGEN:137752"],"synonyms":[{"name":"adenoma of the nipple","type":"exact"},{"name":"nipple adenoma","type":"exact"},{"name":"papillomatosis, subareolar duct","type":"exact"},{"name":"subareolar duct papillomatosis","type":"related"}],"termid":"MONDO:0021301","xrefs":{"Monarch":{"xref_id":"0021301"}}}


id: PBO:0072677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rubicon autophagy regulator","termid":"PBO:0072677"}


id: PBO:0090999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial TOM complex TPR repeat subunit Tom70","termid":"PBO:0090999"}


id: GO:0034033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a purine nucleoside bisphosphate, a compound consisting of a purine base linked to a deoxyribose or ribose sugar esterified with one phosphate group attached to each of two different hydroxyl groups on the sugar.","definition_xrefs":["GOC:mah","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside bisphosphate biosynthetic process","termid":"GO:0033866"},{"relation_name":"is_a","term_name":"purine nucleoside bisphosphate metabolic process","termid":"GO:0034032"},{"relation_name":"is_a","term_name":"purine-containing compound biosynthetic process","termid":"GO:0072522"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"purine nucleoside bisphosphate biosynthetic process","synonyms":[{"name":"purine nucleoside bisphosphate anabolism","type":"exact"},{"name":"purine nucleoside bisphosphate biosynthesis","type":"exact"},{"name":"purine nucleoside bisphosphate formation","type":"exact"},{"name":"purine nucleoside bisphosphate synthesis","type":"exact"}],"termid":"GO:0034033"}


id: PBO:0043115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic iron-sulfur assembly component 2A","termid":"PBO:0043115"}


id: PBO:0069461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 726, pseudogene","termid":"PBO:0069461"}


id: PBO:0055204
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 2629","termid":"PBO:0055204"}


id: FYPO:0003709
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell adhesion phenotype in which cells adhere to other cells of compatible mating type less strongly or to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell adhesion","termid":"FYPO:0001872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased agglutination","synonyms":[{"name":"decreased agglutination involved in conjugation with cellular fusion","type":"exact"},{"name":"reduced agglutination","type":"exact"}],"termid":"FYPO:0003709"}


id: PBO:0044861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DAP3 binding cell death enhancer 1","termid":"PBO:0044861"}


id: GO:0035231
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of a cytoneme, a long, thin and polarized actin-based cytoplasmic extension that projects from a cell.","definition_xrefs":["PMID:10675901","PMID:10367889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly involved in morphogenesis","termid":"GO:0010927"},{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection assembly","termid":"GO:0120031"},{"relation_name":"part_of","term_name":"cytoneme morphogenesis","termid":"GO:0003399"}],"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":"cytoneme assembly","synonyms":[{"name":"cytoneme biogenesis","type":"related"}],"termid":"GO:0035231"}


id: GO:1903668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of chemorepellent activity.","definition_xrefs":["PMID:24390142","GO_REF:0000059","GOC:TermGenie","PMID:22711818"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of chemorepellent activity (obsolete GO:1903668)","synonyms":[{"name":"down regulation of chemorepellant activity","type":"exact"},{"name":"down regulation of chemorepellent activity","type":"exact"},{"name":"down-regulation of chemorepellant activity","type":"exact"},{"name":"down-regulation of chemorepellent activity","type":"exact"},{"name":"downregulation of chemorepellant activity","type":"exact"},{"name":"downregulation of chemorepellent activity","type":"exact"},{"name":"inhibition of chemorepellant activity","type":"narrow"},{"name":"inhibition of chemorepellent activity","type":"narrow"},{"name":"negative regulation of chemorepellant activity","type":"exact"}],"termid":"GO:1903668"}


id: GO:0010289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of the pectidic homogalacturonan, characterized by a backbone of (1->4)-linked alpha-D-GalpA residues that can be methyl-esterified at C-6 and carry acetyl groups on O-2 and O-3.","definition_xrefs":["PMID:16540543","PMID:12913136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"homogalacturonan metabolic process","termid":"GO:0010394"},{"relation_name":"is_a","term_name":"cell wall pectin biosynthetic process","termid":"GO:0052325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0005975","GO:0071554"],"is_obsolete":false,"name":"homogalacturonan biosynthetic process","secondary_identifiers":["MetaCyc:PWY-1061"],"termid":"GO:0010289"}


id: PBO:0054962
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 2376","termid":"PBO:0054962"}


id: PR:Q9P7Y3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pkr1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7Y3"],"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":"V-type ATPase assembly factor pkr1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP23A10.02","synonyms":[{"name":"Spom972h-pkr1","type":"exact"}],"termid":"PR:Q9P7Y3"}


id: GO:0051467
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events by which a steroid hormone stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of hormone stimulus","termid":"GO:0009720"},{"relation_name":"is_a","term_name":"response to steroid hormone","termid":"GO:0048545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of steroid hormone stimulus","termid":"GO:0051467"}


id: GO:0120324
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The morphological, biochemical and genetic changes that induce the differentiation of bloodstream form trypomastigotes into procyclic trypomastigotes in some of the Trypanosomatidae species such as Trypanosoma brucei. This process occurs inside the midgut of the tsetse fly vectors in T. brucei.","definition_xrefs":["PMID:10593184","GOC:ach","PMID:1698624","PMID:17997129","PMID:3194362","PMID:3194363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"development of symbiont in host","termid":"GO:0044114"}],"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":"procyclogenesis","termid":"GO:0120324"}


id: MONDO:0033565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited oocyte maturation defect","termid":"MONDO:0014769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"oocyte maturation defect 9","secondary_identifiers":["MEDGEN:1724427","OMIM:619011","GARD:18499","UMLS:C5436599"],"synonyms":[{"name":"OOCYTE MATURATION DEFECT 9","type":"related"},{"name":"OOMD9","type":"related"}],"termid":"MONDO:0033565","xrefs":{"Monarch":{"xref_id":"0033565"}}}


id: SO:0001773
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant where the mutated gene product does not allow for one or more basic functions necessary for survival.","direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_abnormal","termid":"SO:0002218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lethal_variant","synonyms":[{"name":"lethal variant","type":"exact"}],"termid":"SO:0001773"}


id: PR:Q09824
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rep2 gene.","definition_xrefs":["UniProtKB:Q09824","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":"transcriptional activator protein rep2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2F12.11c","synonyms":[{"name":"Spom972h-rep2","type":"exact"}],"termid":"PR:Q09824"}


id: MONDO:0018778
data:
  {"annotated_genes":["SJAG_03081","SJAG_00858","SJAG_00243","SJAG_01190","SJAG_00488","SJAG_04409"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85660],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012012"},{"annotations":[84922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014074"},{"annotations":[86811,86810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013338"},{"annotations":[86648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014467"},{"annotations":[87016],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011675"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary motor and sensory neuropathy","termid":"MONDO:0015358"},{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00243":null,"SJAG_00488":null,"SJAG_00858":null,"SJAG_01190":null,"SJAG_03081":null,"SJAG_04409":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"intermediate Charcot-Marie-Tooth disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:21954","Orphanet:476123","icd11.foundation:1389094589","MEDGEN:1826149","NANDO:1200019","UMLS:C5680108","DOID:0050543"],"synonyms":[{"name":"Charcot-Marie-Tooth disease dominant intermediate","type":"narrow"},{"name":"Charcot-Marie-Tooth disease intermediate type","type":"exact"},{"name":"Charcot-Marie-Tooth disease recessive intermediate","type":"narrow"},{"name":"Intermediate hereditary motor and sensory neuropathy","type":"exact"}],"termid":"MONDO:0018778","terms_by_termid":{"MONDO:0011675":null,"MONDO:0012012":null,"MONDO:0013338":null,"MONDO:0014074":null,"MONDO:0014467":null},"xrefs":{"Monarch":{"xref_id":"0018778"}}}


id: PBO:0090255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L27","termid":"PBO:0090255"}


id: GO:0000765
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 pheromone stimulus that regulates the process of pheromone-induced unidirectional conjugation.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to pheromone","termid":"GO:0019236"},{"relation_name":"regulates","term_name":"pheromone-induced unidirectional conjugation","termid":"GO:0000762"}],"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 pheromone regulating pheromone-induced unidirectional conjugation","synonyms":[{"name":"response to pheromone during pheromone-induced unidirectional","type":"related"}],"termid":"GO:0000765"}


id: PBO:0054165
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 1535","termid":"PBO:0054165"}


id: GO:0031701
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an angiotensin receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"angiotensin receptor binding","synonyms":[{"name":"angiotensin receptor ligand","type":"narrow"}],"termid":"GO:0031701"}


id: PBO:0066973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 276","termid":"PBO:0066973"}


id: PBO:0028409
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_superoxide_dismutase_activity","termid":"PBO:0028409"}


id: GO:0003859
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (3R)-3-hydroxybutanoyl-CoA = (2E)-butenoyl-CoA + H2O.","definition_xrefs":["RHEA:17849","EC:4.2.1.55"],"gene_count":0,"genotype_count":0,"name":"obsolete (3R)-3-hydroxybutyryl-CoA dehydratase activity (obsolete GO:0003859)","synonyms":[{"name":"(3R)-3-hydroxybutanoyl-CoA hydro-lyase (crotonoyl-CoA-forming)","type":"related"},{"name":"(3R)-3-hydroxybutanoyl-CoA hydro-lyase activity","type":"related"},{"name":"3-hydroxybutyryl-CoA dehydratase activity","type":"broad"},{"name":"D-3-hydroxybutyryl coenzyme A dehydratase activity","type":"related"},{"name":"D-3-hydroxybutyryl-CoA dehydratase activity","type":"related"},{"name":"crotonase activity","type":"related"},{"name":"enoyl coenzyme A hydrase (D)","type":"broad"}],"termid":"GO:0003859"}


id: GO:0008776
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + acetate = ADP + acetyl phosphate.","definition_xrefs":["EC:2.7.2.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, carboxyl group as acceptor","termid":"GO:0016774"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"acetate kinase activity","secondary_identifiers":["MetaCyc:ACETATEKIN-RXN","RHEA:11352"],"synonyms":[{"name":"AK activity","type":"related"},{"name":"ATP:acetate phosphotransferase activity","type":"related"},{"name":"AckA","type":"related"},{"name":"acetate kinase (phosphorylating) activity","type":"related"},{"name":"acetic kinase activity","type":"related"},{"name":"acetokinase activity","type":"related"}],"termid":"GO:0008776"}


id: PR:Q9P7G8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A UPF0382 inner membrane protein YgdD that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01977"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UPF0382 membrane protein C1782.12c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1782.12c","secondary_identifiers":["UniProtKB:Q9P7G8"],"synonyms":[{"name":"Spom972h-ygdD","type":"exact"}],"termid":"PR:Q9P7G8"}


id: PBO:0077323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 61","termid":"PBO:0077323"}


id: GO:0030411
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: scytalone = 1,3,8-trihydroxynaphthalene + H2O.","definition_xrefs":["RHEA:24396","EC:4.2.1.94"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"scytalone dehydratase activity","secondary_identifiers":["MetaCyc:SCYTALONE-DEHYDRATASE-RXN","KEGG_REACTION:R02907"],"synonyms":[{"name":"scytalone 7,8-hydro-lyase (1,3,8-trihydroxynaphthalene-forming)","type":"related"},{"name":"scytalone 7,8-hydro-lyase activity","type":"related"}],"termid":"GO:0030411"}


id: PBO:0038416
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-acts_upstream_of_or_within,_negative_effect","termid":"PBO:0038416"}


id: MONDO:0014600
data:
  {"annotated_genes":["SJAG_01836"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85052],"is_not":false,"summary":null,"term":"MONDO:0014600"}]},"cv_name":"mondo","definition":"Any dyskeratosis congenita in which the cause of the disease is a mutation in the PARN gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dyskeratosis congenita","termid":"MONDO:0015780"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01836":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"dyskeratosis congenita, autosomal recessive 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070024","NCIT:C176929","UMLS:C4225356","OMIM:616353","GARD:16095","MEDGEN:905452"],"synonyms":[{"name":"DKCB6","type":"exact"},{"name":"PARN dyskeratosis congenita","type":"exact"},{"name":"autosomal recessive dyskeratosis congenita 6","type":"related"},{"name":"dyskeratosis congenita caused by mutation in PARN","type":"exact"},{"name":"dyskeratosis congenita, autosomal recessive 6","type":"exact"},{"name":"dyskeratosis congenita, autosomal recessive type 6","type":"exact"}],"termid":"MONDO:0014600","terms_by_termid":{"MONDO:0014600":null},"xrefs":{"Monarch":{"xref_id":"0014600"}}}


id: PBO:0043680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coronin 7","termid":"PBO:0043680"}


id: PBO:0029525
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_normal_volume_spheroid_vegetative_cell","termid":"PBO:0029525"}


id: PR:Q92345
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pdc101 gene.","definition_xrefs":["UniProtKB:Q92345","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":"pyruvate decarboxylase C1F8.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F8.07c","synonyms":[{"name":"Spom972h-pdc101","type":"exact"}],"termid":"PR:Q92345"}


id: GO:0015868
data:
  {"annotated_genes":["SJAG_03334","SJAG_00612","SJAG_02050"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015866"},{"annotations":[101113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990554"},{"annotations":[101114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990553"},{"annotations":[58923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140021"},{"annotations":[58922,102607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990544"}]},"cv_name":"biological_process","definition":"The directed movement of a purine ribonucleotide, any compound consisting of a purine ribonucleoside (a purine organic base attached to a ribose sugar) esterified with (ortho)phosphate, into, out of or within a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide transport","termid":"GO:0015865"},{"relation_name":"is_a","term_name":"carbohydrate derivative transport","termid":"GO:1901264"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00612":null,"SJAG_02050":null,"SJAG_03334":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"purine ribonucleotide transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0015868","terms_by_termid":{"GO:0015866":null,"GO:0140021":null,"GO:1990544":null,"GO:1990553":null,"GO:1990554":null}}


id: GO:0033936
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the endohydrolysis of the D-mannuronide linkages of polymannuronate.","definition_xrefs":["EC:3.2.1.121"],"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:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016798","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"polymannuronate hydrolase activity","secondary_identifiers":["MetaCyc:3.2.1.121-RXN"],"synonyms":[{"name":"poly(mannuronide) mannuronohydrolase activity","type":"related"},{"name":"polymannuronic acid polymerase activity","type":"related"}],"termid":"GO:0033936"}


id: SO:0002113
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A lncRNA transcript containing a retained intron.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lncRNA_primary_transcript","termid":"SO:0002035"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lncRNA_with_retained_intron","synonyms":[{"name":"lncRNA with retained intron","type":"exact"},{"name":"lncRNA_retained_intron","type":"exact"}],"termid":"SO:0002113"}


id: MONDO:0030500
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Loeys-Dietz syndrome","termid":"MONDO:0018954"}],"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":"Loeys-Dietz syndrome 6","secondary_identifiers":["DOID:0060964","MEDGEN:1794251","OMIM:619656","UMLS:C5562041"],"synonyms":[{"name":"LDS6","type":"exact"}],"termid":"MONDO:0030500","xrefs":{"Monarch":{"xref_id":"0030500"}}}


id: PBO:0090446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exopolyphosphatase, prune Ppx1","termid":"PBO:0090446"}


id: GO:0097677
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a member of the signal transducers and activators of transcription (STAT) protein family. STATs are, as the name indicates, both signal transducers and transcription factors. STATs are activated by cytokines and some growth factors and thus control important biological processes including cell growth, cell differentiation, apoptosis and immune responses.","definition_xrefs":["GOC:mr","InterPro:IPR001217","PMID:24470978","PMID:21447371"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II-specific DNA-binding transcription factor binding","termid":"GO:0061629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"STAT family protein binding","synonyms":[{"name":"signal transducers and activators of transcription family protein binding","type":"exact"}],"termid":"GO:0097677"}


id: PATO:0001457
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of a process inhering in bearer by virtue of the bearer's disposition to respond to stimulation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality of a process","termid":"PATO:0002062"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sensitivity of a process","synonyms":[{"name":"sensitivity of occurrent","type":"exact"}],"termid":"PATO:0001457"}


id: GO:0009760
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The combination of atmospheric CO2 with a 3-carbon molecule phosphoenol pyruvate (PEP) in the mesophyll cells to make a 4-carbon acid which is immediately converted to malic acid. The malic acid is then passed across to the bundle sheath cells where it is broken down again to pyruvic acid and CO2. The acid is passed back to the mesophyll cells to be used again, while the CO2 is fed into the reductive pentose-phosphate cycle (Calvin cycle) and converted into sugar and starch.","definition_xrefs":["ISBN:0816017360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon fixation","termid":"GO:0015977"},{"relation_name":"is_a","term_name":"photosynthesis, dark reaction","termid":"GO:0019685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"C4 photosynthesis","secondary_identifiers":["Wikipedia:C4_carbon_fixation"],"termid":"GO:0009760"}


id: GO:0007308
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis, deposition, and organization of the materials in a cell of an ovary; where the cell can then undergo meiosis and form an ovum. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mtg_sensu","GOC:tb","GOC:ems","ISBN:0198506732","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"cell maturation","termid":"GO:0048469"},{"relation_name":"part_of","term_name":"oocyte development","termid":"GO:0048599"}],"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":"oocyte construction","secondary_identifiers":["GO:0048110"],"synonyms":[{"name":"oocyte arrangement","type":"exact"}],"termid":"GO:0007308"}


id: FYPO:0007773
data:
  {"alleles_by_uniquename":{"SJAG_00124:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00124","name":"SJAG_00124delta","uniquename":"SJAG_00124:allele-1"},"SJAG_00266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00266","name":"atf1delta","uniquename":"SJAG_00266:allele-1"},"SJAG_00364:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00364","name":"rad3delta","uniquename":"SJAG_00364:allele-1"},"SJAG_00429:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00429","name":"rad26delta","uniquename":"SJAG_00429:allele-1"},"SJAG_00514:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00514","name":"scd1delta","uniquename":"SJAG_00514:allele-1"},"SJAG_00610:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00610","name":"pck2delta","uniquename":"SJAG_00610:allele-1"},"SJAG_01205:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01205","name":"crb2delta","uniquename":"SJAG_01205:allele-1"},"SJAG_01605:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01605","name":"rad9delta","uniquename":"SJAG_01605:allele-1"},"SJAG_01680:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01680","name":"chk1delta","uniquename":"SJAG_01680:allele-1"},"SJAG_01680:allele-2":{"allele_type":"amino_acid_mutation","description":"P470L","gene_uniquename":"SJAG_01680","name":"chk1-P470L","synonyms":[{"name":"chk1- hyperactive (chk1-hyp)","reference":"PMID:23090706","type":"exact"},{"name":"chk1-hyperactive (chk1-hyp)","reference":"PMID:20368354","type":"exact"}],"uniquename":"SJAG_01680:allele-2"},"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"},"SJAG_01794:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01794","name":"scd2delta","uniquename":"SJAG_01794:allele-1"},"SJAG_02013:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02013","name":"pyp1delta","uniquename":"SJAG_02013:allele-1"},"SJAG_02266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02266","name":"rad24delta","uniquename":"SJAG_02266:allele-1"},"SJAG_02379:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02379","name":"gap1delta","uniquename":"SJAG_02379:allele-1"},"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"},"SJAG_02576:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02576","name":"rad25delta","uniquename":"SJAG_02576:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_02771:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02771","name":"rad1delta","uniquename":"SJAG_02771:allele-1"},"SJAG_02819:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02819","name":"efc25delta","uniquename":"SJAG_02819:allele-1"},"SJAG_02923:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02923","name":"spk1delta","uniquename":"SJAG_02923:allele-1"},"SJAG_03453:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03453","name":"ras1delta","uniquename":"SJAG_03453:allele-1"},"SJAG_03720:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03720","name":"tel1delta","uniquename":"SJAG_03720:allele-1"},"SJAG_04312:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04312","name":"pka1delta","uniquename":"SJAG_04312: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"},"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007780"},{"annotations":[119081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007779"}],"single_locus_phenotype":[{"annotations":[118868,118994],"is_not":false,"summary":null,"term":"FYPO:0007773"},{"annotations":[118851,118883,118884,118852,118861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007789"},{"annotations":[119175,119171,119294,119296,119298,119299,119295,119291,119293,119292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007782"},{"annotations":[119077],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007778"},{"annotations":[118898,118914,118919,119266,119092,118922,118910,119076,119079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007776"},{"annotations":[119091,118915,119078,118920,118923,118899,119080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007780"},{"annotations":[119075,119071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007777"},{"annotations":[118903,119074,119070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007775"},{"annotations":[119317,119069,119073,119170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007774"},{"annotations":[118904,119072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007779"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which any aspect of hyphal growth is abnormal.","definition_xrefs":["GO:0030448","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell phenotype","termid":"FYPO:0000002"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00124":null,"SJAG_00266":null,"SJAG_00364":null,"SJAG_00429":null,"SJAG_00514":null,"SJAG_00610":null,"SJAG_01205":null,"SJAG_01605":null,"SJAG_01680":null,"SJAG_01787":null,"SJAG_01794":null,"SJAG_02013":null,"SJAG_02266":null,"SJAG_02379":null,"SJAG_02527":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02771":null,"SJAG_02819":null,"SJAG_02923":null,"SJAG_03453":null,"SJAG_03720":null,"SJAG_04312":null,"SJAG_04551":null,"SJAG_04697":null},"genotype_count":31,"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"}]}]},"SJAG_00124delta":{"display_name":"SJAG_00124delta","display_uniquename":"SJAG_00124delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00124:allele-1","expression":"Null"}]}]},"SJAG_00124delta__sty1delta":{"display_name":"SJAG_00124delta sty1delta","display_uniquename":"SJAG_00124delta__sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00124:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]},"atf1delta":{"display_name":"atf1delta","display_uniquename":"atf1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00266:allele-1","expression":"Null"}]}]},"chk1-P470L-P470L-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"chk1-P470L(aa)","display_uniquename":"chk1-P470L-P470L-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01680:allele-2","expression":"Not assayed or wild type"}]}]},"chk1delta":{"display_name":"chk1delta","display_uniquename":"chk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01680:allele-1","expression":"Null"}]}]},"crb2delta":{"display_name":"crb2delta","display_uniquename":"crb2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01205:allele-1","expression":"Null"}]}]},"efc25delta":{"display_name":"efc25delta","display_uniquename":"efc25delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02819:allele-1","expression":"Null"}]}]},"gap1delta":{"display_name":"gap1delta","display_uniquename":"gap1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02379:allele-1","expression":"Null"}]}]},"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]},"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown":{"display_name":"lig4::KanMX6(RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]},"pck1delta":{"display_name":"pck1delta","display_uniquename":"pck1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]}]},"pck1delta__pmk1delta":{"display_name":"pck1delta pmk1delta","display_uniquename":"pck1delta__pmk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-1","expression":"Null"}]}]},"pck2delta":{"display_name":"pck2delta","display_uniquename":"pck2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00610:allele-1","expression":"Null"}]}]},"pka1delta":{"display_name":"pka1delta","display_uniquename":"pka1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04312:allele-1","expression":"Null"}]}]},"pmk1delta":{"display_name":"pmk1delta","display_uniquename":"pmk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-1","expression":"Null"}]}]},"pyp1delta":{"display_name":"pyp1delta","display_uniquename":"pyp1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02013:allele-1","expression":"Null"}]}]},"rad1delta":{"display_name":"rad1delta","display_uniquename":"rad1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02771:allele-1","expression":"Null"}]}]},"rad24delta":{"display_name":"rad24delta","display_uniquename":"rad24delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02266:allele-1","expression":"Null"}]}]},"rad25delta":{"display_name":"rad25delta","display_uniquename":"rad25delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02576:allele-1","expression":"Null"}]}]},"rad26delta":{"display_name":"rad26delta","display_uniquename":"rad26delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00429:allele-1","expression":"Null"}]}]},"rad3delta":{"display_name":"rad3delta","display_uniquename":"rad3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00364:allele-1","expression":"Null"}]}]},"rad9delta":{"display_name":"rad9delta","display_uniquename":"rad9delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01605:allele-1","expression":"Null"}]}]},"ras1delta":{"display_name":"ras1delta","display_uniquename":"ras1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03453:allele-1","expression":"Null"}]}]},"scd1delta":{"display_name":"scd1delta","display_uniquename":"scd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00514:allele-1","expression":"Null"}]}]},"scd2delta":{"display_name":"scd2delta","display_uniquename":"scd2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01794:allele-1","expression":"Null"}]}]},"spk1delta":{"display_name":"spk1delta","display_uniquename":"spk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02923:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]},"tel1delta":{"display_name":"tel1delta","display_uniquename":"tel1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03720:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_01787","SJAG_02592","SJAG_04551","SJAG_00124"],"name":"abnormal hyphal growth","references_by_uniquename":{"PMID:20368354":null,"PMID:23090706":null,"PMID:27678009":null,"PMID:29566183":null,"PMID:31150379":null,"PMID:34198697":null,"PMID:36058798":null,"PMID:37233261":null},"single_locus_annotated_genes":["SJAG_02592","SJAG_02923","SJAG_02771","SJAG_02576","SJAG_00429","SJAG_01605","SJAG_03453","SJAG_02013","SJAG_01794","SJAG_01787","SJAG_02819","SJAG_03720","SJAG_04697","SJAG_02379","SJAG_04312","SJAG_00514","SJAG_02266","SJAG_01205","SJAG_00364","SJAG_01680","SJAG_02527","SJAG_04551","SJAG_00610","SJAG_00124","SJAG_00266"],"single_locus_genotype_uniquenames":["Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","chk1-P470L-P470L-amino_acid_mutation-expression-not_assayed_or_wild_type","efc25delta","pck1delta","atf1delta","SJAG_00124delta","scd1delta","sty1delta","rad1delta","rad25delta","rad24delta","pck2delta","spk1delta","Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","chk1delta","pmk1delta","crb2delta","pka1delta","gap1delta","gms1delta","tel1delta","rad26delta","Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","rad3delta","rad9delta","pyp1delta","scd2delta","ras1delta"],"termid":"FYPO:0007773","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000314":null,"FYPO:0007773":null,"FYPO:0007774":null,"FYPO:0007775":null,"FYPO:0007776":null,"FYPO:0007777":null,"FYPO:0007778":null,"FYPO:0007779":null,"FYPO:0007780":null,"FYPO:0007782":null,"FYPO:0007789":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null,"FYPO_EXT:0000003":null}}


id: MONDO:0012431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital diaphragmatic hernia in which the cause of the disease is a mutation in the ZFPM2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital diaphragmatic hernia","termid":"MONDO:0005711"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diaphragmatic hernia 3","secondary_identifiers":["OMIM:610187","MESH:C565710","GARD:15474","MEDGEN:347546","UMLS:C1857781"],"synonyms":[{"name":"DIH3","type":"related"},{"name":"ZFPM2 congenital diaphragmatic hernia","type":"exact"},{"name":"congenital diaphragmatic hernia caused by mutation in ZFPM2","type":"exact"},{"name":"diaphragmatic hernia 3","type":"exact"},{"name":"diaphragmatic hernia type 3","type":"exact"}],"termid":"MONDO:0012431","xrefs":{"Monarch":{"xref_id":"0012431"}}}


id: MONDO:0024985
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diseases of domestic and mountain sheep of the genus Ovis.","definition_xrefs":["MESH:D012757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sheep disease","synonyms":[{"name":"Ovine disease","type":"related"},{"name":"Ovine diseases","type":"related"},{"name":"disease, Ovine","type":"related"},{"name":"disease, sheep","type":"related"},{"name":"diseases, Ovine","type":"related"},{"name":"diseases, sheep","type":"related"},{"name":"sheep disease","type":"exact"}],"termid":"MONDO:0024985","xrefs":{"Monarch":{"xref_id":"0024985"}}}


id: PBO:0065278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich coiled-coil 2B","termid":"PBO:0065278"}


id: GO:0001828
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The morphogenesis of cells in the inner cell mass.","definition_xrefs":["ISBN:0198542771","GOC:dph","ISBN:0124020607"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"inner cell mass cell differentiation","termid":"GO:0001826"}],"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":"inner cell mass cellular morphogenesis","termid":"GO:0001828"}


id: PBO:0111428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex subunit Exo5-like, F-box protein Pof6","termid":"PBO:0111428"}


id: MOD:01289
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other -","definition_xrefs":["Unimod:255#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetaldehyde +28","termid":"MOD:00578"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetaldehyde +28 - site K","synonyms":[{"name":"Acetaldehyde +28","type":"related"},{"name":"Delta:H(4)C(2)","type":"related"}],"termid":"MOD:01289"}


id: MONDO:0024355
data:
  {"annotated_genes":["SJAG_05979"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800029"}]},"cv_name":"mondo","definition":"Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases.","definition_xrefs":["MESH:D012141"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"infectious disease","termid":"MONDO:0005550"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05979":null},"genotype_count":0,"is_obsolete":false,"name":"respiratory tract infectious disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:275498002","ICD9:519.8"],"synonyms":[{"name":"infection, respiratory tract","type":"related"},{"name":"infections, respiratory","type":"related"},{"name":"infections, respiratory tract","type":"related"},{"name":"infections, upper respiratory","type":"related"},{"name":"infections, upper respiratory tract","type":"related"},{"name":"respiratory infection, upper","type":"narrow"},{"name":"respiratory infections","type":"related"},{"name":"respiratory tract infection","type":"related"},{"name":"upper respiratory infections","type":"narrow"},{"name":"upper respiratory tract infections","type":"narrow"}],"termid":"MONDO:0024355","terms_by_termid":{"MONDO:0800029":null},"xrefs":{"Monarch":{"xref_id":"0024355"}}}


id: GO:0004134
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a segment of a (1->4)-alpha-D-glucan to a new 4-position in an acceptor, which may be glucose or (1->4)-alpha-D-glucan.","definition_xrefs":["EC:2.4.1.25"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016757","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"4-alpha-glucanotransferase activity","secondary_identifiers":["Reactome:R-HSA-71552"],"synonyms":[{"name":"1,4-alpha-D-glucan:1,4-alpha-D-glucan 4-alpha-D-glycosyltransferase activity","type":"related"},{"name":"D-enzyme activity","type":"related"},{"name":"amylomaltase activity","type":"related"},{"name":"debranching enzyme maltodextrin glycosyltransferase activity","type":"related"},{"name":"dextrin glycosyltransferase activity","type":"related"},{"name":"dextrin transglycosylase activity","type":"related"},{"name":"disproportionating enzyme activity","type":"related"},{"name":"oligo-1,4-1,4-glucantransferase activity","type":"related"}],"termid":"GO:0004134"}


id: PBO:0087134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding protein required for maturation of tRNA and U6 snRNA; acts as a molecular chaperone for RNAs transcribed by polymerase III; homologous to human La (SS-B) autoantigen","termid":"PBO:0087134"}


id: GO:0021908
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals generated as a consequence of a retinoic acid receptor binding to one of its physiological ligands that results in the spatial identity of regions along the anterior-posterior axis of the spinal cord.","definition_xrefs":["PMID:11262869","GOC:dgh","GOC:dph","GOC:cls","GO_REF:0000021","GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete retinoic acid receptor signaling pathway involved in spinal cord anterior/posterior pattern formation (obsolete GO:0021908)","synonyms":[{"name":"retinoic acid receptor signalling pathway in spinal cord anterior-posterior patterning","type":"exact"}],"termid":"GO:0021908"}


id: MONDO:0015785
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Prader-Willi syndrome","termid":"MONDO:0008300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0700092"],"is_obsolete":false,"name":"Prader-Willi syndrome due to translocation","secondary_identifiers":["UMLS:C5680509","Orphanet:177907","MEDGEN:1826085","GARD:17074"],"termid":"MONDO:0015785","xrefs":{"Monarch":{"xref_id":"0015785"}}}


id: PBO:0057125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 208b","termid":"PBO:0057125"}


id: PBO:0068254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 45S pre-ribosomal 1","termid":"PBO:0068254"}


id: MONDO:0013787
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":"psychomotor retardation, epilepsy, and craniofacial dysmorphism","secondary_identifiers":["OMIM:614501","UMLS:C3281055","MEDGEN:482685"],"synonyms":[{"name":"PMRED","type":"related"},{"name":"neurodevelopmental disorder with hypotonia, craniofacial abnormalities, and seizures","type":"exact"},{"name":"psychomotor retardation, epilepsy, and craniofacial dysmorphism","type":"exact"}],"termid":"MONDO:0013787","xrefs":{"Monarch":{"xref_id":"0013787"}}}


id: MONDO:0003454
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the conjunctiva.","direct_ancestors":[{"relation_name":"is_a","term_name":"ocular cancer","termid":"MONDO:0002236"},{"relation_name":"is_a","term_name":"conjunctival tumor","termid":"MONDO:0020204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004992"],"is_obsolete":false,"name":"conjunctival cancer","secondary_identifiers":["DOID:5467","NCIT:C3564","ICD9:190.3","MEDGEN:56316","SCTID:363463000","UMLS:C0153628"],"synonyms":[{"name":"cancer of conjunctiva","type":"broad"},{"name":"conjunctiva cancer","type":"exact"},{"name":"conjunctival tumor","type":"broad"},{"name":"conjunctival tumour","type":"broad"},{"name":"malignant conjunctiva neoplasm","type":"exact"},{"name":"malignant conjunctiva tumor","type":"exact"},{"name":"malignant conjunctiva tumour","type":"exact"},{"name":"malignant conjunctival neoplasm","type":"exact"},{"name":"malignant conjunctival tumor","type":"exact"},{"name":"malignant conjunctival tumour","type":"exact"},{"name":"malignant neoplasm of conjunctiva","type":"exact"},{"name":"malignant neoplasm of conjunctiva (primary)","type":"exact"},{"name":"malignant neoplasm of the conjunctiva","type":"exact"},{"name":"malignant tumor of conjunctiva","type":"exact"},{"name":"malignant tumor of the conjunctiva","type":"exact"},{"name":"malignant tumour of conjunctiva","type":"exact"},{"name":"malignant tumour of the conjunctiva","type":"exact"}],"termid":"MONDO:0003454","xrefs":{"Monarch":{"xref_id":"0003454"}}}


id: GO:0016655
data:
  {"annotated_genes":["SJAG_04152","SJAG_02697","SJAG_01539","SJAG_03476"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003955"},{"annotations":[112602],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008137"},{"annotations":[96477,112603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050136"},{"annotations":[74118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003960"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which NADH or NADPH acts as a hydrogen or electron donor and reduces a quinone or a similar acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H","termid":"GO:0016651"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01539":null,"SJAG_02697":null,"SJAG_03476":null,"SJAG_04152":null},"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":"oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:1.6.5.-"],"synonyms":[{"name":"oxidoreductase activity, acting on NADH or NADPH, quinone or similar compound as acceptor","type":"related"}],"termid":"GO:0016655","terms_by_termid":{"GO:0003955":null,"GO:0003960":null,"GO:0008137":null,"GO:0050136":null}}


id: PBO:0091383
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae ILV3","termid":"PBO:0091383"}


id: MONDO:0024677
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An insulin-producing neuroendocrine tumor arising from the beta cells of the pancreas. Patients exhibit symptoms related to hypoglycemia due to inappropriate secretion of insulin.","definition_xrefs":["NCIT:C95598"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic insulin-producing neuroendocrine tumor","termid":"MONDO:0005048"},{"relation_name":"is_a","term_name":"functional pancreatic neuroendocrine tumor","termid":"MONDO:0023206"}],"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":"pancreatic insulinoma","secondary_identifiers":["MedDRA:10022498","NANDO:2200398","HP:0012197","SCTID:302822000","DOID:3892","MEDGEN:43907","MESH:D007340","UMLS:C0021670"],"synonyms":[{"name":"Insulinomas","type":"related"},{"name":"Insulomas","type":"related"},{"name":"adenoma, beta cell","type":"related"},{"name":"adenoma, beta-cell","type":"related"},{"name":"adenomas, beta-cell","type":"related"},{"name":"beta cell tumor","type":"related"},{"name":"beta cell tumour","type":"related"},{"name":"beta-cell adenoma","type":"related"},{"name":"beta-cell adenomas","type":"related"},{"name":"beta-cell tumor","type":"related"},{"name":"beta-cell tumors","type":"related"},{"name":"beta-cell tumour","type":"related"},{"name":"beta-cell tumours","type":"related"},{"name":"insulin-producing tumour of islet cells","type":"related"},{"name":"insulinoma","type":"exact"},{"name":"insulinoma tumor suppressor GENE locus","type":"related"},{"name":"insulinoma tumour suppressor GENE locus","type":"related"},{"name":"insuloma","type":"related"},{"name":"islet cell adenoma","type":"related"},{"name":"pancreatic insulinoma","type":"exact"},{"name":"tumor, beta-cell","type":"related"},{"name":"tumors, beta-cell","type":"related"}],"termid":"MONDO:0024677","xrefs":{"Monarch":{"xref_id":"0024677"}}}


id: MONDO:1010558
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spina bifida that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spina bifida, non-human animal","termid":"MONDO:1010047"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spina bifida, cattle","secondary_identifiers":["OMIA:000933-9913"],"termid":"MONDO:1010558","xrefs":{"Monarch":{"xref_id":"1010558"}}}


id: PBO:0043455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin and CBS domain divalent metal cation transport mediator 1","termid":"PBO:0043455"}


id: SO:0002155
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A genomic region in which there is an exchange of genetic material as a result of the repair of meiosis-specific double strand breaks that occur during meiotic prophase.","definition_xrefs":["NCBI:cf","SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"recombination_feature","termid":"SO:0000298"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic_recombination_region","synonyms":[{"name":"INSDC_feature:misc_recomb","type":"broad"},{"name":"INSDC_qualifier:meiotic","type":"exact"},{"name":"INSDC_qualifier:meiotic_recombination","type":"exact"},{"name":"meiotic recombination region","type":"exact"}],"termid":"SO:0002155"}


id: GO:0004903
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a growth hormone and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:ai","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"growth hormone receptor activity","termid":"GO:0004903"}


id: PBO:0060653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NCOR1 pseudogene 2","termid":"PBO:0060653"}


id: PBO:0016901
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snu2 transcription termination requires hairpin structure cleaved by Pac1","termid":"PBO:0016901"}


id: GO:0030895
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Protein complex that mediates editing of the mRNA encoding apolipoprotein B; catalyzes the deamination of C to U (residue 6666 in the human mRNA). Contains a catalytic subunit, APOBEC-1, and other proteins (e.g. human ASP; rat ASP and KSRP).","definition_xrefs":["PMID:12683974","PMID:10781591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA editing complex","termid":"GO:0045293"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"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":"apolipoprotein B mRNA editing enzyme complex","synonyms":[{"name":"APOBEC","type":"exact"},{"name":"apoB mRNA editing enzyme complex","type":"exact"}],"termid":"GO:0030895"}


id: GO:0072463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about whether spindle is correctly assembled and chromosomes are attached to the spindle is received and converted into a molecular signal, contributing to a meiotic spindle assembly checkpoint.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in meiotic spindle assembly checkpoint (obsolete GO:0072463)","synonyms":[{"name":"meiotic spindle assembly checkpoint sensor mechanism","type":"related"},{"name":"meiotic spindle assembly checkpoint sensor process","type":"related"},{"name":"sensing involved in meiotic spindle assembly checkpoint","type":"related"}],"termid":"GO:0072463"}


id: GO:2001079
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to beta-D-Gal-(1->4)-beta-D-GlcNAc-(1->3)-beta-D-Gal-(1->4)-D-Glc.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate derivative binding","termid":"GO:0097367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"beta-D-Gal-(1->4)-beta-D-GlcNAc-(1->3)-beta-D-Gal-(1->4)-D-Glc binding","termid":"GO:2001079"}


id: PBO:0029870
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K4_dimethylation","termid":"PBO:0029870"}


id: PBO:0085764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase of unknown cellular role; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus; null mutant is sensitive to expression of the top1-T722A allele; not an essential gene; relocalizes from nucleus to cytoplasm upon DNA replication stress","termid":"PBO:0085764"}


id: PBO:0084205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Homeobox transcriptional repressor; binds Mcm1p and early cell cycle box (ECB) elements of cell cycle regulated genes, thereby restricting ECB-mediated transcription to the M/G1 interval; YHP1 has a paralog, YOX1, that arose from the whole genome duplication","termid":"PBO:0084205"}


id: PR:Q9UUF4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC17A3.02 gene.","definition_xrefs":["UniProtKB:Q9UUF4","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":"altered inheritance of mitochondria protein 19 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17A3.02","synonyms":[{"name":"Spom972h-SPBC17A3.02","type":"exact"}],"termid":"PR:Q9UUF4"}


id: MONDO:0002223
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant mesothelial neoplasm that usually involves both the ovarian surface and the ovarian stroma. In most cases there is bilateral ovarian involvement.","definition_xrefs":["NCIT:C40444"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant mesothelioma","termid":"MONDO:0006292"},{"relation_name":"is_a","term_name":"ovarian cancer","termid":"MONDO:0008170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"ovarian malignant mesothelioma","secondary_identifiers":["MEDGEN:274089","UMLS:C1518721","DOID:2143"],"synonyms":[{"name":"malignant mesothelioma (disease) of ovary","type":"exact"},{"name":"ovarian malignant mesothelioma","type":"exact"},{"name":"ovary malignant mesothelioma (disease)","type":"exact"}],"termid":"MONDO:0002223","xrefs":{"Monarch":{"xref_id":"0002223"}}}


id: PBO:0044503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine rich transmembrane module containing 1","termid":"PBO:0044503"}


id: PBO:0063608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosylformylglycinamidine synthase","termid":"PBO:0063608"}


id: PBO:0051634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inner mitochondrial membrane peptidase subunit 2","termid":"PBO:0051634"}


id: GO:0021531
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which neuroepithelial cells in the ventral neural tube acquire specialized structural and/or functional features of radial glial cells. Radial cell precursors differentiate into both neuronal cell types and mature radial glial cells. Mature radial glial cells regulate the axon growth and pathfinding processes that occur during white matter patterning of the developing spinal cord. Differentiation includes the processes involved in commitment of a cell to a specific fate.","definition_xrefs":["GOC:dph","GOC:jid","PMID:16185248","GOC:cls","GO_REF:0000021","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation in spinal cord","termid":"GO:0021515"},{"relation_name":"is_a","term_name":"radial glial cell differentiation","termid":"GO:0060019"}],"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":"spinal cord radial glial cell differentiation","synonyms":[{"name":"radial glial cell differentiation in spinal cord","type":"exact"}],"termid":"GO:0021531"}


id: GO:0075093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism modulates the frequency, rate or extent of the symbiont signal transduction mediated by G-protein beta subunit. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by host of symbiont signal transduction mediated by G-protein beta subunit (obsolete GO:0075093)","termid":"GO:0075093"}


id: PBO:0113754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein Meu18, C2 domain","termid":"PBO:0113754"}


id: PATO:0001106
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001106 relative strain value (obsolete PATO:0001106)","termid":"PATO:0001106"}


id: PBO:0088447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase (CK1 family) Cki1","termid":"PBO:0088447"}


id: PBO:0040709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 like 14","termid":"PBO:0040709"}


id: MONDO:0012396
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Exercise-induced hyperinsulinism (EIHI) is a form of diazoxide-sensitive diffuse hyperinsulinism (DHI) characterized by episodes of hypoglycemia induced by exercise due to an inappropriate lactate and pyruvate sensitivity in pancreatic beta-cells.","definition_xrefs":["Orphanet:165991"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diazoxide-sensitive diffuse hyperinsulinism","termid":"MONDO:0015624"},{"relation_name":"is_a","term_name":"disorder of carbohydrate transmembrane transport and absorption","termid":"MONDO:0017706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0004335","MONDO:0005066"],"is_obsolete":false,"name":"exercise-induced hyperinsulinism","secondary_identifiers":["GARD:9932","OMIM:610021","NCIT:C131839","UMLS:C1864902","DOID:0070214","icd11.foundation:999935139","MEDGEN:351246","SCTID:715830008","MESH:C538376"],"synonyms":[{"name":"EIHI","type":"exact"},{"name":"HHF7","type":"related"},{"name":"MCT1 hyperinsulinism","type":"exact"},{"name":"exercise induced hyperinsulinemic hypoglycemia","type":"related"},{"name":"exercise-induced hyperinsulinemic hypoglycemia","type":"exact"},{"name":"hyperinsulinemic hypoglycemia exercise-induced","type":"related"},{"name":"hyperinsulinemic hypoglycemia familial 7","type":"related"},{"name":"hyperinsulinemic hypoglycemia, exercise-induced","type":"related"},{"name":"hyperinsulinemic hypoglycemia, familial, 7","type":"related"},{"name":"hyperinsulinemic hypoglycemia, familial, type 7","type":"exact"},{"name":"hyperinsulinism due to SLC16A1 deficiency","type":"exact"},{"name":"hyperinsulinism due to monocarboxylate transporter 1 deficiency","type":"exact"},{"name":"monocarboxylate transporter 1 hyperinsulinism","type":"exact"}],"termid":"MONDO:0012396","xrefs":{"Monarch":{"xref_id":"0012396"}}}


id: MONDO:1012785
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cerebellar ataxia that occurs in dogs due to a mutation in the ITPR1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar ataxia, dog","termid":"MONDO:1012957"},{"relation_name":"is_a","term_name":"hereditary cerebellar ataxia, non-human animal","termid":"MONDO:1012960"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinocerebellar ataxia, ITPR1-related, dog","secondary_identifiers":["OMIA:002097-9615"],"synonyms":[{"name":"SCAIS","type":"exact"},{"name":"ataxia, spinocerebellar, ITPR1-related, dog","type":"exact"}],"termid":"MONDO:1012785","xrefs":{"Monarch":{"xref_id":"1012785"}}}


id: GO:0010994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of creating free ubiquitin chains, compounds composed of a large number of ubiquitin monomers. These chains are not conjugated to a protein.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein polymerization","termid":"GO:0051258"},{"relation_name":"part_of","term_name":"ubiquitin recycling","termid":"GO:0010992"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0065003"],"is_obsolete":false,"name":"free ubiquitin chain polymerization","termid":"GO:0010994"}


id: PBO:0083415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the essential ORF SEC61/YLR378C","termid":"PBO:0083415"}


id: MONDO:0001813
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"blepharitis","termid":"MONDO:0004785"}],"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":"squamous blepharitis","secondary_identifiers":["ICD9:373.02","DOID:13825","UMLS:C0155174","MEDGEN:509829","SCTID:58912008"],"termid":"MONDO:0001813","xrefs":{"Monarch":{"xref_id":"0001813"}}}


id: PBO:0070763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10 pseudogene 19","termid":"PBO:0070763"}


id: MONDO:0018212
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of cervical artery dissection that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"cervical artery dissection","termid":"MONDO:0006061"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial cervical artery dissection","secondary_identifiers":["Orphanet:36382","GARD:18823","UMLS:C4755308","MEDGEN:1659372"],"synonyms":[{"name":"familial CAD","type":"exact"},{"name":"hereditary CAD","type":"exact"},{"name":"hereditary cervical artery dissection","type":"exact"}],"termid":"MONDO:0018212","xrefs":{"Monarch":{"xref_id":"0018212"}}}


id: PBO:0058226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4516","termid":"PBO:0058226"}


id: GO:2001155
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glucose catabolic process to ethanol.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"negative regulation of fermentation","termid":"GO:1901003"},{"relation_name":"is_a","term_name":"regulation of glycolytic fermentation to ethanol","termid":"GO:2001154"},{"relation_name":"negatively_regulates","term_name":"glycolytic fermentation to ethanol","termid":"GO:0019655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"negatively_regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281","GO:0006091"],"is_obsolete":false,"name":"negative regulation of glycolytic fermentation to ethanol","synonyms":[{"name":"negative regulation of ethanol fermentation","type":"exact"},{"name":"negative regulation of glucose fermentation to ethanol","type":"exact"}],"termid":"GO:2001155"}


id: GO:0035217
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Progression of the labial imaginal disc over time, from its initial formation through to its metamorphosis to form adult structures including parts of the proboscis.","definition_xrefs":["GOC:bf","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc development","termid":"GO:0007444"}],"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":"labial disc development","termid":"GO:0035217"}


id: PBO:0073936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 17 member 8","termid":"PBO:0073936"}


id: MONDO:0043240
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of arthritis that affects hemophiliacs, which is characterized by bleeding into the joint space.","definition_xrefs":["NCIT:C27039"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthritic joint disease","termid":"MONDO:0005578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemophilic arthropathy","secondary_identifiers":["SCTID:80813006","UMLS:C0263725","MEDGEN:120487"],"synonyms":[{"name":"arthropathy in haemophilia","type":"related"},{"name":"arthropathy in hemophilia","type":"related"},{"name":"hemophilic arthritis","type":"exact"},{"name":"hemophilic arthropathy","type":"exact"}],"termid":"MONDO:0043240","xrefs":{"Monarch":{"xref_id":"0043240"}}}


id: MONDO:0971007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neuroocular syndrome","termid":"MONDO:0859193"}],"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":"neuroocular syndrome 1","secondary_identifiers":["Orphanet:659904","OMIM:619539","UMLS:C5925133","MEDGEN:1863661"],"termid":"MONDO:0971007","xrefs":{"Monarch":{"xref_id":"0971007"}}}


id: FYPO:0001005
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which DNA is broken into small fragments when the cell is subject to nitrogen starvation.","definition_xrefs":["PMID:19366728","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fragmented DNA","termid":"FYPO:0000160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"fragmented DNA during nitrogen starvation","synonyms":[{"name":"DNA fragmentation during nitrogen starvation","type":"exact"},{"name":"fragmented DNA during nitrogen depletion","type":"exact"},{"name":"fragmented DNA during nitrogen deprivation","type":"exact"},{"name":"fragmented nucleus during nitrogen starvation","type":"related"}],"termid":"FYPO:0001005"}


id: MONDO:0006548
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Facial Dermatosis, also known as facial dermatoses, is related tolipogranulomatosis. An important gene associated with Facial Dermatosis isCCNE1(cyclin E1). The drugsbetamethasoneandbetamethasone acetatehave been mentioned in the context of this disorder.","definition_xrefs":["EFO:1000698"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"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":"facial dermatosis","secondary_identifiers":["DOID:3134","UMLS:C0015456","MEDGEN:8760","MESH:D005148"],"termid":"MONDO:0006548","xrefs":{"Monarch":{"xref_id":"0006548"}}}


id: PBO:0059166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MPV17 mitochondrial inner membrane protein like","termid":"PBO:0059166"}


id: FYPO:0007472
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which histone exchange is abnormal. Histone exchange is replacement, within chromatin, of resident histones or histone subunits with alternative, sometimes variant, histones or subunits.","definition_xrefs":["PomBase:mah","GO:0043486","PMID:31315658"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal dynamic protein localization pattern","termid":"FYPO:0006606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abnormal histone turnover","termid":"FYPO:0007472"}


id: PBO:0087148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-Dependent ATPase, member of DExD/H-box family; involved in cleavage of site A3 within the ITS1 spacer during rRNA processing; not essential for growth, but deletion causes severe slow-growth phenotype","termid":"PBO:0087148"}


id: GO:0018767
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-hydroxy-6-oxo-7-methylocta-2,4-dienoate + H2O = cis-2-hydroxypenta-2,4-dienoate + isobutyrate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-hydroxy-6-oxo-7-methylocta-2,4-dienoate hydrolase activity (obsolete GO:0018767)","termid":"GO:0018767"}


id: PBO:0073686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signaling threshold regulating transmembrane adaptor 1","termid":"PBO:0073686"}


id: PBO:0079395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TUBB4B pseudogene 2","termid":"PBO:0079395"}


id: MONDO:0859357
data:
  {"annotated_genes":["SJAG_01940"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85329],"is_not":false,"summary":null,"term":"MONDO:0859357"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01940":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"congenital disorder of glycosylation, type IIz","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620201","UMLS:C5774295","MEDGEN:1824068"],"termid":"MONDO:0859357","terms_by_termid":{"MONDO:0859357":null},"xrefs":{"Monarch":{"xref_id":"0859357"}}}


id: FYPO:0000232
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cytokinesis phenotype observed in the vegetative growth phase of the life cycle in which the actomyosin contractile ring splits upon initiation of contraction during anaphase B, resulting in the formation of a primary ring that undergoes constriction and a secondary ring that does not constrict.","definition_xrefs":["PMID:18272786","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring morphology","termid":"FYPO:0003338"}],"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":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000631","FYPO:0004803","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"split actomyosin contractile ring","synonyms":[{"name":"abnormal contractile ring contraction with contractile ring splitting","type":"related"},{"name":"actomyosin contractile ring splitting","type":"related"},{"name":"actomyosin contractile ring splitting upon contraction","type":"related"},{"name":"cytokinesis defects, splitting of the actinomyosin ring","type":"related"},{"name":"split actomyosin contractile ring during mitotic cell cycle","type":"related"},{"name":"split actomyosin contractile ring during vegetative growth","type":"exact"},{"name":"split cytokinetic contractile ring","type":"exact"},{"name":"split mitotic contractile ring","type":"exact"}],"termid":"FYPO:0000232"}


id: PBO:0026786
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ascus_morphology","termid":"PBO:0026786"}


id: PBO:0001832
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.2.1.75","termid":"PBO:0001832"}


id: MONDO:0006008
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic inflammation of the vestibular nerve, characterized clinically by the acute or subacute onset of vertigo; nausea; and imbalance. The cochlear nerve is typically spared and hearing loss and tinnitus do not usually occur. Symptoms usually resolve over a period of days to weeks. (Adams et al., Principles of Neurology, 6th ed, p304)","definition_xrefs":["MESH:D020338"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibulocochlear nerve disorder","termid":"MONDO:0001563"},{"relation_name":"is_a","term_name":"neuritis","termid":"MONDO:0002122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"vestibular neuronitis","secondary_identifiers":["SCTID:186738001","MEDGEN:155655","ICD10CM:H81.2","UMLS:C0751908","DOID:12683","EFO:0007537","ICD9:078.81","ICD9:386.12"],"synonyms":[{"name":"epidemic neurolabyrinthitis","type":"exact"},{"name":"vestibular neuritis","type":"exact"}],"termid":"MONDO:0006008","xrefs":{"Monarch":{"xref_id":"0006008"}}}


id: MONDO:0012466
data:
  {"annotated_genes":["SJAG_03258","SJAG_00737"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87043,87044],"is_not":false,"summary":null,"term":"MONDO:0012466"}]},"cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing young-onset Parkinson disease, in which the cause of the disease is a mutation in the HTRA2 gene.","definition_xrefs":["MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00737":null,"SJAG_03258":null},"genotype_count":0,"is_obsolete":false,"name":"Parkinson disease 13, autosomal dominant, susceptibility to","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C565204","UMLS:C1853202","MEDGEN:343992","OMIM:610297"],"synonyms":[{"name":"HTRA2 young-onset Parkinson disease","type":"exact"},{"name":"PARK13","type":"exact"},{"name":"Parkinson disease 13","type":"exact"},{"name":"Parkinson disease 13, autosomal dominant, susceptibility to","type":"exact"},{"name":"young-onset Parkinson disease caused by mutation in HTRA2","type":"exact"}],"termid":"MONDO:0012466","terms_by_termid":{"MONDO:0012466":null},"xrefs":{"Monarch":{"xref_id":"0012466"}}}


id: MONDO:0012642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bipolar disorder","termid":"MONDO:0004985"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major affective disorder 4","secondary_identifiers":["MEDGEN:372671","MESH:C567073","OMIM:611247","UMLS:C1970943"],"synonyms":[{"name":"MAFD4","type":"exact"},{"name":"MAJOR affective disorder 4","type":"related"},{"name":"bipolar affective disorder","type":"related"},{"name":"major affective disorder 4","type":"exact"}],"termid":"MONDO:0012642","xrefs":{"Monarch":{"xref_id":"0012642"}}}


id: PBO:0084520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of Hsp110 subclass of the heat shock protein 70 (HSP70) family; serves as nucleotide exchange factor to load ATP onto the SSA class of cytosolic Hsp70s; may be involved in protein folding; localized to the cytoplasm; SSE2 has a paralog, SSE1, that arose from the whole genome duplication","termid":"PBO:0084520"}


id: PBO:0088673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, nutritional copper sensing Cuf1","termid":"PBO:0088673"}


id: GO:1990453
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex involved in the disassembly and subsequent reassembly of nucleosomes. It associates with the coding region of transcriptionally active genes where it interacts with the RNA polymerase II and affects its processivity during co-transcriptional RNA processing and maturation. It exists as a functionally independent part of the NuA4 complex.","definition_xrefs":["GOC:bhm","PMID:24843044"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"nucleosome disassembly/reassembly complex","synonyms":[{"name":"eaf5/7/3 complex","type":"narrow"}],"termid":"GO:1990453"}


id: MONDO:0023646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lipodermatosclerosis refers to changes in the skin of the lower legs. It is a form of panniculitis (inflammation of the layer of fat under the skin). Signs and symptoms include pain, hardening of skin, change in skin color (redness), swelling, and a tapering of the legs above the ankles. The exact underlying cause is unknown; however, it appears to be associated with venous insufficiency and/or obesity. Treatment usually includes compression therapy.","definition_xrefs":["GARD:0009671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatitis","termid":"MONDO:0002406"},{"relation_name":"is_a","term_name":"panniculitis","termid":"MONDO:0006591"},{"relation_name":"is_a","term_name":"localized scleroderma","termid":"MONDO:0019562"}],"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:0005093","MONDO:0005046"],"is_obsolete":false,"name":"lipodermatosclerosis","secondary_identifiers":["SCTID:410016009","UMLS:C0406500","icd11.foundation:473315619","GARD:9671","MESH:C537026","MEDGEN:140802"],"synonyms":[{"name":"acute lipodermatosclerosis","type":"related"},{"name":"hypodermitis sclerodermaformis","type":"related"},{"name":"sclerosing panniculitis","type":"related"}],"termid":"MONDO:0023646","xrefs":{"Monarch":{"xref_id":"0023646"}}}


id: MONDO:0012729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial polycythemia in which the cause of the disease is a mutation in the EPAS1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial polycythemia","termid":"MONDO:0001115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"erythrocytosis, familial, 4","secondary_identifiers":["MESH:C567086","OMIM:611783","UMLS:C2673187","GARD:18356","MEDGEN:435867","DOID:0080339"],"synonyms":[{"name":"ECYT4","type":"related"},{"name":"EPAS1 familial polycythemia","type":"exact"},{"name":"erythrocytosis, familial, 4","type":"exact"},{"name":"erythrocytosis, familial, type 4","type":"exact"},{"name":"familial polycythemia caused by mutation in EPAS1","type":"exact"}],"termid":"MONDO:0012729","xrefs":{"Monarch":{"xref_id":"0012729"}}}


id: PBO:0050160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 16","termid":"PBO:0050160"}


id: MONDO:0017014
data:
  {"annotated_genes":["SJAG_02805","SJAG_00570"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010926"},{"annotations":[85974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011871"}]},"cv_name":"mondo","definition":"A interstitial lung disease that occurs during childhood.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interstitial lung disease","termid":"MONDO:0015925"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00570":null,"SJAG_02805":null},"genotype_count":0,"is_obsolete":false,"name":"interstitial lung disease specific to childhood","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:328661000119108","MEDGEN:1842412","Orphanet:264656","UMLS:C5679752"],"synonyms":[{"name":"ILD specific to childhood","type":"exact"},{"name":"chILD","type":"exact"},{"name":"chILD syndrome","type":"exact"},{"name":"childhood interstitial lung disease","type":"exact"},{"name":"interstitial lung disease of childhood","type":"exact"},{"name":"paediatric interstitial lung disease","type":"exact"},{"name":"pediatric interstitial lung disease","type":"exact"}],"termid":"MONDO:0017014","terms_by_termid":{"MONDO:0010926":null,"MONDO:0011871":null},"xrefs":{"Monarch":{"xref_id":"0017014"}}}


id: PBO:0075051
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 116-14","termid":"PBO:0075051"}


id: PR:Q9Y7Y7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gas4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7Y7"],"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":"1,3-beta-glucanosyltransferase gas4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC342.03","synonyms":[{"name":"Spom972h-gas4","type":"exact"}],"termid":"PR:Q9Y7Y7"}


id: GO:0090677
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A phenotypic switching process where a cell reversibly differentiates and dedifferentiates from one cell type into another.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenotypic switching","termid":"GO:0036166"}],"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":"reversible differentiation","termid":"GO:0090677"}


id: PBO:0061895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opsin 1, medium wave sensitive 3","termid":"PBO:0061895"}


id: PBO:0005049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexose transporter Ght5","termid":"PBO:0005049"}


id: GO:0035573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The trimethylation of the N-terminal serine of proteins to form the derivative N,N,N-trimethylserine.","definition_xrefs":["PMID:20668449"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-terminal peptidyl-serine methylation","termid":"GO:0035570"}],"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":"N-terminal peptidyl-serine trimethylation","termid":"GO:0035573"}


id: GO:1902817
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein localization to microtubule.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:vw","PMID:23087209"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to microtubule","termid":"GO:1902816"},{"relation_name":"is_a","term_name":"negative regulation of protein localization","termid":"GO:1903828"},{"relation_name":"negatively_regulates","term_name":"protein localization to microtubule","termid":"GO:0035372"}],"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 protein localization to microtubule","synonyms":[{"name":"down regulation of protein localisation to microtubule","type":"exact"},{"name":"down regulation of protein localization to microtubule","type":"exact"},{"name":"down-regulation of protein localisation to microtubule","type":"exact"},{"name":"down-regulation of protein localization to microtubule","type":"exact"},{"name":"downregulation of protein localisation to microtubule","type":"exact"},{"name":"downregulation of protein localization to microtubule","type":"exact"},{"name":"inhibition of protein localisation to microtubule","type":"narrow"},{"name":"inhibition of protein localization to microtubule","type":"narrow"},{"name":"negative regulation of protein localisation to microtubule","type":"exact"}],"termid":"GO:1902817"}


id: PR:Q9P7M3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- slx1 gene.","definition_xrefs":["UniProtKB:Q9P7M3","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":"structure-specific endonuclease subunit slx1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.15","synonyms":[{"name":"Spom972h-slx1","type":"exact"}],"termid":"PR:Q9P7M3"}


id: MONDO:0003857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A solitary fibrous tumor/hemangiopericytoma, grade 3 that arises from the brain and occurs in the adult population.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete connective tissue cancer (obsolete MONDO:0002176)","termid":"MONDO:0002176"},{"relation_name":"is_a","term_name":"hemangiopericytoma","termid":"MONDO:0005094"},{"relation_name":"is_a","term_name":"malignant central nervous system mesenchymal, non-meningothelial neoplasm","termid":"MONDO:0037740"}],"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":"adult intracranial malignant hemangiopericytoma","secondary_identifiers":["DOID:6333","MEDGEN:235288","NCIT:C9183","UMLS:C1334558"],"synonyms":[{"name":"adult intracranial anaplastic hemangiopericytoma","type":"exact"},{"name":"adult intracranial solitary fibrous tumor/hemangiopericytoma, grade 3","type":"exact"},{"name":"adult malignant intracranial hemangiopericytoma","type":"exact"},{"name":"central nervous system solitary fibrous tumor/hemangiopericytoma, grade 3","type":"exact"},{"name":"malignant adult intracranial hemangiopericytoma","type":"exact"}],"termid":"MONDO:0003857","xrefs":{"Monarch":{"xref_id":"0003857"}}}


id: PBO:0057528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 645","termid":"PBO:0057528"}


id: PBO:0075493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA31 subfamily F member 3","termid":"PBO:0075493"}


id: PBO:0052667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 35","termid":"PBO:0052667"}


id: MONDO:0012619
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 11","secondary_identifiers":["UMLS:C1970193","MEDGEN:369677","GARD:22546","DOID:0081186","MESH:C567012","OMIM:611097"],"synonyms":[{"name":"MRT11","type":"exact"},{"name":"intellectual disability, autosomal recessive 11","type":"exact"},{"name":"mental retardation, autosomal recessive 11","type":"related"},{"name":"mental retardation, autosomal recessive, 11","type":"exact"}],"termid":"MONDO:0012619","xrefs":{"Monarch":{"xref_id":"0012619"}}}


id: PBO:0071594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 11","termid":"PBO:0071594"}


id: PBO:0058749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6873","termid":"PBO:0058749"}


id: PBO:0057697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1285-2","termid":"PBO:0057697"}


id: MOD:02045
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an L-glutamic acid residue crosslinked to one or more amino acid residues.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crosslinked L-glutamic acid residue","synonyms":[{"name":"XlnkGlu","type":"exact"}],"termid":"MOD:02045"}


id: PBO:0070517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L6 pseudogene 16","termid":"PBO:0070517"}


id: PBO:0110340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement C4A (Chido/Rodgers blood group)","termid":"PBO:0110340"}


id: PR:P06652
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An M-phase inducer phosphatase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PMID:9774107","PomBase:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"M-phase inducer phosphatase","termid":"PR:000027506"},{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-phase inducer phosphatase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24H6.05","secondary_identifiers":["UniProtKB:P06652","PR:000027507"],"synonyms":[{"name":"SPAC24H6.05","type":"related"},{"name":"Spom972h-cdc25","type":"exact"}],"termid":"PR:P06652"}


id: PBO:0060456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear apoptosis inducing factor 1","termid":"PBO:0060456"}


id: MONDO:0014450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any isolated congenital breast hypoplasia/aplasia in which the cause of the disease is a mutation in the PTPRF gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated congenital breast hypoplasia/aplasia","termid":"MONDO:0015855"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breasts and/or nipples, aplasia or hypoplasia of, 2","secondary_identifiers":["UMLS:C4014918","OMIM:616001","GARD:16044","MEDGEN:863355"],"synonyms":[{"name":"BNAH2","type":"related"},{"name":"PTPRF isolated congenital breast hypoplasia/aplasia","type":"exact"},{"name":"breasts and/or nipples, aplasia or hypoplasia of, 2","type":"exact"},{"name":"breasts and/or nipples, aplasia or hypoplasia of, type 2","type":"exact"},{"name":"isolated congenital breast hypoplasia/aplasia caused by mutation in PTPRF","type":"exact"}],"termid":"MONDO:0014450","xrefs":{"Monarch":{"xref_id":"0014450"}}}


id: PBO:0044350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 35","termid":"PBO:0044350"}


id: MONDO:0009035
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive form of craniometaphyseal dysplasia.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"craniometaphyseal dysplasia","termid":"MONDO:0015465"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"craniometaphyseal dysplasia, autosomal recessive","secondary_identifiers":["UMLS:C2931244","MESH:C536570","DOID:0080802","MEDGEN:419753","GARD:1582","OMIM:218400"],"synonyms":[{"name":"CMDR","type":"related"},{"name":"autosomal recessive craniometaphyseal dysplasia","type":"exact"},{"name":"craniometaphyseal dysplasia, autosomal recessive","type":"exact"},{"name":"craniometaphyseal dysplasia, autosomal recessive type","type":"related"}],"termid":"MONDO:0009035","xrefs":{"Monarch":{"xref_id":"0009035"}}}


id: PBO:0053227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing G protein-coupled receptor 4","termid":"PBO:0053227"}


id: PBO:0076979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine hydroxylase","termid":"PBO:0076979"}


id: MONDO:0013255
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any arthrogryposis-renal dysfunction-cholestasis syndrome in which the cause of the disease is a mutation in the VIPAS39 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis-renal dysfunction-cholestasis syndrome","termid":"MONDO:0017123"}],"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":"arthrogryposis, renal dysfunction, and cholestasis 2","secondary_identifiers":["UMLS:C3150672","OMIM:613404","MEDGEN:462022","DOID:0111354","GARD:15658"],"synonyms":[{"name":"ARCS2","type":"related"},{"name":"VIPAS39 arthrogryposis-renal dysfunction-cholestasis syndrome","type":"exact"},{"name":"arthrogryposis, renal dysfunction, and cholestasis 2","type":"exact"},{"name":"arthrogryposis, renal dysfunction, and cholestasis type 2","type":"exact"},{"name":"arthrogryposis-renal dysfunction-cholestasis syndrome caused by mutation in VIPAS39","type":"exact"}],"termid":"MONDO:0013255","xrefs":{"Monarch":{"xref_id":"0013255"}}}


id: PBO:0070757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10 pseudogene 13","termid":"PBO:0070757"}


id: FYPO:0003185
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the microtubule cytoskeleton is normal (i.e. indistinguishable from wild type) during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to cytoskeleton during vegetative growth","termid":"FYPO:0003184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal protein localization to microtubule cytoskeleton during mitotic interphase","synonyms":[{"name":"normal protein localisation to microtubule cytoskeleton during mitotic interphase","type":"exact"},{"name":"normal protein localization to microtubule cytoskeleton during interphase during vegetative growth","type":"exact"}],"termid":"FYPO:0003185"}


id: PBO:0042732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere protein J","termid":"PBO:0042732"}


id: PBO:0073668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal induced proliferation associated 1 like 3","termid":"PBO:0073668"}


id: MONDO:0005008
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The most common type of colorectal carcinoma. It is characterized by the presence of malignant glandular epithelial cells invading through the muscularis mucosa into the submucosa. Histologic variants include mucinous adenocarcinoma, signet ring cell carcinoma, medullary carcinoma, serrated adenocarcinoma, cribriform comedo-type adenocarcinoma, and micropapillary adenocarcinoma.","definition_xrefs":["NCIT:C5105"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"colorectal carcinoma","termid":"MONDO:0024331"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"colorectal adenocarcinoma","secondary_identifiers":["DOID:0050913","UMLS:C1319315","SCTID:408645001","ONCOTREE:COADREAD","MEDGEN:230816","SCTID:269533000","DOID:0050861","EFO:0000365"],"synonyms":[{"name":"adenocarcinoma of large bowel","type":"exact"},{"name":"adenocarcinoma of large intestine","type":"exact"},{"name":"adenocarcinoma of the large bowel","type":"exact"},{"name":"adenocarcinoma of the large intestine","type":"exact"},{"name":"colorectal (colon or rectal) adenocarcinoma","type":"exact"},{"name":"colorectal adenocarcinoma","type":"exact"},{"name":"colorectum adenocarcinoma","type":"exact"},{"name":"large bowel adenocarcinoma","type":"exact"},{"name":"large intestine adenocarcinoma","type":"exact"}],"termid":"MONDO:0005008","xrefs":{"Monarch":{"xref_id":"0005008"}}}


id: PBO:0058222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4512","termid":"PBO:0058222"}


id: PBO:0075422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm associated antigen 8","termid":"PBO:0075422"}


id: PBO:0051585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 18 receptor 1","termid":"PBO:0051585"}


id: GO:0033285
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + monocarboxylic acid(out/in) = ADP + phosphate + monocarboxylic acid(in/out).","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transmembrane transporter activity","termid":"GO:0008028"},{"relation_name":"is_a","term_name":"ATPase-coupled carboxylic acid transmembrane transporter activity","termid":"GO:0033284"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"ATPase-coupled monocarboxylic acid transmembrane transporter activity","synonyms":[{"name":"ATP-dependent monocarboxylic acid transmembrane transporter activity","type":"exact"},{"name":"monocarboxylic acid-transporting ATPase activity","type":"exact"}],"termid":"GO:0033285"}


id: FYPO:0003002
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 centromere of a chromosome is decreased during metaphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to centromere during vegetative growth","termid":"FYPO:0000450"},{"relation_name":"is_a","term_name":"abnormal protein localization to centromere during mitotic metaphase","termid":"FYPO:0006175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein localization to centromere during mitotic metaphase","synonyms":[{"name":"decreased protein localisation to centromere during mitotic metaphase","type":"exact"},{"name":"decreased protein localisation to chromosome, centromeric region during mitotic metaphase","type":"exact"},{"name":"decreased protein localization to centromere during metaphase during vegetative growth","type":"exact"},{"name":"decreased protein localization to chromosome, centric region during mitotic metaphase","type":"exact"},{"name":"decreased protein localization to chromosome, centromeric region during mitotic metaphase","type":"exact"},{"name":"reduced protein localization to centromere during mitotic metaphase","type":"exact"}],"termid":"FYPO:0003002"}


id: PBO:0086497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative pimeloyl-CoA synthetase involved in biotin biosynthesis; in S. cerevisiae strains YJM627 and A364a; highly degraded pseudogenic copy of BIO1/YAR070W-A, which is a paralog of YJR154W","termid":"PBO:0086497"}


id: GO:0035251
data:
  {"annotated_genes":["SJAG_01531","SJAG_03587","SJAG_04571","SJAG_00876","SJAG_05285","SJAG_02222","SJAG_01288","SJAG_00394","SJAG_00129","SJAG_01427"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112909,75635,74562,79853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003843"},{"annotations":[100816,93116,78762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003825"},{"annotations":[115565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140752"},{"annotations":[66660],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004581"},{"annotations":[79303],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003980"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a glucosyl group from UDP-glucose to an acceptor molecule.","definition_xrefs":["PMID:19858195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glycosyltransferase activity","termid":"GO:0008194"},{"relation_name":"is_a","term_name":"glucosyltransferase activity","termid":"GO:0046527"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00129":null,"SJAG_00394":null,"SJAG_00876":null,"SJAG_01288":null,"SJAG_01427":null,"SJAG_01531":null,"SJAG_02222":null,"SJAG_03587":null,"SJAG_04571":null,"SJAG_05285":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:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"UDP-glucosyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-1912353"],"termid":"GO:0035251","terms_by_termid":{"GO:0003825":null,"GO:0003843":null,"GO:0003980":null,"GO:0004581":null,"GO:0140752":null}}


id: PBO:0027647
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_BE49385A","termid":"PBO:0027647"}


id: PBO:0043018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHL1 antisense RNA 2","termid":"PBO:0043018"}


id: PBO:0077780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tonsoku like, DNA repair protein","termid":"PBO:0077780"}


id: PBO:0045336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DOCK9 divergent transcript","termid":"PBO:0045336"}


id: MONDO:0020617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete blood group--ok (obsolete MONDO:0020617)","secondary_identifiers":["OMIM:111380"],"synonyms":[{"name":"BLOOD GROUP--OK","type":"related"},{"name":"OK","type":"related"},{"name":"blood group, OK","type":"exact"}],"termid":"MONDO:0020617","xrefs":{"Monarch":{"xref_id":"0020617"}}}


id: PBO:0073120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine dehydratase like","termid":"PBO:0073120"}


id: PR:Q09905
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is encoded by the Schizosaccharomyces pombe 972h- aps3 gene.","definition_xrefs":["PRO:DAN"],"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":"AP-3 complex subunit sigma (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC30D11.05","secondary_identifiers":["UniProtKB:Q09905"],"synonyms":[{"name":"AP-3 complex sigma3A subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-aps3","type":"exact"},{"name":"adaptor-related protein complex 3 subunit sigma (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"clathrin-associated/assembly/adaptor protein, small 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"sigma-adaptin 3A (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"sigma3-adaptin (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09905"}


id: PBO:0080836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y-box binding protein 1","termid":"PBO:0080836"}


id: PBO:0044807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 105B","termid":"PBO:0044807"}


id: PBO:0000504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy associated protein Aut12 (predicted)","termid":"PBO:0000504"}


id: GO:0033084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of immature T cell proliferation in the thymus.","definition_xrefs":["GOC:add","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of immature T cell proliferation","termid":"GO:0033083"},{"relation_name":"regulates","term_name":"immature T cell proliferation in thymus","termid":"GO:0033080"}],"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 immature T cell proliferation in thymus","synonyms":[{"name":"regulation of thymic T cell proliferation","type":"exact"},{"name":"regulation of thymocyte cell proliferation","type":"exact"},{"name":"regulation of thymocyte proliferation","type":"exact"}],"termid":"GO:0033084"}


id: MONDO:0014153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cone-rod dystrophy in which the cause of the disease is a mutation in the RAB28 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy","termid":"MONDO:0015993"},{"relation_name":"is_a","term_name":"RAB28-related retinopathy","termid":"MONDO:0100448"}],"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":"cone-rod dystrophy 18","secondary_identifiers":["DOID:0111024","OMIM:615374","UMLS:C3809299","GARD:15953","MEDGEN:815629"],"synonyms":[{"name":"CORD18","type":"exact"},{"name":"RAB28 cone-rod dystrophy","type":"exact"},{"name":"cone-rod dystrophy 18","type":"exact"},{"name":"cone-rod dystrophy caused by mutation in RAB28","type":"exact"},{"name":"cone-rod dystrophy type 18","type":"exact"}],"termid":"MONDO:0014153","xrefs":{"Monarch":{"xref_id":"0014153"}}}


id: PBO:0068616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 68, pseudogene","termid":"PBO:0068616"}


id: GO:1904031
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cyclin-dependent protein kinase activity.","definition_xrefs":["PMID:22995177","GO_REF:0000059","GOC:als","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein kinase activity","termid":"GO:0045860"}],"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 cyclin-dependent protein kinase activity","synonyms":[{"name":"activation of cyclin-dependent protein kinase activity","type":"narrow"},{"name":"up regulation of cyclin-dependent protein kinase activity","type":"exact"},{"name":"up-regulation of cyclin-dependent protein kinase activity","type":"exact"},{"name":"upregulation of cyclin-dependent protein kinase activity","type":"exact"}],"termid":"GO:1904031"}


id: MONDO:0013771
data:
  {"annotated_genes":["SJAG_01012","SJAG_00409"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86429,86430],"is_not":false,"summary":null,"term":"MONDO:0013771"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"liver disorder","termid":"MONDO:0005154"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00409":null,"SJAG_01012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"transient infantile hypertriglyceridemia and hepatosteatosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:17363","Orphanet:300293","MEDGEN:482583","UMLS:C3280953","OMIM:614480"],"synonyms":[{"name":"HTGTI","type":"related"},{"name":"hypertriglyceridemia, transient infantile","type":"related"},{"name":"transient infantile hypertriglyceridemia and fatty liver","type":"exact"},{"name":"transient infantile hypertriglyceridemia and hepatosteatosis","type":"exact"}],"termid":"MONDO:0013771","terms_by_termid":{"MONDO:0013771":null},"xrefs":{"Monarch":{"xref_id":"0013771"}}}


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


id: PBO:0003031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enhancer of RNA-mediated gene silencing","termid":"PBO:0003031"}


id: PBO:0086828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; YOR338W transcription is regulated by Azf1p and its transcript is a specific target of the G protein effector Scp160p; identified as being required for sporulation in a high-throughput mutant screen; YOR338W has a paralog, FUN19, that arose from the whole genome duplication","termid":"PBO:0086828"}


id: PBO:0044810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 107A","termid":"PBO:0044810"}


id: PBO:0069722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1003, pseudogene","termid":"PBO:0069722"}


id: PBO:0030326
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_wall_biogenesis","termid":"PBO:0030326"}


id: PR:O13746
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC16E8.18 gene.","definition_xrefs":["UniProtKB:O13746","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C16E8.18 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16E8.18","synonyms":[{"name":"Spom972h-SPAC16E8.18","type":"exact"}],"termid":"PR:O13746"}


id: GO:0072764
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a reversine stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to purine-containing compound","termid":"GO:0071415"},{"relation_name":"is_a","term_name":"response to reversine","termid":"GO:1901596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to reversine","termid":"GO:0072764"}


id: MONDO:0012633
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete malaria (obsolete MONDO:0012633)","termid":"MONDO:0012633","xrefs":{"Monarch":{"xref_id":"0012633"}}}


id: GO:1901557
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 fenofibrate stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to ether","termid":"GO:0045472"},{"relation_name":"is_a","term_name":"response to ketone","termid":"GO:1901654"}],"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 fenofibrate","termid":"GO:1901557"}


id: MONDO:0020224
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare cataract.","gene_count":0,"genotype_count":0,"name":"obsolete rare cataract (obsolete MONDO:0020224)","secondary_identifiers":["Orphanet:98640"],"synonyms":[{"name":"rare cataract","type":"exact"},{"name":"rare cataract (disease)","type":"exact"}],"termid":"MONDO:0020224","xrefs":{"Monarch":{"xref_id":"0020224"}}}


id: MONDO:0005724
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute or chronic, localized or disseminated infection by Cryptococcus neoformans. Sites of involvement include the lungs, central nervous system and meninges, skin, and visceral organs.--2004","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opportunistic mycosis","termid":"MONDO:0002312"},{"relation_name":"is_a","term_name":"parasitic infectious disease","termid":"MONDO:0005135"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cryptococcosis","secondary_identifiers":["MEDGEN:8189","UMLS:C0010414","GARD:6218","EFO:0007229","ICD10CM:B45","icd11.foundation:390527954","DOID:12053","ICD9:117.5","MedDRA:10011490","NCIT:C2967","NORD:1019","MESH:D003453","Orphanet:1546","SCTID:42386007"],"synonyms":[{"name":"Busse-Buschke's disease","type":"exact"},{"name":"Cryptococcal infection","type":"exact"},{"name":"Cryptococcus neoformans caused disease or disorder","type":"exact"},{"name":"Cryptococcus neoformans disease or disorder","type":"exact"},{"name":"Cryptococcus neoformans infectious disease","type":"exact"},{"name":"European cryptococcosis","type":"exact"},{"name":"cryptococcus neoformans infection","type":"related"},{"name":"torula","type":"exact"},{"name":"torulosis","type":"exact"}],"termid":"MONDO:0005724","xrefs":{"Monarch":{"xref_id":"0005724"}}}


id: MONDO:0012673
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"colorectal cancer","termid":"MONDO:0005575"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colorectal cancer, susceptibility to, 2","secondary_identifiers":["OMIM:611469","MEDGEN:369417","UMLS:C1969113"],"synonyms":[{"name":"CRCS2","type":"exact"},{"name":"colorectal cancer, susceptibility to, 2","type":"exact"},{"name":"colorectal cancer, susceptibility to, on chromosome 8Q24","type":"related"}],"termid":"MONDO:0012673","xrefs":{"Monarch":{"xref_id":"0012673"}}}


id: FYPO:0008137
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 lipid droplets are smaller and more numerous than normal.","definition_xrefs":["PMID:35658118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal lipid droplet organization","termid":"FYPO:0000808"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased size and number of lipid droplets","termid":"FYPO:0008137"}


id: GO:0075330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of symbiont arbuscule formation for nutrient acquisition from host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of formation of structure involved in a symbiotic process","termid":"GO:0044149"},{"relation_name":"is_a","term_name":"regulation of arbuscule formation for nutrient acquisition from host","termid":"GO:0075329"},{"relation_name":"positively_regulates","term_name":"formation of arbuscule for nutrient acquisition","termid":"GO:0075328"}],"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 arbuscule formation for nutrient acquisition from host","termid":"GO:0075330"}


id: PBO:0049391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP binding protein 4","termid":"PBO:0049391"}


id: FYPO:0007027
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 medial cortex is abolished, and the protein is present in the cytoplasm instead.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to medial cortex during vegetative growth","termid":"FYPO:0002555"},{"relation_name":"is_a","term_name":"abolished protein localization to cell cortex, with protein mislocalized to cytoplasm, during vegetative growth","termid":"FYPO:0005501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to medial cortex, with protein mislocalized to cytoplasm, during vegetative growth","synonyms":[{"name":"abolished protein localisation to medial cortex, with protein mislocalised to cytoplasm, during vegetative growth","type":"exact"},{"name":"abolished protein localization to medial cortex, with protein mislocalized to cytoplasm during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to medial ring, with protein mislocalized to cytoplasm, during vegetative growth","type":"exact"},{"name":"protein localization to medial cortex abolished, with protein mislocalized to cytoplasm, during vegetative growth","type":"exact"}],"termid":"FYPO:0007027"}


id: PBO:0049397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTSE1 divergent transcript","termid":"PBO:0049397"}


id: PATO:0001349
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A mating type that indicates that the F plasmid has integrated into the chromosome.","definition_xrefs":["MGED:MGED"],"direct_ancestors":[{"relation_name":"is_a","term_name":"F minus mating type","termid":"PATO:0001348"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high frequency recombinant","synonyms":[{"name":"Hfr","type":"exact"}],"termid":"PATO:0001349"}


id: PBO:0074831
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 27","termid":"PBO:0074831"}


id: FYPO:0008099
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the homologous chromosomes do not migrate toward the spindle pole in spindle elongation phase I (anaphase A).","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal homologous chromosome segregation","termid":"FYPO:0004159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000631"],"is_obsolete":false,"name":"abolished homologous chromosome movement at anaphase A","termid":"FYPO:0008099"}


id: GO:0006116
data:
  {"annotated_genes":["SJAG_04152","SJAG_01539","SJAG_00522","SJAG_00409","SJAG_01012"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69875,74293,74529,79613],"is_not":false,"summary":null,"term":"GO:0006116"},{"annotations":[96316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043490"}]},"cv_name":"biological_process","definition":"A metabolic process that results in the oxidation of reduced nicotinamide adenine dinucleotide, NADH, to the oxidized form, NAD+.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NADH metabolic process","termid":"GO:0006734"},{"relation_name":"is_a","term_name":"NAD metabolic process","termid":"GO:0019674"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00409":null,"SJAG_00522":null,"SJAG_01012":null,"SJAG_01539":null,"SJAG_04152":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"NADH oxidation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"NAD (reduced) dehydrogenation","type":"exact"},{"name":"NAD (reduced) oxidation","type":"exact"},{"name":"NADH dehydrogenation","type":"exact"},{"name":"reduced NAD dehydrogenation","type":"exact"},{"name":"reduced NAD oxidation","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide dehydrogenation","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide oxidation","type":"exact"}],"termid":"GO:0006116","terms_by_termid":{"GO:0006116":null,"GO:0043490":null}}


id: PBO:0014273
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUppressor of Cdc2 ts-mutations","termid":"PBO:0014273"}


id: MONDO:0015227
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-syndromic limb malformation (obsolete MONDO:0015227)","secondary_identifiers":["Orphanet:109011"],"synonyms":[{"name":"isolated limb malformation","type":"related"},{"name":"nonsyndromic limb malformation","type":"exact"}],"termid":"MONDO:0015227","xrefs":{"Monarch":{"xref_id":"0015227"}}}


id: PATO:0002112
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's having a hole or holes, especially a row or array of small holes.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure, cavities","termid":"PATO:0002014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"perforate","secondary_identifiers":["PATO:0000649"],"synonyms":[{"name":"permeable","type":"related"},{"name":"pierced","type":"related"}],"termid":"PATO:0002112"}


id: PBO:0075239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 10","termid":"PBO:0075239"}


id: MONDO:0007707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma that involves the small intestine.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"},{"relation_name":"is_a","term_name":"benign neoplasm of small intestine","termid":"MONDO:0021501"}],"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":"hemangiomas of small intestine","secondary_identifiers":["MEDGEN:331098","UMLS:C1841654","MESH:C564201","OMIM:140900"],"synonyms":[{"name":"hemangioma of small intestine","type":"exact"},{"name":"hemangiomas of small intestine","type":"exact"},{"name":"small intestine hemangioma","type":"exact"}],"termid":"MONDO:0007707","xrefs":{"Monarch":{"xref_id":"0007707"}}}


id: MONDO:1010806
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polydactyly that occurs in alpaca.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polydactyly, non-human animal","termid":"MONDO:1010158"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polydactyly, alpaca","secondary_identifiers":["OMIA:000810-30538"],"termid":"MONDO:1010806","xrefs":{"Monarch":{"xref_id":"1010806"}}}


id: MONDO:0002000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial meningitis","termid":"MONDO:0006670"},{"relation_name":"is_a","term_name":"anaerobic bacteria infectious disease","termid":"MONDO:0024389"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaerobic meningitis","secondary_identifiers":["DOID:14559","MEDGEN:678523","SCTID:445059005","ICD9:320.81","UMLS:C0854214"],"synonyms":[{"name":"meningitis caused by anaerobic bacteria","type":"exact"},{"name":"meningitis due to anaerobic bacteria","type":"exact"}],"termid":"MONDO:0002000","xrefs":{"Monarch":{"xref_id":"0002000"}}}


id: PBO:0057702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1289-2","termid":"PBO:0057702"}


id: PBO:0038534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 10, depalmitoylase","termid":"PBO:0038534"}


id: MONDO:0012080
data:
  {"annotated_genes":["SJAG_03815","SJAG_02919","SJAG_04567"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86401,86402,86403],"is_not":false,"summary":null,"term":"MONDO:0012080"}]},"cv_name":"mondo","definition":"Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"distal hereditary motor neuropathy type 2","termid":"MONDO:0015352"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02919":null,"SJAG_03815":null,"SJAG_04567":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0000426","MONDO:0005559"],"is_obsolete":false,"name":"neuronopathy, distal hereditary motor, type 2B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18263","UMLS:C2608087","OMIM:608634","DOID:0111207","MEDGEN:382017","MESH:C567084"],"synonyms":[{"name":"HMN 2B","type":"related"},{"name":"HMN2B","type":"related"},{"name":"HSPB1 neuronopathy, distal hereditary motor","type":"exact"},{"name":"neuronopathy, distal hereditary motor caused by mutation in HSPB1","type":"exact"},{"name":"neuronopathy, distal hereditary motor, type IIB","type":"related"},{"name":"neuropathy, distal hereditary motor, type 2B","type":"related"}],"termid":"MONDO:0012080","terms_by_termid":{"MONDO:0012080":null},"xrefs":{"Monarch":{"xref_id":"0012080"}}}


id: GO:0000131
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the budding yeast plasma membrane where a daughter cell will emerge. The yeast marks this spot with bud-site selection proteins before bud emergence occurs. Actin is polarized to this spot just prior to and during bud emergence.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"site of polarized growth","termid":"GO:0030427"}],"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":"incipient cellular bud site","termid":"GO:0000131"}


id: PBO:0036291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial membrane-associated ribosome receptor Mba1 (predicted)","termid":"PBO:0036291"}


id: PBO:0065841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB9B, member RAS oncogene family","termid":"PBO:0065841"}


id: GO:0031907
data:
  {"annotated_genes":["SJAG_04823","SJAG_00947","SJAG_02630","SJAG_00702","SJAG_00326","SJAG_00706","SJAG_02496"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[111577,70526,105066,114490,115502,118030,111594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005782"}]},"cv_name":"cellular_component","definition":"The volume enclosed by the membranes of a microbody.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular organelle lumen","termid":"GO:0070013"},{"relation_name":"part_of","term_name":"microbody","termid":"GO:0042579"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null,"SJAG_00706":null,"SJAG_00947":null,"SJAG_02496":null,"SJAG_02630":null,"SJAG_04823":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"microbody lumen","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0031907","terms_by_termid":{"GO:0005782":null}}


id: PBO:0003986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis ATPase, Arb family ABCF2-like (predicted)","termid":"PBO:0003986"}


id: MOD:01256
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to 3-methyl-S-(2-sulfanylethyl)cysteine.","definition_xrefs":["PubMed:11507762","Unimod:200#T"],"direct_ancestors":[{"relation_name":"is_a","term_name":"1,2-ethanedithiol modified residue","termid":"MOD:00553"},{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-methyl-S-(2-sulfanylethyl)cysteine (Thr)","synonyms":[{"name":"EDT","type":"related"},{"name":"Ethanedithiol","type":"related"},{"name":"beta-methyl-S-(2-mercaptoethyl)cysteine","type":"exact"}],"termid":"MOD:01256"}


id: PBO:0091298
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae CRD1","termid":"PBO:0091298"}


id: MONDO:0015750
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete amelogenesis imperfecta-gingival hyperplasia syndrome (obsolete MONDO:0015750)","termid":"MONDO:0015750","xrefs":{"Monarch":{"xref_id":"0015750"}}}


id: MONDO:0024662
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm that arises from the glandular epithelium of the colonic and rectal mucosa. It is characterized by tubular and villous architectural patterns. The neoplastic glandular cells have dysplastic features.","definition_xrefs":["NCIT:C5675"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colorectal adenoma","termid":"MONDO:0005484"},{"relation_name":"is_a","term_name":"tubulovillous adenoma","termid":"MONDO:0024661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"colorectal tubulovillous adenoma","secondary_identifiers":["MEDGEN:234165","UMLS:C1333118"],"synonyms":[{"name":"colorectal tubulovillous adenoma","type":"exact"},{"name":"large bowel tubulovillous adenoma","type":"exact"},{"name":"tubulovillous adenoma of large bowel","type":"exact"},{"name":"tubulovillous adenoma of the large bowel","type":"exact"}],"termid":"MONDO:0024662","xrefs":{"Monarch":{"xref_id":"0024662"}}}


id: MONDO:0012469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopia","termid":"MONDO:0001384"}],"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":"myopia 14","secondary_identifiers":["MEDGEN:343990","MESH:C565202","OMIM:610320","UMLS:C1853196"],"synonyms":[{"name":"MYP14","type":"exact"},{"name":"myopia 14","type":"exact"}],"termid":"MONDO:0012469","xrefs":{"Monarch":{"xref_id":"0012469"}}}


id: MONDO:0020555
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pleuropulmonary blastoma composed of malignant small cells. Sarcomatous features are absent.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pleuropulmonary blastoma","termid":"MONDO:0011014"}],"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":"pleuropulmonary blastoma type 1","secondary_identifiers":["Orphanet:99933","SCTID:707671008","UMLS:C1710501","ICD9:162.9","MEDGEN:318288","GARD:19715","NCIT:C45626"],"synonyms":[{"name":"type I pleuropulmonary blastoma","type":"exact"}],"termid":"MONDO:0020555","xrefs":{"Monarch":{"xref_id":"0020555"}}}


id: GO:1905762
data:
  {"annotated_genes":["SJAG_04682","SJAG_02622","SJAG_00686"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89458,104678,117863],"is_not":false,"summary":null,"term":"GO:1905762"}]},"cv_name":"molecular_function","definition":"Binding to a CCR4-NOT complex.","definition_xrefs":["GOC:TermGenie","PMID:26942678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00686":null,"SJAG_02622":null,"SJAG_04682":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":"CCR4-NOT complex binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1905762","terms_by_termid":{"GO:1905762":null}}


id: PBO:0090989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk15","termid":"PBO:0090989"}


id: PBO:0059662
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 28","termid":"PBO:0059662"}


id: PBO:0057855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3166","termid":"PBO:0057855"}


id: PATO:0001309
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A process quality inhering in a bearer by virtue of the bearer's magnitude of the temporal extent between the starting and ending point.","definition_xrefs":["PATOC:mellybelly"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality of a process","termid":"PATO:0002062"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"duration","secondary_identifiers":["PATO:0000081"],"synonyms":[{"name":"period","type":"exact"},{"name":"time","type":"related"}],"termid":"PATO:0001309"}


id: PBO:0049015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycoprotein M6B","termid":"PBO:0049015"}


id: FYPO:0008172
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which acetylation of lysine at position 5 of histone H4 at the silent mating type cassette occurs to a greater extent than normal.","direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H4-K5 acetylation during vegetative growth","termid":"FYPO:0005309"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002274","FYPO:0005447","FYPO:0000002","FYPO:0002494","FYPO:0001985"],"is_obsolete":false,"name":"increased histone H4-K5 acetylation at silent mating-type cassette during vegetative growth","termid":"FYPO:0008172"}


id: PBO:0005537
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 Ssb2","termid":"PBO:0005537"}


id: PBO:0053363
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 272","termid":"PBO:0053363"}


id: GO:0050244
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: CoA + H+ + O2 + pyruvate = acetyl-CoA + CO2 + H2O2.","definition_xrefs":["RHEA:21912"],"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:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"pyruvate oxidase (CoA-acetylating) activity","secondary_identifiers":["EC:1.2.3.6","MetaCyc:PYRUVATE-OXIDASE-COA-ACETYLATING-RXN","KEGG_REACTION:R00211"],"synonyms":[{"name":"pyruvate:oxygen 2-oxidoreductase (CoA-acetylating)","type":"related"}],"termid":"GO:0050244"}


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


id: PBO:0035988
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_eMTOC","termid":"PBO:0035988"}


id: GO:0048853
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the forebrain are generated and organized. The forebrain is the anterior of the three primary divisions of the developing chordate brain or the corresponding part of the adult brain (in vertebrates, includes especially the cerebral hemispheres, the thalamus, and the hypothalamus and especially in higher vertebrates is the main control center for sensory and associative information processing, visceral functions, and voluntary motor functions).","definition_xrefs":["GOC:dph","GOC:cvs","GOC:jid","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"forebrain development","termid":"GO:0030900"},{"relation_name":"part_of","term_name":"brain morphogenesis","termid":"GO:0048854"}],"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":"forebrain morphogenesis","synonyms":[{"name":"prosencephalon morphogenesis","type":"exact"}],"termid":"GO:0048853"}


id: GO:0008854
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the exonucleolytic cleavage (in the presence of ATP) in either 5' to 3' or 3' to 5' direction to yield 5'-phosphooligonucleotides.","definition_xrefs":["EC:3.1.11.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA exonuclease activity, producing 5'-phosphomonoesters","termid":"GO:0016895"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0004527"}],"interesting_parent_ids":["GO:0004527","GO:0003674","GO:0003824","GO:0016788","GO:0016787","GO:0140097"],"is_obsolete":false,"name":"exodeoxyribonuclease V activity","secondary_identifiers":["MetaCyc:RXN0-2605"],"synonyms":[{"name":"E. coli exonuclease V","type":"related"},{"name":"E. coli exonuclease V activity","type":"narrow"},{"name":"Escherichia coli exonuclease V","type":"related"},{"name":"RecBC deoxyribonuclease activity","type":"related"},{"name":"exonuclease V activity","type":"related"},{"name":"gene recBC DNase activity","type":"related"},{"name":"gene recBC endoenzyme","type":"related"},{"name":"gene recBCD enzymes","type":"related"}],"termid":"GO:0008854"}


id: PBO:0030418
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_nucleus_during_cellular_response_to_oxidative_stress","termid":"PBO:0030418"}


id: PBO:0116208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human WDR7 ortholog, implicated vacuolar acidification, autophgy, or vacuole localization","termid":"PBO:0116208"}


id: MONDO:0016883
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosome 1p deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the short arm (p) of chromosome 1. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with chromosome 1p deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. Most cases are not inherited, but people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person.","definition_xrefs":["GARD:0003730"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 1","termid":"MONDO:0016866"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of the short arm of chromosome 1","secondary_identifiers":["MEDGEN:208633","UMLS:C0795796","GARD:3730","Orphanet:261857","icd11.foundation:1004815242","MESH:C535591","NCIT:C36501"],"synonyms":[{"name":"1p deletion","type":"related"},{"name":"1p monosomy","type":"related"},{"name":"chromosome 1p deletion","type":"related"},{"name":"del(1p)","type":"related"},{"name":"deletion 1p","type":"related"},{"name":"loss of chromosome 1p","type":"related"},{"name":"monosomy 1p","type":"related"},{"name":"partial deletion of chromosome 1p","type":"exact"},{"name":"partial deletion of the short arm of chromosome type 1","type":"exact"},{"name":"partial monosomy 1p","type":"related"},{"name":"partial monosomy of chromosome 1p","type":"exact"},{"name":"partial monosomy of the short arm of chromosome 1","type":"exact"}],"termid":"MONDO:0016883","xrefs":{"Monarch":{"xref_id":"0016883"}}}


id: MONDO:0022096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder of the skin, the oral mucosa, and the gingiva, that usually presents as a solitary polypoid capillary hemangioma often resulting from trauma. It is manifested as an inflammatory response with similar characteristics to those of a granuloma.","definition_xrefs":["MESH:D017789"],"direct_ancestors":[{"relation_name":"is_a","term_name":"capillary hemangioma","termid":"MONDO:0002407"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyogenic granuloma","secondary_identifiers":["MEDGEN:39085","UMLS:C0085653","NCIT:C3480","SCTID:200722003"],"synonyms":[{"name":"Capillary Hemangioma, Lobular","type":"related"},{"name":"Capillary hemangioma of granulation tissue type","type":"related"},{"name":"Granulation Tissue-Type Hemangioma","type":"related"},{"name":"Granuloma Pyogenicum","type":"related"},{"name":"Granuloma Telangiecticum","type":"related"},{"name":"Granuloma pyogenicum","type":"related"},{"name":"Granuloma telangiectaticum","type":"related"},{"name":"Granuloma, Pyogenic","type":"related"},{"name":"Granulomata Pyogenicum","type":"related"},{"name":"Lobular Capillary Hemangioma","type":"related"},{"name":"Lobular Hemangioma","type":"related"},{"name":"Lobular capillary hemangioma","type":"related"},{"name":"PG - Pyogenic granuloma","type":"related"},{"name":"Pyogenic Granuloma","type":"related"},{"name":"angiogranuloma","type":"related"},{"name":"angiogranulomas","type":"related"},{"name":"hemangioma, Lobular Capillary","type":"related"},{"name":"hemangiomatous Granulation Tissue","type":"related"}],"termid":"MONDO:0022096","xrefs":{"Monarch":{"xref_id":"0022096"}}}


id: GO:1902033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hematopoietic stem cell proliferation.","definition_xrefs":["GOC:TermGenie","PMID:23403623"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of stem cell proliferation","termid":"GO:0072091"},{"relation_name":"regulates","term_name":"hematopoietic stem cell proliferation","termid":"GO:0071425"}],"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 hematopoietic stem cell proliferation","synonyms":[{"name":"regulation of hemopoietic stem cell proliferation","type":"exact"}],"termid":"GO:1902033"}


id: GO:0035344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of hypoxanthine, 6-hydroxypurine, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleobase transport","termid":"GO:0006863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"hypoxanthine transport","synonyms":[{"name":"6-hydroxypurine transport","type":"exact"},{"name":"hypoxanthine transmembrane transport","type":"exact"}],"termid":"GO:0035344"}


id: GO:1900055
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of leaf senescence.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"leaf senescence","termid":"GO:0010150"}],"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 leaf senescence","termid":"GO:1900055"}


id: GO:1903688
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of border follicle cell migration.","definition_xrefs":["GOC:als","GOC:TermGenie","PMID:18394891","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of epithelial cell migration","termid":"GO:0010634"},{"relation_name":"is_a","term_name":"regulation of border follicle cell migration","termid":"GO:1903684"},{"relation_name":"positively_regulates","term_name":"border follicle cell migration","termid":"GO:0007298"}],"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 border follicle cell migration","synonyms":[{"name":"activation of border follicle cell migration","type":"narrow"}],"termid":"GO:1903688"}


id: PBO:0050898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon alpha inducible protein 6","termid":"PBO:0050898"}


id: PR:Q9UT10
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ski7 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UT10"],"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 GTP-binding protein P8A3.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP8A3.05","synonyms":[{"name":"Spom972h-ski7","type":"exact"}],"termid":"PR:Q9UT10"}


id: GO:0071908
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Determination of the asymmetric location of the intestine loops with respect to the left and right halves of the organism.","definition_xrefs":["GOC:cvs"],"direct_ancestors":[{"relation_name":"is_a","term_name":"determination of digestive tract left/right asymmetry","termid":"GO:0071907"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"determination of intestine left/right asymmetry","termid":"GO:0071908"}


id: MONDO:0003088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma arising from skeletal muscle.","definition_xrefs":["NCIT:C3699"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deep hemangioma","termid":"MONDO:0003096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intramuscular hemangioma","secondary_identifiers":["UMLS:C0205789","ICDO:9132/0","MEDGEN:61450","DOID:468"],"synonyms":[{"name":"intramuscular angioma","type":"exact"},{"name":"intramuscular hemangioma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003088","xrefs":{"Monarch":{"xref_id":"0003088"}}}


id: GO:0010775
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which double strand breaks are formed and repaired through a double Holliday junction intermediate resulting in meiotic recombination.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic strand invasion","termid":"GO:0000708"},{"relation_name":"part_of","term_name":"meiotic gene conversion","termid":"GO:0006311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006310","GO:0006259","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"meiotic strand invasion involved in meiotic gene conversion","termid":"GO:0010775"}


id: GO:0010645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell communication via chemical coupling. Cell communication by chemical coupling is the process that mediates signaling interactions between one cell and another cell by the transfer of small, water-soluble molecules or metabolites between their adjacent cytoplasms via intercellular protein channels.","definition_xrefs":["GOC:dph","GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication","termid":"GO:0010646"},{"relation_name":"regulates","term_name":"cell communication by chemical coupling","termid":"GO:0010643"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell communication by chemical coupling","termid":"GO:0010645"}


id: MONDO:0006392
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A serrated polypoid lesion that arises in the rectum. It rarely produces symptoms. This group includes goblet cell rich, mucin poor, and microvesicular hyperplastic polyps.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyp of rectum","termid":"MONDO:0021398"}],"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":"rectal hyperplastic polyp","secondary_identifiers":["MEDGEN:277574","UMLS:C1335679","NCIT:C5619","EFO:1000502"],"synonyms":[{"name":"hyperplastic polyp of rectum","type":"exact"},{"name":"hyperplastic polyp of the rectum","type":"exact"},{"name":"rectal Hp","type":"exact"},{"name":"rectal MP","type":"exact"},{"name":"rectal metaplastic polyp","type":"exact"}],"termid":"MONDO:0006392","xrefs":{"Monarch":{"xref_id":"0006392"}}}


id: MONDO:0012370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 11p13-p12.","definition_xrefs":["DOID:0110508","PMID:16158433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 51","secondary_identifiers":["OMIM:609941","UMLS:C1864968","MEDGEN:355880","GARD:9918","MESH:C538202"],"synonyms":[{"name":"DFNB51","type":"narrow"},{"name":"autosomal recessive deafness 51","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 51","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 51","type":"narrow"},{"name":"deafness, autosomal recessive 51","type":"narrow"}],"termid":"MONDO:0012370","xrefs":{"Monarch":{"xref_id":"0012370"}}}


id: PBO:0046487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expanded repeat domain, CAG/CTG 1","termid":"PBO:0046487"}


id: PBO:0087576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the 26S proteasome; substrate of the N-acetyltransferase Nat1p; protein abundance increases in response to DNA replication stress","termid":"PBO:0087576"}


id: GO:1901614
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of terminal button organization.","definition_xrefs":["GOC:TermGenie","PMID:22426000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of terminal button organization","termid":"GO:2000331"},{"relation_name":"positively_regulates","term_name":"terminal button organization","termid":"GO:0072553"}],"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 terminal button organization","synonyms":[{"name":"activation of bouton organization","type":"narrow"},{"name":"activation of presynaptic bouton organization","type":"narrow"},{"name":"activation of synaptic bouton organization","type":"narrow"},{"name":"activation of terminal bouton organization","type":"narrow"},{"name":"activation of terminal button organisation","type":"narrow"},{"name":"activation of terminal button organization","type":"narrow"},{"name":"positive regulation of bouton organization","type":"exact"},{"name":"positive regulation of presynaptic bouton organization","type":"exact"},{"name":"positive regulation of synaptic bouton organization","type":"exact"},{"name":"positive regulation of terminal bouton organization","type":"exact"},{"name":"positive regulation of terminal button organisation","type":"exact"},{"name":"up regulation of bouton organization","type":"exact"},{"name":"up regulation of presynaptic bouton organization","type":"exact"},{"name":"up regulation of synaptic bouton organization","type":"exact"},{"name":"up regulation of terminal bouton organization","type":"exact"},{"name":"up regulation of terminal button organisation","type":"exact"},{"name":"up regulation of terminal button organization","type":"exact"},{"name":"up-regulation of bouton organization","type":"exact"},{"name":"up-regulation of presynaptic bouton organization","type":"exact"},{"name":"up-regulation of synaptic bouton organization","type":"exact"},{"name":"up-regulation of terminal bouton organization","type":"exact"},{"name":"up-regulation of terminal button organisation","type":"exact"},{"name":"up-regulation of terminal button organization","type":"exact"},{"name":"upregulation of bouton organization","type":"exact"},{"name":"upregulation of presynaptic bouton organization","type":"exact"},{"name":"upregulation of synaptic bouton organization","type":"exact"},{"name":"upregulation of terminal bouton organization","type":"exact"},{"name":"upregulation of terminal button organisation","type":"exact"},{"name":"upregulation of terminal button organization","type":"exact"}],"termid":"GO:1901614"}


id: PBO:0051706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol polyphosphate-5-phosphatase F","termid":"PBO:0051706"}


id: PBO:0072319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 5","termid":"PBO:0072319"}


id: PBO:0090670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial CH-OH group oxidoreductase, human RTN4IP1 ortholog, implicated in mitochondrial organization or tethering","termid":"PBO:0090670"}


id: GO:0050558
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-maltose = beta-maltose.","definition_xrefs":["RHEA:21228","EC:5.1.3.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on carbohydrates and derivatives","termid":"GO:0016857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"maltose epimerase activity","secondary_identifiers":["KEGG_REACTION:R07319","MetaCyc:5.1.3.21-RXN"],"synonyms":[{"name":"maltose 1-epimerase activity","type":"related"}],"termid":"GO:0050558"}


id: GO:0009494
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete chloroplast-type ferredoxin (obsolete GO:0009494)","synonyms":[{"name":"chloroplast-type ferredoxin","type":"exact"}],"termid":"GO:0009494"}


id: MONDO:0011236
data:
  {"annotated_genes":["SJAG_04495","SJAG_04334"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86264,86265],"is_not":false,"summary":null,"term":"MONDO:0011236"}]},"cv_name":"mondo","definition":"Hyperinsulism due to glucokinase deficiency (HIGCK) is a form of diazoxide-sensitive diffuse hyperinsulinism, caused by a lowered threshold for insulin release, characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia) and recurrent episodes of profound hypoglycemia induced by fasting and protein rich meals, requiring rapid and intensive treatment to prevent neurological sequelae.","definition_xrefs":["Orphanet:79299"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diazoxide-sensitive diffuse hyperinsulinism","termid":"MONDO:0015624"},{"relation_name":"is_a","term_name":"disorder of glycolysis","termid":"MONDO:0017688"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04334":null,"SJAG_04495":null},"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"},{"rel_name":"is_a","termid":"MONDO:0019254"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0004335","MONDO:0019254"],"is_obsolete":false,"name":"hyperinsulinism due to glucokinase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:2818","DOID:0070216","MEDGEN:355435","OMIM:602485","SCTID:717182006","MESH:C538374","UMLS:C1865290"],"synonyms":[{"name":"HHF3","type":"related"},{"name":"hyperinsulinemic hypoglycemia due to glucokinase deficiency","type":"exact"},{"name":"hyperinsulinemic hypoglycemia familial 3","type":"related"},{"name":"hyperinsulinemic hypoglycemia, familial, 3","type":"related"},{"name":"hyperinsulinemic hypoglycemia, familial, type 3","type":"exact"}],"termid":"MONDO:0011236","terms_by_termid":{"MONDO:0011236":null},"xrefs":{"Monarch":{"xref_id":"0011236"}}}


id: PBO:0056220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member C3","termid":"PBO:0056220"}


id: GO:0102648
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: D-fructose 6-phosphate + D-ribose 5-phosphate = D-glycero-D-altro-octulose 8-phosphate + D-glyceraldehyde 3-phosphate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete D-ribose 5-phosphate:D-fructose 6-phosphate transaldolase activity (obsolete GO:0102648)","termid":"GO:0102648"}


id: PBO:0053809
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 1068","termid":"PBO:0053809"}


id: GO:1900358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of nigerotriose transport.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"regulation of nigerotriose transport","termid":"GO:1900357"},{"relation_name":"negatively_regulates","term_name":"nigerotriose transport","termid":"GO:2001091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of nigerotriose transport","synonyms":[{"name":"down regulation of nigerotriose transport","type":"exact"},{"name":"down-regulation of nigerotriose transport","type":"exact"},{"name":"downregulation of nigerotriose transport","type":"exact"},{"name":"inhibition of nigerotriose transport","type":"narrow"}],"termid":"GO:1900358"}


id: MONDO:0001699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dermatophytosis that involves the hands.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatophytosis","termid":"MONDO:0004678"}],"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":"tinea manuum","secondary_identifiers":["DOID:13369","ICD10CM:B35.2","SCTID:48971001","UMLS:C0153246","MEDGEN:509222","ICD9:110.2"],"synonyms":[{"name":"Tinea manus","type":"exact"},{"name":"dermatophytosis of hand","type":"exact"},{"name":"dermatophytosis of manus","type":"exact"},{"name":"manus dermatophytosis","type":"exact"}],"termid":"MONDO:0001699","xrefs":{"Monarch":{"xref_id":"0001699"}}}


id: PBO:0048990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glypican 2","termid":"PBO:0048990"}


id: GO:0090250
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of one cell to another cell via adhesion molecules that contributes to the establishment of planar cell polarity.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion via plasma-membrane adhesion molecules","termid":"GO:0098742"},{"relation_name":"part_of","term_name":"establishment of planar polarity","termid":"GO:0001736"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"cell-cell adhesion involved in establishment of planar polarity","termid":"GO:0090250"}


id: GO:0097504
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Nuclear bodies frequently found near or associated with Cajal bodies (also called coiled bodies or CBs). Gemini of coiled bodies, or 'gems', are similar in size and shape to CBs, and often indistinguishable under the microscope. Unlike CBs, gems do not contain small nuclear ribonucleoproteins (snRNPs); they contain a protein called survivor of motor neurons (SMN) whose function relates to snRNP biogenesis. Gems are believed to assist CBs in snRNP biogenesis, and to play a role in the etiology of spinal muscular atrophy (SMA).","definition_xrefs":["Wikipedia:Cell_nucleus#Cajal_bodies_and_gems","GOC:pr","PMID:11031238","PMID:9683623"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear body","termid":"GO:0016604"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005654","GO:0005634"],"is_obsolete":false,"name":"Gemini of Cajal bodies","synonyms":[{"name":"Gemini of coiled bodies","type":"exact"},{"name":"Gems","type":"exact"}],"termid":"GO:0097504"}


id: PBO:0057643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1234","termid":"PBO:0057643"}


id: PBO:0030046
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_ferrous_iron_import","termid":"PBO:0030046"}


id: MONDO:0043576
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the arterial intima.","definition_xrefs":["NCIT:C34581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arteritis","termid":"MONDO:0043494"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endarteritis","secondary_identifiers":["MESH:D004692","UMLS:C0014100","MEDGEN:41777","SCTID:33806008"],"synonyms":[{"name":"Endarteritides","type":"related"},{"name":"endarteritis","type":"exact"},{"name":"inflammation of tunica intima of artery","type":"exact"},{"name":"tunica intima of artery inflammation","type":"exact"}],"termid":"MONDO:0043576","xrefs":{"Monarch":{"xref_id":"0043576"}}}


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


id: GO:0055002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a striated muscle cell over time, from its formation to the mature structure. Striated muscle cells contain fibers that are divided by transverse bands into striations, and cardiac and skeletal muscle are types of striated muscle.","definition_xrefs":["GOC:devbiol","CL:0000737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle cell development","termid":"GO:0055001"},{"relation_name":"part_of","term_name":"striated muscle cell differentiation","termid":"GO:0051146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"striated muscle cell development","termid":"GO:0055002"}


id: GO:0035325
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a Toll-like protein, a pattern recognition receptor that binds pattern motifs from a variety of microbial sources to initiate an innate immune response.","definition_xrefs":["PMID:19076341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"Toll-like receptor binding","synonyms":[{"name":"TLR binding","type":"exact"}],"termid":"GO:0035325"}


id: MONDO:0043009
data:
  {"annotated_genes":["SJAG_00773","SJAG_02712","SJAG_03557"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85240,85241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012980"},{"annotations":[85197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014552"}]},"cv_name":"mondo","definition":"An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00773":null,"SJAG_02712":null,"SJAG_03557":null},"genotype_count":0,"is_obsolete":false,"name":"hereditary lethal multiple congenital anomalies/dysmorphic syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:21947","Orphanet:471383","MEDGEN:1843298","UMLS:C5681265"],"synonyms":[{"name":"genetic lethal multiple congenital anomalies/dysmorphic syndrome","type":"exact"}],"termid":"MONDO:0043009","terms_by_termid":{"MONDO:0012980":null,"MONDO:0014552":null},"xrefs":{"Monarch":{"xref_id":"0043009"}}}


id: MONDO:0014157
data:
  {"annotated_genes":["SJAG_02818"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85728],"is_not":false,"summary":null,"term":"MONDO:0014157"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"progeroid syndrome","termid":"MONDO:0015333"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"premature aging syndrome","termid":"MONDO:0019303"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02818":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0019303"],"is_obsolete":false,"name":"mandibular hypoplasia-deafness-progeroid syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3715192","MEDGEN:811623","OMIM:615381","GARD:10989","Orphanet:363649"],"synonyms":[{"name":"MDP syndrome","type":"exact"},{"name":"MDPL","type":"related"},{"name":"mandibular hypoplasia, deafness, progeroid features","type":"related"},{"name":"mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome","type":"related"},{"name":"mandibular hypoplasia-hearing loss-progeroid syndrome","type":"exact"}],"termid":"MONDO:0014157","terms_by_termid":{"MONDO:0014157":null},"xrefs":{"Monarch":{"xref_id":"0014157"}}}


id: MONDO:0005950
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Poisoning caused by ingestion of food harboring species of salmonella. Conditions of raising, shipping, slaughtering, and marketing of domestic animals contribute to the spread of this bacterium in the food supply.","definition_xrefs":["MESH:D012478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salmonellosis","termid":"MONDO:0000827"},{"relation_name":"is_a","term_name":"gastroenteritis","termid":"MONDO:0002269"},{"relation_name":"is_a","term_name":"digestive system infectious disorder","termid":"MONDO:0043424"}],"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":"Salmonella gastroenteritis","secondary_identifiers":["UMLS:C0036114","MEDGEN:48541","EFO:0007475","SCTID:42338000","ICD9:003.0"],"synonyms":[{"name":"Salmonella caused gastroenteritis","type":"exact"}],"termid":"MONDO:0005950","xrefs":{"Monarch":{"xref_id":"0005950"}}}


id: PBO:0089086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane copper transporter complex subunit Ctr5","termid":"PBO:0089086"}


id: PBO:0068591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 42, pseudogene","termid":"PBO:0068591"}


id: PBO:0035858
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H2A_phosphorylation_during_vegetative_growth","termid":"PBO:0035858"}


id: PBO:0003156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfiredoxin","termid":"PBO:0003156"}


id: FYPO:0003679
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to epirubicin. Cells stop growing (and may die) at a concentration of epirubicin 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:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0002683","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to epirubicin","synonyms":[{"name":"hypersensitive to epirubicin","type":"exact"},{"name":"sensitive to 4'-epidoxorubicin","type":"exact"},{"name":"sensitive to epirubicin during mitotic cell cycle","type":"related"},{"name":"sensitive to epirubicin during vegetative growth","type":"exact"}],"termid":"FYPO:0003679"}


id: GO:1903498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a bundle sheath cell.","definition_xrefs":["GOC:TermGenie","GOC:tb","GO_REF:0000086","PMID:24517883"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"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":"bundle sheath cell differentiation","termid":"GO:1903498"}


id: PBO:0058940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanocyte inducing transcription factor","termid":"PBO:0058940"}


id: GO:0072366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of a cellular ketone metabolic process by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:BHF","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular ketone metabolic process by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:0072366)","synonyms":[{"name":"regulation of cellular ketone metabolic process by positive regulation of transcription from an RNA polymerase II promoter","type":"exact"},{"name":"regulation of cellular ketone metabolism by positive regulation of transcription from an RNA polymerase II promoter","type":"exact"}],"termid":"GO:0072366"}


id: PBO:0004209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3, MARCH family (predicted)","termid":"PBO:0004209"}


id: GO:0007342
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 single fertilization. In sperm with flagella, binding occurs at the posterior (post-acrosomal) region of the sperm head.","definition_xrefs":["GOC:jl","PMID:17644969","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":"single fertilization","termid":"GO:0007338"}],"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":"fusion of sperm to egg plasma membrane involved in single fertilization","synonyms":[{"name":"sperm-oocyte fusion","type":"narrow"}],"termid":"GO:0007342"}


id: PBO:0017921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial FAD transmembrane transporter (predicted)","termid":"PBO:0017921"}


id: PBO:0041329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 83","termid":"PBO:0041329"}


id: GO:1902201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of bacterial-type flagellum-dependent cell motility.","definition_xrefs":["GOC:TermGenie","GOC:jl","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of bacterial-type flagellum-dependent cell motility","termid":"GO:1902021"},{"relation_name":"is_a","term_name":"negative regulation of cell motility","termid":"GO:2000146"},{"relation_name":"negatively_regulates","term_name":"bacterial-type flagellum-dependent cell motility","termid":"GO:0071973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of bacterial-type flagellum-dependent cell motility","synonyms":[{"name":"down regulation of bacterial-type flagellar cell motility","type":"exact"},{"name":"down regulation of flagellin-based flagellar cell motility","type":"exact"},{"name":"down-regulation of bacterial-type flagellar cell motility","type":"exact"},{"name":"down-regulation of flagellin-based flagellar cell motility","type":"exact"},{"name":"downregulation of bacterial-type flagellar cell motility","type":"exact"},{"name":"downregulation of flagellin-based flagellar cell motility","type":"exact"},{"name":"inhibition of bacterial-type flagellar cell motility","type":"narrow"},{"name":"inhibition of flagellin-based flagellar cell motility","type":"exact"},{"name":"negative regulation of bacterial-type flagellar cell motility","type":"related"},{"name":"negative regulation of flagellin-based flagellar cell motility","type":"exact"}],"termid":"GO:1902201"}


id: MONDO:0016839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal 17p13.3 microdeletion syndrome is a rare partial monosomy of the short arm of chromosome 17 with a variable phenotype characterized by prenatal and postnatal growth retardation, developmental delay, mild intellectual disability, macrocephaly, mild facial dysmorphisms including prominent forehead, hypertelorism, thick upper and/or lower lip vermillion, and structural abnormalities of the brain variably including white matter abnormalities, prominent Virchow-Robin spaces, Chiari I malformation, corpus callosum hypoplasia, but no lissencephaly.","definition_xrefs":["Orphanet:261257"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 17p deletion","termid":"MONDO:0022754"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal 17p13.3 microdeletion syndrome","secondary_identifiers":["UMLS:C4707092","SCTID:764696007","GARD:20776","MEDGEN:1643975"],"synonyms":[{"name":"distal del(17)(p13.3)","type":"exact"},{"name":"distal monosomy 17p13.3","type":"exact"}],"termid":"MONDO:0016839","xrefs":{"Monarch":{"xref_id":"0016839"}}}


id: GO:0043008
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a protein or protein complex using energy from ATP hydrolysis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"ATP-dependent protein binding","termid":"GO:0043008"}


id: PBO:0113448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of a TORC1-stimulating GTPase and the EGO/GSE complex; subunit of Gtr1-Gtr2, a GTPase that activates TORC1 in response to amino acid stimulation; negatively regulates the GTPase cycle of Gtr1p, a Ran/TC4 homolog; subunit of EGO, a vacuolar membrane complex that regulates exit from rapamycin-induced growth arrest and esorting of Gap1p; activates transcription when chromatin bound; role in the oxidative stress response; activated by the Lst4p-Lst7p GAP complex; homolog of human RagC","termid":"PBO:0113448"}


id: PBO:0084151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-affinity nicotinamide riboside transporter; also transports thiamine with low affinity; major transporter for 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (acadesine) uptake; shares sequence similarity with Thi7p and Thi72p; proposed to be involved in 5-fluorocytosine sensitivity","termid":"PBO:0084151"}


id: GO:0060279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ovulation, the release of a mature ovum/oocyte from an ovary.","definition_xrefs":["GOC:dph","GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of ovulation","termid":"GO:0060278"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"ovulation","termid":"GO:0030728"}],"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 ovulation","termid":"GO:0060279"}


id: PBO:0014298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S. pombe specific family","termid":"PBO:0014298"}


id: GO:0060897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pattern specification process that results in the subdivision of an axis or axes of the neural plate in space to define an area or volume in which specific patterns of cell differentiation will take place or in which cells interpret a specific environment.","definition_xrefs":["GOC:sdb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"is_a","term_name":"neural plate pattern specification","termid":"GO:0060896"}],"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 plate regionalization","termid":"GO:0060897"}


id: GO:0060390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of SMAD protein signal transduction.","definition_xrefs":["GOC:dph","GOC:tb","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"SMAD protein signal transduction","termid":"GO:0060395"}],"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:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of SMAD protein signal transduction","secondary_identifiers":["GO:0007184"],"synonyms":[{"name":"SMAD protein import into nucleus","type":"narrow"},{"name":"regulation of SMAD protein nuclear translocation","type":"narrow"}],"termid":"GO:0060390"}


id: GO:0140398
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalyzes the reaction: versicolorin B + NADPH + O2 = versicolorin A + NADP+ + 2 H2O. Uses heme-thiolate as a co-factor. Involved in the synthesis of aflatoxins in the fungus Aspergillus parasiticus.","definition_xrefs":["PMID:15006741","PMID:8368837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water","termid":"GO:0016717"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"versicolorin B desaturase activity","secondary_identifiers":["EC:1.14.19.n5","KEGG_REACTION:R10479","RHEA:35743","MetaCyc:RXN-9495"],"termid":"GO:0140398"}


id: PBO:0083448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene BUD31","termid":"PBO:0083448"}


id: PATO:0001690
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A contractility quality inhering in a bearer by virtue of the bearer's ability of contracting or being contracted.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"contractility","termid":"PATO:0001579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contractile","termid":"PATO:0001690"}


id: PBO:0053139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactate dehydrogenase A like 6A","termid":"PBO:0053139"}


id: MONDO:0045055
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma characterized by the presence of malignant epithelial cells with abundant clear cytoplasm which contains glycogen. A representative example is the glycogen-rich, clear cell breast carcinoma.","definition_xrefs":["NCIT:C4153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"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":"glycogen-rich carcinoma","secondary_identifiers":["DOID:0081028","MEDGEN:83127","UMLS:C0334319"],"synonyms":[{"name":"Glycogen-rich carcinoma","type":"exact"}],"termid":"MONDO:0045055","xrefs":{"Monarch":{"xref_id":"0045055"}}}


id: GO:0018135
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-cysteine cyclase activity (obsolete GO:0018135)","synonyms":[{"name":"peptidyl-cysteine cyclase activity","type":"exact"}],"termid":"GO:0018135"}


id: MONDO:0025095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any of a group of infections of fowl caused by protozoa of the genera plasmodium, Leucocytozoon, and Haemoproteus. The life cycles of these parasites and the disease produced bears strong resemblance to those observed in human malaria.","definition_xrefs":["MESH:D008289"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"protozoan infections, animal","termid":"MONDO:0025114"},{"relation_name":"is_a","term_name":"vector-borne disease, non-human animal","termid":"MONDO:0700114"},{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malaria, avian","synonyms":[{"name":"Avian Malarias","type":"related"},{"name":"Avian malaria","type":"related"},{"name":"Malarias, Avian","type":"related"}],"termid":"MONDO:0025095","xrefs":{"Monarch":{"xref_id":"0025095"}}}


id: MONDO:0017069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital abnormality in which the spinal cord and meninges protrude through a defect in the spinal column. The protrusion is above the skin surface.","definition_xrefs":["NCIT:C101201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated spina bifida","termid":"MONDO:0019351"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"spina bifida cystica","secondary_identifiers":["MedDRA:10071011","icd11.foundation:979482551","MEDGEN:21277","MESH:D016137","NANDO:2200814","Orphanet:268744","UMLS:C0037917","NANDO:1200509","GARD:20958","NANDO:2100215"],"synonyms":[{"name":"meningomyelocele","type":"exact"},{"name":"myelomeningocele","type":"narrow"},{"name":"open spina bifida","type":"related"},{"name":"spina bifida aperta","type":"related"},{"name":"spina bifida manifesta","type":"related"},{"name":"spina bifida, open","type":"related"}],"termid":"MONDO:0017069","xrefs":{"Monarch":{"xref_id":"0017069"}}}


id: PBO:0079216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thiosulfate sulfurtransferase like domain containing 1","termid":"PBO:0079216"}


id: PBO:0061643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUDT19 pseudogene 1","termid":"PBO:0061643"}


id: MONDO:0011194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset autosomal dominant Alzheimer disease","termid":"MONDO:0015140"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"Alzheimer disease 5","secondary_identifiers":["MESH:C566578","GARD:16507","OMIM:602096","DOID:0110037","MEDGEN:356103","UMLS:C1865868"],"synonyms":[{"name":"AD5","type":"exact"},{"name":"Ad5","type":"related"},{"name":"Alzheimer disease 5","type":"exact"},{"name":"Alzheimer disease type 5","type":"exact"},{"name":"Alzheimer disease, familial 5","type":"exact"},{"name":"Alzheimer disease, familial, 5","type":"related"},{"name":"Alzheimer disease-5","type":"exact"},{"name":"Alzheimer's disease 5","type":"related"},{"name":"Alzheimer's disease type 5","type":"exact"}],"termid":"MONDO:0011194","xrefs":{"Monarch":{"xref_id":"0011194"}}}


id: MONDO:0015872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete giant adenofibroma of the breast (obsolete MONDO:0015872)","termid":"MONDO:0015872","xrefs":{"Monarch":{"xref_id":"0015872"}}}


id: PBO:0073593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SHOC2 leucine rich repeat scaffold protein","termid":"PBO:0073593"}


id: PBO:0081254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF24 transcription regulator","termid":"PBO:0081254"}


id: GO:1990465
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction a long-chain aldehyde + O2 + 2 NADPH = an alkane + formate + H2O + 2 NADP+.","definition_xrefs":["GOC:mengo_curators","PMID:22947199"],"gene_count":0,"genotype_count":0,"name":"obsolete aldehyde oxygenase (deformylating) activity (obsolete GO:1990465)","termid":"GO:1990465"}


id: PBO:0054181
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 1555","termid":"PBO:0054181"}


id: GO:0035951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of oligopeptide transport by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:dgf"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of oligopeptide transport by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:0035951)","synonyms":[{"name":"positive regulation of oligopeptide transport by activation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of oligopeptide transport by positive regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of oligopeptide transport by stimulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of oligopeptide transport by up regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of oligopeptide transport by up-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of oligopeptide transport by upregulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:0035951"}


id: GO:0008973
data:
  {"annotated_genes":["SJAG_00134"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73296],"is_not":false,"summary":null,"term":"GO:0008973"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribose 1-phosphate = D-ribose 5-phosphate. Also converts 2-deoxy-alpha-D-ribose 1-phosphate into 2-deoxy-D-ribose 5-phosphate.","definition_xrefs":["EC:5.4.2.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular phosphotransferase activity","termid":"GO:0016868"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00134":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"phosphopentomutase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:PPENTOMUT-RXN","Reactome:R-HSA-8982667","Reactome:R-HSA-6787329"],"synonyms":[{"name":"D-ribose 1,5-phosphomutase activity","type":"related"},{"name":"alpha-D-glucose-1,6-bisphosphate:deoxy-D-ribose-1-phosphate phosphotransferase activity","type":"related"},{"name":"alpha-D-ribose 1,5-phosphomutase activity","type":"related"},{"name":"deoxyribomutase activity","type":"related"},{"name":"deoxyribose phosphomutase activity","type":"related"},{"name":"phosphodeoxyribomutase activity","type":"related"},{"name":"phosphoribomutase activity","type":"related"}],"termid":"GO:0008973","terms_by_termid":{"GO:0008973":null}}


id: PBO:0030467
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_pantothenate_import","termid":"PBO:0030467"}


id: MOD:00212
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-4-hydroxycinnamyl-L-cysteine.","definition_xrefs":["PubMed:7947803","RESID:AA0207","Unimod:407","PubMed:7981196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-4-hydroxycinnamyl-L-cysteine","synonyms":[{"name":"(2R)-2-amino-3-([(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]sulfanyl)propanoic acid","type":"exact"},{"name":"Hydroxycinnamyl","type":"related"},{"name":"MOD_RES S-(4-hydroxycinnamyl)cysteine","type":"exact"},{"name":"S-4-hydroxycinnamyl-L-cysteine","type":"exact"},{"name":"S-para-coumaryl-L-cysteine","type":"exact"},{"name":"cinnamate cysteine thioester","type":"exact"},{"name":"hydroxycinnamyl","type":"related"}],"termid":"MOD:00212"}


id: SO:0000092
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene from chloroplast sequence.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"chloroplast_sequence","termid":"SO:0000745"},{"relation_name":"is_a","term_name":"plastid_gene","termid":"SO:0000090"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ct_gene","synonyms":[{"name":"chloroplast gene","type":"exact"},{"name":"ct gene","type":"exact"}],"termid":"SO:0000092"}


id: MONDO:1011325
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Immunodeficiency-Related disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunodeficiency-related disorder, non-human animal","termid":"MONDO:1011325","xrefs":{"Monarch":{"xref_id":"1011325"}}}


id: GO:0004935
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with epinephrine or norepinephrine and transmitting the signal across the membrane by activating the alpha-subunit of an associated heterotrimeric G-protein complex.","definition_xrefs":["GOC:bf","GOC:mah","IUPHAR_GPCR:1274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled amine receptor activity","termid":"GO:0008227"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"adrenergic receptor activity","secondary_identifiers":["Wikipedia:Adrenergic_receptor"],"synonyms":[{"name":"adrenoceptor activity","type":"exact"}],"termid":"GO:0004935"}


id: PBO:0077259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane p24 trafficking protein 9","termid":"PBO:0077259"}


id: MONDO:0001847
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A senile cataract that involves the lens nucleus.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"senile cataract","termid":"MONDO:0004847"},{"relation_name":"is_a","term_name":"nuclear cataract","termid":"MONDO:0045050"}],"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":"nuclear senile cataract","secondary_identifiers":["UMLS:C0271166","DOID:13963","ICD9:366.16","SCTID:193589009","MEDGEN:543204"],"synonyms":[{"name":"Senile nuclear cataract","type":"exact"},{"name":"Senile nuclear sclerosis","type":"exact"},{"name":"lens nucleus senile cataract","type":"exact"},{"name":"senile cataract of lens nucleus","type":"exact"}],"termid":"MONDO:0001847","xrefs":{"Monarch":{"xref_id":"0001847"}}}


id: GO:0015185
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of gamma-aminobutyric acid from one side of a membrane to the other. Gamma-aminobutyric acid is 4-aminobutyrate (GABA).","definition_xrefs":["ISBN:0198506732","GOC:mtg_transport","GOC:go_curators","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transmembrane transporter activity","termid":"GO:0008028"},{"relation_name":"is_a","term_name":"amino acid transmembrane transporter activity","termid":"GO:0015171"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"gamma-aminobutyric acid transmembrane transporter activity","synonyms":[{"name":"4-aminobutanoate transporter activity","type":"exact"},{"name":"4-aminobutyrate transporter activity","type":"exact"},{"name":"GABA transporter activity","type":"exact"},{"name":"betaine/GABA:sodium symporter activity","type":"narrow"}],"termid":"GO:0015185"}


id: FYPO:0003762
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the mitotic cell cycle spindle assembly checkpoint is normal (i.e. indistinguishable from wild type). The mitotic spindle assembly checkpoint normally delays the metaphase/anaphase transition of a mitotic nuclear division until the spindle is correctly assembled and chromosomes are attached to the spindle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic cell cycle checkpoint","termid":"FYPO:0001703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001312","FYPO:0000298","FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal mitotic spindle assembly checkpoint","synonyms":[{"name":"normal mitotic cell cycle spindle assembly checkpoint","type":"exact"},{"name":"normal mitotic spindle assembly checkpoint activation","type":"related"},{"name":"normal spindle assembly checkpoint during mitotic cell cycle","type":"exact"},{"name":"normal spindle assembly checkpoint during vegetative growth","type":"exact"}],"termid":"FYPO:0003762"}


id: PBO:0045221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJC9 and MRPS16 antisense RNA 1","termid":"PBO:0045221"}


id: PBO:0048721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutaminase","termid":"PBO:0048721"}


id: PBO:0049695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan and proteoglycan link protein 1","termid":"PBO:0049695"}


id: FYPO:0000304
data:
  {"alleles_by_uniquename":{"SJAG_00266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00266","name":"atf1delta","uniquename":"SJAG_00266:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_04312:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04312","name":"pka1delta","uniquename":"SJAG_04312:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000087"},{"annotations":[119063,119051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000726"},{"annotations":[119050,119062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000271"}]},"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 a stress. Typically, a cell population is deemed sensitive to a stress if cells in the population stop growing (and may die) when exposed to the stress at an intensity that allows a population of wild type cells to grow and divide.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vegetative cell population growth phenotype","termid":"FYPO:0001358"},{"relation_name":"is_a","term_name":"sensitive to stress","termid":"FYPO:0002549"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_02592":null,"SJAG_04312":null},"genotype_count":3,"genotypes_by_uniquename":{"atf1delta":{"display_name":"atf1delta","display_uniquename":"atf1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00266:allele-1","expression":"Null"}]}]},"pka1delta":{"display_name":"pka1delta","display_uniquename":"pka1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04312:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to stress during vegetative growth","references_by_uniquename":{"PMID:27678009":null,"PMID:31150379":null},"single_locus_annotated_genes":["SJAG_00266","SJAG_02592","SJAG_04312"],"single_locus_genotype_uniquenames":["atf1delta","sty1delta","pka1delta"],"synonyms":[{"name":"decreased growth during cellular response to stress during vegetative growth","type":"exact"},{"name":"decreased vegetative cell population growth during cellular response to stress during vegetative growth","type":"exact"},{"name":"hypersensitive to stress during vegetative growth","type":"exact"},{"name":"sensitive to stress during mitotic cell cycle","type":"related"},{"name":"stress resistance: decreased during vegetative growth","type":"related"}],"termid":"FYPO:0000304","terms_by_termid":{"FYECO:0000078":null,"FYECO:0000207":null,"FYPO:0000087":null,"FYPO:0000271":null,"FYPO:0000726":null,"FYPO_EXT:0000001":null}}


id: MONDO:0005823
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any disease caused by Legionella bacteria.","definition_xrefs":["NCIT:C128334"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"legionellosis","secondary_identifiers":["UMLS:C0023240","MESH:D007876","SCTID:26726000","GARD:22419","icd11.foundation:424434722","DOID:10458","Orphanet:549","MedDRA:10035718","MEDGEN:7292","MedDRA:10061266","EFO:0007342","icd11.foundation:390042715","Orphanet:600832"],"synonyms":[{"name":"Legionella infection","type":"exact"},{"name":"Legionnaires disease","type":"exact"}],"termid":"MONDO:0005823","xrefs":{"Monarch":{"xref_id":"0005823"}}}


id: PBO:0087695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the origin recognition complex (ORC); ORC directs DNA replication by binding to replication origins and is also involved in transcriptional silencing","termid":"PBO:0087695"}


id: FYPO:0000097
data:
  {"alleles_by_uniquename":{"SJAG_00266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00266","name":"atf1delta","uniquename":"SJAG_00266:allele-1"},"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_04312:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04312","name":"pka1delta","uniquename":"SJAG_04312:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118997,119052,119064,119267],"is_not":false,"summary":null,"term":"FYPO:0000097"}]},"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 caffeine. Cells stop growing (and may die) at a concentration of caffeine that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to DNA damaging agents","termid":"FYPO:0000266"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_02527":null,"SJAG_02592":null,"SJAG_04312":null},"genotype_count":4,"genotypes_by_uniquename":{"atf1delta":{"display_name":"atf1delta","display_uniquename":"atf1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00266:allele-1","expression":"Null"}]}]},"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown":{"display_name":"lig4::KanMX6(RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]},"pka1delta":{"display_name":"pka1delta","display_uniquename":"pka1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04312:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002683","FYPO:0005447","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to caffeine during vegetative growth","references_by_uniquename":{"PMID:27678009":null,"PMID:31150379":null,"PMID:37233261":null},"single_locus_annotated_genes":["SJAG_00266","SJAG_02592","SJAG_04312","SJAG_02527"],"single_locus_genotype_uniquenames":["lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","pka1delta","sty1delta","atf1delta"],"synonyms":[{"name":"hypersensitive to caffeine during vegetative growth","type":"exact"},{"name":"sensitive to caffeine during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000097","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000097":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000003":null}}


id: MONDO:0020549
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A complete hydatidiform mole or very rarely a partial mole that invades the myometrium.","definition_xrefs":["NCIT:C6985"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydatidiform mole","termid":"MONDO:0006248"},{"relation_name":"is_a","term_name":"gestational trophoblastic neoplasm","termid":"MONDO:0018944"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"invasive hydatidiform mole","secondary_identifiers":["MEDGEN:3055","Orphanet:99925","ICDO:9100/1","UMLS:C0008493","MESH:D002820","ONCOTREE:IHM","SCTID:416669000","GARD:19711"],"synonyms":[{"name":"IHM","type":"related"},{"name":"chorioadenoma","type":"exact"},{"name":"chorioadenoma Destruens","type":"exact"},{"name":"chorioadenoma destruens","type":"exact"},{"name":"invasive Mole","type":"exact"},{"name":"invasive gestational trophoblastic neoplasm","type":"exact"},{"name":"invasive hydatidiform Mole","type":"exact"},{"name":"invasive hydatidiform mole","type":"exact"}],"termid":"MONDO:0020549","xrefs":{"Monarch":{"xref_id":"0020549"}}}


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


id: FYECO:0000226
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which leucine 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":"+ leu","synonyms":[{"name":"leucine added","type":"exact"}],"termid":"FYECO:0000226"}


id: MONDO:0019357
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital cervical spinal stenosis is a rare neurological disease characterized by a congenital narrowing of the bony anatomy of the cervical spinal canal (sagittal diameter <14mm), predisposing the individual to symptomatic neural compression, such as cramps, paresthesias, pain, muscle hypertonia and weakness, myelopathy and sphincter disturbances.","definition_xrefs":["Orphanet:831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system disorder","termid":"MONDO:0002602"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital narrowing of cervical spinal canal","secondary_identifiers":["MEDGEN:1653635","GARD:18706","UMLS:C4749275"],"synonyms":[{"name":"congenital cervical spinal stenosis","type":"related"},{"name":"congenital stenosis of the cervical spine","type":"exact"}],"termid":"MONDO:0019357","xrefs":{"Monarch":{"xref_id":"0019357"}}}


id: PBO:0069228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 483, pseudogene","termid":"PBO:0069228"}


id: GO:0051716
data:
  {"annotated_genes":["SJAG_01885","SJAG_04200","SJAG_02226","SJAG_01207","SJAG_04608","SJAG_02988","SJAG_00642","SJAG_01385","SJAG_02262","SJAG_00530","SJAG_01762","SJAG_00221","SJAG_04995","SJAG_02426","SJAG_02774","SJAG_00963","SJAG_02694","SJAG_02233","SJAG_00993","SJAG_00796","SJAG_01047","SJAG_02878","SJAG_02576","SJAG_03160","SJAG_02485","SJAG_02556","SJAG_03303","SJAG_00574","SJAG_04666","SJAG_00718","SJAG_05232","SJAG_01119","SJAG_01181","SJAG_00327","SJAG_00436","SJAG_04468","SJAG_00475","SJAG_00472","SJAG_01344","SJAG_03841","SJAG_01776","SJAG_02748","SJAG_03702","SJAG_01419","SJAG_04503","SJAG_04471","SJAG_00045","SJAG_06642","SJAG_02698","SJAG_01995","SJAG_00823","SJAG_00564","SJAG_04671","SJAG_01754","SJAG_03612","SJAG_03613","SJAG_02923","SJAG_01188","SJAG_01858","SJAG_01628","SJAG_00312","SJAG_03543","SJAG_04877","SJAG_05256","SJAG_01805","SJAG_01184","SJAG_01038","SJAG_03924","SJAG_02187","SJAG_01049","SJAG_03237","SJAG_00028","SJAG_02973","SJAG_02785","SJAG_02503","SJAG_03941","SJAG_03486","SJAG_06622","SJAG_01652","SJAG_04283","SJAG_01855","SJAG_02708","SJAG_00901","SJAG_03728","SJAG_02433","SJAG_04460","SJAG_03090","SJAG_00758","SJAG_01401","SJAG_00365","SJAG_00419","SJAG_01307","SJAG_00369","SJAG_05353","SJAG_04743","SJAG_00618","SJAG_03227","SJAG_04031","SJAG_01605","SJAG_02082","SJAG_03309","SJAG_02838","SJAG_01718","SJAG_02181","SJAG_02258","SJAG_00551","SJAG_02921","SJAG_04151","SJAG_01620","SJAG_04597","SJAG_01938","SJAG_04765","SJAG_02031","SJAG_02169","SJAG_05335","SJAG_01584","SJAG_00534","SJAG_04262","SJAG_01205","SJAG_03206","SJAG_03032","SJAG_04368","SJAG_03438","SJAG_02069","SJAG_01204","SJAG_05274","SJAG_02444","SJAG_03081","SJAG_02200","SJAG_00219","SJAG_04777","SJAG_03709","SJAG_03705","SJAG_03942","SJAG_01330","SJAG_03482","SJAG_00489","SJAG_03898","SJAG_05012","SJAG_00727","SJAG_01878","SJAG_02680","SJAG_05295","SJAG_02022","SJAG_04410","SJAG_05197","SJAG_02223","SJAG_04287","SJAG_01698","SJAG_02298","SJAG_02872","SJAG_00935","SJAG_00380","SJAG_04089","SJAG_01216","SJAG_01556","SJAG_03436","SJAG_03657","SJAG_00340","SJAG_04311","SJAG_02866","SJAG_02575","SJAG_00807","SJAG_02058","SJAG_02232","SJAG_00596","SJAG_00948","SJAG_04383","SJAG_04469","SJAG_02945","SJAG_04140","SJAG_01082","SJAG_03417","SJAG_02883","SJAG_00623","SJAG_03342","SJAG_03815","SJAG_03414","SJAG_04516","SJAG_00173","SJAG_03680","SJAG_04825","SJAG_03454","SJAG_01657","SJAG_02380","SJAG_02303","SJAG_04725","SJAG_04205","SJAG_05000","SJAG_04507","SJAG_03073","SJAG_03453","SJAG_01233","SJAG_03371","SJAG_04039","SJAG_04272","SJAG_00781","SJAG_01887","SJAG_01114","SJAG_02837","SJAG_00153","SJAG_00317","SJAG_01509","SJAG_02026","SJAG_03340","SJAG_04567","SJAG_04461","SJAG_01699","SJAG_01734","SJAG_00819","SJAG_04429","SJAG_05242","SJAG_00356","SJAG_03092","SJAG_00071","SJAG_03926","SJAG_03748","SJAG_04125","SJAG_04372","SJAG_04394","SJAG_02460","SJAG_02199","SJAG_04097","SJAG_02828","SJAG_02822","SJAG_02072","SJAG_04280","SJAG_01979","SJAG_04126","SJAG_03248","SJAG_02760","SJAG_02276","SJAG_02667","SJAG_00678","SJAG_04512","SJAG_00331","SJAG_01311","SJAG_03628","SJAG_02416","SJAG_01010","SJAG_03497","SJAG_00296","SJAG_03185","SJAG_03855","SJAG_04793","SJAG_04103","SJAG_04904","SJAG_03695","SJAG_04999","SJAG_02498","SJAG_06592","SJAG_00226","SJAG_00627","SJAG_00690","SJAG_00729","SJAG_05237","SJAG_02342","SJAG_01709","SJAG_00209","SJAG_02563","SJAG_01573","SJAG_03319","SJAG_01540","SJAG_01162","SJAG_00500","SJAG_01186","SJAG_04418","SJAG_02520","SJAG_02685","SJAG_03272","SJAG_00250","SJAG_04403","SJAG_02027","SJAG_00863","SJAG_05014","SJAG_00167","SJAG_02500","SJAG_03739","SJAG_00119","SJAG_04384","SJAG_00027","SJAG_04873","SJAG_04816","SJAG_16460","SJAG_05372","SJAG_04046","SJAG_01680","SJAG_02098","SJAG_04871","SJAG_04150","SJAG_01221","SJAG_02237","SJAG_02318","SJAG_05304","SJAG_00270","SJAG_03097","SJAG_01572","SJAG_02542","SJAG_00293","SJAG_04726","SJAG_02818","SJAG_02385","SJAG_04190","SJAG_03720","SJAG_02539","SJAG_01138","SJAG_04987","SJAG_02528","SJAG_00514","SJAG_00610","SJAG_04573","SJAG_00409","SJAG_00704","SJAG_00696","SJAG_04989","SJAG_01677","SJAG_03051","SJAG_04879","SJAG_02079","SJAG_01825","SJAG_04210","SJAG_03780","SJAG_03681","SJAG_00321","SJAG_04761","SJAG_04032","SJAG_04699","SJAG_02294","SJAG_02135","SJAG_02990","SJAG_01587","SJAG_03361","SJAG_01611","SJAG_00853","SJAG_02616","SJAG_02723","SJAG_01404","SJAG_00335","SJAG_04823","SJAG_04055","SJAG_03345","SJAG_02960","SJAG_04771","SJAG_02106","SJAG_03338","SJAG_01585","SJAG_03384","SJAG_00429","SJAG_00333","SJAG_04551","SJAG_02601","SJAG_02419","SJAG_03906","SJAG_02495","SJAG_02334","SJAG_00179","SJAG_00187","SJAG_04454","SJAG_00805","SJAG_02860","SJAG_00783","SJAG_02261","SJAG_06597","SJAG_03896","SJAG_03494","SJAG_00457","SJAG_01332","SJAG_01648","SJAG_03519","SJAG_00661","SJAG_00142","SJAG_04677","SJAG_04353","SJAG_03153","SJAG_00640","SJAG_04199","SJAG_05022","SJAG_00552","SJAG_02339","SJAG_03026","SJAG_01626","SJAG_04778","SJAG_04404","SJAG_01160","SJAG_04530","SJAG_03209","SJAG_02592","SJAG_02701","SJAG_03166","SJAG_04118","SJAG_00611","SJAG_04147","SJAG_02703","SJAG_05373","SJAG_01457","SJAG_05020","SJAG_04509","SJAG_05330","SJAG_00111","SJAG_02183","SJAG_01076","SJAG_00082","SJAG_02182","SJAG_07000","SJAG_03068","SJAG_05181","SJAG_04435","SJAG_02630","SJAG_03048","SJAG_02465","SJAG_03591","SJAG_01410","SJAG_05323","SJAG_03221","SJAG_02699","SJAG_00931","SJAG_02439","SJAG_03793","SJAG_03527","SJAG_02907","SJAG_00441","SJAG_02712","SJAG_01210","SJAG_04522","SJAG_00288","SJAG_02468","SJAG_02736","SJAG_04655","SJAG_03869","SJAG_03724","SJAG_03325","SJAG_02348","SJAG_01774","SJAG_01245","SJAG_03579","SJAG_03665","SJAG_00573","SJAG_04612","SJAG_05257","SJAG_03879","SJAG_01901","SJAG_02573","SJAG_00198","SJAG_05290","SJAG_03799","SJAG_00486","SJAG_01737","SJAG_03722","SJAG_02771","SJAG_00364","SJAG_01044","SJAG_04932","SJAG_03108","SJAG_04583","SJAG_03927","SJAG_03802","SJAG_00131","SJAG_04388","SJAG_04332","SJAG_01146","SJAG_01351","SJAG_01262","SJAG_01528","SJAG_02039","SJAG_00329","SJAG_00214","SJAG_00845","SJAG_03611","SJAG_00614","SJAG_00406","SJAG_01000","SJAG_00233","SJAG_03631","SJAG_05173","SJAG_03886","SJAG_03797","SJAG_02474","SJAG_00790","SJAG_01656","SJAG_01254","SJAG_02599","SJAG_04464","SJAG_03302","SJAG_01973","SJAG_00460","SJAG_01320","SJAG_04312","SJAG_01150","SJAG_01354","SJAG_02690","SJAG_04457","SJAG_00054","SJAG_00208","SJAG_00757","SJAG_00903","SJAG_03949","SJAG_04011","SJAG_03655","SJAG_02379","SJAG_01873","SJAG_00512","SJAG_02424","SJAG_04632","SJAG_02366","SJAG_01807","SJAG_03792","SJAG_01651","SJAG_04953","SJAG_02472","SJAG_02515","SJAG_02074","SJAG_00236","SJAG_01345","SJAG_03145","SJAG_05280","SJAG_04242","SJAG_04791","SJAG_01708","SJAG_00044","SJAG_06621","SJAG_03903","SJAG_03529","SJAG_02010","SJAG_04142","SJAG_03625","SJAG_02429","SJAG_04508","SJAG_01787","SJAG_00814","SJAG_04613","SJAG_02918","SJAG_01527","SJAG_01173","SJAG_00980","SJAG_03653","SJAG_03987","SJAG_01854","SJAG_01644","SJAG_01253","SJAG_02244","SJAG_00141","SJAG_00990","SJAG_02044","SJAG_05286","SJAG_00786","SJAG_02341","SJAG_02521","SJAG_04540","SJAG_04063","SJAG_03994","SJAG_00681","SJAG_01519","SJAG_03637","SJAG_01596","SJAG_01480","SJAG_03256","SJAG_04067","SJAG_01970","SJAG_01768","SJAG_03675","SJAG_03288","SJAG_03623","SJAG_00941","SJAG_00995","SJAG_04183","SJAG_03557","SJAG_02267","SJAG_02908","SJAG_01134","SJAG_03734","SJAG_00117","SJAG_01777","SJAG_00177","SJAG_01020","SJAG_03067","SJAG_03618","SJAG_01971","SJAG_03501","SJAG_05105","SJAG_03230","SJAG_01978","SJAG_00213","SJAG_01051","SJAG_03828","SJAG_04486","SJAG_00126","SJAG_06611","SJAG_04399","SJAG_00349","SJAG_04843","SJAG_04971","SJAG_00403","SJAG_02249","SJAG_02392","SJAG_04426","SJAG_02247","SJAG_03330","SJAG_04187","SJAG_00302","SJAG_04345","SJAG_02104","SJAG_03476","SJAG_01199","SJAG_03893","SJAG_02527","SJAG_00424","SJAG_03969","SJAG_04788","SJAG_01376","SJAG_03376","SJAG_04668","SJAG_02823","SJAG_04884","SJAG_00988","SJAG_02545","SJAG_03263","SJAG_01429","SJAG_03602","SJAG_01292","SJAG_04036","SJAG_02724","SJAG_00402","SJAG_03931","SJAG_01942","SJAG_01832","SJAG_01703","SJAG_00857","SJAG_01837","SJAG_00169","SJAG_02116","SJAG_01516","SJAG_03316","SJAG_05239","SJAG_04026","SJAG_04082","SJAG_02381","SJAG_01799","SJAG_00766","SJAG_04537","SJAG_05282","SJAG_00256","SJAG_00996","SJAG_02684","SJAG_04114","SJAG_00318","SJAG_02858","SJAG_01373","SJAG_04018","SJAG_01624","SJAG_02198","SJAG_00272","SJAG_01084","SJAG_00884","SJAG_05180","SJAG_00668","SJAG_01067","SJAG_01612","SJAG_02091","SJAG_00984","SJAG_03753","SJAG_04674","SJAG_00114","SJAG_02854","SJAG_02278","SJAG_02266","SJAG_04920"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108765,93988,106603,115273,109270,105666,101601,106252,116303],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010619"},{"annotations":[118678,95631,105700,69900,115992,72935,62485,93466,92322,79703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006284"},{"annotations":[62502,76674,57350,73913],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006285"},{"annotations":[78040],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097510"},{"annotations":[74004,74913],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006287"},{"annotations":[65961],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0009785"},{"annotations":[92162,72747,97861,79318],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097720"},{"annotations":[65111,90980,97417,117124],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0019722"},{"annotations":[115883,117968,116221],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061762"},{"annotations":[110728,101895,92027],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000196"},{"annotations":[108201,105291],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007166"},{"annotations":[98963,113207,114445,118340,112034,92891,100081,94442,103372,117919,92892,87733,89876,102543,118482,98125,98774,99604,112756,87835,87738,102616,96859,92207,106360,94712,114344,113245,108471],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990748"},{"annotations":[112478],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110095"},{"annotations":[93075,70628,108186,96808,96770,117944],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098849"},{"annotations":[113484],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140114"},{"annotations":[99759,104806,108588,117110,118031,94953],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061692"},{"annotations":[104809],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140041"},{"annotations":[101972,87168],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070458"},{"annotations":[78761,104074],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070370"},{"annotations":[92165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071474"},{"annotations":[106553,65236,57533,68482,67936,63467],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098869"},{"annotations":[73363,71387,73844,75665,94438,94980,72008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034198"},{"annotations":[119095,119096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071483"},{"annotations":[88642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071276"},{"annotations":[113104,115869,109912,114422,97863,100749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071277"},{"annotations":[77385],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071244"},{"annotations":[89271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071473"},{"annotations":[75774,100196,116223,98184,69866,75780],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042149"},{"annotations":[88601,109755,100294,96236,105041,115240,115241,104757,91849,95447,90574,109754],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034605"},{"annotations":[116726,109599,100976,111458],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[77301,103538,93864,93871,100244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010106"},{"annotations":[104985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036245"},{"annotations":[92900],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071248"},{"annotations":[112035,109756,103962,70738,109757,87836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071218"},{"annotations":[101973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071500"},{"annotations":[91651,104284,95727,102544,106257,94125,114210,110092,116025,116819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071470"},{"annotations":[108689,97378,89857,73477,76693,108691,76610,93331,107555,89955,108687,90652,114211,74971,108686,88322,91922,66930,75415,101611,74815,108690,95320,63915,68004,78835,70050,108688,73128,95744,77383,108685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034599"},{"annotations":[107329,113085,71923,113084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016036"},{"annotations":[114423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035865"},{"annotations":[99931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071472"},{"annotations":[72282,94387,76973,74524,80205,71421,76210,78131],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009267"},{"annotations":[109759,102677,109758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034620"},{"annotations":[113365,107756,109389,109492,110083],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071629"},{"annotations":[94623],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045007"},{"annotations":[101330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006307"},{"annotations":[112359,118342,66189,100827,103098,112358,89754,103029,106249,69436,74483,117319,73860,70103,101071,73679,90487,112357,72346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006974"},{"annotations":[95765,71944,111471,72623,79905,88299,88920],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000729"},{"annotations":[74856,75529,64764,65409,72050],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000730"},{"annotations":[112686,72161,61474,59610,70289,73664,112684,72713,112189,87565,87890,96443,112688,118452,68354,65989,71463,112687,70874,77174,71165,97179,88656,77987,91300,77889,114391,58753,95962,71289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006281"},{"annotations":[112892,114461,94066,118304,94827,103976,88633,99436,104478,98662,106634,115340,94584,98722,96981,89810,90457,107481,73539,92136,98900,108817,92558,94366,99152,103790],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140861"},{"annotations":[74909,73998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045004"},{"annotations":[78351],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000731"},{"annotations":[76728,94994,102578,108860],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[71500,91552,78951,79160,115485,117449,71532,75726,117040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006302"},{"annotations":[88301,98817,107414,88921,116539],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990918"},{"annotations":[69725,71851,70706,77180,74128,73265,79768,99042,77966,111779,80076,74404,73068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000727"},{"annotations":[113635,116067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097680"},{"annotations":[74149,80027,77517,100369,78622,111237,117605,79186,74686,96440,103620,69948,77547,88154,115994,72231,103906,79196,102947,74054,70657,100927,96854,117462,90631,75059,94634,87805,88922,106062,76810,107501,111474,77898,105501,71113,116540,76950,79066,70418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000724"},{"annotations":[99700,111475,116541,88303,110697,88923,104792,114025],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006303"},{"annotations":[110571,76256,76767],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045002"},{"annotations":[74687],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000736"},{"annotations":[70810,117187,107898,77740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045003"},{"annotations":[115772,116519,100992,76051,98472,71008,67911,116969,113818,70441,106931,76997,113549,113951],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0030968"},{"annotations":[116616],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006984"},{"annotations":[78270,100527,104576,104492,74151,71007,107426,73100,97977,70499,107861,102678,76050,91166,70440,70413,71978,78298,116897,94478,111726,116335,87556,78517,79235,115600,107925,70818,74644,78455,89306,97595,93338,94745,78498],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036503"},{"annotations":[60939,99067,66598,103978,102629,70197],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0070987"},{"annotations":[74811,77746,73057,70195,77545,95633,103979,102630],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0042276"},{"annotations":[77924,95291],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0046294"},{"annotations":[72207,58255,63545,62179],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007186"},{"annotations":[95634],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061674"},{"annotations":[109419,79945,99200,69792],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0140469"},{"annotations":[87935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070911"},{"annotations":[115328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031142"},{"annotations":[112729,89020,87557,103160],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0180027"},{"annotations":[77741,75262,96911,104720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036297"},{"annotations":[75999,73693,76966,78910,77196,70042,87611,89685,73109,89627,91251,67775,108203,68292,71093,70936,59342,71960,76267,64890,77007,77363,78043,78846,79698,78665,110675,116062],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035556"},{"annotations":[92863,89278],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0036498"},{"annotations":[106035],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007254"},{"annotations":[103585],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1901481"},{"annotations":[103588,102553],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1901482"},{"annotations":[99730,57459],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000165"},{"annotations":[114241,106075],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905318"},{"annotations":[79053,107503,116543],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000706"},{"annotations":[78619],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044778"},{"annotations":[78326],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000707"},{"annotations":[107416,110053],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010772"},{"annotations":[115801,106372,91193],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033315"},{"annotations":[91523,107504],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000710"},{"annotations":[88819,115802,114001,106373],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051598"},{"annotations":[75074,116410],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033316"},{"annotations":[100403],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902346"},{"annotations":[73470,105701,115425,69547,115995,72334,71156,64599,72096,72374,70961,73207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006298"},{"annotations":[70336],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031930"},{"annotations":[108308,112263,70969,95899,99069,102631,102651,113645,76112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043504"},{"annotations":[79064],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097552"},{"annotations":[77389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034514"},{"annotations":[89756,94168,100295,115747,101192],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044878"},{"annotations":[77770,79792,93332,110947,114212,115748,115974],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0044773"},{"annotations":[111781,74570,115803,116845,106375,109068,70875,79199,91194,116544,93725,72017,99119,100296,98952,78625,117018],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033314"},{"annotations":[101374,115645,108643,88703,102110],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031568"},{"annotations":[109420,91071],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[94299,95607,115749,98185],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031569"},{"annotations":[89974,100297,99121,111476,116759,91195,117454,72015,75019,91557,79062,109069,88880,106376,100807],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007095"},{"annotations":[100616,74129,102111,79067,73665,88926,91196,106377,111782,115805,88881,94300,90209,78953,99122,107419,111477,95768,78624],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031573"},{"annotations":[99194,109656,101551,114244,115298,106077],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007094"},{"annotations":[72956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031990"},{"annotations":[95608,107364,99201,118057,103555,106804],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903138"},{"annotations":[99096,115358,69717,74995,94127,109422],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990625"},{"annotations":[102116],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2001033"},{"annotations":[77351,77843],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1904293"},{"annotations":[111506],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1904332"},{"annotations":[111459,91002,105658],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:2000639"},{"annotations":[89353],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036299"},{"annotations":[76242,110606],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071630"},{"annotations":[72095,76043,115997,78623,92327,67414,74132,76952,88391,69816,58602,80029,116452,76675,63782,72373,110992,65922,61925,68389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006289"},{"annotations":[109786,69899,92765,74688,93430],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1901255"},{"annotations":[74005,76727,74914,79921],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006297"},{"annotations":[108734],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006294"},{"annotations":[69977,101509,106036,94130,110093,72897],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0038066"},{"annotations":[96136,88993,96802,106037,93093,91951],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071507"},{"annotations":[70688],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000750"},{"annotations":[71538,72429,71270,92991,95687],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048015"},{"annotations":[69181,77534,66261,58090,66121,68538,60699,65342],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000160"},{"annotations":[92181,117650,89197,87845,102595,90531],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903139"},{"annotations":[116134,89022],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1900039"},{"annotations":[111783,117019],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045739"},{"annotations":[109934,93647],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2000781"},{"annotations":[107159],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2001034"},{"annotations":[101142,87612],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905287"},{"annotations":[116420,89761,102133,93569,110951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140429"},{"annotations":[78160],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2000640"},{"annotations":[87772,95770,116526,76761,88392,104181,98002,116847],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006301"},{"annotations":[79561,89525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031848"},{"annotations":[105852,98063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106300"},{"annotations":[105704],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006290"},{"annotations":[116435,116434],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000720"},{"annotations":[112220,112791,99937,105120,118527,90903],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0062200"},{"annotations":[110763,104822],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031291"},{"annotations":[100406,102949,111332,98823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036298"},{"annotations":[77307,90570,102082,75264,97256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000725"},{"annotations":[102139],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1904547"},{"annotations":[103716,103081,94982],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990611"},{"annotations":[90674,72472],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000779"},{"annotations":[109070],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010569"},{"annotations":[89957,91288,89560],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:2000815"},{"annotations":[88741,64937,99035,68420,74105,89163,58070,60844,92902],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0019430"},{"annotations":[75022,72074,69605,74828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990414"},{"annotations":[104442,118144,72634,79915,96306],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034976"},{"annotations":[103911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072429"},{"annotations":[102144],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072441"},{"annotations":[102145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990820"},{"annotations":[102146,94305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072435"},{"annotations":[105284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000749"},{"annotations":[75310,78820],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030970"},{"annotations":[75131],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007266"},{"annotations":[97874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990516"},{"annotations":[106899,100700,94177,106143,74019,89001],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031028"},{"annotations":[79838,73017,109831,117756,65390,78183,104886,59069,89689,104016,70622,73798,96085,66015,78346,90951,98287,71834,88975,108163,77036,77509,65166,73615,115081,91508,65298,105579,96147,66316,65756,70643,73004,74972],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007165"},{"annotations":[106137,111114,115331,90616],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032005"},{"annotations":[93467,76706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000012"},{"annotations":[104943],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090520"},{"annotations":[88746,89410,112311,63734,92407,93650,103727,89025,68468,64830,117975,101863,116136,118183,112562],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032933"},{"annotations":[104062,103717],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031929"},{"annotations":[92984,106417,106442,75302,98312,91853,112769,114669,79377],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0038202"},{"annotations":[76833,99141,77205,106443,108332,72382],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0038203"},{"annotations":[90634,109132,90022,69834,87936,78629,71546,90926,91740,96490,88121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006283"},{"annotations":[98064],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0019985"},{"annotations":[93315,95465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097466"},{"annotations":[68495,87773,67363,93431,103984,66228,95774,65572,69901,96882,75500,112575,60141,64624,105705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070914"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus. The process begins with detection of the stimulus by a cell and ends with a change in state or activity or the cell.","definition_xrefs":["GOC:bf","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"},{"relation_name":"is_a","term_name":"response to stimulus","termid":"GO:0050896"}],"gene_count":666,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00028":null,"SJAG_00044":null,"SJAG_00045":null,"SJAG_00054":null,"SJAG_00071":null,"SJAG_00082":null,"SJAG_00111":null,"SJAG_00114":null,"SJAG_00117":null,"SJAG_00119":null,"SJAG_00126":null,"SJAG_00131":null,"SJAG_00141":null,"SJAG_00142":null,"SJAG_00153":null,"SJAG_00167":null,"SJAG_00169":null,"SJAG_00173":null,"SJAG_00177":null,"SJAG_00179":null,"SJAG_00187":null,"SJAG_00198":null,"SJAG_00208":null,"SJAG_00209":null,"SJAG_00213":null,"SJAG_00214":null,"SJAG_00219":null,"SJAG_00221":null,"SJAG_00226":null,"SJAG_00233":null,"SJAG_00236":null,"SJAG_00250":null,"SJAG_00256":null,"SJAG_00270":null,"SJAG_00272":null,"SJAG_00288":null,"SJAG_00293":null,"SJAG_00296":null,"SJAG_00302":null,"SJAG_00312":null,"SJAG_00317":null,"SJAG_00318":null,"SJAG_00321":null,"SJAG_00327":null,"SJAG_00329":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00335":null,"SJAG_00340":null,"SJAG_00349":null,"SJAG_00356":null,"SJAG_00364":null,"SJAG_00365":null,"SJAG_00369":null,"SJAG_00380":null,"SJAG_00402":null,"SJAG_00403":null,"SJAG_00406":null,"SJAG_00409":null,"SJAG_00419":null,"SJAG_00424":null,"SJAG_00429":null,"SJAG_00436":null,"SJAG_00441":null,"SJAG_00457":null,"SJAG_00460":null,"SJAG_00472":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00489":null,"SJAG_00500":null,"SJAG_00512":null,"SJAG_00514":null,"SJAG_00530":null,"SJAG_00534":null,"SJAG_00551":null,"SJAG_00552":null,"SJAG_00564":null,"SJAG_00573":null,"SJAG_00574":null,"SJAG_00596":null,"SJAG_00610":null,"SJAG_00611":null,"SJAG_00614":null,"SJAG_00618":null,"SJAG_00623":null,"SJAG_00627":null,"SJAG_00640":null,"SJAG_00642":null,"SJAG_00661":null,"SJAG_00668":null,"SJAG_00678":null,"SJAG_00681":null,"SJAG_00690":null,"SJAG_00696":null,"SJAG_00704":null,"SJAG_00718":null,"SJAG_00727":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00758":null,"SJAG_00766":null,"SJAG_00781":null,"SJAG_00783":null,"SJAG_00786":null,"SJAG_00790":null,"SJAG_00796":null,"SJAG_00805":null,"SJAG_00807":null,"SJAG_00814":null,"SJAG_00819":null,"SJAG_00823":null,"SJAG_00845":null,"SJAG_00853":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00884":null,"SJAG_00901":null,"SJAG_00903":null,"SJAG_00931":null,"SJAG_00935":null,"SJAG_00941":null,"SJAG_00948":null,"SJAG_00963":null,"SJAG_00980":null,"SJAG_00984":null,"SJAG_00988":null,"SJAG_00990":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_00996":null,"SJAG_01000":null,"SJAG_01010":null,"SJAG_01020":null,"SJAG_01038":null,"SJAG_01044":null,"SJAG_01047":null,"SJAG_01049":null,"SJAG_01051":null,"SJAG_01067":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01114":null,"SJAG_01119":null,"SJAG_01134":null,"SJAG_01138":null,"SJAG_01146":null,"SJAG_01150":null,"SJAG_01160":null,"SJAG_01162":null,"SJAG_01173":null,"SJAG_01181":null,"SJAG_01184":null,"SJAG_01186":null,"SJAG_01188":null,"SJAG_01199":null,"SJAG_01204":null,"SJAG_01205":null,"SJAG_01207":null,"SJAG_01210":null,"SJAG_01216":null,"SJAG_01221":null,"SJAG_01233":null,"SJAG_01245":null,"SJAG_01253":null,"SJAG_01254":null,"SJAG_01262":null,"SJAG_01292":null,"SJAG_01307":null,"SJAG_01311":null,"SJAG_01320":null,"SJAG_01330":null,"SJAG_01332":null,"SJAG_01344":null,"SJAG_01345":null,"SJAG_01351":null,"SJAG_01354":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01385":null,"SJAG_01401":null,"SJAG_01404":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01429":null,"SJAG_01457":null,"SJAG_01480":null,"SJAG_01509":null,"SJAG_01516":null,"SJAG_01519":null,"SJAG_01527":null,"SJAG_01528":null,"SJAG_01540":null,"SJAG_01556":null,"SJAG_01572":null,"SJAG_01573":null,"SJAG_01584":null,"SJAG_01585":null,"SJAG_01587":null,"SJAG_01596":null,"SJAG_01605":null,"SJAG_01611":null,"SJAG_01612":null,"SJAG_01620":null,"SJAG_01624":null,"SJAG_01626":null,"SJAG_01628":null,"SJAG_01644":null,"SJAG_01648":null,"SJAG_01651":null,"SJAG_01652":null,"SJAG_01656":null,"SJAG_01657":null,"SJAG_01677":null,"SJAG_01680":null,"SJAG_01698":null,"SJAG_01699":null,"SJAG_01703":null,"SJAG_01708":null,"SJAG_01709":null,"SJAG_01718":null,"SJAG_01734":null,"SJAG_01737":null,"SJAG_01754":null,"SJAG_01762":null,"SJAG_01768":null,"SJAG_01774":null,"SJAG_01776":null,"SJAG_01777":null,"SJAG_01787":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_01807":null,"SJAG_01825":null,"SJAG_01832":null,"SJAG_01837":null,"SJAG_01854":null,"SJAG_01855":null,"SJAG_01858":null,"SJAG_01873":null,"SJAG_01878":null,"SJAG_01885":null,"SJAG_01887":null,"SJAG_01901":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01970":null,"SJAG_01971":null,"SJAG_01973":null,"SJAG_01978":null,"SJAG_01979":null,"SJAG_01995":null,"SJAG_02010":null,"SJAG_02022":null,"SJAG_02026":null,"SJAG_02027":null,"SJAG_02031":null,"SJAG_02039":null,"SJAG_02044":null,"SJAG_02058":null,"SJAG_02069":null,"SJAG_02072":null,"SJAG_02074":null,"SJAG_02079":null,"SJAG_02082":null,"SJAG_02091":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02106":null,"SJAG_02116":null,"SJAG_02135":null,"SJAG_02169":null,"SJAG_02181":null,"SJAG_02182":null,"SJAG_02183":null,"SJAG_02187":null,"SJAG_02198":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02223":null,"SJAG_02226":null,"SJAG_02232":null,"SJAG_02233":null,"SJAG_02237":null,"SJAG_02244":null,"SJAG_02247":null,"SJAG_02249":null,"SJAG_02258":null,"SJAG_02261":null,"SJAG_02262":null,"SJAG_02266":null,"SJAG_02267":null,"SJAG_02276":null,"SJAG_02278":null,"SJAG_02294":null,"SJAG_02298":null,"SJAG_02303":null,"SJAG_02318":null,"SJAG_02334":null,"SJAG_02339":null,"SJAG_02341":null,"SJAG_02342":null,"SJAG_02348":null,"SJAG_02366":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02381":null,"SJAG_02385":null,"SJAG_02392":null,"SJAG_02416":null,"SJAG_02419":null,"SJAG_02424":null,"SJAG_02426":null,"SJAG_02429":null,"SJAG_02433":null,"SJAG_02439":null,"SJAG_02444":null,"SJAG_02460":null,"SJAG_02465":null,"SJAG_02468":null,"SJAG_02472":null,"SJAG_02474":null,"SJAG_02485":null,"SJAG_02495":null,"SJAG_02498":null,"SJAG_02500":null,"SJAG_02503":null,"SJAG_02515":null,"SJAG_02520":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02528":null,"SJAG_02539":null,"SJAG_02542":null,"SJAG_02545":null,"SJAG_02556":null,"SJAG_02563":null,"SJAG_02573":null,"SJAG_02575":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02599":null,"SJAG_02601":null,"SJAG_02616":null,"SJAG_02630":null,"SJAG_02667":null,"SJAG_02680":null,"SJAG_02684":null,"SJAG_02685":null,"SJAG_02690":null,"SJAG_02694":null,"SJAG_02698":null,"SJAG_02699":null,"SJAG_02701":null,"SJAG_02703":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02723":null,"SJAG_02724":null,"SJAG_02736":null,"SJAG_02748":null,"SJAG_02760":null,"SJAG_02771":null,"SJAG_02774":null,"SJAG_02785":null,"SJAG_02818":null,"SJAG_02822":null,"SJAG_02823":null,"SJAG_02828":null,"SJAG_02837":null,"SJAG_02838":null,"SJAG_02854":null,"SJAG_02858":null,"SJAG_02860":null,"SJAG_02866":null,"SJAG_02872":null,"SJAG_02878":null,"SJAG_02883":null,"SJAG_02907":null,"SJAG_02908":null,"SJAG_02918":null,"SJAG_02921":null,"SJAG_02923":null,"SJAG_02945":null,"SJAG_02960":null,"SJAG_02973":null,"SJAG_02988":null,"SJAG_02990":null,"SJAG_03026":null,"SJAG_03032":null,"SJAG_03048":null,"SJAG_03051":null,"SJAG_03067":null,"SJAG_03068":null,"SJAG_03073":null,"SJAG_03081":null,"SJAG_03090":null,"SJAG_03092":null,"SJAG_03097":null,"SJAG_03108":null,"SJAG_03145":null,"SJAG_03153":null,"SJAG_03160":null,"SJAG_03166":null,"SJAG_03185":null,"SJAG_03206":null,"SJAG_03209":null,"SJAG_03221":null,"SJAG_03227":null,"SJAG_03230":null,"SJAG_03237":null,"SJAG_03248":null,"SJAG_03256":null,"SJAG_03263":null,"SJAG_03272":null,"SJAG_03288":null,"SJAG_03302":null,"SJAG_03303":null,"SJAG_03309":null,"SJAG_03316":null,"SJAG_03319":null,"SJAG_03325":null,"SJAG_03330":null,"SJAG_03338":null,"SJAG_03340":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03361":null,"SJAG_03371":null,"SJAG_03376":null,"SJAG_03384":null,"SJAG_03414":null,"SJAG_03417":null,"SJAG_03436":null,"SJAG_03438":null,"SJAG_03453":null,"SJAG_03454":null,"SJAG_03476":null,"SJAG_03482":null,"SJAG_03486":null,"SJAG_03494":null,"SJAG_03497":null,"SJAG_03501":null,"SJAG_03519":null,"SJAG_03527":null,"SJAG_03529":null,"SJAG_03543":null,"SJAG_03557":null,"SJAG_03579":null,"SJAG_03591":null,"SJAG_03602":null,"SJAG_03611":null,"SJAG_03612":null,"SJAG_03613":null,"SJAG_03618":null,"SJAG_03623":null,"SJAG_03625":null,"SJAG_03628":null,"SJAG_03631":null,"SJAG_03637":null,"SJAG_03653":null,"SJAG_03655":null,"SJAG_03657":null,"SJAG_03665":null,"SJAG_03675":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03702":null,"SJAG_03705":null,"SJAG_03709":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03724":null,"SJAG_03728":null,"SJAG_03734":null,"SJAG_03739":null,"SJAG_03748":null,"SJAG_03753":null,"SJAG_03780":null,"SJAG_03792":null,"SJAG_03793":null,"SJAG_03797":null,"SJAG_03799":null,"SJAG_03802":null,"SJAG_03815":null,"SJAG_03828":null,"SJAG_03841":null,"SJAG_03855":null,"SJAG_03869":null,"SJAG_03879":null,"SJAG_03886":null,"SJAG_03893":null,"SJAG_03896":null,"SJAG_03898":null,"SJAG_03903":null,"SJAG_03906":null,"SJAG_03924":null,"SJAG_03926":null,"SJAG_03927":null,"SJAG_03931":null,"SJAG_03941":null,"SJAG_03942":null,"SJAG_03949":null,"SJAG_03969":null,"SJAG_03987":null,"SJAG_03994":null,"SJAG_04011":null,"SJAG_04018":null,"SJAG_04026":null,"SJAG_04031":null,"SJAG_04032":null,"SJAG_04036":null,"SJAG_04039":null,"SJAG_04046":null,"SJAG_04055":null,"SJAG_04063":null,"SJAG_04067":null,"SJAG_04082":null,"SJAG_04089":null,"SJAG_04097":null,"SJAG_04103":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04142":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04151":null,"SJAG_04183":null,"SJAG_04187":null,"SJAG_04190":null,"SJAG_04199":null,"SJAG_04200":null,"SJAG_04205":null,"SJAG_04210":null,"SJAG_04242":null,"SJAG_04262":null,"SJAG_04272":null,"SJAG_04280":null,"SJAG_04283":null,"SJAG_04287":null,"SJAG_04311":null,"SJAG_04312":null,"SJAG_04332":null,"SJAG_04345":null,"SJAG_04353":null,"SJAG_04368":null,"SJAG_04372":null,"SJAG_04383":null,"SJAG_04384":null,"SJAG_04388":null,"SJAG_04394":null,"SJAG_04399":null,"SJAG_04403":null,"SJAG_04404":null,"SJAG_04410":null,"SJAG_04418":null,"SJAG_04426":null,"SJAG_04429":null,"SJAG_04435":null,"SJAG_04454":null,"SJAG_04457":null,"SJAG_04460":null,"SJAG_04461":null,"SJAG_04464":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04471":null,"SJAG_04486":null,"SJAG_04503":null,"SJAG_04507":null,"SJAG_04508":null,"SJAG_04509":null,"SJAG_04512":null,"SJAG_04516":null,"SJAG_04522":null,"SJAG_04530":null,"SJAG_04537":null,"SJAG_04540":null,"SJAG_04551":null,"SJAG_04567":null,"SJAG_04573":null,"SJAG_04583":null,"SJAG_04597":null,"SJAG_04608":null,"SJAG_04612":null,"SJAG_04613":null,"SJAG_04632":null,"SJAG_04655":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04671":null,"SJAG_04674":null,"SJAG_04677":null,"SJAG_04699":null,"SJAG_04725":null,"SJAG_04726":null,"SJAG_04743":null,"SJAG_04761":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04777":null,"SJAG_04778":null,"SJAG_04788":null,"SJAG_04791":null,"SJAG_04793":null,"SJAG_04816":null,"SJAG_04823":null,"SJAG_04825":null,"SJAG_04843":null,"SJAG_04871":null,"SJAG_04873":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_04884":null,"SJAG_04904":null,"SJAG_04920":null,"SJAG_04932":null,"SJAG_04953":null,"SJAG_04971":null,"SJAG_04987":null,"SJAG_04989":null,"SJAG_04995":null,"SJAG_04999":null,"SJAG_05000":null,"SJAG_05012":null,"SJAG_05014":null,"SJAG_05020":null,"SJAG_05022":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05180":null,"SJAG_05181":null,"SJAG_05197":null,"SJAG_05232":null,"SJAG_05237":null,"SJAG_05239":null,"SJAG_05242":null,"SJAG_05256":null,"SJAG_05257":null,"SJAG_05274":null,"SJAG_05280":null,"SJAG_05282":null,"SJAG_05286":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05304":null,"SJAG_05323":null,"SJAG_05330":null,"SJAG_05335":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_06592":null,"SJAG_06597":null,"SJAG_06611":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06642":null,"SJAG_07000":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to stimulus","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:23873862":null},"secondary_identifiers":["Reactome:R-HSA-8953897"],"termid":"GO:0051716","terms_by_termid":{"GO:0000012":null,"GO:0000160":null,"GO:0000165":null,"GO:0000196":null,"GO:0000706":null,"GO:0000707":null,"GO:0000710":null,"GO:0000720":null,"GO:0000724":null,"GO:0000725":null,"GO:0000727":null,"GO:0000729":null,"GO:0000730":null,"GO:0000731":null,"GO:0000736":null,"GO:0000749":null,"GO:0000750":null,"GO:0006281":null,"GO:0006283":null,"GO:0006284":null,"GO:0006285":null,"GO:0006287":null,"GO:0006289":null,"GO:0006290":null,"GO:0006294":null,"GO:0006297":null,"GO:0006298":null,"GO:0006301":null,"GO:0006302":null,"GO:0006303":null,"GO:0006307":null,"GO:0006974":null,"GO:0006984":null,"GO:0007094":null,"GO:0007095":null,"GO:0007165":null,"GO:0007166":null,"GO:0007186":null,"GO:0007254":null,"GO:0007266":null,"GO:0009267":null,"GO:0009785":null,"GO:0010106":null,"GO:0010569":null,"GO:0010619":null,"GO:0010772":null,"GO:0016036":null,"GO:0019430":null,"GO:0019722":null,"GO:0019985":null,"GO:0030968":null,"GO:0030970":null,"GO:0031028":null,"GO:0031142":null,"GO:0031291":null,"GO:0031568":null,"GO:0031569":null,"GO:0031571":null,"GO:0031573":null,"GO:0031848":null,"GO:0031929":null,"GO:0031930":null,"GO:0031990":null,"GO:0032005":null,"GO:0032933":null,"GO:0033314":null,"GO:0033315":null,"GO:0033316":null,"GO:0034198":null,"GO:0034514":null,"GO:0034599":null,"GO:0034605":null,"GO:0034620":null,"GO:0034976":null,"GO:0035556":null,"GO:0035865":null,"GO:0036245":null,"GO:0036297":null,"GO:0036298":null,"GO:0036299":null,"GO:0036498":null,"GO:0036503":null,"GO:0038066":null,"GO:0038202":null,"GO:0038203":null,"GO:0042149":null,"GO:0042276":null,"GO:0043504":null,"GO:0044773":null,"GO:0044778":null,"GO:0044878":null,"GO:0045002":null,"GO:0045003":null,"GO:0045004":null,"GO:0045007":null,"GO:0045739":null,"GO:0046294":null,"GO:0048015":null,"GO:0051598":null,"GO:0061674":null,"GO:0061692":null,"GO:0061762":null,"GO:0062200":null,"GO:0070370":null,"GO:0070458":null,"GO:0070911":null,"GO:0070914":null,"GO:0070987":null,"GO:0071218":null,"GO:0071244":null,"GO:0071248":null,"GO:0071276":null,"GO:0071277":null,"GO:0071456":null,"GO:0071470":null,"GO:0071472":null,"GO:0071473":null,"GO:0071474":null,"GO:0071483":null,"GO:0071500":null,"GO:0071507":null,"GO:0071629":null,"GO:0071630":null,"GO:0072429":null,"GO:0072435":null,"GO:0072441":null,"GO:0090520":null,"GO:0097466":null,"GO:0097510":null,"GO:0097552":null,"GO:0097680":null,"GO:0097720":null,"GO:0098849":null,"GO:0098869":null,"GO:0106300":null,"GO:0110095":null,"GO:0140041":null,"GO:0140114":null,"GO:0140429":null,"GO:0140469":null,"GO:0140861":null,"GO:0180027":null,"GO:1900039":null,"GO:1901255":null,"GO:1901481":null,"GO:1901482":null,"GO:1902346":null,"GO:1903138":null,"GO:1903139":null,"GO:1904161":null,"GO:1904293":null,"GO:1904332":null,"GO:1904547":null,"GO:1905287":null,"GO:1905318":null,"GO:1990414":null,"GO:1990516":null,"GO:1990611":null,"GO:1990625":null,"GO:1990748":null,"GO:1990820":null,"GO:1990918":null,"GO:2000639":null,"GO:2000640":null,"GO:2000779":null,"GO:2000781":null,"GO:2000815":null,"GO:2001033":null,"GO:2001034":null}}


id: PBO:0061774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OBSCN antisense RNA 1","termid":"PBO:0061774"}


id: GO:0052706
data:
  {"annotated_genes":["SJAG_00832"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103382],"is_not":false,"summary":null,"term":"GO:0052706"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-histidine + 3 S-adenosyl-L-methionine <=> 3 H(+) + hercynine + 3 S-adenosyl-L-homocysteine. This reaction is the addition of three methyl groups to L-histidine to form N-alpha,N-alpha,N-alpha-trimethyl-L-histidine (also known as hercynine).","definition_xrefs":["RHEA:38471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00832":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016741","GO:0003824"],"is_obsolete":false,"name":"L-histidine N(alpha)-methyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R01169","MetaCyc:RXN-14431","EC:2.1.1.44"],"synonyms":[{"name":"S-adenosyl-L-methionine:L-histidine Nalpha-methyltransferase activity","type":"exact"},{"name":"S-adenosyl-L-methionine:L-histidine alpha-N-methyltransferase activity","type":"exact"},{"name":"histidine N-methyltransferase activity","type":"exact"},{"name":"histidine methyltransferase activity","type":"exact"},{"name":"histidine-alpha-N-methyltransferase activity","type":"exact"}],"termid":"GO:0052706","terms_by_termid":{"GO:0052706":null}}


id: PBO:0068521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 116, pseudogene","termid":"PBO:0068521"}


id: PBO:0090855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uracil phosphoribosyltransferase Uck2","termid":"PBO:0090855"}


id: MONDO:0009486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive form of Kenny-Caffey syndrome due to mutation(s) in the TBCE gene, encoding tubulin-specific chaperone E. This condition is characterized by hypoparathyroidism with hypocalcemia, marked growth retardation, craniofacial anomalies, absent diploic space in the skull, cortical thickening of long bones with medullary stenosis, and small hands and feet.","definition_xrefs":["NCIT:C130992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Kenny-Caffey syndrome","termid":"MONDO:0016516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive Kenny-Caffey syndrome","secondary_identifiers":["OMIM:244460","MESH:C537021","MEDGEN:340923","Orphanet:93324","GARD:8367","DOID:0080722","UMLS:C1855648"],"synonyms":[{"name":"KCS1","type":"related"},{"name":"Kcs","type":"related"},{"name":"Kenny-Caffey syndrome type 1","type":"exact"},{"name":"Kenny-Caffey syndrome, autosomal recessive","type":"exact"},{"name":"Kenny-Caffey syndrome, type 1","type":"related"}],"termid":"MONDO:0009486","xrefs":{"Monarch":{"xref_id":"0009486"}}}


id: PBO:0047847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formyl peptide receptor 3","termid":"PBO:0047847"}


id: SO:0002076
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that intersects the 3' UTR of an incompletely annotated transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"incomplete_transcript_variant","termid":"SO:0002075"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"incomplete_transcript_3UTR_variant","secondary_identifiers":["http://annovar.openbioinformatics.org/en/latest/user-guide/gene/"],"synonyms":[{"name":"ANNOVAR:ncRNA_UTR3","type":"exact"},{"name":"incomplete transcript 3UTR variant","type":"related"}],"termid":"SO:0002076"}


id: PBO:0016078
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translated non-conserved orf in low complexity region","termid":"PBO:0016078"}


id: GO:0060830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Grouping of smoothened or patched receptors in a cilium, contributing to the smoothened signaling pathway.","definition_xrefs":["GOC:sdb_2009","GOC:tb","GOC:dph","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor clustering","termid":"GO:0043113"},{"relation_name":"part_of","term_name":"smoothened signaling pathway","termid":"GO:0007224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"ciliary receptor clustering involved in smoothened signaling pathway","synonyms":[{"name":"ciliary receptor clustering involved in hedgehog signaling pathway","type":"exact"},{"name":"ciliary receptor clustering involved in hh signaling pathway","type":"exact"},{"name":"ciliary receptor clustering involved in smoothened signalling pathway","type":"exact"}],"termid":"GO:0060830"}


id: MONDO:0035521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 3","termid":"MONDO:0016868"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"blepharophimosis-ptosis-epicanthus inversus syndrome plus","secondary_identifiers":["GARD:22312","UMLS:C5437588","MEDGEN:1761196","Orphanet:572333"],"synonyms":[{"name":"3q23 microdeletion syndrome","type":"exact"},{"name":"BPES plus","type":"exact"}],"termid":"MONDO:0035521","xrefs":{"Monarch":{"xref_id":"0035521"}}}


id: PBO:0079702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U-box domain containing 5","termid":"PBO:0079702"}


id: PBO:0062767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily U member 1 pseudogene","termid":"PBO:0062767"}


id: PBO:0083991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glutathione-dependent oxidoreductase; mitochondrial matrix protein involved at an early step in the biogenesis of iron-sulfur centers along with Bol1p; hydroperoxide and superoxide-radical responsive; monothiol glutaredoxin subfamily member along with Grx3p and Grx4p","termid":"PBO:0083991"}


id: GO:0001632
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with leukotriene B4, LTB4, to initiate a change in cell activity. Leukotriene B4 is also known as (6Z, 8E, 10E, 14Z)-(5S, 12R)-5,12-dihydroxyicosa-6,8,10,14-tetraen-1-oate.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukotriene receptor activity","termid":"GO:0004974"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"leukotriene B4 receptor activity","synonyms":[{"name":"BLT receptor","type":"narrow"}],"termid":"GO:0001632"}


id: PBO:0087949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translation initiation factor eIF4G and scaffold protein; subunit of the mRNA cap-binding protein complex (eIF4F) with eIF4E (Cdc33p) and eIF4A (Tif1p/Tif2p); proposed to stimulate the ATPase and helicase activities of eIF4A synergistically with eIF4G based on sequence similarity with Tif4631p; proposed to be required with eIF4E for Ded1p-mediated stimulation of mRNA recruitment during 48S preinitiation complex (PIC) assembly; associated with Pab1p-mediated poly(A)-tail stimulated, translation","termid":"PBO:0087949"}


id: PBO:0084334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kinesin-related motor protein; tracks plus-ends and stabilizes microtubules; required for mitotic spindle assembly, chromosome segregation, and 2 micron plasmid partitioning; functionally redundant with Cin8p for chromosomal but not plasmid functions","termid":"PBO:0084334"}


id: GO:0001726
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Projection at the leading edge of a crawling cell; the protrusions are supported by a microfilament meshwork.","definition_xrefs":["ISBN:0124325653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"},{"relation_name":"part_of","term_name":"cell leading edge","termid":"GO:0031252"}],"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":"ruffle","synonyms":[{"name":"membrane ruffle","type":"related"}],"termid":"GO:0001726"}


id: PBO:0050178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxy-3-methylglutaryl-CoA lyase","termid":"PBO:0050178"}


id: GO:0005517
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete calmodulin inhibitor activity (obsolete GO:0005517)","synonyms":[{"name":"calmodulin inhibitor activity","type":"exact"}],"termid":"GO:0005517"}


id: PBO:0080444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-set and immunoglobulin domain containing 1","termid":"PBO:0080444"}


id: MONDO:0002777
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pleural empyema (obsolete MONDO:0002777)","termid":"MONDO:0002777","xrefs":{"Monarch":{"xref_id":"0002777"}}}


id: PBO:0039236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-aminolevulinate synthase 1","termid":"PBO:0039236"}


id: FYPO:0001303
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of myristoyl-CoA ligase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal long-chain fatty acid-CoA ligase activity","termid":"FYPO:0001305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000654","FYPO:0005447","FYPO:0000002","FYPO:0000661","FYPO:0000652"],"is_obsolete":false,"name":"abnormal myristoyl-CoA ligase activity","synonyms":[{"name":"abnormal myristoyl-CoA synthetase activity","type":"exact"}],"termid":"FYPO:0001303"}


id: MONDO:0006408
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare adenoma of the adrenal cortex that produces androgens or estrogens.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adrenal cortex adenoma","termid":"MONDO:0003924"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sex hormone-producing adrenal cortex adenoma","secondary_identifiers":["EFO:1000523","MEDGEN:328025","NCIT:C48452","UMLS:C1710067"],"synonyms":[{"name":"Sex hormone producing adrenal cortex adenoma","type":"exact"},{"name":"Sex hormone producing adrenal cortical adenoma","type":"exact"}],"termid":"MONDO:0006408","xrefs":{"Monarch":{"xref_id":"0006408"}}}


id: GO:0030471
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The dynamics of the spindle pole body and microtubule cytoskeleton during the cell cycle. Includes spindle pole body duplication and separation and formation and elongation of the mitotic spindle. As in, but not restricted to, the fungi (Fungi, ncbi_taxonomy_id:4751).","definition_xrefs":["ISBN:0879693649"],"gene_count":0,"genotype_count":0,"name":"obsolete spindle pole body and microtubule cycle (sensu Fungi) (obsolete GO:0030471)","synonyms":[{"name":"spindle pole body and microtubule cycle (sensu Fungi)","type":"exact"},{"name":"spindle pole body and microtubule cycle (sensu Saccharomyces)","type":"narrow"}],"termid":"GO:0030471"}


id: PBO:0001057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curved DNA-binding protein Cdb4, peptidase family","termid":"PBO:0001057"}


id: MONDO:0011609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing atopic dermatitis that is associated with variation in the region 5q31-q33.","definition_xrefs":["MONDO:patterns/inherited_susceptibility","PMID:11069631","DOID:0110102"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"atopic eczema","termid":"MONDO:0004980"},{"relation_name":"is_a","term_name":"dermatitis, atopic, susceptibility to","termid":"MONDO:0100178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dermatitis, atopic, 6","secondary_identifiers":["OMIM:605845","UMLS:C1853899","MEDGEN:344154","MESH:C565279"],"synonyms":[{"name":"ATOD6","type":"exact"},{"name":"atopic dermatitis 6","type":"exact"},{"name":"atopic dermatitis type 6","type":"exact"},{"name":"dermatitis, ATOPIC, 6","type":"related"},{"name":"dermatitis, atopic, susceptibility to, 6","type":"exact"}],"termid":"MONDO:0011609","xrefs":{"Monarch":{"xref_id":"0011609"}}}


id: SO:0000853
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region that is homologous to another region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"homologous","termid":"SO:0000857"},{"relation_name":"is_a","term_name":"conserved_region","termid":"SO:0000330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homologous_region","secondary_identifiers":["http://en.wikipedia.org/wiki/Homology_(biology)"],"synonyms":[{"name":"homolog","type":"exact"},{"name":"homologous region","type":"exact"},{"name":"homologue","type":"exact"}],"termid":"SO:0000853"}


id: GO:0010186
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cellular defense response.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular defense response","termid":"GO:0010185"},{"relation_name":"is_a","term_name":"positive regulation of defense response","termid":"GO:0031349"},{"relation_name":"positively_regulates","term_name":"cellular defense response","termid":"GO:0006968"}],"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 defense response","synonyms":[{"name":"activation of cellular defense response","type":"narrow"},{"name":"positive regulation of cellular defence response","type":"exact"},{"name":"stimulation of cellular defense response","type":"narrow"},{"name":"up regulation of cellular defense response","type":"exact"},{"name":"up-regulation of cellular defense response","type":"exact"},{"name":"upregulation of cellular defense response","type":"exact"}],"termid":"GO:0010186"}


id: MONDO:0006620
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polypoid lesion that arises from the vulva and is characterized by the presence of fibrovascular stroma lined by squamous epithelium. There is no evidence of epithelial atypia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin tag","termid":"MONDO:0004026"},{"relation_name":"is_a","term_name":"polyp of vulva","termid":"MONDO:0021396"},{"relation_name":"is_a","term_name":"fibroepithelial polyp","termid":"MONDO:0060765"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vulva fibroepithelial polyp","secondary_identifiers":["DOID:8255","UMLS:C1336978","NCIT:C6857","MEDGEN:237054"],"synonyms":[{"name":"fibroepithelial polyp of the vulva","type":"exact"},{"name":"fibroepithelial polyp of vulva","type":"exact"},{"name":"mammalian vulva skin tag","type":"exact"},{"name":"skin tag of mammalian vulva","type":"exact"},{"name":"vulval fibroepithelial polyp","type":"exact"},{"name":"vulvar fibroepithelial polyp","type":"exact"},{"name":"vulvar fibroepithelial stromal polyp","type":"exact"}],"termid":"MONDO:0006620","xrefs":{"Monarch":{"xref_id":"0006620"}}}


id: GO:0102071
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 9,10-epoxy-18-hydroxystearate + H2O = 9,10,18-trihydroxystearate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 9,10-epoxy-18-hydroxystearate hydrolase activity (obsolete GO:0102071)","termid":"GO:0102071"}


id: PBO:0063122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(ADP-ribose) polymerase family member 6","termid":"PBO:0063122"}


id: PBO:0054294
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 1685","termid":"PBO:0054294"}


id: GO:0160010
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N6-(2-hydroxyisobutanoyl)-L-lysyl-[protein] = 2-hydroxy-2-methylpropanoate + L-lysyl-[protein].","definition_xrefs":["PMID:29192674"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"protein de-2-hydroxyisobutyrylase activity","secondary_identifiers":["RHEA:69176"],"termid":"GO:0160010"}


id: PBO:0090948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,2-mannosyltransferase Omh6","termid":"PBO:0090948"}


id: PBO:0036131
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_CCR4-NOT_complex_binding","termid":"PBO:0036131"}


id: GO:0042944
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of D-alanine from one side of a membrane to the other. D-alanine is the D-enantiomer of 2-aminopropanoic acid.","definition_xrefs":["GOC:jl","ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alanine transmembrane transporter activity","termid":"GO:0022858"},{"relation_name":"is_a","term_name":"D-amino acid transmembrane transporter activity","termid":"GO:0042943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"D-alanine transmembrane transporter activity","synonyms":[{"name":"D-alanine transporter activity","type":"broad"}],"termid":"GO:0042944"}


id: FYPO:0006776
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of phosphatidylinositol-4-phosphate binding by a gene product (usually a protein) in a mutant is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased phosphatidylinositol binding","termid":"FYPO:0008328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"decreased phosphatidylinositol-4-phosphate binding","synonyms":[{"name":"decreased PtdIns-4-P binding","type":"exact"},{"name":"decreased phosphatidylinositol 4-phosphate binding","type":"exact"},{"name":"reduced phosphatidylinositol-4-phosphate binding","type":"exact"}],"termid":"FYPO:0006776"}


id: PBO:0074017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 11","termid":"PBO:0074017"}


id: MONDO:0015776
data:
  {"annotated_genes":["SJAG_00702","SJAG_00326"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008972"},{"annotations":[85662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014743"}]},"cv_name":"mondo","definition":"Rhizomelic chondrodysplasia is a form chondrodysplasia punctata, a group of diseases in which the common characteristic is calcifications near joints at birth.","definition_xrefs":["Orphanet:177"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"disorder of plasmalogens biosynthesis","termid":"MONDO:0017986"},{"relation_name":"is_a","term_name":"chondrodysplasia punctata","termid":"MONDO:0019701"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525","MONDO:0005328","MONDO:0019053"],"is_obsolete":false,"name":"rhizomelic chondrodysplasia punctata","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:79471","NCIT:C85047","ICD10CM:E71.540","MESH:D018902","DOID:2580","GARD:13160","icd11.foundation:260357080","OMIMPS:215100","UMLS:C0282529","SCTID:56692003"],"synonyms":[{"name":"RCDP","type":"exact"},{"name":"chondrodysplasia punctata, rhizomelic form","type":"exact"},{"name":"rhizomelic chondrodysplasia punctata","type":"exact"},{"name":"rhizomelic chondrodysplasia punctata syndrome","type":"exact"},{"name":"rhizomelic dwarfism","type":"exact"}],"termid":"MONDO:0015776","terms_by_termid":{"MONDO:0008972":null,"MONDO:0014743":null},"xrefs":{"Monarch":{"xref_id":"0015776"}}}


id: PBO:0047573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblast growth factor binding protein 1","termid":"PBO:0047573"}


id: MONDO:0005157
data:
  {"annotated_genes":["SJAG_02527","SJAG_02460","SJAG_00980"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85953,85952],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011508"},{"annotations":[87098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009693"}]},"cv_name":"mondo","definition":"A neoplasm composed of a lymphocytic cell population which is usually malignant (clonal) by molecular genetic and/or immunophenotypic analysis. Lymphocytic neoplasms include Hodgkin and non-Hodgkin lymphomas, acute and chronic lymphocytic leukemias, and plasma cell neoplasms.","definition_xrefs":["NCIT:C7065"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematopoietic and lymphoid cell neoplasm","termid":"MONDO:0044881"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00980":null,"SJAG_02460":null,"SJAG_02527":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"lymphoid neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0598798","EFO:0001642","ICD9:200.7","ONCOTREE:LYMPH","MEDGEN:108626"],"synonyms":[{"name":"lymphocytic and plasma cell neoplasm","type":"exact"},{"name":"lymphocytic and plasma cell tumor","type":"exact"},{"name":"lymphocytic and plasma cell tumour","type":"exact"},{"name":"lymphocytic and plasmacytic neoplasm","type":"exact"},{"name":"lymphocytic neoplasm","type":"exact"},{"name":"lymphocytic tumor","type":"exact"},{"name":"lymphocytic tumour","type":"exact"},{"name":"lymphoid and plasma cell tumor","type":"exact"},{"name":"lymphoid and plasma cell tumour","type":"exact"},{"name":"lymphoid and plasmacytic neoplasm","type":"exact"},{"name":"lymphoid and plasmacytic tumor","type":"exact"},{"name":"lymphoid and plasmacytic tumour","type":"exact"},{"name":"lymphoid neoplasm","type":"exact"},{"name":"lymphoid tumor","type":"exact"},{"name":"lymphoid tumour","type":"exact"}],"termid":"MONDO:0005157","terms_by_termid":{"MONDO:0009693":null,"MONDO:0011508":null},"xrefs":{"Monarch":{"xref_id":"0005157"}}}


id: PBO:0081749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 679","termid":"PBO:0081749"}


id: PBO:0077201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TM4SF18 antisense RNA 1","termid":"PBO:0077201"}


id: PBO:0077862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomyosin 3 pseudogene 3","termid":"PBO:0077862"}


id: PBO:0063471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate dehydrogenase complex component X","termid":"PBO:0063471"}


id: PBO:0048261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactose mutarotase","termid":"PBO:0048261"}


id: PBO:0060601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-SMC condensin I complex subunit G pseudogene 1","termid":"PBO:0060601"}


id: GO:0030934
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any collagen complex which links one collagen assembly, such as a collagen fibril or sheet, to other structures.","definition_xrefs":["ISBN:0721639976"],"gene_count":0,"genotype_count":0,"name":"obsolete anchoring collagen complex (obsolete GO:0030934)","synonyms":[{"name":"connecting collagen","type":"exact"},{"name":"linking collagen","type":"exact"}],"termid":"GO:0030934"}


id: MONDO:0044256
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete skin/hair/eye pigmentation, variation in, 5 (obsolete MONDO:0044256)","secondary_identifiers":["OMIM:227240"],"synonyms":[{"name":"SHEP5","type":"related"},{"name":"skin/hair/eye pigmentation 5, Black/nonblack hair","type":"related"},{"name":"skin/hair/eye pigmentation 5, black/nonblack hair","type":"exact"},{"name":"skin/hair/eye pigmentation 5, dark/fair skin","type":"exact"},{"name":"skin/hair/eye pigmentation 5, dark/light eyes","type":"exact"},{"name":"skin/hair/eye pigmentation, variation IN, 5","type":"related"}],"termid":"MONDO:0044256","xrefs":{"Monarch":{"xref_id":"0044256"}}}


id: GO:0010649
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell communication via electrical coupling. Cell communication via electrical coupling is the process that mediates signaling interactions between one cell and another cell by transfer of current between their adjacent cytoplasms via intercellular protein channels.","definition_xrefs":["GOC:dph","GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication","termid":"GO:0010646"},{"relation_name":"regulates","term_name":"cell communication by electrical coupling","termid":"GO:0010644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell communication by electrical coupling","termid":"GO:0010649"}


id: GO:0046345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of abscisic acid, 5-(1-hydroxy-2,6,6,trimethyl-4-oxocyclohex-2-en-1-y1)-3-methylpenta-2,4-dienoic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abscisic acid metabolic process","termid":"GO:0009687"},{"relation_name":"is_a","term_name":"sesquiterpenoid catabolic process","termid":"GO:0016107"},{"relation_name":"is_a","term_name":"apocarotenoid catabolic process","termid":"GO:0043290"},{"relation_name":"is_a","term_name":"alcohol catabolic process","termid":"GO:0046164"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"},{"relation_name":"is_a","term_name":"olefinic compound catabolic process","termid":"GO:0120256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044248","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"abscisic acid catabolic process","synonyms":[{"name":"abscisic acid breakdown","type":"exact"},{"name":"abscisic acid catabolism","type":"exact"},{"name":"abscisic acid degradation","type":"exact"}],"termid":"GO:0046345"}


id: GO:0000092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle phase during which the polar microtubules elongate and the two poles of the spindle move farther apart as part of mitosis.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic anaphase","termid":"GO:0000090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0000090"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0000087"}],"interesting_parent_ids":["GO:0000087","GO:0000090","GO:0008150"],"is_obsolete":false,"name":"mitotic anaphase B","termid":"GO:0000092"}


id: GO:0016082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that converts synaptic vesicles to a state of competence for calcium triggered fusion with the active zone membrane by bringing the two membranes into very close proximity. Priming typically (but not always) occurs after docking (Jahn and Fasshauer, 2012). Primed vesicles are also capable of spontaneously fusing with the active zone membrane.","definition_xrefs":["GOC:mah","PMID:15217342","PMID:23060190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"is_a","term_name":"exocytic process","termid":"GO:0140029"},{"relation_name":"part_of","term_name":"synaptic vesicle exocytosis","termid":"GO:0016079"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0044085","GO:0023052","GO:0008150","GO:0065003","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"synaptic vesicle priming","termid":"GO:0016082"}


id: PBO:0056966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 23c","termid":"PBO:0056966"}


id: PBO:0026903
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_ribonucleotide_incorporation_on_leading_strand","termid":"PBO:0026903"}


id: PBO:0089865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinamide mononucleotide (NMN) adenylyltransferase","termid":"PBO:0089865"}


id: GO:0006677
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving glycosylceramides, any compound formed by the replacement of the glycosidic hydroxyl group of a cyclic form of a monosaccharide (or derivative) by a ceramide group.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ceramide metabolic process","termid":"GO:0006672"},{"relation_name":"is_a","term_name":"glycosphingolipid metabolic process","termid":"GO:0006687"}],"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":"glycosylceramide metabolic process","synonyms":[{"name":"glycosylceramide metabolism","type":"exact"}],"termid":"GO:0006677"}


id: PBO:0076431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 11 like 7","termid":"PBO:0076431"}


id: FYPO:0001812
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 5-phosphoribosyl diphosphate measured in a cell is greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"},{"relation_name":"is_a","term_name":"altered 5-phosphoribosyl diphosphate level","termid":"FYPO:0001811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased 5-phosphoribosyl diphosphate level","synonyms":[{"name":"increased 5-O-phosphono-alpha-D-ribofuranosyl diphosphate level","type":"exact"},{"name":"increased 5-phosphoribosyl diphosphate accumulation","type":"related"},{"name":"increased 5-phosphoribosyl diphosphate level during mitotic cell cycle","type":"related"},{"name":"increased 5-phosphoribosyl diphosphate level during vegetative growth","type":"exact"},{"name":"increased cellular 5-phosphoribosyl diphosphate level","type":"exact"}],"termid":"FYPO:0001812"}


id: PBO:0058032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4253","termid":"PBO:0058032"}


id: GO:0043884
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + corrinoid protein = CO + methylcorrinoid protein + CoA.","definition_xrefs":["EC:2.3.1.169","PMID:1748656"],"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:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"CO-methylating acetyl-CoA synthase activity","secondary_identifiers":["MetaCyc:ACETYLSYNCLTH-RXN","RHEA:45212"],"synonyms":[{"name":"ACS","type":"related"},{"name":"CO-methylating acetyl-coenzyme A synthase activity","type":"exact"},{"name":"acetyl-CoA synthase activity","type":"broad"},{"name":"acetyl-CoA:corrinoid protein O-acetyltransferase activity","type":"exact"}],"termid":"GO:0043884"}


id: GO:0090067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the size of the thalamus. The thalamus is a part of the diencephalon that is composed of the dorsal thalamus and the ventral thalamus.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure size","termid":"GO:0090066"}],"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 thalamus size","termid":"GO:0090067"}


id: MONDO:0008038
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic disease characterized by cerebellar ataxia, cytopenias and predisposition to bone marrow failure and myeloid leukemia. Neurologic features variably include slowly progressive cerebellar ataxia or balance impairment with cerebellar atrophy and periventricular white matter T2 hyperintensities in brain MRI, horizontal and vertical nystagmus, dysmetria, dysarthria, pyramidal tract signs and reduced nerve conduction velocity. Hematological abnormalities are variable and may be intermittent and include cytopenias of all cell lineages, immunodeficiency, myelodysplasia and acute myeloid leukemia.","definition_xrefs":["Orphanet:2585"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete disorder of medulla oblongata (obsolete MONDO:0015141)","termid":"MONDO:0015141"},{"relation_name":"is_a","term_name":"hereditary cerebellar ataxia","termid":"MONDO:0100310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"ataxia-pancytopenia syndrome","secondary_identifiers":["GARD:3865","MEDGEN:230896","MESH:C563233","OMIM:159550","SCTID:768556005","NCIT:C176909","UMLS:C1327919","ICD10CM:D61.0"],"synonyms":[{"name":"ATXPC","type":"related"},{"name":"ataxia-pancytopenia syndrome","type":"exact"},{"name":"myelocerebellar disorder","type":"exact"}],"termid":"MONDO:0008038","xrefs":{"Monarch":{"xref_id":"0008038"}}}


id: PBO:0090249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoplasmic phenylalanine-tRNA ligase alpha subunit Frs2","termid":"PBO:0090249"}


id: GO:0060419
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The increase in size or mass of the heart.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organ growth","termid":"GO:0035265"},{"relation_name":"part_of","term_name":"heart development","termid":"GO:0007507"}],"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":"heart growth","termid":"GO:0060419"}


id: GO:0032939
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of translation as a result of oxidative stress, a state often resulting from exposure to high levels of reactive oxygen species, e.g. superoxide anions, hydrogen peroxide (H2O2), and hydroxyl radicals.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of translation in response to stress","termid":"GO:0032056"},{"relation_name":"part_of","term_name":"cellular response to oxidative stress","termid":"GO:0034599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of translation in response to oxidative stress","synonyms":[{"name":"activation of translation in response to oxidative stress","type":"narrow"},{"name":"stimulation of translation in response to oxidative stress","type":"narrow"},{"name":"up regulation of translation in response to oxidative stress","type":"exact"},{"name":"up-regulation of translation in response to oxidative stress","type":"exact"},{"name":"upregulation of translation in response to oxidative stress","type":"exact"}],"termid":"GO:0032939"}


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


id: GO:0015188
data:
  {"annotated_genes":["SJAG_02029","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102555,109780],"is_not":false,"summary":null,"term":"GO:0015188"}]},"cv_name":"molecular_function","definition":"Enables the transfer of L-isoleucine from one side of a membrane to the other. L-isoleucine is (2R*,3R*)-2-amino-3-methylpentanoic acid.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"},{"relation_name":"is_a","term_name":"L-amino acid transmembrane transporter activity","termid":"GO:0015179"},{"relation_name":"is_a","term_name":"branched-chain amino acid transmembrane transporter activity","termid":"GO:0015658"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02029":null,"SJAG_04725":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"L-isoleucine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-isoleucine transporter activity","type":"broad"},{"name":"isoleucine/valine:sodium symporter activity","type":"narrow"},{"name":"leucine/isoleucine/valine porter activity","type":"narrow"},{"name":"leucine/valine/isoleucine permease activity","type":"narrow"}],"termid":"GO:0015188","terms_by_termid":{"GO:0015188":null}}


id: MONDO:0009036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pfeiffer-type cardiocranial syndrome is an extremely rare disorder recognized in less than ten patients worldwide and characterized by a congenital heart defect, sagittal craniosynostosis and severe developmental delay (growth retardation and intellectual deficit).","definition_xrefs":["Orphanet:2872"],"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"},{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"cardiocranial syndrome, Pfeiffer type","secondary_identifiers":["MEDGEN:346598","OMIM:218450","UMLS:C1857495","GARD:8586","MESH:C535578","SCTID:720606005","icd11.foundation:629231429"],"synonyms":[{"name":"Cardiocranial syndrome","type":"related"},{"name":"Pfeiffer Cardiocranial syndrome","type":"related"},{"name":"Pfeiffer Singer Zschiesche syndrome","type":"related"},{"name":"Pfeiffer-Singer-Zschiesche syndrome","type":"exact"},{"name":"Pfeiffer-type cardiocranial syndrome","type":"related"},{"name":"craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis","type":"related"},{"name":"craniosynostosis-congenital heart disease-intellectual disability syndrome","type":"exact"},{"name":"sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis","type":"exact"}],"termid":"MONDO:0009036","xrefs":{"Monarch":{"xref_id":"0009036"}}}


id: GO:0052557
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of the immune response of the symbiont organism; the immune response is any immune system process that functions in the calibrated response of an organism to a potential internal or invasive threat. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of symbiont immune response (obsolete GO:0052557)","synonyms":[{"name":"positive regulation by organism of symbiont immune response","type":"exact"}],"termid":"GO:0052557"}


id: PBO:0113094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-Arabinono-1,4-lactone oxidase; catalyzes the final step in biosynthesis of dehydro-D-arabinono-1,4-lactone, which is protective against oxidative stress; null mutant shows improved incorporation efficiency of noncanonical amino acids in place of amber stop codon","termid":"PBO:0113094"}


id: RO:0002591
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"has_input","termid":"RO:0002233"},{"relation_name":"is_a","term_name":"results_in_organization_of","termid":"RO:0002592"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_remodeling_of","termid":"RO:0002591"}


id: GO:0015263
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete amine/amide/polyamine channel activity (obsolete GO:0015263)","synonyms":[{"name":"amine/amide/polyamine channel activity","type":"exact"}],"termid":"GO:0015263"}


id: GO:0045696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of embryo sac egg cell differentiation.","definition_xrefs":["GOC:go_curators","GOC:mtg_plant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of embryo sac egg cell differentiation","termid":"GO:0045694"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"embryo sac egg cell differentiation","termid":"GO:0009560"}],"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 embryo sac egg cell differentiation","synonyms":[{"name":"activation of female gametophyte egg cell differentiation","type":"narrow"},{"name":"positive regulation of female gametophyte egg cell differentiation","type":"exact"},{"name":"stimulation of female gametophyte egg cell differentiation","type":"narrow"},{"name":"up regulation of female gametophyte egg cell differentiation","type":"exact"},{"name":"up-regulation of female gametophyte egg cell differentiation","type":"exact"},{"name":"upregulation of female gametophyte egg cell differentiation","type":"exact"}],"termid":"GO:0045696"}


id: PBO:0058151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4446","termid":"PBO:0058151"}


id: GO:1903603
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of thermospermine.","definition_xrefs":["GOC:TermGenie","PMID:24906355","GO_REF:0000068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine biosynthetic process","termid":"GO:0006596"},{"relation_name":"is_a","term_name":"thermospermine metabolic process","termid":"GO:1903601"}],"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":"thermospermine biosynthetic process","synonyms":[{"name":"thermospermine anabolism","type":"exact"},{"name":"thermospermine biosynthesis","type":"exact"},{"name":"thermospermine formation","type":"exact"},{"name":"thermospermine synthesis","type":"exact"}],"termid":"GO:1903603"}


id: MONDO:0001830
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by a another medical condition, by the direct effects of a substance, or by another mental disorder. The symptoms must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to factitious disorders and malingering, the physical symptoms are not under voluntary control. (apa, dsm-V)","definition_xrefs":["MESH:D013001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatoform disorder","termid":"MONDO:0003117"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"somatization disorder","secondary_identifiers":["DOID:13918","ICD10CM:F45.0","MEDGEN:99241","UMLS:C0520482","ICD9:300.81","SCTID:397923000"],"synonyms":[{"name":"Briquet's disorder","type":"exact"},{"name":"Polysomatising disorder","type":"related"},{"name":"Somatisation disorder","type":"exact"}],"termid":"MONDO:0001830","xrefs":{"Monarch":{"xref_id":"0001830"}}}


id: MONDO:0020236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Partial or complete displacement of the crystalline lens from its normal position in the eye.","definition_xrefs":["NCIT:C125484"],"gene_count":0,"genotype_count":0,"name":"obsolete lens position anomaly (obsolete MONDO:0020236)","secondary_identifiers":["HP:0001083","Orphanet:98653"],"synonyms":[{"name":"ectopia lentis","type":"exact"}],"termid":"MONDO:0020236","xrefs":{"Monarch":{"xref_id":"0020236"}}}


id: PBO:0005271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Oca2","termid":"PBO:0005271"}


id: PBO:0000582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA (m5U54) methyltransferase Trm2 (predicted)","termid":"PBO:0000582"}


id: PBO:0066397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regenerating family member 1 alpha","termid":"PBO:0066397"}


id: PBO:0004673
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperornithinemia","termid":"PBO:0004673"}


id: MONDO:0006501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete inflammatory skin disease (obsolete MONDO:0006501)","termid":"MONDO:0006501","xrefs":{"Monarch":{"xref_id":"0006501"}}}


id: PBO:0024866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smc5-6 complex SMC P-loop ATPase subunit Smc6","termid":"PBO:0024866"}


id: MONDO:0020275
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Albinism that affects the eyes, including ocular albinism and oculocutaneous albinism.","definition_xrefs":["Wikipedia:Albinism"],"gene_count":0,"genotype_count":0,"name":"obsolete oculocutaneous or ocular albinism (obsolete MONDO:0020275)","secondary_identifiers":["Orphanet:98706"],"termid":"MONDO:0020275","xrefs":{"Monarch":{"xref_id":"0020275"}}}


id: PBO:0000812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiolipin synthase/ hydrolase fusion protein (predicted)","termid":"PBO:0000812"}


id: PBO:0062743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily H member 2 pseudogene","termid":"PBO:0062743"}


id: PBO:0034248
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_syntenic_orthology_relationship_with","termid":"PBO:0034248"}


id: PBO:0048032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fascin actin-bundling protein 3","termid":"PBO:0048032"}


id: MONDO:0012344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An Alzheimer's disease that is characterized by an associated with variation in the region 9p22.1.","definition_xrefs":["DOID:0110044","PMID:18761660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset autosomal dominant Alzheimer disease","termid":"MONDO:0015140"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0000426","MONDO:0005559"],"is_obsolete":false,"name":"Alzheimer disease 11","secondary_identifiers":["UMLS:C1853360","MESH:C565228","MEDGEN:377886","OMIM:609790","GARD:16515"],"synonyms":[{"name":"AD11","type":"exact"},{"name":"Ad11","type":"related"},{"name":"Alzheimer disease 11","type":"exact"},{"name":"Alzheimer disease type 11","type":"exact"},{"name":"Alzheimer disease, familial, 11","type":"related"},{"name":"Alzheimer disease-11","type":"exact"},{"name":"Alzheimer's disease 11","type":"exact"},{"name":"Alzheimer's disease type 11","type":"exact"}],"termid":"MONDO:0012344","xrefs":{"Monarch":{"xref_id":"0012344"}}}


id: PBO:0086663
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; identified based on comparison to related yeast species; mCherry fusion protein localizes to the vacuole","termid":"PBO:0086663"}


id: PBO:0044631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"doublecortin like kinase 2","termid":"PBO:0044631"}


id: PBO:0048313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 24","termid":"PBO:0048313"}


id: PBO:0083468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene NOP58","termid":"PBO:0083468"}


id: PBO:0089195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase Stp1, unknown biological role","termid":"PBO:0089195"}


id: MONDO:0007401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Craniosynostosis, Dandy-Walker malformation and hydrocephalus is a malformation disorder characterized by sagittal craniosynostosis, Dandy-Walker malformation, hydrocephalus, craniofacial dysmorphism (including dolichocephaly, hypertelorism, micrognathia, positional ear deformity) and variable developmental delay. The inheritance pattern appears to be autosomal dominant.","definition_xrefs":["Orphanet:1538"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrocephalus","termid":"MONDO:0001150"},{"relation_name":"is_a","term_name":"familial scaphocephaly syndrome","termid":"MONDO:0015704"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0020022"],"is_obsolete":false,"name":"craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome","secondary_identifiers":["OMIM:123155","MEDGEN:325006","MESH:C563973","SCTID:720813007","UMLS:C1838347","GARD:998"],"synonyms":[{"name":"Braddock Jones Superneau syndrome","type":"related"},{"name":"Braddock-Jones-Superneau syndrome","type":"exact"},{"name":"Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus","type":"related"},{"name":"HDCPH1","type":"related"},{"name":"craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome","type":"exact"},{"name":"hydrocephalus, autosomal dominant","type":"related"},{"name":"sagittal craniosynostosis, Dandy-Walker malformation and hydrocephalus","type":"related"}],"termid":"MONDO:0007401","xrefs":{"Monarch":{"xref_id":"0007401"}}}


id: PBO:0061822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OFD1 pseudogene 12 Y-linked","termid":"PBO:0061822"}


id: PBO:0067014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 23, pseudogene","termid":"PBO:0067014"}


id: PBO:0034184
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-ends_with","termid":"PBO:0034184"}


id: PBO:0036010
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_microtubule_bundle_structure","termid":"PBO:0036010"}


id: GO:0046453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving dipyrrins (pyrromethanes), compounds containing two pyrrole rings linked through a methine, -CH=, group.","definition_xrefs":["PMID:17430001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"dipyrrin metabolic process","synonyms":[{"name":"dipyrrin metabolism","type":"exact"}],"termid":"GO:0046453"}


id: PBO:0029534
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_microcolony,_normal_volume_spheroid_cells_(obsolete_FYPO:0002188)","termid":"PBO:0029534"}


id: MONDO:0022934
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Davis Lafer syndrome","secondary_identifiers":["MEDGEN:419708","MESH:C535989","UMLS:C2931077"],"synonyms":[{"name":"Lafer Davis syndrome","type":"related"},{"name":"intellectual disability unusual facies Davis Lafer type","type":"related"},{"name":"mental retardation unusual facies Davis Lafer type","type":"related"}],"termid":"MONDO:0022934","xrefs":{"Monarch":{"xref_id":"0022934"}}}


id: PBO:0000229
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tandem fusion protein","termid":"PBO:0000229"}


id: PBO:0072635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ras suppressor protein 1 pseudogene 1","termid":"PBO:0072635"}


id: PBO:0042649
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromodomain Y like","termid":"PBO:0042649"}


id: MOD:01195
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label -","definition_xrefs":["PubMed:11813307","PubMed:15456300","PubMed:12777388","Unimod:136#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benzoyl labeling reagent light form (N-term and K)","termid":"MOD:00505"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benzoyl labeling reagent light form - site K","synonyms":[{"name":"Benzoyl","type":"related"},{"name":"labeling reagent light form (N-term & K)","type":"related"}],"termid":"MOD:01195"}


id: PBO:0060284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin light chain 1","termid":"PBO:0060284"}


id: PR:O74781
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An arginine--tRNA ligase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03348"],"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":"arginine--tRNA ligase, cytoplasmic (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC25B2.09c","secondary_identifiers":["UniProtKB:O74781"],"synonyms":[{"name":"ArgRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-RARS2","type":"exact"},{"name":"arginyl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74781"}


id: GO:0015768
data:
  {"annotated_genes":["SJAG_03960"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106081"}]},"cv_name":"biological_process","definition":"The directed movement of maltose into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Maltose is the disaccharide 4-O-alpha-D-glucopyranosyl-D-glucopyranose, an intermediate in the catabolism of glycogen and starch.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disaccharide transport","termid":"GO:0015766"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03960":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"maltose transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0015768","terms_by_termid":{"GO:0106081":null}}


id: PBO:0044819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 109B","termid":"PBO:0044819"}


id: PBO:0061309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nephrocystin 1","termid":"PBO:0061309"}


id: GO:2000326
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of ligand-dependent nuclear receptor transcription coactivator activity.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of nuclear receptor transcription coactivator activity (obsolete GO:2000326)","synonyms":[{"name":"negative regulation of ligand-dependent nuclear receptor transcription co-activator activity","type":"exact"},{"name":"negative regulation of ligand-dependent nuclear receptor transcription coactivator activity","type":"exact"}],"termid":"GO:2000326"}


id: GO:0060587
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of lipoprotein lipid oxidation. Lipoprotein lipid oxidation is the modification of a lipoprotein by oxidation of the lipid group.","definition_xrefs":["GOC:dph","GOC:tb","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lipid metabolic process","termid":"GO:0019216"},{"relation_name":"is_a","term_name":"regulation of lipoprotein oxidation","termid":"GO:0034442"},{"relation_name":"regulates","term_name":"lipoprotein lipid oxidation","termid":"GO:0034439"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of lipoprotein lipid oxidation","termid":"GO:0060587"}


id: GO:0034187
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to apolipoprotein E.","definition_xrefs":["GOC:BHF","GOC:rl"],"gene_count":0,"genotype_count":0,"name":"obsolete apolipoprotein E binding (obsolete GO:0034187)","synonyms":[{"name":"apolipoprotein E binding","type":"exact"}],"termid":"GO:0034187"}


id: GO:0034424
data:
  {"annotated_genes":["SJAG_07012","SJAG_03511"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[75024,98624],"is_not":false,"summary":null,"term":"GO:0034424"}]},"cv_name":"cellular_component","definition":"A membrane-associated protein complex that is required for a late stage of endosomal transport. In budding yeast, this complex consists of Vps55p and Vps68p proteins.","definition_xrefs":["PMID:18216282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"endosome membrane","termid":"GO:0010008"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03511":null,"SJAG_07012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0031410","GO:0005575","GO:0005768","GO:0005737"],"is_obsolete":false,"name":"Vps55/Vps68 complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0034424","terms_by_termid":{"GO:0034424":null}}


id: PR:Q9USR0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA excision repair protein ERCC-8 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR22850:SF2","PRO:DNx","OMA:SCHPO02583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA excision repair protein ckn1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC577.09","secondary_identifiers":["UniProtKB:Q9USR0"],"synonyms":[{"name":"Spom972h-ERCC8","type":"exact"}],"termid":"PR:Q9USR0"}


id: MONDO:0013779
data:
  {"annotated_genes":["SJAG_03119"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86448],"is_not":false,"summary":null,"term":"MONDO:0013779"}]},"cv_name":"mondo","definition":"Any Wiskott-Aldrich syndrome in which the cause of the disease is a mutation in the WIPF1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03119":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"Wiskott-Aldrich syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:482631","GARD:15809","NCIT:C176820","OMIM:277970","OMIM:614493","UMLS:C3281001"],"synonyms":[{"name":"WAS2","type":"related"},{"name":"WIPF1 Wiskott-Aldrich syndrome","type":"exact"},{"name":"Wipf1 deficiency","type":"related"},{"name":"Wiskott-Aldrich syndrome 2","type":"exact"},{"name":"Wiskott-Aldrich syndrome caused by mutation in WIPF1","type":"exact"},{"name":"Wiskott-Aldrich syndrome type 2","type":"exact"}],"termid":"MONDO:0013779","terms_by_termid":{"MONDO:0013779":null},"xrefs":{"Monarch":{"xref_id":"0013779"}}}


id: PATO:0001503
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A complexity quality in a bearer by virtue of the bearer's having few parts or being complicated or compound.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complexity","termid":"PATO:0001502"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"simple","termid":"PATO:0001503"}


id: PR:Q10415
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitochondrial intermediate peptidase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11804:SF5","OMA:SCHPO00249","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial intermediate peptidase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F3.10c","secondary_identifiers":["UniProtKB:Q10415"],"synonyms":[{"name":"MIP (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MIPEP","type":"exact"},{"name":"octapeptidyl aminopeptidase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10415"}


id: PBO:0080208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vestigial like family member 2","termid":"PBO:0080208"}


id: MONDO:0018944
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diverse group of pregnancy-related tumors characterized by excessive proliferation of trophoblasts. Representative examples include hydatidiform mole, gestational choriocarcinoma, and placental site trophoblastic tumor.","definition_xrefs":["NCIT:C4699"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trophoblastic neoplasm","termid":"MONDO:0002872"},{"relation_name":"is_a","term_name":"female reproductive system neoplasm","termid":"MONDO:0021148"},{"relation_name":"is_a","term_name":"pregnancy disorder","termid":"MONDO:0024575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gestational trophoblastic neoplasm","secondary_identifiers":["ICD9:630","SCTID:609519004","GARD:6498","DOID:3590","NCIT:C3110","Orphanet:59305","icd11.foundation:1972855304","UMLS:C1135868","MEDGEN:210107","MedDRA:10061988","MESH:D006828","SCTID:44782008"],"synonyms":[{"name":"GTN","type":"exact"},{"name":"GTT","type":"exact"},{"name":"gestational trophoblastic disease","type":"broad"},{"name":"gestational trophoblastic neoplasia","type":"exact"},{"name":"gestational trophoblastic tumor","type":"exact"},{"name":"gestational trophoblastic tumour","type":"exact"},{"name":"hydatidiform mole","type":"related"},{"name":"molar pregnancy","type":"related"}],"termid":"MONDO:0018944","xrefs":{"Monarch":{"xref_id":"0018944"}}}


id: PBO:0052274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 5B","termid":"PBO:0052274"}


id: PBO:0087463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of a kinetochore-microtubule binding complex; complex bridges centromeric heterochromatin and kinetochore MAPs and motors; required for sister chromatid bi-orientation and kinetochore binding of SAC components; complex also includes Spc105p; modified by sumoylation","termid":"PBO:0087463"}


id: PBO:0003816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCAAT-binding factor complex subunit Php4","termid":"PBO:0003816"}


id: PBO:0062135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily F member 2 pseudogene","termid":"PBO:0062135"}


id: PBO:0055764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lncRNA TGF-beta/SMAD3 pathway interacting","termid":"PBO:0055764"}


id: GO:0034461
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a uropod detaches from the cell substrate and retracts the rear of a migrating cell.","definition_xrefs":["GOC:mah","PMID:10704379"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uropod organization","termid":"GO:0032796"}],"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":"uropod retraction","termid":"GO:0034461"}


id: MONDO:0019552
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Centrifugal lipodystrophy is a rare, acquired, localized lipodistrophy characterized by single or, occasionally, multiple, centrifugally progressive, asymptomatic to sometimes mildly tender, hypopigmented, lipoatrophic skin depressions with weakly erymatheous inflammatory borders, typically associated with regional ipsilateral lymph nodes swelling. Lesions typically occur on lower trunk (in particular groin and abdomen region), followed by upper trunk (axilla and neighboring regions) and, rarely, neck and head. It is usually not associated with systemic disease and is typically self-resolving.","definition_xrefs":["Orphanet:90156"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localized lipodystrophy","termid":"MONDO:0019194"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"centrifugal lipodystrophy","secondary_identifiers":["MEDGEN:590539","icd11.foundation:1561732835","UMLS:C0406605","GARD:19125"],"synonyms":[{"name":"lipodystrophia centrifugalis abdominalis infantilis","type":"exact"}],"termid":"MONDO:0019552","xrefs":{"Monarch":{"xref_id":"0019552"}}}


id: GO:0052344
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 the production of phytoalexins as part of the defense response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by symbiont of host phytoalexin production (obsolete GO:0052344)","synonyms":[{"name":"activation by symbiont of host phytoalexin production","type":"narrow"},{"name":"positive regulation by organism of phytoalexin production in other organism involved in symbiotic interaction","type":"broad"},{"name":"stimulation by symbiont of host phytoalexin production","type":"narrow"},{"name":"up regulation by symbiont of host phytoalexin production","type":"exact"},{"name":"up-regulation by symbiont of host phytoalexin production","type":"exact"},{"name":"upregulation by symbiont of host phytoalexin production","type":"exact"}],"termid":"GO:0052344"}


id: PBO:0064689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 25","termid":"PBO:0064689"}


id: GO:1990690
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The joining of the lipid bilayer membrane around a Golgi medial cisterna-derived vesicle to the lipid bilayer membrane around the Golgi cis cisterna. Such vesicles include COPI-coated transport vesicles involved in retrograde transport.","definition_xrefs":["PMID:16038056","GOC:bhm","PMID:24119662"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi vesicle fusion to target membrane","termid":"GO:0048210"},{"relation_name":"is_a","term_name":"vesicle fusion with Golgi apparatus","termid":"GO:0048280"},{"relation_name":"part_of","term_name":"retrograde transport, vesicle recycling within Golgi","termid":"GO:0000301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0061024","GO:0008150"],"is_obsolete":false,"name":"Golgi medial cisterna-derived vesicle fusion with Golgi cis cisterna membrane","synonyms":[{"name":"Golgi apparatus medial cisterna-derived vesicle fusion with Golgi apparatus cis cisterna membrane","type":"exact"},{"name":"medial-Golgi cisterna-derived vesicle fusion with cis-Golgi cisterna membrane","type":"exact"}],"termid":"GO:1990690"}


id: PBO:0088697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP III complex subunit Trs85a","termid":"PBO:0088697"}


id: PBO:0041531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C16orf95 divergent transcript","termid":"PBO:0041531"}


id: PBO:0051660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"internexin neuronal intermediate filament protein alpha","termid":"PBO:0051660"}


id: PBO:0026917
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_18S_rRNA_acetylation","termid":"PBO:0026917"}


id: GO:0005072
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Activity of any of the molecules that transmit the signal from a TGF-beta receptor through the cytoplasm to the nucleus.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor, cytoplasmic mediator activity (obsolete GO:0005072)","synonyms":[{"name":"TGF-beta receptor, cytoplasmic mediator activity","type":"exact"},{"name":"TGFbeta receptor, cytoplasmic mediator activity","type":"exact"}],"termid":"GO:0005072"}


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


id: FYPO:0005595
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 a ceramide measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal cellular ceramide level","synonyms":[{"name":"normal cellular ceramide accumulation","type":"related"},{"name":"normal cellular ceramide level during mitotic cell cycle","type":"related"},{"name":"normal cellular ceramide level during vegetative growth","type":"exact"}],"termid":"FYPO:0005595"}


id: PBO:0041503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 12 open reading frame 76","termid":"PBO:0041503"}


id: PBO:0091870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alditol NADP+ 1-oxidoreductase activity","termid":"PBO:0091870"}


id: GO:0086077
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A wide pore channel activity that enables a direct cytoplasmic connection from an AV node cell to a bundle of His cell. The gap junction passes electrical signals between the cells contributing to cardiac conduction.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gap junction channel activity involved in cardiac conduction electrical coupling","termid":"GO:0086075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"gap junction channel activity involved in AV node cell-bundle of His cell electrical coupling","synonyms":[{"name":"gap junction channel activity involved in atrioventricular node cell-bundle of His cell electrical coupling","type":"exact"}],"termid":"GO:0086077"}


id: MONDO:0011071
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The disorder is characterized by thrombocytopenia of varying severity and a predisposition to hematologic malignancies. It may be caused due to germ line variations in the RUNX1, ETV6 or ANKRD26 genes.","definition_xrefs":["PMID:28600339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"inherited blood coagulation disorder","termid":"MONDO:0021181"}],"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":"hereditary thrombocytopenia and hematologic cancer predisposition syndrome","secondary_identifiers":["NCIT:C162696","MESH:C563324","SCTID:725034002","GARD:10352","Orphanet:71290"],"synonyms":[{"name":"familial platelet syndrome with predisposition to acute myelogenous leukaemia","type":"related"},{"name":"familial thrombocytopenia with propensity to acute myelogenous leukaemia","type":"related"},{"name":"hereditary thrombocytopenia and hematologic cancer predisposition syndrome","type":"exact"},{"name":"thrombocytopenia, familial, with propensity to acute myelogenous leukaemia","type":"related"}],"termid":"MONDO:0011071","xrefs":{"Monarch":{"xref_id":"0011071"}}}


id: PBO:0001115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO-targeted ubiquitin-protein ligase subunit Rfp2","termid":"PBO:0001115"}


id: MONDO:1012030
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bleeding disorder, non-human animal","termid":"MONDO:1011685"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bleeding disorder, cattle","secondary_identifiers":["OMIA:000113-9913","OMIA:000112-9913"],"synonyms":[{"name":"bleeding diathesis, cattle","type":"exact"}],"termid":"MONDO:1012030","xrefs":{"Monarch":{"xref_id":"1012030"}}}


id: PBO:0065926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rac family small GTPase 1","termid":"PBO:0065926"}


id: PBO:0001805
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.4.3.-","termid":"PBO:0001805"}


id: SO:0001418
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An experimental region, defined by a tiling array experiment to be transcribed at some level.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"experimental_feature","termid":"SO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcribed_fragment","synonyms":[{"name":"transcribed fragment","type":"exact"},{"name":"transfrag","type":"related"}],"termid":"SO:0001418"}


id: PBO:0090954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Rsd1","termid":"PBO:0090954"}


id: PBO:0049075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 101","termid":"PBO:0049075"}


id: GO:0048026
data:
  {"annotated_genes":["SJAG_02018","SJAG_01919","SJAG_03279","SJAG_02058","SJAG_01040","SJAG_00996"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73890,75137,91925,110676],"is_not":false,"summary":null,"term":"GO:0048026"},{"annotations":[89234,118154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905746"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the rate or extent of mRNA splicing via a spliceosomal mechanism.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of RNA splicing","termid":"GO:0033120"},{"relation_name":"is_a","term_name":"regulation of mRNA splicing, via spliceosome","termid":"GO:0048024"},{"relation_name":"is_a","term_name":"positive regulation of mRNA processing","termid":"GO:0050685"},{"relation_name":"positively_regulates","term_name":"mRNA splicing, via spliceosome","termid":"GO:0000398"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00996":null,"SJAG_01040":null,"SJAG_01919":null,"SJAG_02018":null,"SJAG_02058":null,"SJAG_03279":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of mRNA splicing, via spliceosome","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0035057"],"synonyms":[{"name":"activation of nuclear mRNA splicing via U2-type spliceosome","type":"narrow"},{"name":"activation of nuclear mRNA splicing, via spliceosome","type":"narrow"},{"name":"positive regulation of nuclear mRNA splicing via U2-type spliceosome","type":"narrow"},{"name":"positive regulation of nuclear mRNA splicing, via spliceosome","type":"exact"},{"name":"positive regulation of pre-mRNA splicing","type":"broad"},{"name":"stimulation of nuclear mRNA splicing via U2-type spliceosome","type":"narrow"},{"name":"stimulation of nuclear mRNA splicing, via spliceosome","type":"narrow"},{"name":"up regulation of nuclear mRNA splicing via U2-type spliceosome","type":"narrow"},{"name":"up regulation of nuclear mRNA splicing, via spliceosome","type":"exact"},{"name":"up-regulation of nuclear mRNA splicing via U2-type spliceosome","type":"narrow"},{"name":"up-regulation of nuclear mRNA splicing, via spliceosome","type":"exact"},{"name":"upregulation of nuclear mRNA splicing via U2-type spliceosome","type":"narrow"},{"name":"upregulation of nuclear mRNA splicing, via spliceosome","type":"exact"}],"termid":"GO:0048026","terms_by_termid":{"GO:0048026":null,"GO:1905746":null}}


id: GO:0007268
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The vesicular release of classical neurotransmitter molecules from a presynapse, across a chemical synapse, the subsequent activation of neurotransmitter receptors at the postsynapse of a target cell (neuron, muscle, or secretory cell) and the effects of this activation on the postsynaptic membrane potential and ionic composition of the postsynaptic cytosol. This process encompasses both spontaneous and evoked release of neurotransmitter and all parts of synaptic vesicle exocytosis. Evoked transmission starts with the arrival of an action potential at the presynapse.","definition_xrefs":["GOC:jl","MeSH:D009435"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterograde trans-synaptic signaling","termid":"GO:0098916"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"chemical synaptic transmission","secondary_identifiers":["Reactome:R-HSA-112316","Reactome:R-HSA-442729","Reactome:R-HSA-451308","Reactome:R-HSA-442720","Reactome:R-HSA-451307","Reactome:R-HSA-9619229","Wikipedia:Neurotransmission","Reactome:R-HSA-9620244","Reactome:R-HSA-9619483","Reactome:R-HSA-442742"],"synonyms":[{"name":"neurotransmission","type":"related"},{"name":"signal transmission across a synapse","type":"broad"},{"name":"synaptic transmission","type":"broad"}],"termid":"GO:0007268"}


id: GO:0097222
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The enzymatic addition of a sequence of 40-60 adenylyl residues at the 3' end of a eukaryotic mitochondrial mRNA primary transcript. Mitochondria contain both stabilizing and destabilizing poly(A) tails.","definition_xrefs":["PMID:18083837","GOC:ans"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial RNA processing","termid":"GO:0000963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0140053"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0140053"],"is_obsolete":false,"name":"mitochondrial mRNA polyadenylation","termid":"GO:0097222"}


id: GO:0008917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-glucosamine + lipopolysaccharide = UDP + N-acetyl-D-glucosaminyl-lipopolysaccharide.","definition_xrefs":["EC:2.4.1.56","GOC:mr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"lipopolysaccharide N-acetylglucosaminyltransferase activity","secondary_identifiers":["MetaCyc:RXN-22502"],"synonyms":[{"name":"LPS N-acetylglucosaminyltransferase activity","type":"exact"},{"name":"UDP-N-acetyl-D-glucosamine:lipopolysaccharide N-acetyl-D-glucosaminyltransferase activity","type":"related"},{"name":"UDP-N-acetylglucosamine-lipopolysaccharide N-acetylglucosaminyltransferase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-lipopolysaccharide acetylglucosaminyltransferase activity","type":"related"}],"termid":"GO:0008917"}


