# terms

id: MONDO:0006498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polypoid adenoma that arises from and protrudes into the lumen of the colon. Epithelial dysplasia is always present. According to the architectural pattern it is classified as tubular, tubulovillous, or villous.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon adenoma","termid":"MONDO:0000527"},{"relation_name":"is_a","term_name":"polyp of colon","termid":"MONDO:0021400"}],"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":"adenomatous colon polyp","secondary_identifiers":["UMLS:C0850572","SCTID:428054006","NCIT:C96479","EFO:1000633","HP:0005227","MEDGEN:163407"],"synonyms":[{"name":"adenomatous polyp of colon","type":"exact"},{"name":"adenomatous polyp of the colon","type":"exact"},{"name":"colon adenomatous polyp","type":"exact"},{"name":"colonic adenomatous polyp","type":"exact"}],"termid":"MONDO:0006498","xrefs":{"Monarch":{"xref_id":"0006498"}}}


id: PBO:0091627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pdc2-Repressed lncRNA","termid":"PBO:0091627"}


id: PBO:0016994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"box H/ACA small nucleolar RNA snR3","termid":"PBO:0016994"}


id: PR:Q9P3U6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ght1 gene.","definition_xrefs":["UniProtKB:Q9P3U6","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":"high-affinity glucose transporter ght1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC548.07c","synonyms":[{"name":"Spom972h-ght1","type":"exact"},{"name":"hexose transporter 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P3U6"}


id: MONDO:0006351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, usually benign myoepithelial tumor characterized by the presence of epithelioid, often vacuolated neoplastic cells. Most patients present with painless swelling in the subcutaneous or subfascial soft tissues of the extremities.","definition_xrefs":["NCIT:C6581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myoepithelial tumor","termid":"MONDO:0002380"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parachordoma","secondary_identifiers":["DOID:2647","SCTID:404086000","UMLS:C1266175","ICDO:9373/0","ICDO:9373/1","MEDGEN:266108","EFO:1000452"],"synonyms":[{"name":"parachordoma","type":"exact"}],"termid":"MONDO:0006351","xrefs":{"Monarch":{"xref_id":"0006351"}}}


id: PBO:0065137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKX antisense RNA 1","termid":"PBO:0065137"}


id: MONDO:0001510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disease of orbital part of eye adnexa","termid":"MONDO:0004751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lateral displacement of eye","secondary_identifiers":["MEDGEN:509888","UMLS:C0155272","DOID:12360","ICD9:376.36","SCTID:48747004"],"synonyms":[{"name":"lateral displacement of globe","type":"exact"}],"termid":"MONDO:0001510","xrefs":{"Monarch":{"xref_id":"0001510"}}}


id: PBO:0050643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock transcription factor Y-linked 8, pseudogene","termid":"PBO:0050643"}


id: PBO:0048046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"follistatin like 4","termid":"PBO:0048046"}


id: PBO:0063515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pancreatic and duodenal homeobox 1","termid":"PBO:0063515"}


id: PBO:0030679
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_vegetative_cell_size","termid":"PBO:0030679"}


id: GO:0019341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of dibenzo-p-dioxin, a substance composed of two benzene rings linked by two ether bonds.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dibenzo-p-dioxin metabolic process","termid":"GO:0018894"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"small molecule catabolic process","termid":"GO:0044282"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"dibenzo-p-dioxin catabolic process","secondary_identifiers":["MetaCyc:P661-PWY"],"synonyms":[{"name":"dibenzo-p-dioxin breakdown","type":"exact"},{"name":"dibenzo-p-dioxin catabolism","type":"exact"},{"name":"dibenzo-p-dioxin degradation","type":"exact"}],"termid":"GO:0019341"}


id: GO:0052023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The alteration by an organism of the levels of salicylic acid in 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 modulation by symbiont of salicylic acid levels in host (obsolete GO:0052023)","synonyms":[{"name":"modulation by organism of salicylic acid levels in other organism involved in symbiotic interaction","type":"broad"}],"termid":"GO:0052023"}


id: MONDO:0017322
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with defective bone mineralization (obsolete MONDO:0019705)","termid":"MONDO:0019705"},{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"relation_name":"is_a","term_name":"inborn vitamin metabolic disorder","termid":"MONDO:0005528"}],"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":"disorders of vitamin D metabolism","secondary_identifiers":["MEDGEN:1842308","Orphanet:289098","UMLS:C5681017","GARD:21132"],"termid":"MONDO:0017322","xrefs":{"Monarch":{"xref_id":"0017322"}}}


id: PBO:0077472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 191C","termid":"PBO:0077472"}


id: PBO:0057486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 604","termid":"PBO:0057486"}


id: PBO:0055484
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 2917","termid":"PBO:0055484"}


id: GO:0070014
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses oligo-1,6-glucosidase activity; the complex is a heterodimer located in the cell membrane, and is formed by proteolytic cleavage of a single precursor polypeptide. The two subunits have different substrate specificities.","definition_xrefs":["PMID:3366777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"},{"relation_name":"is_a","term_name":"glucosidase complex","termid":"GO:1902687"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"sucrase-isomaltase complex","secondary_identifiers":["Wikipedia:Sucrase-isomaltase"],"synonyms":[{"name":"oligo-1,6-glucosidase complex","type":"related"}],"termid":"GO:0070014"}


id: RO:0002100
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Relation between a neuron and an anatomical structure that its soma is part of.","direct_ancestors":[{"relation_name":"is_a","term_name":"overlaps","termid":"RO:0002131"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_soma_location","termid":"RO:0002100"}


id: PR:O94537
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ire1 gene.","definition_xrefs":["UniProtKB:O94537","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine-protein kinase ppk4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC167.01","synonyms":[{"name":"Spom972h-ire1","type":"exact"}],"termid":"PR:O94537"}


id: PBO:0031485
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_meiotic_spindle","termid":"PBO:0031485"}


id: PBO:0088740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exomer complex ChAPs family (Chs5p-Arf1p-binding) protein Bch1","termid":"PBO:0088740"}


id: PBO:0076917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor AP-2 epsilon","termid":"PBO:0076917"}


id: MONDO:1012023
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"distal axonopathy, non-human animal","termid":"MONDO:1011831"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal axonopathy, domestic cat","secondary_identifiers":["OMIA:000098-9685"],"termid":"MONDO:1012023","xrefs":{"Monarch":{"xref_id":"1012023"}}}


id: PBO:0033785
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_anaphase-promoting_complex-dependent_protein_catabolic_process","termid":"PBO:0033785"}


id: PR:Q9UUD9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC17G9.13c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UUD9"],"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 C17G9.13c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17G9.13c","synonyms":[{"name":"Spom972h-SPBC17G9.13c","type":"exact"}],"termid":"PR:Q9UUD9"}


id: MONDO:0005968
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The commonest and least serious of the deep mycoses, characterized by nodular lesions of the cutaneous and subcutaneous tissues. It is caused by inhalation of contaminated dust or by infection of a wound.","definition_xrefs":["MESH:D013174"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"primary systemic mycosis","termid":"MONDO:0000308"},{"relation_name":"excluded_subClassOf","term_name":"dermatomycosis","termid":"MONDO:0002040"},{"relation_name":"is_a","term_name":"fungal infectious disease","termid":"MONDO:0002041"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sporotrichosis","secondary_identifiers":["EFO:0007494","SCTID:42094007","MEDGEN:21298","GARD:7692","Orphanet:826","UMLS:C0038034","ICD10CM:B42","ICD9:117.1","DOID:14484","icd11.foundation:579570784","MedDRA:10041736"],"synonyms":[{"name":"rose gardener's disease","type":"related"}],"termid":"MONDO:0005968","xrefs":{"Monarch":{"xref_id":"0005968"}}}


id: PBO:0071307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 30","termid":"PBO:0071307"}


id: GO:1902373
data:
  {"annotated_genes":["SJAG_04946","SJAG_03283","SJAG_02573","SJAG_00797","SJAG_02370","SJAG_03883","SJAG_03696","SJAG_04825"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78602,99852,89954,78536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070935"},{"annotations":[70479,89245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048255"},{"annotations":[89545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120271"},{"annotations":[91433],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060212"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mRNA catabolic process.","definition_xrefs":["GOC:bf","PMID:22626865","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of gene expression","termid":"GO:0010628"},{"relation_name":"is_a","term_name":"regulation of mRNA catabolic process","termid":"GO:0061013"},{"relation_name":"is_a","term_name":"negative regulation of RNA catabolic process","termid":"GO:1902369"},{"relation_name":"is_a","term_name":"negative regulation of mRNA metabolic process","termid":"GO:1903312"},{"relation_name":"negatively_regulates","term_name":"mRNA catabolic process","termid":"GO:0006402"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00797":null,"SJAG_02370":null,"SJAG_02573":null,"SJAG_03283":null,"SJAG_03696":null,"SJAG_03883":null,"SJAG_04825":null,"SJAG_04946":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mRNA catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of mRNA breakdown","type":"exact"},{"name":"down regulation of mRNA catabolic process","type":"exact"},{"name":"down regulation of mRNA catabolism","type":"exact"},{"name":"down regulation of mRNA decay","type":"related"},{"name":"down regulation of mRNA degradation","type":"exact"},{"name":"down-regulation of mRNA breakdown","type":"exact"},{"name":"down-regulation of mRNA catabolic process","type":"exact"},{"name":"down-regulation of mRNA catabolism","type":"exact"},{"name":"down-regulation of mRNA decay","type":"related"},{"name":"down-regulation of mRNA degradation","type":"exact"},{"name":"downregulation of mRNA breakdown","type":"exact"},{"name":"downregulation of mRNA catabolic process","type":"exact"},{"name":"downregulation of mRNA catabolism","type":"exact"},{"name":"downregulation of mRNA decay","type":"related"},{"name":"downregulation of mRNA degradation","type":"exact"},{"name":"inhibition of mRNA breakdown","type":"narrow"},{"name":"inhibition of mRNA catabolic process","type":"narrow"},{"name":"inhibition of mRNA catabolism","type":"narrow"},{"name":"inhibition of mRNA decay","type":"related"},{"name":"inhibition of mRNA degradation","type":"narrow"},{"name":"negative regulation of mRNA breakdown","type":"exact"},{"name":"negative regulation of mRNA catabolism","type":"exact"},{"name":"negative regulation of mRNA decay","type":"related"},{"name":"negative regulation of mRNA degradation","type":"exact"}],"termid":"GO:1902373","terms_by_termid":{"GO:0048255":null,"GO:0060212":null,"GO:0070935":null,"GO:0120271":null}}


id: PBO:0065207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA processing factor 39","termid":"PBO:0065207"}


id: GO:0061978
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of mandibular joint condyle articular cartilage over time, from its formation to the mature structure.","definition_xrefs":["PMID:20679519"],"direct_ancestors":[{"relation_name":"is_a","term_name":"temporomandibular joint articular cartilage development","termid":"GO:0061976"}],"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":"mandibular condyle articular cartilage development","termid":"GO:0061978"}


id: MONDO:0023642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ocular motility disease","termid":"MONDO:0001584"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Weber syndrome","secondary_identifiers":["icd11.foundation:1609214113","ICD9:344.89","SCTID:24654003","GARD:8676","MEDGEN:96812","UMLS:C0455717"],"synonyms":[{"name":"Midbrain stroke syndromes","type":"related"},{"name":"Weber Syndrome","type":"related"},{"name":"Weber-Gubler syndrome","type":"exact"}],"termid":"MONDO:0023642","xrefs":{"Monarch":{"xref_id":"0023642"}}}


id: SO:1000115
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000115 sequence_variant_causing_complex_3D_structural_change (obsolete SO:1000115)","synonyms":[{"name":"mutation causing complex 3D structural change","type":"related"},{"name":"sequence variant causing complex 3D structural change","type":"exact"}],"termid":"SO:1000115"}


id: GO:0048810
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the analia of the female are generated and organized. The analia is the posterior-most vertral appendage that develops from the genital disc. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["GOC:mtg_sensu","PMID:11494318"],"direct_ancestors":[{"relation_name":"is_a","term_name":"analia morphogenesis","termid":"GO:0048809"},{"relation_name":"part_of","term_name":"female analia development","termid":"GO:0045497"}],"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":"female analia morphogenesis","termid":"GO:0048810"}


id: FYPO:0006213
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, and structure of the septum is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal septum morphology","synonyms":[{"name":"normal septum morphology during mitotic cell cycle","type":"related"},{"name":"normal septum morphology during vegetative growth","type":"exact"}],"termid":"FYPO:0006213"}


id: PBO:0051730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrator complex subunit 3","termid":"PBO:0051730"}


id: PBO:0005210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA ligase Lig4","termid":"PBO:0005210"}


id: GO:0048488
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A vesicle-mediated transport process, in which the synaptic vesicle membrane constituents are retrieved from the presynaptic membrane on the axon terminal after neurotransmitter secretion by exocytosis. Synaptic vesicle endocytosis can occur via clathrin-dependent and clathrin-independent mechanisms.","definition_xrefs":["GOC:mah","GOC:jid","GOC:aruk","PMID:20448150","PMID:26430111","GOC:lmg","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"presynaptic endocytosis","termid":"GO:0140238"},{"relation_name":"part_of","term_name":"synaptic vesicle recycling","termid":"GO:0036465"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"synaptic vesicle endocytosis","secondary_identifiers":["GO:0008099"],"synonyms":[{"name":"synaptic vesicle retrieval","type":"related"}],"termid":"GO:0048488"}


id: PBO:0003578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double-strand siRNA ribonuclease Eri1","termid":"PBO:0003578"}


id: GO:0062149
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events involved in the perception of pain in which a stimulus is received and converted into a molecular signal.","definition_xrefs":["PMID:19837031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of stimulus involved in sensory perception","termid":"GO:0050906"},{"relation_name":"part_of","term_name":"sensory perception of pain","termid":"GO:0019233"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of stimulus involved in sensory perception of pain","termid":"GO:0062149"}


id: MONDO:1010565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes insipidus that occurs in chicken.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"diabetes insipidus, non-human animal","termid":"MONDO:1010051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetes insipidus, chicken","secondary_identifiers":["OMIA:000278-9031"],"termid":"MONDO:1010565","xrefs":{"Monarch":{"xref_id":"1010565"}}}


id: PBO:0034137
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-directly_regulates","termid":"PBO:0034137"}


id: MONDO:0017780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"20p13 microdeletion syndrome is a rare chromosomal anomaly characterized by developmental delay, mild to moderate intellectual disability, epilepsy, and unspecific dysmorphic signs. High palate, delayed permanent tooth eruption, hypoplastic fingernails, clinodactyly and short fingers have also been reported.","definition_xrefs":["Orphanet:313781"],"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":"partial monosomy of the short arm of chromosome 20","termid":"MONDO:0016898"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20p13 microdeletion syndrome","secondary_identifiers":["MEDGEN:1655817","GARD:21360","UMLS:C4750789"],"synonyms":[{"name":"20p subtelomeric deletion syndrome","type":"exact"},{"name":"Del(20)(p13)","type":"exact"},{"name":"monosomy 20p13","type":"exact"}],"termid":"MONDO:0017780","xrefs":{"Monarch":{"xref_id":"0017780"}}}


id: PR:O94504
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trx2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94504"],"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":"thioredoxin-2, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12D12.07c","synonyms":[{"name":"Spom972h-trx2","type":"exact"},{"name":"Trx-2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94504"}


id: GO:1902360
data:
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id: GO:0010633
data:
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id: PATO:0000474
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000474 shattering value (obsolete PATO:0000474)","termid":"PATO:0000474"}


id: PBO:0040244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy related 3 pseudogene 1","termid":"PBO:0040244"}


id: PR:Q10356
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein DJ-1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02092","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":"glutathione-independent glyoxalase DJ-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22E12.03c","secondary_identifiers":["UniProtKB:Q10356"],"synonyms":[{"name":"Spom972h-PARK7","type":"exact"},{"name":"heat shock protein 31 homolog 6 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"protein DJ-1 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10356"}


id: FYPO:0002087
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id: PBO:0076856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TET2 antisense RNA 1","termid":"PBO:0076856"}


id: PBO:0081687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 608","termid":"PBO:0081687"}


id: PR:O74763
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DDB1- and CUL4-associated factor 7 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03659","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 WD repeat-containing protein C17D11.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17D11.08","secondary_identifiers":["UniProtKB:O74763"],"synonyms":[{"name":"Spom972h-DCAF7","type":"exact"}],"termid":"PR:O74763"}


id: PBO:0073422
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id: MONDO:0800175
data:
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id: GO:0170033
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id: GO:0031667
data:
  {"annotated_genes":["SJAG_04743","SJAG_00845","SJAG_04873","SJAG_04677","SJAG_01885","SJAG_04725","SJAG_00209","SJAG_02380","SJAG_01162","SJAG_00256","SJAG_00169","SJAG_03309","SJAG_03319","SJAG_00534","SJAG_03256","SJAG_04067","SJAG_00359","SJAG_03486","SJAG_02496","SJAG_04032","SJAG_04637","SJAG_00781","SJAG_04031","SJAG_02026","SJAG_03266","SJAG_02474","SJAG_03602","SJAG_02785","SJAG_01184","SJAG_00233","SJAG_00380","SJAG_02878","SJAG_02699","SJAG_04054","SJAG_02973","SJAG_03048","SJAG_01245","SJAG_02424","SJAG_03371","SJAG_00457","SJAG_04268","SJAG_01970","SJAG_03519","SJAG_01509"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71858,117477,94033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019676"},{"annotations":[71387,72008,73363,73844,94438,75665,94980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034198"},{"annotations":[75780,69866,75774,100196,116223,98184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042149"},{"annotations":[93871,103538,77301,93864,100244],"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":[107329,113085,71923,113084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016036"},{"annotations":[71421,76210,74524,76973,72282,78131,94387,80205],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009267"},{"annotations":[115328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031142"},{"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":[100970,114493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019740"},{"annotations":[101142,87612],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905287"},{"annotations":[69863],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0043609"},{"annotations":[102139],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1904547"},{"annotations":[70334,113573],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006808"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus reflecting the presence, absence, or concentration of nutrients.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stimulus","termid":"GO:0050896"}],"gene_count":44,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00209":null,"SJAG_00233":null,"SJAG_00256":null,"SJAG_00359":null,"SJAG_00380":null,"SJAG_00457":null,"SJAG_00534":null,"SJAG_00781":null,"SJAG_00845":null,"SJAG_01162":null,"SJAG_01184":null,"SJAG_01245":null,"SJAG_01509":null,"SJAG_01885":null,"SJAG_01970":null,"SJAG_02026":null,"SJAG_02380":null,"SJAG_02424":null,"SJAG_02474":null,"SJAG_02496":null,"SJAG_02699":null,"SJAG_02785":null,"SJAG_02878":null,"SJAG_02973":null,"SJAG_03048":null,"SJAG_03256":null,"SJAG_03266":null,"SJAG_03309":null,"SJAG_03319":null,"SJAG_03371":null,"SJAG_03486":null,"SJAG_03519":null,"SJAG_03602":null,"SJAG_04031":null,"SJAG_04032":null,"SJAG_04054":null,"SJAG_04067":null,"SJAG_04268":null,"SJAG_04637":null,"SJAG_04677":null,"SJAG_04725":null,"SJAG_04743":null,"SJAG_04873":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to nutrient levels","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0031667","terms_by_termid":{"GO:0006808":null,"GO:0009267":null,"GO:0010106":null,"GO:0016036":null,"GO:0019676":null,"GO:0019740":null,"GO:0031142":null,"GO:0034198":null,"GO:0036245":null,"GO:0042149":null,"GO:0043609":null,"GO:1901481":null,"GO:1901482":null,"GO:1904547":null,"GO:1905287":null}}


id: PBO:0041711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calmodulin like 3","termid":"PBO:0041711"}


id: MONDO:0018550
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder (obsolete MONDO:0018550)","secondary_identifiers":["Orphanet:431320"],"synonyms":[{"name":"SPOAN and SPOAN-related disorder","type":"exact"}],"termid":"MONDO:0018550","xrefs":{"Monarch":{"xref_id":"0018550"}}}


id: PBO:0039800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amphiregulin","termid":"PBO:0039800"}


id: MONDO:0022432
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"alves Castelo dos Santos syndrome","secondary_identifiers":["UMLS:C2931256","MESH:C536593","MEDGEN:419758"],"synonyms":[{"name":"ectodermal dysplasia syndrome of hypotrichosis, onychodysplasia, hyperkeratosis, kyphoscoliosis, and cataract","type":"related"}],"termid":"MONDO:0022432","xrefs":{"Monarch":{"xref_id":"0022432"}}}


id: PBO:0080383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar protein sorting 13 homolog B","termid":"PBO:0080383"}


id: PBO:0046198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin A3 family member B, pseudogene","termid":"PBO:0046198"}


id: PR:Q09764
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC24H6.11c gene.","definition_xrefs":["UniProtKB:Q09764","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 C24H6.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24H6.11c","synonyms":[{"name":"Spom972h-SPAC24H6.11c","type":"exact"}],"termid":"PR:Q09764"}


id: PBO:0030285
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_sulfide_level","termid":"PBO:0030285"}


id: PBO:0035978
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_trimethylation_during_vegetative_growth","termid":"PBO:0035978"}


id: PBO:0060149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation release factor 1 like","termid":"PBO:0060149"}


id: PBO:0063512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decaprenyl diphosphate synthase subunit 1 pseudogene 1","termid":"PBO:0063512"}


id: MONDO:0035511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare disorder due to poisoning characterized by acute onset of potentially life-threatening illness following ingestion, inhalation, or injection of ricin, a lectin present in the seeds of <i>Ricinus communis</i>, the castor oil plant. Clinical presentation depends on the route of administration, inhalation being the most toxic route, followed by oral ingestion. Presenting signs and symptoms include nausea, vomiting, diarrhea, hematemesis, and melena (upon ingestion), cough, wheezing, dyspnea, sore throat, and congestion (upon inhalation), and erythema, induration, blisters, capillary leak syndrome, and localized necrosis (upon injection). The condition can progress to seizures, shock, organ failure, pulmonary edema, and respiratory failure.","definition_xrefs":["Orphanet:570470"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ricin poisoning","secondary_identifiers":["GARD:22311","ICD10CM:T62.2"],"termid":"MONDO:0035511","xrefs":{"Monarch":{"xref_id":"0035511"}}}


id: FYPO:0001762
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 tRNA modification, the covalent alteration of one or more nucleotides within a tRNA molecule, is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","GO:0006400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA processing","termid":"FYPO:0001980"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal tRNA modification","synonyms":[{"name":"normal tRNA modification during mitotic cell cycle","type":"related"},{"name":"normal tRNA modification during vegetative growth","type":"exact"}],"termid":"FYPO:0001762"}


id: FYPO:0003262
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of small RNA measured in a cell is greater than normal. All types of small RNA, a particular RNA type, or a specific small RNA may be affected.","definition_xrefs":["PomBase:mah","PMID:24095277"],"gene_count":0,"genotype_count":0,"name":"obsolete increased small RNA level (obsolete FYPO:0003262)","synonyms":[{"name":"increased accumulation of small RNAs","type":"related"},{"name":"increased small RNA accumulation","type":"related"},{"name":"increased small RNA level","type":"related"},{"name":"increased small RNA level during mitotic cell cycle","type":"related"},{"name":"increased small RNA level during vegetative growth","type":"exact"},{"name":"reduced small RNA level","type":"exact"}],"termid":"FYPO:0003262"}


id: PBO:0060811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit V3","termid":"PBO:0060811"}


id: MONDO:0021126
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An characteristic of a disease that varies depending on whether the disease appears as an isolated feature or whether the disease is a syndrome consisting of multiple features.","direct_ancestors":[{"relation_name":"is_a","term_name":"disease characteristic","termid":"MONDO:0021125"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndromic or isolated","termid":"MONDO:0021126","xrefs":{"Monarch":{"xref_id":"0021126"}}}


id: PBO:0110805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription repressor Scr1, glucose sensing","termid":"PBO:0110805"}


id: GO:1900856
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of fumitremorgin B biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of fumitremorgin B biosynthetic process (obsolete GO:1900856)","synonyms":[{"name":"down regulation of fumitremorgin B biosynthetic process","type":"exact"},{"name":"down-regulation of fumitremorgin B biosynthetic process","type":"exact"},{"name":"downregulation of fumitremorgin B biosynthetic process","type":"exact"}],"termid":"GO:1900856"}


id: PBO:0039094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenosylhomocysteinase","termid":"PBO:0039094"}


id: PBO:0080995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 26","termid":"PBO:0080995"}


id: PBO:0001804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper amine oxidase Cao1","termid":"PBO:0001804"}


id: PBO:0047232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 230 member D","termid":"PBO:0047232"}


id: PBO:0028117
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_actin_cytoskeleton_morphology_during_vegetative_growth","termid":"PBO:0028117"}


id: PATO:0000550
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000550 red light sensitivity value (obsolete PATO:0000550)","termid":"PATO:0000550"}


id: PATO:0001484
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of a process which occurs near to or not long before the present.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"onset quality","termid":"PATO:0002325"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recent","termid":"PATO:0001484"}


id: PR:G2TRT2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- new22 gene.","definition_xrefs":["UniProtKB:G2TRT2","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":"UPF0612 protein new22 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCP20C8.04","synonyms":[{"name":"Spom972h-new22","type":"exact"}],"termid":"PR:G2TRT2"}


id: GO:0030142
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A vesicle that mediates transport from the Golgi to the endoplasmic reticulum.","definition_xrefs":["PMID:22160157","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport vesicle","termid":"GO:0030133"},{"relation_name":"is_a","term_name":"COPI-coated vesicle","termid":"GO:0030137"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005737","GO:0031410","GO:0005575"],"is_obsolete":false,"name":"COPI-coated Golgi to ER transport vesicle","synonyms":[{"name":"Golgi to ER constitutive secretory pathway transport vesicle","type":"exact"},{"name":"Golgi to endoplasmic reticulum transport vesicle","type":"exact"},{"name":"Golgi-ER transport vesicle","type":"exact"},{"name":"Golgi-endoplasmic reticulum transport vesicle","type":"exact"},{"name":"retrograde transport vesicle","type":"exact"}],"termid":"GO:0030142"}


id: GO:0019902
data:
  {"annotated_genes":["SJAG_04638","SJAG_03793"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72748],"is_not":false,"summary":null,"term":"GO:0019902"},{"annotations":[63361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019903"}]},"cv_name":"molecular_function","definition":"Binding to a phosphatase.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03793":null,"SJAG_04638":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"phosphatase binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"termid":"GO:0019902","terms_by_termid":{"GO:0019902":null,"GO:0019903":null}}


id: PBO:0048347
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 58","termid":"PBO:0048347"}


id: MONDO:0100419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly KIT exon 8 mutation. (A molecular genetic abnormality indicating the presence of a mutation in exon 8 of the KIT gene located within 4q11-q12.)","definition_xrefs":["NCIT:C128660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia, KIT exon 8 mutation","synonyms":[{"name":"AML, CD117 Exon 8 Mutation","type":"exact"},{"name":"AML, KIT Proto-Oncogene Tyrosine Protein Kinase Gene Exon 8 Mutation","type":"exact"},{"name":"AML, KIT exon 8 mutation","type":"exact"},{"name":"AML, c-KIT Exon 8 Mutation","type":"exact"},{"name":"AML, v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Exon 8 Mutation","type":"exact"}],"termid":"MONDO:0100419","xrefs":{"Monarch":{"xref_id":"0100419"}}}


id: MONDO:0013571
data:
  {"annotated_genes":["SJAG_04823"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85742],"is_not":false,"summary":null,"term":"MONDO:0013571"}]},"cv_name":"mondo","definition":"A congenital disorder resulting from a deficiency in erythrocyte catalase, an enzyme responsible for the breakdown of hydrogen peroxide.","definition_xrefs":["Orphanet:926"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete disorder of peroxisomal alpha-, beta- and omega-oxidation (obsolete MONDO:0017753)","termid":"MONDO:0017753"},{"relation_name":"is_a","term_name":"disorder of defective peroxisome oxidative status","termid":"MONDO:0100306"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04823":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0019053","MONDO:0005066"],"is_obsolete":false,"name":"acatalasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:75679","HGNC:1516","MESH:D020642","NANDO:1200774","OMIM:614097","DOID:2582","EFO:0004144","NCIT:C84526","SCTID:124202004","ICD9:277.6","UMLS:C0268419","GARD:363"],"synonyms":[{"name":"acatalasemia","type":"exact"},{"name":"acatalasia","type":"exact"},{"name":"catalase deficiency","type":"exact"},{"name":"deficiency of catalase","type":"exact"}],"termid":"MONDO:0013571","terms_by_termid":{"MONDO:0013571":null},"xrefs":{"Monarch":{"xref_id":"0013571"}}}


id: PBO:0090436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNase MRP subunit Rmp1/NEPRO","termid":"PBO:0090436"}


id: GO:0044503
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change in the activity of a G protein-coupled receptor in a second organism.","definition_xrefs":["GOC:fj","GOC:jl","PMID:8405712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of receptor activity in another organism","termid":"GO:0044504"}],"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":"modulation of G protein-coupled receptor activity in another organism","synonyms":[{"name":"modulation of G protein-coupled receptor activity in other organism","type":"exact"},{"name":"modulation of G-protein coupled receptor activity in other organism","type":"exact"}],"termid":"GO:0044503"}


id: PBO:0040994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bolA family member 3","termid":"PBO:0040994"}


id: MONDO:0019581
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acral persistent papular mucinosis is a rare chronic form of localized lichen myxedematosus characterized by the development of multiple symmetrical skin-colored mucinous papules exclusively on the extensor surface of the hands and distal forearms.","definition_xrefs":["Orphanet:90396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localized lichen myxedematosus","termid":"MONDO:0019446"}],"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":"acral persistent papular mucinosis","secondary_identifiers":["MEDGEN:590586","ICD9:701.8","GARD:19140","SCTID:238949006","UMLS:C0406660","icd11.foundation:712202928"],"termid":"MONDO:0019581","xrefs":{"Monarch":{"xref_id":"0019581"}}}


id: GO:0052381
data:
  {"annotated_genes":["SJAG_01575"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70694],"is_not":false,"summary":null,"term":"GO:0052381"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: dimethylallyl diphosphate + tRNA = diphosphate + tRNA containing 6-dimethylallyladenosine.","definition_xrefs":["EC:2.5.1.75"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01575":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140101"}],"interesting_parent_ids":["GO:0003674","GO:0016765","GO:0140098","GO:0003824","GO:0140101","GO:0016740"],"is_obsolete":false,"name":"tRNA dimethylallyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-6787567","RHEA:26482","GO:0004811","MetaCyc:RXN0-6274","Reactome:R-HSA-6784462"],"synonyms":[{"name":"dimethylallyl-diphosphate:tRNA dimethylallyltransferase activity","type":"exact"},{"name":"tRNA isopentenyltransferase activity","type":"related"},{"name":"tRNA prenyltransferase activity","type":"broad"}],"termid":"GO:0052381","terms_by_termid":{"GO:0052381":null}}


id: PBO:0091228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-asparaginase","termid":"PBO:0091228"}


id: GO:2000458
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of astrocyte chemotaxis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemotaxis","termid":"GO:0050920"},{"relation_name":"is_a","term_name":"regulation of glial cell migration","termid":"GO:1903975"},{"relation_name":"regulates","term_name":"astrocyte chemotaxis","termid":"GO:0035700"}],"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 astrocyte chemotaxis","termid":"GO:2000458"}


id: PBO:0012258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteiasome complex subunit beta 6","termid":"PBO:0012258"}


id: GO:0019629
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of propionate that occurs in the 2-methylcitrate cycle.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"propionate catabolic process","termid":"GO:0019543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0044248","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"propionate catabolic process, 2-methylcitrate cycle","synonyms":[{"name":"propionate breakdown, 2-methylcitrate cycle","type":"exact"},{"name":"propionate degradation, 2-methylcitrate cycle","type":"exact"}],"termid":"GO:0019629"}


id: FYPO:0008164
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 kinetochore of a chromosome is abnormal during mitotic M-phase.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to kinetochore during vegetative growth","termid":"FYPO:0001268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein localization to kinetochore during mitotic M phase","termid":"FYPO:0008164"}


id: GO:0106210
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of culmorin, a sesquiterpenoid fungal metabolite and mycotoxin produced by some ascomycete species such as Fusarium culmorum, F. graminearum, F. venenatum and Leptosphaeria oraemaris.","definition_xrefs":["PMID:19880637","GOC:ach","PMID:26673640"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpenoid biosynthetic process","termid":"GO:0016106"},{"relation_name":"is_a","term_name":"diol biosynthetic process","termid":"GO:0034312"},{"relation_name":"is_a","term_name":"mycotoxin biosynthetic process","termid":"GO:0043386"},{"relation_name":"is_a","term_name":"sesquiterpene biosynthetic process","termid":"GO:0051762"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748","GO:0006629"],"is_obsolete":false,"name":"culmorin biosynthetic process","synonyms":[{"name":"culmorin anabolism","type":"exact"},{"name":"culmorin biosynthesis","type":"exact"},{"name":"culmorin formation","type":"exact"},{"name":"culmorin synthesis","type":"exact"}],"termid":"GO:0106210"}


id: PBO:0034402
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_downstream_target_(obsolete_has_downstream_target)","termid":"PBO:0034402"}


id: PBO:0087360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spore-specific water channel; mediates the transport of water across cell membranes, developmentally controlled; may play a role in spore maturation, probably by allowing water outflow, may be involved in freeze tolerance","termid":"PBO:0087360"}


id: PR:Q9P6K4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC30C2.07 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6K4"],"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 C30C2.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC30C2.07","synonyms":[{"name":"Spom972h-SPAC30C2.07","type":"exact"}],"termid":"PR:Q9P6K4"}


id: PBO:0052785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 24","termid":"PBO:0052785"}


id: PBO:0034473
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_fatty_acid_saturation","termid":"PBO:0034473"}


id: PBO:0068062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 367","termid":"PBO:0068062"}


id: GO:0006783
data:
  {"annotated_genes":["SJAG_01786","SJAG_03862","SJAG_02876","SJAG_05283","SJAG_03173","SJAG_01841","SJAG_04397","SJAG_01155","SJAG_04944","SJAG_03961","SJAG_00097","SJAG_01372","SJAG_01192","SJAG_04109","SJAG_02896"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74046,104953,113617],"is_not":false,"summary":null,"term":"GO:0006783"},{"annotations":[78034,79709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006784"},{"annotations":[60090,63080,67264,59124,62972,79705,57224,64678],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006782"},{"annotations":[76573,71220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019354"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of heme, any compound of iron complexed in a porphyrin (tetrapyrrole) ring, from less complex precursors.","definition_xrefs":["PMID:11788607","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin-containing compound biosynthetic process","termid":"GO:0006779"},{"relation_name":"is_a","term_name":"heme metabolic process","termid":"GO:0042168"},{"relation_name":"is_a","term_name":"pigment biosynthetic process","termid":"GO:0046148"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00097":null,"SJAG_01155":null,"SJAG_01192":null,"SJAG_01372":null,"SJAG_01786":null,"SJAG_01841":null,"SJAG_02876":null,"SJAG_02896":null,"SJAG_03173":null,"SJAG_03862":null,"SJAG_03961":null,"SJAG_04109":null,"SJAG_04397":null,"SJAG_04944":null,"SJAG_05283":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"heme biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:HEMESYN2-PWY","Reactome:R-HSA-189451"],"synonyms":[{"name":"haem biosynthesis","type":"exact"},{"name":"haem biosynthetic process","type":"exact"},{"name":"heme anabolism","type":"exact"},{"name":"heme biosynthesis","type":"exact"},{"name":"heme formation","type":"exact"},{"name":"heme synthesis","type":"exact"}],"termid":"GO:0006783","terms_by_termid":{"GO:0006782":null,"GO:0006783":null,"GO:0006784":null,"GO:0019354":null}}


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


id: PBO:0028910
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_chromatin_organization_during_vegetative_growth","termid":"PBO:0028910"}


id: MONDO:0002642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm involving a trochlear nerve.","definition_xrefs":["MONDO:patterns/neoplasm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve neoplasm","termid":"MONDO:0002633"},{"relation_name":"is_a","term_name":"trochlear nerve disorder","termid":"MONDO:0007002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trochlear nerve neoplasm","secondary_identifiers":["NCIT:C5825","DOID:3421","ICD9:239.7","MEDGEN:226811","SCTID:126970001","UMLS:C1263896"],"synonyms":[{"name":"IVth cranial nerve neoplasms","type":"exact"},{"name":"IVth cranial nerve tumors","type":"exact"},{"name":"IVth cranial nerve tumours","type":"exact"},{"name":"fourth cranial nerve neoplasm","type":"exact"},{"name":"fourth cranial nerve neoplasms","type":"exact"},{"name":"fourth cranial nerve tumor","type":"exact"},{"name":"fourth cranial nerve tumors","type":"exact"},{"name":"fourth cranial nerve tumour","type":"exact"},{"name":"fourth cranial nerve tumours","type":"exact"},{"name":"neoplasm of fourth cranial nerve","type":"exact"},{"name":"neoplasm of the fourth cranial nerve","type":"exact"},{"name":"neoplasm of the trochlear nerve","type":"exact"},{"name":"neoplasm of trochlear nerve","type":"exact"},{"name":"trochlear nerve neoplasm (disease)","type":"exact"},{"name":"trochlear nerve neoplasms","type":"exact"},{"name":"trochlear nerve tumor","type":"exact"},{"name":"trochlear nerve tumors","type":"exact"},{"name":"trochlear nerve tumour","type":"exact"},{"name":"trochlear nerve tumours","type":"exact"},{"name":"tumor of fourth cranial nerve","type":"exact"},{"name":"tumor of the fourth cranial nerve","type":"exact"},{"name":"tumor of the trochlear nerve","type":"exact"},{"name":"tumor of trochlear nerve","type":"exact"},{"name":"tumour of fourth cranial nerve","type":"exact"},{"name":"tumour of the fourth cranial nerve","type":"exact"},{"name":"tumour of the trochlear nerve","type":"exact"},{"name":"tumour of trochlear nerve","type":"exact"}],"termid":"MONDO:0002642","xrefs":{"Monarch":{"xref_id":"0002642"}}}


id: PBO:0051755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interaction protein for cytohesin exchange factors 1","termid":"PBO:0051755"}


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


id: PBO:0071019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 21","termid":"PBO:0071019"}


id: GO:0008091
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Membrane associated dimeric protein (240 and 220 kDa) of erythrocytes. Forms a complex with ankyrin, actin and probably other components of the membrane cytoskeleton, so that there is a mesh of proteins underlying the plasma membrane, potentially restricting the lateral mobility of integral proteins.","definition_xrefs":["GOC:curators","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cortical actin cytoskeleton","termid":"GO:0030864"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005938"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0015629"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0015629","GO:0005938","GO:0032991"],"is_obsolete":false,"name":"spectrin","secondary_identifiers":["Wikipedia:Spectrin","NIF_Subcellular:sao536287099"],"termid":"GO:0008091"}


id: MONDO:0003691
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymoma occurring in children.","definition_xrefs":["NCIT:C8097"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant mesenchymoma","termid":"MONDO:0003633"},{"relation_name":"is_a","term_name":"childhood malignant neoplasm","termid":"MONDO:0006517"}],"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":"childhood malignant mesenchymoma","secondary_identifiers":["MEDGEN:124688","UMLS:C0279991","DOID:5893"],"synonyms":[{"name":"childhood malignant mesenchymoma","type":"exact"},{"name":"malignant mesenchymoma","type":"broad"},{"name":"malignant mesenchymoma of childhood","type":"exact"},{"name":"paediatric malignant mesenchymoma","type":"exact"},{"name":"pediatric malignant mesenchymoma","type":"exact"}],"termid":"MONDO:0003691","xrefs":{"Monarch":{"xref_id":"0003691"}}}


id: PBO:0090661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isocitrate dehydrogenase Idp1","termid":"PBO:0090661"}


id: GO:0047723
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + IMP = D-ribose 5-phosphate + hypoxanthine.","definition_xrefs":["RHEA:20469","EC:3.2.2.12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing N-glycosyl compounds","termid":"GO:0016799"}],"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:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"inosinate nucleosidase activity","secondary_identifiers":["KEGG_REACTION:R01128","MetaCyc:INOSINATE-NUCLEOSIDASE-RXN"],"synonyms":[{"name":"5'-inosinate phosphoribohydrolase activity","type":"related"}],"termid":"GO:0047723"}


id: PBO:0061306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptide FF-amide peptide precursor","termid":"PBO:0061306"}


id: GO:0032124
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the macronucleus.","definition_xrefs":["GOC:jl","PMID:10503190","GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus organization","termid":"GO:0006997"}],"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":"macronucleus organization","synonyms":[{"name":"macronuclear organization","type":"exact"},{"name":"macronuclear organization and biogenesis","type":"related"},{"name":"macronucleus organisation","type":"exact"}],"termid":"GO:0032124"}


id: MONDO:1011491
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diamond-Blackfan anemia that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Diamond-Blackfan anemia, non-human animal","termid":"MONDO:1011405"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Diamond-Blackfan anemia, dog","secondary_identifiers":["OMIA:000041-9615"],"termid":"MONDO:1011491","xrefs":{"Monarch":{"xref_id":"1011491"}}}


id: PBO:0078634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid hormone receptor interactor 4","termid":"PBO:0078634"}


id: GO:1902774
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of substances from late endosome to lysosome.","definition_xrefs":["GOC:TermGenie","GO_REF:0000076","PMID:23949442"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal transport","termid":"GO:0007041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"late endosome to lysosome transport","synonyms":[{"name":"prevacuolar compartment to lysosome transport","type":"broad"}],"termid":"GO:1902774"}


id: MONDO:0004985
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder of the brain that causes unusual shifts in mood, energy, activity levels and the ability to carry out day-to-day tasks. Often these moods range and shift from periods of elation and energized behavior to those of hopelessness and depression.","definition_xrefs":["NCIT:C34423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mood disorder","termid":"MONDO:0005371"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bipolar disorder","secondary_identifiers":["ICD10CM:F31","MEDGEN:2649","MESH:D001714","NIFSTD:birnlex_12754","ICD9:296.80","SCTID:13746004","ICD9:296.60","ICD10WHO:F31","DOID:3312","ICD9:296.89","UMLS:C0005586","ICD9:296.40"],"synonyms":[{"name":"MAFD","type":"related"},{"name":"bipolar affective disorder","type":"related"},{"name":"bipolar depression","type":"narrow"},{"name":"bipolar disorder","type":"exact"},{"name":"bipolar disorder manic phase","type":"narrow"},{"name":"depressive-manic psych.","type":"related"},{"name":"major affective disorder","type":"exact"},{"name":"major bipolar affective disorder","type":"related"},{"name":"manic bipolar I disorder","type":"narrow"},{"name":"manic bipolar affective disorder","type":"narrow"},{"name":"manic depression","type":"narrow"},{"name":"manic depressive disorder","type":"narrow"},{"name":"manic disorder","type":"narrow"},{"name":"manic-depression","type":"exact"},{"name":"manic-depressive illness","type":"related"},{"name":"manic-depressive psychosis","type":"related"},{"name":"mixed bipolar disorder","type":"narrow"}],"termid":"MONDO:0004985","xrefs":{"Monarch":{"xref_id":"0004985"}}}


id: FYPO:0007389
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 spindle pole body (SPB)-led chromosome movement in mitotic interphase takes place at an abnormal angle relative to the long axis of the cell. Normally, the SPB oscillation angle remains nearly parallel to the long axis.","definition_xrefs":["PMID:18495844","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body-led chromosome movement during mitotic interphase","termid":"FYPO:0005348"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal angle of spindle pole body-led chromosome movement during mitotic interphase","synonyms":[{"name":"abnormal angle of SPB-led chromosome movement during mitotic interphase","type":"exact"},{"name":"abnormal angle of mitotic SPB oscillation during mitotic interphase","type":"exact"},{"name":"abnormal angle of mitotic spindle pole body movement during mitotic interphase","type":"exact"},{"name":"abnormal angle of mitotic spindle pole body oscillation during mitotic interphase","type":"exact"},{"name":"abnormal angle of spindle pole body-led chromosome movement during interphase of mitotic cell cycle","type":"exact"},{"name":"abnormal angle of spindle pole body-led chromosome movement during mitotic interphase during vegetative growth","type":"exact"},{"name":"increased angle of spindle pole body-led chromosome movement during mitotic interphase","type":"narrow"},{"name":"increased trajectory angle of SPB oscillation","type":"related"},{"name":"spindle pole body-led chromosome movement during mitotic interphase at abnormal angle","type":"exact"}],"termid":"FYPO:0007389"}


id: MONDO:0012028
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autoimmune disease","termid":"MONDO:0007179"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune disease, susceptibility to, 3","secondary_identifiers":["OMIM:608392","MEDGEN:333993","UMLS:C1842112"],"synonyms":[{"name":"AIS3","type":"exact"},{"name":"autoimmune disease susceptibility locus, chromosome 8-related","type":"related"},{"name":"autoimmune disease, susceptibility to, 3","type":"exact"},{"name":"vitiligo-associated multiple autoimmune disease susceptibility 4","type":"related"}],"termid":"MONDO:0012028","xrefs":{"Monarch":{"xref_id":"0012028"}}}


id: GO:1990440
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of an endoplasmic reticulum stress.","definition_xrefs":["GOC:PARL","GOC:bf","PMID:21113145"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress (obsolete GO:1990440)","synonyms":[{"name":"ER stress-induced upregulation of transcription","type":"broad"},{"name":"activation of transcription from RNA polymerase II promoter in response to ER stress","type":"exact"},{"name":"stimulation of transcription from RNA polymerase II promoter in response to ER stress","type":"exact"},{"name":"up-regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress","type":"exact"},{"name":"up-regulation of transcription induced by ER stress","type":"broad"},{"name":"upregulation of Pol II transcription induced by ER stress","type":"exact"},{"name":"upregulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress","type":"exact"}],"termid":"GO:1990440"}


id: PBO:0045908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EF-hand calcium binding domain 6","termid":"PBO:0045908"}


id: PBO:0069929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1222, pseudogene","termid":"PBO:0069929"}


id: PBO:0086584
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; emerging ORF that arose de novo from non-genic locus; identified by gene-trapping, microarray-based expression analysis, and genome-wide homology searching; localizes to mitochondria","termid":"PBO:0086584"}


id: MONDO:0011891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A childhood absence epilepsy that is characterized by mutations in the GABRG2 gene, which cause a spectrum of seizure disorders, ranging from early-onset isolated febrile seizures (FS) to childhood absence epilepsy (CAE) to generalized epilepsy with febrile seizures plus, type 3 (GEFS+3), which tends to represent a more severe phenotype.","definition_xrefs":["OMIM:607681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"febrile seizures, familial","termid":"MONDO:0000032"},{"relation_name":"is_a","term_name":"childhood absence epilepsy","termid":"MONDO:0010826"},{"relation_name":"is_a","term_name":"generalized epilepsy with febrile seizures plus","termid":"MONDO:0018214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"febrile seizures, familial, 8","secondary_identifiers":["GARD:18058","MEDGEN:370755","OMIM:611277","DOID:0111298","MESH:C565811","UMLS:C1969810"],"synonyms":[{"name":"ECA2","type":"related"},{"name":"GABRG2 childhood absence epilepsy","type":"exact"},{"name":"GABRG2 generalised epilepsy with febrile seizures plus","type":"exact"},{"name":"GABRG2 generalized epilepsy with febrile seizures plus","type":"exact"},{"name":"GEFSP3","type":"related"},{"name":"Gefs+, type 3","type":"related"},{"name":"childhood absence epilepsy caused by mutation in GABRG2","type":"exact"},{"name":"epilepsy, childhood absence, susceptibility to, 2","type":"related"},{"name":"epilepsy, childhood absence, susceptibility to, type 2","type":"related"},{"name":"generalised epilepsy with febrile seizures plus caused by mutation in GABRG2","type":"exact"},{"name":"generalised epilepsy with febrile seizures plus, type 3","type":"exact"},{"name":"generalized epilepsy with febrile seizures plus caused by mutation in GABRG2","type":"exact"},{"name":"generalized epilepsy with febrile seizures plus, type 3","type":"exact"},{"name":"susceptibility to childhood absence epilepsy 2","type":"related"}],"termid":"MONDO:0011891","xrefs":{"Monarch":{"xref_id":"0011891"}}}


id: PBO:0013108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ergothioneine biosynthesis protein Egt1","termid":"PBO:0013108"}


id: GO:0046930
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex providing a discrete opening in a membrane that allows the passage of gases and/or liquids.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"pore complex","synonyms":[{"name":"channel-forming toxin activity","type":"related"},{"name":"pore","type":"exact"},{"name":"pore-forming toxin activity","type":"related"}],"termid":"GO:0046930"}


id: PBO:0090733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomerase regulatory factor Ctr1","termid":"PBO:0090733"}


id: FYPO:0000733
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the mitotic spindle is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long spindle","termid":"FYPO:0000730"},{"relation_name":"is_a","term_name":"abnormal bipolar mitotic spindle","termid":"FYPO:0001574"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002399"}],"interesting_parent_ids":["FYPO:0002399","FYPO:0001985","FYPO:0000054","FYPO:0000120","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"long mitotic spindle","synonyms":[{"name":"elongated mitotic spindle","type":"exact"},{"name":"increased mitotic spindle length","type":"exact"},{"name":"long bipolar mitotic spindle","type":"exact"},{"name":"long mitotic spindle during vegetative growth","type":"exact"},{"name":"long mitotic spindles","type":"exact"},{"name":"long spindle during mitosis","type":"exact"},{"name":"long spindle during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000733"}


id: MONDO:0017249
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital pulmonary airway malformation","termid":"MONDO:0016580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital pulmonary airway malformation type 1","secondary_identifiers":["GARD:21094","Orphanet:280832","UMLS:C5437763","icd11.foundation:1455719613","MEDGEN:1760964"],"synonyms":[{"name":"CCAM type 1","type":"exact"},{"name":"CPAM type 1","type":"exact"},{"name":"congenital cystic adenomatoid malformation of the lung type 1","type":"exact"},{"name":"congenital cystic adenomatous malformation of the lung type 1","type":"exact"},{"name":"congenital cystic disease of the lung type 1","type":"exact"}],"termid":"MONDO:0017249","xrefs":{"Monarch":{"xref_id":"0017249"}}}


id: PBO:0076624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin folding cofactor E like","termid":"PBO:0076624"}


id: PBO:0005022
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.3.1.16","termid":"PBO:0005022"}


id: PBO:0003613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoplasmic methionine-tRNA ligase Mrs1 (predicted)","termid":"PBO:0003613"}


id: PATO:0001076
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001076 relative momentum (obsolete PATO:0001076)","termid":"PATO:0001076"}


id: MONDO:0043364
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare abnormality of eosinophil granulocytes characterized by decreased or absent peroxidase activity and decreased volume of the granule matrix.","definition_xrefs":["OMIM:261500"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte disorder","termid":"MONDO:0004805"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0006025"],"is_obsolete":false,"name":"eosinophil peroxidase deficiency","secondary_identifiers":["GARD:12361","MESH:C564893","MEDGEN:342386","UMLS:C1850000","SCTID:711160007"],"synonyms":[{"name":"EPXD","type":"related"},{"name":"Presentey anomaly","type":"related"},{"name":"eosinophil peroxidase deficiency","type":"exact"},{"name":"eosinophil peroxidase deficiency, Partial","type":"related"},{"name":"eosinophil peroxidase deficiency, partial","type":"related"},{"name":"peroxidase and phospholipid deficiency in eosinophils","type":"related"},{"name":"presentey anomaly","type":"related"}],"termid":"MONDO:0043364","xrefs":{"Monarch":{"xref_id":"0043364"}}}


id: MONDO:0008741
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies.","definition_xrefs":["Orphanet:991"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAGOD syndrome","secondary_identifiers":["MEDGEN:347985","SCTID:722132007","UMLS:C1859967","MESH:C537018","GARD:3086","OMIM:202660"],"synonyms":[{"name":"Kennerknecht sorgo Oberhoffer syndrome","type":"related"},{"name":"PAGOD syndrome","type":"exact"},{"name":"agonadism with multiple internal malformations","type":"related"},{"name":"pulmonary hypoplasia, hypoplasia of the pulmonary artery, agonadism, omphalocele-diaphragmatic defect, and dextrocardia","type":"related"},{"name":"pulmonary hypoplasia-agonadism-dextrocardia-diaphragmatic hernia syndrome","type":"exact"}],"termid":"MONDO:0008741","xrefs":{"Monarch":{"xref_id":"0008741"}}}


id: GO:0051273
data:
  {"annotated_genes":["SJAG_00876","SJAG_03587","SJAG_04659","SJAG_04666","SJAG_01255","SJAG_01787","SJAG_03123","SJAG_05001","SJAG_04462","SJAG_04483","SJAG_01290","SJAG_01453","SJAG_05285","SJAG_02446","SJAG_02192","SJAG_02590","SJAG_01288","SJAG_04771","SJAG_04509","SJAG_00610","SJAG_03646","SJAG_04668","SJAG_01171","SJAG_01835","SJAG_02222","SJAG_03705","SJAG_00218","SJAG_04073"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76602,74932,63285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006078"},{"annotations":[94223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034413"},{"annotations":[72795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034412"},{"annotations":[105864,115562,72797,91359,70582,74275,75565,112908],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071970"},{"annotations":[77951,102394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070880"},{"annotations":[94861,107819,101696,101697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070879"},{"annotations":[87281,92184],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0140748"},{"annotations":[87658],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032951"},{"annotations":[102597,92168,117651,117776,105677,90533,105106],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090334"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving beta-glucans, compounds composed of glucose residues linked by beta-D-glucosidic bonds.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucan metabolic process","termid":"GO:0044042"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00218":null,"SJAG_00610":null,"SJAG_00876":null,"SJAG_01171":null,"SJAG_01255":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01453":null,"SJAG_01787":null,"SJAG_01835":null,"SJAG_02192":null,"SJAG_02222":null,"SJAG_02446":null,"SJAG_02590":null,"SJAG_03123":null,"SJAG_03587":null,"SJAG_03646":null,"SJAG_03705":null,"SJAG_04073":null,"SJAG_04462":null,"SJAG_04483":null,"SJAG_04509":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04771":null,"SJAG_05001":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"beta-glucan metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"beta-glucan metabolism","type":"exact"}],"termid":"GO:0051273","terms_by_termid":{"GO:0006078":null,"GO:0032951":null,"GO:0034412":null,"GO:0034413":null,"GO:0070879":null,"GO:0070880":null,"GO:0071970":null,"GO:0090334":null,"GO:0140748":null}}


id: PBO:0031813
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_autophagy","termid":"PBO:0031813"}


id: PBO:0054052
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 1394","termid":"PBO:0054052"}


id: GO:1901235
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of (R)-carnitine from one side of a membrane to the other.","definition_xrefs":["PMID:20357772","PMID:20829798","PMID:16365042","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carnitine transmembrane transporter activity","termid":"GO:0015226"}],"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:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"(R)-carnitine transmembrane transporter activity","termid":"GO:1901235"}


id: FYPO:0005061
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of the serine residue at position 5 within one or more copies of the heptapeptide repeat (YSPTSPS) of the C-terminal domain of RNA polymerase II normal (i.e. indistinguishable from wild type).","definition_xrefs":["GO:0071620","PomBase:mah","PMID:17502918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein phosphorylation during vegetative growth","termid":"FYPO:0000776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal phosphorylation of RNA polymerase II C-terminal domain serine 5 residues during vegetative growth","synonyms":[{"name":"normal phosphorylation of RNA polymerase II C-terminal domain serine 5 residues during mitotic cell cycle","type":"related"},{"name":"normal phosphorylation of RNA polymerase II CTD serine 5 residues during vegetative growth","type":"exact"}],"termid":"FYPO:0005061"}


id: SO:0001551
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that increases the rate of transcription with respect to a reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rate_of_transcription_variant","termid":"SO:0001550"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased_transcription_rate_variant","synonyms":[{"name":"increased transcription rate variant","type":"exact"}],"termid":"SO:0001551"}


id: MONDO:0000059
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete methylmalonic aciduria and homocystinuria (obsolete MONDO:0000059)","termid":"MONDO:0000059","xrefs":{"Monarch":{"xref_id":"0000059"}}}


id: GO:0071762
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of two identical immunoglobulin heavy chains of the IgNAR isotype held together by disulfide bonds and lacking immunoglobulin light chains.","definition_xrefs":["PMID:16051357","ISBN:0781765196","PMID:12543123","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin complex","termid":"GO:0019814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"heavy chain immunoglobulin complex","synonyms":[{"name":"HCab","type":"narrow"},{"name":"Ig NAR immunoglobulin complex","type":"narrow"},{"name":"IgNAR antibody","type":"narrow"},{"name":"IgNAR immunoglobulin complex","type":"narrow"}],"termid":"GO:0071762"}


id: GO:0001524
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. The colorless and basic protein moiety of hemoglobin and myoglobins.","definition_xrefs":["GOC:ai","ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete globin (obsolete GO:0001524)","synonyms":[{"name":"globin","type":"exact"}],"termid":"GO:0001524"}


id: MONDO:0019892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the short arm of chromosome 7","termid":"MONDO:0016889"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal monosomy 7p","secondary_identifiers":["GARD:19325","Orphanet:96126","UMLS:C5190515","MEDGEN:1683031"],"synonyms":[{"name":"distal deletion 7p","type":"exact"},{"name":"distal monosomy type 7p","type":"exact"},{"name":"monosomy 7pter","type":"exact"},{"name":"telomeric deletion 7p","type":"exact"}],"termid":"MONDO:0019892","xrefs":{"Monarch":{"xref_id":"0019892"}}}


id: GO:0035989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a tendon over time, from its formation to the mature structure. A tendon is a fibrous, strong, connective tissue that connects muscle to bone or integument and is capable of withstanding tension. Tendons and muscles work together to exert a pulling force.","definition_xrefs":["GOC:yaf","PMID:21412429","UBERON:0000043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connective tissue development","termid":"GO:0061448"}],"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":"tendon development","synonyms":[{"name":"sinew development","type":"related"}],"termid":"GO:0035989"}


id: GO:0030430
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The cytoplasm of a host cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host intracellular part","termid":"GO:0033646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell cytoplasm","secondary_identifiers":["GO:0097679"],"synonyms":[{"name":"other organism cytoplasm","type":"related"}],"termid":"GO:0030430"}


id: SO:0000473
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The gene product is involved in its own transcriptional regulation where it decreases transcription.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcriptionally_repressed","termid":"SO:0000126"},{"relation_name":"is_a","term_name":"autoregulated","termid":"SO:0000471"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negatively_autoregulated","synonyms":[{"name":"negatively autoregulated","type":"exact"}],"termid":"SO:0000473"}


id: PR:O74397
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An asparagine synthetase domain-containing protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03385"],"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":"asparagine synthetase domain-containing protein C4F6.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4F6.11c","secondary_identifiers":["UniProtKB:O74397"],"synonyms":[{"name":"Spom972h-ASNSD1","type":"exact"}],"termid":"PR:O74397"}


id: PBO:0082367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAR domain protein that localizes to early and late Golgi vesicles; required for adaptation to varying nutrient concentrations, fluid-phase endocytosis, polarization of the actin cytoskeleton, and vacuole biogenesis","termid":"PBO:0082367"}


id: GO:0014835
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized satellite cell acquires specialized features of a myoblast. This occurs as part of skeletal muscle regeneration. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["GOC:ef","GOC:mtg_muscle","PMID:16607119","CL:0000056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myoblast differentiation","termid":"GO:0045445"},{"relation_name":"part_of","term_name":"skeletal muscle tissue regeneration","termid":"GO:0043403"}],"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":"myoblast differentiation involved in skeletal muscle regeneration","termid":"GO:0014835"}


id: PBO:0061969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily AH member 1 pseudogene","termid":"PBO:0061969"}


id: GO:0036185
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 15-oxo-(5S,6R)-dihydroxy-(7E,9E,11Z,13E)-eicosatetraenoate + NADH + H+ = 15-oxo-(5S,6R)-dihydroxy-(7E,9E,11Z)-eicosatrienoate + NAD+.","definition_xrefs":["PMID:10837478","RHEA:41592"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"13-lipoxin reductase activity","secondary_identifiers":["Reactome:R-HSA-2161844"],"termid":"GO:0036185"}


id: MONDO:0015949
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic subcutaneous tissue disorder (obsolete MONDO:0015949)","secondary_identifiers":["Orphanet:183484"],"synonyms":[{"name":"genetic subcutaneous tissue disorder","type":"related"}],"termid":"MONDO:0015949","xrefs":{"Monarch":{"xref_id":"0015949"}}}


id: GO:0050643
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 10-deacetylbaccatin III + acetyl-CoA = baccatin III + CoA.","definition_xrefs":["RHEA:20137","EC:2.3.1.167"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetyltransferase activity","termid":"GO:0016413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016746"],"is_obsolete":false,"name":"10-deacetylbaccatin III 10-O-acetyltransferase activity","secondary_identifiers":["MetaCyc:2.3.1.167-RXN","KEGG_REACTION:R06311"],"synonyms":[{"name":"acetyl-CoA:taxan-10beta-ol O-acetyltransferase","type":"broad"}],"termid":"GO:0050643"}


id: MONDO:0001207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute respiratory failure","termid":"MONDO:0001208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neonatal respiratory failure","secondary_identifiers":["ICD9:770.84","UMLS:C0521648","DOID:11161","ICD10CM:P28.5","MEDGEN:105483","SCTID:95619009"],"synonyms":[{"name":"respiratory failure of newborn","type":"exact"}],"termid":"MONDO:0001207","xrefs":{"Monarch":{"xref_id":"0001207"}}}


id: PBO:0004977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RecQ type DNA helicase Tlh1","termid":"PBO:0004977"}


id: MONDO:0024990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diseases of domestic swine and of the wild boar of the genus Sus.","definition_xrefs":["MESH:D013553"],"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":"swine disease","synonyms":[{"name":"disease, swine","type":"related"},{"name":"diseases, swine","type":"related"},{"name":"swine disease","type":"exact"}],"termid":"MONDO:0024990","xrefs":{"Monarch":{"xref_id":"0024990"}}}


id: PBO:0001114
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.2.1.36","termid":"PBO:0001114"}


id: MONDO:0021420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic polypoid swelling of the vocal cord mucosa. It is usually unilateral and caused by excessive use of the voice.","definition_xrefs":["NCIT:C3440"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laryngeal disorder","termid":"MONDO:0004382"},{"relation_name":"is_a","term_name":"polyp","termid":"MONDO:0005079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyp of vocal cord","secondary_identifiers":["icd11.foundation:1351291002","UMLS:C0042929","MEDGEN:21887","SCTID:9078005","EFO:0009478"],"synonyms":[{"name":"laryngeal vocal fold polyp","type":"exact"},{"name":"polyp of the vocal cord","type":"exact"},{"name":"vocal cord polyp","type":"exact"}],"termid":"MONDO:0021420","xrefs":{"Monarch":{"xref_id":"0021420"}}}


id: GO:0019191
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of cellobiose from one side of a membrane to the other. Cellobiose, or 4-O-beta-D-glucopyranosyl-D-glucose, is a disaccharide that represents the basic repeating unit of cellulose.","definition_xrefs":["ISBN:0198506732","ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disaccharide transmembrane transporter activity","termid":"GO:0015154"}],"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:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"cellobiose transmembrane transporter activity","secondary_identifiers":["GO:0019190"],"synonyms":[{"name":"cellobiose permease activity","type":"exact"}],"termid":"GO:0019191"}


id: MONDO:0014906
data:
  {"annotated_genes":["SJAG_00031"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85912],"is_not":false,"summary":null,"term":"MONDO:0014906"}]},"cv_name":"mondo","definition":"An autosomal recessive sub-type of Charcot-Marie-Tooth disease caused by compound heterozygous or homozygous mutation(s) in the MFN2 gene, encoding mitofusin-2. This condition is more severe and has an earlier onset as compared to Charcot-Marie-Tooth disease type 2A2A.","definition_xrefs":["NCIT:C150647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00031":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, axonal, autosomal recessive, type 2a2b;","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:934692","OMIM:617087","DOID:0111557","UMLS:C4310725"],"synonyms":[{"name":"CMT2A2B","type":"related"},{"name":"Charcot-Marie-Tooth disease type 2A2B","type":"exact"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2A2B","type":"exact"}],"termid":"MONDO:0014906","terms_by_termid":{"MONDO:0014906":null},"xrefs":{"Monarch":{"xref_id":"0014906"}}}


id: MONDO:1011060
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polycystic kidney disease that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polycystic kidney disease, non-human animal","termid":"MONDO:1010262"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polycystic kidney disease, sheep","secondary_identifiers":["OMIA:000807-9940"],"termid":"MONDO:1011060","xrefs":{"Monarch":{"xref_id":"1011060"}}}


id: MONDO:0002200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign, slow-growing and painless neoplasm of sweat glands. It usually arises in the head and neck. It is characterized by the presence of a mesenchymal chondroid stroma, fibrosis, and epithelial structures.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eccrine sweat gland neoplasm","termid":"MONDO:0002090"},{"relation_name":"is_a","term_name":"mixed neoplasm","termid":"MONDO:0021043"}],"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":"eccrine mixed tumor of skin","secondary_identifiers":["SCTID:254720009","EFO:1000385","MONDO:0006308","DOID:2079","MEDGEN:91074","NCIT:C4474","UMLS:C0346026"],"synonyms":[{"name":"benign mixed tumor of skin","type":"exact"},{"name":"benign mixed tumor of skin (chondroid syringoma)","type":"exact"},{"name":"benign mixed tumor of the skin","type":"exact"},{"name":"benign mixed tumor of the skin (chondroid syringoma)","type":"exact"},{"name":"benign mixed tumour of skin","type":"exact"},{"name":"benign mixed tumour of skin (chondroid syringoma)","type":"exact"},{"name":"benign mixed tumour of the skin","type":"exact"},{"name":"benign mixed tumour of the skin (chondroid syringoma)","type":"exact"},{"name":"chondroid syringoma","type":"exact"},{"name":"eccrine mixed tumor","type":"exact"},{"name":"eccrine mixed tumor (morphologic abnormality)","type":"exact"},{"name":"eccrine mixed tumour","type":"exact"},{"name":"eccrine mixed tumour (morphologic abnormality)","type":"exact"},{"name":"eccrine sweat gland mixed neoplasm","type":"exact"},{"name":"mixed eccrine neoplasm of the skin","type":"exact"},{"name":"mixed tumor of the skin (chondroid syringoma)","type":"exact"},{"name":"mixed tumour of the skin (chondroid syringoma)","type":"exact"}],"termid":"MONDO:0002200","xrefs":{"Monarch":{"xref_id":"0002200"}}}


id: MONDO:0014135
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary pulmonary hypertension in which the cause of the disease is a mutation in the CAV1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heritable pulmonary arterial hypertension","termid":"MONDO:0017148"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary hypertension, primary, 3","secondary_identifiers":["MEDGEN:815522","UMLS:C3809192","OMIM:615343"],"synonyms":[{"name":"CAV1 primary pulmonary hypertension","type":"exact"},{"name":"PPH3","type":"related"},{"name":"primary pulmonary hypertension caused by mutation in CAV1","type":"exact"},{"name":"pulmonary hypertension, primary, 3","type":"exact"},{"name":"pulmonary hypertension, primary, type 3","type":"exact"}],"termid":"MONDO:0014135","xrefs":{"Monarch":{"xref_id":"0014135"}}}


id: GO:0098023
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The basal end of the virus tail, which is used by the virus to attach to the host cell.","definition_xrefs":["GOC:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"virion component","termid":"GO:0044423"},{"relation_name":"part_of","term_name":"virus tail","termid":"GO:0098015"}],"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":"virus tail, tip","synonyms":[{"name":"bacteriophage tail tip","type":"narrow"}],"termid":"GO:0098023"}


id: GO:0021502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the lateral borders of the neural plate begin to migrate upwards to form the neural folds, caused by the proliferation of the underlying mesoderm.","definition_xrefs":["GO_REF:0000021","GOC:jid","PMID:15806586","GOC:dph","GOC:cls","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"neural fold formation","termid":"GO:0001842"}],"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 fold elevation formation","termid":"GO:0021502"}


id: FYPO:0005691
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the mitotic spindle pole body (SPB) moves rapidly back and forth to a lower extent and over a smaller area than normal, causing decreased chromosome movement. Normally, SPB oscillation occurs during mitotic interphase (as well as prophase) but is restricted to a small space.","definition_xrefs":["PMID:12390246","PMID:19001497","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body-led chromosome movement during mitotic interphase","termid":"FYPO:0005348"},{"relation_name":"is_a","term_name":"decreased microtubule-based movement during vegetative growth","termid":"FYPO:0005462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"decreased spindle pole body-led chromosome movement during mitotic interphase","synonyms":[{"name":"decreased mitotic SPB oscillation during mitotic interphase","type":"exact"},{"name":"decreased mitotic spindle pole body movement during mitotic interphase","type":"exact"},{"name":"decreased mitotic spindle pole body oscillation during mitotic interphase","type":"exact"},{"name":"decreased spindle pole body-led chromosome movement during interphase of mitotic cell cycle","type":"related"},{"name":"decreased spindle pole body-led chromosome movement during mitotic interphase during vegetative growth","type":"exact"},{"name":"reduced mitotic spindle pole body oscillation during mitotic interphase","type":"exact"}],"termid":"FYPO:0005691"}


id: GO:0019988
data:
  {"annotated_genes":["SJAG_05228"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71076],"is_not":false,"summary":null,"term":"GO:0019988"}]},"cv_name":"biological_process","definition":"The covalent alteration of an amino acid charged on a tRNA before it is incorporated into a protein, as in N-formylmethionine, selenocysteine or pyrrolysine.","definition_xrefs":["GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA modification","termid":"GO:0006400"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05228":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006399"],"is_obsolete":false,"name":"charged-tRNA amino acid modification","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0030630"],"synonyms":[{"name":"charged tRNA amino acid modification","type":"exact"},{"name":"charged tRNA modification","type":"exact"},{"name":"charged-tRNA modification","type":"related"},{"name":"pre-translational amino acid modification","type":"exact"},{"name":"pre-translational protein modification","type":"exact"},{"name":"pretranslation protein modification","type":"exact"},{"name":"pretranslational amino acid modification","type":"exact"}],"termid":"GO:0019988","terms_by_termid":{"GO:0019988":null}}


id: PBO:0089031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial pyruvate dehydrogenase (lipoamide) kinase Pkp1","termid":"PBO:0089031"}


id: GO:0038087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by vascular endothelial growth factor (VEGF) binding to an alpha-type platelet-derived growth factor receptor (PDGFR) on the surface of a cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:17470632","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"platelet-derived growth factor receptor-alpha signaling pathway","termid":"GO:0035790"},{"relation_name":"is_a","term_name":"VEGF-activated platelet-derived growth factor receptor signaling pathway","termid":"GO:0038086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"VEGF-activated platelet-derived growth factor receptor-alpha signaling pathway","synonyms":[{"name":"VEGF-A/PDGFRalpha signaling","type":"narrow"},{"name":"VEGF-activated PDGFRalpha signalling pathway","type":"exact"},{"name":"VEGF-activated platelet-derived growth factor receptor-alpha signalling pathway","type":"exact"},{"name":"VEGF/PDGFRalpha signaling pathway","type":"exact"},{"name":"vascular endothelial growth factor-activated platelet-derived growth factor receptor-alpha signaling pathway","type":"exact"}],"termid":"GO:0038087"}


id: PBO:0036407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaxin 2 Mtx2 (predicted)","termid":"PBO:0036407"}


id: MONDO:0006094
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primitive neuroectodermal tumor (small round blue cell tumor) of the thorax which can involve the periosteum, thoracic wall and/or pleura though it spares the lung parenchyma.","definition_xrefs":["NCIT:C7542"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thoracic cancer","termid":"MONDO:0003274"},{"relation_name":"is_a","term_name":"peripheral primitive neuroectodermal tumor","termid":"MONDO:0018271"}],"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":"Askin tumor","secondary_identifiers":["UMLS:C0877849","DOID:0050608","MEDGEN:209112","ICDO:9365/3","MESH:C563168","EFO:1000095"],"synonyms":[{"name":"Askin tumor","type":"exact"},{"name":"Askin's tumor","type":"exact"},{"name":"Askin's tumour","type":"exact"},{"name":"PNET of thoracopulmonary region","type":"exact"},{"name":"peripheral neuroectodermal tumor of thoracopulmonary region","type":"exact"},{"name":"peripheral neuroectodermal tumour of thoracopulmonary region","type":"exact"},{"name":"small cell tumor of thoracopulmonary region","type":"exact"},{"name":"small cell tumour of thoracopulmonary region","type":"exact"}],"termid":"MONDO:0006094","xrefs":{"Monarch":{"xref_id":"0006094"}}}


id: PBO:0073053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCY1 like pseudokinase 1","termid":"PBO:0073053"}


id: MONDO:0008500
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":"striae distensae, familial","secondary_identifiers":["MESH:C566104","MEDGEN:348875","OMIM:185200","UMLS:C1861447"],"synonyms":[{"name":"striae distensae, familial","type":"exact"}],"termid":"MONDO:0008500","xrefs":{"Monarch":{"xref_id":"0008500"}}}


id: MONDO:0024326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign neoplasm that arises from the mesothelial cells of the pleura. It is characterized by a proliferation of epithelioid cells forming glandular and tubular patterns in a fibrous stroma.","definition_xrefs":["NCIT:C4499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign mesothelioma","termid":"MONDO:0002373"},{"relation_name":"is_a","term_name":"pleural mesothelioma","termid":"MONDO:0003308"},{"relation_name":"is_a","term_name":"adenomatoid tumor","termid":"MONDO:0004230"},{"relation_name":"is_a","term_name":"benign neoplasm of pleura","termid":"MONDO:0021457"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleural adenomatoid tumor","secondary_identifiers":["UMLS:C0346112","MEDGEN:83408","Orphanet:675814"],"synonyms":[{"name":"benign mesothelioma of pleura","type":"exact"},{"name":"benign mesothelioma of the pleura","type":"exact"},{"name":"pleura adenomatoid tumor","type":"exact"},{"name":"pleura adenomatoid tumour","type":"exact"},{"name":"pleural adenomatoid tumor","type":"exact"},{"name":"pleural benign mesothelioma","type":"exact"},{"name":"pleural mesothelioma, benign","type":"exact"}],"termid":"MONDO:0024326","xrefs":{"Monarch":{"xref_id":"0024326"}}}


id: PBO:0031849
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-swollen_spore","termid":"PBO:0031849"}


id: GO:0002857
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of natural killer cell mediated immune response to a tumor cell.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of natural killer cell mediated immunity","termid":"GO:0002717"},{"relation_name":"is_a","term_name":"positive regulation of immune response to tumor cell","termid":"GO:0002839"},{"relation_name":"is_a","term_name":"regulation of natural killer cell mediated immune response to tumor cell","termid":"GO:0002855"},{"relation_name":"positively_regulates","term_name":"natural killer cell mediated immune response to tumor cell","termid":"GO:0002423"}],"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 natural killer cell mediated immune response to tumor cell","synonyms":[{"name":"activation of natural killer cell mediated immune response to tumor cell","type":"narrow"},{"name":"stimulation of natural killer cell mediated immune response to tumor cell","type":"narrow"},{"name":"up regulation of natural killer cell mediated immune response to tumor cell","type":"exact"},{"name":"up-regulation of natural killer cell mediated immune response to tumor cell","type":"exact"},{"name":"upregulation of natural killer cell mediated immune response to tumor cell","type":"exact"}],"termid":"GO:0002857"}


id: GO:0072182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of nephron tubule epithelial cell differentiation.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell differentiation involved in kidney development","termid":"GO:2000696"},{"relation_name":"regulates","term_name":"nephron tubule epithelial cell differentiation","termid":"GO:0072160"}],"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 nephron tubule epithelial cell differentiation","termid":"GO:0072182"}


id: MONDO:0014197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Combined immunodeficiency due to MALT1 deficiency is a rare, genetic form of primary immunodeficiency characterized by growth retardation, early recurrent pulmonary infections leading to bronchiectasis, inflammatory gastrointestinal disease, and other symptoms, such as rash, dermatitis, skin infections.","definition_xrefs":["Orphanet:397964"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"combined immunodeficiency","termid":"MONDO:0015131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"combined immunodeficiency due to MALT1 deficiency","secondary_identifiers":["MEDGEN:815913","OMIM:615468","UMLS:C3809583","GARD:17647","DOID:0111988"],"synonyms":[{"name":"IMD12","type":"related"},{"name":"combined immunodeficiency due to MALT1 deficiency","type":"exact"},{"name":"immunodeficiency 12","type":"related"},{"name":"immunodeficiency type 12","type":"exact"}],"termid":"MONDO:0014197","xrefs":{"Monarch":{"xref_id":"0014197"}}}


id: PBO:0056631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 11","termid":"PBO:0056631"}


id: PATO:0002285
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Branchiness quality inhering in a bearer by virtue of increasing the degree to which there are subdivisions or offshoots in a bearer entity.","definition_xrefs":["PATOC:CVS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branched","termid":"PATO:0000402"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased branchiness","termid":"PATO:0002285"}


id: PBO:0001491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Msa1","termid":"PBO:0001491"}


id: GO:0070433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of the nucleotide-binding oligomerization domain containing 2 (NOD2) pathway.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway","termid":"GO:0070425"},{"relation_name":"is_a","term_name":"regulation of nucleotide-binding oligomerization domain containing 2 signaling pathway","termid":"GO:0070432"},{"relation_name":"negatively_regulates","term_name":"nucleotide-binding oligomerization domain containing 2 signaling pathway","termid":"GO:0070431"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of nucleotide-binding oligomerization domain containing 2 signaling pathway","synonyms":[{"name":"negative regulation of NOD2 signaling pathway","type":"exact"},{"name":"negative regulation of nucleotide-binding oligomerization domain containing 2 signalling pathway","type":"exact"}],"termid":"GO:0070433"}


id: PBO:0003662
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RITS complex subunit 3","termid":"PBO:0003662"}


id: GO:2000689
data:
  {"annotated_genes":["SJAG_02864","SJAG_04621","SJAG_04498","SJAG_00938"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97783,98043,89087,107885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071520"},{"annotations":[77211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903479"}]},"cv_name":"biological_process","definition":"An actin filament organization process that contributes to actomyosin contractile ring assembly during cytokinesis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament organization","termid":"GO:0007015"},{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"part_of","term_name":"actomyosin contractile ring assembly","termid":"GO:0000915"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_02864":null,"SJAG_04498":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0007049","GO:0030036","GO:0007010"],"is_obsolete":false,"name":"actomyosin contractile ring assembly actin filament organization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"actin filament organisation of constriction ring assembly","type":"related"},{"name":"actin filament organisation of contractile ring assembly","type":"exact"},{"name":"actin filament organisation of cytokinesis, actomyosin contractile ring assembly","type":"exact"},{"name":"actin filament organisation of cytokinesis, actomyosin contractile ring formation","type":"related"},{"name":"actin filament organisation of cytokinesis, actomyosin ring biosynthesis","type":"related"},{"name":"actin filament organisation of cytokinesis, actomyosin ring formation","type":"related"},{"name":"actin filament organisation of cytokinesis, contractile ring assembly","type":"related"},{"name":"actin filament organization involved in cytokinetic actomyosin contractile ring assembly","type":"exact"},{"name":"actin filament organization of constriction ring assembly","type":"related"},{"name":"actin filament organization of contractile ring assembly","type":"exact"},{"name":"actin filament organization of cytokinesis, actomyosin contractile ring assembly","type":"exact"},{"name":"actin filament organization of cytokinesis, actomyosin contractile ring formation","type":"related"},{"name":"actin filament organization of cytokinesis, actomyosin ring biosynthesis","type":"related"},{"name":"actin filament organization of cytokinesis, actomyosin ring formation","type":"related"},{"name":"actin filament organization of cytokinesis, contractile ring assembly","type":"related"},{"name":"regulation of actin filament localization of constriction ring assembly","type":"related"},{"name":"regulation of actin filament localization of contractile ring assembly","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, actomyosin contractile ring assembly","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, actomyosin contractile ring formation","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, actomyosin ring biosynthesis","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, actomyosin ring formation","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, contractile ring assembly","type":"related"}],"termid":"GO:2000689","terms_by_termid":{"GO:0071520":null,"GO:1903479":null}}


id: GO:0008153
data:
  {"annotated_genes":["SJAG_02408"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72782],"is_not":false,"summary":null,"term":"GO:0008153"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 4-aminobenzoate, an intermediate in the synthesis of folic acid, a compound which some organisms, e.g. prokaryotes, eukaryotic microbes, and plants, can synthesize de novo. Others, notably mammals, cannot. In yeast, it is present as a factor in the B complex of vitamins.","definition_xrefs":["PMID:11377864","MetaCyc:PWY-6543","ISBN:0198506732","PMID:11960743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid biosynthetic process","termid":"GO:0008652"},{"relation_name":"is_a","term_name":"aromatic amino acid family biosynthetic process","termid":"GO:0009073"},{"relation_name":"is_a","term_name":"para-aminobenzoic acid metabolic process","termid":"GO:0046482"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02408":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"4-aminobenzoate biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"4-aminobenzoic acid biosynthesis","type":"exact"},{"name":"4-aminobenzoic acid biosynthetic process","type":"exact"},{"name":"PABA biosynthesis","type":"exact"},{"name":"PABA biosynthetic process","type":"exact"},{"name":"p-aminobenzoic acid biosynthesis","type":"exact"},{"name":"p-aminobenzoic acid biosynthetic process","type":"exact"},{"name":"para-aminobenzoic acid anabolism","type":"exact"},{"name":"para-aminobenzoic acid biosynthesis","type":"exact"},{"name":"para-aminobenzoic acid biosynthetic process","type":"exact"},{"name":"para-aminobenzoic acid formation","type":"exact"},{"name":"para-aminobenzoic acid synthesis","type":"exact"},{"name":"vitamin Bx biosynthesis","type":"exact"},{"name":"vitamin Bx biosynthetic process","type":"exact"}],"termid":"GO:0008153","terms_by_termid":{"GO:0008153":null}}


id: PBO:0026768
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_uracil_import","termid":"PBO:0026768"}


id: MONDO:0023155
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibula aplasia complex brachydactyly","termid":"MONDO:0023155","xrefs":{"Monarch":{"xref_id":"0023155"}}}


id: GO:0033534
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of verbascose, the pentasaccharide beta-D-fructofuranosyl alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"raffinose family oligosaccharide biosynthetic process","termid":"GO:0010325"},{"relation_name":"is_a","term_name":"verbascose metabolic process","termid":"GO:0033533"}],"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":"verbascose biosynthetic process","synonyms":[{"name":"verbascose anabolism","type":"exact"},{"name":"verbascose biosynthesis","type":"exact"},{"name":"verbascose formation","type":"exact"},{"name":"verbascose synthesis","type":"exact"}],"termid":"GO:0033534"}


id: MONDO:0017317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Phakomatosis pigmentokeratotica (PPK) is a very rare epidermal nevus disorder characterized by the association of speckled lentiginous nevi with epidermal sebaceous nevi, and extracutaneous anomalies.","definition_xrefs":["Orphanet:2874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system benign neoplasm","termid":"MONDO:0000648"},{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"is_a","term_name":"neurocutaneous syndrome","termid":"MONDO:0042983"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"},{"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:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"phakomatosis pigmentokeratotica","secondary_identifiers":["UMLS:C2931658","SCTID:723455009","MESH:C537893","GARD:4311","icd11.foundation:960559196","MEDGEN:419860"],"synonyms":[{"name":"Phacomatosis pigmentokeratotica","type":"related"},{"name":"organoid nevus with sebaceous differentiation, a speckled-lentiginous nevus, and other associated anomalies","type":"related"}],"termid":"MONDO:0017317","xrefs":{"Monarch":{"xref_id":"0017317"}}}


id: GO:0071665
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains gamma-catenin and TCF7L2 (TCF4), binds to the TCF DNA motif within a promoter element, and is involved in the regulation of WNT target gene transcription.","definition_xrefs":["GOC:BHF","GOC:vk","PMID:14661054"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catenin-TCF7L2 complex","termid":"GO:0071664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"gamma-catenin-TCF7L2 complex","synonyms":[{"name":"gamma-catenin-TCF4 complex","type":"exact"},{"name":"plakoglobin-TCF4 complex","type":"exact"}],"termid":"GO:0071665"}


id: PBO:0074335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1","termid":"PBO:0074335"}


id: PBO:0068978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 222, pseudogene","termid":"PBO:0068978"}


id: FYPO:0002802
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which a cell has a nucleus in an abnormal location at the cell cortex when the cell is subject to nitrogen starvation. The normal location is at the midpoint of the long axis of the cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized nucleus","termid":"FYPO:0002069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"nucleus mislocalized to cell cortex during nitrogen starvation","synonyms":[{"name":"nuclear displacement to cell cortex during nitrogen starvation","type":"exact"},{"name":"nucleus displaced to cell cortex during nitrogen starvation","type":"exact"},{"name":"nucleus mislocalised to cell cortex during nitrogen starvation","type":"exact"},{"name":"nucleus mislocalized to cell cortex during nitrogen depletion","type":"exact"},{"name":"nucleus mislocalized to cell cortex during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0002802"}


id: PATO:0000867
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000867 swallowing reflex value (obsolete PATO:0000867)","termid":"PATO:0000867"}


id: PBO:0052867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 5-10","termid":"PBO:0052867"}


id: GO:2000158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ubiquitin-specific protease (deubiquitinase) activity.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of peptidase activity","termid":"GO:0010952"},{"relation_name":"is_a","term_name":"regulation of ubiquitin-specific protease activity","termid":"GO:2000152"}],"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 ubiquitin-specific protease activity","synonyms":[{"name":"positive regulation of UBP","type":"related"},{"name":"positive regulation of UCH2","type":"related"},{"name":"positive regulation of deubiquitinase activity","type":"exact"},{"name":"positive regulation of ubiquitin hydrolase activity","type":"exact"}],"termid":"GO:2000158"}


id: MONDO:0012810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intracranial berry aneurysm","termid":"MONDO:0016483"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aneurysm, intracranial berry, 7","secondary_identifiers":["MESH:C567406","GARD:18325","DOID:0080970","MEDGEN:436919","OMIM:612161","UMLS:C2677337"],"synonyms":[{"name":"ANIB7","type":"exact"},{"name":"aneurysm, intracranial BERRY, 7","type":"related"}],"termid":"MONDO:0012810","xrefs":{"Monarch":{"xref_id":"0012810"}}}


id: PBO:0057482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR600 host gene","termid":"PBO:0057482"}


id: PBO:0076750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"teratocarcinoma-derived growth factor 1","termid":"PBO:0076750"}


id: MONDO:0043077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadism","termid":"MONDO:0002146"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"weinstein kliman scully syndrome","secondary_identifiers":["MEDGEN:419765","MESH:C536688","UMLS:C2931289","GARD:392"],"synonyms":[{"name":"cardiomyopathy, hypogonadism and metabolic anomalies","type":"related"},{"name":"primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities","type":"related"}],"termid":"MONDO:0043077","xrefs":{"Monarch":{"xref_id":"0043077"}}}


id: GO:0160222
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + D-alanine + D-serine = ADP + D-alanyl-D-serine + H+ + phosphate.","definition_xrefs":["EC:6.3.2.35","RHEA:27706"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-amino acid ligase activity","termid":"GO:0016881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"D-alanine-D-serine ligase activity","secondary_identifiers":["KEGG_REACTION:R09595","MetaCyc:RXN-11299"],"termid":"GO:0160222"}


id: PR:O94598
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sec5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94598"],"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":"exocyst complex component sec5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC622.10c","synonyms":[{"name":"Spom972h-sec5","type":"exact"}],"termid":"PR:O94598"}


id: MONDO:0009066
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nephropathic juvenile cystinosis is the intermediate form, in regards to severity and age of onset, of cystinosis, a metabolic disease characterized by an accumulation of cystine inside the lysosomes that causes damage in different organs and tissues, particularly in the kidneys and eyes.","definition_xrefs":["Orphanet:411634"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete nephropathy secondary to a storage or other metabolic disease (obsolete MONDO:0019743)","termid":"MONDO:0019743"},{"relation_name":"is_a","term_name":"inborn disorder of amino acid transport","termid":"MONDO:0019216"},{"relation_name":"is_a","term_name":"nephropathic cystinosis","termid":"MONDO:0100151"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0002561","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"juvenile nephropathic cystinosis","secondary_identifiers":["GARD:17685","UMLS:C0268626","MEDGEN:75701","SCTID:22830006","icd11.foundation:422905632","NANDO:2201235","MESH:C562683","ICD10EXP:E72.0+","OMIM:219900","ICD10EXP:N16.3*","NANDO:1200163"],"synonyms":[{"name":"cystinosis, intermediate","type":"related"},{"name":"cystinosis, late-onset juvenile or adolescent nephropathic","type":"exact"},{"name":"cystinosis, late-onset juvenile or adolescent nephropathic type","type":"related"},{"name":"intermediate cystinosis","type":"exact"},{"name":"juvenile cystinosis","type":"exact"},{"name":"juvenile nephropathic cystinosis","type":"exact"}],"termid":"MONDO:0009066","xrefs":{"Monarch":{"xref_id":"0009066"}}}


id: MONDO:0006040
data:
  {"annotated_genes":["SJAG_00547","SJAG_01524"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85468],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012557"},{"annotations":[86989],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009504"}]},"cv_name":"mondo","definition":"Metabolic acidosis characterized by the accumulation of lactate in the body. It is caused by tissue hypoxia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00547":null,"SJAG_01524":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"lactic acidosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1717","EFO:1000036","MESH:D000140","SCTID:91273001","UMLS:C0001125"],"termid":"MONDO:0006040","terms_by_termid":{"MONDO:0009504":null,"MONDO:0012557":null},"xrefs":{"Monarch":{"xref_id":"0006040"}}}


id: PBO:0054269
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 1655","termid":"PBO:0054269"}


id: PBO:0065679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidyl-tRNA hydrolase 1 homolog","termid":"PBO:0065679"}


id: PBO:0049904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hes family bHLH transcription factor 5","termid":"PBO:0049904"}


id: GO:0160067
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SIN signaling complex associated with the new mitotic spindle pole body during anaphase and characterized by the presence activated (GTP bound) GTPase (Spg1 in fission yeast) to activate SIN signaling.","definition_xrefs":["PMID:21131906"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SIN/MEN signaling complex","termid":"GO:0160065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"part_of","termid":"GO:0005816"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0015630","GO:0005816","GO:0032991"],"is_obsolete":false,"name":"new spindle pole body SIN signaling complex","synonyms":[{"name":"new spindle pole body SIN signalling complex","type":"exact"}],"termid":"GO:0160067"}


id: FYPO:0000140
data:
  {"alleles_by_uniquename":{"SJAG_00610:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00610","name":"pck2delta","uniquename":"SJAG_00610:allele-1"},"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"},"SJAG_01956:allele-1":{"allele_type":"amino_acid_mutation","description":"E405K ts","gene_uniquename":"SJAG_01956","name":"nuc2-1051","uniquename":"SJAG_01956:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_02621:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02621","name":"ago1delta","uniquename":"SJAG_02621:allele-1"},"SJAG_02796:allele-1":{"allele_type":"amino_acid_mutation","description":"A343T","gene_uniquename":"SJAG_02796","name":"pyk1-A343T","uniquename":"SJAG_02796:allele-1"},"SJAG_03118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03118","name":"leo1delta","uniquename":"SJAG_03118:allele-1"},"SJAG_03351:allele-1":{"allele_type":"amino_acid_mutation","description":"A186T ts","gene_uniquename":"SJAG_03351","name":"cut23-415","uniquename":"SJAG_03351:allele-1"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"},"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"},"SJAG_03940:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03940","name":"nem2delta","uniquename":"SJAG_03940: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-4":{"allele_type":"partial_amino_acid_deletion","description":"Pmk1 from S. pombe with deleted residues 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yeast cellular metabolism phenotype","type":"exact"}],"termid":"FYPO:0000140","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000006":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000207":null,"FYPO:0001038":null,"FYPO:0001327":null,"FYPO:0001838":null,"FYPO:0002033":null,"FYPO:0002678":null,"FYPO:0002680":null,"FYPO:0003727":null,"FYPO:0004165":null,"FYPO:0004205":null,"FYPO:0004573":null,"FYPO:0004982":null,"FYPO:0005957":null,"FYPO:0006989":null,"FYPO:0007363":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: MONDO:0019728
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-amyloid monoclonal immunoglobulin deposition disease","termid":"MONDO:0019463"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"heavy chain deposition disease","secondary_identifiers":["UMLS:C1333947","icd11.foundation:2018948190","NCIT:C7339","Orphanet:93556","GARD:19222","MEDGEN:232591"],"synonyms":[{"name":"HCDD","type":"exact"}],"termid":"MONDO:0019728","xrefs":{"Monarch":{"xref_id":"0019728"}}}


id: PBO:0055877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 3C","termid":"PBO:0055877"}


id: GO:0033141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the phosphorylation of a serine residue of a STAT (Signal Transducer and Activator of Transcription) protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of peptidyl-serine phosphorylation","termid":"GO:0033138"},{"relation_name":"is_a","term_name":"regulation of peptidyl-serine phosphorylation of STAT protein","termid":"GO:0033139"},{"relation_name":"positively_regulates","term_name":"serine phosphorylation of STAT protein","termid":"GO:0042501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of peptidyl-serine phosphorylation of STAT protein","secondary_identifiers":["GO:1903263"],"synonyms":[{"name":"activation of serine phosphorylation of STAT3 protein","type":"narrow"},{"name":"positive regulation of serine phosphorylation of STAT3 protein","type":"narrow"},{"name":"up regulation of serine phosphorylation of STAT3 protein","type":"narrow"},{"name":"up-regulation of serine phosphorylation of STAT3 protein","type":"narrow"},{"name":"upregulation of serine phosphorylation of STAT3 protein","type":"narrow"}],"termid":"GO:0033141"}


id: PBO:0079750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine-cytidine kinase 1","termid":"PBO:0079750"}


id: FYPO:0007525
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of ribosome binding by a gene product (usually a protein) in a mutant is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PMID:19625445","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding phenotype","termid":"FYPO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652"],"is_obsolete":false,"name":"decreased ribosome binding","synonyms":[{"name":"reduced ribosome binding","type":"exact"}],"termid":"FYPO:0007525"}


id: PBO:0003557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribose-phosphate pyrophosphokinase Prs5 (predicted)","termid":"PBO:0003557"}


id: GO:0110136
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The acquisition, loss, or modification of macromolecules within a protein-RNA complex, resulting in the alteration of an existing complex.","definition_xrefs":["GOC:rn","PMID:19737519","PMID:20542003","PMID:24240281"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex remodeling","termid":"GO:0034367"},{"relation_name":"is_a","term_name":"protein-RNA complex organization","termid":"GO:0071826"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein-RNA complex remodeling","synonyms":[{"name":"protein-RNA complex remodelling","type":"exact"}],"termid":"GO:0110136"}


id: MONDO:0000844
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spondyloepimetaphyseal dysplasia (obsolete MONDO:0000844)","termid":"MONDO:0000844","xrefs":{"Monarch":{"xref_id":"0000844"}}}


id: GO:1901084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of pyrrolizidine alkaloid.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"gene_count":0,"genotype_count":0,"name":"obsolete pyrrolizidine alkaloid catabolic process (obsolete GO:1901084)","synonyms":[{"name":"pyrrolizidine alkaloid breakdown","type":"exact"},{"name":"pyrrolizidine alkaloid catabolism","type":"exact"},{"name":"pyrrolizidine alkaloid degradation","type":"exact"}],"termid":"GO:1901084"}


id: PBO:0051123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 1/OR16-1 (pseudogene)","termid":"PBO:0051123"}


id: GO:0090361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of the appearance of any platelet-derived growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"platelet-derived growth factor production","termid":"GO:0090360"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of platelet-derived growth factor production","termid":"GO:0090361"}


id: PBO:0072184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S17","termid":"PBO:0072184"}


id: PBO:0038422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-2-macroglobulin","termid":"PBO:0038422"}


id: GO:1900150
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of defense response to fungus.","definition_xrefs":["PMID:22242006","GOC:dhl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to biotic stimulus","termid":"GO:0002831"},{"relation_name":"is_a","term_name":"regulation of defense response","termid":"GO:0031347"},{"relation_name":"is_a","term_name":"regulation of response to external stimulus","termid":"GO:0032101"},{"relation_name":"regulates","term_name":"defense response to fungus","termid":"GO:0050832"}],"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 defense response to fungus","secondary_identifiers":["GO:2000072"],"synonyms":[{"name":"regulation of defence response to fungi","type":"exact"},{"name":"regulation of defence response to fungus","type":"exact"},{"name":"regulation of defense response to fungi","type":"exact"},{"name":"regulation of defense response to fungi, incompatible interaction","type":"narrow"},{"name":"regulation of defense response to fungus, incompatible interaction","type":"narrow"},{"name":"regulation of resistance response to pathogenic fungi","type":"narrow"},{"name":"regulation of resistance response to pathogenic fungus","type":"narrow"},{"name":"regulation of response to pathogenic fungus (incompatible interaction)","type":"narrow"}],"termid":"GO:1900150"}


id: GO:2000249
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of actin cytoskeleton reorganization.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of actin cytoskeleton reorganization (obsolete GO:2000249)","synonyms":[{"name":"regulation of actin cytoskeleton remodeling","type":"exact"},{"name":"regulation of actin cytoskeleton reorganisation","type":"exact"}],"termid":"GO:2000249"}


id: GO:1990942
data:
  {"annotated_genes":["SJAG_01613","SJAG_02451","SJAG_01297","SJAG_01224","SJAG_02336"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93958,98378,98990,103650,108011],"is_not":false,"summary":null,"term":"GO:1990942"}]},"cv_name":"biological_process","definition":"A mechanism to recapture 'lost' chromosomes (chromosomes which have become detached from the spindle) during metaphase of mitotic chromosome segregation. Chromosomes with unattached kinetochores are migrated along (non polar) spindle microtubules to the mitotic spindle pole body by a combination of microtubule depolymerisation and 'kinetochore sliding' (migration of the chromosome along the microtubule). The chromosome subsequently migrates along the polar spindle microtubule to the metaphase plate.","definition_xrefs":["PMID:18256284"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of chromosome localization","termid":"GO:0051303"},{"relation_name":"part_of","term_name":"mitotic metaphase chromosome alignment","termid":"GO:0007080"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01224":null,"SJAG_01297":null,"SJAG_01613":null,"SJAG_02336":null,"SJAG_02451":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0000070"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0051179","GO:0000070","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"mitotic metaphase chromosome recapture","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1905185"],"synonyms":[{"name":"kinetochore retrieval","type":"exact"},{"name":"metaphase chromosome retrieval to the spindle pole body","type":"exact"},{"name":"microtubule sliding involved in kinetochore retrieval","type":"exact"},{"name":"microtubule sliding involved in metaphase chromosome retrieval to the spindle pole body","type":"exact"},{"name":"microtubule sliding involved in mitotic metaphase chromosome recapture","type":"related"},{"name":"microtubule sliding involved in sister kinetochore recapture","type":"exact"},{"name":"sister kinetochore recapture","type":"exact"}],"termid":"GO:1990942","terms_by_termid":{"GO:1990942":null}}


id: PBO:0004766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESCRT II complex subunit Vps36","termid":"PBO:0004766"}


id: GO:0060414
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the structure of the smooth muscle tissue surrounding the aorta is generated and organized. An aorta is an artery that carries blood from the heart to other parts of the body.","definition_xrefs":["Wikipedia:Aorta","GOC:bf","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle tissue morphogenesis","termid":"GO:0060415"},{"relation_name":"part_of","term_name":"aorta morphogenesis","termid":"GO:0035909"},{"relation_name":"part_of","term_name":"smooth muscle tissue development","termid":"GO:0048745"}],"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":"aorta smooth muscle tissue morphogenesis","termid":"GO:0060414"}


id: PBO:0078009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAF-type zinc finger domain containing 1","termid":"PBO:0078009"}


id: PR:P40901
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An asc-type amino acid transporter 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02267"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sexual differentiation process putative amino-acid permease isp5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1039.09","secondary_identifiers":["UniProtKB:P40901"],"synonyms":[{"name":"Spom972h-SLC7A10","type":"exact"}],"termid":"PR:P40901"}


id: MOD:01496
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"},{"relation_name":"is_a","term_name":"iTRAQ4plex-115 reporter+balance reagent acylated residue","termid":"MOD:01492"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter+balance reagent N-acylated residue","termid":"MOD:01709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ4plex-115 reporter+balance reagent N'-acylated histidine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"iTRAQ4plex115","type":"related"}],"termid":"MOD:01496"}


id: GO:0030889
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of B cell proliferation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of B cell proliferation","termid":"GO:0030888"},{"relation_name":"is_a","term_name":"negative regulation of lymphocyte proliferation","termid":"GO:0050672"},{"relation_name":"is_a","term_name":"negative regulation of B cell activation","termid":"GO:0050869"},{"relation_name":"negatively_regulates","term_name":"B cell proliferation","termid":"GO:0042100"}],"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 B cell proliferation","synonyms":[{"name":"down regulation of B cell proliferation","type":"exact"},{"name":"down-regulation of B cell proliferation","type":"exact"},{"name":"downregulation of B cell proliferation","type":"exact"},{"name":"inhibition of B cell proliferation","type":"narrow"},{"name":"negative regulation of B lymphocyte proliferation","type":"exact"},{"name":"negative regulation of B-cell proliferation","type":"exact"},{"name":"negative regulation of B-lymphocyte proliferation","type":"exact"}],"termid":"GO:0030889"}


id: MONDO:0006689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete carcinoid syndrome (obsolete MONDO:0006689)","secondary_identifiers":["NANDO:2200396"],"termid":"MONDO:0006689","xrefs":{"Monarch":{"xref_id":"0006689"}}}


id: PBO:0069567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 839, pseudogene","termid":"PBO:0069567"}


id: GO:2000895
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a hemicellulose.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemicellulose metabolic process","termid":"GO:0010410"},{"relation_name":"is_a","term_name":"cell wall polysaccharide catabolic process","termid":"GO:0044347"}],"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:0071554"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0071554"],"is_obsolete":false,"name":"hemicellulose catabolic process","synonyms":[{"name":"hemicellulose catabolism","type":"exact"}],"termid":"GO:2000895"}


id: PBO:0002340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH/NADPH dependent indole-3-acetaldehyde reductase AKR3C2","termid":"PBO:0002340"}


id: PBO:0063423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDE4B antisense RNA 1","termid":"PBO:0063423"}


id: MONDO:0019841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pituitary hormone defiency from vascular origin (obsolete MONDO:0019841)","secondary_identifiers":["Orphanet:95611","ICD10CM:E23.0"],"termid":"MONDO:0019841","xrefs":{"Monarch":{"xref_id":"0019841"}}}


id: GO:0051209
data:
  {"annotated_genes":["SJAG_03850"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061454"}]},"cv_name":"biological_process","definition":"The process in which calcium ions sequestered in the endoplasmic reticulum, Golgi apparatus or mitochondria are released into the cytosolic compartment.","definition_xrefs":["GOC:mtg_lung","GOC:hjd","GOC:dph","PMID:1814929"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of sequestering of calcium ion","termid":"GO:0051283"},{"relation_name":"is_a","term_name":"calcium ion transmembrane import into cytosol","termid":"GO:0097553"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03850":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"release of sequestered calcium ion into cytosol","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"calcium ion (Ca2+) mobilization","type":"broad"},{"name":"calcium mobilization","type":"broad"},{"name":"cytoplasmic release of sequestered calcium ion (Ca2+)","type":"broad"},{"name":"cytoplasmic release of stored calcium ion (Ca2+)","type":"broad"},{"name":"cytosolic release of sequestered calcium ion (Ca2+)","type":"exact"},{"name":"cytosolic release of stored calcium ion (Ca2+)","type":"exact"},{"name":"release of sequestered calcium ion (Ca2+)","type":"broad"},{"name":"release of sequestered calcium ion into cytoplasm","type":"broad"},{"name":"release of stored calcium ion (Ca2+)","type":"broad"},{"name":"release of stored calcium ion (Ca2+) into cytoplasm","type":"broad"},{"name":"release of stored calcium ion (Ca2+) into cytosol","type":"exact"}],"termid":"GO:0051209","terms_by_termid":{"GO:0061454":null}}


id: MONDO:0010970
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":"cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies","secondary_identifiers":["DOID:0111697","UMLS:C1832950","MEDGEN:318752","OMIM:600987","MESH:C563414"],"synonyms":[{"name":"CPCMR","type":"related"},{"name":"cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies","type":"exact"},{"name":"cleft palate, CARDIAC defects, and intellectual disability","type":"related"},{"name":"cleft palate, CARDIAC defects, and mental retardation","type":"related"},{"name":"cleft palate, Cardiac defects, and intellectual disability","type":"related"},{"name":"cleft palate, Cardiac defects, and mental retardation","type":"related"}],"termid":"MONDO:0010970","xrefs":{"Monarch":{"xref_id":"0010970"}}}


id: FYPO:0008258
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 cell surface is decreased. The cell surface refers to the external part of the cell wall and/or plasma membrane.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cell surface","termid":"FYPO:0002814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to cell surface","termid":"FYPO:0008258"}


id: GO:0048926
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the electrosensory lateral line system over time, from its formation to the mature structure.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lateral line system development","termid":"GO:0048925"}],"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":"electrosensory lateral line system development","termid":"GO:0048926"}


id: PATO:0002060
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"The specific wavelength of radiation that can be retained by a bearer.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"absorption quality","termid":"PATO:0001293"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"absorption wavelength","termid":"PATO:0002060"}


id: MOD:00930
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"tyrosine adduct with substrate analog inhibitor 1,2-dideoxy-2'-methyl-alpha-D-glucopyranoso-[2,1-d]-Delta2'-thiazoline.","definition_xrefs":["PubMed:15795231","Unimod:514"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"propyl-NAG tyrosine adduct","termid":"MOD:00930"}


id: GO:0032163
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A septin band, i.e. a diffuse ring composed of a series of septin bars running parallel to the long axis of the cell, located at the junction between the mother cell and the germ tube (hypha) of a fungal cell growing filamentously.","definition_xrefs":["PMID:16151244","GOC:mah","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septin band","termid":"GO:0032158"}],"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":"hyphal septin band","termid":"GO:0032163"}


id: GO:0003806
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the selective cleavage of Arg-Ile bonds in factor VII to form factor VIIa and factor XI to form factor XIa.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete coagulation factor XIIa activity (obsolete GO:0003806)","synonyms":[{"name":"activated beta blood-coagulation factor XII","type":"related"},{"name":"blood coagulation factor XII activity","type":"exact"},{"name":"blood-coagulation factor XIIabeta","type":"related"},{"name":"blood-coagulation factor XIIf","type":"related"},{"name":"coagulation factor XIIa activity","type":"exact"},{"name":"hageman factor (activated)","type":"related"},{"name":"hageman factor activity","type":"related"},{"name":"hageman factor beta-fragment","type":"related"},{"name":"hageman factor fragment HFf","type":"related"},{"name":"kallikreinogen activator","type":"related"},{"name":"prealbumin activator","type":"related"},{"name":"prekallikrein activator","type":"related"}],"termid":"GO:0003806"}


id: PBO:0063863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piezo type mechanosensitive ion channel component 1 pseudogene 2","termid":"PBO:0063863"}


id: PBO:0032767
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ark1 kinase consensus phosphorylation site is [RK]-X-[ST]","termid":"PBO:0032767"}


id: PBO:0047438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCF1 pseudogene 9","termid":"PBO:0047438"}


id: PBO:0059147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MPN domain containing","termid":"PBO:0059147"}


id: PBO:0060699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NDUFA4 mitochondrial complex associated","termid":"PBO:0060699"}


id: MONDO:1012419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"episodic falling, non-human animal","termid":"MONDO:1011885"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"episodic falling, dog","secondary_identifiers":["OMIA:001592-9615"],"termid":"MONDO:1012419","xrefs":{"Monarch":{"xref_id":"1012419"}}}


id: PBO:0054958
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 2372","termid":"PBO:0054958"}


id: PBO:0081129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFP1 zinc finger protein","termid":"PBO:0081129"}


id: PBO:0038807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 11","termid":"PBO:0038807"}


id: PBO:0079355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TUBA1B antisense RNA 1","termid":"PBO:0079355"}


id: PBO:0110976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily B member 6 (LAN blood group)","termid":"PBO:0110976"}


id: GO:0052909
data:
  {"annotated_genes":["SJAG_02821"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[68219],"is_not":false,"summary":null,"term":"GO:0052909"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 4 S-adenosyl-L-methionine + adenine(1779)/adenine(1780) in 18S rRNA = 4 S-adenosyl-L-homocysteine + N(6)-dimethyladenine(1779)/N(6)-dimethyladenine(1780) in 18S rRNA.","definition_xrefs":["RHEA:42780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA (adenine-N6,N6-)-dimethyltransferase activity","termid":"GO:0000179"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02821":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003824","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"18S rRNA (adenine(1779)-N(6)/adenine(1780)-N(6))-dimethyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["EC:2.1.1.183","MetaCyc:RXN-11634"],"synonyms":[{"name":"M(6)(2)A dimethylase activity","type":"broad"}],"termid":"GO:0052909","terms_by_termid":{"GO:0052909":null}}


id: GO:0047937
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 D-glucose 1-phosphate = D-glucose + D-glucose 1,6-bisphosphate.","definition_xrefs":["MetaCyc:GLUCOSE-1-PHOSPHATE-PHOSPHODISMUTASE-RXN","EC:2.7.1.41"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"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:0016301","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"glucose-1-phosphate phosphodismutase activity","secondary_identifiers":["RHEA:16397"],"synonyms":[{"name":"D-glucose-1-phosphate:D-glucose-1-phosphate 6-phosphotransferase activity","type":"related"},{"name":"glucose 1-phosphate transphosphorylase activity","type":"related"},{"name":"phosphodismutase activity","type":"related"}],"termid":"GO:0047937"}


id: PBO:0046010
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 5","termid":"PBO:0046010"}


id: GO:0140586
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Bridging together a cis-regulatory element and a terminator DNA sequences on the chromatin, holding two loop anchors together, maintaining a chromatin loop.","definition_xrefs":["PMID:19933151"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatin loop anchoring activity","termid":"GO:0140587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0060090","GO:0005488","GO:0003674","GO:0003677"],"is_obsolete":false,"name":"promoter-terminator loop anchoring activity","synonyms":[{"name":"terminator-promoter loop anchoring activity","type":"exact"}],"termid":"GO:0140586"}


id: PBO:0031637
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_gene_silencing","termid":"PBO:0031637"}


id: SO:0001189
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An oligo composed of LNA residues.","definition_xrefs":["RSC:cb"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"LNA","termid":"SO:0001188"},{"relation_name":"is_a","term_name":"synthetic_oligo","termid":"SO:0001247"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LNA_oligo","secondary_identifiers":["http://en.wikipedia.org/wiki/Locked_nucleic_acid"],"synonyms":[{"name":"LNA oligo","type":"exact"},{"name":"locked nucleic acid","type":"exact"}],"termid":"SO:0001189"}


id: FYPO:0003763
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell is inviable and contains one nucleus and no septum.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aseptate mononucleate vegetative cell","termid":"FYPO:0003785"},{"relation_name":"is_a","term_name":"inviable aseptate vegetative cell","termid":"FYPO:0003931"},{"relation_name":"is_a","term_name":"inviable mononucleate vegetative cell","termid":"FYPO:0006430"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000631","FYPO:0000032","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000004"],"is_obsolete":false,"name":"inviable aseptate mononucleate vegetative cell","synonyms":[{"name":"inviable aseptate mononucleate cell during vegetative growth","type":"exact"},{"name":"inviable aseptate mononucleate vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable mononucleate aseptate vegetative cell","type":"exact"},{"name":"inviable unseptated mononucleate vegetative cell","type":"exact"},{"name":"lethal; aseptate mononucleate vegetative cell","type":"exact"}],"termid":"FYPO:0003763"}


id: GO:0045939
data:
  {"annotated_genes":["SJAG_02104"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways involving steroids.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of steroid metabolic process","termid":"GO:0019218"},{"relation_name":"is_a","term_name":"negative regulation of lipid metabolic process","termid":"GO:0045833"},{"relation_name":"negatively_regulates","term_name":"steroid metabolic process","termid":"GO:0008202"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02104":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of steroid metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of steroid metabolic process","type":"exact"},{"name":"down-regulation of steroid metabolic process","type":"exact"},{"name":"downregulation of steroid metabolic process","type":"exact"},{"name":"inhibition of steroid metabolic process","type":"narrow"},{"name":"negative regulation of steroid metabolism","type":"exact"}],"termid":"GO:0045939","terms_by_termid":{"GO:0010895":null}}


id: PBO:0074274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schlafen like 1","termid":"PBO:0074274"}


id: PBO:0001304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic cohesin complex, non-SMC subunit Psc3","termid":"PBO:0001304"}


id: MONDO:0003881
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An apocrine adenocarcinoma that arises from the sweat glands in the vulva.","definition_xrefs":["NCIT:C40308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apocrine adenocarcinoma","termid":"MONDO:0003214"},{"relation_name":"is_a","term_name":"vulvar adenocarcinoma","termid":"MONDO:0024336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"vulvar apocrine adenocarcinoma","secondary_identifiers":["UMLS:C2202741","MEDGEN:384494","DOID:6448"],"synonyms":[{"name":"apocrine adenocarcinoma of mammalian vulva","type":"exact"},{"name":"mammalian vulva apocrine adenocarcinoma","type":"exact"},{"name":"vulvar apocrine adenocarcinoma","type":"exact"}],"termid":"MONDO:0003881","xrefs":{"Monarch":{"xref_id":"0003881"}}}


id: GO:0051436
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of ubiquitin ligase activity that contributes to the mitotic cell cycle.","definition_xrefs":["GOC:tb","GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle (obsolete GO:0051436)","synonyms":[{"name":"APC inhibition during mitotic cell cycle","type":"narrow"},{"name":"anaphase promoting complex inhibition during mitotic cell cycle","type":"narrow"},{"name":"anaphase-promoting complex inhibition during mitotic cell cycle","type":"narrow"},{"name":"down regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"down-regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"downregulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"inhibition of ubiquitin ligase activity during mitotic cell cycle","type":"narrow"},{"name":"mitotic APC inhibition","type":"narrow"},{"name":"mitotic APC inhibitor","type":"narrow"},{"name":"mitotic SCF complex inhibitor","type":"narrow"},{"name":"mitotic anaphase promoting complex inhibition","type":"narrow"},{"name":"mitotic anaphase promoting complex inhibitor","type":"narrow"},{"name":"mitotic anaphase-promoting complex inhibition","type":"narrow"},{"name":"mitotic anaphase-promoting complex inhibitor","type":"narrow"},{"name":"mitotic ubiquitin ligase inhibitor","type":"narrow"},{"name":"negative regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"negative regulation of ubiquitin-protein ligase activity during mitotic cell cycle","type":"related"}],"termid":"GO:0051436"}


id: PBO:0039035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 12, pseudogene","termid":"PBO:0039035"}


id: MONDO:0005103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A locally aggressive malignant neoplasm composed of mature adipocytes showing cell size variation and nuclear atypia. It is often associated with the presence of hyperchromatic multinucleated stromal cells, and varying numbers of lipoblasts. There are three histologic subtypes, sclerosing, inflammatory, and spindle cell liposarcoma. These tumors do not usually metastasize unless they undergo dedifferentiation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"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":"well-differentiated liposarcoma","secondary_identifiers":["ONCOTREE:WDLS","GARD:19721","ICDO:8851/3","MEDGEN:237164","UMLS:C1370889","NCIT:C4250","Orphanet:99971","EFO:0000736"],"synonyms":[{"name":"ALT","type":"exact"},{"name":"WDLS","type":"exact"},{"name":"atypical lipoma","type":"exact"},{"name":"atypical lipomatous tumor","type":"broad"},{"name":"atypical lipomatous tumour","type":"broad"},{"name":"well differentiated liposarcoma","type":"exact"},{"name":"well differentiated liposarcoma of deep soft tissue","type":"exact"},{"name":"well-differentiated liposarcoma","type":"exact"}],"termid":"MONDO:0005103","xrefs":{"Monarch":{"xref_id":"0005103"}}}


id: GO:0140314
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a calcium ion to prevent it from interacting with other partners or to inhibit its localization to the area of the cell or complex where it is active.","definition_xrefs":["PMID:13130076"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metal ion sequestering activity","termid":"GO:0140487"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140313"}],"interesting_parent_ids":["GO:0003674","GO:0140313"],"is_obsolete":false,"name":"calcium ion sequestering activity","termid":"GO:0140314"}


id: GO:0033358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of UDP-L-arabinose, uridinediphosphoarabinose, a substance composed of arabinose in glycosidic linkage with uridine diphosphate.","definition_xrefs":["MetaCyc:PWY-82","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar biosynthetic process","termid":"GO:0009226"},{"relation_name":"is_a","term_name":"UDP-L-arabinose metabolic process","termid":"GO:0033356"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"UDP-L-arabinose biosynthetic process","synonyms":[{"name":"UDP-L-arabinose anabolism","type":"exact"},{"name":"UDP-L-arabinose biosynthesis","type":"exact"},{"name":"UDP-L-arabinose formation","type":"exact"},{"name":"UDP-L-arabinose synthesis","type":"exact"}],"termid":"GO:0033358"}


id: PBO:0048984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPATCH11 pseudogene 1","termid":"PBO:0048984"}


id: PBO:0002901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyphosphate synthetase (predicted)","termid":"PBO:0002901"}


id: PBO:0051473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable (IV)-59 (pseudogene)","termid":"PBO:0051473"}


id: MONDO:0012772
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":"Stevenson-Carey syndrome","secondary_identifiers":["MEDGEN:383183","MESH:C567446","UMLS:C2677763","OMIM:611961"],"synonyms":[{"name":"Stevenson-Carey syndrome","type":"exact"}],"termid":"MONDO:0012772","xrefs":{"Monarch":{"xref_id":"0012772"}}}


id: PBO:0039514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 30B pseudogene 2","termid":"PBO:0039514"}


id: FYPO:0003210
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which a cell has a septum that is in an abnormal location and is not perpendicular to the long axis of the cell. The normal location is at the midpoint of the long axis of the cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized septum during vegetative growth","termid":"FYPO:0000339"},{"relation_name":"is_a","term_name":"misoriented septum during vegetative growth","termid":"FYPO:0001390"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0000032"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0005447","FYPO:0000631","FYPO:0000032"],"is_obsolete":false,"name":"mislocalized, misoriented septum","synonyms":[{"name":"abnormal septum localization and orientation","type":"related"},{"name":"abnormal septum location and orientation","type":"exact"},{"name":"abnormal septum position and orientation","type":"exact"},{"name":"abnormal septum positioning and orientation","type":"related"},{"name":"asymmetric, misoriented septum","type":"exact"},{"name":"asymmetrically located, misoriented septum","type":"exact"},{"name":"mislocalised, misoriented septum","type":"exact"},{"name":"mislocalized, misoriented septum during mitotic cell cycle","type":"related"},{"name":"mislocalized, misoriented septum during vegetative growth","type":"exact"},{"name":"misplaced, misoriented septum","type":"exact"}],"termid":"FYPO:0003210"}


id: GO:0043292
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Fibers, composed of actin, myosin, and associated proteins, found in cells of smooth or striated muscle.","definition_xrefs":["GOC:go_curators","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"},{"relation_name":"is_a","term_name":"supramolecular fiber","termid":"GO:0099512"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"contractile muscle fiber","synonyms":[{"name":"contractile fibre","type":"exact"}],"termid":"GO:0043292"}


id: MONDO:0001035
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypopyon","termid":"MONDO:0001036"}],"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":"hypopyon ulcer","secondary_identifiers":["ICD9:370.04","UMLS:C0155070","MEDGEN:509768","DOID:10442","SCTID:6395007"],"termid":"MONDO:0001035","xrefs":{"Monarch":{"xref_id":"0001035"}}}


id: GO:0102490
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 8-oxo-dGTP + 2 H2O = 8-oxo-dGMP + 2 hydrogenphosphate + 2 H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 8-oxo-dGTP phosphohydrolase activity (obsolete GO:0102490)","termid":"GO:0102490"}


id: PBO:0041866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase 12 (gene/pseudogene)","termid":"PBO:0041866"}


id: SO:0002292
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An mRNA that is generated by backsplicing of exons or introns, resulting in a covalently closed loop without a 5’ cap or 3’ polyA tail.","definition_xrefs":["PMID:29576969","PMID:29086764","PMID:29182528"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA","termid":"SO:0000234"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"circular_mRNA","synonyms":[{"name":"circular mRNA","type":"exact"},{"name":"coding circRNA","type":"exact"}],"termid":"SO:0002292"}


id: PR:Q9Y7X8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An actin-related protein 5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03309","PANTHER:PTHR11937:SF16"],"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":"actin-like protein arp5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC365.10","secondary_identifiers":["UniProtKB:Q9Y7X8"],"synonyms":[{"name":"Spom972h-ACTR5","type":"exact"}],"termid":"PR:Q9Y7X8"}


id: MONDO:0045053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, intermediate, or malignant bone-forming neoplasm. Representative examples include osteoma, osteoblastoma, and osteosarcoma.","definition_xrefs":["NCIT:C6603"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesenchymal cell neoplasm","termid":"MONDO:0002616"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteogenic neoplasm","secondary_identifiers":["MEDGEN:277453","UMLS:C1335146"],"synonyms":[{"name":"osseous neoplasm","type":"related"},{"name":"osseous tumor","type":"related"},{"name":"osseous tumour","type":"related"},{"name":"osteogenic neoplasm","type":"exact"},{"name":"osteogenic tumor","type":"exact"},{"name":"osteogenic tumour","type":"exact"}],"termid":"MONDO:0045053","xrefs":{"Monarch":{"xref_id":"0045053"}}}


id: PBO:0081169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger FYVE-type containing 1","termid":"PBO:0081169"}


id: GO:0033920
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 6-phospho-beta-D-galactoside + H2O = 6-phospho-D-galactose + an alcohol.","definition_xrefs":["RHEA:24568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"galactosidase activity","termid":"GO:0015925"}],"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:0016787"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016798","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"6-phospho-beta-galactosidase activity","secondary_identifiers":["MetaCyc:6-PHOSPHO-BETA-GALACTOSIDASE-RXN","EC:3.2.1.85"],"synonyms":[{"name":"6-phospho-beta-D-galactosidase activity","type":"related"},{"name":"6-phospho-beta-D-galactoside 6-phosphogalactohydrolase activity","type":"related"},{"name":"beta-D-phosphogalactoside galactohydrolase activity","type":"related"},{"name":"phospho-beta-D-galactosidase activity","type":"related"},{"name":"phospho-beta-galactosidase activity","type":"related"}],"termid":"GO:0033920"}


id: PBO:0089045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Cic1/Utp30 family","termid":"PBO:0089045"}


id: PBO:0003529
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Homolog Of Bin","termid":"PBO:0003529"}


id: PBO:0034522
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_arsenite","termid":"PBO:0034522"}


id: MONDO:0006782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Blood-filled uterus.","definition_xrefs":["MESH:D006409"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine disorder","termid":"MONDO:0002654"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemometra","secondary_identifiers":["MEDGEN:6776","SCTID:38280009","DOID:9958","UMLS:C0018948","ICD9:621.4","ICD10CM:N85.7"],"synonyms":[{"name":"hematometra","type":"exact"}],"termid":"MONDO:0006782","xrefs":{"Monarch":{"xref_id":"0006782"}}}


id: FYPO:0006553
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the nucleus is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization","termid":"FYPO:0003627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to nucleus","synonyms":[{"name":"normal protein localisation to nucleus","type":"exact"}],"termid":"FYPO:0006553"}


id: PBO:0050190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosome binding domain 1 pseudogene 7","termid":"PBO:0050190"}


id: GO:0060703
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of deoxyribonuclease.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclease inhibitor activity","termid":"GO:0140721"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0098772","GO:0004857","GO:0140678","GO:0003674","GO:0030234"],"is_obsolete":false,"name":"deoxyribonuclease inhibitor activity","synonyms":[{"name":"DNase inhibitor activity","type":"related"}],"termid":"GO:0060703"}


id: MONDO:0850049
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"painful legs and moving toes syndrome","secondary_identifiers":["GARD:12706","MEDGEN:1842291","Orphanet:617440","UMLS:C5680388"],"termid":"MONDO:0850049","xrefs":{"Monarch":{"xref_id":"0850049"}}}


id: PBO:0076331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SYS1-DBNDD2 readthrough (NMD candidate)","termid":"PBO:0076331"}


id: PBO:0001154
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"named from cerevisiae","termid":"PBO:0001154"}


id: PBO:0028712
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_global_homologous_chromosome_pairing","termid":"PBO:0028712"}


id: PBO:0072194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S17 pseudogene 11","termid":"PBO:0072194"}


id: GO:0032917
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of polyamines by addition of acetyl groups.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine metabolic process","termid":"GO:0006595"}],"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":"polyamine acetylation","termid":"GO:0032917"}


id: PATO:0002480
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in an bearer by virtue of the bearer's possessing only minor levels of ossification.","definition_xrefs":["PATOC:AD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ossified","termid":"PATO:0001448"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poorly ossified","termid":"PATO:0002480"}


id: GO:0061483
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cysteine sulfanate + GTP + IMP = sulfinylpropanyl adenylate + GDP + 3 H+ + phosphate.","definition_xrefs":["GOC:dph","PMID:8346915"],"gene_count":0,"genotype_count":0,"name":"obsolete sulfinylpropanyl adenylate synthase activity (obsolete GO:0061483)","synonyms":[{"name":"SPA synthase activity","type":"related"}],"termid":"GO:0061483"}


id: PBO:0070607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 75","termid":"PBO:0070607"}


id: PR:P32834
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sxa1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P32834"],"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":"aspartic proteinase sxa1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26A3.01","synonyms":[{"name":"Spom972h-sxa1","type":"exact"}],"termid":"PR:P32834"}


id: GO:0090233
data:
  {"annotated_genes":["SJAG_03126","SJAG_02336","SJAG_04259","SJAG_02169","SJAG_03353","SJAG_01679","SJAG_01297","SJAG_00883","SJAG_03681","SJAG_02451"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99350,113524,114011,106987,103647,90486,108006,111706,115643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[93960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"}]},"cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of the spindle checkpoint, a cell cycle checkpoint that delays the metaphase/anaphase transition until the spindle is correctly assembled and oriented, and chromosomes are attached to the spindle.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of spindle checkpoint","termid":"GO:0090231"},{"relation_name":"is_a","term_name":"negative regulation of cell cycle checkpoint","termid":"GO:1901977"},{"relation_name":"negatively_regulates","term_name":"spindle checkpoint signaling","termid":"GO:0031577"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00883":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of spindle checkpoint","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"spindle checkpoint silencing","type":"narrow"}],"termid":"GO:0090233","terms_by_termid":{"GO:0140499":null,"GO:1902426":null}}


id: PBO:0040651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BBSome interacting protein 1","termid":"PBO:0040651"}


id: PBO:0072113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S14 pseudogene 2","termid":"PBO:0072113"}


id: PBO:0090215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase, meiotic, STKc MAK-like Mde3","termid":"PBO:0090215"}


id: FYPO:0001963
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of papulacandin B than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0001985","FYPO:0000139","FYPO:0002682"],"is_obsolete":false,"name":"resistance to papulacandin B","synonyms":[{"name":"resistance to papulacandin B during mitotic cell cycle","type":"related"},{"name":"resistance to papulacandin B during vegetative growth","type":"exact"},{"name":"resistant to papulacandin B","type":"exact"}],"termid":"FYPO:0001963"}


id: PBO:0069398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 658, pseudogene","termid":"PBO:0069398"}


id: MONDO:1011062
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute-onset renal failure from deposition of oxalate crystals in renal tubules that occurs in cats due to a mutation in the GRHPR gene.","definition_xrefs":["OMIA:000821-9685"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"nephropathy, non-human animal","termid":"MONDO:1011907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary hyperoxaluria, GRHPR-related, domestic cat","synonyms":[{"name":"primary hyperoxaluria type II (Oxalosis II), domestic cat","type":"related"}],"termid":"MONDO:1011062","xrefs":{"Monarch":{"xref_id":"1011062"}}}


id: GO:0050022
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-arabinose + NAD+ = L-arabinono-1,4-lactone + NADH.","definition_xrefs":["EC:1.1.1.46","MetaCyc:L-ARABINOSE-1-DEHYDROGENASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"L-arabinose 1-dehydrogenase (NAD+) activity","secondary_identifiers":["RHEA:17925"],"synonyms":[{"name":"L-arabinose 1-dehydrogenase activity","type":"broad"},{"name":"L-arabinose:NAD+ 1-oxidoreductase activity","type":"related"}],"termid":"GO:0050022"}


id: GO:0001705
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of ectoderm during gastrulation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formation of primary germ layer","termid":"GO:0001704"},{"relation_name":"part_of","term_name":"ectoderm development","termid":"GO:0007398"}],"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":"ectoderm formation","termid":"GO:0001705"}


id: PR:Q09921
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1F7.10 gene.","definition_xrefs":["UniProtKB:Q09921","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 C1F7.10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F7.10","synonyms":[{"name":"Spom972h-SPAC1F7.10","type":"exact"}],"termid":"PR:Q09921"}


id: GO:0034609
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Insertion of the male copulatory spicules into the hermaphrodite. Spicule insertion behavior initiates when the male cloaca contacts the vulva. During most mating encounters, the spicule tips will prod the vulva continuously until they partially penetrate, which then causes the protractors to contract completely so that the spicules extend through the vulva.","definition_xrefs":["PMID:18050467"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male mating behavior","termid":"GO:0060179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"spicule insertion","termid":"GO:0034609"}


id: MONDO:0021140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A characteristic of a disease in which the disease is present at birth, regardless of cause.","definition_xrefs":["Wikipedia:Birth_defect"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital or acquired","termid":"MONDO:0021139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital","secondary_identifiers":["icd11.foundation:1048408993"],"synonyms":[{"name":"inborn","type":"exact"}],"termid":"MONDO:0021140","xrefs":{"Monarch":{"xref_id":"0021140"}}}


id: MONDO:0016533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial visceral amyloidosis","termid":"MONDO:0007099"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0021179"],"is_obsolete":false,"name":"apolipoprotein A-II amyloidosis","secondary_identifiers":["Orphanet:238269","GARD:20631","UMLS:C5679845","MEDGEN:1842484"],"synonyms":[{"name":"AApoAII amyloidosis","type":"exact"},{"name":"familial amyloid nephropathy due to apolipoprotein A-II variant","type":"exact"},{"name":"familial renal amyloidosis due to apolipoprotein A-II variant","type":"exact"},{"name":"hereditary amyloid nephropathy due to apolipoprotein A-II variant","type":"exact"},{"name":"hereditary renal amyloidosis due to apolipoprotein A-II variant","type":"exact"}],"termid":"MONDO:0016533","xrefs":{"Monarch":{"xref_id":"0016533"}}}


id: GO:0015880
data:
  {"annotated_genes":["SJAG_03452"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70279],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990559"}]},"cv_name":"biological_process","definition":"The directed movement of coenzyme A into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Coenzyme A, 3'-phosphoadenosine-(5')diphospho(4')pantatheine, is an acyl carrier in many acylation and acyl-transfer reactions in which the intermediate is a thiol ester.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transport","termid":"GO:0015711"},{"relation_name":"is_a","term_name":"organophosphate ester transport","termid":"GO:0015748"},{"relation_name":"is_a","term_name":"nucleobase-containing compound transport","termid":"GO:0015931"},{"relation_name":"is_a","term_name":"amide transport","termid":"GO:0042886"},{"relation_name":"is_a","term_name":"sulfur compound transport","termid":"GO:0072348"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03452":null},"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:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"coenzyme A transport","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0015880","terms_by_termid":{"GO:1990559":null}}


id: PBO:0004702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma tubulin complex subunit Gfh1","termid":"PBO:0004702"}


id: MONDO:0018160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited malignant tumor that originates in the nuclear layer of the retina. A predisposition to retinoblastoma has been associated with 13q14 cytogenetic abnormalities. Patients with the inherited form appear to be at increased risk for secondary nonocular malignancies such as osteosarcoma, malignant fibrous histiocytoma, and fibrosarcoma.","definition_xrefs":["NCIT:C8495"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinoblastoma","termid":"MONDO:0008380"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"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:0005328"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"hereditary retinoblastoma","secondary_identifiers":["Orphanet:357027","GARD:17544","UMLS:C0751483","MEDGEN:155869","DOID:4648","OMIM:180200"],"synonyms":[{"name":"RB1","type":"exact"},{"name":"familial retinoblastoma","type":"exact"},{"name":"hereditary retinoblastoma","type":"exact"},{"name":"retinoblastoma, autosomal dominant, somatic mutation","type":"exact"},{"name":"retinoblastoma, trilateral, autosomal dominant, somatic mutation","type":"exact"}],"termid":"MONDO:0018160","xrefs":{"Monarch":{"xref_id":"0018160"}}}


id: MONDO:0017955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete granulomatous autoinflammatory syndrome (obsolete MONDO:0017955)","secondary_identifiers":["Orphanet:324930"],"termid":"MONDO:0017955","xrefs":{"Monarch":{"xref_id":"0017955"}}}


id: GO:0015370
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: solute(out) + Na+(out) = solute(in) + Na+(in).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium ion transmembrane transporter activity","termid":"GO:0015081"},{"relation_name":"is_a","term_name":"solute:monoatomic cation symporter activity","termid":"GO:0015294"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"solute:sodium symporter activity","secondary_identifiers":["Reactome:R-HSA-8876283"],"synonyms":[{"name":"proline/glycine/betaine:hydrogen/sodium symporter activity","type":"narrow"}],"termid":"GO:0015370"}


id: PBO:0074863
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 49A","termid":"PBO:0074863"}


id: SO:0000286
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence directly repeated at both ends of a defined sequence, of the sort typically found in retroviruses.","direct_ancestors":[{"relation_name":"is_a","term_name":"repeat_region","termid":"SO:0000657"},{"relation_name":"part_of","term_name":"LTR_retrotransposon","termid":"SO:0000186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long_terminal_repeat","secondary_identifiers":["http://en.wikipedia.org/wiki/Long_terminal_repeat"],"synonyms":[{"name":"INSDC_feature:repeat_region","type":"broad"},{"name":"INSDC_qualifier:long_terminal_repeat","type":"exact"},{"name":"LTR","type":"exact"},{"name":"direct terminal repeat","type":"related"},{"name":"long terminal repeat","type":"exact"}],"termid":"SO:0000286"}


id: PBO:0066472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger and FYVE like domain containing E3 ubiquitin protein ligase","termid":"PBO:0066472"}


id: PBO:0034465
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_magnesium","termid":"PBO:0034465"}


id: PR:Q10348
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An endonuclease V that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01577","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":"endonuclease C1F12.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F12.06c","secondary_identifiers":["UniProtKB:Q10348"],"synonyms":[{"name":"Spom972h-ENDOV","type":"exact"}],"termid":"PR:Q10348"}


id: PBO:0071302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 25","termid":"PBO:0071302"}


id: PBO:0070063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 20, pseudogene","termid":"PBO:0070063"}


id: MONDO:0044331
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of transient congenital hypothyroidism that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"gene_count":0,"genotype_count":0,"name":"obsolete genetic transient congenital hypothyroidism (obsolete MONDO:0044331)","secondary_identifiers":["Orphanet:226316"],"synonyms":[{"name":"hereditary transient congenital hypothyroidism","type":"exact"}],"termid":"MONDO:0044331","xrefs":{"Monarch":{"xref_id":"0044331"}}}


id: PBO:0065434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, ATPase 1 pseudogene 7","termid":"PBO:0065434"}


id: PBO:0054095
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 1448","termid":"PBO:0054095"}


id: GO:1990649
data:
  {"annotated_genes":["SJAG_00063"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108050],"is_not":false,"summary":null,"term":"GO:1990649"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1,2,4,5-tetrakisphosphate + H2O = 1D-myo-inositol 1,2,4-trisphosphate + phosphate.","definition_xrefs":["PMID:15316017","GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol tetrakisphosphate phosphatase activity","termid":"GO:0052743"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00063":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"inositol-1,2,4,5-tetrakisphosphate 5-phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990649","terms_by_termid":{"GO:1990649":null}}


id: MONDO:0024414
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cellulitis","termid":"MONDO:0005230"},{"relation_name":"is_a","term_name":"anaerobic bacteria infectious disease","termid":"MONDO:0024389"}],"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":"anaerobic cellulitis","secondary_identifiers":["UMLS:C0241828","SCTID:238401006","MEDGEN:537100","ICD9:041.84","ICD9:682.9"],"synonyms":[{"name":"anaerobic cellulitis","type":"exact"}],"termid":"MONDO:0024414","xrefs":{"Monarch":{"xref_id":"0024414"}}}


id: MONDO:0014809
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary neoplastic syndrome in which the cause of the disease is a mutation in the DDX41 gene.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDX41-related hematologic malignancy predisposition syndrome","secondary_identifiers":["MEDGEN:895780","UMLS:C4225174","Orphanet:488647","OMIM:616871","GARD:17899"],"synonyms":[{"name":"DDX41 hereditary neoplastic syndrome","type":"exact"},{"name":"DDX41-related hematologic malignancy predisposition syndrome","type":"exact"},{"name":"MPLPF","type":"exact"},{"name":"hereditary neoplastic syndrome caused by mutation in DDX41","type":"exact"},{"name":"myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to","type":"exact"},{"name":"susceptibility to familial (multiple types) myeloproliferative/lymphoproliferative neoplasms","type":"related"}],"termid":"MONDO:0014809","xrefs":{"Monarch":{"xref_id":"0014809"}}}


id: PBO:0003697
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sfr1 assembly at DNA damage sites is dependent on Rhp51","termid":"PBO:0003697"}


id: GO:0044206
data:
  {"annotated_genes":["SJAG_00533","SJAG_04354","SJAG_04709","SJAG_03708","SJAG_04713"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67732,87227,88211,91734,92735],"is_not":false,"summary":null,"term":"GO:0044206"}]},"cv_name":"biological_process","definition":"Any process which produces UMP, uridine monophosphate, from derivatives of it (e.g. cytidine, uridine, cytosine) without de novo synthesis.","definition_xrefs":["GOC:ecd","PMID:15096496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UMP biosynthetic process","termid":"GO:0006222"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide salvage","termid":"GO:0010138"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00533":null,"SJAG_03708":null,"SJAG_04354":null,"SJAG_04709":null,"SJAG_04713":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"UMP salvage","references_by_uniquename":{"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"UMP biosynthesis via nucleoside salvage pathway","type":"exact"},{"name":"UMP biosynthetic process via nucleoside salvage pathway","type":"exact"}],"termid":"GO:0044206","terms_by_termid":{"GO:0044206":null}}


id: PBO:0067698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5.8S ribosomal pseudogene 6","termid":"PBO:0067698"}


id: MONDO:0019294
data:
  {"annotated_genes":["SJAG_03199","SJAG_04008","SJAG_03846"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007145"},{"annotations":[85731,85730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024552"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dermis disorder","termid":"MONDO:0021154"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03199":null,"SJAG_03846":null,"SJAG_04008":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"mixed dermis disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5681484","MEDGEN:1842502","Orphanet:79380"],"termid":"MONDO:0019294","terms_by_termid":{"MONDO:0007145":null,"MONDO:0024552":null},"xrefs":{"Monarch":{"xref_id":"0019294"}}}


id: PBO:0042180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin B1 interacting protein 1","termid":"PBO:0042180"}


id: PBO:0066227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBM33 divergent transcript","termid":"PBO:0066227"}


id: GO:0098574
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the lysosomal membrane that faces the cytoplasm.","definition_xrefs":["GOC:dos","GOC:ab"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic side of membrane","termid":"GO:0098562"},{"relation_name":"part_of","term_name":"lysosomal membrane","termid":"GO:0005765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005773"],"is_obsolete":false,"name":"cytoplasmic side of lysosomal membrane","synonyms":[{"name":"external leaflet of lysosomal membrane","type":"exact"},{"name":"external side of lysosomal membrane","type":"exact"}],"termid":"GO:0098574"}


id: GO:1901976
data:
  {"annotated_genes":["SJAG_03327","SJAG_02169","SJAG_04259","SJAG_01297","SJAG_02336","SJAG_01679","SJAG_03353","SJAG_03681","SJAG_01837","SJAG_03126","SJAG_00883","SJAG_02451"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90486,99350,114011,108006,115643,111706,103647,106987,113524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[93960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[113529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905326"},{"annotations":[116417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090267"},{"annotations":[101093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905325"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell cycle checkpoint.","definition_xrefs":["PMID:23028116","GOC:TermGenie","GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle phase transition","termid":"GO:1901987"},{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"cell cycle checkpoint signaling","termid":"GO:0000075"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00883":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03126":null,"SJAG_03327":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0007049","GO:0023052"],"is_obsolete":false,"name":"regulation of cell cycle checkpoint","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:2001047"],"synonyms":[{"name":"regulation of G1/S checkpoint","type":"related"},{"name":"regulation of G1/S transition checkpoint","type":"related"}],"termid":"GO:1901976","terms_by_termid":{"GO:0090267":null,"GO:0140499":null,"GO:1902426":null,"GO:1905325":null,"GO:1905326":null}}


id: PATO:0002349
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's being located toward the base of an organism relative to another entity.","definition_xrefs":["merriam-webster:http://www.merriam-webster.com/dictionary/basal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basal to","termid":"PATO:0002349"}


id: PBO:0040699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 related protein A1","termid":"PBO:0040699"}


id: MONDO:0009840
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":"Partington-Anderson syndrome","secondary_identifiers":["OMIM:260555","MEDGEN:376699","MESH:C536299","UMLS:C1850075","Orphanet:2829"],"synonyms":[{"name":"Partington-Anderson syndrome","type":"exact"}],"termid":"MONDO:0009840","xrefs":{"Monarch":{"xref_id":"0009840"}}}


id: PBO:0060761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 5","termid":"PBO:0060761"}


id: PBO:0002864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apoptosis-inducing factor homolog Aif1 (predicted)","termid":"PBO:0002864"}


id: PBO:0041589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CA3 antisense RNA 1","termid":"PBO:0041589"}


id: GO:0035097
data:
  {"annotated_genes":["SJAG_01540","SJAG_03680","SJAG_02329","SJAG_02119","SJAG_00756","SJAG_07011","SJAG_00341","SJAG_02768","SJAG_03431","SJAG_00769","SJAG_01325","SJAG_00896","SJAG_04574","SJAG_02170"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[96478,113723,110229,94105,117432,118548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043494"},{"annotations":[115446,109095,75370,90472,73674,70973,78276,71585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048188"}]},"cv_name":"cellular_component","definition":"A multimeric complex that is able to catalyze the addition of methyl groups to histone proteins.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase complex","termid":"GO:0034708"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nucleoplasm","termid":"GO:0005654"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00341":null,"SJAG_00756":null,"SJAG_00769":null,"SJAG_00896":null,"SJAG_01325":null,"SJAG_01540":null,"SJAG_02119":null,"SJAG_02170":null,"SJAG_02329":null,"SJAG_02768":null,"SJAG_03431":null,"SJAG_03680":null,"SJAG_04574":null,"SJAG_07011":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0005654","GO:0032991"],"is_obsolete":false,"name":"histone methyltransferase complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0035097","terms_by_termid":{"GO:0043494":null,"GO:0048188":null}}


id: PBO:0046360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endosulfine alpha pseudogene 2","termid":"PBO:0046360"}


id: GO:0009155
data:
  {"annotated_genes":["SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035863"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of purine deoxyribonucleotide, a compound consisting of deoxyribonucleoside (a purine base linked to a deoxyribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide catabolic process","termid":"GO:0006195"},{"relation_name":"is_a","term_name":"purine deoxyribonucleotide metabolic process","termid":"GO:0009151"},{"relation_name":"is_a","term_name":"deoxyribonucleotide catabolic process","termid":"GO:0009264"},{"relation_name":"is_a","term_name":"deoxyribose phosphate catabolic process","termid":"GO:0046386"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04487":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"purine deoxyribonucleotide catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"purine deoxyribonucleotide breakdown","type":"exact"},{"name":"purine deoxyribonucleotide catabolism","type":"exact"},{"name":"purine deoxyribonucleotide degradation","type":"exact"}],"termid":"GO:0009155","terms_by_termid":{"GO:0035863":null}}


id: MONDO:0008778
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":"amyloidosis, cutaneous bullous","secondary_identifiers":["OMIM:204900","ICD9:277.39","MESH:C562644","SCTID:38606009","UMLS:C0268399","MEDGEN:78672"],"synonyms":[{"name":"amyloidosis, cutaneous bullous","type":"exact"}],"termid":"MONDO:0008778","xrefs":{"Monarch":{"xref_id":"0008778"}}}


id: PBO:0066931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 233","termid":"PBO:0066931"}


id: FYPO:0004978
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 a new growing cell tip is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to new cell tip","termid":"FYPO:0004977"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"increased protein localization to new growing cell tip","synonyms":[{"name":"increased protein localisation to new growing cell tip","type":"exact"},{"name":"increased protein localization to new growing cell end","type":"exact"},{"name":"increased protein localization to new growing cell tip during mitotic cell cycle","type":"related"},{"name":"increased protein localization to new growing cell tip during vegetative growth","type":"exact"}],"termid":"FYPO:0004978"}


id: MOD:00899
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to N-palmitoyl-S-diacylglycerol-L-cysteine.","definition_xrefs":["RESID:AA0069#var","RESID:AA0107#var"],"direct_ancestors":[{"relation_name":"has_functional_parent","term_name":"N-palmitoyl-L-cysteine","termid":"MOD:00069"},{"relation_name":"has_functional_parent","term_name":"S-diacylglycerol-L-cysteine","termid":"MOD:00116"},{"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":"N-palmitoyl-S-diacylglycerol-L-cysteine","termid":"MOD:00899"}


id: GO:0016511
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 endothelin-converting enzyme activity (obsolete GO:0016511)","synonyms":[{"name":"endothelin-converting enzyme activity","type":"exact"}],"termid":"GO:0016511"}


id: PBO:0029612
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_tapered_cell","termid":"PBO:0029612"}


id: GO:0033267
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A part of an axon, a cell projection of a neuron.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete axon part (obsolete GO:0033267)","termid":"GO:0033267"}


id: FYPO:0007623
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of mitochondrial respiratory chain complex III assembly is decreased.","definition_xrefs":["GO:0034551","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased mitochondrial respiratory chain complex assembly","termid":"FYPO:0007122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased mitochondrial respiratory chain complex III assembly","synonyms":[{"name":"decreased mitochondrial respiratory chain complex III assembly during mitotic cell cycle","type":"related"},{"name":"decreased mitochondrial respiratory chain complex III assembly during vegetative growth","type":"exact"},{"name":"decreased respiratory chain complex III assembly","type":"exact"}],"termid":"FYPO:0007623"}


id: PBO:0057285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 505","termid":"PBO:0057285"}


id: PBO:0078942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon CCT) 9-1","termid":"PBO:0078942"}


id: GO:0004448
data:
  {"annotated_genes":["SJAG_04362"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73629],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004450"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: isocitrate + NAD(P)+ = 2-oxoglutarate + CO2 + NAD(P)H.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04362":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":"isocitrate dehydrogenase [NAD(P)+] activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"IDH activity","type":"related"},{"name":"IDP activity","type":"related"},{"name":"isocitrate dehydrogenase activity","type":"exact"},{"name":"isocitric acid dehydrogenase activity","type":"exact"},{"name":"isocitric dehydrogenase activity","type":"exact"},{"name":"oxalosuccinate carboxylase activity","type":"exact"},{"name":"oxalosuccinate decarboxylase activity","type":"exact"},{"name":"oxalosuccinic decarboxylase activity","type":"exact"}],"termid":"GO:0004448","terms_by_termid":{"GO:0004450":null}}


id: MONDO:0958128
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bronchiolitis obliterans syndrome","termid":"MONDO:0015265"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-transplant-related bronchiolitis obliterans","secondary_identifiers":["UMLS:C5925142","MEDGEN:1863569","Orphanet:658612"],"termid":"MONDO:0958128","xrefs":{"Monarch":{"xref_id":"0958128"}}}


id: GO:0052407
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism involving carbohydrates within a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete metabolism by organism of carbohydrate in other organism involved in symbiotic interaction (obsolete GO:0052407)","synonyms":[{"name":"metabolism by organism of carbohydrate in other organism during symbiotic interaction","type":"related"}],"termid":"GO:0052407"}


id: GO:0070565
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex of DNA and protein located at the end of a linear chromosome that enables replication of the telomeric repeat sequences at the end of a linear chromosome.","definition_xrefs":["GOC:pde","PMID:19179534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex","termid":"GO:0032993"},{"relation_name":"part_of","term_name":"chromosome, telomeric region","termid":"GO:0000781"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"telomere-telomerase complex","termid":"GO:0070565"}


id: PBO:0086483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative, non-essential component vacuolar ATPase; conserved in fungi; SWAT-GFP fusion protein localizes to vacuole membrane; partially overlaps the dubious genes YPR169W-A, YPR170W-A and YRP170C","termid":"PBO:0086483"}


id: MOD:01617
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to O-(6-phosphomannosyl)-L-threonine.","definition_xrefs":["PubMed:20044576","RESID:AA0514"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-glycosyl-L-threonine","termid":"MOD:00005"},{"relation_name":"is_a","term_name":"mannosylated residue","termid":"MOD:00595"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-(6-phosphomannosyl)-L-threonine","synonyms":[{"name":"(2S,3R)-2-amino-3-[6-phosphonooxy-alpha-D-mannopyranosyloxy]butanoic acid","type":"exact"},{"name":"CARBOHYD O-linked (Man6P) threonine","type":"exact"},{"name":"O-(6-phosphomannosyl)-L-threonine","type":"exact"},{"name":"O3-(6-phosphomannosyl)threonine","type":"exact"}],"termid":"MOD:01617"}


id: PBO:0090250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone lysine methyltransferase Set5","termid":"PBO:0090250"}


id: FYPO:0007677
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A localization phenotype observed in the vegetative growth phase of the life cycle in which the distribution of sterols in cellular membranes is abnormal.","definition_xrefs":["PMID:32320462","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal membrane lipid distribution","termid":"FYPO:0006545"}],"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"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal sterol distribution","termid":"FYPO:0007677"}


id: PBO:0055322
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 2750","termid":"PBO:0055322"}


id: GO:0072261
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of extraglomerular glomerular mesangium cells in the metanephros by cell division, resulting in the expansion of their population. Extraglomerular mesangial cells (also known as lacis cells, Goormaghtigh cells) are light-staining cells in the kidney found outside the glomerulus, near the vascular pole and macula densa.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extraglomerular mesangial cell proliferation","termid":"GO:0072122"},{"relation_name":"is_a","term_name":"cell proliferation involved in metanephros development","termid":"GO:0072203"},{"relation_name":"part_of","term_name":"metanephric nephron development","termid":"GO:0072210"}],"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":"metanephric extraglomerular mesangial cell proliferation involved in metanephros development","synonyms":[{"name":"metanephric Goormaghtigh proliferation","type":"related"},{"name":"metanephric lacis cell proliferation","type":"related"}],"termid":"GO:0072261"}


id: MONDO:0003830
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chromophil adenoma of the kidney","termid":"MONDO:0003829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"type 1 papillary adenoma of the kidney","secondary_identifiers":["UMLS:C1519706","MEDGEN:276906","DOID:6258","NCIT:C39809"],"synonyms":[{"name":"type 1 papillary adenoma of the kidney","type":"exact"},{"name":"type 1 renal papillary adenoma","type":"exact"}],"termid":"MONDO:0003830","xrefs":{"Monarch":{"xref_id":"0003830"}}}


id: FYPO:0006444
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A conjugation phenotype in which regulation of transcription in response to starvation for one or more amino acids is abnormal.","definition_xrefs":["PMID:29432178","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to starvation during vegetative growth","termid":"FYPO:0001339"},{"relation_name":"is_a","term_name":"abnormal regulation of transcription during vegetative growth","termid":"FYPO:0004527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0001985","FYPO:0006551","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal transcriptional response to amino acid starvation","synonyms":[{"name":"abnormal regulation of transcription from RNA polymerase II promoter in response to amino acid starvation","type":"exact"}],"termid":"FYPO:0006444"}


id: MONDO:0006309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A variant of gastric adenocarcinoma with more than half of the tumor containing extracellular mucinous pools.","definition_xrefs":["NCIT:C5248"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diffuse gastric adenocarcinoma","termid":"MONDO:0005017"},{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"},{"relation_name":"is_a","term_name":"gastric adenocarcinoma","termid":"MONDO:0005036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"mucinous gastric adenocarcinoma","secondary_identifiers":["MEDGEN:235338","DOID:3716","ONCOTREE:MSTAD","UMLS:C1334809","EFO:1000386"],"synonyms":[{"name":"MSTAD","type":"related"},{"name":"mucinous adenocarcinoma of stomach","type":"exact"},{"name":"mucinous adenocarcinoma of the stomach","type":"exact"},{"name":"mucinous gastric adenocarcinoma","type":"exact"},{"name":"mucinous stomach adenocarcinoma","type":"exact"},{"name":"stomach mucinous adenocarcinoma","type":"exact"}],"termid":"MONDO:0006309","xrefs":{"Monarch":{"xref_id":"0006309"}}}


id: PBO:0068252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 28S ribosomal N4","termid":"PBO:0068252"}


id: PBO:0058469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5571","termid":"PBO:0058469"}


id: GO:0050849
data:
  {"annotated_genes":["SJAG_03799","SJAG_02858"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115870,100751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106057"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of calcium-mediated signaling.","definition_xrefs":["GOC:ai","PMID:11696592"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of calcium-mediated signaling","termid":"GO:0050848"},{"relation_name":"is_a","term_name":"negative regulation of intracellular signal transduction","termid":"GO:1902532"},{"relation_name":"negatively_regulates","term_name":"calcium-mediated signaling","termid":"GO:0019722"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02858":null,"SJAG_03799":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of calcium-mediated signaling","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of calcium-mediated signaling","type":"exact"},{"name":"down-regulation of calcium-mediated signaling","type":"exact"},{"name":"downregulation of calcium-mediated signaling","type":"exact"},{"name":"inhibition of calcium-mediated signaling","type":"narrow"},{"name":"negative regulation of calcium-mediated signalling","type":"exact"}],"termid":"GO:0050849","terms_by_termid":{"GO:0106057":null}}


id: PBO:0027786
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_serine_phosphorylation_during_nitrogen_starvation","termid":"PBO:0027786"}


id: MONDO:0018988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Iridocorneal endothelial (ICE) syndrome describes a group of progressive corneal proliferative endotheliopathies comprised of Chandler syndrome, Cogan-Reese syndrome and essential iris atrophy, affecting mainly young adult females and characterized by iris holes and atrophy, papillary distortion, anterior synechiae, corneal edema and often with secondary glaucoma and corneal decompensation as complications","definition_xrefs":["Orphanet:64734"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"obsolete rare acquired eye disease (obsolete MONDO:0015120)","termid":"MONDO:0015120"},{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glaucoma due to a proliferation and differentiation anomaly (obsolete MONDO:0020221)","termid":"MONDO:0020221"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iridocorneal endothelial syndrome","secondary_identifiers":["NCIT:C84792","UMLS:C1096100","MEDGEN:242751","MESH:D057129","MedDRA:10053678","SCTID:129623003","icd11.foundation:265074385","GARD:60"],"synonyms":[{"name":"ICE syndrome","type":"exact"}],"termid":"MONDO:0018988","xrefs":{"Monarch":{"xref_id":"0018988"}}}


id: PBO:0078790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (GTT) 13-1","termid":"PBO:0078790"}


id: GO:0072222
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the metanephric early distal convoluted tubule over time, from its formation to the mature structure. The metanephric early distal convoluted tubule contains metanephric DCT cells and is vasopressin-insensitive.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early distal convoluted tubule development","termid":"GO:0072067"},{"relation_name":"is_a","term_name":"metanephric nephron epithelium development","termid":"GO:0072243"},{"relation_name":"part_of","term_name":"metanephric distal convoluted tubule development","termid":"GO:0072221"}],"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":"metanephric early distal convoluted tubule development","termid":"GO:0072222"}


id: PBO:0026875
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_meiotic_DNA_double-strand_break_clipping","termid":"PBO:0026875"}


id: PBO:0077313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 51","termid":"PBO:0077313"}


id: PBO:0041777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calpain small subunit 1","termid":"PBO:0041777"}


id: GO:0090668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of an endothelial cell in response to the presence of vascular endothelial growth factor (VEGF).","definition_xrefs":["GOC:BHF_miRNA","PMID:21885851","GOC:BHF","GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell chemotaxis to vascular endothelial growth factor","termid":"GO:0090667"}],"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":"endothelial cell chemotaxis to vascular endothelial growth factor","termid":"GO:0090668"}


id: MOD:00273
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts four L-cysteine residues, two L-glutamic acid residues, an L-histidine residue and a four-iron three-sulfur three-oxygen cluster to tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino tetrairon disulfide trioxide.","definition_xrefs":["RESID:AA0268","PubMed:12764602"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron-sulfur cluster containing modification","termid":"MOD:00739"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-cysteine residue","termid":"MOD:02067"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-glutamic acid residue","termid":"MOD:02068"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-histidine residue","termid":"MOD:02070"}],"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":"tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino tetrairon disulfide trioxide","synonyms":[{"name":"4Fe-2S-3O cluster","type":"exact"},{"name":"METAL Iron-oxo-sulfur (4Fe-2O-2S)","type":"exact"},{"name":"METAL Iron-oxo-sulfur (4Fe-2O-2S); via persulfide group","type":"exact"},{"name":"METAL Iron-oxo-sulfur (4Fe-2O-2S); via tele nitrogen","type":"exact"},{"name":"hybrid four iron cluster 2","type":"exact"},{"name":"mu-1:2kappaO-oxido-mu-1:3kappaO-oxido-mu-2:4kappaO-oxido-mu-3:4kappaS-sulfido-mu3-2:3:4kappaS-sulfido-S-cysteinyl-N1'-histidino-O5-glutamato 1-iron-S5-cysteine persulfido-O5-glutamato 2-iron-3,4-bis-(S-cysteinyl iron)","type":"exact"},{"name":"prismane iron-sulfur cofactor","type":"related"},{"name":"tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino tetrairon disulfide trioxide","type":"exact"}],"termid":"MOD:00273"}


id: GO:1905205
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of connective tissue replacement.","definition_xrefs":["GOC:BHF_miRNA","GOC:BHF","GOC:bc","GOC:TermGenie","GO_REF:0000058","PMID:25590961"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of tissue remodeling","termid":"GO:0034105"},{"relation_name":"is_a","term_name":"regulation of connective tissue replacement","termid":"GO:1905203"},{"relation_name":"positively_regulates","term_name":"connective tissue replacement","termid":"GO:0097709"}],"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 connective tissue replacement","synonyms":[{"name":"activation of connective tissue replacement","type":"narrow"},{"name":"up regulation of connective tissue replacement","type":"exact"},{"name":"up-regulation of connective tissue replacement","type":"exact"},{"name":"upregulation of connective tissue replacement","type":"exact"}],"termid":"GO:1905205"}


id: GO:0006840
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of alpha-ketoglutarate and malate into, out of or within a mitochondrion.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial alpha-ketoglutarate/malate transport (obsolete GO:0006840)","synonyms":[{"name":"mitochondrial alpha-ketoglutarate/malate transport","type":"exact"},{"name":"mitochondrial oxoglutarate/malate transport","type":"exact"}],"termid":"GO:0006840"}


id: MONDO:0005338
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chronic outflow obstruction of the eye's drainage canals that can lead to increased internal eye pressure and optic nerve damage.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glaucoma","termid":"MONDO:0005041"}],"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":"open-angle glaucoma","secondary_identifiers":["ICD9:365.13","NCIT:C34641","EFO:0004190","DOID:1067","SCTID:46168003","ICD9:365.1","ICD9:365.10","MEDGEN:6611","MESH:D005902","UMLS:C0017612","SCTID:84494001"],"synonyms":[{"name":"POAG","type":"exact"},{"name":"glaucoma simplex","type":"exact"},{"name":"glaucoma, primary open angle","type":"exact"},{"name":"open angle glaucoma","type":"exact"},{"name":"pigmentary glaucoma","type":"exact"},{"name":"primary open angle glaucoma","type":"exact"},{"name":"wide-angle glaucoma","type":"exact"}],"termid":"MONDO:0005338","xrefs":{"Monarch":{"xref_id":"0005338"}}}


id: PBO:0085632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in G2/M phase progression and response to DNA damage; interacts with Rad53p; contains an RNA recognition motif, a nuclear localization signal, and several SQ/TQ cluster domains; hyperphosphorylated in response to DNA damage","termid":"PBO:0085632"}


id: MONDO:0002574
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm of the prostate. It is characterized by the presence of skeletal muscle exhibiting embryonic features.","definition_xrefs":["NCIT:C5525"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostate rhabdomyosarcoma","termid":"MONDO:0006389"},{"relation_name":"is_a","term_name":"embryonal rhabdomyosarcoma","termid":"MONDO:0009993"},{"relation_name":"is_a","term_name":"prostate cancer, hereditary","termid":"MONDO:0700275"}],"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":"prostate embryonal rhabdomyosarcoma","secondary_identifiers":["DOID:3251","MEDGEN:233873","UMLS:C1335508"],"synonyms":[{"name":"embryonal rhabdomyosarcoma (disease) of prostate gland","type":"exact"},{"name":"embryonal rhabdomyosarcoma of prostate","type":"exact"},{"name":"embryonal rhabdomyosarcoma of the prostate","type":"exact"},{"name":"prostate embryonal rhabdomyosarcoma","type":"exact"},{"name":"prostate gland embryonal rhabdomyosarcoma (disease)","type":"exact"}],"termid":"MONDO:0002574","xrefs":{"Monarch":{"xref_id":"0002574"}}}


id: PBO:0005409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Cwf5","termid":"PBO:0005409"}


id: PBO:0055630
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 3069","termid":"PBO:0055630"}


id: FYPO:0005545
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 nuclear chromatin organization is abnormal, such that regions containing transposons (Tf2 elements) are physically clustered to a lower extent than normal.","definition_xrefs":["PomBase:mah","PMID:27343236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin organization during vegetative growth","termid":"FYPO:0001352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000641"],"is_obsolete":false,"name":"decreased Tf body formation","synonyms":[{"name":"decreased Tf body formation during mitotic cell cycle","type":"related"},{"name":"decreased Tf body formation during vegetative growth","type":"exact"},{"name":"decreased Tf clustering","type":"exact"},{"name":"decreased Tf2 body formation","type":"exact"},{"name":"decreased clustering of Tf2 bodies","type":"exact"},{"name":"reduced Tf body formation","type":"exact"}],"termid":"FYPO:0005545"}


id: PBO:0036151
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H2A_phosphorylation_at_G4_motif_during_vegetative_growth","termid":"PBO:0036151"}


id: GO:0006850
data:
  {"annotated_genes":["SJAG_01924","SJAG_04593"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62889,76737],"is_not":false,"summary":null,"term":"GO:0006850"}]},"cv_name":"biological_process","definition":"The process in which pyruvate is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:22628558","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate transmembrane transport","termid":"GO:1901475"},{"relation_name":"is_a","term_name":"mitochondrial transmembrane transport","termid":"GO:1990542"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01924":null,"SJAG_04593":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"mitochondrial pyruvate transmembrane transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"secondary_identifiers":["GO:1902361"],"synonyms":[{"name":"mitochondrial pyruvate transport","type":"related"},{"name":"pyruvate membrane transport in mitochondria","type":"related"},{"name":"pyruvate membrane transport in mitochondrion","type":"related"},{"name":"pyruvate transmembrane transport in mitochondria","type":"related"},{"name":"pyruvate transmembrane transport in mitochondrion","type":"related"}],"termid":"GO:0006850","terms_by_termid":{"GO:0006850":null}}


id: PATO:0001778
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A strength which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"strength","termid":"PATO:0001230"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased strength","synonyms":[{"name":"high strength","type":"exact"}],"termid":"PATO:0001778"}


id: GO:0061216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter that contributes to the mesonephros progressing from its initial formation to the mature state.","definition_xrefs":["GOC:mtg_kidney_jan10"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in mesonephros development (obsolete GO:0061216)","termid":"GO:0061216"}


id: MONDO:0001990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare malignant peripheral nerve sheath tumor that arises from the heart.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart sarcoma","termid":"MONDO:0003354"},{"relation_name":"is_a","term_name":"malignant peripheral nerve sheath tumor","termid":"MONDO:0017827"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005267"],"is_obsolete":false,"name":"malignant cardiac peripheral nerve sheath neoplasm","secondary_identifiers":["UMLS:C1334569","MEDGEN:233146","DOID:14534","NCIT:C5367"],"synonyms":[{"name":"CARDIAC schwannoma, malignant","type":"exact"},{"name":"Cardiac MPNST","type":"exact"},{"name":"Cardiac malignant peripheral nerve sheath tumor","type":"exact"},{"name":"Cardiac malignant peripheral nerve sheath tumour","type":"exact"},{"name":"MPNST of heart","type":"exact"},{"name":"MPNST of the heart","type":"exact"},{"name":"heart MPNST","type":"exact"},{"name":"heart malignant peripheral nerve sheath tumor","type":"exact"},{"name":"heart malignant peripheral nerve sheath tumour","type":"exact"},{"name":"malignant Cardiac neurilemmoma","type":"exact"},{"name":"malignant Cardiac peripheral nerve sheath neoplasm","type":"exact"},{"name":"malignant Cardiac peripheral nerve sheath tumor","type":"exact"},{"name":"malignant Cardiac peripheral nerve sheath tumour","type":"exact"},{"name":"malignant Cardiac schwannoma","type":"exact"},{"name":"malignant heart neurilemmoma","type":"exact"},{"name":"malignant heart peripheral nerve sheath neoplasm","type":"exact"},{"name":"malignant heart peripheral nerve sheath tumor","type":"exact"},{"name":"malignant heart peripheral nerve sheath tumour","type":"exact"},{"name":"malignant heart schwannoma","type":"exact"},{"name":"malignant neurilemmoma of heart","type":"exact"},{"name":"malignant neurilemmoma of the heart","type":"exact"},{"name":"malignant peripheral nerve sheath neoplasm of heart","type":"exact"},{"name":"malignant peripheral nerve sheath neoplasm of the heart","type":"exact"},{"name":"malignant peripheral nerve sheath tumor of heart","type":"exact"},{"name":"malignant peripheral nerve sheath tumor of the heart","type":"exact"},{"name":"malignant peripheral nerve sheath tumour of heart","type":"exact"},{"name":"malignant peripheral nerve sheath tumour of the heart","type":"exact"},{"name":"malignant schwannoma of heart","type":"exact"},{"name":"malignant schwannoma of the heart","type":"exact"}],"termid":"MONDO:0001990","xrefs":{"Monarch":{"xref_id":"0001990"}}}


id: PBO:0072995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCML2 pseudogene 2","termid":"PBO:0072995"}


id: PBO:0059627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MTCH1 pseudogene 2","termid":"PBO:0059627"}


id: MONDO:0000814
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute B-lymphoblastic leukemia occurring in adults.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult acute lymphoblastic leukemia","termid":"MONDO:0003541"},{"relation_name":"is_a","term_name":"precursor B-cell acute lymphoblastic leukemia","termid":"MONDO:0020511"}],"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:0005046","MONDO:0005570"],"is_obsolete":false,"name":"B-cell adult acute lymphocytic leukemia","secondary_identifiers":["UMLS:C0279593","EFO:1001935","NCIT:C9143","MEDGEN:79010","DOID:0060592"],"synonyms":[{"name":"B acute lymphoblastic leukaemia","type":"broad"},{"name":"B acute lymphoblastic leukemia","type":"broad"},{"name":"B cell adult ALL","type":"exact"},{"name":"B cell adult acute lymphoblastic leukaemia","type":"exact"},{"name":"B cell adult acute lymphoblastic leukemia","type":"exact"},{"name":"B cell adult acute lymphocytic leukaemia","type":"exact"},{"name":"B cell adult acute lymphocytic leukemia","type":"exact"},{"name":"B-cell adult ALL","type":"exact"},{"name":"B-cell adult acute lymphoblastic leukaemia","type":"exact"},{"name":"B-cell adult acute lymphoblastic leukemia","type":"exact"},{"name":"B-cell childhood acute lymphoblastic leukaemia of adults","type":"exact"},{"name":"B-cell childhood acute lymphoblastic leukemia of adults","type":"exact"},{"name":"adult B acute lymphoblastic leukaemia","type":"exact"},{"name":"adult B acute lymphoblastic leukemia","type":"exact"},{"name":"adult B cell ALL","type":"exact"},{"name":"adult B cell acute lymphoblastic leukaemia","type":"exact"},{"name":"adult B cell acute lymphoblastic leukemia","type":"exact"},{"name":"adult B cell acute lymphocytic leukaemia","type":"exact"},{"name":"adult B cell acute lymphocytic leukemia","type":"exact"},{"name":"adult B-cell ALL","type":"exact"},{"name":"adult B-cell acute lymphoblastic leukaemia","type":"exact"},{"name":"adult B-cell acute lymphoblastic leukemia","type":"exact"},{"name":"adult B-cell acute lymphocytic leukaemia","type":"exact"},{"name":"adult B-cell acute lymphocytic leukemia","type":"exact"},{"name":"adult B-cell childhood acute lymphoblastic leukaemia","type":"exact"},{"name":"adult B-cell childhood acute lymphoblastic leukemia","type":"exact"},{"name":"adult B-cell lymphocytic leukaemia","type":"exact"},{"name":"adult B-cell lymphocytic leukemia","type":"exact"},{"name":"adult B-lymphoblastic leukaemia","type":"exact"},{"name":"adult B-lymphoblastic leukemia","type":"exact"},{"name":"adult precursor B-lymphoblastic leukaemia","type":"exact"},{"name":"adult precursor B-lymphoblastic leukemia","type":"exact"}],"termid":"MONDO:0000814","xrefs":{"Monarch":{"xref_id":"0000814"}}}


id: PBO:0060721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A9","termid":"PBO:0060721"}


id: PBO:0054372
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 1766","termid":"PBO:0054372"}


id: GO:0061463
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction O-acetyl-ADP-ribose + H2O = ADP-ribose + acetate. Removes the acetyl group from either the 2'' or 3'' position of O-acetyl-ADP-ribose.","definition_xrefs":["EC:3.1.1.106"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deacetylase activity","termid":"GO:0019213"},{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0019213"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0003674","GO:0019213","GO:0016787"],"is_obsolete":false,"name":"O-acetyl-ADP-ribose deacetylase activity","termid":"GO:0061463"}


id: MOD:00086
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-palmitoyl-L-lysine.","definition_xrefs":["RESID:AA0077","OMSSA:93","PubMed:2498336","PubMed:7801126","Unimod:47#K","PubMed:7939682"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-palmitoylated residue","termid":"MOD:00651"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"},{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01875","MOD:01155"],"is_obsolete":false,"name":"N6-palmitoyl-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-(hexadecanoylamino)hexanoic acid","type":"exact"},{"name":"2-amino-6-(hexadecanamido)hexanoic acid","type":"exact"},{"name":"LIPID N6-palmitoyl lysine","type":"exact"},{"name":"N(zeta)-palmitoyllysine","type":"exact"},{"name":"N6-(1-oxohexadecyl)-L-lysine","type":"exact"},{"name":"N6-hexadecanoylated L-lysine","type":"exact"},{"name":"N6-palmitoyl-L-lysine","type":"exact"},{"name":"N6-palmitoylated L-lysine","type":"exact"},{"name":"N6PamLys","type":"exact"},{"name":"Palmitoyl","type":"related"},{"name":"Palmitoylation","type":"related"},{"name":"epsilon-palmitoyllysine","type":"exact"},{"name":"palmitoylationk","type":"exact"}],"termid":"MOD:00086"}


id: PBO:0045757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endothelin converting enzyme like 1 pseudogene 1","termid":"PBO:0045757"}


id: PBO:0060783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B10 pseudogene 1","termid":"PBO:0060783"}


id: PBO:0077329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 65","termid":"PBO:0077329"}


id: MONDO:0015532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-Langerhans cell histiocytosis","termid":"MONDO:0015531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"generalized eruptive histiocytosis","secondary_identifiers":["SCTID:110980006","MEDGEN:578001","Orphanet:157991","UMLS:C0347404","GARD:20018"],"synonyms":[{"name":"generalised eruptive histiocytoma","type":"exact"},{"name":"generalized eruptive histiocytoma","type":"exact"}],"termid":"MONDO:0015532","xrefs":{"Monarch":{"xref_id":"0015532"}}}


id: PR:Q76PC3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mme1 gene.","definition_xrefs":["UniProtKB:Q76PC3","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 mitochondrial carrier C1442.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1442.03","synonyms":[{"name":"Spom972h-mme1","type":"exact"}],"termid":"PR:Q76PC3"}


id: PR:O43022
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rsn1 gene.","definition_xrefs":["UniProtKB:O43022","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 C354.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC354.08c","synonyms":[{"name":"Spom972h-rsn1","type":"exact"}],"termid":"PR:O43022"}


id: GO:0050299
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + streptomycin = ADP + 2 H+ + streptomycin 3''-phosphate.","definition_xrefs":["RHEA:18377","EC:2.7.1.87"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoglycoside phosphotransferase activity","termid":"GO:0034071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016301","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"streptomycin 3''-kinase activity","secondary_identifiers":["KEGG_REACTION:R02227","MetaCyc:STREPTOMYCIN-3-KINASE-RXN"],"synonyms":[{"name":"ATP:streptomycin 3''-phosphotransferase activity","type":"related"},{"name":"streptomycin 3''-kinase (phosphorylating)","type":"related"},{"name":"streptomycin 3''-phosphotransferase activity","type":"related"}],"termid":"GO:0050299"}


id: PBO:0045104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deleted in malignant brain tumors 1","termid":"PBO:0045104"}


id: GO:0060445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the branching structure of the salivary gland is generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of a branching epithelium","termid":"GO:0061138"},{"relation_name":"part_of","term_name":"salivary gland morphogenesis","termid":"GO:0007435"}],"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":"branching involved in salivary gland morphogenesis","termid":"GO:0060445"}


id: GO:0030544
data:
  {"annotated_genes":["SJAG_00436","SJAG_00403","SJAG_03094","SJAG_03135","SJAG_01914","SJAG_01160","SJAG_03955"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58994,66376,66607,70737,77602,79538,79777],"is_not":false,"summary":null,"term":"GO:0030544"}]},"cv_name":"molecular_function","definition":"Binding to a Hsp70 protein, heat shock proteins around 70kDa in size.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heat shock protein binding","termid":"GO:0031072"},{"relation_name":"is_a","term_name":"protein-folding chaperone binding","termid":"GO:0051087"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00403":null,"SJAG_00436":null,"SJAG_01160":null,"SJAG_01914":null,"SJAG_03094":null,"SJAG_03135":null,"SJAG_03955":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"Hsp70 protein binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"termid":"GO:0030544","terms_by_termid":{"GO:0030544":null}}


id: PBO:0062029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily R member 1, pseudogene","termid":"PBO:0062029"}


id: MONDO:0016825
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mitochondrial myopathy-lactic acidosis-deafness is a type of metabolic myopathy described only in two sisters to date, presenting during childhood, and characterized clinically by growth failure, severe muscle weakness, and moderate sensorineural deafness and biochemically by metabolic acidosis, elevated serum pyruvate concentration, hyperalaninemia and hyperalaninuria. There have been no further descriptions in the literature since 1973.","definition_xrefs":["Orphanet:2597"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial myopathy","termid":"MONDO:0009637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066","MONDO:0005336"],"is_obsolete":false,"name":"mitochondrial myopathy-lactic acidosis-deafness syndrome","secondary_identifiers":["UMLS:C1855033","GARD:3682","OMIM:251950","MESH:C537476","MEDGEN:343245"],"synonyms":[{"name":"MMLA","type":"related"},{"name":"metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness","type":"related"},{"name":"mitochondrial myopathy with lactic acidosis","type":"exact"},{"name":"mitochondrial myopathy-lactic acidosis-hearing loss syndrome","type":"exact"}],"termid":"MONDO:0016825","xrefs":{"Monarch":{"xref_id":"0016825"}}}


id: PBO:0086596
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; expression induced in cells treated with mycotoxins patulin or citrinin; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0086596"}


id: PR:B5BP46
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC460.02c gene.","definition_xrefs":["UniProtKB:B5BP46","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":"glutathione S-transferase C460.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC460.02c","synonyms":[{"name":"Spom972h-SPBC460.02c","type":"exact"},{"name":"glutathione S-transferase C1183.02 (Schizosaccharomyces pombe 972h-)","type":"related"}],"termid":"PR:B5BP46"}


id: PBO:0028771
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_plumbagin","termid":"PBO:0028771"}


id: MONDO:0007615
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Laurin-Sandrow syndrome (LSS) is characterized by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported, and may represent the same entity. The etiology of LSS is unknown. Different modes of inheritance have been suggested.","definition_xrefs":["Orphanet:2378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laurin-Sandrow syndrome","secondary_identifiers":["SCTID:715440003","UMLS:C1851100","OMIM:135750","icd11.foundation:671594481","MEDGEN:340697","DOID:0111350","MESH:C535689","GARD:155"],"synonyms":[{"name":"LSS","type":"related"},{"name":"Sandrow syndrome","type":"exact"},{"name":"fibula and ulna, Duplication of, with absence of tibia and radius","type":"related"},{"name":"fibula ulna duplication tibia radius absence","type":"related"},{"name":"laurin Sandrow syndrome","type":"related"},{"name":"laurin-Sandrow syndrome","type":"exact"},{"name":"laurin-Sandrow syndrome, segmental","type":"related"},{"name":"mirror hands and feet with nasal defects","type":"related"},{"name":"mirror hands and feets-nasal defects syndrome","type":"exact"},{"name":"mirror-Image polydactyly","type":"related"},{"name":"tetramelic mirror-Image polydactyly","type":"related"}],"termid":"MONDO:0007615","xrefs":{"Monarch":{"xref_id":"0007615"}}}


id: PBO:0070972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18 pseudogene 10","termid":"PBO:0070972"}


id: MONDO:0002355
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the glottis.","direct_ancestors":[{"relation_name":"is_a","term_name":"glottis cancer","termid":"MONDO:0002351"},{"relation_name":"is_a","term_name":"laryngeal carcinoma","termid":"MONDO:0002358"}],"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":"glottis carcinoma","secondary_identifiers":["UMLS:C0740083","SCTID:372103002","NCIT:C4923","DOID:2599","MEDGEN:152820"],"synonyms":[{"name":"cancer of glottis","type":"broad"},{"name":"cancer of the glottis","type":"broad"},{"name":"carcinoma of glottis","type":"exact"},{"name":"carcinoma of the glottis","type":"exact"},{"name":"glottic carcinoma","type":"exact"},{"name":"glottic throat cancer","type":"broad"},{"name":"glottis cancer","type":"broad"},{"name":"glottis carcinoma","type":"exact"}],"termid":"MONDO:0002355","xrefs":{"Monarch":{"xref_id":"0002355"}}}


id: MONDO:0012882
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 9","secondary_identifiers":["MESH:C567531","MEDGEN:398108","OMIM:612372","UMLS:C2700440"],"synonyms":[{"name":"MAFD9","type":"exact"},{"name":"MAJOR affective disorder 9","type":"related"},{"name":"bipolar affective disorder","type":"related"},{"name":"major affective disorder 9","type":"exact"},{"name":"major affective disorder-9, susceptibility to","type":"exact"}],"termid":"MONDO:0012882","xrefs":{"Monarch":{"xref_id":"0012882"}}}


id: PBO:0044950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrofolate reductase pseudogene 6","termid":"PBO:0044950"}


id: SO:0001423
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A read produced by the dye terminator method of sequencing.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"read","termid":"SO:0000150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dye_terminator_read","synonyms":[{"name":"dye terminator read","type":"related"}],"termid":"SO:0001423"}


id: PBO:0039943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AT-rich interaction domain 3C","termid":"PBO:0039943"}


id: GO:0060747
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A parental behavior in which fertilized eggs are taken into the mouth and held until hatching.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parental behavior","termid":"GO:0060746"}],"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":"oral incubation","termid":"GO:0060747"}


id: PBO:0051408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 1-40","termid":"PBO:0051408"}


id: GO:0050265
data:
  {"annotated_genes":["SJAG_02370","SJAG_02383"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79513,79553],"is_not":false,"summary":null,"term":"GO:0050265"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: UTP + RNA(n) = diphosphate + RNA(n+1).","definition_xrefs":["EC:2.7.7.52","MetaCyc:RNA-URIDYLYLTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uridylyltransferase activity","termid":"GO:0070569"},{"relation_name":"is_a","term_name":"catalytic activity, acting on RNA","termid":"GO:0140098"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02370":null,"SJAG_02383":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016779","GO:0003674","GO:0003824","GO:0016740","GO:0140098"],"is_obsolete":false,"name":"RNA uridylyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-8941312","RHEA:14785"],"synonyms":[{"name":"TUT activity","type":"related"},{"name":"UTP:RNA uridylyltransferase activity","type":"exact"},{"name":"poly(U) polymerase activity","type":"exact"},{"name":"polynucleotide uridylyltransferase activity","type":"exact"},{"name":"terminal uridylyltransferase activity","type":"related"}],"termid":"GO:0050265","terms_by_termid":{"GO:0050265":null}}


id: PBO:0089252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA queuosine modification protein Qtr3","termid":"PBO:0089252"}


id: PBO:0030586
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_isoleucine_level","termid":"PBO:0030586"}


id: PATO:0001714
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A diameter which is relatively large.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"increased length","termid":"PATO:0000573"},{"relation_name":"is_a","term_name":"diameter","termid":"PATO:0001334"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased diameter","termid":"PATO:0001714"}


id: MOD:01785
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to O-(L-isoglutamyl)-L-threonine, using free L-glutamine and releasing ammonia.","definition_xrefs":["PubMed:8706862","RESID:AA0536#THR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acylated residue","termid":"MOD:00671"},{"relation_name":"is_a","term_name":"O-(L-isoglutamyl)-L-threonine","termid":"MOD:01979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-(L-isoglutamyl)-L-threonine (active site intermediate)","synonyms":[{"name":"(2S)-2-amino-5-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-5-oxopentanoic acid","type":"exact"},{"name":"(2S,3R)-2-amino-3-([(4S)-4-amino-4-carboxybutanoyl]oxy)-propanoic acid","type":"exact"},{"name":"5-(threon-O3-yl)glutamate","type":"exact"},{"name":"O(beta)-(gamma-glutamyl)threonine","type":"exact"},{"name":"O-(L-isoglutamyl)-L-threonine","type":"exact"},{"name":"O3-(isoglutamyl)threonine","type":"exact"}],"termid":"MOD:01785"}


id: GO:1903218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of malate dehydrogenase (decarboxylating) (NADP+) activity.","definition_xrefs":["GOC:TermGenie","PMID:12398416","GOC:sart","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of malate dehydrogenase (decarboxylating) (NADP+) activity (obsolete GO:1903218)","synonyms":[{"name":"regulation of 'malic' enzyme","type":"related"},{"name":"regulation of (S)-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating)","type":"exact"},{"name":"regulation of L-malate:NADP oxidoreductase activity","type":"exact"},{"name":"regulation of NADP-linked decarboxylating malic enzyme","type":"related"},{"name":"regulation of NADP-malic enzyme activity","type":"exact"},{"name":"regulation of NADP-specific malate dehydrogenase activity","type":"exact"},{"name":"regulation of NADP-specific malic enzyme","type":"related"},{"name":"regulation of malate dehydrogenase (NADP, decarboxylating)","type":"exact"},{"name":"regulation of malate dehydrogenase (decarboxylating, NADP)","type":"exact"}],"termid":"GO:1903218"}


id: GO:0071034
data:
  {"annotated_genes":["SJAG_04360","SJAG_03984","SJAG_01064","SJAG_02622","SJAG_00701","SJAG_01521","SJAG_03939","SJAG_01830","SJAG_03745","SJAG_04321"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74874,77314],"is_not":false,"summary":null,"term":"GO:0071034"},{"annotations":[70023,99532,70473,111603,115118,102742,112501,117857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071039"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of cryptic unstable transcripts (CUTs).","definition_xrefs":["GOC:krc","GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CUT metabolic process","termid":"GO:0071043"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00701":null,"SJAG_01064":null,"SJAG_01521":null,"SJAG_01830":null,"SJAG_02622":null,"SJAG_03745":null,"SJAG_03939":null,"SJAG_03984":null,"SJAG_04321":null,"SJAG_04360":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"CUT catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"cryptic unstable transcript catabolic process","type":"exact"}],"termid":"GO:0071034","terms_by_termid":{"GO:0071034":null,"GO:0071039":null}}


id: FYPO:0006104
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of retrotransposon integration is decreased.","definition_xrefs":["PMID:26358720","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transposition","termid":"FYPO:0000591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased retrotransposon integration","synonyms":[{"name":"decreased retrotransposon integration during mitotic cell cycle","type":"related"},{"name":"decreased retrotransposon integration during vegetative growth","type":"exact"},{"name":"decreased transposon integration involved in RNA-mediated transposition","type":"exact"},{"name":"reduced retrotransposon integration","type":"exact"}],"termid":"FYPO:0006104"}


id: PBO:0016533
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by canine rab5","termid":"PBO:0016533"}


id: MONDO:0045020
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease that has its basis in the disruption of glycine metabolic process.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid metabolism disease","termid":"MONDO:0037871"},{"relation_name":"is_a","term_name":"disorder of organic acid metabolism","termid":"MONDO:0045022"}],"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":"glycine metabolism disease","secondary_identifiers":["SCTID:83076007","UMLS:C0268558","MEDGEN:541361"],"synonyms":[{"name":"disorder of glycine metabolic process","type":"exact"},{"name":"disorder of glycine metabolism","type":"exact"},{"name":"glycine metabolic process disease","type":"exact"},{"name":"glycine metabolism disease","type":"exact"}],"termid":"MONDO:0045020","xrefs":{"Monarch":{"xref_id":"0045020"}}}


id: PBO:0070577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 43","termid":"PBO:0070577"}


id: PBO:0060354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin XIX","termid":"PBO:0060354"}


id: GO:0002376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the development or functioning of the immune system, an organismal system for calibrated responses to potential internal or invasive threats.","definition_xrefs":["GOC:add","GO_REF:0000022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_process","termid":"GO:0008150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"immune system process","secondary_identifiers":["Wikipedia:Immune_system"],"termid":"GO:0002376"}


id: PBO:0084002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycerol kinase; converts glycerol to glycerol-3-phosphate; glucose repression of expression is mediated by Adr1p and Ino2p-Ino4p; derepression of expression on non-fermentable carbon sources is mediated by Opi1p and Rsf1p","termid":"PBO:0084002"}


id: MONDO:1011183
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any vitamin D dependent rickets that occurs in dogs due to a mutation in the CYP27B1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"rickets, non-human animal","termid":"MONDO:1011456"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vitamin D dependent rickets, CYP27B1-related, dog","secondary_identifiers":["OMIA:000837-9615"],"synonyms":[{"name":"vitamin D-deficiency rickets type IA, dog","type":"related"}],"termid":"MONDO:1011183","xrefs":{"Monarch":{"xref_id":"1011183"}}}


id: MONDO:0004334
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low or intermediate grade well differentiated tumor with neuroendocrine differentiation that arises from the pancreas. It is characterized by the absence of a hormone-related clinical syndrome.","definition_xrefs":["NCIT:C45837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic neuroendocrine tumor","termid":"MONDO:0019954"},{"relation_name":"is_a","term_name":"non-functioning endocrine neoplasm","termid":"MONDO:0021119"}],"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":"non-functional pancreatic neuroendocrine tumor","secondary_identifiers":["MESH:C536126","MEDGEN:277416","Orphanet:506075","UMLS:C1334977","GARD:22054","DOID:7698","ICDO:8150/3"],"synonyms":[{"name":"inactive pancreatic endocrine tumor","type":"exact"},{"name":"inactive pancreatic endocrine tumour","type":"exact"},{"name":"non functioning pancreatic endocrine tumor","type":"related"},{"name":"non functioning pancreatic endocrine tumour","type":"related"},{"name":"non-functional pancreatic neuroendocrine tumor","type":"exact"},{"name":"non-functioning EPTs","type":"related"},{"name":"non-functioning PNET","type":"exact"},{"name":"non-functioning endocrine pancreatic tumors","type":"related"},{"name":"non-functioning endocrine pancreatic tumours","type":"related"},{"name":"non-functioning neuroendocrine tumor of pancreas","type":"related"},{"name":"non-functioning neuroendocrine tumour of pancreas","type":"related"},{"name":"non-functioning pancreatic NET","type":"exact"},{"name":"non-functioning pancreatic endocrine tumor","type":"exact"},{"name":"non-functioning pancreatic endocrine tumour","type":"exact"},{"name":"non-functioning pancreatic neuroendocrine tumor","type":"exact"},{"name":"non-functioning pancreatic neuroendocrine tumour","type":"exact"},{"name":"non-functioning well differentiated pancreatic endocrine tumor","type":"exact"},{"name":"non-functioning well differentiated pancreatic endocrine tumour","type":"exact"},{"name":"non-functioning well-differentiated NEN of pancreas","type":"exact"},{"name":"non-functioning well-differentiated neuroendocrine neoplasm of pancreas","type":"exact"},{"name":"non-functioning well-differentiated pancreatic NEN","type":"exact"},{"name":"non-functioning well-differentiated pancreatic neuroendocrine neoplasm","type":"exact"},{"name":"non-syndromic pancreatic NET","type":"exact"},{"name":"non-syndromic pancreatic neuroendocrine tumor","type":"exact"},{"name":"non-syndromic pancreatic neuroendocrine tumour","type":"exact"},{"name":"nonfunctional pancreatic NET","type":"exact"},{"name":"nonfunctional pancreatic neuroendocrine tumor","type":"exact"},{"name":"nonfunctional pancreatic neuroendocrine tumour","type":"exact"},{"name":"nonsyndromic pancreatic endocrine tumor","type":"exact"},{"name":"nonsyndromic pancreatic endocrine tumour","type":"exact"},{"name":"nonsyndromic pancreatic neuroendocrine tumor","type":"exact"},{"name":"nonsyndromic pancreatic neuroendocrine tumour","type":"exact"}],"termid":"MONDO:0004334","xrefs":{"Monarch":{"xref_id":"0004334"}}}


id: MONDO:0020155
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete eyelid border anomaly (obsolete MONDO:0020155)","secondary_identifiers":["Orphanet:98564"],"termid":"MONDO:0020155","xrefs":{"Monarch":{"xref_id":"0020155"}}}


id: PBO:0000344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE Sft1 (predicted)","termid":"PBO:0000344"}


id: GO:0031378
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A fatty acid synthase complex in which each polypeptide chain catalyzes a single activity, located in a plastid.","definition_xrefs":["ISBN:0716720094","ISBN:0471331309","GOC:mah","PMID:12957385"],"gene_count":0,"genotype_count":0,"name":"obsolete plastid type II fatty acid synthase complex (obsolete GO:0031378)","synonyms":[{"name":"plastid type II FAS complex","type":"exact"},{"name":"plastid type II fatty acid synthase complex","type":"exact"}],"termid":"GO:0031378"}


id: MONDO:0022612
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Brunsting-Perry syndrome","secondary_identifiers":["MEDGEN:725587","UMLS:C1304226"],"synonyms":[{"name":"Brunsting Perry syndrome","type":"related"},{"name":"cicatricial pemphigoid of the Brunsting-Perry type","type":"related"},{"name":"localised cicatricial pemphigoid","type":"related"},{"name":"localized cicatricial pemphigoid","type":"related"}],"termid":"MONDO:0022612","xrefs":{"Monarch":{"xref_id":"0022612"}}}


id: MONDO:0019025
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A localized tumor consisting of mature mast cells. (WHO, 2001) -- 2003","definition_xrefs":["NCIT:C7136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mastocytoma","termid":"MONDO:0003079"},{"relation_name":"is_a","term_name":"systemic mastocytosis","termid":"MONDO:0016586"}],"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":"extracutaneous mastocytoma","secondary_identifiers":["icd11.foundation:29932455","GARD:18871","MEDGEN:75774","UMLS:C0272202","DOID:4659","SCTID:63175003","ICDO:9740/1","Orphanet:66662"],"synonyms":[{"name":"extracutaneous mastocytoma","type":"exact"}],"termid":"MONDO:0019025","xrefs":{"Monarch":{"xref_id":"0019025"}}}


id: PBO:0071448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 54","termid":"PBO:0071448"}


id: GO:0071971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form an extracellular vesicular exosome, a membrane-bounded vesicle that is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane. Exosomes are defined by their size, which generally ranges from 30 nm to 100 nm.","definition_xrefs":["GOC:tfm","PMID:27462458","GOC:mah","PMID:19442504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle organization","termid":"GO:0016050"},{"relation_name":"is_a","term_name":"organelle assembly","termid":"GO:0070925"},{"relation_name":"part_of","term_name":"extracellular exosome biogenesis","termid":"GO:0097734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"extracellular exosome assembly","synonyms":[{"name":"extracellular vesicular exosome assembly","type":"exact"}],"termid":"GO:0071971"}


id: PBO:0055323
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 2751","termid":"PBO:0055323"}


id: GO:1905397
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process in an activated CD8-positive, alpha-beta T cell.","definition_xrefs":["GO_REF:0000085","GOC:TermGenie","PMID:24187568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell apoptotic process","termid":"GO:0070231"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"activated CD8-positive, alpha-beta T cell apoptotic process","synonyms":[{"name":"activated CD8-positive, alpha-beta T cell apoptosis","type":"narrow"},{"name":"activated CD8-positive, alpha-beta T lymphocyte apoptosis","type":"narrow"},{"name":"activated CD8-positive, alpha-beta T lymphocyte apoptotic process","type":"exact"},{"name":"activated CD8-positive, alpha-beta T-cell apoptosis","type":"narrow"},{"name":"activated CD8-positive, alpha-beta T-cell apoptotic process","type":"exact"},{"name":"activated CD8-positive, alpha-beta T-lymphocyte apoptosis","type":"narrow"},{"name":"activated CD8-positive, alpha-beta T-lymphocyte apoptotic process","type":"exact"}],"termid":"GO:1905397"}


id: MONDO:0025293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute, transmissible, infectious disease associated with high mortality and morbidity in young turkeys (poults). It is characterized by diarrhea; anorexia; growth depression, and immune dysfunction. The cause is unknown but astroviruses (avastrovirus) and coronaviruses (coronavirus, turkey) have been isolated from diseased poults and are thought to cause the enteritis and increased susceptibility to bacterial infections.","definition_xrefs":["MESH:D031261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poultry disease","termid":"MONDO:0025113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poult enteritis mortality syndrome","synonyms":[{"name":"mortality syndrome, spiking","type":"related"},{"name":"spiking mortality syndrome","type":"related"}],"termid":"MONDO:0025293","xrefs":{"Monarch":{"xref_id":"0025293"}}}


id: PBO:0057261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 487a","termid":"PBO:0057261"}


id: SO:0000587
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Group I catalytic introns are large self-splicing ribozymes. They catalyze their own excision from mRNA, tRNA and rRNA precursors in a wide range of organisms. The core secondary structure consists of 9 paired regions (P1-P9). These fold to essentially two domains, the P4-P6 domain (formed from the stacking of P5, P4, P6 and P6a helices) and the P3-P9 domain (formed from the P8, P3, P7 and P9 helices). Group I catalytic introns often have long ORFs inserted in loop regions.","direct_ancestors":[{"relation_name":"is_a","term_name":"autocatalytically_spliced_intron","termid":"SO:0000588"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"group_I_intron","secondary_identifiers":["http://en.wikipedia.org/wiki/Group_I_intron"],"synonyms":[{"name":"group I intron","type":"exact"}],"termid":"SO:0000587"}


id: PBO:0066899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 199","termid":"PBO:0066899"}


id: PATO:0000854
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000854 contact righting reflex value (obsolete PATO:0000854)","termid":"PATO:0000854"}


id: GO:1900498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of butyryl-CoA catabolic process to butanol.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of amide metabolic process","termid":"GO:0034249"},{"relation_name":"is_a","term_name":"negative regulation of fatty acid metabolic process","termid":"GO:0045922"},{"relation_name":"is_a","term_name":"negative regulation of nucleobase-containing compound metabolic process","termid":"GO:0045934"},{"relation_name":"is_a","term_name":"negative regulation of phosphate metabolic process","termid":"GO:0045936"},{"relation_name":"is_a","term_name":"negative regulation of lipid catabolic process","termid":"GO:0050995"},{"relation_name":"is_a","term_name":"negative regulation of lipid biosynthetic process","termid":"GO:0051055"},{"relation_name":"is_a","term_name":"negative regulation of sulfur metabolic process","termid":"GO:0051175"},{"relation_name":"is_a","term_name":"regulation of butyryl-CoA catabolic process to butanol","termid":"GO:1900497"},{"relation_name":"is_a","term_name":"negative regulation of alcohol biosynthetic process","termid":"GO:1902931"},{"relation_name":"negatively_regulates","term_name":"butyryl-CoA catabolic process to butanol","termid":"GO:0044582"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044248"},{"rel_name":"negatively_regulates","termid":"GO:0055086"},{"rel_name":"negatively_regulates","termid":"GO:0006790"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044248"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044248","GO:0006629","GO:0008150","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"negative regulation of butyryl-CoA catabolic process to butanol","synonyms":[{"name":"down regulation of butyryl-CoA catabolic process to butanol","type":"exact"},{"name":"down regulation of butyryl-CoA catabolism to butanol","type":"exact"},{"name":"down-regulation of butyryl-CoA catabolic process to butanol","type":"exact"},{"name":"down-regulation of butyryl-CoA catabolism to butanol","type":"exact"},{"name":"downregulation of butyryl-CoA catabolic process to butanol","type":"exact"},{"name":"downregulation of butyryl-CoA catabolism to butanol","type":"exact"},{"name":"inhibition of butyryl-CoA catabolic process to butanol","type":"narrow"},{"name":"inhibition of butyryl-CoA catabolism to butanol","type":"exact"},{"name":"negative regulation of butyryl-CoA catabolism to butanol","type":"exact"}],"termid":"GO:1900498"}


id: GO:0098626
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADPH + H+ + CH3SeO2H => NADP+ + CH3SeOH + H2O.","definition_xrefs":["PMID:11782468"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H","termid":"GO:0016651"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"methylseleninic acid reductase activity","secondary_identifiers":["Reactome:R-HSA-5263616"],"termid":"GO:0098626"}


id: PBO:0081162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger RNA binding protein pseudogene 1","termid":"PBO:0081162"}


id: MONDO:0009879
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Short stature due to growth hormone qualitative anomaly is characterized by growth retardation and short stature (despite the presence of normal or slightly elevated levels of immunoreactive growth hormone, GH), low concentrations of insulin-like growth factor-I (IGF-I) and a significant increase in growth rate following recombinant GH therapy. Prevalence is unknown but only a few cases have been reported in the literature. The syndrome is caused by various mutations in the GH1 gene (17q22-q24) that result in structural GH anomalies and a biologically inactive molecule. Transmission is autosomal recessive.","definition_xrefs":["Orphanet:629"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated congenital growth hormone deficiency","termid":"MONDO:0000050"}],"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":"short stature due to growth hormone qualitative anomaly","secondary_identifiers":["MEDGEN:340412","OMIM:262650","MESH:C537505","GARD:408","icd11.foundation:1665498704","UMLS:C1849779"],"synonyms":[{"name":"Biodefective Growth hormone","type":"related"},{"name":"KOWARSKI syndrome","type":"related"},{"name":"Kowarski syndrome","type":"exact"},{"name":"pituitary dwarfism with normal immunoreactive Growth hormone and Low Somatomedin","type":"related"}],"termid":"MONDO:0009879","xrefs":{"Monarch":{"xref_id":"0009879"}}}


id: GO:0043190
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex for the transport of metabolites into and out of the cell, typically comprised of four domains; two membrane-associated domains and two ATP-binding domains at the intracellular face of the membrane, that form a central pore through the plasma membrane. Each of the four core domains may be encoded as a separate polypeptide or the domains can be fused in any one of a number of ways into multidomain polypeptides. In Bacteria and Archaebacteria, ABC transporters also include substrate binding proteins to bind substrate external to the cytoplasm and deliver it to the transporter.","definition_xrefs":["PMID:11421269","PMID:15111107","GOC:mtg_sensu","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase dependent transmembrane transport complex","termid":"GO:0098533"},{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"ATP-binding cassette (ABC) transporter complex","secondary_identifiers":["GO:0043192","GO:0043191"],"synonyms":[{"name":"ABC-type efflux permease complex","type":"narrow"},{"name":"ABC-type efflux porter complex","type":"narrow"},{"name":"ABC-type uptake permease complex","type":"narrow"},{"name":"mating pheromone exporter","type":"narrow"}],"termid":"GO:0043190"}


id: PBO:0079039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon CAC) 1-1","termid":"PBO:0079039"}


id: PBO:0011972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA recombination protein Rad22 (previously Rad52)","termid":"PBO:0011972"}


id: PBO:0036195
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_chromatin_during_mitotic_G1_phase","termid":"PBO:0036195"}


id: GO:0102393
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: FAD + H+ + a decanoyl-HmqF protein = FADH2(2-) + a 2,3-dehydro-decanoyl-HmqF.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete decanoyl-[acp] 2-dehydrogenase activity (obsolete GO:0102393)","termid":"GO:0102393"}


id: PBO:0073576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shisa family member 7","termid":"PBO:0073576"}


id: GO:1904192
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cholangiocyte apoptotic process.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:24498161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell apoptotic process","termid":"GO:1904035"},{"relation_name":"regulates","term_name":"cholangiocyte apoptotic process","termid":"GO:1902488"}],"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 cholangiocyte apoptotic process","synonyms":[{"name":"regulation of cholangiocyte apoptosis","type":"narrow"},{"name":"regulation of epithelial cell of bile duct apoptosis","type":"narrow"},{"name":"regulation of epithelial cell of bile duct apoptotic process","type":"exact"}],"termid":"GO:1904192"}


id: PBO:0029261
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_transmembrane_transport_gene_mRNA_during_vegetative_growth","termid":"PBO:0029261"}


id: MONDO:1012137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital joint laxity and dwarfism, non-human animal","termid":"MONDO:1011946"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital joint laxity and dwarfism, cattle","secondary_identifiers":["OMIA:000570-9913"],"termid":"MONDO:1012137","xrefs":{"Monarch":{"xref_id":"1012137"}}}


id: MONDO:0009139
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"}],"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":"dyssegmental dysplasia, Rolland-Desbuquois type","secondary_identifiers":["ICD9:756.59","Orphanet:156731","OMIM:224400","SCTID:95243004","MESH:C537999","GARD:9810","UMLS:C0432209","icd11.foundation:1291444727","MEDGEN:98145"],"synonyms":[{"name":"Anisospondylic Camptomicromelic dwarfism, Rolland-Desbuquois type","type":"related"},{"name":"Anisospondylic camptomicromelic dwarfism Rolland-Desbuquois type","type":"related"},{"name":"Ddrd","type":"related"},{"name":"dyssegmental dwarfism Rolland-Desbuquois type","type":"related"},{"name":"dyssegmental dwarfism, Rolland-Desbuquois type","type":"related"},{"name":"dyssegmental dysplasia Rolland-Desbuquois type","type":"related"},{"name":"dyssegmental dysplasia, Rolland-Desbuquois type","type":"exact"}],"termid":"MONDO:0009139","xrefs":{"Monarch":{"xref_id":"0009139"}}}


id: PBO:0028939
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cell_growth","termid":"PBO:0028939"}


id: GO:1900603
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving tensidol A.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"tensidol A metabolic process","synonyms":[{"name":"tensidol A metabolism","type":"exact"}],"termid":"GO:1900603"}


id: PBO:0072419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 24","termid":"PBO:0072419"}


id: PBO:0113116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endosomal protein involved in endocytosis and autophagy; homologous to Chediak-Higashi syndrome and Beige proteins, both of which are implicated in disease syndromes in human and mouse, respectively, due to defective lysosomal trafficking; mutant phenotype and genetic interactions suggest a role in protein sorting","termid":"PBO:0113116"}


id: MONDO:0957408
data:
  {"annotated_genes":["SJAG_00400","SJAG_04541","SJAG_03805","SJAG_05239","SJAG_03151","SJAG_01884","SJAG_04380","SJAG_04569","SJAG_04290","SJAG_04118","SJAG_02039","SJAG_04969"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012429"},{"annotations":[84948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012471"},{"annotations":[84951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012472"},{"annotations":[85037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014007"},{"annotations":[87045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014629"},{"annotations":[86517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054698"},{"annotations":[86328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054700"},{"annotations":[85201,85200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054699"},{"annotations":[86202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024541"},{"annotations":[86053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013818"},{"annotations":[85419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010523"}]},"cv_name":"mondo","definition":"A type 1 interferonopathy that occurs during childhood.","definition_xrefs":["MONDO:patterns/childhood"],"direct_ancestors":[{"relation_name":"is_a","term_name":"type 1 interferonopathy","termid":"MONDO:0700264"},{"relation_name":"is_a","term_name":"autoinflammatory syndrome of childhood","termid":"MONDO:0957018"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00400":null,"SJAG_01884":null,"SJAG_02039":null,"SJAG_03151":null,"SJAG_03805":null,"SJAG_04118":null,"SJAG_04290":null,"SJAG_04380":null,"SJAG_04541":null,"SJAG_04569":null,"SJAG_04969":null,"SJAG_05239":null},"genotype_count":0,"is_obsolete":false,"name":"type 1 interferonopathy of childhood","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5681250","GARD:21986","MEDGEN:1843010","Orphanet:481671"],"termid":"MONDO:0957408","terms_by_termid":{"MONDO:0010523":null,"MONDO:0012429":null,"MONDO:0012471":null,"MONDO:0012472":null,"MONDO:0013818":null,"MONDO:0014007":null,"MONDO:0014629":null,"MONDO:0024541":null,"MONDO:0054698":null,"MONDO:0054699":null,"MONDO:0054700":null},"xrefs":{"Monarch":{"xref_id":"0957408"}}}


id: PBO:0040776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bestrophin 2","termid":"PBO:0040776"}


id: PR:O42972
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC20F10.02c gene.","definition_xrefs":["UniProtKB:O42972","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":"UPF0588 membrane protein C20F10.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC20F10.02c","synonyms":[{"name":"Spom972h-SPBC20F10.02c","type":"exact"}],"termid":"PR:O42972"}


id: MONDO:1012818
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital hypotrichosis that occurs in cats due to a mutation in the HR gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypotrichosis, non-human animal","termid":"MONDO:1012977"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis, HR-related, domestic cat","secondary_identifiers":["OMIA:002229-9685"],"termid":"MONDO:1012818","xrefs":{"Monarch":{"xref_id":"1012818"}}}


id: PBO:0050362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 65","termid":"PBO:0050362"}


id: PR:O94355
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rxt2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94355"],"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 regulatory protein rxt2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC428.06c","synonyms":[{"name":"Spom972h-rxt2","type":"exact"}],"termid":"PR:O94355"}


id: PBO:0049108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 165, pseudogene","termid":"PBO:0049108"}


id: PBO:0057112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 200a","termid":"PBO:0057112"}


id: GO:0019209
data:
  {"annotated_genes":["SJAG_02785","SJAG_04614","SJAG_00296","SJAG_03936","SJAG_00457","SJAG_02332","SJAG_01411","SJAG_00439","SJAG_00424","SJAG_03340","SJAG_02026","SJAG_03371","SJAG_04020","SJAG_04509","SJAG_01401","SJAG_02605","SJAG_04666","SJAG_03699","SJAG_03695","SJAG_05017","SJAG_03090","SJAG_01000","SJAG_00333","SJAG_01605","SJAG_01213","SJAG_00318","SJAG_04502","SJAG_02232","SJAG_04200","SJAG_00142","SJAG_00236","SJAG_02057","SJAG_03618","SJAG_04140","SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098744"},{"annotations":[91905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019912"},{"annotations":[112713,73785,70086,65923,110954,116816,101379,79545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061575"},{"annotations":[72721,106900,116063,69971,88979,98955,78209,70224,71963,111185,91073,112229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030295"},{"annotations":[90953,104887,109024,110296,90622,75318,88994,75312,118111,87669,92195,89202,68691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043539"}]},"cv_name":"molecular_function","definition":"Binds to and increases the activity of a kinase, an enzyme which catalyzes of the transfer of a phosphate group, usually from ATP, to a substrate molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme activator activity","termid":"GO:0008047"},{"relation_name":"is_a","term_name":"kinase regulator activity","termid":"GO:0019207"}],"gene_count":35,"genes_by_uniquename":{"SJAG_00142":null,"SJAG_00236":null,"SJAG_00296":null,"SJAG_00318":null,"SJAG_00333":null,"SJAG_00424":null,"SJAG_00439":null,"SJAG_00457":null,"SJAG_01000":null,"SJAG_01213":null,"SJAG_01401":null,"SJAG_01411":null,"SJAG_01605":null,"SJAG_02026":null,"SJAG_02057":null,"SJAG_02232":null,"SJAG_02332":null,"SJAG_02605":null,"SJAG_02785":null,"SJAG_03090":null,"SJAG_03340":null,"SJAG_03371":null,"SJAG_03453":null,"SJAG_03618":null,"SJAG_03695":null,"SJAG_03699":null,"SJAG_03936":null,"SJAG_04020":null,"SJAG_04140":null,"SJAG_04200":null,"SJAG_04502":null,"SJAG_04509":null,"SJAG_04614":null,"SJAG_04666":null,"SJAG_05017":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140677"}],"interesting_parent_ids":["GO:0003674","GO:0030234","GO:0140677","GO:0098772"],"is_obsolete":false,"name":"kinase activator activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0019209","terms_by_termid":{"GO:0019912":null,"GO:0030295":null,"GO:0043539":null,"GO:0061575":null,"GO:0098744":null}}


id: PBO:0029163
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_phosphorylation","termid":"PBO:0029163"}


id: FYPO:0001249
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which the probability that a DNA replication will initiate at a particular replication origin is higher than in wild type. In cells with increased origin firing efficiency, genomic DNA replication initiates from more origins than wild type, and is completed in more, smaller segments, than wild type.","definition_xrefs":["PMID:18799612","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of mitotic DNA replication initiation","termid":"FYPO:0001248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased origin firing efficiency","synonyms":[{"name":"increased origin firing efficiency during mitotic cell cycle","type":"related"},{"name":"increased origin firing efficiency during vegetative growth","type":"exact"}],"termid":"FYPO:0001249"}


id: GO:0044646
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant modulation of complement activation in the bitten/stung organism.","definition_xrefs":["PMID:20837040","GOC:jl","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete envenomation resulting in modulation of complement activation in another organism (obsolete GO:0044646)","synonyms":[{"name":"envenomation resulting in modulation of complement activation in other organism","type":"exact"},{"name":"envenomation resulting in regulation of complement activation in other organism","type":"exact"}],"termid":"GO:0044646"}


id: PBO:0039126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apoptosis inducing factor mitochondria associated 3","termid":"PBO:0039126"}


id: PBO:0030684
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-tapered_vegetative_cell","termid":"PBO:0030684"}


id: PBO:0086215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that binds to Fpr1p; confers rapamycin resistance by competing with rapamycin for Fpr1p binding; accumulates in the nucleus upon treatment of cells with rapamycin; has similarity to D. melanogaster shuttle craft and human NFX1","termid":"PBO:0086215"}


id: PBO:0031553
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_peptidase_activity","termid":"PBO:0031553"}


id: GO:0031053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process involved in the conversion of a primary microRNA transcript into a pre-microRNA molecule.","definition_xrefs":["GOC:sl","PMID:25799998","PMID:15211354"],"direct_ancestors":[{"relation_name":"is_a","term_name":"miRNA processing","termid":"GO:0035196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"primary miRNA processing","secondary_identifiers":["GO:1990729","GO:1990744"],"synonyms":[{"name":"pri-miRNA processing","type":"exact"},{"name":"primary miRNA methylation","type":"narrow"},{"name":"primary miRNA modification","type":"exact"},{"name":"primary microRNA processing","type":"exact"}],"termid":"GO:0031053"}


id: MONDO:0015735
data:
  {"annotated_genes":["SJAG_03379","SJAG_03145"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85061],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008070"},{"annotations":[86494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009725"}]},"cv_name":"mondo","definition":"Severe congenital nemaline myopathy is a severe form of nemaline myopathy (NM) characterized by severe hypotonia with little spontaneous movement in neonates.","definition_xrefs":["Orphanet:171430"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of alpha-actin","termid":"MONDO:0016193"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of nebulin","termid":"MONDO:0016194"},{"relation_name":"is_a","term_name":"nemaline myopathy","termid":"MONDO:0018958"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03145":null,"SJAG_03379":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"severe congenital nemaline myopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:12821","icd11.foundation:1025202057","MEDGEN:1805110","UMLS:C5680451"],"synonyms":[{"name":"severe congenital (neonatal) NM","type":"related"}],"termid":"MONDO:0015735","terms_by_termid":{"MONDO:0008070":null,"MONDO:0009725":null},"xrefs":{"Monarch":{"xref_id":"0015735"}}}


id: PR:Q9P7X3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- frg1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7X3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein frg1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP23A10.12","synonyms":[{"name":"Spom972h-frg1","type":"exact"}],"termid":"PR:Q9P7X3"}


id: PBO:0026988
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_nigericin","termid":"PBO:0026988"}


id: GO:0090121
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disassembly into constituent parts of the low-density lipoprotein particle in the lysosome that contributes to cholesterol transport.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"low-density lipoprotein particle disassembly","termid":"GO:0090495"},{"relation_name":"part_of","term_name":"cholesterol transport","termid":"GO:0030301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"low-density lipoprotein particle disassembly involved in cholesterol transport","termid":"GO:0090121"}


id: GO:0061119
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of directed movement of a motile cell or organism up a concentration gradient of 3',5'-cAMP by the action of a chlorinated alkylphenone. An alkylphenone is an aromatic polyketide with methyl and chlorine substitutions.","definition_xrefs":["GOC:dph","PMID:19684855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of positive chemotaxis to cAMP","termid":"GO:0061118"}],"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 positive chemotaxis to cAMP by chlorinated alkylphenone","termid":"GO:0061119"}


id: PBO:0050283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histocompatibility minor serpin domain containing","termid":"PBO:0050283"}


id: PBO:0082995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic leucyl tRNA synthetase; ligates leucine to the appropriate tRNA; human homolog LARS can complement yeast temperature-sensitive mutant at restrictive temperature","termid":"PBO:0082995"}


id: GO:0021950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation and reception of signals that repel a precerebellar neuron as a component of the process of tangential migration.","definition_xrefs":["GOC:cls","GO_REF:0000021","GOC:dph","GOC:jid","PMID:15157725","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative chemotaxis","termid":"GO:0050919"},{"relation_name":"part_of","term_name":"brainstem precerebellar neuron precursor migration","termid":"GO:0021949"}],"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":"chemorepulsion involved in precerebellar neuron migration","synonyms":[{"name":"negative chemotaxis involved in precerebellar neuron migration","type":"exact"}],"termid":"GO:0021950"}


id: PBO:0084761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial methionyl-tRNA synthetase (MetRS); functions as a monomer in mitochondrial protein synthesis; functions similarly to cytoplasmic MetRS although the cytoplasmic form contains a zinc-binding domain not found in Msm1p","termid":"PBO:0084761"}


id: PBO:0075947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stromal antigen 3-like 2 (pseudogene)","termid":"PBO:0075947"}


id: PBO:0049118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 183","termid":"PBO:0049118"}


id: PBO:0063730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatase and actin regulator 3","termid":"PBO:0063730"}


id: MONDO:0019973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent placoid maculopathy is characterized by white plaque-like lesions involving the macula but sparing the peripapillary areas of both eyes. It has been described in five patients. In contrast to patients with macular serpiginous choroiditis presenting with similar lesions, the five patients reported so far with persistent placoid maculopathy had good visual acuity until the onset of choroidal neovascularization (CNV) or pigmentary mottling. The macular lesions fade after several months or years, but the vascular anomalies persist leading to a loss of central vision.","definition_xrefs":["Orphanet:97341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"}],"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":"persistent placoid maculopathy","secondary_identifiers":["GARD:19369","SCTID:719297006","MEDGEN:930492","UMLS:C4304823","icd11.foundation:1143591468"],"termid":"MONDO:0019973","xrefs":{"Monarch":{"xref_id":"0019973"}}}


id: GO:0060867
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled shedding of a fruit.","definition_xrefs":["GOC:dph","GOC:sdb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abscission","termid":"GO:0009838"}],"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":"fruit abscission","termid":"GO:0060867"}


id: MONDO:0014077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cobblestone lissencephaly without muscular or ocular involvement is a form of cobblestone lissencephaly characterized by a constellation of brain malformations which can either exist alone or in conjunction with minimal muscular and ocular abnormalities. The clinical features of the disease include severe developmental delay, increased head circumference, hydrocephalus and seizures.","definition_xrefs":["Orphanet:352682"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cobblestone lissencephaly","termid":"MONDO:0018869"}],"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":"cobblestone lissencephaly without muscular or ocular involvement","secondary_identifiers":["DOID:0112230","UMLS:C3554657","GARD:17526","MEDGEN:767571","OMIM:615191"],"synonyms":[{"name":"LIS5","type":"related"},{"name":"cobblestone lissencephaly without muscular or eye involvement","type":"exact"},{"name":"cobblestone lissencephaly without muscular or ocular involvement","type":"exact"},{"name":"lissencephaly 5","type":"related"},{"name":"lissencephaly type 2 without muscular or eye involvement","type":"exact"},{"name":"lissencephaly type 2 without muscular or ocular involvement","type":"exact"},{"name":"lissencephaly type 5","type":"exact"}],"termid":"MONDO:0014077","xrefs":{"Monarch":{"xref_id":"0014077"}}}


id: GO:0017020
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and modulates of the activity of myosin phosphatase.","definition_xrefs":["GOC:ai","PMID:10491107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein phosphatase regulator activity","termid":"GO:0019888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0030234","GO:0098772","GO:0003674"],"is_obsolete":false,"name":"myosin phosphatase regulator activity","synonyms":[{"name":"myosin phosphatase, intrinsic regulator activity","type":"narrow"}],"termid":"GO:0017020"}


id: MONDO:0013764
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the TMEM138 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome with oculorenal defect","termid":"MONDO:0009480"},{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559","MONDO:0020022"],"is_obsolete":false,"name":"Joubert syndrome 16","secondary_identifiers":["OMIM:614465","DOID:0110985","UMLS:C3280906","GARD:15807","MEDGEN:482536"],"synonyms":[{"name":"JBTS16","type":"exact"},{"name":"Joubert syndrome 16","type":"exact"},{"name":"Joubert syndrome caused by mutation in TMEM138","type":"exact"},{"name":"Joubert syndrome type 16","type":"exact"},{"name":"TMEM138 Joubert syndrome","type":"exact"}],"termid":"MONDO:0013764","xrefs":{"Monarch":{"xref_id":"0013764"}}}


id: GO:0034467
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of an esterosome.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle lumen","termid":"GO:0060205"},{"relation_name":"part_of","term_name":"esterosome","termid":"GO:0033117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"esterosome lumen","termid":"GO:0034467"}


id: FYPO:0003086
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of chromatin binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein complex binding","termid":"FYPO:0005232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000702","FYPO:0000257"],"is_obsolete":false,"name":"normal chromatin binding","termid":"FYPO:0003086"}


id: SO:0001386
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A post translationally modified glycine amino acid feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_amino_acid_feature","termid":"SO:0001385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_glycine","secondary_identifiers":["MOD:00908"],"synonyms":[{"name":"ModGly","type":"exact"},{"name":"modified glycine","type":"exact"}],"termid":"SO:0001386"}


id: GO:0016298
data:
  {"annotated_genes":["SJAG_04292","SJAG_00321","SJAG_04323","SJAG_02907","SJAG_02100","SJAG_04105","SJAG_02068","SJAG_00199","SJAG_01519","SJAG_03604","SJAG_02091","SJAG_01219","SJAG_02487","SJAG_01036","SJAG_01198","SJAG_02093","SJAG_04790","SJAG_04973","SJAG_04110","SJAG_02161","SJAG_02543","SJAG_00158","SJAG_02715","SJAG_02089","SJAG_03204"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98575],"is_not":false,"summary":null,"term":"GO:0016298"},{"annotations":[64803,113804,65776,67337,70423,93685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004622"},{"annotations":[108576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052714"},{"annotations":[77055,78155,70743,78604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047372"},{"annotations":[97525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034479"},{"annotations":[72428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004435"},{"annotations":[70784,77077,78327,76288],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004623"},{"annotations":[77761,75604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004620"},{"annotations":[74114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004630"},{"annotations":[63060],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004767"},{"annotations":[74720,77085,74662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004771"},{"annotations":[98225,58247,69439,59743,93686,71169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004806"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a lipid.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on ester bonds","termid":"GO:0016788"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00158":null,"SJAG_00199":null,"SJAG_00321":null,"SJAG_01036":null,"SJAG_01198":null,"SJAG_01219":null,"SJAG_01519":null,"SJAG_02068":null,"SJAG_02089":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02100":null,"SJAG_02161":null,"SJAG_02487":null,"SJAG_02543":null,"SJAG_02715":null,"SJAG_02907":null,"SJAG_03204":null,"SJAG_03604":null,"SJAG_04105":null,"SJAG_04110":null,"SJAG_04292":null,"SJAG_04323":null,"SJAG_04790":null,"SJAG_04973":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"lipase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-163432","Reactome:R-HSA-163402"],"termid":"GO:0016298","terms_by_termid":{"GO:0004435":null,"GO:0004620":null,"GO:0004622":null,"GO:0004623":null,"GO:0004630":null,"GO:0004767":null,"GO:0004771":null,"GO:0004806":null,"GO:0016298":null,"GO:0034479":null,"GO:0047372":null,"GO:0052714":null}}


id: GO:0031226
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the plasma membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of plasma membrane (obsolete GO:0031226)","synonyms":[{"name":"intrinsic to plasma membrane","type":"narrow"}],"termid":"GO:0031226"}


id: PBO:0002691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triose phosphate transporter (predicted)","termid":"PBO:0002691"}


id: GO:0009502
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A series of membrane-linked oxidation-reduction reactions in which electrons are transferred from an initial electron donor through a series of intermediates to a final electron acceptor (usually oxygen).","definition_xrefs":["GOC:mtg_electron_transport","ISBN:0140514031"],"gene_count":0,"genotype_count":0,"name":"obsolete photosynthetic electron transport chain (obsolete GO:0009502)","synonyms":[{"name":"photosynthetic electron transport chain","type":"exact"}],"termid":"GO:0009502"}


id: PBO:0050141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 51","termid":"PBO:0050141"}


id: GO:0050216
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD+ + propane-1,2-diol 1-phosphate = H+ + hydroxyacetone phosphate + NADH.","definition_xrefs":["RHEA:21584","EC:1.1.1.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"propanediol-phosphate dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R04236","MetaCyc:PROPANEDIOL-PHOSPHATE-DEHYDROGENASE-RXN"],"termid":"GO:0050216"}


id: PBO:0045847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 37","termid":"PBO:0045847"}


id: PBO:0053157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"low density lipoprotein receptor","termid":"PBO:0053157"}


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


id: GO:0160201
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bounded organelle found in a microsporidian spore,  that swells with water, and exerts pressure to rupture the polar cap and evert the polar tube through which the sporoplasm escapes to infect the host.","definition_xrefs":["PMID:16005007","Wikipedia:polaroplast","PMID:19673893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membrane-bounded organelle","termid":"GO:0043231"}],"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":"polaroplast","termid":"GO:0160201"}


id: PBO:0042522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 2 associated protein 2","termid":"PBO:0042522"}


id: PBO:0064608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POU class 4 homeobox 2","termid":"PBO:0064608"}


id: PBO:0039211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldo-keto reductase family 1 member C2","termid":"PBO:0039211"}


id: GO:1900152
data:
  {"annotated_genes":["SJAG_02370"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91433],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060212"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay.","definition_xrefs":["GOC:TermGenie","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","termid":"GO:1900151"},{"relation_name":"is_a","term_name":"negative regulation of mRNA catabolic process","termid":"GO:1902373"},{"relation_name":"negatively_regulates","term_name":"nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","termid":"GO:0000288"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02370":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0016071","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"down regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"down regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"down-regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"down-regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"downregulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"downregulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"inhibition of deadenylation-dependent mRNA decay","type":"narrow"},{"name":"inhibition of mRNA breakdown, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of mRNA catabolic process, deadenylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolic process, deadenylylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolism, deadenylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolism, deadenylylation-dependent","type":"narrow"},{"name":"inhibition of mRNA degradation, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"narrow"},{"name":"negative regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"negative regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"negative regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"negative regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"negative regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"}],"termid":"GO:1900152","terms_by_termid":{"GO:0060212":null}}


