# terms

id: GO:0044685
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: tetrahydromethanopterin + L-serine = 5,10-methylenetetrahydromethanopterin + glycine + H2O.","definition_xrefs":["PMID:12902326","GOC:mengo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete tetrahydromethanopterin-dependent serine hydroxymethyltransferase activity (obsolete GO:0044685)","termid":"GO:0044685"}


id: GO:0102806
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-coumaryl-CoA + cyanin betaine = shisonin + coenzyme A.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4-coumaroyl-CoA:cyanidin-3,5-diglucoside-6''-O-acyltransferase activity (obsolete GO:0102806)","termid":"GO:0102806"}


id: GO:0034209
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of an acetyl group to a sterol molecule. An acetyl group is CH3CO-, derived from acetic [ethanoic] acid.","definition_xrefs":["GOC:rb","PMID:18034159"],"gene_count":0,"genotype_count":0,"name":"obsolete sterol acetylation (obsolete GO:0034209)","termid":"GO:0034209"}


id: PBO:0056532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylcrotonyl-CoA carboxylase subunit 1","termid":"PBO:0056532"}


id: GO:0008840
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pyruvate + L-aspartate-4-semialdehyde = (2S,4S)-4-hydroxy-2,3,4,5-tetrahydrodipicolinate + H2O.","definition_xrefs":["PMID:8993314","RHEA:34171"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"4-hydroxy-tetrahydrodipicolinate synthase activity","secondary_identifiers":["MetaCyc:DIHYDRODIPICSYN-RXN","EC:4.3.3.7","KEGG_REACTION:R02292"],"synonyms":[{"name":"DHDPS activity","type":"related"},{"name":"L-aspartate-4-semialdehyde hydro-lyase (adding pyruvate and cyclizing)","type":"related"},{"name":"L-aspartate-4-semialdehyde hydro-lyase [adding pyruvate and cyclizing; (S)-2,3-dihydropyridine-2,6-dicarboxylate-forming]","type":"related"},{"name":"dihydrodipicolinate synthase activity","type":"exact"},{"name":"dihydrodipicolinate synthetase activity","type":"related"},{"name":"dihydrodipicolinic acid synthase activity","type":"related"}],"termid":"GO:0008840"}


id: PBO:0050905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon induced protein 44","termid":"PBO:0050905"}


id: GO:0065009
data:
  {"annotated_genes":["SJAG_03088","SJAG_04887"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105476,95615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904530"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a molecular function, an elemental biological activity occurring at the molecular level, such as catalysis or binding.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological regulation","termid":"GO:0065007"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03088":null,"SJAG_04887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of molecular function","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of a molecular function","type":"exact"}],"termid":"GO:0065009","terms_by_termid":{"GO:1904530":null}}


id: GO:0051020
data:
  {"annotated_genes":["SJAG_01943","SJAG_03229","SJAG_03693","SJAG_03959","SJAG_03002","SJAG_02012","SJAG_04733","SJAG_00968","SJAG_04400","SJAG_02661","SJAG_04366","SJAG_02974","SJAG_01358","SJAG_03662","SJAG_02833","SJAG_02998","SJAG_00279","SJAG_00864","SJAG_01909","SJAG_01789","SJAG_03085","SJAG_00525","SJAG_03470","SJAG_04703"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74330],"is_not":false,"summary":null,"term":"GO:0051020"},{"annotations":[72201,64781,59119,61098,64029,66776,69067,75313,69140,71605,67768,61730,58816,64956,77964,63216,73810,78521,57286,61624,64953,60453,74283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031267"}]},"cv_name":"molecular_function","definition":"Binding to a GTPase, any enzyme that catalyzes the hydrolysis of GTP.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":24,"genes_by_uniquename":{"SJAG_00279":null,"SJAG_00525":null,"SJAG_00864":null,"SJAG_00968":null,"SJAG_01358":null,"SJAG_01789":null,"SJAG_01909":null,"SJAG_01943":null,"SJAG_02012":null,"SJAG_02661":null,"SJAG_02833":null,"SJAG_02974":null,"SJAG_02998":null,"SJAG_03002":null,"SJAG_03085":null,"SJAG_03229":null,"SJAG_03470":null,"SJAG_03662":null,"SJAG_03693":null,"SJAG_03959":null,"SJAG_04366":null,"SJAG_04400":null,"SJAG_04703":null,"SJAG_04733":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"GTPase binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"termid":"GO:0051020","terms_by_termid":{"GO:0031267":null,"GO:0051020":null}}


id: MONDO:0859575
data:
  {"annotated_genes":["SJAG_00213"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85939],"is_not":false,"summary":null,"term":"MONDO:0859575"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mosaic variegated aneuploidy syndrome","termid":"MONDO:0000141"},{"relation_name":"is_a","term_name":"Atelis syndrome","termid":"MONDO:0859393"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00213":null},"genotype_count":0,"is_obsolete":false,"name":"Atelis syndrome 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1824054","OMIM:620184","UMLS:C5774281"],"termid":"MONDO:0859575","terms_by_termid":{"MONDO:0859575":null},"xrefs":{"Monarch":{"xref_id":"0859575"}}}


id: MONDO:0005201
data:
  {"annotated_genes":["SJAG_02131","SJAG_00930","SJAG_03824"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030330"},{"annotations":[85556,85555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009290"}]},"cv_name":"mondo","definition":"A type of heart disorder referring to the inability of the ventricles to fill with blood because the myocardium (heart muscle) stiffens and looses its flexibility. Causes include replacement of the myocardium with scar tissue, abnormal cellular infiltration of the myocardium, or deposition of a substance (e.g., amyloid) in the myocardium.","definition_xrefs":["NCIT:C62798"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intrinsic cardiomyopathy","termid":"MONDO:0000591"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00930":null,"SJAG_02131":null,"SJAG_03824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"restrictive cardiomyopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:20531","icd11.foundation:316495940","DOID:397","EFO:0002630","NANDO:2200233","UMLS:C0007196","NANDO:1200292","MedDRA:10038748","NANDO:1200293","MEDGEN:40111","Orphanet:217632","ICD9:425.4","NANDO:2100058","SCTID:415295002","MESH:D002313"],"synonyms":[{"name":"cardiomyopathy, constrictive","type":"exact"},{"name":"familial restrictive cardiomyopathy","type":"narrow"},{"name":"primary restrictive cardiomyopathy","type":"exact"},{"name":"restrictive cardiomyopathy","type":"exact"}],"termid":"MONDO:0005201","terms_by_termid":{"MONDO:0009290":null,"MONDO:0030330":null},"xrefs":{"Monarch":{"xref_id":"0005201"}}}


id: GO:0038144
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric complex between the tyrosine kinase receptor ERBB2 and a ligand-activated receptor ERBB4. ERBB2, which does not bind any known ligand, is activated through formation of a heterodimer with another ligand-activated ERBB family member such as ERBB4.","definition_xrefs":["PMID:16978839","PMID:16460914","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane signaling receptor complex","termid":"GO:0098802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"ERBB4:ERBB2 complex","synonyms":[{"name":"ERBB4:ERBB2 heterodimer","type":"narrow"},{"name":"NRGs/EGFLs:ERBB4:ERBB2","type":"narrow"}],"termid":"GO:0038144"}


id: PBO:0041196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BUD13 homolog","termid":"PBO:0041196"}


id: FYPO:0007799
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 a protein that is not normally found at the cell surface is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized protein during vegetative growth","termid":"FYPO:0000782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"protein mislocalized to cell surface during vegetative growth","synonyms":[{"name":"ectopic protein localization to cell surface during vegetative growth","type":"exact"},{"name":"protein mislocalised to cell surface during vegetative growth","type":"exact"},{"name":"protein mislocalized to cell surface during mitotic cell cycle","type":"related"}],"termid":"FYPO:0007799"}


id: PBO:0034255
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-lays_eggs_in","termid":"PBO:0034255"}


id: GO:0009622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete resistance to pathogenic fungi (obsolete GO:0009622)","synonyms":[{"name":"resistance to pathogenic fungi","type":"exact"}],"termid":"GO:0009622"}


id: SO:0000481
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An inverted repeat (SO:0000294) occurring at the termini of a DNA transposon.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inverted_repeat","termid":"SO:0000294"},{"relation_name":"part_of","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"terminal_inverted_repeat","synonyms":[{"name":"TIR","type":"exact"},{"name":"terminal inverted repeat","type":"exact"}],"termid":"SO:0000481"}


id: PBO:0054810
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 2223","termid":"PBO:0054810"}


id: PBO:0050490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox B cluster","termid":"PBO:0050490"}


id: PBO:0084148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-affinity maltose transporter; narrow substrate specificity, transporting maltose and turanose but not other alpha-glucosides; other names include alpha-glucoside transporter and maltose permease","termid":"PBO:0084148"}


id: PBO:0073548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 and multiple ankyrin repeat domains 2","termid":"PBO:0073548"}


id: PBO:0116759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMARCE1 pseudogene 5","termid":"PBO:0116759"}


id: GO:0102243
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E,10E)-geranylgeraniol + ATP = (2E,6E,10E)-geranylgeranyl phosphate + ADP + H+.","definition_xrefs":["RHEA:61664"],"direct_ancestors":[{"relation_name":"is_a","term_name":"geranylgeraniol kinase activity","termid":"GO:0052671"}],"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:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"ATP:geranylgeraniol kinase activity","secondary_identifiers":["MetaCyc:RXN-12325"],"synonyms":[{"name":"ATP:geranylgeraniol phosphotransferase activity","type":"exact"}],"termid":"GO:0102243"}


id: PBO:0042017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 74A","termid":"PBO:0042017"}


id: PBO:0079687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin family domain containing 1 pseudogene 1","termid":"PBO:0079687"}


id: GO:0075206
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism activates, maintains or increases the frequency, rate or extent of cAMP-mediated signal transduction in the symbiont organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by host of symbiont cAMP-mediated signal transduction (obsolete GO:0075206)","synonyms":[{"name":"positive regulation by host of symbiont cAMP-mediated signaling","type":"exact"}],"termid":"GO:0075206"}


id: SO:0000401
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute describing a gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"feature_attribute","termid":"SO:0000733"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene_attribute","synonyms":[{"name":"gene attribute","type":"exact"}],"termid":"SO:0000401"}


id: PBO:0042170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cellular communication network factor 1","termid":"PBO:0042170"}


id: GO:0002105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Endonucleolytic cleavage between the LSU-rRNA and the 4.5S rRNA of an rRNA molecule originally produced as a tetracistronic rRNA transcript that contains the Small Subunit (SSU) rRNA, Large Subunit (LSU) the 4.5S rRNA, and the 5S rRNA in that order from 5' to 3' along the primary transcript. Note that the use of the word tetracistronic refers only to the number of mature rRNA molecules which will be produced from the primary transcript and ignores tRNAs that may also be present within the primary transcript.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endonucleolytic cleavage of tetracistronic rRNA transcript (SSU-rRNA, LSU-rRNA, 4.5S-rRNA, 5S-rRNA)","termid":"GO:0002103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0044085","GO:0010467","GO:0008150","GO:0042254"],"is_obsolete":false,"name":"endonucleolytic cleaveage between LSU-rRNA and 4.5S rRNA of tetracistronic rRNA transcript (SSU-rRNA, LSU-rRNA, 4.5S-rRNA, 5S-rRNA)","termid":"GO:0002105"}


id: MONDO:0002772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the ventricles of the brain.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"cerebral meningioma","termid":"MONDO:0003772"},{"relation_name":"is_a","term_name":"cerebral ventricle cancer","termid":"MONDO:0002682"},{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"},{"relation_name":"is_a","term_name":"malignant tumor of meninges","termid":"MONDO:0021322"}],"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":"intraventricular meningioma","secondary_identifiers":["UMLS:C1334271","MEDGEN:232669","NCIT:C5273","DOID:3772"],"synonyms":[{"name":"brain ventricle meningioma (disease)","type":"exact"},{"name":"meningioma (disease) of brain ventricle","type":"exact"}],"termid":"MONDO:0002772","xrefs":{"Monarch":{"xref_id":"0002772"}}}


id: MONDO:0016092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Serous or mucinous cystadenoma of childhood is a benign epithelial ovarian tumor characterized by a usually unilateral, cystic, unilocular or multilocular lesion with a thin wall or septa and no intracystic solid portion on imaging. It often presents with abdominal pain or an asymptomatic abdominal mass and can be associated with ovarian torsion or malignant transformation.","definition_xrefs":["Orphanet:206470"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian benign neoplasm","termid":"MONDO:0000646"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serous or mucinous cystadenoma of childhood","secondary_identifiers":["MEDGEN:1803886","UMLS:C5679785","GARD:20346"],"synonyms":[{"name":"mucinous cystadenoma of ovary in childhood","type":"exact"},{"name":"serous cystadenoma of ovary in childhood","type":"exact"}],"termid":"MONDO:0016092","xrefs":{"Monarch":{"xref_id":"0016092"}}}


id: PBO:0039161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate kinase 6","termid":"PBO:0039161"}


id: PR:P36209
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sts1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P36209"],"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":"delta(24(24(1)))-sterol reductase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC20G4.07c","synonyms":[{"name":"C-24(28) sterol reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-sts1","type":"exact"},{"name":"sterol Delta(24(28))-reductase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P36209"}


id: GO:1901815
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of astaxanthin.","definition_xrefs":["MetaCyc:PWY-5288","PMID:16434154","UniPathway:UPA00387","GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll biosynthetic process","termid":"GO:0016123"},{"relation_name":"is_a","term_name":"astaxanthin metabolic process","termid":"GO:1901813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"astaxanthin biosynthetic process","synonyms":[{"name":"astaxanthin anabolism","type":"exact"},{"name":"astaxanthin biosynthesis","type":"exact"},{"name":"astaxanthin formation","type":"exact"},{"name":"astaxanthin synthesis","type":"exact"}],"termid":"GO:1901815"}


id: FYPO:0003904
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, or structure of the plasma membrane 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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal plasma membrane morphology","synonyms":[{"name":"normal plasma membrane morphology during mitotic cell cycle","type":"related"},{"name":"normal plasma membrane morphology during vegetative growth","type":"exact"}],"termid":"FYPO:0003904"}


id: PBO:0061107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family CARD domain containing 5","termid":"PBO:0061107"}


id: SO:0001950
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 4th residue (a lysine), from the start of the H4 protein is tri-methylated.","definition_xrefs":["EBI:nj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_methylation_site","termid":"SO:0001701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"H4K4_trimethylation_site","synonyms":[{"name":" H4K4me3","type":"exact"},{"name":"H4K4 trimethylation site","type":"exact"}],"termid":"SO:0001950"}


id: MONDO:0009678
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fukuyama type muscular dystrophy (FCMD) is a congenital progressive muscular dystrophy characterized by brain malformation (cobblestone lissencephaly), dystrophic changes in skeletal muscle, severe intellectual deficit, epilepsy and motor impairment.","definition_xrefs":["Orphanet:272"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type A","termid":"MONDO:0000171"},{"relation_name":"is_a","term_name":"muscle-eye-brain disease","termid":"MONDO:0018939"},{"relation_name":"is_a","term_name":"myopathy caused by variation in FKTN","termid":"MONDO:0700067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322","MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4","secondary_identifiers":["NANDO:2200860","NORD:1169","UMLS:C0410174","OMIM:253800","NCIT:C126741","NANDO:1200494","GARD:6475","MEDGEN:140820","SCTID:111502003","DOID:0050559"],"synonyms":[{"name":"FCMD","type":"exact"},{"name":"Fukuyama Type Congenital Muscular Dystrophy","type":"exact"},{"name":"Fukuyama congenital muscular dystrophy","type":"exact"},{"name":"MDDGA4","type":"exact"},{"name":"Walker-Warburg syndrome or muscle-eye-brain disease, FKTN-related","type":"exact"},{"name":"congenital muscular dystrophy, Fukuyama type","type":"related"},{"name":"muscle-eye-brain-FKTN related","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with Brain and eye anomalies) type A, 4","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4","type":"exact"}],"termid":"MONDO:0009678","xrefs":{"Monarch":{"xref_id":"0009678"}}}


id: PBO:0064227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase C gamma 1","termid":"PBO:0064227"}


id: GO:0071163
data:
  {"annotated_genes":["SJAG_04879","SJAG_01823","SJAG_04995","SJAG_00327","SJAG_02607","SJAG_02908","SJAG_02667"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110266,113895,107666,115735],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140529"},{"annotations":[72376,78513,57521],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902977"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form the DNA replication preinitiation complex, a protein-DNA complex that is assembled at DNA replication origins as part of initiation of DNA replication. The complex consists of proteins that initiate the DNA binding, melt the helix and enable helicase activity.","definition_xrefs":["PMID:28209641","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"is_a","term_name":"protein-DNA complex assembly","termid":"GO:0065004"},{"relation_name":"part_of","term_name":"nuclear DNA replication","termid":"GO:0033260"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00327":null,"SJAG_01823":null,"SJAG_02607":null,"SJAG_02667":null,"SJAG_02908":null,"SJAG_04879":null,"SJAG_04995":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0065003","GO:0006259","GO:0044085","GO:0008150","GO:0006260","GO:0007049"],"is_obsolete":false,"name":"DNA replication preinitiation complex assembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:1902316","GO:1902293"],"synonyms":[{"name":"DNA replication preinitiation complex formation","type":"exact"},{"name":"pre-IC complex assembly","type":"exact"}],"termid":"GO:0071163","terms_by_termid":{"GO:0140529":null,"GO:1902977":null}}


id: PBO:0002900
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.-.-.-","termid":"PBO:0002900"}


id: GO:0071358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a type III interferon stimulus. Interferon lambda is the only member of the type III interferon found so far.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to type III interferon","termid":"GO:0034342"},{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to type III interferon","synonyms":[{"name":"cellular response to interferon-lambda","type":"narrow"},{"name":"cellular response to type III IFN","type":"exact"}],"termid":"GO:0071358"}


id: PBO:0062824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-sialoglycoprotein endopeptidase like 1","termid":"PBO:0062824"}


id: MONDO:0005948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Ritter disease (obsolete MONDO:0005948)","termid":"MONDO:0005948","xrefs":{"Monarch":{"xref_id":"0005948"}}}


id: SO:0000062
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An intrachromosomal transposition whereby a translocation in which one of the four broken ends loses a segment before re-joining.","definition_xrefs":["FB:reference_manual"],"direct_ancestors":[{"relation_name":"has_part","term_name":"deletion","termid":"SO:0000159"},{"relation_name":"is_a","term_name":"chromosomal_deletion","termid":"SO:1000029"},{"relation_name":"is_a","term_name":"intrachromosomal_transposition","termid":"SO:1000041"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deficient_intrachromosomal_transposition","synonyms":[{"name":"deficient intrachromosomal transposition","type":"exact"}],"termid":"SO:0000062"}


id: MONDO:0003398
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Loss of the ability to form new memories beyond a certain point in time. This condition may be organic or psychogenic in origin. Organically induced anterograde amnesia may follow craniocerebral trauma; seizures; anoxia; and other conditions which adversely affect neural structures associated with memory formation (e.g., the hippocampus; fornix (brain); mammillary bodies; and anterior thalamic nuclei). (From Memory 1997 Jan-Mar;5(1-2):49-71)","definition_xrefs":["MESH:D020324"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amnestic disorder","termid":"MONDO:0001152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039"],"is_obsolete":false,"name":"anterograde amnesia","secondary_identifiers":["ICD10CM:R41.1","UMLS:C0233795","icd11.foundation:661071789","MEDGEN:115938","DOID:5340"],"termid":"MONDO:0003398","xrefs":{"Monarch":{"xref_id":"0003398"}}}


id: PR:Q9P3U8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dbl5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P3U8"],"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 RING finger protein C548.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC548.05c","synonyms":[{"name":"Spom972h-dbl5","type":"exact"}],"termid":"PR:Q9P3U8"}


id: PBO:0059151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGUK p55 scaffold protein 3","termid":"PBO:0059151"}


id: MONDO:0008725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital lipoid adrenal hyperplasia (CLAH) is one of the most severe forms of congenital adrenal hyperplasia (CAH) characterized by severe adrenal insufficiency and sex reversal in males.","definition_xrefs":["Orphanet:90790"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital adrenal hyperplasia","termid":"MONDO:0018479"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005047","MONDO:0005066"],"is_obsolete":false,"name":"congenital lipoid adrenal hyperplasia due to STAR deficency","secondary_identifiers":["SCTID:44231009","UMLS:C0342474","MEDGEN:83341","GARD:1465","OMIM:201710"],"synonyms":[{"name":"CLAH","type":"exact"},{"name":"LCAH","type":"related"},{"name":"adrenal hyperplasia 1","type":"related"},{"name":"congenital adrenal hyperplasia lipoid","type":"related"},{"name":"lipoid adrenal hyperplasia","type":"exact"},{"name":"lipoid congenital adrenal hyperplasia","type":"related"},{"name":"lipoid hyperplasia, congenital, of adrenal cortex with Male pseudohermaphroditism","type":"related"}],"termid":"MONDO:0008725","xrefs":{"Monarch":{"xref_id":"0008725"}}}


id: MONDO:0850284
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic asthma that is triggered by an allergen and that is characterized by an immune system overreaction to a harmless substance, such as pollen or dust, with the subsequent release of immunoglobin E (IgE) antibodies.","definition_xrefs":["DOID:0080811"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic asthma","termid":"MONDO:0850282"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extrinsic asthma","termid":"MONDO:0850284","xrefs":{"Monarch":{"xref_id":"0850284"}}}


id: PBO:0070889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15 pseudogene 21","termid":"PBO:0070889"}


id: PBO:0027050
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_H2A_phosphorylation_during_cellular_response_to_ionizing_radiation","termid":"PBO:0027050"}


id: MONDO:1010570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes insipidus that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"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, pig","secondary_identifiers":["OMIA:000278-9823"],"termid":"MONDO:1010570","xrefs":{"Monarch":{"xref_id":"1010570"}}}


id: PR:Q09813
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- taf111 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09813"],"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":"transcription initiation factor TFIID 111 kDa subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2G11.14","synonyms":[{"name":"Spom972h-taf111","type":"exact"},{"name":"TAFII-111 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"TBP-associated factor 111 kDa (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09813"}


id: MONDO:0001802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"tympanitis","termid":"MONDO:0024616"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute tympanitis","secondary_identifiers":["SCTID:297009","DOID:13790","UMLS:C0155460","ICD9:384.00","MEDGEN:509976"],"synonyms":[{"name":"acute myringitis","type":"exact"}],"termid":"MONDO:0001802","xrefs":{"Monarch":{"xref_id":"0001802"}}}


id: GO:1901415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of tetrapyrrole biosynthetic process from glycine and succinyl-CoA.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of amide metabolic process","termid":"GO:0034250"},{"relation_name":"is_a","term_name":"positive regulation of amino acid metabolic process","termid":"GO:0045764"},{"relation_name":"is_a","term_name":"positive regulation of nucleobase-containing compound metabolic process","termid":"GO:0045935"},{"relation_name":"is_a","term_name":"positive regulation of phosphate metabolic process","termid":"GO:0045937"},{"relation_name":"is_a","term_name":"positive regulation of sulfur metabolic process","termid":"GO:0051176"},{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"is_a","term_name":"regulation of tetrapyrrole biosynthetic process from glycine and succinyl-CoA","termid":"GO:1901413"},{"relation_name":"is_a","term_name":"positive regulation of tetrapyrrole biosynthetic process","termid":"GO:1901465"},{"relation_name":"positively_regulates","term_name":"tetrapyrrole biosynthetic process from glycine and succinyl-CoA","termid":"GO:0033527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006790"},{"rel_name":"positively_regulates","termid":"GO:0033013"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0055086"},{"rel_name":"positively_regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0033013"},{"rel_name":"regulates","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0033013","GO:0044281","GO:0055086","GO:0006790","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"positive regulation of tetrapyrrole biosynthetic process from glycine and succinyl-CoA","synonyms":[{"name":"activation of tetrapyrrole anabolism from glycine and succinyl-CoA","type":"exact"},{"name":"activation of tetrapyrrole biosynthesis from glycine and succinyl-CoA","type":"exact"},{"name":"activation of tetrapyrrole biosynthetic process from glycine and succinyl-CoA","type":"narrow"},{"name":"activation of tetrapyrrole formation from glycine and succinyl-CoA","type":"exact"},{"name":"activation of tetrapyrrole synthesis from glycine and succinyl-CoA","type":"exact"},{"name":"positive regulation of tetrapyrrole anabolism from glycine and succinyl-CoA","type":"exact"},{"name":"positive regulation of tetrapyrrole biosynthesis from glycine and succinyl-CoA","type":"exact"},{"name":"positive regulation of tetrapyrrole formation from glycine and succinyl-CoA","type":"exact"},{"name":"positive regulation of tetrapyrrole synthesis from glycine and succinyl-CoA","type":"exact"},{"name":"up regulation of tetrapyrrole anabolism from glycine and succinyl-CoA","type":"exact"},{"name":"up regulation of tetrapyrrole biosynthesis from glycine and succinyl-CoA","type":"exact"},{"name":"up regulation of tetrapyrrole biosynthetic process from glycine and succinyl-CoA","type":"exact"},{"name":"up regulation of tetrapyrrole formation from glycine and succinyl-CoA","type":"exact"},{"name":"up regulation of tetrapyrrole synthesis from glycine and succinyl-CoA","type":"exact"},{"name":"up-regulation of tetrapyrrole anabolism from glycine and succinyl-CoA","type":"exact"},{"name":"up-regulation of tetrapyrrole biosynthesis from glycine and succinyl-CoA","type":"exact"},{"name":"up-regulation of tetrapyrrole biosynthetic process from glycine and succinyl-CoA","type":"exact"},{"name":"up-regulation of tetrapyrrole formation from glycine and succinyl-CoA","type":"exact"},{"name":"up-regulation of tetrapyrrole synthesis from glycine and succinyl-CoA","type":"exact"},{"name":"upregulation of tetrapyrrole anabolism from glycine and succinyl-CoA","type":"exact"},{"name":"upregulation of tetrapyrrole biosynthesis from glycine and succinyl-CoA","type":"exact"},{"name":"upregulation of tetrapyrrole biosynthetic process from glycine and succinyl-CoA","type":"exact"},{"name":"upregulation of tetrapyrrole formation from glycine and succinyl-CoA","type":"exact"},{"name":"upregulation of tetrapyrrole synthesis from glycine and succinyl-CoA","type":"exact"}],"termid":"GO:1901415"}


id: MONDO:0002380
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant tumor characterized by the presence of cells that show myoepithelial differentiation. Based on its morphologic features, it is classified as benign or malignant. A representative example of benign myoepithelioma is benign salivary gland myoepithelioma. Representative examples of malignant myoepithelioma or myoepithelial carcinoma are malignant breast myoepithelioma and salivary gland myoepithelial carcinoma.","definition_xrefs":["NCIT:C40392"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myoepithelial tumor","secondary_identifiers":["UMLS:C0027070","ICDO:8982/0","DOID:2661","MEDGEN:10235","ICDO:8982/1","MESH:D009208"],"synonyms":[{"name":"benign myoepithelioma","type":"narrow"},{"name":"myoepithelial adenoma","type":"exact"},{"name":"myoepithelial neoplasm","type":"exact"},{"name":"myoepithelial tumor","type":"exact"},{"name":"myoepithelioma","type":"exact"}],"termid":"MONDO:0002380","xrefs":{"Monarch":{"xref_id":"0002380"}}}


id: PBO:0069302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 558, pseudogene","termid":"PBO:0069302"}


id: PBO:0062238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily BB member 1 pseudogene","termid":"PBO:0062238"}


id: MONDO:0009764
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ocular motor apraxia, Cogan type is characterized by impairment of voluntary horizontal eye movements and compensatory head thrust. Around 50 cases have been described so far. The oculomotor manifestations tend to improve with age but the syndrome may also be associated with learning and speech difficulties, or, in some cases, cerebral malformations. Both sporadic and familial forms have been described, with sporadic forms being more frequent. The mode of transmission of the familial form has not yet been clearly established. A gene located on the long arm of chromosome 2, near to the NPHP1 gene involved in nephronophthisis, may be associated with ocular motor apraxia, Cogan type.","definition_xrefs":["Orphanet:1125"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"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":"ocular motor apraxia, Cogan type","secondary_identifiers":["SCTID:405809000","NORD:1517","OMIM:257550","MEDGEN:154254","GARD:16","MESH:C537423","DOID:0080849","UMLS:C0543874"],"synonyms":[{"name":"COMA","type":"related"},{"name":"Cogan syndrome type 2","type":"related"},{"name":"Cogan's syndrome type 2","type":"related"},{"name":"congenital oculomotor apraxia","type":"related"},{"name":"ocular motor apraxia","type":"related"},{"name":"oculomotor apraxia Cogan type","type":"related"},{"name":"oculomotor apraxia, Cogan type","type":"exact"},{"name":"oculomotor apraxia, congenital, Cogan-type","type":"exact"},{"name":"saccade initiation failure congenital","type":"related"},{"name":"saccade initiation failure, congenital","type":"related"}],"termid":"MONDO:0009764","xrefs":{"Monarch":{"xref_id":"0009764"}}}


id: MONDO:0005913
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Influenza-like febrile viral disease caused by several members of the bunyaviridae family and transmitted mostly by the bloodsucking sandfly Phlebotomus papatasii.","definition_xrefs":["MESH:D010217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"},{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phlebotomus fever","secondary_identifiers":["SCTID:407476002","UMLS:C0030372","ICD9:066.0","DOID:11360","EFO:0007437","ICD10CM:A93.1","MEDGEN:14597"],"synonyms":[{"name":"Sandfly fever","type":"exact"},{"name":"Sandfly-borne Bunyavirus fever","type":"exact"},{"name":"Sandfly-borne arboviral fever","type":"exact"},{"name":"Sandfly-borne phleboviral disease","type":"exact"},{"name":"pappataci fever","type":"exact"}],"termid":"MONDO:0005913","xrefs":{"Monarch":{"xref_id":"0005913"}}}


id: PBO:0117395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease P/MRP subunit p25","termid":"PBO:0117395"}


id: PBO:0084540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the p24 family involved in ER to Golgi transport; similar to Emp24p and Erv25p; ERP4 has a paralog, ERP2, that arose from the whole genome duplication","termid":"PBO:0084540"}


id: PBO:0076095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntaxin 1B","termid":"PBO:0076095"}


id: GO:0047209
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: coniferyl alcohol + UDP-D-glucose = coniferin + UDP.","definition_xrefs":["MetaCyc:2.4.1.111-RXN","EC:2.4.1.111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016757","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"coniferyl-alcohol glucosyltransferase activity","secondary_identifiers":["RHEA:23944"],"synonyms":[{"name":"UDP-glucose coniferyl alcohol glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:coniferyl-alcohol 4'-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:coniferyl-alcohol 4'-beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-coniferyl alcohol glucosyltransferase activity","type":"related"}],"termid":"GO:0047209"}


id: PR:O14120
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mvp1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14120"],"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":"sorting nexin mvp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A11.06","synonyms":[{"name":"Spom972h-mvp1","type":"exact"}],"termid":"PR:O14120"}


id: PBO:0060105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 6","termid":"PBO:0060105"}


id: MOD:01713
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue hydroxyl with one of the Applied Biosystems iTRAQ4plex reagent reporter+balance acyloxy groups.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isotope tagged reagent O-acylated residue","termid":"MOD:01707"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ4plex reporter+balance reagent O-acylated residue","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"}],"termid":"MOD:01713"}


id: PBO:0049454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucoside xylosyltransferase 2","termid":"PBO:0049454"}


id: SO:0000044
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A pseudogene caused by unequal crossing over at recombination.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_processed_pseudogene","termid":"SO:0001760"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudogene_by_unequal_crossing_over","synonyms":[{"name":"pseudogene by unequal crossing over","type":"exact"}],"termid":"SO:0000044"}


id: GO:0010693
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of alkaline phosphatase activity, the catalysis of the reaction: an orthophosphoric monoester + H2O = an alcohol + phosphate, with an alkaline pH optimum.","definition_xrefs":["GOC:dph","GOC:BHF","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of alkaline phosphatase activity","termid":"GO:0010692"},{"relation_name":"is_a","term_name":"negative regulation of phosphatase activity","termid":"GO:0010923"}],"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 alkaline phosphatase activity","termid":"GO:0010693"}


id: MOD:00502
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes three hydrogen atoms of a residue with three iodine atoms.","definition_xrefs":["PubMed:2026710","PubMed:15627961","Unimod:131","OMSSA:116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iodinated residue","termid":"MOD:00755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triiodinated residue","synonyms":[{"name":"I3Res","type":"exact"},{"name":"Triiodo","type":"related"},{"name":"tri-Iodination","type":"related"},{"name":"triiodinationy","type":"exact"}],"termid":"MOD:00502"}


id: MONDO:0006626
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic, pathological complication associated with diabetes mellitus, where nerve damages are incurred due to diabetic microvascular injury involving small blood vessels that supply these nerves, resulting in peripheral and/or autonomic nerve dysfunction.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral neuropathy","termid":"MONDO:0005244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"diabetic neuropathy","secondary_identifiers":["MEDGEN:8353","EFO:1000783","UMLS:C0011882","DOID:9743","MESH:D003929","ICD9:250.6","SCTID:230572002","NCIT:C26748"],"termid":"MONDO:0006626","xrefs":{"Monarch":{"xref_id":"0006626"}}}


id: GO:0007282
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any of the rounds of incomplete mitosis undergone by a cystoblast to form a cyst of interconnected cells.","definition_xrefs":["PMID:21452446"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asymmetric cell division","termid":"GO:0008356"},{"relation_name":"part_of","term_name":"germ cell development","termid":"GO:0007281"}],"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":"cystoblast division","synonyms":[{"name":"cystoblast cell division","type":"exact"}],"termid":"GO:0007282"}


id: PBO:0040978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein like","termid":"PBO:0040978"}


id: PATO:0001558
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of a process inhering in a bearer by virtue of the bearer's lacking a processual part as specified by the additional entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extra or missing processual parts","termid":"PATO:0001564"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lacking processual parts","termid":"PATO:0001558"}


id: PBO:0050750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family E (Hsp10) member 1 pseudogene 12","termid":"PBO:0050750"}


id: GO:0047139
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: homocystine + 2 reduced glutathione = oxidized glutathione + 2 homocysteine.","definition_xrefs":["MetaCyc:1.8.4.1-RXN","EC:1.8.4.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor","termid":"GO:0016671"}],"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:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"glutathione-homocystine transhydrogenase activity","secondary_identifiers":["RHEA:11464"],"synonyms":[{"name":"glutathione:homocystine oxidoreductase activity","type":"related"}],"termid":"GO:0047139"}


id: PR:O43023
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transferrin receptor protein 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02508","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":"inactive zinc metalloprotease C354.09c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC354.09c","secondary_identifiers":["UniProtKB:O43023"],"synonyms":[{"name":"Spom972h-TFR2","type":"exact"}],"termid":"PR:O43023"}


id: PBO:0005764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridoxamine/pyridoxine/pyridoxal transmembrane transporter (predicted)","termid":"PBO:0005764"}


id: PBO:0052425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KiSS-1 metastasis suppressor","termid":"PBO:0052425"}


id: GO:0070661
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of a leukocyte population by cell division.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population proliferation","termid":"GO:0008283"}],"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":"leukocyte proliferation","termid":"GO:0070661"}


id: PBO:0031276
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_negative_regulation_of_G0_to_G1_transition","termid":"PBO:0031276"}


id: GO:0140708
data:
  {"annotated_genes":["SJAG_01074"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114740],"is_not":false,"summary":null,"term":"GO:0140708"}]},"cv_name":"biological_process","definition":"The C-terminal elongation of 60S-anchored stalled nascent polypeptide chains with untemplated alanine and threonine tails (CAT tails). CAT tails participate in the recognition of stalled nascent chains by the ribosome quality control system.","definition_xrefs":["PMID:32934225","PMID:25554787"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic translational elongation","termid":"GO:0002182"},{"relation_name":"part_of","term_name":"rescue of stalled ribosome","termid":"GO:0072344"},{"relation_name":"part_of","term_name":"ribosome-associated ubiquitin-dependent protein catabolic process","termid":"GO:1990116"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01074":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0002181"},{"rel_name":"part_of","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0030163","GO:0010467","GO:0002181"],"is_obsolete":false,"name":"CAT tailing","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140708","terms_by_termid":{"GO:0140708":null}}


id: GO:0075257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of teliospore formation, which is the formation of a thick-walled resting or overwintering spore produced by the rust fungi (Uredinales) and smut fungi (Ustilaginales) in which karyogamy occurs.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043945"},{"relation_name":"is_a","term_name":"regulation of teliospore formation","termid":"GO:0075256"},{"relation_name":"positively_regulates","term_name":"teliospore formation","termid":"GO:0075255"}],"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 teliospore formation","termid":"GO:0075257"}


id: PBO:0018216
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-related_via_dependence_to","termid":"PBO:0018216"}


id: PBO:0027324
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitochondria_present_in_normal_numbers","termid":"PBO:0027324"}


id: PBO:0028415
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_frequency_of_meiosis_I","termid":"PBO:0028415"}


id: PBO:0054954
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 2368","termid":"PBO:0054954"}


id: PR:P40234
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cki2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P40234"],"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":"casein kinase I homolog 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP35G2.05c","synonyms":[{"name":"Spom972h-cki2","type":"exact"}],"termid":"PR:P40234"}


id: PBO:0069265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 521, pseudogene","termid":"PBO:0069265"}


id: MONDO:0018471
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Generalized eruptive keratoacanthoma (GEKA) is rare variant of keratoacanthoma (KA) that affects the skin and mucous membranes and which is characterized by a sudden generalized eruption of severely pruritic, hundreds to thousands of small follicular papules, often with a central keratotic plug.","definition_xrefs":["Orphanet:411777"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"is_a","term_name":"keratoacanthoma","termid":"MONDO:0002527"}],"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":"generalized eruptive keratoacanthoma","secondary_identifiers":["GARD:21736","UMLS:C0345985","SCTID:254664008","MEDGEN:577226"],"synonyms":[{"name":"GEKA","type":"exact"},{"name":"Grzybowski syndrome","type":"exact"},{"name":"generalised eruptive keratoacanthomas of Grzybowski","type":"exact"},{"name":"generalized eruptive keratoacanthomas of Grzybowski","type":"exact"}],"termid":"MONDO:0018471","xrefs":{"Monarch":{"xref_id":"0018471"}}}


id: GO:2000392
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lamellipodium morphogenesis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell morphogenesis","termid":"GO:0022604"},{"relation_name":"is_a","term_name":"regulation of lamellipodium organization","termid":"GO:1902743"},{"relation_name":"regulates","term_name":"lamellipodium morphogenesis","termid":"GO:0072673"}],"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 lamellipodium morphogenesis","synonyms":[{"name":"regulation of lamellipodium organization","type":"related"}],"termid":"GO:2000392"}


id: PBO:0054546
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 1946","termid":"PBO:0054546"}


id: PBO:0056890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MID1 interacting protein 1","termid":"PBO:0056890"}


id: PBO:0004519
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.5.4.12","termid":"PBO:0004519"}


id: MONDO:0002213
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tularemia (obsolete MONDO:0002213)","termid":"MONDO:0002213","xrefs":{"Monarch":{"xref_id":"0002213"}}}


id: GO:0061906
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an autophagosome is transported to, and/or maintained in, a specific location within the cell.","definition_xrefs":["PMID:26763909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuolar localization","termid":"GO:1990849"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"autophagosome localization","termid":"GO:0061906"}


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


id: PBO:0090262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L4","termid":"PBO:0090262"}


id: PBO:0053431
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 376","termid":"PBO:0053431"}


id: MONDO:0018228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bipartite talus is a rare, genetic bone disorder characterized by the presence of two non-fused talar bone fragments, with the posterior fragment located at the level of the posterior talar process. Patients may present with foot and/or ankle pain (exercise-induced or not), repetitive ankle sprains, chronic ankle ligamentous laxity, restricted ankle motion (i.e. plantar flexion, eversion, and inversion), and mild swelling.","definition_xrefs":["Orphanet:364198"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"}],"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":"bipartite talus","secondary_identifiers":["MEDGEN:1631166","UMLS:C4706298","SCTID:763128009","GARD:21566"],"termid":"MONDO:0018228","xrefs":{"Monarch":{"xref_id":"0018228"}}}


id: GO:0061604
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: [Molybdopterin-synthase sulfur-carrier protein]-Gly-Gly-AMP + [cysteine desulfurase]-S-sulfanyl-L-cysteine = AMP [molybdopterin-synthase sulfur-carrier protein]-Gly-NH-CH(2)-C(O)SH + cysteine desulfurase.","definition_xrefs":["PMID:18154309","EC:2.8.1.11","PMID:22370186","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfurtransferase activity","termid":"GO:0016783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016782","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"molybdopterin-synthase sulfurtransferase activity","secondary_identifiers":["RHEA:48612"],"termid":"GO:0061604"}


id: PBO:0039268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALDOA pseudogene 1","termid":"PBO:0039268"}


id: MONDO:1012538
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital dyserythropoietic anemia, non-human animal","termid":"MONDO:1011707"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital dyserythropoietic anemia, cattle","secondary_identifiers":["OMIA:002300-9913"],"termid":"MONDO:1012538","xrefs":{"Monarch":{"xref_id":"1012538"}}}


id: PBO:0050275
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 5","termid":"PBO:0050275"}


id: PBO:0075946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stromal antigen 3-like 1 (pseudogene)","termid":"PBO:0075946"}


id: PBO:0070118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 32 pseudogene","termid":"PBO:0070118"}


id: PBO:0062077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily A member 8 (gene/pseudogene)","termid":"PBO:0062077"}


id: GO:0007447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process that results in defined areas of the imaginal disc that will undergo specific cell differentaiton. Imaginal discs are epithelial infoldings in the larvae of holometabolous insects that develop into adult appendages (legs, antennae, wings, etc.) during metamorphosis from larval to adult form.","definition_xrefs":["GOC:jid","GOC:dph","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"part_of","term_name":"imaginal disc development","termid":"GO:0007444"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"imaginal disc pattern formation","termid":"GO:0007447"}


id: MONDO:0020150
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete obsolete rare palpebral, lacrimal system and conjunctival disease (obsolete MONDO:0020150)","secondary_identifiers":["Orphanet:98559"],"termid":"MONDO:0020150","xrefs":{"Monarch":{"xref_id":"0020150"}}}


id: PBO:0068296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 2 pseudogene 1","termid":"PBO:0068296"}


id: MONDO:0000905
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cortisone reductase deficiency (obsolete MONDO:0000905)","termid":"MONDO:0000905","xrefs":{"Monarch":{"xref_id":"0000905"}}}


id: GO:0016858
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Racemase and epimerase activity on compounds other than amino acids, hydroxy acids, carbohydrates or their derivatives.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete racemase and epimerase activity, acting on other compounds (obsolete GO:0016858)","synonyms":[{"name":"racemase and epimerase activity, acting on other compounds","type":"exact"}],"termid":"GO:0016858"}


id: GO:0036171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a group of unicellular organisms grow in a threadlike, filamentous shape in response to a chemical stimulus.","definition_xrefs":["PMID:17554048","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"filamentous growth of a population of unicellular organisms","termid":"GO:0044182"},{"relation_name":"part_of","term_name":"response to chemical","termid":"GO:0042221"}],"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":"filamentous growth of a population of unicellular organisms in response to chemical stimulus","termid":"GO:0036171"}


id: PBO:0090783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, serine Fsf1","termid":"PBO:0090783"}


id: PBO:0064699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 35","termid":"PBO:0064699"}


id: MONDO:0012818
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any maturity-onset diabetes of the young in which the cause of the disease is a mutation in the PAX4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maturity-onset diabetes of the young","termid":"MONDO:0018911"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005015"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005015","MONDO:0037792","MONDO:0004335","MONDO:0019254"],"is_obsolete":false,"name":"maturity-onset diabetes of the young type 9","secondary_identifiers":["DOID:0111107","MEDGEN:383033","UMLS:C2677132","MESH:C567393","SCTID:609576002","GARD:10663","OMIM:612225"],"synonyms":[{"name":"MODY PAX4 related","type":"related"},{"name":"MODY type 9","type":"related"},{"name":"MODY9","type":"exact"},{"name":"PAX4 maturity-onset diabetes of the young (disease)","type":"exact"},{"name":"diabetes mellitus MODY type 9","type":"related"},{"name":"maturity-onset diabetes of the young (disease) caused by mutation in PAX4","type":"exact"},{"name":"maturity-onset diabetes of the young, type 9","type":"related"},{"name":"maturity-onset diabetes of the young, type IX","type":"exact"},{"name":"type 9 maturity-onset diabetes of the young","type":"related"}],"termid":"MONDO:0012818","xrefs":{"Monarch":{"xref_id":"0012818"}}}


id: MONDO:0008507
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":"surface polypeptides, anonymous","secondary_identifiers":["MEDGEN:348354","UMLS:C1861417","OMIM:185610"],"synonyms":[{"name":"Spa2","type":"related"},{"name":"Spa5","type":"related"},{"name":"surface polypeptides, anonymous","type":"exact"}],"termid":"MONDO:0008507","xrefs":{"Monarch":{"xref_id":"0008507"}}}


id: PBO:0075622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sprouty related EVH1 domain containing 3","termid":"PBO:0075622"}


id: PR:C6Y4C6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC29A10.17 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4C6"],"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 C29A10.17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29A10.17","synonyms":[{"name":"Spom972h-SPBC29A10.17","type":"exact"}],"termid":"PR:C6Y4C6"}


id: MOD:01445
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to L-3,3-dihydroxyoalanine.","definition_xrefs":["RESID:AA0492#SER","PubMed:17558559","PubMed:11435113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"},{"relation_name":"is_a","term_name":"L-3,3-dihydroxyoalanine","termid":"MOD:01448"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-3,3-dihydroxyoalanine (Ser)","synonyms":[{"name":"(S)-2-amino-3,3-dihydroxypropanoic acid","type":"exact"},{"name":"2-(dihydroxymethyl)glycine","type":"exact"},{"name":"3,3-dihydroxy-L-alanine","type":"exact"},{"name":"3,3-dihydroxyalanine","type":"exact"},{"name":"3-hydroxy-L-serine","type":"exact"},{"name":"3-oxoalanine hydrate","type":"exact"},{"name":"C(alpha)-formylglycine hydrate","type":"related"}],"termid":"MOD:01445"}


id: GO:0001533
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A type of plasma membrane that has been modified through addition of distinct intracellular and extracellular components, including ceramide, found in cornifying epithelial cells (corneocytes).","definition_xrefs":["PMID:11590230","PMID:15803139","PMID:11112355","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane","termid":"GO:0005886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"cornified envelope","termid":"GO:0001533"}


id: PBO:0065738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal membrane protein 2","termid":"PBO:0065738"}


id: PBO:0059906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND1 pseudogene 29","termid":"PBO:0059906"}


id: MONDO:0004986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the urinary bladder","direct_ancestors":[{"relation_name":"is_a","term_name":"urinary bladder cancer","termid":"MONDO:0001187"},{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"urinary bladder carcinoma","secondary_identifiers":["UMLS:C0699885","DOID:4007","NCIT:C4912","SCTID:255108000","HP:0002862","MEDGEN:147071"],"synonyms":[{"name":"bladder cancer","type":"broad"},{"name":"bladder carcinoma","type":"exact"},{"name":"cancer of bladder","type":"broad"},{"name":"cancer of the bladder","type":"broad"},{"name":"cancer of the urinary bladder","type":"broad"},{"name":"cancer of urinary bladder","type":"broad"},{"name":"carcinoma bladder","type":"exact"},{"name":"carcinoma of bladder","type":"exact"},{"name":"carcinoma of the bladder","type":"exact"},{"name":"carcinoma of the urinary bladder","type":"exact"},{"name":"carcinoma of urinary bladder","type":"exact"},{"name":"urinary bladder cancer","type":"broad"},{"name":"urinary bladder carcinoma","type":"exact"}],"termid":"MONDO:0004986","xrefs":{"Monarch":{"xref_id":"0004986"}}}


id: GO:0051961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of nervous system development, the origin and formation of nervous tissue.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of nervous system development","termid":"GO:0051960"},{"relation_name":"negatively_regulates","term_name":"nervous system development","termid":"GO:0007399"}],"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 nervous system development","synonyms":[{"name":"down regulation of nervous system development","type":"exact"},{"name":"down-regulation of nervous system development","type":"exact"},{"name":"downregulation of nervous system development","type":"exact"},{"name":"inhibition of nervous system development","type":"narrow"}],"termid":"GO:0051961"}


id: GO:0160006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An endocytosis process mediated by the Fc receptor for the purpose of delivery of antigen-bound immunoglobulin to an intracellular compartment where the antigen can be processed and loaded onto MHC molecules. This process selectively targets antigens for presentation by MHC class II or cross-presentation by MHC class I.","definition_xrefs":["PMID:9143687","PMID:28389502","PMID:9463401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor-mediated endocytosis","termid":"GO:0006898"},{"relation_name":"is_a","term_name":"protein-containing complex localization","termid":"GO:0031503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"Fc receptor-mediated immune complex endocytosis","synonyms":[{"name":"Fc receptor-mediated immune complex internalization","type":"related"},{"name":"Ig-complexed antigen endocytosis via Fc receptor","type":"exact"},{"name":"antigen-antibody immune complex uptake via Fc receptor","type":"exact"}],"termid":"GO:0160006"}


id: PBO:0050156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 12","termid":"PBO:0050156"}


id: MONDO:0017946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Iowa type is a form of HCHWA characterized by age of onset between 50-66 years of age, memory impairment, myoclonic jerks, expressive dysphagia, short-stepped gait, personality changes and lobar intracerebral hemorrhages.","definition_xrefs":["Orphanet:324708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral amyloid angiopathy, APP-related","termid":"MONDO:0011583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0021179"],"is_obsolete":false,"name":"ABeta amyloidosis, Iowa type","secondary_identifiers":["GARD:17490","ICD10EXP:I68.0*","ICD10EXP:E85.4+","MEDGEN:854855","UMLS:C3888309"],"synonyms":[{"name":"ABetaD23N amyloidosis","type":"exact"},{"name":"HCHWA, Iowa type","type":"exact"},{"name":"cerebral amyloid angiopathy, APP-related, Iowa variant","type":"exact"},{"name":"hereditary cerebral haemorrhage with amyloidosis, Iowa type","type":"exact"},{"name":"hereditary cerebral hemorrhage with amyloidosis, Iowa type","type":"exact"}],"termid":"MONDO:0017946","xrefs":{"Monarch":{"xref_id":"0017946"}}}


id: PBO:0080568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat and FYVE domain containing 3","termid":"PBO:0080568"}


id: PBO:0039136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune regulator","termid":"PBO:0039136"}


id: PBO:0054577
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 1979","termid":"PBO:0054577"}


id: PBO:0076914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor AP-2 beta","termid":"PBO:0076914"}


id: GO:0072540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a CD4-positive, alpha-beta T cell becomes committed to becoming a T-helper 17 cell, a CD4-positive, alpha-beta T cell with the phenotype RORgamma-t-positive that produces IL-17.","definition_xrefs":["GOC:ebc","CL:0000899","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T-helper cell lineage commitment","termid":"GO:0002295"},{"relation_name":"part_of","term_name":"T-helper 17 cell differentiation","termid":"GO:0072539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"T-helper 17 cell lineage commitment","synonyms":[{"name":"T-helper 17 cell fate commitment","type":"exact"},{"name":"Th17 cell lineage commitment","type":"exact"},{"name":"Th17 fate commitment","type":"exact"}],"termid":"GO:0072540"}


id: GO:0036490
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Modulation of the frequency, rate or extent of translation as a result of endoplasmic reticulum stress.","definition_xrefs":["GOC:PARL","PMID:16835242","GOC:bf","PMID:14676213"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation in response to stress","termid":"GO:0043555"},{"relation_name":"part_of","term_name":"response to endoplasmic reticulum stress","termid":"GO:0034976"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of translation in response to endoplasmic reticulum stress","synonyms":[{"name":"regulation of translation in response to ER stress","type":"exact"}],"termid":"GO:0036490"}


id: GO:1902939
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of intracellular calcium activated chloride channel activity.","definition_xrefs":["GO_REF:0000059","GOC:als","PMID:22946059","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of intracellular calcium activated chloride channel activity (obsolete GO:1902939)","synonyms":[{"name":"down regulation of intracellular calcium activated chloride channel activity","type":"exact"},{"name":"down-regulation of intracellular calcium activated chloride channel activity","type":"exact"},{"name":"downregulation of intracellular calcium activated chloride channel activity","type":"exact"},{"name":"inhibition of intracellular calcium activated chloride channel activity","type":"narrow"}],"termid":"GO:1902939"}


id: PBO:0005523
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Coiled Coil protein Quantitatively enriched","termid":"PBO:0005523"}


id: PBO:0081160
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","termid":"PBO:0081160"}


id: PBO:0111822
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HAT repeat protein","termid":"PBO:0111822"}


id: PR:Q9Y7P8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC191.04c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7P8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized membrane protein C191.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC191.04c","synonyms":[{"name":"Spom972h-SPCC191.04c","type":"exact"}],"termid":"PR:Q9Y7P8"}


id: PBO:0086404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative ferric reductase with similarity to Fre2p; expression induced by low iron levels","termid":"PBO:0086404"}


id: MONDO:0010025
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":"short stature-obesity syndrome","secondary_identifiers":["UMLS:C1849235","OMIM:269870","MEDGEN:341410","MESH:C564821"],"synonyms":[{"name":"SSOS","type":"related"},{"name":"short stature-obesity syndrome","type":"exact"}],"termid":"MONDO:0010025","xrefs":{"Monarch":{"xref_id":"0010025"}}}


id: PBO:0080089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 50","termid":"PBO:0080089"}


id: PBO:0054931
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 2345","termid":"PBO:0054931"}


id: GO:0061451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the retrotrapezoid nucleus (RTN) over time from it's initial formation to its mature state. The retrotrapezoid nucleus is a group of neurons in the rostral medulla, which are responsible regulating respiration.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"medulla oblongata development","termid":"GO:0021550"}],"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":"retrotrapezoid nucleus development","termid":"GO:0061451"}


id: PBO:0073517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain binding glutamate rich protein like 2","termid":"PBO:0073517"}


id: PBO:0061805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"outer dense fiber of sperm tails 3 like 1","termid":"PBO:0061805"}


id: GO:0009207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of purine ribonucleoside triphosphate, a compound consisting of a purine base linked to a ribose sugar esterified with triphosphate on the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleoside triphosphate catabolic process","termid":"GO:0009146"},{"relation_name":"is_a","term_name":"ribonucleoside triphosphate catabolic process","termid":"GO:0009203"},{"relation_name":"is_a","term_name":"purine ribonucleoside triphosphate metabolic process","termid":"GO:0009205"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"purine ribonucleoside triphosphate catabolic process","synonyms":[{"name":"purine ribonucleoside triphosphate breakdown","type":"exact"},{"name":"purine ribonucleoside triphosphate catabolism","type":"exact"},{"name":"purine ribonucleoside triphosphate degradation","type":"exact"}],"termid":"GO:0009207"}


id: MONDO:0012440
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"migraine with or without aura, susceptibility to","termid":"MONDO:0100246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"migraine with or without aura, susceptibility to, 10","secondary_identifiers":["UMLS:C1857752","MEDGEN:341839","OMIM:610208"],"synonyms":[{"name":"Mgr10","type":"related"},{"name":"migraine with or without aura, susceptibility to, 10","type":"exact"},{"name":"migraine with or without aura, susceptibility to, type 10","type":"exact"},{"name":"migraine with pulsation","type":"related"}],"termid":"MONDO:0012440","xrefs":{"Monarch":{"xref_id":"0012440"}}}


id: GO:2001308
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the epipolythiodioxopiperazine gliotoxin, a poisonous substance produced by some species of fungi.","definition_xrefs":["PMID:18272357","PMID:16333108","PMID:17574915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"mycotoxin metabolic process","termid":"GO:0043385"},{"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:0006790"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0006790","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"gliotoxin metabolic process","synonyms":[{"name":"gliotoxin metabolism","type":"exact"}],"termid":"GO:2001308"}


id: MONDO:0017438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-syndromic amelia that involves the hindlimb.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic amelia","termid":"MONDO:0017419"}],"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":"amelia of lower limb","secondary_identifiers":["HP:0009818","GARD:21191","SCTID:265798000","icd11.foundation:540310468","UMLS:C0265621","MEDGEN:539370","Orphanet:294969"],"synonyms":[{"name":"hindlimb non-syndromic amelia","type":"exact"},{"name":"non-syndromic amelia of hindlimb","type":"exact"}],"termid":"MONDO:0017438","xrefs":{"Monarch":{"xref_id":"0017438"}}}


id: GO:0002055
data:
  {"annotated_genes":["SJAG_01859"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74278],"is_not":false,"summary":null,"term":"GO:0002055"}]},"cv_name":"molecular_function","definition":"Binding to adenine, a purine base.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleobase binding","termid":"GO:0002060"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01859":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"adenine binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"6-aminopurine binding","type":"exact"}],"termid":"GO:0002055","terms_by_termid":{"GO:0002055":null}}


id: GO:0106350
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E)-farnesyl diphosphate + 5 isopentenyl diphosphate = 5 diphosphate + all-trans-octaprenyl diphosphate.","definition_xrefs":["PMID:3519603","RHEA:27798","PMID:8037730"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenyl diphosphate synthase activity","termid":"GO:0120531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016765"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016765"],"is_obsolete":false,"name":"all-trans-octaprenyl-diphosphate synthase activity","secondary_identifiers":["EC:2.5.1.90"],"synonyms":[{"name":"octaprenyl pyrophosphate synthase activity","type":"exact"},{"name":"terpenyl pyrophosphate synthetase activity","type":"broad"},{"name":"trans-heptaprenyltranstransferase activity","type":"exact"},{"name":"trans-prenyltransferase activity","type":"broad"}],"termid":"GO:0106350"}


id: FYPO:0000276
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the mitotic spindle forms with microtubules emanating from only one pole.","definition_xrefs":["PomBase:mah","PMID:9763447","PMID:11792803"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic spindle","termid":"FYPO:0000338"},{"relation_name":"output_of","term_name":"abolished mitotic spindle midzone assembly","termid":"FYPO:0005344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000120"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000641","FYPO:0000337","FYPO:0000120","FYPO:0002399","FYPO:0000054"],"is_obsolete":false,"name":"monopolar mitotic spindle","synonyms":[{"name":"V-shaped mitotic spindle","type":"related"},{"name":"fan-shaped mitotic spindle","type":"exact"},{"name":"monopolar mitotic spindle during vegetative growth","type":"exact"},{"name":"monopolar spindle during mitosis","type":"exact"},{"name":"monopolar spindle during mitotic cell cycle","type":"exact"},{"name":"spindle defects, monopolar mitotic spindle","type":"exact"},{"name":"spindle defects, monopolar spindle","type":"exact"}],"termid":"FYPO:0000276"}


id: GO:0036195
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the plasma membrane surrounding a muscle cell projection.","definition_xrefs":["PMID:15930100","GOC:kmv","CL:0000187","PMID:22464329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell projection membrane","termid":"GO:0031253"},{"relation_name":"part_of","term_name":"muscle cell projection","termid":"GO:0036194"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"muscle cell projection membrane","termid":"GO:0036195"}


id: PBO:0069707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 987, pseudogene","termid":"PBO:0069707"}


id: PBO:0086598
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 is cell-cycle regulated as shown by microarray analysis; potential regulatory target of Mbp1p, which binds to the YJL181W promoter region; contains a PH-like domain; RBH1 has a paralog, RBH2, that arose from the whole genome duplication","termid":"PBO:0086598"}


id: PBO:0042888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 410","termid":"PBO:0042888"}


id: PBO:0058984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MLLT3 super elongation complex subunit","termid":"PBO:0058984"}


id: FYPO:0009104
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the recoil time of the cytokynetic ring after ring ablation is increased with respect to wild type. Experimentally, a localised cut or ablation is typically achieved using a laser. The recoil time is the time it takes the recoil to stop after laser ablation. This timing, in combination with the recoil distance are used to compute effective stiffness and drag of the ring components. See PMID:36980258.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring","termid":"FYPO:0004736"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0004803","FYPO:0000631"],"is_obsolete":false,"name":"increased actomyosin contractile ring recoil time after ring ablation","secondary_identifiers":["PMID:36980258"],"synonyms":[{"name":"increased cytokinetic ring recoil distance after laser ablation","type":"broad"}],"termid":"FYPO:0009104"}


id: PBO:0071065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 67","termid":"PBO:0071065"}


id: GO:0097331
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cytarabine stimulus.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to glycoside","termid":"GO:1903416"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cytarabine","termid":"GO:0097331"}


id: GO:0075300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of zygospore formation, a process in which a thick-walled spore of some algae and fungi is formed by union of two similar sexual cells, usually serves as a resting spore, and produces the sporophytic phase.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of sexual sporulation resulting in formation of a cellular spore","termid":"GO:0043942"},{"relation_name":"is_a","term_name":"regulation of zygospore formation","termid":"GO:0075298"},{"relation_name":"negatively_regulates","term_name":"zygospore formation","termid":"GO:0034296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of zygospore formation","termid":"GO:0075300"}


id: GO:0023058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulation of a signal transduction pathway in response to a stimulus upon prolonged exposure to that stimulus.","definition_xrefs":["GOC:mtg_signal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"adaptation of signaling pathway","synonyms":[{"name":"adaptation of signalling pathway","type":"exact"}],"termid":"GO:0023058"}


id: PBO:0047049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 110 member D","termid":"PBO:0047049"}


id: MONDO:0700192
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hepatoma that occurs in a chicken.","definition_xrefs":["NCIT:C134558"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chicken neoplasm","termid":"MONDO:0700189"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chicken hepatoma","termid":"MONDO:0700192","xrefs":{"Monarch":{"xref_id":"0700192"}}}


id: PBO:0074112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 29 member 4","termid":"PBO:0074112"}


id: PBO:0071670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L37 pseudogene 2","termid":"PBO:0071670"}


id: PBO:0002344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enhancer of rudimentary homolog","termid":"PBO:0002344"}


id: PBO:0057124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 208a","termid":"PBO:0057124"}


id: PBO:0003871
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.6.3.4","termid":"PBO:0003871"}


id: GO:0019780
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the activation of the small ubiquitin-related modifier FAT10, through the formation of an ATP-dependent high-energy thiolester bond.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like modifier activating enzyme activity","termid":"GO:0008641"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"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:0140096","GO:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"FAT10 activating enzyme activity","termid":"GO:0019780"}


id: MONDO:0014058
data:
  {"annotated_genes":["SJAG_02908"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85451],"is_not":false,"summary":null,"term":"MONDO:0014058"}]},"cv_name":"mondo","definition":"A rare genetic disease characterized by facial dysmorphism with malar hypoplasia and high forehead, immunodeficiency resulting in recurrent infections, impaired growth (with normal growth hormone production and response) resulting in short stature, and livedo affecting face and extremities. Immunological analyzes show low memory B-cell and naïve T cell counts, decreased T cell proliferation, and reduced IgM, IgG2 and IgG4 titers. Patients do not exhibit increased susceptibility to cancer.","definition_xrefs":["Orphanet:352712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02908":null},"genotype_count":0,"is_obsolete":false,"name":"facial dysmorphism-immunodeficiency-livedo-short stature syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:615139","UMLS:C3554576","GARD:17528","MEDGEN:767490"],"synonyms":[{"name":"facial dysmorphism, immunodeficiency, livedo, and short stature","type":"related"},{"name":"fils","type":"related"},{"name":"fils syndrome","type":"exact"}],"termid":"MONDO:0014058","terms_by_termid":{"MONDO:0014058":null},"xrefs":{"Monarch":{"xref_id":"0014058"}}}


id: MONDO:0002469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma arising in a pre-existing pleomorphic adenoma in the lacrimal gland.","definition_xrefs":["NCIT:C6804"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal gland carcinoma","termid":"MONDO:0002463"},{"relation_name":"is_a","term_name":"carcinoma ex pleomorphic adenoma","termid":"MONDO:0002472"}],"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:0005328","MONDO:0004992"],"is_obsolete":false,"name":"lacrimal gland carcinoma ex pleomorphic adenoma","secondary_identifiers":["DOID:296","MEDGEN:138058","MONDO:0021278","SCTID:254989000","UMLS:C0346342"],"synonyms":[{"name":"carcinoma Ex pleomorphic adenoma of the lacrimal gland","type":"exact"},{"name":"carcinoma ex pleomorphic adenoma of lacrimal gland","type":"exact"},{"name":"carcinoma ex pleomorphic adenoma of the lacrimal gland","type":"exact"},{"name":"lacrimal gland carcinoma ex pleomorphic adenoma","type":"exact"},{"name":"lacrimal gland malignant mixed neoplasm","type":"exact"},{"name":"lacrimal gland malignant mixed tumor","type":"exact"},{"name":"lacrimal gland malignant mixed tumour","type":"exact"},{"name":"malignant mixed neoplasm of lacrimal gland","type":"exact"},{"name":"malignant mixed neoplasm of the lacrimal gland","type":"exact"},{"name":"malignant mixed tumor of lacrimal gland","type":"exact"},{"name":"malignant mixed tumor of the lacrimal gland","type":"exact"},{"name":"malignant mixed tumour of lacrimal gland","type":"exact"},{"name":"malignant mixed tumour of the lacrimal gland","type":"exact"},{"name":"mixed lacrimal gland cancer","type":"related"}],"termid":"MONDO:0002469","xrefs":{"Monarch":{"xref_id":"0002469"}}}


id: PBO:0082173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP/ATP transporter; member of the Ca2+-binding subfamily of mitochondrial carriers, with two EF-hand motifs; transport activity of either Sal1p or Pet9p is critical for viability; polymorphic in different S. cerevisiae strains","termid":"PBO:0082173"}


id: GO:0090165
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The asymmetric formation of a continuous ribbon of interconnected Golgi stacks of flat cisternae that modulates the controlled release of a substance from a polarized epithelial cell.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of secretion","termid":"GO:0051046"},{"relation_name":"is_a","term_name":"asymmetric Golgi ribbon formation","termid":"GO:0090164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007163"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0007163","GO:0006810"],"is_obsolete":false,"name":"regulation of secretion by asymmetric Golgi ribbon formation","termid":"GO:0090165"}


id: PBO:0044233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cullin 2","termid":"PBO:0044233"}


id: PBO:0052384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 25","termid":"PBO:0052384"}


id: PBO:0049178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GREB1 like retinoic acid receptor coactivator","termid":"PBO:0049178"}


id: PBO:0066379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIG-I dependent antiviral response regulator RNA","termid":"PBO:0066379"}


id: GO:0002272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an immature plasmacytoid dendritic cell acquires the specialized features of a mature plasmacytoid dendritic cell contributing to an immune response.","definition_xrefs":["GOC:add","PMID:15990333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasmacytoid dendritic cell activation involved in immune response","termid":"GO:0002271"},{"relation_name":"is_a","term_name":"plasmacytoid dendritic cell differentiation","termid":"GO:0002273"}],"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":"plasmacytoid dendritic cell differentiation involved in immune response","synonyms":[{"name":"plasmacytoid dendritic cell differentiation during immune response","type":"related"}],"termid":"GO:0002272"}


id: PBO:0070817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 47","termid":"PBO:0070817"}


id: GO:0052010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the breakdown of cellulose in the host cell wall. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete catabolism by symbiont of host cell wall cellulose (obsolete GO:0052010)","synonyms":[{"name":"catabolism by organism of host cell wall cellulose","type":"exact"}],"termid":"GO:0052010"}


id: GO:0021638
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the trigeminal nerve. This process pertains to the initial formation of a structure from unspecified parts. The trigeminal nerve is composed of three large branches. They are the ophthalmic (V1, sensory), maxillary (V2, sensory) and mandibular (V3, motor and sensory) branches. The sensory ophthalmic branch travels through the superior orbital fissure and passes through the orbit to reach the skin of the forehead and top of the head. The maxillary nerve contains sensory branches that reach the pterygopalatine fossa via the inferior orbital fissure (face, cheek and upper teeth) and pterygopalatine canal (soft and hard palate, nasal cavity and pharynx). The motor part of the mandibular branch is distributed to the muscles of mastication, the mylohyoid muscle and the anterior belly of the digastric. The mandibular nerve also innervates the tensor veli palatini and tensor tympani muscles. The sensory part of the mandibular nerve is composed of branches that carry general sensory information from the mucous membranes of the mouth and cheek, anterior two-thirds of the tongue, lower teeth, skin of the lower jaw, side of the head and scalp and meninges of the anterior and middle cranial fossae.","definition_xrefs":["ISBN:0838580343","GOC:cls","GOC:jid","GO_REF:0000021","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve formation","termid":"GO:0021603"},{"relation_name":"part_of","term_name":"trigeminal nerve morphogenesis","termid":"GO:0021636"}],"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":"trigeminal nerve formation","synonyms":[{"name":"CN V biosynthesis","type":"related"},{"name":"CN V formation","type":"related"}],"termid":"GO:0021638"}


id: PBO:0076022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine kinase 17b","termid":"PBO:0076022"}


id: GO:1902112
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a diethyl maleate stimulus.","definition_xrefs":["GOC:TermGenie","PMID:12100563"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to diethyl maleate","termid":"GO:1902111"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to diethyl maleate","termid":"GO:1902112"}


id: PBO:0035772
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K14_acetylation_at_centromere_outer_repeat_during_vegetative_growth","termid":"PBO:0035772"}


id: MONDO:1012572
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cancer that occurs in pigs.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer, non-human animal","termid":"MONDO:1011828"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer, pig","secondary_identifiers":["OMIA:002587-9823"],"termid":"MONDO:1012572","xrefs":{"Monarch":{"xref_id":"1012572"}}}


id: PBO:0080032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 17 like family member 18","termid":"PBO:0080032"}


id: GO:0002337
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which B cells acquire the specialized features of B-1a B cells. B-1a B cells are B-1 cells that express CD5 and arise from fetal liver precursors.","definition_xrefs":["ISBN:0781735149","GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B-1 B cell differentiation","termid":"GO:0001923"}],"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":"B-1a B cell differentiation","synonyms":[{"name":"B-1a B cell development","type":"related"},{"name":"B-1a B lymphocyte differentiation","type":"exact"},{"name":"B-1a B-cell differentiation","type":"exact"},{"name":"B-1a B-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002337"}


id: PBO:0042652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDYL pseudogene 1","termid":"PBO:0042652"}


id: PBO:0027390
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_glutathione_disulfide_oxidoreductase_activity","termid":"PBO:0027390"}


id: PR:Q8WZK3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ibp1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q8WZK3"],"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":"dual specificity phosphatase ibp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC839.07","synonyms":[{"name":"Itsy bitsy phosphatase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ibp1","type":"exact"},{"name":"cdc25-like phosphatase ibp1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q8WZK3"}


id: PBO:0089131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"helper of TIM Hot15","termid":"PBO:0089131"}


id: PBO:0047023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A26","termid":"PBO:0047023"}


id: GO:0006399
data:
  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id: PBO:0046550
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id: MONDO:0011099
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Human HOXA1 syndromes is characterized by deafness, central hypoventilation, congenital ocular paralysis and developmental retardation. Cardiac anomalies and paralysis of the vocal chords may also be present. Six cases have been reported so far. Transmission is thought to be autosomal recessive.","definition_xrefs":["Orphanet:69739"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"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"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"human HOXA1 syndromes","secondary_identifiers":["UMLS:C1832215","GARD:8333","DOID:0050682","SCTID:720518006","MEDGEN:330410","OMIM:601536"],"synonyms":[{"name":"ABDS","type":"related"},{"name":"ABSD","type":"exact"},{"name":"Athabascan brainstem dysgenesis syndrome","type":"exact"},{"name":"Athabaskan brainstem dysgenesis","type":"related"},{"name":"Athabaskan brainstem dysgenesis syndrome","type":"exact"},{"name":"BSAS","type":"related"},{"name":"Bosley Salih Alorainy syndrome","type":"related"},{"name":"Bosley-Salih-Alorainy syndrome","type":"related"},{"name":"Human HOXA1 syndromes","type":"related"},{"name":"Navajo brainstem syndrome","type":"exact"}],"termid":"MONDO:0011099","xrefs":{"Monarch":{"xref_id":"0011099"}}}


id: PBO:0065956
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD21 pseudogene 1","termid":"PBO:0065956"}


id: FYPO:0003370
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id: PATO:0001492
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id: PBO:0040044
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin related protein 2/3 complex subunit 1A","termid":"PBO:0040044"}


id: PR:O94697
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A replication factor C subunit 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"replication factor C subunit 5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC83.14c","secondary_identifiers":["UniProtKB:O94697"],"synonyms":[{"name":"Spom972h-RFC3","type":"exact"},{"name":"replication factor C5 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94697"}


id: GO:0047796
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cyclohexane-1,3-dione + H2O = 5-oxohexanoate + H+.","definition_xrefs":["RHEA:16473","EC:3.7.1.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances","termid":"GO:0016823"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"cyclohexane-1,3-dione hydrolase activity","secondary_identifiers":["KEGG_REACTION:R03211","MetaCyc:CYCLOHEXANE-13-DIONE-HYDROLASE-RXN"],"synonyms":[{"name":"1,3-cyclohexanedione hydrolase activity","type":"related"},{"name":"cyclohexane-1,3-dione acylhydrolase (decyclizing)","type":"related"}],"termid":"GO:0047796"}


id: PBO:0091718
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane palmitoyltransferase Pfa5","termid":"PBO:0091718"}


id: GO:0055069
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involved in the maintenance of an internal steady state of zinc ions within an organism or cell.","definition_xrefs":["GOC:ai","GOC:jid","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete zinc ion homeostasis (obsolete GO:0055069)","synonyms":[{"name":"zinc homeostasis","type":"broad"}],"termid":"GO:0055069"}


id: GO:1904608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. 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 monosodium L-glutamate stimulus.","definition_xrefs":["PMID:21389115","GO_REF:0000071","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete response to monosodium L-glutamate (obsolete GO:1904608)","termid":"GO:1904608"}


id: GO:0021740
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the pontine nucleus over time, from its formation to the mature structure.","definition_xrefs":["GOC:dgh","GOC:cls","GOC:dph","GOC:curators","GO_REF:0000021","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trigeminal sensory nucleus development","termid":"GO:0021730"}],"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":"principal sensory nucleus of trigeminal nerve development","synonyms":[{"name":"pontine nucleus development","type":"broad"}],"termid":"GO:0021740"}


id: PBO:0070536
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 2","termid":"PBO:0070536"}


id: PBO:0072548
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulatory associated protein of MTOR complex 1","termid":"PBO:0072548"}


id: FYPO:0006010
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a mating projection is assembled but does not meet a cell of the opposite mating type.","definition_xrefs":["PomBase:mah","PMID:28410370"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating","termid":"FYPO:0000031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000301"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000301","FYPO:0001985"],"is_obsolete":false,"name":"abolished shmoo contact with partner cell","synonyms":[{"name":"abolished shmoo contact with partner cell during conjugation","type":"exact"},{"name":"shmoo does not meet partner cell","type":"exact"},{"name":"shmoo without partner cell","type":"broad"}],"termid":"FYPO:0006010"}


id: PBO:0091380
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial CHCH domain protein Mix17","termid":"PBO:0091380"}


id: PBO:0040366
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase peripheral stalk-membrane subunit b pseudogene 3","termid":"PBO:0040366"}


id: GO:0110063
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the angiotensin-activated signaling pathway.","definition_xrefs":["GOC:lf","PMID:28784619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of G protein-coupled receptor signaling pathway","termid":"GO:0045745"},{"relation_name":"is_a","term_name":"regulation of angiotensin-activated signaling pathway","termid":"GO:0110061"},{"relation_name":"positively_regulates","term_name":"angiotensin-activated signaling pathway","termid":"GO:0038166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of angiotensin-activated signaling pathway","termid":"GO:0110063"}


id: PBO:0043530
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cordon-bleu WH2 repeat protein like 1","termid":"PBO:0043530"}


id: FYPO:0003656
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to vanadate ions (VO4(3-)). Cells stop growing (and may die) at a concentration of vanadate ions that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0000003","FYPO:0005447","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to vanadate","secondary_identifiers":["FYPO:0000718"],"synonyms":[{"name":"hypersensitive to trisodium vanadate","type":"narrow"},{"name":"hypersensitive to vanadate","type":"exact"},{"name":"sensitive to sodium orthovanadate","type":"narrow"},{"name":"sensitive to trisodium vanadate","type":"narrow"},{"name":"sensitive to trisodium vanadate during mitotic cell cycle","type":"related"},{"name":"sensitive to trisodium vanadate during vegetative growth","type":"narrow"},{"name":"sensitive to vanadate during mitotic cell cycle","type":"related"},{"name":"sensitive to vanadate during vegetative growth","type":"exact"},{"name":"sensitive to vanadate ions","type":"exact"},{"name":"sensitive to vanadate(3-)","type":"exact"},{"name":"sensitive to vanadium oxoanion","type":"broad"}],"termid":"FYPO:0003656"}


id: MONDO:1011778
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic active hepatitis, non-human animal","secondary_identifiers":["OMIA:001093"],"termid":"MONDO:1011778","xrefs":{"Monarch":{"xref_id":"1011778"}}}


id: PBO:0060481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nanog homeobox pseudogene 3","termid":"PBO:0060481"}


id: FYPO:0006903
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 total amount of protein measured in a cell is lower than normal during S phase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah","PomBase:jh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased total protein level during vegetative growth","termid":"FYPO:0006846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0006551","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased total protein level during mitotic S phase","synonyms":[{"name":"decreased total protein accumulation during mitotic S phase","type":"related"},{"name":"decreased total protein content during mitotic S phase","type":"exact"},{"name":"decreased total protein level during S phase of mitotic cell cycle","type":"exact"},{"name":"reduced total protein level during mitotic S phase","type":"exact"}],"termid":"FYPO:0006903"}


id: PBO:0109515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VCP nuclear cofactor family member 2","termid":"PBO:0109515"}


id: GO:0030733
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + a fatty acid = S-adenosyl-L-homocysteine + a fatty acid methyl ester.","definition_xrefs":["EC:2.1.1.15"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"fatty acid O-methyltransferase activity","secondary_identifiers":["MetaCyc:FATTY-ACID-O-METHYLTRANSFERASE-RXN","RHEA:23012"],"synonyms":[{"name":"S-adenosyl-L-methionine:fatty-acid O-methyltransferase activity","type":"related"},{"name":"fatty acid methyltransferase activity","type":"related"},{"name":"fatty-acid O-methyltransferase activity","type":"exact"}],"termid":"GO:0030733"}


id: PBO:0057677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1268a","termid":"PBO:0057677"}


id: PBO:0069487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 754, pseudogene","termid":"PBO:0069487"}


id: PBO:0004263
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.3.3.2","termid":"PBO:0004263"}


id: PBO:0053207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galectin 7","termid":"PBO:0053207"}


id: PBO:0074302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLX1 homolog B, structure-specific endonuclease subunit","termid":"PBO:0074302"}


id: MONDO:0000567
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete C1 inhibitor deficiency (obsolete MONDO:0000567)","termid":"MONDO:0000567","xrefs":{"Monarch":{"xref_id":"0000567"}}}


id: FYPO:0004729
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 cytoplasmic microtubules are formed by the extension of existing nuclear microtubules arising from fragmentation of the mitotic spindle. Normally, cytoplasmic microtubules are nucleated from microtubule organizing centers in the cytoplasm.","definition_xrefs":["PMID:15772152","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic microtubule formation from nuclear microtubules","termid":"FYPO:0004727"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"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:0000054","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"cytoplasmic microtubule formation from nuclear microtubules following spindle microtubule fragmentation","synonyms":[{"name":"cytoplasmic microtubule formation from nuclear microtubules following mitotic spindle microtubule fragmentation","type":"exact"},{"name":"cytoplasmic microtubule formation from nuclear microtubules following spindle microtubule fragmentation during mitotic cell cycle","type":"related"},{"name":"cytoplasmic microtubule formation from nuclear microtubules following spindle microtubule fragmentation during vegetative growth","type":"exact"}],"termid":"FYPO:0004729"}


id: PBO:0113258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Permease of basic amino acids in vacuolar membrane; targeted to vacuole via AP-3 pathway","termid":"PBO:0113258"}


id: PBO:0109140
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 3110","termid":"PBO:0109140"}


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


id: PBO:0002648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mo25 family protein Pmo25","termid":"PBO:0002648"}


id: GO:0044717
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 8-hydroxy-dADP + H2O = 8-hydroxy-dAMP + phosphate.","definition_xrefs":["PMID:22556419","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside diphosphate phosphatase activity","termid":"GO:0017110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"8-hydroxy-dADP phosphatase activity","secondary_identifiers":["Reactome:R-HSA-2395965"],"termid":"GO:0044717"}


id: MOD:00759
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod N-linked glycosylation","definition_xrefs":["Unimod:307"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N4-glycosyl-L-asparagine","termid":"MOD:00160"},{"relation_name":"is_a","term_name":"complex glycosylation","termid":"MOD:00725"}],"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":"fucosylated biantennary (-1 galactose) N4-glycosylated asparagine","synonyms":[{"name":"Fucosylated biantennary (-1 galactose)","type":"related"},{"name":"dHex(1)Hex(4)HexNAc(4)","type":"related"}],"termid":"MOD:00759"}


id: GO:0046011
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of oskar mRNA translation. To ensure the localization of Oskar protein at the posterior pole of the oocyte, translation of oskar mRNA is repressed during its transport to the posterior pole and activated upon localization of the mRNA at the posterior cortex.","definition_xrefs":["PMID:12538512","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation","termid":"GO:0006417"}],"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 oskar mRNA translation","termid":"GO:0046011"}


id: FYECO:0000461
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"cells are first grown in medium containing latrunculin A, this medium is then replaced with medium containing no latrunculin A .","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping growth medium","termid":"FYECO:0000009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recovery after latrunculin A treatment","termid":"FYECO:0000461"}


id: PBO:0069113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 362, pseudogene","termid":"PBO:0069113"}


id: PBO:0004817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L19","termid":"PBO:0004817"}


id: MONDO:0003495
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell tumor that arises from the ovary and is not associated with a germ cell tumor.","definition_xrefs":["NCIT:C40092"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian epithelial tumor","termid":"MONDO:0002229"},{"relation_name":"is_a","term_name":"squamous cell neoplasm","termid":"MONDO:0002532"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian squamous cell neoplasm","secondary_identifiers":["DOID:5532"],"synonyms":[{"name":"ovarian squamous cell neoplasm","type":"exact"},{"name":"ovarian squamous cell tumor","type":"exact"},{"name":"ovarian squamous cell tumour","type":"exact"},{"name":"ovary squamous cell neoplasm","type":"exact"}],"termid":"MONDO:0003495","xrefs":{"Monarch":{"xref_id":"0003495"}}}


id: PBO:0000396
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.2","termid":"PBO:0000396"}


id: PBO:0116757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMARCE1 pseudogene 3","termid":"PBO:0116757"}


id: MONDO:1012831
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any progressive retinal atrophy that occurs in the Miniature Schnauzer breed of dog and is characterized by an average age of onset of seven years, mild clinical signs, and slow progression.","definition_xrefs":["PMID:32150541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive retinal atrophy, dog","termid":"MONDO:1012226"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive retinal atrophy, Miniature Schnauzer, dog","secondary_identifiers":["OMIA:002253-9615"],"termid":"MONDO:1012831","xrefs":{"Monarch":{"xref_id":"1012831"}}}


id: MONDO:0018238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare bone disease related to a common gene or pathway defect (obsolete MONDO:0018238)","termid":"MONDO:0018238","xrefs":{"Monarch":{"xref_id":"0018238"}}}


id: PBO:0057640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1231","termid":"PBO:0057640"}


id: GO:1902716
data:
  {"annotated_genes":["SJAG_04703","SJAG_04509","SJAG_03486","SJAG_02320","SJAG_02166","SJAG_02222","SJAG_03011","SJAG_00514","SJAG_05285","SJAG_02838","SJAG_04666","SJAG_03126","SJAG_03625","SJAG_03637","SJAG_03581","SJAG_02169","SJAG_03705","SJAG_01925"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70552,88195,90175,91035,91064,92731,94892,106423,111079,112275,113372,114479,116134,116496,116804,118226,118960,119158],"is_not":false,"summary":null,"term":"GO:1902716"}]},"cv_name":"cellular_component","definition":"Any cell cortex that is part of a growing cell tip.","definition_xrefs":["GOC:TermGenie","PMID:24146635","GO_REF:0000064"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cortex of cell tip","termid":"GO:0051285"},{"relation_name":"part_of","term_name":"growing cell tip","termid":"GO:0035838"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_01925":null,"SJAG_02166":null,"SJAG_02169":null,"SJAG_02222":null,"SJAG_02320":null,"SJAG_02838":null,"SJAG_03011":null,"SJAG_03126":null,"SJAG_03486":null,"SJAG_03581":null,"SJAG_03625":null,"SJAG_03637":null,"SJAG_03705":null,"SJAG_04509":null,"SJAG_04666":null,"SJAG_04703":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005938"},{"rel_name":"part_of","termid":"GO:0005938"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005938","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cell cortex of growing cell tip","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"cell cortex of growing cell end","type":"exact"}],"termid":"GO:1902716","terms_by_termid":{"GO:1902716":null}}


id: PBO:0041035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B-Raf proto-oncogene, serine/threonine kinase","termid":"PBO:0041035"}


id: GO:0071050
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The enzymatic addition of a sequence of adenylyl residues at the 3' end of snoRNA class molecule (referred to as an sRNA in Archaea). In eukaryotes, this occurs in conjunction with termination of transcription of precursor snoRNA molecules and may occur post-transcriptionally on incorrectly processed molecules targeted for degradation.","definition_xrefs":["PMID:18951092","GOC:dgf","GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete sno(s)RNA polyadenylation (obsolete GO:0071050)","synonyms":[{"name":"sRNA polyadenylation","type":"narrow"},{"name":"snoRNA polyadenylation","type":"narrow"}],"termid":"GO:0071050"}


id: PBO:0001624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF3c","termid":"PBO:0001624"}


id: PBO:0061202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NOC2 like nucleolar associated transcriptional repressor pseudogene 2","termid":"PBO:0061202"}


id: PBO:0041723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium/calmodulin dependent protein kinase ID","termid":"PBO:0041723"}


id: PATO:0001010
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001010 relative intensity (obsolete PATO:0001010)","termid":"PATO:0001010"}


id: MONDO:0800140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any non-severe combined immunodeficiency in which the cause of the disease is variation in the ITPKB gene.","definition_xrefs":["PMID:31987846"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"}],"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":"ITPKB deficiency","termid":"MONDO:0800140","xrefs":{"Monarch":{"xref_id":"0800140"}}}


id: GO:0071379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a prostagladin stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to hormone stimulus","termid":"GO:0032870"},{"relation_name":"is_a","term_name":"response to prostaglandin","termid":"GO:0034694"},{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to prostaglandin stimulus","termid":"GO:0071379"}


id: PBO:0018084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein Tam13","termid":"PBO:0018084"}


id: FYPO:0004829
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a phosphatase activity is decreased during a cellular response to adenine starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased phosphatase activity","termid":"FYPO:0004304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000707","FYPO:0001985","FYPO:0000661","FYPO:0000652"],"is_obsolete":false,"name":"decreased phosphatase activity during cellular response to adenine starvation","synonyms":[{"name":"decreased phosphatase activity during adenine starvation","type":"exact"},{"name":"reduced phosphatase activity during cellular response to adenine starvation","type":"exact"}],"termid":"FYPO:0004829"}


id: PATO:0002317
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A convex quadrilateral is a parallelogram if and only if any one of the following statements are true:\\n1. Each diagonal divides the quadrilateral into two congruent triangles with the same orientation.\\n2. The opposite sides are congruent in pairs.\\n3. The diagonals bisect each other.\\n4. The opposite angles are congruent in pairs.\\n5. The sum of the squares of the sides equals the sum of the squares of the diagonals. (This is the parallelogram law)\\n6.It possesses rotational symmetry.\\n7.One pair of opposite sides are parallel and congruent.\\n8.Two pairs of adjacent angles are supplementary.","definition_xrefs":["wikipedia:Parallelogram"],"direct_ancestors":[{"relation_name":"is_a","term_name":"quadrangular","termid":"PATO:0001988"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parallelogram","termid":"PATO:0002317"}


id: PBO:0002884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HECT-type ubiquitin ligase E3 Ptr1","termid":"PBO:0002884"}


id: MONDO:0017794
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Xq12-q13.3 duplication syndrome is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the long arm of chromosome X, characterized by global developmental delay, autistic behavior, microcephaly and facial dysmorphism (including down-slanting palpebral fissures, depressed nasal bridge, anteverted nares, long philtrum, down-slanting corners of the mouth). Seizures have also been reported in some patients.","definition_xrefs":["Orphanet:314389"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome X","termid":"MONDO:0017010"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xq12-q13.3 duplication syndrome","secondary_identifiers":["SCTID:764711007","GARD:21369","UMLS:C4707094","MEDGEN:1648034"],"synonyms":[{"name":"dup(X)(q12-q13.3)","type":"exact"}],"termid":"MONDO:0017794","xrefs":{"Monarch":{"xref_id":"0017794"}}}


id: PBO:0069870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1157, pseudogene","termid":"PBO:0069870"}


id: MONDO:0021440
data:
  {"annotated_genes":["SJAG_02855","SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"},{"annotations":[87117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044792"},{"annotations":[86209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008097"},{"annotations":[85790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009578"},{"annotations":[85367],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008093"}]},"cv_name":"mondo","definition":"A benign neoplasm that involves the zone of skin.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system benign neoplasm","termid":"MONDO:0000652"},{"relation_name":"is_a","term_name":"skin neoplasm","termid":"MONDO:0002531"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02855":null,"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"benign neoplasm of skin","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:92384009","ICD9:216.9","NCIT:C2896","UMLS:C0004998","ICD9:216.8","MEDGEN:2197"],"synonyms":[{"name":"benign cutaneous neoplasm","type":"exact"},{"name":"benign cutaneous tumor","type":"exact"},{"name":"benign cutaneous tumour","type":"exact"},{"name":"benign neoplasm of the skin","type":"exact"},{"name":"benign skin neoplasm","type":"exact"},{"name":"benign skin tumor","type":"exact"},{"name":"benign skin tumour","type":"exact"},{"name":"benign tumor of skin","type":"exact"},{"name":"benign tumor of the skin","type":"exact"},{"name":"benign tumour of skin","type":"exact"},{"name":"benign tumour of the skin","type":"exact"},{"name":"skin neoplasms, benign","type":"exact"},{"name":"zone of skin benign neoplasm","type":"exact"}],"termid":"MONDO:0021440","terms_by_termid":{"MONDO:0008093":null,"MONDO:0008097":null,"MONDO:0009578":null,"MONDO:0010621":null,"MONDO:0044792":null},"xrefs":{"Monarch":{"xref_id":"0021440"}}}


id: PBO:0049567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B histone pseudogene 3","termid":"PBO:0049567"}


id: GO:0062034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-pipecolic acid, a metabolite of lysine.","definition_xrefs":["PMID:27758894","PMID:28330936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"L-pipecolic acid biosynthetic process","synonyms":[{"name":"L-pipecolate biosynthetic process","type":"exact"}],"termid":"GO:0062034"}


id: GO:0090078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a smooth muscle cell acquires the specialized features of a foam cell. A foam cell is a type of cell containing lipids in small vacuoles and typically seen in atherosclerotic lesions, as well as other conditions.","definition_xrefs":["GOC:BHF","GOC:tb","GOC:add","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"foam cell differentiation","termid":"GO:0090077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"smooth muscle derived foam cell differentiation","termid":"GO:0090078"}


id: PBO:0063737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 2","termid":"PBO:0063737"}


id: PBO:0010008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation RNA helicase Sum3","termid":"PBO:0010008"}


id: PBO:0067814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 116","termid":"PBO:0067814"}


id: MONDO:0006145
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A slow-growing malignant bone tumor arising from the remnants of the notochord and occurring in the base of the skull. The tumor is characterized by a lobulated growth pattern, myxoid stroma formation, and the presence of physaliphorous cells and cartilage.","definition_xrefs":["NCIT:C6902"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chordoma","termid":"MONDO:0008978"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroid chordoma","secondary_identifiers":["MEDGEN:224768","UMLS:C1266173","EFO:1000174","ICDO:9371/3","DOID:4152"],"synonyms":[{"name":"chondroid chordoma","type":"exact"},{"name":"chondroid chordoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0006145","xrefs":{"Monarch":{"xref_id":"0006145"}}}


id: PBO:0060441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NACA pseudogene 10","termid":"PBO:0060441"}


id: PBO:0074254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier organic anion transporter family member 1B7 (putative)","termid":"PBO:0074254"}


id: MONDO:0011236
data:
  {"annotated_genes":["SJAG_04334","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86817,86818],"is_not":false,"summary":null,"term":"MONDO:0011236"}]},"cv_name":"mondo","definition":"Hyperinsulism due to glucokinase deficiency (HIGCK) is a form of diazoxide-sensitive diffuse hyperinsulinism, caused by a lowered threshold for insulin release, characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia) and recurrent episodes of profound hypoglycemia induced by fasting and protein rich meals, requiring rapid and intensive treatment to prevent neurological sequelae.","definition_xrefs":["Orphanet:79299"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diazoxide-sensitive diffuse hyperinsulinism","termid":"MONDO:0015624"},{"relation_name":"is_a","term_name":"disorder of glycolysis","termid":"MONDO:0017688"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0019254","MONDO:0037792","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"hyperinsulinism due to glucokinase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:717182006","UMLS:C1865290","MEDGEN:355435","GARD:2818","DOID:0070216","OMIM:602485","MESH:C538374"],"synonyms":[{"name":"HHF3","type":"related"},{"name":"hyperinsulinemic hypoglycemia due to glucokinase deficiency","type":"exact"},{"name":"hyperinsulinemic hypoglycemia familial 3","type":"related"},{"name":"hyperinsulinemic hypoglycemia, familial, 3","type":"related"},{"name":"hyperinsulinemic hypoglycemia, familial, type 3","type":"exact"}],"termid":"MONDO:0011236","terms_by_termid":{"MONDO:0011236":null},"xrefs":{"Monarch":{"xref_id":"0011236"}}}


id: PBO:0060329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin IG","termid":"PBO:0060329"}


id: PBO:0080081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 43","termid":"PBO:0080081"}


id: GO:0015375
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: glycine(out) + Na+(out) = glycine(in) + Na+(in).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neutral L-amino acid:sodium symporter activity","termid":"GO:0005295"},{"relation_name":"is_a","term_name":"organic acid:sodium symporter activity","termid":"GO:0005343"},{"relation_name":"is_a","term_name":"glycine transmembrane transporter activity","termid":"GO:0015187"}],"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:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"glycine:sodium symporter activity","secondary_identifiers":["Reactome:R-HSA-444120","Reactome:R-HSA-5660840","RHEA:68228","GO:0015656"],"termid":"GO:0015375"}


id: GO:0140312
data:
  {"annotated_genes":["SJAG_00152","SJAG_00104","SJAG_02805","SJAG_01167","SJAG_00800","SJAG_02453","SJAG_04565","SJAG_03726","SJAG_01748","SJAG_03146","SJAG_00108","SJAG_01809","SJAG_04931","SJAG_04609","SJAG_00379"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106357,111018],"is_not":false,"summary":null,"term":"GO:0140312"},{"annotations":[58320,78073,62224,78092,111830,113119,78430,94513,96455,74683,89231,72381,108660],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035615"}]},"cv_name":"molecular_function","definition":"Binding directly to the structural scaffolding elements of a vesicle coat (such as clathrin or COPII), and bridging the membrane, cargo receptor, and membrane deformation machinery.","definition_xrefs":["PMID:25795254"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-macromolecule adaptor activity","termid":"GO:0030674"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00108":null,"SJAG_00152":null,"SJAG_00379":null,"SJAG_00800":null,"SJAG_01167":null,"SJAG_01748":null,"SJAG_01809":null,"SJAG_02453":null,"SJAG_02805":null,"SJAG_03146":null,"SJAG_03726":null,"SJAG_04565":null,"SJAG_04609":null,"SJAG_04931":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0060090","GO:0030674","GO:0003674"],"is_obsolete":false,"name":"cargo adaptor activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0098748","Reactome:R-HSA-203565","Reactome:R-HSA-203662"],"synonyms":[{"name":"endocytic adaptor activity","type":"narrow"}],"termid":"GO:0140312","terms_by_termid":{"GO:0035615":null,"GO:0140312":null}}


id: MOD:00942
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes four (1)H protium atoms with four (2)H deuterium atoms to produce (4,4,5,5-(2)H4)-L-lysine.","definition_xrefs":["OMSSA:180","Unimod:481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deuterium tetrasubstituted residue","termid":"MOD:00837"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(4,4,5,5-(2)H4)-L-lysine","synonyms":[{"name":"4,4,5,5-D4 Lysine","type":"related"},{"name":"4,4,5,5-tetradeuterolysine","type":"exact"},{"name":"Label:2H(4)","type":"related"},{"name":"lys-2H4","type":"exact"}],"termid":"MOD:00942"}


id: PBO:0071603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 20","termid":"PBO:0071603"}


id: GO:0050003
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,10-methylenetetrahydrofolate + dCMP = 2'-deoxy-5-methyl-5'-cytidylate + 7,8-dihydrofolate.","definition_xrefs":["EC:2.1.1.54","RHEA:11568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-methyltransferase activity","termid":"GO:0008169"}],"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:0016741"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"deoxycytidylate C-methyltransferase activity","secondary_identifiers":["MetaCyc:DEOXYCYTIDYLATE-C-METHYLTRANSFERASE-RXN","KEGG_REACTION:R01670"],"synonyms":[{"name":"5,10-methylenetetrahydrofolate:dCMP C-methyltransferase activity","type":"related"},{"name":"dCMP methyltransferase activity","type":"related"},{"name":"deoxycytidylate methyltransferase activity","type":"related"}],"termid":"GO:0050003"}


id: PBO:0082283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP4A phosphorylase; bifunctional diadenosine 5',5'''-P1,P4-tetraphosphate phosphorylase and ADP sulfurylase involved in catabolism of bis(5'-nucleosidyl) tetraphosphates; catalyzes phosphorolysis of dinucleoside oligophosphates, cleaving substrates' alpha/beta-anhydride bond and introducing Pi into the beta-position of the corresponding NDP formed; protein abundance increases under DNA replication stress; APA1 has a paralog, APA2, that arose from the whole genome duplication","termid":"PBO:0082283"}


id: FYPO:0002797
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of protein degradation is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"increased protein level","termid":"FYPO:0000836"},{"relation_name":"is_a","term_name":"abnormal protein degradation","termid":"FYPO:0002275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002274","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein degradation","synonyms":[{"name":"decreased protein breakdown","type":"exact"},{"name":"decreased protein catabolic process","type":"exact"},{"name":"decreased protein catabolism","type":"exact"},{"name":"reduced protein degradation","type":"exact"}],"termid":"FYPO:0002797"}


id: GO:0120143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of any ecdysone receptor signaling pathway.","definition_xrefs":["PMID:23072462","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of intracellular steroid hormone receptor signaling pathway","termid":"GO:0033144"},{"relation_name":"is_a","term_name":"regulation of ecdysone receptor signaling pathway","termid":"GO:0120141"},{"relation_name":"is_a","term_name":"negative regulation of cellular response to alcohol","termid":"GO:1905958"},{"relation_name":"negatively_regulates","term_name":"ecdysone receptor signaling pathway","termid":"GO:0035076"}],"gene_count":0,"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 ecdysone receptor signaling pathway","synonyms":[{"name":"negative regulation of ecdysone receptor-mediated signaling pathway","type":"exact"}],"termid":"GO:0120143"}


id: FYPO:0008057
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed  ability of an enzyme to catalyze consecutive reactions without releasing the substrate (i.e. template) is abnormal.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000707","FYPO:0001985","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"abnormal enzyme processivity","termid":"FYPO:0008057"}


id: GO:0018356
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The linkage of the chromophore phycobiliviolin to phycoerythrocyanin via S-phycobiliviolin-L-cysteine.","definition_xrefs":["RESID:AA0258"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-phycobiliviolin linkage via S-phycobiliviolin-L-cysteine (obsolete GO:0018356)","termid":"GO:0018356"}


id: PBO:0075326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suppressor of glucose, autophagy associated 1","termid":"PBO:0075326"}


id: MONDO:1010498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrial fibrillation that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrial fibrillation, non-human animal","termid":"MONDO:1010024"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrial fibrillation, dog","secondary_identifiers":["OMIA:001181-9615"],"termid":"MONDO:1010498","xrefs":{"Monarch":{"xref_id":"1010498"}}}


id: PBO:0046381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EGF domain specific O-linked N-acetylglucosamine transferase","termid":"PBO:0046381"}


id: PBO:0038998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin filament associated protein 1","termid":"PBO:0038998"}


id: MONDO:0014414
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lymphoproliferative syndrome","termid":"MONDO:0016537"},{"relation_name":"excluded_subClassOf","term_name":"autoimmune thrombocytopenia","termid":"MONDO:0019098"},{"relation_name":"excluded_subClassOf","term_name":"autoimmune hemolytic anemia","termid":"MONDO:0020108"},{"relation_name":"is_a","term_name":"autoimmune disease, multisystem, infantile-onset","termid":"MONDO:0000213"},{"relation_name":"is_a","term_name":"hematopoietic and lymphoid system neoplasm","termid":"MONDO:0002334"}],"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":"STAT3-related early-onset multisystem autoimmune disease","secondary_identifiers":["GARD:17737","MEDGEN:863232","OMIM:615952","NCIT:C157123","Orphanet:438159","UMLS:C4014795"],"synonyms":[{"name":"ADMIO","type":"related"},{"name":"ADMIO1","type":"related"},{"name":"autoimmune disease, multisystem, infantile-onset","type":"related"},{"name":"autoimmune disease, multisystem, infantile-onset, 1","type":"related"}],"termid":"MONDO:0014414","xrefs":{"Monarch":{"xref_id":"0014414"}}}


id: PBO:0003947
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.4.1.1","termid":"PBO:0003947"}


id: PBO:0063218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin 8","termid":"PBO:0063218"}


id: FYECO:0000152
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which mannose was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ mannose","termid":"FYECO:0000152"}


id: MONDO:0015948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic skin vascular disorder (obsolete MONDO:0015948)","secondary_identifiers":["Orphanet:183478"],"synonyms":[{"name":"genetic skin vascular disorder","type":"related"}],"termid":"MONDO:0015948","xrefs":{"Monarch":{"xref_id":"0015948"}}}


id: MONDO:0001313
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A acute serous otitis media caused by an allergen.","definition_xrefs":["DOID:11558","PMID:15301306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute serous otitis media","termid":"MONDO:0001312"},{"relation_name":"is_a","term_name":"allergic otitis media","termid":"MONDO:0021202"}],"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":"acute allergic serous otitis media","secondary_identifiers":["ICD9:381.04","SCTID:59275002","UMLS:C0155418","MEDGEN:509956"],"termid":"MONDO:0001313","xrefs":{"Monarch":{"xref_id":"0001313"}}}


id: GO:1900345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of methane biosynthetic process from methanethiol.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sulfur metabolic process","termid":"GO:0042762"},{"relation_name":"is_a","term_name":"regulation of cellular respiration","termid":"GO:0043457"},{"relation_name":"is_a","term_name":"regulation of alkane biosynthetic process","termid":"GO:1901577"},{"relation_name":"regulates","term_name":"methane biosynthetic process from methanethiol","termid":"GO:2001133"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0006790","GO:0008150"],"is_obsolete":false,"name":"regulation of methane biosynthetic process from methanethiol","termid":"GO:1900345"}


id: MONDO:0020317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute myeloid leukemia associated with t(9;11)(p22.3;q23.3) and MLLT3-KMT2A fusion protein expression. Morphologically it usually has monocytic features. It may present at any age but it is more commonly seen in children. Patients may present with disseminated intravascular coagulation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"acute myeloid leukemia with 11q23 abnormalities","secondary_identifiers":["NCIT:C82403","SCTID:444911000","Orphanet:98831","MEDGEN:266234","UMLS:C1292775","GARD:19587","ICDO:9897/3"],"synonyms":[{"name":"AML with 11q23 abnormalities","type":"exact"},{"name":"AML with t(9;11)(p22;q23); MLLT3-MLL","type":"exact"},{"name":"acute myeloid Leukaemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A","type":"exact"},{"name":"acute myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A","type":"exact"},{"name":"acute myeloid leukaemia with 11q23 (MLL) abnormalities","type":"exact"},{"name":"acute myeloid leukaemia with MLL abnormalities","type":"exact"},{"name":"acute myeloid leukaemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A","type":"exact"},{"name":"acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL","type":"exact"},{"name":"acute myeloid leukemia with 11q23 (MLL) abnormalities","type":"exact"},{"name":"acute myeloid leukemia with MLL abnormalities","type":"exact"},{"name":"acute myeloid leukemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A","type":"exact"},{"name":"acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL","type":"exact"}],"termid":"MONDO:0020317","xrefs":{"Monarch":{"xref_id":"0020317"}}}


id: PBO:0028822
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_microtubule_cytoskeleton_morphology_during_mating","termid":"PBO:0028822"}


id: GO:0045218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Maintaining the zonula adherens junction, the cell-cell adherens junction formed near the apex of epithelial cells.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adherens junction maintenance","termid":"GO:0034334"}],"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":"zonula adherens maintenance","termid":"GO:0045218"}


id: GO:0032095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a response to a food stimulus.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to nutrient levels","termid":"GO:0032107"},{"relation_name":"regulates","term_name":"response to food","termid":"GO:0032094"}],"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 response to food","termid":"GO:0032095"}


id: MONDO:1011477
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune hemolytic anemia that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune hemolytic anemia, non-human animal","termid":"MONDO:1011406"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune hemolytic anemia, dog","secondary_identifiers":["OMIA:000432-9615"],"termid":"MONDO:1011477","xrefs":{"Monarch":{"xref_id":"1011477"}}}


id: GO:0010019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a molecular signal is transduced between the chloroplast and nucleus, such that expression of nuclear encoding photosynthetic proteins is coupled with chloroplast biogenesis.","definition_xrefs":["PMID:8972595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signal transduction","termid":"GO:0035556"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"chloroplast-nucleus signaling pathway","synonyms":[{"name":"chloroplast-nucleus signalling pathway","type":"exact"}],"termid":"GO:0010019"}


id: PBO:0065054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRELI domain containing 3B pseudogene 8","termid":"PBO:0065054"}


id: MOD:01322
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other -","definition_xrefs":["Unimod:256#K","PubMed:15549660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"propionaldehyde +40","termid":"MOD:00579"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"propionaldehyde +40 - site K","synonyms":[{"name":"Delta:H(4)C(3)","type":"related"},{"name":"Propionaldehyde +40","type":"related"}],"termid":"MOD:01322"}


id: GO:0052857
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (R)-NADPHX = (S)-NADPHX.","definition_xrefs":["PMID:21994945"],"gene_count":0,"genotype_count":0,"name":"obsolete NADPHX epimerase activity (obsolete GO:0052857)","secondary_identifiers":["Reactome:R-HSA-6806966"],"termid":"GO:0052857"}


id: PBO:0076332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin 1","termid":"PBO:0076332"}


id: PBO:0084228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Htz1p-binding component of the SWR1 complex; exchanges histone variant H2AZ (Htz1p) for chromatin-bound histone H2A; may function as a lock that prevents removal of H2AZ from nucleosomes; required for vacuolar protein sorting","termid":"PBO:0084228"}


id: MOD:01112
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:266"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinoyl lysine","synonyms":[{"name":"nicotinyl lysyl","type":"exact"}],"termid":"MOD:01112"}


id: PBO:0014608
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear Division Arrest","termid":"PBO:0014608"}


id: MONDO:0100424
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly NRAS gene mutation. (A change in the structure of the NRAS gene.)","definition_xrefs":["NCIT:C41381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"acute myeloid leukemia, NRAS gene mutation","synonyms":[{"name":"AML, N-RAS Gene Mutation","type":"exact"},{"name":"AML, NRAS gene mutation","type":"exact"},{"name":"AML, Neuroblastoma RAS Viral Oncogene Homolog Gene Mutation","type":"exact"}],"termid":"MONDO:0100424","xrefs":{"Monarch":{"xref_id":"0100424"}}}


id: PBO:0060136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 37","termid":"PBO:0060136"}


id: PBO:0061698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear protein 2, transcriptional regulator","termid":"PBO:0061698"}


id: MONDO:0013508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopia","termid":"MONDO:0001384"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"myopia 19, autosomal dominant","secondary_identifiers":["MEDGEN:462760","OMIM:613969","UMLS:C3151410"],"synonyms":[{"name":"MYP19","type":"exact"},{"name":"myopia 19, autosomal dominant","type":"exact"}],"termid":"MONDO:0013508","xrefs":{"Monarch":{"xref_id":"0013508"}}}


id: PBO:0058344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4717","termid":"PBO:0058344"}


id: PBO:0051048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 1/OR15-1A (non-functional)","termid":"PBO:0051048"}


id: GO:0042597
data:
  {"annotated_genes":["SJAG_01970","SJAG_02093","SJAG_04067"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[103296],"is_not":false,"summary":null,"term":"GO:0042597"},{"annotations":[113663,113662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030287"}]},"cv_name":"cellular_component","definition":"The region between the inner (cytoplasmic) and outer membrane (Gram-negative Bacteria) or cytoplasmic membrane and cell wall (Fungi and Gram-positive Bacteria).","definition_xrefs":["GOC:md","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01970":null,"SJAG_02093":null,"SJAG_04067":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"periplasmic space","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0005620"],"synonyms":[{"name":"periplasm","type":"exact"}],"termid":"GO:0042597","terms_by_termid":{"GO:0030287":null,"GO:0042597":null}}


id: MONDO:0019472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Extranodal nasal NK/T cell lymphoma (NKTCL) is a rare, malignant neoplasm mainly affecting men in the fifth decade of life, that usually arises in the nose, paranasal sinuses, orbits or upper airway, and that can present with a nasal mass, nasal bleeding, nasal obstruction, palate perforation (i.e. midline perforation of the hard palate), and mid-facial and/or upper airway destructive lesions. In advanced disease stages, which are associated with a poor prognosis, NKTCL may disseminate to other organs. A few cases of NKTCL presenting primarily in the lymph nodes have also been described.","definition_xrefs":["Orphanet:86879"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma","termid":"MONDO:0005062"},{"relation_name":"is_a","term_name":"Epstein-Barr virus-associated malignant lymphoproliferative disorder","termid":"MONDO:0017343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"extranodal nasal NK/T cell lymphoma","secondary_identifiers":["ICDO:9719/3","MEDGEN:140278","GARD:7041","UMLS:C0392788","NANDO:2200027","NCIT:C4684","icd11.foundation:684005900","MedDRA:10065855","DOID:0080797"],"synonyms":[{"name":"Extranodal NK/T lymphoma-nasal","type":"exact"},{"name":"Extranodal NK/T-cell lymphoma, nasal type","type":"exact"},{"name":"NK/T-cell lymphoma","type":"exact"},{"name":"NKTCL","type":"exact"},{"name":"angiocentric T-cell lymphoma","type":"exact"},{"name":"lethal midline granuloma","type":"exact"},{"name":"nasal T/natural killer-cell lymphoma","type":"exact"},{"name":"nasal type Extranodal NK/T-cell lymphoma","type":"exact"},{"name":"reticulosis, malignant","type":"exact"}],"termid":"MONDO:0019472","xrefs":{"Monarch":{"xref_id":"0019472"}}}


id: GO:0060601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a branch forms along the side of an epithelium.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"},{"relation_name":"part_of","term_name":"morphogenesis of a branching epithelium","termid":"GO:0061138"}],"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":"lateral sprouting from an epithelium","termid":"GO:0060601"}


id: MONDO:0002623
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An osteosarcoma occurring in childhood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood malignant neoplasm","termid":"MONDO:0006517"},{"relation_name":"is_a","term_name":"osteosarcoma","termid":"MONDO:0009807"}],"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":"pediatric osteosarcoma","secondary_identifiers":["UMLS:C1332986","MEDGEN:272464","NANDO:2200048","DOID:3361","NCIT:C6585"],"synonyms":[{"name":"childhood osteogenic sarcoma","type":"exact"},{"name":"childhood osteosarcoma","type":"exact"},{"name":"childhood osteosarcoma (disease)","type":"exact"},{"name":"osteosarcoma","type":"broad"},{"name":"osteosarcoma (disease) of childhood","type":"exact"},{"name":"paediatric osteosarcoma (disease)","type":"exact"},{"name":"pediatric osteosarcoma","type":"exact"},{"name":"pediatric osteosarcoma (disease)","type":"exact"}],"termid":"MONDO:0002623","xrefs":{"Monarch":{"xref_id":"0002623"}}}


id: GO:1903505
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of establishment of actomyosin contractile ring localization involved in mitotic cell cycle.","definition_xrefs":["PMID:24165938","GOC:TermGenie","GO_REF:0000058"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of establishment of actomyosin contractile ring localization involved in mitotic cell cycle (obsolete GO:1903505)","termid":"GO:1903505"}


id: FYPO:0000448
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 MCM complex assembly is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-containing complex assembly","termid":"FYPO:0000447"}],"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:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal MCM complex assembly","synonyms":[{"name":"abnormal MCM complex assembly during mitotic cell cycle","type":"related"},{"name":"abnormal MCM complex assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0000448"}


id: MONDO:0012131
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaphyseal undermodeling, spondylar dysplasia, and overgrowth","secondary_identifiers":["MEDGEN:373306","UMLS:C1837316","GARD:10066","MESH:C537355","OMIM:608811","Orphanet:498485"],"synonyms":[{"name":"metaphyseal undermodeling, spondylar dysplasia, and overgrowth","type":"exact"},{"name":"overgrowth-metaphyseal undermodeling-spondylar dysplasia syndrome","type":"exact"}],"termid":"MONDO:0012131","xrefs":{"Monarch":{"xref_id":"0012131"}}}


id: GO:0019679
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving propionate that occur in the methylcitrate cycle.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"propionate metabolic process","termid":"GO:0019541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"propionate metabolic process, methylcitrate cycle","secondary_identifiers":["MetaCyc:PWY0-42"],"synonyms":[{"name":"propionate metabolism, methylcitrate cycle","type":"exact"}],"termid":"GO:0019679"}


id: GO:0030799
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving cyclic nucleotides.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cyclic nucleotide metabolic process (obsolete GO:0030799)","synonyms":[{"name":"regulation of cyclic nucleotide metabolism","type":"exact"}],"termid":"GO:0030799"}


id: GO:0051932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The vesicular release of gamma-aminobutyric acid (GABA). from a presynapse, across a chemical synapse, the subsequent activation of GABA receptors at the postsynapse of a target cell (neuron, muscle, or secretory cell) and the effects of this activation on the postsynaptic membrane potential and ionic composition of the postsynaptic cytosol. This process encompasses both spontaneous and evoked release of neurotransmitter and all parts of synaptic vesicle exocytosis. Evoked transmission starts with the arrival of an action potential at the presynapse.","definition_xrefs":["GOC:dos","ISBN:0126603030"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemical synaptic transmission","termid":"GO:0007268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"synaptic transmission, GABAergic","synonyms":[{"name":"GABAergic synaptic transmission","type":"exact"},{"name":"synaptic transmission, GABA mediated","type":"exact"},{"name":"synaptic transmission, gamma-aminobutyric acid mediated","type":"exact"},{"name":"synaptic transmission, gamma-aminobutyric acid-ergic","type":"exact"}],"termid":"GO:0051932"}


id: PBO:0060215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major vault protein","termid":"PBO:0060215"}


id: GO:0140619
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases a DNA strand exchange activity.","definition_xrefs":["PMID:33493431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme activator activity","termid":"GO:0008047"},{"relation_name":"positively_regulates","term_name":"DNA strand exchange activity","termid":"GO:0000150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"positively_regulates","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"positively_regulates","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"regulates","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0030234","GO:0098772","GO:0003824","GO:0140097","GO:0140677","GO:0003674"],"is_obsolete":false,"name":"DNA strand exchange activator activity","termid":"GO:0140619"}


id: PBO:0087990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-specific 2-thiouridylase; responsible for 2-thiolation of the wobble base of mitochondrial tRNAs; human homolog TRMU is implicated in myoclonus epilepsy associated with ragged red fibers (MERRF), and can complement yeast null mutant","termid":"PBO:0087990"}


id: GO:1904080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of transcription from RNA polymerase II promoter that is involved in neuron fate specification.","definition_xrefs":["PMID:11959845","GO_REF:0000060","GOC:kmv","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter involved in neuron fate specification (obsolete GO:1904080)","synonyms":[{"name":"activation of global transcription from RNA polymerase II promoter involved in neuron fate specification","type":"related"},{"name":"activation of transcription from RNA polymerase II promoter involved in neuron fate specification","type":"exact"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter involved in neuron fate specification","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter involved in neuron fate specification","type":"related"},{"name":"positive regulation of transcription from Pol II promoter involved in neuron fate specification","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter, global involved in neuron fate specification","type":"related"},{"name":"stimulation of global transcription from RNA polymerase II promoter involved in neuron fate specification","type":"narrow"},{"name":"stimulation of transcription from RNA polymerase II promoter involved in neuron fate specification","type":"exact"},{"name":"up regulation of global transcription from RNA polymerase II promoter involved in neuron fate specification","type":"related"},{"name":"up regulation of transcription from RNA polymerase II promoter involved in neuron fate specification","type":"exact"},{"name":"up-regulation of global transcription from RNA polymerase II promoter involved in neuron fate specification","type":"related"},{"name":"up-regulation of transcription from RNA polymerase II promoter involved in neuron fate specification","type":"exact"},{"name":"upregulation of global transcription from RNA polymerase II promoter involved in neuron fate specification","type":"related"},{"name":"upregulation of transcription from RNA polymerase II promoter involved in neuron fate specification","type":"exact"}],"termid":"GO:1904080"}


id: PBO:0004445
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NRde-Like","termid":"PBO:0004445"}


id: MOD:00699
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct with a compound containing a porphyrin group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"porphyrin modified residue","synonyms":[{"name":"PorphRes","type":"exact"}],"termid":"MOD:00699"}


id: PBO:0000190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein","termid":"PBO:0000190"}


id: GO:1905623
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of leaf development.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:11606552"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of leaf development","termid":"GO:2000024"},{"relation_name":"positively_regulates","term_name":"leaf development","termid":"GO:0048366"}],"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 leaf development","synonyms":[{"name":"activation of leaf development","type":"narrow"},{"name":"up regulation of leaf development","type":"exact"},{"name":"up-regulation of leaf development","type":"exact"},{"name":"upregulation of leaf development","type":"exact"}],"termid":"GO:1905623"}


id: PATO:0000375
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A distance which is lesser relative to the normal or average.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"distance","termid":"PATO:0000040"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased distance","synonyms":[{"name":"short distance","type":"related"}],"termid":"PATO:0000375"}


id: GO:0034856
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,4E)-2-hydroxyhexa-2,4-dienoate + H2O = 4-hydroxy-2-oxohexanoate.","definition_xrefs":["UM-BBD_reactionID:r1281"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"2-hydroxyhexa-2,4-dienoate hydratase activity","secondary_identifiers":["RHEA:32535","EC:4.2.1.132"],"termid":"GO:0034856"}


id: MONDO:0016650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paternal uniparental disomy of chromosome 1 is an uniparental disomy of paternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only father is a carrier.","definition_xrefs":["Orphanet:251004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 1 disorder","termid":"MONDO:0700008"},{"relation_name":"is_a","term_name":"uniparental disomy","termid":"MONDO:0700086"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paternal uniparental disomy of chromosome 1","secondary_identifiers":["SCTID:766719006","GARD:20688","icd11.foundation:1239235576","MEDGEN:1636519","UMLS:C4707800"],"synonyms":[{"name":"UPD(1)pat","type":"exact"},{"name":"paternal uniparental disomy of chromosome type 1","type":"exact"}],"termid":"MONDO:0016650","xrefs":{"Monarch":{"xref_id":"0016650"}}}


id: PBO:0074090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC26A5 antisense RNA 1","termid":"PBO:0074090"}


id: PBO:0076193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO2 pseudogene 2","termid":"PBO:0076193"}


id: PBO:0033774
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_maintenance_of_spindle_pole_body_localization","termid":"PBO:0033774"}


id: MONDO:0013197
data:
  {"annotated_genes":["SJAG_03703","SJAG_02431"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86783,86784],"is_not":false,"summary":null,"term":"MONDO:0013197"}]},"cv_name":"mondo","definition":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02431":null,"SJAG_03703":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"hypertrophic cardiomyopathy 14","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0110320","OMIM:613251","MEDGEN:442484","UMLS:C2750467","MESH:C567684"],"synonyms":[{"name":"CMH14","type":"exact"},{"name":"MYH6 hypertrophic cardiomyopathy","type":"exact"},{"name":"cardiomyopathy familial hypertrophic 14","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 14","type":"related"},{"name":"cardiomyopathy, familial hypertrophic, type 14","type":"exact"},{"name":"cardiomyopathy, hypertrophic, 14","type":"exact"},{"name":"hypertrophic cardiomyopathy caused by mutation in MYH6","type":"exact"},{"name":"hypertrophic cardiomyopathy type 14","type":"exact"}],"termid":"MONDO:0013197","terms_by_termid":{"MONDO:0013197":null},"xrefs":{"Monarch":{"xref_id":"0013197"}}}


id: GO:0004768
data:
  {"annotated_genes":["SJAG_03943"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75495],"is_not":false,"summary":null,"term":"GO:0004768"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 Fe(II)-[cytochrome b5] + 2 H+ + O2 + octadecanoyl-CoA = (9Z)-octadecenoyl-CoA + 2 Fe(III)-[cytochrome b5] + 2 H2O.","definition_xrefs":["RHEA:19721"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA desaturase activity","termid":"GO:0016215"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03943":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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"stearoyl-CoA 9-desaturase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0043735","EC:1.14.19.1","MetaCyc:1.14.19.1-RXN","Reactome:R-HSA-5690565","GO:0016214","Reactome:R-HSA-8847579"],"synonyms":[{"name":"acyl-CoA desaturase","type":"broad"},{"name":"delta(9)-desaturase activity","type":"broad"},{"name":"delta9-desaturase","type":"broad"},{"name":"fatty acid desaturase","type":"broad"},{"name":"stearoyl-CoA desaturase activity","type":"broad"}],"termid":"GO:0004768","terms_by_termid":{"GO:0004768":null}}


id: GO:0009148
data:
  {"annotated_genes":["SJAG_00533","SJAG_05024","SJAG_04627","SJAG_03708","SJAG_04665","SJAG_04657","SJAG_00885","SJAG_02887"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044210"},{"annotations":[64613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006241"},{"annotations":[68205,93295],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044211"},{"annotations":[71357,68976,92762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006235"},{"annotations":[107581],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009212"},{"annotations":[64612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006228"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of pyrimidine nucleoside triphosphate, a compound consisting of a pyrimidine base linked to a ribose or deoxyribose sugar esterified with triphosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate biosynthetic process","termid":"GO:0009142"},{"relation_name":"is_a","term_name":"pyrimidine nucleoside triphosphate metabolic process","termid":"GO:0009147"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00533":null,"SJAG_00885":null,"SJAG_02887":null,"SJAG_03708":null,"SJAG_04627":null,"SJAG_04657":null,"SJAG_04665":null,"SJAG_05024":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"pyrimidine nucleoside triphosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"pyrimidine nucleoside triphosphate anabolism","type":"exact"},{"name":"pyrimidine nucleoside triphosphate biosynthesis","type":"exact"},{"name":"pyrimidine nucleoside triphosphate formation","type":"exact"},{"name":"pyrimidine nucleoside triphosphate synthesis","type":"exact"}],"termid":"GO:0009148","terms_by_termid":{"GO:0006228":null,"GO:0006235":null,"GO:0006241":null,"GO:0009212":null,"GO:0044210":null,"GO:0044211":null}}


id: PBO:0054323
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 1716","termid":"PBO:0054323"}


id: MONDO:0004841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Global enlargement of the renal parenchyma in one or both kidneys.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"kidney hypertrophy","secondary_identifiers":["NCIT:C122991","DOID:9622","ICD9:593.1","ICD10CM:N28.81","MEDGEN:510218","SCTID:88531004","UMLS:C0156259"],"synonyms":[{"name":"hypertrophy of the kidney","type":"exact"},{"name":"renal Hypertrophy","type":"exact"}],"termid":"MONDO:0004841","xrefs":{"Monarch":{"xref_id":"0004841"}}}


id: PBO:0005718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fumarate hydratase (predicted)","termid":"PBO:0005718"}


id: PBO:0082466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calcium/H+ antiporter localized to the endoplasmic reticulum membrane; member of the calcium exchanger (CAX) family; potential Cdc28p substrate","termid":"PBO:0082466"}


id: PBO:0038885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADCY10 pseudogene 1","termid":"PBO:0038885"}


id: PATO:0000009
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000009 absolute speed (obsolete PATO:0000009)","termid":"PATO:0000009"}


id: MONDO:0017498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital absence of both forearm and hand, unilateral is a rare developmental defect during embryogenesis characterized by a unilateral, transverse absence of the radius and ulna (of varying terminal lengths), as well as all the elements composing the hand. Left or right side may be involved.","definition_xrefs":["Orphanet:295093"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital absence of both forearm and hand","termid":"MONDO:0017443"}],"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":"congenital absence of both forearm and hand, unilateral","secondary_identifiers":["icd11.foundation:2019491585"],"synonyms":[{"name":"radio-ulnar terminal transverse meromelia, unilateral","type":"exact"}],"termid":"MONDO:0017498","xrefs":{"Monarch":{"xref_id":"0017498"}}}


id: PBO:0072843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suppressor APC domain containing 1","termid":"PBO:0072843"}


id: MONDO:0022770
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":"circumscribed cutaneous aplasia of the vertex","termid":"MONDO:0022770","xrefs":{"Monarch":{"xref_id":"0022770"}}}


id: GO:1902914
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein polyubiquitination.","definition_xrefs":["GOC:di","GOC:TermGenie","GO_REF:0000058","PMID:23645667"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein ubiquitination","termid":"GO:0031396"},{"relation_name":"regulates","term_name":"protein polyubiquitination","termid":"GO:0000209"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"regulation of protein polyubiquitination","synonyms":[{"name":"regulation of polyubiquitin","type":"related"},{"name":"regulation of protein polyubiquitinylation","type":"exact"},{"name":"regulation of protein polyubiquitylation","type":"exact"}],"termid":"GO:1902914"}


id: PBO:0085489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Proline oxidase; nuclear-encoded mitochondrial protein involved in utilization of proline as sole nitrogen source; PUT1 transcription is induced by Put3p in the presence of proline and the absence of a preferred nitrogen source","termid":"PBO:0085489"}


id: PBO:0061216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein 8","termid":"PBO:0061216"}


id: PBO:0004109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b5 (predicted)","termid":"PBO:0004109"}


id: PR:Q10086
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- toe4 gene.","definition_xrefs":["UniProtKB:Q10086","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 transcriptional regulatory protein C11D3.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11D3.07c","synonyms":[{"name":"Spom972h-toe4","type":"exact"}],"termid":"PR:Q10086"}


id: PBO:0031279
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_meiotic_chromosome_segregation","termid":"PBO:0031279"}


id: PBO:0053072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipopolysaccharide binding protein","termid":"PBO:0053072"}


id: GO:0035666
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by a ligand binding to a toll-like receptor where the TRIF adaptor mediates transduction of the signal. Toll-like receptors directly bind pattern motifs from a variety of microbial sources to initiate an innate immune response.","definition_xrefs":["GOC:BHF","PMID:12855817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"MyD88-independent toll-like receptor signaling pathway","termid":"GO:0002756"}],"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:0008150","GO:0023052"],"is_obsolete":false,"name":"TRIF-dependent toll-like receptor signaling pathway","secondary_identifiers":["Reactome:R-HSA-937061","Reactome:R-HSA-9013973"],"synonyms":[{"name":"TRIF-dependent TLR signaling pathway","type":"exact"},{"name":"TRIF-dependent toll-like receptor signalling pathway","type":"exact"},{"name":"Toll/IL-1 receptor (TIR) domain-containing adaptor-dependent TLR signaling pathway","type":"exact"}],"termid":"GO:0035666"}


id: PBO:0066348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RCCD1 and UNC45A antisense RNA 1","termid":"PBO:0066348"}


id: PR:O94412
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A geranylgeranyl transferase type-2 subunit alpha that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11129:SF2"],"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":"geranylgeranyl transferase type-2 subunit alpha (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.05","secondary_identifiers":["UniProtKB:O94412"],"synonyms":[{"name":"GGTase-II-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PGGT (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPCC1620.05","type":"related"},{"name":"Spom972h-RABGGTA","type":"exact"},{"name":"geranylgeranyl transferase type II subunit alpha (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"type II protein geranyl-geranyltransferase subunit alpha (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94412"}


id: GO:0045856
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the process in which oskar mRNA is transported to, or maintained in, the oocyte pole plasm.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of pole plasm oskar mRNA localization","termid":"GO:0007317"},{"relation_name":"is_a","term_name":"positive regulation of intracellular mRNA localization","termid":"GO:1904582"},{"relation_name":"positively_regulates","term_name":"pole plasm oskar mRNA localization","termid":"GO:0045451"}],"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 pole plasm oskar mRNA localization","synonyms":[{"name":"activation of pole plasm oskar mRNA localization","type":"narrow"},{"name":"positive regulation of oocyte pole plasm oskar mRNA localization","type":"exact"},{"name":"positive regulation of pole plasm oskar mRNA localisation","type":"exact"},{"name":"stimulation of pole plasm oskar mRNA localization","type":"narrow"},{"name":"up regulation of pole plasm oskar mRNA localization","type":"exact"},{"name":"up-regulation of pole plasm oskar mRNA localization","type":"exact"},{"name":"upregulation of pole plasm oskar mRNA localization","type":"exact"}],"termid":"GO:0045856"}


id: PBO:0085493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Proposed gamma subunit of the heterotrimeric G protein; interacts with the receptor Gpr1p; involved in regulation of pseudohyphal growth; requires Gpb1p or Gpb2p to interact with Gpa2p; overproduction causes prion curing","termid":"PBO:0085493"}


id: GO:0016855
data:
  {"annotated_genes":["SJAG_00036","SJAG_04298"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62315,65767],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047661"}]},"cv_name":"molecular_function","definition":"Catalysis of a reaction that alters the configuration of one or more chiral centers in an amino acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity","termid":"GO:0016854"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00036":null,"SJAG_04298":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"racemase and epimerase activity, acting on amino acids and derivatives","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["EC:5.1.1.-"],"termid":"GO:0016855","terms_by_termid":{"GO:0047661":null}}


id: GO:0046660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment of the sex of a female organism by physical differentiation.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sex differentiation","termid":"GO:0007548"},{"relation_name":"part_of","term_name":"multicellular organism development","termid":"GO:0007275"}],"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 sex differentiation","termid":"GO:0046660"}


id: GO:0005694
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id: FYPO:0005004
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of a protein measured in the anaphase-promoting complex is lower than normal.","definition_xrefs":["PomBase:mah","PMID:22906049"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"},{"relation_name":"is_a","term_name":"abnormal protein complex composition","termid":"FYPO:0005003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein level in anaphase-promoting complex","synonyms":[{"name":"decreased anaphase-promoting complex protein level during vegetative growth","type":"exact"},{"name":"decreased protein level in APC","type":"exact"},{"name":"decreased protein level in anaphase-promoting complex during mitotic cell cycle","type":"related"},{"name":"decreased protein level in anaphase-promoting complex during vegetative growth","type":"exact"},{"name":"decreased protein level in cyclosome","type":"exact"},{"name":"reduced protein level in anaphase-promoting complex","type":"exact"}],"termid":"FYPO:0005004"}


id: MOD:01104
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-methoxy-2,3,6-trimethylbenzenesulfonyl","synonyms":[{"name":"Mtr","type":"exact"}],"termid":"MOD:01104"}


id: GO:0072279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The morphogenetic process in which the renal epithelium narrows along one axis and lengthens in a perpendicular axis that contributes to the shaping of a nephron in the metanephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"convergent extension involved in nephron morphogenesis","termid":"GO:0072045"},{"relation_name":"part_of","term_name":"metanephric nephron morphogenesis","termid":"GO:0072273"}],"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":"convergent extension involved in metanephric nephron morphogenesis","termid":"GO:0072279"}


id: MONDO:0033311
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome 33","secondary_identifiers":["DOID:0080279","OMIM:617767","UMLS:C4540389","MEDGEN:1615779"],"synonyms":[{"name":"JBTS33","type":"related"},{"name":"Joubert syndrome 33","type":"exact"}],"termid":"MONDO:0033311","xrefs":{"Monarch":{"xref_id":"0033311"}}}


id: MONDO:0043455
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypercalcemia generally develops as a late complication of malignancy; its appearance has grave prognostic significance. It remains unclear, however, whether death is associated with hypercalcemic crisis (uncontrolled or recurrent progressive hypercalcemia) or with advanced disease. Symptoms include central nervous system impairment such as delirium with prominent symptoms of personality change, cognitive dysfunction, disorientation, incoherent speech, and psychotic symptoms such as hallucinations and delusions, smooth muscle hypotonicity, and altered cardiovascular function.","definition_xrefs":["NCIT:C3496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypercalcemia disease","termid":"MONDO:0001566"},{"relation_name":"is_a","term_name":"paraneoplastic hematological syndrome","termid":"MONDO:0700253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005066"],"is_obsolete":false,"name":"humoral hypercalcemia of malignancy","secondary_identifiers":["MEDGEN:56210","SCTID:47709007","UMLS:C0149911","MESH:C562390"],"synonyms":[{"name":"hhm","type":"related"},{"name":"humoral hypercalcemia of malignancy","type":"exact"},{"name":"hypercalcemia of malignancy","type":"exact"},{"name":"mahc","type":"related"},{"name":"malignancy associated hypercalcemia","type":"related"},{"name":"malignant hypercalcemia","type":"related"}],"termid":"MONDO:0043455","xrefs":{"Monarch":{"xref_id":"0043455"}}}


id: PBO:0055996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long stress-induced non-coding transcript 5","termid":"PBO:0055996"}


id: PBO:0088926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMN complex subunit Gem7","termid":"PBO:0088926"}


id: PBO:0059628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier 2","termid":"PBO:0059628"}


id: GO:0034861
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: benzothiazole-2-sulfonate + H2O = 2-hydroxybenzothiazole + HSO3-.","definition_xrefs":["UM-BBD_reactionID:r1290"],"gene_count":0,"genotype_count":0,"name":"obsolete benzothiazole-2-sulfonate hydrolase activity (obsolete GO:0034861)","termid":"GO:0034861"}


id: FYPO:0003113
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 sodium nitroprusside 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:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0002682","FYPO:0001985","FYPO:0000139"],"is_obsolete":false,"name":"resistance to sodium nitroprusside","synonyms":[{"name":"resistance to sodium nitroprusside during mitotic cell cycle","type":"related"},{"name":"resistance to sodium nitroprusside during vegetative growth","type":"exact"},{"name":"resistant to sodium nitroprusside","type":"exact"}],"termid":"FYPO:0003113"}


id: MOD:01588
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-cholinephosphoryl-L-serine.","definition_xrefs":["PubMed:15249686","PubMed:16949362","RESID:AA0498","PubMed:16825186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-cholinephosphoryl-L-serine","synonyms":[{"name":"2-[([(2S)-2-amino-2-carboxyethoxy][hydroxy]phosphoryl)oxy]-N,N,N-trimethylethanaminium","type":"exact"},{"name":"2-[([(2S)-2-azanyl-2-carboxyethoxy][hydroxy]phosphoryl)oxy]-N,N,N-trimethylethanazanium","type":"exact"},{"name":"MOD_RES O-(2-cholinephosphoryl)serine","type":"exact"},{"name":"O-cholinephosphoryl-L-serine","type":"exact"},{"name":"O3-[(2-[trimethylammonio]ethyl)phosphoryl]-L-serine","type":"exact"},{"name":"O3-phosphocholine-L-serine","type":"exact"},{"name":"serine choline phosphate","type":"exact"},{"name":"serine choline phosphodiester","type":"exact"}],"termid":"MOD:01588"}


id: PR:P05767
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl39 gene.","definition_xrefs":["UniProtKB:P05767","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L39 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC663.04","synonyms":[{"name":"Spom972h-rpl39","type":"exact"},{"name":"YL36 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P05767"}


id: MONDO:0008351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pupil, egg-shaped (obsolete MONDO:0008351)","secondary_identifiers":["OMIM:178800","MESH:C566731"],"synonyms":[{"name":"egg shaped pupils","type":"related"},{"name":"ovoid pupils","type":"related"},{"name":"pupil, egg-shaped","type":"exact"}],"termid":"MONDO:0008351","xrefs":{"Monarch":{"xref_id":"0008351"}}}


id: GO:0031515
data:
  {"annotated_genes":["SJAG_02637","SJAG_02386"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[74381,75246],"is_not":false,"summary":null,"term":"GO:0031515"}]},"cv_name":"cellular_component","definition":"A protein complex involved in the catalysis of the formation of the modified nucleotide 1-methyladenosine (m1A) in tRNA. In yeast, it is a heterotetramer of two subunits, Gcd10p and Gcd14p, while in bacteria and archaea it is a homotetramer.","definition_xrefs":["PMID:10779558","PMID:14739239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA methyltransferase complex","termid":"GO:0043527"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02386":null,"SJAG_02637":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"tRNA (m1A) methyltransferase complex","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0031515","terms_by_termid":{"GO:0031515":null}}


id: GO:0032223
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cholinergic synaptic transmission, the process of communication from a neuron to another neuron across a synapse using the neurotransmitter acetylcholine.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synaptic transmission, cholinergic","termid":"GO:0032222"},{"relation_name":"is_a","term_name":"negative regulation of synaptic transmission","termid":"GO:0050805"},{"relation_name":"negatively_regulates","term_name":"synaptic transmission, cholinergic","termid":"GO:0007271"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of synaptic transmission, cholinergic","synonyms":[{"name":"down regulation of synaptic transmission, cholinergic","type":"exact"},{"name":"down-regulation of synaptic transmission, cholinergic","type":"exact"},{"name":"downregulation of synaptic transmission, cholinergic","type":"exact"},{"name":"inhibition of synaptic transmission, cholinergic","type":"narrow"}],"termid":"GO:0032223"}


id: PBO:0056568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucolipin TRP cation channel 3","termid":"PBO:0056568"}


id: PBO:0070644
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 15","termid":"PBO:0070644"}


id: GO:0003211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of a cardiac ventricle from unspecified parts. A cardiac ventricle receives blood from a cardiac atrium and pumps it out of the heart.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac chamber formation","termid":"GO:0003207"},{"relation_name":"part_of","term_name":"cardiac ventricle morphogenesis","termid":"GO:0003208"}],"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":"cardiac ventricle formation","termid":"GO:0003211"}


id: PBO:0055326
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 2754","termid":"PBO:0055326"}


id: PATO:0002017
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"magnitude","termid":"PATO:0002016"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased magnitude","synonyms":[{"name":"high magnitude","type":"exact"}],"termid":"PATO:0002017"}


id: GO:0033207
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the transfer of an N-acetylgalactosaminyl residue from UDP-N-acetyl-galactosamine to an acceptor molecule, forming a beta-1,4 linkage.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete beta-1,4-N-acetylgalactosaminyltransferase activity (obsolete GO:0033207)","synonyms":[{"name":"beta-1,4-GalNAc transferase activity","type":"exact"}],"termid":"GO:0033207"}


id: FYPO:0003189
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 protein import into the nucleus is decreased. Import of all proteins or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased nuclear import","termid":"FYPO:0000515"},{"relation_name":"is_a","term_name":"decreased protein transport during vegetative growth","termid":"FYPO:0000541"},{"relation_name":"is_a","term_name":"decreased protein localization to nucleus during vegetative growth","termid":"FYPO:0001514"},{"relation_name":"is_a","term_name":"abnormal protein import into nucleus during vegetative growth","termid":"FYPO:0003188"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein import into nucleus","synonyms":[{"name":"decreased protein import into nucleus during mitotic cell cycle","type":"related"},{"name":"decreased protein import into nucleus during vegetative growth","type":"exact"},{"name":"reduced protein import into nucleus","type":"exact"}],"termid":"FYPO:0003189"}


id: PBO:0030893
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cellular_response_to_starvation_during_vegetative_growth","termid":"PBO:0030893"}


id: PBO:0040995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BOLA3 divergent transcript","termid":"PBO:0040995"}


id: PBO:0110827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, zf-fungal binuclear cluster type, Toe1","termid":"PBO:0110827"}


id: PBO:0048091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin light chain pseudogene 12","termid":"PBO:0048091"}


id: PBO:0065751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PYDC2 antisense RNA 1","termid":"PBO:0065751"}


id: PR:Q9UTB0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC25B8.08 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTB0"],"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":"dilute domain-containing protein C25B8.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25B8.08","synonyms":[{"name":"Spom972h-SPAC25B8.08","type":"exact"}],"termid":"PR:Q9UTB0"}


id: PBO:0083166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; almost completely overlaps verified ORF MAK3/YPR051W","termid":"PBO:0083166"}


id: PBO:0055022
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 2437","termid":"PBO:0055022"}


id: PBO:0053688
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 881","termid":"PBO:0053688"}


id: PBO:0074868
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 52","termid":"PBO:0074868"}


id: PBO:0078335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon CTC) 1-7","termid":"PBO:0078335"}


id: PBO:0075470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis associated 20 pseudogene 1","termid":"PBO:0075470"}


id: MONDO:0030905
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"hearing loss, autosomal recessive 117","secondary_identifiers":["OMIM:619174","GARD:22665","MEDGEN:1747842","UMLS:C5436937"],"synonyms":[{"name":"DFNB117","type":"narrow"},{"name":"deafness, autosomal recessive 117","type":"narrow"}],"termid":"MONDO:0030905","xrefs":{"Monarch":{"xref_id":"0030905"}}}


id: PBO:0090777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear membrane organization protein Apq12","termid":"PBO:0090777"}


id: PBO:0075201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide G pseudogene 13","termid":"PBO:0075201"}


id: MONDO:0002744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare adenocarcinoma that arises from the fallopian tube. It is characterized by the presence of neoplastic epithelial cells that contain intracytoplasmic mucin. The cases that have been reported are predominantly in situ mucinous adenocarcinomas.","definition_xrefs":["NCIT:C40103"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube mucinous tumor","termid":"MONDO:0002745"},{"relation_name":"is_a","term_name":"fallopian tube adenocarcinoma","termid":"MONDO:0002746"},{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"}],"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":"fallopian tube mucinous adenocarcinoma","secondary_identifiers":["UMLS:C1517119","DOID:3704","MEDGEN:274489"],"synonyms":[{"name":"fallopian tube mucinous adenocarcinoma","type":"exact"}],"termid":"MONDO:0002744","xrefs":{"Monarch":{"xref_id":"0002744"}}}


id: PBO:0072720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoid X receptor gamma","termid":"PBO:0072720"}


id: RO:0002201
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of has phenotype","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phenotype_of","termid":"RO:0002201"}


id: PBO:0066038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAN pseudogene 7","termid":"PBO:0066038"}


id: GO:0016004
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases the activity of a phospholipase, an enzyme that catalyzes of the hydrolysis of a glycerophospholipid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipase activator activity","termid":"GO:0060229"},{"relation_name":"positively_regulates","term_name":"phospholipase activity","termid":"GO:0004620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"regulates","termid":"GO:0016787"},{"rel_name":"positively_regulates","termid":"GO:0016787"},{"rel_name":"positively_regulates","termid":"GO:0016788"},{"rel_name":"regulates","termid":"GO:0016788"},{"rel_name":"regulates","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"positively_regulates","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0030234","GO:0098772","GO:0003674","GO:0016788","GO:0140677","GO:0003824"],"is_obsolete":false,"name":"phospholipase activator activity","secondary_identifiers":["Reactome:R-HSA-400023"],"termid":"GO:0016004"}


id: MONDO:0014109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete NGLY1-deficiency (obsolete MONDO:0014109)","termid":"MONDO:0014109","xrefs":{"Monarch":{"xref_id":"0014109"}}}


id: PBO:0039613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annexin A2","termid":"PBO:0039613"}


id: PBO:0050130
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 40","termid":"PBO:0050130"}


id: PBO:0065177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PROP paired-like homeobox 1","termid":"PBO:0065177"}


id: GO:0004973
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete N-methyl-D-aspartate receptor-associated protein activity (obsolete GO:0004973)","synonyms":[{"name":"N-methyl-D-aspartate receptor-associated protein activity","type":"exact"}],"termid":"GO:0004973"}


id: MONDO:0010426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked endothelial corneal dystrophy (XECD) is a rare subtype of posterior corneal dystrophy characterized by congenital ground glass corneal clouding or a diffuse corneal haze, and blurred vision in male patients.","definition_xrefs":["Orphanet:293621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corneal endothelial dystrophy","termid":"MONDO:0000766"},{"relation_name":"is_a","term_name":"posterior corneal dystrophy","termid":"MONDO:0020214"}],"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":"X-linked endothelial corneal dystrophy","secondary_identifiers":["icd11.foundation:1842066261","UMLS:C2749049","SCTID:718579008","MESH:C567587","OMIM:300779","DOID:0060446","GARD:17339","MEDGEN:413518"],"synonyms":[{"name":"XECD","type":"exact"},{"name":"corneal dystrophy, endothelial, X-linked","type":"related"},{"name":"corneal dystrophy, endothelial, X-linked, X-linked dominant","type":"exact"},{"name":"endothelial corneal dystrophy, X-linked","type":"related"}],"termid":"MONDO:0010426","xrefs":{"Monarch":{"xref_id":"0010426"}}}


id: MONDO:0975756
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"benign vascular tumor","termid":"MONDO:0971115"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reactive angioendotheliomatosis","secondary_identifiers":["Orphanet:673574","MEDGEN:418935","UMLS:C2930870"],"termid":"MONDO:0975756","xrefs":{"Monarch":{"xref_id":"0975756"}}}


id: MONDO:0009697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lafora disease (LD) is a rare, inherited, severe, progressive myoclonic epilepsy characterized by myoclonus and/or generalized seizures, visual hallucinations (partial occipital seizures), and progressive neurological decline.","definition_xrefs":["Orphanet:501"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of glycogen metabolism","termid":"MONDO:0002412"},{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"progressive myoclonus epilepsy","termid":"MONDO:0020074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"Lafora disease","secondary_identifiers":["OMIMPS:254780","DOID:3534","MedDRA:10054030","MESH:D020192","NANDO:1200955","NANDO:2200881","NCIT:C84804","NORD:143373","UMLS:C0751783","GARD:8214","SCTID:230425004","MEDGEN:155631"],"synonyms":[{"name":"EPM2","type":"exact"},{"name":"Epm2","type":"related"},{"name":"Lafora body disease","type":"related"},{"name":"Lafora body disorder","type":"related"},{"name":"Lafora disease","type":"exact"},{"name":"Lafora progressive myoclonic epilepsy","type":"exact"},{"name":"Lafora's disease","type":"exact"},{"name":"Melf","type":"related"},{"name":"PME type 2","type":"exact"},{"name":"epilepsy progressive myoclonic 2","type":"related"},{"name":"epilepsy, progressive myoclonic 2A (Lafora)","type":"exact"},{"name":"epilepsy, progressive myoclonic 2B (Lafora)","type":"exact"},{"name":"epilepsy, progressive myoclonic, 2A","type":"related"},{"name":"epilepsy, progressive myoclonic, 2B","type":"related"},{"name":"myoclonic epilepsy of Lafora","type":"exact"},{"name":"progressive myoclonic epilepsy type 2","type":"exact"},{"name":"progressive myoclonus epilepsy type 2","type":"exact"}],"termid":"MONDO:0009697","xrefs":{"Monarch":{"xref_id":"0009697"}}}


id: PBO:0054801
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 2214","termid":"PBO:0054801"}


id: PBO:0079866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uracil-DNA glycosylase pseudogene 3","termid":"PBO:0079866"}


id: PBO:0044298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b5 type A","termid":"PBO:0044298"}


id: PBO:0039568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD62P1-PARP4P3 readthrough, transcribed pseudogene","termid":"PBO:0039568"}


id: GO:0022612
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a gland are generated and organized.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"},{"relation_name":"part_of","term_name":"gland development","termid":"GO:0048732"}],"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":"gland morphogenesis","termid":"GO:0022612"}


id: GO:0032993
data:
  {"annotated_genes":["SJAG_01873","SJAG_02362","SJAG_01523","SJAG_02074","SJAG_03451","SJAG_00272","SJAG_02098","SJAG_03941","SJAG_03543","SJAG_02627","SJAG_02194","SJAG_02818","SJAG_05979","SJAG_03855","SJAG_03685","SJAG_00303","SJAG_02172","SJAG_00857","SJAG_04210","SJAG_04062","SJAG_00874","SJAG_03120","SJAG_05197","SJAG_03722","SJAG_02667","SJAG_02182","SJAG_04341","SJAG_05239","SJAG_00814","SJAG_03206","SJAG_04994","SJAG_01762","SJAG_01267","SJAG_02800","SJAG_00302","SJAG_02348","SJAG_03780","SJAG_01010","SJAG_04995","SJAG_00729","SJAG_03092","SJAG_03942","SJAG_03542","SJAG_00536","SJAG_00696","SJAG_05301","SJAG_04245","SJAG_01378","SJAG_00335","SJAG_01354","SJAG_01624","SJAG_02607","SJAG_00884","SJAG_00327","SJAG_02394","SJAG_00863","SJAG_03927","SJAG_04877","SJAG_01864","SJAG_00307","SJAG_01777","SJAG_01698","SJAG_00336","SJAG_04150","SJAG_03047"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73187,75335,70754,75628],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005658"},{"annotations":[102380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043505"},{"annotations":[110697,63415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990879"},{"annotations":[77224,75360,103143,71366],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043625"},{"annotations":[80613,116576,77476],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005662"},{"annotations":[94258,77332,58437,72373,108146,111709,57159,111967,61125,66300,113891,61349,108364,74124,78510,113501,62811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031261"},{"annotations":[70671,80308,80642,79544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000811"},{"annotations":[119875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140573"},{"annotations":[113155,72925,76747,69171,77485,78012],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043599"},{"annotations":[61124,110885,62810,108149,72017,57158,61348,111712,111970,108367,74122,66299,103637,58436,113504],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005656"},{"annotations":[112840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043601"},{"annotations":[61038,74061,112930,77013,112902,112903,60374,73511,112931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000786"},{"annotations":[92159,116269,80117,95414,100042,90085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070187"},{"annotations":[108249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000782"},{"annotations":[70661,77873,77586],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097550"}]},"cv_name":"cellular_component","definition":"A macromolecular complex containing both protein and DNA molecules.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":65,"genes_by_uniquename":{"SJAG_00272":null,"SJAG_00302":null,"SJAG_00303":null,"SJAG_00307":null,"SJAG_00327":null,"SJAG_00335":null,"SJAG_00336":null,"SJAG_00536":null,"SJAG_00696":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00874":null,"SJAG_00884":null,"SJAG_01010":null,"SJAG_01267":null,"SJAG_01354":null,"SJAG_01378":null,"SJAG_01523":null,"SJAG_01624":null,"SJAG_01698":null,"SJAG_01762":null,"SJAG_01777":null,"SJAG_01864":null,"SJAG_01873":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02172":null,"SJAG_02182":null,"SJAG_02194":null,"SJAG_02348":null,"SJAG_02362":null,"SJAG_02394":null,"SJAG_02607":null,"SJAG_02627":null,"SJAG_02667":null,"SJAG_02800":null,"SJAG_02818":null,"SJAG_03047":null,"SJAG_03092":null,"SJAG_03120":null,"SJAG_03206":null,"SJAG_03451":null,"SJAG_03542":null,"SJAG_03543":null,"SJAG_03685":null,"SJAG_03722":null,"SJAG_03780":null,"SJAG_03855":null,"SJAG_03927":null,"SJAG_03941":null,"SJAG_03942":null,"SJAG_04062":null,"SJAG_04150":null,"SJAG_04210":null,"SJAG_04245":null,"SJAG_04341":null,"SJAG_04877":null,"SJAG_04994":null,"SJAG_04995":null,"SJAG_05197":null,"SJAG_05239":null,"SJAG_05301":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"protein-DNA complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:24184107":null},"synonyms":[{"name":"DNA-protein complex","type":"exact"}],"termid":"GO:0032993","terms_by_termid":{"GO:0000782":null,"GO:0000786":null,"GO:0000811":null,"GO:0005656":null,"GO:0005658":null,"GO:0005662":null,"GO:0031261":null,"GO:0043505":null,"GO:0043599":null,"GO:0043601":null,"GO:0043625":null,"GO:0070187":null,"GO:0097550":null,"GO:0140573":null,"GO:1990879":null}}


id: MONDO:0035349
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A localized form of dystrophic epidermolysis bullosa characterized by blisters confined primarily to the hands and feet (acral form) or to the pretibial region (pretibial form). Nail dystrophy or loss is common and may be an isolated finding (nail only form). This disease can be inherited via autosomal dominant or autosomal recessive inheritance.","definition_xrefs":["Orphanet:595356"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa dystrophica","termid":"MONDO:0006543"}],"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":"localized dystrophic epidermolysis bullosa","secondary_identifiers":["MEDGEN:634276","GARD:22388","UMLS:C0474885"],"synonyms":[{"name":"localised DEB","type":"exact"},{"name":"localized DEB","type":"exact"}],"termid":"MONDO:0035349","xrefs":{"Monarch":{"xref_id":"0035349"}}}


id: PBO:0112990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Actin, structural protein in cytoskeleton; involved in cell polarization, endocytosis, and other cytoskeletal functions; monomeric actin in the nucleus plays a role in INO80 chromatin remodeling","termid":"PBO:0112990"}


id: PBO:0011436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retrotransposable element/transposon Tf2-type","termid":"PBO:0011436"}


id: GO:0005947
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Mitochondrial complex that possesses alpha-ketoglutarate dehydrogenase activity.","definition_xrefs":["GOC:mah","GOC:mtg_sensu"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial alpha-ketoglutarate dehydrogenase complex (obsolete GO:0005947)","synonyms":[{"name":"2-oxoglutarate dehydrogenase complex","type":"broad"}],"termid":"GO:0005947"}


id: MONDO:0000230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infectious disease caused by infection with rickettsia conorii subsp. israelensis.","definition_xrefs":["PMID:18760001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Rickettsia conorii infectious disease","termid":"MONDO:0005677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Israeli tick typhus","secondary_identifiers":["DOID:0050043"],"synonyms":[{"name":"Israeli spotted fever","type":"related"}],"termid":"MONDO:0000230","xrefs":{"Monarch":{"xref_id":"0000230"}}}


id: GO:0035506
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of myosin light chain kinase activity.","definition_xrefs":["GOC:bf","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of myosin light chain kinase activity (obsolete GO:0035506)","termid":"GO:0035506"}


id: PR:P57728
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl2801 gene.","definition_xrefs":["UniProtKB:P57728","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L28-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC776.11","synonyms":[{"name":"Spom972h-rpl2801","type":"exact"}],"termid":"PR:P57728"}


id: MONDO:0016606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Prenatal benign hypophosphatasia (PB-HPP) is a very rare form of hypophosphatasia characterized by prenatal skeletal manifestations (limb shortening and bowing) that slowly resolve spontaneously and later develop into the milder infantile, childhood or adult forms of the disease.","definition_xrefs":["Orphanet:247638"],"gene_count":0,"genotype_count":0,"name":"obsolete prenatal benign hypophosphatasia (obsolete MONDO:0016606)","secondary_identifiers":["ICD10CM:E83.3"],"synonyms":[{"name":"prenatal benign Rathburn disease","type":"exact"},{"name":"prenatal benign phosphoethanolaminuria","type":"exact"}],"termid":"MONDO:0016606","xrefs":{"Monarch":{"xref_id":"0016606"}}}


id: GO:0031375
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.","definition_xrefs":["ISBN:0471331309","PMID:12957385","ISBN:0716720094","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete type II fatty acid synthase complex (obsolete GO:0031375)","synonyms":[{"name":"type II FAS","type":"exact"},{"name":"type II FAS complex","type":"exact"},{"name":"type II fatty acid synthase","type":"exact"},{"name":"type II fatty acid synthase complex","type":"exact"}],"termid":"GO:0031375"}


id: PBO:0068335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 43","termid":"PBO:0068335"}


id: PBO:0087303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SKI complex-associated protein; involved in 3'-5' degradation of long 3'UTR-containing mRNA, poorly translated mRNA, and other RNA regions devoid of ribosomes; proposed to assist the cytoplasmic exosome in a Ska1-SKI complex when a direct interaction between the ribosome and the SKI complex is absent","termid":"PBO:0087303"}


id: FYPO:0003679
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to epirubicin. Cells stop growing (and may die) at a concentration of epirubicin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0001985","FYPO:0002683","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to epirubicin","synonyms":[{"name":"hypersensitive to epirubicin","type":"exact"},{"name":"sensitive to 4'-epidoxorubicin","type":"exact"},{"name":"sensitive to epirubicin during mitotic cell cycle","type":"related"},{"name":"sensitive to epirubicin during vegetative growth","type":"exact"}],"termid":"FYPO:0003679"}


id: GO:0005701
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A region at which the centric regions of polytene chromosomes are joined together.","definition_xrefs":["GOC:bf","ISBN:0120649012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromocenter","termid":"GO:0010369"},{"relation_name":"part_of","term_name":"polytene chromosome","termid":"GO:0005700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0005575"],"is_obsolete":false,"name":"polytene chromosome chromocenter","synonyms":[{"name":"polytene chromosome chromocentre","type":"exact"}],"termid":"GO:0005701"}


id: PR:C6Y4C1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pet117 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4C1"],"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 pet117, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.25","synonyms":[{"name":"Spom972h-pet117","type":"exact"}],"termid":"PR:C6Y4C1"}


id: GO:0060896
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process that results in the creation of defined areas or spaces within the neural plate to which cells respond and eventually are instructed to differentiate.","definition_xrefs":["GOC:tb","GOC:sdb_2009","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification process","termid":"GO:0007389"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural plate pattern specification","secondary_identifiers":["Reactome:R-HSA-9834899"],"termid":"GO:0060896"}


id: GO:0008842
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: diphosphate + a purine nucleoside = monophosphate + a purine mononucleotide.","definition_xrefs":["GOC:rynl"],"gene_count":0,"genotype_count":0,"name":"obsolete diphosphate-purine nucleoside kinase activity (obsolete GO:0008842)","termid":"GO:0008842"}


id: MONDO:0003936
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive adenocarcinoma of the breast with a favorable prognosis. It is composed of tubular structures lined by a single layer of epithelium.","definition_xrefs":["NCIT:C9135"],"direct_ancestors":[{"relation_name":"is_a","term_name":"invasive ductal breast carcinoma","termid":"MONDO:0004953"},{"relation_name":"is_a","term_name":"tubular adenocarcinoma","termid":"MONDO:0005606"}],"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":"invasive tubular breast carcinoma","secondary_identifiers":["DOID:6587","UMLS:C1328544","MEDGEN:230969"],"synonyms":[{"name":"breast tubular adenocarcinoma","type":"exact"},{"name":"infiltrating tubular breast carcinoma","type":"exact"},{"name":"infiltrating tubular carcinoma of breast","type":"exact"},{"name":"infiltrating tubular carcinoma of the breast","type":"exact"},{"name":"invasive tubular breast carcinoma","type":"exact"},{"name":"invasive tubular carcinoma of breast","type":"exact"},{"name":"invasive tubular carcinoma of the breast","type":"exact"},{"name":"tubular breast cancer","type":"exact"},{"name":"tubular breast carcinoma","type":"exact"},{"name":"tubular carcinoma of breast","type":"exact"},{"name":"tubular carcinoma of the breast","type":"exact"}],"termid":"MONDO:0003936","xrefs":{"Monarch":{"xref_id":"0003936"}}}


id: GO:0021842
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation and reception of signals that result in the movement of interneurons away from the signal during migration from the subpallium to the cortex.","definition_xrefs":["GOC:dgh","GO_REF:0000021","GOC:dph","GOC:cls","GOC:jid","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative chemotaxis","termid":"GO:0050919"},{"relation_name":"part_of","term_name":"directional guidance of interneurons involved in migration from the subpallium to the cortex","termid":"GO:0021840"}],"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 interneuron migration from the subpallium to the cortex","synonyms":[{"name":"negative chemotaxis involved in interneuron migration from the subpallium to the cortex","type":"exact"}],"termid":"GO:0021842"}


id: GO:1990890
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a netrin receptor.","definition_xrefs":["PMID:9126742","PMID:8861902","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"netrin receptor binding","termid":"GO:1990890"}


id: PBO:0058787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7156","termid":"PBO:0058787"}


id: GO:0009866
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by ethylene (ethene) involved in induced systemic resistance.","definition_xrefs":["GOC:jy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activation of innate immune response","termid":"GO:0002218"},{"relation_name":"is_a","term_name":"immune effector process","termid":"GO:0002252"},{"relation_name":"is_a","term_name":"ethylene-activated signaling pathway","termid":"GO:0009873"},{"relation_name":"part_of","term_name":"induced systemic resistance","termid":"GO:0009682"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"induced systemic resistance, ethylene mediated signaling pathway","synonyms":[{"name":"ethene mediated signaling pathway (induced systemic resistance)","type":"exact"},{"name":"ethylene mediated signaling pathway (induced systemic resistance)","type":"exact"},{"name":"induced systemic resistance, ethene mediated signaling pathway","type":"exact"},{"name":"induced systemic resistance, ethene mediated signalling pathway","type":"exact"},{"name":"induced systemic resistance, ethylene mediated signalling pathway","type":"exact"}],"termid":"GO:0009866"}


id: SO:0001248
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of the genome of known length that is composed by ordering and aligning two or more different regions.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"experimental_feature","termid":"SO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"assembly","secondary_identifiers":["http://en.wikipedia.org/wiki/Genome_assembly#Genome_assembly"],"termid":"SO:0001248"}


id: GO:0018606
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: toluene-4-sulfonate + NADH + O2 + H+ = NAD+ + HSO3(-) + 4-methylcatechol.","definition_xrefs":["UM-BBD_reactionID:r0295"],"gene_count":0,"genotype_count":0,"name":"obsolete benzenesulfonate dioxygenase activity (obsolete GO:0018606)","synonyms":[{"name":"benzenesulphonate dioxygenase activity","type":"exact"}],"termid":"GO:0018606"}


id: MONDO:0020365
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital hereditary endothelial dystrophy I (CHED I) is a rare subtype of posterior corneal dystrophy characterized by a diffuse ground-glass appearance of the corneas and marked corneal thickening from birth or infancy without nystagmus, with blurred vision.","definition_xrefs":["Orphanet:98975"],"direct_ancestors":[{"relation_name":"is_a","term_name":"posterior corneal dystrophy","termid":"MONDO:0020214"}],"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":"congenital hereditary endothelial dystrophy type I","secondary_identifiers":["UMLS:C1562945","MEDGEN:736888","GARD:19610","OMIM:121700","SCTID:416633008"],"synonyms":[{"name":"CHED1","type":"exact"},{"name":"CHEDI","type":"exact"},{"name":"autosomal dominant CHED","type":"exact"},{"name":"autosomal dominant congenital hereditary endothelial dystrophy","type":"exact"},{"name":"congenital hereditary endothelial dystrophy type 1","type":"exact"}],"termid":"MONDO:0020365","xrefs":{"Monarch":{"xref_id":"0020365"}}}


id: PBO:0071875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 13","termid":"PBO:0071875"}


id: MONDO:0002220
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tooth disorder","termid":"MONDO:0006999"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tooth hard tissue disease","secondary_identifiers":["UMLS:C0155926","ICD9:521.89","ICD10CM:K03","MEDGEN:510140","DOID:214","SCTID:46557008","ICD9:521.8"],"synonyms":[{"name":"disorder of hard tissues of teeth","type":"exact"},{"name":"teeth hard tissue disease","type":"related"},{"name":"teeth hard tissue diseases","type":"related"}],"termid":"MONDO:0002220","xrefs":{"Monarch":{"xref_id":"0002220"}}}


id: GO:0030279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of ossification, the formation of bone or of a bony substance or the conversion of fibrous tissue or of cartilage into bone or a bony substance.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ossification","termid":"GO:0030278"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"ossification","termid":"GO:0001503"}],"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 ossification","synonyms":[{"name":"down regulation of ossification","type":"exact"},{"name":"down-regulation of ossification","type":"exact"},{"name":"downregulation of ossification","type":"exact"},{"name":"inhibition of ossification","type":"narrow"},{"name":"negative regulation of bone biosynthesis","type":"exact"},{"name":"negative regulation of bone formation","type":"exact"}],"termid":"GO:0030279"}


id: MONDO:0001453
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral retinal degeneration","termid":"MONDO:0001451"}],"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":"senile reticular retinal degeneration","secondary_identifiers":["ICD9:362.64","UMLS:C0154857","MEDGEN:509687","SCTID:54184008","DOID:12163"],"synonyms":[{"name":"Senile reticular degeneration of retina","type":"exact"}],"termid":"MONDO:0001453","xrefs":{"Monarch":{"xref_id":"0001453"}}}


id: PBO:0056229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member L2","termid":"PBO:0056229"}


id: MONDO:1010052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes mellitus that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"},{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"},{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetes mellitus, non-human animal","secondary_identifiers":["OMIA:000279"],"termid":"MONDO:1010052","xrefs":{"Monarch":{"xref_id":"1010052"}}}


id: PBO:0112882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial 2-oxoglutarate dehydrogenase (lipoamide) (e1 component of oxoglutarate dehydrogenase complex), Kgd1","termid":"PBO:0112882"}


id: GO:0021614
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for the glossopharyngeal nerve to attain its fully functional state. Various sensory and motor branches of the glossopharyngeal nerve supply nerve connections to the pharynx and back of the tongue. The branchial motor component contains motor fibers that innervate muscles that elevate the pharynx and larynx, and the tympanic branch supplies parasympathetic fibers to the otic ganglion.","definition_xrefs":["GOC:jid","ISBN:0838580343","GO_REF:0000021","GOC:dgh","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve maturation","termid":"GO:0021605"},{"relation_name":"part_of","term_name":"glossopharyngeal nerve development","termid":"GO:0021563"}],"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":"glossopharyngeal nerve maturation","synonyms":[{"name":"CN IX maturation","type":"related"}],"termid":"GO:0021614"}


id: PBO:0042507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin related family member 1","termid":"PBO:0042507"}


id: GO:0031758
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an Edg-5 sphingosine 1-phosphate receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial differentiation G protein-coupled receptor binding","termid":"GO:0031753"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"Edg-5 sphingosine 1-phosphate receptor binding","synonyms":[{"name":"Edg-5 sphingosine 1-phosphate receptor ligand","type":"narrow"}],"termid":"GO:0031758"}


id: MONDO:0100205
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with parainfluenza virus type 4.","definition_xrefs":["PMID:21636318","MONDO:patterns/infectious_disease_by_agent","PMID:27197630"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parainfluenza infectious disease","termid":"MONDO:0100197"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parainfluenza virus type 4 infectious disease","synonyms":[{"name":"human rubulavirus 4 infectious disease","type":"exact"},{"name":"infection caused by human parainfluenza virus 4","type":"exact"},{"name":"infection caused by parainfluenza virus 4","type":"related"},{"name":"infection due to human parainfluenza virus 4","type":"exact"},{"name":"infection due to parainfluenza virus 4","type":"related"}],"termid":"MONDO:0100205","xrefs":{"Monarch":{"xref_id":"0100205"}}}


id: PBO:0027667
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_chromatin_silencing","termid":"PBO:0027667"}


id: PBO:0029559
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_cilofungin","termid":"PBO:0029559"}


id: GO:0006114
data:
  {"annotated_genes":["SJAG_00409","SJAG_01012"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94301,106827],"is_not":false,"summary":null,"term":"GO:0006114"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glycerol, 1,2,3-propanetriol, a sweet, hygroscopic, viscous liquid, widely distributed in nature as a constituent of many lipids.","definition_xrefs":["GOC:ai","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerol metabolic process","termid":"GO:0006071"},{"relation_name":"is_a","term_name":"alditol biosynthetic process","termid":"GO:0019401"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00409":null,"SJAG_01012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"glycerol biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"glycerol anabolism","type":"exact"},{"name":"glycerol biosynthesis","type":"exact"},{"name":"glycerol formation","type":"exact"},{"name":"glycerol synthesis","type":"exact"}],"termid":"GO:0006114","terms_by_termid":{"GO:0006114":null}}


id: PBO:0086921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative Zn(II)2Cys6 motif containing transcription factor; non-essential gene identified in a screen for mutants with increased levels of rDNA transcription; similar to S. kluyveri Urc2p involved in uracil catabolism","termid":"PBO:0086921"}


id: GO:0141162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cAMP/PKA signal transduction.","definition_xrefs":["PMID:17376027"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cAMP/PKA signal transduction","termid":"GO:0141161"},{"relation_name":"is_a","term_name":"negative regulation of intracellular signal transduction","termid":"GO:1902532"},{"relation_name":"negatively_regulates","term_name":"cAMP/PKA signal transduction","termid":"GO:0141156"}],"gene_count":0,"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:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of cAMP/PKA signal transduction","synonyms":[{"name":"negative regulation of cAMP/PKA signaling","type":"exact"}],"termid":"GO:0141162"}


id: PBO:0057878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3182","termid":"PBO:0057878"}


id: MONDO:0010034
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete anosmia for butyl mercaptan (obsolete MONDO:0010034)","secondary_identifiers":["OMIM:270350"],"synonyms":[{"name":"skunk N-BUTYLMERCAPTAN, inability to smell","type":"related"},{"name":"skunk N-butyl mercaptan, inability to smell","type":"related"}],"termid":"MONDO:0010034","xrefs":{"Monarch":{"xref_id":"0010034"}}}


id: MOD:01566
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ8plex-118 reporter+balance group.","definition_xrefs":["Unimod:731#Y"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"},{"relation_name":"is_a","term_name":"iTRAQ8plex-118 reporter+balance reagent acylated residue","termid":"MOD:01563"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent O-acylated residue","termid":"MOD:01714"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-118 reporter+balance reagent O4'-acylated tyrosine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Accurate mass for 115, 118, 119 & 121","type":"related"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"iTRAQ8plex:13C(6)15N(2)","type":"related"}],"termid":"MOD:01566"}


id: PBO:0068030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 335","termid":"PBO:0068030"}


id: PBO:0081856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 789","termid":"PBO:0081856"}


id: PBO:0012265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino acid transporter Aat1","termid":"PBO:0012265"}


id: PBO:0081851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 784","termid":"PBO:0081851"}


id: PBO:0065784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamine and serine rich 1","termid":"PBO:0065784"}


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


id: FYPO:0003308
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the mitotic spindle pole body is normal (i.e. indistinguishable from wild type) during interphase of the cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to mitotic spindle pole body","termid":"FYPO:0002967"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0000138","FYPO:0001312"],"is_obsolete":false,"name":"normal protein localization to mitotic spindle pole body during interphase","synonyms":[{"name":"normal protein localisation to mitotic spindle pole body during interphase","type":"exact"},{"name":"normal protein localization to mitotic SPB during interphase","type":"exact"},{"name":"normal protein localization to mitotic spindle pole body during mitotic interphase","type":"exact"},{"name":"normal protein localization to spindle pole body during interphase during vegetative growth","type":"exact"}],"termid":"FYPO:0003308"}


id: PBO:0040766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BEN domain containing 3 pseudogene 1","termid":"PBO:0040766"}


id: MONDO:0100249
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"46,XX testicular disorder of sex development (46,XX testicular DSD) is characterized by male external genitalia, ranging from normal to ambiguous with associated testosterone deficiency.","definition_xrefs":["Orphanet:393"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"46 XX gonadal dysgenesis","termid":"MONDO:0009299"},{"relation_name":"is_a","term_name":"46,XX disorder of sex development","termid":"MONDO:0017576"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"46,XX testicular disorder of sex development","secondary_identifiers":["UMLS:C2936419","MEDGEN:424734","MESH:D058531","DOID:0111760","GARD:399","icd11.foundation:1357942532","NCIT:C127170"],"synonyms":[{"name":"46, XX gonadal sex reversal","type":"related"},{"name":"46,XX testicular DSD","type":"exact"},{"name":"46,XX testicular differences of sex development","type":"exact"},{"name":"46,XX testicular disorder of sex development","type":"exact"},{"name":"46,XX testicular disorders of Sex development","type":"exact"},{"name":"De la Chapelle syndrome","type":"exact"},{"name":"XX Male, Sry-positive","type":"related"},{"name":"XX male syndrome","type":"related"},{"name":"XX sex reversal","type":"related"},{"name":"XX, male syndrome","type":"exact"}],"termid":"MONDO:0100249","xrefs":{"Monarch":{"xref_id":"0100249"}}}


id: GO:0050709
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the controlled release of a protein from a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein secretion","termid":"GO:0050708"},{"relation_name":"is_a","term_name":"negative regulation of protein transport","termid":"GO:0051224"},{"relation_name":"is_a","term_name":"negative regulation of secretion by cell","termid":"GO:1903531"},{"relation_name":"negatively_regulates","term_name":"protein secretion","termid":"GO:0009306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of protein secretion","synonyms":[{"name":"down regulation of protein secretion","type":"exact"},{"name":"down-regulation of protein secretion","type":"exact"},{"name":"downregulation of protein secretion","type":"exact"},{"name":"inhibition of protein secretion","type":"narrow"}],"termid":"GO:0050709"}


id: GO:0002441
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of histamine by a cell as part of an inflammatory response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histamine secretion","termid":"GO:0001821"},{"relation_name":"is_a","term_name":"hormone secretion","termid":"GO:0046879"},{"relation_name":"part_of","term_name":"histamine production involved in inflammatory response","termid":"GO:0002349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"histamine secretion involved in inflammatory response","synonyms":[{"name":"histamine secretion involved in acute inflammatory response","type":"broad"}],"termid":"GO:0002441"}


id: MONDO:1010557
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spina bifida that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spina bifida, non-human animal","termid":"MONDO:1010047"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spina bifida, domestic cat","secondary_identifiers":["OMIA:000933-9685"],"termid":"MONDO:1010557","xrefs":{"Monarch":{"xref_id":"1010557"}}}


id: PBO:0063424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphodiesterase 4C","termid":"PBO:0063424"}


id: FYPO:0004504
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 proteasome localization is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal proteasome localization","synonyms":[{"name":"normal proteasome localisation","type":"exact"},{"name":"normal proteasome localization during mitotic cell cycle","type":"related"},{"name":"normal proteasome localization during vegetative growth","type":"exact"},{"name":"normal proteasome location","type":"related"}],"termid":"FYPO:0004504"}


id: PBO:0114087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F1-FO ATP synthase subunit H /peripheral stalk subunit F6, Atp14","termid":"PBO:0114087"}


id: PBO:0058391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4763","termid":"PBO:0058391"}


id: FYPO:0005817
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 one or both ends end of a microtubule does not occur during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to microtubule during mitotic interphase","termid":"FYPO:0005441"},{"relation_name":"is_a","term_name":"abolished protein localization to microtubule plus-end","termid":"FYPO:0005814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to microtubule plus-end during mitotic interphase","synonyms":[{"name":"abolished protein localisation to microtubule plus-end during mitotic interphase","type":"exact"},{"name":"abolished protein localization to microtubule plus end during mitotic interphase","type":"exact"},{"name":"abolished protein localization to microtubule plus-end during interphase during vegetative growth","type":"exact"},{"name":"abolished protein localization to microtubule plus-end during interphase of mitotic cell cycle","type":"exact"},{"name":"protein localization to microtubule plus-end abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0005817"}


id: PR:Q09874
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC12G12.11c gene.","definition_xrefs":["UniProtKB:Q09874","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 C12G12.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC12G12.11c","synonyms":[{"name":"Spom972h-SPAC12G12.11c","type":"exact"}],"termid":"PR:Q09874"}


id: GO:0035635
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a bacterium enters a host cell. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:21187937","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont entry into host","termid":"GO:0044409"}],"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":"entry of bacterium into host cell","synonyms":[{"name":"bacterial entry into host cell","type":"exact"},{"name":"invasion of bacteria into host cell","type":"exact"}],"termid":"GO:0035635"}


id: MONDO:1011003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polymicrogyria that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polymicrogyria, non-human animal","termid":"MONDO:1010237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polymicrogyria, cattle","secondary_identifiers":["OMIA:001100-9913"],"termid":"MONDO:1011003","xrefs":{"Monarch":{"xref_id":"1011003"}}}


id: PBO:0013785
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements E. coli MutY","termid":"PBO:0013785"}


id: PBO:0071559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 24","termid":"PBO:0071559"}


id: PBO:0062415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 46 pseudogene","termid":"PBO:0062415"}


id: GO:1903136
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a cuprous ion, copper(1+).","definition_xrefs":["GOC:bf","PMID:24567322","GOC:PARL","GO_REF:0000067","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copper ion binding","termid":"GO:0005507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0046872"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0046872","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"cuprous ion binding","synonyms":[{"name":"Cu(+) binding","type":"exact"},{"name":"Cu(I) binding","type":"exact"},{"name":"copper(1+) binding","type":"exact"}],"termid":"GO:1903136"}


id: MONDO:0019060
data:
  {"annotated_genes":["SJAG_01151","SJAG_03881","SJAG_01748","SJAG_01013","SJAG_03905","SJAG_05979","SJAG_03453","SJAG_01349","SJAG_04287","SJAG_02855","SJAG_03429"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87531,87685,87532,87530,87529,87684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"},{"annotations":[86490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0002629"},{"annotations":[85658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"},{"annotations":[87055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"},{"annotations":[87114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007205"},{"annotations":[85993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007767"},{"annotations":[85994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007768"}]},"cv_name":"mondo","definition":"A benign, intermediate, or malignant neoplasm involving the bone or articular cartilage.","definition_xrefs":["NCIT:C9343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"},{"relation_name":"is_a","term_name":"connective tissue neoplasm","termid":"MONDO:0021581"}],"gene_count":11,"genes_by_uniquename":{"SJAG_01013":null,"SJAG_01151":null,"SJAG_01349":null,"SJAG_01748":null,"SJAG_02855":null,"SJAG_03429":null,"SJAG_03453":null,"SJAG_03881":null,"SJAG_03905":null,"SJAG_04287":null,"SJAG_05979":null},"genotype_count":0,"is_obsolete":false,"name":"bone neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:68411","UMLS:C2732838","EFO:0003820","ONCOTREE:BONE","GARD:18892","MEDGEN:488993","ICD10CM:C40-C41"],"synonyms":[{"name":"bone neoplasm","type":"exact"},{"name":"bone neoplasms","type":"exact"},{"name":"bone tissue neoplasm","type":"exact"},{"name":"bone tissue tumor","type":"exact"},{"name":"bone tissue tumour","type":"exact"},{"name":"bone tumor","type":"exact"},{"name":"bone tumors","type":"exact"},{"name":"bone tumour","type":"exact"},{"name":"bone tumours","type":"exact"},{"name":"neoplasm of bone","type":"exact"},{"name":"neoplasm of bone tissue","type":"exact"},{"name":"neoplasm of the bone","type":"exact"},{"name":"osseous neoplasm","type":"exact"},{"name":"osseous tumor","type":"exact"},{"name":"osseous tumour","type":"exact"},{"name":"primary bone cancer","type":"related"},{"name":"primary malignant neoplasm of bone","type":"related"},{"name":"rare bone tumor","type":"related"},{"name":"rare bone tumour","type":"related"},{"name":"tumor of bone","type":"exact"},{"name":"tumor of bone tissue","type":"exact"},{"name":"tumor of the bone","type":"exact"},{"name":"tumour of bone","type":"exact"},{"name":"tumour of bone tissue","type":"exact"},{"name":"tumour of the bone","type":"exact"}],"termid":"MONDO:0019060","terms_by_termid":{"MONDO:0002629":null,"MONDO:0007205":null,"MONDO:0007767":null,"MONDO:0007768":null,"MONDO:0009050":null,"MONDO:0010621":null,"MONDO:0018874":null},"xrefs":{"Monarch":{"xref_id":"0019060"}}}


id: GO:0000437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transcription regulation process in which the presence of one carbon source leads to a decrease in the frequency, rate, or extent of transcription, from an RNA polymerase II promoter, of specific genes involved in the metabolism of other carbon sources.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transcription by RNA polymerase II","termid":"GO:0000122"},{"relation_name":"is_a","term_name":"carbon catabolite regulation of transcription from RNA polymerase II promoter","termid":"GO:0000429"},{"relation_name":"is_a","term_name":"carbon catabolite repression of transcription","termid":"GO:0045013"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0006351","GO:0006355","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"carbon catabolite repression of transcription from RNA polymerase II promoter","synonyms":[{"name":"negative regulation of transcription from RNA polymerase II promoter by carbon catabolites","type":"exact"}],"termid":"GO:0000437"}


id: GO:0001922
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of regulating the proliferation and elimination of B cells of the B-1 subset such that the total number of B-1 B cells within a whole or part of an organism is stable over time in the absence of an outside stimulus. B-1 B cells are a distinct subset of B cells characterized as being CD5 positive, found predominantly in the peritoneum, pleural cavities, and spleen, and enriched for self-reactivity.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell homeostasis","termid":"GO:0001782"}],"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":"B-1 B cell homeostasis","synonyms":[{"name":"B-1 B lymphocyte homeostasis","type":"exact"},{"name":"B-1 B-cell homeostasis","type":"exact"},{"name":"B-1 B-lymphocyte homeostasis","type":"exact"}],"termid":"GO:0001922"}


id: PBO:0078164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 41","termid":"PBO:0078164"}


id: GO:0008660
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-aminocyclopropane-1-carboxylate + H2O = 2-oxobutanate + NH4.","definition_xrefs":["RHEA:16933"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787","GO:0016810"],"is_obsolete":false,"name":"1-aminocyclopropane-1-carboxylate deaminase activity","secondary_identifiers":["MetaCyc:4.1.99.4-RXN","EC:3.5.99.7","KEGG_REACTION:R00997","UM-BBD_reactionID:r0357","GO:0018806"],"synonyms":[{"name":"1-aminocyclopropane carboxylic acid deaminase activity","type":"related"},{"name":"1-aminocyclopropane-1-carboxylate aminohydrolase (isomerizing)","type":"related"},{"name":"1-aminocyclopropane-1-carboxylate endolyase (deaminating) activity","type":"related"},{"name":"ACC deaminase activity","type":"related"}],"termid":"GO:0008660"}


id: PATO:0001120
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001120 relative momentum value (obsolete PATO:0001120)","termid":"PATO:0001120"}


id: PBO:0078753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase 44 homolog","termid":"PBO:0078753"}


id: GO:0042470
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A tissue-specific, membrane-bounded cytoplasmic organelle within which melanin pigments are synthesized and stored. Melanosomes are synthesized in melanocyte cells.","definition_xrefs":["PMID:11584301","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pigment granule","termid":"GO:0048770"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"melanosome","secondary_identifiers":["Wikipedia:Melanosome"],"termid":"GO:0042470"}


id: MONDO:0011766
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46,XY complete gonadal dysgenesis","termid":"MONDO:0010765"},{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome","secondary_identifiers":["GARD:17034","MEDGEN:1727162","MESH:C567773","Orphanet:168563","UMLS:C5436061","OMIM:607080"],"synonyms":[{"name":"46,XY gonadal dysgenesis, partial, with MINIFASCICULAR neuropathy","type":"related"},{"name":"46XY gonadal dysgenesis with minifascicular neuropathy","type":"exact"}],"termid":"MONDO:0011766","xrefs":{"Monarch":{"xref_id":"0011766"}}}


id: PBO:0068403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 222","termid":"PBO:0068403"}


id: MONDO:0004755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection of ruminants with tapeworms of the genus Moniezia.","definition_xrefs":["MESH:D008989"],"direct_ancestors":[{"relation_name":"is_a","term_name":"helminthiasis","termid":"MONDO:0004664"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monieziasis","secondary_identifiers":["DOID:931","MEDGEN:6424","UMLS:C0026414"],"termid":"MONDO:0004755","xrefs":{"Monarch":{"xref_id":"0004755"}}}


id: PBO:0078952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon TCT) 3-2","termid":"PBO:0078952"}


id: MONDO:0042962
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":"alopecia","termid":"MONDO:0004907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Slti-Salem syndrome","secondary_identifiers":["UMLS:C2931284","MESH:C536673","MEDGEN:419036"],"synonyms":[{"name":"Slti Salem syndrome","type":"related"},{"name":"hypogonadism and frontoparietal alopecia","type":"related"},{"name":"hypogonadotropic hypogonadism alopecia","type":"related"}],"termid":"MONDO:0042962","xrefs":{"Monarch":{"xref_id":"0042962"}}}


id: PBO:0052226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel tetramerization domain containing 4","termid":"PBO:0052226"}


id: GO:0090287
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a growth factor stimulus.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to stimulus","termid":"GO:0048583"},{"relation_name":"regulates","term_name":"cellular response to growth factor stimulus","termid":"GO:0071363"}],"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 cellular response to growth factor stimulus","termid":"GO:0090287"}


id: MONDO:0016921
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal duplication","termid":"MONDO:0000762"},{"relation_name":"is_a","term_name":"chromosome 1 disorder","termid":"MONDO:0700008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial duplication of chromosome 1","secondary_identifiers":["Orphanet:262191","GARD:20842","SCTID:726338000","UMLS:C4518488","MEDGEN:1379629"],"synonyms":[{"name":"partial duplication of chromosome type 1","type":"exact"},{"name":"partial trisomy of chromosome 1","type":"exact"}],"termid":"MONDO:0016921","xrefs":{"Monarch":{"xref_id":"0016921"}}}


id: GO:0000402
data:
  {"annotated_genes":["SJAG_04752"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75615],"is_not":false,"summary":null,"term":"GO:0000402"}]},"cv_name":"molecular_function","definition":"Binding to a DNA segment containing the crossed form of a four-way junction, also known as a Holliday junction, a structure where two DNA double strands are held together by reciprocal exchange of two of the four strands, one strand each from the two original helices. The crossed form of a four-way junction cannot be diagrammed without any of the strands crossing over, and instead contains a single crossover between two of the strands.","definition_xrefs":["GOC:krc","PMID:15563464","ISBN:0815332181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"four-way junction DNA binding","termid":"GO:0000400"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04752":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003677","GO:0005488"],"is_obsolete":false,"name":"crossed form four-way junction DNA binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"crossed form Holliday junction binding","type":"exact"}],"termid":"GO:0000402","terms_by_termid":{"GO:0000402":null}}


id: MONDO:0011230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by benign depositions of calcium in the posterior longitudinal ligament. Signs and symptoms result from the compression of nerve roots and include motor and sensory disturbances in the lower and upper extremities, and pain in the neck and arms.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ossification of the posterior longitudinal ligament of the spine","secondary_identifiers":["OMIM:602475","SCTID:90448008","NCIT:C84975","UMLS:C1865343","DOID:0060887","EFO:0005895","MESH:C537143","NANDO:1200371","MEDGEN:355447"],"synonyms":[{"name":"OPLL","type":"exact"},{"name":"ossification of Posterior longitudinal ligament","type":"exact"},{"name":"ossification of the POSTERIOR longitudinal ligament of spine","type":"related"}],"termid":"MONDO:0011230","xrefs":{"Monarch":{"xref_id":"0011230"}}}


id: GO:0015491
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: cation A(out) + cation B(in) = cation A(in) + cation B(out).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cation:cation antiporter activity (obsolete GO:0015491)","termid":"GO:0015491"}


id: GO:0045592
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ovarian cumulus cell differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell differentiation","termid":"GO:0030856"},{"relation_name":"is_a","term_name":"regulation of antral ovarian follicle growth","termid":"GO:2000387"},{"relation_name":"regulates","term_name":"cumulus cell differentiation","termid":"GO:0001549"}],"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 cumulus cell differentiation","synonyms":[{"name":"regulation of ovarian cumulus cell differentiation","type":"exact"}],"termid":"GO:0045592"}


id: GO:1900243
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of synaptic vesicle endocytosis.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of endocytosis","termid":"GO:0045806"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle endocytosis","termid":"GO:1900242"},{"relation_name":"is_a","term_name":"negative regulation of synaptic vesicle recycling","termid":"GO:1903422"},{"relation_name":"negatively_regulates","term_name":"synaptic vesicle endocytosis","termid":"GO:0048488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"negative regulation of synaptic vesicle endocytosis","synonyms":[{"name":"down regulation of synaptic vesicle endocytosis","type":"exact"},{"name":"down regulation of synaptic vesicle retrieval","type":"related"},{"name":"down-regulation of synaptic vesicle endocytosis","type":"exact"},{"name":"down-regulation of synaptic vesicle retrieval","type":"related"},{"name":"downregulation of synaptic vesicle endocytosis","type":"exact"},{"name":"downregulation of synaptic vesicle retrieval","type":"related"},{"name":"inhibition of synaptic vesicle endocytosis","type":"narrow"},{"name":"inhibition of synaptic vesicle retrieval","type":"related"},{"name":"negative regulation of synaptic vesicle retrieval","type":"related"}],"termid":"GO:1900243"}


id: PR:Q9USM6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cytochrome b5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04489"],"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":"cytochrome b5 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16A11.10c","secondary_identifiers":["UniProtKB:Q9USM6"],"synonyms":[{"name":"Spom972h-CYB5A","type":"exact"}],"termid":"PR:Q9USM6"}


id: PBO:0038626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atypical chemokine receptor 2","termid":"PBO:0038626"}


id: PBO:0027246
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-polyadenylated_25S_rRNA_absent_from_cell","termid":"PBO:0027246"}


id: PBO:0067873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 175","termid":"PBO:0067873"}


id: PBO:0070093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 7 pseudogene","termid":"PBO:0070093"}


id: PBO:0036013
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_acetylation_during_vegetative_growth","termid":"PBO:0036013"}


id: PBO:0089203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GID complex subunit, Ran GTPase binding protein Gid1","termid":"PBO:0089203"}


id: PBO:0057468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 586","termid":"PBO:0057468"}


id: PBO:0078455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor gamma variable 7 (pseudogene)","termid":"PBO:0078455"}


id: PBO:0082278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Anthranilate synthase; catalyzes the initial step of tryptophan biosynthesis, forms multifunctional hetero-oligomeric anthranilate synthase:indole-3-glycerol phosphate synthase enzyme complex with Trp3p","termid":"PBO:0082278"}


id: GO:0097646
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by an extracellular member of the calcitonin family (e.g. adrenomedullin, adrenomedullin 2 (intermedin), amylin, calcitonin and calcitonin gene-related peptides (CGRPs)) binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process.","definition_xrefs":["PMID:12037140","PMID:18687416","GOC:bhm","PMID:10871296"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"}],"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":"calcitonin family receptor signaling pathway","synonyms":[{"name":"calcitonin family receptor signalling pathway","type":"exact"}],"termid":"GO:0097646"}


id: GO:0061128
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases 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 DIF-2. DIF-2 is a chlorinated alkylphenone.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of positive chemotaxis to cAMP by DIF-2","termid":"GO:0061121"},{"relation_name":"is_a","term_name":"positive regulation of positive chemotaxis to cAMP by chlorinated alkylphenone","termid":"GO:0061124"}],"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 chemotaxis to cAMP by DIF-2","termid":"GO:0061128"}


id: PBO:0034361
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-developmentally_induced_by","termid":"PBO:0034361"}


id: PBO:0082587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cis-golgi GTPase-activating protein (GAP) for yeast Rabs; the Rab family members are Ypt1p (in vivo) and for Ypt1p, Sec4p, Ypt7p, and Ypt51p (in vitro); involved in vesicle docking and fusion; interacts with autophagosome component Atg8p","termid":"PBO:0082587"}


id: GO:0048146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of multiplication or reproduction of fibroblast cells.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell population proliferation","termid":"GO:0008284"},{"relation_name":"is_a","term_name":"regulation of fibroblast proliferation","termid":"GO:0048145"},{"relation_name":"positively_regulates","term_name":"fibroblast proliferation","termid":"GO:0048144"}],"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 fibroblast proliferation","synonyms":[{"name":"activation of fibroblast proliferation","type":"narrow"},{"name":"stimulation of fibroblast proliferation","type":"narrow"},{"name":"up regulation of fibroblast proliferation","type":"exact"},{"name":"up-regulation of fibroblast proliferation","type":"exact"},{"name":"upregulation of fibroblast proliferation","type":"exact"}],"termid":"GO:0048146"}


id: PBO:0043072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor nicotinic alpha 1 subunit","termid":"PBO:0043072"}


id: PBO:0114106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane sulfate transmembrane transporter Vsb1","termid":"PBO:0114106"}


id: PBO:0086016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; SWAT-GFP, seamless-GFP and mCherry fusion proteins localize to cytosol; conserved among Saccharomyces sensu stricto species","termid":"PBO:0086016"}


id: GO:0050906
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events involved in sensory perception in which a sensory stimulus is received and converted into a molecular signal.","definition_xrefs":["GOC:dos","GOC:ai","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of stimulus","termid":"GO:0051606"},{"relation_name":"part_of","term_name":"sensory perception","termid":"GO:0007600"}],"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","secondary_identifiers":["Wikipedia:Transduction_(physiology)"],"synonyms":[{"name":"sensory detection of stimulus","type":"exact"},{"name":"sensory perception, sensory transduction of stimulus","type":"exact"},{"name":"sensory perception, stimulus detection","type":"exact"},{"name":"sensory transduction","type":"exact"}],"termid":"GO:0050906"}


id: PBO:0002508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoplasmic cysteine-tRNA ligase Crs1 (predicted)","termid":"PBO:0002508"}


id: MONDO:0032865
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary fibrosis and/or bone marrow failure, telomere-related","termid":"MONDO:0000148"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0019303"],"is_obsolete":false,"name":"pulmonary fibrosis and/or bone marrow failure, telomere-related, 5","secondary_identifiers":["UMLS:C5231457","MEDGEN:1684878","OMIM:618674"],"synonyms":[{"name":"PFBMFT5","type":"related"},{"name":"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 5","type":"related"},{"name":"ZCCHC8-related telomere biology disorder","type":"exact"}],"termid":"MONDO:0032865","xrefs":{"Monarch":{"xref_id":"0032865"}}}


id: GO:0032047
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A double-membrane-bounded organelle that functions in iron-sulfur protein maturation; evolutionarily derived from mitochondria. The mitosome has been detected only in anaerobic or microaerophilic organisms that do not have mitochondria, such as Entamoeba histolytica, Giardia intestinalis and several species of Microsporidia. These organisms are not capable of gaining energy from oxidative phosphorylation, which is normally performed by mitochondria.","definition_xrefs":["PMID:10361303","GOC:giardia","PMID:14614504","PMID:24316280"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membrane-bounded organelle","termid":"GO:0043231"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"mitosome","secondary_identifiers":["Wikipedia:Mitosome"],"synonyms":[{"name":"crypton","type":"exact"}],"termid":"GO:0032047"}


id: PBO:0011128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar amino acid import transporter Avt5","termid":"PBO:0011128"}


id: PBO:0064722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 58","termid":"PBO:0064722"}


id: PBO:0027587
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_sister_chromatid_cohesion_along_chromosome_arms","termid":"PBO:0027587"}


id: PBO:0082116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Acetyl-coA synthetase isoform; along with Acs2p, acetyl-coA synthetase isoform is the nuclear source of acetyl-coA for histone acetylation; expressed during growth on nonfermentable carbon sources and under aerobic conditions","termid":"PBO:0082116"}


id: GO:0043101
data:
  {"annotated_genes":["SJAG_01500","SJAG_06634","SJAG_03881","SJAG_00134","SJAG_03298","SJAG_01859","SJAG_01070","SJAG_04123","SJAG_03096"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006168"},{"annotations":[117167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006169"},{"annotations":[57088,74276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044209"},{"annotations":[75974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"},{"annotations":[65066,75975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032264"},{"annotations":[70152],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006190"},{"annotations":[80259,99664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034355"},{"annotations":[66865,61946,94081,73829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006166"},{"annotations":[75976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"Any process that generates a purine-containing compound, any nucleobase, nucleoside, nucleotide or nucleic acid that contains a purine base, from derivatives of them without de novo synthesis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic compound salvage","termid":"GO:0043094"},{"relation_name":"is_a","term_name":"purine-containing compound biosynthetic process","termid":"GO:0072522"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00134":null,"SJAG_01070":null,"SJAG_01500":null,"SJAG_01859":null,"SJAG_03096":null,"SJAG_03298":null,"SJAG_03881":null,"SJAG_04123":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"purine-containing compound salvage","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-74217"],"synonyms":[{"name":"purine salvage","type":"related"}],"termid":"GO:0043101","terms_by_termid":{"GO:0006166":null,"GO:0006168":null,"GO:0006169":null,"GO:0006190":null,"GO:0032263":null,"GO:0032264":null,"GO:0032265":null,"GO:0034355":null,"GO:0044209":null}}


id: PBO:0054790
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 2203","termid":"PBO:0054790"}


id: PBO:0013085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Prp16","termid":"PBO:0013085"}


id: GO:0019113
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of a monooxygenase reaction in which oxygen is incorporated into limonene.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"limonene monooxygenase activity","termid":"GO:0019113"}


id: GO:0052109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates, maintains or increases the frequency, rate or extent of the deposition of callose by the host in its cell walls, occurring as part of the defense response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by symbiont of defense-related host cell wall callose deposition (obsolete GO:0052109)","synonyms":[{"name":"activation by symbiont of defense-related host cell wall callose deposition","type":"exact"},{"name":"positive regulation by organism of defense-related callose deposition in other organism involved in symbiotic interaction","type":"broad"},{"name":"positive regulation by organism of defense-related cell wall callose deposition in other organism involved in symbiotic interaction","type":"broad"},{"name":"positive regulation by symbiont of defense-related host callose deposition","type":"related"},{"name":"positive regulation by symbiont of defense-related host cell wall callose deposition","type":"related"},{"name":"stimulation by symbiont of defense-related host cell wall callose deposition","type":"related"},{"name":"up regulation by symbiont of defense-related host cell wall callose deposition","type":"related"},{"name":"up-regulation by symbiont of defense-related host cell wall callose deposition","type":"related"},{"name":"upregulation by symbiont of defense-related host cell wall callose deposition","type":"related"}],"termid":"GO:0052109"}


id: GO:0051135
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of natural killer T cell activation.","definition_xrefs":["PMID:9133426","ISBN:0781735149","PMID:12154375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of alpha-beta T cell activation","termid":"GO:0046635"},{"relation_name":"is_a","term_name":"regulation of NK T cell activation","termid":"GO:0051133"},{"relation_name":"positively_regulates","term_name":"NK T cell activation","termid":"GO:0051132"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"positively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"positive regulation of NK T cell activation","synonyms":[{"name":"activation of NK T cell activation","type":"narrow"},{"name":"positive regulation of NK T lymphocyte activation","type":"exact"},{"name":"positive regulation of NK T-cell activation","type":"exact"},{"name":"positive regulation of NK T-lymphocyte activation","type":"exact"},{"name":"positive regulation of NKT cell activation","type":"exact"},{"name":"positive regulation of NT cell activation","type":"exact"},{"name":"positive regulation of natural T cell activation","type":"exact"},{"name":"positive regulation of natural killer T cell activation","type":"exact"},{"name":"stimulation of NK T cell activation","type":"narrow"},{"name":"up regulation of NK T cell activation","type":"exact"},{"name":"up-regulation of NK T cell activation","type":"exact"},{"name":"upregulation of NK T cell activation","type":"exact"}],"termid":"GO:0051135"}


id: PATO:0000608
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphological quality inhering in a bearer by virtue of the bearer's affording blocked passage or view.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"closure","termid":"PATO:0000136"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"closed","synonyms":[{"name":"blocked","type":"related"}],"termid":"PATO:0000608"}


id: PBO:0059593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ATP6 pseudogene 5","termid":"PBO:0059593"}


id: GO:0005391
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + Na+(in) + K+(out) = ADP + phosphate + Na+(out) + K+(in).","definition_xrefs":["EC:7.2.2.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"P-type sodium transporter activity","termid":"GO:0008554"},{"relation_name":"is_a","term_name":"P-type potassium transmembrane transporter activity","termid":"GO:0008556"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"P-type sodium:potassium-exchanging transporter activity","secondary_identifiers":["MetaCyc:3.6.3.9-RXN","TC:3.A.3.1.1","RHEA:18353","Wikipedia:ATPase\\,_Na%2B/K%2B_transporting\\,_alpha_1","Reactome:R-HSA-936897"],"synonyms":[{"name":"Na(+)/K(+)-ATPase activity","type":"related"},{"name":"Na(+)/K(+)-exchanging ATPase activity","type":"related"},{"name":"Na+,K+-ATPase activity","type":"related"},{"name":"Na+/K+-ATPase activity","type":"related"},{"name":"Na+/K+-exchanging ATPase activity","type":"related"},{"name":"Na,K-activated ATPase activity","type":"related"},{"name":"P-type sodium:potassium-exchanging ATPase activity","type":"exact"},{"name":"sodium pump","type":"broad"},{"name":"sodium/potassium-exchanging ATPase activity","type":"exact"},{"name":"sodium/potassium-transporting ATPase activity","type":"exact"},{"name":"sodium:potassium exchanging ATPase activity","type":"exact"},{"name":"sodium:potassium-exchanging ATPase activity","type":"exact"}],"termid":"GO:0005391"}


id: GO:1900202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of spread of virus in host, cell to cell.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of spread of virus in host, cell to cell (obsolete GO:1900202)","synonyms":[{"name":"down regulation of cell to cell spread of virus within host","type":"exact"},{"name":"down regulation of spread of virus in host, cell to cell","type":"exact"},{"name":"down regulation of spread of virus within host, cell to cell","type":"exact"},{"name":"down regulation of viral spread within host, cell to cell","type":"exact"},{"name":"down-regulation of cell to cell spread of virus within host","type":"exact"},{"name":"down-regulation of spread of virus in host, cell to cell","type":"exact"},{"name":"down-regulation of spread of virus within host, cell to cell","type":"exact"},{"name":"down-regulation of viral spread within host, cell to cell","type":"exact"},{"name":"downregulation of cell to cell spread of virus within host","type":"exact"},{"name":"downregulation of spread of virus in host, cell to cell","type":"exact"},{"name":"downregulation of spread of virus within host, cell to cell","type":"exact"},{"name":"downregulation of viral spread within host, cell to cell","type":"exact"},{"name":"inhibition of cell to cell spread of virus within host","type":"exact"},{"name":"inhibition of spread of virus in host, cell to cell","type":"narrow"},{"name":"inhibition of spread of virus within host, cell to cell","type":"exact"},{"name":"inhibition of viral spread within host, cell to cell","type":"exact"},{"name":"negative regulation of cell to cell spread of virus within host","type":"exact"},{"name":"negative regulation of spread of virus in host, cell to cell","type":"exact"},{"name":"negative regulation of spread of virus within host, cell to cell","type":"exact"},{"name":"negative regulation of viral spread within host, cell to cell","type":"exact"}],"termid":"GO:1900202"}


id: PBO:0089009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid elongase Elo2","termid":"PBO:0089009"}


id: PBO:0045940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ephrin A5","termid":"PBO:0045940"}


id: MONDO:0032910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, nuclear type","termid":"MONDO:0100223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex 1 deficiency, nuclear type 34","secondary_identifiers":["OMIM:618776","DOID:0112091","GARD:16378","MEDGEN:1720533","UMLS:C5394053"],"synonyms":[{"name":"MC1DN34","type":"related"},{"name":"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 34","type":"related"}],"termid":"MONDO:0032910","xrefs":{"Monarch":{"xref_id":"0032910"}}}


id: MOD:00739
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes a cluster of iron and sulfur atoms for hydrogen atoms.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron containing modified residue","termid":"MOD:00738"},{"relation_name":"is_a","term_name":"sulfur containing modified residue","termid":"MOD:00860"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster containing modification","synonyms":[{"name":"FeSRes","type":"exact"}],"termid":"MOD:00739"}


id: PBO:0072183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S16 pseudogene 10","termid":"PBO:0072183"}


id: PBO:0083722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESCRT-I subunit required to stabilize ESCRT-I core complex oligomers; the ESCRT-I core complex (Stp22p, Vps28p, Srn2p) is involved in ubiquitin-dependent sorting of proteins into the endosome; deletion mutant is sensitive to rapamycin and nystatin","termid":"PBO:0083722"}


id: MONDO:0850618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anthrax disease that is characterized by infection at the injection site or deep under the skin or in the muscle where the drug was injected and is caused by heroin contaminated with anthrax spores.","definition_xrefs":["DOID:0081239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anthrax infection","termid":"MONDO:0005119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"injection anthrax","termid":"MONDO:0850618","xrefs":{"Monarch":{"xref_id":"0850618"}}}


id: PBO:0060579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBPF member 15","termid":"PBO:0060579"}


id: PBO:0063832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"putative homeodomain transcription factor 2","termid":"PBO:0063832"}


id: MONDO:0001360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ocular hypotension","termid":"MONDO:0004390"}],"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":"blind hypotensive eye","secondary_identifiers":["MEDGEN:509659","SCTID:23360000","UMLS:C0154788","DOID:11766","ICD9:360.41"],"termid":"MONDO:0001360","xrefs":{"Monarch":{"xref_id":"0001360"}}}


id: GO:0090690
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A receptor complex that consists of two or more different receptor complexes that individually undergo combination with a hormone, neurotransmitter, drug or intracellular messenger. The formation of the higher level complex initiates a change in cell function.","definition_xrefs":["GOC:PARL","PMID:24157794","PMID:22035699","GOC:pad"],"gene_count":0,"genotype_count":0,"name":"obsolete heteroreceptor complex (obsolete GO:0090690)","termid":"GO:0090690"}


id: PBO:0070518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L6 pseudogene 17","termid":"PBO:0070518"}


