# terms

id: GO:0001576
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a glycosphingolipid with a core structure of GalNAc-beta-(1->3)-Gal-alpha-(1->4)-Glc(I).","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"globoside metabolic process","termid":"GO:0001575"},{"relation_name":"is_a","term_name":"glycosphingolipid biosynthetic process","termid":"GO:0006688"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"globoside biosynthetic process","synonyms":[{"name":"globoside anabolism","type":"exact"},{"name":"globoside biosynthesis","type":"exact"},{"name":"globoside formation","type":"exact"},{"name":"globoside synthesis","type":"exact"}],"termid":"GO:0001576"}


id: FYPO:0002190
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, is shaped in the form of a spheroid, and has a larger volume than normal. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"swollen spheroid vegetative cell","termid":"FYPO:0000945"},{"relation_name":"is_a","term_name":"inviable swollen vegetative cell with abnormal cell shape","termid":"FYPO:0002415"},{"relation_name":"is_a","term_name":"inviable spheroid vegetative cell","termid":"FYPO:0002482"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000005","FYPO:0000004","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"inviable swollen spheroid vegetative cell","synonyms":[{"name":"inviable enlarged spheroid vegetative cell","type":"related"},{"name":"inviable enlarged volume spheroid vegetative cell","type":"exact"},{"name":"inviable large spheroid vegetative cell","type":"related"},{"name":"inviable swollen rounded vegetative cell","type":"exact"},{"name":"inviable swollen spheroid cell during vegetative growth","type":"exact"},{"name":"inviable swollen spheroid vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable, increased spheroid vegetative cell size","type":"related"},{"name":"inviable, increased spheroid vegetative cell volume","type":"exact"},{"name":"lethal; swollen spheroid vegetative cell","type":"exact"}],"termid":"FYPO:0002190"}


id: PBO:0041813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coactivator associated arginine methyltransferase 1 pseudogene 1","termid":"PBO:0041813"}


id: MONDO:0971058
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare bacterial infectious disease characterized by development of endothelial cell-derived, blood-filled tumors on the surface of the skin during the chronic phase of infection with Bartonella bacilliformis. The lesions can persist for months to years and may cause pain and scarring due to ulceration. They are classified as miliary (multiple red papules of <3 mm in diameter), mular (blood-filled nodules), and diffuse (groups of subdermal nodules >5 mm in diameter). Eruptions may be accompanied by fever and malaise, lymphadenopathy, acute bone and joint pains, and headache. Fatality rates during this phase are low.","definition_xrefs":["Orphanet:659759"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Oroya fever","termid":"MONDO:0018984"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"verruga peruana","secondary_identifiers":["UMLS:C0042552","MEDGEN:21848"],"termid":"MONDO:0971058","xrefs":{"Monarch":{"xref_id":"0971058"}}}


id: PBO:0026978
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_phosphatidylinositol-3-phosphate_binding","termid":"PBO:0026978"}


id: PBO:0017904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NST UDP-N-acetylglucosamine transmembrane transporter (predicted)","termid":"PBO:0017904"}


id: PBO:0036276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mouse transcriptional regulator HCNGP-like (predicted)","termid":"PBO:0036276"}


id: FYPO:0006038
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A metabolism phenotype observed in the vegetative growth phase of the life cycle in which the initiation of translation in the cytoplasm is normal (i.e. indistinguishable from wild type). Translational initiation is he process preceding formation of the peptide bond between the first two amino acids of a protein in the cytoplasm.","definition_xrefs":["GO:0002183","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation phenotype","termid":"FYPO:0000291"},{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal cytoplasmic translational initiation","synonyms":[{"name":"normal cytoplasmic translation initiation","type":"exact"},{"name":"normal cytoplasmic translational initiation during mitotic cell cycle","type":"related"},{"name":"normal cytoplasmic translational initiation during vegetative growth","type":"exact"}],"termid":"FYPO:0006038"}


id: PBO:0057090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 186","termid":"PBO:0057090"}


id: PBO:0050401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein C pseudogene 2","termid":"PBO:0050401"}


id: MONDO:0017277
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"},{"relation_name":"is_a","term_name":"chromosome 12 disorder","termid":"MONDO:0700019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of chromosome 12","secondary_identifiers":["GARD:21115","MEDGEN:1826080","UMLS:C5680422","Orphanet:282124"],"synonyms":[{"name":"partial deletion of chromosome type 12","type":"exact"},{"name":"partial monosomy of chromosome 12","type":"exact"}],"termid":"MONDO:0017277","xrefs":{"Monarch":{"xref_id":"0017277"}}}


id: PR:Q9Y719
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mok13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y719"],"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":"cell wall alpha-1,3-glucan synthase mok13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16D10.05","synonyms":[{"name":"Spom972h-mok13","type":"exact"}],"termid":"PR:Q9Y719"}


id: GO:0052021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The alteration by an organism of the levels of ethylene in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by symbiont of ethylene levels in host (obsolete GO:0052021)","synonyms":[{"name":"modulation by organism of ethylene levels in other organism involved in symbiotic interaction","type":"broad"}],"termid":"GO:0052021"}


id: GO:2000795
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of epithelial cell proliferation involved in lung morphogenesis.","definition_xrefs":["PMID:21513708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell proliferation","termid":"GO:0050680"},{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation involved in lung morphogenesis","termid":"GO:2000794"},{"relation_name":"negatively_regulates","term_name":"epithelial cell proliferation involved in lung morphogenesis","termid":"GO:0060502"}],"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 epithelial cell proliferation involved in lung morphogenesis","termid":"GO:2000795"}


id: PBO:0044052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine and glycine rich protein 3","termid":"PBO:0044052"}


id: MONDO:0019815
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Accessory tricuspid valve tissue is a rare, congenital, atrioventricular valve malformation characterized by fixed or mobile accessory tissue on the tricuspid valve, usually associated with other complex congenital heart anomalies (atrial septal defect, ventricular septal defect, transposition of great arteries, tetralogy Fallot). It may present clinically with systolic murmur, dyspnea, cyanosis, depending also on accompanying congenital heart anomaly.","definition_xrefs":["Orphanet:95462"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital tricuspid malformation","termid":"MONDO:0020289"}],"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":"accessory tricuspid valve tissue","secondary_identifiers":["GARD:19264","UMLS:C5566613","MEDGEN:1798036"],"termid":"MONDO:0019815","xrefs":{"Monarch":{"xref_id":"0019815"}}}


id: GO:0019548
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of arginine into other compounds, including spermine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arginine metabolic process","termid":"GO:0006525"},{"relation_name":"is_a","term_name":"spermine metabolic process","termid":"GO:0008215"},{"relation_name":"is_a","term_name":"alpha-amino acid catabolic process","termid":"GO:1901606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"arginine catabolic process to spermine","secondary_identifiers":["MetaCyc:ARGSPECAT-PWY"],"synonyms":[{"name":"arginine breakdown to spermine","type":"exact"},{"name":"arginine degradation to spermine","type":"exact"}],"termid":"GO:0019548"}


id: PBO:0109829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TTT co-chaperone complex, WD repeat subunit Asa1","termid":"PBO:0109829"}


id: GO:0034978
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the homeodomain proteins PDX1, PBX1b and MRG1 (MEIS2) and is involved in the transcriptional regulation of pancreatic acinar cell-specific genes.","definition_xrefs":["PMID:9710595","PMID:11279116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"PDX1-PBX1b-MRG1 complex","synonyms":[{"name":"acinar cell-specific C complex","type":"exact"}],"termid":"GO:0034978"}


id: MONDO:0008727
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency is a very rare form of congenital adrenal hyperplasia (CAH) encompassing salt-wasting and non-salt wasting forms with a wide variety of symptoms, including glucocorticoid deficiency and male undervirilization manifesting as a micropenis to severe perineoscrotal hypospadias.","definition_xrefs":["Orphanet:90791"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"},{"relation_name":"is_a","term_name":"congenital adrenal hyperplasia","termid":"MONDO:0018479"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency","secondary_identifiers":["MESH:C538236","NANDO:1200398","OMIM:201810","SCTID:54470008","NCIT:C131088","NANDO:2200371","GARD:9152","icd11.foundation:929626064","UMLS:C0342471","MEDGEN:452446"],"synonyms":[{"name":"3-BETA-hydroxysteroid dehydrogenase, type II, deficiency OF","type":"related"},{"name":"3-Beta-HSD deficiency","type":"related"},{"name":"3-Beta-hydroxysteroid dehydrogenase deficiency","type":"related"},{"name":"3-beta HSD deficiency","type":"exact"},{"name":"3b-hydroxysteroid dehydrogenase deficiency","type":"related"},{"name":"CAH due to 3-beta-hydroxysteroid dehydrogenase deficiency","type":"exact"},{"name":"HSD3B deficiency","type":"related"},{"name":"adrenal hyperplasia 2","type":"related"},{"name":"adrenal hyperplasia II","type":"related"},{"name":"adrenal hyperplasia, congenital, due to 3-BETA-hydroxysteroid dehydrogenase 2 deficiency","type":"related"},{"name":"adrenal hyperplasia, congenital, due to 3-Beta-hydroxysteroid dehydrogenase 2 deficiency","type":"related"},{"name":"type II 3-beta-hydroxysteroid dehydrogenase deficiency","type":"related"}],"termid":"MONDO:0008727","xrefs":{"Monarch":{"xref_id":"0008727"}}}


id: MONDO:0958076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare form of spina bifida/open neural tube defect (NTD) chacterized by absence of a cystic component, dysplastic meninges and neural placode exposed through a defect in the posterior vertebral arches (spina bifida) that are contiguous with surrounding skin. The placode is at or below the skin plane and is typically associated with a Chiari II malformation. It is usually isolated or rarely associated with split cord malformation.","definition_xrefs":["Orphanet:645398"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spina bifida aperta","termid":"MONDO:0017062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"myeloschisis","secondary_identifiers":["MEDGEN:539965","UMLS:C0266507","icd11.foundation:1547705800"],"termid":"MONDO:0958076","xrefs":{"Monarch":{"xref_id":"0958076"}}}


id: PBO:0040392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V1 subunit E1","termid":"PBO:0040392"}


id: PATO:0001628
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A wholeness quality inhering in a bearer by virtue of the bearer's lacks enough functionality.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sufficiency","termid":"PATO:0001626"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insufficient","synonyms":[{"name":"inadequate ","type":"related"}],"termid":"PATO:0001628"}


id: PBO:0085433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Polyamine transporter of the major facilitator superfamily; member of the 12-spanner drug:H(+) antiporter DHA1 family; specific for spermine; localizes to the plasma membrane; TPO3 has a paralog, TPO2, that arose from the whole genome duplication","termid":"PBO:0085433"}


id: GO:0005774
data:
  {"annotated_genes":["SJAG_02414","SJAG_04506","SJAG_02578","SJAG_02565","SJAG_02782","SJAG_00136","SJAG_03848","SJAG_00877","SJAG_04643","SJAG_05294","SJAG_03450","SJAG_01036","SJAG_01571","SJAG_01324","SJAG_04028","SJAG_02356","SJAG_03725","SJAG_01080","SJAG_00534","SJAG_00821","SJAG_02433","SJAG_03138","SJAG_03447","SJAG_07012","SJAG_02117","SJAG_03406","SJAG_02103","SJAG_02603","SJAG_03442","SJAG_03497","SJAG_04910","SJAG_03785","SJAG_03895","SJAG_01319","SJAG_01145","SJAG_05210","SJAG_03511","SJAG_03960","SJAG_01236","SJAG_01795","SJAG_01509","SJAG_03656","SJAG_03355","SJAG_00824","SJAG_04502","SJAG_00029","SJAG_03100","SJAG_03250","SJAG_03405","SJAG_00732","SJAG_02231","SJAG_01400","SJAG_03005","SJAG_02424","SJAG_04963","SJAG_00457","SJAG_01027","SJAG_01991","SJAG_00688","SJAG_01913","SJAG_02344","SJAG_02853","SJAG_03089","SJAG_04966","SJAG_00638","SJAG_01299","SJAG_02023","SJAG_03899","SJAG_02289","SJAG_02665","SJAG_01983","SJAG_01619","SJAG_00570","SJAG_03009","SJAG_01817","SJAG_01505","SJAG_02029","SJAG_00380","SJAG_01447","SJAG_01397","SJAG_03401","SJAG_01112","SJAG_00299","SJAG_04471","SJAG_03962","SJAG_06309","SJAG_03909","SJAG_02656","SJAG_05194","SJAG_04616","SJAG_02902","SJAG_04496","SJAG_04698","SJAG_04725","SJAG_03072","SJAG_03360","SJAG_02723","SJAG_01032","SJAG_01941","SJAG_01078","SJAG_01471","SJAG_00212","SJAG_03137","SJAG_01598","SJAG_01990","SJAG_04975","SJAG_00051","SJAG_04867","SJAG_04955","SJAG_05184","SJAG_00516","SJAG_03403","SJAG_01772","SJAG_00204","SJAG_02765","SJAG_03371","SJAG_04232","SJAG_02699","SJAG_01783","SJAG_04023","SJAG_05213","SJAG_01320","SJAG_00771","SJAG_03667","SJAG_03256","SJAG_00561","SJAG_03928","SJAG_03400","SJAG_02716","SJAG_00209","SJAG_01344","SJAG_03987","SJAG_01184","SJAG_04015","SJAG_01803"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[68805,72630,75152,75286,77132,80173,90124,91233,108480,111649,112807,114717,121229],"is_not":false,"summary":null,"term":"GO:0005774"},{"annotations":[72262,73820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000421"},{"annotations":[118884,95838,76227,97463,97797,89830,98231,74378,74602,106802,71856,107538,109231,77047,95519,96404,75820,110117,73903,102046,109682,111133,78252,74268,106958,90880,105404,103785,111219,101794,74782,115089,71021,89848,95578,97839,99163,90963,90901,72261,92204,99433,93311,115273,101761,78180,90949,99853,82017,109024,111714,73664,74484,89544,115413,116201,95337,118480,119410,119669,80206,112241,106731,76722,74563,97914,100636,100676,97713,101384,103445,100507,108512,110518,95862,118408,119244,95704,120069,81605,97952,81455,95577,94706,97578,80346,81852,108505,76596,116194,116734,112103,72632,96435,81506,72134,100362,75134,105610,119469,80876,81791,94790,104830,119118,108980,93866,105726,72435,113638,118053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000329"},{"annotations":[81854,111834,115415,89545],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070772"},{"annotations":[109683,106960,95863,94707],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071986"},{"annotations":[72899,81547,81807,72973,76858,78930,96124,106463],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902500"},{"annotations":[91972,62725,93867,101762,97645,105727,97464],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000220"},{"annotations":[120605,72954,61085,111716,98424,104490,89849,100728],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000221"}]},"cv_name":"cellular_component","definition":"The lipid bilayer surrounding the vacuole and separating its contents from the cytoplasm of the cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bounding membrane of organelle","termid":"GO:0098588"},{"relation_name":"part_of","term_name":"vacuole","termid":"GO:0005773"}],"gene_count":135,"genes_by_uniquename":{"SJAG_00029":null,"SJAG_00051":null,"SJAG_00136":null,"SJAG_00204":null,"SJAG_00209":null,"SJAG_00212":null,"SJAG_00299":null,"SJAG_00380":null,"SJAG_00457":null,"SJAG_00516":null,"SJAG_00534":null,"SJAG_00561":null,"SJAG_00570":null,"SJAG_00638":null,"SJAG_00688":null,"SJAG_00732":null,"SJAG_00771":null,"SJAG_00821":null,"SJAG_00824":null,"SJAG_00877":null,"SJAG_01027":null,"SJAG_01032":null,"SJAG_01036":null,"SJAG_01078":null,"SJAG_01080":null,"SJAG_01112":null,"SJAG_01145":null,"SJAG_01184":null,"SJAG_01236":null,"SJAG_01299":null,"SJAG_01319":null,"SJAG_01320":null,"SJAG_01324":null,"SJAG_01344":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01505":null,"SJAG_01509":null,"SJAG_01571":null,"SJAG_01598":null,"SJAG_01619":null,"SJAG_01772":null,"SJAG_01783":null,"SJAG_01795":null,"SJAG_01803":null,"SJAG_01817":null,"SJAG_01913":null,"SJAG_01941":null,"SJAG_01983":null,"SJAG_01990":null,"SJAG_01991":null,"SJAG_02023":null,"SJAG_02029":null,"SJAG_02103":null,"SJAG_02117":null,"SJAG_02231":null,"SJAG_02289":null,"SJAG_02344":null,"SJAG_02356":null,"SJAG_02414":null,"SJAG_02424":null,"SJAG_02433":null,"SJAG_02565":null,"SJAG_02578":null,"SJAG_02603":null,"SJAG_02656":null,"SJAG_02665":null,"SJAG_02699":null,"SJAG_02716":null,"SJAG_02723":null,"SJAG_02765":null,"SJAG_02782":null,"SJAG_02853":null,"SJAG_02902":null,"SJAG_03005":null,"SJAG_03009":null,"SJAG_03072":null,"SJAG_03089":null,"SJAG_03100":null,"SJAG_03137":null,"SJAG_03138":null,"SJAG_03250":null,"SJAG_03256":null,"SJAG_03355":null,"SJAG_03360":null,"SJAG_03371":null,"SJAG_03400":null,"SJAG_03401":null,"SJAG_03403":null,"SJAG_03405":null,"SJAG_03406":null,"SJAG_03442":null,"SJAG_03447":null,"SJAG_03450":null,"SJAG_03497":null,"SJAG_03511":null,"SJAG_03656":null,"SJAG_03667":null,"SJAG_03725":null,"SJAG_03785":null,"SJAG_03848":null,"SJAG_03895":null,"SJAG_03899":null,"SJAG_03909":null,"SJAG_03928":null,"SJAG_03960":null,"SJAG_03962":null,"SJAG_03987":null,"SJAG_04015":null,"SJAG_04023":null,"SJAG_04028":null,"SJAG_04232":null,"SJAG_04471":null,"SJAG_04496":null,"SJAG_04502":null,"SJAG_04506":null,"SJAG_04616":null,"SJAG_04643":null,"SJAG_04698":null,"SJAG_04725":null,"SJAG_04867":null,"SJAG_04910":null,"SJAG_04955":null,"SJAG_04963":null,"SJAG_04966":null,"SJAG_04975":null,"SJAG_05184":null,"SJAG_05194":null,"SJAG_05210":null,"SJAG_05213":null,"SJAG_05294":null,"SJAG_06309":null,"SJAG_07012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005773","GO:0005575"],"is_obsolete":false,"name":"vacuolar membrane","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:40195311":null},"termid":"GO:0005774","terms_by_termid":{"GO:0000220":null,"GO:0000221":null,"GO:0000329":null,"GO:0000421":null,"GO:0005774":null,"GO:0070772":null,"GO:0071986":null,"GO:1902500":null}}


id: GO:0007298
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a border cell through the nurse cells to reach the oocyte. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mtg_sensu","PMID:10822261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"follicle cell of egg chamber migration","termid":"GO:0007297"}],"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":"border follicle cell migration","synonyms":[{"name":"border cell migration","type":"broad"}],"termid":"GO:0007298"}


id: FYPO:0002668
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of peptide-serine-N-acetyltransferase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal peptide alpha-N-acetyltransferase activity","termid":"FYPO:0007838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257","FYPO:0000654"],"is_obsolete":false,"name":"normal peptide-serine-N-acetyltransferase activity","termid":"FYPO:0002668"}


id: GO:1900473
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of phosphatidylcholine biosynthetic process by stopping, preventing, or reducing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:dgf","PMID:8056324","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of phosphatidylcholine biosynthetic process by negative regulation of transcription from RNA polymerase II promoter (obsolete GO:1900473)","synonyms":[{"name":"negative regulation of phosphatidylcholine anabolism by negative regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"negative regulation of phosphatidylcholine biosynthesis by negative regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"negative regulation of phosphatidylcholine formation by negative regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"negative regulation of phosphatidylcholine synthesis by negative regulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:1900473"}


id: MONDO:0010668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Skeletal dysplasia-intellectual disability syndrome combines skeletal anomalies (short stature, ridging of the metopic suture, fusion of cervical vertebrae, thoracic hemivertebrae, scoliosis, sacral hypoplasia and short middle phalanges) and mild intellectual deficit. It has been described in four male cousins in three sibships. Glucose intolerance was present in three cases, and imperforated anus in one case. Carrier females had minor manifestations (fusion of cervical vertebrae and glucose intolerance). Transmission seems to be X-linked.","definition_xrefs":["Orphanet:1436"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"spondylodysplastic dysplasia","termid":"MONDO:0019694"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"skeletal dysplasia-intellectual disability syndrome","secondary_identifiers":["GARD:3520","MESH:C564101","OMIM:309620","SCTID:722478008","UMLS:C1839729","MEDGEN:326949"],"synonyms":[{"name":"Christian syndrome","type":"exact"},{"name":"MRSD","type":"related"},{"name":"X-linked skeletal dysplasia-intellectual disability syndrome","type":"related"},{"name":"intellectual disability skeletal dysplasia abducens palsy","type":"related"},{"name":"intellectual disability, skeletal dysplasia, and abducens palsy","type":"related"},{"name":"mental retardation skeletal dysplasia abducens palsy","type":"related"},{"name":"mental retardation, skeletal dysplasia, and abducens palsy","type":"related"},{"name":"mental retardation-skeletal dysplasia","type":"exact"}],"termid":"MONDO:0010668","xrefs":{"Monarch":{"xref_id":"0010668"}}}


id: PBO:0029614
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_stubby_vegetative_cell","termid":"PBO:0029614"}


id: GO:0102640
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: paspalicine + O2 + NADPH + H+ = paspalinine + NADP + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete paspalinine synthase activity (obsolete GO:0102640)","termid":"GO:0102640"}


id: PBO:0003820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CUE domain protein","termid":"PBO:0003820"}


id: PBO:0080204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vezatin, adherens junctions transmembrane protein","termid":"PBO:0080204"}


id: GO:0005018
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with platelet-derived growth factor isoform PDGF-AA, PDGF-BB or PDGF-AB to initiate a change in cell activity.","definition_xrefs":["PMID:1657917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"platelet-derived growth factor receptor activity","termid":"GO:0005017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0016301","GO:0003674","GO:0016740","GO:0004672","GO:0003824","GO:0038023"],"is_obsolete":false,"name":"platelet-derived growth factor alpha-receptor activity","synonyms":[{"name":"PDGF alpha-receptor activity","type":"exact"},{"name":"alphaPDGF receptor activity","type":"exact"}],"termid":"GO:0005018"}


id: PBO:0049799
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex P5","termid":"PBO:0049799"}


id: MONDO:0005865
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extrinsic allergic alveolitis involving inflammation of the alveoli within the lung caused by hypersensitivity to the inhalation of organic dust particles derived from either the mushrooms, their spores or the compost in which the mushrooms are grown. It is usually caused by the spores of thermophilic actinomycetes.","definition_xrefs":["DOID:2708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypersensitivity pneumonitis","termid":"MONDO:0017853"}],"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":"mushroom workers' lung","secondary_identifiers":["UMLS:C0155889","SCTID:52333004","MEDGEN:102344","ICD9:495.5"],"synonyms":[{"name":"bunashimeji worker's lung","type":"narrow"},{"name":"mushroom workers lung","type":"exact"},{"name":"pholiota worker's lung","type":"narrow"},{"name":"pleurotus worker's lung","type":"narrow"},{"name":"shiitaki worker's lung","type":"narrow"},{"name":"shimeji worker's lung","type":"narrow"}],"termid":"MONDO:0005865","xrefs":{"Monarch":{"xref_id":"0005865"}}}


id: GO:0042473
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the outer ear are generated and organized. The outer ear is the part of the ear external to the tympanum (eardrum). It consists of a tube (the external auditory meatus) that directs sound waves on to the tympanum, and may also include the external pinna, which extends beyond the skull.","definition_xrefs":["GOC:jl","ISBN:0192801023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"ear morphogenesis","termid":"GO:0042471"}],"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":"outer ear morphogenesis","termid":"GO:0042473"}


id: PBO:0049204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate ionotropic receptor kainate type subunit 4","termid":"PBO:0049204"}


id: PBO:0040206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"astrotactin 2","termid":"PBO:0040206"}


id: SO:0001961
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A modified DNA cytosine base feature, modified by a formyl group at the 5 carbon.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytosine","termid":"SO:0001963"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5_formylcytosine","secondary_identifiers":["http:http\\://www.pacificbiosciences.com/pdf/WP_Detecting_DNA_Base_Modifications_Using_SMRT_Sequencing.pdf"],"synonyms":[{"name":"5-fC","type":"exact"},{"name":"5-formylcytosine","type":"exact"}],"termid":"SO:0001961"}


id: SO:0000094
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene from cyanelle sequence.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"cyanelle_sequence","termid":"SO:0000746"},{"relation_name":"is_a","term_name":"plastid_gene","termid":"SO:0000090"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyanelle_gene","synonyms":[{"name":"cyanelle gene","type":"exact"}],"termid":"SO:0000094"}


id: GO:0160207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of androgen receptor signaling.","definition_xrefs":["PMID:29057879"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of intracellular steroid hormone receptor signaling pathway","termid":"GO:0033145"},{"relation_name":"is_a","term_name":"regulation of androgen receptor signaling pathway","termid":"GO:0060765"},{"relation_name":"positively_regulates","term_name":"androgen receptor signaling pathway","termid":"GO:0030521"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of androgen receptor signaling pathway","termid":"GO:0160207"}


id: MONDO:0002344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete corneal dystrophy (obsolete MONDO:0002344)","termid":"MONDO:0002344","xrefs":{"Monarch":{"xref_id":"0002344"}}}


id: PBO:0082039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-deoxyglucose-6-phosphate phosphatase; member of a family of low molecular weight phosphatases, induced by oxidative and osmotic stress, confers 2-deoxyglucose resistance when overexpressed; DOG2 has a paralog, DOG1, that arose from a single-locus duplication; the last half of DOG1 and DOG2 are subject to gene conversions among S. cerevisiae, S. paradoxus, and S. mikatae","termid":"PBO:0082039"}


id: MONDO:0008918
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Carnitine-acylcarnitine translocase (CACT) deficiency is a life-threatening, inherited disorder of fatty acid oxidation which usually presents in the neonatal period with severe hypoketotic hypoglycemia, hyperammonemia, cardiomyopathy and/or arrhythmia, hepatic dysfunction, skeletal muscle weakness, and encephalopathy.","definition_xrefs":["Orphanet:159"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hypertrophic cardiomyopathy","termid":"MONDO:0005045"},{"relation_name":"excluded_subClassOf","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"disorder of fatty acid oxidation and ketogenesis","termid":"MONDO:0017713"},{"relation_name":"is_a","term_name":"disorder of carnitine cycle and carnitine transport","termid":"MONDO:0017716"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"carnitine-acylcarnitine translocase deficiency","secondary_identifiers":["icd11.foundation:677949122","NANDO:1200972","NANDO:2200511","NCIT:C133086","GARD:1123","DOID:0111585","OMIM:212138","MEDGEN:91000","SCTID:238003000","MESH:C562812","UMLS:C0342791"],"synonyms":[{"name":"CACT deficiency","type":"exact"},{"name":"CACTD","type":"related"},{"name":"CARNITINE-acylcarnitine translocase deficiency","type":"related"},{"name":"Cact deficiency","type":"related"},{"name":"carnitine-acylcarnitine translocase deficiency","type":"exact"}],"termid":"MONDO:0008918","xrefs":{"Monarch":{"xref_id":"0008918"}}}


id: FYPO:0005907
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 nucleus is normal (i.e. indistinguishable from wild type) during a cellular response to heat.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to nucleus during vegetative growth","termid":"FYPO:0000838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0000257","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to nucleus during cellular response to heat","synonyms":[{"name":"normal protein localisation to nucleus during cellular response to heat","type":"exact"},{"name":"normal protein localization to nucleus during cellular response to heat during mitotic cell cycle","type":"related"},{"name":"normal protein localization to nucleus during cellular response to heat during vegetative growth","type":"exact"}],"termid":"FYPO:0005907"}


id: MONDO:0013446
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RPGRIP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Leber congenital amaurosis","termid":"MONDO:0018998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005328"],"is_obsolete":false,"name":"Leber congenital amaurosis 6","secondary_identifiers":["MESH:C565327","GARD:10490","HGNC:13436","ICD10CM:H35.5","MEDGEN:344245","OMIM:613826","DOID:0110329","UMLS:C1854260"],"synonyms":[{"name":"LCA6","type":"exact"},{"name":"Leber congenital amaurosis 6","type":"exact"},{"name":"Leber congenital amaurosis caused by mutation in RPGRIP1","type":"exact"},{"name":"Leber congenital amaurosis type 6","type":"exact"},{"name":"RPGRIP1 Leber congenital amaurosis","type":"exact"}],"termid":"MONDO:0013446","xrefs":{"Monarch":{"xref_id":"0013446"}}}


id: FYPO:0000938
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 cortical microtubule cytoskeleton during interphase of the mitotic cell cycle does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to cell cortex during vegetative growth","termid":"FYPO:0000930"},{"relation_name":"is_a","term_name":"abolished protein localization to microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000934"},{"relation_name":"is_a","term_name":"abnormal protein localization to cortical microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000935"},{"relation_name":"is_a","term_name":"abolished protein localization to cortical microtubule cytoskeleton","termid":"FYPO:0004266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to cortical microtubule cytoskeleton during mitotic interphase","synonyms":[{"name":"abolished protein localisation to cortical microtubule cytoskeleton mitotic interphase during vegetative growth","type":"exact"},{"name":"abolished protein localization to cortical microtubule cytoskeleton during interphase of mitotic cell cycle","type":"exact"},{"name":"protein absent from cortical microtubule cytoskeleton during mitotic interphase","type":"related"},{"name":"protein localization to cortical microtubule cytoskeleton abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0000938"}


id: MONDO:0005615
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Plasmacytoma is a localized mass of neoplastic monoclonal plasma cells that represents approximately 5% of all plasma cell neoplasms. There are two separate entities: primary plasmacytoma of the bone and extramedullary plasmacytoma of the soft tissues. Of the extramedullary plasmacytomas, 80% occur in the head and neck, usually in the upper respiratory tract. The median age at diagnosis is 50 years and the male to female ratio is 3:1. Long-term survival is possible following local radiotherapy, particularly for soft tissue presentations.","definition_xrefs":["Orphanet:86855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma cell neoplasm","termid":"MONDO:0004959"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"plasmacytoma","secondary_identifiers":["DOID:3721","GARD:13446","EFO:0006738","ICD9:238.6","ICDO:9731/3","MEDGEN:18506","MedDRA:10035484","MESH:D010954","SCTID:415112005","icd11.foundation:1811140613","NCIT:C9349","UMLS:C0032131"],"synonyms":[{"name":"anaplastic plasmacytoma","type":"related"},{"name":"anaplastic skeletal plasmacytoma (type)","type":"related"},{"name":"anaplastic solitary extramedullary plasmacytoma of the cecum (type)","type":"related"},{"name":"extramedullary anaplastic plasmacytoma (type)","type":"related"},{"name":"myeloma - solitary","type":"related"},{"name":"myeloma, solitary","type":"related"},{"name":"plasmacytoma","type":"exact"},{"name":"solitary myeloma","type":"related"},{"name":"solitary plasmacytoma","type":"narrow"}],"termid":"MONDO:0005615","xrefs":{"Monarch":{"xref_id":"0005615"}}}


id: PBO:0028198
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_beta-glucanase","termid":"PBO:0028198"}


id: PBO:0055525
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 2959","termid":"PBO:0055525"}


id: PBO:0051215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 5-51","termid":"PBO:0051215"}


id: GO:0005625
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. That fraction of cells, prepared by disruptive biochemical methods, that is soluble in water.","definition_xrefs":["GOC:ma"],"gene_count":0,"genotype_count":0,"name":"obsolete soluble fraction (obsolete GO:0005625)","synonyms":[{"name":"soluble","type":"broad"},{"name":"soluble fraction","type":"exact"}],"termid":"GO:0005625"}


id: PBO:0030227
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_tacrolimus_during_salt_stress","termid":"PBO:0030227"}


id: PBO:0078028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 18","termid":"PBO:0078028"}


id: MONDO:0002436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the nose.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"upper respiratory tract disorder","termid":"MONDO:0004867"},{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nasal disorder","secondary_identifiers":["SCTID:89488007","MESH:D009668","ICD9:478.19","DOID:2825","MEDGEN:10385","UMLS:C0028432"],"synonyms":[{"name":"disease of nose","type":"exact"},{"name":"disease or disorder of nose","type":"exact"},{"name":"disorder of nose","type":"exact"},{"name":"disorder of the nose","type":"exact"},{"name":"nasal disorder","type":"exact"},{"name":"nose disease","type":"exact"},{"name":"nose disease or disorder","type":"exact"}],"termid":"MONDO:0002436","xrefs":{"Monarch":{"xref_id":"0002436"}}}


id: PBO:0067325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 416, pseudogene","termid":"PBO:0067325"}


id: GO:0140836
data:
  {"annotated_genes":["SJAG_00342","SJAG_00150"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96152,107883],"is_not":false,"summary":null,"term":"GO:0140836"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + RNA polymerase II large subunit CTD heptapeptide repeat (consensus YSPTSPS) = ADP + H+ + RNA polymerase II large subunit phosphoserine (position 5).","definition_xrefs":["PMID:28248323"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II CTD heptapeptide repeat kinase activity","termid":"GO:0008353"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00150":null,"SJAG_00342":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016301","GO:0003674","GO:0003824","GO:0140096","GO:0004672","GO:0016740"],"is_obsolete":false,"name":"RNA polymerase II CTD heptapeptide repeat S5 kinase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"RNA polymerase II C-terminal domain S5 kinase activity","type":"exact"}],"termid":"GO:0140836","terms_by_termid":{"GO:0140836":null}}


id: GO:0180033
data:
  {"annotated_genes":["SJAG_00581"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111322],"is_not":false,"summary":null,"term":"GO:0180033"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H4 N6-acetyl-L-lysine (position 8) + H2O = histone H4 L-lysine (position 8) + acetate. This reaction represents the removal of an acetyl group from lysine at position 8 of the histone H4 protein.","definition_xrefs":["PMID:37459529"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H4K deacetylase activity","termid":"GO:0141051"},{"relation_name":"is_a","term_name":"histone deacetylase activity, hydrolytic mechanism","termid":"GO:0141221"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00581":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0033558"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0140096","GO:0033558","GO:0003824","GO:0003674","GO:0016810","GO:0019213"],"is_obsolete":false,"name":"histone H4K8 deacetylase activity, hydrolytic mechanism","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"histone H4K48 deacetylase activity","type":"broad"}],"termid":"GO:0180033","terms_by_termid":{"GO:0180033":null}}


id: PBO:0062346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily K member 5 pseudogene","termid":"PBO:0062346"}


id: GO:0071169
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a protein to a part of a chromosome that is organized into chromatin.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of protein localization to chromosome","termid":"GO:0070199"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"establishment of protein localization to chromatin","synonyms":[{"name":"establishment of protein localisation to chromatin","type":"exact"}],"termid":"GO:0071169"}


id: GO:0010127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions using mycothiol to convert an alkylating agent to an S-conjugate of mycothiol. The latter is cleaved to release mercapturic acid which is excreted from the cell.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detoxification","termid":"GO:0098754"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098754"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"mycothiol-dependent detoxification","synonyms":[{"name":"mycothiol-dependent detoxification of alkylating agent","type":"narrow"}],"termid":"GO:0010127"}


id: GO:0035700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of an astrocyte guided by a specific chemical concentration gradient. Movement may be towards a higher concentration (positive chemotaxis) or towards a lower concentration (negative chemotaxis).","definition_xrefs":["CL:0000127","PMID:12271471","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"astrocyte cell migration","termid":"GO:0043615"},{"relation_name":"is_a","term_name":"cell chemotaxis","termid":"GO:0060326"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"astrocyte chemotaxis","termid":"GO:0035700"}


id: PBO:0065488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome activator subunit 3","termid":"PBO:0065488"}


id: PBO:0039006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALF transcription elongation factor 2","termid":"PBO:0039006"}


id: PBO:0081080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger DHHC-type containing 11B","termid":"PBO:0081080"}


id: PBO:0041037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRCA1 associated protein","termid":"PBO:0041037"}


id: GO:1904008
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 glutamate stimulus.","definition_xrefs":["GO_REF:0000071","PMID:20704590","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete response to monosodium glutamate (obsolete GO:1904008)","termid":"GO:1904008"}


id: PBO:0057260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 486-2","termid":"PBO:0057260"}


id: FYECO:0000027
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiment was performed in the presence of mating pheromone.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000027 presence of mating pheromone (obsolete FYECO:0000027)","termid":"FYECO:0000027"}


id: PBO:0088020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tyrosyl-DNA phosphodiesterase I; hydrolyzes 3' and 5'-phosphotyrosyl bonds; involved in the repair of DNA lesions created by topo I and topo II; mutations in the human homolog, TDP1, result in the a neurodegenerative disease, spinocerebellar ataxia with axonal neuropathy (SCAN1); yeast cells and human rhabdomyosarcoma lines that overexpress TDP1 both exhibit elevated dosage chromosomal instability (dCIN)","termid":"PBO:0088020"}


id: MONDO:0019039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare hemorrhagic disorder due to a constitutional coagulation factors defect (obsolete MONDO:0019039)","secondary_identifiers":["Orphanet:68334"],"synonyms":[{"name":"rare bleeding disorder due to a constitutional coagulation factors defect","type":"exact"},{"name":"rare coagulopathy due to a constitutional coagulation factors defect","type":"exact"}],"termid":"MONDO:0019039","xrefs":{"Monarch":{"xref_id":"0019039"}}}


id: GO:0008603
data:
  {"annotated_genes":["SJAG_01245"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004862"}]},"cv_name":"molecular_function","definition":"Modulation of the activity of the enzyme cAMP-dependent protein kinase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase regulator activity","termid":"GO:0019887"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01245":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0030234","GO:0098772","GO:0003674"],"is_obsolete":false,"name":"cAMP-dependent protein kinase regulator activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"3',5' cAMP-dependent protein kinase regulator activity","type":"exact"},{"name":"3',5'-cAMP-dependent protein kinase regulator activity","type":"exact"},{"name":"adenosine 3',5'-cyclophosphate-dependent protein kinase regulator activity","type":"exact"},{"name":"cAMP-dependent protein kinase, intrinsic regulator activity","type":"narrow"},{"name":"cyclic AMP-dependent protein kinase regulator activity","type":"exact"}],"termid":"GO:0008603","terms_by_termid":{"GO:0004862":null}}


id: GO:0070341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of fat cells by cell division, resulting in the expansion of their population. A fat cell is an animal connective tissue cell specialized for the synthesis and storage of fat.","definition_xrefs":["GOC:mah","GOC:sl"],"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":"fat cell proliferation","synonyms":[{"name":"adipocyte proliferation","type":"exact"},{"name":"adipose cell proliferation","type":"exact"}],"termid":"GO:0070341"}


id: FYPO:0003246
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through S phase of the mitotic cell cycle is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic cell cycle phase","termid":"FYPO:0002740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal mitotic S phase progression","synonyms":[{"name":"normal S phase progression during mitotic cell cycle","type":"exact"},{"name":"normal mitotic S phase progression during vegetative growth","type":"exact"},{"name":"normal mitotic cell cycle progression in S","type":"exact"}],"termid":"FYPO:0003246"}


id: GO:0019884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigen-presenting cell expresses antigen (peptide or lipid) of exogenous origin on its cell surface in association with an MHC protein complex.","definition_xrefs":["PMID:15928678","GOC:add","ISBN:0781735149","PMID:15771591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation","termid":"GO:0019882"}],"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":"antigen processing and presentation of exogenous antigen","synonyms":[{"name":"antigen presentation, exogenous antigen","type":"exact"}],"termid":"GO:0019884"}


id: GO:0042076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The glycosylation of peptidyl-amino acids through a phosphoester bond forming, for example, GlcNAc-alpha-1-P-Ser residues.","definition_xrefs":["PMID:7499424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoprotein biosynthetic process","termid":"GO:0009101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein phosphate-linked glycosylation","synonyms":[{"name":"phosphoglycosylation","type":"exact"},{"name":"protein amino acid phosphate-linked glycosylation","type":"exact"}],"termid":"GO:0042076"}


id: MONDO:0036595
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant sex cord-stromal tumor arising from the ovary. It is characterized by the presence of neoplastic Leydig cells. Signs and symptoms include hirsutism, menorrhagia and metrorrhagia. It may be associated with trisomy 8.","definition_xrefs":["NCIT:C2880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian sertoli-stromal cell tumor","termid":"MONDO:0020807"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian Sertoli-Leydig cell tumor","secondary_identifiers":["MEDGEN:2038","SCTID:254866007","UMLS:C0003810"],"synonyms":[{"name":"Sertoli-Leydig cell tumor of ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumor of the ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumour of ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumour of the ovary","type":"exact"},{"name":"Sertoli-Leydig neoplasm of ovary","type":"exact"},{"name":"Sertoli-Leydig neoplasm of the ovary","type":"exact"},{"name":"androblastoma","type":"exact"},{"name":"arrhenoblastoma","type":"exact"},{"name":"ovarian Sertoli-Leydig cell neoplasm","type":"exact"},{"name":"ovarian Sertoli-Leydig cell tumor","type":"exact"}],"termid":"MONDO:0036595","xrefs":{"Monarch":{"xref_id":"0036595"}}}


id: MONDO:0006758
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mycobacterium infections of the female reproductive tract (genitalia, female).","definition_xrefs":["MESH:D014384"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"female genital tuberculosis","secondary_identifiers":["MEDGEN:21724","SCTID:74181004","EFO:1000935","MedDRA:10061150","UMLS:C0041311"],"termid":"MONDO:0006758","xrefs":{"Monarch":{"xref_id":"0006758"}}}


id: FYPO:0006164
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to linear elements is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to linear element","termid":"FYPO:0000909"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to linear element","synonyms":[{"name":"decreased protein localisation to linear element","type":"exact"},{"name":"reduced protein localization to linear element","type":"exact"}],"termid":"FYPO:0006164"}


id: PBO:0056843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B","termid":"PBO:0056843"}


id: PBO:0050454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homer scaffold protein 2","termid":"PBO:0050454"}


id: FYPO:0003815
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a mitotic cell cycle arrest that normally occurs in response to the S phase DNA damage checkpoint (also known as the intra-S phase DNA damage checkpoint) is decreased. The S phase DNA damage checkpoint slows progression through S phase in response to DNA damage. In a mutant, the checkpoint may fail to arrest or delay cell cycle progression under appropriate conditions, or the incidence or duration of arrest or delay may differ from wild type under any specified set of conditions.","definition_xrefs":["PomBase:mah","GO:0072429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal S-phase DNA damage checkpoint","termid":"FYPO:0000007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0000631","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased response to S-phase DNA damage checkpoint signaling","synonyms":[{"name":"decreased S-phase DNA damage checkpoint during mitotic cell cycle","type":"related"},{"name":"decreased S-phase DNA damage checkpoint during vegetative growth","type":"exact"},{"name":"decreased response to intra-S DNA damage checkpoint signaling","type":"exact"},{"name":"decreased response to mitotic S-phase DNA damage checkpoint signaling","type":"exact"},{"name":"reduced response to intra-S DNA damage checkpoint signaling","type":"exact"}],"termid":"FYPO:0003815"}


id: GO:0047650
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: O-alkylglycerone + ATP = O-alkylglycerone phosphate + ADP + 2 H+.","definition_xrefs":["RHEA:23088","EC:2.7.1.84"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016301","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"alkylglycerone kinase activity","secondary_identifiers":["MetaCyc:ALKYLGLYCERONE-KINASE-RXN","KEGG_REACTION:R03944"],"synonyms":[{"name":"ATP:O-alkylglycerone phosphotransferase activity","type":"related"},{"name":"alkyldihydroxyacetone kinase (phosphorylating)","type":"related"},{"name":"alkyldihydroxyacetone kinase activity","type":"related"}],"termid":"GO:0047650"}


id: GO:0060135
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A reproductive process occurring in the mother that allows an embryo or fetus to develop within it.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal reproductive process","termid":"GO:0048609"},{"relation_name":"part_of","term_name":"female pregnancy","termid":"GO:0007565"}],"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":"maternal process involved in female pregnancy","termid":"GO:0060135"}


id: MONDO:0012512
data:
  {"annotated_genes":["SJAG_05271"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87756],"is_not":false,"summary":null,"term":"MONDO:0012512"}]},"cv_name":"mondo","definition":"Combined oxidative phosphorylation deficiency type 3 is an extremely rare clinically heterogenous disorder described in about 5 patients to date. Clinical signs included hypotonia, lactic acidosis, and hepatic insufficiency, with progressive encephalomyopathy or hypertrophic cardiomyopathy.","definition_xrefs":["Orphanet:168566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05271":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:610505","DOID:0111486","MEDGEN:355842","UMLS:C1864840","SCTID:720951008","MESH:C566467","GARD:17035"],"synonyms":[{"name":"COXPD3","type":"related"},{"name":"TSFM combined oxidative phosphorylation deficiency","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 3","type":"related"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in TSFM","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 3","type":"exact"},{"name":"concentric cardiomyopathy, hypotonia, and lactic acidosis","type":"related"},{"name":"encephalomyopathy, respiratory failure, and lactic acidosis","type":"related"},{"name":"fatal mitochondrial disease due to COXPD3","type":"exact"}],"termid":"MONDO:0012512","terms_by_termid":{"MONDO:0012512":null},"xrefs":{"Monarch":{"xref_id":"0012512"}}}


id: GO:0046965
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nuclear retinoid X receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear retinoic acid receptor binding","termid":"GO:0042974"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"nuclear retinoid X receptor binding","synonyms":[{"name":"RXR binding","type":"exact"},{"name":"retinoid X receptor binding","type":"broad"}],"termid":"GO:0046965"}


id: GO:0047705
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 bilirubin + O2 = 2 biliverdin + 2 H2O.","definition_xrefs":["EC:1.3.3.5","RHEA:20980"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor","termid":"GO:0016634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"bilirubin oxidase activity","secondary_identifiers":["MetaCyc:BILIRUBIN-OXIDASE-RXN","KEGG_REACTION:R02394"],"synonyms":[{"name":"bilirubin oxidase M-1","type":"related"},{"name":"bilirubin:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0047705"}


id: PBO:0028357
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_phosphatase_activity","termid":"PBO:0028357"}


id: PBO:0039774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aquaporin 7","termid":"PBO:0039774"}


id: PBO:0113540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar proteinase B yscB with H3 N-terminal endopeptidase activity; serine protease of subtilisin family; involved in protein degradation in vacuole; required for full protein degradation during sporulation; activity inhibited by Pbi2p; protein abundance increases in response to DNA replication stress; targeted to vacuole via Vps10p-dependent endosomal vacuolar protein sorting pathway and via AP-3 pathway; PRB1 has a paralog, YSP3, that arose from the whole genome duplication","termid":"PBO:0113540"}


id: PBO:0005638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenosine 5'-monophosphoramidase (predicted)","termid":"PBO:0005638"}


id: PBO:0077615
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMSB4X pseudogene 6","termid":"PBO:0077615"}


id: PBO:0059242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L13","termid":"PBO:0059242"}


id: PBO:0091923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA pseudouridine synthase Pus3","termid":"PBO:0091923"}


id: PBO:0074273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schlafen family member 14","termid":"PBO:0074273"}


id: MONDO:0008210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any patterned macular dystrophy in which the cause of the disease is a mutation in the PRPH2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"patterned macular dystrophy","termid":"MONDO:0020381"},{"relation_name":"is_a","term_name":"PRPH2-related retinopathy","termid":"MONDO:1040055"}],"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":"patterned macular dystrophy 1","secondary_identifiers":["DOID:0060866","OMIM:169150","GARD:18237","UMLS:C4551999","MEDGEN:1646806"],"synonyms":[{"name":"MDPT1","type":"exact"},{"name":"PRPH2 patterned macular dystrophy","type":"exact"},{"name":"butterfly dystrophy of retinal pigment epithelium","type":"related"},{"name":"butterfly-shaped pigment dystrophy of the fovea","type":"related"},{"name":"butterfly-shaped pigmentary maculary dystrophy 1","type":"exact"},{"name":"macular dystrophy, butterfly-Shaped pigmentary","type":"related"},{"name":"macular dystrophy, butterfly-shaped pigmentary","type":"exact"},{"name":"macular dystrophy, patterned, 1","type":"related"},{"name":"macular dystrophy, patterned, type 1","type":"exact"},{"name":"patterned dystrophy of retinal pigment epithelium","type":"related"},{"name":"patterned macular dystrophy caused by mutation in PRPH2","type":"exact"},{"name":"patterned macular dystrophy type 1","type":"exact"}],"termid":"MONDO:0008210","xrefs":{"Monarch":{"xref_id":"0008210"}}}


id: PBO:0089813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-H","termid":"PBO:0089813"}


id: PBO:0068557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 8, pseudogene","termid":"PBO:0068557"}


id: PR:O14210
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ies2 gene.","definition_xrefs":["UniProtKB:O14210","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":"INO80 complex subunit 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6B12.05c","synonyms":[{"name":"Spom972h-ies2","type":"exact"}],"termid":"PR:O14210"}


id: MONDO:0018155
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary lateral sclerosis (PLS) is an idiopathic non-familial motor neuron disease characterized by slowly progressive upper motor neuron dysfunction leading to spasticity, mild weakness in voluntary muscle movement, hyperreflexia, and loss of motor speech production.","definition_xrefs":["Orphanet:35689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary motor neuron disease","termid":"MONDO:0024257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"lateral sclerosis","secondary_identifiers":["GARD:10684","MEDGEN:57591","NCIT:C129933","MedDRA:10036704","DOID:230","ICD10CM:G12.23","UMLS:C0154682","NANDO:1200008","icd11.foundation:1686688462","ICD9:335.24","SCTID:81211007"],"synonyms":[{"name":"PLS","type":"exact"},{"name":"adult-onset PLS","type":"exact"},{"name":"adult-onset primary lateral sclerosis","type":"exact"},{"name":"primary lateral sclerosis","type":"exact"}],"termid":"MONDO:0018155","xrefs":{"Monarch":{"xref_id":"0018155"}}}


id: MONDO:0975827
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"orofaciodigital syndrome","termid":"MONDO:0015375"}],"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":"orofaciodigital syndrome 21","secondary_identifiers":["OMIM:301132"],"termid":"MONDO:0975827","xrefs":{"Monarch":{"xref_id":"0975827"}}}


id: FYPO:0007436
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is swollen, is elongated, and contains more than one septum. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated multiseptate vegetative cell","termid":"FYPO:0000223"},{"relation_name":"is_a","term_name":"swollen vegetative cell","termid":"FYPO:0000646"},{"relation_name":"is_a","term_name":"swollen elongated cell","termid":"FYPO:0001429"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000032"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0005447","FYPO:0000631","FYPO:0001985","FYPO:0000032","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"swollen elongated multiseptate vegetative cell","synonyms":[{"name":"elongated swollen multiseptate vegetative cell","type":"exact"},{"name":"swollen elongated multiseptate vegetative cell during mitotic cell cycle","type":"related"},{"name":"swollen elongated multiseptate vegetative cell during vegetative growth","type":"exact"}],"termid":"FYPO:0007436"}


id: FYPO:0002841
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001132"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to a specific location on a chromosome is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization during vegetative growth","termid":"FYPO:0001179"},{"relation_name":"is_a","term_name":"abnormal protein localization to chromosome during vegetative growth","termid":"FYPO:0002838"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null,"SJAG_03892":null},"genotype_count":1,"genotypes_by_uniquename":{"nur1delta__vps4delta":{"display_name":"nur1delta vps4delta","display_uniquename":"nur1delta__vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03892","SJAG_01050"],"name":"abolished protein localization to chromosome during vegetative growth","references_by_uniquename":{"PMID:32109380":null},"synonyms":[{"name":"abolished protein localisation to chromosome during vegetative growth","type":"exact"},{"name":"abolished protein localization to chromosome during mitotic cell cycle","type":"related"},{"name":"protein localization to chromosome abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0002841","terms_by_termid":{"FYPO:0001132":null,"FYPO_EXT:0000001":null}}


id: FYPO:0001426
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which negative regulation of the initiation of mitotic DNA replication is abnormal, resulting in rereplication of part of the genome.","definition_xrefs":["PomBase:mah","PMID:10388806"],"direct_ancestors":[{"relation_name":"has_output","term_name":"DNA content increased during vegetative growth","termid":"FYPO:0000158"},{"relation_name":"is_a","term_name":"abnormal negative regulation of mitotic DNA replication initiation","termid":"FYPO:0000216"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"abnormal negative regulation of mitotic DNA replication initiation resulting in partial rereplication","synonyms":[{"name":"abnormal negative regulation of DNA replication initiation during vegetative growth, resulting in partial rereplication","type":"exact"},{"name":"abnormal negative regulation of DNA replication initiation resulting in partial rereplication during mitotic cell cycle","type":"related"},{"name":"abnormal negative regulation of mitotic DNA replication initiation resulting in partial re-replication","type":"exact"},{"name":"partial mitotic DNA re-replication","type":"related"},{"name":"partial mitotic DNA rereplication","type":"related"},{"name":"replication origin refiring resulting in local amplification","type":"related"}],"termid":"FYPO:0001426"}


id: SO:0001075
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Polypeptide region present in the lipid bilayer.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_structural_region","termid":"SO:0001070"},{"relation_name":"part_of","term_name":"membrane_structure","termid":"SO:0001071"}],"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":"intramembrane_polypeptide_region","secondary_identifiers":["BS:00156"],"synonyms":[{"name":"intramembrane","type":"related"},{"name":"intramembrane polypeptide region","type":"exact"}],"termid":"SO:0001075"}


id: PBO:0001328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxin 13 (predicted)","termid":"PBO:0001328"}


id: MONDO:0009927
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any 3MC syndrome in which the cause of the disease is a mutation in the COLEC11 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3MC syndrome","termid":"MONDO:0017398"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3MC syndrome 2","secondary_identifiers":["Orphanet:2998","MESH:C535586","UMLS:C0796279","EFO:1001977","GARD:18428","DOID:0060576","MEDGEN:167115","OMIM:265050"],"synonyms":[{"name":"3MC syndrome 2","type":"exact"},{"name":"3MC syndrome caused by mutation in COLEC11","type":"exact"},{"name":"3MC syndrome type 2","type":"exact"},{"name":"3MC2","type":"related"},{"name":"3Mc syndrome type 2","type":"exact"},{"name":"COLEC11 3MC syndrome","type":"exact"},{"name":"Carnevale syndrome","type":"related"},{"name":"Carnevale syndrome, formerly","type":"related"},{"name":"Osa syndrome","type":"related"},{"name":"oculo-skeletal-abdominal syndrome","type":"related"},{"name":"ptosis of eyelids with diastasis recti and hip dysplasia","type":"related"}],"termid":"MONDO:0009927","xrefs":{"Monarch":{"xref_id":"0009927"}}}


id: MONDO:0013928
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dystonic disorder in which the cause of the disease is a mutation in the CACNA1B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"focal dystonia","termid":"MONDO:0000477"},{"relation_name":"is_a","term_name":"focal, segmental or multifocal dystonia","termid":"MONDO:0015990"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"dystonia 23","secondary_identifiers":["OMIM:614860","DOID:0090051","UMLS:C3538999","GARD:17694","MEDGEN:761274","Orphanet:420492"],"synonyms":[{"name":"CACNA1B dystonic disorder","type":"exact"},{"name":"DYT23","type":"exact"},{"name":"adult-onset cervical dystonia, DYT23 type","type":"related"},{"name":"dystonia 23","type":"exact"},{"name":"dystonia type 23","type":"exact"},{"name":"dystonic disorder caused by mutation in CACNA1B","type":"exact"}],"termid":"MONDO:0013928","xrefs":{"Monarch":{"xref_id":"0013928"}}}


id: GO:0102722
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-hydroxybutyrate + NAD(P) = 4-oxobutanoate + H+ + NAD(P)H.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gamma-hydroxybutyrate dehydrogenase activity (NAD(P)-dependent (obsolete GO:0102722)","termid":"GO:0102722"}


id: PBO:0016895
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae KNS1","termid":"PBO:0016895"}


id: PBO:0085131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein involved in the asymmetric localization of ASH1 mRNA; binds cooperatively with She2p to the E3 zip-code element in the 3'-UTR of the mRNA; constituent of 66S pre-ribosomal particles involved in pre-rRNA processing and nuclear export of the 60S subunit; may facilitate Rpl43p loading; required post-transcriptionally for efficient retrotransposition; absence results in decreased Ty1 Gag:GFP protein levels; relocalizes from nucleus to cytoplasm upon DNA replication stress","termid":"PBO:0085131"}


id: PBO:0111762
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XP-G family","termid":"PBO:0111762"}


id: MONDO:0012074
data:
  {"annotated_genes":["SJAG_03396"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88438],"is_not":false,"summary":null,"term":"MONDO:0012074"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mandibuloacral dysplasia","termid":"MONDO:0016584"},{"relation_name":"is_a","term_name":"laminopathy","termid":"MONDO:0021106"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03396":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"mandibuloacral dysplasia with type B lipodystrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0081129","UMLS:C1837756","icd11.foundation:1199517264","MESH:C535706","Orphanet:90154","GARD:9989","OMIM:608612","MEDGEN:332940"],"synonyms":[{"name":"MADB","type":"related"},{"name":"MANDIBULOACRAL dysplasia with type B lipodystrophy","type":"related"},{"name":"lipodystrophy, type B, associated with Mandibuloacral dysplasia","type":"related"},{"name":"mandibuloacral dysplasia with type B lipodystrophy","type":"exact"}],"termid":"MONDO:0012074","terms_by_termid":{"MONDO:0012074":null},"xrefs":{"Monarch":{"xref_id":"0012074"}}}


id: PBO:0088171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xanthine-guanine phosphoribosyl transferase; required for xanthine utilization and for optimal utilization of guanine","termid":"PBO:0088171"}


id: MONDO:0009452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare and severe congenital multisystem disorder characterized by the principal features of agenesis of the corpus callosum, cataracts, oculocutaneous hypopigmentation, cardiomyopathy and combined immunodeficiency.","definition_xrefs":["Orphanet:1493"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome associated with dilated cardiomyopathy (obsolete MONDO:0016337)","termid":"MONDO:0016337"},{"relation_name":"excluded_subClassOf","term_name":"hypopigmentation of the skin","termid":"MONDO:0019290"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0006025"],"is_obsolete":false,"name":"Vici syndrome","secondary_identifiers":["UMLS:C1855772","DOID:0060356","MEDGEN:340962","MESH:C535566","SCTID:719824001","NCIT:C138174","GARD:448","OMIM:242840"],"synonyms":[{"name":"Dionisi Vici Sabetta Gambarara syndrome","type":"related"},{"name":"Dionisi-Vici-Sabetta-Gambarara syndrome","type":"exact"},{"name":"VICIS","type":"related"},{"name":"Vici syndrome","type":"exact"},{"name":"absent corpus callosum cataract immunodeficiency","type":"related"},{"name":"absent corpus callosum-cataract-immunodeficiency syndrome","type":"exact"},{"name":"corpus callosum agenesis-cataract-immunodeficiency syndrome","type":"exact"},{"name":"immunodeficiency with cleft Lip/palate, cataract, hypopigmentation, and absent corpus callosum","type":"related"},{"name":"immunodeficiency with cleft lip/palate, cataract, hypopigmentation and absent corpus callosum","type":"related"},{"name":"immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum","type":"exact"}],"termid":"MONDO:0009452","xrefs":{"Monarch":{"xref_id":"0009452"}}}


id: PBO:0110979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD44 molecule (IN blood group)","termid":"PBO:0110979"}


id: PBO:0065339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prune exopolyphosphatase 1","termid":"PBO:0065339"}


id: PBO:0070565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 31","termid":"PBO:0070565"}


id: FYPO:0005774
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 magnesium ions measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"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"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased cellular magnesium level","synonyms":[{"name":"decreased cellular magnesium ion level","type":"exact"},{"name":"decreased cellular magnesium level during mitotic cell cycle","type":"related"},{"name":"decreased cellular magnesium level during vegetative growth","type":"exact"},{"name":"decreased magnesium accumulation","type":"related"},{"name":"reduced cellular magnesium level","type":"exact"}],"termid":"FYPO:0005774"}


id: PBO:0066250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMS3 antisense RNA 3","termid":"PBO:0066250"}


id: PBO:0061628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nudix hydrolase 11","termid":"PBO:0061628"}


id: PBO:0040822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bridging integrator 2","termid":"PBO:0040822"}


id: GO:0043792
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,4,5,6-tetrahydro-6-oxonicotinate + 2 H2O = 2-formylglutarate + NH4.","definition_xrefs":["EC:3.5.2.18","RHEA:17209"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides","termid":"GO:0016812"}],"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:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0016810","GO:0003674"],"is_obsolete":false,"name":"enamidase activity","secondary_identifiers":["MetaCyc:3.5.2.18-RXN","KEGG_REACTION:R07984"],"synonyms":[{"name":"6-oxo-1,4,5,6-tetrahydronicotinate amidohydrolase activity","type":"exact"}],"termid":"GO:0043792"}


id: PBO:0071562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 28","termid":"PBO:0071562"}


id: MONDO:0018227
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypocomplementemic urticarial vasculitis (HUV) is an immune complex-mediated small vessel vasculitis characterized by urticaria and hypocomplementemia (low C1q with or without low C3 and C4), and usually associated with circulating anti-C1q autoantibodies. Arthritis, pulmonary disease, ocular inflammation, and glomerulonephritis are common systemic manifestations.","definition_xrefs":["Orphanet:36412"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"immune complex mediated vasculitis","termid":"MONDO:0015491"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypocomplementemic urticarial vasculitis","secondary_identifiers":["MEDGEN:83360","icd11.foundation:629572966","UMLS:C0343206","SCTID:239945009","GARD:6725"],"synonyms":[{"name":"Mac Duffie hypocomplementemic urticarial vasculitis","type":"exact"},{"name":"Mac Duffie syndrome","type":"exact"},{"name":"McDuffie hypocomplementemic urticarial vasculitis","type":"exact"},{"name":"McDuffie syndrome","type":"exact"},{"name":"anti-C1q vasculitis","type":"exact"}],"termid":"MONDO:0018227","xrefs":{"Monarch":{"xref_id":"0018227"}}}


id: GO:0140124
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of Lewy body formation.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of inclusion body assembly","termid":"GO:0090261"},{"relation_name":"is_a","term_name":"regulation of Lewy body formation","termid":"GO:0140122"},{"relation_name":"positively_regulates","term_name":"Lewy body formation","termid":"GO:0140121"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of Lewy body formation","termid":"GO:0140124"}


id: PBO:0083329
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; overlaps ORF STE20/YHL007C","termid":"PBO:0083329"}


id: PBO:0028896
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_telomere_maintenance","termid":"PBO:0028896"}


id: PBO:0039732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein C3","termid":"PBO:0039732"}


id: GO:1990361
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex capable of pyruvate kinase activity. PKM2 only exists as homotetramer when bound to beta-d-fructofuranose 1,6-bisphosphate (CHEBI:28013).","definition_xrefs":["PMID:24606918","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate kinase complex","termid":"GO:1902912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"PKM2 pyruvate kinase complex","synonyms":[{"name":"PKM2 homotetramer","type":"exact"}],"termid":"GO:1990361"}


id: MOD:00194
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to an amino-terminal lactic acid.","definition_xrefs":["Unimod:403#S","PubMed:7607233","RESID:AA0186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactic acid","synonyms":[{"name":"(2R)-2-hydroxypropanoic acid","type":"exact"},{"name":"2-hydroxypropionic acid","type":"exact"},{"name":"Lac(Ser)","type":"exact"},{"name":"MOD_RES Lactic acid","type":"exact"},{"name":"Ser->LacticAcid","type":"related"},{"name":"alpha-hydroxypropionic acid","type":"exact"},{"name":"lactic acid","type":"exact"},{"name":"lactic acid from N-term Ser","type":"related"}],"termid":"MOD:00194"}


id: PBO:0028687
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_DNA_double-strand_break_formation","termid":"PBO:0028687"}


id: MONDO:0002886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the common bile duct.","direct_ancestors":[{"relation_name":"is_a","term_name":"bile duct disorder","termid":"MONDO:0002887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"common bile duct disorder","secondary_identifiers":["MEDGEN:3545","MESH:D003137","DOID:4137","UMLS:C0009440"],"synonyms":[{"name":"common bile duct disease","type":"exact"},{"name":"common bile duct disease or disorder","type":"exact"},{"name":"disease of common bile duct","type":"exact"},{"name":"disease or disorder of common bile duct","type":"exact"},{"name":"disorder of common bile duct","type":"exact"}],"termid":"MONDO:0002886","xrefs":{"Monarch":{"xref_id":"0002886"}}}


id: PBO:0003030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human COMT ortholog 2","termid":"PBO:0003030"}


id: PBO:0049508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 15","termid":"PBO:0049508"}


id: GO:0051668
data:
  {"annotated_genes":["SJAG_00360","SJAG_03440","SJAG_02361","SJAG_02757","SJAG_00959","SJAG_00405","SJAG_04846","SJAG_04565","SJAG_03515","SJAG_00299","SJAG_00895","SJAG_03453","SJAG_03955","SJAG_05300","SJAG_03865","SJAG_03315","SJAG_01405","SJAG_02588","SJAG_03838","SJAG_02456","SJAG_01917","SJAG_01999","SJAG_00916","SJAG_02240","SJAG_01223","SJAG_04129","SJAG_02282","SJAG_01782","SJAG_02065","SJAG_02524","SJAG_01382","SJAG_01299","SJAG_03810","SJAG_03633","SJAG_04923","SJAG_00277","SJAG_01178","SJAG_03502","SJAG_05414","SJAG_02034","SJAG_03029","SJAG_00669","SJAG_04509","SJAG_04996","SJAG_02914","SJAG_04451","SJAG_03250","SJAG_00826","SJAG_03756","SJAG_05302","SJAG_02753","SJAG_04609","SJAG_03864","SJAG_00175","SJAG_01951","SJAG_01558","SJAG_03684","SJAG_02208","SJAG_02354","SJAG_00603","SJAG_02437","SJAG_03416","SJAG_04294","SJAG_03938","SJAG_01759","SJAG_02797","SJAG_01809","SJAG_00430","SJAG_03930","SJAG_04158","SJAG_01240","SJAG_00330","SJAG_01940","SJAG_01120","SJAG_01112","SJAG_00404","SJAG_03754","SJAG_01640","SJAG_03396","SJAG_01945","SJAG_04044","SJAG_00102","SJAG_02392","SJAG_01282","SJAG_03915","SJAG_04763","SJAG_01641","SJAG_01949","SJAG_02210","SJAG_04930","SJAG_00144","SJAG_03781","SJAG_03970","SJAG_01135","SJAG_01445","SJAG_01733","SJAG_01435","SJAG_01349","SJAG_01516","SJAG_02320","SJAG_01840","SJAG_04208","SJAG_00687","SJAG_02811","SJAG_04597","SJAG_04434","SJAG_01127","SJAG_00314","SJAG_00858","SJAG_01335","SJAG_00569","SJAG_01114","SJAG_02736","SJAG_02355","SJAG_04358","SJAG_01367","SJAG_02330","SJAG_02912","SJAG_02583","SJAG_00379","SJAG_04203","SJAG_01780","SJAG_04684","SJAG_03411","SJAG_00064","SJAG_01496"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99724,109135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006613"},{"annotations":[82057,81841,74833,76518,117586,74857,117508,81218,81379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032456"},{"annotations":[67803,120765,61966,114643,93104,96713,102947,114860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099638"},{"annotations":[97531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061951"},{"annotations":[102834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140569"},{"annotations":[76427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140570"},{"annotations":[108875,108246,110637,96966,79334,111426,114862,71926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043001"},{"annotations":[77755,101577,74340,102668,79126,108124,57675,109222,94084,72430,73663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006893"},{"annotations":[118791,104742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140043"},{"annotations":[89903],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0042997"},{"annotations":[96221],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0140325"},{"annotations":[97670],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903077"},{"annotations":[97550,81253,111183,111472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006620"},{"annotations":[81991,99145,110150,74905,99861],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031204"},{"annotations":[113245,92238,97244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045046"},{"annotations":[99862,110238,100405,106304,115697,100173,110151,112249,107998,69308,105330,111184,96649,116251,103010,93485,114108,106612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045048"},{"annotations":[104745,77448,75175,75719,118126,58495,79524,90470,109424],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[76218,80350,80289,58620,80031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032979"},{"annotations":[100043,113645,71687,111893,78347,59123,109401,112246,100394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045040"},{"annotations":[79879,79197,73677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072657"},{"annotations":[76878,78691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036228"},{"annotations":[91346,92363,97532,92661,66755,103222,116814,69857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072659"},{"annotations":[97715,72791,74676,76776,76611,60746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006612"},{"annotations":[92815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044395"},{"annotations":[89712],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2001135"},{"annotations":[111473,67598,96089,70543,74709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006614"},{"annotations":[116229,93447,116990],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006617"},{"annotations":[75366,74957,77296,110152,99863,104404],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006616"},{"annotations":[89738,116954,74549,76806,115987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071816"}]},"cv_name":"biological_process","definition":"Any process in which a substance or cellular entity, such as a protein complex or organelle, is transported to, and/or maintained in, a specific location within a membrane.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular localization","termid":"GO:0051641"}],"gene_count":126,"genes_by_uniquename":{"SJAG_00064":null,"SJAG_00102":null,"SJAG_00144":null,"SJAG_00175":null,"SJAG_00277":null,"SJAG_00299":null,"SJAG_00314":null,"SJAG_00330":null,"SJAG_00360":null,"SJAG_00379":null,"SJAG_00404":null,"SJAG_00405":null,"SJAG_00430":null,"SJAG_00569":null,"SJAG_00603":null,"SJAG_00669":null,"SJAG_00687":null,"SJAG_00826":null,"SJAG_00858":null,"SJAG_00895":null,"SJAG_00916":null,"SJAG_00959":null,"SJAG_01112":null,"SJAG_01114":null,"SJAG_01120":null,"SJAG_01127":null,"SJAG_01135":null,"SJAG_01178":null,"SJAG_01223":null,"SJAG_01240":null,"SJAG_01282":null,"SJAG_01299":null,"SJAG_01335":null,"SJAG_01349":null,"SJAG_01367":null,"SJAG_01382":null,"SJAG_01405":null,"SJAG_01435":null,"SJAG_01445":null,"SJAG_01496":null,"SJAG_01516":null,"SJAG_01558":null,"SJAG_01640":null,"SJAG_01641":null,"SJAG_01733":null,"SJAG_01759":null,"SJAG_01780":null,"SJAG_01782":null,"SJAG_01809":null,"SJAG_01840":null,"SJAG_01917":null,"SJAG_01940":null,"SJAG_01945":null,"SJAG_01949":null,"SJAG_01951":null,"SJAG_01999":null,"SJAG_02034":null,"SJAG_02065":null,"SJAG_02208":null,"SJAG_02210":null,"SJAG_02240":null,"SJAG_02282":null,"SJAG_02320":null,"SJAG_02330":null,"SJAG_02354":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_02392":null,"SJAG_02437":null,"SJAG_02456":null,"SJAG_02524":null,"SJAG_02583":null,"SJAG_02588":null,"SJAG_02736":null,"SJAG_02753":null,"SJAG_02757":null,"SJAG_02797":null,"SJAG_02811":null,"SJAG_02912":null,"SJAG_02914":null,"SJAG_03029":null,"SJAG_03250":null,"SJAG_03315":null,"SJAG_03396":null,"SJAG_03411":null,"SJAG_03416":null,"SJAG_03440":null,"SJAG_03453":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03633":null,"SJAG_03684":null,"SJAG_03754":null,"SJAG_03756":null,"SJAG_03781":null,"SJAG_03810":null,"SJAG_03838":null,"SJAG_03864":null,"SJAG_03865":null,"SJAG_03915":null,"SJAG_03930":null,"SJAG_03938":null,"SJAG_03955":null,"SJAG_03970":null,"SJAG_04044":null,"SJAG_04129":null,"SJAG_04158":null,"SJAG_04203":null,"SJAG_04208":null,"SJAG_04294":null,"SJAG_04358":null,"SJAG_04434":null,"SJAG_04451":null,"SJAG_04509":null,"SJAG_04565":null,"SJAG_04597":null,"SJAG_04609":null,"SJAG_04684":null,"SJAG_04763":null,"SJAG_04846":null,"SJAG_04923":null,"SJAG_04930":null,"SJAG_04996":null,"SJAG_05300":null,"SJAG_05302":null,"SJAG_05414":null},"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":"localization within membrane","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"establishment and maintenance of localization in membrane","type":"exact"},{"name":"establishment and maintenance of position in membrane","type":"exact"},{"name":"localisation within membrane","type":"exact"},{"name":"localization to membrane","type":"exact"},{"name":"positioning within membrane","type":"narrow"}],"termid":"GO:0051668","terms_by_termid":{"GO:0006612":null,"GO:0006613":null,"GO:0006614":null,"GO:0006616":null,"GO:0006617":null,"GO:0006620":null,"GO:0006893":null,"GO:0031204":null,"GO:0032456":null,"GO:0032979":null,"GO:0036228":null,"GO:0042997":null,"GO:0043001":null,"GO:0044395":null,"GO:0045039":null,"GO:0045040":null,"GO:0045046":null,"GO:0045048":null,"GO:0061951":null,"GO:0071816":null,"GO:0072657":null,"GO:0072659":null,"GO:0099638":null,"GO:0140043":null,"GO:0140325":null,"GO:0140569":null,"GO:0140570":null,"GO:1903077":null,"GO:2001135":null}}


id: GO:0048933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an afferent axon in the posterior lateral line nerve over time from its formation to the mature structure. This process includes axonogenesis and pathfinding of the afferent axons in the posterior lateral line nerve.","definition_xrefs":["PMID:15018940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"afferent axon development in lateral line nerve","termid":"GO:0048893"},{"relation_name":"part_of","term_name":"posterior lateral line nerve development","termid":"GO:0048918"}],"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":"afferent axon development in posterior lateral line nerve","termid":"GO:0048933"}


id: GO:0097512
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cardiac myofibril is a myofibril specific to cardiac muscle cells.","definition_xrefs":["GOC:cjm","GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myofibril","termid":"GO:0030016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cardiac myofibril","termid":"GO:0097512"}


id: MONDO:0014954
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome, periodontitis type","termid":"MONDO:0007527"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ehlers-Danlos syndrome, periodontal type 2","secondary_identifiers":["DOID:0080987","GARD:16209","OMIM:617174","UMLS:C4310681","MEDGEN:934648"],"synonyms":[{"name":"EDSPD2","type":"related"},{"name":"Ehlers-Danlos syndrome, periodontal type, 2","type":"related"}],"termid":"MONDO:0014954","xrefs":{"Monarch":{"xref_id":"0014954"}}}


id: PATO:0000123
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000123 absolute length (obsolete PATO:0000123)","termid":"PATO:0000123"}


id: MONDO:0012906
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAI2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 9","secondary_identifiers":["MESH:C567310","UMLS:C2676235","OMIM:612444","DOID:0110622","GARD:15558","MEDGEN:390990"],"synonyms":[{"name":"CILD9","type":"exact"},{"name":"DNAI2 primary ciliary dyskinesia","type":"exact"},{"name":"ciliary dyskinesia, primary, 9","type":"related"},{"name":"ciliary dyskinesia, primary, 9, with or without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 9","type":"exact"},{"name":"primary ciliary dyskinesia 9","type":"exact"},{"name":"primary ciliary dyskinesia 9 with or without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in DNAI2","type":"exact"},{"name":"primary ciliary dyskinesia type 9","type":"exact"}],"termid":"MONDO:0012906","xrefs":{"Monarch":{"xref_id":"0012906"}}}


id: PBO:0002523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase (predicted)","termid":"PBO:0002523"}


id: GO:1900458
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of brassinosteroid mediated signaling pathway.","definition_xrefs":["PMID:21855796","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of brassinosteroid mediated signaling pathway","termid":"GO:1900457"},{"relation_name":"negatively_regulates","term_name":"brassinosteroid mediated signaling pathway","termid":"GO:0009742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of brassinosteroid mediated signaling pathway","synonyms":[{"name":"down regulation of brassinosteroid mediated signaling pathway","type":"exact"},{"name":"down regulation of brassinosteroid mediated signalling","type":"exact"},{"name":"down-regulation of brassinosteroid mediated signaling pathway","type":"exact"},{"name":"down-regulation of brassinosteroid mediated signalling","type":"exact"},{"name":"downregulation of brassinosteroid mediated signaling pathway","type":"exact"},{"name":"downregulation of brassinosteroid mediated signalling","type":"exact"},{"name":"inhibition of brassinosteroid mediated signaling pathway","type":"narrow"},{"name":"inhibition of brassinosteroid mediated signalling","type":"exact"},{"name":"negative regulation of brassinosteroid mediated signalling","type":"exact"}],"termid":"GO:1900458"}


id: PBO:0074760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 119","termid":"PBO:0074760"}


id: GO:0047168
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: caffeoyl-CoA + isocitrate = 2-caffeoylisocitrate + CoA.","definition_xrefs":["RHEA:20756","EC:2.3.1.126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016746","GO:0016740"],"is_obsolete":false,"name":"isocitrate O-dihydroxycinnamoyltransferase activity","secondary_identifiers":["KEGG_REACTION:R01946","MetaCyc:2.3.1.126-RXN"],"synonyms":[{"name":"caffeoyl-CoA:isocitrate 3-O-(3,4-dihydroxycinnamoyl)transferase activity","type":"related"}],"termid":"GO:0047168"}


id: PBO:0062710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily H member 2 pseudogene","termid":"PBO:0062710"}


id: PBO:0060448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEDD8 activating enzyme E1 subunit 1","termid":"PBO:0060448"}


id: PR:O74791
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A guanine nucleotide-binding protein-like 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03930","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":"GTPase grn1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC26H8.08c","secondary_identifiers":["UniProtKB:O74791"],"synonyms":[{"name":"GTPase in ribosomal export from the nucleolus protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-GNL3","type":"exact"},{"name":"nuclear GTP-binding protein grn1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74791"}


id: PBO:0085981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; protein-protein interactions suggest a possible role in actin patch formation; YNR065C is not an essential gene","termid":"PBO:0085981"}


id: PR:O74315
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- amo1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74315"],"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":"nucleoporin-like protein amo1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC15D4.10c","synonyms":[{"name":"Spom972h-amo1","type":"exact"},{"name":"aberrant microtubule protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74315"}


id: PBO:0084130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hexokinase isoenzyme 2; phosphorylates glucose in cytosol; predominant hexokinase during growth on glucose; represses expression of HXK1, GLK1, induces expression of its own gene; antiapoptotic; phosphorylation/dephosphorylation at Ser14 by kinase Snf1p, phosphatase Glc7p-Reg1p regulates nucleocytoplasmic shuttling of Hxk2p; functions downstream of Sit4p in control of cell cycle, mitochondrial function, oxidative stress resistance, chronological lifespan; has paralog HXK1","termid":"PBO:0084130"}


id: PBO:0049592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 clustered histone 10","termid":"PBO:0049592"}


id: GO:0050497
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of an alkylthio group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:ai","EC:2.8.4.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring sulphur-containing groups","termid":"GO:0016782"}],"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:0016782"}],"interesting_parent_ids":["GO:0016782","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"alkylthioltransferase activity","synonyms":[{"name":"transferase activity, transferring alkylthio groups","type":"exact"}],"termid":"GO:0050497"}


id: FYPO:0007502
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the meiotic spindle pole body is decreased during prophase of the first meiotic nuclear division.","definition_xrefs":["PMID:16111942","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to meiotic spindle pole body during meiosis I","termid":"FYPO:0007482"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0000054","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein localization to meiotic spindle pole body during prophase I","synonyms":[{"name":"decreased protein localisation to meiotic spindle pole body during prophase I","type":"exact"},{"name":"decreased protein localization to meiotic SPB during prophase I","type":"exact"},{"name":"decreased protein localization to meiotic spindle pole body during meiotic prophase I","type":"exact"},{"name":"decreased protein localization to meiotic spindle pole body during prophase of first meiotic nuclear division","type":"exact"},{"name":"decreased protein localization to spindle pole body during prophase I","type":"exact"},{"name":"reduced protein localization to meiotic spindle pole body during prophase I","type":"exact"}],"termid":"FYPO:0007502"}


id: MONDO:0020059
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete gonosome number anomaly (obsolete MONDO:0020059)","secondary_identifiers":["Orphanet:98156"],"synonyms":[{"name":"Sex-chromosome number anomaly","type":"exact"}],"termid":"MONDO:0020059","xrefs":{"Monarch":{"xref_id":"0020059"}}}


id: MONDO:0044907
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma which has spread from its original site of growth to another anatomic site.","definition_xrefs":["NCIT:C4104"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"metastatic carcinoma","termid":"MONDO:0024879"}],"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":"metastatic squamous cell carcinoma","secondary_identifiers":["MEDGEN:90749","SCTID:403906006","UMLS:C0334246"],"synonyms":[{"name":"Metastatic squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0044907","xrefs":{"Monarch":{"xref_id":"0044907"}}}


id: FYPO:0006912
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing clomiphene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000257","FYPO:0000139","FYPO:0002060","FYPO:0002058","FYPO:0000003"],"is_obsolete":false,"name":"normal growth on clomiphene","synonyms":[{"name":"normal cell population growth in presence of clomiphene","type":"exact"},{"name":"normal cell population growth on clomiphene","type":"exact"},{"name":"normal cellular response to clomiphene","type":"related"},{"name":"normal vegetative cell population growth on clomiphene","type":"exact"}],"termid":"FYPO:0006912"}


id: GO:0047847
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2'-deoxyuridine + phosphate = 2-deoxy-alpha-D-ribose 1-phosphate + uracil.","definition_xrefs":["RHEA:22824"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine-nucleoside phosphorylase activity","termid":"GO:0016154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016757","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"deoxyuridine phosphorylase activity","secondary_identifiers":["MetaCyc:URA-PHOSPH-RXN"],"termid":"GO:0047847"}


id: PATO:0001179
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001179 immune (obsolete PATO:0001179)","termid":"PATO:0001179"}


id: PBO:0117235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malate transmembrane transporter family","termid":"PBO:0117235"}


id: GO:0050463
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: nitrite + NAD(P)+ + H2O = nitrate + NAD(P)H + H+.","definition_xrefs":["EC:1.7.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrate reductase activity","termid":"GO:0008940"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor","termid":"GO:0046857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"nitrate reductase [NAD(P)H] activity","synonyms":[{"name":"NAD(P)H bispecific nitrate reductase activity","type":"related"},{"name":"NAD(P)H-nitrate reductase activity","type":"related"},{"name":"NAD(P)H2:nitrate oxidoreductase activity","type":"related"},{"name":"NAD(P)H:nitrate oxidoreductase activity","type":"related"},{"name":"assimilatory NAD(P)H-nitrate reductase activity","type":"related"},{"name":"assimilatory nitrate reductase activity","type":"related"},{"name":"nitrate reductase (reduced nicotinamide adenine dinucleotide (phosphate)) activity","type":"related"},{"name":"nitrate reductase NAD(P)H activity","type":"related"},{"name":"nitrate reductase [NAD(P)H2]","type":"related"},{"name":"nitrite:NAD(P)+ oxidoreductase activity","type":"related"}],"termid":"GO:0050463"}


id: PBO:0054866
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 2280","termid":"PBO:0054866"}


id: PBO:0057289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 509-1","termid":"PBO:0057289"}


id: MOD:01234
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label - alkaline phosphatase to dephosphorylate","definition_xrefs":["Unimod:258#S","PubMed:11467524"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(18)O monosubstituted residue","termid":"MOD:00581"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(18)O monosubstituted L-serine","synonyms":[{"name":"Label:18O(1)","type":"related"},{"name":"O18 Labeling","type":"related"}],"termid":"MOD:01234"}


id: MONDO:0859265
data:
  {"annotated_genes":["SJAG_00516"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88643],"is_not":false,"summary":null,"term":"MONDO:0859265"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00516":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with epilepsy and brain atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619971","UMLS:C5774184","MEDGEN:1823957"],"termid":"MONDO:0859265","terms_by_termid":{"MONDO:0859265":null},"xrefs":{"Monarch":{"xref_id":"0859265"}}}


id: PBO:0040895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMPR1B divergent transcript","termid":"PBO:0040895"}


id: PBO:0088460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fumble family pantothenate kinase","termid":"PBO:0088460"}


id: GO:0004578
data:
  {"annotated_genes":["SJAG_02102"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[69630],"is_not":false,"summary":null,"term":"GO:0004578"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: an N,N'-diacetylchitobiosyl-diphospho-di-trans,poly-cis-dolichol + GDP-alpha-D-mannose = a beta-D-Man-(1->4)-beta-D-GlcNAc-(1->4)-alpha-D-GlcNAc-diphospho-di-trans,poly-cis-dolichol + GDP + H+.","definition_xrefs":["RHEA:13865"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-1,4-mannosyltransferase activity","termid":"GO:0019187"},{"relation_name":"is_a","term_name":"GlcNAc(2)-PP-Dol mannosyltransferase activity","termid":"GO:0120562"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02102":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016757"],"is_obsolete":false,"name":"chitobiosyldiphosphodolichol beta-mannosyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["Reactome:R-HSA-446218","Reactome:R-HSA-4549382","EC:2.4.1.142","MetaCyc:2.4.1.142-RXN"],"synonyms":[{"name":"GDP-mannose-dolichol diphosphochitobiose mannosyltransferase activity","type":"related"},{"name":"GDP-mannose:chitobiosyldiphosphodolichol beta-D-mannosyltransferase activity","type":"related"},{"name":"guanosine diphosphomannose-dolichol diphosphochitobiose mannosyltransferase activity","type":"related"}],"termid":"GO:0004578","terms_by_termid":{"GO:0004578":null}}


id: PBO:0072023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S8 pseudogene 10","termid":"PBO:0072023"}


id: GO:0099523
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of the cytosol consisting of all cytosol that is part of the presynapse.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytosolic region","termid":"GO:0099522"},{"relation_name":"part_of","term_name":"presynapse","termid":"GO:0098793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005829"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005829"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005829","GO:0005575"],"is_obsolete":false,"name":"presynaptic cytosol","termid":"GO:0099523"}


id: GO:1900468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of phosphatidylserine biosynthetic process.","definition_xrefs":["PMID:8056324","GOC:dgf","PMID:8614637","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phospholipid biosynthetic process","termid":"GO:0071071"},{"relation_name":"is_a","term_name":"regulation of phosphatidylserine metabolic process","termid":"GO:0150178"},{"relation_name":"regulates","term_name":"phosphatidylserine biosynthetic process","termid":"GO:0006659"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of phosphatidylserine biosynthetic process","synonyms":[{"name":"regulation of phosphatidylserine anabolism","type":"exact"},{"name":"regulation of phosphatidylserine biosynthesis","type":"exact"},{"name":"regulation of phosphatidylserine formation","type":"exact"},{"name":"regulation of phosphatidylserine synthesis","type":"exact"}],"termid":"GO:1900468"}


id: PBO:0075063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 116-26","termid":"PBO:0075063"}


id: PBO:0030409
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-substance_absent_from_cell_during_vegetative_growth","termid":"PBO:0030409"}


id: PBO:0054201
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 1581","termid":"PBO:0054201"}


id: PBO:0038564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABITRAM pseudogene 1","termid":"PBO:0038564"}


id: MONDO:0054776
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial focal epilepsy with variable foci","termid":"MONDO:0020310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"epilepsy, familial focal, with variable foci 4","secondary_identifiers":["OMIM:617935","DOID:0081424","UMLS:C4693694","MEDGEN:1644614"],"synonyms":[{"name":"FFEVF4","type":"related"},{"name":"epilepsy, FAMILIAL focal, with variable foci 4","type":"related"}],"termid":"MONDO:0054776","xrefs":{"Monarch":{"xref_id":"0054776"}}}


id: MONDO:0010439
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":"cardiomyopathy, fatal fetal, due to myocardial calcification","secondary_identifiers":["UMLS:C1853577","OMIM:300829","MEDGEN:340013","MESH:C543241","OMIM:606163"],"synonyms":[{"name":"cardiomyopathy, fatal fetal, due to myocardial calcification","type":"exact"},{"name":"myocardial calcifications resulting in intrauterine fetal death","type":"related"},{"name":"myocardial calcifications resulting in intrauterine foetal death","type":"related"}],"termid":"MONDO:0010439","xrefs":{"Monarch":{"xref_id":"0010439"}}}


id: PR:Q9Y7S5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC569.06 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7S5"],"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 C569.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC569.06","synonyms":[{"name":"Spom972h-SPCC569.06","type":"exact"}],"termid":"PR:Q9Y7S5"}


id: GO:2000138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell proliferation involved in heart morphogenesis.","definition_xrefs":["GOC:dph"],"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 cell proliferation involved in heart morphogenesis","termid":"GO:2000136"},{"relation_name":"positively_regulates","term_name":"cell proliferation involved in heart morphogenesis","termid":"GO:0061323"}],"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 cell proliferation involved in heart morphogenesis","termid":"GO:2000138"}


id: RO:0002231
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x 'has starts location' y if and only if there exists some process z such that x 'starts with' z and z 'occurs in' y","direct_ancestors":[{"relation_name":"is_a","term_name":"has_part_that_occurs_in","termid":"RO:0002479"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_start_location","termid":"RO:0002231"}


id: PBO:0071136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22","termid":"PBO:0071136"}


id: PR:000028938
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An AP-1-like transcription factor reduced form in Schizosaccharomyces pombe.","definition_xrefs":["PRO:CNA","PMID:22245228"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AP-1-like transcription factor","termid":"PR:000027897"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-1-like transcription factor reduced form (Schizosaccharomyces pombe)","pombase_gene_id":"SPAC1783.07c","synonyms":[{"name":"Spom-pap1/Red+","type":"exact"}],"termid":"PR:000028938"}


id: GO:1904877
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of DNA ligase activity.","definition_xrefs":["GOC:BHF","GOC:rl","GO_REF:0000059","GOC:TermGenie","GOC:BHF_telomere","PMID:17389648"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of DNA ligase activity (obsolete GO:1904877)","synonyms":[{"name":"activation of DNA ligase activity","type":"narrow"},{"name":"up regulation of DNA ligase activity","type":"exact"},{"name":"up-regulation of DNA ligase activity","type":"exact"},{"name":"upregulation of DNA ligase activity","type":"exact"}],"termid":"GO:1904877"}


id: MOD:00311
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to L-cysteine coenzyme A disulfide.","definition_xrefs":["RESID:AA0306","Unimod:281#C","DeltaMass:0","PubMed:1734967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"disulfide conjugated residue","termid":"MOD:01862"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-cysteine coenzyme A disulfide","synonyms":[{"name":"(2R)-2-amino-3-(2-((3-(((2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)amino)-1-oxopropyl)amino)ethyl)dithio-propanoic acid 4'-ester with adenosine 5'-(trihydrogen diphosphate) 3'-(dihydrogen phosphate)","type":"exact"},{"name":"CoenzymeA","type":"related"},{"name":"Cysteine modified Coenzyme A","type":"related"},{"name":"L-cysteine coenzyme A disulfide","type":"exact"},{"name":"SCoACys","type":"exact"},{"name":"coenzyme A L-cysteine mixed disulfide","type":"exact"}],"termid":"MOD:00311"}


id: MONDO:0009142
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":"dystonia with Ringbinden","secondary_identifiers":["UMLS:C1857089","MEDGEN:346509","OMIM:224550","MESH:C565608"],"synonyms":[{"name":"dystonia with Ringbinden","type":"exact"}],"termid":"MONDO:0009142","xrefs":{"Monarch":{"xref_id":"0009142"}}}


id: GO:0016351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete drug susceptibility/resistance (obsolete GO:0016351)","synonyms":[{"name":"drug susceptibility/resistance","type":"exact"}],"termid":"GO:0016351"}


id: GO:0102392
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: decanoate + ATP(4-) + an HmqF protein = AMP(2-) + diphosphoric acid + a decanoyl-HmqF protein.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete decanoate-[HmqF protein] ligase activity (obsolete GO:0102392)","termid":"GO:0102392"}


id: GO:0015802
data:
  {"annotated_genes":["SJAG_02716","SJAG_04715","SJAG_02029","SJAG_03400","SJAG_01336","SJAG_04725","SJAG_00877","SJAG_01923","SJAG_04983","SJAG_01636","SJAG_03256","SJAG_00051"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92206],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034488"},{"annotations":[96405],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034490"},{"annotations":[105842,99150,105841,105843,105844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990822"},{"annotations":[105648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090518"},{"annotations":[100637,64362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903826"},{"annotations":[99165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0089708"},{"annotations":[105651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090513"},{"annotations":[105652,111873,104623],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090517"}]},"cv_name":"biological_process","definition":"The directed movement of basic amino acids, amino acids with a pH above 7, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid transport","termid":"GO:0006865"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00051":null,"SJAG_00877":null,"SJAG_01336":null,"SJAG_01636":null,"SJAG_01923":null,"SJAG_02029":null,"SJAG_02716":null,"SJAG_03256":null,"SJAG_03400":null,"SJAG_04715":null,"SJAG_04725":null,"SJAG_04983":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"basic amino acid transport","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"termid":"GO:0015802","terms_by_termid":{"GO:0034488":null,"GO:0034490":null,"GO:0089708":null,"GO:0090513":null,"GO:0090517":null,"GO:0090518":null,"GO:1903826":null,"GO:1990822":null}}


id: MONDO:0018772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Joubert syndrome (JS) is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones.","definition_xrefs":["Orphanet:475"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete malformation of the cerebellar vermis (obsolete MONDO:0020130)","termid":"MONDO:0020130"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"ciliopathy","termid":"MONDO:0005308"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome","secondary_identifiers":["DOID:0050777","NCIT:C74996","icd11.foundation:1414756318","NORD:1312","UMLS:C0431399","OMIMPS:213300","GARD:6802","SCTID:716997004","MEDGEN:98464"],"synonyms":[{"name":"CPD IV","type":"exact"},{"name":"JBTS","type":"exact"},{"name":"Joubert syndrome","type":"exact"},{"name":"Joubert syndrome type A","type":"exact"},{"name":"Joubert-Boltshauser syndrome","type":"exact"},{"name":"cerebellar vermis agenesis","type":"related"},{"name":"cerebelloparenchymal disorder IV","type":"exact"},{"name":"classic Joubert syndrome","type":"exact"},{"name":"pure Joubert syndrome","type":"exact"}],"termid":"MONDO:0018772","xrefs":{"Monarch":{"xref_id":"0018772"}}}


id: GO:0009840
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A Clp endopeptidase complex located in the chloroplast.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endopeptidase Clp complex","termid":"GO:0009368"},{"relation_name":"part_of","term_name":"chloroplast stroma","termid":"GO:0009570"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"chloroplastic endopeptidase Clp complex","termid":"GO:0009840"}


id: PBO:0059796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 22","termid":"PBO:0059796"}


id: PBO:0075232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 5 pseudogene 2","termid":"PBO:0075232"}


id: PBO:0066812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 111","termid":"PBO:0066812"}


id: PBO:0078484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon AAT) 5-4","termid":"PBO:0078484"}


id: PBO:0043402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytidine/uridine monophosphate kinase 2","termid":"PBO:0043402"}


id: PBO:0058395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4767","termid":"PBO:0058395"}


id: PBO:0046502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERI1 exoribonuclease family member 3","termid":"PBO:0046502"}


id: PBO:0071970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS6KB2 antisense RNA 1","termid":"PBO:0071970"}


id: PBO:0079980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP9Y pseudogene 18","termid":"PBO:0079980"}


id: PBO:0079254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetratricopeptide repeat domain 24","termid":"PBO:0079254"}


id: PBO:0047338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibulin 7","termid":"PBO:0047338"}


id: PBO:0073927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 16 member 14 pseudogene 1","termid":"PBO:0073927"}


id: PBO:0071099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 101","termid":"PBO:0071099"}


id: GO:0060071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A type of non-canonical Wnt signaling pathway in which Wnt binding to its receptor on the surface of a target cell results in the activation small G proteins such as Rho, Rac, and Cdc42 which, in turn activate effectors, including C-Jun N-terminal kinase (JNK) and Rho kinase (Rok). The signaling ends with change in the transcription of target genes and/or reorganisation of the cytoskeleton.","definition_xrefs":["PMID:37804416","PMID:11532397","PMID:28293032","PMID:25349257"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-canonical Wnt signaling pathway","termid":"GO:0035567"}],"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":"Wnt signaling pathway, planar cell polarity pathway","secondary_identifiers":["Reactome:R-HSA-4086400"],"synonyms":[{"name":"PCP pathway","type":"exact"},{"name":"Wnt receptor signaling pathway, planar cell polarity pathway","type":"exact"},{"name":"Wnt receptor signalling pathway, planar cell polarity pathway","type":"exact"},{"name":"Wnt-JNK signaling pathway","type":"related"},{"name":"Wnt-PCP signaling pathway","type":"related"},{"name":"Wnt-activated signaling pathway, planar cell polarity pathway","type":"exact"},{"name":"non-canonical Wnt signaling pathway","type":"related"},{"name":"planar cell polarity pathway","type":"exact"}],"termid":"GO:0060071"}


id: MONDO:0009006
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Complement component 2 deficiency (C2D) is a genetic condition that affects the immune system. Signs and symptoms include recurrent bacterial infections and risk for a variety of autoimmune conditions. Infections can be very serious and are common in early life. They become less frequent during the teen and adult years. The most frequent autoimmune conditions associated with C2D are lupus (10-20%) and vasculitis. C2D is caused by mutations in the C2 gene and is inherited in an autosomal recessive fashion.","direct_ancestors":[{"relation_name":"is_a","term_name":"classic complement early component deficiency","termid":"MONDO:0000015"},{"relation_name":"is_a","term_name":"immunodeficiency due to a classical component pathway complement deficiency","termid":"MONDO:0015699"}],"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":"complement component 2 deficiency","secondary_identifiers":["UMLS:C3150275","NCIT:C119992","DOID:0060295","NANDO:2200781","OMIM:217000","GARD:1452","MEDGEN:461625"],"synonyms":[{"name":"C2 complement deficiency","type":"exact"},{"name":"C2 deficiency","type":"related"},{"name":"C2D","type":"related"},{"name":"complement component 2 deficiency","type":"exact"},{"name":"complement deficiency caused by mutation in C2","type":"exact"}],"termid":"MONDO:0009006","xrefs":{"Monarch":{"xref_id":"0009006"}}}


id: PBO:0056684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maternally expressed 8, small nucleolar RNA host gene","termid":"PBO:0056684"}


id: MONDO:0002906
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete scleroderma (obsolete MONDO:0002906)","termid":"MONDO:0002906","xrefs":{"Monarch":{"xref_id":"0002906"}}}


id: GO:0033036
data:
  {"annotated_genes":["SJAG_02264","SJAG_04656","SJAG_00794","SJAG_04978","SJAG_04931","SJAG_00632","SJAG_04021","SJAG_03864","SJAG_03246","SJAG_05184","SJAG_04347","SJAG_05302","SJAG_02117","SJAG_02456","SJAG_03540","SJAG_04598","SJAG_02437","SJAG_01655","SJAG_02524","SJAG_03172","SJAG_00299","SJAG_01496","SJAG_03156","SJAG_04051","SJAG_02277","SJAG_00586","SJAG_01025","SJAG_04024","SJAG_03721","SJAG_00589","SJAG_01467","SJAG_03690","SJAG_04930","SJAG_04158","SJAG_03250","SJAG_03933","SJAG_00375","SJAG_02422","SJAG_01772","SJAG_00753","SJAG_02208","SJAG_00143","SJAG_01017","SJAG_00192","SJAG_01083","SJAG_04343","SJAG_03683","SJAG_04517","SJAG_05030","SJAG_04366","SJAG_00208","SJAG_04336","SJAG_00333","SJAG_04400","SJAG_03774","SJAG_03515","SJAG_00907","SJAG_03437","SJAG_00821","SJAG_01071","SJAG_00850","SJAG_02640","SJAG_04312","SJAG_02034","SJAG_03158","SJAG_02354","SJAG_02371","SJAG_05209","SJAG_01470","SJAG_04565","SJAG_02797","SJAG_01223","SJAG_03048","SJAG_00840","SJAG_01135","SJAG_05220","SJAG_01652","SJAG_03404","SJAG_03560","SJAG_02586","SJAG_02349","SJAG_03440","SJAG_04349","SJAG_01584","SJAG_00093","SJAG_05345","SJAG_02375","SJAG_01224","SJAG_00383","SJAG_05013","SJAG_03002","SJAG_00360","SJAG_00175","SJAG_04411","SJAG_03126","SJAG_03693","SJAG_01945","SJAG_00032","SJAG_01633","SJAG_01360","SJAG_01775","SJAG_03504","SJAG_02368","SJAG_04489","SJAG_01211","SJAG_02736","SJAG_04643","SJAG_02210","SJAG_02750","SJAG_02323","SJAG_00800","SJAG_00330","SJAG_04472","SJAG_03810","SJAG_04379","SJAG_01358","SJAG_03963","SJAG_02160","SJAG_04734","SJAG_02914","SJAG_01297","SJAG_01925","SJAG_00826","SJAG_00430","SJAG_01281","SJAG_01560","SJAG_01626","SJAG_02624","SJAG_02077","SJAG_03892","SJAG_02114","SJAG_00181","SJAG_00578","SJAG_01095","SJAG_01114","SJAG_02425","SJAG_00641","SJAG_03011","SJAG_01371","SJAG_00404","SJAG_02655","SJAG_00820","SJAG_04966","SJAG_01917","SJAG_03396","SJAG_04645","SJAG_01013","SJAG_02355","SJAG_04464","SJAG_03502","SJAG_03467","SJAG_04837","SJAG_02805","SJAG_01684","SJAG_03345","SJAG_01442","SJAG_05950","SJAG_00661","SJAG_01809","SJAG_02588","SJAG_03315","SJAG_03299","SJAG_02583","SJAG_02661","SJAG_01805","SJAG_03270","SJAG_04622","SJAG_03726","SJAG_00416","SJAG_05266","SJAG_00176","SJAG_00355","SJAG_01329","SJAG_02228","SJAG_03684","SJAG_04275","SJAG_01445","SJAG_04358","SJAG_00918","SJAG_01178","SJAG_05315","SJAG_02282","SJAG_05344","SJAG_04956","SJAG_01039","SJAG_00216","SJAG_02209","SJAG_04901","SJAG_03783","SJAG_04886","SJAG_04739","SJAG_00587","SJAG_01715","SJAG_00530","SJAG_00357","SJAG_00054","SJAG_01516","SJAG_01225","SJAG_02453","SJAG_04129","SJAG_00373","SJAG_02004","SJAG_03781","SJAG_02572","SJAG_03741","SJAG_02539","SJAG_03643","SJAG_03499","SJAG_04148","SJAG_04960","SJAG_02814","SJAG_01529","SJAG_04432","SJAG_03848","SJAG_00471","SJAG_04014","SJAG_01597","SJAG_04684","SJAG_01780","SJAG_01686","SJAG_01488","SJAG_05210","SJAG_00204","SJAG_04434","SJAG_01415","SJAG_01456","SJAG_02132","SJAG_02234","SJAG_00576","SJAG_04902","SJAG_01782","SJAG_01374","SJAG_01949","SJAG_00596","SJAG_01613","SJAG_01116","SJAG_03415","SJAG_03847","SJAG_04721","SJAG_03283","SJAG_04763","SJAG_00803","SJAG_02045","SJAG_01001","SJAG_02529","SJAG_01722","SJAG_01909","SJAG_04474","SJAG_05319","SJAG_02520","SJAG_04996","SJAG_00564","SJAG_02511","SJAG_00380","SJAG_04740","SJAG_01196","SJAG_00919","SJAG_03710","SJAG_01282","SJAG_04126","SJAG_01459","SJAG_03358","SJAG_01951","SJAG_01245","SJAG_00916","SJAG_00072","SJAG_03662","SJAG_05414","SJAG_02022","SJAG_04609","SJAG_03970","SJAG_04428","SJAG_01027","SJAG_02592","SJAG_00104","SJAG_00603","SJAG_04208","SJAG_00702","SJAG_00645","SJAG_02584","SJAG_01640","SJAG_00102","SJAG_05196","SJAG_04083","SJAG_03746","SJAG_03552","SJAG_00196","SJAG_01748","SJAG_03137","SJAG_01981","SJAG_00368","SJAG_01127","SJAG_02731","SJAG_01879","SJAG_01697","SJAG_00669","SJAG_03718","SJAG_04600","SJAG_01449","SJAG_02757","SJAG_02516","SJAG_04857","SJAG_16459","SJAG_02943","SJAG_01527","SJAG_04294","SJAG_03153","SJAG_01508","SJAG_03976","SJAG_01382","SJAG_02299","SJAG_03338","SJAG_02274","SJAG_04629","SJAG_00687","SJAG_02534","SJAG_00137","SJAG_01731","SJAG_05194","SJAG_04912","SJAG_00891","SJAG_00326","SJAG_01615","SJAG_00557","SJAG_03633","SJAG_02645","SJAG_04592","SJAG_03005","SJAG_02957","SJAG_00277","SJAG_02241","SJAG_01165","SJAG_02619","SJAG_02336","SJAG_03453","SJAG_01065","SJAG_01030","SJAG_03889","SJAG_01328","SJAG_00858","SJAG_00178","SJAG_02811","SJAG_05207","SJAG_03324","SJAG_01940","SJAG_00959","SJAG_04597","SJAG_04023","SJAG_00108","SJAG_01305","SJAG_01999","SJAG_00261","SJAG_04589","SJAG_00490","SJAG_03050","SJAG_04017","SJAG_04552","SJAG_03838","SJAG_00171","SJAG_02761","SJAG_00279","SJAG_02998","SJAG_03536","SJAG_03072","SJAG_00804","SJAG_04509","SJAG_00230","SJAG_00065","SJAG_04480","SJAG_01647","SJAG_00064","SJAG_03209","SJAG_03029","SJAG_00992","SJAG_03729","SJAG_02693","SJAG_01437","SJAG_02789","SJAG_02211","SJAG_03385","SJAG_01834","SJAG_03416","SJAG_04413","SJAG_00727","SJAG_01586","SJAG_03300","SJAG_03044","SJAG_01546","SJAG_04070","SJAG_06440","SJAG_01324","SJAG_00569","SJAG_01534","SJAG_02997","SJAG_00379","SJAG_04202","SJAG_03860","SJAG_04391","SJAG_00018","SJAG_04112","SJAG_04536","SJAG_02330","SJAG_02418","SJAG_04076","SJAG_01373","SJAG_03054","SJAG_03836","SJAG_00298","SJAG_04360","SJAG_02065","SJAG_03915","SJAG_02320","SJAG_04402","SJAG_01229","SJAG_05268","SJAG_04703","SJAG_01621","SJAG_00144","SJAG_04984","SJAG_02581","SJAG_04002","SJAG_02525","SJAG_02103","SJAG_03756","SJAG_01120","SJAG_03470","SJAG_05328","SJAG_00906","SJAG_03930","SJAG_04259","SJAG_03244","SJAG_03986","SJAG_01405","SJAG_01642","SJAG_01409","SJAG_01759","SJAG_02912","SJAG_02392","SJAG_02824","SJAG_04461","SJAG_01379","SJAG_02704","SJAG_01242","SJAG_01590","SJAG_02737","SJAG_04218","SJAG_03865","SJAG_03347","SJAG_04513","SJAG_00968","SJAG_03327","SJAG_04569","SJAG_01558","SJAG_01240","SJAG_01598","SJAG_00405","SJAG_04936","SJAG_03593","SJAG_03851","SJAG_00284","SJAG_01084","SJAG_01367","SJAG_01407","SJAG_01738","SJAG_02839","SJAG_01185","SJAG_03247","SJAG_03959","SJAG_00971","SJAG_04196","SJAG_04310","SJAG_04466","SJAG_00938","SJAG_02897","SJAG_04909","SJAG_05259","SJAG_01745","SJAG_00332","SJAG_05300","SJAG_00314","SJAG_02695","SJAG_04370","SJAG_02204","SJAG_01167","SJAG_01311","SJAG_00851","SJAG_01088","SJAG_02482","SJAG_04044","SJAG_04947","SJAG_03907","SJAG_04923","SJAG_04115","SJAG_00900","SJAG_05303","SJAG_00899","SJAG_02315","SJAG_03602","SJAG_01789","SJAG_02361"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60480,63674,70233],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140331"},{"annotations":[76511],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0015917"},{"annotations":[113811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098653"},{"annotations":[93154,111809,91408,118806,104639],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072766"},{"annotations":[115164,116308,70912,64512,89937,93315,107583,89824,65861,64926,69296,93454],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0120113"},{"annotations":[89805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120207"},{"annotations":[61966,114860,120765,96713,93104,102947,67803,114643],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0099638"},{"annotations":[111466,119376,74503,75479,75943,75044],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035621"},{"annotations":[96236,78798],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034203"},{"annotations":[108246,96966,71926,79334,110637,114862,108875,111426],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043001"},{"annotations":[57469],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120009"},{"annotations":[109356,118101,110489,105862,109481,107675,91043,99301,100442,99367,108573,111371,92713,103098,102345],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120010"},{"annotations":[96055,110043,111209,108159,113182,118079,93295,104432],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120011"},{"annotations":[114542,100918,78687,115327,64952,64331,99119,92982,59070,65606,111023,64216,97332,101723,100726,104514,95676,106797,73712,79262,90438,111343,113867,114021,116989,64554,64486,92382,81422,59327,71017,75379,102900,93346,72607,80555,115487,99908,107856,116015,118694,120718,96762,58649,98120,99558,74009,108961,114312,61008,105556,96967,109329,76239,80743,70544,91534,96201,58900,101328,102669,112597,106433,59113,69524,95707,70765,63301,58253,109391,81691,95044,109223,67326,72240,104960,118233,68873,95310,79589,95856,97908,119414,94958,66927,100858,106729,118758,73693,111499,96811,66137,79765,97431,97871,93289,110261,68671,90479,99577,71525,101579,109865,101531,68346,69773,95448,68574,111673,116736,80280,69927,72190,117087,70607,101840,116228,107981,77911,97597,118832,81759,58665,77054,109141,77535,98695,69919,107016,98691,73701,93446,78220,63832,105546,96088,120898,89870,92961,90967,118284,100267,114045,104352,103739,96617,104129,111427],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006886"},{"annotations":[63023,73684,78741],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032366"},{"annotations":[102061],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0170046"},{"annotations":[104742,118791],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140043"},{"annotations":[68198],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032065"},{"annotations":[101996,95833,112713],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097248"},{"annotations":[117784,95609,70177,102198,66730,104255,97129,110983,101034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990571"},{"annotations":[100302,98944],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160203"},{"annotations":[81939,74454,79250,91301,102969,78422,61701,63276,75816,74538,119127],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006406"},{"annotations":[74922],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031990"},{"annotations":[58699,60138,65570],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051028"},{"annotations":[89903],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0042997"},{"annotations":[107638],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0042308"},{"annotations":[92774,97669],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903067"},{"annotations":[96221],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140325"},{"annotations":[116330],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1900181"},{"annotations":[97670],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903077"},{"annotations":[77809,78693,102970,76727,74923,75404],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006607"},{"annotations":[73807,103100,92333,92331,104032,92328,111357,76520,92336,74699,92329,74792,76276,92332,92335,92330,101286,92334],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045332"},{"annotations":[74973],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0017121"},{"annotations":[103682,74921,74768,104471,109468,111704,120806,76201,94006,119887,112275,75492,76447,112974,113602,79066,103216,73128,117661,117913,118171,77421,98347,76107,82163,98759,71631,75876,105762,116318],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016973"},{"annotations":[102258,112865,95619,103670],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0046827"},{"annotations":[92660,96184,104205],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0042307"},{"annotations":[100242],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0120047"},{"annotations":[81991,99145,99861,74905,110150],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031204"},{"annotations":[74750],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0032527"},{"annotations":[65612,65972,119888,73315,94981,102971,111434,119538,119254],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006611"},{"annotations":[79441,78819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045041"},{"annotations":[109346,111723,102137,119113,104515,101055,113651,92706,91356,109400,109423,107017,90145,96331,101239,105103,101355,108003,117088,98696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030150"},{"annotations":[81427,73256,74751,71744,95800,78068,80236,96095,97941,73044,108167,117662,74539,81828,99640,90725,77422,74351,72740,73314,67503,82164,75466,79660,75493,60872,74598,72141,76202,77326,106890,75746,81940,76881,77415,75964],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006606"},{"annotations":[81410,98288,75060,104080,72395,71882,73790,113244],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0016558"},{"annotations":[72420,63446,75452],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0016560"},{"annotations":[119172,65297,117159,100384],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016562"},{"annotations":[97244,92238,113245],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0045046"},{"annotations":[100173,106304,110151,111184,114108,115697,103010,93485,99862,69308,106612,110238,107998,112249,100405,116251,96649,105330],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045048"},{"annotations":[58495,118126,75719,104745,75175,109424,90470,79524,77448],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[76218,58620,80289,80031,80350],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032979"},{"annotations":[78347,100394,112246,59123,113645,111893,100043,71687,109401],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0045040"},{"annotations":[108996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044379"},{"annotations":[93108,115904,118039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990896"},{"annotations":[97474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072741"},{"annotations":[98790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904518"},{"annotations":[72710,79937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070973"},{"annotations":[67609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034067"},{"annotations":[79726,60017,77120],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034501"},{"annotations":[106356,101912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903360"},{"annotations":[92951,107185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071574"},{"annotations":[98684,93109,115789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902441"},{"annotations":[73677,79197,79879],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072657"},{"annotations":[72455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035372"},{"annotations":[120521,94139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904498"},{"annotations":[78691,76878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036228"},{"annotations":[91346,97532,103222,92363,116814,92661,66755,69857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072659"},{"annotations":[93946],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006621"},{"annotations":[92815],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0044395"},{"annotations":[75731,82126,98364,79909,78932,72974,79033,77476,74485,79457],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006623"},{"annotations":[67851,57233,61838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071806"},{"annotations":[77544,66166,81840,61828,74856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015031"},{"annotations":[105566],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0099117"},{"annotations":[105722,120546,102204,110105],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0140210"},{"annotations":[91563,98587,118778,115955,90957,92793,110728,102341,100438,109341,111738],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1990976"},{"annotations":[118040,109974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904601"},{"annotations":[75242,102710,73901,72834,93318,97780,108395,80216,72664,111220,73865,89771,79945,89940,79483,93457,116567,99771,75263],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0043328"},{"annotations":[89716,93836],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0033157"},{"annotations":[109793],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905391"},{"annotations":[80851,77353],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0030970"},{"annotations":[81827,95802,97943,106892,76880,77325],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006405"},{"annotations":[104377],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006404"},{"annotations":[110152,74957,77296,75366,99863,104404],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006616"},{"annotations":[74549,76806,115987,89738,116954],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071816"},{"annotations":[107105,107576,73895,80310],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006409"},{"annotations":[80895],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016031"},{"annotations":[81292],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071528"},{"annotations":[120747,107546,94020,74774,112880,80265,80934,80974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070086"}]},"cv_name":"biological_process","definition":"Any process in which a macromolecule is transported to, or maintained in, a specific location.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localization","termid":"GO:0051179"}],"gene_count":500,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00032":null,"SJAG_00054":null,"SJAG_00064":null,"SJAG_00065":null,"SJAG_00072":null,"SJAG_00093":null,"SJAG_00102":null,"SJAG_00104":null,"SJAG_00108":null,"SJAG_00137":null,"SJAG_00143":null,"SJAG_00144":null,"SJAG_00171":null,"SJAG_00175":null,"SJAG_00176":null,"SJAG_00178":null,"SJAG_00181":null,"SJAG_00192":null,"SJAG_00196":null,"SJAG_00204":null,"SJAG_00208":null,"SJAG_00216":null,"SJAG_00230":null,"SJAG_00261":null,"SJAG_00277":null,"SJAG_00279":null,"SJAG_00284":null,"SJAG_00298":null,"SJAG_00299":null,"SJAG_00314":null,"SJAG_00326":null,"SJAG_00330":null,"SJAG_00332":null,"SJAG_00333":null,"SJAG_00355":null,"SJAG_00357":null,"SJAG_00360":null,"SJAG_00368":null,"SJAG_00373":null,"SJAG_00375":null,"SJAG_00379":null,"SJAG_00380":null,"SJAG_00383":null,"SJAG_00404":null,"SJAG_00405":null,"SJAG_00416":null,"SJAG_00430":null,"SJAG_00471":null,"SJAG_00490":null,"SJAG_00530":null,"SJAG_00557":null,"SJAG_00564":null,"SJAG_00569":null,"SJAG_00576":null,"SJAG_00578":null,"SJAG_00586":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00596":null,"SJAG_00603":null,"SJAG_00632":null,"SJAG_00641":null,"SJAG_00645":null,"SJAG_00661":null,"SJAG_00669":null,"SJAG_00687":null,"SJAG_00702":null,"SJAG_00727":null,"SJAG_00753":null,"SJAG_00794":null,"SJAG_00800":null,"SJAG_00803":null,"SJAG_00804":null,"SJAG_00820":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00840":null,"SJAG_00850":null,"SJAG_00851":null,"SJAG_00858":null,"SJAG_00891":null,"SJAG_00899":null,"SJAG_00900":null,"SJAG_00906":null,"SJAG_00907":null,"SJAG_00916":null,"SJAG_00918":null,"SJAG_00919":null,"SJAG_00938":null,"SJAG_00959":null,"SJAG_00968":null,"SJAG_00971":null,"SJAG_00992":null,"SJAG_01001":null,"SJAG_01013":null,"SJAG_01017":null,"SJAG_01025":null,"SJAG_01027":null,"SJAG_01030":null,"SJAG_01039":null,"SJAG_01065":null,"SJAG_01071":null,"SJAG_01083":null,"SJAG_01084":null,"SJAG_01088":null,"SJAG_01095":null,"SJAG_01114":null,"SJAG_01116":null,"SJAG_01120":null,"SJAG_01127":null,"SJAG_01135":null,"SJAG_01165":null,"SJAG_01167":null,"SJAG_01178":null,"SJAG_01185":null,"SJAG_01196":null,"SJAG_01211":null,"SJAG_01223":null,"SJAG_01224":null,"SJAG_01225":null,"SJAG_01229":null,"SJAG_01240":null,"SJAG_01242":null,"SJAG_01245":null,"SJAG_01281":null,"SJAG_01282":null,"SJAG_01297":null,"SJAG_01305":null,"SJAG_01311":null,"SJAG_01324":null,"SJAG_01328":null,"SJAG_01329":null,"SJAG_01358":null,"SJAG_01360":null,"SJAG_01367":null,"SJAG_01371":null,"SJAG_01373":null,"SJAG_01374":null,"SJAG_01379":null,"SJAG_01382":null,"SJAG_01405":null,"SJAG_01407":null,"SJAG_01409":null,"SJAG_01415":null,"SJAG_01437":null,"SJAG_01442":null,"SJAG_01445":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01459":null,"SJAG_01467":null,"SJAG_01470":null,"SJAG_01488":null,"SJAG_01496":null,"SJAG_01508":null,"SJAG_01516":null,"SJAG_01527":null,"SJAG_01529":null,"SJAG_01534":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01560":null,"SJAG_01584":null,"SJAG_01586":null,"SJAG_01590":null,"SJAG_01597":null,"SJAG_01598":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01621":null,"SJAG_01626":null,"SJAG_01633":null,"SJAG_01640":null,"SJAG_01642":null,"SJAG_01647":null,"SJAG_01652":null,"SJAG_01655":null,"SJAG_01684":null,"SJAG_01686":null,"SJAG_01697":null,"SJAG_01715":null,"SJAG_01722":null,"SJAG_01731":null,"SJAG_01738":null,"SJAG_01745":null,"SJAG_01748":null,"SJAG_01759":null,"SJAG_01772":null,"SJAG_01775":null,"SJAG_01780":null,"SJAG_01782":null,"SJAG_01789":null,"SJAG_01805":null,"SJAG_01809":null,"SJAG_01834":null,"SJAG_01879":null,"SJAG_01909":null,"SJAG_01917":null,"SJAG_01925":null,"SJAG_01940":null,"SJAG_01945":null,"SJAG_01949":null,"SJAG_01951":null,"SJAG_01981":null,"SJAG_01999":null,"SJAG_02004":null,"SJAG_02022":null,"SJAG_02034":null,"SJAG_02045":null,"SJAG_02065":null,"SJAG_02077":null,"SJAG_02103":null,"SJAG_02114":null,"SJAG_02117":null,"SJAG_02132":null,"SJAG_02160":null,"SJAG_02204":null,"SJAG_02208":null,"SJAG_02209":null,"SJAG_02210":null,"SJAG_02211":null,"SJAG_02228":null,"SJAG_02234":null,"SJAG_02241":null,"SJAG_02264":null,"SJAG_02274":null,"SJAG_02277":null,"SJAG_02282":null,"SJAG_02299":null,"SJAG_02315":null,"SJAG_02320":null,"SJAG_02323":null,"SJAG_02330":null,"SJAG_02336":null,"SJAG_02349":null,"SJAG_02354":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_02368":null,"SJAG_02371":null,"SJAG_02375":null,"SJAG_02392":null,"SJAG_02418":null,"SJAG_02422":null,"SJAG_02425":null,"SJAG_02437":null,"SJAG_02453":null,"SJAG_02456":null,"SJAG_02482":null,"SJAG_02511":null,"SJAG_02516":null,"SJAG_02520":null,"SJAG_02524":null,"SJAG_02525":null,"SJAG_02529":null,"SJAG_02534":null,"SJAG_02539":null,"SJAG_02572":null,"SJAG_02581":null,"SJAG_02583":null,"SJAG_02584":null,"SJAG_02586":null,"SJAG_02588":null,"SJAG_02592":null,"SJAG_02619":null,"SJAG_02624":null,"SJAG_02640":null,"SJAG_02645":null,"SJAG_02655":null,"SJAG_02661":null,"SJAG_02693":null,"SJAG_02695":null,"SJAG_02704":null,"SJAG_02731":null,"SJAG_02736":null,"SJAG_02737":null,"SJAG_02750":null,"SJAG_02757":null,"SJAG_02761":null,"SJAG_02789":null,"SJAG_02797":null,"SJAG_02805":null,"SJAG_02811":null,"SJAG_02814":null,"SJAG_02824":null,"SJAG_02839":null,"SJAG_02897":null,"SJAG_02912":null,"SJAG_02914":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_02997":null,"SJAG_02998":null,"SJAG_03002":null,"SJAG_03005":null,"SJAG_03011":null,"SJAG_03029":null,"SJAG_03044":null,"SJAG_03048":null,"SJAG_03050":null,"SJAG_03054":null,"SJAG_03072":null,"SJAG_03126":null,"SJAG_03137":null,"SJAG_03153":null,"SJAG_03156":null,"SJAG_03158":null,"SJAG_03172":null,"SJAG_03209":null,"SJAG_03244":null,"SJAG_03246":null,"SJAG_03247":null,"SJAG_03250":null,"SJAG_03270":null,"SJAG_03283":null,"SJAG_03299":null,"SJAG_03300":null,"SJAG_03315":null,"SJAG_03324":null,"SJAG_03327":null,"SJAG_03338":null,"SJAG_03345":null,"SJAG_03347":null,"SJAG_03358":null,"SJAG_03385":null,"SJAG_03396":null,"SJAG_03404":null,"SJAG_03415":null,"SJAG_03416":null,"SJAG_03437":null,"SJAG_03440":null,"SJAG_03453":null,"SJAG_03467":null,"SJAG_03470":null,"SJAG_03499":null,"SJAG_03502":null,"SJAG_03504":null,"SJAG_03515":null,"SJAG_03536":null,"SJAG_03540":null,"SJAG_03552":null,"SJAG_03560":null,"SJAG_03593":null,"SJAG_03602":null,"SJAG_03633":null,"SJAG_03643":null,"SJAG_03662":null,"SJAG_03683":null,"SJAG_03684":null,"SJAG_03690":null,"SJAG_03693":null,"SJAG_03710":null,"SJAG_03718":null,"SJAG_03721":null,"SJAG_03726":null,"SJAG_03729":null,"SJAG_03741":null,"SJAG_03746":null,"SJAG_03756":null,"SJAG_03774":null,"SJAG_03781":null,"SJAG_03783":null,"SJAG_03810":null,"SJAG_03836":null,"SJAG_03838":null,"SJAG_03847":null,"SJAG_03848":null,"SJAG_03851":null,"SJAG_03860":null,"SJAG_03864":null,"SJAG_03865":null,"SJAG_03889":null,"SJAG_03892":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03930":null,"SJAG_03933":null,"SJAG_03959":null,"SJAG_03963":null,"SJAG_03970":null,"SJAG_03976":null,"SJAG_03986":null,"SJAG_04002":null,"SJAG_04014":null,"SJAG_04017":null,"SJAG_04021":null,"SJAG_04023":null,"SJAG_04024":null,"SJAG_04044":null,"SJAG_04051":null,"SJAG_04070":null,"SJAG_04076":null,"SJAG_04083":null,"SJAG_04112":null,"SJAG_04115":null,"SJAG_04126":null,"SJAG_04129":null,"SJAG_04148":null,"SJAG_04158":null,"SJAG_04196":null,"SJAG_04202":null,"SJAG_04208":null,"SJAG_04218":null,"SJAG_04259":null,"SJAG_04275":null,"SJAG_04294":null,"SJAG_04310":null,"SJAG_04312":null,"SJAG_04336":null,"SJAG_04343":null,"SJAG_04347":null,"SJAG_04349":null,"SJAG_04358":null,"SJAG_04360":null,"SJAG_04366":null,"SJAG_04370":null,"SJAG_04379":null,"SJAG_04391":null,"SJAG_04400":null,"SJAG_04402":null,"SJAG_04411":null,"SJAG_04413":null,"SJAG_04428":null,"SJAG_04432":null,"SJAG_04434":null,"SJAG_04461":null,"SJAG_04464":null,"SJAG_04466":null,"SJAG_04472":null,"SJAG_04474":null,"SJAG_04480":null,"SJAG_04489":null,"SJAG_04509":null,"SJAG_04513":null,"SJAG_04517":null,"SJAG_04536":null,"SJAG_04552":null,"SJAG_04565":null,"SJAG_04569":null,"SJAG_04589":null,"SJAG_04592":null,"SJAG_04597":null,"SJAG_04598":null,"SJAG_04600":null,"SJAG_04609":null,"SJAG_04622":null,"SJAG_04629":null,"SJAG_04643":null,"SJAG_04645":null,"SJAG_04656":null,"SJAG_04684":null,"SJAG_04703":null,"SJAG_04721":null,"SJAG_04734":null,"SJAG_04739":null,"SJAG_04740":null,"SJAG_04763":null,"SJAG_04837":null,"SJAG_04857":null,"SJAG_04886":null,"SJAG_04901":null,"SJAG_04902":null,"SJAG_04909":null,"SJAG_04912":null,"SJAG_04923":null,"SJAG_04930":null,"SJAG_04931":null,"SJAG_04936":null,"SJAG_04947":null,"SJAG_04956":null,"SJAG_04960":null,"SJAG_04966":null,"SJAG_04978":null,"SJAG_04984":null,"SJAG_04996":null,"SJAG_05013":null,"SJAG_05030":null,"SJAG_05184":null,"SJAG_05194":null,"SJAG_05196":null,"SJAG_05207":null,"SJAG_05209":null,"SJAG_05210":null,"SJAG_05220":null,"SJAG_05259":null,"SJAG_05266":null,"SJAG_05268":null,"SJAG_05300":null,"SJAG_05302":null,"SJAG_05303":null,"SJAG_05315":null,"SJAG_05319":null,"SJAG_05328":null,"SJAG_05344":null,"SJAG_05345":null,"SJAG_05414":null,"SJAG_05950":null,"SJAG_06440":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"macromolecule localization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"synonyms":[{"name":"macromolecule localisation","type":"exact"}],"termid":"GO:0033036","terms_by_termid":{"GO:0006404":null,"GO:0006405":null,"GO:0006406":null,"GO:0006409":null,"GO:0006606":null,"GO:0006607":null,"GO:0006611":null,"GO:0006616":null,"GO:0006621":null,"GO:0006623":null,"GO:0006886":null,"GO:0015031":null,"GO:0015917":null,"GO:0016031":null,"GO:0016558":null,"GO:0016560":null,"GO:0016562":null,"GO:0016973":null,"GO:0017121":null,"GO:0030150":null,"GO:0030970":null,"GO:0031204":null,"GO:0031990":null,"GO:0032065":null,"GO:0032366":null,"GO:0032527":null,"GO:0032979":null,"GO:0033157":null,"GO:0034067":null,"GO:0034203":null,"GO:0034501":null,"GO:0035372":null,"GO:0035621":null,"GO:0036228":null,"GO:0042307":null,"GO:0042308":null,"GO:0042997":null,"GO:0043001":null,"GO:0043328":null,"GO:0044379":null,"GO:0044395":null,"GO:0045039":null,"GO:0045040":null,"GO:0045041":null,"GO:0045046":null,"GO:0045048":null,"GO:0045332":null,"GO:0046827":null,"GO:0051028":null,"GO:0070086":null,"GO:0070973":null,"GO:0071528":null,"GO:0071574":null,"GO:0071806":null,"GO:0071816":null,"GO:0072657":null,"GO:0072659":null,"GO:0072741":null,"GO:0072766":null,"GO:0097248":null,"GO:0098653":null,"GO:0099117":null,"GO:0099638":null,"GO:0120009":null,"GO:0120010":null,"GO:0120011":null,"GO:0120047":null,"GO:0120113":null,"GO:0120207":null,"GO:0140043":null,"GO:0140210":null,"GO:0140325":null,"GO:0140331":null,"GO:0160203":null,"GO:0170046":null,"GO:1900181":null,"GO:1902441":null,"GO:1903067":null,"GO:1903077":null,"GO:1903360":null,"GO:1904498":null,"GO:1904518":null,"GO:1904601":null,"GO:1905391":null,"GO:1990571":null,"GO:1990896":null,"GO:1990976":null}}


id: GO:0070885
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the calcineurin-NFAT signaling cascade.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of calcineurin-NFAT signaling cascade","termid":"GO:0070884"},{"relation_name":"is_a","term_name":"negative regulation of calcineurin-mediated signaling","termid":"GO:0106057"},{"relation_name":"negatively_regulates","term_name":"calcineurin-NFAT signaling cascade","termid":"GO:0033173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of calcineurin-NFAT signaling cascade","secondary_identifiers":["GO:0051534"],"synonyms":[{"name":"down regulation of calcineurin-NFAT signaling cascade","type":"exact"},{"name":"down-regulation of calcineurin-NFAT signaling cascade","type":"exact"},{"name":"downregulation of calcineurin-NFAT signaling cascade","type":"exact"},{"name":"inhibition of NFAT protein import into nucleus","type":"narrow"},{"name":"inhibition of calcineurin-NFAT signaling cascade","type":"narrow"},{"name":"negative regulation of NFAT protein import into nucleus","type":"narrow"},{"name":"negative regulation of calcineurin-NFAT signaling pathway","type":"related"},{"name":"negative regulation of calcineurin-NFAT signalling cascade","type":"exact"},{"name":"termination of calcineurin-NFAT signaling cascade","type":"narrow"}],"termid":"GO:0070885"}


id: PBO:0042098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC169-SOHLH2 readthrough","termid":"PBO:0042098"}


id: PBO:0078375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triggering receptor expressed on myeloid cells 1","termid":"PBO:0078375"}


id: PBO:0028368
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_GT_microsatellite_DNA_binding","termid":"PBO:0028368"}


id: GO:0045499
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Providing the environmental signal that initiates the directed movement of a motile cell or organism towards a lower concentration of that signal.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor ligand activity","termid":"GO:0048018"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0098772","GO:0140677","GO:0003674"],"is_obsolete":false,"name":"chemorepellent activity","synonyms":[{"name":"chemorepellant activity","type":"exact"}],"termid":"GO:0045499"}


id: PBO:0052654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 22","termid":"PBO:0052654"}


id: PBO:0043741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 7A2","termid":"PBO:0043741"}


id: PBO:0003524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk31 (predicted)","termid":"PBO:0003524"}


id: GO:1904849
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell chemotaxis to fibroblast growth factor.","definition_xrefs":["GOC:TermGenie","GOC:BHF_miRNA","GO_REF:0000058","GOC:BHF","GOC:rph","PMID:23233752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell migration","termid":"GO:0030335"},{"relation_name":"is_a","term_name":"positive regulation of chemotaxis","termid":"GO:0050921"},{"relation_name":"is_a","term_name":"regulation of cell chemotaxis to fibroblast growth factor","termid":"GO:1904847"},{"relation_name":"positively_regulates","term_name":"cell chemotaxis to fibroblast growth factor","termid":"GO:0035766"}],"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 cell chemotaxis to fibroblast growth factor","synonyms":[{"name":"activation of cell chemotaxis to fibroblast growth factor","type":"narrow"},{"name":"up regulation of cell chemotaxis to fibroblast growth factor","type":"exact"},{"name":"up-regulation of cell chemotaxis to fibroblast growth factor","type":"exact"},{"name":"upregulation of cell chemotaxis to fibroblast growth factor","type":"exact"}],"termid":"GO:1904849"}


id: GO:1900317
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of maltopentaose transport.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of maltopentaose transport","termid":"GO:1900315"},{"relation_name":"is_a","term_name":"positive regulation of pentasaccharide transport","termid":"GO:1900362"},{"relation_name":"positively_regulates","term_name":"maltopentaose transport","termid":"GO:2001101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of maltopentaose transport","synonyms":[{"name":"activation of maltopentaose transport","type":"narrow"},{"name":"up regulation of maltopentaose transport","type":"exact"},{"name":"up-regulation of maltopentaose transport","type":"exact"},{"name":"upregulation of maltopentaose transport","type":"exact"}],"termid":"GO:1900317"}


id: PBO:0074193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 39 member 3","termid":"PBO:0074193"}


id: SO:0000425
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The long terminal repeat found at the five-prime end of the sequence to be inserted into the host genome.","direct_ancestors":[{"relation_name":"is_a","term_name":"long_terminal_repeat","termid":"SO:0000286"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_prime_LTR","synonyms":[{"name":"5' LTR","type":"exact"},{"name":"5' long terminal repeat","type":"exact"},{"name":"five prime LTR","type":"exact"}],"termid":"SO:0000425"}


id: SO:0001729
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 16th residue (a lysine), from the start of the H4 histone protein is acetylated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_4_acetylation_site","termid":"SO:0001972"}],"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":"H4K16_acetylation_site","synonyms":[{"name":"H4K16 acetylation site","type":"exact"},{"name":"H4K16ac","type":"exact"}],"termid":"SO:0001729"}


id: PR:Q9P6N9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A post-GPI attachment to proteins factor 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01083","PANTHER:PTHR13148:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein PER1 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC823.07","secondary_identifiers":["UniProtKB:Q9P6N9"],"synonyms":[{"name":"Spom972h-PGAP3","type":"exact"}],"termid":"PR:Q9P6N9"}


id: PR:O42869
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spa2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42869"],"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 C3G9.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3G9.05","synonyms":[{"name":"Spom972h-spa2","type":"exact"}],"termid":"PR:O42869"}


id: GO:0097471
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A synapse of a mossy fiber onto the dendrite of a granule cell; each mossy fiber can have up to 50 rosettes.","definition_xrefs":["NIF_Subcellular:nlx_subcell_091021","Wikipedia:Mossy_fiber_(cerebellum)"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asymmetric synapse","termid":"GO:0032279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"mossy fiber rosette","synonyms":[{"name":"cerebellar mossy fiber to granule cell synapse","type":"exact"}],"termid":"GO:0097471"}


id: GO:0150195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of substances (e.g. macromolecules, small molecules, ions) through the blood-cerebrospinal fluid barrier.","definition_xrefs":["GOC:bc","PMID:21349151","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular transport","termid":"GO:0010232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"transport across blood-cerebrospinal fluid barrier","synonyms":[{"name":"transport across BCSFB","type":"exact"},{"name":"transport across blood-CSF barrier","type":"exact"},{"name":"transport across blood/CSF barrier","type":"exact"},{"name":"transport across blood/cerebrospinal fluid barrier","type":"exact"}],"termid":"GO:0150195"}


id: MONDO:0013186
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88232],"is_not":false,"summary":null,"term":"MONDO:0013186"}]},"cv_name":"mondo","definition":"Any Noonan syndrome in which the cause of the disease is a mutation in the NRAS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome","termid":"MONDO:0018997"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005046"],"is_obsolete":false,"name":"Noonan syndrome 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C176934","DOID:0060584","GARD:10701","OMIM:613224","UMLS:C2750732","MESH:C548084","MEDGEN:413028"],"synonyms":[{"name":"NRAS Noonan syndrome","type":"exact"},{"name":"NRAS gene related Noonan syndrome","type":"related"},{"name":"NS6","type":"exact"},{"name":"Noonan syndrome 6","type":"exact"},{"name":"Noonan syndrome caused by mutation in NRAS","type":"exact"},{"name":"Noonan syndrome type 6","type":"exact"}],"termid":"MONDO:0013186","terms_by_termid":{"MONDO:0013186":null},"xrefs":{"Monarch":{"xref_id":"0013186"}}}


id: PBO:0033782
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_site-specific_DNA_replication_termination_at_RTS1_barrier","termid":"PBO:0033782"}


id: GO:0102981
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-hydroxy-5-methyl-2-propyl-3(2H)-furanone + NADP = (2E)-4-hydroxy-5-methyl-2-propylidene-3(2H)-furanone + NADPH + H+.","definition_xrefs":["EC:1.3.1.-","GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4-hydroxy-5-methyl-2-propyl-3(2H)-furanone oxidoreductase activity (obsolete GO:0102981)","termid":"GO:0102981"}


id: PBO:0041004
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BLOC-1 related complex subunit 6","termid":"PBO:0041004"}


id: PBO:0084400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lunapark family member involved in ER network formation; regulates the ER asymmetry-induced inheritance block during ER stress; localizes to ER junctions and this localization is regulated by the yeast atlastin ortholog Sey1p; required for reticulophagy where it is proposed to stabilize the actin-dependent remodeling of the ER; interacts with the reticulon protein Rtn1p; induced in response to the DNA-damaging agent MMS","termid":"PBO:0084400"}


id: PBO:0061668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 50 pseudogene 1","termid":"PBO:0061668"}


id: MONDO:0017618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital sucrase-isomaltase deficiency","termid":"MONDO:0009114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"congenital sucrase-isomaltase deficiency with starch intolerance","secondary_identifiers":["Orphanet:306436"],"synonyms":[{"name":"CSID with starch intolerance","type":"exact"},{"name":"congenital sucrase-isomaltose malabsorption with starch intolerance","type":"exact"},{"name":"congenital sucrose intolerance with starch intolerance","type":"exact"},{"name":"disaccharide intolerance with starch intolerance","type":"exact"}],"termid":"MONDO:0017618","xrefs":{"Monarch":{"xref_id":"0017618"}}}


id: MOD:01492
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group.","definition_xrefs":["Unimod:533"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(13)C isotope tagged reagent","termid":"MOD:01428"},{"relation_name":"is_a","term_name":"(15)N isotope tagged reagent","termid":"MOD:01429"},{"relation_name":"is_a","term_name":"(18)O isotope tagged reagent","termid":"MOD:01430"},{"relation_name":"is_a","term_name":"modifications with monoisotopic mass diferences that are nominally equal at 144.099-144.106 Da.","termid":"MOD:01516"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter+balance reagent acylated residue","termid":"MOD:01518"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ4plex-115 reporter+balance reagent acylated residue","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Accurate mass for 115","type":"related"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"iTRAQ115","type":"related"},{"name":"iTRAQ4plex115","type":"related"}],"termid":"MOD:01492"}


id: MONDO:0015979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary immunodeficiency due to a genetic defect in innate immunity (obsolete MONDO:0015135)","termid":"MONDO:0015135"}],"gene_count":0,"genotype_count":0,"name":"obsolete hereditary predisposition to infections (obsolete MONDO:0015979)","secondary_identifiers":["Orphanet:183710"],"synonyms":[{"name":"genetic susceptibility to infections due to particular pathogens","type":"exact"}],"termid":"MONDO:0015979","xrefs":{"Monarch":{"xref_id":"0015979"}}}


id: PBO:0041317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 69 pseudogene 3","termid":"PBO:0041317"}


id: GO:1990665
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterotetrameric protein complex comprising two Annexin A2 (AnxA2) monomers and two copies of its binding partner, S100 protein p11 (S100A10).","definition_xrefs":["PMID:18799458","GOC:BHF","GOC:nc","PMID:23483454","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"AnxA2-p11 complex","synonyms":[{"name":"(A2.p11)2 complex","type":"exact"},{"name":"(p11)2.(AnxA2)2 complex","type":"exact"},{"name":"Annexin A2 tetramer","type":"related"},{"name":"Annexin A2-p11 complex","type":"exact"},{"name":"AnxA2.p11 complex","type":"exact"},{"name":"AnxA2:S100A10 heterotetramer","type":"exact"}],"termid":"GO:1990665"}


id: PBO:0001604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar serine protease Isp6","termid":"PBO:0001604"}


id: PR:O74999
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rhp7 gene.","definition_xrefs":["UniProtKB:O74999","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":"DNA repair protein rhp7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC330.02","synonyms":[{"name":"RAD7 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rhp7","type":"exact"}],"termid":"PR:O74999"}


id: FYPO:0005513
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the kinetochore of a chromosome is increased during one or both meiotic nuclear divisions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to kinetochore during meiosis","termid":"FYPO:0004762"},{"relation_name":"is_a","term_name":"increased protein localization to centromere during meiotic cell cycle","termid":"FYPO:0005598"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"increased protein localization to kinetochore during meiosis","synonyms":[{"name":"increased protein localisation to kinetochore during meiosis","type":"exact"},{"name":"increased protein localization to kinetochore during meiotic nuclear division","type":"exact"},{"name":"increased protein localization to meiotic kinetochore","type":"exact"}],"termid":"FYPO:0005513"}


id: PBO:0110192
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NaTtoU","termid":"PBO:0110192"}


id: GO:0047047
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycerate + CO2 + NAD(P)+ = NAD(P)H + H+ + 2-hydroxy-3-oxosuccinate.","definition_xrefs":["EC:1.1.1.92","MetaCyc:1.1.1.92-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"oxaloglycolate reductase (decarboxylating) activity","synonyms":[{"name":"D-glycerate:NAD(P)+ oxidoreductase (carboxylating)","type":"related"}],"termid":"GO:0047047"}


id: PBO:0091258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LYR family","termid":"PBO:0091258"}


id: PBO:0077675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor superfamily member 25","termid":"PBO:0077675"}


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


id: MONDO:0032728
data:
  {"annotated_genes":["SJAG_01649"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88916],"is_not":false,"summary":null,"term":"MONDO:0032728"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01649":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease, axonal, type 2EE","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5193076","DOID:0111559","MEDGEN:1677426","OMIM:618400"],"synonyms":[{"name":"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2EE","type":"related"},{"name":"CMT2EE","type":"related"},{"name":"Charcot-Marie-Tooth Neuropathy, Type 2Ee","type":"related"}],"termid":"MONDO:0032728","terms_by_termid":{"MONDO:0032728":null},"xrefs":{"Monarch":{"xref_id":"0032728"}}}


id: GO:0062072
data:
  {"annotated_genes":["SJAG_04574","SJAG_03916","SJAG_01601","SJAG_01579"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[93089,100945,105916,112345],"is_not":false,"summary":null,"term":"GO:0062072"}]},"cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H3 trimethylated at lysine 9. In some organisms, there is only H3K9me2, not H3K9me3, but this modification is recognized by homologous readers.","definition_xrefs":["PMID:30110338"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 reader activity","termid":"GO:0140006"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01579":null,"SJAG_01601":null,"SJAG_03916":null,"SJAG_04574":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140566"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0140566","GO:0060090","GO:0030674","GO:0003674"],"is_obsolete":false,"name":"histone H3K9me2/3 reader activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"H3K9me3 modified histone binding","type":"narrow"},{"name":"histone H3K9me2 reader activity","type":"related"},{"name":"histone H3K9me3 reader activity","type":"related"}],"termid":"GO:0062072","terms_by_termid":{"GO:0062072":null}}


id: GO:0033333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a fin over time, from its formation to the mature structure.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"appendage development","termid":"GO:0048736"}],"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":"fin development","termid":"GO:0033333"}


id: PBO:0083985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glutamine synthetase (GS); synthesizes glutamine from glutamate and ammonia; with Glt1p, forms the secondary pathway for glutamate biosynthesis from ammonia; expression regulated by nitrogen source and by amino acid limitation; forms filaments of back-to-back stacks of cylindrical homo-decamers at low pH, leading to enzymatic inactivation and storage during states of advanced cellular starvation; relocalizes from nucleus to cytoplasmic foci upon DNA replication stress","termid":"PBO:0083985"}


id: GO:1905876
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of postsynaptic density organization.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:21887379"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle organization","termid":"GO:0010638"},{"relation_name":"is_a","term_name":"regulation of postsynaptic density organization","termid":"GO:1905874"},{"relation_name":"positively_regulates","term_name":"postsynaptic density organization","termid":"GO:0097106"}],"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 postsynaptic density organization","synonyms":[{"name":"activation of PSD organization","type":"narrow"},{"name":"activation of post synaptic density organization","type":"narrow"},{"name":"activation of post-synaptic density organization","type":"narrow"},{"name":"activation of postsynaptic density organisation","type":"narrow"},{"name":"activation of postsynaptic density organization","type":"narrow"},{"name":"positive regulation of PSD organization","type":"exact"},{"name":"positive regulation of post synaptic density organization","type":"exact"},{"name":"positive regulation of post-synaptic density organization","type":"exact"},{"name":"positive regulation of postsynaptic density organisation","type":"exact"},{"name":"up regulation of PSD organization","type":"exact"},{"name":"up regulation of post synaptic density organization","type":"exact"},{"name":"up regulation of post-synaptic density organization","type":"exact"},{"name":"up regulation of postsynaptic density organisation","type":"exact"},{"name":"up regulation of postsynaptic density organization","type":"exact"},{"name":"up-regulation of PSD organization","type":"exact"},{"name":"up-regulation of post synaptic density organization","type":"exact"},{"name":"up-regulation of post-synaptic density organization","type":"exact"},{"name":"up-regulation of postsynaptic density organisation","type":"exact"},{"name":"up-regulation of postsynaptic density organization","type":"exact"},{"name":"upregulation of PSD organization","type":"exact"},{"name":"upregulation of post synaptic density organization","type":"exact"},{"name":"upregulation of post-synaptic density organization","type":"exact"},{"name":"upregulation of postsynaptic density organisation","type":"exact"},{"name":"upregulation of postsynaptic density organization","type":"exact"}],"termid":"GO:1905876"}


id: PBO:0003690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-C3H1 type","termid":"PBO:0003690"}


id: PATO:0001660
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An action potential which is relatively low.","definition_xrefs":["PATOC:GVG"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001660 decreased action potential (obsolete PATO:0001660)","synonyms":[{"name":"low action potential","type":"exact"}],"termid":"PATO:0001660"}


id: PR:O13704
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mpd1 gene.","definition_xrefs":["UniProtKB:O13704","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":"thioredoxin domain-containing protein C13F5.05, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13F5.05","synonyms":[{"name":"Spom972h-mpd1","type":"exact"}],"termid":"PR:O13704"}


id: PBO:0030254
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_trehalose_level_during_vegetative_growth","termid":"PBO:0030254"}


id: PBO:0071149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 13","termid":"PBO:0071149"}


id: PBO:0001082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structure-specific endonuclease catalytic subunit","termid":"PBO:0001082"}


id: PBO:0120087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EXOC1 antisense RNA 1","termid":"PBO:0120087"}


id: GO:0032343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of aldosterone, a corticosteroid hormone that is produced by the zona glomerulosa of the adrenal cortex and regulates salt (sodium and potassium) and water balance.","definition_xrefs":["PMID:16527843"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mineralocorticoid catabolic process","termid":"GO:0006712"},{"relation_name":"is_a","term_name":"C21-steroid hormone catabolic process","termid":"GO:0008208"},{"relation_name":"is_a","term_name":"aldosterone metabolic process","termid":"GO:0032341"},{"relation_name":"is_a","term_name":"primary alcohol catabolic process","termid":"GO:0034310"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"aldehyde catabolic process","termid":"GO:0046185"},{"relation_name":"is_a","term_name":"olefinic compound catabolic process","termid":"GO:0120256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"aldosterone catabolic process","termid":"GO:0032343"}


id: SO:0000863
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute describing an mRNA feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_attribute","termid":"SO:0000237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA_attribute","synonyms":[{"name":"mRNA attribute","type":"exact"}],"termid":"SO:0000863"}


id: GO:0106141
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dimethylallyl phosphate + FMNH2 = phosphate + prenyl-FMNH2.","definition_xrefs":["RHEA:37743","PMID:26083743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenyltransferase activity","termid":"GO:0004659"}],"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"},{"rel_name":"is_a","termid":"GO:0016765"}],"interesting_parent_ids":["GO:0016765","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"flavin prenyltransferase activity","secondary_identifiers":["EC:2.5.1.129"],"termid":"GO:0106141"}


id: GO:0051334
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reformation of the nuclear membranes during meiosis I.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic nuclear membrane reassembly","termid":"GO:0051333"},{"relation_name":"part_of","term_name":"meiosis I","termid":"GO:0007127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0061024","GO:0008150","GO:0007049","GO:0140013","GO:0044085"],"is_obsolete":false,"name":"meiosis I nuclear membrane reassembly","synonyms":[{"name":"meiosis I nuclear envelope reassembly","type":"related"}],"termid":"GO:0051334"}


id: MONDO:0018642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A immunodeficiency disorder caused by loss of function mutation in NIK (MAP3K14).","definition_xrefs":["doi:10.1038/ncomms6360"],"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":"NIK deficiency","secondary_identifiers":["GARD:21864","MEDGEN:1808868","Orphanet:447731","UMLS:C5680065"],"synonyms":[{"name":"MAP3K14 non-severe combined immunodeficiency","type":"exact"},{"name":"non-severe combined immunodeficiency caused by mutation in MAP3K14","type":"exact"},{"name":"primary immunodeficiency with multifaceted aberrant lymphoid immunity","type":"exact"}],"termid":"MONDO:0018642","xrefs":{"Monarch":{"xref_id":"0018642"}}}


id: GO:1990535
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The organization process that preserves a neuron projection in a stable functional or structural state. A neuron projection is a prolongation or process extending from a nerve cell, e.g. an axon or dendrite.","definition_xrefs":["GOC:kmv","PMID:25359212"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection organization","termid":"GO:0106027"}],"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":"neuron projection maintenance","synonyms":[{"name":"axon homeostasis","type":"related"},{"name":"axon maintenance","type":"related"},{"name":"neurite maintenance","type":"narrow"},{"name":"neuron process maintenance","type":"exact"},{"name":"neuron protrusion maintenance","type":"exact"},{"name":"neuronal cell projection maintenance","type":"exact"}],"termid":"GO:1990535"}


id: PBO:0077060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombospondin type 1 domain containing 7A","termid":"PBO:0077060"}


id: PBO:0060125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 26","termid":"PBO:0060125"}


id: PBO:0068085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 391","termid":"PBO:0068085"}


id: PR:P87109
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phospholipase DDHD2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00563","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":"phospholipase C20G8.02, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC20G8.02","secondary_identifiers":["UniProtKB:P87109"],"synonyms":[{"name":"Spom972h-DDHD2","type":"exact"}],"termid":"PR:P87109"}


id: MONDO:0007660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of ossifying fibroma (disease) that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ossifying fibroma","termid":"MONDO:0002119"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial ossifying fibroma","secondary_identifiers":["UMLS:C3495361","GARD:17713","OMIM:137575","MESH:C563017","Orphanet:435329","MEDGEN:501159"],"synonyms":[{"name":"Cementomas, familial multiple","type":"related"},{"name":"GIGANTIFORM cementoma, familial","type":"related"},{"name":"Jaffe-Campanacci syndrome","type":"related"},{"name":"cemental dysplasia, periapical","type":"related"},{"name":"hereditary ossifying fibroma (disease)","type":"exact"},{"name":"intracortical fibrous dysplasia","type":"related"},{"name":"multiple ossifying fibroma","type":"exact"}],"termid":"MONDO:0007660","xrefs":{"Monarch":{"xref_id":"0007660"}}}


id: PBO:0072248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 23","termid":"PBO:0072248"}


id: PBO:0108761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase I termination factor Rtf1","termid":"PBO:0108761"}


id: GO:2000902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a cellooligosaccharide.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide metabolic process","termid":"GO:0009311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"cellooligosaccharide metabolic process","synonyms":[{"name":"cellooligosaccharide metabolism","type":"exact"}],"termid":"GO:2000902"}


id: PBO:0039252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase 3 family member A2","termid":"PBO:0039252"}


id: PATO:0000670
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000670 saccharin versus water value (obsolete PATO:0000670)","termid":"PATO:0000670"}


id: GO:0019364
data:
  {"annotated_genes":["SJAG_02945","SJAG_03373","SJAG_02135","SJAG_02785","SJAG_04334","SJAG_02796","SJAG_02369","SJAG_02009","SJAG_04048","SJAG_03660","SJAG_00839","SJAG_03828","SJAG_06621","SJAG_04495","SJAG_00027","SJAG_00605","SJAG_06622","SJAG_05314","SJAG_00461","SJAG_03903","SJAG_04192","SJAG_03091","SJAG_01310","SJAG_00685","SJAG_02107"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111237,79584,105202,96338,111240,111236,74174,111239,100077,105459,107650,107651,107281,99806,107280,107282,111238,111241,118208,111235],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"},{"annotations":[90422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061613"},{"annotations":[74133],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019677"},{"annotations":[74134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006742"},{"annotations":[77883,74826],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0045820"},{"annotations":[71755],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006110"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a pyridine nucleotide, a nucleotide characterized by a pyridine derivative as a nitrogen base.","definition_xrefs":["GOC:jl","GOC:vw","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide catabolic process","termid":"GO:0009166"},{"relation_name":"is_a","term_name":"pyridine nucleotide metabolic process","termid":"GO:0019362"},{"relation_name":"is_a","term_name":"pyridine-containing compound catabolic process","termid":"GO:0072526"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00461":null,"SJAG_00605":null,"SJAG_00685":null,"SJAG_00839":null,"SJAG_01310":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02369":null,"SJAG_02785":null,"SJAG_02796":null,"SJAG_02945":null,"SJAG_03091":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_04048":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_05314":null,"SJAG_06621":null,"SJAG_06622":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:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"pyridine nucleotide catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"pyridine nucleotide breakdown","type":"exact"},{"name":"pyridine nucleotide catabolism","type":"exact"},{"name":"pyridine nucleotide degradation","type":"exact"}],"termid":"GO:0019364","terms_by_termid":{"GO:0006110":null,"GO:0006742":null,"GO:0019677":null,"GO:0045820":null,"GO:0061613":null,"GO:0061621":null}}


id: MONDO:0000226
data:
  {"annotated_genes":["SJAG_01612","SJAG_03475","SJAG_02805","SJAG_03866","SJAG_01216","SJAG_03316","SJAG_02397","SJAG_01147","SJAG_04757","SJAG_02895","SJAG_03701","SJAG_02463","SJAG_02117","SJAG_02007","SJAG_04425","SJAG_01164","SJAG_05277","SJAG_03556","SJAG_00084","SJAG_03069","SJAG_02306","SJAG_00988","SJAG_03671","SJAG_01351","SJAG_01070","SJAG_01162","SJAG_03553","SJAG_01199","SJAG_04016","SJAG_01063","SJAG_03290","SJAG_03712","SJAG_03659","SJAG_03222","SJAG_03641","SJAG_00582","SJAG_04459","SJAG_01941","SJAG_04042","SJAG_01417","SJAG_01466","SJAG_00115","SJAG_01995"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009825"},{"annotations":[86983,86982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010966"},{"annotations":[87416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100255"},{"annotations":[88533,88534],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009727"},{"annotations":[87110],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009352"},{"annotations":[86806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009058"},{"annotations":[88589,88590],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009107"},{"annotations":[88824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015003"},{"annotations":[87259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010926"},{"annotations":[88016,88015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009285"},{"annotations":[87691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009259"},{"annotations":[87564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009947"},{"annotations":[88000],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009284"},{"annotations":[87291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011417"},{"annotations":[88662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019531"},{"annotations":[88067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009666"},{"annotations":[87054,87055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009353"},{"annotations":[88715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013404"},{"annotations":[88738,88737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011706"},{"annotations":[88439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013762"},{"annotations":[87226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014576"},{"annotations":[87755],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009607"},{"annotations":[87031,87032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009354"},{"annotations":[87642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009609"},{"annotations":[88473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"},{"annotations":[87534,87535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009189"},{"annotations":[86927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011582"},{"annotations":[88648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0975806"},{"annotations":[87454],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013675"},{"annotations":[87810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014132"},{"annotations":[87075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014611"},{"annotations":[87141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033282"},{"annotations":[87783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054785"},{"annotations":[88134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957382"},{"annotations":[88803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0971174"},{"annotations":[88723],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010476"},{"annotations":[87418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014290"},{"annotations":[86994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009529"},{"annotations":[87583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014803"},{"annotations":[87094,87095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019666"},{"annotations":[86934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009593"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"gene_count":43,"genes_by_uniquename":{"SJAG_00084":null,"SJAG_00115":null,"SJAG_00582":null,"SJAG_00988":null,"SJAG_01063":null,"SJAG_01070":null,"SJAG_01147":null,"SJAG_01162":null,"SJAG_01164":null,"SJAG_01199":null,"SJAG_01216":null,"SJAG_01351":null,"SJAG_01417":null,"SJAG_01466":null,"SJAG_01612":null,"SJAG_01941":null,"SJAG_01995":null,"SJAG_02007":null,"SJAG_02117":null,"SJAG_02306":null,"SJAG_02397":null,"SJAG_02463":null,"SJAG_02805":null,"SJAG_02895":null,"SJAG_03069":null,"SJAG_03222":null,"SJAG_03290":null,"SJAG_03316":null,"SJAG_03475":null,"SJAG_03553":null,"SJAG_03556":null,"SJAG_03641":null,"SJAG_03659":null,"SJAG_03671":null,"SJAG_03701":null,"SJAG_03712":null,"SJAG_03866":null,"SJAG_04016":null,"SJAG_04042":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04757":null,"SJAG_05277":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"mineral metabolism disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:E83","ICD9:275.9","EFO:0009556","ICD9:275.8","MEDGEN:509562","SCTID:45744005","UMLS:C0154260"],"synonyms":[{"name":"disease of mineral metabolism","type":"exact"},{"name":"disorder of mineral metabolism","type":"exact"}],"termid":"MONDO:0000226","terms_by_termid":{"MONDO:0009058":null,"MONDO:0009107":null,"MONDO:0009189":null,"MONDO:0009259":null,"MONDO:0009284":null,"MONDO:0009285":null,"MONDO:0009352":null,"MONDO:0009353":null,"MONDO:0009354":null,"MONDO:0009529":null,"MONDO:0009593":null,"MONDO:0009607":null,"MONDO:0009609":null,"MONDO:0009666":null,"MONDO:0009727":null,"MONDO:0009825":null,"MONDO:0009947":null,"MONDO:0010184":null,"MONDO:0010476":null,"MONDO:0010926":null,"MONDO:0010966":null,"MONDO:0011417":null,"MONDO:0011582":null,"MONDO:0011706":null,"MONDO:0013404":null,"MONDO:0013675":null,"MONDO:0013762":null,"MONDO:0014132":null,"MONDO:0014290":null,"MONDO:0014576":null,"MONDO:0014611":null,"MONDO:0014803":null,"MONDO:0015003":null,"MONDO:0019531":null,"MONDO:0019666":null,"MONDO:0033282":null,"MONDO:0054785":null,"MONDO:0100255":null,"MONDO:0957382":null,"MONDO:0971174":null,"MONDO:0975806":null},"xrefs":{"Monarch":{"xref_id":"0000226"}}}


id: MONDO:0003151
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete movement disease (obsolete MONDO:0003151)","termid":"MONDO:0003151","xrefs":{"Monarch":{"xref_id":"0003151"}}}


id: PBO:0078242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 22-1 (pseudogene)","termid":"PBO:0078242"}


id: PBO:0001008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation protein (predicted)","termid":"PBO:0001008"}


id: PBO:0059158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallophosphoesterase domain containing 2","termid":"PBO:0059158"}


id: PBO:0002577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster assembly ATPase Nbp35 (predicted)","termid":"PBO:0002577"}


id: PBO:0039947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AT-rich interaction domain 5B","termid":"PBO:0039947"}


id: PBO:0071460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 1","termid":"PBO:0071460"}


id: FYPO:0005311
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 methylation of lysine at position 4 of histone H3 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone methylation during vegetative growth","termid":"FYPO:0000861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal histone H3-K4 methylation during vegetative growth","synonyms":[{"name":"normal histone H3 K4 methylation during vegetative growth","type":"exact"},{"name":"normal histone H3-K4 methylation during mitotic cell cycle","type":"related"},{"name":"normal histone H3K4me during vegetative growth","type":"exact"},{"name":"normal histone lysine H3 K4 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0005311"}


id: PBO:0065372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"presenilin enhancer, gamma-secretase subunit","termid":"PBO:0065372"}


id: PBO:0071420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 26","termid":"PBO:0071420"}


id: PBO:0002947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA U24","termid":"PBO:0002947"}


id: PBO:0054712
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 2121","termid":"PBO:0054712"}


id: PBO:0071592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 9","termid":"PBO:0071592"}


id: PBO:0057749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1908","termid":"PBO:0057749"}


id: PBO:0062084
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 15","termid":"PBO:0062084"}


id: PBO:0113169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Integral membrane protein required for efficient mating; may participate in or regulate the low affinity Ca2+ influx system, which affects intracellular signaling and cell-cell fusion during mating; targeted to vacuole via AP-3 pathway","termid":"PBO:0113169"}


id: PBO:0091871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"agmatinase 2","termid":"PBO:0091871"}


id: GO:0004603
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + phenylethanolamine = S-adenosyl-L-homocysteine + N-methylphenylethanolamine.","definition_xrefs":["EC:2.1.1.28"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-methyltransferase activity","termid":"GO:0008170"},{"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:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016741","GO:0003674"],"is_obsolete":false,"name":"phenylethanolamine N-methyltransferase activity","secondary_identifiers":["MetaCyc:2.1.1.28-RXN","Reactome:R-HSA-209903","RHEA:12176"],"synonyms":[{"name":"S-adenosyl-L-methionine:phenylethanolamine N-methyltransferase activity","type":"related"},{"name":"noradrenalin N-methyltransferase activity","type":"related"},{"name":"noradrenaline N-methyltransferase activity","type":"related"},{"name":"norepinephrine N-methyltransferase activity","type":"related"},{"name":"norepinephrine methyltransferase activity","type":"related"},{"name":"phenethanolamine N-methyltransferase activity","type":"related"},{"name":"phenethanolamine methyltransferase activity","type":"related"}],"termid":"GO:0004603"}


id: GO:0003106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which angiotensin directly decreases the rate of glomerular filtration in the kidney. Glomerular filtration is the process whereby blood is filtered by the glomerulus into the renal tubule.","definition_xrefs":["GOC:dph","GOC:tb","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of renal output by angiotensin","termid":"GO:0003083"},{"relation_name":"part_of","term_name":"negative regulation of glomerular filtration","termid":"GO:0003105"}],"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 glomerular filtration by angiotensin","synonyms":[{"name":"angiotensin-mediated regulation of glomerular filtration","type":"broad"},{"name":"regulation of glomerular filtration by angiotensin","type":"broad"}],"termid":"GO:0003106"}


id: PBO:0052643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 11","termid":"PBO:0052643"}


id: GO:0005604
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen-containing extracellular matrix consisting of a thin layer of dense material found in various animal tissues interposed between the cells and the adjacent connective tissue. It consists of the basal lamina plus an associated layer of reticulin fibers.","definition_xrefs":["PMID:33605520","PMID:22505934","PMID:39223427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix","termid":"GO:0031012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"basement membrane","secondary_identifiers":["Wikipedia:Basement_membrane","GO:0008003","GO:0005605"],"synonyms":[{"name":"basal lamina","type":"related"},{"name":"basement lamina","type":"related"},{"name":"lamina densa","type":"related"}],"termid":"GO:0005604"}


id: GO:0002240
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus by molecules of oomycetes origin.","definition_xrefs":["GOC:sm","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to external biotic stimulus","termid":"GO:0043207"},{"relation_name":"part_of","term_name":"response to oomycetes","termid":"GO:0002239"}],"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 molecule of oomycetes origin","synonyms":[{"name":"response to oomycetes associated molecule","type":"exact"}],"termid":"GO:0002240"}


id: PBO:0088227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L8/L2","termid":"PBO:0088227"}


id: GO:0062122
data:
  {"annotated_genes":["SJAG_03487"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58335],"is_not":false,"summary":null,"term":"GO:0062122"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + histone H3 L-lysine (position 37) = S-adenosyl-L-homocysteine + histone H3 N6-methyl-L-lysine (position 37). This reaction is the addition of a methyl group to the lysine residue at position 37 of the histone H3 protein.","definition_xrefs":["PMID:30773398"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-lysine N-methyltransferase activity","termid":"GO:0016279"},{"relation_name":"is_a","term_name":"histone H3 methyltransferase activity","termid":"GO:0140938"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03487":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016741","GO:0003824","GO:0140096","GO:0008276"],"is_obsolete":false,"name":"histone H3K37 methyltransferase activity","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"histone H3K37 methylase activity","type":"exact"},{"name":"histone lysine N-methyltransferase activity (H3-K37 specific)","type":"exact"},{"name":"histone methyltransferase activity (H3-K37 specific)","type":"exact"},{"name":"histone-H3K37 methyltransferase activity","type":"exact"}],"termid":"GO:0062122","terms_by_termid":{"GO:0062122":null}}


id: PBO:0075277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 19 pseudogene 2","termid":"PBO:0075277"}


id: FYPO:0000212
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the cellular response to heat is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to stress during vegetative growth","termid":"FYPO:0001341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0000298"],"is_obsolete":false,"name":"abnormal cellular response to heat","synonyms":[{"name":"abnormal cellular response to heat during mitotic cell cycle","type":"related"},{"name":"abnormal cellular response to heat during vegetative growth","type":"exact"}],"termid":"FYPO:0000212"}


id: PBO:0089791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L59","termid":"PBO:0089791"}


id: PBO:0062777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 56 subfamily A member 5","termid":"PBO:0062777"}


id: PBO:0041224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1 open reading frame 21","termid":"PBO:0041224"}


id: PBO:0069697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 976, pseudogene","termid":"PBO:0069697"}


id: FYPO:0005083
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at non-coding RNA (ncRNA) genes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:21151114","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin during vegetative growth","termid":"FYPO:0001509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"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:0000138","FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to chromatin at ncRNA gene","synonyms":[{"name":"normal protein localisation to chromatin at ncRNA gene","type":"exact"},{"name":"normal protein localization to chromatin at ncRNA gene during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at ncRNA gene during vegetative growth","type":"exact"}],"termid":"FYPO:0005083"}


id: FYPO:0005683
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through prophase of mitosis is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of mitotic cell cycle phase","termid":"FYPO:0001069"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000631","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased duration of mitotic prophase","synonyms":[{"name":"delayed mitotic prophase progression","type":"related"},{"name":"increased duration of mitotic prophase during vegetative growth","type":"exact"},{"name":"increased duration of mitotic prophase progression","type":"exact"},{"name":"increased duration of prophase during mitotic cell cycle","type":"exact"},{"name":"prolonged mitotic prophase","type":"exact"}],"termid":"FYPO:0005683"}


id: MONDO:0007961
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"megalencephaly","termid":"MONDO:0016608"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megalencephaly, autosomal dominant","secondary_identifiers":["OMIM:155350","UMLS:C3805727","MEDGEN:812057"],"synonyms":[{"name":"megalencephaly, autosomal dominant","type":"exact"}],"termid":"MONDO:0007961","xrefs":{"Monarch":{"xref_id":"0007961"}}}


id: MONDO:0100000
data:
  {"annotated_genes":["SJAG_00156"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88725],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010477"},{"annotations":[88945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010590"},{"annotations":[86819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010655"}]},"cv_name":"mondo","definition":"An X-linked syndromic intellectual disability that that includes subtypes of the heterogeneous, eponymously named Lujan-Fryns syndrome, X-linked Ohdo syndrome, and Optiz-Kaveggia/ FG syndrome, which is caused by mutations in the gene MED12. The common and most penetrant phenotype shared amongst these disease entities is intellectual disability, with dysgenesis or agenesis of the corpus callosum, blepharophimosis, and marfanoid habitus having variable phenotypic expressivity.","definition_xrefs":["PMID:20301719"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00156":null},"genotype_count":0,"is_obsolete":false,"name":"MED12-related intellectual disability syndrome","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"MED12 X-linked syndromic intellectual disability","type":"exact"},{"name":"MED12-related intellectual disability syndrome","type":"exact"},{"name":"X-linked syndromic intellectual disability caused by mutation in MED12","type":"exact"}],"termid":"MONDO:0100000","terms_by_termid":{"MONDO:0010477":null,"MONDO:0010590":null,"MONDO:0010655":null},"xrefs":{"Monarch":{"xref_id":"0100000"}}}


id: PBO:0085554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein containing a C-terminal SH3 domain; binds Las17p, which is a homolog of human Wiskott-Aldrich Syndrome protein involved in actin patch assembly and actin polymerization; protein abundance increases in response to DNA replication stress; LSB3 has a paralog, YSC84, that arose from the whole genome duplication","termid":"PBO:0085554"}


id: GO:2000391
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of neutrophil extravasation.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular extravasation","termid":"GO:0002693"},{"relation_name":"is_a","term_name":"positive regulation of neutrophil migration","termid":"GO:1902624"},{"relation_name":"is_a","term_name":"regulation of neutrophil extravasation","termid":"GO:2000389"},{"relation_name":"positively_regulates","term_name":"neutrophil extravasation","termid":"GO:0072672"}],"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 neutrophil extravasation","termid":"GO:2000391"}


id: PBO:0043373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clustered mitochondria homolog pseudogene 3","termid":"PBO:0043373"}


id: PBO:0028670
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_number_of_Kms1_foci","termid":"PBO:0028670"}


id: PBO:0026898
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_phosphorylation_during_nitrogen_starvation","termid":"PBO:0026898"}


id: PBO:0046714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eva-1 homolog C","termid":"PBO:0046714"}


id: GO:0006567
data:
  {"annotated_genes":["SJAG_02450"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73863],"is_not":false,"summary":null,"term":"GO:0006567"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-threonine (2-amino-3-hydroxybutyric acid), a polar, uncharged, essential amino acid found in peptide linkage in proteins.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"threonine metabolic process","termid":"GO:0006566"},{"relation_name":"is_a","term_name":"aspartate family amino acid catabolic process","termid":"GO:0009068"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02450":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"L-threonine catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["UM-BBD_pathwayID:met"],"synonyms":[{"name":"threonine breakdown","type":"exact"},{"name":"threonine catabolism","type":"exact"},{"name":"threonine degradation","type":"exact"}],"termid":"GO:0006567","terms_by_termid":{"GO:0006567":null}}


id: PBO:0041865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase 10","termid":"PBO:0041865"}


id: GO:0099575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates synaptic transmission by regulating a catabolic process occurring at a presynapse.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein catabolic process","termid":"GO:0042176"},{"relation_name":"is_a","term_name":"presynaptic modulation of chemical synaptic transmission","termid":"GO:0099171"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0030163"],"is_obsolete":false,"name":"regulation of protein catabolic process at presynapse, modulating synaptic transmission","termid":"GO:0099575"}


id: GO:0031526
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the plasma membrane surrounding the brush border.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell projection membrane","termid":"GO:0031253"},{"relation_name":"part_of","term_name":"brush border","termid":"GO:0005903"},{"relation_name":"part_of","term_name":"apical plasma membrane","termid":"GO:0016324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"brush border membrane","termid":"GO:0031526"}


id: PBO:0074687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 67","termid":"PBO:0074687"}


id: MONDO:0002162
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare malignant neoplasm that arises from the fallopian tube and is characterized by the presence of a benign epithelial component and a sarcomatous component.","definition_xrefs":["NCIT:C40125"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"fallopian tube carcinosarcoma","termid":"MONDO:0006207"},{"relation_name":"is_a","term_name":"fallopian tube cancer","termid":"MONDO:0002158"},{"relation_name":"is_a","term_name":"adenosarcoma","termid":"MONDO:0005636"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"fallopian tube adenosarcoma","secondary_identifiers":["DOID:1973","MEDGEN:275872","UMLS:C1517121"],"synonyms":[{"name":"adenosarcoma of fallopian tube","type":"exact"},{"name":"fallopian tube Mullerian adenosarcoma","type":"exact"},{"name":"fallopian tube Müllerian adenosarcoma","type":"exact"},{"name":"fallopian tube adenosarcoma","type":"exact"},{"name":"fallopian tube mullerian adenosarcoma","type":"exact"}],"termid":"MONDO:0002162","xrefs":{"Monarch":{"xref_id":"0002162"}}}


id: PBO:0048570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GGCT pseudogene 3","termid":"PBO:0048570"}


id: GO:0052322
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of phytoalexin biosynthesis, the chemical reactions and pathways resulting in the formation of phytoalexins.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"defense response to symbiont","termid":"GO:0140546"},{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"positively_regulates","term_name":"phytoalexin biosynthetic process","termid":"GO:0052315"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"positive regulation of phytoalexin biosynthetic process","synonyms":[{"name":"activation of phytoalexin biosynthesis","type":"narrow"},{"name":"positive regulation of phytoalexin biosynthesis","type":"exact"},{"name":"stimulation of phytoalexin biosynthesis","type":"narrow"},{"name":"up regulation of phytoalexin biosynthesis","type":"exact"},{"name":"up-regulation of phytoalexin biosynthesis","type":"exact"},{"name":"upregulation of phytoalexin biosynthesis","type":"exact"}],"termid":"GO:0052322"}


id: PBO:0031839
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_shmoo_morphology","termid":"PBO:0031839"}


id: PBO:0017972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IMPACT domain protein, possible chaperone, regulation of cytoplasmic translation in response to stress (predicted)","termid":"PBO:0017972"}


id: GO:0010233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of substances, into, out of or within the phloem during long distance transport between source and sink tissues.","definition_xrefs":["PMID:19025382","GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular transport","termid":"GO:0010232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"phloem transport","termid":"GO:0010233"}


id: SO:0000809
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A cDNA clone that is invalid.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"invalidated","termid":"SO:0000790"},{"relation_name":"is_a","term_name":"cDNA_clone","termid":"SO:0000317"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"invalidated_cDNA_clone","synonyms":[{"name":"invalidated cDNA clone","type":"exact"}],"termid":"SO:0000809"}


id: PBO:0050946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon alpha 20, pseudogene","termid":"PBO:0050946"}


id: _global:exists_during
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","direct_ancestors":[{"relation_name":"is_a","term_name":"during","termid":"_global:during"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exists_during","secondary_identifiers":["GOREL:0000032"],"synonyms":[{"name":"during","type":"broad"}],"termid":"_global:exists_during"}


id: MONDO:0968946
data:
  {"annotated_genes":["SJAG_04936"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88976],"is_not":false,"summary":null,"term":"MONDO:0968946"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"genetic developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04936":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy 115","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1858870","UMLS:C5935604","OMIM:620783"],"termid":"MONDO:0968946","terms_by_termid":{"MONDO:0968946":null},"xrefs":{"Monarch":{"xref_id":"0968946"}}}


id: PBO:0030067
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cell_population_growth_on_gluconate_carbon_source","termid":"PBO:0030067"}


id: PBO:0038373
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_exposure_route","termid":"PBO:0038373"}


id: GO:0047897
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7,8-dihydrofolate + ATP + formate = 10-formyldihydrofolate + ADP + H+ + phosphate.","definition_xrefs":["EC:6.3.4.17","RHEA:24328"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"formate-dihydrofolate ligase activity","secondary_identifiers":["MetaCyc:FORMATE--DIHYDROFOLATE-LIGASE-RXN","KEGG_REACTION:R02238"],"synonyms":[{"name":"dihydrofolate formyltransferase activity","type":"related"},{"name":"formate:dihydrofolate ligase (ADP-forming)","type":"related"},{"name":"formyl dihydrofolate synthase activity","type":"related"}],"termid":"GO:0047897"}


id: FYPO:0005069
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid segregation fails to separate chromosomes into two equal masses after the cell has undergone a normal mitotic nuclear division and passed through the subsequent mitotic interphase. Unequal mitotic sister chromatid separation may be complete, with two distinct unequal DNA masses located at or near the ends of an elongated mitotic spindle, or incomplete.","definition_xrefs":["PMID:18180284","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unequal mitotic sister chromatid segregation","termid":"FYPO:0003241"},{"relation_name":"is_a","term_name":"abnormal mitosis following normal mitosis","termid":"FYPO:0004588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0000337","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000631","FYPO:0001985"],"is_obsolete":false,"name":"unequal mitotic sister chromatid segregation following normal mitosis","synonyms":[{"name":"mitotic chromosome nondisjunction following normal mitosis","type":"exact"},{"name":"unequal mitotic chromosome segregation following normal mitosis","type":"exact"},{"name":"unequal mitotic sister chromatid segregation during vegetative growth following normal mitosis","type":"exact"},{"name":"unequal mitotic sister chromatid separation following normal mitosis","type":"related"},{"name":"unequal sister chromatid segregation following normal mitosis during mitotic cell cycle","type":"related"}],"termid":"FYPO:0005069"}


id: PBO:0091293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA initiator Methionine","termid":"PBO:0091293"}


id: FYECO:0000056
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which 3'5'-cyclic AMP was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["CHEBI:17489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 3,5-cyclic AMP","termid":"FYECO:0000056"}


id: MONDO:0008272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polysyndactyly or PPD4 is a form of preaxial polydactyly of fingers, a limb malformation syndrome, characterized by the presence of a thumb showing the mildest degree of duplication, being broad, bifid or with radially deviated distal phalanx. Syndactyly of various degrees of third-and-fourth fingers is occasionally present.","definition_xrefs":["Orphanet:93338"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"metabolic disease","termid":"MONDO:0005066"},{"relation_name":"is_a","term_name":"non-syndromic synpolydactyly","termid":"MONDO:0000722"},{"relation_name":"is_a","term_name":"preaxial polydactyly of fingers","termid":"MONDO:0017425"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"polysyndactyly 4","secondary_identifiers":["OMIM:174700","GARD:9903","ICD9:755.10","MedDRA:10063143","MEDGEN:357420","UMLS:C1868111","icd11.foundation:973656080"],"synonyms":[{"name":"PPD4","type":"exact"},{"name":"crossed polydactyly type 1","type":"related"},{"name":"crossed polydactyly, type 1","type":"related"},{"name":"polydactyly preaxial 4","type":"related"},{"name":"polydactyly, preaxial 4","type":"related"},{"name":"polydactyly, preaxial IV","type":"related"},{"name":"polydactyly, preaxial type 4","type":"exact"},{"name":"polydactyly, preaxial, type IV","type":"exact"},{"name":"polysyndactyly uncomplicated","type":"related"},{"name":"polysyndactyly, uncomplicated","type":"related"},{"name":"preaxial polydactyly 4","type":"related"},{"name":"preaxial polydactyly type 4","type":"exact"}],"termid":"MONDO:0008272","xrefs":{"Monarch":{"xref_id":"0008272"}}}


id: PATO:0002275
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color pattern quality inhering in a bearer by virtue of the bearer's color pattern in which light and dark colors (for example white and black) are codistributed to create a visual impression.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color pattern","termid":"PATO:0000019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high contrast color pattern","termid":"PATO:0002275"}


id: PBO:0113759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein, lipocalin-like","termid":"PBO:0113759"}


id: PR:Q9URV6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tim11 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9URV6"],"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":"ATP synthase subunit e, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC106.05c","synonyms":[{"name":"ATPase subunit e (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-tim11","type":"exact"},{"name":"translocase of the inner membrane protein 11 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9URV6"}


id: GO:0071128
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha5-beta1 integrin complex bound to osteopontin.","definition_xrefs":["PMID:16005200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"alpha5-beta1 integrin-osteopontin complex","synonyms":[{"name":"ITGA5-ITGB1-SPP1 complex","type":"narrow"}],"termid":"GO:0071128"}


id: PBO:0029606
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-transporter_activity_phenotype","termid":"PBO:0029606"}


id: GO:0102995
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: columbianetin + NADPH + O2 + H+ = angelicin + acetone + NADP + 2 H2O.","definition_xrefs":["EC:1.14.14.148","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"angelicin synthase activity","secondary_identifiers":["RHEA:27481","MetaCyc:RXN-9689"],"termid":"GO:0102995"}


id: MONDO:0004953
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The most common type of invasive breast carcinoma, accounting for approximately 70% of breast carcinomas. The gross appearance is usually typical with an irregular stellate outline. Microscopically, randomly arranged epithelial elements are seen. When large sheets of malignant cells are present, necrosis may be seen. With adequate tissue sampling, in situ carcinoma can be demonstrated in association with the infiltrating carcinoma. The in situ component is nearly always ductal but occasionally may be lobular or both.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast ductal adenocarcinoma","termid":"MONDO:0005590"},{"relation_name":"is_a","term_name":"invasive breast carcinoma","termid":"MONDO:0006256"}],"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 ductal breast carcinoma","secondary_identifiers":["SCTID:408643008","MEDGEN:730612","ICDO:8521/3","DOID:3008","ICD9:174.8","EFO:0000186","NCIT:C4194","ONCOTREE:IDC","UMLS:C1412014","ICDO:8500/3"],"synonyms":[{"name":"breast invasive ductal carcinoma","type":"related"},{"name":"ductal adenocarcinoma","type":"exact"},{"name":"infiltrating ductal adenocarcinoma","type":"exact"},{"name":"infiltrating ductal breast carcinoma","type":"exact"},{"name":"infiltrating ductal carcinoma","type":"exact"},{"name":"infiltrating ductal carcinoma of breast","type":"exact"},{"name":"infiltrating ductal carcinoma of the breast","type":"exact"},{"name":"invasive ductal adenocarcinoma","type":"exact"},{"name":"invasive ductal breast carcinoma","type":"exact"},{"name":"invasive ductal carcinoma","type":"exact"},{"name":"invasive ductal carcinoma of breast","type":"exact"},{"name":"invasive ductal carcinoma of the breast","type":"exact"},{"name":"invasive ductal carcinoma, NST","type":"exact"},{"name":"invasive ductal carcinoma, No specific type","type":"exact"}],"termid":"MONDO:0004953","xrefs":{"Monarch":{"xref_id":"0004953"}}}


id: GO:1904094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of autophagic cell death.","definition_xrefs":["GOC:bhm","GOC:TermGenie","GO_REF:0000058","PMID:25736836"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of programmed cell death","termid":"GO:0043068"},{"relation_name":"is_a","term_name":"regulation of autophagic cell death","termid":"GO:1904092"},{"relation_name":"positively_regulates","term_name":"autophagic cell death","termid":"GO:0048102"}],"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 autophagic cell death","synonyms":[{"name":"activation of autophagic cell death","type":"narrow"},{"name":"activation of programmed cell death by macroautophagy","type":"narrow"},{"name":"activation of type II programmed cell death","type":"related"},{"name":"positive regulation of programmed cell death by macroautophagy","type":"exact"},{"name":"positive regulation of type II programmed cell death","type":"related"},{"name":"up regulation of autophagic cell death","type":"exact"},{"name":"up regulation of programmed cell death by macroautophagy","type":"exact"},{"name":"up regulation of type II programmed cell death","type":"related"},{"name":"up-regulation of autophagic cell death","type":"exact"},{"name":"up-regulation of programmed cell death by macroautophagy","type":"exact"},{"name":"up-regulation of type II programmed cell death","type":"related"},{"name":"upregulation of autophagic cell death","type":"exact"},{"name":"upregulation of programmed cell death by macroautophagy","type":"exact"},{"name":"upregulation of type II programmed cell death","type":"related"}],"termid":"GO:1904094"}


id: GO:0033705
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GDP-6-deoxy-D-mannose + NAD(P)+ = GDP-4-dehydro-6-deoxy-D-mannose + NAD(P)H + H+.","definition_xrefs":["EC:1.1.1.281"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"GDP-4-dehydro-6-deoxy-D-mannose reductase activity","synonyms":[{"name":"GDP-4-keto-6-deoxy-D-mannose reductase activity","type":"broad"},{"name":"GDP-6-deoxy-D-lyxo-4-hexulose reductase activity","type":"related"},{"name":"GDP-6-deoxy-D-mannose:NAD(P)+ 4-oxidoreductase (D-rhamnose-forming) activity","type":"related"},{"name":"Rmd","type":"related"}],"termid":"GO:0033705"}


id: PBO:0005836
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid adenoma","termid":"PBO:0005836"}


id: PBO:0059138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MPHOSPH10 pseudogene 5","termid":"PBO:0059138"}


id: PBO:0054228
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 1610","termid":"PBO:0054228"}


id: PR:P49373
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tfs1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P49373"],"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 elongation factor S-II (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC20H4.03c","synonyms":[{"name":"Spom972h-tfs1","type":"exact"},{"name":"TFIIS (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P49373"}


id: GO:0089700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A series of reactions, mediated by the intracellular serine/threonine kinase protein kinase D, which occurs as a result of a single trigger reaction or compound.","definition_xrefs":["GOC:BHF","GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete protein kinase D signaling (obsolete GO:0089700)","synonyms":[{"name":"PKD signal transduction","type":"exact"},{"name":"PKD signaling cascade","type":"related"},{"name":"protein kinase D signal transduction","type":"exact"},{"name":"protein kinase D signaling cascade","type":"related"},{"name":"protein kinase D signalling cascade","type":"related"}],"termid":"GO:0089700"}


id: MONDO:0021188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hemangiopericytoma (obsolete MONDO:0021188)","termid":"MONDO:0021188","xrefs":{"Monarch":{"xref_id":"0021188"}}}


id: GO:0045477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of nurse cell apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis","PMID:11973306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process involved in development","termid":"GO:1904748"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"nurse cell apoptotic process","termid":"GO:0045476"}],"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 nurse cell apoptotic process","synonyms":[{"name":"regulation of nurse cell apoptosis","type":"narrow"}],"termid":"GO:0045477"}


id: FYPO:0004998
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of horsetail movement is shorter than normal. Horsetail movement is the oscillatory movement of the nucleus that takes place during meiotic prophase I.","definition_xrefs":["GO:0030989","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal horsetail movement","termid":"FYPO:0000197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0000631"],"is_obsolete":false,"name":"decreased duration of horsetail movement","synonyms":[{"name":"decreased duration of dynein-driven meiotic oscillatory nuclear movement","type":"exact"},{"name":"decreased duration of horsetail nuclear movement","type":"exact"},{"name":"reduced duration of horsetail movement","type":"exact"}],"termid":"FYPO:0004998"}


id: PBO:0038542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 15","termid":"PBO:0038542"}


id: PBO:0071667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L37a pseudogene 8","termid":"PBO:0071667"}


id: GO:0045329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of carnitine (hydroxy-trimethyl aminobutyric acid), a compound that participates in the transfer of acyl groups across the inner mitochondrial membrane.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid betaine biosynthetic process","termid":"GO:0006578"},{"relation_name":"is_a","term_name":"carnitine metabolic process","termid":"GO:0009437"}],"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":"carnitine biosynthetic process","secondary_identifiers":["Reactome:R-HSA-71262"],"synonyms":[{"name":"carnitine anabolism","type":"exact"},{"name":"carnitine biosynthesis","type":"exact"},{"name":"carnitine formation","type":"exact"},{"name":"carnitine synthesis","type":"exact"},{"name":"vitamin Bt biosynthesis","type":"exact"},{"name":"vitamin Bt biosynthetic process","type":"exact"}],"termid":"GO:0045329"}


id: PBO:0047961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FRAT regulator of WNT signaling pathway 1","termid":"PBO:0047961"}


id: MONDO:0015809
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A variant of mycosis fungoides, characterized by an exclusively intraepidermal atypical (cerebriform) lymphocytic infiltrate. Patients present with a localized psoriasiform or hyperkeratotic patch or plaque, usually in the extremities. Extracutaneous dissemination of the disease has never been reported.","definition_xrefs":["NCIT:C35794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mycosis fungoides variant","termid":"MONDO:0045071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"localized pagetoid reticulosis","secondary_identifiers":["MESH:D056267","ICD10CM:C84.0","Orphanet:178517","ICD9:202.70","GARD:20155","MEDGEN:699349","SCTID:404120006","UMLS:C1276140"],"synonyms":[{"name":"localised reticulosis","type":"exact"},{"name":"localized reticulosis","type":"exact"},{"name":"pagetoid reticulosis","type":"exact"},{"name":"pagetoid reticulosis, Woringer-Kolopp type","type":"exact"}],"termid":"MONDO:0015809","xrefs":{"Monarch":{"xref_id":"0015809"}}}


id: MONDO:1010072
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Factor X deficiency that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"factor X deficiency, non-human animal","secondary_identifiers":["OMIA:000362"],"termid":"MONDO:1010072","xrefs":{"Monarch":{"xref_id":"1010072"}}}


id: PBO:0045400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPPA3 pseudogene 2","termid":"PBO:0045400"}


id: GO:0036009
data:
  {"annotated_genes":["SJAG_02350","SJAG_03949","SJAG_00286","SJAG_00943"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75030,112046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990259"},{"annotations":[97317,98297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102559"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-glutaminyl-[protein] + S-adenosyl-L-methionine = N(5)-methyl-L-glutaminyl-[protein] + S-adenosyl-L-homocysteine + H+.","definition_xrefs":["PMID:11847124","RHEA:57452"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-methyltransferase activity","termid":"GO:0008170"},{"relation_name":"is_a","term_name":"protein methyltransferase activity","termid":"GO:0008276"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00286":null,"SJAG_00943":null,"SJAG_02350":null,"SJAG_03949":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0016741","GO:0016740","GO:0008276","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"protein-glutamine N-methyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-6800138"],"synonyms":[{"name":"protein glutamine N-methylase activity","type":"exact"},{"name":"protein glutamine N-methyltransferase activity","type":"exact"}],"termid":"GO:0036009","terms_by_termid":{"GO:0102559":null,"GO:1990259":null}}


id: PATO:0000544
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000544 light_quality sensitivity value (obsolete PATO:0000544)","termid":"PATO:0000544"}


id: RO:0002254
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x has developmental contribution from y iff x has some part z such that z develops from y","direct_ancestors":[{"relation_name":"is_a","term_name":"developmentally_preceded_by","termid":"RO:0002258"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_developmental_contribution_from","termid":"RO:0002254"}


id: MOD:00221
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks L-aspartic acid and L-cysteine residues via an isopeptide bond to form N-(L-isoaspartyl)-L-cysteine.","definition_xrefs":["PubMed:8286361","RESID:AA0216"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked L-asparagine residue","termid":"MOD:02042"},{"relation_name":"is_a","term_name":"crosslinked L-cysteine residue","termid":"MOD:02044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"N-(L-isoaspartyl)-L-cysteine","synonyms":[{"name":"(S)-2-amino-4-((R)-1-carboxy-2-sulfanylethyl)amino-4-oxobutanoic acid","type":"exact"},{"name":"2-(3-amino-3-carboxypropanoyl)amino-3-mercaptopropanoic acid","type":"exact"},{"name":"2-amino-N4-(1-carboxy-2-mercaptoethyl)butanediamic acid","type":"exact"},{"name":"CROSSLNK Isoaspartyl cysteine isopeptide (Cys-Asn)","type":"exact"},{"name":"N-(L-isoaspartyl)-L-cysteine","type":"exact"},{"name":"N-beta-aspartylcysteine","type":"exact"},{"name":"N-isoaspartyl cysteine","type":"exact"}],"termid":"MOD:00221"}


id: MONDO:0019140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute ackee fruit intoxication (also referred to as Jamaican vomiting syndrome or sickness) is caused by the ingestion of unripe Blighia sapida fruits. It is a serious intoxication that is frequent in certain countries in the Caribbean and Western Africa. In contrast, it is rare in France and other Western countries. Intoxication leads to toxic hypoglycaemia and inhibition of neoglucogenesis. The hypoglycaemia is caused by the effect of hypoglycin A, which is found in the arils.","definition_xrefs":["Orphanet:73423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute ackee fruit intoxication","secondary_identifiers":["ICD9:988.2","MESH:C537562","SCTID:49434001","GARD:9299"],"synonyms":[{"name":"Jamaican vomiting sickness","type":"exact"},{"name":"Jamaican vomiting syndrome","type":"exact"},{"name":"ackee poisoning","type":"related"},{"name":"acute intoxication by Blighia sapida","type":"exact"}],"termid":"MONDO:0019140","xrefs":{"Monarch":{"xref_id":"0019140"}}}


id: GO:0010449
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The increase in size or mass of a root meristem, a population of undifferentiated cells in a plant root which maintains a continuous balance between the production of stem cells and the incorporation of their derivatives into the growth of the root.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meristem growth","termid":"GO:0035266"},{"relation_name":"part_of","term_name":"root development","termid":"GO:0048364"}],"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":"root meristem growth","termid":"GO:0010449"}


id: PBO:0088485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribonuclease III, endonuclease domain superfamily","termid":"PBO:0088485"}


id: PBO:0012290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteiasome complex subunit beta 1 Pre3 (predicted)","termid":"PBO:0012290"}


id: PBO:0036039
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-protein_interaction","termid":"PBO:0036039"}


id: PBO:0044291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome X open reading frame 66","termid":"PBO:0044291"}


id: PBO:0043817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copine 8","termid":"PBO:0043817"}


id: PR:Q9UTA0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC27E2.11c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTA0"],"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 C27E2.11c, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC27E2.11c","synonyms":[{"name":"Spom972h-SPAC27E2.11c","type":"exact"}],"termid":"PR:Q9UTA0"}


id: PBO:0087386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sterol transporter that transfers sterols between membranes; may regulate and coordinate formation of contact sites between organelles; localizes to ER-mitochondrial contact sites in a Tom70p- and Tom71p-dependent manner; mitochondrial localization requires GRAM domain; also localizes to ER-vacuole contact sites, in a Vac8p-dependent manner; has GRAM and StART-like (VASt) domains; one of six StART-like domain-containing proteins in yeast; conserved across eukaryotes","termid":"PBO:0087386"}


id: PBO:0109260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 120 member C","termid":"PBO:0109260"}


id: GO:0060552
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of fructose 1,6-bisphosphate metabolism. Fructose 1,6-bisphosphate metabolism is the chemical reactions and pathways involving fructose 1,6-bisphosphate, also known as FBP. The D enantiomer is a metabolic intermediate in glycolysis and gluconeogenesis.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of phosphate metabolic process","termid":"GO:0045937"},{"relation_name":"is_a","term_name":"regulation of fructose 1,6-bisphosphate metabolic process","termid":"GO:0060551"},{"relation_name":"positively_regulates","term_name":"fructose 1,6-bisphosphate metabolic process","termid":"GO:0030388"}],"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 fructose 1,6-bisphosphate metabolic process","termid":"GO:0060552"}


id: PBO:0060796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 2","termid":"PBO:0060796"}


id: PBO:0013466
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dimer x8","termid":"PBO:0013466"}


id: GO:0008268
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete receptor signaling protein tyrosine kinase signaling protein activity (obsolete GO:0008268)","synonyms":[{"name":"receptor signaling protein tyrosine kinase signaling protein activity","type":"exact"},{"name":"receptor signalling protein tyrosine kinase signalling protein activity","type":"exact"}],"termid":"GO:0008268"}


id: GO:1905611
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of mRNA cap binding.","definition_xrefs":["GOC:TermGenie","PMID:23409027","GOC:PARL","GOC:bc","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of mRNA cap binding (obsolete GO:1905611)","synonyms":[{"name":"down regulation of mRNA cap binding","type":"exact"},{"name":"down-regulation of mRNA cap binding","type":"exact"},{"name":"downregulation of mRNA cap binding","type":"exact"},{"name":"inhibition of mRNA cap binding","type":"narrow"}],"termid":"GO:1905611"}


id: GO:1900938
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of (Z)-nonadeca-1,14-diene metabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of olefin metabolic process","termid":"GO:1900908"},{"relation_name":"regulates","term_name":"(Z)-nonadeca-1,14-diene metabolic process","termid":"GO:1900878"}],"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 (Z)-nonadeca-1,14-diene metabolic process","synonyms":[{"name":"regulation of (Z)-nonadeca-1,14-diene metabolism","type":"exact"}],"termid":"GO:1900938"}


id: PATO:0001059
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001059 relative efficiency (obsolete PATO:0001059)","termid":"PATO:0001059"}


id: MONDO:0016420
data:
  {"annotated_genes":["SJAG_02885","SJAG_01356"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87890,87889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010819"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary macular dystrophy","termid":"MONDO:0020242"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01356":null,"SJAG_02885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"familial flecked retinopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:227786","ICD10CM:H35.5","icd11.foundation:979898273"],"synonyms":[{"name":"hereditary flecked retinopathy","type":"exact"}],"termid":"MONDO:0016420","terms_by_termid":{"MONDO:0010819":null},"xrefs":{"Monarch":{"xref_id":"0016420"}}}


id: PBO:0007714
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"possible frameshifted","termid":"PBO:0007714"}


id: PATO:0002467
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer resembling a thin narrow strip.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lathlike","termid":"PATO:0002467"}


id: MONDO:0018194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sex cord-stromal tumor of testis (obsolete MONDO:0018194)","termid":"MONDO:0018194","xrefs":{"Monarch":{"xref_id":"0018194"}}}


id: GO:0019302
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of D-ribose, (ribo-pentose).","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-ribose metabolic process","termid":"GO:0006014"},{"relation_name":"is_a","term_name":"pentose biosynthetic process","termid":"GO:0019322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"D-ribose biosynthetic process","synonyms":[{"name":"D-ribose anabolism","type":"exact"},{"name":"D-ribose biosynthesis","type":"exact"},{"name":"D-ribose formation","type":"exact"},{"name":"D-ribose synthesis","type":"exact"}],"termid":"GO:0019302"}


id: MONDO:0016191
data:
  {"annotated_genes":["SJAG_00185"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009709"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00185":null},"genotype_count":0,"is_obsolete":false,"name":"qualitative or quantitative defects of titin","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:20430","UMLS:C5680843","Orphanet:209053","MEDGEN:1843244"],"termid":"MONDO:0016191","terms_by_termid":{"MONDO:0009709":null},"xrefs":{"Monarch":{"xref_id":"0016191"}}}


id: MONDO:0010274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"testicular germ cell tumor","termid":"MONDO:0010108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testicular germ cell tumor 1","secondary_identifiers":["UMLS:C1846164","OMIM:300228","MEDGEN:337402","MESH:C564559"],"synonyms":[{"name":"TGCT1","type":"exact"},{"name":"testicular germ cell tumor","type":"broad"},{"name":"testicular germ cell tumor 1","type":"exact"},{"name":"testicular germ cell tumour","type":"broad"}],"termid":"MONDO:0010274","xrefs":{"Monarch":{"xref_id":"0010274"}}}


id: PR:O74746
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DnaJ homolog subfamily C member 8 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02702","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":"J domain-containing protein spf31 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1734.05c","secondary_identifiers":["UniProtKB:O74746"],"synonyms":[{"name":"Spom972h-DNAJC8","type":"exact"}],"termid":"PR:O74746"}


id: MONDO:0015533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-Langerhans cell histiocytosis","termid":"MONDO:0015531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"benign cephalic histiocytosis","secondary_identifiers":["MEDGEN:578000","UMLS:C0347403","Orphanet:157997","GARD:20019","SCTID:255192005","icd11.foundation:339468256","ICD9:216.8"],"termid":"MONDO:0015533","xrefs":{"Monarch":{"xref_id":"0015533"}}}


id: SO:0001834
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The constant region of an immunoglobulin polypeptide sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin_region","termid":"SO:0001832"}],"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":"C_region","synonyms":[{"name":"C region","type":"exact"}],"termid":"SO:0001834"}


id: PBO:0058886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 10523","termid":"PBO:0058886"}


id: MONDO:0012700
data:
  {"annotated_genes":["SJAG_01183"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86984],"is_not":false,"summary":null,"term":"MONDO:0012700"}]},"cv_name":"mondo","definition":"Distal renal tubular acidosis (dRTA) with anemia is a very rare form of distal renal tubular acidosis (dRTA) characterized by a defect in renal acidification and hereditary hemolytic anemia.","definition_xrefs":["Orphanet:93610"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hemolytic anemia","termid":"MONDO:0003689"},{"relation_name":"is_a","term_name":"distal renal tubular acidosis","termid":"MONDO:0015827"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01183":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280","MONDO:0005240"],"is_obsolete":false,"name":"renal tubular acidosis, distal, 4, with hemolytic anemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:12354","UMLS:C5436235","MEDGEN:1771439","OMIM:611590"],"synonyms":[{"name":"RTA, distal, autosomal recessive, with hemolytic Anaemia","type":"related"},{"name":"RTA, distal, autosomal recessive, with hemolytic Anemia","type":"related"},{"name":"dRTA with anaemia","type":"exact"},{"name":"dRTA with anemia","type":"exact"},{"name":"distal renal tubular acidosis 4 with hemolytic anaemia","type":"exact"},{"name":"distal renal tubular acidosis 4 with hemolytic anemia","type":"exact"},{"name":"distal renal tubular acidosis with anaemia","type":"exact"},{"name":"distal renal tubular acidosis with anemia","type":"exact"},{"name":"renal tubular acidosis, distal, with hemolytic anaemia","type":"related"},{"name":"renal tubular acidosis, distal, with hemolytic anemia","type":"related"},{"name":"renal tubular acidosis, distal, with normal Red cell morphology","type":"related"}],"termid":"MONDO:0012700","terms_by_termid":{"MONDO:0012700":null},"xrefs":{"Monarch":{"xref_id":"0012700"}}}


id: PBO:0064725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 61","termid":"PBO:0064725"}


id: PBO:0044257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X3-C motif chemokine receptor 1","termid":"PBO:0044257"}


id: PBO:0054537
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 1937","termid":"PBO:0054537"}


id: MOD:00678
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-proline residue to an hydroxylated L-proline.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydroxylated residue","termid":"MOD:00677"},{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxylated proline","synonyms":[{"name":"HyPro","type":"exact"}],"termid":"MOD:00678"}


id: GO:0019929
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The cross-linking of a cysteine residue to a glutamic acid residue to form 4-(S-L-cysteinyl)-L-glutamic acid.","definition_xrefs":["RESID:AA0315"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via 4-(S-L-cysteinyl)-L-glutamic acid (obsolete GO:0019929)","termid":"GO:0019929"}


id: PBO:0002470
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.6.1.19","termid":"PBO:0002470"}


id: GO:0033009
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small, vestigial nucleus found in some plastids that derive from a eukaryotic endosymbiont. Observed in chlorarachniophytes and cryptomonads, which acquired their plastids from a green and red alga respectively.","definition_xrefs":["PMID:16760254"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membrane-bounded organelle","termid":"GO:0043231"},{"relation_name":"part_of","term_name":"plastid","termid":"GO:0009536"}],"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:0005575","GO:0005737"],"is_obsolete":false,"name":"nucleomorph","secondary_identifiers":["Wikipedia:Nucleomorph"],"termid":"GO:0033009"}


id: PBO:0027813
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-lagging_chromosomes_during_meiosis_II","termid":"PBO:0027813"}


id: GO:0014074
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 purine-containing compound stimulus.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to purine-containing compound","synonyms":[{"name":"response to purine","type":"related"}],"termid":"GO:0014074"}


id: PBO:0011526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel subunit/aldo-keto reductase (predicted)","termid":"PBO:0011526"}


id: PR:000085721
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.2, initiator methionine removed K36-methylated form (Schizosaccharomyces pombe) whose methylation type is trimethylation. Example: UniProtKB:P09988, 2-136, Lys-37, MOD:00083.","definition_xrefs":["PomBase:VW","PMID:37459529","PRO:DAN"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hht2/Me3(K36)","pombase_gene_id":"SPBC8D2.04","synonyms":[{"name":"PRO_0000221366, Lys-37, MOD:00083","type":"related"},{"name":"PomBase_original_PRO_term_name: histone H3.2, initiator methionine removed K36-trimethylated form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hht2/InitMet-/K36Me3","type":"exact"},{"name":"UniProtKB:P09988, 2-136, Lys-37, MOD:00083","type":"related"},{"name":"hht2/Me3(K36)","type":"exact"}],"termid":"PR:000085721"}


id: PBO:0053251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LHX4 antisense RNA 1","termid":"PBO:0053251"}


id: SO:0000573
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region that can be transcribed into a ribosomal RNA (rRNA).","direct_ancestors":[{"relation_name":"is_a","term_name":"non_protein_coding","termid":"SO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA_encoding","synonyms":[{"name":"rRNA encoding","type":"exact"}],"termid":"SO:0000573"}


id: PBO:0041710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calmodulin 3","termid":"PBO:0041710"}


id: MONDO:0031240
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"panic disorder","termid":"MONDO:0005383"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial panic disorder","secondary_identifiers":["OMIMPS:167870"],"termid":"MONDO:0031240","xrefs":{"Monarch":{"xref_id":"0031240"}}}


id: MONDO:0700066
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any myopathy in which the cause of the disease is a variation in the FKRP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"qualitative or quantitative defects of FKRP","termid":"MONDO:0016156"},{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"},{"relation_name":"is_a","term_name":"disorder of protein O-glycosylation","termid":"MONDO:0017741"},{"relation_name":"is_a","term_name":"hereditary skeletal muscle disorder","termid":"MONDO:0700223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322","MONDO:0005336"],"is_obsolete":false,"name":"myopathy caused by variation in FKRP","synonyms":[{"name":"FKRP myopathy","type":"exact"},{"name":"FKRP-related myopathy","type":"exact"},{"name":"myopathy caused by mutation in FKRP","type":"exact"}],"termid":"MONDO:0700066","xrefs":{"Monarch":{"xref_id":"0700066"}}}


id: PBO:0049511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 18","termid":"PBO:0049511"}


id: PBO:0050743
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 5","termid":"PBO:0050743"}


id: PBO:0074401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 10","termid":"PBO:0074401"}


id: GO:0102809
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + delphinidin 3-O-beta-D-glucoside = H+ + delphinidin 3-O-sophoroside + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete delphinidin 3-O-glucoside 2''-O-glucosyltransferase activity (obsolete GO:0102809)","termid":"GO:0102809"}


id: MONDO:0007448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial dermographism is a condition also known as skin writing. When people who have dermatographia lightly scratch their skin, the scratches redden into a raised wheal similar to hives. Signs and symptoms of dermatographia include raised red lines, swelling, inflammation, hive-like welts and itching. Symptoms usually disappear within 30 minutes. The exact cause of this condition is unknown. Treatment may involve use of antihistamines if symptoms do not go away on their own.","definition_xrefs":["GARD:0009480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical urticaria","termid":"MONDO:0006599"}],"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":"familial dermatographia","secondary_identifiers":["ICD10CM:L50.3","DOID:743","ICD9:708.3","EFO:1000685","OMIM:125635","MEDGEN:342170","SCTID:7632005","UMLS:C1852145","MESH:C536612"],"synonyms":[{"name":"DDU","type":"related"},{"name":"Dermatographism, familial","type":"related"},{"name":"Dermodistortive urticaria","type":"related"},{"name":"VBU","type":"related"},{"name":"dermatographia","type":"related"},{"name":"dermatographic urticaria","type":"exact"},{"name":"dermo-distortive urticaria","type":"related"},{"name":"dermographism","type":"exact"},{"name":"dermographism, familial","type":"related"},{"name":"familial dermatographism","type":"related"},{"name":"familial dermographism","type":"related"},{"name":"vibratory angioedema","type":"related"},{"name":"vibratory urticaria","type":"related"}],"termid":"MONDO:0007448","xrefs":{"Monarch":{"xref_id":"0007448"}}}


id: MONDO:0016827
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myopathy-growth delay-intellectual disability-hypospadias syndrome","secondary_identifiers":["Orphanet:2601"],"termid":"MONDO:0016827","xrefs":{"Monarch":{"xref_id":"0016827"}}}


id: MONDO:0859166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"visceral leiomyopathy, African degenerative","secondary_identifiers":["UMLS:C5443983","OMIM:619400","MEDGEN:1781444"],"termid":"MONDO:0859166","xrefs":{"Monarch":{"xref_id":"0859166"}}}


id: PBO:0075975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal transducer and activator of transcription 1","termid":"PBO:0075975"}


id: PBO:0049982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIKESHI pseudogene 3","termid":"PBO:0049982"}


id: PBO:0004735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylethanolamine N-methyltransferase Cho2","termid":"PBO:0004735"}


id: MONDO:0003313
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare sarcoma that arises from the vagina. This category includes low grade endometrioid stromal sarcoma and undifferentiated vaginal sarcoma.","definition_xrefs":["NCIT:C40270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vagina sarcoma","termid":"MONDO:0002140"},{"relation_name":"is_a","term_name":"endometrioid stromal and related neoplasms of the vagina","termid":"MONDO:0003314"},{"relation_name":"is_a","term_name":"endometrioid stromal sarcoma","termid":"MONDO:0006745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"endometrioid stromal sarcoma of the vagina","secondary_identifiers":["DOID:5170","UMLS:C3642329","MEDGEN:770969"],"synonyms":[{"name":"endometrioid stromal sarcoma of the vagina","type":"exact"},{"name":"endometrioid stromal sarcoma of vagina","type":"exact"},{"name":"vagina endometrioid stromal sarcoma","type":"exact"},{"name":"vaginal endometrial stromal sarcoma","type":"related"}],"termid":"MONDO:0003313","xrefs":{"Monarch":{"xref_id":"0003313"}}}


id: PBO:0062857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otopetrin 2","termid":"PBO:0062857"}


id: PBO:0082209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-1,3-mannosyltransferase; integral membrane glycoprotein of the Golgi complex, required for addition of alpha1,3-mannose linkages to N-linked and O-linked oligosaccharides, one of five S. cerevisiae proteins of the MNN1 family","termid":"PBO:0082209"}


id: GO:0010379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phaseic acid (PA), a catabolite of the plant hormone abscisic acid (ABA).","definition_xrefs":["MetaCyc:PWY-5271"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpenoid biosynthetic process","termid":"GO:0016106"},{"relation_name":"is_a","term_name":"apocarotenoid biosynthetic process","termid":"GO:0043289"},{"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:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"phaseic acid biosynthetic process","termid":"GO:0010379"}


id: MONDO:0100548
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neurological disorder in which the cause of the disease is a mutation in the SERAC1 gene.","definition_xrefs":["PMID:28916646","PMID:37090937","PMID:29686941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SERAC1-related neurological disorder","termid":"MONDO:0100548","xrefs":{"Monarch":{"xref_id":"0100548"}}}


id: PBO:0044066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystatin 9-like pseudogene 2","termid":"PBO:0044066"}


id: GO:2000056
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of Wnt signaling pathway involved in digestive tract morphogenesis.","definition_xrefs":["GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of Wnt signaling pathway involved in digestive tract morphogenesis (obsolete GO:2000056)","synonyms":[{"name":"regulation of Wnt receptor signaling pathway involved in digestive tract morphogenesis","type":"exact"},{"name":"regulation of Wnt receptor signalling pathway involved in digestive tract morphogenesis","type":"exact"},{"name":"regulation of Wnt-activated signaling pathway involved in digestive tract morphogenesis","type":"related"}],"termid":"GO:2000056"}


id: GO:0004591
data:
  {"annotated_genes":["SJAG_02464"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71968],"is_not":false,"summary":null,"term":"GO:0004591"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: N(6)-[(R)-lipoyl]-L-lysyl-[dihydrolipoyllysine-residue succinyltransferase] + 2-oxoglutarate + H+ = N(6)-[(R)-S(8)-succinyldihydrolipoyl]-L-lysyl-[dihydrolipoyllysine-residue succinyltransferase] + CO2.","definition_xrefs":["RHEA:12188"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor","termid":"GO:0016624"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02464":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"oxoglutarate dehydrogenase (succinyl-transferring) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:2OXOGLUTDECARB-RXN","EC:1.2.4.2","Reactome:R-HSA-71401"],"synonyms":[{"name":"2-ketoglutarate dehydrogenase activity","type":"related"},{"name":"2-oxoglutarate dehydrogenase activity","type":"related"},{"name":"2-oxoglutarate: lipoate oxidoreductase activity","type":"related"},{"name":"2-oxoglutarate:dihydrolipoyllysine-residue succinyltransferase-lipoyllysine 2-oxidoreductase (decarboxylating, acceptor-succinylating)","type":"related"},{"name":"2-oxoglutarate:lipoamide 2-oxidoreductase (decarboxylating and acceptor-succinylating) activity","type":"related"},{"name":"AKGDH activity","type":"related"},{"name":"OGDC activity","type":"related"},{"name":"alpha-ketoglutarate dehydrogenase activity","type":"related"},{"name":"alpha-ketoglutaric acid dehydrogenase activity","type":"related"},{"name":"alpha-ketoglutaric dehydrogenase activity","type":"related"},{"name":"alpha-oxoglutarate dehydrogenase activity","type":"related"},{"name":"ketoglutaric dehydrogenase activity","type":"related"},{"name":"oxoglutarate decarboxylase activity","type":"related"},{"name":"oxoglutarate dehydrogenase (lipoamide) activity","type":"exact"},{"name":"oxoglutarate dehydrogenase activity","type":"related"}],"termid":"GO:0004591","terms_by_termid":{"GO:0004591":null}}


id: GO:0051450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of myoblasts, resulting in the expansion of a myoblast cell population. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["GOC:ai","GOC:mtg_muscle","CL:0000056"],"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":"myoblast proliferation","termid":"GO:0051450"}


id: GO:1903500
data:
  {"annotated_genes":["SJAG_02838","SJAG_01787","SJAG_00845","SJAG_02592","SJAG_02392","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92579,96181,97668,104187,105514,112614],"is_not":false,"summary":null,"term":"GO:1903500"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mitotic actomyosin contractile ring assembly.","definition_xrefs":["GOC:al","GO_REF:0000058","GOC:mtg_cell_cycle","PMID:18256290","GOC:vw","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mitotic cytokinetic process","termid":"GO:1903437"},{"relation_name":"is_a","term_name":"regulation of mitotic actomyosin contractile ring assembly","termid":"GO:1903499"},{"relation_name":"is_a","term_name":"negative regulation of cytokinesis, actomyosin contractile ring assembly","termid":"GO:2000432"},{"relation_name":"negatively_regulates","term_name":"mitotic actomyosin contractile ring assembly","termid":"GO:1903475"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00845":null,"SJAG_01787":null,"SJAG_02392":null,"SJAG_02592":null,"SJAG_02838":null,"SJAG_03048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0000281"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"negatively_regulates","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0000281"}],"interesting_parent_ids":["GO:0000281","GO:0008150","GO:0007010","GO:0030036","GO:0007049","GO:0044085"],"is_obsolete":false,"name":"negative regulation of mitotic actomyosin contractile ring assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of actomyosin contractile ring assembly involved in cytokinesis after mitosis","type":"exact"},{"name":"down regulation of contractile ring assembly involved in mitotic cytokinesis","type":"exact"},{"name":"down regulation of cytokinesis, actomyosin contractile ring assembly involved in mitotic cytokinesis","type":"exact"},{"name":"down regulation of mitotic actomyosin contractile ring assembly","type":"exact"},{"name":"down-regulation of actomyosin contractile ring assembly involved in cytokinesis after mitosis","type":"exact"},{"name":"down-regulation of contractile ring assembly involved in mitotic cytokinesis","type":"exact"},{"name":"down-regulation of cytokinesis, actomyosin contractile ring assembly involved in mitotic cytokinesis","type":"exact"},{"name":"down-regulation of mitotic actomyosin contractile ring assembly","type":"exact"},{"name":"downregulation of actomyosin contractile ring assembly involved in cytokinesis after mitosis","type":"exact"},{"name":"downregulation of contractile ring assembly involved in mitotic cytokinesis","type":"exact"},{"name":"downregulation of cytokinesis, actomyosin contractile ring assembly involved in mitotic cytokinesis","type":"exact"},{"name":"downregulation of mitotic actomyosin contractile ring assembly","type":"exact"},{"name":"inhibition of actomyosin contractile ring assembly involved in cytokinesis after mitosis","type":"narrow"},{"name":"inhibition of contractile ring assembly involved in mitotic cytokinesis","type":"narrow"},{"name":"inhibition of cytokinesis, actomyosin contractile ring assembly involved in mitotic cytokinesis","type":"narrow"},{"name":"inhibition of mitotic actomyosin contractile ring assembly","type":"narrow"},{"name":"negative regulation of actomyosin contractile ring assembly involved in cytokinesis after mitosis","type":"exact"},{"name":"negative regulation of contractile ring assembly involved in mitotic cytokinesis","type":"exact"},{"name":"negative regulation of cytokinesis, actomyosin contractile ring assembly involved in mitotic cytokinesis","type":"exact"},{"name":"negative regulation of mitotic cytokinesis, actomyosin contractile ring assembly","type":"exact"}],"termid":"GO:1903500","terms_by_termid":{"GO:1903500":null}}


id: PBO:0031227
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_chromatin_silencing_at_rDNA","termid":"PBO:0031227"}


id: GO:1902923
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of poly(3-hydroxyvalerate).","definition_xrefs":["GOC:mengo_curators","GO_REF:0000068","GOC:TermGenie","PMID:21705209"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poly(hydroxyvalerate) biosynthetic process","termid":"GO:1902921"},{"relation_name":"is_a","term_name":"poly(3-hydroxyvalerate) metabolic process","termid":"GO:1902922"}],"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":"poly(3-hydroxyvalerate) biosynthetic process","synonyms":[{"name":"poly(3-hydroxyvalerate) anabolism","type":"exact"},{"name":"poly(3-hydroxyvalerate) biosynthesis","type":"exact"},{"name":"poly(3-hydroxyvalerate) formation","type":"exact"},{"name":"poly(3-hydroxyvalerate) synthesis","type":"exact"}],"termid":"GO:1902923"}


id: MONDO:0957978
data:
  {"annotated_genes":["SJAG_02007"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87844],"is_not":false,"summary":null,"term":"MONDO:0957978"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary optic atrophy","termid":"MONDO:0043878"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02007":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"optic atrophy 16","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5882723","MEDGEN:1851641","OMIM:620629"],"termid":"MONDO:0957978","terms_by_termid":{"MONDO:0957978":null},"xrefs":{"Monarch":{"xref_id":"0957978"}}}


id: GO:0140725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces or removes the toxicity of free heme. These include transport of heme away from sensitive areas and to compartments or complexes whose purpose is sequestration of heme.","definition_xrefs":["PMID:26741528","PMID:32983129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detoxification","termid":"GO:0098754"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"detoxification of free heme","synonyms":[{"name":"free heme detoxification","type":"exact"}],"termid":"GO:0140725"}


id: PBO:0074346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 pseudogene 5","termid":"PBO:0074346"}


id: GO:0097291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A renal system process in which phosphate ions are taken up from the collecting ducts and proximal and distal loops of the nephron. In non-mammalian species, absorption may occur in related structures.","definition_xrefs":["GOC:lb","PMID:22506049","PMID:18784102"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal absorption","termid":"GO:0070293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal phosphate ion absorption","synonyms":[{"name":"renal phosphate absorption","type":"exact"}],"termid":"GO:0097291"}


id: PBO:0090837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA (guanine-N7-)-methyltransferase catalytic subunit Trm8","termid":"PBO:0090837"}


id: _global:existence_ends_during_or_before
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"x existence ends during or before y if and only if the time point at which x ends is before or equivalent to the time point at which y ends.","direct_ancestors":[{"relation_name":"is_a","term_name":"relation_between_physical_entity_and_a_process_or_stage","termid":"_global:relation_between_physical_entity_and_a_process_or_stage"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"existence_ends_during_or_before","secondary_identifiers":["RO:0002497"],"termid":"_global:existence_ends_during_or_before"}


id: MOD:01789
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an N-terminal L-phenylalanine residue to phenylalanine immonium ion.","definition_xrefs":["PubMed:18688235","PubMed:17074506"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-phenylalanine residue","termid":"MOD:00914"},{"relation_name":"is_a","term_name":"residue reporter fragment","termid":"MOD:01527"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phenylalanine immonium ion","synonyms":[{"name":"2-phenylethaniminium","type":"exact"}],"termid":"MOD:01789"}


id: MONDO:0020069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Chronic form of encephalitis.","definition_xrefs":["MONDO:patterns/chronic"],"gene_count":0,"genotype_count":0,"name":"obsolete chronic encephalitis (obsolete MONDO:0020069)","secondary_identifiers":["Orphanet:98255"],"synonyms":[{"name":"encephalitis, chronic","type":"exact"}],"termid":"MONDO:0020069","xrefs":{"Monarch":{"xref_id":"0020069"}}}


id: MONDO:0024864
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"posterior uveal melanoma","termid":"MONDO:0003927"}],"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":"medium/large size posterior uveal melanoma","secondary_identifiers":["MEDGEN:124525","NCIT:C9090","UMLS:C0278868"],"synonyms":[{"name":"medium/large size posterior uveal melanoma","type":"exact"}],"termid":"MONDO:0024864","xrefs":{"Monarch":{"xref_id":"0024864"}}}


id: PBO:0073178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenoprotein K","termid":"PBO:0073178"}


id: SO:0001593
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant which causes a disruption of the translational reading frame, by shifting two bases forward.","direct_ancestors":[{"relation_name":"is_a","term_name":"frameshift_variant","termid":"SO:0001589"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minus_2_frameshift_variant","synonyms":[{"name":"-2 frameshift variant","type":"exact"},{"name":"minus 2 frameshift variant","type":"exact"}],"termid":"SO:0001593"}


id: MONDO:0009897
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Adult polyglucosan body disease (APBD) is a glycogen storage disease of adults characterized by progressive upper and lower motor neuron dysfunction, progressive neurogenic bladder and cognitive difficulties that can lead to dementia.","definition_xrefs":["Orphanet:206583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycogen storage disease due to glycogen branching enzyme deficiency","termid":"MONDO:0009292"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"adult polyglucosan body disease","secondary_identifiers":["NORD:1591","GARD:108","MEDGEN:342338","NANDO:2201163","UMLS:C1849722","OMIM:263570","MESH:C564878","SCTID:721099001"],"synonyms":[{"name":"APBD","type":"exact"},{"name":"APBN","type":"related"},{"name":"polyglucosan body disease, adult","type":"related"},{"name":"polyglucosan body disease, adult form","type":"related"},{"name":"polyglucosan body neuropathy, adult form","type":"related"}],"termid":"MONDO:0009897","xrefs":{"Monarch":{"xref_id":"0009897"}}}


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


id: MOD:00114
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to L-cysteine methyl ester.","definition_xrefs":["PubMed:11875433","PubMed:1872463","Unimod:34#C-term","RESID:AA0105"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monomethylated L-cysteine","termid":"MOD:01682"},{"relation_name":"is_a","term_name":"alpha-carboxyl methylated residue","termid":"MOD:01689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"},{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00905","MOD:00427"],"is_obsolete":false,"name":"L-cysteine methyl ester","synonyms":[{"name":"2-amino-3-mercaptopropanoic methyl ester","type":"exact"},{"name":"2-amino-3-sulfanylpropanoic methyl ester","type":"exact"},{"name":"L-cysteine methyl ester","type":"exact"},{"name":"MOD_RES Cysteine methyl ester","type":"exact"},{"name":"Methyl","type":"related"},{"name":"Methylation","type":"related"},{"name":"OMeCys","type":"exact"},{"name":"mecysteine","type":"exact"},{"name":"methyl (2R)-2-amino-3-sulfanylpropanoate","type":"exact"},{"name":"methyl L-cysteinate","type":"exact"},{"name":"methyl esterified L-cysteine","type":"exact"}],"termid":"MOD:00114"}


id: FYPO:0008332
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 addition of one or more uridylyl residues to the poly(A) tails of mRNA molecules occurs to a lower extent than normal.","definition_xrefs":["PMID:39333464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA modification","termid":"FYPO:0000372"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"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:0000294","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased mRNA poly(A) tail uridylation","termid":"FYPO:0008332"}


id: GO:0072765
data:
  {"annotated_genes":["SJAG_03683","SJAG_05196","SJAG_02761","SJAG_02624","SJAG_02814","SJAG_00794","SJAG_02737","SJAG_01613","SJAG_02299","SJAG_04076","SJAG_01745","SJAG_00727","SJAG_01805","SJAG_03540","SJAG_03126"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098653"},{"annotations":[93154,91408,104639,118806,111809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072766"},{"annotations":[110983,117784,104255,66730,95609,97129,70177,102198,101034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990571"}]},"cv_name":"biological_process","definition":"A cellular localization process in which a centromere/kinetochore is transported to, or maintained in, a specific location.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex localization","termid":"GO:0031503"},{"relation_name":"is_a","term_name":"organelle localization","termid":"GO:0051640"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00727":null,"SJAG_00794":null,"SJAG_01613":null,"SJAG_01745":null,"SJAG_01805":null,"SJAG_02299":null,"SJAG_02624":null,"SJAG_02737":null,"SJAG_02761":null,"SJAG_02814":null,"SJAG_03126":null,"SJAG_03540":null,"SJAG_03683":null,"SJAG_04076":null,"SJAG_05196":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"centromere localization","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"establishment and maintenance of kinetochore localization","type":"exact"},{"name":"kinetochore localisation","type":"exact"},{"name":"kinetochore localization","type":"exact"}],"termid":"GO:0072765","terms_by_termid":{"GO:0072766":null,"GO:0098653":null,"GO:1990571":null}}


id: PBO:0090010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L22","termid":"PBO:0090010"}


id: GO:0042598
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any of the small, heterogeneous, artifactual, vesicular particles that are formed when some cells are homogenized.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete vesicular fraction (obsolete GO:0042598)","synonyms":[{"name":"vesicular fraction","type":"exact"}],"termid":"GO:0042598"}


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


id: SO:0000255
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding a small ribosomal subunit RNA.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA_primary_transcript","termid":"SO:0000209"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA_small_subunit_primary_transcript","synonyms":[{"name":"rRNA small subunit primary transcript","type":"exact"}],"termid":"SO:0000255"}


id: PBO:0069748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1029, pseudogene","termid":"PBO:0069748"}


id: PBO:0063873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol glycan anchor biosynthesis class C pseudogene 2","termid":"PBO:0063873"}


id: PBO:0027903
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_degradation_during_mitotic_G1_phase","termid":"PBO:0027903"}


id: PATO:0000249
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000249 righting reflex (obsolete PATO:0000249)","termid":"PATO:0000249"}


id: MONDO:0002138
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A allergic contact dermatitis that involves the eyelid.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"noninfectious dermatoses of eyelid","termid":"MONDO:0002137"},{"relation_name":"is_a","term_name":"eye allergy","termid":"MONDO:0005551"},{"relation_name":"is_a","term_name":"allergic contact dermatitis","termid":"MONDO:0006525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"allergic contact dermatitis of eyelid","secondary_identifiers":["ICD9:692.9","ICD9:373.32","MEDGEN:509833","UMLS:C0155178","SCTID:402249007","DOID:1895"],"synonyms":[{"name":"contact and allergic dermatitis of eyelid","type":"exact"},{"name":"eyelid allergic contact dermatitis","type":"exact"}],"termid":"MONDO:0002138","xrefs":{"Monarch":{"xref_id":"0002138"}}}


id: FYPO:0000164
data:
  {"alleles_by_uniquename":{"SJAG_02252:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02252","name":"ace2delta","uniquename":"SJAG_02252:allele-1"},"SJAG_03143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03143","name":"sep1delta","uniquename":"SJAG_03143:allele-1"},"SJAG_03444:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03444","name":"agn1delta","uniquename":"SJAG_03444:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001971"},{"annotations":[121377,121376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006557"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which cell separation after cytokinesis is abnormal. Cell separation is the process of physically separating progeny cells after cytokinesis is complete, and involves enzymatic digestion of septum components.","definition_xrefs":["GO:0000920","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell division during vegetative growth","termid":"FYPO:0000186"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02252":null,"SJAG_03143":null,"SJAG_03444":null},"genotype_count":3,"genotypes_by_uniquename":{"ace2delta":{"display_name":"ace2delta","display_uniquename":"ace2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02252:allele-1","expression":"Null"}]}]},"agn1delta":{"display_name":"agn1delta","display_uniquename":"agn1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03444:allele-1","expression":"Null"}]}]},"sep1delta":{"display_name":"sep1delta","display_uniquename":"sep1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03143:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal cell separation after cytokinesis","references_by_uniquename":{"PMID:22300943":null,"PMID:24699070":null},"single_locus_annotated_genes":["SJAG_03143","SJAG_03444","SJAG_02252"],"single_locus_genotype_uniquenames":["agn1delta","sep1delta","ace2delta"],"synonyms":[{"name":"abnormal cell separation after cytokinesis during mitotic cell cycle","type":"related"},{"name":"abnormal cell separation after cytokinesis during vegetative growth","type":"exact"},{"name":"abnormal mitotic cytokinetic cell separation","type":"exact"},{"name":"abnormal septum digestion after cytokinesis","type":"exact"}],"termid":"FYPO:0000164","terms_by_termid":{"FYECO:0000137":null,"FYPO:0001971":null,"FYPO:0006557":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PBO:0075438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPANX family member N3","termid":"PBO:0075438"}


id: PBO:0073349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SERPINB9 antisense RNA 1","termid":"PBO:0073349"}


id: PBO:0048853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosamine (N-acetyl)-6-sulfatase","termid":"PBO:0048853"}


id: PBO:0084102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Guanyl-nucleotide exchange factor for the small G-protein Sec4p; essential for post-Golgi vesicle transport and for autophagy; associates with the exocyst, via exocyst subunit Sec15p, on secretory vesicles","termid":"PBO:0084102"}


id: PBO:0084782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial phenylalanyl-tRNA synthetase; active as a monomer, unlike the cytoplasmic subunit which is active as a dimer complexed to a beta subunit dimer; similar to the alpha subunit of E. coli phenylalanyl-tRNA synthetase","termid":"PBO:0084782"}


id: PBO:0076366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trace amine associated receptor 3, pseudogene","termid":"PBO:0076366"}


id: GO:0044031
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism adds a phosphate group to a protein of the host 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 modification by symbiont of host protein by phosphorylation (obsolete GO:0044031)","termid":"GO:0044031"}


id: MONDO:0020629
data:
  {"annotated_genes":["SJAG_04816","SJAG_03898"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008876"},{"annotations":[88205],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020628"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03898":null,"SJAG_04816":null},"genotype_count":0,"is_obsolete":false,"name":"microcephaly, growth restriction and increased sister chromatid exchange","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:210900"],"synonyms":[{"name":"MGRISCE","type":"exact"}],"termid":"MONDO:0020629","terms_by_termid":{"MONDO:0008876":null,"MONDO:0020628":null},"xrefs":{"Monarch":{"xref_id":"0020629"}}}


id: PBO:0073748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 2 member 4","termid":"PBO:0073748"}


id: MONDO:1010236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syringomyelia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syringomyelia, non-human animal","secondary_identifiers":["OMIA:000965"],"termid":"MONDO:1010236","xrefs":{"Monarch":{"xref_id":"1010236"}}}


id: MONDO:0003820
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ovarian teratoma which may be cystic, composed entirely of well differentiated, adult-type tissues, without evidence of fetal-type tissues.","definition_xrefs":["NCIT:C8112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mature teratoma","termid":"MONDO:0003517"},{"relation_name":"is_a","term_name":"ovarian biphasic or triphasic teratoma","termid":"MONDO:0003821"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mature ovarian teratoma","secondary_identifiers":["DOID:6231","UMLS:C1334637","ONCOTREE:OMT","MEDGEN:233672"],"synonyms":[{"name":"mature ovarian teratoma","type":"exact"},{"name":"mature teratoma","type":"related"},{"name":"mature teratoma of ovary","type":"exact"},{"name":"mature teratoma of the ovary","type":"related"},{"name":"ovary mature teratoma","type":"exact"}],"termid":"MONDO:0003820","xrefs":{"Monarch":{"xref_id":"0003820"}}}


id: PBO:0027078
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_plasma_membrane,_with_protein_mislocalized_to_cytoplasm,_during_glucose_starvation","termid":"PBO:0027078"}


id: MONDO:0025484
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acquired defect of cellular immunity that occurs naturally in macaques infected with srv serotypes, experimentally in monkeys inoculated with srv or mason-pfizer monkey virus; (mpmv), or in monkeys infected with simian immunodeficiency virus.","definition_xrefs":["MESH:D016097"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monkey disease","termid":"MONDO:0025102"},{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"simian acquired immunodeficiency syndrome","synonyms":[{"name":"AIDS, Simian","type":"related"},{"name":"AIDSs, Simian","type":"related"},{"name":"SAIDS","type":"related"},{"name":"Simian AIDS","type":"related"},{"name":"Simian AIDSs","type":"related"},{"name":"Simian acquired immune deficiency syndrome","type":"related"},{"name":"Simian acquired immuno deficiency syndrome","type":"related"},{"name":"Simian acquired immuno-deficiency syndrome","type":"related"},{"name":"Simian immunodeficiency virus caused monkey disease","type":"exact"},{"name":"Simian immunodeficiency virus monkey disease","type":"exact"}],"termid":"MONDO:0025484","xrefs":{"Monarch":{"xref_id":"0025484"}}}


id: PBO:0062959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A) binding protein cytoplasmic 1 pseudogene 2","termid":"PBO:0062959"}


id: PBO:0028969
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_superoxide_dismutase_activity","termid":"PBO:0028969"}


id: FYPO:0003205
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A septation phenotype observed in the vegetative growth phase of the life cycle in which a cell forms a primary septum that is thinner than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased septum thickness","termid":"FYPO:0006900"},{"relation_name":"output_of","term_name":"abnormal primary cell septum biogenesis","termid":"FYPO:0003890"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000032"],"is_obsolete":false,"name":"decreased primary cell septum thickness","synonyms":[{"name":"decreased primary cell septum thickness during mitotic cell cycle","type":"related"},{"name":"decreased primary cell septum thickness during vegetative growth","type":"exact"},{"name":"decreased primary septum thickness","type":"exact"},{"name":"reduced primary cell septum thickness","type":"exact"},{"name":"thin primary septum","type":"exact"}],"termid":"FYPO:0003205"}


id: PR:Q9USK5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A TIP41-like protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04568","PANTHER:PTHR21021:SF16","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":"type 2A phosphatase activator tip41 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4B3.16","secondary_identifiers":["UniProtKB:Q9USK5"],"synonyms":[{"name":"PP2A phosphatase activator tip41 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-TIPRL","type":"exact"}],"termid":"PR:Q9USK5"}


id: PBO:0031781
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_endocytosis_during_vegetative_growth","termid":"PBO:0031781"}


id: PBO:0065933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rac family small GTPase 1 pseudogene 7","termid":"PBO:0065933"}


id: PBO:0055231
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 2658","termid":"PBO:0055231"}


id: GO:0004867
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of a serine-type endopeptidase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endopeptidase inhibitor activity","termid":"GO:0004866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0030234","GO:0004857","GO:0140678","GO:0003674","GO:0098772"],"is_obsolete":false,"name":"serine-type endopeptidase inhibitor activity","secondary_identifiers":["Reactome:R-HSA-158893","Reactome:R-HSA-159001","Reactome:R-HSA-159005","Reactome:R-HSA-158795","Reactome:R-HSA-158800"],"synonyms":[{"name":"serine protease inhibitor activity","type":"narrow"},{"name":"serine proteinase inhibitor activity","type":"narrow"},{"name":"serpin activity","type":"narrow"}],"termid":"GO:0004867"}


id: FYPO:0002433
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which all cells in the population are inviable and have abnormal cell shape, in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable vegetative cell population with abnormal cell shape (obsolete FYPO:0002433)","synonyms":[{"name":"inviable, abnormally shaped vegetative cell population","type":"exact"},{"name":"lethal; vegetative cell population with abnormal cell shape","type":"exact"}],"termid":"FYPO:0002433"}


id: PR:O94704
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- iec3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94704"],"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":"INO80 complex subunit 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1259.04","synonyms":[{"name":"Spom972h-iec3","type":"exact"}],"termid":"PR:O94704"}


id: GO:0014073
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 tropane stimulus. Tropane is a nitrogenous bicyclic organic compound mainly known for a group of alkaloids derived from it (called tropane alkaloids), which include, among others, atropine and cocaine.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to alkaloid","termid":"GO:0043279"}],"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 tropane","termid":"GO:0014073"}


id: SO:0002112
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A protein coding transcript containing a retained intron.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein_coding_primary_transcript","termid":"SO:0000120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coding_transcript_with_retained_intron","synonyms":[{"name":"mRNA with retained intron","type":"related"}],"termid":"SO:0002112"}


id: PBO:0048769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glia maturation factor gamma","termid":"PBO:0048769"}


id: MONDO:0021148
data:
  {"annotated_genes":["SJAG_02748","SJAG_04394","SJAG_01156","SJAG_01419","SJAG_04206","SJAG_02426"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89078,86811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011962"},{"annotations":[88936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032747"},{"annotations":[88287,88286,88288],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008170"}]},"cv_name":"mondo","definition":"A benign, precancerous, or malignant neoplasm that affects the female reproductive system. Representative examples include uterine corpus leiomyoma, endocervical polyp, ovarian carcinoma, cervical carcinoma, and endometrial carcinoma.","definition_xrefs":["NCIT:C3053"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"},{"relation_name":"is_a","term_name":"reproductive system neoplasm","termid":"MONDO:0006054"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01156":null,"SJAG_01419":null,"SJAG_02426":null,"SJAG_02748":null,"SJAG_04206":null,"SJAG_04394":null},"genotype_count":0,"is_obsolete":false,"name":"female reproductive system neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:9004","MESH:D005833","UMLS:C0017416"],"synonyms":[{"name":"female reproductive organ neoplasm (disease)","type":"exact"},{"name":"female reproductive organ tumor","type":"exact"},{"name":"female reproductive organ tumour","type":"exact"},{"name":"female reproductive system neoplasm","type":"exact"},{"name":"female reproductive system neoplasm (disease)","type":"exact"},{"name":"female reproductive system tumor","type":"exact"},{"name":"female reproductive system tumour","type":"exact"},{"name":"gynecologic neoplasm","type":"exact"},{"name":"gynecologic tumor","type":"exact"},{"name":"gynecologic tumour","type":"exact"},{"name":"neoplasm of female reproductive organ","type":"exact"},{"name":"neoplasm of female reproductive system","type":"exact"},{"name":"neoplasm of the female reproductive system","type":"exact"},{"name":"tumor of female reproductive system","type":"exact"},{"name":"tumor of the female reproductive system","type":"exact"},{"name":"tumour of female reproductive system","type":"exact"},{"name":"tumour of the female reproductive system","type":"exact"}],"termid":"MONDO:0021148","terms_by_termid":{"MONDO:0008170":null,"MONDO:0011962":null,"MONDO:0032747":null},"xrefs":{"Monarch":{"xref_id":"0021148"}}}


id: PBO:0082875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Covalently linked cell wall glycoprotein; present in the inner layer of the cell wall","termid":"PBO:0082875"}


id: MONDO:0968991
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary central precocious puberty in male","termid":"MONDO:0958356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-genetic central precocious puberty in male","secondary_identifiers":["MEDGEN:1853153","UMLS:C5816759","Orphanet:650102"],"termid":"MONDO:0968991","xrefs":{"Monarch":{"xref_id":"0968991"}}}


id: GO:0098761
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-7 stimulus.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"},{"relation_name":"is_a","term_name":"response to interleukin-7","termid":"GO:0098760"}],"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 interleukin-7","synonyms":[{"name":"cellular response to IL-7","type":"exact"}],"termid":"GO:0098761"}


id: GO:0033282
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex of protein C inhibitor (SERPINA5) and acrosin; formation of the complex inhibits the protease activity of acrosin.","definition_xrefs":["PMID:11120760","GOC:pr","PMID:7521127"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine protease inhibitor complex","termid":"GO:0097180"},{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"acrosomal membrane","termid":"GO:0002080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0031410","GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"protein C inhibitor-acrosin complex","synonyms":[{"name":"PCI-ACR complex","type":"exact"},{"name":"PCI-acrosin complex","type":"exact"},{"name":"SERPINA5-acrosin complex","type":"exact"},{"name":"plasma serine protease inhibitor-acrosin complex","type":"exact"},{"name":"serpin A5-acrosin complex","type":"exact"}],"termid":"GO:0033282"}


id: PBO:0044705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDX5 pseudogene 1","termid":"PBO:0044705"}


id: PBO:0059110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MOS proto-oncogene, serine/threonine kinase","termid":"PBO:0059110"}


id: GO:1990302
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ubiquitin ligase complex consisting of Bre1 and Rad6 that mediates monoubiquitination of histone H2B to form H2BK123ub1. H2BK123ub1 gives a specific tag for epigenetic transcriptional activation, elongation by RNA polymerase II, telomeric silencing, and is also a prerequisite for H3K4me and H3K79me formation. It thereby plays a central role in histone code and gene regulation. It also modulates the formation of double-strand breaks during meiosis.","definition_xrefs":["PMID:19531475","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"},{"relation_name":"part_of","term_name":"intracellular anatomical structure","termid":"GO:0005622"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Bre1-Rad6 ubiquitin ligase complex","synonyms":[{"name":"Bre1-Rad6 complex","type":"exact"}],"termid":"GO:1990302"}


id: MONDO:0001154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A spotted fever that has material basis in Rickettsia sibirica, which is transmitted by ticks (Dermacentor nuttalli, Dermacentor marginatus and Haemaphysalis concinna). The infection has symptom fever, has symptom eschar, has symptom regional adenopathy, and has symptom maculopapular rash.","definition_xrefs":["DOID:10921"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spotted fever","termid":"MONDO:0001195"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Siberian tick typhus","secondary_identifiers":["ICD9:082.2","SCTID:186781003","ICD10CM:A77.2","MEDGEN:639822","UMLS:C0549160"],"synonyms":[{"name":"Manchurian typhus","type":"exact"},{"name":"North Asian tick fever","type":"exact"},{"name":"North Asian tick fever (disorder) [ambiguous]","type":"exact"},{"name":"North Asian tick typhus","type":"exact"},{"name":"Rickettsia sibirica spotted fever","type":"exact"}],"termid":"MONDO:0001154","xrefs":{"Monarch":{"xref_id":"0001154"}}}


id: PBO:0002816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone lysine methyltransferase Set3","termid":"PBO:0002816"}


id: PBO:0055845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat, Ig-like and transmembrane domains 1","termid":"PBO:0055845"}


id: FYPO:0001190
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 one or more enzymes that degrades cell wall polysaccharides. Cells stop growing (and may die) at a concentration of such enzymes 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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0000139","FYPO:0005447","FYPO:0001985","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to cell wall-degrading enzymes","secondary_identifiers":["FYPO:0001191"],"synonyms":[{"name":"hypersensitive to cell wall-degrading enzymes","type":"exact"},{"name":"sensitive to Lyticase","type":"narrow"},{"name":"sensitive to Novozyme 234","type":"narrow"},{"name":"sensitive to Zymolyase","type":"narrow"},{"name":"sensitive to beta-1,3-glucan laminaripentaohydrolase","type":"narrow"},{"name":"sensitive to cell wall-degrading enzymes during mitotic cell cycle","type":"related"},{"name":"sensitive to cell wall-degrading enzymes during vegetative growth","type":"exact"},{"name":"sensitive to lysing enzymes from Trichoderma harzianum","type":"narrow"}],"termid":"FYPO:0001190"}


id: MONDO:0020791
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Meesmann corneal dystrophy","termid":"MONDO:0007379"}],"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":"corneal dystrophy, Meesmann, 1","secondary_identifiers":["UMLS:C5231499","DOID:0080670","MEDGEN:1684668","OMIM:122100"],"synonyms":[{"name":"CORNEAL DYSTROPHY, MEESMANN, 1","type":"related"},{"name":"Corneal Dystrophy, Juvenile Epithelial, of Meesmann","type":"related"},{"name":"Corneal Dystrophy, Meesmann Epithelial","type":"related"},{"name":"MECD1","type":"related"},{"name":"Meesmann Corneal Dystrophy","type":"related"},{"name":"meesmann corneal dystrophy 1","type":"exact"}],"termid":"MONDO:0020791","xrefs":{"Monarch":{"xref_id":"0020791"}}}


id: PBO:0053502
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 485","termid":"PBO:0053502"}


id: PBO:0077077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIAM Rac1 associated GEF 2","termid":"PBO:0077077"}


id: PBO:0116766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC33 antisense RNA 1","termid":"PBO:0116766"}


id: PBO:0080090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 51","termid":"PBO:0080090"}


id: MONDO:0002910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disease involving the common peroneal nerve or its branches, the deep and superficial peroneal nerves. Lesions of the deep peroneal nerve are associated with paralysis of dorsiflexion of the ankle and toes and loss of sensation from the web space between the first and second toe. Lesions of the superficial peroneal nerve result in weakness or paralysis of the peroneal muscles (which evert the foot) and loss of sensation over the dorsal and lateral surface of the leg. Traumatic injury to the common peroneal nerve near the head of the fibula is a relatively common cause of this condition. (From Joynt, Clinical Neurology, 1995, Ch51, p31)","definition_xrefs":["MESH:D020427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mononeuropathy","termid":"MONDO:0001397"}],"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":"peroneal neuropathy","secondary_identifiers":["MEDGEN:148182","DOID:4201","UMLS:C0747533","NCIT:C27596"],"synonyms":[{"name":"peroneal neuropathy","type":"exact"}],"termid":"MONDO:0002910","xrefs":{"Monarch":{"xref_id":"0002910"}}}


id: MONDO:0000570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete severe combined immunodeficiency due to artemis deficiency (obsolete MONDO:0000570)","termid":"MONDO:0000570","xrefs":{"Monarch":{"xref_id":"0000570"}}}


id: GO:0005918
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cell-cell junction that forms a continuous band around each cell in an epithelium; within the septate junction the membranes of adjacent cells maintain a constant distance of approximately 15 nm; found in arthropods.","definition_xrefs":["PMID:11700298","PMID:20795303","ISBN:0815332181","PMID:12612641","PMID:28636800"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tight junction","termid":"GO:0070160"},{"relation_name":"part_of","term_name":"apical junction complex","termid":"GO:0043296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"septate junction","secondary_identifiers":["NIF_Subcellular:sao427941916"],"synonyms":[{"name":"septate desmosome","type":"related"}],"termid":"GO:0005918"}


id: GO:0140169
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 3alpha-hydroxysteroid + NAD(P)+ = a 3-oxosteroid + NAD(P)H + H+.","definition_xrefs":["EC:1.1.1.357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0033764"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"3-alpha-hydroxysteroid 3-dehydrogenase [NAD(P)+] activity","termid":"GO:0140169"}


id: PBO:0078057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 47","termid":"PBO:0078057"}


id: PBO:0055409
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 2839","termid":"PBO:0055409"}


id: PBO:0030790
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_volume_spheroid_vegetative_cell","termid":"PBO:0030790"}


id: GO:0060051
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the glycosylation of one or more amino acid residues within a protein. Protein glycosylation is the addition of a carbohydrate or carbohydrate derivative unit to a protein amino acid, e.g. the addition of glycan chains to proteins.","definition_xrefs":["GOC:pr","GOC:dms","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glycoprotein biosynthetic process","termid":"GO:0010561"},{"relation_name":"is_a","term_name":"negative regulation of protein modification process","termid":"GO:0031400"},{"relation_name":"is_a","term_name":"regulation of protein glycosylation","termid":"GO:0060049"},{"relation_name":"negatively_regulates","term_name":"protein glycosylation","termid":"GO:0006486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006486"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006486"}],"interesting_parent_ids":["GO:0006486","GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein glycosylation","synonyms":[{"name":"negative regulation of protein amino acid glycosylation","type":"exact"}],"termid":"GO:0060051"}


id: PBO:0084835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein that may have a role in phospholipid metabolism; inner membrane protein with similarity to Mdm32p; required for normal mitochondrial morphology and inheritance; interacts genetically with MMM1, MMM2, MDM10, MDM12, and MDM34","termid":"PBO:0084835"}


id: GO:1905348
data:
  {"annotated_genes":["SJAG_03796","SJAG_02553","SJAG_03328","SJAG_02547","SJAG_02374","SJAG_04916","SJAG_01581","SJAG_03425","SJAG_03952","SJAG_03496","SJAG_04252","SJAG_00754","SJAG_01044","SJAG_04582","SJAG_03234","SJAG_01260","SJAG_02275","SJAG_01369","SJAG_00306","SJAG_06613","SJAG_01056","SJAG_01551","SJAG_00623","SJAG_00955","SJAG_04907","SJAG_03789","SJAG_01623","SJAG_04062"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[81051,76080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048476"},{"annotations":[65711,96773,120431,93511],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090730"},{"annotations":[73150,92897,117250,117162,61025,120470,73486,106379,101301,64547,72917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005655"},{"annotations":[117164,72958,81176,75336,77795,64546,73485,61024,92898,107481,107482,117252,98600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000172"},{"annotations":[120062,120436,105933,80380,73414,119048],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120330"},{"annotations":[73202,75682,80709,61127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000214"}]},"cv_name":"cellular_component","definition":"A protein complex which is capable of endonuclease activity.","definition_xrefs":["GOC:bhm","GOC:TermGenie","PMID:18413719","GO_REF:0000088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00306":null,"SJAG_00623":null,"SJAG_00754":null,"SJAG_00955":null,"SJAG_01044":null,"SJAG_01056":null,"SJAG_01260":null,"SJAG_01369":null,"SJAG_01551":null,"SJAG_01581":null,"SJAG_01623":null,"SJAG_02275":null,"SJAG_02374":null,"SJAG_02547":null,"SJAG_02553":null,"SJAG_03234":null,"SJAG_03328":null,"SJAG_03425":null,"SJAG_03496":null,"SJAG_03789":null,"SJAG_03796":null,"SJAG_03952":null,"SJAG_04062":null,"SJAG_04252":null,"SJAG_04582":null,"SJAG_04907":null,"SJAG_04916":null,"SJAG_06613":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":"endonuclease complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:1905348","terms_by_termid":{"GO:0000172":null,"GO:0000214":null,"GO:0005655":null,"GO:0048476":null,"GO:0090730":null,"GO:0120330":null}}


id: PBO:0063227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin 11 X-linked","termid":"PBO:0063227"}


id: PBO:0051260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (III)-67-2 (pseudogene)","termid":"PBO:0051260"}


id: PBO:0029730
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_1,3-beta-D-glucan_synthase_activity","termid":"PBO:0029730"}


id: MONDO:0016052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atypical autism is a pervasive developmental disorder that does not fit the diagnosis for the other specific autistic spectrum disorders (autism, Asperger syndrome, Rett syndrome or childhood disintegrative disorder) and is characterized by usually milder developmental and social delay and less stereotypical autistic behavior. '","definition_xrefs":["Orphanet:199627"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pervasive developmental disorder","termid":"MONDO:0000594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"atypical autism","secondary_identifiers":["SCTID:231536004","GARD:20336","DOID:0060042","icd11.foundation:2136163538","MEDGEN:572882","UMLS:C0338986","ICD9:299.80","MedDRA:10003747"],"termid":"MONDO:0016052","xrefs":{"Monarch":{"xref_id":"0016052"}}}


id: PBO:0068151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 458","termid":"PBO:0068151"}


id: GO:0052041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the normal execution of host programmed cell death, leading to a decrease in the frequency, rate or extent of programmed cell death in the host cell. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host programmed cell death","termid":"GO:0052040"}],"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":"symbiont-mediated suppression of host programmed cell death","synonyms":[{"name":"down regulation by symbiont of host programmed cell death","type":"exact"},{"name":"down-regulation by symbiont of host programmed cell death","type":"exact"},{"name":"downregulation by symbiont of host programmed cell death","type":"exact"},{"name":"inhibition by symbiont of host programmed cell death","type":"narrow"},{"name":"inhibition of host programmed cell death","type":"exact"},{"name":"negative regulation by symbiont of host programmed cell death","type":"exact"},{"name":"suppression by symbiont of host PCD","type":"exact"},{"name":"suppression by symbiont of host programmed cell death","type":"exact"}],"termid":"GO:0052041"}


id: GO:0002548
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a monocyte in response to an external stimulus.","definition_xrefs":["GOC:add","PMID:15173832","PMID:11696603"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte chemotaxis","termid":"GO:0030595"},{"relation_name":"is_a","term_name":"mononuclear cell migration","termid":"GO:0071674"},{"relation_name":"is_a","term_name":"myeloid leukocyte migration","termid":"GO:0097529"}],"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":"monocyte chemotaxis","termid":"GO:0002548"}


id: PBO:0031412
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-tapered_cell","termid":"PBO:0031412"}


id: PATO:0001030
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality that exists by virtue of the rate of flow of the bearer across a given surface.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement quality","termid":"PATO:0001906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"flux","termid":"PATO:0001030"}


id: MONDO:0021370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the minor salivary gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tumor of salivary gland","termid":"MONDO:0021357"},{"relation_name":"is_a","term_name":"mouth mucosa disorder","termid":"MONDO:0044992"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplasm of minor salivary gland","secondary_identifiers":["UMLS:C0345613","NCIT:C4409","SCTID:126798006","MEDGEN:138022"],"synonyms":[{"name":"minor salivary gland neoplasm","type":"exact"},{"name":"minor salivary gland neoplasm (disease)","type":"exact"},{"name":"minor salivary gland tumor","type":"exact"},{"name":"minor salivary gland tumour","type":"exact"},{"name":"neoplasm of minor salivary gland","type":"exact"},{"name":"neoplasm of the minor salivary gland","type":"exact"},{"name":"tumor of minor salivary gland","type":"exact"},{"name":"tumor of the minor salivary gland","type":"exact"},{"name":"tumour of minor salivary gland","type":"exact"},{"name":"tumour of the minor salivary gland","type":"exact"}],"termid":"MONDO:0021370","xrefs":{"Monarch":{"xref_id":"0021370"}}}


id: MONDO:0012701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract that has material basis in heterozygous mutation in the gene encoding beaded filament structural protein-2 (BFSP2) on chromosome 3q22.","definition_xrefs":["PMID:10729115","DOID:0110239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cataract","termid":"MONDO:0005129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cataract 12 multiple types","secondary_identifiers":["MESH:C566909","MEDGEN:814445","OMIM:611597","UMLS:C3808115"],"synonyms":[{"name":"CTRCT12","type":"exact"},{"name":"cataract 12, multiple types","type":"related"}],"termid":"MONDO:0012701","xrefs":{"Monarch":{"xref_id":"0012701"}}}


id: PBO:0054677
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 2084","termid":"PBO:0054677"}


id: PR:O74411
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- meu10 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74411"],"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":"meiotic expression up-regulated protein 10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1223.12c","synonyms":[{"name":"Spom972h-meu10","type":"exact"}],"termid":"PR:O74411"}


id: GO:0090452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of lithium ions (Li+) across a membrane.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lithium ion transport","termid":"GO:0010351"},{"relation_name":"is_a","term_name":"monoatomic cation transmembrane transport","termid":"GO:0098655"},{"relation_name":"is_a","term_name":"inorganic cation transmembrane transport","termid":"GO:0098662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"lithium ion transmembrane transport","synonyms":[{"name":"lithium ion import","type":"narrow"},{"name":"lithium ion uptake","type":"exact"}],"termid":"GO:0090452"}


