# terms

id: FYPO:0006156
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 sodium arsenite (AsNaO2). Cells stop growing (and may die) at a concentration of sodium arsenite that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to arsenic","termid":"FYPO:0000093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002683","FYPO:0001985","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to sodium arsenite","synonyms":[{"name":"hypersensitive to sodium arsenite","type":"exact"},{"name":"sensitive to AsNaO2","type":"exact"},{"name":"sensitive to sodium arsenite during mitotic cell cycle","type":"related"},{"name":"sensitive to sodium arsenite during vegetative growth","type":"exact"}],"termid":"FYPO:0006156"}


id: MONDO:0045043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease or disorder that involves the broad ligament of uterus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligament disorder","termid":"MONDO:0045044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disorder of uterine broad ligament","secondary_identifiers":["MEDGEN:589074","UMLS:C0404479","SCTID:237062006"],"synonyms":[{"name":"broad ligament of uterus disease","type":"exact"},{"name":"broad ligament of uterus disease or disorder","type":"exact"},{"name":"disease of broad ligament of uterus","type":"exact"},{"name":"disease or disorder of broad ligament of uterus","type":"exact"},{"name":"disorder of broad ligament","type":"exact"},{"name":"disorder of broad ligament of uterus","type":"exact"}],"termid":"MONDO:0045043","xrefs":{"Monarch":{"xref_id":"0045043"}}}


id: PBO:0075265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 18 pseudogene 18","termid":"PBO:0075265"}


id: PBO:0084156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High affinity sulfate permease; sulfate uptake is mediated by specific sulfate transporters Sul1p and Sul2p, which control the concentration of endogenous activated sulfate intermediates","termid":"PBO:0084156"}


id: PBO:0082101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AAA ATPase and SNARE disassembly chaperone; required for vesicular transport between ER and Golgi, the 'priming' step in homotypic vacuole fusion, autophagy, and protein secretion; releases Sec17p from SNAP complexes; has similarity to mammalian N-ethylmaleimide-sensitive factor (NSF)","termid":"PBO:0082101"}


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: PBO:0053289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM domain containing 2","termid":"PBO:0053289"}


id: GO:0102746
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + tetrahydrogeranylgeranyl-PP + NADPH = (E)-3,7,11,15-tetramethylhexadec-2-en-1-yl diphosphate + NADP.","definition_xrefs":["GOC:pz","EC:1.3.1.-"],"gene_count":0,"genotype_count":0,"name":"obsolete tetrahydrogeranylgeranyl-PP reductase activity (obsolete GO:0102746)","termid":"GO:0102746"}


id: PBO:0063868
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 A pseudogene 1","termid":"PBO:0063868"}


id: MONDO:0004906
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hereditary fructose intolerance syndrome (obsolete MONDO:0004906)","termid":"MONDO:0004906","xrefs":{"Monarch":{"xref_id":"0004906"}}}


id: PBO:0087450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of a complex that associates with actin filaments; forms a complex with Tda2p that inhibits barbed end F-actin assembly; elevates actin monomer pools to increase endocytotic efficiency and to regulate the distribution of actin between cables and patches; Aim21p/Tda2p forms a larger complex with actin capping proteins Cap1p and Cap2p; involved in mitochondrial migration along actin filaments; recruited to cortical actin patches by SH3 domain-containing proteins Bbc1p and Abp1p","termid":"PBO:0087450"}


id: PBO:0043217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLASP1 antisense RNA 1","termid":"PBO:0043217"}


id: PBO:0060306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYL12B pseudogene 1","termid":"PBO:0060306"}


id: PBO:0080810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-ray repair cross complementing 6","termid":"PBO:0080810"}


id: GO:0052402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The activation by an organism of the resistance gene-dependent defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by organism of symbiont resistance gene-dependent defense response (obsolete GO:0052402)","synonyms":[{"name":"activation by organism of defense response in symbiont by specific elicitors","type":"exact"},{"name":"activation by organism of pathogen-race/symbiont plant cultivar-specific resistance in symbiont","type":"exact"},{"name":"activation by organism of symbiont gene-for-gene resistance","type":"exact"},{"name":"activation by organism of symbiont resistance gene-dependent defense response","type":"exact"},{"name":"induction by organism of defense response in symbiont by specific elicitors","type":"exact"},{"name":"induction by organism of pathogen-race/symbiont plant cultivar-specific resistance in symbiont","type":"exact"},{"name":"induction by organism of symbiont gene-for-gene resistance","type":"exact"},{"name":"induction by organism of symbiont resistance gene-dependent defense response","type":"exact"}],"termid":"GO:0052402"}


id: GO:0043933
data:
  {"annotated_genes":["SJAG_00859","SJAG_03220","SJAG_00327","SJAG_03949","SJAG_00217","SJAG_02699","SJAG_04230","SJAG_05231","SJAG_01200","SJAG_03323","SJAG_01378","SJAG_03463","SJAG_00840","SJAG_04257","SJAG_04004","SJAG_01811","SJAG_00231","SJAG_01282","SJAG_01870","SJAG_02915","SJAG_02210","SJAG_04615","SJAG_02628","SJAG_02952","SJAG_02975","SJAG_04375","SJAG_01207","SJAG_02667","SJAG_01504","SJAG_01487","SJAG_01141","SJAG_03956","SJAG_04497","SJAG_01708","SJAG_05221","SJAG_02303","SJAG_01547","SJAG_00225","SJAG_02229","SJAG_04639","SJAG_02535","SJAG_00249","SJAG_00322","SJAG_02683","SJAG_00983","SJAG_00722","SJAG_04981","SJAG_01008","SJAG_01759","SJAG_02414","SJAG_03551","SJAG_03046","SJAG_02908","SJAG_03070","SJAG_00206","SJAG_00152","SJAG_02458","SJAG_02164","SJAG_02263","SJAG_03784","SJAG_00684","SJAG_02079","SJAG_02361","SJAG_03542","SJAG_00087","SJAG_02433","SJAG_00703","SJAG_01894","SJAG_01440","SJAG_04947","SJAG_02174","SJAG_02624","SJAG_02607","SJAG_02609","SJAG_03128","SJAG_04602","SJAG_00597","SJAG_06309","SJAG_04038","SJAG_00939","SJAG_00498","SJAG_04909","SJAG_00677","SJAG_03095","SJAG_04998","SJAG_01214","SJAG_03200","SJAG_02513","SJAG_00058","SJAG_03279","SJAG_03214","SJAG_05297","SJAG_02279","SJAG_02761","SJAG_00906","SJAG_05240","SJAG_04312","SJAG_03099","SJAG_04348","SJAG_01839","SJAG_03617","SJAG_02189","SJAG_02465","SJAG_04492","SJAG_03773","SJAG_00474","SJAG_02336","SJAG_03593","SJAG_01215","SJAG_00942","SJAG_02335","SJAG_04274","SJAG_04197","SJAG_00642","SJAG_04995","SJAG_03424","SJAG_04531","SJAG_00882","SJAG_04654","SJAG_02872","SJAG_03120","SJAG_02700","SJAG_01161","SJAG_02868","SJAG_03472","SJAG_02074","SJAG_02295","SJAG_04163","SJAG_07008","SJAG_01252","SJAG_02119","SJAG_04891","SJAG_01518","SJAG_03540","SJAG_00449","SJAG_00303","SJAG_02560","SJAG_00949","SJAG_01761","SJAG_02759","SJAG_02708","SJAG_03036","SJAG_00523","SJAG_02270","SJAG_00336","SJAG_02480","SJAG_01771","SJAG_04450","SJAG_02479","SJAG_03007","SJAG_03155","SJAG_01523","SJAG_02508","SJAG_04304","SJAG_01339","SJAG_04992","SJAG_02390","SJAG_03147","SJAG_00852","SJAG_01837","SJAG_01808","SJAG_01405","SJAG_03867","SJAG_04918","SJAG_01169","SJAG_03995","SJAG_01606","SJAG_00466","SJAG_02040","SJAG_03086","SJAG_04108","SJAG_00279","SJAG_01568","SJAG_04581","SJAG_05248","SJAG_01217","SJAG_00689","SJAG_01548","SJAG_03894","SJAG_04879","SJAG_02081","SJAG_02185","SJAG_05195","SJAG_02840","SJAG_03458","SJAG_03025","SJAG_04844","SJAG_00856","SJAG_03012","SJAG_04524","SJAG_03322","SJAG_01833","SJAG_02566","SJAG_02436","SJAG_01410","SJAG_04899","SJAG_04256","SJAG_01823","SJAG_02870","SJAG_02812","SJAG_02995","SJAG_01296","SJAG_02469","SJAG_01993","SJAG_04982","SJAG_01756","SJAG_02184","SJAG_01420","SJAG_05265","SJAG_04214","SJAG_04290","SJAG_04940","SJAG_03221","SJAG_03296","SJAG_01301","SJAG_02198","SJAG_00338","SJAG_03619","SJAG_00353","SJAG_02376","SJAG_02455","SJAG_00692","SJAG_04177","SJAG_05302","SJAG_03469","SJAG_00126","SJAG_02803","SJAG_03183","SJAG_04547","SJAG_00147","SJAG_03983","SJAG_04911","SJAG_03285","SJAG_00756","SJAG_04841","SJAG_00912","SJAG_02664","SJAG_02979","SJAG_06514","SJAG_00752","SJAG_04696","SJAG_03345","SJAG_06392","SJAG_04283","SJAG_07005","SJAG_02813","SJAG_01611","SJAG_00596","SJAG_03466","SJAG_02304","SJAG_00984","SJAG_05273","SJAG_04395","SJAG_03416","SJAG_03048","SJAG_00718","SJAG_04746","SJAG_05321","SJAG_04093","SJAG_00662","SJAG_00911","SJAG_03301","SJAG_00414","SJAG_03658","SJAG_04074","SJAG_04862","SJAG_04454","SJAG_03835","SJAG_01652","SJAG_03421","SJAG_02477","SJAG_03217","SJAG_00757","SJAG_00873","SJAG_02601","SJAG_04479","SJAG_04012","SJAG_05025","SJAG_05398","SJAG_02830","SJAG_03982","SJAG_00723","SJAG_01654","SJAG_00521","SJAG_04116","SJAG_01140","SJAG_01268","SJAG_01653","SJAG_04529","SJAG_00278","SJAG_01895","SJAG_03798","SJAG_01696","SJAG_00323","SJAG_00045","SJAG_01838","SJAG_01996","SJAG_01834","SJAG_02672","SJAG_02558","SJAG_00313","SJAG_03905","SJAG_00505","SJAG_02843","SJAG_00301","SJAG_04603","SJAG_04538","SJAG_03954","SJAG_04599","SJAG_01224","SJAG_07018","SJAG_04180","SJAG_03232","SJAG_04534","SJAG_00663","SJAG_04586","SJAG_04638","SJAG_00247","SJAG_01567","SJAG_01475","SJAG_03337","SJAG_03125","SJAG_04272","SJAG_02456","SJAG_06135","SJAG_02906","SJAG_04530","SJAG_03685","SJAG_00513","SJAG_05199","SJAG_05003","SJAG_02573","SJAG_05306","SJAG_04669","SJAG_00330","SJAG_06046","SJAG_06468","SJAG_01297","SJAG_02749","SJAG_01939","SJAG_00741","SJAG_04553","SJAG_03782","SJAG_01315","SJAG_00766","SJAG_02570","SJAG_04100","SJAG_04066","SJAG_03496","SJAG_00572","SJAG_05296","SJAG_01122","SJAG_00308","SJAG_03900","SJAG_02058","SJAG_03182","SJAG_01545","SJAG_00307","SJAG_04744","SJAG_02737","SJAG_03080","SJAG_05305","SJAG_02245","SJAG_05009","SJAG_00954","SJAG_03403","SJAG_05223","SJAG_01015","SJAG_04898","SJAG_03126","SJAG_02691","SJAG_00286","SJAG_06002","SJAG_05979","SJAG_01819","SJAG_02340","SJAG_02416","SJAG_03380","SJAG_01526","SJAG_02267","SJAG_00643","SJAG_04355","SJAG_00771","SJAG_02427","SJAG_02704","SJAG_02314","SJAG_01327","SJAG_04989","SJAG_01152","SJAG_04900","SJAG_03574","SJAG_01454","SJAG_01503","SJAG_04560","SJAG_02886","SJAG_04670","SJAG_02754","SJAG_01748","SJAG_05679","SJAG_00973"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73755,70314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030042"},{"annotations":[99159,65079,98046,94148],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030041"},{"annotations":[93132,99499,79609,101058,109332,111771,89948,98299,100725,113230,93538,103826,92710,112473,116106,100918,106330,107755,111137,116980,102840,119231,116105],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1902626"},{"annotations":[76664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060172"},{"annotations":[117270],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030954"},{"annotations":[72640,75831,70897],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097352"},{"annotations":[94950],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016240"},{"annotations":[76036,92648,79498,80529],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0051016"},{"annotations":[104368,73136,80033,76630,68277,98268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000492"},{"annotations":[76988,80550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000493"},{"annotations":[93118,70579,99459,116795,118024,89195,113444,115412,119147,99711,71720,80208,114550,95794,95020,107664,106690,102386,103226,90386],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034080"},{"annotations":[76863,76426,67479],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051131"},{"annotations":[118158],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000354"},{"annotations":[61643,78081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048268"},{"annotations":[80059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072318"},{"annotations":[110266,107666,113895,115735],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140529"},{"annotations":[88383,105897,117286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017004"},{"annotations":[74152,96804,109486,116357,107495,117825,109485,95132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002184"},{"annotations":[111064,87965,104369,104448,105126,104597,116903,105542,102841,92418,116904,95163,111063,97388,99783,98300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180023"},{"annotations":[65200,75444,76176,65780,72598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000730"},{"annotations":[101424],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905143"},{"annotations":[111669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070196"},{"annotations":[62080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903259"},{"annotations":[69787,75435,99251,63947,59613,72242,97175,59180,59879,64134,68773,62451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001732"},{"annotations":[78707,78285,96406,73852,118391,71760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001731"},{"annotations":[106103,58089,78252],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000349"},{"annotations":[73468,77661,105174,109871],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000350"},{"annotations":[80145,91103,105802,64608,66332,57113,66935],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0051382"},{"annotations":[104851,100414],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903359"},{"annotations":[103640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140530"},{"annotations":[78885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000707"},{"annotations":[110631,107981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010772"},{"annotations":[98943,118481,89943],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007019"},{"annotations":[71488,79361,72066],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007020"},{"annotations":[101309,106774,100409,117520,117275,100705],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051415"},{"annotations":[101310,118995],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051417"},{"annotations":[79793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046785"},{"annotations":[89546,107805,72876,104334,70610,107188,91977,62062,118681,104080,60729,117384,89351,94980,102016,59000,77067,107492,72344,94995,78878,92810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033617"},{"annotations":[101610,108705,112323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902775"},{"annotations":[70308,59096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070096"},{"annotations":[78427,73831,110049,110470,89367,74472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033615"},{"annotations":[94996,102881],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097250"},{"annotations":[71112,107809,67506,99571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034553"},{"annotations":[77177,60591,113182,78619,107914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034551"},{"annotations":[102390,95823,96259,105027,111853,98972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070126"},{"annotations":[78513,72376,57521],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902977"},{"annotations":[103981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140516"},{"annotations":[115355,110889,103642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902985"},{"annotations":[101569,73469],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000389"},{"annotations":[94324,106206,110394,110956,95927,102868,98159,95255,112699,115577,79881,110970,113608,91889,103030,95507],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000395"},{"annotations":[119050],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000348"},{"annotations":[74589,77605],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006376"},{"annotations":[75781],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010257"},{"annotations":[118278],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905560"},{"annotations":[108082],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051292"},{"annotations":[74398,80663,77308,76727,76437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006999"},{"annotations":[79164,73403,73546,96770,91437,91438,70218,108049,114871],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006334"},{"annotations":[117233,90389,97407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006337"},{"annotations":[113624,75165,113935,111599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034728"},{"annotations":[109305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006294"},{"annotations":[108586,104219],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070462"},{"annotations":[97947],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1901098"},{"annotations":[102695,117004,89973],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905561"},{"annotations":[88535,106020],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2001178"},{"annotations":[102170],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0031117"},{"annotations":[79898,90032],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045899"},{"annotations":[112296],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1904595"},{"annotations":[76811,66589,68826],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045905"},{"annotations":[58313,62616,104659,59555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043248"},{"annotations":[115179],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080129"},{"annotations":[116065,80348,99806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070682"},{"annotations":[75015,74333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0022618"},{"annotations":[76947,67293,68420,79757,77618],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0030833"},{"annotations":[76526,71678],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0003400"},{"annotations":[74410],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006449"},{"annotations":[73140,72527,72664,66306,71449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000027"},{"annotations":[118940,77419,74850,72092,75066,75559,76991,74933,70356,70186,73597,72289,72946,75075,95086,77560,73765,76914,90257,74002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000028"},{"annotations":[74252],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904802"},{"annotations":[118392,78853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990113"},{"annotations":[77856,68837,64201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001188"},{"annotations":[102516,78854,118393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990114"},{"annotations":[75276,75947,77589,94468,71694,70850,71046,77183,67581,74824,74028,72279],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051123"},{"annotations":[118394,78855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990115"},{"annotations":[72143,103389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070898"},{"annotations":[72167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010265"},{"annotations":[100442,72768,104238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000921"},{"annotations":[73331,113400],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0034462"},{"annotations":[75993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035493"},{"annotations":[76713,57482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035494"},{"annotations":[74237,76334,102061,72448,76006,105817,93703,72706,79283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000245"},{"annotations":[57266,75283,78874,104838,88095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000390"},{"annotations":[98337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000393"},{"annotations":[115449,76014,65434,77424,62518,72100,89799,73048,79650,96301,97163,104874,109310,113609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000387"},{"annotations":[72915,106877,76397,63403,78006,105818,112581,114717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000244"},{"annotations":[100959],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000388"},{"annotations":[91953,114698,115462],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006617"},{"annotations":[65155,108251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904868"},{"annotations":[108864,115271,106675,96150,116200,116735],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905323"},{"annotations":[116277,108439,100048],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905324"},{"annotations":[77847,62183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006415"},{"annotations":[106572,88910,93589,65494,93817,96877,67406,97080,71109],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007021"},{"annotations":[114182,112781,107090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903241"},{"annotations":[116877,64089,64290,102303,110489,67609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070072"}]},"cv_name":"biological_process","definition":"Any process in which macromolecules aggregate, disaggregate, or are modified, resulting in the formation, disassembly, or alteration of a protein complex.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component organization","termid":"GO:0016043"}],"gene_count":400,"genes_by_uniquename":{"SJAG_00045":null,"SJAG_00058":null,"SJAG_00087":null,"SJAG_00126":null,"SJAG_00147":null,"SJAG_00152":null,"SJAG_00206":null,"SJAG_00217":null,"SJAG_00225":null,"SJAG_00231":null,"SJAG_00247":null,"SJAG_00249":null,"SJAG_00278":null,"SJAG_00279":null,"SJAG_00286":null,"SJAG_00301":null,"SJAG_00303":null,"SJAG_00307":null,"SJAG_00308":null,"SJAG_00313":null,"SJAG_00322":null,"SJAG_00323":null,"SJAG_00327":null,"SJAG_00330":null,"SJAG_00336":null,"SJAG_00338":null,"SJAG_00353":null,"SJAG_00414":null,"SJAG_00449":null,"SJAG_00466":null,"SJAG_00474":null,"SJAG_00498":null,"SJAG_00505":null,"SJAG_00513":null,"SJAG_00521":null,"SJAG_00523":null,"SJAG_00572":null,"SJAG_00596":null,"SJAG_00597":null,"SJAG_00642":null,"SJAG_00643":null,"SJAG_00662":null,"SJAG_00663":null,"SJAG_00677":null,"SJAG_00684":null,"SJAG_00689":null,"SJAG_00692":null,"SJAG_00703":null,"SJAG_00718":null,"SJAG_00722":null,"SJAG_00723":null,"SJAG_00741":null,"SJAG_00752":null,"SJAG_00756":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00771":null,"SJAG_00840":null,"SJAG_00852":null,"SJAG_00856":null,"SJAG_00859":null,"SJAG_00873":null,"SJAG_00882":null,"SJAG_00906":null,"SJAG_00911":null,"SJAG_00912":null,"SJAG_00939":null,"SJAG_00942":null,"SJAG_00949":null,"SJAG_00954":null,"SJAG_00973":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_01008":null,"SJAG_01015":null,"SJAG_01122":null,"SJAG_01140":null,"SJAG_01141":null,"SJAG_01152":null,"SJAG_01161":null,"SJAG_01169":null,"SJAG_01200":null,"SJAG_01207":null,"SJAG_01214":null,"SJAG_01215":null,"SJAG_01217":null,"SJAG_01224":null,"SJAG_01252":null,"SJAG_01268":null,"SJAG_01282":null,"SJAG_01296":null,"SJAG_01297":null,"SJAG_01301":null,"SJAG_01315":null,"SJAG_01327":null,"SJAG_01339":null,"SJAG_01378":null,"SJAG_01405":null,"SJAG_01410":null,"SJAG_01420":null,"SJAG_01440":null,"SJAG_01454":null,"SJAG_01475":null,"SJAG_01487":null,"SJAG_01503":null,"SJAG_01504":null,"SJAG_01518":null,"SJAG_01523":null,"SJAG_01526":null,"SJAG_01545":null,"SJAG_01547":null,"SJAG_01548":null,"SJAG_01567":null,"SJAG_01568":null,"SJAG_01606":null,"SJAG_01611":null,"SJAG_01652":null,"SJAG_01653":null,"SJAG_01654":null,"SJAG_01696":null,"SJAG_01708":null,"SJAG_01748":null,"SJAG_01756":null,"SJAG_01759":null,"SJAG_01761":null,"SJAG_01771":null,"SJAG_01808":null,"SJAG_01811":null,"SJAG_01819":null,"SJAG_01823":null,"SJAG_01833":null,"SJAG_01834":null,"SJAG_01837":null,"SJAG_01838":null,"SJAG_01839":null,"SJAG_01870":null,"SJAG_01894":null,"SJAG_01895":null,"SJAG_01939":null,"SJAG_01993":null,"SJAG_01996":null,"SJAG_02040":null,"SJAG_02058":null,"SJAG_02074":null,"SJAG_02079":null,"SJAG_02081":null,"SJAG_02119":null,"SJAG_02164":null,"SJAG_02174":null,"SJAG_02184":null,"SJAG_02185":null,"SJAG_02189":null,"SJAG_02198":null,"SJAG_02210":null,"SJAG_02229":null,"SJAG_02245":null,"SJAG_02263":null,"SJAG_02267":null,"SJAG_02270":null,"SJAG_02279":null,"SJAG_02295":null,"SJAG_02303":null,"SJAG_02304":null,"SJAG_02314":null,"SJAG_02335":null,"SJAG_02336":null,"SJAG_02340":null,"SJAG_02361":null,"SJAG_02376":null,"SJAG_02390":null,"SJAG_02414":null,"SJAG_02416":null,"SJAG_02427":null,"SJAG_02433":null,"SJAG_02436":null,"SJAG_02455":null,"SJAG_02456":null,"SJAG_02458":null,"SJAG_02465":null,"SJAG_02469":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02480":null,"SJAG_02508":null,"SJAG_02513":null,"SJAG_02535":null,"SJAG_02558":null,"SJAG_02560":null,"SJAG_02566":null,"SJAG_02570":null,"SJAG_02573":null,"SJAG_02601":null,"SJAG_02607":null,"SJAG_02609":null,"SJAG_02624":null,"SJAG_02628":null,"SJAG_02664":null,"SJAG_02667":null,"SJAG_02672":null,"SJAG_02683":null,"SJAG_02691":null,"SJAG_02699":null,"SJAG_02700":null,"SJAG_02704":null,"SJAG_02708":null,"SJAG_02737":null,"SJAG_02749":null,"SJAG_02754":null,"SJAG_02759":null,"SJAG_02761":null,"SJAG_02803":null,"SJAG_02812":null,"SJAG_02813":null,"SJAG_02830":null,"SJAG_02840":null,"SJAG_02843":null,"SJAG_02868":null,"SJAG_02870":null,"SJAG_02872":null,"SJAG_02886":null,"SJAG_02906":null,"SJAG_02908":null,"SJAG_02915":null,"SJAG_02952":null,"SJAG_02975":null,"SJAG_02979":null,"SJAG_02995":null,"SJAG_03007":null,"SJAG_03012":null,"SJAG_03025":null,"SJAG_03036":null,"SJAG_03046":null,"SJAG_03048":null,"SJAG_03070":null,"SJAG_03080":null,"SJAG_03086":null,"SJAG_03095":null,"SJAG_03099":null,"SJAG_03120":null,"SJAG_03125":null,"SJAG_03126":null,"SJAG_03128":null,"SJAG_03147":null,"SJAG_03155":null,"SJAG_03182":null,"SJAG_03183":null,"SJAG_03200":null,"SJAG_03214":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03221":null,"SJAG_03232":null,"SJAG_03279":null,"SJAG_03285":null,"SJAG_03296":null,"SJAG_03301":null,"SJAG_03322":null,"SJAG_03323":null,"SJAG_03337":null,"SJAG_03345":null,"SJAG_03380":null,"SJAG_03403":null,"SJAG_03416":null,"SJAG_03421":null,"SJAG_03424":null,"SJAG_03458":null,"SJAG_03463":null,"SJAG_03466":null,"SJAG_03469":null,"SJAG_03472":null,"SJAG_03496":null,"SJAG_03540":null,"SJAG_03542":null,"SJAG_03551":null,"SJAG_03574":null,"SJAG_03593":null,"SJAG_03617":null,"SJAG_03619":null,"SJAG_03658":null,"SJAG_03685":null,"SJAG_03773":null,"SJAG_03782":null,"SJAG_03784":null,"SJAG_03798":null,"SJAG_03835":null,"SJAG_03867":null,"SJAG_03894":null,"SJAG_03900":null,"SJAG_03905":null,"SJAG_03949":null,"SJAG_03954":null,"SJAG_03956":null,"SJAG_03982":null,"SJAG_03983":null,"SJAG_03995":null,"SJAG_04004":null,"SJAG_04012":null,"SJAG_04038":null,"SJAG_04066":null,"SJAG_04074":null,"SJAG_04093":null,"SJAG_04100":null,"SJAG_04108":null,"SJAG_04116":null,"SJAG_04163":null,"SJAG_04177":null,"SJAG_04180":null,"SJAG_04197":null,"SJAG_04214":null,"SJAG_04230":null,"SJAG_04256":null,"SJAG_04257":null,"SJAG_04272":null,"SJAG_04274":null,"SJAG_04283":null,"SJAG_04290":null,"SJAG_04304":null,"SJAG_04312":null,"SJAG_04348":null,"SJAG_04355":null,"SJAG_04375":null,"SJAG_04395":null,"SJAG_04450":null,"SJAG_04454":null,"SJAG_04479":null,"SJAG_04492":null,"SJAG_04497":null,"SJAG_04524":null,"SJAG_04529":null,"SJAG_04530":null,"SJAG_04531":null,"SJAG_04534":null,"SJAG_04538":null,"SJAG_04547":null,"SJAG_04553":null,"SJAG_04560":null,"SJAG_04581":null,"SJAG_04586":null,"SJAG_04599":null,"SJAG_04602":null,"SJAG_04603":null,"SJAG_04615":null,"SJAG_04638":null,"SJAG_04639":null,"SJAG_04654":null,"SJAG_04669":null,"SJAG_04670":null,"SJAG_04696":null,"SJAG_04744":null,"SJAG_04746":null,"SJAG_04841":null,"SJAG_04844":null,"SJAG_04862":null,"SJAG_04879":null,"SJAG_04891":null,"SJAG_04898":null,"SJAG_04899":null,"SJAG_04900":null,"SJAG_04909":null,"SJAG_04911":null,"SJAG_04918":null,"SJAG_04940":null,"SJAG_04947":null,"SJAG_04981":null,"SJAG_04982":null,"SJAG_04989":null,"SJAG_04992":null,"SJAG_04995":null,"SJAG_04998":null,"SJAG_05003":null,"SJAG_05009":null,"SJAG_05025":null,"SJAG_05195":null,"SJAG_05199":null,"SJAG_05221":null,"SJAG_05223":null,"SJAG_05231":null,"SJAG_05240":null,"SJAG_05248":null,"SJAG_05265":null,"SJAG_05273":null,"SJAG_05296":null,"SJAG_05297":null,"SJAG_05302":null,"SJAG_05305":null,"SJAG_05306":null,"SJAG_05321":null,"SJAG_05398":null,"SJAG_05679":null,"SJAG_05979":null,"SJAG_06002":null,"SJAG_06046":null,"SJAG_06135":null,"SJAG_06309":null,"SJAG_06392":null,"SJAG_06468":null,"SJAG_06514":null,"SJAG_07005":null,"SJAG_07008":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein-containing complex organization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:0034600","GO:0034621","GO:0071822"],"synonyms":[{"name":"cellular macromolecular complex organization","type":"related"},{"name":"cellular macromolecular complex subunit organisation","type":"related"},{"name":"cellular macromolecular complex subunit organization","type":"related"},{"name":"macromolecular complex organization","type":"related"},{"name":"macromolecular complex subunit organisation","type":"related"},{"name":"macromolecular complex subunit organization","type":"related"},{"name":"protein complex subunit organisation","type":"exact"},{"name":"protein complex subunit organization","type":"exact"},{"name":"protein-containing complex subunit organization","type":"related"}],"termid":"GO:0043933","terms_by_termid":{"GO:0000027":null,"GO:0000028":null,"GO:0000244":null,"GO:0000245":null,"GO:0000348":null,"GO:0000349":null,"GO:0000350":null,"GO:0000354":null,"GO:0000387":null,"GO:0000388":null,"GO:0000389":null,"GO:0000390":null,"GO:0000393":null,"GO:0000395":null,"GO:0000492":null,"GO:0000493":null,"GO:0000707":null,"GO:0000730":null,"GO:0000921":null,"GO:0001188":null,"GO:0001731":null,"GO:0001732":null,"GO:0002184":null,"GO:0003400":null,"GO:0006294":null,"GO:0006334":null,"GO:0006337":null,"GO:0006376":null,"GO:0006415":null,"GO:0006449":null,"GO:0006617":null,"GO:0006999":null,"GO:0007019":null,"GO:0007020":null,"GO:0007021":null,"GO:0010257":null,"GO:0010265":null,"GO:0010772":null,"GO:0016240":null,"GO:0017004":null,"GO:0022618":null,"GO:0030041":null,"GO:0030042":null,"GO:0030833":null,"GO:0030954":null,"GO:0031117":null,"GO:0033615":null,"GO:0033617":null,"GO:0034080":null,"GO:0034462":null,"GO:0034551":null,"GO:0034553":null,"GO:0034728":null,"GO:0035493":null,"GO:0035494":null,"GO:0043248":null,"GO:0045899":null,"GO:0045905":null,"GO:0046785":null,"GO:0048268":null,"GO:0051016":null,"GO:0051123":null,"GO:0051131":null,"GO:0051292":null,"GO:0051382":null,"GO:0051415":null,"GO:0051417":null,"GO:0060172":null,"GO:0070072":null,"GO:0070096":null,"GO:0070126":null,"GO:0070196":null,"GO:0070462":null,"GO:0070682":null,"GO:0070898":null,"GO:0072318":null,"GO:0080129":null,"GO:0097250":null,"GO:0097352":null,"GO:0140516":null,"GO:0140529":null,"GO:0140530":null,"GO:0180023":null,"GO:1901098":null,"GO:1902626":null,"GO:1902775":null,"GO:1902977":null,"GO:1902985":null,"GO:1903241":null,"GO:1903259":null,"GO:1903359":null,"GO:1904595":null,"GO:1904802":null,"GO:1904868":null,"GO:1905143":null,"GO:1905323":null,"GO:1905324":null,"GO:1905560":null,"GO:1905561":null,"GO:1990113":null,"GO:1990114":null,"GO:1990115":null,"GO:2001178":null}}


id: FYPO:0001045
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of acid phosphatase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal acid phosphatase activity","termid":"FYPO:0001044"},{"relation_name":"is_a","term_name":"decreased phosphatase activity","termid":"FYPO:0004304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0001985","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"decreased acid phosphatase activity","synonyms":[{"name":"reduced acid phosphatase activity","type":"exact"}],"termid":"FYPO:0001045"}


id: PBO:0067983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 285","termid":"PBO:0067983"}


id: PBO:0059753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 27","termid":"PBO:0059753"}


id: PATO:0000718
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A viability quality inhering in a population by virtue of the bearer's long term survival inability.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viability","termid":"PATO:0000169"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lethal (sensu genetics)","termid":"PATO:0000718"}


id: GO:0003941
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-serine = pyruvate + NH3.","definition_xrefs":["EC:4.3.1.17"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ammonia-lyase activity","termid":"GO:0016841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"L-serine ammonia-lyase activity","secondary_identifiers":["MetaCyc:4.3.1.17-RXN","RHEA:19169"],"synonyms":[{"name":"L-hydroxyaminoacid dehydratase activity","type":"broad"},{"name":"L-serine ammonia-lyase (pyruvate-forming) activity","type":"related"},{"name":"L-serine deaminase activity","type":"exact"},{"name":"L-serine dehydratase activity","type":"broad"},{"name":"L-serine dehydration activity","type":"related"},{"name":"L-serine hydro-lyase (deaminating) activity","type":"exact"},{"name":"serine deaminase activity","type":"broad"}],"termid":"GO:0003941"}


id: GO:0022028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of cells in the telencephalon from the subventricular zone to the olfactory bulb in which cells move orthogonally to the direction of radial migration and do not use radial glial cell processes as substrates for migration.","definition_xrefs":["GOC:dgh","GOC:jid","GO_REF:0000021","GOC:dph","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telencephalon cell migration","termid":"GO:0022029"},{"relation_name":"part_of","term_name":"olfactory bulb development","termid":"GO:0021772"}],"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":"tangential migration from the subventricular zone to the olfactory bulb","synonyms":[{"name":"rostral migratory stream migration","type":"exact"}],"termid":"GO:0022028"}


id: MONDO:0800031
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":"central hypoventilation syndrome, congenital","secondary_identifiers":["OMIMPS:209880","UMLS:C1275808","MEDGEN:220902"],"termid":"MONDO:0800031","xrefs":{"Monarch":{"xref_id":"0800031"}}}


id: GO:0045046
data:
  {"annotated_genes":["SJAG_03781","SJAG_04763","SJAG_03440"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90752,95751,111721],"is_not":false,"summary":null,"term":"GO:0045046"}]},"cv_name":"biological_process","definition":"The targeting of proteins into the peroxisomal membrane. The process is not well understood, but both signals and mechanism differ from those involved in peroxisomal matrix protein import.","definition_xrefs":["PMID:11687502","ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein transport","termid":"GO:0006886"},{"relation_name":"is_a","term_name":"peroxisomal membrane transport","termid":"GO:0015919"},{"relation_name":"is_a","term_name":"establishment of protein localization to peroxisome","termid":"GO:0072663"},{"relation_name":"is_a","term_name":"establishment of protein localization to membrane","termid":"GO:0090150"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03440":null,"SJAG_03781":null,"SJAG_04763":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0007031"}],"interesting_parent_ids":["GO:0051179","GO:0007031","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"protein import into peroxisome membrane","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9603798"],"synonyms":[{"name":"peroxisome membrane protein import","type":"exact"},{"name":"protein transport into peroxisome membrane","type":"exact"}],"termid":"GO:0045046","terms_by_termid":{"GO:0045046":null}}


id: GO:0085018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a host organism maintains the structure and function of a symbiont-containing vacuole. The symbiont-containing vacuole is a membrane-bounded vacuole within a host cell in which a symbiont organism resides, and can serve to reduce pathogenicity of invading symbionts by restricting them to the vacuolar compartment.","definition_xrefs":["GOC:jl","GOC:yaf","PMID:18665841"],"gene_count":0,"genotype_count":0,"name":"obsolete maintenance of symbiont-containing vacuole by host (obsolete GO:0085018)","synonyms":[{"name":"maintenance of parasitophorous vacuole","type":"exact"},{"name":"maintenance of pathogen-containing vacuole","type":"exact"},{"name":"maintenance of vacuolar integrity during bacterial infection","type":"narrow"}],"termid":"GO:0085018"}


id: PBO:0090814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation initiation factor Mti3","termid":"PBO:0090814"}


id: PBO:0088113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar aspartate and glutamate exporter; member of a family of seven genes (AVT1-7) related to vesicular GABA-glycine transporters; involved in compartmentalizing acidic amino acids in response to nitrogen starvation; AVT6 has a paralog, AVT5, that arose from the whole genome duplication","termid":"PBO:0088113"}


id: PBO:0058487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5681b","termid":"PBO:0058487"}


id: MONDO:1012016
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive ataxia with degenerative thoracic myelopathy, non-human animal","termid":"MONDO:1011829"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive ataxia with degenerative thoracic myelopathy, sheep","secondary_identifiers":["OMIA:000079-9940"],"termid":"MONDO:1012016","xrefs":{"Monarch":{"xref_id":"1012016"}}}


id: FYPO:0004265
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the cortical microtubule cytoskeleton is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton","termid":"FYPO:0004090"},{"relation_name":"is_a","term_name":"abnormal protein localization to cell cortex","termid":"FYPO:0006867"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization to cortical microtubule cytoskeleton","synonyms":[{"name":"abnormal protein localisation to cortical microtubule cytoskeleton","type":"exact"}],"termid":"FYPO:0004265"}


id: PBO:0071515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 18","termid":"PBO:0071515"}


id: PATO:0001756
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A conductivity quality inhering in a bearer by virtue of the bearer's disposition to spontaneous transfer of thermal energy from a region of higher temperature to a region of lower temperature.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Heat_conduction"],"direct_ancestors":[{"relation_name":"is_a","term_name":"conductivity","termid":"PATO:0001585"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat conductivity","synonyms":[{"name":"thermal conduction","type":"exact"}],"termid":"PATO:0001756"}


id: GO:0031138
data:
  {"annotated_genes":["SJAG_01311","SJAG_01699","SJAG_01754","SJAG_03048","SJAG_02773","SJAG_02592","SJAG_01919","SJAG_04682","SJAG_00600","SJAG_00472","SJAG_00526","SJAG_04312","SJAG_02730","SJAG_00975","SJAG_02426","SJAG_01401","SJAG_02266","SJAG_01084","SJAG_04026","SJAG_00145","SJAG_01254","SJAG_03081","SJAG_02723","SJAG_02921","SJAG_04394","SJAG_02444"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89133,92411,93543,96713,101941,102683,105237,116892],"is_not":false,"summary":null,"term":"GO:0031138"},{"annotations":[95482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140538"},{"annotations":[109337,91732,94552,100865,102168,107172,106235,94692,114799,104819,88525,115862,93252,106138,116399,106822,106976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010515"}]},"cv_name":"biological_process","definition":"Any process that decreases the rate or frequency of conjugation with cellular fusion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of conjugation with cellular fusion","termid":"GO:0031137"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"negatively_regulates","term_name":"conjugation with cellular fusion","termid":"GO:0000747"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00145":null,"SJAG_00472":null,"SJAG_00526":null,"SJAG_00600":null,"SJAG_00975":null,"SJAG_01084":null,"SJAG_01254":null,"SJAG_01311":null,"SJAG_01401":null,"SJAG_01699":null,"SJAG_01754":null,"SJAG_01919":null,"SJAG_02266":null,"SJAG_02426":null,"SJAG_02444":null,"SJAG_02592":null,"SJAG_02723":null,"SJAG_02730":null,"SJAG_02773":null,"SJAG_02921":null,"SJAG_03048":null,"SJAG_03081":null,"SJAG_04026":null,"SJAG_04312":null,"SJAG_04394":null,"SJAG_04682":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0000747"}],"interesting_parent_ids":["GO:0008150","GO:0000747"],"is_obsolete":false,"name":"negative regulation of conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of conjugation with cellular fusion","type":"exact"},{"name":"down-regulation of conjugation with cellular fusion","type":"exact"},{"name":"downregulation of conjugation with cellular fusion","type":"exact"},{"name":"inhibition of conjugation with cellular fusion","type":"narrow"}],"termid":"GO:0031138","terms_by_termid":{"GO:0010515":null,"GO:0031138":null,"GO:0140538":null}}


id: FYPO:0003872
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of glutathione measured in a cell is higher than normal when the cell is in G0 phase.","definition_xrefs":["PMID:20133687","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during G0","termid":"FYPO:0002949"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased glutathione level during G0","synonyms":[{"name":"increased glutathione accumulation during G0","type":"related"},{"name":"increased glutathione level during cell quiescence","type":"exact"},{"name":"increased glutathione level during quiescence","type":"exact"}],"termid":"FYPO:0003872"}


id: GO:0035915
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components by an organism to form a pore complex in a membrane of another organism.","definition_xrefs":["GOC:fj","GOC:bf","PMID:21549739"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disruption of plasma membrane integrity in another organism","termid":"GO:0051673"}],"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":"pore formation in membrane of another organism","synonyms":[{"name":"pore complex assembly in other organism","type":"exact"},{"name":"pore complex biogenesis in other organism","type":"exact"},{"name":"pore formation in membrane of other organism","type":"exact"},{"name":"pore formation in other organism","type":"exact"},{"name":"pore-forming toxin activity","type":"related"}],"termid":"GO:0035915"}


id: GO:1905956
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of endothelial tube morphogenesis.","definition_xrefs":["PMID:25961718","GO_REF:0000058","GOC:BHF_miRNA","GOC:rph","GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of endothelial tube morphogenesis","termid":"GO:1901509"},{"relation_name":"is_a","term_name":"positive regulation of morphogenesis of an epithelium","termid":"GO:1905332"},{"relation_name":"positively_regulates","term_name":"endothelial tube morphogenesis","termid":"GO:0061154"}],"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 endothelial tube morphogenesis","synonyms":[{"name":"activation of endothelial tube morphogenesis","type":"narrow"},{"name":"up regulation of endothelial tube morphogenesis","type":"exact"},{"name":"up-regulation of endothelial tube morphogenesis","type":"exact"},{"name":"upregulation of endothelial tube morphogenesis","type":"exact"}],"termid":"GO:1905956"}


id: PBO:0063669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piggyBac transposable element derived 1","termid":"PBO:0063669"}


id: PBO:0066724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 21","termid":"PBO:0066724"}


id: GO:0018541
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,4-benzoquinone + H+ + NADPH = hydroquinone + NADP+.","definition_xrefs":["RHEA:23488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor","termid":"GO:0016655"}],"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":"p-benzoquinone reductase (NADPH) activity","secondary_identifiers":["EC:1.6.5.6","KEGG_REACTION:R05244","MetaCyc:1.6.5.6-RXN"],"synonyms":[{"name":"NADPH:p-benzoquinone oxidoreductase activity","type":"related"}],"termid":"GO:0018541"}


id: PBO:0040952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein 3 pseudogene 23","termid":"PBO:0040952"}


id: GO:0050138
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + NADP+ + nicotinate = 6-hydroxynicotinate + H+ + NADPH.","definition_xrefs":["RHEA:12236","EC:1.17.1.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH or CH2 groups, NAD or NADP as acceptor","termid":"GO:0016726"}],"gene_count":0,"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:0003674","GO:0016491"],"is_obsolete":false,"name":"nicotinate dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R01720","MetaCyc:RXN-7637"],"synonyms":[{"name":"nicotinate hydroxylase activity","type":"related"},{"name":"nicotinate:NADP+ 6-oxidoreductase (hydroxylating)","type":"related"},{"name":"nicotinic acid hydroxylase activity","type":"related"}],"termid":"GO:0050138"}


id: PBO:0001884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein WIPI family","termid":"PBO:0001884"}


id: PBO:0056714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MEMO1 pseudogene 6","termid":"PBO:0056714"}


id: PBO:0072809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterile alpha motif domain containing 4B","termid":"PBO:0072809"}


id: PBO:0042297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD6 molecule","termid":"PBO:0042297"}


id: GO:0009788
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of abscisic acid (ABA) signaling.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of abscisic acid-activated signaling pathway","termid":"GO:0009787"},{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"negative regulation of cellular response to alcohol","termid":"GO:1905958"},{"relation_name":"negatively_regulates","term_name":"abscisic acid-activated signaling pathway","termid":"GO:0009738"}],"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:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of abscisic acid-activated signaling pathway","synonyms":[{"name":"down regulation of abscisic acid mediated signaling","type":"exact"},{"name":"down-regulation of abscisic acid mediated signaling","type":"exact"},{"name":"downregulation of abscisic acid mediated signaling","type":"exact"},{"name":"inhibition of abscisic acid mediated signaling","type":"narrow"},{"name":"negative regulation of abscisic acid mediated signaling pathway","type":"related"},{"name":"negative regulation of abscisic acid mediated signalling","type":"exact"}],"termid":"GO:0009788"}


id: PBO:0061028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIM1 serine/threonine protein kinase","termid":"PBO:0061028"}


id: PBO:0056873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MHC class I polypeptide-related sequence C (pseudogene)","termid":"PBO:0056873"}


id: PBO:0060182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucin 3A, cell surface associated","termid":"PBO:0060182"}


id: PBO:0034175
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-immediately_causally_downstream_of","termid":"PBO:0034175"}


id: PBO:0112993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adenosine 5'-monophosphoramidase; interacts physically and genetically with CDK and TFIIK subunit Kin28p, and genetically with CAK1; member of histidine triad (HIT) superfamily of nucleotide-binding proteins; protein abundance increases in response to DNA replication stress; human homolog HINT1 can complement yeast hnt1 mutant","termid":"PBO:0112993"}


id: PBO:0085738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in transcription initiation; acts at TATA-containing promoters; associates with the basal transcription factor TFIID; contains two bromodomains; corresponds to the C-terminal region of mammalian TAF1; redundant with Bdf1p; protein abundance increases in response to DNA replication stress; BDF2 has a paralog, BDF1, that arose from the whole genome duplication","termid":"PBO:0085738"}


id: MONDO:0002480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant epithelial tumor of the female reproductive system characterized by the presence of glands and/or cysts lined by neoplastic cells that resemble endometrial cells.","definition_xrefs":["NCIT:C7113"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"female reproductive organ cancer","termid":"MONDO:0001416"},{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"},{"relation_name":"is_a","term_name":"female reproductive system neoplasm","termid":"MONDO:0021148"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endometrioid tumor","secondary_identifiers":["DOID:3001","MEDGEN:105374","UMLS:C0474809"],"synonyms":[{"name":"endometrioid neoplasm","type":"exact"},{"name":"endometrioid neoplasm of female reproductive system","type":"exact"},{"name":"endometrioid neoplasm of the female reproductive system","type":"exact"},{"name":"endometrioid tumor","type":"exact"},{"name":"endometrioid tumor (morphologic abnormality)","type":"exact"},{"name":"endometrioid tumor of female reproductive system","type":"exact"},{"name":"endometrioid tumor of the female reproductive system","type":"exact"},{"name":"endometrioid tumour (morphologic abnormality)","type":"exact"},{"name":"endometrioid tumour of female reproductive system","type":"exact"},{"name":"endometrioid tumour of the female reproductive system","type":"exact"},{"name":"female reproductive endometrioid cancer","type":"related"},{"name":"female reproductive endometrioid neoplasm","type":"exact"},{"name":"female reproductive endometrioid tumor","type":"exact"},{"name":"female reproductive endometrioid tumour","type":"exact"}],"termid":"MONDO:0002480","xrefs":{"Monarch":{"xref_id":"0002480"}}}


id: FYPO:0005960
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which a mitotic spindle forms with microtubules emanating from three or more poles.","definition_xrefs":["PomBase:mah","PMID:15797925"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic spindle","termid":"FYPO:0000338"},{"relation_name":"is_a","term_name":"multipolar spindle","termid":"FYPO:0005959"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000054","FYPO:0002399","FYPO:0000120","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"multipolar mitotic spindle","synonyms":[{"name":"multipolar spindle during mitosis","type":"exact"},{"name":"multipolar spindle during vegetative growth","type":"exact"}],"termid":"FYPO:0005960"}


id: PBO:0055289
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 2716","termid":"PBO:0055289"}


id: PBO:0052939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 23-1","termid":"PBO:0052939"}


id: PR:O74783
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An F-box/LRR-repeat protein 14 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03350"],"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":"SCF E3 ubiquitin ligase complex F-box protein pof2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC25B2.11","secondary_identifiers":["UniProtKB:O74783"],"synonyms":[{"name":"F-box and leucine-rich repeat protein pof2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"F-box protein pof2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"F-box/LRR-repeat protein pof2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-FBXL14","type":"exact"}],"termid":"PR:O74783"}


id: MONDO:1012530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cavitating leukodystrophy, non-human animal","termid":"MONDO:1011897"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cavitating leukodystrophy, dog","secondary_identifiers":["OMIA:002214-9615"],"termid":"MONDO:1012530","xrefs":{"Monarch":{"xref_id":"1012530"}}}


id: GO:0018698
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: AH2 + chloroethene = A + chloride + ethene + H+.","definition_xrefs":["RHEA:68004","PMID:9171062","PMID:15294827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on X-H and Y-H to form an X-Y bond","termid":"GO:0046992"}],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"chloroethene reductive dehalogenase activity","secondary_identifiers":["UM-BBD_reactionID:r0352","MetaCyc:VCREDCHLOR-RXN"],"synonyms":[{"name":"vinyl chloride reductive dehalogenase activity","type":"exact"}],"termid":"GO:0018698"}


id: MONDO:0000613
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete estrogen-receptor positive breast cancer (obsolete MONDO:0000613)","termid":"MONDO:0000613","xrefs":{"Monarch":{"xref_id":"0000613"}}}


id: PBO:0091072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hrd1 ubiquitin ligase complex E3 subunit Hrd1","termid":"PBO:0091072"}


id: FYPO:0004458
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of one or more DNA replication RNAs measured in a cell is higher than normal (i.e. higher than observed in wild-type cells) when the cell is subject to nitrogen starvation. DNA replication RNAs are transcribed from genes whose products are involved in DNA replication.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during nitrogen starvation","termid":"FYPO:0002020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased level of DNA replication gene mRNA during nitrogen starvation","synonyms":[{"name":"increased DNA replication gene mRNA accumulation during nitrogen starvation","type":"related"},{"name":"increased level of DNA replication gene RNA during nitrogen starvation","type":"exact"},{"name":"increased level of DNA replication gene mRNA during nitrogen depletion","type":"exact"},{"name":"increased level of DNA replication gene mRNA during nitrogen deprivation","type":"exact"},{"name":"increased level of DNA replication gene transcripts nitrogen starvation","type":"exact"}],"termid":"FYPO:0004458"}


id: MOD:00703
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with a group derived from an isoprene polymer, such as a geranyl (C10), farnesyl (C15) or geranylgeranyl (C20) group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkylated residue","termid":"MOD:00001"},{"relation_name":"is_a","term_name":"lipoconjugated residue","termid":"MOD:01155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"isoprenylated residue","synonyms":[{"name":"IpRes","type":"exact"}],"termid":"MOD:00703"}


id: PBO:0034637
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_UV-damage_excision_repair_during_mitotic_G2_phase","termid":"PBO:0034637"}


id: GO:1905803
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellular response to manganese ion.","definition_xrefs":["GO_REF:0000058","PMID:23721876","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of cellular response to manganese ion","termid":"GO:1905802"},{"relation_name":"negatively_regulates","term_name":"cellular response to manganese ion","termid":"GO:0071287"}],"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 cellular response to manganese ion","synonyms":[{"name":"down regulation of cellular response to manganese","type":"exact"},{"name":"down regulation of cellular response to manganese ion","type":"exact"},{"name":"down-regulation of cellular response to manganese","type":"exact"},{"name":"down-regulation of cellular response to manganese ion","type":"exact"},{"name":"downregulation of cellular response to manganese","type":"exact"},{"name":"downregulation of cellular response to manganese ion","type":"exact"},{"name":"inhibition of cellular response to manganese","type":"narrow"},{"name":"inhibition of cellular response to manganese ion","type":"narrow"},{"name":"negative regulation of cellular response to manganese","type":"exact"}],"termid":"GO:1905803"}


id: PBO:0067280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 361, pseudogene","termid":"PBO:0067280"}


id: PBO:0065287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich transmembrane protein 2","termid":"PBO:0065287"}


id: MONDO:0017868
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, non-syndromic cerebral malformation characterized by severe intellectual disability, progressive postnatal microcephaly, axial hypotonia, spastic quadriparesis, seizures and facial dysmorphism (bushy eyebrows, hairy forehead, broad nasal root, long flat philtrum, V-shaped upper lip). Additionally, talipes equinovarus, non-obstructive cardiomyopathy, persistent hyperplastic primary vitreous, obstructive hydrocephalus and autistic features may also be associated. On brain magnetic resonance imaging, the 'butterfly sign' is characterisitcally observed and cortical calcifications, agenesis of the corpus callosum, ventriculomegaly, brainstem dysplasia and cerebellar vermis hypoplasia have also been described.","definition_xrefs":["Orphanet:319192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diencephalic-mesencephalic junction dysplasia","secondary_identifiers":["MEDGEN:1641855","UMLS:C4707858","OMIMPS:251280","GARD:21407"],"synonyms":[{"name":"diencephalic-mesencephalic junction dysplasia syndrome","type":"exact"}],"termid":"MONDO:0017868","xrefs":{"Monarch":{"xref_id":"0017868"}}}


id: MONDO:0800156
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder of amino acid metabolism that has its basis in the disruption of the metabolism of ornithine, proline and/or hydroxyproline.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of amino acid metabolism","termid":"MONDO:0004736"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"inborn disorder of ornithine, proline and hydroxyproline metabolism","termid":"MONDO:0800156","xrefs":{"Monarch":{"xref_id":"0800156"}}}


id: PBO:0051097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy constant mu","termid":"PBO:0051097"}


id: PBO:0058081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4299","termid":"PBO:0058081"}


id: PBO:0084064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase-activating protein (RhoGAP) for Cdc42p and Rho5p; relocalizes from bud neck to cytoplasm upon DNA replication stress","termid":"PBO:0084064"}


id: MONDO:0003639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that arises from the hilar region of the lung.","definition_xrefs":["NCIT:C5671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung neoplasm","termid":"MONDO:0021117"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lung hilum neoplasm","secondary_identifiers":["DOID:5767","MEDGEN:224849","SCTID:126707007","UMLS:C1290358"],"synonyms":[{"name":"hilar lung neoplasm","type":"exact"},{"name":"hilar lung tumor","type":"exact"},{"name":"hilar lung tumour","type":"exact"},{"name":"lung hilum neoplasm","type":"exact"},{"name":"lung hilum tumor","type":"exact"},{"name":"lung hilum tumour","type":"exact"},{"name":"lung hilus neoplasm","type":"exact"},{"name":"lung hilus neoplasm (disease)","type":"exact"},{"name":"lung hilus tumor","type":"exact"},{"name":"lung hilus tumour","type":"exact"},{"name":"neoplasm of hilus of lung","type":"exact"},{"name":"neoplasm of lung hilus","type":"exact"},{"name":"tumor of lung hilus","type":"exact"},{"name":"tumour of lung hilus","type":"exact"}],"termid":"MONDO:0003639","xrefs":{"Monarch":{"xref_id":"0003639"}}}


id: PBO:0113130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Evolutionarily-conserved 5'-3' exonuclease; deNADding enzyme that modulates mitochondrial NAD-capped RNA; component of cytoplasmic P-bodies involved in mRNA decay; positively regulates transcription initiation and elongation; involved in microtubule-mediated processes, filamentous growth, ribosomal RNA maturation, telomere maintenance, and tRNA intron turnover; negative regulator of autophagy; activated by scavenger decapping enzyme Dcs1p; role in preventing L-A mycovirus pathogenesis","termid":"PBO:0113130"}


id: GO:0015842
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The active transport of aminergic neurotransmitters into a synaptic vesicle. This import is fuelled by an electrochemical gradient across the vesicle membrane, established by the action proton pumps.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amine transport","termid":"GO:0015837"},{"relation_name":"is_a","term_name":"neurotransmitter loading into synaptic vesicle","termid":"GO:0098700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"aminergic neurotransmitter loading into synaptic vesicle","termid":"GO:0015842"}


id: PBO:0091712
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"facilitates Rad51 assembly at damage sites independently of Rad57","termid":"PBO:0091712"}


id: MONDO:0017733
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-mannosidosis","termid":"MONDO:0009561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0005328","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"alpha-mannosidosis, adult form","secondary_identifiers":["MEDGEN:1843432","NANDO:2201189","UMLS:C5679974","NANDO:1200128","GTR:AN0103810","SCTID:58112007","Orphanet:309288","GARD:17408","GTR:AN0103811"],"synonyms":[{"name":"Alpha-mannosidosis adult-onset form","type":"related"},{"name":"lysosomal alpha-D-mannosidase deficiency, adult form","type":"exact"}],"termid":"MONDO:0017733","xrefs":{"Monarch":{"xref_id":"0017733"}}}


id: GO:0071924
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of chemokine (C-C motif) ligand 22 (CCL22) due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["PMID:18832724","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine production","termid":"GO:0032602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"chemokine (C-C motif) ligand 22 production","synonyms":[{"name":"C-C motif chemokine 22 production","type":"exact"},{"name":"CCL-22 production","type":"exact"},{"name":"CCL22 production","type":"exact"}],"termid":"GO:0071924"}


id: PBO:0084188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Histone H1, linker histone with roles in meiosis and sporulation; decreasing levels early in sporulation may promote meiosis, and increasing levels during sporulation facilitate compaction of spore chromatin; binds to promoters and within genes in mature spores; may be recruited by Ume6p to promoter regions, contributing to transcriptional repression outside of meiosis; suppresses DNA repair involving homologous recombination","termid":"PBO:0084188"}


id: PBO:0062984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTGS2 antisense NFKB1 complex-mediated expression regulator RNA","termid":"PBO:0062984"}


id: MONDO:0014112
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85352],"is_not":false,"summary":null,"term":"MONDO:0014112"}]},"cv_name":"mondo","definition":"Any cardiofaciocutaneous syndrome in which the cause of the disease is a mutation in the KRAS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiofaciocutaneous syndrome","termid":"MONDO:0015280"}],"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:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005267"],"is_obsolete":false,"name":"cardiofaciocutaneous syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:815335","GARD:15935","OMIM:615278","DOID:0111461","UMLS:C3809005"],"synonyms":[{"name":"CFC2","type":"related"},{"name":"KRAS cardiofaciocutaneous syndrome","type":"exact"},{"name":"cardiofaciocutaneous syndrome 2","type":"exact"},{"name":"cardiofaciocutaneous syndrome caused by mutation in KRAS","type":"exact"},{"name":"cardiofaciocutaneous syndrome caused by mutation in kras","type":"exact"},{"name":"cardiofaciocutaneous syndrome type 2","type":"exact"},{"name":"kras cardiofaciocutaneous syndrome","type":"exact"}],"termid":"MONDO:0014112","terms_by_termid":{"MONDO:0014112":null},"xrefs":{"Monarch":{"xref_id":"0014112"}}}


id: PBO:0089196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar DNAJ domain protein, DNAJC9 family, implicated in mRNA splicing","termid":"PBO:0089196"}


id: MONDO:0010717
data:
  {"annotated_genes":["SJAG_02006"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86765],"is_not":false,"summary":null,"term":"MONDO:0010717"}]},"cv_name":"mondo","definition":"Pyruvate dehydrogenase E1-alpha deficiency is the most frequent form of pyruvate dehydrogenase deficiency (PDHD) characterized by variable lactic acidosis, impaired psychomotor development, hypotonia and neurological dysfunction.","definition_xrefs":["Orphanet:79243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate dehydrogenase deficiency","termid":"MONDO:0019169"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02006":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066","MONDO:0005244","MONDO:0037792"],"is_obsolete":false,"name":"pyruvate dehydrogenase E1-alpha deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:326486","SCTID:124593001","MESH:C564071","UMLS:C1839413","GARD:4620","ICD9:277.6","OMIM:312170"],"synonyms":[{"name":"PDH deficiency","type":"related"},{"name":"PDHAD","type":"exact"},{"name":"ataxia with lactic acidosis 1","type":"related"},{"name":"ataxia, intermittent, with abnormal pyruvate metabolism","type":"related"},{"name":"ataxia, intermittent, with pyruvate dehydrogenase deficiency","type":"related"},{"name":"ataxia, intermittent, with pyruvate dehydrogenase, or decarboxylase, deficiency","type":"related"},{"name":"lactic acidemia, thiamine-responsive","type":"related"},{"name":"pyruvate decarboxylase deficiency","type":"broad"},{"name":"pyruvate dehydrogenase Complex deficiency","type":"related"},{"name":"pyruvate dehydrogenase E1-ALPHA deficiency","type":"related"},{"name":"pyruvate dehydrogenase E1-alpha deficiency","type":"exact"},{"name":"pyruvate dehydrogenase complex E1 component subunit alpha deficiency","type":"exact"},{"name":"pyruvate dehydrogenase e1-alpha deficiency, X-linked dominant","type":"exact"}],"termid":"MONDO:0010717","terms_by_termid":{"MONDO:0010717":null},"xrefs":{"Monarch":{"xref_id":"0010717"}}}


id: MONDO:0006644
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder of the liver characterized by the presence of fibrotic scar tissue instead of healthy liver tissue. This condition is attributed to excessive consumption of alcoholic beverages.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cirrhosis of liver","termid":"MONDO:0005155"},{"relation_name":"is_a","term_name":"alcoholic liver diseases","termid":"MONDO:0043693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"alcoholic liver cirrhosis","secondary_identifiers":["CSP:1754-7677","UMLS:C0023891","DOID:14018","EFO:1000802","ICD10CM:K70.3","ICD9:571.2","NCIT:C34782","MEDGEN:6125","MedDRA:10001618","SCTID:419728003","MESH:D008104"],"synonyms":[{"name":"Laennec's cirrhosis","type":"related"},{"name":"Laennec's cirrhosis, alcoholic","type":"related"},{"name":"alcoholic cirrhosis","type":"exact"},{"name":"alcoholic cirrhosis of liver","type":"exact"},{"name":"portal cirrhosis","type":"related"}],"termid":"MONDO:0006644","xrefs":{"Monarch":{"xref_id":"0006644"}}}


id: MONDO:0032592
data:
  {"annotated_genes":["SJAG_01139"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86596],"is_not":false,"summary":null,"term":"MONDO:0032592"}]},"cv_name":"mondo","definition":"A dilated cardiomyopathy that is characterized by dilated cardiomyopathy of variable severity, with age of onset ranging from 2 to 20 years and that has material basis in homozygous or compound heterozygous mutation in the PPCS gene on chromosome 1p34.","definition_xrefs":["DOID:0081159"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01139":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiomyopathy, dilated, 2c","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1648379","OMIM:618189","UMLS:C4748647","GARD:16305"],"synonyms":[{"name":"CARDIOMYOPATHY, DILATED, 2C","type":"related"},{"name":"CMD2C","type":"related"}],"termid":"MONDO:0032592","terms_by_termid":{"MONDO:0032592":null},"xrefs":{"Monarch":{"xref_id":"0032592"}}}


id: MONDO:0007379
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Meesmann corneal dystrophy (MECD) is a rare form of superficial corneal dystrophy characterized by distinct tiny bubble-like, round-to-oval punctate bilateral opacities in the central corneal epithelium, and to a lesser extent in the peripheral cornea, with little impact on vision.","definition_xrefs":["Orphanet:98954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial and subepithelial corneal dystrophy","termid":"MONDO:0000763"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"superficial corneal dystrophy","termid":"MONDO:0020212"}],"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":"Meesmann corneal dystrophy","secondary_identifiers":["NCIT:C84795","DOID:0060451","GARD:9688","ICD9:371.51","MEDGEN:83283","MESH:D053559","OMIMPS:122100","SCTID:1674008","UMLS:C0339277"],"synonyms":[{"name":"MECD","type":"exact"},{"name":"Meesman dystrophy","type":"related"},{"name":"Meesmann corneal dystrophy","type":"exact"},{"name":"Meesmann corneal epithelial dystrophy","type":"related"},{"name":"corneal dystrophy, Meesmann","type":"related"},{"name":"corneal dystrophy, Meesmann epithelial","type":"related"},{"name":"corneal dystrophy, juvenile epithelial of Meesmann","type":"related"},{"name":"corneal dystrophy, juvenile epithelial, of Meesmann","type":"related"},{"name":"juvenile epithelial of Meesmann corneal dystrophy","type":"exact"},{"name":"juvenile hereditary epithelial dystrophy","type":"exact"},{"name":"juvenile hereditary epithelial dystrophy of Meesmann","type":"exact"},{"name":"stocker-Holt dystrophy","type":"exact"}],"termid":"MONDO:0007379","xrefs":{"Monarch":{"xref_id":"0007379"}}}


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


id: MONDO:1011694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"thrombasthenia, non-human animal","secondary_identifiers":["OMIA:001000"],"termid":"MONDO:1011694","xrefs":{"Monarch":{"xref_id":"1011694"}}}


id: GO:0004286
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the release of protein hormones and neuropeptides from their precursors, generally by cleavage of -Lys-Arg-Xaa at the Arg-Xaa bond.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete proprotein convertase 2 activity (obsolete GO:0004286)","synonyms":[{"name":"NEC 2 activity","type":"narrow"},{"name":"PC2 activity","type":"narrow"},{"name":"neuroendocrine convertase 2 activity","type":"narrow"},{"name":"prohormone convertase II activity","type":"narrow"},{"name":"proprotein convertase 2 activity","type":"exact"}],"termid":"GO:0004286"}


id: PBO:0078659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon CTT) 12-1","termid":"PBO:0078659"}


id: GO:1900797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving cordyol C.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catechol-containing compound metabolic process","termid":"GO:0009712"},{"relation_name":"is_a","term_name":"ether metabolic process","termid":"GO:0018904"},{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0019748","GO:0008150"],"is_obsolete":false,"name":"cordyol C metabolic process","synonyms":[{"name":"cordyol C metabolism","type":"exact"}],"termid":"GO:1900797"}


id: MONDO:0016030
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Evans syndrome is a rare chronic hematologic disorder characterized by the simultaneous or sequential association of autoimmune hemolytic anemia (AIHA; a disorder in which auto-antibodies are directed against red blood cells causing anemia of varying degrees of severity) with immune thrombocytopenic purpura (ITP; a coagulation disorder in which auto-antibodies are directed against platelets causing hemorrhagic episodes) and occasionally autoimmune neutropenia, in the absence of a known underlying etiology.","definition_xrefs":["Orphanet:1959"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"primary thrombocytopenia","termid":"MONDO:0004680"},{"relation_name":"is_a","term_name":"autoimmune thrombocytopenia","termid":"MONDO:0019098"},{"relation_name":"is_a","term_name":"autoimmune hemolytic anemia","termid":"MONDO:0020108"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"Evans syndrome","secondary_identifiers":["ICD10CM:D69.41","GARD:6389","ICD9:287.32","MESH:C536380","SCTID:75331009","NANDO:1200310","MedDRA:10053873","icd11.foundation:1048228553","MEDGEN:75773","NCIT:C61284","UMLS:C0272126","NORD:1112","DOID:8931"],"synonyms":[{"name":"Evan syndrome","type":"related"},{"name":"Evans' syndrome","type":"exact"},{"name":"autoimmune hemolytic anaemia and autoimmune thrombocytopenia","type":"exact"},{"name":"autoimmune hemolytic anemia and autoimmune thrombocytopenia","type":"exact"},{"name":"immune pancytopenia","type":"exact"}],"termid":"MONDO:0016030","xrefs":{"Monarch":{"xref_id":"0016030"}}}


id: GO:0071836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of a nectar by a cell or a tissue. Nectar is a fluid secreted by many angiosperms to promote pollination by providing a reward to pollinators. Nectar may also deter certain organisms from visiting or play other biological roles. Nectar is a complex solution that may include the following types of compounds: sugars, amino acids, organic acids, alkaloids, flavonoids, glycosides, vitamins, phenolics, metal ions, oils, free fatty acids, and proteins.","definition_xrefs":["PMID:19861655","GOC:kad"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretion","termid":"GO:0046903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"nectar secretion","synonyms":[{"name":"nectar production","type":"related"}],"termid":"GO:0071836"}


id: MONDO:0012188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuronal ceroid lipofuscinosis 9 (CLN9-NCL) is a rare condition that affects the nervous system. Signs and symptoms of the condition generally develop in early childhood (average age 4 years) and may include loss of muscle coordination (ataxia), seizures that do not respond to medications, muscle twitches (myoclonus), visual impairment, and developmental regression (the loss of previously acquired skills). The underlying genetic cause of CLN9-NCLis unknown but it appears to be inherited in an autosomal recessive manner. Treatment options are limited to therapies that can help relieve some of the symptoms.","direct_ancestors":[{"relation_name":"is_a","term_name":"juvenile neuronal ceroid lipofuscinosis","termid":"MONDO:0019262"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005559","MONDO:0002561","MONDO:0002039","MONDO:0005066"],"is_obsolete":false,"name":"neuronal ceroid lipofuscinosis 9","secondary_identifiers":["MEDGEN:332304","Orphanet:228357","UMLS:C1836841","DOID:0110733","GARD:6618","MESH:C537953","OMIM:609055"],"synonyms":[{"name":"CLN 9","type":"related"},{"name":"CLN9","type":"exact"},{"name":"CLN9 disease","type":"related"},{"name":"ceroid lipofuscinosis, neuronal, 9","type":"related"},{"name":"neuronal ceroid lipofuscinosis type 9","type":"exact"}],"termid":"MONDO:0012188","xrefs":{"Monarch":{"xref_id":"0012188"}}}


id: PBO:0052517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLHL30 antisense RNA 1","termid":"PBO:0052517"}


id: PBO:0078312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asp (GTC) 8-1","termid":"PBO:0078312"}


id: PBO:0005699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L27 (predicted)","termid":"PBO:0005699"}


id: GO:0120239
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The carbohydrate-rich layer lining the vascular endothelium connected to the endothelium through a variety of molecules, mainly proteoglycans and glycoproteins. These form a network in which soluble molecules, either plasma- or endothelium-derived, are incorporated.","definition_xrefs":["GOC:krc","PMID:17256154"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycocalyx","termid":"GO:0030112"}],"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":"vascular endothelial glycocalyx","synonyms":[{"name":"endothelial glycocalyx","type":"exact"}],"termid":"GO:0120239"}


id: FYPO:0002844
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which a cell undergoes one or a few rounds of cell division before cells die, resulting in the formation a colony that contains only a few inviable cells which are septated, elongated, and have a larger than normal cell volume. Up to 6 rounds of cell division (generating 64 cells) may be observed, but 3 divisions or fewer is more typical.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable microcolony, swollen elongated septated cells (obsolete FYPO:0002844)","synonyms":[{"name":"inviable microcolony, enlarged long septated vegetative cells","type":"related"},{"name":"inviable microcolony, large elongated septated vegetative cells","type":"related"},{"name":"inviable microcolony, swollen elongated septated vegetative cells","type":"exact"}],"termid":"FYPO:0002844"}


id: SO:0000704
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region (or regions) that includes all of the sequence elements necessary to encode a functional transcript. A gene may include regulatory regions, transcribed regions and/or other functional sequence regions.","definition_xrefs":["SO:immuno_workshop"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"},{"relation_name":"member_of","term_name":"gene_group","termid":"SO:0005855"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene","secondary_identifiers":["http://en.wikipedia.org/wiki/Gene"],"synonyms":[{"name":"INSDC_feature:gene","type":"exact"}],"termid":"SO:0000704"}


id: FYPO:0004737
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the amount of filamentous actin (F-actin) in the actomyosin contractile ring is lower than normal during early mitosis (before anaphase).","definition_xrefs":["PMID:25688133","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring","termid":"FYPO:0004736"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0004803","FYPO:0000631","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased F-actin level in actomyosin contractile ring during early mitosis","synonyms":[{"name":"decreased F-actin level in actomyosin contractile ring during early mitosis during mitotic cell cycle","type":"related"},{"name":"decreased F-actin level in actomyosin contractile ring during early mitosis during vegetative growth","type":"exact"},{"name":"decreased F-actin level in mitotic contractile ring during early mitosis","type":"exact"},{"name":"decreased abundance of F-actin in the actomyosin contractile ring in early mitosis","type":"exact"},{"name":"decreased actomyosin contractile ring F-actin level during early mitosis","type":"exact"},{"name":"decreased filamentous actin level in actomyosin contractile ring during early mitosis","type":"exact"}],"termid":"FYPO:0004737"}


id: PBO:0067369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 470, pseudogene","termid":"PBO:0067369"}


id: PBO:0029752
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_modification","termid":"PBO:0029752"}


id: GO:0001095
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a general RNA polymerase II transcription factor belonging to the TFIIE complex, one of the factors involved in formation of the preinitiation complex (PIC) by RNA polymerase II.","definition_xrefs":["GOC:krc","PMID:16858867"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II general transcription initiation factor binding","termid":"GO:0001091"},{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"TFIIE-class transcription factor complex binding","synonyms":[{"name":"TFIIE-class transcription factor binding","type":"exact"}],"termid":"GO:0001095"}


id: PBO:0063062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pantothenate kinase 2","termid":"PBO:0063062"}


id: GO:1902126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (+)-pinoresinol.","definition_xrefs":["GOC:TermGenie","PMID:8910615","PMID:9872995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan biosynthetic process","termid":"GO:0009807"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"ether biosynthetic process","termid":"GO:1901503"},{"relation_name":"is_a","term_name":"(+)-pinoresinol metabolic process","termid":"GO:1902124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"(+)-pinoresinol biosynthetic process","synonyms":[{"name":"(+)-pinoresinol anabolism","type":"exact"},{"name":"(+)-pinoresinol biosynthesis","type":"exact"},{"name":"(+)-pinoresinol formation","type":"exact"},{"name":"(+)-pinoresinol synthesis","type":"exact"}],"termid":"GO:1902126"}


id: PBO:0064142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PKN2 antisense RNA 1","termid":"PBO:0064142"}


id: PBO:0000280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fen1 family nuclease, XP-G family (predicted)","termid":"PBO:0000280"}


id: FYECO:0000092
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which sodium ions were added to the assay buffer in excess compared to standard assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ ions","termid":"FYECO:0000030"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ Na ions","synonyms":[{"name":"sodium ions added","type":"exact"}],"termid":"FYECO:0000092"}


id: GO:0031718
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1 cannabinoid receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cannabinoid receptor binding","termid":"GO:0031717"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"type 1 cannabinoid receptor binding","synonyms":[{"name":"type 1 cannabinoid receptor ligand","type":"narrow"}],"termid":"GO:0031718"}


id: MONDO:0044276
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete skin/hair/eye pigmentation, variation in, 11 (obsolete MONDO:0044276)","secondary_identifiers":["OMIM:612271"],"synonyms":[{"name":"Melanesian blond hair","type":"related"},{"name":"SHEP11","type":"related"},{"name":"skin/hair/eye pigmentation 11, blue/Nonblue eyes","type":"related"},{"name":"skin/hair/eye pigmentation, variation IN, 11","type":"related"},{"name":"skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)","type":"exact"}],"termid":"MONDO:0044276","xrefs":{"Monarch":{"xref_id":"0044276"}}}


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:0012641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"restless legs syndrome, susceptibility to","termid":"MONDO:0100170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restless legs syndrome, susceptibility to, 5","secondary_identifiers":["MEDGEN:370807","UMLS:C1970010","OMIM:611242"],"synonyms":[{"name":"RLS 5","type":"related"},{"name":"RLS5","type":"exact"},{"name":"restless legs syndrome 5","type":"exact"},{"name":"restless legs syndrome, susceptibility to, 5","type":"exact"}],"termid":"MONDO:0012641","xrefs":{"Monarch":{"xref_id":"0012641"}}}


id: PBO:0059103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MORF4L2 antisense RNA 1","termid":"PBO:0059103"}


id: GO:0019821
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A subform of peroxisome that corresponds to an intermediate in a peroxisome assembly pathway, which operates by conversion of peroxisomal subforms in the direction P1, P2 -> P3 -> P4 -> P5 -> P6. P3 peroxisomes are formed by fusion of P1 and P2 peroxisomes, and are distinguished from the other subforms on the bases of buoyant density and protein content.","definition_xrefs":["PMID:10629216"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisome","termid":"GO:0005777"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005777"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005777","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"P3 peroxisome","synonyms":[{"name":"peroxisome vesicle","type":"broad"}],"termid":"GO:0019821"}


id: GO:0060957
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of a cell to an endocardial cell fate and its capacity to differentiate into an endocardial cell. An endocardial cell is a specialized endothelial cell that makes up the endocardium portion of the heart.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell fate commitment","termid":"GO:0060839"},{"relation_name":"is_a","term_name":"cardiac cell fate commitment","termid":"GO:0060911"},{"relation_name":"part_of","term_name":"endocardial cell differentiation","termid":"GO:0060956"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"endocardial cell fate commitment","termid":"GO:0060957"}


id: GO:1903210
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process in a glomerular visceral epithelial cell.","definition_xrefs":["PMID:23515840","GOC:TermGenie","GO_REF:0000085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell apoptotic process","termid":"GO:1904019"}],"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":"podocyte apoptotic process","synonyms":[{"name":"glomerular podocyte apoptosis","type":"narrow"},{"name":"glomerular podocyte apoptotic process","type":"exact"},{"name":"glomerular visceral epithelial cell apoptosis","type":"narrow"},{"name":"glomerular visceral epithelial cell apoptotic process","type":"exact"},{"name":"podocyte apoptosis","type":"narrow"}],"termid":"GO:1903210"}


id: PBO:0060042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 30","termid":"PBO:0060042"}


id: PBO:0055815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipin 3","termid":"PBO:0055815"}


id: GO:1903903
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of establishment of T cell polarity.","definition_xrefs":["PMID:23575248","GO_REF:0000058","GOC:als","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of establishment of cell polarity","termid":"GO:2000114"},{"relation_name":"regulates","term_name":"establishment of T cell polarity","termid":"GO:0001768"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"regulation of establishment of T cell polarity","synonyms":[{"name":"regulation of T cell polarization","type":"exact"},{"name":"regulation of T lymphocyte polarization","type":"exact"},{"name":"regulation of T-cell polarization","type":"exact"},{"name":"regulation of establishment of T lymphocyte polarity","type":"exact"},{"name":"regulation of establishment of T-cell polarity","type":"exact"},{"name":"regulation of establishment of T-lymphocyte polarity","type":"exact"}],"termid":"GO:1903903"}


id: PBO:0065830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB6D, member RAS oncogene family","termid":"PBO:0065830"}


id: _global:contributes_to
data:
  {"annotation_feature_type":"gene","cv_name":"external","direct_ancestors":[{"relation_name":"is_a","term_name":"capable_of_part_of","termid":"_global:capable_of_part_of"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"},{"relation_name":"is_a","term_name":"part_of_structure_that_is_capable_of","termid":"_global:part_of_structure_that_is_capable_of"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contributes_to","secondary_identifiers":["RO:0002326"],"termid":"_global:contributes_to"}


id: PBO:0053459
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 412","termid":"PBO:0053459"}


id: PBO:0045156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal heavy chain 11","termid":"PBO:0045156"}


id: PBO:0074769
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 3B-2","termid":"PBO:0074769"}


id: GO:0007160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The binding of a cell to the extracellular matrix via adhesion molecules.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-substrate adhesion","termid":"GO:0031589"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"cell-matrix adhesion","termid":"GO:0007160"}


id: PBO:0075998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STEAP4 metalloreductase","termid":"PBO:0075998"}


id: PATO:0000148
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000148 body temperature (obsolete PATO:0000148)","termid":"PATO:0000148"}


id: GO:0106267
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (3-chloro-2,4,6-trihydroxyphenyl)hexan-1-one + chloride + FADH2 + O2 = (3,5-dichloro-2,4,6-trihydroxyphenyl)hexan-1-one + FAD + 2 H2O.","definition_xrefs":["PMID:20231486","RHEA:64360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"3,5 dichloro-THPH synthase activity","termid":"GO:0106267"}


id: MONDO:0032770
data:
  {"annotated_genes":["SJAG_03579","SJAG_02869","SJAG_01016"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87488,87489,87490],"is_not":false,"summary":null,"term":"MONDO:0032770"}]},"cv_name":"mondo","definition":"Any BAFopathy in which the cause of the disease is a mutation in the ACTL6B gene.","definition_xrefs":["MONDO:patterns/OMIM_disease_series_by_gene","PMID:30580808"],"direct_ancestors":[{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01016":null,"SJAG_02869":null,"SJAG_03579":null},"genotype_count":0,"is_obsolete":false,"name":"intellectual developmental disorder with severe speech and ambulation defects","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5193115","MEDGEN:1682234","GARD:18518","OMIM:618470"],"synonyms":[{"name":"ACTL6B-related BAFopathy","type":"exact"},{"name":"IDDSSAD","type":"related"},{"name":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS","type":"related"}],"termid":"MONDO:0032770","terms_by_termid":{"MONDO:0032770":null},"xrefs":{"Monarch":{"xref_id":"0032770"}}}


id: PBO:0083937
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Galactose-1-phosphate uridyl transferase; synthesizes glucose-1-phosphate and UDP-galactose from UDP-D-glucose and alpha-D-galactose-1-phosphate in the second step of galactose catabolism; human homolog UGP2 can complement yeast null mutant","termid":"PBO:0083937"}


id: PBO:0028828
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_RNA_localization_to_chromatin","termid":"PBO:0028828"}


id: PBO:0090688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial lysine-tRNA ligase Msk1","termid":"PBO:0090688"}


id: PBO:0004470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L18","termid":"PBO:0004470"}


id: PBO:0081237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 3","termid":"PBO:0081237"}


id: FYPO:0003729
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a protein that is not normally found in the nuclear periphery is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein mislocalized to nucleus during vegetative growth","termid":"FYPO:0000784"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"protein mislocalized to nuclear periphery","synonyms":[{"name":"ectopic protein localization to nuclear periphery","type":"exact"},{"name":"protein mislocalised to nuclear periphery","type":"exact"},{"name":"protein mislocalised to nuclear periphery during vegetative growth","type":"exact"},{"name":"protein mislocalized to nuclear periphery during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003729"}


id: PBO:0050706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSPB2-C11orf52 readthrough (NMD candidate)","termid":"PBO:0050706"}


id: MONDO:0017828
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary renal tubular acidosis (obsolete MONDO:0017828)","secondary_identifiers":["Orphanet:314822"],"termid":"MONDO:0017828","xrefs":{"Monarch":{"xref_id":"0017828"}}}


id: PBO:0070233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 171 pseudogene","termid":"PBO:0070233"}


id: MONDO:0100109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare condition comprising a triad of unilateral renal agenesis, ipsilateral seminal vesicle obstruction and ipsilateral ejaculatory duct obstruction.","definition_xrefs":["PMID:30258511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinner syndrome","termid":"MONDO:0100109","xrefs":{"Monarch":{"xref_id":"0100109"}}}


id: PBO:0036055
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_duration_of_mitotic_anaphase_B","termid":"PBO:0036055"}


id: PBO:0062165
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 K member 6 pseudogene","termid":"PBO:0062165"}


id: PBO:0045550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 5","termid":"PBO:0045550"}


id: GO:2000961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellooligosaccharide metabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"regulation of cellooligosaccharide metabolic process","termid":"GO:2000960"},{"relation_name":"negatively_regulates","term_name":"cellooligosaccharide metabolic process","termid":"GO:2000902"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cellooligosaccharide metabolic process","synonyms":[{"name":"negative regulation of cellooligosaccharide metabolism","type":"exact"}],"termid":"GO:2000961"}


id: PBO:0041806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase recruitment domain family member 17, pseudogene","termid":"PBO:0041806"}


id: MONDO:0022519
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune myocarditis is an autoimmune disease that affects the heart. The condition is characterized by inflammation of the heart muscle (myocardium). Some people with autoimmune myocarditis have no noticeable symptoms of the condition. When present, signs and symptoms may include chest pain, abnormal heartbeat, shortness of breath, fatigue, signs of infection (i.e. fever, headache, sore throat, diarrhea), and leg swelling. The exact underlying cause of the condition is currently unknown; however, autoimmune conditions, in general, occur when the immune system mistakenly attacks healthy tissue. Treatment is based on the signs and symptoms present in each person. In some cases, medications that suppress the immune system may be recommended.","definition_xrefs":["GARD:0009519"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myocarditis","termid":"MONDO:0004496"},{"relation_name":"is_a","term_name":"autoimmune cardiomyopathy","termid":"MONDO:0030701"}],"gene_count":0,"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":"autoimmune myocarditis","secondary_identifiers":["DOID:0080767","GARD:9519","UMLS:C1608389","MEDGEN:299070"],"termid":"MONDO:0022519","xrefs":{"Monarch":{"xref_id":"0022519"}}}


id: PBO:0091002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome-associated signalling scaffold, receptor of activated C kinase (RACK1) ortholog Cpc2","termid":"PBO:0091002"}


id: PBO:0057061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 145","termid":"PBO:0057061"}


id: PBO:0043982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CSE1L divergent transcript","termid":"PBO:0043982"}


id: SO:0001549
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variant that changes alters the transcription of a transcript with respect to a reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_function_variant","termid":"SO:0001538"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription_variant","synonyms":[{"name":"transcription variant","type":"exact"}],"termid":"SO:0001549"}


id: MONDO:0004452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germinoma arising from the central nervous system during childhood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system germinoma","termid":"MONDO:0002999"},{"relation_name":"is_a","term_name":"childhood central nervous system germ cell tumor","termid":"MONDO:0003750"},{"relation_name":"is_a","term_name":"malignant childhood germ cell neoplasm","termid":"MONDO:0004479"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"childhood central nervous system germinoma","secondary_identifiers":["MEDGEN:272460","NCIT:C27406","DOID:8078","UMLS:C1332953"],"synonyms":[{"name":"Central nervous system germinoma","type":"broad"},{"name":"central nervous system germinoma of childhood","type":"exact"},{"name":"paediatric central nervous system germinoma","type":"exact"},{"name":"pediatric central nervous system germinoma","type":"exact"}],"termid":"MONDO:0004452","xrefs":{"Monarch":{"xref_id":"0004452"}}}


id: PBO:0070959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18a pseudogene 14","termid":"PBO:0070959"}


id: PBO:0029087
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_tRNA_(guanine(9)-N(1))-methyltransferase_activity","termid":"PBO:0029087"}


id: PBO:0070347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY4 pseudogene 20","termid":"PBO:0070347"}


id: PR:Q9Y7P0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A riboflavin synthase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04809"],"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":"riboflavin synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1450.13c","secondary_identifiers":["UniProtKB:Q9Y7P0"],"synonyms":[{"name":"RS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ribC","type":"exact"}],"termid":"PR:Q9Y7P0"}


id: PBO:0004149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF757 family protein","termid":"PBO:0004149"}


id: PBO:0067766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 66","termid":"PBO:0067766"}


id: MONDO:0009034
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Craniofacial dyssynostosis (CFD) is a rare cranial malformation syndrome characterized by the premature closure of both lambdoid sutures and the posterior sagittal suture, resulting in abnormal skull contour (frontal bossing, anterior turricephaly with mild brachycephaly, biparietal narrowing, occipital concavity) and dysmorphic facial features (low-set ears, midfacial hypoplasia). Short stature, developmental delay, epilepsy, and oculomotor dyspraxia have also been reported. Associated anomalies include enlargement of the cerebral ventricles, agenesis of the corpus callosum, Arnold-Chiari malformation type I, venous anomalies of skull and hydrocephalus.","definition_xrefs":["Orphanet:1516"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"craniofacial dyssynostosis","secondary_identifiers":["GARD:1575","MESH:C536455","OMIM:218350","UMLS:C1857511","MEDGEN:347473"],"synonyms":[{"name":"bilateral lambdoid and sagittal synostosis","type":"related"},{"name":"craniofacial dyssynostosis and short stature","type":"related"},{"name":"craniofacial dyssynostosis with short stature","type":"related"},{"name":"craniosynostosis-craniofacial dysostosis syndrome","type":"related"}],"termid":"MONDO:0009034","xrefs":{"Monarch":{"xref_id":"0009034"}}}


id: FYPO:0003355
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"Auxotrophy in which a cell is unable to synthesize sulfur-containing amino acids, and therefore requires one or more sulfur-containing amino acids (e.g. cysteine or methionine) in the medium for vegetative cell growth.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxotrophy","termid":"FYPO:0000128"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype","termid":"FYPO:0004638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"growth auxotrophic for sulfur-containing amino acid","synonyms":[{"name":"growth auxotrophic for sulfur-containing amino acid during mitotic cell cycle","type":"related"},{"name":"growth auxotrophic for sulfur-containing amino acid during vegetative growth","type":"exact"},{"name":"growth auxotrophic for sulphur-containing amino acid","type":"exact"},{"name":"sulfur-containing amino acid auxotrophy","type":"exact"}],"termid":"FYPO:0003355"}


id: GO:0035060
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SWI/SNF-type complex that contains 8 to 14 proteins, including both conserved (core) and nonconserved components; contains the ATPase product of the Drosophila brm (brahma) or mammalian SMARCA2/BAF190B/BRM gene, or an ortholog thereof.","definition_xrefs":["GOC:bhm","PMID:10809665","PMID:12482982"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SWI/SNF superfamily-type complex","termid":"GO:0070603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0005575","GO:0005634","GO:0032991"],"is_obsolete":false,"name":"brahma complex","synonyms":[{"name":"BRM complex","type":"exact"}],"termid":"GO:0035060"}


id: PBO:0055192
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 2616","termid":"PBO:0055192"}


id: GO:1905154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of membrane invagination.","definition_xrefs":["GO_REF:0000058","GOC:bf","GOC:PARL","GOC:TermGenie","PMID:26589353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"is_a","term_name":"regulation of membrane invagination","termid":"GO:1905153"},{"relation_name":"negatively_regulates","term_name":"membrane invagination","termid":"GO:0010324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"negatively_regulates","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"negative regulation of membrane invagination","synonyms":[{"name":"down regulation of membrane invagination","type":"exact"},{"name":"down-regulation of membrane invagination","type":"exact"},{"name":"downregulation of membrane invagination","type":"exact"},{"name":"inhibition of membrane invagination","type":"narrow"}],"termid":"GO:1905154"}


id: PBO:0071000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 2","termid":"PBO:0071000"}


id: FYPO:0001949
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 calcium ion measured in the cytosol is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular calcium level","termid":"FYPO:0001198"},{"relation_name":"is_a","term_name":"increased level of substance in cytosol","termid":"FYPO:0001948"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cytosolic calcium level","synonyms":[{"name":"increased cytosolic calcium ion level","type":"exact"},{"name":"increased cytosolic calcium ion level during vegetative growth","type":"exact"},{"name":"increased cytosolic calcium level during mitotic cell cycle","type":"related"},{"name":"increased level of calcium ions in cytosol","type":"exact"},{"name":"increased levels of free cytosolic calcium","type":"exact"}],"termid":"FYPO:0001949"}


id: PBO:0049619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 22","termid":"PBO:0049619"}


id: PBO:0058176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4471","termid":"PBO:0058176"}


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


id: MONDO:0013171
data:
  {"annotated_genes":["SJAG_01359"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86811],"is_not":false,"summary":null,"term":"MONDO:0013171"}]},"cv_name":"mondo","definition":"Purine nucleoside phosphorylase (PNP) deficiency is a disorder of purine metabolism characterized by progressive immunodeficiency leading to recurrent and opportunistic infections, autoimmunity and malignancy as well as neurologic manifestations.","definition_xrefs":["Orphanet:760"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"severe combined immunodeficiency","termid":"MONDO:0015974"},{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"inborn disorder of purine metabolism","termid":"MONDO:0019236"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01359":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019254"}],"interesting_parent_ids":["MONDO:0019254","MONDO:0005066"],"is_obsolete":false,"name":"purine nucleoside phosphorylase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:5813","NANDO:2200698","OMIM:613179","SCTID:60743005","ICD9:277.2","MESH:C562587","HGNC:7892","GARD:4606","MEDGEN:75653","NANDO:1200325","NCIT:C176817","NCIT:C3963","UMLS:C0268125"],"synonyms":[{"name":"PNP deficiency","type":"exact"},{"name":"PNPase deficiency","type":"exact"},{"name":"deficiency of inosine phosphorylase","type":"exact"},{"name":"immunodeficiency due to purine nucleoside phosphorylase deficiency","type":"exact"},{"name":"nucleoside phosphorylase deficiency","type":"related"},{"name":"purine nucleoside phosphorylase deficiency","type":"exact"},{"name":"purine-nucleoside phosphorylase deficiency","type":"exact"}],"termid":"MONDO:0013171","terms_by_termid":{"MONDO:0013171":null},"xrefs":{"Monarch":{"xref_id":"0013171"}}}


id: PBO:0001465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosine-mismatch binding protein 1","termid":"PBO:0001465"}


id: PBO:0052572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine methyltransferase 5A","termid":"PBO:0052572"}


id: PBO:0027329
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_translation_of_ribosomal_proteins","termid":"PBO:0027329"}


id: PBO:0047166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 193 member B","termid":"PBO:0047166"}


id: FYPO:0006760
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which centromeres do not detach properly from the spindle pole body (SPB) during the meiotic cell cycle. Normally, centromeres are located at the SPB during mitotic interphase, and upon entering meiosis, telomeres cluster at the SPB, followed by centromere detachment from the SPB.","definition_xrefs":["PMID:27611693","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic chromosome organization","termid":"FYPO:0006759"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000631","FYPO:0000641"],"is_obsolete":false,"name":"abnormal centromere detachment from spindle pole body during meiotic chromosome organization","synonyms":[{"name":"abnormal centromere detachment from SPB during meiotic chromosome organization","type":"exact"},{"name":"abnormal centromere detachment from spindle pole body during meiotic chromosome organisation","type":"exact"},{"name":"abnormal centromere detachment from spindle pole body involved in chromosome organization involved in meiotic cell cycle","type":"exact"},{"name":"abnormal centromere detachment from spindle pole body involved in meiotic chromosome organization","type":"exact"},{"name":"defective centromere detachment from the SPB during karyogamy and meiotic prophase","type":"exact"}],"termid":"FYPO:0006760"}


id: GO:1905170
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein localization to phagocytic vesicle.","definition_xrefs":["GO_REF:0000058","GOC:bf","GOC:TermGenie","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein localization","termid":"GO:1903828"},{"relation_name":"is_a","term_name":"regulation of protein localization to phagocytic vesicle","termid":"GO:1905169"},{"relation_name":"negatively_regulates","term_name":"protein localization to phagocytic vesicle","termid":"GO:1905161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein localization to phagocytic vesicle","synonyms":[{"name":"down regulation of protein localisation in phagocytic vesicle","type":"exact"},{"name":"down regulation of protein localisation to phagocytic vesicle","type":"exact"},{"name":"down regulation of protein localisation to phagosome","type":"exact"},{"name":"down regulation of protein localization in phagocytic vesicle","type":"exact"},{"name":"down regulation of protein localization to phagocytic vesicle","type":"exact"},{"name":"down regulation of protein recruitment to phagosome","type":"exact"},{"name":"down-regulation of protein localisation in phagocytic vesicle","type":"exact"},{"name":"down-regulation of protein localisation to phagocytic vesicle","type":"exact"},{"name":"down-regulation of protein localisation to phagosome","type":"exact"},{"name":"down-regulation of protein localization in phagocytic vesicle","type":"exact"},{"name":"down-regulation of protein localization to phagocytic vesicle","type":"exact"},{"name":"down-regulation of protein recruitment to phagosome","type":"exact"},{"name":"downregulation of protein localisation in phagocytic vesicle","type":"exact"},{"name":"downregulation of protein localisation to phagocytic vesicle","type":"exact"},{"name":"downregulation of protein localisation to phagosome","type":"exact"},{"name":"downregulation of protein localization in phagocytic vesicle","type":"exact"},{"name":"downregulation of protein localization to phagocytic vesicle","type":"exact"},{"name":"downregulation of protein recruitment to phagosome","type":"exact"},{"name":"inhibition of protein localisation in phagocytic vesicle","type":"narrow"},{"name":"inhibition of protein localisation to phagocytic vesicle","type":"narrow"},{"name":"inhibition of protein localisation to phagosome","type":"narrow"},{"name":"inhibition of protein localization in phagocytic vesicle","type":"narrow"},{"name":"inhibition of protein localization to phagocytic vesicle","type":"narrow"},{"name":"inhibition of protein recruitment to phagosome","type":"narrow"},{"name":"negative regulation of protein localisation in phagocytic vesicle","type":"exact"},{"name":"negative regulation of protein localisation to phagocytic vesicle","type":"exact"},{"name":"negative regulation of protein localisation to phagosome","type":"exact"},{"name":"negative regulation of protein localization in phagocytic vesicle","type":"exact"},{"name":"negative regulation of protein recruitment to phagosome","type":"exact"}],"termid":"GO:1905170"}


id: MONDO:0003534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare primary thymic adenocarcinoma, characterized by a papillary growth pattern. There are only a few published cases, and no good data regarding prognosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary adenocarcinoma","termid":"MONDO:0002512"},{"relation_name":"is_a","term_name":"thymus gland adenocarcinoma","termid":"MONDO:0003209"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"papillary thymic adenocarcinoma","secondary_identifiers":["NCIT:C27937","DOID:5595","UMLS:C1335327","MEDGEN:233836"],"synonyms":[{"name":"Thymus papillary carcinoma","type":"exact"},{"name":"papillary carcinoma of Thymus","type":"exact"},{"name":"papillary carcinoma of the Thymus","type":"exact"},{"name":"thymic papillary adenocarcinoma","type":"exact"},{"name":"thymic papillary carcinoma","type":"exact"},{"name":"thymus papillary adenocarcinoma","type":"exact"}],"termid":"MONDO:0003534","xrefs":{"Monarch":{"xref_id":"0003534"}}}


id: PR:O43125
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- lsb1 gene.","definition_xrefs":["UniProtKB:O43125","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":"protein csh3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC119.05c","synonyms":[{"name":"Spom972h-lsb1","type":"exact"}],"termid":"PR:O43125"}


id: MONDO:0015885
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A cluster of closely related metabolic abnormalities associated with insulin resistance that confer an increased risk of the development of type 2 diabetes and cardiovascular disease. These abnormalities may include obesity, high blood pressure, abnormal cholesterol levels, proteinuria, and/or polycystic ovary syndrome.","definition_xrefs":["NCIT:C113169"],"gene_count":0,"genotype_count":0,"name":"obsolete rare insulin-resistance syndrome (obsolete MONDO:0015885)","secondary_identifiers":["Orphanet:181368"],"synonyms":[{"name":"insulin Resistance syndrome","type":"exact"}],"termid":"MONDO:0015885","xrefs":{"Monarch":{"xref_id":"0015885"}}}


id: PBO:0045695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein light chain Tctex-type 2B","termid":"PBO:0045695"}


id: GO:1903808
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of L-tyrosine from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:TermGenie","PMID:23895341","GO_REF:0000075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tyrosine transport","termid":"GO:0015828"},{"relation_name":"is_a","term_name":"amino acid import across plasma membrane","termid":"GO:0089718"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"}],"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"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"L-tyrosine import across plasma membrane","secondary_identifiers":["GO:0036232"],"synonyms":[{"name":"L-tyrosine import","type":"broad"},{"name":"L-tyrosine import into cell","type":"exact"},{"name":"L-tyrosine uptake","type":"exact"}],"termid":"GO:1903808"}


id: GO:0050407
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: [glycogen-synthase D] + H2O = [glycogen-synthase I] + phosphate.","definition_xrefs":["EC:3.1.3.42","MetaCyc:GLYCOGEN-SYNTHASE-D-PHOSPHATASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoprotein phosphatase activity","termid":"GO:0004721"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004721"},{"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:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0016787","GO:0004721","GO:0003674","GO:0016788","GO:0003824"],"is_obsolete":false,"name":"[glycogen-synthase-D] phosphatase activity","synonyms":[{"name":"Mg2+ dependent glycogen synthase phosphatase activity","type":"related"},{"name":"UDP-glucose:glycogen 4-alpha-D-glucosyltransferase-D phosphohydrolase activity","type":"related"},{"name":"UDP-glycogen glucosyltransferase phosphatase activity","type":"related"},{"name":"UDPglucose-glycogen glucosyltransferase phosphatase activity","type":"related"},{"name":"UDPglucose:glycogen 4-alpha-D-glucosyltransferase-D phosphohydrolase activity","type":"related"},{"name":"glycogen glucosyltransferase phosphatase activity","type":"related"},{"name":"glycogen synthase D phosphatase activity","type":"related"},{"name":"glycogen synthase phosphatase activity","type":"related"},{"name":"glycogen synthetase phosphatase activity","type":"related"},{"name":"glycogen-synthase-D phosphatase activity","type":"related"},{"name":"phosphatase type 2oC","type":"related"},{"name":"uridine diphosphoglucose-glycogen glucosyltransferase phosphatase activity","type":"related"}],"termid":"GO:0050407"}


id: GO:0090453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of aspartate into the vacuole across the vacuolar membrane.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aspartate transmembrane transport","termid":"GO:0015810"},{"relation_name":"is_a","term_name":"vacuolar transmembrane transport","termid":"GO:0034486"},{"relation_name":"is_a","term_name":"vacuolar amino acid transmembrane transport","termid":"GO:0034487"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"aspartate transmembrane import into vacuole","synonyms":[{"name":"vacuolar aspartate import","type":"exact"}],"termid":"GO:0090453"}


id: MONDO:0004450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A occlusion precerebral artery that involves the carotid artery segment.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"occlusion precerebral artery","termid":"MONDO:0003718"},{"relation_name":"is_a","term_name":"carotid artery disorder","termid":"MONDO:0005269"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carotid artery occlusion","secondary_identifiers":["SCTID:266254007","ICD9:433.10","DOID:807","UMLS:C0265101","MEDGEN:539079"],"synonyms":[{"name":"carotid artery segment occlusion precerebral artery","type":"exact"},{"name":"occlusion and stenosis of carotid artery","type":"exact"},{"name":"occlusion precerebral artery of carotid artery segment","type":"exact"}],"termid":"MONDO:0004450","xrefs":{"Monarch":{"xref_id":"0004450"}}}


id: PR:O74387
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rav2 gene.","definition_xrefs":["UniProtKB:O74387","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":"regulator of V-ATPase in vacuolar membrane protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3H7.12","synonyms":[{"name":"RAVE complex subunit rav2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rav2","type":"exact"}],"termid":"PR:O74387"}


id: PBO:0088729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESCRT III complex subunit Did2","termid":"PBO:0088729"}


id: MONDO:0008850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cooper-Wang-Jabs syndrome is a multiple malformation syndrome characterized by atresia of the auditory canal together with ventricular septal defect, anteriorly displaced anus, mild clubfoot, and intellectual deficit. It has been described only once, in two sisters. The mode of inheritance is most likely autosomal recessive.","definition_xrefs":["Orphanet:1488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cooper-Jabs syndrome","secondary_identifiers":["OMIM:209770","GARD:16567","UMLS:C1859591","MEDGEN:347912","MESH:C565923","SCTID:720748007"],"synonyms":[{"name":"aural atresia, multiple congenital anomalies, and intellectual disability","type":"related"},{"name":"aural atresia, multiple congenital anomalies, and mental retardation","type":"related"},{"name":"aural atresia-multiple congenital anomalies-intellectual disability syndrome","type":"exact"}],"termid":"MONDO:0008850","xrefs":{"Monarch":{"xref_id":"0008850"}}}


id: MONDO:0044231
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete eyebrow, whorl 1n (obsolete MONDO:0044231)","secondary_identifiers":["OMIM:133800"],"synonyms":[{"name":"eyebrow, whorl in","type":"related"}],"termid":"MONDO:0044231","xrefs":{"Monarch":{"xref_id":"0044231"}}}


id: MONDO:1012415
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"sebaceous adenitis, non-human animal","termid":"MONDO:1011755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sebaceous adenitis, dog","secondary_identifiers":["OMIA:001563-9615"],"termid":"MONDO:1012415","xrefs":{"Monarch":{"xref_id":"1012415"}}}


id: SO:0000844
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of sequence which is a promoter for RNA polymerase II.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000844 RNApol_II_promoter_region (obsolete SO:0000844)","termid":"SO:0000844"}


id: GO:0015918
data:
  {"annotated_genes":["SJAG_01407","SJAG_02375","SJAG_00261","SJAG_03718","SJAG_01722","SJAG_02323","SJAG_00355","SJAG_01329","SJAG_01590"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94572,102933,108527,109688,111659,116551],"is_not":false,"summary":null,"term":"GO:0015918"},{"annotations":[106656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120011"},{"annotations":[62346,72312,77285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032366"}]},"cv_name":"biological_process","definition":"The directed movement of sterols into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Sterols are steroids with one or more hydroxyl groups and a hydrocarbon side-chain in the molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transport","termid":"GO:0006869"},{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00261":null,"SJAG_00355":null,"SJAG_01329":null,"SJAG_01407":null,"SJAG_01590":null,"SJAG_01722":null,"SJAG_02323":null,"SJAG_02375":null,"SJAG_03718":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"sterol transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0015918","terms_by_termid":{"GO:0015918":null,"GO:0032366":null,"GO:0120011":null}}


id: PBO:0068646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 27, pseudogene","termid":"PBO:0068646"}


id: PBO:0051392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda constant/OR22-2 (pseudogene)","termid":"PBO:0051392"}


id: PBO:0005843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein Pof7","termid":"PBO:0005843"}


id: GO:0140568
data:
  {"annotated_genes":["SJAG_01435","SJAG_04203"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140569"},{"annotations":[75044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140570"}]},"cv_name":"biological_process","definition":"The removal of a mislocalized protein from a cellular membrane.","definition_xrefs":["PMID:28712723","PMID:32973005","PMID:24821790"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of protein localization to membrane","termid":"GO:0090150"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01435":null,"SJAG_04203":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":"extraction of mislocalized protein from membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0140568","terms_by_termid":{"GO:0140569":null,"GO:0140570":null}}


id: MONDO:1010689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AA amyloidosis that occurs in Sumatran tiger.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AA amyloidosis, non-human animal","termid":"MONDO:1010092"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AA amyloidosis, Sumatran tiger","secondary_identifiers":["OMIA:000038-9695"],"termid":"MONDO:1010689","xrefs":{"Monarch":{"xref_id":"1010689"}}}


id: MONDO:0003834
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the cardia of stomach.","direct_ancestors":[{"relation_name":"is_a","term_name":"cardia cancer","termid":"MONDO:0001063"},{"relation_name":"is_a","term_name":"gastric carcinoma","termid":"MONDO:0004950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"gastric cardia carcinoma","secondary_identifiers":["NCIT:C6794","EFO:1001252","MEDGEN:234295","DOID:6270","UMLS:C1333763"],"synonyms":[{"name":"cancer of gastric cardia","type":"exact"},{"name":"cancer of the gastric cardia","type":"exact"},{"name":"carcinoma of cardia of stomach","type":"exact"},{"name":"carcinoma of gastric cardia","type":"exact"},{"name":"carcinoma of the cardia of the stomach","type":"exact"},{"name":"carcinoma of the gastric cardia","type":"exact"},{"name":"cardia of stomach carcinoma","type":"exact"},{"name":"gastric cardia (stomach) cancer","type":"exact"},{"name":"gastric cardia cancer","type":"exact"}],"termid":"MONDO:0003834","xrefs":{"Monarch":{"xref_id":"0003834"}}}


id: PBO:0079262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetratricopeptide repeat domain 33","termid":"PBO:0079262"}


id: PBO:0005566
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.6.1.11","termid":"PBO:0005566"}


id: PBO:0003911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mating-type m-specific polypeptide mc 2","termid":"PBO:0003911"}


id: PBO:0076789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tectorin alpha","termid":"PBO:0076789"}


id: PBO:0086008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; subunit of the leading edge protein (LEP) complex (Ssp1-Ady3-Don1-Irc10) that forms a ring-like structure at the leading edge of the prospore membrane during meiosis II; null mutant displays increased levels of spontaneous Rad52p foci","termid":"PBO:0086008"}


id: GO:0007193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway in which the signal is transmitted via the inhibition of adenylyl cyclase activity and a subsequent decrease in the intracellular concentration of cyclic AMP (cAMP).","definition_xrefs":["GOC:signaling","GOC:mah","ISBN:0815316194","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylate cyclase-modulating G protein-coupled receptor signaling pathway","termid":"GO:0007188"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway","secondary_identifiers":["Reactome:R-HSA-170670"],"synonyms":[{"name":"G protein signaling, adenylate cyclase inhibiting pathway","type":"exact"},{"name":"G protein signaling, adenylyl cyclase inhibiting pathway","type":"exact"},{"name":"G protein signalling, adenylate cyclase inhibiting pathway","type":"exact"},{"name":"G protein signalling, adenylyl cyclase inhibiting pathway","type":"exact"},{"name":"G-protein signaling, adenylate cyclase inhibiting pathway","type":"exact"},{"name":"G-protein signaling, adenylyl cyclase inhibiting pathway","type":"exact"},{"name":"G-protein signalling, adenylate cyclase inhibiting pathway","type":"exact"},{"name":"G-protein signalling, adenylyl cyclase inhibiting pathway","type":"exact"},{"name":"GPCR signaling pathway via inhibition of adenylate cyclase activity","type":"exact"},{"name":"adenylate cyclase-inhibiting GPCR signaling pathway","type":"exact"},{"name":"inhibition of adenylate cyclase activity by G-protein signaling pathway","type":"related"}],"termid":"GO:0007193"}


id: MOD:00638
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces two hydrogen atoms of an L-arginine residue with two (13)C,3x(2)H labeled methyl groups to form a 2x(13)C,6x(2)H labeled dimethylated L-arginine.","definition_xrefs":["Unimod:330","PubMed:15782174"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"dimethylated L-arginine","termid":"MOD:00783"},{"relation_name":"is_a","term_name":"(2)H deuterium labeled residue","termid":"MOD:00839"},{"relation_name":"is_a","term_name":"(13)C labeled residue","termid":"MOD:00842"},{"relation_name":"is_a","term_name":"modified L-arginine residue","termid":"MOD:00902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2x(13)C,6x(2)H labeled dimethylated L-arginine","synonyms":[{"name":"Dimethyl:2H(6)13C(2)","type":"related"},{"name":"dimethylated arginine","type":"related"}],"termid":"MOD:00638"}


id: PBO:0047520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FEZ family zinc finger 2","termid":"PBO:0047520"}


id: PBO:0063046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paralemmin 2","termid":"PBO:0063046"}


id: GO:0015855
data:
  {"annotated_genes":["SJAG_03970","SJAG_04717","SJAG_04714"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88411],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905530"},{"annotations":[88754],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904082"},{"annotations":[95860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098721"}]},"cv_name":"biological_process","definition":"The directed movement of pyrimidine nucleobases, one of the two classes of nitrogen-containing ring compounds found in DNA and RNA, 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":"nucleobase transport","termid":"GO:0015851"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03970":null,"SJAG_04714":null,"SJAG_04717":null},"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:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"pyrimidine nucleobase transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pyrimidine base transmembrane transport","type":"exact"},{"name":"pyrimidine base transport","type":"exact"},{"name":"pyrimidine transmembrane transport","type":"related"},{"name":"pyrimidine transport","type":"related"}],"termid":"GO:0015855","terms_by_termid":{"GO:0098721":null,"GO:1904082":null,"GO:1905530":null}}


id: PBO:0082864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Core Sm protein Sm D3; part of heteroheptameric complex (with Smb1p, Smd1p, Smd2p, Sme1p, Smx3p, and Smx2p) that is part of the spliceosomal U1, U2, U4, and U5 snRNPs; homolog of human Sm D3","termid":"PBO:0082864"}


id: PBO:0073535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain containing kinase binding protein 1","termid":"PBO:0073535"}


id: MONDO:0024288
data:
  {"annotated_genes":["SJAG_05213","SJAG_03785","SJAG_01344"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85630,85631,85632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009380"}]},"cv_name":"mondo","definition":"A disease characterized by elevated level of the pigment bilirubin in the blood.","direct_ancestors":[{"relation_name":"is_a","term_name":"bilirubin metabolism disease","termid":"MONDO:0024431"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01344":null,"SJAG_03785":null,"SJAG_05213":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hyperbilirubinemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0311468","MESH:D006932","MEDGEN:86321","SCTID:14783006"],"synonyms":[{"name":"bilirubinemia","type":"related"},{"name":"hyperbilirubinemia","type":"exact"}],"termid":"MONDO:0024288","terms_by_termid":{"MONDO:0009380":null},"xrefs":{"Monarch":{"xref_id":"0024288"}}}


id: MONDO:0004389
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infestations with arthropods of the subclass acari, superorder Acariformes.","definition_xrefs":["MESH:D008924"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic ectoparasitic infectious disease","termid":"MONDO:0002875"}],"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":"mite infestation","secondary_identifiers":["SCTID:240885009","DOID:7894","UMLS:C0026229","ICD9:133","ICD9:133.9","MEDGEN:7661"],"termid":"MONDO:0004389","xrefs":{"Monarch":{"xref_id":"0004389"}}}


id: GO:0106236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation/production of a glycolipid surfactant that acts as a bacterial biofilm dispersal.","definition_xrefs":["GOC:vw","PMID:28715477"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolipid biosynthetic process","termid":"GO:0009247"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"rhamnolipid biosynthesis","synonyms":[{"name":"rhamnolipid production","type":"related"}],"termid":"GO:0106236"}


id: PATO:0000993
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000993 relative viscosity (obsolete PATO:0000993)","termid":"PATO:0000993"}


id: PBO:0053257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipoic acid synthetase","termid":"PBO:0053257"}


id: FYPO:0000010
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell adhesion phenotype observed in the vegetative growth phase of the life cycle in which cells fail to adhere to a substrate.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell adhesion during vegetative growth","termid":"FYPO:0000009"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abolished cell-substrate adhesion","synonyms":[{"name":"abolished cell-substrate adhesion during mitotic cell cycle","type":"related"},{"name":"cell-substrate adhesion abolished","type":"exact"},{"name":"cell-substrate adhesion abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0000010"}


id: PR:Q9UTR1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An MMS19 nucleotide excision repair protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01599","PANTHER:PTHR12891:SF0","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/transcription protein mms19 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1071.02","secondary_identifiers":["UniProtKB:Q9UTR1"],"synonyms":[{"name":"Spom972h-MMS19","type":"exact"}],"termid":"PR:Q9UTR1"}


id: MONDO:0006032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the urinary bladder.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary bladder disorder","termid":"MONDO:0006026"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystitis","secondary_identifiers":["UMLS:C0010692","MESH:D003556","ICD9:595.89","MEDGEN:8227","NCIT:C26738","DOID:1679","ICD9:595","ICD9:595.9","SCTID:38822007","icd11.foundation:1181120673","EFO:1000025"],"synonyms":[{"name":"bladder infection","type":"exact"},{"name":"inflammation of urinary bladder","type":"exact"},{"name":"urinary bladder inflammation","type":"exact"}],"termid":"MONDO:0006032","xrefs":{"Monarch":{"xref_id":"0006032"}}}


id: PBO:0061005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NHS like 1","termid":"PBO:0061005"}


id: MONDO:0014863
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":"macrocephaly, dysmorphic facies, and psychomotor retardation","secondary_identifiers":["MEDGEN:934733","OMIM:617011","UMLS:C4310766"],"synonyms":[{"name":"MDFPMR","type":"exact"},{"name":"macrocephaly, dysmorphic facies, and psychomotor retardation","type":"exact"},{"name":"macrocephaly, dysmorphic facies, and psychomotor retardation; MDFPMR","type":"exact"}],"termid":"MONDO:0014863","xrefs":{"Monarch":{"xref_id":"0014863"}}}


id: GO:0050486
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a hydroxyl group from one position to another within a single molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"intramolecular hydroxytransferase activity","secondary_identifiers":["EC:5.4.4.-"],"synonyms":[{"name":"intramolecular transferase activity, transferring hydroxy groups","type":"exact"}],"termid":"GO:0050486"}


id: PATO:0001057
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001057 relative acceleration (obsolete PATO:0001057)","termid":"PATO:0001057"}


id: MONDO:0018217
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Koolen-de Vries syndrome","termid":"MONDO:0012496"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Koolen-de Vries syndrome due to a point mutation","secondary_identifiers":["GARD:21559","Orphanet:363965","UMLS:C5680974","MEDGEN:1843302"],"termid":"MONDO:0018217","xrefs":{"Monarch":{"xref_id":"0018217"}}}


id: MONDO:0043543
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any adverse condition in a patient occurring as the result of treatment by a physician, surgeon, or other health professional, especially infections acquired by a patient during the course of treatment.","definition_xrefs":["MESH:D007049"],"direct_ancestors":[{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iatrogenic disease","secondary_identifiers":["MEDGEN:9393","UMLS:C0020732","ICD9:799.9","SCTID:12456005","ICD10CM:T80-T88"],"synonyms":[{"name":"condition, hospital-acquired","type":"related"},{"name":"conditions, hospital-acquired","type":"related"},{"name":"disease, iatrogenic","type":"related"},{"name":"diseases, iatrogenic","type":"related"},{"name":"hospital acquired condition","type":"related"},{"name":"hospital-acquired condition","type":"related"},{"name":"hospital-acquired conditions","type":"related"},{"name":"iatrogenic diseases","type":"related"},{"name":"iatrogenic disorder","type":"exact"}],"termid":"MONDO:0043543","xrefs":{"Monarch":{"xref_id":"0043543"}}}


id: PBO:0004952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper amine oxidase-like protein Cao2","termid":"PBO:0004952"}


id: PBO:0053210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LGALS8 antisense RNA 1","termid":"PBO:0053210"}


id: PBO:0044671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"damage specific DNA binding protein 2","termid":"PBO:0044671"}


id: MONDO:0016240
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemimelia is a limb malformation characterized by the absence or gross shortening of the lower portion of one or more of the limbs. The condition is designated according to which bone of the distal arm or leg is absent or defective and includes fibular, radial, tibial, or ulnar hemimelia. Hemimelia ranges in severity.","definition_xrefs":["Orphanet:2130"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"non-syndromic limb reduction defect","termid":"MONDO:0019713"}],"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":"hemimelia","secondary_identifiers":["NCIT:C34674","MedDRA:10019464","GARD:18761","SCTID:33076008","MEDGEN:9194","UMLS:C0018987"],"synonyms":[{"name":"longitudinal meromelia","type":"exact"}],"termid":"MONDO:0016240","xrefs":{"Monarch":{"xref_id":"0016240"}}}


id: GO:0038004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process leading to the attainment of the full functional capacity of a ligand for an epidermal growth factor receptor. The ligand is functional when it can bind to and activate an epidermal growth factor receptor.","definition_xrefs":["PMID:11672524","PMID:11672525","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide hormone processing","termid":"GO:0016486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0051604","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"epidermal growth factor receptor ligand maturation","secondary_identifiers":["GO:0038005"],"synonyms":[{"name":"EGFR ligand maturation","type":"exact"},{"name":"EGFR ligand maturation by peptide bond cleavage","type":"narrow"},{"name":"EGFR ligand processing","type":"narrow"},{"name":"epidermal growth factor receptor ligand processing","type":"related"},{"name":"peptide bond cleavage involved in EGFR ligand maturation","type":"narrow"},{"name":"peptide bond cleavage involved in epidermal growth factor receptor ligand maturation","type":"related"}],"termid":"GO:0038004"}


id: PATO:0000815
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000815 absolute odor acuity value (obsolete PATO:0000815)","termid":"PATO:0000815"}


id: MONDO:0000751
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polyp that arises from the surface of the cervix.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervix disorder","termid":"MONDO:0002256"},{"relation_name":"is_a","term_name":"uterine polyp","termid":"MONDO:0004701"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical polyp","secondary_identifiers":["NCIT:C2939","MEDGEN:507540","SCTID:65576009","UMLS:C0007855","HP:0030159","DOID:0060325","ICD9:219"],"synonyms":[{"name":"adenomatous polyp of cervix","type":"exact"},{"name":"adenomatous polyp of the cervix","type":"exact"},{"name":"adenomatous polyp of the uterine cervix","type":"exact"},{"name":"adenomatous polyp of uterine cervix","type":"exact"},{"name":"cervical polyp","type":"exact"},{"name":"cervical polyp (disease)","type":"exact"},{"name":"cervix adenomatous polyp","type":"exact"},{"name":"cervix polyp","type":"exact"},{"name":"cervix uteri adenomatous polyp","type":"exact"},{"name":"cervix uteri polyp","type":"exact"},{"name":"polyp of cervix","type":"exact"},{"name":"polyp of cervix uteri","type":"exact"},{"name":"polyp of the cervix","type":"exact"},{"name":"polyp of the cervix uteri","type":"exact"},{"name":"polyp of the uterine cervix","type":"exact"},{"name":"polyp of uterine cervix","type":"exact"},{"name":"uterine cervix adenomatous polyp","type":"exact"},{"name":"uterine cervix polyp","type":"exact"}],"termid":"MONDO:0000751","xrefs":{"Monarch":{"xref_id":"0000751"}}}


id: PBO:0052627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 6A","termid":"PBO:0052627"}


id: PBO:0056415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane associated ring-CH-type finger 11","termid":"PBO:0056415"}


id: MONDO:0022675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cataract skeletal anomalies","termid":"MONDO:0022675","xrefs":{"Monarch":{"xref_id":"0022675"}}}


id: PBO:0048325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 36","termid":"PBO:0048325"}


id: MONDO:0006508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete infantile epileptic encephalopathy (obsolete MONDO:0006508)","termid":"MONDO:0006508","xrefs":{"Monarch":{"xref_id":"0006508"}}}


id: MOD:01803
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to a methylated threonine, such as O-methyl-L-threonine or L-threonine methyl ester.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methylated residue","termid":"MOD:00393"},{"relation_name":"is_a","term_name":"methylated threonine","termid":"MOD:01418"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"O-methylated threonine","synonyms":[{"name":"OMeThr","type":"exact"}],"termid":"MOD:01803"}


id: PBO:0058472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5580","termid":"PBO:0058472"}


id: FYPO:0001187
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a population reaches stationary phase at, and maintains, a lower cell density than wild type.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"decreased cell density in stationary phase","synonyms":[{"name":"reduced cell density in stationary phase","type":"exact"}],"termid":"FYPO:0001187"}


id: PATO:0000785
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000785 muscle function value (obsolete PATO:0000785)","termid":"PATO:0000785"}


id: GO:0198738
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that mediates the transfer of information from one cell to another, medaited by a wnt family protein ligand. This process includes wnt signal transduction in the receiving cell, release of wnt ligand from a secreting cell as well as any processes that actively facilitate wnt transport and presentation to receptor on the receiving cell.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete cell-cell signaling by wnt (obsolete GO:0198738)","termid":"GO:0198738"}


id: GO:0050071
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,2-diacyl-sn-glycero-3-phospho-(1'-sn-glycerol) + L-lysyl-tRNA(Lys) = 1,2-diacyl-sn-glycero-3-phospho-1'-(3'-O-L-lysyl)-sn-glycerol + tRNA(Lys).","definition_xrefs":["EC:2.3.2.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyltransferase activity","termid":"GO:0016755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"phosphatidylglycerol lysyltransferase activity","secondary_identifiers":["MetaCyc:LYSYLTRANSFERASE-RXN","RHEA:10668"],"synonyms":[{"name":"lysylphosphatidylglycerol synthase activity","type":"exact"},{"name":"lysyltransferase activity","type":"broad"}],"termid":"GO:0050071"}


id: MONDO:0011482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the DES gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative defects of desmin","termid":"MONDO:0016187"},{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"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":"dilated cardiomyopathy 1I","secondary_identifiers":["OMIM:604765","MESH:C565752","GARD:15372","MEDGEN:387998","UMLS:C1858154","DOID:0110431"],"synonyms":[{"name":"CMD1I","type":"exact"},{"name":"DES familial isolated dilated cardiomyopathy","type":"exact"},{"name":"cardiomyopathy, dilated, 1I","type":"related"},{"name":"cardiomyopathy, dilated, type 1I","type":"exact"},{"name":"dilated cardiomyopathy type 1I","type":"exact"},{"name":"familial isolated dilated cardiomyopathy caused by mutation in DES","type":"exact"}],"termid":"MONDO:0011482","xrefs":{"Monarch":{"xref_id":"0011482"}}}


id: MONDO:0013945
data:
  {"annotated_genes":["SJAG_00326"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87557],"is_not":false,"summary":null,"term":"MONDO:0013945"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"adult Refsum disease","termid":"MONDO:0009958"},{"relation_name":"excluded_subClassOf","term_name":"peroxisome biogenesis disorder","termid":"MONDO:0019234"},{"relation_name":"is_a","term_name":"Zellweger spectrum disorders","termid":"MONDO:0019609"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00326":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0019053","MONDO:0005066","MONDO:0006025","MONDO:0005559","MONDO:0005244"],"is_obsolete":false,"name":"peroxisome biogenesis disorder 9B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C2749346","GARD:15871","MEDGEN:440765","DOID:0081438","OMIM:614879"],"synonyms":[{"name":"PBD9B","type":"related"},{"name":"Refsum disease, adult, 2","type":"related"},{"name":"peroxisome biogenesis disorder 9B","type":"exact"},{"name":"peroxisome biogenesis disorder type 9B","type":"exact"},{"name":"peroxisome biogenesis disorder, PEX7-related, atypical","type":"related"},{"name":"peroxisome biogenesis disorder, complementation group 11","type":"related"},{"name":"peroxisome biogenesis disorder, complementation group R","type":"related"}],"termid":"MONDO:0013945","terms_by_termid":{"MONDO:0013945":null},"xrefs":{"Monarch":{"xref_id":"0013945"}}}


id: PR:O74519
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- naa50 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74519"],"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 N-acetyltransferase C663.13c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC663.13c","synonyms":[{"name":"Spom972h-naa50","type":"exact"}],"termid":"PR:O74519"}


id: MONDO:1012723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Junctional epidermolysis bullosa that occurs in dogs due to a mutation in the LAMA3 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"junctionalis epidermolysis bullosa, dog","termid":"MONDO:1011548"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"junctional epidermolysis bullosa, LAMA3-related, dog","secondary_identifiers":["OMIA:001677-9615"],"synonyms":[{"name":"epidermolysis bullosa, junctionalis, LAMA3-related, dog","type":"exact"}],"termid":"MONDO:1012723","xrefs":{"Monarch":{"xref_id":"1012723"}}}


id: GO:0014738
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of muscle hyperplasia.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle adaptation","termid":"GO:0043502"},{"relation_name":"regulates","term_name":"muscle hyperplasia","termid":"GO:0014900"}],"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 muscle hyperplasia","termid":"GO:0014738"}


id: PBO:0039152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AK3 pseudogene 7","termid":"PBO:0039152"}


id: GO:0140510
data:
  {"annotated_genes":["SJAG_00680","SJAG_01745","SJAG_03729","SJAG_01374","SJAG_04148","SJAG_04578","SJAG_03200","SJAG_04284","SJAG_01584"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[110750,91267,110784,116366,96442,90449,91655,116739],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140599"},{"annotations":[94159],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140511"}]},"cv_name":"cellular_component","definition":"A narrow constricted region of the nucleus that forms around the anaphase spindle during closed mitosis, and connects the main portions of the newly forming daughter nuclei.","definition_xrefs":["PMID:32848252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"nucleus","termid":"GO:0005634"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00680":null,"SJAG_01374":null,"SJAG_01584":null,"SJAG_01745":null,"SJAG_03200":null,"SJAG_03729":null,"SJAG_04148":null,"SJAG_04284":null,"SJAG_04578":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"mitotic nuclear bridge","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"nuclear bridge","type":"broad"}],"termid":"GO:0140510","terms_by_termid":{"GO:0140511":null,"GO:0140599":null}}


id: MONDO:0007582
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Cockayne syndrome B (obsolete MONDO:0007582)","termid":"MONDO:0007582","xrefs":{"Monarch":{"xref_id":"0007582"}}}


id: PBO:0000593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbohydrate kinase (predicted)","termid":"PBO:0000593"}


id: MONDO:0044766
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Marfan Syndrome 3 (obsolete MONDO:0044766)","secondary_identifiers":["GTR:AN0100577","GTR:AN0100578"],"synonyms":[{"name":"MFS 3","type":"related"},{"name":"Marfan syndrome type 3","type":"related"}],"termid":"MONDO:0044766","xrefs":{"Monarch":{"xref_id":"0044766"}}}


id: GO:1900640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of austinol biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"regulates","term_name":"austinol biosynthetic process","termid":"GO:1900560"}],"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 austinol biosynthetic process","synonyms":[{"name":"regulation of austinol anabolism","type":"exact"},{"name":"regulation of austinol biosynthesis","type":"exact"},{"name":"regulation of austinol formation","type":"exact"},{"name":"regulation of austinol synthesis","type":"exact"}],"termid":"GO:1900640"}


id: MONDO:0016912
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosome 14q deletion is a chromosome abnormality that occurs when there is a missing (deleted) copy of genetic material on the long arm (q) of chromosome 14.","definition_xrefs":["GARD:0003722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of the long arm of chromosome 14","secondary_identifiers":["Orphanet:262110","GARD:3722","UMLS:C2931697","MEDGEN:444119"],"synonyms":[{"name":"14q deletion","type":"related"},{"name":"14q monosomy","type":"related"},{"name":"chromosome 14q deletion","type":"related"},{"name":"deletion 14q","type":"related"},{"name":"monosomy 14q","type":"related"},{"name":"partial deletion of chromosome 14q","type":"exact"},{"name":"partial deletion of the long arm of chromosome type 14","type":"exact"},{"name":"partial monosomy 14q","type":"related"},{"name":"partial monosomy of chromosome 14q","type":"exact"},{"name":"partial monosomy of the long arm of chromosome 14","type":"exact"}],"termid":"MONDO:0016912","xrefs":{"Monarch":{"xref_id":"0016912"}}}


id: PBO:0054074
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 1424","termid":"PBO:0054074"}


id: FYPO:0004849
data:
  {"alleles_by_uniquename":{"SJAG_02621:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02621","name":"ago1delta","uniquename":"SJAG_02621:allele-1"},"SJAG_03118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03118","name":"leo1delta","uniquename":"SJAG_03118:allele-1"},"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119651,119652],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006989"}],"single_locus_phenotype":[{"annotations":[119644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006989"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a protein metabolic process is normal (i.e. indistinguishable from wild type). A protein metabolic process is a series of chemical reactions and pathways involving a specific protein.","definition_xrefs":["GO:0019538","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal metabolic process","termid":"FYPO:0002496"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02621":null,"SJAG_03118":null,"SJAG_03689":null},"genotype_count":3,"genotypes_by_uniquename":{"ago1delta__leo1delta":{"display_name":"ago1delta leo1delta","display_uniquename":"ago1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02621:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]},"dcr1delta":{"display_name":"dcr1delta","display_uniquename":"dcr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]}]},"dcr1delta__leo1delta":{"display_name":"dcr1delta leo1delta","display_uniquename":"dcr1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03118","SJAG_03689","SJAG_02621"],"name":"normal protein metabolic process","references_by_uniquename":{"PMID:35226668":null},"single_locus_annotated_genes":["SJAG_03689"],"single_locus_genotype_uniquenames":["dcr1delta"],"synonyms":[{"name":"normal cellular protein metabolic process","type":"exact"},{"name":"normal protein metabolism","type":"exact"}],"termid":"FYPO:0004849","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000162":null,"FYPO:0006989":null}}


id: PBO:0088454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane-associated serine-rich cell wall sensor Mtl1/Mtl3","termid":"PBO:0088454"}


id: FYPO:0003835
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which horsetail movement is normal (i.e. indistinguishable from wild type). 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":"normal transport","termid":"FYPO:0001071"},{"relation_name":"is_a","term_name":"normal nucleus positioning","termid":"FYPO:0001389"},{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal horsetail movement","synonyms":[{"name":"normal dynein-driven meiotic oscillatory nuclear movement","type":"exact"},{"name":"normal horsetail nuclear movement","type":"exact"}],"termid":"FYPO:0003835"}


id: PBO:0046511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate rich 5","termid":"PBO:0046511"}


id: GO:0034036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a purine ribonucleoside bisphosphate, a compound consisting of a purine base linked to a ribose sugar esterified with one phosphate group attached to each of two different hydroxyl groups on the sugar.","definition_xrefs":["GOC:pde","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoside bisphosphate biosynthetic process","termid":"GO:0034030"},{"relation_name":"is_a","term_name":"purine nucleoside bisphosphate biosynthetic process","termid":"GO:0034033"},{"relation_name":"is_a","term_name":"purine ribonucleoside bisphosphate metabolic process","termid":"GO:0034035"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"purine ribonucleoside bisphosphate biosynthetic process","synonyms":[{"name":"purine ribonucleoside bisphosphate anabolism","type":"exact"},{"name":"purine ribonucleoside bisphosphate biosynthesis","type":"exact"},{"name":"purine ribonucleoside bisphosphate formation","type":"exact"},{"name":"purine ribonucleoside bisphosphate synthesis","type":"exact"}],"termid":"GO:0034036"}


id: GO:0051554
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving flavonols, a member of a class of vascular pigments formed by consecutive oxidative processes from the flavonoid intermediates flavanones and dihydroflavonols. Flavonols are the most widespread of the flavonoids and have a wide array of physiological activities.","definition_xrefs":["PMID:11402179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavone metabolic process","termid":"GO:0051552"}],"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":"flavonol metabolic process","synonyms":[{"name":"flavonol metabolism","type":"exact"}],"termid":"GO:0051554"}


id: PBO:0072261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S21","termid":"PBO:0072261"}


id: PBO:0034620
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_Cutin-1","termid":"PBO:0034620"}


id: PBO:0059172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myelin protein zero like 3","termid":"PBO:0059172"}


id: PBO:0113470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of TORC2, a regulator of plasma membrane (PM) homeostasis; C-terminal PH domain binds to phosphoinositide-(4,5)-bisphosphate (PI(4,5)P2); binds directly to Ypk2p a Tor2p substrate and downstream TORC2 effector through a conserved central CRIM domain; acts with Tsc11p as a scaffold important for the integrity of the TORC2 complex; dispensable for PM localization of TORC2; role in regulating actin organization and growth control; orthologous to human MAPKAP1/SIN1","termid":"PBO:0113470"}


id: PBO:0049696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan and proteoglycan link protein 2","termid":"PBO:0049696"}


id: MONDO:0010953
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fanconi anemia caused by mutations of the FANCE gene. This is a protein coding gene. It is required for the nuclear accumulation of FANCC and provides a critical bridge between the FA complex and FANCD2.","definition_xrefs":["NCIT:C125709"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fanconi anemia","termid":"MONDO:0019391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005046","MONDO:0021190","MONDO:0005066","MONDO:0005570"],"is_obsolete":false,"name":"Fanconi anemia complementation group E","secondary_identifiers":["GARD:15324","DOID:0111084","MEDGEN:463628","OMIM:600901","UMLS:C3160739"],"synonyms":[{"name":"FACE","type":"exact"},{"name":"FANCE","type":"exact"},{"name":"FANCE Fanconi anaemia","type":"exact"},{"name":"FANCE Fanconi anemia","type":"exact"},{"name":"Fanconi Anemia, complementation group type E","type":"exact"},{"name":"Fanconi anaemia caused by mutation in FANCE","type":"exact"},{"name":"Fanconi anaemia complementation group type E","type":"exact"},{"name":"Fanconi anemia caused by mutation in FANCE","type":"exact"},{"name":"Fanconi anemia complementation group E","type":"exact"},{"name":"Fanconi anemia complementation group type E","type":"exact"},{"name":"Fanconi anemia, complementation group E","type":"related"},{"name":"face","type":"exact"}],"termid":"MONDO:0010953","xrefs":{"Monarch":{"xref_id":"0010953"}}}


id: MONDO:0013725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary nonpolyposis colon cancer in which the cause of the disease is a mutation in the MLH3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Lynch syndrome","termid":"MONDO:0005835"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"hereditary nonpolyposis colon cancer","termid":"MONDO:0018630"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335","MONDO:0000426"],"is_obsolete":false,"name":"colorectal cancer, hereditary nonpolyposis, type 7","secondary_identifiers":["MEDGEN:346893","UMLS:C1858380","GARD:15799","DOID:0070276","MESH:C565777","OMIM:614385"],"synonyms":[{"name":"HNPCC7","type":"related"},{"name":"MLH3 hereditary nonpolyposis colon cancer","type":"exact"},{"name":"colorectal cancer, hereditary nonpolyposis, type 7","type":"exact"},{"name":"hereditary nonpolyposis colon cancer caused by mutation in MLH3","type":"exact"}],"termid":"MONDO:0013725","xrefs":{"Monarch":{"xref_id":"0013725"}}}


id: PBO:0001998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"geranylgeranyltransferase I beta subunit Cwg2","termid":"PBO:0001998"}


id: GO:0050366
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: feruloyl-CoA + tyramine = CoA + N-feruloyltyramine.","definition_xrefs":["EC:2.3.1.110","MetaCyc:TYRAMINE-N-FERULOYLTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0003674","GO:0016746","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"tyramine N-feruloyltransferase activity","secondary_identifiers":["RHEA:19685"],"synonyms":[{"name":"feruloyl-CoA tyramine N-feruloyl-CoA transferase activity","type":"related"},{"name":"feruloyl-CoA:tyramine N-(hydroxycinnamoyl)transferase activity","type":"related"},{"name":"feruloyltyramine synthase activity","type":"related"},{"name":"tyramine N-feruloyl-CoA transferase activity","type":"related"},{"name":"tyramine feruloyltransferase activity","type":"related"}],"termid":"GO:0050366"}


id: PBO:0034541
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_iron-sulfur_cluster_binding","termid":"PBO:0034541"}


id: GO:0102327
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H2O + a 3-oxoacyl-CoA = H+ + coenzyme A + a 3-oxoacid.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-oxoacyl-CoA hydrolase activity (obsolete GO:0102327)","termid":"GO:0102327"}


id: PBO:0082693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the INO80 chromatiin remodeling complex; target of the Mec1p/Tel1p DNA damage signaling pathway; proposed to link chromatin remodeling to replication checkpoint responses","termid":"PBO:0082693"}


id: PR:O59673
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atp14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59673"],"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 H, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29A3.10c","synonyms":[{"name":"Spom972h-atp14","type":"exact"}],"termid":"PR:O59673"}


id: FYPO:0005711
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells contain fewer protein complexes consisting of cyclin B1 and cyclin-dependent kinase 1 (CDK1) than normal.","definition_xrefs":["PomBase:mah","PMID:8087848"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered level of macromolecular complex during vegetative growth","termid":"FYPO:0003684"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased cyclin B1-CDK1 complex level","synonyms":[{"name":"cyclin B1-CDK1 complexes present at decreased level","type":"exact"},{"name":"decreased cyclin B1-CDK1 complex level during mitotic cell cycle","type":"related"},{"name":"decreased cyclin B1-CDK1 complex level during vegetative growth","type":"exact"},{"name":"reduced cyclin B1-CDK1 complex level","type":"exact"}],"termid":"FYPO:0005711"}


id: PBO:0017847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human TMEM165 homolog, implicated in calcium transport","termid":"PBO:0017847"}


id: PBO:0027393
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_phospholipid:diacylglycerol_acyltransferase_activity","termid":"PBO:0027393"}


id: MONDO:0016262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant smooth muscle neoplasm, arising from the uterine corpus. It is characterized by a proliferation of neoplastic spindle cells.","definition_xrefs":["NCIT:C6340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mixed endometrial stromal and smooth muscle tumor","termid":"MONDO:0004526"},{"relation_name":"is_a","term_name":"leiomyosarcoma","termid":"MONDO:0005058"},{"relation_name":"is_a","term_name":"uterine corpus sarcoma","termid":"MONDO:0005210"}],"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":"leiomyosarcoma of the corpus uteri","secondary_identifiers":["GARD:20477","UMLS:C0280631","DOID:5289","EFO:1001974","NORD:1817","ONCOTREE:ULMS","SCTID:447389009","Orphanet:213625","MEDGEN:83679"],"synonyms":[{"name":"Uterine Leiomyosarcoma","type":"exact"},{"name":"body of uterus leiomyosarcoma","type":"exact"},{"name":"corpus uteri leiomyosarcoma","type":"exact"},{"name":"leiomyosarcoma - uterus","type":"exact"},{"name":"leiomyosarcoma of body of uterus","type":"exact"},{"name":"leiomyosarcoma of corpus uteri","type":"exact"},{"name":"leiomyosarcoma of the body of uterus","type":"exact"},{"name":"leiomyosarcoma of the corpus uteri","type":"exact"},{"name":"leiomyosarcoma of the uterine body","type":"exact"},{"name":"leiomyosarcoma of the uterine corpus","type":"exact"},{"name":"leiomyosarcoma of the uterus","type":"exact"},{"name":"leiomyosarcoma of uterine body","type":"exact"},{"name":"leiomyosarcoma of uterine corpus","type":"exact"},{"name":"leiomyosarcoma of uterus","type":"exact"},{"name":"uterine body leiomyosarcoma","type":"exact"},{"name":"uterine corpus leiomyosarcoma","type":"exact"},{"name":"uterine leiomyosarcoma","type":"related"},{"name":"uterus leiomyosarcoma","type":"related"}],"termid":"MONDO:0016262","xrefs":{"Monarch":{"xref_id":"0016262"}}}


id: GO:0045457
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of ecdysteroids, a group of polyhydroxylated ketosteroids which initiate post-embryonic development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid hormone secretion","termid":"GO:0035929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"ecdysteroid secretion","termid":"GO:0045457"}


id: PBO:0114286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mon1-Ccz1 GEF complex subunit Ccz1","termid":"PBO:0114286"}


id: PBO:0062659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 13 subfamily C member 9","termid":"PBO:0062659"}


id: MOD:00162
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to O5-glucosylgalactosyl-L-hydroxylysine.","definition_xrefs":["PubMed:4319110","Unimod:393","PubMed:4288358","PubMed:15149698","RESID:AA0153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5-hydroxy-L-lysine","termid":"MOD:00037"},{"relation_name":"is_a","term_name":"O-glycosylated residue","termid":"MOD:00396"},{"relation_name":"is_a","term_name":"galactosylated residue","termid":"MOD:00476"},{"relation_name":"is_a","term_name":"glucosylated","termid":"MOD:00726"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O5-glucosylgalactosyl-L-hydroxylysine","synonyms":[{"name":"(2S,5R)-2,6-diamino-5-[2-O-(alpha-D-glucopyranosyl)-beta-D-galactopyranosyloxy]hexanoic acid","type":"exact"},{"name":"5-(2-O-alpha-D-glucopyranosyl-beta-D-galactopyranosyl)oxy-L-lysine","type":"exact"},{"name":"Glucosylgalactosyl","type":"related"},{"name":"O5-glucosylgalactosyl-L-hydroxylysine","type":"exact"},{"name":"OGlcGal5HyLys","type":"exact"},{"name":"glucosylgalactosyl hydroxylysine","type":"related"}],"termid":"MOD:00162"}


id: PBO:0054409
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 1805","termid":"PBO:0054409"}


id: PBO:0003606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial lipoic acid synthetase Lip5 (predicted)","termid":"PBO:0003606"}


id: FYECO:0000390
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which torin1 was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ torin1","synonyms":[{"name":"Torin1","type":"exact"}],"termid":"FYECO:0000390"}


id: MONDO:0700273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary cancer predisposition due to variation(s) in the RAD51C gene. Pathogenic germline variation in RAD51C confers an autosomal dominant predisposition to tumor formation at multiple primary sites, including ovarian cancer, triple negative breast cancer and ER negative breast cancer.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD51C-related cancer predisposition","termid":"MONDO:0700273","xrefs":{"Monarch":{"xref_id":"0700273"}}}


id: GO:0005818
data:
  {"annotated_genes":["SJAG_00655","SJAG_04387","SJAG_02336","SJAG_02286","SJAG_01613","SJAG_02509","SJAG_01297","SJAG_02045","SJAG_01370","SJAG_02695","SJAG_04003"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104326,107529,99526,107738,112456],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000235"},{"annotations":[91311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032117"},{"annotations":[88069],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990574"},{"annotations":[108568,79224,91701],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061673"},{"annotations":[97295],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905721"}]},"cv_name":"cellular_component","definition":"An array of microtubules emanating from a spindle pole MTOC that do not connect to kinetochores.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"},{"relation_name":"is_a","term_name":"supramolecular complex","termid":"GO:0099080"},{"relation_name":"part_of","term_name":"spindle","termid":"GO:0005819"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00655":null,"SJAG_01297":null,"SJAG_01370":null,"SJAG_01613":null,"SJAG_02045":null,"SJAG_02286":null,"SJAG_02336":null,"SJAG_02509":null,"SJAG_02695":null,"SJAG_04003":null,"SJAG_04387":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005575","GO:0015630"],"is_obsolete":false,"name":"aster","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0005818","terms_by_termid":{"GO:0000235":null,"GO:0032117":null,"GO:0061673":null,"GO:1905721":null,"GO:1990574":null}}


id: GO:0015541
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of cyanate from one side of a membrane to the other.","definition_xrefs":["TC:2.A.1.17.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyanate transmembrane transporter activity","termid":"GO:0015110"},{"relation_name":"is_a","term_name":"secondary active transmembrane transporter activity","termid":"GO:0015291"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"secondary active cyanate transmembrane transporter activity","synonyms":[{"name":"cyanate porter activity","type":"related"}],"termid":"GO:0015541"}


id: GO:0015531
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: citrate(out) + H+(out) = citrate(in) + H+(in).","definition_xrefs":["TC:2.A.1.6.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"},{"relation_name":"is_a","term_name":"citrate secondary active transmembrane transporter activity","termid":"GO:0071913"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"citrate:proton symporter activity","secondary_identifiers":["RHEA:32123"],"synonyms":[{"name":"citrate:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015531"}


id: PBO:0052412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1","termid":"PBO:0052412"}


id: PBO:0054408
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 1804","termid":"PBO:0054408"}


id: GO:0015232
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of heme from one side of a membrane to the other.","definition_xrefs":["PMID:29549126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"heme transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-9661408","Reactome:R-HSA-917870","Reactome:R-HSA-917892"],"synonyms":[{"name":"haem transporter activity","type":"exact"},{"name":"heme transporter activity","type":"broad"}],"termid":"GO:0015232"}


id: PBO:0029136
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_cordycepin","termid":"PBO:0029136"}


id: GO:0023066
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a signal is conveyed via the vascular system.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signal transmission via vascular system (obsolete GO:0023066)","synonyms":[{"name":"signal transmission via vascular system","type":"exact"}],"termid":"GO:0023066"}


id: MONDO:0001389
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coronary artery disorder","termid":"MONDO:0005010"},{"relation_name":"is_a","term_name":"congenital heart disease","termid":"MONDO:0005453"}],"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":"congenital coronary artery anomaly","secondary_identifiers":["MEDGEN:510602","DOID:11843","ICD9:746.85","SCTID:28574005","UMLS:C0158623"],"synonyms":[{"name":"congenital anomaly of coronary artery","type":"exact"},{"name":"coronary arteries congenital malformation","type":"exact"},{"name":"coronary artery abnormality","type":"exact"},{"name":"coronary artery abnormality [ambiguous]","type":"exact"},{"name":"coronary artery anomaly","type":"exact"},{"name":"coronary artery anomaly, congenital","type":"exact"}],"termid":"MONDO:0001389","xrefs":{"Monarch":{"xref_id":"0001389"}}}


id: PBO:0057694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1283-2","termid":"PBO:0057694"}


id: GO:1905001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of membrane repolarization during atrial cardiac muscle cell action potential.","definition_xrefs":["GOC:BHF","GOC:BHF_miRNA","GOC:rph","PMID:21098446","GOC:TermGenie","GO_REF:0000058","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane repolarization during atrial cardiac muscle cell action potential","termid":"GO:1905000"},{"relation_name":"is_a","term_name":"negative regulation of membrane repolarization during cardiac muscle cell action potential","termid":"GO:1905032"},{"relation_name":"negatively_regulates","term_name":"membrane repolarization during atrial cardiac muscle cell action potential","termid":"GO:0098914"}],"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 membrane repolarization during atrial cardiac muscle cell action potential","synonyms":[{"name":"down regulation of atrial repolarization","type":"related"},{"name":"down regulation of electrocardiogram QRS complex","type":"related"},{"name":"down regulation of membrane repolarization during atrial cardiac muscle cell action potential","type":"exact"},{"name":"down-regulation of atrial repolarization","type":"related"},{"name":"down-regulation of electrocardiogram QRS complex","type":"related"},{"name":"down-regulation of membrane repolarization during atrial cardiac muscle cell action potential","type":"exact"},{"name":"downregulation of atrial repolarization","type":"related"},{"name":"downregulation of electrocardiogram QRS complex","type":"related"},{"name":"downregulation of membrane repolarization during atrial cardiac muscle cell action potential","type":"exact"},{"name":"inhibition of atrial repolarization","type":"related"},{"name":"inhibition of electrocardiogram QRS complex","type":"related"},{"name":"inhibition of membrane repolarization during atrial cardiac muscle cell action potential","type":"narrow"},{"name":"negative regulation of atrial repolarization","type":"related"},{"name":"negative regulation of electrocardiogram QRS complex","type":"related"}],"termid":"GO:1905001"}


id: MONDO:0006697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Chlamydophila infectious disease (obsolete MONDO:0006697)","termid":"MONDO:0006697","xrefs":{"Monarch":{"xref_id":"0006697"}}}


id: PBO:0061406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptide S receptor 1","termid":"PBO:0061406"}


id: PBO:0027626
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_transcriptional_response_to_pheromone","termid":"PBO:0027626"}


id: SO:0000965
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Structural unit composed of a self-replicating, double-stranded RNA molecule.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"double","termid":"SO:0000985"},{"relation_name":"is_a","term_name":"RNA_chromosome","termid":"SO:0000961"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double_stranded_RNA_chromosome","synonyms":[{"name":"double stranded RNA chromosome","type":"exact"}],"termid":"SO:0000965"}


id: FYPO:0004028
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 5' deoxyribonuclease (pyrimidine dimer) activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal endodeoxyribonuclease activity","termid":"FYPO:0002036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0005447","FYPO:0000652","FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000002"],"is_obsolete":false,"name":"abnormal 5' deoxyribonuclease (pyrimidine dimer) activity","termid":"FYPO:0004028"}


id: PBO:0053385
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 312","termid":"PBO:0053385"}


id: GO:0043940
data:
  {"annotated_genes":["SJAG_04140","SJAG_02169","SJAG_04853","SJAG_00993"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[102610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[91052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[92511],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the formation of cellular spores derived from the products of meiosis.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sexual sporulation","termid":"GO:0034306"},{"relation_name":"is_a","term_name":"regulation of sporulation resulting in formation of a cellular spore","termid":"GO:0042173"},{"relation_name":"regulates","term_name":"sexual sporulation resulting in formation of a cellular spore","termid":"GO:0043935"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00993":null,"SJAG_02169":null,"SJAG_04140":null,"SJAG_04853":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of sexual sporulation resulting in formation of a cellular spore","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0043940","terms_by_termid":{"GO:0034307":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


id: MONDO:0043287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Obstruction of the blood flow in the superior vena cava caused by a malignant neoplasm, thrombosis, or aneurysm. It is a medical emergency requiring immediate treatment. Signs and symptoms include swelling and cyanosis of the face, neck, and upper arms, cough, orthopnea, and headache.","definition_xrefs":["NCIT:C3396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"superior vena cava syndrome","secondary_identifiers":["MEDGEN:52576","SCTID:63363004","MESH:D013479","UMLS:C0038833"],"synonyms":[{"name":"SVC obstruction","type":"related"},{"name":"SVC syndrome","type":"related"},{"name":"SVCS","type":"related"},{"name":"superior vena cava obstruction","type":"related"},{"name":"superior vena cava syndrome","type":"exact"},{"name":"superior vena cava thrombosis","type":"related"}],"termid":"MONDO:0043287","xrefs":{"Monarch":{"xref_id":"0043287"}}}


id: PBO:0013125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U1 snRNP-associated protein Luc7","termid":"PBO:0013125"}


id: PBO:0073167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SECIS binding protein 2 like","termid":"PBO:0073167"}


id: PBO:0050518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox D3","termid":"PBO:0050518"}


id: PBO:0058233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4522","termid":"PBO:0058233"}


id: GO:0060696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of phospholipid catabolism, the chemical reactions and pathways resulting in the breakdown of phospholipids, any lipid containing phosphoric acid as a mono- or diester.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lipid catabolic process","termid":"GO:0050994"},{"relation_name":"is_a","term_name":"regulation of phospholipid metabolic process","termid":"GO:1903725"},{"relation_name":"regulates","term_name":"phospholipid catabolic process","termid":"GO:0009395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"regulation of phospholipid catabolic process","termid":"GO:0060696"}


id: GO:0045930
data:
  {"annotated_genes":["SJAG_03501","SJAG_00318","SJAG_01680","SJAG_04682","SJAG_04597","SJAG_01605","SJAG_01708","SJAG_03681","SJAG_01082","SJAG_01146","SJAG_02404","SJAG_03353","SJAG_00600","SJAG_01330","SJAG_00991","SJAG_04671","SJAG_00327","SJAG_02563","SJAG_02392","SJAG_04813","SJAG_01837","SJAG_01068","SJAG_01401","SJAG_03942","SJAG_04280","SJAG_01677","SJAG_04126","SJAG_02332","SJAG_03591","SJAG_03529","SJAG_04943","SJAG_02026","SJAG_03898","SJAG_00996","SJAG_02576","SJAG_02162","SJAG_03067","SJAG_02098","SJAG_03695","SJAG_04394","SJAG_04259","SJAG_01855","SJAG_00169","SJAG_00457","SJAG_01118","SJAG_02169","SJAG_04699","SJAG_01210","SJAG_00145","SJAG_03854","SJAG_00429","SJAG_01873","SJAG_01956","SJAG_03126","SJAG_02074","SJAG_02336","SJAG_00364","SJAG_02592","SJAG_04884","SJAG_03073","SJAG_03486","SJAG_04332","SJAG_02723","SJAG_05288","SJAG_03720","SJAG_02266","SJAG_00883","SJAG_04999","SJAG_00082","SJAG_00623","SJAG_03048","SJAG_03026","SJAG_02771","SJAG_00071","SJAG_04140","SJAG_02451","SJAG_01076","SJAG_04287","SJAG_01084","SJAG_01679","SJAG_05373","SJAG_03371","SJAG_01044","SJAG_03602","SJAG_00640","SJAG_01311","SJAG_01205","SJAG_01429","SJAG_03927","SJAG_05346","SJAG_06592","SJAG_03160","SJAG_01297","SJAG_02858","SJAG_00526","SJAG_01010","SJAG_00486"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95481,90668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051728"},{"annotations":[116229,99912,104210,112292,114598,108574,91047,107552,114112],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[100862,94731,90319,116333,101758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044878"},{"annotations":[116561,78328,111527,114797,80328,116334,93890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044773"},{"annotations":[72775,116389,112367,117132,99679,117433,117605,106943,79141,109641,75084,100863,91754,99512,71459,79799,94286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033314"},{"annotations":[89266,101940,102678,109214,116231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031568"},{"annotations":[109994,91631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[98750,94863,96172,116335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031569"},{"annotations":[75578,117347,112059,90536,72773,109642,101373,99681,92117,100864,106944,91755,118040,79741,89443],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007095"},{"annotations":[74235,79514,79746,99682,79139,106945,116391,90771,112368,74758,91756,96333,112060,102679,107984,89444,89489,94864,101183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031573"},{"annotations":[114829,106646,99754,102117,110232,115886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[104759,118697,102682,106299,106974,109591,106137],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0110045"},{"annotations":[102685,68273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001100"},{"annotations":[92482,92063,93655,99197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000134"},{"annotations":[94691,107337,108895,112149,78808,101318,104818,93251,112810,111764,114798,93544,106975,93891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010972"},{"annotations":[117178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903464"},{"annotations":[98096,109218,102688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903467"},{"annotations":[94523],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[116813,118563],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140648"},{"annotations":[117005],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[101943,105241,94867,109369],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0110044"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of progression through the mitotic cell cycle.","definition_xrefs":["GOC:go_curators","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle","termid":"GO:0007346"},{"relation_name":"is_a","term_name":"negative regulation of cell cycle","termid":"GO:0045786"},{"relation_name":"negatively_regulates","term_name":"mitotic cell cycle","termid":"GO:0000278"}],"gene_count":97,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00082":null,"SJAG_00145":null,"SJAG_00169":null,"SJAG_00318":null,"SJAG_00327":null,"SJAG_00364":null,"SJAG_00429":null,"SJAG_00457":null,"SJAG_00486":null,"SJAG_00526":null,"SJAG_00600":null,"SJAG_00623":null,"SJAG_00640":null,"SJAG_00883":null,"SJAG_00991":null,"SJAG_00996":null,"SJAG_01010":null,"SJAG_01044":null,"SJAG_01068":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01118":null,"SJAG_01146":null,"SJAG_01205":null,"SJAG_01210":null,"SJAG_01297":null,"SJAG_01311":null,"SJAG_01330":null,"SJAG_01401":null,"SJAG_01429":null,"SJAG_01605":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01708":null,"SJAG_01837":null,"SJAG_01855":null,"SJAG_01873":null,"SJAG_01956":null,"SJAG_02026":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02162":null,"SJAG_02169":null,"SJAG_02266":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02392":null,"SJAG_02404":null,"SJAG_02451":null,"SJAG_02563":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02723":null,"SJAG_02771":null,"SJAG_02858":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03067":null,"SJAG_03073":null,"SJAG_03126":null,"SJAG_03160":null,"SJAG_03353":null,"SJAG_03371":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03529":null,"SJAG_03591":null,"SJAG_03602":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03720":null,"SJAG_03854":null,"SJAG_03898":null,"SJAG_03927":null,"SJAG_03942":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04332":null,"SJAG_04394":null,"SJAG_04597":null,"SJAG_04671":null,"SJAG_04682":null,"SJAG_04699":null,"SJAG_04813":null,"SJAG_04884":null,"SJAG_04943":null,"SJAG_04999":null,"SJAG_05288":null,"SJAG_05346":null,"SJAG_05373":null,"SJAG_06592":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mitotic cell cycle","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-8854050"],"synonyms":[{"name":"down regulation of progression through mitotic cell cycle","type":"exact"},{"name":"down-regulation of progression through mitotic cell cycle","type":"exact"},{"name":"downregulation of progression through mitotic cell cycle","type":"exact"},{"name":"inhibition of progression through mitotic cell cycle","type":"narrow"},{"name":"negative regulation of mitotic cell cycle progression","type":"exact"},{"name":"negative regulation of progression through mitotic cell cycle","type":"exact"}],"termid":"GO:0045930","terms_by_termid":{"GO:0001100":null,"GO:0007094":null,"GO:0007095":null,"GO:0010972":null,"GO:0031568":null,"GO:0031569":null,"GO:0031571":null,"GO:0031573":null,"GO:0033314":null,"GO:0044773":null,"GO:0044878":null,"GO:0051728":null,"GO:0090267":null,"GO:0110044":null,"GO:0110045":null,"GO:0140499":null,"GO:0140648":null,"GO:1902426":null,"GO:1903464":null,"GO:1903467":null,"GO:2000134":null}}


id: SO:0002022
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A small RNA molecule, 22-23 nt in size, that is the product of a longer RNA. The production of priRNAs is independent of dicer and involves binding of RNA by argonaute and trimming by triman. In fission yeast, priRNAs trigger the establishment of heterochromatin. PriRNAs are primarily generated from centromeric transcripts (dg and dh repeats), but may also be produced from degradation products of primary transcripts.","definition_xrefs":["PomBase:al","PMID:24095277","PMID:20178743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ncRNA","termid":"SO:0000655"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"priRNA","synonyms":[{"name":"primal small RNA","type":"exact"}],"termid":"SO:0002022"}


id: GO:0052823
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2Z,4E,7E)-2-hydroxy-6-oxonona-2,4,7-trienedioate + H2O = (2Z)-2-hydroxypenta-2,4-dienoate + fumarate + H+.","definition_xrefs":["RHEA:34191"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances","termid":"GO:0016823"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-hydroxy-6-oxonona-2,4,7-trienedioate hydrolase activity","secondary_identifiers":["MetaCyc:RXN-12070","KEGG_REACTION:R06789","UM-BBD_reactionID:r1622"],"synonyms":[{"name":"(2E,4Z,7E)-2-hydroxy-6-oxonona-2,4,7-trienedioate fumarylhydrolase activity","type":"exact"},{"name":"2-hydroxy-6-ketonona-2,4,7-trienedoic acid hydrolase activity","type":"exact"}],"termid":"GO:0052823"}


id: GO:0060855
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of venous endothelial cells out of the veins giving rise to the precursors of lymphatic endothelial cells.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel endothelial cell migration","termid":"GO:0043534"},{"relation_name":"part_of","term_name":"lymph vessel development","termid":"GO:0001945"}],"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":"venous endothelial cell migration involved in lymph vessel development","termid":"GO:0060855"}


id: PR:O13795
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pof8 gene.","definition_xrefs":["UniProtKB:O13795","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":"protein pof8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.17","synonyms":[{"name":"Spom972h-pof8","type":"exact"}],"termid":"PR:O13795"}


id: GO:0045959
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of complement activation by the classical pathway.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of humoral immune response mediated by circulating immunoglobulin","termid":"GO:0002924"},{"relation_name":"is_a","term_name":"regulation of complement activation, classical pathway","termid":"GO:0030450"},{"relation_name":"is_a","term_name":"negative regulation of complement activation","termid":"GO:0045916"},{"relation_name":"negatively_regulates","term_name":"complement activation, classical pathway","termid":"GO:0006958"}],"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 complement activation, classical pathway","synonyms":[{"name":"down regulation of complement activation, classical pathway","type":"exact"},{"name":"down-regulation of complement activation, classical pathway","type":"exact"},{"name":"downregulation of complement activation, classical pathway","type":"exact"},{"name":"inhibition of complement activation, classical pathway","type":"narrow"},{"name":"negative regulation of complement cascade, classical pathway","type":"exact"}],"termid":"GO:0045959"}


id: GO:1902391
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of N-terminal peptidyl-serine acetylation.","definition_xrefs":["PMID:23912279","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of N-terminal peptidyl-serine acetylation (obsolete GO:1902391)","synonyms":[{"name":"activation of N-terminal peptidyl-serine acetylation","type":"narrow"},{"name":"up regulation of N-terminal peptidyl-serine acetylation","type":"exact"},{"name":"up-regulation of N-terminal peptidyl-serine acetylation","type":"exact"},{"name":"upregulation of N-terminal peptidyl-serine acetylation","type":"exact"}],"termid":"GO:1902391"}


id: PBO:0080428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS51 pseudogene 12","termid":"PBO:0080428"}


id: MONDO:0014470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the TBC1D24 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 65","secondary_identifiers":["MEDGEN:856147","OMIM:616044","UMLS:C3892048","DOID:0110586","GARD:18140"],"synonyms":[{"name":"DFNA65","type":"narrow"},{"name":"TBC1D24 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"autosomal dominant deafness 65","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 65","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in TBC1D24","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 65","type":"narrow"},{"name":"deafness, autosomal dominant 65","type":"narrow"},{"name":"deafness, autosomal dominant type 65","type":"narrow"}],"termid":"MONDO:0014470","xrefs":{"Monarch":{"xref_id":"0014470"}}}


id: PBO:0050360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 63","termid":"PBO:0050360"}


id: GO:1905571
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that binds interleukin-10 (IL-10) and that consists of, at a minimum, a dimeric interleukin, an alpha and a beta chain as well as optional additional kinase subunits. The alpha chain binds IL-10 with high affinity and subsequently binds the common beta receptor chain that forms part of multiple interleukin receptors.","definition_xrefs":["PMID:16982608","GOC:TermGenie","GO_REF:0000088","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor complex","termid":"GO:0043235"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"interleukin-10 receptor complex","synonyms":[{"name":"IL-10 receptor complex","type":"exact"},{"name":"IL-10-receptor complex","type":"exact"},{"name":"IL10 receptor complex","type":"exact"},{"name":"interleukin-10-receptor complex","type":"exact"}],"termid":"GO:1905571"}


id: GO:0018564
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9H-carbazole + H+ + NAD(P)H + O2 = 2'-aminobiphenyl-2,3-diol + NAD(P)+.","definition_xrefs":["EC:1.14.12.22"],"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 two atoms of oxygen into one donor","termid":"GO:0016708"}],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"carbazole 1,9a-dioxygenase [NAD(P)H] activity","secondary_identifiers":["UM-BBD_reactionID:r0456"],"synonyms":[{"name":"CARDO","type":"exact"},{"name":"carbazole 1,9alpha-dioxygenase activity","type":"exact"}],"termid":"GO:0018564"}


id: MONDO:0011716
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute hemorrhagic leukoencephalitis(AHL) is a veryrareform of acute disseminated encephalomyelitis that usuallyresults indeath. It is characterized by a brief but intense attack of inflammation in the brain and spinal cord that damages the myelin -- the protective covering of the nerve fibers. It may also cause bleeding in the brain, leading to damage of the white matter. Symptoms usually come on quickly, beginning with symptoms such as fever, neck stiffness, fatigue, headache, nausea vomiting,seizures, and coma.AHL has a very poor prognosis, with rapid deterioration and death usually occurring within days to one week after onset of symptoms because of severe inflammation in the brain. Although the exact cause is unclear,AHL usually followsaviral infection, or less often, vaccination for measles, mumps, or rubella. Some researchers think that an infection or vaccination can initiate an autoimmune process in the body thus leading to AHL.","direct_ancestors":[{"relation_name":"is_a","term_name":"acute hemorrhagic encephalitis","termid":"MONDO:0003337"},{"relation_name":"is_a","term_name":"acute disseminated encephalomyelitis","termid":"MONDO:0019383"}],"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":"acute hemorrhagic leukoencephalitis","secondary_identifiers":["DOID:10992","MEDGEN:4937","NCIT:C84535","OMIM:606752","SCTID:72986009","UMLS:C0014077","EFO:0007132","ICD9:136.9","MESH:D004684","GARD:8629"],"synonyms":[{"name":"AHL","type":"exact"},{"name":"AHLE","type":"related"},{"name":"Ahl","type":"related"},{"name":"Weston-Hurst syndrome","type":"exact"},{"name":"acute haemorrhagic leucoencephalitis of Weston Hurst","type":"exact"},{"name":"acute hemorrhagic encephalomyelitis","type":"exact"},{"name":"acute hemorrhagic leukoencephalitis","type":"exact"},{"name":"acute necrotizing hemorrhagic leukoencephalitis","type":"exact"}],"termid":"MONDO:0011716","xrefs":{"Monarch":{"xref_id":"0011716"}}}


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


id: MONDO:0013838
data:
  {"annotated_genes":["SJAG_01865"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86625],"is_not":false,"summary":null,"term":"MONDO:0013838"}]},"cv_name":"mondo","definition":"Any coenzyme Q10 deficiency in which the cause of the disease is a mutation in the PDSS2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coenzyme Q10 deficiency","termid":"MONDO:0018151"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01865":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005244","MONDO:0004069"],"is_obsolete":false,"name":"coenzyme Q10 deficiency, primary, 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3553358","MEDGEN:766272","DOID:0070240","GARD:18379","OMIM:614652"],"synonyms":[{"name":"COQ10D3","type":"related"},{"name":"PDSS2 coenzyme Q10 deficiency","type":"exact"},{"name":"coenzyme Q10 deficiency caused by mutation in PDSS2","type":"exact"},{"name":"coenzyme Q10 deficiency, primary, 3","type":"exact"},{"name":"coenzyme Q10 deficiency, primary, type 3","type":"exact"}],"termid":"MONDO:0013838","terms_by_termid":{"MONDO:0013838":null},"xrefs":{"Monarch":{"xref_id":"0013838"}}}


id: PBO:0109258
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 A opposite strand","termid":"PBO:0109258"}


id: PBO:0031258
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_cell_cycle_DNA_replication_checkpoint","termid":"PBO:0031258"}


id: PBO:0054749
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 2159","termid":"PBO:0054749"}


id: PBO:0003687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfate adenylyltransferase","termid":"PBO:0003687"}


id: GO:1990528
data:
  {"annotated_genes":["SJAG_00185","SJAG_00700"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72390,74302],"is_not":false,"summary":null,"term":"GO:1990528"}]},"cv_name":"cellular_component","definition":"A protein complex that is involved in endocytosis in the yeast S. cerevisiae.","definition_xrefs":["PMID:20610658","GOC:rb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00185":null,"SJAG_00700":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:0005575","GO:0032991"],"is_obsolete":false,"name":"Rvs161p-Rvs167p complex","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:1990528","terms_by_termid":{"GO:1990528":null}}


id: SO:0001722
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 36th residue (a lysine), from the start of the H3 histone protein is mono-methylated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"H3K36_methylation_site","termid":"SO:0001733"}],"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":"H3K36_monomethylation_site","synonyms":[{"name":"H3K36 mono-methylation site","type":"exact"},{"name":"H3K36Me1","type":"related"}],"termid":"SO:0001722"}


id: MONDO:0002350
data:
  {"annotated_genes":["SJAG_01374","SJAG_03986","SJAG_04017","SJAG_00864","SJAG_04013","SJAG_04148","SJAG_03361","SJAG_00933","SJAG_00093","SJAG_04621","SJAG_00471","SJAG_01185","SJAG_04000","SJAG_03182"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[85423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011303"},{"annotations":[86228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014752"},{"annotations":[86153,86152],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014817"},{"annotations":[86151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014818"},{"annotations":[86712],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032580"},{"annotations":[86714,86713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032581"},{"annotations":[86710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032582"},{"annotations":[86238,86237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026726"},{"annotations":[85340],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014099"},{"annotations":[86157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014257"}]},"cv_name":"mondo","definition":"An instance of nephrotic syndrome that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephrotic syndrome","termid":"MONDO:0005377"},{"relation_name":"is_a","term_name":"inherited kidney disorder","termid":"MONDO:0100191"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00093":null,"SJAG_00471":null,"SJAG_00864":null,"SJAG_00933":null,"SJAG_01185":null,"SJAG_01374":null,"SJAG_03182":null,"SJAG_03361":null,"SJAG_03986":null,"SJAG_04000":null,"SJAG_04013":null,"SJAG_04017":null,"SJAG_04148":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"familial nephrotic syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:502251","NCIT:C35337","icd11.foundation:1524476844","OMIMPS:256300","SCTID:48796009","UMLS:C3501848","DOID:2590"],"synonyms":[{"name":"congenital nephrotic syndrome","type":"exact"},{"name":"hereditary nephrotic syndrome","type":"exact"}],"termid":"MONDO:0002350","terms_by_termid":{"MONDO:0011303":null,"MONDO:0013836":null,"MONDO:0014099":null,"MONDO:0014257":null,"MONDO:0014752":null,"MONDO:0014817":null,"MONDO:0014818":null,"MONDO:0026726":null,"MONDO:0032580":null,"MONDO:0032581":null,"MONDO:0032582":null},"xrefs":{"Monarch":{"xref_id":"0002350"}}}


id: GO:0036436
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An Isw1 complex that binds DNA and has nucleosome-stimulated ATPase activity. In S. cerevisiae, contains an Isw1p ATPase subunit in complex with Ioc3p.","definition_xrefs":["PMID:12482963","GOC:jd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Isw1 complex","termid":"GO:0016587"}],"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":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005694","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"Isw1a complex","termid":"GO:0036436"}


id: GO:0010482
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the physical partitioning and separation of an epidermal cell into daughter cells. An epidermal cell is any of the cells that make up the epidermis.","definition_xrefs":["PMID:17450124"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell division","termid":"GO:0051302"},{"relation_name":"regulates","term_name":"epidermal cell division","termid":"GO:0010481"}],"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 epidermal cell division","synonyms":[{"name":"regulation of hypodermal cell division","type":"related"}],"termid":"GO:0010482"}


id: PBO:0025541
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae VAM7","termid":"PBO:0025541"}


id: PBO:0074051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 31","termid":"PBO:0074051"}


id: MONDO:0019743
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete nephropathy secondary to a storage or other metabolic disease (obsolete MONDO:0019743)","secondary_identifiers":["Orphanet:93593"],"termid":"MONDO:0019743","xrefs":{"Monarch":{"xref_id":"0019743"}}}


id: MONDO:0032566
data:
  {"annotated_genes":["SJAG_02719"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86699],"is_not":false,"summary":null,"term":"MONDO:0032566"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02719":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"squalene synthase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618156","MEDGEN:1648421","UMLS:C4748427"],"synonyms":[{"name":"SQSD","type":"related"},{"name":"SQUALENE SYNTHASE DEFICIENCY","type":"related"},{"name":"neurodevelopmental disorder with low cholesterol and abnormal urine organic acids","type":"related"}],"termid":"MONDO:0032566","terms_by_termid":{"MONDO:0032566":null},"xrefs":{"Monarch":{"xref_id":"0032566"}}}


id: PR:O60138
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- wbp4 gene.","definition_xrefs":["UniProtKB:O60138","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C18H10.07 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18H10.07","synonyms":[{"name":"Spom972h-wbp4","type":"exact"}],"termid":"PR:O60138"}


id: GO:1904170
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of bleb assembly.","definition_xrefs":["GOC:TermGenie","GOC:als","GO_REF:0000058","PMID:25651887"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of plasma membrane bounded cell projection assembly","termid":"GO:0120032"},{"relation_name":"regulates","term_name":"bleb assembly","termid":"GO:0032060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"regulation of bleb assembly","synonyms":[{"name":"regulation of cell blebbing","type":"exact"}],"termid":"GO:1904170"}


id: PBO:0011063
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in fungi only","termid":"PBO:0011063"}


id: PBO:0045038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dispatched RND transporter family member 3","termid":"PBO:0045038"}


id: PBO:0048351
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 62","termid":"PBO:0048351"}


id: GO:0046086
data:
  {"annotated_genes":["SJAG_01070","SJAG_00044"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89204],"is_not":false,"summary":null,"term":"GO:0046086"},{"annotations":[117167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006169"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of adenosine, adenine riboside, a ribonucleoside found widely distributed in cells of every type as the free nucleoside and in combination in nucleic acids and various nucleoside coenzymes.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenosine metabolic process","termid":"GO:0046085"},{"relation_name":"is_a","term_name":"purine ribonucleoside biosynthetic process","termid":"GO:0046129"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_01070":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"adenosine biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"adenosine anabolism","type":"exact"},{"name":"adenosine biosynthesis","type":"exact"},{"name":"adenosine formation","type":"exact"},{"name":"adenosine synthesis","type":"exact"}],"termid":"GO:0046086","terms_by_termid":{"GO:0006169":null,"GO:0046086":null}}


id: PBO:0082641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of inositol phosphorylceramide (IPC) synthase; forms a complex with Aur1p and regulates its activity; required for IPC synthase complex localization to the Golgi; post-translationally processed by Kex2p; KEI1 is an essential gene","termid":"PBO:0082641"}


id: PBO:0085621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in efficient MVB sorting of proteins to the vacuole; may function as an RSP5 adapter protein for MVB cargos; integral membrane protein localized to vacuolar intralumenal vesicles","termid":"PBO:0085621"}


id: PBO:0034700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cohesin loading factor (adherin) Mis4","termid":"PBO:0034700"}


id: MONDO:0021569
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Emery-Dreifuss muscular dystrophy inherited in an autosomal dominant pattern and caused by mutations in the LMNA gene.","definition_xrefs":["NCIT:C126745"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy, limb-girdle, autosomal dominant","termid":"MONDO:0015151"},{"relation_name":"is_a","term_name":"autosomal dominant Emery-Dreifuss muscular dystrophy","termid":"MONDO:0020336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005267","MONDO:0005336"],"is_obsolete":false,"name":"Emery-Dreifuss muscular dystrophy 2, autosomal dominant","secondary_identifiers":["DOID:0070247","SCTID:718178006","GARD:10230","Orphanet:264","SCTID:240072005","MEDGEN:98048","OMIM:181350","MESH:C535898","OMIM:159001","DOID:0110301","ICD9:425.4","UMLS:C0410190"],"synonyms":[{"name":"EDMD2","type":"exact"},{"name":"EMD2","type":"related"},{"name":"Emery-Dreifuss muscular dystrophy 2, autosomal dominant","type":"exact"},{"name":"Emery-Dreifuss muscular dystrophy, autosomal dominant","type":"related"},{"name":"Hauptmann-Thannhauser muscular dystrophy","type":"exact"},{"name":"LGMD1B","type":"exact"},{"name":"LMNA autosomal dominant limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal dominant limb-girdle muscular dystrophy caused by mutation in LMNA","type":"exact"},{"name":"autosomal dominant limb-girdle muscular dystrophy type 1B","type":"exact"},{"name":"benign scapuloperoneal muscular dystrophy with cardiomyopathy","type":"related"},{"name":"limb-girdle muscular dystrophy due to lamin A/C deficiency","type":"exact"},{"name":"limb-girdle muscular dystrophy type 1B","type":"related"},{"name":"muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant","type":"related"},{"name":"muscular dystrophy, limb-girdle type 1B","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 1B","type":"related"},{"name":"muscular dystrophy, proximal, type 1B","type":"related"},{"name":"proximal muscular dystrophy type 1B","type":"exact"},{"name":"scapuloilioperoneal atrophy with cardiopathy","type":"related"}],"termid":"MONDO:0021569","xrefs":{"Monarch":{"xref_id":"0021569"}}}


id: MONDO:0013354
data:
  {"annotated_genes":["SJAG_00797"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87382],"is_not":false,"summary":null,"term":"MONDO:0013354"}]},"cv_name":"mondo","definition":"Any autosomal recessive spastic ataxia in which the cause of the disease is a mutation in the MTPAP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"autosomal recessive spastic ataxia","termid":"MONDO:0017847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00797":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"spastic ataxia 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:10992","MEDGEN:462275","OMIM:613672","Orphanet:254343","ICD10CM:G11.4","UMLS:C3150925","DOID:0050943"],"synonyms":[{"name":"MTPAP autosomal recessive spastic ataxia","type":"exact"},{"name":"SPAX4","type":"exact"},{"name":"autosomal recessive spastic ataxia - optic atrophy - dysarthria","type":"related"},{"name":"autosomal recessive spastic ataxia 4","type":"related"},{"name":"autosomal recessive spastic ataxia caused by mutation in MTPAP","type":"exact"},{"name":"autosomal recessive spastic ataxia type 4","type":"exact"},{"name":"autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome","type":"related"},{"name":"spastic ataxia 4, autosomal recessive","type":"related"},{"name":"spastic ataxia type 4","type":"exact"}],"termid":"MONDO:0013354","terms_by_termid":{"MONDO:0013354":null},"xrefs":{"Monarch":{"xref_id":"0013354"}}}


id: PBO:0059502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded ATP synthase membrane subunit 6","termid":"PBO:0059502"}


id: PBO:0048681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgi glycoprotein 1","termid":"PBO:0048681"}


id: MONDO:0031006
data:
  {"annotated_genes":["SJAG_01671"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85902],"is_not":false,"summary":null,"term":"MONDO:0031006"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01671":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"neurodegeneration with ataxia and late-onset optic atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5543254","MEDGEN:1779901","OMIM:619259"],"synonyms":[{"name":"NDAXOA","type":"exact"}],"termid":"MONDO:0031006","terms_by_termid":{"MONDO:0031006":null},"xrefs":{"Monarch":{"xref_id":"0031006"}}}


id: GO:0044195
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Long, dynamic tubular channels, formed by invagination of the nuclear envelope, that extend deep into the nucleoplasm. The channels have an underlying lamina and are implicated in functioning in signaling and transport.","definition_xrefs":["PMID:17959832","PMID:9024685","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"nuclear envelope","termid":"GO:0005635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"nucleoplasmic reticulum","synonyms":[{"name":"nuclear channels","type":"exact"}],"termid":"GO:0044195"}


id: GO:0018666
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,4-dichlorophenol + NADPH + H+ + O2 = 3,5-dichlorocatechol + NADP+ + H2O.","definition_xrefs":["EC:1.14.13.20"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"2,4-dichlorophenol 6-monooxygenase activity","secondary_identifiers":["UM-BBD_enzymeID:r0275","RHEA:20920","MetaCyc:24-DICHLOROPHENOL-6-MONOOXYGENASE-RXN"],"synonyms":[{"name":"2,4-dichlorophenol hydroxylase activity","type":"exact"},{"name":"2,4-dichlorophenol monooxygenase activity","type":"related"},{"name":"2,4-dichlorophenol,NADPH:oxygen oxidoreductase (6-hydroxylating)","type":"related"}],"termid":"GO:0018666"}


id: PBO:0079300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha tocopherol transfer protein like","termid":"PBO:0079300"}


id: PBO:0051125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 1/OR16-3 (pseudogene)","termid":"PBO:0051125"}


id: MONDO:1010978
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Huntington disease that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Huntington disease, non-human animal","termid":"MONDO:1010231"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Huntington disease, sheep","secondary_identifiers":["OMIA:000485-9940"],"termid":"MONDO:1010978","xrefs":{"Monarch":{"xref_id":"1010978"}}}


id: PBO:0026878
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-binucleate_multiseptate_cell,_septa_grouped","termid":"PBO:0026878"}


id: GO:0003711
data:
  {"annotated_genes":["SJAG_02393","SJAG_03481","SJAG_00483","SJAG_00540","SJAG_02691","SJAG_02238","SJAG_04353","SJAG_02097","SJAG_03211","SJAG_01707"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72694,92300,92973,94274,100258,105834,107151,108210,113517,118266],"is_not":false,"summary":null,"term":"GO:0003711"}]},"cv_name":"molecular_function","definition":"A molecular function that stimulates the elongation properties of the RNA polymerase during the elongation phase of transcription. A subclass of transcription elongation factors enable the transition from transcription initiation to elongation, while another class rescue stalled RNA polymerases.","definition_xrefs":["GOC:txnOH-2018","PMID:23878398","PMID:28892040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription regulator activity","termid":"GO:0140110"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00483":null,"SJAG_00540":null,"SJAG_01707":null,"SJAG_02097":null,"SJAG_02238":null,"SJAG_02393":null,"SJAG_02691":null,"SJAG_03211":null,"SJAG_03481":null,"SJAG_04353":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140110"}],"interesting_parent_ids":["GO:0140110","GO:0003674"],"is_obsolete":false,"name":"transcription elongation factor activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"transcription elongation regulator activity","type":"related"},{"name":"transcriptional elongation regulator activity","type":"related"}],"termid":"GO:0003711","terms_by_termid":{"GO:0003711":null}}


id: PBO:0087217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-AdoMet-dependent methyltransferase involved in lipid homeostasis; mediates resistance to a drug cantharidin","termid":"PBO:0087217"}


id: PBO:0049128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPRC5D and HEBP1 antisense RNA 1","termid":"PBO:0049128"}


id: PBO:0057971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3689d-1","termid":"PBO:0057971"}


id: FYPO:0002189
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 viable, is shaped in the form of a spheroid, and has a normal volume.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal volume spheroid vegetative cell","termid":"FYPO:0000946"},{"relation_name":"is_a","term_name":"viable vegetative cell, abnormal cell shape, normal cell size","termid":"FYPO:0001510"},{"relation_name":"is_a","term_name":"viable spheroid vegetative cell","termid":"FYPO:0002380"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000257"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000005","FYPO:0001312","FYPO:0000004","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"viable normal volume spheroid vegetative cell","synonyms":[{"name":"viable normal volume rounded vegetative cell","type":"exact"},{"name":"viable normal volume spheroid cell during vegetative growth","type":"exact"},{"name":"viable normal volume spheroid vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002189"}


id: PBO:0003933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxidised protein hydrolase (predicted)","termid":"PBO:0003933"}


id: GO:1904326
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of circadian sleep/wake cycle, wakefulness.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:10923657"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of circadian sleep/wake cycle, wakefulness","termid":"GO:0010840"},{"relation_name":"is_a","term_name":"negative regulation of circadian rhythm","termid":"GO:0042754"},{"relation_name":"is_a","term_name":"negative regulation of behavior","termid":"GO:0048521"},{"relation_name":"negatively_regulates","term_name":"circadian sleep/wake cycle, wakefulness","termid":"GO:0042746"}],"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 circadian sleep/wake cycle, wakefulness","synonyms":[{"name":"down regulation of circadian sleep/wake cycle, wakefulness","type":"exact"},{"name":"down-regulation of circadian sleep/wake cycle, wakefulness","type":"exact"},{"name":"downregulation of circadian sleep/wake cycle, wakefulness","type":"exact"},{"name":"inhibition of circadian sleep/wake cycle, wakefulness","type":"narrow"}],"termid":"GO:1904326"}


id: PR:Q11119
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ubiquitin carboxyl-terminal hydrolase 5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["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":"ubiquitin carboxyl-terminal hydrolase 14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC6B1.06c","secondary_identifiers":["UniProtKB:Q11119"],"synonyms":[{"name":"SPBC6B1.06c","type":"related"},{"name":"Spom972h-USP5","type":"exact"},{"name":"UBA domain-containing protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"deubiquitinating enzyme 14 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin thioesterase 14 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-specific-processing protease 14 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ucp2","type":"related"}],"termid":"PR:Q11119"}


id: GO:0018084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of N-terminal peptidyl-serine to lactic acid.","definition_xrefs":["RESID:AA0186"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-lactic acid biosynthetic process from peptidyl-serine (obsolete GO:0018084)","synonyms":[{"name":"peptidyl-lactic acid anabolism from peptidyl-serine","type":"exact"},{"name":"peptidyl-lactic acid formation from peptidyl-serine","type":"exact"},{"name":"peptidyl-lactic acid synthesis from peptidyl-serine","type":"exact"}],"termid":"GO:0018084"}


id: PBO:0028356
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_phosphatase_activity","termid":"PBO:0028356"}


id: PBO:0036403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein modifier, ubiquitin","termid":"PBO:0036403"}


id: GO:0047669
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sucrose + 1,4-alpha-D-glucosyl(n) = D-fructose + 1,4-alpha-D-glucosyl(n+1).","definition_xrefs":["EC:2.4.1.4","MetaCyc:AMYLOSUCRASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016757"],"is_obsolete":false,"name":"amylosucrase activity","secondary_identifiers":["RHEA:24572"],"synonyms":[{"name":"sucrose-1,4-alpha-glucan glucosyltransferase activity","type":"related"},{"name":"sucrose-glucan glucosyltransferase activity","type":"related"},{"name":"sucrose:1,4-alpha-D-glucan 4-alpha-D-glucosyltransferase activity","type":"related"}],"termid":"GO:0047669"}


id: FYPO:0002658
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 trehalose 6-phosphate measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular trehalose 6-phosphate level","synonyms":[{"name":"increased cellular trehalose 6-phosphate level during mitotic cell cycle","type":"related"},{"name":"increased cellular trehalose 6-phosphate level during vegetative growth","type":"exact"},{"name":"increased cellular trehalose-6P level","type":"exact"},{"name":"increased trehalose 6-phosphate accumulation","type":"related"}],"termid":"FYPO:0002658"}


id: GO:2000860
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of aldosterone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mineralocorticoid secretion","termid":"GO:2000857"},{"relation_name":"is_a","term_name":"regulation of aldosterone secretion","termid":"GO:2000858"},{"relation_name":"positively_regulates","term_name":"aldosterone secretion","termid":"GO:0035932"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"positive regulation of aldosterone secretion","termid":"GO:2000860"}


id: PBO:0074061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC25A38 pseudogene 1","termid":"PBO:0074061"}


id: GO:1900106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hyaluranon cable assembly.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component biogenesis","termid":"GO:0044089"},{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of hyaluranon cable assembly","termid":"GO:1900104"},{"relation_name":"positively_regulates","term_name":"hyaluranon cable assembly","termid":"GO:0036118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of hyaluranon cable assembly","synonyms":[{"name":"activation of HA cable assembly","type":"exact"},{"name":"activation of hyaluranon cable assembly","type":"narrow"},{"name":"positive regulation of HA cable assembly","type":"exact"},{"name":"up regulation of HA cable assembly","type":"exact"},{"name":"up regulation of hyaluranon cable assembly","type":"exact"},{"name":"up-regulation of HA cable assembly","type":"exact"},{"name":"up-regulation of hyaluranon cable assembly","type":"exact"},{"name":"upregulation of HA cable assembly","type":"exact"},{"name":"upregulation of hyaluranon cable assembly","type":"exact"}],"termid":"GO:1900106"}


id: PR:P27584
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gpa1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P27584"],"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":"guanine nucleotide-binding protein alpha-1 subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC24C6.06","synonyms":[{"name":"GP1-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gpa1","type":"exact"}],"termid":"PR:P27584"}


id: FYPO:0006112
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 dimethylation of lysine at position 9 of histone H3 in silent mating-type cassettes does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished histone H3-K9 dimethylation at centromere during vegetative growth","termid":"FYPO:0004170"},{"relation_name":"is_a","term_name":"abnormal histone methylation at silent mating-type cassette during vegetative growth","termid":"FYPO:0007373"},{"relation_name":"is_a","term_name":"abolished histone H3-K9 methylation at silent mating-type cassette during vegetative growth","termid":"FYPO:0008212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0002274","FYPO:0000002","FYPO:0002494"],"is_obsolete":false,"name":"abolished histone H3-K9 dimethylation at silent mating-type cassette during vegetative growth","synonyms":[{"name":"abolished histone H3 K9 dimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"abolished histone H3-K9 dimethylation at mating-type region heterochromatin during vegetative growth","type":"exact"},{"name":"abolished histone H3-K9 dimethylation at silent mating-type cassette during mitotic cell cycle","type":"related"},{"name":"abolished histone H3K9me2 at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"abolished histone lysine H3 K9 dimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"abolished silent mating-type cassette histone H3-K9 dimethylation during vegetative growth","type":"exact"},{"name":"histone H3-K9 dimethylation abolished at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"histone H3-K9 dimethylation absent at silent mating-type cassette during vegetative growth","type":"exact"}],"termid":"FYPO:0006112"}


id: GO:0032868
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 an insulin stimulus. Insulin is a polypeptide hormone produced by the islets of Langerhans of the pancreas in mammals, and by the homologous organs of other organisms.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to peptide hormone","termid":"GO:0043434"}],"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 insulin","synonyms":[{"name":"response to insulin stimulus","type":"exact"}],"termid":"GO:0032868"}


id: PBO:0111348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small subunit processome, U3 snoRNP-associated WD repeat protein Utp4","termid":"PBO:0111348"}


id: GO:1905569
data:
  {"annotated_genes":["SJAG_00792"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94381],"is_not":false,"summary":null,"term":"GO:1905569"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ferrichrome biosynthetic process.","definition_xrefs":["GOC:al","GOC:TermGenie","PMID:654321","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of amide metabolic process","termid":"GO:0034249"},{"relation_name":"is_a","term_name":"negative regulation of siderophore biosynthetic process","termid":"GO:1900705"},{"relation_name":"is_a","term_name":"regulation of ferrichrome biosynthetic process","termid":"GO:1905568"},{"relation_name":"negatively_regulates","term_name":"ferrichrome biosynthetic process","termid":"GO:0031169"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00792":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"negative regulation of ferrichrome biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of ferrichrome anabolism","type":"exact"},{"name":"down regulation of ferrichrome biosynthesis","type":"exact"},{"name":"down regulation of ferrichrome biosynthetic process","type":"exact"},{"name":"down regulation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"down regulation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"down regulation of ferrichrome formation","type":"exact"},{"name":"down regulation of ferrichrome synthesis","type":"exact"},{"name":"down-regulation of ferrichrome anabolism","type":"exact"},{"name":"down-regulation of ferrichrome biosynthesis","type":"exact"},{"name":"down-regulation of ferrichrome biosynthetic process","type":"exact"},{"name":"down-regulation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"down-regulation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"down-regulation of ferrichrome formation","type":"exact"},{"name":"down-regulation of ferrichrome synthesis","type":"exact"},{"name":"downregulation of ferrichrome anabolism","type":"exact"},{"name":"downregulation of ferrichrome biosynthesis","type":"exact"},{"name":"downregulation of ferrichrome biosynthetic process","type":"exact"},{"name":"downregulation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"downregulation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"downregulation of ferrichrome formation","type":"exact"},{"name":"downregulation of ferrichrome synthesis","type":"exact"},{"name":"inhibition of ferrichrome anabolism","type":"narrow"},{"name":"inhibition of ferrichrome biosynthesis","type":"narrow"},{"name":"inhibition of ferrichrome biosynthetic process","type":"narrow"},{"name":"inhibition of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"inhibition of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"inhibition of ferrichrome formation","type":"narrow"},{"name":"inhibition of ferrichrome synthesis","type":"narrow"},{"name":"negative regulation of ferrichrome anabolism","type":"exact"},{"name":"negative regulation of ferrichrome biosynthesis","type":"exact"},{"name":"negative regulation of ferrichrome biosynthetic process, peptide formation","type":"narrow"},{"name":"negative regulation of ferrichrome biosynthetic process, peptide modification","type":"narrow"},{"name":"negative regulation of ferrichrome formation","type":"exact"},{"name":"negative regulation of ferrichrome synthesis","type":"exact"}],"termid":"GO:1905569","terms_by_termid":{"GO:1905569":null}}


id: GO:1902952
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of dendritic spine maintenance.","definition_xrefs":["GOC:TermGenie","PMID:24328732","GO_REF:0000058","GOC:sjp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell projection organization","termid":"GO:0031346"},{"relation_name":"is_a","term_name":"regulation of dendritic spine maintenance","termid":"GO:1902950"},{"relation_name":"positively_regulates","term_name":"dendritic spine maintenance","termid":"GO:0097062"}],"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 dendritic spine maintenance","synonyms":[{"name":"activation of dendritic spine maintenance","type":"narrow"},{"name":"up regulation of dendritic spine maintenance","type":"exact"},{"name":"up-regulation of dendritic spine maintenance","type":"exact"},{"name":"upregulation of dendritic spine maintenance","type":"exact"}],"termid":"GO:1902952"}


id: PBO:0075795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfiredoxin 1","termid":"PBO:0075795"}


id: GO:0031627
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which linear telomeric DNA is remodeled into duplex loops, by the invasion of a 3' single-stranded overhang into the duplex region.","definition_xrefs":["GOC:vw","PMID:10338214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomere maintenance","termid":"GO:0000723"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0032200"}],"interesting_parent_ids":["GO:0006259","GO:0032200","GO:0008150"],"is_obsolete":false,"name":"telomeric loop formation","synonyms":[{"name":"T loop biosynthesis","type":"exact"},{"name":"T loop formation","type":"exact"},{"name":"t-loop biosynthesis","type":"exact"},{"name":"t-loop formation","type":"exact"}],"termid":"GO:0031627"}


id: FYPO:0005033
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the phosphorylation of one or more specific proteins, or of specific protein sites, is abnormal when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein phosphorylation","termid":"FYPO:0002677"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0000002","FYPO:0005447","FYPO:0002274","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein phosphorylation during nitrogen starvation","synonyms":[{"name":"abnormal protein phosphorylation during cellular response to nitrogen starvation","type":"exact"},{"name":"abnormal protein phosphorylation during nitrogen depletion","type":"exact"},{"name":"abnormal protein phosphorylation during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0005033"}


id: GO:0000309
data:
  {"annotated_genes":["SJAG_02889","SJAG_01500"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71023,75079],"is_not":false,"summary":null,"term":"GO:0000309"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-nicotinamide D-ribonucleotide + ATP + H+ = diphosphate + NAD+.","definition_xrefs":["RHEA:21360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylyltransferase activity","termid":"GO:0070566"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01500":null,"SJAG_02889":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016779"],"is_obsolete":false,"name":"nicotinamide-nucleotide adenylyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:2.7.7.1-RXN","Reactome:R-HSA-8939959","EC:2.7.7.1"],"synonyms":[{"name":"ATP:NMN adenylyltransferase activity","type":"related"},{"name":"ATP:nicotinamide-nucleotide adenylyltransferase activity","type":"exact"},{"name":"NAD(+) diphosphorylase activity","type":"narrow"},{"name":"NAD(+) pyrophosphorylase activity","type":"narrow"},{"name":"NAD+ diphosphorylase activity","type":"related"},{"name":"NAD+ pyrophosphorylase activity","type":"related"},{"name":"NMN adenylyltransferase activity","type":"narrow"},{"name":"NMNAT activity","type":"narrow"},{"name":"adenosine triphosphate-nicotinamide mononucleotide transadenylase activity","type":"related"},{"name":"diphosphopyridine nucleotide pyrophosphorylase activity","type":"related"},{"name":"nicotinamide adenine dinucleotide pyrophosphorylase activity","type":"narrow"},{"name":"nicotinamide mononucleotide adenylyltransferase activity","type":"narrow"}],"termid":"GO:0000309","terms_by_termid":{"GO:0000309":null}}


id: MONDO:0018704
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete actinomycosis (obsolete MONDO:0018704)","termid":"MONDO:0018704","xrefs":{"Monarch":{"xref_id":"0018704"}}}


id: PBO:0087742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the SWI/SNF chromatin remodeling complex; involved in transcriptional regulation; functions interdependently in transcriptional activation with Snf2p and Snf6p; relocates to the cytosol under hypoxic conditions","termid":"PBO:0087742"}


id: GO:0075131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont activates, maintains or increases the frequency, rate or extent of protein kinase-mediated signal transduction in 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 induction by symbiont of host protein kinase-mediated signal transduction (obsolete GO:0075131)","termid":"GO:0075131"}


id: GO:0032941
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of a substance by a tissue.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"is_a","term_name":"secretion","termid":"GO:0046903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"secretion by tissue","synonyms":[{"name":"expulsion of gland contents","type":"related"},{"name":"tissue secretion","type":"exact"}],"termid":"GO:0032941"}


id: PBO:0038763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin related protein 3C","termid":"PBO:0038763"}


id: GO:0050286
data:
  {"annotated_genes":["SJAG_04964"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100591],"is_not":false,"summary":null,"term":"GO:0050286"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucitol 6-phosphate + H2O = D-glucitol + phosphate.","definition_xrefs":["RHEA:24580","EC:3.1.3.50"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04964":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"sorbitol-6-phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R02866","MetaCyc:SORBITOL-6-PHOSPHATASE-RXN"],"synonyms":[{"name":"sorbitol-6-phosphate phosphatase activity","type":"related"},{"name":"sorbitol-6-phosphate phosphohydrolase activity","type":"related"}],"termid":"GO:0050286","terms_by_termid":{"GO:0050286":null}}


id: PBO:0035951
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_intracellular_protein_transport_during_vegetative_growth","termid":"PBO:0035951"}


id: MONDO:0020554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Heiner syndrome, also called cow's milk hypersensitivity, is a food induced pulmonary hypersensiting syndrome that affects primarily infants and that is characterized by pulmonary hemosiderosis, digestive bleeding, anemia and poor growing, improving with elimination of cow's milk from the diet.","definition_xrefs":["Orphanet:99932"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary pulmonary hemosiderosis","termid":"MONDO:0020553"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Heiner syndrome","secondary_identifiers":["UMLS:C3873343","GARD:19714","ICD10EXP:J99.8*","SCTID:707441009","MEDGEN:844833","icd11.foundation:187112249","ICD10EXP:E83.1+","ICD9:518.89"],"synonyms":[{"name":"cow's milk hypersensitivity","type":"exact"}],"termid":"MONDO:0020554","xrefs":{"Monarch":{"xref_id":"0020554"}}}


id: PBO:0055997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LSM1 homolog, mRNA degradation associated","termid":"PBO:0055997"}


id: GO:0032296
data:
  {"annotated_genes":["SJAG_03689","SJAG_04019","SJAG_02156","SJAG_04527","SJAG_01463","SJAG_04369"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108816],"is_not":false,"summary":null,"term":"GO:0032296"},{"annotations":[59952,68096,73942,77024,60589],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004525"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of phosphodiester bonds in double-stranded RNA molecules.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA nuclease activity","termid":"GO:0004540"},{"relation_name":"is_a","term_name":"hydrolase activity, acting on ester bonds","termid":"GO:0016788"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01463":null,"SJAG_02156":null,"SJAG_03689":null,"SJAG_04019":null,"SJAG_04369":null,"SJAG_04527":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0016788","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"double-stranded RNA-specific ribonuclease activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"double-stranded RNA-specific RNase activity","type":"exact"},{"name":"dsRNA-specific RNase activity","type":"exact"},{"name":"dsRNA-specific ribonuclease activity","type":"exact"}],"termid":"GO:0032296","terms_by_termid":{"GO:0004525":null,"GO:0032296":null}}


id: GO:0032611
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-1 beta due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interleukin-1 production","termid":"GO:0032612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-1 beta production","secondary_identifiers":["GO:0050702","GO:0050720"],"synonyms":[{"name":"IL-1 beta production","type":"exact"},{"name":"interleukin-1 beta biosynthetic process","type":"narrow"},{"name":"interleukin-1 beta secretion","type":"narrow"}],"termid":"GO:0032611"}


id: MONDO:0000707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A colitis which can occur as a complication of ileostomy or colostomy.","direct_ancestors":[{"relation_name":"is_a","term_name":"colitis","termid":"MONDO:0005292"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"diversion colitis","secondary_identifiers":["MEDGEN:540758","DOID:0060187","icd11.foundation:553304993","ICD9:558.9","SCTID:51290000","UMLS:C0267532","ICD9:558"],"termid":"MONDO:0000707","xrefs":{"Monarch":{"xref_id":"0000707"}}}


id: MONDO:0017046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Peripheral neuroepithelioma is a rare noncentral nervous system tumor with evidence of primitive neuroectodermal differentiation.","definition_xrefs":["Orphanet:2677"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroepithelial neoplasm","termid":"MONDO:0021193"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroepithelioma","secondary_identifiers":["GARD:3963","icd11.foundation:841824628"],"termid":"MONDO:0017046","xrefs":{"Monarch":{"xref_id":"0017046"}}}


id: MONDO:0004913
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"esotropia","termid":"MONDO:0004896"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alternating esotropia","secondary_identifiers":["SCTID:39837002","icd11.foundation:935468618","UMLS:C0152205","DOID:9888","MEDGEN:57515","ICD9:378.05","ICD10CM:H50.05"],"termid":"MONDO:0004913","xrefs":{"Monarch":{"xref_id":"0004913"}}}


id: MONDO:0034943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete isolated vitreoretinopathy (obsolete MONDO:0034943)","secondary_identifiers":["Orphanet:519304"],"termid":"MONDO:0034943","xrefs":{"Monarch":{"xref_id":"0034943"}}}


id: PBO:0045648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox A pseudogene 6","termid":"PBO:0045648"}


id: GO:0034720
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the removal of a methyl group from lysine at position 4 of the histone.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K4 demethylation (obsolete GO:0034720)","synonyms":[{"name":"H3K4 demethylation (me1 me2 and me3)","type":"related"}],"termid":"GO:0034720"}


id: PATO:0001383
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A polyploidy quality inhering in a bearer by virtue of the bearer's containing five homologous sets of chromosomes.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Pentaploid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyploid","termid":"PATO:0001377"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pentaploid","termid":"PATO:0001383"}


id: GO:0046120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of any one of a family of organic molecules consisting of a purine or pyrimidine base covalently bonded to a sugar deoxyribose (a deoxyribonucleoside).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyribonucleoside metabolic process","termid":"GO:0009120"},{"relation_name":"is_a","term_name":"nucleoside biosynthetic process","termid":"GO:0009163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"deoxyribonucleoside biosynthetic process","synonyms":[{"name":"deoxyribonucleoside anabolism","type":"exact"},{"name":"deoxyribonucleoside biosynthesis","type":"exact"},{"name":"deoxyribonucleoside formation","type":"exact"},{"name":"deoxyribonucleoside synthesis","type":"exact"}],"termid":"GO:0046120"}


id: PBO:0113007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Asn rich cytoplasmic protein with a role in clathrin suppresion; contains RGG motifs; high-copy suppressor of group II intron-splicing defects of a mutation in MRS2 and of a conditional mutation in POL1 (DNA polymerase alpha); possible role in mitochondrial mRNA splicing","termid":"PBO:0113007"}


id: MONDO:0002322
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acquired degenerative dilation or expansion (ectasia) of normal blood vessels, often associated with aging. They are isolated, tortuous, thin-walled vessels and sources of bleeding. They occur most often in mucosal capillaries of the gastrointestinal tract leading to gastrointestinal hemorrhage and anemia.","definition_xrefs":["MESH:D016888"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiodysplasia","secondary_identifiers":["DOID:2494","UMLS:C0085411","MEDGEN:88403","ICD9:537.83","SCTID:90858003"],"synonyms":[{"name":"angiodysplasia of stomach and duodenum with haemorrhage","type":"narrow"},{"name":"angiodysplasia of stomach and duodenum with hemorrhage","type":"narrow"}],"termid":"MONDO:0002322","xrefs":{"Monarch":{"xref_id":"0002322"}}}


id: PBO:0088613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear HMG-like acidic protein Mak16","termid":"PBO:0088613"}


id: GO:0102793
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-alpha-D-glucuronate + soyasapogenol B = H+ + UDP + soyasapogenol B 3-O-beta-glucuronate.","definition_xrefs":["EC:2.4.1.262","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"soyasapogenol B glucuronosyltransferase activity","secondary_identifiers":["RHEA:31475","MetaCyc:RXN-8086"],"termid":"GO:0102793"}


id: GO:0003868
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-hydroxyphenylpyruvate + O2 = homogentisate + CO2.","definition_xrefs":["EC:1.13.11.27"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"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:0003824","GO:0003674"],"is_obsolete":false,"name":"4-hydroxyphenylpyruvate dioxygenase activity","secondary_identifiers":["MetaCyc:4-HYDROXYPHENYLPYRUVATE-DIOXYGENASE-RXN","RHEA:16189","Reactome:R-HSA-71163","UM-BBD_reactionID:r0298"],"synonyms":[{"name":"4-hydroxyphenylpyruvate hydroxylase activity","type":"related"},{"name":"4-hydroxyphenylpyruvate:oxygen oxidoreductase (hydroxylating, decarboxylating)","type":"related"},{"name":"4-hydroxyphenylpyruvic acid dioxygenase activity","type":"related"},{"name":"p-hydroxyphenylpyruvate dioxygenase activity","type":"related"},{"name":"p-hydroxyphenylpyruvate hydroxylase activity","type":"related"},{"name":"p-hydroxyphenylpyruvate oxidase activity","type":"related"},{"name":"p-hydroxyphenylpyruvic acid hydroxylase activity","type":"related"},{"name":"p-hydroxyphenylpyruvic hydroxylase activity","type":"related"},{"name":"p-hydroxyphenylpyruvic oxidase activity","type":"related"}],"termid":"GO:0003868"}


id: MONDO:0035237
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare subtype of pyoderma gangrenosum disease characterized by grouped vesicles that rapidly spread and coalesce to form large bullae, which evolve into ulcerations that have an erythematous peripheral halo and central necrosis, mainly affecting the upper limbs and face. Lymphoproliferative diseases are frequently associated, thus prognosis is often compromised.","definition_xrefs":["Orphanet:538869"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyoderma gangrenosum","termid":"MONDO:0018824"}],"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":"bullous pyoderma gangrenosum","secondary_identifiers":["ICD10CM:L88","GARD:22222","MEDGEN:590609","UMLS:C0406687"],"synonyms":[{"name":"Phemphigoid pyoderma gangrenosum","type":"exact"}],"termid":"MONDO:0035237","xrefs":{"Monarch":{"xref_id":"0035237"}}}


id: PBO:0043303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain containing 20A","termid":"PBO:0043303"}


id: PR:000050568
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A septation initiation network scaffold protein cdc11 (Schizosaccharomyces pombe) that lacks phosphorylated residues.","definition_xrefs":["PMID:11676915","PMID:12546793","PRO:DAN"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cdc11/UnPhos","pombase_gene_id":"SPCC1739.11c","synonyms":[{"name":"PomBase_original_PRO_term_name: septation initiation network scaffold protein cdc11 unphosphorylated form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-cdc11/PhosRes-","type":"exact"},{"name":"cdc11/UnPhos","type":"exact"},{"name":"cdc11p hypophosphorylated form (1) (Schizosaccharomyces pombe)","type":"related"}],"termid":"PR:000050568"}


id: MONDO:0024526
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Zimmermann-Laband syndrome in which the cause of the disease is a mutation in the KCNH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Zimmermann-Laband syndrome","termid":"MONDO:0000200"},{"relation_name":"is_a","term_name":"KCNH1 associated disorder","termid":"MONDO:0100485"}],"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":"Zimmermann-Laband syndrome 1","secondary_identifiers":["MEDGEN:1639277","NORD:1344","UMLS:C4551773","GARD:15071","OMIM:135500"],"synonyms":[{"name":"KCNH1 Zimmermann-Laband syndrome","type":"exact"},{"name":"Laband Syndrome","type":"exact"},{"name":"Laband syndrome","type":"related"},{"name":"ZLS1","type":"exact"},{"name":"Zimmermann-Laband syndrome 1","type":"exact"},{"name":"Zimmermann-Laband syndrome caused by mutation in KCNH1","type":"exact"},{"name":"fibromatosis, gingival, with abnormal fingers, fingernails, Nose, and ears, and splenomegaly","type":"related"}],"termid":"MONDO:0024526","xrefs":{"Monarch":{"xref_id":"0024526"}}}


id: GO:0047548
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-methyleneglutarate = 2-methylene-3-methylsuccinate.","definition_xrefs":["EC:5.4.99.4","RHEA:13793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"2-methyleneglutarate mutase activity","secondary_identifiers":["KEGG_REACTION:R03908","MetaCyc:2-METHYLENEGLUTARATE-MUTASE-RXN"],"synonyms":[{"name":"2-methyleneglutarate carboxy-methylenemethylmutase activity","type":"related"},{"name":"alpha-methyleneglutarate mutase activity","type":"related"}],"termid":"GO:0047548"}


id: MONDO:0021045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant neoplasm characterized by the presence of an epithelial and a fibrous component. Representative examples are fibroadenoma and phyllodes tumor.","definition_xrefs":["NCIT:C3743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mixed neoplasm","termid":"MONDO:0021043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroepithelial neoplasm","secondary_identifiers":["MESH:D018225","UMLS:C0206649","EFO:0007271","MEDGEN:104908"],"synonyms":[{"name":"fibroepithelial neoplasm","type":"exact"},{"name":"fibroepithelial tumor","type":"exact"},{"name":"fibroepithelial tumour","type":"exact"}],"termid":"MONDO:0021045","xrefs":{"Monarch":{"xref_id":"0021045"}}}


id: MONDO:1012521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bilateral deafness and vestibular dysfunction, non-human animal","termid":"MONDO:1011710"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bilateral deafness and vestibular dysfunction, pig","secondary_identifiers":["OMIA:002148-9823"],"termid":"MONDO:1012521","xrefs":{"Monarch":{"xref_id":"1012521"}}}


id: MONDO:0044716
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome (obsolete MONDO:0044716)","termid":"MONDO:0044716","xrefs":{"Monarch":{"xref_id":"0044716"}}}


id: PBO:0018183
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae HMG2 catalytic domain","termid":"PBO:0018183"}


id: PBO:0066229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 38","termid":"PBO:0066229"}


id: GO:0005177
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A class of ligands for neurexins.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete neuroligin (obsolete GO:0005177)","synonyms":[{"name":"neuroligin","type":"exact"}],"termid":"GO:0005177"}


id: PBO:0092011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial DNA binding endonuclease (intron encoded)","termid":"PBO:0092011"}


id: PBO:0081105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZEB1 transcriptional regulator RNA","termid":"PBO:0081105"}


id: MONDO:0032822
data:
  {"annotated_genes":["SJAG_05327"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87328],"is_not":false,"summary":null,"term":"MONDO:0032822"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"},{"relation_name":"is_a","term_name":"disorder of GPI anchor biosynthesis","termid":"MONDO:0024321"},{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05327":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525","MONDO:0700092","MONDO:0005027","MONDO:0024322","MONDO:0002320"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 80","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618580","DOID:0112216","UMLS:C5231418","MEDGEN:1684779"],"synonyms":[{"name":"DEE80","type":"exact"},{"name":"EIEE80","type":"exact"},{"name":"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 80","type":"exact"},{"name":"Glycosylphosphatidylinositol Biosynthesis Defect 20","type":"related"},{"name":"developmental and epileptic encephalopathy 80","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 80","type":"exact"}],"termid":"MONDO:0032822","terms_by_termid":{"MONDO:0032822":null},"xrefs":{"Monarch":{"xref_id":"0032822"}}}


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


id: PATO:0000185
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A behavioral quality inhering in a bearer by virtue of having physical steadiness.","definition_xrefs":["thefreedictionary:thefreedictionary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavioral quality","termid":"PATO:0000186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"balance","termid":"PATO:0000185"}


id: MONDO:0002054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete breast cancer (obsolete MONDO:0002054)","termid":"MONDO:0002054","xrefs":{"Monarch":{"xref_id":"0002054"}}}


id: PBO:0003554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic spindle checkpoint protein Mad1","termid":"PBO:0003554"}


id: GO:0010228
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process involved in transforming a meristem that produces vegetative structures, such as leaves, into a meristem that produces reproductive structures, such as a flower or an inflorescence.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"part_of","term_name":"post-embryonic development","termid":"GO:0009791"},{"relation_name":"part_of","term_name":"reproductive structure development","termid":"GO:0048608"}],"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":"vegetative to reproductive phase transition of meristem","synonyms":[{"name":"floral evocation","type":"related"},{"name":"flowering","type":"related"},{"name":"transition from vegetative to reproductive phase","type":"exact"}],"termid":"GO:0010228"}


id: PBO:0076358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin like 5","termid":"PBO:0076358"}


id: MONDO:0008310
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hutchinson-Gilford progeria syndrome is a rare, fatal, autosomal dominant and premature aging disease, beginning in childhood and characterized by growth reduction, failure to thrive, a typical facial appearance (prominent forehead, protuberant eyes, thin nose with a beaked tip, thin lips, micrognathia and protruding ears) and distinct dermatologic features (generalized alopecia, aged-looking skin, sclerotic and dimpled skin over the abdomen and extremities, prominent cutaneous vasculature, dyspigmentation, nail hypoplasia and loss of subcutaneous fat).","definition_xrefs":["Orphanet:740"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"primary osteolysis","termid":"MONDO:0019707"},{"relation_name":"is_a","term_name":"progeria","termid":"MONDO:0020732"},{"relation_name":"is_a","term_name":"laminopathy","termid":"MONDO:0021106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019303"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019303","MONDO:0006025"],"is_obsolete":false,"name":"Hutchinson-Gilford progeria syndrome","secondary_identifiers":["DOID:3911","ICD9:259.8","NANDO:2200833","NORD:1257","SCTID:238870004","UMLS:C0033300","GARD:7467","NANDO:1201007","MEDGEN:46123","MedDRA:10036794","OMIM:176670","NCIT:C34951"],"synonyms":[{"name":"HGPS","type":"exact"},{"name":"Hutchinson Gilford progeria syndrome","type":"related"},{"name":"Hutchinson Gilford syndrome","type":"exact"},{"name":"Hutchinson-Gilford disease","type":"exact"},{"name":"Hutchinson-Gilford progeria","type":"exact"},{"name":"Hutchinson-Gilford progeria syndrome","type":"exact"},{"name":"premature senility syndrome","type":"exact"},{"name":"progeria","type":"broad"},{"name":"progeria syndrome, childhood-onset","type":"related"}],"termid":"MONDO:0008310","xrefs":{"Monarch":{"xref_id":"0008310"}}}


id: PATO:0000045
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000045 absolute frequency (obsolete PATO:0000045)","termid":"PATO:0000045"}


id: GO:0014056
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of acetylcholine.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synaptic transmission, cholinergic","termid":"GO:0032222"},{"relation_name":"is_a","term_name":"regulation of neurotransmitter secretion","termid":"GO:0046928"},{"relation_name":"is_a","term_name":"regulation of amine transport","termid":"GO:0051952"},{"relation_name":"regulates","term_name":"acetylcholine secretion, neurotransmission","termid":"GO:0014055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of acetylcholine secretion, neurotransmission","termid":"GO:0014056"}


id: MONDO:0001914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare form of necrotizing anterior scleritis without pain in which the sclera is notably white, avascular and thin. Both choroidal exposure and staphyloma formation may occur.","direct_ancestors":[{"relation_name":"is_a","term_name":"necrotizing scleritis","termid":"MONDO:0040699"}],"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":"scleromalacia perforans","secondary_identifiers":["ICD9:379.04","SCTID:26664005","DOID:14230","icd11.foundation:740830358","UMLS:C0155354","MEDGEN:509929"],"termid":"MONDO:0001914","xrefs":{"Monarch":{"xref_id":"0001914"}}}


id: PBO:0049683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxyacylglutathione hydrolase like","termid":"PBO:0049683"}


id: PR:000050521
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-binding protein scr1 (Schizosaccharomyces pombe) that has not been phosphorylated at positions equivalent to Ser-235, Ser-332, Ser-333, Ser-408, and Ser-410 of the amino acid sequence represented by UniProtKB:O14335. Example: UniProtKB:O14335, Ser-235/Ser-332/Ser-333/Ser-408/Ser-410, PR:000026291.","definition_xrefs":["PomBase:VW","PRO:DAN","PMID:22140232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-binding protein scr1 (Schizosaccharomyces pombe)","termid":"PR:000050519"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scr1/UnPhos:(S236,S332,S333,S408,S410)","pombase_gene_id":"SPBC1D7.02c","synonyms":[{"name":"PomBase_original_PRO_term_name: DNA-binding protein scr1 unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-scr1/Phos:1","type":"exact"},{"name":"UniProtKB:O14335, Ser-235/Ser-332/Ser-333/Ser-408/Ser-410, PR:000026291","type":"narrow"},{"name":"scr1/UnPhos:(S236,S332,S333,S408,S410)","type":"exact"}],"termid":"PR:000050521"}


id: MOD:00090
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-alanine residue to L-alanine amide.","definition_xrefs":["PubMed:1377792","PubMed:8472537","PubMed:952951","PubMed:2069951","RESID:AA0081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-alanine residue","termid":"MOD:00901"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-alanine amide","synonyms":[{"name":"(2S)-2-aminopropanamide","type":"exact"},{"name":"AlaN","type":"exact"},{"name":"L-alanine amide","type":"exact"},{"name":"MOD_RES Alanine amide","type":"exact"},{"name":"alaninamide","type":"exact"},{"name":"amidated L-alanine","type":"exact"}],"termid":"MOD:00090"}


id: GO:0140290
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of ADP-ribose from ADP-ribosylserine.","definition_xrefs":["PMID:29234005","PMID:28650317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein de-ADP-ribosylation","termid":"GO:0051725"}],"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":"peptidyl-serine ADP-deribosylation","termid":"GO:0140290"}


id: PBO:0040294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2","termid":"PBO:0040294"}


id: PATO:0002067
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial pattern inhering in a bearer by virtue of the bearer's layered configuration.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spatial pattern","termid":"PATO:0000060"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stratification","termid":"PATO:0002067"}


id: PBO:0068140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 447","termid":"PBO:0068140"}


id: GO:0004086
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of a reaction that results in the formation of carbamoyl phosphate.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete carbamoyl-phosphate synthase activity (obsolete GO:0004086)","synonyms":[{"name":"carbamoyl phosphate synthase activity","type":"exact"},{"name":"carbamoyl-phosphate synthase activity","type":"exact"}],"termid":"GO:0004086"}


id: MONDO:0002648
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm in which there is infiltration of the skin overlying the breast by neoplastic large cells with abundant pale cytoplasm and large nuclei with prominent nucleoli (Paget cells). It is almost always associated with an intraductal or invasive ductal carcinoma of the breast. The clinical features include focal skin reddening, and eczema. Retraction of the nipple may sometimes occur.","definition_xrefs":["NCIT:C47857"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast adenocarcinoma","termid":"MONDO:0004988"},{"relation_name":"is_a","term_name":"Paget disease","termid":"MONDO:0021165"}],"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":"mammary Paget disease","secondary_identifiers":["UMLS:C0030185","ICDO:8540/3","DOID:3443","MEDGEN:18263","MESH:D010144"],"synonyms":[{"name":"Paget cell neoplasm","type":"exact"},{"name":"Paget disease of the breast","type":"exact"},{"name":"Paget's disease of breast","type":"exact"},{"name":"Paget's disease of the breast","type":"exact"},{"name":"breast Paget disease","type":"exact"},{"name":"mammary Paget disease","type":"exact"},{"name":"mammary Paget's disease","type":"exact"}],"termid":"MONDO:0002648","xrefs":{"Monarch":{"xref_id":"0002648"}}}


id: PBO:0006679
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Defective in SREBP Cleavage","termid":"PBO:0006679"}


id: GO:0048803
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of male genitalia are generated and organized from the genital imaginal disc.","definition_xrefs":["GOC:ai","GOC:sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc-derived genitalia morphogenesis","termid":"GO:0048805"},{"relation_name":"is_a","term_name":"male genitalia morphogenesis","termid":"GO:0048808"},{"relation_name":"part_of","term_name":"imaginal disc-derived male genitalia development","termid":"GO:0007485"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"imaginal disc-derived male genitalia morphogenesis","synonyms":[{"name":"male genital morphogenesis","type":"broad"}],"termid":"GO:0048803"}


id: PBO:0031574
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-small_vegetative_cell","termid":"PBO:0031574"}


id: GO:0006141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving purines.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nucleobase-containing compound metabolic process","termid":"GO:0019219"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"regulates","term_name":"purine nucleobase metabolic process","termid":"GO:0006144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"regulation of purine nucleobase metabolic process","synonyms":[{"name":"regulation of purine base metabolic process","type":"exact"},{"name":"regulation of purine base metabolism","type":"exact"}],"termid":"GO:0006141"}


id: GO:0048608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reproductive developmental process whose specific outcome is the progression of somatic structures that will be used in the process of creating new individuals from one or more parents, from their formation to the mature structures.","definition_xrefs":["GOC:jid","GOC:dph","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"reproductive system development","termid":"GO:0061458"}],"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":"reproductive structure development","termid":"GO:0048608"}


id: PBO:0055100
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 2518","termid":"PBO:0055100"}


id: PATO:0002113
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Perforated like a sieve.","definition_xrefs":["merriam-webster:merriam-webster"],"direct_ancestors":[{"relation_name":"is_a","term_name":"perforate","termid":"PATO:0002112"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cribriform","termid":"PATO:0002113"}


id: PBO:0066422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RALBP1 associated Eps domain containing 2","termid":"PBO:0066422"}


id: PBO:0068594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 45, pseudogene","termid":"PBO:0068594"}


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


id: MONDO:0008228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Megaloblastic anemia caused by vitamin B-12 deficiency due to impaired absorption. The impaired absorption of vitamin B-12 is secondary to atrophic gastritis and loss of gastric parietal cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"megaloblastic anemia","termid":"MONDO:0001700"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"nutritional deficiency disease","termid":"MONDO:0006873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"pernicious anemia","secondary_identifiers":["GARD:12671","UMLS:C0002892","ICD9:281.0","MEDGEN:1531","NCIT:C2871","Orphanet:120","DOID:13381","OMIM:170900","SCTID:84027009","EFO:0005576","MESH:D000752"],"synonyms":[{"name":"Addison anaemia","type":"exact"},{"name":"Addison anemia","type":"exact"},{"name":"Addison's anaemia","type":"exact"},{"name":"Addison's anemia","type":"exact"},{"name":"Addison-Biermer anaemia","type":"exact"},{"name":"Addison-Biermer anemia","type":"exact"},{"name":"Biermer anaemia","type":"exact"},{"name":"Biermer anemia","type":"exact"},{"name":"Biermer disease","type":"exact"},{"name":"Biermer's anaemia","type":"exact"},{"name":"Biermer's anemia","type":"exact"},{"name":"acquired pernicious anaemia","type":"exact"},{"name":"acquired pernicious anemia","type":"exact"},{"name":"anaemia pernicious","type":"exact"},{"name":"anemia pernicious","type":"exact"},{"name":"intrinsic factor deficiency","type":"exact"},{"name":"juvenile onset pernicious anaemia","type":"exact"},{"name":"juvenile onset pernicious anemia","type":"exact"},{"name":"pernicious anemia","type":"exact"}],"termid":"MONDO:0008228","xrefs":{"Monarch":{"xref_id":"0008228"}}}


id: SO:0000770
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The acceptor region of a two-piece tmRNA that when mature is charged at its 3' end with alanine. The tmRNA gene undergoes circular permutation in some groups of bacteria; processing of the transcripts from such a gene leaves the mature tmRNA in two pieces, base-paired together.","definition_xrefs":["Indiana:kw","doi:10.1093/nar/gkh795"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tmRNA_region","termid":"SO:0000847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tmRNA_acceptor_piece","synonyms":[{"name":"tmRNA acceptor piece","type":"exact"}],"termid":"SO:0000770"}


id: GO:0043100
data:
  {"annotated_genes":["SJAG_04354"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006223"}]},"cv_name":"biological_process","definition":"Any process that generates pyrimidine nucleobases, 1,3-diazine organic nitrogenous bases, from derivatives of them without de novo synthesis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine-containing compound salvage","termid":"GO:0008655"},{"relation_name":"is_a","term_name":"pyrimidine nucleobase biosynthetic process","termid":"GO:0019856"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04354":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"pyrimidine nucleobase salvage","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pyrimidine base salvage","type":"exact"}],"termid":"GO:0043100","terms_by_termid":{"GO:0006223":null}}


id: PBO:0060852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEK2 divergent transcript","termid":"PBO:0060852"}


id: PBO:0078853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRPC6 pseudogene 1","termid":"PBO:0078853"}


id: PBO:0052780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 19 pseudogene 3","termid":"PBO:0052780"}


id: GO:0046984
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of hemoglobin, an oxygen carrying, conjugated protein containing four heme groups and globin.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of macromolecule biosynthetic process","termid":"GO:0010556"},{"relation_name":"is_a","term_name":"regulation of protein metabolic process","termid":"GO:0051246"},{"relation_name":"regulates","term_name":"hemoglobin biosynthetic process","termid":"GO:0042541"}],"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 hemoglobin biosynthetic process","synonyms":[{"name":"regulation of haemoglobin biosynthesis","type":"exact"},{"name":"regulation of haemoglobin biosynthetic process","type":"exact"},{"name":"regulation of hemoglobin anabolism","type":"exact"},{"name":"regulation of hemoglobin biosynthesis","type":"exact"},{"name":"regulation of hemoglobin formation","type":"exact"},{"name":"regulation of hemoglobin synthesis","type":"exact"}],"termid":"GO:0046984"}


id: GO:0061303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the cornea over time, from its formation to the mature structure. The cornea is the transparent structure that covers the anterior of the eye.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"camera-type eye development","termid":"GO:0043010"}],"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":"cornea development in camera-type eye","termid":"GO:0061303"}


id: PBO:0089709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma tubulin complex GCP3 subunit Alp6","termid":"PBO:0089709"}


id: PBO:0085802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; copurifies with late Golgi vesicles containing the v-SNARE Tlg2p; PTM1 has a paralog, YHL017W, that arose from the whole genome duplication","termid":"PBO:0085802"}


id: PBO:0030245
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_ethanol","termid":"PBO:0030245"}


id: GO:2001096
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a cellotrioseacetate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trisaccharide transport","termid":"GO:2001088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"cellotriose transport","termid":"GO:2001096"}


id: PBO:0001110
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukoencephalopathy","termid":"PBO:0001110"}


id: PBO:0084723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane protein; required for assembly of cytochrome c oxidase","termid":"PBO:0084723"}


id: GO:1904303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of maternal process involved in parturition.","definition_xrefs":["PMID:1849751","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of maternal process involved in parturition","termid":"GO:1904301"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"maternal process involved in parturition","termid":"GO:0060137"}],"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 maternal process involved in parturition","synonyms":[{"name":"activation of maternal process involved in parturition","type":"narrow"},{"name":"up regulation of maternal process involved in parturition","type":"exact"},{"name":"up-regulation of maternal process involved in parturition","type":"exact"},{"name":"upregulation of maternal process involved in parturition","type":"exact"}],"termid":"GO:1904303"}


id: PBO:0002739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human ZNF277 ortholog","termid":"PBO:0002739"}


id: PBO:0059357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S17 pseudogene 1","termid":"PBO:0059357"}


id: GO:0032674
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-5 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-5 production","termid":"GO:0032634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of interleukin-5 production","secondary_identifiers":["GO:2000662","GO:0045405"],"synonyms":[{"name":"regulation of IL-5 production","type":"exact"},{"name":"regulation of interleukin-5 biosynthetic process","type":"narrow"},{"name":"regulation of interleukin-5 secretion","type":"narrow"}],"termid":"GO:0032674"}


id: MONDO:0011813
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"postaxial polydactyly type A","termid":"MONDO:0019673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polydactyly, postaxial, type A3","secondary_identifiers":["UMLS:C1846452","GARD:18174","MEDGEN:337585","MESH:C564590","OMIM:607324"],"synonyms":[{"name":"PAPA3","type":"related"},{"name":"Papa3","type":"related"},{"name":"polydactyly, postaxial, type A3","type":"exact"},{"name":"postaxial polydactyly, type A3","type":"related"}],"termid":"MONDO:0011813","xrefs":{"Monarch":{"xref_id":"0011813"}}}


id: GO:0050323
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: A + H2O + taurine = AH(2) + NH4 + sulfoacetaldehyde.","definition_xrefs":["RHEA:18709","PMID:15073291"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors","termid":"GO:0016638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"taurine dehydrogenase activity","secondary_identifiers":["EC:1.4.99.2","KEGG_REACTION:R07167","MetaCyc:TAURINE-DEHYDROGENASE-RXN"],"synonyms":[{"name":"taurine:(acceptor) oxidoreductase (deaminating)","type":"related"},{"name":"taurine:acceptor oxidoreductase (deaminating)","type":"related"}],"termid":"GO:0050323"}


id: FYPO:0000876
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 dimethylation of lysine at position 9 of histone H3 occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 dimethylation during vegetative growth","termid":"FYPO:0000866"},{"relation_name":"is_a","term_name":"decreased histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002274","FYPO:0002494","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone H3-K9 dimethylation during vegetative growth","synonyms":[{"name":"decreased histone H3 K9 dimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 dimethylation during mitotic cell cycle","type":"related"},{"name":"decreased histone H3K9 dimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3K9me2 during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K9 dimethylation during vegetative growth","type":"exact"},{"name":"reduced histone H3-K9 dimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000876"}


id: PBO:0040906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 10","termid":"PBO:0040906"}


id: MONDO:0014179
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any inclusion body myopathy with Paget disease of bone and frontotemporal dementia in which the cause of the disease is a mutation in the HNRNPA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inclusion body myopathy with Paget disease of bone and frontotemporal dementia","termid":"MONDO:0000507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3","secondary_identifiers":["MEDGEN:815799","UMLS:C3809469","DOID:0111386","GARD:15963","OMIM:615424"],"synonyms":[{"name":"HNRNPA1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia","type":"exact"},{"name":"IBMPFD3","type":"related"},{"name":"inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA1","type":"exact"},{"name":"inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3","type":"exact"},{"name":"inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 3","type":"exact"},{"name":"inclusion body myopathy with early-onset paget disease without frontotemporal dementia 3","type":"exact"},{"name":"multisystem Proteinopathy 3","type":"related"}],"termid":"MONDO:0014179","xrefs":{"Monarch":{"xref_id":"0014179"}}}


id: GO:0050119
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acetyl-D-glucosamine + H2O = D-glucosamine + acetate.","definition_xrefs":["RHEA:20593","EC:3.5.1.33"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"},{"relation_name":"is_a","term_name":"deacetylase activity","termid":"GO:0019213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016810","GO:0003824","GO:0003674","GO:0019213","GO:0016787"],"is_obsolete":false,"name":"N-acetylglucosamine deacetylase activity","secondary_identifiers":["KEGG_REACTION:R01200","MetaCyc:N-ACETYLGLUCOSAMINE-DEACETYLASE-RXN","Reactome:R-HSA-2022887"],"synonyms":[{"name":"N-acetyl-D-glucosamine amidohydrolase activity","type":"related"},{"name":"N-acetyl-D-glucosaminyl N-deacetylase activity","type":"related"},{"name":"acetylaminodeoxyglucose acetylhydrolase activity","type":"related"}],"termid":"GO:0050119"}


id: PBO:0074272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schlafen family member 13","termid":"PBO:0074272"}


id: PBO:0073489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shugoshin 1 pseudogene 2","termid":"PBO:0073489"}


id: PBO:0070886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15 pseudogene 18","termid":"PBO:0070886"}


id: GO:0046620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of growth of an organ of an organism.","definition_xrefs":["GOC:tb","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"organ growth","termid":"GO:0035265"}],"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 organ growth","termid":"GO:0046620"}


id: PBO:0088515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S7","termid":"PBO:0088515"}


id: PBO:0031139
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_actomyosin_contractile_ring_myosin_filament_organization","termid":"PBO:0031139"}


id: PBO:0027532
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ribonuclease_activity","termid":"PBO:0027532"}


id: PBO:0062379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily D member 1 pseudogene","termid":"PBO:0062379"}


id: PBO:0085870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; highly induced in zinc-depleted conditions and has increased expression in NAP1 deletion mutants; VEL1 has a paralog, YOR387C, that arose from a single-locus duplication","termid":"PBO:0085870"}


id: MONDO:1012977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital hypotrichosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital hypotrichosis, non-human animal","termid":"MONDO:1012977","xrefs":{"Monarch":{"xref_id":"1012977"}}}


id: GO:0016790
data:
  {"annotated_genes":["SJAG_00944","SJAG_02769","SJAG_02985","SJAG_04107","SJAG_04895","SJAG_01396","SJAG_01596","SJAG_00774","SJAG_02268","SJAG_00734","SJAG_03377","SJAG_02056","SJAG_04007","SJAG_00902"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003860"},{"annotations":[75889,77125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003986"},{"annotations":[59918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016297"},{"annotations":[97140,80698,107794,101962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047617"},{"annotations":[73551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004416"},{"annotations":[80631,70489,61587,93844,101260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008474"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: RCO-SR' + H2O = RCOOH + HSR'. This reaction is the hydrolysis of a thiolester bond, an ester formed from a carboxylic acid and a thiol (i.e., RCO-SR'), such as that found in acetyl-coenzyme A.","definition_xrefs":["EC:3.1.2.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on ester bonds","termid":"GO:0016788"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00734":null,"SJAG_00774":null,"SJAG_00902":null,"SJAG_00944":null,"SJAG_01396":null,"SJAG_01596":null,"SJAG_02056":null,"SJAG_02268":null,"SJAG_02769":null,"SJAG_02985":null,"SJAG_03377":null,"SJAG_04007":null,"SJAG_04107":null,"SJAG_04895":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016788","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"thiolester hydrolase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"thiolesterase activity","type":"exact"}],"termid":"GO:0016790","terms_by_termid":{"GO:0003860":null,"GO:0003986":null,"GO:0004416":null,"GO:0008474":null,"GO:0016297":null,"GO:0047617":null}}


id: FYPO:0000927
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which horsetail movement does not occur. 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"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"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:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abolished horsetail movement","synonyms":[{"name":"absent horsetail movement","type":"exact"},{"name":"dynein-driven meiotic oscillatory nuclear movement abolished","type":"exact"},{"name":"horsetail movement abolished","type":"exact"},{"name":"horsetail nuclear movement abolished","type":"exact"}],"termid":"FYPO:0000927"}


id: PBO:0030272
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_negative_regulation_of_mitotic_DNA_replication_initiation_resulting_in_partial_rereplication","termid":"PBO:0030272"}


id: GO:1990557
data:
  {"annotated_genes":["SJAG_00671"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88734],"is_not":false,"summary":null,"term":"GO:1990557"}]},"cv_name":"biological_process","definition":"The process in which sulfate is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:10428783"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfate transmembrane transport","termid":"GO:1902358"},{"relation_name":"is_a","term_name":"mitochondrial transmembrane transport","termid":"GO:1990542"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00671":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"mitochondrial sulfate transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990557","terms_by_termid":{"GO:1990557":null}}


id: PBO:0005068
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.38","termid":"PBO:0005068"}


id: PBO:0014232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canto_session","termid":"PBO:0014232"}


id: GO:1990275
data:
  {"annotated_genes":["SJAG_04599"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71395],"is_not":false,"summary":null,"term":"GO:1990275"}]},"cv_name":"molecular_function","definition":"Binding to a preribosome.","definition_xrefs":["PMID:22735702","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoprotein complex binding","termid":"GO:0043021"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04599":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"preribosome binding","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:1990275","terms_by_termid":{"GO:1990275":null}}


id: FYPO:0002019
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells form telomeres that are longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal telomere length during vegetative growth","termid":"FYPO:0006464"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000293"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000641","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000293"],"is_obsolete":false,"name":"elongated telomeres during vegetative growth","synonyms":[{"name":"elongated telomeres during mitotic cell cycle","type":"related"},{"name":"increased telomere length during vegetative growth","type":"exact"},{"name":"long telomeres during vegetative growth","type":"exact"}],"termid":"FYPO:0002019"}


id: MONDO:0000901
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse large B-cell lymphoma characterized by less than 50 percent decrease in lesion size with induction therapy or the appearance of new lesions or the appearance of new lesions after attainment of complete remission.","definition_xrefs":["DOID:0080192","PMID:22160081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"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":"relapsed/refractory diffuse large B-cell lymphoma","secondary_identifiers":["UMLS:C0855112","MEDGEN:208957"],"termid":"MONDO:0000901","xrefs":{"Monarch":{"xref_id":"0000901"}}}


id: GO:1905934
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cell fate determination.","definition_xrefs":["GOC:bhm","GOC:TermGenie","PMID:25793578","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate commitment","termid":"GO:0010454"},{"relation_name":"is_a","term_name":"regulation of cell fate determination","termid":"GO:1905933"},{"relation_name":"negatively_regulates","term_name":"cell fate determination","termid":"GO:0001709"}],"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 cell fate determination","synonyms":[{"name":"down regulation of cell fate determination","type":"exact"},{"name":"down-regulation of cell fate determination","type":"exact"},{"name":"downregulation of cell fate determination","type":"exact"},{"name":"inhibition of cell fate determination","type":"narrow"}],"termid":"GO:1905934"}


id: GO:0140255
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to phosphate starvation.","definition_xrefs":["PMID:29414789"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to nutrient levels","termid":"GO:0032107"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"cellular response to phosphate starvation","termid":"GO:0016036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cellular response to phosphate starvation","termid":"GO:0140255"}


id: PBO:0087805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tap42p-interacting protein; negative regulator of the TORC1 signaling pathway that activates the type 2A-related phosphatase Sit4p by binding and antagonizing Tap42p, a SIT4 inhibitor; proposed to be part of a feedback loop to amplify Sit4p activity when TORC1 is inactivated; protein abundance increases in response to DNA replication stress","termid":"PBO:0087805"}


id: FYPO:0002928
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which polyadenylated RNA molecules have poly(A) tails of normal (i.e. indistinguishable from wild type) length.","definition_xrefs":["PomBase:mah","PMID:24081329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257"],"is_obsolete":false,"name":"normal poly(A) tail length","synonyms":[{"name":"normal polyA sequence length","type":"exact"},{"name":"normal polyA tail length","type":"exact"}],"termid":"FYPO:0002928"}


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:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0000002"],"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:0074271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schlafen family member 12 like","termid":"PBO:0074271"}


id: FYPO:0007738
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 distribution of a protein localized to chromatin at the 3' ends of genes that can be transcribed by RNA polymerase II is normal (i.e. indistinguishable from wild type) during metaphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah","PMID:33771877"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin at 3' end of genes","termid":"FYPO:0007731"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to chromatin at 3' end of RNA polymerase II-transcribed genes during mitotic metaphase","synonyms":[{"name":"normal condensin localization to chromatin at 3' end of RNA polymerase II-transcribed genes during mitotic metaphase","type":"broad"},{"name":"normal protein localisation to chromatin at 3' end of RNA polymerase II-transcribed genes during mitotic metaphase","type":"exact"},{"name":"normal protein localization to chromatin at 3' end of RNA polymerase II-transcribed genes during metaphase during vegetative growth","type":"exact"},{"name":"normal protein localization to chromatin at 3' end of RNA polymerase II-transcribed genes during metaphase of mitotic cell cycle","type":"exact"},{"name":"normal protein localization to chromatin downstream of RNA polymerase II-transcribed genes during mitotic metaphase","type":"exact"}],"termid":"FYPO:0007738"}


id: PBO:0046657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESF1 nucleolar pre-rRNA processing protein homolog","termid":"PBO:0046657"}


id: PR:000027720
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ribonucleoside-diphosphate reductase complex in Schizosaccharomyces pombe that is composed of two small (suc22) subunits and two large (cdc22) subunits.","definition_xrefs":["PMID:20516199","PMID:8479429","PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonucleoside-diphosphate reductase complex (Schizosaccharomyces pombe)","synonyms":[{"name":"fission yeast RNR","type":"exact"},{"name":"fission yeast ribonucleotide reductase complex","type":"exact"}],"termid":"PR:000027720"}


id: PBO:0070226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 160 pseudogene","termid":"PBO:0070226"}


id: MONDO:0017781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 12p deletion","termid":"MONDO:0022174"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"12p12.1 microdeletion syndrome","secondary_identifiers":["MEDGEN:1652598","Orphanet:313884","GARD:17414","UMLS:C4755260"],"synonyms":[{"name":"Del(12)(p12.1)","type":"exact"},{"name":"monosomy 12p12.1","type":"exact"}],"termid":"MONDO:0017781","xrefs":{"Monarch":{"xref_id":"0017781"}}}


id: GO:0050337
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: thiosulfate + 2 glutathione = glutathione disulfide + hydrogen sulfide + sulfite + 2 H+.","definition_xrefs":["RHEA:14505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfurtransferase activity","termid":"GO:0016783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016782","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"thiosulfate-thiol sulfurtransferase activity","secondary_identifiers":["Reactome:R-HSA-1655879","MetaCyc:THIOSULFATE--THIOL-SULFURTRANSFERASE-RXN","EC:2.8.1.3"],"synonyms":[{"name":"glutathione-dependent thiosulfate reductase activity","type":"related"},{"name":"sulfane reductase activity","type":"related"},{"name":"sulfane sulfurtransferase activity","type":"related"},{"name":"thiosulfate:thiol sulfurtransferase activity","type":"related"},{"name":"thiosulphate-thiol sulphurtransferase activity","type":"exact"}],"termid":"GO:0050337"}


id: PR:O74561
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC970.08 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74561"],"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 inositol polyphosphate kinase C970.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC970.08","synonyms":[{"name":"Spom972h-SPCC970.08","type":"exact"}],"termid":"PR:O74561"}


id: GO:0050609
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + NAD+ + phosphonate = 2 H+ + NADH + phosphate.","definition_xrefs":["EC:1.20.1.1","RHEA:13173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on phosphorus or arsenic in donors, with NAD(P)+ as acceptor","termid":"GO:0050499"}],"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:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"phosphonate dehydrogenase activity","secondary_identifiers":["UM-BBD_reactionID:r1055","KEGG_REACTION:R05746","MetaCyc:1.20.1.1-RXN"],"synonyms":[{"name":"NAD-dependent phosphite dehydrogenas activity","type":"related"},{"name":"NAD:phosphite oxidoreductase activity","type":"related"},{"name":"phosphite dehydrogenase activity","type":"related"},{"name":"phosphonate:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0050609"}


id: MONDO:0010552
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":"Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita","secondary_identifiers":["MESH:C538077","OMIM:302803","UMLS:C1844864","MEDGEN:337105"],"synonyms":[{"name":"Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita","type":"exact"}],"termid":"MONDO:0010552","xrefs":{"Monarch":{"xref_id":"0010552"}}}


id: GO:0003743
data:
  {"annotated_genes":["SJAG_03678","SJAG_03223","SJAG_03996","SJAG_02628","SJAG_01643","SJAG_04900","SJAG_01117","SJAG_04981","SJAG_01954","SJAG_02390","SJAG_01659","SJAG_03629","SJAG_00507","SJAG_00466","SJAG_03732","SJAG_04635","SJAG_01576","SJAG_00786","SJAG_04891","SJAG_00662","SJAG_04744","SJAG_02995","SJAG_02164","SJAG_02376","SJAG_02307","SJAG_02471","SJAG_03788","SJAG_03433","SJAG_01487","SJAG_03472","SJAG_03147","SJAG_05003","SJAG_02856","SJAG_04772"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58152,59606,60532,61419,62059,63939,68766,71757,71960,72241,72262,72587,72736,72749,74257,74443,74687,74835,75156,75431,75996,76892,77788,77792,77978,78283,78837,79334,80446,87841,93100,105915,105940,115949],"is_not":false,"summary":null,"term":"GO:0003743"}]},"cv_name":"molecular_function","definition":"Functions in the initiation of ribosome-mediated translation of mRNA into a polypeptide.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation factor activity","termid":"GO:0180051"}],"gene_count":34,"genes_by_uniquename":{"SJAG_00466":null,"SJAG_00507":null,"SJAG_00662":null,"SJAG_00786":null,"SJAG_01117":null,"SJAG_01487":null,"SJAG_01576":null,"SJAG_01643":null,"SJAG_01659":null,"SJAG_01954":null,"SJAG_02164":null,"SJAG_02307":null,"SJAG_02376":null,"SJAG_02390":null,"SJAG_02471":null,"SJAG_02628":null,"SJAG_02856":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03223":null,"SJAG_03433":null,"SJAG_03472":null,"SJAG_03629":null,"SJAG_03678":null,"SJAG_03732":null,"SJAG_03788":null,"SJAG_03996":null,"SJAG_04635":null,"SJAG_04744":null,"SJAG_04772":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04981":null,"SJAG_05003":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"translation initiation factor activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-72621","GO:0003745","GO:0003744","Reactome:R-HSA-72697","Reactome:R-HSA-72722"],"termid":"GO:0003743","terms_by_termid":{"GO:0003743":null}}


id: PBO:0046936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 53 member B","termid":"PBO:0046936"}


id: PBO:0028878
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H2B-K119_ubiquitination","termid":"PBO:0028878"}


id: GO:0002890
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of an immunoglobulin mediated immune response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of B cell mediated immunity","termid":"GO:0002713"},{"relation_name":"is_a","term_name":"regulation of immunoglobulin mediated immune response","termid":"GO:0002889"},{"relation_name":"negatively_regulates","term_name":"immunoglobulin mediated immune response","termid":"GO:0016064"}],"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 immunoglobulin mediated immune response","synonyms":[{"name":"down regulation of immunoglobulin mediated immune response","type":"exact"},{"name":"down-regulation of immunoglobulin mediated immune response","type":"exact"},{"name":"downregulation of immunoglobulin mediated immune response","type":"exact"},{"name":"inhibition of immunoglobulin mediated immune response","type":"narrow"}],"termid":"GO:0002890"}


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


id: MONDO:0003736
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An overwhelming, irrational, and persistent fear of being diagnosed with cancer.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nosophobia","termid":"MONDO:0000600"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancerophobia","secondary_identifiers":["DOID:602","MEDGEN:115929","NCIT:C35492","UMLS:C0233705"],"synonyms":[{"name":"Cancerphobia","type":"exact"},{"name":"cancer phobia","type":"exact"},{"name":"fear of getting cancer","type":"exact"},{"name":"fear of getting cancer (finding)","type":"exact"}],"termid":"MONDO:0003736","xrefs":{"Monarch":{"xref_id":"0003736"}}}


id: PBO:0053045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"La ribonucleoprotein 4B","termid":"PBO:0053045"}


id: PBO:0111301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U1 snRNP-associated protein Prp39","termid":"PBO:0111301"}


id: PBO:0077031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"threonine synthase like 2","termid":"PBO:0077031"}


id: MONDO:0007321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant form of chondrodysplasia punctata.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"non-rhizomelic chondrodysplasia punctata","termid":"MONDO:0015775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant chondrodysplasia punctata","secondary_identifiers":["MONDO:0022728","Orphanet:79344","DOID:0060293","MEDGEN:303176","MESH:C563248","GARD:1298","OMIM:118650","UMLS:C1442935"],"synonyms":[{"name":"chondrodysplasia punctata Sheffield type","type":"exact"},{"name":"chondrodysplasia punctata due to vitamin K deficiency","type":"related"},{"name":"chondrodysplasia punctata due to warfarin teratogenicity","type":"related"},{"name":"chondrodysplasia punctata, Sheffield type","type":"exact"},{"name":"chondrodysplasia punctata, autosomal dominant","type":"exact"}],"termid":"MONDO:0007321","xrefs":{"Monarch":{"xref_id":"0007321"}}}


id: PBO:0090690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tricalbin, C2 domain protein (phospholipid binding) ER-plasma membrane tethering protein Tcb1","termid":"PBO:0090690"}


id: GO:0051587
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that prevents the activation of the directed movement of dopamine into a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of dopamine uptake involved in synaptic transmission","termid":"GO:0051585"},{"relation_name":"is_a","term_name":"inhibition of neurotransmitter uptake","termid":"GO:0051609"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"inhibition of dopamine uptake involved in synaptic transmission","synonyms":[{"name":"inhibition of dopamine import involved in synaptic transmission","type":"exact"}],"termid":"GO:0051587"}


