# terms

id: GO:0045666
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of neuron differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of neuron differentiation","termid":"GO:0045664"},{"relation_name":"positively_regulates","term_name":"neuron differentiation","termid":"GO:0030182"}],"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 neuron differentiation","synonyms":[{"name":"activation of neuron differentiation","type":"narrow"},{"name":"stimulation of neuron differentiation","type":"narrow"},{"name":"up regulation of neuron differentiation","type":"exact"},{"name":"up-regulation of neuron differentiation","type":"exact"},{"name":"upregulation of neuron differentiation","type":"exact"}],"termid":"GO:0045666"}


id: PBO:0069041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 286, pseudogene","termid":"PBO:0069041"}


id: PBO:0011481
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defect of the gene silencing at centromeric heterochromatin","termid":"PBO:0011481"}


id: GO:0007172
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a complex capable of relaying a signal within a cell.","definition_xrefs":["GOC:signaling","GOC:bf","PMID:9646862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0023052","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"signal complex assembly","synonyms":[{"name":"signal complex formation","type":"exact"}],"termid":"GO:0007172"}


id: MONDO:0014880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Duane syndrome type 3 is a disorder of eye movement.The affected eye, or eyes, has limited ability to move both inward toward the nose and outward toward the ears. The eye opening narrows and the eyeball pulls in when looking inward toward the nose. About 15 percent of all cases of Duane syndrome are type 3. Most cases occur without other signs and symptoms.In most people with Duane syndrome type 3, the cause is unknown; but it can sometimes be caused by mutations in the CHN1 gene and inherited in an autosomal dominant fashion.","definition_xrefs":["GARD:0010691"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Duane retraction syndrome","termid":"MONDO:0007473"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Duane retraction syndrome 3 with or without deafness","secondary_identifiers":["OMIM:617041","MEDGEN:934719","GARD:10691","UMLS:C4310752"],"synonyms":[{"name":"DURS3","type":"exact"},{"name":"Duane retraction syndrome 3","type":"related"},{"name":"Duane retraction syndrome 3 with or without deafness","type":"exact"},{"name":"Duane retraction syndrome caused by mutation in MAFB","type":"exact"},{"name":"Duane syndrome type 3","type":"related"},{"name":"MAFB Duane retraction syndrome","type":"exact"}],"termid":"MONDO:0014880","xrefs":{"Monarch":{"xref_id":"0014880"}}}


id: FYPO:0006113
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","gene_count":0,"genotype_count":0,"name":"obsolete increased chromatin-associated RNA level (obsolete FYPO:0006113)","termid":"FYPO:0006113"}


id: PBO:0060411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-alpha-acetyltransferase 38, NatC auxiliary subunit","termid":"PBO:0060411"}


id: PBO:0058444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5009","termid":"PBO:0058444"}


id: PBO:0076939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFIP11 divergent transcript","termid":"PBO:0076939"}


id: PBO:0001213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ornithine cyclodeaminase family (predicted)","termid":"PBO:0001213"}


id: MONDO:0010630
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":"imprinting gene related to retinoblastoma","secondary_identifiers":["OMIM:308290","MEDGEN:333451","UMLS:C1839964"],"synonyms":[{"name":"imprinting gene related to retinoblastoma","type":"exact"}],"termid":"MONDO:0010630","xrefs":{"Monarch":{"xref_id":"0010630"}}}


id: GO:0023052
data:
  {"annotated_genes":["SJAG_03753","SJAG_04471","SJAG_00574","SJAG_03940","SJAG_04259","SJAG_00526","SJAG_02342","SJAG_02923","SJAG_02278","SJAG_04668","SJAG_04262","SJAG_03384","SJAG_03987","SJAG_01983","SJAG_01677","SJAG_03089","SJAG_04671","SJAG_04486","SJAG_00996","SJAG_00429","SJAG_00329","SJAG_01150","SJAG_00790","SJAG_03793","SJAG_02945","SJAG_02486","SJAG_02468","SJAG_03209","SJAG_03081","SJAG_02426","SJAG_03927","SJAG_00845","SJAG_02013","SJAG_03936","SJAG_02232","SJAG_04551","SJAG_03501","SJAG_00551","SJAG_00143","SJAG_03137","SJAG_00649","SJAG_03340","SJAG_04537","SJAG_03345","SJAG_01821","SJAG_02878","SJAG_01799","SJAG_04126","SJAG_00600","SJAG_03342","SJAG_03720","SJAG_03126","SJAG_01873","SJAG_04552","SJAG_01187","SJAG_02684","SJAG_01516","SJAG_01000","SJAG_02712","SJAG_03695","SJAG_02392","SJAG_01376","SJAG_00640","SJAG_00439","SJAG_00369","SJAG_02098","SJAG_01270","SJAG_02380","SJAG_00883","SJAG_01855","SJAG_04455","SJAG_03568","SJAG_01082","SJAG_02424","SJAG_00623","SJAG_03508","SJAG_04871","SJAG_01768","SJAG_06270","SJAG_03072","SJAG_00402","SJAG_02854","SJAG_00610","SJAG_00078","SJAG_04573","SJAG_03310","SJAG_01679","SJAG_01667","SJAG_05290","SJAG_00256","SJAG_01245","SJAG_01181","SJAG_02514","SJAG_01146","SJAG_03353","SJAG_03611","SJAG_00100","SJAG_02336","SJAG_02074","SJAG_00071","SJAG_02311","SJAG_00824","SJAG_00226","SJAG_00266","SJAG_02135","SJAG_01632","SJAG_00875","SJAG_04910","SJAG_04496","SJAG_02000","SJAG_03371","SJAG_02321","SJAG_00486","SJAG_06592","SJAG_04522","SJAG_06588","SJAG_03376","SJAG_02771","SJAG_01401","SJAG_04457","SJAG_04509","SJAG_03887","SJAG_06621","SJAG_04943","SJAG_02231","SJAG_02249","SJAG_04426","SJAG_00296","SJAG_01605","SJAG_01307","SJAG_02318","SJAG_01386","SJAG_03529","SJAG_04329","SJAG_01138","SJAG_00781","SJAG_02169","SJAG_05030","SJAG_03026","SJAG_04507","SJAG_00690","SJAG_03090","SJAG_00318","SJAG_01901","SJAG_01286","SJAG_00092","SJAG_01885","SJAG_03319","SJAG_01837","SJAG_02266","SJAG_02858","SJAG_02429","SJAG_03309","SJAG_01184","SJAG_03048","SJAG_02027","SJAG_02404","SJAG_03248","SJAG_04776","SJAG_01699","SJAG_03802","SJAG_01754","SJAG_00293","SJAG_01519","SJAG_02682","SJAG_00530","SJAG_00317","SJAG_03421","SJAG_03969","SJAG_04884","SJAG_03637","SJAG_04464","SJAG_03591","SJAG_04268","SJAG_01774","SJAG_01464","SJAG_03488","SJAG_01373","SJAG_04461","SJAG_04987","SJAG_03681","SJAG_03623","SJAG_01020","SJAG_01253","SJAG_04232","SJAG_02921","SJAG_00509","SJAG_03655","SJAG_03879","SJAG_01188","SJAG_01205","SJAG_04140","SJAG_04052","SJAG_00340","SJAG_04283","SJAG_04777","SJAG_00214","SJAG_04771","SJAG_04597","SJAG_03386","SJAG_01657","SJAG_02104","SJAG_00534","SJAG_00356","SJAG_05373","SJAG_03185","SJAG_02022","SJAG_05335","SJAG_01429","SJAG_02258","SJAG_01978","SJAG_02765","SJAG_03942","SJAG_04312","SJAG_03557","SJAG_04026","SJAG_02183","SJAG_05184","SJAG_03302","SJAG_04332","SJAG_01047","SJAG_03854","SJAG_04765","SJAG_02072","SJAG_04460","SJAG_03709","SJAG_04280","SJAG_00167","SJAG_03067","SJAG_03355","SJAG_04249","SJAG_00661","SJAG_05978","SJAG_04018","SJAG_02703","SJAG_02723","SJAG_01254","SJAG_03907","SJAG_04825","SJAG_04083","SJAG_04465","SJAG_00333","SJAG_03525","SJAG_01790","SJAG_00027","SJAG_03405","SJAG_01076","SJAG_01716","SJAG_03928","SJAG_03931","SJAG_00082","SJAG_01330","SJAG_00209","SJAG_00963","SJAG_04128","SJAG_02576","SJAG_00993","SJAG_02536","SJAG_00457","SJAG_02838","SJAG_00331","SJAG_01509","SJAG_01345","SJAG_03160","SJAG_01161","SJAG_00975","SJAG_03453","SJAG_04383","SJAG_04103","SJAG_00514","SJAG_04235","SJAG_02498","SJAG_01084","SJAG_03678","SJAG_00321","SJAG_02472","SJAG_02433","SJAG_02203","SJAG_04462","SJAG_00229","SJAG_03486","SJAG_00688","SJAG_00472","SJAG_01825","SJAG_02026","SJAG_03073","SJAG_01210","SJAG_00169","SJAG_01906","SJAG_01213","SJAG_01010","SJAG_04999","SJAG_02760","SJAG_01320","SJAG_03602","SJAG_03705","SJAG_03438","SJAG_01114","SJAG_00561","SJAG_01297","SJAG_00142","SJAG_02058","SJAG_04412","SJAG_02601","SJAG_00236","SJAG_05330","SJAG_03748","SJAG_03625","SJAG_01311","SJAG_02736","SJAG_04503","SJAG_00424","SJAG_06622","SJAG_01805","SJAG_03592","SJAG_00807","SJAG_02481","SJAG_00642","SJAG_00364","SJAG_01199","SJAG_01118","SJAG_02379","SJAG_03272","SJAG_03624","SJAG_00704","SJAG_04118","SJAG_04435","SJAG_01587","SJAG_04394","SJAG_04968","SJAG_01718","SJAG_00028","SJAG_04384","SJAG_04151","SJAG_01044","SJAG_00210","SJAG_02819","SJAG_02233","SJAG_04873","SJAG_00678","SJAG_04206","SJAG_02389","SJAG_04980","SJAG_03799","SJAG_03263","SJAG_04468","SJAG_00823","SJAG_04287","SJAG_01787","SJAG_02444","SJAG_04655","SJAG_03898","SJAG_05304","SJAG_04638","SJAG_00681","SJAG_03739","SJAG_03828","SJAG_02451","SJAG_02592","SJAG_00327","SJAG_03631","SJAG_02366","SJAG_04343","SJAG_00718","SJAG_01585","SJAG_00289","SJAG_01032","SJAG_00991","SJAG_01680","SJAG_01708","SJAG_03893","SJAG_02289","SJAG_02520","SJAG_00858","SJAG_04469","SJAG_03338","SJAG_03482","SJAG_04734","SJAG_02563","SJAG_04666","SJAG_04761","SJAG_00114","SJAG_05000","SJAG_02823","SJAG_00117","SJAG_00990","SJAG_02785","SJAG_03361","SJAG_05286","SJAG_04200","SJAG_05346","SJAG_01142","SJAG_01703","SJAG_03841","SJAG_03903","SJAG_02860","SJAG_03327","SJAG_04699","SJAG_00216","SJAG_01040","SJAG_02605","SJAG_01942","SJAG_04920","SJAG_00244"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87230,87247,87546,87573,89327,91115,91527,91672,92023,92319,92486,93149,93246,95341,96694,96893,97198,97358,97563,98502,99694,99766,99886,101623,102062,103815,104484,104687,104744,104993,105162,105441,105729,105826,105860,105882,106048,106480,106874,107819,108334,108560,109192,109724,110472,110829,111016,111120,112190,113274,114440,114495,114766,116030,117257,117386,117849,118130,118257,118292],"is_not":false,"summary":null,"term":"GO:0023052"},{"annotations":[99930,101337],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007189"},{"annotations":[101338,114974,116006,106311,105962,93734,108471,108977,105373],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010619"},{"annotations":[65714],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0009785"},{"annotations":[118007,97608,112798,91907],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097720"},{"annotations":[88243,116824,90726,97609,97160,91909],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0019722"},{"annotations":[115925,115586,117662],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061762"},{"annotations":[101631,91773,110428],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000196"},{"annotations":[104999,107907],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007166"},{"annotations":[115028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007267"},{"annotations":[111409,113711,106701,107713,113221,103377,90237,115344,99088],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[108772],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000077"},{"annotations":[92454,115473,116221,116668,109026,94001,116825,113249,113651,106643,113519,100728,89177,98217],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030968"},{"annotations":[116319],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006984"},{"annotations":[96546,106602,109475,87655],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007186"},{"annotations":[94724,102812,98938,109131],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140469"},{"annotations":[87984,91595,89435,115766,90999,92716,90444,95163,100874,71710,93332,107909,95823,112152,114349,87813,116371,89378,104648,96440,89792,77124,87035,72860,114213,110375,78417,87363,70844,93297,116903,76768,117346,76957,111292,105374],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035556"},{"annotations":[92601,89030],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036498"},{"annotations":[105744],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007254"},{"annotations":[99464,57271],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000165"},{"annotations":[105785,113941],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905318"},{"annotations":[92034],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044778"},{"annotations":[115503,106081,90940],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033315"},{"annotations":[115504,88573,113701,106082],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051598"},{"annotations":[101287,116112,105786],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033316"},{"annotations":[88357],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031930"},{"annotations":[115448,100027,89505,93914,100925],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044878"},{"annotations":[98690,113702,93444,91301,106083,110650,115449,115678,101847,108773,79553,77532,117151,93066,113912],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044773"},{"annotations":[116716,93466,106084,115505,98857,108774,102805,107301,111484,93445,116246,100028,88632,116547,98691,90941,92035],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033314"},{"annotations":[88458,101848,115346,101111,108346],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031568"},{"annotations":[90817,109132],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031571"},{"annotations":[95354,94045,115450,97934],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031569"},{"annotations":[98859,117152,88633,93446,91302,100029,106085,88062,90942,116461,113703,108775,100543,89724,111180],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007095"},{"annotations":[101849,100348,94046,95515,106086,115507,88679,90943,111181,115506,101013,88634,89959,88063,98860,107131,111485,92036,98692,116548],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031573"},{"annotations":[113944,101288,105787,116115,113225,114999,109369,90239,98932],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007094"},{"annotations":[115825],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0106072"},{"annotations":[115826,91596,92254,107434,99932],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0110034"},{"annotations":[100487,115573],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0106057"},{"annotations":[98939,107076,103288,95355,117751,106512],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903138"},{"annotations":[88949,101632,102330],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902660"},{"annotations":[106603,87721],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0043409"},{"annotations":[93706],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[98941,117752,94537,95475,116522,91171],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903753"},{"annotations":[106604],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0180040"},{"annotations":[92826],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0090029"},{"annotations":[110816],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0046580"},{"annotations":[104813],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0035024"},{"annotations":[107006,109627,106564,104507,92432,99090,90241,91240,100766,106703,115347,92961,95143,99168,92348],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0031030"},{"annotations":[111163,105365,90748],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:2000639"},{"annotations":[90771],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0032007"},{"annotations":[102496,115574,109135,113418,95602,100941,98378,92832,87537,106864,114022,99072,117665,104601,93679,108725,112601,110408,106617,115929,116486],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1904262"},{"annotations":[115720],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903940"},{"annotations":[100392,109798,87060,101246,105745,93876],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0038066"},{"annotations":[91696,105746,88746,95880,92827,96547],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071507"},{"annotations":[87656],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000750"},{"annotations":[92726,97095,92886,95434,110583],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048015"},{"annotations":[68925,117717,90667,94758,111272,65874,66013,111924],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000160"},{"annotations":[101635,110429],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0050850"},{"annotations":[88950,90281,87599,91926,102331],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903139"},{"annotations":[113226],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[116119],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[116813,108399,108400,108401,94759,108404,111273,108398,117718,108402,108403,111925],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1900745"},{"annotations":[90360,115031,114068,87658,103190],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0062038"},{"annotations":[90671],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0046579"},{"annotations":[93309,87054,89512,101875,109976],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0031031"},{"annotations":[116429,112878,112880,93187,93189,93188,112879],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2000640"},{"annotations":[104602,106038],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0032008"},{"annotations":[108726,112306,93826,97507,88933,109992,95603,106618,87538,117802,87827],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1904263"},{"annotations":[97245,90704,106461],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1904515"},{"annotations":[118220,111918,112493,90648,99669,104828],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0062200"},{"annotations":[110463,104529],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031291"},{"annotations":[91864,79958],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0043408"},{"annotations":[100826],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"},{"annotations":[93707],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090266"},{"annotations":[94538],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1900744"},{"annotations":[115945,69591],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032483"},{"annotations":[112807,89474,103984],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0031029"},{"annotations":[89405],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0023051"},{"annotations":[93560,92399,104603,107314,117236,114924],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903432"},{"annotations":[99035],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007266"},{"annotations":[87056,93923,105853,114916,106565,88754,106610,100437],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031028"},{"annotations":[70392,114783,89247,109564,109644,87371,97125,76798,104594,88728,92216,87564,90697,91648,108880,88742,94442,89439,107869,93350,90476,87419,106300,105286,112679,94917,65146,74723,64928,95830,102419,95891,103746,91253,109538,98037,117451],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007165"},{"annotations":[115032,110818,105847,90364],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032005"},{"annotations":[104651],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090520"},{"annotations":[97325,109313,103458,112009,88501,101599,93388,92147,116431,89163,88778,112261,105311,117669,117877,115840],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032933"},{"annotations":[103448,103791],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031929"},{"annotations":[91598,114368,106126,92719,75054,116573,98062,106151,112468],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0038202"},{"annotations":[102217,98879,101249,106152,108037,117818],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0038203"}]},"cv_name":"biological_process","definition":"The entirety of a process in which information is transmitted within a biological system. This process begins with an active signal and ends when a cellular response has been triggered.","definition_xrefs":["GOC:mtg_signal","GOC:signaling","GOC:mtg_signaling_feb11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process","termid":"GO:0050789"}],"gene_count":404,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00028":null,"SJAG_00071":null,"SJAG_00078":null,"SJAG_00082":null,"SJAG_00092":null,"SJAG_00100":null,"SJAG_00114":null,"SJAG_00117":null,"SJAG_00142":null,"SJAG_00143":null,"SJAG_00167":null,"SJAG_00169":null,"SJAG_00209":null,"SJAG_00210":null,"SJAG_00214":null,"SJAG_00216":null,"SJAG_00226":null,"SJAG_00229":null,"SJAG_00236":null,"SJAG_00244":null,"SJAG_00256":null,"SJAG_00266":null,"SJAG_00289":null,"SJAG_00293":null,"SJAG_00296":null,"SJAG_00317":null,"SJAG_00318":null,"SJAG_00321":null,"SJAG_00327":null,"SJAG_00329":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00340":null,"SJAG_00356":null,"SJAG_00364":null,"SJAG_00369":null,"SJAG_00402":null,"SJAG_00424":null,"SJAG_00429":null,"SJAG_00439":null,"SJAG_00457":null,"SJAG_00472":null,"SJAG_00486":null,"SJAG_00509":null,"SJAG_00514":null,"SJAG_00526":null,"SJAG_00530":null,"SJAG_00534":null,"SJAG_00551":null,"SJAG_00561":null,"SJAG_00574":null,"SJAG_00600":null,"SJAG_00610":null,"SJAG_00623":null,"SJAG_00640":null,"SJAG_00642":null,"SJAG_00649":null,"SJAG_00661":null,"SJAG_00678":null,"SJAG_00681":null,"SJAG_00688":null,"SJAG_00690":null,"SJAG_00704":null,"SJAG_00718":null,"SJAG_00781":null,"SJAG_00790":null,"SJAG_00807":null,"SJAG_00823":null,"SJAG_00824":null,"SJAG_00845":null,"SJAG_00858":null,"SJAG_00875":null,"SJAG_00883":null,"SJAG_00963":null,"SJAG_00975":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_00993":null,"SJAG_00996":null,"SJAG_01000":null,"SJAG_01010":null,"SJAG_01020":null,"SJAG_01032":null,"SJAG_01040":null,"SJAG_01044":null,"SJAG_01047":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01114":null,"SJAG_01118":null,"SJAG_01138":null,"SJAG_01142":null,"SJAG_01146":null,"SJAG_01150":null,"SJAG_01161":null,"SJAG_01181":null,"SJAG_01184":null,"SJAG_01187":null,"SJAG_01188":null,"SJAG_01199":null,"SJAG_01205":null,"SJAG_01210":null,"SJAG_01213":null,"SJAG_01245":null,"SJAG_01253":null,"SJAG_01254":null,"SJAG_01270":null,"SJAG_01286":null,"SJAG_01297":null,"SJAG_01307":null,"SJAG_01311":null,"SJAG_01320":null,"SJAG_01330":null,"SJAG_01345":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01386":null,"SJAG_01401":null,"SJAG_01429":null,"SJAG_01464":null,"SJAG_01509":null,"SJAG_01516":null,"SJAG_01519":null,"SJAG_01585":null,"SJAG_01587":null,"SJAG_01605":null,"SJAG_01632":null,"SJAG_01657":null,"SJAG_01667":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01699":null,"SJAG_01703":null,"SJAG_01708":null,"SJAG_01716":null,"SJAG_01718":null,"SJAG_01754":null,"SJAG_01768":null,"SJAG_01774":null,"SJAG_01787":null,"SJAG_01790":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_01821":null,"SJAG_01825":null,"SJAG_01837":null,"SJAG_01855":null,"SJAG_01873":null,"SJAG_01885":null,"SJAG_01901":null,"SJAG_01906":null,"SJAG_01942":null,"SJAG_01978":null,"SJAG_01983":null,"SJAG_02000":null,"SJAG_02013":null,"SJAG_02022":null,"SJAG_02026":null,"SJAG_02027":null,"SJAG_02058":null,"SJAG_02072":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02135":null,"SJAG_02169":null,"SJAG_02183":null,"SJAG_02203":null,"SJAG_02231":null,"SJAG_02232":null,"SJAG_02233":null,"SJAG_02249":null,"SJAG_02258":null,"SJAG_02266":null,"SJAG_02278":null,"SJAG_02289":null,"SJAG_02311":null,"SJAG_02318":null,"SJAG_02321":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02366":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02389":null,"SJAG_02392":null,"SJAG_02404":null,"SJAG_02424":null,"SJAG_02426":null,"SJAG_02429":null,"SJAG_02433":null,"SJAG_02444":null,"SJAG_02451":null,"SJAG_02468":null,"SJAG_02472":null,"SJAG_02481":null,"SJAG_02486":null,"SJAG_02498":null,"SJAG_02514":null,"SJAG_02520":null,"SJAG_02536":null,"SJAG_02563":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02601":null,"SJAG_02605":null,"SJAG_02682":null,"SJAG_02684":null,"SJAG_02703":null,"SJAG_02712":null,"SJAG_02723":null,"SJAG_02736":null,"SJAG_02760":null,"SJAG_02765":null,"SJAG_02771":null,"SJAG_02785":null,"SJAG_02819":null,"SJAG_02823":null,"SJAG_02838":null,"SJAG_02854":null,"SJAG_02858":null,"SJAG_02860":null,"SJAG_02878":null,"SJAG_02921":null,"SJAG_02923":null,"SJAG_02945":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03067":null,"SJAG_03072":null,"SJAG_03073":null,"SJAG_03081":null,"SJAG_03089":null,"SJAG_03090":null,"SJAG_03126":null,"SJAG_03137":null,"SJAG_03160":null,"SJAG_03185":null,"SJAG_03209":null,"SJAG_03248":null,"SJAG_03263":null,"SJAG_03272":null,"SJAG_03302":null,"SJAG_03309":null,"SJAG_03310":null,"SJAG_03319":null,"SJAG_03327":null,"SJAG_03338":null,"SJAG_03340":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03353":null,"SJAG_03355":null,"SJAG_03361":null,"SJAG_03371":null,"SJAG_03376":null,"SJAG_03384":null,"SJAG_03386":null,"SJAG_03405":null,"SJAG_03421":null,"SJAG_03438":null,"SJAG_03453":null,"SJAG_03482":null,"SJAG_03486":null,"SJAG_03488":null,"SJAG_03501":null,"SJAG_03508":null,"SJAG_03525":null,"SJAG_03529":null,"SJAG_03557":null,"SJAG_03568":null,"SJAG_03591":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03611":null,"SJAG_03623":null,"SJAG_03624":null,"SJAG_03625":null,"SJAG_03631":null,"SJAG_03637":null,"SJAG_03655":null,"SJAG_03678":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03705":null,"SJAG_03709":null,"SJAG_03720":null,"SJAG_03739":null,"SJAG_03748":null,"SJAG_03753":null,"SJAG_03793":null,"SJAG_03799":null,"SJAG_03802":null,"SJAG_03828":null,"SJAG_03841":null,"SJAG_03854":null,"SJAG_03879":null,"SJAG_03887":null,"SJAG_03893":null,"SJAG_03898":null,"SJAG_03903":null,"SJAG_03907":null,"SJAG_03927":null,"SJAG_03928":null,"SJAG_03931":null,"SJAG_03936":null,"SJAG_03940":null,"SJAG_03942":null,"SJAG_03969":null,"SJAG_03987":null,"SJAG_04018":null,"SJAG_04026":null,"SJAG_04052":null,"SJAG_04083":null,"SJAG_04103":null,"SJAG_04118":null,"SJAG_04126":null,"SJAG_04128":null,"SJAG_04140":null,"SJAG_04151":null,"SJAG_04200":null,"SJAG_04206":null,"SJAG_04232":null,"SJAG_04235":null,"SJAG_04249":null,"SJAG_04259":null,"SJAG_04262":null,"SJAG_04268":null,"SJAG_04280":null,"SJAG_04283":null,"SJAG_04287":null,"SJAG_04312":null,"SJAG_04329":null,"SJAG_04332":null,"SJAG_04343":null,"SJAG_04383":null,"SJAG_04384":null,"SJAG_04394":null,"SJAG_04412":null,"SJAG_04426":null,"SJAG_04435":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04460":null,"SJAG_04461":null,"SJAG_04462":null,"SJAG_04464":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04471":null,"SJAG_04486":null,"SJAG_04496":null,"SJAG_04503":null,"SJAG_04507":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04537":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04573":null,"SJAG_04597":null,"SJAG_04638":null,"SJAG_04655":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04671":null,"SJAG_04699":null,"SJAG_04734":null,"SJAG_04761":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04776":null,"SJAG_04777":null,"SJAG_04825":null,"SJAG_04871":null,"SJAG_04873":null,"SJAG_04884":null,"SJAG_04910":null,"SJAG_04920":null,"SJAG_04943":null,"SJAG_04968":null,"SJAG_04980":null,"SJAG_04987":null,"SJAG_04999":null,"SJAG_05000":null,"SJAG_05030":null,"SJAG_05184":null,"SJAG_05286":null,"SJAG_05290":null,"SJAG_05304":null,"SJAG_05330":null,"SJAG_05335":null,"SJAG_05346":null,"SJAG_05373":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_06588":null,"SJAG_06592":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"in_subsets":["bp_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"signaling","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:0023046","GO:0044700"],"synonyms":[{"name":"biological signaling","type":"exact"},{"name":"signaling process","type":"exact"},{"name":"signalling","type":"exact"},{"name":"signalling process","type":"related"},{"name":"single organism signaling","type":"related"}],"termid":"GO:0023052","terms_by_termid":{"GO:0000077":null,"GO:0000160":null,"GO:0000165":null,"GO:0000196":null,"GO:0000750":null,"GO:0006984":null,"GO:0007094":null,"GO:0007095":null,"GO:0007165":null,"GO:0007166":null,"GO:0007186":null,"GO:0007189":null,"GO:0007254":null,"GO:0007266":null,"GO:0007267":null,"GO:0009785":null,"GO:0010619":null,"GO:0019722":null,"GO:0023051":null,"GO:0023052":null,"GO:0030968":null,"GO:0031028":null,"GO:0031029":null,"GO:0031030":null,"GO:0031031":null,"GO:0031291":null,"GO:0031568":null,"GO:0031569":null,"GO:0031571":null,"GO:0031573":null,"GO:0031929":null,"GO:0031930":null,"GO:0032005":null,"GO:0032007":null,"GO:0032008":null,"GO:0032483":null,"GO:0032933":null,"GO:0033314":null,"GO:0033315":null,"GO:0033316":null,"GO:0035024":null,"GO:0035556":null,"GO:0036498":null,"GO:0038066":null,"GO:0038202":null,"GO:0038203":null,"GO:0043408":null,"GO:0043409":null,"GO:0044773":null,"GO:0044778":null,"GO:0044878":null,"GO:0046579":null,"GO:0046580":null,"GO:0048015":null,"GO:0050850":null,"GO:0051598":null,"GO:0061762":null,"GO:0062038":null,"GO:0062200":null,"GO:0071507":null,"GO:0090029":null,"GO:0090266":null,"GO:0090267":null,"GO:0090520":null,"GO:0097720":null,"GO:0106057":null,"GO:0106072":null,"GO:0110034":null,"GO:0140469":null,"GO:0140499":null,"GO:0180040":null,"GO:1900744":null,"GO:1900745":null,"GO:1902426":null,"GO:1902660":null,"GO:1903138":null,"GO:1903139":null,"GO:1903432":null,"GO:1903753":null,"GO:1903940":null,"GO:1904262":null,"GO:1904263":null,"GO:1904515":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:2000639":null,"GO:2000640":null}}


id: PBO:0002904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F1-ATPase alpha subunit","termid":"PBO:0002904"}


id: MONDO:0004775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"iridocyclitis","termid":"MONDO:0004773"}],"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":"lens-induced iridocyclitis","secondary_identifiers":["ICD9:364.23","SCTID:70461003","UMLS:C0339320","DOID:9388","MEDGEN:573082"],"synonyms":[{"name":"lens-induced iridocyclitis","type":"exact"}],"termid":"MONDO:0004775","xrefs":{"Monarch":{"xref_id":"0004775"}}}


id: GO:0048017
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals in which a cell uses an inositol-containing lipid to convert a signal into a response. Inositol lipids include the phosphoinositides (phosphatidylinositol and its phosphorylated derivatives), ceramides containing inositol, and inositol glycolipids.","definition_xrefs":["GOC:bf","GOC:ceb","PMID:16088939"],"gene_count":0,"genotype_count":0,"name":"obsolete inositol lipid-mediated signaling (obsolete GO:0048017)","synonyms":[{"name":"inositol lipid-mediated signal transduction","type":"exact"},{"name":"inositol lipid-mediated signalling","type":"exact"},{"name":"inositol phospholipid-mediated signaling","type":"narrow"}],"termid":"GO:0048017"}


id: PATO:0000744
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000744 balance value (obsolete PATO:0000744)","termid":"PATO:0000744"}


id: MONDO:1012253
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spastic paresis, non-human animal","termid":"MONDO:1011859"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spastic paresis, cattle","secondary_identifiers":["OMIA:000928-9913"],"termid":"MONDO:1012253","xrefs":{"Monarch":{"xref_id":"1012253"}}}


id: PBO:0060855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEK2 pseudogene 3","termid":"PBO:0060855"}


id: MONDO:0014573
data:
  {"annotated_genes":["SJAG_02349"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84972],"is_not":false,"summary":null,"term":"MONDO:0014573"}]},"cv_name":"mondo","definition":"Any Cole-Carpenter syndrome in which the cause of the disease is a mutation in the SEC24D gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Cole-Carpenter syndrome","termid":"MONDO:0016085"},{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02349":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"Cole-Carpenter syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:905199","GARD:16077","UMLS:C4225382","OMIM:616294"],"synonyms":[{"name":"CLCRP2","type":"related"},{"name":"COLE-CARPENTER syndrome 2","type":"related"},{"name":"Cole-Carpenter syndrome 2","type":"exact"},{"name":"Cole-Carpenter syndrome caused by mutation in SEC24D","type":"exact"},{"name":"Cole-Carpenter syndrome type 2","type":"exact"},{"name":"SEC24D Cole-Carpenter syndrome","type":"exact"}],"termid":"MONDO:0014573","terms_by_termid":{"MONDO:0014573":null},"xrefs":{"Monarch":{"xref_id":"0014573"}}}


id: FYPO:0003060
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of reciprocal meiotic recombination at a cis-acting homologous chromosome pairing region such as the sme2 locus is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased meiotic recombination","termid":"FYPO:0000485"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased meiotic recombination at cis-acting homologous chromosome pairing region","synonyms":[{"name":"decreased meiotic recombination at sme2 locus","type":"narrow"},{"name":"reduced meiotic recombination at cis-acting homologous chromosome pairing region","type":"exact"}],"termid":"FYPO:0003060"}


id: FYPO:0004329
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid separation is normal (i.e. indistinguishable from wild type) in regions containing ribosomal DNA (rDNA). Mitotic sister chromatid separation is the process in which sister chromatids are physically detached from each other during mitosis.","definition_xrefs":["PMID:17032733","PomBase:mah","GO:0051306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic sister chromatid separation","termid":"FYPO:0004301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal mitotic rDNA separation","synonyms":[{"name":"normal mitotic chromosome separation at rDNA","type":"exact"},{"name":"normal mitotic rDNA separation during vegetative growth","type":"exact"},{"name":"normal mitotic ribosomal DNA separation","type":"exact"},{"name":"normal mitotic sister chromatid separation at rDNA","type":"exact"},{"name":"normal rDNA separation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0004329"}


id: SO:0000206
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A repetitive element, a few hundred base pairs long, that is dispersed throughout the genome. A common human SINE is the Alu element.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_LTR_retrotransposon","termid":"SO:0000189"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SINE_element","secondary_identifiers":["http://en.wikipedia.org/wiki/Short_interspersed_nuclear_element"],"synonyms":[{"name":"SINE element","type":"exact"},{"name":"Short interspersed element","type":"exact"},{"name":"Short interspersed nuclear element","type":"exact"}],"termid":"SO:0000206"}


id: PBO:0108888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 1","termid":"PBO:0108888"}


id: MONDO:0005829
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute tick-borne arbovirus infection causing meningoencephalomyelitis of sheep.","definition_xrefs":["MESH:D008146"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sheep disease","termid":"MONDO:0024985"},{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"louping ill","secondary_identifiers":["DOID:10250","ICD9:063.1"],"synonyms":[{"name":"Louping ill","type":"exact"}],"termid":"MONDO:0005829","xrefs":{"Monarch":{"xref_id":"0005829"}}}


id: PBO:0056355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule associated protein 9","termid":"PBO:0056355"}


id: PBO:0044664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"doublecortin","termid":"PBO:0044664"}


id: GO:0044736
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transmembrane transfer of a sodium ion by a neuronal, voltage-insensitive channel that opens when an extracellular proton has been bound by the channel complex.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete acid-sensing ion channel activity (obsolete GO:0044736)","secondary_identifiers":["Wikipedia:Acid-sensing_ion_channel"],"synonyms":[{"name":"ASIC activity","type":"exact"}],"termid":"GO:0044736"}


id: GO:0018211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical alteration of a tryptophan residue in a peptide.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-amino acid modification","termid":"GO:0018193"}],"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-tryptophan modification","termid":"GO:0018211"}


id: PBO:0058058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4279","termid":"PBO:0058058"}


id: PBO:0028301
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_phosphatase_activity_during_mitosis","termid":"PBO:0028301"}


id: PBO:0060465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NALF1 intronic transcript 1","termid":"PBO:0060465"}


id: MONDO:0009654
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mucopolysaccharidoses, unclassified types (obsolete MONDO:0009654)","secondary_identifiers":["OMIM:252700","MESH:C562442"],"synonyms":[{"name":"mucopolysaccharidoses, unclassified types","type":"exact"}],"termid":"MONDO:0009654","xrefs":{"Monarch":{"xref_id":"0009654"}}}


id: GO:0080034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in the state or activity of a host cell or organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of the formation of an abnormal mass of cells in the host organism, induced by a symbiont. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:18836040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to symbiont","termid":"GO:0009608"}],"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":"host response to induction by symbiont of tumor, nodule or growth in host","termid":"GO:0080034"}


id: GO:0072173
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a metanephric tubule are generated and organized from an epithelium. A metanephric tubule is an epithelial tube that is part of the metanephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial tube morphogenesis","termid":"GO:0060562"},{"relation_name":"part_of","term_name":"metanephric tubule development","termid":"GO:0072170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric tubule morphogenesis","termid":"GO:0072173"}


id: GO:0051942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of amino acid neurotransmitters into a neuron or glial cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of neurotransmitter uptake","termid":"GO:0051581"},{"relation_name":"is_a","term_name":"regulation of amino acid uptake involved in synaptic transmission","termid":"GO:0051941"},{"relation_name":"is_a","term_name":"negative regulation of amino acid transport","termid":"GO:0051956"},{"relation_name":"negatively_regulates","term_name":"amino acid neurotransmitter reuptake","termid":"GO:0051933"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of amino acid uptake involved in synaptic transmission","synonyms":[{"name":"down regulation of amino acid uptake during transmission of nerve impulse","type":"related"},{"name":"down-regulation of amino acid uptake during transmission of nerve impulse","type":"related"},{"name":"downregulation of amino acid uptake during transmission of nerve impulse","type":"related"},{"name":"inhibition of amino acid uptake during transmission of nerve impulse","type":"related"},{"name":"negative regulation of amino acid neurotransmitter reuptake","type":"exact"},{"name":"negative regulation of amino acid neurotransmitter uptake","type":"exact"},{"name":"negative regulation of amino acid uptake during transmission of nerve impulse","type":"related"}],"termid":"GO:0051942"}


id: GO:0030312
data:
  {"annotated_genes":["SJAG_03824","SJAG_00620","SJAG_04238","SJAG_03483","SJAG_01321","SJAG_01028","SJAG_04720","SJAG_01288","SJAG_04067","SJAG_04771","SJAG_04864","SJAG_02135","SJAG_01970","SJAG_01017","SJAG_04723","SJAG_02093","SJAG_04236","SJAG_02916","SJAG_03204","SJAG_01835","SJAG_00876","SJAG_03057","SJAG_04073","SJAG_00218","SJAG_00784","SJAG_04184","SJAG_03828","SJAG_02478","SJAG_06622","SJAG_02649","SJAG_03295","SJAG_02945","SJAG_00096","SJAG_01975","SJAG_02192","SJAG_01086","SJAG_05285","SJAG_00340","SJAG_00027","SJAG_03903","SJAG_01290","SJAG_02131","SJAG_04327","SJAG_01755","SJAG_02222","SJAG_03013","SJAG_00239","SJAG_06621"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[113523,113810,108530,89757,117227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005619"},{"annotations":[107238],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043188"},{"annotations":[91275],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005631"},{"annotations":[115401,100296,115400,88207,92001,92002,100297],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010339"},{"annotations":[102209,100558,102456,101134,106322,101135,116008,102455],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070263"},{"annotations":[108373,114200,101942,117772,103652,106158,112778,91388,107854,100304,105566,108370,108376,101001,112605,91101,89434,108375,109898,108374,87582,86964,88657,89631,112777,115067,88208,117219,115045,108372,93521,94603,91091,109899,113920,108371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009277"},{"annotations":[87033],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005632"},{"annotations":[87139,87138,115262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031160"}]},"cv_name":"cellular_component","definition":"A structure that lies outside the plasma membrane and surrounds the entire cell or cells. This does not include the periplasmic space.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cell periphery","termid":"GO:0071944"}],"gene_count":48,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00096":null,"SJAG_00218":null,"SJAG_00239":null,"SJAG_00340":null,"SJAG_00620":null,"SJAG_00784":null,"SJAG_00876":null,"SJAG_01017":null,"SJAG_01028":null,"SJAG_01086":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01321":null,"SJAG_01755":null,"SJAG_01835":null,"SJAG_01970":null,"SJAG_01975":null,"SJAG_02093":null,"SJAG_02131":null,"SJAG_02135":null,"SJAG_02192":null,"SJAG_02222":null,"SJAG_02478":null,"SJAG_02649":null,"SJAG_02916":null,"SJAG_02945":null,"SJAG_03013":null,"SJAG_03057":null,"SJAG_03204":null,"SJAG_03295":null,"SJAG_03483":null,"SJAG_03824":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_04067":null,"SJAG_04073":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04327":null,"SJAG_04720":null,"SJAG_04723":null,"SJAG_04771":null,"SJAG_04864":null,"SJAG_05285":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"external encapsulating structure","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0030312","terms_by_termid":{"GO:0005619":null,"GO:0005631":null,"GO:0005632":null,"GO:0009277":null,"GO:0010339":null,"GO:0031160":null,"GO:0043188":null,"GO:0070263":null}}


id: GO:0004960
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a thromboxane (TXA) to initiate a change in cell activity.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostanoid receptor activity","termid":"GO:0004954"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"thromboxane receptor activity","synonyms":[{"name":"TXA receptor activity","type":"exact"}],"termid":"GO:0004960"}


id: PBO:0091496
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monogenic PPCDC","termid":"PBO:0091496"}


id: PATO:0001064
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001064 absolute flux (obsolete PATO:0001064)","termid":"PATO:0001064"}


id: GO:1990696
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of four proteins, loss of which results in Usher Syndrome type 2 (USH2 syndrome), a leading genetic cause of combined hearing and vision loss. This complex is conserved in many species; in mice, it is composed of USH2A, GPR98 (aka ADGRV1), WHRN, and PDZD7.","definition_xrefs":["GOC:krc","PMID:25406310"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"USH2 complex","synonyms":[{"name":"USH2 quaternary protein complex","type":"exact"}],"termid":"GO:1990696"}


id: GO:0052774
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glucosyl-N-acetylglucosamine + H2O = glucosamine + N-acetylglucosamine.","definition_xrefs":["GOC:mengo_curators","PMID:16232910","PMID:16736587","PMID:15136574"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosaminidase activity","termid":"GO:0015929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016798","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"glucosyl-N-acetylglucosamine glucosaminidase activity","termid":"GO:0052774"}


id: PBO:0062189
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 Q member 1 pseudogene","termid":"PBO:0062189"}


id: PATO:0001533
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color pattern inhering in a bearer by virtue of bearer's having two or more hues or degrees of saturation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color pattern","termid":"PATO:0000019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multi-colored","synonyms":[{"name":"variegated","type":"exact"}],"termid":"PATO:0001533"}


id: GO:0070076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a histone by the removal of a methyl group from a lysine residue.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone lysine demethylation (obsolete GO:0070076)","termid":"GO:0070076"}


id: PBO:0069730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1011, pseudogene","termid":"PBO:0069730"}


id: MONDO:1010099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pyruvate kinase deficiency of erythrocyte that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate kinase deficiency of erythrocyte, non-human animal","secondary_identifiers":["OMIA:000844"],"termid":"MONDO:1010099","xrefs":{"Monarch":{"xref_id":"1010099"}}}


id: GO:0160157
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A multi-enzyme complex that catalyzes the oxidative decarboxylation of branched-chain alpha-ketoacids derived from L-leucine, L-isoleucine, and L-valine to branched-chain acyl-CoAs. The complex comprises multiple copies of three enzymes referred to as E1, E2 and E3: branched-chain alpha-ketoacid dehydrogenase (E1, a heterotetramer of two alpha and two beta subunits), dihydrolipoyl transacylase (E2), and dihydrolipoamide dehydrogenase (E3). Additional proteins may also be present.","definition_xrefs":["PMID:3593587","PMID:10464218","PMID:10745006"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-ketoacid dehydrogenase complex","termid":"GO:0045240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"branched-chain alpha-ketoacid dehydrogenase complex","secondary_identifiers":["Wikipedia:Branched-chain_alpha-keto_acid_dehydrogenase_complex"],"synonyms":[{"name":"BCKD complex","type":"exact"},{"name":"BKDH complex","type":"exact"}],"termid":"GO:0160157"}


id: PBO:0078941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon CCT) 8-1","termid":"PBO:0078941"}


id: PBO:0087353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Splicing factor; component of the U4/U6-U5 snRNP complex","termid":"PBO:0087353"}


id: PBO:0091543
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-Amylase Homolog","termid":"PBO:0091543"}


id: GO:0019266
data:
  {"annotated_genes":["SJAG_00714"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111262],"is_not":false,"summary":null,"term":"GO:0019266"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of asparagine from other compounds, including oxaloacetate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxaloacetate metabolic process","termid":"GO:0006107"},{"relation_name":"is_a","term_name":"asparagine biosynthetic process","termid":"GO:0006529"},{"relation_name":"is_a","term_name":"dicarboxylic acid catabolic process","termid":"GO:0043649"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00714":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0044248","GO:0008150"],"is_obsolete":false,"name":"asparagine biosynthetic process from oxaloacetate","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:ASPARAGINE-BIOSYNTHESIS"],"synonyms":[{"name":"asparagine anabolism from oxaloacetate","type":"exact"},{"name":"asparagine formation from oxaloacetate","type":"exact"},{"name":"asparagine synthesis from oxaloacetate","type":"exact"}],"termid":"GO:0019266","terms_by_termid":{"GO:0019266":null}}


id: PBO:0072043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 13","termid":"PBO:0072043"}


id: PBO:0017885
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae FPR1","termid":"PBO:0017885"}


id: PBO:0002938
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Suppressor of Uncontrolled Mitosis","termid":"PBO:0002938"}


id: PBO:0036380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin Aly1 related Aly1","termid":"PBO:0036380"}


id: PBO:0053723
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 937","termid":"PBO:0053723"}


id: PBO:0068471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 48, pseudogene","termid":"PBO:0068471"}


id: PBO:0039784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aquaporin 11","termid":"PBO:0039784"}


id: MOD:00860
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that produces an amino acid residue containing an exogenous sulfur atom.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfur containing modified residue","termid":"MOD:00860"}


id: PBO:0051096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy joining 6","termid":"PBO:0051096"}


id: PBO:0039573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and sterile alpha motif domain containing 1A","termid":"PBO:0039573"}


id: GO:0001086
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to a basal RNA polymerase II transcription factor of the TFIIA class in order to modulate transcription. The transcription factor may or may not also interact selectively with DNA as well.","definition_xrefs":["GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription factor activity, TFIIA-class binding (obsolete GO:0001086)","synonyms":[{"name":"TFIIA-class binding transcription factor activity","type":"exact"}],"termid":"GO:0001086"}


id: PBO:0079974
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP9Y pseudogene 12","termid":"PBO:0079974"}


id: GO:0030269
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-methyl-5,6,7,8-tetrahydromethanopterin + coenzyme M + 2 Na+(in) = 5,6,7,8-tetrahydromethanopterin + methyl-coenzyme M + 2 Na+(out). 2-(methylthio)ethanesulfonate is also known as methyl-CoM.","definition_xrefs":["RHEA:53492"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-methyltransferase activity","termid":"GO:0008172"},{"relation_name":"is_a","term_name":"sodium ion transmembrane transporter activity","termid":"GO:0015081"},{"relation_name":"is_a","term_name":"5-methyl-5,6,7,8-tetrahydromethanopterin-dependent methyltransferase activity","termid":"GO:0042086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016741","GO:0005215","GO:0016740","GO:0022857"],"is_obsolete":false,"name":"tetrahydromethanopterin S-methyltransferase activity","secondary_identifiers":["KEGG_REACTION:R04347","MetaCyc:2.1.1.86-RXN","GO:0018709","EC:7.2.1.4","UM-BBD_reactionID:r0355"],"synonyms":[{"name":"5-methyl-5,6,7,8-tetrahydromethanopterin:2-mercaptoethanesulfonate 2-methyltransferase activity","type":"related"},{"name":"N(5)-methyltetrahydromethanopterin--coenzyme M methyltransferase activity","type":"related"},{"name":"N5-methyltetrahydromethanopterin--coenzyme M methyltransferase activity","type":"related"},{"name":"tetrahydromethanopterin methyltransferase activity","type":"related"}],"termid":"GO:0030269"}


id: PR:P0CT36
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- Tf2-3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P0CT36"],"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":"transposon Tf2-3 polyprotein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2E1P3.03c","synonyms":[{"name":"Spom972h-Tf2-3","type":"exact"},{"name":"retrotransposable element Tf2 155 kDa protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P0CT36"}


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


id: PBO:0027531
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_ribonuclease_activity","termid":"PBO:0027531"}


id: PBO:0055126
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 2545","termid":"PBO:0055126"}


id: PBO:0085019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nicotinamide riboside kinase; catalyzes the phosphorylation of nicotinamide riboside and nicotinic acid riboside in salvage pathways for NAD+ biosynthesis","termid":"PBO:0085019"}


id: PBO:0066596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ras homolog family member Q","termid":"PBO:0066596"}


id: PBO:0040661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bardet-Biedl syndrome 7","termid":"PBO:0040661"}


id: MOD:00313
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-palmitoleyl-L-cysteine.","definition_xrefs":["OMSSA:187","RESID:AA0308","PubMed:8294460","Unimod:431#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"S-palmitoleylated residue","termid":"MOD:02002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"},{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905","MOD:01155"],"is_obsolete":false,"name":"S-palmitoleyl-L-cysteine","synonyms":[{"name":"(R)-2-amino-3-((Z)-9-hexadecenoylsulfanyl)propanoic acid","type":"exact"},{"name":"Palmitoleyl","type":"related"},{"name":"S-palmitoleyl-L-cysteine","type":"exact"},{"name":"S-palmitoleylated L-cysteine","type":"exact"},{"name":"SPamD1Cys","type":"exact"},{"name":"cis-9-hexadecenoate cysteine thioester","type":"exact"},{"name":"mod187","type":"exact"},{"name":"palmitoleyl","type":"related"}],"termid":"MOD:00313"}


id: GO:0033991
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: 1,5-anhydro-D-fructose = 2-hydroxy-2-(hydroxymethyl)-2H-pyran-3(6H)-one + H2O; (1a) 1,5-anhydro-D-fructose = 1,5-anhydro-4-deoxy-D-glycero-hex-3-en-2-ulose + H2O and (1b) 1,5-anhydro-4-deoxy-D-glycero-hex-3-en-2-ulose = 2-hydroxy-2-(hydroxymethyl)-2H-pyran-3(6H)-one.","definition_xrefs":["EC:4.2.1.110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"aldos-2-ulose dehydratase activity","secondary_identifiers":["MetaCyc:RXN-14306","RHEA:12100"],"synonyms":[{"name":"1,5-anhydro-D-fructose dehydratase (microthecin-forming) activity","type":"related"},{"name":"1,5-anhydro-D-fructose hydro-lyase (microthecin-forming) activity","type":"related"},{"name":"AUDH","type":"related"},{"name":"pyranosone dehydratase activity","type":"related"}],"termid":"GO:0033991"}


id: GO:0007113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A mitotic cell cycle in which chromosomes are replicated and sister chromatids separate, but spindle formation, nuclear membrane breakdown and nuclear division do not occur, resulting in an increased number of chromosomes in the cell.","definition_xrefs":["GOC:expert_vm","GOC:dos","GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic cell cycle","termid":"GO:0000278"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"endomitotic cell cycle","secondary_identifiers":["Wikipedia:Mitosis#Endomitosis"],"synonyms":[{"name":"endomitosis","type":"related"}],"termid":"GO:0007113"}


id: MONDO:0020582
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm that arises from the uterine ligament.","definition_xrefs":["NCIT:C126493"],"direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system benign neoplasm","termid":"MONDO:0000636"},{"relation_name":"is_a","term_name":"cervical benign neoplasm","termid":"MONDO:0000644"},{"relation_name":"is_a","term_name":"uterine ligament neoplasm","termid":"MONDO:0021629"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign uterine ligament neoplasm","secondary_identifiers":["UMLS:C0865093","MEDGEN:923071"],"synonyms":[{"name":"benign uterine ligament neoplasm","type":"exact"}],"termid":"MONDO:0020582","xrefs":{"Monarch":{"xref_id":"0020582"}}}


id: FYPO:0004070
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 RNA measured in a cell is too low to detect during a cellular response to copper ion starvation. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA absent from cell during vegetative growth","termid":"FYPO:0003161"},{"relation_name":"is_a","term_name":"decreased RNA level during cellular response to copper ion starvation during vegetative growth","termid":"FYPO:0003280"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0006551","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"RNA absent from cell during cellular response to copper ion starvation","synonyms":[{"name":"RNA absent from cell during cellular response to copper ion starvation during mitotic cell cycle","type":"related"},{"name":"RNA absent from cell during cellular response to copper ion starvation during vegetative growth","type":"exact"},{"name":"RNA absent from cell during cellular response to copper starvation","type":"exact"},{"name":"transcripts absent from cell during cellular response to copper ion starvation","type":"exact"},{"name":"undetectable RNA level during cellular response to copper ion starvation","type":"exact"}],"termid":"FYPO:0004070"}


id: GO:0120126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a starvation stimulus, deprivation of copper ion.","definition_xrefs":["GOC:sl","PMID:24024382"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to starvation","termid":"GO:0042594"}],"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 copper ion starvation","termid":"GO:0120126"}


id: GO:1990824
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex that depends on magnesium in order for one or more of its components to remain a part of the complex.","definition_xrefs":["PMID:10220587"],"gene_count":0,"genotype_count":0,"name":"obsolete magnesium-dependent protein complex (obsolete GO:1990824)","termid":"GO:1990824"}


id: GO:0048641
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of skeletal muscle tissue development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of striated muscle tissue development","termid":"GO:0016202"},{"relation_name":"regulates","term_name":"skeletal muscle tissue development","termid":"GO:0007519"}],"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 skeletal muscle tissue development","termid":"GO:0048641"}


id: MONDO:0858987
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive spastic paraplegia type 82 (obsolete MONDO:0858987)","termid":"MONDO:0858987","xrefs":{"Monarch":{"xref_id":"0858987"}}}


id: PBO:0084386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Low affinity methionine permease; similar to Mup1p","termid":"PBO:0084386"}


id: PBO:0050794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxytryptamine receptor 4","termid":"PBO:0050794"}


id: PBO:0054051
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 1393","termid":"PBO:0054051"}


id: PBO:0056450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule affinity regulating kinase 3 pseudogene 2","termid":"PBO:0056450"}


id: RO:0002467
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"is_symbiosis","termid":"RO:0002465"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_mutualism","termid":"RO:0002467"}


id: GO:0001988
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of heart contraction as a result of the baroreceptor response to decreased blood pressure.","definition_xrefs":["ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of heart rate","termid":"GO:0010460"},{"relation_name":"part_of","term_name":"baroreceptor response to decreased systemic arterial blood pressure","termid":"GO:0001982"}],"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 heart rate involved in baroreceptor response to decreased systemic arterial blood pressure","synonyms":[{"name":"activation of heart contraction rate in baroreceptor response to decreased blood pressure","type":"narrow"},{"name":"positive control of heart contraction rate in baroreceptor response to decreased blood pressure","type":"exact"},{"name":"positive regulation of cardiac contraction rate in baroreceptor response to decreased blood pressure","type":"exact"},{"name":"positive regulation of heart contraction rate in baroreceptor response to decreased blood pressure","type":"related"},{"name":"stimulation of heart contraction rate in baroreceptor response to decreased blood pressure","type":"narrow"},{"name":"up regulation of heart contraction rate in baroreceptor response to decreased blood pressure","type":"exact"},{"name":"up-regulation of heart contraction rate in baroreceptor response to decreased blood pressure","type":"exact"},{"name":"upregulation of heart contraction rate in baroreceptor response to decreased blood pressure","type":"exact"}],"termid":"GO:0001988"}


id: PR:P18253
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppi1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P18253"],"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":"peptidyl-prolyl cis-trans isomerase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC28F2.03","synonyms":[{"name":"CPH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Cyclophilin (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PPIase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Rotamase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ppi1","type":"exact"},{"name":"cyclosporin A-binding protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P18253"}


id: GO:0046249
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of alpha-pinene, a monoterpene that may be a significant factor affecting bacterial activities in nature.","definition_xrefs":["PMID:29414896","PMID:10192895","PMID:14736461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-pinene metabolic process","termid":"GO:0018867"},{"relation_name":"is_a","term_name":"pinene catabolic process","termid":"GO:0033074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"alpha-pinene catabolic process","synonyms":[{"name":"alpha-pinene breakdown","type":"exact"},{"name":"alpha-pinene catabolism","type":"exact"},{"name":"alpha-pinene degradation","type":"exact"}],"termid":"GO:0046249"}


id: PBO:0070297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY1 pseudogene 3","termid":"PBO:0070297"}


id: PBO:0075070
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 119","termid":"PBO:0075070"}


id: PBO:0039938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AT-rich interaction domain 1B","termid":"PBO:0039938"}


id: PBO:0063550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"penta-EF-hand domain containing 1","termid":"PBO:0063550"}


id: PBO:0089761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific family with conserved tryptophan","termid":"PBO:0089761"}


id: PBO:0043119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic iron-sulfur assembly component 3","termid":"PBO:0043119"}


id: MONDO:0003424
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm composed of large cells with abundant eosinophilic granular cytoplasm. Representative examples include oncocytic adenomas of the thyroid gland, parathyroid gland, and pituitary gland.","definition_xrefs":["NCIT:C3759"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"benign endocrine neoplasm","termid":"MONDO:0000627"},{"relation_name":"is_a","term_name":"adenoma","termid":"MONDO:0004972"},{"relation_name":"is_a","term_name":"oncocytic neoplasm","termid":"MONDO:0010795"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oncocytic adenoma","secondary_identifiers":["MEDGEN:307150","UMLS:C1510502","DOID:5389","EFO:1001079","ICDO:8290/0"],"synonyms":[{"name":"follicular adenoma, oxyphilic cell","type":"exact"},{"name":"oncocytic adenoma","type":"exact"},{"name":"oncocytoma","type":"exact"},{"name":"oxyphilic adenoma","type":"exact"}],"termid":"MONDO:0003424","xrefs":{"Monarch":{"xref_id":"0003424"}}}


id: MONDO:0000409
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic finding indicating inflammation of the fetal sac membranes. It is characterized by neutrophilic infiltration of the amnion and chorion.","definition_xrefs":["NCIT:C26720"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"},{"relation_name":"is_a","term_name":"disorder of extraembryonic membrane","termid":"MONDO:0045013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chorioamnionitis","secondary_identifiers":["DOID:0050697","MEDGEN:3056","MESH:D002821","UMLS:C0008495","SCTID:11612004"],"synonyms":[{"name":"fetal membrane inflammation","type":"exact"},{"name":"foetal membrane inflammation","type":"exact"},{"name":"inflammation of fetal membrane","type":"exact"},{"name":"inflammation of foetal membrane","type":"exact"},{"name":"intra-amniotic infection","type":"exact"}],"termid":"MONDO:0000409","xrefs":{"Monarch":{"xref_id":"0000409"}}}


id: GO:1902256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of apoptotic process involved in outflow tract morphogenesis.","definition_xrefs":["GOC:TermGenie","GOC:dph","GOC:mtg_apoptosis","PMID:16839542"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process involved in morphogenesis","termid":"GO:1902337"},{"relation_name":"regulates","term_name":"apoptotic process involved in outflow tract morphogenesis","termid":"GO:0003275"}],"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 apoptotic process involved in outflow tract morphogenesis","synonyms":[{"name":"regulation of apoptosis involved in outflow tract morphogenesis","type":"narrow"}],"termid":"GO:1902256"}


id: FYPO:0000341
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 single functional copy of a gene provides sufficient normal function in a diploid cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell phenotype","termid":"FYPO:0003755"}],"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":"haplosufficient","synonyms":[{"name":"haplosufficient during mitotic cell cycle","type":"related"},{"name":"haplosufficient during vegetative growth","type":"exact"}],"termid":"FYPO:0000341"}


id: PBO:0041398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 6 open reading frame 47","termid":"PBO:0041398"}


id: PBO:0043542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coilin pseudogene 1","termid":"PBO:0043542"}


id: PBO:0012001
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"possible horizonal transfer","termid":"PBO:0012001"}


id: PBO:0058148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4444-1","termid":"PBO:0058148"}


id: SO:0001563
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant where copies of a feature (CNV) are either increased or decreased.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_length_variant","termid":"SO:0002160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copy_number_change","synonyms":[{"name":"copy number change","type":"exact"}],"termid":"SO:0001563"}


id: PBO:0083029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Deleted ORF; does not encode a protein; YCR097WA refers to an incorrect annotation of HMRA1 that appeared in the original version of Chromosome III (1996) but was later withdrawn and subsequently removed from SGD","termid":"PBO:0083029"}


id: MONDO:1012254
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spastic syndrome, non-human animal","termid":"MONDO:1011860"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spastic syndrome, cattle","secondary_identifiers":["OMIA:000929-9913"],"termid":"MONDO:1012254","xrefs":{"Monarch":{"xref_id":"1012254"}}}


id: GO:1990636
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A life cycle stage during which the reproductive capacity and fitness of an organism declines.","definition_xrefs":["PMID:27353257","PMID:24914937","PMID:25523082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological phase","termid":"GO:0044848"}],"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 senescence","synonyms":[{"name":"ovarian senescence","type":"narrow"}],"termid":"GO:1990636"}


id: GO:1902066
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell wall pectin metabolic process.","definition_xrefs":["PMID:23453954","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polysaccharide metabolic process","termid":"GO:0032881"},{"relation_name":"regulates","term_name":"cell wall pectin metabolic process","termid":"GO:0052546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of cell wall pectin metabolic process","synonyms":[{"name":"regulation of cell wall pectin metabolism","type":"exact"},{"name":"regulation of cellulose and pectin-containing cell wall pectin metabolic process","type":"exact"},{"name":"regulation of pectin metabolism during cell wall biogenesis","type":"exact"},{"name":"regulation of plant-type cell wall pectin metabolic process","type":"exact"}],"termid":"GO:1902066"}


id: GO:2001055
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mesenchymal cell apoptotic process.","definition_xrefs":["GOC:obol","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of apoptotic process","termid":"GO:0043065"},{"relation_name":"is_a","term_name":"regulation of mesenchymal cell apoptotic process","termid":"GO:2001053"},{"relation_name":"positively_regulates","term_name":"mesenchymal cell apoptotic process","termid":"GO:0097152"}],"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 mesenchymal cell apoptotic process","synonyms":[{"name":"positive regulation of mesenchymal cell apoptosis","type":"narrow"}],"termid":"GO:2001055"}


id: MONDO:0035375
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"post-COVID-19 disorder","termid":"MONDO:0100320"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multisystem inflammatory syndrome in children and adults","secondary_identifiers":["UMLS:C5680268","GARD:22403","MEDGEN:1842571","Orphanet:598363"],"synonyms":[{"name":"MIS-C/A","type":"exact"}],"termid":"MONDO:0035375","xrefs":{"Monarch":{"xref_id":"0035375"}}}


id: MONDO:0020744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by an electrocardiographic finding of intermittent failure of atrial electrical impulse conduction to the ventricles, characterized by a progressively lengthening PR interval prior to the block of an atrial impulse. (CDISC)","definition_xrefs":["NCIT:C62017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"second-degree atrioventricular block","termid":"MONDO:0000467"}],"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":"Mobitz type I atrioventricular block","secondary_identifiers":["MEDGEN:82687","UMLS:C0264907"],"synonyms":[{"name":"AV block second degree Mobitz type I","type":"exact"},{"name":"AV block second degree Möbitz type I","type":"exact"},{"name":"Mobitz I","type":"exact"},{"name":"Mobitz type I","type":"exact"},{"name":"Mobitz type I second degree AV block","type":"exact"},{"name":"Möbitz I","type":"exact"},{"name":"Möbitz type I second degree AV block","type":"exact"},{"name":"Wenckebach block","type":"exact"},{"name":"second degree atrioventricular block Mobitz type I","type":"exact"},{"name":"second degree atrioventricular block Möbitz type I","type":"exact"},{"name":"type 1 2nd degree AV block","type":"exact"},{"name":"type 1 second degree AV block","type":"exact"},{"name":"type 1 second degree atrioventricular block","type":"exact"}],"termid":"MONDO:0020744","xrefs":{"Monarch":{"xref_id":"0020744"}}}


id: PBO:0090383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-type ATPase P5 type","termid":"PBO:0090383"}


id: GO:0035219
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Progression of the prothoracic disc over time, from its initial formation through to its metamorphosis to form the adult humerous and anterior spiracle.","definition_xrefs":["ISBN:0879694238","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc development","termid":"GO:0007444"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"prothoracic disc development","termid":"GO:0035219"}


id: PBO:0089174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L21/aconitate hydratase, fusion protein","termid":"PBO:0089174"}


id: PBO:0004293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rad23 homolog Rhp23","termid":"PBO:0004293"}


id: PR:O94716
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fta4 gene.","definition_xrefs":["UniProtKB:O94716","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":"kinetochore protein fta4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1393.04","synonyms":[{"name":"Spom972h-fta4","type":"exact"},{"name":"sim4 complex subunit fta4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"sim4-mal2-associated protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94716"}


id: GO:0090733
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A extracellular matrix complex involved in cell adhesion and cell migration. Typically homotrimeric or homohexameric. In mammals, four complexes exist: Tenascin-C, Tenascin-N (also known as Tenascin-W), Tenascin-X and Tenascin-R.","definition_xrefs":["GOC:bhm","PMID:11731446","PMID:12845616","PMID:17909022","PMID:23658023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein complex involved in cell-matrix adhesion","termid":"GO:0098637"},{"relation_name":"part_of","term_name":"collagen-containing extracellular matrix","termid":"GO:0062023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"tenascin complex","synonyms":[{"name":"Tenascin-C","type":"narrow"},{"name":"Tenascin-N","type":"narrow"},{"name":"Tenascin-R","type":"narrow"},{"name":"Tenascin-W","type":"narrow"},{"name":"Tenascin-X","type":"narrow"}],"termid":"GO:0090733"}


id: GO:0046639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of alpha-beta T cell differentiation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell differentiation","termid":"GO:0045581"},{"relation_name":"is_a","term_name":"negative regulation of alpha-beta T cell activation","termid":"GO:0046636"},{"relation_name":"is_a","term_name":"regulation of alpha-beta T cell differentiation","termid":"GO:0046637"},{"relation_name":"negatively_regulates","term_name":"alpha-beta T cell differentiation","termid":"GO:0046632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of alpha-beta T cell differentiation","synonyms":[{"name":"down regulation of alpha-beta T cell differentiation","type":"exact"},{"name":"down-regulation of alpha-beta T cell differentiation","type":"exact"},{"name":"downregulation of alpha-beta T cell differentiation","type":"exact"},{"name":"inhibition of alpha-beta T cell differentiation","type":"narrow"},{"name":"negative regulation of alpha-beta T cell development","type":"related"},{"name":"negative regulation of alpha-beta T lymphocyte differentiation","type":"exact"},{"name":"negative regulation of alpha-beta T-cell differentiation","type":"exact"},{"name":"negative regulation of alpha-beta T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0046639"}


id: PBO:0029546
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_vegetative_cell_with_normal_cell_size","termid":"PBO:0029546"}


id: PBO:0080380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS11 divergent transcript","termid":"PBO:0080380"}


id: PBO:0026842
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_swollen,_elongated_pear-shaped_cell","termid":"PBO:0026842"}


id: MONDO:0040964
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete superimposed infection (obsolete MONDO:0040964)","secondary_identifiers":["SCTID:193198003"],"synonyms":[{"name":"superadded infection","type":"related"},{"name":"superimposed infection","type":"exact"},{"name":"suprainfection","type":"related"}],"termid":"MONDO:0040964","xrefs":{"Monarch":{"xref_id":"0040964"}}}


id: MONDO:0008149
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An osteogenesis imperfecta found in a single South African family.","definition_xrefs":["DOID:0110335","PMID:7241530"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta type 1","termid":"MONDO:0008146"}],"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":"osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures","secondary_identifiers":["OMIM:166230","MEDGEN:331579","GARD:15100","MESH:C563487","UMLS:C1833748"],"synonyms":[{"name":"osteogenesis imperfecta with opalescent teeth, blue sclerae and WORMIAN bones, but without fractures","type":"related"}],"termid":"MONDO:0008149","xrefs":{"Monarch":{"xref_id":"0008149"}}}


id: GO:0031717
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a cannabinoid receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"cannabinoid receptor binding","synonyms":[{"name":"cannabinoid receptor ligand","type":"narrow"}],"termid":"GO:0031717"}


id: PBO:0060102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 3","termid":"PBO:0060102"}


id: FYPO:0006336
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 nucleation of microtubules from one or more microtubule organizing centers (MTOCs) occurs to a lesser extent than normal during mitosis.","definition_xrefs":["PMID:8834801","PomBase:mah","GO:0051418"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased microtubule nucleation during vegetative growth","termid":"FYPO:0006335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000054","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased mitotic microtubule nucleation","synonyms":[{"name":"decreased microtubule nucleation by microtubule organizing center during mitosis","type":"exact"},{"name":"decreased microtubule nucleation during M phase of mitotic cell cycle","type":"related"},{"name":"decreased microtubule nucleation during mitosis","type":"exact"},{"name":"decreased mitotic microtubule nucleation during vegetative growth","type":"exact"},{"name":"reduced mitotic microtubule nucleation","type":"exact"}],"termid":"FYPO:0006336"}


id: GO:0046258
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 2,4,6-trinitrotoluene, 1-methyl-2,4,6-trinitrobenzene, a highly explosive pale yellow crystalline solid, in the absence of oxygen.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anaerobic 2,4,6-trinitrotoluene metabolic process","termid":"GO:0018975"},{"relation_name":"is_a","term_name":"2,4,6-trinitrotoluene catabolic process","termid":"GO:0046256"}],"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":"anaerobic 2,4,6-trinitrotoluene catabolic process","synonyms":[{"name":"anaerobic 2,4,6-trinitrotoluene breakdown","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene catabolism","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene degradation","type":"exact"}],"termid":"GO:0046258"}


id: PBO:0062101
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 B member 1","termid":"PBO:0062101"}


id: MONDO:0013639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"narcolepsy","termid":"MONDO:0021107"},{"relation_name":"is_a","term_name":"narcolepsy, susceptibility to","termid":"MONDO:0100049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"narcolepsy 6, susceptibility to","secondary_identifiers":["UMLS:C3280204","MEDGEN:481834","OMIM:614223"],"synonyms":[{"name":"NRCLP6","type":"exact"},{"name":"narcolepsy 6","type":"related"},{"name":"narcolepsy 6, susceptibility to","type":"exact"}],"termid":"MONDO:0013639","xrefs":{"Monarch":{"xref_id":"0013639"}}}


id: PBO:0084035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI-anchored cell surface glycoprotein (flocculin); required for pseudohyphal and invasive growth, flocculation, and biofilm formation; major determinant of colony morphology; QTL that controls chronological life span; carries intragenic tandem repeats that are expanded in different strains; required for formation of fibrous interconnections between cells; role in co-flocculation with other yeast species; cleaved and shed from cells, contributing to their surface properties","termid":"PBO:0084035"}


id: PBO:0047671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"filaggrin","termid":"PBO:0047671"}


id: PBO:0045248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJC27 antisense RNA 1","termid":"PBO:0045248"}


id: GO:0032335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of activin from a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hormone secretion","termid":"GO:0046883"},{"relation_name":"regulates","term_name":"activin secretion","termid":"GO:0032333"}],"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"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of activin secretion","termid":"GO:0032335"}


id: GO:0050207
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction:1-(1,2-saturated alkyl)-2-acyl-sn-glycero-3-phosphoethanolamine + 2 Fe(II)-[cytochrome b5] + 2 H+ + O2 = 1-O-(1Z-alkenyl)-2-acyl-sn-glycero-3-phosphoethanolamine + 2 Fe(III)-[cytochrome b5] + 2 H2O.","definition_xrefs":["RHEA:22956"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water","termid":"GO:0016717"},{"relation_name":"is_a","term_name":"dioxygenase activity","termid":"GO:0051213"}],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"plasmanylethanolamine desaturase activity","secondary_identifiers":["EC:1.14.19.77","MetaCyc:RXN-17732"],"synonyms":[{"name":"2-acyl-1-alkyl-sn-glycero-3-phosphoethanolamine desaturase activity","type":"related"},{"name":"alkylacylglycero-phosphorylethanolamine dehydrogenase activity","type":"related"},{"name":"alkylacylglycerophosphoethanolamine desaturase activity","type":"related"},{"name":"plasmenylethanolamine desaturase activity","type":"exact"}],"termid":"GO:0050207"}


id: MONDO:1011218
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Coloboma that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coloboma, non-human animal","termid":"MONDO:1010319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coloboma, cattle","secondary_identifiers":["OMIA:000219-9913"],"termid":"MONDO:1011218","xrefs":{"Monarch":{"xref_id":"1011218"}}}


id: PBO:0077572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 277, pseudogene","termid":"PBO:0077572"}


id: PBO:0087953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translation termination and ribosome biogenesis factor; ATP binding cassette protein that cosediments with polysomes and is required for biogenesis of the small ribosomal subunit; Asn/Gln-rich rich region supports [NU+] prion formation and susceptibility to [PSI+] prion induction","termid":"PBO:0087953"}


id: PBO:0041221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1GALT1 pseudogene 1","termid":"PBO:0041221"}


id: MONDO:0000486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A focal dystonia that is characterized as dystonia that affects the muscles of the head, face, and neck.","definition_xrefs":["DOID:0050845"],"direct_ancestors":[{"relation_name":"is_a","term_name":"focal dystonia","termid":"MONDO:0000477"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"craniofacial dystonia","secondary_identifiers":["MONDO:0022885","UMLS:C4023011","MEDGEN:868612"],"synonyms":[{"name":"cranio-facial dystonia","type":"exact"}],"termid":"MONDO:0000486","xrefs":{"Monarch":{"xref_id":"0000486"}}}


id: GO:0004322
data:
  {"annotated_genes":["SJAG_03862","SJAG_04677"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91964,113322],"is_not":false,"summary":null,"term":"GO:0004322"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 4 Fe2+ + 4 H+ + O2 = 4 Fe3+ + 2 H2O.","definition_xrefs":["RHEA:11148"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on metal ions, oxygen as acceptor","termid":"GO:0016724"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03862":null,"SJAG_04677":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"ferroxidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-1562604","Reactome:R-HSA-5621402","Reactome:R-HSA-917891","MetaCyc:RXN0-1483","Reactome:R-HSA-1562603","Reactome:R-HSA-1562626","EC:1.16.3.1","Reactome:R-HSA-5691107","Reactome:R-HSA-917933"],"synonyms":[{"name":"Fe(II):oxygen oxidoreductase activity","type":"related"},{"name":"HEPH","type":"narrow"},{"name":"caeruloplasmin","type":"narrow"},{"name":"ceruloplasmin","type":"narrow"},{"name":"ferro:O2 oxidoreductase activity","type":"related"},{"name":"ferroxidase I","type":"related"},{"name":"ferroxidase, iron II:oxygen oxidoreductase activity","type":"related"},{"name":"hephaestin","type":"narrow"},{"name":"iron(II): oxygen oxidoreductase activity","type":"related"},{"name":"multicopper ferroxidase iron transport mediator activity","type":"narrow"}],"termid":"GO:0004322","terms_by_termid":{"GO:0004322":null}}


id: MONDO:0010192
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of Waardenburg syndrome type 4 (Waardenburg-Shah syndrome) caused by mutations in EDNRB.","direct_ancestors":[{"relation_name":"is_a","term_name":"Waardenburg-Shah syndrome","termid":"MONDO:0019518"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0000426"],"is_obsolete":false,"name":"Waardenburg syndrome type 4A","secondary_identifiers":["DOID:0110953","OMIM:277580","GARD:15245","UMLS:C1848519","MEDGEN:341244"],"synonyms":[{"name":"EDNRB Waardenburg syndrome","type":"exact"},{"name":"Shah-Waardenburg syndrome","type":"related"},{"name":"WS4A","type":"exact"},{"name":"Waardenburg syndrome caused by mutation in EDNRB","type":"exact"},{"name":"Waardenburg syndrome type 4A","type":"exact"},{"name":"Waardenburg syndrome type IVA","type":"exact"},{"name":"Waardenburg syndrome with Hirschsprung disease type 4A","type":"exact"},{"name":"Waardenburg syndrome with Hirschsprung disease, type 4A","type":"related"},{"name":"Waardenburg syndrome, type 4A","type":"related"},{"name":"Waardenburg-Shah syndrome","type":"related"},{"name":"Ws4","type":"related"}],"termid":"MONDO:0010192","xrefs":{"Monarch":{"xref_id":"0010192"}}}


id: PBO:0116290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Highly variable glycoprotein localized to cell wall via GPI anchor; serine/threonine rich and highly similar to HPF1 haze-protective mannoprotein; necessary and sufficient for haze-positive phenotype in brewing strains which correlates with an expansion in the N-terminal serine-rich region; transcript is induced in both high and low pH environments","termid":"PBO:0116290"}


id: PBO:0039575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and sterile alpha motif domain containing 3","termid":"PBO:0039575"}


id: FYPO:0002590
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 any tRNA processing intermediates with 3' extensions measured in the mitochondria is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered tRNA or precursor level","termid":"FYPO:0005999"},{"relation_name":"is_a","term_name":"increased ncRNA level during vegetative growth","termid":"FYPO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased level of mitochondrial tRNA processing intermediates with 3' extensions","synonyms":[{"name":"increased accumulation of mitochondrial tRNA processing intermediates with 3' extensions","type":"related"},{"name":"increased level of mitochondrial tRNA processing intermediates with 3' extensions during mitotic cell cycle","type":"related"},{"name":"increased level of mitochondrial tRNA processing intermediates with 3' extensions during vegetative growth","type":"exact"}],"termid":"FYPO:0002590"}


id: GO:1904985
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of quinolinate biosynthetic process.","definition_xrefs":["GOC:bf","GOC:PARL","GOC:TermGenie","PMID:12140278","PMID:19843166","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of quinolinate biosynthetic process","termid":"GO:1904984"},{"relation_name":"negatively_regulates","term_name":"quinolinate biosynthetic process","termid":"GO:0019805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"negative regulation of quinolinate biosynthetic process","synonyms":[{"name":"down regulation of quinolinate anabolism","type":"exact"},{"name":"down regulation of quinolinate biosynthesis","type":"exact"},{"name":"down regulation of quinolinate biosynthetic process","type":"exact"},{"name":"down regulation of quinolinate formation","type":"exact"},{"name":"down regulation of quinolinate synthesis","type":"exact"},{"name":"down-regulation of quinolinate anabolism","type":"exact"},{"name":"down-regulation of quinolinate biosynthesis","type":"exact"},{"name":"down-regulation of quinolinate biosynthetic process","type":"exact"},{"name":"down-regulation of quinolinate formation","type":"exact"},{"name":"down-regulation of quinolinate synthesis","type":"exact"},{"name":"downregulation of quinolinate anabolism","type":"exact"},{"name":"downregulation of quinolinate biosynthesis","type":"exact"},{"name":"downregulation of quinolinate biosynthetic process","type":"exact"},{"name":"downregulation of quinolinate formation","type":"exact"},{"name":"downregulation of quinolinate synthesis","type":"exact"},{"name":"inhibition of quinolinate anabolism","type":"narrow"},{"name":"inhibition of quinolinate biosynthesis","type":"narrow"},{"name":"inhibition of quinolinate biosynthetic process","type":"narrow"},{"name":"inhibition of quinolinate formation","type":"narrow"},{"name":"inhibition of quinolinate synthesis","type":"narrow"},{"name":"negative regulation of quinolinate anabolism","type":"exact"},{"name":"negative regulation of quinolinate biosynthesis","type":"exact"},{"name":"negative regulation of quinolinate formation","type":"exact"},{"name":"negative regulation of quinolinate synthesis","type":"exact"}],"termid":"GO:1904985"}


id: FYPO:0002066
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell has no septum, is elongated, and is inviable.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated aseptate vegetative cell","termid":"FYPO:0000950"},{"relation_name":"is_a","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"},{"relation_name":"is_a","term_name":"inviable aseptate vegetative cell","termid":"FYPO:0003931"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0000631","FYPO:0000005","FYPO:0001320","FYPO:0000002","FYPO:0000004","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"inviable elongated aseptate cell","synonyms":[{"name":"inviable elongated aseptate cell during mitotic cell cycle","type":"related"},{"name":"inviable elongated aseptate cell during vegetative growth","type":"exact"},{"name":"inviable long aseptate cell","type":"exact"},{"name":"lethal; elongated aseptate cell","type":"exact"}],"termid":"FYPO:0002066"}


id: MONDO:0004362
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete placenta disease (obsolete MONDO:0004362)","termid":"MONDO:0004362","xrefs":{"Monarch":{"xref_id":"0004362"}}}


id: PBO:0027863
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K56_acetylation","termid":"PBO:0027863"}


id: PBO:0068135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 442","termid":"PBO:0068135"}


id: GO:0044067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or temporarily subverts the host intercellular junction. Intercellular junction include tight junctions and adherens junctions.","definition_xrefs":["PMID:16102958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated disruption of host cellular anatomical structure","termid":"GO:0052008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host cell-cell junction","synonyms":[{"name":"disruption of host cell-cell junction","type":"broad"},{"name":"modification by symbiont of host cell-cell junction","type":"exact"},{"name":"modification by symbiont of host intercellular junctions","type":"exact"},{"name":"modification of host cell-cell junction","type":"related"},{"name":"modification of host intercellular junctions by symbiont","type":"exact"},{"name":"symbiont-mediated disruption of host cell-cell junction","type":"related"}],"termid":"GO:0044067"}


id: MONDO:0001573
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Friedreich ataxia (obsolete MONDO:0001573)","termid":"MONDO:0001573","xrefs":{"Monarch":{"xref_id":"0001573"}}}


id: GO:0050622
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycine + 2 A = HCN + CO2 + 2 AH2.","definition_xrefs":["RHEA:15821"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"glycine dehydrogenase (cyanide-forming) activity","secondary_identifiers":["MetaCyc:1.4.99.5-RXN","EC:1.4.99.5"],"synonyms":[{"name":"HCN synthase activity","type":"related"},{"name":"glycine:acceptor oxidoreductase (hydrogen-cyanide-forming)","type":"related"},{"name":"hydrogen cyanide synthase activity","type":"related"}],"termid":"GO:0050622"}


id: MONDO:1012178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myoclonus epilepsy of Lafora, non-human animal","termid":"MONDO:1011627"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myoclonus epilepsy of Lafora, dog","secondary_identifiers":["OMIA:000690-9615"],"termid":"MONDO:1012178","xrefs":{"Monarch":{"xref_id":"1012178"}}}


id: GO:0008890
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + glycine = L-2-amino-3-oxobutanoate + CoA.","definition_xrefs":["EC:2.3.1.29","RHEA:20736"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-acetyltransferase activity","termid":"GO:0016453"}],"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:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"glycine C-acetyltransferase activity","secondary_identifiers":["KEGG_REACTION:R00371","MetaCyc:AKBLIG-RXN"],"synonyms":[{"name":"glycine acetyltransferase activity","type":"related"}],"termid":"GO:0008890"}


id: PBO:0078546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 37","termid":"PBO:0078546"}


id: PBO:0046391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EP400 pseudogene 1","termid":"PBO:0046391"}


id: PBO:0029582
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_threonine_phosphorylation_at_Thr-Pro_site","termid":"PBO:0029582"}


id: PBO:0089529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial tRNA wobble uridine modification GTPase Mss1","termid":"PBO:0089529"}


id: PBO:0043147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 15","termid":"PBO:0043147"}


id: MOD:00920
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that modifies an L-valine residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by amino acid modified","termid":"MOD:01157"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified L-valine residue","synonyms":[{"name":"ModVal","type":"exact"}],"termid":"MOD:00920"}


id: MONDO:0016635
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete thrombotic disorder due to a platelet anomaly (obsolete MONDO:0016635)","secondary_identifiers":["Orphanet:248368"],"termid":"MONDO:0016635","xrefs":{"Monarch":{"xref_id":"0016635"}}}


id: MONDO:0000326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lissencephaly (obsolete MONDO:0000326)","termid":"MONDO:0000326","xrefs":{"Monarch":{"xref_id":"0000326"}}}


id: PBO:0027223
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cytoplasmic_microtubules_absent_from_cell","termid":"PBO:0027223"}


id: GO:0033578
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of a carbohydrate or carbohydrate derivative unit to a protein amino acid in any compartment of the Golgi apparatus.","definition_xrefs":["GOC:mah","GOC:pr","PMID:12042244"],"gene_count":0,"genotype_count":0,"name":"obsolete protein glycosylation in Golgi (obsolete GO:0033578)","synonyms":[{"name":"protein amino acid glycosylation in Golgi","type":"exact"},{"name":"terminal glycosylation","type":"narrow"}],"termid":"GO:0033578"}


id: GO:0004488
data:
  {"annotated_genes":["SJAG_00106","SJAG_01126","SJAG_04156"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104267,107810,111864],"is_not":false,"summary":null,"term":"GO:0004488"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,10-methylenetetrahydrofolate + NADP+ = 5,10-methenyltetrahydrofolate + NADPH.","definition_xrefs":["EC:1.5.1.5","RHEA:22812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylenetetrahydrofolate dehydrogenase [NAD(P)+] activity","termid":"GO:0004486"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00106":null,"SJAG_01126":null,"SJAG_04156":null},"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:0003674","GO:0016491"],"is_obsolete":false,"name":"methylenetetrahydrofolate dehydrogenase (NADP+) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R01220","MetaCyc:METHYLENETHFDEHYDROG-NADP-RXN"],"synonyms":[{"name":"5,10-methylenetetrahydrofolate:NADP oxidoreductase activity","type":"related"},{"name":"5,10-methylenetetrahydrofolate:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0004488","terms_by_termid":{"GO:0004488":null}}


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


id: PBO:0056125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LysM domain containing 2","termid":"PBO:0056125"}


id: MONDO:0017172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis type 6","termid":"MONDO:0009661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0002561","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"mucopolysaccharidosis type 6, slowly progressing","secondary_identifiers":["Orphanet:276223","GARD:21047","MEDGEN:1842694","SCTID:67854007","UMLS:C5679780"],"synonyms":[{"name":"MPS6, slowly progressing","type":"exact"},{"name":"MPSVI, slowly progressing","type":"exact"},{"name":"arylsulfatase B deficiency, slowly progressing","type":"exact"},{"name":"mucopolysaccharidosis type VI, slowly progressing","type":"exact"}],"termid":"MONDO:0017172","xrefs":{"Monarch":{"xref_id":"0017172"}}}


id: PBO:0083176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps TEL07R","termid":"PBO:0083176"}


id: MONDO:0009194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare progressive disease that begins as a primary Epstein-Barr virus (EBV) infection. In this type of infection, the body makes too many lymphocytes (lymphoproliferative disease) for a period of more than 6 months duration. Lymphocytes are a type of white blood cell. They are an importantpart ofthe immune system because they help fight off diseases and protect the body from infection byproducing antibodies against viruses or bacteria and regulating immune responses. In CAEBV there are many antibodies againstEBV in the blood.Most people (about 95% of adults) get infected with EBV at some point in their lives, and never have any health problems.However, EBV can cause infectiousmononucleosis and other illnesses, and has a role in various autoimmune diseases and some types of cancer. While most infections occurring during childhood do not cause any symptoms,EBV infection in adolescents or young adults can often result in mononucleosis.After an EBV infection, the virus becomes latent (inactive) in the body, and, in some cases, the virus may reactivate. This does not always cause symptoms, but people with weakened immune systems are more likely to develop symptoms if EBV reactivates.In rare cases, people infected with EBV develop chronic active EBV virus infection(CAEBV) without apparent immunodeficiency. Most cases of CAEBV have been reported from Japan. These patientshave some of the complications found in otherwise-healthy patients with acute EBV infection, but unlike healthy patients, these complications persist and progress. Symptoms of CAEBV most often include fever, liverdysfunction, an enlarged spleen (splenomegaly), swollen lymph nodes (lymphadenopathy), and low numbers of platelets (thrombocytopenia) as well as high EBV-DNA load in the blood. Other features that appear in more than 10% of patients include enlarged liver (hepatomegaly), anemia, hypersensitivity to mosquito bites, rash, oral ulcers, hemophagocytic syndrome, coronary artery aneurysms, liver failure, lymphoma, and interstitial pneumonia. While the cause is yet unknown, researchers have identified defects in T cells or natural killer (NK) cells activity which results in a decreased defense against the EBV in people with CAEBV.It is important to note that the fatigue and malaise from acute infectious mononucleosis (IM)varies from mild symptoms lasting only a few weeks, to more severe symptoms of fatigue that can persist for several months, or even up to a year or more in up to 10% of patients (which may be considered a less severe form of chronicEBV infection). The persistence of fatigue that is seen in some patients after acute IM would lead some people to believe that EBV may also cause cases of chronic fatigue syndrome (CFS). However, no convincing link has been found between EBV and CFS.Hematopoietic stemcell transplantation has shown promise in the treatment of CAEBV.","definition_xrefs":["GARD:0009534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"viral infectious disease","termid":"MONDO:0005108"},{"relation_name":"is_a","term_name":"post-viral disorder","termid":"MONDO:0021674"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunodeficiency 32B","secondary_identifiers":["Orphanet:2566","OMIM:226990","DOID:0111985","NANDO:2200808","OMIM:614894","UMLS:C4016741","GARD:9534","MEDGEN:865178"],"synonyms":[{"name":"CAEBV infection","type":"related"},{"name":"CAEBV syndrome","type":"exact"},{"name":"CEBV","type":"related"},{"name":"Epstein-Barr VIRUS, susceptibility to chronic infection by","type":"related"},{"name":"IMD32B","type":"exact"},{"name":"IRF8 deficiency, autosomal recessive","type":"exact"},{"name":"chronic EBV infection syndrome","type":"exact"},{"name":"chronic Epstein-Barr virus infection syndrome","type":"exact"},{"name":"chronic active Epstein-Barr disease","type":"related"},{"name":"chronic active Epstein-Barr virus infection","type":"related"},{"name":"immunodeficiency 32B","type":"exact"},{"name":"immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive","type":"exact"},{"name":"immunodeficiency 32B, monocyte, Dendritic cell, and natural Killer cell deficiency, autosomal recessive","type":"exact"},{"name":"monocyte and dendritic cell deficiency, autosomal recessive","type":"exact"}],"termid":"MONDO:0009194","xrefs":{"Monarch":{"xref_id":"0009194"}}}


id: PBO:0067762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 62","termid":"PBO:0067762"}


id: GO:0030353
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Interacts with the fibroblast growth factor receptor to reduce the action of another ligand, the agonist.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroblast growth factor receptor binding","termid":"GO:0005104"},{"relation_name":"is_a","term_name":"receptor antagonist activity","termid":"GO:0048019"}],"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:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0140678","GO:0005488","GO:0003674","GO:0005515","GO:0098772"],"is_obsolete":false,"name":"fibroblast growth factor receptor antagonist activity","synonyms":[{"name":"FGF receptor antagonist activity","type":"exact"},{"name":"FGFR antagonist activity","type":"exact"}],"termid":"GO:0030353"}


id: PBO:0051560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 11 receptor subunit alpha","termid":"PBO:0051560"}


id: MONDO:0017660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic parkinsonian disorder (obsolete MONDO:0017660)","secondary_identifiers":["Orphanet:307052"],"synonyms":[{"name":"rare genetic hypokinetic movement disorder","type":"exact"}],"termid":"MONDO:0017660","xrefs":{"Monarch":{"xref_id":"0017660"}}}


id: MONDO:0014923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any peeling skin syndrome in which the cause of the disease is a mutation in the SERPINB8 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exfoliative ichthyosis","termid":"MONDO:0017339"},{"relation_name":"is_a","term_name":"peeling skin syndrome","termid":"MONDO:0019347"}],"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":"peeling skin syndrome 5","secondary_identifiers":["UMLS:C4310710","GARD:18427","DOID:0070524","MEDGEN:934677","OMIM:617115"],"synonyms":[{"name":"PSS5","type":"exact"},{"name":"SERPINB8 peeling skin syndrome","type":"exact"},{"name":"peeling skin syndrome 5","type":"exact"},{"name":"peeling skin syndrome 5; PSS5","type":"exact"},{"name":"peeling skin syndrome caused by mutation in SERPINB8","type":"exact"},{"name":"peeling skin syndrome type 5","type":"exact"}],"termid":"MONDO:0014923","xrefs":{"Monarch":{"xref_id":"0014923"}}}


id: MONDO:0000854
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Stickler syndrome (obsolete MONDO:0000854)","termid":"MONDO:0000854","xrefs":{"Monarch":{"xref_id":"0000854"}}}


id: FYPO:0005506
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 one or more mitochondrial transport mRNAs measured in a cell is higher than normal (i.e. higher than observed in wild-type cells). Mitochondrial transport mRNAs are transcribed from genes whose products are involved in transport to or from the mitochondrion.","definition_xrefs":["PomBase:mah","PMID:23236291"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of transport gene mRNA during vegetative growth","termid":"FYPO:0004490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0006551","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased level of mitochondrial transport gene mRNA during vegetative growth","synonyms":[{"name":"increased level of mitochondrial transport gene RNA during vegetative growth","type":"exact"},{"name":"increased level of mitochondrial transport gene mRNA during mitotic cell cycle","type":"related"},{"name":"increased level of mitochondrial transport gene transcripts during vegetative growth","type":"exact"},{"name":"increased mitochondrial transport gene mRNA accumulation during vegetative growth","type":"related"}],"termid":"FYPO:0005506"}


id: PBO:0045438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dpy-19 like C-mannosyltransferase 3","termid":"PBO:0045438"}


id: PBO:0086520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved across S. cerevisiae strains; partially overlaps dubious ORF YFL015W-A; YFL015C is not an essential gene","termid":"PBO:0086520"}


id: RO:0002005
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"innervated_by","termid":"RO:0002005"}


id: GO:1904149
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of microglial cell mediated cytotoxicity.","definition_xrefs":["GOC:BHF","GOC:TermGenie","GO_REF:0000058","PMID:19100238","GOC:nc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte mediated cytotoxicity","termid":"GO:0001910"},{"relation_name":"is_a","term_name":"regulation of myeloid leukocyte mediated immunity","termid":"GO:0002886"},{"relation_name":"regulates","term_name":"microglial cell mediated cytotoxicity","termid":"GO:0090634"}],"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 microglial cell mediated cytotoxicity","termid":"GO:1904149"}


id: PBO:0087392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S/T kinase and catalytic subunit of DDK (Dbf4-dependent kinase); required for origin firing and replication initiation; phosphorylates MCM subunits and Cdc45 to drive assembly of the pre-IC and the CMG helicase; maintains Cse4p at kinetochores through phosphorylation to regulate chromosome segregation, regulates pre-meiotic replication, meiotic DSB formation, monopolar attachment of homologs during MI through monopolin recruitment and middle meiotic gene expression; HsCDC7 and DBF4 complement","termid":"PBO:0087392"}


id: PBO:0047169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 197 Y-linked member 2","termid":"PBO:0047169"}


id: PBO:0088907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane borate efflux transmembrane transporter Bor1","termid":"PBO:0088907"}


id: GO:2000244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of FtsZ-dependent cytokinesis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokinesis","termid":"GO:0032465"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"FtsZ-dependent cytokinesis","termid":"GO:0043093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of FtsZ-dependent cytokinesis","synonyms":[{"name":"regulation of prokaryote-type cytokinesis","type":"related"},{"name":"regulation of prokaryotic fission","type":"related"}],"termid":"GO:2000244"}


id: GO:0044269
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycerol ethers, any anhydride formed between two organic hydroxy compounds, one of which is glycerol.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerol ether metabolic process","termid":"GO:0006662"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"glycerol ether catabolic process","synonyms":[{"name":"glycerol ether breakdown","type":"exact"},{"name":"glycerol ether catabolism","type":"exact"},{"name":"glycerol ether degradation","type":"exact"}],"termid":"GO:0044269"}


id: PBO:0056248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"male germ cell associated kinase","termid":"PBO:0056248"}


id: PBO:0003592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar sorting protein Vps68 (predicted)","termid":"PBO:0003592"}


id: GO:0099119
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: S-adenosyl-L-methionine + 3-demethylubiquinol-8 = S-adenosyl-L-homocysteine + ubiquinol-8.","definition_xrefs":["GOC:ic"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-demethylubiquinol-8 3-O-methyltransferase activity (obsolete GO:0099119)","termid":"GO:0099119"}


id: PBO:0062458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 136 pseudogene","termid":"PBO:0062458"}


id: PBO:0067601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 764, pseudogene","termid":"PBO:0067601"}


id: MONDO:1010849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lysosomal storage disease in which there is a buildup of glycogen due to a lack of the enzyme alpha-glucosidase in Japanese quail.","definition_xrefs":["OMIA:000419-93934"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"glycogen storage disease, non-human animal","termid":"MONDO:1011419"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogen storage disease II, Japanese quail","termid":"MONDO:1010849","xrefs":{"Monarch":{"xref_id":"1010849"}}}


id: PBO:0036387
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by Rhodotorula minuta DPS1","termid":"PBO:0036387"}


id: PBO:0080918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YWHAQ pseudogene 7","termid":"PBO:0080918"}


id: PBO:0091254
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is not functionally complemented by S. cerevisiae CHS3","termid":"PBO:0091254"}


id: PATO:0002298
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A cellular motility which is higher relative to the normal or average.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"cellular motility","termid":"PATO:0001488"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased cellular motility","termid":"PATO:0002298"}


id: PBO:0003203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-acylglycerol-3-phosphate acyltransferase (predicted)","termid":"PBO:0003203"}


id: PBO:0078014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 4","termid":"PBO:0078014"}


id: MONDO:0007166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary ataxia","termid":"MONDO:0100309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxia with fasciculations","secondary_identifiers":["MEDGEN:400052","MESH:C566246","UMLS:C1862440","OMIM:108700"],"synonyms":[{"name":"ataxia with fasciculations","type":"exact"}],"termid":"MONDO:0007166","xrefs":{"Monarch":{"xref_id":"0007166"}}}


id: MONDO:0017808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"duplication of the pituitary gland","secondary_identifiers":["UMLS:C4755258","GARD:21381","MEDGEN:1663161","Orphanet:314621"],"synonyms":[{"name":"DPG-plus syndrome","type":"exact"},{"name":"Duplication of the pituitary gland-plus syndrome","type":"exact"},{"name":"hypophyseal duplication","type":"exact"}],"termid":"MONDO:0017808","xrefs":{"Monarch":{"xref_id":"0017808"}}}


id: FYPO:0001222
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which a cell contains two nuclei.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multinucleate vegetative cell","termid":"FYPO:0000061"}],"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:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"binucleate vegetative cell","synonyms":[{"name":"binucleate cells during vegetative growth","type":"exact"},{"name":"binucleate during vegetative growth","type":"exact"},{"name":"binucleate vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001222"}


id: GO:0003849
data:
  {"annotated_genes":["SJAG_03580","SJAG_00224"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94095,100747],"is_not":false,"summary":null,"term":"GO:0003849"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-erythrose 4-phosphate + H2O + phosphoenolpyruvate = 7-phospho-2-dehydro-3-deoxy-D-arabino-heptonate + phosphate.","definition_xrefs":["RHEA:14717","EC:2.5.1.54"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00224":null,"SJAG_03580":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016765"}],"interesting_parent_ids":["GO:0016765","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"3-deoxy-7-phosphoheptulonate synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R01826","MetaCyc:DAHPSYN-RXN"],"synonyms":[{"name":"2-dehydro-3-deoxy-phosphoheptonate aldolase activity","type":"related"},{"name":"2-dehydro-3-deoxyphosphoheptonate aldolase activity","type":"exact"},{"name":"2-keto-3-deoxy-D-arabino-heptonic acid 7-phosphate synthetase activity","type":"related"},{"name":"3-deoxy-D-arabino-2-heptulosonic acid 7-phosphate synthetase activity","type":"related"},{"name":"3-deoxy-D-arabino-heptolosonate-7-phosphate synthetase activity","type":"related"},{"name":"3-deoxy-D-arabino-heptulosonate 7-phosphate synthetase activity","type":"related"},{"name":"7-phospho-2-dehydro-3-deoxy-D-arabino-heptonate","type":"related"},{"name":"7-phospho-2-dehydro-3-deoxy-D-arabino-heptonate D-erythrose-4-phosphate lyase (pyruvate-phosphorylating) activity","type":"related"},{"name":"7-phospho-2-keto-3-deoxy-D-arabino-heptonate D-erythrose-4-phosphate lyase (pyruvate-phosphorylating) activity","type":"related"},{"name":"D-erythrose-4-phosphate-lyase (pyruvate-phosphorylating) activity","type":"related"},{"name":"D-erythrose-4-phosphate-lyase activity","type":"related"},{"name":"DAH7-P synthase activity","type":"related"},{"name":"DAHP synthase activity","type":"related"},{"name":"DHAP synthase activity","type":"related"},{"name":"DS-Co activity","type":"related"},{"name":"DS-Mn activity","type":"related"},{"name":"KDPH synthase activity","type":"related"},{"name":"KDPH synthetase activity","type":"related"},{"name":"deoxy-D-arabino-heptulosonate-7-phosphate synthetase activity","type":"related"},{"name":"phospho-2-dehydro-3-deoxyheptonate aldolase activity","type":"related"},{"name":"phospho-2-keto-3-deoxyheptanoate aldolase activity","type":"related"},{"name":"phospho-2-keto-3-deoxyheptonate aldolase activity","type":"related"},{"name":"phospho-2-keto-3-deoxyheptonic aldolase activity","type":"related"},{"name":"phospho-2-oxo-3-deoxyheptonate aldolase activity","type":"related"},{"name":"phosphoenolpyruvate:D-erythrose-4-phosphate C-(1-carboxyvinyl)transferase (phosphate-hydrolysing, 2-carboxy-2-oxoethyl-forming)","type":"related"}],"termid":"GO:0003849","terms_by_termid":{"GO:0003849":null}}


id: PBO:0108691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ArfGEF Spo7","termid":"PBO:0108691"}


id: GO:1990451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a disturbance in the homeostasis of organismal or cellular pH (with pH < 7). pH is a measure of the acidity or basicity of an aqueous solution.","definition_xrefs":["GOC:go_curators","GOC:BHF","GOC:rl","PMID:10615049"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to chemical stress","termid":"GO:0062197"},{"relation_name":"is_a","term_name":"cellular response to acidic pH","termid":"GO:0071468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular stress response to acidic pH","synonyms":[{"name":"cellular stress response to acidity","type":"broad"}],"termid":"GO:1990451"}


id: PBO:0030269
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-swollen_elongated_cell","termid":"PBO:0030269"}


id: MONDO:0009998
data:
  {"annotated_genes":["SJAG_02879"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84738],"is_not":false,"summary":null,"term":"MONDO:0009998"}]},"cv_name":"mondo","definition":"Richieri Costa-Pereira syndrome is characterized by short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs), and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent low set ears and a highly arched palate were also observed. Transmission is autosomal recessive.","definition_xrefs":["Orphanet:3102"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02879":null},"genotype_count":0,"is_obsolete":false,"name":"Richieri Costa-Pereira syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:268305","UMLS:C1849348","SCTID:723998001","icd11.foundation:107084177","MEDGEN:336581","MESH:C535677","GARD:4718"],"synonyms":[{"name":"ROBIN sequence with cleft mandible and limb anomalies","type":"related"},{"name":"Richieri Costa Pereira syndrome","type":"related"},{"name":"Richieri Costa-Pereira syndrome","type":"exact"},{"name":"Richieri-Costa and Pereira form of acrofacial dysostosis","type":"related"},{"name":"Richieri-Costa-Pereira syndrome","type":"related"},{"name":"short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot","type":"related"},{"name":"short stature-Pierre Robin sequence-cleft mandible-hand anomalies clubfoot syndrome","type":"exact"},{"name":"short stature-Pierre Robin syndrome-cleft mandible-hand anomalies clubfoot syndrome","type":"exact"}],"termid":"MONDO:0009998","terms_by_termid":{"MONDO:0009998":null},"xrefs":{"Monarch":{"xref_id":"0009998"}}}


id: MONDO:0027772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of lung adenocarcinoma characterized by the presence of mucin pools containing islands of well differentiated adenocarcinoma cells.","definition_xrefs":["NCIT:C45512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"},{"relation_name":"is_a","term_name":"lung adenocarcinoma","termid":"MONDO:0005061"}],"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":"lung colloid adenocarcinoma","secondary_identifiers":["DOID:0080304","UMLS:C1708776","DOID:0080303","MEDGEN:313370"],"synonyms":[{"name":"lung colloid adenocarcinoma","type":"exact"},{"name":"lung mucinous cystadenocarcinoma","type":"exact"},{"name":"lung mucinous cystic tumor of borderline malignancy","type":"exact"},{"name":"lung mucinous cystic tumour of borderline malignancy","type":"exact"},{"name":"mucinous lung adenocarcinoma","type":"related"}],"termid":"MONDO:0027772","xrefs":{"Monarch":{"xref_id":"0027772"}}}


id: GO:0001647
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with cytokinin and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["GOC:dph","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"},{"relation_name":"is_a","term_name":"cytokinin receptor activity","termid":"GO:0009884"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"G protein-coupled cytokinin receptor activity","synonyms":[{"name":"G protein coupled cytokinin receptor activity","type":"exact"},{"name":"G-protein coupled cytokinin receptor activity","type":"exact"},{"name":"cytokinin receptor activity, G-protein coupled","type":"exact"}],"termid":"GO:0001647"}


id: GO:0097165
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A dense aggregation in the nucleus composed of proteins and RNAs that appear when the cell is under stress.","definition_xrefs":["PMID:10359787","GOC:ans","PMID:12865437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoprotein granule","termid":"GO:0035770"},{"relation_name":"part_of","term_name":"nucleus","termid":"GO:0005634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"nuclear stress granule","termid":"GO:0097165"}


id: PBO:0066089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RASA2 intronic transcript 1","termid":"PBO:0066089"}


id: GO:0061511
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The centrosome organization process by which a centriole increases in length as part of the process of replication.","definition_xrefs":["GOC:dph","PMID:21576394"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"part_of","term_name":"centriole replication","termid":"GO:0007099"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0000226"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0007010","GO:0000226","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"centriole elongation","termid":"GO:0061511"}


id: MONDO:0019851
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of primary ovarian failure that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary endocrine growth disease","termid":"MONDO:0015514"},{"relation_name":"excluded_subClassOf","term_name":"obsolete rare endocrine growth disease (obsolete MONDO:0019590)","termid":"MONDO:0019590"},{"relation_name":"is_a","term_name":"primary ovarian failure","termid":"MONDO:0005387"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acquired primary ovarian failure","secondary_identifiers":["SCTID:717954003","MEDGEN:929209","GARD:19293","Orphanet:95709","UMLS:C4303540"],"synonyms":[{"name":"acquired premature ovarian failure","type":"related"},{"name":"acquired primary ovarian failure","type":"exact"}],"termid":"MONDO:0019851","xrefs":{"Monarch":{"xref_id":"0019851"}}}


id: GO:0046219
data:
  {"annotated_genes":["SJAG_02505","SJAG_03167","SJAG_05007","SJAG_01455"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114105,103873,91085,102985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000162"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of indolalkylamines, indole or indole derivatives containing a primary, secondary, or tertiary amine group.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"indolalkylamine metabolic process","termid":"GO:0006586"},{"relation_name":"is_a","term_name":"biogenic amine biosynthetic process","termid":"GO:0042401"},{"relation_name":"is_a","term_name":"indole-containing compound biosynthetic process","termid":"GO:0042435"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01455":null,"SJAG_02505":null,"SJAG_03167":null,"SJAG_05007":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"indolalkylamine biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-209931"],"synonyms":[{"name":"indolalkylamine anabolism","type":"exact"},{"name":"indolalkylamine biosynthesis","type":"exact"},{"name":"indolalkylamine formation","type":"exact"},{"name":"indolalkylamine synthesis","type":"exact"}],"termid":"GO:0046219","terms_by_termid":{"GO:0000162":null}}


id: PBO:0010218
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene merge, SPNCRNA.502 was a subsequence of SPNCRNA.1228","termid":"PBO:0010218"}


id: MOD:00009
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that removes a residue, or inserts or replaces a residue with a natural, standard or nonstandard, encoded residue.","definition_xrefs":["RESID:AA0000","PubMed:6692818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by amino acid modified","termid":"MOD:01157"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"natural residue","synonyms":[{"name":"Res","type":"exact"},{"name":"alpha-amino acid","type":"exact"}],"termid":"MOD:00009"}


id: GO:0047424
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 H2O + methylenediurea = CO2 + 2 NH3 + N-hydroxymethylurea.","definition_xrefs":["RHEA:15929","MetaCyc:3.5.3.21-RXN","EC:3.5.3.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines","termid":"GO:0016813"},{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"methylenediurea deaminase activity","synonyms":[{"name":"methylenediurea aminohydrolase activity","type":"related"},{"name":"methylenediurease activity","type":"related"}],"termid":"GO:0047424"}


id: GO:0006948
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of syncytia-forming cell-cell fusion, caused by a virus.","definition_xrefs":["ISBN:0781718325"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by virus of host cell-cell fusion (obsolete GO:0006948)","secondary_identifiers":["Reactome:R-HSA-9733458"],"synonyms":[{"name":"induction by virus of cell-cell fusion in host","type":"exact"},{"name":"viral-induced cell-cell fusion","type":"exact"},{"name":"viral-induced host cell-cell fusion","type":"exact"},{"name":"viral-induced membrane fusion","type":"narrow"}],"termid":"GO:0006948"}


id: PATO:0002000
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of physical entities inhering in a bearer by virtue of the bearer's lacking a physical part as specified by the additional entity.","definition_xrefs":["PATOC:CJM"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lacks parts or has fewer parts of type","termid":"PATO:0001999"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lacks all parts of type","secondary_identifiers":["PATO:0001557","OBO_REL:lacks_part"],"synonyms":[{"name":"lacks all physical parts of type","type":"exact"}],"termid":"PATO:0002000"}


id: GO:0009007
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + DNA adenine = S-adenosyl-L-homocysteine + DNA 6-methylaminopurine.","definition_xrefs":["EC:2.1.1.72"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"},{"relation_name":"is_a","term_name":"DNA-methyltransferase activity","termid":"GO:0009008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016741","GO:0003674","GO:0140097","GO:0016740"],"is_obsolete":false,"name":"site-specific DNA-methyltransferase (adenine-specific) activity","secondary_identifiers":["MetaCyc:2.1.1.72-RXN","RHEA:15197"],"synonyms":[{"name":"DNA adenine methylase","type":"broad"},{"name":"EcoRI methylase","type":"narrow"},{"name":"N-6 adenine-specific DNA methylase activity","type":"related"},{"name":"modification methylase activity","type":"related"},{"name":"restriction-modification system activity","type":"related"}],"termid":"GO:0009007"}


id: PR:O14120
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mvp1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14120"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin mvp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A11.06","synonyms":[{"name":"Spom972h-mvp1","type":"exact"}],"termid":"PR:O14120"}


id: PBO:0058372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4744","termid":"PBO:0058372"}


id: PBO:0079774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP-glucose 6-dehydrogenase","termid":"PBO:0079774"}


id: FYPO:0002134
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which an interaction between a protein and RNA is decreased. One of the relevant gene products may be encoded by the mutated gene, or both the RNA and protein may be encoded by genes other than the mutated one.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-RNA interaction","termid":"FYPO:0002132"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0002131"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002131","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"decreased protein-RNA interaction","synonyms":[{"name":"decreased RNA binding","type":"exact"},{"name":"decreased RNA-protein interaction","type":"exact"},{"name":"reduced RNA binding","type":"exact"}],"termid":"FYPO:0002134"}


id: PBO:0028919
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transcription","termid":"PBO:0028919"}


id: MONDO:1012383
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"trapped neutrophil syndrome, non-human animal","termid":"MONDO:1011700"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trapped neutrophil syndrome, dog","secondary_identifiers":["OMIA:001428-9615"],"termid":"MONDO:1012383","xrefs":{"Monarch":{"xref_id":"1012383"}}}


id: PBO:0002564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sm snRNP core protein Smd1","termid":"PBO:0002564"}


id: MONDO:0100213
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An X-linked multiple congenital anomaly disorder with variable severity. The classic triad, which defines IFAP, is ichthyosis follicularis, atrichia, and photophobia. Some patients have additional features, including mental retardation, brain anomalies, Hirschsprung disease, corneal opacifications, kidney dysplasia, cryptorchidism, cleft palate, and skeletal malformations, particularly of the vertebrae, which constitutes BRESHECK syndrome.","definition_xrefs":["OMIM:308205"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete malformation syndrome with skin/mucosae involvement (obsolete MONDO:0015331)","termid":"MONDO:0015331"},{"relation_name":"excluded_subClassOf","term_name":"X-linked ichthyosis syndrome","termid":"MONDO:0017269"},{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary alopecia (obsolete MONDO:0021034)","termid":"MONDO:0021034"},{"relation_name":"is_a","term_name":"X-linked recessive disease","termid":"MONDO:0020605"},{"relation_name":"is_a","term_name":"IFAP syndrome","termid":"MONDO:0100212"}],"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":"IFAP syndrome 1, with or without BRESHECK syndrome","secondary_identifiers":["MESH:C536085","GARD:15297","DOID:0111821","NANDO:2200999","UMLS:C5399971","MEDGEN:1746744"],"synonyms":[{"name":"IFAP syndrome with or without BRESHECK syndrome","type":"exact"},{"name":"IFAP syndrome with or without BRESHECK syndrome, X-linked recessive","type":"exact"},{"name":"IFAP/BRESHECK syndrome","type":"exact"},{"name":"ichthyosis follicularis atrichia photophobia syndrome","type":"related"},{"name":"ichthyosis follicularis, atrichia, and photophobia with or without brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, Ear/eye anomalies, cleft palate/cryptorchidism, and kidney dysplasia/hypoplasia","type":"exact"},{"name":"ichthyosis follicularis-alopecia-photophobia syndrome","type":"broad"}],"termid":"MONDO:0100213","xrefs":{"Monarch":{"xref_id":"0100213"}}}


id: FYPO:0004226
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which nucleosome binding by a gene product (usually a protein) in a mutant does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein-protein interaction","termid":"FYPO:0000705"},{"relation_name":"is_a","term_name":"abolished chromatin binding","termid":"FYPO:0001093"},{"relation_name":"is_a","term_name":"abnormal nucleosome binding","termid":"FYPO:0004225"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000702"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000702","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"abolished nucleosome binding","synonyms":[{"name":"nucleosome binding abolished","type":"exact"}],"termid":"FYPO:0004226"}


id: MONDO:0003207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete eccrine adenocarcinoma (obsolete MONDO:0003207)","termid":"MONDO:0003207","xrefs":{"Monarch":{"xref_id":"0003207"}}}


id: GO:0035676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an anterior lateral line neuromast hair cell over time, from its formation to the mature structure. A neuromast hair cell is a hair cell that acts as a sensory receptor of the neuromast; it is morphologically polarized as a result of the relative position of the single kinocilium and the clusters of stereocilia on its apical surface. Cell development does not include the steps involved in committing a cell to a specific fate.","definition_xrefs":["ISBN:0125296509","ISBN:0387968377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuromast hair cell development","termid":"GO:0035675"},{"relation_name":"part_of","term_name":"anterior lateral line neuromast hair cell differentiation","termid":"GO:0048903"}],"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":"anterior lateral line neuromast hair cell development","termid":"GO:0035676"}


id: PR:O13651
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An isoleucine--tRNA ligase, cytoplasmic that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11946:SF11","PRO:DNx","OMA:SCHPO02832"],"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":"isoleucine--tRNA ligase, cytoplasmic (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC8D2.06","secondary_identifiers":["UniProtKB:O13651"],"synonyms":[{"name":"IleRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-IARS","type":"exact"},{"name":"isoleucyl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13651"}


id: PBO:0003186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal biogenesis factor 11 (predicted)","termid":"PBO:0003186"}


id: PBO:0047630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FIGNL1 interacting regulator of recombination and mitosis","termid":"PBO:0047630"}


id: PBO:0059432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane spanning 4-domains A3","termid":"PBO:0059432"}


id: PR:O14065
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC962.01 gene.","definition_xrefs":["UniProtKB:O14065","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 C962.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC962.01","synonyms":[{"name":"Spom972h-SPCC962.01","type":"exact"}],"termid":"PR:O14065"}


id: PBO:0027701
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_nucleolar_chromatin_organization_resulting_in_peripheral_chromatin_distribution","termid":"PBO:0027701"}


id: FYPO:0002088
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 more exocytic vesicles than normal near the division septum while the cell is undergoing septum assembly.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exocytic vesicles present in increased numbers","termid":"FYPO:0002086"}],"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":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"exocytic vesicles present in increased numbers at septum during septum assembly","synonyms":[{"name":"accumulation of exocytic vesicles at division septum during septum assembly","type":"related"},{"name":"additional exocytic vesicles present at division septum during septum assembly","type":"exact"},{"name":"exocytic vesicles present in greater numbers at division septum during septum assembly","type":"exact"},{"name":"exocytic vesicles present in increased numbers at division septum during mitotic telophase","type":"related"},{"name":"exocytic vesicles present in increased numbers at division septum during septum assembly during mitotic cell cycle","type":"related"},{"name":"exocytic vesicles present in increased numbers at division septum during septum assembly during vegetative growth","type":"exact"},{"name":"exocytic vesicles present in increased numbers at septum during septation","type":"broad"},{"name":"exocytotic vesicles present in increased numbers at division septum during septum assembly","type":"exact"},{"name":"extra exocytic vesicles at division septum during septum assembly","type":"exact"},{"name":"post-Golgi secretory vesicles present in increased numbers at division septum during septum assembly","type":"related"}],"termid":"FYPO:0002088"}


id: PBO:0012601
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frataxin","termid":"PBO:0012601"}


id: PBO:0111462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA (m1A) methyltransferase complex catalytic subunit Trm61","termid":"PBO:0111462"}


id: PBO:0011099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper membrane transporter, meiotic Mfc1","termid":"PBO:0011099"}


id: GO:0102480
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + flucytosine + H2O = 5-fluorouracil + ammonium.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 5-fluorocytosine deaminase activity (obsolete GO:0102480)","termid":"GO:0102480"}


id: GO:0004082
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-phospho-D-glyceroyl phosphate = 2,3-bisphospho-D-glycerate.","definition_xrefs":["EC:5.4.2.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular phosphotransferase activity","termid":"GO:0016868"}],"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:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"bisphosphoglycerate mutase activity","secondary_identifiers":["MetaCyc:BISPHOSPHOGLYCERATE-MUTASE-RXN","RHEA:17765","Reactome:R-HSA-6798335"],"synonyms":[{"name":"2,3-bisphosphoglycerate mutase activity","type":"related"},{"name":"2,3-bisphosphoglycerate synthase activity","type":"related"},{"name":"2,3-diphosphoglycerate mutase activity","type":"related"},{"name":"2,3-diphosphoglycerate synthase activity","type":"related"},{"name":"2,3-diphosphoglyceromutase activity","type":"related"},{"name":"3-phospho-D-glycerate 1,2-phosphomutase activity","type":"related"},{"name":"BPGM activity","type":"related"},{"name":"DPGM","type":"related"},{"name":"biphosphoglycerate synthase activity","type":"related"},{"name":"bisphosphoglycerate synthase activity","type":"related"},{"name":"bisphosphoglyceromutase","type":"broad"},{"name":"diphosphoglycerate mutase activity","type":"related"},{"name":"diphosphoglyceric mutase activity","type":"related"},{"name":"diphosphoglyceromutase activity","type":"related"},{"name":"glycerate phosphomutase activity","type":"related"}],"termid":"GO:0004082"}


id: PR:Q8TFH5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAPB17E12.09 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q8TFH5"],"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":"meiotically up-regulated protein PB17E12.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB17E12.09","synonyms":[{"name":"Spom972h-SPAPB17E12.09","type":"exact"}],"termid":"PR:Q8TFH5"}


id: MONDO:0000334
data:
  {"annotated_genes":["SJAG_03689"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86239],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007681"}]},"cv_name":"mondo","definition":"Nodular goiter characterized by more than one discrete tissue mass.","definition_xrefs":["NCIT:C131438"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"nodular goiter","termid":"MONDO:0006869"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03689":null},"genotype_count":0,"is_obsolete":false,"name":"multinodular goiter","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:87431","OMIMPS:138800","SCTID:237570007","UMLS:C0342208","DOID:0050489"],"synonyms":[{"name":"goiter, multinodular","type":"exact"}],"termid":"MONDO:0000334","terms_by_termid":{"MONDO:0007681":null},"xrefs":{"Monarch":{"xref_id":"0000334"}}}


id: PBO:0086522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved across S. cerevisiae strains; partially overlaps the dubious gene YOR072W-A; diploid deletion strains are methotrexate, paraquat and wortmannin sensitive","termid":"PBO:0086522"}


id: PBO:0083850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Exosome non-catalytic core component; involved in 3'-5' RNA processing and degradation in both the nucleus and the cytoplasm; has similarity to E. coli RNase PH and to human hRrp45p (PM/SCL-75, EXOSC9); protein abundance increases in response to DNA replication stress","termid":"PBO:0083850"}


id: GO:1990627
data:
  {"annotated_genes":["SJAG_02656"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104374],"is_not":false,"summary":null,"term":"GO:1990627"}]},"cv_name":"biological_process","definition":"The membrane organization process that joins two mitochondrial inner membranes to form a single membrane.","definition_xrefs":["GOC:vw","PMID:17055438"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner mitochondrial membrane organization","termid":"GO:0007007"},{"relation_name":"part_of","term_name":"mitochondrial fusion","termid":"GO:0008053"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02656":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007005"}],"interesting_parent_ids":["GO:0061024","GO:0008150","GO:0007005"],"is_obsolete":false,"name":"mitochondrial inner membrane fusion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrion inner membrane fusion","type":"exact"}],"termid":"GO:1990627","terms_by_termid":{"GO:1990627":null}}


id: PBO:0027264
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cell_growth","termid":"PBO:0027264"}


id: GO:0048710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of astrocyte differentiation.","definition_xrefs":["GOC:vp","PMID:15139015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glial cell differentiation","termid":"GO:0045685"},{"relation_name":"regulates","term_name":"astrocyte differentiation","termid":"GO:0048708"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of astrocyte differentiation","termid":"GO:0048710"}


id: GO:0045551
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cinnamyl alcohol + NADP+ = cinnamaldehyde + NADPH + H+. Also acts on coniferyl alcohol, sinapyl alcohol and 4-coumaryl alcohol.","definition_xrefs":["EC:1.1.1.195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"cinnamyl-alcohol dehydrogenase activity","secondary_identifiers":["MetaCyc:CINNAMYL-ALCOHOL-DEHYDROGENASE-RXN"],"synonyms":[{"name":"CAD activity","type":"broad"},{"name":"cinnamyl alcohol dehydrogenase activity","type":"related"},{"name":"cinnamyl-alcohol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0045551"}


id: PBO:0086550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved among S. cerevisiae strains; YEL028W is not an essential gene","termid":"PBO:0086550"}


id: PBO:0036292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine ribohydrolase Urh2 (predicted)","termid":"PBO:0036292"}


id: MONDO:0011093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive lysosomal storage disease caused by mutation(s) in the HYAL1 gene, encoding hyaluronidase-1. It is characterized by short stature and hyaluronidase deficiency.","definition_xrefs":["NCIT:C129073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"},{"relation_name":"is_a","term_name":"mucopolysaccharidosis","termid":"MONDO:0019249"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561","MONDO:0037792"],"is_obsolete":false,"name":"mucopolysaccharidosis type 9","secondary_identifiers":["OMIM:601492","NANDO:1200115","GARD:16675","DOID:0050809","Orphanet:67041","SCTID:124473006","icd11.foundation:952591271","MEDGEN:226942","MESH:C563209","ICD9:277.6","UMLS:C1291490"],"synonyms":[{"name":"MPS 9","type":"related"},{"name":"MPS9","type":"exact"},{"name":"MPSIX","type":"exact"},{"name":"hyaluronidase deficiency","type":"related"},{"name":"mucopolysaccharidosis IX","type":"related"},{"name":"mucopolysaccharidosis type 9","type":"exact"},{"name":"mucopolysaccharidosis type IX","type":"exact"},{"name":"mucopolysaccharidosis, type 9","type":"related"},{"name":"mucopolysaccharidosis, type IX","type":"related"}],"termid":"MONDO:0011093","xrefs":{"Monarch":{"xref_id":"0011093"}}}


id: PBO:0066255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMX2 pseudogene 3","termid":"PBO:0066255"}


id: PBO:0043550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type IV alpha 1 chain","termid":"PBO:0043550"}


id: GO:0060718
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells of the ectoplacental cone acquire specialized structural and/or functional features that characterize chorionic trophoblasts. These cells will migrate towards the spongiotrophoblast layer and give rise to syncytiotrophoblasts of the labyrinthine layer.","definition_xrefs":["GOC:dph","CL:0011101","PMID:16983341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"chorion development","termid":"GO:0060717"}],"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":"chorionic trophoblast cell differentiation","termid":"GO:0060718"}


id: MONDO:0012914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"1q21.1 microdeletion syndrome is a newly described recurrent deletion syndrome with variable clinical manifestations but without the clinical picture of thrombocytopenia - absent radius (TAR) syndrome.","definition_xrefs":["Orphanet:250989"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 1q deletion","termid":"MONDO:0022756"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1q21.1 deletion syndrome","secondary_identifiers":["DECIPHER:62","ICD9:758.33","DOID:0060411","MEDGEN:393913","SCTID:699305004","UMLS:C2675897","GARD:10813","OMIM:612474"],"synonyms":[{"name":"1q21.1 microdeletion","type":"related"},{"name":"1q21.1 microdeletion syndrome","type":"exact"},{"name":"1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders)","type":"exact"},{"name":"Del(1)(q21)","type":"exact"},{"name":"chromosome 1q21.1 deletion syndrome, 1.35-MB","type":"related"},{"name":"chromosome 1q21.1 deletion syndrome, isolated cases","type":"exact"},{"name":"chromosome 1q21.1 microdeletion syndrome","type":"related"},{"name":"monosomy 1q21.1","type":"exact"}],"termid":"MONDO:0012914","xrefs":{"Monarch":{"xref_id":"0012914"}}}


id: GO:0032882
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 chitin.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polysaccharide metabolic process","termid":"GO:0032881"},{"relation_name":"regulates","term_name":"chitin metabolic process","termid":"GO:0006030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"regulation of chitin metabolic process","synonyms":[{"name":"regulation of chitin metabolism","type":"exact"}],"termid":"GO:0032882"}


id: PBO:0073338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family A member 15, pseudogene","termid":"PBO:0073338"}


id: PATO:0000210
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000210 excretory function (obsolete PATO:0000210)","termid":"PATO:0000210"}


id: PBO:0047827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box P1","termid":"PBO:0047827"}


id: GO:0008622
data:
  {"annotated_genes":["SJAG_02908","SJAG_02667","SJAG_01823","SJAG_04879"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[106808,109400,113003,114847],"is_not":false,"summary":null,"term":"GO:0008622"}]},"cv_name":"cellular_component","definition":"A heterotetrameric DNA polymerase complex that catalyzes processive DNA synthesis in the absence of PCNA, but is further stimulated in the presence of PCNA. The complex contains a large catalytic subunit and three small subunits, and is best characterized in Saccharomyces, in which the subunits are named Pol2p, Dpb2p, Dpb3p, and Dpb4p. Some evidence suggests that DNA polymerase epsilon is the leading strand polymerase; it is also involved in nucleotide-excision repair and mismatch repair.","definition_xrefs":["PMID:15814431","PMID:9745046"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA polymerase complex","termid":"GO:0042575"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear chromosome","termid":"GO:0000228"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01823":null,"SJAG_02667":null,"SJAG_02908":null,"SJAG_04879":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005694","GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"epsilon DNA polymerase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA polymerase epsilon complex","type":"exact"}],"termid":"GO:0008622","terms_by_termid":{"GO:0008622":null}}


id: PBO:0077246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane and coiled-coil domains 6","termid":"PBO:0077246"}


id: GO:0019980
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to interleukin-5.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"},{"relation_name":"is_a","term_name":"cytokine binding","termid":"GO:0019955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"interleukin-5 binding","synonyms":[{"name":"IL-5 binding","type":"exact"}],"termid":"GO:0019980"}


id: PBO:0069744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1025, pseudogene","termid":"PBO:0069744"}


id: FYPO:0003624
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of threonine residues of one or more specific proteins is decreased during a cellular response to heat.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete decreased protein threonine phosphorylation during cellular response to heat (obsolete FYPO:0003624)","synonyms":[{"name":"decreased protein threonine phosphorylation during cellular response to heat during mitotic cell cycle","type":"related"},{"name":"decreased protein threonine phosphorylation during cellular response to heat during vegetative growth","type":"exact"},{"name":"reduced protein threonine phosphorylation during cellular response to heat","type":"exact"}],"termid":"FYPO:0003624"}


id: PBO:0053197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LETM1 domain containing 1","termid":"PBO:0053197"}


id: PBO:0057607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 941-4","termid":"PBO:0057607"}


id: MONDO:0036870
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm arising from the lymphatic vessels.","definition_xrefs":["NCIT:C3723"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"},{"relation_name":"is_a","term_name":"lymphatic system disorder","termid":"MONDO:0005833"},{"relation_name":"is_a","term_name":"vascular neoplasm","termid":"MONDO:0024296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"lymphatic vessel neoplasm","secondary_identifiers":["MEDGEN:64616","UMLS:C0206619"],"synonyms":[{"name":"lymph vessel neoplasm","type":"exact"},{"name":"lymph vessel tumor","type":"exact"},{"name":"lymph vessel tumour","type":"exact"},{"name":"lymphatic vessel neoplasm","type":"exact"},{"name":"lymphatic vessel tumor","type":"exact"},{"name":"lymphatic vessel tumour","type":"exact"},{"name":"neoplasm of lymph vessel","type":"exact"},{"name":"neoplasm of lymphatic vessel","type":"exact"},{"name":"neoplasm of the lymph vessel","type":"exact"},{"name":"neoplasm of the lymphatic vessel","type":"exact"},{"name":"tumor of lymph vessel","type":"exact"},{"name":"tumor of lymphatic vessel","type":"exact"},{"name":"tumor of the lymph vessel","type":"exact"},{"name":"tumor of the lymphatic vessel","type":"exact"},{"name":"tumour of lymph vessel","type":"exact"},{"name":"tumour of lymphatic vessel","type":"exact"},{"name":"tumour of the lymph vessel","type":"exact"},{"name":"tumour of the lymphatic vessel","type":"exact"}],"termid":"MONDO:0036870","xrefs":{"Monarch":{"xref_id":"0036870"}}}


id: GO:0052005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the normal execution of the ethylene-mediated defense response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host defenses","termid":"GO:0044414"},{"relation_name":"is_a","term_name":"symbiont-mediated modulation of host ethylene-mediated defense response","termid":"GO:0052084"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host ethylene-mediated defense response","secondary_identifiers":["GO:0052070","GO:0052254","GO:0052268"],"synonyms":[{"name":"down regulation by symbiont of host ethylene-mediated defense response","type":"exact"},{"name":"down-regulation by symbiont of host ethylene-mediated defense response","type":"exact"},{"name":"downregulation by symbiont of host ethylene-mediated defense response","type":"exact"},{"name":"inhibition by symbiont of host ethylene-mediated defense response","type":"narrow"},{"name":"negative regulation by organism of defense-related ethylene-mediated signal transduction pathway in other organism involved in symbiotic interaction","type":"broad"},{"name":"negative regulation by organism of ethylene-mediated defense response of other organism involved in symbiotic interaction","type":"broad"},{"name":"negative regulation by symbiont of defense-related host ethylene-mediated signal transduction pathway","type":"broad"},{"name":"negative regulation by symbiont of host ethylene-mediated defense response","type":"exact"},{"name":"suppression by organism of host ethylene-mediated defense response","type":"exact"},{"name":"suppression by symbiont of host ethylene-mediated defense response","type":"exact"}],"termid":"GO:0052005"}


id: PBO:0090726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L24","termid":"PBO:0090726"}


id: PBO:0047200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 217 member A","termid":"PBO:0047200"}


id: PBO:0072424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 29","termid":"PBO:0072424"}


id: GO:0034804
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: benzo(a)pyrene + O2 = benzo(a)pyrene-11,12-epoxide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete benzo(a)pyrene 11,12-epoxidase activity (obsolete GO:0034804)","termid":"GO:0034804"}


id: PBO:0116191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-oxoprolinase (ATP-hydrolizing), Oxp1","termid":"PBO:0116191"}


id: PBO:0065972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD52 pseudogene 1","termid":"PBO:0065972"}


id: GO:0060958
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of an endocardial cell over time, from its formation to the mature 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 development","termid":"GO:0001885"},{"relation_name":"is_a","term_name":"cardiac cell development","termid":"GO:0055006"},{"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 development","termid":"GO:0060958"}


id: PBO:0056576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microspherule protein 1","termid":"PBO:0056576"}


id: GO:1904236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of substrate-dependent cell migration, cell attachment to substrate.","definition_xrefs":["GOC:TermGenie","PMID:25834989","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell-substrate adhesion","termid":"GO:0010812"},{"relation_name":"is_a","term_name":"negative regulation of cell migration","termid":"GO:0030336"},{"relation_name":"is_a","term_name":"regulation of substrate-dependent cell migration, cell attachment to substrate","termid":"GO:1904235"},{"relation_name":"negatively_regulates","term_name":"substrate-dependent cell migration, cell attachment to substrate","termid":"GO:0006931"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of substrate-dependent cell migration, cell attachment to substrate","synonyms":[{"name":"down regulation of substrate-bound cell migration, cell attachment to substrate","type":"exact"},{"name":"down regulation of substrate-dependent cell migration, cell attachment to substrate","type":"exact"},{"name":"down-regulation of substrate-bound cell migration, cell attachment to substrate","type":"exact"},{"name":"down-regulation of substrate-dependent cell migration, cell attachment to substrate","type":"exact"},{"name":"downregulation of substrate-bound cell migration, cell attachment to substrate","type":"exact"},{"name":"downregulation of substrate-dependent cell migration, cell attachment to substrate","type":"exact"},{"name":"inhibition of substrate-bound cell migration, cell attachment to substrate","type":"narrow"},{"name":"inhibition of substrate-dependent cell migration, cell attachment to substrate","type":"narrow"},{"name":"negative regulation of substrate-bound cell migration, cell attachment to substrate","type":"exact"}],"termid":"GO:1904236"}


id: GO:1902982
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any DNA strand elongation involved in meiotic cell cycle DNA replication.","definition_xrefs":["GOC:TermGenie","GO_REF:0000060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA strand elongation involved in nuclear cell cycle DNA replication","termid":"GO:1902319"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"premeiotic DNA replication","termid":"GO:0006279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006260","GO:0006259","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"DNA strand elongation involved in premeiotic DNA replication","synonyms":[{"name":"DNA strand elongation involved in meiotic cell cycle DNA replication","type":"exact"}],"termid":"GO:1902982"}


id: MONDO:0014186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the ARL2BP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066","MONDO:0005328"],"is_obsolete":false,"name":"retinitis pigmentosa with or without situs inversus","secondary_identifiers":["MEDGEN:1658130","ICD10CM:H35.5","OMIM:615434","DOID:0110419","UMLS:C4747737","GARD:15965"],"synonyms":[{"name":"ARL2BP retinitis pigmentosa","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in ARL2BP","type":"exact"},{"name":"retinitis pigmentosa with or without situs inversus","type":"exact"}],"termid":"MONDO:0014186","xrefs":{"Monarch":{"xref_id":"0014186"}}}


id: PATO:0002168
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An angular placement quality inhering in a bearer by virtue of the bearer being changed in position in relation to another entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orientation","termid":"PATO:0000133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"displaced to","synonyms":[{"name":"mislocalised to","type":"related"}],"termid":"PATO:0002168"}


id: MONDO:0032014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A set of phenotypic abnormalities presenting in a subset of patients under particular circumstances.","definition_xrefs":["Orphanet:377793"],"gene_count":0,"genotype_count":0,"name":"obsolete particular clinical situation in a disease or syndrome (obsolete MONDO:0032014)","termid":"MONDO:0032014","xrefs":{"Monarch":{"xref_id":"0032014"}}}


id: GO:0061284
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the proximal tubule of the mesonephric nephron acquires its identity.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of mesonephric nephron tubule identity","termid":"GO:0061282"},{"relation_name":"is_a","term_name":"specification of proximal tubule identity","termid":"GO:0072082"},{"relation_name":"part_of","term_name":"mesonephric proximal tubule morphogenesis","termid":"GO:0061276"}],"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":"specification of mesonephric proximal tubule identity","termid":"GO:0061284"}


id: PBO:0031275
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_flocculation","termid":"PBO:0031275"}


id: PBO:0028360
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_polynucleotide_5'-phosphatase_activity","termid":"PBO:0028360"}


id: PBO:0083697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Epsilon subunit of the F1 sector of mitochondrial F1F0 ATP synthase; which is a large, evolutionarily conserved enzyme complex required for ATP synthesis; F1 translationally regulates ATP6 and ATP8 expression to achieve a balanced output of ATP synthase genes encoded in nucleus and mitochondria; phosphorylated","termid":"PBO:0083697"}


id: GO:0102716
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A28 + 2-oxoglutarate + O2 = (2betaOH)-gibberellin28 + succinate + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A28,oxoglutarate:oxygen oxidoreductase activity (obsolete GO:0102716)","termid":"GO:0102716"}


id: PBO:0110382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLHL5 pseudogene 1","termid":"PBO:0110382"}


id: GO:0097458
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any constituent part of a neuron, the basic cellular unit of nervous tissue. A typical neuron consists of a cell body (often called the soma), an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the nervous system.","definition_xrefs":["Wikipedia:Neuron","GOC:pr"],"gene_count":0,"genotype_count":0,"name":"obsolete neuron part (obsolete GO:0097458)","termid":"GO:0097458"}


id: FYPO:0006109
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 small interfering RNA transcripts derived from subtelomeric regions are present at greater levels than normal.","definition_xrefs":["PMID:28404620","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased siRNA level","termid":"FYPO:0004207"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"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:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0006551","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased subtelomeric transcript-derived siRNA level","synonyms":[{"name":"increased accumulation of siRNAs homologous to subtelomeres","type":"related"},{"name":"increased accumulation of subtelomeric transcript-derived siRNA","type":"exact"},{"name":"increased level of subtelomeric transcript-derived siRNA","type":"exact"},{"name":"increased subtelomere transcript-derived siRNA level","type":"exact"},{"name":"increased subtelomeric transcript-derived siRNA level during mitotic cell cycle","type":"related"},{"name":"increased subtelomeric transcript-derived siRNA level during vegetative growth","type":"exact"}],"termid":"FYPO:0006109"}


id: PBO:0031720
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitochondrial_genome_maintenance","termid":"PBO:0031720"}


id: GO:0070742
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a C2H2-type zinc finger domain of a protein. The C2H2 zinc finger is the classical zinc finger domain, in which two conserved cysteines and histidines co-ordinate a zinc ion.","definition_xrefs":["GOC:mah","GOC:BHF","Pfam:PF00096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"C2H2 zinc finger domain binding","termid":"GO:0070742"}


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


id: MONDO:0005730
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection with nematodes of the genus dictyocaulus. In deer, cattle, sheep, and horses the bronchi are the site of infestation.","definition_xrefs":["MESH:D004022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trichostrongyloidiasis, non-human animal","termid":"MONDO:0700204"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dictyocaulus infectious disease","secondary_identifiers":["MONDO:0025190"],"synonyms":[{"name":"Dictyocauliases","type":"related"},{"name":"Dictyocauliasis","type":"related"},{"name":"Dictyocaulus caused disease or disorder","type":"exact"},{"name":"Dictyocaulus disease or disorder","type":"exact"},{"name":"Dictyocaulus infection","type":"related"},{"name":"infection, Dictyocaulus","type":"related"},{"name":"infections, Dictyocaulus","type":"related"}],"termid":"MONDO:0005730","xrefs":{"Monarch":{"xref_id":"0005730"}}}


id: _global:directly_associated_with
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"q1 directly_associated_with q2 iff q1 is dependent on q2, and the magnitude of q1 increases if the magnitude of q2 is increased, or the magnitude of q1 decreases if the magnitude of q2 is decreased. The relationship is not necessarily linear.","definition_xrefs":["Wikipedia:Association_(statistics)","PATOC:cjm"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"directly_associated_with","termid":"_global:directly_associated_with"}


id: GO:2001072
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to galactomannan.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heteropolysaccharide binding","termid":"GO:0010297"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"galactomannan binding","termid":"GO:2001072"}


id: PBO:0079707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquilin 1 pseudogene 1","termid":"PBO:0079707"}


id: MONDO:0004753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"strabismus","termid":"MONDO:0003432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mechanical strabismus","secondary_identifiers":["ICD9:378.60","MEDGEN:101828","DOID:9306","ICD10CM:H50.6","icd11.foundation:230827382","ICD9:378.6","SCTID:5371001","UMLS:C0152223"],"termid":"MONDO:0004753","xrefs":{"Monarch":{"xref_id":"0004753"}}}


id: FYPO:0000402
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of progression through the G2/M transition of the mitotic cell cycle is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic G2/M phase transition","termid":"FYPO:0000399"}],"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:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000631","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"increased mitotic G2/M phase transition","synonyms":[{"name":"cell cycle progression through the G2/M phase transition: increased","type":"related"},{"name":"increased G2/M phase transition during mitotic cell cycle","type":"exact"},{"name":"increased cell cycle progression through mitotic G2/M phase transition","type":"exact"},{"name":"increased occurrence of mitotic G2/M phase transition during vegetative growth","type":"exact"}],"termid":"FYPO:0000402"}


id: MONDO:0859366
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"hearing loss, autosomal dominant 85","secondary_identifiers":["OMIM:620227","MEDGEN:1824075","UMLS:C5774302"],"synonyms":[{"name":"deafness, autosomal dominant 85","type":"narrow"}],"termid":"MONDO:0859366","xrefs":{"Monarch":{"xref_id":"0859366"}}}


id: GO:1900244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of synaptic vesicle endocytosis.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endocytosis","termid":"GO:0045807"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle endocytosis","termid":"GO:1900242"},{"relation_name":"is_a","term_name":"positive regulation of synaptic vesicle recycling","termid":"GO:1903423"},{"relation_name":"positively_regulates","term_name":"synaptic vesicle endocytosis","termid":"GO:0048488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"positive regulation of synaptic vesicle endocytosis","synonyms":[{"name":"activation of synaptic vesicle endocytosis","type":"narrow"},{"name":"activation of synaptic vesicle retrieval","type":"related"},{"name":"positive regulation of synaptic vesicle retrieval","type":"related"},{"name":"up regulation of synaptic vesicle endocytosis","type":"exact"},{"name":"up regulation of synaptic vesicle retrieval","type":"related"},{"name":"up-regulation of synaptic vesicle endocytosis","type":"exact"},{"name":"up-regulation of synaptic vesicle retrieval","type":"related"},{"name":"upregulation of synaptic vesicle endocytosis","type":"exact"},{"name":"upregulation of synaptic vesicle retrieval","type":"related"}],"termid":"GO:1900244"}


id: GO:0051846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any mechanism of immune avoidance that directly affects the symbiont immune system, e.g. blocking any stage in symbiont MHC class I and II presentation. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:12439615"],"gene_count":0,"genotype_count":0,"name":"obsolete active evasion of symbiont immune response (obsolete GO:0051846)","synonyms":[{"name":"active evasion of symbiont immune response","type":"exact"},{"name":"active immune evasion","type":"broad"}],"termid":"GO:0051846"}


id: GO:0035943
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of estrone into the circulatory system.","definition_xrefs":["GOC:sl","PMID:8395854"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"},{"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:0008150"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"estrone secretion","synonyms":[{"name":"3-hydroxy-1,3,5(10)-estratrien-17-one secretion","type":"exact"},{"name":"folliculin secretion","type":"exact"}],"termid":"GO:0035943"}


id: GO:0015381
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the secondary active high affinity transfer of sulfate from one side of a membrane to the other. Secondary active transport is the transfer of a solute across a membrane, up its concentration gradient. The transporter binds the solute and undergoes a series of conformational changes. Transport works equally well in either direction and is driven by a chemiosmotic source of energy. Secondary active transporters include symporters and antiporters. In high-affinity transport the transporter is able to bind thesolute even if it is only present at very low concentrations.","definition_xrefs":["GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary active sulfate transmembrane transporter activity","termid":"GO:0008271"}],"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:0003674","GO:0005215"],"is_obsolete":false,"name":"high-affinity sulfate transmembrane transporter activity","synonyms":[{"name":"high affinity sulfate permease activity","type":"related"},{"name":"high affinity sulfate transmembrane transporter activity","type":"exact"},{"name":"high affinity sulphate permease activity","type":"exact"}],"termid":"GO:0015381"}


id: PBO:0060062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 9","termid":"PBO:0060062"}


id: GO:0003211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of a cardiac ventricle from unspecified parts. A cardiac ventricle receives blood from a cardiac atrium and pumps it out of the heart.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac chamber formation","termid":"GO:0003207"},{"relation_name":"part_of","term_name":"cardiac ventricle morphogenesis","termid":"GO:0003208"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cardiac ventricle formation","termid":"GO:0003211"}


id: PBO:0058697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6825","termid":"PBO:0058697"}


id: PATO:0002358
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An elongated raised margin or border.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ridged","synonyms":[{"name":"ridge-like","type":"exact"}],"termid":"PATO:0002358"}


id: PBO:0059804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 30","termid":"PBO:0059804"}


id: PBO:0074070
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 45","termid":"PBO:0074070"}


id: PBO:0080517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WASF3 antisense RNA 1","termid":"PBO:0080517"}


id: PBO:0049821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HDAC11 antisense RNA 1","termid":"PBO:0049821"}


id: MONDO:0017778
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A keratinization disorder characterized by the presence of large scales all over the body without significant erythroderma.","definition_xrefs":["Orphanet:313"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"ichthyosis","termid":"MONDO:0019269"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"lamellar ichthyosis","secondary_identifiers":["icd11.foundation:600146417","NCIT:C84805","MedDRA:10023686","NANDO:1200617","GARD:10803","MEDGEN:1852191","UMLS:C5848247","NORD:1289"],"synonyms":[{"name":"LI","type":"exact"},{"name":"classic lamellar ichthyosis","type":"exact"},{"name":"congenital lamellar ichthyosis","type":"exact"}],"termid":"MONDO:0017778","xrefs":{"Monarch":{"xref_id":"0017778"}}}


id: GO:1901716
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of gamma-aminobutyric acid catabolic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"negative regulation of amino acid metabolic process","termid":"GO:0045763"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of gamma-aminobutyric acid catabolic process","termid":"GO:1901715"},{"relation_name":"negatively_regulates","term_name":"gamma-aminobutyric acid catabolic process","termid":"GO:0009450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044248"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"negatively_regulates","termid":"GO:0044248"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044248","GO:0044281"],"is_obsolete":false,"name":"negative regulation of gamma-aminobutyric acid catabolic process","synonyms":[{"name":"down regulation of 4-aminobutanoate catabolic process","type":"exact"},{"name":"down regulation of 4-aminobutanoate catabolism","type":"exact"},{"name":"down regulation of 4-aminobutyrate catabolic process","type":"exact"},{"name":"down regulation of 4-aminobutyrate catabolism","type":"exact"},{"name":"down regulation of GABA catabolic process","type":"exact"},{"name":"down regulation of GABA catabolism","type":"exact"},{"name":"down regulation of gamma-aminobutyric acid breakdown","type":"exact"},{"name":"down regulation of gamma-aminobutyric acid catabolic process","type":"exact"},{"name":"down regulation of gamma-aminobutyric acid catabolism","type":"exact"},{"name":"down regulation of gamma-aminobutyric acid degradation","type":"exact"},{"name":"down-regulation of 4-aminobutanoate catabolic process","type":"exact"},{"name":"down-regulation of 4-aminobutanoate catabolism","type":"exact"},{"name":"down-regulation of 4-aminobutyrate catabolic process","type":"exact"},{"name":"down-regulation of 4-aminobutyrate catabolism","type":"exact"},{"name":"down-regulation of GABA catabolic process","type":"exact"},{"name":"down-regulation of GABA catabolism","type":"exact"},{"name":"down-regulation of gamma-aminobutyric acid breakdown","type":"exact"},{"name":"down-regulation of gamma-aminobutyric acid catabolic process","type":"exact"},{"name":"down-regulation of gamma-aminobutyric acid catabolism","type":"exact"},{"name":"down-regulation of gamma-aminobutyric acid degradation","type":"exact"},{"name":"downregulation of 4-aminobutanoate catabolic process","type":"exact"},{"name":"downregulation of 4-aminobutanoate catabolism","type":"exact"},{"name":"downregulation of 4-aminobutyrate catabolic process","type":"exact"},{"name":"downregulation of 4-aminobutyrate catabolism","type":"exact"},{"name":"downregulation of GABA catabolic process","type":"exact"},{"name":"downregulation of GABA catabolism","type":"exact"},{"name":"downregulation of gamma-aminobutyric acid breakdown","type":"exact"},{"name":"downregulation of gamma-aminobutyric acid catabolic process","type":"exact"},{"name":"downregulation of gamma-aminobutyric acid catabolism","type":"exact"},{"name":"downregulation of gamma-aminobutyric acid degradation","type":"exact"},{"name":"inhibition of 4-aminobutanoate catabolic process","type":"exact"},{"name":"inhibition of 4-aminobutanoate catabolism","type":"exact"},{"name":"inhibition of 4-aminobutyrate catabolic process","type":"exact"},{"name":"inhibition of 4-aminobutyrate catabolism","type":"exact"},{"name":"inhibition of GABA catabolic process","type":"exact"},{"name":"inhibition of GABA catabolism","type":"exact"},{"name":"inhibition of gamma-aminobutyric acid breakdown","type":"exact"},{"name":"inhibition of gamma-aminobutyric acid catabolic process","type":"narrow"},{"name":"inhibition of gamma-aminobutyric acid catabolism","type":"exact"},{"name":"inhibition of gamma-aminobutyric acid degradation","type":"exact"},{"name":"negative regulation of 4-aminobutanoate catabolic process","type":"exact"},{"name":"negative regulation of 4-aminobutanoate catabolism","type":"exact"},{"name":"negative regulation of 4-aminobutyrate catabolic process","type":"exact"},{"name":"negative regulation of 4-aminobutyrate catabolism","type":"exact"},{"name":"negative regulation of GABA catabolic process","type":"exact"},{"name":"negative regulation of GABA catabolism","type":"exact"},{"name":"negative regulation of gamma-aminobutyric acid breakdown","type":"exact"},{"name":"negative regulation of gamma-aminobutyric acid catabolism","type":"exact"},{"name":"negative regulation of gamma-aminobutyric acid degradation","type":"exact"}],"termid":"GO:1901716"}


id: PBO:0067653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 828, pseudogene","termid":"PBO:0067653"}


id: PBO:0059430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane spanning 4-domains A1","termid":"PBO:0059430"}


id: GO:0015721
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of bile acid and bile salts into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:dph","GOC:krc","PMID:14699511","PMID:12663868"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transport","termid":"GO:0006869"},{"relation_name":"is_a","term_name":"monocarboxylic acid transport","termid":"GO:0015718"},{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"bile acid and bile salt transport","secondary_identifiers":["Reactome:R-HSA-159418"],"synonyms":[{"name":"bile acid transport","type":"narrow"},{"name":"bile salt transport","type":"narrow"}],"termid":"GO:0015721"}


id: MONDO:0016687
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare variant of diffuse astrocytoma. It is predominantly composed of neoplastic astrocytes showing a small cell body with few, flaccid processes with a low content of glial filaments and scant GFAP expression. This lesion is not well defined and is considered by some authors as an occasional histopathological feature rather than a reproducibly identifiable variant. When occurring in children, this neoplasm may be difficult to separate from pilocytic juvenile astrocytoma. (Adapted from WHO)","definition_xrefs":["NCIT:C4320"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse astrocytoma","termid":"MONDO:0016686"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protoplasmic astrocytoma","secondary_identifiers":["MEDGEN:87268","DOID:7008","GARD:20707","ICDO:9410/3","Orphanet:251598","UMLS:C0334580"],"synonyms":[{"name":"protoplasmic astrocytic tumor","type":"exact"},{"name":"protoplasmic astrocytic tumour","type":"exact"},{"name":"protoplasmic astrocytoma","type":"exact"},{"name":"protoplasmic astrocytoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0016687","xrefs":{"Monarch":{"xref_id":"0016687"}}}


id: PBO:0054449
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 1846","termid":"PBO:0054449"}


id: PBO:0089506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RecQ mediated genome instability protein Rmi1","termid":"PBO:0089506"}


id: MONDO:0020412
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital patent ductus arteriosus aneurysm is a rare, congenital, arterial duct anomaly characterized by a saccular dilatation of the ductus arteriosus. It is often asymptomatic or presents shortly after birth with respiratory distress, stridor, cyanosis and/or weak cry. Complications, such as rupture, thromboembolism, infection, airway erosion and/or compression of the adjacent thoracic structures, can develop. Spontaneous resolution has been reported.","definition_xrefs":["Orphanet:99072"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital anomaly of the great arteries","termid":"MONDO:0020292"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital patent ductus arteriosus aneurysm","secondary_identifiers":["GARD:19634","SCTID:763316006","UMLS:C4706391","MEDGEN:1646456"],"termid":"MONDO:0020412","xrefs":{"Monarch":{"xref_id":"0020412"}}}


id: GO:0052841
data:
  {"annotated_genes":["SJAG_04870","SJAG_00244","SJAG_01154"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104668,88237,114502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052846"},{"annotations":[88238,104669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052847"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: bisdiphospho-1D-myo-inositol tetrakisphosphate + H2O = diphospho-1D-myo-inositol pentakisphosphate + phosphate.","definition_xrefs":["PMID:11502751","PMID:10827188"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diphosphoinositol-polyphosphate diphosphatase activity","termid":"GO:0008486"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00244":null,"SJAG_01154":null,"SJAG_04870":null},"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:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"inositol bisdiphosphate tetrakisphosphate diphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-2023973","Reactome:R-HSA-1855165"],"termid":"GO:0052841","terms_by_termid":{"GO:0052846":null,"GO:0052847":null}}


id: RO:0002637
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of mesoparasite of","direct_ancestors":[{"relation_name":"is_a","term_name":"parasitized_by","termid":"RO:0002445"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_mesoparasite","termid":"RO:0002637"}


id: GO:0106320
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (4R)-limonene + NADPH + H+ + O2 = NADP+ + H2O + (4R)-limonene-1,2-epoxide.","definition_xrefs":["RHEA:26097"],"gene_count":0,"genotype_count":0,"name":"obsolete (R)-limonene 1,2-monooxygenase NADPH activity (obsolete GO:0106320)","termid":"GO:0106320"}


id: FYPO:0002170
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that is elongated and branched (and septated), and undergoes two or more rounds of cell division and then dies.","definition_xrefs":["PomBase:al","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, multiple cell divisions, elongated cell","termid":"FYPO:0002262"}],"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":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000004","FYPO:0000005","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination, multiple cell divisions, branched, elongated cell","synonyms":[{"name":"inviable after spore germination, multiple cell divisions, elongated and branched cell","type":"exact"},{"name":"inviable following spore germination, multiple cell divisions, branched, elongated cell","type":"exact"},{"name":"inviable germinated spore, multiple cell divisions, branched, elongated cell","type":"exact"},{"name":"lethal after spore germination, multiple cell divisions, branched, elongated cell","type":"exact"}],"termid":"FYPO:0002170"}


id: PR:O94728
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1604.16c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94728"],"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 C1604.16c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.16c","synonyms":[{"name":"Spom972h-SPBC1604.16c","type":"exact"}],"termid":"PR:O94728"}


id: GO:0060586
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A chemical homeostatic process involved in the maintenance of a steady state level of iron within extracellular body fluids, such as blood, xylem or phloem, of a multicellular organism. This is distinct from maintenance of cellular homeostasis, which occurs within a cell.","definition_xrefs":["PMID:31431773"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic cation homeostasis","termid":"GO:0055080"},{"relation_name":"is_a","term_name":"inorganic ion homeostasis","termid":"GO:0098771"},{"relation_name":"is_a","term_name":"multicellular organismal-level chemical homeostasis","termid":"GO:0140962"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098771"}],"interesting_parent_ids":["GO:0008150","GO:0098771"],"is_obsolete":false,"name":"multicellular organismal-level iron ion homeostasis","synonyms":[{"name":"multicellular organismal iron ion homeostasis","type":"exact"}],"termid":"GO:0060586"}


id: FYPO:0002160
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing cilofungin.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal growth on echinocandin","termid":"FYPO:0004892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002058","FYPO:0000257","FYPO:0002057","FYPO:0002060","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on cilofungin","synonyms":[{"name":"normal cell population growth in presence of cilofungin","type":"exact"},{"name":"normal cell population growth on cilofungin","type":"exact"},{"name":"normal cellular response to cilofungin","type":"related"},{"name":"normal vegetative cell population growth on cilofungin","type":"exact"}],"termid":"FYPO:0002160"}


id: PATO:0001774
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's having or existing in many phases.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phase","termid":"PATO:0000083"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyphasic","termid":"PATO:0001774"}


id: PBO:0029777
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_branched,_elongated_vegetative_cell","termid":"PBO:0029777"}


id: MONDO:0100467
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"preeclampsia","termid":"MONDO:0005081"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"preeclampsia/eclampsia 1","secondary_identifiers":["UMLS:C5574918","GARD:18389","MEDGEN:1807479","OMIM:189800"],"synonyms":[{"name":"PEE1","type":"exact"},{"name":"PREECLAMPSIA/eclampsia 1","type":"exact"},{"name":"PREG1","type":"exact"},{"name":"hemolysis, elevated liver enzymes, and low platelet count","type":"related"},{"name":"hypertension, pregnancy-induced","type":"related"},{"name":"toxaemia of pregnancy","type":"broad"},{"name":"toxemia of pregnancy","type":"broad"}],"termid":"MONDO:0100467","xrefs":{"Monarch":{"xref_id":"0100467"}}}


id: MONDO:0017278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues.","definition_xrefs":["NCIT:C129726"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of endocrine system","termid":"MONDO:0000569"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"polyendocrinopathy","termid":"MONDO:0015126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune polyendocrinopathy","secondary_identifiers":["Orphanet:282196","UMLS:C0085409","DOID:14040","ICD10CM:E31.0","ICD9:258.8","NCIT:C84576","icd11.foundation:548357900","GARD:21116","SCTID:41864002","NANDO:2100125","MEDGEN:39042","NORD:790"],"synonyms":[{"name":"APS","type":"exact"},{"name":"Antiphospholipid Syndrome","type":"exact"},{"name":"Lloyd's syndrome","type":"exact"},{"name":"autoimmune polyendocrine syndrome","type":"exact"},{"name":"autoimmune polyendocrine syndrome; polyglandular autoimmune syndrome","type":"exact"},{"name":"autoimmune polyendocrinopathy","type":"exact"},{"name":"autoimmune polyendocrinopathy syndrome","type":"exact"},{"name":"autoimmune polyglandular failure","type":"exact"},{"name":"autoimmune polyglandular syndrome","type":"exact"},{"name":"autoimmune polyglandular syndrome(s)","type":"exact"}],"termid":"MONDO:0017278","xrefs":{"Monarch":{"xref_id":"0017278"}}}


id: PBO:0043922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CROCC pseudogene 1","termid":"PBO:0043922"}


id: GO:2000418
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of eosinophil migration.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte migration","termid":"GO:0002687"},{"relation_name":"is_a","term_name":"regulation of eosinophil migration","termid":"GO:2000416"},{"relation_name":"positively_regulates","term_name":"eosinophil migration","termid":"GO:0072677"}],"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 eosinophil migration","termid":"GO:2000418"}


id: PBO:0036468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial F1-F0 ATPase synthase peripheral stalk assembly factor Ina17 (predicted)","termid":"PBO:0036468"}


id: PBO:0078915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gln (anticodon TTG) 4-1","termid":"PBO:0078915"}


id: PBO:0044453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily F member 32, pseudogene","termid":"PBO:0044453"}


id: PBO:0075026
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 115-37","termid":"PBO:0075026"}


id: MONDO:0005734
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease of horses and donkeys caused by Trypanosoma equiperdum. The disease occurs in Africa, the Americas, and Asia.","definition_xrefs":["MESH:D004313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"horse disease","termid":"MONDO:0024950"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dourine","secondary_identifiers":["SCTID:15566009"],"termid":"MONDO:0005734","xrefs":{"Monarch":{"xref_id":"0005734"}}}


id: MONDO:0004697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare condition that usually affects the middle-to-distal esophagus in middle-aged and elderly people. There is usually a history of tobacco smoking or alcohol intake. Dysphagia is the presenting symptom. Morphologically, the lesions are well-demarcated and are characterized by epithelial hyperplasia, thickened basal layer, prominent granular cell layer, and hyperorthokeratosis. In a minority of patients this condition is associated with adjacent high-grade squamous dysplasia and/or squamous cell carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal disorder","termid":"MONDO:0003749"},{"relation_name":"is_a","term_name":"leukoplakia","termid":"MONDO:0043243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"esophageal leukoplakia","secondary_identifiers":["NCIT:C3953","SCTID:89057003","UMLS:C0267095","HP:0012859","DOID:9021","ICD9:530.83","MEDGEN:75628"],"synonyms":[{"name":"esophageal epidermoid metaplasia","type":"exact"},{"name":"esophageal leukoplakia","type":"exact"},{"name":"esophageal leukoplakia (disease)","type":"exact"},{"name":"esophagus leukoplakia","type":"exact"},{"name":"leukoplakia of esophagus","type":"exact"},{"name":"leukoplakia of oesophagus","type":"exact"},{"name":"leukoplakia of the esophagus","type":"exact"},{"name":"leukoplakia of the oesophagus","type":"exact"},{"name":"oesophagus leukoplakia","type":"exact"}],"termid":"MONDO:0004697","xrefs":{"Monarch":{"xref_id":"0004697"}}}


id: PBO:0079972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP9Y pseudogene 10","termid":"PBO:0079972"}


id: GO:1990540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a manganese ion is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:12890866"],"direct_ancestors":[{"relation_name":"is_a","term_name":"manganese ion transmembrane transport","termid":"GO:0071421"},{"relation_name":"is_a","term_name":"mitochondrial transmembrane transport","termid":"GO:1990542"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"mitochondrial manganese ion transmembrane transport","termid":"GO:1990540"}


id: MONDO:0002064
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign diffuse vascular proliferation in the breast. It is characterized by the formation of capillary-sized and cavernous vascular spaces.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"capillary disorder","termid":"MONDO:0001574"},{"relation_name":"is_a","term_name":"breast disorder","termid":"MONDO:0002657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast angiomatosis","secondary_identifiers":["MEDGEN:307304","UMLS:C1511284","DOID:1637","NCIT:C40381"],"termid":"MONDO:0002064","xrefs":{"Monarch":{"xref_id":"0002064"}}}


id: PBO:0027713
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_branched,_swollen,_elongated_vegetative_cell","termid":"PBO:0027713"}


id: PBO:0065378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pregnancy specific beta-1-glycoprotein 6","termid":"PBO:0065378"}


id: PBO:0080659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WAP four-disulfide core domain 3","termid":"PBO:0080659"}


id: MONDO:1011186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Scoliosis that occurs in chicken.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"scoliosis, non-human animal","termid":"MONDO:1010302"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scoliosis, chicken","secondary_identifiers":["OMIA:000891-9031"],"termid":"MONDO:1011186","xrefs":{"Monarch":{"xref_id":"1011186"}}}


id: MONDO:0023164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pericarditis that is caused by an infection with a viral agent.","definition_xrefs":["NCIT:C128405"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pericarditis","termid":"MONDO:0005904"},{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"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":"viral pericarditis","secondary_identifiers":["icd11.foundation:624707101","SCTID:70189005","UMLS:C0276139","MEDGEN:547113"],"synonyms":[{"name":"Viral Pericarditis","type":"related"},{"name":"Viral pericarditis","type":"related"},{"name":"viral pericarditis","type":"exact"}],"termid":"MONDO:0023164","xrefs":{"Monarch":{"xref_id":"0023164"}}}


id: GO:0061045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of the series of events that restore integrity to a damaged tissue, following an injury.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to external stimulus","termid":"GO:0032102"},{"relation_name":"is_a","term_name":"regulation of wound healing","termid":"GO:0061041"},{"relation_name":"is_a","term_name":"negative regulation of response to wounding","termid":"GO:1903035"},{"relation_name":"negatively_regulates","term_name":"wound healing","termid":"GO:0042060"}],"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 wound healing","termid":"GO:0061045"}


id: PBO:0090036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF3844 family transmembrane protein, conserved in fungi","termid":"PBO:0090036"}


id: PBO:0005052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudogene wtf element Wtf3 (no methionine)","termid":"PBO:0005052"}


id: MONDO:0031047
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Stickler syndrome","termid":"MONDO:0019354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005559","MONDO:0005497"],"is_obsolete":false,"name":"stickler syndrome, IIa 6","secondary_identifiers":["MEDGEN:1823980","OMIM:620022","UMLS:C5774207"],"synonyms":[{"name":"STL6","type":"exact"},{"name":"stickler syndrome, IIa 6","type":"exact"}],"termid":"MONDO:0031047","xrefs":{"Monarch":{"xref_id":"0031047"}}}


id: PATO:0000251
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000251 startle reflex (obsolete PATO:0000251)","termid":"PATO:0000251"}


id: PBO:0040296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase plasma membrane Ca2+ transporting 1","termid":"PBO:0040296"}


id: MONDO:0014313
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity","secondary_identifiers":["OMIM:615707","Orphanet:437552","GARD:17732","MEDGEN:816672","DOID:0111941","UMLS:C3810342"],"synonyms":[{"name":"CD16 deficiency","type":"exact"},{"name":"IMD20","type":"related"},{"name":"autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity","type":"exact"},{"name":"immunodeficiency 20","type":"related"},{"name":"immunodeficiency type 20","type":"exact"}],"termid":"MONDO:0014313","xrefs":{"Monarch":{"xref_id":"0014313"}}}


id: PBO:0056787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microfibril associated protein 3 like","termid":"PBO:0056787"}


id: GO:2000615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of histone H3-K9 acetylation.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone H3-K9 acetylation (obsolete GO:2000615)","synonyms":[{"name":"regulation of histone H3 acetylation at K9","type":"exact"},{"name":"regulation of histone H3K9 acetylation","type":"exact"}],"termid":"GO:2000615"}


id: SO:0000838
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of an rRNA primary transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary_transcript_region","termid":"SO:0000835"},{"relation_name":"part_of","term_name":"rRNA_primary_transcript","termid":"SO:0000209"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA_primary_transcript_region","synonyms":[{"name":"rRNA primary transcript region","type":"exact"}],"termid":"SO:0000838"}


id: GO:0009455
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a motile cell or organism in response to redox potential.","definition_xrefs":["PMID:11029423","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemotaxis","termid":"GO:0006935"},{"relation_name":"is_a","term_name":"energy taxis","termid":"GO:0009453"},{"relation_name":"is_a","term_name":"response to redox state","termid":"GO:0051775"}],"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":"redox taxis","synonyms":[{"name":"redoxtaxis","type":"exact"},{"name":"taxis in response to redox potential","type":"exact"},{"name":"taxis in response to redox stimulus","type":"exact"}],"termid":"GO:0009455"}


id: PBO:0082548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cell wall-related secretory glycoprotein; induced by nutrient deprivation-associated growth arrest and upon entry into stationary phase; may be involved in adaptation prior to stationary phase entry; protein demonstrates amyloid properties in vivo; YGP1 has a paralog, SPS100, that arose from the whole genome duplication","termid":"PBO:0082548"}


id: PBO:0051915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit beta 1 binding protein 2","termid":"PBO:0051915"}


id: GO:0072285
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transition where a mesenchymal cell establishes apical/basolateral polarity,forms intercellular adhesive junctions, synthesizes basement membrane components and becomes an epithelial cell that will contribute to the shaping of the metanephric renal vesicle.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesenchymal to epithelial transition involved in metanephros morphogenesis","termid":"GO:0003337"},{"relation_name":"is_a","term_name":"mesenchymal to epithelial transition involved in renal vesicle formation","termid":"GO:0072036"},{"relation_name":"part_of","term_name":"metanephric renal vesicle formation","termid":"GO:0072093"}],"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":"mesenchymal to epithelial transition involved in metanephric renal vesicle formation","termid":"GO:0072285"}


id: PBO:0061902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opioid related nociceptin receptor 1","termid":"PBO:0061902"}


id: MONDO:0001002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pulmonary siderosis (obsolete MONDO:0001002)","termid":"MONDO:0001002","xrefs":{"Monarch":{"xref_id":"0001002"}}}


id: GO:0036063
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cone-shaped structure in the head of a spermatozoon, which is formed by the coalescence of Golgi fragments following the completion of meiosis. The acroblast is situated adjacent to the acrosomal vesicle.","definition_xrefs":["PMID:19934220","GOC:sart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"Golgi apparatus","termid":"GO:0005794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005794","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"acroblast","synonyms":[{"name":"spermatid acroblast","type":"exact"}],"termid":"GO:0036063"}


id: PBO:0086164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for rRNA maturation and ribosomal subunit biogenesis; required for 18S rRNA maturation; also required for small ribosomal subunit biogenesis; cosediments with pre-ribosomal particles; mutation decreases efficiency of +1 Ty1 frameshifting and transposition, and affects budding pattern","termid":"PBO:0086164"}


id: PBO:0049206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate ionotropic receptor NMDA type subunit 1","termid":"PBO:0049206"}


id: GO:0046367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of allose, allo-hexose, an aldohexose similar to glucose, differing only in the configuration of the hydroxyl group of C-3.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete allose catabolic process (obsolete GO:0046367)","synonyms":[{"name":"allose breakdown","type":"exact"},{"name":"allose catabolism","type":"exact"},{"name":"allose degradation","type":"exact"}],"termid":"GO:0046367"}


id: MONDO:0011584
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations is a rare cancer-predisposing syndrome, associated with the D1 subgroup of Fanconi anemia (FA), characterized by progressive bone marrow failure, cardiac, brain, intestinal or skeletal abnormalities and predisposition to various malignancies. Bone marrow suppression and the incidence of developmental abnormalities are less frequent than in other FA, but cancer risk is very high with the spectrum of childhood cancers including Wilms tumor, brain tumor (often medulloblastoma) and ALL/AML.","definition_xrefs":["Orphanet:319462"],"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:0005046"},{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0002280","MONDO:0021190","MONDO:0005570","MONDO:0005066"],"is_obsolete":false,"name":"Fanconi anemia complementation group D1","secondary_identifiers":["SCTID:766707003","NCIT:C125705","UMLS:C1838457","OMIM:605724","MEDGEN:325420","DOID:0111089","GARD:17449","MESH:C563980"],"synonyms":[{"name":"FAD1","type":"exact"},{"name":"FANCD1","type":"exact"},{"name":"Fad1","type":"related"},{"name":"Fanconi anemia complementation group D1","type":"exact"},{"name":"Fanconi anemia, complementation group D1","type":"related"},{"name":"inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations","type":"related"}],"termid":"MONDO:0011584","xrefs":{"Monarch":{"xref_id":"0011584"}}}


id: MONDO:0011581
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cardioectodermal syndrome that is often associated with the gene DSP, encoding desmoplakin. Desmoplakin is a member of the plakin family of cell adhesion molecules that are responsible for the formation and maintenance of desmosomes. Variation in DSP is associated with cardiomyopathic manifestations that include: (1) seemingly isolated arrhythmogenic right ventricle cardiomyopathy (ARVC) that is atypical and can show left ventricle dominance, or be present in the left and right ventricle simultaneously; and (2) dilated cardiomyopathy. Cutaneous phenotypes including wooly hair and/or keratoderma can present along with the cardiomyopathy, but are noted as less penetrant features.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome associated with dilated cardiomyopathy (obsolete MONDO:0016337)","termid":"MONDO:0016337"},{"relation_name":"excluded_subClassOf","term_name":"focal palmoplantar keratoderma","termid":"MONDO:0017672"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome with wooly hair (obsolete MONDO:0018558)","termid":"MONDO:0018558"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"cardioectodermal syndrome","termid":"MONDO:0100080"}],"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":"arrhythmogenic cardiomyopathy with wooly hair and keratoderma","secondary_identifiers":["DOID:0090128","OMIM:605676","MEDGEN:340124","MESH:C535581","Orphanet:65282","UMLS:C1854063","GARD:5595","SCTID:719835006"],"synonyms":[{"name":"Carvajal syndrome","type":"exact"},{"name":"DCWHK","type":"exact"},{"name":"KWWH type II","type":"exact"},{"name":"arrhythmogenic cardiomyopathy with wooly hair and keratoderma","type":"exact"},{"name":"cardiomyopathy dilated with woolly hair and keratoderma","type":"related"},{"name":"cardiomyopathy dilated with wooly hair and keratoderma","type":"related"},{"name":"cardiomyopathy, dilated, with woolly hair and keratoderma","type":"related"},{"name":"cardiomyopathy, dilated, with wooly hair and keratoderma","type":"related"},{"name":"dilated cardiomyopathy with woolly hair and keratoderma","type":"exact"},{"name":"dilated cardiomyopathy with wooly hair and keratoderma","type":"exact"},{"name":"epidermolytic palmoplantar keratoderma woolly hair and dilated cardiomyopathy","type":"related"},{"name":"epidermolytic palmoplantar keratoderma wooly hair and dilated cardiomyopathy","type":"related"},{"name":"keratoderma with woolly hair type II","type":"exact"},{"name":"keratoderma with wooly hair type II","type":"exact"},{"name":"palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair","type":"exact"},{"name":"palmoplantar keratoderma with left ventricular cardiomyopathy and wooly hair","type":"exact"},{"name":"woolly hair - palmoplantar keratoderma - dilated cardiomyopathy","type":"related"},{"name":"woolly hair - palmoplantar keratoderma - dilated cardiomyopathy syndrome","type":"related"},{"name":"woolly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome","type":"exact"},{"name":"woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome","type":"exact"},{"name":"wooly hair - palmoplantar keratoderma - dilated cardiomyopathy","type":"related"},{"name":"wooly hair - palmoplantar keratoderma - dilated cardiomyopathy syndrome","type":"related"},{"name":"wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome","type":"exact"},{"name":"wooly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome","type":"exact"}],"termid":"MONDO:0011581","xrefs":{"Monarch":{"xref_id":"0011581"}}}


id: MONDO:0002411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by an enduring pattern of grandiose beliefs and arrogant behavior together with an overwhelming need for admiration and a lack of empathy for (and even exploitation of) others.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"personality disorder","termid":"MONDO:0002028"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"narcissistic personality disorder","secondary_identifiers":["ICD10CM:F60.81","NCIT:C92635","UMLS:C0027402","DOID:2745","icd11.foundation:641223668","ICD9:301.81","SCTID:80711002","MEDGEN:10262"],"termid":"MONDO:0002411","xrefs":{"Monarch":{"xref_id":"0002411"}}}


id: GO:1990078
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that inhibits multiple events of replication initiation during one replication cycle.","definition_xrefs":["GOC:bhm","PMID:21708944"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"replisome","termid":"GO:0030894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"replication inhibiting complex","termid":"GO:1990078"}


id: PBO:0078031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 21","termid":"PBO:0078031"}


id: GO:0043100
data:
  {"annotated_genes":["SJAG_04354"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91478],"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:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"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: GO:0038083
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The phosphorylation by a protein of one or more of its own tyrosine amino acid residues, or a tyrosine residue on an identical protein.","definition_xrefs":["PMID:10068444","PMID:10037737","PMID:10940390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-tyrosine phosphorylation","termid":"GO:0018108"},{"relation_name":"is_a","term_name":"protein autophosphorylation","termid":"GO:0046777"}],"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-tyrosine autophosphorylation","synonyms":[{"name":"RTK autophosphorylation","type":"narrow"},{"name":"receptor tyrosine kinase autophosphorylation","type":"narrow"},{"name":"tyrosine autophosphorylation","type":"exact"}],"termid":"GO:0038083"}


id: PBO:0031030
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_nucleolus_organization","termid":"PBO:0031030"}


id: MONDO:1012598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculocutaneous albinism that occurs in rabbits due to a mutation in the TYR gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism, non-human animal","termid":"MONDO:1012579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculocutaneous albinism, TYR-related, rabbit","secondary_identifiers":["OMIA:000202-9986"],"synonyms":[{"name":"coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related in Oryctolagus cuniculus (rabbit)","type":"exact"}],"termid":"MONDO:1012598","xrefs":{"Monarch":{"xref_id":"1012598"}}}


id: MONDO:0013186
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85973],"is_not":false,"summary":null,"term":"MONDO:0013186"}]},"cv_name":"mondo","definition":"Any Noonan syndrome in which the cause of the disease is a mutation in the NRAS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome","termid":"MONDO:0018997"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005267"],"is_obsolete":false,"name":"Noonan syndrome 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C176934","OMIM:613224","MEDGEN:413028","UMLS:C2750732","GARD:10701","DOID:0060584","MESH:C548084"],"synonyms":[{"name":"NRAS Noonan syndrome","type":"exact"},{"name":"NRAS gene related Noonan syndrome","type":"related"},{"name":"NS6","type":"exact"},{"name":"Noonan syndrome 6","type":"exact"},{"name":"Noonan syndrome caused by mutation in NRAS","type":"exact"},{"name":"Noonan syndrome type 6","type":"exact"}],"termid":"MONDO:0013186","terms_by_termid":{"MONDO:0013186":null},"xrefs":{"Monarch":{"xref_id":"0013186"}}}


id: PBO:0077866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomyosin 3 pseudogene 7","termid":"PBO:0077866"}


id: PR:Q10484
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- scs22 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10484"],"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 C17C9.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17C9.12","synonyms":[{"name":"Spom972h-scs22","type":"exact"}],"termid":"PR:Q10484"}


id: PBO:0028952
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-curved_cell_during_recovery_from_stationary_phase","termid":"PBO:0028952"}


id: PBO:0091391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic protein, human HAPSTR1 ortholog, stress response protein","termid":"PBO:0091391"}


id: PBO:0082315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Assembly factor that couples heme a synthesis to complex IV assembly; regulates the oligomerization state of the Cox15p heme a synthase, and couples this to the assembly of the cytochrome C oxidase complex (complex IV)","termid":"PBO:0082315"}


id: PBO:0036152
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_iMTOC","termid":"PBO:0036152"}


id: FYPO:0001617
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 L-isoleucine measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular amino acid level","termid":"FYPO:0003985"}],"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:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased cellular isoleucine level","synonyms":[{"name":"decreased cellular L-isoleucine level","type":"exact"},{"name":"decreased cellular isoleucine level during mitotic cell cycle","type":"related"},{"name":"decreased cellular isoleucine level during vegetative growth","type":"exact"},{"name":"decreased level of isoleucine in cell","type":"exact"},{"name":"reduced cellular isoleucine level","type":"exact"},{"name":"reduced level of isoleucine in cell","type":"exact"}],"termid":"FYPO:0001617"}


id: PBO:0027900
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_calcium_import","termid":"PBO:0027900"}


id: PBO:0065545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostaglandin D2 receptor 2","termid":"PBO:0065545"}


id: GO:0006851
data:
  {"annotated_genes":["SJAG_03399","SJAG_03873"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95135,96857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036444"}]},"cv_name":"biological_process","definition":"The process in which a calcium ion (Ca2+) is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium ion transmembrane transport","termid":"GO:0070588"},{"relation_name":"is_a","term_name":"mitochondrial transmembrane transport","termid":"GO:1990542"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03399":null,"SJAG_03873":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:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"mitochondrial calcium ion transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-8949215"],"synonyms":[{"name":"mitochondrial calcium transport","type":"exact"}],"termid":"GO:0006851","terms_by_termid":{"GO:0036444":null}}


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


id: PBO:0062345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily K member 4 pseudogene","termid":"PBO:0062345"}


id: PBO:0111860
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calponin homology (CH) domain","termid":"PBO:0111860"}


id: PR:O14307
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tRNA (adenine-N(1)-)-methyltransferase catalytic subunit TRMT61A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00817","PANTHER:PTHR12133:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit trm61 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9G1.12","secondary_identifiers":["UniProtKB:O14307"],"synonyms":[{"name":"Spom972h-TRMT61A","type":"exact"},{"name":"tRNA(m1A58)-methyltransferase subunit trm61 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tRNA(m1A58)MTase subunit trm61 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14307"}


id: GO:1902226
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of macrophage colony-stimulating factor signaling pathway.","definition_xrefs":["GOC:TermGenie","PMID:16705167"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine-mediated signaling pathway","termid":"GO:0001959"},{"relation_name":"is_a","term_name":"regulation of cellular response to macrophage colony-stimulating factor stimulus","termid":"GO:1903972"},{"relation_name":"regulates","term_name":"macrophage colony-stimulating factor signaling pathway","termid":"GO:0038145"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of macrophage colony-stimulating factor signaling pathway","synonyms":[{"name":"regulation of M-CSF signaling pathway","type":"exact"},{"name":"regulation of macrophage colony-stimulating factor signalling pathway","type":"exact"}],"termid":"GO:1902226"}


id: FYPO:0004252
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which regulation of DNA replication is normal (i.e. indistinguishable from wild type) when one or more replication forks arrest.","definition_xrefs":["PMID:24806966","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal regulation of DNA replication","termid":"FYPO:0002995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal regulation of DNA replication during replication fork arrest","synonyms":[{"name":"normal regulation of DNA replication during replication fork arrest during mitotic cell cycle","type":"exact"},{"name":"normal regulation of DNA replication during replication fork arrest during vegetative growth","type":"exact"},{"name":"normal regulation of nuclear cell cycle DNA replication during replication fork arrest","type":"exact"}],"termid":"FYPO:0004252"}


id: PBO:0043284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 4 member G pseudogene 1","termid":"PBO:0043284"}


id: GO:0098563
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the synaptic vesicle membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of synaptic vesicle membrane (obsolete GO:0098563)","termid":"GO:0098563"}


id: PBO:0040650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 binding component 3","termid":"PBO:0040650"}


id: MONDO:0018342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Joubert syndrome with Jeune asphyxiating thoracic dystrophy (JATD) is an extremely rare genetic bone disorder characterized by the classic features of Joubert syndrome (i.e. malformation of the brainstem causing ataxia, hypotonia,cognitive impairment, and abnormal eyemovements), associated with the skeletal anomalies found in JATD including short-rib dysplasia and narrow thorax causing respiratory failure, short limbs, and metaphyseal changes.","definition_xrefs":["Orphanet:397715"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome and related disorders","termid":"MONDO:0015369"},{"relation_name":"is_a","term_name":"short rib-polydactyly syndrome","termid":"MONDO:0015461"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Joubert syndrome with Jeune asphyxiating thoracic dystrophy","secondary_identifiers":["MEDGEN:1371401","SCTID:733418003","UMLS:C4518774","GARD:17637"],"synonyms":[{"name":"JBTS with JATD","type":"exact"},{"name":"Joubert syndrome with JATD","type":"exact"}],"termid":"MONDO:0018342","xrefs":{"Monarch":{"xref_id":"0018342"}}}


id: FYPO:0007877
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A gene expression phenotype observed in the vegetative growth phase of the life cycle in which regulation of translation in response to a chemical stimulus is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:34296454","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation regulation phenotype during vegetative growth","termid":"FYPO:0005044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal regulation of translation in response to chemical","synonyms":[{"name":"normal regulation of translation in response to chemical during mitotic cell cycle","type":"related"},{"name":"normal regulation of translation in response to chemical during vegetative growth","type":"exact"},{"name":"normal regulation of translation in response to chemical stimulus","type":"exact"},{"name":"normal translational regulation in response to chemical","type":"exact"}],"termid":"FYPO:0007877"}


id: MONDO:0859240
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":"intellectual developmental disorder with or without peripheral neuropathy","secondary_identifiers":["OMIM:619844","UMLS:C5676969","MEDGEN:1807523"],"termid":"MONDO:0859240","xrefs":{"Monarch":{"xref_id":"0859240"}}}


id: GO:0061738
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The autophagy process by which cytosolic proteins targeted for degradation are tagged with a chaperone and are directly transferred into and degraded in a late endosomal compartment.","definition_xrefs":["PMID:21238931","GOC:dph","GOC:autophagy","GOC:pad","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microautophagy","termid":"GO:0016237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006914","GO:0008150"],"is_obsolete":false,"name":"late endosomal microautophagy","secondary_identifiers":["Reactome:R-HSA-9615710"],"termid":"GO:0061738"}


id: PBO:0079633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2Q2 pseudogene 4, Y-linked","termid":"PBO:0079633"}


id: PBO:0041880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CATIP antisense RNA 2","termid":"PBO:0041880"}


id: GO:0014918
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which pressure natriuresis increases rate of natriuresis.","definition_xrefs":["GOC:mtg_cardio"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of natriuresis by pressure natriuresis (obsolete GO:0014918)","synonyms":[{"name":"positive regulation of natriuresis by pressure natriuresis","type":"exact"}],"termid":"GO:0014918"}


id: GO:0006424
data:
  {"annotated_genes":["SJAG_03071","SJAG_03277"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89835,100947],"is_not":false,"summary":null,"term":"GO:0006424"}]},"cv_name":"biological_process","definition":"The process of coupling glutamate to glutamyl-tRNA, catalyzed by glutamyl-tRNA synthetase. The glutamyl-tRNA synthetase is a class-I synthetase. The activated amino acid is transferred to the 2'-OH group of a glutamic acid-accetping tRNA. The 2'-O-aminoacyl-tRNA will ultimately migrate to the 3' position via transesterification.","definition_xrefs":["GOC:mcc","ISBN:0716730510"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA aminoacylation for protein translation","termid":"GO:0006418"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03071":null,"SJAG_03277":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0006399","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"glutamyl-tRNA aminoacylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0006424","terms_by_termid":{"GO:0006424":null}}


id: PBO:0061378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 38","termid":"PBO:0061378"}


id: GO:0001011
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to a specific DNA sequence and recruiting RNA polymerase to the DNA in order to form the preinitiation complex (PIC).","definition_xrefs":["GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription factor activity, sequence-specific DNA binding, RNA polymerase recruiting (obsolete GO:0001011)","synonyms":[{"name":"sequence-specific DNA binding RNA polymerase recruiting transcription factor activity","type":"exact"}],"termid":"GO:0001011"}


id: MONDO:0017157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary hypertension","termid":"MONDO:0005149"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary hypertension owing to lung disease and/or hypoxia","secondary_identifiers":["MEDGEN:785400","UMLS:C3698136","SCTID:697910001","ICD9:416.8","Orphanet:275837","GARD:21034"],"synonyms":[{"name":"PH due to lung disease and/or hypoxia","type":"exact"},{"name":"PH owing to lung disease and/or hypoxia","type":"exact"},{"name":"pulmonary hypertension due to lung disease and/or hypoxia","type":"exact"}],"termid":"MONDO:0017157","xrefs":{"Monarch":{"xref_id":"0017157"}}}


id: PBO:0089522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"steroid reductase","termid":"PBO:0089522"}


id: MONDO:0017803
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"}],"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":"primary progressive apraxia of speech","secondary_identifiers":["Orphanet:314566","UMLS:C5848171","GARD:21377","MEDGEN:1845725"],"synonyms":[{"name":"PPAOS","type":"exact"}],"termid":"MONDO:0017803","xrefs":{"Monarch":{"xref_id":"0017803"}}}


id: GO:0046257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of 2,4,6-trinitrotoluene, 1-methyl-2,4,6-trinitrobenzene, a highly explosive pale yellow crystalline solid, in the absence of oxygen.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete anaerobic 2,4,6-trinitrotoluene biosynthetic process (obsolete GO:0046257)","synonyms":[{"name":"anaerobic 2,4,6-trinitrotoluene anabolism","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene biosynthesis","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene biosynthetic process","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene formation","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene synthesis","type":"exact"}],"termid":"GO:0046257"}


id: MONDO:0012657
data:
  {"annotated_genes":["SJAG_01067"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85019],"is_not":false,"summary":null,"term":"MONDO:0012657"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01067":null},"genotype_count":0,"is_obsolete":false,"name":"Mungan syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1969653","MESH:C548078","MEDGEN:369554","OMIM:611376"],"synonyms":[{"name":"MGS","type":"exact"},{"name":"MUNGAN syndrome","type":"exact"},{"name":"pseudoobstruction chronic idiopathic intestinal with Barrett esophagus and cardiac abnormalities","type":"related"},{"name":"pseudoobstruction chronic idiopathic intestinal with Barrett oesophagus and cardiac abnormalities","type":"related"},{"name":"pseudoobstruction, chronic idiopathic intestinal, with Barrett esophagus and Cardiac abnormalities","type":"related"},{"name":"pseudoobstruction, chronic idiopathic intestinal, with Barrett oesophagus and Cardiac abnormalities","type":"related"},{"name":"visceral Neuromyopathy, familial, with pseudoobstruction, Megaduodenum, Barrett esophagus, and Cardiac abnormalities","type":"related"},{"name":"visceral neuromyopathy familial with pseudoobstruction megaduodenum Barrett esophagus and cardiac abnormalities","type":"related"},{"name":"visceral neuromyopathy familial with pseudoobstruction megaduodenum Barrett oesophagus and cardiac abnormalities","type":"related"}],"termid":"MONDO:0012657","terms_by_termid":{"MONDO:0012657":null},"xrefs":{"Monarch":{"xref_id":"0012657"}}}


id: PBO:0011123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanyl-nucleotide exchange factor Syt22","termid":"PBO:0011123"}


id: PBO:0003358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase (class I) Clr6","termid":"PBO:0003358"}


id: PBO:0041828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CART prepropeptide","termid":"PBO:0041828"}


id: PBO:0058349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4722","termid":"PBO:0058349"}


id: PBO:0064710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 46","termid":"PBO:0064710"}


id: GO:0102278
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: n H2O + chitin = N,N'-diacetylchitobiose.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete N,N'-diacetylchitobiose synthase activity (obsolete GO:0102278)","termid":"GO:0102278"}


id: PR:Q9C1W3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A squalene monooxygenase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02630","PANTHER:PTHR10835:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"squalene monooxygenase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC713.12","secondary_identifiers":["UniProtKB:Q9C1W3"],"synonyms":[{"name":"SE (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SQLE","type":"exact"},{"name":"squalene epoxidase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9C1W3"}


id: MONDO:0022946
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":"deafness progressive cataract autosomal dominant","termid":"MONDO:0022946","xrefs":{"Monarch":{"xref_id":"0022946"}}}


id: PBO:0044546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"death associated protein 3","termid":"PBO:0044546"}


id: GO:1905836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a triterpenoid stimulus.","definition_xrefs":["GOC:TermGenie","PMID:28078994","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"}],"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 triterpenoid","termid":"GO:1905836"}


id: PBO:0113456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of mitochondrial NAD(+)-dependent isocitrate dehydrogenase; complex catalyzes oxidation of isocitrate to alpha-ketoglutarate in TCA cycle; targeted to vacuole via AP-3 pathway","termid":"PBO:0113456"}


id: PBO:0046976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAM86B2 divergent transcript","termid":"PBO:0046976"}


id: PR:Q9UT33
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DPH3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR21454:SF2","OMA:SCHPO01198","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":"diphthamide biosynthesis protein 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8F11.02c","secondary_identifiers":["UniProtKB:Q9UT33"],"synonyms":[{"name":"Spom972h-DPH3","type":"exact"}],"termid":"PR:Q9UT33"}


id: PBO:0027759
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mislocalized_protein_during_meiotic_cell_cycle","termid":"PBO:0027759"}


id: PBO:0072958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCEL antisense RNA 1","termid":"PBO:0072958"}


id: PBO:0011091
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catabolism of ARginine, after cerevisiae","termid":"PBO:0011091"}


id: PBO:0034464
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-protein_mislocalized_to_vacuole","termid":"PBO:0034464"}


id: GO:0051685
data:
  {"annotated_genes":["SJAG_01116","SJAG_00053","SJAG_04221","SJAG_03170"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89922,103859],"is_not":false,"summary":null,"term":"GO:0051685"},{"annotations":[106493,114647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990854"}]},"cv_name":"biological_process","definition":"Any process in which the endoplasmic reticulum is maintained in a specific location within a cell and prevented from moving elsewhere.","definition_xrefs":["GOC:ai","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum localization","termid":"GO:0051643"},{"relation_name":"is_a","term_name":"maintenance of organelle location","termid":"GO:0051657"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_01116":null,"SJAG_03170":null,"SJAG_04221":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:0008150","GO:0051179"],"is_obsolete":false,"name":"maintenance of ER location","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"maintenance of ER localization","type":"related"},{"name":"maintenance of endoplasmic reticulum localization","type":"exact"}],"termid":"GO:0051685","terms_by_termid":{"GO:0051685":null,"GO:1990854":null}}


id: MONDO:0012722
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":"Dauwerse-Peters syndrome","secondary_identifiers":["MEDGEN:382037","MESH:C567093","UMLS:C2673203","OMIM:611733"],"synonyms":[{"name":"Dauwerse-Peters syndrome","type":"exact"},{"name":"short stature, Facial Dysmorphism, Severe brachydactyly, and syndactyly","type":"related"},{"name":"short stature, facial dysmorphism, severe brachydactyly and syndactyly","type":"related"}],"termid":"MONDO:0012722","xrefs":{"Monarch":{"xref_id":"0012722"}}}


id: PBO:0068040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 345","termid":"PBO:0068040"}


id: PBO:0003643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin Act1","termid":"PBO:0003643"}


id: MONDO:0035426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disorder potentially indicated for transplant or complication after transplantation (obsolete MONDO:0035426)","secondary_identifiers":["Orphanet:565779"],"termid":"MONDO:0035426","xrefs":{"Monarch":{"xref_id":"0035426"}}}


id: GO:0015936
data:
  {"annotated_genes":["SJAG_05277","SJAG_02247","SJAG_04627","SJAG_04288","SJAG_00427","SJAG_01139"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110054,88888,114282,116494,91731],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015937"},{"annotations":[99341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015938"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving coenzyme A, 3'-phosphoadenosine-(5')diphospho(4')pantatheine, an acyl carrier in many acylation and acyl-transfer reactions in which the intermediate is a thiol ester.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside phosphate metabolic process","termid":"GO:0006753"},{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"},{"relation_name":"is_a","term_name":"purine-containing compound metabolic process","termid":"GO:0072521"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00427":null,"SJAG_01139":null,"SJAG_02247":null,"SJAG_04288":null,"SJAG_04627":null,"SJAG_05277":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006790","GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"coenzyme A metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0006763"],"synonyms":[{"name":"CoA metabolism","type":"exact"},{"name":"coenzyme A metabolism","type":"exact"}],"termid":"GO:0015936","terms_by_termid":{"GO:0015937":null,"GO:0015938":null}}


id: PBO:0046224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin C pseudogene 17","termid":"PBO:0046224"}


id: GO:0150045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of synaptic signaling by nitric oxide.","definition_xrefs":["PMID:26311509","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication","termid":"GO:0010646"},{"relation_name":"is_a","term_name":"regulation of signaling","termid":"GO:0023051"},{"relation_name":"regulates","term_name":"synaptic signaling by nitric oxide","termid":"GO:0099163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of synaptic signaling by nitric oxide","termid":"GO:0150045"}


id: PBO:0083225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps with the uncharacterized ORF YGR068C","termid":"PBO:0083225"}


id: PBO:0089818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, MBF transcription factor complex subunit Cdc10","termid":"PBO:0089818"}


id: PBO:0004307
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"target of chaperonin-containing T-complex","termid":"PBO:0004307"}


id: MONDO:0006514
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Moderate to severe atopic dermatitis with allergic sensitisation.","definition_xrefs":["EFO:1000651"],"gene_count":0,"genotype_count":0,"name":"obsolete recalcitrant atopic dermatitis (obsolete MONDO:0006514)","secondary_identifiers":["PMID:25935106"],"termid":"MONDO:0006514","xrefs":{"Monarch":{"xref_id":"0006514"}}}


id: PBO:0004676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fumarylacetoacetate hydrolase family protein (predicted)","termid":"PBO:0004676"}


id: GO:0002142
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex of proteins that connect growing stereocilia in developing cochlear hair cells, composed of Vlgr1, usherin, vezatin, and whirlin.","definition_xrefs":["PMID:16775142"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"stereocilia ankle link","termid":"GO:0002141"}],"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":"stereocilia ankle link complex","termid":"GO:0002142"}


id: PBO:0068442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 16, pseudogene","termid":"PBO:0068442"}


id: PATO:0000532
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000532 micronutrient sensitivity value (obsolete PATO:0000532)","termid":"PATO:0000532"}


id: MONDO:0100116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A viral respiratory infection that is caused by the MERS coronavirus (MERS-CoV), which most often manifests with moderate to severe respiratory symptoms, including productive cough and shortness of breath, which can progress to pneumonia and acute respiratory distress syndrome.","definition_xrefs":["NCIT:C128424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"Orthocoronavirinae infectious disease","termid":"MONDO:0020753"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Middle East respiratory syndrome","secondary_identifiers":["GARD:22321","DOID:0080642","MEDGEN:811327","Orphanet:576074","UMLS:C3694279","icd11.foundation:1840423014"],"synonyms":[{"name":"MERS","type":"exact"},{"name":"camel flu","type":"exact"}],"termid":"MONDO:0100116","xrefs":{"Monarch":{"xref_id":"0100116"}}}


id: GO:0043386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a mycotoxin, any poisonous substance produced by a fungus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxin biosynthetic process","termid":"GO:0009403"},{"relation_name":"is_a","term_name":"mycotoxin metabolic process","termid":"GO:0043385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"mycotoxin biosynthetic process","synonyms":[{"name":"mycotoxin anabolism","type":"exact"},{"name":"mycotoxin biosynthesis","type":"exact"},{"name":"mycotoxin formation","type":"exact"},{"name":"mycotoxin synthesis","type":"exact"}],"termid":"GO:0043386"}


id: PBO:0082213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha 2 subunit of the 20S proteasome","termid":"PBO:0082213"}


id: PBO:0066150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBBP4 pseudogene 6","termid":"PBO:0066150"}


id: SO:0001011
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Peptide nucleic acid, is a chemical not known to occur naturally but is artificially synthesized and used in some biological research and medical treatments. The PNA backbone is composed of repeating N-(2-aminoethyl)-glycine units linked by peptide bonds. The purine and pyrimidine bases are linked to the backbone by methylene carbonyl bonds.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"PNA","termid":"SO:0001184"},{"relation_name":"is_a","term_name":"synthetic_oligo","termid":"SO:0001247"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PNA_oligo","secondary_identifiers":["http://en.wikipedia.org/wiki/Peptide_nucleic_acid"],"synonyms":[{"name":"PNA oligo","type":"exact"},{"name":"peptide nucleic acid","type":"exact"}],"termid":"SO:0001011"}


id: PBO:0018108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi to ER protein (predicted)","termid":"PBO:0018108"}


id: SO:0002080
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that intersects the exon of an incompletely annotated transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"incomplete_transcript_variant","termid":"SO:0002075"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"incomplete_transcript_exonic_variant","synonyms":[{"name":"incomplete transcript exonic variant","type":"exact"}],"termid":"SO:0002080"}


id: GO:0140793
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H2AX tyrosine phosphate (position 142) + H2O = histone H2AX tyrosine (position 142) + phosphate.","definition_xrefs":["PMID:19234442","PMID:19351884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone phosphatase activity","termid":"GO:0140789"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0004721"}],"interesting_parent_ids":["GO:0004721","GO:0003824","GO:0016788","GO:0016787","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"histone H2AXY142 phosphatase activity","synonyms":[{"name":"histone H2-Y142 phosphatase activity","type":"exact"},{"name":"histone H2Y142 phosphatase activity","type":"related"},{"name":"histone tyrosine phosphatase activity (H2-Y142 specific)","type":"exact"}],"termid":"GO:0140793"}


id: PBO:0068872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 112, pseudogene","termid":"PBO:0068872"}


id: SO:0001176
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Non-base-paired sequence of nucleotide bases in tRNA. It contains several dihydrouracil residues.","definition_xrefs":["ISBN:071671920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_region","termid":"SO:0001172"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DHU_loop","synonyms":[{"name":"D loop","type":"related"},{"name":"DHU loop","type":"exact"}],"termid":"SO:0001176"}


id: PBO:0013036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic protein, human CCDC174 ortholog","termid":"PBO:0013036"}


id: PBO:0043728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 6C pseudogene 7","termid":"PBO:0043728"}


id: GO:0006361
data:
  {"annotated_genes":["SJAG_01712","SJAG_02813","SJAG_01562","SJAG_05331","SJAG_02747","SJAG_03956","SJAG_00421","SJAG_00692","SJAG_00202","SJAG_04766","SJAG_01744"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90866,92678,94907,95080,107151,108611,109198,109241,111383,115894],"is_not":false,"summary":null,"term":"GO:0006361"},{"annotations":[95244,111382,108610,63536],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001188"}]},"cv_name":"biological_process","definition":"A transcription initiation process that takes place at a RNA polymerase I gene promoter. Ribosomal RNAs (rRNA) genes are transcribed by RNA polymerase I.","definition_xrefs":["GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription initiation","termid":"GO:0006352"},{"relation_name":"part_of","term_name":"transcription by RNA polymerase I","termid":"GO:0006360"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00202":null,"SJAG_00421":null,"SJAG_00692":null,"SJAG_01562":null,"SJAG_01712":null,"SJAG_01744":null,"SJAG_02747":null,"SJAG_02813":null,"SJAG_03956":null,"SJAG_04766":null,"SJAG_05331":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006351"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0006351","GO:0008150"],"is_obsolete":false,"name":"transcription initiation at RNA polymerase I promoter","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["Reactome:R-HSA-73854","GO:0001180"],"synonyms":[{"name":"transcription initiation from Pol I promoter","type":"exact"},{"name":"transcription initiation from RNA polymerase I promoter","type":"exact"},{"name":"transcription initiation from RNA polymerase I promoter for nuclear large rRNA transcript","type":"narrow"}],"termid":"GO:0006361","terms_by_termid":{"GO:0001188":null,"GO:0006361":null}}


id: PBO:0054048
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 1389","termid":"PBO:0054048"}


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


id: MONDO:0007031
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of abdominal aortic aneurysm that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"abdominal aortic aneurysm","termid":"MONDO:0005350"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial abdominal aortic aneurysm","secondary_identifiers":["SCTID:715364001","UMLS:C4275172","GARD:9181","icd11.foundation:556590106","MEDGEN:896628","OMIMPS:100070","Orphanet:86"],"synonyms":[{"name":"aortic aneurysm, familial abdominal","type":"exact"},{"name":"hereditary abdominal aortic aneurysm","type":"exact"}],"termid":"MONDO:0007031","xrefs":{"Monarch":{"xref_id":"0007031"}}}


id: PBO:0074286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLIT and NTRK like family member 1","termid":"PBO:0074286"}


id: PBO:0077512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 230","termid":"PBO:0077512"}


id: PBO:0066726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 23","termid":"PBO:0066726"}


id: GO:1904311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a gold(3+) stimulus.","definition_xrefs":["GOC:TermGenie","PMID:16206274","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to gold(3+)","termid":"GO:1904311"}


id: GO:0035398
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Positive regulation of a T cell mediated immune response mediated via cytokine production by a helper T cell.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of T cell mediated immunity","termid":"GO:0002711"},{"relation_name":"is_a","term_name":"helper T cell enhancement of adaptive immune response","termid":"GO:0035397"}],"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":"helper T cell enhancement of T cell mediated immune response","synonyms":[{"name":"helper T cell enhancement of T cell mediated immunity","type":"exact"},{"name":"provision of T cell help to T cell","type":"exact"}],"termid":"GO:0035398"}


id: SO:0001385
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A post translationally modified amino acid feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_amino_acid_feature","synonyms":[{"name":"modified amino acid feature","type":"exact"}],"termid":"SO:0001385"}


id: MONDO:0001937
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete LEOPARD syndrome (obsolete MONDO:0001937)","termid":"MONDO:0001937","xrefs":{"Monarch":{"xref_id":"0001937"}}}


id: MONDO:1012297
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hymen, imperforate, non-human animal","termid":"MONDO:1010279"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"imperforate hymen, cattle","secondary_identifiers":["OMIA:001107-9913"],"termid":"MONDO:1012297","xrefs":{"Monarch":{"xref_id":"1012297"}}}


id: FYPO:0007727
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of late endosomes is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal endomembrane system morphology","termid":"FYPO:0000353"}],"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":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal late endosome morphology","synonyms":[{"name":"abnormal PVE morphology","type":"exact"},{"name":"abnormal late endosome morphology during mitotic cell cycle","type":"related"},{"name":"abnormal late endosome morphology during vegetative growth","type":"exact"},{"name":"abnormal prevacuolar compartment morphology","type":"exact"},{"name":"abnormal prevacuolar endosome morphology","type":"exact"}],"termid":"FYPO:0007727"}


id: PBO:0048330
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 41","termid":"PBO:0048330"}


id: MONDO:0010936
data:
  {"annotated_genes":["SJAG_04489"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84853],"is_not":false,"summary":null,"term":"MONDO:0010936"}]},"cv_name":"mondo","definition":"Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the CHMP2B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"},{"relation_name":"is_a","term_name":"behavioral variant of frontotemporal dementia","termid":"MONDO:0017160"},{"relation_name":"is_a","term_name":"frontotemporal dementia and/or amyotrophic lateral sclerosis","termid":"MONDO:0030923"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04489":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"frontotemporal dementia and/or amyotrophic lateral sclerosis 7","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:331.19","SCTID:702393003","DOID:0111227","MESH:C579991","GARD:15322","OMIM:614696","UMLS:C1833296","MEDGEN:318833","DOID:0060208","MESH:C563708","OMIM:600795"],"synonyms":[{"name":"CHMP2B amyotrophic lateral sclerosis","type":"exact"},{"name":"CHMP2B-related amyotrophic lateral sclerosis","type":"exact"},{"name":"Dmt1","type":"related"},{"name":"FTD3","type":"exact"},{"name":"amyotrophic lateral sclerosis caused by mutation in CHMP2B","type":"exact"},{"name":"amyotrophic lateral sclerosis, Chmp2B-related","type":"exact"},{"name":"dementia, familial nonspecific","type":"related"},{"name":"frontotemporal dementia, chromosome 3-linked","type":"exact"}],"termid":"MONDO:0010936","terms_by_termid":{"MONDO:0010936":null},"xrefs":{"Monarch":{"xref_id":"0010936"}}}


id: PBO:0108542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A)site selection protein Seb1","termid":"PBO:0108542"}


id: PBO:0044652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynactin subunit 3","termid":"PBO:0044652"}


id: PBO:0062732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily B member 6","termid":"PBO:0062732"}


id: GO:0080048
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GDP-alpha-D-glucose + phosphate = alpha-D-glucose-1-phosphate + GDP.","definition_xrefs":["PMID:17462988","PMID:18463094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanylyltransferase activity","termid":"GO:0070568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016779","GO:0003824"],"is_obsolete":false,"name":"GDP-D-glucose phosphorylase activity","secondary_identifiers":["MetaCyc:RXN-12486","EC:2.7.7.78","RHEA:30387","GO:0010474"],"synonyms":[{"name":"GDP:glucose-1-phosphate guanyltransferase activity","type":"exact"},{"name":"glucose-1-phosphate guanylyltransferase (GDP) activity","type":"exact"}],"termid":"GO:0080048"}


id: MONDO:0002151
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dysostosis (obsolete MONDO:0002151)","termid":"MONDO:0002151","xrefs":{"Monarch":{"xref_id":"0002151"}}}


id: FYPO:0005018
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of double-stranded DNA binding by a gene product is decreased, when a gene or the bound DNA sequence is mutated. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased DNA binding","termid":"FYPO:0000658"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000653"}],"interesting_parent_ids":["FYPO:0000653","FYPO:0000652","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"decreased double-stranded DNA binding","synonyms":[{"name":"decreased dsDNA binding","type":"exact"},{"name":"reduced double-stranded DNA binding","type":"exact"}],"termid":"FYPO:0005018"}


id: GO:0072721
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a dithiothreitol stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to dithiothreitol","termid":"GO:0072720"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to dithiothreitol","synonyms":[{"name":"cellular response to 1,4-dithiothreitol","type":"exact"},{"name":"cellular response to DTT","type":"exact"}],"termid":"GO:0072721"}


id: PBO:0047241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 236 member A","termid":"PBO:0047241"}


id: PATO:0000139
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000139 relative orientation (obsolete PATO:0000139)","termid":"PATO:0000139"}


id: PBO:0045505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dentin sialophosphoprotein","termid":"PBO:0045505"}


id: GO:0021871
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process resulting in the creation of areas within the forebrain that will direct the behavior of cell migration in differentiation as the forebrain develops.","definition_xrefs":["GO_REF:0000021","GOC:cls","GOC:dph","GOC:jid","GOC:dgh","GOC:isa_complete","PMID:16226447"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"part_of","term_name":"forebrain development","termid":"GO:0030900"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"forebrain regionalization","termid":"GO:0021871"}


id: PBO:0071540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 5","termid":"PBO:0071540"}


id: GO:0050932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of pigmented cell differentiation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell differentiation","termid":"GO:0045595"},{"relation_name":"regulates","term_name":"pigment cell differentiation","termid":"GO:0050931"}],"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 pigment cell differentiation","termid":"GO:0050932"}


id: PBO:0060265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYG1 antisense RNA 1","termid":"PBO:0060265"}


id: GO:0009075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving amino acids of the histidine family.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete histidine family amino acid metabolic process (obsolete GO:0009075)","synonyms":[{"name":"histidine family amino acid metabolic process","type":"exact"},{"name":"histidine family amino acid metabolism","type":"exact"}],"termid":"GO:0009075"}


id: GO:0100064
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that negatively regulates filamentous growth of a population of unicellular organisms in response to starvation.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of filamentous growth of a population of unicellular organisms in response to starvation by transcription from RNA polymerase II promoter (obsolete GO:0100064)","termid":"GO:0100064"}


id: GO:0071521
data:
  {"annotated_genes":["SJAG_00514","SJAG_00845","SJAG_04509","SJAG_01794","SJAG_00596","SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87389,89361,90345,92971,103175,104006],"is_not":false,"summary":null,"term":"GO:0071521"}]},"cv_name":"cellular_component","definition":"A protein complex formed by the association of the small GTPase Cdc42 with additional proteins. In Schizosaccharomyces the complex contains the Cdc42, Ras1, Scd1, Scd2, andShk1 proteins, and functions in the Ras1-Scd GTPase signaling pathway.","definition_xrefs":["PMID:7923372","PMID:8943016","GOC:mah","PMID:10567532","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"GTPase complex","termid":"GO:1905360"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_00596":null,"SJAG_00845":null,"SJAG_01794":null,"SJAG_03453":null,"SJAG_04509":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"Cdc42 GTPase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Ras1-Scd1-Scd2-Cdc42-Shk1 complex","type":"exact"}],"termid":"GO:0071521","terms_by_termid":{"GO:0071521":null}}


id: PBO:0027814
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-lagging_chromosomes_during_meiosis_I","termid":"PBO:0027814"}


id: PBO:0083826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential subunit of the Pan2p-Pan3p poly(A)-ribonuclease complex; poly (A) mRNA binding subunit which recruits mRNA to the complex; the Pan2p-Pan3p complex controls poly(A) tail length and regulates the stoichiometry and activity of postreplication repair complexes","termid":"PBO:0083826"}


id: PATO:0001055
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An angular placement quality inhering in a bearer by virtue of the bearer's placement at an angle that is greater than 180 degrees but less than 360 degrees to another entity.","definition_xrefs":["thesaurus.maths:thesaurus.maths"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angle","termid":"PATO:0002326"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reflex angle to","termid":"PATO:0001055"}


id: GO:0033986
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a methanol stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to alcohol","termid":"GO:0097305"}],"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 methanol","termid":"GO:0033986"}


id: SO:0001915
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region defined by a cluster of experimentally determined transcription starting sites.","definition_xrefs":["PMID:21372179","SO:andrewgibson","PMID:19624849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"experimental_feature","termid":"SO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription_start_cluster","synonyms":[{"name":"TSC","type":"exact"},{"name":"TSS cluster","type":"exact"},{"name":"transcriptional initiation cluster","type":"exact"},{"name":"transcriptional start site cluster","type":"exact"}],"termid":"SO:0001915"}


id: PBO:0030315
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_myristoyl-CoA_ligase_activity","termid":"PBO:0030315"}


id: PBO:0111876
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-CSL","termid":"PBO:0111876"}


id: PBO:0079347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 31, pseudogene","termid":"PBO:0079347"}


id: MONDO:0009662
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mucopolysaccharidosis type VII (MPS VII) is a very rare lysosomal storage disease belonging to the group of mucopolysaccharidoses.","definition_xrefs":["Orphanet:584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis","termid":"MONDO:0019249"},{"relation_name":"is_a","term_name":"lysosomal storage disease with skeletal involvement","termid":"MONDO:0800088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561","MONDO:0037792"],"is_obsolete":false,"name":"mucopolysaccharidosis type 7","secondary_identifiers":["UMLS:C0085132","NANDO:1200111","DOID:12803","MEDGEN:43108","icd11.foundation:1563668250","NCIT:C84903","MedDRA:10056893","OMIM:253220","GARD:7096","MESH:D016538","SCTID:43916004","NANDO:2200552","NORD:1722"],"synonyms":[{"name":"Beta-glucuronidase deficiency","type":"exact"},{"name":"Gus deficiency","type":"related"},{"name":"Gusb deficiency","type":"related"},{"name":"MPS 7","type":"related"},{"name":"MPS VII","type":"related"},{"name":"MPS VII - Sly syndrome","type":"exact"},{"name":"MPS VII - mucopolysaccharidosis VII","type":"related"},{"name":"MPS7","type":"exact"},{"name":"MPSVII","type":"exact"},{"name":"Mucopolysaccharidosis Type VII","type":"exact"},{"name":"Sly disease","type":"exact"},{"name":"Sly syndrome","type":"exact"},{"name":"beta-glucuronidase deficiency","type":"exact"},{"name":"deficiency of beta-glucuronidase","type":"exact"},{"name":"gusb deficiency","type":"related"},{"name":"mucopolysaccharidosis VII","type":"exact"},{"name":"mucopolysaccharidosis type 7","type":"exact"},{"name":"mucopolysaccharidosis type VII","type":"exact"},{"name":"mucopolysaccharidosis, mps-VII","type":"exact"},{"name":"mucopolysaccharidosis, type 7","type":"related"},{"name":"mucopolysaccharidosis, type VII","type":"related"}],"termid":"MONDO:0009662","xrefs":{"Monarch":{"xref_id":"0009662"}}}


id: PBO:0080839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y-box binding protein 1 pseudogene 3","termid":"PBO:0080839"}


id: PBO:0076483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TARBP2 subunit of RISC loading complex","termid":"PBO:0076483"}


id: GO:0047636
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,2'-iminodipropanoate + H2O + NAD+ = L-alanine + H+ + NADH + pyruvate.","definition_xrefs":["EC:1.5.1.17","RHEA:17589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"alanopine dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R00398","MetaCyc:ALANOPINE-DEHYDROGENASE-RXN"],"synonyms":[{"name":"2,2'-iminodipropanoate:NAD+ oxidoreductase (L-alanine-forming)","type":"related"},{"name":"ADH","type":"related"},{"name":"ALPDH","type":"related"},{"name":"alanopine: NAD oxidoreductase activity","type":"related"},{"name":"alanopine:NAD oxidoreductase activity","type":"related"},{"name":"alanopine[meso-N-(1-carboxyethyl)-alanine]dehydrogenase activity","type":"related"},{"name":"meso-N-(1-carboxyethyl)-alanine:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0047636"}


id: PBO:0080637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 86","termid":"PBO:0080637"}


id: PBO:0110360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENR pseudogene 4","termid":"PBO:0110360"}


id: MONDO:0024889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign epithelial neoplasm of the female reproductive system arising from mesonephric remnants.","definition_xrefs":["NCIT:C4294"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"benign reproductive system neoplasm","termid":"MONDO:0000383"},{"relation_name":"is_a","term_name":"kidney benign neoplasm","termid":"MONDO:0002513"},{"relation_name":"is_a","term_name":"mesonephric neoplasm","termid":"MONDO:0024888"},{"relation_name":"is_a","term_name":"benign epithelial neoplasm","termid":"MONDO:0036976"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"benign mesonephroma","secondary_identifiers":["ICDO:9110/0","DOID:2616","MEDGEN:87259","UMLS:C0334530"],"synonyms":[{"name":"Mesonephroma, benign","type":"exact"},{"name":"Mesonephroma, benign (morphologic abnormality)","type":"exact"},{"name":"Wolffian duct adenoma","type":"exact"},{"name":"benign Mesonephroma","type":"exact"},{"name":"benign mesonephric neoplasm","type":"exact"},{"name":"mesonephric adenoma","type":"exact"},{"name":"mesonephric duct adenoma","type":"exact"},{"name":"mesonephric neoplasm, benign","type":"exact"}],"termid":"MONDO:0024889","xrefs":{"Monarch":{"xref_id":"0024889"}}}


id: PBO:0085584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in apoptosis; variously described as containing a BCL-2 homology (BH3) domain or as a member of the BAX inhibitor family; reported to promote apoptosis under some conditions and to inhibit it in others; localizes to ER and vacuole; may link the unfolded protein response to apoptosis via regulation of calcium-mediated signaling; translocates to mitochondria under apoptosis-inducing conditions in a process involving Mir1p and Cor1p","termid":"PBO:0085584"}


id: GO:0016332
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any cellular process that results in the specification, formation or maintenance of anisotropic intracellular organization of epithelial cells in an embryo.","definition_xrefs":["GOC:isa_complete","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment or maintenance of cell polarity","termid":"GO:0007163"},{"relation_name":"part_of","term_name":"morphogenesis of embryonic epithelium","termid":"GO:0016331"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"establishment or maintenance of polarity of embryonic epithelium","termid":"GO:0016332"}


id: SO:0000696
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A short oligonucleotide sequence, of length on the order of 10's of bases; either single or double stranded.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent","termid":"SO:0000695"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligo","secondary_identifiers":["http://en.wikipedia.org/wiki/Oligonucleotide"],"synonyms":[{"name":"oligonucleotide","type":"exact"}],"termid":"SO:0000696"}


id: MONDO:0013327
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary hyperoxaluria type 3 (PH3) is a disorder of glyoxylate metabolism that can be asymptomatic or characterized by oxalate nephrolithiasis.","definition_xrefs":["Orphanet:93600"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary hyperoxaluria","termid":"MONDO:0002474"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"primary hyperoxaluria type 3","secondary_identifiers":["UMLS:C3150878","GARD:10738","OMIM:613616","DOID:0111672","MEDGEN:462228","NCIT:C123214","SCTID:734990008"],"synonyms":[{"name":"HOGA1 primary hyperoxaluria","type":"exact"},{"name":"HP3","type":"related"},{"name":"PH III","type":"related"},{"name":"hyperoxaluria, primary, type 3","type":"related"},{"name":"hyperoxaluria, primary, type III","type":"related"},{"name":"primary hyperoxaluria caused by mutation in HOGA1","type":"exact"},{"name":"primary hyperoxaluria type III","type":"exact"}],"termid":"MONDO:0013327","xrefs":{"Monarch":{"xref_id":"0013327"}}}


id: PBO:0045803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"erythroid differentiation regulatory factor 1","termid":"PBO:0045803"}


id: PBO:0084311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Isomaltase (alpha-1,6-glucosidase/alpha-methylglucosidase); preferred specificity for isomaltose, alpha-methylglucoside, and palatinose, but also exhibits alpha-1,2 glucosidase activity on sucrose and kojibiose, and can cleave the 1,3-alpha linkage of nigerose and turanose and the alpha-1,5 linkage of leucrose in vitro; not required for isomaltose utilization, but Ima2p overexpression allows the ima1 null mutant to grow on isomaltose","termid":"PBO:0084311"}


id: MONDO:0011953
data:
  {"annotated_genes":["SJAG_02520"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86792],"is_not":false,"summary":null,"term":"MONDO:0011953"}]},"cv_name":"mondo","definition":"Familial acute necrotizing encephalopathy or ADANE is a potentially fatal neurological disease characterized by neuropathological lesions principally involving the brainstem, thalamus and putamen.","definition_xrefs":["Orphanet:88619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"encephalopathy, acute, infection-induced","termid":"MONDO:0000166"},{"relation_name":"is_a","term_name":"Mendelian encephalopathy","termid":"MONDO:0100198"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02520":null},"genotype_count":0,"is_obsolete":false,"name":"familial acute necrotizing encephalopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C2675556","GARD:13232","SCTID:723359002","MEDGEN:382634","OMIM:608033"],"synonyms":[{"name":"ADANE","type":"exact"},{"name":"ANE1","type":"related"},{"name":"IIAE3","type":"related"},{"name":"Postinfectious acute necrotizing hemorrhagic encephalopathy","type":"related"},{"name":"acute necrotizing encephalopathy type 1","type":"related"},{"name":"autosomal dominant acute necrotizing encephalopathy","type":"related"},{"name":"encephalopathy, acute necrotizing, susceptibility to","type":"related"},{"name":"encephalopathy, acute, infection-induced, 3, susceptibility to","type":"exact"},{"name":"encephalopathy, acute, infection-induced, susceptibility to, 3","type":"related"},{"name":"encephalopathy, acute, infection-induced, susceptibility to, type 3","type":"exact"},{"name":"infection-induced acute encephalopathy 3","type":"related"},{"name":"recurrent acute necrotizing encephalopathy","type":"exact"},{"name":"susceptibility to acute infection-induced encephalopathy-3","type":"related"},{"name":"susceptibility to acute necrotizing encephalopathy","type":"related"},{"name":"susceptibility to infection-induced acute encephalopathy 3","type":"related"}],"termid":"MONDO:0011953","terms_by_termid":{"MONDO:0011953":null},"xrefs":{"Monarch":{"xref_id":"0011953"}}}


id: GO:0009998
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that restricts, stops or prevents a cell from specifying into a retinal cone cell.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate specification","termid":"GO:0009996"},{"relation_name":"is_a","term_name":"regulation of retinal cone cell fate specification","termid":"GO:0042673"},{"relation_name":"is_a","term_name":"negative regulation of retinal cone cell fate commitment","termid":"GO:0060226"},{"relation_name":"negatively_regulates","term_name":"retinal cone cell fate specification","termid":"GO:0042672"}],"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 retinal cone cell fate specification","synonyms":[{"name":"down regulation of retinal cone cell fate specification","type":"exact"},{"name":"down-regulation of retinal cone cell fate specification","type":"exact"},{"name":"downregulation of retinal cone cell fate specification","type":"exact"},{"name":"inhibition of retinal cone cell fate specification","type":"narrow"},{"name":"negative regulation of retina cone cell fate specification","type":"exact"},{"name":"suppression of retina cone cell fate","type":"exact"},{"name":"suppression of retinal cone cell fate","type":"exact"}],"termid":"GO:0009998"}


id: PBO:0068953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 197, pseudogene","termid":"PBO:0068953"}


id: GO:0010199
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which boundaries between lateral organs and the meristem is established and maintained.","definition_xrefs":["PMID:12068116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formation of plant organ boundary","termid":"GO:0090691"}],"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":"organ boundary specification between lateral organs and the meristem","termid":"GO:0010199"}


id: GO:0050786
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a RAGE receptor, the receptor for advanced glycation end-products.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"RAGE receptor binding","synonyms":[{"name":"advanced glycation end-product receptor binding","type":"exact"}],"termid":"GO:0050786"}


id: GO:0052499
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete pathogen-associated molecular pattern dependent modulation by organism of symbiont innate immunity (obsolete GO:0052499)","synonyms":[{"name":"pathogen-associated molecular pattern dependent modulation by organism of symbiont innate immunity","type":"exact"}],"termid":"GO:0052499"}


id: PBO:0004600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin exportin T Los1 (predicted)","termid":"PBO:0004600"}


id: FYPO:0002876
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which transcription occurs to a lower extent than normal. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"decreased RNA level","termid":"FYPO:0000826"},{"relation_name":"is_a","term_name":"abnormal transcription","termid":"FYPO:0005502"},{"relation_name":"is_a","term_name":"decreased gene expression","termid":"FYPO:0006549"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0006551","FYPO:0000002","FYPO:0000294","FYPO:0005447"],"is_obsolete":false,"name":"decreased transcription","synonyms":[{"name":"reduced transcription","type":"exact"}],"termid":"FYPO:0002876"}


id: PBO:0029460
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-enlarged_nucleus","termid":"PBO:0029460"}


id: GO:0016755
data:
  {"annotated_genes":["SJAG_02319","SJAG_01772","SJAG_04857","SJAG_01535","SJAG_02299","SJAG_02521","SJAG_02575","SJAG_01900","SJAG_00475","SJAG_03112","SJAG_01360","SJAG_03387","SJAG_00604","SJAG_05022","SJAG_03968","SJAG_00435","SJAG_03883","SJAG_00188","SJAG_04689","SJAG_03136","SJAG_05274","SJAG_02347","SJAG_03006","SJAG_03175","SJAG_01593","SJAG_04915","SJAG_04151","SJAG_02918","SJAG_02169","SJAG_02308","SJAG_01637","SJAG_04516","SJAG_01018","SJAG_05340","SJAG_00300","SJAG_04966","SJAG_01679","SJAG_04573","SJAG_03613","SJAG_01992","SJAG_01507","SJAG_02851","SJAG_03618","SJAG_03615","SJAG_00111","SJAG_04990","SJAG_02082","SJAG_03005","SJAG_01253","SJAG_01776","SJAG_03860","SJAG_02685","SJAG_00931","SJAG_05323","SJAG_00509","SJAG_01212","SJAG_00552","SJAG_02746","SJAG_04309","SJAG_02705","SJAG_00727","SJAG_01165","SJAG_04783","SJAG_00500","SJAG_03831","SJAG_04600","SJAG_02652","SJAG_05264","SJAG_01413","SJAG_04619","SJAG_04612","SJAG_00208","SJAG_00293","SJAG_06309","SJAG_00341","SJAG_03657","SJAG_05236","SJAG_02415","SJAG_00903","SJAG_04429","SJAG_00209","SJAG_00855","SJAG_00819","SJAG_01561","SJAG_00173","SJAG_03970","SJAG_02668","SJAG_03636","SJAG_03191","SJAG_02603","SJAG_00561","SJAG_03250","SJAG_03324","SJAG_01533","SJAG_01251","SJAG_02371","SJAG_01854"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004057"},{"annotations":[92417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061651"},{"annotations":[109234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141046"},{"annotations":[89599,109235,109733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019776"},{"annotations":[108178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016603"},{"annotations":[96875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016756"},{"annotations":[118280,115657],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140850"},{"annotations":[93858],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140851"},{"annotations":[117829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061654"},{"annotations":[101425,98600,100587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000048"},{"annotations":[103962,95712],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061656"},{"annotations":[89112,89266,103843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061665"},{"annotations":[112430,90752,87686,87311,113715,87529,101467,107639,101602,105924,116229,101754],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061631"},{"annotations":[89406,90581,94896,93073,104712,93859,109428,87744,90244,92272,100679,91191,112838,116146,113767,89235,98895,88153,109427,102895,96019,96286,116685,102910,99749,89060,87828,79420,106338,113445,87609,117873,95316,103844,103773,111537,96204,96104,89303,87530,104431,87540,104769,105369,112263,106420,107334,104459,116147,89718,108338,116645,88853,88415,102511,98043,107470,109104,109690,114858,113015,100799,101361,113106],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061630"},{"annotations":[106661,113079,91017,104349],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061659"},{"annotations":[96888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004842"},{"annotations":[92207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034450"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of an amino-acyl group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity","termid":"GO:0016746"}],"gene_count":97,"genes_by_uniquename":{"SJAG_00111":null,"SJAG_00173":null,"SJAG_00188":null,"SJAG_00208":null,"SJAG_00209":null,"SJAG_00293":null,"SJAG_00300":null,"SJAG_00341":null,"SJAG_00435":null,"SJAG_00475":null,"SJAG_00500":null,"SJAG_00509":null,"SJAG_00552":null,"SJAG_00561":null,"SJAG_00604":null,"SJAG_00727":null,"SJAG_00819":null,"SJAG_00855":null,"SJAG_00903":null,"SJAG_00931":null,"SJAG_01018":null,"SJAG_01165":null,"SJAG_01212":null,"SJAG_01251":null,"SJAG_01253":null,"SJAG_01360":null,"SJAG_01413":null,"SJAG_01507":null,"SJAG_01533":null,"SJAG_01535":null,"SJAG_01561":null,"SJAG_01593":null,"SJAG_01637":null,"SJAG_01679":null,"SJAG_01772":null,"SJAG_01776":null,"SJAG_01854":null,"SJAG_01900":null,"SJAG_01992":null,"SJAG_02082":null,"SJAG_02169":null,"SJAG_02299":null,"SJAG_02308":null,"SJAG_02319":null,"SJAG_02347":null,"SJAG_02371":null,"SJAG_02415":null,"SJAG_02521":null,"SJAG_02575":null,"SJAG_02603":null,"SJAG_02652":null,"SJAG_02668":null,"SJAG_02685":null,"SJAG_02705":null,"SJAG_02746":null,"SJAG_02851":null,"SJAG_02918":null,"SJAG_03005":null,"SJAG_03006":null,"SJAG_03112":null,"SJAG_03136":null,"SJAG_03175":null,"SJAG_03191":null,"SJAG_03250":null,"SJAG_03324":null,"SJAG_03387":null,"SJAG_03613":null,"SJAG_03615":null,"SJAG_03618":null,"SJAG_03636":null,"SJAG_03657":null,"SJAG_03831":null,"SJAG_03860":null,"SJAG_03883":null,"SJAG_03968":null,"SJAG_03970":null,"SJAG_04151":null,"SJAG_04309":null,"SJAG_04429":null,"SJAG_04516":null,"SJAG_04573":null,"SJAG_04600":null,"SJAG_04612":null,"SJAG_04619":null,"SJAG_04689":null,"SJAG_04783":null,"SJAG_04857":null,"SJAG_04915":null,"SJAG_04966":null,"SJAG_04990":null,"SJAG_05022":null,"SJAG_05236":null,"SJAG_05264":null,"SJAG_05274":null,"SJAG_05323":null,"SJAG_05340":null,"SJAG_06309":null},"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"aminoacyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:2.3.2.-"],"synonyms":[{"name":"transferase activity, transferring amino-acyl groups","type":"exact"}],"termid":"GO:0016755","terms_by_termid":{"GO:0000048":null,"GO:0004057":null,"GO:0004842":null,"GO:0016603":null,"GO:0016756":null,"GO:0019776":null,"GO:0034450":null,"GO:0061630":null,"GO:0061631":null,"GO:0061651":null,"GO:0061654":null,"GO:0061656":null,"GO:0061659":null,"GO:0061665":null,"GO:0140850":null,"GO:0140851":null,"GO:0141046":null}}


id: PBO:0052139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel subfamily H member 6","termid":"PBO:0052139"}


id: PBO:0085470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Prephenate dehydrogenase involved in tyrosine biosynthesis; expression is dependent on phenylalanine levels","termid":"PBO:0085470"}


id: MONDO:0032656
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":"microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum","secondary_identifiers":["UMLS:C4748984","MEDGEN:1648355","OMIM:618284"],"synonyms":[{"name":"MCIDDS","type":"related"},{"name":"MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM","type":"related"}],"termid":"MONDO:0032656","xrefs":{"Monarch":{"xref_id":"0032656"}}}


id: MONDO:0003673
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An electrocardiographic finding of an injury in leads corresponding to the anatomic region of the apex of the heart.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myocardial infarction","termid":"MONDO:0005068"}],"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":"apical myocardial infarction","secondary_identifiers":["MEDGEN:770959","DOID:5848","UMLS:C3642319"],"termid":"MONDO:0003673","xrefs":{"Monarch":{"xref_id":"0003673"}}}


id: GO:0010477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a sulfur dioxide (SO2) stimulus.","definition_xrefs":["PMID:17425719"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"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 sulfur dioxide","termid":"GO:0010477"}


id: GO:0106345
data:
  {"annotated_genes":["SJAG_01432","SJAG_00281"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100522,104559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030267"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: glycolate + NAD(P)+ = glyoxylate + NAD(P)H.","definition_xrefs":["GOC:curators","PMID:3548703"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00281":null,"SJAG_01432":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"glyoxylate reductase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0106345","terms_by_termid":{"GO:0030267":null}}


id: GO:0043305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of mast cell degranulation.","definition_xrefs":["ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of myeloid leukocyte mediated immunity","termid":"GO:0002887"},{"relation_name":"is_a","term_name":"negative regulation of leukocyte degranulation","termid":"GO:0043301"},{"relation_name":"is_a","term_name":"regulation of mast cell degranulation","termid":"GO:0043304"},{"relation_name":"negatively_regulates","term_name":"mast cell degranulation","termid":"GO:0043303"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mast cell degranulation","synonyms":[{"name":"down regulation of mast cell degranulation","type":"exact"},{"name":"down-regulation of mast cell degranulation","type":"exact"},{"name":"downregulation of mast cell degranulation","type":"exact"},{"name":"inhibition of mast cell degranulation","type":"narrow"},{"name":"negative regulation of mast cell granule exocytosis","type":"exact"}],"termid":"GO:0043305"}


id: GO:0042386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the characteristics of a mature hemocyte. Hemocytes are blood cells associated with a hemocoel (the cavity containing most of the major organs of the arthropod body) which are involved in defense and clotting of hemolymph, but not involved in transport of oxygen.","definition_xrefs":["GOC:mtg_sensu","GOC:jl","CL:0000387","PMID:9550723"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system process","termid":"GO:0002376"},{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hemocyte differentiation","synonyms":[{"name":"arthropod blood cell differentiation","type":"exact"}],"termid":"GO:0042386"}


id: GO:0061581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a corneal epithelial cell from one site to another, often during the development of a multicellular organism.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell migration","termid":"GO:0010631"}],"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":"corneal epithelial cell migration","termid":"GO:0061581"}


id: FYPO:0004736
data:
  {"alleles_by_uniquename":{"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_04280:allele-1":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-1"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118780],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001369"}],"single_locus_phenotype":[{"annotations":[119002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002026"},{"annotations":[118781],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001369"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the position, composition or morphology of the actomyosin contractile ring is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cytoskeleton during vegetative growth","termid":"FYPO:0002398"},{"relation_name":"output_of","term_name":"abnormal actomyosin contractile ring organization","termid":"FYPO:0004738"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02392":null,"SJAG_04280":null,"SJAG_04522":null},"genotype_count":3,"genotypes_by_uniquename":{"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0004803","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000631"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04522","SJAG_04280"],"name":"abnormal actomyosin contractile ring","references_by_uniquename":{"PMID:25866389":null,"PMID:30664646":null},"single_locus_annotated_genes":["SJAG_02392","SJAG_04522"],"single_locus_genotype_uniquenames":["pom1delta","rga4delta"],"synonyms":[{"name":"abnormal actomyosin contractile ring during mitotic cell cycle","type":"related"},{"name":"abnormal actomyosin contractile ring during vegetative growth","type":"exact"},{"name":"abnormal contractile ring","type":"exact"},{"name":"abnormal cytokinetic contractile ring","type":"exact"},{"name":"abnormal mitotic contractile ring","type":"exact"}],"termid":"FYPO:0004736","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000338":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:1902548
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 vascular endothelial growth factor stimulus.","definition_xrefs":["GOC:rl","GOC:BHF","PMID:17895370","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular response to growth factor stimulus","termid":"GO:0090288"},{"relation_name":"is_a","term_name":"regulation of cellular response to vascular endothelial growth factor stimulus","termid":"GO:1902547"},{"relation_name":"negatively_regulates","term_name":"cellular response to vascular endothelial growth factor stimulus","termid":"GO:0035924"}],"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 vascular endothelial growth factor stimulus","synonyms":[{"name":"down regulation of cellular response to VEGF","type":"exact"},{"name":"down regulation of cellular response to VEGFA","type":"narrow"},{"name":"down regulation of cellular response to VEGFB","type":"narrow"},{"name":"down regulation of cellular response to vascular endothelial growth factor","type":"exact"},{"name":"down regulation of cellular response to vascular endothelial growth factor stimulus","type":"exact"},{"name":"down-regulation of cellular response to VEGF","type":"exact"},{"name":"down-regulation of cellular response to VEGFA","type":"narrow"},{"name":"down-regulation of cellular response to VEGFB","type":"narrow"},{"name":"down-regulation of cellular response to vascular endothelial growth factor","type":"exact"},{"name":"down-regulation of cellular response to vascular endothelial growth factor stimulus","type":"exact"},{"name":"downregulation of cellular response to VEGF","type":"exact"},{"name":"downregulation of cellular response to VEGFA","type":"narrow"},{"name":"downregulation of cellular response to VEGFB","type":"narrow"},{"name":"downregulation of cellular response to vascular endothelial growth factor","type":"exact"},{"name":"downregulation of cellular response to vascular endothelial growth factor stimulus","type":"exact"},{"name":"inhibition of cellular response to VEGF","type":"narrow"},{"name":"inhibition of cellular response to VEGFA","type":"narrow"},{"name":"inhibition of cellular response to VEGFB","type":"narrow"},{"name":"inhibition of cellular response to vascular endothelial growth factor","type":"narrow"},{"name":"inhibition of cellular response to vascular endothelial growth factor stimulus","type":"narrow"},{"name":"negative regulation of cellular response to VEGF","type":"exact"},{"name":"negative regulation of cellular response to VEGFA","type":"narrow"},{"name":"negative regulation of cellular response to VEGFB","type":"narrow"},{"name":"negative regulation of cellular response to vascular endothelial growth factor","type":"exact"}],"termid":"GO:1902548"}


id: MONDO:0007731
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete HLA modifier (obsolete MONDO:0007731)","secondary_identifiers":["OMIM:142770"],"synonyms":[{"name":"HLA modifier","type":"related"}],"termid":"MONDO:0007731","xrefs":{"Monarch":{"xref_id":"0007731"}}}


id: FYPO:0007782
data:
  {"alleles_by_uniquename":{"SJAG_00364:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00364","name":"rad3delta","uniquename":"SJAG_00364:allele-1"},"SJAG_00429:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00429","name":"rad26delta","uniquename":"SJAG_00429:allele-1"},"SJAG_01205:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01205","name":"crb2delta","uniquename":"SJAG_01205:allele-1"},"SJAG_01605:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01605","name":"rad9delta","uniquename":"SJAG_01605:allele-1"},"SJAG_01680:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01680","name":"chk1delta","uniquename":"SJAG_01680:allele-1"},"SJAG_02266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02266","name":"rad24delta","uniquename":"SJAG_02266:allele-1"},"SJAG_02576:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02576","name":"rad25delta","uniquename":"SJAG_02576:allele-1"},"SJAG_02771:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02771","name":"rad1delta","uniquename":"SJAG_02771:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118609,118610,118611,118612,118613,118614,118616,118617,118941,118945],"is_not":false,"summary":null,"term":"FYPO:0007782"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the transition from yeast-form to hyphal growth does not occur under conditions that normally induce it.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal hyphal growth","termid":"FYPO:0007773"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_00429":null,"SJAG_01205":null,"SJAG_01605":null,"SJAG_01680":null,"SJAG_02266":null,"SJAG_02576":null,"SJAG_02771":null},"genotype_count":8,"genotypes_by_uniquename":{"chk1delta":{"display_name":"chk1delta","display_uniquename":"chk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01680:allele-1","expression":"Null"}]}]},"crb2delta":{"display_name":"crb2delta","display_uniquename":"crb2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01205:allele-1","expression":"Null"}]}]},"rad1delta":{"display_name":"rad1delta","display_uniquename":"rad1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02771:allele-1","expression":"Null"}]}]},"rad24delta":{"display_name":"rad24delta","display_uniquename":"rad24delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02266:allele-1","expression":"Null"}]}]},"rad25delta":{"display_name":"rad25delta","display_uniquename":"rad25delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02576:allele-1","expression":"Null"}]}]},"rad26delta":{"display_name":"rad26delta","display_uniquename":"rad26delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00429:allele-1","expression":"Null"}]}]},"rad3delta":{"display_name":"rad3delta","display_uniquename":"rad3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00364:allele-1","expression":"Null"}]}]},"rad9delta":{"display_name":"rad9delta","display_uniquename":"rad9delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01605:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0007773"}],"interesting_parent_ids":["FYPO:0007773","FYPO:0000002"],"is_obsolete":false,"name":"abolished hyphal transition","references_by_uniquename":{"PMID:20368354":null,"PMID:23090706":null},"single_locus_annotated_genes":["SJAG_02576","SJAG_01205","SJAG_01605","SJAG_02771","SJAG_00429","SJAG_02266","SJAG_01680","SJAG_00364"],"single_locus_genotype_uniquenames":["rad1delta","crb2delta","rad26delta","chk1delta","rad3delta","rad24delta","rad9delta","rad25delta"],"synonyms":[{"name":"abolished transition to hyphal growth","type":"exact"},{"name":"hyphal transition abolished","type":"exact"}],"termid":"FYPO:0007782","terms_by_termid":{"FYECO:0000137":null,"FYECO:0000314":null,"FYPO:0007782":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:0098799
data:
  {"annotated_genes":["SJAG_02355","SJAG_00948","SJAG_05259","SJAG_04996","SJAG_03345","SJAG_01305","SJAG_01134","SJAG_03515","SJAG_03358","SJAG_00569","SJAG_03502","SJAG_03415","SJAG_03710","SJAG_01780","SJAG_01951","SJAG_02361","SJAG_04370","SJAG_03416","SJAG_01929"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104288,88762,115211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036266"},{"annotations":[106984,90410,107111,105314,116056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032865"},{"annotations":[111241,109859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140595"},{"annotations":[90405,107031,98924,99037,107052,105643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005742"},{"annotations":[109851,89882,90412,98087],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001401"}]},"cv_name":"cellular_component","definition":"Any protein complex that is part of the outer mitochondrial membrane.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"mitochondrial protein-containing complex","termid":"GO:0098798"},{"relation_name":"part_of","term_name":"mitochondrial outer membrane","termid":"GO:0005741"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00569":null,"SJAG_00948":null,"SJAG_01134":null,"SJAG_01305":null,"SJAG_01780":null,"SJAG_01929":null,"SJAG_01951":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_03345":null,"SJAG_03358":null,"SJAG_03415":null,"SJAG_03416":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03710":null,"SJAG_04370":null,"SJAG_04996":null,"SJAG_05259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005739"}],"interesting_parent_ids":["GO:0005575","GO:0005739","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"outer mitochondrial membrane protein complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0098799","terms_by_termid":{"GO:0001401":null,"GO:0005742":null,"GO:0032865":null,"GO:0036266":null,"GO:0140595":null}}


id: PBO:0000881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L37 (predicted)","termid":"PBO:0000881"}


id: PBO:0038651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acid phosphatase 1","termid":"PBO:0038651"}


id: GO:0097364
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a calcium ion by a channel that opens in response to a mechanical stress in the form of stretching, and contributing to the regulation of action potential.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","PMID:21290758","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stretch-activated, monoatomic cation-selective, calcium channel activity","termid":"GO:0015275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"stretch-activated, monoatomic cation-selective, calcium channel activity involved in regulation of action potential","synonyms":[{"name":"stretch-activated, cation-selective, calcium channel activity involved in regulation of action potential","type":"broad"}],"termid":"GO:0097364"}


id: PBO:0073049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small cysteine and glycine repeat containing 7","termid":"PBO:0073049"}


id: PBO:0054111
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 1476","termid":"PBO:0054111"}


id: MONDO:0015752
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by severe intellectual deficit, kyphosis with onset in childhood and cataract with onset in late adolescence.","definition_xrefs":["Orphanet:171860"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability-cataracts-kyphosis syndrome","termid":"MONDO:0015752","xrefs":{"Monarch":{"xref_id":"0015752"}}}


id: PBO:0041160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic transcription factor 3 pseudogene 15","termid":"PBO:0041160"}


id: PBO:0052247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel tetramerization domain containing 16","termid":"PBO:0052247"}


id: PBO:0108928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FBL pseudogene 1","termid":"PBO:0108928"}


id: PBO:0072157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 34","termid":"PBO:0072157"}


id: PBO:0080737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WW domain containing E3 ubiquitin protein ligase 1 pseudogene 1","termid":"PBO:0080737"}


id: MONDO:0009983
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism is an extremely rare syndromic retinitis pigmentosa characterized by pigmentary retinopathy, diabetes mellitus with hyperinsulinism, acanthosis nigricans, secondary cataracts, neurogenic deafness, short stature mild hypogonadism in males and polycystic ovaries with oligomenorrhea in females. Inheritance is thought to be autosomal recessive. It can be distinguished from Alstrom syndrome by the presence of intellectual disability and the absence of renal insufficiency. There have been no further descriptions in the literature since 1993.","definition_xrefs":["Orphanet:3085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome","secondary_identifiers":["MEDGEN:340317","UMLS:C1849401","OMIM:268020","GARD:4683","MESH:C564841"],"synonyms":[{"name":"insulin-resistant diabetes with acanthosis nigricans, hypogonadism, pigmentary retinopathy, deafness, and intellectual disability","type":"related"},{"name":"insulin-resistant diabetes with acanthosis nigricans, hypogonadism, pigmentary retinopathy, deafness, and mental retardation","type":"related"},{"name":"retinitis pigmentosa, deafness, intellectual disability, and hypogonadism","type":"related"},{"name":"retinitis pigmentosa, deafness, mental retardation, and hypogonadism","type":"related"},{"name":"retinitis pigmentosa-intellectual disability- labyrinthine deafness-hypogenitalism syndrome","type":"exact"},{"name":"retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome","type":"related"},{"name":"retinitis pigmentosa-intellectual disability-sensorineural hearing loss-hypogenitalism syndrome","type":"exact"}],"termid":"MONDO:0009983","xrefs":{"Monarch":{"xref_id":"0009983"}}}


id: PBO:0108605
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_characteristic","termid":"PBO:0108605"}


id: MONDO:0007606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in characteristic extraskeletal sites.","definition_xrefs":["Orphanet:337"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments (obsolete MONDO:0018231)","termid":"MONDO:0018231"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"subcutaneous tissue disorder","termid":"MONDO:0019296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrodysplasia ossificans progressiva","secondary_identifiers":["MEDGEN:4698","NANDO:1200871","NANDO:2201020","NORD:1143","SCTID:82725007","UMLS:C0016037","icd11.foundation:2102976705","NCIT:C3040","OMIM:135100","DOID:13374","GARD:6445","ICD9:728.11","MESH:D009221","MedDRA:10068715"],"synonyms":[{"name":"FOP","type":"exact"},{"name":"Stone Man syndrome","type":"exact"},{"name":"Stone man syndrome","type":"exact"},{"name":"fibrodysplasia ossificans progressiva","type":"exact"},{"name":"fop","type":"exact"},{"name":"myositis ossificans progressiva","type":"related"},{"name":"progressive myositis ossificans","type":"exact"},{"name":"progressive ossifying myositis","type":"exact"}],"termid":"MONDO:0007606","xrefs":{"Monarch":{"xref_id":"0007606"}}}


id: GO:1905413
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of dense core granule exocytosis.","definition_xrefs":["GOC:PARL","GOC:TermGenie","GO_REF:0000058","PMID:18468511","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of calcium ion-dependent exocytosis","termid":"GO:0017158"},{"relation_name":"regulates","term_name":"dense core granule exocytosis","termid":"GO:1990504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"regulation of dense core granule exocytosis","synonyms":[{"name":"regulation of dense core vesicle exocytosis","type":"exact"}],"termid":"GO:1905413"}


id: MONDO:0010455
data:
  {"annotated_genes":["SJAG_03333"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86415],"is_not":false,"summary":null,"term":"MONDO:0010455"}]},"cv_name":"mondo","definition":"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia is a rare combined T and B cell immunodeficiency characterized by recurrent sinopulmonary and viral infections, persistent elevated Epstein-Barr virus (EBV) viremia and increased susceptibility to EBV-associated B-cell lymphoproliferative disorders. Immunological analyzes show normal lymphocyte count or mild to moderate lymphopenia, inverted CD4:CD8 T-cell ratio and hypogammaglobulinemias.","definition_xrefs":["Orphanet:317476"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"combined immunodeficiency","termid":"MONDO:0015131"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03333":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:10907","SCTID:711481001","MEDGEN:477076","OMIM:300853","DOID:0080319","NCIT:C126336","UMLS:C3275445"],"synonyms":[{"name":"Cid due to MAGT1 deficiency","type":"exact"},{"name":"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia","type":"exact"},{"name":"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia","type":"related"},{"name":"X-linked magnesium deficiency with Epstein-Barr virus infection and neoplasia","type":"related"},{"name":"XMEN","type":"exact"},{"name":"combined immunodeficiency due to MAGT1 deficiency","type":"exact"},{"name":"immunodeficiency, X-linked, with magnesium defect, Epstein-Barr VIRUS infection, and neoplasia","type":"related"},{"name":"immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia, X-linked recessive","type":"exact"}],"termid":"MONDO:0010455","terms_by_termid":{"MONDO:0010455":null},"xrefs":{"Monarch":{"xref_id":"0010455"}}}


id: SO:0001751
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A SL2_acceptor_site which appends the SL6 RNA leader sequence to the 5' end of an mRNA. SL6 acceptor sites occur in genes in internal segments of polycistronic transcripts.","definition_xrefs":["SO:nlw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SL2_acceptor_site","termid":"SO:0000709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SL6_acceptor_site","synonyms":[{"name":"SL6 acceptor site","type":"exact"}],"termid":"SO:0001751"}


