# terms

id: GO:0009991
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an extracellular stimulus.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete response to extracellular stimulus (obsolete GO:0009991)","termid":"GO:0009991"}


id: FYPO:0006801
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 spindle pole bodies (SPBs) than normal. In this phenotype, extra SPBs typically contain normal components but seldom attach to spindle microtubules.","definition_xrefs":["PMID:9763447","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"output_of","term_name":"abnormal mitotic spindle pole body duplication","termid":"FYPO:0001791"}],"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:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"spindle pole bodies present in increased numbers during vegetative growth","synonyms":[{"name":"SPBs present in increased numbers during vegetative growth","type":"exact"},{"name":"excess mitotic spindle pole bodies present","type":"exact"},{"name":"excess spindle pole bodies present during vegetative growth","type":"exact"},{"name":"extra spindle pole bodies present during vegetative growth","type":"exact"},{"name":"multiple mitotic spindle pole bodies","type":"exact"},{"name":"overreplicated mitotic spindle pole bodies","type":"related"},{"name":"spindle pole bodies present in greater numbers during vegetative growth","type":"exact"},{"name":"spindle pole bodies present in increased numbers during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006801"}


id: MONDO:0012242
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":"syncope, familial vasovagal","secondary_identifiers":["MEDGEN:373086","OMIM:609289","UMLS:C1836438","MESH:C536849"],"synonyms":[{"name":"VVS","type":"exact"},{"name":"familial neurocardiogenic syncope","type":"related"},{"name":"familial vasovagal syncope","type":"related"},{"name":"syncope familial neurocardiogenic","type":"related"},{"name":"syncope, familial Neurocardiogenic","type":"related"},{"name":"syncope, familial VASOVAGAL","type":"related"}],"termid":"MONDO:0012242","xrefs":{"Monarch":{"xref_id":"0012242"}}}


id: PR:Q10200
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC11C11.01 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10200"],"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 C11C11.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC11C11.01","synonyms":[{"name":"Spom972h-SPBC11C11.01","type":"exact"}],"termid":"PR:Q10200"}


id: MONDO:0003283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the epididymis. Representative examples include epididymal adenomatoid tumor and epididymal adenocarcinoma.","definition_xrefs":["NCIT:C39958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system neoplasm","termid":"MONDO:0024582"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epididymal neoplasm","secondary_identifiers":["UMLS:C0346239","DOID:512","ICD9:239.5","MEDGEN:138047","SCTID:126902008"],"synonyms":[{"name":"epididymal neoplasm","type":"exact"},{"name":"epididymis neoplasm","type":"exact"},{"name":"epididymis neoplasm (disease)","type":"exact"},{"name":"epididymis tumor","type":"exact"},{"name":"epididymis tumour","type":"exact"},{"name":"neoplasm of epididymis","type":"exact"},{"name":"neoplasm of epididymus","type":"exact"},{"name":"tumor of epididymis","type":"exact"},{"name":"tumour of epididymis","type":"exact"}],"termid":"MONDO:0003283","xrefs":{"Monarch":{"xref_id":"0003283"}}}


id: PBO:0113093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic seryl-tRNA synthetase; class II aminoacyl-tRNA synthetase that aminoacylates tRNA(Ser), displays tRNA-dependent amino acid recognition which enhances discrimination of the serine substrate; copurifies with Abp140p in an RNA-dependent manner and stimulates 3-methylcytidine (m3C) modification of residue 32 of the tRNA anticodon loop of tRNA-Ser; interacts with peroxin Pex21p","termid":"PBO:0113093"}


id: PBO:0017882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine diphosphate-N-acetylglucosamine transmembrane transporter Hut1","termid":"PBO:0017882"}


id: MONDO:0017685
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin B12-responsive methylmalonic acidemia","termid":"MONDO:0017214"},{"relation_name":"is_a","term_name":"methylmalonic aciduria and/or homocystinuria, cblD type","termid":"MONDO:0100463"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"vitamin B12-responsive methylmalonic acidemia, type cblDv2","secondary_identifiers":["MEDGEN:376388","Orphanet:308442","GARD:17391","UMLS:C1848554"],"synonyms":[{"name":"vitamin B12-responsive methylmalonic aciduria, type cblDv2","type":"exact"}],"termid":"MONDO:0017685","xrefs":{"Monarch":{"xref_id":"0017685"}}}


id: PATO:0002316
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Being separate or discrete from other skeletal elements.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autogenous","synonyms":[{"name":"free","type":"related"}],"termid":"PATO:0002316"}


id: PBO:0075008
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 115-19","termid":"PBO:0075008"}


id: GO:2000660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of interleukin-1-mediated signaling pathway.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine-mediated signaling pathway","termid":"GO:0001960"},{"relation_name":"is_a","term_name":"regulation of interleukin-1-mediated signaling pathway","termid":"GO:2000659"},{"relation_name":"negatively_regulates","term_name":"interleukin-1-mediated signaling pathway","termid":"GO:0070498"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of interleukin-1-mediated signaling pathway","synonyms":[{"name":"negative regulation of IL-1 alpha-mediated signaling pathway","type":"related"},{"name":"negative regulation of IL-1 beta-mediated signaling pathway","type":"related"},{"name":"negative regulation of IL-1-mediated signaling pathway","type":"exact"},{"name":"negative regulation of interleukin-1 alpha-mediated signaling pathway","type":"related"},{"name":"negative regulation of interleukin-1 beta-mediated signaling pathway","type":"related"},{"name":"negative regulation of interleukin-1-mediated signalling pathway","type":"exact"}],"termid":"GO:2000660"}


id: PBO:0049627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 30","termid":"PBO:0049627"}


id: PBO:0001467
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monomeric","termid":"PBO:0001467"}


id: MONDO:0013561
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with multiple joint dislocations (obsolete MONDO:0019700)","termid":"MONDO:0019700"},{"relation_name":"is_a","term_name":"mineral metabolism disease","termid":"MONDO:0000226"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"chondrodysplasia with joint dislocations, gPAPP type","secondary_identifiers":["DOID:0112224","GARD:11009","OMIM:614078","UMLS:C3279757","MEDGEN:481387","Orphanet:280586"],"synonyms":[{"name":"chondrodysplasia with joint dislocations, gPAPP type","type":"exact"},{"name":"gPAPP deficiency","type":"exact"}],"termid":"MONDO:0013561","xrefs":{"Monarch":{"xref_id":"0013561"}}}


id: MONDO:0001171
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of salpingo-oophoritis.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salpingo-oophoritis","termid":"MONDO:0001172"},{"relation_name":"is_a","term_name":"acute salpingitis","termid":"MONDO:0001173"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute salpingo-oophoritis","secondary_identifiers":["DOID:10971","SCTID:266581008","UMLS:C0156327","ICD9:614.0","MEDGEN:510243"],"synonyms":[{"name":"acute salpingitis and oophoritis","type":"exact"},{"name":"salpingo-oophoritis, acute","type":"exact"}],"termid":"MONDO:0001171","xrefs":{"Monarch":{"xref_id":"0001171"}}}


id: GO:0098687
data:
  {"annotated_genes":["SJAG_03982","SJAG_01745","SJAG_00082","SJAG_00666","SJAG_03832","SJAG_01675","SJAG_00676","SJAG_04581","SJAG_02807","SJAG_04038","SJAG_04186","SJAG_04140","SJAG_04863","SJAG_05260","SJAG_03491","SJAG_00806","SJAG_04745","SJAG_03287","SJAG_01228","SJAG_01605","SJAG_02768","SJAG_03437","SJAG_04586","SJAG_03161","SJAG_02990","SJAG_04097","SJAG_01378","SJAG_03567","SJAG_00229","SJAG_02194","SJAG_05319","SJAG_04205","SJAG_03720","SJAG_03350","SJAG_02116","SJAG_01613","SJAG_00350","SJAG_01836","SJAG_03042","SJAG_03418","SJAG_03092","SJAG_04253","SJAG_02336","SJAG_03664","SJAG_02212","SJAG_05979","SJAG_03789","SJAG_00640","SJAG_03685","SJAG_05353","SJAG_04039","SJAG_00935","SJAG_01332","SJAG_01698","SJAG_04126","SJAG_05173","SJAG_02818","SJAG_02872","SJAG_00207","SJAG_01330","SJAG_02927","SJAG_01864","SJAG_02773","SJAG_00483","SJAG_00768","SJAG_01224","SJAG_02465","SJAG_03867","SJAG_01837","SJAG_02119","SJAG_04508","SJAG_04201","SJAG_04700","SJAG_04150","SJAG_00378","SJAG_00170","SJAG_04142","SJAG_02348","SJAG_04696","SJAG_00414","SJAG_01046","SJAG_00302","SJAG_04141","SJAG_06560","SJAG_02771","SJAG_04183","SJAG_04699","SJAG_03681","SJAG_00335","SJAG_01377","SJAG_03945","SJAG_03989","SJAG_04372","SJAG_04245","SJAG_00697","SJAG_02362","SJAG_02814","SJAG_04259","SJAG_02863","SJAG_00293","SJAG_03916","SJAG_02761","SJAG_02621","SJAG_01410","SJAG_00429","SJAG_05239","SJAG_00918","SJAG_04040","SJAG_02451","SJAG_01082","SJAG_04076","SJAG_01546","SJAG_02563","SJAG_02731","SJAG_02401","SJAG_02846","SJAG_03635","SJAG_03220","SJAG_03780","SJAG_00418","SJAG_00939","SJAG_04884","SJAG_04841","SJAG_03356","SJAG_00884","SJAG_00794","SJAG_02908","SJAG_03855","SJAG_05220","SJAG_04177","SJAG_01371","SJAG_01067","SJAG_03126","SJAG_02664","SJAG_01928","SJAG_01777","SJAG_03942","SJAG_03680","SJAG_03722","SJAG_04574","SJAG_01050","SJAG_01717","SJAG_01831","SJAG_03540","SJAG_03543","SJAG_02866","SJAG_00678","SJAG_02513","SJAG_04190","SJAG_03926","SJAG_00684","SJAG_00307","SJAG_00934","SJAG_00364","SJAG_05266","SJAG_04412","SJAG_05105","SJAG_02576","SJAG_03683","SJAG_03619","SJAG_03327","SJAG_01211","SJAG_05372","SJAG_05373","SJAG_05321","SJAG_06642","SJAG_03217","SJAG_02346","SJAG_01775","SJAG_01873","SJAG_01297","SJAG_03128","SJAG_02624","SJAG_03298","SJAG_00756","SJAG_03997","SJAG_04670","SJAG_05329","SJAG_03449","SJAG_01540","SJAG_03183","SJAG_01075","SJAG_03026","SJAG_01601","SJAG_01579","SJAG_00600","SJAG_03844","SJAG_06597","SJAG_04255","SJAG_02778","SJAG_04623","SJAG_05273","SJAG_04030","SJAG_05019","SJAG_03460","SJAG_03689","SJAG_01805","SJAG_01278","SJAG_04400","SJAG_00646","SJAG_02409","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[115963,91573,101547,105766,109120,116590,89572,111396,90838],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061638"},{"annotations":[101548],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043505"},{"annotations":[90288,107608,111624,116883],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061838"},{"annotations":[113932,116591,117602,88582,115912,105656,89193,101550,87510,90839,109762,111128,112818],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0034506"},{"annotations":[116101,108595,112661,95810,100756,104939,105731,106286,89194,101551,98551,88865,109122,111625,113933,115336,101919,87511,103976,110663,94803,114520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000775"},{"annotations":[88583,89553,107615,90840,88866,110664,117141,117986,87377,99051,103662,116299,105767,113718,91291,113854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099115"},{"annotations":[118806,118703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000781"},{"annotations":[91340,92220,100346,58655,92027,88628,106076,100624,92221,61032,90934,94586,103663,97785,106807,108562,91574,111544,109821,90141,92222,98956,110635,92219,107578,59956,86915,65638,115674,115691,101832,112726,96923,112370,112373,58401,107391,111171,113719,104567,114961,59635,66120,112266,108835,116102,115381,110978,117519,89269,98684,99227,107616,99411,115760,110392,103628,59738,114051,59120,118049,111951,112369,68875,63512,112319,110992,68990,112372,65790,99217,105608,109670,88052,112371,99052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140445"},{"annotations":[98116,95058,87320,89250,98614,107280,116300,115363,111626,101552,101920,109763,94804,109808,89574,107200,105011,90485,94197,108596,113216,100003,107244,113573,104940,89195,98762,112662,106960,93804,90427,112555,90773],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000779"},{"annotations":[109822,114052],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990879"},{"annotations":[88652,90487,116357,89252,98118,106962,113537,108340,100005,109350],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0042729"},{"annotations":[116103,105013,89546,113934,115339,113574,112663,109764,111627,98764,89196],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000939"},{"annotations":[105828,90488,109809,99623,100006,98765,104941,89197,101835,109765,94265,106963,112556,87513,99861,115364,113935,109362,113575,114996,98119,116104,103368,114005,118121,90289,108668,113217,107704,117570,108598,112664,105780,94805,112990,118085,93286,88868,89547,98708,101921,101283,96777,100819,118284,111628,111494,89493,95059,118733,112822,114522,111338,94199,97401,93702,96262,118685],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000776"},{"annotations":[100820,113218],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0180019"},{"annotations":[109810,98766,109766,95060],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000444"},{"annotations":[105829,89548,94200,105014,113576,89198,93806,112991,114006,112557,97402],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031511"},{"annotations":[111131,87515],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033551"},{"annotations":[108599,101922,115365,94807],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031262"},{"annotations":[104569],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000783"},{"annotations":[89256,99868,95061,109768,115367,98124,101924,113939,118092,113219],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000940"},{"annotations":[95659,112499,116305,117523,107619,91885,112046,111550,102705,112730,90432,117990,106008,106793,117134,113425,93580,90777,103667,118126,90917,105769,99106,91295,98619,109934,115425,107284,116564,98462,117145,103571,112048,101491,101325,88872,110660,101490,87381,112668,102263,113859,87158,113723,111651,117191,91576,93596,113110,114011,112047,93329,96228,101489,118246,99058,89557,90848],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005721"},{"annotations":[89274,115384,91343,94589,99218,104572],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070187"},{"annotations":[117135,111653,101492,101494,109935,111553,99059,103572,90779,93581,102706,117192,91579,90433,112049,93330,115385,113427,101493,96229,112051,117525,103670,112733,112050,118248,95660,116565,98620],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140720"},{"annotations":[114053,99219,107396,109824,115386,94590],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000782"}]},"cv_name":"cellular_component","definition":"Any subdivision of a chromosome along its length.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"chromosome","termid":"GO:0005694"}],"gene_count":202,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00170":null,"SJAG_00207":null,"SJAG_00229":null,"SJAG_00293":null,"SJAG_00302":null,"SJAG_00307":null,"SJAG_00335":null,"SJAG_00350":null,"SJAG_00364":null,"SJAG_00378":null,"SJAG_00414":null,"SJAG_00418":null,"SJAG_00429":null,"SJAG_00483":null,"SJAG_00600":null,"SJAG_00640":null,"SJAG_00646":null,"SJAG_00666":null,"SJAG_00676":null,"SJAG_00678":null,"SJAG_00684":null,"SJAG_00697":null,"SJAG_00756":null,"SJAG_00768":null,"SJAG_00794":null,"SJAG_00806":null,"SJAG_00884":null,"SJAG_00918":null,"SJAG_00934":null,"SJAG_00935":null,"SJAG_00939":null,"SJAG_01046":null,"SJAG_01050":null,"SJAG_01067":null,"SJAG_01075":null,"SJAG_01082":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01228":null,"SJAG_01278":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01332":null,"SJAG_01371":null,"SJAG_01377":null,"SJAG_01378":null,"SJAG_01410":null,"SJAG_01540":null,"SJAG_01546":null,"SJAG_01579":null,"SJAG_01601":null,"SJAG_01605":null,"SJAG_01613":null,"SJAG_01675":null,"SJAG_01698":null,"SJAG_01717":null,"SJAG_01745":null,"SJAG_01775":null,"SJAG_01777":null,"SJAG_01805":null,"SJAG_01831":null,"SJAG_01836":null,"SJAG_01837":null,"SJAG_01864":null,"SJAG_01873":null,"SJAG_01928":null,"SJAG_02116":null,"SJAG_02119":null,"SJAG_02194":null,"SJAG_02212":null,"SJAG_02336":null,"SJAG_02346":null,"SJAG_02348":null,"SJAG_02362":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02451":null,"SJAG_02465":null,"SJAG_02513":null,"SJAG_02563":null,"SJAG_02576":null,"SJAG_02621":null,"SJAG_02624":null,"SJAG_02664":null,"SJAG_02731":null,"SJAG_02761":null,"SJAG_02768":null,"SJAG_02771":null,"SJAG_02773":null,"SJAG_02778":null,"SJAG_02807":null,"SJAG_02814":null,"SJAG_02818":null,"SJAG_02846":null,"SJAG_02863":null,"SJAG_02866":null,"SJAG_02872":null,"SJAG_02908":null,"SJAG_02927":null,"SJAG_02990":null,"SJAG_03026":null,"SJAG_03042":null,"SJAG_03048":null,"SJAG_03092":null,"SJAG_03126":null,"SJAG_03128":null,"SJAG_03161":null,"SJAG_03183":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03287":null,"SJAG_03298":null,"SJAG_03327":null,"SJAG_03350":null,"SJAG_03356":null,"SJAG_03418":null,"SJAG_03437":null,"SJAG_03449":null,"SJAG_03460":null,"SJAG_03491":null,"SJAG_03540":null,"SJAG_03543":null,"SJAG_03567":null,"SJAG_03619":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03683":null,"SJAG_03685":null,"SJAG_03689":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03780":null,"SJAG_03789":null,"SJAG_03832":null,"SJAG_03844":null,"SJAG_03855":null,"SJAG_03867":null,"SJAG_03916":null,"SJAG_03926":null,"SJAG_03942":null,"SJAG_03945":null,"SJAG_03982":null,"SJAG_03989":null,"SJAG_03997":null,"SJAG_04030":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04040":null,"SJAG_04076":null,"SJAG_04097":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04141":null,"SJAG_04142":null,"SJAG_04150":null,"SJAG_04177":null,"SJAG_04183":null,"SJAG_04186":null,"SJAG_04190":null,"SJAG_04201":null,"SJAG_04205":null,"SJAG_04245":null,"SJAG_04253":null,"SJAG_04255":null,"SJAG_04259":null,"SJAG_04372":null,"SJAG_04400":null,"SJAG_04412":null,"SJAG_04508":null,"SJAG_04574":null,"SJAG_04581":null,"SJAG_04586":null,"SJAG_04623":null,"SJAG_04670":null,"SJAG_04696":null,"SJAG_04699":null,"SJAG_04700":null,"SJAG_04745":null,"SJAG_04841":null,"SJAG_04863":null,"SJAG_04884":null,"SJAG_05019":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05220":null,"SJAG_05239":null,"SJAG_05260":null,"SJAG_05266":null,"SJAG_05273":null,"SJAG_05319":null,"SJAG_05321":null,"SJAG_05329":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_05979":null,"SJAG_06560":null,"SJAG_06597":null,"SJAG_06642":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005575","GO:0005694"],"is_obsolete":false,"name":"chromosomal region","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null,"PMID:21802294":null,"PMID:24184107":null,"PMID:32109380":null},"synonyms":[{"name":"chromosome region","type":"exact"}],"termid":"GO:0098687","terms_by_termid":{"GO:0000444":null,"GO:0000775":null,"GO:0000776":null,"GO:0000779":null,"GO:0000781":null,"GO:0000782":null,"GO:0000783":null,"GO:0000939":null,"GO:0000940":null,"GO:0005721":null,"GO:0031262":null,"GO:0031511":null,"GO:0033551":null,"GO:0034506":null,"GO:0042729":null,"GO:0043505":null,"GO:0061638":null,"GO:0061838":null,"GO:0070187":null,"GO:0099115":null,"GO:0140445":null,"GO:0140720":null,"GO:0180019":null,"GO:1990879":null}}


id: FYPO:0002993
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during a cellular response to methyl methanesulfonate.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during vegetative growth","termid":"FYPO:0001838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0002494","FYPO:0002274","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein phosphorylation during cellular response to methyl methanesulfonate","synonyms":[{"name":"decreased protein phosphorylation during cellular response to MMS","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to methyl methanesulfonate during mitotic cell cycle","type":"related"},{"name":"decreased protein phosphorylation during cellular response to methyl methanesulfonate during vegetative growth","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to methyl methanesulphonate","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to MMS","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to methyl methanesulfonate","type":"exact"}],"termid":"FYPO:0002993"}


id: PBO:0091214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pdc2-Repressed lncRNA, SPAC212.12 antisense","termid":"PBO:0091214"}


id: PBO:0001158
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zellweger syndrome","termid":"PBO:0001158"}


id: MONDO:0016572
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Central bilateral macrogyria is a neuronal migration disorder characterized by pseudobulbar palsy, developmental delay, mild mental retardation and epilepsy. It has been described in at least four children.","definition_xrefs":["Orphanet:2431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral cortical dysplasia","termid":"MONDO:0017094"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"central bilateral macrogyria","secondary_identifiers":["icd11.foundation:67804763","SCTID:720632004","MEDGEN:929618","UMLS:C4303949"],"termid":"MONDO:0016572","xrefs":{"Monarch":{"xref_id":"0016572"}}}


id: GO:0086038
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: Ca2+(in) + Na+(out) = Ca2+(out) + Na+(in), which contributes to regulating the membrane potential of a cardiac muscle cell.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium:sodium antiporter activity","termid":"GO:0005432"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"calcium:sodium antiporter activity involved in regulation of cardiac muscle cell membrane potential","termid":"GO:0086038"}


id: PBO:0085516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the small (40S) ribosomal subunit; homologous to mammalian ribosomal protein S16 and bacterial S9; RPS16B has a paralog, RPS16A, that arose from the whole genome duplication","termid":"PBO:0085516"}


id: GO:0035001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Growth of epithelial tubes that originate from pits in an open tracheal system and grow towards each other to meet and form a continuous open tube called the dorsal trunk. The dorsal trunk extends from the anterior spiracle to the posterior spiracle of the larva and forms the main airway of the insect tracheal system.","definition_xrefs":["ISBN:0879694238","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental growth involved in morphogenesis","termid":"GO:0060560"},{"relation_name":"part_of","term_name":"open tracheal system development","termid":"GO:0007424"}],"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":"dorsal trunk growth, open tracheal system","synonyms":[{"name":"dorsal trunk growth","type":"related"}],"termid":"GO:0035001"}


id: GO:0035261
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the external genitalia are generated and organized. The external genitalia are the outer sex organs, such as the penis or vulva in mammals.","definition_xrefs":["PMID:25247640","PMID:24793987"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genitalia morphogenesis","termid":"GO:0035112"}],"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":"external genitalia morphogenesis","termid":"GO:0035261"}


id: GO:0021878
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into an astrocyte that resides in the forebrain.","definition_xrefs":["GOC:cls","GOC:jid","PMID:16226447","GOC:dgh","GO_REF:0000021","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"astrocyte fate commitment","termid":"GO:0060018"},{"relation_name":"part_of","term_name":"forebrain astrocyte differentiation","termid":"GO:0021896"}],"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 astrocyte fate commitment","termid":"GO:0021878"}


id: GO:0050559
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: all-trans-geranylgeranyl diphosphate = (+)-copalyl diphosphate.","definition_xrefs":["EC:5.5.1.12","RHEA:24316"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular lyase activity","termid":"GO:0016872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"copalyl diphosphate synthase activity","secondary_identifiers":["MetaCyc:RXN-4861","KEGG_REACTION:R06298"],"synonyms":[{"name":"(+)-copalyl-diphosphate lyase (decyclizing)","type":"related"},{"name":"diterpene cyclase activity","type":"broad"}],"termid":"GO:0050559"}


id: FYPO:0002198
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which all cells in the population are viable but have abnormal cell shape, in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete viable vegetative cell population with abnormal cell shape (obsolete FYPO:0002198)","synonyms":[{"name":"viable, abnormally shaped vegetative cell population","type":"exact"}],"termid":"FYPO:0002198"}


id: PBO:0074971
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 114-13","termid":"PBO:0074971"}


id: GO:0015187
data:
  {"annotated_genes":["SJAG_04984","SJAG_00626"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97731,99733],"is_not":false,"summary":null,"term":"GO:0015187"}]},"cv_name":"molecular_function","definition":"Enables the transfer of glycine from one side of a membrane to the other. Glycine is aminoethanoic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"},{"relation_name":"is_a","term_name":"L-amino acid transmembrane transporter activity","termid":"GO:0015179"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00626":null,"SJAG_04984":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"glycine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"glycine betaine/proline porter activity","type":"narrow"},{"name":"glycine transporter activity","type":"broad"},{"name":"proline/glycine/betaine:hydrogen/sodium symporter activity","type":"narrow"}],"termid":"GO:0015187","terms_by_termid":{"GO:0015187":null}}


id: PBO:0048638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gap junction protein alpha 8","termid":"PBO:0048638"}


id: MONDO:0001654
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the spermatic cord.","direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive organ cancer","termid":"MONDO:0005836"}],"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":"spermatic cord cancer","secondary_identifiers":["NCIT:C3559","DOID:13169","MEDGEN:102278","UMLS:C0153603","SCTID:363453008","ICD9:187.6"],"synonyms":[{"name":"cancer of spermatic cord","type":"exact"},{"name":"malignant neoplasm of spermatic cord","type":"exact"},{"name":"malignant neoplasm of the spermatic cord","type":"exact"},{"name":"malignant spermatic cord neoplasm","type":"exact"},{"name":"malignant spermatic cord tumor","type":"exact"},{"name":"malignant spermatic cord tumour","type":"exact"},{"name":"malignant tumor of spermatic cord","type":"exact"},{"name":"malignant tumor of the spermatic cord","type":"exact"},{"name":"malignant tumour of spermatic cord","type":"exact"},{"name":"malignant tumour of the spermatic cord","type":"exact"},{"name":"spermatic cord Ca","type":"exact"},{"name":"spermatic cord cancer","type":"exact"}],"termid":"MONDO:0001654","xrefs":{"Monarch":{"xref_id":"0001654"}}}


id: GO:0050270
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-homocysteine + H2O + H+ = S-inosyl-L-homocysteine + NH4.","definition_xrefs":["EC:3.5.4.28","RHEA:20716"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines","termid":"GO:0016814"},{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016810","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"S-adenosylhomocysteine deaminase activity","secondary_identifiers":["KEGG_REACTION:R00193","MetaCyc:S-ADENOSYLHOMOCYSTEINE-DEAMINASE-RXN"],"synonyms":[{"name":"S-adenosyl-L-homocysteine aminohydrolase activity","type":"related"},{"name":"adenosylhomocysteine deaminase activity","type":"related"}],"termid":"GO:0050270"}


id: PR:Q12238
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- uvi31 gene.","definition_xrefs":["UniProtKB:Q12238","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":"UV-induced protein uvi31 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16E9.06c","synonyms":[{"name":"Spom972h-uvi31","type":"exact"}],"termid":"PR:Q12238"}


id: MONDO:0021148
data:
  {"annotated_genes":["SJAG_02748","SJAG_01419","SJAG_01156"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86790,84573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011962"},{"annotations":[86651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032747"}]},"cv_name":"mondo","definition":"A benign, precancerous, or malignant neoplasm that affects the female reproductive system. Representative examples include uterine corpus leiomyoma, endocervical polyp, ovarian carcinoma, cervical carcinoma, and endometrial carcinoma.","definition_xrefs":["NCIT:C3053"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"},{"relation_name":"is_a","term_name":"reproductive system neoplasm","termid":"MONDO:0006054"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01156":null,"SJAG_01419":null,"SJAG_02748":null},"genotype_count":0,"is_obsolete":false,"name":"female reproductive system neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:9004","MESH:D005833","UMLS:C0017416"],"synonyms":[{"name":"female reproductive organ neoplasm (disease)","type":"exact"},{"name":"female reproductive organ tumor","type":"exact"},{"name":"female reproductive organ tumour","type":"exact"},{"name":"female reproductive system neoplasm","type":"exact"},{"name":"female reproductive system neoplasm (disease)","type":"exact"},{"name":"female reproductive system tumor","type":"exact"},{"name":"female reproductive system tumour","type":"exact"},{"name":"gynecologic neoplasm","type":"exact"},{"name":"gynecologic tumor","type":"exact"},{"name":"gynecologic tumour","type":"exact"},{"name":"neoplasm of female reproductive organ","type":"exact"},{"name":"neoplasm of female reproductive system","type":"exact"},{"name":"neoplasm of the female reproductive system","type":"exact"},{"name":"tumor of female reproductive system","type":"exact"},{"name":"tumor of the female reproductive system","type":"exact"},{"name":"tumour of female reproductive system","type":"exact"},{"name":"tumour of the female reproductive system","type":"exact"}],"termid":"MONDO:0021148","terms_by_termid":{"MONDO:0011962":null,"MONDO:0032747":null},"xrefs":{"Monarch":{"xref_id":"0021148"}}}


id: GO:0050440
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + oxaloacetate + propanoyl-CoA = (2R,3S)-2-methylcitrate + CoA + H+.","definition_xrefs":["RHEA:23780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, acyl groups converted into alkyl on transfer","termid":"GO:0046912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016746"],"is_obsolete":false,"name":"2-methylcitrate synthase activity","secondary_identifiers":["MetaCyc:2-METHYLCITRATE-SYNTHASE-RXN","KEGG_REACTION:R00931","EC:2.3.3.5"],"synonyms":[{"name":"2-methylcitrate oxaloacetate-lyase activity","type":"related"},{"name":"MCS activity","type":"related"},{"name":"methylcitrate synthase activity","type":"related"},{"name":"methylcitrate synthetase activity","type":"related"},{"name":"propanoyl-CoA:oxaloacetate C-propanoyltransferase (thioester-hydrolysing, 1-carboxyethyl-forming)","type":"related"}],"termid":"GO:0050440"}


id: PATO:0001922
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being positioned towards the rear of an organism.","definition_xrefs":["PATOC:mb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalised","termid":"PATO:0000628"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mislocalised posteriorly","termid":"PATO:0001922"}


id: MONDO:0005123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Hibiscus chlorotic ringspot virus infection (obsolete MONDO:0005123)","termid":"MONDO:0005123","xrefs":{"Monarch":{"xref_id":"0005123"}}}


id: GO:0003079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of natriuresis.","definition_xrefs":["GOC:mtg_cardio"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of natriuresis (obsolete GO:0003079)","synonyms":[{"name":"positive regulation of natriuresis","type":"exact"}],"termid":"GO:0003079"}


id: GO:0016327
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The apical end of the lateral plasma membrane of epithelial cells.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"apicolateral plasma membrane","synonyms":[{"name":"apical lateral plasma membrane","type":"exact"}],"termid":"GO:0016327"}


id: PBO:0058325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4698","termid":"PBO:0058325"}


id: MONDO:0005436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Postoperative ventricular dysfunction (VnD) occurs in 9-20% of coronary artery bypass graft (CABG) surgical patients and is associated with increased postoperative morbidity and mortality.","definition_xrefs":["EFO:0004889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coronary artery disorder","termid":"MONDO:0005010"},{"relation_name":"is_a","term_name":"cardiac ventricle disorder","termid":"MONDO:0045001"}],"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":"postoperative ventricular dysfunction","termid":"MONDO:0005436","xrefs":{"Monarch":{"xref_id":"0005436"}}}


id: MONDO:0030993
data:
  {"annotated_genes":["SJAG_00336","SJAG_00303","SJAG_03542"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86351,86352,86353],"is_not":false,"summary":null,"term":"MONDO:0030993"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Tessadori-Van-Haaften neurodevelopmental syndrome","termid":"MONDO:0031400"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00303":null,"SJAG_00336":null,"SJAG_03542":null},"genotype_count":0,"is_obsolete":false,"name":"Tessadori-Van Haaften neurodevelopmental syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1824083","UMLS:C5774310","OMIM:619950"],"synonyms":[{"name":"TEVANED3","type":"exact"},{"name":"Tessadori-Van Haaften neurodevelopmental syndrome 3","type":"exact"}],"termid":"MONDO:0030993","terms_by_termid":{"MONDO:0030993":null},"xrefs":{"Monarch":{"xref_id":"0030993"}}}


id: MONDO:0013188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dysequilibrium syndrome in which the cause of the disease is a mutation in the CA8 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar ataxia, intellectual disability, and dysequilibrium","termid":"MONDO:0009133"}],"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":"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3","secondary_identifiers":["MEDGEN:442496","MESH:C567690","OMIM:613227","UMLS:C2750509","DOID:0070558","GARD:15634"],"synonyms":[{"name":"CA8 dysequilibrium syndrome","type":"exact"},{"name":"CAMRQ3","type":"related"},{"name":"cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 3","type":"related"},{"name":"cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3","type":"related"},{"name":"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3","type":"exact"},{"name":"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 3","type":"exact"},{"name":"cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3","type":"exact"},{"name":"cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 3","type":"exact"},{"name":"dysequilibrium syndrome caused by mutation in CA8","type":"exact"}],"termid":"MONDO:0013188","xrefs":{"Monarch":{"xref_id":"0013188"}}}


id: GO:0035278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An RNA interference pathway in which microRNAs (miRNAs) block the translation of target mRNAs into proteins. Once incorporated into a RNA-induced silencing complex (RISC), a miRNA will typically mediate repression of translation if the miRNA imperfectly base-pairs with the 3' untranslated regions of target mRNAs.","definition_xrefs":["PMID:15196554","PMID:14744438"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of translation","termid":"GO:0017148"},{"relation_name":"is_a","term_name":"miRNA-mediated post-transcriptional gene silencing","termid":"GO:0035195"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"miRNA-mediated gene silencing by inhibition of translation","synonyms":[{"name":"down regulation of translation involved in gene silencing by miRNA","type":"exact"},{"name":"down-regulation of translation involved in gene silencing by miRNA","type":"exact"},{"name":"downregulation of translation involved in gene silencing by miRNA","type":"exact"},{"name":"gene silencing by miRNA, negative regulation of translation","type":"exact"},{"name":"inhibition of translation involved in gene silencing by miRNA","type":"narrow"},{"name":"miRNA mediated inhibition of translation","type":"exact"},{"name":"miRNA-mediated gene silencing, negative regulation of translation","type":"related"},{"name":"negative regulation of translation involved in gene silencing by microRNA","type":"exact"}],"termid":"GO:0035278"}


id: FYPO:0004140
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of glutathione (GSH) measured in a cell that is subject to nitrogen starvation is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell","termid":"FYPO:0000990"},{"relation_name":"is_a","term_name":"altered level of substance in cell during nitrogen starvation","termid":"FYPO:0004139"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular glutathione level during nitrogen starvation","synonyms":[{"name":"increased cellular GSH level during nitrogen starvation","type":"exact"},{"name":"increased cellular L-gamma-glutamyl-L-cysteinylglycine level during nitrogen starvation","type":"exact"},{"name":"increased cellular glutathione level during nitrogen depletion","type":"exact"},{"name":"increased cellular glutathione level during nitrogen deprivation","type":"exact"},{"name":"increased cellular reduced glutathione level during nitrogen starvation","type":"exact"},{"name":"increased glutathione accumulation during nitrogen starvation","type":"related"}],"termid":"FYPO:0004140"}


id: GO:0070472
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of uterine smooth muscle contraction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of smooth muscle contraction","termid":"GO:0006940"},{"relation_name":"regulates","term_name":"uterine smooth muscle contraction","termid":"GO:0070471"}],"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 uterine smooth muscle contraction","synonyms":[{"name":"regulation of myometrial contraction","type":"exact"},{"name":"regulation of myometrial smooth muscle contraction","type":"exact"},{"name":"regulation of myometrium contraction","type":"exact"}],"termid":"GO:0070472"}


id: PBO:0016549
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by frog X-MAPK","termid":"PBO:0016549"}


id: PBO:0000202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcipressin (predicted)","termid":"PBO:0000202"}


id: PBO:0042044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 97","termid":"PBO:0042044"}


id: MONDO:1011423
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Complement component 6 deficiency that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement component 6 deficiency, non-human animal","secondary_identifiers":["OMIA:001624"],"synonyms":[{"name":"C6 deficiency","type":"exact"}],"termid":"MONDO:1011423","xrefs":{"Monarch":{"xref_id":"1011423"}}}


id: PATO:0000563
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000563 relative size value (obsolete PATO:0000563)","termid":"PATO:0000563"}


id: PBO:0073731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 1 member 1","termid":"PBO:0073731"}


id: PBO:0001892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human AMMECR1 homolog","termid":"PBO:0001892"}


id: MONDO:0011327
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuronal intranuclear inclusion disease (NIID) is a very rare multisystem neurodegenerative disorder characterized by the presence of eosinophilic intranuclear inclusions in neuronal and glial cells, and neuronal loss.","definition_xrefs":["Orphanet:2289"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"hereditary dementia","termid":"MONDO:0015547"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"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":"neuronal intranuclear inclusion disease","secondary_identifiers":["MEDGEN:355075","NCIT:C122655","DOID:0081294","GARD:3971","icd11.foundation:693937860","MESH:C537395","OMIM:603472","SCTID:715437003","UMLS:C1863843"],"synonyms":[{"name":"Niid","type":"related"},{"name":"neuronal intranuclear hyaline inclusion disease","type":"related"},{"name":"neuronal intranuclear inclusion disease","type":"exact"}],"termid":"MONDO:0011327","xrefs":{"Monarch":{"xref_id":"0011327"}}}


id: GO:0016972
data:
  {"annotated_genes":["SJAG_03992","SJAG_01647","SJAG_02489","SJAG_00196","SJAG_02827"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97998,110283,114228],"is_not":false,"summary":null,"term":"GO:0016972"},{"annotations":[96639,102672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016971"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 R'C(R)SH + O2 = R'C(R)S-S(R)CR' + 2 H2O2.","definition_xrefs":["RHEA:17357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disulfide oxidoreductase activity","termid":"GO:0015036"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor","termid":"GO:0016670"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00196":null,"SJAG_01647":null,"SJAG_02489":null,"SJAG_02827":null,"SJAG_03992":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0015036"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0015036","GO:0003824"],"is_obsolete":false,"name":"thiol oxidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["UM-BBD_reactionID:r1293","EC:1.8.3.2","MetaCyc:THIOL-OXIDASE-RXN"],"synonyms":[{"name":"sulfhydryl oxidase activity","type":"related"},{"name":"thiol:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0016972","terms_by_termid":{"GO:0016971":null,"GO:0016972":null}}


id: GO:0009734
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated by the binding of the plant hormone auxin to a receptor, and ending with modulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:16990790","GOC:mah","GOC:sm","PMID:18647826"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone-mediated signaling pathway","termid":"GO:0009755"},{"relation_name":"part_of","term_name":"cellular response to auxin stimulus","termid":"GO:0071365"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"auxin-activated signaling pathway","synonyms":[{"name":"auxin mediated signaling pathway","type":"related"},{"name":"auxin mediated signalling","type":"exact"},{"name":"auxin signal transduction","type":"exact"},{"name":"auxin signaling","type":"exact"},{"name":"auxin-regulated transcription","type":"related"}],"termid":"GO:0009734"}


id: MONDO:0044808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete early onset primary dystonia (obsolete MONDO:0044808)","secondary_identifiers":["NANDO:1200512"],"termid":"MONDO:0044808","xrefs":{"Monarch":{"xref_id":"0044808"}}}


id: GO:0051660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the centrosome to a specific location.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"centrosome localization","termid":"GO:0051642"},{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"is_a","term_name":"establishment of organelle localization","termid":"GO:0051656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"establishment of centrosome localization","synonyms":[{"name":"centrosome positioning","type":"exact"},{"name":"establishment of centrosome localisation","type":"exact"}],"termid":"GO:0051660"}


id: PBO:0034751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cohesin loading/unloading factor (WAPL) Wpl1","termid":"PBO:0034751"}


id: PBO:0058769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6893","termid":"PBO:0058769"}


id: GO:0072464
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that occurs in response to signals generated as a result of meiotic spindle assembly checkpoint signaling.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to meiotic cell cycle checkpoint signaling","termid":"GO:0072410"},{"relation_name":"is_a","term_name":"response to spindle assembly checkpoint signaling","termid":"GO:0072485"}],"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 meiotic spindle assembly checkpoint signaling","synonyms":[{"name":"meiotic spindle assembly checkpoint effector process","type":"exact"},{"name":"response to signal involved in meiotic spindle assembly checkpoint","type":"exact"}],"termid":"GO:0072464"}


id: SO:0000129
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is silenced by DNA methylation.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"silenced_by_DNA_methylation","termid":"SO:0000895"},{"relation_name":"is_a","term_name":"gene_silenced_by_DNA_modification","termid":"SO:0000128"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene_silenced_by_DNA_methylation","synonyms":[{"name":"gene silenced by DNA methylation","type":"exact"},{"name":"methylation-silenced gene","type":"exact"}],"termid":"SO:0000129"}


id: PBO:0044256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X3-C motif chemokine ligand 1","termid":"PBO:0044256"}


id: PBO:0044997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diaphanous related formin 3","termid":"PBO:0044997"}


id: PBO:0051151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-30-5","termid":"PBO:0051151"}


id: PBO:0003632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Fcf1 (predicted)","termid":"PBO:0003632"}


id: PR:Q9C1W5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitochondrial import inner membrane translocase subunit Tim16 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12388:SF0","PRO:DNx","OMA:SCHPO02627"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial import inner membrane translocase subunit tim16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC713.10","secondary_identifiers":["UniProtKB:Q9C1W5"],"synonyms":[{"name":"Spom972h-PAM16","type":"exact"},{"name":"presequence translocated-associated motor subunit pam16 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9C1W5"}


id: GO:0106025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of onset of pupariation.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of pupariation","termid":"GO:0106023"},{"relation_name":"positively_regulates","term_name":"pupariation","termid":"GO:0035073"}],"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 pupariation","termid":"GO:0106025"}


id: PBO:0012594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome complex subunit beta 1 Pre3 (predicted)","termid":"PBO:0012594"}


id: GO:0000704
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the removal of pyrimidine dimers by removing the 5' pyrimidine of the dimer by cleaving the N-C1' glycosidic bond between the 5' pyrimidine of the dimer and the deoxyribose sugar. The reaction releases the 5' pyrimidine of the dimer and leaves an apurinic (AP) site. The reaction involves the formation of a covalent enzyme substrate intermediate. Release of the enzyme and free base by a beta-elimination or a beta, gamma-elimination mechanism results in the cleavage of the DNA backbone 3' of the apyrimidinic (AP) site.","definition_xrefs":["PMID:9224623","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA N-glycosylase activity","termid":"GO:0019104"}],"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"},{"rel_name":"is_a","termid":"GO:0140097"}],"interesting_parent_ids":["GO:0003674","GO:0140097","GO:0016798","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"pyrimidine dimer DNA N-glycosylase activity","termid":"GO:0000704"}


id: MONDO:1010213
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chronic monocytic leukemia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukemia, non-human animal","termid":"MONDO:0700100"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic monocytic leukemia, non-human animal","secondary_identifiers":["OMIA:001573"],"termid":"MONDO:1010213","xrefs":{"Monarch":{"xref_id":"1010213"}}}


id: PBO:0056756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase like 8 pseudogene 1","termid":"PBO:0056756"}


id: GO:0051104
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The re-formation of a broken phosphodiester bond in the DNA backbone, carried out by DNA ligase, that contributes to DNA-dependent DNA replication.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA-dependent DNA replication DNA ligation (obsolete GO:0051104)","synonyms":[{"name":"DNA ligation during DNA-dependent DNA replication","type":"related"},{"name":"DNA ligation involved in DNA-dependent DNA replication","type":"exact"}],"termid":"GO:0051104"}


id: PBO:0058771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6895","termid":"PBO:0058771"}


id: GO:0070487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The adhesion of one monocyte to one or more other monocytes via adhesion molecules.","definition_xrefs":["PMID:12972508","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte aggregation","termid":"GO:0070486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"monocyte aggregation","synonyms":[{"name":"mononuclear phagocyte aggregation","type":"exact"}],"termid":"GO:0070487"}


id: PBO:0072475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 4","termid":"PBO:0072475"}


id: MONDO:0008259
data:
  {"annotated_genes":["SJAG_02231"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84543],"is_not":false,"summary":null,"term":"MONDO:0008259"}]},"cv_name":"mondo","definition":"Familial spontaneous pneumothorax is a rare, genetic pulmonary disease characterized by the uni- or bilateral accumulation of air in the pleural cavity in persons with a positive family history and no underlying lung disease or previous chest trauma. Patients typically present dyspnea associated with acute onset of sharp and steady pleutiric chest pain of variable severity (which resolves within 24h even though pneumothorax is still present). Reflex tachycardia and/or respiratory or circulatory compromise may be observed. Other syndromes (e.g. Birt-Hogg-Dube, Marfan or Ehlers-Danlos syndromes) may be associated.","definition_xrefs":["Orphanet:2903"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pneumothorax","termid":"MONDO:0002076"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02231":null},"genotype_count":0,"is_obsolete":false,"name":"familial spontaneous pneumothorax","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:173600","MESH:C566795","icd11.foundation:319022944","MEDGEN:357445","DOID:0080218","UMLS:C1868193","SCTID:715219001","GARD:4997"],"synonyms":[{"name":"Psp","type":"related"},{"name":"pneumothorax, primary spontaneous","type":"related"},{"name":"primary spontaneous pneumothorax","type":"related"},{"name":"spontaneous pneumothorax","type":"related"}],"termid":"MONDO:0008259","terms_by_termid":{"MONDO:0008259":null},"xrefs":{"Monarch":{"xref_id":"0008259"}}}


id: GO:0071634
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of production of transforming growth factor-beta.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"transforming growth factor beta production","termid":"GO:0071604"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of transforming growth factor beta production","secondary_identifiers":["GO:2001201"],"synonyms":[{"name":"regulation of TGF-B production","type":"exact"},{"name":"regulation of TGF-beta production","type":"exact"},{"name":"regulation of TGFB production","type":"exact"},{"name":"regulation of TGFbeta production","type":"exact"},{"name":"regulation of transforming growth factor-beta production","type":"exact"},{"name":"regulation of transforming growth factor-beta secretion","type":"narrow"}],"termid":"GO:0071634"}


id: PBO:0015255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sir antagonist, ubiquitin-protein ligase E3","termid":"PBO:0015255"}


id: PBO:0028441
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_galactose_level_in_glycoprotein_glycan","termid":"PBO:0028441"}


id: GO:2000350
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of signaling via the CD40 signaling pathway.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of CD40 signaling pathway","termid":"GO:2000348"},{"relation_name":"positively_regulates","term_name":"CD40 signaling pathway","termid":"GO:0023035"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of CD40 signaling pathway","synonyms":[{"name":"positive regulation of CD40 signalling pathway","type":"exact"}],"termid":"GO:2000350"}


id: PBO:0057411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548m","termid":"PBO:0057411"}


id: FYPO:0002376
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during a cellular response to osmotic stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during vegetative growth","termid":"FYPO:0001838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0002274","FYPO:0000002","FYPO:0001985","FYPO:0002494"],"is_obsolete":false,"name":"decreased protein phosphorylation during cellular response to osmotic stress","synonyms":[{"name":"decreased phosphorylation during cellular response to osmotic stress","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to osmotic stress during mitotic cell cycle","type":"related"},{"name":"decreased protein phosphorylation during cellular response to osmotic stress during vegetative growth","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to osmotic stress","type":"exact"}],"termid":"FYPO:0002376"}


id: GO:0016732
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which an iron-sulfur protein acts as a hydrogen or electron donor and reduces dinitrogen.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on iron-sulfur proteins as donors","termid":"GO:0016730"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"oxidoreductase activity, acting on iron-sulfur proteins as donors, dinitrogen as acceptor","secondary_identifiers":["EC:1.18.6.-"],"termid":"GO:0016732"}


id: PBO:0068181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 488","termid":"PBO:0068181"}


id: FYPO:0001691
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 paraquat.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0000003","FYPO:0002058","FYPO:0000257","FYPO:0002057","FYPO:0002060"],"is_obsolete":false,"name":"normal growth on paraquat","synonyms":[{"name":"normal cell population growth in presence of paraquat","type":"exact"},{"name":"normal cell population growth on paraquat","type":"exact"},{"name":"normal cellular response to paraquat","type":"related"},{"name":"normal vegetative cell population growth on paraquat","type":"exact"}],"termid":"FYPO:0001691"}


id: MONDO:0012943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the IDH3B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"IDH3B-related retinopathy","termid":"MONDO:0800393"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736","MONDO:0005328"],"is_obsolete":false,"name":"retinitis pigmentosa 46","secondary_identifiers":["UMLS:C2675496","ICD10CM:H35.5","DOID:0110409","MESH:C567249","OMIM:612572","GARD:15571","MEDGEN:382614"],"synonyms":[{"name":"IDH3B retinitis pigmentosa","type":"exact"},{"name":"RP46","type":"exact"},{"name":"retinitis pigmentosa 46","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in IDH3B","type":"exact"},{"name":"retinitis pigmentosa type 46","type":"exact"},{"name":"retinitis pigmentosa, autosomal recessive, Idh3B-related","type":"related"}],"termid":"MONDO:0012943","xrefs":{"Monarch":{"xref_id":"0012943"}}}


id: PBO:0068034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 339","termid":"PBO:0068034"}


id: PBO:0070174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 88 pseudogene","termid":"PBO:0070174"}


id: PBO:0005131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma tubulin complex subunit Alp16","termid":"PBO:0005131"}


id: GO:0141144
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont damages or impairs host neutrophil extracellular traps. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:25605868","PMID:16488875","PMID:21231972"],"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 disruption of host neutrophil extracellular traps","synonyms":[{"name":"symbiont-mediated perturbation of host neutrophil extracellular traps","type":"exact"}],"termid":"GO:0141144"}


id: PBO:0031566
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-catalytic_activity_phenotype","termid":"PBO:0031566"}


id: PBO:0082232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-glucosidase; specificity for isomaltose, maltose, and palatinose, but not alpha-methylglucoside; most distant member of the IMA isomaltase family, but with similar catalytic properties as Ima1p and Ima2p; not required for isomaltose utilization, but Ima5p overexpression allows the ima1 null mutant to grow on isomaltose; can cleave alpha-1,3 linkage of nigerose and turanose and alpha-1,5 linkage of leucrose and is very sensitive to temperature in vitro","termid":"PBO:0082232"}


id: MONDO:0859280
data:
  {"annotated_genes":["SJAG_02651","SJAG_01617","SJAG_00192","SJAG_02162"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85402,85403,85404,85405],"is_not":false,"summary":null,"term":"MONDO:0859280"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00192":null,"SJAG_01617":null,"SJAG_02162":null,"SJAG_02651":null},"genotype_count":0,"is_obsolete":false,"name":"developmental delay, hypotonia, and impaired language","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620012","UMLS:C5774202","DOID:0070420","MEDGEN:1823975"],"termid":"MONDO:0859280","terms_by_termid":{"MONDO:0859280":null},"xrefs":{"Monarch":{"xref_id":"0859280"}}}


id: PBO:0070700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 4","termid":"PBO:0070700"}


id: PBO:0082920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytochrome c, isoform 1; also known as iso-1-cytochrome c; electron carrier of mitochondrial intermembrane space that transfers electrons from ubiquinone-cytochrome c oxidoreductase to cytochrome c oxidase during cellular respiration; CYC1 has a paralog, CYC7, that arose from the whole genome duplication; human homolog CYC1 can complement yeast null mutant; mutations in human CYC1 cause insulin-responsive hyperglycemia","termid":"PBO:0082920"}


id: GO:1902348
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 strigolactone stimulus.","definition_xrefs":["PMID:23893171","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"},{"relation_name":"is_a","term_name":"cellular response to organic cyclic compound","termid":"GO:0071407"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to strigolactone","termid":"GO:1902347"}],"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 strigolactone","synonyms":[{"name":"cellular response to strigolactone analog GR24","type":"related"}],"termid":"GO:1902348"}


id: PBO:0018203
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calmodulin-dependent Kinase Kinase","termid":"PBO:0018203"}


id: FYPO:0000941
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the mitotic spindle pole body does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000934"},{"relation_name":"is_a","term_name":"abnormal protein localization to mitotic spindle pole body","termid":"FYPO:0000939"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"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:0005447","FYPO:0000002","FYPO:0001320","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to mitotic spindle pole body","synonyms":[{"name":"abolished protein localization to spindle pole body during mitotic cell cycle","type":"related"},{"name":"protein absent from mitotic spindle pole body","type":"related"},{"name":"protein localisation to mitotic spindle pole body abolished","type":"exact"},{"name":"protein localization to mitotic SPB abolished","type":"exact"},{"name":"protein localization to mitotic spindle pole body abolished","type":"exact"},{"name":"protein localization to spindle pole body abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0000941"}


id: PBO:0040446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase phospholipid transporting 9B (putative)","termid":"PBO:0040446"}


id: PBO:0090881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S9","termid":"PBO:0090881"}


id: PBO:0029728
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_1,3-beta-D-glucan_synthase_activity_during_growth_on_aculeacin_A","termid":"PBO:0029728"}


id: GO:0060485
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a mesenchymal tissue over time, from its formation to the mature structure. A mesenchymal tissue is made up of loosely packed stellate cells.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue development","termid":"GO:0009888"},{"relation_name":"part_of","term_name":"animal organ development","termid":"GO:0048513"}],"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":"mesenchyme development","synonyms":[{"name":"mesenchymal development","type":"exact"}],"termid":"GO:0060485"}


id: PBO:0049258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma-secretase activating protein","termid":"PBO:0049258"}


id: PBO:0087021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 40S subunit protein S0A; required for maturation of 18S rRNA along with Rps0Bp; deletion of either RPS0 gene reduces growth rate, deletion of both genes is lethal; homologous to human ribosomal protein SA and bacterial S2; RPS0A has a paralog, RPS0B, that arose from the whole genome duplication;","termid":"PBO:0087021"}


id: PBO:0088077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-specific protease that cleaves Ub-protein fusions; interacts with cofactor Bre5p to regulate transport between ER and Golgi, deubiquitinating COPII and COPI proteins, Sec23p and Sec27p; mediates steady-state retention of Golgi membrane proteins with Bre5p; phosphorylation (S695) by Hog1p regulates transcriptional activation by osmostress; inhibits Ras/PKA signaling through Ira2p; inhibits silencing; role in ribophagy; protein abundance increases in response to DNA replication stress","termid":"PBO:0088077"}


id: MONDO:0035941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality","termid":"MONDO:0035605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)","secondary_identifiers":["Orphanet:585918","NCIT:C80332","GARD:22343"],"synonyms":[{"name":"B Lymphoblastic Leukemia/Lymphoma with t(v;11q23.3); KMT2A Rearranged","type":"exact"},{"name":"B lymphoblastic leukaemia lymphoma with t(v;11q23); MLL rearranged","type":"exact"},{"name":"B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged","type":"exact"}],"termid":"MONDO:0035941","xrefs":{"Monarch":{"xref_id":"0035941"}}}


id: PBO:0029720
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-bent_mitotic_spindle","termid":"PBO:0029720"}


id: PBO:0114425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ciliary microtubule inner protein 7","termid":"PBO:0114425"}


id: GO:0004529
data:
  {"annotated_genes":["SJAG_05280","SJAG_02818","SJAG_00377","SJAG_02908","SJAG_05373","SJAG_02298","SJAG_01173","SJAG_01163","SJAG_03734","SJAG_01648","SJAG_04410","SJAG_01832"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104702,108571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008296"},{"annotations":[87910,92506,96629],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035312"},{"annotations":[115128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033699"},{"annotations":[88067,109416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008311"},{"annotations":[107225,96632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051908"},{"annotations":[100636,88070,106824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008310"},{"annotations":[96634,111039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045145"}]},"cv_name":"molecular_function","definition":"Catalysis of the sequential cleavage of mononucleotides from a free 5' or 3' terminus of a DNA molecule.","definition_xrefs":["GOC:mah","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exonuclease activity","termid":"GO:0004527"},{"relation_name":"is_a","term_name":"DNA nuclease activity","termid":"GO:0004536"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00377":null,"SJAG_01163":null,"SJAG_01173":null,"SJAG_01648":null,"SJAG_01832":null,"SJAG_02298":null,"SJAG_02818":null,"SJAG_02908":null,"SJAG_03734":null,"SJAG_04410":null,"SJAG_05280":null,"SJAG_05373":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004527"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016787","GO:0004527","GO:0016788","GO:0003824","GO:0140097","GO:0003674"],"is_obsolete":false,"name":"DNA exonuclease activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0004529","terms_by_termid":{"GO:0008296":null,"GO:0008310":null,"GO:0008311":null,"GO:0033699":null,"GO:0035312":null,"GO:0045145":null,"GO:0051908":null}}


id: PBO:0065618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 phosphatase activator","termid":"PBO:0065618"}


id: PBO:0049817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase 9","termid":"PBO:0049817"}


id: MONDO:0020414
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"aortic arch defects","termid":"MONDO:0015236"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent fifth aortic arch","secondary_identifiers":["icd11.foundation:82536098","GARD:19636","Orphanet:99076","MEDGEN:576728","UMLS:C0345066"],"termid":"MONDO:0020414","xrefs":{"Monarch":{"xref_id":"0020414"}}}


id: PBO:0083368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps uncharacterized ORF YDL086W; identified by gene-trapping, microarray expression analysis, and genome-wide homology searching","termid":"PBO:0083368"}


id: PBO:0087526
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 the oxidation of isocitrate to alpha-ketoglutarate in the TCA cycle; phosphorylated","termid":"PBO:0087526"}


id: PBO:0062968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A) binding protein cytoplasmic 1 pseudogene 11","termid":"PBO:0062968"}


id: GO:0047038
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-arabinitol + NAD+ = D-ribulose + H+ + NADH.","definition_xrefs":["EC:1.1.1.250","RHEA:17389"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"D-arabinitol 2-dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R07134","MetaCyc:1.1.1.250-RXN"],"synonyms":[{"name":"D-arabinitol 2-dehydrogenase (ribulose-forming) activity","type":"related"},{"name":"D-arabinitol:NAD+ 2-oxidoreductase (D-ribulose-forming)","type":"related"}],"termid":"GO:0047038"}


id: PBO:0072698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RUS family member 1","termid":"PBO:0072698"}


id: PBO:0077826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TP53 target 3 family member E","termid":"PBO:0077826"}


id: GO:1990271
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Combining with anti-Mullerian hormone to initiate a change in cell activity.","definition_xrefs":["GOC:hjd","PMID:23624077"],"gene_count":0,"genotype_count":0,"name":"obsolete anti-Mullerian hormone (obsolete GO:1990271)","synonyms":[{"name":"anti-Mullerian hormone","type":"exact"}],"termid":"GO:1990271"}


id: PBO:0017043
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae FEN2","termid":"PBO:0017043"}


id: PBO:0063297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin gamma subfamily C, 4","termid":"PBO:0063297"}


id: PBO:0049024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 3","termid":"PBO:0049024"}


id: GO:0038131
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a neuregulin, a member of the EGF family of growth factors, and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["PMID:20672328","GOC:signaling","GOC:bf","PMID:16460914"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"}],"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:0003674","GO:0038023"],"is_obsolete":false,"name":"neuregulin receptor activity","synonyms":[{"name":"NRG receptor activity","type":"exact"},{"name":"NRG1 receptor activity","type":"narrow"},{"name":"NRG2 receptor activity","type":"narrow"}],"termid":"GO:0038131"}


id: GO:0018062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of an N-terminal peptidyl-tryptophan residue to form peptidyl-N2-succinyl-L-tryptophan.","definition_xrefs":["RESID:AA0130"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-tryptophan succinylation (obsolete GO:0018062)","termid":"GO:0018062"}


id: MONDO:0012822
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"colorectal cancer","termid":"MONDO:0005575"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colorectal cancer, susceptibility to, 6","secondary_identifiers":["UMLS:C2677121","MEDGEN:436865","OMIM:612231"],"synonyms":[{"name":"CRCS6","type":"exact"},{"name":"colorectal cancer, susceptibility to, 6","type":"exact"},{"name":"colorectal cancer, susceptibility to, on chromosome 8Q23","type":"related"}],"termid":"MONDO:0012822","xrefs":{"Monarch":{"xref_id":"0012822"}}}


id: PR:Q9URY1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppk16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9URY1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine-protein kinase ppk16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC890.03","synonyms":[{"name":"Spom972h-ppk16","type":"exact"},{"name":"meiotically up-regulated gene 92 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9URY1"}


id: PBO:0074770
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 3C","termid":"PBO:0074770"}


id: PBO:0070807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 37","termid":"PBO:0070807"}


id: GO:0016823
data:
  {"annotated_genes":["SJAG_00493"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018773"},{"annotations":[106247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047621"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any acid carbon-carbon bond in a ketonic substance, a substance containing a keto (C=O) group.","definition_xrefs":["EC:3.7.1.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-carbon bonds","termid":"GO:0016822"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00493":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":"hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0016823","terms_by_termid":{"GO:0018773":null,"GO:0047621":null}}


id: FYPO:0007015
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at the 3' ends of tRNA genes is increased.","definition_xrefs":["PomBase:mah","PMID:31294478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to chromatin at tRNA genes","termid":"FYPO:0004033"},{"relation_name":"is_a","term_name":"increased protein localization to chromatin at 3' end of RNA polymerase III-transcribed genes","termid":"FYPO:0007734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased protein localization to chromatin at 3' end of tRNA genes","synonyms":[{"name":"increased protein localisation to chromatin at 3' end of tRNA genes","type":"exact"},{"name":"increased protein localization to chromatin at 3' end of tRNA genes during mitotic cell cycle","type":"related"},{"name":"increased protein localization to chromatin at 3' end of tRNA genes during vegetative growth","type":"exact"},{"name":"increased protein localization to chromatin at 3' end of transfer RNA genes","type":"exact"},{"name":"increased protein localization to chromatin at tRNA genes at 3' end","type":"exact"}],"termid":"FYPO:0007015"}


id: GO:0150092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that modulates synaptic scaling. Synaptic scaling is a form of synaptic plasticity, which entails uniform adjustments in the strength of all synapses on a cell in response to prolonged changes in the electrical activity of the cell.","definition_xrefs":["PMID:16547515","GOC:bc","GOC:aruk","PMID:14735113","PMID:14630218"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synaptic plasticity","termid":"GO:0048167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of synaptic scaling","synonyms":[{"name":"homeostatic synaptic scaling","type":"related"},{"name":"regulation of homeostatic synaptic scaling","type":"related"}],"termid":"GO:0150092"}


id: GO:0097183
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex that contains protein C inhibitor (SERPINA5) and coagulation factor XI (F11); formation of the complex inhibits the serine protease activity of coagulation factor XI.","definition_xrefs":["GOC:ans","PMID:2844223"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine protease inhibitor complex","termid":"GO:0097180"}],"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":"protein C inhibitor-coagulation factor XI complex","synonyms":[{"name":"PCI-coagulation factor XI complex","type":"exact"},{"name":"SERPINA5-coagulation factor XI complex","type":"exact"},{"name":"plasma serine protease inhibitor-coagulation factor XI complex","type":"exact"},{"name":"protein C inhibitor-F11 complex","type":"exact"},{"name":"serpin A5-coagulation factor XI complex","type":"exact"}],"termid":"GO:0097183"}


id: PBO:0059291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L42 pseudogene 6","termid":"PBO:0059291"}


id: GO:0097198
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by addition of three methyl groups to lysine at position 36 of the histone.","definition_xrefs":["GOC:se","PMID:17948059"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K36 trimethylation (obsolete GO:0097198)","termid":"GO:0097198"}


id: GO:0008982
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + sugar(out) = protein histidine + sugar phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transmembrane transporter activity","termid":"GO:0015144"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"active transmembrane transporter activity","termid":"GO:0022804"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0022857","GO:0005215","GO:0003824"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","secondary_identifiers":["GO:0015455","GO:0015456","TC:4.A"],"synonyms":[{"name":"PEP--sugar phosphotransferase enzyme II activity","type":"exact"},{"name":"PEP-dependent phosphotransferase enzyme II","type":"related"},{"name":"PTS permease activity","type":"related"},{"name":"PTS transporter","type":"related"},{"name":"enzyme II of the phosphotransferase system","type":"related"},{"name":"phosphoenolpyruvate-sugar phosphotransferase enzyme II","type":"related"},{"name":"phosphohistidinoprotein-hexose phosphotransferase activity","type":"related"},{"name":"phosphoprotein factor-hexose phosophotransferase activity","type":"related"},{"name":"phosphotransfer-driven group translocator","type":"broad"},{"name":"protein-Np-phosphohistidine-sugar phosphotransferase activity","type":"exact"}],"termid":"GO:0008982"}


id: PBO:0017934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA transmembrane transporter (predicted)","termid":"PBO:0017934"}


id: PBO:0073159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC61G divergent transcript","termid":"PBO:0073159"}


id: GO:0080033
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 nitrite stimulus.","definition_xrefs":["PMID:17951451","GOC:dhl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"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 nitrite","termid":"GO:0080033"}


id: PBO:0079018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-undetermined (NNN) 1-1","termid":"PBO:0079018"}


id: MOD:01375
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-leucine residue to a (2S,4R)-4,5-dihydroxyleucine.","definition_xrefs":["PubMed:6010785","RESID:AA0445","ChEBI:141823","PubMed:6893271"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dihydroxylated leucine","termid":"MOD:01412"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(2S,4R)-4,5-dihydroxyleucine","synonyms":[{"name":"(2S,4R)-2-amino-4,5-dihydroxy-4-methylpentanoic acid","type":"exact"},{"name":"(2S,4R)-4,5-dihydroxyleucine","type":"exact"},{"name":"(4R)-4,5-dihydroxyleucine","type":"exact"},{"name":"MOD_RES (4R)-4,5-dihydroxyleucine","type":"exact"},{"name":"gamma,delta-dihydroxyleucine","type":"exact"}],"termid":"MOD:01375"}


id: PBO:0027566
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_mitotic_spindle_microtubules_protruding_beyond_spindle_pole_body","termid":"PBO:0027566"}


id: GO:0043756
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: adenosylcobinamide + H2O = (R)-1-aminopropan-2-ol + adenosylcobyrate.","definition_xrefs":["RHEA:23504","EC:3.5.1.90"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"adenosylcobinamide hydrolase activity","secondary_identifiers":["KEGG_REACTION:R05226","MetaCyc:R346-RXN"],"synonyms":[{"name":"AdoCbi amidohydrolase activity","type":"related"},{"name":"AdoCbi hydrolase activity","type":"related"},{"name":"CbiZ","type":"related"},{"name":"adenosylcobinamide amidohydrolase activity","type":"related"}],"termid":"GO:0043756"}


id: PBO:0039902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGEF4 antisense RNA 1","termid":"PBO:0039902"}


id: PBO:0069635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 912, pseudogene","termid":"PBO:0069635"}


id: PBO:0014276
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIBoflavin","termid":"PBO:0014276"}


id: GO:0160017
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of platelet rolling.","definition_xrefs":["GO_REF:0000058","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heterotypic cell-cell adhesion","termid":"GO:0034114"},{"relation_name":"regulates","term_name":"platelet rolling","termid":"GO:0160015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"regulation of platelet rolling","termid":"GO:0160017"}


id: MONDO:0022908
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":"cutis gyratum acanthosis nigricans craniosynostosis","termid":"MONDO:0022908","xrefs":{"Monarch":{"xref_id":"0022908"}}}


id: PBO:0000563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin C-terminal hydrolase, poly(A)-specific ribonuclease complex subunit Pan2 (predicted)","termid":"PBO:0000563"}


id: GO:0004497
data:
  {"annotated_genes":["SJAG_03018","SJAG_04032","SJAG_00459","SJAG_04608","SJAG_03750","SJAG_02285","SJAG_04913","SJAG_04000","SJAG_00370"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008682"},{"annotations":[102724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106364"},{"annotations":[98354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000254"},{"annotations":[95582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019135"},{"annotations":[91316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080132"},{"annotations":[112457],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004499"},{"annotations":[93621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031172"},{"annotations":[102726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016712"},{"annotations":[111259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004506"},{"annotations":[87992],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008398"}]},"cv_name":"molecular_function","definition":"Catalysis of the incorporation of one atom from molecular oxygen into a compound and the reduction of the other atom of oxygen to water.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity","termid":"GO:0016491"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00370":null,"SJAG_00459":null,"SJAG_02285":null,"SJAG_03018":null,"SJAG_03750":null,"SJAG_04000":null,"SJAG_04032":null,"SJAG_04608":null,"SJAG_04913":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"monooxygenase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5662662","Reactome:R-HSA-211962","Reactome:R-HSA-211948","Reactome:R-HSA-2161899","Reactome:R-HSA-9749986","Reactome:R-HSA-9753285","Reactome:R-HSA-9027042","Reactome:R-HSA-5605147","Reactome:R-HSA-5423678","Reactome:R-HSA-76397","Reactome:R-HSA-76472","Reactome:R-HSA-9027302","Reactome:R-HSA-215526","Reactome:R-HSA-9027043","Reactome:R-HSA-9756162","Reactome:R-HSA-9756138","Reactome:R-HSA-213175","Reactome:R-HSA-2161814","Reactome:R-HSA-212004","Reactome:R-HSA-211960","Reactome:R-HSA-76426","Reactome:R-HSA-9915997","Reactome:R-HSA-211929","Reactome:R-HSA-5662692","Reactome:R-HSA-211910","Reactome:R-HSA-2161940","Reactome:R-HSA-9027044","Reactome:R-HSA-76354","Reactome:R-HSA-211968","Reactome:R-HSA-5423664","Reactome:R-HSA-5423672","Reactome:R-HSA-5602295","Reactome:R-HSA-9756180","Reactome:R-HSA-9915971","Reactome:R-HSA-211991","Reactome:R-HSA-76475","Reactome:R-HSA-2161890","Reactome:R-HSA-9915992","Reactome:R-HSA-217258","Reactome:R-HSA-76373","Reactome:R-HSA-2161795","Reactome:R-HSA-76386","Reactome:R-HSA-76456","Reactome:R-HSA-76434","Reactome:R-HSA-212005","Reactome:R-HSA-9037761","Reactome:R-HSA-5602272","Reactome:R-HSA-9027321","Reactome:R-HSA-76466","Reactome:R-HSA-211959","Reactome:R-HSA-211919","Reactome:R-HSA-8865107","Reactome:R-HSA-9756169","Reactome:R-HSA-9018874","Reactome:R-HSA-211988","Reactome:R-HSA-5663050","Reactome:R-HSA-211882","Reactome:R-HSA-211924","Reactome:R-HSA-143468","Reactome:R-HSA-2162191","Reactome:R-HSA-5423647","Reactome:R-HSA-5602242","Reactome:R-HSA-76416","Reactome:R-HSA-9915993","Reactome:R-HSA-9750016","Reactome:R-HSA-211904","Reactome:R-HSA-156526"],"synonyms":[{"name":"hydroxylase activity","type":"related"}],"termid":"GO:0004497","terms_by_termid":{"GO:0000254":null,"GO:0004499":null,"GO:0004506":null,"GO:0008398":null,"GO:0008682":null,"GO:0016712":null,"GO:0019135":null,"GO:0031172":null,"GO:0080132":null,"GO:0106364":null}}


id: MONDO:0014488
data:
  {"annotated_genes":["SJAG_00092","SJAG_02012"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86870,86871],"is_not":false,"summary":null,"term":"MONDO:0014488"}]},"cv_name":"mondo","definition":"Any type 2 diabetes mellitus in which the cause of the disease is a mutation in the TBC1D4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"type 2 diabetes mellitus","termid":"MONDO:0005148"},{"relation_name":"is_a","term_name":"monogenic diabetes","termid":"MONDO:0015967"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00092":null,"SJAG_02012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005015","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"diabetes mellitus, noninsulin-dependent, 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:863620","OMIM:616087","UMLS:C4015183"],"synonyms":[{"name":"NIDDM5","type":"related"},{"name":"TBC1D4 type 2 diabetes mellitus","type":"exact"},{"name":"diabetes mellitus, noninsulin-dependent, 5","type":"exact"},{"name":"diabetes mellitus, noninsulin-dependent, type 5","type":"exact"},{"name":"type 2 diabetes mellitus caused by mutation in TBC1D4","type":"exact"}],"termid":"MONDO:0014488","terms_by_termid":{"MONDO:0014488":null},"xrefs":{"Monarch":{"xref_id":"0014488"}}}


id: MONDO:0015428
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Choroidal atrophy - alopecia is a very rare ectodermal dysplasia syndrome, characterized by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails.","definition_xrefs":["Orphanet:1433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"choroidal atrophy-alopecia syndrome","secondary_identifiers":["SCTID:720850008","UMLS:C2931026","GARD:3704","MESH:C535810","MEDGEN:419316"],"synonyms":[{"name":"Moloney syndrome","type":"exact"},{"name":"choroidal atrophy alopecia","type":"related"},{"name":"fine hair, absent/decreased lashes, absent/decreased eyebrows, visual loss-mild/suspected, dysplastic/thick/grooved toenails and fingernails","type":"related"},{"name":"regional choroidal atrophy and alopecia","type":"exact"}],"termid":"MONDO:0015428","xrefs":{"Monarch":{"xref_id":"0015428"}}}


id: PBO:0065101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKAR1B antisense RNA 2","termid":"PBO:0065101"}


id: GO:0010063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that induces or promotes trichoblast fate specification.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of trichoblast fate specification","termid":"GO:0010061"},{"relation_name":"is_a","term_name":"positive regulation of cell fate specification","termid":"GO:0042660"},{"relation_name":"is_a","term_name":"positive regulation of plant epidermal cell differentiation","termid":"GO:1903890"},{"relation_name":"positively_regulates","term_name":"trichoblast fate specification","termid":"GO:0010057"}],"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 trichoblast fate specification","synonyms":[{"name":"activation of trichoblast fate","type":"narrow"},{"name":"stimulation of trichoblast fate","type":"narrow"},{"name":"up regulation of trichoblast fate","type":"exact"},{"name":"up-regulation of trichoblast fate","type":"exact"},{"name":"upregulation of trichoblast fate","type":"exact"}],"termid":"GO:0010063"}


id: PBO:0028113
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_G418","termid":"PBO:0028113"}


id: PBO:0050667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family A (Hsp70) member 4 like","termid":"PBO:0050667"}


id: SO:0100018
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A polypeptide binding motif is a short (up to 20 amino acids) polypeptide region of biological interest that contains one or more amino acids experimentally shown to bind to a ligand.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biochemical_region_of_peptide","termid":"SO:0100001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"polypeptide_binding_motif","synonyms":[{"name":"binding","type":"related"},{"name":"polypeptide binding motif","type":"exact"}],"termid":"SO:0100018"}


id: GO:0032289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the wraps of cell membrane that constitute myelin are laid down around an axon by an oligodendrocyte in the central nervous system.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myelin assembly","termid":"GO:0032288"},{"relation_name":"part_of","term_name":"central nervous system myelination","termid":"GO:0022010"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"central nervous system myelin formation","synonyms":[{"name":"central nervous system myelin sheath formation","type":"exact"},{"name":"myelin formation in central nervous system","type":"exact"}],"termid":"GO:0032289"}


id: GO:0035906
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the descending aorta over time, from its initial formation to the mature structure. The descending aorta is the portion of the aorta in a two-pass circulatory system from the arch of aorta to the point where it divides into the common iliac arteries. In a two-pass circulatory system blood passes twice through the heart to supply the body once.","definition_xrefs":["UBERON:0001514","MA:0002571","GOC:bf","GOC:dgh","Wikipedia:Descending_aorta"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"aorta development","termid":"GO:0035904"}],"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":"descending aorta development","termid":"GO:0035906"}


id: GO:0030162
data:
  {"annotated_genes":["SJAG_01528","SJAG_01210","SJAG_00052","SJAG_02723","SJAG_02485","SJAG_01489","SJAG_01131","SJAG_00642","SJAG_03699","SJAG_01544","SJAG_00766","SJAG_02244","SJAG_00071","SJAG_03048","SJAG_04477","SJAG_00712","SJAG_00077","SJAG_00475"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905785"},{"annotations":[99364,96041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904293"},{"annotations":[106416,89914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032435"},{"annotations":[88460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905786"},{"annotations":[67795,65299,61238,66776,68139,66560],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901800"},{"annotations":[108351,111164,101872,116516,106124],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032436"},{"annotations":[89469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045862"},{"annotations":[114073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032434"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the hydrolysis of a peptide bond or bonds within a protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein metabolic process","termid":"GO:0051246"},{"relation_name":"regulates","term_name":"proteolysis","termid":"GO:0006508"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00052":null,"SJAG_00071":null,"SJAG_00077":null,"SJAG_00475":null,"SJAG_00642":null,"SJAG_00712":null,"SJAG_00766":null,"SJAG_01131":null,"SJAG_01210":null,"SJAG_01489":null,"SJAG_01528":null,"SJAG_01544":null,"SJAG_02244":null,"SJAG_02485":null,"SJAG_02723":null,"SJAG_03048":null,"SJAG_03699":null,"SJAG_04477":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of proteolysis","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"regulation of peptidolysis","type":"exact"}],"termid":"GO:0030162","terms_by_termid":{"GO:0032434":null,"GO:0032435":null,"GO:0032436":null,"GO:0045862":null,"GO:1901800":null,"GO:1904293":null,"GO:1905785":null,"GO:1905786":null}}


id: PR:Q9P7S7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nucleolar protein 58 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10894:SF0","PRO:DNx","OMA:SCHPO00338"],"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":"nucleolar protein 58 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23G3.06","secondary_identifiers":["UniProtKB:Q9P7S7"],"synonyms":[{"name":"Spom972h-NOP58","type":"exact"}],"termid":"PR:Q9P7S7"}


id: PBO:0056848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mahogunin ring finger 1","termid":"PBO:0056848"}


id: GO:0045663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of myoblast differentiation. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["GOC:go_curators","GOC:mtg_muscle","CL:0000056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of myoblast differentiation","termid":"GO:0045661"},{"relation_name":"positively_regulates","term_name":"myoblast differentiation","termid":"GO:0045445"}],"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 myoblast differentiation","synonyms":[{"name":"activation of myoblast differentiation","type":"narrow"},{"name":"stimulation of myoblast differentiation","type":"narrow"},{"name":"up regulation of myoblast differentiation","type":"exact"},{"name":"up-regulation of myoblast differentiation","type":"exact"},{"name":"upregulation of myoblast differentiation","type":"exact"}],"termid":"GO:0045663"}


id: PBO:0082330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase, putative RNA helicase of the DEAD-box family; component of 90S preribosome complex involved in production of 18S rRNA and assembly of 40S small ribosomal subunit; ATPase activity stimulated by association with Esf2p","termid":"PBO:0082330"}


id: PBO:0028220
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_mRNA_splicing,_via_spliceosome","termid":"PBO:0028220"}


id: FYPO:0001594
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of asparagine into the cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased amino acid import during vegetative growth","termid":"FYPO:0001360"},{"relation_name":"is_a","term_name":"abnormal asparagine import","termid":"FYPO:0001656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"decreased asparagine import","synonyms":[{"name":"decreased L-asparagine import","type":"exact"},{"name":"decreased L-asparagine import across plasma membrane","type":"exact"},{"name":"decreased asparagine import during mitotic cell cycle","type":"related"},{"name":"decreased asparagine import during vegetative growth","type":"exact"},{"name":"decreased asparagine import into cell","type":"exact"},{"name":"decreased asparagine uptake","type":"exact"},{"name":"reduced asparagine import","type":"exact"}],"termid":"FYPO:0001594"}


id: GO:0070689
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-threonine (the L-enantiomer of 2-amino-3-hydroxybutyric acid) to form the compound propionate.","definition_xrefs":["GOC:bf","GOC:mah","MetaCyc:PWY-5437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"threonine catabolic process","termid":"GO:0006567"},{"relation_name":"is_a","term_name":"propionate metabolic process","termid":"GO:0019541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0044248","GO:0006629","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"L-threonine catabolic process to propionate","synonyms":[{"name":"L-threonine breakdown to propionate","type":"exact"},{"name":"L-threonine catabolism to propionate","type":"exact"},{"name":"L-threonine degradation to propionate","type":"exact"},{"name":"threonine catabolic process to propionate","type":"broad"}],"termid":"GO:0070689"}


id: PBO:0071526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 29","termid":"PBO:0071526"}


id: MONDO:0007334
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant popliteal pterygium syndrome (AD-PPS) is a rare genetic malformative disorder characterized by cleft lip, with or without cleft palate, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail.","definition_xrefs":["Orphanet:1300"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome or malformation associated with head and neck malformations (obsolete MONDO:0015501)","termid":"MONDO:0015501"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"popliteal pterygium syndrome","termid":"MONDO:0017435"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant popliteal pterygium syndrome","secondary_identifiers":["SCTID:718222000","MEDGEN:1844082","GARD:3242","OMIM:119500","icd11.foundation:2069589860","UMLS:C5848052"],"synonyms":[{"name":"PPS","type":"related"},{"name":"cleft Lip/palate, paramedian mucous cysts of the Lower Lip, popliteal pterygium, digital and genital anomalies","type":"related"},{"name":"cleft lip/palate paramedian mucous cysts of the lower lip popliteal pterygium digital and genital anomalies","type":"related"},{"name":"facio-genito-popliteal syndrome","type":"broad"},{"name":"faciogenitopopliteal syndrome","type":"related"},{"name":"popliteal pterygium syndrome","type":"related"},{"name":"popliteal pterygium syndrome 1","type":"exact"},{"name":"popliteal pterygium syndrome, autosomal dominant","type":"exact"},{"name":"popliteal web syndrome","type":"exact"}],"termid":"MONDO:0007334","xrefs":{"Monarch":{"xref_id":"0007334"}}}


id: PBO:0070816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 46","termid":"PBO:0070816"}


id: PBO:0071865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 3","termid":"PBO:0071865"}


id: FYPO:0005555
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 cohesin loading is decreased during the mitotic cell cycle. Cohesin loading is the topological linking of a cohesin ring complex to chromatin.","definition_xrefs":["PomBase:mah","GO:0061780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of molecular function","termid":"FYPO:0000682"},{"relation_name":"is_a","term_name":"decreased protein localization to chromatin during vegetative growth","termid":"FYPO:0002909"},{"relation_name":"is_a","term_name":"abnormal cohesin loading","termid":"FYPO:0006479"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0000641","FYPO:0000002","FYPO:0000631","FYPO:0001320"],"is_obsolete":false,"name":"decreased mitotic cohesin loading","synonyms":[{"name":"decreased cohesin loading during mitotic cell cycle","type":"exact"},{"name":"decreased cohesin loading during vegetative growth","type":"exact"},{"name":"decreased mitotic cohesin association with chromatin","type":"exact"},{"name":"decreased mitotic cohesin localization to chromatin","type":"exact"},{"name":"reduced mitotic cohesin loading","type":"exact"}],"termid":"FYPO:0005555"}


id: GO:0008696
data:
  {"annotated_genes":["SJAG_02225"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105551],"is_not":false,"summary":null,"term":"GO:0008696"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-amino-4-deoxychorismate = 4-aminobenzoate + H+ + pyruvate.","definition_xrefs":["RHEA:16201","EC:4.1.3.38"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxo-acid-lyase activity","termid":"GO:0016833"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02225":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:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"4-amino-4-deoxychorismate lyase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:ADCLY-RXN","KEGG_REACTION:R05553"],"synonyms":[{"name":"4-amino-4-deoxychorismate pyruvate-lyase (4-aminobenzoate-forming)","type":"related"},{"name":"4-amino-4-deoxychorismate pyruvate-lyase activity","type":"related"},{"name":"ADC lyase activity","type":"related"},{"name":"aminodeoxychorismate lyase activity","type":"exact"},{"name":"enzyme X activity","type":"related"},{"name":"p-aminobenzoate synthetase","type":"related"},{"name":"para-aminobenzoic acid (PABA) synthase","type":"related"},{"name":"para-aminobenzoic acid synthase","type":"related"}],"termid":"GO:0008696","terms_by_termid":{"GO:0008696":null}}


id: PBO:0071772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein lateral stalk subunit P2 pseudogene 5","termid":"PBO:0071772"}


id: PBO:0053244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholysine phosphohistidine inorganic pyrophosphate phosphatase","termid":"PBO:0053244"}


id: PBO:0069837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1123, pseudogene","termid":"PBO:0069837"}


id: PBO:0084384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Low-affinity glucose transporter of the major facilitator superfamily; expression is induced by Hxk2p in the presence of glucose and repressed by Rgt1p when glucose is limiting; HXT1 has a paralog, HXT6, what arose from the whole genome duplication","termid":"PBO:0084384"}


id: PR:P31406
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A V-type proton ATPase catalytic subunit A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00670","PANTHER:PTHR15184:SF7","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":"V-type proton ATPase catalytic subunit A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC343.05","secondary_identifiers":["UniProtKB:P31406"],"synonyms":[{"name":"Spom972h-ATP6V1A","type":"exact"},{"name":"V-ATPase 67 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"V-ATPase subunit A (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"vacuolar proton pump subunit alpha (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P31406"}


id: PBO:0063064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pantothenate kinase 3","termid":"PBO:0063064"}


id: GO:0003045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulation of blood pressure mediated by detection of forces within the circulatory system.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure","termid":"GO:0003073"}],"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 systemic arterial blood pressure by physical factors","synonyms":[{"name":"blood pressure regulation by physical factors","type":"exact"}],"termid":"GO:0003045"}


id: PBO:0048332
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 43","termid":"PBO:0048332"}


id: PBO:0029615
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_vegetative_cell_with_normal_cell_shape","termid":"PBO:0029615"}


id: GO:0160073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a Casparian strip, a region of plant cell wall specialised to act as a seal to prevent back leakage of secreted material.","definition_xrefs":["PMID:28104889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"part_of","term_name":"plant-type cell wall assembly","termid":"GO:0071668"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0071554","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"Casparian strip assembly","synonyms":[{"name":"Casparian strip formation","type":"exact"}],"termid":"GO:0160073"}


id: PBO:0063092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAQR9 antisense RNA 1","termid":"PBO:0063092"}


id: PBO:0080911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta","termid":"PBO:0080911"}


id: PBO:0085995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; required for wild-type growth rate on galactose and mannose; localizes to COPI coated vesicles and the Golgi apparatus","termid":"PBO:0085995"}


id: PBO:0043424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclic nucleotide gated channel subunit alpha 2","termid":"PBO:0043424"}


id: PBO:0028602
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_level_during_cellular_response_to_glucose_starvation","termid":"PBO:0028602"}


id: GO:0102622
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: linuron + H2O = N,O-dimethylhydroxylamine + carbon dioxide + 3,4-dichloroaniline.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete linuron hydrolase activity (obsolete GO:0102622)","termid":"GO:0102622"}


id: MONDO:0020015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A rare form of cardiovascular disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare circulatory system disease (obsolete MONDO:0020015)","secondary_identifiers":["Orphanet:98028"],"synonyms":[{"name":"rare cardiovascular disease","type":"exact"}],"termid":"MONDO:0020015","xrefs":{"Monarch":{"xref_id":"0020015"}}}


id: PBO:0089539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane calcium ion transmembrane transporter","termid":"PBO:0089539"}


id: PBO:0040105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acylsphingosine amidohydrolase 1","termid":"PBO:0040105"}


id: PBO:0060264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYG1 exonuclease","termid":"PBO:0060264"}


id: PBO:0081961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zona pellucida binding protein","termid":"PBO:0081961"}


id: PBO:0045209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C4","termid":"PBO:0045209"}


id: PBO:0091683
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RecA-Like Protein","termid":"PBO:0091683"}


id: GO:0110023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cardiac muscle myoblast proliferation.","definition_xrefs":["GOC:BHF","GOC:BHF_miRNA","GOC:rph","PMID:26512644"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac muscle myoblast proliferation","termid":"GO:0110022"},{"relation_name":"is_a","term_name":"negative regulation of myoblast proliferation","termid":"GO:2000818"},{"relation_name":"negatively_regulates","term_name":"cardiac muscle myoblast proliferation","termid":"GO:0110021"}],"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 cardiac muscle myoblast proliferation","termid":"GO:0110023"}


id: MONDO:0043164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hydrocephalus","termid":"MONDO:0001150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"palmer pagon syndrome","secondary_identifiers":["MEDGEN:419886","Orphanet:2184","UMLS:C2931734","GARD:4199","MESH:C538107"],"synonyms":[{"name":"familial hydrocephalus with a low-insertion umbilicus","type":"related"},{"name":"hydrocephaly - low insertion umbilicus","type":"related"}],"termid":"MONDO:0043164","xrefs":{"Monarch":{"xref_id":"0043164"}}}


id: GO:0060189
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of protein desumoylation. Protein desumoylation is the process in which a SUMO protein (small ubiquitin-related modifier) is cleaved from its target protein.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein desumoylation","termid":"GO:0060188"},{"relation_name":"is_a","term_name":"positive regulation of protein modification by small protein conjugation or removal","termid":"GO:1903322"},{"relation_name":"positively_regulates","term_name":"protein desumoylation","termid":"GO:0016926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein desumoylation","termid":"GO:0060189"}


id: GO:1905917
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell differentiation involved in phenotypic switching.","definition_xrefs":["GOC:rph","PMID:25089138","GOC:BHF_miRNA","GOC:TermGenie","GO_REF:0000058","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of cell differentiation involved in phenotypic switching","termid":"GO:1905915"},{"relation_name":"positively_regulates","term_name":"cell differentiation involved in phenotypic switching","termid":"GO:0090679"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cell differentiation involved in phenotypic switching","synonyms":[{"name":"activation of cell differentiation involved in phenotypic switching","type":"narrow"},{"name":"up regulation of cell differentiation involved in phenotypic switching","type":"exact"},{"name":"up-regulation of cell differentiation involved in phenotypic switching","type":"exact"},{"name":"upregulation of cell differentiation involved in phenotypic switching","type":"exact"}],"termid":"GO:1905917"}


id: PBO:0026750
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_response_to_nitrogen_starvation","termid":"PBO:0026750"}


id: PBO:0060767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 11","termid":"PBO:0060767"}


id: GO:0102350
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: hexacosanoyl-CoA(4-) + NADP(3-) = trans-2-hexacosenoyl-CoA + NADPH + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete trans-cerot-2-enoyl-CoA reductase activity (obsolete GO:0102350)","termid":"GO:0102350"}


id: PBO:0057602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 939","termid":"PBO:0057602"}


id: PBO:0056640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 15","termid":"PBO:0056640"}


id: MOD:00673
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to a methylated asparagine, such as N4-methyl-L-asparagine, or N4,N4-dimethyl-L-asparagine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-asparagine residue","termid":"MOD:00903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"methylated asparagine","synonyms":[{"name":"MeAsn","type":"exact"}],"termid":"MOD:00673"}


id: PR:Q9Y7L2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC2A9.10 gene.","definition_xrefs":["UniProtKB:Q9Y7L2","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":"RNA methyltransferase C2A9.10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2A9.10","synonyms":[{"name":"Spom972h-SPBC2A9.10","type":"exact"}],"termid":"PR:Q9Y7L2"}


id: MONDO:0019476
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary cutaneous T-cell lymphoma","termid":"MONDO:0015758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0005093"],"is_obsolete":false,"name":"primary cutaneous peripheral T-cell lymphoma not otherwise specified","secondary_identifiers":["GARD:19078","ICD10CM:C84.4","MESH:D016411","MEDGEN:38240","MedDRA:10034623","Orphanet:86885","UMLS:C0079774"],"synonyms":[{"name":"primary cutaneous unspecified peripheral T-cell lymphoma","type":"exact"}],"termid":"MONDO:0019476","xrefs":{"Monarch":{"xref_id":"0019476"}}}


id: GO:0004920
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-10 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:signaling","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"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:0003674","GO:0038023"],"is_obsolete":false,"name":"interleukin-10 receptor activity","synonyms":[{"name":"IL-10 receptor activity","type":"exact"},{"name":"IL-10R","type":"exact"}],"termid":"GO:0004920"}


id: GO:2000602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of interphase of mitotic cell cycle.","definition_xrefs":["GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of interphase of mitotic cell cycle (obsolete GO:2000602)","synonyms":[{"name":"regulation of interphase of mitotic cell cycle","type":"exact"}],"termid":"GO:2000602"}


id: PBO:0031556
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_catalytic_activity","termid":"PBO:0031556"}


id: GO:0120154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ERBB4 signaling pathway.","definition_xrefs":["PMID:15219672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of ERBB signaling pathway","termid":"GO:1901185"},{"relation_name":"negatively_regulates","term_name":"ERBB4 signaling pathway","termid":"GO:0038130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of ERBB4 signaling pathway","termid":"GO:0120154"}


id: CHEBI:52646
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"A leptomycin having a (2E,10E,12E,16Z,18E)-double bond configuration as well as an ethyl substituent at position 17.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leptomycin B","termid":"CHEBI:52646"}


id: GO:0150165
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process mediated by a microRNA (miRNA) that stops, prevents or reduces the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:aruk"],"gene_count":0,"genotype_count":0,"name":"obsolete miRNA-mediated inhibition of transcription by RNA polymerase II (obsolete GO:0150165)","termid":"GO:0150165"}


id: PBO:0066957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 259","termid":"PBO:0066957"}


id: PBO:0073912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 16 member 3","termid":"PBO:0073912"}


id: PBO:0083686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Enolase, a phosphopyruvate hydratase; catalyzes the conversion of 2-phosphoglycerate to phosphoenolpyruvate; complements the growth defect of an ENO1 ENO2 double mutant in glucose","termid":"PBO:0083686"}


id: PBO:0061271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADPH oxidase 3","termid":"PBO:0061271"}


id: GO:1903425
data:
  {"annotated_genes":["SJAG_01973"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100312,113183],"is_not":false,"summary":null,"term":"GO:1903425"}]},"cv_name":"molecular_function","definition":"Enables the transfer of fluoride from one side of a membrane to the other.","definition_xrefs":["GO_REF:0000070","GOC:TermGenie","PMID:24173035"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic anion transmembrane transporter activity","termid":"GO:0008509"},{"relation_name":"is_a","term_name":"inorganic anion transmembrane transporter activity","termid":"GO:0015103"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01973":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"fluoride transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1903425","terms_by_termid":{"GO:1903425":null}}


id: MONDO:0034980
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A rare ophthalmic disorder characterized by an abnormally large optic disk (greater than 2.1 mm in diameter). The anomaly is usually bilateral with otherwise normal configuration of the disk, and typically associated with an increased cup-to-disc ratio, a round or horizontal oval optic cup, and an intact, pale-appearing neuroretinal rim. In a less frequent variant, a unilateral, anomalous superior excavation obliterates part of the adjacent neuroretinal rim. In general, visual acuity and visual fields are normal, except for an enlarged blind spot. Ciliary arteries are more common in megalopapilla.","definition_xrefs":["Orphanet:519402"],"gene_count":0,"genotype_count":0,"name":"obsolete isolated megalopapilla (obsolete MONDO:0034980)","secondary_identifiers":["icd11.foundation:1410300100","ICD10CM:Q14.2"],"termid":"MONDO:0034980","xrefs":{"Monarch":{"xref_id":"0034980"}}}


id: GO:0048519
data:
  {"annotated_genes":["SJAG_01157","SJAG_00410","SJAG_00142","SJAG_04056","SJAG_02409","SJAG_03898","SJAG_01053","SJAG_04061","SJAG_01401","SJAG_01778","SJAG_00786","SJAG_03383","SJAG_00460","SJAG_00875","SJAG_04186","SJAG_04332","SJAG_01429","SJAG_00640","SJAG_00987","SJAG_00391","SJAG_03876","SJAG_04551","SJAG_01754","SJAG_02858","SJAG_02778","SJAG_01878","SJAG_01297","SJAG_01745","SJAG_01373","SJAG_02231","SJAG_01436","SJAG_00304","SJAG_02374","SJAG_01521","SJAG_02392","SJAG_03664","SJAG_03130","SJAG_01511","SJAG_03097","SJAG_03997","SJAG_01837","SJAG_03635","SJAG_03680","SJAG_04597","SJAG_02336","SJAG_01677","SJAG_00279","SJAG_00975","SJAG_00963","SJAG_03081","SJAG_03927","SJAG_01515","SJAG_03185","SJAG_01708","SJAG_01601","SJAG_02700","SJAG_03893","SJAG_00990","SJAG_03689","SJAG_02380","SJAG_01825","SJAG_04601","SJAG_01176","SJAG_02622","SJAG_02795","SJAG_04500","SJAG_00701","SJAG_02594","SJAG_04813","SJAG_01728","SJAG_00290","SJAG_03067","SJAG_04206","SJAG_04203","SJAG_01528","SJAG_00266","SJAG_02169","SJAG_01199","SJAG_03850","SJAG_02098","SJAG_03089","SJAG_00676","SJAG_02255","SJAG_01830","SJAG_04030","SJAG_03681","SJAG_02311","SJAG_05240","SJAG_02342","SJAG_04084","SJAG_01376","SJAG_00623","SJAG_00425","SJAG_01205","SJAG_04153","SJAG_01330","SJAG_03170","SJAG_02239","SJAG_01068","SJAG_05276","SJAG_03696","SJAG_00364","SJAG_04268","SJAG_01919","SJAG_03501","SJAG_02370","SJAG_02638","SJAG_00797","SJAG_00600","SJAG_03132","SJAG_02382","SJAG_01823","SJAG_00071","SJAG_05313","SJAG_05314","SJAG_04682","SJAG_03263","SJAG_00610","SJAG_01082","SJAG_00685","SJAG_01000","SJAG_03160","SJAG_01529","SJAG_04584","SJAG_01412","SJAG_05322","SJAG_00759","SJAG_00327","SJAG_03353","SJAG_04879","SJAG_02573","SJAG_03529","SJAG_00293","SJAG_03072","SJAG_01540","SJAG_02725","SJAG_03952","SJAG_02074","SJAG_01843","SJAG_00160","SJAG_02119","SJAG_02808","SJAG_04118","SJAG_01956","SJAG_04259","SJAG_04512","SJAG_03627","SJAG_04396","SJAG_00457","SJAG_04755","SJAG_00341","SJAG_04638","SJAG_03970","SJAG_03319","SJAG_01191","SJAG_04360","SJAG_00082","SJAG_00229","SJAG_03113","SJAG_02990","SJAG_01245","SJAG_03799","SJAG_05978","SJAG_00429","SJAG_00472","SJAG_04025","SJAG_04943","SJAG_01599","SJAG_02908","SJAG_01926","SJAG_02592","SJAG_02724","SJAG_00058","SJAG_03916","SJAG_01114","SJAG_00855","SJAG_05694","SJAG_03048","SJAG_04671","SJAG_02013","SJAG_00926","SJAG_04369","SJAG_04462","SJAG_03942","SJAG_03047","SJAG_04455","SJAG_01230","SJAG_03845","SJAG_02426","SJAG_04607","SJAG_02773","SJAG_02898","SJAG_03454","SJAG_02379","SJAG_00456","SJAG_03745","SJAG_00335","SJAG_03984","SJAG_04126","SJAG_03283","SJAG_04198","SJAG_03356","SJAG_01464","SJAG_00581","SJAG_02720","SJAG_01625","SJAG_03276","SJAG_03234","SJAG_00285","SJAG_03438","SJAG_04699","SJAG_01605","SJAG_04825","SJAG_02698","SJAG_04287","SJAG_02266","SJAG_02036","SJAG_02921","SJAG_00441","SJAG_01836","SJAG_03597","SJAG_03805","SJAG_00845","SJAG_00163","SJAG_01254","SJAG_02381","SJAG_01076","SJAG_03042","SJAG_04824","SJAG_00934","SJAG_00087","SJAG_00423","SJAG_04586","SJAG_03631","SJAG_03624","SJAG_03602","SJAG_03371","SJAG_01680","SJAG_01311","SJAG_06270","SJAG_02404","SJAG_02621","SJAG_02981","SJAG_05373","SJAG_00961","SJAG_06592","SJAG_01331","SJAG_03883","SJAG_00969","SJAG_02879","SJAG_03945","SJAG_02576","SJAG_04039","SJAG_01187","SJAG_02005","SJAG_16457","SJAG_03070","SJAG_02383","SJAG_03394","SJAG_04350","SJAG_00302","SJAG_03157","SJAG_01938","SJAG_02233","SJAG_00823","SJAG_04312","SJAG_04768","SJAG_01699","SJAG_00247","SJAG_00209","SJAG_03543","SJAG_01804","SJAG_05000","SJAG_00966","SJAG_01944","SJAG_00686","SJAG_02104","SJAG_04884","SJAG_03591","SJAG_01867","SJAG_04141","SJAG_02165","SJAG_03706","SJAG_02701","SJAG_04280","SJAG_00053","SJAG_02332","SJAG_03592","SJAG_01044","SJAG_05346","SJAG_01822","SJAG_00156","SJAG_01873","SJAG_01118","SJAG_00896","SJAG_02846","SJAG_01675","SJAG_01579","SJAG_03678","SJAG_00169","SJAG_02752","SJAG_04291","SJAG_04283","SJAG_04818","SJAG_01983","SJAG_04006","SJAG_00526","SJAG_03118","SJAG_02730","SJAG_01008","SJAG_01010","SJAG_01184","SJAG_04921","SJAG_04394","SJAG_01818","SJAG_05243","SJAG_01253","SJAG_03179","SJAG_02817","SJAG_00769","SJAG_00642","SJAG_01993","SJAG_02385","SJAG_01210","SJAG_04880","SJAG_01942","SJAG_00452","SJAG_01936","SJAG_04213","SJAG_01046","SJAG_03869","SJAG_00991","SJAG_01679","SJAG_02451","SJAG_04321","SJAG_01084","SJAG_01252","SJAG_00824","SJAG_00573","SJAG_00507","SJAG_04427","SJAG_04855","SJAG_00318","SJAG_02416","SJAG_04253","SJAG_03023","SJAG_00756","SJAG_00486","SJAG_01386","SJAG_00289","SJAG_04381","SJAG_04946","SJAG_00145","SJAG_02275","SJAG_01906","SJAG_04527","SJAG_00414","SJAG_00670","SJAG_00883","SJAG_03982","SJAG_04249","SJAG_03886","SJAG_00343","SJAG_04574","SJAG_03455","SJAG_02601","SJAG_02000","SJAG_01790","SJAG_01075","SJAG_02540","SJAG_01707","SJAG_01855","SJAG_01218","SJAG_03486","SJAG_01431","SJAG_02444","SJAG_00802","SJAG_03448","SJAG_03695","SJAG_05010","SJAG_04407","SJAG_01610","SJAG_01799","SJAG_00052","SJAG_04942","SJAG_03128","SJAG_03720","SJAG_04522","SJAG_01716","SJAG_03844","SJAG_00424","SJAG_03473","SJAG_03126","SJAG_04999","SJAG_02213","SJAG_04389","SJAG_04640","SJAG_03327","SJAG_00369","SJAG_02514","SJAG_00124","SJAG_00475","SJAG_01894","SJAG_00690","SJAG_02401","SJAG_03026","SJAG_02771","SJAG_02723","SJAG_04613","SJAG_02244","SJAG_00854","SJAG_03466","SJAG_03143","SJAG_03223","SJAG_02563","SJAG_00226","SJAG_00792","SJAG_03073","SJAG_03940","SJAG_01146","SJAG_03193","SJAG_05288","SJAG_05014","SJAG_03854","SJAG_00296","SJAG_01910","SJAG_00861","SJAG_04026","SJAG_02765","SJAG_02026","SJAG_01142","SJAG_03355","SJAG_02481","SJAG_03581","SJAG_04140","SJAG_03508","SJAG_00996","SJAG_02162","SJAG_04910","SJAG_04539"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117749],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:0061158"},{"annotations":[99585,117750,78288,89704],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0070935"},{"annotations":[98399,113761,87772,91834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"},{"annotations":[108504,89856,94657],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051728"},{"annotations":[99060,115426,109936,117526,98622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033562"},{"annotations":[113045,110720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140719"},{"annotations":[103377,106701,113221,99088,107713,113711,115344,90237,111409],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[105604,111452,109394,91061,109345,112918],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000290"},{"annotations":[105046,92057],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031087"},{"annotations":[108772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000077"},{"annotations":[93583,102707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140718"},{"annotations":[98625,112057,101499,102708,101498,116567,114697,117193,98651,87671,90268,102540,95662,98406,112056,112500,112055,101500,93584],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033696"},{"annotations":[92111,101502,103574,118606,94113,112060,117148,91298,93856,103672,111654,118607,103673,101503,90780,101501,112059,114852,113428,108926,113562,90269,101897,114449,109407,112058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031507"},{"annotations":[91752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071044"},{"annotations":[113941,105785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[92034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044778"},{"annotations":[106081,90940,115503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[115504,88573,106082,113701],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051598"},{"annotations":[101287,105786,116112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033316"},{"annotations":[100027,115448,100925,89505,93914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044878"},{"annotations":[106083,108773,115449,113702,110650,117151,93066,113912,77532,93444,115678,79553,98690,91301,101847],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044773"},{"annotations":[93466,98691,107301,88632,116246,92035,90941,108774,115505,116547,106084,116716,98857,111484,100028,93445,102805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033314"},{"annotations":[115346,88458,108346,101848,101111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031568"},{"annotations":[90817,109132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[94045,97934,115450,95354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031569"},{"annotations":[108775,98859,116461,89724,113703,111180,88633,91302,88062,93446,100543,90942,100029,117152,106085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007095"},{"annotations":[88634,88063,90943,106086,100348,107131,111485,92036,101013,98692,98860,116548,115507,88679,101849,111181,95515,115506,94046,89959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031573"},{"annotations":[101288,116115,98932,113944,90239,109369,113225,114999,105787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[117354,114296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006402"},{"annotations":[117547],"is_not":false,"rel_names":["regulates","is_a","positively_regulates"],"summary":null,"term":"GO:0061157"},{"annotations":[88997,95755],"is_not":false,"rel_names":["negatively_regulates","regulates","is_a"],"summary":null,"term":"GO:0048255"},{"annotations":[103860,89923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[115825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106072"},{"annotations":[92254,99932,91596,107434,115826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110034"},{"annotations":[101850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905785"},{"annotations":[107435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060195"},{"annotations":[90387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034316"},{"annotations":[110651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[101851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902424"},{"annotations":[117800,108723],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010507"},{"annotations":[90240],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051517"},{"annotations":[100487,115573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106057"},{"annotations":[112802,90727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905949"},{"annotations":[101852,106115,103926,105438,108724,117801,105280],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:0110045"},{"annotations":[106512,95355,103288,98939,107076,117751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903138"},{"annotations":[98082,98794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0022408"},{"annotations":[116007,101853,91597,92717,87719,101112,88325,95890,104381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031138"},{"annotations":[94658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140538"},{"annotations":[97783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000432"},{"annotations":[117664,95093,98940,114297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000766"},{"annotations":[90818,109133,111602],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904689"},{"annotations":[93873,98834,92318,109134,92022,115059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"},{"annotations":[99166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010974"},{"annotations":[100564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045892"},{"annotations":[101854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001033"},{"annotations":[94085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045806"},{"annotations":[99364,96041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904293"},{"annotations":[93383],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"},{"annotations":[111210],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904332"},{"annotations":[90473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904846"},{"annotations":[101855,92346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001100"},{"annotations":[110714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045717"},{"annotations":[93564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905569"},{"annotations":[105721,103040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060257"},{"annotations":[117527,99061,115427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070317"},{"annotations":[91668,92831,108347,91248,88459,98377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000134"},{"annotations":[111923,111014,110886,113704,108032,103982,113913,92430,95356,89506,115451,106116,100488,92718,106479,111271,93874,93067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010972"},{"annotations":[111015,115452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110031"},{"annotations":[100401,88326,115428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010629"},{"annotations":[96722,92705,92741,102602,113588,96834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045814"},{"annotations":[101632,102330,88949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902660"},{"annotations":[78413,90445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045719"},{"annotations":[75583,72605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"},{"annotations":[87604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042997"},{"annotations":[106117,93875,90919,103983,100030,92431,87720,101339,106312,105375,93735,105281,105963,114975,115515,113914,108472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010515"},{"annotations":[110824,114923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"},{"annotations":[117385],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905560"},{"annotations":[87605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905533"},{"annotations":[106118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016242"},{"annotations":[87721,106603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043409"},{"annotations":[110652,115827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051447"},{"annotations":[98198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902103"},{"annotations":[115750],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090258"},{"annotations":[101535,105921],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010637"},{"annotations":[101856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903500"},{"annotations":[103184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903472"},{"annotations":[108348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045930"},{"annotations":[116293,108349],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903464"},{"annotations":[101633,92347,99167,101857,106563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902413"},{"annotations":[97271,101858,108350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903467"},{"annotations":[105788,115000],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045841"},{"annotations":[102763],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000816"},{"annotations":[93706],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[101859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902845"},{"annotations":[101860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904537"},{"annotations":[88998],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:1902373"},{"annotations":[89298],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:0120271"},{"annotations":[91178],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:0060212"},{"annotations":[116522,117752,91171,98941,94537,95475],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903753"},{"annotations":[106604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180040"},{"annotations":[92826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090029"},{"annotations":[112188,109190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071072"},{"annotations":[100931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062168"},{"annotations":[101861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905757"},{"annotations":[106416,89914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032435"},{"annotations":[105282],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042308"},{"annotations":[95357,90474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903067"},{"annotations":[93915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140325"},{"annotations":[106702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902543"},{"annotations":[113915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900181"},{"annotations":[95358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903077"},{"annotations":[110816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046580"},{"annotations":[106119],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:0061188"},{"annotations":[107436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045128"},{"annotations":[107951],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0060906"},{"annotations":[104813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035024"},{"annotations":[105776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902369"},{"annotations":[106703,95143,91240,115347,109627,92348,104507,99168,90241,100766,92961,99090,107006,92432,106564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031030"},{"annotations":[114782,105727,106046,91249,106871,105824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045875"},{"annotations":[111163,90748,105365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000639"},{"annotations":[90771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032007"},{"annotations":[110408,102496,100941,106617,109135,114022,113418,93679,87537,115929,116486,92832,99072,112601,98378,106864,108725,117665,95602,104601,115574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904262"},{"annotations":[115720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903940"},{"annotations":[105964,110595,103041,112418,95786,106196,106214,93384,100489,116812,93565,98388,105283,89560,102266,93280,103743,100467,90765,107693,108033,108473,113705,114023,115077,105376,93242,92798,94230,93736,106467,110174,105722,105975,111541,90693,91669,94147,107919,103441,107437,88358,115516,79966,104498,87110,92896,91645,101340,113272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000122"},{"annotations":[95893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016480"},{"annotations":[100490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010621"},{"annotations":[117372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034244"},{"annotations":[98942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001125"},{"annotations":[87606],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905530"},{"annotations":[100942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061192"},{"annotations":[94461,88959,101569,105933,104730,100529,103885,95418,96036,92579,114887,115328,117736,88596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071028"},{"annotations":[117549,90380,90305,91371,96230,91754,110753,98595,108715,87013,106921,103784,108696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033621"},{"annotations":[92946,96748,112705,106922,117550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071031"},{"annotations":[115776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071032"},{"annotations":[88354,90306,91875,94504,108716,109247,114992,105777,87014,117551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071030"},{"annotations":[104731,91757,101570,105934,96749,103886,114888,117737,106923,95419,115329,92580],"is_not":false,"rel_names":["positively_regulates","is_a","regulates"],"summary":null,"term":"GO:0071042"},{"annotations":[94462,104382,95127,107999,91206,101658,109347,114772,102010,115853,110703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000956"},{"annotations":[92582,96752,115331,116669,100729,104733,95421,101572,105936,106926,88271,91032,103888,89310,108284,115594,117739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070478"},{"annotations":[99423,97641,97555,89209,110521,114589,112767],"is_not":false,"rel_names":["positively_regulates","is_a","regulates"],"summary":null,"term":"GO:0000288"},{"annotations":[113550,115475,106644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070966"},{"annotations":[105937,115476,115595,96753,106927,117740,108285,115332,103889,101573,104734,95422,116670,92583,100730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070481"},{"annotations":[105360,89311,104235,114821,89415,91033,113022,89824,99272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000184"},{"annotations":[96000,104251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000294"},{"annotations":[93841,91441,98016,89299,90295,91501,116048,116609,108662,92103,95011,92008,115101,92910,102515],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000289"},{"annotations":[102710,97760,98631,101508,111556,111655,112737,113431,93586,113861,112066,90781,107623,103575,96231,101507,101509,110723,89725,102267,109938,92332,112064,89561,91581,92947,112065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031508"},{"annotations":[90856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140462"},{"annotations":[91179],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036450"},{"annotations":[90296,95128,116671],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:1990074"},{"annotations":[115930,117667],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0140648"},{"annotations":[98466],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0031453"},{"annotations":[113226],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[116119],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[106123],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0120272"},{"annotations":[89210,100499,104384],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0060213"},{"annotations":[90694],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090053"},{"annotations":[90695,93879,109800],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090055"},{"annotations":[118604,118605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016441"},{"annotations":[117417,117529,87891,107246],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990431"},{"annotations":[113862,89562,91582,103576,107624,111557,112738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000183"},{"annotations":[94049,101876,104385,108506,101114],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0110044"},{"annotations":[98073,90325],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0031445"},{"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":[116071],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0061013"},{"annotations":[87922,116727],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0043488"},{"annotations":[89707,91034,89312],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000815"},{"annotations":[98017],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0060211"},{"annotations":[96691,99795],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090052"},{"annotations":[117194],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010964"},{"annotations":[102711],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902681"},{"annotations":[117554,99796,91372,96692,117195],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902801"},{"annotations":[91373,92333,117555],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043628"},{"annotations":[87015,106016,111308,117556,89300,91762,115102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031047"},{"annotations":[106820,112502,117530,103577,99062,107247,114013,113111,108577,117418,111309],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031048"},{"annotations":[108127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061454"},{"annotations":[106100,101766,107976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043111"},{"annotations":[98861,107977,102712,106101],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0011000"},{"annotations":[98862,101767,114465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031582"},{"annotations":[98863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090001"},{"annotations":[101768],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071807"},{"annotations":[98948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141014"},{"annotations":[93587,110724,92258,103578,98632,117531,107440,110661,95024,111558,96232,99064,90782,113432,115430,111656,117138,113112,112739,103674,107625,109939,91583,102713,118250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030466"},{"annotations":[107248,117532],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990432"},{"annotations":[108578,99065],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030422"},{"annotations":[87016,115982,90308,109940,103675,111559,117557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902794"},{"annotations":[105778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902795"},{"annotations":[113433],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141194"},{"annotations":[88349,88294,96233,110106,115431,113748,110662,109941,90783,114867,118251,117419,94840,113113,111657,114014,117139,98633,106017,93599,117533,99066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140727"},{"annotations":[98634,103579,109942,110725,91584,107626,113114,93588,112740,90784,102714,111560,103676,113434,96234,117140,87944,89726,89564,97761,117534,118252],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031509"},{"annotations":[90151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090669"},{"annotations":[115984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141005"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a biological process. Biological processes are regulated by many means; examples include the control of gene expression, protein modification or interaction with a protein or substrate molecule.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process","termid":"GO:0050789"},{"relation_name":"negatively_regulates","term_name":"biological_process","termid":"GO:0008150"}],"gene_count":440,"genes_by_uniquename":{"SJAG_00052":null,"SJAG_00053":null,"SJAG_00058":null,"SJAG_00071":null,"SJAG_00082":null,"SJAG_00087":null,"SJAG_00124":null,"SJAG_00142":null,"SJAG_00145":null,"SJAG_00156":null,"SJAG_00160":null,"SJAG_00163":null,"SJAG_00169":null,"SJAG_00209":null,"SJAG_00226":null,"SJAG_00229":null,"SJAG_00247":null,"SJAG_00266":null,"SJAG_00279":null,"SJAG_00285":null,"SJAG_00289":null,"SJAG_00290":null,"SJAG_00293":null,"SJAG_00296":null,"SJAG_00302":null,"SJAG_00304":null,"SJAG_00318":null,"SJAG_00327":null,"SJAG_00335":null,"SJAG_00341":null,"SJAG_00343":null,"SJAG_00364":null,"SJAG_00369":null,"SJAG_00391":null,"SJAG_00410":null,"SJAG_00414":null,"SJAG_00423":null,"SJAG_00424":null,"SJAG_00425":null,"SJAG_00429":null,"SJAG_00441":null,"SJAG_00452":null,"SJAG_00456":null,"SJAG_00457":null,"SJAG_00460":null,"SJAG_00472":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00507":null,"SJAG_00526":null,"SJAG_00573":null,"SJAG_00581":null,"SJAG_00600":null,"SJAG_00610":null,"SJAG_00623":null,"SJAG_00640":null,"SJAG_00642":null,"SJAG_00670":null,"SJAG_00676":null,"SJAG_00685":null,"SJAG_00686":null,"SJAG_00690":null,"SJAG_00701":null,"SJAG_00756":null,"SJAG_00759":null,"SJAG_00769":null,"SJAG_00786":null,"SJAG_00792":null,"SJAG_00797":null,"SJAG_00802":null,"SJAG_00823":null,"SJAG_00824":null,"SJAG_00845":null,"SJAG_00854":null,"SJAG_00855":null,"SJAG_00861":null,"SJAG_00875":null,"SJAG_00883":null,"SJAG_00896":null,"SJAG_00926":null,"SJAG_00934":null,"SJAG_00961":null,"SJAG_00963":null,"SJAG_00966":null,"SJAG_00969":null,"SJAG_00975":null,"SJAG_00987":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_00996":null,"SJAG_01000":null,"SJAG_01008":null,"SJAG_01010":null,"SJAG_01044":null,"SJAG_01046":null,"SJAG_01053":null,"SJAG_01068":null,"SJAG_01075":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01114":null,"SJAG_01118":null,"SJAG_01142":null,"SJAG_01146":null,"SJAG_01157":null,"SJAG_01176":null,"SJAG_01184":null,"SJAG_01187":null,"SJAG_01191":null,"SJAG_01199":null,"SJAG_01205":null,"SJAG_01210":null,"SJAG_01218":null,"SJAG_01230":null,"SJAG_01245":null,"SJAG_01252":null,"SJAG_01253":null,"SJAG_01254":null,"SJAG_01297":null,"SJAG_01311":null,"SJAG_01330":null,"SJAG_01331":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01386":null,"SJAG_01401":null,"SJAG_01412":null,"SJAG_01429":null,"SJAG_01431":null,"SJAG_01436":null,"SJAG_01464":null,"SJAG_01511":null,"SJAG_01515":null,"SJAG_01521":null,"SJAG_01528":null,"SJAG_01529":null,"SJAG_01540":null,"SJAG_01579":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01605":null,"SJAG_01610":null,"SJAG_01625":null,"SJAG_01675":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01699":null,"SJAG_01707":null,"SJAG_01708":null,"SJAG_01716":null,"SJAG_01728":null,"SJAG_01745":null,"SJAG_01754":null,"SJAG_01778":null,"SJAG_01790":null,"SJAG_01799":null,"SJAG_01804":null,"SJAG_01818":null,"SJAG_01822":null,"SJAG_01823":null,"SJAG_01825":null,"SJAG_01830":null,"SJAG_01836":null,"SJAG_01837":null,"SJAG_01843":null,"SJAG_01855":null,"SJAG_01867":null,"SJAG_01873":null,"SJAG_01878":null,"SJAG_01894":null,"SJAG_01906":null,"SJAG_01910":null,"SJAG_01919":null,"SJAG_01926":null,"SJAG_01936":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01944":null,"SJAG_01956":null,"SJAG_01983":null,"SJAG_01993":null,"SJAG_02000":null,"SJAG_02005":null,"SJAG_02013":null,"SJAG_02026":null,"SJAG_02036":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02119":null,"SJAG_02162":null,"SJAG_02165":null,"SJAG_02169":null,"SJAG_02213":null,"SJAG_02231":null,"SJAG_02233":null,"SJAG_02239":null,"SJAG_02244":null,"SJAG_02255":null,"SJAG_02266":null,"SJAG_02275":null,"SJAG_02311":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02381":null,"SJAG_02382":null,"SJAG_02383":null,"SJAG_02385":null,"SJAG_02392":null,"SJAG_02401":null,"SJAG_02404":null,"SJAG_02409":null,"SJAG_02416":null,"SJAG_02426":null,"SJAG_02444":null,"SJAG_02451":null,"SJAG_02481":null,"SJAG_02514":null,"SJAG_02540":null,"SJAG_02563":null,"SJAG_02573":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02594":null,"SJAG_02601":null,"SJAG_02621":null,"SJAG_02622":null,"SJAG_02638":null,"SJAG_02698":null,"SJAG_02700":null,"SJAG_02701":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02724":null,"SJAG_02725":null,"SJAG_02730":null,"SJAG_02752":null,"SJAG_02765":null,"SJAG_02771":null,"SJAG_02773":null,"SJAG_02778":null,"SJAG_02795":null,"SJAG_02808":null,"SJAG_02817":null,"SJAG_02846":null,"SJAG_02858":null,"SJAG_02879":null,"SJAG_02898":null,"SJAG_02908":null,"SJAG_02921":null,"SJAG_02981":null,"SJAG_02990":null,"SJAG_03023":null,"SJAG_03026":null,"SJAG_03042":null,"SJAG_03047":null,"SJAG_03048":null,"SJAG_03067":null,"SJAG_03070":null,"SJAG_03072":null,"SJAG_03073":null,"SJAG_03081":null,"SJAG_03089":null,"SJAG_03097":null,"SJAG_03113":null,"SJAG_03118":null,"SJAG_03126":null,"SJAG_03128":null,"SJAG_03130":null,"SJAG_03132":null,"SJAG_03143":null,"SJAG_03157":null,"SJAG_03160":null,"SJAG_03170":null,"SJAG_03179":null,"SJAG_03185":null,"SJAG_03193":null,"SJAG_03223":null,"SJAG_03234":null,"SJAG_03263":null,"SJAG_03276":null,"SJAG_03283":null,"SJAG_03319":null,"SJAG_03327":null,"SJAG_03353":null,"SJAG_03355":null,"SJAG_03356":null,"SJAG_03371":null,"SJAG_03383":null,"SJAG_03394":null,"SJAG_03438":null,"SJAG_03448":null,"SJAG_03454":null,"SJAG_03455":null,"SJAG_03466":null,"SJAG_03473":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03508":null,"SJAG_03529":null,"SJAG_03543":null,"SJAG_03581":null,"SJAG_03591":null,"SJAG_03592":null,"SJAG_03597":null,"SJAG_03602":null,"SJAG_03624":null,"SJAG_03627":null,"SJAG_03631":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03678":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03689":null,"SJAG_03695":null,"SJAG_03696":null,"SJAG_03706":null,"SJAG_03720":null,"SJAG_03745":null,"SJAG_03799":null,"SJAG_03805":null,"SJAG_03844":null,"SJAG_03845":null,"SJAG_03850":null,"SJAG_03854":null,"SJAG_03869":null,"SJAG_03876":null,"SJAG_03883":null,"SJAG_03886":null,"SJAG_03893":null,"SJAG_03898":null,"SJAG_03916":null,"SJAG_03927":null,"SJAG_03940":null,"SJAG_03942":null,"SJAG_03945":null,"SJAG_03952":null,"SJAG_03970":null,"SJAG_03982":null,"SJAG_03984":null,"SJAG_03997":null,"SJAG_04006":null,"SJAG_04025":null,"SJAG_04026":null,"SJAG_04030":null,"SJAG_04039":null,"SJAG_04056":null,"SJAG_04061":null,"SJAG_04084":null,"SJAG_04118":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04141":null,"SJAG_04153":null,"SJAG_04186":null,"SJAG_04198":null,"SJAG_04203":null,"SJAG_04206":null,"SJAG_04213":null,"SJAG_04249":null,"SJAG_04253":null,"SJAG_04259":null,"SJAG_04268":null,"SJAG_04280":null,"SJAG_04283":null,"SJAG_04287":null,"SJAG_04291":null,"SJAG_04312":null,"SJAG_04321":null,"SJAG_04332":null,"SJAG_04350":null,"SJAG_04360":null,"SJAG_04369":null,"SJAG_04381":null,"SJAG_04389":null,"SJAG_04394":null,"SJAG_04396":null,"SJAG_04407":null,"SJAG_04427":null,"SJAG_04455":null,"SJAG_04462":null,"SJAG_04500":null,"SJAG_04512":null,"SJAG_04522":null,"SJAG_04527":null,"SJAG_04539":null,"SJAG_04551":null,"SJAG_04574":null,"SJAG_04584":null,"SJAG_04586":null,"SJAG_04597":null,"SJAG_04601":null,"SJAG_04607":null,"SJAG_04613":null,"SJAG_04638":null,"SJAG_04640":null,"SJAG_04671":null,"SJAG_04682":null,"SJAG_04699":null,"SJAG_04755":null,"SJAG_04768":null,"SJAG_04813":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_04825":null,"SJAG_04855":null,"SJAG_04879":null,"SJAG_04880":null,"SJAG_04884":null,"SJAG_04910":null,"SJAG_04921":null,"SJAG_04942":null,"SJAG_04943":null,"SJAG_04946":null,"SJAG_04999":null,"SJAG_05000":null,"SJAG_05010":null,"SJAG_05014":null,"SJAG_05240":null,"SJAG_05243":null,"SJAG_05276":null,"SJAG_05288":null,"SJAG_05313":null,"SJAG_05314":null,"SJAG_05322":null,"SJAG_05346":null,"SJAG_05373":null,"SJAG_05694":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_06592":null,"SJAG_16457":null},"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 biological process","references_by_uniquename":{"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"PMID:35226668":null},"secondary_identifiers":["GO:0043118"],"synonyms":[{"name":"down regulation of biological process","type":"exact"},{"name":"down-regulation of biological process","type":"exact"},{"name":"downregulation of biological process","type":"exact"},{"name":"inhibition of biological process","type":"narrow"},{"name":"negative regulation of physiological process","type":"exact"}],"termid":"GO:0048519","terms_by_termid":{"GO:0000077":null,"GO:0000122":null,"GO:0000183":null,"GO:0000184":null,"GO:0000288":null,"GO:0000289":null,"GO:0000290":null,"GO:0000294":null,"GO:0000956":null,"GO:0001100":null,"GO:0006402":null,"GO:0007094":null,"GO:0007095":null,"GO:0010507":null,"GO:0010515":null,"GO:0010621":null,"GO:0010629":null,"GO:0010637":null,"GO:0010895":null,"GO:0010964":null,"GO:0010972":null,"GO:0010974":null,"GO:0011000":null,"GO:0016242":null,"GO:0016441":null,"GO:0016480":null,"GO:0022408":null,"GO:0030422":null,"GO:0030466":null,"GO:0031030":null,"GO:0031047":null,"GO:0031048":null,"GO:0031087":null,"GO:0031138":null,"GO:0031445":null,"GO:0031453":null,"GO:0031507":null,"GO:0031508":null,"GO:0031509":null,"GO:0031568":null,"GO:0031569":null,"GO:0031571":null,"GO:0031573":null,"GO:0031582":null,"GO:0032007":null,"GO:0032435":null,"GO:0033314":null,"GO:0033315":null,"GO:0033316":null,"GO:0033562":null,"GO:0033621":null,"GO:0033696":null,"GO:0034244":null,"GO:0034316":null,"GO:0035024":null,"GO:0036450":null,"GO:0042308":null,"GO:0042997":null,"GO:0043111":null,"GO:0043409":null,"GO:0043488":null,"GO:0043628":null,"GO:0044773":null,"GO:0044778":null,"GO:0044878":null,"GO:0045128":null,"GO:0045717":null,"GO:0045719":null,"GO:0045806":null,"GO:0045814":null,"GO:0045820":null,"GO:0045841":null,"GO:0045875":null,"GO:0045892":null,"GO:0045930":null,"GO:0046580":null,"GO:0048255":null,"GO:0051016":null,"GO:0051447":null,"GO:0051517":null,"GO:0051598":null,"GO:0051728":null,"GO:0060195":null,"GO:0060211":null,"GO:0060212":null,"GO:0060213":null,"GO:0060257":null,"GO:0060906":null,"GO:0061013":null,"GO:0061157":null,"GO:0061158":null,"GO:0061188":null,"GO:0061192":null,"GO:0061454":null,"GO:0062168":null,"GO:0070317":null,"GO:0070478":null,"GO:0070481":null,"GO:0070935":null,"GO:0070966":null,"GO:0071028":null,"GO:0071030":null,"GO:0071031":null,"GO:0071032":null,"GO:0071042":null,"GO:0071044":null,"GO:0071072":null,"GO:0071807":null,"GO:0075297":null,"GO:0090001":null,"GO:0090029":null,"GO:0090052":null,"GO:0090053":null,"GO:0090055":null,"GO:0090258":null,"GO:0090266":null,"GO:0090267":null,"GO:0090669":null,"GO:0106057":null,"GO:0106072":null,"GO:0110031":null,"GO:0110034":null,"GO:0110044":null,"GO:0110045":null,"GO:0120271":null,"GO:0120272":null,"GO:0140325":null,"GO:0140462":null,"GO:0140499":null,"GO:0140538":null,"GO:0140648":null,"GO:0140718":null,"GO:0140719":null,"GO:0140727":null,"GO:0141005":null,"GO:0141014":null,"GO:0141194":null,"GO:0180040":null,"GO:1900181":null,"GO:1902103":null,"GO:1902369":null,"GO:1902373":null,"GO:1902413":null,"GO:1902424":null,"GO:1902426":null,"GO:1902543":null,"GO:1902647":null,"GO:1902660":null,"GO:1902681":null,"GO:1902794":null,"GO:1902795":null,"GO:1902801":null,"GO:1902845":null,"GO:1903067":null,"GO:1903077":null,"GO:1903138":null,"GO:1903464":null,"GO:1903467":null,"GO:1903472":null,"GO:1903500":null,"GO:1903753":null,"GO:1903940":null,"GO:1904262":null,"GO:1904293":null,"GO:1904332":null,"GO:1904537":null,"GO:1904689":null,"GO:1904846":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:1905530":null,"GO:1905533":null,"GO:1905560":null,"GO:1905569":null,"GO:1905757":null,"GO:1905785":null,"GO:1905949":null,"GO:1990074":null,"GO:1990431":null,"GO:1990432":null,"GO:1990625":null,"GO:2000134":null,"GO:2000432":null,"GO:2000639":null,"GO:2000766":null,"GO:2000815":null,"GO:2000816":null,"GO:2001033":null,"GO:2001125":null,"GO:2001211":null}}


id: MONDO:0100029
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An immune epilepsy where the underlying cause is antibody mediated.","direct_ancestors":[{"relation_name":"is_a","term_name":"immune epilepsy","termid":"MONDO:0100028"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"antibody mediated epilepsy","termid":"MONDO:0100029","xrefs":{"Monarch":{"xref_id":"0100029"}}}


id: PBO:0090332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial 2' O-ribose methyltransferase Mrm2","termid":"PBO:0090332"}


id: MONDO:1011811
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cancer or benign tumor, non-human animal","termid":"MONDO:1011305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital melanoma, non-human animal","secondary_identifiers":["OMIA:000634"],"termid":"MONDO:1011811","xrefs":{"Monarch":{"xref_id":"1011811"}}}


id: PBO:0089296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenine phosphoribosyltransferase (APRT) Apt1","termid":"PBO:0089296"}


id: MONDO:0005910
data:
  {"annotated_genes":["SJAG_04743"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010600"}]},"cv_name":"mondo","definition":"Disorders in which phagocytic cells cannot kill ingested bacteria; characterized by frequent recurring infection with formulation of granulomas.","definition_xrefs":["MESH:D010585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"},{"relation_name":"is_a","term_name":"leukocyte disorder","termid":"MONDO:0004805"},{"relation_name":"is_a","term_name":"phagocytic cell dysfunction","termid":"MONDO:0024627"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04743":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"phagocyte bactericidal dysfunction","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0007433","MEDGEN:14713","DOID:3262","UMLS:C0031306"],"synonyms":[{"name":"phagocytic dysfunction","type":"exact"}],"termid":"MONDO:0005910","terms_by_termid":{"MONDO:0010600":null},"xrefs":{"Monarch":{"xref_id":"0005910"}}}


id: GO:0060707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a trophoblast giant cell of the placenta. Trophoblast giant cells are the cell of the placenta that line the maternal decidua.","definition_xrefs":["PMID:16269175","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation involved in embryonic placenta development","termid":"GO:0060706"}],"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":"trophoblast giant cell differentiation","termid":"GO:0060707"}


id: PBO:0039361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APC membrane recruitment protein 3","termid":"PBO:0039361"}


id: GO:0015952
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways by which a purine deoxyribonucleotide is synthesized from another purine deoxyribonucleotide.","definition_xrefs":["GOC:mah","ISBN:0306444747","ISBN:0471394831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine deoxyribonucleotide metabolic process","termid":"GO:0009151"},{"relation_name":"is_a","term_name":"purine nucleotide interconversion","termid":"GO:0015950"}],"gene_count":0,"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:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"purine deoxyribonucleotide interconversion","termid":"GO:0015952"}


id: GO:0045753
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of acetate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"regulation of acetate catabolic process","termid":"GO:0045734"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"negatively_regulates","term_name":"acetate catabolic process","termid":"GO:0045733"}],"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"},{"rel_name":"negatively_regulates","termid":"GO:0044248"},{"rel_name":"regulates","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0044248","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"negative regulation of acetate catabolic process","synonyms":[{"name":"down regulation of acetate catabolic process","type":"exact"},{"name":"down-regulation of acetate catabolic process","type":"exact"},{"name":"downregulation of acetate catabolic process","type":"exact"},{"name":"inhibition of acetate catabolic process","type":"narrow"},{"name":"negative regulation of acetate breakdown","type":"exact"},{"name":"negative regulation of acetate catabolism","type":"exact"},{"name":"negative regulation of acetate degradation","type":"exact"}],"termid":"GO:0045753"}


id: MONDO:0100018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pityriasis rubra pilaris that occurs around the fifth or sixth decade of life.","direct_ancestors":[{"relation_name":"is_a","term_name":"pityriasis rubra pilaris","termid":"MONDO:0100017"}],"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":"adult onset pityriasis rubra pilaris","synonyms":[{"name":"adult onset PRP","type":"exact"}],"termid":"MONDO:0100018","xrefs":{"Monarch":{"xref_id":"0100018"}}}


id: MONDO:0002653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A premalignant condition morphologically characterized by the presence of the characteristic Paget cells in the intraepithelial tissue of the penis. It presents as a smooth raised reddish area that may or may not be painful. -- 2003","definition_xrefs":["NCIT:C27817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"penile carcinoma","termid":"MONDO:0006360"},{"relation_name":"is_a","term_name":"extramammary Paget disease","termid":"MONDO:0008177"}],"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":"Paget disease of the penis","secondary_identifiers":["MEDGEN:66374","GARD:21638","SCTID:398768004","UMLS:C0221286","DOID:3448","Orphanet:398053"],"synonyms":[{"name":"Paget disease of the penis","type":"exact"},{"name":"Paget's disease of penis","type":"exact"},{"name":"Paget's disease of the penis","type":"exact"},{"name":"adenocarcinoma of penis","type":"exact"},{"name":"adenocarcinoma of the penis","type":"related"},{"name":"penile adenocarcinoma","type":"exact"},{"name":"penis Paget disease","type":"exact"},{"name":"penis Paget's disease","type":"related"},{"name":"penis adenocarcinoma","type":"exact"},{"name":"penis mammary Paget's disease","type":"exact"}],"termid":"MONDO:0002653","xrefs":{"Monarch":{"xref_id":"0002653"}}}


id: PBO:0066062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rap guanine nucleotide exchange factor 6","termid":"PBO:0066062"}


id: PBO:0049098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPR155 divergent transcript","termid":"PBO:0049098"}


id: MONDO:0019173
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rabies is a viral zoonosis leading to a fatal encephalopathy if not treated.","definition_xrefs":["Orphanet:770"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease","termid":"MONDO:0005108"},{"relation_name":"is_a","term_name":"infectious disorder of the nervous system","termid":"MONDO:0020010"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rabies","secondary_identifiers":["NORD:1644","SCTID:14168008","MedDRA:10037742","MEDGEN:48308","UMLS:C0034494","MESH:D011818","DOID:11260","ICD9:071","GARD:7516","ICD10CM:A82","NCIT:C28182","icd11.foundation:854762584"],"synonyms":[{"name":"lyssa","type":"exact"}],"termid":"MONDO:0019173","xrefs":{"Monarch":{"xref_id":"0019173"}}}


id: PBO:0059118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monooxygenase DBH like 2, pseudogene","termid":"PBO:0059118"}


id: PBO:0005663
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by Thi5","termid":"PBO:0005663"}


id: SO:0100005
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A motif of 4 consecutive residues with dihedral angles as follows: res i: phi -90 bounds -120 to -60, res i psi -10 bounds -50 to 30, res i+1: phi -90 bounds -120 to -60, res i+1: psi -10 bounds -50 to 30, res i+2: phi -75 bounds -100 to -50, res i+2: psi 140 bounds 110 to 170. The extra restriction of the length of the O to O distance is similar, that it be less than 5 Angstrom. In this case these two Oxygen atoms are the main chain carbonyl oxygen atoms of residues i-1 and i+2.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_secondary_structure","termid":"SO:0001078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"catmat_left_handed_four","synonyms":[{"name":"catmat-4l","type":"exact"}],"termid":"SO:0100005"}


id: GO:2000211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glutamate metabolic process.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glutamine family amino acid metabolic process","termid":"GO:0000820"},{"relation_name":"regulates","term_name":"glutamate metabolic process","termid":"GO:0006536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"regulation of glutamate metabolic process","synonyms":[{"name":"regulation of glutamate metabolism","type":"exact"},{"name":"regulation of glutamic acid metabolic process","type":"exact"},{"name":"regulation of glutamic acid metabolism","type":"exact"}],"termid":"GO:2000211"}


id: FYPO:0007489
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the Golgi apparatus is decreased, and the protein is present in the cytosol instead.","definition_xrefs":["PomBase:mah","PMID:32918581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to Golgi apparatus","termid":"FYPO:0004786"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein localization to Golgi apparatus, with protein mislocalized to cytosol","synonyms":[{"name":"decreased protein localisation to Golgi apparatus, with protein mislocalised to cytosol","type":"exact"},{"name":"decreased protein localization to Golgi apparatus, with protein mislocalized to cytosol during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to Golgi apparatus, with protein mislocalized to cytosol during vegetative growth","type":"exact"},{"name":"reduced protein localization to Golgi apparatus, with protein mislocalized to cytosol","type":"exact"}],"termid":"FYPO:0007489"}


id: PBO:0075855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family member 4","termid":"PBO:0075855"}


id: PBO:0049393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP binding protein 8 (putative)","termid":"PBO:0049393"}


id: PBO:0083448
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; partially overlaps the verified gene BUD31","termid":"PBO:0083448"}


id: MONDO:0024182
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"beriberi","termid":"MONDO:0006676"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dry beriberi","secondary_identifiers":["icd11.foundation:582233757","MEDGEN:541401","UMLS:C0268670","DOID:0070318"],"synonyms":[{"name":"endemic neuritis","type":"related"}],"termid":"MONDO:0024182","xrefs":{"Monarch":{"xref_id":"0024182"}}}


id: PBO:0065510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoseryl-tRNA kinase","termid":"PBO:0065510"}


id: GO:1990046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Merging of two or more mitochondria within a cell to form a single compartment, as a result of a disturbance in cellular homeostasis.","definition_xrefs":["GOC:lb","PMID:19360003"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial fusion","termid":"GO:0008053"},{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007005","GO:0008150"],"is_obsolete":false,"name":"stress-induced mitochondrial fusion","synonyms":[{"name":"SIMH","type":"narrow"},{"name":"mitochondrial fusion in response to stress","type":"related"},{"name":"stress-induced mitochondrial hyperfusion","type":"narrow"}],"termid":"GO:1990046"}


id: PBO:0045826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 16","termid":"PBO:0045826"}


id: PBO:0034118
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-helper_property","termid":"PBO:0034118"}


id: PBO:0043861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cramped chromatin regulator homolog 1","termid":"PBO:0043861"}


id: PBO:0017964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylenetetrahydrofolate reductase Mtd1 (predicted)","termid":"PBO:0017964"}


id: PBO:0005294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACN9 family protein","termid":"PBO:0005294"}


id: PBO:0047230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 230 member B","termid":"PBO:0047230"}


id: PR:Q09927
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- aca1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09927"],"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":"L-azetidine-2-carboxylic acid acetyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC21E11.04","synonyms":[{"name":"Spom972h-aca1","type":"exact"}],"termid":"PR:Q09927"}


id: PBO:0086760
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; regulated by the metal-responsive Aft1p transcription factor; highly inducible in zinc-depleted conditions; localizes to the soluble fraction; SWAT-GFP and mCherry fusion proteins localize to the endoplasmic reticulum and vacuole respectively; YOR387C has a paralog, VEL1, that arose from a single-locus duplication","termid":"PBO:0086760"}


id: GO:0060062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of the specialized region at the dorsal lip of the blatopore of the embryo that acts as the main signaling center establishing the vertebrate body plan.","definition_xrefs":["GOC:dph","PMID:9442883"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Spemann organizer formation","termid":"GO:0060061"}],"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":"Spemann organizer formation at the dorsal lip of the blastopore","synonyms":[{"name":"Spemann's organizer formation at the dorsal lip of the blastopore","type":"exact"},{"name":"Spemann-Mangold organizer formation at the dorsal lip of the blastopore","type":"exact"}],"termid":"GO:0060062"}


id: PBO:0013789
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae TPS1","termid":"PBO:0013789"}


id: GO:1904256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of an iron transmembrane transporter activity.","definition_xrefs":["GOC:TermGenie","PMID:15514116","GOC:BHF","GOC:kom","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of iron ion transmembrane transporter activity (obsolete GO:1904256)","synonyms":[{"name":"activation of iron cation channel activity","type":"narrow"},{"name":"activation of iron channel activity","type":"narrow"},{"name":"activation of iron-specific channel activity","type":"narrow"},{"name":"positive regulation of iron cation channel activity","type":"exact"},{"name":"positive regulation of iron channel activity","type":"exact"},{"name":"positive regulation of iron transmembrane transporter activity","type":"exact"},{"name":"positive regulation of iron-specific channel activity","type":"exact"},{"name":"up regulation of iron cation channel activity","type":"exact"},{"name":"up regulation of iron channel activity","type":"exact"},{"name":"up regulation of iron-specific channel activity","type":"exact"},{"name":"up-regulation of iron cation channel activity","type":"exact"},{"name":"up-regulation of iron channel activity","type":"exact"},{"name":"up-regulation of iron-specific channel activity","type":"exact"},{"name":"upregulation of iron cation channel activity","type":"exact"},{"name":"upregulation of iron channel activity","type":"exact"},{"name":"upregulation of iron-specific channel activity","type":"exact"}],"termid":"GO:1904256"}


id: FYPO:0005961
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which a meiotic spindle forms with microtubules emanating from three or more poles.","definition_xrefs":["PomBase:mah","PMID:15992541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle","termid":"FYPO:0000734"},{"relation_name":"is_a","term_name":"multipolar spindle","termid":"FYPO:0005959"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0002399"}],"interesting_parent_ids":["FYPO:0000120","FYPO:0000054","FYPO:0005447","FYPO:0000002","FYPO:0002399","FYPO:0001985"],"is_obsolete":false,"name":"multipolar meiotic spindle","synonyms":[{"name":"multipolar meiotic spindles","type":"exact"},{"name":"multipolar spindle during meiosis","type":"exact"}],"termid":"FYPO:0005961"}


id: FYPO:0006300
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at centromere inner repeat regions is increased.","definition_xrefs":["PomBase:mah","PMID:16797182"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to chromatin during vegetative growth","termid":"FYPO:0003011"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"increased protein localization to chromatin at centromere inner repeat","synonyms":[{"name":"increased protein localisation to chromatin at centromere inner repeat","type":"exact"},{"name":"increased protein localization to chromatin at centromere imr","type":"exact"},{"name":"increased protein localization to chromatin at centromere inner repeat during mitotic cell cycle","type":"related"},{"name":"increased protein localization to chromatin at centromere inner repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0006300"}


id: FYPO:0009111
data:
  {"alleles_by_uniquename":{"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118960],"is_not":false,"summary":null,"term":"FYPO:0009111"}]},"cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population phenotype that reflects increased occurrence of flocculation. Flocculation is the non-sexual aggregation of single cells.","definition_xrefs":["PMID:35924983"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased flocculation","termid":"FYPO:0000155"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02527":null},"genotype_count":1,"genotypes_by_uniquename":{"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown":{"display_name":"lig4::KanMX6(RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"increased flocculation during vegetative growth","references_by_uniquename":{"PMID:37233261":null},"single_locus_annotated_genes":["SJAG_02527"],"single_locus_genotype_uniquenames":["lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown"],"termid":"FYPO:0009111","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000081":null,"FYPO:0009111":null}}


id: GO:0034811
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: benzo(a)pyrene + O2 = benzo(a)pyrene-cis-9,10-dihydrodiol.","definition_xrefs":["UM-BBD_reactionID:r1132"],"gene_count":0,"genotype_count":0,"name":"obsolete benzo(a)pyrene 9,10-dioxygenase activity (obsolete GO:0034811)","termid":"GO:0034811"}


id: PBO:0078060
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 50","termid":"PBO:0078060"}


id: FYPO:0004749
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 heterochromatin is assembled over a larger portion of the subtelomeric region of the chromosome than normal.","definition_xrefs":["GO:0031509","PMID:25774602","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased spatial extent of heterochromatin assembly","termid":"FYPO:0007953"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000641","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased spatial extent of subtelomeric heterochromatin assembly","synonyms":[{"name":"increased spatial extent of heterochromatin assembly at subtelomere","type":"exact"},{"name":"increased spatial extent of subtelomeric heterochromatin assembly during mitotic cell cycle","type":"related"},{"name":"increased spatial extent of subtelomeric heterochromatin assembly during vegetative growth","type":"exact"},{"name":"increased spatial extent of subtelomeric heterochromatin formation","type":"exact"},{"name":"increased spatial extent of telomeric heterochromatin assembly","type":"related"},{"name":"subtelomeric heterochromatin spreading","type":"related"}],"termid":"FYPO:0004749"}


id: PBO:0001383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Polo kinase Plo1","termid":"PBO:0001383"}


id: GO:1902926
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving inulin.","definition_xrefs":["GO_REF:0000068","GOC:TermGenie","PMID:23104410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fructan metabolic process","termid":"GO:0010145"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"inulin metabolic process","synonyms":[{"name":"inulin metabolism","type":"exact"}],"termid":"GO:1902926"}


id: PBO:0032736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post-Golgi vesicle-mediated transport protein Avl9 (predicted)","termid":"PBO:0032736"}


id: PBO:0011460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trancriptional repressor protein BolA domain (predicted)","termid":"PBO:0011460"}


id: PR:Q10329
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pre6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10329"],"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":"proteasome subunit alpha type-4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC106.16","synonyms":[{"name":"Spom972h-pre6","type":"exact"}],"termid":"PR:Q10329"}


id: GO:0031307
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the mitochondrial outer membrane consisting of the gene products having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of mitochondrial outer membrane (obsolete GO:0031307)","synonyms":[{"name":"integral to mitochondrial outer membrane","type":"narrow"}],"termid":"GO:0031307"}


id: GO:0008523
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: multivitamin(out) + Na+(out) = multivitamin(in) + Na+(in). Multivitamins include pantothenate, biotin and lipoate.","definition_xrefs":["TC:2.A.21.5.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:sodium symporter activity","termid":"GO:0015370"},{"relation_name":"is_a","term_name":"vitamin transmembrane transporter activity","termid":"GO:0090482"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"sodium-dependent multivitamin transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-429581","Reactome:R-HSA-199206","Reactome:R-HSA-199219"],"termid":"GO:0008523"}


id: MONDO:0006472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tracheal carcinoma (obsolete MONDO:0006472)","termid":"MONDO:0006472","xrefs":{"Monarch":{"xref_id":"0006472"}}}


id: MONDO:0004814
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete vascular skin disease (obsolete MONDO:0004814)","termid":"MONDO:0004814","xrefs":{"Monarch":{"xref_id":"0004814"}}}


id: GO:0140561
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-alpha-D-glucose + [protein with EGF-like domain]-L-serine = UDP + [protein with EGF-like domain]-3-O-(beta-D-glucosyl)-L-serine.","definition_xrefs":["RHEA:58116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"EGF-domain serine glucosyltransferase activity","secondary_identifiers":["EC:2.4.1.376"],"termid":"GO:0140561"}


id: GO:0016103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of diterpenoid compounds, terpenoids with four isoprene units.","definition_xrefs":["ISBN:0198547684","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diterpenoid metabolic process","termid":"GO:0016101"},{"relation_name":"is_a","term_name":"terpenoid catabolic process","termid":"GO:0016115"}],"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:0006629","GO:0008150"],"is_obsolete":false,"name":"diterpenoid catabolic process","synonyms":[{"name":"diterpene catabolic process","type":"narrow"},{"name":"diterpene catabolism","type":"narrow"},{"name":"diterpenoid breakdown","type":"exact"},{"name":"diterpenoid catabolism","type":"exact"},{"name":"diterpenoid degradation","type":"exact"}],"termid":"GO:0016103"}


id: GO:0000316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of sulfite into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound transport","termid":"GO:0072348"},{"relation_name":"is_a","term_name":"inorganic anion transmembrane transport","termid":"GO:0098661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"sulfite transmembrane transport","synonyms":[{"name":"sulphite transport","type":"exact"}],"termid":"GO:0000316"}


id: GO:0038137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals transmitted by a heterodimeric complex of the tyrosine kinase receptors EGFR (epidermal growth factor receptor/ERBB1) and ERBB4. The pathway begins with binding of a ligand to either cell surface receptor, or the dimeric receptor complex, and ends with regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:16460914","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal growth factor receptor signaling pathway","termid":"GO:0007173"},{"relation_name":"is_a","term_name":"ERBB4 signaling pathway","termid":"GO:0038130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"ERBB4-EGFR signaling pathway","synonyms":[{"name":"ERBB1-ERBB4 signaling pathway","type":"exact"},{"name":"ERBB4-EGFR signalling pathway","type":"exact"},{"name":"HER1-HER4 signaling pathway","type":"exact"}],"termid":"GO:0038137"}


id: GO:0009467
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete monoheme class I cytochrome c (obsolete GO:0009467)","synonyms":[{"name":"monoheme class I cytochrome c","type":"exact"}],"termid":"GO:0009467"}


id: PBO:0038718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin gamma 1 pseudogene 13","termid":"PBO:0038718"}


id: PBO:0068541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 146, pseudogene","termid":"PBO:0068541"}


id: PBO:0041000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"boule homolog, RNA binding protein","termid":"PBO:0041000"}


id: GO:0060397
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which STAT proteins (Signal Transducers and Activators of Transcription) are activated by members of the JAK (janus activated kinase) family of tyrosine kinases, following the binding of physiological ligands to the growth hormone receptor. Once activated, STATs dimerize and translocate to the nucleus and modulate the expression of target genes.","definition_xrefs":["PMID:11445442","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth hormone receptor signaling pathway","termid":"GO:0060396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"growth hormone receptor signaling pathway via JAK-STAT","secondary_identifiers":["Reactome:R-HSA-982772"],"synonyms":[{"name":"JAK-STAT cascade involved in growth hormone signalling pathway","type":"exact"}],"termid":"GO:0060397"}


id: PBO:0072155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 32","termid":"PBO:0072155"}


id: FYPO:0003130
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which entry into the G1 phase of the mitotic cell cycle (exit from mitosis) begins earlier than normal during a cellular response to ionizing radiation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"premature mitotic G1 phase entry","termid":"FYPO:0000828"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000631"],"is_obsolete":false,"name":"premature mitotic G1 phase entry during cellular response to ionizing radiation","synonyms":[{"name":"accelerated entry into G1 during cellular response to ionizing radiation","type":"related"},{"name":"advanced mitotic G1 phase entry during cellular response to ionizing radiation","type":"exact"},{"name":"mitotic cell cycle advance in G1 during cellular response to ionizing radiation","type":"related"},{"name":"premature G1 phase entry during cellular response to ionizing radiation during mitotic cell cycle","type":"exact"},{"name":"premature exit from mitosis during cellular response to ionizing radiation","type":"exact"},{"name":"premature mitotic G1 phase entry during cellular response to IR","type":"exact"},{"name":"premature mitotic G1 phase entry during cellular response to ionizing radiation during vegetative growth","type":"exact"},{"name":"premature mitotic G1 progression during cellular response to ionizing radiation","type":"related"}],"termid":"FYPO:0003130"}


id: GO:0071465
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 desiccation stimulus, extreme dryness resulting from the prolonged deprivation of water.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to desiccation","termid":"GO:0009269"},{"relation_name":"is_a","term_name":"cellular response to water deprivation","termid":"GO:0042631"}],"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 desiccation","synonyms":[{"name":"desiccation tolerance","type":"related"}],"termid":"GO:0071465"}


id: PATO:0001444
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A broken quality inhering in a bearer by virtue of the bearer's being broken open.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"wholeness","termid":"PATO:0001442"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"broken","secondary_identifiers":["PATO:0001443","PATO:0001820"],"synonyms":[{"name":"burst","type":"exact"},{"name":"cracked","type":"related"},{"name":"fractured","type":"exact"},{"name":"fragmented","type":"exact"},{"name":"hemorrhaged","type":"related"},{"name":"ruptured","type":"exact"},{"name":"split","type":"related"},{"name":"torn","type":"related"}],"termid":"PATO:0001444"}


id: PBO:0077359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 98","termid":"PBO:0077359"}


id: PBO:0052624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 3","termid":"PBO:0052624"}


id: PBO:0054828
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 2241","termid":"PBO:0054828"}


id: GO:0047866
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N,N-dimethylglycine + H2O + O2 = formaldehyde + H2O2 + sarcosine.","definition_xrefs":["EC:1.5.3.10","RHEA:17077"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor","termid":"GO:0016647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"dimethylglycine oxidase activity","secondary_identifiers":["MetaCyc:DIMETHYLGLYCINE-OXIDASE-RXN","KEGG_REACTION:R01564"],"synonyms":[{"name":"N,N-dimethylglycine:oxygen oxidoreductase (demethylating)","type":"related"}],"termid":"GO:0047866"}


id: PBO:0056913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane integral NOTCH2 associated receptor 2","termid":"PBO:0056913"}


id: GO:0060333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interferon-gamma binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription. Interferon gamma is the only member of the type II interferon found so far.","definition_xrefs":["GOC:signaling","GOC:add","PMID:28901902","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interferon-mediated signaling pathway","termid":"GO:0140888"},{"relation_name":"part_of","term_name":"cellular response to type II interferon","termid":"GO:0071346"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"type II interferon-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-877300"],"synonyms":[{"name":"gamma-interferon-mediated signaling pathway","type":"exact"},{"name":"immune interferon signaling pathway","type":"exact"},{"name":"interferon-gamma-mediated signaling pathway","type":"exact"},{"name":"interferon-gamma-mediated signalling pathway","type":"exact"},{"name":"type II IFN-mediated signaling pathway","type":"exact"}],"termid":"GO:0060333"}


id: PBO:0002355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal protein Adg2","termid":"PBO:0002355"}


id: PBO:0082805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of U2 snRNP complex; disruption causes reduced U2 snRNP levels; physically interacts with Msl1p; putative homolog of human U2A' snRNP protein","termid":"PBO:0082805"}


id: GO:0002902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of B cell apoptotic process.","definition_xrefs":["GOC:add","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lymphocyte apoptotic process","termid":"GO:0070228"},{"relation_name":"regulates","term_name":"B cell apoptotic process","termid":"GO:0001783"}],"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 B cell apoptotic process","synonyms":[{"name":"regulation of B cell apoptosis","type":"narrow"}],"termid":"GO:0002902"}


id: PATO:0001219
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001219 area_unit (obsolete PATO:0001219)","termid":"PATO:0001219"}


id: PBO:0033754
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_proteolysis_during_vegetative_growth","termid":"PBO:0033754"}


id: PBO:0074226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC45A4 antisense RNA 1","termid":"PBO:0074226"}


id: PR:O59807
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC550.09 gene.","definition_xrefs":["UniProtKB:O59807","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":"peroxisomal membrane protein pex32 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC550.09","synonyms":[{"name":"Spom972h-SPCC550.09","type":"exact"},{"name":"peroxin-32 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O59807"}


id: PBO:0063058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PITX2 adjacent non-coding RNA","termid":"PBO:0063058"}


id: PBO:0064581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POTE ankyrin domain family member B3","termid":"PBO:0064581"}


id: MONDO:0020105
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies (obsolete MONDO:0020105)","secondary_identifiers":["Orphanet:98370","icd11.foundation:2071787420"],"termid":"MONDO:0020105","xrefs":{"Monarch":{"xref_id":"0020105"}}}


id: MONDO:1012193
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thalamic-cerebellar neuropathy, non-human animal","termid":"MONDO:1011854"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thalamic-cerebellar neuropathy, sheep","secondary_identifiers":["OMIA:000723-9940"],"termid":"MONDO:1012193","xrefs":{"Monarch":{"xref_id":"1012193"}}}


id: PBO:0000640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF and RSC complex subunit Ssr3","termid":"PBO:0000640"}


id: GO:1904883
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of telomerase catalytic core complex assembly.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:BHF_telomere","GOC:BHF","GOC:rph","PMID:26586433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein-containing complex assembly","termid":"GO:0031333"},{"relation_name":"is_a","term_name":"regulation of telomerase catalytic core complex assembly","termid":"GO:1904882"},{"relation_name":"negatively_regulates","term_name":"telomerase catalytic core complex assembly","termid":"GO:1904868"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0065003"],"is_obsolete":false,"name":"negative regulation of telomerase catalytic core complex assembly","synonyms":[{"name":"down regulation of TERT-TERC complex assembly","type":"related"},{"name":"down regulation of TERT-TERC complex formation","type":"related"},{"name":"down regulation of telomerase catalytic core complex assembly","type":"exact"},{"name":"down regulation of telomerase catalytic core complex formation","type":"exact"},{"name":"down-regulation of TERT-TERC complex assembly","type":"related"},{"name":"down-regulation of TERT-TERC complex formation","type":"related"},{"name":"down-regulation of telomerase catalytic core complex assembly","type":"exact"},{"name":"down-regulation of telomerase catalytic core complex formation","type":"exact"},{"name":"downregulation of TERT-TERC complex assembly","type":"related"},{"name":"downregulation of TERT-TERC complex formation","type":"related"},{"name":"downregulation of telomerase catalytic core complex assembly","type":"exact"},{"name":"downregulation of telomerase catalytic core complex formation","type":"exact"},{"name":"inhibition of TERT-TERC complex assembly","type":"related"},{"name":"inhibition of TERT-TERC complex formation","type":"related"},{"name":"inhibition of telomerase catalytic core complex assembly","type":"narrow"},{"name":"inhibition of telomerase catalytic core complex formation","type":"narrow"},{"name":"negative regulation of TERT-TERC complex assembly","type":"related"},{"name":"negative regulation of TERT-TERC complex formation","type":"related"},{"name":"negative regulation of telomerase catalytic core complex formation","type":"exact"}],"termid":"GO:1904883"}


id: MONDO:0001087
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by an enduring pattern of inability to establish close relationships coupled with cognitive or perceptual distortions, odd beliefs and speech, and eccentric behavior and appearance.","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":"schizotypal personality disorder","secondary_identifiers":["MESH:D012569","ICD9:301.22","NCIT:C92632","MEDGEN:1826899","UMLS:C1443045","DOID:10646","SCTID:31027006"],"termid":"MONDO:0001087","xrefs":{"Monarch":{"xref_id":"0001087"}}}


id: MONDO:0013929
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the TSPEAR gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 98","secondary_identifiers":["MEDGEN:766846","GARD:22644","OMIM:614861","DOID:0110540","UMLS:C3553932"],"synonyms":[{"name":"DFNB98","type":"narrow"},{"name":"TSPEAR autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 98","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 98","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in TSPEAR","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 98","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 98","type":"exact"},{"name":"deafness, autosomal recessive 98","type":"narrow"},{"name":"deafness, autosomal recessive type 98","type":"narrow"}],"termid":"MONDO:0013929","xrefs":{"Monarch":{"xref_id":"0013929"}}}


id: PBO:0081029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger CCCH-type containing 11A","termid":"PBO:0081029"}


id: PBO:0054333
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 1726","termid":"PBO:0054333"}


id: GO:0102330
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: malonyl-CoA + a palmitoyl-[acp] = 1-heptadecene + 2 carbon dioxide + coenzyme A + a holo-[acyl-carrier protein].","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete palmitoyl-[acp] elongase/decarboxylase activity (obsolete GO:0102330)","termid":"GO:0102330"}


id: GO:1902234
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of positive thymic T cell selection.","definition_xrefs":["PMID:22080863","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of T cell differentiation in thymus","termid":"GO:0033089"},{"relation_name":"is_a","term_name":"regulation of positive thymic T cell selection","termid":"GO:1902232"},{"relation_name":"positively_regulates","term_name":"positive thymic T cell selection","termid":"GO:0045059"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"positive regulation of positive thymic T cell selection","synonyms":[{"name":"activation of positive thymic T cell selection","type":"narrow"},{"name":"activation of positive thymic T lymphocyte selection","type":"narrow"},{"name":"activation of positive thymic T-cell selection","type":"narrow"},{"name":"activation of positive thymic T-lymphocyte selection","type":"narrow"},{"name":"positive regulation of positive thymic T lymphocyte selection","type":"exact"},{"name":"positive regulation of positive thymic T-cell selection","type":"exact"},{"name":"positive regulation of positive thymic T-lymphocyte selection","type":"exact"},{"name":"up regulation of positive thymic T cell selection","type":"exact"},{"name":"up regulation of positive thymic T lymphocyte selection","type":"exact"},{"name":"up regulation of positive thymic T-cell selection","type":"exact"},{"name":"up regulation of positive thymic T-lymphocyte selection","type":"exact"},{"name":"up-regulation of positive thymic T cell selection","type":"exact"},{"name":"up-regulation of positive thymic T lymphocyte selection","type":"exact"},{"name":"up-regulation of positive thymic T-cell selection","type":"exact"},{"name":"up-regulation of positive thymic T-lymphocyte selection","type":"exact"},{"name":"upregulation of positive thymic T cell selection","type":"exact"},{"name":"upregulation of positive thymic T lymphocyte selection","type":"exact"},{"name":"upregulation of positive thymic T-cell selection","type":"exact"},{"name":"upregulation of positive thymic T-lymphocyte selection","type":"exact"}],"termid":"GO:1902234"}


id: PBO:0075119
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 168","termid":"PBO:0075119"}


id: PBO:0109473
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-modified_residue","termid":"PBO:0109473"}


id: GO:0004123
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-cystathionine + H2O = 2-oxobutanoate + L-cysteine + NH4+.","definition_xrefs":["RHEA:14005"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"cystathionine gamma-lyase activity","secondary_identifiers":["GO:0016225","KEGG_REACTION:R01001","MetaCyc:RXN-15130","Reactome:R-HSA-1614583"],"synonyms":[{"name":"L-cystathionine cysteine-lyase (deaminating)","type":"broad"},{"name":"L-cystathionine cysteine-lyase (deaminating; 2-oxobutanoate-forming)","type":"related"},{"name":"gamma-cystathionase activity","type":"broad"},{"name":"homoserine deaminase activity","type":"related"},{"name":"homoserine deaminase-cystathionase activity","type":"related"},{"name":"homoserine dehydratase activity","type":"related"}],"termid":"GO:0004123"}


id: FYPO:0001080
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of a polysaccharide measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered polysaccharide level during vegetative growth","termid":"FYPO:0001085"},{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased polysaccharide level during vegetative growth","synonyms":[{"name":"decreased cellular polysaccharide level during vegetative growth","type":"exact"},{"name":"decreased polysaccharide accumulation during vegetative growth","type":"related"},{"name":"decreased polysaccharide level during mitotic cell cycle","type":"related"},{"name":"reduced polysaccharide level during vegetative growth","type":"exact"}],"termid":"FYPO:0001080"}


id: MONDO:0008439
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"autosomal dominant complex spastic paraplegia","termid":"MONDO:0015087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559"],"is_obsolete":false,"name":"spastic paraplegia-epilepsy-intellectual disability syndrome","secondary_identifiers":["GARD:4915","MEDGEN:356631","UMLS:C1866854","Orphanet:2816","MESH:C536869","OMIM:182610"],"synonyms":[{"name":"SPEMR","type":"exact"},{"name":"spastic paraplegia epilepsy intellectual disability","type":"related"},{"name":"spastic paraplegia epilepsy mental retardation","type":"related"},{"name":"spastic paraplegia, epilepsy, and intellectual disability","type":"related"},{"name":"spastic paraplegia, epilepsy, and mental retardation","type":"related"},{"name":"spemr","type":"related"}],"termid":"MONDO:0008439","xrefs":{"Monarch":{"xref_id":"0008439"}}}


id: PBO:0000125
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sim Four and mal Two Associated protein","termid":"PBO:0000125"}


id: FYPO:0005635
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the spindle begins later than normal during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:21920317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to meiotic spindle","termid":"FYPO:0006454"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of protein localization to spindle during meiosis I","synonyms":[{"name":"delayed onset of protein localisation to spindle during meiosis I","type":"exact"},{"name":"delayed onset of protein localization to meiosis I spindle","type":"exact"},{"name":"delayed onset of protein localization to meiotic spindle during meiosis I","type":"exact"},{"name":"delayed onset of protein localization to spindle during first meiotic nuclear division","type":"exact"},{"name":"delayed protein localization to spindle during meiosis I","type":"exact"}],"termid":"FYPO:0005635"}


id: MONDO:0000512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ameloblastoma (obsolete MONDO:0000512)","termid":"MONDO:0000512","xrefs":{"Monarch":{"xref_id":"0000512"}}}


id: PBO:0056904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIF4G domain containing","termid":"PBO:0056904"}


id: PBO:0068686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 67, pseudogene","termid":"PBO:0068686"}


id: MONDO:0010006
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sandhoff disease is a lysosomal storage disorder from the GM2 gangliosidosis family and is characterized by central nervous system degeneration.","definition_xrefs":["Orphanet:796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye degenerative disorder","termid":"MONDO:0004884"},{"relation_name":"is_a","term_name":"GM2 gangliosidosis","termid":"MONDO:0017720"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"cerebral lipidosis with dementia","termid":"MONDO:0020143"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005244","MONDO:0002039","MONDO:0002525","MONDO:0005328","MONDO:0005066","MONDO:0002561"],"is_obsolete":false,"name":"Sandhoff disease","secondary_identifiers":["GARD:2521","NANDO:2201200","SCTID:23849003","UMLS:C0036161","MESH:D012497","NCIT:C85052","NORD:1688","DOID:3323","NANDO:1200072","ICD10CM:E75.01","icd11.foundation:708581915","OMIM:268800","MEDGEN:11313"],"synonyms":[{"name":"Beta-hexosaminidase-beta-subunit deficiency","type":"related"},{"name":"GM2 gangliosidosis 0 variant","type":"exact"},{"name":"GM2 gangliosidosis, 0 variant","type":"related"},{"name":"GM2 gangliosidosis, type 2","type":"related"},{"name":"GM2-gangliosidosis, type 2","type":"related"},{"name":"Hexosaminidases A and B deficiency","type":"exact"},{"name":"Hexosaminidases a and B deficiency","type":"related"},{"name":"Sandhoff Jatzkewitz disease","type":"exact"},{"name":"Sandhoff disease","type":"exact"},{"name":"Sandhoff disease, adult type","type":"related"},{"name":"Sandhoff disease, infantile type","type":"related"},{"name":"Sandhoff disease, infantile, juvenile, and adult forms","type":"exact"},{"name":"Sandhoff disease, juvenile type","type":"related"},{"name":"Sandhoff-Jatzkewitz-Pilz disease","type":"related"},{"name":"hexosaminidase A and B deficiency disease","type":"related"},{"name":"total hexosaminidase deficiency","type":"related"}],"termid":"MONDO:0010006","xrefs":{"Monarch":{"xref_id":"0010006"}}}


id: GO:0021838
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation and reception of signals that result in the directional movement of interneuron precursors from the subpallium to the cortex.","definition_xrefs":["GOC:cls","GOC:dgh","GOC:dph","GO_REF:0000021","GOC:jid","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell communication","termid":"GO:0007154"},{"relation_name":"is_a","term_name":"signaling","termid":"GO:0023052"},{"relation_name":"part_of","term_name":"interneuron migration from the subpallium to the cortex","termid":"GO:0021830"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"motogenic signaling involved in interneuron migration from the subpallium to the cortex","synonyms":[{"name":"motogenic signalling involved in interneuron migration from the subpallium to the cortex","type":"exact"}],"termid":"GO:0021838"}


id: PBO:0042088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 157","termid":"PBO:0042088"}


id: FYPO:0006925
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 number of sites at which the protein Rad51 accumulates at or near replication fork barriers is lower than normal.","definition_xrefs":["PMID:31149897","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased number of Rad51 foci at mitotic DNA replication fork barriers","synonyms":[{"name":"decreased number of Rad51 foci at mitotic DNA replication fork barriers during mitotic cell cycle","type":"related"},{"name":"decreased number of Rad51 foci at mitotic DNA replication fork barriers during vegetative growth","type":"related"},{"name":"reduced number of Rad51 foci at mitotic DNA replication fork barriers","type":"exact"}],"termid":"FYPO:0006925"}


id: MOD:01853
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to L-lysinoalanine either by forming a cross-link with peptidyl-cysteine or peptidyl-serine, or by condensation with free serine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified residue that can arise from different natural residues","termid":"MOD:00859"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-lysinoalanine","termid":"MOD:01853"}


id: GO:0050856
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of signaling pathways initiated by the cross-linking of an antigen receptor on a T cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antigen receptor-mediated signaling pathway","termid":"GO:0050854"},{"relation_name":"regulates","term_name":"T cell receptor signaling pathway","termid":"GO:0050852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of T cell receptor signaling pathway","synonyms":[{"name":"regulation of T lymphocyte receptor signaling pathway","type":"exact"},{"name":"regulation of T lymphocyte receptor signalling pathway","type":"exact"},{"name":"regulation of T-cell receptor signaling pathway","type":"exact"},{"name":"regulation of T-cell receptor signalling pathway","type":"exact"},{"name":"regulation of T-lymphocyte receptor signaling pathway","type":"exact"},{"name":"regulation of T-lymphocyte receptor signalling pathway","type":"exact"},{"name":"regulation of TCR signaling pathway","type":"exact"}],"termid":"GO:0050856"}


id: MONDO:0003641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic neoplasm of hematopoietic origin that affects the brain, meninges, or spinal cord. Representative examples include Hodgkin and non-Hodgkin lymphomas, histiocytic tumors, and leukemias.","definition_xrefs":["NCIT:C5503"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"central nervous system cancer","termid":"MONDO:0002714"},{"relation_name":"is_a","term_name":"central nervous system neoplasm","termid":"MONDO:0006130"},{"relation_name":"is_a","term_name":"hematopoietic and lymphoid cell neoplasm","termid":"MONDO:0044881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"central nervous system hematopoietic neoplasm","secondary_identifiers":["UMLS:C1332882","MEDGEN:234101","DOID:5772"],"synonyms":[{"name":"CNS haematopoietic neoplasm","type":"exact"},{"name":"CNS haematopoietic tumour","type":"exact"},{"name":"CNS hematopoietic neoplasm","type":"exact"},{"name":"CNS hematopoietic tumor","type":"exact"},{"name":"central nervous system haematopoietic and lymphoid system neoplasm","type":"exact"},{"name":"central nervous system haematopoietic neoplasms","type":"exact"},{"name":"central nervous system haematopoietic tumour","type":"exact"},{"name":"central nervous system hematologic cancer","type":"related"},{"name":"central nervous system hematopoietic and lymphoid system neoplasm","type":"exact"},{"name":"central nervous system hematopoietic neoplasm","type":"exact"},{"name":"central nervous system hematopoietic neoplasms","type":"exact"},{"name":"central nervous system hematopoietic tumor","type":"exact"},{"name":"haematopoietic and lymphoid system neoplasm of central nervous system","type":"exact"},{"name":"haematopoietic neoplasm of CNS","type":"exact"},{"name":"haematopoietic neoplasm of central nervous system","type":"exact"},{"name":"haematopoietic neoplasm of the CNS","type":"exact"},{"name":"haematopoietic neoplasm of the central nervous system","type":"exact"},{"name":"haematopoietic tumour of central nervous system","type":"exact"},{"name":"haematopoietic tumour of the central nervous system","type":"exact"},{"name":"hematopoietic and lymphoid system neoplasm of central nervous system","type":"exact"},{"name":"hematopoietic neoplasm of CNS","type":"exact"},{"name":"hematopoietic neoplasm of central nervous system","type":"exact"},{"name":"hematopoietic neoplasm of the CNS","type":"exact"},{"name":"hematopoietic neoplasm of the central nervous system","type":"exact"},{"name":"hematopoietic tumor of central nervous system","type":"exact"},{"name":"hematopoietic tumor of the central nervous system","type":"exact"},{"name":"lymphomas and hemopoietic neoplasms of CNS","type":"exact"},{"name":"lymphomas and hemopoietic neoplasms of the CNS","type":"exact"}],"termid":"MONDO:0003641","xrefs":{"Monarch":{"xref_id":"0003641"}}}


id: GO:0003919
data:
  {"annotated_genes":["SJAG_01937"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[113557],"is_not":false,"summary":null,"term":"GO:0003919"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + FMN = diphosphate + FAD.","definition_xrefs":["EC:2.7.7.2","RHEA:17237"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylyltransferase activity","termid":"GO:0070566"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01937":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016779","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"FMN adenylyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R00161","Reactome:R-HSA-196929","MetaCyc:FADSYN-RXN"],"synonyms":[{"name":"ATP:FMN adenylyltransferase activity","type":"exact"},{"name":"FAD diphosphorylase activity","type":"related"},{"name":"FAD pyrophosphorylase activity","type":"related"},{"name":"FAD synthetase activity","type":"related"},{"name":"adenosine triphosphate-riboflavin mononucleotide transadenylase activity","type":"related"},{"name":"adenosine triphosphate-riboflavine mononucleotide transadenylase activity","type":"related"},{"name":"flavin adenine dinucleotide synthetase activity","type":"related"},{"name":"riboflavin adenine dinucleotide pyrophosphorylase activity","type":"related"},{"name":"riboflavin mononucleotide adenylyltransferase activity","type":"related"},{"name":"riboflavine adenine dinucleotide adenylyltransferase activity","type":"related"}],"termid":"GO:0003919","terms_by_termid":{"GO:0003919":null}}


id: MONDO:0700261
data:
  {"annotated_genes":["SJAG_04380"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014007"},{"annotations":[85556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007483"}]},"cv_name":"mondo","definition":"Any type 1 interferonopathies in which the cause of the disease is a variation in the ADAR gene. Individuals with variants in ADAR can present with a variety of phenotypes, including Aicardi-Goutieres syndrome and dyschromatosis symmetrica hereditaria.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"type 1 interferonopathy","termid":"MONDO:0700264"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04380":null},"genotype_count":0,"is_obsolete":false,"name":"ADAR-related type 1 interferonopathy","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0700261","terms_by_termid":{"MONDO:0007483":null,"MONDO:0014007":null},"xrefs":{"Monarch":{"xref_id":"0700261"}}}


id: GO:0072739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an anisomycin stimulus.","definition_xrefs":["GOC:mah"],"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 anisomycin","termid":"GO:0072739"}


id: GO:0038102
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Interacting with an activin receptor complex to reduce the action of another ligand, the agonist. A receptor antagonist does not initiate signaling upon binding to a receptor, but instead blocks an agonist from binding to the receptor.","definition_xrefs":["PMID:15062104","GOC:signaling"],"direct_ancestors":[{"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:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"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:0098772","GO:0140678","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"activin receptor antagonist activity","termid":"GO:0038102"}


id: PBO:0028099
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_DNA_binding_specificity","termid":"PBO:0028099"}


id: PBO:0066202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 17 pseudogene 3","termid":"PBO:0066202"}


id: PBO:0003230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kip3 subfamily","termid":"PBO:0003230"}


id: GO:0010087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of phloem and/or xylem over time, from formation to the mature structure. An example of this process is found in Arabidopsis thaliana.","definition_xrefs":["GOC:mtg_sensu","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue development","termid":"GO:0009888"}],"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":"phloem or xylem histogenesis","synonyms":[{"name":"vascular tissue development","type":"broad"},{"name":"vascular tissue histogenesis","type":"exact"}],"termid":"GO:0010087"}


id: SO:0001073
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Polypeptide region that is localized inside the cytoplasm.","definition_xrefs":["EBIBS:GAR","SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extramembrane_polypeptide_region","termid":"SO:0001072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"cytoplasmic_polypeptide_region","secondary_identifiers":["BS:00145"],"synonyms":[{"name":"cytoplasm_location","type":"exact"},{"name":"cytoplasmic polypeptide region","type":"exact"},{"name":"inside","type":"related"}],"termid":"SO:0001073"}


id: GO:0044166
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membranes of the host cell endoplasmic reticulum.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell cytoplasm part","termid":"GO:0033655"},{"relation_name":"part_of","term_name":"host cell endoplasmic reticulum","termid":"GO:0044165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell endoplasmic reticulum lumen","synonyms":[{"name":"host endoplasmic reticulum lumen","type":"exact"}],"termid":"GO:0044166"}


id: FYPO:0001195
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 galactomannan measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased polysaccharide level during vegetative growth","termid":"FYPO:0001080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased galactomannan level","synonyms":[{"name":"decreased cellular galactomannan level","type":"exact"},{"name":"decreased galactomannan accumulation","type":"related"},{"name":"decreased galactomannan level during mitotic cell cycle","type":"related"},{"name":"decreased galactomannan level during vegetative growth","type":"exact"},{"name":"reduced galactomannan level","type":"exact"}],"termid":"FYPO:0001195"}


id: MONDO:0700231
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any exudative vitreoretinopathy caused by variants in the TSPAN12 gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"exudative vitreoretinopathy","termid":"MONDO:0019516"},{"relation_name":"is_a","term_name":"TSPAN12-related vitreoretinopathy","termid":"MONDO:0100484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005559"],"is_obsolete":false,"name":"TSPAN12-related exudative vitreoretinopathy","synonyms":[{"name":"TSPAN12-related exudative vitreoretinopathy","type":"exact"}],"termid":"MONDO:0700231","xrefs":{"Monarch":{"xref_id":"0700231"}}}


id: MOD:01646
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes or replaces an L-serine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue removal","termid":"MOD:01651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-serine removal","termid":"MOD:01646"}


id: GO:0038022
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an odorant 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:sart","GOC:bf","PMID:21041441"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"},{"relation_name":"is_a","term_name":"olfactory receptor activity","termid":"GO:0004984"}],"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:0003674","GO:0038023"],"is_obsolete":false,"name":"G protein-coupled olfactory receptor activity","synonyms":[{"name":"G-protein coupled odorant receptor activity","type":"exact"},{"name":"G-protein coupled olfactory receptor activity","type":"exact"},{"name":"odorant receptor activity, G-protein coupled","type":"narrow"},{"name":"olfactory receptor activity, G-protein coupled","type":"exact"}],"termid":"GO:0038022"}


id: PBO:0079525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trypsin like peroxisomal matrix peptidase 1","termid":"PBO:0079525"}


id: PBO:0084919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Molecular chaperone of the endoplasmic reticulum lumen; involved in polypeptide translocation and folding; nucleotide exchange factor for the ER lumenal Hsp70 chaperone Kar2p; regulated by the unfolded protein response pathway","termid":"PBO:0084919"}


id: MONDO:0020830
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"diaphragm disorder","termid":"MONDO:0005728"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diaphragmitis","secondary_identifiers":["icd11.foundation:1124735890","MEDGEN:507638","UMLS:C0011985","SCTID:73160007"],"synonyms":[{"name":"diaphragmatitis","type":"exact"},{"name":"diaphragmitis","type":"exact"}],"termid":"MONDO:0020830","xrefs":{"Monarch":{"xref_id":"0020830"}}}


id: GO:0010859
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of a calcium-dependent cysteine-type endopeptidase, any enzyme that hydrolyzes peptide bonds in polypeptides by a mechanism in which the sulfhydryl group of a cysteine residue at the active center acts as a nucleophile in a calcium-dependent manner.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteine-type endopeptidase inhibitor activity","termid":"GO:0004869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0004857"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0140678","GO:0098772","GO:0004857"],"is_obsolete":false,"name":"calcium-dependent cysteine-type endopeptidase inhibitor activity","termid":"GO:0010859"}


id: PBO:0067503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 643, pseudogene","termid":"PBO:0067503"}


id: PBO:0058340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4713 host gene","termid":"PBO:0058340"}


id: GO:0047416
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N-acetylarylalkylamine = acetate + arylalkylamine.","definition_xrefs":["EC:3.5.1.76","MetaCyc:3.5.1.76-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016810","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"arylalkyl acylamidase activity","secondary_identifiers":["RHEA:10352"],"synonyms":[{"name":"N-acetylarylalkylamine amidohydrolase activity","type":"related"},{"name":"aralkyl acylamidase activity","type":"related"}],"termid":"GO:0047416"}


id: PBO:0035950
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_localization_to_centromeric_chromatin_during_mitotic_G1_phase","termid":"PBO:0035950"}


id: GO:0050871
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of B cell activation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of B cell activation","termid":"GO:0050864"},{"relation_name":"is_a","term_name":"positive regulation of lymphocyte activation","termid":"GO:0051251"},{"relation_name":"positively_regulates","term_name":"B cell activation","termid":"GO:0042113"}],"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 B cell activation","synonyms":[{"name":"activation of B cell activation","type":"narrow"},{"name":"positive regulation of B lymphocyte activation","type":"exact"},{"name":"positive regulation of B-cell activation","type":"exact"},{"name":"positive regulation of B-lymphocyte activation","type":"exact"},{"name":"stimulation of B cell activation","type":"narrow"},{"name":"up regulation of B cell activation","type":"exact"},{"name":"up-regulation of B cell activation","type":"exact"},{"name":"upregulation of B cell activation","type":"exact"}],"termid":"GO:0050871"}


id: GO:2000552
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of T-helper 2 cell cytokine production.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell cytokine production","termid":"GO:0002725"},{"relation_name":"is_a","term_name":"negative regulation of type 2 immune response","termid":"GO:0002829"},{"relation_name":"is_a","term_name":"regulation of T-helper 2 cell cytokine production","termid":"GO:2000551"},{"relation_name":"negatively_regulates","term_name":"T-helper 2 cell cytokine production","termid":"GO:0035745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of T-helper 2 cell cytokine production","synonyms":[{"name":"negative regulation of Th2 cell cytokine production","type":"exact"}],"termid":"GO:2000552"}


id: GO:0000332
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Provision of the template used by reverse transcriptase to synthesize the G-rich strand of telomeric DNA.","definition_xrefs":["PMID:11812242","PMID:7958872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA template activity","termid":"GO:0000497"},{"relation_name":"part_of","term_name":"telomerase activity","termid":"GO:0003720"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"part_of","termid":"GO:0016740"},{"rel_name":"part_of","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"part_of","termid":"GO:0016779"},{"rel_name":"part_of","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0140097","GO:0003677","GO:0003824","GO:0005488","GO:0016779","GO:0003674"],"is_obsolete":false,"name":"template for synthesis of G-rich strand of telomere DNA activity","synonyms":[{"name":"telomerase RNA","type":"exact"},{"name":"telomerase, template","type":"exact"}],"termid":"GO:0000332"}


id: GO:0043598
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cytoplasmic complex of two polypeptides that loads the DNA polymerase processivity factor proliferating cell nuclear antigen (PCNA) onto DNA, thereby permitting processive DNA synthesis catalyzed by DNA polymerase. Examples of this component are found in prokaryotic species.","definition_xrefs":["GOC:mtg_sensu","PMID:16172520","PMID:14646196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA replication factor C complex","termid":"GO:0005663"},{"relation_name":"part_of","term_name":"cytoplasmic replisome","termid":"GO:0043600"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0032991","GO:0005694","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"cytoplasmic DNA replication factor C complex","synonyms":[{"name":"cytoplasmic RFC","type":"exact"},{"name":"cytoplasmic clamp loader","type":"exact"}],"termid":"GO:0043598"}


id: PBO:0034163
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-releases_neurotransmitter","termid":"PBO:0034163"}


id: MONDO:0005387
data:
  {"annotated_genes":["SJAG_03720","SJAG_00103","SJAG_04114","SJAG_03698","SJAG_02690","SJAG_03418","SJAG_04950","SJAG_04148","SJAG_04738","SJAG_02954","SJAG_02294","SJAG_04703","SJAG_02339","SJAG_03051","SJAG_00377"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008840"},{"annotations":[85492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009258"},{"annotations":[86481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030736"},{"annotations":[85167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013689"},{"annotations":[85926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054850"},{"annotations":[86727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013972"},{"annotations":[85537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014126"},{"annotations":[85153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014843"},{"annotations":[85944,85943],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054862"},{"annotations":[85238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030870"},{"annotations":[85640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958035"},{"annotations":[86535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010350"},{"annotations":[86128,86129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014321"}]},"cv_name":"mondo","definition":"Absent or premature cessation of ovarian function due to a pathologic process originating within the ovaries.","definition_xrefs":["NCIT:C113352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian dysfunction","termid":"MONDO:0001889"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00103":null,"SJAG_00377":null,"SJAG_02294":null,"SJAG_02339":null,"SJAG_02690":null,"SJAG_02954":null,"SJAG_03051":null,"SJAG_03418":null,"SJAG_03698":null,"SJAG_03720":null,"SJAG_04114":null,"SJAG_04148":null,"SJAG_04703":null,"SJAG_04738":null,"SJAG_04950":null},"genotype_count":0,"is_obsolete":false,"name":"primary ovarian failure","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0004266","ICD9:253.4","SCTID:370999003","DOID:5426","ICD10CM:E28.3","MESH:D016649","NANDO:2100139","Orphanet:619","UMLS:C0085215","MEDGEN:38820","SCTID:65846009","ICD9:256.39"],"synonyms":[{"name":"female hypergonadotropic hypogonadism","type":"related"},{"name":"hypergonadotrophic ovarian failure","type":"related"},{"name":"hypergonadotropic hypogonadism","type":"related"},{"name":"hypergonadotropic hypogonadism (female)","type":"related"},{"name":"premature menopause","type":"related"},{"name":"premature ovarian failure","type":"related"},{"name":"premature ovarian insufficiency","type":"related"},{"name":"primary female hypogonadism","type":"related"},{"name":"primary ovarian failure","type":"exact"},{"name":"primary ovarian insufficiency","type":"exact"}],"termid":"MONDO:0005387","terms_by_termid":{"MONDO:0008840":null,"MONDO:0009258":null,"MONDO:0010350":null,"MONDO:0013689":null,"MONDO:0013972":null,"MONDO:0014126":null,"MONDO:0014321":null,"MONDO:0014843":null,"MONDO:0030736":null,"MONDO:0030870":null,"MONDO:0054850":null,"MONDO:0054862":null,"MONDO:0958035":null},"xrefs":{"Monarch":{"xref_id":"0005387"}}}


id: PBO:0041322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 74","termid":"PBO:0041322"}


id: GO:0023049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a protein/peptide signal causes activation of a receptor.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signal initiation by protein/peptide mediator (obsolete GO:0023049)","synonyms":[{"name":"signal initiation by protein/peptide mediator","type":"exact"}],"termid":"GO:0023049"}


id: GO:0052562
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or disrupts the normal execution of an immune response of the host organism. The immune response is any immune system process that functions in the calibrated response of an organism to a potential internal or invasive threat. 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 perturbation of host immune response","termid":"GO:0052553"}],"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 immune response","secondary_identifiers":["GO:0052561"],"synonyms":[{"name":"down regulation by symbiont of host immune response","type":"exact"},{"name":"down-regulation by symbiont of host immune response","type":"exact"},{"name":"downregulation by symbiont of host immune response","type":"exact"},{"name":"inhibition by symbiont of host immune response","type":"narrow"},{"name":"negative regulation by organism of immune response of other organism involved in symbiotic interaction","type":"broad"},{"name":"negative regulation by symbiont of host immune response","type":"exact"},{"name":"suppression by symbiont of host immune response","type":"exact"}],"termid":"GO:0052562"}


id: PBO:0087205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-adenosylmethionine-dependent lysine methyltransferase; involved in the trimethylation of eEF1A (Tef1p/Tef2p) at lysine 79; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; required for replication of Brome mosaic virus in budding yeast; expresses a circular RNA; originally misclassified as a N-6-adenine specific DNA methyltransferase based on sequence similarity; both Efm5p and human ortholog N6AMT2 can methylate eEF1a from either species in vitro","termid":"PBO:0087205"}


id: MONDO:0019340
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Scleroderma is a rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and, sometimes, other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc).","definition_xrefs":["Orphanet:801"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rheumatic disorder","termid":"MONDO:0005554"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"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":"scleroderma","secondary_identifiers":["MEDGEN:3770","NCIT:C26746","DOID:419","UMLS:C0011644","EFO:1001993","HP:0100324","GARD:18705","MedDRA:10039710"],"synonyms":[{"name":"dermatosclerosis","type":"exact"},{"name":"scleroderma","type":"exact"},{"name":"scleroderma (disease)","type":"exact"}],"termid":"MONDO:0019340","xrefs":{"Monarch":{"xref_id":"0019340"}}}


id: PBO:0004855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sporulation specific 1,3-beta-glucanosyltransferase Gas4","termid":"PBO:0004855"}


id: PBO:0041650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel auxiliary subunit alpha2delta 4","termid":"PBO:0041650"}


id: PBO:0079061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon TAC) 1-2","termid":"PBO:0079061"}


id: PBO:0036186
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K4_dimethylation_at_centromere_outer_repeat_during_vegetative_growth","termid":"PBO:0036186"}


id: PBO:0018235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minus-end directed microtubule motor kinesin-14, Klp2","termid":"PBO:0018235"}


id: PBO:0046674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESX homeobox 1","termid":"PBO:0046674"}


id: PBO:0081741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 671","termid":"PBO:0081741"}


id: PR:P36631
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transcription factor ste11 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PomBase:MAH","PMID:11702950"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription factor ste11","termid":"PR:000027538"},{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor ste11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC32C12.02","secondary_identifiers":["PR:000027539","UniProtKB:P36631"],"synonyms":[{"name":"SPBC32C12.02","type":"related"},{"name":"Spom972h-ste11","type":"exact"}],"termid":"PR:P36631"}


id: PBO:0061219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein 10","termid":"PBO:0061219"}


id: MONDO:0015731
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"High anorectal malformation is a rare, genetic, non-syndromic subtype of anorectal malformation, resulting from a developmental defect during embryogenesis, characterized by a wide spectrum of anorectal anomalies, with or without a rectourogenital fistula, located above the pubococcygeal line (i.e. anorectal agenesis, rectal agenesis, atresia, or stenosis). Patients may present with meconuria, pyuria, strangury, and fecal and urinary incontinence.","definition_xrefs":["Orphanet:171201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high anorectal malformation","secondary_identifiers":["MEDGEN:576820","ICD9:751.5","SCTID:253771003","UMLS:C0345210","icd11.foundation:1409973552"],"termid":"MONDO:0015731","xrefs":{"Monarch":{"xref_id":"0015731"}}}


id: GO:0048137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The meiotic divisions undergone by the primary and secondary spermatocytes to produce haploid spermatids.","definition_xrefs":["GOC:pr","ISBN:0879694238","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell division","termid":"GO:0051301"},{"relation_name":"part_of","term_name":"spermatogenesis","termid":"GO:0007283"}],"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":"spermatocyte division","synonyms":[{"name":"spermatocyte cell division","type":"exact"}],"termid":"GO:0048137"}


id: GO:0033265
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to choline, the amine 2-hydroxy-N,N,N-trimethylethanaminium.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"}],"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:0005488","GO:0003674"],"is_obsolete":false,"name":"choline binding","termid":"GO:0033265"}


id: GO:0003384
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The actin-mediated process that results in the contraction of the apical end of a polarized columnar epithelial cell, contributing to the process of gastrulation.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apical constriction","termid":"GO:0003383"},{"relation_name":"part_of","term_name":"epithelial cell morphogenesis involved in gastrulation","termid":"GO:0003381"}],"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":"apical constriction involved in gastrulation","termid":"GO:0003384"}


id: PBO:0041578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C21orf91 overlapping transcript 1","termid":"PBO:0041578"}


id: PBO:0086765
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; shows sequence similarity to FLO1 and other flocculins","termid":"PBO:0086765"}


id: PBO:0044328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 8","termid":"PBO:0044328"}


id: PBO:0064832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 10","termid":"PBO:0064832"}


id: PBO:0028387
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_methylglyoxal","termid":"PBO:0028387"}


id: PBO:0052533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kallikrein related peptidase 6","termid":"PBO:0052533"}


id: PBO:0031685
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_peroxisome_degradation","termid":"PBO:0031685"}


id: PBO:0109175
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 3111","termid":"PBO:0109175"}


id: MONDO:0002139
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pathological processes in the sigmoid colon region of the large intestine (intestine, large).","definition_xrefs":["MESH:D012810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colonic disorder","termid":"MONDO:0003409"}],"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":"sigmoid disease","secondary_identifiers":["UMLS:C0037072","DOID:1897","MEDGEN:20752"],"termid":"MONDO:0002139","xrefs":{"Monarch":{"xref_id":"0002139"}}}


id: GO:0060411
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of a cardiac septum is generated and organized. A cardiac septum is a partition that separates parts of the heart.","definition_xrefs":["GOC:dph","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"cardiac chamber morphogenesis","termid":"GO:0003206"},{"relation_name":"part_of","term_name":"cardiac septum development","termid":"GO:0003279"}],"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 septum morphogenesis","secondary_identifiers":["GO:0003280"],"synonyms":[{"name":"heart septum morphogenesis","type":"exact"}],"termid":"GO:0060411"}


id: MONDO:0010541
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with increased bone density (obsolete MONDO:0019703)","termid":"MONDO:0019703"},{"relation_name":"is_a","term_name":"hyperostosis","termid":"MONDO:0002185"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked calvarial hyperostosis","secondary_identifiers":["GARD:1058","MESH:C537963","OMIM:302030","Orphanet:391327","MEDGEN:1674665","UMLS:C5190611"],"synonyms":[{"name":"calvarial hyperostosis","type":"related"},{"name":"isolated hyperostosis of the calvarium","type":"related"}],"termid":"MONDO:0010541","xrefs":{"Monarch":{"xref_id":"0010541"}}}


id: PBO:0051534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 4","termid":"PBO:0051534"}


id: GO:0106336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the yolk syncytial layer over time, from its initial formation to the mature structure. The yolk syncytial layer is the peripheral layer of the yolk cell including nuclei and non-yolky cytoplasm.","definition_xrefs":["PMID:29180571"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"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":"yolk syncytial layer development","synonyms":[{"name":"YSL development","type":"related"}],"termid":"GO:0106336"}


id: PBO:0071086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 88","termid":"PBO:0071086"}


id: PBO:0002169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TLDc domain protein 1","termid":"PBO:0002169"}


id: FYPO:0000670
data:
  {"alleles_by_uniquename":{"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03449:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"man1DHEH","gene_uniquename":"SJAG_03449","name":"Man1DHEH","uniquename":"SJAG_03449:allele-2"},"SJAG_03449:allele-3":{"allele_type":"amino_acid_insertion_and_deletion","description":"man1-1-488","gene_uniquename":"SJAG_03449","name":"man1-1-488","uniquename":"SJAG_03449:allele-3"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118820,118818,118819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000671"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid separation is abnormal. Mitotic sister chromatid separation is the process in which sister chromatids are physically detached from each other during mitosis.","definition_xrefs":["PomBase:mah","GO:0051306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"part_of","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03449":null},"genotype_count":3,"genotypes_by_uniquename":{"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Man1DHEH(man1DHEH)","display_uniquename":"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-2","expression":"Not assayed or wild type"}]}]},"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type":{"display_name":"man1-1-488(aa)","display_uniquename":"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-3","expression":"Not assayed or wild type"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000337","FYPO:0005447","FYPO:0000631","FYPO:0000002","FYPO:0001320","FYPO:0000641","FYPO:0001985"],"is_obsolete":false,"name":"abnormal mitotic sister chromatid separation","references_by_uniquename":{"PMID:24184107":null},"single_locus_annotated_genes":["SJAG_03449"],"single_locus_genotype_uniquenames":["man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","man1delta","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal mitotic chromosome separation","type":"exact"},{"name":"abnormal sister chromatid separation during mitosis","type":"exact"},{"name":"abnormal sister chromatid separation during mitotic cell cycle","type":"related"},{"name":"abnormal sister chromatid separation during vegetative growth","type":"exact"},{"name":"aneuploidy","type":"related"},{"name":"mitotic chromosome missegregation","type":"related"}],"termid":"FYPO:0000670","terms_by_termid":{"FYPO:0000671":null}}


id: GO:1990876
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side of the nuclear pore complex (NPC) that faces the cytoplasm.","definition_xrefs":["PMID:8422679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"nuclear pore","termid":"GO:0005643"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005643"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575","GO:0005643"],"is_obsolete":false,"name":"cytoplasmic side of nuclear pore","synonyms":[{"name":"cytoplasmic side of NPC","type":"exact"},{"name":"cytoplasmic side of nuclear pore complex","type":"exact"},{"name":"cytoplasmic side of nucleopore","type":"exact"}],"termid":"GO:1990876"}


id: MONDO:0008928
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cataract-ataxia-deafness syndrome is characterized by mild intellectual deficit, congenital cataract, progressive sensorineural deafness and ataxia. It has been described in two sisters. The inheritance is likely to be autosomal recessive.","definition_xrefs":["Orphanet:1368"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary ataxia","termid":"MONDO:0100309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cataract-ataxia-deafness syndrome","secondary_identifiers":["OMIM:212710","UMLS:C0796123","MEDGEN:163216","GARD:1141","MESH:C538283"],"synonyms":[{"name":"Begeer syndrome","type":"related"},{"name":"cataract ataxia deafness","type":"related"},{"name":"cataract ataxia deafness syndrome","type":"related"},{"name":"cataract-ataxia-deafness-retardation syndrome","type":"related"},{"name":"polyneuropathy, cataract, deafness syndrome","type":"related"},{"name":"polyneuropathy-cataract-deafness syndrome","type":"related"}],"termid":"MONDO:0008928","xrefs":{"Monarch":{"xref_id":"0008928"}}}


id: GO:0099514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of synaptic vesicles along cytoskeletal fibers such as microfilaments or microtubules within a cell, powered by molecular motors.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synaptic vesicle transport","termid":"GO:0048489"},{"relation_name":"is_a","term_name":"vesicle cytoskeletal trafficking","termid":"GO:0099518"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"synaptic vesicle cytoskeletal transport","termid":"GO:0099514"}


id: PBO:0082475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cAMP-dependent protein kinase catalytic subunit; promotes vegetative growth in response to nutrients via the Ras-cAMP signaling pathway; partially redundant with Tpk1p and Tpk3p; localizes to P-bodies during stationary phase; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082475"}


id: MONDO:0003690
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anaplastic ependymoma occurring in adults.","definition_xrefs":["NCIT:C8269"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anaplastic ependymoma","termid":"MONDO:0016700"}],"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":"adult anaplastic ependymoma","secondary_identifiers":["MEDGEN:83709","DOID:5890","UMLS:C0280787"],"synonyms":[{"name":"adult anaplastic ependymoma","type":"exact"},{"name":"adult malignant ependymoma","type":"exact"},{"name":"anaplastic ependymoma","type":"broad"},{"name":"anaplastic ependymoma of adults","type":"exact"},{"name":"malignant adult ependymoma","type":"exact"}],"termid":"MONDO:0003690","xrefs":{"Monarch":{"xref_id":"0003690"}}}


id: PBO:0084111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Heat shock protein that is highly induced upon stress; plays a role in SRP-dependent cotranslational protein-membrane targeting and translocation; member of the HSP70 family; cytoplasmic protein that concentrates in nuclei upon starvation; SSA4 has a paralog, SSA3, that arose from the whole genome duplication","termid":"PBO:0084111"}


id: GO:0035747
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a natural killer cell guided by a specific chemical concentration gradient. Movement may be towards a higher concentration (positive chemotaxis) or towards a lower concentration (negative chemotaxis).","definition_xrefs":["CL:0000623","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphocyte chemotaxis","termid":"GO:0048247"}],"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":"natural killer cell chemotaxis","termid":"GO:0035747"}


id: PBO:0002294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin Kap104","termid":"PBO:0002294"}


id: MONDO:0011203
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"campomelic dysplasia","termid":"MONDO:0007251"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pierre Robin sequence with pectus excavatum and rib and scapular anomalies","secondary_identifiers":["OMIM:602196","MEDGEN:355549","UMLS:C1865783","GARD:10090","MESH:C535775"],"synonyms":[{"name":"Pierre Robin sequence with pectus excavatum and rib and scapular anomalies","type":"exact"},{"name":"campomelic dysplasia, mild","type":"related"},{"name":"skeletal dysplasia related to campomelic dysplasia","type":"related"}],"termid":"MONDO:0011203","xrefs":{"Monarch":{"xref_id":"0011203"}}}


id: GO:0009950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment, maintenance and elaboration of the dorsal/ventral axis. The dorsal/ventral axis is defined by a line that runs orthogonal to both the anterior/posterior and left/right axes. The dorsal end is defined by the upper or back side of an organism. The ventral end is defined by the lower or front side of an organism.","definition_xrefs":["GOC:go_curators","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axis specification","termid":"GO:0009798"},{"relation_name":"part_of","term_name":"dorsal/ventral pattern formation","termid":"GO:0009953"}],"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":"dorsal/ventral axis specification","synonyms":[{"name":"dorsal-ventral axis specification","type":"exact"},{"name":"dorsal/ventral axis determination","type":"related"},{"name":"dorsoventral axis specification","type":"exact"}],"termid":"GO:0009950"}


id: PBO:0036513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH and CC/hC domain splicing factor Bpb1","termid":"PBO:0036513"}


id: PBO:0108898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 11","termid":"PBO:0108898"}


id: PBO:0086026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; undergoes sumoylation; transcription induced under cell wall stress; protein levels are reduced under anaerobic conditions; protein abundance increases in response to DNA replication stress; originally thought to be a mitochondrial ribosomal protein based on sequence analysis","termid":"PBO:0086026"}


id: PR:P36623
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 2,3-bisphosphoglycerate-dependent phosphoglycerate mutase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycerate mutase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26F1.06","secondary_identifiers":["UniProtKB:P36623"],"synonyms":[{"name":"BPG-dependent PGAM (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"MPGM (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PGAM (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Phosphoglyceromutase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC26F1.06","type":"related"},{"name":"Spom972h-gpmA","type":"exact"}],"termid":"PR:P36623"}


id: PBO:0082525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cell death protease essential for hypochlorite-induced apoptosis; involved in the processing of killer toxin and alpha factor precursor; cleaves Lys and Arg residues from the C-terminus of peptides and proteins","termid":"PBO:0082525"}


id: PBO:0028535
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_cell_tip,_with_protein_mislocalized_to_cytoplasm","termid":"PBO:0028535"}


id: MONDO:0030077
data:
  {"annotated_genes":["SJAG_02618"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85047],"is_not":false,"summary":null,"term":"MONDO:0030077"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital vertebral-cardiac-renal anomalies syndrome","termid":"MONDO:0020831"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02618":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0006025"],"is_obsolete":false,"name":"vertebral, cardiac, renal, and limb defects syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618845","UMLS:C5394250","GARD:18510","MEDGEN:1709064"],"synonyms":[{"name":"Congenital Nad Deficiency Disorder 3","type":"exact"},{"name":"VCRL3","type":"exact"},{"name":"VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3","type":"exact"},{"name":"vertebral, cardiac, renal, and limb defects syndrome 3","type":"exact"}],"termid":"MONDO:0030077","terms_by_termid":{"MONDO:0030077":null},"xrefs":{"Monarch":{"xref_id":"0030077"}}}


id: GO:1905424
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of Wnt signaling pathway involved in midbrain dopaminergic neuron differentiation.","definition_xrefs":["GOC:bf","GOC:PARL","GOC:TermGenie","GO_REF:0000058","PMID:17244647"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of Wnt-mediated midbrain dopaminergic neuron differentiation (obsolete GO:1905424)","synonyms":[{"name":"regulation of Wg signaling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of Wg signaling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of Wg signaling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of Wg signaling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of Wg signaling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of Wg signalling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of Wg signalling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of Wg signalling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of Wg signalling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of Wg signalling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of Wingless signaling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of Wingless signaling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of Wingless signaling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of Wingless signaling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of Wingless signaling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of Wingless signalling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of Wingless signalling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of Wingless signalling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of Wingless signalling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of Wingless signalling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of Wnt receptor signaling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of Wnt receptor signaling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of Wnt receptor signaling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of Wnt receptor signaling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of Wnt receptor signaling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of Wnt receptor signalling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of Wnt receptor signalling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of Wnt receptor signalling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of Wnt receptor signalling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of Wnt receptor signalling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of Wnt signaling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of Wnt signaling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of Wnt signaling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of Wnt signaling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of Wnt signaling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of Wnt-activated signaling pathway involved in DA neurogenesis from midbrain floor plate","type":"related"},{"name":"regulation of Wnt-activated signaling pathway involved in mDA neuron differentiation","type":"related"},{"name":"regulation of Wnt-activated signaling pathway involved in midbrain DA neurogenesis","type":"related"},{"name":"regulation of Wnt-activated signaling pathway involved in midbrain dopaminergic neuron differentiation","type":"related"},{"name":"regulation of Wnt-activated signaling pathway involved in midbrain dopaminergic neuron production","type":"related"},{"name":"regulation of Wnt-mediated midbrain DA neuron differentiation","type":"exact"},{"name":"regulation of frizzled signaling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of frizzled signaling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of frizzled signaling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of frizzled signaling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of frizzled signaling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of frizzled signalling pathway involved in DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of frizzled signalling pathway involved in mDA neuron differentiation","type":"exact"},{"name":"regulation of frizzled signalling pathway involved in midbrain DA neurogenesis","type":"exact"},{"name":"regulation of frizzled signalling pathway involved in midbrain dopaminergic neuron differentiation","type":"exact"},{"name":"regulation of frizzled signalling pathway involved in midbrain dopaminergic neuron production","type":"exact"},{"name":"regulation of midbrain dopaminergic neuron differentiation by regulation of Wnt signaling","type":"related"}],"termid":"GO:1905424"}


id: PBO:0012579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphthamide synthetase (predicted)","termid":"PBO:0012579"}


id: GO:0035629
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Addition of a carbohydrate or carbohydrate derivative unit via a nitrogen (N) atom of the N-terminal amino acid of a protein.","definition_xrefs":["GOC:bf","GOC:pr"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal protein amino acid N-linked glycosylation (obsolete GO:0035629)","termid":"GO:0035629"}


id: PBO:0005036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAD synthetase (predicted)","termid":"PBO:0005036"}


id: PBO:0080588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 12","termid":"PBO:0080588"}


id: PBO:0049976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIGD2A pseudogene 1","termid":"PBO:0049976"}


id: GO:0003980
data:
  {"annotated_genes":["SJAG_04571"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[113207],"is_not":false,"summary":null,"term":"GO:0003980"}]},"cv_name":"molecular_function","definition":"Catalysis of the addition of UDP-glucose on to asparagine-linked (N-linked) oligosaccharides of the form Man7-9GlcNAc2 on incorrectly folded glycoproteins.","definition_xrefs":["PMID:10764828","GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04571":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"UDP-glucose:glycoprotein glucosyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:61304","Reactome:R-HSA-548884"],"synonyms":[{"name":"UGGT activity","type":"exact"}],"termid":"GO:0003980","terms_by_termid":{"GO:0003980":null}}


id: GO:1901521
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of aspyridone B.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide biosynthetic process","termid":"GO:0030639"},{"relation_name":"is_a","term_name":"pyridine-containing compound biosynthetic process","termid":"GO:0072525"},{"relation_name":"is_a","term_name":"aspyridone B metabolic process","termid":"GO:1901519"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"aspyridone B biosynthetic process","synonyms":[{"name":"aspyridone B anabolism","type":"exact"},{"name":"aspyridone B biosynthesis","type":"exact"},{"name":"aspyridone B formation","type":"exact"},{"name":"aspyridone B synthesis","type":"exact"}],"termid":"GO:1901521"}


id: PBO:0045258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deoxyribonuclease 2, lysosomal","termid":"PBO:0045258"}


id: PBO:0086751
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; predicted to have a role in cell budding based on computational 'guilt by association' analysis","termid":"PBO:0086751"}


id: MONDO:0015089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal recessive form of complex hereditary spastic paraplegia.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive complex spastic paraplegia (obsolete MONDO:0015089)","secondary_identifiers":["Orphanet:100981"],"synonyms":[{"name":"autosomal recessive complex HSP","type":"exact"},{"name":"autosomal recessive complex SPG","type":"exact"},{"name":"autosomal recessive complex hereditary spastic paraplegia","type":"exact"},{"name":"autosomal recessive complicated HSP","type":"exact"},{"name":"autosomal recessive complicated SPG","type":"exact"},{"name":"autosomal recessive complicated spastic paraplegia","type":"exact"},{"name":"complex hereditary spastic paraplegia, autosomal recessive","type":"exact"}],"termid":"MONDO:0015089","xrefs":{"Monarch":{"xref_id":"0015089"}}}


id: MONDO:0001358
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the bronchus.","definition_xrefs":["MONDO:patterns/location_top"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lower respiratory tract disorder","termid":"MONDO:0000270"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bronchial disorder","secondary_identifiers":["DOID:1176","NCIT:C34439","SCTID:41427001","ICD9:519.19","MESH:D001982","UMLS:C0006261","MEDGEN:14233","EFO:1002018"],"synonyms":[{"name":"bronchial disorder","type":"exact"},{"name":"bronchospasm","type":"exact"},{"name":"bronchus disease","type":"exact"},{"name":"bronchus disease or disorder","type":"exact"},{"name":"disease of bronchus","type":"exact"},{"name":"disease or disorder of bronchus","type":"exact"},{"name":"disorder of bronchus","type":"exact"}],"termid":"MONDO:0001358","xrefs":{"Monarch":{"xref_id":"0001358"}}}


id: PBO:0049829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HDGFL3 pseudogene 1","termid":"PBO:0049829"}


id: PBO:0072839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAP30 like","termid":"PBO:0072839"}


id: PBO:0060825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NECTIN1 divergent transcript","termid":"PBO:0060825"}


id: MONDO:0030977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neuronopathy, distal hereditary motor, autosomal recessive","termid":"MONDO:0015363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005244","MONDO:0005559"],"is_obsolete":false,"name":"neuronopathy, distal hereditary motor, autosomal recessive 7","secondary_identifiers":["DOID:0081426","MEDGEN:1786836","OMIM:619216","UMLS:C5543119","GARD:18444"],"synonyms":[{"name":"HMNMYO","type":"exact"},{"name":"neuropathy, hereditary motor, with myopathic features","type":"exact"}],"termid":"MONDO:0030977","xrefs":{"Monarch":{"xref_id":"0030977"}}}


id: GO:1901840
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of RNA polymerase I regulatory region sequence-specific DNA binding.","definition_xrefs":["GOC:TermGenie","GOC:sart"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of RNA polymerase I regulatory region sequence-specific DNA binding (obsolete GO:1901840)","synonyms":[{"name":"down regulation of RNA polymerase I regulatory region sequence-specific DNA binding","type":"exact"},{"name":"down-regulation of RNA polymerase I regulatory region sequence-specific DNA binding","type":"exact"},{"name":"downregulation of RNA polymerase I regulatory region sequence-specific DNA binding","type":"exact"},{"name":"inhibition of RNA polymerase I regulatory region sequence-specific DNA binding","type":"narrow"}],"termid":"GO:1901840"}


id: MONDO:0003346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Vasculitis affecting the blood vessels of the brain and/or spinal cord.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system disorder","termid":"MONDO:0002602"},{"relation_name":"is_a","term_name":"vasculitis","termid":"MONDO:0018882"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"central nervous system vasculitis","secondary_identifiers":["MEDGEN:148408","MESH:D020293","NCIT:C84622","UMLS:C0751878","DOID:525"],"synonyms":[{"name":"central nervous system vasculitis","type":"exact"},{"name":"vasculitis of central nervous system","type":"exact"}],"termid":"MONDO:0003346","xrefs":{"Monarch":{"xref_id":"0003346"}}}


id: MONDO:0005078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant fibroepithelial neoplasm arising from the breast and rarely the prostate gland. It may recur following resection. The recurrence rates are higher for borderline and malignant phyllodes tumors. In borderline and malignant phyllodes tumors metastases to distant anatomic sites can occur. The incidence of metastases is higher in malignant phyllodes tumors.","definition_xrefs":["NCIT:C2977"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroepithelial neoplasm","termid":"MONDO:0021045"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phyllodes tumor","secondary_identifiers":["EFO:0000653","MEDGEN:1209","MESH:D003557","UMLS:C0010701"],"synonyms":[{"name":"CSP","type":"exact"},{"name":"cystosarcoma phyllodes","type":"exact"},{"name":"phyllodes neoplasm","type":"exact"},{"name":"phyllodes tumor","type":"exact"}],"termid":"MONDO:0005078","xrefs":{"Monarch":{"xref_id":"0005078"}}}


id: MONDO:0021470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the pancreas.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign digestive system neoplasm","termid":"MONDO:0000385"},{"relation_name":"is_a","term_name":"pancreatic neoplasm","termid":"MONDO:0021040"}],"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":"benign neoplasm of pancreas","secondary_identifiers":["NCIT:C4612","UMLS:C0347284","SCTID:92264007","ICD10CM:D13.6","icd11.foundation:1870352651","MEDGEN:91126"],"synonyms":[{"name":"benign neoplasm of the pancreas","type":"exact"},{"name":"benign pancreas neoplasm","type":"exact"},{"name":"benign pancreas tumor","type":"exact"},{"name":"benign pancreas tumour","type":"exact"},{"name":"benign pancreatic neoplasm","type":"exact"},{"name":"benign pancreatic tumor","type":"exact"},{"name":"benign pancreatic tumour","type":"exact"},{"name":"benign tumor of pancreas","type":"exact"},{"name":"benign tumor of the pancreas","type":"exact"},{"name":"benign tumour of pancreas","type":"exact"},{"name":"benign tumour of the pancreas","type":"exact"},{"name":"pancreas benign neoplasm","type":"exact"},{"name":"pancreas neoplasm, benign","type":"exact"},{"name":"pancreas tumor, benign","type":"exact"},{"name":"pancreatic neoplasm, benign","type":"exact"},{"name":"pancreatic tumor, benign","type":"exact"}],"termid":"MONDO:0021470","xrefs":{"Monarch":{"xref_id":"0021470"}}}


id: PBO:0085047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-essential protein involved in pre-mRNA splicing; component of a complex containing Cef1p; has similarity to S. pombe Cwf15p","termid":"PBO:0085047"}


id: FYPO:0008017
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cells grow normally (i.e. indistinguishably from wild type) in a medium containing glutamate as the nitrogen source.","definition_xrefs":["PomBase:mlr","PMID:7903653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0000139","FYPO:0002058","FYPO:0000257","FYPO:0002057","FYPO:0000003"],"is_obsolete":false,"name":"normal growth on glutamate nitrogen source","synonyms":[{"name":"normal cell population growth on glutamate nitrogen source","type":"exact"}],"termid":"FYPO:0008017"}


id: MOD:00933
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative - 5-hydro-5-methylimidazol-4-one, arginine methylglyoxal arginine adduct (+54 amu)","definition_xrefs":["Unimod:319#R"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C3-H2-O adduct (+54 amu) of malondialdehyde with lysine or methylglyoxal with arginine.","termid":"MOD:00630"},{"relation_name":"is_a","term_name":"modified L-arginine residue","termid":"MOD:00902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylglyoxal arginine adduct (+54 amu)","synonyms":[{"name":"Delta:H(2)C(3)O(1)","type":"related"},{"name":"MDA adduct +54","type":"related"}],"termid":"MOD:00933"}


id: GO:0016667
data:
  {"annotated_genes":["SJAG_04060","SJAG_02599","SJAG_03992","SJAG_05027","SJAG_01647","SJAG_01693","SJAG_03653","SJAG_00822","SJAG_02827","SJAG_01417","SJAG_01199","SJAG_01038","SJAG_00419","SJAG_00365","SJAG_03414","SJAG_04953","SJAG_02495","SJAG_00196","SJAG_01292","SJAG_04632","SJAG_04046","SJAG_01162","SJAG_04539","SJAG_03290","SJAG_02016","SJAG_00614","SJAG_02489","SJAG_04399","SJAG_00288","SJAG_00489","SJAG_04125"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[86947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004148"},{"annotations":[117839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015036"},{"annotations":[96639,102672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016971"},{"annotations":[114188,97451,88917,106882,101103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015038"},{"annotations":[104697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004362"},{"annotations":[95069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036456"},{"annotations":[94556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016668"},{"annotations":[106073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033743"},{"annotations":[95070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008113"},{"annotations":[88289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004604"},{"annotations":[106263],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047134"},{"annotations":[102352,99499,110282,101104,110597,114227,88919,90404,97997,116818,91824,88132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015035"},{"annotations":[107897],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070224"},{"annotations":[101297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032542"},{"annotations":[87286,116922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004783"},{"annotations":[114228,110283,97998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016972"},{"annotations":[109549,79005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004791"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a sulfur-containing group acts as a hydrogen or electron donor and reduces a hydrogen or electron acceptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity","termid":"GO:0016491"}],"gene_count":31,"genes_by_uniquename":{"SJAG_00196":null,"SJAG_00288":null,"SJAG_00365":null,"SJAG_00419":null,"SJAG_00489":null,"SJAG_00614":null,"SJAG_00822":null,"SJAG_01038":null,"SJAG_01162":null,"SJAG_01199":null,"SJAG_01292":null,"SJAG_01417":null,"SJAG_01647":null,"SJAG_01693":null,"SJAG_02016":null,"SJAG_02489":null,"SJAG_02495":null,"SJAG_02599":null,"SJAG_02827":null,"SJAG_03290":null,"SJAG_03414":null,"SJAG_03653":null,"SJAG_03992":null,"SJAG_04046":null,"SJAG_04060":null,"SJAG_04125":null,"SJAG_04399":null,"SJAG_04539":null,"SJAG_04632":null,"SJAG_04953":null,"SJAG_05027":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:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"oxidoreductase activity, acting on a sulfur group of donors","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-2213240","EC:1.8.-.-"],"synonyms":[{"name":"oxidoreductase activity, acting on sulfur group of donors, other acceptors","type":"narrow"},{"name":"oxidoreductase activity, acting on sulphur group of donors","type":"exact"}],"termid":"GO:0016667","terms_by_termid":{"GO:0004148":null,"GO:0004362":null,"GO:0004604":null,"GO:0004783":null,"GO:0004791":null,"GO:0008113":null,"GO:0015035":null,"GO:0015036":null,"GO:0015038":null,"GO:0016668":null,"GO:0016971":null,"GO:0016972":null,"GO:0032542":null,"GO:0033743":null,"GO:0036456":null,"GO:0047134":null,"GO:0070224":null}}


id: PBO:0109318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Prp19 complex subunit Cdc5/Cef1","termid":"PBO:0109318"}


id: PR:O59791
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A serine racemase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04202","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine racemase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC320.14","secondary_identifiers":["UniProtKB:O59791"],"synonyms":[{"name":"D-serine ammonia-lyase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"D-serine dehydratase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"L-serine ammonia-lyase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"L-serine dehydratase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SRR","type":"exact"}],"termid":"PR:O59791"}


id: GO:1901343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of vasculature development.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of vasculature development","termid":"GO:1901342"},{"relation_name":"negatively_regulates","term_name":"vasculature development","termid":"GO:0001944"}],"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 vasculature development","synonyms":[{"name":"down regulation of vascular system development","type":"related"},{"name":"down regulation of vasculature development","type":"exact"},{"name":"down-regulation of vascular system development","type":"related"},{"name":"down-regulation of vasculature development","type":"exact"},{"name":"downregulation of vascular system development","type":"related"},{"name":"downregulation of vasculature development","type":"exact"},{"name":"inhibition of vascular system development","type":"related"},{"name":"inhibition of vasculature development","type":"narrow"},{"name":"negative regulation of vascular system development","type":"related"}],"termid":"GO:1901343"}


id: GO:0070728
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to L-leucine, 2-amino-4-methylpentanoic acid.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid binding","termid":"GO:0016597"},{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"}],"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":"L-leucine binding","synonyms":[{"name":"Leu binding","type":"broad"},{"name":"leucine binding","type":"broad"}],"termid":"GO:0070728"}


id: PBO:0072093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S12 pseudogene 24","termid":"PBO:0072093"}


id: PBO:0060554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurobeachin","termid":"PBO:0060554"}


id: PBO:0075297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterol O-acyltransferase 2","termid":"PBO:0075297"}


id: PBO:0044272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X-C motif chemokine ligand 12","termid":"PBO:0044272"}


id: FYPO:0002466
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A mixed population phenotype in which all cells in a population are inviable, and the population includes a mixture of ungerminated spores, germinated spores and cells with abnormal morphology (i.e. size, shape, or structure). The cells with normal morphology arise from division of some of the germinated spores, and may form a microcolony of up to 64 cells.","definition_xrefs":["PomBase:vw","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable mixed population including spores, germinated spores and cells with abnormal morphology (obsolete FYPO:0002466)","termid":"FYPO:0002466"}


id: GO:0140640
data:
  {"annotated_genes":["SJAG_01433","SJAG_02818","SJAG_01173","SJAG_05353","SJAG_04885","SJAG_01832","SJAG_01221","SJAG_03832","SJAG_00956","SJAG_03578","SJAG_01413","SJAG_00898","SJAG_02558","SJAG_04754","SJAG_01522","SJAG_02563","SJAG_04527","SJAG_02521","SJAG_03036","SJAG_00623","SJAG_00863","SJAG_04265","SJAG_04840","SJAG_02374","SJAG_04369","SJAG_02417","SJAG_00400","SJAG_01248","SJAG_00980","SJAG_03665","SJAG_04285","SJAG_02200","SJAG_01431","SJAG_05214","SJAG_01260","SJAG_04907","SJAG_03091","SJAG_03539","SJAG_00253","SJAG_03626","SJAG_02263","SJAG_00683","SJAG_03982","SJAG_03613","SJAG_02527","SJAG_02242","SJAG_01352","SJAG_01644","SJAG_01302","SJAG_03724","SJAG_00174","SJAG_02821","SJAG_03730","SJAG_02373","SJAG_04453","SJAG_00377","SJAG_03755","SJAG_04736","SJAG_01261","SJAG_03356","SJAG_04735","SJAG_01562","SJAG_01938","SJAG_02294","SJAG_00272","SJAG_01410","SJAG_05295","SJAG_04372","SJAG_03734","SJAG_04094","SJAG_05197","SJAG_04519","SJAG_01620","SJAG_01797","SJAG_01551","SJAG_00559","SJAG_02156","SJAG_03132","SJAG_04974","SJAG_03077","SJAG_02382","SJAG_04183","SJAG_05221","SJAG_01119","SJAG_01259","SJAG_00884","SJAG_04084","SJAG_03886","SJAG_02199","SJAG_04181","SJAG_01836","SJAG_05173","SJAG_04689","SJAG_00319","SJAG_04407","SJAG_00857","SJAG_01713","SJAG_01315","SJAG_02084","SJAG_02627","SJAG_05373","SJAG_04772","SJAG_03495","SJAG_04480","SJAG_05334","SJAG_03585","SJAG_02547","SJAG_03898","SJAG_01235","SJAG_00796","SJAG_04877","SJAG_00637","SJAG_04147","SJAG_02182","SJAG_00772","SJAG_00111","SJAG_03876","SJAG_02298","SJAG_02879","SJAG_00583","SJAG_00597","SJAG_05372","SJAG_01269","SJAG_02281","SJAG_00500","SJAG_01463","SJAG_00306","SJAG_02872","SJAG_03277","SJAG_02015","SJAG_03901","SJAG_01653","SJAG_00420","SJAG_02287","SJAG_02817","SJAG_00925","SJAG_00255","SJAG_01958","SJAG_01044","SJAG_02348","SJAG_02686","SJAG_06597","SJAG_01648","SJAG_00198","SJAG_00966","SJAG_05008","SJAG_00081","SJAG_01807","SJAG_00653","SJAG_04824","SJAG_04081","SJAG_01704","SJAG_02540","SJAG_04508","SJAG_03675","SJAG_00729","SJAG_00488","SJAG_02571","SJAG_04034","SJAG_03234","SJAG_02906","SJAG_02993","SJAG_02835","SJAG_00616","SJAG_04993","SJAG_06586","SJAG_00731","SJAG_05249","SJAG_02275","SJAG_03994","SJAG_01499","SJAG_03932","SJAG_02748","SJAG_02610","SJAG_04669","SJAG_02295","SJAG_01152","SJAG_02236","SJAG_03745","SJAG_04791","SJAG_01677","SJAG_04261","SJAG_05313","SJAG_00943","SJAG_00757","SJAG_02386","SJAG_01577","SJAG_03567","SJAG_05193","SJAG_03952","SJAG_00153","SJAG_04435","SJAG_00786","SJAG_04038","SJAG_01262","SJAG_02517","SJAG_01948","SJAG_00871","SJAG_00103","SJAG_03796","SJAG_01476","SJAG_03713","SJAG_04065","SJAG_02721","SJAG_04006","SJAG_04755","SJAG_03206","SJAG_03157","SJAG_05105","SJAG_02460","SJAG_01368","SJAG_01878","SJAG_04355","SJAG_00936","SJAG_03962","SJAG_02101","SJAG_16455","SJAG_05693","SJAG_02653","SJAG_05276","SJAG_00475","SJAG_00325","SJAG_06022","SJAG_03533","SJAG_01354","SJAG_02383","SJAG_00308","SJAG_01822","SJAG_01971","SJAG_00682","SJAG_16460","SJAG_02575","SJAG_04816","SJAG_04488","SJAG_03468","SJAG_04916","SJAG_00619","SJAG_01623","SJAG_02991","SJAG_01163","SJAG_00841","SJAG_02698","SJAG_02506","SJAG_04894","SJAG_04161","SJAG_02267","SJAG_02615","SJAG_04198","SJAG_00722","SJAG_03773","SJAG_03289","SJAG_03780","SJAG_04408","SJAG_04418","SJAG_02790","SJAG_04210","SJAG_03913","SJAG_02556","SJAG_01419","SJAG_04233","SJAG_03367","SJAG_00754","SJAG_00611","SJAG_05025","SJAG_01182","SJAG_03897","SJAG_04114","SJAG_04994","SJAG_00798","SJAG_02528","SJAG_04818","SJAG_04587","SJAG_04019","SJAG_04650","SJAG_03332","SJAG_04409","SJAG_03479","SJAG_00886","SJAG_01010","SJAG_04150","SJAG_02226","SJAG_03877","SJAG_00499","SJAG_00399","SJAG_02187","SJAG_04410","SJAG_02658","SJAG_04089","SJAG_02061","SJAG_02828","SJAG_03689","SJAG_00401","SJAG_04064","SJAG_03554","SJAG_01884","SJAG_02039","SJAG_01575","SJAG_02261","SJAG_05280","SJAG_01041","SJAG_04030","SJAG_00119","SJAG_05239","SJAG_04762","SJAG_00088","SJAG_03240","SJAG_02288","SJAG_01197","SJAG_06642","SJAG_00443","SJAG_02600","SJAG_02690","SJAG_00995","SJAG_00814","SJAG_04091","SJAG_01762","SJAG_03181","SJAG_02070","SJAG_05979","SJAG_00358","SJAG_02822","SJAG_02908","SJAG_03236","SJAG_02977","SJAG_00892","SJAG_02024","SJAG_00997","SJAG_03545","SJAG_04738","SJAG_02370","SJAG_02206","SJAG_03761","SJAG_02428","SJAG_04692","SJAG_04530","SJAG_01444","SJAG_04589","SJAG_04752","SJAG_03035","SJAG_06613","SJAG_03071","SJAG_03425","SJAG_01313","SJAG_04118","SJAG_04934","SJAG_03016","SJAG_02350","SJAG_02031","SJAG_02621","SJAG_04230","SJAG_01765","SJAG_01314","SJAG_04473","SJAG_03014","SJAG_00986","SJAG_02606","SJAG_05257","SJAG_01375","SJAG_05237","SJAG_00806","SJAG_02708","SJAG_02553","SJAG_02545","SJAG_00887","SJAG_05560","SJAG_03923","SJAG_04680","SJAG_02978","SJAG_06284","SJAG_03906","SJAG_03921","SJAG_04153","SJAG_04582","SJAG_05228","SJAG_00243","SJAG_01159","SJAG_03276","SJAG_00955","SJAG_04482","SJAG_01724","SJAG_04856","SJAG_03008","SJAG_03144","SJAG_01953","SJAG_00458","SJAG_02637","SJAG_01798","SJAG_02099","SJAG_02042","SJAG_03328","SJAG_16456","SJAG_03193","SJAG_04106","SJAG_03572","SJAG_03636"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052909"},{"annotations":[91788],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106388"},{"annotations":[94692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052907"},{"annotations":[118202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990599"},{"annotations":[92239,97754,92242,92240,92159,112396,95522,110399,93165,112394,89773,112398,113729,91470,92241,109681,100142,112395,112397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043138"},{"annotations":[105897,114725,106716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033679"},{"annotations":[104330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034458"},{"annotations":[108571,104702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008296"},{"annotations":[91765,98445,104739,95129,101577,115103,103159,107249,110704,107952,89490,103894,102428,116049,106931,114773,117745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000175"},{"annotations":[118373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106334"},{"annotations":[116553],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048257"},{"annotations":[91665,109361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042781"},{"annotations":[118374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017005"},{"annotations":[105413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990043"},{"annotations":[103644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990601"},{"annotations":[96629,87910,92506],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035312"},{"annotations":[111968,91686,117622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043139"},{"annotations":[99382,111969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033678"},{"annotations":[90138,89826,94465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004534"},{"annotations":[99383],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032574"},{"annotations":[95382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051575"},{"annotations":[103645,107224,87911,102682,96630,100665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017108"},{"annotations":[91207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140432"},{"annotations":[95648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034042"},{"annotations":[95649],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034043"},{"annotations":[94372,73653,95650],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034039"},{"annotations":[93223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004813"},{"annotations":[101069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003905"},{"annotations":[94548,97169,104146,112085,115490,93224,97587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002161"},{"annotations":[101559,107607,91082,98156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004045"},{"annotations":[68616],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004812"},{"annotations":[106687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004814"},{"annotations":[104544,101759],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004816"},{"annotations":[117491,113494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004815"},{"annotations":[88414,89717,110698,98571,88151,100044,117032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008094"},{"annotations":[116142,118358,89584,94979,96592,116143,111691,101184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140658"},{"annotations":[105540,115888,91272,100045,92187,88113,98572,100077,104056,96425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140664"},{"annotations":[87500],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140849"},{"annotations":[95952,103050,94118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140665"},{"annotations":[112530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140674"},{"annotations":[111972,106419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061995"},{"annotations":[117366,69835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052929"},{"annotations":[95651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140078"},{"annotations":[89187,95749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061775"},{"annotations":[87387,110006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140670"},{"annotations":[100666,59418,94241,116554,101017,96426],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008821"},{"annotations":[87254,74453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052927"},{"annotations":[105394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043907"},{"annotations":[95075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004817"},{"annotations":[99943],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051500"},{"annotations":[115128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033699"},{"annotations":[106456,88639,93473,95816,112185,91222,112278,89093,111724,94776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003689"},{"annotations":[111725,112279,94777,89094,93474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061860"},{"annotations":[89894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004520"},{"annotations":[101185,111692,76404,88690,96660],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003678"},{"annotations":[113337,92071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003910"},{"annotations":[92072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003909"},{"annotations":[105667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034335"},{"annotations":[89895],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004536"},{"annotations":[94742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034061"},{"annotations":[102442,98915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003896"},{"annotations":[101684,98574,92188,100046,98573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000150"},{"annotations":[103912,104110],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003917"},{"annotations":[105668,89805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003918"},{"annotations":[88810,92754,112831,102664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015616"},{"annotations":[109415,117206],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003906"},{"annotations":[101071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052820"},{"annotations":[74095,101072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008725"},{"annotations":[101073,74093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043916"},{"annotations":[116209,104354,91545,93603,100998,102175,114114,105264,102024,109242,101268,102443,94638,104802,95383,96316,107167,107904,113244,108735,93415,89072,111825,115116,101038,115901],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003899"},{"annotations":[102367,115805,102317,102389,116766,95384,98811,108574,96936,106822,103477,104407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003887"},{"annotations":[88067,109416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008311"},{"annotations":[96632,107225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051908"},{"annotations":[100667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990238"},{"annotations":[89315,78408,117625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036121"},{"annotations":[101665,107954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032296"},{"annotations":[100668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106332"},{"annotations":[117535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070551"},{"annotations":[113876],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008859"},{"annotations":[104333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000384"},{"annotations":[78411],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061749"},{"annotations":[95525,70405,92162,100146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009378"},{"annotations":[111976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160225"},{"annotations":[89837,100950],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004818"},{"annotations":[108756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004819"},{"annotations":[96162,110744,117835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050567"},{"annotations":[96512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004820"},{"annotations":[69692,101992],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004386"},{"annotations":[107834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004821"},{"annotations":[87680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140751"},{"annotations":[112087,115492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004822"},{"annotations":[97589,94550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004823"},{"annotations":[104842,115122],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004824"},{"annotations":[94748,104679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004825"},{"annotations":[90510],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004479"},{"annotations":[89972,93432],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062152"},{"annotations":[116193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004482"},{"annotations":[91209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034353"},{"annotations":[98486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140818"},{"annotations":[107682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004484"},{"annotations":[109222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001734"},{"annotations":[87681,112744,113567,114456,94122,92116],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140750"},{"annotations":[95653],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008534"},{"annotations":[95654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000703"},{"annotations":[98600,100587,101425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000048"},{"annotations":[93134,96713,117479],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004826"},{"annotations":[91210],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990174"},{"annotations":[92912,107250,112367,116050,115108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004535"},{"annotations":[93230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990838"},{"annotations":[106584,105395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004827"},{"annotations":[94375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000701"},{"annotations":[73233,115439,102928,109304,101667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004525"},{"annotations":[104036,114841,105132,118030,112934,94217,104253,105131,114754,96002,98994,96292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000171"},{"annotations":[112935,118031,96293,114755,98995,94218,101546,104037,104254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004526"},{"annotations":[107501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990276"},{"annotations":[95542],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071164"},{"annotations":[88549,115777,106933,87864,89036,90140,95338,112368,108464,89897,117512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004521"},{"annotations":[117537,91723],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016891"},{"annotations":[99120,100532,106934,91766],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004532"},{"annotations":[106747,117272,111457,87263,99726,104754,115062,110224,104005,91879,91900,98459,99121,107263,106578,100901,95762,105246,98839,87295,110423,92201,114264,115811,118109,90127,87043,92792,102240,95622,102617,114870,103020,106387,100129,116675,89317,113026,90313,95504,113297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003724"},{"annotations":[89744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008419"},{"annotations":[90162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003972"},{"annotations":[112138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008173"},{"annotations":[91211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110152"},{"annotations":[104588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110153"},{"annotations":[106935,115109,115152,89898,89829,95569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004540"},{"annotations":[105265,89073,91546,102827,112585,93416,113659,113245,110133,102176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001054"},{"annotations":[102828,93606,113246,93417,91547,96317,107168,114115,105266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001055"},{"annotations":[89074,113247,93418,97655,110929,105267,102829,102177,91548,92531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001056"},{"annotations":[91185,90299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050265"},{"annotations":[99067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003968"},{"annotations":[108587,102434,87820,97623],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004523"},{"annotations":[86938,98363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016433"},{"annotations":[97910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106142"},{"annotations":[59350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000179"},{"annotations":[113058,95122],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009383"},{"annotations":[94406],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070043"},{"annotations":[89142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070039"},{"annotations":[90831],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070037"},{"annotations":[100840,89143,107846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008650"},{"annotations":[115647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070042"},{"annotations":[109661,107561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008649"},{"annotations":[94173,94936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004828"},{"annotations":[105900,106719,108548,114729],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990518"},{"annotations":[106824,88070,100636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008310"},{"annotations":[96634,111039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045145"},{"annotations":[89899,110277,109496,88071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000014"},{"annotations":[103650,111978,91474,114557,109687,94566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017116"},{"annotations":[108579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090486"},{"annotations":[113740,94860,105701],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106032"},{"annotations":[107403,107402],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003720"},{"annotations":[93981,106753],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004829"},{"annotations":[88093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106335"},{"annotations":[100463,111598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160107"},{"annotations":[97351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106340"},{"annotations":[105250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016427"},{"annotations":[106235,109615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052735"},{"annotations":[93433,89973,93434,105251,89974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016428"},{"annotations":[103621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160102"},{"annotations":[106739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160104"},{"annotations":[106740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160103"},{"annotations":[100871],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052906"},{"annotations":[118423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008176"},{"annotations":[98907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052905"},{"annotations":[97577],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030697"},{"annotations":[90453,97352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106050"},{"annotations":[95151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000215"},{"annotations":[97571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102522"},{"annotations":[96531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043399"},{"annotations":[102583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990984"},{"annotations":[96173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052381"},{"annotations":[117243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008193"},{"annotations":[94208,105403,97572],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008175"},{"annotations":[94167,111933,113741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106029"},{"annotations":[105702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160150"},{"annotations":[101985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160148"},{"annotations":[91418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061503"},{"annotations":[87781],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032267"},{"annotations":[117408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141101"},{"annotations":[113264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102521"},{"annotations":[93775],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061708"},{"annotations":[109096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102262"},{"annotations":[109097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102263"},{"annotations":[104171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102264"},{"annotations":[117857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102266"},{"annotations":[117858],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102267"},{"annotations":[88973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102265"},{"annotations":[89192,95299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008479"},{"annotations":[100831,105398,100293,117121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000213"},{"annotations":[105332,93776,107877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0103016"},{"annotations":[95408,96797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004830"},{"annotations":[116842,114483],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004831"},{"annotations":[94693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120048"},{"annotations":[113344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004844"},{"annotations":[104148,97171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004832"}]},"cv_name":"molecular_function","definition":"Catalytic activity that acts to modify a nucleic acid.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity","termid":"GO:0003824"}],"gene_count":395,"genes_by_uniquename":{"SJAG_00081":null,"SJAG_00088":null,"SJAG_00103":null,"SJAG_00111":null,"SJAG_00119":null,"SJAG_00153":null,"SJAG_00174":null,"SJAG_00198":null,"SJAG_00243":null,"SJAG_00253":null,"SJAG_00255":null,"SJAG_00272":null,"SJAG_00306":null,"SJAG_00308":null,"SJAG_00319":null,"SJAG_00325":null,"SJAG_00358":null,"SJAG_00377":null,"SJAG_00399":null,"SJAG_00400":null,"SJAG_00401":null,"SJAG_00420":null,"SJAG_00443":null,"SJAG_00458":null,"SJAG_00475":null,"SJAG_00488":null,"SJAG_00499":null,"SJAG_00500":null,"SJAG_00559":null,"SJAG_00583":null,"SJAG_00597":null,"SJAG_00611":null,"SJAG_00616":null,"SJAG_00619":null,"SJAG_00623":null,"SJAG_00637":null,"SJAG_00653":null,"SJAG_00682":null,"SJAG_00683":null,"SJAG_00722":null,"SJAG_00729":null,"SJAG_00731":null,"SJAG_00754":null,"SJAG_00757":null,"SJAG_00772":null,"SJAG_00786":null,"SJAG_00796":null,"SJAG_00798":null,"SJAG_00806":null,"SJAG_00814":null,"SJAG_00841":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00884":null,"SJAG_00886":null,"SJAG_00887":null,"SJAG_00892":null,"SJAG_00898":null,"SJAG_00925":null,"SJAG_00936":null,"SJAG_00943":null,"SJAG_00955":null,"SJAG_00956":null,"SJAG_00966":null,"SJAG_00980":null,"SJAG_00986":null,"SJAG_00995":null,"SJAG_00997":null,"SJAG_01010":null,"SJAG_01041":null,"SJAG_01044":null,"SJAG_01119":null,"SJAG_01152":null,"SJAG_01159":null,"SJAG_01163":null,"SJAG_01173":null,"SJAG_01182":null,"SJAG_01197":null,"SJAG_01221":null,"SJAG_01235":null,"SJAG_01248":null,"SJAG_01259":null,"SJAG_01260":null,"SJAG_01261":null,"SJAG_01262":null,"SJAG_01269":null,"SJAG_01302":null,"SJAG_01313":null,"SJAG_01314":null,"SJAG_01315":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01368":null,"SJAG_01375":null,"SJAG_01410":null,"SJAG_01413":null,"SJAG_01419":null,"SJAG_01431":null,"SJAG_01433":null,"SJAG_01444":null,"SJAG_01463":null,"SJAG_01476":null,"SJAG_01499":null,"SJAG_01522":null,"SJAG_01551":null,"SJAG_01562":null,"SJAG_01575":null,"SJAG_01577":null,"SJAG_01620":null,"SJAG_01623":null,"SJAG_01644":null,"SJAG_01648":null,"SJAG_01653":null,"SJAG_01677":null,"SJAG_01704":null,"SJAG_01713":null,"SJAG_01724":null,"SJAG_01762":null,"SJAG_01765":null,"SJAG_01797":null,"SJAG_01798":null,"SJAG_01807":null,"SJAG_01822":null,"SJAG_01832":null,"SJAG_01836":null,"SJAG_01878":null,"SJAG_01884":null,"SJAG_01938":null,"SJAG_01948":null,"SJAG_01953":null,"SJAG_01958":null,"SJAG_01971":null,"SJAG_02015":null,"SJAG_02024":null,"SJAG_02031":null,"SJAG_02039":null,"SJAG_02042":null,"SJAG_02061":null,"SJAG_02070":null,"SJAG_02084":null,"SJAG_02099":null,"SJAG_02101":null,"SJAG_02156":null,"SJAG_02182":null,"SJAG_02187":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02206":null,"SJAG_02226":null,"SJAG_02236":null,"SJAG_02242":null,"SJAG_02261":null,"SJAG_02263":null,"SJAG_02267":null,"SJAG_02275":null,"SJAG_02281":null,"SJAG_02287":null,"SJAG_02288":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02298":null,"SJAG_02348":null,"SJAG_02350":null,"SJAG_02370":null,"SJAG_02373":null,"SJAG_02374":null,"SJAG_02382":null,"SJAG_02383":null,"SJAG_02386":null,"SJAG_02417":null,"SJAG_02428":null,"SJAG_02460":null,"SJAG_02506":null,"SJAG_02517":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02528":null,"SJAG_02540":null,"SJAG_02545":null,"SJAG_02547":null,"SJAG_02553":null,"SJAG_02556":null,"SJAG_02558":null,"SJAG_02563":null,"SJAG_02571":null,"SJAG_02575":null,"SJAG_02600":null,"SJAG_02606":null,"SJAG_02610":null,"SJAG_02615":null,"SJAG_02621":null,"SJAG_02627":null,"SJAG_02637":null,"SJAG_02653":null,"SJAG_02658":null,"SJAG_02686":null,"SJAG_02690":null,"SJAG_02698":null,"SJAG_02708":null,"SJAG_02721":null,"SJAG_02748":null,"SJAG_02790":null,"SJAG_02817":null,"SJAG_02818":null,"SJAG_02821":null,"SJAG_02822":null,"SJAG_02828":null,"SJAG_02835":null,"SJAG_02872":null,"SJAG_02879":null,"SJAG_02906":null,"SJAG_02908":null,"SJAG_02977":null,"SJAG_02978":null,"SJAG_02991":null,"SJAG_02993":null,"SJAG_03008":null,"SJAG_03014":null,"SJAG_03016":null,"SJAG_03035":null,"SJAG_03036":null,"SJAG_03071":null,"SJAG_03077":null,"SJAG_03091":null,"SJAG_03132":null,"SJAG_03144":null,"SJAG_03157":null,"SJAG_03181":null,"SJAG_03193":null,"SJAG_03206":null,"SJAG_03234":null,"SJAG_03236":null,"SJAG_03240":null,"SJAG_03276":null,"SJAG_03277":null,"SJAG_03289":null,"SJAG_03328":null,"SJAG_03332":null,"SJAG_03356":null,"SJAG_03367":null,"SJAG_03425":null,"SJAG_03468":null,"SJAG_03479":null,"SJAG_03495":null,"SJAG_03533":null,"SJAG_03539":null,"SJAG_03545":null,"SJAG_03554":null,"SJAG_03567":null,"SJAG_03572":null,"SJAG_03578":null,"SJAG_03585":null,"SJAG_03613":null,"SJAG_03626":null,"SJAG_03636":null,"SJAG_03665":null,"SJAG_03675":null,"SJAG_03689":null,"SJAG_03713":null,"SJAG_03724":null,"SJAG_03730":null,"SJAG_03734":null,"SJAG_03745":null,"SJAG_03755":null,"SJAG_03761":null,"SJAG_03773":null,"SJAG_03780":null,"SJAG_03796":null,"SJAG_03832":null,"SJAG_03876":null,"SJAG_03877":null,"SJAG_03886":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03901":null,"SJAG_03906":null,"SJAG_03913":null,"SJAG_03921":null,"SJAG_03923":null,"SJAG_03932":null,"SJAG_03952":null,"SJAG_03962":null,"SJAG_03982":null,"SJAG_03994":null,"SJAG_04006":null,"SJAG_04019":null,"SJAG_04030":null,"SJAG_04034":null,"SJAG_04038":null,"SJAG_04064":null,"SJAG_04065":null,"SJAG_04081":null,"SJAG_04084":null,"SJAG_04089":null,"SJAG_04091":null,"SJAG_04094":null,"SJAG_04106":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04153":null,"SJAG_04161":null,"SJAG_04181":null,"SJAG_04183":null,"SJAG_04198":null,"SJAG_04210":null,"SJAG_04230":null,"SJAG_04233":null,"SJAG_04261":null,"SJAG_04265":null,"SJAG_04285":null,"SJAG_04355":null,"SJAG_04369":null,"SJAG_04372":null,"SJAG_04407":null,"SJAG_04408":null,"SJAG_04409":null,"SJAG_04410":null,"SJAG_04418":null,"SJAG_04435":null,"SJAG_04453":null,"SJAG_04473":null,"SJAG_04480":null,"SJAG_04482":null,"SJAG_04488":null,"SJAG_04508":null,"SJAG_04519":null,"SJAG_04527":null,"SJAG_04530":null,"SJAG_04582":null,"SJAG_04587":null,"SJAG_04589":null,"SJAG_04650":null,"SJAG_04669":null,"SJAG_04680":null,"SJAG_04689":null,"SJAG_04692":null,"SJAG_04735":null,"SJAG_04736":null,"SJAG_04738":null,"SJAG_04752":null,"SJAG_04754":null,"SJAG_04755":null,"SJAG_04762":null,"SJAG_04772":null,"SJAG_04791":null,"SJAG_04816":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_04840":null,"SJAG_04856":null,"SJAG_04877":null,"SJAG_04885":null,"SJAG_04894":null,"SJAG_04907":null,"SJAG_04916":null,"SJAG_04934":null,"SJAG_04974":null,"SJAG_04993":null,"SJAG_04994":null,"SJAG_05008":null,"SJAG_05025":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05193":null,"SJAG_05197":null,"SJAG_05214":null,"SJAG_05221":null,"SJAG_05228":null,"SJAG_05237":null,"SJAG_05239":null,"SJAG_05249":null,"SJAG_05257":null,"SJAG_05276":null,"SJAG_05280":null,"SJAG_05295":null,"SJAG_05313":null,"SJAG_05334":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_05560":null,"SJAG_05693":null,"SJAG_05979":null,"SJAG_06022":null,"SJAG_06284":null,"SJAG_06586":null,"SJAG_06597":null,"SJAG_06613":null,"SJAG_06642":null,"SJAG_16455":null,"SJAG_16456":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674"],"is_obsolete":false,"name":"catalytic activity, acting on a nucleic acid","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0140640","terms_by_termid":{"GO:0000014":null,"GO:0000048":null,"GO:0000150":null,"GO:0000171":null,"GO:0000175":null,"GO:0000179":null,"GO:0000213":null,"GO:0000215":null,"GO:0000384":null,"GO:0000701":null,"GO:0000703":null,"GO:0001054":null,"GO:0001055":null,"GO:0001056":null,"GO:0001734":null,"GO:0002161":null,"GO:0003678":null,"GO:0003689":null,"GO:0003720":null,"GO:0003724":null,"GO:0003887":null,"GO:0003896":null,"GO:0003899":null,"GO:0003905":null,"GO:0003906":null,"GO:0003909":null,"GO:0003910":null,"GO:0003917":null,"GO:0003918":null,"GO:0003968":null,"GO:0003972":null,"GO:0004045":null,"GO:0004386":null,"GO:0004479":null,"GO:0004482":null,"GO:0004484":null,"GO:0004520":null,"GO:0004521":null,"GO:0004523":null,"GO:0004525":null,"GO:0004526":null,"GO:0004532":null,"GO:0004534":null,"GO:0004535":null,"GO:0004536":null,"GO:0004540":null,"GO:0004812":null,"GO:0004813":null,"GO:0004814":null,"GO:0004815":null,"GO:0004816":null,"GO:0004817":null,"GO:0004818":null,"GO:0004819":null,"GO:0004820":null,"GO:0004821":null,"GO:0004822":null,"GO:0004823":null,"GO:0004824":null,"GO:0004825":null,"GO:0004826":null,"GO:0004827":null,"GO:0004828":null,"GO:0004829":null,"GO:0004830":null,"GO:0004831":null,"GO:0004832":null,"GO:0004844":null,"GO:0008094":null,"GO:0008173":null,"GO:0008175":null,"GO:0008176":null,"GO:0008193":null,"GO:0008296":null,"GO:0008310":null,"GO:0008311":null,"GO:0008419":null,"GO:0008479":null,"GO:0008534":null,"GO:0008649":null,"GO:0008650":null,"GO:0008725":null,"GO:0008821":null,"GO:0008859":null,"GO:0009378":null,"GO:0009383":null,"GO:0015616":null,"GO:0016427":null,"GO:0016428":null,"GO:0016433":null,"GO:0016891":null,"GO:0017005":null,"GO:0017108":null,"GO:0017116":null,"GO:0030697":null,"GO:0032267":null,"GO:0032296":null,"GO:0032574":null,"GO:0033678":null,"GO:0033679":null,"GO:0033699":null,"GO:0034039":null,"GO:0034042":null,"GO:0034043":null,"GO:0034061":null,"GO:0034335":null,"GO:0034353":null,"GO:0034458":null,"GO:0035312":null,"GO:0036121":null,"GO:0042781":null,"GO:0043138":null,"GO:0043139":null,"GO:0043399":null,"GO:0043907":null,"GO:0043916":null,"GO:0045145":null,"GO:0048257":null,"GO:0050265":null,"GO:0050567":null,"GO:0051500":null,"GO:0051575":null,"GO:0051908":null,"GO:0052381":null,"GO:0052735":null,"GO:0052820":null,"GO:0052905":null,"GO:0052906":null,"GO:0052907":null,"GO:0052909":null,"GO:0052927":null,"GO:0052929":null,"GO:0061503":null,"GO:0061708":null,"GO:0061749":null,"GO:0061775":null,"GO:0061860":null,"GO:0061995":null,"GO:0062152":null,"GO:0070037":null,"GO:0070039":null,"GO:0070042":null,"GO:0070043":null,"GO:0070551":null,"GO:0071164":null,"GO:0090486":null,"GO:0102262":null,"GO:0102263":null,"GO:0102264":null,"GO:0102265":null,"GO:0102266":null,"GO:0102267":null,"GO:0102521":null,"GO:0102522":null,"GO:0103016":null,"GO:0106029":null,"GO:0106032":null,"GO:0106050":null,"GO:0106142":null,"GO:0106332":null,"GO:0106334":null,"GO:0106335":null,"GO:0106340":null,"GO:0106388":null,"GO:0110152":null,"GO:0110153":null,"GO:0120048":null,"GO:0140078":null,"GO:0140432":null,"GO:0140658":null,"GO:0140664":null,"GO:0140665":null,"GO:0140670":null,"GO:0140674":null,"GO:0140750":null,"GO:0140751":null,"GO:0140818":null,"GO:0140849":null,"GO:0141101":null,"GO:0160102":null,"GO:0160103":null,"GO:0160104":null,"GO:0160107":null,"GO:0160148":null,"GO:0160150":null,"GO:0160225":null,"GO:1990043":null,"GO:1990174":null,"GO:1990238":null,"GO:1990276":null,"GO:1990518":null,"GO:1990599":null,"GO:1990601":null,"GO:1990838":null,"GO:1990984":null}}


id: GO:0002243
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a stimulus from a parasitic plant is received and converted into a molecular signal.","definition_xrefs":["GOC:add","PMID:16547862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to parasitic plant","termid":"GO:0002241"},{"relation_name":"is_a","term_name":"detection of symbiont","termid":"GO:0009602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of parasitic plant","termid":"GO:0002243"}


id: GO:0046305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of alkanesulfonates, the anion of alkanesulfonic acids, sulfonic acid derivatives containing an aliphatic hydrocarbon group.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic acid biosynthetic process","termid":"GO:0016053"},{"relation_name":"is_a","term_name":"alkanesulfonate metabolic process","termid":"GO:0019694"},{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006790"],"is_obsolete":false,"name":"alkanesulfonate biosynthetic process","synonyms":[{"name":"alkanesulfonate anabolism","type":"exact"},{"name":"alkanesulfonate biosynthesis","type":"exact"},{"name":"alkanesulfonate formation","type":"exact"},{"name":"alkanesulfonate synthesis","type":"exact"},{"name":"alkanesulphonate biosynthesis","type":"exact"},{"name":"alkanesulphonate biosynthetic process","type":"exact"}],"termid":"GO:0046305"}


id: PBO:0046256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongator acetyltransferase complex subunit 5","termid":"PBO:0046256"}


id: PBO:0091765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mating type M-specific polypeptide Mi at silenced MAT3 locus","termid":"PBO:0091765"}


id: GO:0002266
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change in the morphology or behavior of a follicular dendritic cell resulting from exposure to an activating factor such as a cellular or soluble ligand.","definition_xrefs":["GOC:add","PMID:15606789"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell activation","termid":"GO:0001775"}],"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":"follicular dendritic cell activation","termid":"GO:0002266"}


id: GO:0102123
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A4 + O2 + H+ + NAD(P)H = 16alpha,17-epoxy gibberellin A4 + H2O + NAD(P).","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A4 16alpha,17 epoxidase activity (obsolete GO:0102123)","termid":"GO:0102123"}


id: MONDO:0054862
data:
  {"annotated_genes":["SJAG_02294","SJAG_02690"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85943,85944],"is_not":false,"summary":null,"term":"MONDO:0054862"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bone marrow disorder","termid":"MONDO:0003225"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02294":null,"SJAG_02690":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005047"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005047","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"premature ovarian failure 15","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080872","MEDGEN:1648369","OMIM:618096","UMLS:C4748170"],"synonyms":[{"name":"POF15","type":"related"},{"name":"premature ovarian failure 15","type":"exact"}],"termid":"MONDO:0054862","terms_by_termid":{"MONDO:0054862":null},"xrefs":{"Monarch":{"xref_id":"0054862"}}}


