# terms

id: GO:0060187
data:
  {"annotated_genes":["SJAG_01660","SJAG_00185","SJAG_04609","SJAG_00397","SJAG_02486","SJAG_04620","SJAG_01167","SJAG_00236","SJAG_03748","SJAG_02258","SJAG_03643","SJAG_02797","SJAG_04462","SJAG_03453","SJAG_04703","SJAG_04479","SJAG_04322","SJAG_02684","SJAG_02412","SJAG_00596","SJAG_00331","SJAG_01350","SJAG_02004","SJAG_00101","SJAG_04044","SJAG_03331","SJAG_03380","SJAG_03379","SJAG_02087","SJAG_02511","SJAG_05001","SJAG_02368","SJAG_01290","SJAG_01964","SJAG_01787","SJAG_03246","SJAG_00521","SJAG_04901","SJAG_04690","SJAG_02152","SJAG_01095","SJAG_04595","SJAG_01345","SJAG_01718","SJAG_02045","SJAG_03760","SJAG_02320","SJAG_02379","SJAG_03126","SJAG_01631","SJAG_04724","SJAG_00652","SJAG_00610","SJAG_01215","SJAG_04982","SJAG_03581","SJAG_00445","SJAG_04878","SJAG_03119","SJAG_03915","SJAG_03229","SJAG_01770","SJAG_03486","SJAG_01384","SJAG_01388","SJAG_01448","SJAG_02241","SJAG_01855","SJAG_04771","SJAG_00018","SJAG_03357","SJAG_02700","SJAG_02716","SJAG_01196","SJAG_04723","SJAG_00805","SJAG_02075","SJAG_03086","SJAG_00137","SJAG_03011","SJAG_00587","SJAG_04765","SJAG_00317","SJAG_01268","SJAG_00104","SJAG_02695","SJAG_03625","SJAG_01437","SJAG_02392","SJAG_00724","SJAG_04315","SJAG_03637","SJAG_02380","SJAG_04787","SJAG_04781","SJAG_00280","SJAG_00845","SJAG_00264","SJAG_01114","SJAG_01925","SJAG_00216","SJAG_01697","SJAG_01373","SJAG_02333","SJAG_01983","SJAG_04931","SJAG_02916","SJAG_04051","SJAG_02989","SJAG_02278","SJAG_01943","SJAG_02169","SJAG_04706","SJAG_02322","SJAG_02943","SJAG_04258","SJAG_03608","SJAG_00140","SJAG_04668","SJAG_04566","SJAG_03646","SJAG_01885","SJAG_00514","SJAG_02228","SJAG_01754","SJAG_03536","SJAG_02222","SJAG_00870","SJAG_03655","SJAG_02718","SJAG_00800","SJAG_01017","SJAG_00162","SJAG_03746","SJAG_04591","SJAG_04058","SJAG_04522","SJAG_00333","SJAG_01453","SJAG_00661","SJAG_02838","SJAG_01894","SJAG_02924","SJAG_00028","SJAG_04637","SJAG_03025","SJAG_00268","SJAG_00279","SJAG_02968","SJAG_03432","SJAG_01993","SJAG_04167","SJAG_04673","SJAG_00030","SJAG_04776","SJAG_02576","SJAG_01118","SJAG_03375","SJAG_00063","SJAG_04358","SJAG_02602","SJAG_01189","SJAG_02729","SJAG_00424","SJAG_02277","SJAG_05198","SJAG_02957","SJAG_04666","SJAG_00773","SJAG_04001","SJAG_00851","SJAG_04905","SJAG_01799","SJAG_02132","SJAG_03938","SJAG_02202","SJAG_04828","SJAG_04935","SJAG_03753","SJAG_02572","SJAG_00546","SJAG_02760","SJAG_01360","SJAG_02753","SJAG_01003","SJAG_02351","SJAG_01288","SJAG_05264","SJAG_04980","SJAG_02331","SJAG_02062","SJAG_00434","SJAG_03444","SJAG_01978","SJAG_01794","SJAG_04509","SJAG_00152","SJAG_04960","SJAG_00700","SJAG_01888","SJAG_00589","SJAG_05290","SJAG_04624","SJAG_02166","SJAG_00677","SJAG_01071","SJAG_04050","SJAG_04268","SJAG_03754","SJAG_01456","SJAG_03353","SJAG_03596","SJAG_04455","SJAG_02104","SJAG_00993","SJAG_02566","SJAG_02657","SJAG_00368","SJAG_00667","SJAG_01898","SJAG_04100","SJAG_04829","SJAG_02581","SJAG_01353","SJAG_03705","SJAG_00938","SJAG_00575","SJAG_02114","SJAG_04887","SJAG_02338","SJAG_01171","SJAG_05179","SJAG_05285","SJAG_04012","SJAG_01835","SJAG_03606","SJAG_01738","SJAG_03145","SJAG_01732","SJAG_03172"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104534,105590,113319,89314,97223,93738,113613,105385,102055,101777,108937,110273,114264,98730,98169,101617,108961,92896,97701,104554,115041,95398,105145,99593,113824,100707,116010,89330,105642,91152,112051,92662,101191,100852,89960,98839,90275,92587,97062,108777,93206,98131,89863,95700,97269,104864,106556,112814],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051285"},{"annotations":[120640,92537,108021,117788,118460,115010,92566,91676,89685,71796,120838,118150,94248,113907,116127,119890,96424,112707],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902716"},{"annotations":[102815,112708,113908,119891],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140472"},{"annotations":[100694,92299,93307,108616,90769,118061,89798,101559,92305,120336,110232,120534,115743,106899,120883,90067,92304,94107,102840,92302,106436,107094,98895,111319,106639,97557,58656,94169,104741,114966,113431,101466,113455,103367,96243,90433,104119,105425,93428,110305,115631,107536,113388,111473,100784,116144,119493,120756,120796,92301,120985,121230,102085,94871,113330,100102,92303,92988,96852,113635,92032,114436,90108,115801,117624,121313,89259,119716,91431,111465,95491,94098,120874,121231,92787,107261,108410,92298,99424,65790,103245,93943,106528,108198,91646,91527,109152,109995,92300,112117,109111,94377,96229,92306,90049,95573,96804,97110,102276,102808,101163,103644,111279,115415,115634,120337,115179,118716,105209,107079,118817,104638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051286"},{"annotations":[108515],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0106186"},{"annotations":[114127,121295,105775,95718,121299,97274,121301,77224,96795,90279,121303,101639,121297,121305,102058,118547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035838"},{"annotations":[121296,121300,121302,121304,121298,121306],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001411"},{"annotations":[90088,121627,103837,94351,92668,101429,95861,95665,116601,97227,113275,118155,110065,110004,90913,102033,103838],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990819"},{"annotations":[92496,79560,94424,99788,108027,77335,80497,73935,99594,105150,98736,108786,100769,75707,109088,111002,71880,78084,89694,110792,92542,117795,116298],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043332"},{"annotations":[98237,112145],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070867"},{"annotations":[117797,116357,98740,114744,93420,112714,101197,91254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035841"},{"annotations":[90575,106561,92969,116019,111370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035839"},{"annotations":[112716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035842"},{"annotations":[98741,93421,91256,104965,116358,114746,106562,101198,90576,109540,108028,116020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035840"},{"annotations":[98915,89952,112818,110384,117450,114311,89697,103682,116360,95316,94550,90090,91686,94331,94238,111387,117798,119201,102566,98867,97385,104911],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031520"},{"annotations":[79835],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902929"}]},"cv_name":"cellular_component","definition":"Either of two different areas at opposite ends of an axis of a cell.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":240,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00028":null,"SJAG_00030":null,"SJAG_00063":null,"SJAG_00101":null,"SJAG_00104":null,"SJAG_00137":null,"SJAG_00140":null,"SJAG_00152":null,"SJAG_00162":null,"SJAG_00185":null,"SJAG_00216":null,"SJAG_00236":null,"SJAG_00264":null,"SJAG_00268":null,"SJAG_00279":null,"SJAG_00280":null,"SJAG_00317":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00368":null,"SJAG_00397":null,"SJAG_00424":null,"SJAG_00434":null,"SJAG_00445":null,"SJAG_00514":null,"SJAG_00521":null,"SJAG_00546":null,"SJAG_00575":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00596":null,"SJAG_00610":null,"SJAG_00652":null,"SJAG_00661":null,"SJAG_00667":null,"SJAG_00677":null,"SJAG_00700":null,"SJAG_00724":null,"SJAG_00773":null,"SJAG_00800":null,"SJAG_00805":null,"SJAG_00845":null,"SJAG_00851":null,"SJAG_00870":null,"SJAG_00938":null,"SJAG_00993":null,"SJAG_01003":null,"SJAG_01017":null,"SJAG_01071":null,"SJAG_01095":null,"SJAG_01114":null,"SJAG_01118":null,"SJAG_01167":null,"SJAG_01171":null,"SJAG_01189":null,"SJAG_01196":null,"SJAG_01215":null,"SJAG_01268":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01345":null,"SJAG_01350":null,"SJAG_01353":null,"SJAG_01360":null,"SJAG_01373":null,"SJAG_01384":null,"SJAG_01388":null,"SJAG_01437":null,"SJAG_01448":null,"SJAG_01453":null,"SJAG_01456":null,"SJAG_01631":null,"SJAG_01660":null,"SJAG_01697":null,"SJAG_01718":null,"SJAG_01732":null,"SJAG_01738":null,"SJAG_01754":null,"SJAG_01770":null,"SJAG_01787":null,"SJAG_01794":null,"SJAG_01799":null,"SJAG_01835":null,"SJAG_01855":null,"SJAG_01885":null,"SJAG_01888":null,"SJAG_01894":null,"SJAG_01898":null,"SJAG_01925":null,"SJAG_01943":null,"SJAG_01964":null,"SJAG_01978":null,"SJAG_01983":null,"SJAG_01993":null,"SJAG_02004":null,"SJAG_02045":null,"SJAG_02062":null,"SJAG_02075":null,"SJAG_02087":null,"SJAG_02104":null,"SJAG_02114":null,"SJAG_02132":null,"SJAG_02152":null,"SJAG_02166":null,"SJAG_02169":null,"SJAG_02202":null,"SJAG_02222":null,"SJAG_02228":null,"SJAG_02241":null,"SJAG_02258":null,"SJAG_02277":null,"SJAG_02278":null,"SJAG_02320":null,"SJAG_02322":null,"SJAG_02331":null,"SJAG_02333":null,"SJAG_02338":null,"SJAG_02351":null,"SJAG_02368":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02392":null,"SJAG_02412":null,"SJAG_02486":null,"SJAG_02511":null,"SJAG_02566":null,"SJAG_02572":null,"SJAG_02576":null,"SJAG_02581":null,"SJAG_02602":null,"SJAG_02657":null,"SJAG_02684":null,"SJAG_02695":null,"SJAG_02700":null,"SJAG_02716":null,"SJAG_02718":null,"SJAG_02729":null,"SJAG_02753":null,"SJAG_02760":null,"SJAG_02797":null,"SJAG_02838":null,"SJAG_02916":null,"SJAG_02924":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_02968":null,"SJAG_02989":null,"SJAG_03011":null,"SJAG_03025":null,"SJAG_03086":null,"SJAG_03119":null,"SJAG_03126":null,"SJAG_03145":null,"SJAG_03172":null,"SJAG_03229":null,"SJAG_03246":null,"SJAG_03331":null,"SJAG_03353":null,"SJAG_03357":null,"SJAG_03375":null,"SJAG_03379":null,"SJAG_03380":null,"SJAG_03432":null,"SJAG_03444":null,"SJAG_03453":null,"SJAG_03486":null,"SJAG_03536":null,"SJAG_03581":null,"SJAG_03596":null,"SJAG_03606":null,"SJAG_03608":null,"SJAG_03625":null,"SJAG_03637":null,"SJAG_03643":null,"SJAG_03646":null,"SJAG_03655":null,"SJAG_03705":null,"SJAG_03746":null,"SJAG_03748":null,"SJAG_03753":null,"SJAG_03754":null,"SJAG_03760":null,"SJAG_03915":null,"SJAG_03938":null,"SJAG_04001":null,"SJAG_04012":null,"SJAG_04044":null,"SJAG_04050":null,"SJAG_04051":null,"SJAG_04058":null,"SJAG_04100":null,"SJAG_04167":null,"SJAG_04258":null,"SJAG_04268":null,"SJAG_04315":null,"SJAG_04322":null,"SJAG_04358":null,"SJAG_04455":null,"SJAG_04462":null,"SJAG_04479":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04566":null,"SJAG_04591":null,"SJAG_04595":null,"SJAG_04609":null,"SJAG_04620":null,"SJAG_04624":null,"SJAG_04637":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04673":null,"SJAG_04690":null,"SJAG_04703":null,"SJAG_04706":null,"SJAG_04723":null,"SJAG_04724":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04776":null,"SJAG_04781":null,"SJAG_04787":null,"SJAG_04828":null,"SJAG_04829":null,"SJAG_04878":null,"SJAG_04887":null,"SJAG_04901":null,"SJAG_04905":null,"SJAG_04931":null,"SJAG_04935":null,"SJAG_04960":null,"SJAG_04980":null,"SJAG_04982":null,"SJAG_05001":null,"SJAG_05179":null,"SJAG_05198":null,"SJAG_05264":null,"SJAG_05285":null,"SJAG_05290":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"cell pole","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:25866389":null,"PMID:30726171":null,"PMID:36148799":null},"termid":"GO:0060187","terms_by_termid":{"GO:0001411":null,"GO:0031520":null,"GO:0035838":null,"GO:0035839":null,"GO:0035840":null,"GO:0035841":null,"GO:0035842":null,"GO:0043332":null,"GO:0051285":null,"GO:0051286":null,"GO:0051329":null,"GO:0070867":null,"GO:0106186":null,"GO:0140472":null,"GO:1902716":null,"GO:1902929":null,"GO:1990819":null}}


id: MOD:00389
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-proline residue to N-formyl-L-proline.","definition_xrefs":["PubMed:12051774","PubMed:5464655","RESID:AA0384","Unimod:122#N-term"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-formylated residue","termid":"MOD:00409"},{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"},{"relation_name":"is_a","term_name":"alpha-amino acylated residue","termid":"MOD:01696"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-formyl-L-proline","synonyms":[{"name":"(2S)-1-formylpyrrolidine-2-carboxylic acid","type":"exact"},{"name":"1-formyl-2-pyrrolidinecarboxylic acid","type":"exact"},{"name":"1-formylproline","type":"exact"},{"name":"N-formyl-L-proline","type":"exact"},{"name":"N-formylated L-proline","type":"exact"},{"name":"NFoPro","type":"exact"}],"termid":"MOD:00389"}


id: PBO:0089294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPOTS complex subunit, serine palmitoyltransferase activator Tsc3","termid":"PBO:0089294"}


id: MONDO:0003068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the postauricular lymph nodes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphadenitis","termid":"MONDO:0002052"}],"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":"postauricular lymphadenitis","secondary_identifiers":["DOID:4638","NCIT:C27332","MEDGEN:183076","UMLS:C0919638"],"synonyms":[{"name":"lymphadenitis (disease) of mastoid lymph node","type":"exact"},{"name":"mastoid lymph node lymphadenitis (disease)","type":"exact"}],"termid":"MONDO:0003068","xrefs":{"Monarch":{"xref_id":"0003068"}}}


id: PBO:0083574
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 verified ORF YHR073W; identified by expression profiling and mass spectrometry","termid":"PBO:0083574"}


id: PBO:0062762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily P member 2 pseudogene","termid":"PBO:0062762"}


id: MONDO:0011709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Split-hand/foot malformation mapped to chromosome 2q31.","definition_xrefs":["NCIT:C75002"],"direct_ancestors":[{"relation_name":"is_a","term_name":"split hand-foot malformation","termid":"MONDO:0016576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"split hand-foot malformation 5","secondary_identifiers":["GARD:15398","MEDGEN:338277","DOID:0090022","MESH:C564674","OMIM:606708","UMLS:C1847622"],"synonyms":[{"name":"SHFM5","type":"exact"},{"name":"split hand-foot malformation type 5","type":"exact"},{"name":"split-hand/foot malformation 5","type":"related"},{"name":"split-hand/foot malformation type 5","type":"exact"}],"termid":"MONDO:0011709","xrefs":{"Monarch":{"xref_id":"0011709"}}}


id: MONDO:0019401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Steroid-resistant, sporadic idiopathic nephrotic syndrome, is a heterogeneous entity. Nephrotic syndrome is characterized by marked proteinuria, with reduced plasmatic levels of albumin, and potentially with edema.","definition_xrefs":["Orphanet:84271"],"direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic nephrotic syndrome","termid":"MONDO:0018170"},{"relation_name":"is_a","term_name":"steroid-resistant nephrotic syndrome","termid":"MONDO:0044765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"sporadic idiopathic steroid-resistant nephrotic syndrome","secondary_identifiers":["SCTID:717191005","UMLS:C4274017","MEDGEN:897207"],"synonyms":[{"name":"sporadic idiopathic nephrosis","type":"exact"}],"termid":"MONDO:0019401","xrefs":{"Monarch":{"xref_id":"0019401"}}}


id: MONDO:0032904
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Meesmann corneal dystrophy","termid":"MONDO:0007379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"corneal dystrophy, Meesmann, 2","secondary_identifiers":["MEDGEN:1684798","OMIM:618767","DOID:0080671","UMLS:C5231495"],"synonyms":[{"name":"CORNEAL DYSTROPHY, MEESMANN, 2","type":"related"},{"name":"MECD2","type":"related"},{"name":"meesmann corneal dystrophy 2","type":"exact"}],"termid":"MONDO:0032904","xrefs":{"Monarch":{"xref_id":"0032904"}}}


id: PBO:0029963
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_hydrogen_ion_transporting_ATP_synthase_activity,_rotational_mechanism","termid":"PBO:0029963"}


id: GO:0000047
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 Rieske iron-sulfur protein (obsolete GO:0000047)","synonyms":[{"name":"Rieske iron-sulfur protein","type":"exact"},{"name":"Rieske iron-sulphur protein","type":"exact"}],"termid":"GO:0000047"}


id: PBO:0079193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis specific protein Y-linked 22, pseudogene","termid":"PBO:0079193"}


id: MONDO:0009663
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":"mucus inspissation of respiratory tract","secondary_identifiers":["UMLS:C1854729","MEDGEN:340702","MESH:C565366","OMIM:253240"],"synonyms":[{"name":"mucus inspissation of respiratory tract","type":"exact"}],"termid":"MONDO:0009663","xrefs":{"Monarch":{"xref_id":"0009663"}}}


id: PBO:0048816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 5","termid":"PBO:0048816"}


id: MONDO:0000554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma that arises from the endocervix. It is the most common type of endocervical adenocarcinoma. The neoplastic epithelium shows a pseudostratified architecture and the malignant cells have enlarged, elongated, and hyperchromatic nuclei.","definition_xrefs":["NCIT:C127907"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocervical carcinoma","termid":"MONDO:0004259"},{"relation_name":"is_a","term_name":"cervical adenocarcinoma","termid":"MONDO:0005153"}],"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":"endocervical adenocarcinoma","secondary_identifiers":["UMLS:C1263762","DOID:0050940","MEDGEN:688039","SCTID:123842006","ONCOTREE:ECAD"],"synonyms":[{"name":"endocervical adenocarcinoma, usual type","type":"exact"},{"name":"endocervix adenocarcinoma","type":"exact"}],"termid":"MONDO:0000554","xrefs":{"Monarch":{"xref_id":"0000554"}}}


id: PBO:0069492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 759, pseudogene","termid":"PBO:0069492"}


id: PBO:0091715
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human PSMC1","termid":"PBO:0091715"}


id: PR:O94536
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ucp12 gene.","definition_xrefs":["UniProtKB:O94536","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":"ATP-dependent RNA helicase ucp12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC895.09c","synonyms":[{"name":"Spom972h-ucp12","type":"exact"}],"termid":"PR:O94536"}


id: MONDO:0011412
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurodegenerative disease that is characterized by intraneuronal inclusions of mutant neuroserpin resulting in progressive encephalopathy, dementia and seizures and has material basis in a mutation in the SERPINI1 gene inherited in an in autosomal dominant pattern.","definition_xrefs":["DOID:0050831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive myoclonus epilepsy","termid":"MONDO:0020074"},{"relation_name":"is_a","term_name":"Mendelian encephalopathy","termid":"MONDO:0100198"}],"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":"familial encephalopathy with neuroserpin inclusion bodies","secondary_identifiers":["Orphanet:85110","SCTID:702421006","MEDGEN:346965","ICD9:348.39","NORD:1123","UMLS:C1858680","icd11.foundation:453919434","GARD:10037","MESH:C536841","OMIM:604218"],"synonyms":[{"name":"FENIB","type":"exact"},{"name":"encephalopathy, familial, with Collins bodies","type":"related"},{"name":"encephalopathy, familial, with neuroserpin inclusion bodies","type":"related"}],"termid":"MONDO:0011412","xrefs":{"Monarch":{"xref_id":"0011412"}}}


id: PBO:0054483
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 1883","termid":"PBO:0054483"}


id: GO:0006126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete other pathways of electron transport (obsolete GO:0006126)","synonyms":[{"name":"other pathways of electron transport","type":"exact"}],"termid":"GO:0006126"}


id: PBO:0073495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small G protein signaling modulator 1","termid":"PBO:0073495"}


id: MONDO:0004893
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Vertical strabismus in which there is permanent upward deviation of the visual axis of one eye.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"strabismus","termid":"MONDO:0003432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertropia","secondary_identifiers":["DOID:9837","icd11.foundation:1382376000","NCIT:C34716","SCTID:40608009","ICD9:378.31","MEDGEN:43790","UMLS:C0020575"],"termid":"MONDO:0004893","xrefs":{"Monarch":{"xref_id":"0004893"}}}


id: FYPO:0006739
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 promoters that contain MCB sites is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:30134042","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin at gene promoter region","termid":"FYPO:0008245"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to chromatin at MCB promoters during vegetative growth","synonyms":[{"name":"normal protein localisation to chromatin at MCB promoters during vegetative growth","type":"exact"},{"name":"normal protein localization to chromatin at MCB promoters during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at MCB target genes during vegetative growth","type":"related"},{"name":"normal protein localization to chromatin at MCB-containing promoters during vegetative growth","type":"exact"}],"termid":"FYPO:0006739"}


id: PBO:0049899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERPUD2 antisense RNA 1","termid":"PBO:0049899"}


id: PR:O74398
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A prickle-like protein 4 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":"LIM domain-containing protein C4F6.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4F6.12","secondary_identifiers":["UniProtKB:O74398"],"synonyms":[{"name":"Spom972h-PRICKLE4","type":"exact"}],"termid":"PR:O74398"}


id: GO:0042144
data:
  {"annotated_genes":["SJAG_01072","SJAG_03386","SJAG_00029","SJAG_00380","SJAG_01299","SJAG_04909","SJAG_03072","SJAG_05194","SJAG_03137","SJAG_00330","SJAG_03915","SJAG_01598","SJAG_02384","SJAG_02433","SJAG_04966"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72899,93004,93131,101846,102143,102643,103015,106553,110221,111378,118814],"is_not":false,"summary":null,"term":"GO:0042144"},{"annotations":[103351],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0061192"},{"annotations":[99499,112219],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0061191"},{"annotations":[99258],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032889"}]},"cv_name":"biological_process","definition":"The fusion of two vacuole membranes to form a single vacuole.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuole fusion","termid":"GO:0097576"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00029":null,"SJAG_00330":null,"SJAG_00380":null,"SJAG_01072":null,"SJAG_01299":null,"SJAG_01598":null,"SJAG_02384":null,"SJAG_02433":null,"SJAG_03072":null,"SJAG_03137":null,"SJAG_03386":null,"SJAG_03915":null,"SJAG_04909":null,"SJAG_04966":null,"SJAG_05194":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"vacuole fusion, non-autophagic","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0042145"],"synonyms":[{"name":"homotypic vacuole fusion","type":"exact"},{"name":"homotypic vacuole fusion (non-autophagic)","type":"exact"},{"name":"homotypic vacuole fusion, non-autophagic","type":"exact"},{"name":"vacuole fusion (non-autophagic)","type":"exact"}],"termid":"GO:0042144","terms_by_termid":{"GO:0032889":null,"GO:0042144":null,"GO:0061191":null,"GO:0061192":null}}


id: GO:2000937
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellotriose catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"negative regulation of cellotriose metabolic process","termid":"GO:2000934"},{"relation_name":"is_a","term_name":"regulation of cellotriose catabolic process","termid":"GO:2000936"},{"relation_name":"negatively_regulates","term_name":"cellotriose catabolic process","termid":"GO:2000894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cellotriose catabolic process","synonyms":[{"name":"negative regulation of cellotriose catabolism","type":"exact"}],"termid":"GO:2000937"}


id: PBO:0117072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PALM2AKAP2 antisense RNA 1","termid":"PBO:0117072"}


id: GO:0035159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Ensuring that a tube in an open tracheal system is of the correct length.","definition_xrefs":["GOC:mtg_sensu","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tube size, open tracheal system","termid":"GO:0035151"}],"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 tube length, open tracheal system","synonyms":[{"name":"regulation of tracheal tube length","type":"exact"},{"name":"tracheal tube elongation","type":"narrow"}],"termid":"GO:0035159"}


id: GO:0042780
data:
  {"annotated_genes":["SJAG_03761","SJAG_04885","SJAG_01704","SJAG_02993","SJAG_00195","SJAG_02288","SJAG_00997"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94867,100352,100819],"is_not":false,"summary":null,"term":"GO:0042780"},{"annotations":[89545,71804,119917,82196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990180"},{"annotations":[72066,76587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001680"}]},"cv_name":"biological_process","definition":"The process in which the 3' end of a pre-tRNA molecule is converted to that of a mature tRNA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA processing","termid":"GO:0008033"},{"relation_name":"is_a","term_name":"RNA 3'-end processing","termid":"GO:0031123"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00195":null,"SJAG_00997":null,"SJAG_01704":null,"SJAG_02288":null,"SJAG_02993":null,"SJAG_03761":null,"SJAG_04885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006399"],"is_obsolete":false,"name":"tRNA 3'-end processing","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"tRNA 3' processing","type":"exact"}],"termid":"GO:0042780","terms_by_termid":{"GO:0001680":null,"GO:0042780":null,"GO:1990180":null}}


id: GO:0010830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of myotube differentiation. Myotube differentiation is the process in which a relatively unspecialized cell acquires specialized features of a myotube cell. Myotubes are multinucleated cells that are formed when proliferating myoblasts exit the cell cycle, differentiate and fuse.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of striated muscle cell differentiation","termid":"GO:0051153"},{"relation_name":"regulates","term_name":"myotube differentiation","termid":"GO:0014902"}],"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 myotube differentiation","termid":"GO:0010830"}


id: MONDO:0020444
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Subaortic course of innominate vein is a rare congential anomaly of the great veins characterized by an anomalous course of the left brachiocephalic vein, passing from left to right below the aortic arch and entering the superior vena cava below the orifice of the azygos vein. Patients are frequently asymptomatic and diagnosed incidentally on imaging studies. Other cardiac malformations may be associated.","definition_xrefs":["Orphanet:99113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital anomaly of superior vena cava","termid":"MONDO:0019829"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subaortic course of innominate vein","secondary_identifiers":["GARD:19656","UMLS:C4707821","MEDGEN:1637333","SCTID:766756002"],"synonyms":[{"name":"subaortic course of brachiocephalic vein","type":"exact"}],"termid":"MONDO:0020444","xrefs":{"Monarch":{"xref_id":"0020444"}}}


id: PBO:0002181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-actinin","termid":"PBO:0002181"}


id: GO:0070253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of somatostatin from secretory granules in the D cells of the pancreas.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide hormone secretion","termid":"GO:0030072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0023052","GO:0051179"],"is_obsolete":false,"name":"somatostatin secretion","termid":"GO:0070253"}


id: GO:2000454
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of CD8-positive, alpha-beta cytotoxic T cell extravasation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of CD8-positive, alpha-beta T cell extravasation","termid":"GO:2000451"},{"relation_name":"is_a","term_name":"regulation of CD8-positive, alpha-beta cytotoxic T cell extravasation","termid":"GO:2000452"},{"relation_name":"positively_regulates","term_name":"CD8-positive, alpha-beta cytotoxic T cell extravasation","termid":"GO:0035698"}],"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 CD8-positive, alpha-beta cytotoxic T cell extravasation","termid":"GO:2000454"}


id: PBO:0080789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XRCC1 N-terminal domain containing 1, N-terminal like","termid":"PBO:0080789"}


id: MONDO:0043765
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bilateral hearing loss caused by progressive degeneration of cochlear structures and central auditory pathways, typically associated with the aging process.","definition_xrefs":["NCIT:C116367"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensorineural hearing loss disorder","termid":"MONDO:0020678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"presbycusis","secondary_identifiers":["MESH:D011304","SCTID:49526009","UMLS:C0033074","MEDGEN:10911","icd11.foundation:1569854675"],"synonyms":[{"name":"ARHI","type":"exact"},{"name":"Presbycuses","type":"related"},{"name":"age-related hearing impairment","type":"exact"},{"name":"age-related hearing loss","type":"related"},{"name":"presbyacusia","type":"related"},{"name":"presbycusis","type":"exact"},{"name":"senile deafness","type":"related"}],"termid":"MONDO:0043765","xrefs":{"Monarch":{"xref_id":"0043765"}}}


id: PBO:0089959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH pyrophosphatase","termid":"PBO:0089959"}


id: PBO:0069574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 847, pseudogene","termid":"PBO:0069574"}


id: PR:O94346
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1271.14 gene.","definition_xrefs":["UniProtKB:O94346","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":"arginine biosynthesis bifunctional protein ArgJ, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1271.14","synonyms":[{"name":"Spom972h-SPBC1271.14","type":"exact"}],"termid":"PR:O94346"}


id: MONDO:0011931
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"ovarian cancer","termid":"MONDO:0008170"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian cancer, susceptibility to, 1","secondary_identifiers":["OMIM:607893","MEDGEN:390836","UMLS:C2675601"],"synonyms":[{"name":"OVCAS1","type":"exact"},{"name":"ovarian cancer, susceptibility to","type":"exact"},{"name":"ovarian cancer, susceptibility to, 1","type":"exact"}],"termid":"MONDO:0011931","xrefs":{"Monarch":{"xref_id":"0011931"}}}


id: MONDO:0013484
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cataract in which the cause of the disease is a mutation in the TDRD7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cataract","termid":"MONDO:0005129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cataract 36","secondary_identifiers":["UMLS:C3151304","MEDGEN:462654","DOID:0110247","OMIM:613887"],"synonyms":[{"name":"CATC4","type":"exact"},{"name":"CTRCT36","type":"exact"},{"name":"TDRD7 cataract (disease)","type":"exact"},{"name":"autosomal recessive congenital cataract 4","type":"exact"},{"name":"cataract (disease) caused by mutation in TDRD7","type":"exact"},{"name":"cataract 36","type":"exact"},{"name":"cataract type 36","type":"exact"},{"name":"cataract, autosomal recessive congenital 4","type":"related"}],"termid":"MONDO:0013484","xrefs":{"Monarch":{"xref_id":"0013484"}}}


id: PR:O94705
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cox9 gene.","definition_xrefs":["UniProtKB:O94705","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":"cytochrome c oxidase subunit 7A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1259.05c","synonyms":[{"name":"Spom972h-cox9","type":"exact"},{"name":"cytochrome c oxidase polypeptide VIIA (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94705"}


id: PBO:0090448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane-associated serine-rich cell wall sensor Mtl2","termid":"PBO:0090448"}


id: PBO:0038629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACKR4 pseudogene 1","termid":"PBO:0038629"}


id: SO:0002249
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A CDS region corresponding to a mature protein region of a polypeptide.","direct_ancestors":[{"relation_name":"is_a","term_name":"CDS_region","termid":"SO:0000851"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mature_protein_region_of_CDS","synonyms":[{"name":"INSDC_feature:mat_peptide","type":"exact"},{"name":"mature protein region of CDS","type":"exact"}],"termid":"SO:0002249"}


id: PBO:0069425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 689, pseudogene","termid":"PBO:0069425"}


id: GO:0021685
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the cerebellar granule layer. This process pertains to the physical shaping of a rudimentary structure. The granular layer is the innermost layer of the cerebellar cortex. This layer contains densely packed small neurons, mostly granule cells. Some Golgi cells are found at the outer border. Granule neurons send parallel fibers to the upper molecular layer, where they synapse with Purkinje cell dendrites. Mossy fibers from the pontine nuclei in the white matter synapse with granule cell axons, Golgi cell axons and unipolar brush interneuron axons at cerebellar glomeruli in the granule cell layer.","definition_xrefs":["GOC:cls","GOC:dgh","GOC:jid","GO_REF:0000021","GOC:dph","ISBN:0838580343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"cerebellar granular layer morphogenesis","termid":"GO:0021683"},{"relation_name":"part_of","term_name":"cerebellar cortex structural organization","termid":"GO:0021698"}],"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":"cerebellar granular layer structural organization","synonyms":[{"name":"cerebellar granular layer structural organisation","type":"exact"}],"termid":"GO:0021685"}


id: PBO:0075000
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 115-11","termid":"PBO:0075000"}


id: MONDO:0011530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mesomelic dysplasia, Savarirayan type is characterized by severely hypoplastic and triangular-shaped tibiae, and absence of the fibulae. So far, two sporadic cases have been described. Moderate mesomelia of the upper limbs, proximal widening of the ulnas, pelvic anomalies and marked bilateral glenoid hypoplasia were also reported.","definition_xrefs":["Orphanet:85170"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesomelic dysplasia","termid":"MONDO:0023599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"mesomelic dysplasia, Savarirayan type","secondary_identifiers":["MESH:C565349","MEDGEN:343129","icd11.foundation:1627637820","OMIM:605274","SCTID:715652002","UMLS:C1854470","GARD:10584"],"synonyms":[{"name":"mesomelic dysplasia Savarirayan type","type":"related"},{"name":"mesomelic dysplasia with absent fibulas and triangular tibias","type":"exact"},{"name":"mesomelic dysplasia, Savarirayan type","type":"exact"},{"name":"triangular tibia and fibular aplasia","type":"related"},{"name":"triangular tibia-fibular aplasia syndrome","type":"exact"}],"termid":"MONDO:0011530","xrefs":{"Monarch":{"xref_id":"0011530"}}}


id: MONDO:1011348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Post-Infectious disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post-infectious disorder, non-human animal","termid":"MONDO:1011348","xrefs":{"Monarch":{"xref_id":"1011348"}}}


id: PBO:0060403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-alpha-acetyltransferase 11, NatA catalytic subunit","termid":"PBO:0060403"}


id: PBO:0036483
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARGinine requiring","termid":"PBO:0036483"}


id: PBO:0044284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome X open reading frame 38","termid":"PBO:0044284"}


id: GO:0016312
data:
  {"annotated_genes":["SJAG_01702","SJAG_00063"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[117529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004441"},{"annotations":[110244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030487"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: myo-inositol bisphosphate + H2O = myo-inositol phosphate + phosphate.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol phosphate phosphatase activity","termid":"GO:0052745"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00063":null,"SJAG_01702":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:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016788","GO:0003824"],"is_obsolete":false,"name":"inositol bisphosphate phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-6809565","Reactome:R-HSA-6809561","RHEA:57840"],"termid":"GO:0016312","terms_by_termid":{"GO:0004441":null,"GO:0030487":null}}


id: PBO:0062541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily H member 1 pseudogene","termid":"PBO:0062541"}


id: PBO:0051011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin like growth factor 1 receptor","termid":"PBO:0051011"}


id: PBO:0048042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrous sheath interacting protein 2 like, pseudogene","termid":"PBO:0048042"}


id: PBO:0067393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 498, pseudogene","termid":"PBO:0067393"}


id: GO:1904710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of granulosa cell apoptotic process.","definition_xrefs":["GO_REF:0000058","PMID:19208546","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of epithelial cell apoptotic process","termid":"GO:1904037"},{"relation_name":"is_a","term_name":"regulation of granulosa cell apoptotic process","termid":"GO:1904708"},{"relation_name":"positively_regulates","term_name":"granulosa cell apoptotic process","termid":"GO:1904700"}],"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 granulosa cell apoptotic process","synonyms":[{"name":"activation of granulosa cell apoptosis","type":"narrow"},{"name":"activation of granulosa cell apoptotic process","type":"narrow"},{"name":"activation of granulosa cell of ovary apoptosis","type":"narrow"},{"name":"activation of granulosa cell of ovary apoptotic process","type":"narrow"},{"name":"positive regulation of granulosa cell apoptosis","type":"narrow"},{"name":"positive regulation of granulosa cell of ovary apoptosis","type":"narrow"},{"name":"positive regulation of granulosa cell of ovary apoptotic process","type":"exact"},{"name":"up regulation of granulosa cell apoptosis","type":"narrow"},{"name":"up regulation of granulosa cell apoptotic process","type":"exact"},{"name":"up regulation of granulosa cell of ovary apoptosis","type":"narrow"},{"name":"up regulation of granulosa cell of ovary apoptotic process","type":"exact"},{"name":"up-regulation of granulosa cell apoptosis","type":"narrow"},{"name":"up-regulation of granulosa cell apoptotic process","type":"exact"},{"name":"up-regulation of granulosa cell of ovary apoptosis","type":"narrow"},{"name":"up-regulation of granulosa cell of ovary apoptotic process","type":"exact"},{"name":"upregulation of granulosa cell apoptosis","type":"narrow"},{"name":"upregulation of granulosa cell apoptotic process","type":"exact"},{"name":"upregulation of granulosa cell of ovary apoptosis","type":"narrow"},{"name":"upregulation of granulosa cell of ovary apoptotic process","type":"exact"}],"termid":"GO:1904710"}


id: MONDO:1012796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any polyneuropathy that occurs in dogs due to a mutation in the NDRG1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"polyneuropathy, dog","termid":"MONDO:1012354"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyneuropathy, NDRG1-related, dog","secondary_identifiers":["OMIA:002120-9615"],"termid":"MONDO:1012796","xrefs":{"Monarch":{"xref_id":"1012796"}}}


id: MONDO:0010761
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Y-linked form of retinitis pigmentosa.","definition_xrefs":["MONDO:patterns/y_linked"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Y-linked disease","termid":"MONDO:0000428"},{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa Y-linked","secondary_identifiers":["MESH:C564035","OMIM:400004","UMLS:C1839079","ICD10CM:H35.5","GARD:15310","DOID:0110418","MEDGEN:326805"],"synonyms":[{"name":"RPY","type":"exact"},{"name":"Y-linked retinitis pigmentosa","type":"exact"},{"name":"retinitis pigmentosa, Y-linked","type":"exact"},{"name":"retinitis pigmentosa, Y-linked, Y-linked","type":"exact"}],"termid":"MONDO:0010761","xrefs":{"Monarch":{"xref_id":"0010761"}}}


id: PBO:0070260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U11 small nuclear 5, pseudogene","termid":"PBO:0070260"}


id: PBO:0049782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 17","termid":"PBO:0049782"}


id: FYPO:0000161
data:
  {"alleles_by_uniquename":{"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121219],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"}],"single_locus_phenotype":[{"annotations":[121130,121442],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002998"},{"annotations":[121208,121497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which contractile ring assembly is abnormal. Contractile ring assembly is the part of cytokinesis in which the actomyosin contractile ring is formed of actin, myosin, and associated proteins.","definition_xrefs":["GO:1903475","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cytokinesis during vegetative growth","termid":"FYPO:0000032"},{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring organization","termid":"FYPO:0004738"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01143":null,"SJAG_02392":null,"SJAG_02592":null},"genotype_count":3,"genotypes_by_uniquename":{"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0004803","FYPO:0000032","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000631"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_01143","SJAG_02392"],"name":"abnormal actomyosin contractile ring assembly","references_by_uniquename":{"PMID:25866389":null,"PMID:27059155":null,"PMID:32915139":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_01143","SJAG_02592"],"single_locus_genotype_uniquenames":["mid1delta","sty1delta"],"synonyms":[{"name":"abnormal actomyosin contractile ring assembly during mitotic cell cycle","type":"related"},{"name":"abnormal actomyosin contractile ring assembly during vegetative growth","type":"exact"},{"name":"abnormal actomyosin contractile ring formation","type":"related"},{"name":"abnormal contractile ring assembly","type":"exact"},{"name":"abnormal cytokinesis, actomyosin contractile ring assembly","type":"exact"},{"name":"abnormal cytokinetic contractile ring assembly","type":"exact"},{"name":"abnormal cytokinetic ring assembly","type":"related"},{"name":"abnormal cytokinetic ring formation","type":"related"},{"name":"abnormal mitotic contractile ring assembly","type":"exact"}],"termid":"FYPO:0000161","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYECO:0000248":null,"FYPO:0000729":null,"FYPO:0002998":null,"FYPO_EXT:0000001":null}}


id: MONDO:0004999
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete chondrosarcoma (obsolete MONDO:0004999)","termid":"MONDO:0004999","xrefs":{"Monarch":{"xref_id":"0004999"}}}


id: PBO:0066992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 295","termid":"PBO:0066992"}


id: FYPO:0004761
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 histone exchange occurs to a greater extent than normal in regions of pericentric heterochromatin. Histone exchange is replacement, within chromatin, of resident histones or histone subunits with alternative, sometimes variant, histones or subunits.","definition_xrefs":["GO:0043486","PomBase:mah","PMID:24095277","GO:0005721"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin remodeling","termid":"FYPO:0006356"},{"relation_name":"is_a","term_name":"increased protein exchange at pericentric heterochromatin","termid":"FYPO:0006360"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0000641","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"increased histone exchange at pericentric heterochromatin","synonyms":[{"name":"increased histone exchange at dh repeat","type":"narrow"},{"name":"increased histone exchange at pericentric heterochromatin during mitotic cell cycle","type":"related"},{"name":"increased histone exchange at pericentric heterochromatin during vegetative growth","type":"exact"}],"termid":"FYPO:0004761"}


id: GO:0032985
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of a protein-carbohydrate complex into its constituent components.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex disassembly","termid":"GO:0032984"},{"relation_name":"is_a","term_name":"protein-carbohydrate complex subunit organization","termid":"GO:0071823"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein-carbohydrate complex disassembly","termid":"GO:0032985"}


id: MONDO:0002622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary bone osteosarcoma affecting multiple bone sites.","definition_xrefs":["NCIT:C6470"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteosarcoma","termid":"MONDO:0009807"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"multifocal osteogenic sarcoma","secondary_identifiers":["MEDGEN:233199","UMLS:C1334820","DOID:3360"],"synonyms":[{"name":"multicentric osteosarcoma","type":"exact"},{"name":"multifocal osteosarcoma","type":"exact"}],"termid":"MONDO:0002622","xrefs":{"Monarch":{"xref_id":"0002622"}}}


id: MONDO:0004474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma that arises from the gallbladder, with the bulk of the tumor located at this site.","definition_xrefs":["NCIT:C5734"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastrointestinal lymphoma","termid":"MONDO:0004699"},{"relation_name":"is_a","term_name":"gallbladder cancer","termid":"MONDO:0005411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005570","MONDO:0002515","MONDO:0004992"],"is_obsolete":false,"name":"gallbladder lymphoma","secondary_identifiers":["DOID:8135","MEDGEN:232224","UMLS:C1333748"],"synonyms":[{"name":"gall bladder lymphoma","type":"exact"},{"name":"gallbladder lymphoma","type":"exact"},{"name":"lymphoma of gall bladder","type":"exact"},{"name":"lymphoma of gallbladder","type":"exact"},{"name":"lymphoma of the gallbladder","type":"exact"},{"name":"primary gallbladder lymphoma","type":"exact"}],"termid":"MONDO:0004474","xrefs":{"Monarch":{"xref_id":"0004474"}}}


id: FYPO:0000787
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 trimethylation of lysine at position 9 of histone H3 is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002274","FYPO:0005447","FYPO:0002494","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal histone H3-K9 trimethylation during vegetative growth","synonyms":[{"name":"abnormal histone H3 K9 trimethylation during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K9 trimethylation during mitotic cell cycle","type":"related"},{"name":"abnormal histone H3K9 trimethylation during vegetative growth","type":"exact"},{"name":"abnormal histone H3K9me3 during vegetative growth","type":"exact"},{"name":"abnormal histone lysine H3 K9 trimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000787"}


id: PBO:0069205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 460, pseudogene","termid":"PBO:0069205"}


id: MONDO:1012329
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"laminitis, non-human animal","termid":"MONDO:1011767"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laminitis, ass","secondary_identifiers":["OMIA:001225-9793"],"termid":"MONDO:1012329","xrefs":{"Monarch":{"xref_id":"1012329"}}}


id: MONDO:0019696
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of extremely rare, inherited, progressive skeletal conditions that result in a particular form of short stature, called short-limb dwarfism. The short stature is the result of unusually short forearms and forelegs (mesomelia) and abnormal shortening of the bones in the hands and feet (acromelia). At birth, the hands and feet may appear abnormally short and broad. Over time, the apparent disproportion becomes even more obvious, especially during the first years of life. Additional features may include: limited extension of the elbows and arms; progressive abnormal curvature of the spine; an enlarged head; and a slightly flattened midface. Acromesomelic dysplasia is inherited as an autosomal recessive trait. There are different types of acromesomelic dysplasia, which are distinguished by their genetic cause. To read more about the different types, click on the links below. Acromesomelic dysplasia, Maroteaux type Acromesomelic dysplasia, Hunter-Thompson type Acromesomelic dysplasia, Grebe type","definition_xrefs":["GARD:0000006"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"acromesomelic dysplasia","secondary_identifiers":["DOID:0080049","Orphanet:93437","UMLS:C5235036","GARD:6","OMIMPS:602875","icd11.foundation:2002361676","MESH:C535658","MEDGEN:1710812","NORD:724"],"synonyms":[{"name":"acromesomelic dwarfism","type":"related"}],"termid":"MONDO:0019696","xrefs":{"Monarch":{"xref_id":"0019696"}}}


id: PR:O13802
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ebp2 gene.","definition_xrefs":["UniProtKB:O13802","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":"rRNA-processing protein ebp2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17H9.05","synonyms":[{"name":"Spom972h-ebp2","type":"exact"}],"termid":"PR:O13802"}


id: FYPO:0000263
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A gene expression phenotype in which regulation of translation in response to stress is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to stress","termid":"FYPO:0000162"},{"relation_name":"is_a","term_name":"translation regulation phenotype","termid":"FYPO:0000289"},{"relation_name":"is_a","term_name":"abnormal gene expression","termid":"FYPO:0006551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0005447","FYPO:0000298","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal regulation of translation in response to stress","synonyms":[{"name":"protein synthesis after stress, defective","type":"related"}],"termid":"FYPO:0000263"}


id: GO:0097400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-17 binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:21602493","GOC:ic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"},{"relation_name":"part_of","term_name":"cellular response to interleukin-17","termid":"GO:0097398"}],"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":"interleukin-17-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-448424"],"synonyms":[{"name":"IL-17-mediated signaling pathway","type":"exact"},{"name":"IL-17-mediated signalling pathway","type":"exact"},{"name":"interleukin-17-mediated signalling pathway","type":"exact"}],"termid":"GO:0097400"}


id: PBO:0084698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial flavin adenine dinucleotide transporter; FAD is a synthesis product of riboflavin; human homolog SLC25A32 is implicated in multiple acyl-CoA dehydrogenase deficiency (MADD) or glutaric aciduria type II (GAII), and can complement yeast null mutant","termid":"PBO:0084698"}


id: PBO:0074716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 77","termid":"PBO:0074716"}


id: SO:1001260
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A Shine-Dalgarno sequence that stimulates recoding through interactions with the anti-Shine-Dalgarno in the RNA of small ribosomal subunits of translating ribosomes. The signal is only operative in Bacteria.","definition_xrefs":["SO:ke","PMID:12519954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"internal_ribosome_entry_site","termid":"SO:0000243"},{"relation_name":"is_a","term_name":"recoding_stimulatory_region","termid":"SO:1001268"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"internal_Shine_Dalgarno_sequence","synonyms":[{"name":"internal Shine Dalgarno sequence","type":"exact"},{"name":"internal Shine-Dalgarno sequence","type":"exact"}],"termid":"SO:1001260"}


id: GO:0075037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of symbiont appressorium maturation.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of appressorium maturation (obsolete GO:0075037)","synonyms":[{"name":"positive regulation maturation of appressorium on or near host","type":"exact"},{"name":"positive regulation of appressorium maturation on or near host","type":"related"}],"termid":"GO:0075037"}


id: PBO:0053891
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 1173","termid":"PBO:0053891"}


id: PBO:0081129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFP1 zinc finger protein","termid":"PBO:0081129"}


id: PBO:0055251
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 2678","termid":"PBO:0055251"}


id: GO:0072751
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 L-thialysine stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amino acid stimulus","termid":"GO:0071230"},{"relation_name":"is_a","term_name":"response to L-thialysine","termid":"GO:1901345"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to L-thialysine","synonyms":[{"name":"cellular response to thialysine","type":"broad"}],"termid":"GO:0072751"}


id: GO:0005803
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A small subcellular vesicle, or granule, surrounded by a single-layered membrane; formed from the Golgi apparatus and contains a highly concentrated protein destined for secretion.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete secretory vesicle (obsolete GO:0005803)","synonyms":[{"name":"secretory vesicle","type":"exact"},{"name":"transition vesicle","type":"narrow"}],"termid":"GO:0005803"}


id: GO:1904443
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of thyroid gland epithelial cell proliferation.","definition_xrefs":["PMID:17646383","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of epithelial cell proliferation","termid":"GO:0050679"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of thyroid gland epithelial cell proliferation","termid":"GO:1904441"},{"relation_name":"positively_regulates","term_name":"thyroid gland epithelial cell proliferation","termid":"GO:1990789"}],"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 thyroid gland epithelial cell proliferation","synonyms":[{"name":"activation of Hurthle cell proliferation","type":"narrow"},{"name":"activation of thyroid follicular cell proliferation","type":"narrow"},{"name":"activation of thyroid gland epithelial cell proliferation","type":"narrow"},{"name":"positive regulation of Hurthle cell proliferation","type":"narrow"},{"name":"positive regulation of thyroid follicular cell proliferation","type":"narrow"},{"name":"up regulation of Hurthle cell proliferation","type":"narrow"},{"name":"up regulation of thyroid follicular cell proliferation","type":"narrow"},{"name":"up regulation of thyroid gland epithelial cell proliferation","type":"exact"},{"name":"up-regulation of Hurthle cell proliferation","type":"narrow"},{"name":"up-regulation of thyroid follicular cell proliferation","type":"narrow"},{"name":"up-regulation of thyroid gland epithelial cell proliferation","type":"exact"},{"name":"upregulation of Hurthle cell proliferation","type":"narrow"},{"name":"upregulation of thyroid follicular cell proliferation","type":"narrow"},{"name":"upregulation of thyroid gland epithelial cell proliferation","type":"exact"}],"termid":"GO:1904443"}


id: PBO:0044434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily A member 43, pseudogene","termid":"PBO:0044434"}


id: RO:0003309
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between an entity (e.g. a chemical, environmental exposure, or some form of genetic variation) and a condition (a phenotype or disease), where the presence of the entity worsens some or all aspects of the condition.","direct_ancestors":[{"relation_name":"is_a","term_name":"contributes_to_severity_of_condition","termid":"RO:0003305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exacerbates_condition","termid":"RO:0003309"}


id: PBO:0081359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 185 with LIM domain","termid":"PBO:0081359"}


id: GO:0000095
data:
  {"annotated_genes":["SJAG_01589","SJAG_01890"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77916,81978],"is_not":false,"summary":null,"term":"GO:0000095"}]},"cv_name":"molecular_function","definition":"Enables the transfer of S-adenosylmethionine from one side of a membrane to the other. S-adenosylmethionine is S-(5'-adenosyl)-L-methionine, an important intermediate in one-carbon metabolism.","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":"sulfur compound transmembrane transporter activity","termid":"GO:1901682"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01589":null,"SJAG_01890":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"S-adenosyl-L-methionine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0015177","Reactome:R-HSA-8855062"],"synonyms":[{"name":"S-adenosyl methionine permease activity","type":"exact"},{"name":"S-adenosyl methionine transporter activity","type":"exact"},{"name":"S-adenosylmethionine permease activity","type":"exact"},{"name":"S-adenosylmethionine transmembrane transporter activity","type":"exact"},{"name":"S-adenosylmethionine transporter activity","type":"broad"},{"name":"SAM transmembrane transporter activity","type":"exact"}],"termid":"GO:0000095","terms_by_termid":{"GO:0000095":null}}


id: PBO:0083199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the verified gene MMS4","termid":"PBO:0083199"}


id: GO:0061451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the retrotrapezoid nucleus (RTN) over time from it's initial formation to its mature state. The retrotrapezoid nucleus is a group of neurons in the rostral medulla, which are responsible regulating respiration.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"medulla oblongata development","termid":"GO:0021550"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"retrotrapezoid nucleus development","termid":"GO:0061451"}


id: MONDO:0060551
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":"cerebellar atrophy, developmental delay, and seizures","secondary_identifiers":["MEDGEN:1626119","OMIM:617643","UMLS:C4539985"],"synonyms":[{"name":"CADEDS","type":"related"},{"name":"cerebellar atrophy, developmental delay, and seizures","type":"exact"}],"termid":"MONDO:0060551","xrefs":{"Monarch":{"xref_id":"0060551"}}}


id: FYPO:0006278
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the structure of an O-linked glycan moiety of a nascent or mature glycoprotein differs from wild type.","definition_xrefs":["PMID:22988247","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glycoprotein glycan structure","termid":"FYPO:0003290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0002274"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0002494"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0003290"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0002274","FYPO:0002494","FYPO:0003290"],"is_obsolete":false,"name":"abnormal O-linked glycoprotein glycan structure","synonyms":[{"name":"abnormal O-linked glycoprotein oligosaccharide structure","type":"related"}],"termid":"FYPO:0006278"}


id: PBO:0005507
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae GPI8","termid":"PBO:0005507"}


id: PBO:0089888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transposon fragment","termid":"PBO:0089888"}


id: PBO:0050470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOXA cluster antisense RNA 2","termid":"PBO:0050470"}


id: GO:0010306
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of rhamnogalacturonan II, a low molecular mass (5 - 10KDa) pectic polysaccharide, conserved in the primary walls of dicotyledenous and monocotyledenous plants and gymnosperms.","definition_xrefs":["PMID:12754267"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhamnogalacturonan II metabolic process","termid":"GO:0010396"},{"relation_name":"is_a","term_name":"cell wall pectin biosynthetic process","termid":"GO:0052325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"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","GO:0005975"],"is_obsolete":false,"name":"rhamnogalacturonan II biosynthetic process","termid":"GO:0010306"}


id: PBO:0000759
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene structure uopdated","termid":"PBO:0000759"}


id: PBO:0016537
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae YPR081C","termid":"PBO:0016537"}


id: FYPO:0003667
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which crossover junction endodeoxyribonuclease activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal crossover junction endodeoxyribonuclease activity","termid":"FYPO:0003666"},{"relation_name":"is_a","term_name":"abolished endodeoxyribonuclease activity","termid":"FYPO:0007141"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0000661","FYPO:0000002","FYPO:0000654","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished crossover junction endodeoxyribonuclease activity","synonyms":[{"name":"crossover junction endodeoxyribonuclease activity abolished","type":"exact"}],"termid":"FYPO:0003667"}


id: GO:0031473
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a class III myosin; myosin III is monomeric and has an N terminal kinase domain.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myosin binding","termid":"GO:0017022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008092"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0008092","GO:0003674"],"is_obsolete":false,"name":"myosin III binding","termid":"GO:0031473"}


id: PBO:0076416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 9","termid":"PBO:0076416"}


id: FYPO:0002830
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, begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein phosphorylation during vegetative growth","termid":"FYPO:0000775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"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:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0002274","FYPO:0000002","FYPO:0001320","FYPO:0002494"],"is_obsolete":false,"name":"delayed onset of protein phosphorylation during vegetative growth","synonyms":[{"name":"delayed onset of protein phosphorylation during mitotic cell cycle","type":"related"},{"name":"delayed onset of protein/peptide phosphorylation during vegetative growth","type":"exact"},{"name":"delayed protein phosphorylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002830"}


id: MOD:02062
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an N-formyl-L-methionine residue crosslinked to one or more amino acid residues.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified N-formyl-L-methionine residue","termid":"MOD:01450"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crosslinked N-formyl-L-methionine residue","termid":"MOD:02062"}


id: GO:1900158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of bone mineralization involved in bone maturation.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of bone mineralization","termid":"GO:0030502"},{"relation_name":"is_a","term_name":"regulation of bone mineralization involved in bone maturation","termid":"GO:1900157"},{"relation_name":"negatively_regulates","term_name":"bone mineralization involved in bone maturation","termid":"GO:0035630"}],"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 bone mineralization involved in bone maturation","synonyms":[{"name":"down regulation of bone mineralization involved in bone maturation","type":"exact"},{"name":"down-regulation of bone mineralization involved in bone maturation","type":"exact"},{"name":"downregulation of bone mineralization involved in bone maturation","type":"exact"},{"name":"inhibition of bone mineralization involved in bone maturation","type":"narrow"}],"termid":"GO:1900158"}


id: GO:0060973
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a cell from one site to another that will contribute to the progression of the heart over time, from its initial formation, to the mature organ.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"heart development","termid":"GO:0007507"}],"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":"cell migration involved in heart development","termid":"GO:0060973"}


id: PBO:0041279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1q and TNF related 5","termid":"PBO:0041279"}


id: PBO:0054248
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 1630","termid":"PBO:0054248"}


id: PBO:0040603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B melanoma antigen","termid":"PBO:0040603"}


id: GO:1905430
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 glycine stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:18984164"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amino acid stimulus","termid":"GO:0071230"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to glycine","termid":"GO:1905429"}],"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 glycine","synonyms":[{"name":"cellular response to Gly","type":"exact"},{"name":"cellular response to aminoacetic acid","type":"exact"},{"name":"cellular response to aminoethanoic acid","type":"exact"},{"name":"cellular response to glycin","type":"exact"}],"termid":"GO:1905430"}


id: PR:000050456
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An RNA-binding protein rnc1 (Schizosaccharomyces pombe) that has not been phosphorylated at positions equivalent to Thr-45, Thr-50, Thr-171, Thr-177, Ser-278, and Ser-286 of the amino acid sequence represented by UniProtKB:O74919. Example: UniProtKB:O74919, Thr-45/Thr-50/Thr-171/Thr-177/Ser-278/Ser-286, PR:000026291.","definition_xrefs":["PRO:DAN","PomBase:VW","PMID:31911490"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA-binding protein rnc1 (Schizosaccharomyces pombe)","termid":"PR:000050452"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rnc1/UnPhos:(T45,T50,T171,T177,S278,S286)","pombase_gene_id":"SPCC757.09c","synonyms":[{"name":"PomBase_original_PRO_term_name: RNA-binding protein rnc1 unphosphorylated 2 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-rnc1/UnPhos:2","type":"exact"},{"name":"UniProtKB:O74919, Thr-45/Thr-50/Thr-171/Thr-177/Ser-278/Ser-286, PR:000026291","type":"narrow"},{"name":"rnc1/UnPhos:(T45,T50,T171,T177,S278,S286)","type":"exact"}],"termid":"PR:000050456"}


id: PBO:0050970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon omega 1 pseudogene 5","termid":"PBO:0050970"}


id: PBO:0027696
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_curved_cytoplasmic_microtubules","termid":"PBO:0027696"}


id: MONDO:0001406
data:
  {"annotated_genes":["SJAG_02398","SJAG_00260","SJAG_01671","SJAG_03920","SJAG_01895","SJAG_03163","SJAG_01111","SJAG_04213"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008192"},{"annotations":[88834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[88744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011544"},{"annotations":[87448],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[87656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"},{"annotations":[88980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032771"},{"annotations":[89124,89123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024517"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm arising from a peripheral nerve or the perineural sheaths.","definition_xrefs":["NCIT:C3321"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral nervous system disorder","termid":"MONDO:0003620"},{"relation_name":"is_a","term_name":"nervous system neoplasm","termid":"MONDO:0021248"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_01111":null,"SJAG_01671":null,"SJAG_01895":null,"SJAG_02398":null,"SJAG_03163":null,"SJAG_03920":null,"SJAG_04213":null},"genotype_count":0,"is_obsolete":false,"name":"peripheral nervous system neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:45817","ICD9:239.2","DOID:1192","UMLS:C0031118","SCTID:126980002","MESH:D010524","ONCOTREE:PNS","EFO:0002431"],"synonyms":[{"name":"CNS-excluded nervous sys. cancer","type":"narrow"},{"name":"PNS neoplasm","type":"exact"},{"name":"PNS neoplasms","type":"exact"},{"name":"PNS tumor","type":"exact"},{"name":"PNS tumour","type":"exact"},{"name":"neoplasm of PNS","type":"exact"},{"name":"neoplasm of peripheral nerve","type":"exact"},{"name":"neoplasm of peripheral nervous system","type":"exact"},{"name":"neoplasm of the PNS","type":"exact"},{"name":"neoplasm of the peripheral nerve","type":"exact"},{"name":"neoplasm of the peripheral nervous system","type":"exact"},{"name":"neoplasms, PNS","type":"exact"},{"name":"neoplasms, peripheral nervous system","type":"exact"},{"name":"nerve sheath neoplasm","type":"narrow"},{"name":"nerve sheath tumors","type":"narrow"},{"name":"nerve sheath tumours","type":"narrow"},{"name":"peripheral nerve neoplasm","type":"exact"},{"name":"peripheral nerve tumor","type":"exact"},{"name":"peripheral nerve tumour","type":"exact"},{"name":"peripheral nervous system neoplasm","type":"exact"},{"name":"peripheral nervous system neoplasm (disease)","type":"exact"},{"name":"peripheral nervous system tumor","type":"exact"},{"name":"peripheral nervous system tumour","type":"exact"},{"name":"tumor of PNS","type":"exact"},{"name":"tumor of peripheral nerve","type":"exact"},{"name":"tumor of peripheral nervous system","type":"exact"},{"name":"tumor of the PNS","type":"exact"},{"name":"tumor of the peripheral nerve","type":"exact"},{"name":"tumor of the peripheral nervous system","type":"exact"},{"name":"tumour of PNS","type":"exact"},{"name":"tumour of peripheral nerve","type":"exact"},{"name":"tumour of peripheral nervous system","type":"exact"},{"name":"tumour of the PNS","type":"exact"},{"name":"tumour of the peripheral nerve","type":"exact"},{"name":"tumour of the peripheral nervous system","type":"exact"}],"termid":"MONDO:0001406","terms_by_termid":{"MONDO:0007273":null,"MONDO:0008192":null,"MONDO:0011121":null,"MONDO:0011544":null,"MONDO:0013602":null,"MONDO:0024517":null,"MONDO:0032771":null},"xrefs":{"Monarch":{"xref_id":"0001406"}}}


id: PBO:0110416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSBP3 pseudogene 6","termid":"PBO:0110416"}


id: PBO:0081447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 311","termid":"PBO:0081447"}


id: PBO:0065912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RABGAP1L divergent transcript","termid":"PBO:0065912"}


id: GO:0034396
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the rate of transcription from an RNA polymerase II promoter in response to an iron stimulus.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transcription from RNA polymerase II promoter in response to iron (obsolete GO:0034396)","synonyms":[{"name":"down regulation of transcription from RNA polymerase II promoter in response to iron","type":"exact"},{"name":"down-regulation of transcription from RNA polymerase II promoter in response to iron","type":"exact"},{"name":"downregulation of transcription from RNA polymerase II promoter in response to iron","type":"exact"},{"name":"inhibition of transcription from RNA polymerase II promoter in response to iron","type":"narrow"},{"name":"negative regulation of transcription from Pol II promoter in response to iron","type":"exact"}],"termid":"GO:0034396"}


id: PBO:0039113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activator of HSP90 ATPase homolog 2, pseudogene","termid":"PBO:0039113"}


id: PBO:0069329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 588, pseudogene","termid":"PBO:0069329"}


id: PBO:0029055
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_degradation_during_nitrogen_starvation","termid":"PBO:0029055"}


id: MONDO:1012600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cystinuria that occurs in cats due to a mutation in the SLC3A1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cystinuria, non-human animal","termid":"MONDO:1012968"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystinuria, SLC3A1-related, domestic cat","secondary_identifiers":["OMIA:000256-9685"],"synonyms":[{"name":"cystinuria, type I - A, domestic cat","type":"related"}],"termid":"MONDO:1012600","xrefs":{"Monarch":{"xref_id":"1012600"}}}


id: PR:Q9URU2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA replication ATP-dependent helicase/nuclease DNA2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03776","PANTHER:PTHR10887:SF14","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA replication ATP-dependent helicase/nuclease dna2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16D10.04c","secondary_identifiers":["UniProtKB:Q9URU2"],"synonyms":[{"name":"Spom972h-DNA2","type":"exact"}],"termid":"PR:Q9URU2"}


id: PBO:0086710
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; MINDY family deubiquitinase that does not appear to contain catalytic activity; predicted prenylation/proteolysis target of Afc1p and Rce1p; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus; not an essential gene; YGL082W has a paralog, YPL191C, that arose from the whole genome duplication; ortholog of human MINDY1/FAM63A","termid":"PBO:0086710"}


id: FYPO:0005219
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a transcript, i.e. an RNA molecule synthesized on a DNA template by RNA polymerase, is shorter than normal.","definition_xrefs":["PomBase:mah","PMID:26582768","SO:0000673"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transcript length","termid":"FYPO:0003048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0003048"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0001985","FYPO:0003048"],"is_obsolete":false,"name":"decreased transcript length","synonyms":[{"name":"short transcript","type":"exact"},{"name":"shortened transcript","type":"exact"}],"termid":"FYPO:0005219"}


id: MONDO:0100501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare anomaly (1 in 14,000 to 42,000 pregnancies; 1 in 7500 fetuses from 10 to 14 weeks of gestation) characterized by a complex anomaly of the anterior abdominal wall, severe kyphoscoliosis, rudimentary umbilical cord, and anatomical defects of the pelvis and lower limbs.","definition_xrefs":["PMID:33115503"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abdominal wall malformation","termid":"MONDO:0100298"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"body-stalk anomaly","synonyms":[{"name":"BSA","type":"exact"},{"name":"LBWC","type":"narrow"},{"name":"body stalk anomaly","type":"exact"},{"name":"body stalk complex","type":"exact"},{"name":"limb body wall complex","type":"narrow"}],"termid":"MONDO:0100501","xrefs":{"Monarch":{"xref_id":"0100501"}}}


id: PBO:0084847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the large subunit; homologous to bacterial L16 ribosomal protein; synthetic lethality with hac1 mutation suggests a possible role in synthesis of precursors for protein glycosylation","termid":"PBO:0084847"}


id: GO:0099104
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases the activity of a potassium channel, resulting in its opening.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium channel regulator activity","termid":"GO:0015459"},{"relation_name":"is_a","term_name":"channel activator activity","termid":"GO:0099103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140677","GO:0003674","GO:0098772"],"is_obsolete":false,"name":"potassium channel activator activity","termid":"GO:0099104"}


id: GO:0052439
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism modulates the frequency, rate or extent of the deposition of callose by the symbiont in its cell walls, occurring as part of the defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of defense-related symbiont cell wall callose deposition (obsolete GO:0052439)","synonyms":[{"name":"modulation by organism of defense-related symbiont cell wall callose deposition","type":"exact"}],"termid":"GO:0052439"}


id: MONDO:0015892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Growth hormone insensitivity syndrome (GHIS) is a group of diseases characterized by marked short stature associated with normal or elevated growth hormone (GH) concentrations, which fail to respond to exogenous GH administration. GHIS comprises growth delay due to IGF-1 deficiency, growth delay due to IGF-1 resistance, Laron syndrome, short stature due to STAT5b deficiency and primary acid-labile subunit (ALS) deficiency.","definition_xrefs":["Orphanet:181393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary endocrine growth disease","termid":"MONDO:0015514"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth hormone insensitivity syndrome","secondary_identifiers":["GARD:3924","NANDO:2200321","NCIT:C129867","NANDO:2100114","UMLS:C4318479","MEDGEN:1384226"],"synonyms":[{"name":"GHIS","type":"exact"},{"name":"Growth hormone insensitivity syndromes","type":"exact"},{"name":"short stature due to a defect in growth hormone receptor or post-receptor pathway","type":"exact"}],"termid":"MONDO:0015892","xrefs":{"Monarch":{"xref_id":"0015892"}}}


id: MONDO:0021950
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune oophoritis is a rare cause of primary ovarian insufficiency (POI). It happens when the body's immune system mistakenly attacks the ovaries causing inflammation, atrophy and fibrosis. These changes stop the ovaries from working normally. The main symptoms of autoimmune oophorotis are irregular or absent menstrual period (amenorrhea) and symptoms related to ovarian cysts such as abdominal cramping, bloating, nausea and vomiting. Autoimmune oophoritis may occur as part of autoimmune polyglandular syndrome type I and type II but has also been associated with lupus, pernicious anemia, myasthenia gravis and other autoimmune conditions. The underlying cause of autoimmune oophoritis is unknown. Diagnosis involves a special blood test which looks for anti-steroid or anti-ovarian antibodies, a pelvic ultrasound to look for enlarged cystic ovaries and tests to rule out other possible causes of POI. Management of autoimmune oophoritis involves emotional support, possible estrogen replacement therapy and management of other autoimmune conditions.","definition_xrefs":["GARD:0009461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of endocrine system","termid":"MONDO:0000569"},{"relation_name":"is_a","term_name":"oophoritis","termid":"MONDO:0006877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune oophoritis","secondary_identifiers":["UMLS:C0878654","MEDGEN:163900","MESH:C538274"],"termid":"MONDO:0021950","xrefs":{"Monarch":{"xref_id":"0021950"}}}


id: PBO:0056514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscleblind like splicing regulator 3","termid":"PBO:0056514"}


id: GO:0061457
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a cell from the mesonephros to the male gonad, contributing to its development.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"}],"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":"mesonephric cell migration involved in male gonad development","termid":"GO:0061457"}


id: FYECO:0000463
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"The assay, or growth of cells, was conducted in the presence of light.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping experimental environment","termid":"FYECO:0000132"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"presence of light","termid":"FYECO:0000463"}


id: GO:0052709
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of N-alpha,N-alpha,N-alpha-trimethyl-L-histidine, also known as histidine betaine or hercynine, a trimethylated derivative of histidine.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid betaine biosynthetic process","termid":"GO:0006578"},{"relation_name":"is_a","term_name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine metabolic process","termid":"GO:0052708"},{"relation_name":"is_a","term_name":"L-amino acid biosynthetic process","termid":"GO:0170034"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid biosynthetic process","termid":"GO:0170043"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine biosynthetic process","synonyms":[{"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine anabolism","type":"exact"},{"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine biosynthesis","type":"exact"},{"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine formation","type":"exact"},{"name":"N-alpha,N-alpha,N-alpha-trimethyl-L-histidine synthesis","type":"exact"},{"name":"hercynine anabolism","type":"exact"},{"name":"hercynine biosynthesis","type":"exact"},{"name":"hercynine biosynthetic process","type":"exact"},{"name":"hercynine formation","type":"exact"},{"name":"hercynine synthesis","type":"exact"},{"name":"histidine betaine anabolism","type":"exact"},{"name":"histidine betaine biosynthesis","type":"exact"},{"name":"histidine betaine biosynthetic process","type":"exact"},{"name":"histidine betaine formation","type":"exact"},{"name":"histidine betaine synthesis","type":"exact"}],"termid":"GO:0052709"}


id: PBO:0043352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLPTM1L pseudogene 1","termid":"PBO:0043352"}


id: PBO:0064713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 49","termid":"PBO:0064713"}


id: PBO:0057829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR3147 host gene","termid":"PBO:0057829"}


id: PBO:0058420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4789","termid":"PBO:0058420"}


id: GO:0140989
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7-deoxyloganate + O2 + reduced [NADPH-hemoprotein reductase] = H+ + H2O + loganate + oxidized [NADPH-hemoprotein reductase].","definition_xrefs":["RHEA:57576","PMID:24710322"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"7-deoxyloganate 7-hydroxylase activity","termid":"GO:0140989"}


id: GO:0071403
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 high density lipoprotein particle stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to lipoprotein particle stimulus","termid":"GO:0071402"}],"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 high density lipoprotein particle stimulus","secondary_identifiers":["GO:0055099"],"synonyms":[{"name":"cellular response to high-density lipoprotein particle stimulus","type":"exact"},{"name":"response to high density lipoprotein particle","type":"broad"},{"name":"response to high density lipoprotein particle stimulus","type":"broad"}],"termid":"GO:0071403"}


id: PBO:0083581
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; transcription is AZF1 dependent in glycerol-lactate medium and SLT2 dependent in response to the lipid hydroperoxides","termid":"PBO:0083581"}


id: GO:0017039
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the release of an N-terminal dipeptide from a peptide comprising four or more residues, with broad specificity; also acts on dipeptidyl 2-naphthylamides.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete dipeptidyl-peptidase III activity (obsolete GO:0017039)","synonyms":[{"name":"DPP III activity","type":"related"},{"name":"dipeptidyl aminopeptidase III activity","type":"related"},{"name":"dipeptidyl arylamidase III activity","type":"related"},{"name":"dipeptidyl-peptidase III activity","type":"exact"},{"name":"enkephalinase B activity","type":"narrow"},{"name":"red cell angiotensinase activity","type":"narrow"}],"termid":"GO:0017039"}


id: MONDO:1012057
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"degenerative myopathy of deep pectoral muscle, non-human animal","termid":"MONDO:1011787"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"degenerative myopathy of deep pectoral muscle, turkey","secondary_identifiers":["OMIA:000264-9103"],"termid":"MONDO:1012057","xrefs":{"Monarch":{"xref_id":"1012057"}}}


id: PBO:0081560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 484","termid":"PBO:0081560"}


id: PBO:0061082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NKX2-1 antisense RNA 1","termid":"PBO:0061082"}


id: PBO:0054368
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 1762","termid":"PBO:0054368"}


id: GO:0032724
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of fractalkine production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of fractalkine production","termid":"GO:0032644"},{"relation_name":"is_a","term_name":"positive regulation of chemokine production","termid":"GO:0032722"},{"relation_name":"positively_regulates","term_name":"fractalkine production","termid":"GO:0032603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of fractalkine production","synonyms":[{"name":"activation of fractalkine production","type":"narrow"},{"name":"stimulation of fractalkine production","type":"narrow"},{"name":"up regulation of fractalkine production","type":"exact"},{"name":"up-regulation of fractalkine production","type":"exact"},{"name":"upregulation of fractalkine production","type":"exact"}],"termid":"GO:0032724"}


id: GO:0033869
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a nucleoside bisphosphate, a compound consisting of a nucleobase linked to a deoxyribose or ribose sugar esterified with one phosphate group attached to each of two different hydroxyl groups on the sugar.","definition_xrefs":["GOC:pde","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside bisphosphate metabolic process","termid":"GO:0033865"},{"relation_name":"is_a","term_name":"nucleoside phosphate catabolic process","termid":"GO:1901292"}],"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:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"nucleoside bisphosphate catabolic process","synonyms":[{"name":"nucleoside bisphosphate breakdown","type":"exact"},{"name":"nucleoside bisphosphate catabolism","type":"exact"},{"name":"nucleoside bisphosphate degradation","type":"exact"}],"termid":"GO:0033869"}


id: PBO:0090046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S29","termid":"PBO:0090046"}


id: GO:0003024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events by which a decrease in diameter of an artery is detected and converted to a molecular signal.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"baroreceptor detection of arterial stretch","termid":"GO:0001981"},{"relation_name":"part_of","term_name":"baroreceptor response to decreased systemic arterial blood pressure","termid":"GO:0001982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"baroreceptor detection of decreased arterial stretch","termid":"GO:0003024"}


id: GO:0035119
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring in the embryo, by which the anatomical structures of the pelvic fin are generated and organized. The pelvic fins are bilaterally paired fins mounted in a ventral-lateral position on most fish. These fins are used primarily for lateral mobility and propulsion.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic appendage morphogenesis","termid":"GO:0035113"},{"relation_name":"is_a","term_name":"pelvic fin morphogenesis","termid":"GO:0035139"}],"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":"embryonic pelvic fin morphogenesis","termid":"GO:0035119"}


id: PR:Q9URZ4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cat1 gene.","definition_xrefs":["UniProtKB:Q9URZ4","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":"cationic amino acid transporter 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC869.11","synonyms":[{"name":"Spom972h-cat1","type":"exact"}],"termid":"PR:Q9URZ4"}


id: PBO:0008883
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 Mm/Mi","termid":"PBO:0008883"}


id: FYPO:0000288
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype that affects the regulation of gene expression.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene expression phenotype","termid":"FYPO:0000142"},{"relation_name":"is_a","term_name":"regulation phenotype","termid":"FYPO:0000145"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"gene expression regulation phenotype","synonyms":[{"name":"fission yeast gene expression regulation phenotype","type":"exact"}],"termid":"FYPO:0000288"}


id: PBO:0040757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B double prime 1 pseudogene","termid":"PBO:0040757"}


id: PBO:0063997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 31","termid":"PBO:0063997"}


id: PR:O74848
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug146 gene.","definition_xrefs":["UniProtKB:O74848","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":"meiotically up-regulated gene 146 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.12c","synonyms":[{"name":"Spom972h-mug146","type":"exact"}],"termid":"PR:O74848"}


id: GO:2001146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity.","definition_xrefs":["GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity (obsolete GO:2001146)","termid":"GO:2001146"}


id: GO:0030429
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-kynurenine + H2O = anthranilate + L-alanine + H+. Also acts on 3'-hydroxykynurenine and some other (3-arylcarbonyl)- alanines.","definition_xrefs":["EC:3.7.1.3","PMID:17300176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances","termid":"GO:0016823"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"kynureninase activity","secondary_identifiers":["MetaCyc:KYNURENINASE-RXN","Reactome:R-HSA-71217"],"synonyms":[{"name":"L-kynurenine hydrolase activity","type":"related"},{"name":"kynurenine hydrolase activity","type":"related"}],"termid":"GO:0030429"}


id: GO:0070820
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A secretory granule that contains cathepsin and gelatinase and is readily exocytosed upon cell activation; found primarily in mature neutrophil cells.","definition_xrefs":["PMID:12070036","GOC:mah","GOC:rl","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule","termid":"GO:0030141"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0031410","GO:0005575"],"is_obsolete":false,"name":"tertiary granule","synonyms":[{"name":"gelatinase granule","type":"exact"}],"termid":"GO:0070820"}


id: GO:0005942
data:
  {"annotated_genes":["SJAG_04552","SJAG_04860","SJAG_01876","SJAG_03403","SJAG_02699","SJAG_00114"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[113480,79058,96479,78543,73310],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034271"},{"annotations":[107633,78544,79059,73311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034272"}]},"cv_name":"cellular_component","definition":"A protein complex capable of phosphatidylinositol 3-kinase activity and containing subunits of any phosphatidylinositol 3-kinase (PI3K) enzyme. These complexes are divided in three classes (called I, II and III) that differ for their presence across taxonomic groups and for the type of their constituents. Catalytic subunits of phosphatidylinositol 3-kinase enzymes are present in all 3 classes; regulatory subunits of phosphatidylinositol 3-kinase enzymes are present in classes I and III; adaptor proteins have been observed in class II complexes and may be present in other classes too.","definition_xrefs":["GOC:bf","PMID:24587488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex, transferring phosphorus-containing groups","termid":"GO:0061695"},{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"extrinsic component of membrane","termid":"GO:0019898"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_01876":null,"SJAG_02699":null,"SJAG_03403":null,"SJAG_04552":null,"SJAG_04860":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"phosphatidylinositol 3-kinase complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"1-phosphatidylinositol 3-kinase complex","type":"exact"},{"name":"PI3-kinase p85-subunit alpha- PI3-kinase p110 complex","type":"narrow"},{"name":"PI3K complex","type":"exact"},{"name":"PIK3C3-PIK3R4 complex","type":"narrow"},{"name":"PIK3CA-PIK3R1 complex","type":"narrow"},{"name":"phosphoinositide 3-kinase complex","type":"exact"}],"termid":"GO:0005942","terms_by_termid":{"GO:0034271":null,"GO:0034272":null}}


id: MONDO:0014950
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial thoracic aortic aneurysm and aortic dissection in which the cause of the disease is a mutation in the LOX gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial thoracic aortic aneurysm and aortic dissection","termid":"MONDO:0019625"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aortic aneurysm, familial thoracic 10","secondary_identifiers":["UMLS:C4284414","MEDGEN:924785","GARD:16207","OMIM:617168"],"synonyms":[{"name":"AAT10","type":"exact"},{"name":"LOX familial thoracic aortic aneurysm and aortic dissection","type":"exact"},{"name":"aortic aneurysm, familial thoracic 10","type":"exact"},{"name":"aortic aneurysm, familial thoracic type 10","type":"exact"},{"name":"familial thoracic aortic aneurysm and aortic dissection caused by mutation in LOX","type":"exact"}],"termid":"MONDO:0014950","xrefs":{"Monarch":{"xref_id":"0014950"}}}


id: PBO:0091632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pdc2-Repressed lncRNA, pdc102-antisense","termid":"PBO:0091632"}


id: PBO:0048760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"germ cell-less 1, spermatogenesis associated","termid":"PBO:0048760"}


id: GO:0052909
data:
  {"annotated_genes":["SJAG_02821"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70107],"is_not":false,"summary":null,"term":"GO:0052909"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 4 S-adenosyl-L-methionine + adenine(1779)/adenine(1780) in 18S rRNA = 4 S-adenosyl-L-homocysteine + N(6)-dimethyladenine(1779)/N(6)-dimethyladenine(1780) in 18S rRNA.","definition_xrefs":["RHEA:42780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA (adenine-N6,N6-)-dimethyltransferase activity","termid":"GO:0000179"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02821":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0140098","GO:0003824","GO:0016741","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"18S rRNA (adenine(1779)-N(6)/adenine(1780)-N(6))-dimethyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["MetaCyc:RXN-11634","EC:2.1.1.183"],"synonyms":[{"name":"M(6)(2)A dimethylase activity","type":"broad"}],"termid":"GO:0052909","terms_by_termid":{"GO:0052909":null}}


id: PBO:0004017
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer, hereditary nonpolyposis colon","termid":"PBO:0004017"}


id: GO:0060535
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of cartilage in the trachea are generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cartilage morphogenesis","termid":"GO:0060536"},{"relation_name":"part_of","term_name":"trachea morphogenesis","termid":"GO:0060439"},{"relation_name":"part_of","term_name":"trachea cartilage development","termid":"GO:0060534"}],"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":"trachea cartilage morphogenesis","termid":"GO:0060535"}


id: GO:0008222
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete tumor antigen (obsolete GO:0008222)","synonyms":[{"name":"tumor antigen","type":"exact"}],"termid":"GO:0008222"}


id: PBO:0031155
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transport","termid":"PBO:0031155"}


id: PBO:0082154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adaptor protein for various signaling pathways; involved in mating response, invasive/filamentous growth, osmotolerance; acts as an adaptor that links G protein-associated Cdc42p-Ste20p complex to the effector Ste11p to modulate signal transduction","termid":"PBO:0082154"}


id: PBO:0003401
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae YGL056C and YBR214W","termid":"PBO:0003401"}


id: MONDO:0004960
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition characterized by the abnormal presence of monoclonal immunoglobulins in the blood or urine.","definition_xrefs":["NCIT:C35548"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"plasma cell neoplasm","termid":"MONDO:0004959"},{"relation_name":"is_a","term_name":"hematologic disorder","termid":"MONDO:0005570"}],"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":"monoclonal gammopathy","secondary_identifiers":["UMLS:C1136085","ICD10CM:D47.2","MESH:D010265","EFO:0000203","SCTID:109983007","MEDGEN:210153"],"termid":"MONDO:0004960","xrefs":{"Monarch":{"xref_id":"0004960"}}}


id: SO:0000191
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An intron that is not the most 3-prime or the most 5-prime in a given transcript.","direct_ancestors":[{"relation_name":"is_a","term_name":"intron","termid":"SO:0000188"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interior_intron","synonyms":[{"name":"interior intron","type":"exact"}],"termid":"SO:0000191"}


id: MONDO:0009907
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":"Prepapillary vascular loops","secondary_identifiers":["MESH:C563287","OMIM:264060","UMLS:C1828066","SCTID:424728002","MEDGEN:316814"],"synonyms":[{"name":"Prepapillary vascular loops","type":"exact"},{"name":"preretinal vascular loops","type":"related"}],"termid":"MONDO:0009907","xrefs":{"Monarch":{"xref_id":"0009907"}}}


id: GO:1903036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of response to wounding.","definition_xrefs":["GO_REF:0000058","GOC:kmv","GOC:TermGenie","PMID:19164535"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"is_a","term_name":"regulation of response to wounding","termid":"GO:1903034"},{"relation_name":"positively_regulates","term_name":"response to wounding","termid":"GO:0009611"}],"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 response to wounding","synonyms":[{"name":"activation of physiological response to wounding","type":"narrow"},{"name":"activation of response to wounding","type":"narrow"},{"name":"positive regulation of physiological response to wounding","type":"exact"},{"name":"up regulation of physiological response to wounding","type":"exact"},{"name":"up regulation of response to wounding","type":"exact"},{"name":"up-regulation of physiological response to wounding","type":"exact"},{"name":"up-regulation of response to wounding","type":"exact"},{"name":"upregulation of physiological response to wounding","type":"exact"},{"name":"upregulation of response to wounding","type":"exact"}],"termid":"GO:1903036"}


id: PBO:0072675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RTRAF pseudogene 2","termid":"PBO:0072675"}


id: PBO:0084214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Homodimeric subunit of autophagy-specific PtdIns-3-kinase complex I; required for the integrity of the active PtdIns-3-kinase complex I by maintaining an association between Vps15p-Vps34p and Atg14p-Vps30p subcomplexes; localizes to the pre-autophagosomal structure (PAS) in an Atg14p-dependent manner; ATG38 is non-essential but is required for macroautophagy","termid":"PBO:0084214"}


id: FYPO:0002522
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transport phenotype observed in the vegetative growth phase of the life cycle in which the export of polyadenylated mRNA from the nucleus is decreased. Export of all polyadenylated mRNAs or a specific mRNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"increased nuclear polyadenylated mRNA level during vegetative growth","termid":"FYPO:0003119"},{"relation_name":"is_a","term_name":"abnormal poly(A)+ mRNA export from nucleus","termid":"FYPO:0000183"},{"relation_name":"is_a","term_name":"decreased nuclear export","termid":"FYPO:0000508"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0006551","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"decreased poly(A)+ mRNA export from nucleus","synonyms":[{"name":"decreased poly(A)+ mRNA export from nucleus during mitotic cell cycle","type":"related"},{"name":"decreased poly(A)+ mRNA export from nucleus during vegetative growth","type":"exact"},{"name":"decreased polyadenylated mRNA export from nucleus","type":"exact"},{"name":"reduced poly(A)+ mRNA export from nucleus","type":"exact"}],"termid":"FYPO:0002522"}


id: GO:0031058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the covalent alteration of a histone.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone modification (obsolete GO:0031058)","synonyms":[{"name":"activation of histone modification","type":"narrow"},{"name":"stimulation of histone modification","type":"narrow"},{"name":"up regulation of histone modification","type":"exact"},{"name":"up-regulation of histone modification","type":"exact"},{"name":"upregulation of histone modification","type":"exact"}],"termid":"GO:0031058"}


id: MONDO:0020095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal dominant form of disease with focal palmoplantar keratoderma as a major feature.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature (obsolete MONDO:0020095)","secondary_identifiers":["Orphanet:98353"],"synonyms":[{"name":"autosomal dominant disease associated with focal palmoplantar hyperkeratosis as a major feature","type":"exact"},{"name":"autosomal dominant disease with focal palmoplantar keratoderma as a major feature","type":"exact"},{"name":"disease with focal palmoplantar keratoderma as a major feature, autosomal dominant","type":"exact"}],"termid":"MONDO:0020095","xrefs":{"Monarch":{"xref_id":"0020095"}}}


id: MONDO:0015493
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary lipodystrophy","termid":"MONDO:0020087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy","secondary_identifiers":["Orphanet:156156"],"termid":"MONDO:0015493","xrefs":{"Monarch":{"xref_id":"0015493"}}}


id: _global:capable_of_negatively_regulating
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"Holds between c and p if and only if c is capable of some activity a, and a negatively regulates p.","direct_ancestors":[{"relation_name":"is_a","term_name":"capable_of_regulating","termid":"_global:capable_of_regulating"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capable_of_negatively_regulating","secondary_identifiers":["RO:0002597"],"termid":"_global:capable_of_negatively_regulating"}


id: PBO:0038821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 24, pseudogene","termid":"PBO:0038821"}


id: GO:0009634
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete heavy metal sensitivity/resistance (obsolete GO:0009634)","synonyms":[{"name":"heavy metal sensitivity/resistance","type":"exact"}],"termid":"GO:0009634"}


id: GO:1905033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of membrane repolarization during cardiac muscle cell action potential.","definition_xrefs":["GOC:rph","GOC:BHF","GOC:BHF_miRNA","GOC:TermGenie","PMID:23157812","GO_REF:0000058","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of biological process","termid":"GO:0048518"},{"relation_name":"is_a","term_name":"regulation of membrane repolarization during cardiac muscle cell action potential","termid":"GO:1905031"},{"relation_name":"positively_regulates","term_name":"membrane repolarization during cardiac muscle cell action potential","termid":"GO:0086013"}],"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 membrane repolarization during cardiac muscle cell action potential","synonyms":[{"name":"activation of membrane repolarization during cardiac muscle cell action potential","type":"narrow"},{"name":"up regulation of membrane repolarization during cardiac muscle cell action potential","type":"exact"},{"name":"up-regulation of membrane repolarization during cardiac muscle cell action potential","type":"exact"},{"name":"upregulation of membrane repolarization during cardiac muscle cell action potential","type":"exact"}],"termid":"GO:1905033"}


id: PBO:0062748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily J member 3","termid":"PBO:0062748"}


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":["RESID:AA0445","PubMed:6893271","PubMed:6010785","ChEBI:141823"],"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: SO:0001284
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"2-thiocytidine is a modified cytidine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytidine","termid":"SO:0001275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"two_thiocytidine","secondary_identifiers":["RNAMOD:023"],"synonyms":[{"name":"2-thiocytidine","type":"exact"},{"name":"s2C","type":"exact"},{"name":"two thiocytidine","type":"exact"}],"termid":"SO:0001284"}


id: PBO:0060025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 13","termid":"PBO:0060025"}


id: GO:0036508
data:
  {"annotated_genes":["SJAG_01858"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904380"}]},"cv_name":"biological_process","definition":"The removal of one or more alpha 1,2-linked mannose residues from a mannosylated protein.","definition_xrefs":["GOC:PARL","GOC:bf","PMID:21062743","PMID:25092655"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein demannosylation","termid":"GO:0036507"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01858":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein alpha-1,2-demannosylation","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"glycoprotein mannose trimming","type":"related"},{"name":"mannose trimming","type":"broad"}],"termid":"GO:0036508","terms_by_termid":{"GO:1904380":null}}


id: PBO:0030724
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_membrane_organization","termid":"PBO:0030724"}


id: MONDO:0005207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant tumor arising from trophoblastic cells. The vast majority of cases arise in the uterus and represent gestational choriocarcinomas that derive from placental trophoblastic cells. Approximately half of the cases develop from a complete hydatidiform mole. A minority of cases arise in the testis or the ovaries. There is often marked elevation of human chorionic gonadotropin (hCG) in the blood. Choriocarcinomas disseminate rapidly through the hematogenous route; the lungs are most frequently affected.","definition_xrefs":["NCIT:C2948"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"placenta cancer","termid":"MONDO:0002178"},{"relation_name":"excluded_subClassOf","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"trophoblastic neoplasm","termid":"MONDO:0002872"},{"relation_name":"is_a","term_name":"germ cell tumor","termid":"MONDO:0005040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choriocarcinoma","secondary_identifiers":["ICDO:9100/3","NANDO:2200070","EFO:0002893","UMLS:C0008497","ONCOTREE:BCCA","HP:0100768","MEDGEN:40278","GARD:6059","MESH:D002822","SCTID:188188009","DOID:3594"],"synonyms":[{"name":"chorioblastoma","type":"exact"},{"name":"choriocarcinoma","type":"exact"},{"name":"choriocarcinoma (disease)","type":"exact"},{"name":"choriocarcinoma, malignant","type":"exact"},{"name":"chorioepithelioma","type":"exact"},{"name":"chorion carcinoma","type":"exact"},{"name":"chorionic carcinoma","type":"exact"}],"termid":"MONDO:0005207","xrefs":{"Monarch":{"xref_id":"0005207"}}}


id: PBO:0049362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 21","termid":"PBO:0049362"}


id: GO:0180015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of nucleoside from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:21998139","PMID:30658162"],"direct_ancestors":[{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"nucleoside transmembrane transport","termid":"GO:1901642"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"nucleoside import across plasma membrane","termid":"GO:0180015"}


id: PBO:0087258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine/threonine protein kinase; regulates the orientation checkpoint, the morphogenesis checkpoint and the metabolic switch from fermentative to oxidative metabolism by phosphorylating the activation loop of Kin4p, Hsl1p and Snf1p respectively; cooperates with Hsl7p in recruiting Hsl1p to the septin ring, a prerequisite for subsequent recruitment, phosphorylation, and degradation of Swe1p; forms part of the bud neck ring; regulates cytokinesis","termid":"PBO:0087258"}


id: PR:Q6MX60
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBCPT2R1.02 gene.","definition_xrefs":["UniProtKB:Q6MX60","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein CPT2R1.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBCPT2R1.02","synonyms":[{"name":"Spom972h-SPBCPT2R1.02","type":"exact"}],"termid":"PR:Q6MX60"}


id: PBO:0049479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H1.3 linker histone, cluster member","termid":"PBO:0049479"}


id: PBO:0069673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 950, pseudogene","termid":"PBO:0069673"}


id: MONDO:0019138
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bleeding diathesis due to a collagen receptor defect (obsolete MONDO:0019138)","secondary_identifiers":["Orphanet:73271"],"termid":"MONDO:0019138","xrefs":{"Monarch":{"xref_id":"0019138"}}}


id: PBO:0042184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin B2","termid":"PBO:0042184"}


id: PBO:0079804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP glucuronosyltransferase family 2 member B25, pseudogene","termid":"PBO:0079804"}


id: MONDO:0008898
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Camptodactyly syndrome, Guadalajara type 1 is a rare syndrome consisting of growth retardation, facial dysmorphism, camptodactyly and skeletal anomalies.","definition_xrefs":["Orphanet:1327"],"direct_ancestors":[{"relation_name":"is_a","term_name":"camptodactyly syndrome, Guadalajara","termid":"MONDO:0000111"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"camptodactyly syndrome, Guadalajara type 1","secondary_identifiers":["GARD:1067","UMLS:C1859359","MESH:C537970","SCTID:720602007","OMIM:211910","MEDGEN:395241"],"synonyms":[{"name":"FTSS","type":"related"},{"name":"GCS 1","type":"related"},{"name":"GCS1","type":"related"},{"name":"camptodactyly syndrome Guadalajara type 1","type":"related"},{"name":"camptodactyly syndrome, Guadalajara, type 1","type":"related"},{"name":"camptodactyly syndrome, Guadalajara, type I","type":"related"},{"name":"faciothoracoskeletal syndrome","type":"related"}],"termid":"MONDO:0008898","xrefs":{"Monarch":{"xref_id":"0008898"}}}


id: GO:0106060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of exit from mitosis.","definition_xrefs":["PMID:11493649","GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of meiotic cell cycle phase transition","termid":"GO:1901993"},{"relation_name":"regulates","term_name":"exit from meiosis","termid":"GO:1990947"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of exit from meiosis","termid":"GO:0106060"}


id: MONDO:0034212
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chemotherapy-induced toxicity","termid":"MONDO:0800390"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methotrexate toxicity","secondary_identifiers":["Orphanet:565782","UMLS:C0568062","MEDGEN:108272"],"termid":"MONDO:0034212","xrefs":{"Monarch":{"xref_id":"0034212"}}}


id: FYPO:0005558
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the amount, distribution, or morphology of microtubule bundles is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton","termid":"FYPO:0002399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0002399","FYPO:0000054"],"is_obsolete":false,"name":"abnormal microtubule bundle","secondary_identifiers":["FYPO:0005795"],"synonyms":[{"name":"abnormal MT bundle","type":"exact"},{"name":"abnormal microtubule array","type":"related"},{"name":"abnormal microtubule bundle physical object quality","type":"exact"},{"name":"abnormal microtubule bundle structure","type":"narrow"}],"termid":"FYPO:0005558"}


id: PBO:0062529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily U member 9","termid":"PBO:0062529"}


id: GO:0097134
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of cyclin E1 and cyclin-dependent kinase 2 (CDK2). Cyclins are characterized by periodicity in protein abundance throughout the cell cycle. Cyclin-dependent kinases represent a family of serine/threonine protein kinases that become active upon binding to a cyclin regulatory partner.","definition_xrefs":["GOC:so","PMID:15935619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclin-dependent protein kinase holoenzyme complex","termid":"GO:0000307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"cyclin E1-CDK2 complex","termid":"GO:0097134"}


id: PBO:0074617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 17B","termid":"PBO:0074617"}


id: PBO:0110334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP5PF pseudogene 4","termid":"PBO:0110334"}


id: GO:0030191
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Stops, prevents or reduces the activity of chaperones of the Hsp70/Hsc70 class.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete Hsp70/Hsc70 protein inhibitor activity (obsolete GO:0030191)","synonyms":[{"name":"Hsp70/Hsc70 protein inhibitor activity","type":"exact"}],"termid":"GO:0030191"}


id: PBO:0077922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPT1 pseudogene 13","termid":"PBO:0077922"}


id: PBO:0059149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGUK p55 scaffold protein 1","termid":"PBO:0059149"}


id: GO:0022037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the metencephalon over time, from its formation to the mature structure.","definition_xrefs":["GOC:cls","GOC:jid","GO_REF:0000021","GOC:curators","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"hindbrain development","termid":"GO:0030902"}],"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":"metencephalon development","termid":"GO:0022037"}


id: MONDO:0015477
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pinnae fistula or cyst is a rare otorhinolaryngological malformation characterized by the presence of a, usually unilateral, sinus tract or cyst located in the vicinity of the auricle (most frequently identified by a small pit near the anterior margin of the first ascending portion of the helix). Typically, patients are asymptomatic and usually only present symptoms (pain, erythema, discharge from pit) in relation to infection. Renal and inner ear anomalies may be associated.","definition_xrefs":["Orphanet:155838"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysts and fistulae of the face and oral cavity","termid":"MONDO:0015476"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pinnae fistula or cyst","secondary_identifiers":["GARD:19974","MEDGEN:1842452","UMLS:C5680633"],"termid":"MONDO:0015477","xrefs":{"Monarch":{"xref_id":"0015477"}}}


id: PBO:0005548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk33 (predicted)","termid":"PBO:0005548"}


id: GO:0033916
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1->4)-beta-D-galactosidic linkages in agarose, giving the tetramer as the predominant product.","definition_xrefs":["EC:3.2.1.81"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016798"],"is_obsolete":false,"name":"beta-agarase activity","synonyms":[{"name":"AgaA","type":"related"},{"name":"AgaB","type":"related"},{"name":"agarase activity","type":"broad"},{"name":"agarose 3-glycanohydrolase activity","type":"broad"},{"name":"agarose 4-glycanohydrolase activity","type":"related"}],"termid":"GO:0033916"}


id: PBO:0062417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 53 pseudogene","termid":"PBO:0062417"}


id: MONDO:0006167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lung carcinoma characterized by the presence of large or small neuroendocrine carcinoma cells in combination with malignant glandular or squamous epithelial cells.","definition_xrefs":["NCIT:C7591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroendocrine carcinoma","termid":"MONDO:0002120"},{"relation_name":"is_a","term_name":"lung carcinoma","termid":"MONDO:0005138"},{"relation_name":"is_a","term_name":"lung neuroendocrine neoplasm","termid":"MONDO:0005454"},{"relation_name":"is_a","term_name":"malignant mixed neoplasm","termid":"MONDO:0005853"}],"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":"combined lung carcinoma","secondary_identifiers":["UMLS:C1333123","MEDGEN:234166","EFO:1000200"],"synonyms":[{"name":"combined carcinoma of lung","type":"exact"},{"name":"combined carcinoma of the lung","type":"exact"},{"name":"combined lung cancer","type":"exact"},{"name":"combined lung carcinoma","type":"exact"}],"termid":"MONDO:0006167","xrefs":{"Monarch":{"xref_id":"0006167"}}}


id: GO:0070756
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interleukin-35 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytokine production","termid":"GO:0001819"},{"relation_name":"is_a","term_name":"regulation of interleukin-35 production","termid":"GO:0070754"},{"relation_name":"positively_regulates","term_name":"interleukin-35 production","termid":"GO:0070753"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of interleukin-35 production","secondary_identifiers":["GO:0070752"],"synonyms":[{"name":"activation of interleukin-35 production","type":"narrow"},{"name":"positive regulation of IL-35 production","type":"exact"},{"name":"positive regulation of interleukin-35 biosynthetic process","type":"narrow"},{"name":"stimulation of interleukin-35 production","type":"narrow"},{"name":"up regulation of interleukin-35 production","type":"exact"},{"name":"up-regulation of interleukin-35 production","type":"exact"},{"name":"upregulation of interleukin-35 production","type":"exact"}],"termid":"GO:0070756"}


id: SO:0000440
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A replicon that has been modified to act as a vector for foreign sequence.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"replicon","termid":"SO:0001235"},{"relation_name":"part_of","term_name":"clone","termid":"SO:0000151"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vector_replicon","secondary_identifiers":["http://en.wikipedia.org/wiki/Vector_(molecular_biology)"],"synonyms":[{"name":"vector","type":"exact"},{"name":"vector replicon","type":"exact"}],"termid":"SO:0000440"}


id: PBO:0011127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell surface glycoprotein, adhesion molecule (predicted), DUF1773 family protein 1","termid":"PBO:0011127"}


id: MONDO:0975826
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arthrogryposis multiplex congenita 7, X-linked","secondary_identifiers":["OMIM:301127"],"termid":"MONDO:0975826","xrefs":{"Monarch":{"xref_id":"0975826"}}}


id: PBO:0070328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, Ro60-associated Y4","termid":"PBO:0070328"}


id: PBO:0058878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 10394","termid":"PBO:0058878"}


id: MONDO:0000150
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spondylometaphyseal dysplasia (obsolete MONDO:0000150)","termid":"MONDO:0000150","xrefs":{"Monarch":{"xref_id":"0000150"}}}


id: GO:0039682
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process of unidirectional viral DNA replication that takes place on a circular DNA to rapidly produce numerous copies of the viral genome. Involves creating a nick in one strand of the circular DNA molecule at the origin of replication. DNA is then synthesized by DNA polymerase. Using the non-nicked strand as a template, replication proceeds around the circular DNA molecule, displacing the nicked strand as single-stranded DNA.","definition_xrefs":["VZ:915","GOC:bf","Wikipedia:Rolling_circle_replication","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral DNA strand displacement replication","termid":"GO:0039687"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"rolling circle viral DNA replication","termid":"GO:0039682"}


id: PBO:0087396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Strand exchange protein; forms helical filament with DNA that searches for homology; involved in recombinational repair of DNA DSBs during vegetative growth and meiosis; phosphorylation by Cdc28p in G2/M phase promotes DNA binding, strand invasion, and primer extension; L1 and L2 motifs of DNA binding site I have critical roles in ensuring DNA fidelity during meiotic recombination; RAD51 and RAD4 pathways confer resistance to benzo[a]pyrene dihydrodiol; homolog of Dmc1p and bacterial RecA","termid":"PBO:0087396"}


id: PBO:0049450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GXYLT1 pseudogene 4","termid":"PBO:0049450"}


id: MONDO:0025096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A herpesvirus infection of cattle characterized by catarrhal inflammation of the upper respiratory and alimentary epithelia, keratoconjunctivitis, encephalitis and lymph node enlargement. Syn: bovine epitheliosis, snotsiekte.","definition_xrefs":["MESH:D008304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cattle disease","termid":"MONDO:0024913"},{"relation_name":"is_a","term_name":"Herpesviridae infectious disease, non-human animal","termid":"MONDO:0700214"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malignant catarrh","secondary_identifiers":["SCTID:24043009"],"synonyms":[{"name":"Catarrhs, malignant","type":"related"},{"name":"catarrh, malignant","type":"related"},{"name":"catarrhal fever, malignant","type":"related"},{"name":"catarrhal fevers, malignant","type":"related"},{"name":"fever, malignant catarrhal","type":"related"},{"name":"fevers, malignant catarrhal","type":"related"},{"name":"malignant Catarrhs","type":"related"},{"name":"malignant catarrhal fever","type":"related"},{"name":"malignant catarrhal fevers","type":"related"}],"termid":"MONDO:0025096","xrefs":{"Monarch":{"xref_id":"0025096"}}}


id: PBO:0060418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acylethanolamine acid amidase","termid":"PBO:0060418"}


id: PBO:0091359
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dpb4-interacting, RRM and IDR-containing factor","termid":"PBO:0091359"}


id: MONDO:1010675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anotia that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anotia, non-human animal","termid":"MONDO:1010090"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anotia, cattle","secondary_identifiers":["OMIA:001411-9913"],"termid":"MONDO:1010675","xrefs":{"Monarch":{"xref_id":"1010675"}}}


id: GO:0045828
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving isoprenoid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of isoprenoid metabolic process","termid":"GO:0019747"},{"relation_name":"is_a","term_name":"positive regulation of lipid metabolic process","termid":"GO:0045834"},{"relation_name":"positively_regulates","term_name":"isoprenoid metabolic process","termid":"GO:0006720"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"positive regulation of isoprenoid metabolic process","synonyms":[{"name":"activation of isoprenoid metabolic process","type":"narrow"},{"name":"positive regulation of isoprenoid metabolism","type":"exact"},{"name":"stimulation of isoprenoid metabolic process","type":"narrow"},{"name":"up regulation of isoprenoid metabolic process","type":"exact"},{"name":"up-regulation of isoprenoid metabolic process","type":"exact"},{"name":"upregulation of isoprenoid metabolic process","type":"exact"}],"termid":"GO:0045828"}


id: MONDO:0020743
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute leukemia of ambiguous lineage. It is characterized by the presence of either separate populations of blasts of more than one lineage, or one population of blasts co-expressing markers of more than one lineage.","definition_xrefs":["NCIT:C82179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute leukemia of ambiguous lineage","termid":"MONDO:0019460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"mixed phenotype acute leukemia","secondary_identifiers":["UMLS:C2826025","GARD:17972","MedDRA:10067399","MEDGEN:417342","NANDO:2200018","Orphanet:530995"],"synonyms":[{"name":"MPAL","type":"exact"},{"name":"mixed phenotype acute leukemia","type":"exact"}],"termid":"MONDO:0020743","xrefs":{"Monarch":{"xref_id":"0020743"}}}


id: GO:0030734
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + 1,4-N1-D-glucooligosaccharide = S-adenosyl-L-homocysteine + oligosaccharide containing 6-methyl-D-glucose units.","definition_xrefs":["EC:2.1.1.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016741","GO:0003674"],"is_obsolete":false,"name":"polysaccharide O-methyltransferase activity","secondary_identifiers":["MetaCyc:POLYSACCHARIDE-O-METHYLTRANSFERASE-RXN"],"synonyms":[{"name":"S-adenosyl-L-methionine:1,4-alpha-D-glucan 6-O-methyltransferase activity","type":"related"},{"name":"acylpolysacharide 6-methyltransferase activity","type":"related"},{"name":"polysaccharide methyltransferase activity","type":"related"}],"termid":"GO:0030734"}


id: GO:0045702
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of spermatid nuclear differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle organization","termid":"GO:0010638"},{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"regulation of spermatid nuclear differentiation","termid":"GO:0045700"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"spermatid nucleus differentiation","termid":"GO:0007289"}],"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 spermatid nuclear differentiation","synonyms":[{"name":"activation of spermatid nuclear differentiation","type":"narrow"},{"name":"stimulation of spermatid nuclear differentiation","type":"narrow"},{"name":"up regulation of spermatid nuclear differentiation","type":"exact"},{"name":"up-regulation of spermatid nuclear differentiation","type":"exact"},{"name":"upregulation of spermatid nuclear differentiation","type":"exact"}],"termid":"GO:0045702"}


id: MONDO:0008081
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibromatosis","termid":"MONDO:0021061"}],"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":"neurofibromatosis, type IV, of Riccardi","secondary_identifiers":["MEDGEN:67393","UMLS:C0220695","MESH:C537392","OMIM:162270"],"synonyms":[{"name":"NF4","type":"related"},{"name":"Nf 4","type":"related"},{"name":"neurofibromatosis type 4","type":"exact"},{"name":"neurofibromatosis type IV","type":"exact"},{"name":"neurofibromatosis, atypical","type":"related"},{"name":"neurofibromatosis, type IV, of RICCARDI","type":"related"},{"name":"neurofibromatosis, type IV, of Riccardi","type":"exact"},{"name":"neurofibromatosis, variant form(S) of","type":"related"},{"name":"type IV neurofibromatosis of Riccardi","type":"exact"}],"termid":"MONDO:0008081","xrefs":{"Monarch":{"xref_id":"0008081"}}}


id: GO:0070738
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the posttranslational transfer of one or more glycine residues to a specific glutamate residue on a target tubulin molecule; acts on alpha or beta tubulin.","definition_xrefs":["GOC:mah","PMID:19524510"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-glycine ligase activity","termid":"GO:0070735"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0003674","GO:0016874"],"is_obsolete":false,"name":"tubulin-glycine ligase activity","synonyms":[{"name":"tubulin glycylase activity","type":"exact"}],"termid":"GO:0070738"}


id: PBO:0048964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycoprotein A33","termid":"PBO:0048964"}


id: MONDO:1010304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Synovial chondromatosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm, non-human animal","termid":"MONDO:0700098"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synovial chondromatosis, non-human animal","secondary_identifiers":["OMIA:001174"],"termid":"MONDO:1010304","xrefs":{"Monarch":{"xref_id":"1010304"}}}


id: GO:0034663
data:
  {"annotated_genes":["SJAG_02875","SJAG_00790"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72561,80458],"is_not":false,"summary":null,"term":"GO:0034663"}]},"cv_name":"cellular_component","definition":"A protein complex that is located in the endoplasmic reticulum and is composed of chaperone proteins, including BiP, GRP94; CaBP1, protein disulfide isomerase (PDI), ERdj3, cyclophilin B, ERp72, GRP170, UDP-glucosyltransferase, and SDF2-L1.","definition_xrefs":["PMID:12475965"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum protein-containing complex","termid":"GO:0140534"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00790":null,"SJAG_02875":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005783","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"endoplasmic reticulum chaperone complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"ER chaperone complex","type":"exact"},{"name":"ER network complex","type":"related"},{"name":"endoplasmic reticulum network complex","type":"related"}],"termid":"GO:0034663","terms_by_termid":{"GO:0034663":null}}


id: MONDO:0100327
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of bile acid synthesis","termid":"MONDO:0019218"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"hypercholanemia, familial","secondary_identifiers":["MEDGEN:334689","OMIMPS:607748","UMLS:C1843139"],"synonyms":[{"name":"familial hypercholanemia","type":"exact"},{"name":"hypercholanemia, familial","type":"exact"}],"termid":"MONDO:0100327","xrefs":{"Monarch":{"xref_id":"0100327"}}}


id: MONDO:0014830
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the SLFN14 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"}],"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":"platelet-type bleeding disorder 20","secondary_identifiers":["GARD:18491","UMLS:C4310797","DOID:0111055","OMIM:616913","MEDGEN:934764","Orphanet:466806"],"synonyms":[{"name":"BDPLT20","type":"exact"},{"name":"SLFN14 inherited bleeding disorder, platelet-type","type":"exact"},{"name":"autosomal dominant thrombocytopenia with platelet secretion defect","type":"exact"},{"name":"bleeding disorder, platelet-type, 20","type":"exact"},{"name":"inherited bleeding disorder, platelet-type caused by mutation in SLFN14","type":"exact"}],"termid":"MONDO:0014830","xrefs":{"Monarch":{"xref_id":"0014830"}}}


id: MONDO:0021005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare developmental disorder characterized by facial, limbs and genital features, and a disproportionate acromelic short stature. This includes X-linked, AR and AD forms of Aarskog syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"faciodigitogenital syndrome","secondary_identifiers":["MedDRA:10067148","DOID:0111824","GARD:4775","Orphanet:915"],"synonyms":[{"name":"Aarskog syndrome","type":"narrow"},{"name":"Aarskog-Scott syndrome","type":"narrow"},{"name":"faciogenital dysplasia","type":"related"}],"termid":"MONDO:0021005","xrefs":{"Monarch":{"xref_id":"0021005"}}}


id: GO:0010979
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, frequency or extent of vitamin D 24-hydroxylase activity. Vitamin D 24-hydroxylase activity catalyzes the hydroxylation of C-24 of any form of vitamin D.","definition_xrefs":["GOC:dph","GOC:BHF","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of vitamin D 24-hydroxylase activity (obsolete GO:0010979)","termid":"GO:0010979"}


id: GO:0003922
data:
  {"annotated_genes":["SJAG_00964","SJAG_04634"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95266],"is_not":false,"summary":null,"term":"GO:0003922"},{"annotations":[76469],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0003921"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + XMP + L-glutamine + H2O = AMP + diphosphate + GMP + L-glutamate + 2H+.","definition_xrefs":["RHEA:11680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-nitrogen ligase activity, with glutamine as amido-N-donor","termid":"GO:0016884"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00964":null,"SJAG_04634":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:0016874"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"GMP synthase (glutamine-hydrolyzing) activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-73792","Reactome:R-HSA-9748957","EC:6.3.5.2","Wikipedia:GMP_synthase_(glutamine-hydrolysing)","MetaCyc:GMP-SYN-GLUT-RXN"],"synonyms":[{"name":"GMP synthase (glutamine-hydrolysing)","type":"related"},{"name":"GMP synthetase (glutamine-hydrolysing)","type":"related"},{"name":"GMP synthetase (glutamine-hydrolyzing) activity","type":"related"},{"name":"glutamine amidotransferase activity","type":"related"},{"name":"guanosine 5'-monophosphate synthetase activity","type":"related"},{"name":"guanosine monophosphate synthetase (glutamine-hydrolyzing)","type":"related"},{"name":"guanylate synthetase (glutamine-hydrolyzing)","type":"related"},{"name":"xanthosine 5'-phosphate amidotransferase activity","type":"related"},{"name":"xanthosine-5'-phosphate:L-glutamine amido-ligase (AMP-forming)","type":"related"}],"termid":"GO:0003922","terms_by_termid":{"GO:0003921":null,"GO:0003922":null}}


id: PBO:0046223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin C pseudogene 16","termid":"PBO:0046223"}


id: GO:0045636
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of melanocyte differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of melanocyte differentiation","termid":"GO:0045634"},{"relation_name":"is_a","term_name":"positive regulation of pigment cell differentiation","termid":"GO:0050942"},{"relation_name":"positively_regulates","term_name":"melanocyte differentiation","termid":"GO:0030318"}],"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 melanocyte differentiation","synonyms":[{"name":"activation of melanocyte differentiation","type":"narrow"},{"name":"positive regulation of melanophore differentiation","type":"exact"},{"name":"stimulation of melanocyte differentiation","type":"narrow"},{"name":"up regulation of melanocyte differentiation","type":"exact"},{"name":"up-regulation of melanocyte differentiation","type":"exact"},{"name":"upregulation of melanocyte differentiation","type":"exact"}],"termid":"GO:0045636"}


id: MONDO:0021488
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the lacrimal gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal gland neoplasm","termid":"MONDO:0021222"},{"relation_name":"is_a","term_name":"benign neoplasm of eye","termid":"MONDO:0021454"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"benign neoplasm of lacrimal gland","secondary_identifiers":["icd11.foundation:1163790602","SCTID:92169007","NCIT:C3621","UMLS:C0154024","MEDGEN:57813","ICD9:224.2"],"synonyms":[{"name":"benign lacrimal gland neoplasm","type":"exact"},{"name":"benign lacrimal gland tumor","type":"exact"},{"name":"benign lacrimal gland tumour","type":"exact"},{"name":"benign neoplasm of the lacrimal gland","type":"exact"},{"name":"benign tumor of lacrimal gland","type":"exact"},{"name":"benign tumor of the lacrimal gland","type":"exact"},{"name":"benign tumour of lacrimal gland","type":"exact"},{"name":"benign tumour of the lacrimal gland","type":"exact"},{"name":"lacrimal gland benign neoplasm","type":"exact"}],"termid":"MONDO:0021488","xrefs":{"Monarch":{"xref_id":"0021488"}}}


id: PR:Q10137
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spo20 gene.","definition_xrefs":["UniProtKB:Q10137","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":"sec14 cytosolic factor (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3H8.10","synonyms":[{"name":"PI/PC TP (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-spo20","type":"exact"},{"name":"phosphatidylinositol/phosphatidyl-choline transfer protein (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"sporulation-specific protein 20 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10137"}


id: MONDO:1012900
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any xanthinuria that occurs in dogs due to a mutation in the XDH gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"xanthinuria, dog","termid":"MONDO:1011623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"xanthinuria, XDH-related, dog","secondary_identifiers":["OMIA:002445-9615"],"synonyms":[{"name":"xanthinuria, type I, dog","type":"exact"}],"termid":"MONDO:1012900","xrefs":{"Monarch":{"xref_id":"1012900"}}}


id: PBO:0062554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily S member 24 pseudogene","termid":"PBO:0062554"}


id: MONDO:0020314
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete refractory anemia (obsolete MONDO:0020314)","termid":"MONDO:0020314","xrefs":{"Monarch":{"xref_id":"0020314"}}}


id: GO:0032636
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-7 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-7 production","secondary_identifiers":["GO:0042227","GO:0072605"],"synonyms":[{"name":"IL-7 production","type":"exact"},{"name":"interleukin-7 biosynthetic process","type":"narrow"},{"name":"interleukin-7 secretion","type":"narrow"}],"termid":"GO:0032636"}


id: FYPO:0003522
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of hercynylcysteine sulfoxide measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell","termid":"FYPO:0000990"}],"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 hercynylcysteine sulfoxide level","synonyms":[{"name":"increased cellular hercynylcysteine sulphoxide level","type":"exact"},{"name":"increased hercynylcysteine sulfoxide level","type":"exact"}],"termid":"FYPO:0003522"}


id: MONDO:1010931
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polymyositis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polymyositis, non-human animal","termid":"MONDO:1010203"},{"relation_name":"is_a","term_name":"myopathy, dog","termid":"MONDO:1010917"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polymyositis, dog","secondary_identifiers":["OMIA:001874-9615"],"termid":"MONDO:1010931","xrefs":{"Monarch":{"xref_id":"1010931"}}}


id: PBO:0087956
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transmembrane nucleoporin; involved in nuclear pore complex (NPC) distribution, assembly or stabilization; highly conserved across species, orthologous to human TMEM33 and paralogous to Per33p; protein abundance increases in response to DNA replication stress","termid":"PBO:0087956"}


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


id: MONDO:0003702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign neoplasm characterized by the presence of smooth muscle cells growing within the veins of the uterine corpus. The intravascular neoplasm growth occurs outside the confines of an adjacent leiomyoma.","definition_xrefs":["NCIT:C5356"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"uterine corpus diffuse leiomyomatosis","termid":"MONDO:0003704"},{"relation_name":"is_a","term_name":"uterine benign neoplasm","termid":"MONDO:0000632"},{"relation_name":"is_a","term_name":"intravenous leiomyomatosis","termid":"MONDO:0003614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterus intravascular leiomyomatosis","secondary_identifiers":["DOID:5915"],"synonyms":[{"name":"intravascular leiomyomatosis of the uterus","type":"exact"},{"name":"intravascular leiomyomatosis of uterus","type":"exact"},{"name":"intravenous leiomyomatosis of the uterus","type":"exact"},{"name":"intravenous leiomyomatosis of uterus","type":"exact"},{"name":"uterine corpus intravenous leiomyomatosis","type":"exact"},{"name":"uterus intravenous leiomyomatosis","type":"exact"}],"termid":"MONDO:0003702","xrefs":{"Monarch":{"xref_id":"0003702"}}}


id: MONDO:0016520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Klippel-Feil Syndrome is characterized by improper segmentation of cervical segments resulting in congenitally fused cervical vertebrae.","definition_xrefs":["Orphanet:2345"],"gene_count":0,"genotype_count":0,"name":"obsolete isolated Klippel-Feil syndrome (obsolete MONDO:0016520)","synonyms":[{"name":"Klippel-Feil malformation","type":"exact"},{"name":"Klippel-Feil sequence","type":"exact"},{"name":"congenital cervical vertebral fusion","type":"exact"},{"name":"congenital fused cervical segments","type":"exact"},{"name":"nonsyndromic Klippel-Feil syndrome","type":"exact"}],"termid":"MONDO:0016520","xrefs":{"Monarch":{"xref_id":"0016520"}}}


id: PBO:0081952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNRF3 intronic transcript 1","termid":"PBO:0081952"}


id: PBO:0038468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily A member 7","termid":"PBO:0038468"}


id: PBO:0059690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 56","termid":"PBO:0059690"}


id: GO:0001965
data:
  {"annotated_genes":["SJAG_02027"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74112],"is_not":false,"summary":null,"term":"GO:0001965"}]},"cv_name":"molecular_function","definition":"Binding to a G-protein alpha subunit. The alpha subunit binds a guanine nucleotide.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02027":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"G-protein alpha-subunit binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"G-alpha protein subunit binding","type":"exact"}],"termid":"GO:0001965","terms_by_termid":{"GO:0001965":null}}


id: MONDO:0000859
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The mildest form of spina bifida, characterized by any of several neural tube defects which may go undetected until an x-ray is performed. Treatment is symptomatic.","definition_xrefs":["NCIT:C101044"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spina bifida","termid":"MONDO:0008449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"spina bifida occulta","secondary_identifiers":["SCTID:76916001","icd11.foundation:449489594","ICD9:756.17","HP:0003298","DOID:0080073","MESH:D016136","UMLS:C0080174","GARD:10787","Orphanet:645202","MEDGEN:36380"],"synonyms":[{"name":"closed spinal dysraphism","type":"exact"},{"name":"spina bifida occulta","type":"exact"},{"name":"spina bifida occulta (disease)","type":"exact"}],"termid":"MONDO:0000859","xrefs":{"Monarch":{"xref_id":"0000859"}}}


id: MONDO:1011618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Waardenburg syndrome that occurs in golden hamster.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Waardenburg syndrome, non-human animal","termid":"MONDO:1011447"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Waardenburg syndrome, golden hamster","secondary_identifiers":["OMIA:001059-10036"],"termid":"MONDO:1011618","xrefs":{"Monarch":{"xref_id":"1011618"}}}


id: GO:0046426
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a receptor signaling pathway via JAK-STAT.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of receptor signaling pathway via JAK-STAT","termid":"GO:0046425"},{"relation_name":"is_a","term_name":"negative regulation of receptor signaling pathway via STAT","termid":"GO:1904893"},{"relation_name":"negatively_regulates","term_name":"cell surface receptor signaling pathway via JAK-STAT","termid":"GO:0007259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of receptor signaling pathway via JAK-STAT","secondary_identifiers":["GO:2000365"],"synonyms":[{"name":"down regulation of JAK-STAT cascade","type":"exact"},{"name":"down-regulation of JAK-STAT cascade","type":"exact"},{"name":"downregulation of JAK-STAT cascade","type":"exact"},{"name":"inhibition of JAK-STAT cascade","type":"narrow"},{"name":"negative regulation of STAT protein import into nucleus","type":"narrow"},{"name":"negative regulation of STAT protein nuclear translocation","type":"narrow"}],"termid":"GO:0046426"}


id: GO:0072733
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 staurosporine stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to alkaloid","termid":"GO:0043279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to staurosporine","termid":"GO:0072733"}


id: MONDO:0000142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete multiple congenital anomalies-hypotonia-seizures syndrome (obsolete MONDO:0000142)","termid":"MONDO:0000142","xrefs":{"Monarch":{"xref_id":"0000142"}}}


id: PBO:0056521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane bound transcription factor peptidase, site 1","termid":"PBO:0056521"}


id: PBO:0076218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-phase upregulated non-coding 1","termid":"PBO:0076218"}


id: PBO:0004326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smaug family","termid":"PBO:0004326"}


id: MONDO:0054813
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"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":"Ehlers-Danlos syndrome, classic-like, 2","secondary_identifiers":["Orphanet:536532","DOID:0080732","UMLS:C4693870","GARD:17975","OMIM:618000","MEDGEN:1632001"],"synonyms":[{"name":"EDSCLL2","type":"exact"},{"name":"Ehlers-Danlos syndrome, classic-like, 2","type":"exact"}],"termid":"MONDO:0054813","xrefs":{"Monarch":{"xref_id":"0054813"}}}


id: GO:0017158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of calcium ion-dependent exocytosis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of regulated secretory pathway","termid":"GO:1903305"},{"relation_name":"regulates","term_name":"calcium-ion regulated exocytosis","termid":"GO:0017156"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"regulation of calcium ion-dependent exocytosis","termid":"GO:0017158"}


id: GO:0002647
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of central tolerance induction.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of tolerance induction","termid":"GO:0002644"},{"relation_name":"is_a","term_name":"regulation of central tolerance induction","termid":"GO:0002646"},{"relation_name":"negatively_regulates","term_name":"central tolerance induction","termid":"GO:0002508"}],"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 central tolerance induction","synonyms":[{"name":"down regulation of central tolerance induction","type":"exact"},{"name":"down-regulation of central tolerance induction","type":"exact"},{"name":"downregulation of central tolerance induction","type":"exact"},{"name":"inhibition of central tolerance induction","type":"narrow"}],"termid":"GO:0002647"}


id: GO:0010986
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of lipoprotein particle clearance. Lipoprotein particle clearance is the process in which a lipoprotein particle is removed from the blood via receptor-mediated endocytosis and its constituent parts degraded.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lipoprotein particle clearance","termid":"GO:0010984"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"plasma lipoprotein particle clearance","termid":"GO:0034381"}],"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 lipoprotein particle clearance","termid":"GO:0010986"}


id: GO:0004923
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with leukemia inhibitory factor (LIF) and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:mah","GOC:signaling","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary neurotrophic factor receptor activity","termid":"GO:0004897"}],"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":"leukemia inhibitory factor receptor activity","secondary_identifiers":["GO:0004899"],"synonyms":[{"name":"LIF receptor activity","type":"exact"},{"name":"leukemia inhibitory factor receptor beta-protein activity","type":"narrow"}],"termid":"GO:0004923"}


id: GO:0045182
data:
  {"annotated_genes":["SJAG_03550","SJAG_04959","SJAG_04929","SJAG_02043","SJAG_01249","SJAG_05000","SJAG_00887","SJAG_01517"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103810,109214,101332,103196,90386,100584,102353,114644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008494"}]},"cv_name":"molecular_function","definition":"Any molecular function involved in the regulation of initiation, activation, perpetuation, repression or termination of polypeptide synthesis at the ribosome.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00887":null,"SJAG_01249":null,"SJAG_01517":null,"SJAG_02043":null,"SJAG_03550":null,"SJAG_04929":null,"SJAG_04959":null,"SJAG_05000":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"translation regulator activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0045182","terms_by_termid":{"GO:0008494":null}}


id: PBO:0042446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC42 effector protein 4","termid":"PBO:0042446"}


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


id: FYPO:0000974
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the cellular response to zinc ions is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular response to chemical stimulus during vegetative growth","termid":"FYPO:0001318"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000298","FYPO:0001312","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal cellular response to zinc ion","synonyms":[{"name":"normal cellular response to zinc","type":"exact"},{"name":"normal cellular response to zinc ion during mitotic cell cycle","type":"related"},{"name":"normal cellular response to zinc ion during vegetative growth","type":"exact"}],"termid":"FYPO:0000974"}


id: PBO:0084516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of conserved ER transmembrane complex; required for efficient folding of proteins in the ER; null mutant displays induction of the unfolded protein response; homologous to worm Y57G7A.10/EMC-2, fly CG17556, human TTC35","termid":"PBO:0084516"}


id: PBO:0045197
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 B8","termid":"PBO:0045197"}


id: GO:0043717
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-2-hydroxyglutaryl-CoA = H2O + glutaconyl-CoA.","definition_xrefs":["MetaCyc:RXN-1083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"2-hydroxyglutaryl-CoA dehydratase activity","secondary_identifiers":["RHEA:42448"],"synonyms":[{"name":"(R)-2-hydroxyglutaryl-CoA dehydratase activity","type":"exact"}],"termid":"GO:0043717"}


id: MONDO:0003384
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A clear cell adenocarcinoma of the uterine ligament composed mainly of clear or hobnob cells. The clear cells are large, bizarre, and multinucleated.","definition_xrefs":["NCIT:C40139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine ligament adenocarcinoma","termid":"MONDO:0002741"},{"relation_name":"is_a","term_name":"cervical clear cell adenocarcinoma","termid":"MONDO:0006135"}],"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":"uterine ligament clear cell adenocarcinoma","secondary_identifiers":["DOID:5302"],"synonyms":[{"name":"uterine ligament clear cell adenocarcinoma","type":"exact"}],"termid":"MONDO:0003384","xrefs":{"Monarch":{"xref_id":"0003384"}}}


id: GO:0009822
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of alkaloids, nitrogen containing natural products not otherwise classified as peptides, nonprotein amino acids, amines, cyanogenic glycosides, glucosinolates, cofactors, phytohormones or primary metabolites (such as purine or pyrimidine bases).","definition_xrefs":["ISBN:0122146743","GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"alkaloid metabolic process","termid":"GO:0009820"}],"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":"alkaloid catabolic process","synonyms":[{"name":"alkaloid breakdown","type":"exact"},{"name":"alkaloid catabolism","type":"exact"},{"name":"alkaloid degradation","type":"exact"}],"termid":"GO:0009822"}


id: PR:O74470
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1739.08c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74470"],"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 oxidoreductase C1739.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1739.08c","synonyms":[{"name":"Spom972h-SPCC1739.08c","type":"exact"}],"termid":"PR:O74470"}


id: MONDO:0019367
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Regional odontodysplasia (ROD) is a localized developmental anomaly of the dental tissues.","definition_xrefs":["Orphanet:83450"],"direct_ancestors":[{"relation_name":"is_a","term_name":"periodontal disorder","termid":"MONDO:0002635"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regional odontodysplasia","secondary_identifiers":["GARD:19036","icd11.foundation:1516505714","MEDGEN:104891","UMLS:C0206554","SCTID:66063001","MESH:D018126"],"synonyms":[{"name":"ghost teeth","type":"exact"}],"termid":"MONDO:0019367","xrefs":{"Monarch":{"xref_id":"0019367"}}}


id: MONDO:0010692
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":"nuclear ribonucleic acid","secondary_identifiers":["MEDGEN:374259","OMIM:310650","UMLS:C1839581"],"synonyms":[{"name":"nRNA","type":"related"},{"name":"nuclear ribonucleic acid","type":"exact"}],"termid":"MONDO:0010692","xrefs":{"Monarch":{"xref_id":"0010692"}}}


id: PBO:0058638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6769b","termid":"PBO:0058638"}


id: GO:0005334
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: norepinephrine(out) + Na+(out) + Cl-(out) = norepinephrine(in) + Na+(in) + Cl-(in).","definition_xrefs":["TC:2.A.22.1.2","PMID:21752877","PMID:22519513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoamine transmembrane transporter activity","termid":"GO:0008504"},{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"sodium:chloride symporter activity","termid":"GO:0015378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"norepinephrine:sodium symporter activity","secondary_identifiers":["Reactome:R-HSA-5659764","Wikipedia:Norepinephrine_transporter","Reactome:R-HSA-443997","GO:0005333"],"synonyms":[{"name":"levarterenol transporter activity","type":"exact"},{"name":"noradrenaline transporter activity","type":"exact"},{"name":"norepinephrine transmembrane transporter activity","type":"exact"},{"name":"norepinephrine:sodium:chloride symporter activity","type":"exact"},{"name":"sodium/norepinephrine symporter activity","type":"exact"}],"termid":"GO:0005334"}


id: PBO:0072805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterile alpha motif domain containing 1","termid":"PBO:0072805"}


id: PBO:0066695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RecQ mediated genome instability 1","termid":"PBO:0066695"}


id: PATO:0002514
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An orientation quality inhering in a bearer by virtue of the bearer having a position that is directed anteromedially.","definition_xrefs":["PATOC:EJS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orientation","termid":"PATO:0000133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anteromedial orientation","synonyms":[{"name":"medioanterior orientation","type":"exact"}],"termid":"PATO:0002514"}


id: GO:1903832
data:
  {"annotated_genes":["SJAG_02292","SJAG_02331"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68093,71088],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903833"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to amino acid starvation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:25002487","PMID:7623840"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to nutrient levels","termid":"GO:0032107"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"cellular response to amino acid starvation","termid":"GO:0034198"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02292":null,"SJAG_02331":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 cellular response to amino acid starvation","references_by_uniquename":{"GO_REF:0000117":null},"termid":"GO:1903832","terms_by_termid":{"GO:1903833":null}}


id: PBO:0064013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 47","termid":"PBO:0064013"}


id: PBO:0077525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 239","termid":"PBO:0077525"}


id: PBO:0004316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear rim protein Amo1","termid":"PBO:0004316"}


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


id: GO:0004465
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: triacylglycerol + H2O = diacylglycerol + a carboxylate, where the triacylglycerol is part of a lipoprotein. May also hydrolyze diacylglycerol and phospholipids present in lipoproteins.","definition_xrefs":["EC:3.1.1.34","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triacylglycerol lipase activity","termid":"GO:0004806"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"lipoprotein lipase activity","secondary_identifiers":["Reactome:R-HSA-8980228","Reactome:R-HSA-8979996","Reactome:R-HSA-6789310","Reactome:R-HSA-1482811","Reactome:R-HSA-174757","Reactome:R-HSA-2395768"],"synonyms":[{"name":"clearing factor lipase activity","type":"related"},{"name":"diacylglycerol hydrolase activity","type":"related"},{"name":"diacylglycerol lipase activity","type":"related"},{"name":"diglyceride lipase activity","type":"related"},{"name":"lipemia-clearing factor","type":"related"},{"name":"postheparin esterase activity","type":"related"},{"name":"postheparin lipase activity","type":"related"},{"name":"triacylglycero-protein acylhydrolase activity","type":"related"}],"termid":"GO:0004465"}


id: MONDO:0011028
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive limb-girdle muscular dystrophy type 2F (LGMD2F) is a subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuropsychomotor development is usually normal.","definition_xrefs":["Orphanet:219"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of delta-sarcoglycan","termid":"MONDO:0016144"},{"relation_name":"is_a","term_name":"familial dilated cardiomyopathy","termid":"MONDO:0016333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005267","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive limb-girdle muscular dystrophy type 2F","secondary_identifiers":["UMLS:C1832525","MEDGEN:331308","DOID:0110280","OMIM:601287","SCTID:718177001","MESH:C535896","GARD:8573"],"synonyms":[{"name":"LGMD2F","type":"exact"},{"name":"SGCD autosomal recessive limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCD","type":"exact"},{"name":"delta-sarcoglycanopathy","type":"broad"},{"name":"limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency","type":"exact"},{"name":"limb-girdle muscular dystrophy type 2F","type":"related"},{"name":"muscular dystrophy limb-girdle with delta-sarcoglyan deficiency","type":"related"},{"name":"muscular dystrophy, limb-girdle, autosomal recessive 6","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 2F","type":"related"}],"termid":"MONDO:0011028","xrefs":{"Monarch":{"xref_id":"0011028"}}}


id: GO:0071988
data:
  {"annotated_genes":["SJAG_01790","SJAG_04901","SJAG_03915","SJAG_05319","SJAG_01775","SJAG_00082","SJAG_03437","SJAG_02529","SJAG_01546","SJAG_01211","SJAG_01224","SJAG_01371","SJAG_00918","SJAG_05266","SJAG_02731","SJAG_05220"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061509"},{"annotations":[98745,93130,115907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902441"},{"annotations":[91827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902440"},{"annotations":[109439,110833,92810,116074,111844,90964,118904,98647,102412,91571,100500],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990976"}]},"cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained at, the spindle pole body.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to microtubule organizing center","termid":"GO:1905508"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01371":null,"SJAG_01546":null,"SJAG_01775":null,"SJAG_01790":null,"SJAG_02529":null,"SJAG_02731":null,"SJAG_03437":null,"SJAG_03915":null,"SJAG_04901":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05319":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to spindle pole body","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"protein localisation to spindle pole body","type":"exact"}],"termid":"GO:0071988","terms_by_termid":{"GO:0061509":null,"GO:1902440":null,"GO:1902441":null,"GO:1990976":null}}


id: PBO:0065233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 13 pseudogene 1","termid":"PBO:0065233"}


id: GO:0023037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a light signal causes activation of a receptor.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signal initiation by light (obsolete GO:0023037)","synonyms":[{"name":"signal initiation by light","type":"exact"}],"termid":"GO:0023037"}


id: GO:0015413
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + Ni2+(out) = ADP + phosphate + Ni2+(in).","definition_xrefs":["RHEA:15557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nickel cation transmembrane transporter activity","termid":"GO:0015099"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"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:0022857","GO:0005215"],"is_obsolete":false,"name":"ABC-type nickel transporter activity","secondary_identifiers":["GO:0102016","MetaCyc:ABC-20-RXN","EC:7.2.2.11"],"synonyms":[{"name":"ATP-dependent nickel transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled nickel transmembrane transporter activity","type":"related"},{"name":"nickel ABC transporter","type":"exact"},{"name":"nickel ABC transporter activity","type":"exact"},{"name":"nickel porter activity","type":"related"},{"name":"nickel transporting ATPase activity","type":"related"},{"name":"nickel-transporting ATPase activity","type":"related"}],"termid":"GO:0015413"}


id: PBO:0073109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short chain dehydrogenase/reductase family 16C member 5","termid":"PBO:0073109"}


id: MONDO:0002745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare borderline or malignant epithelial tumor of the fallopian tube characterized by the presence of neoplastic epithelial cells that contain intracytoplasmic mucin and may resemble the epithelial cells of the endocervix or gastrointestinal tract.","definition_xrefs":["NCIT:C40109"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube neoplasm","termid":"MONDO:0021092"},{"relation_name":"is_a","term_name":"mucinous neoplasm","termid":"MONDO:0024338"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fallopian tube mucinous tumor","secondary_identifiers":["DOID:3705","MEDGEN:275871","UMLS:C1517120"],"synonyms":[{"name":"fallopian tube mucinous neoplasm","type":"exact"},{"name":"fallopian tube mucinous tumor","type":"exact"}],"termid":"MONDO:0002745","xrefs":{"Monarch":{"xref_id":"0002745"}}}


id: PBO:0079984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP9Y pseudogene 22","termid":"PBO:0079984"}


id: PBO:0052542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kallikrein related peptidase 15","termid":"PBO:0052542"}


id: PBO:0090646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Slx9","termid":"PBO:0090646"}


id: PBO:0043711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 6A2","termid":"PBO:0043711"}


id: MONDO:0005082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from glandular epithelial cells of the prostate gland","direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"prostate carcinoma","termid":"MONDO:0005159"}],"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":"prostate adenocarcinoma","secondary_identifiers":["UMLS:C0007112","ONCOTREE:PRAD","EFO:0000673","NCIT:C2919","MEDGEN:764","SCTID:399490008","DOID:2526"],"synonyms":[{"name":"adenocarcinoma of prostate","type":"exact"},{"name":"adenocarcinoma of the prostate","type":"exact"},{"name":"prad","type":"related"},{"name":"prostate adenocarcinoma","type":"exact"},{"name":"prostate gland adenocarcinoma","type":"exact"}],"termid":"MONDO:0005082","xrefs":{"Monarch":{"xref_id":"0005082"}}}


id: SO:0001945
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 56th residue (a lysine), from the start of the H3 histone protein is acetylated.","definition_xrefs":["EBI:nj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_3_acetylation_site","termid":"SO:0001973"}],"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":"H3K56_acetylation_site","synonyms":[{"name":"H3K56 acetylation site","type":"exact"},{"name":"H3K56ac","type":"exact"}],"termid":"SO:0001945"}


id: PBO:0059617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ATP6 pseudogene 29","termid":"PBO:0059617"}


id: GO:0080026
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 indolebutyric acid stimulus.","definition_xrefs":["PMID:18725356"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to auxin","termid":"GO:0009733"},{"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 indolebutyric acid","synonyms":[{"name":"response to IBA stimulus","type":"exact"},{"name":"response to indole-3-butyric acid stimulus","type":"narrow"},{"name":"response to indolebutyric acid stimulus","type":"exact"}],"termid":"GO:0080026"}


id: MONDO:0000127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Geleophysic dysplasia is a rare skeletal dysplasia characterized by short stature, prominent abnormalities in hands and feet, and a characteristic facial appearance (described as \\\"happy'').","definition_xrefs":["Orphanet:2623"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acromelic dysplasia","termid":"MONDO:0019695"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"geleophysic dysplasia","secondary_identifiers":["GARD:2449","MEDGEN:483679","OMIMPS:231050","DOID:0111724","SCTID:28557005","MedDRA:10063361","UMLS:C3489726","icd11.foundation:518828851","ICD9:759.89"],"synonyms":[{"name":"geleophysic dwarfism","type":"exact"},{"name":"geleophysic dwarfism syndrome","type":"related"}],"termid":"MONDO:0000127","xrefs":{"Monarch":{"xref_id":"0000127"}}}


id: FYPO:0006576
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which abnormal negative regulation of the initiation of mitotic DNA replication results in one or more rounds of rereplication of the entire genome, and other features of S phase are abnormal. Rounds of replication are not correlated with G1/S phase gene expression, and origin usage is altered.","definition_xrefs":["PomBase:mah","PMID:20736315","PMID:19487461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal negative regulation of mitotic DNA replication initiation resulting in complete rereplication","termid":"FYPO:0001425"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000631","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal negative regulation of mitotic DNA replication initiation resulting in complete rereplication, with abnormal S phase","synonyms":[{"name":"abnormal negative regulation of DNA replication initiation resulting in complete rereplication, with abnormal S phase, during mitotic cell cycle","type":"related"},{"name":"abnormal negative regulation of mitotic DNA replication initiation resulting in complete rereplication, with abnormal S phase, during vegetative growth","type":"exact"},{"name":"abnormal negative regulation of mitotic DNA replication initiation resulting in continuous DNA synthesis","type":"related"}],"termid":"FYPO:0006576"}


id: GO:0140135
data:
  {"annotated_genes":["SJAG_02877","SJAG_05342","SJAG_05229","SJAG_04668","SJAG_02532"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105669],"is_not":false,"summary":null,"term":"GO:0140135"},{"annotations":[115901,94189,94247,101510],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015275"}]},"cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a monoatomic cation by a channel that opens in response to a mechanical stress.","definition_xrefs":["PMID:22343900","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic cation channel activity","termid":"GO:0005261"},{"relation_name":"is_a","term_name":"mechanosensitive monoatomic ion channel activity","termid":"GO:0008381"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02532":null,"SJAG_02877":null,"SJAG_04668":null,"SJAG_05229":null,"SJAG_05342":null},"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:0005215","GO:0003674"],"is_obsolete":false,"name":"mechanosensitive monoatomic cation channel activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9663363","Reactome:R-HSA-9855089","Reactome:R-HSA-9659380"],"synonyms":[{"name":"mechanically-gated cation channel activity","type":"exact"},{"name":"mechanosensitive cation channel activity","type":"broad"}],"termid":"GO:0140135","terms_by_termid":{"GO:0015275":null,"GO:0140135":null}}


id: GO:0150155
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-34 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:aruk","PMID:26754294"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-34 production","termid":"GO:0150155"}


id: PBO:0060221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAX dimerization protein 4","termid":"PBO:0060221"}


id: SO:0000216
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding glutaminyl tRNA (SO:0000260).","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamic_acid_tRNA_primary_transcript","synonyms":[{"name":"glutamic acid tRNA primary transcript","type":"exact"}],"termid":"SO:0000216"}


id: PBO:0005475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein Hsp20 family (predicted)","termid":"PBO:0005475"}


id: PBO:0110159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNAse Z, nuclear 3'-tRNA processing endonuclease Trz1","termid":"PBO:0110159"}


id: PBO:0049810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase 3","termid":"PBO:0049810"}


id: GO:2000088
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of mesonephric glomerulus development.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glomerulus development","termid":"GO:0090194"},{"relation_name":"is_a","term_name":"regulation of mesonephric glomerulus development","termid":"GO:2000087"},{"relation_name":"negatively_regulates","term_name":"mesonephric glomerulus development","termid":"GO:0061224"}],"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 mesonephric glomerulus development","termid":"GO:2000088"}


id: GO:0060400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of the growth hormone receptor signaling pathway. The growth hormone receptor signaling pathway is the series of molecular signals generated as a consequence of growth hormone receptor binding to its physiological ligand.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of growth hormone receptor signaling pathway","termid":"GO:0060398"},{"relation_name":"negatively_regulates","term_name":"growth hormone receptor signaling pathway","termid":"GO:0060396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of growth hormone receptor signaling pathway","synonyms":[{"name":"negative regulation of growth hormone receptor signalling pathway","type":"exact"}],"termid":"GO:0060400"}


id: MOD:00971
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:38"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Oxohistidine (from histidine)","termid":"MOD:00971"}


id: MONDO:0016639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lower limb malformation-hypospadias syndrome is a rare developmental defect during embryogenesis characterized by severe, uni- or bilateral lower limb malformations (incl. tibial hypoplasia, split and rocker bottom-shaped feet, and oligosyndactyly), normal upper limbs and hypospadias. Additional dysmorphic features (e.g. short neck and low-set, large ears), atrial septal defect, ureteropelvic junction stenosis and slight septation of the spleen, have also been reported. There have been no further descriptions in the literature since 1977.","definition_xrefs":["Orphanet:2487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lower limb deficiency-hypospadias syndrome","secondary_identifiers":["GARD:18773","MEDGEN:418952","MESH:C535640","UMLS:C2930962"],"synonyms":[{"name":"Fried-Goldberg-Mundel syndrome","type":"exact"},{"name":"lower limb malformation-hypospadias syndrome","type":"related"}],"termid":"MONDO:0016639","xrefs":{"Monarch":{"xref_id":"0016639"}}}


id: GO:0001134
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. The function of binding to an RNA polymerase (RNAP) transcription regulator and recruiting it to the general transcription machinery complex in order to modulate transcription initiation.","definition_xrefs":["GOC:txnOH-2018","PMID:16858867"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription regulator recruiting activity (obsolete GO:0001134)","synonyms":[{"name":"transcription factor activity, transcription factor recruiting","type":"related"},{"name":"transcription factor recruiting activity","type":"exact"},{"name":"transcription factor recruiting transcription factor activity","type":"exact"}],"termid":"GO:0001134"}


id: PBO:0081186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc fingers and homeoboxes 2","termid":"PBO:0081186"}


id: GO:1905723
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of trypanothione biosynthetic process.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:18949025"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"negative regulation of sulfur metabolic process","termid":"GO:0051175"},{"relation_name":"is_a","term_name":"regulation of trypanothione biosynthetic process","termid":"GO:1905722"},{"relation_name":"negatively_regulates","term_name":"trypanothione biosynthetic process","termid":"GO:0019342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0006790","GO:0008150"],"is_obsolete":false,"name":"negative regulation of trypanothione biosynthetic process","synonyms":[{"name":"down regulation of trypanothione anabolism","type":"exact"},{"name":"down regulation of trypanothione biosynthesis","type":"exact"},{"name":"down regulation of trypanothione biosynthetic process","type":"exact"},{"name":"down regulation of trypanothione formation","type":"exact"},{"name":"down regulation of trypanothione synthesis","type":"exact"},{"name":"down-regulation of trypanothione anabolism","type":"exact"},{"name":"down-regulation of trypanothione biosynthesis","type":"exact"},{"name":"down-regulation of trypanothione biosynthetic process","type":"exact"},{"name":"down-regulation of trypanothione formation","type":"exact"},{"name":"down-regulation of trypanothione synthesis","type":"exact"},{"name":"downregulation of trypanothione anabolism","type":"exact"},{"name":"downregulation of trypanothione biosynthesis","type":"exact"},{"name":"downregulation of trypanothione biosynthetic process","type":"exact"},{"name":"downregulation of trypanothione formation","type":"exact"},{"name":"downregulation of trypanothione synthesis","type":"exact"},{"name":"inhibition of trypanothione anabolism","type":"narrow"},{"name":"inhibition of trypanothione biosynthesis","type":"narrow"},{"name":"inhibition of trypanothione biosynthetic process","type":"narrow"},{"name":"inhibition of trypanothione formation","type":"narrow"},{"name":"inhibition of trypanothione synthesis","type":"narrow"},{"name":"negative regulation of trypanothione anabolism","type":"exact"},{"name":"negative regulation of trypanothione biosynthesis","type":"exact"},{"name":"negative regulation of trypanothione formation","type":"exact"},{"name":"negative regulation of trypanothione synthesis","type":"exact"}],"termid":"GO:1905723"}


id: MONDO:0016908
data:
  {"annotated_genes":["SJAG_00112"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014848"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 9","termid":"MONDO:0016874"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00112":null},"genotype_count":0,"is_obsolete":false,"name":"partial monosomy of the long arm of chromosome 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1051626600","UMLS:C5679677","MEDGEN:1826024","GARD:20829","Orphanet:262074"],"synonyms":[{"name":"partial deletion of chromosome 9q","type":"exact"},{"name":"partial deletion of the long arm of chromosome 9","type":"exact"},{"name":"partial monosomy of chromosome 9q","type":"exact"},{"name":"partial monosomy of the long arm of chromosome type 9","type":"exact"}],"termid":"MONDO:0016908","terms_by_termid":{"MONDO:0014848":null},"xrefs":{"Monarch":{"xref_id":"0016908"}}}


id: GO:0003256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter that contributes to the differentiation of a myocardial precursor cell.","definition_xrefs":["GOC:mtg_heart"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in myocardial precursor cell differentiation (obsolete GO:0003256)","termid":"GO:0003256"}


id: PBO:0029200
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_clotrimazole","termid":"PBO:0029200"}


id: PBO:0059941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 27","termid":"PBO:0059941"}


id: MONDO:0006026
data:
  {"annotated_genes":["SJAG_03453","SJAG_04277"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012672"},{"annotations":[88102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0001187"}]},"cv_name":"mondo","definition":"A disease involving the urinary bladder.","direct_ancestors":[{"relation_name":"is_a","term_name":"urinary system disorder","termid":"MONDO:0002118"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03453":null,"SJAG_04277":null},"genotype_count":0,"is_obsolete":false,"name":"urinary bladder disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:365","MESH:D001745","ICD9:596.8","EFO:1000018","SCTID:42643001","ICD9:596.9","MEDGEN:2278","NCIT:C2900","UMLS:C0005686"],"synonyms":[{"name":"bladder disease","type":"exact"},{"name":"bladder disorder","type":"exact"},{"name":"disease of urinary bladder","type":"exact"},{"name":"disease or disorder of urinary bladder","type":"exact"},{"name":"disorder of urinary bladder","type":"exact"},{"name":"urinary bladder disease","type":"exact"},{"name":"urinary bladder disease or disorder","type":"exact"},{"name":"urinary bladder disorder","type":"exact"}],"termid":"MONDO:0006026","terms_by_termid":{"MONDO:0001187":null,"MONDO:0012672":null},"xrefs":{"Monarch":{"xref_id":"0006026"}}}


id: PBO:0090757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphthamide synthetase Dph6","termid":"PBO:0090757"}


id: PBO:0075560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPG11 vesicle trafficking associated, spatacsin","termid":"PBO:0075560"}


id: SO:0001279
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"1,2'-O-dimethylinosine is a modified inosine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_inosine","termid":"SO:0001274"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"one_two_prime_O_dimethylinosine","secondary_identifiers":["RNAMOD:019"],"synonyms":[{"name":"1,2'-O-dimethylinosine","type":"exact"},{"name":"m'Im","type":"exact"},{"name":"one two prime O dimethylinosine","type":"exact"}],"termid":"SO:0001279"}


id: FYPO:0000430
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 fermentation is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular metabolism phenotype during vegetative growth","termid":"FYPO:0001348"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal fermentation","synonyms":[{"name":"abnormal fermentation during mitotic cell cycle","type":"related"},{"name":"abnormal fermentation during vegetative growth","type":"exact"},{"name":"abnormal fermentative metabolism","type":"exact"},{"name":"fermentative metabolism: abnormal","type":"related"}],"termid":"FYPO:0000430"}


id: FYPO:0006604
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 replication fork arrest at abnormal replication fork arrest at sites within the eukaryotic tRNA transcription unit occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal replication fork arrest","termid":"FYPO:0003088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000293"],"is_obsolete":false,"name":"decreased replication fork arrest at tRNA locus","synonyms":[{"name":"decreased replication fork arrest at tRNA genes","type":"exact"},{"name":"decreased replication fork arrest at tRNA locus during mitotic cell cycle","type":"related"},{"name":"decreased replication fork arrest at tRNA locus during vegetative growth","type":"exact"},{"name":"reduced replication fork arrest at tRNA locus","type":"exact"}],"termid":"FYPO:0006604"}


id: PBO:0040148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASH1 like histone lysine methyltransferase","termid":"PBO:0040148"}


id: MONDO:0015159
data:
  {"annotated_genes":["SJAG_00414","SJAG_00993","SJAG_01712","SJAG_03120","SJAG_05206","SJAG_01076","SJAG_02254","SJAG_01067","SJAG_04755","SJAG_04003","SJAG_04396","SJAG_02846","SJAG_01111","SJAG_00312","SJAG_02401","SJAG_02791","SJAG_00379","SJAG_05194","SJAG_01286","SJAG_03286","SJAG_04822","SJAG_01472","SJAG_02447","SJAG_04213","SJAG_02978","SJAG_04917","SJAG_03664","SJAG_02238","SJAG_03603","SJAG_02571","SJAG_03292","SJAG_01831","SJAG_04825","SJAG_02165","SJAG_00321","SJAG_03066","SJAG_00992","SJAG_04619","SJAG_05019","SJAG_02256","SJAG_02774","SJAG_00796","SJAG_02701","SJAG_04980","SJAG_00739","SJAG_03681","SJAG_00156","SJAG_03597","SJAG_03067","SJAG_00229","SJAG_04881","SJAG_04934","SJAG_01806","SJAG_00846","SJAG_03418","SJAG_03145","SJAG_01181","SJAG_04165","SJAG_04429","SJAG_01653","SJAG_03635","SJAG_02024","SJAG_03698","SJAG_04074","SJAG_01253","SJAG_01507","SJAG_01232","SJAG_02342","SJAG_01416","SJAG_03576","SJAG_00861","SJAG_03024","SJAG_03997","SJAG_04038","SJAG_04938","SJAG_02589","SJAG_03453","SJAG_05229","SJAG_04509","SJAG_03353","SJAG_04110","SJAG_02723","SJAG_02313","SJAG_00441","SJAG_04681","SJAG_01804","SJAG_01926","SJAG_01465","SJAG_00112","SJAG_03934","SJAG_01540","SJAG_05313"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012099"},{"annotations":[86833],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014700"},{"annotations":[87250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014558"},{"annotations":[87095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014601"},{"annotations":[88271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013812"},{"annotations":[88736],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010477"},{"annotations":[88348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011365"},{"annotations":[87390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008879"},{"annotations":[86842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014112"},{"annotations":[86845,86843,86844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014113"},{"annotations":[86848,86849,86850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014114"},{"annotations":[87212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014529"},{"annotations":[87082],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044701"},{"annotations":[86991],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010221"},{"annotations":[87972,87970,87971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013256"},{"annotations":[87794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007617"},{"annotations":[88516],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032912"},{"annotations":[87435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014838"},{"annotations":[87921,87922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032702"},{"annotations":[87103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014609"},{"annotations":[87299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012399"},{"annotations":[88598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011402"},{"annotations":[87361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007387"},{"annotations":[88843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010370"},{"annotations":[87501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012555"},{"annotations":[87959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013864"},{"annotations":[88066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957921"},{"annotations":[87006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009026"},{"annotations":[87929],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0034106"},{"annotations":[88794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032808"},{"annotations":[87737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013578"},{"annotations":[89005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044646"},{"annotations":[88743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007621"},{"annotations":[88222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011640"},{"annotations":[86900],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060627"},{"annotations":[87092,87091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014602"},{"annotations":[88764],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032787"},{"annotations":[87708,87707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026763"},{"annotations":[88805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030886"},{"annotations":[87098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014605"},{"annotations":[87730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024567"},{"annotations":[88521],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044319"},{"annotations":[88096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013819"},{"annotations":[88098,88097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013820"},{"annotations":[88099,88100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013821"},{"annotations":[87198,87197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030912"},{"annotations":[88436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014336"},{"annotations":[88046,88047],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011053"},{"annotations":[89061],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009622"},{"annotations":[87652,87653],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009479"},{"annotations":[87694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007843"},{"annotations":[88709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010465"},{"annotations":[87313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009514"},{"annotations":[87826,87825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014716"},{"annotations":[87718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014757"},{"annotations":[87789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012516"},{"annotations":[87474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014273"},{"annotations":[88647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015012"},{"annotations":[87779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013563"},{"annotations":[88708],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010466"},{"annotations":[87774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014165"},{"annotations":[87296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009736"},{"annotations":[88691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014466"},{"annotations":[87340],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060502"},{"annotations":[86883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009485"},{"annotations":[87710,87711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014751"},{"annotations":[87357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011213"},{"annotations":[87090,87089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060568"},{"annotations":[87934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014886"},{"annotations":[87626],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014238"},{"annotations":[87175],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054636"},{"annotations":[89030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010035"},{"annotations":[88692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010574"},{"annotations":[88868,88870,88869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010355"},{"annotations":[88485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010286"},{"annotations":[87444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014848"},{"annotations":[87927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014881"},{"annotations":[87455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014296"},{"annotations":[87978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009910"},{"annotations":[87421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008684"},{"annotations":[87072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010485"},{"annotations":[86869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010655"},{"annotations":[87958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010306"},{"annotations":[87123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010496"},{"annotations":[88984,88983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014936"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome","termid":"MONDO:0019042"}],"gene_count":92,"genes_by_uniquename":{"SJAG_00112":null,"SJAG_00156":null,"SJAG_00229":null,"SJAG_00312":null,"SJAG_00321":null,"SJAG_00379":null,"SJAG_00414":null,"SJAG_00441":null,"SJAG_00739":null,"SJAG_00796":null,"SJAG_00846":null,"SJAG_00861":null,"SJAG_00992":null,"SJAG_00993":null,"SJAG_01067":null,"SJAG_01076":null,"SJAG_01111":null,"SJAG_01181":null,"SJAG_01232":null,"SJAG_01253":null,"SJAG_01286":null,"SJAG_01416":null,"SJAG_01465":null,"SJAG_01472":null,"SJAG_01507":null,"SJAG_01540":null,"SJAG_01653":null,"SJAG_01712":null,"SJAG_01804":null,"SJAG_01806":null,"SJAG_01831":null,"SJAG_01926":null,"SJAG_02024":null,"SJAG_02165":null,"SJAG_02238":null,"SJAG_02254":null,"SJAG_02256":null,"SJAG_02313":null,"SJAG_02342":null,"SJAG_02401":null,"SJAG_02447":null,"SJAG_02571":null,"SJAG_02589":null,"SJAG_02701":null,"SJAG_02723":null,"SJAG_02774":null,"SJAG_02791":null,"SJAG_02846":null,"SJAG_02978":null,"SJAG_03024":null,"SJAG_03066":null,"SJAG_03067":null,"SJAG_03120":null,"SJAG_03145":null,"SJAG_03286":null,"SJAG_03292":null,"SJAG_03353":null,"SJAG_03418":null,"SJAG_03453":null,"SJAG_03576":null,"SJAG_03597":null,"SJAG_03603":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03681":null,"SJAG_03698":null,"SJAG_03934":null,"SJAG_03997":null,"SJAG_04003":null,"SJAG_04038":null,"SJAG_04074":null,"SJAG_04110":null,"SJAG_04165":null,"SJAG_04213":null,"SJAG_04396":null,"SJAG_04429":null,"SJAG_04509":null,"SJAG_04619":null,"SJAG_04681":null,"SJAG_04755":null,"SJAG_04822":null,"SJAG_04825":null,"SJAG_04881":null,"SJAG_04917":null,"SJAG_04934":null,"SJAG_04938":null,"SJAG_04980":null,"SJAG_05019":null,"SJAG_05194":null,"SJAG_05206":null,"SJAG_05229":null,"SJAG_05313":null},"genotype_count":0,"is_obsolete":false,"name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:19832","MEDGEN:1826158","Orphanet:102283","UMLS:C5680372"],"synonyms":[{"name":"MCA/MR","type":"exact"},{"name":"multiple congenital anomalies-intellectual disability with or without dysmorphism","type":"exact"},{"name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","type":"exact"}],"termid":"MONDO:0015159","terms_by_termid":{"MONDO:0007387":null,"MONDO:0007617":null,"MONDO:0007621":null,"MONDO:0007843":null,"MONDO:0008684":null,"MONDO:0008879":null,"MONDO:0009026":null,"MONDO:0009479":null,"MONDO:0009485":null,"MONDO:0009514":null,"MONDO:0009622":null,"MONDO:0009736":null,"MONDO:0009910":null,"MONDO:0010035":null,"MONDO:0010221":null,"MONDO:0010286":null,"MONDO:0010306":null,"MONDO:0010355":null,"MONDO:0010370":null,"MONDO:0010465":null,"MONDO:0010466":null,"MONDO:0010477":null,"MONDO:0010485":null,"MONDO:0010496":null,"MONDO:0010574":null,"MONDO:0010655":null,"MONDO:0011053":null,"MONDO:0011213":null,"MONDO:0011365":null,"MONDO:0011402":null,"MONDO:0011640":null,"MONDO:0012099":null,"MONDO:0012399":null,"MONDO:0012516":null,"MONDO:0012555":null,"MONDO:0013256":null,"MONDO:0013563":null,"MONDO:0013578":null,"MONDO:0013812":null,"MONDO:0013819":null,"MONDO:0013820":null,"MONDO:0013821":null,"MONDO:0013864":null,"MONDO:0014112":null,"MONDO:0014113":null,"MONDO:0014114":null,"MONDO:0014165":null,"MONDO:0014238":null,"MONDO:0014273":null,"MONDO:0014296":null,"MONDO:0014336":null,"MONDO:0014466":null,"MONDO:0014529":null,"MONDO:0014558":null,"MONDO:0014601":null,"MONDO:0014602":null,"MONDO:0014605":null,"MONDO:0014609":null,"MONDO:0014700":null,"MONDO:0014716":null,"MONDO:0014751":null,"MONDO:0014757":null,"MONDO:0014838":null,"MONDO:0014848":null,"MONDO:0014881":null,"MONDO:0014886":null,"MONDO:0014936":null,"MONDO:0015012":null,"MONDO:0024567":null,"MONDO:0026763":null,"MONDO:0030886":null,"MONDO:0030912":null,"MONDO:0032702":null,"MONDO:0032787":null,"MONDO:0032808":null,"MONDO:0032912":null,"MONDO:0034106":null,"MONDO:0044319":null,"MONDO:0044646":null,"MONDO:0044701":null,"MONDO:0054636":null,"MONDO:0060502":null,"MONDO:0060568":null,"MONDO:0060627":null,"MONDO:0957921":null},"xrefs":{"Monarch":{"xref_id":"0015159"}}}


id: PBO:0082344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent DNA translocase involved in chromatin remodeling; ATPase component that, with Itc1p, forms a complex required for repression of a-specific genes, INO1, and early meiotic genes during mitotic growth; exhibits basal levels of chromatin binding throughout the genome as well as interacts with sequence-specific factors to accurately position nucleosomes in chromatin; targeted by Ume6p- and Sua7p-dependent DNA looping to many loci genome-wide","termid":"PBO:0082344"}


id: PR:O94370
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1604.04 gene.","definition_xrefs":["UniProtKB:O94370","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized mitochondrial carrier C1604.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.04","synonyms":[{"name":"Spom972h-SPBC1604.04","type":"exact"}],"termid":"PR:O94370"}


id: GO:0120251
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a hydrocarbon, a compound consisting of carbon and hydrogen only.","definition_xrefs":["GOC:krc","Wikipedia:Hydrocarbon"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"hydrocarbon metabolic process","termid":"GO:0120252"}],"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":"hydrocarbon biosynthetic process","synonyms":[{"name":"hydrocarbon anabolism","type":"exact"},{"name":"hydrocarbon biosynthesis","type":"exact"},{"name":"hydrocarbon formation","type":"exact"},{"name":"hydrocarbon synthesis","type":"exact"}],"termid":"GO:0120251"}


id: PBO:0028768
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_nuclear_polyadenylated_mRNA_level_during_vegetative_growth","termid":"PBO:0028768"}


id: GO:0003021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which information about the levels of carbon dioxide are received and are converted to a molecular signal by chemoreceptors in the carotid bodies and the aortic bodies.","definition_xrefs":["ISBN:0323031951","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of carbon dioxide","termid":"GO:0003031"},{"relation_name":"part_of","term_name":"detection of hypoxic conditions in blood by chemoreceptor signaling","termid":"GO:0002007"}],"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 increased carbon dioxide by chemoreceptor signaling","synonyms":[{"name":"detection of increased carbon dioxide by chemoreceptor signalling","type":"exact"}],"termid":"GO:0003021"}


id: PBO:0117113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCG3 antisense RNA 1","termid":"PBO:0117113"}


id: GO:0018891
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving cyclohexanol, the monohydroxy derivative of cyclohexane. It is used as a solvent and blending agent.","definition_xrefs":["ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xenobiotic metabolic process","termid":"GO:0006805"},{"relation_name":"is_a","term_name":"secondary alcohol metabolic process","termid":"GO:1902652"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"cyclohexanol metabolic process","secondary_identifiers":["UM-BBD_pathwayID:chx"],"synonyms":[{"name":"cyclohexanol metabolism","type":"exact"}],"termid":"GO:0018891"}


id: PBO:0072657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retrotransposon Gag like 9","termid":"PBO:0072657"}


id: PBO:0039864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP26 intronic transcript 1","termid":"PBO:0039864"}


id: FYPO:0001938
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of cytochrome-c oxidase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased oxidoreductase activity","termid":"FYPO:0000690"},{"relation_name":"is_a","term_name":"abnormal cytochrome-c oxidase activity","termid":"FYPO:0001937"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0002114"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0005447","FYPO:0000138","FYPO:0002114","FYPO:0000707","FYPO:0001985","FYPO:0000002","FYPO:0000654"],"is_obsolete":false,"name":"decreased cytochrome-c oxidase activity","synonyms":[{"name":"reduced cytochrome-c oxidase activity","type":"exact"}],"termid":"FYPO:0001938"}


id: GO:0033865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a nucleoside bisphosphate, a compound consisting of a nucleobase linked to a deoxyribose or ribose sugar esterified with one phosphate group attached to each of two different hydroxyl groups on the sugar.","definition_xrefs":["GOC:pde","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside phosphate metabolic process","termid":"GO:0006753"}],"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:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"nucleoside bisphosphate metabolic process","synonyms":[{"name":"nucleoside bisphosphate metabolism","type":"exact"}],"termid":"GO:0033865"}


id: PBO:0040488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATXN7L3 antisense RNA 1","termid":"PBO:0040488"}


id: PBO:0084454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mannosylinositol phosphorylceramide (MIPC) synthase catalytic subunit; forms a complex with regulatory subunit Csg2p; function in sphingolipid biosynthesis is overlapping with that of Sur1p; CSH1 has a paralog, SUR1, that arose from the whole genome duplication","termid":"PBO:0084454"}


id: PBO:0043327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC like kinase 3 pseudogene 1","termid":"PBO:0043327"}


id: FYPO:0007380
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is longer than normal, and a new growth zone forms along the lateral portion of the cell (often in the middle) before septation, such that a single cell grows in the form of the letter T.","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated vegetative cell","termid":"FYPO:0001122"},{"relation_name":"is_a","term_name":"T-shaped vegetative cell","termid":"FYPO:0007379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005568"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000004","FYPO:0005568","FYPO:0000002","FYPO:0005447","FYPO:0000005","FYPO:0001985"],"is_obsolete":false,"name":"elongated T-shaped vegetative cell","synonyms":[{"name":"elongated T-shaped cell during vegetative growth","type":"exact"},{"name":"elongated T-shaped vegetative cell during mitotic cell cycle","type":"related"},{"name":"long T-shaped vegetative cell","type":"exact"}],"termid":"FYPO:0007380"}


id: MONDO:0023161
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myocarditis that is caused by an infection with a viral agent.","definition_xrefs":["NCIT:C128381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myocarditis","termid":"MONDO:0004496"},{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"viral myocarditis","secondary_identifiers":["icd11.foundation:231270764","SCTID:89141000","UMLS:C0276138","MEDGEN:547112"],"synonyms":[{"name":"Viral Myocarditis","type":"related"},{"name":"Viral myocarditis","type":"related"},{"name":"viral myocarditis","type":"exact"}],"termid":"MONDO:0023161","xrefs":{"Monarch":{"xref_id":"0023161"}}}


id: RO:HOM0000051
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Paedomorphosis that is produced by delayed growth of immature structures into the adult form.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_paedomorphorsis_relationship_with","termid":"RO:HOM0000029"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_postdisplacement_relationship_with","synonyms":[{"name":"post-displacement","type":"exact"}],"termid":"RO:HOM0000051"}


id: MOD:01704
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue to dehydrobutyrine, by neutral loss of methyl sulfide.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"},{"relation_name":"is_a","term_name":"dehydrobutyrine","termid":"MOD:01703"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrobutyrine (Met)","synonyms":[{"name":"dHAbu(Met)","type":"exact"}],"termid":"MOD:01704"}


id: GO:0060213
data:
  {"annotated_genes":["SJAG_01436","SJAG_00686","SJAG_04682"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74489,91522,106835],"is_not":false,"summary":null,"term":"GO:0060213"}]},"cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of poly(A) tail shortening of a nuclear-transcribed mRNA. Poly(A) tail shortening is the decrease in length of the poly(A) tail of an mRNA from full length to an oligo(A) length.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nuclear-transcribed mRNA poly(A) tail shortening","termid":"GO:0060211"},{"relation_name":"is_a","term_name":"positive regulation of mRNA catabolic process","termid":"GO:0061014"},{"relation_name":"positively_regulates","term_name":"nuclear-transcribed mRNA poly(A) tail shortening","termid":"GO:0000289"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00686":null,"SJAG_01436":null,"SJAG_04682":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0016071","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of nuclear-transcribed mRNA poly(A) tail shortening","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"positive regulation of 3' to 5' mRNA deadenylation","type":"related"},{"name":"positive regulation of mRNA deadenylation","type":"related"},{"name":"positive regulation of nuclear mRNA poly(A) tail shortening","type":"related"}],"termid":"GO:0060213","terms_by_termid":{"GO:0060213":null}}


id: PBO:0064583
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 D","termid":"PBO:0064583"}


id: FYPO:0004952
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the prospore membrane begins to form and enclose the nucleus, but the leading edge does not close completely, leaving a gap in the membrane.","definition_xrefs":["PMID:17951524","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal prospore membrane formation","termid":"FYPO:0001914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0000121"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000121"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000121","FYPO:0000002","FYPO:0000631"],"is_obsolete":false,"name":"incomplete prospore membrane closure","synonyms":[{"name":"incomplete enclosure of nucleus by forespore membrane","type":"related"},{"name":"incomplete engulfment of nucleus by forespore membrane","type":"related"},{"name":"incomplete forespore membrane closure","type":"exact"}],"termid":"FYPO:0004952"}


id: GO:0097135
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of cyclin E2 and cyclin-dependent kinase 2 (CDK2). Cyclins are characterized by periodicity in protein abundance throughout the cell cycle. Cyclin-dependent kinases represent a family of serine/threonine protein kinases that become active upon binding to a cyclin regulatory partner.","definition_xrefs":["PMID:15935619","GOC:so"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclin-dependent protein kinase holoenzyme complex","termid":"GO:0000307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"cyclin E2-CDK2 complex","termid":"GO:0097135"}


id: PR:P50582
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hsk1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P50582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell cycle serine/threonine-protein kinase hsk1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC776.12c","synonyms":[{"name":"Spom972h-hsk1","type":"exact"},{"name":"cdc7-related kinase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"minichromosome maintenance protein kinase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P50582"}


id: GO:0052100
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which single-celled organisms of the same species monitor population density by detecting the concentration of small, diffusible signal molecules.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete intraspecies quorum sensing (obsolete GO:0052100)","termid":"GO:0052100"}


id: GO:0070236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of activation-induced cell death of T cells.","definition_xrefs":["ISBN:0781765196","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of immune system process","termid":"GO:0002683"},{"relation_name":"is_a","term_name":"negative regulation of T cell apoptotic process","termid":"GO:0070233"},{"relation_name":"is_a","term_name":"regulation of activation-induced cell death of T cells","termid":"GO:0070235"},{"relation_name":"negatively_regulates","term_name":"activation-induced cell death of T cells","termid":"GO:0006924"}],"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 activation-induced cell death of T cells","synonyms":[{"name":"down regulation of activation-induced cell death of T cells","type":"exact"},{"name":"down-regulation of activation-induced cell death of T cells","type":"exact"},{"name":"downregulation of activation-induced cell death of T cells","type":"exact"},{"name":"inhibition of activation-induced cell death of T cells","type":"narrow"},{"name":"negative regulation of AICD","type":"broad"},{"name":"negative regulation of activated T cell apoptosis","type":"broad"},{"name":"negative regulation of activation-induced cell death of T lymphocytes","type":"exact"},{"name":"negative regulation of activation-induced cell death of T-cells","type":"exact"},{"name":"negative regulation of activation-induced cell death of T-lymphocytes","type":"exact"},{"name":"negative regulation of antigen-driven apoptosis","type":"broad"}],"termid":"GO:0070236"}


id: PBO:0086587
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; epitope-tagged protein localizes to the cytoplasm; YHR033W has a paralog, PRO1, that arose from the whole genome duplication","termid":"PBO:0086587"}


id: MONDO:0017212
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"choroiditis","termid":"MONDO:0001280"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"paraneoplastic uveitis","secondary_identifiers":["GARD:21069","Orphanet:279928","MEDGEN:1830109","UMLS:C5680786"],"termid":"MONDO:0017212","xrefs":{"Monarch":{"xref_id":"0017212"}}}


id: GO:1990392
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A trimeric cell-cell fusion complex that serves as a scaffold for zippering up the extracellular domains, bringing the transmembrane segments into close proximity such that they can continue zippering within the two membranes into one. Two prefusion monomers cluster at the surface of adjacent cells. Parallel EFF-1 interactions occur across cells and a third monomer, which can come from either cell, adds on to make an intermediate, extended trimer.","definition_xrefs":["PMID:24725407","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"EFF-1 complex","termid":"GO:1990392"}


id: GO:0030431
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an organism enters and maintains a periodic, readily reversible state of reduced awareness and metabolic activity. Usually accompanied by physical relaxation, the onset of sleep in humans and other mammals is marked by a change in the electrical activity of the brain.","definition_xrefs":["ISBN:0192800981"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"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":"sleep","secondary_identifiers":["Wikipedia:Sleep"],"synonyms":[{"name":"diapause","type":"related"},{"name":"dormancy","type":"related"},{"name":"lethargus","type":"related"}],"termid":"GO:0030431"}


id: GO:1901997
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of indoleacetic acid biosynthetic process via tryptophan.","definition_xrefs":["GOC:TermGenie","PMID:23377040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hormone biosynthetic process","termid":"GO:0032353"},{"relation_name":"is_a","term_name":"negative regulation of amine metabolic process","termid":"GO:0033239"},{"relation_name":"is_a","term_name":"negative regulation of amino acid metabolic process","termid":"GO:0045763"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"negative regulation of auxin metabolic process","termid":"GO:0090356"},{"relation_name":"is_a","term_name":"regulation of indoleacetic acid biosynthetic process via tryptophan","termid":"GO:1901996"},{"relation_name":"negatively_regulates","term_name":"indoleacetic acid biosynthetic process via tryptophan","termid":"GO:0009848"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"negative regulation of indoleacetic acid biosynthetic process via tryptophan","synonyms":[{"name":"down regulation of IAA biosynthetic process via tryptophan","type":"exact"},{"name":"down regulation of indoleacetic acid anabolism via tryptophan","type":"exact"},{"name":"down regulation of indoleacetic acid biosynthetic process via tryptophan","type":"exact"},{"name":"down regulation of indoleacetic acid formation via tryptophan","type":"exact"},{"name":"down regulation of indoleacetic acid synthesis via tryptophan","type":"exact"},{"name":"down-regulation of IAA biosynthetic process via tryptophan","type":"exact"},{"name":"down-regulation of indoleacetic acid anabolism via tryptophan","type":"exact"},{"name":"down-regulation of indoleacetic acid biosynthetic process via tryptophan","type":"exact"},{"name":"down-regulation of indoleacetic acid formation via tryptophan","type":"exact"},{"name":"down-regulation of indoleacetic acid synthesis via tryptophan","type":"exact"},{"name":"downregulation of IAA biosynthetic process via tryptophan","type":"exact"},{"name":"downregulation of indoleacetic acid anabolism via tryptophan","type":"exact"},{"name":"downregulation of indoleacetic acid biosynthetic process via tryptophan","type":"exact"},{"name":"downregulation of indoleacetic acid formation via tryptophan","type":"exact"},{"name":"downregulation of indoleacetic acid synthesis via tryptophan","type":"exact"},{"name":"inhibition of IAA biosynthetic process via tryptophan","type":"exact"},{"name":"inhibition of indoleacetic acid anabolism via tryptophan","type":"exact"},{"name":"inhibition of indoleacetic acid biosynthetic process via tryptophan","type":"narrow"},{"name":"inhibition of indoleacetic acid formation via tryptophan","type":"exact"},{"name":"inhibition of indoleacetic acid synthesis via tryptophan","type":"exact"},{"name":"negative regulation of IAA biosynthetic process via tryptophan","type":"exact"},{"name":"negative regulation of indoleacetic acid anabolism via tryptophan","type":"exact"},{"name":"negative regulation of indoleacetic acid formation via tryptophan","type":"exact"},{"name":"negative regulation of indoleacetic acid synthesis via tryptophan","type":"exact"}],"termid":"GO:1901997"}


id: PBO:0065564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostaglandin E synthase 3 pseudogene 4","termid":"PBO:0065564"}


id: MONDO:0005219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibrosis associated with cyst formation in the breast parenchyma.","definition_xrefs":["NCIT:C3039"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"breast disorder","termid":"MONDO:0002657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast fibrocystic disease","secondary_identifiers":["DOID:10354","MESH:D005348","UMLS:C0016034","MEDGEN:42015","ICD9:610.1","EFO:0003014"],"synonyms":[{"name":"benign breast disease","type":"exact"},{"name":"breast fibrocystic change","type":"exact"},{"name":"cystic disease of breast","type":"exact"},{"name":"cystic disease of the breast","type":"exact"},{"name":"diffuse cystic mastopathy","type":"exact"},{"name":"fibrocystic breast","type":"exact"},{"name":"fibrocystic breast changes","type":"exact"},{"name":"fibrocystic breast disease","type":"exact"},{"name":"fibrocystic change of breast","type":"exact"},{"name":"fibrocystic change of the breast","type":"exact"},{"name":"fibrocystic disease","type":"exact"},{"name":"fibrocystic disease of breast","type":"exact"},{"name":"fibrocystic disease of the breast","type":"exact"},{"name":"fibrocystic mastopathy","type":"exact"},{"name":"mammary dysplasia","type":"exact"}],"termid":"MONDO:0005219","xrefs":{"Monarch":{"xref_id":"0005219"}}}


id: GO:0019330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving aldoximes, compounds derived by the reaction of an aldose with hydroxylamine, thus containing the aldoxime group -HC=NOH.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"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":"aldoxime metabolic process","secondary_identifiers":["MetaCyc:P345-PWY"],"synonyms":[{"name":"aldoxime metabolism","type":"exact"}],"termid":"GO:0019330"}


id: PATO:0002308
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A triangular quality inhering in a bearer by virtue of the bearer's having all sides of unequal length.","definition_xrefs":["PATOC:JB"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triangular","termid":"PATO:0001875"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scalene triangular","termid":"PATO:0002308"}


id: PBO:0043668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coenzyme Q10B","termid":"PBO:0043668"}


id: MONDO:0012049
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"orofaciodigital syndrome","termid":"MONDO:0015375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"orofaciodigital syndrome VII","secondary_identifiers":["OMIM:608518","DOID:0060377","MESH:C563104","MEDGEN:162907","Orphanet:90649","UMLS:C0796100"],"synonyms":[{"name":"OFD7","type":"exact"},{"name":"Ofds 7","type":"related"},{"name":"Whelan syndrome","type":"exact"},{"name":"oral-Facial-digital syndrome, type 7","type":"related"},{"name":"orofaciodigital syndrome 7","type":"related"},{"name":"orofaciodigital syndrome VII","type":"exact"},{"name":"orofaciodigital syndrome type 7","type":"exact"},{"name":"orofaciodigital syndrome type VII","type":"exact"}],"termid":"MONDO:0012049","xrefs":{"Monarch":{"xref_id":"0012049"}}}


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


id: PBO:0090513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycosyltransferase 34 family","termid":"PBO:0090513"}


id: GO:1902836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of proline import into cell.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:24344203"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organic acid transport","termid":"GO:0032892"},{"relation_name":"is_a","term_name":"positive regulation of transmembrane transport","termid":"GO:0034764"},{"relation_name":"is_a","term_name":"positive regulation of amino acid transport","termid":"GO:0051957"},{"relation_name":"is_a","term_name":"regulation of proline import across plasma membrane","termid":"GO:1902834"},{"relation_name":"positively_regulates","term_name":"proline import across plasma membrane","termid":"GO:1905647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of proline import across plasma membrane","synonyms":[{"name":"activation of proline import into cell","type":"narrow"},{"name":"positive regulation of proline import into cell","type":"exact"},{"name":"up regulation of proline import into cell","type":"exact"},{"name":"up-regulation of proline import into cell","type":"exact"},{"name":"upregulation of proline import into cell","type":"exact"}],"termid":"GO:1902836"}


id: GO:0002579
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antigen processing and presentation","termid":"GO:0002577"},{"relation_name":"is_a","term_name":"positive regulation of immune system process","termid":"GO:0002684"},{"relation_name":"positively_regulates","term_name":"antigen processing and presentation","termid":"GO:0019882"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of antigen processing and presentation","synonyms":[{"name":"activation of antigen processing and presentation","type":"narrow"},{"name":"stimulation of antigen processing and presentation","type":"narrow"},{"name":"up regulation of antigen processing and presentation","type":"exact"},{"name":"up-regulation of antigen processing and presentation","type":"exact"},{"name":"upregulation of antigen processing and presentation","type":"exact"}],"termid":"GO:0002579"}


id: PBO:0089320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HECT-type ubiquitin-protein ligase E3, implicated in negative regulation of ubiquitinated chromatin formation","termid":"PBO:0089320"}


id: FYPO:0001713
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 malate into the cell is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal malate import","synonyms":[{"name":"abnormal malate import across plasma membrane","type":"exact"},{"name":"abnormal malate import during mitotic cell cycle","type":"related"},{"name":"abnormal malate import during vegetative growth","type":"exact"},{"name":"abnormal malate import into cell","type":"exact"},{"name":"abnormal malate uptake","type":"exact"},{"name":"abnormal malic acid import","type":"related"}],"termid":"FYPO:0001713"}


id: PR:O13717
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC14C4.10c gene.","definition_xrefs":["UniProtKB:O13717","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C14C4.10c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC14C4.10c","synonyms":[{"name":"Spom972h-SPAC14C4.10c","type":"exact"}],"termid":"PR:O13717"}


id: MONDO:0044279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bone mineral density quantitative trait locus 15 (obsolete MONDO:0044279)","secondary_identifiers":["OMIM:613418"],"synonyms":[{"name":"BMND15","type":"related"},{"name":"bone mineral density QTL 15","type":"exact"},{"name":"bone mineral density quantitative trait locus 15","type":"related"},{"name":"compression fracture, susceptibility to","type":"related"},{"name":"metaphyseal fracture, susceptibility to","type":"related"},{"name":"osteoporosis, susceptibility to","type":"related"}],"termid":"MONDO:0044279","xrefs":{"Monarch":{"xref_id":"0044279"}}}


id: PBO:0049209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate ionotropic receptor NMDA type subunit 2C","termid":"PBO:0049209"}


id: PBO:0060799
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit S5 pseudogene 5","termid":"PBO:0060799"}


id: PBO:0064833
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 pseudogene 1","termid":"PBO:0064833"}


id: GO:0035845
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level and results in the assembly, arrangement of constituent parts, or disassembly of the outer segment of a photoreceptor cell, a sensory cell that reacts to the presence of light. The outer segment of the photoreceptor cell contains the light-absorbing materials.","definition_xrefs":["ISBN:0824072820","PMID:14507858"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component organization","termid":"GO:0016043"},{"relation_name":"part_of","term_name":"photoreceptor cell development","termid":"GO:0042461"}],"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":"photoreceptor cell outer segment organization","synonyms":[{"name":"photoreceptor cell outer segment organisation","type":"exact"},{"name":"photoreceptor outer segment organization","type":"exact"}],"termid":"GO:0035845"}


id: GO:1990892
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which chromosome arm chromatin structure is compacted prior to and during mitosis in eukaryotic cells.","definition_xrefs":["PMID:21633354"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic chromosome condensation","termid":"GO:0007076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000070"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0000070","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"mitotic chromosome arm condensation","termid":"GO:1990892"}


id: PBO:0087419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit 8 of ubiquinol cytochrome-c reductase (Complex III); Complex III is a component of the mitochondrial inner membrane electron transport chain; oriented facing the intermembrane space; expression is regulated by Abf1p and Cpf1p","termid":"PBO:0087419"}


id: GO:0045507
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-25 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":"interleukin-17 receptor activity","termid":"GO:0030368"}],"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":"interleukin-25 receptor activity","synonyms":[{"name":"IL-25 receptor activity","type":"exact"},{"name":"IL-25R","type":"exact"}],"termid":"GO:0045507"}


id: PBO:0043168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cartilage intermediate layer protein","termid":"PBO:0043168"}


id: GO:0110078
data:
  {"annotated_genes":["SJAG_05206","SJAG_03267","SJAG_04784","SJAG_00112"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89285,99439,105621,119730],"is_not":false,"summary":null,"term":"GO:0110078"}]},"cv_name":"cellular_component","definition":"A Hsp90 cochaperone complex acting as an adapter between Hps90 and its substrates, members of the PIKK kinase family.","definition_xrefs":["PMID:22505622","PMID:20810650","PMID:28827813","PMID:34233195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00112":null,"SJAG_03267":null,"SJAG_04784":null,"SJAG_05206":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"TTT Hsp90 cochaperone complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"TELO2-TTI1-TTI2","type":"exact"},{"name":"TTT complex","type":"exact"},{"name":"Tel2-Tti1-Tti2","type":"exact"},{"name":"Triple T complex","type":"exact"}],"termid":"GO:0110078","terms_by_termid":{"GO:0110078":null}}


id: PBO:0113276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane protein of unknown function; targeted to vacuole via AP-3 pathway; truncation and overexpression suppresses lethality of G-alpha protein deficiency","termid":"PBO:0113276"}


id: PBO:0065663
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase receptor type M","termid":"PBO:0065663"}


id: PBO:0043476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2',3'-cyclic nucleotide 3' phosphodiesterase","termid":"PBO:0043476"}


id: PBO:0048646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gap junction protein beta 6","termid":"PBO:0048646"}


id: GO:0034360
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A lipoprotein particle that is derived from a mature chylomicron particle by the removal of triglycerides from the chylomicron core by lipoprotein lipase and the subsequent loss of surface components. It characteristically contains apolipoprotein E (APOE) and is cleared from the blood by the liver.","definition_xrefs":["GOC:expert_pt","GOC:BHF","GOC:mah","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chylomicron","termid":"GO:0042627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005576"],"is_obsolete":false,"name":"chylomicron remnant","termid":"GO:0034360"}


id: PBO:0067548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 697, pseudogene","termid":"PBO:0067548"}


id: MONDO:0012167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial atrial fibrillation","termid":"MONDO:0018054"}],"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":"atrial fibrillation, familial, 2","secondary_identifiers":["GARD:15446","MESH:C563903","OMIM:608988","MEDGEN:324886","UMLS:C1837812"],"synonyms":[{"name":"ATFB2","type":"exact"},{"name":"atrial fibrillation, familial, 2","type":"exact"}],"termid":"MONDO:0012167","xrefs":{"Monarch":{"xref_id":"0012167"}}}


id: GO:0070062
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A vesicle that is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane. Extracellular exosomes, also simply called exosomes, have a diameter of about 40-100 nm.","definition_xrefs":["PMID:22418571","PMID:15908444","PMID:24009894","PMID:17641064","GOC:BHF","PMID:19442504","GOC:mah","PMID:19498381","GOC:vesicles"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular vesicle","termid":"GO:1903561"},{"relation_name":"part_of","term_name":"extracellular space","termid":"GO:0005615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005575","GO:0005576"],"is_obsolete":false,"name":"extracellular exosome","synonyms":[{"name":"exosome","type":"exact"},{"name":"extracellular vesicular exosome","type":"exact"}],"termid":"GO:0070062"}


id: MONDO:0035075
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete secondary early-onset glaucoma of genetic origin (obsolete MONDO:0035075)","secondary_identifiers":["Orphanet:522580"],"termid":"MONDO:0035075","xrefs":{"Monarch":{"xref_id":"0035075"}}}


id: GO:0062045
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-lysine + pyruvate= epsilon-amino-alpha-ketocaproic acid (KAC) + alanine.","definition_xrefs":["PMID:27758894","PMID:28330936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016769"}],"interesting_parent_ids":["GO:0016769","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"L-lysine alpha-aminotransferase","termid":"GO:0062045"}


id: GO:1900727
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of osmoregulated periplasmic glucan.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucan biosynthetic process","termid":"GO:0009250"},{"relation_name":"is_a","term_name":"osmoregulated periplasmic glucan metabolic process","termid":"GO:1900725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"osmoregulated periplasmic glucan biosynthetic process","synonyms":[{"name":"osmoregulated periplasmic glucan anabolism","type":"exact"},{"name":"osmoregulated periplasmic glucan biosynthesis","type":"exact"},{"name":"osmoregulated periplasmic glucan formation","type":"exact"},{"name":"osmoregulated periplasmic glucan synthesis","type":"exact"}],"termid":"GO:1900727"}


id: MONDO:0006066
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A variant of acinar prostate adenocarcinoma characterized by the presence of malignant cells with abundant xanthomatous appearing cytoplasm.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostatic acinar adenocarcinoma","termid":"MONDO:0002493"}],"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":"acinar prostate adenocarcinoma, foamy gland variant","secondary_identifiers":["UMLS:C5787290","MEDGEN:1835068","NCIT:C39882","EFO:1000064"],"termid":"MONDO:0006066","xrefs":{"Monarch":{"xref_id":"0006066"}}}


id: GO:0021728
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the inferior reticular formation over time, from its formation to the mature structure.","definition_xrefs":["GOC:dgh","GOC:dph","GOC:curators","GO_REF:0000021","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"medullary reticular formation development","termid":"GO:0021723"}],"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":"inferior reticular formation development","termid":"GO:0021728"}


id: MONDO:0016935
data:
  {"annotated_genes":["SJAG_02231"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012574"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal duplication","termid":"MONDO:0000762"},{"relation_name":"is_a","term_name":"chromosome 17 disorder","termid":"MONDO:0020583"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02231":null},"genotype_count":0,"is_obsolete":false,"name":"partial duplication of chromosome 17","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:20855","Orphanet:262677","MEDGEN:1387434","SCTID:726356000","UMLS:C4518505"],"synonyms":[{"name":"partial duplication of chromosome type 17","type":"exact"},{"name":"partial trisomy of chromosome 17","type":"exact"}],"termid":"MONDO:0016935","terms_by_termid":{"MONDO:0012574":null},"xrefs":{"Monarch":{"xref_id":"0016935"}}}


id: FYPO:0005546
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to another occurs to a lower extent than normal during S phase of the mitotic cell cycle. The relevant proteins may include the one encoded by the mutated gene, or may both be encoded by different genes.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein-protein interaction","termid":"FYPO:0001645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000702"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0000702"],"is_obsolete":false,"name":"decreased protein-protein interaction during mitotic S phase","synonyms":[{"name":"decreased protein binding during mitotic S phase","type":"exact"},{"name":"reduced protein-protein interaction during mitotic S phase","type":"exact"}],"termid":"FYPO:0005546"}


id: MONDO:0001898
data:
  {"annotated_genes":["SJAG_02063","SJAG_00495"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010557"},{"annotations":[88874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009796"}]},"cv_name":"mondo","definition":"A disease involving the optic choroid.","direct_ancestors":[{"relation_name":"is_a","term_name":"uveal disorder","termid":"MONDO:0002661"},{"relation_name":"is_a","term_name":"ocular vascular disorder","termid":"MONDO:0005552"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00495":null,"SJAG_02063":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"optic choroid disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:892839","NCIT:C34468","DOID:1417","ICD9:363.8","ICD9:363.9","MESH:D015862","UMLS:C4025836","SCTID:128468007"],"synonyms":[{"name":"choroid disease","type":"related"},{"name":"choroid disorder","type":"exact"},{"name":"disease of optic choroid","type":"exact"},{"name":"disease or disorder of optic choroid","type":"exact"},{"name":"disorder of optic choroid","type":"exact"},{"name":"optic choroid disease","type":"exact"},{"name":"optic choroid disease or disorder","type":"exact"}],"termid":"MONDO:0001898","terms_by_termid":{"MONDO:0009796":null,"MONDO:0010557":null},"xrefs":{"Monarch":{"xref_id":"0001898"}}}


id: GO:0007090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A cell cycle process that modulates the frequency, rate or extent of the progression through the S phase of the mitotic cell cycle.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of S phase of mitotic cell cycle (obsolete GO:0007090)","synonyms":[{"name":"regulation of S phase of mitotic cell cycle","type":"exact"},{"name":"regulation of S-phase of mitotic cell cycle","type":"exact"}],"termid":"GO:0007090"}


id: PR:Q9Y7J4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An actin-related protein 2/3 complex subunit 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR12391:SF0","OMA:SCHPO03569"],"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":"actin-related protein 2/3 complex subunit 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1778.08c","secondary_identifiers":["UniProtKB:Q9Y7J4"],"synonyms":[{"name":"Spom972h-ARPC3","type":"exact"},{"name":"arp2/3 complex 21 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"p21-ARC (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9Y7J4"}


id: MONDO:0700154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm arising from skeletal muscle that occurs in dogs.","definition_xrefs":["NCIT:C129300"],"direct_ancestors":[{"relation_name":"is_a","term_name":"canine soft tissue sarcoma","termid":"MONDO:0700156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canine rhabdomyosarcoma","termid":"MONDO:0700154","xrefs":{"Monarch":{"xref_id":"0700154"}}}


id: GO:0018881
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving bromoxynil, C7H3Br2NO, a dibrominated phenol derivative with a cyano (-CN) group attached. Bromoxynil is used as a herbicide for post-emergent control of annual broadleaf weeds and works by inhibiting photosynthesis in the target plants.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"nitrile metabolic process","termid":"GO:0050898"},{"relation_name":"is_a","term_name":"organohalogen metabolic process","termid":"GO:0090345"}],"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":"bromoxynil metabolic process","secondary_identifiers":["UM-BBD_pathwayID:box"],"synonyms":[{"name":"bromoxynil metabolism","type":"exact"}],"termid":"GO:0018881"}


id: MONDO:0033199
data:
  {"annotated_genes":["SJAG_00164"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87199],"is_not":false,"summary":null,"term":"MONDO:0033199"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00164":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"hearing loss, autosomal recessive 107","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080262","MEDGEN:1622558","UMLS:C4539964","OMIM:617639","GARD:22657"],"synonyms":[{"name":"DFNB107","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 107","type":"narrow"},{"name":"deafness, autosomal recessive 107","type":"narrow"}],"termid":"MONDO:0033199","terms_by_termid":{"MONDO:0033199":null},"xrefs":{"Monarch":{"xref_id":"0033199"}}}


id: PBO:0111825
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calmodulin family","termid":"PBO:0111825"}


id: PBO:0075165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein D1 polypeptide","termid":"PBO:0075165"}


id: MONDO:0016992
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete peeling skin syndrome type B (obsolete MONDO:0016992)","termid":"MONDO:0016992","xrefs":{"Monarch":{"xref_id":"0016992"}}}


id: GO:0017164
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 nicotinic acetylcholine receptor-associated protein activity (obsolete GO:0017164)","synonyms":[{"name":"nicotinic acetylcholine receptor-associated protein activity","type":"exact"}],"termid":"GO:0017164"}


id: PR:Q9UT28
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nnt1 gene.","definition_xrefs":["UniProtKB:Q9UT28","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein N-methyltransferase nnt1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8F11.09c","synonyms":[{"name":"Spom972h-nnt1","type":"exact"},{"name":"nicotinamide N-methyltransferase-like protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT28"}


id: GO:0080028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a nitrile, an organic compound containing trivalent nitrogen attached to one carbon atom.","definition_xrefs":["PMID:18987211"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"nitrile metabolic process","termid":"GO:0050898"}],"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":"nitrile biosynthetic process","termid":"GO:0080028"}


id: MONDO:0003568
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease that involves the optic chiasma.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disorder of optic chiasm","secondary_identifiers":["ICD9:377.63","UMLS:C0155307","DOID:5655","ICD9:377.5","SCTID:70476006","MEDGEN:509905","icd11.foundation:927459952","ICD10CM:H47.4"],"synonyms":[{"name":"chiasma syndrome","type":"exact"},{"name":"chiasmal syndrome","type":"exact"},{"name":"disease of optic chiasma","type":"exact"},{"name":"disease or disorder of optic chiasma","type":"exact"},{"name":"disorder of optic chiasm","type":"exact"},{"name":"disorder of optic chiasma","type":"exact"},{"name":"optic chiasma disease","type":"exact"},{"name":"optic chiasma disease or disorder","type":"exact"}],"termid":"MONDO:0003568","xrefs":{"Monarch":{"xref_id":"0003568"}}}


id: GO:1902197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of isovaleryl-CoA(4-).","definition_xrefs":["GOC:TermGenie","PMID:11231285"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty-acyl-CoA biosynthetic process","termid":"GO:0046949"},{"relation_name":"is_a","term_name":"isovaleryl-CoA(4-) metabolic process","termid":"GO:1902195"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0006790","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"isovaleryl-CoA(4-) biosynthetic process","synonyms":[{"name":"isovaleryl-CoA(4-) anabolism","type":"exact"},{"name":"isovaleryl-CoA(4-) biosynthesis","type":"exact"},{"name":"isovaleryl-CoA(4-) formation","type":"exact"},{"name":"isovaleryl-CoA(4-) synthesis","type":"exact"}],"termid":"GO:1902197"}


id: GO:0052429
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism modulates the frequency, rate or extent of the B-cell mediated immune response of a symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of symbiont B-cell mediated immune response (obsolete GO:0052429)","synonyms":[{"name":"modulation by organism of symbiont B-cell mediated immune response","type":"exact"},{"name":"regulation by organism of symbiont B-cell mediated immune response","type":"exact"}],"termid":"GO:0052429"}


id: GO:1901189
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ephrin receptor signaling pathway.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of ephrin receptor signaling pathway","termid":"GO:1901187"},{"relation_name":"positively_regulates","term_name":"ephrin receptor signaling pathway","termid":"GO:0048013"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of ephrin receptor signaling pathway","synonyms":[{"name":"activation of Eph receptor signaling pathway","type":"exact"},{"name":"activation of Eph receptor signalling pathway","type":"exact"},{"name":"activation of ephrin receptor signaling pathway","type":"narrow"},{"name":"positive regulation of Eph receptor signaling pathway","type":"exact"},{"name":"positive regulation of Eph receptor signalling pathway","type":"exact"},{"name":"up regulation of Eph receptor signaling pathway","type":"exact"},{"name":"up regulation of Eph receptor signalling pathway","type":"exact"},{"name":"up regulation of ephrin receptor signaling pathway","type":"exact"},{"name":"up-regulation of Eph receptor signaling pathway","type":"exact"},{"name":"up-regulation of Eph receptor signalling pathway","type":"exact"},{"name":"up-regulation of ephrin receptor signaling pathway","type":"exact"},{"name":"upregulation of Eph receptor signaling pathway","type":"exact"},{"name":"upregulation of Eph receptor signalling pathway","type":"exact"},{"name":"upregulation of ephrin receptor signaling pathway","type":"exact"}],"termid":"GO:1901189"}


id: PBO:0029842
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_maintenance_of_protein_localization_to_heterochromatin_at_centromere_outer_repeat","termid":"PBO:0029842"}


id: PBO:0075805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small RNA binding exonuclease protection factor La like 4, pseudogene","termid":"PBO:0075805"}


id: GO:0061576
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that catalyzes the reaction acyl-CoA + sphingosine = CoA + N-acylsphingosine. In S. cerevisiae it contains three subunits: lag1, lac1 and lip1.","definition_xrefs":["GOC:dph","PMID:15692566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"acyl-CoA ceramide synthase complex","termid":"GO:0061576"}


id: PBO:0046862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fumarylacetoacetate hydrolase domain containing 1","termid":"PBO:0046862"}


id: PBO:0072397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 2","termid":"PBO:0072397"}


id: PBO:0048819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 5 pseudogene 3","termid":"PBO:0048819"}


id: MOD:01396
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-proline residue to a 5-hydroxy-3-methyl-L-proline.","definition_xrefs":["PubMed:8557573","RESID:AA0473","PubMed:7592021"],"direct_ancestors":[{"relation_name":"has_functional_parent","term_name":"monohydroxylated proline","termid":"MOD:01024"},{"relation_name":"has_functional_parent","term_name":"monomethylated proline","termid":"MOD:01417"},{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxy-3-methyl-L-proline (Pro)","synonyms":[{"name":"(2S,3S,5Xi)-5-hydroxy-3-methylpyrrolidine-2-carboxylic acid","type":"exact"},{"name":"5-hydroxy-3-methyl-L-proline","type":"exact"},{"name":"5-hydroxy-3-methylproline","type":"exact"},{"name":"5Hy3MePro","type":"exact"},{"name":"MOD_RES 5-hydroxy-3-methylproline (Ile)","type":"exact"},{"name":"beta-methyl-delta-hydroxyproline","type":"exact"}],"termid":"MOD:01396"}


id: GO:1903714
data:
  {"annotated_genes":["SJAG_02029","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104702,111978],"is_not":false,"summary":null,"term":"GO:1903714"}]},"cv_name":"biological_process","definition":"The directed movement of isoleucine across a membrane by means of some agent such as a transporter or a pore.","definition_xrefs":["GO_REF:0000069","PMID:18503766","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid transmembrane transport","termid":"GO:0003333"},{"relation_name":"is_a","term_name":"isoleucine transport","termid":"GO:0015818"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02029":null,"SJAG_04725":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"isoleucine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1903714","terms_by_termid":{"GO:1903714":null}}


id: PBO:0054030
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 1361","termid":"PBO:0054030"}


id: PBO:0027253
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_meiotic_centromere_clustering","termid":"PBO:0027253"}


id: GO:0019036
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Specific locations and structures in the virus infected cell involved in transcribing the viral genome.","definition_xrefs":["ISBN:0781718325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"viral transcriptional complex","termid":"GO:0019036"}


id: PBO:0088130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar membrane protein kinase; negatively regulates membrane fusion; associates with vacuolar membrane through palmitoylation of one or more cysteines in consensus sequence; vacuolar membrane association is essential to its kinase activity; mutant shows defect in CPY processing; ortholog of human serine/threonine kinase 16 (STK16)","termid":"PBO:0088130"}


id: FYPO:0004669
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to ferrozine. Cells stop growing (and may die) at a concentration of ferrozine that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0005447","FYPO:0000003","FYPO:0001985","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to ferrozine","synonyms":[{"name":"hypersensitive to ferrozine","type":"exact"},{"name":"sensitive to ferrozine during mitotic cell cycle","type":"related"},{"name":"sensitive to ferrozine during vegetative growth","type":"exact"},{"name":"sensitive to ferrozine(2-)","type":"exact"}],"termid":"FYPO:0004669"}


id: PBO:0069685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 964, pseudogene","termid":"PBO:0069685"}


id: PBO:0057435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 552","termid":"PBO:0057435"}


id: PBO:0050837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isoleucyl-tRNA synthetase 2, mitochondrial","termid":"PBO:0050837"}


id: FYPO:0007986
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed during mitotic interphase in which the localization of a protein to the microtubule overlap of cytoplasmic microtubule bundles is decreased.","definition_xrefs":["PMID:19879140","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to interphase microtubule","termid":"FYPO:0006182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein localization to interphase microtubule bundle overlap","termid":"FYPO:0007986"}


id: PBO:0109840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canto_allele_systematic_id","termid":"PBO:0109840"}


id: PBO:0047156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 184 member B","termid":"PBO:0047156"}


id: PBO:0083527
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 ORF SAS10/YDL153C, a component of the small ribosomal subunit processosome","termid":"PBO:0083527"}


id: PBO:0081848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 781","termid":"PBO:0081848"}


id: PBO:0002949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding protein Fet5 (predicted)","termid":"PBO:0002949"}


id: GO:0015878
data:
  {"annotated_genes":["SJAG_02779","SJAG_02780"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81014,73540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905135"}]},"cv_name":"biological_process","definition":"The directed movement of biotin into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Biotin is cis-tetrahydro-2-oxothieno(3,4-d)imidazoline-4-valeric acid; the (+) enantiomer is very widely distributed in cells and serves as a carrier in a number of enzymatic beta-carboxylation reactions.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transport","termid":"GO:0015718"},{"relation_name":"is_a","term_name":"amide transport","termid":"GO:0042886"},{"relation_name":"is_a","term_name":"vitamin transport","termid":"GO:0051180"},{"relation_name":"is_a","term_name":"sulfur compound transport","termid":"GO:0072348"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02779":null,"SJAG_02780":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"biotin transport","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"vitamin B7 transport","type":"exact"},{"name":"vitamin H transport","type":"exact"}],"termid":"GO:0015878","terms_by_termid":{"GO:1905135":null}}


id: GO:0042014
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-19 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:jl","GOC:signaling"],"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:0038023","GO:0003674"],"is_obsolete":false,"name":"interleukin-19 receptor activity","synonyms":[{"name":"IL-19 receptor activity","type":"exact"},{"name":"IL-19R","type":"exact"}],"termid":"GO:0042014"}


id: MONDO:0011348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital anomaly of the hand or foot, marked by the presence of supernumerary digits.","definition_xrefs":["MESH:D017689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polydactyly","termid":"MONDO:0021003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-syndromic polydactyly","secondary_identifiers":["Orphanet:2913","icd11.foundation:1534380955","MedDRA:10036063"],"synonyms":[{"name":"Extra digits","type":"related"},{"name":"isolated polydactyly","type":"related"},{"name":"isolated polydactyly (disease)","type":"exact"},{"name":"nonsyndromic polydactyly","type":"exact"},{"name":"nonsyndromic polydactyly (disease)","type":"exact"},{"name":"polydactylia","type":"related"},{"name":"supernumerary digits","type":"related"}],"termid":"MONDO:0011348","xrefs":{"Monarch":{"xref_id":"0011348"}}}


id: GO:0009789
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of abscisic acid (ABA) signaling.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of abscisic acid-activated signaling pathway","termid":"GO:0009787"},{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"positively_regulates","term_name":"abscisic acid-activated signaling pathway","termid":"GO:0009738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of abscisic acid-activated signaling pathway","synonyms":[{"name":"activation of abscisic acid mediated signaling","type":"narrow"},{"name":"positive regulation of abscisic acid mediated signaling pathway","type":"related"},{"name":"positive regulation of abscisic acid mediated signalling","type":"exact"},{"name":"stimulation of abscisic acid mediated signaling","type":"narrow"},{"name":"up regulation of abscisic acid mediated signaling","type":"exact"},{"name":"up-regulation of abscisic acid mediated signaling","type":"exact"},{"name":"upregulation of abscisic acid mediated signaling","type":"exact"}],"termid":"GO:0009789"}


id: GO:0042861
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of achromobactin, a citrate siderophore.","definition_xrefs":["GOC:jl","PMID:10928541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore biosynthetic process","termid":"GO:0019290"},{"relation_name":"is_a","term_name":"achromobactin metabolic process","termid":"GO:0042860"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"achromobactin biosynthetic process","secondary_identifiers":["GO:0031181","GO:0031182"],"synonyms":[{"name":"achromobactin anabolism","type":"exact"},{"name":"achromobactin biosynthesis","type":"exact"},{"name":"achromobactin formation","type":"exact"},{"name":"achromobactin synthesis","type":"exact"}],"termid":"GO:0042861"}


id: MONDO:0005765
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A viral infectious disease that results in infection in cattle and swine, has material basis in foot-and-mouth disease virus, which is transmitted by contaminated fomites, or transmitted by ingestion of food contaminated with infected meat or animal products. The infection results in formation of vesicles in the mouth, or on the feet and has symptom lameness.","definition_xrefs":["EFO:0007277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cattle disease","termid":"MONDO:0024913"},{"relation_name":"is_a","term_name":"swine disease","termid":"MONDO:0024990"},{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"foot and mouth disease","secondary_identifiers":["icd11.foundation:1008730501","MESH:D005536"],"termid":"MONDO:0005765","xrefs":{"Monarch":{"xref_id":"0005765"}}}


id: GO:0023044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which information is sent from one location to another, within a living organism or between living organisms, via a chemical mediator.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signaling via chemical mediator (obsolete GO:0023044)","synonyms":[{"name":"signaling via chemical mediator","type":"exact"},{"name":"signalling via chemical mediator","type":"exact"}],"termid":"GO:0023044"}


id: PBO:0055571
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 3007","termid":"PBO:0055571"}


id: PBO:0039065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AGK pseudogene 2","termid":"PBO:0039065"}


id: GO:0003793
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any activity that plays a role in the defense/immune response of an organism against infection and disease.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete defense/immunity protein activity (obsolete GO:0003793)","synonyms":[{"name":"defence/immunity protein activity","type":"exact"},{"name":"defense/immunity protein activity","type":"exact"}],"termid":"GO:0003793"}


id: PBO:0046666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epithelial splicing regulatory protein 1","termid":"PBO:0046666"}


id: PBO:0027732
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_DNA_replication_initiation","termid":"PBO:0027732"}


id: GO:0039633
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process mediated by a virus that results in the death of a cell in the host organism.","definition_xrefs":["GOC:bf","GOC:jl","GOC:bm"],"gene_count":0,"genotype_count":0,"name":"obsolete killing by virus of host cell (obsolete GO:0039633)","synonyms":[{"name":"killing by phage of host cells","type":"narrow"},{"name":"killing by virus of host cells","type":"exact"}],"termid":"GO:0039633"}


id: GO:0032868
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an insulin stimulus. Insulin is a polypeptide hormone produced by the islets of Langerhans of the pancreas in mammals, and by the homologous organs of other organisms.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to peptide hormone","termid":"GO:0043434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to insulin","synonyms":[{"name":"response to insulin stimulus","type":"exact"}],"termid":"GO:0032868"}


id: PBO:0079067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Trp (anticodon CCA) 3-1","termid":"PBO:0079067"}


id: GO:0072165
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the anterior mesonephric tubule over time, from its initial formation to the mature structure. The anterior mesonephric tubule is an epithelial tube that is part of the mesonephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesonephric tubule development","termid":"GO:0072164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"anterior mesonephric tubule development","termid":"GO:0072165"}


id: FYECO:0000333
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which all 20 standard amino acids were added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 20 standard aa's","synonyms":[{"name":"22 standard amino acids added","type":"exact"}],"termid":"FYECO:0000333"}


id: PATO:0002383
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A waxiness which is relatively low.","direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"},{"relation_name":"is_a","term_name":"waxiness","termid":"PATO:0002381"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased waxiness","termid":"PATO:0002383"}


id: PBO:0053221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich glioma inactivated 1","termid":"PBO:0053221"}


id: MONDO:0800403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited retinopathy caused by bi-allelic variants in the CNGB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"CNGB1-related retinopathy","termid":"MONDO:0800403","xrefs":{"Monarch":{"xref_id":"0800403"}}}


id: PBO:0065048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRELI domain containing 3B pseudogene 2","termid":"PBO:0065048"}


id: PBO:0117380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERPUD1 intronic transcript 1","termid":"PBO:0117380"}


id: PBO:0027054
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_curved_microtubules","termid":"PBO:0027054"}


id: PBO:0031616
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_transposition","termid":"PBO:0031616"}


id: PBO:0082814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Conserved ER protein translocation channel; essential subunit of Sec61 complex (Sec61p, Sbh1p, and Sss1p); forms channel for SRP-dependent protein import; with Sec63 complex is required for SRP-independent protein translocation into the ER; involved in posttranslational soluble protein import into the ER, ERAD of soluble substrates, and misfolded soluble protein export from the ER","termid":"PBO:0082814"}


id: PBO:0028404
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ubiquinone_binding","termid":"PBO:0028404"}


id: PBO:0026751
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_stress","termid":"PBO:0026751"}


id: MONDO:0009436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypothalamic hamartomas (HH) are rare, tumor-like malformations that occur during fetal development and are present at birth. The lesions usually do not change in size or spread to other locations. Both the type and severity of symptoms vary greatly among patients with hypothalamic hamartomas. Common symptoms include frequent gelastic seizures (spontaneous laughing, giggling and/or smirking) or dacrystic seizures (crying or grunting); developmental delays; and/or precocious puberty. Additional symptoms may include cognitive impairment; emotional and behavioral difficulties; and endocrine disturbances. These symptoms often start early in life but are frequently misdiagnosed. For some patients, endocrine (hormonal) disturbances such as central precocious puberty may be the only symptom. These patients can often be treated successfully with medications. For some, however, HH can be disabling. For those with HH and epilepsy, it is common for the disorder to progress and for different types of seizures to develop. The seizures associated with HH often cannot be well-controlled with the standard seizure medications. For some, additional treatment such as surgical removal, radiosurgery, or thermoablation may be indicated. Though hypothalamic hamartomas can occur in patients with certain genetic disorders (such as Pallister-Hall syndrome), the majority of cases are sporadic.","direct_ancestors":[{"relation_name":"is_a","term_name":"Pallister-Hall syndrome","termid":"MONDO:0007804"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital hypothalamic hamartoma syndrome","secondary_identifiers":["NCIT:C4385","UMLS:C0342418","icd11.foundation:2057991470","GARD:2934","Orphanet:2113","MESH:C537158","SCTID:237714006","ICD9:759.6","OMIM:241800","MEDGEN:137970"],"synonyms":[{"name":"Pallister-Hall-like syndrome","type":"exact"},{"name":"congenital hypothalamic hamartoma syndrome","type":"exact"},{"name":"hamartoma of hypothalamus","type":"exact"},{"name":"hamartoma of the hypothalamus","type":"related"},{"name":"hypothalamic hamartoma","type":"exact"},{"name":"hypothalamic hamartomas","type":"exact"}],"termid":"MONDO:0009436","xrefs":{"Monarch":{"xref_id":"0009436"}}}


id: PBO:0030393
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-binucleate_monoseptate_cell_(obsolete_FYPO:0001224)","termid":"PBO:0030393"}


id: PBO:0108979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPMIP3 pseudogene 1","termid":"PBO:0108979"}


id: PR:G2TRL6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1B2.06 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRL6"],"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 C1B2.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B2.06","synonyms":[{"name":"Spom972h-SPAC1B2.06","type":"exact"}],"termid":"PR:G2TRL6"}


id: PBO:0050188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosome binding domain 1 pseudogene 5","termid":"PBO:0050188"}


id: GO:0044232
data:
  {"annotated_genes":["SJAG_02501","SJAG_01329","SJAG_03170","SJAG_02578","SJAG_02002","SJAG_03247","SJAG_04552","SJAG_05184","SJAG_02028","SJAG_05241","SJAG_03710","SJAG_01168","SJAG_01305","SJAG_01929","SJAG_03282","SJAG_03416","SJAG_01116","SJAG_02613","SJAG_04413","SJAG_01564","SJAG_04370","SJAG_04221"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[78762,119520,120687,113623,93314,99327,106279],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140268"},{"annotations":[117181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098853"},{"annotations":[71679,81866,118598,76529,71722],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032865"},{"annotations":[108251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044233"},{"annotations":[109250,111971,103598,76818,91317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044284"},{"annotations":[117182,108253,79055,108953],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071561"},{"annotations":[92041,96160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990816"}]},"cv_name":"cellular_component","definition":"A zone of apposition between the membranes of an organelle with another membrane, either another membrane of the same organelle, a membrane of another organelle, or the plasma membrane. Membrane contact sites (MCSs) are structured by bridging complexes. They are specialized for communication, including the efficient traffic of small molecules such as Ca2+ ions and lipids, as well as enzyme-substrate interactions.","definition_xrefs":["GOC:jl","PMID:16806880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"organelle","termid":"GO:0043226"}],"gene_count":22,"genes_by_uniquename":{"SJAG_01116":null,"SJAG_01168":null,"SJAG_01305":null,"SJAG_01329":null,"SJAG_01564":null,"SJAG_01929":null,"SJAG_02002":null,"SJAG_02028":null,"SJAG_02501":null,"SJAG_02578":null,"SJAG_02613":null,"SJAG_03170":null,"SJAG_03247":null,"SJAG_03282":null,"SJAG_03416":null,"SJAG_03710":null,"SJAG_04221":null,"SJAG_04370":null,"SJAG_04413":null,"SJAG_04552":null,"SJAG_05184":null,"SJAG_05241":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"organelle membrane contact site","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"MCS","type":"exact"},{"name":"inter-organelle junction","type":"narrow"},{"name":"interorganelle junction","type":"narrow"}],"termid":"GO:0044232","terms_by_termid":{"GO:0032865":null,"GO:0044233":null,"GO:0044284":null,"GO:0071561":null,"GO:0098853":null,"GO:0140268":null,"GO:1990816":null}}


id: PBO:0062514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily J member 3","termid":"PBO:0062514"}


id: MONDO:0009980
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":"retinal telangiectasia and hypogammaglobulinemia","secondary_identifiers":["UMLS:C2930961","MEDGEN:419680","OMIM:267900","MESH:C535638"],"synonyms":[{"name":"Frenkel Russe syndrome","type":"related"},{"name":"retinal telangiectasia and hypogammaglobulinemia","type":"exact"},{"name":"retinal telangiectasia associated with hypogammaglobulinemia","type":"related"}],"termid":"MONDO:0009980","xrefs":{"Monarch":{"xref_id":"0009980"}}}


id: MONDO:0001717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"corneal deposit","termid":"MONDO:0001308"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"posterior corneal pigmentation","secondary_identifiers":["MEDGEN:509792","ICD9:371.13","SCTID:267639001","UMLS:C0155106","DOID:13448"],"synonyms":[{"name":"posterior corneal pigmentations","type":"exact"}],"termid":"MONDO:0001717","xrefs":{"Monarch":{"xref_id":"0001717"}}}


id: MONDO:0018174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary glaucoma is a clinically diverse group of rare eye disorders with genetic predisposition characterized by elevated intraocular pressure (IOP) and glaucomatous changes of the optic nerve head, leading to field defects, visual loss and blindness. Hereditary glaucoma can be sub-classified as primary (congenital glaucoma, juvenile glaucoma) or secondary according to the presence or absence of systemic or other ocular anomalies (iridogoniodysgenesis, Stickler syndrome, Coats syndrome). The clinical presentation is variable and is based on age, severity of glaucoma, presence of ocular abnormalities and development of secondary IOP related abnormalities.","definition_xrefs":["Orphanet:359"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic developmental defect of the eye (obsolete MONDO:0015217)","termid":"MONDO:0015217"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"glaucoma","termid":"MONDO:0005041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"hereditary glaucoma","secondary_identifiers":["MEDGEN:777991","MESH:C580055","UMLS:C3711383","GARD:2486"],"synonyms":[{"name":"glaucoma, hereditary","type":"related"},{"name":"hereditary glaucoma (disease)","type":"exact"}],"termid":"MONDO:0018174","xrefs":{"Monarch":{"xref_id":"0018174"}}}


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


id: MONDO:0021251
data:
  {"annotated_genes":["SJAG_02748","SJAG_01419"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89075,86861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011962"}]},"cv_name":"mondo","definition":"A neoplasm (disease) that involves the endometrium.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrial disorder","termid":"MONDO:0000931"},{"relation_name":"is_a","term_name":"tumor of uterus","termid":"MONDO:0021353"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01419":null,"SJAG_02748":null},"genotype_count":0,"is_obsolete":false,"name":"endometrium neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:239.5","MEDGEN:8619","UMLS:C0014170","NCIT:C3012","MESH:D016889","SCTID:123844007"],"synonyms":[{"name":"endometrial neoplasm","type":"exact"},{"name":"endometrial tumor","type":"exact"},{"name":"endometrial tumour","type":"exact"},{"name":"endometrium neoplasm (disease)","type":"exact"},{"name":"endometrium tumor","type":"exact"},{"name":"endometrium tumour","type":"exact"},{"name":"neoplasm of endometrium","type":"exact"},{"name":"neoplasm of the endometrium","type":"exact"},{"name":"tumor of endometrium","type":"exact"},{"name":"tumor of the endometrium","type":"exact"},{"name":"tumour of endometrium","type":"exact"},{"name":"tumour of the endometrium","type":"exact"}],"termid":"MONDO:0021251","terms_by_termid":{"MONDO:0011962":null},"xrefs":{"Monarch":{"xref_id":"0021251"}}}


id: FYPO:0002166
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which polynucleotide 3'-phosphatase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal polynucleotide 3'-phosphatase activity","termid":"FYPO:0002165"},{"relation_name":"is_a","term_name":"abolished phosphatase activity","termid":"FYPO:0004303"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000661","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"abolished polynucleotide 3'-phosphatase activity","synonyms":[{"name":"polynucleotide 3'-phosphatase activity abolished","type":"exact"}],"termid":"FYPO:0002166"}


id: PBO:0066964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 266","termid":"PBO:0066964"}


id: GO:0040021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The determination of sex and sexual phenotype in the germ line of a hermaphrodite.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"germ-line sex determination","termid":"GO:0018992"}],"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":"hermaphrodite germ-line sex determination","secondary_identifiers":["GO:0042005"],"termid":"GO:0040021"}


id: PBO:0052492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 6","termid":"PBO:0052492"}


id: GO:0050679
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the rate or extent of epithelial cell proliferation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell population proliferation","termid":"GO:0008284"},{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation","termid":"GO:0050678"},{"relation_name":"positively_regulates","term_name":"epithelial cell proliferation","termid":"GO:0050673"}],"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 epithelial cell proliferation","synonyms":[{"name":"activation of epithelial cell proliferation","type":"narrow"},{"name":"stimulation of epithelial cell proliferation","type":"narrow"},{"name":"up regulation of epithelial cell proliferation","type":"exact"},{"name":"up-regulation of epithelial cell proliferation","type":"exact"},{"name":"upregulation of epithelial cell proliferation","type":"exact"}],"termid":"GO:0050679"}


id: MONDO:0005536
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ulcerative colitis that involves the entire colon.","direct_ancestors":[{"relation_name":"is_a","term_name":"ulcerative colitis","termid":"MONDO:0005101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"pancolitis","secondary_identifiers":["EFO:0005626","MEDGEN:1720692","NANDO:1200450","UMLS:C0868908"],"synonyms":[{"name":"pan-ulcerative colitis","type":"exact"},{"name":"universal colitis","type":"exact"}],"termid":"MONDO:0005536","xrefs":{"Monarch":{"xref_id":"0005536"}}}


id: GO:0030977
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to taurine.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkanesulfonate binding","termid":"GO:0043210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"taurine binding","termid":"GO:0030977"}


id: GO:0065004
data:
  {"annotated_genes":["SJAG_03220","SJAG_02458","SJAG_00757","SJAG_04581","SJAG_00873","SJAG_01823","SJAG_02079","SJAG_01708","SJAG_02314","SJAG_02198","SJAG_00303","SJAG_01837","SJAG_02813","SJAG_04274","SJAG_01808","SJAG_02908","SJAG_03900","SJAG_04530","SJAG_03619","SJAG_04177","SJAG_00336","SJAG_03867","SJAG_00684","SJAG_00718","SJAG_01475","SJAG_03217","SJAG_04995","SJAG_02667","SJAG_03905","SJAG_02303","SJAG_03956","SJAG_03095","SJAG_00939","SJAG_03183","SJAG_04257","SJAG_03048","SJAG_03685","SJAG_02872","SJAG_00327","SJAG_00170","SJAG_05273","SJAG_03120","SJAG_03221","SJAG_00756","SJAG_02607","SJAG_01207","SJAG_04272","SJAG_00247","SJAG_01410","SJAG_02119","SJAG_03542","SJAG_02691","SJAG_00045","SJAG_02465","SJAG_00942","SJAG_04654","SJAG_00307","SJAG_00741","SJAG_04696","SJAG_04547","SJAG_02664","SJAG_02513","SJAG_03007","SJAG_02906","SJAG_04038","SJAG_01771","SJAG_02267","SJAG_03285","SJAG_04638","SJAG_01378","SJAG_02708","SJAG_01611","SJAG_00766","SJAG_04879","SJAG_02074","SJAG_00692","SJAG_02174","SJAG_01523","SJAG_05321","SJAG_04989"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90690,94633,101267,108291,109277,91885,101015,120863,115083,73096,81623,117062,104808,97333,116200,118451,96552,119687,120827,103962],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034080"},{"annotations":[117385,109279,111892,115537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140529"},{"annotations":[74063,66093,66934,76867,77548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000730"},{"annotations":[65588,57270,67531,81690,92606,107395,67987],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051382"},{"annotations":[105221],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140530"},{"annotations":[80335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000707"},{"annotations":[109595,112255],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010772"},{"annotations":[57340,73739,80048],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902977"},{"annotations":[112517,117005,105223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902985"},{"annotations":[119942],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905560"},{"annotations":[116521,109664,92948,71607,62938,92946,80654,74769,75022,98321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006334"},{"annotations":[110927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006294"},{"annotations":[91474,118660,104273],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905561"},{"annotations":[91533,81360],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045899"},{"annotations":[79267,64999,69862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001188"},{"annotations":[95989,72228,72377,77342,73799,76720,75405,76201,73110,78613,79045,68718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051123"},{"annotations":[73557,104971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070898"},{"annotations":[101606,110058,117930],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905324"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of proteins and DNA molecules to form a protein-DNA complex.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"is_a","term_name":"protein-DNA complex organization","termid":"GO:0071824"}],"gene_count":80,"genes_by_uniquename":{"SJAG_00045":null,"SJAG_00170":null,"SJAG_00247":null,"SJAG_00303":null,"SJAG_00307":null,"SJAG_00327":null,"SJAG_00336":null,"SJAG_00684":null,"SJAG_00692":null,"SJAG_00718":null,"SJAG_00741":null,"SJAG_00756":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00873":null,"SJAG_00939":null,"SJAG_00942":null,"SJAG_01207":null,"SJAG_01378":null,"SJAG_01410":null,"SJAG_01475":null,"SJAG_01523":null,"SJAG_01611":null,"SJAG_01708":null,"SJAG_01771":null,"SJAG_01808":null,"SJAG_01823":null,"SJAG_01837":null,"SJAG_02074":null,"SJAG_02079":null,"SJAG_02119":null,"SJAG_02174":null,"SJAG_02198":null,"SJAG_02267":null,"SJAG_02303":null,"SJAG_02314":null,"SJAG_02458":null,"SJAG_02465":null,"SJAG_02513":null,"SJAG_02607":null,"SJAG_02664":null,"SJAG_02667":null,"SJAG_02691":null,"SJAG_02708":null,"SJAG_02813":null,"SJAG_02872":null,"SJAG_02906":null,"SJAG_02908":null,"SJAG_03007":null,"SJAG_03048":null,"SJAG_03095":null,"SJAG_03120":null,"SJAG_03183":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03221":null,"SJAG_03285":null,"SJAG_03542":null,"SJAG_03619":null,"SJAG_03685":null,"SJAG_03867":null,"SJAG_03900":null,"SJAG_03905":null,"SJAG_03956":null,"SJAG_04038":null,"SJAG_04177":null,"SJAG_04257":null,"SJAG_04272":null,"SJAG_04274":null,"SJAG_04530":null,"SJAG_04547":null,"SJAG_04581":null,"SJAG_04638":null,"SJAG_04654":null,"SJAG_04696":null,"SJAG_04879":null,"SJAG_04989":null,"SJAG_04995":null,"SJAG_05273":null,"SJAG_05321":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"protein-DNA complex assembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"DNA-protein complex assembly","type":"exact"}],"termid":"GO:0065004","terms_by_termid":{"GO:0000707":null,"GO:0000730":null,"GO:0001188":null,"GO:0006294":null,"GO:0006334":null,"GO:0010772":null,"GO:0034080":null,"GO:0045899":null,"GO:0051123":null,"GO:0051382":null,"GO:0070898":null,"GO:0140529":null,"GO:0140530":null,"GO:1902977":null,"GO:1902985":null,"GO:1905324":null,"GO:1905560":null,"GO:1905561":null}}


id: GO:0016483
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Increases the activity of the enzyme tryptophase hydroxylase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme activator activity","termid":"GO:0008047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0140677"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0140677","GO:0098772"],"is_obsolete":false,"name":"tryptophan hydroxylase activator activity","termid":"GO:0016483"}


id: PBO:0047042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 106 member C","termid":"PBO:0047042"}


id: PR:O13929
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A programmed cell death protein 5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR10840:SF0","OMA:SCHPO00414"],"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 C23C4.09c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23C4.09c","secondary_identifiers":["UniProtKB:O13929"],"synonyms":[{"name":"Spom972h-PDCD5","type":"exact"}],"termid":"PR:O13929"}


id: GO:0006033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which chitin is transported to, or maintained in, a specific location.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide localization","termid":"GO:0033037"}],"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":"chitin localization","synonyms":[{"name":"chitin localisation","type":"exact"},{"name":"establishment and maintenance of chitin localization","type":"exact"}],"termid":"GO:0006033"}


id: GO:0010648
data:
  {"annotated_genes":["SJAG_04522","SJAG_00975","SJAG_03678","SJAG_04551","SJAG_03072","SJAG_02336","SJAG_02169","SJAG_03508","SJAG_00289","SJAG_00824","SJAG_02765","SJAG_03126","SJAG_00990","SJAG_03501","SJAG_00424","SJAG_00883","SJAG_00610","SJAG_01245","SJAG_04943","SJAG_02000","SJAG_02233","SJAG_06270","SJAG_02311","SJAG_00169","SJAG_01983","SJAG_02392","SJAG_01297","SJAG_00229","SJAG_03681","SJAG_00526","SJAG_03893","SJAG_02389","SJAG_01142","SJAG_00991","SJAG_00875","SJAG_04206","SJAG_03799","SJAG_00209","SJAG_04825","SJAG_02858","SJAG_01464","SJAG_00266","SJAG_01386","SJAG_00457","SJAG_03486","SJAG_03353","SJAG_05346","SJAG_04455","SJAG_02481","SJAG_04462","SJAG_00642","SJAG_01114","SJAG_02451","SJAG_02231","SJAG_03592","SJAG_02379","SJAG_02514","SJAG_03974","SJAG_01253","SJAG_01184","SJAG_04259","SJAG_03263","SJAG_01790","SJAG_00293","SJAG_03185","SJAG_03355","SJAG_02426","SJAG_01679","SJAG_04910","SJAG_02013","SJAG_03089","SJAG_05000","SJAG_04249"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109161,115755,101468,105796,110193,113924,92549,117883,116248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[94592,109906,102327,93926,118364],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110034"},{"annotations":[102886,118111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106057"},{"annotations":[97712,101317,108973,109543,105704,120326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903138"},{"annotations":[91259,104039,104744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902660"},{"annotations":[90019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043409"},{"annotations":[96044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[97834,119070,101319,120327,93502,96894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903753"},{"annotations":[109067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180040"},{"annotations":[95164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090029"},{"annotations":[74079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046580"},{"annotations":[73284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035024"},{"annotations":[109473,101470,94685,112121,117886,93571,92553,103166,94770,106960,74661,97499,109162,95299,109028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031030"},{"annotations":[107819,93072,113674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000639"},{"annotations":[74924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032007"},{"annotations":[75410,62842,104913,97962,100752,103350,111217,101452,95170,115128,81718,89832,120037,109079,120230,116556,118112,115952,111625,119033,118468,107052,75303],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904262"},{"annotations":[118257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903940"}]},"cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of cell communication. Cell communication is the process that mediates interactions between a cell and its surroundings. Encompasses interactions such as signaling or attachment between one cell and another cell, between a cell and an extracellular matrix, or between a cell and any other aspect of its environment.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication","termid":"GO:0010646"},{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"negatively_regulates","term_name":"cell communication","termid":"GO:0007154"}],"gene_count":73,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00209":null,"SJAG_00229":null,"SJAG_00266":null,"SJAG_00289":null,"SJAG_00293":null,"SJAG_00424":null,"SJAG_00457":null,"SJAG_00526":null,"SJAG_00610":null,"SJAG_00642":null,"SJAG_00824":null,"SJAG_00875":null,"SJAG_00883":null,"SJAG_00975":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_01114":null,"SJAG_01142":null,"SJAG_01184":null,"SJAG_01245":null,"SJAG_01253":null,"SJAG_01297":null,"SJAG_01386":null,"SJAG_01464":null,"SJAG_01679":null,"SJAG_01790":null,"SJAG_01983":null,"SJAG_02000":null,"SJAG_02013":null,"SJAG_02169":null,"SJAG_02231":null,"SJAG_02233":null,"SJAG_02311":null,"SJAG_02336":null,"SJAG_02379":null,"SJAG_02389":null,"SJAG_02392":null,"SJAG_02426":null,"SJAG_02451":null,"SJAG_02481":null,"SJAG_02514":null,"SJAG_02765":null,"SJAG_02858":null,"SJAG_03072":null,"SJAG_03089":null,"SJAG_03126":null,"SJAG_03185":null,"SJAG_03263":null,"SJAG_03353":null,"SJAG_03355":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03508":null,"SJAG_03592":null,"SJAG_03678":null,"SJAG_03681":null,"SJAG_03799":null,"SJAG_03893":null,"SJAG_03974":null,"SJAG_04206":null,"SJAG_04249":null,"SJAG_04259":null,"SJAG_04455":null,"SJAG_04462":null,"SJAG_04522":null,"SJAG_04551":null,"SJAG_04825":null,"SJAG_04910":null,"SJAG_04943":null,"SJAG_05000":null,"SJAG_05346":null,"SJAG_06270":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 cell communication","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0010648","terms_by_termid":{"GO:0031030":null,"GO:0032007":null,"GO:0035024":null,"GO:0043409":null,"GO:0046580":null,"GO:0090029":null,"GO:0106057":null,"GO:0110034":null,"GO:0140499":null,"GO:0180040":null,"GO:1902426":null,"GO:1902660":null,"GO:1903138":null,"GO:1903753":null,"GO:1903940":null,"GO:1904262":null,"GO:2000639":null}}


id: PBO:0049798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperpolarization activated cyclic nucleotide gated potassium channel 4","termid":"PBO:0049798"}


id: PBO:0087202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-adenosyl-L-methionine-dependent tRNA: m5C-methyltransferase; methylates cytosine to m5C at several positions in tRNAs and intron-containing pre-tRNAs; increases proportion of tRNALeu(CAA) with m5C at wobble position in response to hydrogen peroxide, causing selective translation of mRNA from genes enriched in TTG codon; loss of NCL1 confers hypersensitivity to oxidative stress; similar to Nop2p and human proliferation associated nucleolar protein p120","termid":"PBO:0087202"}


id: SO:1001280
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The recoding stimulatory signal located upstream of the recoding site.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"recoding_stimulatory_region","termid":"SO:1001268"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_prime_recoding_site","synonyms":[{"name":"five prime recoding site","type":"exact"}],"termid":"SO:1001280"}


id: MONDO:0006488
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive mixed epithelial and mesenchymal neoplasm that arises from the vagina and is characterized by the presence of a malignant epithelial component and a malignant mesenchymal component.","definition_xrefs":["NCIT:C40278"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"vaginal carcinoma","termid":"MONDO:0015867"},{"relation_name":"is_a","term_name":"malignant vaginal mixed epithelial and mesenchymal neoplasm","termid":"MONDO:0037746"}],"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":"vaginal carcinosarcoma","secondary_identifiers":["DOID:136","UMLS:C1519918","MEDGEN:275573"],"synonyms":[{"name":"malignant vaginal mixed epithelial and mesenchymal tumor","type":"related"},{"name":"malignant vaginal mixed epithelial and mesenchymal tumour","type":"related"},{"name":"vaginal carcinosarcoma","type":"exact"},{"name":"vaginal malignant mixed Mullerian tumor","type":"related"},{"name":"vaginal malignant mixed Mullerian tumour","type":"related"},{"name":"vaginal malignant mixed mesodermal (Mullerian) tumor","type":"related"},{"name":"vaginal malignant mixed mesodermal (Mullerian) tumour","type":"related"},{"name":"vaginal malignant mixed mesodermal (Müllerian) tumor","type":"exact"},{"name":"vaginal malignant mixed mesodermal (Müllerian) tumour","type":"exact"},{"name":"vaginal mixed epithelial and mesenchymal tumor","type":"related"},{"name":"vaginal mixed epithelial and mesenchymal tumour","type":"related"}],"termid":"MONDO:0006488","xrefs":{"Monarch":{"xref_id":"0006488"}}}


id: PBO:0029780
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_curved_elongated_vegetative_cell_with_abnormal_septum","termid":"PBO:0029780"}


id: PBO:0012292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FACT complex subunit Pob3","termid":"PBO:0012292"}


id: MONDO:0014907
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Jeune syndrome","termid":"MONDO:0018770"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"short-rib thoracic dysplasia 15 with polydactyly","secondary_identifiers":["UMLS:C4310724","GARD:16185","OMIM:617088","MEDGEN:934691"],"synonyms":[{"name":"SRTD15","type":"exact"},{"name":"short-rib thoracic dysplasia 15 with polydactyly","type":"exact"},{"name":"short-rib thoracic dysplasia 15 with polydactyly; SRTD15","type":"exact"}],"termid":"MONDO:0014907","xrefs":{"Monarch":{"xref_id":"0014907"}}}


id: PBO:0004001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-like protein modifier Ned8","termid":"PBO:0004001"}


id: PBO:0113753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein, predicted plasma membrane receptor (Pfam-N)","termid":"PBO:0113753"}


id: GO:0044217
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any constituent part of a secondary organism with which the first organism is interacting.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"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":"other organism part","termid":"GO:0044217"}


id: PBO:0068980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 224, pseudogene","termid":"PBO:0068980"}


id: MONDO:0003952
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A choriocarcinoma of the central nervous system that occurs in an adult.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult central nervous system germ cell tumor","termid":"MONDO:0003405"},{"relation_name":"is_a","term_name":"choriocarcinoma of the central nervous system","termid":"MONDO:0016740"}],"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 central nervous system choriocarcinoma","secondary_identifiers":["UMLS:C1370505","DOID:6634","MEDGEN:234582","NCIT:C5793"],"synonyms":[{"name":"adult CNS choriocarcinoma","type":"exact"},{"name":"adult central nervous system choriocarcinoma","type":"exact"},{"name":"adult choriocarcinoma of the central nervous system","type":"exact"},{"name":"central nervous system choriocarcinoma","type":"broad"},{"name":"choriocarcinoma of adult CNS","type":"exact"},{"name":"choriocarcinoma of adult central nervous system","type":"exact"},{"name":"choriocarcinoma of the adult CNS","type":"exact"},{"name":"choriocarcinoma of the adult central nervous system","type":"exact"},{"name":"choriocarcinoma of the central nervous system of adults","type":"exact"}],"termid":"MONDO:0003952","xrefs":{"Monarch":{"xref_id":"0003952"}}}


id: MONDO:0958185
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial trifunctional protein deficiency","termid":"MONDO:0012172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005336","MONDO:0004069","MONDO:0002525"],"is_obsolete":false,"name":"mitochondrial trifunctional protein deficiency 2","secondary_identifiers":["OMIM:620300","UMLS:C5830374","MEDGEN:1841010"],"termid":"MONDO:0958185","xrefs":{"Monarch":{"xref_id":"0958185"}}}


id: GO:0009761
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The combination of atmospheric CO2 with a 3-carbon molecule phosphoenol pyruvate (PEP) to make malic acid. The malic acid is then passed into the vacuole where it is stored until daylight, when it is shuttled back out to be used as a substrate in the light reaction of photosynthesis.","definition_xrefs":["ISBN:0582015952"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon fixation","termid":"GO:0015977"},{"relation_name":"is_a","term_name":"photosynthesis, dark reaction","termid":"GO:0019685"}],"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:0008150","GO:0005975"],"is_obsolete":false,"name":"CAM photosynthesis","secondary_identifiers":["Wikipedia:Crassulacean_acid_metabolism"],"termid":"GO:0009761"}


id: PBO:0058348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4721","termid":"PBO:0058348"}


id: PBO:0054844
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 2258","termid":"PBO:0054844"}


id: GO:0090125
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of the pre-synaptic cell to the post-synaptic cell via adhesion molecules that contributes to synapse maturation.","definition_xrefs":["GOC:ascb_2009","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion","termid":"GO:0098609"},{"relation_name":"part_of","term_name":"synapse maturation","termid":"GO:0060074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"cell-cell adhesion involved in synapse maturation","synonyms":[{"name":"trans-synaptic adhesion","type":"exact"}],"termid":"GO:0090125"}


id: GO:1990583
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases the activity of the enzyme phospholipase D.","definition_xrefs":["PMID:7972129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase activator activity","termid":"GO:0016004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0030234","GO:0098772","GO:0140677"],"is_obsolete":false,"name":"phospholipase D activator activity","termid":"GO:1990583"}


id: GO:0045144
data:
  {"annotated_genes":["SJAG_00207","SJAG_04508","SJAG_00678","SJAG_03989","SJAG_00646"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89814,113646,115198],"is_not":false,"summary":null,"term":"GO:0045144"},{"annotations":[89677,95674],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051456"}]},"cv_name":"biological_process","definition":"The cell cycle process in which sister chromatids are organized and then physically separated and randomly apportioned to two sets during the second division of the meiotic cell cycle.","definition_xrefs":["GOC:ai","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sister chromatid segregation","termid":"GO:0000819"},{"relation_name":"is_a","term_name":"meiotic chromosome segregation","termid":"GO:0045132"},{"relation_name":"is_a","term_name":"chromosome organization involved in meiotic cell cycle","termid":"GO:0070192"},{"relation_name":"part_of","term_name":"meiosis II","termid":"GO:0007135"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00207":null,"SJAG_00646":null,"SJAG_00678":null,"SJAG_03989":null,"SJAG_04508":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0140013","GO:0007049"],"is_obsolete":false,"name":"meiotic sister chromatid segregation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"meiosis II, chromosome segregation","type":"exact"}],"termid":"GO:0045144","terms_by_termid":{"GO:0045144":null,"GO:0051456":null}}


id: PBO:0070465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5","termid":"PBO:0070465"}


