# terms

id: GO:0043264
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Organized structure of distinctive morphology and function, not bounded by a lipid bilayer membrane and occurring outside the cell.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membraneless organelle","termid":"GO:0043228"},{"relation_name":"is_a","term_name":"extracellular organelle","termid":"GO:0043230"}],"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 membraneless organelle","synonyms":[{"name":"extracellular non-membrane-bounded organelle","type":"exact"},{"name":"extracellular non-membrane-enclosed organelle","type":"exact"}],"termid":"GO:0043264"}


id: MONDO:0858999
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KDM3B-related intellectual disability-facial dysmorphism-short stature syndrome","secondary_identifiers":["Orphanet:633004"],"termid":"MONDO:0858999","xrefs":{"Monarch":{"xref_id":"0858999"}}}


id: PBO:0025551
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"combined malonic and methylmalonic aciduria","termid":"PBO:0025551"}


id: GO:0045989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of striated muscle contraction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of striated muscle contraction","termid":"GO:0006942"},{"relation_name":"is_a","term_name":"positive regulation of muscle contraction","termid":"GO:0045933"},{"relation_name":"positively_regulates","term_name":"striated muscle contraction","termid":"GO:0006941"}],"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 striated muscle contraction","synonyms":[{"name":"activation of striated muscle contraction","type":"narrow"},{"name":"stimulation of striated muscle contraction","type":"narrow"},{"name":"up regulation of striated muscle contraction","type":"exact"},{"name":"up-regulation of striated muscle contraction","type":"exact"},{"name":"upregulation of striated muscle contraction","type":"exact"}],"termid":"GO:0045989"}


id: GO:0002903
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of B cell apoptotic process.","definition_xrefs":["GOC:add","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of B cell apoptotic process","termid":"GO:0002902"},{"relation_name":"is_a","term_name":"negative regulation of lymphocyte apoptotic process","termid":"GO:0070229"},{"relation_name":"negatively_regulates","term_name":"B cell apoptotic process","termid":"GO:0001783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of B cell apoptotic process","synonyms":[{"name":"down regulation of B cell apoptosis","type":"exact"},{"name":"down-regulation of B cell apoptosis","type":"exact"},{"name":"downregulation of B cell apoptosis","type":"exact"},{"name":"inhibition of B cell apoptosis","type":"narrow"},{"name":"negative regulation of B cell apoptosis","type":"narrow"}],"termid":"GO:0002903"}


id: PBO:0030458
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_nickel_import","termid":"PBO:0030458"}


id: PBO:0041539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 17 open reading frame 80","termid":"PBO:0041539"}


id: GO:0002383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An immune response taking place in the brain or nervous system.","definition_xrefs":["GO_REF:0000022","GOC:jal","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organ or tissue specific immune response","termid":"GO:0002251"}],"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":"immune response in brain or nervous system","termid":"GO:0002383"}


id: MONDO:0016704
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete glial tumor of neuroepithelial tissue with unknown origin (obsolete MONDO:0016704)","secondary_identifiers":["Orphanet:251668"],"termid":"MONDO:0016704","xrefs":{"Monarch":{"xref_id":"0016704"}}}


id: PBO:0043556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type IV alpha 5 chain","termid":"PBO:0043556"}


id: GO:0050503
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: trehalose 6-phosphate + phosphate = glucose 6-phosphate + beta-D-glucose 1-phosphate.","definition_xrefs":["EC:2.4.1.216","MetaCyc:2.4.1.216-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"1,4-alpha-oligoglucan phosphorylase activity","termid":"GO:0004645"}],"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:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016757","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"trehalose 6-phosphate phosphorylase activity","secondary_identifiers":["RHEA:20864"],"synonyms":[{"name":"trehalose 6-phosphate:phosphate beta-D-glucosyltransferase activity","type":"related"}],"termid":"GO:0050503"}


id: PBO:0072828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAMSN1 antisense RNA 1","termid":"PBO:0072828"}


id: MONDO:0004785
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the eyelids near the eyelashes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eyelid disorder","termid":"MONDO:0003382"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"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":"blepharitis","secondary_identifiers":["EFO:0009536","UMLS:C0005741","ICD9:373.8","NCIT:C112183","ICD10CM:H01.0","ICD9:373.0","DOID:9423","MEDGEN:598","ICD9:373.9","ICD9:373.4","SCTID:41446000","ICD9:373.00","MESH:D001762"],"synonyms":[{"name":"eyelid inflammation","type":"exact"},{"name":"inflammation of eyelid","type":"exact"}],"termid":"MONDO:0004785","xrefs":{"Monarch":{"xref_id":"0004785"}}}


id: MONDO:0015309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Auriculocondylar syndrome (obsolete MONDO:0015309)","termid":"MONDO:0015309","xrefs":{"Monarch":{"xref_id":"0015309"}}}


id: PBO:0116321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F1-FO ATP synthase epsilon subunit (central stalk) Atp15","termid":"PBO:0116321"}


id: MONDO:0100163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A inflammatory syndrome in children infected by the SARS-CoV-2 with similarities to Kawasaki disease. Clinical manifestations range from fever and inflammation to myocardial injury, shock, and development of coronary artery aneurysms.","definition_xrefs":["PMID:32511692","PMID:32529358","PMID:32630212"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease","termid":"MONDO:0005108"},{"relation_name":"is_a","term_name":"multisystem inflammatory syndrome in children and adults","termid":"MONDO:0035375"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COVID-19–associated multisystem inflammatory syndrome in children","secondary_identifiers":["DOID:0080711","NCIT:C172127"],"synonyms":[{"name":"COVID-19 -related paediatric inflammatory multisystem syndrome","type":"exact"},{"name":"COVID-19 -related pediatric inflammatory multisystem syndrome","type":"exact"},{"name":"COVID-19 Kawasaki-like syndrome","type":"exact"},{"name":"COVID-19 associated multisystem inflammatory syndrome in children","type":"exact"},{"name":"MIS-C","type":"exact"},{"name":"PIMS","type":"exact"},{"name":"PIMS-TS","type":"exact"},{"name":"PMIS","type":"exact"},{"name":"SARS-CoV-2 Kawasaki-like syndrome","type":"exact"},{"name":"multisystem inflammatory syndrome in children","type":"exact"},{"name":"multisystem inflammatory syndrome in children associated with COVID-19","type":"exact"},{"name":"multisystem inflammatory syndrome in children associated with coronavirus disease 2019","type":"exact"},{"name":"paediatric inflammatory multisystem syndrome","type":"exact"},{"name":"paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2","type":"exact"},{"name":"paediatric inflammatory multisystem syndrome: temporally associated with SARS-CoV-2","type":"exact"},{"name":"paediatric multi-system inflammatory syndrome potentially associated with COVID-19","type":"exact"},{"name":"paediatric multisystem inflammatory syndrome","type":"exact"},{"name":"pediatric inflammatory multisystem syndrome","type":"exact"},{"name":"pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2","type":"exact"},{"name":"pediatric inflammatory multisystem syndrome: temporally associated with SARS-CoV-2","type":"exact"},{"name":"pediatric multi-system inflammatory syndrome potentially associated with COVID-19","type":"exact"},{"name":"pediatric multisystem inflammatory syndrome","type":"exact"}],"termid":"MONDO:0100163","xrefs":{"Monarch":{"xref_id":"0100163"}}}


id: FYPO:0000518
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 nuclear transport is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear transport","termid":"FYPO:0005573"},{"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal nuclear transport during vegetative growth","synonyms":[{"name":"abnormal nuclear transport during mitotic cell cycle","type":"related"},{"name":"nuclear transport: abnormal during vegetative growth","type":"related"}],"termid":"FYPO:0000518"}


id: PBO:0057766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 2110","termid":"PBO:0057766"}


id: MONDO:0022633
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"camptodactyly joint contractures and facial skeletal dysplasia","secondary_identifiers":["MEDGEN:419868","UMLS:C2931678","MESH:C537969"],"termid":"MONDO:0022633","xrefs":{"Monarch":{"xref_id":"0022633"}}}


id: GO:0051316
data:
  {"annotated_genes":["SJAG_01211","SJAG_01837","SJAG_03989","SJAG_05266","SJAG_00418","SJAG_03217","SJAG_01775","SJAG_02346","SJAG_03683","SJAG_03327","SJAG_00918","SJAG_03220","SJAG_04508","SJAG_00678","SJAG_01371","SJAG_04076","SJAG_03926","SJAG_05319","SJAG_02814","SJAG_05220","SJAG_01278","SJAG_03437","SJAG_01224","SJAG_01805","SJAG_00794","SJAG_02731"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116110],"is_not":false,"summary":null,"term":"GO:0051316"},{"annotations":[93331,87383],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051456"},{"annotations":[116125],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1904967"},{"annotations":[101928,93312,109772,97405,89260,95063,94814,90494,107290,109354,109813,100827,112673,116361,106971,108604,115370,100013,108344,104947,113541,88656,98134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051455"}]},"cv_name":"biological_process","definition":"The cellular process in which spindle microtubules become physically associated with the proteins making up the kinetochore complex in meiosis.","definition_xrefs":["GOC:dph","GOC:ai","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"attachment of spindle microtubules to kinetochore","termid":"GO:0008608"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"meiotic metaphase chromosome alignment","termid":"GO:0051311"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00418":null,"SJAG_00678":null,"SJAG_00794":null,"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01278":null,"SJAG_01371":null,"SJAG_01775":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02346":null,"SJAG_02731":null,"SJAG_02814":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03327":null,"SJAG_03437":null,"SJAG_03683":null,"SJAG_03926":null,"SJAG_03989":null,"SJAG_04076":null,"SJAG_04508":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05319":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0140013","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"attachment of meiotic spindle microtubules to kinetochore","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0051317"],"synonyms":[{"name":"attachment of spindle microtubules to kinetochore during meiosis","type":"related"},{"name":"attachment of spindle microtubules to kinetochore during meiotic chromosome segregation","type":"related"},{"name":"attachment of spindle microtubules to meiotic chromosome","type":"exact"}],"termid":"GO:0051316","terms_by_termid":{"GO:0051316":null,"GO:0051455":null,"GO:0051456":null,"GO:1904967":null}}


id: PBO:0046248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELOVL fatty acid elongase 4","termid":"PBO:0046248"}


id: GO:0061113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Morphogenesis of the pancreas. Morphogenesis is the process in which anatomical structures are generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"},{"relation_name":"part_of","term_name":"pancreas development","termid":"GO:0031016"}],"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":"pancreas morphogenesis","termid":"GO:0061113"}


id: MONDO:0006778
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign melanocytic nevus with a halo appearance.","definition_xrefs":["NCIT:C7602"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"halo nevus","secondary_identifiers":["ICD9:709.09","MedDRA:10062794","ICDO:8723/0","MESH:D055882","UMLS:C0474824","MEDGEN:141636","EFO:1000958","SCTID:398028009"],"synonyms":[{"name":"halo nevi","type":"exact"},{"name":"leukoderma acquisitum Centrifugum of Sutton","type":"related"}],"termid":"MONDO:0006778","xrefs":{"Monarch":{"xref_id":"0006778"}}}


id: PBO:0079026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-undetermined (NNN) 9-1","termid":"PBO:0079026"}


id: MONDO:1011454
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteogenesis imperfecta that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia, non-human animal","termid":"MONDO:1010306"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteogenesis imperfecta, non-human animal","secondary_identifiers":["OMIA:000754"],"termid":"MONDO:1011454","xrefs":{"Monarch":{"xref_id":"1011454"}}}


id: PBO:0002594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-adenosylmethionine transporter (predicted)","termid":"PBO:0002594"}


id: PBO:0058546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6125","termid":"PBO:0058546"}


id: GO:0045182
data:
  {"annotated_genes":["SJAG_01249","SJAG_01696","SJAG_02390","SJAG_05271","SJAG_05003","SJAG_05332","SJAG_05221","SJAG_03732","SJAG_04981","SJAG_01576","SJAG_01518","SJAG_01117","SJAG_00338","SJAG_02043","SJAG_02180","SJAG_03433","SJAG_04959","SJAG_00308","SJAG_01438","SJAG_04283","SJAG_03788","SJAG_01643","SJAG_02638","SJAG_04744","SJAG_03232","SJAG_04157","SJAG_02189","SJAG_03550","SJAG_03996","SJAG_01079","SJAG_01487","SJAG_00466","SJAG_00662","SJAG_04772","SJAG_01851","SJAG_04891","SJAG_00786","SJAG_02307","SJAG_03147","SJAG_02471","SJAG_01813","SJAG_02493","SJAG_01517","SJAG_02353","SJAG_04635","SJAG_02164","SJAG_03678","SJAG_05000","SJAG_02856","SJAG_03629","SJAG_02995","SJAG_02812","SJAG_01954","SJAG_02601","SJAG_00507","SJAG_03223","SJAG_03472","SJAG_02376","SJAG_02738","SJAG_03461","SJAG_02628","SJAG_01659","SJAG_04900","SJAG_02017"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[116267],"is_not":false,"summary":null,"term":"GO:0045182"},{"annotations":[118352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000900"},{"annotations":[98211,112115,99953,101404,88087,98954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008494"},{"annotations":[94629,116398,97811,117920,117919,114172,117921,118394,118393,94628,108631,93110,111855,112316,94846,111594,102373,111854,111853,108630,93111,93112,97810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003746"},{"annotations":[98432,96167,89876,105059,97889,110153,105078,89417,115063,89454,110067,113421,104794,96738,95375,96089,99997,106487,97293,97313,97232,102122,92279,102700,87044,104237,106778,96358,94295,104891,110793,105087,103542,99598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003743"},{"annotations":[116941,98157,90608,95442,101560,106647,115480],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003747"},{"annotations":[98158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016150"},{"annotations":[90609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016149"},{"annotations":[111607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030371"},{"annotations":[94630,104185,108632,94631,108633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008079"}]},"cv_name":"molecular_function","definition":"Any molecular function involved in the 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":64,"genes_by_uniquename":{"SJAG_00308":null,"SJAG_00338":null,"SJAG_00466":null,"SJAG_00507":null,"SJAG_00662":null,"SJAG_00786":null,"SJAG_01079":null,"SJAG_01117":null,"SJAG_01249":null,"SJAG_01438":null,"SJAG_01487":null,"SJAG_01517":null,"SJAG_01518":null,"SJAG_01576":null,"SJAG_01643":null,"SJAG_01659":null,"SJAG_01696":null,"SJAG_01813":null,"SJAG_01851":null,"SJAG_01954":null,"SJAG_02017":null,"SJAG_02043":null,"SJAG_02164":null,"SJAG_02180":null,"SJAG_02189":null,"SJAG_02307":null,"SJAG_02353":null,"SJAG_02376":null,"SJAG_02390":null,"SJAG_02471":null,"SJAG_02493":null,"SJAG_02601":null,"SJAG_02628":null,"SJAG_02638":null,"SJAG_02738":null,"SJAG_02812":null,"SJAG_02856":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03223":null,"SJAG_03232":null,"SJAG_03433":null,"SJAG_03461":null,"SJAG_03472":null,"SJAG_03550":null,"SJAG_03629":null,"SJAG_03678":null,"SJAG_03732":null,"SJAG_03788":null,"SJAG_03996":null,"SJAG_04157":null,"SJAG_04283":null,"SJAG_04635":null,"SJAG_04744":null,"SJAG_04772":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04959":null,"SJAG_04981":null,"SJAG_05000":null,"SJAG_05003":null,"SJAG_05221":null,"SJAG_05271":null,"SJAG_05332":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},"synonyms":[{"name":"translation factor activity","type":"exact"}],"termid":"GO:0045182","terms_by_termid":{"GO:0000900":null,"GO:0003743":null,"GO:0003746":null,"GO:0003747":null,"GO:0008079":null,"GO:0008494":null,"GO:0016149":null,"GO:0016150":null,"GO:0030371":null,"GO:0045182":null}}


id: PBO:0048104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FtsJ RNA 2'-O-methyltransferase 3","termid":"PBO:0048104"}


id: MONDO:0003988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare lymphoma that arises from the bone or soft tissue of the sternum.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sternum cancer","termid":"MONDO:0003273"},{"relation_name":"is_a","term_name":"primary bone lymphoma","termid":"MONDO:0017814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"sternum lymphoma","secondary_identifiers":["MEDGEN:277770","DOID:6762","NCIT:C6716","UMLS:C1336504"],"synonyms":[{"name":"lymphoma of sternum","type":"exact"},{"name":"lymphoma of the sternum","type":"exact"},{"name":"primary sternal lymphoma","type":"exact"},{"name":"sternal lymphoma","type":"exact"},{"name":"sternum lymphoma","type":"exact"}],"termid":"MONDO:0003988","xrefs":{"Monarch":{"xref_id":"0003988"}}}


id: GO:0019254
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving carnitine, where metabolism is linked to CoA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carnitine metabolic process","termid":"GO:0009437"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"carnitine metabolic process, CoA-linked","secondary_identifiers":["MetaCyc:CARNMET-PWY"],"synonyms":[{"name":"carnitine metabolism, CoA-linked","type":"exact"}],"termid":"GO:0019254"}


id: PBO:0084714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane localized ATP-dependent DNA helicase; required for the maintenance of the mitochondrial genome; not required for mitochondrial transcription; has homology to E. coli helicase uvrD","termid":"PBO:0084714"}


id: PR:O74480
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1840.07c gene.","definition_xrefs":["UniProtKB:O74480","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 C1840.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1840.07c","synonyms":[{"name":"Spom972h-SPCC1840.07c","type":"exact"}],"termid":"PR:O74480"}


id: MONDO:0013537
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CLDN14 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 29","secondary_identifiers":["UMLS:C3279660","DOID:0110487","MEDGEN:481290","OMIM:614035","GARD:22641"],"synonyms":[{"name":"CLDN14 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"DFNB29","type":"narrow"},{"name":"autosomal recessive deafness 29","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 29","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in CLDN14","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 29","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 29","type":"exact"},{"name":"deafness, autosomal recessive 29","type":"narrow"},{"name":"deafness, autosomal recessive type 29","type":"narrow"}],"termid":"MONDO:0013537","xrefs":{"Monarch":{"xref_id":"0013537"}}}


id: PATO:0000174
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000174 autonomic function (obsolete PATO:0000174)","termid":"PATO:0000174"}


id: PBO:0070809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 39","termid":"PBO:0070809"}


id: GO:0007079
data:
  {"annotated_genes":["SJAG_02336","SJAG_01297","SJAG_02761"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99876,103379,107717],"is_not":false,"summary":null,"term":"GO:0007079"}]},"cv_name":"biological_process","definition":"The cell cycle process in which the directed movement of chromosomes from the center of the spindle towards the spindle poles occurs. This mediates by the shortening of microtubules attached to the chromosomes, during mitosis.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome movement towards spindle pole","termid":"GO:0051305"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic sister chromatid segregation","termid":"GO:0000070"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01297":null,"SJAG_02336":null,"SJAG_02761":null},"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"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0000070","GO:0051179"],"is_obsolete":false,"name":"mitotic chromosome movement towards spindle pole","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0007082"],"synonyms":[{"name":"chromosome migration to spindle pole during mitosis","type":"exact"},{"name":"chromosome movement towards spindle pole during mitosis","type":"exact"},{"name":"mitotic chromosome movement","type":"broad"},{"name":"mitotic chromosome movement to spindle pole","type":"exact"},{"name":"mitotic sister chromosome movement towards spindle pole","type":"exact"},{"name":"sister chromosome movement towards spindle pole during mitosis","type":"exact"}],"termid":"GO:0007079","terms_by_termid":{"GO:0007079":null}}


id: GO:0003046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The intrinsic circulatory process resulting from stress relaxation that modulates the force with which blood travels through the systemic arterial circulatory system. Stress relaxation is the adaptation of vessels to a new size as a result of changes in pressure in storage areas such as veins, the liver, the spleen, and the lungs.","definition_xrefs":["GOC:mtg_cardio","ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure by physical factors","termid":"GO:0003045"},{"relation_name":"is_a","term_name":"negative regulation of systemic arterial blood pressure","termid":"GO:0003085"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of systemic arterial blood pressure by stress relaxation","synonyms":[{"name":"blood pressure regulation by stress relaxation","type":"exact"}],"termid":"GO:0003046"}


id: PBO:0004328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-M (predicted)","termid":"PBO:0004328"}


id: MONDO:0018113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Isolated synostotic plagiocephaly (SP) is a form of nonsyndromic craniosynostosis characterized by premature fusion of one coronal suture leading to skull deformity and facial asymmetry.","definition_xrefs":["Orphanet:35098"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"}],"gene_count":0,"genotype_count":0,"name":"obsolete isolated plagiocephaly (obsolete MONDO:0018113)","synonyms":[{"name":"non-syndromic unicoronal synostosis","type":"exact"},{"name":"synostotic plagiocephaly","type":"exact"}],"termid":"MONDO:0018113","xrefs":{"Monarch":{"xref_id":"0018113"}}}


id: MONDO:0020718
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"congenital short bowel syndrome","termid":"MONDO:0014097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"congenital short bowel syndrome, autosomal recessive","secondary_identifiers":["GARD:18585","OMIM:615237"],"synonyms":[{"name":"CSBS","type":"broad"},{"name":"congenital short bowel syndrome","type":"broad"},{"name":"congenital short bowel syndrome 1","type":"exact"},{"name":"congenital short bowel syndrome due to CLMP variation","type":"exact"}],"termid":"MONDO:0020718","xrefs":{"Monarch":{"xref_id":"0020718"}}}


id: GO:0035852
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a horizontal cell is transported to, and/or maintained in, a specific location within the inner nuclear layer (INL) of the retina. A horizontal cell is a neuron that laterally connects other neurons in the inner nuclear layer (INL) of the retina. Targeting of retinal neurons to the appropriate lamina is vital to establish the architecture of the retina.","definition_xrefs":["GOC:bf","GOC:yaf","CL:0000745","PMID:18094249"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localization of cell","termid":"GO:0051674"},{"relation_name":"part_of","term_name":"retina layer formation","termid":"GO:0010842"}],"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:0008150","GO:0051179"],"is_obsolete":false,"name":"horizontal cell localization","synonyms":[{"name":"horizontal cell localisation","type":"exact"},{"name":"horizontal cell positioning","type":"exact"},{"name":"laminar positioning of retinal horizontal cell","type":"exact"},{"name":"retinal horizontal cell positioning","type":"exact"}],"termid":"GO:0035852"}


id: GO:0032672
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-3 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-3 production","termid":"GO:0032632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of interleukin-3 production","secondary_identifiers":["GO:0045399"],"synonyms":[{"name":"regulation of IL-3 production","type":"exact"},{"name":"regulation of interleukin-3 biosynthetic process","type":"narrow"}],"termid":"GO:0032672"}


id: SO:0001977
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a transcript encoding the cleavage site for a ribonuclease enzyme.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_region","termid":"SO:0000833"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease_site","synonyms":[{"name":"ribonuclease site","type":"exact"}],"termid":"SO:0001977"}


id: PBO:0111850
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RecA family","termid":"PBO:0111850"}


id: FYPO:0007353
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which homologous chromosome pairing during meiosis (synapsis) is normal (i.e. indistinguishable from wild type) at a cis-acting homologous chromosome pairing region on chromosome 2.","definition_xrefs":["PMID:31811152","PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal homologous chromosome pairing at cis-acting homologous chromosome pairing region","termid":"FYPO:0003051"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal homologous chromosome pairing at cis-acting homologous chromosome pairing region on chromosome 2","synonyms":[{"name":"normal homologous chromosome pairing at meiosis at cis-acting homologous chromosome pairing region on chromosome 2","type":"exact"},{"name":"normal homologous chromosome pairing at sme2 locus","type":"narrow"},{"name":"normal synapsis at cis-acting homologous chromosome pairing region on chromosome 2","type":"exact"}],"termid":"FYPO:0007353"}


id: GO:0071893
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by the binding of a member of the BMP (bone morphogenetic protein) family to its receptor on the surface of a target cell, which contributes to nephric duct formation.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete BMP signaling pathway involved in nephric duct formation (obsolete GO:0071893)","synonyms":[{"name":"BMP signalling pathway involved in nephric duct formation","type":"exact"}],"termid":"GO:0071893"}


id: GO:0102482
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-deoxy-D-glucuronate = 5-dehydro-2-deoxy-D-gluconate.","definition_xrefs":["RHEA:25840","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"5-deoxy-D-glucuronate isomerase activity","secondary_identifiers":["EC:5.3.1.30","MetaCyc:RXN-14150"],"termid":"GO:0102482"}


id: FYPO:0001521
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of glutathione (GSH) measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular glutathione level during vegetative growth","synonyms":[{"name":"increased cellular GSH level during vegetative growth","type":"exact"},{"name":"increased cellular L-gamma-glutamyl-L-cysteinylglycine level during vegetative growth","type":"exact"},{"name":"increased cellular glutathione level during mitotic cell cycle","type":"related"},{"name":"increased cellular reduced glutathione level during vegetative growth","type":"exact"},{"name":"increased glutathione accumulation during vegetative growth","type":"related"}],"termid":"FYPO:0001521"}


id: PBO:0015213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial pyruvate transmembrane transporter Mpc2 (predicted)","termid":"PBO:0015213"}


id: PBO:0017415
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-derived_into","termid":"PBO:0017415"}


id: PBO:0077804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOX high mobility group box family member 2","termid":"PBO:0077804"}


id: PBO:0091995
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tfb6 annotation seems tenuous, SGD have not annotated","termid":"PBO:0091995"}


id: MONDO:0001828
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Non-heritable difficulty in distinguishing colors.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color vision disorder","termid":"MONDO:0001703"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acquired color blindness","secondary_identifiers":["ICD9:368.55","DOID:13912","MEDGEN:57828","UMLS:C0155018","SCTID:71676008","NCIT:C118712","ICD10CM:H53.52"],"synonyms":[{"name":"acquired color vision deficiencies","type":"exact"},{"name":"acquired color vision deficiency","type":"exact"},{"name":"acquired color vision disorder","type":"exact"},{"name":"acquired colour vision deficiencies","type":"exact"},{"name":"acquired colour vision deficiency","type":"exact"},{"name":"acquired colour vision disorder","type":"exact"}],"termid":"MONDO:0001828","xrefs":{"Monarch":{"xref_id":"0001828"}}}


id: PBO:0065295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 2","termid":"PBO:0065295"}


id: GO:0002071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process, independent of morphogenetic (shape) change, that is required for a glandular epithelial cell to attain its fully functional state. A glandular epithelial cell is a columnar/cuboidal epithelial cell is a cell found in a two dimensional sheet with a free surface exposed to the lumen of a gland.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"columnar/cuboidal epithelial cell maturation","termid":"GO:0002069"},{"relation_name":"part_of","term_name":"glandular epithelial cell development","termid":"GO:0002068"}],"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":"glandular epithelial cell maturation","termid":"GO:0002071"}


id: PBO:0075669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine palmitoyltransferase long chain base subunit 1 pseudogene 4","termid":"PBO:0075669"}


id: MONDO:0008209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Char syndrome is characterized by the triad of patent ductus arteriosus (PDA), facial dysmorphism and hand anomalies.","definition_xrefs":["Orphanet:46627"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"patent ductus arteriosus","termid":"MONDO:0011827"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"}],"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":"Char syndrome","secondary_identifiers":["UMLS:C1868570","OMIM:169100","DOID:0060563","GARD:1237","MESH:C566815","MEDGEN:358356","SCTID:703534001","ICD9:759.89"],"synonyms":[{"name":"CHAR","type":"related"},{"name":"CHAR syndrome","type":"related"},{"name":"Char","type":"related"},{"name":"Char syndrome","type":"exact"},{"name":"patent ductus arteriosus with Facial Dysmorphism and abnormal fifth digits","type":"related"},{"name":"patent ductus arteriosus with facial dysmorphism and abnormal fifth digits","type":"exact"}],"termid":"MONDO:0008209","xrefs":{"Monarch":{"xref_id":"0008209"}}}


id: PBO:0042669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule pseudogene 3","termid":"PBO:0042669"}


id: MONDO:0003489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete middle ear squamous cell carcinoma (obsolete MONDO:0003489)","termid":"MONDO:0003489","xrefs":{"Monarch":{"xref_id":"0003489"}}}


id: GO:0003934
data:
  {"annotated_genes":["SJAG_03275"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89817],"is_not":false,"summary":null,"term":"GO:0003934"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: GTP + H2O = 7,8-dihydroneopterin 3'-triphosphate + formate + H+.","definition_xrefs":["EC:3.5.4.16"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GTP cyclohydrolase activity","termid":"GO:0003933"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03275":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"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:0016810","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"GTP cyclohydrolase I activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:GTP-CYCLOHYDRO-I-RXN","RHEA:17473","KEGG_REACTION:R00424","Reactome:R-HSA-1474146"],"synonyms":[{"name":"GTP 7,8-8,9-dihydrolase activity","type":"related"},{"name":"GTP 8-formylhydrolase activity","type":"related"},{"name":"dihydroneopterin triphosphate synthase activity","type":"related"},{"name":"guanosine triphosphate 8-deformylase activity","type":"related"},{"name":"guanosine triphosphate cyclohydrolase activity","type":"related"}],"termid":"GO:0003934","terms_by_termid":{"GO:0003934":null}}


id: PBO:0059043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multimerin 2","termid":"PBO:0059043"}


id: PATO:0001066
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001066 absolute stiffness (obsolete PATO:0001066)","termid":"PATO:0001066"}


id: GO:0000967
data:
  {"annotated_genes":["SJAG_04524","SJAG_04006","SJAG_00772","SJAG_04767","SJAG_04224","SJAG_02250"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94900],"is_not":false,"summary":null,"term":"GO:0000967"},{"annotations":[107086,99315,108463,114640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000472"},{"annotations":[106919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000465"}]},"cv_name":"biological_process","definition":"Any process involved in forming the mature 5' end of an rRNA molecule.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA 5'-end processing","termid":"GO:0000966"},{"relation_name":"is_a","term_name":"rRNA processing","termid":"GO:0006364"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00772":null,"SJAG_02250":null,"SJAG_04006":null,"SJAG_04224":null,"SJAG_04524":null,"SJAG_04767":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0042254"}],"interesting_parent_ids":["GO:0010467","GO:0042254","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"rRNA 5'-end processing","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"rRNA 5' end processing","type":"exact"}],"termid":"GO:0000967","terms_by_termid":{"GO:0000465":null,"GO:0000472":null,"GO:0000967":null}}


id: PBO:0084198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Histone methyltransferase, subunit of the COMPASS (Set1C) complex; COMPASS methylates histone H3K4; Set1p-dependent H3K4 trimethylation recruits Nrd1p, allowing efficient termination of snoRNAs and cryptic unstable transcripts (CUTs) by Nrd1p-Nab3p-Sen1p pathway; modulates histone acetylation levels in promoter proximal regions to ensure efficient Nrd1p-dependent termination; required in transcriptional silencing near telomeres and at silent mating type loci; has a SET domain","termid":"PBO:0084198"}


id: MONDO:0021495
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the sublingual gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sublingual gland neoplasm","termid":"MONDO:0021242"},{"relation_name":"is_a","term_name":"benign neoplasm of major salivary gland","termid":"MONDO:0021492"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of sublingual gland","secondary_identifiers":["UMLS:C0347208","MEDGEN:83858","NCIT:C4601","SCTID:92413008"],"synonyms":[{"name":"benign neoplasm of the sublingual gland","type":"exact"},{"name":"benign sublingual gland neoplasm","type":"exact"},{"name":"benign sublingual gland tumor","type":"exact"},{"name":"benign sublingual gland tumour","type":"exact"},{"name":"benign tumor of sublingual gland","type":"exact"},{"name":"benign tumor of the sublingual gland","type":"exact"},{"name":"benign tumour of sublingual gland","type":"exact"},{"name":"benign tumour of the sublingual gland","type":"exact"},{"name":"sublingual gland benign neoplasm","type":"exact"}],"termid":"MONDO:0021495","xrefs":{"Monarch":{"xref_id":"0021495"}}}


id: PBO:0058844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8073","termid":"PBO:0058844"}


id: PBO:0063878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol glycan anchor biosynthesis class G","termid":"PBO:0063878"}


id: PBO:0002014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amidohydrolase","termid":"PBO:0002014"}


id: GO:0002241
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 stimulus from a parasitic plant.","definition_xrefs":["PMID:16547862","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to symbiont","termid":"GO:0009608"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to parasitic plant","termid":"GO:0002241"}


id: MONDO:0009756
data:
  {"annotated_genes":["SJAG_00570"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86447],"is_not":false,"summary":null,"term":"MONDO:0009756"}]},"cv_name":"mondo","definition":"Niemann-Pick disease type A is a very severe subtype of Niemann-Pick disease, an autosomal recessive lysosomal disease, and is characterized clinically by onset in infancy or early childhood with failure to thrive, hepatosplenomegaly, and rapidly progressive neurodegenerative disorders.","definition_xrefs":["Orphanet:77292"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"acid sphingomyelinase deficiency","termid":"MONDO:0100464"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00570":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0006025","MONDO:0002561","MONDO:0005328","MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"Niemann-Pick disease type A","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2201206","NANDO:1200061","MESH:D052536","DOID:0070111","GARD:7206","MEDGEN:78650","UMLS:C0268242","icd11.foundation:530611243","OMIM:257200","NCIT:C126561","SCTID:52165006"],"synonyms":[{"name":"Niemann-PICK disease, type A","type":"related"},{"name":"Niemann-Pick disease, Intermediate, protracted neurovisceral","type":"related"},{"name":"sphingomyelin lipidosis","type":"related"},{"name":"sphingomyelinase deficiency","type":"related"}],"termid":"MONDO:0009756","terms_by_termid":{"MONDO:0009756":null},"xrefs":{"Monarch":{"xref_id":"0009756"}}}


id: PBO:0087915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor involved in regulating gluconeogenesis; also involved in the regulation of glyoxylate cycle genes; member of the zinc cluster family of proteins; confers resistance to ketoconazole","termid":"PBO:0087915"}


id: PBO:0079155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TSPAN14 antisense RNA 1","termid":"PBO:0079155"}


id: MONDO:0014906
data:
  {"annotated_genes":["SJAG_00031"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85669],"is_not":false,"summary":null,"term":"MONDO:0014906"}]},"cv_name":"mondo","definition":"An autosomal recessive sub-type of Charcot-Marie-Tooth disease caused by compound heterozygous or homozygous mutation(s) in the MFN2 gene, encoding mitofusin-2. This condition is more severe and has an earlier onset as compared to Charcot-Marie-Tooth disease type 2A2A.","definition_xrefs":["NCIT:C150647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00031":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617087","UMLS:C4310725","MEDGEN:934692","DOID:0111557"],"synonyms":[{"name":"CMT2A2B","type":"related"},{"name":"Charcot-Marie-Tooth disease type 2A2B","type":"exact"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2A2B","type":"exact"}],"termid":"MONDO:0014906","terms_by_termid":{"MONDO:0014906":null},"xrefs":{"Monarch":{"xref_id":"0014906"}}}


id: GO:0106185
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by addition of one or more methyl groups to lysine at position 37 of the histone.","definition_xrefs":["GOC:mah","PMID:30773398"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K37 methylation (obsolete GO:0106185)","synonyms":[{"name":"histone H3 K37 methylation","type":"exact"},{"name":"histone H3K37me","type":"exact"},{"name":"histone lysine H3 K37 methylation","type":"exact"}],"termid":"GO:0106185"}


id: GO:0047454
data:
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id: GO:1902117
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id: FYPO:0000334
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type"}]}]},"ned1delta":{"display_name":"ned1delta","display_uniquename":"ned1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-1","expression":"Null"}]}]},"nem1delta":{"display_name":"nem1delta","display_uniquename":"nem1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01906:allele-1","expression":"Null"}]}]},"nem2delta":{"display_name":"nem2delta","display_uniquename":"nem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03940:allele-1","expression":"Null"}]}]},"nup132delta":{"display_name":"nup132delta","display_uniquename":"nup132delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01374:allele-1","expression":"Null"}]}]},"nup61delta":{"display_name":"nup61delta","display_uniquename":"nup61delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04284:allele-1","expression":"Null"}]}]},"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"ptp4delta":{"display_name":"ptp4delta","display_uniquename":"ptp4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04883:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-1","expression":"Not assayed or wild type"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]},"vps32delta":{"display_name":"vps32delta","display_uniquename":"vps32delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01242:allele-1","expression":"Null"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]},"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"wee1-as8(T582G aa)","display_uniquename":"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_02392","SJAG_01143","SJAG_03596","SJAG_04522","SJAG_04280"],"name":"cellular component organization phenotype","references_by_uniquename":{"PMID:21802294":null,"PMID:24184107":null,"PMID:25318672":null,"PMID:25866389":null,"PMID:26774782":null,"PMID:27059155":null,"PMID:28954740":null,"PMID:30664646":null,"PMID:30726171":null,"PMID:32109380":null,"PMID:32243490":null,"PMID:32915139":null,"PMID:33495454":null,"PMID:33791858":null,"PMID:36695178":null},"single_locus_annotated_genes":["SJAG_04280","SJAG_02392","SJAG_03892","SJAG_01906","SJAG_00426","SJAG_01374","SJAG_05207","SJAG_01242","SJAG_01143","SJAG_02592","SJAG_04703","SJAG_03940","SJAG_03449","SJAG_04284","SJAG_02763","SJAG_03596","SJAG_01745","SJAG_03891","SJAG_04464","SJAG_04522","SJAG_04883"],"single_locus_genotype_uniquenames":["man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","man1delta","cmp7delta","vps32delta","nem1delta","ned1cat-D422E,D424E-amino_acid_mutation-expression-not_assayed_or_wild_type","mid1delta","pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","rga4delta","ptp4delta","ned1-5A-S499A__S538A__T620A__T638A__S651A-amino_acid_mutation-expression-not_assayed_or_wild_type","wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","lem2delta","nup132delta","sty1delta","cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type","for3delta","nem2delta","ned1S235A_S651-S235A__S651-amino_acid_mutation-expression-not_assayed_or_wild_type","ned1delta","pom1delta","ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","alx1delta","vps4delta","nup61delta","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type","ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"cellular 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id: MONDO:0018072
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare congenital cardiovascular disorder characterized by the failure of the embryologic structure truncus arteriosus to divide into the aorta and pulmonary trunk. It results in the presence of a single vessel instead of two vessels leading out of the heart. Clinical signs and symptoms include cyanosis that is present at birth, poor growth, dyspnea, tachypnea, arrhythmia, cardiomegaly, and heart failure. If it is not surgically repaired, it leads to death.","definition_xrefs":["NCIT:C98880"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete genetic cardiac malformation (obsolete MONDO:0018797)","termid":"MONDO:0018797"},{"relation_name":"is_a","term_name":"congenital heart disease","termid":"MONDO:0005453"},{"relation_name":"is_a","term_name":"conotruncal heart malformations","termid":"MONDO:0016581"}],"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":"persistent truncus arteriosus","secondary_identifiers":["MESH:D014339","UMLS:C0041207","Orphanet:3384","NANDO:2200261","NANDO:1200693","icd11.foundation:1832500366","GARD:16627","MEDGEN:52867","NORD:1800"],"synonyms":[{"name":"TAC","type":"exact"},{"name":"Truncus Arteriosus","type":"exact"},{"name":"common aorticopulmonary trunk","type":"exact"},{"name":"common arterial trunk","type":"exact"},{"name":"common truncus arteriosus","type":"exact"},{"name":"persistent truncus arteriosus","type":"exact"},{"name":"persistent truncus arteriosus (disease)","type":"exact"},{"name":"truncus arteriosus","type":"exact"}],"termid":"MONDO:0018072","xrefs":{"Monarch":{"xref_id":"0018072"}}}


id: PBO:0086683
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; identified by homology to <i>Ashbya gossypii</i>","termid":"PBO:0086683"}


id: GO:0036206
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of expression of a histone-encoding gene. Gene expression is the process in which a gene's coding sequence is converted into a mature gene product or products (proteins or RNA). This includes the production of an RNA transcript as well as any processing to produce a mature RNA product or an mRNA (for protein-coding genes) and the translation of that mRNA into protein.","definition_xrefs":["GOC:krc","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone gene expression (obsolete GO:0036206)","synonyms":[{"name":"regulation of expression of histone-encoding gene","type":"exact"}],"termid":"GO:0036206"}


id: PBO:0065348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRXL2C pseudogene 1","termid":"PBO:0065348"}


id: GO:0030784
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + 3'-hydroxy-N-methyl-(S)-coclaurine = S-adenosyl-L-homocysteine + (S)-reticuline.","definition_xrefs":["EC:2.1.1.116"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016741","GO:0003674"],"is_obsolete":false,"name":"3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase activity","secondary_identifiers":["RHEA:17789","MetaCyc:2.1.1.116-RXN"],"synonyms":[{"name":"S-adenosyl-L-methionine:3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase activity","type":"related"}],"termid":"GO:0030784"}


id: PBO:0045813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 3","termid":"PBO:0045813"}


id: PBO:0042348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD83 molecule","termid":"PBO:0042348"}


id: PBO:0012241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial pyrimidine nucleotide transporter (predicted)","termid":"PBO:0012241"}


id: SO:0000013
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A small non coding RNA sequence, present in the cytoplasm.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"scRNA_primary_transcript","termid":"SO:0000012"},{"relation_name":"is_a","term_name":"ncRNA","termid":"SO:0000655"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scRNA","synonyms":[{"name":"INSDC_feature:ncRNA","type":"broad"},{"name":"INSDC_qualifier:scRNA","type":"exact"},{"name":"small cytoplasmic RNA","type":"exact"}],"termid":"SO:0000013"}


id: FYPO:0003316
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the growing cell tip is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to cell tip during vegetative growth","termid":"FYPO:0001587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000138","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to growing cell tip","synonyms":[{"name":"normal protein localisation to growing cell tip","type":"exact"},{"name":"normal protein localization to growing cell end","type":"exact"},{"name":"normal protein localization to growing cell tip during mitotic cell cycle","type":"related"},{"name":"normal protein localization to growing cell tip during vegetative growth","type":"exact"}],"termid":"FYPO:0003316"}


id: PBO:0012889
data:
  {"annotation_feature_type":"gene","cv_name":"feature_cvtermprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"quant_gene_ex_cell_distribution","termid":"PBO:0012889"}


id: GO:0050589
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: leucocyanidin + 2-oxoglutarate + O2 = cis- or trans-dihydroquercetin + succinate + CO2 + 2 H2O.","definition_xrefs":["EC:1.14.20.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"leucocyanidin oxygenase activity","secondary_identifiers":["GO:0045432","MetaCyc:RXN-602"],"synonyms":[{"name":"anthocyanidin synthase activity","type":"related"},{"name":"leucoanthocyanidin dioxygenase activity","type":"related"},{"name":"leucoanthocyanidin hydroxylase","type":"related"},{"name":"leucocyanidin,2-oxoglutarate:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0050589"}


id: GO:1990100
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex containing homohexameric DNA helicase DnaB, and the DNA helicase loader DnaC. The helicase loader DnaC delivers DnaB to the chromosomal origin (oriC).","definition_xrefs":["GOC:bhm","PMID:20129058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"primosome complex","termid":"GO:1990077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0032991","GO:0005694","GO:0005575"],"is_obsolete":false,"name":"DnaB-DnaC complex","synonyms":[{"name":"DnaB6-DnaC3 complex","type":"narrow"},{"name":"DnaB6-DnaC6 complex","type":"narrow"},{"name":"helicase-loading complex","type":"broad"}],"termid":"GO:1990100"}


id: PBO:0086422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative GTPase with a role in biogenesis of RNA pol II and polIII; may be involved in assembly of RNA polymerases II and III and in their transport into the nucleus; may have a role in sister chromatid cohesion; SWAT-GFP and mCherry fusion proteins localize to the endoplasmic reticulum and vacuole respectively; contains a Gly-Pro-Asn motif in the G domain; similar to Npa3p and Gpn2p","termid":"PBO:0086422"}


id: GO:0008936
data:
  {"annotated_genes":["SJAG_04467"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[109079],"is_not":false,"summary":null,"term":"GO:0008936"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: nicotinamide + H2O = nicotinate + NH3.","definition_xrefs":["RHEA:14545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amidase activity","termid":"GO:0004040"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04467":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0016810","GO:0003674"],"is_obsolete":false,"name":"nicotinamidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:3.5.1.19","MetaCyc:NICOTINAMID-RXN"],"synonyms":[{"name":"NAMase activity","type":"related"},{"name":"YNDase activity","type":"related"},{"name":"nicotinamide amidase activity","type":"related"},{"name":"nicotinamide amidohydrolase activity","type":"related"},{"name":"nicotinamide deaminase activity","type":"related"},{"name":"nicotine deamidase activity","type":"related"}],"termid":"GO:0008936","terms_by_termid":{"GO:0008936":null}}


id: GO:0009426
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the central rod of the bacterial-type flagellar basal body that is distal to the cell membrane; spans most of the distance between the inner and outer membranes.","definition_xrefs":["GOC:cilia","GOC:mtg_sensu","PMID:10572114","PMID:11133968","PMID:12624192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"bacterial-type flagellum basal body, rod","termid":"GO:0030694"}],"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":"bacterial-type flagellum basal body, distal rod","synonyms":[{"name":"flagellar basal body, distal rod","type":"exact"},{"name":"flagellin-based flagellum basal body, distal rod","type":"exact"}],"termid":"GO:0009426"}


id: PBO:0055558
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 2994","termid":"PBO:0055558"}


id: GO:0005208
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 amyloid protein (obsolete GO:0005208)","synonyms":[{"name":"amyloid protein","type":"exact"}],"termid":"GO:0005208"}


id: PBO:0004115
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.2.1.1","termid":"PBO:0004115"}


id: SO:0001501
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A collection of peptide sequences.","definition_xrefs":["BBOP:nlw"],"direct_ancestors":[{"relation_name":"has_part","term_name":"polypeptide","termid":"SO:0000104"},{"relation_name":"is_a","term_name":"sequence_collection","termid":"SO:0001260"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptide_collection","synonyms":[{"name":"peptide collection","type":"exact"},{"name":"peptide set","type":"exact"}],"termid":"SO:0001501"}


id: PBO:0069104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 352, pseudogene","termid":"PBO:0069104"}


id: PBO:0054288
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 1679","termid":"PBO:0054288"}


id: PR:P13681
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dis2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P13681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine-protein phosphatase PP1-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC776.02c","synonyms":[{"name":"Spom972h-dis2","type":"exact"}],"termid":"PR:P13681"}


id: MONDO:0016193
data:
  {"annotated_genes":["SJAG_03379","SJAG_04887","SJAG_03145","SJAG_03025"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008070"},{"annotations":[84691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012239"},{"annotations":[86251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009725"},{"annotations":[85396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012538"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"}],"gene_count":4,"genes_by_uniquename":{"SJAG_03025":null,"SJAG_03145":null,"SJAG_03379":null,"SJAG_04887":null},"genotype_count":0,"is_obsolete":false,"name":"qualitative or quantitative defects of alpha-actin","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1842305","Orphanet:209059","GARD:20432","UMLS:C5680845"],"termid":"MONDO:0016193","terms_by_termid":{"MONDO:0008070":null,"MONDO:0009725":null,"MONDO:0012239":null,"MONDO:0012538":null},"xrefs":{"Monarch":{"xref_id":"0016193"}}}


id: PBO:0000482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A) binding protein Nab3 (predicted)","termid":"PBO:0000482"}


id: MONDO:0011707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete familial dyskinesia and facial myokymia (obsolete MONDO:0011707)","termid":"MONDO:0011707","xrefs":{"Monarch":{"xref_id":"0011707"}}}


id: PBO:0074118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 30 member 4","termid":"PBO:0074118"}


id: PBO:0046913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity E5","termid":"PBO:0046913"}


id: GO:0072184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the renal vesicle progenitor cells of the kidney as it progresses from its formation to the mature state. A renal vesicle progenitor cell is a cell that will give rise to terminally differentiated cells of the renal vesicle without self-renewing.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation involved in kidney development","termid":"GO:0061005"},{"relation_name":"part_of","term_name":"renal vesicle development","termid":"GO:0072087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal vesicle progenitor cell differentiation","termid":"GO:0072184"}


id: MONDO:1012272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thrombasthenia, non-human animal","termid":"MONDO:1011694"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombasthenia, horse","secondary_identifiers":["OMIA:001000-9796"],"termid":"MONDO:1012272","xrefs":{"Monarch":{"xref_id":"1012272"}}}


id: PBO:0053578
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 601","termid":"PBO:0053578"}


id: PBO:0052822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 88, pseudogene","termid":"PBO:0052822"}


id: PBO:0065410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome subunit alpha 7 pseudogene 1","termid":"PBO:0065410"}


id: GO:1905160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of Factor XII activation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:617517"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of Factor XII activation (obsolete GO:1905160)","synonyms":[{"name":"activation of Factor XII activation","type":"narrow"},{"name":"activation of Hageman factor activation","type":"narrow"},{"name":"positive regulation of Hageman factor activation","type":"exact"},{"name":"up regulation of Factor XII activation","type":"exact"},{"name":"up regulation of Hageman factor activation","type":"exact"},{"name":"up-regulation of Factor XII activation","type":"exact"},{"name":"up-regulation of Hageman factor activation","type":"exact"},{"name":"upregulation of Factor XII activation","type":"exact"},{"name":"upregulation of Hageman factor activation","type":"exact"}],"termid":"GO:1905160"}


id: PBO:0045617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 28 (pseudogene)","termid":"PBO:0045617"}


id: PBO:0012845
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by H. sapiens SHFM1","termid":"PBO:0012845"}


id: MOD:01233
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to 3x(2)H labeled N6-acetyl-L-lysine.","definition_xrefs":["Unimod:56#K","PubMed:11999733","PubMed:12175151","PubMed:11857757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N6-acetyl-L-lysine","termid":"MOD:00064"},{"relation_name":"is_a","term_name":"acetate labeling reagent (N-term) (heavy form, +3amu)","termid":"MOD:00449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"},{"rel_name":"is_a","termid":"MOD:00408"}],"interesting_parent_ids":["MOD:00408","MOD:01875"],"is_obsolete":false,"name":"3x(2)H labeled N6-acetyl-L-lysine","synonyms":[{"name":"Acetate labeling reagent (N-term & K) (heavy form, +3amu)","type":"related"},{"name":"Acetyl:2H(3)","type":"related"}],"termid":"MOD:01233"}


id: MONDO:0019380
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute arboviral infection caused by an alphavirus of the Togaviridae family transmitted by an infected mosquito, that more frequently affects children and that is characterized by the presence of mild flulike symptoms (fever, chills, headache, nausea, vomiting, and anorexia) but that can progress to weakness, altered mental status, photophobia, mental confusion, seizures, somnolence, coma and/or even death. The disease can leave neurological sequelae, mainly in infants and children, such as seizures, spasticity or behavioral disorders.","definition_xrefs":["Orphanet:83593"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Alphavirus infectious disease","termid":"MONDO:0005643"},{"relation_name":"is_a","term_name":"mosquito-borne viral encephalitis","termid":"MONDO:0020601"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"western equine encephalitis","secondary_identifiers":["GARD:7888","ICD10CM:A83.1","ICD9:062.1","MEDGEN:57778","EFO:0007546","MedDRA:10014614","SCTID:47523006","MESH:D020241","icd11.foundation:1543765035","NCIT:C85227","DOID:10843","UMLS:C0153064"],"synonyms":[{"name":"WEE","type":"related"},{"name":"Western equine encephalitis virus caused infectious encephalitis","type":"exact"},{"name":"Western equine encephalitis virus infectious encephalitis","type":"exact"},{"name":"Western equine encephalomyelitis","type":"exact"}],"termid":"MONDO:0019380","xrefs":{"Monarch":{"xref_id":"0019380"}}}


id: GO:0106174
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a phagolysosome.","definition_xrefs":["PMID:29471269","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuolar lumen","termid":"GO:0005775"},{"relation_name":"is_a","term_name":"cytoplasmic vesicle lumen","termid":"GO:0060205"},{"relation_name":"is_a","term_name":"phagocytic vesicle lumen","termid":"GO:0097013"},{"relation_name":"part_of","term_name":"phagolysosome","termid":"GO:0032010"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005773","GO:0005737"],"is_obsolete":false,"name":"phagolysosome vesicle lumen","termid":"GO:0106174"}


id: PBO:0001487
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Telomere-associated in Yarrowia lipolytica","termid":"PBO:0001487"}


id: GO:0045336
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A clathrin-coated, membrane-bounded intracellular vesicle that arises from the ingestion of particulate material by phagocytosis.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-coated endocytic vesicle","termid":"GO:0045334"},{"relation_name":"is_a","term_name":"phagocytic vesicle","termid":"GO:0045335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0031410","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"clathrin-coated phagocytic vesicle","synonyms":[{"name":"clathrin-coated phagosome","type":"exact"}],"termid":"GO:0045336"}


id: MONDO:0007720
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":"hernia, double inguinal","secondary_identifiers":["OMIM:142350","MEDGEN:163567","MESH:C563164","UMLS:C0860251"],"synonyms":[{"name":"hernia, double inguinal","type":"exact"}],"termid":"MONDO:0007720","xrefs":{"Monarch":{"xref_id":"0007720"}}}


id: PBO:0072232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 7","termid":"PBO:0072232"}


id: MONDO:0007175
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":"PR interval, variation in","secondary_identifiers":["MEDGEN:463601","OMIM:108980","UMLS:C3152251"],"synonyms":[{"name":"Atrioventricular conduction time, variation in","type":"related"},{"name":"PR interval, variation in","type":"exact"},{"name":"PR interval, variation type in","type":"exact"}],"termid":"MONDO:0007175","xrefs":{"Monarch":{"xref_id":"0007175"}}}


id: MONDO:0018592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cutaneous polyarteritis nodosa (CPAN) is a rare limited form of polyarteritis nodosa (PAN), characterized by cutaneous vasculitis and mild and transient extracutaneous manifestations such as mild arthralgia, arthritis,myalgia, and rarely peripheral neuropathy.","definition_xrefs":["Orphanet:439729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary polyarteritis nodosa","termid":"MONDO:0018593"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cutaneous polyarteritis nodosa","secondary_identifiers":["NCIT:C117295","ICD9:709.8","UMLS:C0343190","MEDGEN:83358","GARD:7415","icd11.foundation:1752423171","SCTID:239926000"],"synonyms":[{"name":"cutaneous PAN","type":"exact"},{"name":"cutaneous periarteritis nodosa","type":"exact"}],"termid":"MONDO:0018592","xrefs":{"Monarch":{"xref_id":"0018592"}}}


id: PBO:0064512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit J4, pseudogene","termid":"PBO:0064512"}


id: PBO:0065866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB23, member RAS oncogene family","termid":"PBO:0065866"}


id: GO:1901069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of guanosine-containing compounds (guanosines).","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleoside catabolic process","termid":"GO:0046130"},{"relation_name":"is_a","term_name":"guanosine-containing compound metabolic process","termid":"GO:1901068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"guanosine-containing compound catabolic process","synonyms":[{"name":"guanosine-containing compound breakdown","type":"exact"},{"name":"guanosine-containing compound catabolism","type":"exact"},{"name":"guanosine-containing compound degradation","type":"exact"},{"name":"guanosines breakdown","type":"exact"},{"name":"guanosines catabolic process","type":"exact"},{"name":"guanosines catabolism","type":"exact"},{"name":"guanosines degradation","type":"exact"}],"termid":"GO:1901069"}


id: MONDO:0005648
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dysfunction of the aortic valve characterized by incomplete valve closure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aortic valve disorder","termid":"MONDO:0003803"},{"relation_name":"is_a","term_name":"vascular insufficiency disorder","termid":"MONDO:0020674"}],"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":"aortic valve insufficiency","secondary_identifiers":["EFO:0007148","ICD10CM:I06.1","UMLS:C0003504","ICD9:395.1","MEDGEN:8153","icd11.foundation:1548485475","ICD9:396.3","MESH:D001022","SCTID:78031003","NANDO:2200307","DOID:57","NCIT:C51223"],"synonyms":[{"name":"Corrigan's disease","type":"related"},{"name":"aortic incompetence","type":"exact"},{"name":"aortic insufficiency","type":"exact"},{"name":"aortic regurgitation","type":"exact"},{"name":"rheumatic aortic insufficiency","type":"exact"},{"name":"rheumatic aortic regurgitation","type":"exact"},{"name":"rheumatic aortic valve insufficiency","type":"exact"},{"name":"rheumatic aortic valve regurgitation","type":"exact"}],"termid":"MONDO:0005648","xrefs":{"Monarch":{"xref_id":"0005648"}}}


id: PBO:0057815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3135b","termid":"PBO:0057815"}


id: PBO:0075278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 19 pseudogene 3","termid":"PBO:0075278"}


id: GO:0036370
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding a D-alanine and presenting it for processing or offloading to a cognate enzyme. Covalently binds the D-alanine via a phosphopantetheine prosthetic group and mediates protein-protein interactions with the enzyme conferring specificity. The carrier protein provides an essential link between the D-alanine-D-alanyl carrier protein ligase and the incorporation of D-alanine into lipoteichoic acid by transferring activated D-alanine to cell membrane phosphatidylglycerol (PG).","definition_xrefs":["GOC:crds","PMID:11222605","PMID:22750871","PMID:8682792"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphopantetheine-dependent carrier activity","termid":"GO:0140414"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140104"}],"interesting_parent_ids":["GO:0003674","GO:0140104"],"is_obsolete":false,"name":"D-alanyl carrier activity","synonyms":[{"name":"D-alanyl carrier protein","type":"related"}],"termid":"GO:0036370"}


id: PBO:0066541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of G protein signaling 6","termid":"PBO:0066541"}


id: MONDO:0018392
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete male infertility with spermatogenesis disorder due to single gene mutation (obsolete MONDO:0018392)","secondary_identifiers":["Orphanet:399786"],"termid":"MONDO:0018392","xrefs":{"Monarch":{"xref_id":"0018392"}}}


id: GO:0044484
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process which begins with venom being forced into an organism by the bite or sting of another organism, and ends with fibrinolysis, a process that solubilizes fibrin, chiefly by the proteolytic action of plasmin, in the bloodstream of the bitten/stung organism.","definition_xrefs":["PMID:17544404","GOC:fj","GOC:jl","PMID:17433397"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in impairment of hemostasis in another organism","termid":"GO:0044483"}],"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":"envenomation resulting in fibrinolysis in another organism","synonyms":[{"name":"envenomation resulting in fibrinolysis in other organism","type":"exact"}],"termid":"GO:0044484"}


id: PBO:0072917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scavenger receptor class B member 2","termid":"PBO:0072917"}


id: MOD:00119
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links an L-cysteine residue and an L-serine residue by a thioether bond to form L-lanthionine.","definition_xrefs":["DeltaMass:7","RESID:AA0110#CSX","ChEBI:21347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"L-lanthionine","termid":"MOD:01839"},{"relation_name":"is_a","term_name":"crosslinked L-serine residue","termid":"MOD:02055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-lanthionine (Cys-Ser)","synonyms":[{"name":"(2R,2'R)-3,3'-sulfanediylbis(2-aminopropanoic acid)","type":"exact"},{"name":"(R)-S-(2-amino-2-carboxyethyl)-L-cysteine","type":"exact"},{"name":"(R,R)-2,6-diamino-4-thiaheptanedioic acid","type":"exact"},{"name":"(R,R)-3,3'-thiobis-(2-aminopropanoic acid)","type":"exact"},{"name":"(R,R)-bis(2-amino-2-carboxyethyl)sulfide","type":"exact"},{"name":"2-amino-3-(2-amino-2-carboxyethyl)sulfanylpropanoic acid","type":"exact"},{"name":"3,3'-thiobis-L-alanine","type":"exact"},{"name":"L-lanthionine","type":"exact"},{"name":"XLNK-SCys-(L)3Dha","type":"exact"}],"termid":"MOD:00119"}


id: MONDO:0003199
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the anus","direct_ancestors":[{"relation_name":"is_a","term_name":"anus cancer","termid":"MONDO:0001879"},{"relation_name":"is_a","term_name":"rectal carcinoma","termid":"MONDO:0044937"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"anal carcinoma","secondary_identifiers":["DOID:4908","MEDGEN:76006","SCTID:448315008","NCIT:C9291","UMLS:C0279637"],"synonyms":[{"name":"Ca anus","type":"broad"},{"name":"anal cancer","type":"broad"},{"name":"anal carcinoma","type":"exact"},{"name":"anus carcinoma","type":"exact"},{"name":"cancer of anus","type":"broad"},{"name":"cancer of the anus","type":"broad"},{"name":"carcinoma of anus","type":"exact"},{"name":"carcinoma of the anus","type":"exact"}],"termid":"MONDO:0003199","xrefs":{"Monarch":{"xref_id":"0003199"}}}


id: GO:0060324
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a face from an initial condition to its mature state. The face is the ventral division of the head.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"head development","termid":"GO:0060322"}],"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":"face development","termid":"GO:0060324"}


id: PBO:0039016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"afamin","termid":"PBO:0039016"}


id: PBO:0031883
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae RBL2","termid":"PBO:0031883"}


id: PBO:0074350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"somatomedin B domain containing 1, pseudogene","termid":"PBO:0074350"}


id: PBO:0076471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAF family member associated NFKB activator","termid":"PBO:0076471"}


id: SO:0000332
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Coding region of sequence similarity by descent from a common ancestor.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"conserved_region","termid":"SO:0000330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coding_conserved_region","synonyms":[{"name":"coding conserved region","type":"exact"}],"termid":"SO:0000332"}


id: GO:0004335
data:
  {"annotated_genes":["SJAG_02950"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[113173],"is_not":false,"summary":null,"term":"GO:0004335"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-galactose + ATP = alpha-D-galactose 1-phosphate + ADP + 2 H+.","definition_xrefs":["RHEA:13553","EC:2.7.1.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"carbohydrate kinase activity","termid":"GO:0019200"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02950":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:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016301","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"galactokinase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5610026","KEGG_REACTION:R01092","MetaCyc:GALACTOKIN-RXN","Reactome:R-HSA-70355"],"synonyms":[{"name":"ATP:D-galactose 1-phosphotransferase activity","type":"related"},{"name":"ATP:D-galactose-1-phosphotransferase activity","type":"related"},{"name":"galactokinase (phosphorylating)","type":"related"}],"termid":"GO:0004335","terms_by_termid":{"GO:0004335":null}}


id: PBO:0030396
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_nucleus:cytoplasm_ratio","termid":"PBO:0030396"}


id: PBO:0002243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UPF0103 family","termid":"PBO:0002243"}


id: MONDO:0014465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the CCDC151 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 30","secondary_identifiers":["MEDGEN:863453","OMIM:616037","GARD:16052","DOID:0110624","UMLS:C4015016"],"synonyms":[{"name":"CCDC151 primary ciliary dyskinesia","type":"exact"},{"name":"CILD30","type":"exact"},{"name":"ciliary dyskinesia, primary, 30","type":"related"},{"name":"ciliary dyskinesia, primary, 30, with or without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 30","type":"exact"},{"name":"primary ciliary dyskinesia 30 without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in CCDC151","type":"exact"},{"name":"primary ciliary dyskinesia type 30","type":"exact"}],"termid":"MONDO:0014465","xrefs":{"Monarch":{"xref_id":"0014465"}}}


id: MONDO:0014644
data:
  {"annotated_genes":["SJAG_02306"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84643],"is_not":false,"summary":null,"term":"MONDO:0014644"}]},"cv_name":"mondo","definition":"Autosomal recessive spastic paraplegia type 74 is a rare, genetic, spastic paraplegia-optic atrophy-neuropathy-related (SPOAN-like) disorder characterized by childhood onset of mild to moderate spastic paraparesis which manifests with gait impairment that very slowly progresses into late adulthood, hyperactive patellar reflex and bilateral extensor plantar response, in association with optic atrophy and typical symptoms of peripheral neuropathy, including reduced or absent ankle reflexes, lower limb atrophy and distal sensory impairment. Reduced visual acuity and pes cavus are frequently reported.","definition_xrefs":["Orphanet:468661"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02306":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 74","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:17842","DOID:0110819","MEDGEN:1800260","OMIM:616451","UMLS:C5568837"],"synonyms":[{"name":"IBA57 hereditary spastic paraplegia","type":"exact"},{"name":"SPG74","type":"exact"},{"name":"autosomal recessive spastic paraplegia 74","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 74","type":"related"},{"name":"hereditary spastic paraplegia caused by mutation in IBA57","type":"exact"},{"name":"hereditary spastic paraplegia type 74","type":"exact"},{"name":"spastic paraplegia 74, autosomal recessive","type":"related"}],"termid":"MONDO:0014644","terms_by_termid":{"MONDO:0014644":null},"xrefs":{"Monarch":{"xref_id":"0014644"}}}


id: PBO:0057032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 127","termid":"PBO:0057032"}


id: PBO:0087437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit E of the V1 domain of the vacuolar H+-ATPase (V-ATPase); V-ATPase is an electrogenic proton pump found throughout the endomembrane system; V1 domain has eight subunits; required for the V1 domain to assemble onto the vacuolar membrane; protein abundance increases in response to DNA replication stress","termid":"PBO:0087437"}


id: FYPO:0003492
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of beta-glucanase, any enzyme that degrades cell wall polysaccharides by hydrolyzing beta-glucan linkages, than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0000003","FYPO:0005447","FYPO:0001985","FYPO:0002682"],"is_obsolete":false,"name":"resistance to beta-glucanase","synonyms":[{"name":"resistance to beta-glucanase during mitotic cell cycle","type":"related"},{"name":"resistance to beta-glucanase during vegetative growth","type":"exact"},{"name":"resistant to beta-glucanase","type":"exact"}],"termid":"FYPO:0003492"}


id: GO:1900900
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of heptadecane metabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of metabolic process","termid":"GO:0009892"},{"relation_name":"is_a","term_name":"regulation of heptadecane metabolic process","termid":"GO:1900899"},{"relation_name":"negatively_regulates","term_name":"heptadecane metabolic process","termid":"GO:1900635"}],"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 heptadecane metabolic process","synonyms":[{"name":"down regulation of heptadecane metabolic process","type":"exact"},{"name":"down regulation of heptadecane metabolism","type":"related"},{"name":"down-regulation of heptadecane metabolic process","type":"exact"},{"name":"down-regulation of heptadecane metabolism","type":"related"},{"name":"downregulation of heptadecane metabolic process","type":"exact"},{"name":"downregulation of heptadecane metabolism","type":"related"},{"name":"inhibition of heptadecane metabolic process","type":"narrow"},{"name":"inhibition of heptadecane metabolism","type":"narrow"},{"name":"negative regulation of heptadecane metabolism","type":"related"}],"termid":"GO:1900900"}


id: PBO:0041953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil and C2 domain containing 1A","termid":"PBO:0041953"}


id: PBO:0087528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of NuA4, an essential histone acetyltransferase complex; positions Piccolo NuA4 for efficient acetylation of histone H4 or histone H2A; relocalizes to the cytosol in response to hypoxia; similar to human tumor suppressor ING1 and its isoforms ING4 and ING5","termid":"PBO:0087528"}


id: GO:0102506
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cyanidin 3-O-beta-D-glucoside betaine + 1-O-feruloyl-beta-D-glucose = cyanin betaine + ferulate + H+.","definition_xrefs":["RHEA:35427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016757"],"is_obsolete":false,"name":"cyanidin 3-O-glucoside 5-O-glucosyltransferase (acyl-glucose) activity","secondary_identifiers":["EC:2.4.1.299","KEGG_REACTION:R10261","MetaCyc:RXN-13967"],"termid":"GO:0102506"}


id: GO:0002468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a dendritic cell expresses antigen (peptide or lipid) on its cell surface in association with an MHC protein complex.","definition_xrefs":["PMID:15771591","GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation","termid":"GO:0019882"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"dendritic cell antigen processing and presentation","termid":"GO:0002468"}


id: GO:0071562
data:
  {"annotated_genes":["SJAG_00029"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108885],"is_not":false,"summary":null,"term":"GO:0071562"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a nucleus-vacuole junction (NVJ), membrane contact sites formed between the vacuole membrane and the outer nuclear membrane. In S. cerevisiae these contacts are mediated through direct physical interaction between Vac8p and Nvj1p. The NVJ plays roles in piecemeal microautophagy of the nucleus and in the cytoplasm-to-vacuole targeting pathway.","definition_xrefs":["PMID:28533415","PMID:16709156","GOC:jp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"organelle localization by membrane tethering","termid":"GO:0140056"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00029":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0140056"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0140056","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"nucleus-vacuole junction assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"NV junction assembly","type":"exact"},{"name":"NV junction formation","type":"exact"},{"name":"NVJ assembly","type":"exact"},{"name":"NVJ formation","type":"exact"},{"name":"nucleus-vacuole junction formation","type":"exact"}],"termid":"GO:0071562","terms_by_termid":{"GO:0071562":null}}


id: PBO:0049974
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIG1 hypoxia inducible domain family member 1C","termid":"PBO:0049974"}


id: GO:0008065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment of the barrier between the perineurium of peripheral nerves and the vascular endothelium of endoneurial capillaries. The perineurium acts as a diffusion barrier, but ion permeability at the blood-nerve barrier is still higher than at the blood-brain barrier.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell development","termid":"GO:0001885"},{"relation_name":"part_of","term_name":"peripheral nervous system development","termid":"GO:0007422"}],"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":"establishment of blood-nerve barrier","synonyms":[{"name":"establishment of blood/nerve barrier","type":"exact"}],"termid":"GO:0008065"}


id: PATO:0000397
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000397 slight (obsolete PATO:0000397)","termid":"PATO:0000397"}


id: FYPO:0004696
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to one or more fatty acids (usually supplied as the corresponding anions). Cells stop growing (and may die) at a concentration of fatty acid that allows wild type cells to grow.","definition_xrefs":["PMID:12963726","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:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0000139","FYPO:0001985","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to fatty acid","synonyms":[{"name":"hypersensitive to fatty acid","type":"exact"},{"name":"sensitive to fatty acid anion","type":"exact"},{"name":"sensitive to fatty acid during mitotic cell cycle","type":"related"},{"name":"sensitive to fatty acid during vegetative growth","type":"exact"},{"name":"sensitive to free fatty acids","type":"exact"}],"termid":"FYPO:0004696"}


id: GO:0036480
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals in which an intracellular signal is conveyed to trigger the apoptotic death of a neuron. The pathway is induced in response to oxidative stress, a state often resulting from exposure to high levels of reactive oxygen species, and ends when the execution phase of apoptosis is triggered.","definition_xrefs":["GOC:PARL","PMID:23858059","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intrinsic apoptotic signaling pathway in response to oxidative stress","termid":"GO:0008631"},{"relation_name":"part_of","term_name":"neuron apoptotic process","termid":"GO:0051402"}],"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:0008150","GO:0023052"],"is_obsolete":false,"name":"neuron intrinsic apoptotic signaling pathway in response to oxidative stress","synonyms":[{"name":"neuron apoptosis in response to oxidative stress","type":"related"},{"name":"oxidative stress-induced neuron apoptosis","type":"broad"},{"name":"oxidative stress-induced neuronal apoptosis","type":"broad"}],"termid":"GO:0036480"}


id: MONDO:1010801
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Brachydactyly that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brachydactyly, non-human animal","termid":"MONDO:1010156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly, dog","secondary_identifiers":["OMIA:000146-9615"],"termid":"MONDO:1010801","xrefs":{"Monarch":{"xref_id":"1010801"}}}


id: GO:0170020
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of an ion by a channel that opens when a specific odorant has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["PMID:24661599","PMID:21857978"],"direct_ancestors":[{"relation_name":"is_a","term_name":"olfactory receptor activity","termid":"GO:0004984"},{"relation_name":"is_a","term_name":"ligand-gated monoatomic ion channel activity","termid":"GO:0015276"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674","GO:0038023"],"is_obsolete":false,"name":"ionotropic olfactory receptor activity","termid":"GO:0170020"}


id: PBO:0043875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cAMP responsive element binding protein 3 like 3","termid":"PBO:0043875"}


id: PBO:0089103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"auxin family transmembrane transporter","termid":"PBO:0089103"}


id: GO:2000166
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of planar cell polarity pathway involved in pericardium morphogenesis.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of planar cell polarity pathway involved in pericardium morphogenesis (obsolete GO:2000166)","termid":"GO:2000166"}


id: MONDO:1010429
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atherosclerosis that occurs in Japanese quail.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"atherosclerosis, non-human animal","termid":"MONDO:1010008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atherosclerosis, Japanese quail","secondary_identifiers":["OMIA:000080-93934"],"termid":"MONDO:1010429","xrefs":{"Monarch":{"xref_id":"1010429"}}}


id: PBO:0036119
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_spindle_assembly_checkpoint","termid":"PBO:0036119"}


id: PBO:0057824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3143","termid":"PBO:0057824"}


id: MONDO:0013271
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"frontonasal dysplasia","termid":"MONDO:0016643"}],"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":"frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome","secondary_identifiers":["Orphanet:306542","DOID:0081047","MEDGEN:462056","OMIM:613456","UMLS:C3150706","GARD:12640"],"synonyms":[{"name":"ALX1-related frontonasal dysplasia","type":"exact"},{"name":"FND3","type":"related"},{"name":"frontonasal dysplasia 3","type":"related"},{"name":"frontonasal dysplasia type 3","type":"exact"}],"termid":"MONDO:0013271","xrefs":{"Monarch":{"xref_id":"0013271"}}}


id: PBO:0085235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pentafunctional arom protein; catalyzes steps 2 through 6 in the biosynthesis of chorismate, which is a precursor to aromatic amino acids","termid":"PBO:0085235"}


id: MONDO:0001592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolapse of female genital organ","secondary_identifiers":["UMLS:C0156349","ICD10CM:N81","ICD9:618.8","SCTID:73998008","MEDGEN:510253","ICD9:618.89","DOID:1284"],"termid":"MONDO:0001592","xrefs":{"Monarch":{"xref_id":"0001592"}}}


id: GO:0032148
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that initiates the activity of the inactive enzyme protein kinase B.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activation of protein kinase activity","termid":"GO:0032147"}],"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":"activation of protein kinase B activity","synonyms":[{"name":"protein kinase B activation","type":"exact"}],"termid":"GO:0032148"}


id: PBO:0113354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for production of 4-hydroxy-5-methylfuran-3(2H)-one (MHF); cupin superfamily protein; has structural resemblance to plant storage and ligand binding proteins (canavalin, glycinin, auxin binding protein) and to some enzymes (epimerase, germin); localizes to nucleus and cytoplasm","termid":"PBO:0113354"}


id: PBO:0046258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epididymal sperm binding protein 1","termid":"PBO:0046258"}


id: PBO:0071169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 8","termid":"PBO:0071169"}


id: PBO:0087216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-adenosylmethionine transporter of the mitochondrial inner membrane; member of the mitochondrial carrier family; required for biotin biosynthesis and respiratory growth","termid":"PBO:0087216"}


id: GO:0036209
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9beta-pimara-7,15-diene + 3 O2 + 3 reduced [NADPH-hemoprotein reductase] = 9beta-pimara-7,15-dien-19-oate + 4 H+ + 4 H2O + 3 oxidized [NADPH-hemoprotein reductase].","definition_xrefs":["RHEA:31951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"9beta-pimara-7,15-diene oxidase activity","secondary_identifiers":["GO:0102609","KEGG_REACTION:R09865","MetaCyc:RXN-15437","EC:1.14.14.111"],"synonyms":[{"name":"9-beta-stemod-13(17)-ene oxidase activity","type":"related"}],"termid":"GO:0036209"}


id: PBO:0078284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 17-1","termid":"PBO:0078284"}


id: PBO:0003688
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.7.4","termid":"PBO:0003688"}


id: PBO:0068772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 9","termid":"PBO:0068772"}


id: PBO:0061053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nipsnap homolog 1","termid":"PBO:0061053"}


id: GO:0050822
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in maintaining the structure and integrity of a peptide and preventing it from being degraded.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide metabolic process","termid":"GO:0006518"}],"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":"peptide stabilization","synonyms":[{"name":"peptide stabilisation","type":"exact"},{"name":"peptide stabilization activity","type":"related"}],"termid":"GO:0050822"}


id: GO:0062120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components during meiotic prophase to form a LinE complex, the protein complex that associates with chromatin to form linear elements in fission yeast. In S. pombe, the LinE complex contains four main structural components (Rec10, Rec25, Rec27, and Mug20) and other associated proteins.","definition_xrefs":["PMID:30640914"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"linear element assembly","termid":"GO:0030999"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0140013","GO:0044085","GO:0065003","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"LinE complex assembly","termid":"GO:0062120"}


id: FYPO:0005032
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 mutations occur at a normal (i.e. indistinguishable from wild type) frequency.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"},{"relation_name":"is_a","term_name":"vegetative cell phenotype","termid":"FYPO:0001320"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal mutation rate","synonyms":[{"name":"normal mutation rate during mitotic cell cycle","type":"related"},{"name":"normal mutation rate during vegetative growth","type":"exact"}],"termid":"FYPO:0005032"}


id: PBO:0064358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pro-melanin concentrating hormone like 1 (pseudogene)","termid":"PBO:0064358"}


id: FYPO:0003865
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell is lower than normal when the cell is in G0 phase. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level","termid":"FYPO:0000835"},{"relation_name":"is_a","term_name":"decreased level of substance in cell during G0","termid":"FYPO:0003864"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein level during G0","synonyms":[{"name":"decreased protein accumulation during G0","type":"related"},{"name":"decreased protein level during cell quiescence","type":"exact"},{"name":"decreased protein level during quiescence","type":"exact"},{"name":"reduced protein level during G0","type":"exact"}],"termid":"FYPO:0003865"}


id: MONDO:0035586
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cramp-fasciculation syndrome","secondary_identifiers":["MEDGEN:148299","UMLS:C0751381","Orphanet:581271","GARD:6205","ICD10CM:G90.8"],"termid":"MONDO:0035586","xrefs":{"Monarch":{"xref_id":"0035586"}}}


id: GO:0044012
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H2A L-lysine (position 9) = CoA + histone H2A N6-acetyl-L-lysine (position 9).","definition_xrefs":["PMID:18552846"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2A acetyltransferase activity","termid":"GO:0043998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016746","GO:0034212","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"histone H2AK9 acetyltransferase activity","synonyms":[{"name":"histone H2A-K9 acetyltransferase activity","type":"exact"},{"name":"histone acetylase activity (H2A-K9 specific)","type":"exact"},{"name":"histone acetyltransferase activity (H2A-K9 specific)","type":"exact"},{"name":"histone lysine N-acetyltransferase activity (H2A-K9 specific)","type":"exact"}],"termid":"GO:0044012"}


id: GO:0097141
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex consisting of BIM and BCL-2, members of the Bcl-2 family of anti- and proapoptotic regulators.","definition_xrefs":["GOC:so","PMID:14634621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bcl-2 family protein complex","termid":"GO:0097136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"BIM-BCL-2 complex","termid":"GO:0097141"}


id: GO:0045008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disruption of the bond between the sugar in the backbone and the C or T base, causing the base to be removed and leaving a depyrimidinated sugar.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"base-excision repair, AP site formation","termid":"GO:0006285"},{"relation_name":"is_a","term_name":"DNA modification","termid":"GO:0006304"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleotide catabolic process","termid":"GO:0009223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0044281","GO:0006259","GO:0008150","GO:0055086","GO:0006281"],"is_obsolete":false,"name":"depyrimidination","secondary_identifiers":["Reactome:R-HSA-73928"],"termid":"GO:0045008"}


id: PBO:0030282
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_sulfide:quinone_oxidoreductase_activity","termid":"PBO:0030282"}


id: FYPO:0002605
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 H2A phosphorylation occurs to a greater extent than normal at ribosomal DNA during G2 phase of the mitotic cell cycle. All histone H2A phosphorylation may be affected, or phosphorylation of specific sites on histone H2A may be increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H2A phosphorylation at rDNA during vegetative growth","termid":"FYPO:0002604"},{"relation_name":"is_a","term_name":"increased protein phosphorylation during mitotic G2 phase","termid":"FYPO:0004112"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0002494","FYPO:0002274"],"is_obsolete":false,"name":"increased histone H2A phosphorylation at rDNA during mitotic G2 phase","synonyms":[{"name":"increased histone H2A phosphorylation at rDNA during mitotic G2 phase during vegetative growth","type":"exact"},{"name":"increased histone H2A phosphorylation at ribosomal DNA during mitotic G2 phase","type":"exact"}],"termid":"FYPO:0002605"}


id: PBO:0051693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INO80B-WBP1 readthrough (NMD candidate)","termid":"PBO:0051693"}


id: GO:0102443
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD(1-) + a (2S)-2-hydroxycarboxylate = NADH(2-) + H+ + a 2-oxo carboxylate.","definition_xrefs":["GOC:pz","EC:1.1.1.337"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"L-2-hydroxycarboxylate dehydrogenase (NAD+) activity","secondary_identifiers":["RHEA:34555","MetaCyc:RXN-13927"],"termid":"GO:0102443"}


id: GO:1900484
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein targeting to vacuolar membrane.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein targeting to membrane","termid":"GO:0090315"},{"relation_name":"is_a","term_name":"negative regulation of intracellular protein transport","termid":"GO:0090317"},{"relation_name":"is_a","term_name":"regulation of protein targeting to vacuolar membrane","termid":"GO:1900483"},{"relation_name":"is_a","term_name":"negative regulation of vacuolar transport","termid":"GO:1903336"},{"relation_name":"negatively_regulates","term_name":"protein targeting to vacuolar membrane","termid":"GO:0044395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006605"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006605"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006605","GO:0006810"],"is_obsolete":false,"name":"negative regulation of protein targeting to vacuolar membrane","synonyms":[{"name":"down regulation of protein targeting to vacuolar membrane","type":"exact"},{"name":"down-regulation of protein targeting to vacuolar membrane","type":"exact"},{"name":"downregulation of protein targeting to vacuolar membrane","type":"exact"},{"name":"inhibition of protein targeting to vacuolar membrane","type":"narrow"}],"termid":"GO:1900484"}


id: PBO:0085594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in bud-site selection; diploid mutants display a random budding pattern instead of the wild-type bipolar pattern","termid":"PBO:0085594"}


id: PBO:0057179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 330","termid":"PBO:0057179"}


id: GO:0047488
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the eliminative cleavage of polysaccharides containing 1,4-linked D-glucuronate or L-iduronate residues and 1,4-alpha-linked 2-sulfoamino-2-deoxy-6-sulfo-D-glucose residues to give oligosaccharides with terminal 4-deoxy-alpha-D-gluc-4-enuronosyl groups at their nonreducing ends.","definition_xrefs":["MetaCyc:4.2.2.7-RXN","EC:4.2.2.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on polysaccharides","termid":"GO:0016837"}],"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:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"heparin lyase activity","synonyms":[{"name":"heparan sulfate lyase activity","type":"related"},{"name":"heparin eliminase activity","type":"related"},{"name":"heparinase activity","type":"related"}],"termid":"GO:0047488"}


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


id: PBO:0028782
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_transposable_element-derived_small_RNA_level","termid":"PBO:0028782"}


id: PBO:0011110
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spt6 binding correlates with that of RNAPII at the heterochromatin","termid":"PBO:0011110"}


id: PBO:0017939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cactin, spliceosome complex subunit","termid":"PBO:0017939"}


id: MONDO:0035838
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Castleman disease","termid":"MONDO:0015564"}],"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":"idiopathic multicentric Castleman disease","secondary_identifiers":["GARD:22309","MEDGEN:1680858","UMLS:C5197665","Orphanet:570431"],"synonyms":[{"name":"HHV-8-negative multicentric Castleman disease","type":"exact"},{"name":"Human herpesvirus-8-negative multicentric Castleman disease","type":"exact"}],"termid":"MONDO:0035838","xrefs":{"Monarch":{"xref_id":"0035838"}}}


id: PBO:0051725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INSYN1 antisense RNA 1","termid":"PBO:0051725"}


id: PBO:0008425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic protein, implicated in vesicle-mediated transport","termid":"PBO:0008425"}


id: MONDO:0007123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyloblepharon filiforme adnatum-cleft palate syndrome","secondary_identifiers":["UMLS:C1862866","SCTID:400952003","MEDGEN:400148","GARD:696","MESH:C536373","OMIM:106250","Orphanet:1072"],"synonyms":[{"name":"AFA","type":"related"},{"name":"ankyloblepharon filiforme adnatum","type":"exact"},{"name":"ankyloblepharon filiforme adnatum and cleft palate","type":"related"},{"name":"ankyloblepharon filiforme adnatum cleft palate","type":"related"},{"name":"ankyloblepharon filiforme congenitum","type":"related"},{"name":"congenital filiform fusion of the eyelids with cleft palate and/or cleft lip","type":"related"}],"termid":"MONDO:0007123","xrefs":{"Monarch":{"xref_id":"0007123"}}}


id: PBO:0047820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box O1","termid":"PBO:0047820"}


id: PBO:0082367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAR domain protein that localizes to early and late Golgi vesicles; required for adaptation to varying nutrient concentrations, fluid-phase endocytosis, polarization of the actin cytoskeleton, and vacuole biogenesis","termid":"PBO:0082367"}


id: GO:0038122
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the C-C motif chemokine 5 (CCL5) and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-C chemokine receptor activity","termid":"GO:0016493"}],"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":"C-C motif chemokine 5 receptor activity","synonyms":[{"name":"CCL5 receptor activity","type":"exact"},{"name":"RANTES receptor activity","type":"exact"},{"name":"small inducible cytokine A5 receptor activity","type":"exact"}],"termid":"GO:0038122"}


id: PBO:0074085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 26 member 2","termid":"PBO:0074085"}


id: FYPO:0009096
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is increased relative to normal in a medium containing xylose as the carbon source.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000003","FYPO:0002058","FYPO:0001985","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"increased cell population growth on xylose carbon source","synonyms":[{"name":"increased growth on xylose carbon source","type":"broad"},{"name":"increased vegetative cell growth on xylose carbon source","type":"exact"}],"termid":"FYPO:0009096"}


id: GO:0009798
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment, maintenance and elaboration of a pattern along a line or around a point.","definition_xrefs":["GOC:isa_complete","GOC:go_curators","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification process","termid":"GO:0007389"}],"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":"axis specification","synonyms":[{"name":"axis determination","type":"related"}],"termid":"GO:0009798"}


id: GO:0021536
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the diencephalon over time, from its formation to the mature structure. The diencephalon is the paired caudal parts of the prosencephalon from which the thalamus, hypothalamus, epithalamus and subthalamus are derived; these regions regulate autonomic, visceral and endocrine function, and process information directed to the cerebral cortex.","definition_xrefs":["GOC:cls","GOC:dph","ISBN:0838580343","GOC:jid","GOC:dgh","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"forebrain development","termid":"GO:0030900"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"diencephalon development","termid":"GO:0021536"}


id: GO:0042571
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An immunoglobulin complex that is secreted into extracellular space and found in mucosal areas or other tissues or circulating in the blood or lymph. In its canonical form, a circulating immunoglobulin complex is composed of two identical heavy chains and two identical light chains, held together by disulfide bonds. Some forms of are polymers of the basic structure and contain additional components such as J-chain and the secretory component.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin complex","termid":"GO:0019814"},{"relation_name":"part_of","term_name":"extracellular space","termid":"GO:0005615"}],"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:0032991","GO:0005575","GO:0005576"],"is_obsolete":false,"name":"immunoglobulin complex, circulating","secondary_identifiers":["Wikipedia:Antibody"],"synonyms":[{"name":"antibody","type":"exact"}],"termid":"GO:0042571"}


id: PBO:0072469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 33","termid":"PBO:0072469"}


id: MONDO:0009999
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive Robinow syndrome (RRS) is the less common type of Robinow syndrome (RS) characterized by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.","definition_xrefs":["Orphanet:1507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Robinow syndrome","termid":"MONDO:0019978"}],"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":"autosomal recessive Robinow syndrome","secondary_identifiers":["UMLS:C5399974","DOID:0060764","GARD:16568","MEDGEN:1770070","MESH:C535863","OMIM:268310","icd11.foundation:793292660"],"synonyms":[{"name":"COVESDEM syndrome","type":"exact"},{"name":"Covesdem syndrome","type":"related"},{"name":"Covesdem syndrome, formerly","type":"related"},{"name":"RRS","type":"exact"},{"name":"Robinow syndrome, autosomal recessive","type":"exact"},{"name":"Robinow syndrome, autosomal recessive, with Brachy-syn-polydactyly","type":"related"},{"name":"Robinow syndrome, autosomal recessive, with aplasia/hypoplasia of phalanges and metacarpals/metatarsals","type":"related"},{"name":"costovertebral segmentation defect with mesomelia","type":"related"},{"name":"costovertebral segmentation defect with mesomelia, formerly","type":"related"},{"name":"costovertebral segmentation defect-mesomelia syndrome","type":"exact"}],"termid":"MONDO:0009999","xrefs":{"Monarch":{"xref_id":"0009999"}}}


id: PBO:0005720
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"renal cell cancer","termid":"PBO:0005720"}


id: PBO:0051064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 4-11 (non-functional)","termid":"PBO:0051064"}


id: PR:O13908
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC22A12.17c gene.","definition_xrefs":["UniProtKB:O13908","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 oxidoreductase C22A12.17c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22A12.17c","synonyms":[{"name":"Spom972h-SPAC22A12.17c","type":"exact"}],"termid":"PR:O13908"}


id: MONDO:1040050
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any ciliopathy caused by variants in the MKKS gene.","definition_xrefs":["PMID:22446187","PMID:20472660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliopathy","termid":"MONDO:0005308"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MKKS-related ciliopathy","synonyms":[{"name":"MKKS-related ciliopathy","type":"exact"}],"termid":"MONDO:1040050","xrefs":{"Monarch":{"xref_id":"1040050"}}}


id: MONDO:0032739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 36","secondary_identifiers":["DOID:0111921","MEDGEN:1678385","OMIM:618420","UMLS:C5193086"],"synonyms":[{"name":"SPERMATOGENIC FAILURE 36","type":"related"},{"name":"SPGF36","type":"related"}],"termid":"MONDO:0032739","xrefs":{"Monarch":{"xref_id":"0032739"}}}


id: PBO:0052920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 19-3","termid":"PBO:0052920"}


id: MOD:01344
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical with MOD:00835. Remap to MOD:00835.","definition_xrefs":["PubMed:9252331","Unimod:401","PubMed:9276974"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01344 dehydrogenated residue - site S (obsolete MOD:01344)","synonyms":[{"name":"2-amino-3-oxo-butanoic_acid","type":"related"},{"name":"Didehydro","type":"related"}],"termid":"MOD:01344"}


id: PBO:0084855
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; not essential for mitochondrial translation","termid":"PBO:0084855"}


id: PBO:0034092
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-results_in_catabolism_of","termid":"PBO:0034092"}


id: GO:0052573
data:
  {"annotated_genes":["SJAG_01784","SJAG_03818","SJAG_02950","SJAG_02954","SJAG_02951"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113171,113153,109053,113160,113161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052574"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving UDP-D-galactose, a substance composed of D-galactose in glycosidic linkage with guanosine diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar metabolic process","termid":"GO:0009225"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01784":null,"SJAG_02950":null,"SJAG_02951":null,"SJAG_02954":null,"SJAG_03818":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"UDP-D-galactose metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"UDP-D-galactopyranose metabolic process","type":"exact"},{"name":"UDP-D-galactopyranose metabolism","type":"exact"},{"name":"UDP-D-galactose metabolism","type":"exact"},{"name":"UDP-galactose metabolic process","type":"exact"},{"name":"UDP-galactose metabolism","type":"exact"},{"name":"uridine diphosphate galactose metabolic process","type":"exact"},{"name":"uridine diphosphate galactose metabolism","type":"exact"}],"termid":"GO:0052573","terms_by_termid":{"GO:0052574":null}}


id: PBO:0028140
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_18S_rRNA_level","termid":"PBO:0028140"}


id: GO:0047453
data:
  {"annotated_genes":["SJAG_03669"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[117060],"is_not":false,"summary":null,"term":"GO:0047453"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (6S)-6beta-hydroxy-1,4,5,6-tetrahydronicotinamide adenine dinucleotide + ATP = ADP + H+ + NAD(P)H + phosphate.","definition_xrefs":["PMID:3061454","EC:4.2.1.93"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03669":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"ATP-dependent NAD(P)H-hydrate dehydratase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R00129","MetaCyc:4.2.1.93-RXN","Reactome:R-HSA-6806967"],"synonyms":[{"name":"(6S)-beta-6-hydroxy-1,4,5,6-tetrahydronicotinamide-adenine-dinucleotide hydro-lyase (ATP-hydrolysing)","type":"related"},{"name":"(6S)-beta-6-hydroxy-1,4,5,6-tetrahydronicotinamide-adenine-dinucleotide hydro-lyase(ATP-hydrolysing; NADH-forming)","type":"related"},{"name":"ATP-dependent H(4)NAD(P)OH dehydratase activity","type":"exact"},{"name":"ATP-dependent H4NAD(P)OH dehydratase activity","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide hydrate dehydratase activity","type":"broad"}],"termid":"GO:0047453","terms_by_termid":{"GO:0047453":null}}


id: PBO:0069054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 300, pseudogene","termid":"PBO:0069054"}


id: PBO:0054444
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 1841","termid":"PBO:0054444"}


id: MONDO:0007291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete familial cerebral cavernous malformation (obsolete MONDO:0007291)","termid":"MONDO:0007291","xrefs":{"Monarch":{"xref_id":"0007291"}}}


id: PBO:0063331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 7","termid":"PBO:0063331"}


id: FYPO:0003371
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the actomyosin contractile ring is abolished, and the protein is present in the cytoplasm instead.","definition_xrefs":["PMID:18256290","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to actomyosin contractile ring","termid":"FYPO:0002561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0000631","FYPO:0001985","FYPO:0000032","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein localization to actomyosin contractile ring, with protein mislocalized to cytoplasm","synonyms":[{"name":"abolished protein localisation to actomyosin contractile ring, with protein mislocalized to cytoplasm","type":"exact"},{"name":"abolished protein localization to actomyosin contractile ring, with protein mislocalized to cytoplasm during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to actomyosin contractile ring, with protein mislocalized to cytoplasm, during vegetative growth","type":"exact"},{"name":"abolished protein localization to contractile ring, with protein mislocalized to cytoplasm","type":"exact"},{"name":"abolished protein localization to cytokinetic contractile ring, with protein mislocalized to cytoplasm","type":"exact"},{"name":"abolished protein localization to mitotic contractile ring, with protein mislocalized to cytoplasm","type":"exact"},{"name":"abolished protein recruitment to actomyosin contractile ring, with protein mislocalized to cytoplasm","type":"related"},{"name":"protein localization to actomyosin contractile ring abolished, with protein mislocalized to cytoplasm","type":"exact"}],"termid":"FYPO:0003371"}


id: PBO:0090722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoplasmic glutaminyl-tRNA ligase Qrs1","termid":"PBO:0090722"}


id: GO:0030729
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetoacetate + ATP + CoA = acetoacetyl-CoA + AMP + diphosphate + H+.","definition_xrefs":["EC:6.2.1.16","RHEA:16117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-ligase activity","termid":"GO:0016405"},{"relation_name":"is_a","term_name":"acid-thiol ligase activity","termid":"GO:0016878"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"acetoacetate-CoA ligase activity","secondary_identifiers":["MetaCyc:ACETOACETATE--COA-LIGASE-RXN","Reactome:R-HSA-5694494","KEGG_REACTION:R01357"],"synonyms":[{"name":"acetoacetate:CoA ligase (AMP-forming)","type":"related"},{"name":"acetoacetyl-CoA synthetase activity","type":"exact"}],"termid":"GO:0030729"}


id: PBO:0002194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1761 family protein","termid":"PBO:0002194"}


id: PBO:0072077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S12 pseudogene 7","termid":"PBO:0072077"}


id: PBO:0073452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SFT2 domain containing 1","termid":"PBO:0073452"}


id: MONDO:0020717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"isolated familial wooly hair disorder","termid":"MONDO:0008686"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal dominant wooly hair","secondary_identifiers":["UMLS:C1860238","OMIM:194300","DOID:0111573","MEDGEN:348571"],"synonyms":[{"name":"ADWH","type":"related"},{"name":"woolly hair, autosomal dominant","type":"exact"},{"name":"wooly hair, autosomal dominant","type":"exact"}],"termid":"MONDO:0020717","xrefs":{"Monarch":{"xref_id":"0020717"}}}


id: GO:0072232
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the S2 portion of the metanephric proximal convoluted tubule over time, from its formation to the mature structure. The S2 portion of the metanephric proximal tubule is involved in reabsorption of water and sodium chloride.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proximal convoluted tubule segment 2 development","termid":"GO:0072032"},{"relation_name":"part_of","term_name":"metanephric proximal convoluted tubule development","termid":"GO:0072229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric proximal convoluted tubule segment 2 development","synonyms":[{"name":"metanephric S2 development","type":"exact"}],"termid":"GO:0072232"}


id: PBO:0047917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, BrdU type, rare, fra(10)(q25.2)","termid":"PBO:0047917"}


id: PBO:0083103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA helicase encoded within the telomeric Y' element; Y' -helicase protein 1","termid":"PBO:0083103"}


id: PBO:0042505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 24","termid":"PBO:0042505"}


id: PBO:0043133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 1","termid":"PBO:0043133"}


id: PBO:0045939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ephrin A4","termid":"PBO:0045939"}


id: PBO:0075804
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 3, pseudogene","termid":"PBO:0075804"}


id: GO:0018729
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + propanoate = acetate + propanoyl-CoA.","definition_xrefs":["EC:2.8.3.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-transferase activity","termid":"GO:0008410"}],"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:0016782"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016782","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"propionate CoA-transferase activity","secondary_identifiers":["UM-BBD_reactionID:r0087","MetaCyc:PROPIONATE-COA-TRANSFERASE-RXN","RHEA:23520"],"synonyms":[{"name":"acetyl-CoA:propanoate CoA-transferase activity","type":"related"},{"name":"propionate coenzyme A-transferase activity","type":"related"},{"name":"propionate-CoA:lactoyl-CoA transferase activity","type":"related"},{"name":"propionyl CoA:acetate CoA transferase activity","type":"related"},{"name":"propionyl-CoA transferase activity","type":"related"}],"termid":"GO:0018729"}


id: PBO:0062166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily K member 7 pseudogene","termid":"PBO:0062166"}


id: PBO:0069482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 749, pseudogene","termid":"PBO:0069482"}


id: PBO:0061013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nidogen 1","termid":"PBO:0061013"}


id: PBO:0073022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterol carrier protein 2","termid":"PBO:0073022"}


id: MONDO:0013120
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46,XY complete gonadal dysgenesis","termid":"MONDO:0010765"}],"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":"46,XY sex reversal 5","secondary_identifiers":["MESH:C567766","GARD:15611","MEDGEN:414349","UMLS:C2751317","OMIM:613080","DOID:0111776"],"synonyms":[{"name":"46,XY SEX reversal 5","type":"related"},{"name":"46,XY Sex reversal type 5","type":"exact"},{"name":"46,XY Sex reversal, Cbx2-related","type":"related"},{"name":"46,XY gonadal dysgenesis, complete, Cbx2-related","type":"related"},{"name":"46,XY sex reversal 5","type":"exact"},{"name":"46XY sex reversal 5","type":"exact"},{"name":"SRXY5","type":"related"},{"name":"Sex reversal, XY, Cbx2-related","type":"related"},{"name":"disorder of Sex development, 46,XY, Cbx2-related","type":"related"}],"termid":"MONDO:0013120","xrefs":{"Monarch":{"xref_id":"0013120"}}}


id: PBO:0090338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABC transmembrane transporter Abc1/Ybt1","termid":"PBO:0090338"}


id: MONDO:0005015
data:
  {"annotated_genes":["SJAG_00092","SJAG_04334","SJAG_02000","SJAG_02426","SJAG_02013","SJAG_03247","SJAG_00214","SJAG_04495","SJAG_02012","SJAG_04206","SJAG_04394"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86871,86870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014488"},{"annotations":[86794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014674"},{"annotations":[84670,84671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007453"},{"annotations":[85942,85941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100165"},{"annotations":[84666,86796,86798,86797,84669,84665,84668,84667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0005148"}]},"cv_name":"mondo","definition":"A metabolic disorder characterized by abnormally high blood sugar levels due to diminished production of insulin or insulin resistance/desensitization.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine pancreas disorder","termid":"MONDO:0001933"},{"relation_name":"is_a","term_name":"glucose metabolism disease","termid":"MONDO:0002908"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00092":null,"SJAG_00214":null,"SJAG_02000":null,"SJAG_02012":null,"SJAG_02013":null,"SJAG_02426":null,"SJAG_03247":null,"SJAG_04206":null,"SJAG_04334":null,"SJAG_04394":null,"SJAG_04495":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"diabetes mellitus","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2100157","SCTID:73211009","ICD10CM:E08-E13","NCIT:C2985","UMLS:C0011849","icd11.foundation:465177735","DOID:9351","EFO:0000400","HP:0000819","MEDGEN:8350","MESH:D003920","NANDO:2100158","ICD9:250"],"synonyms":[{"name":"DM","type":"exact"},{"name":"diabetes","type":"exact"},{"name":"diabetes mellitus","type":"exact"},{"name":"diabetes mellitus (disease)","type":"exact"}],"termid":"MONDO:0005015","terms_by_termid":{"MONDO:0005148":null,"MONDO:0007453":null,"MONDO:0014488":null,"MONDO:0014674":null,"MONDO:0100165":null},"xrefs":{"Monarch":{"xref_id":"0005015"}}}


id: MONDO:0017866
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital pulmonary valve stenosis","termid":"MONDO:0017865"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subpulmonary stenosis","secondary_identifiers":["icd11.foundation:1393194578","GARD:5051","SCTID:448476001","MEDGEN:757434","Orphanet:3190","UMLS:C3165028"],"termid":"MONDO:0017866","xrefs":{"Monarch":{"xref_id":"0017866"}}}


id: PR:O60150
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- any1 gene.","definition_xrefs":["UniProtKB:O60150","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C18H10.20c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18H10.20c","synonyms":[{"name":"Spom972h-any1","type":"exact"}],"termid":"PR:O60150"}


id: MONDO:1010694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AL amyloidosis that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AL amyloidosis, non-human animal","termid":"MONDO:1010093"},{"relation_name":"is_a","term_name":"hypertrophic cardiomyopathy, domestic cat","termid":"MONDO:1010459"},{"relation_name":"is_a","term_name":"amyloidosis, domestic cat","termid":"MONDO:1011468"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AL amyloidosis, domestic cat","secondary_identifiers":["OMIA:000039-9685"],"termid":"MONDO:1010694","xrefs":{"Monarch":{"xref_id":"1010694"}}}


id: GO:1902608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of large conductance calcium-activated potassium channel activity.","definition_xrefs":["GO_REF:0000059","PMID:23407708","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of potassium ion transmembrane transporter activity","termid":"GO:1901018"},{"relation_name":"is_a","term_name":"positive regulation of cation channel activity","termid":"GO:2001259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of large conductance calcium-activated potassium channel activity","synonyms":[{"name":"activation of BK KCa channels","type":"narrow"},{"name":"activation of BK calcium-activated potassium channel activity","type":"narrow"},{"name":"activation of BK channel activity","type":"related"},{"name":"activation of large conductance KCa channels","type":"narrow"},{"name":"activation of large conductance calcium-activated potassium channel activity","type":"narrow"},{"name":"positive regulation of BK KCa channels","type":"exact"},{"name":"positive regulation of BK calcium-activated potassium channel activity","type":"exact"},{"name":"positive regulation of BK channel activity","type":"related"},{"name":"positive regulation of large conductance KCa channels","type":"exact"},{"name":"up regulation of BK KCa channels","type":"exact"},{"name":"up regulation of BK calcium-activated potassium channel activity","type":"exact"},{"name":"up regulation of BK channel activity","type":"related"},{"name":"up regulation of large conductance KCa channels","type":"exact"},{"name":"up regulation of large conductance calcium-activated potassium channel activity","type":"exact"},{"name":"up-regulation of BK KCa channels","type":"exact"},{"name":"up-regulation of BK calcium-activated potassium channel activity","type":"exact"},{"name":"up-regulation of BK channel activity","type":"related"},{"name":"up-regulation of large conductance KCa channels","type":"exact"},{"name":"up-regulation of large conductance calcium-activated potassium channel activity","type":"exact"},{"name":"upregulation of BK KCa channels","type":"exact"},{"name":"upregulation of BK calcium-activated potassium channel activity","type":"exact"},{"name":"upregulation of BK channel activity","type":"related"},{"name":"upregulation of large conductance KCa channels","type":"exact"},{"name":"upregulation of large conductance calcium-activated potassium channel activity","type":"exact"}],"termid":"GO:1902608"}


id: PBO:0057680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1269b","termid":"PBO:0057680"}


id: PR:Q9UTL7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GPN-loop GTPase 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01930","PANTHER:PTHR21231:SF3","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":"GPN-loop GTPase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC144.07c","secondary_identifiers":["UniProtKB:Q9UTL7"],"synonyms":[{"name":"ATP-binding domain 1 family member B homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-GPN2","type":"exact"}],"termid":"PR:Q9UTL7"}


id: PBO:0029344
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitochondrial_tRNA_absent_from_cell","termid":"PBO:0029344"}


id: PBO:0083351
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps the verified gene HIP1/YGR191W","termid":"PBO:0083351"}


id: PBO:0058657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6785","termid":"PBO:0058657"}


id: SO:1001264
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A recoded_mRNA where translation was suspended at a particular codon and resumed at a particular non-overlapping downstream codon.","direct_ancestors":[{"relation_name":"has_quality","term_name":"recoded_by_translational_bypass","termid":"SO:0000886"},{"relation_name":"is_a","term_name":"recoded_mRNA","termid":"SO:1001261"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA_recoded_by_translational_bypass","synonyms":[{"name":"mRNA recoded by translational bypass","type":"exact"}],"termid":"SO:1001264"}


id: GO:0018267
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a C-terminal peptidyl-cysteine ethanolamide-linked glycosylphosphatidylinositol (GPI) anchor following hydrolysis of a cysteinyl-peptide bond in the carboxy-terminal region of a membrane-associated protein.","definition_xrefs":["RESID:AA0160"],"gene_count":0,"genotype_count":0,"name":"obsolete GPI anchor biosynthetic process via N-cysteinyl-glycosylphosphatidylinositolethanolamine (obsolete GO:0018267)","termid":"GO:0018267"}


id: PBO:0083911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Folylpolyglutamate synthetase; catalyzes extension of the glutamate chains of the folate coenzymes, required for methionine synthesis and for maintenance of mitochondrial DNA; protein abundance increases in response to DNA replication stress","termid":"PBO:0083911"}


id: GO:0022619
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a generative cell. The generative cell gives rise to the sperm cells in the male gametophyte.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"microgametogenesis","termid":"GO:0055046"}],"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":"generative cell differentiation","termid":"GO:0022619"}


id: GO:0021938
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of activation of the transmembrane protein Smoothened in cerebellar granule cells that contributes to the regulation of proliferation of the cells.","definition_xrefs":["GOC:dph","GOC:jid","GOC:dgh","GOC:tb","GO_REF:0000021","PMID:15157725","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smoothened signaling pathway","termid":"GO:0007224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"smoothened signaling pathway involved in regulation of cerebellar granule cell precursor cell proliferation","synonyms":[{"name":"hedgehog signaling pathway involved in regulation of granule cell precursor cell proliferation","type":"exact"},{"name":"hh signaling pathway involved in regulation of granule cell precursor cell proliferation","type":"exact"},{"name":"smoothened signalling pathway in regulation of granule cell precursor cell proliferation","type":"exact"}],"termid":"GO:0021938"}


id: PBO:0063796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHD finger protein 24","termid":"PBO:0063796"}


id: GO:0141000
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a ubiquitin molecule to histone 4 at the lysine-91 residue.","definition_xrefs":["PMID:19818714"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H4 ubiquitin ligase activity","termid":"GO:0141056"}],"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:0004842"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0019787"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016740","GO:0016746","GO:0004842","GO:0140096","GO:0003674","GO:0003824","GO:0019787"],"is_obsolete":false,"name":"histone H4K91 ubiquitin ligase activity","synonyms":[{"name":"histone H4-K91 ubiquitin ligase activity","type":"exact"},{"name":"histone ubiquitin ligase activity (H4-K91 specific)","type":"exact"}],"termid":"GO:0141000"}


id: PBO:0060811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit V3","termid":"PBO:0060811"}


id: PATO:0000077
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the whether the bearer's disposition to react to a stimulus or an agent.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"response to","synonyms":[{"name":"responsivity","type":"related"}],"termid":"PATO:0000077"}


id: MONDO:0013460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SP7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"osteogenesis imperfecta type 12","secondary_identifiers":["GARD:15722","DOID:0110348","MEDGEN:462783","OMIM:613849","UMLS:C3151433"],"synonyms":[{"name":"OI, type 12","type":"related"},{"name":"OI12","type":"exact"},{"name":"SP7 osteogenesis imperfecta","type":"exact"},{"name":"osteogenesis imperfecta caused by mutation in SP7","type":"exact"},{"name":"osteogenesis imperfecta type XII","type":"exact"},{"name":"osteogenesis imperfecta, type 12","type":"related"},{"name":"osteogenesis imperfecta, type XII","type":"related"}],"termid":"MONDO:0013460","xrefs":{"Monarch":{"xref_id":"0013460"}}}


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


id: internal:reserved_name
data:
  {"annotation_feature_type":"gene","cv_name":"synonym_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reserved_name","termid":"internal:reserved_name"}


id: PBO:0073336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family A member 12","termid":"PBO:0073336"}


id: PBO:0046780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EYA transcriptional coactivator and phosphatase 1","termid":"PBO:0046780"}


id: PBO:0001529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GDP dissociation inhibitor Gdi1 (predicted)","termid":"PBO:0001529"}


id: GO:0033966
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-benzylformamide + H2O = formate + benzylamine.","definition_xrefs":["EC:3.5.1.91"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824","GO:0016810"],"is_obsolete":false,"name":"N-substituted formamide deformylase activity","secondary_identifiers":["MetaCyc:3.5.1.91-RXN","RHEA:12096"],"synonyms":[{"name":"N-benzylformamide amidohydrolase activity","type":"related"},{"name":"NfdA","type":"related"}],"termid":"GO:0033966"}


id: GO:0015127
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of bilirubin from one side of a membrane to the other. Bilirubin is a linear tetrapyrrole produced in the reticuloendothelial system from biliverdin and transported to the liver as a complex with serum albumin. In the liver, bilirubin is converted to bilirubin bisglucuronide, which is excreted in the bile.","definition_xrefs":["GOC:ai","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transmembrane transporter activity","termid":"GO:0005310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"bilirubin transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-9661417","Reactome:R-HSA-5679031","Reactome:R-HSA-5679041"],"termid":"GO:0015127"}


id: GO:0072077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the renal vesicle are generated and organized. The renal vesicle is the primordial structure of the nephron epithelium, and is formed by the condensation of mesenchymal cells.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"},{"relation_name":"part_of","term_name":"renal vesicle development","termid":"GO:0072087"},{"relation_name":"part_of","term_name":"nephron epithelium morphogenesis","termid":"GO:0072088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal vesicle morphogenesis","termid":"GO:0072077"}


id: PR:O59804
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 10 kDa chaperonin that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04591"],"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":"10 kDa heat shock protein, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC550.06c","secondary_identifiers":["UniProtKB:O59804"],"synonyms":[{"name":"10 kDa chaperonin (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"HSP10 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-groS","type":"exact"}],"termid":"PR:O59804"}


id: PBO:0091375
data:
  {"annotation_feature_type":"gene","cv_name":"external_link","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"the electron microscopy databank","termid":"PBO:0091375"}


id: PBO:0053601
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 630","termid":"PBO:0053601"}


id: GO:0003271
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of activation of the transmembrane protein Smoothened contributing to the modulation of the frequency, rate or extent of cardioblast proliferation in the secondary heart field. A cardioblast is a cardiac precursor cell. It is a cell that has been committed to a cardiac fate, but will undergo more cell division rather than terminally differentiating.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smoothened signaling pathway","termid":"GO:0007224"},{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway involved in heart development","termid":"GO:0061311"},{"relation_name":"part_of","term_name":"regulation of secondary heart field cardioblast proliferation","termid":"GO:0003266"}],"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":"smoothened signaling pathway involved in regulation of secondary heart field cardioblast proliferation","synonyms":[{"name":"hedgehog signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"hh signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signaling pathway involved in regulation of secondary heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signalling pathway involved in regulation of secondary heart field cardioblast proliferation","type":"exact"}],"termid":"GO:0003271"}


id: GO:0044543
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process which begins with venom being forced into an organism by the bite or sting of another organism, and ends with the proteolytic processing of an inactive enzyme to an active form.","definition_xrefs":["GOC:fj","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete envenomation resulting in zymogen activation in another organism (obsolete GO:0044543)","synonyms":[{"name":"envenomation resulting in zymogen activation in other organism","type":"exact"}],"termid":"GO:0044543"}


id: PBO:0070611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 79","termid":"PBO:0070611"}


id: GO:1902433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of water channel activity that is involved in maintenance of lens transparency.","definition_xrefs":["PMID:22095752","GOC:nhn","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of water channel activity involved in maintenance of lens transparency (obsolete GO:1902433)","synonyms":[{"name":"activation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"activation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"activation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"activation of water channel activity involved in maintenance of lens transparency","type":"narrow"},{"name":"activation of water channel activity involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"activation of water channel activity involved in preservation of lens transparency","type":"narrow"},{"name":"aquaporin activation involved in maintenance of lens transparency","type":"narrow"},{"name":"aquaporin activation involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"aquaporin activation involved in preservation of lens transparency","type":"narrow"},{"name":"positive regulation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"positive regulation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"positive regulation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"positive regulation of water channel activity involved in maintenance of ocular lens transparency","type":"exact"},{"name":"positive regulation of water channel activity involved in preservation of lens transparency","type":"exact"},{"name":"up regulation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"up regulation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"up regulation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"up regulation of water channel activity involved in maintenance of lens transparency","type":"exact"},{"name":"up regulation of water channel activity involved in maintenance of ocular lens transparency","type":"exact"},{"name":"up regulation of water channel activity involved in preservation of lens transparency","type":"exact"},{"name":"up-regulation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"up-regulation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"up-regulation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"up-regulation of water channel activity involved in maintenance of lens transparency","type":"exact"},{"name":"up-regulation of water channel activity involved in maintenance of ocular lens transparency","type":"exact"},{"name":"up-regulation of water channel activity involved in preservation of lens transparency","type":"exact"},{"name":"upregulation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"upregulation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"upregulation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"upregulation of water channel activity involved in maintenance of lens transparency","type":"exact"},{"name":"upregulation of water channel activity involved in maintenance of ocular lens transparency","type":"exact"},{"name":"upregulation of water channel activity involved in preservation of lens transparency","type":"exact"}],"termid":"GO:1902433"}


id: GO:0045020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. DNA repair pathways that tend to increase the endogenous mutation rate.","definition_xrefs":["GOC:jl","PMID:11459974"],"gene_count":0,"genotype_count":0,"name":"obsolete error-prone DNA repair (obsolete GO:0045020)","synonyms":[{"name":"error-prone DNA repair","type":"exact"},{"name":"mutagenic DNA repair","type":"exact"}],"termid":"GO:0045020"}


id: MONDO:0004236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A somatostatin-producing neuroendocrine tumor that arises from the duodenum. It is characterized by the presence of tubulo-glandular structures.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"duodenum cancer","termid":"MONDO:0000920"},{"relation_name":"is_a","term_name":"duodenal neuroendocrine tumor, well differentiated, low or intermediate grade","termid":"MONDO:0015063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"duodenal somatostatinoma","secondary_identifiers":["NCIT:C27407","UMLS:C1333320","MEDGEN:234205","DOID:7479"],"synonyms":[{"name":"duodenal delta cell somatostatin producing tumor","type":"exact"},{"name":"duodenal delta cell somatostatin producing tumour","type":"exact"},{"name":"duodenal somatostatin producing tumor","type":"exact"},{"name":"duodenal somatostatin producing tumour","type":"exact"},{"name":"duodenal somatostatin-producing NET","type":"exact"},{"name":"duodenal somatostatin-producing neuroendocrine tumor","type":"exact"},{"name":"duodenal somatostatin-producing neuroendocrine tumour","type":"exact"},{"name":"duodenal somatostatinoma","type":"exact"}],"termid":"MONDO:0004236","xrefs":{"Monarch":{"xref_id":"0004236"}}}


id: MONDO:0018547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute tricyclic antidepressant (TCA) poisoning is a potentially lethal intoxication that is characterized by life-threatening arrhythmias (sinus tachycardias, premature ventricular contractions, ventricular arrhythmias), anticholinergic toxidrome (mydriasis, dry mucous membrane, tachycardia, hypertension), central nervous system toxicity (lethargy, coma, myoclonic jerks), refractory hypotension, and sudden death.","definition_xrefs":["Orphanet:43117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute tricyclic antidepressant poisoning","secondary_identifiers":["UMLS:C5681319","MEDGEN:1830115"],"termid":"MONDO:0018547","xrefs":{"Monarch":{"xref_id":"0018547"}}}


id: PBO:0039735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein D","termid":"PBO:0039735"}


id: PBO:0068998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 242, pseudogene","termid":"PBO:0068998"}


id: MONDO:0017269
data:
  {"annotated_genes":["SJAG_02855"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"}]},"cv_name":"mondo","definition":"X-linked form of inherited ichthyosis syndromic form.","definition_xrefs":["MONDO:patterns/x_linked"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02855":null},"genotype_count":0,"is_obsolete":false,"name":"X-linked ichthyosis syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:281210","GARD:21109","MedDRA:10048063"],"synonyms":[{"name":"X-linked inherited ichthyosis syndromic form","type":"exact"},{"name":"inherited ichthyosis syndromic form, X-linked","type":"exact"}],"termid":"MONDO:0017269","terms_by_termid":{"MONDO:0010621":null},"xrefs":{"Monarch":{"xref_id":"0017269"}}}


id: MONDO:0007210
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":"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay","secondary_identifiers":["UMLS:C1862171","MEDGEN:396307","MESH:C566206","OMIM:112370"],"synonyms":[{"name":"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay","type":"exact"}],"termid":"MONDO:0007210","xrefs":{"Monarch":{"xref_id":"0007210"}}}


id: PBO:0045319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double C2 domain beta","termid":"PBO:0045319"}


id: PBO:0073810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC6A14 pseudogene 1","termid":"PBO:0073810"}


id: MONDO:0000240
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aspergillosis that is a serious fungal infection of the lung with pneumonia caused by Aspergillus, which spreads to other parts of the body through bloodstream in patients with acute leukemia and recipients of tissue transplants. Clinical symptoms include pulmonary nodules and hemorrhage.","definition_xrefs":["DOID:0050073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary aspergilloma","termid":"MONDO:0000266"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"invasive aspergillosis","secondary_identifiers":["MEDGEN:922866","UMLS:C0238013","SCTID:721798004","icd11.foundation:1314810340"],"termid":"MONDO:0000240","xrefs":{"Monarch":{"xref_id":"0000240"}}}


id: GO:0002300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a CD8-positive, alpha-beta intraepithelial T cell. Intraepithelial T cells are found among epithelial cells in mucosal areas and have distinct phenotypes and developmental pathways.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-beta intraepithelial T cell differentiation","termid":"GO:0002299"},{"relation_name":"is_a","term_name":"CD8-positive, alpha-beta T cell differentiation","termid":"GO:0043374"}],"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":"CD8-positive, alpha-beta intraepithelial T cell differentiation","synonyms":[{"name":"CD8-positive, alpha-beta intraepithelial T cell development","type":"related"},{"name":"CD8-positive, alpha-beta intraepithelial T lymphocyte differentiation","type":"exact"},{"name":"CD8-positive, alpha-beta intraepithelial T-cell differentiation","type":"exact"},{"name":"CD8-positive, alpha-beta intraepithelial T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002300"}


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


id: PBO:0045130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA replication helicase/nuclease 2","termid":"PBO:0045130"}


id: PBO:0005783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate-CoA ligase beta subunit (predicted)","termid":"PBO:0005783"}


id: MONDO:0032925
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":"respiratory papillomatosis, juvenile recurrent, congenital","secondary_identifiers":["MEDGEN:1719353","OMIM:618803","UMLS:C5394112"],"synonyms":[{"name":"JRRP","type":"related"},{"name":"RESPIRATORY PAPILLOMATOSIS, JUVENILE RECURRENT, CONGENITAL","type":"related"}],"termid":"MONDO:0032925","xrefs":{"Monarch":{"xref_id":"0032925"}}}


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: MONDO:0016789
data:
  {"annotated_genes":["SJAG_04334","SJAG_00866","SJAG_03064","SJAG_02796","SJAG_02158","SJAG_03247","SJAG_01924","SJAG_00461","SJAG_00605","SJAG_03660","SJAG_02006","SJAG_04495","SJAG_03290","SJAG_04192","SJAG_02107","SJAG_02369","SJAG_03310","SJAG_00839","SJAG_03553","SJAG_02009"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86590,86591],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011534"},{"annotations":[84685,84687,84686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013046"},{"annotations":[86762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010392"},{"annotations":[85372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009865"},{"annotations":[85209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009295"},{"annotations":[85713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013275"},{"annotations":[86022,86021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011236"},{"annotations":[86174],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013762"},{"annotations":[86794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014674"},{"annotations":[84670,84671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007453"},{"annotations":[85690],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013877"},{"annotations":[85995,85996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009340"},{"annotations":[85942,85941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100165"},{"annotations":[85969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010717"},{"annotations":[85455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013580"},{"annotations":[86303],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009502"},{"annotations":[84741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009529"},{"annotations":[86304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009503"},{"annotations":[85967],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012120"},{"annotations":[85130],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009950"},{"annotations":[86706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007067"},{"annotations":[85322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014221"}]},"cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of pyruvate metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of amino acid and other organic acid metabolism","termid":"MONDO:0019189"},{"relation_name":"is_a","term_name":"inborn disorder of energy metabolism","termid":"MONDO:0019243"},{"relation_name":"is_a","term_name":"disorder of organic acid metabolism","termid":"MONDO:0045022"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00461":null,"SJAG_00605":null,"SJAG_00839":null,"SJAG_00866":null,"SJAG_01924":null,"SJAG_02006":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02158":null,"SJAG_02369":null,"SJAG_02796":null,"SJAG_03064":null,"SJAG_03247":null,"SJAG_03290":null,"SJAG_03310":null,"SJAG_03553":null,"SJAG_03660":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"pyruvate metabolism disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1842590","GARD:20752","Orphanet:254746","UMLS:C0268192"],"synonyms":[{"name":"inborn error of pyruvate metabolic process","type":"exact"},{"name":"inborn pyruvate metabolic process disorder","type":"exact"},{"name":"rare inborn error of pyruvate metabolic process","type":"exact"}],"termid":"MONDO:0016789","terms_by_termid":{"MONDO:0007067":null,"MONDO:0007453":null,"MONDO:0009295":null,"MONDO:0009340":null,"MONDO:0009502":null,"MONDO:0009503":null,"MONDO:0009529":null,"MONDO:0009865":null,"MONDO:0009950":null,"MONDO:0010392":null,"MONDO:0010717":null,"MONDO:0011236":null,"MONDO:0011534":null,"MONDO:0012120":null,"MONDO:0013046":null,"MONDO:0013275":null,"MONDO:0013580":null,"MONDO:0013762":null,"MONDO:0013877":null,"MONDO:0014221":null,"MONDO:0014674":null,"MONDO:0100165":null},"xrefs":{"Monarch":{"xref_id":"0016789"}}}


id: GO:0032427
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a GTPase protein binding domain (GDB) domain. The GBD is a short motif, including a minimum region of 16 amino acids, identified in proteins that bind to small GTPases such as Cdc42 and Rac.","definition_xrefs":["PMID:9119069","GOC:mah","GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"GBD domain binding","synonyms":[{"name":"CRIB motif binding","type":"exact"},{"name":"Cdc42/Rac interactive binding motif binding","type":"exact"},{"name":"P21-Rho-binding domain binding","type":"exact"},{"name":"PMD binding","type":"exact"}],"termid":"GO:0032427"}


id: PR:P41820
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- bfr1 gene.","definition_xrefs":["UniProtKB:P41820","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":"brefeldin A resistance protein Bfr1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18B5.01c","synonyms":[{"name":"SPCC18B5.01c","type":"related"},{"name":"Spom972h-bfr1","type":"exact"},{"name":"hba2","type":"related"}],"termid":"PR:P41820"}


id: PBO:0050546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HPS4 biogenesis of lysosomal organelles complex 3 subunit 2","termid":"PBO:0050546"}


id: PBO:0049494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 1","termid":"PBO:0049494"}


id: PBO:0079784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP glucuronosyltransferase family 1 member A5","termid":"PBO:0079784"}


id: GO:0100043
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that negatively regulates cellular response to alkaline pH.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cellular response to alkaline pH by transcription from RNA polymerase II promoter (obsolete GO:0100043)","termid":"GO:0100043"}


id: PBO:0011411
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-not_occurs_at","termid":"PBO:0011411"}


id: GO:0018707
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-phenanthrol + X-CH3 = X + 1-methoxyphenanthrene.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-phenanthrol methyltransferase activity (obsolete GO:0018707)","termid":"GO:0018707"}


id: FYPO:0002895
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 transcription occurs to a greater extent than normal during a cellular response to calcium ions. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription during vegetative growth","termid":"FYPO:0000780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000294","FYPO:0001320","FYPO:0006551","FYPO:0001985"],"is_obsolete":false,"name":"increased transcription during cellular response to calcium ion","synonyms":[{"name":"increased transcription during cellular response to calcium","type":"exact"},{"name":"increased transcription during cellular response to calcium ion during mitotic cell cycle","type":"related"},{"name":"increased transcription during cellular response to calcium ion during vegetative growth","type":"exact"},{"name":"increased transcription in response to calcium","type":"exact"}],"termid":"FYPO:0002895"}


id: PBO:0079935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"upstream transcription factor 1","termid":"PBO:0079935"}


id: PR:O60175
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein Hikeshi that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03201","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 OPI10 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21H7.06c","secondary_identifiers":["UniProtKB:O60175"],"synonyms":[{"name":"Spom972h-C11orf73","type":"exact"}],"termid":"PR:O60175"}


id: PBO:0055549
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 2985","termid":"PBO:0055549"}


id: PBO:0017615
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor Saf5","termid":"PBO:0017615"}


id: MONDO:0022851
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A severe form of Hallermann-Streiff syndrome, observed in one family. This is an n-of-1 use case where only one patient or family has been described with this disorder.","definition_xrefs":["PMID:8585575"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dennis-Fairhurst-Moore syndrome","secondary_identifiers":["GARD:290","UMLS:C2931775","MEDGEN:419158","Orphanet:2109","MESH:C538210"],"synonyms":[{"name":"Dennis Fairhurst Moore syndrome","type":"related"},{"name":"Hallermam Streiff like syndrome","type":"related"}],"termid":"MONDO:0022851","xrefs":{"Monarch":{"xref_id":"0022851"}}}


id: GO:2000084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mesenchymal to epithelial transition involved in mesonephros morphogenesis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell differentiation involved in kidney development","termid":"GO:2000696"},{"relation_name":"regulates","term_name":"mesenchymal to epithelial transition involved in mesonephros morphogenesis","termid":"GO:0061261"}],"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 mesenchymal to epithelial transition involved in mesonephros morphogenesis","synonyms":[{"name":"regulation of mesonephric mesenchyme to epithelial transition","type":"related"}],"termid":"GO:2000084"}


id: GO:0016025
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete proteasome endopeptidase regulator (obsolete GO:0016025)","synonyms":[{"name":"proteasome endopeptidase regulator","type":"exact"}],"termid":"GO:0016025"}


id: PBO:0116437
data:
  {"annotated_genes":["SJAG_04697"],"annotation_feature_type":"gene","cv_annotations":{"pombase_family_or_domain":[{"annotations":[56081],"is_not":false,"summary":null,"term":"PBO:0116437"}]},"cv_name":"pombase_family_or_domain","gene_count":1,"genes_by_uniquename":{"SJAG_04697":null},"genotype_count":0,"is_obsolete":false,"name":"warning frameshifted","termid":"PBO:0116437","terms_by_termid":{"PBO:0116437":null}}


id: PBO:0113321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase; implicated in activation of the plasma membrane H(+)-ATPase Pma1p in response to glucose metabolism and under acetic acid stress; plays a role in ion homeostasis; maintains pH homeostasis and modulates plasma membrane potential under acetic acid stress; protein abundance increases in response to DNA replication stress","termid":"PBO:0113321"}


id: PBO:0073163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC63 homolog, protein translocation regulator","termid":"PBO:0073163"}


id: MOD:01893
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-malonyl-L-lysine.","definition_xrefs":["PubMed:8349414","PubMed:21908771","RESID:AA0568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"N6-malonyl-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-[(carboxyacetyl)amino]hexanoic acid","type":"exact"},{"name":"2-azanyl-6-[(carboxyacetyl)azanyl]hexanoic acid","type":"exact"},{"name":"MOD_RES N6-malonyllysine","type":"exact"},{"name":"N(epsilon)-(malonyl)lysine","type":"exact"},{"name":"N6-(carboxyacetyl)lysine","type":"exact"},{"name":"N6-malonyl-L-lysine","type":"exact"},{"name":"N6-malonyllysine","type":"exact"},{"name":"malonyllysine","type":"exact"}],"termid":"MOD:01893"}


id: PBO:0047811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box M1","termid":"PBO:0047811"}


id: PBO:0045333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DOCK8 antisense RNA 2","termid":"PBO:0045333"}


id: MONDO:0004539
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the aorta.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"vascular cancer","termid":"MONDO:0002095"},{"relation_name":"is_a","term_name":"aortic disorder","termid":"MONDO:0005561"},{"relation_name":"is_a","term_name":"great vessel cancer","termid":"MONDO:0040676"}],"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":"aortic malignant tumor","secondary_identifiers":["DOID:8352","UMLS:C1334560","NCIT:C5375","MEDGEN:235290"],"synonyms":[{"name":"aorta cancer","type":"exact"},{"name":"aortic malignant neoplasm","type":"exact"},{"name":"cancer of aorta","type":"exact"},{"name":"malignant aorta neoplasm","type":"exact"},{"name":"malignant aortic neoplasm","type":"exact"},{"name":"malignant neoplasm of aorta","type":"exact"},{"name":"malignant neoplasm of the aorta","type":"exact"},{"name":"malignant tumor of aorta","type":"exact"},{"name":"malignant tumor of the aorta","type":"exact"},{"name":"malignant tumour of aorta","type":"exact"},{"name":"malignant tumour of the aorta","type":"exact"}],"termid":"MONDO:0004539","xrefs":{"Monarch":{"xref_id":"0004539"}}}


id: PBO:0003068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase I transcription termination factor Reb1","termid":"PBO:0003068"}


id: MONDO:8000018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic recurrent vertigo associated with positional nystagmus. It is associated with a vestibular loss without other neurological or auditory signs. Unlike in labyrinthitis and vestibular neuronitis inflammation in the ear is not observed.","definition_xrefs":["MESH:D065635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral vertigo","termid":"MONDO:0004900"},{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"},{"relation_name":"is_a","term_name":"inherited auditory system disease","termid":"MONDO:0037940"},{"relation_name":"is_a","term_name":"hereditary neuromuscular disease","termid":"MONDO:0100546"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign paroxysmal positional vertigo","secondary_identifiers":["UMLS:C0155502","MEDGEN:57837","OMIM:193007","DOID:13941","ICD9:386.11","SCTID:111541001"],"synonyms":[{"name":"BPPV","type":"exact"},{"name":"BRV","type":"exact"},{"name":"benign paroxysmal positional nystagmus","type":"exact"},{"name":"benign paroxysmal positional vertigo","type":"exact"},{"name":"familial benign recurrent vertigo","type":"exact"},{"name":"familial vestibulopathy","type":"exact"},{"name":"vertigo, benign paroxysmal positional","type":"exact"},{"name":"vertigo, benign recurrent","type":"exact"},{"name":"vestibulopathy, familial","type":"exact"}],"termid":"MONDO:8000018","xrefs":{"Monarch":{"xref_id":"8000018"}}}


id: PBO:0067859
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 161","termid":"PBO:0067859"}


id: PBO:0058899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 12117","termid":"PBO:0058899"}


id: MONDO:0007179
data:
  {"annotated_genes":["SJAG_01787","SJAG_03850","SJAG_04810","SJAG_00610","SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86179],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013767"},{"annotations":[85349,85350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000024"},{"annotations":[86060],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008218"},{"annotations":[85712],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013276"}]},"cv_name":"mondo","definition":"A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis).","definition_xrefs":["NCIT:C2889"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hypersensitivity reaction disease","termid":"MONDO:0000605"},{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_03453":null,"SJAG_03850":null,"SJAG_04810":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:279.49","UMLS:C0004364","MEDGEN:2135","OMIM:109100","DOID:417","MESH:D001327","SCTID:85828009","ICD9:279.4","EFO:0005809","ICD9:720","OBI:1110054"],"synonyms":[{"name":"autoimmune disease","type":"exact"},{"name":"autoimmune disease or disorder","type":"exact"},{"name":"autoimmune disorder","type":"exact"},{"name":"autoimmune hypersensitivity disease","type":"related"},{"name":"disease, autoimmune","type":"exact"},{"name":"hypersensitivity reaction type II disease","type":"related"}],"termid":"MONDO:0007179","terms_by_termid":{"MONDO:0008218":null,"MONDO:0013276":null,"MONDO:0013767":null,"MONDO:8000024":null},"xrefs":{"Monarch":{"xref_id":"0007179"}}}


id: MONDO:0700230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any foveal hypoplasia with or without albinism caused by a variant in the GPR143 gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"foveal hypoplasia","termid":"MONDO:0044203"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPR143-related foveal hypoplasia","synonyms":[{"name":"GPR143-related foveal hypoplasia with or without albinism","type":"exact"}],"termid":"MONDO:0700230","xrefs":{"Monarch":{"xref_id":"0700230"}}}


id: PBO:0071658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L37a","termid":"PBO:0071658"}


id: MONDO:0012572
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":"Sakoda complex","secondary_identifiers":["MEDGEN:370271","UMLS:C1970485","MESH:C567055","OMIM:610871"],"synonyms":[{"name":"Sakoda complex","type":"exact"},{"name":"Sakoda spectrum","type":"related"},{"name":"sphenoethmoidal encephalomeningocele agenesis of the corpus callosum and cleft lip/palate","type":"related"},{"name":"sphenoethmoidal encephalomeningocele, agenesis of the corpus callosum, and cleft Lip/palate","type":"related"}],"termid":"MONDO:0012572","xrefs":{"Monarch":{"xref_id":"0012572"}}}


id: PBO:0076411
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 6","termid":"PBO:0076411"}


id: SO:0000938
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration.","direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immune_system_gene_recombination_feature","termid":"SO:0000301"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_gene_cluster","synonyms":[{"name":"vertebrate immunoglobulin T cell receptor rearranged gene cluster","type":"exact"}],"termid":"SO:0000938"}


id: PBO:0042463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell division cycle associated 4","termid":"PBO:0042463"}


id: PBO:0064534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit K pseudogene 2","termid":"PBO:0064534"}


id: MONDO:0008473
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare type of spondyloepiphyseal dysplasia described in fewer than 10 patients to date and characterized clinically by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, scoliosis, genu valgum, abnormal pelvis, osteoporosis and osteoarthritis.","definition_xrefs":["Orphanet:263482"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"},{"relation_name":"is_a","term_name":"TRPV4-related bone disorder","termid":"MONDO:0018240"},{"relation_name":"is_a","term_name":"spondyloepimetaphyseal dysplasia","termid":"MONDO:0100510"}],"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":"spondyloepimetaphyseal dysplasia, Maroteaux type","secondary_identifiers":["MEDGEN:463613","OMIM:184095","SCTID:719204007","DOID:0111553","GARD:994","UMLS:C3159322"],"synonyms":[{"name":"SED, Maroteaux type","type":"exact"},{"name":"brachyolmia Maroteaux type","type":"related"},{"name":"pseudo-Morquio syndrome type 2","type":"exact"},{"name":"pseudo-Morquio syndrome, type 2","type":"related"},{"name":"spondyloepimetaphyseal dysplasia, Maroteaux type","type":"exact"},{"name":"spondyloepiphyseal dysplasia Maroteaux type","type":"exact"},{"name":"spondyloepiphyseal dysplasia, Maroteaux type","type":"exact"}],"termid":"MONDO:0008473","xrefs":{"Monarch":{"xref_id":"0008473"}}}


id: MONDO:0006103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sporadic or familial pheochromocytoma that is confined to the adrenal gland and does not have any metastatic potential. The majority of cases are sporadic, and usually unilateral. Familial cases are usually bilateral.","definition_xrefs":["NCIT:C48305"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adrenal gland pheochromocytoma","termid":"MONDO:0004974"},{"relation_name":"is_a","term_name":"benign neoplasm of adrenal medulla","termid":"MONDO:0021468"},{"relation_name":"is_a","term_name":"benign epithelial neoplasm","termid":"MONDO:0036976"},{"relation_name":"is_a","term_name":"benign neoplasm of peripheral nervous system","termid":"MONDO:0056804"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign adrenal gland pheochromocytoma","secondary_identifiers":["EFO:1000106","MEDGEN:317403","UMLS:C1706920"],"synonyms":[{"name":"adrenal gland pheochromocytoma, benign","type":"exact"},{"name":"benign adrenal gland pheochromocytoma","type":"exact"},{"name":"pheochromocytoma, benign","type":"exact"}],"termid":"MONDO:0006103","xrefs":{"Monarch":{"xref_id":"0006103"}}}


id: MONDO:0020610
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete blood group, diego system (obsolete MONDO:0020610)","secondary_identifiers":["OMIM:110500"],"synonyms":[{"name":"BLOOD GROUP, DIEGO SYSTEM","type":"related"},{"name":"DI","type":"related"},{"name":"Diego Blood Group System","type":"related"},{"name":"blood group, Diego","type":"exact"}],"termid":"MONDO:0020610","xrefs":{"Monarch":{"xref_id":"0020610"}}}


id: PBO:0042444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC42EP3 antisense RNA 1","termid":"PBO:0042444"}


id: PBO:0080083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 45","termid":"PBO:0080083"}


id: MONDO:0013260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"eosinophilic esophagitis","termid":"MONDO:0005361"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"esophagitis, eosinophilic, 2","secondary_identifiers":["OMIM:613412","UMLS:C3150679","MEDGEN:462029"],"synonyms":[{"name":"EOE2","type":"exact"},{"name":"esophagitis, eosinophilic, 2","type":"exact"}],"termid":"MONDO:0013260","xrefs":{"Monarch":{"xref_id":"0013260"}}}


id: PBO:0045777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ECSIT signaling integrator","termid":"PBO:0045777"}


id: PBO:0057731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1306","termid":"PBO:0057731"}


id: MONDO:0010928
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":"dwarfism, familial, with muscle spasms","secondary_identifiers":["MEDGEN:322168","UMLS:C1833341","OMIM:600771","MESH:C563447"],"synonyms":[{"name":"dwarfism familial with muscle spasms","type":"related"},{"name":"dwarfism, familial, with muscle spasms","type":"exact"},{"name":"familial dwarfism and painful muscle spasms","type":"related"}],"termid":"MONDO:0010928","xrefs":{"Monarch":{"xref_id":"0010928"}}}


id: MONDO:0016770
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Actinic lichen planus (LP) is a rare variant of cutaneous lichen planus characterized by the development of photo-distributed lichenoid lesions.","definition_xrefs":["Orphanet:254395"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lichen planus","termid":"MONDO:0006572"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"actinic lichen planus","secondary_identifiers":["icd11.foundation:365229579","MEDGEN:590348","SCTID:200999007","UMLS:C0406365","GARD:12673"],"synonyms":[{"name":"actinic LP","type":"exact"},{"name":"lichen planus actinus","type":"exact"},{"name":"lichen planus subtropicus","type":"exact"},{"name":"lichen planus tropicus","type":"exact"},{"name":"lichenoid melanodermatitis","type":"exact"},{"name":"summertime actinic lichenoid eruption","type":"exact"}],"termid":"MONDO:0016770","xrefs":{"Monarch":{"xref_id":"0016770"}}}


id: PBO:0109388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 17C","termid":"PBO:0109388"}


id: GO:0062156
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the ATP-dependent diffusion of a potassium ion across the mitochondrial inner membrane.","definition_xrefs":["PMID:31435016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium channel activity","termid":"GO:0005267"},{"relation_name":"is_a","term_name":"ATP-gated ion channel activity","termid":"GO:0035381"},{"relation_name":"is_a","term_name":"ligand-gated monoatomic cation channel activity","termid":"GO:0099094"}],"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:0005215","GO:0022857"],"is_obsolete":false,"name":"mitochondrial ATP-gated potassium channel activity","synonyms":[{"name":"mitoK-ATP activity","type":"exact"},{"name":"mitochondrial potassium channel activity","type":"exact"}],"termid":"GO:0062156"}


id: MONDO:0017441
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital malformation in which the upper portion of a limb is either shortened or absent.","definition_xrefs":["NCIT:C34928"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"}],"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":"congenital absence of upper arm and forearm with hand present","secondary_identifiers":["GARD:12123","Orphanet:294975","MEDGEN:539337","SCTID:22841008","UMLS:C0265574","ICD10CM:Q71.1","icd11.foundation:1157109358"],"synonyms":[{"name":"humero-radio-ulnar intercalary transverse meromelia","type":"exact"},{"name":"phocomelia","type":"exact"}],"termid":"MONDO:0017441","xrefs":{"Monarch":{"xref_id":"0017441"}}}


id: GO:1900024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of substrate adhesion-dependent cell spreading.","definition_xrefs":["GOC:yaf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell-substrate adhesion","termid":"GO:0010810"},{"relation_name":"regulates","term_name":"substrate adhesion-dependent cell spreading","termid":"GO:0034446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"regulation of substrate adhesion-dependent cell spreading","synonyms":[{"name":"regulation of cell spreading during cell substrate adhesion","type":"exact"},{"name":"regulation of substrate adhesion dependent cell spreading","type":"exact"}],"termid":"GO:1900024"}


id: PBO:0013476
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trichostatin A suppresses accumulation of septated cells, but does not restore wild-type checkpoint function, in chk1delta mutant","termid":"PBO:0013476"}


id: GO:1901871
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ecgonone methyl ester.","definition_xrefs":["PMID:22665766","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkaloid catabolic process","termid":"GO:0009822"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"ecgonone methyl ester metabolic process","termid":"GO:1901870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"ecgonone methyl ester catabolic process","synonyms":[{"name":"ecgonone methyl ester breakdown","type":"exact"},{"name":"ecgonone methyl ester catabolism","type":"exact"},{"name":"ecgonone methyl ester degradation","type":"exact"}],"termid":"GO:1901871"}


id: PBO:0065219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosyl pyrophosphate synthetase associated protein 2","termid":"PBO:0065219"}


id: SO:0000760
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000760 YAC_clone (obsolete SO:0000760)","termid":"SO:0000760"}


id: FYPO:0007572
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the cortical endoplasmic reticulum (ER) is dissociated from the plasma membrane. Normally, cortical ER tubules are closely juxtaposed to the plasma membrane.","definition_xrefs":["PMID:19571115","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal endoplasmic reticulum morphology","termid":"FYPO:0000354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"cortical endoplasmic reticulum detached from plasma membrane","synonyms":[{"name":"cortical ER detached from plasma membrane","type":"exact"},{"name":"cortical endoplasmic reticulum detached from plasma membrane during mitotic cell cycle","type":"related"},{"name":"cortical endoplasmic reticulum detached from plasma membrane during vegetative growth","type":"exact"},{"name":"cortical endoplasmic reticulum dissociated from plasma membrane","type":"exact"}],"termid":"FYPO:0007572"}


id: GO:1900792
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of shamixanthone.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"secondary metabolite catabolic process","termid":"GO:0090487"},{"relation_name":"is_a","term_name":"shamixanthone metabolic process","termid":"GO:1900791"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0019748","GO:0008150"],"is_obsolete":false,"name":"shamixanthone catabolic process","synonyms":[{"name":"shamixanthone breakdown","type":"exact"},{"name":"shamixanthone catabolism","type":"exact"},{"name":"shamixanthone degradation","type":"exact"}],"termid":"GO:1900792"}


id: PBO:0005743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin Npp106","termid":"PBO:0005743"}


id: PBO:0114090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F1-FO ATP synthase peripheral stalk subunit OSCP Atp5","termid":"PBO:0114090"}


id: GO:1902823
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of late endosome to lysosome transport.","definition_xrefs":["GOC:PARL","GOC:pad","GOC:TermGenie","GO_REF:0000058","PMID:23949442"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of late endosome to lysosome transport","termid":"GO:1902822"},{"relation_name":"is_a","term_name":"negative regulation of vacuolar transport","termid":"GO:1903336"},{"relation_name":"negatively_regulates","term_name":"late endosome to lysosome transport","termid":"GO:1902774"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of late endosome to lysosome transport","synonyms":[{"name":"down regulation of late endosome to lysosome transport","type":"exact"},{"name":"down-regulation of late endosome to lysosome transport","type":"exact"},{"name":"downregulation of late endosome to lysosome transport","type":"exact"},{"name":"inhibition of late endosome to lysosome transport","type":"narrow"}],"termid":"GO:1902823"}


id: PBO:0089059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-type ATPase V1 domain subunit G","termid":"PBO:0089059"}


id: PBO:0055925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 37 member A13, pseudogene","termid":"PBO:0055925"}


id: GO:0002317
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a B cell acquires the specialized features of a plasma cell. A plasma cell is a lymphocyte which develops from a B cell and produces high amounts of antibody.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mature B cell differentiation involved in immune response","termid":"GO:0002313"}],"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":"plasma cell differentiation","synonyms":[{"name":"plasma cell development","type":"related"}],"termid":"GO:0002317"}


id: PBO:0086673
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; identified by fungal homology comparisons and RT-PCR; partially overlaps RND5-5; YLR159C-A has a paralog, YLR156C-A, that arose from a segmental duplication","termid":"PBO:0086673"}


id: GO:1904234
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of aconitate hydratase activity.","definition_xrefs":["GO_REF:0000059","GOC:rl","GOC:TermGenie","GOC:BHF","PMID:18160053"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lyase activity","termid":"GO:0051349"}],"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 aconitate hydratase activity","synonyms":[{"name":"activation of aconitase activity","type":"narrow"},{"name":"activation of aconitate hydratase activity","type":"narrow"},{"name":"activation of cis-aconitase activity","type":"narrow"},{"name":"activation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"narrow"},{"name":"activation of citrate(isocitrate) hydro-lyase activity","type":"narrow"},{"name":"positive regulation of aconitase activity","type":"exact"},{"name":"positive regulation of cis-aconitase activity","type":"exact"},{"name":"positive regulation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"exact"},{"name":"positive regulation of citrate(isocitrate) hydro-lyase activity","type":"exact"},{"name":"up regulation of aconitase activity","type":"exact"},{"name":"up regulation of aconitate hydratase activity","type":"exact"},{"name":"up regulation of cis-aconitase activity","type":"exact"},{"name":"up regulation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"exact"},{"name":"up regulation of citrate(isocitrate) hydro-lyase activity","type":"exact"},{"name":"up-regulation of aconitase activity","type":"exact"},{"name":"up-regulation of aconitate hydratase activity","type":"exact"},{"name":"up-regulation of cis-aconitase activity","type":"exact"},{"name":"up-regulation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"exact"},{"name":"up-regulation of citrate(isocitrate) hydro-lyase activity","type":"exact"},{"name":"upregulation of aconitase activity","type":"exact"},{"name":"upregulation of aconitate hydratase activity","type":"exact"},{"name":"upregulation of cis-aconitase activity","type":"exact"},{"name":"upregulation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"exact"},{"name":"upregulation of citrate(isocitrate) hydro-lyase activity","type":"exact"}],"termid":"GO:1904234"}


id: PBO:0079309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 4B","termid":"PBO:0079309"}


id: FYPO:0007232
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which regulation of the initiation of mitotic DNA replication from early-firing origins is abnormal.","definition_xrefs":["PMID:22279046","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of mitotic DNA replication initiation","termid":"FYPO:0001248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000631","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal regulation of mitotic DNA replication initiation from early origin","synonyms":[{"name":"abnormal regulation of DNA replication initiation from early origin during mitotic cell cycle","type":"related"},{"name":"abnormal regulation of early origin firing timing","type":"related"},{"name":"abnormal regulation of mitotic DNA replication initiation at early origin","type":"exact"},{"name":"abnormal regulation of mitotic DNA replication initiation from early origin during vegetative growth","type":"exact"},{"name":"abnormal regulation of mitotic DNA replication initiation from early replication origin","type":"exact"}],"termid":"FYPO:0007232"}


id: MOD:00553
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes a (2-sulfanylethyl)sulfanyl (or thioethylthiol) group for a hydroxy group.","definition_xrefs":["Unimod:200","DeltaMass:0","PubMed:11507762"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1,2-ethanedithiol modified residue","synonyms":[{"name":"1,2-ethanedithiol (EDT)","type":"exact"},{"name":"EDT","type":"related"},{"name":"Ethanedithiol","type":"related"}],"termid":"MOD:00553"}


id: GO:1990236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the proteasome core complex (AKA core particle (CP)) from the cytoplasm into the nucleus.","definition_xrefs":["GOC:rb","PMID:23982732","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex localization","termid":"GO:0031503"},{"relation_name":"is_a","term_name":"import into nucleus","termid":"GO:0051170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006913"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0006913"],"is_obsolete":false,"name":"proteasome core complex import into nucleus","termid":"GO:1990236"}


id: PBO:0060588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBR1 autophagy cargo receptor","termid":"PBO:0060588"}


id: PBO:0029843
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_acetylation","termid":"PBO:0029843"}


id: GO:0061916
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"That part of the axonal growth cone which represents the distal part of the structure.","definition_xrefs":["PMID:16098134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth cone leading edge","termid":"GO:0061850"},{"relation_name":"part_of","term_name":"axonal growth cone","termid":"GO:0044295"}],"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":"leading edge of axonal growth cone","synonyms":[{"name":"axonal growth cone leading edge","type":"exact"},{"name":"distal tip of axonal growth cone","type":"exact"}],"termid":"GO:0061916"}


id: MOD:00458
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a 4x(2)H labeled succinyl group.","definition_xrefs":["Unimod:65#N-term","PubMed:11857757","PubMed:12175151"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-amino succinylated residue","termid":"MOD:00457"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4x(2)H labeled alpha-amino succinylated residue","synonyms":[{"name":"Succinic anhydride labeling reagent, heavy form (+4amu, 4H2), N-term","type":"related"},{"name":"Succinyl:2H(4)","type":"related"}],"termid":"MOD:00458"}


id: PBO:0038996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AE binding protein 2","termid":"PBO:0038996"}


id: MONDO:0030506
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46 XX gonadal dysgenesis","termid":"MONDO:0009299"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"ovarian dysgenesis 9","secondary_identifiers":["MEDGEN:1794256","UMLS:C5562046","OMIM:619665"],"synonyms":[{"name":"ODG9","type":"exact"}],"termid":"MONDO:0030506","xrefs":{"Monarch":{"xref_id":"0030506"}}}


id: MONDO:0009963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ulbright-Hodes syndrome is characterized by renal dysplasia, growth retardation, phocomelia or mesomelia, radiohumeral fusion, rib abnormalities, anomalies of the external genitalia and a potter-like facies. The syndrome has been described in three infants (one pair of sibs and an unrelated case), all of whom died shortly after birth from respiratory distress resulting from pulmonary hypoplasia and oligohydramnios caused by renal dysplasia. The mode of transmission appears to be autosomal recessive.","definition_xrefs":["Orphanet:3404"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ulbright-Hodes syndrome","secondary_identifiers":["OMIM:266910","SCTID:719840003","MEDGEN:376585","UMLS:C1849438","GARD:5394","MESH:C537754"],"synonyms":[{"name":"RL syndrome","type":"related"},{"name":"Ulbright Hodes syndrome","type":"related"},{"name":"renal dysplasia limb defects syndrome","type":"related"},{"name":"renal dysplasia, mesomelia, and radiohumeral fusion","type":"related"},{"name":"renal dysplasia-limb defects syndrome","type":"exact"},{"name":"renal dysplasia-mesomelia-radiohumeral fusion syndrome","type":"exact"}],"termid":"MONDO:0009963","xrefs":{"Monarch":{"xref_id":"0009963"}}}


id: SOFP:mol_type
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","definition":"The type of molecule","definition_xrefs":["so:sjc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mol_type","termid":"SOFP:mol_type"}


id: GO:1904445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of establishment of Sertoli cell barrier.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:18057314"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell development","termid":"GO:0010721"},{"relation_name":"is_a","term_name":"negative regulation of epithelial cell differentiation","termid":"GO:0030857"},{"relation_name":"is_a","term_name":"regulation of establishment of Sertoli cell barrier","termid":"GO:1904444"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"negatively_regulates","term_name":"establishment of Sertoli cell barrier","termid":"GO:0097368"}],"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 establishment of Sertoli cell barrier","synonyms":[{"name":"down regulation of establishment of BTB","type":"exact"},{"name":"down regulation of establishment of SCB","type":"exact"},{"name":"down regulation of establishment of Sertoli cell barrier","type":"exact"},{"name":"down regulation of establishment of blood-testis barrier","type":"exact"},{"name":"down-regulation of establishment of BTB","type":"exact"},{"name":"down-regulation of establishment of SCB","type":"exact"},{"name":"down-regulation of establishment of Sertoli cell barrier","type":"exact"},{"name":"down-regulation of establishment of blood-testis barrier","type":"exact"},{"name":"downregulation of establishment of BTB","type":"exact"},{"name":"downregulation of establishment of SCB","type":"exact"},{"name":"downregulation of establishment of Sertoli cell barrier","type":"exact"},{"name":"downregulation of establishment of blood-testis barrier","type":"exact"},{"name":"inhibition of establishment of BTB","type":"narrow"},{"name":"inhibition of establishment of SCB","type":"narrow"},{"name":"inhibition of establishment of Sertoli cell barrier","type":"narrow"},{"name":"inhibition of establishment of blood-testis barrier","type":"narrow"},{"name":"negative regulation of establishment of BTB","type":"exact"},{"name":"negative regulation of establishment of SCB","type":"exact"},{"name":"negative regulation of establishment of blood-testis barrier","type":"exact"}],"termid":"GO:1904445"}


id: MONDO:0006548
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Facial Dermatosis, also known as facial dermatoses, is related tolipogranulomatosis. An important gene associated with Facial Dermatosis isCCNE1(cyclin E1). The drugsbetamethasoneandbetamethasone acetatehave been mentioned in the context of this disorder.","definition_xrefs":["EFO:1000698"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"facial dermatosis","secondary_identifiers":["DOID:3134","MEDGEN:8760","MESH:D005148","UMLS:C0015456"],"termid":"MONDO:0006548","xrefs":{"Monarch":{"xref_id":"0006548"}}}


id: PBO:0083866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box component of an SCF ubiquitin protein ligase complex; associates with and is required for Fzo1p ubiquitination and for mitochondria fusion; stimulates nuclear export of specific mRNAs; promotes ubiquitin-mediated degradation of Gal4p in some strains","termid":"PBO:0083866"}


id: GO:0009327
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex that possesses NAD(P)+ transhydrogenase (AB-specific) activity. Homodimeric, trimeric, and heterotetrameric complexes have been identified.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete NAD(P)+ transhydrogenase complex (AB-specific) (obsolete GO:0009327)","termid":"GO:0009327"}


id: PBO:0077677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF superfamily member 8","termid":"PBO:0077677"}


id: PBO:0085294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pheromone-regulated protein; contains 3 predicted transmembrane segments and an FF sequence, a motif involved in COPII binding; member of DUP240 gene family; PRM9 has a paralog, PRM8, that arose from a segmental duplication","termid":"PBO:0085294"}


id: MOD:01371
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE bcecause identical and redundant with MOD:00851. Remap to MOD:00851.","definition_xrefs":["PubMed:8382902"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01371 deamidation in presence of O18 (obsolete MOD:01371)","synonyms":[{"name":"Deamidated:18O(1)","type":"related"},{"name":"Deamidation in presence of O18","type":"related"}],"termid":"MOD:01371"}


id: PBO:0034718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipid particle hydrolase (predicted)","termid":"PBO:0034718"}


id: GO:0021533
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the mature cells of the hindbrain. Differentiation includes the processes involved in commitment of a cell to a specific fate.","definition_xrefs":["GOC:dgh","GO_REF:0000021","GOC:dph","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"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":"cell differentiation in hindbrain","termid":"GO:0021533"}


id: PBO:0074197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 39 member 7","termid":"PBO:0074197"}


id: GO:0008726
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an alkanesulfonate + O2 + FMNH2 = an aldehyde + sulfite + H2O + FMN.","definition_xrefs":["MetaCyc:RXN0-280"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"alkanesulfonate monooxygenase activity","secondary_identifiers":["RHEA:23064","EC:1.14.14.5"],"synonyms":[{"name":"FMNH(2)-dependent aliphatic sulfonate monooxygenase activity","type":"related"},{"name":"FMNH(2)-dependent alkanesulfonate monooxygenase activity","type":"exact"},{"name":"FMNH2-dependent aliphatic sulfonate monooxygenase activity","type":"related"},{"name":"SsuD","type":"related"},{"name":"alkanesulfonate, reduced-FMN:oxygen oxidoreductase activity","type":"related"},{"name":"alkanesulphonate monooxygenase activity","type":"exact"},{"name":"sulfate starvation-induced protein 6 activity","type":"related"}],"termid":"GO:0008726"}


id: MONDO:0017593
data:
  {"annotated_genes":["SJAG_03598"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013715"}]},"cv_name":"mondo","definition":"Juvenile amyotrophic lateral sclerosis (JALS) is a very rare severe motor neuron disease characterized by progressive upper and lower motor neuron degeneration causing facial spasticity, dysarthria, and gait disorders with onset before 25 years of age.","definition_xrefs":["Orphanet:300605"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03598":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"juvenile amyotrophic lateral sclerosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:11901","MEDGEN:923704","UMLS:C3468114","SCTID:718555006"],"synonyms":[{"name":"JALS","type":"exact"},{"name":"amyotrophic lateral sclerosis, juvenile","type":"related"},{"name":"juvenile Charcot disease","type":"exact"},{"name":"juvenile Lou Gehrig disease","type":"exact"}],"termid":"MONDO:0017593","terms_by_termid":{"MONDO:0013715":null},"xrefs":{"Monarch":{"xref_id":"0017593"}}}


id: GO:0014911
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of smooth muscle cell migration.","definition_xrefs":["CL:0000192","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of smooth muscle cell migration","termid":"GO:0014910"},{"relation_name":"is_a","term_name":"positive regulation of cell migration","termid":"GO:0030335"},{"relation_name":"positively_regulates","term_name":"smooth muscle cell migration","termid":"GO:0014909"}],"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 smooth muscle cell migration","termid":"GO:0014911"}


id: PBO:0060536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetyltransferase 16 (putative)","termid":"PBO:0060536"}


id: PBO:0072323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 9","termid":"PBO:0072323"}


id: GO:0039535
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the RIG-I signaling pathway.","definition_xrefs":["GOC:bf","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039531"},{"relation_name":"regulates","term_name":"RIG-I signaling pathway","termid":"GO:0039529"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of RIG-I signaling pathway","synonyms":[{"name":"regulation of DDX58 signaling pathway","type":"exact"},{"name":"regulation of RIG-I signalling pathway","type":"exact"},{"name":"regulation of retinoic acid inducible gene I signaling pathway","type":"exact"}],"termid":"GO:0039535"}


id: PR:O14206
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A suppressor of SWI4 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01002","PANTHER:PTHR12661:SF3"],"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":"brix domain-containing protein C1B9.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B9.03c","secondary_identifiers":["UniProtKB:O14206"],"synonyms":[{"name":"Spom972h-PPAN","type":"exact"}],"termid":"PR:O14206"}


id: PBO:0071783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein lateral stalk subunit P0 pseudogene 11","termid":"PBO:0071783"}


id: PR:P87179
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- wsc1 gene.","definition_xrefs":["UniProtKB:P87179","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":"cell wall integrity and stress response component 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC30B4.01c","synonyms":[{"name":"Spom972h-wsc1","type":"exact"}],"termid":"PR:P87179"}


id: GO:0051219
data:
  {"annotated_genes":["SJAG_03118","SJAG_04933"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72026,77617],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990269"}]},"cv_name":"molecular_function","definition":"Binding to a phosphorylated protein.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03118":null,"SJAG_04933":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"phosphoprotein binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"phosphorylated protein binding","type":"exact"}],"termid":"GO:0051219","terms_by_termid":{"GO:1990269":null}}


id: PBO:0003331
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cockayne syndrome","termid":"PBO:0003331"}


id: GO:0140677
data:
  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id: GO:0047824
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-iditol + NAD+ = D-sorbose + NADH.","definition_xrefs":["RHEA:12725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"},{"relation_name":"is_a","term_name":"hexitol dehydrogenase activity","termid":"GO:0031320"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"D-iditol 2-dehydrogenase activity","secondary_identifiers":["MetaCyc:D-IDITOL-2-DEHYDROGENASE-RXN"],"termid":"GO:0047824"}


id: PBO:0053625
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  {"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 668","termid":"PBO:0053625"}


id: MONDO:0017324
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive hypophosphatemic rickets (ARHR) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia and slow growth.","definition_xrefs":["Orphanet:289176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hypophosphatemic rickets","termid":"MONDO:0000044"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"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":"autosomal recessive hypophosphatemic rickets","secondary_identifiers":["DOID:0050949","ICD10CM:E83.3","GARD:17320","MEDGEN:137975","SCTID:90505000","UMLS:C0342643"],"synonyms":[{"name":"ARHR","type":"exact"},{"name":"autosomal recessive hereditary hypophosphatemic rickets","type":"exact"},{"name":"hereditary hypophosphatemic rickets, autosomal recessive","type":"exact"},{"name":"hypophosphatemic rickets, autosomal recessive","type":"exact"}],"termid":"MONDO:0017324","xrefs":{"Monarch":{"xref_id":"0017324"}}}


id: PBO:0070497
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5 pseudogene 32","termid":"PBO:0070497"}


id: MONDO:0956964
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A medulloblastoma SHH activated that is characterized as a molecular subtype by activation of the sonic hedgehog (SHH) pathway and the presence of TP53 mutations.","definition_xrefs":["DOID:0080704"],"direct_ancestors":[{"relation_name":"is_a","term_name":"medulloblastoma SHH activated","termid":"MONDO:0850197"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"medulloblastoma SHH activated and TP53 mutant","termid":"MONDO:0956964","xrefs":{"Monarch":{"xref_id":"0956964"}}}


id: GO:0030146
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of renal water excretion.","definition_xrefs":["GOC:mtg_cardio","ISBN:0198506732","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete diuresis (obsolete GO:0030146)","secondary_identifiers":["Wikipedia:Diuresis"],"synonyms":[{"name":"diuresis","type":"exact"},{"name":"positive regulation of renal water excretion","type":"exact"},{"name":"renal water excretion","type":"broad"}],"termid":"GO:0030146"}


id: PBO:0030965
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id: GO:0097118
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The receptor clustering process involved in assembly of the postsynaptic membrane in which neuroligins are localized to distinct domains in the cell membrane. Neuroligins are neuronal cell surface proteins on the postsynaptic membrane that mediate synapse formation between neurons.","definition_xrefs":["PMID:12796785","GOC:BHF","GOC:sjp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor clustering","termid":"GO:0043113"},{"relation_name":"part_of","term_name":"postsynaptic membrane assembly","termid":"GO:0097104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150","GO:0044085","GO:0051179"],"is_obsolete":false,"name":"neuroligin clustering involved in postsynaptic membrane assembly","synonyms":[{"name":"Nlgn clustering","type":"broad"},{"name":"neuroligin clustering","type":"broad"},{"name":"postsynaptic neuroligin clustering","type":"exact"}],"termid":"GO:0097118"}


id: MONDO:0800121
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An interstitial lung disease specific to infancy that is characterized by tachypnea at birth and persistent disease, diffuse interstitial thickening due to pale oval and spindle-shaped histiocytes without scarring.","definition_xrefs":["PMID:1555422"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interstitial lung disease specific to infancy","termid":"MONDO:0017019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cellular interstitial pneumonitis","termid":"MONDO:0800121","xrefs":{"Monarch":{"xref_id":"0800121"}}}


id: MONDO:0004929
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disease of orbital part of eye adnexa","termid":"MONDO:0004751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"constant exophthalmos","secondary_identifiers":["icd11.foundation:2100094996","ICD9:376.31","DOID:9945","SCTID:89907009","UMLS:C0155267","MEDGEN:509884"],"termid":"MONDO:0004929","xrefs":{"Monarch":{"xref_id":"0004929"}}}


id: MONDO:0012495
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare primary bone dysplasia characterized by severe developmental delay and skeletal dysplasia (including short stature, premature carpal ossification, platyspondyly, longitudinal metaphyseal striations, and small epiphyses), as well as moderate to severe intellectual disability and facial dysmorphism, including prominent forehead, mild synophrys, depressed nasal bridge, prominent bulbous nasal tip and full lips.","definition_xrefs":["Orphanet:168454"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"},{"relation_name":"is_a","term_name":"spondyloepimetaphyseal dysplasia","termid":"MONDO:0100510"}],"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":"spondyloepimetaphyseal dysplasia, Genevieve type","secondary_identifiers":["OMIM:610442","MESH:C535785","UMLS:C1864872","DOID:0080576","GARD:10057","MEDGEN:355314","icd11.foundation:1383217537"],"synonyms":[{"name":"Nans deficiency","type":"related"},{"name":"SEMD Genevieve type","type":"related"},{"name":"SEMD, Genevieve type","type":"related"},{"name":"SEMD, Geneviève type","type":"exact"},{"name":"SEMDG","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia Genevieve type","type":"related"},{"name":"spondyloepimetaphyseal dysplasia, Camera-Genevieve type","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia, Genevieve type","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia, Geneviève type","type":"related"}],"termid":"MONDO:0012495","xrefs":{"Monarch":{"xref_id":"0012495"}}}


id: GO:0050708
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the controlled release of a protein from a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein transport","termid":"GO:0051223"},{"relation_name":"is_a","term_name":"regulation of secretion by cell","termid":"GO:1903530"},{"relation_name":"regulates","term_name":"protein secretion","termid":"GO:0009306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of protein secretion","termid":"GO:0050708"}


id: PBO:0052429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kizuna centrosomal protein","termid":"PBO:0052429"}


id: GO:1901437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of toluene metabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"toluene metabolic process","termid":"GO:0018970"}],"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 toluene metabolic process","synonyms":[{"name":"regulation of methylbenzene metabolic process","type":"exact"},{"name":"regulation of methylbenzene metabolism","type":"exact"},{"name":"regulation of toluene metabolism","type":"exact"}],"termid":"GO:1901437"}


id: MONDO:0060491
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  {"annotated_genes":["SJAG_02233"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86248],"is_not":false,"summary":null,"term":"MONDO:0060491"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02233":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with involuntary movements","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617493","UMLS:C4479569","GARD:16232","DOID:0112276","MEDGEN:1374697"],"synonyms":[{"name":"NEDIM","type":"related"},{"name":"neurodevelopmental disorder with involuntary movements","type":"exact"}],"termid":"MONDO:0060491","terms_by_termid":{"MONDO:0060491":null},"xrefs":{"Monarch":{"xref_id":"0060491"}}}


id: PBO:0114317
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptional coactivator for ribosomal proteins via TOR signaling pathway Crf1Ifh1","termid":"PBO:0114317"}


id: PBO:0069082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 329, pseudogene","termid":"PBO:0069082"}


id: PBO:0091384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi Ca(2+)/H(+) antiporter Gdt2","termid":"PBO:0091384"}


id: PBO:0113038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Centromeric histone H3-like protein; associates with promoters, accessible chromatin and RNAPII-bound regions; centromeric association promotes kinetochore assembly and Sgo1p association with CEN chromatin; Ipl1p-dependent phosphorylation destabilizes defective kinetochores promoting biorientation; phosphorylation by Cdc7p maintains Cse4p at kinetochores and promotes chromosome segregation; R37 methylation regulates kinetochore function and chromosome segregation; complements human homolog CENPA","termid":"PBO:0113038"}


id: PR:P22193
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cell cycle checkpoint protein RAD1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02073","PANTHER:PTHR10870:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA damage checkpoint control protein rad1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1952.07","secondary_identifiers":["UniProtKB:P22193"],"synonyms":[{"name":"Spom972h-RAD1","type":"exact"}],"termid":"PR:P22193"}


id: GO:0047254
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one + UDP-D-glucose = 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one 2-D-glucoside + UDP.","definition_xrefs":["EC:2.4.1.202"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016757","GO:0003824"],"is_obsolete":false,"name":"2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one 2-D-glucosyltransferase activity","secondary_identifiers":["MetaCyc:RXN-7022","RHEA:15541"],"synonyms":[{"name":"UDP-glucose:2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one 2-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one 2-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one 2-glucosyltransferase activity","type":"related"}],"termid":"GO:0047254"}


id: GO:0042823
data:
  {"annotated_genes":["SJAG_00252","SJAG_00707","SJAG_00283","SJAG_01881","SJAG_00691","SJAG_01383"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63777,87239,94997],"is_not":false,"summary":null,"term":"GO:0042823"},{"annotations":[92325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036001"},{"annotations":[99188,115140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009443"},{"annotations":[111277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010144"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of pyridoxal phosphate, pyridoxal phosphorylated at the hydroxymethyl group of C-5, the active form of vitamin B6.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin B6 biosynthetic process","termid":"GO:0042819"},{"relation_name":"is_a","term_name":"pyridoxal phosphate metabolic process","termid":"GO:0042822"},{"relation_name":"is_a","term_name":"aldehyde biosynthetic process","termid":"GO:0046184"},{"relation_name":"is_a","term_name":"organophosphate biosynthetic process","termid":"GO:0090407"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00252":null,"SJAG_00283":null,"SJAG_00691":null,"SJAG_00707":null,"SJAG_01383":null,"SJAG_01881":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006766"],"is_obsolete":false,"name":"pyridoxal phosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["MetaCyc:PWY0-845"],"synonyms":[{"name":"active vitamin B6 biosynthesis","type":"exact"},{"name":"active vitamin B6 biosynthetic process","type":"exact"},{"name":"pyridoxal phosphate anabolism","type":"exact"},{"name":"pyridoxal phosphate biosynthesis","type":"exact"},{"name":"pyridoxal phosphate formation","type":"exact"},{"name":"pyridoxal phosphate synthesis","type":"exact"}],"termid":"GO:0042823","terms_by_termid":{"GO:0009443":null,"GO:0010144":null,"GO:0036001":null,"GO:0042823":null}}


id: PBO:0048840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine N-methyltransferase","termid":"PBO:0048840"}


id: FYPO:0002420
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce cell that has an abnormal shape and undergoes a single round of cell division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, single cell division","termid":"FYPO:0002280"},{"relation_name":"is_a","term_name":"inviable vegetative cell with abnormal cell shape","termid":"FYPO:0002451"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000004","FYPO:0001320","FYPO:0000005","FYPO:0000002"],"is_obsolete":false,"name":"inviable after spore germination, single cell division, abnormal cell shape","synonyms":[{"name":"inviable following spore germination, single cell division, abnormal cell shape","type":"exact"},{"name":"inviable germinated spore, single cell division, abnormal cell shape","type":"exact"},{"name":"lethal after spore germination, single cell division, abnormal cell shape","type":"exact"}],"termid":"FYPO:0002420"}


id: MONDO:1010992
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hydrocephalus that occurs in sheep.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrocephalus, non-human animal","termid":"MONDO:1010233"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrocephalus, sheep","secondary_identifiers":["OMIA:000487-9940"],"termid":"MONDO:1010992","xrefs":{"Monarch":{"xref_id":"1010992"}}}


id: GO:0021755
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which neuroblasts acquire specialized structural and/or functional features that characterize the mature eurydendroid cell. Differentiation includes the processes involved in commitment of a neuroblast to a eurydendroid cell fate. A eurydendroid cell is an efferent neuron found in the cerebellar cortex of teleosts.","definition_xrefs":["GO_REF:0000021","GOC:jid","PMID:15892096","GOC:dgh","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation in hindbrain","termid":"GO:0021533"},{"relation_name":"is_a","term_name":"central nervous system neuron differentiation","termid":"GO:0021953"},{"relation_name":"part_of","term_name":"cerebellar cortex formation","termid":"GO:0021697"}],"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":"eurydendroid cell differentiation","termid":"GO:0021755"}


id: PBO:0078744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase 6 non-catalytic subunit","termid":"PBO:0078744"}


id: PBO:0042498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 18","termid":"PBO:0042498"}


id: MONDO:0009547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Macrosomia-microphthalmia-cleft palate syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by early macrosomia, bilateral severe microphthalmia and a protuberant abdomen with hepatomegaly. Additional reported features include brachycephaly, large fontanelles, prominent forehead, upturned nose and median cleft palate. Cyanotic apneic spells and overwhelming infection lead to death within the first 6 months of life. There have been no further descriptions in the literature since 1989.","definition_xrefs":["Orphanet:2432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macrosomia-microphthalmia-cleft palate syndrome","secondary_identifiers":["GARD:177","MEDGEN:340874","OMIM:248110","UMLS:C1855467","MESH:C537830"],"synonyms":[{"name":"Teebi Al-Saleh Hassoon syndrome","type":"related"},{"name":"Teebi-Al Saleh-Hassoon syndrome","type":"exact"},{"name":"macrosomia microphthalmia cleft palate","type":"related"},{"name":"macrosomia with lethal microphthalmia","type":"related"},{"name":"macrosomia with microphthalmia, lethal","type":"related"}],"termid":"MONDO:0009547","xrefs":{"Monarch":{"xref_id":"0009547"}}}


id: MONDO:0010429
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the SYP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 96","secondary_identifiers":["OMIM:300802","GARD:22685","UMLS:C3275408","MEDGEN:477039","DOID:0112035"],"synonyms":[{"name":"MRX96","type":"related"},{"name":"SYP non-syndromic X-linked intellectual disability","type":"exact"},{"name":"intellectual developmental disorder, X-linked 96, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked 96","type":"exact"},{"name":"intellectual disability, X-linked type 96","type":"exact"},{"name":"mental retardation, X-linked 96","type":"related"},{"name":"mental retardation, X-linked type 96","type":"exact"},{"name":"non-syndromic X-linked intellectual disability caused by mutation in SYP","type":"exact"}],"termid":"MONDO:0010429","xrefs":{"Monarch":{"xref_id":"0010429"}}}


id: PBO:0060093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 40","termid":"PBO:0060093"}


id: PBO:0034468
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_gene_conversion_during_vegetative_growth","termid":"PBO:0034468"}


id: PBO:0044601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DCAF8 divergent transcript","termid":"PBO:0044601"}


id: PBO:0003636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,2-mannosyltransferase Omh5 (predicted)","termid":"PBO:0003636"}


id: PBO:0077451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM183A pseudogene 1","termid":"PBO:0077451"}


id: MONDO:0017749
data:
  {"annotated_genes":["SJAG_06514","SJAG_03054","SJAG_03158","SJAG_04231","SJAG_00964","SJAG_04697","SJAG_01071","SJAG_05219","SJAG_03723","SJAG_02211","SJAG_00978","SJAG_03153","SJAG_02539","SJAG_00041","SJAG_02903","SJAG_00578","SJAG_01960","SJAG_00831","SJAG_04954"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012637"},{"annotations":[85719],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013281"},{"annotations":[86560],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013325"},{"annotations":[85984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013810"},{"annotations":[86465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012635"},{"annotations":[85958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012123"},{"annotations":[86414],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054559"},{"annotations":[84986,84985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009134"},{"annotations":[84818],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014023"},{"annotations":[84645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014647"},{"annotations":[85216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012556"},{"annotations":[84690],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013049"},{"annotations":[85940,85939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014353"},{"annotations":[85145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009953"},{"annotations":[84778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033556"},{"annotations":[86450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010478"},{"annotations":[86599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012885"},{"annotations":[85314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014790"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00041":null,"SJAG_00578":null,"SJAG_00831":null,"SJAG_00964":null,"SJAG_00978":null,"SJAG_01071":null,"SJAG_01960":null,"SJAG_02211":null,"SJAG_02539":null,"SJAG_02903":null,"SJAG_03054":null,"SJAG_03153":null,"SJAG_03158":null,"SJAG_03723":null,"SJAG_04231":null,"SJAG_04697":null,"SJAG_04954":null,"SJAG_05219":null,"SJAG_06514":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"disorder of multiple glycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:684473574","Orphanet:309526","GARD:21343","MEDGEN:1843364","UMLS:C5681039"],"termid":"MONDO:0017749","terms_by_termid":{"MONDO:0009134":null,"MONDO:0009953":null,"MONDO:0010478":null,"MONDO:0012123":null,"MONDO:0012556":null,"MONDO:0012635":null,"MONDO:0012637":null,"MONDO:0012885":null,"MONDO:0013049":null,"MONDO:0013281":null,"MONDO:0013325":null,"MONDO:0013810":null,"MONDO:0014023":null,"MONDO:0014353":null,"MONDO:0014647":null,"MONDO:0014790":null,"MONDO:0033556":null,"MONDO:0054559":null},"xrefs":{"Monarch":{"xref_id":"0017749"}}}


id: PBO:0086618
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; green fluorescent protein (GFP)-fusion protein localizes to the cell periphery","termid":"PBO:0086618"}


id: GO:0045559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of TRAIL-R2 (TNF-related apoptosis inducing ligand receptor 2), which engages a caspase-dependent apoptotic pathway and mediates apoptosis via the intracellular adaptor molecule FADD/MORT1.","definition_xrefs":["PMID:9311998","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete TRAIL receptor 2 biosynthetic process (obsolete GO:0045559)","synonyms":[{"name":"TRAIL receptor 2 anabolism","type":"exact"},{"name":"TRAIL receptor 2 biosynthesis","type":"exact"},{"name":"TRAIL receptor 2 formation","type":"exact"},{"name":"TRAIL receptor 2 synthesis","type":"exact"},{"name":"tumor necrosis factor receptor superfamily member 10B biosynthetic process","type":"exact"}],"termid":"GO:0045559"}


id: PBO:0060164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-RNR2 like 12 (pseudogene)","termid":"PBO:0060164"}


id: MONDO:0031084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"amelogenesis imperfecta","termid":"MONDO:0019507"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amelogenesis imperfecta, IIa 1K","secondary_identifiers":["OMIM:620104","MEDGEN:1824019","UMLS:C5774246","DOID:0060945"],"synonyms":[{"name":"AI1K","type":"exact"},{"name":"amelogenesis imperfecta, IIa 1K","type":"exact"},{"name":"amelogenesis imperfecta, hypoplastic IIa 1K","type":"exact"}],"termid":"MONDO:0031084","xrefs":{"Monarch":{"xref_id":"0031084"}}}


id: SO:0000243
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Sequence element that recruits a ribosomal subunit to internal mRNA for translation initiation.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribosome_entry_site","termid":"SO:0000139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"internal_ribosome_entry_site","secondary_identifiers":["http://en.wikipedia.org/wiki/Internal_ribosome_entry_site"],"synonyms":[{"name":"IRES","type":"exact"},{"name":"internal ribosomal entry sequence","type":"exact"},{"name":"internal ribosomal entry site","type":"exact"},{"name":"internal ribosome entry sequence","type":"related"},{"name":"internal ribosome entry site","type":"exact"}],"termid":"SO:0000243"}


id: PATO:0000886
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000886 absolute litter size value (obsolete PATO:0000886)","termid":"PATO:0000886"}


id: PBO:0004296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial peptidyl-tRNA hydrolase Pth1 (predicted)","termid":"PBO:0004296"}


id: PBO:0086306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with homology to human PDCD5; PDCD5 is involved in programmed cell death; N-terminal region forms a conserved triple-helix bundle structure; overproduction suppresses lethality due to expression of the dominant PET9 allele AAC2-A128P; overexpression promotes H2O2-induced apoptosis; YMR074C is not an essential gene; protein abundance increases in response to DNA replication stress","termid":"PBO:0086306"}


id: PBO:0004544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore associated protein Thp1-Sac3 complex subunit (predicted)","termid":"PBO:0004544"}


id: PBO:0085330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatidylinositol transfer protein; has a potential role in regulating lipid and fatty acid metabolism under heme-depleted conditions; interacts specifically with thioredoxin peroxidase; may have a role in oxidative stress resistance; protein abundance increases in response to DNA replication stress","termid":"PBO:0085330"}


id: MONDO:0004337
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paget disease involving the perianal skin.","definition_xrefs":["NCIT:C7476"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anal Paget disease","termid":"MONDO:0002651"},{"relation_name":"is_a","term_name":"cutaneous Paget disease","termid":"MONDO:0002655"},{"relation_name":"is_a","term_name":"anal margin carcinoma","termid":"MONDO:0002941"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093","MONDO:0004335"],"is_obsolete":false,"name":"perianal skin Paget disease","secondary_identifiers":["UMLS:C1332270","MEDGEN:231372","DOID:7708"],"synonyms":[{"name":"Paget disease of the anal margin","type":"exact"},{"name":"Paget's disease of the anal margin","type":"exact"},{"name":"anal margin Paget's disease","type":"exact"},{"name":"perianal skin Paget disease","type":"exact"},{"name":"perianal skin Paget's disease","type":"exact"},{"name":"perianal skin mammary Paget's disease","type":"exact"}],"termid":"MONDO:0004337","xrefs":{"Monarch":{"xref_id":"0004337"}}}


id: PR:O14255
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mannosyl-oligosaccharide glucosidase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01350","PANTHER:PTHR10412:SF1","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":"mannosyl-oligosaccharide glucosidase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6G10.09","secondary_identifiers":["UniProtKB:O14255"],"synonyms":[{"name":"Spom972h-MOGS","type":"exact"},{"name":"processing A-glucosidase I (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14255"}


id: PR:O14161
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cwf21 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14161"],"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":"pre-mRNA-splicing factor cwf21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4A8.09c","synonyms":[{"name":"Spom972h-cwf21","type":"exact"},{"name":"complexed with cdc5 protein 21 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14161"}


id: MONDO:0001147
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital abnormality in which the meninges protrude through a defect in the spinal column or the cranium.","definition_xrefs":["NCIT:C105595"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spina bifida","termid":"MONDO:0008449"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"}],"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":"meningocele","secondary_identifiers":["MESH:D008588","SCTID:171131006","UMLS:C0025299","MEDGEN:44356","DOID:1088","Orphanet:93968","HP:0002435","NCIT:C101209"],"synonyms":[{"name":"central nervous system meningocele","type":"exact"},{"name":"meningocele","type":"exact"},{"name":"meningocele (disease)","type":"exact"},{"name":"spinal meningocele","type":"narrow"}],"termid":"MONDO:0001147","xrefs":{"Monarch":{"xref_id":"0001147"}}}


id: MONDO:0054770
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Orofaciodigital syndrome 18 (OFD18) is characterized by short stature, brachymesophalangy, pre- and postaxial polysyndactyly, and stocky femoral necks, as well as oral anomalies and dysmorphic facial features.","definition_xrefs":["OMIM:617927"],"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 18","secondary_identifiers":["DOID:0060961","Orphanet:508501","MEDGEN:1799326","UMLS:C5567903"],"synonyms":[{"name":"OFD18","type":"exact"},{"name":"Ofds 18","type":"exact"},{"name":"oral-facial-digital syndrome type 18","type":"exact"},{"name":"oral-facial-digital syndrome with short stature and brachymesophalangy","type":"exact"},{"name":"orofaciodigital syndrome XVIII","type":"exact"},{"name":"orofaciodigital syndrome type 18","type":"exact"}],"termid":"MONDO:0054770","xrefs":{"Monarch":{"xref_id":"0054770"}}}


id: FYPO:0000571
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the rate, or speed, of mating projection assembly is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal shmoo formation","termid":"FYPO:0000568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000301","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased rate of shmoo formation","synonyms":[{"name":"decreased rate of conjugation tube formation","type":"exact"},{"name":"decreased rate of mating projection assembly","type":"exact"},{"name":"decreased rate of mating projection formation","type":"exact"},{"name":"decreased rate of shmoo assembly","type":"exact"},{"name":"reduced rate of shmoo formation","type":"exact"},{"name":"shmoo formation: decreased rate","type":"related"}],"termid":"FYPO:0000571"}


id: FYPO:0004667
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cohesion between sister chromatids is normal (i.e. indistinguishable from wild type) at the centromeric regions during meiosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal meiotic sister chromatid cohesion","termid":"FYPO:0002094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal meiotic sister chromatid cohesion at centromere","synonyms":[{"name":"normal meiotic sister chromatid cohesion, centromeric","type":"exact"},{"name":"normal sister chromatid cohesion at centromere during meiosis","type":"exact"}],"termid":"FYPO:0004667"}


id: GO:0003073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that modulates the force with which blood travels through the systemic arterial circulatory system. The process is controlled by a balance of processes that increase pressure and decrease pressure.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of blood pressure","termid":"GO:0008217"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of systemic arterial blood pressure","termid":"GO:0003073"}


id: PR:O14073
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPACUNK4.08 gene.","definition_xrefs":["UniProtKB:O14073","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":"dipeptidyl aminopeptidase C2E11.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPACUNK4.08","synonyms":[{"name":"Spom972h-SPACUNK4.08","type":"exact"}],"termid":"PR:O14073"}


id: PBO:0084163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Highly conserved iron-sulfur cluster binding protein; localized in the cytoplasm; forms a complex with Nbp35p that is involved in iron-sulfur protein assembly in the cytosol","termid":"PBO:0084163"}


id: PBO:0069557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 829, pseudogene","termid":"PBO:0069557"}


id: GO:0048567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the ectodermal digestive tract are generated and organized. The ectodermal digestive tract includes those portions of the digestive tract that are derived from ectoderm.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal digestive tract development","termid":"GO:0007439"},{"relation_name":"part_of","term_name":"digestive tract morphogenesis","termid":"GO:0048546"}],"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":"ectodermal digestive tract morphogenesis","synonyms":[{"name":"ectodermal gut morphogenesis","type":"related"}],"termid":"GO:0048567"}


id: MONDO:0030756
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Stuve-Wiedemann syndrome","termid":"MONDO:0031280"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Stuve-Wiedemann syndrome 2","secondary_identifiers":["OMIM:619751","UMLS:C5676919","MEDGEN:1805977"],"synonyms":[{"name":"STWS2","type":"exact"},{"name":"Stuve-Wiedemann syndrome 2","type":"exact"}],"termid":"MONDO:0030756","xrefs":{"Monarch":{"xref_id":"0030756"}}}


id: MONDO:0100055
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intraosseous spindle cell rhabdomyosarcoma characterized by the fusion of the EWSR1 or FUS gene with the TFCP2 gene, or the MEIS1 gene with the NCOA2 gene.","definition_xrefs":["NCIT:C178236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle cell rhabdomyosarcoma","termid":"MONDO:0002581"}],"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":"intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements","secondary_identifiers":["UMLS:C5554888","MEDGEN:1791329"],"synonyms":[{"name":"intraosseous rhabdomyosarcoma defined by FUS-TFCP2 fusion","type":"related"},{"name":"intraosseous rhabdomyosarcoma with FUS-TFCP2 fusion","type":"narrow"}],"termid":"MONDO:0100055","xrefs":{"Monarch":{"xref_id":"0100055"}}}


id: PBO:0058175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4470","termid":"PBO:0058175"}


id: MONDO:0003053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the choroid plexus.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choroid plexus cancer","termid":"MONDO:0002681"},{"relation_name":"is_a","term_name":"intraventricular meningioma","termid":"MONDO:0002772"}],"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":"choroid plexus meningioma","secondary_identifiers":["DOID:4584","MEDGEN:98458","UMLS:C0431118","NCIT:C4719"],"synonyms":[{"name":"choroid meningioma (morphologic abnormality)","type":"exact"},{"name":"choroid plexus meningioma","type":"exact"},{"name":"choroid plexus meningioma (disease)","type":"exact"},{"name":"meningioma (disease) of choroid plexus","type":"exact"},{"name":"meningioma of choroid plexus","type":"related"},{"name":"meningioma of the choroid plexus","type":"exact"}],"termid":"MONDO:0003053","xrefs":{"Monarch":{"xref_id":"0003053"}}}


id: PBO:0071768
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein lateral stalk subunit P2 pseudogene 1","termid":"PBO:0071768"}


id: MONDO:0970944
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Leigh syndrome, mitochondrial","secondary_identifiers":["OMIM:500017"],"termid":"MONDO:0970944","xrefs":{"Monarch":{"xref_id":"0970944"}}}


id: MONDO:0009741
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroblastoma, susceptibility to, 1","secondary_identifiers":["OMIM:256700","MEDGEN:412713","UMLS:C2749485"],"synonyms":[{"name":"neuroblastoma, susceptibility to","type":"broad"},{"name":"neuroblastoma, susceptibility to, 1, autosomal dominant, somatic mutation","type":"exact"},{"name":"susceptibility to neuroblastoma","type":"broad"}],"termid":"MONDO:0009741","xrefs":{"Monarch":{"xref_id":"0009741"}}}


id: FYPO:0005722
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a mitotic spindle assembles and begins to elongate, but becomes curved during anaphase B and eventually collapses. The spindle pole bodies separate, but often become spatially closer together as the spindle elongates and curves.","definition_xrefs":["PMID:15147872","PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic spindle collapse","termid":"FYPO:0006475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000641","FYPO:0000002","FYPO:0000631","FYPO:0000337"],"is_obsolete":false,"name":"mitotic spindle collapse during anaphase B elongation","synonyms":[{"name":"broken mitotic spindle during anaphase B elongation","type":"related"},{"name":"mitotic spindle breakage during anaphase B elongation","type":"exact"},{"name":"mitotic spindle collapse during elongation during anaphase B","type":"exact"},{"name":"mitotic spindle curvature and collapse during anaphase B","type":"exact"}],"termid":"FYPO:0005722"}


id: GO:0015750
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which pentose is transported across a lipid bilayer, from one side of a membrane to the other. A pentose is any aldose with a chain of five carbon atoms in the molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide transmembrane transport","termid":"GO:0015749"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"pentose transmembrane transport","synonyms":[{"name":"pentose transport","type":"related"}],"termid":"GO:0015750"}


id: PATO:0002068
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial pattern inhering in a bearer by virtue of the bearer's exhibiting a layered configuration.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stratification","termid":"PATO:0002067"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stratified","termid":"PATO:0002068"}


id: PBO:0088596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor Moc3","termid":"PBO:0088596"}


id: PBO:0091378
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds with high affinity to mammalian-type 5'-TTAGGG-3' telomeric repeats, and with very low affinity to less stringently conserved S. pombe telomeric repeats","termid":"PBO:0091378"}


id: PBO:0004740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear RNA U3B","termid":"PBO:0004740"}


id: GO:0099500
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Fusion of the membrane of a vesicle with the plasma membrane, thereby releasing its contents into the extracellular space.","definition_xrefs":["ISBN:0071120009","PMID:18618940","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle fusion","termid":"GO:0006906"},{"relation_name":"is_a","term_name":"exocytic process","termid":"GO:0140029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0008150","GO:0061024"],"is_obsolete":false,"name":"vesicle fusion to plasma membrane","termid":"GO:0099500"}


id: PBO:0082744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the RSC chromatin remodeling complex; interacts with Rsc3p, Rsc30p, Ldb7p, and Htl1p to form a module important for a broad range of RSC functions","termid":"PBO:0082744"}


id: PBO:0089235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial nuclease Lcl3, implicated in DNA repair","termid":"PBO:0089235"}


id: PBO:0075224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 2 pseudogene 1","termid":"PBO:0075224"}


id: PBO:0035997
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_methylation_at_centromere_central_core_during_vegetative_growth","termid":"PBO:0035997"}


id: PBO:0056627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 8","termid":"PBO:0056627"}


id: GO:0072011
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the glomerular endothelium over time, from its formation to the mature structure. The glomerular endothelium is an epithelial tissue that covers the internal surfaces of the glomerulus.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelium development","termid":"GO:0003158"},{"relation_name":"is_a","term_name":"glomerular epithelium development","termid":"GO:0072010"},{"relation_name":"part_of","term_name":"glomerulus vasculature development","termid":"GO:0072012"}],"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":"glomerular endothelium development","termid":"GO:0072011"}


id: GO:0099111
data:
  {"annotated_genes":["SJAG_00368","SJAG_02731","SJAG_03835","SJAG_04143","SJAG_01662","SJAG_04387","SJAG_01546","SJAG_02737","SJAG_05266","SJAG_00332","SJAG_02561","SJAG_01211","SJAG_02431","SJAG_04003","SJAG_01370","SJAG_02509","SJAG_04597","SJAG_01775","SJAG_00851","SJAG_04001","SJAG_03540","SJAG_01371","SJAG_03673","SJAG_01863","SJAG_01613","SJAG_05185","SJAG_03073","SJAG_00140","SJAG_01297","SJAG_05220","SJAG_05319","SJAG_00113","SJAG_02286","SJAG_00397","SJAG_00918","SJAG_02336","SJAG_01224","SJAG_03437","SJAG_02761","SJAG_02045"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97077,94708,87272,100920,116386,113387,90895,110501,102741,100219,91351,90505,102450,110676,110854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030989"},{"annotations":[100921,110678,106056],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032118"},{"annotations":[116390,106895,100932,113389,109072,111580,103497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098863"},{"annotations":[98734,97151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090561"},{"annotations":[87276,94710,97079,98735,90897],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000743"},{"annotations":[93920],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1902854"},{"annotations":[103235],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099117"},{"annotations":[103387,118102,107726,99880],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140210"},{"annotations":[100012,88655,116360,90493,109353,106970,113540,108343,89259,96276,98132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990976"},{"annotations":[90659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010970"}]},"cv_name":"biological_process","definition":"A microtubule-based process that results in the transport of organelles, other microtubules, or other cellular components. Examples include motor-driven movement along microtubules and movement driven by polymerization or depolymerization of microtubules.","definition_xrefs":["GOC:cjm","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"}],"gene_count":40,"genes_by_uniquename":{"SJAG_00113":null,"SJAG_00140":null,"SJAG_00332":null,"SJAG_00368":null,"SJAG_00397":null,"SJAG_00851":null,"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01297":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01546":null,"SJAG_01613":null,"SJAG_01662":null,"SJAG_01775":null,"SJAG_01863":null,"SJAG_02045":null,"SJAG_02286":null,"SJAG_02336":null,"SJAG_02431":null,"SJAG_02509":null,"SJAG_02561":null,"SJAG_02731":null,"SJAG_02737":null,"SJAG_02761":null,"SJAG_03073":null,"SJAG_03437":null,"SJAG_03540":null,"SJAG_03673":null,"SJAG_03835":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04143":null,"SJAG_04387":null,"SJAG_04597":null,"SJAG_05185":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:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"microtubule-based transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0099111","terms_by_termid":{"GO:0000743":null,"GO:0010970":null,"GO:0030989":null,"GO:0032118":null,"GO:0090561":null,"GO:0098863":null,"GO:0099117":null,"GO:0140210":null,"GO:1902854":null,"GO:1990976":null}}


id: GO:0075270
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of aecium development, a process in which a cuplike structure containing chains of aeciospores is formed.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of spore-bearing organ development","termid":"GO:0075262"},{"relation_name":"is_a","term_name":"regulation of aecium development","termid":"GO:0075268"},{"relation_name":"negatively_regulates","term_name":"aecium development","termid":"GO:0075267"}],"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 aecium development","termid":"GO:0075270"}


id: PBO:0044665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dicarbonyl and L-xylulose reductase","termid":"PBO:0044665"}


id: GO:0045010
data:
  {"annotated_genes":["SJAG_01964","SJAG_01384","SJAG_02228","SJAG_03455","SJAG_01732","SJAG_02245","SJAG_03086","SJAG_02075","SJAG_04479","SJAG_04100","SJAG_01268","SJAG_04624"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88880],"is_not":false,"summary":null,"term":"GO:0045010"},{"annotations":[87666,99360,102229,102797,90189,104634,106629,97418,98340,99183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034314"},{"annotations":[90387],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0034316"}]},"cv_name":"biological_process","definition":"The initial step in the formation of an actin filament, in which actin monomers combine to form a new filament. Nucleation is slow relative to the subsequent addition of more monomers to extend the filament.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament organization","termid":"GO:0007015"}],"gene_count":12,"genes_by_uniquename":{"SJAG_01268":null,"SJAG_01384":null,"SJAG_01732":null,"SJAG_01964":null,"SJAG_02075":null,"SJAG_02228":null,"SJAG_02245":null,"SJAG_03086":null,"SJAG_03455":null,"SJAG_04100":null,"SJAG_04479":null,"SJAG_04624":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0030036"],"is_obsolete":false,"name":"actin nucleation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"actin filament nucleation","type":"exact"}],"termid":"GO:0045010","terms_by_termid":{"GO:0034314":null,"GO:0034316":null,"GO:0045010":null}}


id: FYPO:0005016
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 posttranscriptional addition of acetyl groups to residues in an 18S rRNA molecule is abolished.","definition_xrefs":["PMID:25402480","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal rRNA modification","termid":"FYPO:0005015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0006551","FYPO:0000002","FYPO:0001320","FYPO:0000294"],"is_obsolete":false,"name":"abolished 18S rRNA acetylation","synonyms":[{"name":"18S rRNA acetylation abolished","type":"exact"},{"name":"abolished 18S rRNA acetylation at C1297 and C1815","type":"narrow"},{"name":"abolished 18S rRNA acetylation during mitotic cell cycle","type":"related"},{"name":"abolished 18S rRNA acetylation during vegetative growth","type":"exact"},{"name":"abolished 18S rRNA acetylation on C1297 and C1815","type":"exact"},{"name":"abolished 18s rRNA cytidine (1297 and 1815) acetylation","type":"narrow"}],"termid":"FYPO:0005016"}


id: PBO:0064570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"popeye domain containing 2","termid":"PBO:0064570"}


id: PBO:0069833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1119, pseudogene","termid":"PBO:0069833"}


id: PBO:0000977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF3j (p35)","termid":"PBO:0000977"}


id: FYECO:0000450
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which miconazole was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ miconazole","termid":"FYECO:0000450"}


id: MONDO:0000990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of subendocardial myocardial infarction.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"subendocardial myocardial infarction","termid":"MONDO:0003674"},{"relation_name":"is_a","term_name":"acute myocardial infarction","termid":"MONDO:0004781"}],"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":"acute subendocardial myocardial infarction","secondary_identifiers":["ICD9:410.71","UMLS:C0264710","ICD9:410.7","SCTID:70422006","MEDGEN:538778","ICD9:410.72","DOID:10266","ICD9:410.70"],"synonyms":[{"name":"acute nontransmural infarction","type":"related"},{"name":"acute subendocardial infarction","type":"exact"},{"name":"subendocardial infarction acute myocardial infarction","type":"related"},{"name":"subendocardial myocardial infarction, acute","type":"exact"}],"termid":"MONDO:0000990","xrefs":{"Monarch":{"xref_id":"0000990"}}}


id: GO:0007409
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"De novo generation of a long process of a neuron, including the terminal branched region. Refers to the morphogenesis or creation of shape or form of the developing axon, which carries efferent (outgoing) action potentials from the cell body towards target cells.","definition_xrefs":["ISBN:0198506732","GOC:jid","GOC:dph","GOC:pg","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection morphogenesis","termid":"GO:0048812"},{"relation_name":"part_of","term_name":"cell morphogenesis involved in neuron differentiation","termid":"GO:0048667"},{"relation_name":"part_of","term_name":"axon development","termid":"GO:0061564"}],"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":"axonogenesis","secondary_identifiers":["GO:0007410"],"synonyms":[{"name":"axon growth","type":"narrow"},{"name":"axon morphogenesis","type":"exact"},{"name":"neuron long process generation","type":"exact"}],"termid":"GO:0007409"}


id: PBO:0001887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribomal-ubiquitin fusion protein Ubi5 (predicted)","termid":"PBO:0001887"}


id: PBO:0085254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peripheral membrane protein of the plasma membrane; interacts with Mid2p; regulates the cell integrity pathway mediated by Pkc1p and Slt2p; the authentic protein is detected in a phosphorylated state in highly purified mitochondria","termid":"PBO:0085254"}


id: GO:1903804
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of glycine from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GO_REF:0000075","GOC:TermGenie","PMID:23895341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycine transport","termid":"GO:0015816"},{"relation_name":"is_a","term_name":"amino acid import across plasma membrane","termid":"GO:0089718"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"glycine import across plasma membrane","secondary_identifiers":["GO:0036233"],"synonyms":[{"name":"glycine import","type":"broad"},{"name":"glycine import into cell","type":"exact"}],"termid":"GO:1903804"}


id: GO:0010188
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 microbial phytotoxin stimulus. A microbial phytotoxin is a chemical substance produced by microbes which is toxic to plants.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to toxic substance","termid":"GO:0009636"}],"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 microbial phytotoxin","termid":"GO:0010188"}


id: RO:HOM0000011
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Historical homology that involves genes that diverged after a duplication event.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_historical_homology_relationship_with","termid":"RO:HOM0000007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_paralogy_relationship_with","synonyms":[{"name":"paralogous to","type":"exact"}],"termid":"RO:HOM0000011"}


id: PR:O59759
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1020.05 gene.","definition_xrefs":["UniProtKB:O59759","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 C1020.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1020.05","synonyms":[{"name":"Spom972h-SPCC1020.05","type":"exact"}],"termid":"PR:O59759"}


id: PBO:0044445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily F member 23, pseudogene","termid":"PBO:0044445"}


id: MONDO:0100280
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoplasmacytic lymphoma","termid":"MONDO:0000432"},{"relation_name":"is_a","term_name":"indolent B-cell non-Hodgkin lymphoma","termid":"MONDO:0017594"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"Waldenstrom macroglobulinemia","secondary_identifiers":["UMLS:C0024419","EFO:0009441","MedDRA:10047801","Orphanet:33226","GARD:7872","OMIMPS:153600","ONCOTREE:WM","MESH:D008258","DOID:0060901","ICD10CM:C88.0","MEDGEN:6174","NCIT:C80307","NORD:1834"],"synonyms":[{"name":"Waldenstroem's macroglobulinemia","type":"related"},{"name":"Waldenstrom macroglobulinemia","type":"exact"},{"name":"Waldenstrom's macroglobulinaemia","type":"related"},{"name":"Waldenstrom's macroglobulinemia","type":"exact"},{"name":"Waldenstrom's syndrome","type":"related"},{"name":"Waldenström Macroglobulinemia","type":"exact"},{"name":"Waldenström macroglobulinemia","type":"exact"},{"name":"lymphoplasmacytic lymphoma with IgM gammopathy","type":"exact"},{"name":"macroglobulinemia of Waldenstrom","type":"related"}],"termid":"MONDO:0100280","xrefs":{"Monarch":{"xref_id":"0100280"}}}


id: PBO:0031722
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_meiotic_recombination","termid":"PBO:0031722"}


id: PBO:0018248
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae SPO13","termid":"PBO:0018248"}


id: MONDO:0006633
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the gallbladder in the absence of gallstones.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholecystitis","termid":"MONDO:0002155"},{"relation_name":"is_a","term_name":"cystitis","termid":"MONDO:0006032"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"acalculous cholecystitis","secondary_identifiers":["MEDGEN:82762","DOID:2828","UMLS:C0267841","MESH:D042101","NCIT:C35578","EFO:1000790","MedDRA:10000347","SCTID:19968009"],"synonyms":[{"name":"acute acalculous cholecystitis","type":"narrow"},{"name":"acute cholecystitis without calculus","type":"exact"},{"name":"cholecystitis without calculus","type":"exact"}],"termid":"MONDO:0006633","xrefs":{"Monarch":{"xref_id":"0006633"}}}


id: MONDO:0012092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary sensory and autonomic neuropathy, type 5 (HSAN5) is characterized by loss of pain perception and impaired temperature sensitivity, in the absence of any other major neurological anomalies.","definition_xrefs":["Orphanet:64752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary sensory and autonomic neuropathy","termid":"MONDO:0015364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"hereditary sensory and autonomic neuropathy type 5","secondary_identifiers":["PMID:14976160","PMID:77656","GARD:12328","OMIM:608654","icd11.foundation:1411011731","UMLS:C0020075","DOID:0070145","MEDGEN:6916","SCTID:128206006"],"synonyms":[{"name":"HSAN 5","type":"related"},{"name":"HSAN V","type":"related"},{"name":"HSAN5","type":"exact"},{"name":"NGF autosomal recessive hereditary sensory and autonomic neuropathy","type":"exact"},{"name":"autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF","type":"exact"},{"name":"congenital insensitivity to pain and thermal analgesia","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type V","type":"exact"},{"name":"insensitivity to pain, congenital","type":"related"},{"name":"neuropathy, hereditary sensory and autonomic, type 5","type":"related"},{"name":"neuropathy, hereditary sensory and autonomic, type V","type":"related"}],"termid":"MONDO:0012092","xrefs":{"Monarch":{"xref_id":"0012092"}}}


id: PBO:0045584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deoxyuridine triphosphatase pseudogene 6","termid":"PBO:0045584"}


id: PBO:0041501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 12 open reading frame 75","termid":"PBO:0041501"}


id: PBO:0047459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ficolin 3","termid":"PBO:0047459"}


id: GO:0015699
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of antimonite into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inorganic anion transmembrane transport","termid":"GO:0098661"}],"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:0006810","GO:0008150","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"antimonite transmembrane transport","synonyms":[{"name":"antimonite transport","type":"broad"}],"termid":"GO:0015699"}


id: GO:0061298
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the vasculature of the retina over time, from its formation to the mature structure.","definition_xrefs":["GOC:dph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vasculature development","termid":"GO:0001944"},{"relation_name":"part_of","term_name":"retina development in camera-type eye","termid":"GO:0060041"}],"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":"retina vasculature development in camera-type eye","synonyms":[{"name":"retinal vasculature development","type":"exact"}],"termid":"GO:0061298"}


id: PBO:0057293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 511","termid":"PBO:0057293"}


id: PBO:0039925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGEF26 antisense RNA 1","termid":"PBO:0039925"}


id: MONDO:0002094
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete conjunctival squamous cell carcinoma (obsolete MONDO:0002094)","termid":"MONDO:0002094","xrefs":{"Monarch":{"xref_id":"0002094"}}}


id: PBO:0039561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 54","termid":"PBO:0039561"}


id: MOD:01331
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-arginine residue to 6x(13)C labeled L-arginine.","definition_xrefs":["PubMed:12716131","OMSSA:136","Unimod:188#R"],"direct_ancestors":[{"relation_name":"is_a","term_name":"6x(13)C labeled residue","termid":"MOD:00544"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C labeled L-arginine","synonyms":[{"name":"13C(6) Silac label","type":"related"},{"name":"Label:13C(6)","type":"related"},{"name":"arg-13c6","type":"exact"}],"termid":"MOD:01331"}


id: PBO:0083938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Galactose permease; required for utilization of galactose; also able to transport glucose","termid":"PBO:0083938"}


id: GO:0032990
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which the anatomical structures of a cell part are generated and organized.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete cell part morphogenesis (obsolete GO:0032990)","termid":"GO:0032990"}


id: MONDO:0014467
data:
  {"annotated_genes":["SJAG_01190"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86405],"is_not":false,"summary":null,"term":"MONDO:0014467"}]},"cv_name":"mondo","definition":"Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the COX6A1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"},{"relation_name":"is_a","term_name":"autosomal recessive intermediate Charcot-Marie-Tooth disease","termid":"MONDO:0017058"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01190":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0006025","MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease recessive intermediate D","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0110203","MEDGEN:1800450","GARD:17723","OMIM:616039","Orphanet:435998","UMLS:C5569027"],"synonyms":[{"name":"CMTRID","type":"exact"},{"name":"COX6A1 Charcot-Marie-Tooth disease","type":"exact"},{"name":"Charcot-Marie-Tooth disease caused by mutation in COX6A1","type":"exact"},{"name":"Charcot-Marie-Tooth disease recessive intermediate type D","type":"exact"},{"name":"Charcot-Marie-Tooth disease, recessive Intermediate type D","type":"exact"},{"name":"Charcot-Marie-Tooth disease, recessive intermediate D","type":"related"},{"name":"RI-CMT type D","type":"exact"},{"name":"autosomal recessive intermediate Charcot-Marie-Tooth disease type D","type":"exact"}],"termid":"MONDO:0014467","terms_by_termid":{"MONDO:0014467":null},"xrefs":{"Monarch":{"xref_id":"0014467"}}}


id: MONDO:0017880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rift Valley fever (RVF), caused by the Rift Valley fever virus (RVFV), is an arbovirus characterized by a usually self-limiting febrile illness but that in some cases can also manifest with thrombosis, vision loss, hemorrhages and/or neurological symptoms.","definition_xrefs":["Orphanet:319251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rift valley fever","secondary_identifiers":["SCTID:402917003","MESH:D012295","DOID:1328","icd11.foundation:854137188","NCIT:C128419","MEDGEN:20589","MedDRA:10039143","ICD10CM:A92.4","GARD:21416","UMLS:C0035613"],"synonyms":[{"name":"RVF","type":"exact"}],"termid":"MONDO:0017880","xrefs":{"Monarch":{"xref_id":"0017880"}}}


id: PBO:0066171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBIS pseudogene 4","termid":"PBO:0066171"}


id: MONDO:0015473
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cryptorchidism-arachnodactyly-intellectual disability syndrome is a rare, multiple congenital anomalies syndrome characterized by psychomotor delay, severe intellectual deficit, severe muscle hypoplasia (with absence of subcutaneous fatty tissue), generalized contractures, craniofacial dysmorphic features (dolichocephaly, esotropia, ears of unequal size, high palate), chest and spinal deformities (i.e. sternum shifted to side, kyphoscoliosis), pulmonary anomalies (unilateral hypoplastic bronchial system), arachnodactyly, and genital abnormalities (cryptorchidism, hypospadias, testicular agenesis). Repeated respiratory tract infections and atelectasis are also associated. There have been no further descriptions in the literature since 1970.","definition_xrefs":["Orphanet:1548"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cryptorchidism-arachnodactyly-intellectual disability syndrome","secondary_identifiers":["GARD:860","MEDGEN:1647147","UMLS:C4707233"],"synonyms":[{"name":"Van Benthem-Driessen-Hanveld syndrome","type":"exact"},{"name":"cryptorchidism arachnodactyly intellectual deficit","type":"related"}],"termid":"MONDO:0015473","xrefs":{"Monarch":{"xref_id":"0015473"}}}


id: MONDO:0017279
data:
  {"annotated_genes":["SJAG_16459","SJAG_02106","SJAG_03866","SJAG_04757","SJAG_00063","SJAG_01229","SJAG_04545","SJAG_04404"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85324,85323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014796"},{"annotations":[85717,85718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011658"},{"annotations":[85332,85333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014233"},{"annotations":[86463,86464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011706"}]},"cv_name":"mondo","definition":"A form of Parkinson disease (PD) characterized by an age of onset between 21-45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints and falls, and other non-motor symptoms. A slow disease progression and a more pronounced response to dopaminergic therapy are also observed in most YOPD forms.","definition_xrefs":["Orphanet:2828"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"primary orthostatic hypotension","termid":"MONDO:0015914"},{"relation_name":"is_a","term_name":"Parkinson disease","termid":"MONDO:0005180"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00063":null,"SJAG_01229":null,"SJAG_02106":null,"SJAG_03866":null,"SJAG_04404":null,"SJAG_04545":null,"SJAG_04757":null,"SJAG_16459":null},"genotype_count":0,"is_obsolete":false,"name":"young-onset Parkinson disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16610","SCTID:715345007","UMLS:C4275179","MEDGEN:907947","DOID:0060894"],"synonyms":[{"name":"YOPD","type":"exact"},{"name":"early-onset Parkinson disease","type":"exact"},{"name":"early-onset Parkinson's disease","type":"related"}],"termid":"MONDO:0017279","terms_by_termid":{"MONDO:0011658":null,"MONDO:0011706":null,"MONDO:0014233":null,"MONDO:0014796":null},"xrefs":{"Monarch":{"xref_id":"0017279"}}}


id: PBO:0050745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family E (Hsp10) member 1 pseudogene 7","termid":"PBO:0050745"}


id: MONDO:0005864
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm affecting the skeletal or smooth muscles. Malignant neoplasms arising from the skeletal muscles are called rhabdomyosarcomas. Malignant neoplasms arising from the smooth muscles are called leiomyosarcomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system cancer","termid":"MONDO:0000637"}],"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":"muscle cancer","secondary_identifiers":["EFO:0007384","NCIT:C4883","MEDGEN:151927","DOID:4045","ICDO:8895/3","ICD9:171.9","SCTID:363495004","UMLS:C0684743"],"synonyms":[{"name":"cancer of muscle structure","type":"exact"},{"name":"malignant muscle neoplasm","type":"exact"},{"name":"malignant muscle structure neoplasm","type":"exact"},{"name":"malignant muscle tumor","type":"exact"},{"name":"malignant muscle tumour","type":"exact"},{"name":"malignant neoplasm of muscle","type":"exact"},{"name":"malignant neoplasm of muscle structure","type":"exact"},{"name":"malignant neoplasm of the muscle","type":"exact"},{"name":"malignant tumor of muscle","type":"exact"},{"name":"malignant tumor of the muscle","type":"exact"},{"name":"malignant tumour of muscle","type":"exact"},{"name":"malignant tumour of the muscle","type":"exact"},{"name":"muscle structure cancer","type":"exact"},{"name":"myosarcoma","type":"exact"}],"termid":"MONDO:0005864","xrefs":{"Monarch":{"xref_id":"0005864"}}}


id: PBO:0027707
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_DNA_polymerase_processivity_factor_activity","termid":"PBO:0027707"}


id: PBO:0083660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endoplasmic reticulum (ER) localized integral membrane protein; may promote secretion of certain hexose transporters, including Gal2p; involved in glucose-dependent repression","termid":"PBO:0083660"}


id: MONDO:0030074
data:
  {"annotated_genes":["SJAG_00321"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84904],"is_not":false,"summary":null,"term":"MONDO:0030074"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00321":null},"genotype_count":0,"is_obsolete":false,"name":"spondylometaphyseal dysplasia with corneal dystrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618961","Orphanet:589435","UMLS:C5394555","DOID:0112303","GARD:18016","MEDGEN:1714019"],"synonyms":[{"name":"SMDCD","type":"exact"},{"name":"SPONDYLOMETAPHYSEAL DYSPLASIA WITH CORNEAL DYSTROPHY","type":"exact"},{"name":"spondylometaphyseal dysplasia with corneal dystrophy","type":"exact"}],"termid":"MONDO:0030074","terms_by_termid":{"MONDO:0030074":null},"xrefs":{"Monarch":{"xref_id":"0030074"}}}


id: GO:0033603
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the regulated release of dopamine.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of dopamine secretion","termid":"GO:0014059"},{"relation_name":"is_a","term_name":"positive regulation of catecholamine secretion","termid":"GO:0033605"},{"relation_name":"positively_regulates","term_name":"dopamine secretion","termid":"GO:0014046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of dopamine secretion","synonyms":[{"name":"activation of dopamine secretion","type":"narrow"},{"name":"stimulation of dopamine secretion","type":"narrow"},{"name":"up regulation of dopamine secretion","type":"exact"},{"name":"up-regulation of dopamine secretion","type":"exact"},{"name":"upregulation of dopamine secretion","type":"exact"}],"termid":"GO:0033603"}


id: MONDO:0009260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"GM1 gangliosidosis type 1 is the severe infantile form of GM1 gangliosidosis with variable neurological and systemic manifestations.","definition_xrefs":["Orphanet:79255"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic dyslipidemia","termid":"MONDO:0015905"},{"relation_name":"is_a","term_name":"GM1 gangliosidosis","termid":"MONDO:0018149"},{"relation_name":"is_a","term_name":"lysosomal storage disease with skeletal involvement","termid":"MONDO:0800088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0002525","MONDO:0005066","MONDO:0005328"],"is_obsolete":false,"name":"GM1 gangliosidosis type 1","secondary_identifiers":["GARD:6479","NANDO:1200067","NANDO:2201196","MONDO:0023211","UMLS:C0268271","MEDGEN:75665","OMIM:230500","DOID:0080502","SCTID:238026007","icd11.foundation:466200180"],"synonyms":[{"name":"Beta galactosidase deficiency type 1","type":"related"},{"name":"Beta-galactosidase-1 deficiency","type":"related"},{"name":"GLB deficiency type 1","type":"related"},{"name":"GM1-gangliosidosis, type 1","type":"related"},{"name":"GM1-gangliosidosis, type I","type":"related"},{"name":"GM1-gangliosidosis, type I, with Cardiac involvement","type":"related"},{"name":"Glb1 deficiency","type":"related"},{"name":"Norman-Landing disease","type":"exact"},{"name":"gangliosidosis generalised GM1 infantile form","type":"related"},{"name":"gangliosidosis generalised GM1 type 1","type":"related"},{"name":"gangliosidosis generalized GM1 infantile form","type":"related"},{"name":"gangliosidosis generalized GM1 type 1","type":"related"},{"name":"gangliosidosis, generalised GM1, infantile form","type":"related"},{"name":"gangliosidosis, generalised GM1, type 1","type":"related"},{"name":"gangliosidosis, generalised GM1, type I, with Cardiac involvement","type":"related"},{"name":"gangliosidosis, generalized GM1, infantile form","type":"related"},{"name":"gangliosidosis, generalized GM1, type 1","type":"related"},{"name":"gangliosidosis, generalized GM1, type I, with Cardiac involvement","type":"related"},{"name":"infantile GM1 gangliosidosis","type":"exact"}],"termid":"MONDO:0009260","xrefs":{"Monarch":{"xref_id":"0009260"}}}


id: PBO:0068095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 402","termid":"PBO:0068095"}


id: PBO:0111819
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PQ loop","termid":"PBO:0111819"}


id: PR:O74810
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ubiquitin-conjugating enzyme E2 K that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03517","PANTHER:PTHR24067:SF28"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-conjugating enzyme E2 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2D10.20","secondary_identifiers":["UniProtKB:O74810"],"synonyms":[{"name":"E2 ubiquitin-conjugating enzyme 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-UBE2K","type":"exact"},{"name":"ubiquitin carrier protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-protein ligase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74810"}


id: FYECO:0000423
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which ciclopirox olamine was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ ciclopirox olamine","synonyms":[{"name":"+ ciclopirox olamine","type":"exact"}],"termid":"FYECO:0000423"}


id: PBO:0080780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XK related, Y-linked, pseudogene","termid":"PBO:0080780"}


id: MONDO:0000246
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete la Crosse encephalitis (obsolete MONDO:0000246)","termid":"MONDO:0000246","xrefs":{"Monarch":{"xref_id":"0000246"}}}


id: GO:0061725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of lipid droplets and hydrolysis of stored triglycerides occurring through the orchestrated activation of cytosolic lipases.","definition_xrefs":["GOC:autophagy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid catabolic process","termid":"GO:0016042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"cytosolic lipolysis","termid":"GO:0061725"}


id: PR:Q9P6I6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1198.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6I6"],"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 C1198.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.03c","synonyms":[{"name":"Spom972h-SPBC1198.03c","type":"exact"}],"termid":"PR:Q9P6I6"}


id: SO:0001360
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Five_methoxycarbonylmethyluridine is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_methoxycarbonylmethyluridine","secondary_identifiers":["RNAMOD:068"],"synonyms":[{"name":"5-methoxycarbonylmethyluridine","type":"exact"},{"name":"five methoxycarbonylmethyluridine","type":"exact"},{"name":"mcm5U","type":"exact"}],"termid":"SO:0001360"}


id: PR:Q9P3E5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC750.06c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P3E5"],"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":"UPF0494 membrane protein C750.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC750.06c","synonyms":[{"name":"Spom972h-SPAC750.06c","type":"exact"}],"termid":"PR:Q9P3E5"}


id: GO:0032671
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-27 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-27 production","termid":"GO:0032631"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-27 production","secondary_identifiers":["GO:0045531"],"synonyms":[{"name":"regulation of IL-27 production","type":"exact"},{"name":"regulation of interleukin-27 biosynthetic process","type":"narrow"},{"name":"regulation of interleukin-27 formation","type":"narrow"},{"name":"regulation of interleukin-27 synthesis","type":"narrow"}],"termid":"GO:0032671"}


id: GO:0007415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Separation of a motor axon away from a bundle of axons known as a fascicle.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axonal defasciculation","termid":"GO:0007414"}],"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":"defasciculation of motor neuron axon","termid":"GO:0007415"}


id: MONDO:0008768
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the CLN6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult neuronal ceroid lipofuscinosis","termid":"MONDO:0019260"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005559","MONDO:0002561","MONDO:0005066","MONDO:0002039"],"is_obsolete":false,"name":"ceroid lipofuscinosis, neuronal, 6B (Kufs type)","secondary_identifiers":["MEDGEN:1794137","Orphanet:228340","UMLS:C5561927","DOID:0110730","GARD:6845","OMIM:204300"],"synonyms":[{"name":"CLN4A","type":"exact"},{"name":"CLN4A disease","type":"related"},{"name":"CLN6 neuronal ceroid lipofuscinosis","type":"exact"},{"name":"Kuf's disease type A","type":"related"},{"name":"Kuf's disease, autosomal recessive","type":"related"},{"name":"adult neuronal ceroid lipofuscinosis 4A","type":"related"},{"name":"autosomal recessive neuronal ceroid lipofuscinosis 4A","type":"exact"},{"name":"ceroid lipofuscinosis, neuronal, 4A, autosomal recessive","type":"related"},{"name":"neuronal ceroid lipofuscinosis 4A","type":"exact"},{"name":"neuronal ceroid lipofuscinosis caused by mutation in CLN6","type":"exact"},{"name":"neuronal ceroid lipofuscinosis type 4A","type":"exact"}],"termid":"MONDO:0008768","xrefs":{"Monarch":{"xref_id":"0008768"}}}


id: GO:0035553
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Removal of the methyl group from one or more nucleotides within a single-stranded RNA molecule involving the oxidation (i.e. electron loss) of one or more atoms.","definition_xrefs":["PMID:18775698","GOC:rl","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete oxidative single-stranded RNA demethylation (obsolete GO:0035553)","synonyms":[{"name":"oxidative ssRNA demethylation","type":"exact"}],"termid":"GO:0035553"}


id: GO:0033520
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phytol, (2E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diterpenoid biosynthetic process","termid":"GO:0016102"},{"relation_name":"is_a","term_name":"phytol metabolic process","termid":"GO:0033306"},{"relation_name":"is_a","term_name":"primary alcohol biosynthetic process","termid":"GO:0034309"},{"relation_name":"is_a","term_name":"fatty alcohol biosynthetic process","termid":"GO:1903175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"phytol biosynthetic process","synonyms":[{"name":"phytol anabolism","type":"exact"},{"name":"phytol biosynthesis","type":"exact"},{"name":"phytol formation","type":"exact"},{"name":"phytol synthesis","type":"exact"}],"termid":"GO:0033520"}


id: PBO:0108762
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ageing-Associated LncRNA","termid":"PBO:0108762"}


id: PBO:0055810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysophosphatidylglycerol acyltransferase 1","termid":"PBO:0055810"}


id: PBO:0086206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that associates with ribosomes; homolog of translationally controlled tumor protein; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and relocates to the mitochondrial outer surface upon oxidative stress; homolog of human TPT1","termid":"PBO:0086206"}


