# terms

id: MONDO:0011210
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":"mitochondrial intermembrane space protein Tim12, yeast, homolog of","secondary_identifiers":["OMIM:602252","UMLS:C1865698","MEDGEN:400824"],"synonyms":[{"name":"mitochondrial intermembrane space protein Tim12, yeast, homolog of","type":"exact"}],"termid":"MONDO:0011210","xrefs":{"Monarch":{"xref_id":"0011210"}}}


id: GO:1903440
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of amylin receptor activity.","definition_xrefs":["PMID:12037140","GO_REF:0000088","GOC:bhm","PMID:10871296","PMID:18687416","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcitonin family receptor complex","termid":"GO:1903439"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"amylin receptor complex","termid":"GO:1903440"}


id: MONDO:0003930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Stage 0 includes: 0a (Ta, N0, M0); 0is (Tis, N0, M0). Ta: Noninvasive papillary carcinoma. Tis: Carcinoma in situ: \\\"flat tumor\\\". N0: No regional lymph node metastasis. M0: No distant metastasis. (AJCC 6th and 7th eds.)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bladder transitional cell carcinoma","termid":"MONDO:0005611"}],"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":"non-invasive bladder urothelial carcinoma","secondary_identifiers":["MEDGEN:233466","UMLS:C1336089","DOID:6571","NCIT:C6188"],"synonyms":[{"name":"non-invasive bladder urothelial carcinoma","type":"exact"},{"name":"stage 0 bladder urothelial cancer","type":"exact"},{"name":"stage 0 bladder urothelial carcinoma","type":"exact"},{"name":"stage 0 bladder urothelial carcinoma aJCC v6","type":"exact"},{"name":"stage 0 bladder urothelial carcinoma aJCC v6 and v7","type":"exact"},{"name":"stage 0 bladder urothelial carcinoma aJCC v7","type":"exact"},{"name":"stage 0 transitional cell carcinoma of bladder","type":"exact"},{"name":"stage 0 transitional cell carcinoma of the bladder","type":"exact"},{"name":"stage 0 transitional cell carcinoma of the urinary bladder","type":"exact"},{"name":"stage 0 transitional cell carcinoma of urinary bladder","type":"exact"},{"name":"stage 0 urinary bladder transitional cell carcinoma","type":"exact"}],"termid":"MONDO:0003930","xrefs":{"Monarch":{"xref_id":"0003930"}}}


id: FYPO:0000499
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitophagy does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"},{"relation_name":"is_a","term_name":"abnormal mitophagy","termid":"FYPO:0007590"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abolished mitophagy","synonyms":[{"name":"abolished autophagy of mitochondrion","type":"exact"},{"name":"absent mitophagy","type":"exact"},{"name":"mitophagy abolished","type":"exact"},{"name":"mitophagy: absent","type":"related"}],"termid":"FYPO:0000499"}


id: GO:0050231
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: carbamoyl phosphate + putrescine = N-carbamoylputrescine + H+ + phosphate.","definition_xrefs":["RHEA:21936","EC:2.1.3.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxyl- or carbamoyltransferase activity","termid":"GO:0016743"}],"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:0016741"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016741","GO:0016740"],"is_obsolete":false,"name":"putrescine carbamoyltransferase activity","secondary_identifiers":["MetaCyc:PUTRESCINE-CARBAMOYLTRANSFERASE-RXN","KEGG_REACTION:R01399"],"synonyms":[{"name":"PTCase activity","type":"related"},{"name":"carbamoyl-phosphate:putrescine carbamoyltransferase activity","type":"related"},{"name":"putrescine synthase activity","type":"related"},{"name":"putrescine transcarbamylase activity","type":"related"}],"termid":"GO:0050231"}


id: GO:0001836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in the movement of cytochrome c from the mitochondrial intermembrane space into the cytosol, which is part of the apoptotic signaling pathway and leads to caspase activation.","definition_xrefs":["PMID:12925707","PMID:9560217","GOC:add","GOC:mah","GOC:mtg_apoptosis","ISBN:0721639976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic mitochondrial changes","termid":"GO:0008637"},{"relation_name":"part_of","term_name":"apoptotic signaling pathway","termid":"GO:0097190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0007005","GO:0023052"],"is_obsolete":false,"name":"release of cytochrome c from mitochondria","termid":"GO:0001836"}


id: GO:0010927
data:
  {"annotated_genes":["SJAG_00405","SJAG_02169","SJAG_03536","SJAG_03013","SJAG_02248","SJAG_04922","SJAG_02529","SJAG_03746","SJAG_00514","SJAG_02736","SJAG_01993","SJAG_02700","SJAG_05309","SJAG_04509","SJAG_04781","SJAG_01769","SJAG_01943","SJAG_00486","SJAG_04470","SJAG_00821","SJAG_03688","SJAG_02864","SJAG_04271","SJAG_01894","SJAG_04080","SJAG_03453","SJAG_04868","SJAG_01483","SJAG_00663","SJAG_01794","SJAG_04275","SJAG_04010","SJAG_01321","SJAG_04483","SJAG_03250","SJAG_00971","SJAG_02320","SJAG_00114","SJAG_04901","SJAG_02989","SJAG_03915","SJAG_02379","SJAG_04615","SJAG_00826","SJAG_02241","SJAG_00974"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90072,92118,93654,90566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030476"},{"annotations":[74761,93381,106925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031321"},{"annotations":[99466,109344,93170,115926,97274,120565,120866,101825,100743,121049,99503,112091,103641,107237],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032120"},{"annotations":[108789,115927,106062,101755,98782,101754,109675,94172,104853,99467],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031322"},{"annotations":[100895,116322,94395,90120,100201,100813],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1904600"},{"annotations":[92600],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903024"},{"annotations":[89751,113351,92720,95358,91739],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902917"},{"annotations":[118940],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903023"},{"annotations":[101756,107967,117973,101757,96400,102043],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070583"}]},"cv_name":"biological_process","definition":"The cellular component assembly that is part of the initial shaping of the component during its developmental progression.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"cellular anatomical entity morphogenesis","termid":"GO:0032989"}],"gene_count":46,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_00405":null,"SJAG_00486":null,"SJAG_00514":null,"SJAG_00663":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00971":null,"SJAG_00974":null,"SJAG_01321":null,"SJAG_01483":null,"SJAG_01769":null,"SJAG_01794":null,"SJAG_01894":null,"SJAG_01943":null,"SJAG_01993":null,"SJAG_02169":null,"SJAG_02241":null,"SJAG_02248":null,"SJAG_02320":null,"SJAG_02379":null,"SJAG_02529":null,"SJAG_02700":null,"SJAG_02736":null,"SJAG_02864":null,"SJAG_02989":null,"SJAG_03013":null,"SJAG_03250":null,"SJAG_03453":null,"SJAG_03536":null,"SJAG_03688":null,"SJAG_03746":null,"SJAG_03915":null,"SJAG_04010":null,"SJAG_04080":null,"SJAG_04271":null,"SJAG_04275":null,"SJAG_04470":null,"SJAG_04483":null,"SJAG_04509":null,"SJAG_04615":null,"SJAG_04781":null,"SJAG_04868":null,"SJAG_04901":null,"SJAG_04922":null,"SJAG_05309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"cellular component assembly involved in morphogenesis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0010927","terms_by_termid":{"GO:0030476":null,"GO:0031321":null,"GO:0031322":null,"GO:0032120":null,"GO:0070583":null,"GO:1902917":null,"GO:1903023":null,"GO:1903024":null,"GO:1904600":null}}


id: MONDO:0006104
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carotid body paraganglioma that is confined to the site of origin, without metastatic potential.","definition_xrefs":["NCIT:C79950"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign endocrine neoplasm","termid":"MONDO:0000627"},{"relation_name":"is_a","term_name":"carotid body paraganglioma","termid":"MONDO:0021053"},{"relation_name":"is_a","term_name":"benign blood vessel neoplasm","termid":"MONDO:0024286"},{"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 carotid body paraganglioma","secondary_identifiers":["MEDGEN:396868","UMLS:C2698359","EFO:1000108"],"synonyms":[{"name":"benign carotid body paraganglioma","type":"exact"},{"name":"benign chemodectoma","type":"related"},{"name":"carotid body paraganglioma, benign","type":"exact"},{"name":"chemodectoma, benign","type":"related"}],"termid":"MONDO:0006104","xrefs":{"Monarch":{"xref_id":"0006104"}}}


id: GO:0072374
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-carotene + O2 + reduced [NADPH--hemoprotein reductase] = alpha-cryptoxanthin + H(+) + H2O + oxidized [NADPH--hemoprotein reductase]. Zeinoxanthin may also be used as the substrate, in which case lutein is produced.","definition_xrefs":["EC:1.14.14.158","PMID:8837513"],"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: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":"carotene epsilon hydroxylase activity","termid":"GO:0072374"}


id: PBO:0082865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Core Sm protein Sm E; part of heteroheptameric complex (with Smb1p, Smd1p, Smd2p, Smd3p, Smx3p, and Smx2p) that is part of the spliceosomal U1, U2, U4, and U5 snRNPs; homolog of human Sm E","termid":"PBO:0082865"}


id: PBO:0004744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin beta Nda3","termid":"PBO:0004744"}


id: PBO:0080681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WAS/WASL interacting protein family member 1","termid":"PBO:0080681"}


id: PBO:0036077
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-stubby_vegetative_cell","termid":"PBO:0036077"}


id: GO:0031908
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membranes of a glyoxysome.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisomal matrix","termid":"GO:0005782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005777"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005777","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"glyoxysomal lumen","termid":"GO:0031908"}


id: PBO:0044429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily A member 11","termid":"PBO:0044429"}


id: PBO:0050866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inhibitor of DNA binding 3","termid":"PBO:0050866"}


id: PBO:0072658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retrotransposon Gag like 10","termid":"PBO:0072658"}


id: GO:0006018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of deoxyribose 1-phosphate, the phosphorylated sugar 1-phospho-2-deoxyribose.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-deoxyribose 1-phosphate metabolic process","termid":"GO:0046384"},{"relation_name":"is_a","term_name":"deoxyribose phosphate catabolic process","termid":"GO:0046386"}],"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":"2-deoxyribose 1-phosphate catabolic process","synonyms":[{"name":"2-deoxyribose 1-phosphate breakdown","type":"exact"},{"name":"2-deoxyribose 1-phosphate catabolism","type":"exact"},{"name":"2-deoxyribose 1-phosphate degradation","type":"exact"},{"name":"deoxyribose 1-phosphate catabolic process","type":"exact"}],"termid":"GO:0006018"}


id: GO:0006302
data:
  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id: PBO:0068618
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 70, pseudogene","termid":"PBO:0068618"}


id: PBO:0082647
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of serine palmitoyltransferase; responsible along with Lcb1p for the first committed step in sphingolipid synthesis, which is the condensation of serine with palmitoyl-CoA to form 3-ketosphinganine","termid":"PBO:0082647"}


id: MONDO:0016001
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  {"annotated_genes":["SJAG_03804","SJAG_04362","SJAG_01872"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014072"},{"annotations":[87304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024554"},{"annotations":[88901],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013345"}]},"cv_name":"mondo","definition":"2-Hydroxyglutaric aciduria is a group of neurometabolic disorders with a wide clinical spectrum ranging from severe neonatal presentations to progressive forms, and asymptomatic cases, characterized biochemically by increased levels of 2-hydroxyglutaric acid in the plasma, cerebrospinal fluid and urine.","definition_xrefs":["Orphanet:19"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01872":null,"SJAG_03804":null,"SJAG_04362":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"2-hydroxyglutaric aciduria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C128187","SCTID:698870008","UMLS:C2746066","GARD:10761","DOID:0050573","MEDGEN:412535","ICD9:270.8","MESH:C535306"],"synonyms":[{"name":"2-HGA","type":"related"},{"name":"2-hydroxyglutaric acidemia","type":"exact"},{"name":"2-hydroxyglutaric aciduria","type":"exact"}],"termid":"MONDO:0016001","terms_by_termid":{"MONDO:0013345":null,"MONDO:0014072":null,"MONDO:0024554":null},"xrefs":{"Monarch":{"xref_id":"0016001"}}}


id: PBO:0038681
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA synthetase medium chain family member 6","termid":"PBO:0038681"}


id: PBO:0085611
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in DNA mismatch repair and meiotic recombination; involved in crossing-over during meiotic recombination; forms a complex with Mlh1p; mammalian homolog is implicated mammalian microsatellite instability","termid":"PBO:0085611"}


id: PBO:0056726
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MER proto-oncogene, tyrosine kinase","termid":"PBO:0056726"}


id: PR:P40921
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC29A4.02c gene.","definition_xrefs":["PRO:DNx","UniProtKB:P40921"],"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":"elongation factor 1-gamma (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.02c","synonyms":[{"name":"EF-1-gamma (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPAC29A4.02c","type":"exact"},{"name":"eEF-1B gamma (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P40921"}


id: PBO:0070856
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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 L13 pseudogene 9","termid":"PBO:0070856"}


id: FYPO:0006270
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to phosphate starvation is higher than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"},{"relation_name":"is_a","term_name":"altered RNA level during cellular response to phosphate starvation","termid":"FYPO:0003195"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0006551","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased RNA level during cellular response to phosphate starvation","synonyms":[{"name":"increased RNA accumulation during cellular response to phosphate starvation","type":"related"},{"name":"increased RNA level during cellular response to phosphate depletion","type":"exact"},{"name":"increased RNA level during cellular response to phosphate deprivation","type":"exact"},{"name":"increased RNA level during cellular response to phosphate starvation during mitotic cell cycle","type":"related"},{"name":"increased RNA level during cellular response to phosphate starvation during vegetative growth","type":"exact"},{"name":"increased RNA level during phosphate starvation","type":"exact"},{"name":"increased mRNA level during cellular response to phosphate starvation","type":"narrow"},{"name":"increased transcript level during cellular response to phosphate starvation","type":"exact"}],"termid":"FYPO:0006270"}


id: FYPO:0005507
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  {"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 mature ribosomal RNA (rRNA) measured in a cell is higher than normal. Total rRNA or a specific rRNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered mature rRNA level during vegetative growth","termid":"FYPO:0006468"},{"relation_name":"is_a","term_name":"increased ncRNA level during vegetative growth","termid":"FYPO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0006551","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased mature rRNA level","synonyms":[{"name":"increased mature rRNA accumulation","type":"related"},{"name":"increased mature rRNA level during mitotic cell cycle","type":"related"},{"name":"increased mature rRNA level during vegetative growth","type":"exact"},{"name":"increased mature rRNA transcript level","type":"broad"},{"name":"increased mature ribosomal RNA level","type":"exact"},{"name":"increased rRNA level","type":"broad"}],"termid":"FYPO:0005507"}


id: PBO:0046949
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 74 member A3","termid":"PBO:0046949"}


id: PBO:0070930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 38","termid":"PBO:0070930"}


id: SO:0000241
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  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A UTR bordered by the terminal and initial codons of two CDSs in a polycistronic transcript. Every UTR is either 5', 3' or internal.","definition_xrefs":["SO:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UTR","termid":"SO:0000203"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"internal_UTR","synonyms":[{"name":"internal UTR","type":"exact"}],"termid":"SO:0000241"}


id: PBO:0064170
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group IVF","termid":"PBO:0064170"}


id: PBO:0087818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFIID subunit (19 kDa); involved in RNA polymerase II transcription initiation, similar to histone H4 with atypical histone fold motif of Spt3-like transcription factors","termid":"PBO:0087818"}


id: MONDO:0004342
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  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete osteoclast-like giant cell neoplasm of the pancreas (obsolete MONDO:0004342)","termid":"MONDO:0004342","xrefs":{"Monarch":{"xref_id":"0004342"}}}


id: PATO:0002502
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  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An orientation quality inhering in a bearer by virtue of the bearer having a position that is directed transversely.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orientation","termid":"PATO:0000133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transverse orientation","synonyms":[{"name":"transversely oriented","type":"exact"}],"termid":"PATO:0002502"}


id: PR:Q9UTS7
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC977.12 gene.","definition_xrefs":["UniProtKB:Q9UTS7","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":"L-asparaginase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC977.12","synonyms":[{"name":"L-asparagine amidohydrolase 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPAC977.12","type":"exact"}],"termid":"PR:Q9UTS7"}


id: MONDO:0001405
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dermatophytosis involving the stratum corneum of the skin of the groin and perianal area.","definition_xrefs":["NCIT:C34535"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatophytosis","termid":"MONDO:0004678"}],"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":"dermatophytosis of groin and perianal area","secondary_identifiers":["DOID:11917","ICD9:110.3","UMLS:C0011638","MEDGEN:3769","SCTID:399029005"],"synonyms":[{"name":"Dhobie itch","type":"exact"},{"name":"dermatophytosis of groin & perianal area","type":"exact"},{"name":"dermatophytosis of groin and perianal area","type":"exact"},{"name":"tinea cruris","type":"related"}],"termid":"MONDO:0001405","xrefs":{"Monarch":{"xref_id":"0001405"}}}


id: GO:0031253
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  {"annotated_genes":["SJAG_01978","SJAG_02989"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89997,100893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070250"}]},"cv_name":"cellular_component","definition":"The portion of the plasma membrane surrounding a plasma membrane bounded cell surface projection.","definition_xrefs":["GOC:krc","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"},{"relation_name":"part_of","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01978":null,"SJAG_02989":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"cell projection membrane","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"membrane extension","type":"related"},{"name":"membrane projection","type":"related"}],"termid":"GO:0031253","terms_by_termid":{"GO:0070250":null}}


id: GO:0061691
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  {"annotated_genes":["SJAG_01199","SJAG_04953","SJAG_00141","SJAG_02515","SJAG_01216","SJAG_04823"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119379,97098,101922,120320,106996,110806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061692"}]},"cv_name":"biological_process","definition":"Any process that reduces or removes the toxicity of hydrogen peroxide. These include transport of hydrogen peroxide away from sensitive areas and to compartments or complexes whose purpose is sequestration.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrogen peroxide metabolic process","termid":"GO:0042743"},{"relation_name":"is_a","term_name":"detoxification of inorganic compound","termid":"GO:0061687"},{"relation_name":"part_of","term_name":"response to hydrogen peroxide","termid":"GO:0042542"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00141":null,"SJAG_01199":null,"SJAG_01216":null,"SJAG_02515":null,"SJAG_04823":null,"SJAG_04953":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098754"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"detoxification of hydrogen peroxide","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061691","terms_by_termid":{"GO:0061692":null}}


id: MOD:00470
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  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:92"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NHS-LC-Biotin","synonyms":[{"name":"NHS-LC-Biotin","type":"related"}],"termid":"MOD:00470"}


id: MONDO:0013123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any atrial heart septal defect in which the cause of the disease is a mutation in the TLL1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrial septal defect","termid":"MONDO:0006664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"atrial septal defect 6","secondary_identifiers":["DOID:0110111","MESH:C567764","OMIM:613087","UMLS:C2751315","MEDGEN:414348"],"synonyms":[{"name":"ASD6","type":"exact"},{"name":"TLL1 atrial heart septal defect","type":"exact"},{"name":"atrial heart septal defect caused by mutation in TLL1","type":"exact"},{"name":"atrial heart septal defect type 6","type":"exact"},{"name":"atrial septal defect 6","type":"exact"},{"name":"atrial septal defect type 6","type":"exact"}],"termid":"MONDO:0013123","xrefs":{"Monarch":{"xref_id":"0013123"}}}


id: GO:0008511
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: Na+(out) + K+(out) + Cl-(out) = Na+(in) + K+(in) + Cl-(in).","definition_xrefs":["TC:2.A.30.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium:sodium symporter activity","termid":"GO:0009674"},{"relation_name":"is_a","term_name":"sodium:chloride symporter activity","termid":"GO:0015378"},{"relation_name":"is_a","term_name":"potassium:chloride symporter activity","termid":"GO:0015379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"sodium:potassium:chloride symporter activity","secondary_identifiers":["Reactome:R-HSA-5623588","Reactome:R-HSA-426086","RHEA:72395"],"synonyms":[{"name":"sodium/potassium/chloride symporter activity","type":"exact"}],"termid":"GO:0008511"}


id: PBO:0049636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 39","termid":"PBO:0049636"}


id: GO:0051105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of DNA ligation, the re-formation of a broken phosphodiester bond in the DNA backbone, carried out by DNA ligase.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of DNA ligation (obsolete GO:0051105)","termid":"GO:0051105"}


id: MONDO:0012384
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial panic disorder","termid":"MONDO:0031240"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"panic disorder 3","secondary_identifiers":["OMIM:609985","UMLS:C1864946","MEDGEN:400645"],"synonyms":[{"name":"Pand3","type":"related"},{"name":"panic disorder 3","type":"exact"},{"name":"panic disorder susceptibility locus, chromosome 4Q-related","type":"related"},{"name":"panic disorder type 3","type":"exact"}],"termid":"MONDO:0012384","xrefs":{"Monarch":{"xref_id":"0012384"}}}


id: PBO:0004928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi transport complex subunit Cog3 (predicted)","termid":"PBO:0004928"}


id: MONDO:0018804
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive familial intrahepatic cholestasis","termid":"MONDO:0015762"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335","MONDO:0005066"],"is_obsolete":false,"name":"MYO5B-related progressive familial intrahepatic cholestasis","secondary_identifiers":["MEDGEN:1826070","Orphanet:480491","GARD:21972","UMLS:C5680100"],"synonyms":[{"name":"MYO5B deficiency","type":"exact"}],"termid":"MONDO:0018804","xrefs":{"Monarch":{"xref_id":"0018804"}}}


id: PBO:0064988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein regulator of cytokinesis 1","termid":"PBO:0064988"}


id: PBO:0069849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1135, pseudogene","termid":"PBO:0069849"}


id: GO:0098506
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of removing one or more phosphate groups from the 3' end of a polynucleotide.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleobase-containing compound metabolic process","termid":"GO:0006139"},{"relation_name":"is_a","term_name":"dephosphorylation","termid":"GO:0016311"},{"relation_name":"is_a","term_name":"macromolecule metabolic process","termid":"GO:0043170"}],"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":"polynucleotide 3' dephosphorylation","termid":"GO:0098506"}


id: PBO:0051544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 6 cytokine family signal transducer","termid":"PBO:0051544"}


id: PBO:0080587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WDR11 divergent transcript","termid":"PBO:0080587"}


id: SO:0000620
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variably distant linear promoter region recognized by TFIIIC, with consensus sequence AGGTTCCAnnCC.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"core_eukaryotic_promoter_element","termid":"SO:0001660"},{"relation_name":"part_of","term_name":"RNApol_III_promoter_type_2","termid":"SO:0000618"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B_box","synonyms":[{"name":"B-box","type":"exact"}],"termid":"SO:0000620"}


id: PBO:0063947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PINK1 antisense RNA","termid":"PBO:0063947"}


id: GO:1904982
data:
  {"annotated_genes":["SJAG_03960"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106082"}]},"cv_name":"biological_process","definition":"The process in which sucrose is transported across a membrane.","definition_xrefs":["PMID:11136464","GO_REF:0000069","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sucrose transport","termid":"GO:0015770"},{"relation_name":"is_a","term_name":"carbohydrate transmembrane transport","termid":"GO:0034219"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03960":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:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"sucrose transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1904982","terms_by_termid":{"GO:0106082":null}}


id: GO:0046830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of movement of RNA from the cytoplasm into the nucleus.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of nucleobase-containing compound transport","termid":"GO:0032241"},{"relation_name":"is_a","term_name":"positive regulation of nucleocytoplasmic transport","termid":"GO:0046824"},{"relation_name":"is_a","term_name":"regulation of RNA import into nucleus","termid":"GO:0046828"},{"relation_name":"positively_regulates","term_name":"RNA import into nucleus","termid":"GO:0006404"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006913"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006913"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006913","GO:0006810"],"is_obsolete":false,"name":"positive regulation of RNA import into nucleus","synonyms":[{"name":"activation of RNA import into nucleus","type":"narrow"},{"name":"positive regulation of RNA import into cell nucleus","type":"exact"},{"name":"positive regulation of RNA transport from cytoplasm to nucleus","type":"exact"},{"name":"positive regulation of RNA-nucleus import","type":"exact"},{"name":"stimulation of RNA import into nucleus","type":"narrow"},{"name":"up regulation of RNA import into nucleus","type":"exact"},{"name":"up-regulation of RNA import into nucleus","type":"exact"},{"name":"upregulation of RNA import into nucleus","type":"exact"}],"termid":"GO:0046830"}


id: MONDO:0004017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"malignant pineal area germ cell neoplasm","termid":"MONDO:0002073"},{"relation_name":"is_a","term_name":"malignant teratoma","termid":"MONDO:0003514"},{"relation_name":"is_a","term_name":"extragonadal nonseminomatous germ cell tumor","termid":"MONDO:0003578"},{"relation_name":"is_a","term_name":"central nervous system immature teratoma","termid":"MONDO:0003735"},{"relation_name":"is_a","term_name":"pineal region teratoma","termid":"MONDO:0004015"},{"relation_name":"is_a","term_name":"immature teratoma","termid":"MONDO:0024746"}],"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":"pineal region immature teratoma","secondary_identifiers":["UMLS:C1335416","DOID:6858","NCIT:C6755","MEDGEN:277516"],"synonyms":[{"name":"atypical pineal teratoma","type":"exact"},{"name":"immature teratoma of pineal area","type":"exact"},{"name":"immature teratoma of pineal region","type":"exact"},{"name":"immature teratoma of the pineal area","type":"exact"},{"name":"immature teratoma of the pineal region","type":"exact"},{"name":"pineal area immature teratoma","type":"exact"}],"termid":"MONDO:0004017","xrefs":{"Monarch":{"xref_id":"0004017"}}}


id: PBO:0068623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 3, pseudogene","termid":"PBO:0068623"}


id: MONDO:0024646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete refractory (obsolete MONDO:0024646)","secondary_identifiers":["NCIT:C39752"],"termid":"MONDO:0024646","xrefs":{"Monarch":{"xref_id":"0024646"}}}


id: PBO:0031420
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_DNA_damage_checkpoint","termid":"PBO:0031420"}


id: PBO:0045064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLG3 antisense RNA 1","termid":"PBO:0045064"}


id: MONDO:0019568
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Ehlers-Danlos syndrome in which the cause of the disease is a mutation in the COL5A2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome, classic type","termid":"MONDO:0007522"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Ehlers-Danlos syndrome, classic type, 2","secondary_identifiers":["OMIM:130010","NCIT:C125697","MESH:C536195","Orphanet:90318","UMLS:C0268336","DOID:0080726","MEDGEN:120628"],"synonyms":[{"name":"EDS II","type":"exact"},{"name":"EDS II, formerly","type":"related"},{"name":"EDSCL2","type":"exact"},{"name":"Ehlers Danlos syndrome, mild Classic type","type":"related"},{"name":"Ehlers Danlos syndrome, mild Classic type, formerly","type":"related"},{"name":"Ehlers Danlos syndrome, mitis type","type":"related"},{"name":"Ehlers Danlos syndrome, mitis type, formerly","type":"related"},{"name":"Ehlers-Danlos syndrome, classic type, 2","type":"exact"},{"name":"Ehlers-Danlos syndrome, type Ii","type":"related"},{"name":"Ehlers-Danlos syndrome, type Ii, formerly","type":"related"}],"termid":"MONDO:0019568","xrefs":{"Monarch":{"xref_id":"0019568"}}}


id: GO:1905494
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of G-quadruplex DNA binding.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:26503245"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of G-quadruplex DNA binding (obsolete GO:1905494)","synonyms":[{"name":"down regulation of G quadruplex DNA binding","type":"exact"},{"name":"down regulation of G quartet DNA binding","type":"exact"},{"name":"down regulation of G-DNA binding","type":"exact"},{"name":"down regulation of G-quadruplex DNA binding","type":"exact"},{"name":"down regulation of G-quartet DNA binding","type":"exact"},{"name":"down regulation of quadruplex DNA binding","type":"exact"},{"name":"down regulation of tetraplex DNA binding","type":"exact"},{"name":"down-regulation of G quadruplex DNA binding","type":"exact"},{"name":"down-regulation of G quartet DNA binding","type":"exact"},{"name":"down-regulation of G-DNA binding","type":"exact"},{"name":"down-regulation of G-quadruplex DNA binding","type":"exact"},{"name":"down-regulation of G-quartet DNA binding","type":"exact"},{"name":"down-regulation of quadruplex DNA binding","type":"exact"},{"name":"down-regulation of tetraplex DNA binding","type":"exact"},{"name":"downregulation of G quadruplex DNA binding","type":"exact"},{"name":"downregulation of G quartet DNA binding","type":"exact"},{"name":"downregulation of G-DNA binding","type":"exact"},{"name":"downregulation of G-quadruplex DNA binding","type":"exact"},{"name":"downregulation of G-quartet DNA binding","type":"exact"},{"name":"downregulation of quadruplex DNA binding","type":"exact"},{"name":"downregulation of tetraplex DNA binding","type":"exact"},{"name":"inhibition of G quadruplex DNA binding","type":"narrow"},{"name":"inhibition of G quartet DNA binding","type":"narrow"},{"name":"inhibition of G-DNA binding","type":"narrow"},{"name":"inhibition of G-quadruplex DNA binding","type":"narrow"},{"name":"inhibition of G-quartet DNA binding","type":"narrow"},{"name":"inhibition of quadruplex DNA binding","type":"narrow"},{"name":"inhibition of tetraplex DNA binding","type":"narrow"},{"name":"negative regulation of G quadruplex DNA binding","type":"exact"},{"name":"negative regulation of G quartet DNA binding","type":"exact"},{"name":"negative regulation of G-DNA binding","type":"exact"},{"name":"negative regulation of G-quartet DNA binding","type":"exact"},{"name":"negative regulation of quadruplex DNA binding","type":"exact"},{"name":"negative regulation of tetraplex DNA binding","type":"exact"}],"termid":"GO:1905494"}


id: PBO:0075957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal transducing adaptor family member 1","termid":"PBO:0075957"}


id: MONDO:0001819
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"glossopharyngeal nerve disorder","termid":"MONDO:0002639"},{"relation_name":"is_a","term_name":"cranial nerve palsy","termid":"MONDO:0002782"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple cranial nerve palsy","secondary_identifiers":["MEDGEN:509636","DOID:13866","SCTID:78152008","UMLS:C0154733","ICD9:352.6"],"synonyms":[{"name":"multiple cranial nerve palsies","type":"exact"}],"termid":"MONDO:0001819","xrefs":{"Monarch":{"xref_id":"0001819"}}}


id: PBO:0045479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"desmocollin 1","termid":"PBO:0045479"}


id: PBO:0052357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIF5C antisense RNA 1","termid":"PBO:0052357"}


id: PBO:0044760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 43 pseudogene 1","termid":"PBO:0044760"}


id: GO:2000514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of CD4-positive, alpha-beta T cell activation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of alpha-beta T cell activation","termid":"GO:0046634"},{"relation_name":"regulates","term_name":"CD4-positive, alpha-beta T cell activation","termid":"GO:0035710"}],"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 CD4-positive, alpha-beta T cell activation","termid":"GO:2000514"}


id: FYPO:0003164
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which nuclease activity is absent. All nuclease activities may be absent, or a specific nuclease activity may be assayed.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished catalytic activity","termid":"FYPO:0000664"},{"relation_name":"is_a","term_name":"abnormal nuclease activity","termid":"FYPO:0003163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000707","FYPO:0001985","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"abolished nuclease activity","synonyms":[{"name":"nuclease activity abolished","type":"exact"}],"termid":"FYPO:0003164"}


id: PBO:0075222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 1","termid":"PBO:0075222"}


id: MONDO:1012829
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ichthyosis that occurs in cattle due to a mutation in the DSP gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"ichthyosis, cattle","termid":"MONDO:1011541"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ichthyosis, DSP-related, cattle","secondary_identifiers":["OMIA:002243-9913"],"termid":"MONDO:1012829","xrefs":{"Monarch":{"xref_id":"1012829"}}}


id: MONDO:0026721
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, nuclear type","termid":"MONDO:0100223"},{"relation_name":"is_a","term_name":"NDUFB11-related disorders","termid":"MONDO:1040023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial complex 1 deficiency, nuclear type 30","secondary_identifiers":["OMIM:301021","DOID:0112098","GARD:15284","UMLS:C4746985","MEDGEN:1648313"],"synonyms":[{"name":"MC1DN30","type":"related"},{"name":"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30","type":"related"}],"termid":"MONDO:0026721","xrefs":{"Monarch":{"xref_id":"0026721"}}}


id: FYPO:0002013
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 protein oxidation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein modification during vegetative growth","termid":"FYPO:0000549"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal protein oxidation during vegetative growth","synonyms":[{"name":"normal protein oxidation during mitotic cell cycle","type":"related"},{"name":"normal protein/peptide oxidation during vegetative growth","type":"exact"}],"termid":"FYPO:0002013"}


id: GO:0043102
data:
  {"annotated_genes":["SJAG_03881","SJAG_00309","SJAG_01404","SJAG_03614","SJAG_04425","SJAG_02689","SJAG_02293"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59106,78659,79585,80140,81001,82087],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019509"},{"annotations":[100437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019284"}]},"cv_name":"biological_process","definition":"Any process which produces an amino acid from derivatives of it, without de novo synthesis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid biosynthetic process","termid":"GO:0008652"},{"relation_name":"is_a","term_name":"metabolic compound salvage","termid":"GO:0043094"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00309":null,"SJAG_01404":null,"SJAG_02293":null,"SJAG_02689":null,"SJAG_03614":null,"SJAG_03881":null,"SJAG_04425":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0008150"],"is_obsolete":false,"name":"amino acid salvage","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"termid":"GO:0043102","terms_by_termid":{"GO:0019284":null,"GO:0019509":null}}


id: MONDO:0007187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare hereditary disorder due to autosomal dominant transmission with hamartosis characterized by multiple early-onset basal cell carcinoma (BCC), multiple jaw keratocysts and skeletal abnormalities.","definition_xrefs":["Orphanet:377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"is_a","term_name":"neurocutaneous syndrome","termid":"MONDO:0042983"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"nevoid basal cell carcinoma syndrome","secondary_identifiers":["NCIT:C2892","SCTID:69408002","MEDGEN:2554","NORD:1507","GARD:7166","DOID:0070365","DOID:2512","MESH:D001478","UMLS:C0004779","OMIMPS:109400","MedDRA:10062804","icd11.foundation:1012745138","NANDO:2200828"],"synonyms":[{"name":"BCNS","type":"related"},{"name":"Gorlin syndrome","type":"exact"},{"name":"Gorlin-Goltz syndrome","type":"exact"},{"name":"NBCCS","type":"exact"},{"name":"basal cell nevus syndrome","type":"exact"},{"name":"multiple basal cell carcinomas","type":"exact"},{"name":"multiple basal cell nevi, odontogenic keratocysts, and skeletal anomalies","type":"related"},{"name":"nevoid basal cell cancer syndrome","type":"exact"},{"name":"nevoid basal cell carcinoma syndrome","type":"exact"}],"termid":"MONDO:0007187","xrefs":{"Monarch":{"xref_id":"0007187"}}}


id: MONDO:0012241
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the TWNK gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant progressive external ophthalmoplegia","termid":"MONDO:0008003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069","MONDO:0005336","MONDO:0000426","MONDO:0002320"],"is_obsolete":false,"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3","secondary_identifiers":["UMLS:C1836439","MEDGEN:373087","GARD:16499","OMIM:609286","MESH:C563747","DOID:0111520"],"synonyms":[{"name":"PEOA3","type":"related"},{"name":"TWNK progressive external ophthalmoplegia with mitochondrial DNA deletions","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in TWNK","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 3","type":"exact"},{"name":"progressive external ophthalmoplegia, autosomal dominant 3","type":"related"}],"termid":"MONDO:0012241","xrefs":{"Monarch":{"xref_id":"0012241"}}}


id: PBO:0012257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteiasome complex subunit Ecm29","termid":"PBO:0012257"}


id: MONDO:0005305
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epistaxis (obsolete MONDO:0005305)","termid":"MONDO:0005305","xrefs":{"Monarch":{"xref_id":"0005305"}}}


id: PBO:0075878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST3 beta-galactoside alpha-2,3-sialyltransferase 5","termid":"PBO:0075878"}


id: PBO:0040580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAALC antisense RNA 2","termid":"PBO:0040580"}


id: GO:0047671
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: anthranilate + 2 ATP + L-phenylalanine + S-adenosyl-L-methionine = 2 AMP + cyclopeptine + 2 diphosphate + 2 H+ + S-adenosyl-L-homocysteine.","definition_xrefs":["PMID:2995633","RHEA:35091","EC:6.3.2.40"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-amino acid ligase activity","termid":"GO:0016881"}],"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:0016874"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"cyclopeptine synthase activity","secondary_identifiers":["MetaCyc:RXN-13989","KEGG_REACTION:R00979"],"synonyms":[{"name":"ATP:anthranilate adenylyltransferase activity","type":"exact"},{"name":"anthranilate adenylyltransferase activity","type":"related"}],"termid":"GO:0047671"}


id: PBO:0077573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA element modulatory factor 1","termid":"PBO:0077573"}


id: MONDO:0003526
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lung giant cell carcinoma (obsolete MONDO:0003526)","termid":"MONDO:0003526","xrefs":{"Monarch":{"xref_id":"0003526"}}}


id: GO:0016259
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving selenocysteine, an essential component of glutathione peroxidase and some other proteins.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine family amino acid metabolic process","termid":"GO:0009069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"selenocysteine metabolic process","secondary_identifiers":["Reactome:R-HSA-2408522"],"synonyms":[{"name":"selenocysteine metabolism","type":"exact"}],"termid":"GO:0016259"}


id: PBO:0045622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 34 (pseudogene)","termid":"PBO:0045622"}


id: PBO:0001874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomerase RNA","termid":"PBO:0001874"}


id: PBO:0055785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LONRF2 pseudogene 5","termid":"PBO:0055785"}


id: GO:0023070
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a signal is conveyed via the air.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signal transmission via air (obsolete GO:0023070)","synonyms":[{"name":"signal transmission via air","type":"exact"}],"termid":"GO:0023070"}


id: PBO:0030608
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_calcium_level","termid":"PBO:0030608"}


id: GO:0140426
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by a ligand binding of a pattern recognition receptor (PRR) to activate a plant innate immune response. PAMP-triggered immunity PRRs bind pathogen-associated molecular pattern (PAMPs), structures conserved among microbial species.","definition_xrefs":["PMID:25744358"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern recognition receptor signaling pathway","termid":"GO:0002221"}],"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":"pathogen-associated molecular pattern receptor signaling pathway","synonyms":[{"name":"MAMP-triggered immunity signalling","type":"exact"},{"name":"PAMP receptor signaling pathway","type":"exact"},{"name":"PAMP-triggered immunity signalling pathway","type":"exact"},{"name":"PTI signalling","type":"exact"},{"name":"pathogen-associated molecular pattern signalling","type":"exact"}],"termid":"GO:0140426"}


id: PBO:0086527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved across S. cerevisiae strains; YFL019C is not an essential gene","termid":"PBO:0086527"}


id: PBO:0034101
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_consecutive_sequence_of","termid":"PBO:0034101"}


id: PATO:0002277
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of certain surfaces which appear to change colour as the angle of view changes.","direct_ancestors":[{"relation_name":"is_a","term_name":"variant color","termid":"PATO:0001615"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iridescent","termid":"PATO:0002277"}


id: MONDO:0000330
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A bacterial infection caused by Rickettsia typhi.","definition_xrefs":["Wikipedia:Murine_typhus"],"direct_ancestors":[{"relation_name":"is_a","term_name":"typhus","termid":"MONDO:0001246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endemic typhus","secondary_identifiers":["NCIT:C84688","DOID:0050481","GARD:19033","icd11.foundation:4659958","MESH:D014437","MedDRA:10028282","Orphanet:83315","UMLS:C0041472","MEDGEN:11977"],"synonyms":[{"name":"Rickettsia felis spotted fever","type":"exact"},{"name":"cat flea rickettsiosis","type":"exact"},{"name":"endemic flea-borne typhus","type":"exact"},{"name":"endemic typhus fever","type":"exact"},{"name":"fleaborne typhus","type":"exact"},{"name":"murine typhus","type":"exact"},{"name":"rat-flea typhus","type":"exact"},{"name":"shop typhus","type":"related"},{"name":"toulon typhus","type":"exact"},{"name":"urban typhus","type":"exact"},{"name":"urban typhus of Malaya","type":"exact"}],"termid":"MONDO:0000330","xrefs":{"Monarch":{"xref_id":"0000330"}}}


id: MONDO:0001778
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign hamartomatous tumor that possesses various epidermal derivatives and is due to sequestration of skin along the lines of embryonic closure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin cancer","termid":"MONDO:0002898"},{"relation_name":"is_a","term_name":"dermoid cyst","termid":"MONDO:0002378"},{"relation_name":"is_a","term_name":"skin neoplasm","termid":"MONDO:0002531"}],"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":"dermoid cyst of skin","secondary_identifiers":["MEDGEN:91148","NCIT:C4632","DOID:13691","UMLS:C0349502","SCTID:276729007"],"synonyms":[{"name":"cutaneous dermoid cyst","type":"exact"},{"name":"cystic skin teratoma","type":"exact"},{"name":"dermoid cyst of skin","type":"exact"},{"name":"dermoid cyst of skin (finding)","type":"exact"},{"name":"dermoid cyst of the skin","type":"exact"},{"name":"skin dermoid","type":"exact"},{"name":"skin dermoid cyst","type":"exact"},{"name":"subcutaneous dermoid cyst","type":"exact"},{"name":"zone of skin dermoid cyst","type":"exact"}],"termid":"MONDO:0001778","xrefs":{"Monarch":{"xref_id":"0001778"}}}


id: MONDO:0003604
data:
  {"annotated_genes":["SJAG_03429"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88567],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"}]},"cv_name":"mondo","definition":"A hormone producing pituitary gland tumor, associated with a hormonal syndrome.","definition_xrefs":["NCIT:C7047"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"pituitary cancer","termid":"MONDO:0002109"},{"relation_name":"is_a","term_name":"pituitary tumor","termid":"MONDO:0017611"},{"relation_name":"is_a","term_name":"functioning endocrine neoplasm","termid":"MONDO:0021120"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03429":null},"genotype_count":0,"is_obsolete":false,"name":"functioning pituitary gland neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0851693","MEDGEN:163414","SCTID:448148000","DOID:5716","ICD9:237.0"],"synonyms":[{"name":"functioning endocrine neoplasm of pituitary gland","type":"exact"},{"name":"functioning pituitary gland neoplasm","type":"exact"},{"name":"functioning pituitary neoplasm","type":"exact"},{"name":"functioning pituitary tumor","type":"related"},{"name":"functioning pituitary tumour","type":"related"},{"name":"growth hormone producing pituitary tumour","type":"related"},{"name":"hormone producing pituitary cancer","type":"related"},{"name":"hormone producing pituitary neoplasm","type":"exact"},{"name":"pituitary gland functioning endocrine neoplasm","type":"exact"},{"name":"pituitary neoplasms, hormone producing","type":"exact"},{"name":"pituitary tumors, hormone producing","type":"exact"},{"name":"secretory pituitary tumor","type":"related"},{"name":"secretory pituitary tumour","type":"related"},{"name":"somatotropinoma","type":"related"}],"termid":"MONDO:0003604","terms_by_termid":{"MONDO:0009050":null},"xrefs":{"Monarch":{"xref_id":"0003604"}}}


id: MONDO:0004588
data:
  {"annotated_genes":["SJAG_03081"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014872"}]},"cv_name":"mondo","definition":"Inability to see clearly in dim light.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blindness (disorder)","termid":"MONDO:0001941"},{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03081":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"night blindness","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:368.69","ICD9:368.6","NCIT:C34850","SCTID:65194006","UMLS:C0028077","MESH:D009755","ICD10CM:H53.6","DOID:8499","MEDGEN:10349","icd11.foundation:205882698","ICD9:368.60"],"synonyms":[{"name":"nyctalopia","type":"exact"}],"termid":"MONDO:0004588","terms_by_termid":{"MONDO:0014872":null},"xrefs":{"Monarch":{"xref_id":"0004588"}}}


id: GO:0038162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by erythropoietin (EPO) binding to the erythropoietin receptor (EPO-R) on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:12489509","GOC:nhn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"},{"relation_name":"part_of","term_name":"cellular response to erythropoietin","termid":"GO:0036018"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"erythropoietin-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-9006335"],"synonyms":[{"name":"EPO-R signaling pathway","type":"exact"},{"name":"erythropoietin receptor signaling pathway","type":"exact"}],"termid":"GO:0038162"}


id: GO:0085012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An interaction with the host organism mediated by a substance secreted by the symbiont organism by a Tat complex. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete interaction with host via protein secreted by Tat complex (obsolete GO:0085012)","synonyms":[{"name":"interaction with host via protein secreted by Tat secretion system","type":"exact"}],"termid":"GO:0085012"}


id: PBO:0042990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHEK2 pseudogene 3","termid":"PBO:0042990"}


id: GO:0061031
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the endodermal digestive tract are generated and organized. The endodermal digestive tract includes those portions of the digestive tract that are derived from endoderm.","definition_xrefs":["GOC:yaf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","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":"endodermal digestive tract morphogenesis","termid":"GO:0061031"}


id: GO:0002784
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of antimicrobial peptide production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of production of molecular mediator of immune response","termid":"GO:0002700"},{"relation_name":"is_a","term_name":"regulation of antimicrobial humoral response","termid":"GO:0002759"},{"relation_name":"regulates","term_name":"antimicrobial peptide production","termid":"GO:0002775"}],"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 antimicrobial peptide production","termid":"GO:0002784"}


id: MONDO:0007356
data:
  {"annotated_genes":["SJAG_02226"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88200],"is_not":false,"summary":null,"term":"MONDO:0007356"}]},"cv_name":"mondo","definition":"Any Lynch syndrome in which the cause of the disease is a mutation in the MSH2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Lynch syndrome","termid":"MONDO:0005835"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"hereditary nonpolyposis colon cancer","termid":"MONDO:0018630"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02226":null},"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:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"Lynch syndrome 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:15052","UMLS:C2936783","MEDGEN:423615","DOID:0070271","NCIT:C6725","MESH:C537261","OMIM:120435"],"synonyms":[{"name":"COCA1","type":"related"},{"name":"HNPCC1","type":"exact"},{"name":"Hereditary non-polyposis colon cancer type 1","type":"exact"},{"name":"LYNCH syndrome I","type":"related"},{"name":"Lynch 1 syndrome","type":"exact"},{"name":"Lynch syndrome 1","type":"exact"},{"name":"Lynch syndrome 2","type":"related"},{"name":"Lynch syndrome type 1","type":"exact"},{"name":"colon cancer, familial nonpolyposis, type 1","type":"related"},{"name":"colorectal cancer, hereditary nonpolyposis, type 1","type":"related"},{"name":"familial non-polyposis colon cancer type 1","type":"exact"},{"name":"hereditary nonpolyposis colorectal cancer type 1","type":"exact"}],"termid":"MONDO:0007356","terms_by_termid":{"MONDO:0007356":null},"xrefs":{"Monarch":{"xref_id":"0007356"}}}


id: PBO:0040736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCR pseudogene 2","termid":"PBO:0040736"}


id: PBO:0046370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleoside triphosphate diphosphohydrolase 5 (inactive)","termid":"PBO:0046370"}


id: MONDO:0003152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"adult brainstem glioma","termid":"MONDO:0003153"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"adult brainstem gliosarcoma","secondary_identifiers":["NCIT:C9370","DOID:4812","UMLS:C1377914","MEDGEN:277992"],"synonyms":[{"name":"adult brain stem gliosarcoma","type":"exact"},{"name":"adult brainstem gliosarcoma","type":"exact"}],"termid":"MONDO:0003152","xrefs":{"Monarch":{"xref_id":"0003152"}}}


id: GO:0002060
data:
  {"annotated_genes":["SJAG_01859"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002055"}]},"cv_name":"molecular_function","definition":"Binding to a purine nucleobase, an organic nitrogenous base with a purine skeleton.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleobase binding","termid":"GO:0002054"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01859":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"purine nucleobase binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"purine base binding","type":"exact"},{"name":"purine binding","type":"related"}],"termid":"GO:0002060","terms_by_termid":{"GO:0002055":null}}


id: PBO:0057858
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3169","termid":"PBO:0057858"}


id: GO:0070079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H4 by the removal of a methyl group from arginine at position 3 of the histone.","definition_xrefs":["GOC:vk","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H4-R3 demethylation (obsolete GO:0070079)","termid":"GO:0070079"}


id: PBO:0092038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation elongation factor, glutathione S-transferase","termid":"PBO:0092038"}


id: MONDO:0017315
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Short stature-webbed neck-heart disease syndrome is characterized by short stature, intellectual deficit, facial dysmorphism, short webbed neck, skin changes and congenital heart defects. It has been reported in four Arab Bedouin sibs born to consanguineous parents.","definition_xrefs":["Orphanet:2865"],"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":"short stature-webbed neck-heart disease syndrome","secondary_identifiers":["MEDGEN:419677","SCTID:721073008","UMLS:C2930950","GARD:583","MESH:C535613"],"synonyms":[{"name":"Al Gazali Aziz Salem syndrome","type":"related"},{"name":"Al Gazali-Aziz-Salem syndrome","type":"exact"},{"name":"short stature, intellectual disability, facial dysmorphism, short webbed neck, skin changes and congenital heart disease","type":"related"},{"name":"short stature, webbed neck, heart disease","type":"related"}],"termid":"MONDO:0017315","xrefs":{"Monarch":{"xref_id":"0017315"}}}


id: MONDO:0019083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Leigh syndrome","termid":"MONDO:0009723"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005244","MONDO:0005066"],"is_obsolete":false,"name":"Leigh syndrome with cardiomyopathy","secondary_identifiers":["GARD:16685","icd11.foundation:583594497","Orphanet:70474"],"synonyms":[{"name":"Leigh disease with myopathy","type":"exact"},{"name":"cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency","type":"exact"},{"name":"cardiomyopathy with myopathy due to COX deficiency","type":"exact"}],"termid":"MONDO:0019083","xrefs":{"Monarch":{"xref_id":"0019083"}}}


id: MONDO:0008370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete reticular dystrophy of retinal pigment epithelium (obsolete MONDO:0008370)","termid":"MONDO:0008370","xrefs":{"Monarch":{"xref_id":"0008370"}}}


id: MONDO:0027653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abacavir toxicity","secondary_identifiers":["Orphanet:240841"],"termid":"MONDO:0027653","xrefs":{"Monarch":{"xref_id":"0027653"}}}


id: GO:0006389
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA-Y splicing (obsolete GO:0006389)","synonyms":[{"name":"tRNA-Y splicing","type":"exact"}],"termid":"GO:0006389"}


id: GO:1900948
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of isoprene biosynthetic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid biosynthetic process","termid":"GO:0051055"},{"relation_name":"is_a","term_name":"negative regulation of olefin biosynthetic process","termid":"GO:1900912"},{"relation_name":"is_a","term_name":"negative regulation of isoprene metabolic process","termid":"GO:1900945"},{"relation_name":"is_a","term_name":"regulation of isoprene biosynthetic process","termid":"GO:1900947"},{"relation_name":"negatively_regulates","term_name":"isoprene biosynthetic process","termid":"GO:0043612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of isoprene biosynthetic process","synonyms":[{"name":"down regulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"down regulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"down regulation of hemiterpene biosynthesis","type":"exact"},{"name":"down regulation of hemiterpene biosynthetic process","type":"exact"},{"name":"down regulation of isoprene biosynthetic process","type":"exact"},{"name":"down-regulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"down-regulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"down-regulation of hemiterpene biosynthesis","type":"exact"},{"name":"down-regulation of hemiterpene biosynthetic process","type":"exact"},{"name":"down-regulation of isoprene biosynthetic process","type":"exact"},{"name":"downregulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"downregulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"downregulation of hemiterpene biosynthesis","type":"exact"},{"name":"downregulation of hemiterpene biosynthetic process","type":"exact"},{"name":"downregulation of isoprene biosynthetic process","type":"exact"},{"name":"inhibition of 2-methyl-1,3-butadiene biosynthesis","type":"narrow"},{"name":"inhibition of 2-methyl-1,3-butadiene biosynthetic process","type":"narrow"},{"name":"inhibition of hemiterpene biosynthesis","type":"narrow"},{"name":"inhibition of hemiterpene biosynthetic process","type":"narrow"},{"name":"inhibition of isoprene biosynthetic process","type":"narrow"},{"name":"negative regulation of 2-methyl-1,3-butadiene biosynthesis","type":"exact"},{"name":"negative regulation of 2-methyl-1,3-butadiene biosynthetic process","type":"exact"},{"name":"negative regulation of hemiterpene biosynthesis","type":"exact"},{"name":"negative regulation of hemiterpene biosynthetic process","type":"exact"}],"termid":"GO:1900948"}


id: PBO:0071621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 39","termid":"PBO:0071621"}


id: PBO:0052332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1755","termid":"PBO:0052332"}


id: PBO:0079563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin associated protein 1 like","termid":"PBO:0079563"}


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: GO:0033535
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving ajugose, the hexasaccharide beta-D-fructofuranosyl alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide metabolic process","termid":"GO:0009311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"ajugose metabolic process","synonyms":[{"name":"ajugose metabolism","type":"exact"}],"termid":"GO:0033535"}


id: GO:0022856
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + sorbitol(out) = protein histidine + sorbitol phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"},{"relation_name":"is_a","term_name":"sorbitol transmembrane transporter activity","termid":"GO:0015576"}],"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:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0022857","GO:0005215","GO:0003824"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-sorbitol phosphotransferase system transporter activity","synonyms":[{"name":"sorbitol PTS transporter activity","type":"exact"}],"termid":"GO:0022856"}


id: GO:0071021
data:
  {"annotated_genes":["SJAG_02455"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[79115],"is_not":false,"summary":null,"term":"GO:0071021"}]},"cv_name":"cellular_component","definition":"A spliceosomal complex that is formed following the second splicing event and contains the spliced product, the excised intron, and three snRNPs, U5, U2 and U6.","definition_xrefs":["ISBN:0879697393","GOC:krc","ISBN:0879695897","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"U2-type spliceosomal complex","termid":"GO:0005684"},{"relation_name":"is_a","term_name":"post-spliceosomal complex","termid":"GO:0071020"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"U2-type post-spliceosomal complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"GT-AG post-spliceosomal complex","type":"narrow"},{"name":"major post-spliceosomal complex","type":"exact"},{"name":"mammalian U2-type spliceosomal complex C2","type":"narrow"},{"name":"yeast U2-type spliceosomal complex A2-3","type":"narrow"}],"termid":"GO:0071021","terms_by_termid":{"GO:0071021":null}}


id: GO:1900408
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellular response to oxidative stress.","definition_xrefs":["GOC:TermGenie","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"regulation of cellular response to oxidative stress","termid":"GO:1900407"},{"relation_name":"is_a","term_name":"negative regulation of response to oxidative stress","termid":"GO:1902883"},{"relation_name":"negatively_regulates","term_name":"cellular response to oxidative stress","termid":"GO:0034599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of cellular response to oxidative stress","synonyms":[{"name":"down regulation of adaptive response to oxidative stress","type":"narrow"},{"name":"down regulation of cellular response to oxidative stress","type":"exact"},{"name":"down-regulation of adaptive response to oxidative stress","type":"narrow"},{"name":"down-regulation of cellular response to oxidative stress","type":"exact"},{"name":"downregulation of adaptive response to oxidative stress","type":"narrow"},{"name":"downregulation of cellular response to oxidative stress","type":"exact"},{"name":"inhibition of adaptive response to oxidative stress","type":"narrow"},{"name":"inhibition of cellular response to oxidative stress","type":"narrow"},{"name":"negative regulation of adaptive response to oxidative stress","type":"narrow"}],"termid":"GO:1900408"}


id: MONDO:1012668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any von Willebrand disease that occurs in horses and is characterized by qualitative abnormalities of the glycoprotein von Willebrand factor (vWF) and moderate to severe bleeding.","definition_xrefs":["OMIA:001339-9796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Von Willebrand disease, horse","termid":"MONDO:1011614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"von Willebrand disease II, horse","termid":"MONDO:1012668","xrefs":{"Monarch":{"xref_id":"1012668"}}}


id: PBO:0044949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrofolate reductase pseudogene 5","termid":"PBO:0044949"}


id: PBO:0057508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 626","termid":"PBO:0057508"}


id: PBO:0025490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APC ubiquitin conjugating enzyme E2 Ubc4/UbcP1","termid":"PBO:0025490"}


id: GO:0009069
data:
  {"annotated_genes":["SJAG_02972","SJAG_04449","SJAG_04305","SJAG_02313","SJAG_02450","SJAG_03641","SJAG_03152","SJAG_03671","SJAG_01766","SJAG_03861","SJAG_01880","SJAG_03914","SJAG_00234","SJAG_02290","SJAG_02791","SJAG_00881","SJAG_00582","SJAG_02901"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019344"},{"annotations":[77921,60971,67692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006535"},{"annotations":[73882],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006545"},{"annotations":[73834,75094],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019264"},{"annotations":[75938,98315,79829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019464"},{"annotations":[75365,117787,72902],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009090"},{"annotations":[115932],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019450"},{"annotations":[112486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071269"},{"annotations":[102595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019280"},{"annotations":[61498,81369,118917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006564"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving amino acids of the serine family, comprising cysteine, glycine, homoserine, selenocysteine and serine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-amino acid metabolic process","termid":"GO:1901605"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00234":null,"SJAG_00582":null,"SJAG_00881":null,"SJAG_01766":null,"SJAG_01880":null,"SJAG_02290":null,"SJAG_02313":null,"SJAG_02450":null,"SJAG_02791":null,"SJAG_02901":null,"SJAG_02972":null,"SJAG_03152":null,"SJAG_03641":null,"SJAG_03671":null,"SJAG_03861":null,"SJAG_03914":null,"SJAG_04305":null,"SJAG_04449":null},"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:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"serine family amino acid metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"serine family amino acid metabolism","type":"exact"}],"termid":"GO:0009069","terms_by_termid":{"GO:0006535":null,"GO:0006545":null,"GO:0006564":null,"GO:0009090":null,"GO:0019264":null,"GO:0019280":null,"GO:0019344":null,"GO:0019450":null,"GO:0019464":null,"GO:0071269":null}}


id: PBO:0062992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase C and casein kinase substrate in neurons 1","termid":"PBO:0062992"}


id: MONDO:0859225
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with or without variable movement or behavioral abnormalities","secondary_identifiers":["MEDGEN:1802087","OMIM:619725","UMLS:C5676908"],"termid":"MONDO:0859225","xrefs":{"Monarch":{"xref_id":"0859225"}}}


id: PATO:0001977
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's having at least one salient angle on the margin.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angular","synonyms":[{"name":"angulate","type":"exact"}],"termid":"PATO:0001977"}


id: GO:1902567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of eosinophil activation.","definition_xrefs":["GOC:TermGenie","PMID:16254138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte activation","termid":"GO:0002695"},{"relation_name":"is_a","term_name":"regulation of eosinophil activation","termid":"GO:1902566"},{"relation_name":"negatively_regulates","term_name":"eosinophil activation","termid":"GO:0043307"}],"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 eosinophil activation","synonyms":[{"name":"down regulation of eosinophil activation","type":"exact"},{"name":"down-regulation of eosinophil activation","type":"exact"},{"name":"downregulation of eosinophil activation","type":"exact"},{"name":"inhibition of eosinophil activation","type":"narrow"}],"termid":"GO:1902567"}


id: PBO:0003654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-SWIM","termid":"PBO:0003654"}


id: MONDO:1010425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Phelan-McDermid syndrome that occurs in crab-eating macaque.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Phelan-McDermid syndrome, non-human animal","termid":"MONDO:1010006"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phelan-McDermid syndrome, crab-eating macaque","secondary_identifiers":["OMIA:002402-9541"],"termid":"MONDO:1010425","xrefs":{"Monarch":{"xref_id":"1010425"}}}


id: GO:1990076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any cell wall polysaccharide catabolic process that is involved in abscission.","definition_xrefs":["GOC:TermGenie","PMID:23479623"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell wall polysaccharide catabolic process","termid":"GO:0044347"},{"relation_name":"part_of","term_name":"abscission","termid":"GO:0009838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0071554"],"is_obsolete":false,"name":"cell wall polysaccharide catabolic process involved in abscission","termid":"GO:1990076"}


id: PBO:0065957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD23 homolog A, nucleotide excision repair protein","termid":"PBO:0065957"}


id: PBO:0087379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sterol-binding protein; has a probable role in retrograde transport of sterols from the plasma membrane to the ER; contains two StART-like domains that bind sterols and a GRAM domain; co-localizes to puncta in the cortical ER with Sip3p; one of six StART-like domain-containing proteins in yeast that may be involved in sterol transfer between intracellular membranes; conserved across eukaryotes","termid":"PBO:0087379"}


id: GO:0048208
data:
  {"annotated_genes":["SJAG_00906","SJAG_04615"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73227,78111],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0003400"}]},"cv_name":"biological_process","definition":"The addition of COPII proteins and adaptor proteins to ER membranes during the formation of transport vesicles, forming a vesicle coat.","definition_xrefs":["GOC:dph","GOC:ascb_2009","GOC:jid","GOC:mah","PMID:10219233","GOC:tb","ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle coating","termid":"GO:0006901"},{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"vesicle targeting, rough ER to cis-Golgi","termid":"GO:0048207"},{"relation_name":"part_of","term_name":"COPII-coated vesicle budding","termid":"GO:0090114"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00906":null,"SJAG_04615":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150","GO:0006810","GO:0061024","GO:0016192"],"is_obsolete":false,"name":"COPII vesicle coating","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-204005"],"synonyms":[{"name":"COPII coating of ER-derived vesicle","type":"exact"},{"name":"COPII vesicle coat assembly","type":"exact"},{"name":"COPII vesicle coat formation","type":"exact"}],"termid":"GO:0048208","terms_by_termid":{"GO:0003400":null}}


id: PBO:0076163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfatase 1","termid":"PBO:0076163"}


id: PBO:0041620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium binding protein 7","termid":"PBO:0041620"}


id: MONDO:0004559
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A variant of malignant peripheral nerve sheath tumor characterized by the presence of glandular epithelium.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant peripheral nerve sheath tumor","termid":"MONDO:0017827"}],"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":"malignant glandular tumor of peripheral nerve sheath","secondary_identifiers":["MEDGEN:232558","ICD9:171.9","NCIT:C6560","DOID:8420","UMLS:C1333821","SCTID:699659007"],"synonyms":[{"name":"glandular MPNST","type":"exact"},{"name":"glandular malignant peripheral nerve sheath tumor","type":"exact"},{"name":"glandular malignant peripheral nerve sheath tumour","type":"exact"},{"name":"malignant glandular neoplasm of peripheral nerve sheath","type":"exact"},{"name":"malignant glandular neoplasm of the peripheral nerve sheath","type":"exact"},{"name":"malignant glandular peripheral nerve sheath neoplasm","type":"exact"},{"name":"malignant glandular peripheral nerve sheath tumor","type":"exact"},{"name":"malignant glandular peripheral nerve sheath tumour","type":"exact"},{"name":"malignant glandular schwannoma","type":"exact"},{"name":"malignant glandular tumor of peripheral nerve sheath","type":"exact"},{"name":"malignant glandular tumor of the peripheral nerve sheath","type":"exact"},{"name":"malignant glandular tumour of the peripheral nerve sheath","type":"exact"}],"termid":"MONDO:0004559","xrefs":{"Monarch":{"xref_id":"0004559"}}}


id: GO:0072023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the thick ascending limb over time, from its formation to the mature structure. The thick ascending limb is the last part of the loop of Henle. Its thick, mitochondria-rich epithelium characterizes the outer medulla, and is responsible for very avid active salt transport. At the macula densa, the thick ascending limb connects to the distal convoluted tubule.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron tubule development","termid":"GO:0072080"},{"relation_name":"part_of","term_name":"distal tubule development","termid":"GO:0072017"}],"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":"thick ascending limb development","secondary_identifiers":["GO:0072026"],"synonyms":[{"name":"TAL development","type":"exact"}],"termid":"GO:0072023"}


id: MONDO:0020639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chromosomal abnormality consisting of the absence of one chromosome from the normal diploid number.","definition_xrefs":["NCIT:C3239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aneuploidy","termid":"MONDO:0700064"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monosomy","secondary_identifiers":["MESH:D009006","MEDGEN:6432","UMLS:C0026499"],"termid":"MONDO:0020639","xrefs":{"Monarch":{"xref_id":"0020639"}}}


id: GO:0070762
data:
  {"annotated_genes":["SJAG_01834","SJAG_03200"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[75767,121158],"is_not":false,"summary":null,"term":"GO:0070762"}]},"cv_name":"cellular_component","definition":"A subcomplex of the nuclear pore complex (NPC) that spans the nuclear membrane and anchors the NPC to the nuclear envelope. In S. cerevisiae, the transmembrane ring is composed of Pom152p, Pom34p, and Ndc1p. In vertebrates, it is composed of Gp210, Ndc1, and Pom121. Components are arranged in 8-fold symmetrical 'spokes' around the central transport channel. A single 'spoke', can be isolated and is sometime referred to as the Ndc1 complex.","definition_xrefs":["GOC:dgf","PMID:18046406","PMID:19524430","PMID:20947011","PMID:22419078"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear pore","termid":"GO:0005643"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01834":null,"SJAG_03200":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005643"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005643","GO:0005634"],"is_obsolete":false,"name":"nuclear pore transmembrane ring","references_by_uniquename":{"GO_REF:0000033":null,"PMID:21733045":null},"synonyms":[{"name":"NDC1 complex","type":"exact"},{"name":"NDC1 subcomplex","type":"exact"}],"termid":"GO:0070762","terms_by_termid":{"GO:0070762":null}}


id: SO:0000987
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A quality of a nucleotide polymer that has a 3'-terminal residue and a 5'-terminal residue.","definition_xrefs":["SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"topology_attribute","termid":"SO:0000986"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"linear","synonyms":[{"name":"two-ended","type":"related"}],"termid":"SO:0000987"}


id: MONDO:0004833
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the thick tissue on the bottom of the foot (plantar fascia) causing heel pain. The plantar fascia (also called plantar aponeurosis) are bands of fibrous tissue extending from the calcaneal tuberosity to the toes. The etiology of plantar fasciitis remains controversial but is likely to involve a biomechanical imbalance. Though often presenting along with heel spur, they do not appear to be causally related.","definition_xrefs":["MESH:D036981"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fasciitis","termid":"MONDO:0004830"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plantar fasciitis","secondary_identifiers":["DOID:9600","MEDGEN:56201","icd11.foundation:254630809","SCTID:202882003","UMLS:C0149756"],"termid":"MONDO:0004833","xrefs":{"Monarch":{"xref_id":"0004833"}}}


id: PBO:0040861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BLVRB pseudogene 1","termid":"PBO:0040861"}


id: GO:1905763
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a MTREC complex.","definition_xrefs":["PMID:26942678","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"MTREC complex binding","synonyms":[{"name":"Mtl1-Red1 core complex binding","type":"exact"},{"name":"NURS complex binding","type":"exact"},{"name":"PAXT complex binding","type":"exact"}],"termid":"GO:1905763"}


id: PBO:0054535
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 1935","termid":"PBO:0054535"}


id: PBO:0058597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6729","termid":"PBO:0058597"}


id: GO:0097397
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-32 stimulus.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"},{"relation_name":"is_a","term_name":"response to interleukin-32","termid":"GO:0097395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to interleukin-32","synonyms":[{"name":"cellular response to IL-32","type":"exact"}],"termid":"GO:0097397"}


id: GO:0043758
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + acetate + CoA = ADP + phosphate + acetyl-CoA.","definition_xrefs":["RHEA:15081"],"direct_ancestors":[{"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016874"],"is_obsolete":false,"name":"acetate-CoA ligase (ADP-forming) activity","secondary_identifiers":["GO:0043762","EC:6.2.1.13","MetaCyc:ACETATE--COA-LIGASE-ADP-FORMING-RXN"],"synonyms":[{"name":"acetate thiokinase activity","type":"broad"},{"name":"acetate--CoA ligase (ADP-forming) activity","type":"exact"},{"name":"acetate:CoA ligase (ADP-forming)","type":"related"},{"name":"acetyl coenzyme A synthetase (adenosine diphosphate-forming)","type":"exact"},{"name":"acetyl-CoA synthetase (ADP-forming) activity","type":"related"},{"name":"aryl-CoA synthetase (ADP-forming) activity","type":"related"}],"termid":"GO:0043758"}


id: GO:1900822
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ergot alkaloid biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"ergot alkaloid biosynthetic process","termid":"GO:0035837"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"regulation of ergot alkaloid biosynthetic process","synonyms":[{"name":"regulation of ergot alkaloid anabolism","type":"exact"},{"name":"regulation of ergot alkaloid biosynthesis","type":"exact"},{"name":"regulation of ergot alkaloid formation","type":"exact"},{"name":"regulation of ergot alkaloid synthesis","type":"exact"}],"termid":"GO:1900822"}


id: GO:0062236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized structural and/or functional features of an ionocyte. Ionocytes are specialized epithelial cells that contribute to osmotic homeostasis.","definition_xrefs":["PMID:17555741"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell differentiation","termid":"GO:0030855"}],"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":"ionocyte differentiation","termid":"GO:0062236"}


id: PBO:0013070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxin-2 homolog","termid":"PBO:0013070"}


id: GO:0019651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The anaerobic chemical reactions and pathways resulting in the breakdown of citrate to diacetyl, yielding energy in the form of ATP.","definition_xrefs":["MetaCyc:P126-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"citrate metabolic process","termid":"GO:0006101"},{"relation_name":"is_a","term_name":"non-glycolytic fermentation","termid":"GO:0019662"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"tricarboxylic acid catabolic process","termid":"GO:0072352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0044281","GO:0006091","GO:0008150"],"is_obsolete":false,"name":"citrate catabolic process to diacetyl","synonyms":[{"name":"citrate fermentation to diacetyl","type":"exact"},{"name":"diacetyl fermentation","type":"exact"}],"termid":"GO:0019651"}


id: MONDO:0000737
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete megalocornea (obsolete MONDO:0000737)","termid":"MONDO:0000737","xrefs":{"Monarch":{"xref_id":"0000737"}}}


id: GO:0019476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of D-lysine, the D-enantiomer of lysine; i.e. (2R)-2,6-diaminohexanoic acid.","definition_xrefs":["GOC:mah","GOC:jsg","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysine catabolic process","termid":"GO:0006554"},{"relation_name":"is_a","term_name":"D-amino acid catabolic process","termid":"GO:0019478"},{"relation_name":"is_a","term_name":"D-lysine metabolic process","termid":"GO:0046441"}],"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:0006520"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"D-lysine catabolic process","synonyms":[{"name":"D-lysine breakdown","type":"exact"},{"name":"D-lysine catabolism","type":"exact"},{"name":"D-lysine degradation","type":"exact"}],"termid":"GO:0019476"}


id: GO:0102747
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + chlorophyllide a(1-) + 2-trans,6-trans,10-trans-geranylgeranyl diphosphate(3-) = geranylgeranyl-chlorophyll a + diphosphoric acid.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete chlorophyllide-a:geranyl-geranyl diphosphate geranyl-geranyl transferase activity (obsolete GO:0102747)","termid":"GO:0102747"}


id: FYECO:0000273
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in medium containing salts, water, a nitrogen source but no glucose.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucose MM, no glucose","termid":"FYECO:0000273"}


id: FYPO:0002960
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of one or more RNAs that are normally expressed during the meiotic cell cycle, and that contain determinant of selective removal (DSR) sequences, measured in a cell is higher than normal (i.e. higher than observed in wild-type cells during vegetative growth).","definition_xrefs":["PMID:23980030","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of meiotic gene mRNA during vegetative growth","termid":"FYPO:0002173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0006551","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"increased level of DSR-containing meiotic gene mRNA during vegetative growth","synonyms":[{"name":"increased DSR-containing meiotic gene mRNA accumulation during vegetative growth","type":"related"},{"name":"increased level of DSR-containing meiosis gene mRNA during vegetative growth","type":"exact"},{"name":"increased level of DSR-containing meiotic cell cycle gene mRNA during vegetative growth","type":"related"},{"name":"increased level of DSR-containing meiotic gene RNA during vegetative growth","type":"exact"},{"name":"increased level of DSR-containing meiotic gene mRNA during mitotic cell cycle","type":"related"},{"name":"increased level of DSR-containing meiotic gene transcripts during vegetative growth","type":"exact"},{"name":"increased level of DSR-containing meiotic nuclear division gene mRNA during vegetative growth","type":"exact"}],"termid":"FYPO:0002960"}


id: PBO:0083322
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 ORF SAP1/YER047C","termid":"PBO:0083322"}


id: PATO:0001398
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A cellular quality inhering in a bearer by virtue of the bearer's having the ability to go through numerous cycles of cell division while maintaining the undifferentiated state.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proliferative","termid":"PATO:0002102"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"self-renewal","termid":"PATO:0001398"}


id: SO:0000233
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript which has undergone the necessary modifications, if any, for its function. In eukaryotes this includes, for example, processing of introns, cleavage, base modification, and modifications to the 5' and/or the 3' ends, other than addition of bases. In bacteria functional mRNAs are usually not modified.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"primary_transcript","termid":"SO:0000185"},{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mature_transcript","secondary_identifiers":["http://en.wikipedia.org/wiki/Mature_transcript"],"synonyms":[{"name":"mature transcript","type":"exact"}],"termid":"SO:0000233"}


id: PBO:0005622
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homotrimer","termid":"PBO:0005622"}


id: MOD:01166
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an amino acid residue and 5'-phosphouridine through either a phosphodiester or a phosphoramide bond.","definition_xrefs":["Unimod:417","DeltaMass:292"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide or nucleic acid modified residue","termid":"MOD:00701"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridylated residue","synonyms":[{"name":"5'phos Uridinyl","type":"exact"},{"name":"PhosphoUridine","type":"related"},{"name":"uridine phosphodiester","type":"related"}],"termid":"MOD:01166"}


id: GO:0034381
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a lipoprotein particle is removed from the blood via receptor-mediated endocytosis and its constituent parts degraded.","definition_xrefs":["GOC:mah","GOC:BHF","GOC:dph","GOC:tb","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"regulation of plasma lipoprotein particle levels","termid":"GO:0097006"}],"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 lipoprotein particle clearance","secondary_identifiers":["Reactome:R-HSA-8964043"],"synonyms":[{"name":"lipoprotein particle clearance","type":"exact"}],"termid":"GO:0034381"}


id: PBO:0071699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL38 pseudogene 5","termid":"PBO:0071699"}


id: PBO:0050377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 1","termid":"PBO:0050377"}


id: PATO:0001839
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A fluid flow that is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"fluid flow rate","termid":"PATO:0002243"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased fluid flow","synonyms":[{"name":"high flow","type":"exact"}],"termid":"PATO:0001839"}


id: GO:0160060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A homeostatic process in which the drive for sleep increases sleep propensity with prolonged wakefulness.","definition_xrefs":["PMID:30509635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal-level homeostasis","termid":"GO:0048871"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"sleep homeostasis","termid":"GO:0160060"}


id: MONDO:1012108
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrophic neuropathy, non-human animal","termid":"MONDO:1011844"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrophic neuropathy, dog","secondary_identifiers":["OMIA:000518-9615"],"termid":"MONDO:1012108","xrefs":{"Monarch":{"xref_id":"1012108"}}}


id: MONDO:0020169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disorder with ptosis (obsolete MONDO:0020169)","secondary_identifiers":["Orphanet:98578"],"termid":"MONDO:0020169","xrefs":{"Monarch":{"xref_id":"0020169"}}}


id: PBO:0111824
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHCH domain","termid":"PBO:0111824"}


id: PR:000045537
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GTP-binding nuclear protein spi1 that is encoded in the genome of Schizosaccharomyces pombe.","definition_xrefs":["PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GTP-binding nuclear protein spi1","termid":"PR:000027715"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-binding nuclear protein spi1 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC1289.03c","synonyms":[{"name":"Spom-spi1","type":"exact"}],"termid":"PR:000045537"}


id: PBO:0091904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf element Wtf6 (frameshifted)","termid":"PBO:0091904"}


id: GO:2000845
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of testosterone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid transport","termid":"GO:0032370"},{"relation_name":"is_a","term_name":"positive regulation of hormone secretion","termid":"GO:0046887"},{"relation_name":"is_a","term_name":"regulation of testosterone secretion","termid":"GO:2000843"},{"relation_name":"positively_regulates","term_name":"testosterone secretion","termid":"GO:0035936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of testosterone secretion","termid":"GO:2000845"}


id: GO:0000398
data:
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id: PBO:0011099
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id: MONDO:0957432
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id: GO:0170033
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acid metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"synonyms":[{"name":"L-alpha-amino acid metabolism","type":"exact"},{"name":"L-amino acid metabolism","type":"exact"}],"termid":"GO:0170033","terms_by_termid":{"GO:0000053":null,"GO:0000105":null,"GO:0000162":null,"GO:0006528":null,"GO:0006532":null,"GO:0006533":null,"GO:0006535":null,"GO:0006536":null,"GO:0006538":null,"GO:0006541":null,"GO:0006542":null,"GO:0006551":null,"GO:0006555":null,"GO:0006564":null,"GO:0006567":null,"GO:0006571":null,"GO:0006574":null,"GO:0009086":null,"GO:0009088":null,"GO:0009094":null,"GO:0009098":null,"GO:0009099":null,"GO:0010121":null,"GO:0010133":null,"GO:0019264":null,"GO:0019280":null,"GO:0019284":null,"GO:0019450":null,"GO:0019509":null,"GO:0019544":null,"GO:0019676":null,"GO:0019878":null,"GO:0033387":null,"GO:0042450":null,"GO:0042852":null,"GO:0042853":null,"GO:0055129":null,"GO:0070981":null,"GO:0071266":null,"GO:0071269":null,"GO:0097054":null,"GO:1901705":null}}


id: GO:2000713
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of maintenance of meiotic sister chromatid cohesion along the chromosome arms.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of maintenance of meiotic sister chromatid cohesion, arms (obsolete GO:2000713)","synonyms":[{"name":"negative regulation of maintenance of meiotic sister chromatin cohesion along arms","type":"exact"},{"name":"negative regulation of maintenance of sister chromatin cohesion along arms at meiosis I","type":"exact"}],"termid":"GO:2000713"}


id: MONDO:0009543
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Prominent glabella B microcephaly B hypogenitalism is a very rare syndrome described in two sibs and characterized by prenatal onset of growth deficiency, microcephaly, hypoplastic genitalia, and birth onset of convulsions.","definition_xrefs":["Orphanet:2083"],"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":"prominent glabella-microcephaly-hypogenitalism syndrome","secondary_identifiers":["UMLS:C0796024","MEDGEN:162900","OMIM:247990","GARD:144","MESH:C537714"],"synonyms":[{"name":"Mac Dermot Winter syndrome","type":"related"},{"name":"MacDermot-Winter syndrome","type":"exact"},{"name":"prominent glabella microcephaly hypogenitalism","type":"related"}],"termid":"MONDO:0009543","xrefs":{"Monarch":{"xref_id":"0009543"}}}


id: PBO:0083412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the essential gene AAR2/YBL074C","termid":"PBO:0083412"}


id: GO:0004941
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with epinephrine or norepinephrine to initiate a change in cell activity via activation of a G protein, with pharmacological characteristics of beta2-adrenergic receptors.","definition_xrefs":["GOC:mah","IUPHAR_GPCR:1274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-adrenergic receptor activity","termid":"GO:0004939"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"beta2-adrenergic receptor activity","synonyms":[{"name":"beta2 adrenoceptor","type":"exact"}],"termid":"GO:0004941"}


id: PBO:0054928
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 2342","termid":"PBO:0054928"}


id: MONDO:1012287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive ataxia, non-human animal","termid":"MONDO:1011633"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive ataxia, dog","secondary_identifiers":["OMIA:001091-9615"],"termid":"MONDO:1012287","xrefs":{"Monarch":{"xref_id":"1012287"}}}


id: GO:0019460
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of glutamine into other compounds, including fumarate.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete glutamine catabolic process to fumarate (obsolete GO:0019460)","synonyms":[{"name":"glutamate catabolic process to fumarate","type":"narrow"},{"name":"glutamine breakdown to fumarate","type":"exact"},{"name":"glutamine degradation to fumarate","type":"exact"}],"termid":"GO:0019460"}


id: PBO:0036256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic ER membrane protein implicated in cholesterol metabolism in human (predicted)","termid":"PBO:0036256"}


id: MONDO:0859317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"pseudohypoaldosteronism type 1","termid":"MONDO:0019161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005240"],"is_obsolete":false,"name":"pseudohypoaldosteronism, type IB2, autosomal recessive","secondary_identifiers":["UMLS:C5774255","OMIM:620125","MEDGEN:1824028"],"termid":"MONDO:0859317","xrefs":{"Monarch":{"xref_id":"0859317"}}}


id: GO:0140453
data:
  {"annotated_genes":["SJAG_01664","SJAG_04666","SJAG_04055","SJAG_01186","SJAG_04567","SJAG_03794","SJAG_02013","SJAG_04187","SJAG_03164","SJAG_02381","SJAG_00436","SJAG_03815","SJAG_01529"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[60639,92682,94297,96933,98444,102632,106140,106945,111977,111978,117501,118723,120610],"is_not":false,"summary":null,"term":"GO:0140453"}]},"cv_name":"cellular_component","definition":"Reversible aggregate of misfolded proteins and chaperones formed to shield thermosensitive proteins from degradation until conditions allow disaggregation and refolding.","definition_xrefs":["PMID:32075773"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00436":null,"SJAG_01186":null,"SJAG_01529":null,"SJAG_01664":null,"SJAG_02013":null,"SJAG_02381":null,"SJAG_03164":null,"SJAG_03794":null,"SJAG_03815":null,"SJAG_04055":null,"SJAG_04187":null,"SJAG_04567":null,"SJAG_04666":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"protein aggregate center","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"PAC","type":"broad"},{"name":"protein aggregate centre","type":"exact"}],"termid":"GO:0140453","terms_by_termid":{"GO:0140453":null}}


id: PBO:0057388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548BC","termid":"PBO:0057388"}


id: FYPO:0001752
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of homocitrate synthase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal homocitrate synthase activity","termid":"FYPO:0001750"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000654","FYPO:0000661","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"decreased homocitrate synthase activity","synonyms":[{"name":"reduced homocitrate synthase activity","type":"exact"}],"termid":"FYPO:0001752"}


id: PBO:0054381
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 1777","termid":"PBO:0054381"}


id: MONDO:0008344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary edema of mountaineers, susceptibility to","secondary_identifiers":["UMLS:C0340552","ICD9:416.8","ICD9:993.2","MEDGEN:83314","MESH:C535833","OMIM:178400","SCTID:233954004"],"synonyms":[{"name":"HAPH","type":"related"},{"name":"high altitude pulmonary hypertension","type":"related"},{"name":"pulmonary edema of mountaineers","type":"related"},{"name":"pulmonary edema of mountaineers, susceptibility to","type":"exact"},{"name":"pulmonary oedema of mountaineers","type":"related"}],"termid":"MONDO:0008344","xrefs":{"Monarch":{"xref_id":"0008344"}}}


id: MONDO:0009019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare subtype of posterior corneal dystrophy characterized by a diffuse ground-glass appearance of the corneas and marked corneal thickening from birth with nystagmus, and blurred vision.","definition_xrefs":["Orphanet:293603"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corneal endothelial dystrophy","termid":"MONDO:0000766"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"posterior corneal dystrophy","termid":"MONDO:0020214"}],"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":"congenital hereditary endothelial dystrophy of cornea","secondary_identifiers":["MESH:C536439","OMIM:217700","GARD:6196","MEDGEN:387857","UMLS:C1857569","DOID:0060649"],"synonyms":[{"name":"CHED","type":"exact"},{"name":"CHED2","type":"exact"},{"name":"CHED2, formerly","type":"related"},{"name":"CHEDII","type":"exact"},{"name":"autosomal recessive CHED","type":"exact"},{"name":"autosomal recessive congenital hereditary endothelial dystrophy","type":"exact"},{"name":"congenital hereditary endothelial dystrophy of cornea","type":"exact"},{"name":"congenital hereditary endothelial dystrophy of the cornea","type":"related"},{"name":"congenital hereditary endothelial dystrophy type 2","type":"exact"},{"name":"congenital hereditary endothelial dystrophy type II","type":"related"},{"name":"corneal dystrophy, congenital hereditary endothelial","type":"related"},{"name":"corneal endothelial dystrophy","type":"related"},{"name":"corneal endothelial dystrophy 2","type":"related"},{"name":"corneal endothelial dystrophy 2, autosomal recessive","type":"related"},{"name":"corneal endothelial dystrophy 2, autosomal recessive, formerly","type":"related"},{"name":"corneal endothelial dystrophy type 2","type":"related"},{"name":"corneal endothelial dystrophy, autosomal recessive","type":"exact"},{"name":"infantile hereditary endothelial dystrophy","type":"exact"}],"termid":"MONDO:0009019","xrefs":{"Monarch":{"xref_id":"0009019"}}}


id: MONDO:0700209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Strongylida infectious disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic disease, non-human animal","termid":"MONDO:0024969"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Strongylida infectious disease, non-human animal","termid":"MONDO:0700209","xrefs":{"Monarch":{"xref_id":"0700209"}}}


id: PBO:0000995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-methylthioribulose-1-phosphate dehydratase, adducin (predicted)","termid":"PBO:0000995"}


id: GO:0006337
data:
  {"annotated_genes":["SJAG_02314","SJAG_04038","SJAG_01653"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91935,98996,118911],"is_not":false,"summary":null,"term":"GO:0006337"}]},"cv_name":"biological_process","definition":"The controlled breakdown of nucleosomes, the beadlike structural units of eukaryotic chromatin composed of histones and DNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex disassembly","termid":"GO:0032986"},{"relation_name":"is_a","term_name":"nucleosome organization","termid":"GO:0034728"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01653":null,"SJAG_02314":null,"SJAG_04038":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006325","GO:0008150"],"is_obsolete":false,"name":"nucleosome disassembly","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0006337","terms_by_termid":{"GO:0006337":null}}


id: PBO:0046821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FA core complex associated protein 100","termid":"PBO:0046821"}


id: PBO:0070215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 147 pseudogene","termid":"PBO:0070215"}


id: MOD:01089
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"xanthyl","synonyms":[{"name":"Xan","type":"exact"}],"termid":"MOD:01089"}


id: PBO:0036197
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H4-K20_monomethylation_during_vegetative_growth","termid":"PBO:0036197"}


id: GO:0106348
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a adenosine in U2 snRNA + S-adenosyl-L-methionine = an N6-methyl-adenosine in U2 snRNA + S-adenosyl-L-homocysteine + H+.","definition_xrefs":["PMID:32637152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA methyltransferase activity","termid":"GO:0106346"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016741","GO:0003824","GO:0016740","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"U2 snRNA adenosine m6 methyltransferase activity","termid":"GO:0106348"}


id: PBO:0054405
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 1801","termid":"PBO:0054405"}


id: MOD:00233
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-lysine residue and 5'-phosphoguanosine through a phosphoramide ester bond to form N6-(phospho-5'-guanosine)-L-lysine.","definition_xrefs":["PubMed:6264433","DeltaMass:304","PubMed:6092377","RESID:AA0228","Unimod:413#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"},{"relation_name":"is_a","term_name":"guanylated residue","termid":"MOD:01163"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N6-(phospho-5'-guanosine)-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-(5'-guanosine phosphonamino)hexanoic acid","type":"exact"},{"name":"5'-guanylic-N6-L-lysine","type":"exact"},{"name":"5'phos Guanosyl","type":"exact"},{"name":"ACT_SITE N6-GMP-lysine intermediate","type":"exact"},{"name":"L-lysine monoanhydride with 5'-guanylic acid","type":"exact"},{"name":"N(zeta)-5'-guanylic-lysine","type":"exact"},{"name":"N6-(5'-guanylyl)-lysine","type":"exact"},{"name":"N6-(phospho-5'-guanosine)-L-lysine","type":"exact"},{"name":"N6-L-lysine 5'-guanosine phosphoramidester","type":"exact"},{"name":"N6GMPLys","type":"exact"},{"name":"Phosphoguanosine","type":"related"},{"name":"epsilon-5'-guanylic-L-lysine","type":"exact"},{"name":"lysine guanosine-5'-monophosphate","type":"exact"},{"name":"phospho-guanosine","type":"related"}],"termid":"MOD:00233"}


id: FYPO:0006454
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the meiotic spindle is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"},{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton","termid":"FYPO:0004090"},{"relation_name":"is_a","term_name":"abnormal protein localization to spindle","termid":"FYPO:0007863"}],"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"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein localization to meiotic spindle","synonyms":[{"name":"abnormal protein localisation to meiotic spindle","type":"exact"},{"name":"abnormal protein localization to spindle during meiosis","type":"exact"}],"termid":"FYPO:0006454"}


id: PBO:0071275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL24 pseudogene 9","termid":"PBO:0071275"}


id: PBO:0084185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Histone demethylase and transcription factor; regulates genes during nutrient limitation; activity modulated by proteasome-mediated proteolysis; has JmjC and JmjN domain in N-terminus that interact, promoting stability and proper transcriptional activity; contains two transactivating domains downstream of Jmj domains and a C-terminal DNA binding domain; relocalizes to the cytosol in response to hypoxia; GIS1 has a paralog, RPH1, that arose from the whole genome duplication","termid":"PBO:0084185"}


id: GO:0140373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the addition of one or more ubiquitin groups to a lysine residue at position 14 of the histone.","definition_xrefs":["PMID:31468675","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K14 ubiquitination (obsolete GO:0140373)","synonyms":[{"name":"histone H3 ubiquitination at K14","type":"exact"},{"name":"histone H3-K14 ubiquitylation","type":"exact"},{"name":"histone H3K14 ubiquitination","type":"exact"}],"termid":"GO:0140373"}


id: PBO:0111352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small subunit processome, U3 snoRNP-associated protein Utp13","termid":"PBO:0111352"}


id: GO:0032623
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-2 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"interleukin-2 production","secondary_identifiers":["GO:0070970","GO:0042094"],"synonyms":[{"name":"IL-2 production","type":"exact"},{"name":"interleukin-2 biosynthetic process","type":"narrow"},{"name":"interleukin-2 secretion","type":"narrow"}],"termid":"GO:0032623"}


id: PBO:0064969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 25","termid":"PBO:0064969"}


id: GO:0018230
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The covalent attachment of a palmitoyl group to a sulfur (S) atom within a cysteine residue to form peptidyl-S-palmitoyl-L-cysteine.","definition_xrefs":["RESID:AA0106"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine","termid":"GO:0018231"},{"relation_name":"is_a","term_name":"protein palmitoylation","termid":"GO:0018345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0042158"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0042158"],"is_obsolete":false,"name":"peptidyl-L-cysteine S-palmitoylation","synonyms":[{"name":"peptidyl-S-palmitoyl-L-cysteine anabolism from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-palmitoyl-L-cysteine biosynthetic process from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-palmitoyl-L-cysteine formation from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-S-palmitoyl-L-cysteine synthesis from peptidyl-cysteine","type":"exact"},{"name":"peptidyl-cysteine S-palmitoylation","type":"exact"}],"termid":"GO:0018230"}


id: GO:0046019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involving pheromones that modulates the frequency, rate or extent or transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:txnOH","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter by pheromones (obsolete GO:0046019)","synonyms":[{"name":"regulation of transcription from Pol II promoter by pheromones","type":"exact"}],"termid":"GO:0046019"}


id: FYPO:0002612
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 is normal at subtelomeric regions. All histone H2A phosphorylation may be assayed, or phosphorylation of specific sites on histone H2A may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H2A phosphorylation during vegetative growth","termid":"FYPO:0002601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal histone H2A phosphorylation at subtelomeric heterochromatin during vegetative growth","synonyms":[{"name":"normal histone H2A phosphorylation at subtelomere during vegetative growth","type":"exact"},{"name":"normal histone H2A phosphorylation at subtelomeric heterochromatin during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002612"}


id: FYPO:0008055
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a Glc2Man9GlcNAc2 oligosaccharide glucosidase activity is decreased.","definition_xrefs":["PMID:23609449"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000652","FYPO:0000707","FYPO:0000661","FYPO:0001985"],"is_obsolete":false,"name":"decreased Glc2Man9GlcNAc2 oligosaccharide glucosidase activity","termid":"FYPO:0008055"}


id: FYPO:0003839
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 nucleolus is abnormal during mitotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"},{"relation_name":"is_a","term_name":"abnormal protein localization to nucleus","termid":"FYPO:0002956"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization to nucleolus during mitosis","synonyms":[{"name":"abnormal protein localisation to nucleolus during mitosis","type":"exact"},{"name":"abnormal protein localization to nucleolus during mitosis during vegetative growth","type":"exact"},{"name":"abnormal protein localization to nucleolus during mitotic M phase","type":"related"}],"termid":"FYPO:0003839"}


id: GO:0046450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving dethiobiotin, a derivative of biotin formed by replacing the sulfur atom by two hydrogen atoms.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"dethiobiotin metabolic process","synonyms":[{"name":"desthiobiotin metabolic process","type":"exact"},{"name":"desthiobiotin metabolism","type":"exact"},{"name":"dethiobiotin metabolism","type":"exact"}],"termid":"GO:0046450"}


id: PBO:0057838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3154","termid":"PBO:0057838"}


id: PBO:0085081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear decapping endonuclease; targets mRNAs with unmethylated 7-methylguanosine cap structures and 5'-triphosphates; binds to and stabilizes the exoribonuclease Rat1p; required for pre-rRNA processing; involved in an early step of decapping nicotinamide adenine dinucleotide (NAD) capped nuclear NAD-RNAs; relocalizes to the cytosol in response to hypoxia; homologous to human DOM3Z","termid":"PBO:0085081"}


id: GO:0002027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency or rate of heart contraction.","definition_xrefs":["GOC:dph","GOC:tb","PMID:10358008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart contraction","termid":"GO:0008016"},{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"}],"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 heart rate","synonyms":[{"name":"cardiac chronotropy","type":"exact"},{"name":"regulation of heart contraction rate","type":"exact"},{"name":"regulation of rate of heart contraction","type":"exact"}],"termid":"GO:0002027"}


id: PBO:0073606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shootin 1","termid":"PBO:0073606"}


id: PBO:0067314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 400, pseudogene","termid":"PBO:0067314"}


id: GO:0097211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a gonadotropin-releasing hormone stimulus. Gonadotropin-releasing hormone (GnRH) is a peptide hormone responsible for the release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) from the anterior pituitary. GnRH is synthesized and released by the hypothalamus.","definition_xrefs":["PMID:15976007","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to peptide hormone stimulus","termid":"GO:0071375"},{"relation_name":"is_a","term_name":"response to gonadotropin-releasing hormone","termid":"GO:0097210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to gonadotropin-releasing hormone","synonyms":[{"name":"cellular response to GnRH","type":"exact"},{"name":"cellular response to gonadotrophin-releasing hormone","type":"exact"}],"termid":"GO:0097211"}


id: GO:0097305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an alcohol stimulus.","definition_xrefs":["GOC:pr","PMID:24014527"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to alcohol","secondary_identifiers":["GO:1990335"],"synonyms":[{"name":"process resulting in tolerance to alcohol","type":"narrow"}],"termid":"GO:0097305"}


id: GO:0071093
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha5-beta1 integrin complex bound to fibronectin and tissue transglutaminase.","definition_xrefs":["PMID:10684262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"alpha5-beta1 integrin-fibronectin-tissue transglutaminase complex","synonyms":[{"name":"ITGA5-ITGB1-FN1-TGM2 complex","type":"narrow"}],"termid":"GO:0071093"}


id: PBO:0111848
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cofilin/tropomyosin family","termid":"PBO:0111848"}


id: PBO:0055712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LMBR1 domain containing 2","termid":"PBO:0055712"}


id: PBO:0091911
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meiotic Coiled-coil Protein","termid":"PBO:0091911"}


id: PBO:0003563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-endonuclease Apn2","termid":"PBO:0003563"}


id: PBO:0077044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid hormone receptor alpha","termid":"PBO:0077044"}


id: GO:0072421
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about damage to DNA is received and converted into a molecular signal, contributing to a DNA damage checkpoint.","definition_xrefs":["GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of DNA damage stimulus involved in DNA damage checkpoint (obsolete GO:0072421)","synonyms":[{"name":"DNA damage checkpoint sensor mechanism","type":"related"},{"name":"DNA damage checkpoint sensor process","type":"related"},{"name":"sensing involved in DNA damage checkpoint","type":"related"}],"termid":"GO:0072421"}


id: MONDO:0041755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"twin to twin transfusion syndrome","termid":"MONDO:0019805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"twin reversal arterial perfusion syndrome","secondary_identifiers":["UMLS:C1562817","MEDGEN:736778","SCTID:417006004"],"synonyms":[{"name":"twin reversal arterial perfusion syndrome","type":"exact"}],"termid":"MONDO:0041755","xrefs":{"Monarch":{"xref_id":"0041755"}}}


id: PBO:0113562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase complex gamma subunit, Ost3","termid":"PBO:0113562"}


id: PBO:0062851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OTOA pseudogene 1","termid":"PBO:0062851"}


id: MONDO:0001757
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the frontal sinus. Representative examples of benign neoplasms include Schneiderian papilloma and salivary gland-type adenoma. Representative examples of malignant neoplasms include carcinoma and lymphoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paranasal sinus neoplasm","termid":"MONDO:0005289"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frontal sinus neoplasm","secondary_identifiers":["UMLS:C0345672","SCTID:126678005","MEDGEN:91051","NCIT:C4419","DOID:1361","MONDO:0021214"],"synonyms":[{"name":"frontal sinus neoplasm (disease)","type":"exact"},{"name":"frontal sinus tumor","type":"exact"},{"name":"frontal sinus tumour","type":"exact"},{"name":"neoplasm of frontal sinus","type":"exact"},{"name":"neoplasm of the frontal sinus","type":"exact"},{"name":"tumor of frontal sinus","type":"exact"},{"name":"tumor of the frontal sinus","type":"exact"},{"name":"tumour of frontal sinus","type":"exact"},{"name":"tumour of the frontal sinus","type":"exact"}],"termid":"MONDO:0001757","xrefs":{"Monarch":{"xref_id":"0001757"}}}


id: PBO:0050083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group AT-hook 1 pseudogene 3","termid":"PBO:0050083"}


id: MONDO:0030293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary angioedema","termid":"MONDO:0019623"}],"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":"angioedema, hereditary, 5","secondary_identifiers":["MEDGEN:1780904","OMIM:619361","UMLS:C5543508"],"synonyms":[{"name":"HAE5","type":"exact"},{"name":"angioedema, hereditary, 5","type":"exact"}],"termid":"MONDO:0030293","xrefs":{"Monarch":{"xref_id":"0030293"}}}


id: PBO:0085704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in rRNA processing; required for maturation of the 35S primary transcript of pre-rRNA and for cleavage leading to mature 18S rRNA; homologous to eIF-4a, which is a DEAD box RNA-dependent ATPase with helicase activity","termid":"PBO:0085704"}


id: GO:1900806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of ergot alkaloid.","definition_xrefs":["GOC:TermGenie","GOC:di"],"gene_count":0,"genotype_count":0,"name":"obsolete ergot alkaloid catabolic process (obsolete GO:1900806)","synonyms":[{"name":"ergot alkaloid breakdown","type":"exact"},{"name":"ergot alkaloid catabolism","type":"exact"},{"name":"ergot alkaloid degradation","type":"exact"},{"name":"ergot alkaloids breakdown","type":"related"},{"name":"ergot alkaloids catabolic process","type":"related"},{"name":"ergot alkaloids catabolism","type":"related"},{"name":"ergot alkaloids degradation","type":"related"}],"termid":"GO:1900806"}


id: GO:0050691
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any host process that modulates the frequency, rate, or extent of the antiviral response of a host cell or organism.","definition_xrefs":["GOC:ai","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of defense response to virus","termid":"GO:0050688"}],"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 defense response to virus by host","synonyms":[{"name":"host regulation of antiviral response","type":"exact"},{"name":"regulation by host of antiviral response","type":"exact"},{"name":"regulation of antiviral response by host","type":"related"}],"termid":"GO:0050691"}


id: PBO:0052390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 27","termid":"PBO:0052390"}


id: PATO:0001277
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of orange hue and high saturation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orange","termid":"PATO:0000953"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"saturated orange","synonyms":[{"name":"bright orange","type":"related"}],"termid":"PATO:0001277"}


id: PBO:0028902
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_phosphorylation_during_cellular_response_to_DNA_damage","termid":"PBO:0028902"}


id: MONDO:0014153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cone-rod dystrophy in which the cause of the disease is a mutation in the RAB28 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy","termid":"MONDO:0015993"},{"relation_name":"is_a","term_name":"RAB28-related retinopathy","termid":"MONDO:0100448"}],"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":"cone-rod dystrophy 18","secondary_identifiers":["GARD:15953","UMLS:C3809299","MEDGEN:815629","OMIM:615374","DOID:0111024"],"synonyms":[{"name":"CORD18","type":"exact"},{"name":"RAB28 cone-rod dystrophy","type":"exact"},{"name":"cone-rod dystrophy 18","type":"exact"},{"name":"cone-rod dystrophy caused by mutation in RAB28","type":"exact"},{"name":"cone-rod dystrophy type 18","type":"exact"}],"termid":"MONDO:0014153","xrefs":{"Monarch":{"xref_id":"0014153"}}}


id: SO:0002114
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A protein coding transcript that contains a CDS but has one or more splice junctions >50bp downstream of stop codon, making it susceptible to nonsense mediated decay.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein_coding_primary_transcript","termid":"SO:0000120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMD_transcript","secondary_identifiers":["http://www.gencodegenes.org/gencode_biotypes.html"],"synonyms":[{"name":"NMD transcript","type":"exact"},{"name":"nonsense mediated decay transcript","type":"exact"},{"name":"protein_coding_NMD","type":"exact"}],"termid":"SO:0002114"}


id: PBO:0004990
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal disorders","termid":"PBO:0004990"}


id: PBO:0000725
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholestasis","termid":"PBO:0000725"}


id: MONDO:0000373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma in situ involving a gall bladder.","definition_xrefs":["MONDO:patterns/carcinoma_in_situ"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gallbladder carcinoma","termid":"MONDO:0003220"},{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"gall bladder carcinoma in situ","secondary_identifiers":["UMLS:C0345911","DOID:0050612","MEDGEN:87523","NCIT:C4439"],"synonyms":[{"name":"carcinoma in situ of gall bladder","type":"exact"},{"name":"gall bladder in situ carcinoma","type":"exact"},{"name":"stage 0 gall bladder carcinoma","type":"exact"}],"termid":"MONDO:0000373","xrefs":{"Monarch":{"xref_id":"0000373"}}}


id: GO:1990694
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the Golgi medial cisterna membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["PMID:24119662","GOC:bhm","PMID:16038056"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of Golgi medial cisterna membrane (obsolete GO:1990694)","synonyms":[{"name":"intrinsic component of medial-Golgi cisterna membrane","type":"exact"}],"termid":"GO:1990694"}


id: FYPO:0005586
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 phosphatidylethanolamine measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased phospholipid level","termid":"FYPO:0001288"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular phosphatidylethanolamine level","synonyms":[{"name":"increased cellular PE level","type":"exact"},{"name":"increased cellular phosphatidylethanolamine level during mitotic cell cycle","type":"related"},{"name":"increased cellular phosphatidylethanolamine level during vegetative growth","type":"exact"},{"name":"increased phosphatidylethanolamine accumulation","type":"related"}],"termid":"FYPO:0005586"}


id: MONDO:0001301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rumination disorder is the backward flow of recently eaten food from the stomach to the mouth. The food is then re-chewed and swallowed or spat out. A non-purposeful contraction of stomach muscles is involved in rumination. It may be initially triggered by a viral illness, emotional distress, or physical injury. In many cases, no underlying trigger is identified. Behavioral therapy is the mainstay of treatment.","direct_ancestors":[{"relation_name":"is_a","term_name":"eating disorder","termid":"MONDO:0005451"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rumination disorder","secondary_identifiers":["DOID:11507","SCTID:192014006","NCIT:C92567","MEDGEN:102311","icd11.foundation:879747857","MESH:D019959","ICD9:307.53","UMLS:C0154575"],"synonyms":[{"name":"psychogenic rumination","type":"exact"},{"name":"rumination","type":"exact"},{"name":"rumination syndrome","type":"related"}],"termid":"MONDO:0001301","xrefs":{"Monarch":{"xref_id":"0001301"}}}


id: PBO:0042659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule 8","termid":"PBO:0042659"}


id: PBO:0075369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRY-box transcription factor 7","termid":"PBO:0075369"}


id: SO:0001874
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A rearrangement breakpoint within the same chromosome.","definition_xrefs":["NCBI:th"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome_breakpoint","termid":"SO:0001021"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intrachromosomal_breakpoint","synonyms":[{"name":"intrachromosomal breakpoint","type":"exact"}],"termid":"SO:0001874"}


id: PR:Q9Y7Q2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gst1 gene.","definition_xrefs":["UniProtKB:Q9Y7Q2","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":"glutathione S-transferase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC191.09c","synonyms":[{"name":"GST-I (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gst1","type":"exact"}],"termid":"PR:Q9Y7Q2"}


id: GO:0051676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving pullulan, a neutral linear polysaccharide composed of repeating units of maltotriose joined by alpha-(1,6)-linkages.","definition_xrefs":["PMID:15013381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucan metabolic process","termid":"GO:0044042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"pullulan metabolic process","synonyms":[{"name":"pullulan metabolism","type":"exact"}],"termid":"GO:0051676"}


id: GO:0047956
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycerol + NADP+ = D-glyceraldehyde + NADPH.","definition_xrefs":["RHEA:23592"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"glycerol dehydrogenase (NADP+) activity","secondary_identifiers":["EC:1.1.1.72","MetaCyc:GLYCEROL-DEHYDROGENASE-NADP+-RXN"],"synonyms":[{"name":"glycerol dehydrogenase [NADP+] activity","type":"related"},{"name":"glycerol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0047956"}


id: PBO:0084580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Merged open reading frame; does not encode a discrete protein; YCL003W was originally annotated as an independent ORF, but as a result of a sequence change, it was merged with an adjacent ORF into a single reading frame, designated YCL004w","termid":"PBO:0084580"}


id: GO:0043059
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the speed, mechanical force, or rhythm of the anterior movement of an organism.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of locomotion","termid":"GO:0040012"},{"relation_name":"regulates","term_name":"forward locomotion","termid":"GO:0043056"}],"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 forward locomotion","termid":"GO:0043059"}


id: GO:0009790
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an embryo from its formation until the end of its embryonic life stage. The end of the embryonic stage is organism-specific. For example, for mammals, the process would begin with zygote formation and end with birth. For insects, the process would begin at zygote formation and end with larval hatching. For plant zygotic embryos, this would be from zygote formation to the end of seed dormancy. For plant vegetative embryos, this would be from the initial determination of the cell or group of cells to form an embryo until the point when the embryo becomes independent of the parent plant.","definition_xrefs":["GOC:isa_complete","GOC:mtg_sensu","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organism development","termid":"GO:0007275"}],"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":"embryo development","secondary_identifiers":["Wikipedia:Embryogenesis","GO:0009795","Reactome:R-HSA-5619507"],"synonyms":[{"name":"embryogenesis","type":"exact"},{"name":"embryogenesis and morphogenesis","type":"broad"},{"name":"embryonal development","type":"exact"}],"termid":"GO:0009790"}


id: GO:0090286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which cytoskeletal filaments are directly or indirectly linked to the nuclear membrane.","definition_xrefs":["GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete cytoskeletal anchoring at nuclear membrane (obsolete GO:0090286)","termid":"GO:0090286"}


id: PBO:0076129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUB1 regulator of transcription","termid":"PBO:0076129"}


id: PBO:0090406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GATOR2-SEACAT complex/COPII-coated vesicle component/nuclear pore outer ring WD repeat protein Sec13","termid":"PBO:0090406"}


id: GO:0044290
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The space bounded by the mitochondrial cristae membranes, continuous with the intermembrane space.","definition_xrefs":["NIF_Subcellular:sao508958414"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"mitochondrion","termid":"GO:0005739"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005739"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005739"],"is_obsolete":false,"name":"mitochondrial intracristal space","termid":"GO:0044290"}


id: GO:0043189
data:
  {"annotated_genes":["SJAG_00783","SJAG_02385","SJAG_00349","SJAG_04613","SJAG_03145","SJAG_01385","SJAG_02990","SJAG_03628","SJAG_04793","SJAG_04355","SJAG_00187","SJAG_03230","SJAG_03036","SJAG_03792","SJAG_03579","SJAG_04097","SJAG_05282"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[80856,75431,111031,74684,105967,80065,75557,69737,79204,78060,81807,94252,74731,81935,100873,106660,108831],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035267"}]},"cv_name":"cellular_component","definition":"A multisubunit complex that catalyzes the acetylation of histones H4 and H2A.","definition_xrefs":["GOC:rb","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"H4 histone acetyltransferase complex","termid":"GO:1902562"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00187":null,"SJAG_00349":null,"SJAG_00783":null,"SJAG_01385":null,"SJAG_02385":null,"SJAG_02990":null,"SJAG_03036":null,"SJAG_03145":null,"SJAG_03230":null,"SJAG_03579":null,"SJAG_03628":null,"SJAG_03792":null,"SJAG_04097":null,"SJAG_04355":null,"SJAG_04613":null,"SJAG_04793":null,"SJAG_05282":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"H4/H2A histone acetyltransferase complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"H4/H2A HAT complex","type":"exact"}],"termid":"GO:0043189","terms_by_termid":{"GO:0035267":null}}


id: GO:0002023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An eating behavior process whereby detection of a dietary excess results in a decrease in intake of nutrients.","definition_xrefs":["GOC:pg","PMID:12161655","GOC:pr","PMID:12840200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eating behavior","termid":"GO:0042755"},{"relation_name":"part_of","term_name":"response to dietary excess","termid":"GO:0002021"}],"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":"reduction of food intake in response to dietary excess","termid":"GO:0002023"}


id: MONDO:0030724
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"hearing loss, autosomal dominant 84","secondary_identifiers":["UMLS:C5676952","OMIM:619810","MEDGEN:1801352"],"synonyms":[{"name":"DFNA84","type":"exact"},{"name":"deafness, autosomal dominant 84","type":"narrow"}],"termid":"MONDO:0030724","xrefs":{"Monarch":{"xref_id":"0030724"}}}


id: MONDO:0005059
data:
  {"annotated_genes":["SJAG_03453","SJAG_05979","SJAG_03905","SJAG_01748","SJAG_01013","SJAG_01349"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89066,89064,89221,89065,89067,89222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"}]},"cv_name":"mondo","definition":"A malignant (clonal) hematologic disorder, involving hematopoietic stem cells and characterized by the presence of primitive or atypical myeloid or lymphoid cells in the bone marrow and the blood. Leukemias are classified as acute or chronic based on the degree of cellular differentiation and the predominant cell type present. Leukemia is usually associated with anemia, fever, hemorrhagic episodes, and splenomegaly. Common leukemias include acute myeloid leukemia, chronic myelogenous leukemia, acute lymphoblastic or precursor lymphoblastic leukemia, and chronic lymphocytic leukemia. Treatment is vital to patient survival; untreated, the natural course of acute leukemias is normally measured in weeks or months, while that of chronic leukemias is more often measured in months or years.","definition_xrefs":["NCIT:C3161"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lymphoid neoplasm","termid":"MONDO:0005157"},{"relation_name":"is_a","term_name":"hematopoietic and lymphoid cell neoplasm","termid":"MONDO:0044881"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01013":null,"SJAG_01349":null,"SJAG_01748":null,"SJAG_03453":null,"SJAG_03905":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"leukemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:208","ICD9:207.8","MESH:D007938","ICD9:208.90","SCTID:93143009","UMLS:C0023418","NANDO:2100002","ICD9:208.80","EFO:0000565","ICD9:207","DOID:1240","HP:0001909","ICD9:208.8","ICD9:207.80","ICD9:208.9","ICDO:9800/3","MEDGEN:9725"],"synonyms":[{"name":"blood (leukemia)","type":"exact"},{"name":"leukaemia (disease)","type":"exact"},{"name":"leukaemia NOS","type":"related"},{"name":"leukemia","type":"exact"},{"name":"leukemia (disease)","type":"exact"},{"name":"leukemia, disease","type":"exact"},{"name":"leukemia, malignant","type":"exact"},{"name":"leukemias","type":"exact"},{"name":"leukemias, general","type":"exact"}],"termid":"MONDO:0005059","terms_by_termid":{"MONDO:0018874":null},"xrefs":{"Monarch":{"xref_id":"0005059"}}}


id: FYPO:0008355
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of AMP 5'-nucleotidase activity is decreased.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal 5'-nucleotidase activity","termid":"FYPO:0008349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0000652","FYPO:0000654","FYPO:0001985"],"is_obsolete":false,"name":"decreased AMP 5'-nucleotidase activity","termid":"FYPO:0008355"}


id: PBO:0071756
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 P1 pseudogene 3","termid":"PBO:0071756"}


id: GO:0071478
data:
  {"annotated_genes":["SJAG_02860","SJAG_02818","SJAG_04190","SJAG_01262","SJAG_02334","SJAG_00729","SJAG_00272","SJAG_04150","SJAG_04877","SJAG_02828","SJAG_00814","SJAG_05197","SJAG_00863","SJAG_00208","SJAG_01010","SJAG_05242","SJAG_02200","SJAG_01648","SJAG_02199","SJAG_02182","SJAG_03898"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009785"},{"annotations":[121643,121642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071483"},{"annotations":[78653,111079,104761,97139],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[70512,114822,95543,89869,71793,97920,106164,60750,66022,67868,69013,99034,77439,107896,66914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070914"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an electromagnetic radiation stimulus. Electromagnetic radiation is a propagating wave in space with electric and magnetic components. These components oscillate at right angles to each other and to the direction of propagation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to radiation","termid":"GO:0009314"},{"relation_name":"is_a","term_name":"cellular response to abiotic stimulus","termid":"GO:0071214"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00208":null,"SJAG_00272":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00863":null,"SJAG_01010":null,"SJAG_01262":null,"SJAG_01648":null,"SJAG_02182":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02334":null,"SJAG_02818":null,"SJAG_02828":null,"SJAG_02860":null,"SJAG_03898":null,"SJAG_04150":null,"SJAG_04190":null,"SJAG_04877":null,"SJAG_05197":null,"SJAG_05242":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to radiation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:23873862":null},"synonyms":[{"name":"cellular response to electromagnetic radiation stimulus","type":"exact"},{"name":"cellular response to radiation stimulus","type":"exact"}],"termid":"GO:0071478","terms_by_termid":{"GO:0009785":null,"GO:0070914":null,"GO:0071483":null,"GO:1904161":null}}


id: MONDO:0859375
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":"developmental delay with hypotonia, myopathy, and brain abnormalities","secondary_identifiers":["OMIM:620240","MEDGEN:1840906","UMLS:C5830270"],"termid":"MONDO:0859375","xrefs":{"Monarch":{"xref_id":"0859375"}}}


id: MONDO:1012580
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leukocyte adhesion deficiency that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"},{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukocyte adhesion deficiency, non-human animal","termid":"MONDO:1012580","xrefs":{"Monarch":{"xref_id":"1012580"}}}


id: PBO:0002079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S5 (predicted)","termid":"PBO:0002079"}


id: GO:1990486
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a fatty acid in the absence of oxygen. A fatty acid is any of the aliphatic monocarboxylic acids that can be liberated by hydrolysis from naturally occurring fats and oils. Fatty acids are predominantly straight-chain acids of 4 to 24 carbon atoms, which may be saturated or unsaturated; branched fatty acids and hydroxy fatty acids also occur, and very long chain acids of over 30 carbons are found in waxes.","definition_xrefs":["GOC:mengo_curators","PMID:17329794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid catabolic process","termid":"GO:0009062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"anaerobic fatty acid catabolic process","synonyms":[{"name":"anaerobic fatty acid degradation","type":"exact"}],"termid":"GO:1990486"}


id: GO:0052712
data:
  {"annotated_genes":["SJAG_01219"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052714"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: inositol phosphosphingolipid + H2O = sphingolipid + phosphorylinositol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase C activity","termid":"GO:0004629"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01219":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"inositol phosphosphingolipid phospholipase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0052712","terms_by_termid":{"GO:0052714":null}}


id: GO:0047090
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: benzoyl-CoA + H+ + NADPH + O2 = 3-hydroxybenzoyl-CoA + H2O + NADP+.","definition_xrefs":["EC:1.14.13.58","RHEA:23216"],"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":"benzoyl-CoA 3-monooxygenase activity","secondary_identifiers":["KEGG_REACTION:R02449","MetaCyc:1.14.13.58-RXN"],"synonyms":[{"name":"benzoyl-CoA 3-hydroxylase activity","type":"exact"},{"name":"benzoyl-CoA,NADPH:oxygen oxidoreductase (3-hydroxylating)","type":"related"}],"termid":"GO:0047090"}


id: GO:0004419
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-hydroxy-3-methylglutaryl-CoA = acetoacetate + acetyl-CoA.","definition_xrefs":["EC:4.1.3.4","RHEA:24404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxo-acid-lyase activity","termid":"GO:0016833"}],"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:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"hydroxymethylglutaryl-CoA lyase activity","secondary_identifiers":["Reactome:R-HSA-74180","MetaCyc:HYDROXYMETHYLGLUTARYL-COA-LYASE-RXN","Reactome:R-HSA-6788597","KEGG_REACTION:R01360"],"synonyms":[{"name":"(S)-3-hydroxy-3-methylglutaryl-CoA acetoacetate-lyase (acetyl-CoA-forming)","type":"related"},{"name":"(S)-3-hydroxy-3-methylglutaryl-CoA acetoacetate-lyase activity","type":"related"},{"name":"3-hydroxy-3-methylglutarate-CoA lyase activity","type":"related"},{"name":"3-hydroxy-3-methylglutaryl CoA cleaving enzyme","type":"related"},{"name":"3-hydroxy-3-methylglutaryl coenzyme A lyase activity","type":"related"},{"name":"3-hydroxy-3-methylglutaryl-CoA lyase activity","type":"related"},{"name":"HMG-CoA lyase activity","type":"related"},{"name":"hydroxymethylglutaryl coenzyme A lyase activity","type":"related"},{"name":"hydroxymethylglutaryl coenzyme A-cleaving enzyme","type":"related"}],"termid":"GO:0004419"}


id: PBO:0113201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Methionine-R-sulfoxide reductase; reduces the R enantiomer of free Met-SO, in contrast to Ycl033Cp which reduces Met-R-SO in a peptide linkage; has a role in protection against oxidative stress; capable of binding and degrading patulin, a polyketide mycotoxin, forming E-ascladiol; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0113201"}


id: GO:0044608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a C-terminal peptidyl-threonine to form peptidyl-L-threonine methyl ester.","definition_xrefs":["RESID:AA0507"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-L-threonine methyl ester biosynthetic process from peptidyl-threonine (obsolete GO:0044608)","synonyms":[{"name":"peptidyl-threonine esterification","type":"exact"}],"termid":"GO:0044608"}


id: PBO:0069589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 863, pseudogene","termid":"PBO:0069589"}


id: PBO:0054881
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 2295","termid":"PBO:0054881"}


id: PBO:0062449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 116 pseudogene","termid":"PBO:0062449"}


id: PBO:0065992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAI1 antisense RNA 1","termid":"PBO:0065992"}


id: PBO:0061993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily D member 2","termid":"PBO:0061993"}


id: FYPO:0004738
data:
  {"alleles_by_uniquename":{"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_04280:allele-1":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-1"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[121535],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"}],"single_locus_phenotype":[{"annotations":[121359,121593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002998"},{"annotations":[121456],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0002026"},{"annotations":[121424,121671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[121536],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which actin contractile ring organization is abnormal. The process normally results in the assembly, arrangement of constituent parts, or disassembly of the actomyosin contractile ring.","definition_xrefs":["PomBase:mah","GO:0044837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cytoskeleton organization during vegetative growth","termid":"FYPO:0000801"},{"relation_name":"is_a","term_name":"abnormal cellular component assembly during vegetative growth","termid":"FYPO:0001354"},{"relation_name":"is_a","term_name":"abnormal cell cycle process","termid":"FYPO:0002734"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01143":null,"SJAG_02392":null,"SJAG_02592":null,"SJAG_04280":null,"SJAG_04522":null},"genotype_count":6,"genotypes_by_uniquename":{"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-1","expression":"Not assayed or wild type"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000631","FYPO:0005447","FYPO:0004803","FYPO:0001320"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_02392","SJAG_04522","SJAG_01143","SJAG_04280"],"name":"abnormal actomyosin contractile ring organization","references_by_uniquename":{"PMID:25866389":null,"PMID:27059155":null,"PMID:30664646":null,"PMID:32915139":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_04522","SJAG_02392","SJAG_01143","SJAG_02592"],"single_locus_genotype_uniquenames":["rga4delta","pom1delta","mid1delta","sty1delta"],"synonyms":[{"name":"abnormal actomyosin contractile ring organisation","type":"exact"},{"name":"abnormal actomyosin contractile ring organization during mitotic cell cycle","type":"related"},{"name":"abnormal actomyosin contractile ring organization during vegetative growth","type":"exact"},{"name":"abnormal contractile ring organization","type":"exact"},{"name":"abnormal mitotic contractile ring organization","type":"exact"}],"termid":"FYPO:0004738","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000248":null,"FYECO:0000338":null,"FYPO:0000729":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO:0002998":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:0010964
data:
  {"annotated_genes":["SJAG_03664","SJAG_04369"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119766],"is_not":false,"summary":null,"term":"GO:0010964"},{"annotations":[110455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060906"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of small non-coding RNA-mediated heterochromatin formation.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heterochromatin formation","termid":"GO:0031445"},{"relation_name":"is_a","term_name":"regulation of gene silencing by regulatory ncRNA","termid":"GO:0060966"},{"relation_name":"regulates","term_name":"regulatory ncRNA-mediated heterochromatin formation","termid":"GO:0031048"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03664":null,"SJAG_04369":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0010467","GO:0006325","GO:0008150"],"is_obsolete":false,"name":"regulation of regulatory ncRNA-mediated heterochromatin formation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of RNAi-mediated heterochromatin assembly","type":"exact"},{"name":"regulation of chromatin silencing by small RNA","type":"narrow"},{"name":"regulation of heterochromatin assembly by small RNA","type":"narrow"},{"name":"regulation of ncRNA-mediated heterochromatin formation","type":"exact"},{"name":"regulation of small non-coding RNA-mediated heterochromatin formation","type":"narrow"}],"termid":"GO:0010964","terms_by_termid":{"GO:0010964":null,"GO:0060906":null}}


id: PBO:0088624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH domain RNA-binding protein","termid":"PBO:0088624"}


id: MONDO:0001781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign mesothelial tumor of the serosal surface of the uterine body and myometrium. It is characterized by the presence of gland-like structures.","definition_xrefs":["NCIT:C27250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign mesothelioma","termid":"MONDO:0002373"},{"relation_name":"is_a","term_name":"adenomatoid tumor","termid":"MONDO:0004230"},{"relation_name":"is_a","term_name":"benign neoplasm of corpus uteri","termid":"MONDO:0021525"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterine corpus adenomatoid tumor","secondary_identifiers":["MEDGEN:234464","UMLS:C1336902","DOID:1371"],"synonyms":[{"name":"body of uterus adenomatoid tumor","type":"exact"},{"name":"body of uterus adenomatoid tumour","type":"exact"},{"name":"uterine corpus adenomatoid tumor","type":"exact"},{"name":"uterine corpus localised epithelial mesothelioma","type":"exact"},{"name":"uterine corpus localized epithelial mesothelioma","type":"exact"}],"termid":"MONDO:0001781","xrefs":{"Monarch":{"xref_id":"0001781"}}}


id: MONDO:0013277
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SPTAN1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"infantile spasms","termid":"MONDO:0018097"},{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 5","secondary_identifiers":["MEDGEN:462081","OMIM:613477","DOID:0080438","UMLS:C3150731","GARD:12949"],"synonyms":[{"name":"DEE5","type":"exact"},{"name":"EIEE5","type":"exact"},{"name":"SPTAN1 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 5","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in SPTAN1","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 5","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 5","type":"exact"}],"termid":"MONDO:0013277","xrefs":{"Monarch":{"xref_id":"0013277"}}}


id: MONDO:0043156
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nephrotic syndrome","termid":"MONDO:0005377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"nephrotic syndrome ocular anomalies","secondary_identifiers":["MESH:C536403","MEDGEN:419736","UMLS:C2931188"],"synonyms":[{"name":"Glastre Cochat Bouvier syndrome","type":"related"},{"name":"familial infantile nephrotic syndrome with ocular abnormalities","type":"related"}],"termid":"MONDO:0043156","xrefs":{"Monarch":{"xref_id":"0043156"}}}


id: PBO:0087631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the DSC ubiquitin ligase complex; protein of unknown function that localizes to the ER and vacuole lumen; overexpression affects endocytic protein trafficking; ortholog of fission yeast dsc3","termid":"PBO:0087631"}


id: MONDO:0005848
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"I would say the hematogenous widespread dissemination of tuberculosis in the body. The term derives from the chest X-ray image of the tiny (1-5 mm) tuberculosis lesions which are seen through out the lung parenchyma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrapulmonary tuberculosis","termid":"MONDO:0000368"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"miliary tuberculosis","secondary_identifiers":["DOID:9861","UMLS:C0041321","ICD9:018","ICD10CM:A19","EFO:0007368","icd11.foundation:861638547","ICD9:018.9","MEDGEN:21726","MESH:D014391","ICD9:018.80","ICD9:018.90","NCIT:C35086","SCTID:47604008"],"synonyms":[{"name":"acute miliary tuberculosis","type":"exact"},{"name":"disseminated tuberculosis","type":"exact"},{"name":"generalised tuberculosis","type":"exact"},{"name":"generalized tuberculosis","type":"exact"},{"name":"tuberculosis miliaris disseminata","type":"exact"}],"termid":"MONDO:0005848","xrefs":{"Monarch":{"xref_id":"0005848"}}}


id: PBO:0040747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain cytoplasmic RNA 1, pseudogene 2","termid":"PBO:0040747"}


id: PBO:0082938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic class E vacuolar protein sorting (VPS) factor; coordinates protein sorting and deubiquitination in the multivesicular body (MVB) pathway by recruiting Doa4p to endosomes","termid":"PBO:0082938"}


id: GO:1990914
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the plasma membrane consisting of the gene products that penetrate only the periplasmic side of the membrane.","definition_xrefs":["GOC:bhm","PMID:15919996"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of periplasmic side of plasma membrane (obsolete GO:1990914)","termid":"GO:1990914"}


id: GO:0043533
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to inositol 1,3,4,5 tetrakisphosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"alcohol binding","termid":"GO:0043178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"inositol 1,3,4,5 tetrakisphosphate binding","synonyms":[{"name":"IP4 binding","type":"exact"},{"name":"InsP4 binding","type":"exact"}],"termid":"GO:0043533"}


id: MONDO:0001274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"anus disorder","termid":"MONDO:0002519"}],"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":"anal spasm","secondary_identifiers":["ICD10CM:K59.4","SCTID:17440005","DOID:11374","icd11.foundation:647005938","MEDGEN:508910","UMLS:C0152167","ICD9:564.6"],"termid":"MONDO:0001274","xrefs":{"Monarch":{"xref_id":"0001274"}}}


id: PR:000050513
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A meiotic recombination protein rec8 (Schizosaccharomyces pombe) that has been phosphorylated at the position equivalent to Ser-412 of the amino acid sequence represented by UniProtKB:P36626. Example: UniProtKB:P36626, Ser-412, MOD:00046.","definition_xrefs":["PMID:33888556","PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic recombination protein rec8 (Schizosaccharomyces pombe)","termid":"PR:000050510"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rec8/Phos(S412)","pombase_gene_id":"SPBC29A10.14","synonyms":[{"name":"PomBase_original_PRO_term_name: meiotic recombination protein rec8 phosphorylated 3 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-rec8/Phos:3","type":"exact"},{"name":"UniProtKB:P36626, Ser-412, MOD:00046","type":"narrow"},{"name":"rec8/Phos(S412)","type":"exact"}],"termid":"PR:000050513"}


id: GO:0000102
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of L-methionine from one side of a membrane to the other, up its concentration gradient. The transporter binds the solute and undergoes a series of conformational changes. Transport works equally well in either direction and is driven by a chemiosmotic source of energy. Secondary active transporters include symporters and antiporters.","definition_xrefs":["GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neutral L-amino acid secondary active transmembrane transporter activity","termid":"GO:0005294"},{"relation_name":"is_a","term_name":"L-methionine transmembrane transporter activity","termid":"GO:0015191"}],"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:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"L-methionine secondary active transmembrane transporter activity","synonyms":[{"name":"L-methionine porter activity","type":"related"}],"termid":"GO:0000102"}


id: GO:0070230
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of lymphocyte death by apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis","GOC:add","ISBN:0781765196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lymphocyte apoptotic process","termid":"GO:0070228"},{"relation_name":"is_a","term_name":"positive regulation of leukocyte apoptotic process","termid":"GO:2000108"},{"relation_name":"positively_regulates","term_name":"lymphocyte apoptotic process","termid":"GO:0070227"}],"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 lymphocyte apoptotic process","synonyms":[{"name":"activation of lymphocyte apoptosis","type":"narrow"},{"name":"positive regulation of lymphocyte apoptosis","type":"narrow"},{"name":"stimulation of lymphocyte apoptosis","type":"narrow"},{"name":"up regulation of lymphocyte apoptosis","type":"exact"},{"name":"up-regulation of lymphocyte apoptosis","type":"exact"},{"name":"upregulation of lymphocyte apoptosis","type":"exact"}],"termid":"GO:0070230"}


id: RO:0002616
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"related_via_evidence_or_inference_to","termid":"RO:0002616"}


id: MOD:00459
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(13)C labeled succinyl group.","definition_xrefs":["Unimod:66#N-term","PubMed:12175151","PubMed:11857757"],"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(13)C labeled alpha-amino succinylated residue","synonyms":[{"name":"Succinic anhydride labeling reagent, heavy form (+4amu, 4C13), N-term & K","type":"related"},{"name":"Succinyl:13C(4)","type":"related"}],"termid":"MOD:00459"}


id: MONDO:0031698
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic intestinal disease due to fat malabsorption (obsolete MONDO:0031698)","secondary_identifiers":["Orphanet:363306"],"termid":"MONDO:0031698","xrefs":{"Monarch":{"xref_id":"0031698"}}}


id: MONDO:0000019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ectodermal dysplasia (obsolete MONDO:0000019)","termid":"MONDO:0000019","xrefs":{"Monarch":{"xref_id":"0000019"}}}


id: PBO:0002265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH-dependent flavin oxidoreductase (predicted)","termid":"PBO:0002265"}


id: PBO:0077305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 44","termid":"PBO:0077305"}


id: PBO:0076333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin 2","termid":"PBO:0076333"}


id: SO:0000892
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is positively autoregulated.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"positively_autoregulated","termid":"SO:0000475"},{"relation_name":"is_a","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"positively_autoregulated_gene","synonyms":[{"name":"positively autoregulated gene","type":"exact"}],"termid":"SO:0000892"}


id: GO:0047870
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N(6)-dimethylallyladenine + S-adenosyl-L-methionine(1+) = S-methyl-5'-thioadenosine + discadenine + H+.","definition_xrefs":["RHEA:19581","EC:2.5.1.24"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016765"}],"interesting_parent_ids":["GO:0016765","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"discadenine synthase activity","secondary_identifiers":["KEGG_REACTION:R03726","MetaCyc:DISCADENINE-SYNTHASE-RXN"],"synonyms":[{"name":"S-adenosyl-L-methionine:6-N-(Delta2-isopentenyl)-adenine 3-(3-amino-3-carboxypropyl)-transferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:N6-(Delta2-isopentenyl)-adenine 3-(3-amino-3-carboxypropyl)-transferas","type":"related"},{"name":"discadenine synthetase activity","type":"related"}],"termid":"GO:0047870"}


id: PBO:0067307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 393, pseudogene","termid":"PBO:0067307"}


id: PBO:0061763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ornithine aminotransferase","termid":"PBO:0061763"}


id: PBO:0066013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA guanine-7 methyltransferase activating subunit like","termid":"PBO:0066013"}


id: GO:0047513
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + methyl-2-alpha-L-fucopyranosyl-beta-D-galactoside = L-fucose + methyl beta-D-galactoside.","definition_xrefs":["EC:3.2.1.63","MetaCyc:12-ALPHA-L-FUCOSIDASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-L-fucosidase activity","termid":"GO:0004560"}],"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:0016798"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016798","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"1,2-alpha-L-fucosidase activity","secondary_identifiers":["RHEA:10816"],"synonyms":[{"name":"2-alpha-L-fucopyranosyl-beta-D-galactoside fucohydrolase activity","type":"related"},{"name":"almond emulsin fucosidase II activity","type":"narrow"},{"name":"almond emulsin fucosidase activity","type":"related"},{"name":"alpha-(1->2)-L-fucosidase activity","type":"related"}],"termid":"GO:0047513"}


id: GO:0009820
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving alkaloids, nitrogen containing natural products which are not otherwise classified as peptides, nonprotein amino acids, amines, cyanogenic glycosides, glucosinolates, cofactors, phytohormones or primary metabolites (such as purine or pyrimidine bases).","definition_xrefs":["GOC:lr","ISBN:0122146743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"alkaloid metabolic process","synonyms":[{"name":"alkaloid metabolism","type":"exact"}],"termid":"GO:0009820"}


id: GO:0055008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of cardiac muscle tissue are generated and organized.","definition_xrefs":["GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle tissue morphogenesis","termid":"GO:0060415"},{"relation_name":"part_of","term_name":"heart morphogenesis","termid":"GO:0003007"},{"relation_name":"part_of","term_name":"cardiac muscle tissue development","termid":"GO:0048738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cardiac muscle tissue morphogenesis","synonyms":[{"name":"heart muscle morphogenesis","type":"exact"},{"name":"myocardium morphogenesis","type":"broad"}],"termid":"GO:0055008"}


id: MONDO:0054637
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome-like disorder with loose anagen hair","termid":"MONDO:0011899"}],"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":"Noonan syndrome-like disorder with loose anagen hair 1","secondary_identifiers":["UMLS:C4478716","MEDGEN:1379805","NCIT:C176939","OMIM:607721","DOID:0080692"],"synonyms":[{"name":"NSLH","type":"broad"},{"name":"NSLH1","type":"exact"},{"name":"Noonan syndrome-like disorder with loose anagen hair 1","type":"exact"},{"name":"Noonan syndrome-like with loose anagen hair 1","type":"exact"},{"name":"Tosti syndrome","type":"related"}],"termid":"MONDO:0054637","xrefs":{"Monarch":{"xref_id":"0054637"}}}


id: MONDO:0019091
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring.","definition_xrefs":["Orphanet:70589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bronchopulmonary dysplasia","secondary_identifiers":["SCTID:67569000","GARD:5962","NCIT:C90599","icd11.foundation:1462855296","MEDGEN:2738","NORD:874","MESH:D001997","MedDRA:10006475","DOID:11650","UMLS:C0006287"],"synonyms":[{"name":"BPD","type":"exact"}],"termid":"MONDO:0019091","xrefs":{"Monarch":{"xref_id":"0019091"}}}


id: GO:0070634
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of ammonium ions from one side of an epithelium to the other.","definition_xrefs":["GOC:mah","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transepithelial transport","termid":"GO:0070633"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"transepithelial ammonium transport","termid":"GO:0070634"}


id: GO:0015493
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: lysine(out) + H+(out) = lysine(in) + H+(in).","definition_xrefs":["TC:2.A.3.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid:proton symporter activity","termid":"GO:0005280"},{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"lysine:proton symporter activity","synonyms":[{"name":"lysine:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015493"}


id: GO:0050093
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: methanol + NAD+ = formaldehyde + H+ + NADH.","definition_xrefs":["EC:1.1.1.244","RHEA:19401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol dehydrogenase (NAD+) activity","termid":"GO:0004022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"methanol dehydrogenase (NAD+) activity","secondary_identifiers":["MetaCyc:METHANOL-DEHYDROGENASE-RXN","KEGG_REACTION:R00605"],"synonyms":[{"name":"methanol dehydrogenase activity","type":"broad"},{"name":"methanol:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0050093"}


id: FYPO:0007220
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 acetylation of lysine at position 9 of histone H3 in regions containing protein-coding genes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:31260531"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H3-K9 acetylation during vegetative growth","termid":"FYPO:0003223"}],"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"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal histone H3-K9 acetylation at protein coding gene during vegetative growth","synonyms":[{"name":"normal histone H3-K9 acetylation at protein coding gene during mitotic cell cycle","type":"related"},{"name":"normal histone H3-K9 acetylation at protein-coding gene during vegetative growth","type":"exact"},{"name":"normal histone H3K9 acetylation at protein coding gene during vegetative growth","type":"exact"}],"termid":"FYPO:0007220"}


id: PBO:0046826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid binding protein 4","termid":"PBO:0046826"}


id: GO:0070840
data:
  {"annotated_genes":["SJAG_02651","SJAG_00594"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106489,106823],"is_not":false,"summary":null,"term":"GO:0070840"}]},"cv_name":"molecular_function","definition":"Binding to a dynein complex, a protein complex that contains two or three dynein heavy chains and several light chains, and has microtubule motor activity.","definition_xrefs":["GOC:mah","GOC:BHF","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00594":null,"SJAG_02651":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"dynein complex binding","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0045502"],"synonyms":[{"name":"dynein binding","type":"related"}],"termid":"GO:0070840","terms_by_termid":{"GO:0070840":null}}


id: PR:000037033
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitotic cohesin complex subunit Psm3/Smc3 (Schizosaccharomyces pombe) that has been acetylated on two Lys residues equivalent to Lys-105 and Lys-106 of the amino acid sequence represented by UniProtKB:O42649. Example: UniProtKB:O42649, Lys-105/Lys-106, MOD:00723.","definition_xrefs":["PRO:DAN","PMID:26687354","PomBase:VW"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic cohesin complex subunit Psm3/Smc3 (Schizosaccharomyces pombe)","termid":"PR:000037032"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psm3/Ac(K105,K106)","pombase_gene_id":"SPAC10F6.09c","synonyms":[{"name":"PomBase_original_PRO_term_name: mitotic cohesin complex subunit Psm3/Smc3 acetylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-psm3/Ac:1","type":"exact"},{"name":"UniProtKB:O42649, Lys-105/Lys-106, MOD:00723","type":"narrow"},{"name":"cohesin complex Psm3 subunit acetylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"psm3/Ac(K105,K106)","type":"exact"},{"name":"structural maintenance of chromosomes protein 3 acetylated 1 (Schizosaccharomyces pombe)","type":"exact"}],"termid":"PR:000037033"}


id: GO:0044130
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont stops, prevents or reduces its increase in size or mass within the cells or tissues of the host organism. The host is defined as the larger of the organisms involved in the symbiotic interaction.","definition_xrefs":["GOC:jl","GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of growth of symbiont in host (obsolete GO:0044130)","termid":"GO:0044130"}


id: MONDO:0000500
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that arises from the tongue. It usually presents as a painful ulcerated or nodular lesion. The size of the tumor and the status of the lymph nodes are the most important factors that determine prognosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tongue cancer","termid":"MONDO:0004631"},{"relation_name":"is_a","term_name":"oral cavity squamous cell carcinoma","termid":"MONDO:0004958"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"tongue squamous cell carcinoma","secondary_identifiers":["DOID:0050865","MEDGEN:91153","SCTID:276952000","UMLS:C0349566","NCIT:C4648"],"synonyms":[{"name":"scc of the tongue","type":"exact"},{"name":"scc of tongue","type":"exact"},{"name":"squamous cell carcinoma of the tongue","type":"exact"},{"name":"squamous cell carcinoma of tongue","type":"exact"},{"name":"tongue scc","type":"exact"},{"name":"tongue squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0000500","xrefs":{"Monarch":{"xref_id":"0000500"}}}


id: PBO:0012023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongator subunit Elp1 (predicted)","termid":"PBO:0012023"}


id: GO:0045040
data:
  {"annotated_genes":["SJAG_02034","SJAG_01951","SJAG_03502","SJAG_02355","SJAG_02361","SJAG_02797","SJAG_01780","SJAG_00569","SJAG_03416"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59047,71702,78377,100144,100495,109526,112023,112376,113778],"is_not":false,"summary":null,"term":"GO:0045040"}]},"cv_name":"biological_process","definition":"The process comprising the insertion of proteins from outside the organelle into the mitochondrial outer membrane, mediated by large outer membrane translocase complexes.","definition_xrefs":["GOC:mcc","GOC:vw","PMID:18672008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial transport","termid":"GO:0006839"},{"relation_name":"is_a","term_name":"intracellular protein transport","termid":"GO:0006886"},{"relation_name":"is_a","term_name":"outer mitochondrial membrane organization","termid":"GO:0007008"},{"relation_name":"is_a","term_name":"establishment of protein localization to mitochondrial membrane","termid":"GO:0090151"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00569":null,"SJAG_01780":null,"SJAG_01951":null,"SJAG_02034":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_02797":null,"SJAG_03416":null,"SJAG_03502":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007005","GO:0051179","GO:0006810","GO:0008150","GO:0061024"],"is_obsolete":false,"name":"protein insertion into mitochondrial outer membrane","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial outer membrane protein import","type":"exact"},{"name":"protein import into mitochondrial outer membrane","type":"exact"},{"name":"protein transport into mitochondrial outer membrane","type":"exact"}],"termid":"GO:0045040","terms_by_termid":{"GO:0045040":null}}


id: PBO:0040319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase F1 subunit gamma pseudogene 1","termid":"PBO:0040319"}


id: GO:0046570
data:
  {"annotated_genes":["SJAG_02689","SJAG_02293"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[80139,82086],"is_not":false,"summary":null,"term":"GO:0046570"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-methyl-5-thio-D-ribulose 1-phosphate = 5-(methylthio)-2,3-dioxopentyl phosphate + H2O.","definition_xrefs":["EC:4.2.1.109","RHEA:15549"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02293":null,"SJAG_02689":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"methylthioribulose 1-phosphate dehydratase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-1237140","KEGG_REACTION:R07392","GO:0043809","MetaCyc:R145-RXN"],"synonyms":[{"name":"1-PMT-ribulose dehydratase activity","type":"related"},{"name":"5-methylthioribulose-1-phosphate 4-dehydratase activity","type":"exact"},{"name":"S-methyl-5-thio-D-ribulose-1-phosphate hydro-lyase [5-(methylthio)-2,3-dioxopentyl-phosphate-forming]","type":"related"},{"name":"S-methyl-5-thio-D-ribulose-1-phosphate hydro-lyase activity","type":"exact"},{"name":"S-methyl-5-thio-D-ribulose-1-phosphate hydro-lyase[5-(methylthio)-2,3-dioxopentyl-phosphate-forming]","type":"exact"},{"name":"methylthioribulose-1-phosphate dehydratase activity","type":"exact"}],"termid":"GO:0046570","terms_by_termid":{"GO:0046570":null}}


id: GO:0060954
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a neural crest-derived cardiac glial cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac glial cell development","termid":"GO:0060952"},{"relation_name":"part_of","term_name":"neural crest-derived cardiac glial cell differentiation","termid":"GO:0060951"}],"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":"neural crest-derived cardiac glial cell development","termid":"GO:0060954"}


id: GO:0098799
data:
  {"annotated_genes":["SJAG_00569","SJAG_03515","SJAG_03358","SJAG_05259","SJAG_03502","SJAG_02361","SJAG_00948","SJAG_04996","SJAG_03416","SJAG_01780","SJAG_03710","SJAG_01134","SJAG_01305","SJAG_03345","SJAG_01929","SJAG_04370","SJAG_01951","SJAG_02355","SJAG_03415"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[106759,117771,91120],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036266"},{"annotations":[118619,71741,81857,76534,71698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032865"},{"annotations":[112384,113776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140595"},{"annotations":[92241,62573,75139,71697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001401"},{"annotations":[108127,101456,92766,109523,109547,101341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140596"}]},"cv_name":"cellular_component","definition":"Any protein complex that is part of the outer mitochondrial membrane.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"mitochondrial protein-containing complex","termid":"GO:0098798"},{"relation_name":"part_of","term_name":"mitochondrial outer membrane","termid":"GO:0005741"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00569":null,"SJAG_00948":null,"SJAG_01134":null,"SJAG_01305":null,"SJAG_01780":null,"SJAG_01929":null,"SJAG_01951":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_03345":null,"SJAG_03358":null,"SJAG_03415":null,"SJAG_03416":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03710":null,"SJAG_04370":null,"SJAG_04996":null,"SJAG_05259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005739"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005739","GO:0032991"],"is_obsolete":false,"name":"outer mitochondrial membrane protein complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0098799","terms_by_termid":{"GO:0001401":null,"GO:0032865":null,"GO:0036266":null,"GO:0140595":null,"GO:0140596":null}}


id: PBO:0090077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoplasmic aspartate aminotransferase Caa1","termid":"PBO:0090077"}


id: PBO:0078203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 6-5","termid":"PBO:0078203"}


id: PBO:0003448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidyl-N-methylethanolamine N-methyltransferase (predicted)","termid":"PBO:0003448"}


id: PBO:0075922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST13, Hsp70 interacting protein pseudogene 14","termid":"PBO:0075922"}


id: MONDO:0024488
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A modifier that can be applied to a tumor class describing abnormal tumor histology or morphology. It is an indicator of how quickly a tumor is likely to grow and spread","direct_ancestors":[{"relation_name":"is_a","term_name":"disease characteristic","termid":"MONDO:0021125"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor grading characteristic","termid":"MONDO:0024488","xrefs":{"Monarch":{"xref_id":"0024488"}}}


id: PBO:0001119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-phosphatidylinositol 4-kinase Lsb6 (predicted)","termid":"PBO:0001119"}


id: GO:0018940
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving orcinol (5-methyl-1,3-benzenediol), an aromatic compound derived from the fermentation of lichen, and synthesized, probably as a fungicide, by some higher plants.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"},{"relation_name":"is_a","term_name":"toluene-containing compound metabolic process","termid":"GO:0072490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"orcinol metabolic process","secondary_identifiers":["MetaCyc:P342-PWY","UM-BBD_pathwayID:orc"],"synonyms":[{"name":"orcin metabolic process","type":"exact"},{"name":"orcin metabolism","type":"exact"},{"name":"orcinol metabolism","type":"exact"}],"termid":"GO:0018940"}


id: MONDO:0004491
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant tumor arising from trophoblastic cells in the uterus during pregnancy. Approximately half of the cases develop from a complete hydatidiform mole. There is often marked elevation of human chorionic gonadotropin (hCG) in the blood. Choriocarcinomas disseminate rapidly through the hematogenous route; the lungs are most frequently affected.","definition_xrefs":["NCIT:C27246"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant germ cell tumor of corpus uteri","termid":"MONDO:0016273"},{"relation_name":"is_a","term_name":"gestational choriocarcinoma","termid":"MONDO:0020550"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"uterine corpus choriocarcinoma","secondary_identifiers":["MEDGEN:234466","DOID:8187","DOID:8188","UMLS:C1336904","ONCOTREE:UCCA"],"synonyms":[{"name":"body of uterus choriocarcinoma (disease)","type":"exact"},{"name":"body of uterus gestational choriocarcinoma","type":"exact"},{"name":"choriocarcinoma","type":"related"},{"name":"gestational choriocarcinoma of body of uterus","type":"exact"},{"name":"gestational uterine corpus choriocarcinoma","type":"exact"},{"name":"uterine corpus gestational choriocarcinoma","type":"exact"}],"termid":"MONDO:0004491","xrefs":{"Monarch":{"xref_id":"0004491"}}}


id: FYPO:0000024
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which the cell diameter is larger than normal and the cell length is shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"increased cell diameter","termid":"FYPO:0006615"},{"relation_name":"is_a","term_name":"abnormal vegetative cell shape","termid":"FYPO:0002196"},{"relation_name":"is_a","term_name":"increased cell diameter","termid":"FYPO:0006615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"stubby vegetative cell","synonyms":[{"name":"cell morphology, stubby cells","type":"exact"},{"name":"stubby cell during mitotic cell cycle","type":"related"},{"name":"stubby cell during vegetative growth","type":"exact"},{"name":"watermelon-shaped vegetative cell","type":"exact"}],"termid":"FYPO:0000024"}


id: MONDO:0014697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any common variable immunodeficiency in which the cause of the disease is a mutation in the NFKB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"common variable immunodeficiency","termid":"MONDO:0015517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"immunodeficiency, common variable, 12","secondary_identifiers":["OMIM:616576","DOID:0081154","GARD:16141","MEDGEN:906018","UMLS:C4225277"],"synonyms":[{"name":"CVID12","type":"related"},{"name":"NFKB1 common variable immunodeficiency","type":"exact"},{"name":"NFKB1 deficiency","type":"related"},{"name":"common variable immunodeficiency caused by mutation in NFKB1","type":"exact"},{"name":"immunodeficiency, common variable, 12","type":"exact"},{"name":"immunodeficiency, common variable, type 12","type":"exact"}],"termid":"MONDO:0014697","xrefs":{"Monarch":{"xref_id":"0014697"}}}


id: GO:0098942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell-cell signaling from postsynapse to presynapse, across the synaptic cleft, mediated by trans-synaptic protein complex.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retrograde trans-synaptic signaling","termid":"GO:0098917"},{"relation_name":"is_a","term_name":"trans-synaptic signaling by trans-synaptic complex","termid":"GO:0099545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"retrograde trans-synaptic signaling by trans-synaptic protein complex","termid":"GO:0098942"}


id: GO:0140790
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: histone serine phosphate + H2O = histone serine + phosphate, and histone threonine phosphate + H2O = histone threonine + phosphate.","definition_xrefs":["PMID:18614045"],"gene_count":0,"genotype_count":0,"name":"obsolete histone serine/threonine phosphatase activity (obsolete GO:0140790)","termid":"GO:0140790"}


id: PBO:0058179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4473","termid":"PBO:0058179"}


id: GO:0045651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of macrophage differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of myeloid leukocyte differentiation","termid":"GO:0002763"},{"relation_name":"is_a","term_name":"regulation of macrophage differentiation","termid":"GO:0045649"},{"relation_name":"positively_regulates","term_name":"macrophage differentiation","termid":"GO:0030225"}],"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 macrophage differentiation","synonyms":[{"name":"activation of macrophage differentiation","type":"narrow"},{"name":"stimulation of macrophage differentiation","type":"narrow"},{"name":"up regulation of macrophage differentiation","type":"exact"},{"name":"up-regulation of macrophage differentiation","type":"exact"},{"name":"upregulation of macrophage differentiation","type":"exact"}],"termid":"GO:0045651"}


id: MONDO:0016259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant mixed epithelial and mesenchymal tumor that arises from the uterine corpus. It usually affects elderly postmenopausal women and presents with vaginal bleeding. It is characterized by the presence of a malignant epithelial component that is usually glandular and a sarcomatous component.","definition_xrefs":["NCIT:C9180"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine body mixed cancer","termid":"MONDO:0002879"},{"relation_name":"is_a","term_name":"uterine carcinosarcoma","termid":"MONDO:0006485"}],"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":"carcinosarcoma of the corpus uteri","secondary_identifiers":["UMLS:C1704376","GARD:12335","Orphanet:213610","MEDGEN:316458"],"synonyms":[{"name":"body of uterus carcinosarcoma","type":"exact"},{"name":"carcinosarcoma of corpus uteri","type":"exact"},{"name":"carcinosarcoma of the corpus uteri","type":"exact"},{"name":"carcinosarcoma of the uterine body","type":"exact"},{"name":"carcinosarcoma of the uterine corpus","type":"exact"},{"name":"carcinosarcoma of the uterus","type":"narrow"},{"name":"carcinosarcoma of uterine body","type":"exact"},{"name":"carcinosarcoma of uterine corpus","type":"exact"},{"name":"carcinosarcoma of uterus","type":"exact"},{"name":"corpus uteri malignant mixed mesodermal tumor","type":"exact"},{"name":"corpus uteri malignant mixed mesodermal tumour","type":"exact"},{"name":"malignant mixed Mullerian tumor of the corpus uteri","type":"exact"},{"name":"malignant mixed Mullerian tumour of the corpus uteri","type":"exact"},{"name":"malignant mixed Müllerian tumor of the corpus uteri","type":"exact"},{"name":"malignant mixed Müllerian tumour of the corpus uteri","type":"exact"},{"name":"malignant mixed mesodermal neoplasm of the uterine body","type":"exact"},{"name":"malignant mixed mesodermal neoplasm of the uterine corpus","type":"exact"},{"name":"malignant mixed mesodermal neoplasm of the uterus","type":"exact"},{"name":"malignant mixed mesodermal neoplasm of uterine body","type":"exact"},{"name":"malignant mixed mesodermal neoplasm of uterine corpus","type":"exact"},{"name":"malignant mixed mesodermal neoplasm of uterus","type":"exact"},{"name":"malignant mixed mesodermal tumor of the uterine body","type":"exact"},{"name":"malignant mixed mesodermal tumor of the uterine corpus","type":"exact"},{"name":"malignant mixed mesodermal tumor of the uterus","type":"exact"},{"name":"malignant mixed mesodermal tumor of uterine body","type":"exact"},{"name":"malignant mixed mesodermal tumor of uterine corpus","type":"exact"},{"name":"malignant mixed mesodermal tumor of uterus","type":"exact"},{"name":"malignant mixed mesodermal tumour of the uterine body","type":"exact"},{"name":"malignant mixed mesodermal tumour of the uterine corpus","type":"exact"},{"name":"malignant mixed mesodermal tumour of the uterus","type":"exact"},{"name":"malignant mixed mesodermal tumour of uterine body","type":"exact"},{"name":"malignant mixed mesodermal tumour of uterine corpus","type":"exact"},{"name":"malignant mixed mesodermal tumour of uterus","type":"exact"},{"name":"malignant mixed müllerian tumor of corpus uteri","type":"related"},{"name":"malignant mixed müllerian tumour of corpus uteri","type":"related"},{"name":"mixed Mullerian cancer of corpus uteri","type":"exact"},{"name":"mixed Mullerian sarcoma of the uterus","type":"exact"},{"name":"mixed Mullerian sarcoma of uterus","type":"exact"},{"name":"mixed Müllerian cancer of corpus uteri","type":"exact"},{"name":"mixed Müllerian sarcoma of the uterus","type":"exact"},{"name":"mixed Müllerian sarcoma of uterus","type":"exact"},{"name":"uterine body carcinosarcoma","type":"exact"},{"name":"uterine body malignant mixed mesodermal neoplasm","type":"exact"},{"name":"uterine body malignant mixed mesodermal tumor","type":"exact"},{"name":"uterine body malignant mixed mesodermal tumour","type":"exact"},{"name":"uterine carcinosarcoma","type":"broad"},{"name":"uterine corpus carcinosarcoma","type":"exact"},{"name":"uterine corpus malignant mixed Mullerian neoplasm","type":"exact"},{"name":"uterine corpus malignant mixed Mullerian tumor","type":"exact"},{"name":"uterine corpus malignant mixed Mullerian tumour","type":"exact"},{"name":"uterine corpus malignant mixed Müllerian neoplasm","type":"exact"},{"name":"uterine corpus malignant mixed Müllerian tumor","type":"exact"},{"name":"uterine corpus malignant mixed Müllerian tumour","type":"exact"},{"name":"uterine corpus malignant mixed mesodermal (Mullerian) tumor","type":"exact"},{"name":"uterine corpus malignant mixed mesodermal (Mullerian) tumour","type":"exact"},{"name":"uterine corpus malignant mixed mesodermal (Müllerian) tumor","type":"exact"},{"name":"uterine corpus malignant mixed mesodermal (Müllerian) tumour","type":"exact"},{"name":"uterine corpus malignant mixed mesodermal neoplasm","type":"exact"},{"name":"uterine corpus malignant mixed mesodermal tumor","type":"exact"},{"name":"uterine corpus malignant mixed mesodermal tumour","type":"exact"},{"name":"uterine malignant mixed mesodermal neoplasm","type":"exact"},{"name":"uterine malignant mixed mesodermal tumor","type":"exact"},{"name":"uterine malignant mixed mesodermal tumour","type":"exact"},{"name":"uterine mixed Mullerian sarcoma","type":"exact"},{"name":"uterine mixed Müllerian sarcoma","type":"exact"}],"termid":"MONDO:0016259","xrefs":{"Monarch":{"xref_id":"0016259"}}}


id: PBO:0051806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQSEC3 antisense RNA 2","termid":"PBO:0051806"}


id: GO:0102281
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: formylaminopyrimidine + H2O = 4-amino-5-ammoniomethyl-2-methylpyrimidine + formate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete formylaminopyrimidine deformylase activity (obsolete GO:0102281)","termid":"GO:0102281"}


id: MONDO:0006534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type of physical urticarias (or hives) that appears when a person is sweating.","definition_xrefs":["EFO:1000679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical urticaria","termid":"MONDO:0006599"}],"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":"cholinergic urticaria","secondary_identifiers":["icd11.foundation:855107748","SCTID:73098005","DOID:14443","ICD10CM:L50.5","ICD9:708.5","MEDGEN:508939","Wikipedia:Cholinergic_urticaria","UMLS:C0152230"],"termid":"MONDO:0006534","xrefs":{"Monarch":{"xref_id":"0006534"}}}


id: GO:0006035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of cuticle chitin, a linear polysaccharide consisting of beta-(1->4)-linked N-acetyl-D-glucosamine residues, found in cuticles.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cuticle chitin biosynthetic process (obsolete GO:0006035)","synonyms":[{"name":"cuticle chitin anabolism","type":"exact"},{"name":"cuticle chitin biosynthesis","type":"exact"},{"name":"cuticle chitin formation","type":"exact"},{"name":"cuticle chitin synthesis","type":"exact"}],"termid":"GO:0006035"}


id: GO:1904233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of aconitate hydratase activity.","definition_xrefs":["GOC:BHF","GO_REF:0000059","GOC:rl","GOC:TermGenie","PMID:18160053"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of aconitate hydratase activity (obsolete GO:1904233)","synonyms":[{"name":"down regulation of aconitase activity","type":"exact"},{"name":"down regulation of aconitate hydratase activity","type":"exact"},{"name":"down regulation of cis-aconitase activity","type":"exact"},{"name":"down regulation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"exact"},{"name":"down regulation of citrate(isocitrate) hydro-lyase activity","type":"exact"},{"name":"down-regulation of aconitase activity","type":"exact"},{"name":"down-regulation of aconitate hydratase activity","type":"exact"},{"name":"down-regulation of cis-aconitase activity","type":"exact"},{"name":"down-regulation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"exact"},{"name":"down-regulation of citrate(isocitrate) hydro-lyase activity","type":"exact"},{"name":"downregulation of aconitase activity","type":"exact"},{"name":"downregulation of aconitate hydratase activity","type":"exact"},{"name":"downregulation of cis-aconitase activity","type":"exact"},{"name":"downregulation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"exact"},{"name":"downregulation of citrate(isocitrate) hydro-lyase activity","type":"exact"},{"name":"inhibition of aconitase activity","type":"narrow"},{"name":"inhibition of aconitate hydratase activity","type":"narrow"},{"name":"inhibition of cis-aconitase activity","type":"narrow"},{"name":"inhibition of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"narrow"},{"name":"inhibition of citrate(isocitrate) hydro-lyase activity","type":"narrow"},{"name":"negative regulation of aconitase activity","type":"exact"},{"name":"negative regulation of cis-aconitase activity","type":"exact"},{"name":"negative regulation of citrate(isocitrate) hydro-lyase (cis-aconitate-forming)","type":"exact"},{"name":"negative regulation of citrate(isocitrate) hydro-lyase activity","type":"exact"}],"termid":"GO:1904233"}


id: GO:0051847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any mechanism of active immune avoidance which works by regulating the symbiont complement system, e.g. by possessing complement receptors which mediate attachment to, then infection of, symbiont macrophages, which are eventually destroyed. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","gene_count":0,"genotype_count":0,"name":"obsolete active evasion of symbiont immune response via regulation of symbiont complement system (obsolete GO:0051847)","synonyms":[{"name":"active evasion of symbiont immune response via regulation of symbiont complement system","type":"exact"},{"name":"active immune evasion via modulation of symbiont complement system","type":"exact"},{"name":"active immune evasion via regulation of symbiont complement system","type":"exact"}],"termid":"GO:0051847"}


id: GO:0000749
data:
  {"annotated_genes":["SJAG_03209","SJAG_00993","SJAG_01978","SJAG_00990","SJAG_01345","SJAG_01718","SJAG_03340","SJAG_02923"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107471],"is_not":false,"summary":null,"term":"GO:0000749"},{"annotations":[108233,65812,95205,98288,98956,91103],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071507"},{"annotations":[72464],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000750"}]},"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 pheromone stimulus that positively regulates the process of conjugation with cellular fusion. An example of this process is found in Saccharomyces cerevisiae.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to pheromone","termid":"GO:0071444"},{"relation_name":"positively_regulates","term_name":"conjugation with cellular fusion","termid":"GO:0000747"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00990":null,"SJAG_00993":null,"SJAG_01345":null,"SJAG_01718":null,"SJAG_01978":null,"SJAG_02923":null,"SJAG_03209":null,"SJAG_03340":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0000747"},{"rel_name":"positively_regulates","termid":"GO:0000747"}],"interesting_parent_ids":["GO:0008150","GO:0000747"],"is_obsolete":false,"name":"response to pheromone triggering conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0007328","GO:0030434"],"synonyms":[{"name":"response to pheromone during conjugation with cellular fusion","type":"related"}],"termid":"GO:0000749","terms_by_termid":{"GO:0000749":null,"GO:0000750":null,"GO:0071507":null}}


id: GO:0052880
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a diphenol, or related compound, acts as a hydrogen or electron donor and reduces a copper protein.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on diphenols and related substances as donors","termid":"GO:0016679"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"oxidoreductase activity, acting on diphenols and related substances as donors, with copper protein as acceptor","secondary_identifiers":["EC:1.10.9.-"],"termid":"GO:0052880"}


id: MONDO:0012732
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":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tremor, hereditary essential, and idiopathic normal pressure hydrocephalus","secondary_identifiers":["MESH:C567519","OMIM:611808","UMLS:C2678494","MEDGEN:394839"],"synonyms":[{"name":"ETINPH","type":"related"},{"name":"tremor, hereditary essential, and idiopathic normal pressure hydrocephalus","type":"exact"}],"termid":"MONDO:0012732","xrefs":{"Monarch":{"xref_id":"0012732"}}}


id: PBO:0017655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial aminoacyl-tRNA hydrolase Pth2 (predicted)","termid":"PBO:0017655"}


id: GO:1900157
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of bone mineralization involved in bone maturation.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of bone mineralization","termid":"GO:0030500"},{"relation_name":"regulates","term_name":"bone mineralization involved in bone maturation","termid":"GO:0035630"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of bone mineralization involved in bone maturation","termid":"GO:1900157"}


id: PR:Q9HGP7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC212.08c gene.","definition_xrefs":["UniProtKB:Q9HGP7","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 GPI-anchored protein C212.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC212.08c","synonyms":[{"name":"Spom972h-SPAC212.08c","type":"exact"}],"termid":"PR:Q9HGP7"}


id: GO:1905512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of short-term synaptic potentiation.","definition_xrefs":["GO_REF:0000058","GOC:hjd","GOC:TermGenie","PMID:15470145"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synaptic plasticity","termid":"GO:0048167"},{"relation_name":"regulates","term_name":"short-term synaptic potentiation","termid":"GO:1990926"}],"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 short-term synaptic potentiation","synonyms":[{"name":"regulation of synaptic facilitation","type":"exact"}],"termid":"GO:1905512"}


id: PBO:0047307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fas cell surface death receptor","termid":"PBO:0047307"}


id: GO:0050101
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-mimosine + H2O = 3-hydroxy-4H-pyrid-4-one + L-serine.","definition_xrefs":["RHEA:75355","GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amine-lyase activity","termid":"GO:0016843"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"mimosinase activity","secondary_identifiers":["KEGG_REACTION:R04350","EC:4.3.3.8","MetaCyc:MIMOSINASE-RXN"],"synonyms":[{"name":"mimosine amidohydrolase activity","type":"related"}],"termid":"GO:0050101"}


id: GO:0043367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized T cell acquires specialized features of a mature CD4-positive, alpha-beta T cell.","definition_xrefs":["ISBN:0781735149","CL:0000624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CD4-positive, alpha-beta T cell activation","termid":"GO:0035710"},{"relation_name":"is_a","term_name":"alpha-beta T cell differentiation","termid":"GO:0046632"}],"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":"CD4-positive, alpha-beta T cell differentiation","synonyms":[{"name":"CD4-positive, alpha beta T cell development","type":"related"},{"name":"CD4-positive, alpha beta T cell differentiation","type":"exact"},{"name":"CD4-positive, alpha-beta T lymphocyte differentiation","type":"exact"},{"name":"CD4-positive, alpha-beta T-cell differentiation","type":"exact"},{"name":"CD4-positive, alpha-beta T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0043367"}


id: GO:0070518
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha4-beta1 integrin complex bound to membrane protein CD53, a member of the tetraspan family.","definition_xrefs":["PMID:8757325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"alpha4-beta1 integrin-CD53 complex","synonyms":[{"name":"ITGA4-ITGB1-CD53 complex","type":"narrow"}],"termid":"GO:0070518"}


id: MONDO:0000182
data:
  {"annotated_genes":["SJAG_04728","SJAG_03056","SJAG_00924"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012518"},{"annotations":[87998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013883"},{"annotations":[87235],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014543"}]},"cv_name":"mondo","definition":"A congenital myasthenic syndrome with a finding of tubular aggregates in myofibers.","definition_xrefs":["PMID:21975507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"congenital myasthenic syndrome","termid":"MONDO:0018940"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00924":null,"SJAG_03056":null,"SJAG_04728":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital myasthenic syndrome with tubular aggregates","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:610542"],"synonyms":[{"name":"CMS-TA","type":"exact"},{"name":"myasthenic syndrome, congenital, with tubular aggregates","type":"exact"}],"termid":"MONDO:0000182","terms_by_termid":{"MONDO:0012518":null,"MONDO:0013883":null,"MONDO:0014543":null},"xrefs":{"Monarch":{"xref_id":"0000182"}}}


id: GO:0097013
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a phagocytic vesicle.","definition_xrefs":["GOC:rs"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocytic vesicle lumen","termid":"GO:0071682"},{"relation_name":"part_of","term_name":"phagocytic vesicle","termid":"GO:0045335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"phagocytic vesicle lumen","termid":"GO:0097013"}


id: PBO:0048503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth differentiation factor 3","termid":"PBO:0048503"}


id: PBO:0004563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L38 (predicted)","termid":"PBO:0004563"}


id: PBO:0090407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial rhomboid family protease","termid":"PBO:0090407"}


id: _global:level_fluctuates_during
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD_extension_relations","definition":"Identifies a biological phase or process during which the modification site occupancy is observed to vary.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"level_fluctuates_during","synonyms":[{"name":"occupancy_fluctuates_during","type":"exact"}],"termid":"_global:level_fluctuates_during"}


id: GO:0033229
data:
  {"annotated_genes":["SJAG_04295"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77208],"is_not":false,"summary":null,"term":"GO:0033229"}]},"cv_name":"molecular_function","definition":"Enables the transfer of cysteine from one side of a membrane to the other.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur amino acid transmembrane transporter activity","termid":"GO:0000099"},{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04295":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"cysteine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0033229","terms_by_termid":{"GO:0033229":null}}


id: PBO:0074643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 35B","termid":"PBO:0074643"}


id: GO:0071649
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of production of chemokine (C-C motif) ligand 5.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemokine production","termid":"GO:0032642"},{"relation_name":"regulates","term_name":"chemokine (C-C motif) ligand 5 production","termid":"GO:0071609"}],"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 chemokine (C-C motif) ligand 5 production","synonyms":[{"name":"regulation of CCL5 production","type":"exact"},{"name":"regulation of RANTES production","type":"exact"},{"name":"regulation of Regulated upon Activation, Normal T-cell Expressed, and Secreted production","type":"exact"}],"termid":"GO:0071649"}


id: MONDO:0042451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammation of the endometrium and the myometrium.","definition_xrefs":["Wikipedia:Endometritis#cite_note-isbn0-7817-5532-8-2","ISBN-13:978-0-7817-5532-0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyometritis","termid":"MONDO:0000497"},{"relation_name":"is_a","term_name":"endometritis","termid":"MONDO:0000918"},{"relation_name":"is_a","term_name":"adenomyosis","termid":"MONDO:0010888"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endomyometritis","secondary_identifiers":["MEDGEN:75710","SCTID:88027004","UMLS:C0269050","icd11.foundation:229826357"],"synonyms":[{"name":"endomyometritis","type":"exact"}],"termid":"MONDO:0042451","xrefs":{"Monarch":{"xref_id":"0042451"}}}


id: GO:2000502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of natural killer cell chemotaxis.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lymphocyte chemotaxis","termid":"GO:1901624"},{"relation_name":"is_a","term_name":"regulation of natural killer cell chemotaxis","termid":"GO:2000501"},{"relation_name":"negatively_regulates","term_name":"natural killer cell chemotaxis","termid":"GO:0035747"}],"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 natural killer cell chemotaxis","termid":"GO:2000502"}


id: PBO:0087285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Signal recognition particle (SRP) subunit (homolog of mammalian SRP54); contains the signal sequence-binding activity of SRP, interacts with the SRP RNA, and mediates binding of SRP to signal receptor; contains GTPase domain","termid":"PBO:0087285"}


id: MONDO:0033369
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 60","secondary_identifiers":["UMLS:C4693663","MEDGEN:1638894","OMIM:617929","DOID:0080432","GARD:16270"],"synonyms":[{"name":"DEE60","type":"exact"},{"name":"EIEE60","type":"exact"},{"name":"developmental and epileptic encephalopathy 60","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 60","type":"exact"}],"termid":"MONDO:0033369","xrefs":{"Monarch":{"xref_id":"0033369"}}}


id: GO:0061873
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hepatic stellate cell contraction.","definition_xrefs":["PMID:24204762"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament-based movement","termid":"GO:1903115"},{"relation_name":"regulates","term_name":"hepatic stellate cell contraction","termid":"GO:0061872"}],"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 hepatic stellate cell contraction","termid":"GO:0061873"}


id: MONDO:0004373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A papillary meningioma occurring in adults.","definition_xrefs":["NCIT:C8293"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhabdoid meningioma","termid":"MONDO:0003262"},{"relation_name":"is_a","term_name":"papillary meningioma","termid":"MONDO:0021088"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adult papillary meningioma","secondary_identifiers":["DOID:7826","UMLS:C0281334","MEDGEN:76256"],"synonyms":[{"name":"adult papillary meningioma","type":"exact"},{"name":"papillary meningioma","type":"broad"},{"name":"papillary meningioma of adults","type":"exact"}],"termid":"MONDO:0004373","xrefs":{"Monarch":{"xref_id":"0004373"}}}


id: PBO:0069722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1003, pseudogene","termid":"PBO:0069722"}


id: MONDO:0007315
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cherubism is a rare, self-limiting, fibro-osseous, genetic disease of childhood and adolescence characterized by varying degrees of progressive bilateral enlargement of the mandible and/or maxilla, with clinical repercussions in severe cases.","definition_xrefs":["Orphanet:184"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"cherubism","secondary_identifiers":["MEDGEN:40219","ICD9:526.89","MESH:D002636","NCIT:C84630","GARD:6036","NANDO:2200444","MedDRA:10070535","icd11.foundation:1729261719","OMIM:118400","SCTID:76098004","UMLS:C0008029","DOID:1856"],"synonyms":[{"name":"CRBM","type":"exact"},{"name":"Crbm","type":"related"},{"name":"cherubism","type":"exact"},{"name":"familial fibrous dysplasia of the jaws","type":"exact"},{"name":"familial multilocular cystic disease of the jaws","type":"exact"}],"termid":"MONDO:0007315","xrefs":{"Monarch":{"xref_id":"0007315"}}}


id: PBO:0002903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RFC related checkpoint protein Rad17","termid":"PBO:0002903"}


id: PBO:0057698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1286","termid":"PBO:0057698"}


id: GO:0140270
data:
  {"annotated_genes":["SJAG_04905"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94373],"is_not":false,"summary":null,"term":"GO:0140270"}]},"cv_name":"biological_process","definition":"The directed movement of gluconate from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:10735857"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gluconate transmembrane transport","termid":"GO:0035429"},{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04905":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"gluconate import across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140270","terms_by_termid":{"GO:0140270":null}}


id: GO:0006360
data:
  {"annotated_genes":["SJAG_03956","SJAG_00943","SJAG_05187","SJAG_00512","SJAG_01744","SJAG_01712","SJAG_04855","SJAG_02813","SJAG_00692","SJAG_00202","SJAG_04106","SJAG_01149","SJAG_02922","SJAG_04261","SJAG_02101","SJAG_01765","SJAG_02871","SJAG_03578","SJAG_03144","SJAG_03897","SJAG_03931","SJAG_01764","SJAG_01444","SJAG_00139","SJAG_02608","SJAG_04766","SJAG_00421","SJAG_01562","SJAG_00731","SJAG_02070","SJAG_02653","SJAG_01698","SJAG_01313","SJAG_04083","SJAG_02747","SJAG_05331","SJAG_01128","SJAG_03689","SJAG_04257","SJAG_03468"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[64223,80503,107224,110057,116542],"is_not":false,"summary":null,"term":"GO:0006360"},{"annotations":[77494,81024,81655,60018,80962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042790"},{"annotations":[74937,81263,78118,79814,80324],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045943"},{"annotations":[110372],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006356"},{"annotations":[79270,65019,69881],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001188"},{"annotations":[116215,117990,98293,104211],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006363"},{"annotations":[66131,69187,117531,116216,58367,71858,107745,65193,76954,97115,76302,105275,106834,65031,93919,79272,62793],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006362"},{"annotations":[73290,97479,109644,80964,73849,63345,95056,111714],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006361"}]},"cv_name":"biological_process","definition":"The synthesis of RNA from a DNA template by RNA polymerase I (RNAP I), originating at an RNAP I promoter.","definition_xrefs":["GOC:jl","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription","termid":"GO:0006351"}],"gene_count":40,"genes_by_uniquename":{"SJAG_00139":null,"SJAG_00202":null,"SJAG_00421":null,"SJAG_00512":null,"SJAG_00692":null,"SJAG_00731":null,"SJAG_00943":null,"SJAG_01128":null,"SJAG_01149":null,"SJAG_01313":null,"SJAG_01444":null,"SJAG_01562":null,"SJAG_01698":null,"SJAG_01712":null,"SJAG_01744":null,"SJAG_01764":null,"SJAG_01765":null,"SJAG_02070":null,"SJAG_02101":null,"SJAG_02608":null,"SJAG_02653":null,"SJAG_02747":null,"SJAG_02813":null,"SJAG_02871":null,"SJAG_02922":null,"SJAG_03144":null,"SJAG_03468":null,"SJAG_03578":null,"SJAG_03689":null,"SJAG_03897":null,"SJAG_03931":null,"SJAG_03956":null,"SJAG_04083":null,"SJAG_04106":null,"SJAG_04257":null,"SJAG_04261":null,"SJAG_04766":null,"SJAG_04855":null,"SJAG_05187":null,"SJAG_05331":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0006351","GO:0008150"],"is_obsolete":false,"name":"transcription by RNA polymerase I","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-73864"],"synonyms":[{"name":"RNA polymerase I transcription factor activity","type":"related"},{"name":"transcription from Pol I promoter","type":"exact"},{"name":"transcription from RNA polymerase I promoter","type":"exact"}],"termid":"GO:0006360","terms_by_termid":{"GO:0001188":null,"GO:0006356":null,"GO:0006360":null,"GO:0006361":null,"GO:0006362":null,"GO:0006363":null,"GO:0042790":null,"GO:0045943":null}}


id: PBO:0049002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol-3-phosphate dehydrogenase 1","termid":"PBO:0049002"}


id: GO:0016545
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process during courtship where the male insect vibrates his wings. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mtg_sensu","PMID:11092827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male courtship behavior, veined wing extension","termid":"GO:0048065"}],"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":"male courtship behavior, veined wing vibration","synonyms":[{"name":"male courtship behavior, wing vibration","type":"related"},{"name":"male courtship behaviour, veined wing vibration","type":"exact"},{"name":"male courtship behaviour, wing vibration","type":"related"}],"termid":"GO:0016545"}


id: MONDO:0019837
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete atrial appendage anomaly (obsolete MONDO:0019837)","secondary_identifiers":["Orphanet:95510"],"synonyms":[{"name":"atrial auricle anomaly","type":"exact"}],"termid":"MONDO:0019837","xrefs":{"Monarch":{"xref_id":"0019837"}}}


id: MONDO:1010862
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lysosomal storage disease that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease, non-human animal","termid":"MONDO:1010171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysosomal storage disease, cattle","secondary_identifiers":["OMIA:000616-9913"],"termid":"MONDO:1010862","xrefs":{"Monarch":{"xref_id":"1010862"}}}


id: MONDO:0009202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary lethal multiple congenital anomalies/dysmorphic syndrome","termid":"MONDO:0043009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Thakker-Donnai syndrome","secondary_identifiers":["GARD:5158","MEDGEN:346465","Orphanet:1780","UMLS:C1856892","MESH:C536503","OMIM:227255"],"synonyms":[{"name":"Dysmorphism multiple structural anomalies","type":"related"},{"name":"Dysmorphism-multiple structural anomalies syndrome","type":"exact"},{"name":"dysmorphic facial features and multiple structural abnormalities","type":"related"},{"name":"facial dysmorphism with multiple malformations","type":"related"}],"termid":"MONDO:0009202","xrefs":{"Monarch":{"xref_id":"0009202"}}}


id: PBO:0017864
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/ RNA polymerase II transcription factor Reb1","termid":"PBO:0017864"}


id: PBO:0057649
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1244-2","termid":"PBO:0057649"}


id: PATO:0001131
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001131 absolute ratio value (obsolete PATO:0001131)","termid":"PATO:0001131"}


id: MONDO:0100160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute disease characterized by severe ketoacidosis in the absence of diabetes mellitus and occurring in individuals with a history of prolonged excessive alcohol consumption. Disease manifestations include nausea, intractable vomiting, and abdominal pain. When treated, AKA resolves rapidly and completely with no apparent sequelae.","definition_xrefs":["PMID:16714496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acidosis disorder","termid":"MONDO:0006022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"alcoholic ketoacidosis","secondary_identifiers":["MEDGEN:541151","UMLS:C0268039","DOID:0080949"],"synonyms":[{"name":"alcoholic acidosis","type":"exact"},{"name":"alcoholic ketosis","type":"exact"}],"termid":"MONDO:0100160","xrefs":{"Monarch":{"xref_id":"0100160"}}}


id: PATO:0001281
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of purple color and high saturation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purple","termid":"PATO:0000951"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"saturated purple","synonyms":[{"name":"bright purple","type":"related"}],"termid":"PATO:0001281"}


id: FYPO:0002921
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 ubiquitination is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone modification during vegetative growth","termid":"FYPO:0000330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0002494","FYPO:0001320","FYPO:0002274","FYPO:0005447"],"is_obsolete":false,"name":"abnormal histone ubiquitination during vegetative growth","synonyms":[{"name":"abnormal histone ubiquitination during mitotic cell cycle","type":"related"},{"name":"abnormal histone ubiquitinylation during vegetative growth","type":"exact"},{"name":"abnormal histone ubiquitylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002921"}


id: PBO:0031174
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitotic_catastrophe_with_cut,_small_cell","termid":"PBO:0031174"}


id: PBO:0031121
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cell_population_growth_on_galactose_carbon_source","termid":"PBO:0031121"}


id: PBO:0076164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfatase 2","termid":"PBO:0076164"}


id: PBO:0070302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY1 pseudogene 8","termid":"PBO:0070302"}


id: PBO:0003081
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by Hsf1","termid":"PBO:0003081"}


id: PBO:0063749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 14","termid":"PBO:0063749"}


id: PBO:0079566
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin associated and SH3 domain containing A","termid":"PBO:0079566"}


id: GO:0060998
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of dendritic spine development, the process whose specific outcome is the progression of the dendritic spine over time, from its formation to the mature structure.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"dendritic spine development","termid":"GO:0060996"}],"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 dendritic spine development","termid":"GO:0060998"}


id: SO:0002218
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant in which the function of a gene product is altered with respect to a reference.","direct_ancestors":[{"relation_name":"is_a","term_name":"functional_effect_variant","termid":"SO:0001536"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally_abnormal","synonyms":[{"name":"function modified variant","type":"exact"},{"name":"function_modified_variant","type":"related"},{"name":"functionally abnormal","type":"related"}],"termid":"SO:0002218"}


id: GO:0035287
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Partitioning the insect head anlage into a fixed number of segmental units. The number of segments composing the insect head has long been a subject of debate, but it is generally agreed that there are 6 or 7 segments. From anterior to posterior the head segments are the procephalic segments (labral, (ocular), antennal and intercalary) and the gnathal segments (mandibular, maxillary and labial).","definition_xrefs":["PMID:10477305","PMID:7915837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification process","termid":"GO:0007389"},{"relation_name":"part_of","term_name":"blastoderm segmentation","termid":"GO:0007350"},{"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":"head segmentation","termid":"GO:0035287"}


id: GO:0061900
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change in morphology and behavior of a glial cell resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor.","definition_xrefs":["GOC:aruk","PMID:18723082","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell activation","termid":"GO:0001775"},{"relation_name":"part_of","term_name":"neuroinflammatory response","termid":"GO:0150076"}],"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":"glial cell activation","termid":"GO:0061900"}


id: GO:0009590
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a gravitational stimulus is received and converted into a molecular signal.","definition_xrefs":["GOC:dos","GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of external stimulus","termid":"GO:0009581"},{"relation_name":"is_a","term_name":"detection of abiotic stimulus","termid":"GO:0009582"},{"relation_name":"is_a","term_name":"response to gravity","termid":"GO:0009629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of gravity","synonyms":[{"name":"perception of gravity","type":"related"}],"termid":"GO:0009590"}


id: MONDO:0008183
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Annular pancreas is a distinct form of duodenal atresia in which the head of the pancreas forms a ring around the second portion of the duodenum.","definition_xrefs":["Orphanet:675"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreas disorder","termid":"MONDO:0002356"}],"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":"annular pancreas","secondary_identifiers":["MedDRA:10071757","MESH:C536376","MEDGEN:56211","GARD:705","icd11.foundation:1311285827","SCTID:40315008","OMIM:167750","ICD10CM:Q45.1","UMLS:C0149955","NCIT:C98813","DOID:0060850"],"synonyms":[{"name":"pancreas, annular","type":"related"}],"termid":"MONDO:0008183","xrefs":{"Monarch":{"xref_id":"0008183"}}}


id: PBO:0073715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-phase kinase associated protein 1 pseudogene 2","termid":"PBO:0073715"}


id: GO:0015217
data:
  {"annotated_genes":["SJAG_02050"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[59110],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005471"}]},"cv_name":"molecular_function","definition":"Enables the transfer of ADP, adenosine diphosphate, from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenine nucleotide transmembrane transporter activity","termid":"GO:0000295"},{"relation_name":"is_a","term_name":"purine ribonucleotide transmembrane transporter activity","termid":"GO:0005346"},{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02050":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"ADP transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:0015217","terms_by_termid":{"GO:0005471":null}}


id: MOD:01080
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:219"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acrylamidyl cysteinyl","synonyms":[{"name":"Acrylamidyl Cystenyl","type":"exact"}],"termid":"MOD:01080"}


id: GO:0072766
data:
  {"annotated_genes":["SJAG_02737","SJAG_02299","SJAG_05196","SJAG_00727","SJAG_01745"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91463,93221,104752,111939,118953],"is_not":false,"summary":null,"term":"GO:0072766"}]},"cv_name":"biological_process","definition":"The process in which chromatin, or kinetochores are anchored to the nuclear envelope. This process involves the microtubule cytoskeleton, and nuclear tethering factors and is responsible for the Rabl-like configuration of chromosomes in the interphase nuclei.","definition_xrefs":["PMID:23166349","GOC:mah","PMID:21965289","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome attachment to the nuclear envelope","termid":"GO:0097240"},{"relation_name":"is_a","term_name":"centromere clustering","termid":"GO:0098653"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00727":null,"SJAG_01745":null,"SJAG_02299":null,"SJAG_02737":null,"SJAG_05196":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"centromere clustering at the mitotic interphase nuclear envelope","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"centromere clustering at the mitotic nuclear envelope","type":"related"},{"name":"centromere clustering at the nuclear periphery","type":"broad"},{"name":"centromere-SPB clustering","type":"broad"},{"name":"kinetochore clustering at SPB","type":"broad"},{"name":"kinetochore clustering at spindle pole body","type":"broad"},{"name":"kinetochore clustering at the old mitotic spindle pole body","type":"exact"},{"name":"kinetochore localization at spindle pole body","type":"broad"},{"name":"rabl configuration","type":"related"}],"termid":"GO:0072766","terms_by_termid":{"GO:0072766":null}}


id: PBO:0000362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoesterase motif","termid":"PBO:0000362"}


id: MONDO:0021165
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm composed of large cells with large nuclei, prominent nucleoli, and abundant pale cytoplasm (Paget cells). Paget cell neoplasms include Paget disease of the nipple and extramammary Paget disease which may affect the vulva, penis, anus, skin and scrotum.","definition_xrefs":["NCIT:C7073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"Paget disease","secondary_identifiers":["MEDGEN:277958","UMLS:C1368019"],"synonyms":[{"name":"Paget cell neoplasm","type":"broad"},{"name":"Paget disease","type":"exact"},{"name":"Paget's cell neoplasm","type":"exact"},{"name":"Paget's disease","type":"exact"}],"termid":"MONDO:0021165","xrefs":{"Monarch":{"xref_id":"0021165"}}}


id: GO:0009109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of coenzymes, any of various nonprotein organic cofactors that are required, in addition to an enzyme and a substrate, for an enzymatic reaction to proceed.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete coenzyme catabolic process (obsolete GO:0009109)","synonyms":[{"name":"coenzyme and prosthetic group catabolic process","type":"broad"},{"name":"coenzyme and prosthetic group catabolism","type":"broad"},{"name":"coenzyme breakdown","type":"exact"},{"name":"coenzyme catabolism","type":"exact"},{"name":"coenzyme degradation","type":"exact"}],"termid":"GO:0009109"}


id: PBO:0002537
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"target of proteasome","termid":"PBO:0002537"}


id: PBO:0002433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Atf-CREB subfamily","termid":"PBO:0002433"}


id: FYPO:0005868
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of mitotic recombination is increased at ribosomal DNA.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased mitotic recombination","termid":"FYPO:0000473"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000293","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased mitotic recombination at rDNA","synonyms":[{"name":"increased mitotic recombination at rDNA during mitotic cell cycle","type":"related"},{"name":"increased mitotic recombination at rDNA during vegetative growth","type":"exact"},{"name":"increased mitotic recombination at ribosomal DNA","type":"exact"}],"termid":"FYPO:0005868"}


id: GO:1900428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of filamentous growth of a population of unicellular organisms.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of filamentous growth","termid":"GO:0010570"},{"relation_name":"regulates","term_name":"filamentous growth of a population of unicellular organisms","termid":"GO:0044182"}],"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 filamentous growth of a population of unicellular organisms","termid":"GO:1900428"}


id: MONDO:0019019
data:
  {"annotated_genes":["SJAG_02418","SJAG_02413","SJAG_00516","SJAG_00288","SJAG_02349","SJAG_04934","SJAG_00120","SJAG_01005","SJAG_04956"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018163"},{"annotations":[86987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013051"},{"annotations":[88540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007204"},{"annotations":[87266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014573"},{"annotations":[88335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012592"},{"annotations":[88097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009805"},{"annotations":[87530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030861"},{"annotations":[87967],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013889"},{"annotations":[87994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009910"},{"annotations":[87427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010208"}]},"cv_name":"mondo","definition":"Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterized by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity.","definition_xrefs":["Orphanet:666"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00120":null,"SJAG_00288":null,"SJAG_00516":null,"SJAG_01005":null,"SJAG_02349":null,"SJAG_02413":null,"SJAG_02418":null,"SJAG_04934":null,"SJAG_04956":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"osteogenesis imperfecta","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0029434","NCIT:C26837","OMIMPS:166200","SCTID:78314001","ICD9:756.51","icd11.foundation:1219932551","ICD10CM:Q78.0","DOID:12347","MedDRA:10031243","MESH:D010013","NANDO:1200873","NANDO:2201011","GARD:1017","MEDGEN:45246","NORD:1535"],"synonyms":[{"name":"Fragilitas ossium","type":"related"},{"name":"Lobstein disease","type":"exact"},{"name":"Lobstein's syndrome","type":"exact"},{"name":"OI","type":"exact"},{"name":"Osteopsathyrosis","type":"exact"},{"name":"Porak and Durante disease","type":"exact"},{"name":"Vrolik disease","type":"related"},{"name":"Vrolik's disease","type":"exact"},{"name":"brittle bone disease","type":"exact"},{"name":"glass bone disease","type":"exact"}],"termid":"MONDO:0019019","terms_by_termid":{"MONDO:0007204":null,"MONDO:0009805":null,"MONDO:0009910":null,"MONDO:0010208":null,"MONDO:0012592":null,"MONDO:0013051":null,"MONDO:0013889":null,"MONDO:0014573":null,"MONDO:0018163":null,"MONDO:0030861":null},"xrefs":{"Monarch":{"xref_id":"0019019"}}}


id: PBO:0001280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAMP complex ATP-dependent RNA helicase (predicted)","termid":"PBO:0001280"}


id: PBO:0036072
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_trimethylation_during_vegetative_growth","termid":"PBO:0036072"}


id: GO:0030023
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A component of the extracellular matrix that enables the matrix to recoil after transient stretching.","definition_xrefs":["ISBN:0815316194","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix structural constituent","termid":"GO:0005201"},{"relation_name":"is_a","term_name":"structural molecule activity conferring elasticity","termid":"GO:0097493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005198"}],"interesting_parent_ids":["GO:0003674","GO:0005198"],"is_obsolete":false,"name":"extracellular matrix constituent conferring elasticity","synonyms":[{"name":"core extracellular matrix","type":"broad"},{"name":"core matrisome","type":"broad"},{"name":"elastin","type":"related"}],"termid":"GO:0030023"}


id: PBO:0044520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DAB adaptor protein 1","termid":"PBO:0044520"}


id: MONDO:0021201
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory process affecting the skin, caused by bacteria, viruses, parasites, or fungi. Examples of bacterial infection include carbuncles, furuncles, impetigo, erysipelas, and abscesses. Examples of viral infection include shingles, warts, molluscum contagiosum, and pityriasis rosea. Examples of parasitic infection include scabies and lice. Examples of fungal infection include athlete's foot, yeast infection, and ringworm.","definition_xrefs":["NCIT:C35025"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatitis","termid":"MONDO:0002406"},{"relation_name":"is_a","term_name":"skin disorder caused by infection","termid":"MONDO:0024294"}],"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":"skin infection","secondary_identifiers":["MEDGEN:52365","SCTID:19824006","UMLS:C0037278"],"synonyms":[{"name":"skin infection","type":"exact"}],"termid":"MONDO:0021201","xrefs":{"Monarch":{"xref_id":"0021201"}}}


id: GO:0033147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the activity of an intracellular estrogen receptor signaling pathway.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of intracellular steroid hormone receptor signaling pathway","termid":"GO:0033144"},{"relation_name":"is_a","term_name":"regulation of intracellular estrogen receptor signaling pathway","termid":"GO:0033146"},{"relation_name":"negatively_regulates","term_name":"estrogen receptor signaling pathway","termid":"GO:0030520"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of intracellular estrogen receptor signaling pathway","synonyms":[{"name":"negative regulation of estrogen receptor signaling pathway","type":"broad"},{"name":"negative regulation of estrogen receptor signalling pathway","type":"exact"}],"termid":"GO:0033147"}


id: PATO:0002187
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Polar polarity is a quality that inheres in a molecular entity when the molecular entity is polar, i.e. does possess an electric dipole.","definition_xrefs":["PATOC:JH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polarity","termid":"PATO:0002186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polar polarity","termid":"PATO:0002187"}


id: GO:0061335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The growth of an epithelial cell dependent on cycles of endoreplication, where growth contributes to the shaping of the Malpighian tubule.","definition_xrefs":["GOC:dph","PMID:19783135","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental cell growth","termid":"GO:0048588"},{"relation_name":"is_a","term_name":"developmental growth involved in morphogenesis","termid":"GO:0060560"},{"relation_name":"part_of","term_name":"Malpighian tubule morphogenesis","termid":"GO:0007443"}],"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 growth involved in Malpighian tubule morphogenesis","termid":"GO:0061335"}


id: GO:1904578
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a thapsigargin stimulus.","definition_xrefs":["GO_REF:0000071","PMID:23106379","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete response to thapsigargin (obsolete GO:1904578)","termid":"GO:1904578"}


id: PBO:0062266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily G member 1 pseudogene","termid":"PBO:0062266"}


id: PBO:0000002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene characterisation status","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"biological role inferred","termid":"PBO:0000002"}


id: PBO:0002141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MTC tricarboxylate transporter (predicted)","termid":"PBO:0002141"}


id: PBO:0038917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor F5 pseudogene 1","termid":"PBO:0038917"}


id: PBO:0002636
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schneckenbecken dysplasia","termid":"PBO:0002636"}


id: PBO:0038778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activin A receptor type 1C","termid":"PBO:0038778"}


id: MONDO:0007461
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Short stature-valvular heart disease-characteristic facies syndrome is characterized by severe short stature with disproportionately short legs, small hands, clinodactyly, valvular heart disease and dysmorphism (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and two daughters. This syndrome is probably transmitted as an autosomal dominant trait.","definition_xrefs":["Orphanet:2868"],"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":"short stature-valvular heart disease-characteristic facies syndrome","secondary_identifiers":["GARD:16612","MEDGEN:338866","MESH:C565094","UMLS:C1852073","OMIM:126190"],"synonyms":[{"name":"disproportionate short stature with ptosis and valvular heart lesions","type":"related"}],"termid":"MONDO:0007461","xrefs":{"Monarch":{"xref_id":"0007461"}}}


id: MONDO:0020199
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete conjunctival vascular anomaly (obsolete MONDO:0020199)","secondary_identifiers":["Orphanet:98611"],"termid":"MONDO:0020199","xrefs":{"Monarch":{"xref_id":"0020199"}}}


id: GO:1900826
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of membrane depolarization during a cardiac muscle cell action potential.","definition_xrefs":["GOC:TermGenie","GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane depolarization during cardiac muscle cell action potential","termid":"GO:1900825"},{"relation_name":"is_a","term_name":"negative regulation of membrane depolarization","termid":"GO:1904180"},{"relation_name":"negatively_regulates","term_name":"membrane depolarization during cardiac muscle cell action potential","termid":"GO:0086012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of membrane depolarization during cardiac muscle cell action potential","synonyms":[{"name":"down regulation of membrane depolarization during cardiac muscle cell action potential","type":"exact"},{"name":"down-regulation of membrane depolarization during of cardiac muscle cell action potential","type":"exact"},{"name":"downregulation of membrane depolarization during cardiac muscle cell action potential","type":"exact"},{"name":"inhibition of membrane depolarization during cardiac muscle cell action potential","type":"narrow"}],"termid":"GO:1900826"}


id: GO:0085004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An interaction with the host organism mediated by a substance released by the other (symbiont) organism via the haustorium, a projection from a cell or tissue that penetrates the host's cell wall. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete interaction with host via secreted substance released from haustorium (obsolete GO:0085004)","termid":"GO:0085004"}


id: FYPO:0002354
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 protein encoded by heterochromatic genes that are normally silenced is higher than normal.","definition_xrefs":["PomBase:mah","PMID:22683269"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0006551","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased level of heterochromatin-encoded proteins","synonyms":[{"name":"increased level of heterochromatin-encoded proteins during mitotic cell cycle","type":"related"},{"name":"increased level of heterochromatin-encoded proteins during vegetative growth","type":"exact"}],"termid":"FYPO:0002354"}


id: PBO:0051730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrator complex subunit 3","termid":"PBO:0051730"}


id: GO:0015101
data:
  {"annotated_genes":["SJAG_00015","SJAG_04725","SJAG_02113","SJAG_00763","SJAG_01589","SJAG_03808","SJAG_00626","SJAG_06598","SJAG_02062","SJAG_04637","SJAG_00543","SJAG_04718","SJAG_04588","SJAG_02152","SJAG_02125","SJAG_00835","SJAG_04295","SJAG_00699","SJAG_04731","SJAG_02962","SJAG_02059","SJAG_00019","SJAG_02144","SJAG_03256","SJAG_02133","SJAG_04135","SJAG_02941","SJAG_04984","SJAG_04673","SJAG_02060","SJAG_03652","SJAG_03400","SJAG_01096","SJAG_02029","SJAG_01890"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58011,66503,120289,120290,120291,120292,120293,120294,120295,120484],"is_not":false,"summary":null,"term":"GO:0015101"},{"annotations":[113860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140485"},{"annotations":[117164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015220"},{"annotations":[77208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033229"},{"annotations":[79640,71826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015187"},{"annotations":[102603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034216"},{"annotations":[80919,99267,102283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061459"},{"annotations":[104737,112004],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015182"},{"annotations":[99268,80912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005290"},{"annotations":[112005,104738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015188"},{"annotations":[80916,112006,102284,104739,99269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015189"},{"annotations":[109868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000064"},{"annotations":[102276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015193"},{"annotations":[80917,92490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015194"},{"annotations":[80913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005302"},{"annotations":[101170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015200"},{"annotations":[72322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015489"},{"annotations":[92017,120785,119483,92018],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031925"},{"annotations":[120786,119484,92020,92019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031927"},{"annotations":[77919,81969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000095"},{"annotations":[112918,119361,72323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015606"},{"annotations":[105571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090422"},{"annotations":[92024,92023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015234"}]},"cv_name":"molecular_function","definition":"Enables the transfer of organic cations from one side of a membrane to the other. Organic cations are atoms or small molecules with a positive charge that contain carbon in covalent linkage.","definition_xrefs":["GOC:ai","GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":35,"genes_by_uniquename":{"SJAG_00015":null,"SJAG_00019":null,"SJAG_00543":null,"SJAG_00626":null,"SJAG_00699":null,"SJAG_00763":null,"SJAG_00835":null,"SJAG_01096":null,"SJAG_01589":null,"SJAG_01890":null,"SJAG_02029":null,"SJAG_02059":null,"SJAG_02060":null,"SJAG_02062":null,"SJAG_02113":null,"SJAG_02125":null,"SJAG_02133":null,"SJAG_02144":null,"SJAG_02152":null,"SJAG_02941":null,"SJAG_02962":null,"SJAG_03256":null,"SJAG_03400":null,"SJAG_03652":null,"SJAG_03808":null,"SJAG_04135":null,"SJAG_04295":null,"SJAG_04588":null,"SJAG_04637":null,"SJAG_04673":null,"SJAG_04718":null,"SJAG_04725":null,"SJAG_04731":null,"SJAG_04984":null,"SJAG_06598":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"organic cation transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-9794523","Reactome:R-HSA-561072","Reactome:R-HSA-9794270","Reactome:R-HSA-561054","Reactome:R-HSA-9795207","Reactome:R-HSA-549129","Reactome:R-HSA-549279","Reactome:R-HSA-549304","Reactome:R-HSA-2161500","Reactome:R-HSA-549322"],"termid":"GO:0015101","terms_by_termid":{"GO:0000064":null,"GO:0000095":null,"GO:0005290":null,"GO:0005302":null,"GO:0015101":null,"GO:0015182":null,"GO:0015187":null,"GO:0015188":null,"GO:0015189":null,"GO:0015193":null,"GO:0015194":null,"GO:0015200":null,"GO:0015220":null,"GO:0015234":null,"GO:0015489":null,"GO:0015606":null,"GO:0031925":null,"GO:0031927":null,"GO:0033229":null,"GO:0034216":null,"GO:0061459":null,"GO:0090422":null,"GO:0140485":null}}


id: MONDO:0019762
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Laryngo-tracheo-esophageal cleft (LC) type 2 is a congenital respiratory tract anomaly characterized by a cleft extending below the vocal folds into the cricoid cartilage, with swallowing disorders and lung infections.","definition_xrefs":["Orphanet:93939"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laryngotracheoesophageal cleft","termid":"MONDO:0016060"}],"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":"laryngotracheoesophageal cleft type 2","secondary_identifiers":["GARD:19237","MEDGEN:667240","UMLS:C0584824"],"synonyms":[{"name":"LTEC II","type":"exact"},{"name":"LTEC2","type":"exact"},{"name":"laryngo-tracheo-esophageal cleft type 2","type":"exact"}],"termid":"MONDO:0019762","xrefs":{"Monarch":{"xref_id":"0019762"}}}


id: GO:0044555
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency of heart contraction of another organism.","definition_xrefs":["PMID:20923766","GOC:jl","GOC:ecd"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of heart rate in another organism (obsolete GO:0044555)","synonyms":[{"name":"negative regulation of heart rate in other organism","type":"exact"}],"termid":"GO:0044555"}


id: PBO:0000802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA 5' exonuclease (predicted)","termid":"PBO:0000802"}


id: PBO:0054483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1883","termid":"PBO:0054483"}


id: FYPO:0004164
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of reactive oxygen species (ROS) measured in a cell is higher than normal when the population in which the cell is found is in stationary phase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered cellular reactive oxygen species level","termid":"FYPO:0002142"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular reactive oxygen species level in stationary phase","synonyms":[{"name":"increased ROS accumulation in stationary phase","type":"related"},{"name":"increased cellular ROS accumulation in stationary phase","type":"related"},{"name":"increased cellular ROS level in stationary phase","type":"exact"},{"name":"increased cellular reactive oxygen species accumulation in stationary phase","type":"related"}],"termid":"FYPO:0004164"}


id: PBO:0059589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ATP6 pseudogene 1","termid":"PBO:0059589"}


id: PBO:0045540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual oxidase maturation factor 2","termid":"PBO:0045540"}


id: MONDO:0001859
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex regional pain syndrome","termid":"MONDO:0019369"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"algoneurodystrophy","secondary_identifiers":["MEDGEN:526108","ICD10CM:M89.0","DOID:14022","UMLS:C0205930","ICD9:733.7"],"termid":"MONDO:0001859","xrefs":{"Monarch":{"xref_id":"0001859"}}}


id: GO:0072286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the metanephric connecting tubule over time, from its formation to the mature structure. The metanephric connecting tubule is a tubular segment of the metanephric nephron; it connects the distal convoluted tubule to the collecting duct in the metanephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connecting tubule development","termid":"GO:0072027"},{"relation_name":"is_a","term_name":"metanephric nephron tubule development","termid":"GO:0072234"}],"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 connecting tubule development","synonyms":[{"name":"metanephric connecting duct development","type":"exact"}],"termid":"GO:0072286"}


id: MONDO:0016092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Serous or mucinous cystadenoma of childhood is a benign epithelial ovarian tumor characterized by a usually unilateral, cystic, unilocular or multilocular lesion with a thin wall or septa and no intracystic solid portion on imaging. It often presents with abdominal pain or an asymptomatic abdominal mass and can be associated with ovarian torsion or malignant transformation.","definition_xrefs":["Orphanet:206470"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian benign neoplasm","termid":"MONDO:0000646"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serous or mucinous cystadenoma of childhood","secondary_identifiers":["GARD:20346","MEDGEN:1803886","UMLS:C5679785"],"synonyms":[{"name":"mucinous cystadenoma of ovary in childhood","type":"exact"},{"name":"serous cystadenoma of ovary in childhood","type":"exact"}],"termid":"MONDO:0016092","xrefs":{"Monarch":{"xref_id":"0016092"}}}


id: MONDO:0044342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any degenerative disorder affecting one or more vertebral disks of the thoracic spine.","definition_xrefs":["NCIT:C27155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intervertebral disk degenerative disorder","termid":"MONDO:0011385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thoracic disk degenerative disorder","secondary_identifiers":["SCTID:68675004","UMLS:C0263872","MEDGEN:120491"],"synonyms":[{"name":"degeneration of thoracic intervertebral disc","type":"exact"},{"name":"degeneration of thoracic intervertebral disk","type":"exact"},{"name":"intervertebral disc degenerative disorder of thoracic region of vertebral column","type":"exact"},{"name":"intervertebral disk degenerative disorder of thoracic region of vertebral column","type":"exact"},{"name":"thoracic Disc Degeneration","type":"exact"},{"name":"thoracic Disc degenerative disease","type":"exact"},{"name":"thoracic Disc degenerative disorder","type":"exact"},{"name":"thoracic region of vertebral column intervertebral disc degenerative disorder","type":"exact"},{"name":"thoracic region of vertebral column intervertebral disk degenerative disorder","type":"exact"}],"termid":"MONDO:0044342","xrefs":{"Monarch":{"xref_id":"0044342"}}}


id: MONDO:1010641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Factor XII deficiency that occurs in killer whale.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"factor XII deficiency, non-human animal","termid":"MONDO:1010074"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"factor XII deficiency, killer whale","secondary_identifiers":["OMIA:000364-9733"],"termid":"MONDO:1010641","xrefs":{"Monarch":{"xref_id":"1010641"}}}


id: GO:0160207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of androgen receptor signaling.","definition_xrefs":["PMID:29057879"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of intracellular steroid hormone receptor signaling pathway","termid":"GO:0033145"},{"relation_name":"is_a","term_name":"regulation of androgen receptor signaling pathway","termid":"GO:0060765"},{"relation_name":"positively_regulates","term_name":"androgen receptor signaling pathway","termid":"GO:0030521"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of androgen receptor signaling pathway","termid":"GO:0160207"}


id: RO:0002587
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"results_in_formation_of","termid":"_global:results_in_formation_of"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_synthesis_of","termid":"RO:0002587"}


id: PBO:0080991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 22","termid":"PBO:0080991"}


id: PR:O14170
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pop2 gene.","definition_xrefs":["UniProtKB:O14170","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":"WD repeat-containing protein pop2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.03","synonyms":[{"name":"Spom972h-pop2","type":"exact"},{"name":"proteolysis factor sud1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14170"}


id: GO:0035809
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the amount of urine excreted from the body over a unit of time.","definition_xrefs":["GOC:mtg_25march11","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal system process","termid":"GO:0003014"},{"relation_name":"is_a","term_name":"regulation of body fluid levels","termid":"GO:0050878"}],"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 urine volume","synonyms":[{"name":"regulation of urinary volume","type":"exact"},{"name":"regulation of urine flow","type":"exact"}],"termid":"GO:0035809"}


id: GO:0004957
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with prostaglandin E (PGE(2)) to initiate a change in cell activity.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostaglandin receptor activity","termid":"GO:0004955"}],"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":"prostaglandin E receptor activity","synonyms":[{"name":"PGE receptor activity","type":"related"},{"name":"PGE(2) receptor activity","type":"exact"}],"termid":"GO:0004957"}


id: GO:0060147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the inactivation of gene expression by a posttranscriptional mechanism.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gene expression","termid":"GO:0010468"},{"relation_name":"regulates","term_name":"post-transcriptional gene silencing","termid":"GO:0016441"}],"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 post-transcriptional gene silencing","synonyms":[{"name":"regulation of posttranscriptional gene silencing","type":"exact"}],"termid":"GO:0060147"}


id: PBO:0027144
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_mitotic_G2_DNA_damage_checkpoint","termid":"PBO:0027144"}


id: MONDO:0004333
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant, ectopic ACTH secreting pancreatic neuroendocrine tumor, associated with Cushing's syndrome. The prognosis is usually poor.","definition_xrefs":["NCIT:C27466"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functional pancreatic neuroendocrine tumor","termid":"MONDO:0023206"}],"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":"pancreatic ACTH-producing neuroendocrine tumor","secondary_identifiers":["MEDGEN:233302","UMLS:C1335300","DOID:7697","ICDO:8158/1"],"synonyms":[{"name":"pancreatic ACTH hormone producing tumor","type":"related"},{"name":"pancreatic ACTH hormone producing tumour","type":"related"},{"name":"pancreatic ACTH producing NET","type":"exact"},{"name":"pancreatic ACTH producing neuroendocrine tumor","type":"exact"},{"name":"pancreatic ACTH producing neuroendocrine tumour","type":"exact"},{"name":"pancreatic ACTH producing tumor","type":"exact"},{"name":"pancreatic ACTH producing tumour","type":"exact"},{"name":"pancreatic ACTH-producing neuroendocrine tumor","type":"exact"},{"name":"pancreatic adrenocorticotropic hormone producing tumor","type":"exact"},{"name":"pancreatic adrenocorticotropic hormone producing tumour","type":"exact"}],"termid":"MONDO:0004333","xrefs":{"Monarch":{"xref_id":"0004333"}}}


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":["MESH:D012295","MedDRA:10039143","MEDGEN:20589","SCTID:402917003","GARD:21416","DOID:1328","ICD10CM:A92.4","icd11.foundation:854137188","UMLS:C0035613","NCIT:C128419"],"synonyms":[{"name":"RVF","type":"exact"}],"termid":"MONDO:0017880","xrefs":{"Monarch":{"xref_id":"0017880"}}}


id: GO:0018988
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The periodic shedding of part or all of a protein-based cuticle, which is then replaced by a new protein-based cuticle. A cuticle is the outer layer of an animal which acts to prevent water loss.","definition_xrefs":["GOC:mtg_sensu","GOC:ems"],"gene_count":0,"genotype_count":0,"name":"obsolete molting cycle, protein-based cuticle (obsolete GO:0018988)","synonyms":[{"name":"protein-based cuticle molting cycle","type":"exact"}],"termid":"GO:0018988"}


id: PBO:0040558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B3GNTL1 pseudogene 1","termid":"PBO:0040558"}


id: GO:0102806
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-coumaryl-CoA + cyanin betaine = shisonin + coenzyme A.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4-coumaroyl-CoA:cyanidin-3,5-diglucoside-6''-O-acyltransferase activity (obsolete GO:0102806)","termid":"GO:0102806"}


id: MONDO:0013530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial atrial fibrillation in which the cause of the disease is a mutation in the SCN5A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial atrial fibrillation","termid":"MONDO:0018054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"atrial fibrillation, familial, 10","secondary_identifiers":["GARD:15745","OMIM:614022","UMLS:C3151464","MEDGEN:462814"],"synonyms":[{"name":"ATFB10","type":"related"},{"name":"SCN5A familial atrial fibrillation","type":"exact"},{"name":"atrial fibrillation, familial, 10","type":"exact"},{"name":"atrial fibrillation, familial, type 10","type":"exact"},{"name":"familial atrial fibrillation caused by mutation in SCN5A","type":"exact"}],"termid":"MONDO:0013530","xrefs":{"Monarch":{"xref_id":"0013530"}}}


id: PBO:0070154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 68 pseudogene","termid":"PBO:0070154"}


id: PBO:0046307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectodermal-neural cortex 1","termid":"PBO:0046307"}


id: GO:0016061
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of light-activated channel activity.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of light-activated channel activity (obsolete GO:0016061)","termid":"GO:0016061"}


id: PBO:0060095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 42","termid":"PBO:0060095"}


id: GO:0036182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving asperthecin, an anthraquinone pigment obtained from the mould Aspergillus nidulans.","definition_xrefs":["GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"asperthecin metabolic process","synonyms":[{"name":"asperthecin metabolism","type":"exact"}],"termid":"GO:0036182"}


id: PBO:0043154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 22","termid":"PBO:0043154"}


id: MONDO:0001767
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal apparatus disorder","termid":"MONDO:0001854"},{"relation_name":"is_a","term_name":"eyelid disorder","termid":"MONDO:0003382"}],"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":"stenosis of lacrimal punctum","secondary_identifiers":["MEDGEN:509869","DOID:13653","ICD9:375.52","SCTID:74783009","UMLS:C0155244"],"termid":"MONDO:0001767","xrefs":{"Monarch":{"xref_id":"0001767"}}}


id: GO:0018505
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cis-1,2-dihydronaphthalene-1,2-diol + NAD+ = naphthalene-1,2-diol + NADH + H+.","definition_xrefs":["EC:1.3.1.29"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"cis-1,2-dihydro-1,2-dihydroxynaphthalene dehydrogenase activity","secondary_identifiers":["MetaCyc:1.3.1.29-RXN","RHEA:11832"],"synonyms":[{"name":"(+)-cis-naphthalene dihydrodiol dehydrogenase activity","type":"related"},{"name":"1,2-dihydroxy-1,2-dihydroxynaphthalene dehydrogenase activity","type":"exact"},{"name":"cis-1,2-dihydronaphthalene-1,2-diol:NAD+ 1,2-oxidoreductase activity","type":"related"},{"name":"cis-dihydrodiol naphthalene dehydrogenase activity","type":"related"},{"name":"cis-naphthalene dihydrodiol dehydrogenase activity","type":"related"},{"name":"naphthalene dihydrodiol dehydrogenase activity","type":"related"}],"termid":"GO:0018505"}


id: PBO:0087527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of MRX complex with Mre11p and Xrs2p; complex is involved in processing double-strand DNA breaks in vegetative cells, initiation of meiotic DSBs, telomere maintenance, and nonhomologous end joining; forms nuclear foci upon DNA replication stress","termid":"PBO:0087527"}


id: PBO:0005540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3'(2'),5'-bisphosphate nucleotidase/inositol-1,4- bisphosphate 1-phosphatase","termid":"PBO:0005540"}


id: GO:0120166
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of producing fruiting body precursors, called protoperithecia. Protoperitheicium is a spherical structure that is formed in the sexual phase of ascomycetous fungi such as Neurospora crassa and Sordaria macrospora. Protoperithecium is formed by the enveloping of ascogonia cells by sterile hyphae and it develops into perithecium.","definition_xrefs":["PMID:6235211","PMID:6235212","DOI:10.1007/978-3-642-00286-1_2","PMID:125266","PMID:25311923","PMID:20739093","PMID:4410944"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive fruiting body development","termid":"GO:0030582"}],"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":"protoperithecium formation","termid":"GO:0120166"}


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


id: MONDO:0035238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare subtype of pyoderma gangrenosum disease characterized by a solitary, erythematous, ulcerated plaque, which lacks the violaceous border typically present in classic pyoderma gangrenosum, usually affecting individuals who are otherwise healthy. Histologically, the lesion presents a central layer containing neutrophilic inflammation, surrounded by a palisade of histiocytes, which are rimmed by a lymphocytic infiltrate. In comparison with the other variants of pyoderma gangrenosum, this subtype usually shows a good response to less aggressive treatments and underlying systemic disorders are less frequently associated. It is considered the most benign and uncommon clinical variant of pyoderma gangrenosum.","definition_xrefs":["Orphanet:538872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyoderma gangrenosum","termid":"MONDO:0018824"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"vegetative pyoderma gangrenosum","secondary_identifiers":["UMLS:C5680158","MEDGEN:1842944","GARD:22223","ICD10CM:L88"],"synonyms":[{"name":"Granulomatous pyoderma gangrenosum","type":"exact"}],"termid":"MONDO:0035238","xrefs":{"Monarch":{"xref_id":"0035238"}}}


id: FYPO:0002071
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which a cell has a nucleus in an abnormal location. The normal location of a single nucleus is at the midpoint of the long axis of the cell (during mitotic telophase, daughter nuclei normally move away from the cell division site).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular physical quality phenotype during vegetative growth","termid":"FYPO:0001321"},{"relation_name":"is_a","term_name":"mislocalized nucleus","termid":"FYPO:0002069"},{"relation_name":"output_of","term_name":"abnormal nucleus positioning during vegetative growth","termid":"FYPO:0001338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000138","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"mislocalized nucleus during vegetative growth","synonyms":[{"name":"abnormal nucleus location during vegetative growth","type":"exact"},{"name":"abnormal nucleus position during vegetative growth","type":"exact"},{"name":"displaced nucleus during vegetative growth","type":"exact"},{"name":"mislocalised nucleus during vegetative growth","type":"exact"},{"name":"mislocalized nucleus during mitotic cell cycle","type":"related"},{"name":"misplaced nuclei during vegetative growth","type":"exact"},{"name":"misplaced nucleus during vegetative growth","type":"exact"},{"name":"nuclear displacement during vegetative growth","type":"exact"}],"termid":"FYPO:0002071"}


id: PBO:0063929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoinositide kinase, FYVE-type zinc finger containing","termid":"PBO:0063929"}


id: PBO:0018162
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pombe SYntaxin-like protein","termid":"PBO:0018162"}


id: PBO:0053039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"La ribonucleoprotein 1B","termid":"PBO:0053039"}


id: MONDO:0001829
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A nerve plexus disease that involves the lumbosacral nerve plexus.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nerve plexus disorder","termid":"MONDO:0024432"}],"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":"lumbosacral plexus lesion","secondary_identifiers":["SCTID:4062006","ICD9:353.1","DOID:13913","UMLS:C0154735","MEDGEN:509637"],"synonyms":[{"name":"lumbosacral nerve plexus nerve plexus disease","type":"exact"},{"name":"lumbosacral plexus lesions","type":"exact"},{"name":"nerve plexus disease of lumbosacral nerve plexus","type":"exact"}],"termid":"MONDO:0001829","xrefs":{"Monarch":{"xref_id":"0001829"}}}


id: GO:0047456
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2S,3R)-3-hydroxybutane-1,2,3-tricarboxylate = cis-2-methylaconitate + H2O.","definition_xrefs":["EC:4.2.1.99","RHEA:17941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-methylisocitrate dehydratase activity","secondary_identifiers":["KEGG_REACTION:R04425","MetaCyc:4.2.1.99-RXN"],"synonyms":[{"name":"(2S,3R)-3-hydroxybutane-1,2,3-tricarboxylate hydro-lyase [(Z)-but-2-ene-1,2,3-tricarboxylate-forming]","type":"related"},{"name":"(2S,3R)-3-hydroxybutane-1,2,3-tricarboxylate hydro-lyase activity","type":"related"}],"termid":"GO:0047456"}


id: PBO:0077136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIR domain containing adaptor protein","termid":"PBO:0077136"}


id: GO:0097207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A dormancy process in which dormancy (sometimes called a dormant state) is induced, maintained or broken in a bud. Bud dormancy is a suspension of most physiological activity and growth that can be reactivated. It may be a response to environmental conditions such as seasonality or extreme heat, drought, or cold. The exit from bud dormancy is marked by the resumed growth of the bud.","definition_xrefs":["GOC:PO_curators","PO_REF:00009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dormancy process","termid":"GO:0022611"},{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"bud dormancy process","synonyms":[{"name":"bud dormancy","type":"related"}],"termid":"GO:0097207"}


id: GO:0005914
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small cell-cell adherens junction assembled during the cellularization stage of insect embyrogenesis; spot adherens junctions later fuse to form the zonula adherens.","definition_xrefs":["PMID:11700298"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adherens junction","termid":"GO:0005912"}],"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":"spot adherens junction","synonyms":[{"name":"dense plaque","type":"broad"},{"name":"punctum adherens","type":"exact"}],"termid":"GO:0005914"}


id: PBO:0067581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 738, pseudogene","termid":"PBO:0067581"}


id: GO:0015640
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of peptidoglycan peptides from one side of a membrane to the other. Peptidoglycan peptides are the oligopeptides found in peptidoglycan networks which cross-link the polysaccharide chains.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidoglycan transmembrane transporter activity","termid":"GO:0015647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"peptidoglycan peptide transmembrane transporter activity","synonyms":[{"name":"murein peptide transporter activity","type":"exact"},{"name":"muropeptide transporter activity","type":"exact"}],"termid":"GO:0015640"}


id: PBO:0081317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 101","termid":"PBO:0081317"}


id: PBO:0054701
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 2110","termid":"PBO:0054701"}


id: PBO:0056215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member B17","termid":"PBO:0056215"}


id: GO:0005427
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a oligopeptide from one side of a membrane to the other, up its concentration gradient. The transporter binds the solute and undergoes a series of conformational changes. Transport works equally well in either direction and is driven by proton movement.","definition_xrefs":["OMIM:600544","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary active transmembrane transporter activity","termid":"GO:0015291"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"proton-dependent oligopeptide secondary active transmembrane transporter activity","synonyms":[{"name":"hydrogen/oligopeptide symporter","type":"related"},{"name":"proton-dependent oligopeptide transporter activity","type":"exact"}],"termid":"GO:0005427"}


id: GO:1990173
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within the nucleoplasm.","definition_xrefs":["GOC:mah","PMID:22918952"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to nucleus","termid":"GO:0034504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to nucleoplasm","secondary_identifiers":["GO:0032066"],"synonyms":[{"name":"nucleolus to nucleoplasm transport","type":"related"},{"name":"protein localisation to nucleoplasm","type":"exact"}],"termid":"GO:1990173"}


id: MONDO:0100574
data:
  {"annotated_genes":["SJAG_03536"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88560],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014517"}]},"cv_name":"mondo","definition":"Epilepsy that is characterized by generalized seizure types and may have typical interictal and/or ictal EEG findings that accompany generalized seizure types (for example generalized spike-wave).","direct_ancestors":[{"relation_name":"is_a","term_name":"epilepsy","termid":"MONDO:0005027"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03536":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"generalized epilepsy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C3021","UMLS:C0014548","MEDGEN:4507"],"termid":"MONDO:0100574","terms_by_termid":{"MONDO:0014517":null},"xrefs":{"Monarch":{"xref_id":"0100574"}}}


id: PBO:0084546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the Puf family of RNA-binding proteins; interacts with mRNAs encoding membrane-associated proteins; involved in localizing the Arp2/3 complex to mitochondria; overexpression causes increased sensitivity to benomyl; JSN1 has a paralog, PUF2, that arose from the whole genome duplication","termid":"PBO:0084546"}


id: GO:0048769
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which sarcomeres are added in series within a fiber.","definition_xrefs":["GOC:jid","GOC:lm","PMID:15947030"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actomyosin structure organization","termid":"GO:0031032"},{"relation_name":"part_of","term_name":"myofibril assembly","termid":"GO:0030239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0030036","GO:0044085"],"is_obsolete":false,"name":"sarcomerogenesis","synonyms":[{"name":"myofibril production","type":"exact"}],"termid":"GO:0048769"}


id: PR:Q9UUF2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A methionine--tRNA ligase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02850","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":"methionine--tRNA ligase, cytoplasmic (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17A3.04c","secondary_identifiers":["UniProtKB:Q9UUF2"],"synonyms":[{"name":"MetRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-metG","type":"exact"},{"name":"methionyl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UUF2"}


